The acidity of atmospheric particles and clouds
- 1Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA
- 2School of Architecture, Civil and Environmental Engineering, Ecole Polytechnique Fédérale de Lausanne, Lausanne, 1015, Switzerland
- 3Institute for Chemical Engineering Sciences, Foundation for Research and Technology Hellas, Patras, 26504, Greece
- 4Department of Atmospheric Science, University of Washington, Seattle, WA 98195, USA
- 5Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USA
- 6National Center for Atmospheric Research, Boulder, CO 80307, USA
- 7School of Environmental Sciences, University of East Anglia, Norwich NR4 7TJ, UK
- 8Department of Atmospheric Science, Colorado State University, Fort Collins, CO 80523, USA
- 9Department of Chemical, Biochemical, and Environmental Engineering, University of Maryland, Baltimore County, Baltimore, MD 21250, USA
- 10Leibniz Institute for Tropospheric Research (TROPOS), Atmospheric Chemistry Department (ACD), 04318 Leipzig, Germany
- 11Environmental Chemical Processes Laboratory, Department of Chemistry, University of Crete, Voutes, Heraklion Crete, 71003, Greece
- 12Office of Air Quality Planning and Standards, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA
- 13Department of Chemical Engineering, Columbia University, New York, NY 10027, USA
- 14Department of Atmospheric Sciences, University of Illinois at Urbana-Champaign, Urbana-Champaign, Illinois 61801, USA
- 15State Environmental Protection Key Laboratory of Urban Ambient Air Particulate Matter Pollution Prevention and Control, Nankai University, Tianjin, 300071, China
- 16Department of Civil and Environmental Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China
- 17School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA 30332, USA
- 18School of Environment, Tsinghua University, Beijing, 100084, China
- 19Atmospheric Sciences & Global Change Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA
- 20Department of Atmospheric and Oceanic Sciences, McGill University, Montreal, Quebec, H3A 0B9, Canada
Correspondence: Havala O. T. Pye (firstname.lastname@example.org)
Acidity, defined as pH, is a central component of aqueous chemistry. In the atmosphere, the acidity of condensed phases (aerosol particles, cloud water, and fog droplets) governs the phase partitioning of semivolatile gases such as HNO3, NH3, HCl, and organic acids and bases as well as chemical reaction rates. It has implications for the atmospheric lifetime of pollutants, deposition, and human health. Despite its fundamental role in atmospheric processes, only recently has this field seen a growth in the number of studies on particle acidity. Even with this growth, many fine-particle pH estimates must be based on thermodynamic model calculations since no operational techniques exist for direct measurements. Current information indicates acidic fine particles are ubiquitous, but observationally constrained pH estimates are limited in spatial and temporal coverage. Clouds and fogs are also generally acidic, but to a lesser degree than particles, and have a range of pH that is quite sensitive to anthropogenic emissions of sulfur and nitrogen oxides, as well as ambient ammonia. Historical measurements indicate that cloud and fog droplet pH has changed in recent decades in response to controls on anthropogenic emissions, while the limited trend data for aerosol particles indicate acidity may be relatively constant due to the semivolatile nature of the key acids and bases and buffering in particles. This paper reviews and synthesizes the current state of knowledge on the acidity of atmospheric condensed phases, specifically particles and cloud droplets. It includes recommendations for estimating acidity and pH, standard nomenclature, a synthesis of current pH estimates based on observations, and new model calculations on the local and global scale.
Human activity and natural processes result in emissions of sulfur, nitrogen, ammonia, dust, and other compounds that affect the composition of the Earth's atmosphere. The acidity of suspended atmospheric media, particles and droplets, influences many processes that involve the atmosphere and all aspects of the Earth system (e.g., watersheds, marine and terrestrial ecosystems) that interface with it (see Fig. 1). Aerosols (also referred to as particulate matter, PM) and cloud droplets throughout the atmosphere exhibit a wide range of acidity, each spanning 5 orders of magnitude or more in molality units, or 5 units of pH (Fig. 2). Some anthropogenic emissions (sulfur dioxide, nitrogen oxides, organic acids) increase acidity while others (ammonia; nonvolatile cations, NVCs; amines) reduce acidity. The orders-of-magnitude differences in water content between aerosols and clouds lead to distinctly different acidity levels in these media, as well as their response to changes in precursor concentrations. The ability of a chemical species to affect particle or cloud droplet acidity is driven by both its degree of acidity (or basicity), reflected in the dissociation (or association) constant, and by volatility, with less volatile compounds partitioning to a greater degree into liquid aerosols and cloud droplets. Semivolatile species, for which significant fractions typically exist in both the gas and condensed phases, include ammonia (NH3), nitric acid (HNO3), hydrochloric acid (HCl), and low-molecular-weight organic acids (formic, acetic, oxalic, malonic, succinic, glutaric, and maleic acids) and/or bases (e.g., amines). Sulfuric acid (H2SO4), by contrast, has extremely low volatility and can be treated as entirely in the condensed phase for most applications. Metal cations, including those found in dust and sea salt, are also essentially nonvolatile. The abundance of these various constituents is a function of emission source and atmospheric processing and ultimately dictates the pH of fine particles (Figs. 1, 2).
Although aerosol and cloud acidity are distinct in many ways, aerosol forms in part from cloud evaporation, and so aerosol composition and acidity may be directly affected by cloud chemistry. Similarly, cloud droplets and ice crystals nucleate on preexisting particles, and therefore much of the material that modulates cloud acidity originates from the precursor aerosol. Cloud droplets can collide with surfaces resulting in occult deposition (Dollard et al., 1983) or precipitation in the form of rain. With these connections in mind, both aerosol and cloud acidity are important to human health, ecosystem health and productivity, climate, and environmental management.
The acidity of atmospheric deposition for dry, wet, and occult (wind-driven cloud water) pathways is directly affected by aerosol and cloud pH (Fig. 1). Thus, programs designed to reduce acid rain (e.g., the Acid Rain Program under Title IV of the 1990 Clean Air Act Amendments in the US) have had implications for particle and cloud droplet acidity. In terrestrial ecosystems, direct effects of acid deposition to foliage include leaching of cations, altered stomatal function, and changes in wax structure (Cape, 1993). Acid deposition can exacerbate soil acidification (Binkley and Richter, 1987), resulting in loss of soil base cations, leaching of nitrate, and mobilization of aluminum, affecting terrestrial ecosystem health and the quality of water delivered to streams and lakes (Driscoll et al., 2007). Apart from reactive nitrogen, atmospheric deposition is also a significant source of limiting and trace nutrients such as phosphorus (P), iron (Fe), and copper (Cu), especially in the remote oceans (Mahowald et al., 2008; Myriokefalitakis et al., 2018). While mineral dust is a major source of these nutrients, combustion sources also emit iron, copper and other trace metals (Reff et al., 2009; Ito et al., 2019). Acid processing of aerosol prior to deposition may greatly enhance the solubility of all these compounds, increasing their bioavailability and ecosystem impacts (Meskhidze et al., 2003; Nenes et al., 2011; Kanakidou et al., 2018). For example, dust aerosols coated by acidic sulfate and nitrate show increased Fe solubility compared to fresh dust particles, particularly in the fine mode, the deposition of which may promote phytoplankton blooms in nutrient-limited regions of the oceans (Meskhidze et al., 2005). The same process occurs for P (e.g., Nenes et al., 2011; Stockdale et al., 2016); however, the extent to which particle pH may similarly increase the solubility and amount of organic forms of nitrogen and phosphorus, a potentially large source to ecosystems (Jickells et al., 2013), is not well known (Kanakidou et al., 2018). Deposition of trace nutrients from acid-promoted dissolution into regions of the ocean where the nutrients are not limiting to biological productivity may enhance productivity in nutrient-limited regions by means of long-range transport by ocean currents. Such a redistribution of nutrients can have important implications for the biogeochemistry of the ocean, the oxygenation state, and the carbon cycle (Ito et al., 2016).
Aerosol acidity is also a governing factor for atmospheric dry deposition of inorganic reactive nitrogen species, which is a key nutrient driving primary productivity in terrestrial and marine ecosystems. The hydrogen ion activity in aqueous aerosols affects the partitioning of total nitrate () and total ammonium () between the gas and aerosol phases. Given the much larger deposition velocity of gases compared to submicrometer aerosols, pH-mediated partitioning influences the effective deposition velocity and lifetime of TNO3, TNH4, and total inorganic N (TNO3+TNH4). Acidity therefore also affects the magnitude and spatial patterns of inorganic N deposition to terrestrial and aquatic ecosystems. Lower aerosol pH favors partitioning of TNO3 toward gaseous HNO3 rather than aerosol , thus shortening its lifetime (Weber et al., 2016). In contrast, TNH4 () partitions toward gaseous NH3 at higher pH. Conditions of aerosol pH that promote a short residence time and local dry deposition of TNO3 may conversely result in longer-range transport of TNH4 and a more spatially extensive pattern of deposition and influence from source regions. The presence of dust and sea salt can influence not only pH but the size distribution (Lee et al., 2008, 2004) and the resulting deposition velocity of nitrate aerosol due to higher deposition velocities of coarse-mode compared to fine-mode particles (Slinn, 1977). Variations in scavenging efficiency, dependent upon cloud pH, can also affect atmospheric lifetimes and spatial deposition patterns of TNH4. HNO3, due to its strong acidity and solubility, is essentially partitioned entirely to cloud droplets for typical cloud pH values (>2). NH3 also mostly partitions into cloud drops for pH values below 6, but an appreciable fraction can remain in the gas phase for higher pH values. Biases in pH in atmospheric models can therefore influence the amount, speciation, and location of N deposition, with implications for determining ecosystem-critical load exceedances for nutrients and acidity (Bobbink et al., 2010).
PM2.5 is associated with adverse human health effects, including premature mortality (Di et al., 2017; Lepeule et al., 2012; Pope et al., 2009; US EPA, 2019). Aerosol acidity is associated with health effects of air pollution through its influence on atmospheric processes that affect the amount and composition of PM2.5 (Fig. 1). The concentration of fine particulate matter (PM2.5) is directly modulated by pH through its effects on gas–particle partitioning, pH-dependent condensed-phase reactions, and other particle processes influenced by pH. For example, N2O5 heterogeneous hydrolysis significantly affects tropospheric chemistry (Dentener and Crutzen, 1993) and depends strongly on particle composition (Chang et al., 2011), including formation of organic coatings due to liquid–liquid phase separation influenced by acidity (see Sect. 6.3 for a discussion of phase separation in the context of acidity). The strong acidity property of aerosol (Koutrakis et al., 1988) has historically been associated with adverse health effects (Dockery et al., 1993, 1996; Thurston et al., 1994; Raizenne et al., 1996; Spengler et al., 1996; Gwynn et al., 2000; EPA, 2009). One reason for this could be that aerosol acidity influences solubilization and the concentrations of toxic forms of trace species, such as transition and heavy metals, that have been linked to negative health effects (Kelly and Fussell, 2012; Lippmann, 2014; Rohr and Wyzga, 2012; Chen and Lippmann, 2009; Frampton et al., 1999). Transition metal ions (TMIs), such as soluble Cu and Fe from acid dissolution, contribute significantly to the oxidative potential of particles (Fang et al., 2017; Pöschl and Shiraiwa, 2015), which has been linked to cardiorespiratory emergency department visits with a stronger association than PM2.5 mass (Abrams et al., 2017; Bates et al., 2015). Ye et al. (2018) report a strong association between soluble Fe, which is modulated by particle acidity and aerosol water content, and cardiovascular endpoints. The mechanistic link between acidity, TMI dissolution, and health outcomes recently proposed by Fang et al. (2017) may help explain why sulfate in the ambient atmosphere is associated with adverse health outcomes, in contrast to studies that show little role for sulfate in negative health endpoints (Schlesinger, 2007; Reiss et al., 2007).
Aerosol acidity can affect the gas–particle partitioning of semivolatile toxic organic pollutants and therefore their environmental fate and pathways for exposure (Vierke et al., 2013). Some per- and polyfluoroalkyl substances (PFASs), including perfluoroalkyl sulfonic acids (PFSAs) and perfluoroalkyl carboxylic acids (PFCAs), are strongly acidic and likely to be at least partially dissociated (ionized) under pH conditions typical of most atmospheric aerosols (Ahrens et al., 2012). Once in the particle phase, pollutants are vulnerable to hydrolysis, which shortens their lifetime in the environment but may lead to the formation of toxic degradation products (Tebes-Stevens et al., 2017). Aerosol acidity was also recently shown to enhance airborne nicotine levels and resulting thirdhand smoke exposure by promoting volatilization from surfaces (such as clothes) and allowing distribution throughout a building's indoor air (DeCarlo et al., 2018). Similar behavior may be possible for other alkaloids (Pankow, 2001). Furthermore, aerosol acidity may also affect particle toxicity on a per mass basis (increase or decrease) by influencing organic aerosol composition (Arashiro et al., 2016; Tuet et al., 2017). Many organic compounds that are toxic (e.g., nitrosamines) can also be formed in the aerosol phase under acidic conditions; at the same time, other potentially toxic compounds (e.g., organonitrates) may hydrolyze under strongly acidic conditions (Rindelaub et al., 2016a). Even for nontoxic organic aerosol facilitated by acidity, the enhanced (or conversely reduced) formation of inert organic mass in the particle promotes the partitioning (or evaporation) of toxic species, such as polycyclic aromatic hydrocarbons (PAHs) (Liang et al., 1997), from the gas phase to the particle phase and thereby alters the location of deposition in the respiratory airways. For a highly soluble organic species, uptake to the aerosol phase can also potentially extend its atmospheric lifetime by slowing deposition to vegetation and ground surfaces.
Since acidity impacts the mass and chemical composition of atmospheric aerosols, which scatter and absorb radiation and serve as cloud condensation nuclei (CCN), acidity can also affect climate. First, particle pH influences, and is related to, the water uptake properties (hygroscopicity) of particles, which in turn can modulate both visibility and the radiative balance throughout the atmosphere (the aerosol direct climate effect). Cloud pH has been linked to the amount and speciation of aerosol upon evaporation, with important radiative effects (Turnock et al., 2019). Changes in acidity can also affect the number of chromophores contained within aerosol (so-called brown carbon) and their efficiency in absorbing sunlight in the near-UV range (Hinrichs et al., 2016; Teich et al., 2017; Phillips et al., 2017). Acidity-induced changes in aerosol affect the ability of particles to act as CCN and contribute to the formation of droplets in warm and mixed-phase clouds. For example, insoluble particles, such as dust, facilitate the production of ice crystals in mixed-phase and cold clouds (Seinfeld and Pandis, 2016); acidification of these particles can modify the active sites that ice is formed upon and thereby affect the distribution of ice and liquid water throughout the atmosphere (Sullivan et al., 2010; Reitz et al., 2011). The distribution of droplets and ice also may in turn regulate the riming efficiency in mixed-phase clouds (Pruppacher and Klett, 2010) and distribution of clouds throughout the atmosphere. Changes in cloud distribution strongly modulate Earth's radiative balance and the hydrological cycle (IPCC, 2007).
Atmospheric acidity also plays an important role in new-particle formation, which is thought to contribute up to 50 % of the CCN concentrations in the atmosphere, thus acting as a climate regulator (Gordon et al., 2017). Sulfuric acid likely plays a critical role in the formation of stable clusters upon which new particles are formed (Weber et al., 1997, 1998), while bases such as amines and NH3 (Jen et al., 2016) can facilitate the stabilization and growth of such clusters. Uptake of organic acids through acid–base chemistry (Zhang et al., 2004; Hodshire et al., 2016) and acid-mediated secondary organic aerosol (SOA) formation (e.g., McNeill, 2015) impact the aerosol size distribution with implications for CCN concentrations, cloud droplet formation, and climate.
Understanding particle acidity can facilitate improved air quality management strategies and policy planning to mitigate the health and environmental effects of air pollution. Consideration of different policy options and the development of emission reduction strategies often relies on chemical transport model (CTM) simulations of future conditions. Such modeling depends on the capability of CTMs to adequately simulate responses to policy scenarios. The predictive capability of CTMs is closely linked to their ability to track particle acidity through the pathways shown in Fig. 1. Some studies have pursued the development of observation-based indicators for the sensitivity of pollutants to precursor emissions for use in CTM evaluation and air quality management (e.g., gas ratio, Sect. 3). However, the use of the sensitivity indicators has been limited because their robustness has not been well established. Recent work (Shah et al., 2018; Vasilakos et al., 2018) has begun to explore the influence of particle acidity on the simulated responsiveness of PM2.5 to emissions changes. Vasilakos et al. (2018) demonstrated that reliable predictions of particle pH in CTMs are key to modeling the response of PM2.5 components to precursor emission changes. Furthermore, pH biases may propagate to biases in nitrate partitioning, dissolved metal concentrations, inorganic and organic aerosol amount and composition, and aerosol size distributions and ultimately could affect predicted impacts of emissions on ecosystem productivity and public health.
This study reviews the current understanding of aerosol and cloud acidity in the atmosphere. The work is motivated by the central role of aerosol and cloud acidity in numerous complex atmospheric processes of importance to human health and welfare as well as the rapid growth in literature on aerosol acidity in recent years. Despite decades of research on these processes, relatively few observational constraints exist for model evaluation. This review aims to collect values of fine-aerosol and cloud pH as well as discuss the approaches used to determine them. We provide an overview of the range of pH acidity scales and methods of approximating pH as well as discuss their challenges and advantages (Sect. 2). In addition, we discuss proxies of pH (Sect. 3), insights from box modeling of particle pH and its approximations and proxies (Sect. 4), the role of chemistry in driving and being modulated by pH (Sect. 5), the role of particle size and composition (Sect. 6), observations of particle (Sect. 7.1) and cloud (Sect. 7.2) pH, and regional and global model representations of pH (Sect. 8).
Aerosol acidity is generally not directly measured, despite some recent progress (see Sect. 7.1.1–7.1.2). Instead, estimates are obtained from thermodynamic models that involve assumptions, which can vary according to the completeness of the atmospheric dataset being considered. The numerical value of pH also differs according to the concentration scale in use. Furthermore, pH has a number of different definitions – each devised for a particular application – and can only be measured accurately and with metrological traceability for dilute solutions. These facts are not always well understood. This section summarizes the formal definition of pH and operational definitions and approximations. Thermodynamic models used to calculate fine-particle pH are also discussed.
2.1 Definition of acidity in terms of the pH
The degree of acidity or basicity of a solution can be quantified based on the thermodynamic activity (the effective concentration, including nonideal behavior) of dissolved hydrogen ions (H+). In the most common form, this measure of acidity is reported as a dimensionless quantity known as the pH. The International Union of Pure and Applied Chemistry (IUPAC) defines pH as (Buck et al., 2002; IUPAC, 1997)
where denotes the activity of H+ in aqueous solution on a molality basis, is the molality of H+ (mol kg−1, i.e., moles of H+ ions per kg of solvent, typically pure water), and is its molal activity coefficient (see Table 1 for a summary of definitions of pH and Appendix A for notation). The quantity mol kg−1 is the standard state (unit) molality used to achieve a dimensionless quantity in the logarithm (Covington et al., 1985) (omitted for simplicity in future equations). For solid particles or ice clouds, and potentially for glassy particles, a single pH value is undefined due to either the lack of a liquid aqueous phase or the potential for long intraparticle mixing timescales. In Eq. (1), both and are molality-based with a reference state of infinite dilution in pure water ( as . In most calculations involving natural systems the solvent is pure water, and therefore the molality, mi (mol kg−1), of solute species i is given by , where ni is the number of moles of i in the aerosol or cloud water particles, nw the number of moles of water, and Mw the molar mass of water. For some applications involving solutions containing large fractions of organic material that are miscible with water, the definition of the “solvent” may be altered to include all nonionic (organic) species. This is largely for practical reasons and because some thermodynamic models of activities in solutions and liquid mixtures (e.g., Yan et al., 1999; Zuend et al., 2008) require it. The activity coefficients used in the calculation of pH must be consistent with both the definition of what constitutes the solvent and also the concentration scale used. Further explanation is given in the Supplement (Sect. S1).
a For 1:1 electrolytes, . The difference between and pH is related to the activity coefficient ratio, . b With explicit normalization, pH.
The IUPAC definition of pH (Eq. 1) is regarded as a notional definition, because it involves the activity coefficient of a single ion (Buck et al., 2002; Covington et al., 1985). These are inaccessible experimentally because electrolyte solutions (of any relevant amount of substance) always contain both cations and anions, in proportions yielding an overall electroneutral system. Only mean activity coefficients of neutral cation–anion combinations are measurable quantities, such as in the case of the 1:1 electrolyte HCl (e.g., Prausnitz et al., 1999; Robinson and Stokes, 2002). Several, but not all, thermodynamic activity coefficient models used in atmospheric science and geochemistry provide a computation of single-ion activity coefficients within their mathematical framework (see later discussion of aerosol models, Sect. 2.6). However, these single-ion values are purely conventional in that they depend on assumptions inherent in the derivation of the model equations and, unlike mean activity coefficients, are not necessarily comparable between models.
2.2 Alternative pH concentration scales
Older definitions of pH by IUPAC, alongside Eq. (1), define the pH value on a molarity scale (pHc) (Covington et al., 1985):
The superscript (c) indicates the molarity basis for the activity () and activity coefficient (), distinct from the molality basis. The reference state is still infinite dilution in pure water ( as ), and the quantity mol dm−3 is the standard state molarity. The quantity denotes the molarity or molar concentration of H+ in an aqueous solution (i.e., mole of H+ per dm3 of aqueous solution; IUPAC, 1997). For dilute solutions, is practically equivalent to the molar amount of ion per dm3 of pure water. Covington et al. (1985) point out that for most applications involving dilute aqueous solutions, the pH and pHc values obtained from molality and molarity scales (for the same mixture) are of negligible numerical difference. The pH difference depends mainly on the density of water, and the difference in molal vs. molarity-based pH is approximately 0.001 pH units at 298.15 K, increasing to about 0.02 pH units at 393.15 K (with larger differences expected for concentrated aqueous electrolyte solutions and/or those with mixed solvents).
The mole fraction concentration scale is used by the Extended Aerosol Inorganics Model (E-AIM) of Clegg and co-authors (Clegg et al., 2001; Wexler and Clegg, 2002, and references therein). The pH on a mole fraction basis, pHx, is given by
where is the mole fraction of H+ in the solution, and and are the mole-fraction-based activity and the (rational) activity coefficient, respectively, both defined with respect to an infinite dilution reference state in pure water (superscript ∗ or (x)). The mole fractions of all species i, including water, are calculated as where the summation is calculated over all solution species j (ions, uncharged (e.g., organic) solutes, and water).
Conversions among pH values calculated using different concentration scales is necessary to compare model predictions and to report acidity on a consistent basis. Generally, formulae for the conversion of pH are derived based upon the equivalence of the chemical potentials of solution entities irrespective of concentration scale (see, for example, Robinson and Stokes, 2002). The conversions to pH from the equivalent values on the mole fraction and molarity scales are given below, and the derivations are given in the Supplement (Sect. S1):
where ρ0 (kg m−3) is the density of the reference solvent (pure water for the normal case, i.e., when activity coefficients on molality and molarity scale are defined with reference state of infinite dilution in pure water, regardless of a presence of organics in the solution). Because the density ρ0 depends weakly on temperature, the exact relation between pH and pHc is nonlinear. In the usual case of water as the reference solvent (ρ0 close to 1000 kg m−3), the logarithmic difference is small (typically <0.02 pH units), resulting in pHc≈pH (Jia et al., 2018).
2.3 Approximations of pH
Approximate values of pH, based upon the definition of pH (Eq. 1) but making simplifying assumptions, can be obtained in several ways. For example, the activity coefficient could be set to unity and pH computed based on only the free-H+ molality, symbol pHF:
The assumption of is appropriate only in highly dilute aqueous solutions, corresponding to ambient relative humidities close to 100 %.
Another approach is to use the mean molal ion activity coefficient of an H+–anion pair in place of ; i.e., , where X is a monovalent anion such as , , or Cl− (e.g., Wright, 2007). This approximation can be expected to capture the typical increase in with increasing H+ liquid phase concentration (decreasing ambient relative humidity, RH), although only semiquantitatively. The approximate pH determined in this way is labeled as :
The deviation of from pH is related to the ratio of the specified single-ion activity coefficients via . Consequently, the pH approximation by is very good for , which is the case in the highly dilute limit of aqueous electrolyte solutions. Further, it may also hold approximately towards higher electrolyte concentrations if both single-ion activity coefficients tend to deviate from 1.0 to a similar degree (which depends on aerosol composition).
An alternative to pHF would be to use the total H+ molality, which can be defined as the sum of dissolved H+ and molalities:
The use of this definition may be appropriate in contexts where the amount of free H+ is not of interest and/or the computation of bisulfate dissociation (which will vary with RH, aerosol composition, and temperature) is impractical. The use of pHF and pHT as alternatives to pH, as well as the assumption that , is tested by the intercomparison of thermodynamic model predictions for fine particles in Sect. 3.
2.4 Acidity and the pH scale
Expressing the acidity of a solution in terms of pH leads to a scale that has two important characteristics: an increase in acidity is accompanied by a decrease in pH and vice versa; and it is a logarithmic scale, meaning that a decrease by 1 pH unit corresponds to a 10-fold increase in H+ activity. Hence, apparently modest changes in pH represent relatively large changes in acidity.
A pH of 7 represents a neutral aqueous solution with values less than 7 generally considered acidic and values larger than 7 basic in nature. The characterization of pH equal to 7 as neutral is based on the chemical equilibrium between H+ and OH− ions arising naturally in aqueous solutions. The autodissociation of water () is described by the temperature (T)-dependent equilibrium constant on molality basis, Kw(T). The value of pKw () is 14.95 at 0 ∘C and 13.99 at 25 ∘C for pressures encountered in the atmosphere (Bandura and Lvov, 2005), resulting in corresponding pH values of about and 7.475 and 6.995, respectively, for highly dilute aqueous systems. Both systems are neutral, although the pH values differ.
The pH scale is commonly considered to span values from 0 to 14, but larger and smaller values are also possible as the scale has no specific limits. Current large-scale models (Sect. 8) and observations (Sect. 7) indicate that cloud pH has a global mean somewhere between 4 and 6 and ranges from around 2 to above 7 (Fig. 2). The global distribution of fine-particle (nominally particles of 2.5 µm in diameter and below, PM2.5) pH is bimodal, with a population of particles having a mean pH of 1–3 and another population, influenced by dust, sea spray, and potentially biomass burning, having an average pH closer to 4–5. Fine-particle pH can be negative (Sect. 7.1), particularly when sulfate is a major component, and is rarely predicted to exceed 7.
2.5 Measuring pH and operational definition of pH
The small sizes and associated liquid volumes of single particles (which are in chemical equilibrium with vapors) prevent the application of standard pH measurement techniques to individual aerosol particles and cloud droplets. Instead, samples of larger volumes must be collected (e.g., a population of droplets in the case of cloud water, Sect. 7.2) or other methods employed, including measurements of aerosol- and gas-phase compositions and the application of thermodynamic models (Sect. 2.6) to compute pH values via Eq. (1). With enough sample volume, particularly in the case of cloud droplets which typically have low ionic strengths, traditional pH measurement techniques can be used. The operational definition of pH is based on the principle of determining the difference between the pH of a solution of interest and that of a reference (buffer) solution of known pH by measuring the difference in electromotive force, using an electrochemical cell (e.g., a combination electrode coupled to a pH meter). High-precision measurements of absolute pH values of the reference buffer solution used for calibration are made with a so-called primary method using electrochemical cells without transference (Harned cells; see Buck et al., 2002). The uncertainty associated with typical pH measurements, which use glass electrodes, is on the order of 0.014 for ionic strengths <0.1 mol kg−1 and is expected to increase towards higher ionic strength (Buck et al., 2002). Further details on pH measurement methods and their relationship to Eq. (1) are provided in the Supplement.
The measurement of aerosol pH is problematic because of the difficulty in collecting sufficient sample material without perturbing its acidity and also due to the mismatch between ionic strengths present in atmospheric fine particles (>1 mol kg−1 and sometimes exceeding 100 mol kg−1, Herrmann et al., 2015) and the molal ionic strength for which normal operational techniques are appropriate (no more than about 0.1 mol kg−1). Values of pH based upon primary measurement methods, which are used for instrument calibration, cannot be readily defined at high ionic strength. This is because assumptions regarding the activity coefficient of the Cl− ion (which is needed to establish the pH value of the buffer) are limited to very dilute solutions. In addition, the calibration of the pH electrodes requires the ionic strengths of the buffer and test solution (e.g., an aerosol sample) to be low and similar in magnitude. A pH electrode, calibrated for dilute conditions, will yield a measured pH that is systematically in error to an unknown degree if placed in a solution of higher ionic strength (e.g., Wiesner et al., 2006). Similar considerations apply to colorimetric methods (see Sect. 7.1): the equilibria involving the chemical species that provide the color response depend not solely on but on the thermodynamic activities of the sensing species themselves. These will vary with the chemical composition and concentration of the solution. Thus, colorimetric methods also require calibration that is relevant to the solution media they will be used to measure.
2.6 Thermodynamic models for pH calculation
Given the operational difficulties associated with measuring aerosol pH (Sect. 2.5), estimates of the degree of acidity of particles generally depend upon the use of thermodynamic models. In atmospheric science, a number of different thermodynamic models are used to predict equilibrium gas–particle partitioning, liquid-phase activity coefficients, solid–liquid and liquid–liquid equilibria, dynamic mass transfer of semivolatile species, aerosol liquid water content (ALWC), and pH. Most models can treat both metastable (supersaturated) solutions or stable states (where solids have formed). Here, some of the most widely used models are described, focusing on their general approach, special features, and relevant species in the context of pH calculations. Advantages and disadvantages of four common thermodynamic models are summarized in Table 2.
The thermodynamic modeling approach inherent in some models (e.g., ISORROPIA, MOSAIC, and EQUISOLV II) does not yield single-ion activity coefficients that allow for calculation of pH via Eq. (1). For example, ISORROPIA II and MOSAIC nominally output information for pHF, and studies published prior to this work using those models (see Sect. 7.1) were approximating acidity by reporting pHF. In this work (Sect. 4), model source codes were modified to use the mean molal activity coefficients for different cation–anion pairs (e.g., (H+, ) or (H+, Cl−)) in the estimation of pH using . Section 4 and observationally constrained pH estimates focus on equilibrium conditions, although MOSAIC is often used to dynamically calculate the transient H+ amount.
2.6.1 Extended Aerosol Inorganics Model (E-AIM)
The Extended Aerosol Inorganics Model (E-AIM) is a thermodynamic model to calculate gas–liquid–solid equilibrium in aqueous aerosol systems containing inorganic ions, water, and an arbitrary number of organic compounds with user-defined properties. It uses the Pitzer–Simonson–Clegg (PSC) equations (Pitzer and Simonson, 1986; Clegg et al., 1992, 1998) for the calculations of solvent and solute activity coefficients (single-ion values) on the mole fraction scale. There are four principal models that differ in terms of the species and temperature range considered (Wexler and Clegg, 2002, and references therein; Friese and Ebel, 2010). The models include some or all of the following ions and the solid salts and gases that can be formed from them: H+, , Na+, , , , Cl−, and Br−. The possible calculations include the properties of an aqueous solution of defined composition, as well as the equilibrium state of a gas and particle system at defined RH and temperature. In chemical systems containing inorganic ions, the aqueous-phase equilibria , and are solved as well as those between aerosol species , , (aq), and with the gases NH3, HNO3, and HCl. Analogous equilibria (i.e., acid dissociation, gas–liquid equilibrium) can also be solved for user-specified mono- and dicarboxylic acids, as well as mono- and diamines. The model can be used for both acidic and alkaline aerosols.
The activity coefficients, and contributions to the water activity, of uncharged (or undissociated forms of) organic solutes are calculated using the Universal Quasi-Chemical Functional group Activity Coefficients (UNIFAC) model (Fredenslund et al., 1975). Organic anions are assumed to have the same activity coefficient model interaction parameters as or (according to their charge), and amine cations are assigned the same parameters as .
The E-AIM model is based upon thermodynamic data for pure aqueous solutions and mixtures over a wide range of temperatures. This basis in measurements, and the calculation of ionic activities in terms of interactions between pairs and triplets of solute species, makes E-AIM generally the most accurate (inorganic) thermodynamic model used in atmospheric science. Nevertheless, it has some known weaknesses: predictions of rising equilibrium RH with concentration in some aqueous –––H2O aerosols at about 250 K and below (Model II); and similar errors in aqueous aerosols at low RH and containing high concentrations of and Cl− (Model IV). To address the latter case some restrictions have been placed on the types of calculations that can be carried out (see http://www.aim.env.uea.ac.uk/aim/model4/input4a.html, last access: 7 April 2020). Most relevant to aerosol pH is the fact that calculated molalities of free H+, , and in aqueous H2SO4 – and therefore in mixtures containing the three ions – deviate somewhat from measurements of the stoichiometric dissociation constant of obtained spectroscopically (Knopf et al., 2003; Myhre et al., 2003). Myhre et al. (2003) show that there is good agreement between modeled and measured degrees of dissociation of () at room temperature up to 30–40 wt % acid (equivalent to 75 % to 56 % equilibrium RH), within the relatively large scatter in the data. At 50 wt % acid, and above, the calculated values are too low, meaning that the molality of free H+ is also too low. These differences increase for H2SO4 concentrations above 35 wt % (5.5 mol kg−1) and temperatures below about 240 K (Knopf et al., 2003). These errors do not necessarily lead to errors in pH as the stoichiometric activity of H+ (used in determination of pH, Eq. 1) in aqueous solution is accurately reproduced as indicated by accurate predictions of equilibria with acid gases (HNO3 and HCl, Figs. 6 to 12 of Carslaw et al., 1995).
2.6.2 AIOMFAC-based equilibrium model
The Aerosol Inorganic–Organic Mixtures Functional groups Activity Coefficient (AIOMFAC) model is a thermodynamic activity coefficient model treating liquid mixtures containing water, inorganic ions, and organic compounds. The model combines a Pitzer-type aqueous ion interaction model with a modified UNIFAC model (Fredenslund et al., 1975; Hansen et al., 1991), which was originally designed for organic mixtures. As in UNIFAC, AIOMFAC applies a group-contribution approach to cover a wide variety of organic compounds by a relatively small set of organic functional groups (∼16 main groups). The AIOMFAC expressions, parameterization and validation based on experimental data, and known limitations are described in detail elsewhere (Zuend et al., 2011; Zuend et al., 2008).
AIOMFAC presently includes the following inorganic ions: H+, Li+, Na+, K+, , Mg2+, Ca2+, Cl−, Br−, , , and (I− forthcoming). Most of these ions can be present simultaneously in an aqueous solution; limitations exist for Li+ in the presence of bisulfate () ions due to a lack of experimental data required for determining associated model parameters. However, using a less-rigorous analogy approach, AIOMFAC can approximate those parameters so that all listed ions can be treated in solution. The bisulfate dissociation equilibrium is solved numerically using the temperature-dependent equilibrium constant parameterization by Knopf et al. (2003). Other inorganic electrolyte species are considered completely dissociated when in liquid solution – with deviations from that assumption accounted for implicitly by activity coefficients. In contrast to the E-AIM model, AIOMFAC does not solve the dissociation equilibrium (which is acceptable when the pH is at least 1 pH unit lower than the neutral value). The organic functional groups available in calculations for mixed organic–inorganic systems include carboxyl, hydroxyl, ketone, aldehyde, ether, ester, alkenyl, alkyl, hydroperoxide, peroxyacid, peroxide, and aromatic functional groups. However, only a subset of these groups is currently available when , Mg2+, or H+ are present; see https://aiomfac.lab.mcgill.ca/about.html (last access: 7 April 2020) (Fig. 4 on that website). A few species are available exclusively for a select set of organic or inorganic systems, e.g., an organonitrate group in nonelectrolyte systems (Zuend and Seinfeld, 2012) and the methanesulfonate ion in certain organic-free aqueous solutions ( with H+, Na+, ; Fossum et al., 2018).
An online version of AIOMFAC is available at https://aiomfac.lab.mcgill.ca (last access: 7 April 2020) (and http://www.aiomfac.caltech.edu, last access: 7 April 2020). Note that the online AIOMFAC model is simply an activity coefficient model and not a complete gas–liquid thermodynamic equilibrium model. A limitation of AIOMFAC is that the composition-dependent degree of dissociation of organic acids (via the carboxyl group) is not accounted for explicitly in the determination of acidity. As such, the pH calculations are only meaningful in the presence of some amount of inorganic H+. Due to the weak temperature dependence of activity coefficients, the model is applicable over a temperature range of about 298 ± 30 K, while most of the experimental training data were for temperatures ≥293 K. AIOMFAC variants with a more sophisticated temperature dependence have been parameterized for electrolyte-free aqueous organic systems (Ganbavale et al., 2015).
A unique feature of AIOMFAC is its ability to represent nonideal interactions between organic molecules and inorganic ions in liquid solutions up to high concentrations, a feature that is important for the prediction of liquid–liquid phase separation. Thermodynamic equilibrium models have been developed with AIOMFAC as their core module, including efficient numerical methods for the prediction of liquid–liquid equilibria (Zuend and Seinfeld, 2013) and the equilibrium gas–particle partitioning of water and semivolatile organic compounds (Zuend and Seinfeld, 2012; Zuend et al., 2010).
Recent work further extends the AIOMFAC-based gas–particle partitioning model by consideration of the gas–liquid equilibria of the following inorganic acids and bases: HNO3, HCl, HBr, and NH3, while H2SO4 is treated as nonvolatile (Ma and Zuend, 2020). This equilibrium model is referred to as AIOMFAC–GLE hereafter. For given input in the form of molar amounts per unit volume of air at given pressure and temperature, the AIOMFAC–GLE model predicts the compositions of co-existing phases (gas phase plus up to two liquid phases) and associated activity coefficients of all species in all (liquid) phases. This enables a straightforward calculation of phase-specific pH values using Eq. (1).
The Model for Simulating Aerosol Interactions and Chemistry (MOSAIC) is a sectional aerosol model that treats aerosol thermodynamics, size-resolved dynamic gas–particle partitioning, heterogeneous chemistry, and coagulation (Zaveri et al., 2008). It includes all major inorganic salts and electrolytes composed of H+, , Na+, Ca2+, , , , , Cl−, and . Ions such as K+ and Mg2+ are represented by equivalent amounts of Na+ while other unspecified inorganic species such as silica, other inert minerals, and trace metals found in soil dust aerosols are lumped together as “other inorganic mass” (OIN). MOSAIC also includes carbonaceous species such as black carbon, primary organics, and secondary organics. Although organic–inorganic interactions are not presently treated explicitly in MOSAIC, organics and OIN species can absorb water, which indirectly affects the overall particle pH. The gas-phase species that can partition to the particle phase include H2SO4, CH3SO3H (methanesulfonic acid), HNO3, HCl, NH3, and any number of secondary organics.
At a given time step, the thermodynamics submodule MESA (Multicomponent Equilibrium Solver for Aerosols; Zaveri et al., 2005a) first determines the equilibrium phase state in each size section as a function of particle-phase composition, particle size (accounting for the Kelvin effect), relative humidity, and temperature, with aerosol water content calculated using the Zdanovskii–Stokes–Robinson (ZSR) method (Stokes and Robinson, 1966; Zdanovskii, 1948). The dynamic gas–particle partitioning module ASTEM (Adaptive Step Time-split Euler Method) then calculates the driving forces for mass transfer of the gas-phase species over each bin and integrates the associated mass transfer differential equations for all size sections (Zaveri et al., 2008). The mean stoichiometric activity coefficients of electrolytes for the equilibrium phase state and mass transfer driving force calculations are estimated using the Multicomponent Taylor Expansion Method (MTEM; Zaveri et al., 2005b). Briefly, MTEM calculates the mean molal activity coefficient of an electrolyte in a multicomponent solution on the basis of its values in binary solution for all the electrolytes present in the mixture at the solution water activity (aw), assuming that aw is equal to the ambient RH. For self-consistency most of the MTEM and ZSR parameters are determined using the comprehensive PSC model at 298.15 K. The PSC model is the basis of E-AIM.
In partially or fully deliquesced aerosols, the hydrogen ion molality () plays a central role in both equilibrium phase state and mass transfer calculations. For computational efficiency, two solution domains are considered on the basis of the so-called molal sulfate ratio, XT:
In the sulfate-rich domain (i.e., XT<2), the partial dissociation of the bisulfate ion () and electroneutrality equations are simultaneously solved to determine , which is subsequently used to determine the equilibrium gas-phase concentrations of HNO3, HCl, and NH3 at the particle surface for computing their driving forces for mass transfer. In the sulfate-poor domain (i.e., XT≥2), is assumed to completely dissociate to , and the use of equilibrium to calculate the driving forces produces spurious oscillations in the mass transfer of HNO3, HCl, and NH3. This problem is solved by introducing the concept of dynamic , which is determined by simultaneously solving surface equilibrium equations together with the acid–base coupled condensation approximation. At a given time, the dynamic is thus a function of the gas–liquid equilibrium constants and mass transfer coefficients of HNO3, HCl, and NH3 along with their gas- and particle-phase concentrations. When the gases and particles reach a steady state, the dynamic in each size section is equal to the equilibrium . See Sect. 6 for a further discussion of the role of particle size and mass transfer on pH.
2.6.4 ISORROPIA II
ISORROPIA II (Fountoukis and Nenes, 2007; http://isorropia.epfl.ch, last access: 7 April 2020) is a computationally efficient code that treats the thermodynamics of inorganic K+–Ca2+–Mg2+–– Na+–––Cl−–H2O aerosol systems. NH3, HNO3, and HCl are considered present in the solution. The current version, version 2.3, of the code is used in this work (see code website for version history). The discrete adjoint of ISORROPIA, called ANISORROPIA, has also been developed (Capps et al., 2012) using a combination of automatic differentiation of ISORROPIA II and postconvergence treatments (to account for discontinuities in the information flow during solution) to compute the sensitivities of all output parameters of the code to their relevant inputs with analytical precision.
ISORROPIA II can compute the equilibrium composition for two types of inputs: (a) forward, closed-system problems, in which the temperature, relative humidity, and total concentrations (gas + aerosol) of aerosol precursors are known; and (b) reverse, open-system problems, in which the temperature, relative humidity, and the concentrations of aerosol , , Na+, Cl−, , Ca2+, K+, and Mg2+ are used as input.
To reduce the computational complexity and increase solver speed, ISORROPIA II uses a segmented solution approach, where depending on the relative amounts of each aerosol precursor, major and minor species are defined. The equilibria of the major species together with conservation of mass and electroneutrality provide the equilibrium composition. ISORROPIA II uses mean activity coefficients for the cation–anion pairs in solution. For this, the Kusik and Meissner (1978) model for specific ionic pairs is applied in combination with the Bromley (1973) mixing rule for activity coefficients in the multicomponent mixtures found in the aerosol. ALWC is computed as a function of RH, using the Zdanovskii–Stokes–Robinson relation (Stokes and Robinson, 1966; Zdanovskii, 1948), using a water activity database computed from the E-AIM thermodynamic model, and incorporating the effect of temperature. Although the mean activity coefficients of all major cation–anion pairs are considered, for certain species (e.g., OH−, and undissociated ammonia, nitric and hydrochloric acid NH3(aq), HNO3(aq), HCl(aq)) unity activity coefficients are assumed due to a lack of corresponding data. Also, the first dissociation of sulfuric acid in solution is always assumed to be complete.
2.6.5 EQUISOLV II
EQUISOLV II is a model for calculating gas–aerosol equilibrium in atmospheric systems that contain water vapor; gases including NH3, HNO3, and HCl; and soluble inorganic electrolytes distributed across multiple particle size bins (Jacobson, 1999). Equilibrium is solved using a mass flux iteration technique. The model contains the major inorganic ions H+, , Na+, K+, Mg2+, Ca2+, , , , Cl−, and (Jacobson, 1999) as well as some minor and trace constituents. The thermodynamic treatment is summarized in chap. 17 of Jacobson (2005b).
Mean activity coefficients of the cations and anions in single-electrolyte solutions are calculated using polynomials fit to available data and reference values at 25 ∘C, supplemented by similar fits to values of enthalpies and apparent molar heat capacities of the solutions. Together, using standard relationships, these enable mean activity coefficients to be calculated for different temperatures. Mean ionic activity coefficients in mixtures are estimated using the approach of Bromley (1973), based on values for the constituent pure aqueous solutions at the total ionic strength of the mixture. The equilibrium is calculated explicitly and is based on the same thermodynamic treatment as in E-AIM (Clegg and Brimblecombe, 1995). The approach of Kusik and Meissner (1978) is used to estimate the mean molal activity coefficients and in mixtures in order to obtain the equilibrium concentrations of H+, , and (see Sect. 4.2 of Jacobson et al., 1996). This approach will not yield the same values as the treatment of Clegg and Brimblecombe (1995); see Sect. 4.1.
The relationship between the water content of aqueous aerosols containing multiple electrolytes and RH is estimated with the Zdanovskii–Stokes–Robinson relation (Stokes and Robinson, 1966; Zdanovskii, 1948), using polynomials representing single-solute molalities as a function of water activity (equivalent to equilibrium RH), and incorporating the effect of temperature, based upon the same enthalpy and heat capacity data as for the solutions referred to above.
2.6.6 Other thermodynamic models
Many other thermodynamic models have been developed for the prediction of atmospheric aerosol hygroscopicity and related properties, including the Gibbs free energy minimization model, GFEMN (Ansari and Pandis, 1999), for inorganic aerosol systems; ADDEM (Topping et al., 2005a, b), which emphasizes consideration of droplet size (Kelvin effect); and UHAERO (Amundson et al., 2007, 2006), which allows for the computation of complex phase diagrams of both inorganic and organic systems. These models are based on the PSC model for activity coefficient and pH calculations, either directly or via polynomial expressions fitted to that model (and are thus related to E-AIM). The models SCAPE and SCAPE 2 (with NVCs), for inorganic aerosol thermodynamics (Kim and Seinfeld, 1995; Kim et al., 1993a, b), implement several activity coefficient methods, including Bromley's method (Bromley, 1973), the Kusik and Meissner method (Kusik and Meissner, 1978), and a Pitzer model. The Equilibrium Simplified Aerosol Model (EQSAM) (Metzger et al., 2002, 2006) computes gas–liquid–solid partitioning for aqueous inorganic aerosol systems, including crustal cations and iron (II, III) species. The numerical complexity of thermodynamic equilibrium models has also led to work focused on the design of computational solvers for high efficiency; for example, HETV (Makar et al., 2003) is a vectorized solver for the SO4–NO3–NH4 system based on the ISORROPIA algorithms. All these thermodynamic models provide a theoretical basis and mechanism to link cations and anions in aqueous solution to pH or one of its approximations.
pH has been referred to as a master variable as a result of its fundamental role in the condensed-phase environment (Stumm and Morgan, 1996.) including the processes highlighted in the introduction (Sect. 1) and later in Sect. 5. This role suggests that any study interested in understanding processes influenced by particle acidity (e.g., gas–particle partitioning, acid-catalyzed reactions, metal dissolution) should examine pH. Due to the lack of direct measurements of aerosol pH (see Sects. 2.5, 7.1) as well as requirements for data used to calculate pH (Table 2), multiple methods have been employed in the literature as surrogates or proxies for particle acidity. In some cases, proxies are used to infer a pH and whether particles are acidic or basic. In other cases, concepts related to pH, such as PM sensitivity to ammonia vs. oxidized nitrogen, are interpreted via molar ratios of species, but pH itself is not discussed as a central concept. Since the underlying processes affecting the endpoint of interest (e.g., gas–particle partitioning of semivolatile species that contribute to PM mass) are often dictated by pH, pH is implicitly contained in such an analysis. However, since proxies have only an indirect connection to the system's acidity, interpretation of results without information on pH can be challenging; incomplete; and, in the worst case, incorrect.
In this section, the most common aerosol pH proxies are defined and historical context for their development and use provided. Proxies are indirectly related to pH and thus differ from the approximations highlighted in Sect. 2.3. Section 4 expands upon the information presented here and in Sect. 2 by evaluating the effectiveness of each proxy using box model predictions of acidity based on ambient data.
3.1 Proxies based on electroneutrality
Two of the most commonly used proxy methods for aerosol pH, the cation ∕ anion equivalent ratio (also called the cation ∕ anion equivalence ratio or molar ratio, Hennigan et al., 2015) and the charge balance (also called the ion balance and sometimes strong acidity, Table 3), are based upon the principle of solution electroneutrality. In both approaches, H+ is assumed to balance the excess of anions. In the case of a molar ratio, the amount of H+ is assumed to scale inversely with the level of the cations relative to anions.
Application of the molar equivalent ratio to infer acidity began with studies comparing measured strong acidity to in aerosol samples (Lee et al., 1993, 1999; Liu et al., 1996), because direct measurements of strong acidity (e.g., via extraction and measurement by pH probe such as EPA Method IO-4.1) have biases associated with sample collection and challenges with data interpretation. The concept of the cation ∕ anion equivalent ratio was first applied to and measurements to infer the chemical forms (e.g., NH4HSO4 vs. (NH4)2SO4) of these abundant ions (Junge, 1963; Wall et al., 1988; Moyers et al., 1977; Lewis and Macias, 1980; Macias et al., 1981).
Electroneutrality and the cation ∕ anion equivalent ratio require consideration of all ionic species present in solution in a given particle. However, practical measurement limitations and assumptions have led to variations of the cation ∕ anion equivalent used throughout the years. One such assumption is that H+ accounts for the charge deficit between the water-soluble species present in particles that can be readily measured with an ion chromatograph. This typically includes five cation (, Na+, Ca2+, Mg2+, and K+) and three anion (Cl−, , and ) species (e.g., Quinn et al., 2006; Sun et al., 1998), though it occasionally includes a limited group of organic anions (Kerminen et al., 2001). A similar definition has also been applied to the nonrefractory inorganic species measured with an Aerodyne Aerosol Mass Spectrometer (, , , and partial Cl−) (Zhang et al., 2005; Quinn et al., 2006). If the aerosol is near neutral (pH ≈7) or acidity is dictated by components other than the inorganic ions in the balance (e.g., organic acids), then charge balance will not provide meaningful information (Trebs et al., 2005; Lawrence and Koutrakis, 1996). Further, the carbonate system (CO2(aq)–H2CO3––) must be included in the ion balance when the pH is near neutral or higher (Winkler, 1986).
The molar equivalent ratio is frequently simplified to consider only , , and (Pathak et al., 2009). The justification for this assumption is that these species represent the dominant fraction of inorganic ions, thereby controlling acidity in environments with low levels of crustal species and minor marine influence (Zhang et al., 2005). Nonvolatile cations have the potential to drive large-scale patterns in pHF (see Fig. 2 as well as Sect. 8), thus making proxies without nonvolatile cations potentially invalid over large parts of the globe. Several variations of the molar equivalent ratio using these three species have been developed. The degree of sulfate neutralization (DSN), introduced by Pinder et al. (2008a), is defined as
where each term represents the molar concentration of each species in the particle phase. Measurements of sulfate do not usually distinguish between bisulfate and sulfate (Solomon et al., 2014), so total sulfate, [TSO4], is used . The bisulfate anion is often more abundant than the sulfate ion in fine particles; however, TSO4 is often conceptualized has having an effective charge of negative 2. Similar to DSN, the degree of neutralization (DON, Adams et al., 1999) has been suggested, defined as
Other names have been applied to the DON, including the neutralization ratio (Lawal et al., 2018). The DON represents the ammonium associated with sulfate + nitrate, while DSN represents the ammonium associated only with sulfate. In principle, this suggests that they account for different aspects of particle acidity (Pinder et al., 2008a); however, DSN and DON were highly correlated in California (r2=0.961) and the southeastern US (r2=0.978) (this work, not shown), two locations with very different levels, suggesting that they represent the same physical parameter. The importance of this correlation as an indicator of pH, and its general validity, remains to be studied.
Finally, the simplest form of the cation ∕ anion molar equivalent ratio considers particle acidity based solely on the ratio. This simplification further requires that is relatively low (Xue et al., 2011). Acidic conditions are inferred when the measured molar ratio is less than two (Turpin et al., 1997), as this is assumed to indicate when mildly acidic ammonium sulfate particles begin containing progressively larger amounts of acidic ammonium bisulfate. Particle acidity and pH are assumed to scale with , with decreasing ratios corresponding to decreasing pH (Zhang et al., 2007).
More recently, the total ammonium-to-sulfate ratio has been proposed as an indicator of pH (Murphy et al., 2017):
Thermodynamic predictions from E-AIM were interpreted using this ratio to show that pH and ammonia volatilization increases as TNH4:TSO4 varies from below 1 to above 2 (coinciding with formation of sulfate over bisulfate). While the TNH4:TSO4 proxy may not give a precise pH estimate, it can provide general information. For example, the ratio of NH3:SO2 emissions had been used to predict that aerosol pH may increase in the near future (Murphy et al., 2017) despite relatively constant levels in the recent past (Weber et al., 2016).
In the case of charge balance, the amount of H+ is determined from the total cation ∕ anion deficit; for this reason, it is expressed as hydrogen ion concentration in air, i.e., total molar H+ amount per unit volume of air containing aerosol particles and/or cloud droplets, (nmol m−3 air or similar). is related to pH; however, the two are not expected to correlate since the former is an extensive property while the latter is an intensive property of an aerosol distribution. For example, a highly acidic (pH <1) particle with a low mass may have a lower than a much larger, moderately acidic (pH >4) particle. Further, lacks direct modulation by particulate volume (liquid water, the solvent for H+) and activity coefficients. Diurnal variations in RH have been shown to cause pHF variations on the order of 1 pH unit in the eastern US (Guo et al., 2015; Battaglia et al., 2017; see Sect. 7.1). Like the cation ∕ anion equivalent ratio, the charge balance metric also assumes specific forms of dissociation state for multivalent ions (particularly for sulfate) and is strongly influenced by measurement uncertainty for each ionic species, especially when the aerosol is mildly acidic. These are all reasons why Guo et al. (2015) found only a weak correlation between and pHF (r2=0.36). Measured aerosol composition can also be used to create charge balance estimates of H+ in air. This method is also referred to as ion balance and sometimes strong acidity in the literature (e.g., Ito et al., 1998). When charge balance is performed on observations, it usually means a summation of all charge-equivalent anions and cations in the particle. Excess molar charge equivalents of anions compared to cations are assigned to :
Thermodynamic equilibrium models (Sect. 2.6) use charge balance (reflecting the requirement for solution electroneutrality) as an equation or constraint together with all other considerations of species equilibria across the phases present to obtain a unique solution. Some thermodynamic equilibrium models also use the cation ∕ anion equivalent ratio to enhance computational efficiency by identifying major ionic species and compositional domains (e.g., Pilinis and Seinfeld, 1987; Kim et al., 1993b; Nenes et al., 1998; Fountoukis and Nenes, 2007). However, thermodynamic models do not use charge balance from input data as a proxy for pH. Thermodynamic models (either manually, or automatically) evaluate inputs, in terms of a charge balance, to ensure that the solution obtained is atmospherically relevant – as an excess of nonvolatile cations may imply a strongly alkaline solution that is not found in the atmosphere. This aspect is discussed in more detail in Sect. 4.
Operationally, from charge balance is subject to errors associated with measuring aerosol-phase composition which are likely to be large and affect interpretation of ambient conditions. These are the same challenges that arise in thermodynamic calculations based on particulate-only inputs where biases or uncertainty in the measured species can propagate to errors in acidity (Hennigan et al., 2015; Song et al., 2018). When is small in concentration or species contributing to the charge balance are incompletely characterized, the proxy may return a value of zero or negative (indicating a surplus of cations) – neither physically possible – due to limited precision and accuracy in the measurements. Using measured aerosol composition, Murphy et al. (2017) and Hennigan et al. (2015) typically found negative values (indicating no H+, theoretically impossible) of H+ from charge balance and an error range large enough to span both positive and negative estimates at almost all times. State-of-the-art measurements are not sufficiently precise to overcome this limitation (Murphy et al., 2017). The problems associated with this proxy are highlighted in Sect. 4, where charge balance estimates near zero show no correlation with pH.
In the 1980s–1990s, experimental methods were developed to estimate the apparent net fine-particle (<2.5 µm) strong acidity (Koutrakis et al., 1988, 1992; Purdue, 1993). These methods, synthesized in a workshop report (EPA, 1999; Purdue, 1993), resulted in an officially documented method for estimating from measurements. EPA Method IO-4.1 used filter extracts in combination with measurements from a commercially available pH probe (titration methods are another option) to calculate an estimate of or H+ as equivalent mass of sulfuric acid. The method relies on efficient particle collection with minimal filter artifacts and low amounts of nitrate compared to sulfate (EPA, 1999). For example, ammonia could displace H+ and neutralize acidic particles during collection without an efficient denuder (Koutrakis et al., 1988). Extraction and dilution of ambient samples modify their chemical environment such that the conditions during measurement are different from those in the ambient atmosphere, potentially affecting gas–particle partitioning of total ammonium and dissociation of weak acids including bisulfate (Purdue, 1993). Variations of this method were developed to limit the extent of dilution by measuring the pH of droplets on the surface of a hydrophobic filter using microelectrodes (Winkler, 1986; Keene et al., 2004). However, the extent of dilution is still enough to shift the sulfate–bisulfate equilibrium outside of conditions present in many atmospheric particles. The use of a strong acidity proxy in many past health studies complicates their interpretation regarding the role of acidity since is only a proxy for pH.
Proxies for acidity have been used in a variety of applications. In the past, proxies were specifically applied in the context of acid-catalyzed SOA. Evidence for this phenomenon was sought in ambient data based upon landmark studies that demonstrated an important role of acid-catalyzed reactions in forming SOA in laboratory systems (Jang et al., 2002; Paulot et al., 2009; Surratt et al., 2010). However, due to a lack of direct particle acidity measurements (see Sect. 7.1 for details and discussion), researchers used different acidity proxies to characterize the impacts on SOA formation in the atmosphere. The molar ratio was used in several studies (Zhang et al., 2007; Peltier et al., 2007; Tanner et al., 2009) to infer that more acidic conditions did not enhance SOA concentrations. Froyd et al. (2010) used airborne measurements of the ratio to classify acidic and neutral particle regimes, and they inferred a causal effect of acidity on isoprene organosulfate formation at low NOx in the eastern US. Strong associations between SOA concentrations or SOA marker compounds and H+ derived from the charge balance were inferred in multiple locations (Pathak et al., 2011; Feng et al., 2012; Budisulistiorini et al., 2013; Nguyen et al., 2014). Several other studies investigated the relationship between particle acidity and atmospheric SOA using different predicted or derived measures of acidity. estimates based on operational extraction methods were used extensively in the literature to link SOA formation to acidity (Surratt et al., 2007; Offenberg et al., 2009; Zhang et al., 2012). In Beijing, Guo et al. (2012b) found evidence of acid-catalyzed SOA based upon correlations between secondary organic carbon (SOC) concentrations and H+ concentrations (nmol m−3) from ISORROPIA, run without gaseous inputs. Li et al. (2013) also observed correlations between SOA markers and acidity in China using pH predictions from E-AIM with aerosol inputs only. No evidence for acid-catalyzed SOA formation was found in a separate study in Pittsburgh, PA, that analyzed correlations between modeled H+ and measured SOA concentrations (Takahama et al., 2006). Takahama et al. (2006) used gas and particle phase inputs for predictions with the GFEMN model and also observed no correlations between pHc (with set to unity) and SOA. The studies employing proxies likely suffered from problems with the proxies; themselves (as discussed above); and confounding factors such as correlations between organic aerosol and sulfate, a major source of acidity, that often occur in regional pollution (Sun et al., 2011; Nguyen et al., 2015). These seemingly contradictory results were resolved once pHF was used, and the conclusions reached in these prior studies have been revisited based upon detailed understanding of the underlying chemical mechanisms and additional insight suggesting that the aerosol acidity is frequently not a limiting factor in catalyzing SOA formation (Surratt et al., 2010; Xu et al., 2015; Weber et al., 2016). Acid-catalyzed isoprene SOA has now been implemented in a wide variety of box model and chemical transport model applications that now rely exclusively on thermodynamic models for acidity estimates (Pye et al., 2013; Marais et al., 2016; Riedel et al., 2016; Budisulistiorini et al., 2017). So, while proxies can provide some information on the PM system, they should not be overinterpreted as a measure of pH.
3.2 Gas ratio
The gas ratio (GR) was defined by Ansari and Pandis (1998) to address the realization that inorganic PM concentrations do not always respond linearly to changes in sulfate concentrations (a common assumption at the time) and sought to develop a parameter that could be used for policy requiring only measurement network data. The underlying reason for this nonlinear response is that gas–particle partitioning of ammonium and nitrate is sensitive to pH. The gas ratio is defined in molar units as
and uses total ammonia () and total nitrate (). The numerator of the GR is sometimes referred to as free ammonia, because it is the amount of TNH3 that would be available to form NH4NO3 under the simplistic assumption that appreciable NH4NO3 does not form when the molar ratio of TNH4 to TSO4 is less than two (i.e., the stoichiometric ratio of (NH4)2SO4). The concept of free ammonia is discussed in greater detail below (Sect. 4.2.3). The GR has not been used explicitly as a proxy for aerosol pH, but it has been used extensively to define aerosol and composition regimes that relate to acidity.
Ansari and Pandis (1998) characterized inorganic PM response for changes in TNH4, TNO3, and TSO4 as functions of the GR, temperature, RH, and system concentrations. Their analysis determined critical values of the GR that defined boundaries of the PM response regimes. As West et al. (1999) showed, the GR still requires complementary thermodynamic modeling to robustly explore the PM response for large sulfate reductions. Other applications of the GR include calculation of the GR as a function of altitude (Adams et al., 1999); characterization of the sulfate–nitrate–ammonia–water aerosol system in the context of natural and transboundary pollution over the US (Park et al., 2004); and exploration of the sensitivity of aerosol nitrate to changes in temperature, RH, TNH4, TNO3, and sulfate for Pittsburgh (Takahama et al., 2004). In addition, Blanchard and Hidy (2003) considered the GR in a study of the response of nitrate to changes in TNH4, TNO3, and sulfate in the southeastern US. A relationship was demonstrated between the GR and an excess-NH3 indicator that resembles free ammonia but accounts for chloride and nonvolatile cations. Pun and Seigneur (2001) used box model simulations to demonstrate that nitrate concentrations in California's San Joaquin Valley would be sensitive to HNO3 levels but not NH3.
Pinder et al. (2008a) investigated the response of PM to emissions of NOx, SO2, and NH3 and demonstrated with AIM thermodynamic modeling that NH4NO3 can form at low temperature even when the GR is less than zero, in contrast to previous assumptions. To address this limitation, they developed an adjusted GR (adjGR) that modified the calculation of free ammonia:
where DSN is the degree of sulfate neutralization. Using a chemical transport model, Pinder et al. (2008a) demonstrated that the response of nitrate concentrations to changes in SO2 and NH3 emissions could be reasonably represented as a function of the adjGR and GR, but the adjGR provided a better fit for cases where DSN differs significantly from a value of two. In a separate study, Pinder et al. (2008b) found a strong relationship between the adjGR and the sensitivity of inorganic PM concentrations to NH3 levels at sites in the eastern US.
Additional metrics similar to GR have been defined. Wang et al. (2011) considered the GR and adjGR in a study of the sensitivity of inorganic aerosols to NH3 in mainland eastern China. They also defined a new indicator, the flex ratio (FR), calculated based on predictions of a statistical response-surface model developed from about 100 CTM simulations probing the sensitivity of PM to NH3 and NOx emissions (See Xing et al., 2018, for a precise definition). Nitrate concentrations are more sensitive to NH3 than NOx emissions for FR >1, and nitrate concentrations are more sensitive to NOx than NH3 emissions for FR <1. The FR provides a relatively precise estimate of the transition point between NH3-rich and NH3-poor conditions for existing NOx emissions levels. However, use of the FR remains limited due to its dependence on the availability of response-surface model predictions, which are currently limited to regions in Asia (e.g., Xing et al., 2011; Zhao et al., 2015). Wang et al. (2011) reported that the nitrate response regimes indicated by the GR and FR were qualitatively consistent in their study.
The studies described above, and other studies (e.g., Campbell et al., 2015; Dennis et al., 2008; Lee et al., 2006; San Martini et al., 2005; Zhang et al., 2009), have used the GR and adjGR to understand the response of the sulfate–nitrate–ammonium–water aerosol system to changes in precursor concentrations and emissions. The GR provides a reasonable indication of the sensitivity of inorganic PM to changes in TNH4, TNO3, and sulfate in many cases. However, the GR and similar metrics do not consider the role of nonvolatile cations, and universally applicable ranges of the GR for demarcating response zones are difficult to define due to the dependence on other factors (temperature, RH, and system concentrations). The GR has not been used explicitly as a proxy for particle acidity, but the response of nitrate to precursor concentrations can be represented as a function of the GR using S-shaped curves (Pinder et al., 2008a) that resemble the sigmoid curves reported for gas–particle partitioning of TNO3 as a function of pH (Guo et al., 2016). Therefore, some relation is expected between these indicators and particle acidity, which is shown in Sect. 4.2.3. While the above studies applied different proxies, recent work demonstrates the direct role of aerosol pH in modulating the sulfate–nitrate–ammonium–water aerosol system. Vasilakos et al. (2018) demonstrate that nitrate partitioning in response to changing SO2 emissions also depends on NVCs, which must be properly accounted for to accurately model pH.
3.3 Semivolatile species partitioning
Aerosol pH affects the gas–particle partitioning of semivolatile acidic and basic compounds in the atmosphere, including inorganic (HNO3, NH3, and HCl) and organic (amines, formic, acetic, and oxalic acid) species. The underlying reason why pH affects partitioning is that the protonated and deprotonated forms of the species vary considerably in their volatility (Keene et al., 1998; Meskhidze et al., 2003; Guo et al., 2017b). Based on this insight, estimates of aerosol pH can be derived from simultaneous measurements of the abundance of a compound in the gas and condensed phases, assuming that the species in question are in thermodynamic equilibrium. For example, HNO3 partitioning is determined by
Reactions (R1) and (R2) are characterized by Henry's law constant (KH) and the acid dissociation constant (Ka), respectively. These equilibrium expressions can be combined (see also the derivations provided in the supporting information of Guo et al., 2017b, and Nah et al., 2018) and rearranged to yield
where is the partial pressure of nitric acid, is the nitrate activity in deliquesced aerosols, and is the H+ activity in the aqueous aerosols. pH can be expressed as the fraction of total nitrate in the particle (]∕[TNO3] by moles), the gas constant (R), temperature, equilibrium constants, and molality-based activity coefficients for species i (γi):
An analogous version of Eq. (17) could be applied to any monovalent acid–anion pair (e.g., hydrochloric acid–chloride partitioning). pH based on ( by mole) is slightly different.
where Ka is the acid dissociation constant for :
pH from Eqs. (17) and (18) becomes uncertain when Fp is in the vicinity of one or zero, especially when considering the effects of observational uncertainty.
Current analytical techniques allow for the direct measurement of nitric acid while the aqueous aerosol nitrate concentration can be derived from the aerosol nitrate mass concentration (µg m−3, directly measured) by using the ALWC (measured or estimated). Conversion from aqueous concentrations to activity requires activity coefficients, which can be computed (e.g., Clegg et al., 1992), obtained from one of the aerosol thermodynamic equilibrium models, or approximated with a relevant ion pair (pH±) (Sect. 2). Most studies to date have simplified the above expressions by assuming activity coefficients of unity (molal basis), with aqueous concentrations replacing species activities in Eq. (16) above (Meskhidze et al., 2003; Keene et al., 2004) and the resulting pH (Eqs. 17–18) becoming pHF.
Gas–particle partitioning of TNH4, total chloride (TCl = HCl + Cl−), and TNO3 are all candidates for estimating pH. The approach was first discussed in relation to the pH of sea salt aerosols in the marine boundary layer (Keene et al., 1998). However, the phase partitioning behaviors of HCl and HNO3 were inconsistent, as measured implied a pH in the ∼1–2 range, but levels implied a much higher pH (Keene et al., 1998). These discrepancies were postulated to result from positive biases in the measurements, uncertainties in the thermodynamic constants, and kinetic limitations to mass transfer (deviation from equilibrium); however, the effects of mixing state and ability to predict liquid water con- tent were not discussed. The first quantitative estimates of aerosol pHc (molarity basis; see Eq. 2) via partitioning were done by Keene and Savoie (1998) and used partitioning to characterize sea salt particles mixed with anthropogenic pollution. Meskhidze et al. (2003) used measured partitioning to quantify aerosol pHF, with specific applications to Fe solubility. Keene et al. (2004) extended the analysis and compared the size-dependent aerosol pHc predicted by the phase partitioning of NH3, HCl, and HNO3 in marine air. They observed general agreement in the pH predictions based on HNO3 and HCl partitioning, while acidity based on NH3 partitioning was systematically lower by ∼1–2 pH units. Keene et al. (2004) assumed was unity in their calculations and noted this as a likely source of uncertainty. In a study a decade later, Young et al. (2013) compared the aerosol pHc (by size, with computed by E-AIM) predicted by NH3, HNO3, and HCl phase partitioning at a continental location near Denver, CO. In this study, aerosol pHc derived from NH3 and HNO3 partitioning generally agreed, while pHc predicted from HCl partitioning was systematically higher by ∼1–2 pH units than the other methods. The authors attributed these differences to order-of-magnitude uncertainties in the Henry constant of HCl (Sander, 2015). Similar problems with partitioning were observed in the northeastern US, potentially due to uncertainties in the thermodynamic properties of HCl or nonvolatile cation measurement artifacts (Haskins et al., 2018). Aerosol pH (pHc and pHx both evaluated) derived from NH3 partitioning agreed well with E-AIM and ISORROPIA predictions under highly polluted conditions in Mexico City (Hennigan et al., 2015). In this study, HNO3 and HCl data were not available to compare with the NH3 partitioning calculations, so an evaluation of differences, as was performed by Keene et al. (2004), was not possible.
The partitioning of semivolatile carboxylic acids should also provide insight into aerosol pH conditions (Keene et al., 2004). Nah et al. (2018) found that oxalic acid partitioning was consistent with its known thermodynamic properties and thus represented a reasonable proxy for aerosol pH in a study in the southeastern US. However, in the same study, the partitioning of formic and acetic acid implied aerosol pH levels that were ∼5–6 pH units higher than that predicted by ISORROPIA or other semivolatile species, including oxalic acid (Nah et al., 2018). The reasons for such dramatic differences are not known, but the formation of organic salts may be one explanation (Paciga et al., 2014; Hakkinen et al., 2014; Tao and Murphy, 2019a).
Efforts to reconcile some of the above differences using model simulations are challenged by large uncertainties in the emissions (Kelly et al., 2016) and secondary formation (Millet et al., 2015) of key species. Although few other comparisons of aerosol pH based upon direct measurements of semivolatile partitioning have been conducted, semivolatile species partitioning is used as a key evaluation of thermodynamic model predictions of pH. Guo et al. (2015) compared ISORROPIA predictions of ALWC and NH3 partitioning with direct measurements in the southeastern US during the Southern Oxidant and Aerosol Study (SOAS). ALWC is required for accurate calculations of (hence pH), while NH3 partitioning (for aqueous particles) is dependent upon pH. Guo et al. (2015) observed excellent model–measurement agreement for both ALWC and NH3 partitioning, suggesting that their pH predictions were similarly accurate. Comparisons of modeled and measured semivolatile species partitioning are now regularly used to check thermodynamic model predictions of aerosol pH (e.g., Guo et al., 2016, 2017b, 2018b; Murphy et al., 2017; Nah et al., 2018; Song et al., 2018). For example, predictions of partitioning were systematically biased at RH below 40 %, suggesting that pH predictions under such RH conditions are likely problematic (Guo et al., 2016).
Practical measurement limitations have precluded more extensive evaluations of direct pH predictions with partitioning predictions of pH. First, the method requires measurable concentrations of a compound in both gas and condensed phases. Conditions in which a species is partitioned almost entirely to one phase preclude the application of this method. For example, Keene et al. (2004) were unable to make quantitative estimates of aerosol pH based upon formic or acetic acid partitioning since the aerosol concentrations were frequently below method detection limits. In certain environments, HNO3 is partitioned almost entirely in the gas phase, limiting its use for aerosol pH determinations. This limitation also extends to the ability to test and validate the thermodynamic models, whose phase partitioning predictions are a key model check since direct pH measurements are not yet applied to ambient particles (Liu et al., 2017). Second, this approach assumes instantaneous equilibrium, which does not always hold (see Sect. 6 for a discussion on deviations from equilibrium). The partitioning method is susceptible to biases associated with sampling semivolatile components in either the gas or particle phases. Due to their semivolatile nature, measurements of these compounds can suffer positive (overestimation) or negative (underestimation) artifacts, and the challenges associated with measuring organic (Turpin et al., 2000; Eatough et al., 2003; Lipsky and Robinson, 2006) and inorganic (Ashbaugh and Eldred, 2004; Talbot et al., 1990; Pathak et al., 2004; von Bobrutzki et al., 2010) semivolatile compounds have been well documented. Despite major advances in analytical capabilities, such challenges persist (Dhawan and Biswas, 2019; Guo et al., 2016; Tao and Murphy, 2019a). Finally, the assumption regarding the phase state of the aqueous aerosol (i.e., whether it is on the efflorescent or the deliquescent branch of the water uptake curve, given hysteresis) has a profound impact on the amount of liquid water present in the aerosol, which in turn affects the ionic strength and ion speciation in solution (hence pH). Although studies have confirmed that the liquid water content can be in agreement with observations (Guo et al., 2015) and in combination with semivolatile partitioning measurements provide a well-constrained estimate for aerosol pH, the ALWC predictions central to the pH calculations are not routinely evaluated. While organics do not appreciably affect pH in particles consisting of a single aqueous phase (Battaglia Jr. et al., 2019), the presence of organic species could result in highly viscous (semisolid or glassy) particles where the system is not at equilibrium and pH has a heterogeneous distribution throughout the particle. All these factors eventually limit the precision and range of atmospheric conditions for which pH estimates based on semivolatile species partitioning can be used. The accuracy of partitioning as well as other proxies as estimates of pH is further discussed in Sect. 4 (specifically Sect. 4.2.3 and 4.3) based on box model calculations.
This section applies the concepts introduced in previous sections regarding the definition of pH (Sect. 2.1), approximations of pH (Sect. 2.3), and proxies of acidity (Sect. 3). Specifically, E-AIM, AIOMFAC–GLE, MOSAIC, ISORROPIA II, and EQUISOLV II are used to carry out an intercomparison of pH predictions, approximations, and/or proxies using idealized and ambient fine-particle compositions. Observations of gas–liquid equilibrium of semivolatile inorganic compounds were obtained from published studies from North America, Europe, and China representing what can be found in typical regional and global model studies.
4.1 Idealized scenarios
4.1.1 Description of systems
In this section, well-constrained acidity calculations were carried out by the models described in Sect. 2.6. The test cases involve the prediction of gas–liquid equilibrium of water and semivolatile inorganic compounds as well as pH for a range of equilibrium RH. Three aerosol test systems are compared: (1) an ammonium- and sulfate-rich system; (2) a NaCl-rich, sea-salt-like aerosol system; and (3) a nitrate- and ammonium-rich, but relatively sulfate-poor system. For each system, moderately acidic and highly acidic conditions were investigated, while covering seven RH levels: 99 %, 90 %, 80 %, 70 %, 60 %, 50 %, and 40 %. All calculations were for a temperature of 298 K. Molar input concentrations were chosen to represent realistic atmospheric conditions, for example using gas-phase ammonia concentrations of 1.2–25 ppbv typical for suburban to polluted air (Wang et al., 2015) and sulfate amounts resulting in ∼3–8 µg m−3 inorganic aerosol mass concentration in the highly acidic cases. The input concentrations and conditions for the systems are summarized in Table 4. These input concentrations describe initial (nonequilibrium) total (gas + liquid) molar amounts per unit volume of air – except for water, which is constrained by the given RH. The thermodynamic models equilibrate the different dissolved species and volatile inorganic gases, including solving for the equilibrium degree of bisulfate dissociation () in the liquid aerosol phase, the ammonia–ammonium equilibrium, and the aerosol water content. Mean molal activity coefficients for (H+, ) or (H+, Cl−) cation–anion pairs are used in sulfate-rich and sulfate-poor systems, respectively, to estimate pH using (Eq. 7). The calculated pH values for all systems are summarized in Tables S3–S5.
System 1: water + .
The first test system is an acidic aqueous ammonium + sulfate ∕ bisulfate system. Input concentrations of the electrolytes include (NH4)2SO4 (99.9 % by mass or 50 % by mass for moderately and highly acidic cases respectively) and H2SO4 with a separate gas-phase input of NH3 (mol m−3 air), all of which are then subject to change within a thermodynamic equilibrium calculation. No solid–liquid equilibria were considered. The highest pH values predicted are ∼4 for the slightly acidic case at 99 % RH, while the lowest pH values of ∼0.53 were predicted for the highly acidic case at 40 % RH.
System 2: water + .
The second system represents an acidified sea-salt-like aerosol solution, in which Mg2+ was substituted by charge-equivalent amounts of Na+. A highly acidic and a moderately acidic variant were created by specifying different amounts of sulfuric acid. The input for this system includes HCl, some of which will exist in the gas phase.
System 3: water + (NH4)2SO4+ .
The third system represents an acidic, nitrate-rich, and comparably sulfate-poor aerosol (XT>2 in Eq. 9). It involves the gas–liquid equilibration of the inorganic base NH3 and the acid HNO3, critical for establishing the equilibrium pH in the system. In the moderately acidic case, the pH values at 99 % RH are ∼2.5, while the pH values for the highly acidic case at 40 % RH were near 1.5.
4.1.2 Comparison of pH predictions and approximate measures of pH
Results for systems 1, 2, and 3 are shown in Fig. 3 panels (a), (b), and (c) for moderately acidic and (d), (e), and (f) for highly acidic scenarios. The pH values predicted by those models accounting for the single-ion activity coefficient of H+ (E-AIM and AIOMFAC–GLE, solid symbols in Fig. 3) differ only slightly from each other. For example, the E-AIM and AIOMFAC–GLE calculations for system 1 yield pH differences of 0.03 to 0.2 pH units for RH between 99 % and 80 %, while differences in magnitude of 0.21 to 0.35 pH units result for RH between 70 % and 40 %. Differences are expected to be smaller at high RH, where high water contents result in relatively high dilution and model–model differences in activity coefficients become smaller (see Sect. 2.5 for challenges at high ionic strength). However, this system illustrates that even at 99 % RH the H+ activity coefficients deviate from a value of one and are as small as 0.4. The pH predictions solely based on free H+ (pHF, Eq. 6) frequently deviate from pH by 1 unit for the idealized scenarios considered here (Fig. 4). Predictions based on total H+ (pHT, Eq. 8) can differ from pH by up to 2 units.
MOSAIC, EQUISOLV II, and ISORROPIA II use mean molal ion activities when computing the dissociation of bisulfate, the gas–liquid equilibrium of ammonia, and other equilibria (single-ion activity coefficients are not computed by these models). Therefore, pH predictions with such models require an approximation, for example the application of the mean molal ion activity approach of Eq. (7) for pH±. Although not a perfect approximation, pH± predictions can be very close to those carried out with the single-ion activity coefficient consideration. For example, for the moderately acidic case in system 1 (Fig. 3a), MOSAIC predictions differ from those by E-AIM by about 0.03 pH units at 99 % RH (0.07 pH units with respect to AIOMFAC–GLE), 0.3 pH units at 80 % RH, and 0.46 pH units at 40 % RH (0.75 pH units with respect to AIOMFAC–GLE). For system 1, the MOSAIC pH± value is generally lower than the pH from E-AIM and AIOMFAC–GLE. In the highly acidic system 1 case, the pH difference between MOSAIC and E-AIM is within 0.03–0.21 units, except for a 0.33 pH unit difference at 40 % RH. The ISORROPIA II model shows the largest variation in predicted pH over the 99 % to 40 % RH range, especially for the highly acidic case (Fig. 3d). For reasons of enhanced computational efficiency, ISORROPIA II uses lookup tables to determine the water content at a specified RH for a given aerosol system and is run with a higher tolerance level for numerical convergence than, for example, AIOMFAC–GLE. These efficiency adjustments may contribute to a notable difference in predicted water content and resulting pH±, particularly at 99 % RH, compared to the predictions with more rigorous equilibrium solvers used by the other models.
Generally, the observed differences in pH predicted by the thermodynamic models occur due to a combination of reasons. These include (1) differing predicted liquid water content at given equilibrium RH (water activity); (2) the predicted degree of bisulfate dissociation, which depends on the aqueous-phase composition and the values of the predicted activity coefficients (for H+, , and ) involved in the equilibrium; (3) the gas–liquid partitioning of NH3 (or other volatile components for systems 2 and 3); and (4) the use of single-ion vs. mean molal ion activity coefficients in the calculation or approximation of pH. Reasons (1)–(3) affect each other directly, such that any inherent difference among the model equations, for example the temperature and ionic strength dependence of water and ion activity coefficients, will lead to a different equilibrium solution for the aqueous-phase composition and pH. The interplay among composition-dependent activity coefficients and the gas–liquid or ion dissociation equilibria are nonlinear and may amplify or dampen effects on predicted pH in a complex manner. Therefore, given the type of test computations with gas–liquid equilibria considered here, differences among models on the order of 0.05–0.2 pH units (or even larger at very high ionic strengths resulting at moderate to low RH) are to be expected. Within this range, pinpointing which of the models is closest to the truth is not possible, but in general, pH from models that calculate single-ion activity coefficients (and hence ) using a rigorous numerical approach are to be preferred over those that assume a unity H+ activity coefficient or those that assume a mean activity coefficient. Figure 3 indicates that the disagreement between model predictions typically increases with decreasing water activity (RH) for both moderately and highly acidic conditions.
For system 2 (sea-salt-like), all models predict the highest acidities (lowest pH) at high RH, with the pH values increasing with decreasing RH for both the slightly and highly acidic calculation variants (Fig. 3b, e). This is because most of the HCl in the system is present in the gas phase, and this amount remains relatively constant over the whole RH range. Chloride ion activity in the aqueous phase rises as RH decreases and the aqueous solution becomes more concentrated. As a result, H+ activity decreases with decreasing RH to compensate and so maintain equilibrium with the roughly constant partial pressure of HCl(g). This rise in pH may be unrealistic compared to typical ambient conditions due to the high HCl and absence of ammonia in this test case. The pH predictions by E-AIM model III and AIOMFAC–GLE agree well (absolute differences of 0.01 to 0.06 pH units). The MOSAIC and ISORROPIA II predictions of pH in system 2 were carried out using the ions (H+, Cl−) for pH±. For the moderately acidic conditions, the MOSAIC- and ISORROPIA-derived pH± are in good agreement with E-AIM only at 99 % RH (0.02 unit difference), while larger deviations of 0.15 to 0.75 pH units occur for 90 % to 40 % RH. In this moderately acidic case, MOSAIC, ISORROPIA II, and EQUISOLV II tend to systematically overpredict the pH value towards lower RH relative to the other models. In the highly acidic case, the MOSAIC–E-AIM deviation is between 0.07 and 0.43 pH units at RH <99 %. Such deviations are linked to large variations in the molality-based H+ activity coefficients ranging from ∼0.72 at 99 % RH to >30 at 40 % RH (see AIOMFAC–GLE values in Table S4), which lead to larger errors when mean molal activity coefficients are used to obtain pH±. This important influence of the H+ activity coefficient or its approximation via γ±(H+, Cl−) is exemplified by comparison of the ISORROPIA II predictions with E-AIM and the other models. The very high activity coefficients of H+ and Cl− predicted by E-AIM, which get larger as RH decreases, result in only very low molalities of H+ left in the aqueous aerosol. ISORROPIA II yields a mean activity coefficient of (H+, Cl−) that is very low compared to that of the other models and varies little with RH, which means that the predicted HCl concentration in the aerosol is substantially higher. This results in the lower, and rather invariant, predicted pH± by ISORROPIA II for RH <80 %. This example further indicates that assuming activity coefficients of unity in the computation of pHF based on free-H+ molality (or for pHT) can lead to errors in this approximation of actual pH values in concentrated solutions (see also Sect. 4.2).
The pH predictions by E-AIM model III and AIOMFAC–GLE agree relatively well for system 3, which contains mainly ammonium nitrate (Fig. 3c, f), especially in the moderately acidic case. There, pH differences are 0.02 units at 99 % RH and about 0.10–0.12 units between 90 % and 40 % RH, with AIOMFAC–GLE predicting the slightly lower pH. In the highly acidic case, the differences are similarly low above 70 % RH, while they are ∼0.18 to 0.25 pH units between 70 % and 40 % RH. The deviations between the E-AIM pH and MOSAIC, ISORROPIA II, or EQUISOLV II pH± are clearly larger than those between AIOMFAC–GLE and E-AIM. Even at high RH (>80 %), the acidity estimates from ISORROPIA II and MOSAIC can differ from each other by almost 1 pH unit (Fig. 3f). Furthermore, the models using mean molal activity coefficients disagree from E-AIM and AIOMFAC–GLE at the highest RH where relatively good agreement is expected due to more dilute conditions. There are several reasons mentioned above that may be responsible for these deviations. The activity coefficient value (reason (4) above) contributes to the difference between MOSAIC/ISORROPIA II/EQUISOLV II and the E-AIM and AIOMFAC–GLE models, because the mean molal ion activity coefficient used as a substitute for in the first three of these models can either over- or underpredict the single-ion depending on the solution composition. The differences in pH predictions by ISORROPIA II compared to those by AIOMFAC–GLE and E-AIM at 99 % and 90 % RH (Fig. 3f) are mainly because ISORROPIA II yields free-H+ molalities () that are similar at the two RH levels, whereas for E-AIM they differ by a factor of 4 (higher RH, lower molality). This difference seems to be related to variation in the predicted equilibrium gas–aerosol partitioning of total H+: at 99 % RH the cumulative particle-phase mass concentrations of (∼ total particle-phase H+) per unit volume of air predicted by E-AIM and ISORROPIA II are similar, but at 90 % RH ISORROPIA II predicts a factor of 6 less total H+ than E-AIM. At similar ALWC, this yields a lower and higher pH than expected at 90 %. Elucidating detailed differences in acidity predictions between the thermodynamic models for nitrate-containing systems like system 3 should be considered in future work.
Figure 4 compares the different pH estimation options proposed in Sect. 2.3 for use by models that do not predict the single-ion activity coefficient of H+. All calculations (for the systems shown in Fig. 3 and discussed above) were carried out using AIOMFAC–GLE for consistency, and E-AIM is expected to yield similar results. The pH approximations based on total or free-H+ molality imply the assumption of an H+ activity coefficient of unity. The comparison in Fig. 4 shows that these two options tend to show larger deviations from the molality-based pH predicted by AIOMFAC–GLE compared to the use of single-ion activity coefficients. Both pHT and pHF approximate pH within about 0.5 pH units under highly dilute conditions with pH greater than about 3. However, pHT becomes a poorer approximation of pH when pH values decrease below 3, mainly due to the increasing concentrations of . In the case of the three systems compared here, pHF is overall a better estimate for pH than pHT, such that use of total H+ is not recommended for atmospheric aerosols. The suitability of pHF as an approximation may be influenced by the specific system being tested (e.g., RH condition, composition) and needs of the application.
Overall, the AIOMFAC–GLE model results suggest that pH± (with (H+, ) or (H+, Cl−) as the ions for the computation of used in Eq. 7) is better than pHF or pHT in approximating pH. Computation of the mean molal activity coefficient based on (2 H+, ) leads to a better pH± approximation only in the moderately acidic case of system 1 (Fig. 4a) at RH <90 %, while it is worse than using (H+, ) in the highly acidic case of system 1 (open symbols Fig. 4a). Therefore, the use of a 1:1 electrolyte for pH± is recommended. This mean molal activity coefficient approach is recommended when ISORROPIA II, EQUISOLV II, or MOSAIC are used as thermodynamic models for the calculation of aerosol properties.
4.2 Ambient scenarios
4.2.1 Description of datasets and calculations
Datasets were selected to cover a broad range of acidity, temperature, RH, and species present that drive aerosol pH (Table 5). In addition to the major species , , and , the dataset also contained variable concentrations of and the nonvolatile species Na+, Ca2+, K+, and Mg2+ (not shown in the table). A total of more than 7700 data points were available for evaluation from Tianjin, China; the California Nexus (CalNex) campaign; Cabauw, the Netherlands; the Wintertime Investigation of Transport, Emissions, and Reactivity (WINTER) campaign; and the SOAS campaign, with ∼7200 data points having relative humidities above 35 % and spanning a temperature range from 252 to 305 K (see also Nenes et al., 2020). Given that the MOSAIC box model required – in its current implementation – a manual setup of each input condition, a few data points were selected from the total available in each dataset to compare against the corresponding predictions from the other models. The points were selected to span the range of RH and sulfate amounts encountered in the datasets. Four data points per study location were selected, giving 20 total simulations from MOSAIC to compare against. The MOSAIC inputs are summarized in Supplement Table S9 with results shown in Fig. S6.
Before thermodynamic calculations are carried out with E-AIM, AIOMFAC–GLE, MOSAIC, and ISORROPIA II, each data point was evaluated to ensure that the resulting thermodynamic solution was atmospherically relevant – i.e., with an alkalinity that does not exceed that of carbonate aerosol (e.g., CaCO3). Specifically, the charge-equivalent amount of cations is not allowed to exceed the abundance of anions which would result in considerable amounts of hydroxyl ion. In the case of E-AIM and AIOMFAC–GLE, the composition data were preprocessed and evaluated before input, while MOSAIC and ISORROPIA II evaluate the data automatically and issue error messages or apply adjustments to the input. The input composition data for each model consist of total amounts of Na+, K+, Mg2+, Ca2+, TNH4, TCl, and TNO3, in moles per unit volume of air. The prefix T emphasizes the fact that the final three of the amounts are totals of , NH3(aq), and NH3(g); and HCl(g); and , HNO3(aq), and HNO3(g). The amount of H+ needed to achieve charge balance is calculated from
This equation differs from the charge balance proxy introduced in Sect. 3 since it considers the total (gas + particle) amounts of semivolatile acids and bases rather than exclusively the particle phase as in Eq. (13). If the value of Z is zero, then the system is charge balanced with all TNH4 present as (during a model calculation NH3 can still partition into the gas phase, but this will occur by dissociation of ). If the value of Z is greater than zero, there is an excess of cations, a Z amount of TNH4 is assumed to exist as NH3, and the ion in the system is reduced to [TNH4 – Z]. If the value of Z is less than zero, there is an excess of anions even when all TNH4 is present as . In this case, an amount of H+ equal to −Z is added to the system. For E-AIM and AIOMFAC, the calculation of Z and adjustments specified above yield the starting point for the calculation. The amounts of , NH3(aq), NH3(g), , , HCl(g), and HNO3(g) in the system at the specified RH and temperature are determined by solving the relevant equilibrium equations. In MOSAIC, the excess Cl− and anions are transferred to the gas phase as HCl and HNO3, in that order, while any excess in the particle phase is balanced by adding H+ to the system. The adjusted gas- and particle-phase concentrations are then used as the initial conditions for further dynamic gas–particle partitioning. In the case of ISORROPIA II, the aerosol is required to be more acidic than aqueous CaCO3 at given a RH, so Z should be less than or equal to zero.
The presence of nonvolatile cations is handled slightly differently by the models. When calcium is present in ISORROPIA II, the code first forms CaSO4 as a precipitate (Fountoukis and Nenes, 2007). If there is any remaining Ca and its mole equivalent exceeds those of , , and Cl− combined, an error message is noted and the code assumes that the excess Ca2+ is in the form of CaCO3 and the pH of dissolved CaCO3 is prescribed at the given RH (see Sect. 6.1 for a discussion of carbonate chemistry and pH). If all Ca precipitates out as CaSO4, then the ISORROPIA II code examines if the mole equivalents of Na+, K+, and Mg2+ exceed that of the , Cl−, and remaining combined. If that is the case, an error message is issued, and the excess cations are ignored. Otherwise, the code then uses the inputs of Na+, free Ca2+, free , etc. to calculate the pH, ALWC, and semivolatile partitioning of TNH4, TCl, and TNO3. A similar approach is taken in MOSAIC, which assumes that the maximum possible amount of CaSO4 precipitates out over the full RH range, and any excess Ca after forming Ca(NO3)2 and CaCl2 is assumed to be in the form of CaCO3. MOSAIC does not explicitly treat K+ and Mg2+, which are instead represented by equivalent moles of Na+. Both E-AIM and AIOMFAC also assume that the maximum possible amount of CaSO4 precipitates out and is not considered in the gas–particle partitioning calculations for RH <98 %. Furthermore, E-AIM does not consider Ca2+, K+, and Mg2+ in the calculations but instead uses a charge-equivalent amount of Na+. For AIOMFAC–GLE model input, the electroneutral set of ions is mapped to a set of representative electrolyte components. To facilitate intercomparison among the models over a wide range in RH, aside from the consideration of the precipitation of solid CaSO4, the models were run using the assumption of the aerosol phase being present as an aqueous electrolyte solution, potentially supersaturated with respect to certain crystalline salts (also referred to as metastable mode in ISORROPIA). Since this assumption becomes invalid at low RH, the statistical evaluation of model–model differences and pH approximations was restricted to the RH range above 35 %, while model calculations were carried out with the supersaturated solution assumption including data points at lower RH.
During the calculation of the equilibrium composition and corresponding aerosol pH by ISORROPIA II here, all nonvolatile cations are converted into their mole-equivalent sodium concentrations. Also, data where nonvolatile cation concentrations exceed what is required to neutralize the amount of anions (sulfate, nitrate, and chloride) present are not considered. All models were allowed to predict partitioning according to their equations and property databases; therefore differences in pH and activity coefficients are a convolution of all differences in the underlying thermodynamic treatment (equilibrium constants, numerical solver tolerance thresholds, calculated activity coefficients, and aerosol water content). A comprehensive accounting of the effects of these differences will be the focus of future work – and here we present only the differences in pH between models and their different implementations of pH approximations.
4.2.2 pH and its approximations
The pH values predicted by AIOMFAC–GLE (Fig. 5a) and E-AIM (Fig. 5b) for the combined datasets show both the wide range of pH calculated for each of the datasets and the variability in the results from the two models. E-AIM and AIOMFAC–GLE agree in their trends, but differences increase as RH decreases (as the aqueous aerosols become more concentrated). Differences between the models are usually within 0.5 pH units. The most acidic systems are SOAS (Centreville, AL) in the southeastern US (pH range: to 2) and WINTER for measurements aloft in the northeastern US (pH range to 2), which in part is related to the very low NH3 concentrations and lack of nonvolatile cations. The extremely high acidity branch of WINTER data corresponds to measurements carried out aloft, where temperatures as low as 252 K were encountered. The low humidities in that environment decrease aerosol water to very low levels (Guo et al., 2016). The CalNex dataset is characterized by intermediate pH values, ranging between 0 and 2.5, mostly driven by higher NH3 levels and presence of NVCs. The Tianjin and Cabauw datasets are characterized by the largest concentration of NH3 and NVCs and for this reason have the highest pH, reaching a value of 5.
In order to understand the uncertainty introduced by using pHF or pH± instead of model-predicted pH, model results are examined for each campaign separately. Figure 6 presents the differences between pH predictions and approximations for the Cabauw dataset. Calculations of pH with AIOMFAC–GLE (left column) using the various approximations (pHF, pH±) have notably different structure than that using E-AIM (right column). In both models, the difference between pH± and pH rarely exceed 0.5 pH units, especially for RH above 60 %; pHF is characterized by larger differences but still mostly within 1 pH unit – and it reflects the effect of the log10 () contribution which is largest at the lowest RH. These results are consistent with prior studies that assume that the activity coefficient of H+ is equal to unity for the purpose of pH estimation (but not for solving the thermodynamic equilibria) (Song at al., 2018).
Results in Fig. 6 suggest that using a H+–X− ion pair and applying an activity coefficient in the calculation of pH± gives less scatter and absolute bias across the dataset than using pHF within a given model framework (E-AIM or AIOMFAC–GLE). The ion pair that leads to the best pH± estimate varies between AIOMFAC–GLE and E-AIM, with H+–Cl− and H+– showing overall the most promise. The H+– pair tends to exhibit a large scatter and systematic bias in the case of E-AIM, while it shows the least scatter and bias among all ion pairs in the case of AIOMFAC–GLE. Repeating this exercise for all the other datasets (Supplement Figs. S2–S5) partly supports these observations – but the pattern and magnitude of the differences (approximate pH minus pH) vary according to the aerosol compositions characteristic of each dataset. For the WINTER data in particular (Fig. S5), biases much larger than 0.5 pH units can be seen at lower humidity (which is especially notable for E-AIM). These deviations can be attributed to the value of the activity coefficient of H+, which becomes very large for the ultrahigh ionic strengths characteristic of the WINTER aerosols at intermediate and low RH. The H+ activity coefficient, which exceeds 10 and can reach up to 100, tends to decrease the pH between 1 and 2 units beyond what is expected from pHF (Fig. S5b). The results from AIOMFAC–GLE and E-AIM in Fig. 13 and Supplement Figs. S2–S5 show that the calculated values of the pH approximations differ between the models in quite complex ways, largely reflecting the different treatments of the activity coefficients. These are reflected in both the value of and the secondary effects on liquid water uptake, ion dissociation, and semivolatile partitioning.
Both ISORROPIA II and MOSAIC nominally output pHF (and can be modified to output pH±); using approximations (pHF or pH±) in place of pH introduces uncertainty. ISORROPIA-predicted pH approximations as a function of relative humidity compared to AIOMFAC–GLE (left column) and E-AIM (right column, Fig. 7) show that the deviation between pHF and pH increases as the humidity decreases, with the largest deviations occurring for the extremely acidic aerosol dataset of WINTER. However, for most cases, relative humidities above 60 % are correlated with a deviation from pH that is less than a unit (smaller differences are seen for AIOMFAC–GLE than E-AIM). Comparisons of MOSAIC calculations against the predictions from ISORROPIA II for the 20 selected cases (Table S9) indicated the two models produce pH± (H+, ), pH± (H+, Cl−), and pHF metrics that are highly correlated (r2≥0.96) with minimal offset (regression slope within 0.11 pH units of 1:1 line) between the models (Fig. S6). Using the H+– ion pair to express pH± from ISORROPIA provides the closest agreement with pH if AIOMFAC–GLE is used as a reference.
The pH errors between ISORROPIA II and AIOMFAC–GLE/E-AIM for all the datasets combined are summarized in Table 6. Using pH± (H+, ) as a pH approximation shows the lowest RMSE and mean bias error in the case of AIOMFAC–GLE predictions, followed by pH± (H+, Cl−) as the next best approximation. However, when considering E-AIM, the evaluation of all datasets shows that pH± (H+, Cl−) and pH± (H+, ) are favored over pH± (H+, ), as pH± (H+, ) shows an RMSE of ∼1 for the WINTER data, which were characterized by the lowest pH values. The comparison between thermodynamic models for the performance of pH proxies includes a convolution of numerous errors in the cases of ISORROPIA II, MOSAIC, and EQUISOLV II; therefore, they cannot be used to determine a priori which choice of anion is best for use in pH± (H, X). Some of the pH± (H, X) variants also show a larger dependence on RH than others, with the largest deviations from pH typically found towards the problematic region of lower RH (<50 %); see Fig. 6. Based on the combined evaluations of pH approximations by E-AIM and AIOMFAC–GLE against their own pH predictions (no model–model bias incurred), pH± (H+, Cl−) has the best agreement for the wide pH range examined, although any of the pH± variants work sufficiently well, especially at RH >60 %.
1 The pH, as defined by Eq. (1), was calculated using both AIOMFAC–GLE and E-AIM. The comparisons are presented in terms of the root mean square error (RMSE) and mean bias (MB) as pH (approx.) – pH, all in pH units. Results were calculated using all of the SOAS, Cabauw, CalNex, WINTER, and Tianjin datasets (combined) described in Table 5 (n=7222 points), with RMSE and MB calculations limited to data points with RH >35 %. RMSE and MB are calculated as follows: and , where N denotes the number of data points within the evaluated dataset and where pHapprox,j and pHj are the pH approximation and reference values of data point j. 2 Calculations by (b) AIOMFAC–GLE and (c) E-AIM covering the same combined datasets as in (a).
4.2.3 Comparison of proxies to aerosol pH
Several studies have compared certain proxies of acidity (Sect. 3; see also Table 3) to thermodynamic model predictions of pHF (Guo et al., 2015, 2016; Hennigan et al., 2015; Lawal et al., 2018; Murphy et al., 2017; Winkler, 1986). Predictions of pHF using the semivolatile partitioning approach (Eq. 18, Fig. 8a–c) were evaluated in Mexico City (Hennigan et al., 2015), but more commonly, due to the lack of direct aerosol pHF measurements for comparison, semivolatile species partitioning is often used as a critical check of thermodynamic equilibrium model assumptions and predictive skill (Guo et al., 2016, 2017a, 2015; Nah et al., 2018). Connecting the neutrality-based or gas-ratio-type proxies to a numerical value of pH is less common in the literature, and the assessment of acidity based on those proxies is usually qualitative (e.g., acidic vs. nonacidic categorization or determination of relatively higher/lower acidity). In Fig. 8, comparisons from the literature are extended to include more locations, representing diverse chemical regimes, source influences, and meteorological conditions. Proxies introduced in Sect. 3 are compared to ISORROPIA II-predicted values of aerosol pHF using gas + aerosol inputs for four locations (southeastern US in summer, California in summer, northeastern US in winter, and Tianjin in China in summer; Table 5).
Figure 8d shows that the cation ∕ anion equivalent ratio is fundamentally limited as a proxy for aerosol pHF. The assumption applied throughout the literature is that a cation deficit (anion equivalents > cation equivalents excluding H+; ratio <1; see Sect. 3 and Table 3) indicates acidic particles, and an anion deficit (ratio >1) corresponds to alkaline particles. Consequently, a molar equivalent ratio near unity represents near-neutral conditions. Figure 8 shows clearly that these interpretations of the molar ratio are not valid. For a given cation ∕ anion equivalent ratio, predicted pHF values vary by 3–4 pHF units. All of the data with cation ∕ anion equivalent ratios near unity are predicted to be quite acidic, with pHF<3 (and often <1). The behavior in Fig. 8 is consistent with observations at locations in Canada (Murphy et al., 2017) and more broadly across the US (Lawal et al., 2018). Even the aerosol predicted by the cation ∕ anion equivalent ratio to be alkaline is actually quite acidic, with pHF<3 for almost all of the data where cation ∕ anion >1. Even if pHF underestimates pH by 2 units (the maximum underestimation in Fig. 7a,b) particles would still generally be considered acidic. Common simplifying assumptions associated with the molar ratio method that were discussed in Sect. 3.1 (e.g., considering only –NO– or –) were shown by Guo et al. (2018a) to be especially problematic in estimating pHF. Taken together, these results support prior recommendations against use of equivalent ratios as surrogates for particle acidity (Guo et al., 2018b; Hennigan et al., 2015; Lawal et al., 2018; Shi et al., 2017).
Estimates of particle acidity based on an ion charge balance are similarly problematic (Fig. 8e). A charge balance of zero, which corresponds to a cation ∕ anion equivalent ratio of unity, wrongly implies nearly neutral aerosols according to this proxy. Excess cations (negative charge balance, Eq. 13, Fig. 8e), which correspond to cation ∕ anion equivalents ratios >1, wrongly imply alkaline conditions. Figure 8 agrees with prior recommendations against using the charge balance as a proxy for particle acidity (Guo et al., 2015; Hennigan et al., 2015; Murphy et al., 2017; Winkler, 1986). The equivalent ratio and charge balance methods both suffer from the same deficiencies, which include sensitivity to limitations in the precision and accuracy of measurements, not accounting for the buffering effects of many species or the modulating effects of aerosol water, and the nonideal nature of concentrated aqueous particles, which necessitates the computation of species activity coefficients. Strong acidity, a once commonly used parameter to access aerosol acidity health impacts, is essentially an ion balance and suffers from similar limitations. A further limitation of the charge balance proxy is the use of an extensive quantity () to represent an intensive property (pH) of an aerosol distribution, which points to a major design flaw of that approach.
To our knowledge, Fig. 8f represents the first quantitative comparison between the GR (the gas ratio proxy, Table 3) and predictions of aerosol pHF. Based on the thermodynamics of gas–particle partitioning, the GR (and adjGR) relationship to pH follows a sigmoidal curve that similarly defines the partitioning of semivolatile species sensitive to pH (e.g., see Fig. 5 in Pinder et al., 2008a, for an illustration of how nitrate PM is a function of the GR and adjGR). For the northeastern US and California data, the GR follows this sigmoidal behavior and is strongly correlated with predicted pHF. Increasing GR corresponds to increasing pH, although the slope and intercept of the two datasets differ substantially since they lie on different areas of the curve. In the southeastern US, the GR results show much larger absolute values than the other locations, since HNO3 measurements were unavailable and the aerosol nitrate values were used as input for TNO3 (Guo et al., 2015). The GR in Tianjin shows no relationship with pHF (slope =0.03, r2=0.01), even though the data included complete aerosol- and gas-phase measurements. Although the GR may be highly correlated with pHF in some environments, it is not advisable to use the GR as a pHF proxy given the variability observed in Fig. 8. For example, at a given GR, the pHF range spans ∼1–4 pH units while the coefficient of determination ranges from 0.01 to 0.75 across the four locations. This suggests that a posteriori knowledge of the pHF–GR relationship is required to use the GR as a proxy for pH. The GR requires aerosol inorganic composition and measurements of both gas-phase NH3 and HNO3. Therefore, with such a dataset, pHF (or pH) can be predicted directly with one of the thermodynamic equilibrium models, which is the recommended approach.
A fundamental limiting factor in using the GR as a proxy for pH is its assumptions about free ammonia. The GR method assumes that under ammonia-poor conditions, where TNH4 is less than 2×TSO4, the aerosol is acidic and TNH4 will partition predominantly to the aerosol phase (Seinfeld and Pandis, 2016). Similarly, the method assumes that ammonia-rich conditions, which exist when TNH4 is greater than 2×TSO4, correspond to largely neutralized aerosols and significant gas-phase NH3 (Seinfeld and Pandis, 2016). While ammonia-rich particles are less acidic in terms of charge balance (Eq. 13) than ammonia-poor particles (all else being equal), a plot of pH vs. GR (Fig. S1) shows that, even in ammonia-rich conditions with a high GR, particles do not approach pH near 7. The aerosol is strongly acidic (pH <1) under ammonia-poor conditions, and a small but significant fraction of TNH4 can exist in the gas phase even though the pH is low. The fraction of TNH4 in the gas-phase approaches 0.1 while the GR <0 (corresponding to ). Likewise, the aerosol remains strongly acidic even under ammonia-rich conditions, where TNH4 exceeds the amount required to neutralize all of the TSO4 (GR >0). Even when the amount of TNH4 greatly exceeds all available TNO3 and TSO4, the aerosol remains strongly acidic (approaching a predicted pH of 3.7 as the GR approaches 50 in the Fig. S1 example). For such high gas ratios the majority of TNH4 (∼0.95) resides in the gas phase. This phenomenon is somewhat counterintuitive: it seems logical that gas-phase ammonia would react completely with acids as strong as HNO3 and H2SO4 until they were fully neutralized. However, the volatility of NH3 is an important factor that balances the extent to which it reacts with acidic components in the aerosol phase. This explains the insensitivity of aerosol pH in the southeastern US, even though sulfate levels are also decreasing while ammonia has remained steady or even increased (Weber et al., 2016).
Aerosol pH calculations based on partitioning of HNO3 and NH3 between the gas and aerosol phases show mixed results when compared to predictions by thermodynamic equilibrium models (Fig. 8a–c). In the southeastern US, the ISORROPIA and NH3 partitioning-derived pHF values are moderately correlated, with nearly all values within 1 pHF unit of the 1:1 line (Fig. 8c). In this case, the pH calculated from NH3 partitioning was systematically lower than the thermodynamic model predictions, a result that was also observed for predictions in Mexico City (Hennigan et al., 2015). In California, the pHF calculations from NH3 and HNO3 partitioning generally did not agree with the thermodynamic model predictions. The model-predicted pHF was higher (average pHF=2.67) than the calculation from NH3 (average pHF=1.64) and similar to the one based on HNO3 partitioning (average pHF=2.45). Although the pHF calculations from NH3 and HNO3 partitioning lie in the same general area of the graph in Fig. 8, they were inversely correlated with each other (, not shown), an observation that requires further investigation and likely future studies to reconcile. Keene et al. (2004) also observed disagreement between the pHF calculations from NH3 and HNO3 partitioning. In the northeastern US, the phase partitioning of HNO3 gave mixed results, as well. At times, the predicted and calculated pHF values agreed well, while at other times there were differences of ∼2–3 pHF units. The greatest discrepancies were observed at the lowest ALWC (mass fraction basis, Fig. 8b), a relationship also identified by Guo et al. (2016) and consistent with the idea that activity becomes harder to predict at lower water content (Sect. 4.1, Fig. 3). Potential problems with pHF calculated from semivolatile species partitioning have been discussed (Keene et al., 1998; Keene and Savoie, 1998; Young et al., 2013). The approach requires measurements of at least one semivolatile gas-phase species and the aerosol inorganic composition, which are input into a thermodynamic model to get the ALWC, a required component to calculate condensed-phase activities in Eq. (16) and needed to use typical Henry's law coefficients in Eqs. (17) and (18). Therefore, given the need for all these inputs, thermodynamic models should be used to directly predict pH or one of its approximations.
4.3 Recommendations on the calculation of pH by approximation and proxy
Where single-ion activity predictions are not available, the comparison based on the ambient datasets used here suggests that the best pH approximation is obtained by using Eq. (7) for pH±. However, identifying a universal H+–anion pair that best reproduces pH appears to be model dependent, with only pH± (H+, ) having the potential to be a worse estimate of pH than pHF (in the case of E-AIM). Although, on average, all of the approximate measures of pH compare similarly against pH from AIOMFAC–GLE and E-AIM, there is a strong dependence of the bias on RH that is mitigated through the use of pH± (as opposed to pHF), and for this reason it is the recommended approach when ISORROPIA, MOSAIC, EQUISOLV II or similar models are used for calculations of pH in the future. Low RH also coincides with time periods where models (both box and chemical transport models) face challenges in accurately predicting gas–particle partitioning (e.g., Guo et al., 2016; Kelly et al., 2018), thus motivating a need to properly characterize acidity under those conditions.
Based on the analyses and discussion presented in this section and Sect. 3, it is strongly recommended that proxies are avoided in the analysis of particle acidity. Some of the proxies correlate with pHF, even strongly at times, although this varies greatly with ambient conditions (T, RH), composition, and concentration. This leads to large inconsistencies across locations and even within a given observational dataset. Often, the proxies are not able to qualitatively distinguish acidic from neutral particles or to capture qualitative trends in acidity (e.g., pH increases or decreases with a given indicator). A detailed comparison with thermodynamic equilibrium model predictions constrained with aerosol and gas inputs is required to identify the periods and locations where a proxy may perform adequately, defeating the purpose of using the proxy. With the open-access and web-based availability of validated aerosol thermodynamic equilibrium models (Sect. 2.6), scientists are encouraged to use one or more of these tools in future studies of particle acidity.
The previous sections highlighted how cations and anions (along with ambient conditions) drive pH in condensed phases with a focus on equilibrium conditions and models. In addition, kinetic processes such as cation and anion dissolution influence acidity. Furthermore, the acidity of aerosols, clouds, and fogs is tightly coupled with their chemical reactivity. The pH of the atmospheric aqueous phase affects the partitioning of weakly acidic and basic gases to the condensed phase and the rate of many multiphase chemical reactions. The chemical reactions in the atmospheric aqueous phase, in turn, modulate the pH of the aqueous phase. As a result, the acidity of aerosols, cloud droplets, and fog droplets is not only determined by thermodynamic equilibrium, but also multiphase chemical kinetics. Because of the complex nature of these couplings between acidity and atmospheric aqueous-phase chemistry, these issues are presented in more detail in a companion paper currently in preparation (Tilgner et al., 2020). This section highlights some important systems where acidity interacts with, and is influenced by, condensed-phase chemical reactions.
One important example of a system with chemistry–acidity feedbacks is the multiphase oxidation of sulfur dioxide (SO2) to form particulate sulfate (S(IV)→S(VI) conversion, also referred to as “sulfur oxidation”). Sulfate makes up 15 % of PM2.5 mass globally (Sofiev et al., 2018) and is a major component of PM2.5 in areas affected by emissions from combustion of sulfur-containing fossil fuels. Multiphase reactions are the primary driving force for oxidation of SO2 to sulfate (Calvert et al., 1985). The ionization of SO2 in the aqueous phase under basic conditions enhances its uptake; the effective Henry law constant for SO2 varies 3 orders of magnitude (from 17 to 1.7×104 M atm−1) between pH 3 and pH 6 (Sander, 2015). Therefore, sulfate production, especially under acidic conditions, is largely limited by the amount of SO2 that can partition to the aqueous phase. Meanwhile, sulfate formation is a major source of acidity in aerosols, fog droplets, and cloud droplets (Calvert et al., 1985). In the absence of buffering, S(IV)→S(VI) oxidation pathways which are more effective at higher pH, such as oxidation of by O3 (Maahs, 1983; Lagrange et al., 1994) or NO2 (Lee and Schwartz, 1983; Clifton et al., 1988), will become quenched with increasing sulfate production (Fig. 9, Supplement Sect. S2). However, buffering may be significant in atmospheric waters; Collett et al. (1999), for example, demonstrated that buffering in a California fog permitted the fog pH to stay 0.3 to 0.7 pH units higher than expected, enhancing the amount of sulfate aerosol present after the fog episode by 50 %.
Another important process controlled by the acidity of the aqueous phase is the solubility of transition metal ions such as Fe(III) and Mn(II), which can catalyze S(IV) oxidation. Transition metals are ubiquitous in the atmosphere, having been observed in aerosol samples and cloud/fog/rain water collected around the globe (e.g., Bianco et al., 2017; Hsu et al., 2010). Transition metals (particularly Fe, Cu, and Mn) are active in the aqueous-phase chemistry of clouds, fogs, and deliquesced aerosols, catalyzing reactions and affecting the oxidative capacity of the condensed phase (Deguillaume et al., 2005). Due in part to variation in how transition metal emissions are generated from different source types (e.g., mechanically generated mineral dust vs. condensation/gas-to-particle conversion of gases emitted during combustion), transition metal composition/concentration and source contributions vary across the aerosol size distribution (Deguillaume et al., 2005). This has implications for the chemical environment and acidity that metals from different sources are exposed to, the reactions they participate in, and their potential impacts on human health.
The degree to which transition metals contribute to condensed-phase reactions depends on their solubility. TMI solubility typically increases as pH decreases, although the relationship between pH and metal solubility is a complex one (Spokes et al., 1994). Transition metals are often emitted as largely insoluble chemical species, and their solubility increases as the emitted particles age via exposure to acidic gases in the atmosphere. The degree to which pH affects TMI solubility depends on the origin of the particles, the degree of particle aging which alters a particle's physicochemical characteristics, and the specific metal (Deguillaume et al., 2005, 2010). Several laboratory studies have attempted to elucidate the pH dependence of transition metal solubilization for different species. Spokes et al. (1994) found that for a Saharan dust sample, the solubilization of Al and Fe, while strongly enhanced at lower pH, was nearly completely reversible with increasing pH. For an urban aerosol sample, some of the solubilized metals remained in solution with increasing pH, possibly due to complexation of the metal species with organic ligands. Manganese was found in both dust and urban particles to be soluble with decreased pH, with only limited reversibility as the pH was increased.
Acid-catalyzed reactions of hypohalous acids (HOX, where X= Br, Cl or I) in sea salt aerosols influence the oxidative capacity of the troposphere (Saiz-Lopez and von Glasow, 2012; von Glasow and Crutzen, 2014; Simpson et al., 2015). The reactions of HOX with other halogen ions can lead to the release of reactive halogen gases, which are involved in many key tropospheric reaction cycles. Reactions of S(IV) with HOX are another major contributor to sulfate formation in sea salt aerosols (Chen et al., 2016; Vogt et al., 1996; von Glasow et al., 2002). These reactions acidify the aerosol (Chen et al., 2016) but may be considered a sink of reactive halogens, in that they convert HOX to their less-reactive acid form. Reactive halogen gases act directly as important sinks of key oxidants, such as O3 and HO2, and therefore indirectly influence other linked systems HOx (= OH + HO2) and NOx (= NO + NO2) (Oltmans et al., 1989; Schmidt et al., 2016; Sherwen et al., 2016). Moreover, reactive halogen gases, especially the Cl atom, can be powerful oxidants that can rapidly react with important tropospheric organic trace gases, such as nonmethane volatile organic compounds (VOCs) and dimethylsulfide (Barnes et al., 2006; Hossaini et al., 2016).
Acidity also impacts the partitioning of weak acids, including organic acids, into aqueous aerosols and cloud/fog droplets by controlling their ionization state in the aqueous phase. The hydration of carbonyl groups in compounds that also contain pH-sensitive moieties, such as α-oxocarboxylic acids, is also highly influenced by acidity (Kerber and Fernando, 2010). Increasing acidity leads to a decrease in the effective partitioning towards the particle phase of acids and to an increase in the effective partitioning of bases, and vice versa (see Fig. 10). In the case of ionizable organic species such as organic acids, key aqueous-phase oxidants, such as OH, NO3, and O3, can react via different possible reaction pathways and kinetics with the protonated and deprotonated forms (Buxton et al., 1988; Herrmann et al., 2010, 2015; Bräuer et al., 2019). Accordingly, the overall reaction rate constant for oxidation of dissociating compounds can be largely pH dependent, especially for reaction with nitrate radicals. For organic acids, the overall rate constant typically increases with increasing pH, and more efficient oxidation can be expected under less acidic conditions. For example, the overall second-order rate constant for the reaction of nitrate radicals with formic acid (and its ionized, dissociated form) varies from close to 3.8×105 M−1 s−1 at pH =2.0 to 5.1×107 M−1 s−1 at pH =5 (Exner et al., 1994). Additionally, the increased partitioning of organic acids under less acidic conditions leads to even higher oxidations rates.
Changes in the pH of a cloud or fog droplet can result from addition of acids or bases to the solution, through partitioning from the gas phase, collision/coalescence of droplets, or aqueous reactions. The magnitude of the pH change can be strongly affected by the presence and ability of weak acids or bases to buffer against that change through proton uptake or release. A buffer is a mixture of a weak acid and its conjugate base (e.g., formic acid and formate) or a mix of a weak base and its conjugate acid (e.g., ammonia and ammonium). The magnitude of an internal buffering effect is greatest when the solution pH is equal to the pKa (pKb) of the weak acid (base) buffer. External buffering can also be important, perhaps best illustrated by the uptake of additional ammonia from the gas phase in response to a decrease in solution pH (Liljestrand, 1985; Jacob et al., 1986a, b).
The formation of secondary organic aerosol material in atmospheric aerosols via multiphase processes is strongly related to the acidity. Many atmospheric organic accretion reactions, such as aldol condensation (Noziere and Esteve, 2007; Noziere et al., 2010; Sareen et al., 2010; Li et al., 2011), hemiacetal and acetal formation (Jang et al., 2002; Kalberer et al., 2004; Shapiro et al., 2009; Loeffler et al., 2006), and esterification of carboxylic acids (Barsanti and Pankow, 2006), are acid catalyzed. The acid-catalyzed reactive uptake of epoxide species, especially isoprene epoxydiols (IEPOX) (Paulot et al., 2009; Surratt et al., 2010), to aerosol water has also emerged as a significant source of secondary organic aerosol material (Lin et al., 2012; Marais et al., 2016; Pye et al., 2013). Because the epoxidic oxygen must be protonated in concert with ring-opening, the reactive uptake of IEPOX to aqueous media is strongly pH dependent, with the reactive uptake coefficient decreasing rapidly with increasing pH for pH >1 (Gaston et al., 2014). Therefore, the rate of IEPOX secondary organic aerosol (SOA) formation is slow in cloud water because of the generally higher pH compared to particles (McNeill, 2015), but given the relatively large liquid water content of clouds, which promotes dissolution, IEPOX uptake could be significant in more acidic cloud droplets (pH 3–4) (Tsui et al., 2019).
The trend of decreasing sulfate content in clouds and aerosols across North America and Europe may have implications for partitioning of inorganic (Vasilakos et al., 2018; Shah et al., 2018) and organic gases between the gas and condensed phases, as well as the dominant mechanisms and rates of multiphase chemical processes in the atmosphere which produce PM2.5 mass, under future conditions. Implications of acidity changes for partitioning of semivolatile compounds and their multiphase chemical processing are outlined in more detail in a companion paper (Tilgner et al., 2020).
Traditionally (e.g., Sects. 4, 7.1), fine-particle pH is calculated assuming equilibrium and a uniform distribution of species across all particles. Here, the role of differences in particle size, mass transfer, and composition (including presence of organic species) in driving pH in a population of particles is highlighted.
6.1 Role of particle size and composition
The pH of aerosols varies with particle size because of the differences in the chemical composition, hygroscopicity, and gas–particle equilibration timescales between fine and coarse particles. Fine-mode aerosols are produced by new-particle formation and growth but are also directly emitted from anthropogenic as well as natural sources (dust and sea salt). At least some of the chemistry that initiates new-particle formation, and thus drives low pH for the smallest sizes, involves sulfuric acid and acid–base reactions (Kulmala et al., 2004). Anthropogenically derived fine-mode aerosols are typically composed of inorganic salts, organic species, and black carbon and are generally acidic. Fine-mode pH is sensitive to the relative amounts of nonvolatile cations (if any), sulfate, nitrate, and ammonium present in the particle phase (Fig. 2) and continuously responds to the changing concentrations of their gas-phase counterparts – , , and – as well as the ambient RH and temperature.
In contrast, coarse-mode aerosols mainly consist of sea salt and dust particles directly emitted to the atmosphere as a result of wind stress on the surface of the oceans and arid land, respectively. Sea salt and dust contain significant amounts of nonvolatile cations such as Na+, Ca2+, Mg2+, and K+, whereas, in contrast, the dominant cation in fine-mode particles is typically semivolatile ammonium. Dust, and more generally nonvolatile cations, can also originate from mechanical wear or disturbances associated with anthropogenic activity such as road, residential, and commercial construction as well as brake wear and road salt application (Philip et al., 2017; Lough et al., 2005; Kolesar et al., 2018). Both fossil fuel and biomass combustion also emit nonvolatile cations in the PM2.5 size range (Reff et al., 2009). Whether or not nonvolatile cations influence pH depends on their mixing state with deliquesced particles. In other words, particles of the same size but different compositions should be treated as external mixtures when calculating their pH. For example, equilibrium model analyses of bulk ambient aerosol observations by Guo et al. (2016) indicate that the refractory ions were externally mixed from PM1 because including those ions caused deviation between the predicted and measured nitrate partitioning. A small fraction of nonvolatile aerosol components is sometimes present in the fine mode and tends to reduce acidity. For example, K+ associated with biomass burning has been shown to cause higher pH compared to cases with very low K+ levels (Bougiatioti et al., 2016).
Sea salt and dust are naturally basic or alkaline, as they contain carbonates. The pH of ocean water (≈8) is relatively uniform and sets the pHF for unprocessed sea salt emissions (Keene et al., 1998). The pH of fresh airborne dust is more difficult to assess due to the high degree of heterogeneity in composition and its hygroscopicity; however, it is very likely that ambient dust is not acidic (has pH >7). Sea salt and dust aerosol can initially maintain high pH (above 5 and close to 7) due to the presence of carbonate (). However, the uptake of acid gases such as , HCl(g), , and results in a chemical reaction (Usher et al., 2003) such as
Reaction (R4) consumes H+ produced from the uptake of acid gases (e.g., , Reactions R1 and R2 combined), allowing the aerosol to maintain its high pH until the carbonate has been depleted via conversion to CO2(g). Once the carbonate has been depleted (a process not treated by current equilibrium models, Sect. 2.6), the dust and sea salt aerosol can become acidified by continued uptake of acid gases. Observations of aged sea salt and dust indicate an internal mixture with sulfate, nitrate, and chloride due to such reactions (Fairlie et al., 2010; Kirpes et al., 2018; Tobo et al., 2010). Freshly emitted sea salt aerosol is in the liquid state while Ca-rich dust particles are emitted as solids. Consequently, acidification of sea salt aerosol is thought to proceed more efficiently due to relatively high mass accommodation coefficients (about 0.1 or higher) for condensing acids on liquid particles compared to solid dust aerosol with much lower uptake coefficients ranging between 10−4 and 10−3 (Alexander et al., 2005; Fairlie et al., 2010). The increase in aerosol water with increasing RH and the solubilization of gaseous HCl that is present in the marine boundary layer (due to acid displacement reactions) have also been suggested as the reason for increasing acidity of sea salt aerosols with increasing RH and altitude in the marine environment (von Glasow and Sander, 2001). Further acidification of sea salt aerosols occurs via displacement of Cl− as HCl(g) due to reactions such as (Mcinnes et al., 1994; Zhao and Gao, 2008)
Although these reactions do not directly produce additional H+ ions, the resulting H+ molal concentration increases due to a decrease in the overall aerosol water content in particles containing NaNO3 and Na2SO4, which are less hygroscopic than NaCl.
Overall, atmospheric particle pH is size dependent and generally higher for coarse-mode particles due to variations in inorganic composition with particle size. Differences as large 4 pH units have been reported between fine and coarse particles (Fang et al., 2017; Young et al., 2013). Bulk PM1 and PM2.5 acidity is more similar than fine- vs. coarse-mode acidity (pHF within 1–2 units, e.g., Bougiatioti et al., 2016; Guo et al., 2017b), but submicrometer (diameter <1 µm) particles still show higher acidity than bulk PM2.5. The reason for this is the strong enrichment of aerosol with NVCs from dust and sea salt at the larger sizes (even in the fine mode) and role of sulfate in new-particle formation and surface-area-driven condensation at the small sizes (Fig. 2). While semivolatile acids and bases act to homogenize acidity across the size distribution, mass transfer limitations (next section) and the heterogeneity of emission composition lead to variation in pH with size. Significant pH changes can occur in the 1 to 2.5 µm size range (Fang et al., 2017; Ding et al., 2019). The size-dependent pH is also seen for sea salt aerosol (Fridlind and Jacobson, 2000) as well as in urban aerosols in China (Ding et al., 2019), where the fine mode is consistently 2–3 pH units lower than the coarse mode. The implications of this acidity gradient are considerable for metal solubility and the resulting impacts on public health and ecosystem productivity, as well as chemistry and semivolatile partitioning of pH-sensitive species.
6.2 Role of mass transfer
Acidity is dependent on particle composition, and particle composition can be affected by mass transfer rates that vary by particle size. For fine-mode particles, the characteristic time for particle growth or shrinkage from one equilibrium state to another after changes in RH is short enough (<1 s) to justify the assumption of thermodynamic equilibrium with respect to water uptake (Pilinis et al., 1989). In comparison, equilibration of semivolatile components (HNO3, HCl, and NH3) with the fine mode ranges from 20 min or less (Guo et al., 2018b) up to 10 h (Meng and Seinfeld 1996; Fridlind and Jacobson, 2000). In the case of coarse-mode aerosols or large accumulation-mode aerosols, mass transfer rates for semivolatile components can lead to equilibration timescales of several hours. Hanisch and Crowley (2001), for example, found vapors of HNO3 reach equilibrium through uptake by sea spray aerosols of 1–3 µm diameter within 3–10 h. In another study of remote marine aerosols, equilibrium in the coarse sea salt mode is reached quickly for NH3, but HNO3 and HCl require much longer times, on the order of 10–300 h (Fridlind and Jacobson, 2000). In this case, relatively small amounts of TNH4 partition to the coarse sea salt particles compared to much larger amounts of HNO3 needed to displace HCl to reach equilibrium. These timescales are comparable or can even exceed the lifetime of the particles, implying that some particles can be removed by deposition before equilibrium is reached (Fridlind and Jacobson, 2000). In a subsequent theoretical study, Jacobson (2005a) found that under at least some conditions equilibrium can be reached within less than 1 h by large particles (<6 µm) and within 15 min by particles <3 µm, while in several other cases coarse particles took longer to reach equilibrium. Thus, aerosols of different sizes within the fine and coarse modes may not always be in mutual equilibrium due to mass transport limitations, and equilibrium alone may not uniquely determine the distribution of condensed semivolatile gases across the particles of different sizes (Wexler and Seinfeld, 1990, 1992). Given the above, both mass transport and thermodynamics must be considered to accurately predict the distribution of semivolatile gases and the associated aerosol pH across the entire aerosol size spectrum. However, simulating mass transfer and thermodynamics for the size- and composition-distributed aerosol is computationally challenging due to numerical stiffness. There are two main sources of numerical stiffness. The first source arises from the large differences in the mass transfer timescales for particles of different sizes. Additional stiffness and nonlinearity are introduced by H+ ions in partially and fully deliquesced aerosols. In such cases, the H+ ion molal hydrogen ion concentration () plays a crucial role in the determination of equilibrium aerosol-phase state as well as in the determination of equilibrium gas-phase concentrations of HNO3, HCl, and NH3 at the particle surface for computing their driving forces for mass transfer. The characteristic timescale for H+ ions is quite short relative to other species, especially under acid-neutral or sulfate-poor conditions, where the pseudo-steady-state concentrations of H+ ions are 2 or more orders of magnitude smaller than the sum of all other cations (Sun and Wexler, 1998). Since semivolatile species in different particles of different sizes are coupled via the gas phase, the numerical solver for mass transfer would have to take time steps on the order of the shortest timescale to ensure accuracy for all the species across the entire aerosol size distribution. Such small time-steps are computationally prohibitive for common chemical transport model applications. Several attempts have been made over the past 20 years to reduce the stiffness of the system of nonlinear ordinary differential equations that describe the multicomponent, size-distributed mass transfer problem so that it could be efficiently solved (Capaldo et al., 2000; Hu et al., 2008; Jacobson, 1997, 2002, 2005a; Jacobson et al., 1996; Pilinis et al., 2000; Sun and Wexler, 1998; Zaveri et al., 2008; Zhang and Wexler, 2006).
Here, we illustrate the time evolution of size-distributed pH using the sectional MOSAIC box model with 60 size bins for a scenario (test case 14 in Zaveri et al., 2008) in which fine-mode aerosol composed of (NH4)2SO4 and coarse-mode aerosol composed of NaCl were exposed to appreciable gas-phase concentrations of H2SO4 (1 ppbv), HNO3 (15 ppbv), HCl (1 ppbv), and NH3 (10 ppbv) at 85 % RH and 298.15 K temperature (Fig. 11). While the fine mode rapidly absorbs significant amounts of these gases within the first few minutes of the simulation, it takes nearly 10 h for the aerosol composition, and hence the pH, to become uniform across the bins of different sizes. Furthermore, the displacement of HCl from the coarse mode due to HNO3 absorption occurs slowly over this time, although significant differences in the pH can be seen across the coarse-mode size bins even after 10 h. In conclusion, it is important to treat dynamic mass transfer to accurately simulate size-distributed pH and composition of aerosols. Although challenging, fully dynamic and hybrid (i.e., a combination of equilibrium for fine mode and dynamic for coarse mode) numerical methods have been implemented in 3D chemical transport models (Fast et al., 2006; Jacobson et al., 2007; Zhang et al., 2010).
6.3 Role of organic–inorganic interactions
Aerosol particles are rarely composed of a completely distinct organic-free aqueous inorganic phase and electrolyte-free organic phase – an assumption often made in air quality models for reasons of simplicity. Instead, mixed particles exist consisting of a complex mixture of organic compounds, inorganic ions, and water that may be separated into multiple liquid/solid phases (Bertram et al., 2011; Hallquist et al., 2009; Maria et al., 2004; Murphy et al., 2006; Pöhlker et al., 2012; Song et al., 2012; Zuend et al., 2010). The role of organic–inorganic interactions on the acidity of liquid/amorphous aerosol phases has been addressed in only a few studies and represents an area of research where further efforts are needed. Particle-phase acidity could be affected in multiple ways by organic–inorganic interactions: directly by means of nonideal mixing effects on the activity coefficient of H+ (and all other species) in a liquid phase of given composition; indirectly via the effect of organics on composition and the equilibrium gas–particle partitioning of water and other semivolatile components (including NH3, inorganic and organic acids), as well as the potential for liquid–liquid phase separation (LLPS); and directly by dissociating organic acids that contribute dissolved H+ or amines that associate with H+.
A phase-separated particle typically consists of a rather hydrophobic organic-rich phase and an aqueous electrolyte-rich (salt/ion-rich) phase (You et al., 2014, and references therein) (Fig. 12). Note that water and inorganic ions, including H+, can exist in the organic-rich phase of a liquid–liquid phase-separated system (Pye et al., 2018; Zuend and Seinfeld, 2012). The detection of LLPS and pH in ambient particles as well as micrometer-sized droplets in laboratory experiments is a difficult technical challenge (Wei et al., 2018). To our knowledge, no online measurement techniques applicable to field sampling exist for that purpose (see Sect. 7.1 for aerosol pH measurement challenges). The current state of knowledge is therefore limited to relatively simple laboratory systems and theoretical considerations. Dallemagne et al. (2016) used a model system in the form of a super-micrometer-sized ternary aqueous poly(ethylene glycol)-400 (PEG-400) + ammonium sulfate droplet. They studied this system in a RH- and temperature-controlled cell with confocal microscopy in the presence of a pH-sensitive fluorescent dye to determine the pH value at different locations in the liquid drop. They report a small, yet distinct, change in pH due to the phase transition from a single phase to two liquid phases for this system when RH decreases: pH in a single mixed phase at >90 % RH, while the organic-rich shell phase in a LLPS state exhibited pH at 80 % RH to pH at 65 % RH; the pH in the sulfate-rich phase was not determined during LLPS. The pH value of the organic-rich phase was similar to that of a corresponding salt-free aqueous PEG-400 solution measured using a standard pH probe. Since changes in RH lead to changes in particle water content, here causing the LLPS, the degree to which such changes affected the measured pH in the Dallemagne et al. (2016) study remains unclear.
Losey et al. (2016) controlled the pH in aqueous solution droplets consisting of 3-methylglutaric acid, ammonium sulfate, and sodium hydroxide. They found that changes in pH and the degree of methylglutaric acid dissociation (deprotonation) affect the separation RH (SRH), the onset of LLPS during dehumidification. The SRH was ∼79 % for pH =3.65, ∼70 % for pH =5.17, and ∼64 % for pH =6.45. The RH at which the two liquid phases merge into a homogeneous single phase was observed around 80 % RH in this system, approximately independent of pH – indicating that a hysteresis between SRH and merging RH occurs for pH close to neutral but not at lower pH. While this study did not attempt to measure the pH in distinct liquid phases, it indicates that the established pH, resulting from interactions between inorganic electrolytes and organic acids, affects the LLPS behavior. Losey et al. (2018) further explored similar systems at higher acidity in the presence of sulfuric acid (varying the ammonium-to-sulfate ratio from 2.0 to 1.5 to 1.0). They report that all observed RH levels of phase transitions were affected by the pH established with sulfuric acid. The SRH consistently decreased with increasing amounts of sulfuric acid (toward lower pH); e.g., for 3-methylglutaric acid + ammonium sulfate + sulfuric acid from SRH of ∼80 % at pH =2.68 to SRH of ∼30 % at pH =0.34. Similar lowering of SRH with increasing acidity was also found for a nonacidic organic mixture component (1,2,6-hexanediol). Furthermore, at high acidity (here pH lower than 0.5), several of the studied systems did not show any LLPS down to very low RH. While the quantitative phase transition behavior depends on the organic component, these experiments by Losey et al. (2018) imply that organic–inorganic interactions can have an impact on mutual solubility and phase transitions, in those cases with increasing mutual solubility towards higher acidity.
While a LLPS will impact the acidity in coexisting liquid phases, the extent to which the pH values will typically differ between the phases – and, related to that, the molar concentrations of hydronium ions and ionic strength – remains an open question. Theoretical considerations aid in constraining the range of expectations in this case. Thermodynamic equilibrium between two liquid phases, each of neutral electric charge, implies that the electrochemical potential of H+ ions is equivalent in both phases (see Sect. 2). Therefore, the activity-based pH in coexisting phases is expected to be similar but not necessarily of the exact same value. Computations with the AIOMFAC-based liquid–liquid equilibrium model confirm for case studies that the pH in two liquid phases is of the same order of magnitude, often with a difference of less than 0.2 pH units (Pye et al., 2018). However, H+ molalities (or concentrations) in the two coexisting phases of atmospheric aerosols are predicted to be very different, often by up to several orders of magnitude; hence, it is important to calculate pH based on H+ activity and not simply concentration (see also Sect. 4.3 recommendations for approximating pH). In Pye et al. (2018), several thermodynamic models were applied to predict the partitioning of ammonia, water, and organic compounds between the gas and particle phases for conditions in the southeastern US during summer 2013. AIOMFAC-based coupled liquid–liquid and gas–particle partitioning computations within that study predicted partial to complete miscibility among organic and inorganic aerosol components, depending on RH. The AIOMFAC-based model predicted an increase in the concentration of gas-phase ammonia (NH3) alongside a decrease in acidity when partial miscibility of organics was accounted for. In comparison to calculations with complete phase separation between organic and inorganic ions enforced, the interactions of inorganic ions with organic compounds (in mixed phases) were predicted to promote an enhanced association of H+ and into , resulting in a slightly higher pH (0.1 pH units median increase), since the bisulfate ion is predicted to be more miscible with organic compounds than equivalent amounts of H+ and (Pye et al., 2018). This indicates a pH buffering effect of the degree of bisulfate dissociation; however, additional complexity in understanding the main drivers of such pH changes arises from simultaneous changes in the equilibrium gas–particle partitioning of water, organics, and ammonia.
The impact of amines and organic acids on H+ is usually neglected in efforts to model pH. Amines may contribute to aerosol alkalinity – especially given their potentially strong proton affinity (Dall'Osto et al., 2019), but they must be in sufficient quantities to compete with NH3 and other cations. Although not strong sources of protons or cations, these alkaline and acidic organics may still be considered together with other water-soluble organic compounds (WSOCs) in the particulate phase in terms of their ability to influence the aerosol water content. The uptake of water due to organic components is often used to correct the solvent volume and pHF derived based on the inorganic aerosol composition (e.g., Guo et al., 2015; Bougiatioti et al., 2016). This implies that aerosol pH is reversibly influenced by the amount of water (driven by RH and composition) associated with the aerosol particles, which has been shown to drive some of the diurnal variability of pH (Guo et al., 2015).
For systems where a single mixed aerosol phase is assumed, current work indicates dissociating organic acids do not strongly affect pH, and the limited studies to date suggest that inorganic species drive pH (Battaglia et al., 2019; Song et al., 2018; Vasilakos et al., 2018). For the southeastern US, pH changes predicted by E-AIM were generally limited to <0.2 pH units in response to dramatic increases in oxalic acid (Vasilakos et al., 2018). Similarly, E-AIM predicted that increases in oxalic acid concentrations resulted in <0.1 pH unit changes for polluted Beijing conditions (Song et al., 2018). This is notable since the predicted pH in Beijing (neglecting organics) was consistently above the first acid dissociation constant (pKa1) value for oxalic acid, conditions where pH is predicted to be most sensitive to organic acids (Nah et al., 2018). Nah et al. (2018) showed that for aerosol pHF varying between 0.9 and 3.8, the inorganic-only predicted pHF was sufficient to define an effective sigmoid curve for oxalic acid, one of the most abundant of organic acids with a pKa that is well within this range. Neglecting the effects of oxalate on pH by Nah et al. (2018) did not seem to affect the quality of the partitioning. Battaglia Jr. et al. (2019) extended these prior studies to include additional organic acids (oxalic, glutaric, and malonic acids) as well as three nonacid organics (levoglucosan, tetrahydrofuran, and 1-pentanol) mixed with inorganics representative of Beijing winter haze and eastern US summertime compositions. The changes in pH relative to the inorganic-only system were predicted by AIOMFAC to be quite small, generally <0.2 pH units, when a single aerosol phase was present (Battaglia Jr. et al., 2019). The response of pH to the same organics at lower RH (<70 %) or under LLPS conditions was not characterized.
While current work suggests organic–inorganic interactions only slightly affect the pH, they can drive both LLPS and other phase transitions. Based on case studies (Pye et al., 2018; Battaglia Jr. et al., 2019), the interactions between water and ions are likely the main determinants of the resulting pH value. However, considering the complexity and variability of realistic aerosol compositions, the extent to which organic–inorganic interactions moderate the pH in liquid phases has not yet been studied in depth.
The preceding sections (e.g., Sect. 2.5) have alluded to some of the distinct challenges associated with particle and cloud pH measurements. Measuring the pH of nominally sub-10 µm atmospheric aerosols is not routinely possible, as the methods typically available for bulk condensed phases (e.g., electrochemical pH probes) cannot be applied to the liquid phase of a single particle or a population of particles as a result of the extremely low levels of liquid water. Another issue is the highly concentrated nature of aerosol solutions, whose ionic strengths are often orders of magnitude above the maximum ionic strength currently accepted by the IUPAC definition (0.1 M). As a result, limited direct measurements of aerosol pH exist (Sect. 7.1.1–7.1.2), and observationally constrained estimates of bulk fine-particle acidity are usually created from thermodynamic models (Sect. 7.1.3–7.1.4). The sample volumes for fog/cloud water or precipitation are orders of magnitude larger than for aerosols and can be collected from clouds using well-established instrumentation. This, together with their dilute concentration, allows for a direct cloud water pH measurement, which has been done with electrochemical pH probes for decades (Sect. 7.2).
7.1 Observed aerosol acidity
Challenges associated with measuring semivolatile species (Sect. 3.3) and maintaining aqueous concentrations found in ambient particles have limited direct measurements of aerosol pH for many years. The abundance of many nonvolatile ionic components of the atmospheric aerosol (e.g., sulfate or sodium) can be measured. However, unperturbed equilibrium contact with the gas phase cannot be easily maintained. Determining H+ activity (or molality in the case of pHF) requires knowledge of water content, which for nonglassy aerosol is in chemical equilibrium with the gas phase (e.g., Seinfeld and Pandis, 2016). Thus, if the ALWC changes between sampling and analysis, as often occurs in routine monitoring networks, the pH of that particle can shift. A second challenge is that one of the most important cations present in submicrometer aerosol, , is largely in equilibrium with gas-phase NH3, so perturbations during collection and processing may result in large evaporation/condensation biases (e.g., Guo et al., 2018a).
Despite the obstacles related to measuring the pH of aerosols, the importance of aerosol pH has motivated efforts to more directly probe the pH of aerosols. Direct measurements may either provide an ensemble or bulk average pH value (Li and Jang, 2012; Jang et al., 2008; Ganor et al., 1993; Craig et al., 2018), single-particle values (Craig et al., 2017; Rindelaub et al., 2016b), or intraparticle pH values (Wei et al., 2018). Considerable effort has also been spent to develop pH estimates using a combination of thermodynamic modeling with measurements of aerosol- and gas-phase composition (e.g., Guo et al., 2018a, 2017a, 2015; Bougiatioti et al., 2016; Song et al., 2018; and others).
7.1.1 Bulk pH measurements
For bulk pH values to be reasonable, composition and partitioning of semivolatiles among the particles in the population should be relatively uniform (see Sect. 6 for a discussion on the role of particle mixing state). For a set of submicrometer particles with homogeneous composition (i.e., an internal mixture, as often found in aged aerosols), this assumption is often satisfied, particularly at higher RH. The simplest bulk method, first utilized in the late 1980s, involved adding a known volume of water to a filter and then utilizing a standard electrochemical pH probe to infer so-called strong acidity (Koutrakis et al., 1988). As discussed here and in Sect. 3.1, given the semivolatile nature of water and nonconservative nature of the H+ ion (Saxena et al., 1993), this approach has significant shortcomings.
The use of pH-sensitive indicators has been one of the most common approaches to avoid sample modification. Although only a handful of studies have used indicators for aerosol studies, multiple approaches have been applied. Jang et al. (2008) used a Teflon filter where the dye metanil yellow was taken up by the filter prior to sampling aerosol. Particle mass was determined gravimetrically, and pH-sensitive indicators were analyzed with a UV-Visible (UV-Vis) spectrometer. Through a calculation combining mass, absorption features of the protonated (at 545 nm) and deprotonated (at 420 nm) form, and particle volume from a simultaneous aerosol size distribution, the mass of H+ was determined and then converted to pH. The RH had to be precisely controlled, since any change in water content would limit the reliability of the results. The authors noted the need for an online approach to avoid these complications. This work was expanded in Li and Jang (2012) with the use of an optical flow chamber to help control the RH and improve transfer from the collection point in a Teflon aerosol chamber to the UV–Vis spectrometer for measurement. For a tightly controlled system, the dyed filter approach provided particle pH, but the method has not been reliably applied in the complex ambient atmosphere.
Colorimetric methods have been utilized at different points to determine the pH of aerosols and cloud droplets. Ganor et al. (1993) used pH paper on a four-stage impactor (>10, 3.0–10.0, 0.9–3.0, and <0.9 µm) to probe larger haze particles in Israel under conditions with RH exceeding 80 %, cloud droplets, and fog droplets. Two types of pH paper were used covering two pH ranges, 0.5–5.0 and 5.0–9.0 (indicator not given), with 0.5 pH unit resolution. For these measurements, a size dependence in acidity was observed, with pH decreasing from 5 to 2 from cloud/fog to large particles using visual identification. Submicrometer haze aerosol pH was characterized as having an overall pH of 1.5–2.5 in Israel (Ganor et al., 1993). Craig et al. (2018) recently quantified the measurement of aerosol pH with a precision of 0.1 pH units using particles impacted on pH paper followed by rapidly taking a cell phone picture later analyzed with a simple image processing script in MATLAB. For their work, thymol blue (pH =0–2.5) and methyl orange (pH =2.5–4.5) indicator dyes on paper were used for both model aerosol in the laboratory and ambient samples at a forested site in northern Michigan (pH =1.5–3.5) and in Ann Arbor, Michigan (pH =3.0–3.5). Water and ammonia volatilization due to increased surface-area-to-volume ratios in smaller particles explains the observed increase in particle acidity with decreasing particle size but also the inadequacy of the pH paper method to measure the pH of very small particles (Craig et al., 2018). Ganor et al. (1993) and Craig et al. (2018) mentioned that for the colorimetric approach to be effective, the particles must be aqueous with sufficient aerosol water to substantially wet the indicator paper, which was not always the case for ambient sampling. The atmospheric samples in northern Michigan (Craig et al., 2018) covering three size ranges (2.5–5.0, 0.4–2.5, and <0.4 µm) and measuring to smaller sizes than in Ganor et al. (1993) showed a distinct decrease in pH toward smaller size. For the smallest stage in Craig et al. (2018), variation in pH was observed across the samples with values ranging from 1.5 to 3.0, possibly due to differences in pH between individual particles in that size range, though further investigation is needed (see Sect. 6 for a discussion on the relationship between particle size and pH). Craig et al. (2018) made comparisons to the bulk solutions with the thermodynamic model E-AIM, finding good agreement. When applied to the particle data, the thermodynamic model ISORROPIA predicts a pHF lower than measured by roughly a pH unit, while E-AIM was roughly 2 pH units lower. Further testing is needed between thermodynamic models and colorimetric methods to explore differences, particularly since the high ionic strengths in particles may affect organic dye activity (e.g., via issues raised in Sect. 2.5).
7.1.2 Single-particle pH measurements
Several emerging methods have the potential to provide even greater insight into the pH of individual particles but have been focused on model systems. Determining single-particle pH is desirable as the variation of pH values for individual particles from the population-level average is not well known. Even a few acidic particles can dominate the average pH value for a population in an environment with fresh emissions (e.g., urban area) where the particles have not reached equilibrium with the gas concentrations surrounding them (Craig and Ault, 2018). This heterogeneity may be less important in a regional background that has experienced significant atmospheric processing (Guo et al., 2018a). One of the first approaches to single-droplet pH measurement was that of Ganor (1999), which impacted cloud and fog droplets collected on the four stages of a cascade impactor on to a cleaved calcite (CaCO3) crystal. If an acidic droplet containing sulfate was impacted, the microchemical reaction produced gypsum (CaSO4•2H2O) crystals. Fog droplet pH values of 3.0 and 4.0 were observed in Israel for sizes of 1–2 and 3–9 µm, respectively. A second single-particle method (Dallemagne et al., 2016), used for studying liquid–liquid phase separation (LLPS) in larger particles (10–30 µm) with optical microscopy methods, applied a fluorescent indicator (Oregon Green 488 carboxylic acid, succinimidyl ester) to probe pH before and after phase separation via fluorescence microscopy (see Sect. 6.3 for discussion of organic species and their role in acidity).
A recently developed approach for probing the pH of individual droplets is the acid-conjugate base method (Rindelaub et al., 2016b), which calibrates the peak area for the acid and conjugate base measured with Raman microspectroscopy to molar concentrations, which along with the acid dissociation constant (Ka) and activity coefficient calculations can be used to determine the activity of the H+ ion. Rindelaub et al. (2016b) originally applied this to monitoring sulfate and bisulfate in proximity to the pKa of 2. Craig et al. (2017) expanded this method to cover a range of systems (nitric acid–nitrate, bioxalate–oxalate, acetic acid–acetate, and bicarbonate–carbonate, as well as an inorganic–organic mixture). From these systems, a pH of −1 to 10 could be probed, covering the full range of atmospherically relevant particle pH (Fig. 2). The acid-conjugate base method originally made use of activity coefficients from the extended Debye–Hückel method (Rindelaub et al., 2016b) but has been expanded to other methods in subsequent publications (Craig et al., 2017). In addition to using simplistic model systems, recent work has shown that the protonation state of hydroxyl functional groups (–OH) in organic molecules from SOA formation can be used to estimate pH. Bondy et al. (2018) showed that by modulating pH the protonation state of 2-methylglyceric acid or 2-methylglyceric acid sulfate ester could be used to roughly identify the pH of a system, though further quantification is necessary to assess the accuracy of this approach. This was shown by monitoring the carbonyl (C=O) stretch of the carboxylic acid group on 2-methyl glyceric acid when protonated versus the asymmetric and symmetric vibrations of the carboxylate group (COO−) when deprotonated. While these vibrations have been successfully measured in ambient aerosols collected during the SOAS summer 2013 campaign, none of the acid-conjugate base methods has been applied on ambient aerosol to evaluate aerosol pH.
Wei et al. (2018) recently probed intraparticle pH variation using surface-enhanced Raman spectroscopy and showed pH is not always uniform within an individual particle. The researchers took the acid-conjugate base method one step further with nanoprobes by functionalizing a gold nanoparticle dimer with an indicator molecule (4-mercaptobenzoic acid) and monitoring the acid versus conjugate base form of the indicator molecule in 20 µm phosphate buffer solution droplets (pH =7–11). They showed that within a single particle, a gradient of up to 3.6 pH units could be observed between the core (higher pH) and the exterior few micrometers of the particle (lower pH) due to accumulation of protons at the air–water interface. Such substantial differences in pH within a single particle are unexpected (as they imply a large chemical potential difference of H+ ions), and further independent measurements are needed to confirm this behavior in atmospheric particles.
7.1.3 Considerations for the development of observationally derived pH estimates
Only very recently have methods for direct measurement of aerosol pH become available, and they require considerable development before they become routine and generally applied. Until now, most information generated on aerosol acidity relies on measurements of particle composition and gas-phase semivolatiles, in addition to thermodynamic equilibria or kinetic modeling (see Sect. 2.6). pHF (Table 1) is the most common approximation of pH reported in the literature. The accuracy of these estimates depends on and is evaluated by the agreement between observed and modeled gas–particle partitioning of pH-sensitive species – typically TNH4, TNO3, and TCl, as well as accuracy of predicted aerosol liquid water (Guo et al., 2015, 2017b, 2018b; Meskhidze et al., 2003; Song et al., 2018). NH3 is an ideal species to measure since gas–particle partitioning of TNH4 is sensitive to most ambient pH levels and is often the dominant particle cation. However, NH3 measurements are challenging and often not colocated with aerosol composition measurements. Bougiatioti et al. (2016) estimated that neglecting gas-phase NH3 levels of about 0.1 to 0.7 µg m−3 in the thermodynamic equilibrium calculation of fine-aerosol pH could lead to an underestimation in the pHF of around 0.5 units, while Guo et al. (2015) found neglecting gas-phase NH3 leads to an underestimation of pHF by 1 unit. Although this magnitude of underestimation is not universally applicable when NH3 is missing from the thermodynamic calculations, it may be a reasonable bound for most of the atmosphere. Weber et al. (2016) and Guo et al. (2017a) estimated that, on average, a 5-fold to 10-fold increase in the NH3 levels leads a 1-unit change in pH. For cases were more than 90 % of TNH4 is in the aerosol, neglecting gas-phase NH3 should give similar (1 unit) underestimations in pH. Accurately bounding the error requires aerosol pH calculations to be evaluated against observations in both the aerosol and gas phases.
Routine air quality monitoring networks provide limited opportunity for pH estimation. European networks (European Monitoring and Evaluation Programme (EMEP)/EBAS, http://ebas.nilu.no/, last access: 7 April 2020; and Research Infrastructure for the observation of Aerosol, Clouds and Trace Gases (ACTRIS), http://actris.nilu.no/Data/Policy/, last access: 7 April 2020) provide mainly bulk PM10 aerosol chemical composition data which prohibit equilibrium assumptions due to the contributions from coarse-mode mass. Most routine networks in the US measure PM2.5, but the Interagency Monitoring of Protected Visual Environments (IMPROVE, http://vista.cira.colostate.edu/Improve/, last access: 7 April 2020) network lacks measurements of and the Chemical Speciation Network (CSN, https://www.epa.gov/amtic/chemical-speciation-network-csn, last access: 7 April 2020) is biased low compared to other networks and measurements (Pye et al., 2018; Silvern et al., 2017). The Clean Air Status and Trends Network (CASTNET, https://www.epa.gov/castnet, last access: 7 April 2020) provides measurements of , , and , along with HNO3, SO2, and base cations, at approximately 92 sites across the US. However, CASTNET does not size-select particles. For IMPROVE and CSN, concurrent relevant gas-phase measurements are generally not available. Up until 2015, the Southeastern Aerosol Research and Characterization Study (SEARCH) in the US provided complete hourly particle and gas-phase semivolatile measurements with high accuracy and precision (Edgerton et al., 2006; Hansen et al., 2003). Recent instrumental developments (MARGA, Liu et al., 2014) enable concurrent measurements of inorganic substances that influence aerosol pH and are present in the gas phase (namely HCl, HNO3, HNO2, SO2, NH3) or in the aerosol phase (Cl−, , , , K+, Ca2+, Mg2+). Online NH3 instruments are becoming more available, with sensitivity down to very low concentrations (von Bobrutzki et al., 2010). In combination with aerosol data, gas-phase measurements generate datasets that can constrain aerosol pH.
For submicrometer aerosol (PM1), the development and operation of aerosol mass spectrometers (AMS, Zhang et al., 2007; Jimenez et al., 2009) and aerosol chemical speciation monitors (ACSMs, Ng et al., 2011) during the last decade provides a powerful tool to build a database of nonrefractory submicrometer aerosol composition. This database could constrain aerosol pH when complemented by gas-phase measurements, mainly of NH3, as well as measurements of the nonvolatile, refractory aerosol components. Such studies, usually performed on a campaign basis, have enabled the estimation of aerosol pH at various locations around the globe, including the southeastern US, Greece, and mainland China (Table S6), and ACSM measurements could be more routinely available in the future (e.g., ACTRIS, Schmale et al., 2017). However, the contribution of organosulfates and organonitrates to AMS-measured total sulfate and nitrate (Farmer et al., 2010; Dovrou et al., 2019) must be considered to provide robust inorganic aerosol composition for acidity predictions. In locations such as the eastern US in summer where organosulfates already account for 15 % of total sulfate (Riva et al., 2019), AMS-measured total sulfate, when used in a thermodynamic model as inorganic sulfate, can lead to erroneous predictions of particle composition and thus pH (Pye et al., 2018).
The largest challenge using network or campaign data to estimate pH is that simultaneous information on NH3 and is often not available. The National Atmospheric Deposition Program/Ammonia Monitoring Network (AMoN) measures NH3 on a biweekly schedule at 104 active sites in the US (as of 29 July 2019) (http://nadp.slh.wisc.edu/data/AMoN/, last access: 13 April 2020). Colocation with CASTNET measurements provides at approximately 70 sites (Puchalski et al., 2019). The UK National Ammonium Monitoring Network (NAMN) has been established to measure the spatial distribution and long-term trends in atmospheric gaseous NH3 and aerosol (Sutton, 2001; Sutton et al., 1998). In 2016, the network measured gaseous NH3 on a monthly basis by DEnuder for Long-Term Atmospheric (DELTA) sampling at 56 sites and by Adapted Low-cost Passive High Absorption (ALPHA) samplers at a further 38 sites, with 9 of these sites used for calibration, in order to quantify the spatiotemporal variability of NH3 and concentrations and deposition across the UK (http://www.pollutantdeposition.ceh.ac.uk/content/ammonia-network, last access: 8 April 2020). Observations show spatially variable changes in NH3 with both reductions, mainly to the north, and increases to the south between 1997 and 2007. In nature reserve areas in the Netherlands, atmospheric NH3 concentrations have been monitored by the Measuring Ammonia in Nature (MAN) network (http://man.rivm.nl, last access: 8 April 2020) since 2005 (Lolkema et al., 2015). In 2015 that network contained 60 natural areas with a total of 236 sampling points were NH3 was monitored using passive samplers. While no significant trend has been found on average, at six stations a significant increasing trend was recorded.
The amount of knowledge on the atmospheric distribution of NH3 has increased rapidly in the satellite era since the NH3 tropospheric column observations from space by the Atmospheric Infrared Sounder (AIRS) sensor on board the Aqua satellite (Warner et al., 2016), the Infrared Atmospheric Sounding Interferometer (IASI) (Clarisse et al., 2009), and the Cross-track Infrared Sounder (CrIS) (Shephard and Cady-Pereira, 2015) became available. These satellite observations have shown high NH3 levels associated with animal feeding operations and fertilizer applications as well as biomass burning (especially wild fires). These data provided a global view of NH3 column distribution, construction of which was inhibited by the spatial and temporal variability of NH3 concentrations reflecting its spatially varying sources and its short tropospheric lifetime of up to a couple of hours (Dentener and Crutzen, 1994). While there is not yet established methodology to derive aerosol pH from space observations, the improvement of near-surface information on atmospheric composition in combination with ground-level observation network data (perhaps even augmented by model fields of such data) will likely advance our understanding. Considerably more challenging, however, is constraining the vertical distributions of aerosol pH – especially since the lower temperatures and less abundant water progressively challenge the assumption of thermodynamic equilibrium and may require the treatment of particle history and hysteresis (e.g., Wang et al., 2008).
7.1.4 Spatial and temporal variability of aerosol pH
Current observationally constrained estimates of particle pH indicate fine-mode aerosol is ubiquitously acidic. During winter with low temperature and high relative humidity, aerosol pHF is higher than during summer following the liquid water availability and temperature (Fig. 13a). This seasonal trend has been widely observed in the eastern US (Guo et al., 2016, 2015); Beijing (Tan et al., 2018); Inner Mongolia (H. Wang et al., 2019); Hong Kong (Xue et al., 2011); the Po Valley, Italy (Squizzato et al., 2013); Cabauw, the Netherlands (Guo et al., 2018b); and eastern Canada (Tao and Murphy, 2019b), with pHF differences between seasons spanning from 0.6 to 2.3 pHF units. X. Wang et al. (2019) reported the lowest mean aerosol pHF in summer and attributed it to the higher contribution of secondary sulfate than in the other seasons and the highest mean aerosol pHF in spring likely associated with the influence of dust. The most complete dataset containing seasonality comes from Canada, where observationally derived monthly mean pH values for PM2.5 were constructed for six sites over 10 years (Tao and Murphy, 2019b). The Canadian dataset shows summertime minimum pH and wintertime maximum with 1 pH unit of difference (∼2 versus ∼3, respectively). Aerosol acidity increases with increasing temperature (0.1 unit increase in pH per 2 K decrease in temperature) and decreasing relative humidity. Summer pH is largely dictated by temperature, while both meteorological factors and aerosol composition affect winter pH. Beijing shows a similar pHF trend with winter having higher pHF than summer (pHF of 4.1 vs. 1.8) (Tan et al., 2018). However, Beijing data also show summer 2016–2017 pHF (Ding et al., 2019) being almost 2 units higher than that in summer 2014 (Tan et al., 2018), potentially indicating effective air pollution mitigation strategies. The summer minimum in fine-aerosol pH is a common feature of all available pH datasets and is associated with the effects of high ambient temperatures and low aerosol water content. Temperature has also been shown to strongly affect the partitioning of total ammonium through its effects on solubility and dissociation (Hennigan et al., 2015). Composition can also play a role in seasonality as shown in data for Inner Mongolia (H. Wang et al., 2019) and the Po Valley (Squizzato et al., 2013), where maximum fine-aerosol pHF was found in spring likely due to the influence of desert dust aerosol from the Gobi and from Sahara deserts respectively. The absolute values in Mongolia show partial neutralization of the aerosol with pHF between 5 and 6.1, while those for the Po Valley are more acidic, being 1.3 pHF units higher in spring (pHF=3.6) than in the summer (pHF=2.3).
Similarly, resulting from diurnal changes in temperature and relative humidity, higher pHF is observed during the night compared to that during the day (Fig. 13b). For example, acidity shows diurnal variation of almost 2 pHF units in China (Cheng et al., 2015), of 0.5–5 pH units in southern Canada (Murphy et al., 2017), of 0.65–1.5 pHF units in the US (Battaglia et al., 2017; Guo et al., 2015; Nah et al., 2018), and about 1 pHF unit in southern California (Guo et al., 2017b). Finokalia experiences ∼1 pHF unit lower pHF during the day than night because of low aerosol water content and high temperatures (Bougiatioti et al., 2016). This pattern is amplified by the urban heat island effect through its impact on temperature (Battaglia et al., 2017).
Figure 14 summarizes the current estimates of ambient fine-aerosol pH based on literature data summarized in Table S6. Studies that used only aerosol composition for calculating pH (reverse-mode aerosol calculations, which are uncertain; e.g., see Hennigan et al., 2015) or ion-balance based approaches are excluded from the figure. Mean fine-aerosol pHF ranges from around 1 to 6 although specific locations and episodes may experience higher or lower acidity. Highly acidic fine aerosols are found in Southeast Asia, the eastern US, and other locations. Mainland China, Europe, Canada, Mexico, and the western US have on average similar levels of aerosol acidity (2.5 to 3). This spatial variability in pH reflects variability in the chemical composition of fine aerosols that result from the combined effect of changes in sources and meteorology.
Overall, the eastern US aerosol is predicted to be one of the most acidic locations, with average pHF near a value of 1 (Battaglia et al., 2017; Craig et al., 2018; Fang et al., 2017; Weber et al., 2016; Pye et al., 2018; Xu et al., 2015; Guo et al., 2016, 2015) and higher pHF, by about 1 unit, observed in locations of intensive agriculture with high NH3 concentrations (Nah et al., 2018) and those influenced by larger particles (Fang et al., 2017; Craig et al., 2018). Higher aerosol pH (2–3 in pHF) was estimated for Los Angeles in summer (Guo et al., 2017b), similar to observationally derived values for the eastern Mediterranean (0.5–2.8 pHF, Bougiatioti et al., 2016). The pHF values of PM1 and PM2.5 in Pasadena during the CalNex 2010 campaign were slightly different with the larger PM2.5 particles having pHF 0.8 units higher than PM1 (Guo et al., 2017b) due to the larger water content and more abundant NVCs at larger sizes. Greater acidity in submicrometer (PM1) versus larger (PM2.5) fine-mode particles is a robust feature in multiple datasets (e.g., Bougiatioti et al., 2016; Fang et al., 2017; Fridlind and Jacobson, 2000; Ding et al., 2019; see Sect. 6.1 for a discussion of pH as a function of particle size). Guo et al. (2016) estimated the mean pHF at 0.77±0.96 for PM1 aerosol aloft based on aerosol chemical composition measurements during the Wintertime Investigation of Transport, Emissions, and Reactivity (WINTER) campaign in the northeastern US and thermodynamic modeling.
For mainland China, fine-aerosol pHF estimates vary but tend to be mildly acidic (average pHF approximately 4) and span from negative values (in Chengdu) to as high as 6.1 for PM2.5 aerosol (Liu et al., 2017; Jia et al., 2018; Song et al. 2018; Tian et al., 2018; Cheng et al., 2015; He et al., 2018; Tan et al., 2018; Shi et al., 2017; Guo et al., 2017a; Ding et al., 2019; Jia et al., 2018b; Wang et al., 2019), while in Southeast Asia (Singapore and Hong Kong) fine aerosol is highly acidic (average pHF approximately 1) (Behera et al., 2013; Yao et al., 2007). Ding et al. (2019) estimated coarse particles were generally neutral or alkaline, based on observations in Beijing and modeling with ISORROPIA II. The strong acidity in Southeast Asia is consistent with reported high solubility of particulate iron sampled in the South China Sea (Li et al., 2017). Altogether, these data suggest that there is a large spatial gradient of pH across China and Southeast Asia, reflecting the highly variable sources of acidity and alkalinity within each region (Shi et al., 2019).
Higher aerosol pHF of 4.60 and 4.75 has been inferred from observations for Hawaii (Pszenny et al., 2004) and for Sao Paulo (Vieira-Filho et al., 2016). In the case of Hawaii, the higher pHF is due to the neutralizing effect of nonvolatile cations from sea salt. However, more acidic particles (pH ranging from −0.8 to 3.0) have been observed near the Kīlauea volcano in Hawaii (Kroll et al., 2015). Sao Paulo is affected by combustion sources and thus emissions of nitrate and NVCs that increase the aerosol pHF. Bougiatioti et al. (2016) reported that, under the influence of biomass burning, aerosol pHF increases to values around 3, indicative of the impact of nonvolatile cations, particularly potassium, as well as ammonia and nitrate emitted from wood burning. In general, aerosol pHF increases when gas-phase NH3 increases and can further be elevated by co-condensation of nitrate and water and the presence of nonvolatile ions (Guo et al., 2018a; Shi et al., 2019).
Information on pH trends over time is limited, due to the scarcity of relevant data. pH data for mainland China published prior to 2010 (Tables S6, S7) showed highly acidic aerosol with pHF of in contrast to more recent estimates (mean pHF of 3.42±1.75 for 2011–2016). Pre-2010 estimates are subject to large uncertainty resulting from their calculation method of relying only on aerosol composition information as input. Thermodynamic analysis of data, when carried out in a way that minimizes pH biases (mostly focused on using total gas and particle composition inputs and higher RH conditions), suggests acidity trends that may, at first glance, seem counterintuitive. One of the few such examples published that provides important insights can be found for the eastern US during summer. Emissions controls over the last 20 years led to significant reduction in sulfate aerosol, and ammonia levels remained constant or even slightly increased. Despite these important changes, summertime aerosol acidity remained the same (Weber et al., 2016). The insensitivity of aerosol pH to changes in emissions controls in this region is largely driven by the semivolatility of ammonium, which requires a fraction of it to remain in the gas phase as dictated by thermodynamic equilibrium. Similar behavior was found by Tao and Murphy (2019b) in Canada, where summertime aerosol pH did not increase over 10 years despite substantial decreases in sulfate and constant levels of ammonia. In the same study, the seasonality and interannual variability of pHF were found to be strongly driven by the temperature changes and the resulting shift in thermodynamic partitioning and water uptake. The modeling study of Lawal et al. (2018) also showed little response of aerosol pHF throughout the continental US to emission reductions despite the considerable improvements in air quality over the period 2001–2011. For this, they used a thermodynamic model (ISORROPIA II) and the chemical transport model (CMAQ) together with the relevant aerosol pH observations from three monitoring networks (AMoN, SEARCH, and CASTNET). However, if sulfate aerosol continues to decrease, aerosol pH may eventually begin increasing (as proposed by Tao and Murphy, 2019b). In the southeastern US, when sulfate approaches the 0.2–0.3 µg m−3 level, small amounts of NVCs start affecting pH, causing it to increase (Weber et al., 2016). Weber et al. (2016) also calculated that only large increases in NH3 together with sulfate reductions can lead to an increase in pH. Thus, for sulfate between 0.1 and 10 µg m−3, pH approaches 2.5 when NH3 is over 10 µg m−3 and ammonium nitrate is formed. In any location, unusually high levels of NH3 (an order of magnitude above the background or higher) associated with localized emissions, (e.g., confined animal feeding operations) can also increase pH (Nah et al., 2018). For locations characterized by high levels of ammonia, strong emissions of nitrate, and/or high levels of NVCs, pH may be driven by the water uptake and the mild acidity associated with ammonium nitrate aerosol. Furthermore, meteorology (RH, T) is an important driver of pH, and meteorological trends influenced by climate change or interannual variability can dominate over any composition changes (Tao and Murphy, 2019b). The eventual response of aerosol pH to changing emissions and meteorology can be determined with models – but careful evaluation of them with in situ data is critical to ensure that they are in the correct acidity regime (e.g., Vasilakos et al., 2018; Shah et al., 2018).
7.2 Observed cloud and fog acidity
Sample collection is usually the largest challenge associated with measuring cloud droplet pH. Once obtained, the pH of collected cloud and fog water is typically measured using an electronic pH meter and a combination glass electrode. The approach to pH measurement in cloud and fog water has been similar over the past several decades. Semi-micro- or micro-electrodes are available to analyze small volumes of available fog/cloud water, with some pH microelectrodes capable of measuring as little as 10 µL of sample. The electrodes are typically calibrated using pH 4 (phthalate-based) and 7 (phosphate-based) buffer solutions, although higher and lower pH calibration buffers are also available (see also Supplement Sect. S1). Buck et al. (2002) provide an overview of key buffer requirements (stability, ionic strength, certification, low pH change with temperature) and a list of primary buffer standard compositions.
7.2.1 What determines the pH in a cloud/fog droplet?
The pH of a fog or cloud drop is determined by the balance between acids and bases in solution. The initial composition of a droplet is determined by the dissolution of soluble material contained within an aerosol particle that serves as the CCN. Further changes to composition come from subsequent scavenging of other, nonactivated, interstitial particles and from uptake of water-soluble gases and aqueous-phase reactions (Sect. 5). While early measurements of cloud and fog composition focused on inorganic species, it has become increasingly clear that organic matter also contributes significantly to droplet composition (Herckes et al., 2013) and, potentially, to droplet pH.
Uptake of gaseous carbon dioxide is an important factor governing cloud pH, especially in remote environments. Equilibration of a pure water drop with current levels of atmospheric CO2 at 298 K results in a droplet pH of approximately 5.6, a value often referred to as the pH of natural rain or cloud water. Cloud pH values above or below this value are often referred to as alkaline or acidic, respectively.
Sulfuric and nitric acids frequently make significant contributions to cloud/fog drop pH, while ammonia is typically the most abundant base. Sulfuric acid is taken up through particle scavenging, including scavenging of ammoniated sulfate particles, and is also formed in situ through aqueous-phase oxidation of sulfur dioxide. Nitric acid is a highly soluble gas, in part because of its strong acidity, which leads to nearly complete deprotonation in a cloud drop to form nitrate. Addition of nitrate to cloud water also comes from scavenging of particles containing solids or dissolved nitrate salts. These include ammonium nitrate but also calcium or sodium nitrate, which are frequently formed by reaction of nitric acid or its precursors with sea salt or soil dust particles (e.g., ten Brink, 1998; Lee et al., 2008). Cloud water ammonium is derived by uptake of gaseous ammonia, as well as from particles containing salts of ammonium with nitrate, sulfate, and organic acids. As a result of these various scavenging and oxidation pathways, it is common for cloud/fog composition to be dominated by concentrations of sulfate, nitrate, and ammonium (e.g., Weathers et al., 1988; Collett et al., 2002).
A variety of weak organic acids and bases, including carboxylic/dicarboxylic acids and amines, can also influence the pH of fog or cloud drops. Carboxylic and dicarboxylic acids are frequently reported (e.g., Kawamura and Kaplan, 1984; Weathers et al., 1988; Munger et al., 1989; Facchini et al., 1992; Collett et al., 1999; van Pinxteren et al., 2005; Boris et al., 2016) as contributors to cloud or fog acidity, even in remote environments, due to the abundance of these compounds, including formic acid, acetic acid, pyruvic acid, succinic acid, and oxalic acid, in the atmosphere. For these weak acids and bases, the extent of partitioning from the gas phase is a sensitive function of droplet pH. Partitioning of weak carboxylic acids, such as formic and acetic acids, into the aqueous phase is strongly favored at pH values above the acid's pKa value, due to the deprotonation of the acid in such high-pH solutions.
7.2.2 Recent observations of cloud/fog pH and long-term trends
Clouds and fogs have been observed to exhibit a wide range of pH values (Table S8). Typical values fall between pH 3 and 6. The most acidic observation reported was in an evaporating fog in Corona del Mar in coastal southern California, with a pH of 1.69 (Hileman, 1983). Other highly acidic pH values include 1.95 for a fog at Mt. Oyama in Japan (Mori et al., 1997); 1.94 for a fog in Dübendorf, Switzerland (Sigg et al., 1987); and 1.7 for a fog in Kahler Asten, Germany (Kroll and Winkler, 1988). Such acidic values are typically associated with large inputs of sulfuric and nitric acids, although hydrochloric acid has also been an important source of acidity in some urban areas (e.g., the Dübendorf fog). High-pH fogs or clouds have also been reported in situations with large inputs of ammonia or alkaline soil dust. For example, Collett et al. (1999) reported pH values up to 7.43 for radiation fogs in California's Central Valley, a region with high ammonia concentrations stemming from major agricultural activities. Wang et al. (2011) collected cloud water at Mt. Tai, China, and observed cloud pH values during periods of strong soil dust influence in the range of 6.5–6.7. Changing regional transport patterns and resulting variations in inputs of acids and bases to Mt. Tai clouds, however, resulted in a wide range of values between 2.56 and 7.64 overall at this site. pH as high as 7.76, in Ca2+-rich advection fogs has been observed at a roadside location near Sao Paulo, Brazil (Vasconcellos et al., 2018). Fog pH values above 7 have also been reported in polluted fogs in Kanpur, India (Kaul et al., 2011; maximum pH 8.07); in Ca2+-rich fogs in Xishuangbanna, China (Zhu et al., 2000; maximum pH 9.15); in marine-influenced clouds at Puy de Dôme, France (Deguillaume et al., 2013; maximum pH 7.6); and in other locations (see Table S8).
Figure 15 (and Table S8) depicts pH observations from locations around the globe, including observations at continental and marine locations for fogs and clouds collected by airborne and ground-based sampling platforms. Panels represent different time periods, from pre-1985 to post-2005, to highlight how strong regional changes in anthropogenic emissions, especially sulfur and nitrogen oxides, are incorporated in clouds, thus affecting pH. Measurements pre-1985 are mostly associated with studies in the United States, Europe, Japan, and Australia. More global interest and coverage was seen in the later 1980s and 1990s, with several measurement sites active in east Asia, Africa, and South America. Since 2005, there has been continued interest in cloud and fog observations in some regions, including in China and India, two countries facing increasingly severe air quality challenges. Globally, observed pH values range from highly acidic to more alkaline. While measurement locations are not constant over time, there appears to be a decrease in the incidence of more acid clouds and fogs in North America and Europe since the 1980s and early 1990s, while trends in the incidence of acid fogs and clouds in East Asia are less clear.
While the global scientific community lacks long-term monitoring programs for cloud/fog composition, there are a few locations around the world where such measurements have been made routinely, or at least periodically, over periods of a decade or more. Figure 16 shows temporal trends in cloud/fog pH from a number of sites in the United States and Japan. Fog pH values from radiation fogs in California's Central Valley show a significant increase from the 1980s to the current decade. Herckes et al. (2015) attributed the rapid pH rise in the early part of the record, particularly at sites in the southern part of the valley, to decreases in SO2 emissions. A steady climb is also apparent in cloud pH values measured at Whiteface Mountain, located in upstate New York in the northeastern US, consistent with reductions in regional NOx and SO2 emissions. Schwab et al. (2016) previously reported decreases in cloud water , , , and H+ concentrations at Whiteface Mountain of 3.8 %, 3.7 %, 2.8 %, and 4.3 % per year, respectively, over the period 1994–2013. Over this 20-year period the cloud pH increased approximately 0.4 pH units per decade. Cloud pH values have been measured at remote locations in the Luquillo Mountains on the Caribbean island of Puerto Rico since 1967. Mean values reported in several studies up through 2012 (Lazrus et al., 1970; Weathers et al., 1988; Asbury et al., 1994; Gioda et al., 2009, 2011, 2013; Reyes-Rodríguez et al., 2009; Valle-Díaz et al., 2016) fall between 4.6 and 5.8, with no apparent trend. The pH values observed and the lack of a clear trend here are consistent with the fairly clean conditions in the region. Long-term records of cloud or fog composition are even rarer in Asia. Between the 1960s and 1990s in central Japan (Fig. 16), conditions are fairly acidic, with mean pH values mostly between 3 and 4. Measurements after 2000 suggest a possible increase in cloud pH in the region. Long-term (unpublished) cloud pH measurements exist for a few locations in Japan and Taiwan; a future anticipated publication may shed more light on acidity trends in the region.
Figure 17 examines changes in cloud and fog pH measured from 1980 to present in Europe. By combining data from multiple locations, a more complete assessment of pH trends on the continent is possible. While there is considerable variability within individual record years and between years, the data overall suggest a trend toward increased pH, with values at the present time typically about 1 pH unit higher than in 1980. This increase, also seen in the US, is consistent with decreasing European emissions of key acid precursors: SO2 and NOx.
Similarities in the temporal trends of cloud pH with pH trends reported in precipitation are likely, given the obvious connections between clouds and precipitation. Vet et al. (2014) analyze a large set of precipitation measurements from around the world, considering precipitation composition and its temporal changes by region, with the analyses focused especially on the period 2000–2007. They report that changes in SO2 and NOx emissions in many regions of the globe result in measurable changes in sulfate and nitrate wet deposition that in turn produce changes in pH and H+ wet deposition. Vet et al. (2014) note that 75 % of European sites and 85 % of North American sites saw increases in precipitation pH over this time period. A more spatially heterogeneous pattern of changing precipitation pH is reported for Asia. Looking at a longer time period, Duan et al. (2016) report a decreasing average precipitation pH in China from 1999 to 2006 with pH increasing after 2006, a pattern that is the inverse of temporal trends in China's SO2 emissions.
7.2.3 pH variation across drops within a cloud/fog
Up to this point, a single pH value for a cloud or fog has been discussed. In reality, each droplet within a fog or cloud is likely to have a unique composition. Within a cloud, droplets have a range of sizes as they grow, following initial cloud drop activation on CCN, by condensation (water vapor depositing on cloud drops) and coalescence (droplets typically of different sizes impacting and forming a single, larger drop). Cloud drops form when a critical supersaturation, associated with the critical (dry) diameter of the particle, is met following Köhler theory. Köhler theory indicates that larger CCN activate at lower supersaturations and are therefore the first CCN to be dissolved in droplets. A simple model representing the initial stages of condensational growth (Twohy et al., 1989) found that larger cloud drops activate on larger CCN. Larger particles are typically mechanically generated and oftentimes are comprised of more alkaline components, including soil dust and sea salt. Smaller particles, typically made up of sulfate, nitrate, ammonium, and organic species, tend to be more acidic (Hoag et al., 1999). Given that the composition of the CCN varies with size, then the fog/cloud solute composition will vary with drop size as observed in a variety of clouds and fogs (Noone et al., 1988; Ogren et al., 1989; Munger, 1989; Bator and Collett Jr., 1997; Laj et al., 1998; van Pinxteren et al., 2016; Moore et al., 2004; Guo et al., 2012a; Herckes et al., 2013).
Other cloud physical processes also affect the solute composition as a function of cloud drop size. Because of the larger surface-area-to-volume ratio in smaller drops compared to larger cloud drops, water vapor condensation will favor more rapid growth (per unit volume) of small drops, quickly diluting their solute concentrations. Furthermore, droplets formed from smaller hygroscopic particles are much more diluted at the point of cloud droplet formation (CCN activation), compared to coarse-mode particles (e.g., Nenes and Seinfeld, 2003). Coalescence tends to occur among larger and intermediate cloud drops of sufficiently different sizes because of their different fall speeds. Thus, coalescence tends to mix the composition of the larger drops, leaving the composition of very small drops less affected by this process. The same is true for mixed phase, ice–water, clouds, where falling ice crystals capture large cloud drops most effectively. Once drops or ice crystals are large enough to fall out of the cloud (i.e., precipitation as rain or snow), removal from the atmosphere (by wet deposition) of larger drops and their dissolved solutes and trace gases will occur.
The rate of mass transfer of other trace components between the gas and aqueous (cloud/fog droplet) phases also depends upon the size of the droplet. The kinetic mass transfer coefficient often used to describe the mass transfer between the gas and aqueous phases in cloud chemistry models incorporates a representation of gas-phase diffusion and interfacial mass transfer limitations and illustrates the dependence of mass transfer on droplet size, with the overall transfer rate related to the inverse of the droplet radius (or inverse of the square of the radius) (Schwartz, 1986). This size dependence of the mass transfer coefficient can contribute to mass transfer occurring to and from droplets at variable rates across the droplet size spectrum, sometimes leading to slower aqueous concentration increases in large droplets from the uptake of soluble gas-phase species compared to smaller droplets (Ervens et al., 2003).
Measurements of pH in cloud water samples collected by size-fractionating cloud water collectors (Collett et al., 1994) revealed that pH was lower in small drops compared to large drops for clouds and fogs sampled at various locations in the United States. The variation of pH across the droplet size spectrum has important implications for aqueous-phase chemistry, especially for S(IV) oxidation to form sulfate (Seidl, 1989; Hegg and Larson, 1990; Pandis et al., 1990; Lin and Chameides, 1991; Roelofs, 1993; Fahey et al., 2005; Gurciullo and Pandis, 1997; Reilly et al., 2001; Tilgner et al., 2013; Hu et al., 2019; Rao and Collett, 1998), which increases the acidity of the drops. Bulk cloud pHF calculations (i.e., average characteristics, a common treatment in chemical transport models, Sect. 8.2) tend to underestimate the fraction of dissolved S(IV) in the form of (where S(IV) ), which causes the underestimation of sulfate production rates (Fahey and Pandis, 2003; Hegg et al., 1992; Hoag et al., 1999; Moore et al., 2004; Roelofs, 1993). This is particularly true for S(IV) oxidation by ozone (O3), since the rate constant for is several orders of magnitude larger than for . Barth (2006) found that pH variation across cloud drop sizes is also important for aqueous-phase formaldehyde oxidation forming formic acid, which, as a weak acid, can reduce the pH of the drops. Furthermore, Tilgner et al. (2013) demonstrate that a size-resolved multiphase chemistry treatment results in higher acidity production in smaller droplets, leading to more acidic, smaller CCN particles after cloud processing, while larger particles tend to be less acidic.
Both the composition and pH variation across the droplet population lead to differences in reactivity for different-size droplets. Not only does the composition of droplets vary across the size spectrum in terms of reactants/oxidants but many reactions and effective Henry's law coefficients are pH dependent (Sect. 5). Additionally, droplets of different size settle and deposit at different rates. In fogs, where the net effect of processing can be a cleansing of the atmosphere, larger droplets deposit faster than smaller ones, so those species enriched in larger droplets will be removed from the atmosphere faster than those species enriched in smaller droplets (Collett et al., 2001, 2008; Fahey et al., 2005). Nevertheless, most chemistry transport models still use a bulk water composition (i.e., average characteristics) to compute aqueous-phase chemistry. Parameterizations informed by how bulk and size-resolved pH differ can be employed to better represent aqueous-phase oxidation within clouds (see Sect. 8.2).
7.3 Need for future monitoring of cloud and aerosol pH
Although cloud and fog sampling is generally more challenging than aerosol collection, pH measurement of the collected cloud/fog water is simpler due to its much larger volume and much lower ionic strength. As a result, fogs and clouds have been sampled and their pH determined in areas around the globe with more temporal and spatial coverage than for aerosol pH. Depending on inputs of key acids and bases, cloud/fog pH has been observed to range from below 2 to greater than 7, slightly higher than, but similar to, fine-aerosol pH that ranges from below 0 to near 7. Programs designed to target reductions in acid rain have had direct impacts on cloud and fog pH, but aerosol pH has been much more constant than cloud pH in the southeastern US and southeastern Canada over time. Analysis of cloud pH observations over the past 25–30 years reveals that cloud/fog acidity in many regions has decreased as anthropogenic emissions of the important acid precursors, SO2 and NOx, have decreased. A continued rise in cloud/fog pH is likely in many regions with planned future decreases in NOx and SO2 emissions and stable or increasing NH3 emissions. Future changes in emissions could eventually be significant enough to lead to fine-aerosol pH changes as well. Increases in cloud pH are expected to enhance the solubility of gas-phase organic acids, potentially shortening their atmospheric lifetimes, while increases in aerosol pH could lead to more nitrate aerosol formation and allow previously unfavorable kinetic reactions to occur.
As emissions evolve with time, continued characterization of cloud and particle pH is needed to understand how anthropogenic activities affect condensed-phase acidity and downstream endpoints in the Earth system. Much remains to be learned about factors controlling cloud/fog pH in the atmosphere and the influence of this acidity on aqueous-phase chemistry, including the aqueous-phase uptake and oxidation of soluble gases to form secondary inorganic or organic aerosol. More detailed measurements of organic acids and bases, and their influence on cloud pH, will be increasingly important as sulfate and nitrate concentrations decline. Likewise, there is a need for more systematic monitoring of cloud and fog composition in key environments, as opposed to the more ad hoc past sampling approaches driven primarily by the objectives of process-based research. Because fogs and clouds are good integrators of atmospheric acids and bases in both the gas and particle phases, they may offer a convenient and practical basis for ongoing monitoring of atmospheric acidity. Future monitoring strategies should consider long-term monitoring at surface sites as well as periodic measurements of cloud, particle, and gas-phase composition from aircraft in order to enhance our understanding of acidity at higher altitudes in the troposphere. Future measurements should also better document heterogeneity of acidity across individual drops within a cloud/fog or aerosol population, for example by determining the size dependence of pH. Aerosol pH estimates will likely continue to be primarily based on thermodynamic models in the near future and thus require simultaneous particle- and gas-phase measurements (specifically of ammonia) to improve the spatial and temporal scales over which fine-particle pH is currently characterized.
Chemical transport models and climate models are the ultimate integrators of knowledge that link emissions to the endpoints of public health, climate, and deposition. Aerosol acidity, however, is almost never considered or reported in these large frameworks (although there are exceptions; e.g., TM4-ECPL reported model-predicted pHF for clouds and particles; Fig. S2 of Myriokefalitakis et al., 2015), so potentially large differences in acidity may be a driver of bias that has been unidentified to date. In the following section, major features of a set of models (Community Multiscale Air Quality Modeling System, CMAQ; Goddard Earth Observing System with Chemistry model, GEOS-Chem; TM4-ECPL; and the Weather Research and Forecasting Model coupled with Chemistry, WRF-Chem) are summarized in terms of fine-aerosol pHF predictions (Sect. 8.1). The cloud pHF from a subset of the CTMs listed above and the Community Atmosphere Model with Chemistry (CAM-Chem; Lamarque et al., 2012; Tilmes et al., 2015), a component of the NCAR Community Earth System Model (CESM), are also included (Sect. 8.2). Table 7 summarizes the species considered in the calculation of pH for each model displayed in this work.
8.1 Aerosol pHF
All three-dimensional CTMs presented here use thermodynamic models to predict aerosol composition, and thus PM2.5 predictions are sensitive to pHF. Thermodynamic models for the inorganic system were initially implemented to predict the gas–particle partitioning of semivolatiles including nitric acid and ammonia due to their importance in forming fine particulate matter, but later studies have leveraged the predicted acidity for acid-mediated reactions. In TM4-ECPL, the pH of clouds and aerosol water affects the equilibria and thus chemistry of organic acids as well as the partitioning of reactive nitrogen and the solubilization of the trace elements iron and phosphorus. TM4-ECPL explicitly accounts for interconversion of Fe (II) and Fe (III) and formation of oxalate (the partitioning of which is also pH-sensitive, e.g., Nah et al., 2018) that acts as a ligand and contributes to secondary organic aerosol. This chemistry has been used to understand changes in oceanic deposition of Fe and P from preindustrial, present-day, and future atmospheres (Myriokefalitakis et al., 2015, 2016) as well as with regional focus on the Mediterranean region (Kanakidou et al., 2020). The CMAQ v5.1+ (Pye et al., 2013), and GEOS-Chem v11-02+ (Marais et al., 2016) models use particle acidity, although in slightly different forms, to mediate the uptake of isoprene epoxydiols and resulting production of secondary organic aerosol in PM2.5. For purposes of acid-catalyzed particle-phase reactions, GEOS-Chem uses ISORROPIA II-predicted pHF (Marais et al., 2016), while CMAQ v5.1 and later consider the entire internally mixed fine-mode particle-phase abundance in calculating the concentration of H+ (Pye et al., 2013). In CMAQ, organic constituents act to dilute H+ (increase pHF when the solvent includes organics) relative to an externally mixed or phase-separated assumption (Schmedding et al., 2019). This leads to a moderate correlation between acidity (expressed as 10) and isoprene-derived organic aerosol constituents (r2=0.3–0.5) (Budisulistiorini et al., 2017) for the SE US, in contrast to acidity pHF estimates under an externally mixed or inorganic-only solvent assumption that shows no significant correlation with isoprene SOA (Budisulistiorini et al., 2015). The WRF-Chem model, configured with MOZART chemistry and MOSAIC aerosols with the MESA thermodynamic model, uses particle acidity to calculate SOA production from glyoxal (Knote et al., 2014). Even though aqueous production of sulfate in clouds is mediated by cloud pH, heterogeneous sulfate production on aqueous aerosol (via pathways in Fig. 9) is generally not considered in models, but future efforts may include these pathways due to model underestimates of sulfate in regions like Beijing, China (e.g., Shao et al., 2019; Cheng et al., 2016); and Fairbanks, Alaska (Molders and Leelasakultum, 2012).
Chemical transport models use a variety of thermodynamic box models depending on their needs for accuracy and efficiency or treatment of specific systems and processes. The MESA thermodynamic model is used in CTMs configured with the MOSAIC aerosol model (e.g., WRF-Chem; Fast et al., 2006). ISORROPIA II is employed in several CTMs including GEOS-Chem (v8-03-01 and later), the CMAQ (v5.0 and later) modeling system, NASA GISS, WRF Polyphemus 1.6, the Tracer Model v4 (TM4-ECPL) family of models (Appel et al., 2013; Metzger et al., 2018; Myriokefalitakis et al., 2011; Pye et al., 2009), PM-CAMx (both regular and UF versions), and some versions of WRF-Chem (e.g., Zhang et al., 2013). GEOS-Chem, CMAQ, and TM4-ECPL assume the fine particles are in metastable equilibrium with the gas phase and employ the forward (i.e., gas and aerosol precursors as input) calculation mode of ISORROPIA II to partition semivolatiles and calculate liquid water content and pHF. While stable vs. metastable assumptions strongly affect the amount of liquid water content and may influence the resulting composition of the aqueous phase, Song et al. (2018) found that calculations assuming stable and metastable state yield similar results in terms of pHF when the aerosol is deliquesced for conditions in China. The generality of this finding, especially when the complex phase diagram associated with eutectics of multiple salts is fully considered, remains to be determined.
The pH of the coarse mode is treated to varying degrees in models. TM4-ECPL (Myriokefalitakis et al., 2015) applies the equilibrium assumption to internally mixed sulfate, nitrate, ammonium, sea salt, and dust aerosols in the coarse mode after equilibrating the fine-mode aerosol. CMAQ, starting with v4.7, uses a hybrid approach to mass transfer (Kelly et al., 2010) where the internally mixed Aitken and accumulation modes are in equilibrium with the gas phase, and mass transfer with the coarse mode is treated dynamically using the difference between the ambient and equilibrium vapor pressure of semivolatiles (computed with ISORROPIA II in reverse mode in CMAQ v5.0 and later) as a driving force for condensation/evaporation (Capaldo et al., 2000). This driving force, however, is not allowed to exceed the gas-to-particle diffusional limit prescribed in CMAQ which would result in numerical instability when the aerosol pH is mildly acidic to alkaline (see Sect. 6.2 for additional discussion) (Pilinis et al., 2000). While thermodynamic models are not recommended for estimating pHF in field or laboratory applications when only particle composition is available (reverse mode, open system; see discussion in Hennigan et al., 2015, and Song et al., 2018), the reverse mode can be used for a driving force in a chemical transport model since CTMs represent a closed system, species concentrations are not subject to measurement error, and the driving force can be capped at the diffusion limitation. For coarse particles in CMAQ, H+ determined via charge balance (assuming all particulate sulfur is in the form of sulfate, Eq. 13) is output for diagnostic purposes but is not used within the model. GEOS-Chem does not perform thermodynamic calculations for coarse particles. However, it does keep track of coarse-mode sea salt and dust alkalinity, which is relevant for calculating heterogeneous reactions on coarse particles. For example, heterogeneous S(IV)+O3 only happens in the model when the sea salt and dust aerosol is still alkaline (Alexander et al., 2005). Heterogeneous reactions between hypohalous acids and halide ions (e.g., HOBr+Br−) on sea salt aerosol are acid catalyzed, so these reactions are only allowed to occur in the model after the sea salt alkalinity has been titrated (titrated coarse-mode pH is assumed to be equal to 5) (Sherwen et al., 2016). The Weather Research and Forecasting Model (Powers et al., 2017; Skamarock et al., 2008) coupled with Chemistry (WRF-Chem version 3.9.1; Fast et al., 2006; Grell et al., 2005) has four aerosol configurations, including a bulk aerosol scheme, two modal aerosol schemes, and a sectional aerosol scheme (eight or four bins). Figures 19 and 21 use the four-bin sectional aerosol scheme (bins 0.039–0.156, 0.156–0.625, 0.625–2.5, and 2.5–10 µm in diameter) with MOSAIC coupled to MOZART (Model for Ozone and Related Chemical Tracers, version 4) gas-phase chemistry and cloud water chemistry (Knote et al., 2015; Zaveri et al., 2008). Within MOSAIC, the multicomponent equilibrium solver for aerosols (MESA, Zaveri et al., 2005a) solves inorganic aerosol thermodynamics for each aerosol size bin (see also Sect. 2.6.3 for a description of MOSAIC).
Even models using the same thermodynamic algorithms can produce different pHF estimates since CTMs differ in their assumptions regarding equilibrium, mixing state, emission speciation, composition distribution across size, and chemical constituents important for driving pH (see Table 7). Especially notable are differences that occur with respect to the presence, abundance, and mixing state of nonvolatile cations, the presence of which tends to increase pHF – and may further elevate pHF by co-condensation of nitrate and its associated water uptake (e.g., Guo et al., 2018a). In TM4-ECPL, , NH3, , HNO3, and are explicitly treated. Additional cations in TM4-ECPL (for fine submicrometer and coarse modes) are specified based on the composition of mineral dust and sea salt. However, TM4-ECPL does not include Ca and Mg from dust in the fine-mode calculations, as also proposed by Ito and Feng (2010), since TM4-ECPL considers all submicrometer dust and sulfate aerosol to be externally mixed in the atmosphere. The opposite assumption is made for coarse particles in TM4-ECPL since sulfate and nitrate are produced by heterogeneous processes on coarse particles (leading to an internal mixture) and coarse-particle lifetime is short (decreasing the likelihood of distinct source plumes interacting). GEOS-Chem, employing a bulk scheme for fine aerosol, considers , , , , , Na+, Ca2+, Mg2+, and Cl− from fine-mode sea salt aerosol. Cations from dust are not included in GEOS-Chem fine-aerosol pHF calculations by default (version 12.0.0), but Ca2+ and Mg2+ from fine-mode dust aerosol (assuming 3 % and 0.6 % by mass dissolution, respectively; Fairlie et al., 2010) were added to simulations in this work (see Fig. S7). CMAQ v5.0 and later, with Aitken and accumulation modes for fine aerosol, considers nonvolatile cations from sea salt; wildfires; wind-blown dust; and anthropogenic sources such as fugitive road dust, agricultural soils, and coal combustion as described by the EPA National Emissions Inventory (NEI) and SPECIATE database (Reff et al., 2009). WRF-Chem configured as MOZART–MOSAIC represents the major aerosol species including sulfate, MSA−, , Cl−, , , Na+, and Ca2+ in the charge balance for H+ (other inorganic species, primarily dust particles, are considered inert; Sect. 2.6.3). Since HCl is not present in MOZART gas-phase chemistry, displacement of Cl− from sea salt aerosols cannot be represented.
Chemical transport model predictions of particle acidity in the literature as well as in this paper (Figs. 18–19) are expressed as pHF and assume molarity- and molality-based concentrations lead to equivalent pHF with water as the solvent (Sect. 2.2 and Jia et al., 2018). CTMs, particularly those that use ISORROPIA or assume externally mixed inorganic and organic particles, assume the solvent for H+ is water associated with inorganic electrolytes. In WRF-Chem with MOSAIC, species that do not contribute directly to the ion balance (e.g., organics and inert mass) can absorb water and thereby indirectly influence the pHF via solvent abundance. TM4-ECPL and CMAQ v5.3 can calculate pHF including solvent water associated with both inorganic and organic constituents, but in this paper, only water associated with electrolytes is considered in pHF.
The limited literature to date evaluating CTM-predicted pHF indicates agreement between models and observationally constrained estimates within 1 pHF unit or better (summarized in Table S10). Observationally constrained pHF values from the eastern US in summer at the surface (0.9±0.6, Guo et al., 2015), summer aloft (1.1±0.4, Xu et al., 2016), and winter aloft (0.8±1.0, Guo et al., 2016) all indicate strongly acidic particles and are in good agreement with the GEOS-Chem aloft predicted pHF of 1.3 during the SEAC4RS 2013 (Marais et al., 2016) and WINTER 2015 (Shah et al., 2018) campaigns. CMAQ agreement with observations in the eastern US is sensitive to assumptions regarding nonvolatile cations with surface-level predictions of pHF showing good agreement with observations in the work of Vasilakos et al. (2018) (pHF=0.82) and when nonvolatile cations were excluded in the work of Pye et al. (2018) (pH). For Centreville, Alabama, in the work by Vasilakos et al. (2018), CMAQ predicted excessively acidic aerosol during the day and similar to or higher than observationally constrained pHF estimates by 1 unit at night. Reductions in nonvolatile cations, which may be overpredicted due to errors in nocturnal mixing (Appel et al., 2013), reduced the nocturnal pHF in CMAQ, making it more consistent with observations (Vasilakos et al., 2018). pHF evaluation in other locations is more limited. Guo et al. (2017b) indicate a pHF for wintertime Beijing of 4.2, consistent with GEOS-Chem simulations of Beijing for autumn/winter (pHF=4.3, range: 3.6 to 5.0; Shao et al., 2019) and CMAQ (pHF of 4.5±0.8 for Beijing February 2016, this work). Shao et al. (2019) found that including Ca2+, K+, and Mg2+ from dust in the aerosol pHF calculations had a small effect on predicted aerosol pHF (increase of 0.1) in Beijing in autumn and winter, consistent with Guo et al. (2017b).
An evaluation of CTM-predicted pHF can be leveraged to understand the responsiveness of a model to changes in atmospheric composition. For example, Vasilakos et al. (2018) show that modeling pHF correctly in CMAQ is critical to accurately partition nitrate between the gas and aerosol phase and thus capture trends in PM2.5 nitrate as sulfate is reduced in the United States. Shah et al. (2018) provide insight into the effectiveness of past and future emission reductions by tracking pHF predicted by GEOS-Chem. Shah et al. (2018) predict that pHF for winter in the eastern US increases from 0.39 to 1.7 between 2007 and 2023 using GEOS-Chem. As a result, nitrate aerosol concentrations are predicted to decrease less than the reductions of NOx emissions and total nitrate would imply. Since regulatory guidance for model application encourages the use of relative response factors (RRFs) by the PM2.5 component (EPA, 2018), a pHF evaluation can be particularly useful since a bias in pHF can result in a bias in gas–particle partitioning sensitivity. However, absolute abundances are also important in model applications, and thus a pHF evaluation complements evaluation against speciated PM2.5 measurements from networks and intensive campaigns.
Figures 18 and 19 show results from four CTMs to give a sense of whether common spatial features exist among models predicting fine-particle pHF. Differences in fine-particle pHF between models are likely caused by differences in model resolution as well as emission and meteorology scenarios as the ISORROPIA II and MESA/MOSAIC thermodynamic models produce similar values (Sect. 4). pHF is strongly influenced by nonvolatile cations in broad regions affected by dust and sea spray. Some of the least acidic fine aerosols (4< pHF<7) are predicted in sea-spray-rich regions and where strong westerlies occur over the southern oceans just north of Antarctica. These pHF values are consistent with those of fresh sea spray shortly (minutes) after emission (pH ∼5, Keene et al., 1998). Other areas over the ocean, for example, the northern Pacific south of Alaska, show more acidic aerosol, likely influenced by sulfur from shipping in combination with lower concentrations of sea spray cations due to colder water temperatures and relatively low wind speed. For all models that include high latitudes in the domain, extremely acidic particles are predicted in the Arctic and over Greenland (pHF<1). No estimates of Arctic aerosol pHF are available in the literature, but several studies have inferred low amounts of ammonium and high acidity from proxies (Fisher et al., 2011; Croft et al., 2016), yet sources of NH3 from seabirds may neutralize particle acidity in the Arctic (Wentworth et al., 2016). Other work has noted that sulfur dioxide is able to escape scavenging more effectively during lifting than ammonia or ammonium sulfate (Park et al., 2004), thus providing for long-range transport of acidity over alkalinity. The decrease in pHF (increase in acidity) due to scavenging also appears in the westerly outflow from China (Fig. 18), consistent with the higher fraction of soluble iron found in particles collected in the region (Li et al., 2017). A similar pattern is also found in the easterly outflow region from central America (Fig. 18), although observational confirmation is still needed.
Fine-mode pHF downwind of deserts varies by model but is between 4 and 6 for dust-dominant conditions in CMAQ and GEOS-Chem. TM4-ECPL does not include Ca and Mg from dust in the fine mode (external mixture) while it considers those NVCs in the coarse-mode calculations of aerosol pH. This assumption leads to an aerosol pHF in TM4 over the Sahara of ∼2–3 for the fine mode and ∼6–7 for the coarse mode (Fig. 18c, d), further implying that dust cations, if present and internally mixed in the fine mode, can affect aerosol by ∼4 pHF units (see also Fig. S7 for GEOS-Chem fine-aerosol pH predictions with and without dust NVCs). pHF∼6–7 fine aerosols are predicted in GEOS-Chem over the Sahara and Atlantic outflow of dust, most notably in the winter and spring and to a lesser degree in the summer and fall. SO2 emissions are nonzero in Saudi Arabia (Krotkov et al., 2016), leading to lower pHF for the Middle East compared to other desert regions such as the Sahara.
Anthropogenically dominated locations, such as Europe, Asia, and the United States, show different aerosol pHF values but are universally predicted to be acidic. All the models in Fig. 18 show a gradient in pHF over Europe with locations in the northern part of western Europe (near Germany) showing higher predicted fine-aerosol pH (pHF∼2–3) compared to the Mediterranean Sea where pHF values can be less than 1 and approach 0. This gradient is consistent with enhanced ammonia in northern Europe (Clarisse et al., 2009) and the limited European pH data, which include observationally constrained estimates for Cabauw in the Netherlands (pHF∼3.6; Guo et al., 2018b); for aerosol extracts from Germany (pH ∼1–2; Scheinhardt et al., 2013); and for Finokalia, Crete (pH excluding water associated with organics; Bougiatioti et al., 2016). Predicted aerosol pHF indicates moderate acidity (pHF∼3–4) for locations such as Beijing, China, and northern India. The eastern US is one of the more acidic anthropogenically dominated locations with 0< pHF<4 (Fig. 19), consistent with or slightly higher than observationally constrained estimates (Sect. 7.1.4). The fine horizontal resolution in WRF-Chem and CMAQ continental US simulations captures localized increases in pHF due to ammonia from agricultural activity in eastern North Carolina, the Great Plains, Idaho's Snake River Valley, and California's San Joaquin Valley (Fig. 19a, d).
The MOSAIC aerosol model in WRF-Chem provides information on how predicted aerosol pHF varies among different-size aerosols with different composition (Fig. S8). The PM2.5 aerosol pHF (aerosol-water-weighted average for bins 0.039–0.156, 0.156–0.625, and 0.625–2.5 µm in diameter, Fig. 19d) shows higher values in regions where NaCl aerosol dominates (off the coast of California, over the Great Salt Lake), moderate pHF values over the Great Plains and off the East Coast, low pHF in the Ohio River Valley (due to large SOx emissions and sulfate formation), and the lowest pHF in the southwestern US (where aerosol water is low). CMAQ (Fig. 19a) predicts similar spatial trends over the US for the fine-aerosol pHF (Aitken + accumulation modes) but generally predicts less spatial heterogeneity with more acidic particles (by ∼1–2 pHF units) over the Midwest and slightly less acidic particles (by ∼1 pHF) in the southwest. GEOS-Chem and WRF-Chem exhibit differences over Nevada of 5 pHF units during summer. WRF-Chem indicates more acidic particles in the submicrometer range compared to PM2.5. The most notable differences between PM2.5 (liquid-water-weighted sum over bins 1–3) and submicrometer pHF (liquid-water-weighted sum over bins 1–2) in WRF-Chem occur over the oceans, Gulf of Mexico, and Gulf of California where predicted pHF>5.6 for the larger fine (0.6 to 2.5 µm) bin. Similar values are not seen in the smaller aerosol bins except for one plume of pHF>5.6 (in bin 2, 0.156–0.625 µm). The two smallest aerosol size bins have very similar pH values over the continent, while the largest fine bin (bin 3) has similar pH values over the continent well inland from the coast and higher pH values near the coasts over land. Similarly TM4-ECPL shows differences of about 4 pHF units between fine- (submicrometer) and coarse-mode particles from Arizona and Montana (Fig. 18c, d). Since different sources contribute differently across the size range, heterogeneity in size-resolved pHF predictions also implies mixing state assumptions in bulk schemes affect pHF estimates and a single pHF value across a broad size range does not capture the range of states present in the atmosphere (see also Sect. 6 for a discussion on mixing state).
Coarse-mode aerosol pHF in the WRF-Chem MOSAIC (aerosol size bin 4, 2.5–10 µm size range, Fig. 19e) is generally higher than PM2.5 values (Fig. 19d), especially over the oceans where NaCl dominates (note that WRF-Chem v4.1 and earlier does not include HCl, thereby producing higher aerosol pHF over oceans than expected). In the more arid regions of the southwestern US and northern Mexico, coarse-mode aerosol pHF is quite acidic, while elsewhere over the conterminous US coarse-mode aerosol pHF ranges from 1 to 6, with low values over the Ohio River Valley. Coarse-mode aerosol pHF in TM4-ECPL (Fig. 18d) shows values near 4–6 over the central-western US and Canada and pHF<2 in the eastern US. Coarse-mode aerosol pHF has similarly low values in other anthropogenic regions (part of Europe, India, and East Asia) as well as southern Africa, Indonesia, and most of South America. Over the oceans and remote regions, coarse-mode aerosol pHF predicted by TM4-ECPL has a value of 6 or greater.
8.2 Cloud pH
Compared to aerosol pH, cloud pH calculations have a longer history in CTMs and climate models, given that sulfate is the dominant secondary pollutant in fine particulate matter that is produced primarily in cloud droplets. Recent work has shown that when cloud pH increases from a combination of SOx emission controls and increasing NH3 from intensified agriculture, the efficiency at which SO2 converts to sulfate via in-cloud O3 oxidation can increase, thus reducing the effectiveness of SOx controls close to emission regions (Paulot et al., 2017).
Compared to CTMs, climate models are more limited in their treatment of semivolatile inorganic species (e.g., particulate nitrate may not be considered as in CAM5; Liu et al., 2012) but generally include sea salt and dust (even if assumed inert) as well as sulfate. Modeling studies of acid rain with regional models (Carmichael and Peters, 1986; Chang et al., 1987; Venkatram et al., 1988) and sulfate production in climate models (Barth et al., 2000; Feichter et al., 1996; Koch et al., 1999) include pH since pH dictates the rate of aqueous reactions that convert SO2 to sulfate (Sect. 5). Early global model studies (Barth et al., 2000; Feichter et al., 1996; Park et al., 2004) either prescribed cloud pH or diagnosed pH from the concentration of cloud water S(IV)∕S(VI) and assumed ammonium-to-sulfate ratio. Even recent studies (e.g., Turnock et al., 2019) may prescribe cloud pH to simulate sulfate production. In most CTMs, the calculation of cloud pHF is more comprehensive. Five such models are described here, and pHF estimates are presented in Figs. 20–21. Chemical composition tracked for cloud chemistry can be the same as or different from that used in aerosol chemistry (Table 7).
CESM2.0, including CAM6-chem (released in 2018, Figs. 20a, 21a), includes an updated tropospheric chemistry mechanism (MOZART-T1) and represents aerosols using a modal aerosol model (MAM; Liu et al., 2012, 2016) with four lognormal modes and including the species sulfate, ammonium, primary and secondary organic matter, black carbon, soil dust, and sea salt. MAM considers the thermodynamic partitioning of H2SO4 (gas) and NH3. The MAM scheme does include cloud chemistry that represents S(IV) oxidation by ozone and hydrogen peroxide to form sulfate and nonreactive uptake of HNO3 and NH3. The pH is estimated using an iterative method to solve the electroneutrality equation using OH−, , , , , , and . The pHF is determined at each chemistry time step and grid point where liquid cloud water exists.
In CMAQ, there are two varieties of the cloud chemistry module: the default cloud chemistry routine that assumes instantaneous equilibrium to describe the distribution of species between gas–aqueous–ionic forms and the routines that include kinetic mass transfer (KMT) considerations. CMAQ's default cloud chemistry module is based on the work of Walcek and Taylor (1986). pHF (Figs. 20b, 21b) is estimated throughout the course of the chemistry calculations by solving the system of nonlinear algebraic equations resulting from electroneutrality and ionic/Henry's law equilibrium assumptions. Activity coefficients, estimated with the Davies equation, are applied to ionic species in solution. For the standard chemical mechanism (i.e., five S(IV) oxidation reactions and two SOA reactions), the following species are considered in the ion balance and ionic strength calculations: H+, OH−, , , , , , , , , , Cl−, Ca2+, Na+, K+, Mg2+. Fe3+ and Mn2+, potentially important players in catalyzing aqueous S oxidation, are included in the ionic strength calculation but do not impact droplet pHF as they are assumed to be associated with generic anions, A− and B−. pHF evolves as S(IV) is oxidized to S(VI) and additional species are scavenged from interstitial aerosol, allowing species to redistribute between phases and different (non)ionic forms for the duration of cloud processing. In CMAQ's KMT family of cloud chemistry modules, individual species/ions are tracked, including [H+], and evolve dynamically, using forward and reverse reactions to represent ionic equilibria (Fahey et al., 2017). Initial pHF is estimated from known concentrations of activated aerosol species (i.e., all accumulation- and coarse-mode species) and electroneutrality.
Bulk cloud pHF calculations were first implemented into GEOS-Chem as described in Alexander et al. (2012). Prior to this, cloud pH was assumed to equal 4.5 in GEOS-Chem. In GEOS-Chem (version 12.0.0 with MERRA-2 reanalysis) (Figs. 20c, 21c), bulk cloud pHF is calculated using local concentrations of , , , , , , and . The cloud water pHF calculation utilizes the electroneutrality equation and the following forms of dissolved species (in moles L−1): , OH−, , , , , , and . The concentration of is assumed negligible, which is valid given that most pHF values are >3 where the second dissociation of sulfuric acid is virtually complete. The model assumes a cloud mass scavenging efficiency of 0.7 for , , and aerosol based on observations (Hegg and Hobbs, 1986; Hegg et al., 1984; Schumann, 1991; Sellegri et al., 2003). The concentrations of all species but in the electroneutrality equation are calculated based on cloud liquid water content, temperature, and each species' effective Henry's law constants. For example, is calculated as follows:
where activities are approximated as aqueous concentrations, KH is Henry's law constant (Reaction R1) for HNO3, Ka is the dissociation constant (Reaction R2) for HNO3, and is the partial pressure of . The resulting cubic equation is solved numerically. GEOS-Chem does not account for the effect of organic acids or cations originating from sea salt or dust (e.g., Na+, Ca2+) on cloud water pHF. HCl is also not part of the cloud pHF calculation because HCl is not yet a transported species in the standard version of the model (version 12.0.0). This can easily be implemented into the cloud pHF calculation when the chlorine chemistry in GEOS-Chem is updated (X. Wang et al., 2019).
Cloud pHF in GEOS-Chem (Figs. 20c, 21c), as well as other models, is utilized for the calculation of sulfate production rates from in-cloud oxidation of . Bulk schemes, such as those described above, tend to underestimate sulfate production compared to calculations accounting for heterogeneity in pH with drop size (see Sect. 7.2.3 for a discussion of drivers of heterogeneity). To account for this bias, GEOS-Chem utilizes parameterizations developed by Fahey and Pandis (2001) and Yuen et al. (1996). The Fahey and Pandis (2001) parameterization is a decision algorithm that determines whether or not cloud droplet heterogeneity will impact sulfate production rates. The impact of cloud droplet heterogeneity on sulfate production rates tends to be most prevalent in the presence of alkaline aerosols such as sea salt (Alexander et al., 2012; Fahey and Pandis, 2001). If cloud water is acidic enough, heterogeneity will not matter. The Fahey and Pandis (2001) algorithm considered this effect and identified a condition where bulk cloud pHF will underestimate sulfate production rates. GEOS-Chem corrects for this low bias in the sulfate production rate utilizing the Yuen et al. (1996) parameterization, which was developed by comparing calculated sulfate production rates from a bulk cloud model with a cloud-resolving model that accounts for cloud droplet size heterogeneity. Since the Yuen et al. (1996) parameterization was developed for warm clouds, its use is restricted to temperatures above 268 K in GEOS-Chem. Additionally, the Yuen et al. (1996) parametrization is only used in GEOS-Chem over the oceans, because the parameterization considers alkalinity typical of sea salt aerosols. The impact of cloud droplet heterogeneity on sulfate production rates was implemented into GEOS-Chem by Alexander et al. (2012).
In TM4-ECPL (Figs. 20d, 21d), in-cloud pHF is controlled by strong acids (, methanesulfonate, HNO3, ), bases (ammonium ion, ), and by the dissociations of hydrated CO2, SO2, and NH3 and of oxalic acid (Myriokefalitakis et al., 2011). Cloud droplet heterogeneity and dust and sea salt aerosol components are not considered for cloud pHF calculations.
The cloud chemistry configured with the WRF-Chem v3.9.1 with MOZART gas chemistry and four-bin MOSAIC aerosol scheme is a bulk cloud water approach that is subsequently partitioned into the four cloud water bins (which connect to the four aerosol size bins). The Fahey and Pandis (2001) aqueous chemistry scheme is implemented and calculates sulfate formation as well as formaldehyde oxidation and nonreactive uptake of nitric acid, hydrochloric acid, ammonia, and other trace gases. The pHF is found using a bisection method to solve the electroneutrality equation, which includes the following species: OH−, , , , , , , , , , , , , , , , , HCOO−, Cl−, , ClOH−, and . While trace metal ion chemistry is included in the aqueous-phase formation of sulfate, these metals are not part of the pHF calculation. The pHF is determined at each chemistry time step and grid point where liquid cloud water exists (Fig. 21e).
Model-predicted cloud droplet pHF (Figs. 20–21) reflects atmospheric sources of inorganic species, similar to fine-mode aerosol pHF, but is further modulated by the presence of clouds and abundance of condensed water. Since cloud droplets are more dilute than particles, pHF is generally higher than for fine aerosol. The Southern Ocean clouds have pHF 4.5–6, with TM4-ECPL showing more acidic cloud droplets (pHF=4.5) in the southern oceans compared to GEOS-Chem and CAM-Chem (pHF∼5–6) due to lack of sea spray and dust aerosol components in TM4-ECPL cloud pHF calculations. Cloud droplet pHF is often greater over oceans than continents at the same latitude. GEOS-Chem and CAM-Chem show slightly different north–south trends in cloud pH over the Southern Ocean, with GEOS-Chem indicating clouds decrease in acidity from Antarctica to the Equator and CAM-Chem indicating increasing acidity. One cloud water pH measurement gives a value of about 5 for off the coast of Chile/Peru (Fig. 15), but more measurements are needed, particularly in the Southern Hemisphere. Note that CAM-Chem, GEOS-Chem, TM4-ECPL, and WRF-Chem do not include dust cations in the cloud pH calculations (CMAQ does include fine and coarse dust), and deserts and their downwind areas such as the Sahara and western US (e.g., Hand et al., 2017) show diversity on the order of 3–4 pHF units among the models. Measured cloud pH over northern Africa is 6–7 (Fig. 15), consistent with CMAQ. TM4-ECPL, which does not consider dust cations in cloud pH calculations, predicts pHF<4 cloud droplets in arid regions such as over the Sahara, southwestern US, and inland Asia, where liquid cloud water may be very low. Dust regions also coincide with limited cloud coverage so aqueous chemistry is less important. Several models (CMAQ, CAM-Chem, GEOS-Chem, WRF-Chem, TM4-ECPL) correctly capture locally enhanced acidity for the cloud droplets in the vicinity of the Ohio River Valley in the eastern United States as well as in upstate New York at Whiteface Mountain, where pH has been 4.5–5.0 since 2010 (Table S11). The pHF gradient from northern to southern Europe is reversed for cloud water compared to aerosols, with Germany and Poland showing more acidic cloud droplets than over Italy and Spain (GEOS-Chem, CMAQ, TM4-ECPL). For both clouds and particles, aerosol pHF is higher in northern China (e.g., Beijing) compared to southern China (e.g., the Pearl River Delta) except in TM4-ECPL. CAM-Chem, CMAQ, GEOS-Chem, and WRF-Chem do not predict present-day average cloud droplet pHF below 3 (which is not strictly the lower limit in observed cloud pH, Fig. 15). For select locations and models (Table S11), predicted cloud pH was generally within 2 pH units of observations and often showed better agreement.
8.3 Recommendations for improving models
Evaluation of CTM predictions of fine-aerosol pHF in the literature (Table S10) suggests reasonable agreement between models and observations (pHF within 1 unit for fine aerosols). However, observed estimates of pHF (Sect. 7.1) are extremely limited in location and do not fully cover the diversity of environments and values covered by CTM predictions. Furthermore, the models that have been most evaluated (e.g., CMAQ, GEOS-Chem) tend to use a relatively complete set of inorganic species and advanced thermodynamic routines such as ISORROPIA II, but this may not reflect the entire CTM or climate model community (e.g., CAM-Chem). CTM predictions here indicate that assumptions regarding nonvolatile cations, from both dust and sea salt, play a large role in CTM predictions of pHF. Prior to the inclusion of Ca, K, and Mg ions from dust in GEOS-Chem aerosol pHF calculations (this work, Fig. S7), CMAQ and GEOS-Chem showed large pHF differences (multiple pHF units) in dust outflow regions. Similarly, cloud droplet pHF predictions varied by up to 3–4 pHF units between models in nonvolatile-cation-rich environments. Despite cloud droplets generally occupying a smaller range in pHF than particles (Fig. 2), models examined here provide no indication that cloud droplet pHF is predicted more consistently across models than aerosol pHF. Spatial and temporal variability in clouds, which are challenging to predict and represented differently across models, could contribute to some of this model variability. (Note that for 10 of the 11 cases where select models were compared to observations, models tended to systematically underestimate or overestimate rather than bracket the observed cloud pHF value, Table S11). Model-to-model differences in many locations amount to multiple pHF units, and observational constraints would be needed to evaluate models. In addition to measuring inorganic aerosol constituents and gas-phase semivolatiles to perform thermodynamic calculations, particle mixing state and cloud properties may also need to be characterized with measurements. Remote locations (including over oceans, most of the Southern Hemisphere, and likely aloft) are locations with diverse CTM predictions of cloud and particle pHF and are particularly lacking observational constraints of pHF.
Aerosol and cloud acidity are key drivers of atmospheric chemistry and processes that link emissions to impacts on air quality, human health, ecosystems, and climate. Despite their importance, limited information exists on the spatiotemporal distribution of atmospheric acidity, its drivers, and its influences. For aerosol acidity, only recently have data become available that can be used for model evaluation and improvement. This review aims to provide a comprehensive overview of the state of knowledge of atmospheric acidity, considering particulate matter as well as clouds and fogs. Apart from a review of the published literature, the study also includes a rigorous set of definitions for acidity, the methods used to measure and infer the in situ levels of acidity in each condensed-phase type, and a synthesis and critical evaluation of current estimates. Across the review, the following major messages emerge (see the sections listed for more discussion):
The various pH definitions in use for characterizing aerosol and cloud water acidity differ in important ways from each other and from the definition of pH by IUPAC, which is based on the negative base-10 logarithm of the molal activity of H+. A nomenclature is provided for the community to document how different studies calculate and express aerosol acidity. The use of the definition of pH by IUPAC (Eq. 1), involving the activity coefficient of H+, is recommended to best and consistently quantify the pH. (Sect. 2.)
Methods for measuring cloud water pH are relatively established, but methods for measuring aerosol pH remain challenging. Measuring aerosol pH is difficult due to the extremely high ionic strengths that are typically found in aqueous aerosol, the low amounts of mass, and the extreme sensitivity to environmental perturbations, as well as the chemical heterogeneity found in particles across size, location, and time. Methods for determining the pH of bulk aerosol samples and individual particles continue to be developed and will address an important measurement gap that still exists for determining the acidity of aerosol. Particularly important is the application of such methods to understand the pH environment from particle to particle and within particles, especially under conditions where the aerosol is not at equilibrium or not internally mixed. (Sects. 2, 6, 7.)
None of the observationally based aerosol acidity proxies in use today are suitable as a universal indicator of pH. Under certain conditions (strongly acidic conditions), certain proxies may be of limited use and when combined with gas-phase measurements exhibit some correlation with pH. However, the uncertainty of these proxies remains very large, and even the best ones require verification with models. The best estimates of particle pH are obtained from thermodynamic model calculations when gas–particle partitioning observations are available for evaluation as well as for constraining the calculations. These estimates generally require a thermodynamic equilibrium assumption, which is reasonable for submicrometer aerosol. Direct measurement of NH3 is extremely important, since combined with aerosol data, it provides a constraint on model-derived acidity estimates and a metric for evaluation. Other semivolatile inorganic acidic gases (like HNO3 and HCl) also provide constraints on acidity but are subject to higher uncertainty due to interaction with the coarse mode. (Sect. 3 and elsewhere.)
Different box-model-based estimates of pH using the same inputs differ on average by 0.3 pH units (but can vary up to 1 pH unit, increasing with decreasing RH) depending on the model framework used and the approach for estimating the H+ activity coefficient. When single-ion activity coefficients are unavailable, an approximation based on the mean molal activity coefficient of a relevant ion pair (e.g., γ± (H+, Cl−) yielding a pH±) can reduce the bias in acidity by up to 0.43 pH units for atmospherically relevant conditions. The ion pair that leads to the best single-ion activity coefficient for H+ may be model dependent; for example, γ± (H+, ) yields the best pH± from ISORROPIA II. (Sect. 4.)
While thermodynamic partitioning and ionic equilibria are the dominant factors that drive aerosol pH levels, models are frequently lacking H+ that is kinetically generated as a result of transient gas- and liquid-phase chemical reactions. The representation of kinetic processes is necessary to determine sulfate levels important for driving pH. The consequences of varying acidity for organic particle and cloud chemistry have only started to be investigated. (Sect. 5 and Tilgner et al., 2020)
The limited observationally constrained pH estimates to date establish that acidic aerosol is ubiquitous and can be extremely acidic (pH as low as −1 averaged over long timescales and episodically even lower). Aerosol pH depends on the size, composition, and mixing state of particles. Fine-mode aerosols are often dominated by ammonium, sulfate, nitrate, and organics and are systematically more acidic (up to 5 pH units) than coarse-mode aerosols, which are rich in nonvolatile cations originating from sea salt and dust. Most observationally constrained estimates of particle acidity to date are the approximation, pHF. Since the accuracy of pHF as a measure of pH depends on RH and composition (Sect. 6), characterization of ambient pH is incomplete. (Sect. 7.1.)
Although aerosols and clouds both tend to be acidic, the response of acidity to changes in precursor emissions is distinctly different in the two media. Published studies suggest that reductions in sulfur dioxide and nitrogen oxide emissions across the US and Canada have had little impact on aerosol pH, and pH is relatively insensitive to changes in NH3. Conversely, clouds and fogs exhibit a broad pH range that is quite sensitive to the relative abundance of H2SO4, HNO3, and NH3, with multiple locations showing increases in cloud pH as anthropogenic emissions are controlled. This is a direct consequence of the difference in liquid water content, which is higher in clouds than fine aerosols (Sect. 7).
Large-scale model variation in predicted pHF, up to 5 pH units in specific locations, is likely not driven by the thermodynamic representations in models but by the composition that feeds the thermodynamic calculations (especially the emission and microphysical interactions of nonvolatile cations with other aerosol components). For locations with observationally constrained pH estimates, agreement between models and observations can be within 1 pH unit. In addition, the global acidity distribution in models and observations can be surprisingly similar (Fig. 2). Cloud pH does not seem better constrained than aerosol pH, suggesting that there is considerable work to be done refining simulations to reach agreement with observational values and trends. Spatial gradients in CTM pH predictions (that do not coincide with availability of measurements) suggest regions where future measurements should be made. The level of agreement required between models and observations depends on the target of a specific assessment (e.g., PM sensitivity to emissions, deposition of nutrients and acidity, metal solubility). Therefore, model frameworks should evaluate their endpoint of interest (e.g., deposition, PM2.5 concentration) and consider how an error in predicted pH could lead to a bias. The error in pH may be important for some applications but not others (Sect. 8).
Perhaps one of the more important outcomes of this review is the recognition that cloud and aerosol pH emerge as an important property for influencing a wide range of CTM predictions, and therefore improvements to how aerosol and cloud pH are represented in CTMs could potentially enhance policy and programs informed by these models. pH determines the innate response of a model to emission changes; can provide insights that established approaches (evaluation of gas–aerosol composition) are not able to provide; and determines the chemical regime for PM formation, deposition, and soluble metals. Including and reporting pH (or an approximation thereof) in future studies will increase the understanding of the effects of emissions, human activity, and climate change on society and the Earth system as a whole.
|The activity of hydrogen ions in aqueous solution on a molality basis|
|The activity of H+ ions on a molarity (concentration) basis|
|The activity of H+ ions on a mole fraction basis|
|Fraction of dissociated into H+ and|
|ai||The activity of species i (usually molality based for ions in aqueous solutions)|
|ACSM||Aerosol chemical speciation monitor|
|adjGR||Adjusted gas ratio (see Table 3)|
|ALPHA||Adapted Low-cost Passive High Absorption|
|ALWC||Aerosol liquid water content (mass per volume of air)|
|AMS||Aerosol mass spectrometer|
|c⊖||The standard state (unit) molarity|
|The molarity or “molar concentration” of hydrogen ions in an aqueous solution (also written using square brackets as [H+])|
|CCN||Cloud condensation nuclei|
|CTM||Chemical transport model|
|DELTA||DEnuder for Long-Term Atmospheric sampling|
|DON||Degree of neutralization (see Table 3)|
|DSN||Degree of sulfate neutralization (see Table 3)|
|The (rational) activity coefficient of H+ based on the mole fraction concentration scale|
|Fp,i||Fraction of species i in the particle vs. particle + gas phase|
|FR||Flex ratio, identifies the NH3 emissions level at which the nitrate concentration switches from NH3-insensitive (or negative sensitivity) to positive NH3 sensitivity|
|GR||Gas ratio (see Table 3)|
|Concentration of aerosol H+ per volume of air (e.g., moles per m−3 of air)|
|determined from charge balance (see Table 3)|
|HOx||Hydrogen oxides (OH + HO2)|
|Ka||Acid dissociation constant for H|
|Kb||Acid association constant for HX or H+ + XXH+|
|KH||Dimensionless Henry's law constant|
|Kw||Activity-based equilibrium constant for the dissociation of water into H+ and OH− (see Bandura and Lvov, 2005, for tabulation of values)|
|KMT||Kinetic mass transfer|
|LLPS||Liquid–liquid phase separation|
|m⊖||The standard state (unit) molality|
|Molality of H+ (mol kg−1 solvent)|
|Mw||Molar mass of water: 0.018015 kg mol−1|
|ni||Number (e.g., moles) of species i|
|NEI||National Emissions Inventory (for the United States)|
|NOx||Nitrogen oxides (NO + NO2)|
|PAHs||Polycyclic aromatic hydrocarbons|
|PFSAs||Perfluoroalkyl sulfonic acids|
|PFCAs||Perfluoroalkyl carboxylic acids|
|pH||Hydrogen ion potential with activity coefficient and concentration expressed on a molality concentration scale (see Table 1)|
|pHc||pH on a concentration (molarity) basis|
|pHx||pH on a mole fraction basis|
|pHT||Total pH based on the molality of sulfate and bisulfate ions (see Table 1)|
|pHF||Free-ion approximation of pH obtained when the activity coefficient of H+ is unity (see Table 1)|
|pH||Approximation of pH using the mean molal ion activity coefficient of an H+ and anion X pair (see Table 1)|
|PM||Particulate matter, synonymous with aerosol|
|PM1||Particulate mass with an equivalent diameter below 1 µm|
|PM2.5||Particulate mass with an aerodynamic equivalent diameter below 2.5 µm|
|R||Universal gas constant|
|r2||Coefficient of determination|
|RRF||Relative response factor, relative change in concentration due to relative change in emission|
|SOx||Sulfur oxides (usually SO2+TSO4)|
|TMIs||Transition metal ions|
|TCl||Total chloride (sum of gas-phase hydrochloric acid and aerosol chloride)|
|TNO3||Total nitrate (sum of gas-phase nitric acid and particulate nitrate)|
|TNH4||Total ammonia (sum of gas-phase ammonia and particulate ammonium)|
|TSO4||Total particulate sulfate (sum of sulfate and bisulfate)|
|VOCs||Volatile organic compounds|
|WSOC||Water-soluble organic compounds|
|The mole fraction of H+ in the solution|
|XT||Molal sulfate ratio indicating sulfate-rich vs. sulfate-poor domain (Eq. 9)|
|Z||Charge balance on total gas and particle phases used to estimate initial amount of H+ (Eq. 19)|
|ZSR||Zdanovskii–Stokes–Robinson (method for calculation of aerosol water)|
|γi||The molal activity coefficient of species i|
|The molarity-based activity coefficient of H+|
|The mean ion activity coefficient (for monovalent acid HX)|
|ρ0||The density of the reference solvent (water)|
|Activity coefficient models||AIOMFAC, UNIFAC|
|Gas–particle thermodynamic models||AIOMFAC–GLE, ADDEM, E-AIM, EQSAM, EQUISOLV II, GFEMN, ISORROPIA II, MOSAIC, SCAPE, UHAERO|
|Three-dimensional models||CAM-Chem, CESM, CMAQ, GEOS-Chem, GISS, PM-CAMx, TM4-ECPL, WRF-Chem|
|Supporting algorithms/chemistry/databases||ASTEM, CAM6, HETV, MAM, MESA, MOZART, MTEM, SPECIATE|
|Observational datasets (networks, satellites, field campaigns)||ACTRIS, AIRS, AMoN, CalNex, CASTNET, CrIS, CSN, EMEP/EBAS, IASI, IMPROVE, MAN, NAMN, SEARCH, SEAC4RS, SOAS, WINTER|
E-AIM can be run at http://www.aim.env.uea.ac.uk/aim/ (Clegg et al., 2017).
MOSAIC is available upon request from its author (Rahul Zaveri).
ISORROPIA II is available at http://isorropia.epfl.ch (last access: 15 April 2020) (access to source code requires login provided by Athanasios Nenes upon request).
EQUISOLV II output was obtained from its creator, Mark Jacobson (email@example.com).
CAM6-Chem code is available as part of CESM available at http://github.com/ESCOMP/cesm (CESM, 2020).
CMAQ v5.2 and v5.3 code is available at https://github.com/USEPA/CMAQ (US EPA Office of Research and Development, 2020a) and at https://doi.org/10.5281/zenodo.1167892 (v5.2, US EPA Office of Research and Development, 2017) and and https://doi.org/10.5281/zenodo.3379043 (v5.3, US EPA Office of Research and Development, 2019).
GEOS-Chem code is available at https://doi.org/10.5281/zenodo.1343547 (The International GEOS-Chem User Community, 2018).
TM4-ECPL code is available from its authors (Stelios Myriokefalitakis and Maria Kanakidou) upon request.
Instructions for obtaining WRF-Chem are available at http://www2.mmm.ucar.edu/wrf/users/download/get_source.html (WRF, 2020).
Box model inputs used in Sect. 4, observed cloud and fine-aerosol pH estimates from literature (Sect. 7), and other supporting data will be deposited in electronic tabular format at https://doi.org/10.23719/1504059 (US EPA Office of Research and Development, 2020b).
The Supplement related to this article is available online and includes additional documentation for definitions of pH, methods used to estimate sulfur production as a function of pH (Fig. 9), and details regarding the proxy evaluation (Fig. 8). In addition, figures further exploring the gas ratio, suitability of pH approximations, an ISORROPIA–MOSAIC intercomparison, and additional CTM predictions are shown. Data used as box model input (idealized scenarios), to create spatial maps of particle and cloud pH, and for CTM-observation comparisons of pH are available in the Supplement. The supplement related to this article is available online at: https://doi.org/10.5194/acp-20-4809-2020-supplement.
HOTP provided overall project coordination including preparation and finalization of synthesized drafts. HOTP and AN designed the overall scope of this study. AN coordinated the Supplement. JTW and JTK led Sect. 1 on the importance of acidity with contributions from AN. AZ led Sect. 2 on definitions of pH. CH led Sect. 3 on proxies of pH. AN led Sect. 4 on the box model intercomparison. Section 4 contains significant portions of text originally created by the Sect. 2 (idealized scenario calculations) and Sect. 3 (proxy calculations) teams. VFM led Sect. 5 on the role of kinetics and mechanisms of pH. RAZ led Sect. 6 on the role of particle size and mixing state. MK and AN led Sect. 7.1 on observations of atmospheric particle pH. JLCJ led Sect. 7.2 on observations of cloud water pH. HOTP led Sect. 8 on large-scale model predictions of pH. Major messages (Sect. 9) written by AN were created at a workshop organized by HOTP and hosted at the EPA in Research Triangle Park. Authors prepared text, figures, and tables in collaboration.
The authors declare that they have no conflict of interest.
The U.S. Environmental Protection Agency through its Office of Research and Development collaborated in the research described here. The research has been subjected to Agency administrative review and approved for publication but may not necessarily reflect official Agency policy. The views expressed in this article are those of the authors and do not necessarily represent the views or policies of the U.S. Environmental Protection Agency.
We thank the EPA for funding and hosting the workshop “The State of Acidity in the Atmosphere: Particles and Clouds” and Ken Elstein, Brooke Hemming, and Randa Boykin for their assistance during the workshop. We thank Chris Nolte and Donna Schwede for helpful comments on the manuscript during EPA internal review. We are grateful to Mark Z. Jacobson for participating in the model intercomparison (Sect. 4) and for providing the results of EQUISOLV II calculations. We thank Barron Henderson for assistance with CMAQ plots, Homaira Sharif for assistance with reference formatting in the main text, and Bo Xu for help assembling the appendix. We thank Barron Henderson and Sharon Phillips for their technical leadership on EPA contracts resulting in CMAQv5.2 output for hemispheric and continental US simulations, respectively. AN was supported by the project PyroTRACH (ERC-2016-COG) funded by H2020-EU.1.1. – Excellent Science – European Research Council (ERC), project ID 726165. The work by Jeffrey L. Collett Jr. and I-Ting Ku was supported by grant number NSF-AGS-1650786. Andrew Ault acknowledges support from the National Science Foundation through CAREER grant CHE-1654149. Christopher J. Hennigan acknowledges support from the National Science Foundation through project CHE-1454763. Nicole Riemer acknowledges support from NSF AGS-1254428. Andreas Zuend acknowledges support by the Natural Sciences and Engineering Research Council of Canada (NSERC, RGPIN/04315-2014). Tao Wang acknowledges support by the Hong Kong Research Grants Council (T24-504/17-N). Rahul A. Zaveri acknowledges support from the Office of Science of the U.S. Department of Energy as part of the Atmospheric System Research program (DE-AC05-76RL01830). Maria Kanakidou acknowledges support by PANACEA (MIS 5021516) cofinanced by Greece and the European Union (European Regional Development Fund). Mary Barth acknowledges support from the National Science Foundation under Cooperative Agreement No. 1852977.
This research has been supported by the U.S. Environmental Protection Agency, the National Science Foundation (grant nos. NSF-AGS-1650786, CHE-1454763, CHE-1654149, AGS-1254428, and AGS-644998, as well as Cooperative Agreement No. 1852977), the Hong Kong Research Grants Council (grant no. T24-504/17-N), the U.S. Department of Energy (grant no. DE-AC05-76RL01830), PyroTRACH (ERC-2016-COG) funded by H2020-EU.1.1. – Excellent Science – European Research Council (ERC, project ID 726165), the Natural Sciences and Engineering Research Council of Canada (NSERC, RGPIN/04315-2014), and the Greece and European Union European Regional Development Fund (grant no. PANACEA MIS 5021516).
This paper was edited by Alma Hodzic and reviewed by two anonymous referees.
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