Photochemical aging of atmospherically reactive organic compounds involving brown carbon at the air–aqueous interface
- 1Environment Research Institute, Shandong University, Binhai Road 72, Qingdao 266237, China
- 2School of Environmental Science and Engineering, Shandong University, Binhai Road 72, Qingdao 266237, China
- 3University of Lyon, Université Claude Bernard Lyon 1, CNRS, IRCELYON, 69626 Villeurbanne, France
- 4State Key Laboratory for Structural Chemistry of Unstable and Stable Species, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
Correspondence: Lin Du (email@example.com)
Water-soluble brown carbon in the aqueous core of aerosol may play a role in the photochemical aging of organic film on the aerosol surface. To better understand the reactivity and photochemical aging processes of organic coating on the aqueous aerosol surface, we have simulated the photosensitized reaction of organic films made of several long-chain fatty acids in a Langmuir trough in the presence or absence of irradiation. Several chemicals (imidazole-2-carboxaldehyde and humic acid), PM2.5 samples collected from the field, and secondary organic aerosol samples generated from a simulation chamber were used as photosensitizers to be involved in the photochemistry of the organic films. Stearic acid, elaidic acid, oleic acid, and two different phospholipids with the same carbon chain length and different degrees of saturation, i.e. 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) and 1,2-dioleoylsn-glycero-3-phosphocholine (DOPC), were chosen as the common organic film-forming species in this analysis. The double bond (trans and cis) in unsaturated organic compounds has an effect on the surface area of the organic monolayer. The oleic acid (OA) monolayer possessing a cis double bond in an alkyl chain is more expanded than elaidic acid (EA) monolayers on artificial seawater that contain a photosensitizer. Monitoring the change in the relative area of DOPC monolayers has shown that DOPC does not react with photosensitizers under dark conditions. Instead, the photochemical reaction initiated by the excited photosensitizer and molecular oxygen can generate new unsaturated products in the DOPC monolayers, accompanied by an increase in the molecular area. The DSPC monolayers did not yield any photochemical oxidized products under the same conditions. The spectra measured with polarization modulation-infrared reflection–absorption spectroscopy (PM-IRRAS) were also consistent with the results of a surface pressure–area isotherm. Here, a reaction mechanism explaining these observations is presented and discussed. The results of PM2.5 and SOA samples will contribute to our understanding of the processing of organic aerosol aging that alters the aerosol composition.
In the marine environment, the degradation of bacteria and diatoms can produce lipids, such as phospholipids, triacylglycerides, and glycolipids, which are the lipid-containing cellular components of microorganisms (Jeffrey, 1966). Phospholipids can be transported from seawater into sea spray aerosol (SSA) directly (Collins et al., 2016). They also can be further transformed into fatty acids through heterotrophic breakdown (Li-Beisson et al., 2019; Guschina and Harwood, 2006). Long-chain saturated fatty acids, such as palmitic acid and stearic acid, correspond to major constituents of the sea surface microlayer and are also detected in marine aerosols (Marty et al., 1979; Slowey et al., 1962; Wu et al., 2015; Hu et al., 2018; Kang et al., 2017). Unsaturated fatty acids with carbon chain lengths of 18–22 carbons also dominate the organic composition of seawater samples (Jeffrey, 1966; Osterroht, 1993). Oleic acid and elaidic acid were the most abundant unsaturated acids in seawater (Osterroht, 1993). The abundance of saturated fatty acids in PM10 samples collected from the south-eastern coast of China was significantly higher than unsaturated fatty acids due to their enhanced photochemical stabilities and extensive atmospheric sources (Wu et al., 2015).
“Brown carbon” (BrC) refers to the type of light-absorbing organic aerosol material that efficiently absorbs radiation from visible to ultraviolet wavelengths in the atmosphere (Laskin et al., 2015; Andreae and Gelencsér, 2006; Pöschl, 2005). The fully dissolved organic fraction of BrC is referred to as light-absorbing water-soluble organic carbon (WSOC), while colloidal aggregates belong to water-insoluble organic carbon (WIOC). BrC can be generated from primary source, such as fossil fuel combustion and biomass burning. Multiple atmospheric reactions between gas and particle or aqueous phase also lead to secondary BrC production. The products from aqueous OH oxidation of phenolic compounds have characteristic BrC absorption spectra (Gelencsér et al., 2003; Vione et al., 2014). The SOA generated by high-NOx photooxidation and ozonolysis of monoterpenes have absorption in the wavelength range of 355–780 nm (Nakayama et al., 2013; Flores et al., 2014). Aerosol flow tube experiments suggest that the exposure of SOA particles produced from biogenic alkenes to gaseous ammonia could increase the complex refractive index (Flores et al., 2014). The addition of amino acids or ammonium ions to limonene SOA was also shown to produce BrC, which strongly absorbed visible light and fluoresced at visible and ultraviolet wavelengths (Bones et al., 2010). Typical BrC is a mixture of a large number of strongly absorbing chromophores that have unique molecular structures and evolved from non-absorbing precursors (Nguyen et al., 2012; Lee et al., 2013).
Photosensitizers in the atmosphere can absorb and convert the energy of photons into chemical energy that can facilitate reactions at aerosol surfaces (George et al., 2015). Therefore, photosensitizers can contribute to organic aerosol aging and growth when generating a triplet excited state that can oxidize hydrocarbon upon absorbing light. These photosensitized reactions have been shown in the laboratory to induce to an abiotic source of volatile organic compounds (VOCs) and secondary organic aerosols (SOA) in the marine boundary layer (Rossignol et al., 2016; Tinel et al., 2016; Bernard et al., 2016). Traces of photosensitizing species in the aerosol phase, such as imidazoles, quinones and nitrophenols also contribute to SOA formation through their promoting effect with radical reactions (Li et al., 2016; Desyaterik et al., 2013; Pillar and Guzman, 2017).
Imidazole-2-carboxaldehyde (IC) is a component of BrC (Ackendorf et al., 2017; Arroyo et al., 2018; Rossignol et al., 2014), produced through the aqueous reaction of glyoxal or methylglyoxal with ammonium sulfate (Aiona et al., 2017). Recent works suggest that IC can act as an efficient photosensitizer in autophotocatalytic aerosol growth (Aregahegn et al., 2013; Rossignol et al., 2014; González Palacios et al., 2016). For example, aerosol seeds containing IC can induce the reactive uptake of VOCs when exposed to light, leading to SOA formation (Aregahegn et al., 2013). In addition to small-molecular-weight species like IC, water-soluble organic materials with higher molecular weight like humic-like substances (HULIS) can also absorb light. HULIS have the similar properties to macromolecular humic substances, such as their amphiphilic and polyacidic nature, aromaticity, surface active properties and light absorption ability (Gelencsér et al., 2002; Graber and Rudich, 2006; Sannigrahi et al., 2006; Krivacsy et al., 2008). HULIS correspond to 10 %–35 % of fine organic materials in atmospheric aerosols and account for up to 72 % of WSOC in some ambient aerosol samples (Emmenegger et al., 2007; Feczko et al., 2007). Humic substances (HS) consist of three operationally defined components: humic acids (HA), fulvic acids, and humins. These HS represent a fraction of the molecularly uncharacterized component of dissolved organic matter in the ocean (W. Z. Zhu et al., 2017). HA in the ocean are widely believed to derive primarily from the products of marine phytoplankton degradation and less so from terrestrial sources (McCarthy et al., 1996). For primary marine aerosols, WSOC containing HULIS components was suggested to originate from bubble-bursting at the surface of seawater, which transfers organic matter into marine aerosol particles (Cavalli et al., 2004; Yu et al., 2004). HULIS exist primarily in the droplet mode with aerodynamic diameter in the range of 0.7–0.8 µm (Wang and Yu, 2017).
Atmospheric aerosol particles are a mixture of a large number of inorganic and organic compounds. The different physico-chemical properties of aerosol components result in inorganic-salt aerosols being coated with a film of surface-active organic materials (Raymond and Pandis, 2003). The structure of the organic coated aqueous aerosol can be simplified as an aqueous core-shell model (Song et al., 2013; Tervahattu et al., 2005; Ellison et al., 1999). The presence of organic film on the aerosol surface can reduce the evaporation rate of water from droplets or particles (Nguyen et al., 2017; Davies et al., 2013). The transport and uptake of chemicals between the gas and liquid phase is affected by organic coating (Donaldson and Valsaraj, 2010). The packing order and stability of films on the surface also facilitate further discussion of the uptake efficiency of marine aerosols toward atmospheric trace gases such as N2O5 and HNO3 (Bertram et al., 2018). The organic film can reduce the scavenging by larger cloud droplets and affect the lifetime of aerosols (Toossi and Novakov, 1985; Gill et al., 1983). In addition, the optical properties of the droplet can be altered by organic coating (Donaldson and Vaida, 2006).
Atmospheric aerosols may contain light-absorbing BrC in the aqueous core. BrC, which is excited by visible and ultraviolet radiation in the sunlight, can act as photosensitizer to facilitate free radical reactions and contribute to photochemical aging of organic aerosol (Smith et al., 2014; Yu et al., 2014). The photosensitized uptake of limonene was also observed for several SOA materials containing a complex mixture of photosensitive organic compounds collected from the chamber (Malecha and Nizkorodov, 2017). When aerosols containing photosensitizers such as IC and HA were exposed to isoprene, limonene, α-pinene, β-pinene and toluene in the presence of UV light, there was significant SOA formation (González Palacios et al., 2016). The gaseous products from interfacial photochemistry of organic film can act as precursors for SOA, while highly oxidized products are likely to be more water-soluble (Bruggemann et al., 2017; Alpert et al., 2017). The interfacial photochemistry of a palmitic acid monolayer involving HA as a photosensitizer has been recently investigated (Shrestha et al., 2018). Therefore, the photochemistry of such organic films is attracting increasing attention, as the photosensitized reaction initiated by atmospheric samples containing BrC has not been investigated and the associated mechanism is not understood.
Here, we investigated the interfacial photochemical properties of WSOC from three different sources: (i) IC and HA as identified proxies; (ii) SOA samples collected from a simulation chamber (regarded as a half-real atmospheric sample); and (iii) authentic PM2.5 samples. To the best of our knowledge, the photosensitized reaction of organic Langmuir films involving chamber and atmospheric samples has not been previously investigated. Fatty acids and phospholipids such as 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), 1,2-dioleoylsn-glycero-3-phosphocholine (DOPC), stearic acid (SA), elaidic acid (EA) and oleic acid (OA) were selected as proxies of low volatile organic compounds of organic aerosols. Langmuir monolayers at the air–aqueous interface were employed to mimic the organic films that coat the aqueous aerosols (Sobanska et al., 2015; Ruehl and Wilson, 2014; King et al., 2009; Sebastiani et al., 2018; Adams et al., 2016). The stability behaviour of these organic films under irradiation and the impact of photosensitizers on organic aerosol aging are presented and discussed.
2.1 Materials and solutions
The zwitterionic phospholipids (DSPC and DOPC) were acquired from Avanti Polar Lipids Inc. The fatty acids (SA, EA, and OA) were purchased from Sigma-Aldrich. All chemicals used in the experiment did not require further purification. Ultrapure water (18.2 MΩ cm) provided by a Milli-Q system (Millipore, France) was used to prepare the artificial seawater (ASW), which is a solution of multiple salts: 426 mM NaCl (≥99 %, Acros), 55.5 mM MgCl2 (99.9 %, Alfa Aesar), 29.4 mM Na2SO4 (99 %, Alfa Aesar), 10.8 mM CaCl2 (99 %, Adamas), 9.45 mM KCl (99 %, Alfa Aesar), 2.43 mM NaHCO3 (≥99.7 %, Alfa Aesar), 0.86 mM KBr (≥99 %, Acros), 0.44 mM H3BO3 (99.5 %, Innochem), 0.074 mM NaF (≥99 %, Acros), and 0.094 mM SrCl2 6H2O (≥99 %, Alfa Aesar) (Brzozowska et al., 2012, 2013). The effect of artificial seawater on stabilizing organic monolayer has been confirmed in previous studies (Li et al., 2018, 2019). The photosensitizers imidazole-2-carboxaldehyde (IC) (97 %, Alfa Aesar) or HA (>90 % fulvic acid, Aladdin) were added into the ASW with concentrations of 2.5 mM and 30 mg L−1, respectively. Five different subphases were used for our experiments: pure ASW, ASW with 2.5 mM IC, ASW with 30 mg L−1 HA, ASW with PM2.5 sample, and ASW with SOA sample. The molecular structures of DOPC, DSPC, SA, EA, and OA are provided in Fig. 1a.
2.2 Atmospheric PM2.5 sample collection and preparation
Atmospheric fine particulate matter samples were collected at the atmospheric observation station (36∘40′ N, 117∘03′ E) located in the central campus of Shandong University in January 2016. A medium-volume PM2.5 sampler (TH-150 A, Wuhan Tianhong, China) was used to collect PM2.5 samples on Isopore™ membrane filters (90 mm diameter, 0.4 µm pore size; HTTP, Merck Millipore, Germany). The flow rate of sampling was 100 L min−1. The filter samples were sealed and stored at −20 ∘C before the experiment. All the filters were dissolved into 40 mL ultrapure water with ultrasonic agitation. Sonication was performed in an ultrasonic bath with a frequency of 40 kHz and the power of 80 W. The sonication time was 15 min. Subsequently, the suspension was centrifuged at 1780 g for 40 min. The supernatant, which contains the water-soluble fraction including water-soluble organic compounds (WSOC) and inorganic ions, was re-collected by freeze-drying. The insoluble fraction separated from soluble fraction was also freeze-dried. The mass ratio of insoluble to soluble fraction is 0.91 : 1. Then, 3.3 mg of freeze-dried soluble sample was dissolved in 1000 mL artificial seawater. The concentration of PM2.5 sample in the artificial seawater is 3.3 mg L−1.
2.3 Chamber sample preparation
The laboratory SOA samples were generated from a 1 m3 FEP-Teflon film chamber at room temperature (298±2 K) and atmospheric pressure. The details of the chamber including the experimental setup and the schematic of the smog chamber facility have been previously described (Liu et al., 2019; Wang et al., 2018; J. Q. Zhu et al., 2017). To maximize and homogenize the intensity of radiation, stainless steel mirror surfaces were used as the interior wall of the chamber enclosure. The chamber was surrounded by a total of 12 black lamps (Philips TUV 36 W) with a peak intensity at 365 nm to simulate actinic UV irradiation. Purified air produced by a zero air gas generator (111-D3N, Thermo Scientific, USA) was used as background. Prior to each experiment, the chamber was cleaned by zero air for more than 4 h. Liquid droplet ammonium sulfate seed particles were injected into the chamber by nebulizing a 0.6 M ammonium sulfate ((NH4)2SO4) aqueous solution with an aerosol generator (Model 3076, TSI, USA). A customized diffusion dryer was added after aerosol generator to make sure that the (NH4)2SO4 aerosols were in solid phase in chamber. Relative humidity was about 20 % throughout the experiments, which is lower than the crystallization RH (35 %) of (NH4)2SO4 (Ng et al., 2007). The seed particle was kept at solid phase. The total gas volume in the chamber was recorded with mass flow meters (D80-8C/ZM, Beijing Sevenstar, China). Limonene (99 %, tci) was injected into the chamber by a micro syringe and was evaporated into a stream of purified air. Then, an aqueous H2O2 solution (30 wt %) was injected to the chamber and served as the OH precursor in these experiments. The concentration of H2O2 was estimated to be 4324 ppb. NO was introduced into the chamber by a gas-tight syringe. Typically, 684 ppb limonene and 5×104 cm−3 (NH4)2SO4 seed aerosols were employed. The concentration of limonene was determined by gas chromatograph equipped with flame ionization detector (GC-FID) (Agilent Technologies, GC-FID 7890B). The SOA formation of limonene photooxidation experiments was performed under high-NOx condition (Sarrafzadeh et al., 2016). The initial concentration of NOx and NO detected by NO–NO2–NOx analyser (Model 42C, Thermo Electron Corporation, USA) were 206 and 164 ppb, respectively. The reaction was allowed to proceed for 4 h before SOA particles were collected. At that time, the concentration of limonene could not be detected. The initial concentrations of reactants in the chamber were also listed in Table S1 in the Supplement. The SOA particles were collected on pieces of aluminium foil with 25 mm diameter by using a 13-stage Dekati low-pressure impactor (DLPI) (DLPI+, Dekati Ltd, Finland). The particle sizes that were collected by DLPI at a sampling flow rate of 10 L min−1 ranged from 16 nm to 10 µm. Then, all the aluminium foil substrates were combined for extraction. The SOA samples collected on the aluminium foil pieces were dissolved in ultrapure water by sonicating for 1 min in an ultrasonic bath. The extract water solution was concentrated by rotary evaporation. The residue was dried under high purity nitrogen stream. Then, the SOA sample was transferred to the artificial seawater with the concentration of 0.66 mg L−1.
2.4 Calculation of the mass absorption coefficient
The UV–vis absorption spectra of four photosensitizers were measured using a UV–vis spectrophotometer (P9, Shanghai Mapada, China). Spectra were collected using quartz cuvettes with an internal path length of 1.0 cm. Aqueous solutions of 0.006 g L−1 IC, 0.006 g L−1 humic acid, 0.01 g L−1 PM2.5 sample, and 0.01 g L−1 SOA sample were used.
The IC aqueous solution displays a major absorption peak at 288 nm, which is in agreement with previous studies (Tinel et al., 2014; Berke et al., 2019). The maximum of absorption of the SOA sample was at 286 nm, as can be seen from the absorption spectrum shown in Fig. S1 in the Supplement. Similar to the previous studies, HA and PM2.5 samples' absorptions have the main feature around 200 nm with a clearly visible hump between 250 and 300 nm (Kristensen et al., 2015). We calculate the mass-absorption coefficients (MACs) (cm2 g−1) of four samples by the following equation:
where A is the absorption, b is the length of the cuvette (1 cm), and Cm is the concentration of the dissolved reaction products (g mL−1).
In order to compare the light-absorbing properties of four samples, we estimated the light-absorbing properties of aerosols by the average MAC (〈MAC〉) over the wavelength range from λ1=200 nm to λn=700 nm) (Jiang et al., 2019).
The HA sample with 〈MAC〉200–700 nm of 64 460 cm2 g−1 is also more absorbing than the IC sample (〈MAC〉200–700 nm = 41 267 cm2 g−1), the SOA sample (〈MAC〉200–700 nm = 32 867 cm2 g−1), and the PM2.5 sample (〈MAC〉200–700 nm = 16 048 cm2 g−1).
2.5 Langmuir and irradiation experiments
Langmuir and irradiation experiments were performed in a Langmuir trough (Riegler & Kirstein GmbH, Germany). The phospholipid and fatty acid monolayers were prepared by dropping 1 mM chloroform stock solution onto the artificial seawater containing the photosensitizer. After spreading the surfactant solution, 10 to 15 min were allowed for the evaporation of solvent before compression and subsequent measurements. Both the surface pressure and molecular area of the Langmuir monolayers were measured with the Wilhelmy plate method during the barrier compression at a constant barrier speed of 3 mm min−1. A Wilhelmy plate is a rectangular plate made of filter paper with a few centimetres in length and height. The plate is attached to a force sensor on the one side of barrier. In the measurement procedure, the Wilhelmy plate is first dipped into the liquid and then pulled back to the position of first contact to measure the surface pressure (Rame, 1997; Hyvärinen et al., 2006; Aumann et al., 2010). The surface pressure was obtained based on the following equation:
where γ0 is equal to the surface tension of the solution and γ is the surface tension due to the monolayer. A Plexiglass cover was used to guarantee that the experimental condition was relatively sealed. All the surface pressure–area measurements were repeated at least three times to ensure consistent results (see for example Fig. S2). The change in surface pressure at the same molecular area was measured within ±2 mN m−1. The standard deviation of the molecular area was ±1 Å2/molecule. For area relaxation measurements, the changes in relative molecular area (A∕A0) with time were also recorded, where A is the measured molecular area and A0 is the initial area for the DOPC monolayer when the compression to 25 mN m−1 was reached. The irradiation experiments were also conducted at the surface pressure equilibrium of 25 mN m−1. The trough was illuminated by three UV lights (Philips TUV TL-Mini 8 W) with peak intensity at 365 nm. The lamps were located above the Langmuir trough at a distance of 20 mm. Pure water is relatively transparent to the near-infrared and near-ultraviolet wavelengths of light. Dissolved salts in seawater have no light absorption under visible light, but slight absorption under ultraviolet light (Carpenter and Nightingale, 2015). The irradiation and non-irradiation experiments were conducted with or without the photosensitizers.
2.6 Polarization modulation-infrared reflection–absorption spectroscopy measurements
Polarization modulation-infrared reflection–absorption spectroscopy (PM-IRRAS) (Bruker, Germany) experiments were conducted to detect the change in organic films at the air–aqueous interface in both dark and irradiation conditions. IRRAS spectra of organic film are generally presented as plots of reflectance–absorbance against wavenumber. Reflectance–absorbance is defined as , where R is the reflectivity of the film-covered surface and Ro is the reflectivity of the aqueous subphase. The incident beam is directed onto the aqueous solution surface in the Langmuir trough at a 40∘ angle based on our previous study (Li et al., 2017b). Then, the reflected beam is measured by the MCT detector. The polarization modulation can modulate incident light into p polarization (perpendicular to the reflection plane) and s polarization (parallel to the reflection plane). The difference between the s-polarized and p-polarized spectra can provide information on the organic films at the air–aqueous interface. The spectra were recorded at both polarizations simultaneously due to the high scanning frequency of 42 kHz, thus eliminating the effects of the water vapour and carbon dioxide. When the surface pressure of the organic monolayer reached the set value of 25 mN m−1, the IRRAS spectra were recorded in the range of 400–4000 cm−1. Each spectrum averaged 2000 scans and had a resolution of 8 cm−1. The variability in the IRRAS peaks over the three trials was smaller than 2 cm−1, as shown in Fig. S3. In the irradiation experiment, first the black lamp was turned on at the surface pressure of 25 mN m−1, starting irradiation. IRRAS spectra were measured when 1.5 h irradiation was finished. The experiments in the absence of irradiation were performed to guarantee that the shifts of band position are induced by photochemical oxidation and are not related to spectra variability. Figure 1b shows a schematic of the IRRAS and irradiation setups.
3.1 Packing and phase behaviour of lipid monolayers
The monolayers usually composed of amphiphilic molecules with a hydrophilic head and a hydrophobic tail are assembled vertically at the air–water interface. Surface pressure–area (π–A) isotherms show phase transition behaviours of organic films. Owing to the amphiphilic characteristics of phospholipids, the head groups of DOPC and DSPC molecules prefer to be in the solution, while their tails stretch into the air. The π–A isotherms recorded for the DOPC and DSPC monolayers on artificial seawater with and without photosensitizers are shown in Fig. 2a and b, respectively. When the surface area of the DOPC monolayer was larger than 125 Å2/molecule, the distance between the DOPC molecules was quite large and the intermolecular force was quite weak. The surface pressure of a DOPC monolayer on artificial seawater started to increase from 125 Å2/molecule, where the DOPC monolayer surface state underwent a transition from the gas to the liquid-condensed phase. After the first phase transition, there is a proportional increase in surface pressure with decreasing area. This caused condensation and ordering at the interface, increasing the surface pressure of the organic monolayer. This trend continued up to a point where the DOPC molecules were packed closely and have very little space to move. Finally, the DOPC monolayer collapsed at 46 mN m−1 (Pereira et al., 2018). Applying an increasing pressure at the collapse pressure caused the monolayer to become unstable and destroy the monolayer. The packing and phase behaviours of the DOPC monolayer at different pressures are also shown in the inserts in Fig. 2a.
The π–A isotherms of the DOPC monolayers were shifted to larger molecular areas upon the introduction of the photosensitizing molecules into the bulk artificial seawater. Due to their high water solubility, pure IC and HA molecules cannot form Langmuir monolayers. The collapse pressure of the DOPC monolayer on pure artificial seawater decreased from 46 to 28 mN m−1 with the addition of 2.5 mM IC. The collapse pressure for the DOPC monolayer on the artificial seawater containing 30 mg L−1 HA was even lower. The DOPC monolayers on the artificial seawater containing water-soluble organic species extracted from PM2.5 and SOA samples also shifted to larger areas. The collapse pressure for the DOPC monolayer on the artificial seawater with the PM2.5 sample was 41 mN m−1. The π–A isotherms of the DOPC monolayer on artificial seawater mixed with the SOA sample and IC overlaps in the liquid-condensed phase. Finally, the curve of the DOPC monolayer on artificial seawater containing the SOA sample showed a collapse pressure similar to that on pure artificial seawater. In contrast to IC and HA, the collapse pressures of the DOPC monolayer were higher in the PM2.5 and SOA samples. The inorganic ions from the PM2.5 and SOA samples, like metal ions, may contribute to the organization of the organic monolayer (Adams et al., 2016, 2017; Denton et al., 2019).
In line with previous studies, DSPC molecules pack closely and form numerous van der Waals bonds to hold the DSPC monolayer together, with a collapse pressure of 55 mN m−1 (Chou et al., 2002; Yin et al., 2016). The appearance of the secondary increase in surface pressure after the DSPC monolayer collapsed indicated that the DSPC monolayer had a tendency to form a multiple layer. The lift-off area is the area where the surface pressure of the organic monolayer starts to increase. Although the structures of DSPC and DOPC are quite similar, the lift-off area for the DSPC monolayer on artificial seawater was smaller than that for the DOPC monolayer in Fig. 2b. The difference in the lift-off areas can be attributed to the unsaturated aliphatic chains in the DOPC molecule, which induce a less ordered structure relative to DSPC with saturated chains. The less tight packing of the hydrocarbon tail in DOPC could create more space for the incorporation of photosensitizer molecules, which is in good agreement with the earlier report (Aoki et al., 2016). The introduction of HA into the subphase also had a profound effect on the shape of π–A isotherms for DSPC monolayers. At any fixed surface pressure, the molecular area for the DSPC monolayer on artificial seawater with HA was much larger than that for just the DSPC monolayer.
As shown in Fig. 3, the lift-off area for the SA monolayer is 40 Å2/molecule, which is substantially smaller than the lift-off areas for the EA and OA monolayers. Completely saturated stearic acid has a straight chain which can pack tightly into an untilted-condensed (UC) phase. The surface pressure of EA and OA monolayers began increasing at the same molecular area of 82 Å2/molecule. The unsaturation in the alkyl chains of EA and OA is responsible for the differences in the lift-off areas. Compared to a fully saturated SA with the same number of carbon atoms, elaidic acid and oleic acid molecules possessing a double bond cannot be fully condensed into a monolayer. However, the EA monolayer can reach a maximum surface pressure of 34 mN m−1, which is higher than that of OA (below 20 mN m−1). Elaidic acid has a double bond at the number 9 carbon. The double bond of the alkane chain in elaidic acid is trans; therefore, the elaidic acid molecule remains straight and can still pack well in a monolayer (Kanicky and Shah, 2002). Oleic acid is the cis isomer of elaidic acid. The kink and bend of the alkyl chain at the position of the cis double bond induced steric hindrance during the compression of oleic acid molecules. The oleic acid monolayer was less able to pack as tightly as elaidic acid and form a tilted-condensed (TC) phase.
In the presence of IC in the artificial seawater, the fatty acid monolayers shifted to smaller areas and had higher collapse pressures relative to pure artificial seawater. The lift-off area value of 60 Å2/molecule for the EA monolayer on artificial seawater containing IC is larger compared to the saturated SA monolayer on the same subphase (28 Å2/molecule). The EA monolayers on the artificial seawater containing IC transitioned from TC to UC phase at the surface pressure of about 7–8 mN m−1 during the monolayer formation. Additionally, the EA monolayer exhibits the TC and UC phase transition below 17 ∘C (Iimura et al., 2001). The EA monolayer on the artificial seawater containing IC collapsed at the surface pressure of 46 mN m−1. The collapse of the OA monolayer on the artificial seawater containing IC occurred in the TC state at a surface pressure of 24 mN m−1. The behaviour in the UC phase of the EA monolayer is similar to that of the SA monolayer, reflecting that the photosensitizer molecules may be squeezed out of the tail of EA at high surface pressure. There is a remarkable obstructive effect on the ordering of organic film for the film-forming molecule that contains a cis double bond. The cis double bond in OA disturbs close packing of the molecules and weakens the chain–chain attractive interaction (Iimura et al., 2001). Therefore, OA has a greater tendency to form expanded monolayers.
3.2 Stability of lipid monolayers under irradiation
In order to get a better understanding of stability behaviour and the relaxation mechanism for lipid monolayers at the air–water interface, we measured area relaxation curves at a fixed surface pressure of 25 mN m−1 for both the dark and irradiated experiments. The change in relative area (A∕A0) for the lipid monolayer was analysed as a function of time. A0 represents the initial area for the DOPC monolayer at the surface pressure of 25 mN m−1. The relative area curves of the irradiated and non-irradiated DOPC monolayers are shown in Fig. 4a–e. The curve for the DOPC monolayer on pure artificial seawater exposed to the illumination was similar to that without irradiation. However, considerable changes in molecular areas for the DOPC monolayer were observed when the irradiation started in the presence of a photosensitizer. The relative area of the DOPC monolayer on pure artificial seawater was reduced to 30 % after 90 min irradiation. It is evident that the presence of photosensitizing molecules in the subphases decreased the loss of the molecular area for the DOPC monolayer. In the case of artificial seawater containing IC and HA (Fig. 4b–c), the molecular area of the DOPC monolayer after 90 min of irradiation was reduced to 89 % and 74 %, respectively. The loss of molecular area for the DOPC monolayer on the artificial seawater containing the SOA sample was similar to that in artificial seawater containing HA. In the presence of artificial seawater mixed with the PM2.5 samples, there was only a 5 % loss of the molecular area of the DOPC monolayer after 90 min of irradiation. The results of these curves indicated that there was no photosensitized reaction with only artificial seawater solutions. The decreasing trend of the molecular area for the irradiated DOPC monolayer on artificial seawater was due to the loss of organic molecules in the subphase. The rapid loss of molecular area on pure artificial seawater was related to spontaneous lipid degradation by oxidation, which was induced by reactive oxygen species in the air (Liljeblad et al., 2010).
In the presence of photosensitizers, the relative areas of the irradiated DOPC monolayers became larger than those of the non-irradiated DOPC as summarized in Fig. 4f. It is clearly shown where the effect of the photosensitizer on both the DOPC monolayer in the dark and irradiation is illustrated as a relative increase in area (Δ). The presence of IC and HA in the subphase yielded relative area increases (Δ) of 51 % and 50 % for the DOPC monolayer, respectively. The similar increase in relative area was also observed in the presence of SOA or the PM2.5 sample. The relative increases in molecular area for the DOPC monolayer mixed with the SOA sample were 43 %. The relative area increase for the DOPC monolayer with the PM2.5 sample after 90 min of irradiation reached 41 %. The area loss observed for lipid monolayers for the different compositions of the subphases, at a constant surface pressure, is indicative of their stability (Avila et al., 1999). Compared to the experiments without irradiation, DOPC monolayers were considerably more stable upon irradiation with a photosensitizer. The results of relative area suggested that photosensitizers induce possible reactions of DOPC under irradiation.
There were no significant changes in the molecular areas for the DSPC monolayers with and without exposure to light (Figs. S4–S6). In the irradiation experiments, the decrease in the DSPC monolayer area in artificial seawater with IC and HA is less than 5 % after 90 min. The loss of the DSPC monolayer area after 90 min of irradiation is at least 13 % with respect to the subphase of pure artificial seawater without photosensitizers. In irradiation experiments, the relative areas of the DSPC monolayer on the artificial seawater mixed with IC or HA were much closer to those experiments without irradiation. Therefore, the stability of the DSPC monolayer on the artificial seawater containing photosensitizers did not change much between the irradiated and dark experiments. DSPC monolayers are typically more stable than DOPC ones, irrespective of irradiation. The smaller loss of molecular area suggested that the presence of photosensitizer molecules in the subphase improved the stability of the lipid monolayer relative to pure artificial seawater. The different results of the relative area curve between the DOPC and DSPC monolayers implied that different reactions were induced by photosensitizers under irradiation.
3.3 Ordering of lipid monolayers at the air–aqueous interface with or without irradiation
The molecular-level interactions of photosensitizers with DOPC and DSPC monolayers can be analysed by surface-sensitive PM-IRRAS. In the dark experiment on pure artificial seawater (Fig. 5a) the bands at 2922 and 2853 cm−1 were assigned to antisymmetric (νas(CH2)) and symmetric methylene (-CH2-) stretching (νs(CH2)) modes, respectively. The antisymmetric (νas(CH3)) and symmetric methyl stretching (νs(CH3)) vibrations were observed at 2959 and 2882 cm−1, respectively. The observation of the CH3 bands indicated the gauche defects in the alkyl chain (Li et al., 2017a). The CH stretching in the HC=CH group at 3023 cm−1 was relatively weak. In the absence of photosensitizers, there were no significant changes in the IRRAS spectra for the DOPC monolayer after 90 min of irradiation. For the DOPC monolayer on the artificial seawater containing IC molecules, the bands of νas(CH2) and νs(CH2) stretching were observed at 2923 and 2854 cm−1, respectively. After 90 min of irradiation, the νas(CH2) and νs(CH2) bands were shifted to lower wavenumbers at 2921 and 2842 cm−1, respectively. The shifts in the CH2 and CH3 bands to lower wavenumbers indicate that the gauche rotamers in the DOPC monolayer were decreased after 90 min of irradiation. Therefore, the conformation order of the aliphatic chains in the DOPC monolayer was increased. According to Fig. 5e, the shifts in these CH2 and CH3 bands induced by IC were the most dramatic among the four samples in the photosensitized reaction of the organic aerosol surface. The peak height intensity ratio between the antisymmetric CH2 stretching (Ias) and symmetric CH2 stretching (Is) is usually used to assess the order of the organic monolayer packing (Aoki et al., 2016; Huang et al., 1982). In the case of IC in the subphase, the peak height intensity ratio between Ias and Is in the DOPC monolayer increased from 1.61 to 1.82 due to irradiation. The increase in the peak height ratio also occurred in the presence of HA. It indicated the order of the monolayer chains was increased. With respect to DOPC mixed with the PM2.5 sample (Fig. 5b), the ratio between Ias and Is increased from 1.48 to 1.73 under irradiation. The band of ν(HC=CH) at 3023 cm−1 was shifted to 3020 cm−1 under the irradiation of the DOPC monolayer mixed with IC. It indicated that the aliphatic chains became more ordered under irradiation. The existence of the ν(HC=CH) band in the irradiation experiment suggested that the aliphatic chain of DOPC molecules does not break at the initial position of the double bond. The new weak bands at 3001, 3007, and 3009 cm−1 that appeared after irradiation were also assigned to ν(HC=CH) stretching. This band implied the formation of unsaturated products in the photosensitized reaction.
The antisymmetric P=O stretching (νas()) band and the symmetric stretching (νs()) band for the DOPC monolayer on pure artificial seawater (Fig. 5c) were located at 1227 and 1073 cm−1, respectively. The bands of asymmetric carbonyl ester stretching (νas(CO–O–C)) at 1187 cm−1 shifted to 1161 and 1167 cm−1 for the DOPC monolayer mixed with IC and HA, respectively. For the DOPC monolayer on the artificial seawater containing the SOA sample, the νas() band at 1236 cm−1 and the νs() band at 1084 cm−1 (Fig. 5d) were shifted to 1231 and 1062 cm−1, respectively. The shifts in the P=O stretching vibrations suggested that hydrogen bonding between phosphate groups and surrounding water molecules appeared to be affected by irradiation. The band at 1059 cm−1 assigned to νs(C–O–) vibration was shifted to 1070 cm−1 for the DOPC monolayer on the artificial seawater containing the PM2.5 sample. These shifts in phosphate bands indicated that the interaction between photosensitizer and DOPC molecules induced the dehydration of phosphate groups (Arrondo et al., 1984). In the presence of the SOA sample in the subphase, the antisymmetric stretching of the choline group νas(CN+(CH3)3) band of the irradiated DOPC monolayer was shifted from 967 to 942 cm−1, which indicated that photosensitizer molecules affected the hydration of DOPC head groups.
The spectral shifts induced by the photosensitizer and irradiation were more obvious for the DOPC monolayers than for the DSPC ones. With respect to the DSPC monolayer on the artificial seawater, the antisymmetric CH2 stretching and symmetric CH2 stretching (Fig. S7a) were 2919 and 2851 cm−1, respectively. The CH2 bands in the DSPC monolayers were more intense relative to the DOPC monolayer, thus shifting to lower wavenumbers. This can be attributed to the formation of a more compressed and packed DSPC monolayer relative to DOPC. Lower wavenumbers of CH2 bands are indicative of highly ordered conformation with all-trans characteristics (Simon-Kutscher et al., 1996; Christoforou et al., 2012; Snyder et al., 1978). Minimal wavenumber shifts of P=O, C–O–, and CN+(CH3)3 stretching vibrations were observed under irradiation in Fig. S7b. According to the comparison with the IRRAS spectra of the DSPC monolayer in dark conditions, no new bands of products were observed from the irradiated DSPC film. This result suggested that the DSPC films were less affected by irradiation.
3.4 Proposed mechanism for photosensitized reaction of lipid monolayers at the air–aqueous interface
These light-absorbing organic aerosol species can participate in the aging of organic aerosol by acting as photosensitizers. Upon light activation, the excited triplet state of the photosensitizer can undergo type I (electron transfer) and/or type II (energy transfer) reactions to generate a variety of highly reactive oxygen species (ROS) (Ding et al., 2011; Aguer et al., 1999). A type I reaction can reduce molecular oxygen (O2), generating oxidizing radicals and radical anion species (e.g. O2•−, HO•), while a type II reaction can transfer energy to O2 to produce singlet oxygen (1O2). The triplet excited state of IC (3IC*), HA (3HA*), and HULIS (3HULIS*) also can directly oxidize other organic material (Tsui et al., 2017; Tsui and McNeill, 2018; Shrestha et al., 2018).
These ROS, along with the triplet excited state of photosensitizers, can react with lipids at the air–aqueous interface, resulting in the photochemical aging of organic film on the aqueous aerosol surface. The slow oxidation of DSPC molecules at the air–seawater interface in the ambient environment does not produce sufficient surface-active molecules, leading to the loss of DSPC molecules from the surface. Previous irradiation studies suggest that green light (530 nm) induced little loss in the surface area of the saturated 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) monolayer mixed with photosensitive erythrosine or eosin Y molecules (Pereira et al., 2018; Aoki et al., 2016). When considering the liposomal binary mixture of phospholipids containing 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (DC8,9PC) and DPPC, DC8,9PC can produce intermolecular cross-linking following the release of 5,6-carboxyfluorescein dye under UV irradiation. The same photochemical reaction had no effect on DPPC molecules, even when exposed to radiation with a wavelength of 254 nm, which carries relatively greater energy (Kenaan et al., 2018). Both DSPC and DPPC molecules possess the same phosphocholine head and saturated aliphatic chain, which is likely why there is rather similar activity of DPPC and DSPC with the photosensitizer under irradiation. We inferred that the photo-induced reaction did not occur for the DSPC monolayer based on the relative area relaxation curves and IRRAS results of the DSPC monolayer.
Unsaturated lipids are more susceptible to the attack of 1O2 and free radicals. Reactions of 1O2 with unsaturated bonds in lipid chains can generate hydroperoxide (OOH) groups and then increase the molecular area of a lipid monolayer due to hydrophilic–hydrophobic balance of the modified chain (Caetano et al., 2007; Riske et al., 2009; Aoki et al., 2016; Pereira et al., 2018). The new band corresponding to CH stretching vibration of the HC=CH group was measured by IRRAS, while other bands were changed little in Fig. 5. We infer that the structure of the photochemical product is similar to DOPC. According to the mechanism of the photosensitizing reaction, the unsaturated product detected by IRRAS is possible to be DOPC hydroperoxide. The hydroperoxide group in DOPC is more water-soluble than the aliphatic chain of DOPC (Fig. 6a). Moreover, DOPC hydroperoxides may further transport toward the hydrophilic region of the monolayer and dissolve into the aqueous phase, leading to a larger surface area of the DOPC monolayer at the air–aqueous interface (Brault et al., 1986). In contrast to a pure DOPC monolayer, the formation of hydroperoxides produced by hydroperoxidation reaction between 1O2 and DOPC can be considered the reason for the distinct relative area increase (Δ) in Fig. 4c. Giant unilamellar vesicles containing a large amount of unsaturated lipids exhibited a rapid increase in surface area, resulting in morphological changes under irradiation (Riske et al., 2009). Simulations of molecular dynamics also showed that the hydroperoxide group of lipids has a tendency to reside close to the surface with a concomitant expansion of surface area per molecule (Neto and Cordeiro, 2016; Wong-Ekkabut et al., 2007). The PM-IRRAS technique had no response at the OOH band; therefore, we did not directly detect DOPC hydroperoxides by IRRAS. The new bands of ν(HC=CH) at 3001, 3007, and 3009 cm−1 also support the formation of unsaturated DOPC hydroperoxides present at the air–aqueous interface. The mechanism for the photochemical reaction of the DOPC monolayer by the excited photosensitizer is summarized in Fig. 6b. Lipid hydroperoxides are the primary oxidation products and are relatively stable at room temperature. After the initiation phase of hydroperoxide formation, lipid hydroperoxides may further decompose to radicals, leading to the formation of ketones, aldehydes, carboxylic acids, alcohols, esters, and short-chain hydrocarbons (Ghnimi et al., 2017; Choe and Min, 2006). Free radical chain reactions increased the formation of secondary oxidation products. The unsaturated fatty acids also followed this mechanism during the processing of photosensitized oxidation.
Past research has proposed the mechanism for the photosensitized degradation of a saturated fatty acid by the excited photosensitizer at the air–water interface (Tinel et al., 2016; Shrestha et al., 2018; Alpert et al., 2017). The radical produced by the initial hydrogen abstraction of the fatty acid can undergo two possible pathways. In the first pathway, the radical–radical reactions were favoured in an oxygen-poor environment. In the second pathway, in an oxygen-rich environment, the reaction between fatty acid radicals and molecular oxygen can produce peroxy radicals which can further decompose to saturated ketones or other oxidized compounds with hydroxyl and carbonyl functional groups. Then, these compounds can continue to react with molecular oxygen and the excited state of the photosensitizer to produce fatty acid radicals and more highly oxidized species.
3.5 Atmospheric implication
In this work, photosensitizers like IC and HA in the aqueous core of aerosol can take part in the oxidation of unsaturated lipid film coated on the aerosol in the presence of UV light. There was significant organic aerosol aging. The results such as relative area increase and new IRRAS bands of the unsaturated products also indicate that chamber-generated SOA samples and authentic PM2.5 samples were involved in the photosensitizing reaction of the DOPC monolayer. The introduction of an authentic PM2.5 sample in this simulated experiment suggested that such a process of organic aerosol aging may be occurred in the atmosphere.
The hydrophobic characteristics of organic film were changed greatly in the process of organic aerosol aging. According to the mechanism of photosensitizing reaction, the possible products, DOPC hydroperoxides, were more water-soluble. They appear to dissolve into bulk artificial seawater and partition into the hydrophilic core of organic aqueous aerosols. Subsequently, the processes of hygroscopic growth of aerosol and cloud condensation nuclei activation are impacted. If the organic film on the aerosol surface is either destabilized under irradiation or it is metastable due to the loss of ordering and packing, the organic aerosol will become more permeable to water. As a result, the hygroscopicity of the aerosol particle and the overall size of the droplet can increase (Ruehl and Wilson, 2014). Consequently, the atmospheric lifetime of unsaturated species on the aerosol surface can decrease. Volatility is generally inversely correlated with the O:C ratio (Aiken et al., 2008). The photochemical reaction at the air–aqueous interface under the condition of BrC is an efficient and common pathway to oxidize organic films toward low volatile organic compounds (O:C ratio of 0.25 to 1) (Jimenez et al., 2009). Moreover, the photosensitized reaction of organic aqueous aerosol likely depends on the film-forming species, given the different reactivities of saturated and unsaturated phospholipids.
We have investigated the photosensitized reactions of saturated and unsaturated organic monolayers at the air–water interface as proxies for the photochemical aging of organic-coated aqueous aerosols by BrC. The surfactant molecules SA, EA, OA, DSPC, and DOPC were chosen to investigate the effects of degree of unsaturation and conformation on the ordering, packing, and stability of organic film. The surface areas of the unsaturated lipids (EA, OA, and DOPC) with the double bond in the 9 position were much more expanded than the saturated conformations with the same chain lengths. The types of configurational isomers (cis and trans) affected the surface properties of the organic monolayer. The π–A isotherms suggested that the EA monolayer had a slightly higher compressibility than the OA monolayer. According to relative area increase curves, the addition of photosensitizers into the subphase increased the stability of DSPC and DOPC monolayers on the aerosol surface, irrespective of irradiation or non-irradiation. The saturated DSPC monolayer has greater photochemical stability than the DOPC monolayer. The relative areas of DOPC monolayers in the artificial seawater containing photosensitizers were increased after irradiation. In addition, the largest increase in the relative area of the DOPC monolayer was observed in the presence of IC, as compared to the laboratory-generated SOA sample and field-collected PM2.5 sample. The changes between the irradiated and dark PM-IRRAS spectra also support the photochemical oxidation of the unsaturated chains in DOPC. DOPC hydroperoxides were considered to be primary oxidation products during the photochemical oxidation of unsaturated lipids via singlet oxygen generation. The photosensitized reaction of DOPC monolayers at the surface of aqueous aerosol can lead to the formation of more oxidized and therefore less reactive species at the surface. Overall, the transformation of hydrophobic organic materials into hydrophilic organic components can alter the hygroscopicity of an organic aerosol particle.
Data are available by contacting the corresponding author.
The supplement related to this article is available online at: https://doi.org/10.5194/acp-19-9887-2019-supplement.
LD and SL conceived and led the studies. SL, XJ, and LL carried out the experiments and analysed the data. SL, LD, CG, and MR interpreted the results. WJ, QZ, WW, and MG discussed the results and commented on the manuscript. SL prepared the manuscript with contributions from all the co-authors.
The authors declare that they have no conflict of interest.
This article is part of the special issue “Multiphase chemistry of secondary aerosol formation under severe haze”. It is not associated with a conference.
This research has been supported by the National Natural Science Foundation of China (grant nos. 91644214 and 21876098), the Shandong Natural Science Fund for Distinguished Young Scholars (grant no. JQ201705), the Shandong Key R&D Program (grant no. 2018GSF117040), the Fundamental Research Funds of Shandong University (grant no. 2017JQ01), the Taishan Scholars (grant no. ts201712003), and the Marie Curie International Research Staff Exchange project MARSU (grant no. 690958).
This paper was edited by Daniel Knopf and reviewed by three anonymous referees.
Ackendorf, J. M., Ippolito, M. G., and Galloway, M. M.: pH Dependence of the Imidazole-2-carboxaldehyde Hydration Equilibrium: Implications for Atmospheric Light Absorbance, Environ. Sci. Tech. Let., 4, 551–555, https://doi.org/10.1021/acs.estlett.7b00486, 2017.
Adams, E. M., Verreault, D., Jayarathne, T., Cochran, R. E., Stone, E. A., and Allen, H. C.: Surface organization of a DPPC monolayer on concentrated SrCl2 and ZnCl2 solutions, Phys. Chem. Chem. Phys., 18, 32345–32357, https://doi.org/10.1039/c6cp06887a, 2016.
Adams, E. M., Wellen, B. A., Thiraux, R., Reddy, S. K., Vidalis, A. S., Paesani, F., and Allen, H. C.: Sodium-carboxylate contact ion pair formation induces stabilization of palmitic acid monolayers at high pH, Phys. Chem. Chem. Phys., 19, 10481–10490, https://doi.org/10.1039/c7cp00167c, 2017.
Aguer, J. P., Richard, C., and Andreux, F.: Effect of light on humic substances: Production of reactive species, Analusis, 27, 387–390, https://doi.org/10.1051/analusis:1999270387, 1999.
Aiken, A. C., Decarlo, P. F., Kroll, J. H., Worsnop, D. R., Huffman, J. A., Docherty, K. S., Ulbrich, I. M., Mohr, C., Kimmel, J. R., Sueper, D., Sun, Y., Zhang, Q., Trimborn, A., Northway, M., Ziemann, P. J., Canagaratna, M. R., Onasch, T. B., Alfarra, M. R., Prevot, A. S. H., Dommen, J., Duplissy, J., Metzger, A., Baltensperger, U., and Jimenez, J. L.: O∕C and OM∕OC ratios of primary, secondary, and ambient organic aerosols with high-resolution time-of-flight aerosol mass spectrometry, Environ. Sci. Technol., 42, 4478–4485, https://doi.org/10.1021/es703009q, 2008.
Aiona, P. K., Lee, H. J., Leslie, R., Lin, P., Laskin, A., Laskin, J., and Nizkorodov, S. A.: Photochemistry of Products of the Aqueous Reaction of Methylglyoxal with Ammonium Sulfate, ACS Earth Space Chem., 1, 522–532, https://doi.org/10.1021/acsearthspacechem.7b00075, 2017.
Alpert, P. A., Ciuraru, R., Rossignol, S., Passananti, M., Tinel, L., Perrier, S., Dupart, Y., Steimer, S. S., Ammann, M., Donaldson, D. J., and George, C.: Fatty Acid Surfactant Photochemistry Results in New Particle Formation, Sci. Rep.-UK, 7, 12693, https://doi.org/10.1038/s41598-017-12601-2, 2017.
Andreae, M. O. and Gelencsér, A.: Black carbon or brown carbon? The nature of light-absorbing carbonaceous aerosols, Atmos. Chem. Phys., 6, 3131–3148, https://doi.org/10.5194/acp-6-3131-2006, 2006.
Aoki, P. H. B., Morato, L. F. C., Pavinatto, F. J., Nobre, T. M., Constantino, C. J. L., and Oliveira, O. N.: Molecular-Level Modifications Induced by Photo-Oxidation of Lipid Monolayers Interacting with Erythrosin, Langmuir, 32, 3766–3773, https://doi.org/10.1021/acs.langmuir.6b00693, 2016.
Aregahegn, K. Z., Noziere, B., and George, C.: Organic aerosol formation photo-enhanced by the formation of secondary photosensitizers in aerosols, Faraday Discuss., 165, 123–134, https://doi.org/10.1039/c3fd00044c, 2013.
Arrondo, J. L. R., Goni, F. M., and Macarulla, J. M.: Infrared spectroscopy of phosphatidylcholines in aqueous suspension a study of the phosphate group vibrations, Biochim. Biophys. Acta, 794, 165–168, https://doi.org/10.1016/0005-2760(84)90310-2, 1984.
Arroyo, P. C., Bartels-Rausch, T., Alpert, P. A., Dumas, S., Perrier, S., George, C., and Ammann, M.: Particle-Phase Photosensitized Radical Production and Aerosol Aging, Environ. Sci. Technol., 52, 7680–7688, https://doi.org/10.1021/acs.est.8b00329, 2018.
Aumann, E., Hildemann, L. M., and Tabazadeh, A.: Measuring and modeling the composition and temperature-dependence of surface tension for organic solutions, Atmos. Environ., 44, 329–337, https://doi.org/10.1016/j.atmosenv.2009.10.033, 2010.
Avila, L. V. N., Saraiva, S. M., and Oliveira, J. F.: Stability and collapse of monolayers of stearic acid and the effect of electrolytes in the subphase, Colloid Surface A, 154, 209–217, https://doi.org/10.1016/s0927-7757(98)00899-1, 1999.
Berke, A. E., Bhat, T. A., Myers, H., Gubbins, E. F., Nwankwo, A. A. O., Lu, K., Timpane, L., and Keller, C.: Effect of short-chain alcohols on the bulk-phase reaction between glyoxal and ammonium sulfate, Atmos. Environ., 198, 407–416, https://doi.org/10.1016/j.atmosenv.2018.11.015, 2019.
Bernard, F., Ciuraru, R., Boreave, A., and George, C.: Photosensitized Formation of Secondary Organic Aerosols above the Air/Water Interface, Environ. Sci. Technol., 50, 8678–8686, https://doi.org/10.1021/acs.est.6b03520, 2016.
Bertram, T. H., Cochran, R. E., Grassian, V. H., and Stone, E. A.: Sea spray aerosol chemical composition: elemental and molecular mimics for laboratory studies of heterogeneous and multiphase reactions, Chem. Soc. Rev., 47, 2374–2400, https://doi.org/10.1039/c7cs00008a, 2018.
Bones, D. L., Henricksen, D. K., Mang, S. A., Gonsior, M., Bateman, A. P., Nguyen, T. B., Cooper, W. J., and Nizkorodov, S. A.: Appearance of strong absorbers and fluorophores in limonene-O3 secondary organic aerosol due to -mediated chemical aging over long time scales, J. Geophys. Res.-Atmos., 115, D05203, https://doi.org/10.1029/2009jd012864, 2010.
Brault, D., Veverbizet, C., and Ledoan, T.: Spectrofluorimetric study of porphyrin incorporation into membrane models – evidence for pH effects, Biochim. Biophys. Acta, 857, 238–250, https://doi.org/10.1016/0005-2736(86)90352-4, 1986.
Bruggemann, M., Hayeck, N., Bonnineau, C., Pesce, S., Alpert, P. A., Perrier, S., Zuth, C., Hoffmann, T., Chen, J. M., and George, C.: Interfacial photochemistry of biogenic surfactants: a major source of abiotic volatile organic compounds, Faraday Discuss., 200, 59–74, https://doi.org/10.1039/c7fd00022g, 2017.
Brzozowska, A. M., Duits, M. H. G., and Mugele, F.: Stability of stearic acid monolayers on Artificial Sea Water, Colloid Surface A, 407, 38–48, https://doi.org/10.1016/j.colsurfa.2012.04.055, 2012.
Brzozowska, A. M., Mugele, F., and Duits, M. H. G.: Stability and interactions in mixed monolayers of fatty acid derivatives on Artificial Sea Water, Colloid Surface A, 433, 200–211, https://doi.org/10.1016/j.colsurfa.2013.04.062, 2013.
Caetano, W., Haddad, P. S., Itri, R., Severino, D., Vieira, V. C., Baptista, M. S., Schroder, A. P., and Marques, C. M.: Photo-induced destruction of giant vesicles in methylene blue solutions, Langmuir, 23, 1307–1314, https://doi.org/10.1021/la061510v, 2007.
Carpenter, L. J. and Nightingale, P. D.: Chemistry and Release of Gases from the Surface Ocean, Chem. Rev., 115, 4015–4034, https://doi.org/10.1021/cr5007123, 2015.
Cavalli, F., Facchini, M. C., Decesari, S., Mircea, M., Emblico, L., Fuzzi, S., Ceburnis, D., Yoon, Y. J., O'Dowd, C. D., Putaud, J. P., and Dell'Acqua, A.: Advances in characterization of size-resolved organic matter in marine aerosol over the North Atlantic, J. Geophys. Res.-Atmos., 109, D24215 https://doi.org/10.1029/2004jd005137, 2004.
Choe, E. and Min, D. B.: Mechanisms and factors for edible oil oxidation, Compr. Rev. Food. Sci. F., 5, 169–186, https://doi.org/10.1111/j.1541-4337.2006.00009.x, 2006.
Chou, T. H., Chu, I. M., and Chang, C. H.: Interaction of paclitaxel with DSPC in monolayers at the air/water interface at different temperatures, Colloid Surface B, 25, 147–155, https://doi.org/10.1016/s0927-7765(01)00303-4, 2002.
Christoforou, M., Leontidis, E., and Brezesinski, G.: Effects of Sodium Salts of Lyotropic Anions on Low-Temperature, Ordered Lipid Monolayers, J. Phys. Chem. B, 116, 14602–14612, https://doi.org/10.1021/jp307004e, 2012.
Collins, D. B., Bertram, T. H., Sultana, C. M., Lee, C., Axson, J. L., and Prather, K. A.: Phytoplankton blooms weakly influence the cloud forming ability of sea spray aerosol, Geophys. Res. Lett., 43, 9975–9983, https://doi.org/10.1002/2016gl069922, 2016.
Davies, J. F., Miles, R. E. H., Haddrell, A. E., and Reid, J. P.: Influence of organic films on the evaporation and condensation of water in aerosol, P. Natl. Acad. Sci. USA, 110, 8807–8812, https://doi.org/10.1073/pnas.1305277110, 2013.
Denton, J. K., Kelleher, P. J., Johnson, M. A., Baer, M. D., Kathmann, S. M., Mundy, C. J., Wellen Rudd, B. A., Allen, H. C., Choi, T. H., and Jordan, K. D.: Molecular-level origin of the carboxylate head group response to divalent metal ion complexation at the air-water interface, P. Natl. Acad. Sci. USA, 116, 14874–14888, https://doi.org/10.1073/pnas.1818600116, 2019.
Desyaterik, Y., Sun, Y., Shen, X., Lee, T., Wang, X., Wang, T., and Collett Jr., J. L.: Speciation of “brown” carbon in cloud water impacted by agricultural biomass burning in eastern China, J. Geophys. Res.-Atmos., 118, 7389–7399, https://doi.org/10.1002/jgrd.50561, 2013.
Ding, H. Y., Yu, H. J., Dong, Y., Tian, R. H., Huang, G., Boothman, D. A., Sumer, B. D., and Gao, J. M.: Photoactivation switch from type II to type I reactions by electron-rich micelles for improved photodynamic therapy of cancer cells under hypoxia, J. Control. Release, 156, 276–280, https://doi.org/10.1016/j.jconrel.2011.08.019, 2011.
Donaldson, D. J. and Vaida, V.: The influence of organic films at the air-aqueous boundary on atmospheric processes, Chem. Rev., 106, 1445–1461, https://doi.org/10.1021/cr040367c, 2006.
Donaldson, D. J. and Valsaraj, K. T.: Adsorption and Reaction of Trace Gas-Phase Organic Compounds on Atmospheric Water Film Surfaces: A Critical Review, Environ. Sci. Technol., 44, 865–873, https://doi.org/10.1021/es902720s, 2010.
Ellison, G. B., Tuck, A. F., and Vaida, V.: Atmospheric processing of organic aerosols, J. Geophys. Res.-Atmos., 104, 11633–11641, https://doi.org/10.1029/1999jd900073, 1999.
Emmenegger, C., Reinhardt, A., Hueglin, C., Zenobi, R., and Kalberer, M.: Evaporative light scattering: A novel detection method for the quantitative analysis of humic-like substances in aerosols, Environ. Sci. Technol., 41, 2473–2478, https://doi.org/10.1021/es061095t, 2007.
Feczko, T., Puxbaum, H., Kasper-Giebl, A., Handler, M., Limbeck, A., Gelencser, A., Pio, C., Preunkert, S., and Legrand, M.: Determination of water and alkaline extractable atmospheric humic-like substances with the TU Vienna HULIS analyzer in samples from six background sites in Europe, J. Geophys. Res.-Atmos., 112, D23S10, https://doi.org/10.1029/2006jd008331, 2007.
Flores, J. M., Washenfelder, R. A., Adler, G., Lee, H. J., Segev, L., Laskin, J., Laskin, A., Nizkorodov, S. A., Brown, S. S., and Rudich, Y.: Complex refractive indices in the near-ultraviolet spectral region of biogenic secondary organic aerosol aged with ammonia, Phys. Chem. Chem. Phys., 16, 10629–10642, https://doi.org/10.1039/c4cp01009d, 2014.
Gelencser, A., Hoffer, A., Krivacsy, Z., Kiss, G., Molnar, A., and Meszaros, E.: On the possible origin of humic matter in fine continental aerosol, J. Geophys. Res.-Atmos., 107, 4137, https://doi.org/10.1029/2001jd001299, 2002.
Gelencser, A., Hoffer, A., Kiss, G., Tombacz, E., Kurdi, R., and Bencze, L.: In-situ formation of light-absorbing organic matter in cloud water, J. Atmos. Chem., 45, 25–33, https://doi.org/10.1023/a:1024060428172, 2003.
George, C., Ammann, M., D'Anna, B., Donaldson, D. J., and Nizkorodov, S. A.: Heterogeneous Photochemistry in the Atmosphere, Chem. Rev., 115, 4218–4258, https://doi.org/10.1021/cr500648z, 2015.
Ghnimi, S., Budilarto, E., and Kamal-Eldin, A.: The New Paradigm for Lipid Oxidation and Insights to Microencapsulation of Omega-3 Fatty Acids, Compr. Rev. Food. Sci. F., 16, 1206–1218, https://doi.org/10.1111/1541-4337.12300, 2017.
Gill, P. S., Graedel, T. E., and Weschler, C. J.: Organic films on atmospheric aerosol particles, fog droplets, cloud droplets, raindrops, and snowflakes, Rev. Geophys., 21, 903–920, https://doi.org/10.1029/RG021i004p00903, 1983.
González Palacios, L., Corral Arroyo, P., Aregahegn, K. Z., Steimer, S. S., Bartels-Rausch, T., Nozière, B., George, C., Ammann, M., and Volkamer, R.: Heterogeneous photochemistry of imidazole-2-carboxaldehyde: HO2 radical formation and aerosol growth, Atmos. Chem. Phys., 16, 11823–11836, https://doi.org/10.5194/acp-16-11823-2016, 2016.
Graber, E. R. and Rudich, Y.: Atmospheric HULIS: How humic-like are they? A comprehensive and critical review, Atmos. Chem. Phys., 6, 729–753, https://doi.org/10.5194/acp-6-729-2006, 2006.
Guschina, I. A. and Harwood, J. L.: Lipids and lipid metabolism in eukaryotic algae, Prog. Lipid Res., 45, 160–186, https://doi.org/10.1016/j.plipres.2006.01.001, 2006.
Hu, Q. H., Xie, Z. Q., Wang, X. M., Kang, H., Zhang, Y. Q., Ding, X., and Zhang, P. F.: Monocarboxylic and dicarboxylic acids over oceans from the East China Sea to the Arctic Ocean: Roles of ocean emissions, continental input and secondary formation, Sci. Total Environ., 640, 284–292, https://doi.org/10.1016/j.scitotenv.2018.05.311, 2018.
Huang, C. H., Lapides, J. R., and Levin, I. W.: Phase-transition behavior of saturated, symmetric chain phospholipid bilayer dispersions determined by Raman spectroscopy: correlation between spectral and thermodynamic parameters, J. Am. Chem. Soc., 104, 5926–5930, 1982.
Hyvärinen, A. R., Lihavainen, H., Gaman, A., Vairila, L., Ojala, H., Kulmala, M., and Viisanen, Y.: Surface tensions and densities of oxalic, malonic, succinic, maleic, malic, and cis-pinonic acids, J. Chem. Eng. Data, 51, 255–260, https://doi.org/10.1021/je050366x, 2006.
Iimura, K., Yamauchi, Y., Tsuchiya, Y., and Kato, T.: Two-dimensional dendritic growth of condensed phase domains in spread monolayers of cis-unsaturated fatty acids, Langmuir, 17, 4602–4609, https://doi.org/10.1021/la010236w, 2001.
Jeffrey, L. M.: Lipids in sea water, J. Am. Oil Chem. Soc., 43, 211–214, https://doi.org/10.1007/bf02641089, 1966.
Jiang, H., Frie, A. L., Lavi, A., Chen, J. Y., Zhang, H., Bahreini, R., and Lin, Y.-H.: Brown Carbon Formation from Nighttime Chemistry of Unsaturated Heterocyclic Volatile Organic Compounds, Environ. Sci. Tech. Let., 6, 184–190, https://doi.org/10.1021/acs.estlett.9b00017, 2019.
Jimenez, J. L., Canagaratna, M. R., Donahue, N. M., Prevot, A. S. H., Zhang, Q., Kroll, J. H., DeCarlo, P. F., Allan, J. D., Coe, H., Ng, N. L., Aiken, A. C., Docherty, K. S., Ulbrich, I. M., Grieshop, A. P., Robinson, A. L., Duplissy, J., Smith, J. D., Wilson, K. R., Lanz, V. A., Hueglin, C., Sun, Y. L., Tian, J., Laaksonen, A., Raatikainen, T., Rautiainen, J., Vaattovaara, P., Ehn, M., Kulmala, M., Tomlinson, J. M., Collins, D. R., Cubison, M. J., Dunlea, E. J., Huffman, J. A., Onasch, T. B., Alfarra, M. R., Williams, P. I., Bower, K., Kondo, Y., Schneider, J., Drewnick, F., Borrmann, S., Weimer, S., Demerjian, K., Salcedo, D., Cottrell, L., Griffin, R., Takami, A., Miyoshi, T., Hatakeyama, S., Shimono, A., Sun, J. Y., Zhang, Y. M., Dzepina, K., Kimmel, J. R., Sueper, D., Jayne, J. T., Herndon, S. C., Trimborn, A. M., Williams, L. R., Wood, E. C., Middlebrook, A. M., Kolb, C. E., Baltensperger, U., and Worsnop, D. R.: Evolution of Organic Aerosols in the Atmosphere, Science, 326, 1525–1529, https://doi.org/10.1126/science.1180353, 2009.
Kang, M. J., Yang, F., Ren, H., Zhao, W. Y., Zhao, Y., Li, L. J., Yan, Y., Zhang, Y. J., Lai, S. C., Zhang, Y. Y., Yang, Y., Wang, Z. F., Sun, Y. L., and Fu, P. Q.: Influence of continental organic aerosols to the marine atmosphere over the East China Sea: Insights from lipids, PAHs and phthalates, Sci. Total Environ., 607, 339–350, https://doi.org/10.1016/j.scitotenv.2017.06.214, 2017.
Kanicky, J. R. and Shah, D. O.: Effect of degree, type, and position of unsaturation on the pKa of long-chain fatty acids, J. Colloid Interf. Sci., 256, 201–207, https://doi.org/10.1006/jcis.2001.8009, 2002.
Kenaan, A., Cheng, J., Qi, D., Chen, D., Cui, D., and Song, J.: Physicochemical Analysis of DPPC and Photopolymerizable Liposomal Binary Mixture for Spatiotemporal Drug Release, Anal. Chem., 90, 9487–9494, https://doi.org/10.1021/acs.analchem.8b02144, 2018.
King, M. D., Rennie, A. R., Thompson, K. C., Fisher, F. N., Dong, C. C., Thomas, R. K., Pfrang, C., and Hughes, A. V.: Oxidation of oleic acid at the air-water interface and its potential effects on cloud critical supersaturations, Phys. Chem. Chem. Phys., 11, 7699–7707, https://doi.org/10.1039/b906517b, 2009.
Kristensen, T. B., Du, L., Nguyen, Q. T., Nojgaard, J. K., Koch, C. B., Nielsen, O. F., Hallar, A. G., Lowenthal, D. H., Nekat, B., van Pinxteren, D., Herrmann, H., Glasius, M., Kjaergaard, H. G., and Bilde, M.: Chemical properties of HULIS from three different environments, J Atmos. Chem., 72, 65–80, https://doi.org/10.1007/s10874-015-9302-8, 2015.
Krivacsy, Z., Kiss, G., Ceburnis, D., Jennings, G., Maenhaut, W., Salma, I., and Shooter, D.: Study of water-soluble atmospheric humic matter in urban and marine environments, Atmos. Res., 87, 1–12, https://doi.org/10.1016/j.atmosres.2007.04.005, 2008.
Laskin, A., Laskin, J., and Nizkorodov, S. A.: Chemistry of Atmospheric Brown Carbon, Chem. Rev., 115, 4335–4382, https://doi.org/10.1021/cr5006167, 2015.
Lee, A. K. Y., Zhao, R., Li, R., Liggio, J., Li, S.-M., and Abbatt, J. P. D.: Formation of Light Absorbing Organo-Nitrogen Species from Evaporation of Droplets Containing Glyoxal and Ammonium Sulfate, Environ. Sci. Technol., 47, 12819–12826, https://doi.org/10.1021/es402687w, 2013.
Li, S., Du, L., and Wang, W.: Impact of anions on the surface organisation of lipid monolayers at the air-water interface, Environ. Chem., 14, 407–416, https://doi.org/10.1071/en17147, 2017a.
Li, S., Du, L., Wei, Z., and Wang, W.: Aqueous-phase aerosols on the air-water interface: Response of fatty acid Langmuir monolayers to atmospheric inorganic ions, Sci. Total Environ., 580, 1155–1161, https://doi.org/10.1016/j.scitotenv.2016.12.072, 2017b.
Li, S., Du, L., Zhang, Q., and Wang, W.: Stabilizing mixed fatty acid and phthalate ester monolayer on artificial seawater, Environ. Pollut., 242, 626–633, https://doi.org/10.1016/j.envpol.2018.07.043, 2018.
Li, S., Cheng, S., Du, L., and Wang, W.: Establishing a model organic film of low volatile compound mixture on aqueous aerosol surface, Atmos. Environ., 200, 15–23, https://doi.org/10.1016/j.atmosenv.2018.11.052, 2019.
Li, W. Y., Li, X., Jockusch, S., Wang, H., Xu, B. L., Wu, Y. J., Tsui, W. G., Dai, H. L., McNeill, V. F., and Rao, Y.: Photoactivated Production of Secondary Organic Species from Isoprene in Aqueous Systems, J. Phys. Chem. A, 120, 9042–9048, https://doi.org/10.1021/acs.jpca.6b07932, 2016.
Li-Beisson, Y., Thelen, J. J., Fedosejevs, E., and Harwood, J. L.: The lipid biochemistry of eukaryotic algae, Prog. Lipid Res., 74, 31–68, https://doi.org/10.1016/j.plipres.2019.01.003, 2019.
Liljeblad, J. F. D., Bulone, V., Tyrode, E., Rutland, M. W., and Johnson, C. M.: Phospholipid Monolayers Probed by Vibrational Sum Frequency Spectroscopy: Instability of Unsaturated Phospholipids, Biophys. J., 98, L50–L52, https://doi.org/10.1016/j.bpj.2010.02.009, 2010.
Liu, S. J., Jiang, X. T., Tsona, N. T., Lv, C., and Du, L.: Effects of NOx, SO2 and RH on the SOA formation from cyclohexene photooxidation, Chemosphere, 216, 794–804, https://doi.org/10.1016/j.chemosphere.2018.10.180, 2019.
Malecha, K. T. and Nizkorodov, S. A.: Feasibility of Photosensitized Reactions with Secondary Organic Aerosol Particles in the Presence of Volatile Organic Compounds, J. Phys. Chem. A, 121, 4961–4967, https://doi.org/10.1021/acs.jpca.7b04066, 2017.
Marty, J. C., Saliot, A., Buatmenard, P., Chesselet, R., and Hunter, K. A.: Relationship between the lipid compositions of marine aerosols, the sea surface microlayer, and subsurface water, J. Geophys. Res.-Oceans, 84, 5707–5716, https://doi.org/10.1029/JC084iC09p05707, 1979.
McCarthy, M., Hedges, J., and Benner, R.: Major biochemical composition of dissolved high molecular weight organic matter in seawater, Mar. Chem., 55, 281–297, https://doi.org/10.1016/s0304-4203(96)00041-2, 1996.
Nakayama, T., Sato, K., Matsumi, Y., Imamura, T., Yamazaki, A., and Uchiyama, A.: Wavelength and NOx dependent complex refractive index of SOAs generated from the photooxidation of toluene, Atmos. Chem. Phys., 13, 531–545, https://doi.org/10.5194/acp-13-531-2013, 2013.
Neto, A. J. P. and Cordeiro, R. M.: Molecular simulations of the effects of phospholipid and cholesterol peroxidation on lipid membrane properties, BBA-Biomembranes, 1858, 2191–2198, https://doi.org/10.1016/j.bbamem.2016.06.018, 2016.
Ng, N. L., Kroll, J. H., Chan, A. W. H., Chhabra, P. S., Flagan, R. C., and Seinfeld, J. H.: Secondary organic aerosol formation from m-xylene, toluene, and benzene, Atmos. Chem. Phys., 7, 3909–3922, https://doi.org/10.5194/acp-7-3909-2007, 2007.
Nguyen, Q. T., Kjaer, K. H., Kling, K. I., Boesen, T., and Bilde, M.: Impact of fatty acid coating on the CCN activity of sea salt particles, Tellus B, 69, 1304064, https://doi.org/10.1080/16000889.2017.1304064, 2017.
Nguyen, T. B., Lee, P. B., Updyke, K. M., Bones, D. L., Laskin, J., Laskin, A., and Nizkorodov, S. A.: Formation of nitrogen- and sulfur-containing light-absorbing compounds accelerated by evaporation of water from secondary organic aerosols, J. Geophys. Res.-Atmos., 117, D01207, https://doi.org/10.1029/2011jd016944, 2012.
Osterroht, C.: Extraction of dissolved fatty acids from sea water, Fresenius J. Anal. Chem., 345, 773–779, https://doi.org/10.1007/bf00323009, 1993.
Pereira, L. S. A., Camacho, S. A., Malfatti-Gasperini, A. A., Jochelavicius, K., Nobre, T. M., Oliveira, O. N., and Aoki, P. H. B.: Evidence of photoinduced lipid hydroperoxidation in Langmuir monolayers containing Eosin Y, Colloid Surface B, 171, 682–689, https://doi.org/10.1016/j.colsurfb.2018.08.002, 2018.
Pillar, E. A., and Guzman, M. I.: Oxidation of Substituted Catechols at the Air-Water Interface: Production of Carboxylic Acids, Quinones, and Polyphenols, Environ. Sci. Technol., 51, 4951–4959, https://doi.org/10.1021/acs.est.7b00232, 2017.
Pöschl, U.: Atmospheric aerosols: Composition, transformation, climate and health effects, Angew. Chem. Int., 44, 7520–7540, https://doi.org/10.1002/anie.200501122, 2005.
Rame, E.: The interpretation of dynamic contact angles measured by the Wilhelmy plate method, J. Colloid Interf. Sci., 185, 245–251, https://doi.org/10.1006/jcis.1996.4589, 1997.
Raymond, T. M. and Pandis, S. N.: Formation of cloud droplets by multicomponent organic particles, J. Geophys. Res.-Atmos., 108, 4469, https://doi.org/10.1029/2003jd003503, 2003.
Riske, K. A., Sudbrack, T. P., Archilha, N. L., Uchoa, A. F., Schroder, A. P., Marques, C. M., Baptista, M. S., and Itri, R.: Giant Vesicles under Oxidative Stress Induced by a Membrane-Anchored Photosensitizer, Biophys. J., 97, 1362–1370, https://doi.org/10.1016/j.bpj.2009.06.023, 2009.
Rossignol, S., Aregahegn, K. Z., Tinel, L., Fine, L., Noziere, B., and George, C.: Glyoxal Induced Atmospheric Photosensitized Chemistry Leading to Organic Aerosol Growth, Environ. Sci. Technol., 48, 3218–3227, https://doi.org/10.1021/es405581g, 2014.
Rossignol, S., Tinel, L., Bianco, A., Passananti, M., Brigante, M., Donaldson, D. J., and George, C.: Atmospheric photochemistry at a fatty acid-coated air-water interface, Science, 353, 699–702, https://doi.org/10.1126/science.aaf3617, 2016.
Ruehl, C. R. and Wilson, K. R.: Surface Organic Mono layers Control the Hygroscopic Growth of Submicrometer Particles at High Relative Humidity, J. Phys. Chem. A, 118, 3952–3966, https://doi.org/10.1021/jp502844g, 2014.
Sannigrahi, P., Sullivan, A. P., Weber, R. J., and Ingall, E. D.: Characterization of water-soluble organic carbon in urban atmospheric aerosols using solid-state C-13 NMR spectroscopy, Environ. Sci. Technol., 40, 666–672, https://doi.org/10.1021/es051150i, 2006.
Sarrafzadeh, M., Wildt, J., Pullinen, I., Springer, M., Kleist, E., Tillmann, R., Schmitt, S. H., Wu, C., Mentel, T. F., Zhao, D., Hastie, D. R., and Kiendler-Scharr, A.: Impact of NOx and OH on secondary organic aerosol formation from β-pinene photooxidation, Atmos. Chem. Phys., 16, 11237–11248, https://doi.org/10.5194/acp-16-11237-2016, 2016.
Sebastiani, F., Campbell, R. A., Rastogi, K., and Pfrang, C.: Nighttime oxidation of surfactants at the air–water interface: effects of chain length, head group and saturation, Atmos. Chem. Phys., 18, 3249–3268, https://doi.org/10.5194/acp-18-3249-2018, 2018.
Shrestha, M., Luo, M., Li, Y., Xiang, B., Xiong, W., and Grassian, V. H.: Let there be light: stability of palmitic acid monolayers at the air/salt water interface in the presence and absence of simulated solar light and a photosensitizer, Chem. Sci., 9, 5716–5723, https://doi.org/10.1039/c8sc01957f, 2018.
Simon-Kutscher, J., Gericke, A., and Huhnerfuss, H.: Effect of bivalent Ba, Cu, Ni, and Zn cations on the structure of octadecanoic acid monolayers at the air-water interface as determined by external infrared reflection-absorption spectroscopy, Langmuir, 12, 1027–1034, https://doi.org/10.1021/la950731q, 1996.
Slowey, J. F., Jeffrey, L. M., and Hood, D. W.: The fatty-acid content of ocean water, Geochim. Cosmochim. Ac., 26, 607–616, https://doi.org/10.1016/0016-7037(62)90041-8, 1962.
Smith, J. D., Sio, V., Yu, L., Zhang, Q., and Anastasio, C.: Secondary Organic Aerosol Production from Aqueous Reactions of Atmospheric Phenols with an Organic Triplet Excited State, Environ. Sci. Technol., 48, 1049–1057, https://doi.org/10.1021/es4045715, 2014.
Snyder, R. G., Hsu, S. L., and Krimm, S.: Vibrational spectra in the C-H stretching region and the structure of the polymethylene chain, Spectrochim. Acta A, 34, 395–406, https://doi.org/10.1016/0584-8539(78)80167-6, 1978.
Sobanska, S., Barbillat, J., Moreau, M., Nuns, N., De Waele, I., Petitprez, D., Tobon, Y., and Bremard, C.: Influence of stearic acid coating of the NaCl surface on the reactivity with NO2 under humidity, Phys. Chem. Chem. Phys., 17, 10963–10977, https://doi.org/10.1039/c4cp05655h, 2015.
Song, M. J., Marcolli, C., Krieger, U. K., Lienhard, D. M., and Peter, T.: Morphologies of mixed organic/inorganic/aqueous aerosol droplets, Faraday Discuss., 165, 289–316, https://doi.org/10.1039/c3fd00049d, 2013.
Tervahattu, H., Juhanoja, J., Vaida, V., Tuck, A. F., Niemi, J. V., Kupiainen, K., Kulmala, M., and Vehkamaki, H.: Fatty acids on continental sulfate aerosol particles, J. Geophys. Res.-Atmos., 110, D06207, https://doi.org/10.1029/2004jd005400, 2005.
Tinel, L., Dumas, S., and George, C.: A time-resolved study of the multiphase chemistry of excited carbonyls: Imidazole-2-carboxaldehyde and halides, CR Chim., 17, 801–807, https://doi.org/10.1016/j.crci.2014.03.008, 2014.
Tinel, L., Rossignol, S., Bianco, A., Passananti, M., Perrier, S., Wang, X., Brigante, M., Donaldson, D. J., and George, C.: Mechanistic Insights on the Photosensitized Chemistry of a Fatty Acid at the Air/Water Interface, Environ. Sci. Technol., 50, 11041–11048, https://doi.org/10.1021/acs.est.6b03165, 2016.
Toossi, R. and Novakov, T.: The lifetime of aerosols in ambient air: consideration of the effects of surfactants and chemical reactions, Atmos. Environ., 19, 127–133, https://doi.org/10.1016/0004-6981(85)90143-x, 1985.
Tsui, W. G. and McNeill, V. F.: Modeling Secondary Organic Aerosol Production from Photosensitized Humic-like Substances (HULIS), Environ. Sci. Tech. Let., 5, 255–259, https://doi.org/10.1021/acs.estlett.8b00101, 2018.
Tsui, W. G., Rao, Y., Dai, H. L., and McNeill, V. F.: Modeling Photosensitized Secondary Organic Aerosol Formation in Laboratory and Ambient Aerosols, Environ. Sci. Technol., 51, 7496–7501, https://doi.org/10.1021/acs.est.7b01416, 2017.
Vione, D., Maurino, V., and Minero, C.: Photosensitised humic-like substances (HULIS) formation processes of atmospheric significance: a review, Environ. Sci. Pollut. R., 21, 11614–11622, https://doi.org/10.1007/s11356-013-2319-0, 2014.
Wang, N. J. and Yu, J. Z.: Size distributions of hydrophilic and hydrophobic fractions of water-soluble organic carbon in an urban atmosphere in Hong Kong, Atmos. Environ., 166, 110–119, https://doi.org/10.1016/j.atmosenv.2017.07.009, 2017.
Wang, S. Y., Du, L., Zhu, J. Q., Tsona, N. T., Liu, S. J., Wang, Y. F., Ge, M. F., and Wang, W. X.: Gas-Phase Oxidation of Allyl Acetate by O3, OH, Cl, and NO3: Reaction Kinetics and Mechanism, J. Phys. Chem. A, 122, 1600–1611, https://doi.org/10.1021/acs.jpca.7b10599, 2018.
Wong-Ekkabut, J., Xu, Z., Triampo, W., Tang, I. M., Tieleman, D. P., and Monticelli, L.: Effect of lipid peroxidation on the properties of lipid bilayers: A molecular dynamics study, Biophys. J., 93, 4225–4236, https://doi.org/10.1529/biophysj.107.112565, 2007.
Wu, S. P., Schwab, J., Liu, B. L., Li, T. C., and Yuan, C. S.: Seasonal variations and source identification of selected organic acids associated with PM10 in the coastal area of Southeastern China, Atmos. Res., 155, 37–51, https://doi.org/10.1016/j.atmosres.2014.11.014, 2015.
Yin, T., Cao, X., Liu, X., Wang, J., Shi, C., Su, J., Zhang, Y., Gou, J., He, H., Guo, H., Tang, X., and Zhao, Y.: Interfacial molecular interactions based on the conformation recognition between the insoluble antitumor drug AD-1 and DSPC, Colloid Surface B, 146, 902–909, https://doi.org/10.1016/j.colsurfb.2016.07.040, 2016.
Yu, J. Z., Yang, H., Zhang, H. Y., and Lau, A. K. H.: Size distributions of water-soluble organic carbon in ambient aerosols and its size-resolved thermal characteristics, Atmos. Environ., 38, 1061–1071, https://doi.org/10.1016/j.atmosenv.2003.10.049, 2004.
Yu, L., Smith, J., Laskin, A., Anastasio, C., Laskin, J., and Zhang, Q.: Chemical characterization of SOA formed from aqueous-phase reactions of phenols with the triplet excited state of carbonyl and hydroxyl radical, Atmos. Chem. Phys., 14, 13801–13816, https://doi.org/10.5194/acp-14-13801-2014, 2014.
Zhu, J. Q., Wang, S. Y., Tsona, N. T., Jiang, X. T., Wang, Y. F., Ge, M. F., and Du, L.: Gas-Phase Reaction of Methyl n-Propyl Ether with OH, NO3, and Cl: Kinetics and Mechanism, J. Phys. Chem. A, 121, 6800–6809, https://doi.org/10.1021/acs.jpca.7b06877, 2017.
Zhu, W. Z., Yang, G. P., and Zhang, H. H.: Photochemical behavior of dissolved and colloidal organic matter in estuarine and oceanic waters, Sci. Total Environ., 607, 214–224, https://doi.org/10.1016/j.scitotenv.2017.06.163, 2017.