Articles | Volume 11, issue 21
https://doi.org/10.5194/acp-11-11069-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/acp-11-11069-2011
© Author(s) 2011. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Secondary organic aerosol formation in cloud droplets and aqueous particles (aqSOA): a review of laboratory, field and model studies
B. Ervens
CIRES, University of Colorado, Boulder, CO, USA
NOAA, ESRL/CSD Boulder, CO, USA
B. J. Turpin
Department of Environmental Sciences, Rutgers University, New Brunswick, NJ, USA
R. J. Weber
Georgia Institute of Technology, School of Earth and Atmospheric Sciences, Atlanta, GA, USA
Related subject area
Subject: Aerosols | Research Activity: Laboratory Studies | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
Characterization of the particle size distribution, mineralogy, and Fe mode of occurrence of dust-emitting sediments from the Mojave Desert, California, USA
Measurement report: Effects of transition metal ions on the optical properties of humic-like substances (HULIS) reveal a structural preference – a case study of PM2.5 in Beijing, China
The Impact of Aqueous Phase Replacement Reaction on the Phase State of Internally Mixed Organic/ammonium Aerosols
Probing Iceland's dust-emitting sediments: particle size distribution, mineralogy, cohesion, Fe mode of occurrence, and reflectance spectra signatures
Photoenhanced sulfate formation by the heterogeneous uptake of SO2 on non-photoactive mineral dust
Comparison of water-soluble and water-insoluble organic compositions attributing to different light absorption efficiency between residential coal and biomass burning emissions
Technical note: High-resolution analyses of concentrations and sizes of black carbon particles deposited on northwest Greenland over the past 350 years – Part 1. Continuous flow analysis of the SIGMA-D ice core using a Wide-Range Single-Particle Soot Photometer and a high-efficiency nebulizer
Suppressed atmospheric chemical aging of cooking organic aerosol particles in wintertime conditions
Formation and loss of light absorbance by phenolic aqueous SOA by ●OH and an organic triplet excited state
Nocturnal Atmospheric Synergistic Oxidation Reduces the Formation of Low-volatility Organic Compounds from Biogenic Emissions
Technical Note: A technique to convert NO2 to NO2− with S(IV) and its application to measuring nitrate photolysis
Measurement report: The Fifth International Workshop on Ice Nucleation Phase 1 (FIN-01): Intercomparison of Single Particle Mass Spectrometers
Distribution, chemical, and molecular composition of high and low molecular weight humic-like substances in ambient aerosols
Desorption lifetimes and activation energies influencing gas–surface interactions and multiphase chemical kinetics
Molecular analysis of secondary organic aerosol and brown carbon from the oxidation of indole
Secondary organic aerosol formed by Euro 5 gasoline vehicle emissions: chemical composition and gas-to-particle phase partitioning
Assessment of the contribution of residential waste burning to ambient PM10 concentrations in Hungary and Romania
Source differences in the components and cytotoxicity of PM2.5 from automobile exhaust, coal combustion, and biomass burning contributing to urban aerosol toxicity
Chamber studies of OH + dimethyl sulfoxide and dimethyl disulfide: insights into the dimethyl sulfide oxidation mechanism
Low-temperature ice nucleation of sea spray and secondary marine aerosols under cirrus cloud conditions
Temperature-dependent aqueous OH kinetics of C2–C10 linear and terpenoid alcohols and diols: new rate coefficients, structure–activity relationship, and atmospheric lifetimes
A possible unaccounted source of nitrogen-containing compound formation in aerosols: amines reacting with secondary ozonides
Seasonal variations in photooxidant formation and light absorption in aqueous extracts of ambient particles
Variability in sediment particle size, mineralogy, and Fe mode of occurrence across dust-source inland drainage basins: the case of the lower Drâa Valley, Morocco
Gas–particle partitioning of toluene oxidation products: an experimental and modeling study
Chemically speciated air pollutant emissions from open burning of household solid waste from South Africa
Bulk and molecular-level composition of primary organic aerosol from wood, straw, cow dung, and plastic burning
Volatile oxidation products and secondary organosiloxane aerosol from D5 + OH at varying OH exposures
Molecular fingerprints and health risks of smoke from home-use incense burning
High enrichment of heavy metals in fine particulate matter through dust aerosol generation
Production of ice-nucleating particles (INPs) by fast-growing phytoplankton
Technical note: In situ measurements and modelling of the oxidation kinetics in films of a cooking aerosol proxy using a quartz crystal microbalance with dissipation monitoring (QCM-D)
Particulate emissions from cooking activities: emission factors, emission dynamics, and mass spectrometric analysis for different preparation methods
Contrasting impacts of humidity on the ozonolysis of monoterpenes: insights into the multi-generation chemical mechanism
Quantifying the seasonal variations in and regional transport of PM2.5 in the Yangtze River Delta region, China: characteristics, sources, and health risks
Opinion: Atmospheric multiphase chemistry – past, present, and future
Distinct photochemistry in glycine particles mixed with different atmospheric nitrate salts
Effects of storage conditions on the molecular-level composition of organic aerosol particles
Characterization of gas and particle emissions from open burning of household solid waste from South Africa
Chemically distinct particle-phase emissions from highly controlled pyrolysis of three wood types
Predicting photooxidant concentrations in aerosol liquid water based on laboratory extracts of ambient particles
Physicochemical characterization of free troposphere and marine boundary layer ice-nucleating particles collected by aircraft in the eastern North Atlantic
Large differences of highly oxygenated organic molecules (HOMs) and low-volatile species in secondary organic aerosols (SOAs) formed from ozonolysis of β-pinene and limonene
Impact of fossil and non-fossil fuel sources on the molecular compositions of water-soluble humic-like substances in PM2.5 at a suburban site of Yangtze River Delta, China
Technical note: Improved synthetic routes to cis- and trans-(2-methyloxirane-2,3-diyl)dimethanol (cis- and trans-β-isoprene epoxydiol)
Technical note: Intercomparison study of the elemental carbon radiocarbon analysis methods using synthetic known samples
Chemical evolution of primary and secondary biomass burning aerosols during daytime and nighttime
Formation of highly oxygenated organic molecules from the oxidation of limonene by OH radical: significant contribution of H-abstraction pathway
Measurement report: Atmospheric aging of combustion-derived particles – impact on stable free radical concentration and its ability to produce reactive oxygen species in aqueous media
Photoaging of phenolic secondary organic aerosol in the aqueous phase: evolution of chemical and optical properties and effects of oxidants
Adolfo González-Romero, Cristina González-Flórez, Agnesh Panta, Jesús Yus-Díez, Patricia Córdoba, Andres Alastuey, Natalia Moreno, Melani Hernández-Chiriboga, Konrad Kandler, Martina Klose, Roger N. Clark, Bethany L. Ehlmann, Rebecca N. Greenberger, Abigail M. Keebler, Phil Brodrick, Robert Green, Paul Ginoux, Xavier Querol, and Carlos Pérez García-Pando
Atmos. Chem. Phys., 24, 9155–9176, https://doi.org/10.5194/acp-24-9155-2024, https://doi.org/10.5194/acp-24-9155-2024, 2024
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In this research, we studied the dust-emitting properties of crusts and aeolian ripples from the Mojave Desert. These properties are key to understanding the effect of dust upon climate. We found two different playa lakes according to the groundwater regime, which implies differences in crusts' cohesion state and mineralogy, which can affect the dust emission potential and properties. We also compare them with Moroccan Sahara crusts and Icelandic top sediments.
This article is included in the Encyclopedia of Geosciences
Juanjuan Qin, Leiming Zhang, Yuanyuan Qin, Shaoxuan Shi, Jingnan Li, Zhao Shu, Yuwei Gao, Ting Qi, Jihua Tan, and Xinming Wang
Atmos. Chem. Phys., 24, 7575–7589, https://doi.org/10.5194/acp-24-7575-2024, https://doi.org/10.5194/acp-24-7575-2024, 2024
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The present research unveiled that acidity dominates while transition metal ions harmonize with the light absorption properties of humic-like substances (HULIS). Cu2+ has quenching effects on HULIS by complexation, hydrogen substitution, or electrostatic adsorption, with aromatic structures of HULIS. Such effects are less pronounced if from Mn2+, Ni2+, Zn2+, and Cu2+. Oxidized HULIS might contain electron-donating groups, whereas N-containing compounds might contain electron-withdrawing groups.
This article is included in the Encyclopedia of Geosciences
Hui Yang, Fengfeng Dong, Li Xia, Qishen Huang, Shufeng Pang, and Yunhong Zhang
EGUsphere, https://doi.org/10.5194/egusphere-2024-1556, https://doi.org/10.5194/egusphere-2024-1556, 2024
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Atmospheric secondary aerosols often contain a mix of organic and inorganic components, which can undergo complex reactions, leading to significant uncertainty in their phase state. Using molecular spectroscopic methods, we demonstrated that the aqueous replacement reaction, unique to these mixed aerosols and promoted by the presence of ammonium, significantly alters their phase behavior. This effect complicates the prediction of aerosol phase states and the corresponding atmospheric processes.
This article is included in the Encyclopedia of Geosciences
Adolfo González-Romero, Cristina González-Flórez, Agnesh Panta, Jesús Yus-Díez, Patricia Córdoba, Andres Alastuey, Natalia Moreno, Konrad Kandler, Martina Klose, Roger N. Clark, Bethany L. Ehlmann, Rebecca N. Greenberger, Abigail M. Keebler, Phil Brodrick, Robert O. Green, Xavier Querol, and Carlos Pérez García-Pando
Atmos. Chem. Phys., 24, 6883–6910, https://doi.org/10.5194/acp-24-6883-2024, https://doi.org/10.5194/acp-24-6883-2024, 2024
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The knowledge of properties from dust emitted in high latitudes such as in Iceland is scarce. This study focuses on the particle size, mineralogy, cohesion, and iron mode of occurrence and reflectance spectra of dust-emitting sediments. Icelandic top sediments have lower cohesion state, coarser particle size, distinctive mineralogy, and 3-fold bulk Fe content, with a large presence of magnetite compared to Saharan crusts.
This article is included in the Encyclopedia of Geosciences
Wangjin Yang, Jiawei Ma, Hongxing Yang, Fu Li, and Chong Han
Atmos. Chem. Phys., 24, 6757–6768, https://doi.org/10.5194/acp-24-6757-2024, https://doi.org/10.5194/acp-24-6757-2024, 2024
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We provide evidence that light enhances the conversion of SO2 to sulfates on non-photoactive mineral dust, where triplet states of SO2 (3SO2) can act as a pivotal trigger to generate sulfates. Photochemical sulfate formation depends on H2O, O2, and basicity of mineral dust. The SO2 photochemistry on non-photoactive mineral dust contributes to sulfates, highlighting previously unknown pathways to better explain the missing sources of atmospheric sulfates.
This article is included in the Encyclopedia of Geosciences
Lu Zhang, Jin Li, Yaojie Li, Xinlei Liu, Zhihan Luo, Guofeng Shen, and Shu Tao
Atmos. Chem. Phys., 24, 6323–6337, https://doi.org/10.5194/acp-24-6323-2024, https://doi.org/10.5194/acp-24-6323-2024, 2024
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Brown carbon (BrC) is related to radiative forcing and climate change. The BrC fraction from residential coal and biomass burning emissions, which were the major source of BrC, was characterized at the molecular level. The CHOS aromatic compounds explained higher light absorption efficiencies of biomass burning emissions compared to coal. The unique formulas of coal combustion aerosols were characterized by higher unsaturated compounds, and such information could be used for source appointment.
This article is included in the Encyclopedia of Geosciences
Kumiko Goto-Azuma, Remi Dallmayr, Yoshimi Ogawa-Tsukagawa, Nobuhiro Moteki, Tatsuhiro Mori, Sho Ohata, Yutaka Kondo, Makoto Koike, Motohiro Hirabayashi, Jun Ogata, Kyotaro Kitamura, Kenji Kawamura, Koji Fujita, Sumito Matoba, Naoko Nagatsuka, Akane Tsushima, Kaori Fukuda, and Teruo Aoki
EGUsphere, https://doi.org/10.5194/egusphere-2024-1496, https://doi.org/10.5194/egusphere-2024-1496, 2024
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We developed a continuous flow analysis system to analyse an ice core from northwest Greenland, and coupled it with an improved BC measurement technique. This coupling allowed accurate high-resolution analyses of BC particles' size distributions and concentrations with diameters between 70 nm and 4 μm for the past 350 years. Our results provide crucial insights into BC's climatic effects. We also found that previous ice core studies substantially underestimated the BC mass concentrations.
This article is included in the Encyclopedia of Geosciences
Wenli Liu, Longkun He, Yingjun Liu, Keren Liao, Qi Chen, and Mikinori Kuwata
Atmos. Chem. Phys., 24, 5625–5636, https://doi.org/10.5194/acp-24-5625-2024, https://doi.org/10.5194/acp-24-5625-2024, 2024
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Cooking is a major source of particles in urban areas. Previous studies demonstrated that the chemical lifetimes of cooking organic aerosols (COAs) were much shorter (~minutes) than the values reported by field observations (~hours). We conducted laboratory experiments to resolve the discrepancy by considering suppressed reactivity under low temperature. The parameterized k2–T relationships and observed surface temperature data were used to estimate the chemical lifetimes of COA particles.
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Stephanie Arciva, Lan Ma, Camille Mavis, Chrystal Guzman, and Cort Anastasio
Atmos. Chem. Phys., 24, 4473–4485, https://doi.org/10.5194/acp-24-4473-2024, https://doi.org/10.5194/acp-24-4473-2024, 2024
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We measured changes in light absorption during the aqueous oxidation of six phenols with hydroxyl radical (●OH) or an organic triplet excited state (3C*). All the phenols formed light-absorbing secondary brown carbon (BrC), which then decayed with continued oxidation. Extrapolation to ambient conditions suggest ●OH is the dominant sink of secondary phenolic BrC in fog/cloud drops, while 3C* controls the lifetime of this light absorption in particle water.
This article is included in the Encyclopedia of Geosciences
Han Zang, Zekun Luo, Chenxi Li, Ziyue Li, Dandan Huang, and Yue Zhao
EGUsphere, https://doi.org/10.5194/egusphere-2024-1131, https://doi.org/10.5194/egusphere-2024-1131, 2024
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Atmospheric organics are subject to synergistic oxidation by different oxidants, yet the mechanisms of such processes are poorly understood. Here, using direct measurements and kinetic modelling, we probe the nocturnal synergistic oxidation mechanism of α-pinene by O3 and NO3 radicals and in particular the fate of peroxy radical intermediates of different origins, which will deepen our understanding of the monoterpene oxidation chemistry and its contribution to atmospheric particle formation.
This article is included in the Encyclopedia of Geosciences
Aaron Lieberman, Julietta Picco, Murat Onder, and Cort Anastasio
Atmos. Chem. Phys., 24, 4411–4419, https://doi.org/10.5194/acp-24-4411-2024, https://doi.org/10.5194/acp-24-4411-2024, 2024
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We developed a method that uses aqueous S(IV) to quantitatively convert NO2 to NO2−, which allows both species to be quantified using the Griess method. As an example of the utility of the method, we quantified both photolysis channels of nitrate, with and without a scavenger for hydroxyl radical (·OH). The results show that without a scavenger, ·OH reacts with nitrite to form nitrogen dioxide, suppressing the apparent quantum yield of NO2− and enhancing that of NO2.
This article is included in the Encyclopedia of Geosciences
Xiaoli Shen, David M. Bell, Hugh Coe, Naruki Hiranuma, Fabian Mahrt, Nicholas A. Marsden, Claudia Mohr, Daniel M. Murphy, Harald Saathoff, Johannes Schneider, Jacqueline Wilson, Maria A. Zawadowicz, Alla Zelenyuk, Paul J. DeMott, Ottmar Möhler, and Daniel J. Cziczo
EGUsphere, https://doi.org/10.5194/egusphere-2024-928, https://doi.org/10.5194/egusphere-2024-928, 2024
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Single particle mass spectrometer (SPMS) is commonly used to measure chemical composition and mixing state of aerosol particles. Intercomparison of SPMSs was conducted. All instruments reported similar size ranges and common spectral features. The instrument-specific detection efficiency was found to be more dependent on particle size than type. All instruments differentiated secondary organic aerosol, soot, and soil dust, but had difficulties differentiating among specific minerals and dusts.
This article is included in the Encyclopedia of Geosciences
Xingjun Fan, Ao Cheng, Xufang Yu, Tao Cao, Dan Chen, Wenchao Ji, Yongbing Cai, Fande Meng, Jianzhong Song, and Ping'an Peng
Atmos. Chem. Phys., 24, 3769–3783, https://doi.org/10.5194/acp-24-3769-2024, https://doi.org/10.5194/acp-24-3769-2024, 2024
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Molecular-level characteristics of high molecular weight (HMW) and low MW (LMW) humic-like substances (HULIS) were comprehensively investigated, where HMW HULIS had larger chromophores and larger molecular size than LMW HULIS and exhibited higher aromaticity and humification. Electrospray ionization high-resolution mass spectrometry revealed more aromatic molecules in HMW HULIS. HMW HULIS had more CHON compounds, while LMW HULIS had more CHO compounds.
This article is included in the Encyclopedia of Geosciences
Daniel A. Knopf, Markus Ammann, Thomas Berkemeier, Ulrich Pöschl, and Manabu Shiraiwa
Atmos. Chem. Phys., 24, 3445–3528, https://doi.org/10.5194/acp-24-3445-2024, https://doi.org/10.5194/acp-24-3445-2024, 2024
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The initial step of interfacial and multiphase chemical processes involves adsorption and desorption of gas species. This study demonstrates the role of desorption energy governing the residence time of the gas species at the environmental interface. A parameterization is formulated that enables the prediction of desorption energy based on the molecular weight, polarizability, and oxygen-to-carbon ratio of the desorbing chemical species. Its application to gas–particle interactions is discussed.
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Feng Jiang, Kyla Siemens, Claudia Linke, Yanxia Li, Yiwei Gong, Thomas Leisner, Alexander Laskin, and Harald Saathoff
Atmos. Chem. Phys., 24, 2639–2649, https://doi.org/10.5194/acp-24-2639-2024, https://doi.org/10.5194/acp-24-2639-2024, 2024
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We investigated the optical properties, chemical composition, and formation mechanisms of secondary organic aerosol (SOA) and brown carbon (BrC) from the oxidation of indole with and without NO2 in the Aerosol Interaction and Dynamics in the Atmosphere (AIDA) simulation chamber. This work is one of the very few to link the optical properties and chemical composition of indole SOA with and without NO2 by simulation chamber experiments.
This article is included in the Encyclopedia of Geosciences
Evangelia Kostenidou, Baptiste Marques, Brice Temime-Roussel, Yao Liu, Boris Vansevenant, Karine Sartelet, and Barbara D'Anna
Atmos. Chem. Phys., 24, 2705–2729, https://doi.org/10.5194/acp-24-2705-2024, https://doi.org/10.5194/acp-24-2705-2024, 2024
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Secondary organic aerosol (SOA) from gasoline vehicles can be a significant source of particulate matter in urban areas. Here the chemical composition of secondary volatile organic compounds and SOA produced by photo-oxidation of Euro 5 gasoline vehicle emissions was studied. The volatility of the SOA formed was calculated. Except for the temperature and the concentration of the aerosol, additional parameters may play a role in the gas-to-particle partitioning.
This article is included in the Encyclopedia of Geosciences
András Hoffer, Aida Meiramova, Ádám Tóth, Beatrix Jancsek-Turóczi, Gyula Kiss, Ágnes Rostási, Erika Andrea Levei, Luminita Marmureanu, Attila Machon, and András Gelencsér
Atmos. Chem. Phys., 24, 1659–1671, https://doi.org/10.5194/acp-24-1659-2024, https://doi.org/10.5194/acp-24-1659-2024, 2024
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Specific tracer compounds identified previously in controlled test burnings of different waste types in the laboratory were detected and quantified in ambient PM10 samples collected in five Hungarian and four Romanian settlements. Back-of-the-envelope calculations based on the relative emission factors of individual tracers suggested that the contribution of solid waste burning particulate emissions to ambient PM10 mass concentrations may be as high as a few percent.
This article is included in the Encyclopedia of Geosciences
Xiao-San Luo, Weijie Huang, Guofeng Shen, Yuting Pang, Mingwei Tang, Weijun Li, Zhen Zhao, Hanhan Li, Yaqian Wei, Longjiao Xie, and Tariq Mehmood
Atmos. Chem. Phys., 24, 1345–1360, https://doi.org/10.5194/acp-24-1345-2024, https://doi.org/10.5194/acp-24-1345-2024, 2024
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PM2.5 are air pollutants threatening health globally, but they are a mixture of chemical compositions from many sources and result in unequal toxicity. Which composition from which source of PM2.5 as the most hazardous object is a question hindering effective pollution control policy-making. With chemical and toxicity experiments, we found automobile exhaust and coal combustion to be priority emissions with higher toxic compositions for precise air pollution control, ensuring public health.
This article is included in the Encyclopedia of Geosciences
Matthew B. Goss and Jesse H. Kroll
Atmos. Chem. Phys., 24, 1299–1314, https://doi.org/10.5194/acp-24-1299-2024, https://doi.org/10.5194/acp-24-1299-2024, 2024
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The chemistry driving dimethyl sulfide (DMS) oxidation and subsequent sulfate particle formation in the atmosphere is poorly constrained. We oxidized two related compounds (dimethyl sulfoxide and dimethyl disulfide) in the laboratory under varied NOx conditions and measured the gas- and particle-phase products. These results demonstrate that both the OH addition and OH abstraction pathways for DMS oxidation contribute to particle formation via mechanisms that do not involve the SO2 intermediate.
This article is included in the Encyclopedia of Geosciences
Ryan J. Patnaude, Kathryn A. Moore, Russell J. Perkins, Thomas C. J. Hill, Paul J. DeMott, and Sonia M. Kreidenweis
Atmos. Chem. Phys., 24, 911–928, https://doi.org/10.5194/acp-24-911-2024, https://doi.org/10.5194/acp-24-911-2024, 2024
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In this study we examined the effect of atmospheric aging on sea spray aerosols (SSAs) to form ice and how newly formed secondary marine aerosols (SMAs) may freeze at cirrus temperatures (< −38 °C). Results show that SSAs freeze at different relative humidities (RHs) depending on the temperature and that the ice-nucleating ability of SSA was not hindered by atmospheric aging. SMAs are shown to freeze at high RHs and are likely inefficient at forming ice at cirrus temperatures.
This article is included in the Encyclopedia of Geosciences
Bartłomiej Witkowski, Priyanka Jain, Beata Wileńska, and Tomasz Gierczak
Atmos. Chem. Phys., 24, 663–688, https://doi.org/10.5194/acp-24-663-2024, https://doi.org/10.5194/acp-24-663-2024, 2024
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This article reports the results of the kinetic measurements for the aqueous oxidation of the 29 aliphatic alcohols by hydroxyl radical (OH) at different temperatures. The data acquired and the literature data were used to optimize a model for predicting the aqueous OH reactivity of alcohols and carboxylic acids and to estimate the atmospheric lifetimes of five terpenoic alcohols. The kinetic data provided new insights into the mechanism of aqueous oxidation of aliphatic molecules by the OH.
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Junting Qiu, Xinlin Shen, Jiangyao Chen, Guiying Li, and Taicheng An
Atmos. Chem. Phys., 24, 155–166, https://doi.org/10.5194/acp-24-155-2024, https://doi.org/10.5194/acp-24-155-2024, 2024
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We studied reactions of secondary ozonides (SOZs) with amines. SOZs formed from ozonolysis of β-caryophyllene and α-humulene are found to be reactive to ethylamine and methylamine. Products from SOZs with various conformations reacting with the same amine had different functional groups. Our findings indicate that interaction of SOZs with amines in the atmosphere is very complicated, which is potentially a hitherto unrecognized source of N-containing compound formation.
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Lan Ma, Reed Worland, Laura Heinlein, Chrystal Guzman, Wenqing Jiang, Christopher Niedek, Keith J. Bein, Qi Zhang, and Cort Anastasio
Atmos. Chem. Phys., 24, 1–21, https://doi.org/10.5194/acp-24-1-2024, https://doi.org/10.5194/acp-24-1-2024, 2024
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We measured concentrations of three photooxidants – the hydroxyl radical, triplet excited states of organic carbon, and singlet molecular oxygen – in fine particles collected over a year. Concentrations are highest in extracts of fresh biomass burning particles, largely because they have the highest particle concentrations and highest light absorption. When normalized by light absorption, rates of formation for each oxidant are generally similar for the four particle types we observed.
This article is included in the Encyclopedia of Geosciences
Adolfo González-Romero, Cristina González-Flórez, Agnesh Panta, Jesús Yus-Díez, Cristina Reche, Patricia Córdoba, Natalia Moreno, Andres Alastuey, Konrad Kandler, Martina Klose, Clarissa Baldo, Roger N. Clark, Zongbo Shi, Xavier Querol, and Carlos Pérez García-Pando
Atmos. Chem. Phys., 23, 15815–15834, https://doi.org/10.5194/acp-23-15815-2023, https://doi.org/10.5194/acp-23-15815-2023, 2023
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The effect of dust emitted from desertic surfaces upon climate and ecosystems depends on size and mineralogy, but data from soil mineral atlases of desert soils are scarce. We performed particle-size distribution, mineralogy, and Fe speciation in southern Morocco. Results show coarser particles with high quartz proportion are near the elevated areas, while in depressed areas, sizes are finer, and proportions of clays and nano-Fe oxides are higher. This difference is important for dust modelling.
This article is included in the Encyclopedia of Geosciences
Victor Lannuque, Barbara D'Anna, Evangelia Kostenidou, Florian Couvidat, Alvaro Martinez-Valiente, Philipp Eichler, Armin Wisthaler, Markus Müller, Brice Temime-Roussel, Richard Valorso, and Karine Sartelet
Atmos. Chem. Phys., 23, 15537–15560, https://doi.org/10.5194/acp-23-15537-2023, https://doi.org/10.5194/acp-23-15537-2023, 2023
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Large uncertainties remain in understanding secondary organic aerosol (SOA) formation from toluene oxidation. In this study, speciation measurements in gaseous and particulate phases were carried out, providing partitioning and volatility data on individual toluene SOA components at different temperatures. A new detailed oxidation mechanism was developed to improve modeled speciation, and effects of different processes involved in gas–particle partitioning at the molecular scale are explored.
This article is included in the Encyclopedia of Geosciences
Xiaoliang Wang, Hatef Firouzkouhi, Judith C. Chow, John G. Watson, Steven Sai Hang Ho, Warren Carter, and Alexandra S. M. De Vos
Atmos. Chem. Phys., 23, 15375–15393, https://doi.org/10.5194/acp-23-15375-2023, https://doi.org/10.5194/acp-23-15375-2023, 2023
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Open burning of municipal solid waste emits chemicals that are harmful to the environment. This paper reports source profiles and emission factors for PM2.5 species and acidic/alkali gases from laboratory combustion of 10 waste categories (including plastics and biomass) that represent open burning in South Africa. Results will be useful for health and climate impact assessments, speciated emission inventories, source-oriented dispersion models, and receptor-based source apportionment.
This article is included in the Encyclopedia of Geosciences
Jun Zhang, Kun Li, Tiantian Wang, Erlend Gammelsæter, Rico K. Y. Cheung, Mihnea Surdu, Sophie Bogler, Deepika Bhattu, Dongyu S. Wang, Tianqu Cui, Lu Qi, Houssni Lamkaddam, Imad El Haddad, Jay G. Slowik, Andre S. H. Prevot, and David M. Bell
Atmos. Chem. Phys., 23, 14561–14576, https://doi.org/10.5194/acp-23-14561-2023, https://doi.org/10.5194/acp-23-14561-2023, 2023
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We conducted burning experiments to simulate various types of solid fuel combustion, including residential burning, wildfires, agricultural burning, cow dung, and plastic bag burning. The chemical composition of the particles was characterized using mass spectrometers, and new potential markers for different fuels were identified using statistical analysis. This work improves our understanding of emissions from solid fuel burning and offers support for refined source apportionment.
This article is included in the Encyclopedia of Geosciences
Hyun Gu Kang, Yanfang Chen, Yoojin Park, Thomas Berkemeier, and Hwajin Kim
Atmos. Chem. Phys., 23, 14307–14323, https://doi.org/10.5194/acp-23-14307-2023, https://doi.org/10.5194/acp-23-14307-2023, 2023
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D5 is an emerging anthropogenic pollutant that is ubiquitous in indoor and urban environments, and the OH oxidation of D5 forms secondary organosiloxane aerosol (SOSiA). Application of a kinetic box model that uses a volatility basis set (VBS) showed that consideration of oxidative aging (aging-VBS) predicts SOSiA formation much better than using a standard-VBS model. Ageing-dependent parameterization is needed to accurately model SOSiA to assess the implications of siloxanes for air quality.
This article is included in the Encyclopedia of Geosciences
Kai Song, Rongzhi Tang, Jingshun Zhang, Zichao Wan, Yuan Zhang, Kun Hu, Yuanzheng Gong, Daqi Lv, Sihua Lu, Yu Tan, Ruifeng Zhang, Ang Li, Shuyuan Yan, Shichao Yan, Baoming Fan, Wenfei Zhu, Chak K. Chan, Maosheng Yao, and Song Guo
Atmos. Chem. Phys., 23, 13585–13595, https://doi.org/10.5194/acp-23-13585-2023, https://doi.org/10.5194/acp-23-13585-2023, 2023
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Incense burning is common in Asia, posing threats to human health and air quality. However, less is known about its emissions and health risks. Full-volatility organic species from incense-burning smoke are detected and quantified. Intermediate-volatility volatile organic compounds (IVOCs) are crucial organics accounting for 19.2 % of the total emission factors (EFs) and 40.0 % of the secondary organic aerosol (SOA) estimation, highlighting the importance of incorporating IVOCs into SOA models.
This article is included in the Encyclopedia of Geosciences
Qianqian Gao, Shengqiang Zhu, Kaili Zhou, Jinghao Zhai, Shaodong Chen, Qihuang Wang, Shurong Wang, Jin Han, Xiaohui Lu, Hong Chen, Liwu Zhang, Lin Wang, Zimeng Wang, Xin Yang, Qi Ying, Hongliang Zhang, Jianmin Chen, and Xiaofei Wang
Atmos. Chem. Phys., 23, 13049–13060, https://doi.org/10.5194/acp-23-13049-2023, https://doi.org/10.5194/acp-23-13049-2023, 2023
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Dust is a major source of atmospheric aerosols. Its chemical composition is often assumed to be similar to the parent soil. However, this assumption has not been rigorously verified. Dust aerosols are mainly generated by wind erosion, which may have some chemical selectivity. Mn, Cd and Pb were found to be highly enriched in fine-dust (PM2.5) aerosols. In addition, estimation of heavy metal emissions from dust generation by air quality models may have errors without using proper dust profiles.
This article is included in the Encyclopedia of Geosciences
Daniel C. O. Thornton, Sarah D. Brooks, Elise K. Wilbourn, Jessica Mirrielees, Alyssa N. Alsante, Gerardo Gold-Bouchot, Andrew Whitesell, and Kiana McFadden
Atmos. Chem. Phys., 23, 12707–12729, https://doi.org/10.5194/acp-23-12707-2023, https://doi.org/10.5194/acp-23-12707-2023, 2023
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A major uncertainty in our understanding of clouds and climate is the sources and properties of the aerosol on which clouds grow. We found that aerosol containing organic matter from fast-growing marine phytoplankton was a source of ice-nucleating particles (INPs). INPs facilitate freezing of ice crystals at warmer temperatures than otherwise possible and therefore change cloud formation and properties. Our results show that ecosystem processes and the properties of sea spray aerosol are linked.
This article is included in the Encyclopedia of Geosciences
Adam Milsom, Shaojun Qi, Ashmi Mishra, Thomas Berkemeier, Zhenyu Zhang, and Christian Pfrang
Atmos. Chem. Phys., 23, 10835–10843, https://doi.org/10.5194/acp-23-10835-2023, https://doi.org/10.5194/acp-23-10835-2023, 2023
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Aerosols and films are found indoors and outdoors. Our study measures and models reactions of a cooking aerosol proxy with the atmospheric oxidant ozone relying on a low-cost but sensitive technique based on mass changes and film rigidity. We found that film morphology changed and film rigidity increased with evidence of surface crust formation during ozone exposure. Our modelling results demonstrate clear potential to take this robust method to the field for reaction monitoring.
This article is included in the Encyclopedia of Geosciences
Julia Pikmann, Frank Drewnick, Friederike Fachinger, and Stephan Borrmann
EGUsphere, https://doi.org/10.5194/egusphere-2023-2172, https://doi.org/10.5194/egusphere-2023-2172, 2023
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Cooking activities can contribute substantially to indoor and ambient aerosol. We performed a comprehensive study with laboratory measurements cooking 19 different dishes and ambient measurements at two Christmas markets measuring various particle properties and trace gases of the emissions in real time. Similar emission characteristics were observed for dishes with the same preparation method, mainly due to similar cooking temperature and use of oil, with barbecues as especially strong source.
This article is included in the Encyclopedia of Geosciences
Shan Zhang, Lin Du, Zhaomin Yang, Narcisse Tsona Tchinda, Jianlong Li, and Kun Li
Atmos. Chem. Phys., 23, 10809–10822, https://doi.org/10.5194/acp-23-10809-2023, https://doi.org/10.5194/acp-23-10809-2023, 2023
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In this study, we have investigated the distinct impacts of humidity on the ozonolysis of two structurally different monoterpenes (limonene and Δ3-carene). We found that the molecular structure of precursors can largely influence the SOA formation under high RH by impacting the multi-generation reactions. Our results could advance knowledge on the roles of water content in aerosol formation and inform ongoing research on particle environmental effects and applications in models.
This article is included in the Encyclopedia of Geosciences
Yangzhihao Zhan, Min Xie, Wei Zhao, Tijian Wang, Da Gao, Pulong Chen, Jun Tian, Kuanguang Zhu, Shu Li, Bingliang Zhuang, Mengmeng Li, Yi Luo, and Runqi Zhao
Atmos. Chem. Phys., 23, 9837–9852, https://doi.org/10.5194/acp-23-9837-2023, https://doi.org/10.5194/acp-23-9837-2023, 2023
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Although the main source contribution of pollution is secondary inorganic aerosols in Nanjing, health risks mainly come from industry sources and vehicle emissions. Therefore, the development of megacities should pay more attention to the health burden of vehicle emissions, coal combustion, and industrial processes. This study provides new insight into assessing the relationship between source apportionment and health risks and can provide valuable insight into air pollution strategies.
This article is included in the Encyclopedia of Geosciences
Jonathan P. D. Abbatt and A. R. Ravishankara
Atmos. Chem. Phys., 23, 9765–9785, https://doi.org/10.5194/acp-23-9765-2023, https://doi.org/10.5194/acp-23-9765-2023, 2023
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With important climate and air quality impacts, atmospheric multiphase chemistry involves gas interactions with aerosol particles and cloud droplets. We summarize the status of the field and discuss potential directions for future growth. We highlight the importance of a molecular-level understanding of the chemistry, along with atmospheric field studies and modeling, and emphasize the necessity for atmospheric multiphase chemists to interact widely with scientists from neighboring disciplines.
This article is included in the Encyclopedia of Geosciences
Zhancong Liang, Zhihao Cheng, Ruifeng Zhang, Yiming Qin, and Chak K. Chan
Atmos. Chem. Phys., 23, 9585–9595, https://doi.org/10.5194/acp-23-9585-2023, https://doi.org/10.5194/acp-23-9585-2023, 2023
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In this study, we found that the photolysis of sodium nitrate leads to a much quicker decay of free amino acids (FAAs, with glycine as an example) in the particle phase than ammonium nitrate photolysis, which is likely due to the molecular interactions between FAAs and different nitrate salts. Since sodium nitrate likely co-exists with FAAs in the coarse-mode particles, particulate nitrate photolysis can possibly contribute to a rapid decay of FAAs and affect atmospheric nitrogen cycling.
This article is included in the Encyclopedia of Geosciences
Julian Resch, Kate Wolfer, Alexandre Barth, and Markus Kalberer
Atmos. Chem. Phys., 23, 9161–9171, https://doi.org/10.5194/acp-23-9161-2023, https://doi.org/10.5194/acp-23-9161-2023, 2023
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Detailed chemical analysis of organic aerosols is necessary to better understand their effects on climate and health. Aerosol samples are often stored for days to months before analysis. We examined the effects of storage conditions (i.e., time, temperature, and aerosol storage on filters or as solvent extracts) on composition and found significant changes in the concentration of individual compounds, indicating that sample storage can strongly affect the detailed chemical particle composition.
This article is included in the Encyclopedia of Geosciences
Xiaoliang Wang, Hatef Firouzkouhi, Judith C. Chow, John G. Watson, Warren Carter, and Alexandra S. M. De Vos
Atmos. Chem. Phys., 23, 8921–8937, https://doi.org/10.5194/acp-23-8921-2023, https://doi.org/10.5194/acp-23-8921-2023, 2023
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Open burning of household and municipal solid waste is a common practice in developing countries and is a significant source of air pollution. However, few studies have measured emissions from open burning of waste. This study determined gas and particulate emissions from open burning of 10 types of household solid-waste materials. These results can improve emission inventories, air quality management, and assessment of the health and climate effects of open burning of household waste.
This article is included in the Encyclopedia of Geosciences
Anita M. Avery, Mariam Fawaz, Leah R. Williams, Tami Bond, and Timothy B. Onasch
Atmos. Chem. Phys., 23, 8837–8854, https://doi.org/10.5194/acp-23-8837-2023, https://doi.org/10.5194/acp-23-8837-2023, 2023
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Pyrolysis is the thermal decomposition of fuels like wood which occurs during combustion or as an isolated process. During combustion, some pyrolysis products are emitted directly, while others are oxidized in the combustion process. This work describes the chemical composition of particle-phase pyrolysis products in order to investigate both the uncombusted emissions from wildfires and the fuel that participates in combustion.
This article is included in the Encyclopedia of Geosciences
Lan Ma, Reed Worland, Wenqing Jiang, Christopher Niedek, Chrystal Guzman, Keith J. Bein, Qi Zhang, and Cort Anastasio
Atmos. Chem. Phys., 23, 8805–8821, https://doi.org/10.5194/acp-23-8805-2023, https://doi.org/10.5194/acp-23-8805-2023, 2023
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Although photooxidants are important in airborne particles, little is known of their concentrations. By measuring oxidants in a series of particle dilutions, we predict their concentrations in aerosol liquid water (ALW). We find •OH concentrations in ALW are on the order of 10−15 M, similar to their cloud/fog values, while oxidizing triplet excited states and singlet molecular oxygen have ALW values of ca. 10−13 M and 10−12 M, respectively, roughly 10–100 times higher than in cloud/fog drops.
This article is included in the Encyclopedia of Geosciences
Daniel A. Knopf, Peiwen Wang, Benny Wong, Jay M. Tomlin, Daniel P. Veghte, Nurun N. Lata, Swarup China, Alexander Laskin, Ryan C. Moffet, Josephine Y. Aller, Matthew A. Marcus, and Jian Wang
Atmos. Chem. Phys., 23, 8659–8681, https://doi.org/10.5194/acp-23-8659-2023, https://doi.org/10.5194/acp-23-8659-2023, 2023
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Ambient particle populations and associated ice-nucleating particles (INPs)
were examined from particle samples collected on board aircraft in the marine
boundary layer and free troposphere in the eastern North Atlantic during
summer and winter. Chemical imaging shows distinct differences in the
particle populations seasonally and with sampling altitudes, which are
reflected in the INP types. Freezing parameterizations are derived for
implementation in cloud-resolving and climate models.
This article is included in the Encyclopedia of Geosciences
Dandan Liu, Yun Zhang, Shujun Zhong, Shuang Chen, Qiaorong Xie, Donghuan Zhang, Qiang Zhang, Wei Hu, Junjun Deng, Libin Wu, Chao Ma, Haijie Tong, and Pingqing Fu
Atmos. Chem. Phys., 23, 8383–8402, https://doi.org/10.5194/acp-23-8383-2023, https://doi.org/10.5194/acp-23-8383-2023, 2023
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Based on ultra-high-resolution mass spectrometry analysis, we found that β-pinene oxidation-derived highly oxygenated organic molecules (HOMs) exhibit higher yield at high ozone concentration, while limonene oxidation-derived HOMs exhibit higher yield at moderate ozone concentration. The distinct molecular response of HOMs and low-volatile species in different biogenic secondary organic aerosols to ozone concentrations provides a new clue for more accurate air quality prediction and management.
This article is included in the Encyclopedia of Geosciences
Mengying Bao, Yan-Lin Zhang, Fang Cao, Yihang Hong, Yu-Chi Lin, Mingyuan Yu, Hongxing Jiang, Zhineng Cheng, Rongshuang Xu, and Xiaoying Yang
Atmos. Chem. Phys., 23, 8305–8324, https://doi.org/10.5194/acp-23-8305-2023, https://doi.org/10.5194/acp-23-8305-2023, 2023
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The interaction between the sources and molecular compositions of humic-like substances (HULIS) at Nanjing, China, was explored. Significant fossil fuel source contributions to HULIS were found in the 14C results from biomass burnng and traffic emissions. Increasing biogenic secondary organic aerosol (SOA) products and anthropogenic aromatic compounds were detected in summer and winter, respectively.
This article is included in the Encyclopedia of Geosciences
Molly Frauenheim, Jason D. Surratt, Zhenfa Zhang, and Avram Gold
Atmos. Chem. Phys., 23, 7859–7866, https://doi.org/10.5194/acp-23-7859-2023, https://doi.org/10.5194/acp-23-7859-2023, 2023
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We report synthesis of the isoprene-derived photochemical oxidation products trans- and cis-β-epoxydiols in high overall yields from inexpensive, readily available starting compounds. Protection/deprotection steps or time-consuming purification is not required, and the reactions can be scaled up to gram quantities. The procedures provide accessibility of these important compounds to atmospheric chemistry laboratories with only basic capabilities in organic synthesis.
This article is included in the Encyclopedia of Geosciences
Xiangyun Zhang, Jun Li, Sanyuan Zhu, Junwen Liu, Ping Ding, Shutao Gao, Chongguo Tian, Yingjun Chen, Ping'an Peng, and Gan Zhang
Atmos. Chem. Phys., 23, 7495–7502, https://doi.org/10.5194/acp-23-7495-2023, https://doi.org/10.5194/acp-23-7495-2023, 2023
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The results show that 14C elemental carbon (EC) was not only related to the isolation method but also to the types and proportions of the biomass sources in the sample. The hydropyrolysis (Hypy) method, which can be used to isolate a highly stable portion of ECHypy and avoid charring, is a more effective and stable approach for the matrix-independent 14C quantification of EC in aerosols, and the 13C–ECHypy and non-fossil ECHypy values of SRM1649b were –24.9 ‰ and 11 %, respectively.
This article is included in the Encyclopedia of Geosciences
Amir Yazdani, Satoshi Takahama, John K. Kodros, Marco Paglione, Mauro Masiol, Stefania Squizzato, Kalliopi Florou, Christos Kaltsonoudis, Spiro D. Jorga, Spyros N. Pandis, and Athanasios Nenes
Atmos. Chem. Phys., 23, 7461–7477, https://doi.org/10.5194/acp-23-7461-2023, https://doi.org/10.5194/acp-23-7461-2023, 2023
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Organic aerosols directly emitted from wood and pellet stove combustion are found to chemically transform (approximately 15 %–35 % by mass) under daytime aging conditions simulated in an environmental chamber. A new marker for lignin-like compounds is found to degrade at a different rate than previously identified biomass burning markers and can potentially provide indication of aging time in ambient samples.
This article is included in the Encyclopedia of Geosciences
Hao Luo, Luc Vereecken, Hongru Shen, Sungah Kang, Iida Pullinen, Mattias Hallquist, Hendrik Fuchs, Andreas Wahner, Astrid Kiendler-Scharr, Thomas F. Mentel, and Defeng Zhao
Atmos. Chem. Phys., 23, 7297–7319, https://doi.org/10.5194/acp-23-7297-2023, https://doi.org/10.5194/acp-23-7297-2023, 2023
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Oxidation of limonene, an element emitted by trees and chemical products, by OH, a daytime oxidant, forms many highly oxygenated organic molecules (HOMs), including C10-20 compounds. HOMs play an important role in new particle formation and growth. HOM formation can be explained by the chemistry of peroxy radicals. We found that a minor branching ratio initial pathway plays an unexpected, significant role. Considering this pathway enables accurate simulations of HOMs and other concentrations.
This article is included in the Encyclopedia of Geosciences
Heather L. Runberg and Brian J. Majestic
Atmos. Chem. Phys., 23, 7213–7223, https://doi.org/10.5194/acp-23-7213-2023, https://doi.org/10.5194/acp-23-7213-2023, 2023
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Environmentally persistent free radicals (EPFRs) are an emerging pollutant found in soot particles. Understanding how these change as they move through the atmosphere is important to human health. Here, soot was generated in the laboratory and exposed to simulated sunlight. The concentrations and characteristics of EPFRs in the soot were measured and found to be unchanged. However, it was also found that the ability of soot to form hydroxyl radicals was stronger for fresh soot.
This article is included in the Encyclopedia of Geosciences
Wenqing Jiang, Christopher Niedek, Cort Anastasio, and Qi Zhang
Atmos. Chem. Phys., 23, 7103–7120, https://doi.org/10.5194/acp-23-7103-2023, https://doi.org/10.5194/acp-23-7103-2023, 2023
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We studied how aqueous-phase secondary organic aerosol (aqSOA) form and evolve from a phenolic carbonyl commonly present in biomass burning smoke. The composition and optical properties of the aqSOA are significantly affected by photochemical reactions and are dependent on the oxidants' concentration and identity in water. During photoaging, the aqSOA initially becomes darker, but prolonged aging leads to the formation of volatile products, resulting in significant mass loss and photobleaching.
This article is included in the Encyclopedia of Geosciences
Cited articles
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, 12, 4478–4485, 2008.
Altieri, K., Carlton, A. G., Lim, H., Turpin, B. J., and Seitzinger, S. P.: Evidence for oligomer formation in clouds: Reaction of isoprene oxidation products, Environ. Sci. Technol., 40,4956–4960, 2006.
Altieri, K. E., Seitzinger, S. P., Carlton, A. G., Turpin, B. J., Klein, G. C., and Marshall, A. G.: Oligomers formed through in-cloud methylglyoxal reactions: Chemical composition, properties, and mechanisms investigated by ultra-high resolution FT-ICR mass spectrometry, Atmos. Environ., 42,1476–1490, 2008.
Altieri, K. E., Turpin, B. J., and Seitzinger, S. P.: Oligomers, organosulfates, and nitrooxy organosulfates in rainwater identified by ultra-high resolution electrospray ionization FT-ICR mass spectrometry, Atmos. Chem. Phys., 9, 2533–2542, https://doi.org/10.5194/acp-9-2533-2009, 2009.
Anastasio, C., Faust, B. C., and Rao, C. J.: Aromatic Carbonyl Compounds as Aqueous Phase Photochemical Sources of Hydrogen Peroxide in Acidic Sulfate Aerosols, Fogs, and Clouds. 1. Non-Phenolic Methoxybenzaldehydes and Methoxyacetophenones with Reductants (Phenols), Environ. Sci. Technol., 31, 218–232, 1997.
Arakaki, T. and Faust, B. C.: Sources, sinks and mechanisms of hydroxyl radical (OH) photoproduction and consumption in authentic acidic continental cloud waters from Whiteface mountain, New York: The role of the Fe(r) (r = II, III) photochemical cycle, J. Geophys. Res., 103, 3487–3504, 1998.
Arellanes, C., Paulson, S. E., Fine, P. M., and Sioutas, C.: Exceeding of Henry's Law by Hydrogen Peroxide Associated with Urban Aerosols, Environ. Sci. Technol., 40, 4859–4866, https://doi.org/10.1021/es0513786, 2006.
Baboukas, E. D., Kanakidou, M., and Mihalopoulos, N.: Carboxylic acids in gas and particulate phase above the Atlantic Ocean, J. Geophys. Res., 105,14459–14471, 2000.
Bahreini, R., Ervens, B., Middlebrook, A. M., Warneke, C., DeGouw, J. A., DeCarlo, P., Jimenez, J. L., Brock, C. A., Neuman, J. A., Ryerson, T. B., Stark, H., Atlas, E., Brioude, J., Fried, A., Holloway, J. S., Peischl, J., Richter, D., Walega, J., Weibring, P., Wollny, A. G., and Fehsenfeld, F. C.: Organic aerosol formation in urban and industrial plumes in Houston, TX, J. Geophys. Res., 114, D00F16, https://doi.org/10.1029/2008JD011493, 2009.
Barsanti, K. C. and Pankow, J. F.: Thermodynamics of the formation of atmospheric organic particulate matter by accretion reactions - Part 1: aldehydes and ketones, Atmos. Environ, 38, 4371–4382, 2004.
Barsanti, K. C. and Pankow, J. F.: Thermodynamics of the formation of atmospheric organic particulate matter by accretion reactions - Part 2: Dialdehydes, methylglyoxal, and diketones, Atmos. Environ., 39, 6597–6607, 2005.
Bateman, A. P., Nizkorodov, S. A., Laskin, J., and Laskin, A.: Photolytic processing of secondary organic aerosols dissolved in cloud droplets, Phys. Chem. Chem. Phys., 13, 12199–12212, 2011.
Bertram, A. K., Martin, S. T., Hanna, S. J., Smith, M. L., Bodsworth, A., Chen, Q., Kuwata, M., Liu, A., You, Y., and Zorn, S. R.: Predicting the relative humidities of liquid-liquid phase separation, efflorescence, and deliquescence of mixed particles of ammonium sulfate, organic material, and water using the organic-to-sulfate mass ratio of the particle and the oxygen-to-carbon elemental ratio of the organic component, Atmos. Chem. Phys., 11, 10995–11006, https://doi.org/10.5194/acp-11-10995-2011, 2011.
Blando, J. D. and Turpin, B. J.: Secondary organic aerosol formation in cloud and fog droplets: a literature evaluation of plausibilty, Atmos. Environ., 34, 1623–1632, 2000.
Blando, J. D., Porcja, R. J., Li, T., Bowman, D., Lioy, P. J., and Turpin, B. J.: Secondary Formation and the Smoky Mountain Organic Aerosol: An Examination of Aerosol Polarity and Functional Group Composition During SEAVS, Environ. Sci. Technol, 32, 604–613, 1998.
Buxton, G. V., Malone, T. N., and Salmon, G. A.: Oxidation of glyoxal initiated by OH in oxygenated aqueous solutions, J. Chem. Soc. Faraday Trans., 93, 2889–2891, 1997.
Cappa, C., Che, D., Kessler, S., Kroll, J., and Wilson, K.: Variations in organic aerosol optical and hygroscopic properties upon heterogeneous OH oxidation, J. Geophys. Res., 116, D15204, https://doi.org/10.1029/2011jd015918, 2011.
Carbone, C., Decesari, S., Mircea, M., Giulianelli, L., Finessi, E., Rinaldi, M., Fuzzi, S., Marinoni, A., Duchi, R., Perrino, C., Sargolini, T., Vardè, M., Sprovieri, F., Gobbi, G. P., Angelini, F., and Facchini, M. C.: Size-resolved aerosol chemical composition over the Italian Peninsula during typical summer and winter conditions, Atmos. Environ., 44, 5269–5278, https://doi.org/10.1016/j.atmosenv.2010.08.008, 2010.
Carlton, A. G., Turpin, B. J., Lim, H., Altieri, K. E., and Seitzinger, S.: Link between isoprene and secondary organic aerosol (SOA): Pyruvic acid oxidation yields low volatility organic acid in clouds, Geophys. Res. Lett., 33, 06822, https://doi.org/10.1029/2005GL025374, 2006.
Carlton, A. G., Turpin, B. J., Altieri, K. E., Reff, A., Seitzinger, S., Lim, H., and Ervens, B.: Atmospheric oxalic acid and SOA production from glyoxal: Results of aqueous photooxidation experiments, Atmos. Environ., 41, 7588–7602, 2007.
Carlton, A. G., Turpin, B. J., Altieri, K. E., Seitzinger, S. P., Mathur, R., Roselle, S. J., and Weber, R. J.: CMAQ Model Performance Enhanced When In-Cloud Secondary Organic Aerosol is Included: Comparisons of Organic Carbon Predictions with Measurements, Environ. Sci. Technol., 42, 8789–8802, 2008.
Carlton, A. G., Pinder, R. W., Bhave, P. V., and Pouliot, G. A.: To What Extent Can Biogenic SOA be Controlled?, Environ. Sci. Technol., 44, 3376–3380, https://doi.org/10.1021/es903506b, 2010.
Casale, M. T., Richman, A. R., Elrod, M. J., Garland, R. M., Beaver, M. R., and Tolbert, M. A.: Kinetics of acid-catalyzed aldol condensation reactions of aliphatic aldehydes, Atmos. Environ., 41, 6212–6224, 2007.
Chang, J. L. and Thompson, J. E.: Characterization of colored products formed during irradiation of aqueous solutions containing H2O2 and phenolic compounds, Atmos. Environ., 44, 541–551, https://doi.org/10.1016/j.atmosenv.2009.10.042, 2010.
Chang, W. L., Griffin, R. J., and Dabdub, D.: Partitioning phase preference for secondary organic aerosol in an urban atmosphere, P. Natl. Acad. Sci., 107, 6705–6710, https://doi.org/10.1073/pnas.0911244107, 2010.
Chen, J., Griffin, R. J., Grini, A., and Tulet, P.: Modeling secondary organic aerosol formation through cloud processing of organic compounds, Atmos. Chem. Phys., 7, 5343–5355, https://doi.org/10.5194/acp-7-5343-2007, 2007.
Chen, Z. M., Wang, H. L., Zhu, L. H., Wang, C. X., Jie, C. Y., and Hua, W.: Aqueous-phase ozonolysis of methacrolein and methyl vinyl ketone: a potentially important source of atmospheric aqueous oxidants, Atmos. Chem. Phys., 8, 2255–2265, https://doi.org/10.5194/acp-8-2255-2008, 2008.
Cocker III, D. R., Clegg, S. L., Flagan, R. L., and Seinfeld, J. H.: The effect of water on gas-particle partitioning of secondary organic aerosol. Part I: a-pinene/ozone system, Atmos. Environ., 35, 6049–6072, 2001a.
Cocker III, D. R., Mader, B. T., Kalberer, M., Flagan, R. L., and Seinfeld, J. H.: The effect of water on gas-particle partitioning of secondary organic aerosol. Part II: m-xylene and 1,3,5-trimethyl benzene photoxidation systems, Atmos. Environ., 35, 6073–6085, 2001b.
Compernolle, S., Ceulemans, K., and Müller, J.-F.: EVAPORATION: a new vapour pressure estimation methodfor organic molecules including non-additivity and intramolecular interactions, Atmos. Chem. Phys., 11, 9431–9450, https://doi.org/10.5194/acp-11-9431-2011, 2011.
Couvidat, F. and Seigneur, C.: Modeling secondary organic aerosol formation from isoprene oxidation under dry and humid conditions, Atmos. Chem. Phys., 11, 893–909, https://doi.org/10.5194/acp-11-893-2011, 2011.
Crahan, K. K., Hegg, D., Covert, D. S., and Jonsson, H.: An exploration of aqueous oxalic acid production in the coastal marine atmosphere, Atmos. Environ., 38, 3757–3764, 2004.
Creighton, D. J., Migliorini, M., Pourmotabbed, T., and Guha, M. K.: Optimization of efficieny in the glyoxylase pathway, Biochem., 27, 7376–7384, 1988.
Day, M. C. and Pandis, S. N.: Predicted changes in summertime organic aerosol concentrations due to increased temperatures, Atmos. Environ., 45, 6546–6556, https://doi.org/10.1016/j.atmosenv.2011.08.028, 2011.
De Haan, D. O., Corrigan, A. L., Smith, K. W., Stroik, D. R., Turley, J. J., Lee, F. E., Tolbert, M. A., Jimenez, J. L., Cordova, K. E., and Ferrell, G. R.: Secondary organic aerosol-forming reactions of glyoxal with amino acids, Environ. Sci. Technol., 43, 2818–2824, 2009a.
De Haan, D. O., Corrigan, A. L., Tolbert, M. A., Jimenez, J. L., Wood, S. E., and Turley, J. J.: Secondary Organic Aerosol Formation by Self-Reactions of Methylglyoxal and Glyoxal in Evaporating Droplets, Environ. Sci Technol., 43, 8184–8190, https://doi.org/10.1021/es902152t, 2009b.
De Haan, D. O., Tolbert, M. A., and Jimenez, J. L.: Atmospheric condensed phase reactions of glyoxal with methylamine, Geophys. Res. Lett., 36, L11819, https://doi.org/10.1029/2009GL037441, 2009c.
De Haan, D. O., Hawkins, L. N., Kononenko, J. A., Turley, J. J., Corrigan, A. L., Tolbert, M. A., and Jimenez, J. L.: Formation of Nitrogen-Containing Oligomers by Methylglyoxal and Amines in Simulated Evaporating Cloud Droplets, Environ. Sci. Tech., 45, 984–991, https://doi.org/10.1021/es102933x, 2010.
Debus, H.: Über die Einwirkung des Ammoniaks auf Glyoxal, Annalen der Chemie und Pharmacie, 107, 199–208, https://doi.org/10.1002/jlac.18581070209, 1858.
DeGouw, J. A., Middlebrook, A. M., Warneke, C., Goldan, P. D., Kuster, W. C., Roberts, J. M., Fehsenfeld, F. C., Worsnop, D. R., Canagaratna, M. R., Pszenny, A. A. P., Keene, W. C., Marchewka, M., Bertram, S. B., and Bates, T. S.: Budget of organic carbon in a polluted atmosphere: Results from the New England Air Quality Study in 2002, J. Geophys. Res., 110, D16305, https://doi.org/10.1029/2004JD005623, 2005.
Dixon, R. W. and Aasen, H.: Measurement of hydroxymethanesulfonate in atmospheric aerosols, Atmos. Environ., 33, 2023–2029, 1999.
Donahue, N. M., Robinson, A. L., Stanier, C. O., and Pandis, S. N.: Coupled partitioning, dilution and chemical aging of semivolatile organics, Environ. Sci. Technol., 40, 2635–2643, 2006.
Edney, E. O., Kleindienst, T. E., Jaoui, M., Lewandowski, M., Offenberg, J. H., Wang, W., and Claeys, M.: Formation of 2-methyl tetrols and 2-methylglyceric acid in secondary organic aerosol from laboratory irradiated isoprene/NOx/SO2/air mixtures and their detection in ambient PM2.5 samples collected in the eastern United States, Atmos. Environ., 39, 5281–5289, 2005.
El Haddad, I., Yao Liu, Nieto-Gligorovski, L., Michaud, V., Temime-Roussel, B., Quivet, E., Marchand, N., Sellegri, K., and Monod, A.: In-cloud processes of methacrolein under simulated conditions – Part 2: Formation of secondary organic aerosol, Atmos. Chem. Phys., 9, 5107–5117, https://doi.org/10.5194/acp-9-5107-2009, 2009.
Ervens, B. and Volkamer, R.: Glyoxal processing by aerosol multiphase chemistry: towards a kinetic modeling framework of secondary organic aerosol formation in aqueous particles, Atmos. Chem. Phys., 10, 8219–8244, https://doi.org/10.5194/acp-10-8219-2010, 2010.
Ervens, B., George, C., Williams, J. E., Buxton, G. V., Salmon, G. A., Bydder, M., Wilkinson, F., Dentener, F., Mirabel, P., Wolke, R., and Herrmann, H.: CAPRAM2.4 (MODAC mechanism): An extended and condensed tropospheric aqueous phase mechanism and its application, J. Geophys. Res., 108, 4426, https://doi.org/10.1029/2002JD002202, 2003a.
Ervens, B., Gligorovski, S., and Herrmann, H.: Temperature dependent rate constants for hydroxyl radical reactions with organic compounds in aqueous solution, Phys. Chem. Chem. Phys., 5, 1811–1824, 2003b.
Ervens, B., Feingold, G., Frost, G. J., and Kreidenweis, S. M.: A modeling study of aqueous production of dicarboxylic acids, 1. Chemical pathways and speciated organic mass production, J. Geophys. Res., 109, D15205, https://doi.org/10.1029/2003JD004387, 2004.
Ervens, B., Feingold, G., and Kreidenweis, S. M.: The influence of water-soluble organic carbon on cloud drop number concentration, J. Geophys. Res., 110, D18211, https://doi.org/10.1029/2004JD005634, 2005.
Ervens, B. and Kreidenweis, S. M.: SOA formation by biogenic and carbonyl compounds: Data evaluation and application, Environ. Sci. Technol., 41, 3904–3910, 2007.
Ervens, B., Carlton, A. G., Turpin, B. J., Altieri, K. E., Kreidenweis, S. M., and Feingold, G.: Secondary organic aerosol yields from cloud-processing of isoprene oxidation products, Geophys. Res. Lett., 35, L02816, https://doi.org/10.1029/2007gl031828, 2008.
Ervens, B., Cubison, M. J., Andrews, E., Feingold, G., Ogren, J. A., Jimenez, J. L., Quinn, P. K., Bates, T. S., Wang, J., Zhang, Q., Coe, H., Flynn, M., and Allan, J. D.: CCN predictions using simplified assumptions of organic aerosol composition and mixing state: a synthesis from six different locations, Atmos. Chem. Phys., 10, 4795–4807, https://doi.org/10.5194/acp-10-4795-2010, 2010.
Fast, J. D., de Foy, B., Acevedo Rosas, F., Caetano, E., Carmichael, G., Emmons, L., McKenna, D., Mena, M., Skamarock, W., Tie, X., Coulter, R. L., Barnard, J. C., Wiedinmyer, C., and Madronich, S.: A meteorological overview of the MILAGRO field campaigns, Atmos. Chem. Phys., 7, 2233–2257, https://doi.org/10.5194/acp-7-2233-2007, 2007.
Favez, O., Sciare, J., Cachier, H., Alfaro, S. C., and Abdelwahab, M. M.: Significant formation of water-insoluble secondary organic aerosols in semi-arid urban environment, Geophys. Res. Lett., 35, L15801, https://doi.org/10.1029/2008gl034446, 2008.
Feingold, G.: Modeling of the first indirect effect: Analysis of measurement requirements, Geophys. Res. Lett., 30, 1997, https://doi.org/10.1029/2003GL017967, 2003.
Feingold, G. and Kreidenweis, S.: Does cloud processing of aerosol enhance droplet concentrations?, J. Geophys. Res., 105, 24351–24361, 2000.
Fillo, J. D., Koehler, C. A., Nguyen, T. P., DeHaan, D. O., Gilbert, B. A., and Flinn, K. P.: Simulating Secondary Organic Aerosol Activation by Condensation of Multiple Organics on Seed Particles, Environ. Sci. Technol., 37, 4672–4677, 2003.
Froyd, K. D., Murphy, S. M., Murphy, D. M., deGouw, J. A., Eddingsaas, N. C., and Wennberg, P. O.: Contribution of isoprene-derived organosulfates to free tropospheric aerosol mass, P. Natl. Acad. Sci., 108, 21360–21365, https://doi.org/10.1073/pnas.1012561107, 2010.
Fu, T., Jacob, D. J., Wittrock, F., Burrows, J. P., Vrekoussis, M., and Henze, D. K.: Global budgets of atmospheric glyoxal, methylglyoxal, and implications for formation of secondary organic aerosol, J. Geophys. Res., 113, D15303, https://doi.org/10.1029/2007JD009505, 2008.
Fu, T., Jacob, D. J., and Heald, C. L.: Aqueous-phase reactive uptake of dicarbonyls as a source of organic aerosol over eastern North America, Atmos. Environ., 43, 1814–1822, 2009.
Furukawa, T. and Takahashi, Y.: Oxalate metal complexes in aerosol particles: implications for the hygroscopicity of oxalate-containing particles, Atmos. Chem. Phys., 11, 4289–4301, https://doi.org/10.5194/acp-11-4289-2011, 2011.
Fuzzi, S., Decesari, S., Facchini, M. C., Matta, E., Mircea, M., and Tagliavini, E.: A simplified model of the water soluble organic component of atmospheric aerosol, Geophys. Res. Lett., 28, 4079–4082, 2001.
Fuzzi, S., Facchini, M. C., Decesari, S., Matta, E., and Mircea, M.: Soluble organic compounds in fog and cloud droplets: What have we learned over the past few years?, Atmos. Res., 64, 89–98, 2002.
Galloway, M. M., Chhabra, P. S., Chan, A. W. H., Surratt, J. D., Flagan, R. C., Seinfeld, J. H., and Keutsch, F. N.: Glyoxal uptake on ammonium sulphate seed aerosol: reaction products and reversibility of uptake under dark and irradiated conditions, Atmos. Chem. Phys., 9, 3331–3345, https://doi.org/10.5194/acp-9-3331-2009, 2009.
Galloway, M. M., Huisman, A. J., Yee, L. D., Chan, A. W. H., Loza, C. L., Seinfeld, J. H., and Keutsch, F. N.: Yields of oxidized volatile organic compounds during the OH radical initiated oxidation of isoprene, methyl vinyl ketone, and methacrolein under high-NOx conditions, Atmos. Chem. Phys. Discuss., 11, 10693–10720, http://dx.doi.org/10.5194/acpd-11-10693-2011https://doi.org/10.5194/acpd-11-10693-2011, 2011a.
Galloway, M. M., Loza, C. L., Chhabra, P. S., Chan, A. W. H., Yee, L. D., Seinfeld, J. H., and Keutsch, F. N.: Analysis of photochemical and dark glyoxal uptake: Implications for SOA formation, Geophys. Res. Lett., 38, L17811, https://doi.org/10.1029/2011gl048514, 2011b.
Gelencser, A., Hoffer, A., Kiss, G., Tombasz, E., Kurdi, R., and Bencze, L.: In-situ formation of Light-Absorbing Organic Matter in Cloud Water, J. Atmos. Chem., 45, 25–33, 2003.
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.
Graedel, T. E. and Weschler, C. J.: Chemistry Within Aqueous Atmospheric Aerosols and Raindrops, Rev. Geophys. Space Phys., 19, 505–539, 1981.
Grgic, I., Nieto-Gligorovski, L. I., Net, S., Temime-Roussel, B., Gligorovski, S., and Wortham, H.: Light induced multiphase chemistry of gas-phase ozone on aqueous pyruvic and oxalic acids, Phys. Chem. Chem. Phys., 12, 698–707, 2010.
Griffin, R. J., Nguyen, K., Dabdub, D., and Seinfeld, J. H.: A coupled Hydrophobic-Hydrophilic Model for Predicting Secondary Aerosol Formation, J. Atmos. Chem., 44, 171–190, 2003.
Guzman, M. I., Colussi, A. J., and Hoffmann, M. R.: Photoinduced oligomerization of aqueous pyruvic acid, J. Phys. Chem. A, 110, 3619–3626, 2006.
Hasson, A. S. and Paulson, S. E.: An investigation of the relationship between gas-phase and aerosol borne hydroperoxides in urban air, J. Aerosol Sci., 34, 459–468, 2003.
Hatch, L. E., Creamean, J. M., Ault, A. P., Surratt, J. D., Chan, M. N., Seinfeld, J. H., Edgerton, E. S., Su, Y., and Prather, K. A.: Measurements of Isoprene-Derived Organosulfates in Ambient Aerosols by Aerosol Time-of-Flight Mass Spectrometry – Part 1: Single Particle Atmospheric Observations in Atlanta, Environ. Sci. Technol., 45, 5105–5111, https://doi.org/10.1021/es103944a, 2011.
Heald, C. L., Jacob, D. J., Park, R. J., Russell, L. M., Huebert, B. J., Seinfeld, J. H., Liao, H., and Weber, R. J.: A large organic aerosol source in the free troposphere missing from current models, Geophys. Res. Lett., 32, L18809, https://doi.org/10.1029/2005GL023831, 2005.
Heald, C. L., Jacob, D. J., Turquety, S., Hudman, R. C., Weber, R. J., Sullivan, A. P., Peltier, R. E., Atlas, E. L., deGouw, J. A., Warneke, C., Holloway, J. S., Newman, J. A., Flocke, F. M., and Seinfeld, J. H.: Concentrations and sources of organic carbon aerosols in the free troposphere over North America, J. Geophys. Res., 111, D23S47, https://doi.org/10.1029/2006JD007705, 2006.
Heald, C. L., Coe, H., Jimenez, J. L., Weber, R. J., Bahreini, R., Middlebrook, A. M., Russell, L. M., Jolleys, M., Fu, T.-M., Allan, J. D., Bower, K. N., Capes, G., Crosier, J., Morgan, W. T., Robinson, N. H., Williams, P. I., Cubison, M. J., DeCarlo, P. F., and Dunlea, E. J.: Exploring the vertical profile of atmospheric organic aerosol: comparing 17 aircraft field campaigns with a global model, Atmos. Chem. Phys. Discuss., 11, 25371–25425, https://doi.org/10.5194/acpd-11-25371-2011, 2011.
Healy, R. M., Wenger, J. C., Metzger, A., Duplissy, J., Kalberer, M., and Dommen, J.: Gas/particle partitioning of carbonyls in the photooxidation of isoprene and 1,3,5-trimethylbenzene, Atmos. Chem. Phys., 8, 3215–3230, https://doi.org/10.5194/acp-8-3215-2008, 2008.
Healy, R. M., Temime, B., Kuprovskyte, K., and Wenger, J. C.: Effect of Relative Humidity on Gas/Particle Partitioning and Aerosol Mass Yield in the Photooxidation of p-Xylene, Environ. Sci. Tech., 43, 1884–1889, https://doi.org/10.1021/es802404z, 2009.
Hecobian, A., Zhang, X., Zheng, M., Frank, N., Edgerton, E. S., and Weber, R. J.: Water-Soluble Organic Aerosol material and the light-absorption characteristics of aqueous extracts measured over the Southeastern United States, Atmos. Chem. Phys., 10, 5965–5977, https://doi.org/10.5194/acp-10-5965-2010, 2010.
Hennigan, C. J., Sullivan, A. P., Fountoukis, C. I., Nenes, A., Hecobian, A., Vargas, O., Peltier, R. E., Case Hanks, A. T., Huey, L. G., Lefer, B. L., Russell, A. G., and Weber, R. J.: On the volatility and production mechanisms of newly formed nitrate and water soluble organic aerosol in Mexico City, Atmos. Chem. Phys., 8, 3761–3768, https://doi.org/10.5194/acp-8-3761-2008, 2008a.
Hennigan, C. J., Bergin, M. H., Dibb, J. E., and Weber, R. J.: Enhanced secondary organic aerosol formation due to water uptake by fine particles, Geophys. Res. Lett, 35, L18801, https://doi.org/10.1029/2008GL035046, 2008b.
Hennigan, C. J., Bergin, M. H., and Weber, R. J.: Correlations between water-soluble organic aerosol and water vapor: a synergistic effect from biogenic emissions?, Environ. Sci Technol., 42, 9079–9085, 2008c.
Hennigan, C. J., Bergin, M. H., Russell, A. G., Nenes, A., and Weber, R. J.: Gas/particle partitioning of water-soluble organic aerosol in Atlanta, Atmos. Chem. Phys., 9, 3613–3628, https://doi.org/10.5194/acp-9-3613-2009, 2009.
Henze, D. K. and Seinfeld, J. H.: Global secondary organic aerosol from isoprene oxidation, Geophys. Res. Lett., 33, L09812, https://doi.org/10.1029/2006GL025976, 2006.
Herckes, P., Lee, T., Trenary, L., Kang, G., Chang, H., and Collett, J. L.: Organic Matter in Central California Radiation Fogs, Environ. Sci. Technol., 36, 4777–4782, https://doi.org/10.1021/es025889t, 2002.
Herckes, P., Chang, H., Lee, T., and Collett Jr., J. L.: Air pollution processing by radiation fogs, Water Air Soil Pollut., 181, 65–75, 2007.
Hering, S. V. and Friedlander, S. K.: Origins of Sulfur Size Distributions in the Los Angeles Basin, Atmos. Environ., 16, 2647–2656, 1982.
Herrmann, H.: Kinetics of aqueous phase reactions relevant for atmospheric chemistry, Chem. Rev., 103, 4691–4716, 2003.
Herrmann, H., Ervens, B., Jacobi, H.-W., Wolke, R., Nowacki, P., and Zellner, R.: CAPRAM2.3: A Chemical Aqueous Phase Radical Mechanism for Tropospheric Chemistry, J. Atmos. Chem., 36, 231–284, 2000.
Herrmann, H., Tilgner, A., Barzaghi, P., Majdik, Z., Gligorovski, S., Poulain, L., and Monod, A.: Towards a more detailed description of tropospheric aqueous phase organic chemistry: CAPRAM 3.0, Atmos. Environ, 39, 4351–4363, 2005.
Herrmann, H., Hoffmann, D., Schaefer, T., Bräuer, P., and Tilgner, A.: Tropospheric Aqueous-Phase Free-Radical Chemistry: Radical Sources, Spectra, Reaction Kinetics and Prediction Tools, Chem. Phys. Chem., 11, 3796–3822, https://doi.org/10.1002/cphc.201000533, 2010.
Hersey, S. P., Craven, J. S., Schilling, K. A., Metcalf, A. R., Sorooshian, A., Chan, M. N., Flagan, R. C., and Seinfeld, J. H.: The Pasadena Aerosol Characterization Observatory (PACO): chemical and physical analysis of the Western Los Angeles basin aerosol, Atmos. Chem. Phys., 11, 7417–7443, https://doi.org/10.5194/acp-11-7417-2011, 2011.
Hodzic, A., Jimenez, J. L., Madronich, S., Canagaratna, M. R., DeCarlo, P. F., Kleinman, L., and Fast, J.: Modeling organic aerosols in a megacity: potential contribution of semi-volatile and intermediate volatility primary organic compounds to secondary organic aerosol formation, Atmos. Chem. Phys., 10, 5491–5514, https://doi.org/10.5194/acp-10-5491-2010, 2010.
Hoffer, A., Kiss, G., Blazsó, M., and Gelencsér, A.: Chemical characterization of humic-like substances (HULIS) formed from a lignin-type precursor in model cloud water, Geophys. Res. Lett., 31, L06115, https://doi.org/10.1029/2003gl018962, 2004.
Hoppel, W. A., Frick, G. M., Fitzgerald, J. W., and Larson, R. E.: Marine Boundary layer measurements of new particle formation and the effects nonprecipitating clouds have on aerosol size distribution, J. Geophys. Res., 99, 14443–14459, 1994.
Hoyle, C. R., Boy, M., Donahue, N. M., Fry, J. L., Glasius, M., Guenther, A., Hallar, A. G., Huff Hartz, K., Petters, M. D., Petäjä, T., Rosenoern, T., and Sullivan, A. P.: A review of the anthropogenic influence on biogenic secondary organic aerosol, Atmos. Chem. Phys., 11, 321–343, https://doi.org/10.5194/acp-11-321-2011, 2011.
Huang, D., Zhang, X., Chen, Z. M., Zhao, Y., and Shen, X. L.: The kinetics and mechanism of an aqueous phase isoprene reaction with hydroxyl radical, Atmos. Chem. Phys., 11, 7399–7415, https://doi.org/10.5194/acp-11-7399-2011, 2011.
Huang, X.-F., Yu, J. Z., He, L.-Y., and Yuan, Z.: Water-soluble organic carbon and oxalate in aerosols at a coastal urban site in China: Size distribution characteristics, sources, and formation mechanisms, J. Geophys. Res., 111, D22212, https://doi.org/10.1029/2006jd007408, 2006.
Huang, X. H. H., Ip, H. S. S., and Yu, J. Z.: Secondary organic aerosol formation from ethylene in the urban atmosphere of Hong Kong: A multiphase chemical modeling study, J. Geophys. Res., 116, D03206, https://doi.org/10.1029/2010jd014121, 2011.
Igawa, M., Munger, J. W., and Hoffmann, M. R.: Analysis of aldehydes in cloud- and fogwater samples by HPLC with a postcolumn reaction detector, Environ. Sci. Technol, 23, 556–561, 1989.
Ip, H. S. S., Huang, X. H. H., and Yu, J. Z.: Effective Henry's law constants of glyoxal, glyoxylic acid and glycolic acid, Geophys. Res. Lett., 36, L01802, https://doi.org/10.1029/2008GL036212, 2009.
Iraci, L. T., Baker, B. M., Tyndall, G. S., and Orlando, J. J.: Measurements of the Henry's Law Coefficients of 2-Methyl-3-buten-2-ol, Methacrolein, and Methylvinyl Ketone, J. Atmos. Chem., 33, 321–330, 1999.
Jacobson, M.: Isolating nitrated and aromatic aerosols and nitrated aromatic gases as sources of ultraviolet light absorption, J. Geophys. Res., 104, 3527–3542, 1999.
Jaoui, M., Edney, E. O., Kleindienst, T. E., Lewandowski, M., Offenberg, J. H., Surratt, J. D., and Seinfeld, J. H.: Formation of secondary organic aerosol from irradiated α-pinene/toluene/NOx mixtures and the effect of isoprene and sulfur dioxide, J. Geophys. Res., 113, D09303, https://doi.org/10.1029/2007jd009426, 2008.
Jathar, S. H., Farina, S. C., Robinson, A. L., and Adams, P. J.: The influence of semi-volatile and reactive primary emissions on the abundance and properties of global organic aerosol, Atmos. Chem. Phys., 11, 7727–7746, https://doi.org/10.5194/acp-11-7727-2011, 2011.
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, 5959, 1525–1529, https://doi.org/10.1126/science.1180353, 2009.
John, W., Wall, S. M., Ondo, J. L., and Winklmayr, W.: Modes in the size distributions of atmospheric inorganic aerosol, Atmos. Environ. A, 24, 2349–2359, https://doi.org/10.1016/0960-1686(90)90327-j, 1990.
Jung, J. and Kawamura, K.: Enhanced concentrations of citric acid in spring aerosols collected at the Gosan background site in East Asia, Atmos. Environ., 45, 5266-5272, https://doi.org/10.1016/j.atmosenv.2011.06.065, 2011.
Kanakidou, M., Seinfeld, J. H., Pandis, S. N., Barnes, I., Dentener, F. J., Facchini, M. C., Van Dingenen, R., Ervens, B., Nenes, A., Nielsen, C. J., Swietlicki, E., Putaud, J. P., Balkanski, Y., Fuzzi, S., Horth, J., Moortgat, G. K., Winterhalter, R., Myhre, C. E. L., Tsigaridis, K., Vignati, E., Stephanou, E. G., and Wilson, J.: Organic aerosol and global climate modelling: a review, Atmos. Chem. Phys., 5, 1053–1123, https://doi.org/10.5194/acp-5-1053-2005, 2005.
Karpel Vel Leitner, N., and Doré, M.: Mecanisme d'action des radicaux OH sur les acides glycolique, glyoxylique, acetique et oxalique en solution aqueuse: Incidence sur la consammation de peroxyde d'hydrogene dans les systemes H2O2/UV et O3/H2O2 (Mechanism of the reaction between hydroxyl radicals and glycolic, glyoxylic, acetic and oxalic acids in aqueous solution: Consequence on hydrogen peroxide consumption in the H2O2/UV and O3/H2O2 systems), Water Research, 31, 1383–1397, 1997.
Kaul, D. S., Gupta, T., Tripathi, S. N., Tare, V., and Collett, J. L.: Secondary Organic Aerosol: A Comparison between Foggy and Nonfoggy Days, Environ. Sci. Technol., 45, 7307–7313, https://doi.org/10.1021/es201081d, 2011.
Kawamura, K. and Kaplan, I. R.: Motor Exhaust Emissions as Primary Source for Dicarboxylic Acids in Los Angeles Ambient Air, Environ. Sci. Technol, 21, 105–110, 1987.
Kawamura, K., Kasukabe, H., and Barrie, L. A.: Source and reaction pathways of dicarboxylic acids, ketoacids and dicarbonyls in Arctic aerosols: One year of observations, Atmos. Environ., 30, 1709–1722, 1996a.
Kawamura, K., Steinberg, S., and Kaplan, I. R.: Concentrations of monocarboxylic and dicarboxylic acids and aldehydes in Southern California wet precipitations: comparison of urban and non-urban samples and compositional changes during scavenging, Atmos. Environ., 30, 1035–1052, 1996b.
Kawamura, K. and Sakaguchi, F.: Molecular distributions of water soluble dicarboxylic acids in marine aerosols over the Pacific Ocean including tropics, J. Geophys. Res., 104, 3501–3509, 1999.
Kawamura, K., Steinberg, S., and Kaplan, I. R.: Homologous series of C1-C10 monocarboxylic acids and C1-C6 carbonyls in Los Angeles air and motor vehicle exhausts, Atmos. Environ., 34, 4175–4191, 2000.
Kawamura, K., Umemoto, N., Mochida, M., Bertram, T., Howell, S., and Huebert, B. J.: Water-soluble dicarboxylic acids in the tropospheric aerosols collected over east Asia and western North Pacific by ACE-Asia C-130 aircraft, J. Geophys. Res., 108, 8639, https://doi.org/10.1029/2002JD003256, 2003.
Kawamura, K., Kasukabe, H., and Barrie, L. A.: Secondary formation of water-soluble organic acids and α-dicarbonyls and their contributions to total carbon and water-soluble organic carbon: Photochemical aging of organic aerosols in the Arctic spring, J. Geophys. Res., 115, D21306, https://doi.org/10.1029/2010jd014299, 2010.
Kerminen, V.-M. and Wexler, A. S.: Growth laws for atmospheric aerosol particles: An examination of the bimodality of the accumulation mode, Atmos. Environ., 29, 3263–3275, https://doi.org/10.1016/1352-2310(95)00249-x, 1995.
Kirchstetter, T., Novakov, T., and Hobbs, P. V.: Evidence that the spectral dependence of light absorption by aerosols is affected by organic carbon, J. Geophys. Res., 109, D21208, https://doi.org/10.1029/2004JD004999, 2004.
Kristensen, K. and Glasius, M.: Organosulfates and oxidation products from biogenic hydrocarbons in fine aerosols from a forest in North West Europe during spring, Atmos. Environ., 45, 4546–4556, https://doi.org/10.1016/j.atmosenv.2011.05.063, 2011.
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, 2008.
Krizner, H. E., DeHaan, D. O., and Kua, K.: Thermodynamics and kinetics of methylglyoxal dimer formation: A computational study, J. Phys Chem. A, 113, 25, 6994–7001, 2009.
Kroll, J. H., Ng, N. L., Murphy, S. M., Flagan, R. C., and Seinfeld, J. H.: Secondary organic aerosol formation from isoprene photooxidation under high NOx conditions, Geophys. Res. Lett., 32, L18808, https://doi.org/10.1029/2005GL023637, 2005a.
Kroll, J. H., Ng, N. L., Murphy, S. M., Varutbangkul, V., Flagan, R. C., and Seinfeld, J. H.: Chamber studies of secondary organic aerosol growth by reactive uptake of simple carbonyl compounds, J. Geophys. Res., 110, D23207, https://doi.org/10.1029/2005JD006004, 2005b.
Kroll, J. H., Donahue, N. M., Jimenez, J. L., Kessler, S. H., Canagaratna, M. R., Wilson, K. R., Altieri, K. E., Mazzoleni, L. R., Wozniak, A. S., Bluhm, H., Mysak, E. R., Smith, J. D., Kolb, C. E., and Worsnop, D. R.: Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol, Nat. Chem., 3, 133–139, 2011.
Kua, J., Hanley, S. W., and DeHaan, D. O.: Thermodynamics and kinetics of glyoxal dimer formation: A computational study, J. Phys. Chem. A, 112, 66–72, 2008.
Kua, J., Krizner, H. E., and De Haan, D. O.: Thermodynamics and Kinetics of Imidazole Formation from Glyoxal, Methylamine, and Formaldehyde: A Computational Study, J. Phys. Chem. A, 115, 1667–1675, https://doi.org/10.1021/jp111527x, 2011.
Lambe, A. T., Onasch, T. B., Massoli, P., Croasdale, D. R., Wright, J. P., Ahern, A. T., Williams, L. R., Worsnop, D. R., Brune, W. H., and Davidovits, P.: Laboratory studies of the chemical composition and cloud condensation nuclei (CCN) activity of secondary organic aerosol (SOA) and oxidized primary organic aerosol (OPOA), Atmos. Chem. Phys., 11, 8913–8928, https://doi.org/10.5194/acp-11-8913-2011, 2011.
Lee-Taylor, J., Madronich, S., Aumont, B., Camredon, M., Hodzic, A., Tyndall, G. S., Apel, E., and Zaveri, R. A.: Explicit modeling of organic chemistry and secondary organic aerosol partitioning for Mexico City and its outflow plume, Atmos. Chem. Phys. Discuss., 11, 17013–17070, https://doi.org/10.5194/acpd-11-17013-2011, 2011.
Lee, A. K. Y., Herckes, P., Leaitch, W. R., Macdonald, A. M., and Abbatt, J. P. D.: Aqueous OH oxidation of ambient organic aerosol and cloud water organics: Formation of highly oxidized products, Geophys. Res. Lett., 38, 11, L11805, https://doi.org/10.1029/2011gl047439, 2011.
Lee, S., Murphy, D. M., Thomson, D. S., and Middlebrook, A. M.: Nitrate and oxidized organic ions in single particle mass spectra during the 1999 Atlanta Supersite Project, J. Geophys. Res., 108, 8417, https://doi.org/10.1029/2001JD001455, 2003.
Li, Z., Schwier, A. N., Sareen, N., and McNeill, V. F.: Reactive processing of formaldehyde and acetaldehyde in aqueous aerosol mimics: surface tension depression and secondary organic products, Atmos. Chem. Phys. Discuss., 11, 19477–19506, https://doi.org/10.5194/acpd-11-19477-2011, 2011.
Liggio, J., Li, S.-M., and McLaren, R.: Heterogeneous reactions of glyoxal on particulate matter: identification of acetals and sulfate esters, Environ. Sci. Technol., 39, 1532–1541, 2005a.
Liggio, J., Li, S.-M., and McLaren, R.: Reactive uptake of glyoxal by particulate matter, J. Geophys. Res., 110, D10304,https://doi.org/10.1029/2004JD005113, 2005b.
Likens, G. E., Edgerton, E. S., and Galloway, J. N.: The composition and deposition of organic carbon in precipitation, Tellus B, 35B, 16–24, https://doi.org/10.1111/j.1600-0889.1983.tb00003.x, 1983.
Lim, Y. B., Tan, Y., Perri, M. J., Seitzinger, S. P., and Turpin, B. J.: Aqueous chemistry and its role in secondary organic aerosol (SOA) formation, Atmos. Chem. Phys., 10, 10521–10539, https://doi.org/10.5194/acp-10-10521-2010, 2010.
Lin, P., Engling, G., and Yu, J. Z.: Humic-like substances in fresh emissions of rice straw burning and in ambient aerosols in the Pearl River Delta Region, China, Atmos. Chem. Phys., 10, 6487–6500, https://doi.org/10.5194/acp-10-6487-2010, 2010a.
Lin, P., Huang, X.-F., He, L.-Y., and Zhen Yu, J.: Abundance and size distribution of HULIS in ambient aerosols at a rural site in South China, J. Aerosol Sci., 41, 74–87, 2010b.
Liu, Y., El Haddad, I., Scarfogliero, M., Nieto-Gligorovski, L., Temime-Roussel, B., Quivet, E., Marchand, N., Picquet-Varrault, B., and Monod, A.: In-cloud processes of methacrolein under simulated conditions – Part 1: Aqueous phase photooxidation, Atmos. Chem. Phys., 9, 5093–5105, https://doi.org/10.5194/acp-9-5093-2009, 2009.
Liu, Y., Tritscher, T., Praplan, A. P., DeCarlo, P. F., Temime-Roussel, B., Quivet, E., Marchand, N., Dommen, J., Baltensperger, U., and Monod, A.: Aqueous phase processing of secondary organic aerosols, Atmos. Chem. Phys. Discuss., 11, 21489–21532, https://doi.org/10.5194/acpd-11-21489-2011, 2011.
Marcolli, C. and Peter, Th.: Water activity in polyol/water systems: new UNIFAC parameterization, Atmos. Chem. Phys., 5, 1545–1555, https://doi.org/10.5194/acp-5-1545-2005, 2005.
Maria, S. F., L. M. Russell, M. K. Gilles, and Myeni, S. C. B.: Organic Aerosol Growth Mechanisms and Their Climate Forcing Implications, Science, 306, 1921–1924, 2004.
Martin, S. T., Andreae, M. O., Althausen, D., Artaxo, P., Baars, H., Borrmann, S., Chen, Q., Farmer, D. K., Guenther, A., Gunthe, S. S., Jimenez, J. L., Karl, T., Longo, K., Manzi, A., Müller, T., Pauliquevis, T., Petters, M. D., Prenni, A. J., Pöschl, U., Rizzo, L. V., Schneider, J., Smith, J. N., Swietlicki, E., Tota, J., Wang, J., Wiedensohler, A., and Zorn, S. R.: An overview of the Amazonian Aerosol Characterization Experiment 2008 (AMAZE-08), Atmos. Chem. Phys., 10, 11415–11438, https://doi.org/10.5194/acp-10-11415-2010, 2010.
Martinelango, P. K., Dasgupta, P. K., and Al-Horr, R. S.: Atmospheric production of oxalic acid/oxalate and nitric acid/nitrate in the Tampa Bay airshed: Parallel pathways, Atmos. Environ., 41, 4258–4269, 2007.
Massoli, P., Lambe, A. T., Ahern, A. T., Williams, L. R., Ehn, M., Mikkilä, J., Canagaratna, M. R., Brune, W. H., Onasch, T. B., Jayne, J. T., Petäjä, T., Kulmala, M., Laaksonen, A., Kolb, C. E., Davidovits, P., and Worsnop, D. R.: Relationship between aerosol oxidation level and hygroscopic properties of laboratory generated secondary organic aerosol (SOA) particles, Geophys. Res. Lett., 37, L24801, https://doi.org/10.1029/2010gl045258, 2010.
Mazzoleni, L. R., Ehrmann, B. M., Shen, X., Marshall, A. G., and Collett, J. L.: Water-Soluble Atmospheric Organic Matter in Fog: Exact Masses and Chemical Formula Identification by Ultrahigh-Resolution Fourier Transform Ion Cyclotron Resonance Mass Spectrometry, Environ. Sci. Technol., 44, 3690–3697, https://doi.org/10.1021/es903409k, 2010.
Meng, Z. and Seinfeld, J. H.: On the Source of the Submicrometer Droplet Mode of Urban and Regional Aerosols, Aerosol Sci. Technol., 20, 253–265, 1994.
Meng, Z., Seinfeld, J. H., Saxena, P., and Kim, Y. P.: Contribution of Water to Particulate Mass in the South Coast Air Basin, Aerosol Sci. Technol., 22, 111–123, 1995.
Michaud, V., El Haddad, I., Yao Liu, Sellegri, K., Laj, P., Villani, P., Picard, D., Marchand, N., and Monod, A.: In-cloud processes of methacrolein under simulated conditions – Part 3: Hygroscopic and volatility properties of the formed secondary organic aerosol, Atmos. Chem. Phys., 9, 5119–5130, https://doi.org/10.5194/acp-9-5119-2009, 2009.
Minakata, D., Li, K., Westerhoff, P., and Crittenden, J.: Development of a Group Contribution Method To Predict Aqueous Phase Hydroxyl Radical (HO) Reaction Rate Constants, Environ. Sci Technol., 43, 6220–6227, https://doi.org/10.1021/es900956c, 2009.
Minerath, E. C. and Elrod, M. J.: Assessing the Potential for Diol and Hydroxy Sulfate Ester Formation from the Reaction of Epoxides in Tropospheric Aerosols, Environ. Sci Technol., 43, 1386–1392, https://doi.org/10.1021/es8029076, 2009.
Miyazaki, Y., Aggarwal, S. G., Singh, K., Gupta, P. K., and Kawamura, K.: Dicarboxylic acids and water-soluble organic carbon in aerosols in New Delhi, India, in winter: Characteristics and formation processes, J. Geophys. Res., 114, D19206, https://doi.org/10.1029/2009jd011790, 2009a.
Miyazaki, Y., Kondo, Y., Shiraiwa, M., Takegawa, N., Miyakawa, T., Han, S., Kita, K., Hu, M., Deng, Z. Q., Zhao, Y., Sugimoto, N., Blake, D. R., and Weber, R. J.: Chemical characterization of water-soluble organic carbon aerosols at a rural site in the Pearl River Delta, China, in the summer of 2006, J. Geophys. Res., 114, D14208, https://doi.org/10.1029/2009jd011736, 2009b.
Moffett, R. C., Qin, X., Rebotier, T., Furutani, H., and Prather, K. A.: Chemically segregated optical and microphysical properties of ambient aerosols measured in a single-particle mass spectrometer, J. Geophys. Res., 113, D12213, https://doi.org/10.1029/2007JD009393, 2008.
Molina, M. J., Ivanov, A. V., Trakhtenberg, S., and Molina, L. T.: Atmospheric evolution of organic aerosol, Geophys. Res. Lett., 31, L22104, https://doi.org/10.1029/2004GL020910, 2004.
Monod, A. and Doussin, J. F.: Structure-activity relationship for the estimation of OH-oxidation rate constants of aliphatic organic compounds in the aqueous phase: alkanes, alcohols, organic acids and bases, Atmos. Environ., 42, 7611–7622, https://doi.org/10.1016/j.atmosenv.2008.06.005, 2008.
Monod, A., Poulain, L., Grubert, S., Voisin, D., and Wortham, H.: Kinetics of OH-initiated oxidation of oxygenated organic compounds in the aqueous phase: new rate constants, structure-activity relationships and atmospheric implications, Atmos. Environ., 39, 7667–7688, 2005.
Munger, J. W., Tiller, C., and Hoffmann, M. R.: Identification of Hydroxymethanesulfonate in Fog Water, Science, 231, 247–249, 1986.
Munger, J. W., Jacob, D. J., Daube , B. C., Horowitz, L. W., Keene, W. C., and Heikes, B. C.: Formaldehyde, glyoxal and methylglyoxal at a rural mountain site in central Virginia, J. Geophys. Res., 100, 9325–9333, 1995.
Murphy, B. N. and Pandis, S. N.: Simulating the Formation of Semivolatile Primary and Secondary Organic Aerosol in a Regional Chemical Transport Model, Environ. Sci Technol., 43, 4722–4728, https://doi.org/10.1021/es803168a, 2009.
Myriokefalitakis, S., Vrekoussis, M., Tsigaridis, K., Wittrock, F., Richter, A., Brühl, C., Volkamer, R., Burrows, J. P., and Kanakidou, M.: The influence of natural and anthropogenic secondary sources on the glyoxal global distribution, Atmos. Chem. Phys., 8, 4965–4981, http://dx.doi.org/10.5194/acp-8-4965-2008https://doi.org/10.5194/acp-8-4965-2008, 2008.
Myriokefalitakis, S., Tsigaridis, K., Mihalopoulos, N., Sciare, J., Nenes, A., Kawamura, K., Segers, A., and Kanakidou, M.: In-cloud oxalate formation in the global troposphere: a 3-D modeling study, Atmos. Chem. Phys., 11, 5761–5782, https://doi.org/10.5194/acp-11-5761-2011, 2011.
Nakayama, T., Matsumi, Y., Sato, K., Imamura, T., Yamazaki, A., and Uchiyama, A.: Laboratory studies on optical properties of secondary organic aerosols generated during the photooxidation of toluene and the ozonolysis of $\alpha $-pinene, J. Geophys. Res., 115, D24204, https://doi.org/10.1029/2010jd014387, 2010.
Narukawa, M., Kawamura, K., Anlauf, K. G., and Barrie, L. A.: Fine and coarse modes of dicarboxylic acids in the Arctic aerosols collected during the Polar Sunrise Experiment 1997, J. Geophys. Res., 108, 4575, https://doi.org/10.1029/2003JD003646, 2003.
Neusüss, C., Pelzing, M., Plewka, A., and Herrmann, H.: A new analytical approach for size-resolved speciation of organic compounds in atmospheric aerosol particles: Methods and first results, J. Geophys. Res., 105, 4513–4527, https://doi.org/10.1029/1999jd901038, 2000.
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.
Ng, N. L., Canagaratna, M. R., Zhang, Q., Jimenez, J. L., Tian, J., Ulbrich, I. M., Kroll, J. H., Docherty, K. S., Chhabra, P. S., Bahreini, R., Murphy, S. M., Seinfeld, J. H., Hildebrandt, L., Donahue, N. M., DeCarlo, P. F., Lanz, V. A., Prévôt, A. S. H., Dinar, E., Rudich, Y., and Worsnop, D. R.: Organic aerosol components observed in Northern Hemispheric datasets from Aerosol Mass Spectrometry, Atmos. Chem. Phys., 10, 4625–4641, https://doi.org/10.5194/acp-10-4625-2010, 2010.
Nguyen, T. B., Roach, P. J., Laskin, J., Laskin, A., and Nizkorodov, S. A.: Effect of humidity on the composition of isoprene photooxidation secondary organic aerosol, Atmos. Chem. Phys., 11, 6931–6944, https://doi.org/10.5194/acp-11-6931-2011, 2011.
Nishino, N., Arey, J., and Atkinson, R.: Formation Yields of Glyoxal and Methylglyoxal from the Gas-Phase OH Radical-Initiated Reactions of Toluene, Xylenes, and Trimethylbenzenes as a Function of NO2 Concentration, J. Phys Chem. A, 114, 10140–10147, https://doi.org/10.1021/jp105112h, 2010.
Noziere, B., Voisin, D., Longfellow, C. A., Friedli, H., Henry, B. E., and Hanson, D. R.: The uptake of methyl vinyl ketone, methacrolein, and 2-methyl-3-butene-2-ol onto sulfuric acid solutions, J. Phys. Chem. A, 110 2387–2395, 2006.
Noziere, B., Dziedzic, P., and Cordova, A.: Products and kinetics of the liquid-phase reaction of glyoxal catalysed by ammonium ions (NH$_{4}^{+})$, J. Phys. Chem. A, 113, 231–237, 2009.
Noziere, B., Dziedzic, P., and Cordova, A.: Inorganic ammonium salts and carbonate salts are efficient catalysts for aldol condensation in atmospheric aerosols, Phys. Chem. Chem. Phys., 12, 3864–3872, 2010a.
Noziere, B., Ekström, S., Alsberg, T., and Holmström, S.: Radical-initiated formation of organosulfates and surfactants in atmospheric aerosols, Geophys. Res. Lett., 37, L05806, https://doi.org/10.1029/2009gl041683, 2010b.
Odum, J. R., Hoffmann, T., Bowman, F., Collins, D., Flagan, R. C., and Seinfeld, J. H.: Gas/particle partitioning and secondary organic aerosol yields, Environ. Sci. Technol., 30, 2580–2585, 1996.
Olson, C. N., Galloway, M. M., Yu, G., Hedman, C. J., Lockett, M. R., Yoon, T. P., Stone, E. A., Smith, L. M., and Keutsch, F. N.: Hydroxycarboxylic Acid-Derived Organosulfates: Synthesis, Stability and Quantification in Ambient Aerosol, Environ. Sci. Tech., 45, 6468–6474, 2011.
Olson, T. M. and Hoffmann, M. R.: Hydroxyalkylsulfonate formation: its role as a S(IV) reservoir in atmospheric water droplets, Atmos. Environ., 23, 985–997, 1989.
Orsini, D. A., Ma, Y., Sullivan, A., Sierau, B., Baumann, K., and Weber, R. J.: Refinements to the particle-into-liquid sampler (PILS) for ground and airborne measurements of water soluble aerosol composition, Atmos. Environ., 37, 1243–1259, https://doi.org/10.1016/s1352-2310(02)01015-4, 2003.
Padro, L. T., Tkacik, D., Lathem, T., Hennigan, C. J., Sullivan, A. P., Weber, R. J., Huey, L. G., and Nenes, A.: Investigation of CCN relevant properties and droplet growth kinetics of water-soluble aerosol fraction in Mecixo City, J. Geophys. Res., 115, D09204, https://doi.org/09210.01029/02009JD013195, 2010.
Pandis, S. N., Wexler, A. S., and Seinfeld, J. H.: Secondary organic aerosol formation and transport – II. Predicting the ambient secondary organic aerosol size distribution, Atmos. Environ. A, 27, 2403–2416, 1993.
Pang, Y., Turpin, B. J., and Gundel, L. A.: On the Importance of Organic Oxygen for Understanding Organic Aerosol Particles, Aeros. Sci. Technol., 40, 128–133, 2006.
Pankow, J. F.: An Absorption model of the gas/aerosol partitioning involved in the formation of secondary organic aerosol, Atmos. Environ., 28, 189–193, 1994a.
Pankow, J. F.: An absorption model of the gas/aerosol partitioning of organic compounds in the atmosphere, Atmos. Environ., 28, 185–188, 1994b.
Parikh, H. M., Carlton, A. G., Vizuete, W., and Kamens, R. M.: Modeling secondary organic aerosol using a dynamic partitioning approach incorporating particle aqueous-phase chemistry, Atmos. Environ., 45, 1126–1137, https://doi.org/10.1016/j.atmosenv.2010.11.027, 2011.
Peltier, R. E., Hecobian, A. H., Weber, R. J., Stohl, A., Atlas, E. L., Riemer, D. D., Blake, D. R., Apel, E., Campos, T., and Karl, T.: Investigating the sources and atmospheric processing of fine particles from Asia and the Northwestern United States measured during INTEX B, Atmos. Chem. Phys., 8, 1835–1853, https://doi.org/10.5194/acp-8-1835-2008, 2008.
Perri, M. J., Seitzinger, S., and Turpin, B. J.: Secondary organic aerosol production from aqueous photooxidation of glycolaldehyde: Laboratory experiments, Atmos. Environ., 43, 1487–1497, 2009.
Perri, M. J., Lim, Y. B., Seitzinger, S. P., and Turpin, B. J.: Organosulfates from glycolaldehyde in aqueous aerosols and clouds: Laboratory studies, Atmos. Environ., 44, 2658–2664, 2010.
Petters, M. D. and Kreidenweis, S. M.: A single parameter representation of hygroscopic growth and cloud condensation nucleus activity, Atmos. Chem. Phys., 7, 1961–1971, https://doi.org/10.5194/acp-7-1961-2007, 2007.
Petters, M. D., Prenni, A. J., Kreidenweis, S. M., DeMott, P. J., Matsunaga, A., Lim, Y. B., and Ziemann, P. J.: Chemical aging and the hydrophobic-hydrophilic conversion of carbonaceous aerosol, Geophys. Res. Lett., 33, L24806, https://doi.org/10.1029/2006GL027249, 2006.
Pfrang, C., Shiraiwa, M., and Pöschl, U.: Chemical ageing and transformation of diffusivity in semi-solid multi-component organic aerosol particles, Atmos. Chem. Phys., 11, 7343–7354, https://doi.org/10.5194/acp-11-7343-2011, 2011.
Pickle, T., Allen, D. T., and Pratsinis, S. E.: The sources and size distributions of aliphatic and carbonyl carbon in Los Angeles aerosol, Atmos. Environ. A, 24, 2221–2228, https://doi.org/10.1016/0960-1686(90)90253-j, 1990.
Pöschl, U.: Gas-particle interactions of tropospheric aerosols: Kinetic and thermodynamic perspectives of multiphase chemical reactions, amorphous organic substances, and the activation of cloud condensation nuclei, Atmos. Res., 101, 562–573, https://doi.org/10.1016/j.atmosres.2010.12.018, 2011.
Reutter, P., Su, H., Trentmann, J., Simmel, M., Rose, D., Gunthe, S. S., Wernli, H., Andreae, M. O., and Pöschl, U.: Aerosol- and updraft-limited regimes of cloud droplet formation: influence of particle number, size and hygroscopicity on the activation of cloud condensation nuclei (CCN), Atmos. Chem. Phys., 9, 7067–7080, https://doi.org/10.5194/acp-9-7067-2009, 2009.
Riemer, N., West, M., Zaveri, R., and Easter, R.: Estimating black carbon aging time-scales with a particle resolved aerosol model, J. Aerosol Sci., 1, 143–158, 2010.
Rinaldi, M., Decesari, S., Carbone, C., Finessi, E., Fuzzi, S., Ceburnis, D., O'Dowd, C., Sciare, J., Burrows, J., Vrekoussis, M., Ervens, B., Tsigaridis, K., and Facchini, M. C.: Evidence of a natural marine source of oxalic acid and a possible link to glyoxal, J. Geophys. Res., https://doi.org/10.1029/2011JD015659, in press, 2011.
Rissman, T., Nenes, A., and Seinfeld, J. H.: Chemical Amplification (or Dampening) of the Twomey effect: Conditions derived from Droplet Activation Theory, J. Atmos. Sci., 61, 919–930, 2004.
Robinson, A. L., Donahue, N. M., Shrivastava, M. K., Weitkamp, E. A., Sage, A. M., Grieshop, A. P., Lane, T. E., Pierce, J. R., and Pandis, S. N.: Rethinking organic aerosols: Semivolatile emissions and photochemical aging, Science, 315, 1259–1262, 2007.
Romakkaniemi, S., Kokkola, H., Smith, J. N., Prisle, N. L., Schwier, A. N., McNeill, V. F., and Laaksonen, A.: Partitioning of semivolatile surface-active compounds between bulk, surface and gas phase, Geophys. Res. Lett., 38, L03807, https://doi.org/10.1029/2010gl046147, 2011.
Romero, F. and Oehme, M.: Organosulfates – A new Component of Humic-Like Substances in Atmospheric Aerosols?, J. Atmos. Chem., 52, 283–294, 2005.
Sagebiel, J. C. and Seiber, J. N.: Studies in the occurrence and distribution of wood smoke makrker compounds in foggy atmospheres, Environ. Toxicol. Chem., 12, 813–822, 1993.
Salma, I. and Láng, G. G.: How many carboxyl groups does an average molecule of humic-like substances contain?, Atmos. Chem. Phys., 8, 5997–6002, https://doi.org/10.5194/acp-8-5997-2008, 2008.
Salma, I., Ocskay, R., and Láng, G. G.: Properties of atmospheric humic-like substances – water system, Atmos. Chem. Phys., 8, 2243–2254, http://dx.doi.org/10.5194/acp-8-2243-2008https://doi.org/10.5194/acp-8-2243-2008, 2008.
Sareen, N., Schwier, A. N., Shapiro, E. L., Mitroo, D., and McNeill, V. F.: Secondary organic material formed by methylglyoxal in aqueous aerosol mimics, Atmos. Chem. Phys., 10, 997–1016, https://doi.org/10.5194/acp-10-997-2010, 2010.
Schmitt-Kopplin, P., Gelencsér, A., Dabek-Zlotorzynska, E., Kiss, G., Hertkorn, N., Harir, M., Hong, Y., and Gebefugi, I.: Analysis of the Unresolved Organic Fraction in Atmospheric Aerosols with Ultrahigh-Resolution Mass Spectrometry and Nuclear Magnetic Resonance Spectroscopy: Organosulfates As Photochemical Smog Constituents, Anal. Chem., 82, 8017–8026, http://dx.doi.org/10.1021/ac101444rhttps://doi.org/10.1021/ac101444r, 2010.
Schwier, A. N., Sareen, N., Mitroo, D., Shapiro, E. L., and McNeill, V. F.: Glyoxal-Methylglyoxal Cross-Reactions in Secondary Organic Aerosol Formation, Environ. Sci Technol., 44, 6174–6182, https://doi.org/10.1021/es101225q, 2010.
Sciare, J., d'Argouges, O., Sarda-Estève, R., Gaimoz, C., Dolgorouky, C., Bonnaire, N., Favez, O., Bonsang, B., and Gros, V.: Large contribution of water-insoluble secondary organic aerosols in the region of Paris (France) during wintertime, J. Geophys. Res., in press, 2011.
Seinfeld, J. H. and Pandis, S. N.: Atmospheric chemistry and physics, John Wiley & Sons, New York, 1326 pp., 1998.
Shapiro, E. L., Szprengiel, J., Sareen, N., Jen, C. N., Giordano, M. R., and McNeill, V. F.: Light-absorbing secondary organic material formed by glyoxal in aqueous aerosol mimics, Atmos. Chem. Phys., 9, 2289–2300, https://doi.org/10.5194/acp-9-2289-2009, 2009.
Shen, H. and Anastasio, C.: Formation of hydroxyl radical from San Joaquin Valley particles extracted in a cell-free surrogate lung fluid, Atmos. Chem. Phys., 11, 9671–9682, https://doi.org/10.5194/acp-11-9671-2011, 2011.
Shiraiwa, M., Pfrang, C., and Pöschl, U.: Kinetic multi-layer model of aerosol surface and bulk chemistry (KM-SUB): the influence of interfacial transport and bulk diffusion on the oxidation of oleic acid by ozone, Atmos. Chem. Phys., 10, 3673–3691, https://doi.org/10.5194/acp-10-3673-2010, 2010.
Shrivastava, M. K., Lipsky, E. M., Stanier, C. O., and Robinson, A. L.: Modeling Semivolatile Organic Aerosol Mass Emissions from Combustion Systems, Environ. Sci. Technol., 40, 2671–2677, https://doi.org/10.1021/es0522231, 2006.
Sievering, H., Boatman, J., Gorman, E., Kim, Y., Anderson, L., Ennis, G., Luria, M., and Pandis, S.: Removal of sulphur from the marine boundary layer by ozone oxidation in sea-salt aerosols, Nature, 360, 571–573, 1992.
Simon, H., Bhave, P. V., Swall, J. L., Frank, N. H., and Malm, W. C.: Determining the spatial and seasonal variability in OM/OC ratios across the US using multiple regression, Atmos. Chem. Phys., 11, 2933–2949, https://doi.org/10.5194/acp-11-2933-2011, 2011.
Slowik, J. G., Stroud, C., Bottenheim, J. W., Brickell, P. C., Chang, R. Y.-W., Liggio, J., Makar, P. A., Martin, R. V., Moran, M. D., Shantz, N. C., Sjostedt, S. J., van Donkelaar, A., Vlasenko, A., Wiebe, H. A., Xia, A. G., Zhang, J., Leaitch, W. R., and Abbatt, J. P. D.: Characterization of a large biogenic secondary organic aerosol event from eastern Canadian forests, Atmos. Chem. Phys., 10, 2825–2845, https://doi.org/10.5194/acp-10-2825-2010, 2010.
Smith, M. L., Kuwata, M., and Martin, S. T.: Secondary Organic Material Produced by the Dark Ozonolysis of α-Pinene Minimally Affects the Deliquescence and Efflorescence of Ammonium Sulfate, Aerosol Sci. Technol., 45, 244–261, 2011.
Sorooshian, A., Brechtel, F. J., Ervens, B., Feingold, G., Varutbangkul, V., Bahreini, R., Murphy, S., Holloway, J. S., Atlas, E. L., Anlauf, K., Buzorius, G., Jonsson, H., Flagan, R. C., and Seinfeld, J. H.: Oxalic acid in clear and cloudy atmospheres: Analysis of data from International Consortium for Atmospheric Research on Transport and Transformation 2004, J. Geophys. Res., 111, D23S45, https://doi.org/10.1029/2005JD006880, 2006.
Sorooshian, A., Lu, M.-L., Brechtel, F. J., Jonsson, H., Feingold, G., Flagan, R. C., and Seinfeld, J. H.: On the source of organic acid aerosol layers above clouds, Environ. Sci. Technol., 41, 4647–4654, 2007.
Sorooshian, A., Murphy, S. M., Hersey, S., Bahreini, R., Jonsson, H., Flagan, R. C., and Seinfeld, J. H.: Constraining the contribution of organic acids and AMS m/z 44 to the organic aerosol budget: On the importance of meteorology, aerosol hygroscopicity, and region, Geophys. Res. Lett., 37, L21807, https://doi.org/10.1029/2010gl044951, 2010.
Spaulding, R. S., Schade, G. W., Goldstein, A. H., and Charles, M. J.: Characterization of secondary atmospheric photooxidation products: Evidence of biogenic and anthropogenic sources, J. Geophys. Res., 108, 4247, https://doi.org/10.1029/2002JD002478, 2003.
Spracklen, D. V., Jimenez, J. L., Carslaw, K. S., Worsnop, D. R., Evans, M. J., Mann, G. W., Zhang, Q., Canagaratna, M. R., Allan, J., Coe, H., McFiggans, G., Rap, A., and Forster, P.: Aerosol mass spectrometer constraint on the global secondary organic aerosol budget, Atmos. Chem. Phys. Discuss., 11, 5699–5755, https://doi.org/10.5194/acpd-11-5699-2011, 2011.
Stavrakou, T., Müller, J.-F., De Smedt, I., Van Roozendael, M., Kanakidou, M., Vrekoussis, M., Wittrock, F., Richter, A., and Burrows, J. P.: The continental source of glyoxal estimated by the synergistic use of spaceborne measurements and inverse modelling, Atmos. Chem. Phys., 9, 8431–8446, https://doi.org/10.5194/acp-9-8431-2009, 2009.
Stefan, M. I. and Bolton, J. R.: Reinvestigation of the acetone degradation mechanism in dilute aqueous solution by the UV/H2O2 process, Environ. Sci. Technol., 33, 870–873, 1999.
Steinbacher, M., Dommen, J., Ordonez, C., Reimann, S., Grübler, F. C., Staehelin, J., and Prevot, A. S. H.: Volatile Organic Compounds in the Po Basin. Part A: Anthropogenic VOCs, J. Atmos. Chem., 51, 271–291, https://doi.org/10.1007/s10874-005-3576-1, 2005.
Stone, E. A., Hedman, C. J., Sheesley, R. J., Shafer, M. M., and Schauer, J. J.: Investigating the chemical nature of humic-like substances (HULIS) in North American atmospheric aerosols by liquid chromatography tandem mass spectrometry, Atmos. Environ., 43, 4205–4213, https://doi.org/10.1016/j.atmosenv.2009.05.030, 2009.
Sullivan, A. P. and Weber, R. J.: Chemical characterization of the ambient organic aerosol soluble in water: 1. Isolation of hydrophobic and hydrophilic fractions with a XAD-8 resin, J. Geophys. Res., 111, D05314, https://doi.org/10.1029/2005jd006485, 2006a.
Sullivan, A. P. and Weber, R. J.: Chemical characterization of the ambient organic aerosol soluble in water: 2. Isolation of acid, neutral, and basic fractions by modified size-exclusion chromatography, J. Geophys. Res., 111, D05315, https://doi.org/10.1029/2005jd006486, 2006b.
Sullivan, R. C. and Prather, K. A.: Investigations of the diurnal cycle and mixing state of oxalic acid in individual particles in Asian aerosol outflow, Environ. Sci Technol., 41, 8062–8069, 2007.
Sun, Y. L., Zhang, Q., Anastasio, C., and Sun, J.: Insights into secondary organic aerosol formed via aqueous-phase reactions of phenolic compounds based on high resolution mass spectrometry, Atmos. Chem. Phys., 10, 4809–4822, https://doi.org/10.5194/acp-10-4809-2010, 2010.
Surratt, J. D., Kroll, J. H., Kleindienst, T. E., Edney, E. O., Claeys, M., Sorooshian, A., Ng, N. L., Offenberg, J. H., Lewandowski, M., Jaoui, M., Flagan, R. C., and Seinfeld, J. H.: Evidence for organosulfates in secondary organic aerosol, Environ. Sci. Technol., 41, 517–527, 2007a.
Surratt, J. D., Lewandowski, M., Offenberg, J. H., Jaoui, M., Kleindienst, T. E., Edney, E. O., and Seinfeld, J. H.: Effect of acidity on secondary organic aerosol formation from isoprene, Environ. Sci Technol., 41, 5363–5369, 2007b.
Tan, Y., Perri, M. J., Seitzinger, S. P., and Turpin, B. J.: Effects of Precursor Concentration and Acidic Sulfate in Aqueous Glyoxal-OH Radical Oxidation and Implications for Secondary Organic Aerosol, Environ. Sci. Technol., 43, 8105–8112, https://doi.org/10.1021/es901742f, 2009.
Tan, Y., Carlton, A. G., Seitzinger, S. P., and Turpin, B. J.: SOA from methylglyoxal in clouds and wet aerosols: Measurement and prediction of key products, Atmos. Environ., 44, 5218–5226, 2010.
Tan, Y., Lim, Y. B., Altieri, K. E., Seitzinger, S. P., and Turpin, B. J.: Mechanisms leading to oligomers and SOA through aqueous photooxidation: insights from OH radical oxidation of acetic acid, Atmos. Chem. Phys. Discuss., 11, 18319–18347, https://doi.org/10.5194/acpd-11-18319-2011, 2011.
Tang, Y., Thron, R. P., Mauldin, R. L., and Wine, P. H.: Kinetics and spectroscopy of the SO4- radical in aqueous solution, J. Photochem. and Photobiol. A, 44, 243–258, 1988.
Tilgner, A. and Herrmann, H.: Radical-driven carbonyl-to-acid conversion and acid degradation in tropospheric aqueous systems studied by CAPRAM, Atmos. Environ., 44, 5415–5422, 2010.
Trainic, M., Abo Riziq, A., Lavi, A., Flores, J. M., and Rudich, Y.: The optical, physical and chemical properties of the products of glyoxal uptake on ammonium sulfate seed aerosols, Atmos. Chem. Phys., 11, 9697–9707, https://doi.org/10.5194/acp-11-9697-2011, 2011.
Tsimpidi, A. P., Karydis, V. A., Zavala, M., Lei, W., Molina, L., Ulbrich, I. M., Jimenez, J. L., and Pandis, S. N.: Evaluation of the volatility basis-set approach for the simulation of organic aerosol formation in the Mexico City metropolitan area, Atmos. Chem. Phys., 10, 525–546, https://doi.org/10.5194/acp-10-525-2010, 2010.
Turpin, B. J. and Lim, H.: Species contributions to PM2.5 mass concentrations: Revisiting common assumptions for estimating organic mass, Aerosol Sci. Technol., 35, 602–610, 2001.
Turpin, B. J., Saxena, P., and Andrews, E.: Measuring and simulating particulate organics in the atmosphere: problems and prospects, Atmos. Environ., 34, 2983–3013, https://doi.org/10.1016/s1352-2310(99)00501-4, 2000.
Ulbrich, I. M., Canagaratna, M. R., Zhang, Q., Worsnop, D. R., and Jimenez, J. L.: Interpretation of organic components from Positive Matrix Factorization of aerosol mass spectrometric data, Atmos. Chem. Phys., 9, 2891–2918, https://doi.org/10.5194/acp-9-2891-2009, 2009.
Virtanen, A., Joutsensaari, J., Koop, T., Kannosto, J., Yli-Pirila, P., Leskinen, J., Makela, J. M., Holopainen, J. K., Pöschl, U., Kulmala, M., Worsnop, D. R., and Laaksonen, A.: An amorphous solid state of biogenic secondary organic aerosol particles, Nature, 467, 824–827, 2010.
Volkamer, R., Jimenez, J. L., SanMartini, F., Dzepina, K., Zhang, Q., Salcedo, D., Molina, L. T., Worsnop, D. R., and Molina, M. J.: Secondary organic aerosol formation from anthropogenic air pollution: Rapid and higher than expected, Geophys. Res. Lett., 33, L17811, https://doi.org/10.1029/2006GL026899, 2006.
Volkamer, R., SanMartini, F., Molina, L. T., Salcedo, D., Jimenez, J., and Molina, M. J.: A missing sink for gas-phase glyoxal in Mexiko City: Formation of secondary organic aerosol, Geophys. Res. Lett., 34, L19807, https://doi.org/10.1029/2007GL030752, 2007.
Volkamer, R., Ziemann, P. J., and Molina, M. J.: Secondary Organic Aerosol Formation from Acetylene (C2H2): seed effect on SOA yields due to organic photochemistry in the aerosol aqueous phase, Atmos. Chem. Phys., 9, 1907–1928, https://doi.org/10.5194/acp-9-1907-2009, 2009.
von Hessberg, C., von Hessberg, P., Pöschl, U., Bilde, M., Nielsen, O. J., and Moortgat, G. K.: Temperature and humidity dependence of secondary organic aerosol yield from the ozonolysis of β-pinene, Atmos. Chem. Phys., 9, 3583–3599, https://doi.org/10.5194/acp-9-3583-2009, 2009.
Wang, J., Jacob, D. J., and Martin, S. T.: Sensitivity of sulfate direct climate forcing to the hysteresis of particle phase transitions, J. Geophys. Res., 113, D11207, https://doi.org/10.1029/2007jd009368, 2008.
Wang, J., Doussin, J.-F., Perrier, S., Perraudin, E., Katrib, Y., Pangui, E., and Picquet-Varrault, B.: Design of a new multi-phase experimental simulation chamber for atmospheric photosmog, aerosol and cloud chemistry research, Atmos. Meas. Tech. Discuss., 4, 315–384, https://doi.org/10.5194/amtd-4-315-2011, 2011.
Wang, L., Khalizov, A. F., Zheng, J., Xu, W., Ma, Y., Lal, V., and Zhang, R.: Atmospheric nanoparticles formed from heterogeneous reactions of organics, Nature Geosci., 3, 238–242, 2010.
Wang, L., Xu, W., Khalizov, A., Zheng, J., Qiu, C., and Zhang, R.: Laboratory Investigation on the Role of Organics in Atmospheric Nanoparticle Growth, J. Phys. Chem. A, 115, 8940–8947, https://doi.org/10.1021/jp1121855, 2011.
Wang, Y., Arellanes, C., Curtis, D. B., and Paulson, S. E.: Probing the Source of Hydrogen Peroxide Associated with Coarse Mode Aerosol Particles in Southern California, Environ. Sci. Technol., 44, 4070–4075, https://doi.org/10.1021/es100593k, 2010.
Warneck, P.: In-cloud chemistry opens pathway to the formation of oxalic acid in the marine atmosphere, Atmos. Environ., 37, 2423–2427, 2003.
Weber, R. J., Sullivan, A. P., Peltier, R. E., Russell, A., Yan, B., Zheng, M., DeGouw, J., Warneke, C., Brock, C., Holloway, J. S., Atlas, E. L., and Edgerton, E.: A study of secondary organic aerosol formation in the anthropogenic-influenced southeastern United States, J. Geophys. Res., 112, D13302, https://doi.org/10.1029/2007JD008408, 2007.
Whiteaker, J. and Prather, K. A.: Hydroxymethanesulfonate as a tracer for fog processing of individual aerosol particles, Atmos. Environ., 37, 1033–1043, 2003.
Yao, X., Fang, M., and Chan, C. K.: Size distributions and formation of dicarboxylic acids in atmospheric particles, Atmos. Environ., 36, 2099–2107, 2002.
Yao, X., Lau, A. P. S., Fang, M., Chan, C. K., and Hu, M.: Size distribution and formation of ionic species in atmospheric particulate pollutants in Beijing, China: 2. dicarboxylic acids, Atmos. Environ., 37, 3001–3007, 2003.
Yasmeen, F., Sauret, N., Gal, J.-F., Maria, P.-C., Massi, L., Maenhaut, W., and Claeys, M.: Characterization of oligomers from methylglyoxal under dark conditions: a pathway to produce secondary organic aerosol through cloud processing during nighttime, Atmos. Chem. Phys., 10, 3803–3812, https://doi.org/10.5194/acp-10-3803-2010, 2010.
Yu, G., Bayer, A. R., Galloway, M. M., Korshavn, K. J., Fry, C. G., and Keutsch, F. N.: Glyoxal in Aqueous Ammonium Sulfate Solutions: Products, Kinetics and Hydration Effects, Environ. Sci. Tech., 45, 6336–6342, https://doi.org/10.1021/es200989n, 2011.
Yu, J. Z., Huang, X.-F., Xu, J., and Hu, M.: When Aerosol sulfate goes up, so does Oxalate: Implication for the Formation Mechanisms of Oxalate, Environ. Sci. Technol., 39, 128–133, 2005.
Zellner, R., Exner, M., and Herrmann, H.: Absolute OH Quantum Yields in the Laser Photolysis of Nitrate, Nitrite and Dissolved H2O2 at 308 and 351 nm in the Temperature Range of 278-353 K, J. Atmos. Chem., 10, 411–425, 1990.
Zhang, H. and Ying, Q.: Secondary organic aerosol formation and source apportionment in Southeast Texas, Atmos. Environ., 45, 3217–3227, https://doi.org/10.1016/j.atmosenv.2011.03.046, 2011.
Zhang, H., Surratt, J. D., Lin, Y. H., Bapat, J., and Kamens, R. M.: Effect of relative humidity on SOA formation from isoprene/NO photooxidation: enhancement of 2-methylglyceric acid and its corresponding oligoesters under dry conditions, Atmos. Chem. Phys., 11, 6411–6424, https://doi.org/10.5194/acp-11-6411-2011, 2011.
Zhang, X., Chen, Z. M., and Zhao, Y.: Laboratory simulation for the aqueous OH-oxidation of methyl vinyl ketone and methacrolein: significance to the in-cloud SOA production, Atmos. Chem. Phys., 10, 9551–9561, https://doi.org/10.5194/acp-10-9551-2010, 2010.
Zhang, X., Liu, J., Lin, Y., Surratt, J. D., Hayes, P. L., Jimenez, J. L., Parker, E. T., and Weber, R. J.: Evidence for different formation pathways of soluble organic aerosols in two urban atmospheres with contrasting emissions, in preparation, 2011.
Ziemann, P. J.: Atmospheric Chemistry: Phase matters for aerosols, Nature, 467, 797–798, 2010.
Zuend, A., Marcolli, C., Luo, B. P., and Peter, T.: A thermodynamic model of mixed organic-inorganic aerosols to predict activity coefficients, Atmos. Chem. Phys., 8, 4559–4593, https://doi.org/10.5194/acp-8-4559-2008, 2008.
Zuend, A., Marcolli, C., Booth, A. M., Lienhard, D. M., Soonsin, V., Krieger, U. K., Topping, D. O., McFiggans, G., Peter, T., and Seinfeld, J. H.: New and extended parameterization of the thermodynamic model AIOMFAC: calculation of activity coefficients for organic-inorganic mixtures containing carboxyl, hydroxyl, carbonyl, ether, ester, alkenyl, alkyl, and aromatic functional groups, Atmos. Chem. Phys., 11, 9155–9206, https://doi.org/10.5194/acp-11-9155-2011, 2011.
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