Articles | Volume 19, issue 13
https://doi.org/10.5194/acp-19-8915-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-19-8915-2019
© Author(s) 2019. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
12 Jul 2019
Research article |
| 12 Jul 2019
| 12 Jul 2019
Temperature effects on sulfuric acid aerosol nucleation and growth: initial results from the TANGENT study
Lee Tiszenkel
Department of Atmospheric Science, University of Alabama in
Huntsville, Huntsville, AL, USA
Chris Stangl
Department of Chemistry and Biochemistry, University of Delaware,
Newark, DE, USA
Justin Krasnomowitz
Department of Chemistry and Biochemistry, University of Delaware,
Newark, DE, USA
Qi Ouyang
Department of Atmospheric Science, University of Alabama in
Huntsville, Huntsville, AL, USA
Huan Yu
School of Environmental Science and Engineering, Nanjing University of Information Science and Technology, Nanjing, China
Michael J. Apsokardu
Department of Chemistry and Biochemistry, University of Delaware,
Newark, DE, USA
Murray V. Johnston
Department of Chemistry and Biochemistry, University of Delaware,
Newark, DE, USA
Department of Atmospheric Science, University of Alabama in
Huntsville, Huntsville, AL, USA
Department of Environmental Science and Engineering, Fudan University, Shanghai, China
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Lee Tiszenkel, James H. Flynn, and Shan-Hu Lee
Atmos. Chem. Phys., 24, 11351–11363, https://doi.org/10.5194/acp-24-11351-2024, https://doi.org/10.5194/acp-24-11351-2024, 2024
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Ammonia and amines are important ingredients for aerosol formation in urban environments, but the measurements of these compounds are extremely challenging. Our observations show that urban ammonia and amines in Houston are emitted from urban sources, and diurnal variations in their concentrations are likely governed by gas-to-particle conversion and emissions.
Vignesh Vasudevan-Geetha, Lee Tiszenkel, Zhizhao Wang, Robin Russo, Daniel Bryant, Julia Lee-Taylor, Kelley Barsanti, and Shan-Hu Lee
EGUsphere, https://doi.org/10.5194/egusphere-2024-2454, https://doi.org/10.5194/egusphere-2024-2454, 2024
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Our laboratory experiments using two high-resolution mass spectrometers show that these OOMs can also form within the particle phase, in addition to gas-to-particle conversion processes. Our results demonstrate that particle-phase formation processes can contribute to the formation and growth of new particles in biogenic environments.
Zachary Watson, Can Li, Fei Liu, Sean W. Freeman, Huanxin Zhang, Jun Wang, and Shan-Hu Lee
EGUsphere, https://doi.org/10.5194/egusphere-2025-1735, https://doi.org/10.5194/egusphere-2025-1735, 2025
This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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Air pollutants like sulfur dioxide cause direct impacts on human health and the environment. Our work estimated surface concentrations from satellite data using atmospheric models and machine learning compared to an air quality monitoring network. We found that both methods can accurately determine the locations and changes in sulfur dioxide, but the machine learning method had better accuracy. Both methods are useful for monitoring air quality in locations without ground-based measurements.
Lee Tiszenkel, James H. Flynn, and Shan-Hu Lee
Atmos. Chem. Phys., 24, 11351–11363, https://doi.org/10.5194/acp-24-11351-2024, https://doi.org/10.5194/acp-24-11351-2024, 2024
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Ammonia and amines are important ingredients for aerosol formation in urban environments, but the measurements of these compounds are extremely challenging. Our observations show that urban ammonia and amines in Houston are emitted from urban sources, and diurnal variations in their concentrations are likely governed by gas-to-particle conversion and emissions.
Vignesh Vasudevan-Geetha, Lee Tiszenkel, Zhizhao Wang, Robin Russo, Daniel Bryant, Julia Lee-Taylor, Kelley Barsanti, and Shan-Hu Lee
EGUsphere, https://doi.org/10.5194/egusphere-2024-2454, https://doi.org/10.5194/egusphere-2024-2454, 2024
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Our laboratory experiments using two high-resolution mass spectrometers show that these OOMs can also form within the particle phase, in addition to gas-to-particle conversion processes. Our results demonstrate that particle-phase formation processes can contribute to the formation and growth of new particles in biogenic environments.
Michael S. Taylor Jr., Devon N. Higgins, and Murray V. Johnston
Atmos. Meas. Tech., 15, 4663–4674, https://doi.org/10.5194/amt-15-4663-2022, https://doi.org/10.5194/amt-15-4663-2022, 2022
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This modelling study investigates the complex growth kinetics of ultrafine particles in a flow tube reactor. When both surface- and volume-limited growth processes occur, the particle diameter growth rate changes as a function of time in the flow tube. We show that this growth can be represented by a parameter (growth factor, GF) which can be obtained experimentally from the outlet-minus-inlet particle diameter change without foreknowledge of the chemical growth processes involved.
Jian Xu, Jia Chen, Na Zhao, Guochen Wang, Guangyuan Yu, Hao Li, Juntao Huo, Yanfen Lin, Qingyan Fu, Hongyu Guo, Congrui Deng, Shan-Hu Lee, Jianmin Chen, and Kan Huang
Atmos. Chem. Phys., 20, 7259–7269, https://doi.org/10.5194/acp-20-7259-2020, https://doi.org/10.5194/acp-20-7259-2020, 2020
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This study provided evidence that gas-particle partitioning of ammonia, as opposed to ammonia concentration, plays a critical role in the haze formation. A reduction in ammonia emissions alone may not reduce air pollution effectively, at least at rural agricultural sites in China.
Michael J. Apsokardu and Murray V. Johnston
Atmos. Chem. Phys., 18, 1895–1907, https://doi.org/10.5194/acp-18-1895-2018, https://doi.org/10.5194/acp-18-1895-2018, 2018
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The ability of particle-phase chemistry to alter the molecular composition and enhance the growth rate of nanoparticles is investigated through the use of a kinetic growth model. The effects of particle-phase chemistry are found to be most pronounced for particles larger than about 20 nm in diameter. The results are discussed in the context of recent experimental measurements of particle-size-dependent molecular composition.
Peijun Tu and Murray V. Johnston
Atmos. Chem. Phys., 17, 7593–7603, https://doi.org/10.5194/acp-17-7593-2017, https://doi.org/10.5194/acp-17-7593-2017, 2017
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In this study, we determined the particle-size-dependent molecular composition of secondary organic aerosol (SOA) that was produced from β-pinene, an important biogenic precursor. We find that the composition changes significantly with particle size, and these changes can be linked to changes in the chemical processes that contribute to particle growth. Measurements of this type can aid the modeling and prediction of SOA formation.
Jenni Kontkanen, Katrianne Lehtipalo, Lauri Ahonen, Juha Kangasluoma, Hanna E. Manninen, Jani Hakala, Clémence Rose, Karine Sellegri, Shan Xiao, Lin Wang, Ximeng Qi, Wei Nie, Aijun Ding, Huan Yu, Shanhu Lee, Veli-Matti Kerminen, Tuukka Petäjä, and Markku Kulmala
Atmos. Chem. Phys., 17, 2163–2187, https://doi.org/10.5194/acp-17-2163-2017, https://doi.org/10.5194/acp-17-2163-2017, 2017
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The concentrations of ~1–3 nm particles were investigated at nine sites around the world. Sub-3 nm particle concentrations were highest at the sites with strong anthropogenic influence. Electrically neutral particles dominated sub-3 nm particle concentrations in polluted environments and in boreal forest during spring and summer. Sub-3 nm particle concentrations were observed to be determined by the availability of precursor vapors rather than the sink caused by preexisting aerosol particles.
F. Yu, G. Luo, S. C. Pryor, P. R. Pillai, S. H. Lee, J. Ortega, J. J. Schwab, A. G. Hallar, W. R. Leaitch, V. P. Aneja, J. N. Smith, J. T. Walker, O. Hogrefe, and K. L. Demerjian
Atmos. Chem. Phys., 15, 13993–14003, https://doi.org/10.5194/acp-15-13993-2015, https://doi.org/10.5194/acp-15-13993-2015, 2015
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The role of low-volatility organics in new particle formation (NPF) in the atmosphere is assessed. An empirical formulation in which formation rate is a function of the concentrations of sulfuric acid and low-volatility organics significantly overpredicts NPF in the summer.
Two different schemes predict quite different nucleation rates (including their spatial patterns), concentrations of cloud condensation nuclei, and aerosol first indirect radiative forcing in North America.
H. Guo, L. Xu, A. Bougiatioti, K. M. Cerully, S. L. Capps, J. R. Hite Jr., A. G. Carlton, S.-H. Lee, M. H. Bergin, N. L. Ng, A. Nenes, and R. J. Weber
Atmos. Chem. Phys., 15, 5211–5228, https://doi.org/10.5194/acp-15-5211-2015, https://doi.org/10.5194/acp-15-5211-2015, 2015
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Particle pH can affect many aerosol processes, including gas-particle partitioning, SOA formation, and mobilization of toxic redox metals. pH is challenging to directly measure and often improperly characterized by proxies like ion balances or molar ratios of measured aerosol ionic species. We present a detailed analysis predicting pH with a thermodynamic model, verify the prediction, and test pH sensitivity to model inputs based on data from the SOAS field campaign.
Y. You, V. P. Kanawade, J. A. de Gouw, A. B. Guenther, S. Madronich, M. R. Sierra-Hernández, M. Lawler, J. N. Smith, S. Takahama, G. Ruggeri, A. Koss, K. Olson, K. Baumann, R. J. Weber, A. Nenes, H. Guo, E. S. Edgerton, L. Porcelli, W. H. Brune, A. H. Goldstein, and S.-H. Lee
Atmos. Chem. Phys., 14, 12181–12194, https://doi.org/10.5194/acp-14-12181-2014, https://doi.org/10.5194/acp-14-12181-2014, 2014
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Amiens play important roles in atmospheric secondary aerosol formation and human health, but the fast response measurements of amines are lacking. Here we show measurements in a southeastern US forest and a moderately polluted midwestern site. Our results show that gas to particle conversion is an important process that controls ambient amine concentrations and that biomass burning is an important source of amines.
M. R. Pennington, B. R. Bzdek, J. W. DePalma, J. N. Smith, A.-M. Kortelainen, L. Hildebrandt Ruiz, T. Petäjä, M. Kulmala, D. R. Worsnop, and M. V. Johnston
Atmos. Chem. Phys., 13, 10215–10225, https://doi.org/10.5194/acp-13-10215-2013, https://doi.org/10.5194/acp-13-10215-2013, 2013
L.-H. Young, S.-H. Lee, V. P. Kanawade, T.-C. Hsiao, Y. L. Lee, B.-F. Hwang, Y.-J. Liou, H.-T. Hsu, and P.-J. Tsai
Atmos. Chem. Phys., 13, 547–564, https://doi.org/10.5194/acp-13-547-2013, https://doi.org/10.5194/acp-13-547-2013, 2013
Related subject area
Subject: Aerosols | Research Activity: Laboratory Studies | Altitude Range: Troposphere | Science Focus: Chemistry (chemical composition and reactions)
The importance of burning conditions on the composition of domestic biomass-burning organic aerosol and the impact of atmospheric ageing
Heterogeneous phototransformation of halogenated polycyclic aromatic hydrocarbons: influencing factors, mechanisms and products
Boosting aerosol surface effects: strongly enhanced cooperative surface propensity of atmospherically relevant organic molecular ions in aqueous solution
The lifetimes and potential change in planetary albedo owing to the oxidation of thin surfactant organic films extracted from atmospheric aerosol by hydroxyl (OH) radicals at the air–water interface of particles
Exometabolomic exploration of culturable airborne microorganisms from an urban atmosphere
Measurement Report: Changes in ammonia emissions since the 18th century in south-eastern Europe inferred from an Elbrus (Caucasus, Russia) ice-core record
Atmospheric oxidation of 1,3-butadiene: influence of seed aerosol acidity and relative humidity on SOA composition and the production of air toxic compounds
Enhanced sulfate formation in mixed biomass burning and sea-salt interactions mediated by photosensitization: effects of chloride, nitrogen-containing compounds, and atmospheric aging
Heterogeneous formation and light absorption of secondary organic aerosols from acetone photochemical reactions: remarkably enhancing effects of seeds and ammonia
Secondary Organic Aerosol Formation from Nitrate Radical Oxidation of Styrene: Aerosol Yields, Chemical Composition, and Hydrolysis of Organic Nitrates
Experimental observation of the impact of nanostructure on hygroscopicity and reactivity of fatty acid atmospheric aerosol proxies
Technical note: High-resolution analyses of concentrations and sizes of refractory black carbon particles deposited in northwestern Greenland over the past 350 years – Part 1: Continuous flow analysis of the SIGMA-D ice core using the wide-range Single-Particle Soot Photometer and a high-efficiency nebulizer
The role of surface-active macromolecules in the ice nucleating ability of lignin, Snomax, and agricultural soil extracts
HOMs and SOA formation from the oxidation of α- and β-phellandrenes by NO3 radicals
Particulate emissions from cooking: emission factors, emission dynamics, and mass spectrometric analysis for different cooking methods
Hydrogen Peroxide Photoformation in Particulate Matter and its Contribution to S(IV) Oxidation During Winter in Fairbanks, Alaska
Nocturnal atmospheric synergistic oxidation reduces the formation of low-volatility organic compounds from biogenic emissions
The interplay between aqueous replacement reaction and the phase state of internally mixed organic/ammonium aerosols
Measurement report: The Fifth International Workshop on Ice Nucleation phase 1 (FIN-01): intercomparison of single-particle mass spectrometers
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
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
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
Technical Note: A technique to convert NO2 to NO2− with S(IV) and its application to measuring nitrate photolysis
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)
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
Rhianna L. Evans, Daniel J. Bryant, Aristeidis Voliotis, Dawei Hu, Huihui Wu, Sara Aisyah Syafira, Osayomwanbor E. Oghama, Gordon McFiggans, Jacqueline F. Hamilton, and Andrew R. Rickard
Atmos. Chem. Phys., 25, 4367–4389, https://doi.org/10.5194/acp-25-4367-2025, https://doi.org/10.5194/acp-25-4367-2025, 2025
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The chemical composition of organic aerosol derived from wood-burning emissions under different burning conditions was characterised. Fresh emissions from flaming and smouldering were largely aromatic in nature, whereas upon aging the aromatic content decreased. This decrease was greater for smouldering due to the loss of toxic polyaromatic species, whereas under flaming conditions highly toxic polyaromatic species were produced. These differences present an important challenge for future policy.
Yueyao Yang, Yahui Liu, Guohua Zhu, Bingcheng Lin, Shanshan Zhang, Xin Li, Fangxi Xu, He Niu, Rong Jin, and Minghui Zheng
Atmos. Chem. Phys., 25, 3981–3994, https://doi.org/10.5194/acp-25-3981-2025, https://doi.org/10.5194/acp-25-3981-2025, 2025
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Halogenated polycyclic aromatic hydrocarbons (XPAHs) are emerging pollutants. Stability during atmospheric transformation processes is crucial for predicting their environmental fate and assessing the associated risks. Here, we conducted field studies and laboratory simulation experiments to reveal the mechanisms, influencing factors and products for XPAHs' heterogeneous phototransformation. Results revealed that the conversion of XPAHs led to a reduction in environmental risk.
Harmanjot Kaur, Stephan Thürmer, Shirin Gholami, Bruno Credidio, Florian Trinter, Debora Vasconcelos, Ricardo Marinho, Joel Pinheiro, Hendrik Bluhm, Arnaldo Naves de Brito, Gunnar Öhrwall, Bernd Winter, and Olle Björneholm
Atmos. Chem. Phys., 25, 3503–3518, https://doi.org/10.5194/acp-25-3503-2025, https://doi.org/10.5194/acp-25-3503-2025, 2025
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Understanding the surface composition of aerosols is crucial for advancing climate models. We investigated the interface of single-component and mixed aqueous solutions of atmospherically relevant carboxylic acid and alkyl-ammonium ions using liquid-jet photoelectron spectroscopy. An exponential increase in surface propensity as a function of chain length was found for the single species, and cooperative effects in the mixtures cause a further drastic increase in surface solute concentration.
Rosalie H. Shepherd, Martin D. King, Andrew D. Ward, Edward J. Stuckey, Rebecca J. L. Welbourn, Neil Brough, Adam Milsom, Christian Pfrang, and Thomas Arnold
Atmos. Chem. Phys., 25, 2569–2588, https://doi.org/10.5194/acp-25-2569-2025, https://doi.org/10.5194/acp-25-2569-2025, 2025
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Thin film formation at the air–water interface from material extracted from atmospheric aerosol was demonstrated, supporting the core–shell morphology. Film thicknesses were approximately 10 Å and 17 Å for urban and remote extracts, respectively. Exposure to gas-phase OH radicals showed fast reactions and short lifetimes of around 1 h. The effect on the Earth's radiative balance indicated that removing half of the film could significantly increase the top-of-atmosphere albedo for urban films.
Rui Jin, Wei Hu, Peimin Duan, Ming Sheng, Dandan Liu, Ziye Huang, Mutong Niu, Libin Wu, Junjun Deng, and Pingqing Fu
Atmos. Chem. Phys., 25, 1805–1829, https://doi.org/10.5194/acp-25-1805-2025, https://doi.org/10.5194/acp-25-1805-2025, 2025
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The metabolic capacity of atmospheric microorganisms after settling into habitats is poorly understood. We studied the molecular composition of exometabolites for cultured typical airborne microbes and traced their metabolic processes. Bacteria and fungi produce highly oxidized exometabolites and have significant variations in metabolism among different strains. These insights are pivotal for assessing the biogeochemical impacts of atmospheric microorganisms following their deposition.
Michel Legrand, Mstislav Vorobyev, Daria Bokuchava, Stanislav Kutuzov, Andreas Plach, Andreas Stohl, Alexandra Khairedinova, Vladimir Mikhalenko, Maria Vinogradova, Sabine Eckhardt, and Susanne Preunkert
Atmos. Chem. Phys., 25, 1385–1399, https://doi.org/10.5194/acp-25-1385-2025, https://doi.org/10.5194/acp-25-1385-2025, 2025
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Past atmospheric NH3 pollution in south-eastern Europe was reconstructed by analysing ammonium in an ice core drilled at the Mount Elbrus (Caucasus, Russia). The observed 3.5-fold increase in ice concentrations between 1750 and 1990 CE is in good agreement with estimated past dominant ammonia emissions from agriculture, mainly from south European Russia and Türkiye. In contrast to present-day conditions, the ammonium level observed in 1750 CE indicates significant natural emissions at that time.
Mohammed Jaoui, Klara Nestorowicz, Krzysztof J. Rudzinski, Michael Lewandowski, Tadeusz E. Kleindienst, Julio Torres, Ewa Bulska, Witold Danikiewicz, and Rafal Szmigielski
Atmos. Chem. Phys., 25, 1401–1432, https://doi.org/10.5194/acp-25-1401-2025, https://doi.org/10.5194/acp-25-1401-2025, 2025
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Recent research has established the contribution of 1,3-butadiene (13BD) to organic aerosol formation with negative implications for urban air quality. Health effect studies have focused on whole particulate matter, but compounds responsible for adverse health effects remain uncertain. This study provides the effect of relative humidity and seed aerosol acidity on the chemical composition of aerosol formed from 13BD photooxidation.
Rongzhi Tang, Jialiang Ma, Ruifeng Zhang, Weizhen Cui, Yuanyuan Qin, Yangxi Chu, Yiming Qin, Alexander L. Vogel, and Chak K. Chan
Atmos. Chem. Phys., 25, 425–439, https://doi.org/10.5194/acp-25-425-2025, https://doi.org/10.5194/acp-25-425-2025, 2025
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This study provides laboratory evidence that the photosensitizers in biomass burning extracts can enhance sulfate formation in NaCl particles, primarily by triggering the formation of secondary oxidants under light and air conditions, with a lower contribution of direct photosensitization via triplets.
Si Zhang, Yining Gao, Xinbei Xu, Luyao Chen, Can Wu, Zheng Li, Rongjie Li, Binyu Xiao, Xiaodi Liu, Rui Li, Fan Zhang, and Gehui Wang
Atmos. Chem. Phys., 24, 14177–14190, https://doi.org/10.5194/acp-24-14177-2024, https://doi.org/10.5194/acp-24-14177-2024, 2024
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Secondary organic aerosols (SOAs) from acetone photooxidation in the presence of various seeds were studied to illustrate SOA formation kinetics under ammonia-rich conditions. The oxidation mechanism of acetone was investigated using an observation-based model incorporating a Master Chemical Mechanism model. A higher SOA yield of acetone was observed compared to methylglyoxal due to an enhanced uptake of the small photooxidation products of acetone.
Yuchen Wang, Xiang Zhang, Yuanlong Huang, Yutong Liang, and Nga L. Ng
EGUsphere, https://doi.org/10.5194/egusphere-2024-3849, https://doi.org/10.5194/egusphere-2024-3849, 2024
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This work provides the first fundamental laboratory data to evaluate SOA production from styrene+NO3 chemistry. Additionally, the formation mechanisms of aromatic ONs are reported for the first time, highlighting that previously identified nitroaromatics in ambient field campaigns can be aromatic ONs. Finally, the hydrolysis lifetime observed for ONs generated from styrene+NO3 oxidation can serve as experimentally constrained parameter for modeling hydrolysis of aromatic ONs in general.
Adam Milsom, Adam M. Squires, Ben Laurence, Ben Wōden, Andrew J. Smith, Andrew D. Ward, and Christian Pfrang
Atmos. Chem. Phys., 24, 13571–13586, https://doi.org/10.5194/acp-24-13571-2024, https://doi.org/10.5194/acp-24-13571-2024, 2024
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We followed nano-structural changes in mixtures found in urban organic aerosol emissions (oleic acid, sodium oleate and fructose) during humidity change and ozone exposure. We demonstrate that self-assembly of fatty acid nanostructures can impact water uptake and chemical reactivity, affecting atmospheric lifetimes, urban air quality (preventing harmful emissions from degradation and enabling their long-range transport) and climate (affecting cloud formation), with implications for human health.
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
Atmos. Chem. Phys., 24, 12985–13000, https://doi.org/10.5194/acp-24-12985-2024, https://doi.org/10.5194/acp-24-12985-2024, 2024
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We developed a continuous flow analysis system to analyze an ice core from northwestern Greenland and coupled it with an improved refractory black carbon (rBC) measurement technique. This allowed accurate high-resolution analyses of size distributions and concentrations of rBC particles with diameters of 70 nm–4 μm for the past 350 years. Our results provide crucial insights into rBC's climatic effects. We also found previous ice core studies substantially underestimated rBC mass concentrations.
Kathleen A. Thompson, Paul Bieber, Anna J. Miller, Nicole Link, Benjamin J. Murray, and Nadine Borduas-Dedekind
EGUsphere, https://doi.org/10.5194/egusphere-2024-2827, https://doi.org/10.5194/egusphere-2024-2827, 2024
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Lignin and Snomax are surface-active macromolecules that show a relationship between increasing concentrations, decreasing surface tension, and increasing ice-nucleating ability. However, this relationship did not hold for agricultural soil extracts collected in the UK and Canada. Hydrophobic interfaces play an important role in the ice-nucleating activity of organic matter; as the complexity of the sample increases, the hydrophobic interfaces in the bulk compete with the air-water interface.
Sergio Harb, Manuela Cirtog, Stéphanie Alage, Christopher Cantrell, Mathieu Cazaunau, Vincent Michoud, Edouard Pangui, Antonin Bergé, Chiara Giorio, Francesco Battaglia, and Bénédicte Picquet-Varrault
EGUsphere, https://doi.org/10.5194/egusphere-2024-3419, https://doi.org/10.5194/egusphere-2024-3419, 2024
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We investigated the reactions of α- and β-phellandrenes (from vegetation emissions) with NO3 radicals, a major nighttime oxidant from human activities. Using lab-based simulations, we examined these reactions and measured particle formation and by-products. Our findings reveal that α- and β-phellandrenes are efficient particle sources and enhance our understanding of biogenic-anthropogenic interactions and their contributions to atmospheric changes affecting climate and health.
Julia Pikmann, Frank Drewnick, Friederike Fachinger, and Stephan Borrmann
Atmos. Chem. Phys., 24, 12295–12321, https://doi.org/10.5194/acp-24-12295-2024, https://doi.org/10.5194/acp-24-12295-2024, 2024
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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 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 barbecuing as an especially strong source.
Michael Oluwatoyin Sunday, Laura Marie Dahler Heinlein, Junwei He, Allison Moon, Sukriti Kapur, Ting Fang, Kasey C. Edwards, Fangzhou Guo, Jack Dibb, James H. Flynn III, Becky Alexander, Manabu Shiraiwa, and Cort Anastasio
EGUsphere, https://doi.org/10.5194/egusphere-2024-3272, https://doi.org/10.5194/egusphere-2024-3272, 2024
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Hydrogen peroxide (HOOH) is an important oxidant that forms atmospheric sulfate. We demonstrate that illumination of brown carbon can rapidly form HOOH within particles, even under the low sunlight conditions of Fairbanks, Alaska during winter. This in-particle formation of HOOH is fast enough that it forms sulfate at significant rates. In contrast, the formation of HOOH in the gas phase during the campaign is expected to be negligible because of high NOx levels.
Han Zang, Zekun Luo, Chenxi Li, Ziyue Li, Dandan Huang, and Yue Zhao
Atmos. Chem. Phys., 24, 11701–11716, https://doi.org/10.5194/acp-24-11701-2024, https://doi.org/10.5194/acp-24-11701-2024, 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 modeling, 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.
Hui Yang, Fengfeng Dong, Li Xia, Qishen Huang, Shufeng Pang, and Yunhong Zhang
Atmos. Chem. Phys., 24, 11619–11635, https://doi.org/10.5194/acp-24-11619-2024, https://doi.org/10.5194/acp-24-11619-2024, 2024
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Atmospheric secondary aerosols, composed of organic and inorganic components, undergo complex reactions that impact their phase state. Using molecular spectroscopy, we showed that ammonium-promoted aqueous replacement reaction, unique to these aerosols, is closely linked to phase behavior. The interplay between reactions and aerosol phase state can cause atypical phase transition and irreversible changes in aerosol composition during hygroscopic cycles, further impacting atmospheric processes.
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
Atmos. Chem. Phys., 24, 10869–10891, https://doi.org/10.5194/acp-24-10869-2024, https://doi.org/10.5194/acp-24-10869-2024, 2024
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Single-particle mass spectrometry (SPMS) is commonly used to measure the chemical composition and mixing state of aerosol particles. Intercomparison of SPMS instruments 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 differentiated secondary organic aerosol, soot, and soil dust but had difficulties differentiating among minerals and dusts.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Cited articles
Almeida, J., Schobesberger, S., Kurten, A., Ortega, I. K.,
Kupiainen-Maatta, O., Praplan, A. P., Adamov, A., Amorim, A., Bianchi, F.,
Breitenlechner, M., David, A., Dommen, J., Donahue, N. M., Downard, A.,
Dunne, E., Duplissy, J., Ehrhart, S., Flagan, R. C., Franchin, A., Guida,
R., Hakala, J., Hansel, A., Heinritzi, M., Henschel, H., Jokinen, T.,
Junninen, H., Kajos, M., Kangasluoma, J., Keskinen, H., Kupc, A., Kurten,
T., Kvashin, A. N., Laaksonen, A., Lehtipalo, K., Leiminger, M., Leppa, J.,
Loukonen, V., Makhmutov, V., Mathot, S., McGrath, M. J., Nieminen, T.,
Olenius, T., Onnela, A., Petaja, T., Riccobono, F., Riipinen, I., Rissanen,
M., Rondo, L., Ruuskanen, T., Santos, F. D., Sarnela, N., Schallhart, S.,
Schnitzhofer, R., Seinfeld, J. H., Simon, M., Sipila, M., Stozhkov, Y.,
Stratmann, F., Tome, A., Trostl, J., Tsagkogeorgas, G., Vaattovaara, P.,
Viisanen, Y., Virtanen, A., Vrtala, A., Wagner, P. E., Weingartner, E., Wex,
H., Williamson, C., Wimmer, D., Ye, P., Yli-Juuti, T., Carslaw, K. S.,
Kulmala, M., Curtius, J., Baltensperger, U., Worsnop, D. R., Vehkamaki, H.,
and Kirkby, J.: Molecular understanding of sulphuric acid-amine particle
nucleation in the atmosphere, Nature, 502, 359–363, https://doi.org/10.1038/nature12663,
2013.
Benson, D. R., Young, L. H., Kameel, R., and Lee, S. H.: Laboratory-measured
sulfuric acid and water homogeneous nucleation rates from the SO2+OH reaction, Geophys. Res. Lett., 35, L11801, https://doi.org/10.1029/2008GL033387,
2008.
Benson, D. R., Erupe, M. E., and Lee, S. H.: Laboratory-measured
Benson, D. R., Markovich, A., Al-Refai, M., and Lee, S.-H.: A Chemical Ionization Mass Spectrometer for ambient measurements of Ammonia, Atmos. Meas. Tech., 3, 1075–1087, https://doi.org/10.5194/amt-3-1075-2010, 2010.
Benson, D. R., Yu, J. H., Markovich, A., and Lee, S.-H.: Ternary homogeneous nucleation of H2SO4, NH3, and H2O under conditions relevant to the lower troposphere, Atmos. Chem. Phys., 11, 4755–4766, https://doi.org/10.5194/acp-11-4755-2011, 2011.
Berndt, T., Sipilä, M., Stratmann, F., Petäjä, T., Vanhanen, J., Mikkilä, J., Patokoski, J., Taipale, R., Mauldin III, R. L., and Kulmala, M.: Enhancement of atmospheric H2SO4∕H2O nucleation: organic oxidation products versus amines, Atmos. Chem. Phys., 14, 751–764, https://doi.org/10.5194/acp-14-751-2014, 2014.
Brus, D., Hyvärinen, A.-P., Viisanen, Y., Kulmala, M., and Lihavainen, H.: Homogeneous nucleation of sulfuric acid and water mixture: experimental setup and first results, Atmos. Chem. Phys., 10, 2631–2641, https://doi.org/10.5194/acp-10-2631-2010, 2010.
Chen, M., Titcombe, M., Jiang, J. K., Jen, C., Kuang, C. A., Fischer, M. L.,
Eisele, F. L., Siepmann, J. I., Hanson, D. R., Zhao, J., and McMurry, P. H.:
Acid-base chemical reaction model for nucleation rates in the polluted
atmospheric boundary layer, P. Natl. Acad. Sci. USA, 109,
18713–18718, https://doi.org/10.1073/pnas.1210285109, 2012.
Clarke, A. D.: Atmospheric nuclei in the Pacific mid-troposphere: their
nature, concentration, and evolution, J. Geophys. Res., 98, 20633–20647,
1993.
Dunne, E. M., Gordon, H., Kürten, A., Almeida, J., Duplissy, J.,
Williamson, C., Ortega, I. K., Pringle, K. J., Adamov, A., Baltensperger,
U., Barmet, P., Benduhn, F., Bianchi, F., Breitenlechner, M., Clarke, A.,
Curtius, J., Dommen, J., Donahue, N. M., Ehrhart, S., Flagan, R. C.,
Franchin, A., Guida, R., Hakala, J., Hansel, A., Heinritzi, M., Jokinen, T.,
Kangasluoma, J., Kirkby, J., Kulmala, M., Kupc, A., Lawler, M. J.,
Lehtipalo, K., Makhmutov, V., Mann, G., Mathot, S., Merikanto, J.,
Miettinen, P., Nenes, A., Onnela, A., Rap, A., Reddington, C. L. S.,
Riccobono, F., Richards, N. A. D., Rissanen, M. P., Rondo, L., Sarnela, N.,
Schobesberger, S., Sengupta, K., Simon, M., Sipilä, M., Smith, J. N.,
Stozkhov, Y., Tomé, A., Tröstl, J., Wagner, P. E., Wimmer, D.,
Winkler, P. M., Worsnop, D. R., and Carslaw, K. S.: Global atmospheric
particle formation from CERN CLOUD measurements, Science, 354, 1119–1123,
2016.
Duplissy, J., Merikanto, J., Franchin, A., Tsagkogeorgas, G., Kangasluoma,
J., Wimmer, D., Vuollekoski, H., Schobesberger, S., Lehtipalo, K., Flagan,
R. C., Brus, D., Donahue, N. M., Vehkamäki, H., Almeida, J., Amorim, A.,
Barmet, P., Bianchi, F., Breitenlechner, M., Dunne, E. M., Guida, R.,
Henschel, H., Junninen, H., Kirkby, J., Kürten, A., Kupc, A.,
Määttänen, A., Makhmutov, V., Mathot, S., Nieminen, T., Onnela,
A., Praplan, A. P., Riccobono, F., Rondo, L., Steiner, G., Tome, A.,
Walther, H., Baltensperger, U., Carslaw, K. S., Dommen, J., Hansel, A.,
Petäjä, T., Sipilä, M., Stratmann, F., Vrtala, A., Wagner, P.
E., Worsnop, D. R., Curtius, J., and Kulmala, M.: Effect of ions on sulfuric
acid-water binary particle formation: 2. Experimental data and comparison
with QC-normalized classical nucleation theory, J. Geophys. Res., 121,
1752–1775, https://doi.org/10.1002/2015JD023539, 2016.
Eisele, F. L. and Tanner, D. J.: Measurements of gas phase concentrations
of H2SO4 and methane sulfonic acid and estimates of
H2SO4 production and loss in the atmosphere, J. Geophys. Res., 98,
9001–9010, 1993.
Erupe, M. E., Benson, D. R., Li, J., Young, L. H., Verheggen, B., Al-Refai,
M., Tahboub, O., Cunningham, V., Frimpong, F., Viggiano, A. A., and Lee, S.
H.: Correlation of aerosol nucleation rate with sulfuric acid and ammonia in
Kent, Ohio: An atmospheric observation, J. Geophys. Res., 115, D23216,
https://doi.org/10.1029/2010JD013942, 2010.
Erupe, M. E., Viggiano, A. A., and Lee, S.-H.: The effect of trimethylamine on atmospheric nucleation involving H2SO4, Atmos. Chem. Phys., 11, 4767–4775, https://doi.org/10.5194/acp-11-4767-2011, 2011.
Frege, C., Ortega, I. K., Rissanen, M. P., Praplan, A. P., Steiner, G., Heinritzi, M., Ahonen, L., Amorim, A., Bernhammer, A.-K., Bianchi, F., Brilke, S., Breitenlechner, M., Dada, L., Dias, A., Duplissy, J., Ehrhart, S., El-Haddad, I., Fischer, L., Fuchs, C., Garmash, O., Gonin, M., Hansel, A., Hoyle, C. R., Jokinen, T., Junninen, H., Kirkby, J., Kürten, A., Lehtipalo, K., Leiminger, M., Mauldin, R. L., Molteni, U., Nichman, L., Petäjä, T., Sarnela, N., Schobesberger, S., Simon, M., Sipilä, M., Stolzenburg, D., Tomé, A., Vogel, A. L., Wagner, A. C., Wagner, R., Xiao, M., Yan, C., Ye, P., Curtius, J., Donahue, N. M., Flagan, R. C., Kulmala, M., Worsnop, D. R., Winkler, P. M., Dommen, J., and Baltensperger, U.: Influence of temperature on the molecular composition of ions and charged clusters during pure biogenic nucleation, Atmos. Chem. Phys., 18, 65–79, https://doi.org/10.5194/acp-18-65-2018, 2018.
Glasoe, W. A., Volz, K., Panta, B., Freshour, N., Bachman, R., Hanson, D.
R., McMurry, P. H., and Jen, C.: Sulfuric acid nucleation: an experimental
study of the effect of seven bases, J. Geophys. Res., 120, 1933–1950, https://doi.org/10.1002/2014JD022730, 2015.
Gordon, H., Kirkby, J., Baltensperger, U., Bianchi, F., Breitenlechner, M.,
Curtius, J., Dias, A., Dommen, J., Donahue, N. M., Dunne, E. M., Duplissy,
J., Ehrhart, S., Flagan, R. C., Frege, C., Fuchs, C., Hansel, A., Hoyle, C.
R., Kulmala, M., Kurten, A., Lehtipalo, K., Makhmutov, V., Molteni, U.,
Rissanen, M. P., Stozkhov, Y., Trostl, J., Tsagkogeorgas, G., Wagner, R.,
Williamson, C., Wimmer, D., Winkler, P. M., Yan, C., and Carslaw, K. S.:
Causes and importance of new particle formation in the present-day and
preindustrial atmospheres, J. Geophys. Res.-Atmos., 122, 8739–8760, https://doi.org/10.1002/2017jd026844, 2017.
Guo, S., Hua, M., Zamor, M. L., Peng, J., Shang, D., Zheng, J., Du, Z., Wu,
Z., Shao, M., Zeng, L., Molina, M. J., and Zhang, R.: Elucidating severe
urban haze formation in China, P. Natl. Acad. Sci. USA, 49, 17373–17378,
2014.
Hanson, D. R. and Eisele, F. L.: Diffusion of H2SO4 in humidified
nitrogen: hydrated H2SO4, J. Phys. Chem., 104, 1715–1719, 2000.
Hanson, D. R., Bier, I., Panta, B., Jen, C. N., and McMurry, P. H.:
Computational Fluid Dynamics Studies of a Flow Reactor: Free Energies of
Clusters of Sulfuric Acid with NH3 or Dimethyl Amine, J. Phys. Chem. A,
121, 3976–3990, https://doi.org/10.1021/acs.jpca.7b00252, 2017.
Hung, H.-M. and Hoffmann, M. R.: Oxidation of gas-phase SO2 on the
surfaces of acidic microdroplets: Implications for sulfate and sulfate
radical anion formation in the atmospheric liquid phase, Environ. Sci.
Technol., 49, 13768–13776, 2015.
Jen, C. N., McMurry, P. H., and Hanson, D. R.: Stabilization of sulfuric
acid dimers by ammonia, methylamine, dimethylamine, and trimethylamine, J.
Geophys. Res., 119, 7502–7514, https://doi.org/10.1002/2014jd021592, 2014.
Jen, C. N., Zhao, J., McMurry, P. H., and Hanson, D. R.: Chemical ionization of clusters formed from sulfuric acid and dimethylamine or diamines, Atmos. Chem. Phys., 16, 12513–12529, https://doi.org/10.5194/acp-16-12513-2016, 2016.
Kanawade, V. P., Jobson, B. T., Guenther, A. B., Erupe, M. E., Pressley, S. N., Tripathi, S. N., and Lee, S.-H.: Isoprene suppression of new particle formation in a mixed deciduous forest, Atmos. Chem. Phys., 11, 6013–6027, https://doi.org/10.5194/acp-11-6013-2011, 2011.
Kashchiev, D.: On the relation between nucleation work, nucleus size, and
nucleation rate, J. Phys. Chem., 76, 5098–5102, https://doi.org/10.1063/1.442808, 1982.
Khamaganov, V. G. and Hites, R. A.: Rate Constants for the Gas-Phase
Reactions of Ozone with Isoprene, α- and β-Pinene, and
Limonene as a Function of Temperature, J. Phys. Chem. A,
105, 815–822, https://doi.org/10.1021/jp002730z, 2001.
Kirkby, J., Curtius, J., Almeida, J., Dunne, E., Duplissy, J., Ehrhart, S.,
Franchin, A., Gagne, S., Ickes, L., Kurten, A., Kupc, A., Metzger, A.,
Riccobono, F., Rondo, L., Schobesberger, S., Tsagkogeorgas, G., Wimmer, D.,
Amorim, A., Bianchi, F., Breitenlechner, M., David, A., Dommen, J., Downard,
A., Ehn, M., Flagan, R. C., Haider, S., Hansel, A., Hauser, D., Jud, W.,
Junninen, H., Kreissl, F., Kvashin, A. N., Laaksonen, A., Lehtipalo, K.,
Lima, J., Lovejoy, E. R., Makhmutov, V., Mathot, S., Mikkila, J.,
Minginette, P., Mogo, S., Nieminen, T., Onnela, A., Pereira, P., Petaja, T.,
Schnitzhofer, R., Seinfeld, J. H., Sipila, M., Stozhkov, Y., Stratmann, F.,
Tome, A., Vanhanen, J., Viisanen, Y., Vrtala, A., Wagner, P. E., Walther,
H., Weingartner, E., Wex, H., Winkler, P. M., Carslaw, K. S., Worsnop, D.
R., Baltensperger, U., and Kulmala, M.: Role of sulphuric acid, ammonia and
galactic cosmic rays in atmospheric aerosol nucleation, Nature, 476,
429–433, 2011.
Kirkby, J., Duplissy, J., Sengupta, K., Frege, C., Gordon, H., Williamson,
C., Heinritzi, M., Simon, M., Yan, C., Almeida, J., Tröstl, J.,
Nieminen, T., Ortega, I. K., Wagner, R., Adamov, A., Amorim, A., Bernhammer,
A.-K., Bianchi, F., Breitenlechner, M., Brilke, S., Chen, X., Craven, J.,
Dias, A., Ehrhart, S., Flagan, R. C., Franchin, A., Fuchs, C., Guida, R.,
Hakala, J., Hoyle, C. R., Jokinen, T., Junninen, H., Kangasluoma, J., Kim,
J., Krapf, M., Kürten, A., Laaksonen, A., Lehtipalo, K., Makhmutov, V.,
Mathot, S., Molteni, U., Onnela, A., Peräkylä, O., Piel, F.,
Petäjä, T., Praplan, A. P., Pringle, K., Rap, A., Richards, N. A.
D., Riipinen, I., Rissanen, M. P., Rondo, L., Sarnela, N., Schobesberger,
S., Scott, C. E., Seinfeld, J. H., Sipilä, M., Steiner, G., Stozhkov,
Y., Stratmann, F., Tomé, A., Virtanen, A., Vogel, A. L., Wagner, A. C.,
Wagner, P. E., Weingartner, E., Wimmer, D., Winkler, P. M., Ye, P., Zhang,
X., Hansel, A., Dommen, J., Donahue, N. M., Worsnop, D. R., Baltensperger,
U., Kulmala, M., Carslaw, K. S., and Curtius, J.: Ion-induced nucleation of
pure biogenic particles, Nature, 533, 521–526, https://doi.org/10.1038/nature17953, 2016.
Krasnomowitz, J. M., Apsokardu, M. J., Stangl, C. M., Tiszenkel, L., Ouyang,
Q., Lee, S., and Johnston, M. V.: Growth of Aitken mode ammonium sulfate
particles by α-pinene ozonolysis, Aerosol Sci. Tech.,
53, 406–418, https://doi.org/10.1080/02786826.2019.1568381, 2019.
Kulmala, M., Kontkanen, J., Junninen, H., Lehtipalo, K., Manninen, H. E.,
Nieminen, T., Petäjä, T., Sipilä, M., Schobesberger, S.,
Rantala, P., Franchin, A., Jokinen, T., Järvinen, E.,
Äijälä, M., Kangasluoma, J., Hakala, J., Aalto, P. P., Paasonen,
P., Mikkilä, J., Vanhanen, J., Aalto, J., Hakola, H., Makkonen, U.,
Ruuskanen, T., Mauldin, R. L., Duplissy, J., Vehkamäki, H., Bäck,
J., Kortelainen, A., Riipinen, I., Kurtén, T., Johnston, M. V., Smith,
J. N., Ehn, M., Mentel, T. F., Lehtinen, K. E. J., Laaksonen, A., Kerminen,
V. M., and Worsnop, D. R.: Direct observations of atmospheric aerosol
nucleation, Science, 339, 943–946, https://doi.org/10.1126/science.1227385, 2013.
Kulmala, M., Kerminen, V.-M., Petaja, T., Ding, A., and Wang, L.:
Atmospheric gas-to-particle conversion: why NPF events are observed in
megacities?, Faraday Discuss., 200, 271–288, https://doi.org/10.1039/c6fd00257a, 2017.
Kürten, A., Rondo, L., Ehrhart, S., and Curtius, J.: Calibration of a
chemical ionization mass spectrometer for the measurement of gaseous
sulfuric acid, J. Phys. Chem. A, 116, 6375–6386, https://doi.org/10.1021/jp212123n, 2012.
Kürten, A., Jokinen, T., Simon, M., Sipilä, M., Sarnela, N.,
Junninen, H., Adamov, A., Almeida, J., Amorim, A., Bianchi, F.,
Breitenlechner, M., Dommen, J., Donahue, N. M., Duplissy, J., Ehrhart, S.,
Flagan, R. C., Franchin, A., Hakala, J., Hansel, A., Heinritzi, M.,
Hutterli, M., Kangasluoma, J., Kirkby, J., Laaksonen, A., Lehtipalo, K.,
Leiminger, M., Makhmutov, V., Mathot, S., Onnela, A., Petäjä, T.,
Praplan, A. P., Riccobono, F., Rissanen, M. P., Rondo, L., Schobesberger,
S., Seinfeld, J. H., Steiner, G., Tomé, A., Tröstl, J., Winkler, P.
M., Williamson, C., Wimmer, D., Ye, P., Baltensperger, U., Carslaw, K. S.,
Kulmala, M., Worsnop, D. R., and Curtius, J.: Neutral molecular cluster
formation of sulfuric acid–dimethylamine observed in real time under
atmospheric conditions, P. Natl. Acad. Sci. USA, 111, 15019–15024, https://doi.org/10.1073/pnas.1404853111, 2014.
Kürten, A., Bianchi, F., Almeida, J., Kupiainen-Määttä, O.,
Dunne, E. M., Duplissy, J., Williamson, C., Barmet, P., Breitenlechner, M.,
Dommen, J., Donahue, N. M., Flagan, R. C., Franchin, A., Gordon, H., Hakala,
J., Hansel, A., Heinritzi, M., Ickes, L., Jokinen, T., Kangasluoma, J., Kim,
J., Kirkby, J., Kupc, A., Lehtipalo, K., Leiminger, M., Makhmutov, V.,
Onnela, A., Ortega, I. K., Petäjä, T., Praplan, A. P., Riccobono,
F., Rissanen, M. P., Rondo, L., Schnitzhofer, R., Schobesberger, S., Smith,
J. N., Steiner, G., Stozhkov, Y., Tomé, A., Tröstl, J.,
Tsagkogeorgas, G., Wagner, P. E., Wimmer, D., Ye, P., Baltensperger, U.,
Carslaw, K., Kulmala, M., and Curtius, J.: Experimental particle formation
rates spanning tropospheric sulfuric acid and ammonia abundances, ion
production rates, and temperatures, J. Geophys. Res., 121, 12377–12400, https://doi.org/10.1002/2015JD023908, 2016.
Lawler, M. J., Winkler, P. M., Kim, J., Ahlm, L., Tröstl, J., Praplan, A. P., Schobesberger, S., Kürten, A., Kirkby, J., Bianchi, F., Duplissy, J., Hansel, A., Jokinen, T., Keskinen, H., Lehtipalo, K., Leiminger, M., Petäjä, T., Rissanen, M., Rondo, L., Simon, M., Sipilä, M., Williamson, C., Wimmer, D., Riipinen, I., Virtanen, A., and Smith, J. N.: Unexpectedly acidic nanoparticles formed in dimethylamine–ammonia–sulfuric-acid nucleation experiments at CLOUD, Atmos. Chem. Phys., 16, 13601–13618, https://doi.org/10.5194/acp-16-13601-2016, 2016.
Lee, S.-H., Uin, J., Guenther, A. B., Gouw, J. A. d., Yu, F., Nadykto, A.
B., Herb, J., Ng, N. L., Koss, A., Brune, W. H., Baumann, K., Kanawad, V.
P., Keutsch, F. N., Nenes, A., Olsen, K., Goldstein, A., and Qi, O.:
Isoprene suppression of new particle formation: Potential mechanism and
implications, J. Geophys. Res., 121, 14621–14635,
10.1029/2016JD024844, 2016.
Lee, S.-H., Gordon, H., Yu, H., Lehtipalo, K., Haley, R., Li, Y., and Zhang, R.: New particle formation in the atmosphere: From molecular clusters to global climate, J. Geophys. Res., 124, https://doi.org/10.1029/2018JD029356, online first, 2019.
Lehtipalo, K., Leppä, J., Kontkanen, J., Kangasluoma, J., Franchin, A.,
Wimmer, D., Schobesberger, S., Junninen, H., Petäjä, T., Sipilä,
M., Mikkilä, J., Vanhanen, J., Worsnop, D. R., and Kulmala, M.: Methods
for determining particle size distribution and growth rates between 1 and 3 nm using the Particle Size Magnifier, Boreal Environ. Res., 19, 215–236,
2014.
Lehtipalo, K., Rondo, L., Kontkanen, J., Schobesberger, S., Jokinen, T.,
Sarnela, N., Kürten, A., Ehrhart, S., Franchin, A., Nieminen, T.,
Riccobono, F., Sipilä, M., Yli-Juuti, T., Duplissy, J., Adamov, A.,
Ahlm, L., Almeida, J., Amorim, A., Bianchi, F., Breitenlechner, M., Dommen,
J., Downard, A. J., Dunne, E. M., Flagan, R. C., Guida, R., Hakala, J.,
Hansel, A., Jud, W., Kangasluoma, J., Kerminen, V.-M., Keskinen, H., Kim,
J., Kirkby, J., Kupc, A., Kupiainen-Määttä, O., Laaksonen, A.,
Lawler, M. J., Leiminger, M., Mathot, S., Olenius, T., Ortega, I. K.,
Onnela, A., Petäjä, T., Praplan, A., Rissanen, M. P., Ruuskanen, T.,
Santos, F. D., Schallhart, S., Schnitzhofer, R., Simon, M., Smith, J. N.,
Tröstl, J., Tsagkogeorgas, G., Tomé, A., Vaattovaara, P.,
Vehkamäki, H., Vrtala, A. E., Wagner, P. E., Williamson, C., Wimmer, D.,
Winkler, P. M., Virtanen, A., Donahue, N. M., Carslaw, K. S., Baltensperger,
U., Riipinen, I., Curtius, J., Worsnop, D. R., and Kulmala, M.: The effect
of acid–base clustering and ions on the growth of atmospheric
nano-particles, Nat. Commun., 7, 11594, https://doi.org/10.1038/ncomms11594, 2016.
Lehtipalo, K., Yan, C., Dada, L., Bianchi, F., Xiao, M., Wagner, R.,
Stolzenburg, D., Ahonen, L. R., Amorim, A., Baccarini, A., Bauer, P. S.,
Baumgartner, B., Bergen, A., Bernhammer, A.-K., Breitenlechner, M., Brilke,
S., Buchholz, A., Mazon, S. B., Chen, D., Chen, X., Dias, A., Dommen, J.,
Draper, D. C., Duplissy, J., Ehn, M., Finkenzeller, H., Fischer, L., Frege,
C., Fuchs, C., Garmash, O., Gordon, H., Hakala, J., He, X., Heikkinen, L.,
Heinritzi, M., Helm, J. C., Hofbauer, V., Hoyle, C. R., Jokinen, T.,
Kangasluoma, J., Kerminen, V.-M., Kim, C., Kirkby, J., Kontkanen, J.,
Kürten, A., Lawler, M. J., Mai, H., Mathot, S., Mauldin, R. L., Molteni,
U., Nichman, L., Nie, W., Nieminen, T., Ojdanic, A., Onnela, A., Passananti,
M., Petäjä, T., Piel, F., Pospisilova, V., Quéléver, L. L.
J., Rissanen, M. P., Rose, C., Sarnela, N., Schallhart, S., Schuchmann, S.,
Sengupta, K., Simon, M., Sipilä, M., Tauber, C., Tomé, A.,
Tröstl, J., Väisänen, O., Vogel, A. L., Volkamer, R., Wagner, A.
C., Wang, M., Weitz, L., Wimmer, D., Ye, P., Ylisirniö, A., Zha, Q.,
Carslaw, K. S., Curtius, J., Donahue, N. M., Flagan, R. C., Hansel, A.,
Riipinen, I., Virtanen, A., Winkler, P. M., Baltensperger, U., Kulmala, M.,
and Worsnop, D. R.: Multicomponent new particle formation from sulfuric
acid, ammonia, and biogenic vapors, J. Sci. Adv., 4, eaau5363, https://doi.org/10.1126/sciadv.aau5363,
2018.
Lovejoy, E. R., Curtius, J., and Froyd, K. D.: Atmospheric ion-induced
nucleation of sulfuric acid and water J. Geophys. Res., 109, D08204, https://doi.org/10.1029/2003JD004460, 2004.
Malila, J., McGraw, R., Laaksonen, A., and Lehtinen, K. E. J.: Repairing the
first nucleation theorem: Precritical cluster losses, AIP Conf. Proc., 1527, 31–34, https://doi.org/10.1063/1.4803197, 2013.
Martin, S. T., Artaxo, P., Machado, L., Manzi, A. O., Souza, R. A. F.,
Schumacher, C., Wang, J., Biscaro, T., Brito, J., Calheiros, A., Jardine,
K., Medeiros, A., Portela, B., de Sá, S. S., Adachi, K., Aiken, A. C.,
Albrecht, R., Alexander, L., Andreae, M. O., Barbosa, H. M. J., Buseck, P.,
Chand, D., Comstock, J. M., Day, D. A., Dubey, M., Fan, J., Fast, J., Fisch,
G., Fortner, E., Giangrande, S., Gilles, M., Goldstein, A. H., Guenther, A.,
Hubbe, J., Jensen, M., Jimenez, J. L., Keutsch, F. N., Kim, S., Kuang, C.,
Laskin, A., McKinney, K., Mei, F., Miller, M., Nascimento, R., Pauliquevis,
T., Pekour, M., Peres, J., Petäjä, T., Pöhlker, C., Pöschl,
U., Rizzo, L., Schmid, B., Shilling, J. E., Dias, M. A. S., Smith, J. N.,
Tomlinson, J. M., Tóta, J., and Wendisch, M.: The Green Ocean Amazon
Experiment (GoAmazon2014/5) Observes Pollution Affecting Gases, Aerosols,
Clouds, and Rainfall over the Rain Forest, B. Am.
Meteorol. Soc., 98, 981–997, https://doi.org/10.1175/BAMS-D-15-00221.1, 2016.
McGraw, R. and Zhang, R.: Multivariate analysis of homogeneous nucleation
rate measurements, Nucleation in the p-toluic acid/sulfuric acid/water
system, J. Chem. Phys., 128, 064508, https://doi.org/10.1063/1.2830030,
2008.
Merikanto, J., Spracklen, D. V., Mann, G. W., Pickering, S. J., and Carslaw, K. S.: Impact of nucleation on global CCN, Atmos. Chem. Phys., 9, 8601–8616, https://doi.org/10.5194/acp-9-8601-2009, 2009.
Nieminen, T., Paasonen, P., Manninen, H. E., Sellegri, K., Kerminen, V.-M., and Kulmala, M.: Parameterization of ion-induced nucleation rates based on ambient observations, Atmos. Chem. Phys., 11, 3393–3402, https://doi.org/10.5194/acp-11-3393-2011, 2011.
Petäjä, T., Mauldin III, R. L., Kosciuch, E., McGrath, J., Nieminen, T., Paasonen, P., Boy, M., Adamov, A., Kotiaho, T., and Kulmala, M.: Sulfuric acid and OH concentrations in a boreal forest site, Atmos. Chem. Phys., 9, 7435–7448, https://doi.org/10.5194/acp-9-7435-2009, 2009.
Raes, F.: Entrainment of free tropospheric aerosols as a regulating
mechanism for cloud condensation nuclei in the remote marine boundary layer, J. Geophys. Res.-Atmos.,
100, 2893–2903, https://doi.org/10.1029/94jd02832, 1995.
Russell, L. M., Pandis, S. N., and Seinfeld, J. H.: Aerosol production and
growth in the marine boundary layer, J. Geophys. Res.-Atmos., 99, 20989–21003, https://doi.org/10.1029/94jd01932, 1994.
Schobesberger, S., Franchin, A., Bianchi, F., Rondo, L., Duplissy, J., Kürten, A., Ortega, I. K., Metzger, A., Schnitzhofer, R., Almeida, J., Amorim, A., Dommen, J., Dunne, E. M., Ehn, M., Gagné, S., Ickes, L., Junninen, H., Hansel, A., Kerminen, V.-M., Kirkby, J., Kupc, A., Laaksonen, A., Lehtipalo, K., Mathot, S., Onnela, A., Petäjä, T., Riccobono, F., Santos, F. D., Sipilä, M., Tomé, A., Tsagkogeorgas, G., Viisanen, Y., Wagner, P. E., Wimmer, D., Curtius, J., Donahue, N. M., Baltensperger, U., Kulmala, M., and Worsnop, D. R.: On the composition of ammonia–sulfuric-acid ion clusters during aerosol particle formation, Atmos. Chem. Phys., 15, 55–78, https://doi.org/10.5194/acp-15-55-2015, 2015.
Seinfeld, J. H. and Pandis, S. N.: Atmospheric chemistry and physics: From
air pollution to climate change, John Wiley and Sons, Inc., New Jersey,
2016.
Skrabalova, L., Brus, D., Anttila, T., Zdimal, V., and Lihavainen, H.: Growth of sulphuric acid nanoparticles under wet and dry conditions, Atmos. Chem. Phys., 14, 6461–6475, https://doi.org/10.5194/acp-14-6461-2014, 2014.
Stangl, C. M., Krasnomowitz, J. M., Apsokardu, M. J., Tiszenkel, L., Ouyang,
Q., Lee, S., and Johnston, M. V.: Sulfur Dioxide Modifies Aerosol Particle
Formation and Growth by Ozonolysis of Monoterpenes and Isoprene, J. GEophys. Res.-Atmos., 124,
4800–4811, https://doi.org/10.1029/2018jd030064, 2019.
Stolzenburg, D., Fischer, L., Vogel, A. L., Heinritzi, M., Schervish, M.,
Simon, M., Wagner, A. C., Dada, L., Ahonen, L. R., Amorim, A., Baccarini,
A., Bauer, P. S., Baumgartner, B., Bergen, A., Bianchi, F., Breitenlechner,
M., Brilke, S., Mazon, S. B., Chen, D. X., Dias, A., Draper, D. C.,
Duplissy, J., Haddad, I., Finkenzeller, H., Frege, C., Fuchs, C., Garmash,
O., Gordon, H., He, X., Helm, J., Hofbauer, V., Hoyle, C. R., Kim, C.,
Kirkby, J., Kontkanen, J., Kuerten, A., Lampilahti, J., Lawler, M.,
Lehtipalo, K., Leiminger, M., Mai, H., Mathot, S., Mentler, B., Molteni, U.,
Nie, W., Nieminen, T., Nowak, J. B., Ojdanic, A., Onnela, A., Passananti,
M., Petaja, T., Quelever, L. L. J., Rissanen, M. P., Sarnela, N.,
Schallhart, S., Tauber, C., Tome, A., Wagner, R., Wang, M., Weitz, L.,
Wimmer, D., Xiao, M., Yan, C., Ye, P., Zha, Q., Baltensperger, U., Curtius,
J., Dommen, J., Flagan, R. C., Kulmala, M., Smith, J. N., Worsnop, D. R.,
Hansel, A., Donahue, N. M., and Winkler, P. M.: Rapid growth of organic
aerosol nanoparticles over a wide tropospheric temperature range, P.
Natl. Acad. Sci. USA, 115, 9122–9127, https://doi.org/10.1073/pnas.1807604115, 2018.
Tröstl, J., Chuang, W. K., Gordon, H., Heinritzi, M., Yan, C., Molteni,
U., Ahlm, L., Frege, C., Bianchi, F., Wagner, R., Simon, M., Lehtipalo, K.,
Williamson, C., Craven, J. S., Duplissy, J., Adamov, A., Almeida, J.,
Bernhammer, A.-K., Breitenlechner, M., Brilke, S., Dias, A., Ehrhart, S.,
Flagan, R. C., Franchin, A., Fuchs, C., Guida, R., Gysel, M., Hansel, A.,
Hoyle, C. R., Jokinen, T., Junninen, H., Kangasluoma, J., Keskinen, H., Kim,
J., Krapf, M., Kürten, A., Laaksonen, A., Lawler, M., Leiminger, M.,
Mathot, S., Möhler, O., Nieminen, T., Onnela, A., Petäjä, T.,
Piel, F. M., Miettinen, P., Rissanen, M. P., Rondo, L., Sarnela, N.,
Schobesberger, S., Sengupta, K., Sipilä, M., Smith, J. N., Steiner, G.,
Tomè, A., Virtanen, A., Wagner, A. C., Weingartner, E., Wimmer, D.,
Winkler, P. M., Ye, P., Carslaw, K. S., Curtius, J., Dommen, J., Kirkby, J.,
Kulmala, M., Riipinen, I., Worsnop, D. R., Donahue, N. M., and
Baltensperger, U.: The role of low-volatility organic compounds in initial
particle growth in the atmosphere, Nature, 533, 527–531, https://doi.org/10.1038/nature18271, 2016.
Vanhanen, J., Mikkila, J., Lehtipalo, K., Sipila, M., Manninen, H. E.,
Siivola, E., Petaja, T., and Kulmala, M.: Particle size magnifier for
nano-CN detection, Aerosol Sci. Tech., 45, 533–542, https://doi.org/10.1080/02786826.2010.547889, 2011.
Varanda Rizzo, L., Roldin, P., Brito, J., Backman, J., Swietlicki, E., Krejci, R., Tunved, P., Petäjä, T., Kulmala, M., and Artaxo, P.: Multi-year statistical and modeling analysis of submicrometer aerosol number size distributions at a rain forest site in Amazonia, Atmos. Chem. Phys., 18, 10255–10274, https://doi.org/10.5194/acp-18-10255-2018, 2018.
Vehkamäki, H., Kulmala, M., Napari, I., Lehtinen, E. J., Timmreck, C., Noppel, M., and Laaksonen, A.: An improved parameterization for sulfuric acid-water nucleation rates for tropospheric and stratospheric conditions, J. Geophys. Res., 107, D22, https://doi.org/10.1029/2002JD002184, 2002.
Vehkamäki, H., McGrath, M. J., Kurtén, T., Julin, J., Lehtinen, K.
E. J., and Kulmala, M.: Rethinking the application of the first nucleation
theorem to particle formation, J. Chem. Phys., 136, 094107, https://doi.org/10.1063/1.3689227, 2012.
Wang, J., Krejci, R., Giangrande, S., Kuang, C., Barbosa, H. M. J., Brito,
J., Carbone, S., Chi, X., Comstock, J., Ditas, F., Lavric, J., Manninen, H.
E., Mei, F., Moran-Zuloaga, D., Pöhlker, C., Pöhlker, M. L.,
Saturno, J., Schmid, B., Souza, R. A. F., Springston, S. R., Tomlinson, J.
M., Toto, T., Walter, D., Wimmer, D., Smith, J. N., Kulmala, M., Machado, L.
A. T., Artaxo, P., Andreae, M. O., Petäjä, T., and Martin, S. T.:
Amazon boundary layer aerosol concentration sustained by vertical transport
during rainfall, Nature, 539, 416–419, https://doi.org/10.1038/nature19819, 2016.
Wang, M. and Penner, J. E.: Aerosol indirect forcing in a global model with particle nucleation, Atmos. Chem. Phys., 9, 239–260, https://doi.org/10.5194/acp-9-239-2009, 2009.
Yao, L., Garmash, O., Bianchi, F., Zheng, J., Yan, C., Kontkanen, J.,
Junninen, H., Mazon, S. B., Ehn, M., Paasonen, P., Sipila, M., Wang, M. Y.,
Wang, X. K., Xiao, S., Chen, H. F., Lu, Y. Q., Zhang, B. W., Wang, D. F.,
Fu, Q. Y., Geng, F. H., Li, L., Wang, H. L., Qiao, L. P., Yang, X., Chen, J.
M., Kerminen, V. M., Petaja, T., Worsnop, D. R., Kulmala, M., and Wang, L.:
Atmospheric new particle formation from sulfuric acid and amines in a
Chinese megacity, Science, 361, 278–281, https://doi.org/10.1126/science.aao4839, 2018.
You, Y., Kanawade, V. P., de Gouw, J. A., Guenther, A. B., Madronich, S., Sierra-Hernández, M. R., Lawler, M., Smith, J. N., Takahama, S., Ruggeri, G., Koss, A., Olson, K., Baumann, K., Weber, R. J., Nenes, A., Guo, H., Edgerton, E. S., Porcelli, L., Brune, W. H., Goldstein, A. H., and Lee, S.-H.: Atmospheric amines and ammonia measured with a chemical ionization mass spectrometer (CIMS), Atmos. Chem. Phys., 14, 12181–12194, https://doi.org/10.5194/acp-14-12181-2014, 2014.
Young, L. H., Benson, D. R., Kameel, F. R., Pierce, J. R., Junninen, H., Kulmala, M., and Lee, S.-H.: Laboratory studies of H2SO4∕H2O binary homogeneous nucleation from the SO2+OH reaction: evaluation of the experimental setup and preliminary results, Atmos. Chem. Phys., 8, 4997–5016, https://doi.org/10.5194/acp-8-4997-2008, 2008.
Yu, F. and Luo, G.: Simulation of particle size distribution with a global aerosol model: contribution of nucleation to aerosol and CCN number concentrations, Atmos. Chem. Phys., 9, 7691–7710, https://doi.org/10.5194/acp-9-7691-2009, 2009.
Yu, F., Luo, G., Pryor, S. C., Pillai, P. R., Lee, S. H., Ortega, J., Schwab, J. J., Hallar, A. G., Leaitch, W. R., Aneja, V. P., Smith, J. N., Walker, J. T., Hogrefe, O., and Demerjian, K. L.: Spring and summer contrast in new particle formation over nine forest areas in North America, Atmos. Chem. Phys., 15, 13993–14003, https://doi.org/10.5194/acp-15-13993-2015, 2015.
Yu, H. and Lee, S. H.: A chemical ionization mass spectrometer for the
detection of atmospheric amines, Environ. Chem., 9, 190–201, 2012.
Yu, H., McGraw, R., and Lee, S. H.: Effects of amines on formation of sub-3
nm particles and their subsequent growth, Geophys. Res. Lett., 39, L02807, https://doi.org/10.1029/2011gl050099, 2012.
Yu, H., Dai, L., Zhao, Y., Kanawade, V. P., Tripathi, S. N., Ge, X., Chen,
M., and Lee, S.-H.: Laboratory observations of temperature and humidity
dependencies of nucleation and growth rates of sub-3 nm particles, J.
Geophys. Res., 122, 1919–1929, https://doi.org/10.1002/2016JD025619, 2017a.
Yu, H., Ren, L., and Kanawade, V. P.: New Particle Formation and Growth
Mechanisms in Highly Polluted Environments, Current Pollution Reports, 3,
245–253, https://doi.org/10.1007/s40726-017-0067-3, 2017b.
Zhang, R., Khalizov, A. F., Wang, L., Hu, M., and Xu, W.: Nucleation and
growth of nanoparticles in the atmosphere, Chem. Rev., 112, 957–2011, 2012.
Zollner, J. H., Glasoe, W. A., Panta, B., Carlson, K. K., McMurry, P. H., and Hanson, D. R.: Sulfuric acid nucleation: power dependencies, variation with relative humidity, and effect of bases, Atmos. Chem. Phys., 12, 4399–4411, https://doi.org/10.5194/acp-12-4399-2012, 2012.
Short summary
Understanding the processes surrounding the formation and growth of atmospheric aerosol particles is essential for understanding their effects on air quality, human health and cloud formation. Current atmospheric models neglect many essential variables that influence these processes. This study investigates temperature effects on new particle formation and the formation of clusters and their subsequent growth in differing temperature conditions.
Understanding the processes surrounding the formation and growth of atmospheric aerosol...
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