Water-soluble organic carbon (WSOC), as major fractions of atmospheric aerosols, have gained attention due to their light-absorption properties. To illustrate the sources and key environmental factors driving WSOC formation under different atmospheric conditions, a comparative study was conducted by summarizing the results obtained from five field campaigns at inland (urban, suburban or regional) sites and a coastal site during different seasons. Organic carbon concentrations varied from 8.5 μg/m at the summer regional site to 17.5 μg/m at the winter urban site, with 46 %- 89 % of the mass as WSOC. Based on correlation analysis, primary combustion emissions were more important in winter than in summer, and secondary formation was an important source of WSOC during winter, summer and autumn. Atmospheric oxidants (NO, O), aerosol liquid water (ALW) and ambient RH were important factors influencing the WSOC formation, while their roles varied in different atmospheres. We observed a seasonal transition of atmospheric oxidants dominating the WSOC formation from O and NO-driven conditions in summer to NO-driven conditions in winter. Elevated ALW or ambient RH generally favor the WSOC formation, while the WSOC dependence of ALW varied among different ALW ranges. As the increasing of ALW or ambient RH, a transition of WSOC formation from "RH/ALW-limited regime" under low-ALW conditions, to "RH/ALW and precursor-driven regime" under medium-ALW/RH, and to "precursor-limited (RH/ALW-excess) regime" were observed for the inland atmospheric conditions. Under the high-RH and ALW conditions in coastal areas, ALW or ambient RH was generally not a limiting factor for WSOC formation.
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http://dx.doi.org/10.1016/j.scitotenv.2022.161364 | DOI Listing |
Environ Sci Pollut Res Int
October 2024
Department of Environmental Science and Engineering (ESED), Indian Institute of Technology Bombay, Mumbai, India.
J Environ Sci (China)
March 2025
Atmospheric Sciences Research Center, University at Albany, SUNY, Albany 12226, USA.
Environ Pollut
November 2024
Key Laboratory of Yellow River and Huai River Water Environment and Pollution Control, Ministry of Education, Henan Key Laboratory for Environmental Pollution Control, School of Environment, Henan Normal University, Xinxiang, 453007, China.
Atmospheric fine particulate matter (PM) can trigger the production of cytotoxic reactive oxygen species (ROS), which can trigger or exacerbate oxidative stress and pulmonary inflammation. We collected 111 daily (∼24 h) ambient PM samples within an urban region of North China during four seasons of 2019-2020. PM samples were examined for carbonaceous components, water-soluble ions, and elements, together with their oxidative potential (represent ROS-producing ability) by DTT assay.
View Article and Find Full Text PDFSci Total Environ
October 2024
Institute of Surface-Earth System Science, School of Earth System Science, Tianjin University, Tianjin 300072, China. Electronic address:
Sci Total Environ
October 2024
School of Metallurgy, Northeastern University, Shenyang 110819, China. Electronic address:
Inorganic nitrates were considered to be a potential source of atmospheric NO/HONO during the daytime. To better evaluate the contribution of nitrate photochemistry on NO/HONO formation, the photolysis of nitrates in the real atmospheric environment needs to be further explored. Here, the NO generation by the photolysis of inorganic nitrates in the presence of total water-soluble organic carbon (WSOC) was quantified.
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