4.7 Article

Winter ClNO2 formation in the region of fresh anthropogenic emissions: seasonal variability and insights into daytime peaks in northern China

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ATMOSPHERIC CHEMISTRY AND PHYSICS
卷 21, 期 20, 页码 15985-16000

出版社

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-21-15985-2021

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资金

  1. National Natural Science Foundation of China [91544213, 91844301, 41922051]
  2. Hong Kong Research Grants Council [T24-504/17-N, A-PolyU502/16]
  3. National Key Research and Development Program of China [2016YFC0200500]

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Nitryl chloride (ClNO2) is an important chlorine reservoir in the atmosphere, impacting the oxidation of volatile organic compounds (VOCs) and the production of ROx radicals and ozone (O3); this study found that winter concentrations of ClNO2 were generally lower than summer concentrations, but daytime peaks could reach up to 1.3 ppbv, significantly influencing ROx levels and daily O3 productions.
Nitryl chloride (ClNO2) is an important chlorine reservoir in the atmosphere that affects the oxidation of volatile organic compounds (VOCs) and the production of ROx radicals and ozone (O-3). This study presents measurements of ClNO2 and related compounds at urban, polluted rural, and polluted lower tropospheric (mountaintop) sites in the winter of 2017-2018 over the North China Plain (NCP). The nocturnal concentrations of ClNO2 were lower at the urban and polluted rural sites but higher at the polluted lower tropospheric site. The winter concentrations of ClNO2 were generally lower than the summer concentrations that were previously observed at these sites, which was due to the lower nitrate radical (NO3) production rate (P(NO3)) and the smaller N2O5 uptake coefficients (gamma(N2O5)) in winter, despite the higher ratios of dinitrogen pentoxide (N2O5) to NO3 in winter. Significant daytime peaks of ClNO(2 )were observed at all the sites during the winter campaigns, with ClNO2 mixing ratios of up to 1.3 ppbv. Vertical transport of ClNO2 from the residual layers and prolonged photochemical lifetime of ClNO2 in winter may explain the elevated daytime concentrations. The daytime-averaged chlorine radical (Cl) production rates (P (Cl)) from the daytime ClNO2 were 0.17, 0.11, and 0.12 ppbv h(-1) at the polluted rural, urban, and polluted lower tropospheric sites, respectively, which were approximately 3-4 times higher than the campaign-averaged conditions. Box model calculations showed that the Cl atoms liberated during the daytime peaks of ClNO2 increased the ROx levels by up to 27 %-37 % and increased the daily O-3 productions by up to 13 %-18 %. Our results provide new insights into the ClNO2 processes in the lower troposphere impacted by fresh and intense anthropogenic emissions and reveal that ClNO2 can be an important daytime source of Cl radicals under certain conditions in winter.

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