Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/97690
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorXia, Men_US
dc.creatorPeng, Xen_US
dc.creatorWang, Wen_US
dc.creatorYu, Cen_US
dc.creatorWang, Zen_US
dc.creatorTham, YJen_US
dc.creatorChen, Jen_US
dc.creatorChen, Hen_US
dc.creatorMu, Yen_US
dc.creatorZhang, Cen_US
dc.creatorLiu, Pen_US
dc.creatorXue, Len_US
dc.creatorWang, Xen_US
dc.creatorGao, Jen_US
dc.creatorLi, Hen_US
dc.creatorWang, Ten_US
dc.date.accessioned2023-03-09T07:42:42Z-
dc.date.available2023-03-09T07:42:42Z-
dc.identifier.issn1680-7316en_US
dc.identifier.urihttp://hdl.handle.net/10397/97690-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2021. This work is distributed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Xia, M., Peng, X., Wang, W., Yu, C., Wang, Z., Tham, Y. J., Chen, J., Chen, H., Mu, Y., Zhang, C., Liu, P., Xue, L., Wang, X., Gao, J., Li, H., and Wang, T.: Winter ClNO2 formation in the region of fresh anthropogenic emissions: seasonal variability and insights into daytime peaks in northern China, Atmos. Chem. Phys., 21, 15985–16000 is available at https://doi.org/10.5194/acp-21-15985-2021en_US
dc.titleWinter ClNO2 formation in the region of fresh anthropogenic emissions : seasonal variability and insights into daytime peaks in northern Chinaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage15985en_US
dc.identifier.epage16000en_US
dc.identifier.volume21en_US
dc.identifier.issue20en_US
dc.identifier.doi10.5194/acp-21-15985-2021en_US
dcterms.abstractNitryl 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 (O3). 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 (γ(N2O5)) in winter, despite the higher ratios of dinitrogen pentoxide (N2O5) to NO3 in winter. Significant daytime peaks of ClNO2 were observed at all the sites during the winter campaigns, with ClNO2 mixing ratios of up to 1.3ppbv. 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 0.12ppbvh-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 O3 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.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric Chemistry and Physics, Oct. 2021, v. 21, no. 20, p. 15985-16000en_US
dcterms.isPartOfAtmospheric chemistry and physicsen_US
dcterms.issued2021-10-
dc.identifier.isiWOS:000711958700001-
dc.identifier.scopus2-s2.0-85118257012-
dc.identifier.eissn1680-7324en_US
dc.description.validate202303 bcwwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China, NSFC: 41922051, 91544213, 91844301; Research Grants Councilen_US
dc.description.fundingTextUniversity Grants Committee, 研究資助局: A-PolyU502/16, T24-504/17-N; National Key Research and Development Program of China, NKRDPC: 2016YFC0200500en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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