Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/111586
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dc.contributorDepartment of Civil and Environmental Engineering-
dc.creatorDai, J-
dc.creatorWang, T-
dc.creatorShen, H-
dc.creatorXia, M-
dc.creatorSun, W-
dc.creatorBrasseur, GP-
dc.date.accessioned2025-03-03T06:02:30Z-
dc.date.available2025-03-03T06:02:30Z-
dc.identifier.issn0013-936X-
dc.identifier.urihttp://hdl.handle.net/10397/111586-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2025 American Chemical Societyen_US
dc.rightsThis article is licensed under CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/)en_US
dc.rightsThe following publication Dai, J., Wang, T., Shen, H., Xia, M., Sun, W., & Brasseur, G. P. (2025). Significant Impact of a Daytime Halogen Oxidant on Coastal Air Quality. Environmental Science & Technology, 59(4), 2169-2180 is available at https://doi.org/10.1021/acs.est.4c08360.en_US
dc.subjectAir pollutionen_US
dc.subjectAtmospheric oxidationen_US
dc.subjectMolecular chlorineen_US
dc.subjectWRF-Chemen_US
dc.titleSignificant impact of a daytime halogen oxidant on coastal air qualityen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage2169-
dc.identifier.epage2180-
dc.identifier.volume59-
dc.identifier.issue4-
dc.identifier.doi10.1021/acs.est.4c08360-
dcterms.abstractChlorine radicals (Cl·) are highly reactive and affect the fate of air pollutants. Several field studies in China have revealed elevated levels of daytime molecular chlorine (Cl2), which, upon photolysis, release substantial amounts of Cl· but are poorly represented in current chemical transport models. Here, we implemented a parametrization for the formation of daytime Cl2 through the photodissociation of particulate nitrate in acidic environments into a regional model and assessed its impact on coastal air quality during autumn in South China. The model could reproduce over 70% of the high Cl2 level measured at a coastal site, revealing a discernible presence of Cl2 and released Cl· in coastal and adjacent areas. Abundant Cl2 alters the oxidative capacity of the atmosphere, consequently increasing O3 (6–12%) and PM2.5 (10–16%) concentrations in high-NOx areas and reducing O3 (3%) concentration in low-NOx areas. Accounting for chlorine chemistry shifts the O3 – precursor relationships from VOC limited to mixed or NOx -limited regimes, enhancing the benefits of NOx emission reduction in mitigating O3 pollution. Our findings suggest that tightening emission control for two acidic pollutants, NOx and SO2, would alleviate reactive Cl· production and its adverse impact on air quality.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationEnvironmental science & technology, 4 Feb. 2025, v. 59, no. 4, p. 2169-2180-
dcterms.isPartOfEnvironmental science and technology-
dcterms.issued2025-02-04-
dc.identifier.scopus2-s2.0-85216178667-
dc.identifier.eissn1520-5851-
dc.description.validate202503 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TAen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Science Foundation of China (NSFC); Hong Kong Scholars Programen_US
dc.description.pubStatusPublisheden_US
dc.description.TAACS (2025)en_US
dc.description.oaCategoryTAen_US
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