Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117059
DC FieldValueLanguage
dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.contributorUniversity Research Facility in Life Sciencesen_US
dc.creatorJiang, Yen_US
dc.creatorChen, Xen_US
dc.creatorZong, Zen_US
dc.creatorShen, Hen_US
dc.creatorSo, PKen_US
dc.creatorWang, Cen_US
dc.creatorXue, Len_US
dc.creatorWang, Xen_US
dc.creatorWang, Ten_US
dc.date.accessioned2026-01-30T00:53:42Z-
dc.date.available2026-01-30T00:53:42Z-
dc.identifier.urihttp://hdl.handle.net/10397/117059-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAir qualityen_US
dc.subjectBrominesen_US
dc.subjectChemical modelingen_US
dc.subjectOxidantsen_US
dc.subjectPharmaceutical industryen_US
dc.titleA previously unrecognized industrial source of atmospheric molecular bromine in eastern Chinaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1516en_US
dc.identifier.epage1522en_US
dc.identifier.volume12en_US
dc.identifier.issue11en_US
dc.identifier.doi10.1021/acs.estlett.5c00570en_US
dcterms.abstractReactive bromine species play an important role in atmospheric oxidation, the ozone budget, and mercury transformation, yet their abundance and sources outside polar regions remain poorly characterized. Here we report measurements of episodic plumes of molecular bromine (Br2) in a high-tech industrial park in eastern China, with mixing ratios up to 23.4 ppt at night. The alignment of wind direction of high Br2 mixing ratios with the location of the pharmaceutical facilities, along with strong correlations with brominated organics and methylating agents, suggests pharmaceutical processes as the probable source. The elevated Br2 occasionally persisted after sunrise, contributing approximately 20% to the oxidation of isoprene in the morning. Based on national bromine consumption data and conservative emission factors, we estimate that Br2 emissions from the pharmaceutical industry could rival those from residential coal combustion by 2030. These findings highlight a previously unrecognized industrial source of reactive bromine with potentially significant implications for regional air quality.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationEnvironmental science and technology letters, 11 Nov. 2025, v. 12, no. 11, p. 1516-1522en_US
dcterms.isPartOfEnvironmental science and technology lettersen_US
dcterms.issued2025-11-11-
dc.identifier.eissn2328-8930en_US
dc.description.validate202601 bcchen_US
dc.description.oaNot applicableen_US
dc.identifier.FolderNumberG000931/2026-01, a4288-n01, a4294-
dc.identifier.SubFormID52549-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2026-10-28en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2026-10-28
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