Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/103524
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dc.contributorDepartment of Civil and Environmental Engineeringen_US
dc.creatorYuan, Qen_US
dc.creatorZhang, Zen_US
dc.creatorChen, Yen_US
dc.creatorHui, Len_US
dc.creatorWang, Men_US
dc.creatorXia, Men_US
dc.creatorZou, Zen_US
dc.creatorWei, Wen_US
dc.creatorHo, KFen_US
dc.creatorWang, Zen_US
dc.creatorLai, Sen_US
dc.creatorZhang, Yen_US
dc.creatorWang, Ten_US
dc.creatorLee, Sen_US
dc.date.accessioned2023-12-12T07:33:43Z-
dc.date.available2023-12-12T07:33:43Z-
dc.identifier.issn0048-9697en_US
dc.identifier.urihttp://hdl.handle.net/10397/103524-
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.titleOrigin and transformation of volatile organic compounds at a regional background site in Hong Kong : varied photochemical processes from different source regionsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume908en_US
dc.identifier.doi10.1016/j.scitotenv.2023.168316en_US
dcterms.abstractVolatile organic compounds (VOCs) are important gaseous constituents in the troposphere, impacting local and regional air quality, human health, and climate. Oxidation of VOCs, with the participation of nitrogen oxides (NOx), leads to the formation of tropospheric ozone (O3). Accurately apportioning the emission sources and transformation processes of ambient VOCs, and effectively estimation of OH reactivity and ozone formation potential (OFP) will play an important role in reducing O3 pollution in the atmosphere and improving public health. In this study, field measurements were conducted at a regional background site (Hok Tsui; HT) in Hong Kong from October to November 2020 with proton-transfer-reaction time-of-flight mass spectrometry (PTR-ToF-MS). VOC data coupled with air mass back trajectory cluster analysis and receptor modelling were applied to reveal the pollution pattern, emission sources and transformation of ambient VOCs at HT in autumn 2020. Seven sources were identified by positive matrix factorization (PMF) analysis, namely vehicular + industrial, solvent usage, primary oxygenated VOCs (OVOCs), secondary OVOCs 1, secondary OVOCs 2 (aged), biogenic emissions, and background + biomass burning. Secondary formation and vehicular + industrial emissions are the vital sources of ambient VOCs at HT supersite, contributing to 20.8 % and 46.7 % of total VOC mixing ratios, respectively. Integrated with backward trajectory analysis and correlations of VOCs with their oxidation products, short-range transport of air masses from inland regions of southeast China brought high levels of total VOCs but longer-range transport of air masses brought more secondary OVOCs in aged air masses. Photolysis of OVOCs was the most important contributor to OH reactivity and OFP, among which aldehyde was the dominant contributor. The results of this study highlight the photochemical processing of VOCs from different source regions which should be considered in strategy making for pollution reduction.en_US
dcterms.accessRightsembargoed accessen_US
dcterms.bibliographicCitationScience of the total environment, 15 Jan. 2024, v. 908, 168316en_US
dcterms.isPartOfScience of the total environmenten_US
dcterms.issued2024-01-15-
dc.identifier.eissn1879-1026en_US
dc.identifier.artn168316en_US
dc.description.validate202312 bcchen_US
dc.description.oaNot applicableen_US
dc.identifier.FolderNumbera2535-
dc.identifier.SubFormID47830-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.date.embargo2026-01-15en_US
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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Embargo End Date 2026-01-15
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