Origin and transformation of volatile organic compounds at a regional background site in Hong Kong : Varied photochemical processes from different source regions
Copyright © 2023. Published by Elsevier B.V..
Volatile 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.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 2023 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:908 |
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Enthalten in: |
The Science of the total environment - 908(2023) vom: 15. Jan., Seite 168316 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Yuan, Qi [VerfasserIn] |
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Date Revised 25.11.2023 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
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doi: |
10.1016/j.scitotenv.2023.168316 |
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PPN (Katalog-ID): |
NLM364407883 |
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520 | |a Volatile 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 | ||
650 | 4 | |a Journal Article | |
700 | 1 | |a Zhang, Zhuozhi |e verfasserin |4 aut | |
700 | 1 | |a Chen, Yi |e verfasserin |4 aut | |
700 | 1 | |a Hui, Lirong |e verfasserin |4 aut | |
700 | 1 | |a Wang, Meng |e verfasserin |4 aut | |
700 | 1 | |a Xia, Men |e verfasserin |4 aut | |
700 | 1 | |a Zou, Zhouxing |e verfasserin |4 aut | |
700 | 1 | |a Wei, Wan |e verfasserin |4 aut | |
700 | 1 | |a Ho, Kin Fai |e verfasserin |4 aut | |
700 | 1 | |a Wang, Zhe |e verfasserin |4 aut | |
700 | 1 | |a Lai, Senchao |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Yingyi |e verfasserin |4 aut | |
700 | 1 | |a Wang, Tao |e verfasserin |4 aut | |
700 | 1 | |a Lee, Shuncheng |e verfasserin |4 aut | |
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