臭氧
环境化学
空气质量指数
空气污染
对流层
氮氧化物
化学
挥发性有机化合物
气团(太阳能)
环境科学
污染
对流层臭氧
大气科学
气象学
燃烧
生态学
物理
有机化学
边界层
生物
热力学
地质学
作者
Qi Yuan,Zhuozhi Zhang,Yi Chen,Lirong Hui,Meng Wang,Men Xia,Zhouxing Zou,Wei Wan,Kin‐Fai Ho,Zhe Wang,Senchao Lai,Yingyi Zhang,Tao Wang,Shuncheng Lee
标识
DOI:10.1016/j.scitotenv.2023.168316
摘要
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.
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