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DOI | 10.1016/j.atmosenv.2020.118093 |
Impact of long-range atmospheric transport on volatile organic compounds and ozone photochemistry at a regional background site in central China | |
Lei X.; Cheng H.; Peng J.; Jiang H.; Lyu X.; Zeng P.; Wang Z.; Guo H. | |
发表日期 | 2021 |
ISSN | 1352-2310 |
卷号 | 246 |
英文摘要 | Ozone (O3) photochemistry in remote areas can be altered by the injection of long-range transported air masses which contain volatile organic compounds (VOCs) and nitrogen oxides (NOx). In this study, VOCs and trace gases (i.e., SO2, NO, NO2, CO, and O3) were measured in summer (August) and autumn (October) in 2018 at Jinsha (JSH), a regional background station in central China. A unique pattern that most short-lived VOCs species presented higher mixing ratios in summer while long-lived VOCs showed higher mixing ratios in autumn was observed. Backward trajectory analysis revealed that higher mixing ratios of long-lived hydrocarbons were mostly associated with air masses originating from northern China, while lower concentrations related to air masses passed over southeastern China and the East China Sea. An observation-constrained photochemical box model coupled with Master Chemical Mechanism (PBM-MCM) was applied to simulate the net ozone production. It was found that the net ozone production rate in summer (average: 4.7 ± 0.8 ppbv/h) was higher than that in autumn (average: 2.5 ± 0.1 ppbv/h). O3 formation at JSH switched from transition regime in summer to VOC-constrained regime in autumn due to the high level of NOx in autumn. The relative incremental reactivity (RIR) analysis showed the isoprene was the most reactive VOC species to in-situ O3 production. These findings highlight the impact of long-range air pollution transport on background O3 photochemistry in central China. © 2020 |
关键词 | Central ChinaLong-range atmospheric transportOzone photochemistryRegional background siteVOCs |
语种 | 英语 |
scopus关键词 | Air pollution; Chemical reactions; Mixing; Nitrogen oxides; Ozone; Sulfur dioxide; Volatile organic compounds; Air pollution transport; Backward trajectory analysis; Long-range atmospheric transports; Master chemical mechanism; Ozone production; Photochemical box model; Southeastern china; Transition regimes; Atmospheric movements; benzene; cobalt; ethane; fossil fuel; hydrocarbon; isoprene; molybdenum; nitric oxide; oxygen; ozone; propane; sodium peroxide; volatile organic compound; air mass; concentration (composition); measurement method; mixing ratio; nitrogen oxides; ozone; photochemistry; pollutant transport; trace gas; volatile organic compound; aerosol; atmosphere; atmospheric transport; autumn; China; comparative study; controlled study; flame ionization detection; limit of detection; optical depth; photochemistry; priority journal; quality control; seasonal variation; solar radiation; summer; textile industry; topography; uncertainty; East China Sea; Pacific Ocean |
来源期刊 | ATMOSPHERIC ENVIRONMENT
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/248704 |
作者单位 | School of Resource and Environmental Sciences, Wuhan University, Wuhan, China; Air Quality Studies, Department of Civil and Environmental Engineering, Hong Kong Polytechnic University, China |
推荐引用方式 GB/T 7714 | Lei X.,Cheng H.,Peng J.,et al. Impact of long-range atmospheric transport on volatile organic compounds and ozone photochemistry at a regional background site in central China[J],2021,246. |
APA | Lei X..,Cheng H..,Peng J..,Jiang H..,Lyu X..,...&Guo H..(2021).Impact of long-range atmospheric transport on volatile organic compounds and ozone photochemistry at a regional background site in central China.ATMOSPHERIC ENVIRONMENT,246. |
MLA | Lei X.,et al."Impact of long-range atmospheric transport on volatile organic compounds and ozone photochemistry at a regional background site in central China".ATMOSPHERIC ENVIRONMENT 246(2021). |
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