Parameterized atmospheric oxidation capacity and speciated OH reactivity over a suburban site in the North China Plain: A comparative study between summer and winter

被引:22
|
作者
Yang, Yuan [1 ,2 ]
Wang, Yonghong [1 ,4 ]
Huang, Wei [1 ,2 ]
Yao, Dan [1 ,2 ,3 ]
Zhao, Shuman [1 ,2 ]
Wang, Yinghong [1 ]
Ji, Dongsheng [1 ]
Zhang, Renjian [1 ]
Wang, Yuesi [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Atmospher Phys, Beijing 100029, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Inst Urban Environm, Ctr Excellence Reg Atmospher Environm, Xiamen 361021, Peoples R China
[4] Inst Atmospher & Earth Syst Res, Phys, Fac Sci, POB 64, Helsinki 00014, Finland
关键词
VOCs; AOC; Speciated OH reactivity; Photochemical pollution; Sources; North China Plain; PEARL RIVER DELTA; GAS-PHASE REACTIONS; VOLATILE ORGANIC-COMPOUNDS; MIXING LAYER HEIGHT; OZONE PRODUCTION; AIR-POLLUTION; PHOTOCHEMICAL DATA; HO2; CONCENTRATIONS; RADICAL CHEMISTRY; NITROGEN-DIOXIDE;
D O I
10.1016/j.scitotenv.2021.145264
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The atmospheric oxidation capacity (AOC) and photochemical reactivity are of increasing concern owing to their roles in photochemical pollution. The AOC and OH reactivity were evaluated based on simultaneous measurements of volatile organic compounds (VOCs), trace gases and photolysis frequency during summer and winter campaigns at a suburban site in Xianghe. The AOC exhibited well-defined seasonal and diurnal patterns, with higher intensities during the summertime and daytime than during the wintertime and nighttime, respectively. The major reductants contributing to the AOC during the summertime were CO (41%) and alkenes (41%), whereas CO (40%) and oxygenated VOCs (OVOCs) (30%) dominated the AOC during the wintertime. The dominant oxidant contributor to the AOC during the daytime was OH (>= 93%), while the contributions of O-3 and NO3 (>= 75%) to the AOC increased during the nighttime. High values during the wintertime and an increase at night were features of the speciated OH reactivity. Inorganic compounds (NOx and CO) dominated the speciated OH reactivity (76% and 85% during the summer and winter campaigns, respectively). Among VOCs, the dominant contributors were alkenes (12%) and OVOCs (7%) during the summer and winter campaigns, respectively. The ratio of NOx- and VOC-attributed OH reactivity indicated that O-3 formation occurred under a VOC-limited regime during the summertime and that aromatics had the largest potential to form O-3. Isoprene and m/p-xylene were themost important contributors to the AOC, OH reactivity and O-3-forming among VOCs during the summertime, biogenic sources and secondary formation and industrial production were the main sources of these species. During the wintertime, hexanal and ethylene were the key VOC species contributing to the AOC and OH reactivity, and solvent usage and traffic-related emissions were themain contributing sources. We recommend that priority measures for the control of VOC species and sources should be taken when suitable. Capsule: This study focused on the similarities and differences in the AOC and speciated OH reactivity during summer and winter campaigns. (C) 2021 Published by Elsevier B.V.
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页数:14
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