Atmospheric fate of peroxyacetyl nitrate in suburban Hong Kong and its impact on local ozone pollution

被引:42
|
作者
Zeng, Lewei [1 ]
Fan, Gang-Jie [2 ]
Lyu, Xiaopu [1 ]
Guo, Hai [1 ]
Wang, Jia-Lin [2 ]
Yao, Dawen [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Civil & Environm Engn, Air Qual Studies, Hong Kong, Peoples R China
[2] Natl Cent Univ, Dept Chem, Taoyuan, Taiwan
基金
国家重点研发计划;
关键词
Photochemical smog; Master chemical mechanism (MCM); Precursors; Formation pathways; O-3; formation; VOLATILE ORGANIC-COMPOUNDS; PEARL RIVER DELTA; MASTER CHEMICAL MECHANISM; MCM V3 PART; PEROXYPROPIONYL NITRATE; TROPOSPHERIC DEGRADATION; ACETYL NITRATE; TRACE GASES; PAN; PROTOCOL;
D O I
10.1016/j.envpol.2019.06.004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Peroxyacetyl nitrate (PAN) is an important reservoir of atmospheric nitrogen, modulating reactive nitrogen cycle and ozone (O-3) formation. To understand the origins of PAN, a field measurement was conducted at Tung Chung site (TC) in suburban Hong Kong from October to November 2016. The average level of PAN was 0.63 +/- 0.05 ppbv, with a maximum of 7.30 ppbv. Higher PAN/O-3 ratio (0.043-0.058) was captured on episodes, i.e. when hourly maximum O-3 exceeded 80 ppbv, than on non-episodes (0.01), since O-3 production was less efficient than PAN when there was an elevation of precursors (i.e. volatile organic compounds (VOCs) and nitrogen oxide (NOx)). Model simulations revealed that oxidations of acetaldehyde (65.3 +/- 2.3%), methylglyoxal (MGLY, 12.7 +/- 1.2%) and other oxygenated VOCs (OVOCs) (8.0 +/- 0.6%), and radical cycling (12.2 +/- 0.8%) were the major production pathways of peroxyacetyl (PA) radical, while local PAN formation was controlled by both VOCs and nitrogen dioxide (NO2). Among all VOC species, carbonyls made the highest contribution (59%) to PAN formation, followed by aromatics (26%) and biogenic VOCs (BVOCs) (10%) through direct oxidation/decomposition. Besides, active VOCs (i.e. carbonyls, aromatics, BVOCs and alkenes/alkynes) could stimulate hydroxyl (OH) production, thus indirectly facilitating the PAN formation. Apart from primary emissions, carbonyls were also generated from oxidation of first-generation precursors, i.e., hydrocarbons, of which xylenes contributed the most to PAN production. Furthermore, PAN formation suppressed local O-3 formation at a rate of 2.84 ppbv/ppbv, when NO2, OH and hydroperoxy (HO2) levels decreased and nitrogen monoxide (NO) value enhanced. Namely, O-3 was reduced by 2.84 ppbv per ppbv PAN formation. Net O-3 production rate was weakened (similar to 36%) due to PAN photochemistry, so as each individual production and loss pathway. The findings advanced our knowledge of atmospheric PAN and its impact on O-3 production. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1910 / 1919
页数:10
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