Secondary organic aerosol formation in China from urban-lifestyle sources: Vehicle exhaust and cooking emission

被引:10
|
作者
Zhang, Zirui [1 ]
Zhu, Wenfei [1 ]
Hu, Min [1 ]
Wang, Hui [1 ]
Tang, Lizi [1 ]
Hu, Shuya [1 ]
Shen, Ruizhe [1 ]
Yu, Ying [1 ]
Song, Kai [1 ]
Tan, Rui [1 ]
Chen, Zheng [1 ]
Chen, Shiyi [1 ]
Canonaco, Francesco [2 ,3 ]
Prevot, Andre S. H. [2 ]
Guo, Song [1 ]
机构
[1] Peking Univ, Coll Environm Sci & Engn, State Key Joint Lab Environm Simulat & Pollut Con, Int Joint Lab Reg Pollut Control,Minist Educ IJRC, Beijing 100871, Peoples R China
[2] Paul Scherrer Inst PSI, Lab Atmospher Chem, CH-5232 Villigen, Switzerland
[3] Datalystica Ltd, Pk InnovAARE, CH-5234 Villigen, Switzerland
基金
中国国家自然科学基金;
关键词
Urban air pollution; Anthropogenic activities; Source apportionment; Aerosol mass spectrometry (AMS); Field observation; Laboratory simulation; NEW-YORK-CITY; MASS-SPECTROMETER; SOURCE APPORTIONMENT; SEASONAL-VARIATIONS; SUBMICRON AEROSOLS; TOF-AMS; EVOLUTION; OXIDATION; ME-2; COMPONENTS;
D O I
10.1016/j.scitotenv.2022.159340
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
An increasing number of people tend to live in cities, where they suffer from serious air pollution from anthropogenic sources. Vehicle exhaust and cooking emission are closely related to daily life of urban residents, and could be defined as "urban-lifestyle sources". The primary emissions of urban-lifestyle sources tend to form abundant secondary organic aerosols (SOA) through complicated atmospheric chemistry processes. The newly formed SOA is a kind of complex mixture and causes considerable health effects with high uncertainty. Most studies focus on formation pathway, mass growth potential and chemical feature of urban-lifestyle SOA under simple laboratory conditions. Few studies have measured the urban-lifestyle SOA in ambient air, let alone verified laboratory findings under complicated atmo-spheric conditions. In this work, we established a new method that combined laboratory simulation and field observa-tion, which quantified the urban-lifestyle SOA with high time resolution under the real atmospheric condition. The complex SOA was measured and resolved by a high-resolution time-of -flight aerosol mass spectrometer (HR-ToF-AMS). The multilinear engine model (ME-2) and multilinear correction methods were used to apply laboratory results into ambient SOA apportionment. It was found that the vehicle source dominated the SOA formation during the diur-nal photochemical process, and the SOA:POA ratio of vehicle source was about 1.4 times larger than that of cooking source. The vehicle emission may undergo an alcohol/peroxide & carboxylic acid oxidation pathway and form higher oxidized SOA, while the cooking emission may undergo an alcohol/peroxide oxidation pathway and form relatively lower oxidized SOA. The vehicle SOA and cooking SOA contributed 45.6 % and 24.8 % of OA during a local episode in 2021 winter of downtown Beijing. Our findings could not only provide a new way to quantify urban SOA but also demonstrate some laboratory hypotheses, conducing to understand its ambient contributions, chemical features, and environmental effects.
引用
收藏
页数:8
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