Highly time- and size-resolved characterization of submicron aerosol particles in Beijing using an Aerodyne Aerosol Mass Spectrometer

被引:198
作者
Sun, Junying [1 ]
Zhang, Qi [2 ]
Canagaratna, Manjula R. [3 ]
Zhang, Yangmei
Ng, Nga L. [3 ]
Sun, Yele [2 ]
Jayne, John T. [3 ]
Zhang, Xiaochun [1 ]
Zhang, Xiaoye [1 ]
Worsnop, Douglas R. [3 ]
机构
[1] Chinese Acad Meteorol Sci, Key Lab Atmospher Chem, Ctr Atmosphere Watch & Serv, China Meteorol Adm, Beijing 100081, Peoples R China
[2] SUNY Albany, ASRC, Albany, NY 12203 USA
[3] Aerodyne Res Inc, Ctr Aerosol & Cloud Chem, Billerica, MA 01821 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Fine particles; Primary Organic Aerosol (POA); Secondary Organic Aerosol (SOA); Megacity; Air pollution; Size distribution; Aerosol sources and processes; POSITIVE MATRIX FACTORIZATION; OXYGENATED ORGANIC AEROSOLS; EMISSION INVENTORY; HYDROCARBON-LIKE; AIR-POLLUTION; CHINA; PARTICULATE; URBAN; SPECTRA; CITIES;
D O I
10.1016/j.atmosenv.2009.03.020
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Atmospheric aerosols are a major pollutant in Beijing-a megacity in China. To achieve a better understanding of the characteristics, sources and processes of aerosols in Beijing, an Aerodyne Aerosol Mass Spectrometer (AMS) was deployed at an urban site in July 2006 to obtain size-resolved chemical composition of non-refractory submicron particles (NR-PM(1)) at 5 min resolution. During this study, NR-PM(1) was on average composed of 25% sulfate, 22% nitrate, 16% ammonium, 1.4% chloride and 35% of organic aerosol (OA) species. The average size distributions of sulfate, nitrate and ammonium were very similar and characterized by a prominent accumulation mode peaking at D(va) approximate to 600 nm. The average size distribution of OA was significantly broader due to the presence of an ultrafine mode. Multivariate analysis of the AMS organic spectra with Positive Matrix Factorization (PMF) identified a hydrocarbon-like OA (HOA) and two oxygenated OA (OOA) components. The HOA component likely corresponded to primary OA material associated with combustion-related emissions. The two ODA components, which likely corresponded to more oxidized (ODA I) and less oxidized (ODA II) secondary OA materials, accounted for 45 +/- 16% and 16 +/- 7.2%, respectively, of the observed OA mass. ODA I correlated well with sulfate while OOA II correlated well with nitrate. The particle loading, composition and size distributions observed during this campaign were highly variable. Backtrajectory analysis indicates that this variability correlated with the varying impacts of regional and local sources and processes. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:131 / 140
页数:10
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