Urban organic aerosol composition in eastern China differs from north to south: molecular insight from a liquid chromatography-mass spectrometry (Orbitrap) study

被引:35
|
作者
Wang, Kai [1 ,2 ,3 ,6 ]
Huang, Ru-Jin [1 ,2 ,4 ]
Brueggemand, Martin [5 ]
Zhang, Yun [3 ]
Yang, Lu [1 ,2 ]
Ni, Haiyan [1 ,2 ]
Guo, Jie [1 ,2 ]
Wang, Meng [1 ,2 ]
Han, Jiajun [7 ]
Bilde, Merete [6 ]
Glasius, Marianne [6 ]
Hoffmann, Thorsten [3 ]
机构
[1] Chinese Acad Sci, Inst Earth & Environm, Ctr Excellence Quaternary Sci & Global Change, State Key Lab Loess & Quaternary Geol SKLLQG, Xian 710061, Peoples R China
[2] Chinese Acad Sci, Inst Earth & Environm, Key Lab Aerosol Chem & Phys, Xian 710061, Peoples R China
[3] Johannes Gutenberg Univ Mainz, Inst Inorgan & Analyt Chem, Duesbergweg 10-14, D-55128 Mainz, Germany
[4] Pilot Natl Lab Marine Sci & Technol Qingdao, Open Studio Ocean Continental Climate & Environm, Qingdao 266061, Peoples R China
[5] Leibniz Inst Tropospher Res TROPOS, Atmospher Chem Dept ACD, Oserstr 1, D-04318 Leipzig, Germany
[6] Aarhus Univ, Dept Chem, Langelandsgade 140, DK-8000 Aarhus C, Denmark
[7] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
基金
中国国家自然科学基金;
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; ELECTROSPRAY-IONIZATION; SEVERE HAZE; ORGANOSULFATES; POLLUTION; CHEMISTRY; EMISSIONS; OXIDATION; FIELD;
D O I
10.5194/acp-21-9089-2021
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Air pollution by particulate matter in China affects human health, the ecosystem and the climate. However, the chemical composition of particulate aerosol, especially of the organic fraction, is still not well understood. In this study, particulate aerosol samples with a diameter of <= 2.5 mu m (PM2.5) were collected in January 2014 in three cities located in northeast, east and southeast China, namely Changchun, Shanghai and Guangzhou. Organic aerosol (OA) in the PM2.5 samples was analyzed by an ultrahigh-performance liquid chromatograph (UHPLC) coupled to a high-resolution Orbitrap mass spectrometer in both negative mode (ESI-) and positive mode electrospray ionization (ESI+). After nontarget screening including the assignment of molecular formulas, the compounds were classified into five groups based on their elemental composition, i.e., CHO, CHON, CHN, CHOS and CHONS. The CHO, CHON and CHN groups present the dominant signal abundances of 81 %-99.7 % in the mass spectra and the majority of these compounds were assigned to mono- and polyaromatics, suggesting that anthropogenic emissions are a major source of urban OA in all three cities. However, the chemical characteristics of these compounds varied between the different cities. The degree of aromaticity and the number of polyaromatic compounds were substantially higher in samples from Changchun, which could be attributed to the large emissions from residential heating (i.e., coal combustion) during wintertime in northeast China. Moreover, the ESI- analysis showed higher H/C and O/C ratios for organic compounds in Shanghai and Guangzhou compared to samples from Changchun, indicating that OA undergoes more intense photochemical oxidation processes in lower-latitude regions of China and/or is affected to a larger degree by biogenic sources. The majority of sulfur-containing compounds (CHOS and CHONS) in all cities were assigned to aliphatic compounds with low degrees of unsaturation and aromaticity. Here again, samples from Shanghai and Guangzhou show a greater chemical similarity but differ largely from those from Changchun. It should be noted that the conclusions drawn in this study are mainly based on comparison of molecular formulas weighted by peak abundance and thus are associated with inherent uncertainties due to different ionization efficiencies for different organic species.
引用
收藏
页码:9089 / 9104
页数:16
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