TY - JOUR
T1 - Urban organic aerosol composition in eastern China differs from north to south
T2 - Molecular insight from a liquid chromatography-mass spectrometry (Orbitrap) study
AU - Wang, Kai
AU - Huang, Ru Jin
AU - Brüggemann, Martin
AU - Zhang, Yun
AU - Yang, Lu
AU - Ni, Haiyan
AU - Guo, Jie
AU - Wang, Meng
AU - Han, Jiajun
AU - Bilde, Merete
AU - Glasius, Marianne
AU - Hoffmann, Thorsten
N1 - Funding Information:
Acknowledgements. This study was supported by the National Natural Science Foundation of China (NSFC, grant nos. 41925015, 91644219 and 41877408), the Chinese Academy of Sciences (nos. ZDBS-LY-DQC001 and XDB40030202), the National Key Research and Development Program of China (no. 2017YFC0212701), and the German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) under grant no. INST 247/664-1 FUGG. Kai Wang and Yun Zhang acknowledge the scholarship from the Chinese Scholarship Council (CSC). Kai Wang acknowledges the scholarship from the Max Plank Graduate Center with Johannes Gutenberg University of Mainz (MPGC) and thanks Ulrich Pöschl, Christopher J. Kampf and Yafang Cheng for their helpful suggestions for this study. Kai Wang also thanks Huanfeng Dong from Zhejiang University for the great support on the programming of data processing.
Funding Information:
Financial support. This research has been supported by the Na-
Publisher Copyright:
© 2021 Kai Wang et al.
PY - 2021/6/15
Y1 - 2021/6/15
N2 - 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 ≤2.5g μm (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 non-target 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 81g %-99.7g % 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.
AB - 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 ≤2.5g μm (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 non-target 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 81g %-99.7g % 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.
UR - http://www.scopus.com/inward/record.url?scp=85108172828&partnerID=8YFLogxK
U2 - 10.5194/acp-21-9089-2021
DO - 10.5194/acp-21-9089-2021
M3 - Journal article
AN - SCOPUS:85108172828
SN - 1680-7316
VL - 21
SP - 9089
EP - 9104
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 11
ER -