Source characterization of volatile organic compounds in urban Beijing and its links to secondary organic aerosol formation

被引:7
|
作者
Liu, Quan [1 ,2 ]
Sheng, Jiujiang [3 ]
Wu, Yangzhou [4 ]
Ma, Zhiqiang [5 ]
Sun, Junying [1 ,2 ]
Tian, Ping [3 ]
Zhao, Delong [3 ]
Li, Xia [3 ]
Hu, Kang [4 ]
Li, Siyuan [4 ]
Shen, Xiaojing [1 ,2 ]
Zhang, Yangmei [1 ,2 ]
He, Hui [3 ]
Huang, Mengyu [3 ,6 ]
Ding, Deping [3 ,7 ]
Liu, Dantong [4 ]
机构
[1] Chinese Acad Meteorol Sci, State Key Lab Severe Weather, Beijing 100081, Peoples R China
[2] Chinese Acad Meteorol Sci, Key Lab Atmospher Chem CMA, Beijing 100081, Peoples R China
[3] Beijing Weather Modificat Ctr, Beijing 100089, Peoples R China
[4] Zhejiang Univ, Sch Earth Sci, Dept Atmospher Sci, Hangzhou 310027, Zhejiang, Peoples R China
[5] China Meteorol Adm, Inst Urban Meteorol, Beijing 100089, Peoples R China
[6] China Meteorol Adm, Field Expt Base Cloud & Precipitat Res North Chin, Beijing 101200, Peoples R China
[7] Beijing Key Lab Cloud Precipitat & Atmospher Wate, Beijing 100089, Peoples R China
基金
中国国家自然科学基金;
关键词
VOCs; PTR-ToF-MS; Source apportionment; SOA formation; Air mass trajectories; PTR-TOF-MS; ATMOSPHERIC SUBMICRON AEROSOLS; POSITIVE MATRIX FACTORIZATION; ROAD EMISSION CHARACTERISTICS; HIGH-RESOLUTION; CHEMICAL-COMPOSITION; MASS-SPECTROMETRY; SOA FORMATION; BLACK CARBON; INORGANIC AEROSOLS;
D O I
10.1016/j.scitotenv.2022.160469
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Volatile organic compounds (VOCs) are precursors for ozone and secondary organic aerosol (SOA) formation, thereby playing a vital role in atmospheric chemistry and urban air quality. To characterize the relationship between VOCs and SOA, organics both in gas and particulate phases were concurrently measured in urban Beijing. The VOCs and organic aerosol (OA) were apportioned into factors with different oxidation levels by applying the factorization analysis on their detailed mass spectra. Six factors of VOCs were identified, including four primary VOCs (PVOC) factors and two secondary VOCs (SVOC) factors. The PVOC factors dominated the total VOCs when the air mass originated in the cleaner northern areas, while SVOC factors dominated for polluted southern air masses. The normalized concen-trations of PVOC and primary OA factors showed consistent diurnal variations regardless of air mass directions, owing to the relatively stable local emissions during the experimental period. This contrasted with the secondary fac-tors due to more complex transformation processes. The traffic-related VOCs and solid fuel combustion VOCs nega-tively correlated with SOA, implying that they may have contributed to the SOA formation through photooxidation. The VOCs in lower oxidation levels were found to have poor correlations with the less oxidized SOA, whereas they cor-related strongly to the more oxidized SOA. This implied that the less oxidized SOA may be in a transition state, where its production and loss rates were balanced. These served as products of VOCs oxidation and reactants of more oxidized SOA formation, playing important roles on the VOC to SOA transformation. The identified VOC emission sources and their photochemical production of SOA should be considered in air quality policy planning.
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页数:12
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