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  Measurement report: Vertical distribution of atmospheric particulate matter within the urban boundary layer in southern China - size-segregated chemical composition and secondary formation through cloud processing and heterogeneous reactions

Zhou, S., Wu, L., Guo, J., Chen, W., Wang, X., Zhao, J., et al. (2020). Measurement report: Vertical distribution of atmospheric particulate matter within the urban boundary layer in southern China - size-segregated chemical composition and secondary formation through cloud processing and heterogeneous reactions. Atmospheric Chemistry and Physics, 20(11), 6435-6453. doi:10.5194/acp-20-6435-2020.

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Zhou, Shengzhen1, Autor
Wu, Luolin1, Autor
Guo, Junchen1, Autor
Chen, Weihua1, Autor
Wang, Xuemei1, Autor
Zhao, Jun1, Autor
Cheng, Yafang2, Autor           
Huang, Zuzhao1, Autor
Zhang, Jinpu1, Autor
Sun, Yele1, Autor
Fu, Pingqing1, Autor
Jia, Shiguo1, Autor
Tao, Jun1, Autor
Chen, Yanning1, Autor
Kuang, Junxia1, Autor
Affiliations:
1external, ou_persistent22              
2Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826290              

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 Zusammenfassung: Many studies have recently been done on understanding the sources and formation mechanisms of atmospheric aerosols at ground level. However, vertical profiles and sources of size-resolved particulate matter within the urban boundary layer are still lacking. In this study, vertical distribution characteristics of size-segregated particles were investigated at three observation platforms (ground level, 118 m, and 488 m) on the 610 m high Canton Tower in Guangzhou, China. Size-segregated aerosol samples were simultaneously collected at the three levels in autumn and winter. Major aerosol components, including water-soluble ions, organic carbon, and elemental carbon, were measured. The results showed that daily average fine-particle concentrations generally decreased with height. Concentrations of sulfate and ammonium in fine particles displayed shallow vertical gradients, and nitrate concentrations increased with height in autumn, while the chemical components showed greater variations in winter than in autumn. The size distributions of sulfate and ammonium in both seasons were characterized by a dominant unimodal mode with peaks in the size range of 0.44–1.0 µm. In autumn, the nitrate size distribution was bimodal, peaking at 0.44–1.0 and 2.5–10 µm, while in winter it was unimodal, implying that the formation mechanisms for nitrate particles were different in the two seasons. Our results suggest that the majority of the sulfate and nitrate is formed from aqueous-phase reactions, and we attribute coarse-mode nitrate formation at the measurement site to the heterogeneous reactions of gaseous nitric acid on existing sea-derived coarse particles in autumn. Case studies further showed that atmospheric aqueous-phase and heterogeneous reactions could be important mechanisms for sulfate and nitrate formation, which, in combination with adverse weather conditions such as temperature inversion and calm wind, led to haze formation during autumn and winter in the Pearl River Delta (PRD) region.

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Sprache(n): eng - English
 Datum: 2020-06-04
 Publikationsstatus: Erschienen
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 Art der Begutachtung: -
 Identifikatoren: ISI: 000538544400001
DOI: 10.5194/acp-20-6435-2020
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Titel: Atmospheric Chemistry and Physics
  Kurztitel : ACP
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Göttingen : Copernicus Publications
Seiten: - Band / Heft: 20 (11) Artikelnummer: - Start- / Endseite: 6435 - 6453 Identifikator: ISSN: 1680-7316
CoNE: https://pure.mpg.de/cone/journals/resource/111030403014016