Identification of secondary organic aerosols based on aerosol mass spectrometry

Secondary organic aerosol (SOA) is one of the major components of aerosols in the atmosphere and has not been well understood so far. Due to the complex chemical composition of organic aerosols, the identification of SOA has been a hotspot and difficult issue in the field of aerosol study. This stud...

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Veröffentlicht in:Science China. Chemistry 2010-12, Vol.53 (12), p.2593-2599
Hauptverfasser: Huang, XiaoFeng, Zhao, QianBiao, He, LingYan, Hu, Min, Bian, QiJing, Xue, Lian, Zhang, YuanHang
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Sprache:eng
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Zusammenfassung:Secondary organic aerosol (SOA) is one of the major components of aerosols in the atmosphere and has not been well understood so far. Due to the complex chemical composition of organic aerosols, the identification of SOA has been a hotspot and difficult issue in the field of aerosol study. This study attempts to quantitatively identify SOA in winter of Shenzhen based on positive matrix factorization (PMF) analysis. Major sources were resolved and SOA was identified subsequently according to the characteristic ion fragments measured by highly time-resolved aerosol mass spectrometer measurement. It showed that in the winter of Shenzhen the average SOA concentration was 9.41 ± 6.33 μg/m 3 , accounting for 39.9 ± 21.8% of the total organic mass. Compared with primary organic aerosol (POA), the SOA concentrations had no large variation, suggestive of characteristics of regional secondary pollutants. The ratio of SOA/BC had pronounced diurnal variation, similar to that of O x (O 3 +NO 2 ), indicating SOA formation was significantly controlled by activity of photochemistry in the atmosphere. The most effective period for SOA formation was from 9 am ∼3 pm since the SOA/BC ratio increased by 122% during this period. This study provides a new technical method and a new idea for SOA investigation.
ISSN:1674-7291
1869-1870
DOI:10.1007/s11426-010-4088-7