环境化学
气溶胶
煤燃烧产物
微粒
化学
无机离子
总有机碳
煤
有机质
燃烧
化学成分
质量浓度(化学)
质谱法
环境科学
离子
色谱法
物理化学
有机化学
作者
Zhaolian Ye,Qing Li,Jiashu Liu,Shipeng Luo,Quanfa Zhou,Chenglu Bi,Shuaishuai Ma,Yanfang Chen,Hui Chen,Ling Li,Xinlei Ge
出处
期刊:Chemosphere
[Elsevier]
日期:2017-05-17
卷期号:183: 176-185
被引量:38
标识
DOI:10.1016/j.chemosphere.2017.05.094
摘要
Mass concentrations and chemical compositions of submicron particles (PM1) collected during July 2015 to April 2016 in Changzhou, a city in the Yangtze River Delta region, were systematically investigated for the first time. Specifically, an Aerodyne soot particle aerosol mass spectrometer (SP-AMS) was employed to characterize the water-soluble organic matter (WSOM). The average concentration of PM1 was 63.6 μg m-3, occupying ∼60% of co-collected PM2.5 mass. Water soluble inorganic ions (WSIIs) was the most abundant component with secondary ions (SO42-, NO3- and NH4+) as the dominant species. Organic matter (OM) accounted for 21.6% of PM1, with approximately 80% was water-soluble. Trace metals could constitute up to 3.0% of PM1 mass, and Fe, Al and Zn were the three most abundant ones. PAHs were predominated by ones with 5-6 rings, occupying over half of the PAHs mass; further analyses showed that fuel and coal combustion had significant contributions to PAHs. Positive matrix factorization of the WSOM data separated four factors: a traffic-related hydrocarbon-like OA (HOA), a local OA (LOA) likely associated with cooking and coal combustion emissions, etc., a secondary nitrogen-enriched OA (NOA) and an oxygenated OA (OOA). PCA analyses showed that crustal source was likely important for PM1 too. Back trajectory results implied that both PM1 and PM2.5 were mainly derived from local/regional emissions. Our findings present results regarding the PM1 chemistry and its relationship with the PM2.5 in Changzhou, which are valuable for the government to make effective policies to reduce the aerosol pollution in and near the city.
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