Chemical Characteristics and Sources of Water-Soluble Organic Nitrogen Species in PM2.5 in Nanjing, China

被引:9
|
作者
Liu, Yue [1 ]
Li, Haiwei [1 ]
Cui, Shijie [1 ]
Nie, Dongyang [2 ]
Chen, Yanfang [1 ]
Ge, Xinlei [1 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Jiangsu Key Lab Atmospher Environm Monitoring & P, Collaborat Innovat Ctr Atmospher Environm & Equip, Sch Environm Sci & Engn, Nanjing 210044, Peoples R China
[2] Nanjing Univ, Sch Atmospher Sci, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
organic nitrogen; mass spectra; aqueous-phase oxidation; source apportionment; AEROSOL MASS-SPECTROMETRY; YANGTZE-RIVER DELTA; ATMOSPHERIC PARTICULATE MATTER; SOURCE APPORTIONMENT; AQUEOUS-PHASE; FINE PARTICLES; BROWN CARBON; SECONDARY; INSIGHTS; IONS;
D O I
10.3390/atmos12050574
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Water-soluble organic nitrogen (WSON) is an important component of PM2.5 which may affect air quality, climate and human health. Herein, one-year field samples of atmospheric PM2.5 (June 2017-May 2018) were collected in northern Nanjing. Chemical characterization of PM2.5 major components as well as WSON were conducted, and WSON composition and sources were further investigated via measurements by a Aerodyne soot particle aerosol mass spectrometer (SP-AMS) as well as positive matrix factorization (PMF). Inorganic ions, mainly consisting of ammonium, sulfate, and nitrate, were found to dominate PM2.5 mass (58.7%), followed by organic matter (OM) (22.6%), and elemental carbon (EC) (2.1%). Water-soluble OM dominated OM (65.1%), and its temporal variation was closely correlated with that of secondary organic matter, while time series of water-insoluble OM concentrations correlated tightly with that of primary organic matter. Average WSON concentration was 2.15 mu g/m(3), which was highest in winter and lowest in summer. Correlation analysis of WSON with PM2.5 components also indicated that WSON was mainly from secondary sources. SP-AMS revealed that WSON mass spectrum was composed of CxHyNp+ (91.2%) and CxHyOzNp+ (8.8%), indicating dominance of amines and other oxygenated ON compounds. PMF analysis resolved two primary sources (traffic, biomass burning) and two secondary sources (less-oxidized and more-oxidized factors) of WSOM and WSON, and the secondary source dominated both WSOM and WSON. Contribution of the more-oxidized ON factor was very high in winter, and the less-oxidized factor was significant in summer, indicating a likely important role of aqueous-phase processing in winter as well as photochemical oxidation in summer to WSON.
引用
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页数:18
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