Chemical characteristics of size-resolved aerosols in winter in Beijing

被引:24
|
作者
Sun, Kang [1 ,6 ]
Qu, Yu [2 ]
Wu, Qiong [1 ]
Han, Tingting [1 ]
Gu, Jianwei [3 ]
Zhao, Jingjing [4 ]
Sun, Yele [2 ]
Jiang, Qi [2 ]
Gao, Ziqi [5 ]
Hu, Min [6 ]
Zhang, Yuanhang [6 ]
Lu, Keding [6 ]
Nordmann, Stephan [7 ]
Cheng, Yafang [6 ]
Hou, Li [8 ]
Ge, Hui [8 ]
Furuuchi, Masami [8 ]
Hata, Mitsuhiko [8 ]
Liu, Xingang [1 ]
机构
[1] Beijing Normal Univ, Sch Environm, State Key Lab Water Environm Simulat, Beijing 100875, Peoples R China
[2] Chinese Acad Sci, Inst Atmospher Phys, State Key Lab Atmospher Boundary Layer Phys & Atm, Beijing 100029, Peoples R China
[3] Univ Augsburg, Ctr Environm Sci, D-86159 Augsburg, Germany
[4] China Univ Polit Sci & Law, Sch Foreign Languages, Beijing 100088, Peoples R China
[5] Beijing Normal Univ, Sch Chem, Beijing 100875, Peoples R China
[6] Peking Univ, Coll Environm Sci & Engn, Beijing 100871, Peoples R China
[7] Max Planck Inst Chem, Multiphase Chem Dept, D-55128 Mainz, Germany
[8] Kanazawa Univ, Lab Atmospher Environm & Pollut Control Engn, Grad Sch Nat Sci & Technol, Kanazawa, Ishikawa 9201167, Japan
基金
中国国家自然科学基金;
关键词
Aerosol; Size distribution; Chemical characteristics; Beijing; ATMOSPHERIC PARTICULATE POLLUTANTS; SOURCE APPORTIONMENT; PM2.5; CHINA; SUMMER; DISTRIBUTIONS; SCATTERING; PARTICLES; URBAN; PM10;
D O I
10.1016/j.jes.2014.06.004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Size-resolved aerosols were continuously collected by a Nano Sampler for 13 days at an urban site in Beijing during winter 2012 to measure the chemical composition of ambient aerosol particles. Data collected by the Nano Sampler and an ACSM (Aerodyne Aerosol Chemical Speciation Monitor) were compared. Between the data sets, similar trends and strong correlations were observed, demonstrating the validity of the Nano Sampler. PM10 and PM2.5 concentrations during the measurement were 150.5 +/- 96.0 mu g/m(3) (mean +/- standard variation) and 106.9 +/- 71.6 mu g/m(3), respectively. The PM2.5/PM10 ratio was 0.70 +/- 0.10, indicating that PM2.5 dominated PM10. The aerosol size distributions showed that three size bins of 0.5-1, 1-2.5 and 2.5-10 mu m contributed 21.8%, 23.3% and 26.0% to the total mass concentration (TMC), respectively. OM (organic matter) and SIA (secondary ionic aerosol, mainly SO42-, NO3- and NH4+) were major components of PM2.5. Secondary compounds (SIA and secondary organic carbon) accounted for half of TMC (about 49.8%) in PM2.5, and suggested that secondary aerosols significantly contributed to the serious particulate matter pollution observed in winter. Coal burning, biomass combustion, vehicle emissions and SIA were found to be the main sources of PM2.5. Mass concentrations of water-soluble ions and undetected materials, as well as their fractions in TMC, strikingly increased with deteriorating particle pollution conditions, while OM and EC (elemental carbon) exhibited different variations, with mass concentrations slightly increasing but fractions in TMC decreasing. (C) 2014 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
引用
收藏
页码:1641 / 1650
页数:10
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