Chemical characteristics of size-resolved aerosols in winter in Beijing  

作　　者：Kang Sun Yu Qu Qiong Wu Tingting Han Jianwei Gu Jingjing Zhao Yele Sun Qi Jiang Ziqi Gao Min Hu Yuanhang Zhang Keding Lu Stephan Nordmann Yafang Cheng Li Hou Hui Ge Masami Furuuchi Mitsuhiko Hata Xingang Liu 

机构地区：[1]State Key Laboratory of Water Environment Simulation,School of Environment,Beijing Normal University [2]College of Environmental Sciences and Engineering,Peking University [3]State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry,Institute of Atmospheric Physics,Chinese Academy of Sciences [4]Environmental Science Center,University of Augsburg [5]School of Foreign Languages,China University of Political Science and Law [6]School of Chemistry,Beijing Normal University [7]Multiphase Chemistry Department,Max Planck Institute for Chemistry [8]Laboratory of Atmospheric Environment and Pollution Control Engineering,Graduate School of Natural Science & Technology,Kanazawa University

出　　处：《Journal of Environmental Sciences》2014年第8期1641-1650,共10页环境科学学报（英文版）

基　　金：supported by the National Natural Science Foundation of China (No.41175018);the Ministry of Science and Technology of China (No.2013CB955804);the special fund of State Key Joint Laboratory of Environment Simulation and Pollution Control (Nos.13Z02ESPCP and 13K04ESPCP)

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 PM2.5concentrations during the measurement were 150.5 ± 96.0 μg/m3（mean ± standard variation）and 106.9 ± 71.6 μg/m3,respectively. The PM2.5/PM10 ratio was 0.70 ± 0.10,indicating that PM2.5dominated PM10. The aerosol size distributions showed that three size bins of 0.5–1,1–2.5 and 2.5–10 μm 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.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 PM2.5concentrations during the measurement were 150.5 ± 96.0 μg/m3（mean ± standard variation）and 106.9 ± 71.6 μg/m3,respectively. The PM2.5/PM10 ratio was 0.70 ± 0.10,indicating that PM2.5dominated PM10. The aerosol size distributions showed that three size bins of 0.5–1,1–2.5 and 2.5–10 μm 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.

关 键 词：AEROSOL Size distribution Chemical characteristics BEIJING 

分 类 号：X513[环境科学与工程—环境工程]