Source apportionment of PM2.5 in the southeastern United States using solvent-extractable organic compounds as tracers

被引:441
|
作者
Zheng, M [1 ]
Cass, GR
Schauer, JJ
Edgerton, ES
机构
[1] Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30332 USA
[2] Univ Wisconsin, Wisconsin State Lab Hyg, Environm Chem & Technol Program, Madison, WI 53706 USA
[3] Atmospher Res & Anal Inc, Cary, NC 27513 USA
关键词
D O I
10.1021/es011275x
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A chemical mass balance (CMB) receptor model using particle-phase organic compounds as tracers is applied to apportion the primary source contributions to fine particulate matter and fine particulate organic carbon concentrations in the southeastern United States to determine the seasonal variability of these concentrations. Source contributions to particles with aerodynamic diameter less than or equal to2.5 mum (PM2.5) collected from four urban and four rural/suburban sites in AL, FL, GA, and MS during April, July, and October 1999 and January 2000 are calculated and presented. Organic compounds in monthly composite samples at each site are identified and quantified by gas chromatography/mass spectrometry and are used as molecular markers in the CMB model. The major contributors to identified PM2.5 organic carbon concentrations at these sites in the southeastern United States include wood combustion (25-66%), diesel exhaust (14-30%), meat cooking (5-12%), and gasoline-powered motor vehicle exhaust(0-10%), as well as smaller but statistically significant contributions from natural gas combustion, paved road dust, and vegetative detritus. The primary sources determined in the present study when added to secondary aerosol formation account for on average 89% of PM2.5 mass concentrations, with the major contributors to PM2.5 mass as secondary sulfate (30 +/- 6%), wood combustion (15 +/- 12%), diesel exhaust (16 +/- 7%), secondary ammonium (8 +/- 2%), secondary nitrate (4 +/- 3%), meat cooking (3 2%), gasoline-powered motor vehicle exhaust (2 +/- 2%), and road dust (2 +/- 2%). Distinct seasonality is observed in source contributions, including higher contributions from wood combustion during the colder months of October and January. In addition, higher percentages of unexplained fine organic carbon concentrations are observed in July, which are likely due to an increase in secondary organic aerosol formation during the summer season.
引用
收藏
页码:2361 / 2371
页数:11
相关论文
共 50 条
  • [1] Source apportionment of PM2.5 in the southeastern United States using solvent-extractable organic compounds as tracers
    Sch. of Earth/Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA 30332, United States
    [J]. Environ. Sci. Technol., 1600, 11 (2361-2371):
  • [2] Background PM2.5 source apportionment in the remote Northwestern United States
    Hadley, Odelle L.
    [J]. ATMOSPHERIC ENVIRONMENT, 2017, 167 : 298 - 308
  • [3] Characterization of the solvent extractable organic compounds in PM2.5 aerosols in Hong Kong
    Zheng, M
    Fang, M
    Wang, F
    To, KL
    [J]. ATMOSPHERIC ENVIRONMENT, 2000, 34 (17) : 2691 - 2702
  • [4] Source apportionment of PM2.5 in Shanghai based on hourly organic molecular markers and other source tracers
    Li, Rui
    Wang, Qiongqiong
    He, Xiao
    Zhu, Shuhui
    Zhang, Kun
    Duan, Yusen
    Fu, Qingyan
    Qiao, Liping
    Wang, Yangjun
    Huang, Ling
    Li, Li
    Yu, Jian Zhen
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2020, 20 (20) : 12047 - 12061
  • [5] Polar organic oxygenates in PM2.5 at a southeastern site in the United States
    Edney, EO
    Kleindienst, TE
    Conver, TS
    McIver, CD
    Corse, EW
    Weathers, WS
    [J]. ATMOSPHERIC ENVIRONMENT, 2003, 37 (28) : 3947 - 3965
  • [6] Source apportionment of PM2.5:: Comparing PMF and CMB results for four ambient monitoriniz sites in the southeastern United States
    Lee, Sangil
    Liu, Wei
    Wang, Yuhang
    Russell, Armistead G.
    Edgerton, Eric S.
    [J]. ATMOSPHERIC ENVIRONMENT, 2008, 42 (18) : 4126 - 4137
  • [7] PM2.5 source apportionment with organic markers in the Southeastern Aerosol Research and Characterization (SEARCH) study
    Watson, John G.
    Chow, Judith C.
    Lowenthal, Douglas H.
    Chen, L. -W. Antony
    Shaw, Stephanie
    Edgerton, Eric S.
    Blanchard, Charles L.
    [J]. JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2015, 65 (09) : 1104 - 1118
  • [8] Reactive oxygen species associated with water-soluble PM2.5 in the southeastern United States: spatiotemporal trends and source apportionment
    Verma, V.
    Fang, T.
    Guo, H.
    King, L.
    Bates, J. T.
    Peltier, R. E.
    Edgerton, E.
    Russell, A. G.
    Weber, R. J.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2014, 14 (23) : 12915 - 12930
  • [9] Impact of meteorology and energy structure on solvent extractable organic compounds of PM2.5 in Beijing, China
    Feng, JL
    Chan, CK
    Fang, M
    Hu, M
    He, LY
    Tang, XY
    [J]. CHEMOSPHERE, 2005, 61 (05) : 623 - 632
  • [10] Estimates of future PM2.5 levels in southeastern united states
    Odman, MT
    Boylan, JW
    Russell, AG
    [J]. AIR POLLUTION MODELING AND ITS APPLICATION XVI, 2004, 16 : 163 - 170