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Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
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Volume 9, issue 21
Atmos. Chem. Phys., 9, 8573–8585, 2009
https://doi.org/10.5194/acp-9-8573-2009
© Author(s) 2009. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 9, 8573–8585, 2009
https://doi.org/10.5194/acp-9-8573-2009
© Author(s) 2009. This work is distributed under
the Creative Commons Attribution 3.0 License.

  12 Nov 2009

12 Nov 2009

Source apportionment of fine organic aerosols in Beijing

Q. Wang, M. Shao, Y. Zhang, Y. Wei, M. Hu, and S. Guo Q. Wang et al.
  • State Joint Key Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, China

Abstract. Fine particles (PM2.5, i.e., particles with an aerodynamic diameter of ≤2.5 μm) were collected from the air in August 2005, August–September 2006, and January–February 2007, in Beijing, China. The chemical compositions of particulate organic matter in the ambient samples were quantified by gas chromatography/mass spectrometry. The dominant compounds identified in summertime were n-alkanoic acids, followed by dicarboxylic acids and sugars, while sugars became the most abundant species in winter, followed by polycyclic aromatic hydrocarbons, n-alkanes, and n-alkanoic acids. The contributions of seven emission sources (i.e., gasoline/diesel vehicles, coal burning, wood/straw burning, cooking, and vegetative detritus) to particulate organic matter in PM2.5 were estimated using a chemical mass balance receptor model. The model results present the seasonal trends of source contributions to organic aerosols. Biomass burning (straw and wood) had the highest contribution in winter, followed by coal burning, vehicle exhaust, and cooking. The contribution of cooking was the highest in summer, followed by vehicle exhaust and biomass burning, while coal smoke showed only a minor contribution to ambient organic carbon.

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