Atmos. Chem. Phys., 12, 1811-1822, 2012
www.atmos-chem-phys.net/12/1811/2012/
doi:10.5194/acp-12-1811-2012
© Author(s) 2012. This work is distributed
under the Creative Commons Attribution 3.0 License.
The characteristics and origins of carbonaceous aerosol at a rural site of PRD in summer of 2006
W. W. Hu1, M. Hu1, Z. Q. Deng1, R. Xiao1, Y. Kondo2, N. Takegawa3, Y. J. Zhao4, S. Guo1, and Y. H. Zhang1
1State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871, China
2Department of Earth and Planetary Science, Graduate School of Science, University of Tokyo, Tokyo, Japan
3Research Center for Advanced Science and Technology, University of Tokyo, Tokyo, Japan
4Air Quality Research Center, University of California, Davis, CA 95616, USA

Abstract. Both organic carbon (OC) and elemental carbon (EC) were measured during PRIDE-PRD 2006 summer campaign by using a semi-continuous thermal-optical carbon analyzer at a rural site, Back Garden (BG), which is located 50 km to the northwest of Guangzhou City. Together with the online EC/OC analyzer, various kinds of instruments related to aerosol chemical properties were employed here, which provided a good opportunity to check data quality. The concentrations of OC correlated well with the mass of organic matter (OM) and water soluble organic carbon (WSOC), implying the reliability of the data measured in this campaign. The average OC concentrations in fine particle for three typical periods during the campaign (local emission influence, typhoon and precipitation and normal days) were 28.1 μgC m−3, 4.0 μgC m−3 and 5.7 μgC m−3, respectively; and EC were 11.6 μgC m−3, 1.8 μgC m−3, and 3.3 μgC m−3, respectively. The diurnal patterns of EC and OC during the campaign were higher at night and in early morning than daytime, which was probably caused by the primary emission and accumulation in the occurrence of low boundary layer. Compared with the constant diurnal enhancement ratios of EC, the enhancement ratio of OC (OC versus (CO-CObackground)) kept in a relative high level in the afternoon, with a similar diurnal profile to oxygenated organic aerosol (OOA), due to the strong photochemical formation of OC. Here, a modified EC tracer method was used to estimate the formation of secondary organic carbon (SOC). These results showed that the average SOC concentration (normal days) at BG site was about 2.0 ± 2.3 μgC m−3, and the SOC fraction in OC could reach up to 80% with the average of 47%. The modified approach in this study proved to be effective and reliable for SOC estimation based on good correlations between estimated SOC versus OOA or WSOC, and estimated POC versus hydrocarbon-like organic aerosol (HOA).

Citation: Hu, W. W., Hu, M., Deng, Z. Q., Xiao, R., Kondo, Y., Takegawa, N., Zhao, Y. J., Guo, S., and Zhang, Y. H.: The characteristics and origins of carbonaceous aerosol at a rural site of PRD in summer of 2006, Atmos. Chem. Phys., 12, 1811-1822, doi:10.5194/acp-12-1811-2012, 2012.
 
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