Characterization and source apportionment of organic aerosol using offline aerosol mass spectrometry

被引:95
|
作者
Daellenbach, K. R. [1 ]
Bozzetti, C. [1 ]
Krepelova, A. K. [1 ]
Canonaco, F. [1 ]
Wolf, R. [1 ]
Zotter, P. [1 ,7 ]
Fermo, P. [5 ]
Crippa, M. [1 ,8 ]
Slowik, J. G. [1 ]
Sosedova, Y. [1 ]
Zhang, Y. [1 ,2 ,3 ,4 ,9 ]
Huang, R. -J. [1 ]
Poulain, L. [6 ]
Szidat, S. [2 ,3 ]
Baltensperger, U. [1 ]
El Haddad, I. [1 ]
Prevot, A. S. H. [1 ]
机构
[1] Paul Scherrer Inst, Lab Atmospher Chem, CH-5232 Villigen, Switzerland
[2] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[3] Univ Bern, Oeschger Ctr Climate Change Res, CH-3012 Bern, Switzerland
[4] Paul Scherrer Inst, Lab Radiochem & Environm Chem, CH-5232 Villigen, Switzerland
[5] Univ Milan, Dept Chem, I-20133 Milan, Italy
[6] Leibniz Inst Tropospharenforsch, Leipzig, Germany
[7] Lucerne Univ Appl Sci & Arts, Lucerne Sch Engn & Architecture, Bioenergy Res, CH-6048 Horw, Switzerland
[8] Inst Environm & Sustainabil, EC Joint Res Ctr, I-21027 Ispra, Italy
[9] Nanjing Univ Informat Sci & Technol, Yale NUIST Ctr Atmospher Environm, Nanjing 10044, Jiangsu, Peoples R China
关键词
POSITIVE MATRIX FACTORIZATION; CHEMICAL-COMPOSITION; HIGH-RESOLUTION; PARTICULATE MATTER; MULTILINEAR ENGINE; ELEMENTAL CARBON; WINTERTIME; URBAN; COMPONENTS; PARTICLES;
D O I
10.5194/amt-9-23-2016
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Field deployments of the Aerodyne Aerosol Mass Spectrometer (AMS) have significantly advanced real-time measurements and source apportionment of non-refractory particulate matter. However, the cost and complex maintenance requirements of the AMS make its deployment at sufficient sites to determine regional characteristics impractical. Furthermore, the negligible transmission efficiency of the AMS inlet for supermicron particles significantly limits the characterization of their chemical nature and contributing sources. In this study, we utilize the AMS to characterize the water-soluble organic fingerprint of ambient particles collected onto conventional quartz filters, which are routinely sampled at many air quality sites. The method was applied to 256 particulate matter (PM) filter samples (PM1, PM2.5, and PM10, i.e., PM with aerodynamic diameters smaller than 1, 2.5, and 10 mu m, respectively), collected at 16 urban and rural sites during summer and winter. We show that the results obtained by the present technique compare well with those from co-located online measurements, e.g., AMS or Aerosol Chemical Speciation Monitor (ACSM). The bulk recoveries of organic aerosol (60-91 %) achieved using this technique, together with low detection limits (0.8 mu g of organic aerosol on the analyzed filter fraction) allow its application to environmental samples. We will discuss the recovery variability of individual hydrocarbon ions, ions containing oxygen, and other ions. The performance of such data in source apportionment is assessed in comparison to ACSM data. Recoveries of organic components related to different sources as traffic, wood burning, and secondary organic aerosol are presented. This technique, while subjected to the limitations inherent to filter-based measurements (e.g., filter artifacts and limited time resolution) may be used to enhance the AMS capabilities in measuring size-fractionated, spatially resolved longterm data sets.
引用
收藏
页码:23 / 39
页数:17
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