Measurement of nonvolatile particle number size distribution

被引:20
作者
Gkatzelis, G. I. [1 ,2 ]
Papanastasiou, D. K. [1 ,2 ]
Florou, K. [1 ,2 ]
Kaltsonoudis, C. [1 ,2 ]
Louvaris, E. [1 ,2 ]
Pandis, S. N. [1 ,2 ,3 ]
机构
[1] ICE HT, Inst Chem Engn Sci, Patras, Greece
[2] Univ Patras, Dept Chem Engn, GR-26110 Patras, Greece
[3] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
关键词
AEROSOL MASS-SPECTROMETER; ORGANIC AEROSOL; AIR-POLLUTION; BROWN CARBON; BLACK CARBON; VOLATILITY; AMBIENT; THERMODENUDER; FRACTIONS; ABSORPTION;
D O I
10.5194/amt-9-103-2016
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
An experimental methodology was developed to measure the nonvolatile particle number concentration using a thermodenuder (TD). The TD was coupled with a high-resolution time-of-flight aerosol mass spectrometer, measuring the chemical composition and mass size distribution of the submicrometer aerosol and a scanning mobility particle sizer (SMPS) that provided the number size distribution of the aerosol in the range from 10 to 500 nm. The method was evaluated with a set of smog chamber experiments and achieved almost complete evaporation (> 98 %) of secondary organic as well as freshly nucleated particles, using a TD temperature of 400 degrees C and a centerline residence time of 15 s. This experimental approach was applied in a winter field campaign in Athens and provided a direct measurement of number concentration and size distribution for particles emitted from major pollution sources. During periods in which the contribution of biomass burning sources was dominant, more than 80% of particle number concentration remained after passing through the thermodenuder, suggesting that nearly all biomass burning particles had a nonvolatile core. These remaining particles consisted mostly of black carbon (60% mass contribution) and organic aerosol (OA; 40 %). Organics that had not evaporated through the TD were mostly biomass burning OA (BBOA) and oxygenated OA (OOA) as determined from AMS source apportionment analysis. For periods during which traffic contribution was dominant 50-60% of the particles had a nonvolatile core while the rest evaporated at 400 degrees C. The remaining particle mass consisted mostly of black carbon with an 80% contribution, while OA was responsible for another 15-20 %. Organics were mostly hydrocarbon-like OA (HOA) and OOA. These results suggest that even at 400 degrees C some fraction of the OA does not evaporate from particles emitted from com-mon combustion processes, such as biomass burning and car engines, indicating that a fraction of this type of OA is of extremely low volatility.
引用
收藏
页码:103 / 114
页数:12
相关论文
共 46 条
[1]   Aerosol volatility measurement using an improved thermodenuder: Application to secondary organic aerosol [J].
An, Woo Jin ;
Pathak, Ravi K. ;
Lee, Byong-Hyoek ;
Pandis, Spyros N. .
JOURNAL OF AEROSOL SCIENCE, 2007, 38 (03) :305-314
[2]   Black carbon or brown carbon?: The nature of light-absorbing carbonaceous aerosols [J].
Andreae, M. O. ;
Gelencser, A. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2006, 6 :3131-3148
[3]   OH clock determination by proton transfer reaction mass spectrometry at an environmental chamber [J].
Barmet, P. ;
Dommen, J. ;
DeCarlo, P. F. ;
Tritscher, T. ;
Praplan, A. P. ;
Platt, S. M. ;
Prevot, A. S. H. ;
Donahue, N. M. ;
Baltensperger, U. .
ATMOSPHERIC MEASUREMENT TECHNIQUES, 2012, 5 (03) :647-656
[4]   Actinometric measurements of NO2 photolysis frequencies in the atmosphere simulation chamber SAPHIR [J].
Bohn, B ;
Rohrer, F ;
Brauers, T ;
Wahner, A .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 :493-503
[5]   Bounding the role of black carbon in the climate system: A scientific assessment [J].
Bond, T. C. ;
Doherty, S. J. ;
Fahey, D. W. ;
Forster, P. M. ;
Berntsen, T. ;
DeAngelo, B. J. ;
Flanner, M. G. ;
Ghan, S. ;
Kaercher, B. ;
Koch, D. ;
Kinne, S. ;
Kondo, Y. ;
Quinn, P. K. ;
Sarofim, M. C. ;
Schultz, M. G. ;
Schulz, M. ;
Venkataraman, C. ;
Zhang, H. ;
Zhang, S. ;
Bellouin, N. ;
Guttikunda, S. K. ;
Hopke, P. K. ;
Jacobson, M. Z. ;
Kaiser, J. W. ;
Klimont, Z. ;
Lohmann, U. ;
Schwarz, J. P. ;
Shindell, D. ;
Storelvmo, T. ;
Warren, S. G. ;
Zender, C. S. .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2013, 118 (11) :5380-5552
[6]   Separation of volatile and non-volatile aerosol fractions by thermodesorption:: instrumental development and applications [J].
Burtscher, H ;
Baltensperger, U ;
Bukowiecki, N ;
Cohn, P ;
Hüglin, C ;
Mohr, M ;
Matter, U ;
Nyeki, S ;
Schmatloch, V ;
Streit, N ;
Weingartner, E .
JOURNAL OF AEROSOL SCIENCE, 2001, 32 (04) :427-442
[7]   Chemical and microphysical characterization of ambient aerosols with the aerodyne aerosol mass spectrometer [J].
Canagaratna, M. R. ;
Jayne, J. T. ;
Jimenez, J. L. ;
Allan, J. D. ;
Alfarra, M. R. ;
Zhang, Q. ;
Onasch, T. B. ;
Drewnick, F. ;
Coe, H. ;
Middlebrook, A. ;
Delia, A. ;
Williams, L. R. ;
Trimborn, A. M. ;
Northway, M. J. ;
DeCarlo, P. F. ;
Kolb, C. E. ;
Davidovits, P. ;
Worsnop, D. R. .
MASS SPECTROMETRY REVIEWS, 2007, 26 (02) :185-222
[8]   Quantitative estimates of the volatility of ambient organic aerosol [J].
Cappa, C. D. ;
Jimenez, J. L. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2010, 10 (12) :5409-5424
[9]   The global burden of disease due to outdoor air pollution [J].
Cohen, AJ ;
Anderson, HR ;
Ostro, B ;
Pandey, KD ;
Krzyzanowski, M ;
Künzli, N ;
Gutschmidt, K ;
Pope, A ;
Romieu, I ;
Samet, JM ;
Smith, K .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2005, 68 (13-14) :1301-1307
[10]   Measurements of volatile organic compounds in the earths atmosphere using proton-transfer-reaction mass spectrometry [J].
de Gouw, Joost ;
Warneke, Carsten .
MASS SPECTROMETRY REVIEWS, 2007, 26 (02) :223-257