Aerosol analysis using a Thermal-Desorption Proton-Transfer-Reaction Mass Spectrometer (TD-PTR-MS): a new approach to study processing of organic aerosols

被引:73
作者
Holzinger, R. [1 ]
Williams, J. [2 ]
Herrmann, F. [2 ]
Lelieveld, J. [2 ]
Donahue, N. M. [3 ]
Rockmann, T. [1 ]
机构
[1] Inst Marine & Atmospher Res Utrecht, NL-3584 CC Utrecht, Netherlands
[2] Max Planck Inst Chem, D-55128 Mainz, Germany
[3] Carnegie Mellon Univ, Ctr Atmospher Particle Studies, Pittsburgh, PA 15213 USA
关键词
ONLINE ANALYSIS; HIGH-RESOLUTION; SECONDARY; PHOTOOXIDATION; ATMOSPHERE; INSTRUMENT; EVOLUTION; ISOPRENE; SPECTRA; TOLUENE;
D O I
10.5194/acp-10-2257-2010
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We present a novel analytical approach to measure the chemical composition of organic aerosol. The new instrument combines proton-transfer-reaction mass-spectrometry (PTR-MS) with a collection-thermal-desorption aerosol sampling technique. For secondary organic aerosol produced from the reaction of ozone with isoprenoids in a laboratory reactor, the TD-PTR-MS instrument detected typically 80% of the mass that was measured with a scanning mobility particle sizer (SMPS). The first field deployment of the instrument was the EUCAARI-IOP campaign at the CESAR tall tower site in the Netherlands. For masses with low background values (similar to 30% of all masses) the detection limit of aerosol compounds was below 0.2 ng/m(3) which corresponds to a sampled compound mass of 35 pg. Comparison of thermograms from ambient samples and from chamber-derived secondary organic aerosol shows that, in general, organic compounds from ambient aerosol samples desorb at much higher temperatures than chamber samples. This suggests that chamber aerosol is not a good surrogate for ambient aerosol and therefore caution is advised when extrapolating results from chamber experiments to ambient conditions.
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页码:2257 / 2267
页数:11
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