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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:74
|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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