Selective detection of isomers with photoionization mass spectrometry for studies of hydrocarbon flame chemistry

被引:268
作者
Cool, TA [1 ]
Nakajima, K
Mostefaoui, TA
Qi, F
McIlroy, A
Westmoreland, PR
Law, ME
Poisson, L
Peterka, DS
Ahmed, M
机构
[1] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14886 USA
[2] Sandia Natl Labs, Combust Res Facil, Livermore, CA 94551 USA
[3] Univ Massachusetts, Dept Chem Engn, Amherst, MA 01003 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA
关键词
D O I
10.1063/1.1611173
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the first use of synchrotron radiation, continuously tunable from 8 to 15 eV, for flame-sampling photoionization mass spectrometry (PIMS). Synchrotron radiation offers important advantages over the use of pulsed vacuum ultraviolet lasers for PIMS; these include superior signal-to-noise, soft ionization, and access to photon energies outside the limited tuning ranges of current VUV laser sources. Near-threshold photoionization efficiency measurements were used to determine the absolute concentrations of the allene and propyne isomers of C3H4 in low-pressure laminar ethylene-oxygen and benzene-oxygen flames. Similar measurements of the isomeric composition of C2H4O species in a fuel-rich ethylene-oxygen flame revealed the presence of substantial concentrations of ethenol (vinyl alcohol) and acetaldehyde. Ethenol has not been previously detected in hydrocarbon flames. Absolute photoionization cross sections were measured for ethylene, allene, propyne, and acetaldehyde, using propene as a calibration standard. PIE curves are presented for several additional reaction intermediates prominent in hydrocarbon flames. (C) 2003 American Institute of Physics.
引用
收藏
页码:8356 / 8365
页数:10
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