An experimental and theoretical high temperature kinetic study of the thermal unimolecular dissociation of fluoroethane

被引:10
作者
Giri, Binod R. [1 ]
Kiefer, John H. [2 ]
Xu, Hui [2 ]
Klippenstein, Stephen J. [1 ]
Tranter, Robert S. [1 ]
机构
[1] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
[2] Univ Illinois, Dept Chem Engn, Chicago, IL 60607 USA
关键词
D O I
10.1039/b808168a
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
The thermal dissociation of fluoroethane has been studied using shock tube (ST)/time-of-flight mass spectrometry (TOF-MS) at 500 and 1200 Torr over the temperature range 1200-1550 K. The ST/TOF-MS experiments confirm that elimination of HF is the only reaction channel and rate coefficients for this reaction were extracted from concentration/time profiles derived from the mass spectra. Results from a novel diaphragmless shock tube coupled to the TOF-MS are also presented and demonstrate the unique ability of this apparatus to generate sufficiently reproducible shock waves that signal averaging can be performed over multiple experiments; something that is not possible with a conventional shock tube. The dissociation is also studied with ab initio transition state theory based master equation simulations. A modest increase in the calculated barrier height (i.e., by 1 kcal mol(-1)) yields predicted high pressure rate coefficients that are in good agreement with the existing literature data. The present pressure dependent observations are accurately reproduced for a downwards energy transfer for neon at 1200 to 1500 K of similar to 270 cm(-1), which is somewhat smaller than that found in previous studies on fluorinated ethanes with the same bath gases.
引用
收藏
页码:6266 / 6273
页数:8
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