Pressure and temperature dependence of dissociative and non-dissociative electron attachment to CF3: Experiments and kinetic modeling

被引:32
|
作者
Shuman, Nicholas S. [2 ]
Miller, Thomas M. [2 ]
Friedman, Jeffrey F. [2 ]
Viggiano, Albert A. [2 ]
Maergoiz, Anatol I. [1 ]
Troe, Juergen [1 ,3 ]
机构
[1] Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany
[2] USAF, Res Lab, Space Vehicles Directorate, Kirtland AFB, NM 87117 USA
[3] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 2011年 / 135卷 / 05期
关键词
carbon compounds; dissociation; electron attachment; mass spectra; molecule-electron collisions; statistical analysis; RATE CONSTANTS K(E; J); UNIMOLECULAR REACTIONS; CROSS-SECTIONS; CAPTURE; IONS;
D O I
10.1063/1.3614471
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 kinetics of electron attachment to CF3 as a function of temperature (300-600 K) and pressure (0.75-2.5 Torr) were studied by variable electron and neutral density attachment mass spectrometry exploiting dissociative electron attachment to CF3Br as a radical source. Attachment occurs through competing dissociative (CF3 + e(-) -> CF2 + F-) and non-dissociative channels (CF3 + e(-) -> CF3-). The rate constant of the dissociative channel increases strongly with temperature, while that of the non-dissociative channel decreases. The rate constant of the non-dissociative channel increases strongly with pressure, while that of the dissociative channel shows little dependence. The total rate constant of electron attachment increases with temperature and with pressure. The system is analyzed by kinetic modeling in terms of statistical theory in order to understand its properties and to extrapolate to conditions beyond those accessible in the experiment. (C) 2011 American Institute of Physics. [doi:10.1063/1.3614471]
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页数:10
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