## Abstract The rate of vibrational relaxation of HF(__v__ = 1) by F atoms has been calculated using quasiβclassical trajectory techniques. An attempt has been made to account for the effects of multiple potential energy surfaces on the vibrational relaxation efficiency within the electronically ad
Deactivation of HF(v =1) by F, O, and H atoms
β Scribed by G.P. Quigley; G.J. Wolga
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 389 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The laser induced fluorescence method has been used to measure the rate of deactivation of HF(u = 1) by F, 0, and H atoms at 300Β°K. The rate for F-atoms was found to be kF_HF = (0.9 f 0.2) X lo4 set-' torr-', for Oatoms Lo_m = (1.0 f 0.2) X lo5 set-' torr-', and for Hatoms, an upper limit to the rate was found to be k&m < 0.5 X lo3 set-' torr-' . The results are explained qualitatively in terms of a vibronic to translational energy transfer mechanism.
π SIMILAR VOLUMES
## Abstract Measurements have been made which provide information concerning the rate of energy transfer between vibrationally excited HF and atomic fluorine. It was found that HF (__v__ = 1) deactivates about seven times slower than was determined in previous experiments. The deactivation rate con
VibrationaII of mixtures of $6 excited 160190(3~~) has been observed at short delay times during the flash photoIysia 03 and 1602. This s !Y an 1802 molecule, indicating that 02( ties can only be formed by the reaction of an 160(lD) atom with C &R,O ia a product of the collisiocaI deactivation of O(
Rate constants have been determined at (298 \* 4) K for the reactions: and the relaxation processes: (lb) HF(u = 1) + HCN -HF(v = 0) + HCN Time-resolved HF(1,O) emission was observed following the photolysis of Fz with pulses from an excimer laser operating on XeCl ( h = 308 nm). Analysis of the