Vibrational deactivation of O3 molecules in gas mixtures. II.
- 15 January 1975
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 62 (2), 466-476
- https://doi.org/10.1063/1.430500
Abstract
Experimental measurements of the rate constants for vibrational deactivation of O3 by O3, O2, CO2, H2, D2, CH4, N2, He, Ar, SF6, CH3Cl, CH2Cl2, CCl4, and C2H2 are presented. Vibrational relaxation of O3 is shown to follow the sequence (1) rapid V → V intermode coupling between the ν1 and ν3 modes, (2) a slower coupling of the ν1, ν3 modes to the ν2 mode, and (3) V → T relaxation through the O3(010) level. The results are described in terms of a simple analytic model for vibrational relaxation of O3.Keywords
This publication has 13 references indexed in Scilit:
- The reaction of nitric oxide with vibrationally excited ozoneChemical Physics Letters, 1973
- On the interpretation of vibrational relaxation measurementsChemical Physics Letters, 1973
- Infrared double resonance in boron trichlorideThe Journal of Chemical Physics, 1973
- Deactivation of laser excited CH3F in CH3F–X mixturesThe Journal of Chemical Physics, 1973
- Laser Induced Infrared Fluorescence: Thermal Heating, Mass Diffusion, and Collisional Relaxation in SF6The Journal of Chemical Physics, 1972
- Temperature Dependence of Nearly Resonant Vibration → Vibration Energy Transfer in CO2 MixturesThe Journal of Chemical Physics, 1972
- Vibrational Relaxation of Anharmonic Oscillators with Exchange-Dominated CollisionsThe Journal of Chemical Physics, 1968
- Relaxation of a Gas of Harmonic OscillatorsThe Journal of Chemical Physics, 1967
- Relaxation of an Isolated Ensemble of Harmonic OscillatorsThe Journal of Chemical Physics, 1960
- Calculation of Vibrational Relaxation Times in GasesThe Journal of Chemical Physics, 1952