Vibrational Distribution Functions in Anharmonic Oscillators
- 15 July 1971
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 55 (2) , 552-561
- https://doi.org/10.1063/1.1675787
Abstract
A model has been developed to calculate the steady‐state vibrational distribution of an anharmonic oscillator under conditions of thermal nonequilibrium. The model includes vibration–vibration and vibration–translation collisional processes as well as radiative decay. Numerical calculations are shown to be in reasonably good agreement with experimental data obtained in electrically excited N2–CO mixing systems. It is shown that radiative decay may be the dominant loss mechanism in low‐pressure N2–CO experiments.Keywords
This publication has 13 references indexed in Scilit:
- Vibrational relaxation rates for CO(ν ⩽ 13) with CO(ν = 0), OCS, O2 and HeChemical Physics Letters, 1971
- Vibrational distribution of populations and kinetics of the CO–N2 system in the fundamental and harmonic regionsCanadian Journal of Physics, 1970
- Mechanism of a CO–N2 laser. I. Study of the vibrational populationsCanadian Journal of Physics, 1970
- Nonequilibrium Vibrational Distribution Functions in Infrared Active Anharmonic OscillatorsThe Journal of Chemical Physics, 1970
- Energy Transfer in Near-Resonant Molecular Collisions due to Long-Range Forces with Application to Transfer of Vibrational Energy from ν3 Mode of CO2 to N2The Journal of Chemical Physics, 1969
- Vibrational relaxation of anharmonic oscillator molecules: Relaxation under isothermal conditionsJournal of Physics B: Atomic and Molecular Physics, 1968
- Vibrational Relaxation of Anharmonic Oscillators with Exchange-Dominated CollisionsThe Journal of Chemical Physics, 1968
- First- and Second-Overtone Intensity Measurements for CO and NOThe Journal of Chemical Physics, 1966
- Interchange of Vibrational Energy between Molecules in CollisionsThe Journal of Chemical Physics, 1965
- Calculation of Vibrational Relaxation Times in GasesThe Journal of Chemical Physics, 1952