Abstract
Self- and helium-broadened carbon monoxide linewidths have been inverted to obtain state-to-state rate constants using the energy corrected sudden scaling formalism. Selected rotation-rotation and rotation-translation rate constants are discussed as a function of vibrational and rotational levels for the CO-CO and He-CO systems. We find that there is no dependence of the collision dynamics upon the vibrational state of the collision partners up to υ=3. In addition, relaxation in both these systems is found to be dominated by rotation-translation collisions. However they are qualitatively different in their dynamical characteristics and result in signficantly varied state-to-state rate constants. An analysis of the effect of collision partners in the CO-X (X=CO, He, Ne, Ar, Xe, H2) system is presented. Comparisons are made with the available data in the literature.
Original language | English (US) |
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Pages (from-to) | 3990-3998 |
Number of pages | 9 |
Journal | The Journal of chemical physics |
Volume | 78 |
Issue number | 6 |
DOIs | |
State | Published - 1983 |
All Science Journal Classification (ASJC) codes
- General Physics and Astronomy
- Physical and Theoretical Chemistry