Vibrational deactivation of O3 molecules in gas mixtures. II.
David I. Rosen, Terrill A. Cool
Abstract
David I. Rosen, Terrill A. Cool
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.
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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.
Key concepts: Vibrational energy relaxation, Relaxation (psychology), Chemistry, Molecular vibration, Molecule, Atomic physics, Coupling (piping), Molecular physics