Vibrational relaxation and vibration-rotation energy transfer between highly vibrationally excited KH(X1Σ+, v=14–21) and CO2

2012 ◽  
Vol 113 (16) ◽  
pp. 2081-2087 ◽  
Author(s):  
Xiu-hua Cui ◽  
Bao-xia Mu ◽  
Yi-fan Shen ◽  
Kang Dai
1974 ◽  
Vol 52 (10) ◽  
pp. 854-860 ◽  
Author(s):  
W. G. Tam

A semiclassical theory of the vibration–rotation energy transfer of fast rotating molecules is presented. The formulation is based on the same model as that of Shin's classical theory. The semiclassical theory is simpler to derive and more rigorous. We show that it necessarily gives more accurate results than the classical theory. Applications to the systems HF and DF indicate that the two theories agree reasonably well in these cases.


1992 ◽  
Vol 97 (5) ◽  
pp. 3348-3356 ◽  
Author(s):  
Adolf Miklavc ◽  
Nikola Marković ◽  
Gunnar Nyman ◽  
Vili Harb ◽  
Sture Nordholm

1988 ◽  
Vol 88 (2) ◽  
pp. 1460-1461 ◽  
Author(s):  
Francis W. Farley ◽  
Leo V. Novakoski ◽  
Manvendra K. Dubey ◽  
Gilbert M. Nathanson ◽  
Gary M. McClelland

The absolute efficiencies for the vibrational excitation of molecules which quench singlet molecular oxygen have been determined from measurements of their infrared chemiluminescence and kinetics of relaxation. The systems studied were NO and CO with O 2 ( 1 ∆ g ) and NO, CO, HCl, DCl, H 2 O, D 2 O, CO 2 , N 2 O, NH 3 and C 2 H 2 with O 2 ( 1 ∑ + g ). Rate coefficients for the vibrational relaxation of a number of these molecules by molecular oxygen were also determined.


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