Probabilities of vibrational energy exchange between carbon dioxide and carbon tetrafluoride

1984 ◽  
Vol 81 (2) ◽  
pp. 738-741 ◽  
Author(s):  
Carlos Manzanares I ◽  
Emilio Colón
1983 ◽  
Vol 79 (7) ◽  
pp. 3596-3597 ◽  
Author(s):  
Jeffrey Hoke ◽  
J. M. Preses ◽  
Ralph E. Weston

1997 ◽  
Author(s):  
John Gilmore ◽  
Surendra Sharma ◽  
Deepak Bose ◽  
Graham Candler ◽  
John Gilmore ◽  
...  

1993 ◽  
Vol 71 (3-4) ◽  
pp. 142-146 ◽  
Author(s):  
L. Wang ◽  
J. R. Xu ◽  
W. E. Jones

The CARS (coherent anti-Stokes Raman scattering) technique has been used for the first time to observe directly the vibrational energy transfer between nitrogen N2 (X1Σ, ν = 1, 2) and carbon dioxide. The transfer-rate constants were determined as (1.0 ± 0.1) × 1011 cm3 mol−1 s−1 and (1.7 ± 0.4) × 1011 cm3 mol−1 s−1 for N2(ν = 1) and N2(ν = 2), respectively.


2008 ◽  
Vol 113 (G2) ◽  
pp. n/a-n/a ◽  
Author(s):  
Christian Brümmer ◽  
Ulrike Falk ◽  
Hans Papen ◽  
Jörg Szarzynski ◽  
Reiner Wassmann ◽  
...  

1972 ◽  
Vol 50 (9) ◽  
pp. 889-897 ◽  
Author(s):  
P. H. Dawson ◽  
W. G. Tam

The role of V–V processes in vibrationally excited CO systems in the longitudinal and transverse flow chemical lasers is studied. Initial vibrational energy distributions of CO formed by the O + CS reaction are deduced from chemiluminescent data using calculated values of the vibration energy exchange probabilities. The time evolution of the population distributions is then obtained by computer simulation. The results are compared with experimental measurements. The effects of excess oxygen and of "cold" CO on the population distributions are also discussed.


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