Vibrational relaxation of NO X 2Π(v = 1) in the temperature range 100–300 °K
- 1 June 1974
- journal article
- research article
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 60 (11), 4289-4294
- https://doi.org/10.1063/1.1680902
Abstract
Laser‐excited fluorescence measurements have given rate constants for the vibrational deactivation of NO(v=1) by NO, He, and N2, and for the V–V exchange between CO(v=1) and NO(v=1) in the temperature region 100–300°K. Relaxation was caused entirely by bimolecular collisions. Deactivation rates of NO(v=1) by H2O, D2O, NO2, CH4, C2H4, C2H6, and C4H10, and of N2(v=1) by NO and CO(v=1) by NO2 and N2O4 were measured at T=298°K.Keywords
This publication has 17 references indexed in Scilit:
- Temperature dependence of vibrational relaxation in the HF, DF, HF–CO2, and DF–CO2 systemsThe Journal of Chemical Physics, 1974
- Vibrational relaxation of HF in the temperature range 600–2400 °KThe Journal of Chemical Physics, 1973
- Vibrational excitation and relaxation of the CO(v=1) and CO(v=2) statesApplied Physics Letters, 1973
- Vibrational relaxation of HF and DFThe Journal of Chemical Physics, 1973
- Shock tube study of DF vibrational relaxationThe Journal of Chemical Physics, 1973
- Temperature Dependence of Nearly Resonant Vibration → Vibration Energy Transfer in CO2 MixturesThe Journal of Chemical Physics, 1972
- Vibration-rotation-translation energy transfer in HF-HF and DF-DFChemical Physics Letters, 1971
- Kinetics and mechanism of the vibrational relaxation of NOX2Π(v= 1) in the temperature range 100–433 KTransactions of the Faraday Society, 1971
- Laser studies of vibrational energy transferAccounts of Chemical Research, 1969
- Absolute infrared intensity measurements on the fundamental of NOJournal of Quantitative Spectroscopy and Radiative Transfer, 1967