Vibrational Relaxation of Methane by Oxygen Collisions: Measurements of the Near-Resonant Energy Transfer between CH4 and O2 at Low Temperature

Abstract

Vibrational relaxation in methane-oxygen mixtures has been investigated by means of a time-resolved pump-probe technique. Methane molecules are excited into selected rotational levels by tuning the pump laser to 2nu3 lines. The time evolution in population of various vibrational levels after the pumping pulse is monitored by probing, near 3000 cm-1, stretching transitions between various polyads like 2nu3(F2) - nu3, (nu3+2nu4) - 2nu4, and (nu3+nu4) - nu4 transitions. Measurements were performed from room temperature down to 190 K. A numerical kinetic model, taking into account the main collisional processes connecting energy levels up to 6000 cm(-1), has been developed to describe the vibrational relaxation. The model allows us to reproduce the observed signals and to determine rate coefficients of relaxation processes occurring upon CH4-O2 collisions. For the vibrational energy exchange, the rate coefficient of transfer from O2 (v = 1) to CH4 is found equal to (1.32 +/- 0.09) x 10(-12) cm3 molecule-1 s(-1) at 296 K and to (1.50 +/- 0.08) x 10(-12) cm3 molecule(-1) s(-1) at 193 K.