Ben Bouchrit R, Jorfi M, Ben Abdallah D, Jaidane N, González M, Bussery-Honvault B, Honvault P
Laboratoire de Physique Atomique et Moléculaire et Applications, Département de Physique, Faculté des Sciences, Université Tunis-El Manar, 1060 Tunis, Tunisia.
Institut de Chimie des Milieux et des Matériaux de Poitiers, UMR CNRS 6503, Université de Poitiers, 86022 Poitiers Cedex, France.
J Chem Phys. 2014 Jun 28;140(24):244315. doi: 10.1063/1.4885276.
Time independent quantum mechanical (TIQM) scattering calculations have been carried out for the O((1)D) + CH4(X(1)A1) → CH3(X(2)A2″) + OH(X(2)Π) atmospheric reaction, using an ab initio ground potential energy surface where the CH3 group is described as a pseudo-atom. Total and state-to-state reaction probabilities for a total angular momentum J = 0 have been determined for collision energies up to 0.5 eV. The vibrational and rotational state OH product distributions show no specific behavior. The rate coefficient has been calculated by means of the J-shifting approach in the 10-500 K temperature range and slightly depends on T at ordinary temperatures (as expected for a barrierless reaction). Quantum effects do not influence the vibrational populations and rate coefficient in an important way, and a rather good agreement has been found between the TIQM results and the quasiclassical trajectory and experimental ones. This reinforces somewhat the reliability of the pseudo-triatomic approach under the reaction conditions explored.
