Chemical relaxation in a radiation field

Chemical relaxation in a radiation field

Publication Type:

Journal Article

Authors:

Kapral, R.

Source:

The Journal of Chemical Physics, Volume 61, Number 5, p.1723-1729 (1974)

URL:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-0348192151&doi=10.1063%2f1.1682168&partnerID=40&md5=5d6a90b4a140653e66af363006b5bea7

Abstract:

The relaxation processes occurring in a chemically reacting gas irradiated by a monochromatic light source are investigated. For the case of a bimolecular isomerization, the decay of the progress variable of the reaction to the steady state produced by the illumination is studied. A macroscopic equation-for this quantity is derived from the quantum mechanical Boltzmann equation for this system by projection operator methods. The derivation also provides microscopic expressions for the rate coefficients which depend on time (or frequency). The rate coefficients which characterize the one way fluxes in the steady state are compared with the observed rate coefficients. Calculations for specific models of the isomerization indicate that significant differences between these quantities occur at all values of the light intensity. In addition, the time evolution of the part of the rate coefficient which depends on the coupling between the chemical and internal relaxation processes is studied and compared with the decay of the progress variable. Copyright © 1974 American Institute of Physics.