We report a direct Monte Carlo simulation of a Lindemann-Christiansen unimolecular reaction system. The simulation is carried out at the molecular level and includes energy transfer among reactants and products as well as the reaction steps. The usual differential equations of chemical kinetics are
A New Formulation of the Lindemann Mechanism of Unimolecular Reactions
β Scribed by Ren-Yuan Qian
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 275 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0256-7660
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β¦ Synopsis
Abstract
A new formulation of the Lindemann mechanism of unimolecular reactions in gaseous phase is presented, without the use of steady state hypothesis. It is hereby shown that the nature of applicability of steady state hypothesis in the regime of high reactant gas pressure is different from that in the regime of low gas pressure. In the former case it is an equilibrium approximation, while in the latter case it is a highly reactive intermediate approximation in no connection with a steady state. Furthermore for the latter case it is shown that in the classical formulation of Lindemann mechanism the use of steady state hypothesis is an ad hoc assumption. A highly reactive intermediate in the sense that its concentration is very small during the whole course of reaction is a necessary condition for the applicability of very reactive intermediate approximation. When the two distinctive nature of the applicability of steady state hypothesis is mixedβup, wrong or useless conclusion may be arrived at. The only possible case of realizing a true steady state in a complex reaction is pointed out.
π SIMILAR VOLUMES
## Abstract The Lindemann mechanism explains how apparent unimolecular chemical reactions arise from bimolecular collisions. In this mechanism an ingredient M activates reactants A through collisions, and the resulting activated species A\* can either decay to products P or be deactivated back to A