Arrhenius parameters of the reaction CH3·+ C2H6→ CH4+ C2H5·
- 1 January 1972
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases
- Vol. 68, 1462-1473
- https://doi.org/10.1039/f19726801462
Abstract
Study of ethane pyrolysis over the ranges 920–1040 K and 0–200 Torr in a flow system allows evaluation of Arrhenius parameters for the reactions C2H6→ 2CH3·(1), CH3·+ C2H6→ CH4+ C2H5·(2) The results obtained are, log(A1/s–1)= 16.7, E1= 370 kJ mol–1, in close agreement with recent measurements, and log(A2/l. mol–1 s–1)= 11.7 ± 1.0, E2= 90 ± 20 kJ mol–1. The latter values conflict with estimates based on low temperature studies but are consistent with pyrolytic estimates for comparable reactions. It is shown that all available data for k2 fall on a common curve indicating that the relevant Arrhenius parameters are strongly temperature dependent. The origin of this behaviour is briefly discussed and its probable generality for metathetical reactions of alkyl radicals is indicated. Discrepancies in the balance of methane and n-butane yields are shown to be explicable on the grounds of the occurrence of the minor, primary reaction H + C2H5·→ 2CH3·(7) which proceeds at a rate comparable with chain termination processes.Keywords
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