Transition State Theory of Zeolitic Diffusion: Diffusion of CH4 and CF4 in 5A Zeolite

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DC Field	Value	Language
dc.contributor.author	Ruthven, D. M.	-
dc.contributor.author	Derrah, R. I.	-
dc.date.accessioned	2025-02-03T13:20:08Z	-
dc.date.available	2025-02-03T13:20:08Z	-
dc.date.issued	1972	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/17140	-
dc.description.abstract	A simple theory of zeolitic diffusion is developed from the principles of transition state theory. General expressions for the diffusivity are derived in terms of the lattice parameter and the partition function for the transition state which, for the type A zeolites, is identified as a molecule in passage through the 8-membercd oxygen window. Theoretical diffusivities calculated for CH4 and CF4 in 5A zeolite agree well with experimental data and it is shown that, in the transition state, the CF4 molecule has a high degree of rotational freedom whereas the rotation of the CH4 molecule is severely restricted. This difference is attributed to the difference in the moments of inertia.	en_US
dc.language.iso	en	en_US
dc.publisher	Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1972, 68 (12)	en_US
dc.subject	Chemistry	en_US
dc.subject	Zeolitic Diffusion	en_US
dc.subject	Transition State Theory	en_US
dc.subject	Journal of the Chemical Society : Faraday Transaction - I	en_US
dc.title	Transition State Theory of Zeolitic Diffusion: Diffusion of CH4 and CF4 in 5A Zeolite	en_US
dc.type	Article	en_US
Appears in Collections:	Journal Articles (before-1995)

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