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Dehydrogenation and isomerization of n-butenes on mixed tin + antimony oxide catalysts

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dc.contributor.author Irvine, Elizabeth A.
dc.contributor.author Taylor, Duncan
dc.date.accessioned 2025-04-24T09:40:08Z
dc.date.available 2025-04-24T09:40:08Z
dc.date.issued 1978
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18769
dc.description.abstract The dehydrogenation and concurrent isomerization of the three n-butenes have been investigated at 474 K on a range of mixed tin + antimony oxide catalysts outgassed at 698 K. The initial approximately zero order reaction rates were used as a measure of catalytic activity to construct patterns of activity as a function of catalyst composition. Comparison of the patterns with those for the isomerization of 3,3-dimethylbut-1-ene and for the selective oxidation of propene on the same catalysts indicate that dehydrogenation of but-1-ene involves a π-allyl intermediate, while isomerization occurs through carbonium ion formation. For the cis- and trans-isomers, it is suggested that both reactions occur via a common allyl (but not π-allyl) type of intermediate. en_US
dc.language.iso en en_US
dc.publisher Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (06) en_US
dc.subject Chemistry en_US
dc.subject Dehydrogenation of n-butenes en_US
dc.subject Isomerization of n-butenes en_US
dc.subject Journal of the Chemical Society : Faraday Transaction - I en_US
dc.title Dehydrogenation and isomerization of n-butenes on mixed tin + antimony oxide catalysts en_US
dc.type Article en_US


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