
Journal of the Chemical Society - Faraday Transactions p. 871 - 877 (1996)
Update date:2022-08-11
Topics:
Creyghton, Edward J.
Grotenbreg, Robert A. W.
Downing, Roger S.
Van Bekkum, Herman
The hydrogenation of dec-1-ene and of (E)-dec-5-ene has been studied over platinum/Na-BEA and non-zeolitic platinum catalysts. Provided that the solvent does not compete with the substrates for sorption in the zeolite, and that the external surface platinum is deactivated with a bulky phosphine, dec-1-ene is hydrogenated 18 times faster than (E)-dec-5-ene, whereas the ratio is only ca. 2 for platinum on non-microporous supports. This regioselectivity is explained by steric constraints imposed by the microporous structure of the zeolite. The hydrogenation rate over platinum/Na-BEA is much lower than that observed over the amorphous supported platinum catalysts; further, for the zeolite-based catalyst, approximately first-order kinetics are found compared with zero-order for the amorphous catalysts. Both effects can be explained in terms of alkene coverage of the Pt sites in the two types of catalyst.
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