Regioselective hydrogenation of alkenes over Pt-loaded zeolite BEA

被引:8
作者
Creyghton, EJ
Grotenbreg, RAW
Downing, RS
vanBekkum, H
机构
[1] Laboratory of Organic Chemistry and Catalysis, Delft University of Technology, 2628 BL Delft
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1996年 / 92卷 / 05期
关键词
D O I
10.1039/ft9969200871
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:871 / 877
页数:7
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