SELECTIVE HYDROGENATION OF CINNAMALDEHYDE CONTROLLED BY HOST-GUEST INTERACTIONS IN BETA-ZEOLITE

被引:0
|
作者
GALLEZOT, P [1 ]
BLANC, B [1 ]
BARTHOMEUF, D [1 ]
DASILVA, MIP [1 ]
机构
[1] UNIV PARIS 06,REACT SURFACE LAB,F-75252 PARIS 5,FRANCE
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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
Large Pt-particles encapsulated in beta zeolite were obtained by direct H-2-reduction of Pt-exchanged zeolite beta. This catalyst gives a high selectivity to unsaturated alcohol in cinnamaldehyde hydrogenation because the geometric constraints in micropores impose an adsorption of the molecule via the C=O group. When the zeolite is calcinated in O-2 before reduction, Pt-clusters of size less than or equal to 1nm are obtained in the micropores. A simultaneous hydrogenation of the C=C and C=O bonds occurs initially on the smaller clusters but the selectivity to unsaturated alcohol increases with time probably as a result of a coalescence of the smaller clusters into clusters filling the open space in the micropores.
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页码:1433 / 1439
页数:7
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