Acetylene hydrogenation over structured Au-Pd catalysts

被引:36
作者
McCue, Alan J. [1 ]
Baker, Richard T. [2 ]
Anderson, James A. [1 ]
机构
[1] Univ Aberdeen, Sch Engn, Surface Chem & Catalysis Grp, Mat & Chem Engn, Aberdeen AB24 3UE, Scotland
[2] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
关键词
GALLIUM INTERMETALLIC COMPOUNDS; GOLD-PALLADIUM NANOPARTICLES; ETHENE-RICH STREAMS; SELECTIVE HYDROGENATION; ALKYNE HYDROGENATION; SILVER NANOPARTICLES; CU/AL2O3; CATALYSTS; SUBSURFACE CARBON; MODIFIED PD/TIO2; SHELL THICKNESS;
D O I
10.1039/c5fd00188a
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
AuPd nanoparticles were prepared following a methodology designed to produce coreshell structures ( an Au core and a Pd shell). Characterisation suggested that slow addition of the shell metal favoured deposition onto the pre-formed core, whereas more rapid addition favoured the formation of a monometallic Pd phase in addition to some nanoparticles with the core-shell morphology. When used for the selective hydrogenation of acetylene, samples that possessed monometallic Pd particles favoured over-hydrogenation to form ethane. A sample prepared by the slow addition of a small amount of Pd resulted in the formation of a core-shell structure but with an incomplete Pd shell layer. This material exhibited a completely different product selectivity with ethylene and oligomers forming as the major products as opposed to ethane. The improved performance was thought to be as a result of the absence of Pd particles, which are capable of forming a Pd-hydride phase, with enhanced oligomer selectivity associated with reaction on uncovered Au atoms.
引用
收藏
页码:499 / 523
页数:25
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