Modified Pd catalysts for the selective hydrogenation of acetylene

被引:116
|
作者
Kim, Woo-Jae [2 ]
Moon, Sang Heup [1 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151744, South Korea
[2] Kyungwon Univ, Div Energy & Biol Engn, Songnam 461701, Gyeonggi Do, South Korea
关键词
Acetylene hydrogenation; Si; SMSI; Cu; Selective deposition; Structure sensitivity; METAL-SUPPORT INTERACTIONS; ETHYLENE HYDROGENATION; DEACTIVATION BEHAVIOR; PALLADIUM CATALYSTS; PD/SIO2; CATALYSTS; MULTIPLE BONDS; PARTICLE-SIZE; SURFACE; PERFORMANCE; CARBON;
D O I
10.1016/j.cattod.2011.09.037
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This article reviews our previous studies to develop high performance catalysts for acetylene hydrogenation. Ethylene selectivity of Pd catalysts in acetylene hydrogenation was improved by adding Si, metal oxides showing SMSI behavior, and either Ag or Cu as promoters. The promoter effect was further enhanced by maximizing the interactions between Pd and added promoters. Chemical vapor deposition was used for the addition of Si, high-temperature reduction for the SMSI metal oxides, and a surface redox (SR) for Ag and Cu. Si modified the Pd surface geometrically, SMSI metal oxides modified Pd both electronically and geometrically, and Ag modified Pd largely electronically. Cu added by SR modified Pd electronically to a small extent, but preferentially decorated the low-coordination sites of Pd such that the ethylene selectivity of the optimum catalyst was significantly promoted from that of Pd, while its activity remained comparable to that of Pd. The sensitivity of ethylene selectivity to the surface structure of Pd was demonstrated using model catalysts containing uniform-sized Pd particles in either cubic or spherical shapes. The three stage deactivation of the Pd catalyst and the self-regenerative behavior in early stages of deactivation were also investigated. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2 / 16
页数:15
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