Long-Time Stability vs Deactivation of Pd-Ag/Al2O3 Egg-Shell Catalysts in Selective Hydrogenation of Acetylene

被引:74
作者
Kuhn, Martin [1 ]
Lucas, Martin [1 ]
Claus, Peter [1 ]
机构
[1] Tech Univ Darmstadt, Dept Chem, Ernst Berl Inst, Chem Technol 2, D-64287 Darmstadt, Germany
关键词
SUPPORTED METAL-CATALYSTS; GALLIUM INTERMETALLIC COMPOUNDS; PALLADIUM PARTICLE-SIZE; CARBON-MONOXIDE; PD; ETHYLENE; AG; PERFORMANCE; ALUMINA; COKE;
D O I
10.1021/acs.iecr.5b01682
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Industrial relevant Pd-Ag/Al2O3 egg-shell catalysts with varying Pd/Ag mole ratios were prepared, characterized (CO chemisorption, DRIFTS, EPMA, STEM, coupled with Ens and EDX, as well as TPR) and tested for selective hydrogenation of acetylene under tail-end conditions. Characterization suggests a reduction of the total number of Pd surface atoms n(Pd,surf) as well as an isolation of large Pd ensembles. The effect of silver addition on byproduct formation and deactivation behavior was investigated, representing a higher long time stability of Pd-5-Ag-95/Al2O3 in comparison to silver free Pd-100/Al2O3 egg-shell catalysts, due to a decrease of green oil and coke formation. The selectivity to C-6 compounds is a fundamental indicator for long-term stability of palladium catalysts that is often overlooked in the literature. Furthermore, this study implicates selective hydrogenation of acetylene as a structure sensitive reaction originating from a geometric effect.
引用
收藏
页码:6683 / 6691
页数:9
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