gamma-Al2O3-supported Re-Pt cluster catalyst prepared from [Re2Pt(CO)(12)]: Characterization by extended X-ray absorption fine structure spectroscopy and catalysis of methylcyclohexane dehydrogenation

被引:64
作者
Fung, AS
Kelley, MJ
Koningsberger, DC
Gates, BC
机构
[1] UNIV UTRECHT,INORGAN CHEM & CATALYSIS LAB,DEBYE INST,NL-3508 TB UTRECHT,NETHERLANDS
[2] UNIV DELAWARE,DEPT CHEM ENGN,CTR CATALYT SCI & TECHNOL,NEWARK,DE 19716
[3] DUPONT CO INC,WILMINGTON,DE 19898
[4] UNIV CALIF DAVIS,DEPT CHEM ENGN & MAT SCI,DAVIS,CA 95616
关键词
D O I
10.1021/ja962816z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A model catalyst prepared from [Re2Pt(CO)(12)] supported on gamma-Al2O3 was characterized by extended X-ray absorption fine structure (EXAFS) spectroscopy, and its stability in operation in a flow reactor was tested for the dehydrogenation of methylcyclohexane at 1 atm and 400 degrees C. EXAFS data characterizing the unused catalyst measured at both the Re L-III and Pt L-III edges at liquid nitrogen temperature with the sample in the presence of H-2 distinguish the Re-Pt from the Pt-Pt and Re-Re interactions. The EXAFS results form the basis of a simplified model of the supported bimetallic structures, consisting of Re4Pt2 entities, with oxophilic Re in a low positive oxidation state interacting strongly with the oxygen atoms of the gamma-Al2O3 support and stabilizing the dispersion of the Pt atoms. The catalyst made from [Re2Pt(CO)(12)] was found to be more resistant to deactivation during catalytic dehydrogenation of methylcyclohexane than catalysts prepared conventionally from Re and Pt salt precursors. The catalyst prepared from [Re2Pt(CO)(12)] was more highly dispersed than the others, and its resistance to deactivation is attributed to the role of Re in stabilizing the dispersion of the Pt.
引用
收藏
页码:5877 / 5887
页数:11
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