C-13 HIGH-RESOLUTION NMR-STUDIES OF ADSORPTION AND REACTION OF ETHYLENE ON SILICA-SUPPORTED RU AND RU-CU CATALYSTS

被引:5
|
作者
PRUSKI, M
KELZENBERG, JC
SPROCK, M
GERSTEIN, BC
KING, TS
机构
[1] IOWA STATE UNIV SCI & TECHNOL,DEPT CHEM ENGN,AMES,IA 50011
[2] IOWA STATE UNIV SCI & TECHNOL,DEPT CHEM,AMES,IA 50011
来源
COLLOIDS AND SURFACES | 1990年 / 45卷
关键词
D O I
10.1016/0166-6622(90)80013-T
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
The adsorption and subsequent reaction of ethylene on silica-supported Ru and RuCu bimetallic catalysts have been studied via nuclear magnetic resonance (NMR) employing a variety of experimental nuclear spin dynamics. NMR of 13C using cross polarization (CP) and magic angle spinning (MAS) allowed us to simultaneously observe transformations of chemisorbed species and weakly adsorbed molecules. Direct 13C excitation allowed quantitative measurements of various species on the surface. At room temperature the ethylene adsorbed on the ruthenium catalysts rapidly and converted to strongly adsorbed acetylide and alkyl species. Weakly adsorbed ethane, butane and cis- and trans-2-butene were observed. The butene slowly hydrogenated to form additional butane. When the temperature was raised to 140°C propane and methane were observed suggesting hydrogenolysis of the product molecules. The introduction of copper into the catalysts reduced the hydrogenation capability while still maintaining the ability to form dimeric products. In addition to butene and butane, butadiene was observed on the bimetallic catalysts. © 1990.
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页码:39 / 56
页数:18
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