Characterisation and activity evaluation of silica supported cobalt and ruthenium catalysts

被引:44
作者
Reinikainen, M
Niemelä, MK
Kakuta, N
Suhonen, S
机构
[1] VTT Chem Technol, Espoo 02044, Finland
[2] Toyohashi Univ Technol, Tempa Ku, Toyohashi, Aichi 441, Japan
[3] Tampere Univ Technol, Dept Phys, FIN-33101 Tampere, Finland
关键词
cobalt; ruthenium; catalyst preparation; CO hydrogenation; Fischer-Tropsch synthesis;
D O I
10.1016/S0926-860X(98)00155-0
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
We prepared Co/SiO2, Co-Ru/SiO2 and Ru/SiO2 catalysts by ion-exchange method in an attempt to obtain well dispersed active sites. The catalysts were characterised by chemisorption, oxygen titration, TPD and XPS, and their activity was evaluated in CO hydrogenation. The results showed that the Co/SiO2 catalyst exhibited a very low extent of reduction, and consequently its hydrogen uptake and activity were very low. In case of CoRu/SiO2, the hydrogen and CO uptake was far much higher than for the physical mixture or for the sum of Co/SiO2 and Ru/SiO2. Evidently, ruthenium acted as a reduction aid to cobalt in the bimetallic system. Yet, irrespective of the highest uptakes of the CoRu/SiO2 system, the highest activity in CO hydrogenation was obtained with the Ru/SiO2 catalyst. The synergistic performance of the CoRu catalyst was, however, evidenced by the unusually high formation of methanol - a novel finding which indicates that neither of the metals was present as a purr entity in the bimetallic system. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:61 / 75
页数:15
相关论文
共 45 条
[1]  
ANDERSSON J, 1985, INT J QUANTUM CHEM, P15
[2]  
[Anonymous], 1989, PROGR C1 CHEM, P394
[3]   HYDROGEN ADSORPTION ON SUPPORTED COBALT, IRON, AND NICKEL [J].
BARTHOLOMEW, CH .
CATALYSIS LETTERS, 1990, 7 (1-4) :27-51
[4]  
BRIGGS D, 1990, DATA ANAL XPS AES
[5]   X-RAY ABSORPTION-SPECTROSCOPY, X-RAY PHOTOELECTRON-SPECTROSCOPY, AND ANALYTICAL ELECTRON-MICROSCOPY STUDIES OF COBALT CATALYSTS .2. HYDROGEN REDUCTION PROPERTIES [J].
CASTNER, DG ;
WATSON, PR ;
CHAN, IY .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (02) :819-828
[6]   High-pressure oxidation of ruthenium as probed by surface-enhanced Raman and X-ray photoelectron spectroscopies [J].
Chan, HYH ;
Takoudis, CC ;
Weaver, MJ .
JOURNAL OF CATALYSIS, 1997, 172 (02) :336-345
[7]   EFFECTS OF ACTIVATION ON THE SURFACE-PROPERTIES OF SILICA-SUPPORTED COBALT CATALYSTS [J].
COULTER, KE ;
SAULT, AG .
JOURNAL OF CATALYSIS, 1995, 154 (01) :56-64
[8]   SUPPORTED TRANSITION-METAL COMPOUNDS .1. A NEW METHOD FOR THE PREPARATION OF ALUMINA-SUPPORTED IRIDIUM AND OSMIUM CARBONYLS [J].
CRAWFORD, JE ;
MELSON, GA ;
MAKOVSKY, LE ;
BROWN, FR .
JOURNAL OF CATALYSIS, 1983, 83 (02) :454-463
[9]   STRUCTURE SENSITIVITY AND ITS EFFECTS ON PRODUCT DISTRIBUTION IN CO HYDROGENATION ON COBALT ALUMINA [J].
FU, L ;
BARTHOLOMEW, CH .
JOURNAL OF CATALYSIS, 1985, 92 (02) :376-387
[10]   PREPARATION OF SIO2-SUPPORTED AND AL2O3-SUPPORTED CLUSTERS OF PT GROUP-METALS [J].
GONZALEZ, RD ;
MIURA, H .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1994, 36 (01) :145-177