The catalytic activity of platinum-loaded porous smectite-like clay minerals containing different divalent cations for butane hydrogenolysis and ethylene hydrogenation

被引:31
作者
Arai, M [1 ]
Guo, SL [1 ]
Shirai, M [1 ]
Nishiyama, Y [1 ]
Torii, K [1 ]
机构
[1] NATL IND RES INST TOHOKU,MIYAGINO KU,SENDAI,MIYAGI 983,JAPAN
关键词
D O I
10.1006/jcat.1996.0232
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
Supported platinum catalysts were prepared using newly synthesized porous smectite-like clay minerals containing different divalent cations of Ni2+, C2+, Mg2+, and Zn2+ in trioctahedral sheets. Platinum was loaded on the clay minerals through the adsorption of metal precursors followed by the reduction with hydrogen. The activities of the catalysts prepared for n-butane hydrogenolysis and ethylene hydrogenation were shown to depend significantly on the support used, being in the order of Pt/SM (Ni) > Pt/SM(Co), Pt/SM(Mg) >> Pt/SM(Zn), where SM(M) denotes the smectite-like clay mineral containing M(2+) cation. The former three catalysts are much more active compared with a control Pt/SiO2 catalyst. The Pt/SM(Zn) catalyst is inactive, probably due to a toxic effect of Zn2+ on platinum. The high catalytic activities observed may be explained by high degrees of platinum dispersion for Pt/SM(Co) and Pt/SM(Mg) catalysts. The highest activity of Pt/SM(Ni) catalyst may be attributable to the presence of different reactive-sites more active than platinum. These active sites are reduced nickel species arising from the support, which are produced by platinum-catalyzed hydrogen reduction. (C) 1996 Academic Press, Inc.
引用
收藏
页码:704 / 712
页数:9
相关论文
共 26 条
[1]  
ANDERSON JR, 1975, STRUCTURE METALLIC C, P74
[2]   IMPORTANCE OF SURFACE HYDROXYL-GROUPS TO THE DISPERSION OF NICKEL IMPREGNATED ON SILICA-GELS [J].
ARAI, M ;
GUO, SL ;
NISHIYAMI, Y .
JOURNAL OF CATALYSIS, 1992, 135 (02) :638-641
[3]   THE DISTRIBUTION OF ACTIVATION-ENERGY FOR HYDROGEN DESORPTION OVER SILICA-SUPPORTED NICKEL-CATALYSTS DETERMINED FROM TEMPERATURE-PROGRAMMED DESORPTION SPECTRA [J].
ARAI, M ;
NISHIYAMA, Y ;
MASUDA, T ;
HASHIMOTO, K .
APPLIED SURFACE SCIENCE, 1995, 89 (01) :11-19
[4]   CHARACTERIZATION OF SILICA-SUPPORTED NICKEL-CATALYSTS BY THE TEMPERATURE-PROGRAMMED DESORPTION OF HYDROGEN ADSORBED AT VARIOUS TEMPERATURES [J].
ARAI, M ;
SUZUKI, K ;
NISHIYAMA, Y .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1993, 66 (01) :40-45
[5]  
Boudart M., 1984, KINETICS HETEROGENEO, P26
[6]  
Cerveny L., 1986, STUD SURF SCI CATAL, V27, P145
[7]   DISSOLUTION KINETICS OF SEPIOLITE FROM ESKISEHIR (TURKEY) IN HYDROCHLORIC AND NITRIC-ACIDS [J].
CETISLI, H ;
GEDIKBEY, T .
CLAY MINERALS, 1990, 25 (02) :207-215
[8]   RELAXATION AND STABILITY OF SMALL TRANSITION-METAL PARTICLES [J].
GORDON, MB ;
CYROTLACKMANN, F ;
DESJONQUERES, MC .
SURFACE SCIENCE, 1979, 80 (01) :159-164
[9]   EXAFS STUDY OF THE INFLUENCE OF HYDROGEN DESORPTION AND OXYGEN-ADSORPTION ON THE STRUCTURAL-PROPERTIES OF SMALL IRIDIUM PARTICLES SUPPORTED ON AL2O3 [J].
KAMPERS, FWH ;
KONINGSBERGER, DC .
FARADAY DISCUSSIONS, 1990, 89 :137-141
[10]   ACID-HYDROLYSIS OF OCTAHEDRAL MG2+ SITES IN 2/1 LAYERED SILICATES - AN ASSESSMENT OF EDGE ATTACK AND GALLERY ACCESS MECHANISMS [J].
KAVIRATNA, H ;
PINNAVAIA, TJ .
CLAYS AND CLAY MINERALS, 1994, 42 (06) :717-723