Characterization of high surface area smectite supported cobalt oxides catalysts for hydrodesulfurization by means of TPR, TPS and ESR

被引:25
作者
Hayashi, E
Iwamatsu, E
Biswas, ME
Sanada, Y
Ahmed, S
Hamid, H
Yoneda, T
机构
[1] King Fahd Univ Petr & Minerals, Res Inst, Dhahran 31261, Saudi Arabia
[2] Petr Energy Ctr, Adv Catalyst Res Lab, Kanagawa, Japan
关键词
cobalt; clays; hydrodesulfurization; characterization; temperature-programed techniques;
D O I
10.1016/S0926-860X(98)00316-0
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
Catalysts of cobalt oxide loaded on smectic clays having high surface areas were prepared. Smectic clays used were montmorillonite, saponite, porous saponite, hectorite and stevensite. The catalysts were tested for hydrodesulfurization (HDS) activity with thiophene in a pulse flow reactor at different temperatures. Go-porous saponite catalyst prepared by an ion-exchange method in the series including CoMo-Al2O3 shows the highest thiophene HDS activity so far studied. The catalytic properties of the selected catalysts were characterized by temperature-programed-reduction (TPR) and -sulfiding (TPS) together with electron spin resonance (ESR). The HDS performance with thiophene is closely dependent upon the reduction temperature of cobalt oxide obtained by TPR for Co-smectite catalysts. The TPS measurements indicate that small particles of cobalt oxide are highly dispersed in the smectic layer by means of ion-exchange method. It is suggested that the properties such as sensitivity toward H2S and catalyst color of cobalt oxide on Go-porous saponite by ion-exchange method are different from those of Go-porous saponite by impregnation method. Reactivity of loaded cobalt oxide with H2S is strongly dependent upon the sulfiding paths. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:203 / 216
页数:14
相关论文
共 30 条
[1]   TEMPERATURE-PROGRAMMED SULFIDING OF MOO3/AL2O3 CATALYSTS [J].
ARNOLDY, P ;
VANDENHEIJKANT, JAM ;
DEBOK, GD ;
MOULIJN, JA .
JOURNAL OF CATALYSIS, 1985, 92 (01) :35-55
[2]   TEMPERATURE-PROGRAMMED REDUCTION OF COO/AL2O3 CATALYSTS [J].
ARNOLDY, P ;
MOULIJN, JA .
JOURNAL OF CATALYSIS, 1985, 93 (01) :38-54
[3]   COBALT-MOLYBDENUM-ALUMINA HYDRODESULPHURISATION CATALYSTS .1. A SPECTROSCOPIC AND MAGNETIC STUDY OF FRESH CATALYST AND MODEL COMPOUNDS [J].
ASHLEY, JH ;
MITCHELL, PC .
JOURNAL OF THE CHEMICAL SOCIETY A -INORGANIC PHYSICAL THEORETICAL, 1968, (11) :2821-&
[4]   THE EFFECT OF TREATMENT WITH TRIETHYLALUMINUM ON THE HYDROGENATION AND HYDRODESULFURIZATION ACTIVITY OF MOLYBDENUM, COBALT, AND NICKEL SULFIDE CATALYSTS [J].
BHADURI, M ;
MITCHELL, PCH .
JOURNAL OF CATALYSIS, 1982, 77 (01) :132-140
[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]   SURFACE SPECTROSCOPIC CHARACTERIZATION OF COBALT-ALUMINA CATALYSTS [J].
CHIN, RL ;
HERCULES, DM .
JOURNAL OF PHYSICAL CHEMISTRY, 1982, 86 (03) :360-367
[7]   SURFACE SPECTROSCOPIC CHARACTERIZATION OF COBALT MOLYBDENUM ALUMINA CATALYSTS [J].
CHIN, RL ;
HERCULES, DM .
JOURNAL OF PHYSICAL CHEMISTRY, 1982, 86 (16) :3079-3089
[8]   STUDIES ON MOLYBDENA-ALUMINA CATALYSTS .7. EFFECT OF COBALT ON CATALYST STATES AND REDUCIBILITY [J].
CHUNG, KS ;
MASSOTH, FE .
JOURNAL OF CATALYSIS, 1980, 64 (02) :320-331
[9]   THE ROLE OF COBALT AND NICKEL IN HYDRODESULFURIZATION - PROMOTERS OR CATALYSTS [J].
DEBEER, VHJ ;
DUCHET, JC ;
PRINS, R .
JOURNAL OF CATALYSIS, 1981, 72 (02) :369-372
[10]   INFLUENCE OF REDUCING AND SULFIDING TREATMENTS ON CO-AL2O3 AND MO-AL2O3 CATALYSTS - X-RAY PHOTOELECTRON-SPECTROSCOPY STUDY [J].
DECLERCKGRIMEE, RI ;
CANESSON, P ;
FRIEDMAN, RM ;
FRIPIAT, JJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1978, 82 (08) :885-888