Influence of the impregnation order of molybdenum and cobalt in carbon-supported catalysts for hydrodeoxygenation reactions

被引:75
作者
Ferrari, M [1 ]
Delmon, B [1 ]
Grange, P [1 ]
机构
[1] Univ Catholique Louvain, Unite Catalyse & Chim Mat Divises, B-1348 Louvain, Belgium
关键词
activated carbon; catalytic properties;
D O I
10.1016/S0008-6223(01)00128-2
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
Four activated carbons were used as supports and the effect of the impregnation order (either cobalt or molybdenum first) was considered and tested in hydrodeoxygenation reactions. Both series of samples exhibit a preferential impregnation of the metal oxides at the exterior of the carbon grains, but CoMo (molybdenum first) is more uniformly distributed than MoCo (cobalt first). When molybdenum is added after cobalt (MoCo), the molybdenum-cobalt interactions cause a thick layer of metal oxide crystals to be formed; it covers the external grain surface and it is only in partial physical contact with the carrier. When cobalt is added after molybdenum (CoMo), it seems to bring about the remobilization and migration of molybdenum to the external part of the grains. Finally it is shown that inorganic impurities, like calcium and iron, which are present in low amounts in the activated carbon can interact with molybdenum and form mixed oxides. Concerning the catalytic activity, MoCo catalysts show lower hydrogenation properties for the conversion of ketonic groups and lower decarboxylation selectivity in the conversion of the ester. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:497 / 511
页数:15
相关论文
共 33 条
[1]   A REVIEW OF CARBON-SUPPORTED HYDRODESULFURIZATION CATALYSTS [J].
ABOTSI, GMK ;
SCARONI, AW .
FUEL PROCESSING TECHNOLOGY, 1989, 22 (02) :107-133
[2]   A COMPARISON OF ALUMINA, CARBON AND CARBON-COVERED ALUMINA AS SUPPORTS FOR NI-MO-F ADDITIVES - GAS OIL HYDROPROCESSING STUDIES [J].
BOORMAN, PM ;
KYDD, RA ;
SORENSEN, TS ;
CHONG, K ;
LEWIS, JM ;
BELL, WS .
FUEL, 1992, 71 (01) :87-93
[3]   Effect of surface oxidation of the support on the thiophene hydrodesulfurization activity of Mo, Ni, and NiMo catalysts supported on activated carbon [J].
Calafat, A ;
Laine, J ;
LopezAgudo, A ;
Palacios, JM .
JOURNAL OF CATALYSIS, 1996, 162 (01) :20-30
[4]   INFLUENCE OF THE SUPPORT OF COMO SULFIDE CATALYSTS AND OF THE ADDITION OF POTASSIUM AND PLATINUM ON THE CATALYTIC PERFORMANCES FOR THE HYDRODEOXYGENATION OF CARBONYL, CARBOXYL, AND GUAIACOL-TYPE MOLECULES [J].
CENTENO, A ;
LAURENT, E ;
DELMON, B .
JOURNAL OF CATALYSIS, 1995, 154 (02) :288-298
[5]  
CENTENO A, 1997, THESIS UCL BELGIUM
[6]   Interactions between molybdenum and activated carbons on the preparation of activated carbon-supported molybdenum catalysts [J].
de la Puente, G ;
Centeno, A ;
Gil, A ;
Grange, P .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1998, 202 (01) :155-166
[7]   Effects of support surface chemistry in hydrodeoxygenation reactions over CoMo/activated carbon sulfided catalysts [J].
de la Puente, G ;
Gil, A ;
Pis, JJ ;
Grange, P .
LANGMUIR, 1999, 15 (18) :5800-5806
[8]   HYDRODESULFURIZATION ACTIVITY AND COKING PROPENSITY OF CARBON AND ALUMINA SUPPORTED CATALYSTS [J].
DEBEER, VHJ ;
DERBYSHIRE, FJ ;
GROOT, CK ;
PRINS, R ;
SCARONI, AW ;
SOLAR, JM .
FUEL, 1984, 63 (08) :1095-1100
[9]  
DELANNAY F, 1978, J MICROSC SPECT ELEC, V3, P411
[10]  
DELANNAY F, 1980, B SOC CHIM BELG, V89, P255