Synthesis of CoMo-based carbon hydrodesulfurization catalysts: Influence of the order of metal impregnations on the activity

被引:17
作者
Farag, Hamdy [1 ]
机构
[1] Kyushu Univ, Dept Mat Proc Engn, Grad Sch Engn, Fukuoka 8190395, Japan
关键词
Hydrodesulfurization; Dibenzothiophene; Impregnation; Order of impregnation; Carbon;
D O I
10.1016/j.apcatb.2008.02.026
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
Series of CoMo-based carbon catalysts were synthesized via the successive impregnation method, in which the carbon material was impregnated first with cobalt. The activity of the catalysts in the hydrodesulfurization of dibenzothiophene using a high pressure batch reactor operating at 340 degrees C under 3 MPa of hydrogen was investigated. in general, the carbon-supported CoMo catalysts synthesized by the successive impregnation method (in this case cobalt was the first to be introduced) showed higher hydrodesulfurization activities for dibenzothiophene than the reference CoMo-based carbon catalyst prepared by the conventional successive impregnation. The remarkable hydrodesulfurization activities of these CoMo-based carbon catalysts are suggested to be a consequence of forming a new synergy between molybdenum and cobalt. The data provide evidence that the CoMo-bimetallic synergy is affected by the nature of the support and by the order of metal impregnation. The results support the view of the electronic origin of such synergy. (c) 2008 Elsevier B.V. All rights reserved
引用
收藏
页码:1 / 8
页数:8
相关论文
共 40 条
[1]   TEMPERATURE-PROGRAMMED SULFIDING AND REDUCTION OF COO/AL2O3 CATALYSTS [J].
ARNOLDY, P ;
DEBOOYS, JL ;
SCHEFFER, B ;
MOULIJN, JA .
JOURNAL OF CATALYSIS, 1985, 96 (01) :122-138
[2]   Search for an efficient 4,6-DMDBT hydrodesulfurization catalyst: A review of recent studies [J].
Bej, SK ;
Maity, SK ;
Turaga, UT .
ENERGY & FUELS, 2004, 18 (05) :1227-1237
[3]   Deep desulfurization:: reactions, catalysts and technological challenges [J].
Breysse, M ;
Djega-Mariadassou, G ;
Pessayre, S ;
Geantet, C ;
Vrinat, M ;
Pérot, G ;
Lemaire, M .
CATALYSIS TODAY, 2003, 84 (3-4) :129-138
[4]   Periodic trends transition metal sulfide catalysis: Intuition and theory [J].
Chianelli, R. R. .
OIL & GAS SCIENCE AND TECHNOLOGY-REVUE D IFP ENERGIES NOUVELLES, 2006, 61 (04) :503-513
[5]   Symmetrical synergism and the role of carbon in transition metal sulfide catalytic materials [J].
Chianelli, RR ;
Berhault, G .
CATALYSIS TODAY, 1999, 53 (03) :357-366
[6]   Surface science models for CoMo hydrodesulfurization catalysts: Influence of the support on hydrodesulfurization activity [J].
Coulier, L ;
Kishan, G ;
van Veen, JAR ;
Niemantsverdriet, JW .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 2001, 19 (04) :1510-1515
[7]   On the formation of cobalt-molybdenum sulfides in silica-supported hydrotreating model catalysts [J].
Coulier, L ;
de Beer, VHJ ;
van Veen, JAR ;
Niemantsverdriet, JW .
TOPICS IN CATALYSIS, 2000, 13 (1-2) :99-108
[8]  
DEBEER VHJ, 1976, J CATAL, V43, P78
[9]   X-RAY PHOTOELECTRON-SPECTROSCOPY STUDY OF VARIOUS COMO-AL2O3 HYDRODESULFURIZATION CATALYSTS [J].
DECLERCKGRIMEE, RI ;
CANESSON, P ;
FRIEDMAN, RM ;
FRIPIAT, JJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1978, 82 (08) :889-894
[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