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
[11]   CARBON-SUPPORTED SULFIDE CATALYSTS [J].
DUCHET, JC ;
VANOERS, EM ;
DEBEER, VHJ ;
PRINS, R .
JOURNAL OF CATALYSIS, 1983, 80 (02) :386-402
[12]  
EPA, 2003, RED NONR DIES EM, P101
[13]   Fundamental comparison studies on hydrodesulfurization of dibenzothiophenes over CoMo-based carbon and alumina catalysts [J].
Farag, H ;
Mochida, I ;
Sakanishi, K .
APPLIED CATALYSIS A-GENERAL, 2000, 194 :147-157
[14]   Synthesis of active hydrodesulfurization carbon-supported Co-Mo catalysts. Relationships between preparation methods and activity/selectivity [J].
Farag, H ;
Whitehurst, DD ;
Mochida, I .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1998, 37 (09) :3533-3539
[15]   Effect of sulfidation temperatures on the bulk structures of various molybdenum precursors [J].
Farag, H .
ENERGY & FUELS, 2002, 16 (04) :944-950
[16]   Selective adsorption of refractory sulfur species on active carbons and carbon based CoMo catalyst [J].
Farag, Hamdy .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2007, 307 (01) :1-8
[17]   Urea-organic matrix method:: an alternative approach to prepare CO-MoS2/γ-Al2O3 HDS catalyst [J].
González-Cortés, SL ;
Xiao, TC ;
Costa, PMFJ ;
Fontal, B ;
Green, MLH .
APPLIED CATALYSIS A-GENERAL, 2004, 270 (1-2) :209-222
[18]   Reaction pathways on NiMo/Al2O3 catalysts for hydrodesulfurization of diesel fuel [J].
Kagami, N ;
Vogelaar, BM ;
van Langeveld, AD ;
Moulijn, JA .
APPLIED CATALYSIS A-GENERAL, 2005, 293 :11-23
[19]   Carbon-supported Mo catalysts prepared by a new impregnation method using a MoO3/water slurry:: saturated loading, hydrodesulfurization activity and promotion by Co [J].
Kaluza, L ;
Zdrazil, M .
CARBON, 2001, 39 (13) :2023-2034
[20]   SYNERGY BETWEEN THE COMOS PHASE AND SUPPORTED OR UNSUPPORTED COBALT SULFIDE - EXISTENCE OF A REMOTE-CONTROL EFFECT [J].
KARROUA, M ;
MATRALIS, H ;
SHAM, E ;
GRANGE, P ;
DELMON, B .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1995, 68 (01) :107-119