The role of titania in supported Mo, CoMo, NiMo, and NiW hydrodesulfurization catalysts:: analysis of past and new evidences

被引:132
作者
Ramírez, J
Macías, G
Cedeño, L
Gutiérrez-Alejandre, A
Cuevas, R
Castillo, P
机构
[1] Univ Nacl Autonoma Mexico, Fac Quim, UNICAT, Dept Ingn Quim, Mexico City 04510, DF, Mexico
[2] Inst Mexicano Petr, Mexico City 07730, DF, Mexico
关键词
titania; titania-alumina; hydrodesulfurization catalysts; mixed oxide supports; CoMo; NiMo; NiW; thiophene; DBT; 4,6-DMDBT; naphthalene hydrogenation;
D O I
10.1016/j.cattod.2004.07.050
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Previous results and new evidence on the role of titania in supported hydrodesulfurization catalysts are analyzed in order to construct a rational explanation for the different findings in Ti-containing HDS catalysts. Some of the important findings follow. The preparation method of Al-Ti oxide supports is important to catalytic activity. It is not the total amount of Ti but the Ti oxide surface structures that is relevant. TiO2 is an electronic promoter in HDS catalysts. Ti3+ species formed under HDS reaction conditions act as electron donors. These electrons can be easily transferred, through the conduction band of the support, and be injected to the Mo 3d conduction band. This causes a weakening of the Mo-S bonds and helps the creation of more CUS. The addition of TiO2 to the surface of alumina eliminates the most reactive surface hydroxyl groups and avoids the formation of tetrahedral Mo oxide species, causing an increase of well-sulfided active phase and hence in catalytic activity. This effect, although significant, is less important than the electronic promotion of Mo by Ti. TiO2-containing catalysts are well suited for deep HDS because they facilitate the formation of a greater number of CUS in MoS2 (or WS2), favoring the hydrogenation-hydrodesulfurization route of transformation of 4,6-DMDBT. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 30
页数:12
相关论文
共 53 条
[21]   CATALYSIS BY TRANSITION-METAL SULFIDES - A THEORETICAL AND EXPERIMENTAL-STUDY OF THE RELATION BETWEEN THE SYNERGIC SYSTEMS AND THE BINARY TRANSITION-METAL SULFIDES [J].
HARRIS, S ;
CHIANELLI, RR .
JOURNAL OF CATALYSIS, 1986, 98 (01) :17-31
[22]   CATALYSIS BY TRANSITION-METAL SULFIDES - THE RELATION BETWEEN CALCULATED ELECTRONIC TRENDS AND HDS ACTIVITY [J].
HARRIS, S ;
CHIANELLI, RR .
JOURNAL OF CATALYSIS, 1984, 86 (02) :400-412
[23]   Catalyst and process technologies for ultra low sulfur diesel [J].
Knudsen, KG ;
Cooper, BH ;
Topsoe, H .
APPLIED CATALYSIS A-GENERAL, 1999, 189 (02) :205-215
[24]   Hydrodesulfurization of methyl-substituted dibenzothiophenes: Fundamental study of routes to deep desulfurization [J].
Landau, MV ;
Berger, D ;
Herskowitz, M .
JOURNAL OF CATALYSIS, 1996, 159 (01) :236-245
[25]   Deep hydrotreating of middle distillates from crude and shale oils [J].
Landau, MV .
CATALYSIS TODAY, 1997, 36 (04) :393-429
[26]   Hydrodesulfurization activity of CoMo and NiMo supported on Al2O3-TiO2 for some model compounds and gas oils [J].
Lecrenay, E ;
Sakanishi, K ;
Nagamatsu, T ;
Mochida, I ;
Suzuka, T .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (3-4) :325-330
[27]   The sulfidation of gamma-alumina and titania supported (cobalt)molybdenum oxide catalysts monitored by EXAFS [J].
Leliveld, RG ;
vanDillen, AJ ;
Geus, JW ;
Koningsberger, DC .
JOURNAL OF CATALYSIS, 1997, 171 (01) :115-129
[28]   Characterization of titanium-containing mesoporous silica molecular sieve SBA-15 and generation of paramagnetic hole and electron centers [J].
Luan, ZH ;
Kevan, L .
MICROPOROUS AND MESOPOROUS MATERIALS, 2001, 44 (44-45) :337-344
[29]   TEMPERATURE DEPENDENCES OF ELECTRICAL AND ELECTROCHEMICAL PROPERTIES OF TITANIUM DISULFIDE [J].
MOLENDA, J .
JOURNAL OF THERMAL ANALYSIS, 1992, 38 (09) :2163-2169
[30]   Materials aspects of titanium-doped aluminas:: 14%Ti/γ-Al2O3/Cu and sulfided Al2O3-TiO2/NiMo [J].
Öhman, LO ;
Paul, J .
MATERIALS CHEMISTRY AND PHYSICS, 2002, 73 (2-3) :242-251