WS2 catalysts from tetraalkyl thiotungstate precursors and their concurrent in situ activation during HDS of DBT

被引:25
作者
Alonso, G
Chianelli, RR
机构
[1] Ctr Invest Mat Avanzados, Dept Catalisis, Chih 31109, Mexico
[2] Univ Texas, Mat Res Technol Inst, El Paso, TX 79968 USA
关键词
in situ activated; WS2; catalysts; tetraalkyl thiometallates;
D O I
10.1016/j.jcat.2003.10.003
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
The synthesis of tetraalkylammonium thiotungstates (R4N)(2)WS4 {R-4 = tetraheptyl or cetyltrimethyl}, using an aqueous solution method is reported. Tetraheptylammonium thiotungstate and cetyltrimethylammonium thiotungstate were synthesized and characterized using FTIR, UV, and TGA-DTA. These thiosalts precursors were in situ-activated concurrently during hydrodesulfurization (HDS) of dibenzothiophene (DBT), producing WS2 catalysts. These catalysts were analyzed by X-ray diffraction and surface area. The nature of the alkyl group affects both the surface area and the HDS selectivity. The X-ray diffraction study showed that the catalysts are poorly crystalline, with a very weak intensity of (002). (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:657 / 661
页数:5
相关论文
共 21 条
[1]   Synthesis and characterization of tetraalkylammonium thiomolybdates and thiotungstates in aqueous solution [J].
Alonso, G ;
Aguirre, G ;
Rivero, IA ;
Fuentes, S .
INORGANICA CHIMICA ACTA, 1998, 274 (01) :108-110
[2]   Characterization and HDS activity of mesoporous MoS2 catalysts prepared by in situ activation of tetraalkylammonium thiomolybdates [J].
Alonso, G ;
Berhault, G ;
Aguilar, A ;
Collins, V ;
Ornelas, C ;
Fuentes, S ;
Chianelli, RR .
JOURNAL OF CATALYSIS, 2002, 208 (02) :359-369
[3]   Preparation of MoS2 and WS2 catalysts by in situ decomposition of ammonium thiosalts [J].
Alonso, G ;
Del Valle, M ;
Cruz, J ;
Licea-Claverie, A ;
Petranovskii, V ;
Fuentes, S .
CATALYSIS LETTERS, 1998, 52 (1-2) :55-61
[4]   THERMAL AND REDUCTIVE DECOMPOSITION OF AMMONIUM THIOMOLYBDATES [J].
BRITO, JL ;
ILIJA, M ;
HERNANDEZ, P .
THERMOCHIMICA ACTA, 1995, 256 (02) :325-338
[5]   THE ORIGIN OF CATALYTIC SYNERGY IN UNSUPPORTED CO-MO HDS CATALYSTS [J].
CANDIA, R ;
CLAUSEN, BS ;
TOPSOE, H .
JOURNAL OF CATALYSIS, 1982, 77 (02) :564-566
[6]  
Chianelli R.R., 1985, U.S. Patent, Patent No. [4508847, 4,508,847]
[7]   LOW-TEMPERATURE SOLUTION PREPARATION OF GROUP 4B, 5B, AND 6B TRANSITION-METAL DICHALCOGENIDES [J].
CHIANELLI, RR ;
DINES, MB .
INORGANIC CHEMISTRY, 1978, 17 (10) :2758-2762
[8]   STRUCTURE-FUNCTION RELATIONS IN MOLYBDENUM SULFIDE CATALYSTS - THE RIM-EDGE MODEL [J].
DAAGE, M ;
CHIANELLI, RR .
JOURNAL OF CATALYSIS, 1994, 149 (02) :414-427
[9]   PHYSIOCHEMICAL INVESTIGATIONS AND CATALYTIC ACTIVITY MEASUREMENTS ON CRYSTALLIZED MOLYBDENUM SULFIDE COBALT SULFIDE MIXED CATALYSTS [J].
HAGENBAC.G ;
COURTY, P ;
DELMON, B .
JOURNAL OF CATALYSIS, 1973, 31 (02) :264-273
[10]   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