Comparative study of MoS2 and Co/MoS2 catalysts prepared by ex situ in situ activation of ammonium and tetraalkylammonium thiomolybdates

被引:72
作者
Alvarez, L
Espino, J
Ornelas, C
Rico, JL
Cortez, MT
Berhault, G
Alonso, G [1 ]
机构
[1] Ctr Invest Mat Avanzados, Dept Catalisis, Chihuahua 31109, Mexico
[2] UMSNH, Fac Ingn Quim, Lab Catalisis, Inst Invest Met, Morelia 58000, Michoacan, Mexico
[3] Inst Mexicano Petr, Mexico City 07730, DF, Mexico
[4] Univ Poitiers, UMR 6503 CNRS, Catalyse Chim Organ Lab, F-86000 Poitiers, France
关键词
ex situ/in situ activation; unsupported; promotion; hydrodesulfurization; MoS2;
D O I
10.1016/j.molcata.2003.09.002
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
Ex situ and in situ decompositions of ammonium and tetraalkylammonium thiomolybdates were used to synthesize unsupported MoS2 and CoMo catalysts. The ex situ activation was performed under a H2S/H-2 flow whereas the in situ activation consists in decomposing the thiosalt precursors in the presence of a hydrocarbon solvent during the hydrodesulfurization (HDS) of dibenzothiophene (DBT). Particular attention was devoted to the use of carbon-containing precursors and to the synergetic effect of cobalt. Ammonium thiomolybdate (ATM), tetramethylammonium thiomolybdate (TMATM), and tetrapropylammonium thiomolybdate (TPATM) and their cobalt-promoted counterparts were studied. Catalysts were characterized by XRD, scanning electron microscopy (SEM) and specific surface area measurements (BET, BJH). Catalysts were evaluated for the HDS of DBT. The in situ method of preparation allows to obtain catalysts with larger superficial areas than those obtained with the ex situ method. The cobalt synergetic effect depends both on the method of activation and the presence of carbon in the precursor. For in situ activated catalysts, the promotional effect of cobalt is well-observed if carbon is present in the precursor while an opposite effect is shown for ex situ activated catalysts. (C) 2003 Elsevier B.V. All rights reserved.
引用
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页码:105 / 117
页数:13
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