Influence of H2S on the hydrogenation activity of relevant transition metal sulfides

被引:26
作者
Guernalec, N
Cseri, T
Raybaud, P
Geantet, C
Vrinat, M
机构
[1] Inst Rech Catalyse, F-69626 Villeurbanne, France
[2] IFP Lyon, F-69390 Vernaison, France
[3] IFP Energies Nouvelles, Div Chim & Phys Chim Appl, F-92858 Rueil Malmaison, France
关键词
transition metal sulfides; volcano curves; hydrogen disulfide; hydrogenation;
D O I
10.1016/j.cattod.2004.07.019
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Volcano curves relationships between hydrodesulfurization (HDS) or hydrogenation (HYD) catalytic activities and the ab initio calculated sulfur-metal bond energy, E(M-S), descriptor of transition metal sulfides (TMS) have been recently established. Such correlations helping to rationalize and predict the design of heterogeneous catalysts can be intuitively understood in the spirit of Sabatier principle. Similar calculations have also revealed the primary importance to better control the influence of the reaction conditions (P-H2S, P-H2, T) on such periodic trends as well as nature of the active sites. If H2S is generally considered as an inhibitor of HDS or HYD reactions, the inhibiting effect may depend on the nature of the transition metal sulfide (TMS). The observed HDS or HYD activities may thus be affected by the H2S partial pressure. The purpose of the present work is to explore the effect of H2S on the experimental catalytic activities of five relevant gamma-alumina supported TMS in toluene hydrogenation. We have undertaken a systematic kinetic study on gamma-alumina supported Rh, Ru, NiMo, Mo and Cr sulfides catalysts. Two distinct effects of H2S are evidenced. Transition metal sulfides with high and intermediate E(M-S) such as Mo, Rh, Ru and NiMo are inhibited by H2S, whereas the Cr sulfide exhibiting a low E(M-S) reveals an original promoting effect of H2S. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 66
页数:6
相关论文
共 28 条
[1]  
Aray Y, 2000, ANGEW CHEM INT EDIT, V39, P3810, DOI 10.1002/1521-3773(20001103)39:21<3810::AID-ANIE3810>3.0.CO
[2]  
2-N
[3]  
Aray Y, 2001, CHEMPHYSCHEM, V2, P599, DOI 10.1002/1439-7641(20011015)2:10<599::AID-CPHC599>3.0.CO
[4]  
2-G
[5]   Characterization of acid-base paired sites on silica-supported RuS2 by infrared spectroscopy and methyl mercaptan condensation reaction [J].
Berhault, G ;
Lacroix, M ;
Breysse, M ;
Mauge, F ;
Lavalley, JC ;
Qu, LL .
JOURNAL OF CATALYSIS, 1997, 170 (01) :37-45
[6]   VOLCANO PLOTS, HYDRODESULFURIZATION AND SURFACE ATOM PAIR POTENTIALS [J].
BURDETT, JK ;
CHUNG, JT .
SURFACE SCIENCE, 1990, 236 (1-2) :L353-L357
[7]   Periodic trends in hydrodesulfurization: in support of the Sabatier principle [J].
Chianelli, RR ;
Berhault, G ;
Raybaud, P ;
Kasztelan, S ;
Hafner, J ;
Toulhoat, H .
APPLIED CATALYSIS A-GENERAL, 2002, 227 (1-2) :83-96
[8]   Ruthenium sulphide catalysts supported on alumina: physicochemical characterization and catalytic properties in hydrotreating reactions [J].
De Los Reyes, J. A. ;
Vrinat, M. ;
Geantet, C. ;
Breysse, M. .
CATALYSIS TODAY, 1991, 10 (04) :645-664
[9]   PREPARATION AND CHARACTERIZATION OF HIGHLY-ACTIVE RUTHENIUM SULFIDE SUPPORTED CATALYSTS [J].
DELOSREYES, JA ;
GOBOLOS, S ;
VRINAT, M ;
BREYSSE, M .
CATALYSIS LETTERS, 1990, 5 (01) :17-24
[10]  
GABORIT V, 2002, CATAL TODAY, V2857, P1