CoMo/alumina prepared from carbonyl precursors DRIFT, TPR and HDS studies

被引:8
作者
Kurhinen, M [1 ]
Pakkanen, TA [1 ]
机构
[1] Univ Joensuu, Dept Chem, FIN-80101 Joensuu, Finland
基金
芬兰科学院;
关键词
Mo(CO)(6); Co-2(CO)(8); alumina; gas phase deposition; IR; TPR; HDS;
D O I
10.1016/S0926-860X(99)00335-X
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 [物理化学]; 081704 [应用化学];
摘要
Mo(CO)(6) was deposited on alumina by gas phase adsorption in a fluidised bed reactor. Samples were heated gradually to determine the thermal behaviour of the surface species of molybdenum carbonyls. Mo(CO)(3)(ads) was identified as the most stable species, evidently appearing as two adsorption sites of different thermal stability. The IR spectrum recorded after deposition of Co-2(CO)(8) on Mo/alumina was the same as the IR spectrum of Co-2(CO)(8) on alumina. After decarbonylation at 200 degrees C, the nu(CO) bands due to the less stable of the Mo(CO)(3)(ads) species were better resolved when Mo(CO)(6) was deposited after decarbonylation of Co-2(CO)(8) on alumina, than when it was directly deposited on alumina. temperature-programmed reduction demonstrated interactions between alumina supported molybdenum and cobalt species. Activity of the samples was tested in hydrodesulphurisation of thiophene using a batch reactor. n-Butane was the main product, and the thiophene conversion was found to depend on the deposition order of the metals when the concentrations of the metals were similar. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 103
页数:7
相关论文
共 29 条
[1]
THERMAL-REACTIONS OF MO(CO)(6) ON METAL-OXIDE SURFACES [J].
ANG, HG ;
CHAN, KS ;
CHUAH, GK ;
JAENICKE, S ;
NEO, SK .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1995, (23) :3753-3758
[2]
ON THE STRUCTURAL DIFFERENCES BETWEEN ALUMINA-SUPPORTED COMOS TYPE-I AND ALUMINA-SUPPORTED, SILICA-SUPPORTED, AND CARBON-SUPPORTED COMOS TYPE-II PHASES STUDIED BY XAFS, MES, AND XPS [J].
BOUWENS, SMAM ;
VANZON, FBM ;
VANDIJK, MP ;
VANDERKRAAN, AM ;
DEBEER, VHJ ;
VANVEEN, JAR ;
KONINGSBERGER, DC .
JOURNAL OF CATALYSIS, 1994, 146 (02) :375-393
[3]
BRATERMAN PS, 1975, METAL CARBONYL SPECT, P177
[4]
CLUSTERS AND CATALYSIS - ON THE REQUIREMENT FOR MULTI-NUCLEAR CENTERS TO CATALYZE THE HYDROGENATION OF CARBON-MONOXIDE [J].
BRENNER, A ;
HUCUL, DA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (07) :2484-2487
[5]
INTRAZEOLITE CHEMISTRY OF COBALT CARBONYLS [J].
CONNAWAY, MC ;
HANSON, BE .
INORGANIC CHEMISTRY, 1986, 25 (09) :1445-1451
[6]
SYNTHESIS AND ACTIVITY OF HYDROTREATING CATALYSTS PREPARED VIA PROMOTION BY LOW-VALENT TRANSITION-METAL COMPLEXES [J].
HALBERT, TR ;
HO, TC ;
STIEFEL, EI ;
CHIANELLI, RR ;
DAAGE, M .
JOURNAL OF CATALYSIS, 1991, 130 (01) :116-129
[7]
INFRARED-SPECTRA AND CATALYTIC ACTIVITY OF SUPPORTED MOLYBDENUM HEXACARBONYL [J].
HOWE, RF ;
DAVIDSON, DE ;
WHAN, DA .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1972, 68 (12) :2266-&
[8]
INFRARED EVIDENCE FOR REVERSIBILITY IN FORMATION OF SURFACE CARBONYL-COMPLEXES [J].
HOWE, RF .
INORGANIC CHEMISTRY, 1976, 15 (02) :486-488
[9]
HYDRODESULFURIZATION OF DIBENZOTHIOPHENE CATALYZED BY SILICA-ALUMINA SUPPORTED ANIONIC MOLYBDENUM CARBONYL-COMPLEXES [J].
ISHIHARA, A ;
SHIROUCHI, K ;
KABE, T .
CHEMISTRY LETTERS, 1993, (04) :589-592
[10]
Ruthenium promotion of Co/Al2O3 Fischer-Tropsch catalysts [J].
Kogelbauer, A ;
Goodwin, JG ;
Oukaci, R .
JOURNAL OF CATALYSIS, 1996, 160 (01) :125-133