Interactions between molybdenum and activated carbons on the preparation of activated carbon-supported molybdenum catalysts

被引:37
|
作者
de la Puente, G
Centeno, A
Gil, A
Grange, P
机构
[1] Univ Catholique Louvain, Unite Catalyse & Chim Mat Divises, B-1348 Louvain, Belgium
[2] CSIC, Inst Nacl Carbon, E-33080 Oviedo, Spain
[3] Univ Publ Navarra, Dept Quim Aplicada, Pamplona 31006, Spain
关键词
activated carbon oxidation; activated carbon-supported molybdenum catalysts; textural properties; surface characterization; surface oxygen groups;
D O I
10.1006/jcis.1998.5461
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 influence of the porous texture and surface chemistry of an activated carbon on the preparation of activated carbon-supported molybdenum catalysts was studied, Activated carbons with various degrees of oxidation were used as supports. Supports and catalysts were characterized by nitrogen adsorption at 77 K, temperature-programmed desorption (TPD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS), The impregnation with molybdenum produced a reduction of the textural properties. TPD results indicated that there was a transformation of CO2- and CO-evolving oxygen functional groups on the activated carbon as a consequence of the impregnation of molybdenum and that acidic groups were acting as chemical anchorage centers, FTIR and XPS analyses confirmed that interactions were established between molybdenum species and carbonyl and ether surface functional groups. These results indicate that the molybdenum was well distributed and reached the inner porous network of the carbon support. (C) 1998 Academic Press.
引用
收藏
页码:155 / 166
页数:12
相关论文
共 50 条
  • [1] Studies of activated carbon-supported molybdenum-nickel catalysts for hydrodesulfurization
    Truszkiewicz, Elzbieta
    Rarog-Pilecka, Wioletta
    Irach, Michal
    Iwanek, Ewa
    Narowski, Ryszard
    Kowalczyk, Zbigniew
    PRZEMYSL CHEMICZNY, 2011, 90 (06): : 1232 - 1236
  • [2] On the distribution of oxygen-containing surface groups in carbons and their influence on the preparation of carbon-supported molybdenum catalysts
    de la Puente, G
    Menendez, JA
    SOLID STATE IONICS, 1998, 112 (1-2) : 103 - 111
  • [3] EFFECT OF CARBON PROPERTIES ON THE PREPARATION AND ACTIVITY OF CARBON-SUPPORTED MOLYBDENUM SULFIDE CATALYSTS
    MARTINGULLON, A
    PRADOBURGUETE, C
    RODRIGUEZREINOSO, F
    CARBON, 1993, 31 (07) : 1099 - 1105
  • [4] Alcohol synthesis over pre-reduced activated carbon-supported molybdenum-based catalysts
    Li, XG
    Feng, LJ
    Zhang, LJ
    Dadyburjor, DB
    Kugler, EL
    MOLECULES, 2003, 8 (01) : 13 - 30
  • [5] EFFECTS OF SURFACE AND STRUCTURAL-PROPERTIES OF CARBONS ON THE BEHAVIOR OF CARBON-SUPPORTED MOLYBDENUM CATALYSTS
    SOLAR, JM
    DERBYSHIRE, FJ
    DEBEER, VHJ
    RADOVIC, LR
    JOURNAL OF CATALYSIS, 1991, 129 (02) : 330 - 342
  • [6] SULFIDATION OF CARBON-SUPPORTED IRON - MOLYBDENUM OXIDE CATALYSTS
    RAMSELAAR, WLTM
    CRAJE, MWJ
    GERKEMA, E
    DEBEER, VHJ
    VANDERKRAAN, AM
    APPLIED CATALYSIS, 1989, 54 (03): : 217 - 239
  • [7] How do the graphenic domains terminate in activated carbons and carbon-supported metal catalysts?
    Vottero, Eleonora
    Carosso, Michele
    Jimenez-Ruiz, Monica
    Pellegrini, Riccardo
    Groppo, Elena
    Piovano, Andrea
    CARBON, 2020, 169 : 357 - 369
  • [8] CHARACTERISTICS OF BIMETALLIC COBALT AND MOLYBDENUM CATALYSTS SUPPORTED ON ACTIVATED CARBON OR ALUMINA IN HYDRODESULFURIZATION
    MOON, SJ
    IHM, SK
    KOREAN JOURNAL OF CHEMICAL ENGINEERING, 1994, 11 (02) : 111 - 118
  • [9] Selective hydrodeoxygenation of guaiacol to phenolics over activated carbon supported molybdenum catalysts
    Cai, Zhe
    Wang, Fumin
    Zhang, Xubin
    Ahishakiye, Rosine
    Xie, Yi
    Shen, Yu
    MOLECULAR CATALYSIS, 2017, 441 : 28 - 34
  • [10] Carbon-Supported Molybdenum Carbide Catalysts for the Conversion of Vegetable Oils
    Han, Junxing
    Duan, Jinzhao
    Chen, Ping
    Lou, Hui
    Zheng, Xiaoming
    Hong, Haiping
    CHEMSUSCHEM, 2012, 5 (04) : 727 - 733