Cobalt molybdenum carbides: Surface properties and reactivity for methane decomposition

被引:40
作者
Izhar, Shamsul [1 ]
Kanesugi, Hiroyuki [1 ]
Tominaga, Hiroyuki [1 ]
Nagai, Masatoshi [1 ]
机构
[1] Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, Koganei, Tokyo 1848588, Japan
关键词
Co-Mo; carbide; methane decomposition; TPC; XRD; TPR; XPS;
D O I
10.1016/j.apcata.2006.10.013
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 methane decomposition over cobalt molybdenum catalysts (CoMo100-x; x = 0, 25, 50, and 75) carburized at temperatures of 700-973 K was performed using a microreactor at 973 K. The active species for the production of hydrogen during the methane decomposition was studied on the basis of XRD, TPC, TPR, and XPS. The Co50W50C-800 catalyst exhibits a higher conversion and hydrogen production rate compared to the Mo100C-, Co25Mo75C-, and Co75Mo25C-800 catalysts. The XRD measurement showed the presence of beta-Mo2C and cobalt molybdenum oxycarbides in the catalyst before and after 6-h reaction. Cobalt molybdenum carbutized at 800 K produced a surface oxycarbide based on the formation of H2O during the TPC and production of CH4 and H2O during the TPR. The active species of the cobalt molybdenum carbide catalyst for the CH4 decomposition was the cobalt molybdenum oxycarbide (Co1.0Mo5.6C0.3O0.7 by XPS analysis) on the surface that was formed during the carburization. The catalyst also exhibited a longer lifetime during methane decomposition. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:82 / 90
页数:9
相关论文
共 25 条
  • [1] Comparison of bulk CoMo bimetallic carbide, oxide, nitride and sulfide catalysts for pyridine hydrodenitrogenation
    Al-Megren, HA
    Xiao, T
    Gonzalez-Cortes, SL
    Al-Khowaiter, SH
    Green, MLH
    [J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2005, 225 (02) : 143 - 148
  • [2] Cobalt catalysts of methane decomposition: accumulation of the filamentous carbon
    Avdeeva, LB
    Kochubey, DI
    Shaikhutdinov, SK
    [J]. APPLIED CATALYSIS A-GENERAL, 1999, 177 (01) : 43 - 51
  • [3] INFLUENCE OF MOLYBDENUM AND TUNGSTEN ADDITIVES ON THE PROPERTIES OF NICKEL STEAM REFORMING CATALYSTS
    BOROWIECKI, T
    GOLEBIOWSKI, A
    [J]. CATALYSIS LETTERS, 1994, 25 (3-4) : 309 - 313
  • [4] Microstructure and characterization of a highly selective catalyst for the isomerization of alkanes: A molybdenum oxycarbide
    Bouchy, C
    Pham-Huu, C
    Heinrich, B
    Chaumont, C
    Ledoux, MJ
    [J]. JOURNAL OF CATALYSIS, 2000, 190 (01) : 92 - 103
  • [5] New catalysts for the conversion of methane to synthesis gas: Molybdenum and tungsten carbide
    Claridge, JB
    York, APE
    Brungs, AJ
    Marquez-Alvarez, C
    Sloan, J
    Tsang, SC
    Green, MLH
    [J]. JOURNAL OF CATALYSIS, 1998, 180 (01) : 85 - 100
  • [6] Characterization and HDS activity of cobalt molybdenum nitrides
    Hada, K
    Nagai, M
    Omi, S
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (19) : 4084 - 4093
  • [7] XPS and TPR studies of nitrided molybdena-alumina
    Hada, K
    Nagai, M
    Omi, S
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (09): : 2090 - 2098
  • [8] Relationship between the structure/composition of Co-Mo catalysts and their ability to produce single-walled carbon nanotubes by CO disproportionation
    Herrera, JE
    Balzano, L
    Borgna, A
    Alvarez, WE
    Resasco, DE
    [J]. JOURNAL OF CATALYSIS, 2001, 204 (01) : 129 - 145
  • [9] Carbon deposition on Ni/Al2O3 catalysts doped with small amounts of molybdenum
    Kepinski, L
    Stasinska, B
    Borowiecki, T
    [J]. CARBON, 2000, 38 (13) : 1845 - 1856
  • [10] COMPARED ACTIVITIES OF PLATINUM AND HIGH SPECIFIC SURFACE-AREA MO2C AND WC CATALYSTS FOR REFORMING REACTIONS .1. CATALYST ACTIVATION AND STABILIZATION - REACTION OF NORMAL-HEXANE
    LEDOUX, MJ
    CUONG, PH
    GUILLE, J
    DUNLOP, H
    [J]. JOURNAL OF CATALYSIS, 1992, 134 (02) : 383 - 398