Reactivity of carbon species formed on supported noble metal catalysts in methane conversion reactions

被引:20
|
作者
Matsui, N [1 ]
Nakagawa, K [1 ]
Ikenaga, N [1 ]
Suzuki, T [1 ]
机构
[1] Kansai Univ, High Technol Res Ctr, Suita, Osaka 5648680, Japan
基金
日本学术振兴会;
关键词
temperature-programmed reaction; temperature-programmed oxidation; ruthenium; rhodium; iridium; lanthanum oxide;
D O I
10.1006/jcat.2000.2920
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 reactivity of carbon species formed from methane decomposition over supported noble metal catalysts was examined. In the Ru-loaded case, the rate of formation of CHx species in the decomposition of CH4 and the amount of CHx species over Ru are independent of the type of support. However, the carbon species on Ru/La2O3 seems to be more uniform and reactive than that on Ru/Al2O3. After the decomposition of CH4 over Ru-loaded catalysts was carried out at 700 degrees C, a temperature-programmed reaction with D-2 was carried out. CD4 was the major product on all the supports, and only slight amounts of CH3D, CH2D2, and CHD3 were detected over La2O3, ZrO2, and Y2O3 supports. The reactivity of CHx species on Ru strongly depends on the supports. The reactivity of CHx species on Ru and Rh loaded on La2O3 can be divided into two categories, These categories are not based on the differences in the number of x in CHx species. On Ru, x in the CHx species is equal to nearly 0, with a very small portion having x = 2. On the other hand, x is almost exclusively 0 on Rh. It seems that Rh leads to a higher rate of decomposition for methane than does Ru. (C) 2000 Academic Press.
引用
收藏
页码:115 / 121
页数:7
相关论文
共 50 条
  • [1] Methane homologation and reactivity of carbon species on supported Co catalysts
    Boskovic, G
    Smith, KJ
    CATALYSIS TODAY, 1997, 37 (01) : 25 - 32
  • [2] Catalytic Reaction of Carbon Dioxide with Methane on Supported Noble Metal Catalysts
    Erdohelyi, Andras
    CATALYSTS, 2021, 11 (02) : 1 - 30
  • [3] Methane oxidation over metal oxides supported noble metal catalysts
    Uchida, H
    Takashima, F
    Imaseki, Y
    SCIENCE AND TECHNOLOGY IN CATALYSIS 1994, 1995, 92 : 383 - 386
  • [4] TPSR studies of the activation of methane on supported noble metal catalysts
    Yan, ZF
    Song, LH
    Xue, JZ
    Shen, SK
    CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 1996, 12 (03): : 291 - 295
  • [5] STUDIES OF THE MOBILITY OF SURFACE CARBON FORMED BY THE DECOMPOSITION OF METHANE ON SUPPORTED TRANSITION METAL CATALYSTS
    YAN Zi-Feng(Department of Chemical Engineering
    Journal of Natural Gas Chemistry , 1996, (01) : 51 - 58
  • [6] Methane Combustion over the Porous Oxides and Supported Noble Metal Catalysts
    Lin, Hongxia
    Liu, Yuxi
    Deng, Jiguang
    Jing, Lin
    Dai, Hongxing
    CATALYSTS, 2023, 13 (02)
  • [7] Plasma catalytic oxidation of methane on alumina-supported noble metal catalysts
    Da Costa, Patrick
    Marques, Rui
    Da Costa, Stephanie
    APPLIED CATALYSIS B-ENVIRONMENTAL, 2008, 84 (1-2) : 214 - 222
  • [8] METHANE OXIDATION OVER ALUMINA-SUPPORTED NOBLE-METAL CATALYSTS
    OH, SH
    MITCHELL, PJ
    SIEWERT, RM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1991, 202 : 185 - COLL
  • [9] Noble metal catalysts for methane removal
    Janbey, A
    Clark, W
    Noordally, E
    Grimes, S
    Tahir, S
    CHEMOSPHERE, 2003, 52 (06) : 1041 - 1046
  • [10] Syngas Production by Methane Reforming with Carbon Dioxide on Noble Metal Catalysts
    M.Rezaei
    S.M.Alavi
    S.Sahebdelfar
    Zi-Feng Yan
    Journal of Natural Gas Chemistry, 2006, (04) : 327 - 334