Au-TiO2 catalysts on carbon nanotibres prepared by deposition-precipitation and from colloid solutions

被引:30
作者
Hammer, Nina
Kvande, Ingvar
Xu, Xin
Gunnarsson, Vidar
Totdal, Bard
Chen, De
Ronning, Magnus [1 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway
[2] Beijing Inst Petrochem Technol, Beijing 102617, Peoples R China
[3] Norwegian Univ Sci & Technol, Dept Phys, N-7491 Trondheim, Norway
关键词
Au catalyst; TiO2; carbon nanofibres; water-gas shift reaction; deposition-precipitation; Au colloids;
D O I
10.1016/j.cattod.2007.03.001
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An catalysts have been prepared (i) on TiO2, (ii) on carbon nanofibres (CNF) and (iii) on TiO2 deposited onto CNF. Catalysts prepared from deposition-precipitation (DP) and from colloid solutions have been characterised using XRD, TEM, TGA and XAS and tested in the water-gas shift (WGS) reaction. DP yields large An particles (> 50 nm) on CNF-containing supports. High An dispersion on carbon nanofibres requires preparation via other methods such as colloid formation. An particle growth is more pronounced during the synthesis steps than during thermal treatments. This increase is not observed for the Au particles on TiO2 but only when CNF is present, indicating that the surface properties of TiO2 are altered by the CNF TiO2 XANES analyses show that distortions in the lattice symmetry of TiO2 are introduced when the oxide is deposited on CNE The distortion of the TiO2 structure by the CNF may also introduce changes that promote the turnover frequencies. The WGS activity significantly improves when titania is present. This shows that coexistence of An and TiO2 is needed to obtain high catalytic activity in the WGS reaction, indicating that the active sites are either on the Au-TiO2 interface or that the reaction follows a bifunctional mechanism. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 256
页数:12
相关论文
共 62 条
  • [1] Low-temperature water-gas shift reaction over Au/alpha-Fe2O3
    Andreeva, D
    Idakiev, V
    Tabakova, T
    Andreev, A
    [J]. JOURNAL OF CATALYSIS, 1996, 158 (01) : 354 - 355
  • [2] Carbons as supports for industrial precious metal catalysts
    Auer, E
    Freund, A
    Pietsch, J
    Tacke, T
    [J]. APPLIED CATALYSIS A-GENERAL, 1998, 173 (02) : 259 - 271
  • [3] Gold, silver and copper catalysts supported on TiO2 for pure hydrogen production
    Boccuzzi, F
    Chiorino, A
    Manzoli, M
    Andreeva, D
    Tabakova, T
    Ilieva, L
    Iadakiev, V
    [J]. CATALYSIS TODAY, 2002, 75 (1-4) : 169 - 175
  • [4] A kinetic and DRIFTS study of low-temperature carbon monoxide oxidation over Au-TiO2 catalysts
    Bollinger, MA
    Vannice, MA
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 1996, 8 (04) : 417 - 443
  • [5] Thermogravimetric analysis of the oxidation of multiwalled carbon nanotubes: Evidence for the role of defect sites in carbon nanotube chemistry
    Bom, D
    Andrews, R
    Jacques, D
    Anthony, J
    Chen, BL
    Meier, MS
    Selegue, JP
    [J]. NANO LETTERS, 2002, 2 (06) : 615 - 619
  • [6] Catalysis by gold
    Bond, GC
    Thompson, DT
    [J]. CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (3-4): : 319 - 388
  • [7] ELECTRON-ENERGY LOSS AND X-RAY ABSORPTION-SPECTROSCOPY OF RUTILE AND ANATASE - A TEST OF STRUCTURAL SENSITIVITY
    BRYDSON, R
    SAUER, H
    ENGEL, W
    THOMAS, JM
    ZEITLER, E
    KOSUGI, N
    KURODA, H
    [J]. JOURNAL OF PHYSICS-CONDENSED MATTER, 1989, 1 (04) : 797 - 812
  • [8] Highly dispersed gold on activated carbon fibers for low-temperature CO oxidation
    Bulushev, DA
    Yuranov, I
    Suvorova, EI
    Buffat, PA
    Kiwi-Minsker, L
    [J]. JOURNAL OF CATALYSIS, 2004, 224 (01) : 8 - 17
  • [9] Hydrogen chemisorption on Al2O3-supported gold catalysts
    Bus, E
    Miller, JT
    van Bokhoven, JA
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (30) : 14581 - 14587
  • [10] Cameron D.S., 1990, CATAL TODAY, V7, P113, DOI DOI 10.1016/0920-5861(90)85012-D