Deactivation mechanism of nanosized gold catalysts stored in ambient air

被引:0
|
作者
Wang Donghui [1 ]
Dong Tongxin
Shi Xicheng
Hao Zhengping
机构
[1] Chinese Peoples Liberat Army, Res Inst Chem Def, Beijing 100083, Peoples R China
[2] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
关键词
nanoparticle; gold; zinc oxide; supported catalyst; carbon monoxide oxidation; deactivation mechanism; carbonate;
D O I
暂无
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A nanosized 2.5% Au/ZnO catalyst was prepared using the coprecipitation method at low temperature. The deactivation mechanism of the catalyst stored in ambient air was investigated using scanning transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The deactivation of the catalyst was partially reversible, and two factors interrelated the deactivation. One was the agglomeration of nanosized gold particles, which caused the irreversible deactivation. The other was the accumulation of carbonates on the catalyst surface, leading to the reversible deactivation. The carbonates could be decomposed when the deactivated catalyst was calcined at high temperature.
引用
收藏
页码:148 / 152
页数:5
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共 21 条
  • [1] FTIR, UV-Vis, and HRTEM study of Au/ZrO2 catalyst:: Reduced reactivity in the CO-O2 reaction of electron-deficient gold sites present on the used samples
    Boccuzzi, F
    Cerrato, G
    Pinna, F
    Strukul, G
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (30): : 5733 - 5736
  • [2] Catalysis by gold
    Bond, GC
    Thompson, DT
    [J]. CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (3-4): : 319 - 388
  • [3] Detection of Mycobacterium tuberculosis antigens in urinary proteins of tuberculosis patients
    Choudhry, V
    Saxena, RK
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2002, 21 (01) : 1 - 5
  • [4] On the potential role of hydroxyl groups in CO oxidation over Au/Al2O3
    Costello, CK
    Yang, JH
    Law, HY
    Wang, Y
    Lin, JN
    Marks, LD
    Kung, MC
    Kung, HH
    [J]. APPLIED CATALYSIS A-GENERAL, 2003, 243 (01) : 15 - 24
  • [5] The mechanism of low-temperature CO oxidation with Au/Fe2O3 catalysts:: a combined Mossbauer, FT-IR, and TAP reactor study
    Daniells, ST
    Overweg, AR
    Makkee, M
    Moulijn, JA
    [J]. JOURNAL OF CATALYSIS, 2005, 230 (01) : 52 - 65
  • [6] Performance of Au/TiO2 catalyst under ambient conditions
    Daté, M
    Ichihashi, Y
    Yamashita, T
    Chiorino, A
    Boccuzzi, F
    Haruta, A
    [J]. CATALYSIS TODAY, 2002, 72 (1-2) : 89 - 94
  • [7] Gold as a novel catalyst in the 21st century: Preparation, working mechanism and applications
    Haruta, M
    [J]. GOLD BULLETIN, 2004, 37 (1-2) : 27 - 36
  • [8] Deactivation of Au/CeOx water gas shift catalysts
    Kim, CH
    Thompson, LT
    [J]. JOURNAL OF CATALYSIS, 2005, 230 (01) : 66 - 74
  • [9] Deactivation of nanosize gold supported on zirconia in CO oxidation
    Konova, P
    Naydenov, A
    Tabakova, T
    Mehandjiev, D
    [J]. CATALYSIS COMMUNICATIONS, 2004, 5 (09) : 537 - 542
  • [10] Active oxygen species and mechanism for low-temperature CO oxidation reaction on a TiO2-supported Au catalyst prepared from Au(PPh3)(NO3) and As-precipitated titanium hydroxide
    Liu, H
    Kozlov, AI
    Kozlova, AP
    Shido, T
    Asakura, K
    Iwasawa, Y
    [J]. JOURNAL OF CATALYSIS, 1999, 185 (02) : 252 - 264