Gold catalysts supported on ceria-modified mesoporous zirconia for low-temperature water-gas shift reaction

V. Idakiev, T. Tabakova, K. Tenchev, Z.-Y. Yuan, T.-Z. Ren, B.-L. Su

    Résultats de recherche: Contribution à un journal/une revueArticleRevue par des pairs

    Résumé

    New gold catalytic system prepared on ceriamodified mesoporous zirconia used as water-gas shift (WGS) catalyst is reported. Mesoporous zirconia was synthesized using surfactant templating method through a neutral [C (EO) -Zr(OC H ) ] assembly pathway. Ceria modifying additive was deposited on mesoporous zirconia by deposition-precipitation method. Gold-based catalysts with different gold content (1-3 wt. %) were synthesized by deposition-precipitation of gold hydroxide on mixed metal oxide support. The supports and the catalysts were characterized by powder X-ray diffraction, high-resolution transmission electron microscopy, N adsorption analysis and temperature programmed reduction. The catalytic behavior of the gold-based catalysts was evaluated in WGS reaction in a wide temperature range (140-300 °C) and at different space velocities and H O/CO ratios. The influence of gold content and particle size on the catalytic performance was investigated. The WGS activity of the new Au/ceria-modified mesoporous zirconia catalysts was compared with that of gold catalysts supported on simple oxides CeO and mesoporous ZrO , revealing significantly higher catalytic activity of Au/ceria-modified mesoporous zirconia. A high degree of synergistic interaction between ceria and mesoporous zirconia and a positive modification of structural and catalytic properties by ceria have been achieved. It is clearly revealed that the ceria-modified mesoporous zirconia is of much interest as potential support for gold-based catalyst. The Au/ceria-modified mesoporous zirconia catalytic system is found to be effective catalyst for WGS reaction.
    langue originaleAnglais
    Pages (de - à)15-20
    Nombre de pages6
    journalJournal of Porous Materials
    Volume19
    Numéro de publication1
    Les DOIs
    Etat de la publicationPublié - 1 févr. 2012

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