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Structure-activity relationship in water-gas shift reaction over gold catalysts supported on Y-doped ceria

Journal of Rare Earths 2019年第4期37卷 383-392页

作者： Tatyana Tabakova Lyuba Ilieva Ivan Ivanov Maela Manzoli rodolfo zanella Petya Petrova Zbigniew Kaszkur Institute of Catalysis Bulgarian Academy of Sciences Department of Drug Science and Technology & Centre for Nanostructured Interfaces and Surfaces University of Turin Centro de Ciencias Aplicadas y Desarrollo Tecnologico Universidad Nacional Autonoma de Mexico Institute of Physical Chemistry PAS

The utilization of pure hydrogen as an energy source in fuel cells gave rise to renewed interest in developing active and stable water-gas shift catalysts. Gold catalysts have proven to be very efficient for water-gas shift reaction at low temperature. The aim of the present study was to investigate the effect of:(i) different preparation methods(impregnation and coprecipitation) to obtain a modified ceria support,and(ii) the amount of Y_2 O_3(1.0 wt%, 2.5 wt%, 5.0 wt% and 7.5 wt%) as dopant on the water-gas shift activity of Au/CeO_2 catalysts. An extended characterization by means of S_(BET), XRD, HRTEM/HAADF, FTIR,H_2-TPR and CO-TPR measurements in combination with careful evaluation of the catalyst behavior allowed to shed light on the parameters governing the water-gas shift activity. The catalysts show very high activity(>90% CO conversion) in the temperature range 180-220 ℃,with a slightly better performance of the gold catalysts on supports prepared by impregnation. The decreased activity with increasing Y_2 O_3 concentration is related to the hindering of oxygen mobility due to ordering of surface oxygen vacancies in vicinity of segregated Y^(3+). The effect of catalyst pre-treatments and the stability of the best performing samples were examined as well.

关键词： Gold catalyst Water gas shift reaction Doped ceria Yttrium Hydrogen production Rare earths

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Gold-iridium catalysts for the hydrogenation of biomass derived products

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Chinese Journal of Catalysis 2016年第10期37卷 1771-1775页

作者： Lorenzo Landenna Alberto Villa rodolfo zanella Claudio Evangelisti Laura Prati 米兰大学化学系墨西哥国立自治大学科学应用与技术开发中心意大利国家研究委员会分子科学技术研究所

Au-Ir and Au-Ru on TiOz catalysts prepared by sequential deposition-precipitation technique were compared with the corresponding monometallics in the hydrogenation of levulinic acid to y-valero]actone. Interestingly the addition of Ao to Ir/TiO2 showed a detrimental effect on the activity of Ir monometallic catalyst whereas a positive synergistic effect was shown in the case of Ru. Both catalysts were reduced under H2 to increase the M0-Au0 interaction, From previous DFT calculations and catalytic test, we addressed the lower activity of Au-lr/TiO2 than that of Ir/TiO2 to the interference of Au into the redox mechanism of lr atoms.

关键词： Levulinic acid hydrogenationGold-irdium catalystGold-ruthenium catalysty-ValerolactoneSynergistic effect

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