Citation: ZHANG Yan-jie, CHEN Chong-qi, ZHAN Ying-ying, LIN Qi, LOU Ben-yong, ZHENG Guo-cai, ZHENG Qi. Highly active Y-promoted CuO/ZrO2 catalysts for the production of hydrogen through water-gas shift reaction[J]. Journal of Fuel Chemistry and Technology, ;2017, 45(9): 1137-1145. shu

Highly active Y-promoted CuO/ZrO2 catalysts for the production of hydrogen through water-gas shift reaction

  • Corresponding author: ZHANG Yan-jie, yanjiezhang@mju.edu.cn ZHAN Ying-ying, jennyzan@fzu.edu.cn
  • Received Date: 18 May 2017
    Revised Date: 29 June 2017

    Fund Project: Natural Science Foundation of Fujian Province 2017J01584Natural Science Foundation of Fujian Province 2017J05025the National Natural Science Foundation of China 21503105JK Project of the Education Department of Fujian Province JK2015038The project was supported by the National Natural Science Foundation of China (21503105), Natural Science Foundation of Fujian Province (2017J05025, 2017J01584), JK Project of the Education Department of Fujian Province (JK2015038), JA Project of the Education Department of Fujian Province (JA15419) and the plan of college outstanding young research talents in Fujian Province(2016)JA Project of the Education Department of Fujian Province JA15419

Figures(6)

  • ZrO2 doped with various concentrations of yttrium(0-5%) was prepared by a hydrothermal homogeneous co-precipitation method and CuO was then deposited on ZrO2 by a deposition-precipitation method to get the yttrium promoted CuO/ZrO2 catalyst; its performance in the water-gas shift reaction for producing hydrogen was then investigated. The results indicate that the catalytic activity of CuO/ZrO2 can be effectively improved by yttrium modification; over the yttrium promoted CuO/ZrO2 catalyst with an yttrium concentration of 2%, the CO conversion reaches 91.4% at 270℃, much higher than those over the conventional CuO/ZnO and CuO/CeO2 catalysts. The XRD, N2-physisorption, N2O titration, SEM and CO-TPR characterization results reveal that Y3+ is successfully incorporated into the lattice of ZrO2, which has a great influence on the structure and reducibility of the CuO/ZrO2 catalysts. Y3+ doping into ZrO2 introduces oxygen vacancies, improving the dispersion of CuO and increasing the proportion of catalytically active Cu-[O]-Zr species. In addition, the introduction of yttrium improves the monodispersity and modifies the texture properties of the CuO/ZrO2 catalysts. As a result, the superior activity of 2% yttrium promoted CuO/ZrO2 catalyst is probably attributed to the abundance of Cu-[O]-Zr species, high reducibility of Cu-[O]-Zr species and surface hydroxyl groups, high monodispersity and proper textural properties.
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