Volume 37 Issue 05
Oct.  2009
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WU Rui-Fang, Zhang-Yin, Wang-Yong-Zhao, Gao-Chun-Guang, Diao-Yong-Xiang. Effect of ZrO2 promoter on the catalytic activity for CO methanation and its adsorption performance of the Ni/SiO2 catalyst[J]. Journal of Fuel Chemistry and Technology, 2009, 37(05): 578-582.
Citation: WU Rui-Fang, Zhang-Yin, Wang-Yong-Zhao, Gao-Chun-Guang, Diao-Yong-Xiang. Effect of ZrO2 promoter on the catalytic activity for CO methanation and its adsorption performance of the Ni/SiO2 catalyst[J]. Journal of Fuel Chemistry and Technology, 2009, 37(05): 578-582.

Effect of ZrO2 promoter on the catalytic activity for CO methanation and its adsorption performance of the Ni/SiO2 catalyst

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  • Received Date: 2009-01-06
  • Rev Recd Date: 2009-04-20
  • Publish Date: 2009-10-31
  • The catalytic activities for CO methanation and adsorption performances of the Ni/SiO2 and Ni/ZrO2-SiO2 catalysts were investigated by a continuous flowing microreactor apparatus and in-situ diffuse reflectance fourier transform infrared spectroscopy. The results showed that CO was completely transformed at 200℃ under the reaction conditions: CO 1%、GHSV 5000h-1 and an atmosphere pressure over the Ni/ZrO2-SiO2 catalyst, while under the same reaction conditions the CO conversion was only 35% and CO was not completely transformed until 270℃ over the Ni/SiO2 catalyst, which suggested the catalytic activity of the Ni/ZrO2SiO2 catalyst increased with the addition of ZrO2 promoter. Meanwhile, the addition of ZrO2 promoter enhanced the adsorption capacity of the Ni/ZrO2-SiO2 catalyst for CO, and that in the presence of H2 a larger amount of bridged carbonyl hydride formed over the Ni/ZrO2-SiO2 catalyst at lower temperature, resulting in the increase of its catalytic activity. In CO methanation reaction, the breaking of C—O bond over those catalysts was via multi-hydrogen carbonyl hydride rather than via direct breaking.
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