Volume 40 Issue 08
Aug.  2012
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SHI Rui-ping, WANG Hui, ZHU Hua-qing, WU Zhi-wei, QIN Zhang-feng, FAN Wei-bin, WANG Jian-guo. Methanol selective oxidation to methyl formate on Au-Pd/SiO2 catalysts with different calcination temperatures[J]. Journal of Fuel Chemistry and Technology, 2012, (08): 985-991.
Citation: SHI Rui-ping, WANG Hui, ZHU Hua-qing, WU Zhi-wei, QIN Zhang-feng, FAN Wei-bin, WANG Jian-guo. Methanol selective oxidation to methyl formate on Au-Pd/SiO2 catalysts with different calcination temperatures[J]. Journal of Fuel Chemistry and Technology, 2012, (08): 985-991.

Methanol selective oxidation to methyl formate on Au-Pd/SiO2 catalysts with different calcination temperatures

  • Received Date: 2011-11-03
  • Rev Recd Date: 2012-02-17
  • Publish Date: 2012-08-31
  • Au-Pd/SiO2 catalysts with different calcination temperatures were prepared by sol-immobilization method; their catalytic performance in oxidation of methanol to methyl formate was investigated. Among 200~500℃, Au-Pd/SiO2 catalyst calcined at 400℃ exhibits the best catalytic activity in the topic reaction at room temperature, and 25.3% methanol conversion with 100% selectivity to methyl formate can be achieved at100℃. They were characterized by BET, XRD, UV-vis DRS, XPS, TEM and DRIFTS. Good dispersity of Au and Pd, proper particle size of Au and Pd, the formation of Au-Pd bimetallic nanoparticles, and strong interaction between Au and Pd in the Au-Pd/SiO2 catalyst are beneficial to the oxidation of methanol to methyl formate. Furthermore, a preliminary reaction mechanism of methanol oxidation to methyl formate on the Au-Pd/SiO2 catalyst is inferred and methyl formate is gained from intermediate species methoxy in this reaction mechanism.
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