Selective production of hydrogen from partial oxidation of methanol over supported silver catalysts prepared by method of redox coprecipitation

被引:31
|
作者
Mo, Liuye [2 ,3 ]
Wan, Albert H. [2 ]
Zheng, Xiaoming [3 ]
Yeh, Chuin-Tih [1 ,2 ]
机构
[1] Yuan Ze Univ, Fuel Cell Ctr, Tao Yuan 320, Taiwan
[2] Natl Tsing Hua Univ, Dept Chem, Hsinchu, Taiwan
[3] Zhejiang Univ, Inst Catalysis, Key Lab Appl Chem Zhejiang Prov, Hangzhou 310028, Peoples R China
基金
美国国家科学基金会;
关键词
Method of redox coprecipitation; Silver catalysts; Hydrogen production; Partial oxidation of methanol; DECOMPOSITION; ADSORPTION; SURFACE; CERIA; CU/ZNO/AL2O3; PERFORMANCE; OXYGEN; XPS;
D O I
10.1016/j.cattod.2009.04.002
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Supported silver catalysts showed good activity for hydrogen production from partial oxidation of methanol (POM) at a low temperature of 160 degrees C. Ag/CeO2-ZnO catalysts, prepared by the method of redox coprecipitation, displayed distinguished hydrogen selectivity (S-H2) and methanol conversion. In preparation of the catalysts, Ag+ ions were found reduced into metal clusters by Ce3+ ions. X-ray diffraction study revealed that the active silver crystallites were dispersed amorphously on the catalysts. Thermal characterization of temperature programmed hydrogen reduction and temperature programmed hydrogen desorption further suggested that CeO2 and ZnO played different roles in the high S-H2 over Ag/CeO2-ZnO. Promoter CeO2 served as a spillover sink to collect hydrogen dissociated on silver crystallites while ZnO acted as a porthole for a fast desorption of hydrogen from the catalyst. These two oxides corporately raised the high S-H2 over Ag/CeO2-ZnO catalysts. (C) 2009 Published by Elsevier B.V.
引用
收藏
页码:124 / 129
页数:6
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