催化作用
化学
材料科学
化学工程
无机化学
有机化学
工程类
作者
Meng‐Fei Luo,Yijun Zhong,Xianxin Yuan,Xiaoming Zheng
标识
DOI:10.1016/s0926-860x(97)00089-6
摘要
Abstract Copper oxide supported on cerium dioxide ( CuO CeO 2 ) catalysts were prepared and used for carbon monoxide oxidation in stoichiometric carbon monoxide and oxygen. The catalysts were characterized by means of XRD, H2-TPR and CO-TPD studies. The CuO CeO 2 catalysts exhibit high catalytic activity in CO oxidation, showing markedly enhanced catalytic activities due to the combined effect of copper oxide and cerium dioxide. The activity of the CuO CeO 2 (15%) catalyst prepared by impregnation is higher than that prepared by co-precipitation. CeO2 promotes the hydrogen reduction activity of copper, so that CuO CeO 2 catalysts show a different behavior with respect to pure CuO. Two reducible copper species were observed in all CuO CeO 2 catalysts. CO-TPD experiments revealed that CuO CeO 2 catalysts can adsorb CO, while pure CuO and CeO2 cannot. Combining the results of TPR, TPD study, and the catalytic activity measurements, it is proposed that the well dispersed CuO which can adsorb CO and which is reducible at low-temperature is responsible for low-temperature CO oxidation. The bulk CuO which cannot adsorb CO and which is reducible at high-temperature contributes little to the oxidation activity.
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