催化作用
锰
原位
X射线光电子能谱
化学
无机化学
吸附
反应性(心理学)
化学工程
氧气
物理化学
有机化学
医学
工程类
病理
替代医学
作者
Qiulin Zhang,Jia Hu,Ping Ning,Xin Liu,Huimin Wang,Guangcheng Wei,Tengxiang Zhang
标识
DOI:10.1016/j.jtice.2019.02.011
摘要
Abstract A series of different manganese oxides supported Pd catalysts with low Pd loading of 0.3 wt.% have been synthesized and applied to CO catalytic oxidation at low-temperature. In situ DRIFTS was employed to dynamically trace CO oxidation process. It was found that the CO catalytic activity decreased in the order of Pd/OMS-2 > Pd/MnO2 > Pd/Mn2O3 >> Pd/Mn3O4. More interestingly, the Pd/OMS-2 catalyst exhibited exceptionally high activity of T99 = 16 °C, as well as higher reducibility. Furthermore, XPS and in situ DRIFTS results indicated that a substantial of lattice oxygen participated in CO oxidation, contributing to the optimal activity over Pd/OMS-2. While the low reactivity over Pd/Mn3O4 was ascribed to a small amount of lattice oxygen and the strongly adsorbed CO on Pd0.
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