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Co/ZrO2, Co/CeO2 and MnCoCe structured catalysts for COPrOx

机译:用于COPrOx的Co / ZrO2,Co / CeO2和MnCoCe结构催化剂

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Cordierite monoliths washcoated with MnCoCe(CP), Co(I)/ZrO2 and Co(I)/CeO2 catalysts were prepared and studied for the CO preferential oxidation (COPrOx) reaction. Among them, the MnCoCe/M system presented the best CO conversion at low temperatures and the Co(I)/CeO2 -M catalyst, the best selectivities toward CO2. In the three catalysts, Co3O4 was the main Co containing compound and it was the active species for the COPrOx reaction. Nevertheless, the Co(i)/CeO2-M and MnCoCe/M solids resulted more active than Co(I)/ZrO2-M, possibly due to the better redox properties of the ceria. In the MnCoCe/M catalyst prepared by co-precipitation, the addition of Mn represented an additional positive effect. The presence of Mn promoted the re-oxidation of Co~(2+) to Co~(3+) and, consequently, the activity increased at low temperature. It is also shown that homogeneous and mechanically stable coatings on the walls of the three monolithic catalysts were obtained, which in turn yielded promising results in the COPrOx reaction.
机译:制备了用MnCoCe(CP),Co(I)/ ZrO2和Co(I)/ CeO2催化剂修补涂层的堇青石整料,并研究了CO优先氧化(COPrOx)反应。其中,MnCoCe / M系统在低温下表现出最佳的CO转化率,而Co(I)/ CeO2-M催化剂表现出对CO2的最佳选择性。在这三种催化剂中,Co3O4是主要的含Co化合物,并且是COPrOx反应的活性物种。尽管如此,Co(i)/ CeO2-M和MnCoCe / M固体比Co(I)/ ZrO2-M的活性更高,这可能是由于二氧化铈具有更好的氧化还原特性。在通过共沉淀制备的MnCoCe / M催化剂中,Mn的添加表现出附加的积极作用。 Mn的存在促进了Co〜(2+)向Co〜(3+)的再氧化,因此活性在低温下增加。还显示在三种整体式催化剂的壁上获得均匀且机械稳定的涂层,这反过来在COPrOx反应中产生了令人鼓舞的结果。

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