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首页> 外文期刊>Catalysis Letters >Cobalt and Copper Composite Oxides as Efficient Catalysts for Preferential Oxidation of CO in H2-Rich Stream
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Cobalt and Copper Composite Oxides as Efficient Catalysts for Preferential Oxidation of CO in H2-Rich Stream

机译:钴和铜复合氧化物作为富H2物流中CO优先氧化的高效催化剂

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A series of Co-Cu composite oxides with different Co/Cu atomic ratios were prepared by a co-precipitation method. XRD, N2 sorption, TEM, XPS, H2-TPR, CO-TPR, CO-TPD and O2-TPD were used to characterize the structure and redox properties of the composite oxides. Only spinel structure of Co3O4 phase was confirmed for the Co-Cu composite oxides with Co/Cu ratios of 4/1 and 2/1, but the particle sizes of these composite oxides decreased evidently compared with Co3O4. These composite oxides could be reduced at lower temperatures than Co3O4 by either H2 or CO. CO and O2 adsorption amounts over the composite oxides were significantly higher than those over C03O4. These results indicated a strong interaction between cobalt and copper species in the composite samples, possibly suggesting the formation of Cu_xCo_(3-x)O4 solid solution. For the preferential oxidation of CO in a H2-rich stream, the Co-Cu composite oxides (Co/Cu = 4/1-1/1) showed distinctly higher catalytic activities than both Co3O4 and CuO, and the formation of Cu_xCo_(3_x)_O4 solid solution was proposed to contribute to the high catalytic activity of the composite catalysts. The Co-Cu composite oxide was found to exhibit higher catalytic activity than several other Co3O4-based binary oxides including Co-Ce, Co-Ni, Co-Fe and Co-Zn oxides.
机译:采用共沉淀法制备了一系列不同Co / Cu原子比的Co-Cu复合氧化物。利用XRD,N2吸附,TEM,XPS,H2-TPR,CO-TPR,CO-TPD和O2-TPD表征了复合氧化物的结构和氧化还原性能。对于Co / Cu比率为4/1和2/1的Co-Cu复合氧化物,仅确认了Co3O4相的尖晶石结构,但与Co3O4相比,这些复合氧化物的粒径明显减小。这些复合氧化物可以在比Co3O4更低的温度下被H2或CO还原。在复合氧化物上的CO和O2吸附量明显高于在CO3O4上的吸附量。这些结果表明复合样品中钴和铜物质之间有很强的相互作用,可能表明形成了Cu_xCo_(3-x)O4固溶体。为了优先富集H2的气流中的CO氧化,Co-Cu复合氧化物(Co / Cu = 4 / 1-1 / 1)的催化活性明显高于Co3O4和CuO,并且形成了Cu_xCo_(3_x提出了O_4固溶体,以促进复合催化剂的高催化活性。发现Co-Cu复合氧化物比包括Co-Ce,Co-Ni,Co-Fe和Co-Zn氧化物在内的几种其他基于Co3O4的二元氧化物具有更高的催化活性。

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