Cobalt and Copper Composite Oxides as Efficient Catalysts for Preferential Oxidation of CO in H₂-Rich Stream

Abstract

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 Co₃O₄. These results indicated a strong interaction between cobalt and copper species in the composite samples, possibly suggesting the formation of Cu _x Co_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 _x Co_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.