Abstract
Influence of calcination temperature (400−800°C) on the structure and catalytic activity of CuOx-CoOy-CeO2 ternary mixed oxide (atomic Cu:Co:Ce ratio of 1:5:5) prepared by co-precipitation method is investigated by N2 physisorption, XRD, TPR, TEM, TG-DTA, XPS, and CO oxidation reaction. The as-synthesized CuOx-CoOy-CeO2 undergoes successive structural changes with the calcination temperature, involving the hydroxide dehydration below 400°C, enhanced interaction between Co3O4 and CeO2 at ca. 600°C, and Co3O4 decomposition to CoO at 700°C. The catalyst calcined at 600°C shows a relative enrichment of Cu+ on the surface of CuOx-CoOy-CeO2 and an enhanced interaction between Co3O4 and CeO2 along with the appearance of oxygen vacancies in CeO2, which seems to be responsible for its highest catalytic activity for CO oxidation among all the tested catalysts. The complete conversion of CO is obtained at 70°C and about 50% of CO conversion is reached at 55°C.
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