Transition Metal (Fe2O3, Co3O4 and NiO)-Promoted CuO-Based α-MnO2 Nanowire Catalysts for Low-Temperature CO Oxidation

As a toxic pollutant, carbon monoxide (CO) usually causes harmful effects on human health. Therefore, the thermally catalytic oxidation of CO has received extensive attention in recent years. The CuO-based catalysts have been widely investigated due to their availability. In this study, a series of transition metal oxides (Fe2O3, Co3O4 and NiO) promoted CuO-based catalysts supported on the a-MnO2 nanowire catalysts were prepared by the deposition precipitation method for catalytic CO oxidation reactions. The effects of the loaded transition metal type, the loading amount, and the calcination temperature on the catalytic performances were systematically investigated. Further catalyst characterization showed that the CuO/a-MnO2 catalyst modified with 3 wt% Co3O4 and calcined at 400 degrees C performed the highest CO catalytic activity (T-90 = 75 degrees C) among the investigated catalysts. It was supposed that the loading of the Co3O4 dopant not only increased the content of oxygen vacancies in the catalyst but also increased the specific surface area and pore volume of the CuO/a-MnO2 nanowire catalyst, which would further enhance the catalytic activity. The CuO/a-MnO2 catalyst modified with 3 wt% NiO and calcined at 400 degrees C exhibited the highest surface adsorbed oxygen content and the best normalized reaction rate, but the specific surface area limited its activity. Therefore, the appropriate loading of the Co3O4 modifier could greatly enhance the activity of CuO/a-MnO2. This research could provide a reference method for constructing efficient low-temperature CO oxidation catalysts.

Automated summary

In this study, a series of transition metal oxides (Fe2O3, Co3O4, and NiO) promoted CuO/α-MnO2 nanowire catalysts were prepared. The CuO/α-MnO2 catalyst modified with 3 wt% Co3O4 and calcined at 400 degrees C exhibited the highest CO catalytic activity. This research provides a reference method for constructing efficient low-temperature CO oxidation catalysts.