462966 Mixed-Oxide Based Redox Catalysts for Hydrocarbon Oxidation, Water-Splitting, and CO2 Utilization

Tuesday, November 15, 2016: 5:30 PM
Golden Gate (Hotel Nikko San Francisco)
Fanxing Li, Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC

Using transition metal oxides as the reaction intermediate, the chemical looping strategy seeks to intensify fossil fuel conversion processes via a cyclic redox scheme. In such a process, carbonaceous molecules are oxidized by active lattice oxygen (O2-) in the transition metal oxide, which functions as an oxygen carrier, a.k.a. redox catalyst. In a subsequent step, the O2- deprived oxygen carrier is replenished by a gaseous oxidant. Although conventional chemical looping processes seeks to fully oxidize fossil fuels for carbon capture, tailored redox catalysts can be applied for a variety of applications including selective oxidation, water-splitting, and CO2 reduction.

The present study exemplifies novel applications of iron and manganese containing mixed oxides for methane partial oxidation, oxidative dehydrogenation (ODH) of ethane, water-splitting, and CO2 reduction. A number of redox catalysts composed of iron and/or manganese oxides are synthesized and characterized. Rational strategies to improve the redox activity, product selectivity, and/or water-splitting and CO2 reduction conversions are investigated through the assistance of spectroscopy and ab-initio calculation tools. Compared to traditional heterogeneous catalysts, the redox catalysts in the current study show the potential to be more selective. They also possess excellent redox stability. Close to 100% water and CO2 reduction efficiencies are shown to be achievable through rational selection of mixed metal oxide based redox catalysts.

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