Lowering the temperature at which CH(4)is converted to useful products has been long-sought in energy conversion applications. Selective conversion to syngas is additionally desirable. Generally, most of the current CH(4)activation processes operate at temperatures between 600 and 900 degrees C when non-noble metal systems are used. These temperatures can be even higher for redox processes where a gas phase-solid reaction must occur. Here we employ the endogenous-exsolution concept to create a perovskite oxide with surface and embedded metal nanoparticles able to activate methane at temperatures as low as 450 degrees C in a cyclic redox process. We achieve this by using a non-noble, Co-Ni-based system with tailored nano- and micro-structure. The materials designed and prepared in this study demonstrate long-term stability and resistance to deactivation mechanisms while still being selective when applied for chemical looping partial oxidation of methane.

Low temperature methane conversion with perovskite-supported: exo / endo-particles / Kousi, K.; Neagu, D.; Bekris, L.; Cali', E.; Kerherve, G.; Papaioannou, E. I.; Payne, D. J.; Metcalfe, I. S.. - In: JOURNAL OF MATERIALS CHEMISTRY. A. - ISSN 2050-7488. - 8:25(2020), pp. 12406-12417. [10.1039/d0ta05122e]

Low temperature methane conversion with perovskite-supported: exo / endo-particles

Cali' E.;
2020

Abstract

Lowering the temperature at which CH(4)is converted to useful products has been long-sought in energy conversion applications. Selective conversion to syngas is additionally desirable. Generally, most of the current CH(4)activation processes operate at temperatures between 600 and 900 degrees C when non-noble metal systems are used. These temperatures can be even higher for redox processes where a gas phase-solid reaction must occur. Here we employ the endogenous-exsolution concept to create a perovskite oxide with surface and embedded metal nanoparticles able to activate methane at temperatures as low as 450 degrees C in a cyclic redox process. We achieve this by using a non-noble, Co-Ni-based system with tailored nano- and micro-structure. The materials designed and prepared in this study demonstrate long-term stability and resistance to deactivation mechanisms while still being selective when applied for chemical looping partial oxidation of methane.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11583/2989713