CO2 Reduction over Mo2C-Based Catalysts
[EN] Four Mo-based catalysts were prepared via three different synthesis techniques supported on SiO2 and/or SBA-15. By means of complementary in situ characterization techniques, the carburization process and the final characteristics of these catalysts were investigated. Additionally, the four cat...
| Autores: | , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2021 |
| País: | España |
| Institución: | Universitat Politècnica de València (UPV) |
| Repositorio: | RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia |
| Idioma: | inglés |
| OAI Identifier: | oai:riunet.upv.es:10251/183199 |
| Acceso en línea: | https://riunet.upv.es/handle/10251/183199 |
| Access Level: | acceso abierto |
| Palabra clave: | Carbon dioxide Hydrogen Reverse water-gas shift Molybdenum carbide In situ XRD In situ Raman spectroscopy In situ XAS |
| Sumario: | [EN] Four Mo-based catalysts were prepared via three different synthesis techniques supported on SiO2 and/or SBA-15. By means of complementary in situ characterization techniques, the carburization process and the final characteristics of these catalysts were investigated. Additionally, the four catalysts were evaluated for the activation of CO2 in the absence and presence of H-2 (reverse water-gas shift, RWGS). The results suggest that CO2 reacts via a dissociation on the carbide surface, forming adsorbed oxygen surface species. Severe oxidation of the carbide into its oxidic phases (MoO2 or MoO3) only occurs at temperatures above 850 K in the presence of CO2. O-2 dissociates on the carbide surface when introduced at low concentrations (1 vol %) at room temperature, but when exposed to higher concentrations, a strong exothermic bulk re-oxidation reaction occurs, forming MoO2. All four catalysts show high RWGS activity in terms of CO2 conversions with a minimum CO selectivity of 98% without any signs of bulk catalyst oxidation. Although minimal, the observed deactivation is suggested to be primarily due to phase changes between Mo2C allotropes (beta-phase, oxycarbide, and eta-phase) and/or sintering of the active phase. |
|---|