Evolution of the optimal catalytic systems for the oxidative dehydrogenation of ethane: The role of adsorption in the catalytic performance
[EN] Three samples that correspond to the evolution of optimal catalytic systems for the oxidative dehydrogenation of ethane have been synthesized and compared in terms of catalytic behavior and adsorption properties: (i) vanadium oxide supported on alumina, (ii) Sn-promoted NiO, and (iii) multicomp...
| Authors: | , , , , , , |
|---|---|
| Format: | article |
| Publication Date: | 2022 |
| Country: | España |
| Institution: | Universitat Politècnica de València (UPV) |
| Repository: | RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia |
| Language: | English |
| OAI Identifier: | oai:riunet.upv.es:10251/194946 |
| Online Access: | https://riunet.upv.es/handle/10251/194946 |
| Access Level: | Open access |
| Keyword: | ODH ethane Ethylene FT-IR adsorbed ethylene Microcalorimetry MoVTeNb Promoted NiO 12.- Garantizar las pautas de consumo y de producción sostenibles |
| Summary: | [EN] Three samples that correspond to the evolution of optimal catalytic systems for the oxidative dehydrogenation of ethane have been synthesized and compared in terms of catalytic behavior and adsorption properties: (i) vanadium oxide supported on alumina, (ii) Sn-promoted NiO, and (iii) multicomponent MoVTeNbO with the M1 structure. The main difference in catalytic performance lies in the extent of the overoxidation of the ethylene formed, following the order VOx/Al2O3 > NiSnOx > MoVTeNb-M1. Accordingly, the selectivity to ethylene at medium and high ethane conversion follows the order MoVTeNb-M1 > NiSnOx > VOx/Al2O3. These results are confirmed by the relative reaction rates observed for the oxidation of ethane and the oxidation of ethylene. Microcalorimetry studies indicate that the heat of adsorption of both ethane and ethylene is the highest in the most selective MoVTeNb-M1 sample. Thus, the low olefin decomposition in the MoVTeNb-M1 catalyst is not due to weaker adsorption of ethylene but to the reduced ability of its active sites to activate ethylene. The same conclusion regarding the MoVTeNb-M1 catalyst can be drawn by FT-IR of adsorbed ethylene. On the other hand, NiSnOx active sites present a high overoxidation ability, as demonstrated by the notorious formation of oxygenated species, precursors of COx. However, the ethylene decomposition is rather mild because of the existence of many free Lewis sites not involved in the overoxidation reaction. In contrast, in the case of the VOx/Al2O3 catalyst, almost all active sites are involved in the oxidation path, so that the olefins decompose readily. |
|---|