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dc.contributor.author | Sánchez-Valente, Jaime | es_ES |
dc.contributor.author | Maya-Flores, E. | es_ES |
dc.contributor.author | Armendariz-Herrera, H. | es_ES |
dc.contributor.author | Quintana-Solorzano, R. | es_ES |
dc.contributor.author | López Nieto, José Manuel | es_ES |
dc.date.accessioned | 2020-07-08T03:32:41Z | |
dc.date.available | 2020-07-08T03:32:41Z | |
dc.date.issued | 2018-06-21 | es_ES |
dc.identifier.issn | 2044-4753 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/147640 | |
dc.description.abstract | [EN] Synthesized via the slurry method and activated at high temperature (873 K), MoVTeNb multimetallic mixed oxides are applied to catalyze the oxidative dehydrogenation of ethane to ethylene (ODHE). Mixed oxides typically contain M1 and M2 crystalline phases, the relative contribution of these phases and the respective catalytic behaviour being notably influenced by the preparation conditions of the metallic aqueous solution precursor, given the complexity of the chemical interactions of metal species in solution. Thus, detailed in situ UV-vis and Raman studies of the chemical species formed in solution during each step of the synthetic procedure are presented herein. The main role of vanadium is to form decavanadate ions, which interact with Mo species to generate an Anderson-type structure. When niobium oxalate solution is added into the MoVTe solution, a yellow-coloured gel is immediately formed due to a common ion effect. When liquid and gel phases are separated, the M1 crystalline phase is produced solely from the gel phase. Attention is also devoted to the influence and role of each metal cation (Mo, V, Te and Nb) on the formation of the active M1 crystalline phase and the catalytic behaviour in the ODHE. The catalyst constituted mostly of M1 crystalline phase is able to convert 45% of the fed ethane, with a selectivity to ethylene of around 90%. | es_ES |
dc.description.sponsorship | This work was financially supported by the Instituto Mexicano del Petroleo (IMP) Project D.61010. EMF thanks CONACyT Mexico and IMP. JMLN thanks DGICYT in Spain (Project CTQ2015-68951-C3-1-R). | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | The Royal Society of Chemistry | es_ES |
dc.relation.ispartof | Catalysis Science & Technology | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Ethane ODH | es_ES |
dc.subject | Synthesis of Mo-V-Te-Nb-O | es_ES |
dc.subject | Mixed oxide catalysts | es_ES |
dc.title | Metal solution precursors: their role during the synthesis of MoVTeNb mixed oxide catalysts | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1039/c8cy00750k | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/IMP//D.61010/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//CTQ2015-68951-C3-1-R/ES/TRATAMIENTOS CATALITICOS AVANZADOS PARA LA VALORIZACION DE LA BIOMASA Y LA ELIMINACION DE RESIDUOS ASOCIADOS/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.description.bibliographicCitation | Sánchez-Valente, J.; Maya-Flores, E.; Armendariz-Herrera, H.; Quintana-Solorzano, R.; López Nieto, JM. (2018). Metal solution precursors: their role during the synthesis of MoVTeNb mixed oxide catalysts. Catalysis Science & Technology. 8(12):3123-3132. https://doi.org/10.1039/c8cy00750k | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1039/c8cy00750k | es_ES |
dc.description.upvformatpinicio | 3123 | es_ES |
dc.description.upvformatpfin | 3132 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 8 | es_ES |
dc.description.issue | 12 | es_ES |
dc.relation.pasarela | S\383057 | es_ES |
dc.contributor.funder | Instituto Mexicano del Petróleo | es_ES |
dc.contributor.funder | Ministerio de Economía y Competitividad | es_ES |
dc.contributor.funder | Consejo Nacional de Ciencia y Tecnología, México | es_ES |
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