CuO/cryptomelane catalyst for preferential oxidation of CO in the presence of H2: deactivation and regeneration

Please use this identifier to cite or link to this item: http://hdl.handle.net/10045/57225
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dc.contributorMateriales Carbonosos y Medio Ambientees_ES
dc.contributor.authorDavó-Quiñonero, Arantxa-
dc.contributor.authorNavlani García, Miriam-
dc.contributor.authorLozano Castelló, Dolores-
dc.contributor.authorBueno López, Agustín-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Inorgánicaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Materialeses_ES
dc.date.accessioned2016-07-26T11:10:09Z-
dc.date.available2016-07-26T11:10:09Z-
dc.date.issued2016-04-11-
dc.identifier.citationCatalysis Science & Technology. 2016, 6: 5684-5692. doi:10.1039/C6CY00329Jes_ES
dc.identifier.issn2044-4753 (Print)-
dc.identifier.issn2044-4761 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/57225-
dc.description.abstractCryptomelane and CuO/cryptomelane catalysts have been tested in the preferential oxidation of CO in the presence of H2 (CO-PROX reaction), paying special attention to deactivation and regeneration issues. Cryptomelane was stable during the CO-PROX reactions in ramp experiments until 200 °C and in a long-term isothermal experiment (10 h). Changes neither in the H2 reducibility and porosity nor in the crystalline phases detected by XRD were observed. On the contrary, CuO/cryptomelane was partially deactivated during the consecutive CO-PROX reaction cycles performed until 200 °C, and the catalytic activity was partially restored by reoxidising the catalyst at 200 °C or 400 °C, the latter temperature being more effective. In spite of the CuO/cryptomelane partial deactivation, the CO-PROX activity of this catalyst was higher than that of cryptomelane once a stable behaviour was achieved. The partial deactivation of CuO/cryptomelane was attributed to the segregation of crystalline phases (hausmannite (Mn3O4) and/or hopcalite (CuMn2O4)), with the segregation of potassium to the surface and decrease in the copper cations' reducibility. The potential contribution to deactivation of the changes in the porous texture of CuO/cryptomelane was ruled out.es_ES
dc.description.sponsorshipThe authors are thankful for the financial support from Generalitat Valenciana (Project PROMETEOII/2014/010), the Spanish Ministry of Economy and Competitiveness (Project MAT2014-61992-EXP and CTQ2015-67597-C2-2-R), the Spanish Ministry of Education, Culture and Sports (grant FPU14/01178), the Spanish Catalysis Society (SECAT TFM 2015), and the UE (FEDER funding).es_ES
dc.languageenges_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.es_ES
dc.subjectCuO/cryptomelane catalystses_ES
dc.subjectPreferential oxidationes_ES
dc.subjectCOes_ES
dc.subjectH2es_ES
dc.subject.otherQuímica Inorgánicaes_ES
dc.titleCuO/cryptomelane catalyst for preferential oxidation of CO in the presence of H2: deactivation and regenerationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1039/C6CY00329J-
dc.relation.publisherversionhttp://dx.doi.org/10.1039/C6CY00329Jes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
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