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dc.contributor.authorBrussino, Paula
dc.contributor.authorBortolozzi, Juan Pablo
dc.contributor.authorSanz Iturralde, Oihane ORCID
dc.contributor.authorMontes Ramírez, Mario ORCID
dc.contributor.authorUlla, María Alicia
dc.contributor.authorDavid Banús, Ezequiel
dc.date.accessioned2019-03-06T13:53:55Z
dc.date.available2019-03-06T13:53:55Z
dc.date.issued2018-07
dc.identifier.citationCatalysts 8(7) : (2018) // Article ID 291es_ES
dc.identifier.issn2073-4344
dc.identifier.urihttp://hdl.handle.net/10810/31892
dc.description.abstractThis paper investigates the oxidative dehydrogenation of ethane to produce ethylene at low temperatures (500 degrees C) in metallic structured substrates. To check this point, the FeCrAlloy (R) monoliths with different channel sizes (289-2360 cpsi) were prepared. The monoliths were coated with a Ni/Al2O3 catalyst (by washcoating of alumina and the latter nickel impregnation) and characterized by Scanning Electron Microscopy and Energy-Dispersive X-ray analysis (SEM-EDX), Temperature-Programmed Reduction (TPR), X-ray Diffraction (XRD) and X-ray Photoelectron Spectroscopy (XPS). The catalytic results showed that all monoliths coated with similar to 300 mg of catalyst presented similar ethane conversion (15%) at 450 degrees C. However, the lowest selectivity to ethylene was found for the monolith with the lower channel size and the higher geometric surface area, where a heterogeneous catalyst layer with Ni enriched islands was generated. Therefore, it can be said that the selectivity to ethylene is linked to the distribution of Ni species on the support (alumina). Nevertheless, in all cases the selectivity was high (above 70%). On the other hand, the stability in reaction tests of one of the coated monoliths was done. This structured catalyst proved to be more stable under reaction conditions than the powder catalyst, with an initial slight drop in the first 8 h but after that, constant activity for the 152 h left.es_ES
dc.description.sponsorshipThe authors acknowledge the financial support received from ANPCyT, CONICET and UNL. Also, thanks are given to the Basque Government (IT1069-16) and the Spanish MINECO/FEDER (ENE2015-66975-C3-3-R and CTQ2015-73901-JIN) for the financial support.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/ENE2015-66975-C3-3-Res_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/ CTQ2015-73901-JINes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectFeCrAlloy monolithses_ES
dc.subjectNi/Al2O3es_ES
dc.subjectoxidative dehydrogenation of ethanees_ES
dc.subjectethylenees_ES
dc.subjecto mixed oxideses_ES
dc.subjectoxidative dehydrogenationes_ES
dc.subjectstructured catalystses_ES
dc.subjectceramic paperses_ES
dc.subjectnio catalystses_ES
dc.subjectethanees_ES
dc.subjectcees_ES
dc.subjectconversiones_ES
dc.subjectnio/al2o3es_ES
dc.subjectreactorses_ES
dc.titleFeCrAlloy Monoliths Coated with Ni/Al2O3 Applied to the Low-Temperature Production of Ethylenees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.mdpi.com/2073-4344/8/7/291es_ES
dc.identifier.doi10.3390/catal8070291
dc.departamentoesQuímica aplicadaes_ES
dc.departamentoeuKimika analitikoaes_ES


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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).
Except where otherwise noted, this item's license is described as This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).