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dc.contributor.authorIglesias Vázquez, Sergio
dc.contributor.authorValecillos Díaz, José del Rosario
dc.contributor.authorRemiro Eguskiza, Aingeru
dc.contributor.authorBilbao Elorriaga, Javier
dc.contributor.authorGayubo Cazorla, Ana Guadalupe
dc.date.accessioned2022-05-30T10:17:47Z
dc.date.available2022-05-30T10:17:47Z
dc.date.issued2022-05-17
dc.identifier.citationCatalysts 12(5) : (2022) // Article ID 550es_ES
dc.identifier.issn2073-4344
dc.identifier.urihttp://hdl.handle.net/10810/56788
dc.description.abstractThe catalyst regeneration is still a challenge to make the ethanol steam reforming (ESR) process feasible for sustainable H2 production. NiAl2O4 spinel derived catalysts are highly active and selective for ESR, but they require avoiding irreversible deactivation to ensure their regeneration. Their stability depends on the catalyst structure, and herein we report different Ni/Al2O3-NiAl2O4 catalysts obtained upon reduction of a NiAl2O4 spinel at 700, 750, or 850 °C. The catalysts were tested in ESR reaction-regeneration cycles, with reaction at 600 °C and regeneration by coke combustion at 850 °C followed by reduction at the corresponding temperature. The fresh, spent, and regenerated catalysts were characterized using X-ray diffraction, N2 physisorption, temperature programmed reduction and oxidation, and scanning electron microscopy. The irreversible deactivation is due to Ni volatilization and catalyst particle fragmentation. These phenomena are prompted by a high filamentous carbon deposition favored by the Al2O3 content in the catalyst. The reduction in the 700–750 °C range is optimum for controlling the Al2O3 content, increasing the NiAl2O4/Al2O3 ratio in the resulting catalyst. These catalysts show a period of partial reversible deactivation by coke with a change in the H2 formation mechanism reaching a pseudo-stable state with a H2 yield of 40% and a reproducible performance in successive reaction-regeneration cycles.es_ES
dc.description.sponsorshipThis research was funded by the Ministry of Science and Innovation of the Spanish Government (grant RTI2018-100771-B-I00 and PhD grant BES-2019-090943 for S.I.-V. funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”); the European Commission (HORIZON H2020-MSCA RISE 2018. Contract No. 823745); the Department of Education, Universities and Investigation of the Basque Government, grant number IT1645-22.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/RTI2018-100771-B-I00es_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/BES-2019-090943es_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/823745es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjecthydrogenes_ES
dc.subjectethanol steam reforming (ESR)es_ES
dc.subjectNi catalystes_ES
dc.subjectNiAl2O4 spineles_ES
dc.subjectcatalyst deactivationes_ES
dc.subjectcokees_ES
dc.subjectcatalyst regenerationes_ES
dc.subjectreduction temperaturees_ES
dc.titleStability of a NiAl2O4 Derived Catalyst in the Ethanol Steam Reforming in Reaction-Regeneration Cycles: Effect of Reduction Temperaturees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2022-05-27T13:36:53Z
dc.rights.holder2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2073-4344/12/5/550/htmes_ES
dc.identifier.doi10.3390/catal12050550
dc.contributor.funderEuropean Commission
dc.departamentoesIngeniería química
dc.departamentoeuIngeniaritza kimikoa


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2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).