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dc.contributor.authorSantamaría Moreno, Laura ORCID
dc.contributor.authorArtetxe Uria, Maite
dc.contributor.authorLópez Zabalbeitia, Gartzen ORCID
dc.contributor.authorCortázar Dueñas, María ORCID
dc.contributor.authorAmutio Izaguirre, Maider
dc.contributor.authorBilbao Elorriaga, Javier
dc.contributor.authorOlazar Aurrecoechea, Martin ORCID
dc.date.accessioned2020-10-02T16:31:16Z
dc.date.available2020-10-02T16:31:16Z
dc.date.issued2019-10-25
dc.identifier.citationFuel Processing Technology 198 : (2020) // art. id: 106223 // https://doi.org/10.1016/j.fuproc.2019.106223es_ES
dc.identifier.issn0378-3820
dc.identifier.urihttp://hdl.handle.net/10810/46373
dc.description.abstractA Ni/Al2O3 catalyst has been modified incorporating CeO2 and MgO promoters in order to improve its performance in the steam reforming of biomass pyrolysis volatiles. Ni/Al2O3, Ni/CeO2-Al2O3 and Ni/MgO-Al2O3 catalysts have been prepared and fresh and deactivated catalysts have been characterized by N2 adsorption/ desorption, X-ray Fluorescence (XRF), Temperature Programmed Reduction (TPR), X-ray powder diffraction (XRD), Temperature Programmed Oxidation (TPO), Transmission Electron Microscopy (TEM) and a technique based on Fourier Transform Infrared Spectroscopy-Temperature Programmed Oxidation (FTIR-TPO). The results obtained revealed a similar initial activity for the three catalysts tested (conversion higher than 98%), whereas stability has been greatly improved by incorporating CeO2 as promoter, as it enhances the gasification of coke precursors. However, Ni/MgO-Al2O3 catalyst is slightly less stable than Ni/Al2O3, presumably as a result of its lower reducibility due to the formation of MgAl2O4 spinel phase. Catalysts deactivation has been associated with coke deposition, although sintering phenomenon became also evident when the Ni/CeO2-Al2O3 catalyst was tested. The coke deposited on the catalysts does not present any specific morphology, which is evidence of its amorphous structure in the three catalysts studied.es_ES
dc.description.sponsorshipThis work was carried out with financial support from the Ministry of Economy and Competitiveness of the Spanish Government (CTQ2016-75535-R (AEI/FEDER, UE) and CTQ-2015-69436-R (MINECO/FEDER, UE)), Ministry of Science, Innovation and Universities of the Spanish Government (RTI2018-101678-B-I00 (MCIU/AEI/FEDER, UE)), the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 823745, and the Basque Government (IT1218-19).es_ES
dc.language.isoenges_ES
dc.publisherElsevier B.V.es_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/823745es_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2016-75535-Res_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2015-69436-Res_ES
dc.relationinfo:eu-repo/grantAgreement/MCIU/RTI2018-101678-B-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjecthydrogenes_ES
dc.subjectsteam reforminges_ES
dc.subjectbiomasses_ES
dc.subjectnickel catalystes_ES
dc.subjectpromoterses_ES
dc.subjectceriaes_ES
dc.titleEffect of CeO2 and MgO promoters on the performance of a Ni/Al2O3 catalyst in the steam reforming of biomass pyrolysis volatileses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 licensees_ES
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0378382019308562es_ES
dc.identifier.doi10.1016/j.fuproc.2019.106223
dc.contributor.funderEuropean Commission
dc.departamentoesIngeniería químicaes_ES
dc.departamentoeuIngeniaritza kimikoaes_ES


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© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license
Except where otherwise noted, this item's license is described as © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license