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dc.contributor.authorArregi Joaristi, Aitor
dc.contributor.authorLópez Zabalbeitia, Gartzen ORCID
dc.contributor.authorAmutio Izaguirre, Maider
dc.contributor.authorArtetxe Uria, Maite
dc.contributor.authorBarbarias Barainka, Itsaso
dc.contributor.authorBilbao Elorriaga, Javier
dc.contributor.authorOlazar Aurrecoechea, Martin ORCID
dc.date.accessioned2024-02-09T13:59:17Z
dc.date.available2024-02-09T13:59:17Z
dc.date.issued2017-12-09
dc.identifier.citationFuel 216 : 233-244 (2018)
dc.identifier.issn0016-2361
dc.identifier.urihttp://hdl.handle.net/10810/65935
dc.description.abstractThe effect of reforming conditions (temperature, space time and steam/biomass ratio (S/B)) has been studied in the continuous biomass pyrolysis and in-line catalytic steam reforming process in order to establish suitable conditions for attenuating the deactivation of a commercial Ni catalyst by coke deposition. The experiments have been performed in a conical spouted bed and a fluidized bed reactor for the pyrolysis and reforming steps, respectively. Biomass fast pyrolysis was performed at 500 ºC and the reforming operating conditions studied are as follows: 550-700 ºC; space-time, 10-30 gcatalyst min gvolatiles-1, and; S/B ratio, 2-5. The coke deposited on the catalyst has been analyzed by temperature programmed oxidation (TPO), and two types of coke have been identified, i.e., the coke deposited on the Ni active sites and the one separated from these sites, without filamentous coke being observed by transmission electron microscopy (TEM). Coke deposition has been related to the decomposition of the oxygenates derived from biomass pyrolysis and the re-polymerization of phenolic oxygenates. Suitable conditions to achieve almost full conversion with a H2 yield of up to 95 % and stability for 160 min on stream, the following have been established: 600 ºC, space time of 30 gcatalyst min gvolatiles-1 and S/B ratio of 3.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)), the Basque Government (IT748-13) and the University of the Basque Country (UFI 11/39). I. Barbarias thanks the University of the Basque Country for her postgraduate grant (UPV/EHU 2016).
dc.language.isoenges_ES
dc.publisherElsevier
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2016-75535-R
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ-2015-69436-R
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.subjectbiomasses_ES
dc.subjectpyrolysises_ES
dc.subjectreforminges_ES
dc.subjecthydrogenes_ES
dc.subjectdeactivationes_ES
dc.subjectbio-oiles_ES
dc.titleRole of operating conditions in the catalyst deactivation in the in-line steam reforming of volatiles from biomass fast pyrolysises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/abs/pii/S0016236117315697es_ES
dc.identifier.doi10.1016/j.fuel.2017.12.002
dc.departamentoesIngeniería química
dc.departamentoeuIngeniaritza kimikoa


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© 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
Except where otherwise noted, this item's license is described as © 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/