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dc.contributor.authorDíez-Martín, Laura-
dc.contributor.authorLópez Sebastián, José Manuel-
dc.contributor.authorFernández García, José Ramón-
dc.contributor.authorMartínez Berges, Isabel-
dc.contributor.authorGrasa Adiego, Gemma-
dc.contributor.authorMurillo Villuendas, Ramón-
dc.date.accessioned2019-06-26T10:31:16Z-
dc.date.available2019-06-26T10:31:16Z-
dc.date.issued2018-06-15-
dc.identifierdoi: 10.1016/j.cej.2018.06.049-
dc.identifierissn: 1385-8947-
dc.identifier.citationChemical Engineering Journal 350: 1010-1021 (2018)-
dc.identifier.urihttp://hdl.handle.net/10261/184875-
dc.description7 Figures, 2 Tables.-- © 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.description.abstractThe three main reaction stages of a H2 production process based on the combination of the CaO/CaCO3 and Cu/CuO loops have been experimentally studied in a lab scale fixed bed reactor. The solid bed contained the three functional materials required to run the process, namely a commercial Ni-based catalyst, a CaO-Ca12Al14O33 CO2 sorbent and a CuO-Al2O3 material in a proportion that resulted in a bed with 43.3% wt. CuO, 25.6% wt. CaO and 1.7% wt. Ni. The system was able to convert 13.5 kg CH4 h−1 kg Ni−1, at 675 °C producing a gas stream with a 93.5% vol. H2 at 10 bar. The Cu-based material presented high oxidation kinetics, being totally converted in a narrow reaction front with a highly diluted air stream at 10 bar. The Cu-based material presented also fast reduction kinetics and it was completely converted with a fuel gas with typical composition of a Steam Methane Reforming stage at high temperature. A Cu/Ca molar ratio of 2 allowed for calcination efficiencies over 85% molar basis at the CO and H2 break-through, and 95% of the CO2 from CaCO3 exited the reactor at CH4 break-through. The experimental results have been validated with an existing pseudo homogeneous reactor model that had been developed in previous works for the three reaction stages. The model was able to predict product gas compositions, bed breakthrough, and temperature profiles along bed.-
dc.description.sponsorshipThis work acknowledges the support by European Union Seventh Frame Programme FP7 under Grant agreement n° 608512 (ASCENT Project). Laura Díez acknowledges the FPI fellowship (ENE 2012-37936-CO2-01, BES-2013-064616 financed by MICINN). The authors want also to thank the support from the Regional Aragon Government (DGA) under the research groups support program.-
dc.publisherElsevier BV-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/608512-
dc.relation.isversionofPostprint-
dc.rightsopenAccessen_EN
dc.subjectCH4 sorption enhanced reforming-
dc.subjectFixed bed reactor-
dc.subjectPressurized H2 production-
dc.subjectCa/Cu cycle-
dc.subjectCO2 capture-
dc.titleComplete Ca/Cu cycle for H2 production via CH4 sorption enhanced reforming in a Lab-Scale fixed bed reactor-
dc.typeartículo-
dc.identifier.doi10.1016/j.cej.2018.06.049-
dc.date.updated2019-06-26T10:31:16Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.rights.licensehttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.contributor.funderEuropean Commission-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.contributor.funderGobierno de Aragón-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100010067es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.contributor.orcidLópez Sebastián, José Manuel [0000-0002-6203-8835]-
dc.contributor.orcidFernández García, José Ramón [0000-0001-9801-7043]-
dc.contributor.orcidGrasa Adiego, Gemma [0000-0002-4242-5846]-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeartículo-
item.cerifentitytypePublications-
item.grantfulltextopen-
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