Please use this identifier to cite or link to this item: http://ricaxcan.uaz.edu.mx/jspui/handle/20.500.11845/2602
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dc.contributor20533es_ES
dc.coverage.spatialGlobales_ES
dc.creatorGonzález Castañeda, Daniel Gibran-
dc.creatorSanchez Enríquez, Adriana-
dc.creatorCruz Reyes, Ivan-
dc.creatorCalzada Hernández, Alan Rubén-
dc.creatorSerrano Rosales, Benito-
dc.date.accessioned2021-06-18T04:01:16Z-
dc.date.available2021-06-18T04:01:16Z-
dc.date.issued2019-
dc.identifierinfo:eu-repo/semantics/publishedVersiones_ES
dc.identifier.issn1542-6580es_ES
dc.identifier.urihttp://ricaxcan.uaz.edu.mx/jspui/handle/20.500.11845/2602-
dc.description.abstractSix different Ni-based fluidizable catalysts were synthesized using both incipient impregnation and co- impregnation. Ni-based catalysts were also promoted with 2.0 wt% La or alternatively with 2 wt% Ce. The preparation procedure included catalysts treated at high temperatures and under free of oxygen conditions. Catalysts were characterized using BET, XRD, AA, PSD, TPR, TPD, H2-chemisorption. TPR and H2 chemisorp-tion showed good metal dispersion with 10 nm- 40 nm metal crystallites. Glucose catalytic gasification runs were performed in a CREC Riser Simulator to evaluate the following cata- lysts: (a) 5 %Ni/γ-Al2O3, (b) 5 %Ni-2 %La/γ-Al2O3 and (c) 5 %Ni-2 %Ce/γ-Al2O3. In all cases, the preparation steps involved acid solutions with pHs of 1 and 4. In between consecutive runs, different approaches were considered: (a) A catalyst was regenerated by air, (b) A catalyst was regenerated by air followed by hydrogen pretreatment, (c) A catalyst was reused directly without any regeneration or hydrogen pretreatment. It was observed that Ni-based catalysts, which were subjected after every run, to both, air regeneration and hydro- gen pretreatment, displayed the best yields in close agreement with thermodynamic equilibrium. On the other hand, Ni-based catalysts regenerated with air only, showed the worst hydrogen yields. In between these two- hydrogen yield limits, where catalysts not contacted with air nor hydrogen, with these yields being moderately below chemical equilibrium. This shows that Ni-based fluidizable catalysts can perform on stream for extended periods, requiring limited reactivation with air and H2. This makes of gasification using the catalysts of the present study, a viable process alternative that could be implemented at industrial scale.es_ES
dc.language.isoenges_ES
dc.publisherDe Gruyteres_ES
dc.relationhttps://www.degruyter.com/document/doi/10.1515/ijcre-2019-0104/htmles_ES
dc.relation.urigeneralPublices_ES
dc.rightsAtribución-NoComercial-CompartirIgual 3.0 Estados Unidos de América*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.sourceInternational Journal of Chemical Reactor Engineering Vol 17, No. 11, pp. 1-17es_ES
dc.subject.classificationINGENIERIA Y TECNOLOGIA [7]es_ES
dc.subject.otherhydrogenes_ES
dc.subject.otherglucosees_ES
dc.subject.othernickeles_ES
dc.subject.otherceriumes_ES
dc.subject.otherlanthanumes_ES
dc.subject.othergasificationes_ES
dc.titleCatalytic Steam Gasification of Glucose for Hydrogen Production Using Stable Based Ni on a γ–Alumina Fluidizable Catalystes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
Appears in Collections:*Documentos Académicos*-- Doc. en Ciencias de la Ing.

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