Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2727
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dc.contributor.authorDahdah, Elianeen_US
dc.contributor.authorEstephane, Janeen_US
dc.contributor.authorGennequin, Cédricen_US
dc.contributor.authorAbouKais, Antoineen_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.contributor.authorAouad, Sameren_US
dc.date.accessioned2020-12-23T09:19:21Z-
dc.date.available2020-12-23T09:19:21Z-
dc.date.issued2020-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2727-
dc.description.abstractThe effect of the zirconia structure in Ni/ZrO2 catalysts on the glycerol steam reforming (GSR) reaction was studied. A tetragonal zirconia support was synthesized via a hydrolysis technique and loaded with 5 wt% Ni via a wet-impregnation method. Similarly, a commercial monoclinic zirconia support was also impregnated with 5 wt% Ni. Following calcination at 600 °C, physico-chemical properties of the prepared catalysts were investigated by X-Ray Diffraction (XRD), H2-Temperature Programmed Reduction (H2-TPR) and CO2-Temperature Programmed Desorption (CO2-TPD) techniques. The catalysts were then tested in the GSR reaction in the 400–700 °C range with a steam to glycerol molar ratio of 9:1 and a flow rate of 0.025 mL/min. The monoclinic catalyst exhibited a better performance giving higher hydrogen yields and glycerol conversions. This was attributed to an improved reducibility of Ni in this catalyst. Stability tests at 600 °C revealed the deactivation of the tetragonal catalyst during 6 h as a result of the formation of encapsulating coke which blocked active Ni metal sites. The monoclinic catalyst, exhibiting the formation of only filamentous coke, remained relatively stable for 24 h.en_US
dc.language.isoengen_US
dc.subjectGlycerolen_US
dc.subjectHydrogenen_US
dc.subjectNickelen_US
dc.subjectReformingen_US
dc.subjectZirconiaen_US
dc.titleZirconia supported nickel catalysts for glycerol steam reforming: effect of zirconia structure on the catalytic performanceen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.ijhydene.2019.12.019-
dc.contributor.affiliationDepartment of Chemical Engineeringen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume45en_US
dc.description.issue7en_US
dc.description.startpage4457en_US
dc.description.endpage4467en_US
dc.date.catalogued2020-06-04-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.ijhydene.2019.12.019en_US
dc.identifier.OlibID253064-
dc.relation.ispartoftextInternational journal of hydrogen energyen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Engineering-
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Chemical Engineering
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