Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2052
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dc.contributor.authorDahdah, Elianeen_US
dc.contributor.authorAouad, Sameren_US
dc.contributor.authorGennequin, Cédricen_US
dc.contributor.authorEstephane, Janeen_US
dc.contributor.authorNsouli, Bilalen_US
dc.contributor.authorAbouKais, Antoineen_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.date.accessioned2020-12-23T09:05:30Z-
dc.date.available2020-12-23T09:05:30Z-
dc.date.issued2018-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2052-
dc.description.abstractRu-Mg-Al hydrotalcite-derived mixed oxides were synthesized using two preparation methods. The grafted catalyst was prepared by co-precipitation of the Ru/Mg/Al precursors at a constant pH. The impregnated catalyst was prepared by wet-impregnation of a calcined Mg-Al support with the Ru precursor (Ru(NO) (NO3)3). Both catalysts were calcined at 600 °C and characterized by X-ray diffraction, CO2- temperature programmed desorption and H2-temperature programmed reduction techniques. Catalytic activities were compared in the glycerol steam reforming reaction (400–700 °C, WGFR 9:1, flow rate: 0.075 ml/min) followed by a short-term stability test at 600 °C. The impregnated catalyst demonstrated a superior activity beyond 600 °C. This difference in activity was attributed to the easier accessibility of the active phase resulting from the preparation method. Short-term stability tests revealed deactivation of both catalysts as a result of coke formation.en_US
dc.language.isoengen_US
dc.subjectRutheniumen_US
dc.subjectHydrotalciteen_US
dc.subjectGlycerolen_US
dc.subjectReformingen_US
dc.subject.lcshCatalystsen_US
dc.titleGlycerol steam reforming over Ru-Mg-Al hydrotalcite-derived mixed oxides: role of the preparation method in catalytic activityen_US
dc.typeJournal Articleen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.contributor.affiliationDepartment of Chemical Engineeringen_US
dc.description.volume43en_US
dc.description.issue43en_US
dc.description.startpage19864en_US
dc.description.endpage19872en_US
dc.date.catalogued2019-06-07-
dc.description.statusPublisheden_US
dc.identifier.OlibID192260-
dc.relation.ispartoftextInternational journal of hydrogen energyen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
crisitem.author.parentorgFaculty of Engineering-
Appears in Collections:Department of Chemistry
Department of Chemical Engineering
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