Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2304
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dc.contributor.authorAbou Rached, Jihaneen_US
dc.contributor.authorEl Hayek, Christelleen_US
dc.contributor.authorDahdah, Elianeen_US
dc.contributor.authorGennequin, Cédricen_US
dc.contributor.authorAouad, Sameren_US
dc.contributor.authorTidahy, Haingomalala Lucetteen_US
dc.contributor.authorEstephane, Janeen_US
dc.contributor.authorNsouli, Bilalen_US
dc.contributor.authorAboukaïs, Antoineen_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.date.accessioned2020-12-23T09:10:32Z-
dc.date.available2020-12-23T09:10:32Z-
dc.date.issued2017-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2304-
dc.description.abstractNixMg6−xAl1.8Ce0.2 (with 0 ≤ x ≤ 6) mixed oxides catalysts were prepared by hydrotalcite route. All the oxides were calcined at 800 °C and characterized by different physico-chemical methods. The catalysts are then reduced before their use in the steam reforming of toluene. The XRD and TG/DTA confirmed the formation of the hydrotalcite structure for the non-calcined samples. The N2 adsorption/desorption results revealed that all catalysts correspond to mesoporous materials. The study by temperature programmed reduction (H2-TPR) showed that the reducibility of the catalysts is influenced by the nickel content. The CO2-TPD results showed that the catalyst with high magnesium content present the highest basicity. The Ni2Mg4Al1.8Ce0.2 shows the best toluene conversion among all the catalysts and it was then compared to a non-promoted catalyst. The spent catalysts were characterized by TPO, TG/DTA and XRD and they didn't reveal any coke formation.en_US
dc.format.extent11 p.en_US
dc.language.isoengen_US
dc.subjectHydrogenen_US
dc.subjectSteam reformingen_US
dc.subjectNickelen_US
dc.subjectHydrotalciteen_US
dc.subjectBasicityen_US
dc.subject.lcshTolueneen_US
dc.titleNi based catalysts promoted with cerium used in the steam reforming of toluene for hydrogen productionen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.ijhydene.2016.10.053-
dc.contributor.affiliationDepartment of Chemistryen_US
dc.contributor.affiliationDepartment of Chemical Engineeringen_US
dc.description.volume42en_US
dc.description.issue17en_US
dc.description.startpage12829en_US
dc.description.endpage12840en_US
dc.date.catalogued2017-10-26-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.ijhydene.2016.10.053en_US
dc.identifier.OlibID174576-
dc.relation.ispartoftextInternational journal of hydrogen energyen_US
dc.provenance.recordsourceOliben_US
Appears in Collections:Department of Chemistry
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