Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/1715
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dc.contributor.authorAoun, Amalen_US
dc.contributor.authorAouad, Sameren_US
dc.contributor.authorNakat, John Elen_US
dc.contributor.authorKhoury, Bilal Elen_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.contributor.authorAboukaïs, Antoineen_US
dc.date.accessioned2020-12-23T08:58:09Z-
dc.date.available2020-12-23T08:58:09Z-
dc.date.issued2011-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/1715-
dc.description.abstractDifferent catalysts based on ruthenium impregnated on hydrotalcites (Ru/CoxMgyAl2-HT) were prepared by wet impregnation from aqueous nitrosyl nitrate solutions and activated under air at 600 °C for 4 h. The reactivity of the catalysts was evaluated in the oxidation of carbon black (CB). The results showed that the best catalyst decreased the temperature at which the rate of carbon black oxidation is the highest by about 150 °C. This good reactivity was attributed to the formation of easily reducible ruthenium and cobalt oxide species at the surface of the support. The addition of ruthenium made the reduction of surface and bulk cobalt oxides possible at lower temperatures.en_US
dc.format.extent5 p.en_US
dc.language.isoengen_US
dc.subjectHydrotalciteen_US
dc.subjectRutheniumen_US
dc.subject.lcshCarbon blacken_US
dc.subject.lcshCatalystsen_US
dc.subject.lcshOxidationen_US
dc.titleCatalytic oxidation of carbon black over Ru/CoxMgyAl2 catalystsen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.phpro.2011.10.001-
dc.contributor.affiliationDepartment of Chemistryen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume21en_US
dc.description.startpage1en_US
dc.description.endpage5en_US
dc.date.catalogued2017-11-20-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.phpro.2011.10.001en_US
dc.identifier.OlibID175084-
dc.relation.ispartoftextJournal of physics procediaen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
crisitem.author.parentorgFaculty of Arts and Sciences-
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Chemistry
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