Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2393
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dc.contributor.authorLabaki, Madonaen_US
dc.contributor.authorAouad, Sameren_US
dc.contributor.authorHany, Saraen_US
dc.contributor.authorAbou Serhal, Cynthiaen_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.contributor.authorAbouKais, Antoineen_US
dc.date.accessioned2020-12-23T09:12:21Z-
dc.date.available2020-12-23T09:12:21Z-
dc.date.issued2019-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2393-
dc.description.abstract4 wt% Rh/CeO2 catalysts were prepared by two different methods: deposition–precipitation (DP) and impregnation (Imp). X-ray diffraction (XRD), differential scanning calorimetry and thermogravimetry (DSC-TG), temperature-programmed reduction (TPR), and electron paramagnetic resonance (EPR) were used for physicochemical characterization. The solids were tested in propylene and carbon black oxidation reactions. The 4%Rh/CeO2 (DP) showed better catalytic performance in both reactions compared to the catalyst prepared by the impregnation method. The XRD technique evidenced the formation of Rh2O3 phase in the DP-solid after calcination of this latter at 400 °C for 4 h. EPR evidenced, only in the DP-solid, the presence of O2− species in interaction with the CeO2 surface whereas Rh4+ ions in the form of clusters were identified in both solids. The TPR technique showed that the DP-solid was reduced by hydrogen at lower temperature compared to the impregnated one. The higher catalytic performance of the DP-solid was attributed to the presence of O2− species along with the presence of Rh2O3 phase in ceria and to the better reducibility and lower particle size of the rhodium species.en_US
dc.language.isoengen_US
dc.subjectCeO2en_US
dc.subjectDeposition-precipitationen_US
dc.subjectImpregnationen_US
dc.subjectO2−en_US
dc.subjectRh2O3en_US
dc.subject.lcshOxidationen_US
dc.titlePhysico-chemical investigation of catalytic oxidation sites in 4%Rh/CeO2 catalysts prepared by impregnation and deposition-precipitation methodsen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.chemphys.2019.110472-
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume527en_US
dc.description.startpage1en_US
dc.description.endpage7en_US
dc.date.catalogued2020-02-17-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.chemphys.2019.110472en_US
dc.identifier.OlibID252402-
dc.relation.ispartoftextJournal of chemical physicsen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Chemistry
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