Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2543
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dc.contributor.authorAouad, Sameren_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.contributor.authorAboukaïs, Antoineen_US
dc.date.accessioned2020-12-23T09:15:22Z-
dc.date.available2020-12-23T09:15:22Z-
dc.date.issued2009-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2543-
dc.description.abstractRu/CeO2 catalysts with Ru loading of 1–5 wt.% were prepared by wet impregnation from aqueous ruthenium (III) nitrosyl nitrate solution and activation with an air flow at 600 °C for 4 h. This activation resulted in a considerable reactivity for the catalytic oxidation of carbon black (CB) (T50% ∼350 °C "tight contact" mixtures and T50% ∼515 °C "loose contact" mixtures) and volatile organic compounds (VOCs) (T50% = 175 °C for propene, T50% = 215 °C for toluene). When carbon black oxidation was conducted under "propene (6000 ppm) + air" or "toluene (2000 ppm) + air" flow, the elimination of an important part of CB was observed at relatively low temperatures comparing to its elimination under pure air flow. These temperatures correspond to the total oxidation of the VOC present in the reactant gases. Carbon black total elimination was also investigated under isotherm conditions in the presence and in the absence of propene. Total elimination occurred during shorter times when combustion was performed under propene. TPR study showed that ruthenium species present in the catalysts after activation reduces at relatively low temperatures (<100 °C) and that from a Ru loading of 1.5 wt.%, agglomerated ruthenium oxide was formed and that this latter is more difficult to reduce (>100 °C).en_US
dc.format.extent7 p.en_US
dc.language.isoengen_US
dc.subjectRutheniumen_US
dc.subjectTPRen_US
dc.subjectXRDen_US
dc.subjectVOCen_US
dc.subject.lcshCarbon blacken_US
dc.subject.lcshCatalystsen_US
dc.titleSimultaneous oxidation of carbon black and volatile organic compounds over Ru/CeO2 catalystsen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.apcatb.2008.10.002-
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume88en_US
dc.description.issue3-4en_US
dc.description.startpage249en_US
dc.description.endpage256en_US
dc.date.catalogued2017-11-21-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.apcatb.2008.10.002en_US
dc.identifier.OlibID175091-
dc.relation.ispartoftextApplied catalysis B: Environmentalen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Chemistry
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