Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/1742
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dc.contributor.authorEstephane, Janeen_US
dc.contributor.authorAouad, Sameren_US
dc.contributor.authorHany, Saraen_US
dc.contributor.authorKhoury, Bilal Elen_US
dc.contributor.authorGennequin, Cédricen_US
dc.contributor.authorZakhem, Henri Elen_US
dc.contributor.authorEl Nakat, Jen_US
dc.contributor.authorAboukaïs, Antoineen_US
dc.contributor.authorAbi Aad, Edmonden_US
dc.date.accessioned2020-12-23T08:58:39Z-
dc.date.available2020-12-23T08:58:39Z-
dc.date.issued2015-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/1742-
dc.description.abstractThe wet impregnation method was used to prepare ZSM5 supported nickel and/or cobalt monometallic and bimetallic catalysts with a 7 wt.% total metal loading. The CO2 reforming of methane reaction was carried out in the 600 °C–800 °C temperature range over the different catalysts (GHSV 60000 mL g−1 hr−1). The cobalt containing catalysts favored the reverse water gas shift reaction at high temperature and cobalt acted as a synergist to nickel, as overall, bimetallic catalysts showed better catalytic performance. Carbon deposition was less expressed over catalysts with high cobalt content. Following 12 h on stream at 700 °C, the bimetallic catalyst with cobalt to nickel ratio of 2, showed high CO2 and CH4 conversions (∼60%) accompanied with the lowest carbon deposition (5%). The thermal analysis of aged catalysts showed that among the deposited carbon species, it is the carbon present in the proximity of nickel and/or cobalt catalytic sites that is responsible of deactivation.en_US
dc.language.isoengen_US
dc.subjectCatalyst deactivationen_US
dc.subjectDry reformingen_US
dc.subjectNickelen_US
dc.subjectCobalten_US
dc.subjectCarbon depositionen_US
dc.subject.lcshZeolitesen_US
dc.titleCO2 reforming of methane over Ni-Co/ZSM5 catalysts. Aging and carbon deposition studyen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.ijhydene.2015.05.147-
dc.contributor.affiliationDepartment of Chemical Engineeringen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.contributor.affiliationDepartment of Chemistryen_US
dc.contributor.affiliationDepartment of Chemical Engineeringen_US
dc.description.volume40en_US
dc.description.issue30en_US
dc.description.startpage9201en_US
dc.description.endpage9208en_US
dc.date.catalogued2017-10-18-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.ijhydene.2015.05.147en_US
dc.identifier.OlibID174407-
dc.relation.ispartoftextInternational journal of hydrogen energyen_US
dc.provenance.recordsourceOliben_US
crisitem.author.parentorgFaculty of Engineering-
crisitem.author.parentorgFaculty of Arts and Sciences-
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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