Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/7294
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dc.contributor.authorHamdan, Mohammaden_US
dc.contributor.authorHalawy, Layalen_US
dc.contributor.authorHijazi, Aymanen_US
dc.contributor.authorAouad, Sameren_US
dc.contributor.authorZeaiter, Josephen_US
dc.date.accessioned2024-03-27T09:37:13Z-
dc.date.available2024-03-27T09:37:13Z-
dc.date.issued2024-04-03-
dc.identifier.issn03603199-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/7294-
dc.description.abstractZinc-promoted nickel catalysts on Ultra-Stable Y (USY) zeolite support are tested for their efficacy towards methane pyrolysis. The un-promoted catalyst obtained a conversion of 65.8%, which dropped to 57.3% at the end of the experiment. However, addition of 5 wt% Zn promoter increased the conversion to 67.7%, with no discernible loss in activity after 60 h on-stream. XPS analysis indicated evidence of electronic interaction between the Ni and Zn metals, and the addition of Zn caused a reduction in the metal-support interactions of the catalyst as revealed in TPR and XRD analyses. The catalytic activity of the 50Ni–5Zn/USY also remained completely stable for 60 h even after the operating temperature was increased to 650 °C and the partial pressure of methane in the inlet increased to 80%, at a High gas hour space velocity of 120 L/gcat.h. Analysis of the spent 50Ni–5Zn/USY catalyst revealed the presence of Ni–Zn carbides that may have contributed to the increase in activity, as well as the formation of large quantities of highly graphitic and ordered multi-walled carbon nanotubes produced by the tip-growth mechanism which have been shown to prolong catalyst lifetime on-stream.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.subjectFilamentous carbonen_US
dc.subjectHydrogenen_US
dc.subjectMethane pyrolysisen_US
dc.subjectNi–Zn catalysten_US
dc.subjectZeoliteen_US
dc.titleHighly-stable Ni–Zn catalyst on USY zeolite support for low temperature methane pyrolysisen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1016/j.ijhydene.2024.02.370-
dc.identifier.scopus2-s2.0-85186653336-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85186653336-
dc.contributor.affiliationDepartment of Chemistryen_US
dc.description.volume61en_US
dc.description.startpage840en_US
dc.description.endpage850en_US
dc.date.catalogued2024-03-27-
dc.description.statusPublisheden_US
dc.identifier.ezproxyURLhttp://ezsecureaccess.balamand.edu.lb/login?url=https://doi.org/10.1016/j.ijhydene.2024.02.370en_US
dc.relation.ispartoftextInternational Journal of Hydrogen Energyen_US
crisitem.author.parentorgFaculty of Arts and Sciences-
Appears in Collections:Department of Chemistry
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