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dc.contributor.authorUmar, Ahmed
dc.contributor.authorIrvine, John T.S.
dc.date.accessioned2021-01-25T12:30:08Z
dc.date.available2021-01-25T12:30:08Z
dc.date.issued2020-11-06
dc.identifier.citationUmar , A & Irvine , J T S 2020 , ' Gasification of glycerol over Ni/γ-Al 2 O 3 for hydrogen production : tailoring catalytic properties to control deactivation ' , Catalysis for Sustainable Energy , vol. 7 , no. 1 , pp. 65-74 . https://doi.org/10.1515/cse-2020-0006en
dc.identifier.issn2084-6819
dc.identifier.otherPURE: 272471881
dc.identifier.otherPURE UUID: 07b47942-d174-49c4-8ad0-0cd05c4d86a2
dc.identifier.otherJisc: e4ff57f080a34beca84806db403ceb9a
dc.identifier.otherORCID: /0000-0002-8394-3359/work/87403906
dc.identifier.urihttps://hdl.handle.net/10023/21314
dc.descriptionAuthors thank the Petroleum Technology Development Fund (PTDF), Nigeria for funding this research and the University of St Andrews, Scotland UK for the consideration to work with them and to use their facilities.en
dc.description.abstractThe effects of catalyst loading, calcination and reaction temperatures on the structural properties and catalytic behavior of Ni/γ-Al2O3 catalyst system in relation to steam reforming of glycerol and catalyst deactivation were investigated. The results showed that catalyst loading, reaction and calcination temperatures had a profound influence on the structure and catalytic activity in glycerol conversion. Use of high calcination temperature (900-1000 °C) led to phase transformation of the active Ni/Al2O3 to less active spinel specie NiAl2O4 that resulted in a successive change of texture and color. The particle size growth and phase change at this temperature were responsible for the catalyst deactivation and low performance especially among the catalyst calcined at high temperatures. Conversely, at low reaction temperatures, catalyst surfaces were marred by carbon deposition. Whilethe polymeric carbon deposited at metal-support interface was associated with low reaction temperatures, high reaction temperatures were characterized predominantly by both amorphous carbon deposited on the active metal surface and polymeric or graphitic carbon deposited at metal-support interface respectively. Calcination temperature showed no significant influence on the location and type of coke deposited on the catalyst surface. Hence, catalyst loading, calcination and reaction temperatures could be tailored to enhance structural and catalytic properties and guard against catalyst deactivation.
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofCatalysis for Sustainable Energyen
dc.rightsCopyright © 2020 Ahmed Umar, John T.S. Irvine, published by De Gruyter. This work is licensed under the Creative Commons Attribution alone 4.0 License.en
dc.subjectSteam reformingen
dc.subjectBiomass feedstocken
dc.subjectGaseous biofuelen
dc.subjectSupported catalysten
dc.subjectFuel cellen
dc.subjectCokingen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subjectSDG 7 - Affordable and Clean Energyen
dc.subject.lccQDen
dc.titleGasification of glycerol over Ni/γ-Al2O3 for hydrogen production : tailoring catalytic properties to control deactivationen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Centre for Designer Quantum Materialsen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1515/cse-2020-0006
dc.description.statusPeer revieweden


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