Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/32809
DC FieldValueLanguage
dc.contributor.authorDabbawala, Aasif A.-
dc.contributor.authorAl Maksoud, Walid-
dc.contributor.authorAbou-Hamad, Edy-
dc.contributor.authorCharisiou, Nikolaos D.-
dc.contributor.authorConstantinou, Achilleas-
dc.contributor.authorHarkou, Eleana-
dc.contributor.authorLatsiou, Angeliki I.-
dc.contributor.authorAlKhoori, Sara-
dc.contributor.authorHinder, Steve J.-
dc.contributor.authorBaker, Mark A.-
dc.contributor.authorAnjum, Dalaver H.-
dc.contributor.authorKobayashi, Yoji-
dc.contributor.authorGoula, Maria A.-
dc.contributor.authorPolychronopoulou, Kyriaki-
dc.date.accessioned2024-08-21T06:11:37Z-
dc.date.available2024-08-21T06:11:37Z-
dc.date.issued2024-08-01-
dc.identifier.citationChemical Engineering Journal, 2024 vol. 493en_US
dc.identifier.issn13858947-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/32809-
dc.description.abstractThe hydrodeoxygenation (HDO) of bio-oil is one of the potential approaches to produce green diesel. However, HDO catalyst requires the development of bifunctionality which translates to the simultaneous presence of acidic and metal sites for desired catalytic activity and selectivity. Zeolites and their composites are attractive candidates for the conversion of biomass to fuels. In the present work, a series of Ni-incorporated Al2O3-zeolite beta bifunctional composite catalysts with distinct Al2O3 (25–75 wt%) and Ni contents (5–15 wt%) were synthesized via a facile one-pot method directly from nickel acetate, nano-boehmite (γ-AlO(OH)) and the NH4+ form of beta zeolite (NH4+-BZ). The nano-boehmite particles, due to the positive charges on their surface, electrostatically attract negatively charged beta zeolite crystals, which leads to the assembly of a hierarchical pore structure upon calcination. Interestingly, the composite catalysts synthesized were quite homogeneous with uniform dispersion of Ni particles. All composite catalysts were thoroughly characterized using XRD, SEM-EDX, SEM-mapping, HR-TEM, H2-TPR, H2-TPD, NH3-TPD, XPS, 31P MAS NMR, 27Al MAS NMR and N2 sorption analysis. The synthesized composite catalysts with distinct Al2O3 contents showed diverse textural properties, distinct nature of acid sites and improved performance in hydrodeoxygenation of palm oil. Particularly, the Ni/BZ-Al50 (with BZ:Al2O3 = 50:50) composite catalyst significantly enhanced the conversion of palm oil (up to 90%) and yield of n-C15-C18 hydrocarbons (up to 69%) at moderate temperature of 375 °C as compared to 10Ni/BZ catalyst (Conv. = 75%, yield of n-C15-C18 = 52%). The higher catalytic performance realized with composite catalysts can be ascribed to its hierarchical pore structure, moderate acidity (chemisorption studies), tuned acid sites nature (solid state NMR) and homogeneous distribution of active Ni sites (H2 chemisorption) which helps to improve product selectivity by minimizing side reactions. The time-on-stream (TOS) experiments were carried out up to 20 h which clearly showed that composite catalysts are more stable suggesting the lower amount of coke deposition (TPO studies) and suppression of metal sintering.en_US
dc.language.isoenen_US
dc.relation.ispartofChemical Engineering Journalen_US
dc.rights© 2024 Published by Elsevier B.Ven_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAcid sitesen_US
dc.subjectHydrodeoxygenationen_US
dc.subjectNickel, bifunctional catalysten_US
dc.subjectPalm oilen_US
dc.subjectSelective deoxygenationen_US
dc.subjectSolid state NMRen_US
dc.titleTuning of the acid sites in the zeolite-alumina composite Ni catalysts and their impact on the palm oil hydrodeoxygenation reactionen_US
dc.typeArticleen_US
dc.collaborationKhalifa University of Science and Technologyen_US
dc.collaborationKing Abdullah University of Science and Technologyen_US
dc.collaborationUniversity of Western Macedoniaen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationUniversity of Surreyen_US
dc.subject.categoryChemical Engineeringen_US
dc.journalsSubscriptionen_US
dc.countryUnited Arab Emiratesen_US
dc.countrySaudi Arabiaen_US
dc.countryGreeceen_US
dc.countryCyprusen_US
dc.countryUnited Kingdomen_US
dc.subject.fieldEngineering and Technologyen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1016/j.cej.2024.152351en_US
dc.identifier.scopus2-s2.0-85194314185-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85194314185-
dc.relation.volume493en_US
cut.common.academicyear2024-2025en_US
item.openairetypearticle-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.grantfulltextnone-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
crisitem.author.orcid0000-0002-7763-9481-
crisitem.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
crisitem.journal.journalissn1385-8947-
crisitem.journal.publisherElsevier-
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