Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/33197
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dc.contributor.authorAdamou, Panayiota-
dc.contributor.authorHarkou, Eleana-
dc.contributor.authorBumajdad, Ali-
dc.contributor.authorDe Jong, Xander-
dc.contributor.authorVan Haute, Maarten-
dc.contributor.authorConstantinou, Achilleas-
dc.contributor.authorAl-Salem, Sultan Majed-
dc.date.accessioned2024-11-21T07:54:36Z-
dc.date.available2024-11-21T07:54:36Z-
dc.date.issued2024-04-16-
dc.identifier.citationACS Omega, 2024, vol. 9 , iss. 17 , pp. 19057-19062en_US
dc.identifier.issn24701343-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/33197-
dc.description.abstractThe dramatic increase in plastics production, coupled with a low recycling and recovery rate, has been a major challenge for sustainable practices and combating climate change. Hydrotreatment processing to upgrade fuel oils is a well-known process in the petroleum industry. In this work, we aim to investigate the catalyst properties before and after the hydrotreatment of pyrolysis oil derived from plastics, namely, linear low-density polyethylene, as no such report is available in the literature. Granular and powder forms of the Pt/Al2O3 catalyst were used in this study with characterization methods executed as such: transmission electron microscopy, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and IR-RIS. XRD data show that the crystallinity of the catalyst support was unaffected by the hydrotreatment without any residues left, as the characteristic diffraction peaks were indicated for the crystalline phase of the support as 37.4, 39.8, 46.3, and 67.3°. In addition, the TGA experiments revealed that the carbon deposition on the spent catalyst was higher, as indicated by the higher weight loss (15.359%) compared to the fresh catalyst sample (11.43%). XPS analysis showed that the carbon deposition is more intense on the granular spent catalyst, as the intensity of the peaks is some 15 times greater than the peaks from the fresh catalyst. Also, compared to the observed peaks of the powder catalyst, less coke is formed. The band at 1624.05 cm-1 from the IR-RIS spectra was attributed to a shifted C=O band from the coke formation. The extension of these investigations using different catalysts to improve their characteristics and performance and to inhibit coke deposition will contribute to the incorporation of such processes in industry as well as the cost of fuels.en_US
dc.formatPDFen_US
dc.language.isoenen_US
dc.relation.ispartofACS Omegaen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCatalystsen_US
dc.subjectCokeen_US
dc.subjectPlatinumen_US
dc.subjectX-ray photoelectron spectroscopyen_US
dc.titleEffect of Polyethylene Pyrolysis Oil Hydrotreatment on the Pt/Al2O3 Catalyst: Experimental Characterizationen_US
dc.typeArticleen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationKuwait Universityen_US
dc.collaborationKuwait Petroleum Research and Technology B.V.en_US
dc.collaborationKuwait Institute for Scientific Researchen_US
dc.subject.categoryClinical Medicineen_US
dc.journalsOpen Accessen_US
dc.countryCyprusen_US
dc.countryKuwaiten_US
dc.countryNetherlandsen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1021/acsomega.3c09729en_US
dc.identifier.pmid38708201-
dc.identifier.scopus2-s2.0-85190745500-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85190745500-
dc.relation.issue17en_US
dc.relation.volume9Oen_US
cut.common.academicyear2024-2025en_US
dc.identifier.spage19057en_US
dc.identifier.epage19062en_US
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypearticle-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.deptDepartment of Chemical Engineering-
crisitem.author.facultyFaculty of Geotechnical Sciences and Environmental Management-
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.author.parentorgFaculty of Geotechnical Sciences and Environmental Management-
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