Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/18969

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Campo DCValorIdioma
dc.contributor.authorMachado, A. V.-
dc.contributor.authorNeves, Isabel C.-
dc.contributor.authorBotelho, Gabriela-
dc.contributor.authorRebelo, P.-
dc.date.accessioned2012-04-27T16:14:58Z-
dc.date.available2012-04-27T16:14:58Z-
dc.date.issued2006-
dc.identifier.issn0014-3057por
dc.identifier.urihttps://hdl.handle.net/1822/18969-
dc.description.abstractThermogravimetric (TGA) and differential scanning calorimetric (DSC) analyses were used to investigate the effect of the acidity behaviour of Y zeolites on the catalytic degradation of polyethylene (PE). The acidity behaviour of these zeolites was modified by ion exchange treatments. Two Y zeolites with similar Si/Al atomic ratios were subjected to an ion exchange treatment using NaNO3 for H-form (HY) and NH4NO3 for Na-form (NaY). The activity and the deactivation behaviour of the Y zeolites were determined in the samples by TGA measurements, using a polymer/catalyst ratio of 9:1. The sample residues obtained after an isothermic TGA, were analysed by DSC, in order to evaluate the crystallinity of each mixture. The HY zeolite, which has the strongest acidity, reduced the onset temperature resulting in more rapid degradation of the polymer. It is shown that the ion exchange treatment over Y zeolites enhances the selective catalytic degradation of polymer in detriment of the rapid deactivation.por
dc.language.isoengpor
dc.publisherElsevier 1por
dc.rightsrestrictedAccesspor
dc.subjectY Zeolitepor
dc.subjectIon exchangepor
dc.subjectPolymer degradationpor
dc.subjectCatalytic crackingpor
dc.subjectDeactivationpor
dc.titleThe effect of acidity behaviour of Y zeolites on the catalytic degradation of polyethylenepor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://www.sciencedirect.com/por
sdum.publicationstatuspublishedpor
oaire.citationStartPage1541por
oaire.citationEndPage1547por
oaire.citationIssue8por
oaire.citationTitleEuropean Polymer Journalpor
oaire.citationVolume42por
dc.identifier.doi10.1016/j.eurpolymj.2006.01.021por
dc.subject.wosScience & Technologypor
sdum.journalEuropean Polymer Journalpor
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