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Positronium formation in semicrystalline poly(ethylene terephthalate)

dc.contributor.authorLi Xie,en_US
dc.contributor.authorGidley, David W.en_US
dc.contributor.authorHristov, Hristo A.en_US
dc.contributor.authorYee, Albert F.en_US
dc.date.accessioned2006-04-10T18:24:48Z
dc.date.available2006-04-10T18:24:48Z
dc.date.issued1994-01en_US
dc.identifier.citationLi Xie, , Gidley, David W., Hristov, Hristo A., Yee, Albert F. (1994/01)."Positronium formation in semicrystalline poly(ethylene terephthalate)." Polymer 35(1): 14-17. <http://hdl.handle.net/2027.42/31851>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TXW-48FC1KJ-28J/2/ee1cdba83449d02b2d6ff371cc315abben_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31851
dc.description.abstractThe probability of positronium (Ps) formation in semicrystalline poly(ethylene terephthalate) (PET), has been investigated by means of positron annihilation lifetime spectroscopy (p.a.l.s.). The p.a.l.s. data are correlated with the structural characteristics of the samples, such as crystalline content, interlamellar spacing and lamella thickness. The results show an approximately linear decrease of the intensity (I3) of the long-lived orthopositronium (o-Ps) component with an increase in the crystalline content up to 53%, while the lifetime remains practically constant. It seems that the other structural parameters do not affect the Ps formation. The decrease of I3 cannot be completely accounted for if one assumes that o-Ps localizes in the amorphous phase only. It is suggested that the o-Ps also forms in the crystalline regions, due to the inhomogeneous electron density distribution along the c-axis of the PET lattice.en_US
dc.format.extent441915 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titlePositronium formation in semicrystalline poly(ethylene terephthalate)en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelManagementen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelEconomicsen_US
dc.subject.hlbtoplevelBusinessen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Physics, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Physics, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering, University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31851/1/0000800.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0032-3861(94)90042-6en_US
dc.identifier.sourcePolymeren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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