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Morphological changes in segmented polyurethane elastomers by varying the NCO/OH ratio

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dc.contributor.author Spathis, G en
dc.contributor.author Niaounakis, M en
dc.contributor.author Kontou, E en
dc.contributor.author Apekis, L en
dc.contributor.author Pissis, P en
dc.contributor.author Christodoulides, C en
dc.date.accessioned 2014-03-01T01:09:59Z
dc.date.available 2014-03-01T01:09:59Z
dc.date.issued 1994 en
dc.identifier.issn 0021-8995 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/11279
dc.subject.classification Polymer Science en
dc.subject.other Calorimetry en
dc.subject.other Crosslinking en
dc.subject.other Molecular weight en
dc.subject.other Morphology en
dc.subject.other Polarization en
dc.subject.other Polymerization en
dc.subject.other Polyurethanes en
dc.subject.other Separation en
dc.subject.other Spectroscopy en
dc.subject.other Differential scanning calorimetry en
dc.subject.other Fourier transform infrared spectroscopy en
dc.subject.other Hydrogen bonding en
dc.subject.other Phase separation en
dc.subject.other Relaxation mechanism en
dc.subject.other Segmented polyurethane elastomers en
dc.subject.other Thermally stimulated depolarization current en
dc.subject.other Thermoplastic polyurethane en
dc.subject.other Elastomers en
dc.title Morphological changes in segmented polyurethane elastomers by varying the NCO/OH ratio en
heal.type journalArticle en
heal.identifier.primary 10.1002/app.1994.070540701 en
heal.identifier.secondary http://dx.doi.org/10.1002/app.1994.070540701 en
heal.language English en
heal.publicationDate 1994 en
heal.abstract The morphological changes induced to segmented polyurethane elastomers by varying the NCO/OH ratio during the second step of polymerization, while keeping constant the total hard-segment content (similar to 30%), were studied by means of Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and the thermally stimulated depolarization current method (TSDC). The DSC results gave evidence for the existence of phase separation in thermoplastic polyurethanes, whereas the elastomeric ones appeared to form a more homogeneous network. The FTIR results gave additional evidence regarding phase separation by detecting the strength of the hydrogen bonds. Moreover, an attempt was made to assess the relative contribution made to the hydrogen bonding in such systems by the two potential accepters: ester and urethane carbonyls. The TSDC results gave a relaxation mechanism that is due to interfacial (Maxwell-Wagner-Sillars) polarization, providing evidence of the existence of an interfacial phase. The introduced secondary chemical cross-links was found to affect mainly the irregularly packed hard domains and to form a more homogeneous network at higher values of the NCO/OH ratio. (C) 1994 John Wiley and Sons, Inc. en
heal.publisher John Wiley & Sons Inc, New York, NY, United States en
heal.journalName Journal of Applied Polymer Science en
dc.identifier.doi 10.1002/app.1994.070540701 en
dc.identifier.isi ISI:A1994PM24800001 en
dc.identifier.volume 54 en
dc.identifier.issue 7 en
dc.identifier.spage 831 en
dc.identifier.epage 842 en


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