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Some elastic and thermoelastic properties of two organophosphazene polymers

dc.contributor.authorMark, J. E.en_US
dc.contributor.authorYu, C. U.en_US
dc.date.accessioned2006-04-28T18:09:35Z
dc.date.available2006-04-28T18:09:35Z
dc.date.issued1977-02en_US
dc.identifier.citationMark, J. E.; Yu, C. U. (1977)."Some elastic and thermoelastic properties of two organophosphazene polymers." Journal of Polymer Science: Polymer Physics Edition 15(2): 371-378. <http://hdl.handle.net/2027.42/38662>en_US
dc.identifier.issn0098-1273en_US
dc.identifier.issn1542-9385en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38662
dc.description.abstractSamples of the alkoxyphosphazene polymer [P(OCH 3 ) 2 [bond]N[bond]] x and the aryloxyphosphazene polymer [P(OC 6 H 5 )(O- p -C 6 H 4 C 2 H 5 )[bond]N[bond]] x were crosslinked using Γ-radiation. The resulting elastomeric networks were characterized, in elongation, with regard to both their stress-strain relationships and their stress-temperature (“thermoelastic”) properties. Values of the ratio 2 C 2 /2 C 1 of Mooney–Rivlin constants used to characterize the stress-strain isotherms were found to be similar to those of other elastomeric networks of comparable degree of crosslinking. The thermoelastic data show the energetic component of the retractive force to be positive for the alkoxy polymer, but negative for the aryloxy polymer. Although it is not difficult to suggest a possible molecular explanation for some of these thermoelastic results, a definitive interpretation would require reliable information on the conformational characteristics of the skeletal bonds in the polyphosphazene chain.en_US
dc.format.extent491827 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherPhysicsen_US
dc.subject.otherPolymer and Materials Scienceen_US
dc.titleSome elastic and thermoelastic properties of two organophosphazene polymersen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry and the Macromolecular Research Center, The University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Chemistry and the Macromolecular Research Center, The University of Michigan, Ann Arbor, Michigan 48109en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38662/1/180150215_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/pol.1977.180150215en_US
dc.identifier.sourceJournal of Polymer Science: Polymer Physics Editionen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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