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dc.rights.licenseopen
hal.structure.identifierDept Chem Engn & Mat Sci [Univ Minnesota]
dc.contributor.authorALFONSO, C. Guillermo
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorFLEURY, Guillaume
hal.structure.identifierMedtronic SNT
dc.contributor.authorCHAFFIN, Kimberly A.
hal.structure.identifierDept Chem Engn & Mat Sci [Univ Minnesota]
dc.contributor.authorBATES, Frank S.
dc.date.accessioned2020
dc.date.available2020
dc.date.created2010
dc.date.issued2010
dc.identifier.issn0024-9297
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20505
dc.description.abstractEnWe report the synthesis and characterization of fully saturated hydrocarbon block copolymer thermoplastic elastomers with competitive mechanical properties and attractive processing features, Block copolymers containing glassy poly(cyclohexylethylene) (C), elastomeric poly(ethylene-alt-propylene) (P), and semicrystalline poly(ethylene) (E) were produced in a CEC-P-CEC heptablock architecture, denoted XPX, by anionic polymerization and catalytic hydrogenation, The X blocks contain equal volume fractions of C and F. totaling 40%-60% of the material overall. All the XPX polymers are disordered above the melt temperature for E(T(m,E) congruent to 95 degrees C) as evidenced by SAXS and dynamic mechanical spectroscopy measurements, Cooling below results in crystallization of the E blocks, which induces microphase segregation of E, C, and P into a complex morphology with a continuous rubbery domain and randomly arranged hard domains as shown by TEM. This mechanism of segregation decouples the processing temperature from the XPX molecular weight up to a limiting value. Tensile mechanical testing (simple extension and cyclic loading) demonstrates that the tensile strength (ca. 30 MPa) and strain at break (> 500%) are comparable to the behavior of CPC triblock thermoplastic elastomers of similar molecular weight and glass content. However, in the CPC materials, processability is constrained by the order-disorder transition temperature, limiting the applications of these materials, Elastic recovery of the XPX materials following seven cycles of tensile deformation is correlated with the fraction of X in the heptablock. copolymer, and the residual strain approaches that of CPC when the fraction of hard blocks f(X) <= 0.39.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.subject.enPOLYOLEFIN COMPOSITES
dc.subject.enDEFORMATION-BEHAVIOR
dc.subject.enABC TRIBLOCK COPOLYMERS
dc.subject.enSEMICRYSTALLINE BLOCK-COPOLYMERS
dc.subject.enORDER-DISORDER TRANSITION
dc.subject.enDIBLOCK COPOLYMERS
dc.subject.enMECHANICAL-PROPERTIES
dc.subject.enCATALYTIC-HYDROGENATION
dc.subject.enCYLINDRICAL MORPHOLOGY
dc.subject.enRUBBERY
dc.title.enSynthesis and Characterization of Elastomeric Heptablock Terpolymers Structured by Crystallization
dc.typeArticle de revue
dc.identifier.doi10.1021/ma100347k
dc.subject.halChimie/Polymères
bordeaux.journalMacromolecules
bordeaux.page5295-5305
bordeaux.volume43
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue12
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-00679987
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00679987v1
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Macromolecules&amp;rft.date=2010&amp;rft.volume=43&amp;rft.issue=12&amp;rft.spage=5295-5305&amp;rft.epage=5295-5305&amp;rft.eissn=0024-9297&amp;rft.issn=0024-9297&amp;rft.au=ALFONSO,%20C.%20Guillermo&amp;FLEURY,%20Guillaume&amp;CHAFFIN,%20Kimberly%20A.&amp;BATES,%20Frank%20S.&amp;rft.genre=article


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