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Multiple melting endotherms in isothermally melt-crystallized poly(butylene terephthalate)

dc.contributor.authorKim, Hong Gyunen_US
dc.contributor.authorRobertson, Richard E.en_US
dc.date.accessioned2006-04-28T18:21:03Z
dc.date.available2006-04-28T18:21:03Z
dc.date.issued1998-07-30en_US
dc.identifier.citationKim, Hong Gyun; Robertson, Richard E. (1998)."Multiple melting endotherms in isothermally melt-crystallized poly(butylene terephthalate)." Journal of Polymer Science Part B: Polymer Physics 36(10): 1757-1767. <http://hdl.handle.net/2027.42/38877>en_US
dc.identifier.issn0887-6266en_US
dc.identifier.issn1099-0488en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38877
dc.description.abstractThe melting behavior of poly(butylene terephthalate) crystallized isothermally for various times was examined using differential scanning calorimetry. After short crystallization times, the DSC analysis gave two melting peaks, but after longer times, the analysis gave three peaks. The latter triplet of DSC peaks can be denoted as low, middle, and high, starting with the lowest temperature endotherm. The DSC peaks were simulated using a measured recrystallization rate and behavior for PBT and an assumed initial melting point distribution. The low and middle peaks represent the original melting peaks arising from isothermal crystallization. The high melting peak arises from recrystallization during the DSC heating scan. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1757–1767, 1998en_US
dc.format.extent253267 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.titleMultiple melting endotherms in isothermally melt-crystallized poly(butylene terephthalate)en_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.affiliationumMacromolecular Science & Engineering Center and Department of Materials Science & Engineering, 2300 Hayward St., 2014 H.H. Dow Bldg., The University of Michigan, Ann Arbor, Michigan 48109-2136en_US
dc.contributor.affiliationumMacromolecular Science & Engineering Center and Department of Materials Science & Engineering, 2300 Hayward St., 2014 H.H. Dow Bldg., The University of Michigan, Ann Arbor, Michigan 48109-2136 ; Macromolecular Science & Engineering Center and Department of Materials Science & Engineering, 2300 Hayward St., 2014 H.H. Dow Bldg., The University of Michigan, Ann Arbor, Michigan 48109-2136en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38877/1/17_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1099-0488(19980730)36:10<1757::AID-POLB17>3.0.CO;2-8en_US
dc.identifier.sourceJournal of Polymer Science Part B: Polymer Physicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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