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Kinetics for the growth of rigid amorphous fraction in cyclic olefin copolymers (COC)

dc.citation.epage2191en_US
dc.citation.issue5en_US
dc.citation.spage2185en_US
dc.citation.volume42en_US
dc.citation.woscount8
dc.contributor.authorChu, PPJen_US
dc.contributor.authorHuang, WJen_US
dc.contributor.authorChang, FCen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:44:08Z
dc.date.available2014-12-08T15:44:08Z
dc.date.issued2001-03-01en_US
dc.description.abstractBoth linear William-Watts (WW) and non-linear Narayanaswamy-William-Watts (NWW) stretch relaxation satisfactorily described the time dependent rigid amorphous phase growth kinetic. The model is tested upon the completely amorphous cyclic olefin copolymers (COC, polynorbornene/polyethylene copolymer), where a large T-g variation is detected with annealing. Increase of the rigid amorphous fraction as reflected in the increase of T-g, is attributed to the growth of short range ordered phase due to the rigidity of the norbornene chain segment. The analysis shows the growth kinetic (represented by the retardation time, and the stretch exponent) that depends not only on the norbornene (NB) content but also on the NE microblock structure. The kinetics for the growth of the rigid amorphous domains follows a stretched exponential expression, similar to that given for polymer crystallization and physical aging. (C) 2000 Elsevier Science Ltd. All rights reserved.en_US
dc.identifier.issn0032-3861en_US
dc.identifier.journalPOLYMERen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/29796
dc.identifier.wosnumberWOS:000165572300043
dc.language.isoen_USen_US
dc.subjectdensificationen_US
dc.subjectkineticsen_US
dc.subjectcyclic olefin copolymersen_US
dc.titleKinetics for the growth of rigid amorphous fraction in cyclic olefin copolymers (COC)en_US
dc.typeArticleen_US

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