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Non‐Isothermal Crystallization Kinetics of an Ethylene‐Vinyl‐Acetate. II. Time‐Temperature‐Crystallinity‐Superposition
Author(s) -
Carotenuto Claudia,
Grassia Luigi,
Paduano Liana P.,
Minale Mario
Publication year - 2019
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.25242
Subject(s) - crystallinity , materials science , ethylene vinyl acetate , crystallization , time–temperature superposition , viscoelasticity , vinyl acetate , ethylene , isothermal process , polymer chemistry , relaxation (psychology) , chemical engineering , thermodynamics , copolymer , polymer , composite material , organic chemistry , chemistry , catalysis , physics , engineering , psychology , social psychology
Ethylene vinyl acetate (EVA) is a random copolymer of ethylene and varying amounts of vinyl acetate that interfere with poly‐ethylene chain packing reducing crystallinity, thus improving transparency and lowering the melting temperature to 40°C–60°C. The material viscoelastic properties in its working conditions may thus depend on the crystallinity degree. The crystallization process is here rheologically studied in non‐isothermal conditions and the frequency spectra are measured at different temperatures to investigate the viscoelasticity of EVA. Coupling the crystallization kinetics and the viscoelastic spectra at different temperatures, that is, at different degree of crystallinity, we here determine two independent shift factors, one for the time‐crystallinity shift, the other for the time‐temperature shift, so to propose a new time‐temperature‐crystallinity‐superposition to reconcile all the data on a single master curve. In this way, the experimentally observable frequency range has been widened significantly so to detect all the relaxation times of the material from the shortest to the largest ones. POLYM. ENG. SCI., 59:2550–2556, 2019. © 2019 Society of Plastics Engineers
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