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Effect of vinylacetate content on crystallinity and second‐order transitions in ethylene—vinylacetate copolymers
Author(s) -
Brogly M.,
Nardin M.,
Schultz J.
Publication year - 1997
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/(sici)1097-4628(19970606)64:10<1903::aid-app4>3.0.co;2-m
Subject(s) - comonomer , crystallinity , copolymer , differential scanning calorimetry , materials science , amorphous solid , crystallization , polymer chemistry , polyethylene , phase (matter) , ethylene , chemical engineering , polymer , thermodynamics , crystallography , organic chemistry , composite material , chemistry , physics , catalysis , engineering
Thermal characteristics of ethylene—vinylacetate (EVA) copolymers having vinylacetate contents ranging from 5 to 40 w/w % are studied by differential scanning calorimetry. It is first shown that EVA copolymers having a vinylacetate content lower than 30 w/w % obey the Flory and Burfield theories of copolymer crystallisation. The minimum sequence length of CH 2 ethylenic entities required to participate in a crystalline lamella is also deduced. One can conclude that EVA copolymers represent cases of “total exclusion” of the noncrystallizable comonomer. Moreover, it is observed that when the vinylacetate content is increased, the relative quantity of polyethylene amorphous phase increases and the degree of crystallinity decreases; whereas the β transition temperature of a characteristic‐oriented amorphous phase is kept constant. A phase model of ethylene‐vinylacetate copolymers, based on an enrichment process of the interlamellar amorphous phase by polyethylene segments originating from the crystalline phase, at increasing vinylacetate content, is proposed. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 64: 1903–1912, 1997