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Effect of chain architecture on biaxial orientation and oxygen permeability of polypropylene film
Author(s) -
Dias P.,
Lin Y. J.,
Hiltner A.,
Baer E.,
Chen H. Y.,
Chum S. P.
Publication year - 2007
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/app.27197
Subject(s) - materials science , crystallinity , oxygen permeability , tacticity , amorphous solid , polymer , copolymer , composite material , polypropylene , permeability (electromagnetism) , polymer chemistry , oxygen , polymerization , crystallography , membrane , organic chemistry , chemistry , biochemistry
Films of two isotactic propylene homopolymers prepared with different catalysts and a propylene/ethylene copolymer were biaxially oriented under conditions of temperature and strain rate that were similar to those encountered in a commercial film process. The draw temperature was varied in the range between the onset of melting and the peak melting temperature. It was found that the stress response during stretching depended on the residual crystallinity in the same way for all three polymers. Biaxial orientation reduced the oxygen permeability of the oriented films, however, the reduction did not correlate with the amount of orientation as measured by birefringence, with the fraction of amorphous phase as determined by density, or with free volume hole size as determined by PALS. Rather, the decrease in permeability was attributed to reduced mobility of amorphous tie molecules. A single one‐to‐one correlation between the oxygen permeability and the intensity of the dynamic mechanical β‐relaxation was demonstrated for all the polymers used in the study. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008