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Gas permeation in miscible homopolymer–copolymer blends. I. Poly(methyl methacrylate) and styrene/acrylonitrile copolymers
Author(s) -
Chiou J. S.,
Paul D. R.
Publication year - 1987
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.1987.070340314
Subject(s) - copolymer , acrylonitrile , materials science , permeation , polymer blend , polymer chemistry , sorption , styrene , methyl methacrylate , hildebrand solubility parameter , miscibility , solubility , polymer , phase (matter) , polystyrene , flory–huggins solution theory , chemical engineering , composite material , membrane , chemistry , organic chemistry , adsorption , engineering , biochemistry
Gas transport properties in homogeneous blends of PMMA with each of two SAN random copolymers, containing 13.5 and 28% by weight of acrylonitrile respectively, have been measured at 35°C for He, H 2 , O 2 , N 2 , Ar, CH 4 , and CO 2 . For all cases, the permeability and diffusion coefficients are higher than that expected from the semilogarthmic additivity rule. On the other hand, the solubility coefficients and the ideal gas separation factors follow this rule well. These results for PMMA/SAN blends differ from those observed recently for other miscible blend systems; however, they agree well with recent theories proposed to describe gas sorption and permeation behavior in polymer mixtures. The composition dependence of gas transport properties observed in PMMA/SAN blends is attributed to the very weak net interactions between PMMA and SAN produced by repulsions between styrene and acrylonitrile units in the SAN random copolymers. Gas transport properties in phase‐separated PMMA/SAN blends have also been studied. The phase‐separated blends show sorption and permeation properties very similar to the corresponding homogeneous blends which can be explained by an isotropic, interconnected, two‐phase model proposed by Kraus and Rollmann. Gas permeabilities for the solution cast PMMA films used here are compared with melt‐extruded specimens used previously, and the differences are attributed to molecular orientation.