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Gas transport in halogen‐containing aromatic polycarbonates
Author(s) -
Hellums M. W.,
Koros W. J.,
Husk G. R.,
Paul D. R.
Publication year - 1991
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.1991.070431103
Subject(s) - polycarbonate , solubility , glass transition , halogen , thermal diffusivity , polymer , polymer chemistry , bromine , materials science , selectivity , diffusion , chemistry , chemical engineering , organic chemistry , thermodynamics , alkyl , catalysis , physics , engineering
The gas permeability and permselectivity of a series of halogen‐containing polycarbonates are discussed in terms of the fundamental solubility and diffusivity factors. These materials have structural features that hinder interchain packing and intrachain rotational mobility. Both diffusion and solubility coefficients are higher in materials with higher fractional free volumes. Diffusivity selectivities tend to increase with increasing restriction of intrachain torsional mobility. The materials with four bromine atoms substituted on the phenyl rings ortho to the carbonate linkages display a significantly increased diffusivity selectivity relative to conventional polycarbonate. This improvement in the ability of the polymer matrix to discriminate between gas molecules of different sizes is due to a reduction in intrachain torsional mobility. The reduction in chain mobility is indicated by higher glass transition and higher sub‐ T g transition temperatures in the bromine‐substituted materials. The materials with hexafluoroisopropylidene moieties have high fractional free volumes and exhibit a very significant increase in permeability relative to conventional bisphenol‐A polycarbonate. The material with both the hexafluoro and the tetrabromo substitutions displays significant simultaneous increases in permeability and permselectivity relative to conventional polycarbonate.