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New data are reported for the permeation of inert gases through polyethylene, polytetrafluoroethylene, and silicone and natural rubbers. Additional data are compiled from the literature. The relative solubilities of these gases are practically insensitive to chemical variations in the homopolymer. Hence variations in structure at the glass transition ( T g ) and melting ( T m ) temperatures that affect diffusion also unambiguously affect permcation. Consequently an equivalence results between permeation at a given temperature for different polymers and permeation at different temperatures for a given polymer. Although the diffusion coefficient changes continuously with temperature, the Arrhenius parameters D o and E d apparently change discontinuously at T g and T m . Their magnitudes and variations with atomic weight reach maxima at about T g . These data indicate a dependence of the classical correlation between D o and E d on polymer properties. A perturbed diameter for the permeant, specific for each polymer, is proposed for correlating the D o and E d data. This correlation makes the changes observed at T g and T m more perceptible.
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Lundstrom et al. (1974) studied this question.
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