The effect of a characteristic dimension of a glassy polymeric specimen on the kinetic mechanism controlling unidirectional absorption of organic vapors and liquids in glassy polymers is demonstrated by comparing n-alkane absorption experiments in microspheres, spheres, films, and sheets of polystyrene. Absorption in submicron microspheres is controlled by Fickian diffusion whereas, under otherwise identical boundary conditions, films (ca. 75μm thick) and spheres (ca. 184 μm in diameter) sorb according to Case II absorption kinetics. Thinner films (35 μm thick) sorb by Super Case II kinetics and relatively thick sheets (2000 μm thick) sorb initially by Case II kinetics but, at long times, diffusion through the outer swollen region contributes significantly to the overall resistance to mass transfer and the rate of absorption decreases progressively with time. p]The rather short experimental times, afforded by the exceedingly small mean diameter of the narrowly distributed microsphere powder sample, permitted convenient characterization of the effects of preswelling, sorption-desorption cycling, and annealing on the kinetics and apparent equilibria of sorption. History effects were quite dramatic and were related to glassy state relaxations initiated by the various thermal and swelling histories imposed upon the glassy microspheres. p]Prediction of sorption and permeation behavior in membranes, from kinetic and equilibrium parameters determined experimentally on film and powder samples, requires explicit recognition of these dimensional and history effects. These effects do not appear to be related to any special properties of this polymer-penetrant system.
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