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Gas chromatographic measurements of infinite dilution diffusion coefficients of volatile liquids in amorphous polymers at elevated temperatures
Author(s) -
Hu David S.,
Han Chang Dae,
Stiel Leonard I.
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.1987.070330222
Subject(s) - inverse gas chromatography , polymer , polystyrene , dilution , glass transition , diffusion , volume (thermodynamics) , ethylbenzene , analytical chemistry (journal) , amorphous solid , benzene , materials science , toluene , van deemter equation , thermodynamics , vinyl acetate , chemistry , polymer chemistry , chromatography , organic chemistry , high performance liquid chromatography , composite material , physics , copolymer
Measurements were made of infinite dilution diffusion coefficients of volatile liquids in amorphous polymers at elevated temperatures, using inverse gas chromatography. The liquids used were benzene, toluene, ethylbenzene, and n ‐decane. The polymers used were polystyrene and poly(vinyl acetate), and temperatures ranged from 30°C to 120°C above the glass transition temperatures of the polymers. Packed chromatographic columns were used to obtain data of the variation of the plate height with the average gas velocity, which was then used to determine diffusion coefficients with the aid of the van Deemter equation. In the present investigation, we have used different sizes of glass beads (0.3, 0.5, 0.6, and 1.0 mm in diameter), depending on the system temperature and the polymer/solute pair chosen. An attempt was made to correlate on the diffusion coefficient D measured at various temperatures T , using in D ζ as ordinate and 1/[( K 22 + T − T g 2 )/ T c ] (hereafter referred to as the reciprocal of reduced free volume temperature, 1/ T RF ) as abscissa, in which ζ = M 1/2 / T 1/2 cV 1/3 c , M being the molecular weight, T c the critical temperature, and V c the critical volume of the solute, K 22 is a free volume parameter of the polymer, and T g 2 is the glass transition temperature of the polymer. It has been found that such plots give rise to two linear regions having different slopes, separated by a critical value of 1/ T RF . The critical value of 1/ T RF is found to be insensitive to the type of solute and the type of polymer used. We have concluded that the infinite dilution diffusion coefficient of volatile liquids in amorphous polymers is controlled predominatly by the free volume of polymer above a critical value of 1/ T RF , but energy effects are significant below the critical value of this parameter. In order to apply the generalized relationships in conjunction with gas chromatographic measurements, the results of this study indicate that, for values of 1/ T RF larger than a critical value, which is approximately 4.8, the following expression, In D ζ = α + b / T RF , may be used to predict infinite dilution diffusion coefficients of volatile liquids in amorpous polymers at elevated temperatures, in which α is a constant, independent of the type of solute, and b is approximately a constant for a given polymer in the free volume region, independent of the type of solute. More experimental studies are needed, particularly for temperatures higher than those reported in this study, to corroborate and/or extend the correlations presented here.