Abstract
The glass transition temperatures, Tg, of polystyrene, poly (vinyl chloride) and poly(methyI methacrylate) have been determined from gas chromatographic measurements using n‐hexane, n‐heptane, meta‐xylene and para‐xylene solvents. The glass transition temperatures were detected on the z‐shaped retention diagrams which were produced from the plot of the logarithm of the specific retention volumes of the above‐mentioned solvents against the reciprocal of temperature, i.e. log V vs. 1/T. The glass transition temperature is specified by the temperature where the slope of log V vs. 1/T changes abruptly. The observed glass transition temperature of polystyrene produced by this technique was found to be in good agreement with those produced by other techniques such as the differential scanning colorimeter.
The industrial importance of the glass transition temperature, T~g~, might be due to the dramatic changes in the physical properties of the polymer, such as hardness and elasticity, which take place in the vicinity of this temperature. However, perfectly crystalline polymers do not exhibit glass transitions, because their chains are incorporated in regions of three‐dimensional order, called crystallites. Completely amorphous polymers and semi‐crystalline polymers usually exhibit both glass transition and melting.