Measurements of velocity and attenuation of ultrasonic waves are carried out for polystyrene, polymethyl methacrylate, phenol resin, polyethylene, nylon 6 and other commercial resins in the temperature from -60°C to 90°C and at frequencies of 100 kc, 1.46 Mc, 4.38 Mc and 7.30 Mc. A correlation between sound velocity in the megacycle range and density is pointed out for glassy polymers. In the case of linear polymers, the temperature coefficient of ultrasonic velocity, β, exhibits a relatively abrupt change in the glass trasition region at the temperature T m , which is independent of frequency of sound agrees with the transition point associated with thermal expansion. The ratio of β to volume expansion coefficient α is found to be constant below and above T m for each polymer. These facts indicate that the change in β at T m should be ascribed to the temperature dependence of intermolecular free volume. For some polymers a change in β and a peak of loss factor are observed at lower temperatures.
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Wada et al. (1956) studied this question.
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