Specific volume of polysulfone as a function of temperature and pressure

Abstract

AbstractThe pressure–volume–temperature (PVT) properties of a commercial polysulfone derived from bisphenol A and 4,4′‐dichlorodiphenylsulfone are studied experimentally and theoretically in the temperature range 30–370°C and for pressures to 2000 kg/cm2. PVT surfaces are determined for an annealed glass, formed under zero pressure, and for the melt. Two glass‐transition lines must be distinguished: T(P) which is the intersection of the glass and melt PVT surfaces, and Tg(P), which is obtained by pressurizing the melt isothermally. The application of Ehrenfest‐type equations to these transitions are discussed. The Prigogine–Defay ratio r = ΔkΔCp/TV(Δα)2 at P = 0 is found to be equal to 0.95 (±20%), using ΔCp data determined on identical samples. The melt data is compared with the Simha–Somcynski hole theory, using the reducing parameters V* = 0.788 cm3/g, T* = 12,560°K, P* = 10,875 bar. The hole fraction appearing in the theory is found to be constant along T(P), but the glass PVT relationship cannot be reproduced by using the Simha–Somcynsky theory together with the assumption that the hole fraction remains constant in the glass. At P = 0 the hole fraction must be allowed to decrease with decreasing temperature, but at a slower rate than in the melt.