Glass transition temperature versus conversion relationships for thermosetting polymers

作者：Jean‐Pierre Pascault, Roberto J. J. Williams · 发表于：Journal of Polymer Science Part B Polymer Physics · 年份：1990 · DOI：10.1002/polb.1990.090280107 · 被引用次数：440 · 研究领域：Polymer crystallization and properties、Thermal and Kinetic Analysis、Epoxy Resin Curing Processes

Abstract Owing to enthalpy relaxation, values of the glass transition temperature (Tg) for partially reacted polymers may depend on the thermal history of samples and the heating rate used for measurements. Use of theoretical relations between Tg and the extent of reaction (x) of a thermoset must take this fact into account. The original DiBenedetto equation has been reevaluated as a convenient constitutive equation for expressing Tg versus x. An extension of Couchman's approach for the expression of the compositional variation of Tg enabled us to derive the same functionality as given by the DiBenedetto equation. Thus, the DiBenedetto equation may be regarded as based on entropic considerations applied to a model of the thermosetting polymer consisting of a random mixture of a fully reacted network with the initial monomers in an amount which depends on the particular conversion level. These two equations have been applied with success to different diepoxy‐diamine copolymers.