An equation, based on thermodynamic considerations to relate the glass transition temperature, T g , to compositional variation of a polymer system, is adapted in this article for modeling the T g vs. fractional conversion ( x) relationship of reactive thermosetting systems. Agreement between the ad
Glass transition temperature versus conversion relationships for thermosetting polymers
✍ Scribed by J. P. Pascault; R. J. J. Williams
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 564 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0887-6266
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✦ Synopsis
Abstract
Owing to enthalpy relaxation, values of the glass transition temperature (T~g~) for partially reacted polymers may depend on the thermal history of samples and the heating rate used for measurements. Use of theoretical relations between T~g~ 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 T~g~ versus x. An extension of Couchman's approach for the expression of the compositional variation of T~g~ 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.
📜 SIMILAR VOLUMES
A single specimen of an epoxy/amine thermoset-glass fiber composite was examined, using a freely oscillating torsion pendulum operating at Ç 1 Hz, for different conversions (as measured by T g ) from T g 0 Å 0ЊC to T gϱ Å 184ЊC during cooling and heating temperature scans. T g was increased for succ