Herewith we discuss a new model for thermoset polymers that follow the autocatalytic curing kinetics. This model is proposed upon investigation of the crosslinking reaction of 2,2 0 -Bis(4-cyanatophenyl)isopropylidene (BACy), under isothermal conditions over a range of temperatures between 180 C and
An improved kinetic model for the autocatalytic curing of styrene-based thermoset resins
โ Scribed by P. W. K. Lam; H. P. Plaumann; T. Tran
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 613 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
The cure behavior of styrene-based thermosets such as orthophthalic polyester, isophthalic polyester, and vinyl ester resins is characterized using both isothermal and dynamic differential scanning calorimetry ( DSC) techniques. In the conventional autocatalyzed kinetic model, it is assumed that the isothermal cure reaction of a thermoset goes to completion, which usually leads to a poor fit with the DSC kinetic data. It appears from the conversion-time profiles that the cure reaction reached a plateau value (a,) less than unity. This is not unexpected, as the molecular mobility of the resin system decreases as the network cures. In this work, we have refined the model to remove this restrictive acsumption by taking the total ultimate conversion (a,) into account in the computation. This improved model permits us a better prediction of the course of the cure reaction of the styrene-based thermosets under isothermal and dynamic conditions. In addition, the cure kinetics of the three thermoset resins are studied and compared on the basis of several kinetic parameters including conversion, cure rate, reaction rate constant, heat of cure reaction, half-life, and Arrhenius parameters. The reactivity of these resins when arranged in ascending order is found to be: vinyl ester < orthophthalic polyester < isoththalic polyester.
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