Abstract

In this communication, we propose a different approach for analyzing linear viscoelastic relaxation data that is more faithful to the underlying physics and naturally accommodates the thermorheological complexity that is observed in glass-forming polymers. Specifically, the linear viscoelastic behavior was evaluated for a diglycidyl ether of bisphenol-A epoxy cured with 4,4′-methylenedianaline with a glass transition temperature (Tg) of 101.5 °C. The dynamic storage and loss moduli were measured from 10–2 to 101.7 Hz for 19 temperatures between 90 and 180 °C. The experimental window was extended by two orders of magnitude using stress relaxation experiments for temperatures between 90 and 112.5 °C. The G′ and G″responses for this single-phase polymer are thermorheologically complex, thus precluding the construction of master curves via time–temperature superposition. The traditional method of determining the relaxation spectrum implicitly assumes a constant spectral density where the spectral strength cha...

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