Copolymers of poly(ethylene terephthalate) (PET) containing 1–24% poly(diethylene glycol)terephthalate (PDEGT) were prepared and characterized by infrared spectra. The energy and entropy of activation for the thermal degradation were measured for these copolymers and for the PDEGT. These activation energies and energies and entropies were found to decrease steadily with increasing diethylene glycol content. From these measurements the mechanism of degradation of PDEGT was found to be different from that of PET. Fibers prepared from seven different copolymeric compositions were heat‐aged at 121°C and 204°C for 24 hr. From the changes observed in intrinsic viscosity, per cent ether, hydroxyl and carboxyl endgroups during heat aging it became apparent that the mechanisms for decomposition are operative below melt temperatures and can rapidly destroy such copolymers.
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William L. Hergenrother (1974) studied this question.
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