Presented to the Division of High Polymer Physics, American Physical Society Meeting, Atlanta, Georgia, April 1, 1976. Work supported by the U.S. Energy Research and Development Administration.
Domain structure and time-dependent properties of a crosslinked urethane elastomer†
Article first published online: 9 MAR 2003
Copyright © 1977 John Wiley & Sons, Inc.
Journal of Applied Polymer Science
Volume 21, Issue 9, pages 2489–2503, September 1977
How to Cite
Lagasse, R. R. (1977), Domain structure and time-dependent properties of a crosslinked urethane elastomer. J. Appl. Polym. Sci., 21: 2489–2503. doi: 10.1002/app.1977.070210917
- Issue published online: 9 MAR 2003
- Article first published online: 9 MAR 2003
- Manuscript Revised: 2 JUL 1976
- Manuscript Received: 3 MAY 1976
The morphology of a chemically crosslinked urethane elastomer is correlated with its time-dependent mechanical properties. Evaluation of this amorphous elastomer by electron microscopy and small-angle x-ray scattering reveals that incompatible chain segments cluster into separate microphases having a periodicity in electron density of about 90 Å. This observed domain structure is similar to that seen previously in uncrosslinked, thermoplastic urethane elastomers. As in earlier studies on such linear system, thermal pretreatment of the crosslinked elastomer causes a time-dependent change in its room temperature modulus. However, the magnitude of this modulus change (about 20%) is generally less than observed previously with the linear systems. Another contrast with previous findings is that this time-dependent phenomenon is apparently not caused by thermally activated changes in microphase segregation. Rather, the observed time dependence in modulus is believed to be caused by molecular relaxation resulting in densification of amorphous packing within the hard-segment domains. The validity of this proposed mechanism is supported by differential scanning calorimetry experiments showing evidence of enthalpy relaxation during room-temperature aging of the elastomer. This relaxation is qualitatively similar to that observed previously during sub-Tg annealing of single-phase glassy polymers.