ISSN:
0098-1273
Keywords:
Physics
;
Polymer and Materials Science
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
,
Physics
Notes:
The time - temperature superposition principle is well-established for linear viscoelastic properties of polymer systems. It is generally supposed that the same principle carries over into nonlinear phenomena, such as the relationship between viscosity η and shear rate \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document}. Guided by this principle and the forms of various molecular theories, one would expect that η - \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document} data on the same polymer at different temperatures would superimpose when plotted as η/η0 versus \documentclass{article}\pagestyle{empty}\begin{document}$ \dot \gamma $\end{document}η0/ρT, η0 being the limiting viscosity at low shear rates, ρ the polymer density, and T the absolute temperature. Data on polystyrene melts, obtained in a plate-cone viscometer, appear systematically to violate this principle in the range 140-190°. Such anomalies are absent in concentrated solutions of polystyrene. The trends are similar to those reported by Plazek in the steady-state compliance of polystyrene melts near Tg, but they appear to persist to higher temperatures than the compliance anomaly.
Additional Material:
11 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/pol.1974.180120904
