Abstract
Finite shear elasticity has been identified in the liquid state. The study is expanded to a van der Waal's molecular glass-former, o-terphenyl, and to an ordinary polymer melt, polybutylacrylate, as a function of their molecular weight. These fluids exhibit shear elasticity at the sub-millimetre scale and far above any phase transition. This macroscopic property challenges the conventional terminal relaxation modes (α-process or terminal viscoelastic times (reptation)) in terms of individual molecular process.
Acknowledgements
The authors are grateful to the Veeco Society for providing high resolution AFM photographs of the alumina substrates.