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Polymer Sciences | ISSN: 2471-9935
October 02-03, 2017 Chicago, USA
3
rd
International Conference on
Polymer Science and Engineering
Discovery of static shear-elasticity in liquids & melts
Laurence Noirez, Patrick Baroni
and
Philipp Kahl
University Paris-Saclay, France
O
n the basis of a Maxwell gas model (1867), it has long been suspected that liquids and polymer melts exhibit (shear) elasticity at
sufficiently high solicitation frequencies (MHz or GHz) only. Recent experimental improvements indicate that liquids exhibit
also shear elasticity at very low frequency (0.1 to 10Hz). This finding is of utmost importance, since it means that liquids are no
fully viscous, but possess a weak but finite elastic threshold below which they are solids. The elastic property has been identified at
sub-millimeter scale, both on simple liquids and complex fluids (polymer melts, molecular glass formers, Van der Waals liquids,
ionic liquids, H-bond liquids) pointing out the generic characteristic of this neglected property that invalidates the single molecular
approach of the viscoelasticity. We present the first experiments identifying static shear elasticity in the bulk from unentangled to
entangled polymer melts. In particular, we show how the low frequency shear elasticity and the usual viscoelastic response are related.
The low frequency shear elasticity involves collective processes and has profound implications on how the melt flows, on flow and
surface instabilities, thermodynamics, fluidic transport mechanisms enables to foresee new effects as the cold production or the
spectacular conversion of a liquid melt in a strain-driven optical harmonic oscillator.
laurence.noirez@cea.frPolym Sci, 3:3
DOI: 10.4172/2471-9935-C1-003




