2008 APS March Meeting
Volume 53, Number 2
Monday–Friday, March 10–14, 2008;
New Orleans, Louisiana
Session H3: Polymer Physics Prize
8:00 AM–11:00 AM,
Tuesday, March 11, 2008
Morial Convention Center
Room: RO2 - RO3
Sponsoring
Unit:
DPOLY
Chair: Mark Ediger, University of Wisconsin-Madison
Abstract ID: BAPS.2008.MAR.H3.1
Abstract: H3.00001 : Polymer Prize Talk: Segmental Dynamics in Polymers : From Cold Melts to Aging and Stressed Glasses
8:00 AM–8:36 AM
Preview Abstract
Abstract
Author:
Kenneth Schweizer
(University of Illinois @ Urbana-Champaign)
Polymers are excellent glass formers. In the cold molten state
they exhibit
chemically-specific and strongly non-Arrenhius segmental
relaxation which
sets the time scale for the generic chain scale dynamics. In the
amorphous
solid or plastic state the temperature dependence of the alpha
relaxation
time changes, physical aging emerges, and a rich mechanical
response occurs
characterized by the dynamic yielding, strain softening and
strain hardening
processes. We have developed a statistical mechanical theory of
activated
segmental relaxation in cold melts by combining and extending
methods of
mode coupling, dynamic density functional and activated hopping
theories.
The approach is built on the concept of a confining
nonequilibrium free
energy which quantifies local dynamical constraints and the
barrier hopping
process. The localizing consequences of interchain caging forces are
quantified by the amplitude of nanometer scale density fluctuations
(compressibility) and backbone stiffness. Predictions for the
kinetic glass
and dynamic crossover temperatures, dynamic fragility, and thermal
dependence of the segmental relaxation time are consistent with
experiments.
The theory has been generalized to treat alpha relaxation,
physical aging,
and nonlinear mechanical properties in the glass. The structural
component
of density fluctuations become (partially) frozen resulting in a
crossover
to Arrenhius relaxation. Physical aging is modeled based on a
kinetic
equation for collective density fluctuations. At intermediate
time scales
the relaxation time (shear modulus) grows as a power law
(logarithmic)
function of aging time with a temperature dependent exponent.
Applied stress
weakens dynamical constraints thereby accelerating relaxation and
softening
the elastic modulus. A constitutive equation has been constructed
from which
the temperature dependent dynamic yielding and mechanical
response under
constant strain rate, constant stress (creep), and other modes of
deformation can be calculated. This work was done in
collaboration with Drs.
Kang Chen and Erica J. Saltzman.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2008.MAR.H3.1