Polymer Networks


In a second study [2] we highlight the very special properties
of networks of thermally fluctuating stiff polymers. As
compared to their purely mechanical counterparts, it is shown
that these thermal networks have a qualitatively different
elastic response. By accounting for the entropic origin of
the single-polymer elasticity, the networks acquire a strong
susceptibility to polydispersity and structural randomness that
is completely absent in athermal models.
In extensive numerical studies we systematically vary the
architecture of the networks and identify a wealth of phenomena
that clearly show the strong dependence of the emergent
macroscopic moduli on the underlying mesoscopic network
structure. In particular, we highlight the importance of the
full polymer length that to a large extent controls the elastic
response of the network, surprisingly, even in parameter regions
where it does not enter the macroscopic moduli explicitly. We
provide theoretical scaling arguments to relate the observed
macroscopic elasticity to the physical mechanisms on the
microscopic and the mesoscopic scale.
Literature:
-
C. Heussinger and
E. Frey,
Floppy Modes and Nonaffine Deformations in Random Fiber Networks,
Phys. Rev. Lett. 97, 105501 (2006) -
C. Heussinger and
E. Frey,
Stiff Polymers, Foams and Fiber Networks,
Phys. Rev. Lett. 96, 017802 (2006) [arXiv:cond-mat/0503359] -
C. Heussinger and
E. Frey,
The Role of Architecture in the Elastic Response of Semiflexible Polymer and Fiber Networks,
[arXiv:cond-mat/0512557]