English

Self-similar chain conformations in polymer gels

Soft Condensed Matter 2009-10-31 v1 Materials Science

Abstract

We use molecular dynamics simulations to study the swelling of randomly end-cross-linked polymer networks in good solvent conditions. We find that the equilibrium degree of swelling saturates at Q_eq = N_e**(3/5) for mean strand lengths N_s exceeding the melt entanglement length N_e. The internal structure of the network strands in the swollen state is characterized by a new exponent nu=0.72. Our findings are in contradiction to de Gennes' c*-theorem, which predicts Q_eq proportional N_s**(4/5) and nu=0.588. We present a simple Flory argument for a self-similar structure of mutually interpenetrating network strands, which yields nu=7/10 and otherwise recovers the classical Flory-Rehner theory. In particular, Q_eq = N_e**(3/5), if N_e is used as effective strand length.

Keywords

Cite

@article{arxiv.cond-mat/9909453,
  title  = {Self-similar chain conformations in polymer gels},
  author = {Mathias Puetz and Ralf Everaers and Kurt Kremer},
  journal= {arXiv preprint arXiv:cond-mat/9909453},
  year   = {2009}
}

Comments

4 pages, RevTex, 3 Figures

R2 v1 2026-07-22T12:15:17.122Z