Angular correlations in dense solutions and melts of flexible polymer chains are investigated with respect to the distance r between the bonds by comparing quantitative predictions of perturbation calculations with numerical data obtained by Monte Carlo simulation of the bond-fluctuation model. We consider both monodisperse systems and grand-canonical (Flory-distributed) equilibrium polymers. Density effects are discussed as well as finite chain length corrections. The intrachain bond-bond correlation function P(r) is shown to decay as P(r)∼1/r3 for \xi \ll r \ll \r^* with ξ being the screening length of the density fluctuations and r∗∼N1/3 a novel length scale increasing slowly with (mean) chain length N.
@article{arxiv.0912.3340,
title = {Distance dependence of angular correlations in dense polymer solutions},
author = {J. P. Wittmer and A. Johner and S. P. Obukhov and H. Meyer and A. Cavallo and J. Baschnagel},
journal= {arXiv preprint arXiv:0912.3340},
year = {2015}
}
Comments
17 pages, 5 figures, accepted for publication at Macromolecules