Abstract

Angular correlations in dense solutions and melts of flexible polymer chains are investigated with respect to the distance rr 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)P(r) is shown to decay as P(r)∼1/r3P(r) \sim 1/r^3 for $ξ\ll r \ll \r^*$ with ξξ being the screening length of the density fluctuations and r∗∼N1/3r^* \sim N^{1/3} a novel length scale increasing slowly with (mean) chain length NN.

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