Dynamical Monte Carlo Study of Equilibrium Polymers : Static Properties
J.P. Wittmer, A. Milchev, M.E. Cates

TL;DR
This study uses advanced Dynamical Monte Carlo simulations to analyze static properties of equilibrium polymers, confirming theoretical predictions about chain length scaling and distribution in various density regimes.
Contribution
Introduces a novel efficient algorithm for simulating large equilibrium polymer systems, enabling detailed static and dynamic property analysis across a wide density range.
Findings
Mean-chain length scales with density and scission energy as predicted.
Chain length distribution follows Schulz-Zimm form in dilute limit.
Accurate determination of the self-avoiding walk susceptibility exponent γ ≈ 1.165.
Abstract
We report results of extensive Dynamical Monte Carlo investigations on self-assembled Equilibrium Polymers (EP) without loops in good solvent. (This is thought to provide a good model of giant surfactant micelles.) Using a novel algorithm we are able to describe efficiently both static and dynamic properties of systems in which the mean chain length is effectively comparable to that of laboratory experiments (up to 5000 monomers, even at high polymer densities). We sample up to scission energies of over nearly three orders of magnitude in monomer density , and present a detailed crossover study ranging from swollen EP chains in the dilute regime up to dense molten systems. Confirming recent theoretical predictions, the mean-chain length is found to scale as where the exponents approach $\alpha_d=\delta_d=1/(1+\gamma)…
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