Relating Chain Conformations to Extensional Stress In Entangled Polymer Melts
arXiv:1806.09509 · doi:10.1103/PhysRevLett.121.047801
Abstract
Nonlinear extensional flows are common in polymer processing but remain challenging theoretically because dramatic stretching of chains deforms the entanglement network far from equilibrium. Here, we present coarse-grained simulations of extensional flows in entangled polymer melts for Rouse-Weissenberg numbers - and Hencky strains . Simulations reproduce experimental trends in extensional viscosity with time, rate and molecular weight. Studies of molecular structure reveal an elongation and thinning of the confining tube with increasing . The rising stress is quantitatively consistent with the decreasing entropy of chains at the equilibrium entanglement length. Molecular weight dependent trends in viscosity are related to a crossover from the Newtonian limit to a high rate limit that scales differently with chain length.
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- Comment on: "Relating Chain Conformations to Extensional Stress in Entangled Polymer Melts"
- O'Connor, Alvarez, and Robbins Reply to Xu et al. (arXiv:1808.05390)
- Identifying the Threshold Chain Length for Stress Overshoot in Ring-Linear Polymer Blends under Uniaxial Elongation: The Role of Multiple Threading
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