Dynamic Arrest in Polymer Melts: Competition between Packing and Intramolecular Barriers
arXiv:0809.5252 · doi:10.1103/PhysRevLett.101.255701
Abstract
We present molecular dynamics simulations of a simple model for polymer melts with intramolecular barriers. We investigate structural relaxation as a function of the barrier strength. Dynamic correlators can be consistently analyzed within the framework of the Mode Coupling Theory (MCT) of the glass transition. Control parameters are tuned in order to induce a competition between general packing effects and polymer-specific intramolecular barriers as mechanisms for dynamic arrest. This competition yields unusually large values of the so-called MCT exponent parameter and rationalize qualitatively different observations for simple bead-spring and realistic polymers. The systematic study of the effect of intramolecular barriers presented here also establishes a fundamental difference between the nature of the glass transition in polymers and in simple glass-formers.
4 pages, 3 figures, 2 tables
References in corpus (8)
- Liquid-glass transition of a fluid confined in a disordered porous matrix: A mode-coupling theory
- Confirmation of Anomalous Dynamical Arrest in attractive colloids: a molecular dynamics study
- Logarithmic Relaxation in Glass-Forming Systems
- Relaxation Scenarios in a Mixture of Large and Small Spheres: Dependence on the Size Disparity
- Anomalous Dynamic Arrest in a Mixture of Big and Small Particles
- Logarithmic Relaxation in a Colloidal System
- Structural and conformational dynamics of supercooled polymer melts: Insights from first-principles theory and simulations
- Atomic motions in the -region of glass-forming polymers: Molecular versus Mode Coupling Theory approach
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