Dynamics of ring polymer melts: Memory function approach

Fuente: arXiv
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Main Authors: Fatkullin, Nail, Mattea, Carlos, Lindt, Kevin, Stapf, Siegfried, Kruteva, Margarita
Format: Preprint
Published: 2026
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author Fatkullin, Nail
Mattea, Carlos
Lindt, Kevin
Stapf, Siegfried
Kruteva, Margarita
author_facet Fatkullin, Nail
Mattea, Carlos
Lindt, Kevin
Stapf, Siegfried
Kruteva, Margarita
contents We investigated the static and dynamic properties of a Rouse ring polymer modified by introducing an effective, spherically symmetric, attractive potential of entropic nature and a memory function describing the effect of dynamic entanglement. Renormalized Rouse formalism is used to approximate the time dependence of the memory matrix. The results obtained are in good agreement with existing experimental data and the results of computer simulations of ring polymer ring with , , where N_e is the number of Kuhn segments in linear polymer melts between neighboring entanglements and , the number of Kuhn segments. For large molecular weights, a refined self-consistent approximation is proposed to describe the time dependence of the memory function. It is shown that this approximation allows us to describe an exponential decrease in the self-diffusion coefficient with molecular weight of the rings, i.e., the effect of dynamic localization.
format Preprint
id arxiv_https___arxiv_org_abs_2605_26905
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Dynamics of ring polymer melts: Memory function approach
Fatkullin, Nail
Mattea, Carlos
Lindt, Kevin
Stapf, Siegfried
Kruteva, Margarita
Soft Condensed Matter
We investigated the static and dynamic properties of a Rouse ring polymer modified by introducing an effective, spherically symmetric, attractive potential of entropic nature and a memory function describing the effect of dynamic entanglement. Renormalized Rouse formalism is used to approximate the time dependence of the memory matrix. The results obtained are in good agreement with existing experimental data and the results of computer simulations of ring polymer ring with , , where N_e is the number of Kuhn segments in linear polymer melts between neighboring entanglements and , the number of Kuhn segments. For large molecular weights, a refined self-consistent approximation is proposed to describe the time dependence of the memory function. It is shown that this approximation allows us to describe an exponential decrease in the self-diffusion coefficient with molecular weight of the rings, i.e., the effect of dynamic localization.
title Dynamics of ring polymer melts: Memory function approach
topic Soft Condensed Matter
url https://arxiv.org/abs/2605.26905