Length-scale dependent relaxation shear modulus and viscoelastic hydrodynamic interactions in polymer liquids

A N Semenov1, J Farago, H Meyer

  • 1Institut Charles Sadron, CNRS-UPR 22, 23 rue du Loess, BP 84047, 67034 Strasbourg Cedex 2, France.

Summary

This study presents a quantitative theory for polymer hydrodynamic interactions, revealing they persist at large distances and are independent of molecular mass in pre-Rouse regimes. Viscoelastic effects significantly influence these interactions, leading to unique transient behaviors.

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