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Rouse Mode Analysis of Relaxation in Polymer Blends
Author(s) -
Li Wei,
Cao XueZheng,
Merlitz Holger,
Wu ChenXu
Publication year - 2021
Publication title -
macromolecular theory and simulations
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.37
H-Index - 56
eISSN - 1521-3919
pISSN - 1022-1344
DOI - 10.1002/mats.202000084
Subject(s) - relaxation (psychology) , polymer , rheology , component (thermodynamics) , superposition principle , materials science , polymer blend , monomer , length scale , molecular dynamics , thermodynamics , chemical physics , chemistry , polymer chemistry , computational chemistry , composite material , physics , copolymer , mechanics , psychology , social psychology , quantum mechanics
The relaxation spectra of the components in polymer blends determine the dynamic mechanical properties of the corresponding composite materials, which, in thermo‐rheological studies, show a delicate dependence on their chemical and physical properties as well as its bulk composition. A molecular dynamics simulation based Rouse mode analysis is performed to detect the relaxation spectra of the component chains on all length scales ranging from one monomer to the whole chain size, indicating that the bulk composition dominates the relaxation dynamics of the components in miscible polymer blends. The relaxation of component chains accelerates on all length scales as increasing the free volume available to monomers to move, with the dependence of mobility shift on composition being quantified by a Williams–Landel–Ferry like function governing the time‐composition superposition. Role of the chain connectivity induced self‐concentration effect on chain relaxation in polymer blends is discussed and proved to be limited, which leads to a visible but subtle length‐scale dependent rheological complexity as the composition is varied.