Viscoelastic properties of marginal networks in a solvent

被引:6
|
作者
Dennison, M. [1 ]
Stark, H. [1 ]
机构
[1] Tech Univ Berlin, Inst Theoret Phys, Hardenbergstr 36, D-10623 Berlin, Germany
关键词
MULTIPARTICLE COLLISION DYNAMICS; SEMIFLEXIBLE POLYMER NETWORKS; MICROSCOPIC VISCOELASTICITY; THERMAL FLUCTUATIONS; ELASTIC NETWORKS; ACTIN SOLUTIONS; DIMENSIONS; PERCOLATION; SIMULATION; HYDROGELS;
D O I
10.1103/PhysRevE.93.022605
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
Polymer networks at the margins of mechanical stability are known to be highly sensitive to applied forces and fields and to exhibit an anomalously large resistance to deformation. In this paper, we study the effects of hydrodynamic interactions on the behavior of marginal networks using a hybrid molecular dynamics and multiparticle collision dynamics simulation technique. We examine how the filament and solvent properties affect the response of marginal networks to shear. We find that the stiffening of the network shows a stronger dependence on the shear frequency when hydrodynamic interactions are present than when they are not. The network shear modulus scales as G' similar to omega(alpha c), with a critical stiffening exponent alpha(c) that can be controlled by varying the relative concentrations of the network and the solvent. Our results show that this arises due to the solvent aiding the relaxation of the network and suppressing the network nonaffinity, with the system deforming more affinely when hydrodynamic interactions are maximized.
引用
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页数:9
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