Equation of State Based Slip Spring Model for Entangled Polymer Dynamics

被引:54
作者
Vogiatzis, Georgios G. [1 ]
Megariotis, Grigorios [1 ]
Theodorou, Doros N. [1 ]
机构
[1] Natl Tech Univ Athens, Sch Chem Engn, 9 Hero Polytech St,Zografou Campus, GR-15780 Athens, Greece
关键词
DISSIPATIVE PARTICLE DYNAMICS; CHAIN NETWORK SIMULATIONS; MOLECULAR-WEIGHT DEPENDENCE; STEP STRAIN PREDICTIONS; VISCOELASTIC PROPERTIES; BROWNIAN DYNAMICS; POLYPROPYLENE/POLYAMIDE INTERFACE; CONSTRAINT RELEASE; LINEAR-POLYMERS; BINARY BLENDS;
D O I
10.1021/acs.macromol.6b01705
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A mesoscopic, mixed particle-and field-based Brownian dynamics methodology for the simulation of entangled polymer melts has been developed. Polymeric beads consist of several Kuhn segments, and their motion is dictated by the Helmholtz energy of the sample, which is a sum of the entropic elasticity of chain strands between beads, slip springs, and nonbonded interactions. Following earlier works in the field [Phys. Rev. Lett. 2012, 109, 148302], the entanglement effect is introduced by the slip springs, which are springs connecting either nonsuccessive beads on the same chain or beads on different polymer chains. The terminal positions of slip springs are altered during the simulation through a kinetic Monte Carlo hopping scheme, with rate-controlled creation/destruction processes for the slip springs at chain ends. The rate constants are consistent with the free energy function employed and satisfy microscopic reversibility at equilibrium. The free energy of nonbonded interactions is derived from an appropriate equation of state, and it is computed as a functional of the local density by passing an orthogonal grid through the simulation box; accounting for it is necessary for reproducing the correct compressibility of the polymeric material. Parameters invoked by the mesoscopic model are derived from experimental volumetric and viscosity data or from atomistic molecular dynamics simulations, establishing a "bottom-up" predictive framework for conducting slip spring simulations of polymeric systems of specific chemistry. Initial configurations for the mesoscopic simulations are obtained by further coarse-graining of well-equilibrated structures represented at a greater level of detail. The mesoscopic simulation methodology is implemented for the case of cis-1,4-polyisoprene, whose structure, dynamics, thermodynamics, and linear rheology in the melt state are quantitatively predicted and validated without a posteriori fitting the results to experimental measurements.
引用
收藏
页码:3004 / 3029
页数:26
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