A statistically-based continuum theory for polymers with transient networks. (October 2017)

• Record Type: Journal Article
• Authors: Vernerey, Franck J.; Long, Rong; Brighenti, Roberto
• Is Part Of: Journal of the mechanics and physics of solids. Volume 107(2017:Oct.)
• Page Start: 1
• Page End: 20
• Publication Date: 2017-10
• Subjects: Polymer mechanics -- Visco-elasticity -- Transient response -- Dynamic cross-links -- Statistical theory; Mechanics, Applied -- Periodicals; Solids -- Periodicals; Mechanics -- Periodicals; Mécanique appliquée -- Périodiques; Solides -- Périodiques; Mechanics, Applied; Solids; Periodicals; 531.05
• DOI: 10.1016/j.jmps.2017.05.016
• Languages: English
• ISSNs: 0022-5096

Abstract

Highlights: A statistically-based continuum theory is proposed to model the transient response of polymers. An evolution equation is derived for a distribution tensor that characterizes the polymer network. This tensor enables a direct connection between chain statistics and visco-elastic response. The theory can incorporate various elastic and dissipative mechanisms from the molecular scale. Abstract: We present a physics-based theoretical framework to describe the transient mechanical response of polymers undergoing finite deformation. For this, a statistical description of the polymer network is provided by a distribution function that is allowed to evolve in time due to a combination of deformation and chain reconfiguration enabled by transient cross-links. After presenting the evolution law for the chain distribution function, we show that, using classical thermodynamics, one can determine how the entropy, elastic energy and true stress evolve in terms of the network configuration. In particular, we introduce the concept of distribution tensor, which enables a clean transition between the network statistics, its continuum representation and the macroscopic polymer response. In the context of Gaussian statistics, it is further shown that this tensor follows its own evolution law, enabling a simple handling of visco-elastic rubbers. The model degenerates to classical rubber elasticity when cross-links are permanent, while the case of viscous fluids is recovered for fast cross-link kinetics. The generality of the framework as well as its relevance to modeling a number of important dissipative processes occurring in polymers using a continuum approach are also discussed.