Universal phase-field mixture representation of thermodynamics and shock-wave mechanics in porous soft biologic continua.

Phys Rev E

Terminal Effects Division, DEVCOM ARL, Aberdeen Proving Ground, Maryland 21005-5066, USA.

Published: September 2024

A continuum mixture theory is formulated for large deformations, thermal effects, phase interactions, and degradation of soft biologic tissues suitable at high pressures and low to very high strain rates. Tissues consist of one or more solid and fluid phases and can demonstrate nonlinear anisotropic elastic, viscoelastic, thermoelastic, and poroelastic physics. Under extreme deformations or shock loading, tissues may fracture, tear, or rupture. Existing models do not account for all physics simultaneously, and most poromechanics and soft-tissue models assume incompressibility of some or all constituents, generally inappropriate for modeling shock waves or extreme compressions. Motivated by these prior limitations, a thermodynamically consistent formulation that combines a continuum theory of mixtures, compressible nonlinear anisotropic thermoelasticity, viscoelasticity, and phase-field mechanics of fracture is constructed to resolve the pertinent physics. A metric tensor of generalized Finsler space supplies geometric insight on effects of rearrangements of microstructure, for example degradation, growth, and remodeling. Shocks are modeled as singular surfaces. Hugoniot states and shock decay are analyzed: Solutions account for concurrent viscoelasticity, fracture, and interphase momentum and energy exchange not all contained in previous analyses. Suitability of the framework for representing blood, skeletal muscle, and liver is demonstrated by agreement with experimental data and observations across a range of loading rates and pressures. Insight into previously unresolved physics is obtained, for example importance of rate sensitivity of damage and quantification of effects of dissipation from viscoelasticity and phase interactions on shock decay.

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http://dx.doi.org/10.1103/PhysRevE.110.035001DOI Listing

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