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Register a new userMicroscopic interactions and emerging elasticity in model soft particulate gels
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We discuss a class of models for particulate gels in which the particle contacts are described by an effective interaction combining a two-body attraction and a three-body angular repulsion. Using molecular dynamics, we show how varying the model parameters allows us to sample, for a given gelation protocol, a variety of gel morphologies. For a specific set of the model parameters, we identify the local elastic structures that get interlocked in the gel network. Using the analytical expression of their elastic energy from the microscopic interactions, we can estimate their contribution to the emergent elasticity of the gel and gain new insight into its origin.
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We present a Landau type theory for the non-linear elasticity of biopolymer gels with a part of the order parameter describing induced nematic order of fibers in the gel. We attribute the non-linear elastic behavior of these materials to fiber alignment induced by strain. We suggest an application to contact guidance of cell motility in tissue. We compare our theory to simulation of a disordered lattice model for biopolymers. We treat homogeneous deformations such as simple shear, hydrostatic expansion, and simple extension, and obtain good agreement between theory and simulation. We also consider a localized perturbation which is a simple model for a contracting cell in a medium.
A simple and popular constitutive model used to describe the compressional strength of a consolidating strongly cohesive particulate gel is tested further with new experimental data. Strong cohesive particulate gels have variously been described as being ratchet (poro) elastic, on the one hand, and as having a yield stress in compression, on the other, to the point where same groups of workers have used both descriptions at one time or another. The dichotomy is real though as such gels do show a hitherto somewhat puzzling elastic-plastic duality. This can be explained in part by the strong concentration dependence of the modulus since this leads to irreversible volumetric strain-hardening, in effect, the ratchet; but only in small part. The real problem seems to be that, until very recently, most work on consolidation has neglected what what Michaels and Bolger told us to do over 50 years ago, viz. to take into wall adhesion into account, most cohesive particulate gels being adhesive too. Since wall adhesive failure is plastic in character, the simplest non-linear elastic model of compressive strength can be combined with the simplest possible model of wall debonding to produce a approximate complete constitutive description. Examples of the use of such a description in detailed modelling of consolidation equilibrium can be found in refs 10-12. Consolidation dynamics with wall adhesion is a substantial modelling challenge remaining to be tackled.
Rheological measurements of model colloidal gels reveal that large variations in the shear moduli as colloidal volume-fraction changes are not reflected by simple structural parameters such as the coordination number, which remains almost a constant. We resolve this apparent contradiction by conducting a normal mode analysis of experimentally measured bond networks of the gels. We find that structural heterogeneity of the gels, which leads to floppy modes and a nonaffine-affine crossover as frequency increases, evolves as a function of the volume fraction and is key to understand the frequency dependent elasticity. Without any free parameters, we achieve good qualitative agreement with the measured mechanical response. Furthermore, we achieve universal collapse of the shear moduli through a phenomenological spring-dashpot model that accounts for the interplay between fluid viscosity, particle dissipation, and contributions from the affine and non-affine network deformation.
Elasticity of soft materials can be greatly influenced by the presence of air bubbles. Such a capillary effect is expected for a wide range of materials, from polymer gels to concentrated emulsions and colloidal suspensions. Whereas experimental results and theory exist for describing the elasto-capillary behavior of bubbly materials (i.e. with moderate gas volume fractions), foamy systems still require a dedicated study in order to increase our understanding of elasticity in aerated materials over the full range of gas volume fractions. Here we elaborate well-controlled foams with concentrated emulsion and we measure their shear elastic modulus as a function of gas fraction, bubble size and elastic modulus of the emulsion. Such complex foams possess the elastic features of both the bubble assembly and the interstitial matrix. Moreover, their elastic modulus is shown to be governed by two parameters, namely the gas volume fraction and the elasto-capillary number, defined as the ratio of the emulsion modulus with the bubble capillary pressure. We connect our results for foams with existing data for bubbly systems and we provide a general view for the effect of gas bubbles in soft elastic media. Finally, we suggest that our results could be useful for estimating the shear modulus of aqueous foams and emulsions with multimodal size distributions.
We report detailed theoretical investigations of the micro-mechanics and bulk elastic properties of composites consisting of randomly distributed stiff fibers embedded in an elastic matrix in two and three dimensions. Recent experiments published in Physical Review Letters [102, 188303 (2009)] have suggested that the inclusion of stiff microtubules in a softer, nearly incompressible biopolymer matrix can lead to emergent compressibility. This can be understood in terms of the enhancement of the compressibility of the composite relative to its shear compliance as a result of the addition of stiff rod-like inclusions. We show that the Poissons ratio $ u$ of such a composite evolves with increasing rod density towards a particular value, or {em fixed point}, independent of the material properties of the matrix, so long as it has a finite initial compressibility. This fixed point is $ u=1/4$ in three dimensions and $ u=1/3$ in two dimensions. Our results suggest an important role for stiff filaments such as microtubules and stress fibers in cell mechanics. At the same time, our work has a wider elasticity context, with potential applications to composite elastic media with a wide separation of scales in stiffness of its constituents such as carbon nanotube-polymer composites, which have been shown to have highly tunable mechanics.
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