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Register a new userCoupled elasticity in soft solid foams
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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.
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This paper discusses the elastic behavior of a very long crosslinked polyelectrolyte chain (Debye-Huckel chain), which is weakly charged. Therefore the response of the crosslinked chain (network) on an external constant force $f$ acting on the ends of the chain is considered. A selfconsistent variational computation of an effective field theory is employed. It is shown, that the modulus of the polyelectrolyte network has two parts: the first term represents the usual entropy elasticity of connected flexible chains and the second term takes into account the electrostatic interaction of the monomers. It is proportional to the squared crosslink density and the Debye - screening parameter.
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.
The soft-disk model previously developed and applied by Durian [D. J. Durian, Phys. Rev. Lett. 75, 4780 (1995)] is brought to bear on problems of foam rheology of longstanding and current interest, using two-dimensional systems. The questions at issue include the origin of the Herschel-Bulkley relation, normal stress effects (dilatancy), and localization in the presence of wall drag. We show that even a model that incorporates only linear viscous effects at the local level gives rise to nonlinear (power-law) dependence of the limit stress on strain rate. With wall drag, shear localization is found. Its nonexponential form and the variation of localization length with boundary velocity are well described by a continuum model in the spirit of Janiaud et al. [Phys. Rev. Lett. 97, 038302 (2006)]. Other results satisfactorily link localization to model parameters, and hence tie together continuum and local descriptions.
In the theory of weakly non-linear elasticity, Hamilton et al. [J. Acoust. Soc. Am. textbf{116} (2004) 41] identified $W = mu I_2 + (A/3)I_3 + D I_2^2$ as the fourth-order expansion of the strain-energy density for incompressible isotropic solids. Subsequently, much effort focused on theoretical and experimental developments linked to this expression in order to inform the modeling of gels and soft biological tissues. However, while many soft tissues can be treated as incompressible, they are not in general isotropic, and their anisotropy is associated with the presence of oriented collagen fiber bundles. Here the expansion of $W$ is carried up to fourth-order in the case where there exists one family of parallel fibers in the tissue. The results are then applied to acoustoelasticity, with a view to determining the second- and third-order nonlinear constants by employing small-amplitude transverse waves propagating in a deformed soft tissue.
Assemblies of purely repulsive and frictionless particles, such as emulsions or hard spheres, display very curious properties near their jamming transition, which occurs at the random close packing for mono-disperse spheres. Although such systems do not contain the long and cross-linked polymeric chains characterizing a rubber, they behave macroscopically in a similar way: the shear modulus $G$ can become infinitely smaller than the bulk modulus $B$. After reviewing recent theoretical results on the structure of such packing (in particular their coordination) I will propose an explanation for the observed scaling of the elastic moduli, and explain why the arguments both apply to soft and hard particles.
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