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Stress Overshoots in Simple Yield Stress Fluids

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 Added by Thibaut Divoux
 Publication date 2021
  fields Physics
and research's language is English




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Soft glassy materials such as mayonnaise, wet clays, or dense microgels display under external shear a solid-to-liquid transition. Such a shear-induced transition is often associated with a non-monotonic stress response, in the form of a stress maximum referred to as stress overshoot. This ubiquitous phenomenon is characterized by the coordinates of the maximum in terms of stress $sigma_text{M}$ and strain $gamma_text{M}$ that both increase as weak power laws of the applied shear rate. Here we rationalize such power-law scalings using a continuum model that predicts two different regimes in the limit of low and high applied shear rates. The corresponding exponents are directly linked to the steady-state rheology and are both associated with the nucleation and growth dynamics of a fluidized region. Our work offers a consistent framework for predicting the transient response of soft glassy materials upon start-up of shear from the local flow behavior to the global rheological observables.



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132 - G. Picard , A. Ajdari , L. Bocquet 2002
Various experiments evidence spatial heterogeneities in sheared yield stress fluids. To account for heterogeneities in the velocity gradient direction, we use a simple model corresponding to a non-monotonous local constitutive curve and study a simple shear geometry. Different types of boundary conditions are considered. Under controlled macroscopic shear stress $Sigma$, we find homogeneous flow in the bulk and a hysteretic macroscopic stress - shear rate curve. Under controlled macroscopic shear rate $dot{Gamma}$, shear banding is predicted within a range of values of $dot{Gamma}$. For small shear rates, stick slip can also be observed. These qualitative behaviours are robust when changing the boundary conditions.
317 - Guillaume Ovarlez 2012
Stability of coarse particles against gravity is an important issue in dense suspensions (fresh concrete, foodstuff, etc.). On the one hand, it is known that they are stable at rest when the interstitial paste has a high enough yield stress; on the other hand, it is not yet possible to predict if a given material will remain homogeneous during a flow. Using MRI techniques, we study the time evolution of the particle volume fraction during the flows in a Couette geometry of model density-mismatched suspensions of noncolloidal particles in yield stress fluids. We observe that shear induces sedimentation of the particles in all systems, which are stable at rest. The sedimentation velocity is observed to increase with increasing shear rate and particle diameter, and to decrease with increasing yield stress of the interstitial fluid. At low shear rate (plastic regime), we show that this phenomenon can be modelled by considering that the interstitial fluid behaves like a viscous fluid -- of viscosity equal to the apparent viscosity of the sheared fluid -- in the direction orthogonal to shear. The behavior at higher shear rates, when viscous effects start to be important, is also discussed. We finally study the dependence of the sedimentation velocity on the particle volume fraction, and show that its modelling requires estimating the local shear rate in the interstitial fluid.
Normal stresses in complex fluids lead to new flow phenomena because they can be comparable to or even larger than the shear stress itself. In addition, they are of paramount importance for formulating and testing constitutive equations for predicting non-viscometric flow behavior. Very little attention has so far been paid to the normal stresses of yield stress fluids, mainly because they are very difficult to measure. We report the first systematic study of the first and second normal stress differences, N1 (>0) and N2 (<0), in both continuous and oscillatory shear of three model yield stress fluids. We show that both normal stress differences are quadratic functions of the shear stress both above and below the shear yield stress, leading to the existence of a yield normal stress.
We develop an elasto-plastic description for the transient dynamics prior to steady flow of athermally yielding materials. Our mean-field model not only reproduces the experimentally observed non-linear time dependence of the shear-rate response to an external shear-stress, but also allows for the determination of the different physical processes involved in the onset of the re-acceleration phase after the initial critical slowing down and a distinct well defined fluidization phase. The evidenced power-law dependence of the fluidization time on the distance of the applied to an age dependent static yield stress is not universal but strongly dependent on initial conditions.
We study the rheological behavior of mixtures of foams and pastes, which can be described as suspensions of bubbles in yield stress fluids. Model systems are designed by mixing monodisperse aqueous foams and concentrated emulsions. The elastic modulus of the suspensions decreases with the bubble volume fraction. This decrease is all the sharper as the elastic capillary number (defined as the ratio of the paste elastic modulus to the bubble capillary pressure) is high, which accounts for the softening of the bubbles as compared to the paste. By contrast, the yield stress of most studied materials is not modified by the presence of bubbles. Their plastic behavior is governed by the plastic capillary number, defined as the ratio of the paste yield stress to the bubble capillary pressure. At low plastic capillary number values, bubbles behave as nondeformable inclusions, and we predict that the suspension dimensionless yield stress should remain close to unity. At large plastic capillary number values, we observe bubble breakup during mixing: bubbles are deformed by shear. Finally, at the highest bubble volume fractions, the yield stress increases abruptly: this is interpreted as a foamy yield stress fluid regime, which takes place when the paste mesoscopic constitutive elements are strongly confined in the films between the bubbles.
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