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Physical origin of shear-banding in jammed systems

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 Added by Guillaume Ovarlez
 Publication date 2010
  fields Physics
and research's language is English




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Jammed systems all have a yield stress. Among these materials some have been shown to shear-band but it is as yet unclear why some materials develop shear-band and some others do not. In order to rationalize existing data concerning the flow characteristics of jammed systems and in particular understand the physical origin of such a difference we propose a simple approach for describing the steady flow behaviour of yield stress fluids, which retains only basic physical ingredients. Within this frame we show that in the liquid regime the behaviour of jammed systems turns from that of a simple yield stress fluid (exhibiting homogeneous flows) to a shear-banding material when the ratio of a characteristic relaxation time of the system to a restructuring time becomes smaller than 1, thus suggesting a possible physical origin of these trends.



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139 - Guillaume Ovarlez 2010
We study the steady flow properties of different three-dimensional aqueous foams in a wide gap Couette geometry. From local velocity measurements through Magnetic Resonance Imaging techniques and from viscosity bifurcation experiments, we find that these foams do not exhibit any observable signature of shear banding. This contrasts with two previous results (Rodts et al., Europhys. Lett., 69 (2005) 636 and Da Cruz et al., Phys. Rev. E, 66 (2002) 051305); we discuss possible reasons for this dicrepancy. Moreover, the foams we studied undergo steady flow for shear rates well below the critical shear rate recently predicted (Denkov et al., Phys. Rev. Lett., 103 (2009) 118302). Local measurements of the constitutive law finally show that these foams behave as simple Herschel-Bulkley yield stress fluids.
We report experiments on hard sphere colloidal glasses that reveal a type of shear banding hitherto unobserved in soft glasses. We present a scenario that relates this to an instability arising from shear-concentration coupling, a mechanism previously thought unimportant in this class of materials. Below a characteristic shear rate $dotgamma_c$ we observe increasingly non-linear velocity profiles and strongly localized flows. We attribute this trend to very slight concentration gradients (likely to evade direct detection) arising in the unstable flow regime. A simple model accounts for both the observed increase of $dotgamma_c$ with concentration, and the fluctuations observed in the flow.
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We perform computational studies of repulsive, frictionless disks to investigate the development of stress anisotropy in mechanically stable (MS) packings. We focus on two protocols for generating MS packings: 1) isotropic compression and 2) applied simple or pure shear strain $gamma$ at fixed packing fraction $phi$. MS packings of frictionless disks occur as geometric families (i.e. parabolic segments with positive curvature) in the $phi$-$gamma$ plane. MS packings from protocol 1 populate parabolic segments with both signs of the slope, $dphi/dgamma >0$ and $dphi/dgamma <0$. In contrast, MS packings from protocol 2 populate segments with $dphi/dgamma <0$ only. For both simple and pure shear, we derive a relationship between the stress anisotropy and dilatancy $dphi/dgamma$ obeyed by MS packings along geometrical families. We show that for MS packings prepared using isotropic compression, the stress anisotropy distribution is Gaussian centered at zero with a standard deviation that decreases with increasing system size. For shear jammed MS packings, the stress anisotropy distribution is a convolution of Weibull distributions that depend on strain, which has a nonzero average and standard deviation in the large-system limit. We also develop a framework to calculate the stress anisotropy distribution for packings generated via protocol 2 in terms of the stress anisotropy distribution for packings generated via protocol 1. These results emphasize that for repulsive frictionless disks, different packing-generation protocols give rise to different MS packing probabilities, which lead to differences in macroscopic properties of MS packings.
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