Age-dependent transient shear banding in soft glasses

We study numerically the formation of long-lived transient shear bands during shear startup within two models of soft glasses (a simple fluidity model and an adapted "soft glassy rheology" model). The degree and duration of banding depends strongly on the applied shear rate, and on sample age before shearing. In both models the ultimate steady flow state is homogeneous at all shear rates, consistent with the underlying constitutive curve being monotonic. However, particularly in the soft glassy rheology case, the transient bands can be extremely long lived. The banding instability is neither "purely viscous" nor "purely elastic" in origin, but is closely associated with stress overshoot in startup flow.     

Why does shear banding behave like first-order phase transitions? Derivation of a potential from a mechanical constitutive model

Numerous numerical and experimental evidence suggest that shear banding behavior looks like first-order phase transitions. In this paper, we demonstrate that this correspondence is actually established in the so-called non-local diffusive Johnson-Segalman model (the DJS model), a typical mechanical constitutive model that has been widely used for describing shear banding phenomena. In the neighborhood of the critical point, we apply the reduction procedure based on the center manifold theory to the governing equations of the DJS model. As a result, we obtain a time evolution equation of the flow field that is equivalent to the time-dependent Ginzburg-Landau (TDGL) equations for modeling thermodynamic first-order phase transitions. This result, for the first time, provides a mathematical proof that there is an analogy between the mechanical instability and thermodynamic phase transition at least in the vicinity of the critical point of the shear banding of DJS model. Within this framework, we can clearly distinguish the metastable branch in the stress-strain rate curve around the shear banding region from the globally stable branch. A simple extension of this analysis to a class of more general constitutive models is also discussed. Numerical simulations for the original DJS model and the reduced TDGL equation is performed to confirm the range of validity of our reduction theory.     

Ideal shear banding in metallic glass

As the most fundamental deformation mechanism in metallic glasses (MGs), the shear banding has attracted a lot of attention and interest over the years. However, the intrinsic properties of the shear band are affected and even substantially changed by the influence of non-rigid testing machine that cannot be completely removed in real compression tests. In particular, the duration of the shear banding event is prolonged due to the recovery of the stressed compliant frame of testing machine and therefore the temperature rise at the operating shear band is, more or less, underestimated in previous literatures. In this study, we propose a model for the ‘ideal’ shear banding in metallic glass. The compliance of the testing machine is eliminated, and the intrinsic shear banding process is extracted and investigated. Two important physical parameters, the sliding speed and the temperature of shear band, are calculated and analysed on the basis of the thermo-mechanical coupling. Strain-rate hardening is proposed to compensate thermal softening and stabilise the shear band. The maximum value of the sliding speed is found to be on the order of 10 m/s at least, and the critical temperature at which strain-rate hardening begins to take effect should reach as high as 0.9T_g (T_g is the glass transition temperature) for a stable shear banding event in metallic glass according to the early experimental data. This model can help to understand and control the shear banding and therefore the deformation in MGs.     

Flow phase diagrams for concentration-coupled shear banding

After surveying the experimental evidence for concentration coupling in the shear banding of wormlike micellar surfactant systems, we present flow phase diagrams spanned by shear stress Σ (or strain rate ) and concentration, calculated within the two-fluid, non-local Johnson-Segalman (d-JS-φ) model. We also give results for the macroscopic flow curves Σ(ˉ,ˉφ) for a range of (average) concentrations ˉφ. For any concentration that is high enough to give shear banding, the flow curve shows the usual non-analytic kink at the onset of banding, followed by a coexistence “plateau” that slopes upwards, dΣ/dˉ > 0. As the concentration is reduced, the width of the coexistence regime diminishes and eventually terminates at a non-equilibrium critical point [Σ_c,ˉφ_c,ˉ_c]. We outline the way in which the flow phase diagram can be reconstructed from a family of such flow curves, Σ(ˉ,ˉφ), measured for several different values of ˉφ. This reconstruction could be used to check new measurements of concentration differences between the coexisting bands. Our d-JS-φ model contains two different spatial gradient terms that describe the interface between the shear bands. The first is in the viscoelastic constitutive equation, with a characteristic (mesh) length l. The second is in the (generalised) Cahn-Hilliard equation, with the characteristic length ξ for equilibrium concentration-fluctuations. We show that the phase diagrams (and so also the flow curves) depend on the ratio r ≡ l /ξ, with loss of unique state selection at r = 0. We also give results for the full shear-banded profiles, and study the divergence of the interfacial width (relative to l and ξ) at the critical point. Received: 20 December 2002 / Accepted: 24 April 2003 / Published online: 11 June 2003 RID="a" ID="a"e-mail: physf@irc.leeds.ac.uk RID="b" ID="b"e-mail: p.d.olmsted@leeds.ac.uk     

Shear banding in molecular dynamics of polymer melts

In order to establish constitutive equations for a viscoelastic fluid uniform shear flow is usually required. However, in the last 10 years S. Q. Wang and co-workers have demonstrated that some entangled polymers do not flow with the uniform shear rate as usually assumed, but instead choose to separate into fast and slow flowing regions. This phenomenon, known as shear banding, causes flow instabilities and in principle invalidates all rheological measurements when it occurs. In this Letter we report the first observation of shear banding in molecular dynamics simulations of entangled polymer melts. We show that our observations are in a very good agreement with the phenomenology developed by Fielding and Olmsted. Our findings provide a simple way of validating the empirical macroscopic phenomenology of shear banding.     

Flow birefringence,stress optical rule and rheology of four micellar solutions with the same low shear viscosity

The flow birefringence and the rheological properties of four viscoelastic solutions having nearly the same zero shear viscosity and subjected to shear flows are investigated in the linear and non-linear domains. The surfactant used for the samples is the cetyltrimethylammonium chloride in water at the concentration of 100 mmol/l with an organic salt, the sodium salicylate. The low shear viscosity curve versus the salt concentration is non-monotonic and has two maxima separated by a minimum forming four domains in which the salt concentration is chosen. For the two solutions belonging to the inner branch, i.e. between the two maxima, a simple Maxwellian behaviour is observed and shear banding occurs as confirmed by the flow birefringence pictures. Contrary to the results of P. Fisher (1996) where the unstable flow regime is restricted to the first decreasing part of the low shear viscosity curve of a cetylpyridinium chloride solution, we show that shear banding exits in a wider domain of the salt concentration. Received 18 November 2002 / Published online: 1 April 2003 RID="a" ID="a"e-mail: Decruppe@lpli.sciences.univ-metz.fr     

Shear banding and flow-concentration coupling in colloidal glasses

We report experiments on hard-sphere colloidal glasses that show a type of shear banding hitherto unobserved in soft glasses. We present a scenario that relates this to an instability due to shear-concentration coupling, a mechanism previously thought unimportant in these materials. Below a characteristic shear rate γ(c) we observe increasingly nonlinear and localized velocity profiles. We attribute this to very slight concentration gradients in the unstable flow regime. A simple model accounts for both the observed increase of γ(c) with concentration, and the fluctuations in the flow.     

Linear instability of planar shear banded flow

We study the linear stability of planar shear banded flow with respect to perturbations with wave vector in the plane of the banding interface, within the nonlocal Johnson-Segalman model. We find that perturbations grow in time, over a range of wave vectors, rendering the interface linearly unstable. Results for the unstable eigenfunction are used to discuss the nature of the instability. We also comment on the stability of phase separated domains to shear flow in model H.     

Two-dimensional perturbations in a scalar model for shear banding

We present an analytical study of a toy model for shear banding, without normal stresses, which uses a piecewise linear approximation to the flow curve (shear stress as a function of shear rate). This model exhibits multiple stationary states, one of which is linearly stable against general two-dimensional perturbations. This is in contrast to analogous results for the Johnson-Segalman model, which includes normal stresses, and which has been reported to be linearly unstable for general two-dimensional perturbations. This strongly suggests that the linear instabilities found in the Johnson-Segalman can be attributed to normal stress effects.     

Elusiveness of fluid-fluid demixing in additive hard-core mixtures

The conjecture that when an additive hard-core mixture phase separates when one of the phases is spatially ordered, well supported by considerable evidence, is in contradiction with some simulations of a binary mixture of hard cubes on cubic lattices. By extending Rosenfeld's fundamental measure theory to lattice models we show that the phase behavior of this mixture is far more complex than simulations show, exhibiting regions of stability of several smectic, columnar, and solid phases, but no fluid-fluid demixing. A comparison with the simulations show that they are, in fact, compatible with a fluid-columnar demixing transition, thus bringing this model into the same demixing scheme as the rest of additive hard-core mixtures.     

Kinetics of shear banding in a bulk metallic glass monitored by acoustic emission measurements

Detailed acoustic emission (AE) and surface microscopy investigations of the kinetics of shear banding in bulk Zr_52.5Ti₅Cu_17.9Ni_14.6Al₁₀ metallic glass at room temperature are presented. The shear band propagates in a jump-like mode as reflected by numerous AE bursts. The time distribution and cluster statistical analysis of AE time series revealed, firstly, that there are two shear banding processes notably different in their spatial scales and, secondly, that formation of shear bands at large strains can be correlated in time and space. Independence of the AE characteristics on the current stress magnitude implies that shear band propagation could not be interpreted as a shear front motion in a viscous Newtonian-like medium. The AE response to shear banding is to a certain extent similar to that of a moving dislocation pile-up escaping to a free surface. It is emphasized that AE and microscopic features of shear banding in the bulk metallic glass are very nearly the same as those found earlier for melt-spun ribbon glasses, indicating that the change in the quenching rate by about four orders of magnitude does not cause the kinetics of shear band nucleation and propagation to vary considerably.     

Nonlinear dynamics of an interface between shear bands

We study numerically the nonlinear dynamics of a shear banding interface in two-dimensional planar shear flow, within the nonlocal Johnson-Segalman model. Consistent with a recent linear stability analysis, we find that an initially flat interface is unstable with respect to small undulations for a sufficiently small ratio of the interfacial width l to cell length L(x). The instability saturates in finite amplitude interfacial fluctuations. For decreasing l/L(x) these undergo a nonequilibrium transition from simple traveling interfacial waves with constant average wall stress, to periodically rippling waves with a periodic stress response. When multiple shear bands are present we find erratic interfacial dynamics and a stress response suggesting low dimensional chaos.     

Simulations of complex fluids by mixed lattice Boltzmann—finite difference methods

We present the numerical results of simulations of complex fluids under shear flow. We employ a mixed approach which combines the lattice Boltzmann method for solving the Navier–Stokes equation and a finite difference scheme for the convection–diffusion equation. The evolution in time of shear banding phenomenon is studied. This is allowed by the presented numerical model which takes into account the evolution of local structures and their effect on fluid flow.     

Spatiotemporal oscillations and rheochaos in a simple model of shear banding

We study a simple model of shear banding in which the flow-induced phase is destabilized by coupling between flow and microstructure (wormlike micellar length). By varying the strength of instability and the applied shear rate, we find a rich variety of oscillatory and chaotic shear banded flows. At low shear and weak instability, the induced phase pulsates next to one wall of the flow cell. For stronger instability, high shear pulses ricochet across the cell. At high shear we see oscillating bands on either side of central defects. We discuss our results in the context of recent experiments.     

Slip, yield, and bands in colloidal crystals under oscillatory shear

We study dense colloidal crystals under oscillatory shear using a confocal microscope. At large strains the crystals yield and the suspensions form shear bands. The pure harmonic response exhibited by the suspension rules out the applicability of nonlinear rheology models typically used to describe shear banding in other types of complex fluids. Instead, we show that a model based on the coexistence of linearly responding phases of the colloidal suspension accounts for the observed flows. These results highlight a new use of oscillatory measurements in distinguishing the contribution of linear and nonlinear local rheology to a globally nonlinear material response.     

Comparison of shear banding in BMGs due to thermal-softening and free volume creation

This paper reports a comparative study of shear banding in BMGs resulting from thermal softening and free volume creation. Firstly, the effects of thermal softening and free volume creation on shear instability are discussed. It is known that thermal softening governs thermal shear banding, hence it is essentially energy related. However, compound free volume creation is the key factor to the other instability, though void-induced softening seems to be the counterpart of thermal softening. So, the driving force for shear instability owing to free volume creation is very different from the thermally assisted one. In particular, long wave perturbations are always unstable owing to compound free volume creation. Therefore, the shear instability resulting from coupled compound free volume creation and thermal softening may start more like that due to free volume creation. Also, the compound free volume creation implies a specific and intrinsic characteristic growth time of shear instability. Finally, the mature shear band width is governed by the corresponding diffusions (thermal or void diffusion) within the band. As a rough guide, the dimensionless numbers: Thermal softening related number B, Deborah number (denoting the relation of instability growth rate owing to compound free volume and loading time) and Lewis number (denoting the competition of different diffusions) show us their relative importance of thermal softening and free volume creation in shear banding. All these results are of particular significance in understanding the mechanism of shear banding in bulk metallic glasses (BMGs). Supported by the Chinese Academy of Sciences under the project “Multi-Scale Complex System” (Grant No. KJCX-SW-L08), the National Natural Science Foundation of China (Grant Nos. 10725211 and 10721202), and the Doctorial Start-up Fund of Hunan University of Science and Technology (Grant No. E50840)     

Demixing of a binary mixture in slit-like pores at high temperatures

We investigate the fluid—fluid demixing transitions in the case of adsorption of so-called symmetric binary mixtures in slit-like pores at temperatures higher than the bulk gas—liquid critical temperature. The aim of the study is to determine how the demixing of such mixtures in the pores depends on the bulk phase composition and on the parameters characterizing the pore. The calculations have been carried out by means of a density functional theory. In the case of an equimolar bulk mixture, the demixing transition inside the pore occurs only when the adsorption potentials of both species are identical. The occurrence of this transition is manifested by a cusp in the adsorption isotherm. For nonequimolar bulk phase compositions, the transition can also take place if the adsorption energies of both components are different. However, the difference in the adsorption energies should be small enough, otherwise a continuous demixing takes place. For non-equimolar compositions two branches of the grand canonical potential intersect, whereas for equimolar bulk composition they meet tangentially. We have determined phase behaviour for several model systems.     

Spatiotemporal rheochaos in nematic hydrodynamics

Motivated by recent observations of rheochaos in sheared wormlike micelles, we study the coupled nonlinear partial differential equations for the hydrodynamic velocity and order-parameter fields in a sheared nematogenic fluid. In a suitable parameter range, we find irregular, dynamic shear banding and establish by decisive numerical tests that the chaos we observe in the model is spatiotemporal in nature.     

A minimal model for vorticity and gradient banding in complex fluids

A general phenomenological reaction-diffusion model for flow-induced phase transitions in complex fluids is presented. The model consists of an equation of motion for a nonconserved composition variable, coupled to a Newtonian stress relation for the reactant and product species. Multivalued reaction terms allow for different homogeneous phases to coexist with each other, resulting in banded composition and shear rate profiles. The one-dimensional equation of motion is evolved from a random initial state to its final steady state. We find that the system chooses banded states over homogeneous states, depending on the shape of the stress constitutive curve and the magnitude of the diffusion coefficient. Banding in the flow gradient direction under shear rate control is observed for shear-thinning transitions, while banding in the vorticity direction under stress control is observed for shear-thickening transitions. Received 1 April 2001 and Received in final form 16 June 2001     

Nonaxisymmetric instability of shear-banded Taylor-Couette flow

Recent experiments show that shear-banded flows of semidilute wormlike micelles in Taylor-Couette geometry exhibit a flow instability in the form of Taylor-like vortices. Here we perform the nonaxisymmetric linear stability analysis of the diffusive Johnson-Segalman model of shear banding and show that the nature of this instability depends on the applied shear rate. For the experimentally relevant parameters, we find that at the beginning of the stress plateau the instability is driven by the interface between the bands, while most of the stress plateau is occupied by the bulk instability of the high-shear-rate band. Our work significantly alters the recently proposed stability diagram of shear-banded flows based on axisymmetric analysis.