Search arXivSearch

arXiv · cond-mat/0302098

Flow phase diagrams for concentration-coupled shear banding

Abstract

After surveying the experimental evidence for concentration coupling in the shear banding of wormlike micellar surfactant solutions, we present flow phase diagrams spanned by shear stress (or strain-rate) and concentration in the two-fluid, non-local Johnson-Segalman (d-JS-phi) model. We also present macroscopic flow curves for a range of (average) concentrations. For any concentration 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. As the concentration is reduced, the width of the coexistence regime diminishes, then terminates at a non-equilibrium critical point. We outline the way in which the flow phase diagram can be reconstructed from a family of such flow curves measured for several different average concentrations. This reconstruction could be used to check new measurements of concentration differences between the coexisting bands. Our d-JS-phi model contains two spatial gradient terms describing 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, xi, for equilibrium concentration-fluctuations. We show that the phase diagrams depend on the ratio r=l/xi, 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 at the critical point.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Suzanne M Fielding, Peter D Olmsted. 2003-02-05. Flow phase diagrams for concentration-coupled shear banding. https://doi.org/10.1140/epje%2Fi2002-10128-7

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft

Taylor dispersion in a soft tube

Diffusion of a solute along a tube is enhanced by hydrodynamic flow, a phenomenon known as Taylor dispersion. In microfluidic applications, the compliance of the tube boundaries modifies the hydrodynamic flow and thus solutal transport. Here, we develop the theory of solutal dispersion in a soft, axisymmetric tube where the tube walls respond to the hydrodynamic pressure through a Winkler response. By deriving the modified macro-transport equation for the solutal concentration dynamics based on multiple-time-scale analysis, we explore the influence of softness on solutal transport for steady and pulsatile configurations. Our main finding is that softness enhances the effective advection velocity and dispersion coefficient, which might have practical implication in biology and microfluidic technology.

cond-mat.soft