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Register a new userMicrostructural understanding of the length and stiffness dependent shear thinning in semi-dilute colloidal rods
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Complex fluids containing low concentrations of slender colloidal rods can display a high viscosity, while little flow is needed to thin the fluid. This feature makes slender rods essential constituents in industrial applications and biology. Though this behaviour strongly depends on the rod-length, so far no direct relation could be identified. We employ a library of filamentous viruses to study the effect of rod size and flexibility on the zero-shear viscosity and shear-thinning behaviour. Rheology and small angle neutron scattering data are compared to a revised version of the standard theory for ideally stiff rods, which incorporates a complete shear-induced dilation of the confinement. While the earlier predicted length-independent pre-factor of the restricted rotational diffusion coefficient is confirmed by varying the length and concentration of the rods, the revised theory correctly predicts the shear thinning behaviour as well as the underlying orientational order. These results can be directly applied to understand the manifold systems based on rod-like colloids and design new materials.
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We assess the possibility of shear banding of semidilute rod-like colloidal suspensions under steady shear ow very close to the isotropic-nematic spinodal, using a combination of rheology, small angle neutron scattering, and laser Doppler velocimetry. Model systems are employed which allow for a length and stiffness variation of the particles. The rheological signature reveals that these systems are strongly shear thinning at moderate shear rates. It is shown that the longest and most flexible rods undergo the strongest shear thinning and have the greatest potential to form shear bands. Although we find a small but significant gradient of the orientational order parameter throughout the gap of the shear cell, no shear banding transition is tractable in the region of intermediate shear rates. At very low shear rates, gradient banding and wall slip occur simultaneously, but the shear bands are not stable over time.
In a microrheological set-up a single probe particle immersed in a complex fluid is exposed to a strong external force driving the system out of equilibrium. Here, we elaborate analytically the time-dependent response of a probe particle in a dilute suspension of Brownian particles to a large step-force, exact in first order of the density of the bath particles. The time-dependent drift velocity approaches its stationary state value exponentially fast for arbitrarily small driving in striking contrast to the power-law prediction of linear response encoded in the long-time tails of the velocity autocorrelation function. We show that the stationary-state behavior depends nonanalytically on the driving force and connect this behavior to the persistent correlations in the equilibrium state. We argue that this relation holds generically. Furthermore, we elaborate that the fluctuations in the direction of the force display transient superdiffusive behavior.
We use molecular dynamics computer simulations to investigate the relaxation dynamics of a simple model for a colloidal gel at a low volume fraction. We find that due to the presence of the open spanning network this dynamics shows at low temperature a non-trivial dependence on the wave-vector which is very different from the one observed in dense glass-forming liquids. At high wave vectors the relaxation is due to the fast cooperative motion of the branches of the gel network, whereas at low wave vectors the overall rearrangements of the heterogeneous structure produce the relaxation process.
We present simulations for the steady-shear rheology of a model adhesive dispersion. We vary the range of the attractive forces $u$ as well as the strength of the dissipation $b$. For large dissipative forces, the rheology is governed by the Weisenberg number $ text{Wi}sim bdotgamma/u$ and displays Herschel-Bulkley form $sigma = sigma_y+ctext{Wi}^ u$ with exponent $ u=0.45$. Decreasing the strength of dissipation, the scaling with $text{Wi}$ breaks down and inertial effects show up. The stress decreases via the Johnson-Samwer law $Deltasigmasim T_s^{2/3}$, where temperature $T_s$ is exclusively due to shear-induced vibrations. During flow particles prefer to rotate around each other such that the dominant velocities are directed tangentially to the particle surfaces. This tangential channel of energy dissipation and its suppression leads to a discontinuity in the flow curve, and an associated discontinuous shear thinning transition. We set up an analogy with frictional systems, where the phenomenon of discontinuous shear thickening occurs. In both cases tangential forces, frictional or viscous, mediate a transition from one branch of the flowcurve with low tangential dissipation to one with large tangential dissipation.
Catalytic colloidal swimmers that propel due to self-generated fluid flows exhibit strong affinity for surfaces. We here report experimental measurements of significantly different velocities of such microswimmers in the vicinity of substrates made from different materials. We find that velocities scale with the solution contact angle $theta$ on the substrate, which in turn relates to the associated hydrodynamic substrate slip length, as $Vpropto(costheta+1)^{-3/2}$. We show that such dependence can be attributed to osmotic coupling between swimmers and substrate. Our work points out that hydrodynamic slip at the wall, though often unconsidered, can significantly impact the self-propulsion of catalytic swimmers.
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