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Reza Azizmalayeri

Publications and source records attributed to Reza Azizmalayeri.

3 recordsLinked to original sources

Dynamic Wetting by Concentrated Granular Suspensions

Many functional materials, such as paints and inks used in applications like coating and 3D printing, are concentrated granular suspensions. In such systems, the contact line dynamics and the internal structure of the suspension interact through shear rate dependent viscosity and microstructural rearrangements. The local shear rate increases sharply near moving contact lines, leading to the non-Newtonian rheology of dense suspensions in this region. While hydrodynamic solutions can describe dilute suspensions, their applicability near advancing contact lines in dense suspensions remains unclear. This study quantifies the deviation from the Newtonian solution by systematically varying interparticle interactions through the choice of dispersion medium. We use silica particles suspended in two refractive index-matched fluids: (i) aqueous 2,2'-thiodiethanol (weak interactions) and (ii) aqueous sodium thiocyanate solution (strong interactions). These systems exhibit substantially different rheological responses, shear-thickening and yield-stress behaviour, respectively. Using astigmatism particle tracking velocimetry (APTV), we resolve the three-dimensional trajectories of tracer particles within a drop driven over a substrate, in an arrangement enabling tracking the internal flows over a long travel distance of the drop. We observe distinct flow behaviours depending on the particle interactions and the resulting suspension rheology. The more the particle interactions play a role, i.e., the more pronounced the non-Newtonian effects are, the stronger the measured flow profiles differ from the Newtonian solution to the hydrodynamic equations. In the shear-thickening suspension, a notable deviation from Newtonian behaviour is observed. Conversely, the yield-stress suspension exhibits plug flow over the substrate, with Newtonian-like behaviour restricted to the yielded region near the substrate.

cond-mat.soft

Coalescence of viscoelastic drops on a solid substrate

This study investigated the coalescence of polymer solution drops on the solid substrates. When two drops meet at their contact line on a substrate, the liquid bridge connecting the two drops increases in size with time. The height and radius of the liquid bridge have a power law dependence on time. In the early stage of drop coalescence, the exponents $\alpha$ and $\beta$ of the power law are influenced by the properties of the polymer solution. We argued that the balance between capillarity and viscoelasticity controls the process, where viscoelasticity must be considered in its full time and shear-rate dependency. As a simple proxy for the processes involved, the ratio of the polymer relaxation time to the viscous time of the drop, the elastocapillary ($Ec$), is instructive. In the vicinity of $Ec= 1$ the exponents showed a minimum and increased to lower and higher values of $Ec$. A similar dependency is observed for the damping timescales of the capillary waves. For high elastocapillary numbers, i.e. high polymer relaxation time, drop coalescence on short timescales behaved as in the low viscosity case. In addition, the bridge profile is influenced by a combination of factors including surface tension, viscosity and polymer stress. In summary, we have shown that drop coalescence is strongly influenced by the viscoelasticity of the drops.

physics.flu-dyn

Spreading of a viscoelastic drop on a solid substrate

We study the spreading of viscous and viscoelastic drops on solid substrates with different wettability. In the early stages of spreading, we find that the viscoelastic drop spreads with faster and a different power law than the Newtonian drop (i.e. aqueous glycerine solution) for the same zero shear rate viscosity. We argue that the effect of viscoelasticity is only observable for experimental time scales in the order of the internal relaxation time of the polymer solution or longer times. Near the contact line, the effective viscosity is lower for the viscoelastic drop than for the Newtonian drop. Together with its shear rate dependency, this difference in effective viscosity can explain the different spreading dynamics. We support our experimental findings with a simple perturbation model that qualitatively agrees with our findings.

cond-mat.soft