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J. H. Snoeijer

Publications and source records attributed to J. H. Snoeijer.

At least 19 recordsLinked to original sources

Dynamics of Poro-viscoelastic Wetting with Large Swelling

The deposition of droplets onto a swollen polymer network induces the formation of a wetting ridge at the contact line. Current models typically consider either viscoelastic effects or poroelastic effects, while polymeric gels often exhibit both properties. In this study, we investigate the growth of the wetting ridge using a comprehensive large deformation theory that integrates both dissipative mechanisms - viscoelasticity and poroelasticity. In the purely poroelastic case, following an initial instantaneous incompressible deformation, the growth dynamics exhibit scale-free behavior, independent of the elastocapillary length or system size. A boundary layer of solvent imbibition between the solid surface (in contact with the reservoir) and the region of minimal chemical potential is created. At later times, the ridge equilibrates on the diffusion timescale given by the elastocapillary length. When viscoelastic properties are incorporated, our findings show that, during the early stages (prior to the viscoelastic relaxation timescale), viscoelastic effects dominate the growth dynamics of the ridge and solvent transport is significantly suppressed. Beyond the relaxation time, the late-time dynamics closely resemble those of the purely poroelastic case. These findings are discussed in light of recent experiments, showing how our approach offers a new interpretation framework for wetting of polymer networks of increasing complexity.

cond-mat.soft↗

Soft wetting with (a)symmetric Shuttleworth effect

The wetting of soft polymer substrates brings in multiple complexities as compared to the wetting on rigid substrates. The contact angle of the liquid is no longer governed by Young's law, but is affected by the substrate's bulk and surface deformations. On top of that, elastic interfaces exhibit a surface energy that depends on how much they are stretched -- a feature known as the Shuttleworth effect (or as surface-elasticity). Here we present two models by which we explore the wetting of drops in the presence of a strong Shuttleworth effect. The first model is macroscopic in character and consistently accounts for large deformations via a neo-Hookean elasticity. The second model is based on a mesoscopic description of wetting, using a reduced description of the substrate's elasticity. While the second model is more empirical in terms of the elasticity, it enables a gradient dynamics formulation for soft wetting dynamics. We provide a detailed comparison between the equilibrium states predicted by the two models, from which we deduce robust features of soft wetting in the presence of a strong Shuttleworth effect. Specifically, we show that the (a)symmetry of the Shuttleworth effect between the "dry" and "wet" states governs horizontal deformations in the substrate. Our results are discussed in the light of recent experiments on the wettability of stretched substrates.

cond-mat.soft↗

On the singular nature of the elastocapillary ridge

The functionality of soft interfaces is crucial to many applications in biology and surface science. Recent studies have used liquid drops to probe the surface mechanics of elastomeric networks. Experiments suggest an intricate surface elasticity, also known as the Shuttleworth effect, where surface tension is not constant but depends on substrate deformation. However, interpretations have remained controversial due to singular elastic deformations, induced exactly at the point where the droplet pulls the network. Here we reveal the nature of the elastocapillary singularity on a hyperelastic substrate with various constitutive relations for the interfacial energy. First, we finely resolve the vicinity of the singularity using goal-adaptive finite element simulations. This confirms the universal validity, also at large elastic deformations, of the previously disputed Neumann's law for the contact angles. Subsequently, we derive exact solutions of nonlinear elasticity that describe the singularity analytically. These solutions are in perfect agreement with numerics, and show that the stretch at the contact line, as previously measured experimentally, consistently points to a strong Shuttleworth effect. Finally, using Noether's theorem we provide a quantitative link between wetting hysteresis and Eshelby-like forces, and thereby offer a complete framework for soft wetting in the presence of the Shuttleworth effect.

cond-mat.soft↗

Spreading on viscoelastic solids: Are contact angles selected by Neumann's law?

The spreading of liquid drops on soft substrates is extremely slow, owing to strong viscoelastic dissipation inside the solid. A detailed understanding of the spreading dynamics has remained elusive, partly owing to the difficulty in quantifying the strong viscoelastic deformations below the contact line that determine the shape of moving wetting ridges. Here we present direct experimental visualisations of the dynamic wetting ridge, complemented with measurements of the liquid contact angle. It is observed that the wetting ridge exhibits a rotation that follows exactly the dynamic liquid contact angle -- as was previously hypothesized [Karpitschka \emph{et al.} Nature Communications \textbf{6}, 7891 (2015)]. This experimentally proves that, despite the contact line motion, the wetting ridge is still governed by Neumann's law. Furthermore, our experiments suggest that moving contact lines lead to a variable surface tension of the substrate. We therefore set up a new theory that incorporates the influence of surface strain, for the first time including the so-called Shuttleworth effect into the dynamical theory for soft wetting. It includes a detailed analysis of the boundary conditions at the contact line, complemented by a dissipation analysis, which shows, again, the validity of Neumann's balance.

cond-mat.soft↗

Self-similar breakup of polymeric threads as described by the Oldroyd-B model

When a drop of fluid containing long, flexible polymers breaks up, it forms threads of almost constant thickness, whose size decreases exponentially in time. Using an Oldroyd-B fluid as a model, we show that the thread profile, rescaled by the thread thickness, converges to a similarity solution. Using the correspondence between viscoelastic fluids and non-linear elasticity, we derive similarity equations for the full three-dimensional axisymmetric flow field in the limit that the viscosity of the solvent fluid can be neglected. A conservation law balancing pressure and elastic energy permits to calculate the thread thickness exactly. The explicit form of the velocity and stress fields can be deduced from a solution of the similarity equations. Results are validated by detailed comparison with numerical simulations.

physics.flu-dyn↗

The relationship between viscoelasticity and elasticity

We consider models for elastic liquids, such as solutions of flexible polymers. They introduce a relaxation time $λ$ into the system, over which stresses relax. We study the kinematics of the problem, and clarify the relationship between Lagrangian and Eulerian descriptions, thereby showing which polymer models correspond to a nonlinear elastic deformation in the limit $λ\rightarrow\infty$. This allows us to split the change in elastic energy into reversible and dissipative parts, and thus to write an equation for the total energy, the sum of kinetic and elastic energies. As an illustration, we show how the presence or absence of an elastic limit determines the fate of an elastic thread during capillary instability, using novel numerical schemes based on our insights into the flow kinematics.

physics.flu-dyn↗

The liquid helix

From everyday experience, we all know that a solid edge can deflect a liquid flowing over it significantly, up to the point where the liquid completely sticks to the solid. Although important in pouring, printing and extrusion processes, there is no predictive model of this so-called "teapot effect". By grazing vertical cylinders with inclined capillary liquid jets, we here use the teapot effect to attach the jet to the solid and form a new structure: the liquid helix. Using mass and momentum conservation along the liquid stream, we first quantitatively predict the shape of the helix and then provide a parameter-free inertial-capillary adhesion model for the jet deflection and critical velocity for helix formation.

physics.flu-dyn↗

Turning drops into bubbles: Elastic cavitation by diffusion

Some members of the vegetal kingdom can achieve surprisingly fast movements making use of a clever combination of evaporation, elasticity and cavitation. In this process, enthalpic energy is transformed into elastic energy and suddenly released in a cavitation event which produces kinetic energy. Here we study this uncommon energy transformation by a model system: a droplet in an elastic medium shrinks slowly by diffusion and eventually transforms into a bubble by a rapid cavitation event. The experiments reveal the cavity dynamics over the extremely disparate timescales of the process, spanning 9 orders of magnitude. We model the initial shrinkage as a classical diffusive process, while the sudden bubble growth and oscillations are described using an inertial-(visco)elastic model, in excellent agreement with the experiments. Such a model system could serve as a new paradigm for motile synthetic materials.

physics.flu-dyn↗

Printing wet-on-wet: attraction and repulsion of drops on a viscous film

Wet-on-wet printing is frequently used in inkjet printing for graphical and industrial applications, where substrates can be coated with a thin liquid film prior to ink drop deposition. Two drops placed close together are expected to interact via deformations of the thin viscous film, but the nature of these capillary interactions is unknown. Here we show that the interaction can be attractive or repulsive depending on the distance separating the two drops. The distance at which the interaction changes from attraction to repulsion is found to depend on the thickness of the film, and increases over time. We reveal the origin of the non-monotonic interactions, which lies in the appearance of a visco-capillary wave on the thin film induced by the drops. Using the thin-film equation we identify the scaling law for the spreading of the waves, and demonstrate that this governs the range over which interaction is observed.

physics.flu-dyn↗

Cusp-shaped Elastic Creases and Furrows

The surfaces of growing biological tissues, swelling gels, and compressed rubbers do not remain smooth, but frequently exhibit highly localized inward folds. We reveal the morphology of this surface folding in a novel experimental setup, which permits to deform the surface of a soft gel in a controlled fashion. The interface first forms a sharp furrow, whose tip size decreases rapidly with deformation. Above a critical deformation, the furrow bifurcates to an inward folded crease of vanishing tip size. We show experimentally and numerically that both creases and furrows exhibit a universal cusp-shape, whose width scales like $y^{3/2}$ at a distance $y$ from the tip. We provide a similarity theory that captures the singular profiles before and after the self-folding bifurcation, and derive the length of the fold from large deformation elasticity.

cond-mat.soft↗

Droplets move over viscoelastic substrates by surfing a ridge

Liquid drops on soft solids generate strong deformations below the contact line, resulting from a balance of capillary and elastic forces. The movement of these drops may cause strong, potentially singular dissipation in the soft solid. Here we show that a drop on a soft substrate moves by surfing a ridge: the initially flat solid surface is deformed into a sharp ridge whose orientation angle depends on the contact line velocity. We measure this angle for water on a silicone gel and develop a theory based on the substrate rheology. We quantitatively recover the dynamic contact angle and provide a mechanism for stick-slip motion when a drop is forced strongly: the contact line depins and slides down the wetting ridge, forming a new one after a transient. We anticipate that our theory will have implications in problems such as self-organization of cell tissues or the design of capillarity-based microrheometers.

physics.flu-dyn↗

Inverted Cheerios effect: Liquid drops attract or repel by elasto-capillarity

Solid particles floating at a liquid interface exhibit a long-ranged attraction mediated by surface tension. In the absence of bulk elasticity, this is the dominant lateral interaction of mechanical origin. Here we show that an analogous long-range interaction occurs between adjacent droplets on solid substrates, which crucially relies on a combination of capillarity and bulk elasticity. We experimentally observe the interaction between droplets on soft gels and provide a theoretical framework that quantitatively predicts the migration velocity of the droplets. Remarkably, we find that while on thick substrates the interaction is purely attractive and leads to drop-drop coalescence, for relatively thin substrates a short-range repulsion occurs which prevents the two drops from coming into direct contact. This versatile, new interaction is the liquid-on-solid analogue of the "Cheerios effect". The effect will strongly influence the condensation and coarsening of drop soft polymer films, and has potential implications for colloidal assembly and in mechanobiology.

physics.flu-dyn↗

Marangoni spreading due to a localized alcohol supply on a thin water film

Bringing the interfaces of two miscible fluids into contact naturally generates strong gradients in surface tension. Here we investigate such a Marangoni-driven flow by continuously supplying isopropyl alcohol (IPA) on a film of water, using micron-sized droplets of IPA-water mixtures. These droplets create a localized depression in surface tension that leads to the opening of a circular and thin region in the water film. At the edge of the thin region, there is a rim growing and collecting the water of the film. We find that the spreading radius scales as $r \sim t^{1/2}$. This result can be explained from a balance between Marangoni and viscous stresses, assuming that the gradients in surface tension are smoothened out over the entire size of the circular opening. We derive a scaling law that accurately predicts the influence of the IPA flux as well as the thickness of the thin film at the interior of the spreading front.

physics.flu-dyn↗

How geometry determines the coalescence of low-viscosity drops

The coalescence of water drops on a substrate is studied experimentally. We focus on the rapid growth of the bridge connecting the two drops, which very quickly after contact ensues from a balance of surface tension and liquid inertia. For drops with contact angles below $90^\circ$, we find that the bridge grows with a self-similar dynamics that is characterized by a height $h\sim t^{2/3}$. By contrast, the geometry of coalescence changes dramatically for contact angles at $90^\circ$, for which we observe $h\sim t^{1/2}$, just as for freely suspended spherical drops in the inertial regime. We present a geometric model that quantitatively captures the transition from 2/3 to 1/2 exponent, and unifies the inertial coalescence of sessile drops and freely suspended drops.

physics.flu-dyn↗

Hydrodynamics of air entrainment by moving contact lines

We study the dynamics of the interface between two immiscible fluids in contact with a chemically homogeneous moving solid plate. We consider the generic case of two fluids with any viscosity ratio and of a plate moving in either directions (pulled or pushed in the bath). The problem is studied by a combination of two models, namely an extension to finite viscosity ratio of the lubrication theory and a Lattice Boltzmann method. Both methods allow to resolve, in different ways, the viscous singularity at the triple contact between the two fluids and the wall. We find a good agreement between the two models particularly for small capillary numbers. When the solid plate moves fast enough, the entrainment of one fluid into the other one can occur. The extension of the lubrication model to the case of a non-zero air viscosity, as developed here, allows us to study the dependence of the critical capillary number for air entrainment on the other parameters in the problem (contact angle and viscosity ratio).

physics.flu-dyn↗

Symmetric and Asymmetric Coalescence of Drops on a Substrate

The coalescence of viscous drops on a substrate is studied experimentally and theoretically. We consider cases where the drops can have different contact angles, leading to a very asymmetric coalescence process. Side view experiments reveal that the "bridge" connecting the drops evolves with self-similar dynamics, providing a new perspective on the coalescence of sessile drops. We show that the universal shape of the bridge is accurately described by similarity solutions of the one-dimensional lubrication equation. Our theory predicts a bridge that grows linearly in time and stresses the strong dependence on the contact angles. Without any adjustable parameters, we find quantitative agreement with all experimental observations.

physics.flu-dyn↗

Formation of surface nanobubbles and universality of their contact angles: A molecular dynamics approach

We study surface nanobubbles using molecular dynamics simulation of ternary (gas, liquid, solid) systems of Lennard-Jones fluids. They form for sufficiently low gas solubility in the liquid, i.e., for large relative gas concentration. For strong enough gas-solid attraction, the surface nanobubble is sitting on a gas layer, which forms in between the liquid and the solid. This gas layer is the reason for the universality of the contact angle, which we calculate from the microscopic parameters. Under the present equilibrium conditions the nanobubbles dissolve within less of a microsecond, consistent with the view that the experimentally found nanobubbles are stabilized by a nonequilibrium mechanism.

physics.flu-dyn↗

Thick films coating a plate withdrawn from a bath

We consider the deposition of a film of viscous liquid on a flat plate being withdrawn from a bath, experimentally and theoretically. For any plate speed $U$, there is a range of ``thick'' film solutions whose thickness scales like $U^{1/2}$ for small $U$. These solutions are realized for a partially wetting liquid, while for a perfectly wetting liquid the classical Landau-Levich-Derjaguin (LLD) film is observed, whose thickness scales like $U^{2/3}$. The thick film is distinguished from the LLD film by a dip in its spatial profile at the transition to the bath. We calculate the phase diagram for the existence of stationary film solutions as well as the film profiles, and find excellent agreement with experiment.

physics.flu-dyn↗