arXiv subjects

Jacco H. Snoeijer

Publications and source records attributed to Jacco H. Snoeijer.

At least 19 recordsLinked to original sources

arXiv2026

Butter on a hot pan: self-regulating dynamics of melt-lubricated sliding

When solids melt while sliding down heated inclines, their motion is governed by a complex coupling between heat transfer, phase change, gravity and viscous dissipation. Despite relevance across a variety of domains, like kitchen physics, geophysics, tribology, and manufacturing, this coupled problem lacks understanding and quantitative experimental validation. Here we report experiments with ice and paraffin wax on a temperature-controlled ramp that achieve terminal velocities from 0.01 m/s to 2 m/s across wide parameter ranges. We develop a theoretical model that captures the self-regulating feedback between melt-layer thickness, sliding velocity, and heat transfer. Without any adjustable parameters, our model collapses all measurements, validating the fundamental mechanism and enabling predictions for analogous systems.

physics.flu-dyn↗

arXiv2026

Viscoelasticity Enhances Contactless Adhesion of Soft Substrates

Understanding adhesion is essential for describing stability, friction, and interfacial dynamics. Here, we investigate the adhesion force dynamics between a rigid sphere and a soft surface without direct contact, mediated by a viscous fluid. By combining controlled experiments, a first-principles visco-elastohydrodynamic theory, and numerical simulations, we demonstrate that viscoelastic relaxation fundamentally modifies elastohydrodynamic adhesion. Rather than simply dissipating energy, viscoelasticity causes the substrate to behave transiently as a stiffer solid, enhancing the maximum adhesive force, changing the early-time force growth for $t^{2/3}$ to $t^{1/3}$, shortening the interaction time, and giving rise to new scaling laws governed by the Deborah number. The two proposed dimensionless parameters, the softness parameter and the Deborah number, define a unified phase diagram connecting three distinct adhesion regimes: classical Reynolds lubrication, elastohydrodynamic adhesion, and the newly identified visco-elastohydrodynamic regime.

cond-mat.soft↗

arXiv2026

How elasticity affects bubble pinch-off

The pinch-off of bubbles in viscoelastic liquids is a fundamental process that has received little attention compared to viscoelastic drop pinch-off. While these processes exhibit qualitative similarities, the dynamics of the pinch-off process are significantly different. When a drop of a dilute polymer solution pinches off, a thread is known to develop that prevents breakup due the diverging polymer stresses. Conversely, our experiments reveal that this thread is absent for bubble pinch-off in dilute polymer solutions. We show that a thread becomes apparent only for high polymer concentrations, where the pinch-off dynamics become very sensitive to the size of the needle from which the bubble detaches. The experiments are complemented by numerical simulations and analytical modeling using the Oldroyd-B model, which capture the dilute regime. The model shows that polymer stresses are still singular during bubble pinch-off, but the divergence is much weaker as compared to drop pinch-off. This explains why, in contrast to droplets, viscoelastic bubble-threads do not appear for dilute suspensions but require large polymer concentrations

cond-mat.soft↗

arXiv2025

Collective Effects in Breath Figures

Breath figures are the complex patterns that form when water vapor condenses into liquid droplets on a surface. The primary question concerning breath figures is how the condensing vapor is allocated between the growth of existing droplets and the nucleation of new ones. Although numerous theoretical studies have concentrated on scenarios resulting in highly polydisperse droplet ensembles, a companion paper [Bouillant {\em et al.}, submitted] demonstrates that nearly monodisperse patterns can be achieved on defect-free substrates in a diffusion-controlled regime. The objective of this work is to present a theoretical framework that elucidates the formation and evolution of nearly-monodisperse patterns in breath figures. We discover that, following a short nucleation phase, the number of droplets remains constant over an extensive range of timescales due to collective effects mediated by the diffusion of vapor. The spatial extent of these diffusive interactions is identified through asymptotic matching, based on which we provide an accurate description of breath figures through a mean-field model. The model accounts for the sub-diffusive growth of droplets as well as for the arrest of nucleating new droplets, and reveal the scaling laws for the droplet density observed in experiments. Finally, droplets expand and ultimately coalesce, which is shown to trigger a scale-free coarsening of the breath figures.

physics.flu-dyn↗

arXiv2024

Interfacial dripping faucet: generating monodisperse liquid lenses

We present a surface analog to a dripping faucet, where a viscous liquid slides down an immiscible meniscus. Periodic pinch-off of the dripping filament is observed, generating a succession of monodisperse floating lenses. We show that this interfacial dripping faucet can be described analogously to its single-phase counterpart, replacing surface tension by the spreading coefficient, and even undergoes a transition to a jetting regime. This liquid/liquid/gas system opens perspectives for the study of the dynamics of emulsions at interfaces.

physics.flu-dyn↗

arXiv2024

Viscoelastic lubrication of a submerged cylinder sliding down an incline

Lubrication flows between two solid surfaces can be found in a variety of biological and engineering settings. In many of these systems, the lubricant exhibits viscoelastic properties, which modify the associated lubrication forces. Here, we experimentally study viscoelastic lubrication by considering the motion of a submerged cylinder sliding down an incline. We demonstrate that cylinders move faster when released in a viscoelastic Boger liquid compared to a Newtonian liquid with similar viscosity. Cylinders exhibit pure sliding motion in viscoelastic liquids, in contrast to the stick-slip motion observed in Newtonian liquids. We rationalize our results by using the second-order fluid model, which predicts a lift force on the cylinder arising from the normal-stress differences provided by the dissolved polymers. The interplay between viscoelastic lift, viscous friction, and gravity leads to a prediction for the sliding speed, which is consistent with our experimental results for weakly viscoelastic flows. Finally, we identify a remarkable difference between the lubrication of cylindrical and spherical contacts, as the latter does not exhibit any lift for weak viscoelasticity.

cond-mat.soft↗

arXiv2024

Viscoelastic wetting transition: beyond lubrication theory

The dip-coating geometry, where a solid plate is withdrawn from or plunged into a liquid pool, offers a prototypical example of wetting flows involving contact-line motion. Such flows are commonly studied using the lubrication approximation approach which is intrinsically limited to small interface slopes and thus small contact angles. Flows for arbitrary contact angles, however, can be studied using a generalized lubrication theory that builds upon viscous corner flow solutions. Here we derive this generalized lubrication theory for viscoelastic liquids that exhibit normal stress effects and are modelled using the second-order fluid model. We apply our theory to advancing and receding contact lines in the dip-coating geometry, highlighting the influence of viscoelastic normal stresses for contact line motion at arbitrary contact angle.

cond-mat.soft↗

arXiv2024

Sticking without contact: Elastohydrodynamic adhesion

The adhesion between dry solid surfaces is typically governed by contact forces, involving surface forces and elasticity. For surfaces immersed in a fluid, out-of-contact adhesion arises due to the viscous resistance to the opening of the liquid gap. While the adhesion between dry solids is described by the classical JKR theory, there is no equivalent framework for the wet adhesion of soft solids. Here, we investigate theoretically the viscous adhesion emerging during the separation of a sphere from an elastic substrate. The suction pressure within the thin viscous film between the solids induces significant elastic displacements. Unexpectedly, the elastic substrate closely follows the motion of the sphere, leading to a sticking without contact. The initial dynamics is described using similarity solutions, resulting in a nonlinear adhesion force that grows in time as F ~ t^(2/3). When elastic displacements become large enough, another similarity solution emerges that leads to a violent snap-off of the adhesive contact through a finite-time singularity. The observed phenomenology bears a strong resemblance with JKR theory, and is relevant for a wide range of applications involving viscous adhesion.

cond-mat.soft↗

arXiv2024

Soft Condensation

When moist air meets a cold surface, it creates a breath figure characterized by numerous small droplets. The central question is how the vapor flux is distributed between the growth of previously condensed drops and the nucleation of new ones. Here, we investigate the nucleation, growth, and coalescence of droplets on soft crosslinked polymer networks. The number of droplets initially remains constant, until drops start to coarsen according to a universal law; both phenomena are explained via the formation of a saturated boundary layer. Although nucleation occurs at a scale where the polymer network resembles a melt, we quantitatively unveil an algebraic sensitivity of the number of droplets on the substrate elasticity. Our findings suggest that nucleation follows a surprisingly low-energy pathway, influenced by the degree of crosslinking. Consequently, breath figures offer a macroscopic approach to probe the molecular characteristics of the polymer interface.

physics.flu-dyn↗

arXiv2024

Viscoelastic wetting: Cox-Voinov theory with normal stress effects

The classical Cox-Voinov theory of contact line motion provides a relation between the macroscopically observable contact angle, and the microscopic wetting angle as a function of contact line velocity. Here we investigate how viscoelasticity, specifically the normal stress effect, modifies wetting dynamics. Using the thin film equation for the second-order fluid, it is found that the normal stress effect is dominant at small scales. We show that the effect can be incorporated in the Cox-Voinov theory through an apparent microscopic angle, which differs from the true microscopic angle. The theory is applied to the classical problems of drop spreading and dip-coating, which shows how normal stress facilitates (inhibits) the motion of advancing (receding) contact lines. For rapid advancing motion, the apparent microscopic angle can tend to zero in which case the dynamics is described by a new regime that was already anticipated in Boudaoud (2007).

physics.flu-dyn↗

arXiv2024

Wetting ridge dissipation at large deformations

Liquid drops slide more slowly over soft, deformable substrates than over rigid solids. This phenomenon can be attributed to the viscoelastic dissipation induced by the moving wetting ridge, which inhibits a rapid motion, and is called "viscoelastic braking". Experiments on soft dynamical wetting have thus far been modelled using linear theory, assuming small deformations, which captures the essential scaling laws. Quantitatively, however, some important disparities have suggested the importance of large deformations induced by the sliding drops. Here we compute the dissipation occurring below a contact line moving at constant velocity over a viscoelastic substrate, for the first time explicitly accounting for large deformations. It is found that linear theory becomes inaccurate especially for thin layers, and we discuss our findings in the light of recent experiments.

cond-mat.soft↗

arXiv2023

Pressure anisotropy in polymer brushes and its effects on wetting

Polymer brushes, coatings consisting of densely grafted macromolecules, experience an intrinsic lateral compressive pressure, originating from chain elasticity and excluded volume interactions. This lateral pressure complicates a proper definition of the interface and, thereby, the determination and interpretation of the interfacial tension and its relation to the wetting behavior of brushes. Here, we study the link between grafting-induced compressive lateral pressure in polymer brushes, interfacial tension, and brush wettability using coarse-grained molecular dynamics simulations. We focus on grafting densities and polymer-liquid affinities such that the polymer and liquid do not tend to mix. For these systems, a central result is that the liquid contact angle is independent of the grafting density, which implies that the grafting-induced lateral compressive pressure in the brush does not influence its wettability. Although the definition of brush interfacial tensions is complicated by the grafting-induced pressure, the difference in interfacial tension between wet and dry brushes is perfectly well-defined. We confirm explicitly from Young's law that this difference offers an accurate description of the brush wettability. We then explore a method to isolate the grafting-induced contribution to the lateral pressure, assuming the interfacial tension to be independent of grafting density. This scenario indeed allows to disentangle interfacial and grafting effects for a broad range of parameters, except close to the mixing point. We separately discuss the latter case in the light of autophobic dewetting.

cond-mat.soft↗

arXiv2023

A unifying Rayleigh-Plesset-type equation for bubbles in viscoelastic media

Understanding the ultrasound pressure-driven dynamics of microbubbles confined in viscoelastic materials is relevant for multiple biomedical applications, ranging from contrast-enhanced ultrasound imaging to ultrasound-assisted drug delivery. The volumetric oscillations of spherical bubbles is analyzed using the Rayleigh-Plesset equation, which describes the conservation of mass and momentum in the surrounding medium. Several studies have considered an extension of the Rayleigh-Plesset equation for bubbles embedded into viscoelastic media, but these are restricted to a particular choice of constitutive model and/or to small deformations. Here, we derive a unifying equation applicable to bubbles in viscoelastic media with arbitrary complex moduli and that can account for large bubble deformations. To derive this equation, we borrow concepts from finite-strain theory. We validate our approach by comparing the result of our model to previously published results and extend it to show how microbubbles behave in arbitrary viscoelastic materials. In particular, we use our viscoelastic Rayleigh-Plesset model to compute the bubble dynamics in benchmarked viscoelastic liquids and solids.

physics.flu-dyn↗

arXiv2023

Coalescence of elastic blisters filled with a viscous fluid

Pockets of viscous fluid coalescing beneath an elastic plate are encountered in a wide range of natural phenomena and engineering processes, spanning across scales. As the pockets merge, a bridge is formed with a height increasing as the plate relaxes. We study the spatiotemporal dynamics of such an elasto-hydrodynamic coalescence process by combining experiments, lubrication theory and numerical simulations. The bridge height exhibits an exponential growth with time, which corresponds to a self-similar solution of the bending-driven thin-film equation. We address this unique self-similarity and the self-similar shape of the bridge, both of which are corroborated in numerical simulations and experiments.

physics.flu-dyn↗

arXiv2023

Coalescence of bubbles in a viscoelastic liquid

When two bubbles submerged in a liquid are brought closely together, the intermediate liquid film separating the bubbles begins to drain. Once the film ruptures, the bubbles coalesce and form a neck that expands with time. The dynamics of the neck growth are well understood in the context of pure, Newtonian liquids. Yet, much less is known about the dynamics of this singularity when the surrounding liquid contains long flexible polymers, which provide viscoelastic characteristics to the liquid's properties. Here, we experimentally study the coalescence of bubbles surrounded by polymer solutions. In contrast to drop coalescence, and in spite of the singular stretching of polymers, we find that the presence of the dissolved polymers does not at all affect the coalescence dynamics at early times. The polymer elasticity is found to slow down the flow only during the later stages of coalescence. These observations are interpreted using an asymptotic solution of the Oldroyd-B model, which predicts a strong stress singularity near the extremity of the neck. However, the polymer stress turns out to diverge only in the azimuthal direction, which can explain why elastic effects remain subdominant during the initial stages of coalescence.

physics.flu-dyn↗

arXiv2022

Drop impact on viscous liquid films

When a liquid drop falls on a solid substrate, the air layer in between them delays the occurrence of liquid--solid contact. For impacts on smooth substrates, the air film can even prevent wetting, allowing the drop to bounce off with dynamics identical to that observed for impacts on superamphiphobic materials. In this article, we investigate similar bouncing phenomena, occurring on viscous liquid films, that mimic atomically smooth substrates, with the goal to probe their effective repellency. We elucidate the mechanisms associated to the bouncing to non-bouncing (floating) transition using experiments, simulations, and a minimal model that predicts the main characteristics of drop impact, the contact time, and the coefficient of restitution. In the case of highly viscous or very thin films, the impact dynamics is not affected by the presence of the viscous film. Within this substrate--independent limit, bouncing is suppressed once the drop viscosity exceeds a critical value as on superamphiphobic substrates. For thicker or less viscous films, both the drop and film properties influence the rebound dynamics and conspire to inhibit bouncing above a critical film thickness. This substrate--dependent regime also admits a limit, for low viscosity drops, in which the film properties alone determine the limits of repellency.

physics.flu-dyn↗

arXiv2022

Reversal of Solvent Migration in Poroelastic Folds

Polymer networks and biological tissues are often swollen by a solvent, such that their properties emerge from a coupling between swelling and elastic stress. This poroelastic coupling becomes particularly intricate in wetting, adhesion, and creasing, for which sharp folds appear that can even lead to phase separation. Here we resolve the singular nature of poroelastic surface folds and determine the solvent distribution in the vicinity of the fold-tip. Surprisingly, two opposite scenarios emerge depending on the angle of the fold. In obtuse folds such as creases, it is found that the solvent is completely expelled near the crease-tip, according to a nontrivial spatial distribution. For wetting ridges with acute fold angles, the solvent migration is reversed as compared to creasing, and the degree of swelling is maximal at the fold-tip. We discuss how our poroelastic fold-analysis offers an explanation for phase separation, fracture and contact angle hysteresis.

cond-mat.soft↗

arXiv2022

Rapid Viscoelastic Spreading

We investigate the rapid spreading dynamics of a viscoelastic drop on a solid. Upon contact, surface tension drives a fast motion of the contact line along the substrate. Here, we resolve this motion for viscoelastic liquids by experiments on aqueous polymer solutions of varying concentration. It is found that while the contact line motion is only mildly affected by the polymers, the interface profile becomes much sharper owing to singular polymer stress. This behaviour is reminiscent of that observed for viscoelastic drop coalescence; in this light we revisit the analogy between spreading and coalescence, which sheds new light also on the spreading of Newtonian liquids.

physics.flu-dyn↗