arXiv subjects

Jacco H. Snoeijer

Publications and source records attributed to Jacco H. Snoeijer.

At least 37 records · Page 2Linked to original sources

arXiv2022

The asymmetric coalescence of two droplets with different surface tensions is caused by capillary waves

When two droplets with different surface tensions collide, the shape evolution of the merging droplets is asymmetric. Using experimental and numerical techniques, we reveal that this asymmetry is caused by asymmetric capillary waves, which are the result of the different surface tensions of the droplets. We show that the asymmetry is enhanced by increasing the surface tension difference, and suppressed by increasing the inertia of the colliding droplets. Furthermore, we study capillary waves in the limit of no inertia. We reveal that the asymmetry is not directly caused by Marangoni forces. In fact, somehow counterintuitive, asymmetry is strongly reduced by the Marangoni effect. Rather, the different intrinsic capillary wave amplitudes and velocities associated with the different surface tensions of the droplets lie at the origin of the asymmetry during droplet coalescence.

physics.flu-dyn↗

arXiv2021

A thin-film equation for a viscoelastic fluid, and its application to the Landau-Levich problem

Thin-film flows of viscoelastic fluids are encountered in various industrial and biological settings. The understanding of thin viscous film flows in Newtonian fluids is very well developed, which for a large part is due to the so-called thin-film equation. This equation, a single partial differential equation describing the height of the film, is a significant simplification of the Stokes equation effected by the lubrication approximation which exploits the thinness of the film. There is no such established equation for viscoelastic fluid flows. Here we derive the thin-film equation for a second-order fluid, and use it to study the classical Landau-Levich dip-coating problem. We show how viscoelasticity of the fluid affects the thickness of the deposited film, and address the discrepancy on the topic in literature.

physics.flu-dyn↗

arXiv2021

Non-wetting drop dynamics

The impact of droplets on solids or weakly-deformable surfaces can lead to non-wetting outcomes, depending on the control parameters. Here, we perform experiments and develop a simple model to understand the impact dynamics by varying three important drop parameters: the Ohnesorge number $\mathcal{O}h$, the Bond number $\mathcal{B}o$ and the Weber number $\mathcal{W}e$. The model suggests that the droplet dynamics is captured by only two non-dimensional groups, namely $\ \mathcal{O}h$ and $ξ= \mathcal{B}o/\sqrt{\mathcal{W}e}$. For $ξ\ll 1$, the droplet dynamics is fully dominated by $\mathcal{O}h$, but for $ξ\gg 1$, the dynamics depends both on $\mathcal{O}h$ and $ξ$. While the model results show some discrepancies for small $\mathcal{O}h$, they are in very good agreement with the experiments for moderately large $\mathcal{O}h$. The work thereby offers an elaborate description of the droplet impact dynamics in a non-wetting scenario.

physics.flu-dyn↗

arXiv2021

The retraction of jetted slender viscoelastic liquid filaments

Long and slender liquid filaments are produced during inkjet printing, which can subsequently either retract to form a single droplet, or break up to form a primary droplet and one or more satellite droplets. These satellite droplets are undesirable since they degrade the quality and reproducibility of the print. Existing strategies for the suppression of satellite droplet formation include, among others, adding viscoelasticity to the ink. In the present work, we aim to improve the understanding of the role of viscoelasticity in suppressing satellite droplets in inkjet printing. We demonstrate that very dilute viscoelastic aqueous solutions (concentrations $\sim$ 0.003\% wt. polyethylene oxide (PEO), corresponding to nozzle Deborah number $De_{n}$ $\sim$ 3) can suppress satellite droplet formation. Furthermore, we show that, for a given driving condition, upper and lower bounds of polymer concentration exist, within which satellite droplets are suppressed. Satellite droplets are formed at concentrations below the lower bound, while jetting ceases for concentrations above the upper bound (for fixed driving conditions). Moreover, we observe that, with concentrations in between the two bounds, the filaments retract at velocities larger than the corresponding Taylor-Culick velocity for the Newtonian case. We show that this enhanced retraction velocity can be attributed to the elastic tension due to polymer stretching, which builds up during the initial jetting phase. These results shed some light on the complex interplay between inertia, capillarity, and viscoelasticity for retracting liquid filaments, which is important for the stability and quality of inkjet printing of polymer solutions.

physics.flu-dyn↗

arXiv2021

Gradient-dynamics model for liquid drops on elastic substrates

The wetting of soft elastic substrates exhibits many features that have no counterpart on rigid surfaces. Modelling the detailed elastocapillary interactions is challenging, and has so far been limited to single contact lines or single drops. Here we propose a reduced long-wave model that captures the main qualitative features of statics and dynamics of soft wetting, but which can be applied to ensembles of droplets. The model has the form of a gradient dynamics on an underlying free energy that reflects capillarity, wettability and compressional elasticity. With the model we first recover the double transition in the equilibrium contact angles that occurs when increasing substrate softness from ideally rigid towards very soft (i.e., liquid). Second, the spreading of single drops of partially and completely wetting liquids is considered showing that known dependencies of the dynamic contact angle on contact line velocity are well reproduced. Finally, we go beyond the single droplet picture and consider the coarsening for a two-drop system as well as for a large ensemble of drops. It is shown that the dominant coarsening mode changes with substrate softness in a nontrivial way.

physics.flu-dyn↗

arXiv2021

When elasticity affects drop coalescence

The breakup and coalescence of drops are elementary topological transitions in interfacial flows. The breakup of a drop changes dramatically when polymers are added to the fluid. With the strong elongation of the polymers during the process, long threads connecting the two droplets appear prior to their eventual pinch-off. Here, we demonstrate how elasticity affects drop coalescence, the complement of the much studied drop pinch-off. We reveal the emergence of an elastic singularity, characterised by a diverging interface curvature at the point of coalescence. Intriguingly, while the polymers dictate the \emph{spatial} features of coalescence, they hardly affect the \emph{temporal} evolution of the bridge. These results are explained using a novel viscoelastic similarity analysis and are relevant for drops created in biofluids, coating sprays and inkjet printing.

physics.flu-dyn↗

arXiv2021

Theory for the coalescence of viscous lenses

Drop coalescence occurs through the rapid growth of a liquid bridge that connects the two drops. At early times after contact, the bridge dynamics is typically self-similar, with details depending on the geometry and viscosity of the liquid. In this paper we analyse the coalescence of two-dimensional viscous drops that float on a quiescent deep pool; such drops are called liquid lenses. The analysis is based on the thin-sheet equations, which were recently shown to accurately capture experiments of liquid lens coalescence. It is found that the bridge dynamics follows a self-similar solution at leading order, but, depending on the large-scale boundary conditions on the drop, significant corrections may arise to this solution. This dynamics is studied in detail using numerical simulations and through matched asymptotics. We show that the liquid lens coalescence can involve a global translation of the drops, a feature that is confirmed experimentally.

physics.flu-dyn↗

arXiv2021

Pinning-induced folding-unfolding asymmetry in adhesive creases

The compression of soft elastic matter and biological tissue can lead to creasing, an instability where a surface folds sharply into periodic self-contacts. Intriguingly, the unfolding of the surface upon releasing the strain is usually not perfect: small scars remain that serve as nuclei for creases during repeated compressions. Here we present creasing experiments with sticky polymer surfaces, using confocal microscopy, which resolve the contact line region where folding and unfolding occurs. It is found that surface tension induces a second fold, at the edge of the self-contact, which leads to a singular elastic stress and self-similar crease morphologies. However, these profiles exhibit an intrinsic folding-unfolding asymmetry that is caused by contact line pinning, in a way that resembles wetting of liquids on imperfect solids. Contact line pinning is therefore a key element of creasing: it inhibits complete unfolding and gives soft surfaces a folding memory.

cond-mat.soft↗

arXiv2021

How to unloop a self-adherent sheet

The mechanics of adherent sheets is central to applications ranging from patching a band aid, coating technology, to the breakthrough discovery of peeling graphene flakes using sticky tape. These processes are often hindered by the formation of blisters and loops, which are notoriously difficult to remove. Here we describe and explain a remarkable phenomenon that arises when one attempts to remove a loop in a self-adherent sheet that is formed by, e.g., folding two adhesive sides of a tape together. One would expect the loop to simply unloop when pulling on its free ends. Surprisingly, however, the loop does not immediately open up but shrinks in size, held together by a tenuous contact region that propagates along the tape. This adhesive contact region only ruptures once the loop is reduced to a critical size. We experimentally show that the loop-shrinkage results from an interaction between the peeling front and the loop, across the contact zone. This new type of interaction falls outside the realm of the classical elastica theory and is responsible for a highly nonlinear increase in the peeling force. Our results reveal and quantify the increased force required to remove loops in self-adherent media, which is of importance for blister removal and exfoliation of graphene sheets.

cond-mat.soft↗

arXiv2020

Elastic Rayleigh-Plateau instability: Dynamical selection of nonlinear states

A slender thread of elastic hydrogel is susceptible to a surface instability that is reminiscent of the classical Rayleigh-Plateau instability of liquid jets. The final, highly nonlinear states that are observed in experiments arise from a competition between capillarity and large elastic deformations. Combining a slender analysis and fully three-dimensional numerical simulations, we present the phase map of all possible morphologies for an unstable neo-Hookean cylinder subjected to capillary forces. Interestingly, for softer cylinders we find the coexistence of two distinct configurations, namely, cylinders-on-a-string and beads-on-a-string. It is shown that for a given set of parameters, the final pattern is selected via a dynamical evolution. To capture this, we compute the dispersion relation and determine the characteristic wavelength of the dynamically selected profiles. The validity of the "slender" results is confirmed via simulations and these results are consistent with experiments on elastic and viscoelastic threads.

cond-mat.soft↗

arXiv2020

Desorption energy of soft particles from a fluid interface

The efficiency of soft particles to stabilize emulsions is examined by measuring their desorption free energy, i.e., the mechanical work required to detach the particle from a fluid interface. Here, we consider rubber-like elastic as well as microgel particles, using coarse-grained molecular dynamics simulations. The energy of desorption is computed for two and three-dimensional configurations by means of the mean thermodynamic integration method. It is shown that the softness affects the particle-interface binding in two opposing directions as compared to rigid particles. On the one hand, a soft particle spreads at the interface and thereby removes a larger unfavorable liquid-liquid contact area compared to rigid particles. On the other hand, softness provides the particle with an additional degree of freedom to get reshaped instead of deforming the interface, resulting in a smaller restoring force during the detachment. It is shown that the first effect prevails so that a soft spherical particle attaches to the fluid interface more strongly than rigid spheres. Finally, we consider microgel particles both in the swollen and in the collapsed state. Surprisingly, we find that the latter has a larger binding energy. All results are rationalised using thermodynamic arguments and thereby offer detailed insights into the desorption energy of soft particles from fluid interfaces.

cond-mat.soft↗

arXiv2020

Initial solidification dynamics of spreading droplets

When a droplet is brought in contact with an undercooled surface, it wets the substrate and solidifies at the same time. The interplay between the phase transition effects and the contact-line motion, leading to its arrest, remains poorly understood. Here we reveal the early solidification patterns and dynamics of spreading hexadecane droplets. Total internal reflection (TIR) imaging is employed to temporally and spatially resolve the early solidification behaviour. With this, we determine the conditions leading to the contact-line arrest. We quantify the overall nucleation behaviour, \textit{i.e.} the nucleation rate and the crystal growth speed, and show its sensitivity to the applied undercooling of the substrate. By combining the Johnson-Mehl-Avrami-Kolmogorov nucleation theory and scaling relations for the spreading, we can calculate the temporal evolution of the solid area fraction, which is in good agreement with our observations. We also show that for strong enough undercooling it is the rapid growth of the crystals which determines the eventual arrest of the spreading contact line.

cond-mat.soft↗

arXiv2020

Wetting of two-component drops: Marangoni contraction versus autophobing

The wetting properties of multi-component liquids are crucial to numerous industrial applications. The mechanisms that determine the contact angles for such liquids remain poorly understood, with many intricacies arising due to complex physical phenomena, for example due to the presence of surfactants. Here, we consider two-component drops that consist of mixtures of vicinal alkane diols and water. These diols behave surfactant-like in water. However, the contact angles of such mixtures on solid substrates are surprisingly large. We experimentally reveal that the contact angle is determined by two separate mechanisms of completely different nature, namely Marangoni contraction (hydrodynamic) and autophobing (molecular). It turns out that the length of the alkyl tail of the alkane diol determines which mechanism is dominant, highlighting the intricate coupling between molecular physics and the macroscopic wetting of complex fluids.

physics.flu-dyn↗

arXiv2020

Self-Similar Liquid Lens Coalescence

A basic feature of liquid drops is that they can merge upon contact to form a larger drop. In spite of its importance to various applications, drop coalescence on pre-wetted substrates has received little attention. Here, we experimentally and theoretically reveal the dynamics of drop coalescence on a thick layer of a low-viscosity liquid. It is shown that these so-called "liquid lenses" merge by the self-similar vertical growth of a bridge connecting the two lenses. Using a slender analysis, we derive similarity solutions corresponding to the viscous and inertial limits. Excellent agreement is found with the experiments without any adjustable parameters, capturing both the spatial and temporal structure of the flow during coalescence. Finally, we consider the crossover between the two regimes and show that all data of different lens viscosities collapse on a single curve capturing the full range of the coalescence dynamics.

physics.flu-dyn↗

arXiv2019

Inverse Leidenfrost drop manipulation using menisci

Drops deposited on an evaporating liquid bath can be maintained in an inverse Leidenfrost state by the vapor emanating from the bath, making them levitate and hover almost without friction. These perfectly non-wetting droplets create a depression in the liquid interface that sustains their weight, which generates repellent forces when they approach a meniscus rising against a wall. Here, we study this reflection in detail, and show that frictionless Leidenfrost drops are a simple and efficient tool to probe the shape of an unknown interface. We then use the menisci to control the motion of the otherwise elusive drops. We create waveguides to direct and accelerate them and use parabolic walls to reflect and focus them. This could be particularly beneficial in the scale up of droplet cryopreservation processes: capillary interactions can be used to transport, gather and collect vitrified biological samples in absence of contact and contamination.

physics.flu-dyn↗

arXiv2019

Solidification of liquid metal drops during impact

Hot liquid metal drops impacting onto a cold substrate solidify during their subsequent spreading. Here we experimentally study the influence of solidification on the outcome of an impact event. Liquid tin drops are impacted onto sapphire substrates of varying temperature. The impact is visualised both from the side and from below, which provides a unique view on the solidification process. During spreading an intriguing pattern of radial ligaments rapidly solidifies from the centre of the drop. This pattern determines the late-time morphology of the splat. A quantitative analysis of the drop spreading and ligament formation is supported by scaling arguments. Finally, a phase diagram for drop bouncing, deposition and splashing as a function of substrate temperature and impact velocity is provided.

physics.flu-dyn↗

arXiv2019

Peeling an elastic film from a soft viscoelastic adhesive: experiments and scaling laws

The functionality of adhesives relies on their response under the application of a load. Yet, it has remained a challenge to quantitatively relate the macroscopic dynamics of peeling to the dissipative processes inside the adhesive layer. Here we investigate the peeling of a reversible adhesive made of a polymer gel, measuring the relationship between the peeling force, the peeling velocity, and the geometry of the interface at small-scale. Experiments are compared to a theory based on the linear viscoelastic response of the adhesive, augmented with an elastocapillary regularization approach. This theory, fully quantitative in the limit of small surface deformations, demonstrates the emergence of a "wetting" angle at the contact line and exhibits scaling laws for peeling which are in good agreement with the experimental results. Our findings provide a new strategy for design of reversible adhesives, by quantitatively combining wetting, geometry and dissipation.

cond-mat.soft↗

arXiv2019

A flexible rheometer design to measure the visco-elastic response of soft solids over a wide range of frequency

We present a flexible set-up for determining the rheology of visco-elastic materials which is based on the mechanical response of a magnet deposited at the surface of a slab of material and excited electromagnetically. An interferometric measurement of the magnet displacement allows one to reach an excellent accuracy over a wide range of frequency. Except for the magnet, there is no contact between the material under investigation and the apparatus. At low frequency, inertial effects are negligible so that the mechanical response, obtained through a lock-in amplifier, directly gives the material complex modulus. At high frequency, damped waves are emitted and the rheology must be extracted numerically from a theoretical model. To validate the design, the instrument was used to measure the rheology of a test PDMS gel which presents an almost perfect scale free response at high frequency.

cond-mat.soft↗