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Matthieu Roché

Publications and source records attributed to Matthieu Roché.

15 recordsLinked to original sources

Thin-film flows of granular suspensions on a solid surface

This review article examines the complex dynamics of thin-film flows of granular suspensions spreading over rigid solid substrates with free air interfaces. Such systems feature an involved coupling of the free-surface dynamics with the flow and microstructure of the suspension. In particular, we develop two canonical thin-film situations: drop spreading and dip-coating. In drop spreading, confinement of the particulate phase near the advancing contact line alters both the spreading rate and the interface shape. In dip-coating, understanding the entrainment of fluid and particles becomes challenging as the film thickness approaches the particle size.

cond-mat.soft

Sliding of liquid droplets on thin viscoelastic soft layers

Soft substrates are deformed by liquid-vapor surface tension upon contact with liquid droplets, forming the well-known wetting ridge. This ridge dynamically propagates with the moving contact line and critically influences liquid spreading. Here, we experimentally investigate gravity-driven sliding dynamics of water droplets on vertically tilted silicone layers whose viscoleasticity is characterized by the Chasset-Thirion model with the exponent m. At low Bond numbers, the sliding velocity scales with droplet size as V S $\sim$ D 2 m . While in the thin-film limit, velocity exhibits a pronounced power-law dependence on nominal substrate thickness, V S $\sim$ $Π$(h) -1 m . We rationalize these observations by quantifying viscoelastic dissipation within the soft layer and balancing it against the gravitational driving force using an energy-conservation framework. Our findings offer novel avenues for designing advanced soft coatings, anti-fouling and self-cleaning surfaces, and biomedical devices.

cond-mat.soft

Granular aqueous suspensions with controlled inter-particular friction and adhesion

We present a simple route to obtain large quantities of suspensions of non-Brownian particles with stimuli-responsive surface properties to study the relation between their flow and interparticle interactions. We perform an alkaline hydrolysis reaction on poly(methyl methacrylate) (PMMA) particles to obtain poly(sodium methacrylate) (PMAA-Na) particles. We characterize the quasi-static macroscopic frictional response of their aqueous suspensions using a rotating drum. The suspensions are frictionless when the particles are dispersed in pure water. We relate this state to the presence of electrosteric repulsion between the charged surfaces of the ionized PMAA-Na particles in water. Then we add monovalent and multivalent ions (Na+, Ca2+, La3+) and we observe that the suspensions become frictional whatever the valency. For divalent and trivalent ions, the quasi-static avalanche angle θc at large ionic strength is greater than that of frictional PMMA particles in water, suggesting the presence of adhesion. Finally, a decrease in the pH of the suspending solution leads to a transition between a frictionless plateau and a frictional one. We perform Atomic Force Microscopy (AFM) to relate our macroscopic observations to the surface features of the particles. In particular, we show that the increase in friction in the presence of multivalent ions or under acidic conditions is driven by a nanoscopic phase separation and the bundling of polyelectrolyte chains at the surface of the particle. Our results highlight the importance of surface interactions in the rheology of granular suspensions. Our particles provide a simple, yet flexible platform to study frictional suspension flows.

cond-mat.soft

Success and failure of the spreading law for large drops of dense granular suspensions

The spreading of large viscous drops of density-matched suspensions of non-Brownian spheres on a smooth solid surface is experimentally investigated at the global drop scale. The focus is on dense suspensions with a solid volume fraction equal to or greater than $40\%$ and for drops larger than the capillary length, i.e. for which the spreading is governed by the balance of gravitational and viscous forces. Our findings indicate that all liquids exhibit a power law behaviour typical of gravity-driven dynamics, albeit with an effective suspension viscosity that is smaller than the bulk value. When the height of the drop is of the order of the particle size, the power law breaks down as the particles freeze while the contact line continues to advance.

cond-mat.soft

Anomalous near-equilibrium capillary rise

We report and rationalize the observation of a crossover from the classical Lucas-Washburn dynamics to a long-lived anomalously slow regime for capillary rise in simple glass tubes. We propose an analytical model considering the role of thermal motion and the nanoscale surface topography to account for the experimental observations. The proposed model indicates that the contact line perimeter and the surface topography dimensions determine the crossover condition and anomalous imbibition rate. Our findings have important implications for the scientific understanding and technical application of capillary imbibition and suggest strategies to control the adsorption of specific liquids in porous materials.

cond-mat.soft

Morphology and stability of droplets sliding on soft viscoelastic substrates

We show that energy dissipation partition between a liquid and a solid controls the shape and stability of droplets sliding on viscoelastic gels. When both phases dissipate energy equally, droplet dynamics is similar to that on rigid solids. When only the solid dissipate, we observe an apparent contact angle hysteresis, of viscoelastic origin. We find excellent agreement between our data and a non-linear model of the wetting of gels of our own that also indicates the presence of significant slip. Our work opens general questions on the dynamics of curved contact lines on compliant substrates.

cond-mat.soft

Probing dissipation in spreading drops with granular suspensions

In this article, we study the spreading of droplets of density-matched granular suspensions on the surface of a solid. Bidispersity of the particle size distribution enriches the conclusions drawn from monodisperse experiments by highlighting key elements of the wetting dynamics. In all cases, the relation between the dynamic contact angle and the velocity of the contact line follows a similar relation as that of a simple fluid, despite the complexity introduced by the presence of particles. We extract from this relation an apparent wetting viscosity of the suspensions that differs from that measured in the bulk. Dimensional analysis supported by experimental measurements yields estimate of the size of the region inside the droplet where the value of the dynamic contact angle depends on a balance of viscous dissipation and capillary stresses. Depending on how particle size compares with this viscous cut-off length seems crucial in determining the value of the apparent wetting viscosity. With bimodal blends, the particle size ratio can be used to show the effects of the local structure and volume fraction at the contact line, both impacting the value of the corresponding wetting viscosity.

cond-mat.soft

Spreading of granular suspensions on a solid surface

We examine the spreading of a suspension of non-Brownian spheres suspended in a Newtonian liquid on a solid substrate. We show that the spreading dynamics is well described by the classical Cox-Voinov law provided the value of the fluid viscosity that arises in the capillary number of the problem is adjusted to a value that depends on particle size and volume fraction in a non-trivial way. We demonstrate that this behavior is a signature of the ability of the particles to approach the contact line close enough to affect dissipation.

physics.flu-dyn

Nonlinear force balance at moving contact lines

The spreading of a liquid over a solid material is a key process in a wide range of applications. While this phenomenon is well understood when the solid is undeformable, its "soft" counterpart is still ill-understood and no consensus has been reached with regards to the physical mechanisms ruling the spreading of liquid drops over soft deformable materials. In this work we show that the motion of a triple line on a soft elastomer is opposed both by nonlinear localized capillary and visco-elastic forces. We give an explicit analytic formula relating the dynamic contact angle of a moving drop with its velocity for arbitrary rheology. We then specialize this formula to the experimentally relevant case of elastomers with Chasset-Thirion (power-law) type of rheologies. The theoretical prediction are in very good agreement with experimental data, without any adjustable parameters. Finally, we show that the nonlinear force balance presented in this work can also be used to recover the classical de Gennes model of wetting.

cond-mat.soft

Corners in soft solids behave as defects in crystals

All phases of matter, solid, liquid or gas, present some excess energy, compared to their bulk, at their interfaces with other materials. This excess of energy, known as the surface energy, is a fundamental property of matter and is involved in virtually all interface problems in science, from the shape of bubbles, crystals and biological cells to the delicate motion of some insects on water or the fluttering of red blood cells. Because of their high cohesive internal energies, the surface energies of solids differ fundamentally from those of fluids and depend on the solid deformations. This effect, known as the Shuttleworth effect, is well established for metals but is highly debated for amorphous materials such as glasses, elastomers or biological tissues with recent experimental results yielding strictly opposite conclusions with regards to its very existence. Using a combination of analytical results and numerical simulations, we show in this paper that those seemingly opposite results can be reconciled due to the existence of an analog of the Peach-Koehler force acting on the elastocapillary ridge and conclude that: i) there is no large Shuttleworth effect in soft elastomers and ii) the Neumann construction does not hold in elastowetting.

cond-mat.soft

Life and death of not so "bare" bubbles

In this paper, we investigate how the drainage and rupture of surfactant-stabilised bubbles floating at the surface of a liquid pool depend on the concentration of surface-active molecules in water. Drainage measurements at the apex of bubbles indicate that the flow profile is increasingly plug-like as the surfactant concentration is decreased from several times the critical micellar concentration (cmc) to just below the cmc. High-speed observations of bubble bursting reveal that the position at which a hole nucleates in the bubble cap also depends on the surfactant concentration. On average, the rupture is initiated close to the bubble foot for low concentrations (< cmc) while its locus moves towards the top of the bubble cap as the concentration increases above the cmc. In order to explain this transition, we propose that marginal regeneration may be responsible for bubble rupture at low concentrations but that bursting at the apex for higher concentrations is driven by gravitational drainage.

cond-mat.soft

Stable freestanding thin films of copolymer melts far from the glass transition

Thin polymer films have attracted attention because of both their broad range of applications and of the fundamental questions they raise regarding the dynamic response of confined polymers. These films are unstable if the temperature is above their glass transition temperature Tg. Here, we describe freestanding thin films of centimetric dimensions made of a comb copolymer melt far from its glass transition that are stable for more than a day. These long lifetimes allowed us to characterize the drainage dynamics and the thickness profile of the films. Stratified regions appear as the film drains. We have evidence that the stability, thinning dynamics and thickness profile of the films result from structural forces in the melt. Understanding the key mechanisms behind our observations may lead to new developments in polymeric thin films, foams and emulsions without the use of stabilizing agents.

cond-mat.soft

The Marangoni flow of soluble amphiphiles

Surfactant distribution heterogeneities at a fluid/fluid interface trigger the Marangoni effect, i.e. a bulk flow due to a surface tension gradient. The influence of surfactant solubility in the bulk on these flows remains incompletely characterized. Here we study Marangoni flows sustained by injection of hydrosoluble surfactants at the air/water interface. We show that the flow extent increases with a decrease of the critical micelle concentration, i.e. the concentration at which these surfactants self-assemble in water. We document the universality of the surface velocity field and predict scaling laws based on hydrodynamics and surfactant physicochemistry that capture the flow features.

physics.flu-dyn

Nanoemulsions obtained via bubble bursting at a compound interface

The bursting of bubbles at an air/liquid interface is a familiar occurrence important to foam stability, cell cultures in bioreactors and mass transfer between the sea and atmosphere. Here we document the hitherto unreported formation and dispersal into the water column of submicrometre oil droplets following bubble bursting at a compound air/oil/water-with-surfactant interface. We show that dispersal results from the detachment of an oil spray from the bottom of the bubble towards water during bubble collapse. We provide evidence that droplet size is selected by physicochemical interactions between oil molecules and the surfactants rather than by hydrodynamic effects. We illustrate the unrecognized role that this dispersal mechanism may play in the fate of the sea surface micro-layer and of pollutant spills by dispersing petroleum in the water column. Finally, our system provides an energy-efficient route, with potential upscalability and wide applicability, for applications in drug delivery, food production and material science, which we demonstrate by producing polymeric nanoparticles.

physics.flu-dyn

Buckling dynamics of a solvent-stimulated stretched elastomeric sheet

When stretched uniaxially, a thin elastic sheet may exhibit buckling. The occurrence of buckling depends on the geometrical properties of the sheet and the magnitude of the applied strain. Here we show that an elastomeric sheet initially stable under uniaxial stretching can destabilize when exposed to a solvent that swells the elastomer. We demonstrate experimentally and computationally that the features of the buckling pattern depend on the magnitude of stretching, and this observation offers a new way for controlling the shape of a swollen homogeneous thin sheet.

cond-mat.soft