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Thomas Salez

Publications and source records attributed to Thomas Salez.

At least 37 records · Page 2Linked to original sources

Swelling and evaporation determine surface morphology of grafted hydrogel thin films

We experimentally study the formation of surface patterns in grafted hydrogel films of nanometer-to-micrometer thicknesses during imbibition-driven swelling followed by evaporation-driven shrinking. Creases are known to form at the hydrogel surface during swelling; the wavelength of the creasing pattern is proportional to the initial thickness of the hydrogel film with a logarithmic correction that depends on microscopic properties of the hydrogel. We find that, although the characteristic wavelength of the pattern is determined during swelling, the surface morphology can be significantly influenced by evaporation-induced shrinking. We observe that the elastocapillary length based on swollen mechanical properties gives a threshold thickness for a surface pattern formation, and consequently an important change in morphology.

cond-mat.soft↗

The Soft-Membrane Surface Forces Apparatus

Compliant walls are widespread in biological and engineering systems. Because of their singular nature, adapted tools are required to accurately study their rheological properties as well as the consequences of the latter within a given mechanical setting. Because of their slender nature, membranes can be considered as prototypical examples of highly compliant boundaries. In this study, we describe a modified Surface Forces Apparatus (SFA) developed to measure the forces acting on a compliant membrane by measuring its deformation field. We discuss how such a device can be used to characterize the rheology of suspended membranes and accurately measure the electrostatic interactions between a polarized membrane and a spherical electrode, without the need of an external measurement spring.

cond-mat.soft↗

Bidirectional Mamba state-space model for anomalous diffusion

Characterizing anomalous diffusion is crucial in order to understand the evolution of complex stochastic systems, from molecular interactions to cellular dynamics. In this work, we characterize the performances regarding such a task of Bi-Mamba, a novel state-space deep-learning architecture articulated with a bidirectional scan mechanism. Our implementation is tested on the AnDi-2 challenge datasets among others. Designed for regression tasks, the Bi-Mamba architecture infers efficiently the effective diffusion coefficient and anomalous exponent from single, short trajectories. As such, our results indicate the potential practical use of the Bi-Mamba architecture for anomalousdiffusion characterization.

cond-mat.soft↗

Taylor's swimming sheet near a soft boundary

In 1951, G.I. Taylor modeled swimming microorganisms by hypothesizing an infinite sheet in 2D moving in a viscous medium due to a wave passing through it. This simple model not only captured the ability of microorganisms to swim due to the wavy motion of a flagella, but further development into the model captured the optimal nature of metachronal waves observed in ciliates. While the additional effects of nearby rigid boundaries and complex environments have been addressed, herein we explore the correction induced by a nearby soft boundary. Our simple model allows us to show that the magnitude of the swimming velocity gets modified near soft boundaries, and reduces for transverse waves while it increases for longitudinal waves. We further delve into the energetics of the process and the deformation of the corresponding soft boundary, highlighting the synchronization of the oscillations induced on the soft boundary with the waves passing through the sheet and the corresponding changes to the power exerted on the fluid.

cond-mat.soft↗

Singular viscoelastic perturbation to soft lubrication

Soft lubrication has been shown to drastically affect the mobility of an object immersed in a viscous fluid in the vicinity of a purely elastic wall. In this theoretical study, we develop a minimal model incorporating viscoelasticity, carrying out a perturbation analysis in both the elastic deformation of the wall and its viscous damping. Our approach reveals the singular-perturbation nature of viscoelasticity to soft lubrication. Numerical resolution of the resulting non-linear, singular and coupled equations of motion reveals peculiar effects of viscoelasticity on confined colloidal mobility, opening the way towards the description of complex migration scenarios near realistic polymeric substrates and biological membranes.

cond-mat.soft↗

Tuning the water intrinsic permeability of PEGDA hydrogel membranes by adding free PEG chains of varying molar masses

We explore the effect of poly (ethylene glycol) (PEG) molar mass on the intrinsic permeability and structural characteristics of poly (ethylene glycol) diacrylate PEGDA/PEG composite hydrogel membranes. We observe that by varying the PEG content and molar mass, we can finely adjust the water intrinsic permeability over several orders of magnitude. Notably, we show the existence of a maximum water intrinsic permeability, already identified in a previous study to be located at the critical overlap concentration C^* of PEG chains, for the highest PEG molar mass studied. Furthermore, we note that the maximum intrinsic permeability follows a non-monotonic evolution with respect to the PEG molar mass and reaches its peak at 35 000 g.mol-1. Besides our results show that a significant fraction of PEG chains is irreversibly trapped within the PEGDA matrix even for the shortest molar masses down to 600 g.mol-1. This observation suggests the possibility of covalent grafting of PEG chains to the PEGDA matrix. CryoSEM and AFM measurements demonstrate the presence of large micron-sized cavities separated by PEGDA-rich walls whose nanometric structure strongly depends on the PEG content. By combining our permeability and structural measurements, we suggest that the PEG chains trapped inside the PEGDA rich walls induce nanoscale defects in the cross linking density, resulting in an increased permeability below C^*. Conversely, above C^*, we speculate that partially-trapped PEG chains may form a brush-like arrangement on the surface of the PEGDA-rich walls, leading to a reduction in permeability. These two opposing effects are anticipated to exhibit molar-mass-dependent trends, contributing to the non-monotonic variation of the maximum intrinsic permeability at C^*. Overall, our results demonstrate the potential to fine-tune the properties of hydrogel membranes, offering new opportunities in separation applications.

cond-mat.soft↗

Direct measurement of the viscocapillary lift force near a liquid interface

Lift force of viscous origin is widespread across disciplines, from mechanics to biology. Here, we present the first direct measurement of the lift force acting on a particle moving in a viscous fluid along the liquid interface that separates two liquids. The force arises from the coupling between the viscous flow induced by the particle motion and the capillary deformation of the interface. The measurements show that the lift force increases as the distance between the sphere and the interface decreases, reaching saturation at small distances. The experimental results are in good agreement with the model and numerical calculation developed within the framework of the soft lubrication theory.

cond-mat.soft↗

Observation of Brownian elastohydrodynamic forces acting on confined soft colloids

Confined motions in complex environments are ubiquitous in microbiology. These situations invariably involve the intricate coupling between fluid flow, soft boundaries, surface forces and fluctuations. In the present study, such a coupling is investigated using a novel method combining holographic microscopy and advanced statistical inference. Specifically, the Brownian motion of softmicrometric oil droplets near rigid walls is quantitatively analyzed. All the key statistical observables are reconstructed with high precision, allowing for nanoscale resolution of local mobilities and femtonewton inference of conservative or non-conservative forces. Strikingly, the analysis reveals the existence of a novel, transient, but large, soft Brownian force. The latter might be of crucial importance for microbiological and nanophysical transport, target finding or chemical reactions in crowded environments, and hence the whole life machinery.

cond-mat.soft↗

Capillary-lubrication force between rotating cylinders separated by a fluid interface

Two cylinders rotating next to each other generate a large hydrodynamic force if the intermediate space is filled with a viscous fluid. Herein, we explore the case where the cylinders are separated by two layers of viscous immiscible fluids, in the limit of small capillary deformation of the fluid interface. As the interface deformation breaks the system's symmetry, a novel force characteristic of soft lubrication is generated. We calculate this capillary-lubrication force, which is split into velocity-dependant and acceleration-dependant contributions. Furthermore, we analyze the variations induced by modifying the viscosity ratio between the two fluid layers, their thickness ratio, and the Bond number. Unlike standard elastic cases, where a repelling soft-lubrication lift force has been abundantly reported, the current fluid bilayer setting can also exhibit an attractive force due to the non-monotonic deflection of the fluid interface when varying the sublayer thickness. Besides, at high Bond numbers, the system's response becomes analogous to the one of a Winkler-like substrate with a viscous flow inside.

cond-mat.soft↗

Growth of membranes formed by associating polymers at interfaces

Polymer association at liquid-liquid interfaces is a promising way to spontaneously obtain soft self-healing membranes. In the case of reversible bonding between two polymers, the macromolecules are mobile everywhere within the membrane and they can be absorbed into it at both boundaries due to binding to macromolecules of the other type. In this work, we develop the theoretical model of membrane growth based on these assumptions. The asymptotic dependence of membrane thickness on time as h ~ t^(1/2), as typically observed in experiments in a stationary regime, reveals an interdiffusion-controlled process, where the polymer fluxes sustain the polymer absorption at the membrane boundaries. The membrane growth rate is mainly determined by the difference in equilibrium compositions at the boundaries, the association constant, the polymer lengths and mobilities. This model is further used to describe the growth of hydrogel membranes formed via H-bonding of polymers at the interface between a solution of poly(propylene oxide) (PPO) in isopropyl myristate and an aqueous solution of poly(methacrylic acid) (PMAA). The film thickness is measured by reflectometric methods. The dependence of thickness on time can be approximated by the power law t^(beta), where beta= 1/2 for the PMAA solution at pH=3 and decreases with increasing pH and, hence, ionization degree. The growth rate slows down about 25 times for 500-nm-thick films at pH = 5.1 compared to the case of pH = 3. The ionization degree of PMAA solutions was studied by potentiometric methods. Even a small change in ionization was found to influence the growth rate of the film. A slowdown of the film growth for the ionized polymer can be explained by a drop in the composition gradient in the membrane, as is predicted by the proposed model.

cond-mat.soft↗

Plateau-Rayleigh instability of a viscous film on a soft fiber

We theoretically study the Plateau-Rayleigh instability of a thin viscous film covering a fiber consisting of a rigid cylindrical core coated with a thin compressible elastic layer. We develop a soft-lubrication model, combining the capillary-driven flow in the viscous film to the elastic deformation of the soft coating, within the Winkler-foundation framework. We perform a linear-stability analysis and derive the dispersion relation. We find that the growth rate is larger when the soft coating is more compliant. As such, softness acts as a destabilising factor. In contrast, increasing the thickness of the soft coating reduces the growth rate, due to the dominating geometrical effect.

cond-mat.soft↗

Measurement of the depth-dependent local dynamics in thin polymer films through rejuvenation of ultrastable glasses

We measure the isothermal rejuvenation of stable glass films of poly(styrene) and poly(methylmethacrylate). We demonstrate that the propagation of the front responsible for the transformation to a supercooled-liquid state can serve as a highly localized probe of the local supercooled dynamics. We use this connection to probe the depth-dependent relaxation rate with nanometric precision for a series of polystyrene films over a range of temperatures near the bulk glass transition temperature. The analysis shows the spatial extent of enhanced surface mobility and reveals the existence of an unexpected large dynamical length scale in the system. The results are compared with the cooperative-string model for glassy dynamics. The data reveals that the film-thickness dependence of whole film properties arises only from the volume fraction of the near-surface region. While the dynamics at the middle of the samples shows the expected bulk-like temperature dependence, the near-surface region shows very little dependence on temperature.

cond-mat.soft↗

Lift at low Reynolds number

Lift forces are widespread in hydrodynamics. These are typically observed for big and fast objects, and are often associated with a combination of fluid inertia (i.e. large Reynolds numbers) and specific symmetry-breaking mechanisms. In contrast, the properties of viscosity-dominated (i.e. low Reynolds numbers) flows make it more difficult for such lift forces to emerge. However, the inclusion of boundary effects qualitatively changes this picture. Indeed, in the context of soft and biological matter, recent studies have revealed the emergence of novel lift forces generated by boundary softness, flow gradients and/or surface charges. The aim of the present review is to gather and analyse this corpus of literature, in order to identify and unify the questioning within the associated communities, and pave the way towards future research.

cond-mat.soft↗

Sieving and clogging in PEG-PEGDA hydrogel membranes

Hydrogels are promising systems for separation applications due to their structural characteristics (i.e. hydrophilicity and porosity). In our study, we investigate the permeation of suspensions of rigid latex particles of different sizes through free-standing hydrogel membranes prepared by photopolymerization of a mixture of poly (ethylene glycol) diacrylate (PEGDA) and large poly (ethylene glycol) (PEG) chains of 300 000 g.mol-1 in the presence of a photoinitiator. Atomic force microscopy (AFM) and cryoscanning electron microscopy (cryoSEM) were employed to characterize the structure of the hydrogel membranes. We find that the 20 nm particle permeation depends on both the PEGDA/PEG composition and the pressure applied during filtration. In contrast, we do not measure a significant permeation of the 100 nm and 1 $μ$m particles, despite the presence of large cavities of 1 $μ$m evidenced by cryoSEM images. We suggest that the PEG chains induce local nanoscale defects in the cross-linking of PEGDA-rich walls separating the micron size cavities, that control the permeation of particles and water. Moreover, we discuss the decline of the permeation flux observed in the presence of latex particles, compared to that of pure water. We suggest that a thin layer of particles forms on the surface of the hydrogels.

cond-mat.soft↗

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↗

Unsteady drag force on an immersed sphere oscillating near a wall

The unsteady hydrodynamic drag exerted on an oscillating sphere near a planar wall is addressed experimentally, theoretically, and numerically. The experiments are performed by using colloidal-probe Atomic Force Microscopy (AFM) in thermal noise mode. The natural resonance frequencies and quality factors are extracted from the measurement of the power spectrum density of the probe oscillation for a broad range of gap distances and Womersley numbers. The shift in the natural resonance frequency of the colloidal probe as the probe goes close to a solid wall infers the wall-induced variations of the effective mass of the probe. Interestingly, a crossover from a positive to a negative shift is observed as the Womersley number increases. In order to rationalize the results, the confined unsteady Stokes equation is solved numerically using a finite-element method, as well as asymptotic calculations.The in-phase and out-of-phase terms of the hydrodynamic drag acting on the sphere are obtained and agree well to the experimental results. All together, the experimental, theoretical, and numerical results show that the hydrodynamic force felt by an immersed sphere oscillating near a wall is highly dependent on the Womersley number.

cond-mat.soft↗

Instability and rupture of sheared viscous liquid nanofilms

Liquid nanofilms are ubiquitous in nature and technology, and their equilibrium and out-of-equilibrium dynamics are key to a multitude of phenomena and processes. We numerically study the evolution and rupture of viscous nanometric films, incorporating the effects of surface tension, van der waals forces, thermal fluctuations and viscous shear. We show that thermal fluctuations create perturbations that can trigger film rupture, but they do not significantly affect the growth rate of the perturbations. The film rupture time can be predicted from a linear stability analysis of the governing thin film equation, by considering the most unstable wavelength and the thermal roughness. Furthermore, applying a sufficiently large unidirectional shear can stabilise large perturbations, creating a finite-amplitude travelling wave instead of film rupture. In contrast, in three dimensions, unidirectional shear does not inhibit rupture, as perturbations are not suppressed in the direction perpendicular to the applied shear. However, if the direction of shear varies in time, the growth of large perturbations is prevented in all directions, and rupture can hence be impeded.

cond-mat.soft↗

Capillary-lubrication force exerted on a 2D particle moving towards a fluid interface

A rigid object moving in a viscous fluid and in close proximity with an elastic wall experiences self-generated elastohydrodynamic interactions. This has been the subject of an intense research activity, with a recent and growing attention given to the particular case of elastomeric and gel-like substrates. Here, we address the situation where the elastic wall is replaced by a capillary surface. Specifically, we analyze the lubrication flow generated by the prescribed normal motion of a rigid infinite cylinder near the deformable interface separating two immiscible and incompressible viscous fluids. Using a combination of analytical and numerical treatments, we compute the emergent capillary-lubrication force at leading order in compliance, and characterize its dependencies with the interfacial tension, viscosities of the fluids, and length scales of the problem. Interestingly, we identify two main contributions: i) a velocity-dependent adhesion-like force ; ii) an acceleration-dependant inertial-like force. Our results may have implications for the mobility of colloids near complex interfaces and for the motility of confined microbiological entities.

cond-mat.soft↗