arXiv subjects

Cécile Monteux

Publications and source records attributed to Cécile Monteux.

13 recordsLinked to original sources

arXiv2026

Dripping-onto-droplet rheometry of sodium alginate solutions

In this experimental and theoretical study, we assess the extensional relaxation time of sodium alginate solutions by using dripping-onto-droplet capillary breakup rheometry (DoD), e.g., the capillary thinning and breakup of viscoelastic filaments formed following the coalescence of a millimetric-nozzle-generated pendant drop with a lower droplet cap of the same fluid contained in a millimetric pool in ambient air. Hence, we extend the analyses conducted by El Khoury et al. (2026) from Newtonian to viscoelastic fluids. Our approach relies on experiments recorded with a high-speed camera using sodium alginate in deionised water, with alginate concentrations ranging from 0.1% to 9% by weight. The results are depicted by considering the dynamics of fluid filament thinning, stress balances, and scaling laws. Extensional relaxation times are resolved from the filament diameter evolution. Three flow regimes are highlighted: capillary-inertial, capillary-elastic, and mixed capillary-inertio-elastic. The findings are summarised in a two-dimensional diagram that correlates the filament breakup time with different flow regimes using the important dimensionless parameter of the problem, e.g., the intrinsic Deborah number (which relates the extensional relaxation time to the characteristic capillary-inertial time). This diagram can be used to quantify both the solution's extensional relaxation time and the liquid/air surface tension solely from filament breakup times.

physics.flu-dyn↗

arXiv2026

Real-time quantification of fluid flows around bubbles during directional solidification

Directional solidification of bubbly liquids plays a critical role in shaping the microstructure and properties of many materials, yet the fluid dynamics governing bubble behavior during solidification remain poorly understood. Using cryo-confocal microscopy and particle image velocimetry, we quantify fluid flows around bubbles during solidification of water containing surfactants and tracers. Our results reveal that volumetric expansion dominates fluid motion, with velocities scaling linearly with the solidification rate (1-20$~μm/s$), while Marangoni flows-hypothesized to play a key role-are negligible ($< 5~μm/s$) under our experimental conditions. Diffusiophoresis and thermophoresis also contribute minimally. These findings challenge existing theoretical models and provide a framework for controlling bubble distribution in solidified materials

cond-mat.soft↗

arXiv2026

Coupled gas and bubble dynamics at the solidification front

The formation and entrapment of gas bubbles during solidification significantly influence the microstructure and mechanical properties of materials, from metallic alloys to ice. While gas segregation at the solidification front is well-documented, the real-time dynamics of bubble nucleation, growth, and engulfment-and their dependence on solidification velocity-remain poorly understood. In this study, we use in situ cryo-confocal fluorescence microscopy to investigate the coupled gas-bubble dynamics at the solidification front of carbonated water, systematically varying the solidification velocity ($V = 1-20 μm/s$) while maintaining a constant thermal gradient ($G = 15 K/mm$). Our experiments reveal that bubble nucleation is governed by a characteristic nucleation time, which emerges from the interplay between gas diffusion ahead of the front, nucleation kinetics, and bubble growth, all competing with the advancing solidification front. These results allow us to estimate the critical gas concentration for bubbles nucleation in carbonated water. These results offer a detailed understanding of the mechanisms controlling bubble nucleation and entrapment during solidification at constant thermal gradient. They contribute to the development of strategies to control bubble formation in industrial processes where the presence of bubbles can either be detrimental or intentionally harnessed.

cond-mat.soft↗

arXiv2025

pH-dependent interfacial rheology of polymer membranes assembled at liquid-liquid interfaces using hydrogen bonds

Self-assembly of polymers at liquid interfaces using non-covalent interactions has emerged as a promising technique to reversibly produce self-healing membranes. Besides the assembly process, it is also crucial to control the mechanical properties of these membranes. Here, we measure the interfacial rheological properties of PMAA-PPO (polymethacrylic acid - polypropylene oxide) polymer membranes assembled using hydrogen bonds at the interface between water and a polar oil, Mygliol. Varying the pH enables us to modify the degree of ionization of the PMAA chains, and hence their ability to establish hydrogen interactions with PPO. Frequency sweeps of the interfacial layers show a crossover between a viscous regime at low frequencies and an elastic regime at high frequencies. The crossover elastic modulus, measured one hour after the two phases were put into contact, decreases by a half over the pH range investigated, which can be accounted for by a decrease of the layer thickness as pH increases. Furthermore, we find that the crossover frequency varies exponentially with the degree of ionization of PMAA. To account for these observations, we propose a simple picture where the short PPO chains behave as non-covalent cross-linkers that bridge several PMAA chains. The dissociation rate and hence the crossover frequency are controlled by the number of PO units per PPO chain involved in the hydrogen bonds.

cond-mat.soft↗

arXiv2025

Gelation effects on the spreading of non-Newtonian drops impacting a reactive liquid

We report in this experimental and numerical study effects of gelation on the early-time spreading ($<$ 10ms) of millimetric non-Newtonian drops of biopolymer and particle suspensions impacting a Newtonian liquid containing reactive compounds. Our analyses are initially conducted through experiments by considering a variety of biopolymer and gelling compound concentrations, and impact velocities. The experimental results are then compared to three-dimensional numerical simulations based on a variational multiscale approach, which focuses on the impact of simple viscoplastic drops on a liquid bath in the absence of gelation (non-reactive liquid). These comparisons enable the development of theoretical arguments that emphasise relevant gelation effects on the drop's maximum spreading.

physics.flu-dyn↗

arXiv2018

Microfluidic probing of the complex interfacial rheology of multilayer capsules

Encapsulation of chemicals using polymer membranes enables to control their transport and delivery for applications such as agrochemistry or detergency. To rationalize the design of polymer capsules, it is necessary to understand how the membranes' mechanical properties control the transport and release of the cargo. In this article, we use microfluidics to produce model polymer capsules and study in situ their behavior in controlled elongational flows. Our model capsules are obtained by assembling polymer mono and hydrogen-bonded bilayers at the surface of an oil droplet in water. We also use microfluidics to probe in situ the mechanical properties of the membranes in a controlled elongational flow generated by introducing the capsules through a constriction and then in a larger chamber. The deformation and relaxation of the capsules depend on their composition and especially on the molecular interactions between the polymer chains that form the membranes and the anchoring energy of the first layer. We develop a model and perform numerical simulations to extract the main interfacial properties of the capsules from the measurement of their deformations in the microchannels.

cond-mat.soft↗

arXiv2018

Adsorption dynamics of hydrophobically modified polymers at an air-water interface

Using surface-tension measurements, we study the brush-limited adsorption dynamics of a range of amphiphilic polymers, PAAH-$α$-$\textrm{C}_n$ composed of a poly(acrylic acid) backbone, PAAH, grafted with a fraction $α$ of alkyl moieties, containing either $n=8$ or $n=12$ carbon atoms, at pH conditions where the PAAH backbone is not charged. At short times, the surface tension decreases more sharply as the degree of grafting increases while at long times, the adsorption dynamics becomes logarithmic in time and is slower as the degree of grafting increases. This logarithmic behavior at long times indicates the building of a free-energy barrier which grows over time. To account for the observed surface tension evolution with the degree of grafting we propose a scenario, where the free-energy barrier results from both the deformation of the incoming polymer coils and the deformation of the adsorbed brush. Our model involves only two fitting parameters, the monomer size and the area needed for one molecule during adsorption and is in agreement with the experimental data. We obtain a reasonable value for the monomer size and find an area per adsorbed polymer chain of the order of 1nm$^2$, showing that the polymer chains are strongly stretched as they adsorb.

cond-mat.soft↗

arXiv2018

Five-dimensional imaging of freezing emulsions with solute effects

The interaction of objects with a moving solidification front is a common feature of many industrial and natural processes such as metal processing, the growth of single-crystals, the cryopreservation of cells, or the formation of sea ice. Solidification fronts interact with objects with different outcomes, from the total rejection to their complete engulfment. We image the freezing of emulsions in 5D (space, time, and solute concentration) with confocal microscopy. We show the solute induces long-range interactions that determine the solidification microstructure. The local increase of solute concentration enhances premelting, which controls the engulfment of droplets by the front and the evolution of grain boundaries. Freezing emulsions may be a good analogue of many solidification systems where objects interact with a solidification interface.

cond-mat.mtrl-sci↗

arXiv2018

Transient deformation of a droplet near a microfluidic constriction : a quantitative analysis

We report on experiments that consist in deforming a collection of monodisperse droplets produced by a microfluidic chip through a flow-focusing device. We show that a proper numerical modelling of the flow is necessary to access the stress applied by the latter on the droplet along its trajectory through the chip. This crucial step enables the full integration of the differential equation governing the dynamical deformation, and consequently the robust measurement of the interfacial tension by fitting the experiments with the calculated deformation. Our study thus demonstrates the feasibility of quantitative in-situ rheology in microfluidic flows involving e.g. droplets, capsules or cells.

cond-mat.soft↗

arXiv2017

A temperature-controlled stage for laser scanning confocal microscopy and case studies in chemistry of materials

If confocal microscopy is an ubiquitous tool in life science, its applications in chemistry and materials science are still, in comparison, very limited. Of particular interest in these domains is the use of confocal microscopy to investigate temperature-dependent phenomena such as self-assembly, diffusio- or thermophoresis, or crystal growth. Several hurdles must be solved to develop a temperature-controlled stage for laser scanning confocal microscopy, in particular regarding the influence of an elevated temperature gradient close to the microscope objective, which most people try very hard to avoid. Here we report the design of a temperature-controlled stage able to generate stable temperature gradients in both positive and negative temperature range and does not require use of liquid nitrogen. Our setup provides an excellent control of the temperature gradient, which can be coupled with a controlled displacement of the sample, making it useful in particular for a variety of solidification, chemistry, and interfacial problems. We illustrate the benefits of our setup with several case studies of interest in chemistry and materials science: the 3D real-time imaging of ice growth, the segregation of hard particles by growing crystals, the freezing behaviour of single emulsions, the self-shaping of oil droplets upon cooling, and the self-assembly of amphiphile molecules into helical structures. These results show how confocal microscopy coupled with a temperature-controlled stage is a welcome addition to the toolkit of chemists and materials scientists.

cond-mat.soft↗

arXiv2017

Dynamics and ordering of weakly Brownian particles in directional drying

Drying of particle suspensions is an ubiquitous phenomenon with many natural and practical applications. In particular, in unidirectional drying, the evaporation of the solvent induces flows which accumulate particles at the liquid/air interface. The progressive build-up of a dense region of particles can be used, in particular, in the processing of advanced materials and architectures while the development of heterogeneities and defects in such systems is critical to their function. A lot of attention has thus been paid to correlate the flow and particles dynamics to the ordering of particles. However, dynamic observation at the particle scale and its correlation with local particle ordering are still missing. Here we show by measuring the particle velocities with high frame rate laser scanning confocal microscopy that the ordering of weakly Brownian particles during directional drying in a Hele-Shaw cell opened on one side depends on the particle velocity. Under the ambient and experimental conditions presented in the following, the particle velocities accumulate in two branches. A higher degree of ordering is found for the branch of faster particle velocity which we explain by an increase in the pressure drop which drags the particles into a denser packing as the flow velocity increases. This counter-intuitive behaviour is the opposite to what is found with Brownian particles, which can reorganize by Brownian motion into denser packing during drying, as long as the flow velocity is not too high. These results show that different kinetic conditions can be used to obtain dense, defect-free regions of particles after drying. In particular, it suggests that rapid, directional drying could be used to control the crystallinity of particle deposits.

cond-mat.soft↗

arXiv2017

One-Step Fabrication of pH-Responsive Membranes and Microcapsules through Interfacial H-Bond Polymer Complexation

Biocompatible microencapsulation is of widespread interest for the targeted delivery of active species in fields such as pharmaceuticals, cosmetics and agro-chemistry. Capsules obtained by the self-assembly of polymers at interfaces enable the combination of responsiveness to stimuli, biocompatibility and scaled up production. Here, we present a one-step method to produce in situ membranes at oil-water interfaces, based on the hydrogen bond complexation of polymers between H-bond acceptor and donor in the oil and aqueous phases, respectively. This robust process is realized through different methods, to obtain capsules of various sizes, from the micrometer scale using microfluidics or rotor-stator emulsification up to the centimeter scale using drop dripping. The polymer layer exhibits unique self-healing and pH-responsive properties. The membrane is viscoelastic at pH = 3, softens as pH is progressively raised, and eventually dissolves above pH = 6 to release the oil phase. This one-step method of preparation paves the way to the production of large quantities of functional capsules.

cond-mat.soft↗

arXiv2008

Probing thermal waves on the free surface of various media: Surface Fluctuation Specular Reflection Spectroscopy

Thermal motion gives rise to fluctuations in free surfaces; the propagation of the thermally excited waves on such surfaces depends on the mechanical properties of the medium. Their measurement can therefore provide information on those properties. We have developed an optical tool to probe the thermally excited waves on free surfaces: Surface Fluctuation Specular Reflection (SFSR) spectroscopy. It consists in measuring the fluctuations in the position of a laser beam, which is specularly reflected onto the free surface of a medium, and is therefore sensitive to the roughness of that surface. We show how the measured signal is related to the medium properties. We also present measurements performed on Newtonian liquids as well as on a viscoelastic solid; we show that, in all cases, there is a very good agreement between experimental and computed spectra. SFSR thus applies to a broad range of materials. It moreover offers a very good temporal resolution and should provide a useful tool for dynamical measurements on complex fluids.

cond-mat.soft↗