arXiv subjects

A. Deblais

Publications and source records attributed to A. Deblais.

6 recordsLinked to original sources

arXiv2025

Collecting Particles in Confined Spaces by Active Filamentous Matter

Biological and robotic systems often operate in confined environments where material must be gathered without centralized control. Inspired by the effective collection strategies of aquatic worms (Lumbriculus variegatus and Tubifex tubifex), we investigate how active filaments autonomously aggregate dispersed particles. We study this process across four platforms: living worms, a robotic chain, Brownian dynamics simulations of active polymers, and a coarse-grained toy model. We show that aggregation emerges from repeated contact and body deformation, and demonstrate that clustering dynamics are governed by filament length and bending stiffness. Across systems, particle gathering follows a shared aggregation-fragmentation process, with the steady-state average cluster size scaling as $\langle s\rangle_L\sim W/D^2$, where W is the effective width of the path cleared by the filament and D the domain size. We find that filament flexibility modulates W, enabling more flexible filaments to sweep larger areas and collect more particles. These results establish a unifying framework for understanding how shape and flexibility influence transport and organization in active filament systems and filamentous robots.

cond-mat.soft↗

arXiv2024

When does the elastic regime begin in viscoelastic pinch-off?

In this experimental and numerical study, we revisit the question of the onset of the elastic regime in viscoelastic pinch-off. This is relevant for all modern filament thinning techniques which aim at measuring the extensional properties of low-viscosity polymer solutions such as the Slow Retraction Method (SRM) in Capillary Breakup Extensional Rheometry (CaBER) as well as the dripping method where a drop detaches from a nozzle. In these techniques, a stable liquid bridge is slowly brought to its stability threshold where capillary-driven thinning starts, slowing down dramatically at a critical radius $h_1$ marking the onset of the elastic regime where the bridge becomes a filament with elasto-capillary thinning dynamics. While a theoretical scaling for this transition radius exists for the classical step-strain CaBER protocol, where polymer chains stretch without relaxing during the fast plate separation, we show that it is not necessarily valid for a slow protocol such as in SRM since polymer chains only start stretching (beyond their equilibrium coiled configuration) when the bridge thinning rate becomes comparable to the inverse of their relaxation time. We derive a universal scaling for $h_1$ valid for both low and high-viscosity polymer solution which is validated by both CaBER (SRM) experiments with different polymer solutions, plate diameters and sample volumes and by numerical simulations using the FENE-P model.

cond-mat.soft↗

arXiv2021

Stringiness of Hyaluronic Acid Emulsions

In this work, we underline the importance of the molecular weight of hyaluronic acid on the elongational properties of concentrated emulsions. The filament formation properties, e.g. the stringiness, of an emulsion is a key determinant of a product liking and repeat purchase. Here, we find that high molecular weight hyaluronic acid and a high stretching speed are the control parameters affecting the filament formation of an emulsion.

cond-mat.soft↗

arXiv2021

Self-similarity in the breakup of very dilute viscoelastic solutions

When pushed out of a syringe, polymer solutions form droplets attached by long and slender cylindrical filaments whose diameter decreases exponentially with time before eventually breaking. In the last stages of this process, a striking feature is the self-similarity of the solution shape near the end of the filament. This means that shapes at different times, if properly rescaled, collapse onto one universal shape. A theoretical description inspired by this similarity observation and based on the Oldroyd-B model was recently shown to disagree with existing experimental results. By revisiting these measurements and analysing the interface profiles of very diluted polyethylene oxide solutions at high temporal and spatial resolution, we show that they are very well described by the model.

cond-mat.soft↗

arXiv2021

Capillary Thinning of Elastic and Viscoelastic Threads: from Elastocapillarity to Phase Separation

The formation and destabilisation of viscoelastic filaments are of importance in many industrial and biological processes. Filament instabilities have been observed for viscoelastic fluids but recently also for soft elastic solids. In this work, we address the central question how to connect the dynamical behavior of viscoelastic liquids to that of soft elastic solids. We take advantage of a biopolymer material whose viscoelastic properties can be tuned over a very large range by its pH, and study the destabilization and ensuing instabilities in uniaxial extensional deformation. In agreement with very recent theory, we find that the interface shapes dictated by the instabilities converge to an identical similarity solution for low-viscosity viscoelastic fluids and highly elastic gels. We thereby bridge the gap between very fluid and strongly elastic materials. In addition, we provide direct evidence that at late times an additional filament instability occurs due to a dynamical phase separation.

cond-mat.soft↗

arXiv2020

Phase Separation by Entanglement of Active Polymerlike Worms

We investigate the aggregation and phase separation of thin, living T. tubifex worms that behave as active polymers. Randomly dispersed active worms spontaneously aggregate to form compact, highly entangled blobs, a process similar to polymer phase separation, and for which we observe power-law growth kinetics. We find that the phase separation of active polymerlike worms does not occur through Ostwald ripening, but through active motion and coalescence of the phase domains. Interestingly, the growth mechanism differs from conventional growth by droplet coalescence: the diffusion constant characterizing the random motion of a worm blob is independent of its size, a phenomenon that can be explained from the fact that the active random motion arises from the worms at the surface of the blob. This leads to a fundamentally different phase-separation mechanism that may be unique to active polymers.

cond-mat.soft↗