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.

Growth Mechanism of Polymer Membranes Obtained by H-Bonding Across Immiscible Liquid Interfaces.

Complexation of polymers at liquid interfaces is an emerging technique to produce all-liquid printable and self-healing devices and membranes. It is crucial to control the assembly process, but the mechanisms at play remain unclear. Using two different reflectometric methods, we investigate the spontaneous growth of H-bonded PPO-PMAA (polypropylene oxide-polymetacrylic acid) membranes at a flat liquid-liquid interface.

Microfluidic probing of the complex interfacial rheology of multilayer capsules.

Encapsulation of chemicals using polymer membranes enables control of 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 divergent flows.

Experimental and numerical study of platelets rolling on a von Willebrand factor-coated surface.

Blood platelets circulate in the blood and adhere to wounded vessels to initiate coagulation and healing. The first step of this process is the capture of flowing platelets by adhesive molecules located at the wounded vessel wall. In this article, we study the transport of fixed blood platelets in a microfluidic channel coated with von Willebrand factor (vWF), a large multimeric protein expressed by endothelial cells in the vicinity of wounds.

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.

Interfacial Rheology of Hydrogen-Bonded Polymer Multilayers Assembled at Liquid Interfaces: Influence of Anchoring Energy and Hydrophobic Interactions.

We study the 2D rheological properties of hydrogen-bonded polymer multilayers assembled directly at dodecane-water and air-water interfaces using pendant drop/bubble dilation and the double-wall ring method for interfacial shear. We use poly(vinylpyrrolidone) (PVP) as a proton acceptor and a series of polyacrylic acids as proton donors. The PAA series of chains with varying hydrophobicity was fashioned from poly(acrylic acid), (PAA), polymethacrylic acid (PMAA), and a homemade hydrophobically modified polymer.

Microfluidic model of the platelet-generating organ: beyond bone marrow biomimetics.

We present a new, rapid method for producing blood platelets in vitro from cultured megakaryocytes based on a microfluidic device. This device consists in a wide array of VWF-coated micropillars. Such pillars act as anchors on megakaryocytes, allowing them to remain trapped in the device and subjected to hydrodynamic shear.

Dynamical superhydrophobicity.

Superhydrophobicity is mainly remarkable for the special dynamical behaviours it generates: low adhesion, giant hydrodynamic slip, frictionless motion, rebounds after impacts. Here we discuss most of these properties. We first recall how contact angle hysteresis can be minimized in this state.

Contact angle hysteresis generated by strong dilute defects.

Water on solid decorated with hydrophobic defects (such as micropillars) often stays at the top of the defects in a so-called fakir state, which explains the superhydrophobicity observed in such case, provided that the density of defects is small enough. Here we show that this situation provides an ideal frame for studying the contact angle hysteresis; the phase below the liquid is "perfect" and slippery (it is air), contrasting with pillars' tops whose edges form strong pining sites for the contact line. This model system thus allows us to study the hysteresis as a function of the density of defects and to compare it to the classical theory by Joanny and de Gennes, which is based on very similar hypothesis.

Non-adhesive lotus and other hydrophobic materials.

Superhydrophobic materials recently attracted a lot of attention, owing to the potential practical applications of such surfaces--they literally repel water, which hardly sticks to them, bounces off after an impact and slips on them. In this short review, we describe how water repellency arises from the presence of hydrophobic microstructures at the solid surface. A drop deposited on such a substrate can float above the textures, mimicking at room temperature what happens on very hot plates; then, a vapour layer comes between the solid and the volatile liquid, as described long ago by Leidenfrost.