Foaming of Transient Polymer Hydrogels.

Foams made with polymer hydrogels can be used in a variety of applications, such as scaffolds for biomedical applications or decontamination processes. However, from a practical point of view, it is difficult to introduce bubbles into viscous or viscoelastic fluids and to produce large volumes of hydrogel foams. In the present article, we investigate the foaming process of poly(vinyl alcohol) (PVA)/borax transient hydrogels, where PVA chains reversibly bind to borax molecules. In a previous article, we showed that foams obtained with PVA/borax mixtures are highly stable because of both high interfacial and bulk viscosities and can be used to quickly absorb liquids, which make them suitable for detergency or decontamination processes. To produce these foams, we use a two-step foaming process which consists in first shearing a PVA solution to obtain a PVA foam and second adding borax to the PVA foam under continuous shearing. The obtained PVA/borax foams are stable for weeks. In this study, we observe a shear-induced collapse of the foams for formulations containing a low borax/PVA ratio, whereas they remain stable under shear for high PVA/borax ratios. Using scaling arguments, we find that the shear-induced collapse of the foams and bubbles is obtained below a critical ratio, N E/N B = 15, of the number of entanglements per chain, N E, and the number of borax per chain, N B. Rheology measurements show that the samples present a shear-thickening behavior that increases with the borax concentration. We suggest that during the foaming process when the shearing rate is of the order of 100 s-1, the viscosity of these samples diverges, leading to a viscous to fragile transition. To mimic the fast stretching of the PVA/borax thin films during the foaming process, we study the stretching of individual PVA/borax catenoid-shaped thin films at high stretching rates. We observe that the films containing low PVA/borax ratios do not minimize their surface area unlike what is theoretically expected for standard surfactant films. Moreover, the films tend to be unstable and fracture because the PVA/borax network does not have time to rearrange and relax stresses for high stretching rates.

Time scales for drainage and imbibition in gellified foams: application to decontamination processes.

We probe the drainage and imbibition dynamics of foams in which the continuous aqueous phase is a transient gel-like network. To produce these foams, we provide a new method - a PVA (polyvinyl alcohol) solution is first foamed and then a cross-linker, Borax, is added, which binds reversibly to the PVA chains. The resulting foams are ultra-stable-over a month. We find that the typical time for gravitational drainage of the continuous phase can be slowed down from hours to several weeks by tuning the Borax concentration. We show that the Borax concentration controls both the bulk viscosity of the continuous phase and the surface viscosity of the air-water interfaces. From these results we suggest that the PVA molecules adsorbed at the bubble interfaces are highly cross-linked by the Borax molecules. We find that the capillary rise of a dyed liquid into these foams is orders of magnitude faster than the drainage flow, meaning that these foams can quickly absorb liquids. These results show that these foams could be used to clean or decontaminate surfaces covered with liquid wastes. Indeed we show that the PVA-Borax foam can easily be spread on a surface, absorb a liquid without destabilizing and be dried afterward to recover the waste.

Mixtures of latex particles and the surfactant of opposite charge used as interface stabilizers--influence of particle contact angle, zeta potential, flocculation and shear energy.

We investigate the stabilization of air-water interfaces by mixtures of negatively charged latex particles (sulfate polystyrene) and cationic surfactants (alkyl trimethylammonium bromides). First we report results concerning the binding of surfactant molecules to the latex particles. As the surfactant concentration increases, the charge of the particles reverses, from negative to positive, because CnTAB first binds electrostatically to the latex particles and then through hydrophobic interaction with the monolayer already adsorbed on the particles as well as directly with the hydrophobic surface of the latex. Over a large range of surfactant concentrations around the charge inversion, a strong flocculation is observed and 100 µm large aggregates form in the suspension. Unlike previous studies published on mixtures of inorganic particles with oppositely charged surfactants, we show that we can vary the sign of the zeta potential of the particles without changing the contact angle of the particles over a large range of surfactant concentrations. Indeed, the latex particles that we study are more hydrophobic than inorganic particles, hence adding moderate concentrations of the surfactant results in a weak variation of the contact angle while the charge of the particles can be reversed. This enables decoupling of the effect of zeta potential and contact angle on the interfacial properties of the mixtures. Our study shows that the contact angle and the charge of the particles are not sufficient parameters to control the foam properties, and the key-parameters are the flocculation state and the shear energy applied to produce the foam. Indeed, flocculated samples, whatever the sign of the zeta potential, enable production of a stable armour at the interface. The large aggregates do not adsorb spontaneously at the interface because of their large size, however when a large shear energy is used to produce the foam very stable foam is obtained, where particles are trapped at interfaces. We suggest that the large aggregates may be broken during shear and may reform at the interface to form a solid armour. A simple calculation taking into account the adsorption dynamics of the aggregates as a function of their size is consistent with this hypothesis.