Publications by authors named "J Giermanska-Kahn"

We kinetically stabilize oil-in-water emulsions comprising paraffin crystals by adsorbing solid particles (silica) of colloidal size at the oil/water interface. We obtain a set of emulsions that are quiescently stable for a long period of time (months), while the same emulsions are destabilized after only a few hours in the presence of surfactant molecules alone. The emulsions are submitted to a shear stress in order to probe their stability under flow conditions.

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Solid-stabilized emulsions are obtained by shearing a mixture of oil, water, and solid colloidal particles. In this article, we present a large variety of materials, resulting from a limited coalescence process. Direct (o/w), inverse (w/o), and multiple (w/o/w) emulsions that are surfactant-free and monodisperse were produced in a very wide droplet size range, from micrometers to centimeters.

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The viscoelastic properties of insoluble monolayers have been investigated by the excited electrocapillary waves method. Effective negative values of dilational viscosities have been obtained in the liquid expanded and liquid condensed phases of insoluble monolayers of myristic, pentadecanoic, and stearic acids. However, the surface viscosity remains positive for the more expanded monolayers of ethyl palmitate ester.

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Water-in-oil-in-water double emulsions (W/O/W) consist of dispersed oil globules containing smaller aqueous droplets. These materials offer interesting possibilities for the controlled release of chemical species initially entrapped in the internal droplets. A better understanding of the stability conditions and release properties in double emulsions requires the use of model systems with a well-defined droplet size.

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We study the kinetics of the release of monodisperse water-in-oil-in-water double emulsions in the regime dominated by coalescence of the internal aqueous droplets onto the globule interface. By measuring the rate of release of adsorbed droplets, we directly determine the average lifetime of the thin film that forms between the small internal droplets and the globule surface. Therefore, the activation energy and the natural frequency of the hole nucleation process within the adhesive thin liquid films are unambiguously deduced.

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