Double W/O/W emulsions consist in an inverse emulsion which is dispersed within a water continuous phase as direct emulsion droplets. The aim of this paper is to explore the basic rules that govern the stability of double emulsions. By associating both water-and oil-soluble surfactants in various concentrations, we produce W/O/W double emulsions. We identify two types of instabilities that are responsible for the evolution of double emulsions: (i) coalescence of the small inner droplets with the globule interface or (ii) coalescence between the small inner droplets within the oil globule. The first type of instability leads to a complete delivering of the small inner droplets toward the external phase whereas the second one does not. We show that the kinetics associated with the release of the small inner droplets due to this former instability is clearly related to the hydrophilic surfactant concentration in the external phase. Depending on the value of this concentration, multiple emulsions may be destabilized with a time scale ranging from several months to a few minutes. We discuss the basic criteria which are responsible for the suppression or the starting of these instabilities, emphasizing the influence of the composition of the interfacial films.

The number of water molecules bound to the dimyristoylphosphatidylcholine (DMPC) interface was investigated both in the fluid (L(alpha)) and gel (L(beta')) phases by solid state deuterium NMR of D2O. We determined that each DMPC molecule binds 9.7 +/- 0.5 and less than 4.3 +/- 0.5 D2O in the fluid and gel phases respectively. These results are accounted for by considering the number of DMPC binding sites as well as the molecular organization in each phase.

We present experimental evidence for viscous sintering phenomena in a gel formed by highly viscous emulsion droplets. When a rupturing agent is added to the initially stable emulsion, a gel forms, which further contracts by preserving the geometry of the container. The initial stages of densification (up to 60%) follow very well the "cylindrical model" for viscous sintering, but deviate at the final stages of densification. The observed inverse dependence of the contraction rate on viscosity is consistent with the viscous sintering theory.

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