Small-angle neutron scattering was used to probe the interfacial structure of nitrogen-in-water foams created using a series of tri-block polymeric surfactants of the poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (EOx-POy-EOx) range, from which the nature of the polymeric interface could be characterised. The data follow a pronounced Q-4 decay, along with a number of inflexions and weak but well-defined peaks. These characteristics were well-described by a model embodying paracrystalline stacks of adsorbed polymer layers, whose formation is induced by the presence of the air-water interface, adsorbed at the flat air-water (film lamellae) interface. A minimum of approximately five paracrystalline polymer layers of thickness of the order of 85-160 Å, interspersed with somewhat thicker (400 Å) films of continuous aqueous phase were found to best fit the data. The thickness of the layer (L) was shown to follow a relationship predicted by anchor block dominated polymer adsorption theories from non-selective solvents, L ∼ EO1PO1/3. The insight gained from these studies should permit a more rational design of polymeric stabilisers for hydrophilic polyurethane foams. This journal is © the Partner Organisations 2014.
CITATION STYLE
Hurcom, J., Paul, A., Heenan, R. K., Davies, A., Woodman, N., Schweins, R., & Griffiths, P. C. (2014). The interfacial structure of polymeric surfactant stabilised air-in-water foams. Soft Matter, 10(17), 3003–3008. https://doi.org/10.1039/c3sm52877d
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