The adsorption kinetics of mixtures of a biosurfactant Quillaja Bark Saponin (QBS) with a globular protein, β-lactoglobulin (β-LG) at the water/air and water/tetradecane interfaces was investigated by measuring dynamic interfacial tension with axisymmetric drop shape analysis (ADSA) and maximum bubble pressure (MBP) techniques. With bulk concentration of β-LG fixed at 10(-7) M, the most pronounced synergistic effects in the rate of the QBS adsorption at both interfaces were observed at low biosurfactant concentrations (5 × 10(-7)-1 × 10(-5) M). The synergistic effect due to a protein-biosurfactant complex formation is clearly noticeable, yet less pronounced than, e.g., previously studied QBS/lysozyme mixtures. The surface pressures attained at water/oil interface are higher than in the water/air system, although, at high biosurfactant/protein ratios, the presence of β-LG decelerates adsorption of the QBS/β-LG complex onto the water/tetradecane interface. In analogy to mixtures of synthetic surfactants with proteins, the adsorbed layer gets dominated by QBS at higher biosurfactant concentrations, although the presence of β-LG affects the surface pressures attained even at QBS/β-LG ratios as high as 10(4). The synergistic effects are much less noticeable in foamability and emulsion formation/stability, as probed by the modified Bikerman's and dynamic light scattering (DLS) techniques, respectively.
A simple and effective way to synthesize hollow silicone resin particles of controlled diameter is presented. The synthesis utilizes catanionic vesicles as templates for the polycondensation/polymerization processes of 1,3,5,7tetramethylcyclotetrasiloxane (D 4 H ) within their membranes. Two different surfactant systems were used to form the vesicular templates: mixtures of dodecyltrimethylammonium bromide (DTAB) and sodium dodecylbenzenesulfonate (SDBS) in the cationic (the DTAB/SDBS system) or anionic (the SDBS/DTAB system) rich region of the phase diagram. The templates obtained from these surfactant mixtures form spontaneously unilamellar vesicles in aqueous solution. The vesicular templates swell upon addition of D 4 H , thus increasing their size. The silicone resin was obtained in acid-or base-catalyzed polycondensation and ring-opening polymerization processes of D 4 H . In the case of the DTAB/SDBS system the formation of a densely cross-linked silicone material with SiO 3/2 units allowed the nanocapsules to retain the vesicular shape after removal of the template, whereas in the SDBS/DTAB system, the polymer produces capsules which are too smooth to support surfactant lysis. The morphology of the silicone nanocapsules was analyzed using transmission electron microscopy (TEM) and, in some cases, atomic force microscopy (AFM). TEM and AFM reveal discrete hollow particles with a small amount of linked or aggregated hollow silica shells.
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