Novel stabilisation of emulsions by soft particles: polyelectrolyte complexes

被引:25
作者
Rodriguez, Ana Maria Bago [1 ]
Binks, Bernard P. [1 ]
Sekine, Tomoko [2 ]
机构
[1] Univ Hull, Dept Chem, Kingston Upon Hull HU6 7RX, N Humberside, England
[2] Shiseido Global Innovat Ctr, Tsuzuki Ku, 2-2-1 Hayabuchi, Yokohama, Kanagawa 2248558, Japan
关键词
IN-WATER EMULSIONS; HIGHLY AGGREGATING SYSTEMS; INTERFACIAL-TENSION; PICKERING EMULSIONS; SODIUM CASEINATE; MOLECULAR-WEIGHT; SOLID PARTICLES; EMULSIFYING PROPERTIES; SOY PROTEIN; STABILITY;
D O I
10.1039/c6fd00011h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We put forward the concept of a novel particle stabiliser of oil-water emulsions, being the polyelectrolyte complex (PEC) formed between oppositely charged water-soluble polymers in cases where either polymer alone is incapable of stabilising an emulsion. Using poly(4-styrene sulfonate) sodium salt, PSSNa and poly(diallyldimethylammonium chloride), PDADMAC, of low polydispersity and similar molecular mass, we correlate the behaviour of their mixtures in water with that of emulsions after addition of oil. In aqueous mixtures, spherical particles of diameters between 100 and 150 nm are formed through electrostatic interactions between charged polymer chains. Around equal mole fractions of the two polymers, the zeta potential of the particles reverses in sign and emulsions of oil-in-water (o/w) for a range of oils can be prepared which are the most stable to coalescence and creaming. The effects of PEC concentration and the oil : water ratio have been examined. All emulsions are o/w and stability is achieved by close-packed particle layers at drop interfaces and particle aggregation in the continuous phase. Increasing the salt concentration initially causes destabilisation of the aqueous particle dispersion due to particle aggregation followed by dissolution of particles at high concentrations; the corresponding emulsions change from being stable to completely unstable and are then re-stabilised due to adsorption of uncharged individual polymer molecules.
引用
收藏
页码:255 / 285
页数:31
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