Colloid chemical stability and interfacial properties of mixed phospholipid-non-ionic surfactant stabilised oil-in-water emulsions

Citation
D. De Vleeschauwer et P. Van Der Meeren, Colloid chemical stability and interfacial properties of mixed phospholipid-non-ionic surfactant stabilised oil-in-water emulsions, COLL SURF A, 152(1-2), 1999, pp. 59-66
Citations number
26
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
ISSN journal
09277757 → ACNP
Volume
152
Issue
1-2
Year of publication
1999
Pages
59 - 66
Database
ISI
SICI code
0927-7757(19990715)152:1-2<59:CCSAIP>2.0.ZU;2-M
Abstract
Phospholipid-stabilised emulsions are known to have a poor stability when p repared in the presence of electrolytes. In order to try to circumvent this problem, submicron-sized 5% o/w emulsions were prepared in the presence of up to 500 mM KCl or up to 50 mM CaCl2 using either only steric stabilisers or a combination of steric stabilisers and phospholipids. Steric surfactan ts are believed to provide a steric repulsion barrier around the emulsion d roplets, and as such should withstand electrolyte addition better than the mainly electrostatically-stabilised phospholipid emulsions. The emulsion st ability was investigated by measuring the particle size of the emulsion dro plets as a function of time by photon correlation spectroscopy. Emulsions s tabilised only by 0.5% (w/v) of the steric surfactants were completely stab le in the presence of electrolytes. It was also shown that the addition of even low concentrations of the steric surfactants (0.025% to 0.05%) indeed dramatically improved the stability of phospholipid-stabilised emulsions in the presence of electrolytes. I n order to investigate this behaviour more fundamentally the thickness of t he polymer layer adsorbed on the emulsion droplet surface was determined by viscosity and by zeta-potential measurements. Subsequently, these data wer e used in quantitative models based on the DLVO theory for the electrostati c interactions and on the equation of Ottewill and Walker for the steric re pulsion contribution. Keeping account of the experimentally determined adso rbed layer thickness, particle size and surface potential, which was deduce d from the zeta-potential, total interaction energy diagrams of the emulsio ns were drawn. These models allowed us to make theoretical predications abo ut the emulsion stability, and the conclusions regarding emulsion stability agreed with the experimental results. (C) 1999 Elsevier Science B.V. All l ights reserved.