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
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.