Self-Depletion Flocculation of Tetralin Oil-in-Water Emulsions
Alex M. Djerdjev, Robert J. Hunter, and James K. Beattie*
School of Chemistry, UniVersity of Sydney, NSW 2006, Australia
ReceiVed July 6, 2005. In Final Form: September 19, 2005
Oil-in-water emulsions of slightly soluble oils such as tetralin prepared by high-pressure homogenization and
stabilized by sodium dodecyl sulfate undergo depletion flocculation induced by an initially polydisperse droplet size
distribution. The smaller droplets flocculate the larger ones; the flocculation can be reversed by gentle sonication.
After aging, the flocs disappear because the smaller droplets dissolve through Ostwald ripening. These effects were
observed by electroacoustic measurements, supplemented by light scattering.
Introduction
Emulsions are thermodynamically unstable. The droplets can
grow by coalescence or by Ostwald ripening of a polydisperse
population through the slight solubility of the dispersed phase
in the continuous medium. The spatial distribution of an emulsion
can alter by creaming, sedimentation, or flocculation. The latter
can be effected by a bridging agent, such as a polymer, or by
a depletion mechanism due to nonadsorbing polymers, particles,
or micelles.
1
Depletion flocculation is an entropic effect that occurs because
the center of mass of the depleting agent cannot approach the
emulsion droplet more closely than its effective radius. Hence,
there is a shell of volume around the droplet that is not accessible
to the depleting agent, reducing its entropy. If the total depletion
volume of the droplets is reduced by the overlap of their depletion
zones, the excluded volume is decreased, and the volume
accessible to the depleting agent is increased, increasing its
entropy. Hence, there appears to be an attractive force between
the droplets, leading to their flocculation and, ultimately, to phase
separation. The force holding the floc together is weak, however,
and the system can be readily redispersed.
Depletion flocculation of oil-in-water emulsions has been
effected by SDS-micelles,
2,3
nonionic micelles,
4-8
biopolymers
such as hydroxyethyl cellulose,
9,10
xanthan,
11
and proteins.
12-16
None of these depletion agents is present in the system under
study here, yet we still observe what we believe to be depletion
flocculation. In this case, it is caused by the smaller droplets of
the polydisperse population flocculating the larger ones, until
the smaller ones disappear by Ostwald ripening, leading to
spontaneous redispersion of the floc.
In this study, tetralin was chosen as a suitable oil for its relatively
high solubility in water (40 ppm), making Ostwald ripening fast;
its relatively high density (0.966), close to that of water, preventing
significant creaming; and its high boiling point (208 °C),
preventing significant evaporation. The effects described appear
to be general, however, for oils of moderate solubility in water;
we have observed similar behavior with emulsions of hexane
(10 ppm), toluene (515 ppm), and p-cymene (isopropyltoluene)
(350 ppm). In contrast, oils of low solubility in water (<0.1
ppm) such as decane and hexadecane do not show this
phenomenon.
Materials and Method
Chemicals. Tetralin was from BDH Ltd. (>95%), sodium dodecyl
sulfate (SDS) from Sigma (∼99% GC), AR-grade NaCl from Ajax
Chemicals (99%), and ultrapure Milli-Q water from a Millipore
system.
Emulsion Preparation and Measurement. Emulsions were
prepared at a concentration of 5 vol % in aqueous solutions of SDS/
NaCl (5.0 mM/1.0 mM). The oil was emulsified at 25 °C by passing
the mixture through a homogenizer (Milko-tester Mark III F3140,
A/S N. Foss Electric, Denmark) 15 times in rapid succession.
ESA Measurements. Electroacoustic measurements were per-
formed on the emulsion immediately after preparation by injecting
the sample via a syringe into the ESA cell of a prototype of the
AcoustoSizer-II (Colloidal Dynamics Inc., Warwick, RI). The
dynamic mobility of the emulsions was measured at 25 °C and was
observed as a function of time over the course of several hours.
To examine the reversibility of the flocs, the flocculated emulsion
was removed from the cell and sonicated (Unisonics Pty Ltd.,
Australia, 50 Hz) for 30 s and then returned to the cell and remeasured.
After about 3 h, when there was little further change in the ESA
signal, the sample was removed and stored for 1 day. The sample
was then remeasured to observe any changes in the ESA signal.
In another experiment, a tetralin emulsion was prepared and
immediately diluted with SDS/NaCl, (5/1 mM) to 2 or 1 vol % and
measured as a function of time.
Dynamic Light Scattering. The droplet size distribution of a 5
vol % tetralin emulsion was measured by light backscattering with
a Malvern High Performance Particle Sizer immediately after
preparation and then as a function of time.
Results
When a 5 vol % tetralin emulsion was prepared in 5 mM SDS
and 1 mM NaCl and injected into the AcoustoSizer cell, the
dynamic mobility spectra showed dramatic changes over the
* Corresponding author. E-mail: j.beattie@chem.usyd.edu.au.
(1) McClements, D. J. Food Emulsions; CRC Press: Boca Raton, FL, 1999.
(2) Bibette, J. J. Colloid Interface Sci. 1991, 147, 474.
(3) Bibette, J.; Roux, D.; Nallet, F. Phys. ReV. Lett. 1990, 65, 2470.
(4) Fairhurst, D.; Aronson, M. P.; Gum, M. L.; Goddard, E. D. Colloids Surf.
1983, 7, 153.
(5) Aronson, M. P. Langmuir 1989, 5, 494.
(6) Aronson, M. P. Colloids Surf. 1991, 58, 195.
(7) McClements, D. J. Colloids Surf. A 1994, 90, 25.
(8) Shields, M.; Ellis, R.; Saunders, B. R. Colloids Surf. A 2001, 178, 265.
(9) Manoj, P.; Fillery-Travis, A. J.; Watson, A. D.; Hibberd, D. J.; Robins,
M. M. J. Colloid Interface Sci. 1998, 207, 283.
(10) Manoj, P.; Watson, A. D.; Hibberd, D. J.; Fillery-Travis, A. J.; Robins,
M. M. J. Colloid Interface Sci. 1998, 207, 294.
(11) Chanamai, R.; Herrmann, N.; McClements, D. J. J. Colloid Interface Sci.
1998, 204, 268.
(12) Hemar, Y.; Pinder, D. N.; Hunter, R. J.; Singh, H.; He ´braud, P.; Horne,
D. S. J. Colloid Interface Sci. 2003, 264, 502.
(13) Dickinson, E.; Radford, S. J.; Golding, M. Food Hydrocolloids 2003, 17,
211.
(14) Berli, C. L. A.; Quemada, D.; Parker, A. Colloids Surf. A 2002, 203, 11.
(15) Radford, S. J.; Dickinson, E. Colloids Surf. A 2004, 238, 71.
(16) Blijdenstein, T. B. J.; Veerman, C.; van der Linden, E. Langmuir 2004,
20, 4881.
84 Langmuir 2006, 22, 84-87
10.1021/la0518041 CCC: $33.50 © 2006 American Chemical Society
Published on Web 11/23/2005