# Difference between revisions of "Emulsions"

## Introduction

Emulsions are unbiquous ... and some of the most interesting and challenging are in foods:

Dickenson, Food Science.

Microfluidics are terrific ... where can we add the "magic" of emulsion science?

## Terminology

 Macroemulsions Miniemulsions At least one immiscible liquid dispersed in another as drops whose diameters generally exceed 1000 nm. The stability by addition of surfactants and/or finely divided solids. Considered only kinetically stable. An emulsion with droplets between 100 and 1000 nm. Reportedly thermodynamically stable. A thermodynamically stable, transparent solution of micelles swollen with solubilizate. Usually requires a surfactant and a cosurfactant (e.g. short chain alcohol).

Becher, P. Emulsions, theory and practice, 3rd ed.; Oxford University Press: New York; 2001.

## Emulsion processes

Dickenson?
 A - Inversion C - Sedimentation E - Coalescence B - Creaming D - Flocculation F - Ripening

The stability of emulsions is determined by a variety of factors:

 Electrostatic stabilization at lower volume fractions Steric stabilization at all volume fractions Additional factors Temperature is important – solubility changes quickly. Steric stabilization is enhanced by solubility in both phases: Mixed emulsifiers (cosurfactants) are common. They can come from either phase.

The creaming of emulsion can be shown by the variation in volume fraction at various heights and times as determined by measuring the speed of sound:

Morrison, Fig. 22.13

Emulsion inversion - As the concentration increases (A) the droplets get closer until they pinch off into smaller, opposite type of emulsion (B).

## Making emulsions

Method of phase inversion e.g. Use a poor O/W emulsifier, go to high volume fractions, the emulsion inverts to smaller droplets of W/O
Phase-inversion-temperature method e.g. Heat and emulsify O/W 2-4o below the PIT, creates low s and small drops, cool to room temperature.
Solubilize vapor in micelles The energies driving the condensation, drive Ostwald ripening, therefore a formulation challenge.
Electric emulsification Charging the surface produces electrohydrodynamic instabilities.
Intermittent milling Surfactant adsorption is slow – waiting helps.

Intermittent milling

## Breaking emulsions

From: Menon, V.B.; Wasan, D.T. Demulsification, in Encyclopedia of emulsion technology; Becher, P., Ed.; Marcel Dekker: New York; 1985, Vol. 2; pp 1-75.

 Creaming Especially with a centrifuge, taking advantage of temperature and salt. Sometime high shear; filtering through bed whose surfaces are wetted by internal phase; ultrafiltration; dialysis; Most emulsion a less stable hot; At the PIT many are quite unstable; freeze-thaw. Chemically change the emulsifier; mismatch of HLB, pH; replace with strong surfactant but not strong emulsifier; addition of other solvents.

## Bancroft's rule and the HLB

Bancroft's Rule:

The emulsifier stabilizes the emulsion type where the continuous phase is the medium in which it is most soluble.
A hydrophilic solute in an O/W emulsion.
The long tail on the surfactant is to represent the longer range interaction of a hydrophilic molecule through water.
A hydrophilic solute in a W/O emulsion.

The Hydrophile-Lipophile Schema:

Variation of type and amount of residual emulsion with HLB number of emulsifier at room temperature. Morrison, Fig. 22.5

## Phase inversion temperatures

The "type" of an emulsifier often changes with increasing temperature; typically from being water soluble, hence a high HLB number to being water insoluble, hence a low HLB number. Therefore the type (O/W or W/O) emulsion it stabilizes changes. The temperature of the transition is called the Phase Inversion Temperature or PIT.

www.bias-net.com/chimica/pdf/set_baglioni.pdf

The HLB and the PIT are often related:

## Interfacial properties

Morrison, Fig. 22.8

The rheology of O/W interfaces can be examined by measuring the diffusion of traced particles at the interface:

Wu and Dai, Langmuir, 23, 4324 – 4331, 2007.
For viscous liquids: $\left\langle \Delta r^{2}\left( \tau \right) \right\rangle =4D\tau \text{ where }D=\frac{k_{B}T}{4\pi \eta a}\,\!$

For elastic liquids: $\left\langle \Delta r^{2} \right\rangle =\frac{2k_{B}T}{3\pi a{G}'}\,\!$

The particles have to sit properly at the O/W interface.

## Multiple emulsions

Rosen, p. 313
 (a) W/O/W double emulsion (b) O/W/O double emulsion Consider, for either diagram: Each interface needs a different HLB value. The curvature of each interface is different.

## Particles as emulsion stabilizers

Almost all particles are only partially wetted by either phase. When particles are “adsorbed” at the surface, they are hard to remove – the emulsion stability is high, sometimes thousands of kT. Crude oil is a W/O emulsion and is old!! Morrison, Fig. 22.3

Variation of the free energies of desorption (relative to kT) of a spherical particle 10 nm radius at a planar O/W interface of interfacial tension of 36 mN/m with a contact angle which the particle makes with the interface (measured through the oil phase) at 298 K. Morrison, Fig. 22.4

The thermodynamics is rich.
Wu and Dai, Langmuir, 23, 4324 – 4331, 2007.
Wu and Dai, Langmuir, 23, 4324 – 4331, 2007.
Wu and Dai, Langmuir, 23, 4324 – 4331, 2007.
Figure 7. Sketch of a particle of radius a, which is bridging between the surfaces of a film from phase 2 formed between two drops of phase 1. h is the film thickness. $\sigma$ is the contact angle. Figure 8. Definitions of phases, angles, and emulsions: By definition, the particles are initially dispersed in phase 2. The contact angle, $\sigma$, is always measured across phase 2. The emulsion 1-in-2 is a Bancroft-type emulsion, in which the particles are dispersed in the continuous phase. In contrast, the emulsion 2-in-1 is of anti-Bancroft type.

Hydrophilic silica stabilizing a wax/water emulsion:

J. Giermanska-Kahn,† V. Laine,† S. Arditty,† V. Schmitt,† and F. Leal-Calderon
Langmuir 2005, 21, 4316-4323
Figure 1. Microscopic image of a paraffin-in-water emulsion stabilized by CTAB alone. T ) 25 °C. Figure 3. Microscopic image of a paraffin-in-water emulsion stabilized by P2 particles. Inset: same image taken at T ) 25 °C under crossed polarizers, confirming the presence of crystals

in the droplets.

## Texturas by Ferran Adria

In his recent visit to Harvard, world-famous chef and culinary innovator Ferran Adria gave several video demonstrations of his cutting-edge cooking techniques. He spoke of his desire to create a new language of food. Some chef in the past made the first salad, the first soup, and the first bread, and now there are thousands of varieties of each. Each of these examples could be considered new "words" that could create a new world of culinary possibilities. Over the past decades, he has been searching for fundamental advances in cooking that could be considered new letters of the culinary alphabet.

This new alphabet is exemplified by Albert and Ferran Adria's new line of Texturas, various chemicals that enable new culinary experiences. Below are some specific cases related to emulsions:

* Lecite: Soy-based lecithen was discovered at the end of the 19th century and has now made its way into may of Ferran Adria's new creations, especially the airs. This particular form comes as a fine powder that is soluble in water, even at cool temperatures. As the website says, lecite is ideal for "converting juices and other watery materials into airs."

• Sucro: This form of sacarose is already widely used in Japan to create water-in-oil type emulsions. This form also comes in a water-soluble powder, which dissolves even at cool temperatures.
• Glice: The mono- and di-glyceride emulsifier comes in a powdered form. Unlike the other two emulsifiers, it is only soluble in oil heated past 60 C.