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Emulsion Stabilization Using Polyelectrolytes

Polyelectrolytes are charged polymers capable of stabilizing (or destabilizing) colloidal emulsions through electrostatic interactions. Their effectiveness can be dependent on molecular weight, pH, solvent polarity, ionic strength, and the hydrophilic-lipohilic balance (HLB). Stabilized emulsions are useful in many industrial processes, including deflocculation, drug delivery, petroleum waste treatment, and food technology.

Types of Polyelectrolytes

Polyelectrolytes are made up of positively or negatively charged repeat units. The charge on a polyelectrolyte depends on the different properties of the solution, such as the degree of dissociation of the monomer units, the solvent properties, salt concentration, pH, and temperature.

Polymers become charged through the dissociation of the monomer side groups (6). If more monomer side groups are dissociated, the polymer has a higher charge. In turn, the charge of the polymer classifies the polyelectrolyte, which can be positive (cationic) or negative (anionic).

The polymer charge and ionic strength of the polyelectrolyte in question dictate how thick a polyelectrolyte layer will be. The thickness of a polyelectrolyte then affects its adsorption ability.

Some examples of polyelectrolytes can be found in the table below. The properties of the polymers vary with molecular weight and degree of polymerization.

Polyelectrolyte and Category	Pka of Monomer Unit (in water)	Molar Mass (g/mol)	Degree of polymerization	Image
PSS (anionic)	-0.53	70,000	340	PSS
PAA (anionic)	4.35	10,000	140	File:PAA.png PAA
APMA (cationic)	5.0	131,000	1528	APMA
PEA (cationic)	7.9	3600	36	File:PEA.png PEA
Poly-L-arginine (cationic)	8.99	15,000-70,000	96-450	Poly-L-arginine

Types of Emulsions

The two main types of emulsions are oil-in-water (nonpolar in polar) and water-in-oil (polar in nonpolar). The difference depends upon the nature of the surfactant or polyelectrolyte in question. If the polyelectrolyte is hydrophilic, it will attract the polar solvent, creating a water-in-oil emulsion. If the polyelectrolyte is hydrophobic, it will attract the nonpolar solvent and create an oil-in-water emulsion.

Emulsion Stability

Schematic representation of flocculation mechanism in SDS-stabilized (top) and surfactant-free (bottom) emulsions.

When there is less interfacial tension between the polyelectrolyte particles and the emulsions in question, emulsions are less stable. This is because the polyelectrolyte particles penetrate the flocs in suspension less when there is less interfacial tension. Thus, cationic polyelectrolytes tend to have decreased penetration and emulsion stability.

Polyelectrolytes may or may not lower the interfacial tension; regardless, they adsorb to the interface the emulsion, and help stabilize it. This means that the oil or water droplets will not coalesce.

On their own, hydrophobic surfactants cannot stabilize an emulsion. Although they are attracted to oil and an “oil in water” emulsion forms, the emulsion will not stay stable for long and will eventually coalesce. With the addition of a polyelectrolyte, electrostatic forces between the oil and water interface are formed and the surfactant begins to act as an “anchor” for the polyelectrolyte, stabilizing the emulsion. In addition to surfactants, nanoparticles can also help stabilize the emulsion by also providing a charged interface for the polyelectrolyte to adsorb on.

Molecular Weight Effects

The stability of the emulsion can depend on the molecular weight of the accompanying polyelectrolyte. Ideally, polyelectrolytes of a high molecular weight are the most effective at stabilization. This is because they form a substantial steric barrier between oil and water, inhibiting aggregation; however, if the polyelectrolyte is too heavy it will not dissolve in the solution. Instead it will form gel lumps and fail to stabilize the emulsion.

pH Effects

The effect of pH on the stability of polyelectrolytes is based upon the functional group on the polymer backbone that is bearing the charge. A protonated amine, for instance, will be much more stable at a lower pH while a sulfonate group will be more stable at a higher pH.

Polymer particles consisting of ionic copolymers result in emulsion stability at either high or low pH, whereas those consisting of nonionic copolymers are generally good emulsifiers at high and low pH values.

Solvent Effects

Polyelectrolytes will be much more soluble in polar solvents due to the charge on the polymer backbone and will spread out more. In nonpolar solvents, polyelectrolytes will coil becoming more densely packed and, if the backbone is nonpolar, will put the charge on the inside of the packed structure.

Ionic Strength

Effects of Salt Condition on Polyelectrolytes

Ionic strength plays a crucial role in emulsion stability. In water-in-oil emulsions as well as many others, the dielectric constant of the solvent is so low that the electrostatic forces between particles do not strong enough to have an effect on emulsion stability. Thus, emulsion stability depends greatly on the polyelectrolyte film thickness.

The polyelectrolyte film thickness is dependent upon its ionic strength. The charged species on polyelectrolyte chains repel each other, causing the chains to stretch out. As the salt concentration increases, ionic strength increases, and the ions will essentially shield the charges on the polymer chain allowing the polymer chain to form a dense random coil.

The effects of ionic strength on a polyelectrolyte in question are based on the charge density of the polymer, however. If the charge density is less than 50% the ionic strength has no effect. As a result the polyelectrolyte film will not increase in thickness.

Hydrophilic-Lipophilic Balance

The Hydrophilic-lipophilic balance (HLB) is measured by the relative amounts of hydrophilic and lipophilic regions on a polymer. The value of the HLB affects the type of emulsions that the polyelectrolyte will stabilize (or destabilize)

Theory

Electrostatic Stabilization

Electrostatic repulsive forces dominate in polyelectrolyte stabilized emulsions. Although there are steric interactions, they are negligible in comparison. As the concentration of polyelectrolyte increases, repulsive forces increase. When there are polyelectrolyte molecules, the distance between individual particles decreases. As the distance h decreases, the exponential term becomes greater. Consequently, the repulsion energy also increases.

This graph illustrates eq. 1. It can be seen that as the surface to surface particle distance decreases, the electrostatic repulsive force decreases exponentially.

The general equation for repulsion energy assuming spherical particles (eq. 1):

$V={\frac {64\pi RCk_{b}T\Gamma e^{-Kh}}{K^{2}}},$

where

R = particle radius

C = bulk concentration of ions

k_b = Boltzmann constant

Γ relates the equation to thermal energy

h is the surface to surface distance of the spherical particles

K is the Debye length

In addition, pH and ionic strength have a great influence on electrostatic interactions because these affect the "magnitude of electrical charge" in solution. As can be seen from the above equation, the repulsion energy depends on the square of the debye length. From the equation for the debye length, it is demonstrated how ionic strength can ultimately affect the electrostatic interactions in a solution.

Bjerrum length

Naturally, the question of the distance at which these electrostatic interactions become important arises. This can be discussed using the Bjerrum length. The Bjerrum length is the distance at which the electrostatic interaction between two charges is comparable to the thermal energy, $k_{B}T$. The distance is given by eq. 2:

$\lambda _{B}={\frac {e^{2}}{4\pi \varepsilon _{r}\varepsilon _{0}\ k_{B}T}},$

where

$e$ = elementary charge

$\varepsilon _{0}$ = vacuum permittivity

$\varepsilon _{r}$ = relative dielectric constant

Surface Charge Density

The surface charge density of these charged surfaces, at low surface potentials, can be modeled using a simplified version of the Grahame equation.

$\sigma ={\varepsilon _{r}\varepsilon _{0}\phi _{0}}{K},$

where

$\phi _{0}$ = surface potential

Polymer	Surface Charge Density $({\frac {C}{m^{2}}})$	Structure
Latex	-0.06	Latex
Pectin	-0.011	Pectin
PAA (0.1% dwb in ZrO2)	-0.088	File:PAA.png PAA

Applications

Deflocculation

When repulsion forces between particles overcome the solution and the loose flocculated aggregates separate, deflocculation occurs. As opposed to the loose and easily separated sediments formed in flocculation, sediments formed in deflocculation are tightly packed and difficult to redisperse.

Depending on the situation, polyelectrolytes can function as either flocculants or deflocculants. In order to stabilize emulsion, deflocculant polyelectrolytes are required. When repulsion forces between particles overcome the solution and the loose flocculated aggregates separate, deflocculation occurs. As opposed to the loose and easily separated sediments formed in flocculation, sediments formed in deflocculation are tightly packed and difficult to redisperse. The repelling forces in a deflocculation increase the zeta potential, which in turn reduces the viscosity of the suspension. Because of this reduction in viscosity, deflocculants are sometimes referred to as “thinning agents”. These thinning agents are usually alkaline and raise the pH of the suspension, preventing flocculation. Deflocculants are used as thinning agents in molding plastics, making glassware, and creating clay ceramics.

Vaccines

Oil in water emulsions are currently used as solvents for vaccines. Polyelectrolyte stabilized emulsions could be used to increase the shelflife of vaccines.

Oil in water emulsions are currently used as safe solvents for vaccines. It is important that these emulsion are stable and remain so for long periods of time. Polyelectrolyte stabilized emulsions could be used to increase the shelf life of vaccines. Researchers have been able to develop polyelectrolyte emulsions with more than six month stability. (2) In addition to being stable for extended periods of time, polyelectrolytes may be useful for vaccines because they can be biodegradable. According to Bio Drug Delivery, the ester bonds of the polyelectrolyte poly(HPMA-DMAE) can undergo hydrolysis in the human body. (3)

Petroleum Waste Treatment

Polyelectrolytes can also act as flocculants, separating solids (flakes) and liquids in industrial processes such as solubilization and oil recovery and they usually have a large cationic charge density.

Using organic materials to refine petroleum instead of iron or aluminum coagulated would greatly decrease that amount of inorganic waste produced. The waste consists of stable oil-in-water emulsions. The addition of various polyelectrolytes to petroleum waste can cause the oil to coagulate, which will make it easier to remove and dispose of, and does not significantly decrease the stability of the solution.

Using organic materials to refine petroleum instead of iron or aluminum coagulated would greatly decrease that amount of inorganic waste produced. The waste consists of stable oil-in-water emulsions. The addition of various polyelectrolytes to petroleum waste can cause the oil to coagulate, which will make it easier to remove and dispose of, and does not significantly decrease the stability of the solution.

Drug Delivery

Hydrolysis of an ester on poly(HPMA-DMAE)

Polyelectrolyte stabilized emulsions are important in the field of nanomedicine. In order to function properly, any drug delivery system must be biocompatible and biodegradable. Polyelectrolytes such as dextran sulfate (DXS), protamine (PRM) or poly-L-arginine all fulfill these requirements and may be used as a capsule with an emulsion inside. There has been research in using this drug delivery method to target leukemia cells.

Polyelectrolyte stabilized emulsions are important in the field of nanomedicine. In order to function properly, any drug delivery system must be biocompatible and biodegradable. Polyelectrolytes such as poly(HPMA-DMAE), dextran sulfate (DSS) or poly-L-arginine all fulfill these requirements and may be used as a capsule with an emulsion inside. Poly(HPMA-DMAE) undergoes ester hydrolysis in the body, and VERO cells envelope DSS and poly-L-arginine to break them down. (Reference Soft Matter drug delivery) Once the polylelectroyte capsule has been degraded, the emulsion containing drug is released into the body. Researchers have been investigating this drug delivery method to target leukemia cells.

Because polyelectrolytes may be biocompatible, it follows that they can be used to stabilize emulsion in foods. Dextran sulfate (DSS), for instance, has been successfully used to induce mixing of proteins and polysaccharides in aqueous emulsions. (5)

Food Technology

Because polyelectrolytes may be biocompatible, it follows that they can be used to stabilize emulsion in foods. Several studies have focused on using polyelectrolytes to inducing mixing of proteins and polysaccarides in oil-in-water emulsions. Dextran sulfate (DSS), for instance, has been successfully used to stabilize these types of emulsions. (5) Other studies have focused on stabilizing oil-in-water emsulsions using β-lactoglobulin (β-Lg), a globular protein, and pectin, an anionic polysaccharide. Both β-lactoglobulin and pectin are common ingredients in the food industry. β-lactoglobulin is used in whey protein, which can act as an emulsifier.