# Thermodynamics of micellization

The surfactant’s critical micelle concentration (CMC) plays a factor in Gibbs free energy of micellization. The exact concentration of the surfactants that yield the aggregates being thermodynamically soluble is the CMC. The Krafft temperature determines the solubility of the surfactants which in turn is the temperature that CMC is achieved. There are many parameters that affect the CMC. The interaction between the hydrophilic heads and the hydrophobic tails play a part, as well as the concentration of salt within the solution and surfactants.

## Micelle

A micelle is an aggregation of surfactants or block copolymer in aqueous solution or organic solution, often spherical.

### Surfactants

Surfactants are composed of a polar head group that is hydrophilic and a nonpolar tail group that is hydrophobic. The head groups can be anionic, cationic, zwitterionic, or nonionic. The tail group can be a hydrocarbon, fluorocarbon, or a siloxane. Extensive variation in the surfactant’s solution and interfacial properties is allowed through different molecular structures of surfactants.[1]

Hydrophobic coagulation occurs when a positively charged solution is added with a sodium alkyl sulfate. The coagulation value is smaller when the alkyl chain length of the coagulator is longer. Hydrophobic coagulation occurs when a negatively charged solution contains a cationic surfactant. The coulomb attraction between the head groups and surface competes with the hydrophobic attraction for the entire tail in a favorable manner.[1]

### Block copolymer

Block copolymers are interesting because they can "microphase separate" to form periodic nanostructures,[13][14][15] Microphase separation is a situation similar to that of oil and water. Oil and water are immiscible - they phase separate. Due to incompatibility between the blocks, block copolymers undergo a similar phase separation. Because the blocks are covalently bonded to each other, they cannot demix macroscopically as water and oil. In "microphase separation" the blocks form nanometer-sized structures.

## Driving mechanism for micellization

The driving mechanism for micellization is the transfer of hydrocarbon chains from water into the oil-like interior. This entropic effect is called the hydrophobic effect. Compared to the increase of entropy of the surrounding water molecules, this hydrophobic interaction is relatively small. The water molecules are highly ordered around the hydrocarbon chain. The CMC decreases while the length of the alkyl chain increases when all the hydrocarbon chains are hidden inside micelles.[2]

## Gibbs free energy of micellization

In general, the Gibbs free energy of micellization can be approximated as:

${\displaystyle \Delta G_{micellization}=RT\times \ln(CMC)}$[1]

where ${\displaystyle \Delta G_{micellization}}$ is the change in Gibbs free energy of micellization, ${\displaystyle R}$ is the universal gas constant, ${\displaystyle T}$ is the absolute temperature, and ${\displaystyle CMC}$ is the critical micelle concentration.

### Non-ionic micelles

Two methods to extract the Gibbs free energy based on the value of CMC and ${\displaystyle n}$ exist; Phillips method[3] based on the law of mass action and the pseudo-phase separation model. The law of mass action postulates that the micelle formation can be modeled as a chemical equilibrium process between the micelles ${\displaystyle M_{n}}$ and its constituents, the surfactant momomers, ${\displaystyle S}$:

${\displaystyle n\cdot S\rightleftharpoons M_{n}}$,

where ${\displaystyle n}$ is the average number of surfactant monomers in solution that associate into a micelle, commonly denoted the aggregation number.

The equilibrium is characterized by an equilibrium constant defined by ${\displaystyle K=[M_{n}]/[S]^{n}}$, where ${\displaystyle [M_{n}]}$ and ${\displaystyle [S]}$ are the concentrations of micelles and free surfactant monomers, respectively. In combination with the law of conservation of mass, the system is fully specified by: ${\displaystyle S_{tot}=[S]+nK[S]^{n}}$, where ${\displaystyle S_{tot}}$ is the total surfactant concentration. Phillips[3] defined the CMC as the point corresponding to the maximum change in gradient in an ideal property-concentration (${\displaystyle \phi }$ against ${\displaystyle S_{tot}}$) relationship ${\displaystyle {\frac {d^{3}\phi }{dS_{tot}^{3}}}}$=0. By implicit differentiation of ${\displaystyle S_{tot}=[S]+nK[S]^{n}}$ three times with respect to ${\displaystyle S_{tot}}$ and equating to zero it can be shown[4] that the micellization constant is given by ${\displaystyle K={\frac {n-2}{n^{2}(2n-1)}}\left(CMC\cdot {\frac {2n^{2}-n}{2n^{2}-2}}\right)^{1-n}}$ for ${\displaystyle n>2}$. According to Phillips method the Gibbs free energy change of micellization is therefore given by:

${\displaystyle \Delta G_{micellization}=-{\frac {RT}{n}}\ln \left({\frac {n-2}{n^{2}(2n-1)}}\left(CMC\cdot {\frac {2n^{2}-n}{2n^{2}-2}}\right)^{1-n}\right)}$

The pseudo-phase separation model was originally derived on its own basis, but it has later been shown that it can be interpreted as an approximation to the mass-action model for large ${\displaystyle n}$. That is, for micelles behaving in accordance with the law of mass-action, the pseudo-phase phase separation model is only an approximation and will only become asymptotically equal to the mass-action model as the micelle becomes a true macroscopic phase i.e. for ${\displaystyle n}$→∞. However, the approximation that the aggregation number ${\displaystyle n}$ is large is in most cases sufficient:

${\displaystyle \Delta G_{micellization}\approx RT\ln(CMC)}$

### Ionic micelles

Ionic micelles are typically very affected by the salt concentration. In ionic micelles the monomers are typically fully ionized, but the high electric field strength at the surface of the micelles will cause adsorption of some proportion of the free counter-ions. In this case a chemical equilibrium process can be assumed between the charged micelles ${\displaystyle M_{n}^{-(1-\beta )n}}$ and its constituents, the bile salt monomers, ${\displaystyle S^{-}}$ and bound counter-ions ${\displaystyle B^{+}}$:

${\displaystyle n\cdot S^{-}+\beta \cdot n\cdot B^{+}\rightleftharpoons M_{n}^{-(1-\beta )n}}$

where ${\displaystyle n}$ is the average aggregation number and ${\displaystyle \beta }$ is the average degree of counter-ion binding to the micelle. In this case, the Gibbs free energy is given by:[4]

${\displaystyle \Delta G_{micellization}=-{\frac {RT}{n}}\ln \left({\frac {1}{\left([B^{+}]_{S_{tot}=CMC}\right)^{\beta n}}}{\frac {n-2}{n^{2}(2n-1)}}\left(CMC\cdot {\frac {2n^{2}-n}{2n^{2}-2}}\right)^{1-n}\right)}$

where ${\displaystyle \Delta G_{micellization}}$ is the Gibbs energy of micellization and ${\displaystyle [B^{+}]_{S_{tot}=CMC}}$ is the free counter-ion concentration at CMC. For large ${\displaystyle n}$, that is in the limit when then the micelles becomes a true macroscopic phase, the Gibbs free energy is usually approximated by:

${\displaystyle \Delta G_{micellization}\approx (1+\beta )RT\ln CMC}$

### Dressed micelle model

In the dressed micelle model, the total Gibbs energy is broken down into several components accounting for the hydrophobic tail, the electrostatic repulsion of the head groups, and the interfacial energy on the surface of the micelle.

${\displaystyle \Delta G_{micellization}=\Delta G_{HP}+\Delta G_{EL}+\Delta G_{IF}}$[5]

where the components of the total Gibbs micellization energy are hydrophobic, electrostatic, and interfacial.

## Effect of concentration and temperature

### Solubility and cloud point

Graph showing the CMC

Specific temperature at a specific pressure at which large groups of micelles begin to precipitate out into a quasi-separate phase.[6] As temperature is raised above the cloud point this causes the distinct surfactant phase to form densely packed micelle groups known as aggregates.[6] The phase separation is a reversible separation controlled by enthalpy (promotes aggregation/separation) above the cloud point, and entropy (promotes miscibility of micelles in water) below the cloud point. The cloud point is the equilibrium between the two free energies.[6]

### Critical micelle concentration

The critical micelle concentration (CMC) is the exact concentration of surfactants at which aggregates become thermodynamically soluble in an aqueous solution. Below the CMC there is not a high enough density of surfactant to spontaneously precipitate into a distinct phase.[7] Above the CMC, the solubility of the surfactant within the aqueous solution has been exceeded. The energy required to keep the surfactant in solution no longer is the lowest energy state. To decrease free energy of the system the surfactant is precipitated out. CMC is determined by establishing inflection points for pre-determined surface tension of surfactants in solution. Plotting the inflection point against the surfactant concentration will provide insight into the critical micelle concentration by showing stabilization of phases.[7]

### Krafft temperature

The Krafft temperature is the temperature at which the CMC can be achieved. This temperature determines the relative solubility of surfactant in an aqueous solution. This is the minimum temperature the solution must be at to allow the surfactant to precipitate into aggregates.[8] Below this temperature no level of solubility will be sufficient to precipitate aggregates due to minimal movement of particles in solution.[8] The Krafft Temperature (Tk) is based on the concentration of counter-ions (Caq).[8] Counter-ions are typically in the form of salt. Because the Tk is fundamentally based on the Caq, which is controlled by surfactant and salt concentration, different combinations of the respective parameters can be altered.[8] Although, the Caq will maintain the same value despite changes in concentration of surfactant and salt, therefore, thermodynamically speaking the Krafft temperature will remain constant.[8]

## Surfactant packing parameter

### Differences in shape

Packing Parameter and Micelle Shape

The shape of a surfactant molecule can be described by its surfactant packing parameter, ${\displaystyle N_{\text{S}}}$ (Israelachvili, 1976).[9] The packing parameter takes into account the volume of the hydrophobic chain (${\displaystyle V_{c}}$), the equilibrium area per molecule at the aggregate interface (${\displaystyle a_{e}}$), and the length of the hydrophobic chain (${\displaystyle L_{c}}$):[10]

${\displaystyle N_{\text{S}}={\frac {V_{c}}{a_{e}*L_{c}}}}$[1]

It should also be noted that the packing parameter for a specific surfactant is not a constant. It is dependent on various conditions which affect each the volume of the hydrophobic chain, the cross sectional area of the hydrophilic head group, and the length of the hydrophobic chain. Things that can affect these include, but are not limited to, the properties of the solvent, the solvent temperature, and the ionic strength of the solvent.

### Cone, wedge, and cylinder shaped surfactants

The shape of a micelle is directly dependent on the packing parameter of the surfactant. Surfactants with a packing parameter of ${\displaystyle N_{\text{S}}}$ ≤ 1/3 appear to have a cone-like shape which will pack together to form spherical micelles when in an aqueous environment (top in figure).[10][11] Surfactants with a packing parameter of 1/3 < ${\displaystyle N_{\text{S}}}$ ≤ 1/2 appear to have a wedge-like shape and will aggregate together in an aqueous environment to form cylindrical micelles (bottom in figure).[10][11] Surfactants with a packing parameter of ${\displaystyle N_{\text{S}}}$ > 1/2 appear to have a cylindrical shape and pack together to form a bilayer in an aqueous environment (middle in figure).[10][11]

## Data

Table 1-Common Surfactant Properties
Surfactant Structure CMC (mM) ΔG°${\displaystyle _{micellization}}$ (kJ/mol)
Sodium Dodecyl Sulfate (SDS) 8.2[12] -22.00
Sodium Octyl Sulfate (SOS) -- -14.71
Cetyl Trimethylammonium Bromide (CTAB) 0.89−0.93 [13] -30.46[14]

## References

1. ^ a b c d Butt, Graf, Kappl (2006). Physics and Chemistry of Interfaces. Weinheim: Wiley-VCH. pp. 269–277. ISBN 978-3-527-40629-6.
2. Esumi, Kunio, and Minoru Ueno. Structure-performance Relationships in Surfactants. 2nd ed. Vol. 122. New York: Marcel Dekker, 2003.
3. ^ a b J.N. Phillips. Trans. Faraday Soc. 51 (1955) 561-569
4. ^ a b N.E. Olesen. Journal of Colloid and Interface Science. 453 (2015) 79-89
5. ^ Stokes, Evans (1997). Fundamentals of Interfacial Engineering. New York: Wiley and Sons. p. 222. ISBN 978-0-471-18647-2.
6. ^ a b c Paleologos, Evangelos K.; Giokas, Dimosthenis L.; Karayannis, Miltiades I. (2005). "Micelle-mediated separation and cloud-point extraction". Trends in Analytical Chemistry. 24 (5): 426–436. doi:10.1016/j.trac.2005.01.013.
7. ^ a b Daniel E. Klle, Cary 1. Chlou, Water Solubility Enhancements of DDT and Trichlorobenzene by Some Surfactants Below and Above the Critical Micelle Concentration, Environ. Sci Technol. 1989, 23, 832-838
8. Carolina Vautier-Giongo, Barney L. Bales, Estimate of the Ionization Degree of Ionic Micelles Based on Krafft Temperature Measurements, J. Phys. Chem. B 2003, 107, 5398-5403
9. ^ Israelachvili, Jacob N. (1976). "Theory of self-assembly of hydrocarbon amphiphiles into micelles and bilayers". Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics. 72: 1525–1568.
10. ^ a b c d Cullis, Pieter (1986). "Lipid Polymorphism and the Roles of Lipids in Membranes". Chemistry and Physics of Lipids. 40: 127–144. doi:10.1016/0009-3084(86)90067-8.
11. ^ a b c Borsali, Pecora (2008). Soft-Matter Characterization. Springer. p. 195. ISBN 978-1402044649.
12. ^ P. Mukerjee and K. J. Mysels, "Critical Micelle Concentration of Aqueous Surfactant Systems", NSRDS-NBS 36, US. Government Printing Office, Washington, D.C., 197 1.
13. ^ Wang, Yaofeng (2009). "Encapsulation of Myoglobin in a Cetyl Trimethylammonium Bromide Micelle in Vacuo: A Simulation Study". Biochemistry. 48 (5): 1006–1015. doi:10.1021/bi801952f.
14. ^ Rodriguez, Amalia (2003). "Water-Ethylene Glycol Alkyltrimethylammonium Bromide Micellar Solutions as Reaction Media: Study of Spontaneous Hydrolysis of Phenyl Chloroformate". Langmuir. 19: 7206–7213. doi:10.1021/la0301137.