# Phase separation

Entry by Emily Redston, AP 225, Fall 2011

We typically talk about phase separation in terms of the regular solution model of liquids. The free energy of mixing can be written as,

<math>V</math> represents bond energies, <math>z</math> is the number of neighbors, <math>N</math> is the total number of atoms, and <math>x</math> is the mole fraction. The sign of <math>\epsilon</math> is essential in determining the solution's behavior as a function of temperature. If <math>\epsilon</math> < 0 then the change in free energy upon mixing is always negative, so the atoms will always want to be fully mixed. For <math>\epsilon</math> > 0, there is a temperature dependance, and either mixing or phase separation can occur. Figure 1 shows a plot of <math>G_{mix}</math>/<math>RT</math> versus composition for various values of <math>\epsilon</math>/<math>RT</math>.

For <math>\epsilon</math>/<math>RT</math> values < 2, we can see that the curve only has a single minimum. Let's look at the schematic of this in Figure 2(a). This shows that homogeneous mixture of the components is the stable equilibrium state. We can immediately see this by comparing the free energy of the homogenous solution of composition <math>\phi_0</math> with that of a heterogeneous mixture of two phases of arbitrary compositions <math>\phi_1</math> and <math>\phi_2</math>. The free energy of the heterogeneous mixture is the sum of the free energies of the volume fractions of the constituent phases corresponding to the point <math>F_{sep}</math>. It is clear that the free energy of the mixture <math>F_{sep}</math> is higher that that of the solution <math>F_0</math>. Thus the homogeneous phase is thermodynamically stable; for any composition, the system is at a lower free energy when fully mixed than it would be if it separated into two different compositions. However, for <math>\epsilon</math>/<math>RT</math> values ≥ 2, something quite different occurs because the curve has two minima. Now we consider the schematic diagram in Figure 2(b). The solution can lower its energy from <math>F_0</math> to <math>F_{sep}</math> by separating into two phases <math>\phi_1</math>/<math>\phi_2</math>. The state of lowest energy <math>F_{sep}</math> corresponds to the common tangent to the curve at the points <math>\phi_1</math>/<math>\phi_2</math>. Imagine you are sitting at the composition corresponding to the maximum of the curve: you can immediately see that it is possible for the system can lower its free energy by separating into compositions at the two minima rather than staying as a homogenous mixture. Thus any composition in this region will spontaneously separate into two phases --- this is known as **phase separation**!

We can define this more explicitly for our regular solution model by saying that phase separation occurs when

By taking this derivative and solving for <math>T_{P}</math> (below which phase separation occurs), we will define a phase boundary on our temperature versus composition phase diagram (Figure 3).

We can also define a critical point in the temperature,<math>T_c</math>, which is the maximum temperature below which phase separation will occur (the maximum of the <math>T_P</math> curve). This will occur at <math>x_A = 0.5</math>.

We can find the proportions of both phases in our 2-phase region can be found using the "lever rule". From here, we can also go on to consider spinodal lines.

See also:

Phase separation in Phases and Phase Diagrams from Lectures for AP225.

## References

[1] Spaepen, Frans. *Applied Physics 282: Solids: Structure and Defects*. Harvard University

[2] Haasen, Peter. *Physical Metallurgy*. Cambridge: Cambridge UP, 1996.

## Keyword in References

The Role of Polymer Polydispersity in Phase Separation and Gelation in Colloid−Polymer Mixtures