24 Types of Equilibria (Phase, Partition, Etc) (M14Q6)

Learning Objectives

  • Relate various phase equilibria to features of a substance’s phase diagram.

| Key Concepts and Summary | Glossary |

Solid-Liquid & Liquid-Vapor Equilibria

Solid-liquid and liquid-vapor equilibria exist during phase changes, as can be seen below in Figures 1 and 2. In the case of a solid-liquid equilibrium, the rate at which the solid phase is melting is equal to the rate at which the liquid phase is freezing:

H2O(s)  ⇌  H2O(l)

A beaker is full of a colorless, clear liquid. Inside the beaker is a blue cube filled with small blue spheres to represent water molecules. 9 of these spheres are detached and in the clear liquid. There are 6 arrows, 3 showing that the blue spheres are leaving and 3 showing that the detached blue spheres are going to reattach.
Figure 1: Solid-liquid equilibrium, where the rate of freezing is equal to the rate of melting.

In the case of liquid-vapor equilibrium, the rate at which the liquid phase evaporates is equal to the rate at which the gas phase is condensing:

H2O(l)  ⇌  H2O(g)

There is a flask with a black rubber stopper at the top. In the bottom of the flask is a blue, transparent liquid. In the empty space above the liquid, there are 12 blue spheres flying around. There are 6 arrows, 3 showing that detached blue spheres will recombine with the liquid, and 3 showing that a blue sphere will detach from the liquid and float in the empty space.
Figure 2: Liquid-gas equilibrium, where the rate of vaporization is equal to the rate of condensation.

Condensed Phase Equilibria

Condensed phase equilibria occur at the interface between two liquids or two solids. Examples of this are in the phase diagram of SiO2, along the black line between the orange and yellow shaded regions. At any temperature and pressure along this line, there will be an equilibrium between the α- and β- form of quartz, such that the rate of α-quartz converting into β-quartz is equal to the rate of β-quartz converting into α-quartz.

Figure 3: Phase diagram of SiO2.

Solubility Equilibria

Solubility equilibria occur when a solid is dissolved into water. The equilibrium is between the undissolved solid phase and the dissolved aqueous phase of the solid. An example of this is adding glucose (sugar) to water, where so much sugar is added that not all of it dissolves, creating a saturated solution. The rate at which the glucose dissolves is equal to the rate at which the glucose precipitates:

glucose(s)  ⇌  glucose(aq)

Partition Equilibria

Partition equilibria occur when a solute is dissolved in one liquid, a different liquid that is immiscible (will not mix) with the first liquid is added, the mixture is shaken, and the solute moves to the second liquid, as seen in Figure 4 below. Although the majority of the solute may end up in the second liquid, it is important to remember that this is an equilibrium, meaning that the solute will be present in both liquids, but perhaps in different quantities.

In this example, iodine is first dissolved in water. Hexane is carefully added to the system (left picture) and whole container is shaken to mix the liquids together (center picture) and create an equilibrium for iodine dissolved in both liquids:

I2(aq)  ⇌  I2(hexane)

However, water and hexane are immiscible and the two liquids separate once the shaking is complete (right picture). Notice the difference between the left and the right pictures: the colors of the two liquids have changed, reflecting that iodine prefers to be dissolved in hexane. We will learn more about why this phenomenon occurs later in this course when we study intermolecular forces.

This figure has 3 images, each with a separatory funnel. In the left figure, there are two liquids. The bottom is an orange liquid, labeled I 2 (aq). The top liquid is colorless and labeled hexane. The middle figure shows the funnel being shaken and it appears to be a pink liquid. The right figure again has two separate liquids. The bottom is colorless and labeled I 2 (aq). The top is purple and labeled I 2 (hexane). There are equilibrium arrows between these two layers.
Figure 4: (left picture): Iodine dissolved in water and hexane are placed in a flask together. (center picture): The mixture is shaken to combine the two liquids. (right picture): The two layers reform and the iodine is mostly dissolved in the hexane layer.

Key Concepts and Summary

In this section, we look at four types of equilibrium systems. All of these systems differ by which phases are in equilibrium with each other. A solid-liquid or liquid-vapor equilibrium are between the given phases. Condensed phase equilibria are between two of the same phases, either both liquid or both solid. Solubility equilibria have the same molecule as reactant and product, except the reactant is in the solid phase and the product are the dissolved aqueous ions. Partition equilibria again have the same molecule as reactant and product, except the molecule is dissolved in different liquids between the reactants and products.

Glossary

condensed phase equilibria
equilibrium system that occurs at the interface between two liquids or two solids

partition equilibria
equilibrium system that occurs when an immiscible liquid is added to another liquid with a dissolved solute. When the mixture is shaken, some of the solute moves from the first liquid to the added liquid.

solid-liquid, liquid-vapor equilibria
equilibrium system that occurs at the interface between a solid and liquid phase or a liquid and gas phase

solubility equilibria
equilibrium system that occurs when a solid is dissolved into water, solid ⇌ aqueous

License

Icon for the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License

CHEM 104: Working Copy Copyright © by Chem 104 Textbook Team is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, except where otherwise noted.

Share This Book

Feedback/Errata

Leave a Reply

Your email address will not be published. Required fields are marked *