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This article deals with melting and freezing point depression due to mixture of another compound. For depression due to small particle size, see melting point depression.

Freezing-point depression describes the phenomenon in which the freezing point of a liquid (a solvent) is depressed when another compound is added, meaning that a solution has a lower freezing point than a pure solvent. This happens whenever a solute is added to a pure solvent, such as water. The phenomenon may be observed in sea water, which due to its salt content remains liquid at temperatures below 0 °C, the freezing point of pure water.



The change in chemical potential of a solvent when a solute is added explains why freezing point depression takes place.

The freezing point depression is a colligative property, which means that it is dependent on the presence of dissolved particles and their number, but not their identity. It is an effect of the dilution of the solvent in the presence of a solute. It is a phenomenon that happens for all solutes in all solutions, even in ideal solutions, and does not depend on any specific solute-solvent interactions. The freezing point depression happens both when the solute is an electrolyte, such as various salts, and a nonelectrolyte. In thermodynamic terms, the origin of the freezing point depression is entropic and is most easily explained in terms of the chemical potential of the solvent.

At the freezing (or melting) point, the solid phase and the liquid phase have the same chemical potential meaning that they are energetically equivalent. The chemical potential is dependent on the temperature, and at other temperatures either the solid or the liquid phase has a lower chemical potential and is more energetically favourable than the other phase. In many cases, a solute does only dissolve in the liquid solvent and not in the solid solvent. This means that when such a solute is added, the chemical potential in the liquid phase is decreased by dilution, but the chemical potential of the solvent in the solid phase is not affected. This means in turn that the equilibrium between the solid and liquid phase is established at another temperature for a solution than a pure liquid; i.e., the freezing point is depressed.[1]

The phenomenon of boiling point elevation is analogous to freezing point depression. However, the magnitude of the freezing point depression is larger than the boiling point elevation for the same solvent and the same concentration of a solute. Because of these two phenomena, the liquid range of a solvent is increased in the presence of a solute.


The extent of freezing-point depression can be calculated by applying the Clausius-Clapeyron relation and Raoult's law together with the assumption of the non-solubility of the solute in the solid solvent. The result is that in dilute ideal solutions, the extent of freezing-point depression is directly proportional to the molal concentration of the solution according to the equation[1]

ΔTf = Kf · mB


  • ΔTf, the freezing point depression, is defined as Tf (pure solvent)Tf (solution), the difference between the freezing point of the pure solvent and the solution. It is defined to assume positive values when the freezing point depression takes place.
  • Kf, the cryoscopic constant, which is dependent on the properties of the solvent. It can be calculated as Kf = RTm2MHf, where R is the gas constant, Tm is the melting point of the pure solvent in kelvins, M is the molar mass of the solvent, and ΔHf is the heat of fusion per mole of the solvent.
  • mB is the molality of the solution, calculated by taking dissociation into account since the freezing point depression is a colligative property, dependent on the number of particles in solution. This is most easily done by using the van 't Hoff factor i as mB = msolute · i. The factor i accounts for the number of individual particles (typically ions) formed by a compound in solution. Examples:
    • i = 1 for sugar in water
    • i = 2 for sodium chloride in water, due to dissociation of NaCl into Na+ and Cl-
    • i = 3 for calcium chloride in water, due to dissociation of CaCl2 into Ca2+ and 2 Cl-
    • i = 2 for hydrogen chloride in water, due to complete dissociation of HCl into H+ and Cl-
    • i = 1 for hydrogen chloride in benzene, due to no dissociation of HCl in a non-polar solvent

At high concentrations, the above formula is less precise due to the approximations used in its derivation and any nonideality of the solution. If the solute is highly soluble in the solid solvent, one of the key assumptions used in deriving the formula is not true. In this case the effect of the solute on the freezing point must be determined from the phase diagram of the mixture.

Cryoscopic constants

Values of the cryoscopic constant Kf for selected solvents:[2][3]

Compound Freezes at °C Kf at °C/m
Acetic acid 16.6 3.90
Benzene 5.5 5.12
Camphor 179.8 39.7
Carbon disulfide −112 3.8
Carbon tetrachloride −23 30
Chloroform −63.5 4.68
Cyclohexane 6.4 20.2
Ethanol −114.6 1.99
Ethyl ether −116.2 1.79
Naphthalene 80.2 6.9
Phenol 41 7.27
Water 0 1.86


The phenomenon of freezing point depression is used in technical applications to avoid freezing. In the case of water, ethylene glycol or other forms of antifreeze is added to cooling water in internal combustion engines, making the water stay a liquid at temperatures below its normal freezing point.

The use of freezing-point depression through "freeze avoidance" has also evolved in some animals that live in very cold environments. This happens through permanently high concentration of physiologically rather inert substances such as sorbitol or glycerol to increase the molality of fluids in cells and tissues, and thus decrease the freezing point. Examples include some species of arctic-living fish, such as rainbow smelt, which need to be able to survive in freezing temperatures for a long time. In other animals, such as the spring peeper frog (Pseudacris crucifer), the molality is increased temporarily as a reaction to cold temperatures. In the case of the peeper frog, this happens by massive breakdown of glycogen in the frog's liver and subsequent release of massive amounts of glucose.[4]

Together with formula above, freezing-point depression can be used to measure the degree of dissociation or the molar mass of the solute. This kind of measurement is called cryoscopy (Greek "freeze-viewing") and relies on exact measurement of the freezing point. The degree of dissociation is measured by determining the van 't Hoff factor i by first determining mB and then comparing it to msolute. In this case, the molar mass of the solute must be known. The molar mass of a solute is determined by comparing mB with the amount of solute dissolved. In this case, i must be known, and the procedure is primarily useful for organic compounds using a nonpolar solvent. Cryoscopy is no longer as common a measurement method as it once was. As an example, it was still taught as a useful analytic procedure in Cohen's Practical Organic Chemistry of 1910,[5] in which the molar mass of Naphthalene is determined in a so-called Beckmann freezing apparatus.

Freezing-point depression can also be used as a purity analysis tool when analysed by Differential scanning calorimetry.[6] The results obtained are in mol%, but the method has its place, where other methods of analysis fail.

This is also the same principle acting in the melting-point depression observed when the melting point of an impure solid mixture is measured with a melting point apparatus, since melting and freezing points both refer to the liquid-solid phase transition (albeit in different directions).

In principle, the boiling point elevation and the freezing point depression could be used interchangeably for this purpose. However, the cryoscopic constant is larger than the ebullioscopic constant and the freezing point is often easier to measure with precision, which means measurements using the freezing point depression are more precise.

See also


  1. ^ a b P. W. Atkins and J. de Paula, Atkins' Physical Chemistry, 7th Ed., Oxford University Press, Oxford, 2002, ISBN 0-19-879285-9, p. 175-177
  2. ^ P. W. Atkins, Physical Chemistry, 4th Ed., p. C17 (Table 7.2)
  3. ^ Molare Schmelzpunkterniedrigung, article in German Wikipedia
  4. ^ L. Sherwood et al., Animal Physiology - From Genes to Organisms, 2005, Thomson Brooks/Cole, Belmont, CA, ISBN 0-534-55404-0, p. 691-692
  5. ^ Julius B. Cohen Practical Organic Chemistry 1910 Link to online text
  6. ^ "DSC Purity Analysis". Retrieved 2009-02-05. 

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