The Nernst heat theorem was formulated by Walther Nernst early in the twentieth century and was used in the development of the third law of thermodynamics.
The theorem
editThe Nernst heat theorem says that as absolute zero is approached, the entropy change ΔS for a chemical or physical transformation approaches 0. This can be expressed mathematically as follows:
The above equation is a modern statement of the theorem. Nernst often used a form that avoided the concept of entropy.[1]
Another way of looking at the theorem is to start with the definition of the Gibbs free energy (G), G = H - TS, where H stands for enthalpy. For a change from reactants to products at constant temperature and pressure the equation becomes .
In the limit of T = 0 the equation reduces to just ΔG = ΔH, as illustrated in the figure shown here, which is supported by experimental data.[2] However, it is known from thermodynamics that the slope of the ΔG curve is -ΔS. Since the slope shown here reaches the horizontal limit of 0 as T → 0 then the implication is that ΔS → 0, which is the Nernst heat theorem.
The significance of the Nernst heat theorem is that it was later used by Max Planck to give the third law of thermodynamics, which is that the entropy of all pure, perfectly crystalline homogeneous materials in complete internal equilibrium is 0 at absolute zero.
See also
editReferences and notes
edit- ^ Nernst, Walther (1926). The New Heat Theorem. Methuen and Company, Ltd.- Reprinted in 1969 by Dover - See especially pages 78 – 85
- ^ Nernst, Walther (1907). Experimental and Theoretical Applications of Thermodynamics to Chemistry. New York: Charles Scribner's Sons. pp. 46.
Walther Nernst.
- The labels on the figure have been modified. The original labels were A and Q, instead of ΔG and ΔH, respectively.
Further reading
edit- Denbigh, Kenneth (1971). The Principles of Chemical Equilibrium (3 ed.). Cambridge University Press.- See especially pages 421 – 424