Maxwell Relations

Background

Maxwell’s equations are important for electric and magnetic fields, while Maxwell’s relations focus on thermodynamic quantities like temperature, pressure, volume, and entropy and are important when analyzing thermodynamic systems like internal combustion engines.

Like Maxwell’s equations, Maxwell’s relations are based on partial derivatives. The relations describe the symmetry of second-order partial derivatives of thermodynamic quantities. Maxwell’s relations directly and indirectly cover eight thermodynamic quantities including:

• pressure (P),
• volume (V),
• temperature (T),
• entropy (S) measured in Joules per Kelvin (J/K),
• internal energy (U) measured in Joules,
• enthalpy (H),
• Helmholtz free energy (F or A),
• Gibbs free energy (G).

P, V, and T are simple quantities while the other thermodynamic quantities are more complex, thus Maxwell’s relations are very important.

For example, enthalpy (H) measures a system’s total heat content is defined as the sum of its internal energy (U) plus the product of pressure (P) and volume (V): H = U + PV.

Helmholtz free energy (F) measures the useful work obtainable from a closed system at constant temperature and volume and is defined as F = U – TS.

Gibbs free energy (G) is used to predict the spontaneity of a process at a given temperature and is defined as G = H – TS, or ∂G = ∂H – T∂S:

• When ∂G < 0, the process is spontaneous (favored).
• When ∂G > 0, the process is non-spontaneous (not favored).
• If ∂G = 0, the process is at equilibrium.

Mathematical Derivations of Maxwell's Relations

To derive Maxwell’s relations, it is useful to combine the First and Second Laws into a single mathematical statement. In order to do that, one notes that since:

for a reversible process: dq = TdS

Since: dw = TdS – pdV

for a reversible expansion in which only p-V works is done, and since dU = dq + dw

dU = TdS – pdV         (1)

This differential for dU can be used to simplify the differentials for H, A (Helmholtz energy) and G. But it is even more useful due to the constraints it places on the variables T, S, p and V due to the mathematics of exact differentials. 

Equation 1 suggests that the natural variables of internal energy are S and V or simply U (S, V). Thus, the total differential (dU) in equation 1 can be expressed as follows:

By studying equations 1 and 2, we can see that:

Since dU is an exact differential, the Euler relation must hold that:

substituting equations 3 and 4 into the above expression:

This is an example of a Maxwell Relation.

A similar result can be derived based on the definition of H:

H = U + pV

Using chain rule and differentiating d(pV) results in:

dH = dU + pdV + Vdp

Making the substitution using the combined first and second laws (dU = TdS - pdV) for a reversible change involving on expansion (p-V) work:

dH = TdS – pdV + pdV + Vdp

dH = TdS + Vdp         (5)

As in the case of internal energy, this suggests that the natural variables of H are S and p. Thus, 

If we compare equation 5 and 6 we get:

We can now see that equation 3 and equation 7 are equal to T hence are equal to each other:

Furthermore, the Euler Relation must also hold true:

This is the Maxwell Relation of H. The same can be done for G and A.

Summary

Maxwell Relations are summarized below: