Clausius-Clapeyron relation

PD Image
The red line in the P-T diagram is the coexistence curve of two phases, I and II, of a single system. Phase II may be the vapor and I the liquid phase of the same compound. The lower green line gives the slope in phase I and the upper green line in phase II.

The Clausius–Clapeyron relation is an equation for a system consisting of two phases of a single compound in thermodynamic equilibrium at constant absolute temperature T and constant pressure P. A curve in a two-dimensional thermodynamical diagram that separates two phases in equilibrium is known as a coexistence curve. The Clausius–Clapeyron relation gives the slope of the coexistence curve in the P-T diagram:

${\frac {\mathrm {d} P}{\mathrm {d} T}}={\frac {Q}{T\,(V^{II}-V^{I})}},$

where Q is the molar heat of transition. It is the heat necessary to bring one mole of the compound from phase I into phase II; it is also known as latent heat. For instance, when phase I is a liquid and phase II is a vapor, then Q ≡ H_v is the molar heat of vaporization. Further, V^I is the molar volume of phase I at the pressure P and temperature T of the point where the slope is considered and V^II is the same for phase II.

The equation is named after Émile Clapeyron, who derived it around 1834, and Rudolf Clausius.

Derivation

The condition of thermodynamical equilibrium at constant pressure P and constant temperature T between two phases I and II is the equality of the molar Gibbs free energies G,

$G^{I}(P,T)=G^{II}(P,T).\,$

The molar Gibbs free energy of phase α (α = I, II) is equal to the chemical potential μ^α of this phase. Hence the equilibrium condition can be written as,

$\mu ^{I}(P,T)=\mu ^{II}(P,T),\;$

which holds along the red (coexistence) line in the figure.

If we go reversibly along the lower and upper green line in the figure, the chemical potentials of the phases change by Δμ^I and Δμ^II, for phase I and II, respectively, while the system stays in equilibrium,

$\mu ^{I}+\Delta \mu ^{I}=\mu ^{II}+\Delta \mu ^{II}\;\Longrightarrow \;\Delta \mu ^{I}=\Delta \mu ^{II}$

From classical thermodynamics it is known that

$\Delta \mu ^{\alpha }(P,T)=\Delta G^{\alpha }(P,T)=-S^{\alpha }\Delta T+V^{\alpha }\Delta P,\quad {\hbox{where}}\quad \alpha =I,II.$

Here S^α is the molar entropy (entropy per mole) of phase α and V^α is the molar volume (volume of one mole) of this phase. It follows that

$-S^{I}\Delta T+V^{I}\Delta P=-S^{II}\Delta T+V^{II}\Delta P\;\Longrightarrow \;{\frac {\Delta P}{\Delta T}}={\frac {S^{II}-S^{I}}{V^{II}-V^{I}}}$

From the second law of thermodynamics it is known that for a reversible phase transition it holds that

$S^{II}-S^{I}={\frac {Q}{T}}$

where Q is the amount of heat necessary to convert one mole of compound from phase I into phase II. Elimination of the entropy and taking the limit of infinitesimally small changes in T and P gives the Clausius-Clapeyron equation,

${\frac {dP}{dT}}={\frac {Q}{T(V^{II}-V^{I})}}$

Approximate solution

The Clausius-Clapeyron equation is exact. When we make the following assumptions we may perform the integration:

• The molar volume of phase I is negligible compared to the molar volume of phase II: V^II >> V^I. In general, far from the critical point, this inequality holds well for liquid-gas transitions.

• Phase II satisfies the ideal gas law

$PV^{II}=RT\,$

If phase II is a gas and the pressure is fairly low this assumption is reasonable.

• The transition heat Q is constant over the temperature integration interval. The integrations run from the lower temperature T₁ to the upper temperature T₂ and from P₁ to P₂.

Under these condition the Clausius-Clapeyron equation becomes

${\frac {dP}{dT}}={\frac {Q}{\frac {RT^{2}}{P}}}\;\Longrightarrow \;{\frac {dP}{P}}={\frac {Q}{R}}\;{\frac {dT}{T^{2}}}$

Integration gives

$\int \limits _{P_{1}}^{P_{2}}{\frac {dP}{P}}={\frac {Q}{R}}\;\int \limits _{T_{1}}^{T_{2}}{\frac {dT}{T^{2}}}\;\Longrightarrow \;\ln {\frac {P_{2}}{P_{1}}}=-{\frac {Q}{R}}\;\left({\frac {1}{T_{2}}}-{\frac {1}{T_{1}}}\right)$

where ln is the natural (base e) logarithm. We reiterate that for gas-liquid transitions Q is the heat of vaporization.