Clausius-Clapeyron Equation
Why it matters in thermodynamics and process design
The Clausius-Clapeyron equation links vapor pressure, temperature, and enthalpy of vaporization. It is widely used to estimate pressure-temperature behavior in evaporation, distillation, and safety analysis.
As temperature rises, saturation vapor pressure can increase strongly. The equation provides a practical approximation for process planning, equipment operation, and condition screening in laboratory and industrial workflows.
- Estimate vapor pressure at a new temperature
- Determine ΔHvap from measured data points
- Find target temperature for a required vapor pressure
Formulas (MathJax)
R = 8.314 J·mol⁻¹·K⁻¹; ΔHvap in kJ/mol is internally converted to J/mol.
Formula symbol legend
- P₁, P₂ = vapor pressure at T₁ and T₂
- T₁, T₂ = absolute temperature in Kelvin
- ΔHvap = molar enthalpy of vaporization
- R = universal gas constant
- ln = natural logarithm
Detailed examples
Given P₁ = 1.013 bar at T₁ = 373.15 K, ΔHvap = 40.66 kJ/mol, and T₂ = 393.15 K.
Result: P₂ increases substantially above 1 bar, showing strong temperature sensitivity.
Using two measured pressure-temperature pairs, ΔHvap can be back-calculated.
This is useful for fluid characterization in lab practice and teaching.
Given P₁, T₁, ΔHvap, and required P₂, solve for T₂ directly.
Helpful for process setpoint planning in evaporation and distillation.
• Always use Kelvin.
• Use consistent pressure units for P₁ and P₂.
• Approximation quality is best over moderate temperature ranges with near-constant ΔHvap.
Deeper context
Model assumptions
The integrated Clausius-Clapeyron form assumes approximately constant ΔHvap over the selected range and sufficiently ideal vapor behavior. For broader ranges, higher-fidelity property models may be required.
Engineering relevance
From vacuum drying to distillation and pressure safety checks, pressure-temperature dependence governs operation windows. Clausius-Clapeyron remains a core first-pass model for rapid engineering estimates.
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