Extractive distillation

Such mixtures cannot be separated by simple distillation, because the volatility of the two components in the mixture is nearly the same, causing them to evaporate at nearly the same temperature at a similar rate, making normal distillation impractical.

The solvent interacts differently with the components of the mixture thereby causing their relative volatilities to change.

The solvent must alter the relative volatility by a wide enough margin for a successful result.

The solvent should be easily separable from the bottom product, and should not react chemically with the components or the mixture, or cause corrosion in the equipment.

A classic example to be cited here is the separation of an azeotropic mixture of benzene and cyclohexane, where aniline is one suitable solvent.

Process flow diagram showing an extractive distillation apparatus. In this case the mixture components A and B are separated in the first column through the solvent E (recovered in the second column).