Question:

In liquid-liquid extraction, the distribution coefficient D is defined as:

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Always remember that distribution coefficients are temperature-dependent.
Operating temperature must be maintained constant during extraction to ensure stable and predictable distribution behaviour.
Updated On: Jul 3, 2026
  • Concentration in extract / Concentration in raffinate
  • Concentration in feed / Concentration in solvent
  • Mole fraction in heavy phase / light phase
  • Activity coefficient ratio
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The Correct Option is A

Solution and Explanation

Step 1: Understanding the Question:
The question asks for the thermodynamic definition of the distribution coefficient (or partition coefficient, \( D \)) in liquid-liquid extraction.

Step 2: Key Formula or Approach:
Liquid-liquid extraction involves separating a solute from a liquid feed by contacting it with an immiscible solvent phase.
At equilibrium, the solute distributes itself between the two phases (the solvent-rich extract phase and the diluent-rich raffinate phase) according to the distribution coefficient:
\[ D = \frac{C_E}{C_R} \]
where \( C_E \) is the solute concentration in the extract phase, and \( C_R \) is the solute concentration in the raffinate phase.

Step 3: Detailed Explanation:

Extract Phase: The phase containing the solvent and the extracted solute.

Raffinate Phase: The residual liquid feed phase from which the solute has been removed.

Distribution Coefficient Significance: The value of \( D \) measures the solvent's affinity for the solute.
A high distribution coefficient (\( D \gt 1 \)) is desirable because it means less solvent is required to achieve a specified separation.
If \( D \lt 1 \), the solute has a higher affinity for the feed diluent, making extraction difficult.

Selectivity comparison: The separation efficiency is also governed by selectivity (\( \beta \)), which is the ratio of the distribution coefficient of the solute to that of the diluent.


Step 4: Final Answer:
The distribution coefficient is defined as the concentration of solute in the extract phase divided by the concentration of solute in the raffinate phase.
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