Chemical Sciences: A Manual for CSIR-UGC National Eligibility Test for Lectureship and JRF/Distribution constant


The distribution constant (or partition ratio), is the equilibrium constant for the distribution of an analyte in two immiscible solvents.[1] For a particular solvent, it is equal to the ratio of its molar concentration in the stationary phase to its molar concentration in the mobile phase, also approximating the ratio of the solubility of the solvent in each phase. The term is often confused with partition coefficient or distribution coefficient, and is often represented by KD.

ExpressionEdit

The ratio of activities of a solute, A in an aqueous/organic system will remain constant and independent of the total quantity of A (hence [A]_{org} \propto [A]_{aq}), so at any given temperature:

(K_D)_A = {(a_A)_{org} \over(a_A)_{aq}} \approx {[A]_{org} \over[A]_{aq}}

Distribution constants are useful as they allow the calculation of the concentration of remaining analyte in the solution, even after a number of solvent extractions have occurred. They also provide guidance in choosing the most efficient way to conduct an extractive separation.

Thus, the conentration of A remaining in an aqueous solution after i extractions with an organic solvent can be found using:

[A]_i = ({V_{aq} \over V_{org} K_D + V_{aq}})^i [A]_0

(where [A]i is the concentration of A remaining after extracting Vaq millilitres of solution with the original concentration of [A]0 with i portions of the organic solvent, each with a volume of Vorg).

ReferencesEdit

  1. Rice, N. M.; Irving, H. M. N. H.; Leonard, M. A. (1993), "Nomenclature for liquid-liquid distribution (solvent extraction) (IUPAC Recommendations 1993)", Pure and Applied Chemistry 65: 2373, doi:10.1351/pac199365112373 
Last modified on 5 June 2010, at 02:34