The equilibrium
coefficient obtained by application of the law of mass action to
ion exchange and characterizing quantitatively the ability of an
ion exchanger to select one of two ions present in the same solution. The ions involved in the
exchange should be specified as subscripts. Examples: Exchange:
Mg2+
–
Ca2+
Exchange:
SO42−
–
Cl−
In the above equations subscript S refers to the
ion exchanger ('
stationary phase') and M to the external solution ('
mobile phase'). For exchanges involving
counter-ions differing in their charges, the numerical value of
depends on the choice of the concentration scales in the
ion exchanger and the external solution (
molal scale, molar scale,
mole fraction scale, etc.). Concentration units must be clearly stated for an exchange of ions
of differing charges. The corrected
selectivitycoefficient
(
)
is calculated in a way identical to the
selectivitycoefficient except that the concentrations in the external solutions are replaced by activities.
This term should not be used as a synonym for
separation factor.
Source:
PAC, 1993, 65, 819
(Nomenclature for chromatography (IUPAC Recommendations 1993))
on page 857
PAC, 1993, 65, 2373
(Nomenclature for liquid-liquid distribution (solvent extraction) (IUPAC Recommendations
1993))
on page 2385
Cite as:
IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by
A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997).
XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic,
J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8.
https://doi.org/10.1351/goldbook.