Algebraic conditions, in terms of the solvent partition constants, for the separation of chemical classes by gas–liquid chromatography

<p>The interdependence between the solvation Gibbs energy of several functional groups and the solvent partition coefficients was studied, starting from gas chromatographic data. Single-parameter relationships were derived for the –OH, -CHO, -CO, -O-,-COO (acetate), -COO (methyl ester)-, and -CN group increments. The obtained equations were found to be temperature independent, and could be successfully used for the evaluation of 19 stationary phases with respect to certain separation questions. The selectivity problem was converted into an inequality system. The graphical solution of such a system provides an image of the separation abilities of a sorbent material with respect to a given pair of solutes, and allows an efficient comparison of a great number of stationary phases. The graphs are also illustrative for the temperature effect on the selectivity features.</p