Based on the CPC's and solvents' Hansen solubility parameters the affinity between CPC and solvent represented by the distance in Hansen space was determined. As a second parameter the molar volume of the solvent molecules was used to describe the selectivity of the CPC by means of a quarter circle like area clearly separating 鈥済ood鈥?and 鈥渂ad鈥?solvents in a so-called solvent map.
Whereas the Hansen solubility parameters are based on thermodynamics, the influence of the solvents' molar volume on the CPC's selectivity can be explained by diffusion processes. When increasing the molar volume of solvents having a similar chemical structure, a limiting value of the molar volume was found above which no solvent diffusion into the CPC was observed.
Using this large number of solvents it could be clearly shown that the electrical response kinetics upon immersion into 鈥済ood鈥?solvents cannot be correlated with the Hansen solubility parameters of the CPC or their difference between CPC and solvent but is determined by the diffusion kinetics, which is governed by the solvents molecule size.