Abstract
The significance and metrological meaning of parameters accessible to regressive estimates from the experimental data on solubility polytherms are refined using corollaries to the universal interrelation between the Gibbs energy, enthalpy, and entropy of dissolution. A standard procedure for processing solubility polytherms is suggested. Its informativeness is illustrated for the example of new metrologically verified data on the polytherm of solubility of ferrocene in pure water.
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