The previously obtained results on sulphate‐water interactions both in liquid and solid states in the four measuring systems (high resolution mixing calorimetry, differntial scanning calorimetry, thermomechanical analysis, and dynamic thermal densimetric analysis) are retrieved according to the universal topoenergetic procedure by considering the solute concentration as governing potential. Ontogenic and phylogenic parameters defining the nature, the overall amplitude, the mass of the kinetic entity and the coupling strength of these interactions, allow to establish the composite structure both of pure water and of aqueous solutions. At least two structures exist in these specimens made from the pure water with isolated molecules and polymerized water molecules involving cations which catalyze H‐bond forming in polymeric chains.