The molecular statistical method for evaluating the distribution of active sites of various adsorbents relative to their energies has been improved. This method is used not only for the treatment of experimental data on the adsorption of hydrocarbons on various adsorbents, which is the usual procedure, but also data on the adsorption of polar water and methanol molecules on the active sites of adsorbent surfaces. Two types of active sites differing in energy have been shown to exist on the surface of graphitized carbon black, the complex shungite carbon/mineral adsorbent, and modified Silochrom. Chromatographic, calorimetric, and structural adsorption data were used to establish the relationship between the observed maxima of the energy distribution function of the adsorption sites with concrete adsorption sites or pores of the surface, on which the molecules are adsorbed.Adsorbents and catalysts, by their nature, are energetically nonhomogeneous. We distinguish between structural and chemical nonhomogeneity. Structural nonhomogeneity for monophase adsorbents is a consequence, for example, of the energy inequivalence of various crystal faces as, for example, in the case of talc [1], the existence of different types of dislocations on the surface of microcrystals, the existence of surface micropores, a breakdown of orderedness in the deposition of adjacent layers in the structure, and the domain distribution of isomorphic impurities.Complex adsorbents such as alumosilica gels, mountain leather-montmorillonite silicates, and carbon-mineral adsorbents are also commonly used in adsorption and catalytic processes. Each of the phases in these adsorbents has a characteristic set of structural-energetic sites of nonhomogeneity, while the boundary of the two adjacent disperse materials is a special type of structural heterogeneity, which plays a role in heterogeneous catalysis.Chemical heterogeneity is related both to the different chemical composition of the adsorbent, which predetermines the type of active adsorption sites, and to their coordination number. Such heterogeneity is characteristic for silica gels with isolated, vicinal, and silanediol groups on the surface [2], for alumina gels with characteristic tetrahedral and octahedral coordination of the surface aluminum atoms, and, correspondingly, different activity of the bound hydroxy groups [3], and for carbon adsorbents with characteristic carboxyl, phenol, and hydroxyl active sites [4].Various physical chemical methods are employed for studying both structural and chemical nonhomogeneity. However, theoretical thermodynamic analysis based on experimental adsorption and chromatographic data remains the most reliable method permitting determination of the quantitative characteristics of surface nonhomogeneity. Various workers [5][6][7] 0040-5760/08/4405-0325