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Various methods for morphological, textural, and structural characterization of polymeric, carbon, and oxide adsorbents have been developed and well described. However, there are ways to improve the quantitative information extraction from experimental data for describing complex sorbents and polymer fillers. This could be based not only on probe adsorption and electron microscopies (TEM, SEM) but also on small-angle X-ray scattering (SAXS), cryoporometry, relaxometry, thermoporometry, quasi-elastic light scattering, Raman and infrared spectroscopies, and other methods. To effectively extract information on complex materials, it is important to use appropriate methods to treat the data with adequate physicomathematical models that accurately describe the dependences of these data on pressure, concentration, temperature, and other parameters, and effective computational programs. It is shown that maximum accurate characterization of complex materials is possible if several complemented methods are used in parallel, e.g., adsorption and SAXS with self-consistent regularization procedures (giving pore size (PSD), pore wall thickness (PWTD) or chord length (CLD), and particle size (PaSD) distribution functions, the specific surface area of open and closed pores, etc.), TEM/SEM images with quantitative treatments (giving the PaSD, PSD, and PWTD functions), as well as cryo- and thermoporometry, relaxometry, X-ray diffraction, infrared and Raman spectroscopies (giving information on the behavior of the materials under different conditions).

Polymer Adsorbents vs. Functionalized Oxides and Carbons: Particulate Morphology and Textural and SurfaceCharacteristics