Clay properties sorption isotherms

Quantity/intensity relationships are often used to describe soil capacity to buffer phosphorus concentration in soil pore water. The quantity (0 refers to the amount of phosphorus adsorbed on soil surface, whereas intensity (/) refers to the concentration of P in soil pore water. This ratio can also be viewed as partition coefficient (K ), as indicated by liner sorption isotherms. The ratio expressed as either QII or is influenced by various physicochemical properties of soils, including clay content, high concentration of Fe and Al oxides, CaCOj content, organic matter content, pH, and redox potential. 

The structural characteristics and moisture sorption properties of two kinds of nylon-6/clay hybrids were investigated by Murase et The moisture sorption isotherms of the hybrid samples were a typical sigmoid shape similar to that of the pure nylon-6 sample, even if the extent of moisture regain of the hybrid films was comparatively low. All the isotherms obtained were explained through quantitative analysis in terms of the BET multilayer adsorption theory and complementally with the aid of the FloryHuggins solution theory. 

The amount of adsorbed chemical is controlled by both properties of the chemical and of the clay material. The clay saturating cation is a major factor affecting the adsorption of the organophosphorus pesticide. The adsorption isotherm of parathion from an aqueous solution onto montmorillonite saturated with various cations (Fig. 8.32), shows that the sorption sequence (Al > Na > Ca ) is not in agreement with any of the ionic series based on ionic properties. This shows that, in parathion-montmoriUonite interactions in aqueous suspension, such factors as clay dispersion, steric effects, and hydration shells are dominant in the sorption process. In general, organophosphorus adsorption on clays is described by the Freundhch equation, and the values for parathion sorption are 3 for Ca +-kaoUnite, 125 for Ca -montmorillonite, and 145 for Ca -attapulgite. 

Andrade et al. investigated the transport properties and the solvent induced-crystallization phenomena in poly(ethylene terephthalate) (PET) and PET clay nanocomposites, prepared by melt intercalation. Results of non-isothermal crystallization showed that cold crystallization temperature, and percent of crystallinity of nanocomposites are higher than those of pure PET. The sorption of all die solvents is accompanied by a large-scale stmctural rearrangement, leading to the induced crystallization of the original amorphous state. The solvent induced crystallization caused an increasing of more than four times the percent of crystallinity. 

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