Abstract

In this paper, we dilatometrically studied the elastoplastic properties of spherical grains of industrial weakly acidic and strongly acidic ion-exchanger in experiments with constant uniaxial compression and a subsequent unload at room temperature, depending on the ionic form and concentration of the electrolyte solution. It was found that the ionic form of polyacrylate and polymethacrylate cross-linked with triethylene glycol dimethacrylate and divinylbenzene, respectively, and the concentration of the external solution affects their elastoplastic properties. In dilute solutions of sodium chloride and calcium chloride, the gels exhibited elastic properties with close relative amplitudes of deformation. The amplitude of deformation of the grain of polymethacrylate crosslinked with divinylbenzene, in the Ni form, in a dilute nickel chloride solution was significantly lower than that of the Ca form, with significant plastic deformation. With an increasing concentration of the external solution of calcium and nickel chlorides under mechanical load on the grain of polymethacrylate cross-linked with divinylbenzene, the total deformation of the granule and the magnitude of elastic deformation decreased, while the residual (plastic) deformations increased. In concentrated solutions of CaCl2 and NiCl2, such an ion-exchanger became an inelastic rigid material. Even under increased mechanical load, the magnitude of its elastic compressive deformation was very small. The K-form of a swollen in water strongly acidic polystyrene cation-exchanger with grafted sulpho groups cross-linked with divinylbenzene is also characterized by elastic deformations, i.e. the polymer is in a highly elastic state. However, the polystyrene matrix is more rigid compared to polyacrylic and polymethacrylic cation-exchangers in the alkali metal ion form, so the amplitude of deformation is significantly smaller. For such a cation-exchanger in Ca- and Ni- forms, elastic deformations prevail even in concentrated solutions.

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