Abstract

The paper reports the immobilization of Ag+ cations on alumina and silica and AuCl 4 − anions on amino silica and alumina. The method of inverse gas chromatography have demonstrated that Ag(I)-silica is selective for the separation of alkanes, alkenes, alkines, and arenes. The dependence of the capacitance of Ag(I) and Au(III) composites with regard to phenylacetylene (PHA) on the nature of the carriers, surface concentration, and technique of immobilizing ion metals has been considered. The isotherms of the adsorption of PHA from solutions in octane have been measured. It has been revealed that the capacitance of composites with regard to toward PHA prepared by the immobilization of ammoniates of silver nitrate on silicon dioxide is several times higher than for composites based on alumina with the same silver concentration and composites prepared by the immobilization of silver nitrate on silicon dioxide. The capacitance of the Au(III) composite based on alumina for PHA is significantly higher than for that based on aluminum oxide. The highest capacitance for PHA (0.83 and 0.88 molecules per metal ion) is observed for Ag(I) silica and the Au(III) alumina composite. In the visible region, the diffuse reflection spectra of amino silica Au(III) composites have a significant shift of the maximum of adsorption band along with the decrease in the concentration of immobilized anions of AuCl 4 − , which evinces the formation of coordination bonds between free aminipropyl groups of the silica carrier and gold atom. The formation of these bonds prevents the adsorption of PHA on amino silica Au(III) composites with low gold concentrations.

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