Broad visible emissions dominant at green or red have been observed for the thermally-treated Ag(+) exchanged SOD zeolites, determined by the Ag(+) loading contents and the excitation wavelengths. Contrary to the notable reversible green/red dominant emission evolution in the Ag(+) exchanged LTA zeolites upon hydration/dehydration in air (or water vapor)/vacuum, emission spectra of the Ag(+) exchanged SOD zeolites are insensitive to the environmental change. This is most probably due to the difficult H2O permeation in SOD zeolites in comparison with LTA zeolites. By combining the environment dependent emission spectra of the Ag(+) exchanged LTA and SOD zeolites, we proposed the following emission mechanisms for Ag(+) exchanged LTA and SOD zeolites: the green emission is due to the transition from ligand-to-metal (framework O(2-)→ Ag(+)) charge transfer state to the ground state and the red emission is due to the transition from the metal-metal (Ag(+)-Ag(+)) charge transfer state to the ground state. The insensitive environment dependent emission characteristics of Ag(+) exchanged SOD zeolites may have potential applications as robust phosphors.

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The possibility of producing complex-profile thin-walled sorbents based on synthesized zeolite is investigated. It is proposed to use natural aluminosilicate as binders. Methods have been developed for controlling properties of zeolite-based molding mixtures by introducing a plasticizer or by alkali or acid modifying the binder structure.

LTA zeolite can be prepared from dry mixes in a vibratory mill with an impact-shear loading conditions. For the synthesis of LTA zeolite, it is necessary to use the anhydrous ingredients (Al 2 Si 2 O 7 -metakaolin, c-Al 2 O 3 ). The process of synthesis is controlled by X-ray diffraction, IR-spectroscopy, and atomic-force microscopy. The presence of structural water in the initial ingredients (Al 2 Si 2 (OH) 4 -kaolin or Al(OH) 3 ) leads to the formation of feldshpatoids (nepheline, sodalite). It was established that the process of mechanical activation requires the synthesis of sodium aluminate of cubic and/or tetragonal crystal systems with a lattice parameters close to those for LTA zeolite. These sodium aluminate acts as a steric template for an ''assembly'' of the zeolite. The presence of sodium aluminate with some other crystal structure results in the formation of sodalite. There is an optimal time of mechanochemical activation, which is determined by the synthesis of sodium aluminate with cubic or tetragonal crystal structure. A model of the mechanochemical synthesis of LTA zeolite was proposed.

It was studied the effect of ultrasonic processing (22kHz) of the aqueous suspension of metakaolin, sodium hydroxide and alumina with a molar ratio 2Al2Si2O7:12NaOH:2Al2O3 on the low-modulus zeolite synthesis processes. To investigate the XRD, SEM, IR, EDS had been used. It was shown that after ultrasonic processing, sodium aluminates are formed, what leads to a change in process of further synthesis. It was found that without ultrasonic processing on the stage of thermal treatment at 650°C, SOD zeolite (|Na6|[Al6Si6O24]) and sodium aluminosilicate (Na6Al4Si4O17) are synthesized. In the sample after ultrasound during thermal treatment, only sodium aluminosilicates of cubic syngony (Na6Al4Si4O17 and Na8Al4Si4O18) are formed. It was demonstrated that sodium aluminosilicates are precursors for the formation of LTA zeolite (|Na12|[Al12Si12O48]). As a result zeolitization of sodium aluminosilicates after the hydrothermal crystallization in alkaline solution, the sonicated sample contained 97wt% LTA. Without ultrasonic processing, the product of synthesis contained 50wt% SOD and 40wt% LTA.