We report on a new approach for the synthesis of TiO₂-pillared montmorillonite, where the pillars exhibit a high degree of crystallinity (nanocrystals) representing a mixture of anatase and rutile phases. The structures exhibit improved adsorption and photocatalytic activity as a result of hydrothermally activated intercalation of titanium polyhydroxo complexes (i.e., TiCl₄ hydrolysis products) in a solution with a concentration close to the sol formation limit. The materials, produced at various annealing temperatures from the intercalated samples, were characterized by infrared spectroscopy, differential scanning calorimetry (DSC)/thermogravimetric analysis (TGA), X-ray diffraction, dynamic light scattering (DLS) measurements, and liquefied nitrogen adsorption/desorption. The photocatalytic activity of the TiO₂-pillared materials was studied using the degradation of anionic (methyl orange, MO) and cationic (rhodamine B, RhB) dyes in water under UV irradiation. The combined effect of adsorption and photocatalysis resulted in removal of 100% MO and 97.5% RhB (with an initial concentration of 40 mg/L and a photocatalyst-sorbent concentration of 1 g/L) in about 100 minutes. The produced TiO₂-pillared montmorillonite showed increased photocatalytic activity as compared to the commercially available photocatalyst Degussa P25.

Photocatalytic, plasma and combined plasma–photocatalytic processes were applied for the destruction of a model pollutant, Rhodamine B dye, in an aqueous solution (concentration of 40 mg/L). For this purpose TiO₂-pillared montmorillonite was used as a photocatalyst (characterized by X-ray analysis and low-temperature nitrogen adsorption/desorption). It was prepared by the method of intercalation of titanium hydroxocomplexes, including hydrothermal activation of the process and preliminary mechanical treatment of the layered substrate. The dielectric barrier discharge (DBD) plasma in the presence of photocatalysts increases the efficiency of dye degradation (100%, 8 s) compared to plasmolysis (94%) and UV photolysis (92%, 100 min of UV irradiation); in contrast to photolysis, destructive processes are more profound and lead to the formation of simple organic compounds such as carboxylic acids. The plasma–catalytic method enhances by 20% the energetic efficiency of the destruction of Rhodamine B compared to DBD plasma. The efficiency of dye destruction with the plasma–catalytic method increases with the improvement of the textural properties of the photocatalyst.

The molecular and ionic composition of vapor over lanthanum tribromide was studied by high-temperature mass spectrometry under the conditions of sublimation from a Knudsen effusion cell and from an open single crystal surface. The partial pressures of LaBr₃ and La₂Br₆ in saturated vapor and the ratio between their sublimation coefficients under free vaporization conditions were determined. The second and third laws of thermodynamics were used to calculate the enthalpies of sublimation of LaBr₃ in the form of monomers and dimers. In ionic sublimation studies, the emission of the Br⁻, LaBr ⁻₄ , and La_2Br ^t-₇ negative ions was recorded in both regimes. Studies of the ionic sublimation of LnX₃ single crystals were shown to give reliable data on the thermochemical properties of negative ions.