Мastering and modernization of physico-chemical processes of synthesis of oxide compounds with structure of pyrochlorine

Modern scientific and technological development of society, further intensification of production together with the provision of proper safety of human life and preservation of the environment necessitate the search for new solutions in the creation of new materials and technologies. The creation of effective materials for the latest and future technologies and technicaldevices is based on new scientific data on the definition and analysis of specific mechanisms of physicochemical processes that implement the desired structural and phase state of solids with the desired set of properties. In recent decades, the most effective way to control the properties of solid materials is the use of nanotechnology and nanomaterials, which have recently been increasingly used in almost all areas of new technologies. The article investigates synthesis processes, structural characteristics and structural-phase processes in multicomponent metal-ceramic oxide materials, physicochemical mechanisms ofsynthesi s of multielement oxide compounds Y2Zr2O7 with pyrochlor structure during consolidation and sintering of yttrium and zirconium oxides, structure formation -phase characteristics of materials with different chemical composition. The structural-phase evolution in the synthesis of new substances and the consolidation of compounds of the Y2O3 – ZrO2 system have been studied. Samples of oxide heat with the proportion of pyrochlorine phase Y2Zr2O7 up to 41 % were obtained. It is established that the kinetics of increasing the proportion of pyrochlorine phase in the samples indicates a desirable increase in the activity of the chemical reaction, which can be achieved by increasing the synthesis temperature to the temperatures of eutectic formation or increasing the reaction surface of powders.

Solid-phase synthesis of ytterbium zirconate using mechanical activation

Nanocrystalline ytterbium zirconate Yb4Zr3O12 was prepared by the solid-phase method using mechanical activation of stoichiometric mixture of zirconium and ytterbium oxides. Mechanical activation was carried out in an AGO-2 centrifugal-planetary mill at a centrifugal factor of 40 g for 10 min. The processes occurring during the calcination of the mechanically activated mixture of ytterbium and zirconium oxides in the range from 600 to 1300 °C were investigated using X-ray phase analysis, IR spectroscopy, and complex thermal analysis.

Production of corundum armored ceramics

The purpose of this study was to develop the compositions and technology of corundum armored ceramics with high ballistic characteristics based on aluminum oxide with an α-Al2O3 content of more than 99 wt.%. The results of the study of the physicochemical processes of obtaining corundum ceramics modified with complex additives consisting of magnesium - aluminosilicate eutectic mixture and oxides of magnesium, yttrium, titanium, zirconium are presented. The introduction of complex additives into the composition of corundum ceramics provides a significant reduction (100-150°C) of the sintering temperature of the product. In this case, additives of yttrium and zirconium oxides contribute to the formation of a uniform-grained microstructure of ceramics, and in the case of adding titanium oxide, a collective recrystallization of corundum grains is noted. The use of small additives (0.3-0.5 wt.%) of magnesium and yttrium oxides together with a eutectic mixture in the compositions of corundum ceramics based on high-quality alumina contributes to the formation of a uniform-grained, dense structure of the material and giving it a high level of physical and mechanical properties as a result of directional the action of each component of the additive on the physicochemical processes of phase formation of the crystalline matrix. A model idea of the mechanism of action of additives on the formation of the microstructure of ceramics during stage-by-stage heating from 1350 to 1650°C in the sintering mode of products is presented. The developed compositions and technologies of corundum armored ceramics have a production focus and implementation in practice.

Pure and Sb-doped ZrO2 for removal of IO3− from radioactive waste solutions

Radioactive 129I with a long half-life (1.57 × 107 y) and high mobility is a serious radiohazard and one of the top risk radionuclides associated with its accidental and planned releases to nature. The complex speciation chemistry of iodine makes its removal a complicated task, and usually a single method is not able to remove all iodine species. Especially its oxidized form iodate (IO3−) lacks a selective and effective removal method. Here, the granular aggregates of hydrous zirconium oxides with and without antimony doping were tested for IO3− removal and the effects of contact time, competing anions in different concentrations and pH were examined. The materials showed high selectivity for IO3− (Kd over up to 50,000 ml/g) in the presence of competing ions and relatively fast uptake kinetics (eq. < 1 h). However, B(OH)4− and SO42−, as competing ions, lowered the iodate uptake significantly in basic and acidic solution, respectively. The suitability of the materials for practical applications was tested in a series of column experiments where the materials showed remarkably high apparent capacity for the IO3− uptake (3.2–3.5 mmol/g). Graphic abstract

Mechanical and Magnetic Properties of Double Layered Nanostructures of Tin and Zirconium Oxides Grown by Atomic Layer Deposition

Double layered stacks of ZrO2 and SnO2 films, aiming at the synthesis of thin magnetic and elastic material layers, were grown by atomic layer deposition to thicknesses in the range of 20–25 nm at 300 °C from ZrCl4, SnI4, H2O, and O3 as precursors. The as-deposited nanostructures consisted of a metastable tetragonal polymorph of ZrO2, and a stable tetragonal phase of SnO2, with complementary minor reflections from the orthorhombic polymorph of SnO2. The hardness and elastic modulus of the stacks depended on the order of the constituent oxide films, reaching 15 and 171 GPa, respectively, in the case of top SnO2 layers. Nonlinear saturative magnetization could be induced in the stacks with coercive fields up to 130 Oe.