Influence of the Change of Phase Composition of (1 - x)ZrO2-xAl2O3 Ceramics on the Resistance to Hydrogen Embrittlement.

The article describes the influence of the change in the phase composition of ceramics on the stability of the crystal structure and retention of thermo-physical parameters during hydrogenation of the surface layer in the proton irradiation process. The selection of irradiation conditions allows modeling the degradation processes of ceramics associated with gas swelling during hydrogenation, as well as revealing the patterns of the effect of phase composition on embrittlement, de-strengthening, and structural degradation resistance. In the course of the conducted studies, dose-dependencies of irradiation-induced structural changes and consecutive accumulation of radiation-induced damage in ceramics as a result of hydrogenation of the damaged near-surface layer were established. It was found that the maximum structural changes are observed at doses above 1015 protons/cm2. Dependencies of the change in the degree of structural order as a function of the dose of accumulated damage and the concentration of accumulated protons were obtained. It was established that the variation of the ceramics phase composition due to the formation of solid solutions of ZrO2/Al2O3 and ZrO2/Al2O3/AlZr3 type leads to an enhancement of resistance to swelling by 3-5 times in comparison with monoclinic ZrO2 ceramics. The general analysis of the variation of strength and thermo-physical parameters of ceramics as a function of irradiation fluence for ceramics with different phase compositions showed a direct dependence of the decrease in hardness, resistance to cracking, and thermal conductivity on the concentration of deformation structural distortions caused by irradiation.

Synthesis and Characterization of the Properties of (1-x)Si3N4-xAl2O3 Ceramics with Variation of the Components.

The aim of this paper is to study the effect of variation in the component ratio of (1-x)Si3N4-xAl2O3 ceramics on the phase composition, strength and thermal properties of ceramics. To obtain ceramics and their further study, the solid-phase synthesis method combined with thermal annealing of samples at a temperature of 1500 °C typical for the initialization of phase transformation processes was used. The relevance and novelty of this study lies in obtaining new data on the processes of phase transformations with a variation in the composition of ceramics, as well as determining the effect of the phase composition on the resistance of ceramics to external influences. According to X-ray phase analysis data, it was found that an increase in the Si3N4 concentration in the composition of ceramics leads to a partial displacement of the tetragonal phase of SiO2 and Al2(SiO4)O and an increase in the contribution of Si3N4. Evaluation of the optical properties of the synthesized ceramics depending on the ratio of the components showed that the formation of the Si3N4 phase leads to an increase in the band gap and the absorbing ability of the ceramics due to the formation of additional absorption bands from 3.7-3.8 eV. Analysis of the strength dependences showed that an increase in the contribution of the Si3N4 phase with subsequent displacement of the oxide phases leads to a strengthening of the ceramic by more than 15-20%. At the same time, it was found that a change in the phase ratio leads to the hardening of ceramics, as well as an increase in crack resistance.

Evaluation of the Influence of Grain Sizes of Nanostructured WO3 Ceramics on the Resistance to Radiation-Induced Softening.

The main purpose of this study is to test a hypothesis about the effect of grain size on the resistance to destruction and changes in the strength and mechanical properties of oxide ceramics subjected to irradiation. WO3 powders were chosen as objects of study, which have a number of unique properties that meet the requirements for their use as a basis for inert matrices of dispersed nuclear fuel. The grain-size variation in WO3 ceramics was investigated by mechanochemical grinding of powders with different grinding speeds. Grinding conditions were experimentally selected to obtain powders with a high degree of size homogeneity, which were used for further research. During evaluation of the strength properties, it was found that a decrease in the grain size leads to an increase in the crack resistance, as well as the hardness of ceramics. The increase in strength properties can be explained by an increase in the dislocation density and the volume contribution of grain boundaries, which lead to hardening and an increase in resistance. During determination of the radiation damage resistance, it was found that a decrease in grain size to 50-70 nm leads to a decrease in the degree of radiation damage and the preservation of the resistance of irradiated ceramics to destruction and cracking.

Synthesis, Properties and Photocatalytic Activity of CaTiO3-Based Ceramics Doped with Lanthanum.

The aim of this work is to study the effect of lanthanum doping on the phase formation processes in ceramics based on CaTiO3, as well as to evaluate the effectiveness of the ceramics as photocatalysts for the decomposition of the organic dye Rhodamine B. The methods used were scanning electron microscopy to evaluate the morphological features of the synthesized ceramics, X-ray diffraction to determine the phase composition and structural parameters, and UV-Vis spectroscopy to determine the optical properties of the ceramics. During the experiments it was found that an increase in the lanthanum dopant concentration from 0.05 to 0.25 mol leads to the formation of the orthorhombic phase La0.3Ca0.7TiO3 and the displacement from the ceramic structure of the impurity phase TiO2, which presence is typical for the synthesized ceramics by solid-phase synthesis. On the basis of the data of the X-ray phase analysis the dynamics of phase transformations depending on concentration of lanthanum was established: CaTiO3/TiO2 → CaTiO3/La2TiO5 → CaTiO3/La0.3Ca0.7TiO3 → La0.3Ca0.7TiO3. During the determination of photocatalytic activity it was found that the formation of La0.3Ca0.7TiO3 phase leads to an increase in the decomposition rate as well as the degree of mineralization.

Study of Corrosion Mechanisms in Corrosive Media and Their Influence on the Absorption Capacity of Fe2O3/NdFeO3 Nanocomposites.

This paper presents the results of a study of the change in the stability of Fe2O3/NdFeO3 nanocomposites when exposed to aggressive media over a long period of time. The main purpose of these studies is to investigate the mechanisms of degradation and corrosion processes occurring in Fe2O3/NdFeO3 nanocomposites, as well as the influence of the phase composition on the properties and degradation resistance. According to the X-ray phase analysis, it was found that the variation of the initial components leads to the formation of mixed composition nanocomposites with different Fe2O3/NdFeO3 phase ratios. During corrosion tests, it was found that the dominance of the NdFeO3 phase in the composition of nanocomposites leads to a decrease in the degradation and amorphization rate of nanostructures by a factor of 1.5-2 compared to structures in which the Fe2O3 phase dominates. Such a difference in the degradation processes indicates the high stability of two-phase composites. Moreover, in the case of an aqueous medium, nanocomposites dominated by the NdFeO3 phase are practically not subjected to corrosion and deterioration of properties. The results obtained helped to determine the resistance of Fe2O3/NdFeO3 nanocomposites to degradation processes caused by exposure to aggressive media, as well as to determine the mechanisms of property changes in the process of degradation. The results of the study of the absorption capacity of Fe2O3/NdFeO3 nanocomposites in the case of the purification of aqueous media from manganese and arsenic showed that a change in the phase ratio in nanocomposites leads to an increase in the absorption efficiency of pollutants from aqueous media.

Study of Magnetic Properties of Fe100-xNix Nanostructures Using the Mössbauer Spectroscopy Method.

Hyperfine interactions of 57Fe nuclei in Fe100-xNix nanostructures synthesized in polymer ion-track membranes were studied by Mössbauer spectroscopy. The main part of obtained nanostructures was Fe100-xNix nanotubes with bcc structure for 0 ≤ x ≤ 40, and with fcc structure for 50 ≤ x ≤ 90. The length, outside diameter and wall thickness of nanotubes were 12 µm, 400 ± 10 nm and 120 ± 5 nm respectively. For the studied nanotubes a magnetic texture is observedalong their axis. The average value of the angle between the direction of the Fe atom magnetic moment and the nanotubes axis decreases with increasing of Ni concentration for nanotubes with bcc structure from ~50° to ~40°, and with fcc structure from ~55° to ~46°. The concentration dependences of the hyperfine parameters of nanotubes Mössbauer spectra are qualitatively consistent with the data for bulk polycrystalline samples. With Ni concentration increasing the average value of the hyperfine magnetic field increases from ~328 kOe to ~335 kOe for the bcc structure and drops to ~303 kOe in the transition to the fcc structure and then decreases to ~290 kOe at x = 90. Replacing the Fe atom with the Ni atom in the nearest environment of Fe atom within nanotubes with bcc structure lead to an increase in the hyperfine magnetic field by "6-9 kOe", and in tubes with fcc structure-to a decrease in the hyperfine magnetic field by "11-16 kOe". The changes of the quadrupole shift and hyperfine magnetic field are linearly correlated with the coefficient -(15 ± 5)·10-4 mm/s/kOe.