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Zirconium (Zr) is an important industrial metal that is widely used in nuclear engineering, chemical engineering, and space and aeronautic engineering because of its unique properties. The high-pressure behaviors of Zr have been widely investigated in the past several decades. However, the controversies still remain in terms of the phase transition (PT) pressures and the isostructural PT in β-Zr: why the PT pressure in Zr is so scattered, and whether the β to β’ PT exists. In the present study, to address these two issues, the Zr sample with ultra-high purity (>99.99%) was quasi-hydrostatically compressed up to ~70 GPa. We discovered that both the purity and the stress state of the sample (the grade of hydrostaticity/nonhydrosaticity) affect the PT pressure of Zr, while the stress state is the dominant factor, the nonhydrostaticity significantly promotes the PT of Zr. We also propose two reasons why the β-β’ isostructural PT was absent in the subsequent and present experiments, which call for further investigation of Zr under quasi-compression up to 200 GPa or even higher pressures.

The first results are presented for U-Pb SHRIMP-II dating of zircons from the upper part of the Khivachian regional horizon (stage) of the Regional Stratigraphic Scale (RSS) of the Permian in northeastern Russia. The obtained isotope age of 255 [+ or -] 2 Ma is close to that of the present boundary between the Wuchiapingian and Changhsingian stages of the Permian system in the International Stratigraphic Scale (254.1 Ma). Based on the distribution of bivalves--Intomodesma spp. and Claraioides aff.primitivus (Yin)--in the sections considered, their relations to the stratigraphic positions of the samples considered and dated formerly, and in view of the interregional correlation of recent [[delta].sup.13][C.sub.org] data for clayey rocks, one may assume with certainty that most of the regional zone of Intomodesma costatum corresponds to the upper part of the Wuchiapingian stage. Here, the Changhsingian stage in northeastern Asia complies only with the uppermost part of this zone within the I. postevenicum subzone and, partially, of Otoceras layers within the Otoceras concavum zone.

Nitride film as a hydrogen permeation barrier on zirconium hydride has seldom been studied. In this work, the zirconium nitride films were prepared on zirconium hydride in an atmosphere of N2 and N2 + H2 at 500~800 °C, with a holding time of 5 h and 20 h, and the mechanisms of film growth and hydrogen permeation were analyzed. The results showed that the film growth was mostly influenced by the temperature, followed by the reaction atmosphere and the holding time. The hydrogen could increase the nitrogen diffusivity during the formation of zirconium nitride films. The in situ nitriding conditions were optimized as 800 °C, N2 + H2 atmosphere, and 5~20 h. The chemical composition of ZrN-based films was mainly comprised of Zr and N, with a minor content of O. In addition, the film exhibited a major phase of ZrN, accompanied by the coexistence of ZrO2, ZrO, ZrN(NH2), and ZrN0.36H0.8, as well as O-H and N-H bonds based on the XPS analysis. The as-prepared ZrN base films in the present study exhibited superior hydrogen permeation resistance to other ZrO2 films previously reported. The hydrogen permeation resistance of the films could be attributed to the following mechanisms, including the chemical capture of hydrogen by the above-mentioned compounds and bonds; the physical barrier of continuous and dense film incurred from the volume effect of different compounds based on Pilling–Bedworth model and the different nitrogen diffusion coefficients at different temperatures.

During the hot dip aluminum plating process, components such as sinking rollers, pulling rollers, and guide plates will come into long-term contact with high-temperature liquid aluminum and be corroded by the aluminum liquid, greatly reducing their service life. Therefore, the development of a material with excellent corrosion resistance to molten aluminum is used to prepare parts for the dipping and plating equipment and protect the equipment from erosion, which can effectively improve the production efficiency of the factory and strengthen the quality of aluminum-plated materials, which is of great significance for the growth of corporate profits. With AlFeNiCoCr as the binder phase and ZrB[sub.2] as the hard phase, ZrB[sub.2]-based ceramic composites were prepared by spark plasma sintering (SPS). SEM, EDS and XRD were used to characterize the microstructure and properties of the sintered, corroded, and abraded material samples. The density, fracture toughness, corrosion rate and wear amount of the composite material were measured. The results show that ZrB[sub.2]-AlFeNiCoCr ceramics have compact structure and excellent mechanical properties, and the density, hardness and fracture toughness of ZrB[sub.2]-AlFeNiCoCr increase with the increase in sintering temperature. However, when the composite material is at 1600 °C, the relative density of the sintering at 1600 °C decreases due to the overflow of the bonding phase. Therefore, when the sintering temperature is 1500 °C, the high entropy alloy has the best performance. The average corrosion rate of ZrB[sub.2]-1500 at 700 °C liquid aluminum is 1.225 × 10[sup.−3] mm/h, and the wear amount in the friction and wear test is 0.104 mm[sup.3].

Hydrogen permeation barrier plays an important role in reducing hydrogen loss from zirconium hydride matrix when used as neutron moderator. Here, a composite nitride film was prepared on zirconium hydride by in situ reaction method in nitrogen atmosphere. The phase structure, morphology, element distribution, and valence states of the composite film were investigated by XRD, SEM, AES, and XPS analysis. It was found that the composite nitride film was continuous and dense with about 1.6 μm thickness; the major phase of the film was ZrN, with coexistence of ZrO2, ZrO, and ZrN0.36H0.8; and Zr-C, Zr-O, Zr-N, O-H, and N-H bonds were detected in the film. The existence of ZrN0.36H0.8 phase and the bonds of O-H and N-H revealed that the nitrogen and oxygen in the film could capture hydrogen from the zirconium hydride matrix. The hydrogen permeation performance of nitride film was compared with oxide film by permeation reduction factor (PRF), vacuum thermal dehydrogenation (VTD), and hydrogen permeation rate (HPR) methods, and the results showed that the hydrogen permeation barrier effects of nitride film were better than that of oxide film. The zirconium nitride film would be a potential candidate for hydrogen permeation barrier on the surface of zirconium hydride.

Polymethyl methacrylate (PMMA) is widely used for the fabrication of removable prostheses. Recently, zirconium oxide nanoparticles (nano-ZrO ) have been added to improve some properties of PMMA, but their effect on the optical properties and tensile strength are neglected. The aim of this study was to investigate the effect of nano-ZrO addition on the translucency and tensile strength of the PMMA denture base material. Eighty specimens (40 dumbbell-shaped and 40 discs) were prepared out of heat-polymerized acrylic resin and divided into four groups per test (n=10). The control group for each test included unreinforced acrylic, while the test groups were reinforced with 2.5, 5, and 7.5 wt% nano-ZrO . Acrylic resin was mixed according to manufacturer's instructions, packed, and processed by conventional method. After polymerization, all specimens were finished, polished, and stored in distilled water at 37°C for 48±2 hours. Tensile strength (MPa) was evaluated using the universal testing machine while the specimens' translucency was examined using a spectrophotometer. Statistical analysis was carried out by SPSS using the paired sample -test ( ≤0.05). A scanning electron microscope was used to analyze the morphological changes and topography of the fractured surfaces. This study showed that the mean tensile strength of the PMMA in the test groups of 2.5%NZ, 5%NZ, and 7.5%NZ was significantly higher than the control group. The tensile strength increased significantly after nano-ZrO addition, and the maximum increase seen was in the 7.5%NZ group. The translucency values of the experimental groups were significantly lower than those of the control group. Within the reinforced groups, the 2.5%NZ group had significantly higher translucency values when compared to the 5%NZ and 7.5%NZ groups. The addition of nano-ZrO increased the tensile strength of the denture base acrylic. The increase was directly proportional to the nano-ZrO concentration. The translucency of the PMMA was reduced as the nano-ZrO increased. Based on the results of the current study, the tensile strength was improved with different percentages of nano-ZrO additions. However, translucency was adversely affected. Therefore, it is important to determine the appropriate amount of reinforcing nano-ZrO that will create a balance between achieved properties - mechanical and optical.

In this study suitability of [alpha]-ZrP nanoparticles as a .sup.223Ra and .sup.225Ac carriers for TAT was investigated. The yields of radiolabelling were higher than 98% in both cases. Subsequently, in vitro stability studies were carried out in various biological matrices during 48 h period. Measurements of released radioactivity showed the highest stability in saline. Released activity of .sup.223Ra, .sup.225Ac and their daughter radionuclides was around 0.5%. On the other hand, the lowest stability was shown in plasma and serum. Released activity for .sup.223Ra, .sup.225Ac and their progeny atoms was from 15 to 32%.

The interest for ZrP this material is based on its physicochemical properties which makes this material a perspective candidate for applications in nuclear medicine. In this study ZrP was prepared and completely characterized using various analytical methods. Finally, the study of radiometals sorption mechanism on a surface of ZrP and the surface characterization of ZrP were done. In conclusion, ZrP appears as promising for next studies with various purposes like drug delivery system or ion-exchanger for separations of medical radionuclides such as .sup.225Ac and .sup.213Bi.