Papers by Keyword: Solid Solution

Abstract: The aim of the paper is to define the limits of substitution and phase stability for solidsolutions of orthovanadates with zircon structure Sc1–xLnxVO4, where Ln is a rare-earth element(REE), Ln = Ce – Lu. The mixing energies (interaction parameters) and critical decompositiontemperatures of Sc1–xLnxVO4 solid solutions with the zircon structure were calculated using thecrystal-energy theory of isomorphous miscibility. Diagram of thermodynamic stability visualizingthe substitution limits (x) by the decomposition temperature or the decomposition temperature bythe substitution limits, the dependencies of the decomposition temperatures on the REE atomicnumbers is presented. This diagram also allows assessing areas of stability, instability, andmetastability for Sc1–xLnxVO4 solid solutions. Results of calculations were compared with literaturedata on thermodynamic stability of solid solutions and on substitution limits. The results of thisstudy can be used in the development of new luminescent materials based on ScVO4 modified withREE, in the selection of REE for matrix and activator, in defining optimal proportions of REE inSc1–xLnxVO4 matrices.

Abstract: The oxidation behaviors of tantalum-tungsten alloy with 10-20% W was investigated between temperature range of 700 to 900 °C exposed in air. The kinetics of Ta-W alloy was determined by TG-DTA, the characteristics of oxides were analyzed by SEM, EDS and XRD. The oxidation tests revealed that the alloys obeyed parabolic kinetic in the initial stage, then translated in linear law. The addition of W has a good effect on the oxidation resistance of Ta-W alloys at experimental temperature. Solid solution of Ta₂O₅ form in case of oxidation product of Ta-10W, Ta-15W alloys, while the complex oxide Ta₂₂W₄O₆₇ form after Ta-20W alloy oxidized. The formation of solid solution and complex oxide impeded the volatilization. The compact oxide film protects the penetration of oxygen in the initial oxidation stage. The large compressive stresses and mismatch of the coefficient of thermal expansion between oxide scale and matrix alloys make the oxides layer be broken, which cause kinetic of oxidization obeying linear law.

Abstract: Chromium aluminum nitride (CrAlN) has been extensively studied because of high hardness, high oxidation and corrosion resistance, and good wear resistance. However, utilizing substrate treatments such as heating and voltage biasing during film deposition usually leads to relatively high surface roughness that affects wear rates. It has been found that sputter deposition at low substrate temperatures can produce nano-grain coatings with enhanced structure and mechanical properties. For this reason, the CrAlN in this study was prepared by a reactive co-sputtering technique without the substrate treatments. Effects of Al content on structure and mechanical properties were investigated by X-ray diffraction, field-emission scanning electron microscopy, energy-dispersive X-ray spectrometry, atomic force microscopy, X-ray photoelectron spectroscopy, and nanoindentation. The results suggest that these CrAlN films formed as solid solutions by substitution of Al for Cr in the CrN crystalline structure. The deposition with increasing Al but fixed N leads to N deficiency, therefore at high Al content these films form under 1:1 stoichiometric nitride. This lowers film crystallinity and hence refined film morphology. Surface roughness and hardness of the films decreased from 5.737 to 1.135 nm and from 31.69 to 26.56 GPa, respectively. However, the solid solution strengthening arising from the further increase of the Al content causes these values to rebound to 2.466 nm and to 30.16 GPa.

Abstract: The ZrW_2-xMo_xO₈ (0≤x≤2) system has a unique property - a negative coefficient of thermal expansion (CTE), that is it shrinks when heated. Such materials solve the problem of undesirable thermal expansion of composites in many areas. In contradistinction to ZrW₂O₈ and ZrMo₂O₈, this system has anomalously low CTE values [1,2] and adverse phase transition is shifted to a lower temperature, unlikely area for operation [3,4]. At the same time, the fundamental question remains about the mechanism of formation of ZrW_2-xMo_xO₈(0≤x≤2). According to [5,6], pure cubic ZrW₂O₈ and ZrMo₂O₈ are obtained by thermal decomposition of the precursor ZrM₂O₇(OH)₂· 2H₂O, where (M = Mo, W). However, the structure of the precursor is extremely sensitive to various changes in the synthesis process. To date, there are a number of works devoted to the hydrothermal synthesis of precursors ZrW_2-xMo_xO₇(OH)₂·2H₂O (0≤x≤2) solid solutions, however, not all formulations were obtained during the hydrothermal reaction. The study of their thermal properties, as well as structural and phase transformations are not fully studied. Within the paper it was first time proposed to obtain full number of nanosized materials by the hydrothermal method and also to study the nature of the thermal expansion of each member of the solid solution. The obtained data will solve many technical problems associated with dimensional nonvariance in the electronic, oil and gas, optical industry, medicine and rocket engineering.

Abstract: Very thin titanium chromium nitride (TiCrN) films with various Ti content were deposited by unbalanced magnetron co-sputtering of Ti and Cr metals. Deposition time was set to 15 min to achieve film thickness ranging from 142 to 190 nm. Silicon wafers and copper grids were used as substrates. The Ti current (I_Ti) was varied from 0.4 to 1.0 A to achieve the differnt Ti content whereas Cr current (I_Cr) was fixed to 0.6 A. Effects of the Ti content on structure and morphology of these TiCrN thin films were studied by X-ray diffraction (XRD), transmission electron microscopy (TEM), atomic force microscopy (AFM), field emission scanning electron microscopy (FE-SEM), and energy-dispersive X-ray spectroscopy (EDS). The XRD revealed that the films showed crystalline structure with fcc phase and were formed as Ti_xCr_1-xN solid solution with a crystallite size of about 13 nm. The TEM result confirmed that the films were polycrystalline. The AFM images of the films showed dome top characteristic with root-mean-square roughness slightly decreasing from 1.643 to 1.273 nm. FE-SEM cross-sectional images exhibited development of film morphology from columnar structure corresponding to zone 1 of Thornton’s structure zone model to fine structure gradually with the increase of the Ti content.

Abstract: The phase equilibria in the ternary systems {Ce, Gd}–{Ti, Zr}–Sb were investigated by means of X-ray powder diffraction and energy-dispersive X-ray spectroscopy. The isothermal sections of the phase diagrams at 600°C were constructed. The formation of three ternary compounds (Ce₂Ti₇Sb₁₂, Ce₃TiSb₅, and Gd₂Ti₁₁Sb₁₄) was confirmed in the {Ce, Gd}–Ti–Sb systems and no more ternaries were found. The investigation of the {Ce, Gd}–Zr–Sb systems revealed several new ternary compounds and confirmed the known ones. The crystal structure of the new compound Ce_0.08(3)Zr_1.92(3)Sb was determined from X-ray powder diffraction data. The other new compounds in the Ce–Zr–Sb system were found to have compositions close to ~CeZrSb₄ and ~Ce₂Zr₃Sb₅. In the Gd–Zr–Sb system the existence of a large homogeneity range was established for the GdZrSb compound along the isoconcentrate 33.3 at.% Sb: Gd_1-xZr_1+xSb (x = 00.905(18) at 600°C), and a new compound, ~Gd₃Zr₃Sb₁₄, was discovered. The crystal structures at the boundary compositions of the Gd_1-xZr_1+xSb phase were refined from X-ray powder diffraction data.

Abstract: The macroscopic strain rate sensitivity m and apparent activation energy Q are derived from their microscopic counterparts associated with strain hardening, grain boundary mobility, and nucleation rate in the case of steady state discontinuous dynamic recrystallization (DDRX). The case of solid solutions, involving effects of the solute concentration on strain hardening and boundary mobility, is also taken into consideration. Moreover, three distinct Derby exponents are introduced to refine the correlation between steady state flow stress and average grain size. Hot torsion data and micrographic observations on a set of nickel-niobium alloys are used to assess the predictions of this tentative approach.

Abstract: Different molar ratio of HfB₂ and ZrB₂ had been mixed, and 30 vol.% SiC was selected as sintering additives. The mixing powders were sintered by hot pressing at 1900 °C for 1 h under a pressure of 20 MPa in Ar atmosphere. X-ray diffraction, scanning microscopy and Archimedes’s method were used to characterize the phase, microstructure and density of the sintered composites. Meanwhile, the hardness, the fracture toughness and flexural strength of the obtained composites were considered too. It can be found that the (Zr,Hf)B₂ solid solutions were formed by HfB₂ and ZrB₂ during the sintering. The flexural strength of (Zr,Hf)B₂-SiC composites increased with the amount of HfB₂ increasing, which reached (332±40) MPa for the composites content of 70% HfB₂. Which fracture toughness was (2.22±0.25) MPa·m^1/2. The highest Vickers’ harness of was (24.8±3.4) GPa for the composites content of 50% HfB₂.

Abstract: Mechanical alloying (MA) is a simple and versatile dry powder processing technique that has been used for the manufacture of both equilibrium and metastable phases of commercially useful and scientifically interesting materials. It owes its origin to an industry need to develop a nickel-based super alloy for gas turbine applications that had both oxide dispersion strengthening and precipitation hardening. This far-from equilibrium powder metallurgy processing technique involves fracturing, welding and re-welding of powder particles in a High Energy Ball Mill (HEBM). MA is an economically viable process with important technical advantages. Its utmost advantage is in the synthesis of novel alloys, e.g., alloying of ordinarily immiscible elements, that is not possible by any other technique. As MA is a completely solid-state processing technique, the limitations imposed by phase diagrams do not apply to it. The MA process is capable of producing different types of metastable effects in a variety of alloy systems. Some of the metastable effects achieved by MA are solid solution formation and amorphisation. MA has the possibility of producing superior and enhanced materials than those produces by conventional methods. In this work a review of MA and its present and potential applications for Ti-based materials are presented.

Abstract: Mechanical alloying (MA) is a high-energy ball milling process results in the obtaining of simple and stable microstructures having increased homogeneity compared to other non-equilibrium synthesis methods. The aim of this paper was to develop a high entropy alloy with an improved hardness value suitable for coating turbine blades working in geothermal steam. CoCrFeNiMo high entropy alloy was processed in solid state, using mechanical alloying. After 40h milling time in a planetary ball mill the alloyed sample was consolidated using spark plasma sintering process. The samples obtained were investigated with the aid of optical and electron microscope, X ray diffraction and the hardness value was determined. The results obtained revealed that the powder was completely alloyed after 40 hour milling and the mixture between BCC and FCC phases resulted in 34% improved hardness value in comparison with a stainless steel usually used for turbine blades working in geothermal environment.