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At least 1,171 records · Page 65

Effect of Barothermal Processing on the Solid-State Formation of the Structure and Properties of 16 at % Si–Al Hypereutectic Alloy

We describe barothermal processing (hot isostatic pressing) of a 16 at % Si–Al binary alloy for 3 h at a temperature of 560°C and pressure of 100 MPa for 3 h, in combination with measurements of heat effects during cooling. The results demonstrate that this processing leads to the fragmentation of the silicon structural constituent and ensures a high degree of homogenization of the as-prepared alloy. Heat treatment of the 16 at % Si–Al alloy at 560°C and a pressure of 100 MPa leads to a thermodynamically driven enhanced silicon dissolution, up to ~10 at %, in the aluminum matrix, resulting in the formation of a supersaturated solid solution, which subsequently decomposes during cooling. We analyze the complete porosity elimination process, which makes it possible to obtain a material with 100% relative density. According to differential barothermal analysis, microstructural analysis, and scanning and transmission electron microscopy data, barothermal processing of the 16 at % Si–Al alloy produces a bimodal size distribution of the silicon phase constituent: microparticles 3.6 μm in average size and nanoparticles down to ~1 nm in diameter. The Al matrix has been shown to contain a high density of edge dislocations. Barothermal processing reduces the thermal expansion coefficient and microhardness of the hypereutectic alloy. We conclude that solid-state barothermal processing is an effective tool for completely eliminating microporosity from the 16 at % Si–Al alloy, reaching a high degree of homogenization, and controlling the microstructure of the alloy, in particular by producing high dislocation density in the aluminum matrix.

36 MATERIALS SCIENCE↗

Effect of Er{sub 2}O{sub 3} dopant on electrical and optical properties of potassium sodium niobate silicate glass-ceramics

Highlights: • The KNN–SiO{sub 2} doped Er{sub 2}O{sub 3} glass-ceramics was prepared by incorporation method. • High dielectric constant (458.41 at 100 kHz) and low loss (0.0005) could be obtained. • TEM and SEM confirmed the existence of KNN crystals embedded in glass matrix. • The Er{sub 2}O{sub 3} dopant causes insignificant effect on modifying E{sub g} value. - Abstract: In this study, transparent glass-ceramics from potassium sodium niobate (KNN)-silicate glass system doped with erbium oxide (Er{sub 2}O{sub 3}) were successfully prepared by incorporation method. KNN was added in glass batches as heterogeneous nucleating agent. The KNN powder was mixed with SiO{sub 2} and Er{sub 2}O{sub 3} dopant with KNN and Er{sub 2}O{sub 3} content varied between 70–80 and 0.5–1.0 mol%, respectively. Each batch was subsequently melted at 1300 °C for 15 min in a platinum crucible using an electric furnace. The quenched glasses were then subjected to heat treatment at various temperatures for 4 h. XRD results showed that the prepared glass ceramics contained crystals of KNN solid solution. In contrary, dielectric constant (ϵ{sub r}) and dielectric loss (tan δ) were found to increase with increasing heat treatment temperature. Additionally, optical properties such as absorbance and energy band gap have been investigated.

36 MATERIALS SCIENCE↗

Precipitation Kinetics in Binary Alloys near Grain Boundaries

Based on the method of the free energy density functional, the effect of grain boundaries on the precipitation process in binary alloys is considered. A comparative analysis of precipitation kinetics has been carried out for a single-crystal fragment of a solid solution and for a fragment containing a part of the boundary between two grains. We have found the influence of grain boundaries on the kinetics of the average radius of precipitates, their concentration, and nucleation rate for several compositions of the alloy.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Large-scale synthesis of Ba{sub x}Sr{sub 1−x}TiO{sub 3} nanowires with controlled stoichiometry

This study demonstrates a highly efficient method for large-scale synthesis BaTiO{sub 3} nanowires (NWs) using a two-step hydrothermal reaction. This synthesis process provides a facile approach to the growth of BaTiO{sub 3} NWs with high yield and control over the stoichiometry of the Ba{sub x}Sr{sub 1−x}TiO{sub 3} solid solution. The ferroelectricity of the BaTiO{sub 3} NWs is directly characterized using atomic force microscopy with the piezoelectric strain coupling coefficient (d{sub 33}) reaching 31.1 pm/V. This work provide an avenue for high volume manufacturing of ferroelectric NWs, allowing both fundamental investigation of nanoscale ferroelectricity as well as their future application in the electrical devices.

36 MATERIALS SCIENCE↗

Moderate active Fe 3+ doping enables improved cationic and anionic redox reactions for wide-voltage-range sodium storage

Layered metal oxides are promising cathode materials for sodium-ion batteries (SIBs) due to their high theoretical specific capacity and wide Na + diffusion channels. However, the irreversible phase transitions and cationic/anionic redoxes cause fast capacity decay. Herein, P2-type Na 0.67 Mg 0.1 Mn 0.8 Fe 0.1 O 2 (NMMF-1) cathode material with moderate active Fe 3+ doping has been designed for sodium storage. Uneven Mn 3+ /Mn 4+ distribution is observed in NMMF-1 and the introduction of Fe 3+ is beneficial for reducing the Mn 3+ contents both at the surface and in the bulk to alleviate the Jahn–Teller effect. The moderate Fe 3+ /Fe 4+ redox can realize the best tradeoff between capacity and cyclability. Therefore, the NMMF-1 demonstrates a high capacity (174.7 mAh g -1 at 20 mA g -1 ) and improved cyclability (78.5% over 100 cycles) in a wide-voltage range of 1.5–4.5 V (vs. Na + /Na). In-situ X-ray diffraction reveals a complete solid-solution reaction with a small volume change of 1.7% during charge/discharge processes and the charge compensation is disclosed in detail. This study will provide new insights into designing high-capacity and stable layered oxide cathode materials for SIBs.

25 ENERGY STORAGE↗

Wear Behavior of Vanadium and V-Ti-Ta Alloys under Reciprocating Sliding Conditions

Vanadium and newly developed V-Ti-Ta alloys have been systematically investigated for wear characteristics using ball-on-flat reciprocative sliding experiments. These materials have been tested at different sliding conditions (load and frequency) against hardened steel (AFBMA Grade 10) ball as counter-body. Coefficient of friction, wear volume and specific wear rate were measured and evaluated. Friction coefficient of vanadium and its alloys increases with increase in applied load irrespective of sliding frequencies. Wear rate decreases with increase in alloying content. Among the investigated compositions, V-4Ti-7Ta alloy exhibited superior wear performance having a least wear rate of 3.06 × 10{sup −6} mm{sup 3}/Nm, which is three times lower as compared with unalloyed vanadium when tested at 5 N and 5 Hz conditions. Addition of Ti and Ta strengthens the vanadium matrix by solid solution and contributes to enhanced wear resistance of the material without affecting the friction coefficient values. The major phases identified in the wear track regions were V{sub 2}O{sub 5} and Fe{sub 0.11}V{sub 2}O{sub 5.15}. Microstructural investigation reveals the predominant presence of adhesive wear regions at higher loads (15 N).

36 MATERIALS SCIENCE↗

The Mechanical and Microstructural Changes of Sn-Ag-Bi Solders with Cooling Rate and Bi Content Variations

The purpose of this study is to investigate the influence of cooling rate and Bi addition on the microstructure evolution and mechanical properties of Sn-3.5Ag alloy. A series of Sn-3.5Ag-xBi solders has been fabricated with Bi content in the range of 0.5-3.5 wt.%. After solution heat treatment at 170 °C for 24 h and subsequent aging heat treatment at 100 °C for 2 h, samples were divided into two groups. One group was rapidly quenched into iced water (water quenching) for the fast cooling rate (20 °C/s), while the second group was slowly cooled (furnace cooling) in the furnace for the slow cooling rate (0.2 °C/s) after the furnace reflow. The microstructural evolutions of the present solders have been investigated using x-ray diffraction and scanning electron microscopy. The microhardness was measured to correlate the mechanical properties to alloy compositions and cooling rate. It was found that the microhardness of Sn-3.5Ag-xBi solders increased with increasing cooling rate. The indentation creep curves have been evaluated from the obtained microhardness values. Results revealed the steady-state creep rate decreased with increasing Bi content exhibiting an anomalous behavior at 2.5Bi. The reason for improved creep resistance of Sn-3.5Ag-xBi solders is the result of the combination of the solid solution strengthening and precipitation strengthening of Bi. The mean values of stress exponent indicated that the operative creep mechanism is dislocation climb.

36 MATERIALS SCIENCE↗

The Influence of Segregation of Mn on the Recrystallization Behavior of C-Mn Steels

The influence of Mn segregation that occurs during casting on recrystallization kinetics has been explored for a C-Mn automotive steel. A homogenization heat treatment was used to remove Mn segregation, while maintaining a similar initial austenite grain size to the segregated condition, to provide base-line comparison data. Deformation trials were carried out in a Gleeble thermomechanical simulator to 0.3 strains at 900 °C, and significant differences in both recrystallization times and final grain sizes were seen between the two conditions. The segregated sample incurred a longer recrystallization time and a wider recrystallized grain size distribution than the homogenized sample. A finite element model was used to predict the local deformation strains based on variations in material properties caused by segregation; the model used data from XRF elemental mapping of Mn to define the local mechanical properties based on differences in solid solution strengthening. Local strain variations ranging from 0.19 to 0.49 were predicted in the segregated sample for an overall applied 0.3 strain (compared to 0.26 to 0.35 in the homogenized sample); using these strains to predict the recrystallized grain sizes gave a much better prediction for the grain size distribution.

36 MATERIALS SCIENCE↗

Effect of Heat Treatment on Microstructure and Mechanical Properties of Ti-6Al-4V-1.5Mn Fabricated by Powder Metallurgy

Ti-6Al-4V-1.5Mn alloy was prepared by powder metallurgy and solid solution aging treatment. Effect of composition segregation on properties of the titanium alloy was eliminated, and microstructure and the mechanical properties of the alloy were studied. Results show that the microstructure of Ti-6Al-4V-1.5Mn is composed of homogeneous α + β phase, and the optimal mechanical properties of the alloy are obtained when the solution temperature is 950 °C and the aging temperature is 460 °C. Analysis of the fracture illustrates that a small amount of dimple was found in the section and the fracture of the material was quasi-cleavage fracture.

36 MATERIALS SCIENCE↗

Microstructure and Mechanical Properties of a Ag Micro-Alloyed Mg-5Sn Alloy

Effects of 1.5 wt.% Ag addition and solid solution + artificial ageing at 160 °C on the microstructure and mechanical properties of a Mg-5Sn alloy have been studied. The results show that Ag addition has significantly hardened the solution-treated Mg-5Sn alloy. During the ageing process, the hardness increase rate and the strength and ductility of the Mg-5Sn alloy at each state are also improved by Ag addition. The improved strengthening behavior is primarily attributed to the refinement distribution of the Mg{sub 2}Sn precipitates, the enhanced precipitation process, and the synergistic strengthening effect of Mg{sub 2}Sn and a metastable plate DO{sub 19} phase formed at lower ageing temperature. For each solution-treated alloy, the strength and ductility are higher than the corresponding cast ones. Ageing further enhances the yield strength, and the ductility of the Mg-5Sn-1.5Ag alloy is also increased after ageing. The fracture surfaces of the both peak-aged alloys exhibit the characteristic of a mixture of quasi-cleavage and ductile fracture.

36 MATERIALS SCIENCE↗

Oxygen potential measurement and point defect chemistry of UO{sub 2}

Many studies on the oxygen potential of UO{sub 2} have been carried out so far. However, the oxygen potential data for UO{sub 2} near the stoichiometric composition in the high temperature region (1673-1873 K) are limited. Recently, Kato's group had investigated oxygen potential of (U, Pu)O{sub 2} as functions of Pu content, oxygen-to-metal (O/M) ratio and temperature. They evaluated the data based on defect chemistry. The UO{sub 2} data are fundamental to evaluate oxygen potential in UO{sub 2}-PuO{sub 2} solid solution. In this work, the oxygen potential data of UO{sub 2+x} were extended to the high temperature range of 1673-1873 K by gas equilibrium method. The measured data were analyzed based on a defect chemistry model. Kroeger-Vink's diagram were obtained in UO{sub 2+x}. (authors)

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Effect of Nano-Y{sub 2}O{sub 3} on Microstructure and Crack Formation in Laser Direct-Deposited In Situ Particle-Reinforced Fe-Based Coatings

In situ hard-particle-reinforced Fe-based composite coatings were prepared on Q235 steel substrates by direct laser deposition using Fe-based alloy powders containing 2 wt.% B, 3 wt.% Si and 1-3 wt.% nano-Y{sub 2}O{sub 3}. The microstructures, phase compositions, hardnesses and wear resistances of the deposited coatings with different nano-Y{sub 2}O{sub 3} contents were studied using metallographic microscopy, scanning electron microscopy, x-ray diffraction, transmission electron microscopy, microhardness tests and pin-on-disk abrasion tests (MMW-1A), respectively. The results showed that the appropriate addition of Y{sub 2}O{sub 3} played a role in grain refinement and in decreasing the number of brittle phases and impurity elements in the grain boundaries. Consequently, the number of cracks in the laser-deposited coating also decreased. The Fe-based composite coatings were mainly composed of α-Fe, γ-Fe and in situ-produced reinforced particle phases, such as Cr{sub 23}C{sub 6}, Cr{sub 7}C{sub 3}, (Cr, Fe){sub 7}C{sub 3}, Fe{sub 2}B, and CrFeB. When the content of nano-Y{sub 2}O{sub 3} was 2 wt.%, a Fe-based composite coating with a thickness of 4 mm that was free of cracks was obtained, and its surface hardness reached 650HV. Moreover, the wear resistance of the coating with 2 wt.% nano-Y{sub 2}O{sub 3} was the best among the samples studied. The presence of nano-Y{sub 2}O{sub 3} increased the solubility of Cr and Si in the solid solution, which eliminated the residual austenite region, and as a result, the phase transformation from γ-Fe to α-Fe was restrained and the transformation stress was also limited, thereby decreasing the probability of cracks in the coatings.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

MgCoAl and NiCoAl LDHs synthesized by the hydrothermal urea hydrolysis method: Structural characterization and thermal decomposition

Highlights: • We synthesized MgCoAl and NiCoAl LDHs by the urea hydrolysis method. • Aluminum rich and crystalline materials have been formed. • The calcination of the LDHs generated mixed oxides with high surface areas. - Abstract: Layered double hydroxides (LDHs) with Mg/Co/Al and Ni/Co/Al were synthesized for the first time by the urea hydrolysis method. The experimental conditions promoted aluminum rich and crystalline materials. The formation of LDHs was investigated by powder X-ray diffraction (XRD), chemical analysis, solid state nuclear magnetic resonance with magic angle spinning ({sup 27}Al-MAS-NMR), simultaneous thermogravimetric/differential thermal analysis (TGA/DTA), FTIR spectroscopy, scanning electron microscopy (SEM), and N{sub 2} adsorption–desorption experiments. A single phase corresponding to LDH could be obtained in all the investigated compositions. Thermal calcination of these LDHs at 500 °C resulted in the formation of solid solutions in which Al{sup 3+} was dissolved. All the calcined materials have rock-salt like structures and high surface areas.

36 MATERIALS SCIENCE↗

Radiation damage buildup by athermal defect reactions in nickel and concentrated nickel alloys

We develop a new method using binary collision approximation simulating the Rutherford backscattering spectrometry in channeling conditions (RBS/C) from molecular dynamics atom coordinates of irradiated cells. The approach allows comparing experimental and simulated RBS/C signals as a function of depth without fitting parameters. The simulated RBS/C spectra of irradiated Ni and concentrated solid solution alloys (CSAs, NiFe and NiCoCr) show a good agreement with the experimental results. The good agreement indicates the damage evolution under damage overlap conditions in Ni and CSAs at room temperature is dominated by defect recombination and migration induced by irradiation rather than activated thermally.

36 MATERIALS SCIENCE↗

Thermal Expansion of EuF{sub 2+x} Single Crystals and Their Thermal Stability

Thermal expansion of an EuF{sub 2.136} nonstoichiometric crystal with the fluorite structure type (Eu{sub 0.864}{sup 2+}Eu{sub 0.136}{sup 3+}F{sub 2.136}, lattice parameter 5.82171(5) Å) has been experimentally investigated in the temperature range of 9–500 K. The coefficient of thermal expansion is α = 15.8 × 10{sup –6} K{sup –1} at T = 300 K. The observed anomalies in the behavior of the coefficient of thermal expansion at T > 400 K are related to the oxidation processes with partition of Eu{sup 2+} ions. It is established by differential scanning calorimetry that the onset temperature of EuF{sub 2+x} oxidation in air is 430 K and that this process occurs in three stages. X-ray diffraction analysis shows that the oxidation is accompanied by the formation of a phase mixture based on two modifications of the Eu{sub 1–y}{sup 3+}Eu{sub y}{sup 2+}F{sub 3–y} solid solution with the structure types of tysonite (LaF{sub 3}), orthorhombic β-YF{sub 3} phase, and europium oxyfluorides of variable composition EuO{sub 1–x}F{sub 1+2x}, with dominance of the latter.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Microstructural Characteristics and Mechanical Properties of an Electron Beam-Welded Ti/Cu/Ni Joint

Electron beam welding experiments of TA15 titanium alloy to GH600 nickel superalloy with and without a copper sheet interlayer were carried out. Surface appearance, microstructure and phase constitution of the joint were examined by optical microscopy, scanning electron microscopy and x-ray diffraction analysis. Mechanical properties of Ti/Ni and Ti/Cu/Ni joint were evaluated based on tensile strength and microhardness tests. The results showed that cracking occurred in Ti/Ni electron beam weldment for the formation of brittle Ni-Ti intermetallics, while a crack-free electron beam-welded Ti/Ni joint can be obtained by using a copper sheet as filler metal. The addition of copper into the weld affected the welding metallurgical process of the electron beam-welded Ti/Ni joint significantly and was helpful for restraining the formation of Ti-Ni intermetallics in Ti/Ni joint. The microstructure of the weld was mainly characterized by a copper-based solid solution and Ti-Cu interfacial intermetallic compounds. Ti-Ni intermetallic compounds were almost entirely suppressed. The hardness of the weld zone was significantly lower than that of Ti/Ni joint, and the tensile strength of the joint can be up to 282 MPa.

36 MATERIALS SCIENCE↗

Ionic conductivity and the formation of cubic CaH{sub 2} in the LiBH{sub 4}–Ca(BH{sub 4}){sub 2} composite

LiBH{sub 4}–Ca(BH{sub 4}){sub 2} composites were prepared by ball milling. Their crystal structures and phase composition were investigated using synchrotron X-ray diffraction and Rietveld refinement, and their ionic conductivity was measured using impedance spectroscopy. The materials were found to form a physical mixture. The composites were composed of α-Ca(BH{sub 4}){sub 2}, γ-Ca(BH{sub 4}){sub 2} and orthorhombic LiBH{sub 4}, and the relative phase quantities of the Ca(BH{sub 4}){sub 2} polymorphs varied significantly with LiBH{sub 4} content. The formation of small amounts of orthorhombic CaH{sub 2} and cubic CaH{sub 2} in a CaF{sub 2}-like structure was observed upon heat treatment. Concurrent formation of elemental boron may also occur. The ionic conductivity of the composites was measured using impedance spectroscopy, and was found to be lower than that of ball milled LiBH{sub 4}. Electronic band structure calculations indicate that cubic CaH{sub 2} with hydrogen defects is electronically conducting. Its formation along with the possible precipitation of boron therefore has an effect on the measured conductivity of the LiBH{sub 4}–Ca(BH{sub 4}){sub 2} composites and may increase the risk of an internal short-circuit in the cells. -- Graphical abstract: An Arrhenius plot of the ionic conductivity of the LiBH{sub 4}–Ca(BH{sub 4}){sub 2} composites (red, blue, green). The ionic conductivity of ball milled (gray) and non-milled (black) LiBH{sub 4} is shown for comparison. The filled symbols are measured during heating runs and the empty symbols are measured during subsequent cooling runs. The conductivity of the composites is in all cases higher during cooling, most probably due to the formation of an electronically conducting layer containing defect-rich cubic CaH{sub 2}. Such layer formation could eventually lead to a short circuit in the cell and reveals a general issue of chemical stability that should be attended to in the development of solid electrolyte materials. Highlights: • The LiBH{sub 4}–Ca(BH{sub 4}){sub 2} composite forms a physical mixture rather than a solid solution. • The formation of defect-rich, cubic CaH{sub 2} in a CaF{sub 2}-like structure is observed. • A new layer containing cubic CaH{sub 2} is conducting and may lead to a short-circuit.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

A study of defects in iron-based binary alloys by the Mössbauer and positron annihilation spectroscopies

The room temperature positron annihilation lifetime spectra and {sup 57}Fe Mössbauer spectra were measured for pure Fe as well as for iron-based Fe{sub 1−x}Re{sub x}, Fe{sub 1−x}Os{sub x}, Fe{sub 1−x}Mo{sub x}, and Fe{sub 1−x}Cr{sub x} solid solutions, where x is in the range between 0.01 and 0.05. The measurements were performed in order to check if the known from the literature, theoretical calculations on the interactions between vacancies and solute atoms in iron can be supported by the experimental data. The vacancies were created during formation and further mechanical processing of the iron systems under consideration so the spectra mentioned above were collected at least twice for each studied sample synthesized in an arc furnace— after cold rolling to the thickness of about 40 μm as well as after subsequent annealing at 1270 K for 2 h. It was found that only in Fe and the Fe-Cr system the isolated vacancies thermally generated at high temperatures are not observed at the room temperature and cold rolling of the materials leads to creation of another type of vacancies which were associated with edge dislocations. In the case of other cold-rolled systems, positrons detect vacancies of two types mentioned above and Mössbauer nuclei “see” the vacancies mainly in the vicinity of non-iron atoms. This speaks in favour of the suggestion that in iron matrix the solute atoms of Os, Re, and Mo interact attractively with vacancies as it is predicted by theoretical computations and the energy of the interaction is large enough for existing the pairs vacancy-solute atom at the room temperature. On the other hand, the corresponding interaction for Cr atoms is either repulsive or attractive but smaller than that for Os, Re, and Mo atoms. The latter is in agreement with the theoretical calculations.

36 MATERIALS SCIENCE↗