Increasing Sintering Temperature Research Articles

Effect of sintering temperature on microstructure and mechanical properties of MoNbVTa0.5Cr high-entropy alloys fabricated by powder metallurgy method

To address the challenges posed by the high density and low plasticity at room temperature of traditional refractory high entropy alloys (RHEAs), the MoNbVTa0.5Cr RHEA was synthesized through a combination of mechanical alloying (MA) and spark plasma sintering (SPS) techniques. The effects of different sintering temperatures on the microstructure and mechanical properties of the alloy were systematically studied. The MoNbVTa0.5Cr RHEA milled up to 60 h was found to have a metastable dual-phase containing a major BCC (a = 3.1474 Å) and Nb-Ta (a = 3.3058 Å) phase. The sintered MoNbVTa0.5Cr RHEA was composed of BCC phase and a small amount of Ta2VO6 at different sintering temperatures. There were a lot of edge dislocations in the BCC matrix near the BCC/Ta2VO6 interface. With the increase of sintering temperature, the grain size of sintered MoNbVTa0.5Cr RHEA gradually increased, while the mechanical properties gradually decreased with the increase of sintering temperature. When the sintering temperature was 1500 °C, the grain size of the alloy was 2.33 μm, the yield strength was 2783 MPa, the compressive strength was 3346 MPa, and the fracture strain was 20.45 %, showing the best comprehensive properties. And the density of MoNbVTa0.5Cr RHEA was 9.11 g·cm−3 and 26 % lower than that of WNbMoTaV RHEA. The specific yield strength of MoNbVTa0.5Cr RHEA prepared in this research was 295.28 kPa·m3·kg−1, which was superior to most RHEAs reported so far. This sintered MoNbVTa0.5Cr RHEA showed an excellent room temperature compression performance, which can be attributed to the co-existence of BCC phase along with the minor Ta2VO6 phases. The high yield strength of MoNbVTa0.5Cr RHEA was mainly attributed to the substitutional solid solution strengthening of metal atoms, the interstitial solid solution strengthening of O atoms and the grain boundary strengthening of ultrafine grains, with contributions to yield strength of 41 %, 28 %, and 24 %, respectively.

Microstructural evolution in polycrystals with faceted boundaries

Various types of grain growth behavior have been observed in polycrystals with faceted boundaries. The grain growth behavior observed in many different ceramic as well as metallic systems has been well explained by the mixed mechanism principle of grain growth and microstructural evolution. However, relatively few studies have considered repetitive grain growth in materials. To examine the generality of the microstructural evolution principle, two cases of repetitive grain growth during solid-state sintering are considered, one metallic (Ni) and one ceramic system (BaTiO3). The observed repetitive grain growth behavior with an increased sintering temperature (in the case of Ni) and sintering time (in the case of BaTiO3) supports well the generality of the mixed mechanism principle.

Utilization of fused deposition modeling in the fabrication of lattice structural Al2O3 ceramics

This study focuses on fabricating lattice structural Al2O3 ceramics with lattice infill densities ranging from 25 % to 70 % using filament-based fused deposition modeling (FDM) technology. A specialized filament for FDM printing was developed, comprising 53 vol% Al2O3 powder and ethylene vinyl acetate (EVA) as the primary binder component. The filament demonstrated excellent flexibility as assessed by a self-designed three-point bending test. The impact of lattice infill density and sintering temperature on dimensional changes, microstructure evolution, compressive strength, and strength-to-density ratio was explored. It was found that with increasing sintering temperature, the samples became more compact, resulting in higher levels of shrinkage, bulk density, and compressive strength. At a sintering temperature of 1600 °C, the sintered parts reached their maximum density through the solid-state sintering process. The sample sintered at 1600 °C with 70 % infill density exhibited the maximum compressive strength of 31.47 MPa, with a corresponding strength-to-density ratio of 20.84 MPa/g·cm−3. These findings highlight the successful fabrication of lattice structural Al2O3 with low density and high compressive strength by FDM technology.

Microstructure and properties of tungsten‐40 wt.–% copper composites fabricated by binder jet 3D printing

AbstractIn this work, the tungsten‐copper composites were fabricated by binder jet 3D printing technology. The effects of different printing layer thicknesses (50 μm to 100 μm) on the green density and green strength were investigated. Then, under the optimal layer thickness, the effects of different sintering temperatures (1300 °C to 1600 °C) on the microstructure and densification of tungsten‐40 wt.–% copper composites were studied. The experimental results showed that when the printing layer thickness was set as a lower value (50 μm), the tungsten‐40 wt.–% copper green part had the best strength and its density reached a maximum value of 60.73 %. After sintering for green parts printed with 50 μm layer thickness, the relative density, thermal conductivity and electrical conductivity of sintered parts first increased and then decreased with increasing sintering temperature. In our experiments, the tungsten‐40 wt.–% copper sample fabricated by binder jet 3D printing with a printing layer thickness of 50 μm under a sintering temperature of 1500 °C displayed the best properties, in which the relative density, thermal conductivity and electrical conductivity were 97.04 %, 228 W⋅m−1⋅K−1 and 46.5 % IACS, respectively.

Characterization of LiNi0.8Co0.15Al0.05O2 cathode material synthesized via co-precipitation method

Abstract LiNi0.8Co0.15Al0.05O2 cathode material was synthesized using the co-precipitation method, and the effect of synthesis conditions on powder properties was studied. The results indicate that adjusting the pH value and complexing agent concentration during the reaction process can effectively control the precipitation process. The obtained hydroxide precursor is petallike, and the morphology of the cathode material powder after high-temperature sintering is well-dispersed spherical particles. The changes in the sintering system can significantly affect the crystallization process and crystal structure of cathode materials. As the sintering temperature increases, the peak rate I (003)/I (104) significantly decreases, while the R value increases. With the prolongation of sintering time, I (003)/I (104) first increases and then decreases, and the R value first decreases and then increases. After sintering at 750°C × 12 h, the cathode material has the highest peak rate and the lowest R value, indicating the lowest degree of cation mixing, higher structural integrity and the highest electrochemical activity at this time.

Elucidating the mechanical-electrochemical interactions in single crystalline LiNi0.7Co0.1Mn0.2O2 cathode material during solid-state calcination

In recent years, the shift towards single-crystalline Ni-rich LiNixCoyMn1-x-yO2 (NCM) cathode materials has intensified the focus on temperature regulation via the solid-state method, aiming to enhance electrochemical capacity and control crystal size. This study investigates how variations in crystal size, indicative of distinct lattice structures, affect lithium ion transport during the electrochemical charging/discharging cycle. Our findings reveal mechanical degradation in NCM samples correlating with increased sintering temperatures of LiOH·H2O and NCMOH precursors, as evidenced by nanoindentation tests measuring elastic modulus and hardness. Elevated sintering temperatures were observed to facilitate nucleation and crystal growth, albeit introducing oxygen vacancies potentially detrimental to the initial Coulombic Efficiency within the NCM lattice. This degradation in both mechanical and electrochemical properties underscores the critical impact of sintering temperature on structural integrity. Our systematic analysis provides essential insights into the interplay between structural characteristics and electrochemical performance, offering compelling evidence for the optimization of sintering temperatures in the preparation of NCM cathode materials.

The Microstructure, Mechanical, and Friction-Wear Properties of Boron Carbide-Based Composites with TiB2 and SiC Formed In Situ by Reactive Spark Plasma Sintering.

The paper presents the influence of the temperature of the sintering process on the microstructure and selected properties of boron carbide/TiB2/SiC composites obtained in situ by spark plasma sintering (SPS). The homogeneous mixture of boron carbide and 5% vol. Ti5Si3 micropowders were used as the initial material. Spark plasma sintering was conducted at 1700 °C, 1800 °C, and 1900 °C for 10 min after the initial pressing at 35 MPa. The heating and cooling rate was 200 °C/min. The obtained boron carbide composites were subjected to density measurement, an analysis of the chemical and phase composition, microstructure examination, and dry friction-wear tests in ball-on-disc geometry using WC as a counterpart material. The phase compositions of the produced composites differed from the composition of the initial powder mixture. Instead of titanium silicide, two new phases appeared: TiB2 and SiC. The complete disappearance of Ti5Si3 was accompanied by a decrease in the boron carbide content of the stoichiometry formula B13C2 and an increase in the content of TiB2, while the SiC content was almost constant. The relative density of the obtained boron carbide composites, as well as their hardness and resistance to wear, increased with the sintering temperature and TiB2 content. Unfortunately, the reactions occurring during sintering did not allow us to obtain composites with high density and hardness. The relative density was 76-85.2% of the theoretical one, while the Vickers hardness was in the range of 4-12 GPa. The mechanism wear of boron carbide composites tested in friction contact with WC was abrasive. The volumetric wear rate (Wv) of composites decreased with increasing sintering temperature and TiB2 content. The average value of coefficient of friction (CoF) was in the range of 0.54-0.61, i.e., it did not differ significantly from the value for B4C sinters.

Effect of nitrogen addition on sintering behavior of high-entropy alloy CrMnFeCoNi powder

The effect of nitrogen addition on sintering behavior of high-entropy alloy CrMnFeCoNi powder has been investigated. CrMnFeCoNi alloy powders were nitrided to add nitrogen and then consolidated at three different temperatures. The microstructure of the nitrided CrMnFeCoNi alloy powders and sintered compacts was characterized using electron probe microanalysis (EPMA) system. In the compact sintered at 800 °C, a high-nitrogen-content region formed a continuous network structure around the low-nitrogen-content substrate. The hardness of the sintered compacts with nitrogen was higher than that of the compacts without nitrogen. The high-nitrogen-content region expanded into the substrate region. The Vickers hardness of the sintered compacts increased with an increase of sintering temperature up to 950 °C. Sintering at 1100 °C did not completely finish; the vacuum pressure in the sintering chamber rapidly increased because chromium nitride (CrN) decomposed. The results indicate that high-temperature sintering is ineffective for nitrogen-added CrMnFeCoNi alloy powder.

Microwave absorption, thermal and mechanical properties of amorphous nano carbon doped aluminium nitride composite ceramics

Low-cost amorphous nano-carbon (ANC) was employed as an absorbent to modify the microwave performance of AlN ceramics (AlN-4 wt% Y2O3-x wt% C, x = 0, 2.0, 3.8, 3.9, 4.0) via hot-pressing sintering, and the thermal and mechanical properties were also investigated. With the increase of ANC content from 0 to 4.0 wt%, the relative density of AlN composite decreases from 3.28 g cm−3 to 3.16 g cm−3 when sintered at 1800 °C for 2 h, and with the increase of sintering temperature from 1700 °C, the density of the 4.0 wt% ANC doped AlN composite presents trend of increase and reaches the maximum value of 3.16 g cm−3 at 1800 °C and then decreases. The XRD pattern shows that the composites are composed of AlN and Y–Al–O (YAG, YAP, YAM et al.) phases. SEM results indicate that average grain sizes for AlN and secondary phases gradually decrease with increasing carbon content, suggesting inhibited grain growth due to ANC addition. No obvious changes in phase constitution nor intensity changes were detected with the increase in carbon content and sintering temperature. As the carbon content increases from 0 to 4.0 wt%, the dielectric constant gradually increases from ∼9 to 13.89 at 10 GHz, the dielectric loss gradually increases from the vicinity of 10−3 to 0.38 at 10 GHz, and the reflective loss decreases from −27.92 dB to −49.40 dB, the thermal conductivity of the AlN-ANC composite decreases from 116.63 W m−1 K−1 to 50.13 W m−1 K−1. In addition, with 4.0 wt% ANC addition, the dielectric constant, dielectric loss, reflective loss, hardness, elastic modulus, bending strength, and fracture toughness are 13.89, 0.38, 49.40 dB, 6.4 ± 0.4 GPa, 262 GPa, 268.78 MPa, and 1.4 ± 0.1 MPa m1/2, respectively. Its ability to efficiently absorb microwave energy enhances the performance of devices including radar systems, communication equipment, and microwave heating systems, making it a promising candidate for microwave vacuum electronic applications.

Effect of sintering temperature on microstructure and electrical properties of Na0.5Bi0.47Sr0.02TiO3-δ ceramics

In this investigation, a series of Na0.5Bi0.47Sr0.02TiO3-δ samples, sintered from 1000 to 1100 °C, were synthesized utilizing the solid-state method. The XRD results indicate that all samples exhibit a perovskite phase, with the exception of those sintered at 1100 °C, which display no discernible impurity peaks. The SEM results indicate that the average grain size exhibits an increase proportionate to the sintering temperature, which attributes to the variations in the actual Na/Bi ratio. From the study of grain conductivity we can obtain that the dominant factor affecting grain conductivity is the activation energy. At 1100 °C, the oxygen vacancy concentration emerges as the primary determinant of grain conductivity. It should be noticed that the phase transition temperature of the sample increases (350 °C→400 °C) with the increase of sintering temperature, which is due to the local A-site disorder aggravated by high temperature sintering. Therefore, reducing the sintering temperature is beneficial to improve the grain conductivity. The grain boundary conductivity initially rises, then diminishes with increasing sintering temperature. It is evident that the enhanced macroscopic grain boundary conductivity stems from a marked reduction in space charge potential within the 1000–1025 °C temperature range. Within the 1050 °C−1100 °C temperature range, the space charge potential barely changed, the significant decrease of intrinsic grain boundary conductivity can be attributed to the surge in the coverage ratio of grain boundary impurities and the number of grain boundary impurities increased caused by the rapid reduction of grain boundary area and thermal evaporation. The research on electrical performance of NBT-based oxygen-ion conductors will promote the application of NBT-based oxygen ion conductors in solid oxide fuel cells, oxygen sensors and other fields.

The effect of degree of sintering on the structural and mechanical properties of Si3N4–SiO2 glass ceramics

Silica-based glass ceramics have been extensively used in biomedical applications due to their superior biocompatibility and controllable properties. However, their low mechanical strength limits their application. This could be addressed by optimizing the crystalline phase which determines their final properties. Silicon nitride has attracted attention due to its combination of good mechanical and biological properties. Therefore, to combine the advantage of silica-based glass and silicon nitride ceramic, this study developed a silicon nitride-silicon dioxide (Si3N4–SiO2) glass ceramics. The effects of spark plasma sintering parameters on the structural and mechanical properties of Si3N4–SiO2 glass ceramics were investigated. Full densification was reached at a sintering temperature of 1300 °C, a holding time of 10 min and an applied pressure of 80 MPa (relative density = 99.19 %). No silicon oxynitride (Si2N2O) crystalline phase was formed in the sintered glass ceramics, as confirmed by XRD. The interface between the β-Si3N4 crystalline and amorphous SiO2 was investigated by HRTEM, and the results indicated that an amorphous interfacial oxide was formed at the interface. The mechanical properties increased with increasing sintering temperature, as a result of the increased density. The Si3N4–SiO2 glass ceramics sintered at 1500 °C exhibited the highest value of toughness and flexural strength, at 4.6 ± 0.28 MPa m1/2 and 360 ± 27 MPa. The indentation cracks observed by SEM showed that the large β-Si3N4 grains promoted crack deflection, while the equiaxed Si3N4 grains with a lower aspect ratio led to transgranular fracture. The mechanical properties of these Si3N4–SiO2 glass ceramics are comparable to commercial glass ceramics, indicating their promising aspects in biomedical applications.

Effect of Various Sintering Temperatures on the Friction and Mechanical Properties of PEEK/PTFE Blends

Polytetrafluoroethylene (PTFE) has a very low coefficient of friction and outstanding corrosion resistance, but its limited use is due to high wear and tear and low hardness. Polyetheretherketone (PEEK) offers low wear, high temperature resistance and a slightly higher coefficient of friction. In the research we describe here we examined the mechanical and tribological properties of PEEK/PTFE blends manufactured at various sintering temperatures (350 °C–390 °C). The experimental data demonstrated that the PEEK/PTFE blends exhibited the highest tensile strength, 22.97 Mpa, when sintered at 380 °C, making them the most resistant to breaking or deforming. The elongation at break increased with the increase of sintering temperature, and the highest value of elongation at break for the PEEK/PTFE blends was 429.16% when sintered at 390 °C, and the lowest value was 283.37% when sintered at 350 °C. The PEEK/PTFE blends exhibited the lowest coefficient of friction, measuring 0.174, when sintered at 350 °C. The lowest mass abrasion rate for the PEEK/PTFE blends was 6.04 × 10−7 mm3/N·m when sintered at 360 °C.

Influence of sintering temperature on electrocaloric and energy storage properties of sol-gel derived lead-free BaHf0.20Ti0.80O3 ferroelectric ceramics for sustainable energy solutions

Ferroelectric materials have emerged as intriguing contenders for a variety of applications in the ongoing effort to look for sustainable energy solutions, including energy storage and solid-state cooling systems. In this work, a systematic investigation has been conducted on the microstructural, dielectric, electrocaloric, and energy storage characteristics of sol-gel elaborated BaHf0.20Ti0.80O3 (BHT) ferroelectric ceramics. The structural investigation by Raman and X-ray diffraction indicated that when the sintering temperature increases, the tetragonality of BHT ceramics reduces, and the evolution of the cubic phase increases. The evolution of the microstructure in BHT ceramics is found to be significantly reliant on the sintering temperature. With increasing temperature of sintering, the bulk density of BHT ceramics increases. The improved dielectric and ferroelectric properties were attained in BHT ceramics at higher sintering temperatures. The BHT ceramic sintered at 1350 °C exhibited a maximum electrocaloric temperature change of ΔT ∼0.6 °C with a corresponding efficiency ΔT/ΔE of 0.3 K mm/kV near ambient temperature under a low electric field of 20 kV/cm. The BHT ceramic sintered at 1450 °C exhibited excellent room temperature recoverable energy density of JRec ∼67.84 10−3J/cm3 and high energy storage efficiency of η ∼75.13 % under a low electric field of 20 kV/cm. The highest JRec ∼73.22 10−3J/cm3 with corresponding η of 64.60 % were obtained in BHT ceramic sintered at temperature 1350 °C. These findings broaden the possibility of exploring BHT-based systems as efficient lead-free ferroelectrics for both solid-state refrigeration and energy storage applications.

Effect of phase evolution and pyroplastic formation behavior on glass-ceramic foam derived from silicomanganese slag and feldspar tailings

Utilizing solid waste to produce foam material has become a significant direction in resource recycling. This study focuses solely on using silicomanganese slag and feldspar tailings as raw materials, utilizing a powder sintering process to produce autocatalytic foaming glass–ceramic foam. We formulated four mix ratios based on the compositional characteristics of the silicomanganese slag and feldspar tailings. The study then explored the evolution of phase formation and macroscopic pore morphology under varying preparation temperatures. Moreover, through multi-phase co-melting experiments, this work unveiled the high-temperature molten mass generation mechanism between silicomanganese slag and feldspar tailings. Our findings reveal that the glass melt generated from silicomanganese slag particles and the 'solid–liquid erosion behavior' of feldspar particles play pivotal roles in the formation of high-temperature co-melt substances. As the sintering temperature increases, the mixed powder exhibits three different states of high-temperature molten mass, which are the reasons for the evolution of the macroscopic pore structure. It is suggested that the addition of silicomanganese slag should be less than 50 %, and the heat treatment temperature should be below 1145 °C in preparing glass–ceramic foam with silicomanganese slag and feldspar tailings. The sample with 40 % silicomanganese slag and 60 % feldspar tailings, treated at 1140 °C, yielded glass–ceramic foam with a compressive strength of 1.68 MPa, apparent density of 0.279 g/cm3, porosity of 81.7 %, and thermal conductivity of 0.074 W·m−1·K−1. In summary, this study provides a novel approach for the high-value utilization of silicomanganese slag and offers an economical route for developing lightweight, eco-friendly structural materials.

Isostatic hot-pressed tungsten radiation shields against gamma radiation

An isostatic hot-pressing technique for the fabrication of dense W samples' is presented. The samples’ microstructure and chemical content were analyzed. The most compact samples were received at 5 GPa pressure and 1500 and 2000 °C temperatures, with densities of 18.50 and 19.07 g/cm3, respectively. It has been established that high temperature exposure has a positive effect on both the microstructure and density. It is shown that as the sintering temperature increases, the porosity of the samples decreases from 32.31% to 0.94%, and their relative density increases from 67.69% to 99.06%. The crystal structure investigation revealed that all the samples contain the main body-centered cubic W phase, and the availability of the WO2 phase is observed just after the temperature of sintering increases above 1000 °C, which is confirmed by the appearance of 111 and 22-2 reflections. A study of the shielding effectiveness against gamma-radiation was carried out using the Phy-X/PSD software. A gamma-ray source of Co60 with energies of 0.8–2.5 MeV was applied for the calculations. The results were calculated for the sample with the highest density (19.07 g/cm3) and compared with the calculations for Pb. The W shielding effectiveness main parameters are determined: linear attenuation coefficient (at 0.8 MeV–1.46 cm-1), mean free path (at 2.5 MeV–1.2 cm) and half value layer (at 2.5 MeV–0.86 cm). These values turned out to be higher than for Pb, which makes shields based on W promising for use in the field of radiation protection.

Elastoplastic nanoindentation behaviors of sintered nano-silver under various sintering parameters

Purpose This study aims to characterize the mechanical properties of sintered nano-silver under various sintering processes by nano-indentation tests. Design/methodology/approach Through microstructure observations and characterization, the influences of sintering process on the microstructure evolutions of sintered nano-silver were presented. And, the indentation load, indentation displacement curves of sintered silver under various sintering processes were measured by using nano-indentation test. Based on the nano-indentation test, a reverse analysis of the finite element calculation was used to determine the yielding stress and hardening exponent. Findings The porosity decreases with the increase of the sintering temperature, while the average particle size of sintered nano-silver increases with the increase of sintering temperature and sintering time. In addition, the porosity reduced from 34.88%, 30.52%, to 25.04% if the ramp rate was decreased from 25°C/min, 15°C/min, to 5°C/min, respectively. The particle size appears more frequently within 1 µm and 2 µm under the lower ramp rate. With reverse analysis, the strain hardening exponent gradually heightened with the increase of temperature, while the yielding stress value decreased significantly with the increase of temperature. When the sintering time increased, the strain hardening exponent increased slightly. Practical implications The mechanical properties of sintered nano-silver under different sintering processes are clearly understood. Originality/value This paper could provide a novel perspective on understanding the sintering process effects on the mechanical properties of sintered nano-silver.

Tailoring tactics for preparation of superior thermal insulation materials from blast furnace ferronickel slag: Control of sintering temperature

Blast furnace ferronickel slag (BFFS) was converted to thermal insulation materials by sintering of its mixture with 15 wt% fly ash cenosphere (FAC) from 1000 °C to 1200 °C. The influence of sintering temperature on the phase compositions, microstructures, and properties of the materials was investigated based on both thermodynamic and experimental analyses. It was demonstrated that increasing sintering temperature from 1000 °C to 1200 °C led to linear increases of contents of diopside (CaMgSi2O6; y = 0.039T – 21.5, where y and T denote the content and temperature, respectively), anorthite (CaAl2Si2O8; y = 0.0504T – 46.54), and magnesium aluminate spinel (MgAl2O4; y = 0.043T – 30.86) in the thermal insulation materials. Meanwhile, there existed linear decreases of contents of akermanite (Ca2MgSi2O7; y = -0.0352T + 66.18) and gehlenite (Ca2Al2SiO7; y = -0.0914T + 129.96), which could form a solid solution above 1100 °C, suppressing the expansion associated with the generation of magnesium aluminate spinel. Along with the phase transformation, the macroporous structure was also identified. By sintering at 1100 °C for 2 h, an optimal high-quality thermal insulation material with apparent porosity of 46.04%, water absorption of 42.12%, bulk density of 1.35 g/cm3, linear shrinkage of 0.82%, compressive strength of 6.83 MPa, thermal conductivity of 0.31 W/(m·K) at 25 °C and 0.42 W/(m·K) at 800 °C, and refractoriness of 1259 °C could be obtained.

Preparation and properties of in situ TiC/corundum–mullite electrically conductive ceramic

AbstractIn situ TiC/corundum–mullite electrically conductive ceramics were prepared by carbon‐bed sintering method using bauxite, clay and Ti3SiC2 powders as raw materials. The phase composition, microstructure, shrinkage, apparent porosity, bulk density, compressive strength, and resistivity of samples were investigated. The X‐ray diffraction results indicate that the TiC is completely generated by desilicidation reaction of the Ti3SiC2 at 1 300°C. When the sintering temperature is 1 300°C and Ti3SiC2 powder addition is 22 wt.%, the properties of the sample are optimum, with a longitudinal shrinkage of 2.04%, a radial shrinkage of 2.56%, an apparent porosity of 19.01%, a bulk density of 2.53 g/cm3, a compressive strength of 181 MPa, and a resistivity of 267 Ω·cm. The electrically conductive phase TiC is connected into a complete electrically conductive network. The shrinkages of samples decrease with increasing sintering temperature, which indicates that the samples expand due to secondary mullitization. The continuous electrically conductive network of TiC is destroyed. As the Ti3SiC2 powder addition increases from 14 to 20 wt.%, the resistivity of the samples decreases significantly, but the further increase in the Ti3SiC2 powder addition has no significant effect on the resistivity.

Examining the effects of sintering temperature on double perovskite La2NiTiO6: Analysis of structural, optical, electrical properties, and leakage current characteristics

This study explores the influence of varying sintering temperatures on the structural, optical, electrical, and leakage current features of La2NiTiO6 (LNTO), a double perovskite material synthesized through the citrate auto-ignition method. The X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), and energy dispersive X-ray (EDX) analysis were employed to investigate the structure, microstructure, and compositional distribution of the samples. The samples sintered at various temperatures showed the monoclinic structure with space group P21/n and were confirmed by Rietveld's refinement of the XRD patterns. The average grain size increased with higher sintering temperatures, which is consistent with the particle size estimated from the histogram plot of the FE-SEM data. The UV–visible (UV–Vis) spectroscopy showed that the energy band gap decreased as sintering temperatures increased. Impedance spectroscopy analysis revealed non-Debye type relaxation of charge carriers and confirmed the negative temperature coefficient of resistance (NTCR) behavior. Electrical analysis affirmed that the direct current (DC) conductivity is thermally activated, following the Arrhenius equation with an inverse temperature dependency. As the sintering temperature increases, the leakage current density decreases, and the leakage current conforms to the ohmic conduction mechanism.

Investigation of physical and metallographic properties of nickel matrix composite by ultrasonic method

Ultrasonic testing (UT) is one of the most widely used non-destructive testing techniques for the characterization and evaluation of materials. In this study, the material properties of AstCrM-BN-Cr-Ti-Ni composites produced by mechanical mixing and electroless nickel plating technique were evaluated using UT. Changes in ultrasonic wave velocity, Young's modulus, density, porosity and hardness are observed in the heat-treated material at different temperatures. Samples analyzed by Scanning Electron Microscopy (SEM) and X-Ray Diffractometry (XRD) exhibited changes in grain structure at different sintering temperatures. It has been observed that the change in grain size also affects mechanical and physical properties according to ultrasonic properties. In conclusion, the experimental results showed a linear relationship between the mean grain size and the UT parameters (ultrasonic longitudinal and transverse velocity, Young's modulus), physical (sintering temperature and density) and mechanical properties (hardness and porosity) of the material. Grain growth occurs with increasing sintering temperature, porosity content decreases, hardness, Young's modulus and ultrasonic wave velocity values also increase.