Precursor Powders Research Articles

Calcination-based direct extraction of hydroxyapatite from bovine bone waste

ABSTRACT The main chemical components of waste cow bones are apatite minerals, especially those containing calcium and phosphorus. This study investigated whether this bone could produce extracted hydroxyapatite through calcining at 900° C for different holding times (1–6 h). An average mass loss of 45% occurred in this experiment during the preparation of bone powders, which involved crushing and further calcining at this temperature. The quantitative XRD analysis showed that 99.97 wt.% hydroxyapatite and over 0.3 wt.% calcite were present in the raw and as-calcined bone powders, with trace amounts of CaFe3O5 (calcium ferrite) phases appearing in the calcined product. Depending on the holding calcining times, SEM images of the calcined bovine powders revealed aggregate sizes ranging from 0.5–3 µm and crystallite (grain) sizes ranging from 70 to 340 nm in all calcium-phosphate powder products. Following EDX analysis of all sample surfaces, possible calcium-deficient hydroxyapatite instead of hydroxyapatite formed, as evidenced by the calcined product's Ca/P ratio exceeding 1.67. Additionally, calcining cow bones for 5–6 h at 900° C yielded a high-purity nano-crystalline hydroxyapatite powder precursor in biomedical applications.

Influences of oxygen partial pressure on the phase composition of the (Bi, Pb)-2212 precursor powder

Bi-2223 tapes, synthesized through the two-powder method, exhibit distinctive features such as high current density and a controllable secondary phase. Traditionally, the two-powder method involves the separate preparation of Bi-2212 and CaCuO powders followed by their mixing. However, during this process, it is necessary to dope the Bi-2212 powder with an appropriate Pb content to achieve a stable lattice structure in the Bi-2223 phase. The alteration of ion valences between Pb2+ and Pb4+ influences the oxygen content, thereby affecting the phase formation of (Bi, Pb)-2212 and, consequently, the final properties of Bi-2223 tapes. Surprisingly, limited research has explored the impact of the heat treatment process on (Bi, Pb)-2212. Consequently, this study investigates the phase composition and microstructure of (Bi, Pb)-2212 under various oxygen partial pressures to deepen our understanding of the effect of Pb on the composition of (Bi, Pb)-2212. Simultaneously, the behavior of Pb in the lattice of Bi-2212 is analyzed. Ultimately, the findings reveal that low oxygen conditions are advantageous for fabricating (Bi, Pb)-2212 powder with a high main phase content and a reduced secondary phase, thereby demonstrating excellent current-carrying performance in Bi-2223 tapes.

One-step synthesis and low-temperature rapid sintering of alumina-zirconia ceramics by flash sintering combined with phase transformation

High-performance alumina-zirconia ceramics are generally sintered above 1500 °C and consume lots of energy; rapid sintering at low temperature is an ideal technique due to its economy and low-energy consumption. For the first time, flash sintering combined with phase transformation-assisted sintering techniques was reported in this work. The alumina-zirconia amorphous precursor powder was used to replace the final product powder for ceramic processing, and the one-step synthesis and rapid sintering densification of alumina-zirconia ceramics at low temperature of 849 °C for 60 s were realized. The effects of electric field on the low-temperature sintering of amorphous powders are summarized into three aspects. Firstly, the electric field reduces the viscosity of the amorphous powder and promotes liquid phase sintering. Secondly, the electric field promotes the phase transition of the amorphous powder from metastable to stable phase, and accelerates the atomic migration. Thirdly, Joule heating and defect generation in the flash sintering promotes more effective material transport. Overall, this work reduces the energy for calcination of amorphous powders, reduces the sintering temperature of ceramics, well hinders the grain coarsening and shows excellent mechanical properties.

Recent Advances in Spin-coating Precursor Mediated Chemical Vapor Deposition of Two-Dimensional Transition Metal Dichalcogenides.

Two-dimensional (2D) transition metal dichalcogenides (TMDs) have garnered widespread interest in the scientific community and industry for their exceptional physical and chemistry properties, and great potential for applications in diverse fields including (opto)electronics, electrocatalysis, and energy storage. Chemical vapor deposition (CVD) is one of the most compelling growth methods for the scalable growth of high-quality 2D TMDs. However, the conventional CVD process for synthesis of 2D TMDs still encounters significant challenges, primarily attributed to the high melting point of precursor powders, and achieving a uniform distribution of precursor atmosphere on the substrate to obtain controllable smaple domains is difficult. The spin-coating precursor mediated chemical vapor deposition (SCVD) strategy provides refinement over traditional methods by eliminating the use of solid precursors and ensuring a more clean and uniform distribution of the growth material on the substrate. Additionally, the SCVD process allows fine-tuning of material thickness and purity by manipulating solution composition, concentration, and the spin coating process. This Review presents a comprehensive summary of recent advances in controllable growth of 2D TMDs with a SCVD strategy. First, a series of various liquid precursors, additives, source supply methods, and substrate engineering strategies for preparing atomically thin TMDs by SCVD are introduced. Then, 2D TMDs heterostructures and novel doped TMDs fabricated through the SCVD method are discussed. Finally, the current challenges and perspectives to synthesize 2D TMDs using SCVD are discussed.

Inorganic Fullerene-Like WS2 Reinforced Polyamide Powders for Improved Mechanical Properties in Laser Sintered Nanocomposite Parts

Polyamide (PA) is a widely utilized engineering polymer, and its thermal and mechanical properties can be further improved by adding nanofillers. However, adding inorganic fullerene-like tungsten disulfide (IF-WS2) nanoparticles (NPs) to PA to produce composite precursor powders for additive manufacturing is challenging. Here, we report a novel and cost-effective method for fabricating PA-12 based nanocomposite (NC) powders with fixed/partially encapsulated IF-WS2 nanoparticulate fillers utilizing an advanced mixing technique because simple wet mixing (WM) can only attach fillers weakly to the powder surfaces when compared to the proposed method. The resulting nanocomposite powders maintained nearly the original particle size distribution of PA-12. They also exhibited improved rheological properties, melting, and crystallization behaviors compared with those prepared by the WM method. The laser-sintered PA-12 nanocomposite specimens revealed enhanced powder thermal stability and higher tensile strengths than pristine PA-12, validating the advantages of the novel technique for the fabrication of polyamide nanocomposite powders and their suitability for utilization in laser sintering additive manufacturing. These results demonstrate that high-performance engineered PA-12 nanocomposite components can be directly laser sintered, and this technique can potentially be extended to fabricate other engineered polymeric nanocomposite powders.

Introducing an Efficient and Eco-Friendly Spray-Drying Process for the Synthesis of NCM Precursor for Lithium-ion Batteries

<p>Ni-rich cathode is one of the promising candidates for high-energy lithium-ion battery applications. Due to its specific capacity, easy industrialization, and good circulation ability, Ni-rich cathode materials have been widely used for lithium-ion batteries. However, due to the limitation of the co-precipitation method, including sewage pollution, and the instability of the long production cycles, developing a new efficient and environmentally friendly synthetic approach is critical. In this study, the Ni<sub>0.91</sub>Co<sub>0.06</sub>Mn<sub>0.03</sub>CO<sub>3</sub> precursor powder was successfully synthesized by an efficient spray-drying method using carbonate compounds as a raw material. This Ni<sub>0.91</sub>Co<sub>0.06</sub>Mn<sub>0.03</sub>CO<sub>3</sub> precursor was calcined by mixing with LiOH·H<sub>2</sub>O (5 wt% excess) at 480°C for 5 hours and then sintered at two different temperatures (780°C/800°C) for 15 hours under an oxygen atmosphere to complete the cathode active material preparation, which is a key component of lithium-ion batteries. As a result, LiNi<sub>0.91</sub>Co<sub>0.06</sub>Mn<sub>0.03</sub>O<sub>2</sub> cathode active material powders were obtained successfully via a simple sintering process on the Ni<sub>0.91</sub>Co<sub>0.06</sub>Mn<sub>0.03</sub>CO<sub>3</sub> precursor powder. Furthermore, the obtained LiNi<sub>0.91</sub>Co<sub>0.06</sub>Mn<sub>0.03</sub>O<sub>2</sub> cathode active material powders were characterized. Overall, the material sintered at 780°C shows superior electrochemical performance by delivering a discharge capacity of 190.76mAh/g at 1<sup>st</sup> cycle (0.1 C) and excellent capacity retention of 66.80% even after 50 cycles.</p>

System and Method for One or More Extruders Using a Robotic Arms to Print a 3D Model

The need for creating realistic body parts and anatomical models using additive printing was long ago recognised. The paper "Rapid prototyping approaches for anatomical modelling in medicine" by M. McGurk et al. in Ann. R. Coll. Surg. Engl. 1997; 79; 169-174, which discussed 3-D printing of models, summarised the state of the art in this subject some years ago. Models were made by sprinkling liquid over a layer of precursor powder using inkjet printer nozzles to form a solid, thin slice. For each additional slice, the printing procedure was repeated until the item was finished as a "green state" component, which was then burned in a furnace to sinter it. The product was then subjected to further processing to create a full density portion. Large item 3D printing has been simpler than in previous years because to the development of software for computer controlled robotic XY motion systems used in the semiconductor and optical sectors. Layered building of 3D things is now a comparatively cheap and quick operation for 3D printing equipment thanks to software applications like SolidWorks, AutoCAD 360, and similar software products. Larger things may be 3D printed by either attaching rails above the print nozzles for X-Y motion directed from above the nozzles, or by positioning the object to be created on an X-Y table with motion supplied below the nozzles. The current work attempts to construct a 3D printing setup that utilises two robotic arms to print a single component. Here, the bed will be swivelled to a specific angle to prevent the robotic arms from becoming entangled, and the robotic arms will also move 180 degrees from their mean positions. Additionally, the related software will be developed locally in our lab, resulting in a shorter printing time and higher level of accuracy.

High-performance thermoelectric properties of Cu2Se fabricated via cold sintering process

The concept of a ‘phonon-liquid electron-crystal’ has received significant interest in recent years, with copper selenide (Cu2Se) emerging as one of the high-performance thermoelectric materials within this framework. This study focuses on the fabrication of Cu2Se bulk pellets through a low-temperature sintering method known as cold sintering process (CSP). The introduction of a liquid phase (thiol-amine solution) in this process facilitates the dissolution and precipitation of ion/atom clusters, resulting in sample densification. Remarkably, a sample density of nearly 90 % is achieved at a low sintering temperature of only 473 K. Furthermore, this CSP approach preserves the morphology of the Cu2Se precursor powders and effectively inhibits grain growth. Consequently, the lattice thermal conductivity of the CSP samples is significantly reduced, attributed to enhanced grain boundary phonon scattering. This leads to a substantial improvement in the figure-of-merit (ZT), increasing from 0.65 at 800 K in the hot-pressed sample to 2.13 at 800 K in the CSP sample. The advantages of CSP can be extended beyond Cu2Se, as it holds promise for enhancing the performance of various high-performance thermoelectric materials.

Investigation of the effect of impurity of precursor materials on Si‐doped boron carbide properties

AbstractBoron carbide is a notable ceramic, with its high hardness and low density. However, it suffers a sudden loss in strength under high shear stress. Doping boron carbide with Si/B is widely used to increase its resistance to amorphization. High purity boron and silicon hexaboride precursor powders are used for doping boron carbide, but these materials have high costs and supply chain constraints. This research investigated the effect of substituting lower purity B or using pure Si powder instead of SiB6 on materials’ properties such as elastic and mechanical properties, microstructure, and amorphization resistances. It was observed that using lower‐purity boron or pure Si powder instead of SiB6 did not significantly affect critical properties, such as fracture toughness, hardness, or amorphization resistance. However, Young's modulus values decreased as B purity decreased and as Si was used instead of SiB6. These findings demonstrate that substituting precursor materials in Si/B co‐doped B4C is possible with little change in the material's properties. This facilitates the use of easier‐to‐access, cheaper production routes to be used for silicon‐doped boron carbide products.

Solventless mechanochemical synthesis of Sn-based halide perovskite microcrystals with high stability tracked by photoluminescence spectroscopy

Developing solvent-free methods to synthesize lead-free perovskites is of practical importance from the viewpoint of sustainability. In this work, we use a facile mechanochemical approach to synthesize a series of lead-free Sn-based halide perovskite microcrystals (powders) in ambient conditions directly from precursor powders (CsX and SnX2 (X = I, Br, Cl)) without any solvent. Such an approach is energy-saving and avoids the use of toxic solvents. There exists phase evolution during the mechanochemical processing of the precursor powders with CsSn2Br5 to CsSnBr3 in the first hour and finally into the stabilized phase of Cs2SnBr6 after 28 days and with Cs2SnCl4 to CsSnCl3 in the first hour and finally to the stabilized phase of Cs2SnCl6 after 36 days. The stabilized Cs2SnI6 powders emit light centered at 930 nm under the excitation of 785 nm, and the stabilized Cs2SnBr6 powders emit light centered at 682 nm under the excitation of 365 nm. Both the stabilized Cs2SnI6 and Cs2SnBr6 powders exhibit excellent long-term structural and optical stabilities, and the Cs2SnBr6 powders have a better thermal stability than the Cs2SnI6 powders. This work likely offers a green-route synthesis of lead-free halide perovskites towards large-scale manufacturing and industrialization.

Process optimisation of alumina coatings by modification of powder characteristics in the aerosol deposition method

The aerosol deposition process, involving the impact of solid particles on a substrate at high velocities, is an attractive method for the manufacture of ceramic coatings at room temperature. For process optimisation, it is crucial to select a powder having the appropriate physical characteristics and evaluate the particle flow behaviour during the deposition process. In this study, a powder modification process using high-energy milling and spray drying to improve the applicability of precursor powders was developed and evaluated both numerically and experimentally. A modified aerosol deposition system incorporating a brush-type aerosol generator was employed to maintain the continuity of the aerosol supply and improve the stability of the particle concentration. The deposition efficiency was nearly tripled when using spray-dried granules (0.68%) instead of the as-received powders (0.26%). From tribological measurements, the strongest interfacial bonding was also confirmed for coatings prepared with alumina granules.

(Digital Presentation) Facile Fabrication of Nickel and Sc-Doped Zirconia Cermet Electrode Thin Film on YSZ Substrate Via Screen-Printing for Solid Oxide Electrochemical Cells

Solid oxide electrochemical cells (SOCs) operating as either solid oxide fuel cells (SOFCs) or solid oxide electrolysis cells (SOECs) are widely known as promising advancements in green energy technologies for storage and high-efficiency energy generation. This study used a single screen-printing deposition method to fabricate a porous Nickel – scandia-stabilized zirconia (Ni-ScSZ) cermet electrode on a dense YSZ solid electrolyte substrate. The precursor powders were prepared via the glycine-nitrate combustion process. To investigate the effect of ink slurry solvent on the quality, structure, and morphology of the deposited films, ethanol, and alpha-terpineol were used. The screen-printed films were sintered at 1300°C for 6h and reduced under an Ar/5% H2 gas environment at 700°C for 2h to form porous electrodes. X-ray diffraction (XRD) analysis showed that all sintered NiO-ScSZ films exhibited cubic peak structures of both NiO and ScSZ. Scanning electron microscopy (SEM) micrographs and elemental mapping revealed finer morphology with good dispersion of NiO and ScSZ phases for sintered NiO-ScSZ films with alpha-terpineol as solvent. After exposure to Ar/5% H2 gas environment, a complete reduction of NiO to Ni was revealed by XRD for all Ni-ScSZ electrodes. Moreover, SEM micrographs of as-reduced samples showed an increase in porosity as oxygen was removed from NiO. Electrochemical impedance spectroscopy was used to determine the conductivity of the reduced Ni-ScSZ electrode films under Ar/5% H2 gas environment. The obtained total conductivity values upon reduction are 9.54x10-5 S/cm and 4.75x10-5 S/cm for ethanol and alpha-terpineol as solvents, respectively.

Interfacial Chemical Stability of Doped Li7-XLa3Zr2 -X(Nb/TaX)O12 with LiCoO2 Electrode Material

Garnet-type oxide solid state electrolytes (SEs) are promising candidates due to their potential high ionic conductivity and chemical stability with Li for the replacement of flammable liquid electrolytes used in the current Li-ion batteries. Intense research has been focused on optimising the interface of garnets with Li, with the positive side to be somehow neglected. A significant issue of oxide SEs, hurdling their industrial application, is their poor contact with positive materials due to their rigidity. Poor interfacial contact leads to the need of co-sintering at high temperatures (> 400 °C), which enables side reactions and unwanted processes like cation intermixing, diffusion of elements and formation of non-conductive secondary mixed phases.In this work the chemical stability of Ta and Nb doped LLZO garnet SE was tested in contact with LiCoO2, a common positive material used in the battery industry. Initially, mixed powders of SE and active material were heat treated and studied using Raman spectroscopy and scanning electron microscopy to observe side reactions. In order to improve contact between the two materials, instead of already synthesized crystalline powder, nitrate precursors were also used for in-situ synthesis of LiCoO2 material in contact with the garnet. Mixtures of the SE powder and nitrate precursors for LiCoO2 were also heat-treated at various temperatures for different time periods in different gas atmospheres. The heat-treated materials were then analysed extensively using scanning electron microscopy coupled with energy dispersive X-Ray element mapping and with Raman microscopy to prove the existence or absence of secondary mixed phases at given conditions. Additionally, the optimized heat-treatment conditions were adapted for layered garnet SE/LiCoO2 samples to study the actual electrolyte/electrode interface at the same conditions used for powder mixtures. Based on the results the symmetrical LiCoO2/garnet SE/LiCoO2 cells will be prepared and tested electrochemically.

(Digital Only Presentation) Effects of Ink Solvent on the Screen-Printing Fabrication and Morphology of LSM-YSZ Thin Films Deposited on YSZ Substrate for Solid Oxide Electrochemical Cells

Screen-printing is a cheap and easy thin film deposition technique utilized in energy devices fabrication, specifically, in solid oxide electrochemical cells (SOCs). This technique offers simple set-up, film quality control and mass production. In this study, LSM-YSZ, a promising component material for SOCs application was deposited on YSZ electrolyte via screen-printing. Specifically, the study aimed to investigate the effect of the solvent used in screen-printing on the quality of the deposited film. LSM-YSZ precursor powders synthesized via glycine-nitrate combustion process (GNP) were screen-printed on YSZ substrate using different solvents, ethanol and alpha-terpineol. The structure, morphology, and conductivity values of the GNP LSM-YSZ thin films using two solvents were compared. Results showed that both solvents produced a uniform distribution of rhombohedral LSM and cubic YSZ thin films with porous morphologies but alpha-terpineol solvent exhibited more agglomerated particles. Despite having this morphology, alpha-terpineol is still preferred than ethanol due to its reproducibility and scalability as it is less volatile than the other one. Moreover, there was no significant difference between the measured total conductivities of the half-cells using two solvents with the values of 4.63e-3 S/cm and 2.07e-3 S/cm at 700°C, and activation energies of 0.374 eV and 0.483 eV from 500°C - 700°C, for ethanol and alpha-terpineol, respectively.

BN6BT ceramics via cold‐sintering with annealing: Effects of grain size of precursor powders and annealing temperature

AbstractIn this work, (Bi0.5Na0.5)0.94Ba0.06TiO3 (BN6BT) lead‐free ceramics were prepared via cold‐sintering followed by annealing, and effects of grain size of precursor powders and annealing temperature on microstructure, dielectric, and ferroelectric properties of the ceramics were studied. The precursor powders for cold sintering were obtained by mixing the powders with sub‐micrometer (average grain size, AGS = 0.26 μm) and nanometer (AGS = 73 nm) grains in various mass ratios (1:0, 1:1, 1:2, and 1:4). The precursor powders were mixed with deionized water and cold sintered at 180°C for 1 h under 500 MPa. The cold‐sintered samples were then annealed at temperatures between 800 and 1000°C for 2 h. For the ratios of 1:2 and 1:4, the corresponding ceramics annealed at 950°C exhibit dielectric and ferroelectric properties similar to those of the BN6BT ceramics sintered at 1170°C via the solid‐state sintering method. The present BN6BT ceramics exhibit dense microstructure with finer grains with AGS = 280 nm, higher breakdown strength (BDS = 160 kV· cm−1) compared to the solid‐state sintered BN6BT ceramics with AGS = 1.6 μm and BDS = 75 kV· cm−1. The results demonstrate that the cold‐sintering followed by annealing is effective in preparing BN6BT ceramics with fine grains and excellent dielectric and ferroelectric properties at relatively low temperatures.

Novel refractory high-entropy metal-ceramic composites with superior mechanical properties

A new concept of refractory high-entropy metal-ceramic composites (HEMCC) has been proposed that combines the outstanding physical properties of both high-entropy alloy (HEA) and high-entropy ceramic (HEC). As the first HEMCC system, to the best of our knowledge, TiTaNbZr-(TiTaNbZr)C, has been developed by a powder metallurgy process. The HEA and HEC phases exhibit body-centered cubic (BCC) and rock-salt B1 crystal structures, respectively, and both phases have non-equimolar chemical compositions. With the increase of the HEC phase in HEMCC, the hardness is enhanced while the density and fracture toughness are decreased. HEA50C sintered from 50 vol% HEA and 50 vol% HEC precursor powders shows a favorable combination of flexural strength (541 ± 48 MPa) and fracture toughness (6.93 ± 0.27 MPa·m1/2) at room temperature and a high compressive strength at 1300 °C (275 MPa). The optimized mechanical performance of HEMCC might be attributed to the combination of the ductile HEA and strong HEC phases, smaller grain size, and crack arrest at HEC/HEA interfaces.

A novel dissolution-precipitation strategy to accelerate the sintering of yttrium oxide dispersion strengthened tungsten alloy with well-regulated structure

In this work, accelerated sintering of Y2O3 dispersion strengthened tungsten alloy with a well-regulated structure was achieved by a novel dissolution-precipitation strategy. As indicated, yttrium oxide was firstly dissolved into the lattices of W powder precursor during the thermal plasma synthesis process in a one-step and ultra-fast way, and then homogeneously precipitated out within W grains during sintering. The theoretical calculation reveals that the formation process of Y2O3 dispersoids enhanced the driving force of densification by increasing the sintering stress and declining the macroscopic viscosity, resulting in improved diffusion ability for the W skeleton. The microstructural investigation further confirmed the occurrence of mass inter-diffusion at the W-Y2O3 interface, which provides a fast diffusion pathway for W atoms, and is responsible for the accelerated densification kinetics. Being sintered at 1600 °C for 1 h, the as-obtained alloy possesses a high relative density of 98.26%, together with a refined grain size of 970 nm for W and 50 nm for intragranular Y2O3, respectively.

Structures, dielectric properties and AC impedance characteristics of BiFeO3–BaTiO3 high-temperature lead-free piezoceramics synthesized by the hydrothermal method

Among the lead-free piezoceramics, ([Formula: see text])BiFeO[Formula: see text]BaTiO3 (BF-BT) is considered a promising candidate for high-temperature piezoelectric materials owing to its high Curie temperature ([Formula: see text]C) and good electromechanical properties. In this work, the hydrothermal synthesis method was used to prepare the precursor powders of BiFeO3 and BaTiO3, and then the mixed powder compacts with the chemical composition of 0.7BF–0.3BT were sintered under pressureless conditions. The influence of the hydrothermal reaction times (12–24[Formula: see text]h) of BiFeO3 on the structures and electric properties of the sintered ceramics was instigated. First, all the samples synthesized with the tetragonal BaTiO3 and BiFeO3 powders were identified with relatively stable dielectric properties. As the hydrothermal reaction time to synthesize BiFeO3 increased, the dielectric properties as well as the temperature stability of the 0.7BiFeO3–0.3BaTiO3 ceramics also improved. At the condition of a hydrothermal reaction time of 24[Formula: see text]h, the sample obtained possesses both the lowest temperature coefficient of dielectric constant ([Formula: see text]C between RT and [Formula: see text]C) and the highest Curie temperature ([Formula: see text]C at 100[Formula: see text]kHz). Moreover, at high temperatures, it exhibits a higher AC impedance than others. The calculating result based on the resistive constant-phase-element model (R-CPE) circuit model showed that the grain boundary of the 0.7BF–0.3BT ceramics contributes more resistance to the conductivity at high temperatures. In summary, the hydrothermal reaction proved to be a useful way that achieves the preparation of single-phase 0.7BF–0.3BT ceramics with improved electrical properties.

Synthesis of High‐Purity Monocalcium Phosphate Monohydrate from Crab Shell Waste

AbstractWaste crab shells (CS) have the potential to mineralize CO2, yielding precipitated calcium carbonate (PCC) powder feedstock for use in the synthesis of monocalcium phosphate monohydrate (MCPM) in an acidic condition by partial neutralization of phosphoric acid at 90 °C and varying times (30–120 min), followed by evaporation of the water at 100 °C. The PCC and MCPM products were analyzed using X‐ray powder diffraction, Fourier transform infrared spectroscopy, and the scanning electron microscopy/energy dispersive X‐ray method. After 120 min of stirring, the pure MCPM revealed uniform particle sizes from 1 to 3 μm. The presented MCPM synthesis using the PCC powder precursor may assist in developing a large‐scale MCPM industry while recycling a considerable quantity of CS waste.

High-Entropy Lead-Free Perovskite Bi0.2K0.2Ba0.2Sr0.2Ca0.2TiO3 Powders and Related Ceramics: Synthesis, Processing, and Electrical Properties.

A novel high-entropy perovskite powder with the composition Bi0.2K0.2Ba0.2Sr0.2Ca0.2TiO3 was successfully synthesized using a modified Pechini method. The precursor powder underwent characterization through Fourier Transform Infrared Spectroscopy and thermal analysis. The resultant Bi0.2K0.2Ba0.2Sr0.2Ca0.2TiO3 powder, obtained post-calcination at 900 °C, was further examined using a variety of techniques including X-ray diffraction, Raman spectroscopy, X-ray fluorescence, scanning electron microscopy, and transmission electron microscopy. Ceramic samples were fabricated by conventional sintering at various temperatures (900, 950, and 1000 °C). The structure, microstructure, and dielectric properties of these ceramics were subsequently analyzed and discussed. The ceramics exhibited a two-phase composition comprising cubic and tetragonal perovskites. The grain size was observed to increase from 35 to 50 nm, contingent on the sintering temperature. All ceramic samples demonstrated relaxor behavior with a dielectric maximum that became more flattened and shifted towards lower temperatures as the grain size decreased.