Search Results (197)

Bi₆Fe₂Ti₃O₁₈ (BFTO) ceramics were synthesized via a solid-state reaction route using stoichiometric amounts of Bi₂O₃, TiO₂, and Fe₂O₃ powders. A thermal analysis of the powder mixture was conducted to optimize the heat treatment parameters. Energy-dispersive X-ray spectroscopy (EDS) confirmed the conservation of the chemical composition following calcination. Final densification was achieved through hot pressing. The crystal structure of the sintered samples, examined via X-ray diffraction at room temperature, revealed a tetragonal symmetry for BFTO ceramics sintered at 850 °C. Electron backscatter diffraction (EBSD) provided detailed insight into the crystallographic orientation and microstructure. Broadband dielectric spectroscopy (BBDS) was employed to investigate the dielectric response of BFTO ceramics over a frequency range of 10 mHz to 10 MHz and a temperature range of −30 °C to +200 °C. The temperature dependence of the relative permittivity (ε_r) and dielectric loss tangent (tan δ) were measured within a frequency range of 100 kHz to 900 kHz and a temperature range of 25 °C to 570 °C. The impedance data obtained from the BBDS measurements were validated using the Kramers–Kronig test and modeled using the Kohlrausch–Williams–Watts (KWW) function. The stretching parameter (β) ranged from ~0.72 to 0.82 in the impedance formalism within the temperature range from 200 °C to 20 °C. Full article

The precursor-derived ceramic route is recognized as an advanced and efficient technique for fabricating ceramic matrix composites, particularly suitable for the development and microstructural tailoring of continuous fiber-reinforced ceramic matrix composites. In this work, octamethylcyclotetrasiloxane and tetravinylcyclotetrasiloxane were employed as monomers to synthesize a branched siloxane via ring-opening polymerization. A subsequent hydrosilylation reaction led to the formation of polyvinylsiloxane with a three-dimensional crosslinked structure. The precursor exhibited excellent fluidity, adjustable viscosity, and superior thermosetting characteristics, enabling efficient impregnation and densification of reinforcements through the polymer infiltration and pyrolysis process. Upon pyrolysis, the polyvinylsiloxane gradually converted from an organic polymer to an amorphous inorganic ceramic phase, yielding silicon oxycarbide ceramics with a high ceramic yield of 81.3%. Elemental analysis indicated that the resulting ceramic mainly comprised silicon and oxygen, with a low carbon content. Furthermore, the material demonstrated a stable dielectric constant (~2.5) and low dielectric loss (<0.01), which are beneficial for enhanced thermal stability and dielectric performance. These findings offer a promising precursor system and process reference for the low-cost production of high-performance, multifunctional ceramic matrix composites with strong potential for engineering applications. Full article

Textured Si₃N₄/BN composite ceramics were successfully fabricated using two-step sintering, combining pseudo-hot isostatic pressing (PHIP) and gas pressure sintering. The grain size of h-BN platelets had a significant influence on densification and mechanical and thermal properties. With an increase in h-BN grain size, the volume density of the composite ceramics gradually decreased, while flexural strength gradually increased. Meanwhile, larger h-BN platelets were more likely to trigger toughening mechanisms like large-angle deflection and greatly increase fracture toughness. Through proper selection of h-BN grain size, textured ceramics, with the addition of h-BN platelets of 1–2 μm, showed high thermal conductivity (∼92 W∙m⁻¹∙K⁻¹) and reliable mechanical properties (∼540 MPa, ∼7.5 MPa∙m^1/2, ∼11.1 GPa). Therefore, texture control is an effective means of improving the overall performance of ceramic materials. Novel textured composite ceramics thus have great potential in large-scale fabrication and directional heat dissipation applications. Full article

The sustainable valorization of electrolytic manganese residue (EMR) and fly ash (FA) presents critical environmental challenges. This study systematically investigates the performance optimization of EMR-FA ceramic composites through the coordinated regulation of raw material ratios, sintering temperatures, and additive effects. While the composite with 85 g FA exhibits the highest mechanical strength, lowest porosity, and minimal water absorption, the formulation consisting of 45 wt% EMR, 40 wt% FA, and 15 wt% kaolin is identified as a balanced composition that achieves an effective compromise between mechanical performance and solid waste utilization efficiency. Sintering temperature studies revealed temperature-dependent property enhancement, with controlled sintering at 1150 °C preventing the over-firing phenomena observed at 1200 °C while promoting phase evolution. XRD-SEM analyses confirmed accelerated anorthite formation and the morphological transformations of FA spherical particles under thermal activation. Additive engineering demonstrated that 8 wt% CaO addition enhanced structural densification through hydrogrossular crystallization, whereas Na₂SiO₃ induced sodium-rich calcium silicate phases that suppressed anorthite development. Contrastingly, ZrO₂ facilitated zircon nucleation, while TiO₂ enabled progressive performance enhancement through amorphous phase modification. This work establishes fundamental phase–structure–property relationships and provides actionable engineering parameters for sustainable ceramic production from industrial solid wastes. Full article

The improvement of densification and fracture toughness in high-entropy ceramics is important to realizing their practical applications. In this study, SiC whiskers and metal Ni additions were incorporated to solve these problems of high-entropy boride ceramics. The influence of sintering temperatures (1450–1650 °C) on the densification, microstructure, hardness, fracture toughness, and bending strength of (M_0.2Ti_0.2Ta_0.2V_0.2Nb_0.2)B₂-SiC_w-Ni (M=Hf, Zr, or Cr) composites prepared by hot-pressing technology were studied. Results showed that when SiC whiskers and metal Ni additions were used as additives, increasing sintering temperatures from 1450 to 1600 °C promoted the densification of high-entropy boride ceramics. This was mainly attributed to the high sintering driving force. However, when the temperature further increased to 1650 °C, their densification behavior decreased. At a sintering temperature of 1600 °C, these high-entropy borides ceramics all had the highest densification behavior, leading to their high hardness and fracture toughness. The highest relative density was 96.3%, the highest hardness was 22.02 GPa, and the highest fracture toughness was 13.25 MPa·m^1/2, which was improved by the co-function of SiC whiskers and plastic metal Ni. Meanwhile, in the adopted sintering temperature range of 1450 to 1650 °C, the highest bending strength at room temperature of these high-entropy boride ceramics could reach 320.8 MPa. Therefore, this research offers an effective densification, strengthening, and toughening method for high-entropy boride composites at a low sintering temperature. Full article

In this investigation, TiB₂–TiC composite powders, synthesized via the boron/carbon thermal reduction process, were employed as precursor materials. SiC, serving as the tertiary constituent, was incorporated to fabricate TiB₂–TiC–SiC composite ceramics utilizing spark plasma sintering technology. The present study initially elucidates the densification mechanisms and investigates the influence of sintering temperature on the densification behavior, microstructural evolution, and mechanical properties of the resultant ceramics. The experimental findings reveal that the sintering process of TiB₂–TiC–SiC ceramics exhibits characteristics consistent with solid-phase sintering. As the sintering temperature escalates, both the relative density and mechanical properties of the ceramics initially improve, reaching a maximum at an optimal sintering temperature of 1900 °C, before subsequently declining. Microstructural examinations conducted at this optimal temperature indicate a homogeneous distribution of the two primary phases, with no evidence of excessive grain growth. Furthermore, this research explores the effects of SiC addition on the mechanical performance and oxidation resistance of TiB₂–TiC–SiC composite ceramics. The results demonstrate that the incorporation of SiC effectively suppresses grain growth and promotes the formation of rod-like TiB₂ microstructures, thereby enhancing the mechanical attributes of the ceramics. Additionally, the addition of SiC significantly improves the oxidation resistance of the composite ceramics compared to their TiB₂–TiC binary counterparts Full article

Microwave dielectric ceramics are indispensable in modern communication technologies, playing a pivotal role in components such as filters, oscillators, and antennas. Among these materials, ZnAl₂O₄ ceramics have garnered attention for their excellent quality factor (Q × f) and low dielectric constant (ε_r). However, their high sintering temperature (~1650 °C) limits practical applications. This study investigates ZnAl_2-x(Zn_0.5Si_0.5)_xO₄ (ZAZS) (x = 0.1–0.9) ceramics, where [Zn_0.5Si_0.5]³⁺ substitutes Al³⁺, to reduce sintering temperature while maintaining high-performance microwave dielectric properties. ZAZS ceramics were synthesized via the solid-state reaction method and characterized for their structural, morphological, and dielectric properties. X-ray diffraction analysis confirmed the formation of a single-phase solid solution up to x = 0.8, with minor secondary phases appearing at x = 0.9. The substitution increased lattice parameters and enhanced material densification, as observed through SEM and relative density calculations. Microwave dielectric measurements showed that ZAZS ceramics achieved a maximum Q × f of 20,200 GHz and a τ_f value reduced to −62 ppm/°C at x = 0.8, while ε_r decreased from 7.90 to 6.98. Bond-valence calculations reveal that the reduction of the average Al/Zn/Si–O bond valence weakens octahedral rigidity, systematically tuning τ_f toward zero. These results demonstrate that ZAZS ceramics, with a reduced sintering temperature of 1400 °C, exhibit excellent potential for application in low-loss microwave devices. Full article

Illitic clays are one of the most important materials used in the ceramic industry. Carbonates support the densification and the sintering of ceramics. Five mixtures of illitic clay with calcite were prepared aiming for the crystallization of anorthite ceramics. The stoichiometric ratio of anorthite crystallization was determined at 21.6 wt.% of calcite content. To reveal the effect of calcite on the crystallization processes, two more mixtures were prepared below the stoichiometric composition (17.6 wt.% and 19.6 wt.%) and two more mixtures above the ideal composition (23.6 wt.% and 25.6 wt.%). X-ray diffraction revealed that gehlenite and Ca-feldspar were formed, which are the intermediate phases in anorthite crystallization. However, due to the low purity of illitic clay and the low firing temperature, no anorthite formation was observed. The influence of calcite content on Young’s modulus was negligible. However, a clear effect on the open porosity was revealed. Full article

The effect of induction heating on alumina ceramics and alumina ceramic composites based on α-Al₂O₃ nanopowders (additives: SiC, Si₃N₄, SiO₂, ZrO₂) has been examined. Various factors such as the structure, grain size, distribution of elements, hardness, fracture toughness, and wear rate of hot-pressed ceramic materials were assessed. Despite achieving improved densification of alumina ceramics at a higher temperature of 1720 °C, there is a consistent trend toward a decline in hardness and fracture toughness. Heating at lower temperatures of 1300–1500 °C results in the development of a strengthened surface layer with a fine-grained structure enriched with carbon. Therefore, the wear rate behavior of such ceramics differs from the behavior of samples made at higher temperatures of 1600–1720 °C. This fact indicates the presence of a non-thermal microwave effect of induction heating. The incorporation of additives to alumina leads to the formation of novel structures with altered crack propagation patterns. The optimal ceramic composite, containing 5 wt. % SiC, displayed superior hardness and the lowest wear rate when compared to pure alumina ceramics. Across all investigated composites, a short dwell time at 1700 °C results in an enhancement of the mechanical properties. Full article

Proton-conducting ceramics have gained significant attention in various applications. Yttrium-doped barium cerium zirconate (BaCe_xZr_1−x−yY_yO_3–δ) is the state-of-the-art proton-conducting electrolyte but poses a major challenge because of its high sintering temperature. Sintering aids have been found to substantially reduce the sintering temperature of BaCe_xZr_1−x−yY_yO_3–δ. This work evaluates, for the first time, the impact of NiO and ZnO addition in three different loadings (1, 3, 5 mol%), via wet mechanical mixing, on the sintering and electrical properties of a low cerium-containing composition, BaCe_0.2Zr_0.7Y_0.1O_3–δ (BCZY). The sintering temperature remarkably dropped from 1600 °C (for pure BCZY) to 1350 °C (for NiOBCZY and ZnOBCZY) while achieving > 95% densification. In general, ZnO gave higher densification than NiO, the highest being 99% for 5 mol% ZnOBCZY. Dilatometric studies revealed that ZnOBCZY attained complete shrinkage at temperatures lower than NiOBCZY. Up to 650 °C, ZnO showed higher conductivity compared to NiO for the same loading, mostly due to a higher extent of Zn incorporation inside the BCZY lattice as seen from the BCZY peak shift to a lower Bragg’s angle in X-ray diffractograms, and the bigger grain sizes of ZnO samples compared to NiO captured in scanning electron microscopy. At any temperature, the variation in conductivity as a function of sintering aid concentration followed the orders 1 mol% > 3 mol% > 5 mol% (for ZnO) and 1 mol% < 3 mol%~5 mol% (for NiO). This difference in conductivity trends has been attributed to the fact that Zn fully dissolves into the BCZY matrix, unlike NiO which mostly accumulates at the grain boundaries. At 600 °C, 1 mol% ZnOBCZY showed the highest conductivity of 5.02 mS/cm, which is, by far, higher than what has been reported in the literature for a Ce/Zr molar ratio <1. This makes ZnO a better sintering aid than NiO (in the range of 1 to 5 mol% addition) in terms of higher densification at a sintering temperature as low as 1350 °C, and higher conductivity. Full article

Lithium hydride (LiH) is one promising material for nuclear reactor shielding due to its high hydrogen content, but its poor mechanical strength and thermal conductivity pose challenges for fabricating large, crack-free ceramic components via conventional sintering. This study explores microwave sintering as a potential solution to enhance heating uniformity and reduce thermal stress during densification of bulk LiH ceramics. Using implicit function and level set methods, we numerically simulated the microwave field distribution and thermal response in both stationary and rotating samples. The results show that rotational heating improves temperature uniformity by up to 12.9% for specific samples, although uniform temperature control remains difficult through rotation alone. To mitigate stress accumulation from thermal gradients, we propose a cyclic sintering–resting strategy, which leverages LiH’s tensile strength–temperature envelope to guide safe and efficient processing. This strategy successfully reduced total sintering time from several days to 1.63 h without inducing cracks. Our findings offer practical insights into optimizing microwave sintering parameters for large-scale LiH ceramic production and contribute to enabling its application in advanced nuclear shielding systems. Full article

Nano-titanium dioxide ceramic coatings exhibit excellent wear resistance, corrosion resistance, and self-cleaning properties, showing great potential as multifunctional protective materials. This study proposes a synergistic reinforcement strategy by encapsulating micron-sized Al₂O₃ particles with nano-TiO₂. A core-shell structured nanocomposite coating composed of 65 wt% nano-TiO₂ encapsulating 30 wt% micron-Al₂O₃ was precisely designed and fabricated via a slurry dip-coating method on Q235 steel substrates. The microstructure and surface morphology of the coatings were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD). Comprehensive performance evaluations including densification, adhesion strength, wear resistance, and thermal shock resistance were conducted. Optimal coating properties were achieved under the conditions of a binder-to-solvent ratio of 1:15 (g/mL), a heating rate of 2 °C/min, and a sintering temperature of 400 °C. XRD analysis confirmed the formation of multiple crystalline phases during the 400 °C curing process, including titanium pyrophosphate (TiP₂O₇), aluminum phosphate (AlPO₄), copper aluminate (Cu(AlO₂)₂), and a unique titanium phosphate phase (Ti₃(PO₄)₄) exclusive to the 2 °C/min heating rate. Adhesion strength tests revealed that the coating sintered at 2 °C/min exhibited superior interfacial bonding strength and outstanding performance in wear resistance, hardness, and thermal shock resistance. The incorporation of nano-TiO₂ into the 30 wt% Al₂O₃ matrix significantly enhanced the mechanical properties of the composite coating. Mechanistic studies indicated that the bonding between the nanocomposite coating and the metal substrate is primarily achieved through mechanical interlocking, forming a robust physical interface. These findings provide theoretical guidance for optimizing the fabrication process of metal-based ceramic coatings and expanding their engineering applications in various industries. Full article

Silicon carbide (SiC) materials have demonstrated promising application prospects in modern manufacturing due to their outstanding physical and chemical properties. With its process flexibility and formation feasibility, binder jetting 3D printing technology has become a crucial technical approach to meet the demand for mass production of complex, high-performance SiC components. Addressing the technical challenges of traditional manufacturing techniques in achieving high-quality, complex-shaped SiC components, this paper systematically reviews the application of binder jetting 3D printing technology in fabricating high-quality SiC-based ceramic components, with a particular focus on the regulation of key process parameters affecting SiC green body formation quality and the optimization of post-densification processes. Firstly, this paper elaborates on the powder pretreatment, green part formation process, and post-processing chain involved in this technology, establishes an evaluation index system for formation quality, and provides research directions for rapid prototyping of SiC powders. Secondly, it provides an in-depth analysis of the influence patterns of jetting parameters (e.g., jetting conditions, powder characteristics, binder properties) and various post-processing techniques on the quality of SiC-based components, along with optimization methods to enhance the dimensional accuracy and mechanical properties of 3D-printed SiC components. Furthermore, this paper systematically summarizes advanced characterization methods for evaluating formation quality and demonstrates the technology’s application potential across multiple industrial fields through representative engineering cases. Finally, it predicts the future development trends of this technology and discusses potential application expansion directions and key scientific issues in current research, aiming to provide theoretical references for promoting in-depth development of this technology. Full article

This study investigates the effect of duo-ceramic zirconia and silicon nitride (ZrO₂-Si₃N₄) particles and their reinforcement proficiencies on a Ti6Al4V alloy, consolidated using the spark plasma sintering (SPS) technique. The selected sintering parameters are, viz., 900 °C temperature, 50 MPa pressure, 10 min of holding time, and 100 °C/min of sintering rate. SEM/EDS and XRD equipment were used to disclose the microstructural evolution and phase identification of created composites. The mechanical characteristics of the resulting composites were determined using the nanoindentation technique. All consolidated sintered composites showed excellent densification, with sample relative densities reaching 96.65%. Significant improvements were also made in their nanomechanical characteristics; among the composite samples with different volume fractions, the ceramics with the lowest volume percentage had the best mechanical characteristics, whereas the sintered samples with the highest ceramic volume percentage showed a decrease in mechanical proficiencies and relative density. Composite S1, with the lowest volume fraction of the duo-ceramic particles, was seen to have a significant mechanical property improvement better than other composites, S2 and S3, in terms of measured Vickers microhardness, elastic modulus, and nano hardness values at a sintering temperature of 900 °C. Consequentially, composite specimens S2 and S3’s mechanical characteristics and relative densities dropped as the volume fractions of the duo-ceramic particles increased. Full article

This paper systematically investigated the influence of sintering atmospheres, vacuum, and oxygen, on the microstructure and optical properties of Y₂O₃ ceramics. Compared with vacuum sintering, sintering in flowing oxygen atmosphere can effectively inhibit the grain growth of Y₂O₃ ceramics at the final stage of sintering and improve the uniformity of microstructure. After hot isostatic pressing, the samples pre-sintered at oxygen atmosphere showed good in-line transmittance from a visible-to-mid-infrared wavelength range (0.4–6.0 μm) except in the range of 2.8–4.1 μm. Spectral analysis showed that an obvious broadband absorption peak (2.8–4.1 μm) of characteristic hydroxyl groups is detected in the above samples. However, before densification, a low-temperature heat treatment at 600 °C under vacuum can effectively diminish the hydroxyl groups in Y₂O₃ ceramics. However, laser experiments in the ~1 μm wavelength range showed that although the Yb:Y₂O₃ ceramic carrying hydroxyl had obvious absorption in the 2.8–4.1 μm range, it had little effect on its laser oscillation in the ~1 μm wavelength. Yb:Y₂O₃ ceramics pre-sintered in an oxygen atmosphere at 1460 °C followed by hot isostatic pressing at 1440 °C achieved 12.85 W continuous laser output at room temperature, with a laser slope efficiency of 84.4%. Full article