Search Results (317)

The construction industry’s growth is causing a surge in CO₂ emissions, driven by increased demand for concrete and other building materials. There is a growing demand for more sustainable building materials, including alkali-activated materials. This study investigates the impact of varying ratios of Na₂SiO₃ and NaOH on the mechanical properties and microstructure of metakaolin (MKW) and ceramic brick waste (CBW) based geopolymer binder. Geopolymer binder precursors were made of three main CBW/MKW ratios: 100/0%wt. (C100), 50/50%wt. (C50M50), and 0/100%wt. (M100). Alkaline activator solutions had three different Na₂SiO₃/NaOH ratios: 0.5, 1.0, and 2.0. The investigation into the geopolymer binder mechanical properties was conducted using a range of analytical methods, including compressive strength, scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR). The findings of the study indicate that the Na₂SiO₃/NaOH ratio alone is inadequate for evaluating geopolymer mechanical properties when different AS/P ratios are employed, given its influence on other parameters, such as the W/S ratio and the total Na₂O content. CBW-based geopolymer binders demonstrate limited capacity to attain substantial compressive strengths because they contain high amounts of unreacted CBW particles, as shown by XRD analysis. The incorporation of MKW precursor resulted in enhanced reactivity and intensified geopolymerization reaction. After the evaluation of all essential ratios, the most favorable Na₂SiO₃/NaOH ratio is 1.0. This determination was based on the highest strengths observed in designs that contained ≥50% of MKW precursor, attributed to predominance of goosecreekite and N-A-S-H gels, as evidenced by XRD and FT-IR analysis. Full article

Over more than half a century of using zirconia in technology and industry, researchers have faced several challenges related to the performance of this material. It is believed that some issues regarding the low performance of the zirconia ceramics can be solved by using a multidoping strategy. In this study, nanoparticles with the composition (1 − x)⸱ZrO₂ − x⸱MD (where MD—multi-dopant Y:Ce:Mg:Ca with cation relationship 1:1:1:1 and x = 0.05–0.25 mol. %) were synthesized using a hydrothermal method followed by annealing. XRD and Raman spectroscopy analyses demonstrated that in the concentration range of x = 0.10–0.25 mol.%, the only detectable phase in the synthesized samples was the tetragonal phase of zirconia. SEM analysis revealed that the size of the final particles ranged from 20 to 50 nm. It was demonstrated that using obtained nanoparticles as precursors for sintering leads to the formation of multiphase ceramics. The microhardness and biaxial flexural strength of the ceramic samples vary depending on the dopant concentration in the range of 600–1400 HV and 25–200 MPa respectively. Mechanical properties mostly depend on porosity and grain size in the sintered material. The study shows that the multidoping strategy has high potential to obtain new constructional ceramics and components for solid oxide fuel cells. Full article

The Na₂O-SrO-SiO₂ system shows promise in the development of glasses that can be transformed into electrically conductive glass ceramics. The conventional processing of such materials usually involves the synthesis of a parent glass, followed by a complex devitrification treatment. This study proposes a simplified approach based on the use of preceramic polymers, namely silicone resins combined with oxide fillers. These systems yield silicate-based ceramics through direct heat treatment, replicating the phase assembly of traditional glass ceramics with no need for prior glass melting. A printable formulation was developed by mixing a silicone resin with an acrylate-based photocurable resin, sodium nitrate and strontium carbonate. The resulting ‘suspension-emulsion’ was later shaped into monolithic components using digital light processing. After pyrolysis in nitrogen atmosphere, the components transformed into SrSiO₃ crystals embedded in a composite matrix, in turn composed of glass and turbostratic carbon (the latter specifically offered by the silicone polymer). This combination of crystalline silicates and carbon resulted in measurable electrical conductivity. This study confirms that silicone-derived systems can serve as effective precursors for conductive glass-ceramic analogues, providing an alternative to conventional methods with single-step processing. This approach enables structural shaping through 3D printing and the development of functional properties suitable for electronic or electrochemical applications. Full article

In the previous research that aimed to enhance the toughness and tribological properties of silicon nitride ceramics, a lignin precursor was added to the ceramic matrix, which achieved conversion through pyrolysis and sintering, resulting in a silicon nitride-based composite ceramic containing nitrogen-doped graphene quantum dots (N-GQDs). This composite material demonstrated excellent comprehensive mechanical properties and friction-wear performance. Based on the existing experimental results, the first-principles plane wave mode conservation pseudopotential method of density functional theory was adopted in this study to build a microscopic heterostructure model of Si₃N₄-based composite ceramics containing N-GQDs. Meanwhile, the surface energy of Si₃N₄ and the system energy of the N-GQDs@Si₃N₄ heterostructure were calculated. The calculation results showed that when the distance between N-GQDs and Si₃N₄ in the heterostructure was 2.3 Å, the structural energy was the smallest and the structure was the steadiest. This is consistent with the previous experimental results and further validates the coating mechanism of N-GQDs covering the Si₃N₄ column-shaped crystals. Simultaneously, based on the results of the previous experiments, the stress of the heterostructure composed of Si₃N₄ particles coated with different numbers of layers of nitrogen quantum dots was calculated to predict the optimal lignin doping amount. It was found that when the doping amount was between 1% and 2%, the best microstructure and mechanical properties were obtained. This paper provides a new method for studying the graphene quantum dot coating structure. Full article

Hydrogen energy offers high energy density and carbon-free combustion, making it a promising fuel for next-generation propulsion and power generation systems. Hydrogen offers approximately three times more energy per unit mass than natural gas, and its combustion yields only water as a byproduct, making it an exceptionally clean and efficient energy source. Materials used in hydrogen-fueled combustion engines must exhibit high thermal stability as well as resistance to corrosion caused by high-temperature water vapor. This study introduces a novel ceramic matrix composite (CMC) designed for such harsh environments. The composite is made of yttria-stabilized zirconia (YSZ) fiber-reinforced silicoboron carbonitride [Si(B)CN]. CMCs were fabricated via the polymer infiltration and pyrolysis (PIP) method. Multiple PIP cycles, which help to reduce the porosity of the composite and enhance its properties, were utilized for CMC fabrication. The Si(B)CN precursor formed an amorphous ceramic matrix, where the presence of boron effectively suppressed crystallization and enhanced oxidation resistance, offering superior performance than their counter part. Thermogravimetric analysis (TGA) confirmed negligible mass loss (≤3%) after 30 min at 1350 °C. The real-time ablation performance of the CMC sample was assessed using a hydrogen torch test. The material withstood a constant heat flux of 185 W/cm² for 10 min, resulting in a front-surface temperature of ~1400 °C and a rear-surface temperature near 700 °C. No delamination, burn-through, or erosion was observed. A temperature gradient of more than 700 °C between the front and back surfaces confirmed the material’s effective thermal insulation performance during the hydrogen torch test. Post-hydrogen torch test X-ray diffraction indicated enhanced crystallinity, suggesting a synergistic effect of the oxidation-resistant amorphous Si(B)CN matrix and the thermally stable crystalline YSZ fibers. These results highlight the potential of YSZ/Si(B)CN composites as high-performance materials for hydrogen combustion environments and aerospace thermal protection systems. Full article

Aluminum nitride (AlN) powder, a cornerstone material for advanced ceramics. This study examines the low-temperature formation of AlN crystals as well as their phase transformation by employing amorphous aluminum oxalate (AAO) as a novel precursor for carbothermal reduction, contrasting it with conventional aluminum hydroxide (Al(OH)₃). Through characterization using X-ray diffraction (XRD), scanning electron microscopy (SEM), High-Resolution Transmission Electron Microscope (HRTEM), ²⁷Al Magic-Angle Spinning Nuclear Magnetic Resonance (²⁷Al-MAS-NMR) energy-dispersive spectroscopy (EDS), and Fourier-transform infrared spectroscopy (FTIR), we unraveled the phase evolution pathways and the formation of AlN. Key findings reveal striking differences between the two precursors. When Al(OH)₃ was used, no AlN phase was detected at 1350 °C, and even at 1500 °C, the AlN obtained with significant residual alumina impurities. In contrast, the AAO precursor demonstrated exceptional efficiency: nano-sized α-Al₂O₃ formed at 1050 °C, followed by the emergence of AlN phases at 1200 °C, ultimately gaining the pure AlN at 1500 °C. The phase transformation sequence—Al(OH)₃ → γ-Al₂O₃ (950 °C) → (α-Al₂O₃ + δ-Al₂O₃) (1050 °C) → (AlN + α-Al₂O₃) (1200 °C~ 1350 °C) → AlN (≥1500 °C)—highlights the pivotal role of nano-sized α-Al₂O₃ in enabling low-temperature nano AlN synthesis. By leveraging the unique properties of AAO, we offer a transformative strategy for synthesizing nano-sized AlN powders, with profound implications for the ceramics industry. Full article

The chemical and structural similarity of calcium orthophosphates to hard tissues in the human body makes them suitable as biomaterials for bone implants, cements, injection systems, etc., for bone regeneration and reconstruction. Tetracalcium phosphate (Ca₄(PO₄)₂O, TTCP) is a promising component for such biomaterials due to its high calcium content and alkaline nature. The former makes it suitable for promoting mineralization, while the latter supports neutralization of the acidic environment, helping to prevent inflammation and improve the biocompatibility of the materials. However, it is the least used calcium orthophosphate due to the difficulties in its synthesis. This study examines the effect of high-energy mechanochemical activation on the phase evolution, particle morphology, and thermal behaviour of equimolar mixtures of Ca(OH)₂ and CaHPO₄, with the aim of optimizing precursor conditions for the synthesis of (TTCP)-rich ceramic materials. The results demonstrate that mechanochemical activation effectively induces structural disorder, promotes the formation of amorphous and nanocrystalline phases, and facilitates subsequent phase transitions upon calcination. The combined use of solid-state NMR, XRD, TEM, and thermal analysis provides a comprehensive understanding of the transformation pathways. Ultimately, 24 h of activation under the experimental conditions was identified as optimal for producing a precursor with a favorable phase composition for obtaining TTCP-rich ceramic materials after calcination at 1350 °C. Full article

SiC nanowires (SiC_nw), due to their excellent dielectric properties, are promising high-temperature absorbing materials. However, the mechanism of their high-temperature absorption still requires further research. Therefore, porous SiC_nw/Si₃N₄ and SiC/Si₃N₄ ceramics with different SiC phase morphologies were fabricated using a simple precursor impregnation and pyrolysis method. The Fe impurity content of the Si₃N₄ powder raw material significantly affects the generation of SiC nanowires. When SiC exists in the form of nanowires, the excellent conductivity brought by the conductive network of the nanowires causes a significant response of the material’s permittivity to temperature. When the test temperature is room temperature, SiC_nw/Si₃N₄ has excellent absorption performance with a minimum reflection loss of −29.75 dB at 2.16 mm and an effective absorption bandwidth of 3.72 GHz at 2.54 mm. As the test temperature increases to 300 °C, the effective absorption bandwidth of SiC_nw/Si₃N₄ covers the entire X-band. The porous SiC_nw/Si₃N₄ ceramics exhibit excellent electromagnetic wave absorption performance, demonstrating significant application potential for high-temperature environments. Full article

The recycling of glass presently poses several challenges, predominantly to the heterogeneous chemical compositions of various glass types, along with the waste glass particle size distribution, both of which critically influence the efficiency and feasibility of recycling operations. Numerous studies have elucidated the potential of converting non-recyclable glass waste into valuable materials thanks to the up-cycling strategies, including stoneware, glass wool fibres, glass foams, glass-ceramics, and geopolymers. Among the promising alternatives for improving waste valorisation of glass, alkali-activated materials (AAMs) emerge as a solution. Waste glasses can be employed both as aggregates and as precursors, with a focus on its application as the sole raw material for synthesis. This overview systematically explores the optimisation of precursor selection from a sustainability standpoint, specifically addressing the mild alkali activation process (<3 mol/L) of waste glasses. The molecular mechanisms governing the hardening process associated with this emerging class of materials are elucidated. Formulating sustainable approaches for the valorisation of glass waste is becoming increasingly critical in response to the rising quantities of non-recyclable glass and growing priority on circular economy principles. In addition, the paper highlights the innovative prospects of alkali-activated materials derived from waste glass, emphasising their emerging roles beyond conventional structural applications. Environmentally relevant applications for alkali-activated materials are reported, including the adsorption of dyes and heavy metals, immobilisation of nuclear waste, and an innovative technique for hardening as microwave-assisted processing. Full article

This study focuses on optimizing a sol–gel based electrodeposition–sintering process for producing yttria-stabilized zirconia (YSZ) ceramic coatings on stainless steel substrates. Four key process variables—precursor concentration, current density, sintering time, and temperature—were evaluated in terms of two response variables: R (electrodeposition yield) and S (sintering yield). A fractional factorial design was used to reduce the number of experiments while enabling robust statistical modeling. Multiple linear regression analysis revealed that precursor concentration and current density were the most influential factors for both R and S, whereas sintering time and temperature had a lesser effect. Under central conditions (42.9 g·L⁻¹, 1.5 A·cm², 500 °C, 20 min), coatings exhibited yields of ~3.9 mg·cm² and superior morphological uniformity. Higher current density (3 A·cm²) increased R to 6.9 mg·cm² but induced porosity and cracking. Compared to conventional sol–gel derived coatings, the proposed methodology enables a more controlled microstructure with a trade-off between mass deposition and structural integrity. This predictive, statistically validated approach facilitates the optimization of electrodeposition parameters to obtain defect-minimized ceramic coatings, particularly suited for protective and thermal barrier applications in demanding environments. Full article

This study addresses the use of porcelain polishing waste as a pyro-expansive agent in clay-based formulations for the production of lightweight aggregates, aiming to reduce the consumption of natural resources and mitigate environmental impacts. In line with circular economy principles and sustainable construction goals, this study investigates the potential use of porcelain polishing waste as a pyro-expansive agent in clay-based formulations for producing sustainable lightweight aggregates. Using the Taguchi method and ANOVA, the effects of key processing parameters were evaluated. The results demonstrated a broad range of volumetric changes, from shrinkage of 40.84% to expansion of 91.69%, depending on the formulation and processing conditions. The aggregates exhibited specific mass values ranging from 0.99 g/cm³ to 2.36 g/cm³, water absorption up to 3.29%, and mechanical strength from 4.57 MPa to 39.87 MPa. Notably, nine of the sixteen experimental conditions met the technical standards for classification as LWA, indicating suitability for applications in high-strength, structural, and non-structural lightweight concretes, as well as lightweight mortars. The performance of these materials was directly linked to the chemical and mineralogical characteristics of the precursors and the proportion of pyro-expansive waste used. Overall, the findings suggest that 50% of the produced aggregates are viable for high-performance concrete applications, offering an environmentally responsible alternative to virgin raw materials and contributing to sustainable waste valorization in the ceramic and construction industries. 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

Cement-based building materials usually exhibit weak flexural behavior under high temperature or fire conditions. This paper develops a novel geopolymer with enhanced residual flexural strength, incorporating fly ash/metakaolin precursors and corundum aggregates based on our previous study, and further improves flexural performance using hybrid fibers. The flexural load–deflection response, strength, deformation capacity, toughness and microstructure are investigated by a thermal exposure test, bending test and microstructure observation. The results indicate that the plain geopolymer exhibits a continuously increasing flexural strength from 10 MPa at 20 °C to 25.9 MPa after 1000 °C exposure, attributed to thermally induced further geopolymerization and ceramic-like crystalline phase formation. Incorporating 5% wollastonite fibers results in slightly increased initial and residual flexural strength but comparable peak deflection, toughness and brittle failure. The binary 5% wollastonite and 1% basalt fibers in geopolymer obviously improve residual flexural strength exposed to 400–800 °C. The steel fibers show remarkable reinforcement on flexural behavior at 20–800 °C exposure; however, excessive steel fiber content such as 2% weakens flexural properties after 1000 °C exposure due to severe oxidation deterioration and thermal incompatibility. The wollastonite/basalt/steel fibers exhibit a positive synergistic effect on flexural strength and toughness of geopolymers at 20–600 °C. Full article

To address the poor thermal shock resistance and high brittleness of traditional ceramic tools, a novel Si₃N₄/Sc₂W₃O₁₂ (SNS) composite ceramic material was developed via in situ synthesis using WO₃ and Sc₂O₃ as precursors and consolidated by spark plasma sintering. Sc₂W₃O₁₂ with negative thermal expansion was introduced to compensate for matrix shrinkage and modulate interfacial stress. The effects of varying Sc₂W₃O₁₂ content on thermal expansion, residual stress, microstructure, and mechanical properties were systematically investigated. Among the compositions, SNS3 (12 wt.% Sc₂W₃O₁₂) exhibited the best overall performance: relative density of 98.8 ± 0.2%, flexural strength of 712.4 ± 30 MPa, fracture toughness of 7.5 ± 0.3 MPa·m^1/2, Vickers hardness of 16.3 ± 0.3 GPa, and an average thermal expansion coefficient of 2.81 × 10⁻⁶·K⁻¹. The formation of a spherical chain-like Sc-W-O phase at the grain boundaries created a “hard core–soft shell” interface that enhanced crack resistance and stress buffering. Cutting tests showed that the SNS3 tool reduced workpiece surface roughness by 32.91% and achieved a cutting distance of 9500 m. These results validate the potential of this novel multiphase ceramic system as a promising candidate for high-performance and thermally stable ceramic cutting tools. Full article

A ceramic–metal composite was synthesized using sol–gel and electrospinning methods to serve as a SERS substrate. The precursors used were tetraethyl orthosilicate, aluminum nitrate, and zirconium, and polyvinylpyrrolidone was added to electrospun nonwoven fibrous membranes. The membranes were sintered, decorated with silver nanoparticles. The enhancement substrates were made of fibers of cylindric morphology with an average diameter of approximately 190 nm, a smooth surface, and 9 nm spherical particles decorating the surface of the fibers. The enhancement capacity of the substrates was tested using pyridine, methyl orange, methylene blue, crystal violet, and Eriochrome black T at different concentrations with Raman spectroscopy to determine whether the size and complexity of the analyte has an impact on the enhancement capacity. Enhancement factors of 2.53 × 10², 3.06 × 10¹, 2.97 × 10³, 4.66 × 10³, and 1.45 × 10³ times were obtained for the signal of pyridine, methyl orange, methylene blue, crystal violet, and Eriochrome black T at concentrations of 1 nM. Full article