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Purpose: To compare the translucency parameters and masking abilities of different monolithic CAD/CAM ceramics placed on different-colored substructures. Materials and Methods: Square-shaped specimens (12 × 12 × 1.5 mm) were prepared from feldspathic (C), leucite (EMP), lithium disilicate (e.max), zirconiareinforced lithium silicate (VS), resin nanoceramic (LU), polymer-infiltrated ceramic (VE), hybrid nanoceramic (GC), monolithic zirconia (TZI), and composite resin (TC) blocks (n = 10 per material). After mechanical polishing, the translucency parameter (TP) was calculated. Then, each ceramic specimen was measured on eight substructures, and the color difference between ND2 and each substrate was calculated with the CIEDE2000 formula. TP values were analyzed with one-way ANOVA and Games-Howell tests, and the color differences indicating masking ability were analyzed with two-way ANOVA and Tukey HSD tests. Results: The highest TP was observed in TC, followed by LU, EMP, C,GC, e.max, VS, VE, and TZI. The E00 color difference values of TZI, VS, and VE on all abutment colors, except for ND9, were below the acceptable threshold value. Conclusions: All monolithic ceramic materials used in the study masked the ND1 and ND3 substrates. The ND9, representing severely discolored or devitalized preparations, could not be masked by any monolithic CAD/CAM ceramics used in the study. [ABSTRACT FROM AUTHOR]

Purpose: To compare the masking ability of monolithic CAD/CAM veneers placed over different resin cement shades and substrate colors. Materials and Methods: Veneers were milled from four different monolithic CAD/CAM restorative materials: feldspathic ceramic (VMII), lithium disilicate ceramic (Emax CAD), zirconiareinforced lithium silicate ceramic (VS), and high-translucency zirconia ceramic (YZ-XT). Veneers were luted on natural tooth-colored (ND1) or discolored substrates (ND3 or ND5) using two different resin cement shades (opaque white or translucent). Each CAD/CAM material, resin cement shade, and substrate combination comprised 9 sample veneers (N = 216). Color parameters were obtained using a dental spectrophotometer before and after luting. Color differences (E00) were calculated using CIEDE2000 formula and compared to perceptibility (P = .81 E00 units) and acceptability (AT = 1.77 E00 units) visual thresholds. Color variation data were statistically analyzed using Kruskal-Wallis and Mann-Whitney U tests with Bonferroni-Holm correction (a = .05). Results: The highest E00 value was obtained in the VMII group placed over a discolored substrate, followed by the Emax CAD, YZ-XT, and VS groups. The effect of material types on E00 values was significantly observed when the veneers were luted on discolored substrates using translucent resin cement (P < .05). Conclusions: Restorative material type, substrate color, and resin cement shade affect the masking ability of monolithic CAD/CAM laminate veneers. [ABSTRACT FROM AUTHOR]

Purpose: To evaluate inlay and onlay marginal adapta2on of two different ceramic materials using two intracoronal prepara2on designs. Materials and Methods: An examina2on of the marginal adap2on of two materials--lithium disilicate (LD; IPS e.max CAD) and polymer infiltrated ceramic network material (PICN; Vita Enamic)--and two prepara2on designs, where D1 represents MOD inlay prepara2on with no cusp reduc2on and for D2, in addi2on to the basic MOD prepara2on, the buccal cusps (func2onal cusps) were reduced by 1.5 mm. Four sub-groups (LD-D1, LD-D2, PICN-D1, PICN-D2) were conducted. In total, 40 (n = 40) mandibular molars were used. A stereomicroscope was used to assess the marginal gap before, aWer cementa2on and aWer thermocycling. Values were calculated for the mean, median, SD, minimum, maximum, and 95% CI. Pairwise comparisons using Tukey post-hoc test were performed following an ANOVA significance of P = .05. Results: The results revealed that lithium disilicate showed sta2s2cally significantly higher mean gap distance than PICN material (61 µm to 99 µm). Pairwise comparisons showed that D2 design has sta2s2cally significant higher mean gap values than D1. Conclusions: Both LD and PICN material provided marginal adapta2on within clinical accepted range. PICN material restora2ons provided beer fit than lithium disilicate restora2ons. Cusp coverage has a greater marginal gap compared to conven2onal prepara2on. [ABSTRACT FROM AUTHOR]

Ceramic materials are widely used in armor or protective structures, providing weight saving at equivalent performance in comparison to their steel counterparts. Plate-impact experiments are commonly used to investigate the dynamic behavior of ceramics under compressive loading. Using the particle velocity measured at the back of the target, some mechanical properties such as the Hugoniot elastic limit (HEL) as well as the Hugoniot curve of the material can be deduced. Nevertheless, these tests do not provide a direct measurement of the plastic hardening (post-HEL) behavior of the target. In the present work, an experimental shockless plate-impact configuration was developed and implemented to conduct a Lagrangian analysis. This configuration relies on the use of a wavy-machined flyer plate impacting a target made of a buffer, two ceramic plates of different thicknesses, and two window plates as backing. First, the use of wavy flyer plates to generate a loading ramp was validated by considering the impact of the wavy-machined flyer plate against a target, both made of 316L steel. A numerical analysis of this test was developed to confirm the pulse-shaping effect observed experimentally. Next, a ceramic, F99.7 alumina was subjected to the shockless plate impact test in Lagrangian configuration considering the same steel as a buffer and flyer plate material. These tests coupled with Lagrangian analysis enable the curve of axial-stress vs axial-strain beyond the isentropic elastic limit (IEL) to be deduced. The experimental data allow identifying the parameters of an elastoplastic with strain-hardening model to describe the behavior of the tested alumina. [ABSTRACT FROM AUTHOR]

Purpose: To assess the clinical performance of CAD/CAM laminate veneers placed by a single operator and systematically evaluated for up to 10 years. Materials and Methods: A total of 197 laminate veneers fabricated using either feldspathic ceramics (VMII) or lithium disilicate ceramics (EmaxCAD) were followed up to 10 years in 32 patients. Technical, esthetic, and biologic findings of each restoration were evaluated using modified United States Public Health Service criteria. The survival and complication rates were assessed using Kaplan-Meier survival analysis and compared using log-rank test. Statistical significance was set at P < .05. Results: The estimated Kaplan-Meier survival rate was 91.9% after the mean observation period. According to the ceramic system used, the estimated Kaplan-Meier survival rate amounted to 92.7% for EmaxCAD and 89.1% for VMII. Survival rates were significantly affected by the location of veneer according to log-rank test (P < .05). A range of survival rates between 83.3% and 98.6% were observed based on the location of veneer. Conclusions: CAD/CAM laminate veneers milled from feldspathic or lithium disilicate ceramics have comparable long-term survival rates. Oral positioning affects the survival of veneers. Veneers of incisors have higher survival rates than the veneers of maxillary canines and premolars. [ABSTRACT FROM AUTHOR]

In this study, the influence of ceramic shield characteristics, including thickness and geometry, on the transmission spectrum and electron density measurements of a ceramic shield cutoff probe (CSC) was investigated to measure high-density or process plasma. Through electromagnetic simulations and circuit modeling, we examined the measurement characteristics of the CSC based on different ceramic shield geometries. When the ceramic shield is sufficiently thin, it does not affect the CSC wave transmission characteristics. However, for a thick ceramic shield, a cutoff frequency shift of up to 3% toward the lower side can occur. This shift is attributed to the electrical properties of the ceramic material, which can function as a parasitic capacitor. In addition, when fabricating a CSC, depending on the shape of the ceramic shield or the method used to couple it with the CSC body, a cutoff frequency shift can occur toward the lower side. The simulation results were validated through experiments, revealing a cutoff frequency shift toward the lower side of up to 18.0% in the simulations and up to 11.6% in the experiments. The findings of this study could assist in high-density or processing plasma measurements using cutoff probes. [ABSTRACT FROM AUTHOR]

Extensive experimental and computational studies have demonstrated outstanding physical and chemical properties of the novel materials of compositionally complex carbides (CCCs), enabling their promising applications in advanced fission and fusion energy systems. This perspective provides a comprehensive overview of radiation damage behavior reported in the literature to understand the fundamental mechanisms related to the impact of multi-principal metal components on phase stability, irradiation-induced defect clusters, irradiation hardening, and thermal conductivity of compositionally complex carbides. Several future research directions are recommended to critically evaluate the feasibility of designing and developing new ceramic materials for extreme environments using the transformative "multi-principal component" concept. Compared to the existing materials for nuclear applications including stainless steels, nickel alloys, ZrC, SiC, and potentially high-entropy alloys, as well as certain other compositionally complex ceramic families. CCCs appear to be more resistant to amorphization, growth of irradiation defect clusters, and void swelling. [ABSTRACT FROM AUTHOR]

A series of Sr0.7Ba0.3Nb2O6−δ/x wt. % Ti (x = 1, 3, 5, and 10) composite ceramic thermoelectric materials were prepared, and the mechanism for improving their thermoelectric properties was explored. The experimental results demonstrate that nano-additive titanium powder undergoes oxidation to form TiO2 during sintering. However, under annealing in a reducing atmosphere, oxidation reactions further deplete the lattice oxygen, leading to an increased generation of oxygen vacancies and enhanced carrier concentration, ultimately leading to successful resistivity reduction. The samples consistently exhibit low thermal conductivity values below 2.0 W m−1 K−1 due to crystal defects, complex structure, and phonon scattering at the grain boundaries. The sample doped with 5 wt. %. Ti exhibits the lowest resistivity and highest PF value (409.3 μW/m K2 at 1073 K). Consequently, the figure of merit of Sr0.7Ba0.3Nb2O6−δ with 5 wt. % Ti attains its maximum value of 0.30 at 1073 K, representing a 50% increase compared to that of the undoped sample Sr0.7Ba0.3Nb2O6−δ (0.20 at 1073 K). [ABSTRACT FROM AUTHOR]

Purpose: To investigate the influence of immediate dentin sealing (IDS) vs delayed dentin sealing (DDS) on the marginal gaps of machinable monolithic zirconia vs pressable lithium disilicate laminate veneers.Materials and Methods: A total of 40 maxillary lateral incisors were used and received butt-joint laminate veneer preparation. The samples were divided into two groups (n = 20 each) according to ceramic material: pressable lithium disilicate ceramic (PLD) was used in the first group, and machinable monolithic zirconia (MMZ) was used in the second. Each group was then divided into two subgroups according to the bonding protocol: IDS was employed in one, and DDS in the other (n = 10 each). The marginal gap widths were measured using digital microscopy and statistically analyzed.Results: The smallest marginal gaps were observed in MMZ-DDS (57.2 ± 8.4 μm), followed by PLD-DDS (62.4 ± 2.7 μm) and MMZ-IDS (63.5 ± 1.9 μm). The largest marginal gaps were observed in PLD-IDS (81.5 ± 6.3 μm). Two-way ANOVA revealed that the bonding technique (P < .001) and ceramic material (P < .001) both showed significant differences.Conclusions: MMZ produced better marginal accuracy than PLD. IDS seems to have a predisposition to significantly wider marginal gaps than DDS, but these gaps are within the clinically acceptable range. The marginal accuracy of ceramic veneers appears to be related to the bonding technique as well as the material of construction. [ABSTRACT FROM AUTHOR]

Purpose: To investigate the effect of adhesive type and long-term aging on the shear bond strength (SBS) between silicabased ceramics and composite cement (CC). Materials and Methods: Lithium-silicate (LS), feldspathic (FD) and polymer-infiltrated ceramic (PIC) blocks were sectioned (10 x 12 x 2 mm) and divided into 24 groups considering the factors: "ceramics" (LS, FD, and PIC), "adhesive" (Ctrl: without adhesive; 2SC: 2-step conventional; 3SC: 3-step conventional; 1SU: 1-step universal), and "aging" (non-aged or aged [A]). After the surface treatments, CC cylinders (n = 15, ɸ=2mm; height = 2mm) were made and half of the samples were subjected to thermocycling (10,000) and stored in water at 37°C for 18months. The samples were submitted to SBS testing (100 kgf, 1mm/min) and failure analysis. Extra samples were prepared for microscopic analysis of the adhesive interface. SBS (MPa) data was analyzed by 3-way ANOVA and Tukey's test (5%). Weibull analysis was performed on the SBS data. Results: All factors and interactions were significant for SBS (p<0.05). Before aging, there was no significant difference between the tested groups and the respective control groups. After aging, the LS_1SU (22.18±7.74) and LS_2SC (17.32±5.86) groups exhibited significantly lower SBS than did the LS_Ctrl (30.30±6.11). Only the LS_1SU group showed a significant decrease in SBS after aging vs without aging. The LS_1SU (12.20) group showed the highest Weibull modulus, which was significantly higher than LS_2SC_A (2.82) and LS_1SU_A (3.15) groups. Conclusion: No type of adhesive applied after silane benefitted the long-term adhesion of silica-based ceramics to CC in comparison to the groups without adhesive. [ABSTRACT FROM AUTHOR]

Purpose: To compare the fracture resistance of five different groups of chairside CAD/CAM molar crowns fabricated from various lithium disilicate ceramic materials (LDC): one conventional precrystallized CAD/CAM LDC, two novel precrystallized LDCs, and one fully crystallized LDC tested both with and without optional sintering. Materials and Methods: A total of 60 chairside CAD/CAM lithium disilicate molar crowns (n = 12 per group) with 1.5-mm occlusal thickness and a 1.0-mm chamfer finish were designed and fabricated with a chairside CAD/CAM system (CEREC, Dentsply Sirona). The restorations were divided into five groups: (1) IPS e.max CAD; (2) Amber Mill; (3) Straumann n!ce; (4) Straumann n!ce with optional sintering; and (5) Supreme CAD. Restorations were cemented using conventional resin luting cement and primer system to 3D-printed resin dies. Bonded restorations were loaded for 100,000 cycles with 275-N force, and the load at break (LB) and peak load (PL) until fracture were measured. SEM images of fracture surfaces on the printed dies were obtained. Results: Fracture resistance was significantly different depending on the material. Supreme CAD showed the highest fracture resistance (LB: 1,557.2 N; PL: 1,785.8 N), followed by Amber Mill (LB: 1,393.0 N; PL: 1,604.2 N) and IPS e.max CAD (LB: 1,315.7 N; PL: 1,461.9 N). Straumann n!ce without (LB: 862.4 N; PL: 942.9 N) and with the optional sintering (LB: 490.4 N; PL: 541.0 N) showed significantly lower fracture resistance than the others. Conclusion: The fracture resistance of chairside CAD/CAM lithium disilicate molar crowns varied depending on the material, and the novel materials did not perform as well as the conventional equivalents. Fully crystallized lithium disilicate ceramic block materials showed lower fracture resistance than precrystallized counterparts and should be used with caution in the clinic, especially with optional sintering. [ABSTRACT FROM AUTHOR]

Purpose: To evaluate the fracture-behavior of monolithic crowns made of lithium disilicate (IPS e.max CAD, Ivoclar Vivadent; IniBal LiSi Block, GC Dental) and zirconia-reinforced lithium silicate (Celtra Duo, DeguDent; VITA Zahnfabrik) materials before and aKer cyclic faBgue aging. Materials and Methods: Four groups (n = 22/group) of CAD/CAM fabricated upper incisor crowns were produced. All crowns were luted on metal dies with an adhesive dualcure resin cement (G-CEM LinkForce, GC Dental). Half of the crowns in each group (n = 11) were staBcally loaded unBl fracture, without aging. The remaining crowns were subjected to cyclic faBgue aging for 120,000 cycles (Fmax = 220 N) and then loaded staBcally unBl fracture. The fractured models were then visually examined. Scanning electron microsopy (SEM) and energy-dispersive spectroscopy (EDS) were used to evaluate the microstructure of CAD/CAM ceramic materials. The data were staBsBcally analyzed with two-way ANOVA followed by the Tukey HSD test (a = .05). Results: Before cyclic aging, there was no staBsBcally significant difference in load-bearing capacity among the four groups (P = .371). AKer cyclic aging, load-bearing capacity significantly decreased for all groups (P = .000). While the e.max CAD blocks had significantly higher load-bearing capacity (1061 ± 94 N) than both monolithic ceramic crowns (load-bearing capaciBes of the groups) (P < .05), no significant difference was obtained with the IniBal LiSi Block group (920 ± 140 N) (P = .061). Conclusions: The mechanical performance of monolithic ceramic crowns fabricated from lithium disilicate was befer than zirconia-reinforced lithium silicate aKer cyclic faBgue aging. [ABSTRACT FROM AUTHOR]

Many ceramic materials transform to a solid-solution intermediate state before amorphization under extreme conditions. Combining in-situ irradiation experiments and ab initio molecular dynamics simulations, we performed a comparative study of the defect accumulation process in MAX phases, Ti 2 AlC, Cr 2 AlC, and Ti 2 SnC, to clarify the correlation between solid-solution intermediate phase properties and phase instability. It is found that phase stability strongly depends on the lattice distortion of the solid-solution intermediate state, rather than the defect energies in the initial phases that were previously believed as the indicator of the resistance to the irradiation-induced amorphization. Larger lattice distortions of the solid-solution intermediate state can hinder defect recombination and lead to faster collapse to an amorphous state. This work provides a new research insight into phase instability for ceramic materials under extreme conditions. [ABSTRACT FROM AUTHOR]

Applications of praseodymium doped ceria (PDC) in solid oxide fuel cells require a deep insight into the thermal expansion, stresses, and ionic conduction. Nonetheless, the investigation of thermo-mechanical properties and oxygen vacancy diffusion remains incomplete. Based on free Helmholtz energy, we formulate analytical expressions to directly connect thermal expansion coefficient, elastic moduli, oxygen vacancy–dopant binding and oxygen vacancy migration energies by employing statistical moment method (SMM). The SMM calculations capture the full anharmonicity of lattice thermal vibrations. Our analyses report the significant influences of temperature and dopant content on the thermal expansion coefficient, bulk and Young's moduli, oxygen vacancy–dopant binding and oxygen vacancy migration energies, and ionic conductivity. The role of Pr dopant on the oxygen vacancy diffusion is fully described by combining the symmetric energy profiles related to blocking effect and asymmetric energy profiles generated from trapping effect. By switching van der Waals (vdW) forces on and off in the SMM calculations, we first show that the vdW forces cause a positive effect on the mechanical properties but reduce the thermal expansion and resist the oxygen vacancy diffusion. Our findings are discussed concerning the results from other calculations and experiments in the literature. The insights on the thermo-mechanical properties and oxygen vacancy diffusion for PDC crystal can be generalized and applied to other ceramic materials that are essential for solid state batteries. [ABSTRACT FROM AUTHOR]

Monazite, with its unique chemical composition and stable crystal structure, shows significant potential for immobilizing high-level radioactive waste. In this study, a series of monazite ceramics were synthesized to study the effect of entropy change on their structure and aqueous durability. The synthesized ceramics exhibit a monoclinic structure (P2 1 /n), with an average grain size below 80 nm. MCC-1 leaching tests reveal that the normalized leaching rate decreases over time but increases with higher entropy. The five-element high-entropy ceramics have an average leaching rate of 4.2 × 10⁻³ g·m⁻2 d⁻1. Notably, the higher leaching rate in high-entropy nanocrystalline monazites is likely attributed to the reduced grain size. The presence of numerous grain boundaries tends to mitigate the precipitation inhibition effect typically associated with high-entropy ceramics. These findings offer insights into the role of entropy and grain size in ceramic materials for radioactive waste immobilization. [ABSTRACT FROM AUTHOR]

In this study, ZrB 2 -SiC-ZrC (ZSZ) composite powders with molar ratios C/(B + Zr + Si) = 1.5, 1.9 and 2.4 were obtained by sol-gel method and boro/carbothermal reduction reaction. Meanwhile, the impact of heat treatment temperature (1100 °C–1600 °C) and holding time (1 h–2.5 h) on the resulting powders were studied. The results showed that the ZSZ powder precursors were first completely converted to ZrO 2 , SiO 2 , B 2 O 3 and pyrolytic carbon after heat treatment at 1200 °C under the optimized molar ratio (2.4) and holding time (2.5 h). Then, the transformed oxidation products and pyrolytic carbon were completely transformed into ZSZ composite powders after optimized heat treatment at 1500 °C. The synthesized ZSZ composite powders are characterized by the core-shell structure, in which ZSZ particles act as the inner core are encapsulated by the low-crystalline ZrB 2 phase as the outer shell to form a core shell structure. The ZSZ composite ceramic materials prepared using the core-shell structural powders have excellent ablative properties in the range of 2000 °C, with the mass and line ablation rate of −3.5 × 10−4 g/cm3 and 2.39 × 10−3 mm/s, respectively. [ABSTRACT FROM AUTHOR]

Low thermal conductivities and high thermal expansion coefficients are desirable for rare-earth zirconate thermal barrier coating materials. Introduction of cation doping and adjustment of the nonstoichiometry are efficient methods for enhancing the thermophysical characteristics of materials. Herein, the thermophysical properties of Yb3+-doped nonstoichiometric gadolinium zirconate ceramic materials were investigated using first-principles calculations and solid-state reaction techniques. As the Yb3+ content increases, additional cations enter the interstitial spaces (for excess Gd3+ gadolinium zirconate) and form vacancy defects (for excess Zr4+ gadolinium zirconate), which serve as phonon scattering centres to decrease the thermal conductivity. When Yb3+ is doped at the same concentration, gadolinium zirconate with excess Zr4+ exhibits a lower thermal conductivity. Specifically, Gd 1.875 Yb 0.25 Zr 2.125 O 7 shows the lowest minimum thermal conductivity of 1.133 W/(m⸱K) (according to the Clark model) and 1.241 W/(m⸱K) (according to the Cahill model). In addition, the experimental results also suggest that the optimal content of Yb3+ is 0.25 excess Zr4+ gadolinium zirconate, which has the lowest intrinsic thermal conductivity of 1.037 W/(m⸱K) at 1300 K. Moreover, the thermal expansion coefficient of the Yb3+-doped excess Gd3+ nonstoichiometric material is greater than that of the doped excess Zr4+ material, this is due to the greater electronegativity difference between Yb3+ and Zr4+ than that between Yb3+ and Gd3+ and the lower binding energy of Gd-O than that of Zr-O. The experimental results and the calculated results are in good agreement. The aim of this work is to enhance the thermophysical characteristics of gadolinium zirconate ceramics for use as thermal barrier coating materials. [ABSTRACT FROM AUTHOR]

Gadolinium gallium aluminum garnet doped with cerium (GGAG:Ce), a promising ceramic scintillator material, is being excessively explored for its high quality optical properties by the bandgap engineering with different Ga/Al ratio. In this study, GGAG:Ce powders were synthesized using a solvothermal method and sintered at 1300 °C to investigate the impact of the gallium-to-aluminum (Ga/Al) ratio on optical characteristics. The results revealed that a decrease in the Ga/Al ratio led to a decrease in particle size. This observation can be attributed to the different reactivity and growth kinetics of gallium and aluminum precursors during the solvothermal process. Perturbations from the optimized Ga/Al ratio of 1.5–1.77 and 1.27 resulted in substantially enhanced photoluminescence (PL) and radioluminescence (RL) spectra intensities. PL lifetime measurements of various Ga/Al ratio exhibit average PL lifetime between 48 and 57 ns. Specifically, the deviations to 1.77 and 1.27 ratios yielded approximately 125 % and 106 %, respectively, in observed luminescent measurements compared to other ratios. This enhancement in PL and RL intensity suggests that the Ga/Al ratio plays a critical role in modulating the optical properties of GGAG:Ce ceramic powders. The results of this study also highlight the importance of the Ga/Al ratio in tailoring the optical or luminescence characteristics of GGAG:Ce powders. [ABSTRACT FROM AUTHOR]

A CO 2 -stable, easily sintered proton-conducting oxide electrolytes based on solid solution Ba 7 In 6 Al 2– x Zn x O 19-0.5 x with hexagonal structure has been synthesized for the first time. Within the homogeneity region (0 ≤ x ≤ 0.10), there is an increase in unit cell parameters, cell volumes and free cell volumes. The addition of Zn2+ markedly improved the sinterability of the material. The relative density of the ceramics of the doped samples reached 95 % at lower sintering temperatures than the parent phase. The electrical conductivity was studied using electrochemical impedance spectroscopy. Upon doping the oxygen-ion conductivity increased by 0.25 orders of magnitude at 800 °C. Proton transport was predominant below 500 °C for a wet atmosphere (pH 2 O = 1.92·10−2 atm). The investigated phases Ba 7 In 6 Al 2– x Zn x O 19-0.5 x are capable of hydration and incorporate up to 1.45 mol H 2 O vs 0.41 mol H 2 O for the parent phase. The studied phases exhibit chemical resistance to CO 2 under heat treatment at 600 °C. It was shown that solid solution Ba 7 In 6 Al 2– x Zn x O 19-0.5 x is a promising electrolyte material for intermediate-temperature fuel cells. [Display omitted] • The Zn-doping in solid solution Ba 7 In 6 Al 2– x Zn x O 19-0.5 x markedly improved the sinterability of the material and well-sintered ceramics were obtained with relative density 95 %. • The water uptake increased with increasing Zn-concentration. • Ba 7 In 6 Al 2– x Zn x O 19-0.5 x phases were protonic conductors at T < 500 °C in wet air. • Ba 7 In 6 Al 2– x Zn x O 19-0.5 x phases exhibited chemical resistance to pure CO 2. [ABSTRACT FROM AUTHOR]

Ti doping can improve the interfacial wettability and bonding condition between ZTA ceramic and high chromium cast iron (HCCI), but the underlying mechanism is still unclear. Therefore, the effects of Ti doping on the interfacial characters between ZTA and HCCI were investigated by experiment and first-principles calculations. Results of XRD, SEM, and high-temperature drop test indicate the presence of Ti at the interface and its effect on the formation of interfacial diffusion layer to improve the interface wettability and bonding obviously. The heat of segregation and work of adhesion obtained by first-principle calculations shows that the improvement in interface wettability and bonding is due to the promotion of dopped Ti atoms on the diffusion of Fe, Al, and Zr elements, but not the diffusion of Ti itself. Further investigation from the electronic level reveals that the doped Ti changes the charge distribution and orbital hybridization, and thus makes the formation or enhancement of strong ionic bonds and covalent bonds at the interface, improving the bonding strength and wettability of interfaces in ZTA/HCCI. The findings of this research can offer new insights into the modification of ceramics and enlarge the application of advanced ceramic materials. [ABSTRACT FROM AUTHOR]

In order to solve the increasingly serious electromagnetic wave pollution, the preparation of high-performance electromagnetic wave absorbing (EWA) materials has been very urgent. High-entropy ceramics have a good prospect in the field of EWA materials due to the unique effect brought by its multi-component elements. Therefore, in this study, the composition of high-entropy ceramics was designed by utilizing the Goldschmid tolerance factor. Then the high-entropy perovskite Ba(Zn 0.2 Yb 0.2 Ta 0.2 Nb 0.2 V 0.2)O 3 ceramic (BZO) with high EWA performance was prepared by high-temperature solid-phase method. The EWA mechanism of the material was explored based on the phase composition, microstructure and electromagnetic parameters of the samples. Good impedance matching and better attenuation ability were obtained for BZO-1100 due to the crystallographic transition and interface increase. As a result, BZO-1100 achieves excellent EWA performance at a thickness of 2.12 mm, with a minimum reflection loss (RL min) of −54.09 dB and an effective absorption bandwidth (EAB) of 2.81 GHz in the X-band. In addition, the possibility of the practical application of the BZO high-entropy ceramics is verified by electric field distribution simulations and RCS simulations. This study provides a valuable reference for the design of high-performance high-entropy perovskite ceramic absorber materials. [Display omitted] [ABSTRACT FROM AUTHOR]

High-entropy ceramic materials are promising for creating functional ceramics for various purposes. The unique properties of such materials make it possible to create new thermal barrier coatings based on them. Reducing costs, time and simplifying the technology of synthesis of high-entropy ceramics is the subject of numerous studies. In this work, the synthesis of high-entropy ceramics (Y 0,2 Yb 0,2 Lu 0,2 Eu 0,2 Er 0,2) 3 Al 5 O 12 in a powerful beam of fast electrons was carried out for the first time. A powder mixture of initial oxides, placed in the volume of a massive copper cell, was exposed in air to a short-term exposure to a beam of powerful fast electrons with an energy of 2 MeV and a beam current of 12 mA. The speed of movement of the cuvette with the powder mixture under the beam was 1 cm/s. The total irradiation time was 10 s. During the irradiation process, at least 96 % of the mass of the powder mixture melted, resulting in the formation of highly porous ceramic formations in the form of droplets. X-ray phase analysis showed that the melt droplets are high-entropy ceramics (Y 0,2 Yb 0,2 Lu 0,2 Eu 0,2 Er 0,2) 3 Al 5 O 12. The powder product remaining in the cuvette and not participating in the formation of droplets contains phases of the original oxides and intermediate phases of synthesized high-entropy ceramics. Electron microscopy with EDS showed a uniform distribution of elements on the surface and in the volume of the formed ceramic droplets. [ABSTRACT FROM AUTHOR]

Donor-doped SrNb 2 O 6 -based materials are regarded as highly promising candidates for high-temperature thermoelectric applications. The Sr 0.6 La 0.4 Nb 2 O 6-δ /x wt% Ti (x = 1, 5, 10, 15) composite ceramics thermoelectric materials were prepared and the mechanism for enhancing their thermoelectric properties was investigated. The experimental results demonstrate that during sintering, nano-additive titanium powder undergoes oxidation to form TiO 2. The inclusion of a secondary phase ultimately leads to successful reduction in electrical resistivity within the composite oxides. Due to crystal defects, complex structure and phonon scattering at grain boundaries, the samples consistently exhibit low thermal conductivity values below 3.0 W m−1K−1. Among them, the sample doped with 10 wt% Ti shows the highest PF value (470.0 μW/mK2 at 1073 K), demonstrating a significant increase in power factor of 280 % compared to Sr 0.6 La 0.4 Nb 2 O 6 without the Ti composite. Consequently, the Sr 0.6 La 0.4 Nb 2 O 6-δ /10 wt% Ti composite material achieved a maximum ZT value of 0.20, representing a fifty-three percent enhancement compared to the undoped sample. [ABSTRACT FROM AUTHOR]

Rare earth ions doped ferroelectric ceramics have attracted much attention because rare earth ions can effectively regulate the ferroelectric and energy storage properties of ceramics. Herein, Ba 1- x Ca x Ti 1- y Hf y O 3 ceramics modified with Ca2+ and Hf4+ are prepared, and the effects of different Ca2+ and Hf4+ concentrations on the crystal structure, microstructure and electrical properties of Ba 1- x Ca x Ti 1- y Hf y O 3 ceramics are investigated. Through the analysis on the ceramic structure and electrical properties, Ba 0.96 Ca 0.04 Ti 0.85 Hf 0.15 O 3 (BCTH) ceramic shows excellent comprehensive performance. Using BCTH ceramic as matrix material, the influences of different Pr3+ concentrations on the structure and electrical properties of the BCTH: x %Pr3+ ceramics are studied. Energy storage efficiency (η) gradually increases with the increase of Pr3+ concentration, while the energy storage density (W d) shows a trend of first increasing and then decreasing, reaching the maximum value for x = 0.6 (W d = 0.338 J/cm3, η = 87.86 %), which was higher than that of pure BCTH ceramics (W d = 0.212 J/cm3, η = 78.05 %) increased by 59.43 % and 12.57 %, respectively. All the samples show good stability of energy storage temperature and frequency. After Pr3+ doping, the Curie transition temperature of the ceramics first increas and then decreases, and show a wider transition peak, indicating that the transition from ferroelectrics to relaxation ferroelectrics occurres. The excellent electrical properties of BCTH: x %Pr3+ ceramics indicate their potential application value in the field of electricity. [ABSTRACT FROM AUTHOR]

Mesoporous ceramic materials used in applications such as catalysis, filtration, or sensing, are usually hierarchically structured. Thereby, their structural hierarchy is often inherently related to the manufacturing methods and cannot be independently locally designed along all length scales. This study combines light‐based additive manufacturing and bottom‐up light‐induced self‐assembly (LISA) sol‐gel chemistry to engineer hierarchically structured porous silica from the nanoscale to the macroscopic object geometry. A LISA‐based printing solution that enables printing of ordered mesoporous silica with geometrically complex shapes by using a commercially available digital light processing (DLP)‐based 3D printer is presented. This approach exploits the self‐assembly process of block copolymer mesopore templates, such as Pluronic P123, and hydrolysis and condensation of silica precursors upon irradiation in the 3D printer to shape mesoporous silica objects. Furthermore, different resins are added to the LISA solution to print 3D silica‐resin objects. Mesoporous silica objects up to 10 mm in size, consisting of ordered mesopores with diameters around 5 nm and having high specific surface areas of ≈400 m2 g−1 are successfully printed with a fast and easy post‐processing. [ABSTRACT FROM AUTHOR]

Coal gangues i a solid waste during the coal mining process and the accumulation of coal gangue will harm the environment. Therefore, solid waste utilization of coal gangue is required to reduce the environmental damage. In this paper, cordierite ceramics are successfully prepared via a solid‐phase sintering using coal gangue, Al2O3, and MgO as raw materials. The effects of sintering temperatures on the microstructures, phase stability, and thermal properties of ceramics are investigated. The results show that the properties of cordierites prepared at 1200°C are close to those of prepared by the traditional method, and the synthesized ceramics have thermal expansion coefficients (TECs) and conductivity of 4.1–10−6 K−1 and 1.72 W·m−1 K−1 at 900°C, respectively. The sample prepared at 1200°C has good wear resistance (η) with a wear resistance coefficient of 0.507, and an excellent thermal shock resistance, which can withstand 15 times of cold and hot shocks at 1100°C without any cracks on the surface. This study systematically elucidates the thermal/mechanical properties of the synthesized cordierite, and the feasibility of using coal gangue as raw materials prepared cordierite ceramics as refractory materials. This work presents an effective solution to mitigate the challenge of coal gangue disposal. [ABSTRACT FROM AUTHOR]

This review paper explores the use of red mud as a sustainable alternative for construction materials and soil stabilisation due to its unique chemical and mineral composition, a waste produced during the extraction of aluminium from bauxite ore. The disposal of red mud is a major environmental issue worldwide due to its high alkalinity and large production volume. Although this material has already been utilised as construction material (e.g., bricks, cement, concrete), it can also be incorporated for waste water treatment and lead to waste reduction. In soil stabilisation, red mud's alkaline nature, pozzolanic properties, and fine particle size improve soil structure and strength, offering a cost-effective solution. Utilising red mud as a filling material for low-lying areas addresses the disposal problem while contributing to infrastructure development projects. This study highlights construction materials' mechanical properties and durability by incorporating bauxite tailings and also incorporating valorisation of red mud as a precursor for alkali-activated binder. This paper comprises recent research findings and practical applications associated with the use of this waste. Also, it discusses the benefits and challenges associated with the large-scale use of red mud. It gives an idea about how the strength and durability of construction materials can be improved considering overall environmental impact. Future perspectives on policy, technology, and environmental impact are also discussed to provide a comprehensive understanding of red mud's potential for sustainable development. Article Highlights: Red mud enhances the properties of materials like strength, durability, and thermal resistance of construction materials like bricks, ceramic, and cement. Red mud increases soil load-bearing capacity, reduces plasticity, and enhances erosion resistance, making it ideal for foundations and road construction. Using red mud reduces dependency on traditional raw materials, conserving natural resources and lowering environmental impacts. Red mud in construction and soil stabilisation contributes to durable, eco-friendly structures and supports sustainable land use. [ABSTRACT FROM AUTHOR]

ABSTRACT Objectives Material and Methods Results Conclusions Clinical Significance To analyze survival and complication rates for anterior and premolar laminate‐veneers out of different ceramic materials (feldspathic, leucite‐reinforced glass–ceramic [LRGC], lithium‐disilicate [LDS] and zirconia).A systematic literature search was conducted across multiple databases for clinical studies on ceramic laminate‐veneers with a minimum‐follow‐up of ≥ 1 year. The date of last search was on February 19, 2024. Survival, technical, esthetic and biological events were assessed for different laminate‐veneer materials at three observation periods (short‐ [1–3 years], mid‐ [4–6 years] and long‐term [≥ 7 years]).Twenty‐nine studies were included. Meta‐analysis revealed a pooled survival‐rate of 96.13% for feldspathic, 93.70% for LRGC and 96.81% for LDS at 10.4 years. No difference was found between materials. Complication rates (technical/esthetic/biological) were as follows: Feldspathic: 41.48%/19.64%/6.51%; LRGC: 29.87%/17.89%/4.4%; LDS: 6.1%/1.9%/0.45% at 10.4 years. Zirconia showed a 100% survival‐rate with no complications at 2.6 years. No long‐term data was available for zirconia.Feldspathic, LRGC and LDS laminate‐veneers showed high survival‐rates at long‐term observation. LDS slightly outperforms feldspathic and LRGC laminate‐veneers with lower long‐term complication rates. More studies providing long‐term data on zirconia laminate‐veneers are needed.Ceramic laminate‐veneers are a reliable treatment option. LDS may be preferred as a restorative material for long‐term success. [ABSTRACT FROM AUTHOR]

A major challenge in the application of ceramic materials is a trade‐off between strength and toughness. In this work, hierarchically structured ceramic coatings (HSCCs) are fabricated to address this challenge. HSCCs feature a dual‐layer micron‐scale structure built on a “brick‐mortar” nanoscale structure, which is achieved by changing the crystalline and amorphous phase ratio during plasma electrolytic oxidation (PEO). It is found that HSCCs with homogeneous interfaces exhibit high thermal stability up to 700 °C and a 65% improvement in shear strain resistance compared to conventional crystalline coatings (CCCs). This improvement is attributed to the stabilizing effect of atoms on the boundaries of the enhancement phase and the facilitating effect on the deformation of the compliant phase. The hierarchical structure effectively leverages the plasticity of the compliant phase and the strength of the enhancement phase facilitated by the homogeneous interface. This work proposes a feasible approach for improving the toughness of ceramic functional composites and mitigating their susceptibility to brittle fracture. [ABSTRACT FROM AUTHOR]

All‐solid‐state batteries relying on Li metal as negative electrode material and a ceramic electrolyte may severely suffer from unwanted interfacial processes. Here, Li1.3Al0.3Ti1.7(PO4)3 (LATP) serve as a model electrolyte which is known to form an ionic‐electronic, that is, mixed conducting interphase (MCI) when in contact with metallic Li or any other Li source. Li1.3+xAl0.3Ti1.7(PO4)3 with x = 0.2, 0.6 and 1.3 is prepared via ex situ chemical lithiation to mimic the formation of MCIs taking place otherwise operando. The preparation of large amounts of lithiated LATP with controlled Li contents allowed us to use nuclear and electric techniques to study local structures and ionic/electronic dynamics in detail. The results point to the formation of a core‐shell two‐phase morphology with the Li‐rich Li3Al0.3Ti1.7(PO4)3 phase covering the nonlithiated Li‐poor regions. The originally poor electronic conductivity σeon of 6.5 × 10−12 S cm−1 (293 K) increases by ≈3 orders of magnitude, hence reaching the order of 6.6 × 10−9 S cm−1 for x = 0.6. At even higher loadings (x = 1.3), a decrease in conductivity is seen, i.e., not exceeding alarming values for σeon. Quantifying electronic and ionic transport processes will help assessing the extent of damage through MCI formation and discussing whether any strategies to mitigate such formation is necessary at all. [ABSTRACT FROM AUTHOR]

With the development of the electronic packaging industry, there is an increased demand for enhanced strength in DBA substrates. Ultrasonic soldering technology allows low-temperature joining of ceramic-metal materials under ambient air conditions. In this paper, we successfully achieved the joining between AlN ceramics and 2024Al using Sn9Zn solder and ultrasonic soldering technique, while also analyzing the joining mechanism through Comsol software simulations. It was observed that under the appropriate ultrasonic amplitude and frequency, the Sn9Zn solder exhibited complete wetting with both base materials, resulting in reliable joints. Building upon this finding, the conventional Sn9Zn solder was further optimized by adding Sb element. The addition of Sb element led to the formation of Zn 4 Sb 3 phase and β-Sn(Sb) phase with Sb acting as solute. Among them, the generation of β-Sn(Sb) solid solution phase effectively improved the joint strength. The maximum joint strength was achieved at an average value of 75.066 MPa when the Sb content reached 1 wt. %. At this point, the failure occurred within the AlN ceramic base material. [ABSTRACT FROM AUTHOR]

SiC whiskers (SiC w)-reinforced α/β-SiAlON ceramic tool materials were synthesized via spark plasma sintering (SPS). A comprehensive study was conducted on densification mechanism, phase composition, microstructure, mechanical properties, and wear resistance of the SiC w /α/β-SiAlON composites. The results indicated that SiC w constrained the densification process and impeded the growth of SiAlON grains, and the introduction of SiC w significantly enhanced mechanical properties of the α/β-SiAlON ceramic. The composite containing 28 wt% SiC w synthesized at 1700 °C showed well mechanical properties, with a density of 3.35 g/cm³, Vickers hardness of 19.38 ± 0.33 GPa, and fracture toughness of 7.35 ± 0.27 MPa m1/2.The principal toughening mechanisms of SiC w /α/β-SiAlON included crack deflection, branching, bridging, as well as transgranular fracture and whisker pullout. The addition of SiC w improved the wear resistance of α/β-SiAlON ceramic. Compared to those without whiskers, the wear volume and wear rate were decreased by 38.8 %. [ABSTRACT FROM AUTHOR]

Fluorapatite glass-ceramic (GC) and yttria-stabilized zirconia (YSZ) are two commonly used ceramic materials for dental prosthetic restorations. Fluorapatite GCs are known for their outstanding biocompatibility and aesthetic characteristics, moreover, they can release fluoride ions which have anticaries effect. Nevertheless, they often lack the requisite strength and toughness to withstand high occlusal forces. Conversely, YSZ exhibits remarkable mechanical properties, however, it is susceptible to excessive wear on opposing teeth. To address these limitations, a novel fluorapatite GC-YSZ composite ceramic was designed and formed through vat photopolymerization. The effect of composition ratios of fluorapatite GC particles and YSZ fibers (0˗40 wt% YSZ) on the forming precision, mechanical properties, and tribological compatibility with GC was thoroughly investigated. The results demonstrated that optimal comprehensive performance was achieved when the YSZ fiber content reached 40 wt%, which resulted in a fracture toughness of 1.68 MPa m1/2, marking a 98.8 % increase over pure GC. The specific wear rates of the sample and the antagonistic titanium ball were reduced by 75.6 % and 63.8 %, respectively, compared with GC. In addition, the dimensional accuracy error of the green body was reduced by approximately 44 %. The design and fabrication of GC-YSZ composites offer an approach for developing high-performance all-ceramic dental materials. [ABSTRACT FROM AUTHOR]

Highly robust ceramics materials are promising materials for applications in the automobile, aerospace, and ceramic cutting tool industries. However, conventional ceramics are typically brittle, which limits their suitability for advanced applications. In this study, with zeolite imidazolium salt skeleton-8 (ZIF-8) as a carbon source, discharge plasma sintering is used to create carbon nanonetworks derived from metal-organic frameworks (MOFs) in situ on the grain boundaries of zirconia-toughened alumina (ZTA) ceramic. ZTA exhibits maximum bending strength (719 ± 20.5 MPa) and fracture toughness (7.91 ± 0.7 MPa m1/2) at MOF concentrations of 1.0 wt% and 2.0 wt%, respectively, which are 1.37 and 1.88 times higher than that of the unmodified sample. This demonstrates that the MOF-derived carbon nanonetworks significantly improve the mechanical properties of the ceramic. The finite element analysis results indicate that the carbon nanonetworks can effectively disperse the stress inside the material and transfer the concentrated stress from the internal defects to the two-phase grain boundary on the surface of the sample, thereby contributing to strengthening and toughening. Overall, this work validates that the in situ production of carbon nanonetworks from MOFs is an effective strategy to enhance the mechanical properties of ZTA ceramics. Moreover, it offers new approaches for reinforcing and toughening other ceramic materials. [ABSTRACT FROM AUTHOR]

Develop a sustainable bovine hydroxyapatite dental ceramic with the addition of titanium dioxide (TiO 2) nanoparticles (5 % and 8 % by weight), analyzing the outcome of this addition to the microstructure, as well as its mechanical and chemical properties, in order to evaluate whether they satisfy the International Organization for Standardization (ISO) 6872:2015 for dental ceramics or not. Disks were obtained through uniaxial followed by isostatic pressing from bovine hydroxyapatite powder and TiO 2 nanoparticles and sintered at 1300ºC for 2 h. Three experimental groups were developed (HA, HA+5 %TiO 2 and HA+8 %TiO 2) and subjected to X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), indentation fracture (IF), biaxial flexural strength (BFS) and chemical solubility test. XRD revealed, for HA group, the appearance of a peak corresponding to b-tricalcium phosphate (ß-TCP). For HA+ 5 %TiO 2 and HA+ 8 %TiO 2, the entire composition was converted into ß-TCP and calcium titanate (CaTiO 3). The SEM images showed a dense ceramic matrix and a uniform distribution of another phase in groups with TiO 2 nanoparticles. HA+ 5 %TiO 2 (1.40 ± 0.18 MPa.m1/2) and HA+ 8 %TiO 2 (1.32 ± 0.18 MPa.m1/2) showed significantly higher fracture toughness values than HA (0.67 ± 0.09 MPa.m1/2). HA showed significantly higher characteristic stress (295.8 MPa) in comparison to groups with 5 % (235.1 MPa) and 8 % (214.4 MPa) TiO 2 nanoparticles. Differences were not observed between the Weibull modulus values. The solubility results indicated that all experimental ceramics were above the 2000 ug/cm2 limit set by the ISO 6872:2015. This study proposed the development and characterization of a new ceramic for dental prosthesis made from HA extracted from bovine bones, with the intention of reusing these solids waste and transforming them into a sustainable and low-cost material. Although the experimental calcium phosphate ceramic with additions of 5 % and 8 % of TiO 2 achieved desirable mechanical properties, the chemical solubility values were very high. [Display omitted] • Bovine HA derived bioceramic with TiO 2 presents sustainability potential. • The addition of 5 % and 8 %TiO 2 significantly improved material's fracture toughness. • HA + TiO 2 bioceramic material converted microstructure to ß-TCP and CaTiO 3. • HA+TiO 2 achieved mechanical ISO standards, but failed chemical solubility limits. [ABSTRACT FROM AUTHOR]

Lead halide perovskite quantum dots (PeQDs) have garnered increasing attention due to their extraordinary optoelectronic properties. In recent years, femtosecond (fs) laser direct writing shows to be an effective way of inducing localized crystallization of PeQDs inside glass matrix while remaining their structural stability and optical performance. This article reviews the research progress on fs laser irradiation‐induced nucleation/growth of PeQDs in glass and discusses the latest advancements in the use of the technology for optical data storage, micrometer‐scale light‐emitting diode (LED), information security protection, and other related fields. It offers novel insights and perspectives for exploring new functionality and device application of fs laser‐printed PeQDs glass composite structures. [ABSTRACT FROM AUTHOR]

Background: Surface treatment of the intaglio surface of zirconia is important for bonding. However, it could affect the strength of the materials. The purpose of this study is to compare the effect of laser, etching, and air abrasion surface treatment methods to a control group on the flexural strength of three zirconia materials with two different thicknesses. (1) Methods: A total of 120 disks were divided into three groups according to the type of zirconia and the ceramic thickness. Then, according to the surface treatment method, the groups were divided into four subdivisions. The change in the microstructure of the ceramic material was investigated through Scanning Electron Microscope (EVO LS10, Carl Zeiss SMT Ltd. Oberkochen, Germany). Phase identification was performed using an X-ray diffraction device (XRD; Ultimate IV X-ray Diffractometer, Rigaku Inc., Tokyo, Japan). The flexural strength was assessed with a biaxial flexural strength test in a universal testing machine. Data were analyzed using SPSS Software (SPSS version 26.0.Armonk, NY: IBM Corp). A three-way ANOVA and a post hoc Dunnett T3 test were employed to evaluate the effect of the yttria concentration, thickness, and surface treatment on the flexural strength of zirconia (α = 0.05). (2) Results: At 0.8 mm thickness, air abrasion significantly increased the flexural strength of 3Y-TZP (1130.6 ± 171.3 MPa) and 4Y-TZP (872 ± 108.6 MPa). However, air abrasion significantly decreased the flexural strength of 5Y-TZP materials (373 ± 46.8 MPa). Laser irradiation significantly decreased the flexural strength of 5Y-TZP (347 ± 50.3 MPa), while etching significantly decreased the flexural strength of both 3Y-TZP (530 ± 48.8) and 4Y-TZP (457.1 ± 57.3). When the thickness increased to 1 mm, air abrasion continued to significantly decrease the flexural strength of 5Y-TZP materials. (3) Conclusions: There was a negative effect of surface treatment on the flexural strength at 0.8 mm thickness rather than at 1 mm thickness. Air abrasion enhances the flexural strength of 3Y-TZP and 4Y-TZP materials but significantly reduces the flexural strength of 5Y-TZP materials. Zircos-E etching and Er:YAG surface treatment methods did not significantly reduce the flexural strength of 5Y-TZP materials at 1 mm thickness and can be recommended as an alternative surface treatment for 5Y-TZP materials. [ABSTRACT FROM AUTHOR]

A radiochemical procedure has been developed for the quantification of uranium and thorium isotopes in NORM samples from the ceramic industry, such as zirconium sands, zirconium flours, micronized zircon, pigments and personal aerosol filters. The method is based on a fusion pretreatment with borate salts, a separation with anion exchange resins and alpha-particle spectrometry measurement. This method is an alternative to gamma spectrometry when the amount of sample is extremely small (2–10 mg) as in the case of aerosol filters, or there is no secular equilibrium in the 238U and 232Th chains, as in the ceramic pigments. The method has been validated with different ceramic materials and the comparison of the results with gamma measurements. Its reproducibility was also checked with different sample masses. [ABSTRACT FROM AUTHOR]

The social progress, economic growth, and meteoric urbanization prompt the exploitation of available resources triggering the contagion of the biological and physical elements of the atmosphere irrationally causing global environmental pollution. Environmental contamination monitoring is a dire necessity. Although a number of technologies find mention in the literature for environmental remediation, however, environmental catalysis is an advanced steadily growing technique for pollution abatement. In this dimension, ceramic materials have turned heads due to their wide‐scale application areas. Hitherto, research is being done on advanced ceramics to fabricate novel modules for energy storage applications, in designing green buildings, pollution rheostats, and environmental engineering. This article deals with the abatement of environmental contaminants by adopting various methodologies such as aerobic and anaerobic biological treatments, adsorption, chemical oxidation, membrane separation, photocatalysis, ozonation using the ceramic as precursor materials. The ceramic membranes are cost‐effective, ecofriendly, efficacious, and green approach to obliterate toxins and harmful gases released in environment. Even though, limited literature is available on the abolition of harmful contaminants from air and soil using ceramic materials, an attempt has been made to present currently available data with best of our knowledge. This article will sensitize researchers to refabricate novel materials for environment sustainability. [ABSTRACT FROM AUTHOR]

The thermal shock resistance of ceramics is a key factor for determining the durability of ceramic components under transient thermal conditions and is also one of the key factors for evaluating the stability of ceramics under extreme thermal conditions. After rapid heating or cooling, the surface and internal thermal stress mismatches of ceramics can cause severe thermal damage. Two main types of ceramic thermal shock exist: rapid cooling and rapid heating thermal shock. This article presents a broad understanding and insight into fundamental theory and experimental methods for ceramic thermal shock testing. The experimental equipment and procedures, test result evaluation, and material characterization of ceramic thermal shock are summarized. Moreover, outlooks and perspectives are discussed for testing and characterizing ceramic thermal shock resistance. This review will be helpful to researchers performing studies in the relevant fields of ceramics. [ABSTRACT FROM AUTHOR]

Dysprosium (Dy)‐doped (Y1−xDyx)3Si2C2 (x = 0, 0.1, 0.3, 0.5) solid solution ceramics were successfully fabricated using an in situ reaction spark plasma sintering technology, for the first time. The effect of various Dy doping contents (x) on the microstructure, mechanical, and thermal properties of (Y1−xDyx)3Si2C2 ceramics was investigated. The (0 2 0) crystal plane spacing of (Y0.5Dy0.5)3Si2C2 was 7.813 Å, which was smaller than that of Y3Si2C2, due to the fact that the atomic radius of Dy is smaller than that of Y. The Dy doping facilitated the consolidation of (Y1−xDyx)3Si2C2, thus a highly dense (Y0.5Dy0.5)3Si2C2 ceramic material with a low open porosity of 0.14% was successfully obtained at a relatively low temperature of 1 200°C. As the content of Dy doping (x) increased from 0 to 0.5, the purity of (Y1−xDyx)3Si2C2 ceramics increased from 88.3 to 90.7 wt.%, while the grain size of (Y1−xDyx)3Si2C2 ceramics decreased from 0.59 to 0.46 µm. As a result, the Vickers hardness and thermal conductivity of the (Y0.5Dy0.5)3Si2C2 material was 7.1 GPa and 9.8 W·m−1·K−1, respectively. [ABSTRACT FROM AUTHOR]

Knowledge about the thermodynamic equilibria of the Al 2 O 3 –TiO 2 –CaO system is important for the design of refractory and ceramic materials. The Al 2 O 3 –TiO 2 , Al 2 O 3 –CaO and CaO–TiO 2 binary systems were reoptimized and the Al 2 O 3 –TiO 2 –CaO ternary system was assessed by CALPHAD (CAlculation of PHAse Diagram) approach due to the reliability of phase diagram and thermodynamic property data. The liquid phase was described by the ionic two-sublattice model with the formula (Al+3,Ti+2,Ti+3,Ca+2) P (O−2,AlO 1.5 ,Va,O,TiO 2) Q. A set of self-consistent thermodynamic parameters for the Al 2 O 3 –TiO 2 –CaO ternary system was finally obtained, reproducing well the phase diagram and thermodynamic properties, predicting the Ca 4 Ti 3 O 10 primary crystallization field. The present thermodynamic description is of interest for the design of refractory and ceramic materials as well as the development of thermodynamic databases for multicomponent aluminosilicate system. [ABSTRACT FROM AUTHOR]

Synthesis of porous ceramic materials based on fine SiC with sintering silicon oxide and magnesia binders at T = 800–1300 °C is considered. Special attention is paid to the influence of the shape and morphology of the initial powder particles on structural parameters and characteristics of porous ceramic materials. The SiC membranes sintered at 1000–1300 °C had average pore sizes of 0.5–1 μm, open porosity - up to 50 %, bending strength - up to 48.5 MPa and high water permeance - up to 7890 l⋅m−2⋅h−1⋅bar−1. The established filtration efficiency was ∼99 % in the case of screening out model particles of D 50 = 0.5 μm in size with maintaining stable permeance and physico-mechanical characteristics after multiple filtration-regeneration cycles. Comprehension of the initial powders morphology impact on the synthesized porous ceramics parameters makes it possible to forecast and ensure the preset structural, dimensional and physico-mechanical parameters of the materials under study properly. This work can be used for practical low-cost production of highly efficient SiC membranes for micro- and ultrafiltration processes, as well as base for catalysts. [ABSTRACT FROM AUTHOR]

Ceramic materials with excellent radiation resistance stability play an indispensable role in the treatment of nuclear waste. This article uses spark plasma sintering (SPS) to synthesize high-entropy (HE) Y 0.6 Gd 0.6 Sm 0.6 Eu 0.6 Dy 0. 6 Fe 5 O 12 (HEG) and traditional garnet Y 1.2 Nd 1.8 Fe 5 O 12 (YIG). Studied the effects of 2 MeV He2+ irradiation (1 × 1014 ions/cm2 - 1 × 1017 ions/cm2) on the crystal structure, mechanical properties, and chemical stability of ceramics. Research shows that the surface of YIG becomes completely amorphous under ∼30dpa irradiation. Under irradiation at∼30dpa, HEG underwent a small amount of amorphization (with an amorphization rate of 38 %), maintaining the structure of garnet, and the lattice expansion rate of HEG caused by irradiation was lower than that of YIG. After irradiation, the mechanical properties of HEG were improved, while YIG's hardness decreased due to its amorphous state. Radiation has almost no effect on the chemical stability of HEG, and its long-term release mechanism is dominated by diffusion. This study identified HEG as an ideal candidate substrate for immobilizing high-radioactive waste (HLW) the perspective of radiation resistance. [ABSTRACT FROM AUTHOR]

In sophisticated engineering machining, ceramic materials are in great demand in today's precision industries because they have a wide range of potential applications, including automobiles, aircraft, and biomedical engineering. Silicon nitride ceramics (Si3N4) are difficult to manufacture using conventional machining processes. Modern technology allows Ultrasonic Micro-machining (USMM) to create almost any kind of material. Abrasive particles made of silicon carbide are used in this research work to look into the Si3N4 USMM process parameters. The physical structure and chemical composition have been examined in a scanning electron microscope with an integrated energy-dispersive X-ray analyzer. Particle swam optimization and Response Surface Methodology (RSM) desirability were the two types of optimizations used to find the best USMM process parameters. It has been shown that both techniques can be used together to get the best Material Removal Rate (MRR). The best settings were Slurry Concentration: 50 (g/l), Power Rating: 329 (W), and Tool Feed Rate: 1.06 (mm/min). Similarly, to minimize Overcut (OC) and Taper Angle (TA), the ideal method is to use a slurry concentration of 50 (g/l), a power rating of 400 (W), and a tool feed rate of 1.2 (mm/min). Finally, using the RSM, the USMM process was optimized in a way that maximized the MRR while minimizing OC and TA. It was found that the slurry concentration of 42.7 g/l, the power rating of 357.6 W, and the tool feed rate of 1.2 mm/min were the ideal settings for the USMM process. [ABSTRACT FROM AUTHOR]

Advances in vat photopolymerization 3D printing have the potential to significantly improve the production of ceramic materials for electrochemical energy devices. Solid oxide fuel cells (SOFCs) and solid oxide electrolysis cells (SOECs) necessitate high‐resolution ceramic manufacturing methods, as well as precisely controlled porosity (≈20–40%) for optimal gas transport. Achieving a balance between this porosity and mechanical integrity, especially under thermal stress, remains a challenge. Herein, the successful fabrication of porous yttria‐stabilized zirconia (YSZ) ceramics using vat photopolymerization 3D printing is demonstrated, achieving porosities ranging from 6% to 40% and corresponding grain sizes of ≈80–550 nm. It is found that 3D‐printed YSZ with ≈33% porosity exhibited a Weibull modulus of m = 5.3 and a characteristic strength of over 36 MPa. In the investigation, it is further revealed that these ceramics can withstand thermal shock up to 500 °C, retaining over 70% of their flexural strength. This remarkable performance suggests significant potential for 3D‐printed porous YSZ in SOFCs and SOECs, paving the way for potential improved efficiency, reduced fabrication costs, and innovative designs in these next‐generation clean energy technologies. [ABSTRACT FROM AUTHOR]

The mechanical properties of composite ceramic materials obtained based on oxygenfree silicon compounds are largely determined by the properties of the glass binder. This paper presents the results of studies aimed at determining the most fusible glass in the pseudo-binary system 2MgO⋅2Al2O3⋅5SiO2–2MnO⋅2Al2O3⋅5SiO2 with a high tendency to crystallize as a glass-ceramic binder for low-temperature sintering of high-strength ceramic materials based on oxygen-free silicon compounds. The crystallization tendency of the experimental melts decreases with an increase in in the content of manganese cordierite, as confirmed by X-ray and infrared spectroscopic studies. Based on experimental studies, a melting diagram was constructed, which was used to determine the ratio between magnesium cordierite and manganese cordierite (50:50 wt.%), ensuring a minimum melt temperature of 12750 C. The melting point of the glass of the specified composition is 14500 C. The synthesized glass is characterized by a softening point of 8000 C and crystallizes intensively at 10300 C. The The thermal coefficient of linear expansion of the crystallized glass samples is 20.8⋅10–7 0C–1. X-ray diffraction and electron microscopic studies have shown that the developed glass is almost completely crystallized during heat treatment for 2 hours, forming a cordierite solid solution 2(Mg,Mn)O⋅2Al2O3. The size of the cordierite phase crystals ranges from 0.5 to 3.0 µm. Due to its fusibility and high crystallization tendency, the developed glass, can be proposed as a promising glassceramic binder for the production of high-strength ceramic materials (wear and impact resistant) based on SiC and Si2. The size of the cordierite phase crystals ranges from 0.5 to 3.0 µm. Due to its fusibility and high crystallization tendency, the developed glass, can be proposed as a promising glassceramic binder for the production of high-strength ceramic materials (wear and impact resistant) based on SiC and Si3N4 with reduced sintering temperatures. [ABSTRACT FROM AUTHOR]

Esh-Shaheinab is a landmark in the African Neolithic. This site gave the name Shaheinab Neolithic to the Neolithic period in central Sudan, becoming its archetype. Excavated in the late 1940s by A.J. Arkell, it bears witness to the processes of domestic animal introduction from the Middle East into North and East Africa. Its excavation also uncovered the remains of an earlier Mesolithic or Early Khartoum (ca. ninth-sixth millennia BC) and a Late Neolithic occupation (ca. fourth millennium BC), providing essential insights into the Neolithic's premises and sequels. Although the influence of Esh-Shaheinab has been recognized for more than seventy years, our knowledge of its material culture has remained as it was then. In 2001, one of the present authors (EAAG) had permission to restudy the ceramic collection at the National Museum in Khartoum and subsequently export samples for laboratory analyses. Here, for the first time, we provide a multi-scale analysis of the Esh-Shaheinab ceramic material from the Early Khartoum to the Late Neolithic periods by integrating the chaîne opératoire approach into the local landscape. By combining the results of macroscopic and microscopic analyses, we performed petrographic investigations on the composition and manufacturing technology of the ceramic pastes using polarized optical microscopy (POM) and scanning electron microscopy (SEM-EDS). Organic residue analysis (ORA) was also carried out, to provide information on diet, vessel use, and subsistence practices. The results of our combined analyses showed that the inhabitants of Esh-Shaheinab developed an adaptation specific to the ecological niche they inhabited. They lived in the western valley of the Nile, which was narrower and offered different environmental conditions than the eastern bank. This resulted in partial continuity in manufacturing traditions and ceramic recipes, including more mixed wadi materials and a strong emphasis on wild meat consumption as the narrower alluvial plain restricted animal herding. [ABSTRACT FROM AUTHOR]