The effect of calcination temperature on the structural properties and phase formation of synthesized CaO-Al₂O₃ nanopowder was investigated and discussed. The calcination products were identified by differential thermal analysis (DTA) and the crystalline phase formation was analyzed by X-ray diffraction (XRD). The obtained results showed that the crystallization started at 460 °C. Finally, the microstructures of the nanoparticles were observed by scanning (SEM) and transmission electron (TEM) microscopes. The investigation showed that an increase in the calcination temperature led to the appreciable increase in the crystallite size and the crystallinity of the final product. The obtained data confirmed that the prepared materials were mayenite with different surface area in the range of 71.18 m²/g to 10.34 m²/g after annealing in the temperature range of 470 °C to 960 °C.

Titanium boride (TiB₂) is a material classified as an ultra-high-temperature ceramic. The TiB₂ structure is dominated by covalent bonds, which gives the materials based on TiB₂ very good mechanical and thermal properties, making them difficult to sinter at the same time. Obtaining dense TiB₂ polycrystals requires a chemical or physical sintering activation. Carbon and molybdenum disilicide (MoSi₂) were chosen as sintering activation additives. Three series of samples were made, the first one with carbon additives: 0 to 4 wt.%; the second used 2.5, 5 and 10 wt.% MoSi₂; and the third with both additions of 2 wt.% carbon and 2.5, 5 and 10 wt.% MoSi₂. On the basis of the dilatometric sintering analysis, all additives were found to have a favourable effect on the sinterability of TiB₂, and it was determined that sintering TiB₂ with the addition of carbon can be carried at 2100 °C and with MoSi₂ and both additives at 1800 °C. The polycrystals were sintered using the hot-pressing technique. On the basis of the studies conducted in this work, it was found that the addition of 1 wt.% of carbon allows single-phase TiB₂ polycrystals of high density (>90%) to be obtained. The minimum MoSi₂ addition, required to obtain dense sinters with a cermet-like microstructure, was 5 wt.%. High density was also achieved by the materials containing both additives. The samples with higher MoSi₂ content, i.e., 5 and 10%, showed densities close to 100%. The mechanical properties, such as Young’s modulus, hardness and fracture toughness (K_Ic), of the polycrystals and composites were similar for samples with densities exceeding 95%. The Vickers hardness was 23 to 27 GPa, fracture toughness (K_IC) was 4 to 6 MPa·m^0.5 and the Young’s modulus was 480 to 540 GPa. The resulting TiB₂-based materials showed potential in high-temperature applications.

ZrB₂-HfB₂ composites allow us to obtain materials characterized by the high chemical resistance characteristic of HfB₂ while reducing density and improving sinterability due to the presence of ZrB₂. Since boride composites are difficult-to-sinter materials. One way to achieve high density during sintering is to add phases that activate mass transport processes and, after sintering, remain as composite components that do not degrade and even improve some properties of the borides. The following paper is a comprehensive review of the effects of various and the most commonly used sintering aids, i.e., SiC, B₄C, WC, MoSi₂, and CrSi₂, on the thermo-chemical properties of the ZrB₂-HfB₂ composites. High-density composites with a complex phase composition dominated by (Zr,Hf)B₂ solid solutions were obtained using a hot pressing method. The tests showed differences in the properties of the composites due to the type of sintering additives used. From the point of view of the thermo-chemical properties, the best additive was silicon carbide. The composites containing SiC, when compared to the initial, pure borides, were characterized by high thermal conductivity λ (80–150 W/m·K at 20–1000 °C), a significantly reduced thermal expansion coefficient (CTE ~6.20 × 10⁻⁶ 1/K at 20–1000 °C), and considerably improved oxidation resistance (up to 1400 °C).

Titanium boride (TiB2) is a material classified as ultra-high temperature ceramics. The TiB2 structure is dominated by covalent bonds, which gives materials based on TiB2 very good mechanical and thermal properties, but also makes them difficult to sinter. Obtaining dense TiB2 polycrystals requires chemical or physical sintering activation. Carbon and molybdenum disilicide (MoSi2) were chosen as sintering activation additives. Three series of samples were made, the first with carbon additives: 0 to 4 wt.%; the second with 2.5, 5 and 10 wt.%. MoSi2 and the third with both additions of 2 wt.% carbon and 2.5, 5 and 10 wt.% MoSi2. MoSi2. On the basis of dilatometric sintering analysis, all additives were found to have a favourable effect on sinterability of TiB2, and it was determined that sintering of TiB2 with carbon addition can be carried at 2100°C and with MoSi2 and both additives at 1800°C. The polycrystals were sintered using the hot pressing technique. On the basis of the studies conducted in this work, it was found that addition of 1 wt.% of carbon allows to obtain single-phase TiB2 polycrystals of high density (>90%). The minimum MoSi2 addition required to obtain dense sinters with a cermet-like microstructure was 5 wt.%. High density was also achieved by materials containing both additives. Samples with higher MoSi2 content, i.e. 5 and 10% showed densities close to 100%. Mechanical properties such; as Young's modulus, hardness and fracture toughness (KIc) of the polycrystals and composites were similar for samples with densities exceeding 95%. The Vickers hardness was 23 to 27 GPa, the fracture toughness (KIC) was 4 to 6 MPa·m0.5 and the Young's modulus was 480 to 540 GPa. The resulting TiB2-based materials showed potential in high-temperature applications.

In this study, bioceramic composites based on zirconia (ZrO₂) were synthesized and characterized in terms of mechanical properties. Two types of different-sized grains of zirconia powders were used to prepare the composites. A commercial zirconia micropowder (Tosoh) was used as a base for the composites modified with bioactive glass (BG), copper-doped bioactive glass (BGCu), and hexagonal boron nitride (hBN) with a sintering temperature of 1450 °C. The composites with the addition of hydroxyapatite, for which their sintering temperature was 1150 °C, were independently fabricated using a zirconia nanopowder prepared via co-precipitation and hydrothermal methods to achieve high densification and avoid hydroxyapatite decomposition. Mechanical performance of these composites was assessed with regard to biaxial flexural strength, Vickers hardness (HV), and fracture toughness (K_Ic). The reference 3Y-TZP material exhibited Vickers hardness (11.8 GPa) and fracture toughness (6.1 MPa∙m^1/2 values typical for dense tetragonal zirconia ceramics. The addition of all bioactive phases resulted in significant alterations in mechanical properties. Specifically, incorporating 20 wt.% HAp led to a threefold decrease in hardness and a 40% reduction in fracture toughness, while increasing the HAp content to 40 wt.% further reduced these properties. Nonetheless, the fracture toughness of these composites remained higher than that of pure hydroxyapatite materials. The incorporation of BG and BGCu reduced the hardness values by 45% and 30%, respectively, compared to 3Y-TZP. The most significant deterioration of the properties was observed for the 3Y-TZP-hBN composite. The 3Y-TZP–BGCu composite exhibited fracture toughness (5.9 MPa∙m^1/2) representing 95% of the toughness of pure zirconium dioxide, thereby showing the lowest weakness of all the other composites with bioactive additives. A slightly lower fracture toughness value (5.3 MPa∙m^1/2) was also observed in the composite with bioglass but lacking the copper additive. This factor, combined with a relatively small decrease in hardness in both cases, highlights high durability for implantology applications, thus marking the indicated materials the most promising among the composites studied.