Microstructure and toughening mechanisms of Al2O3/(W,Ti)C/graphene composite ceramic tool material

To toughen the Al₂O₃ matrix ceramic materials, Al₂O₃/(W, Ti)C/graphene multi-phase composite ceramic materials were fabricated via hot pressing. The effects of the graphene nanoplates (GNPs) content on microstructure and mechanical properties were investigated. Results showed that the fracture toughness and flexural strength of the composite added with just 0.2?wt% GNPs were markedly improved by about 35.3% (~ 7.78?MPa?m^1/2) and 49% (~ 608.54?MPa) respectively compared with the specimens without GNPs while the hardness was kept about 24.22?GPa. However, the mechanical properties degrade with the further increase of GNPs’ content owing to the increased defects caused by agglomeration of GNPs. Synergistic toughening effects of (W, Ti)C and GNPs played an essential role in improving the fracture toughness of composites. By analyzing the microstructures of fractured surface and indentation cracks, besides GNPs pull-out, crack deflection, crack bridging, crack branching and crack arrest, new toughening mechanisms such as break of GNPs and crack guiding were also identified. Furthermore, interface stress can be controlled by means of stagger distributed strong and weak bonding interfaces correlated with the distribution of GNPs.     

The microstructure and mechanical properties of Ni/Al2O3 composites by in-situ generated CaAl12O19 and ZrO2 via hot pressing sintering

Ni/Al₂O₃ composites with a varying mass fraction of CaZrO₃ (0–12 wt%) were prepared by vacuum hot pressing sintering at 1650 °C under a pressure of 30 MPa for 30 min to investigate how CaZrO₃ affect the mechanical properties and morphology of the composites. The results show that CaZrO₃ can react with Al₂O₃ and form new strengthening and reinforcing phases of CaAl₁₂O₁₉ and ZrO₂, which can promote complete densification and solve the problem of uneven distribution due to the poor wettability between Al₂O₃ and Ni. Additionally, composites showed satisfactory mechanical properties when 6.0–9.0 wt% CaZrO3 was added and the major toughening mechanism involved the typical fracture of delamination and the transgranular mode.     

Mechanical performance and microstructure of 3Y-TZP/Al2O3/GNPs medical ceramic surgical scalpel material prepared through SPS–HF dual sintering method

In this study, 3 mol% yttria-stabilized tetragonal zirconia polycrystal (3Y-TZP)/Al₂O₃/graphene nanoplatelets (GNPs) medical ceramic materials for manufacturing surgical scalpels were sintered in vacuum in an SPS–625HF furnace. The mechanical performances and microstructures of the composites were investigated, and the influence mechanisms of the sintering temperature and amount of added GNPs were studied. During the sintering process at 1400°C and 30 MPa for 5 min, the added GNPs enhanced the mechanical properties of the 3Y-TZP/Al₂O₃ composites. The results showed that the composite with .1 wt.% GNPs had 6.4% (910 ± 11 MPa) higher flexural strength than 3Y-TZP/Al₂O₃. The composite with .4 wt.% GNPs had 38.7% (12.95 ± .22 MPa m^1/2) greater fracture toughness than 3Y-TZP/Al₂O₃. The main toughening mechanisms of 3Y-TZP/Al₂O₃/GNPs were crack bridging, crack deflection, crack branching, GNPs bridging, transgranular fracture structures, and phase transformation of t-ZrO_1.95. The two-stage densification displacement curve appeared at the optimal sintering temperature of the materials, and the 3Y-TZP/Al₂O₃/GNPs composites with a two-stage densification displacement curve had excellent mechanical properties. The added GNPs can inhibit the grain growth during the sintering process, thereby refining the zirconia grains. With the increase in GNPs content, the grain size and flexural strength of the composites decreased gradually. However, higher content of GNPs was beneficial to improve the relative density and thermal diffusivity of 3Y-TZP/Al₂O₃/GNPs composite material.     

Role of nano-ZrO2 powder in in-situ formation of ceramic whiskers in Al2O3-C slide plate materials

The effects of nano-ZrO₂ powder on the evolution of phase composition and microstructure of Al₂O₃–C materials during firing have been investigated using tabular alumina, Si powder, Al powder, graphite and nano-ZrO₂ powder as starting materials. The residual content of Al and Si gradually decreased with increasing temperature, and the added nano-ZrO₂ facilitates the reactions involving Si and Al. The quantity of in-situ synthesized AlN and SiC whiskers exhibiting continuous interlocking networks increased gradually with temperature. Nano-ZrO₂ facilitates more ceramic whiskers generated in samples, which play a strengthening and toughening role in the materials, thus improving the thermal shock resistance and high temperature strength of Al₂O₃–C materials. In addition, physical properties are improved due to the nano-ZrO₂ filling the pores and increasing the density of materials.     

Effect of CeO2 and Al2O3 contents on Ce‐ZrO2/Al2O3 composites

Effect of CeO₂ and Al₂O₃ contents on phase composition, microstructures, and mechanical properties of Ce–ZrO₂/Al₂O₃ composites was studied. The CeO₂ content in CeO₂–ZrO₂ varied from 7 to 16 mol%, and the Al₂O₃ content in Ce‐ZrO₂/Al₂O₃ composites were 7 and 22 wt%. When CeO₂ content was ≤10 mol%, high Al₂O₃ content contributed to hinder the tetragonal‐to‐monoclinic ZrO₂ phase transformation during cooling and decrease the density of microcracks in the composites. Tetragonal ZrO₂ single‐phase was obtained in the composites with ≥12 mol% CeO₂, regardless of the Al₂O₃ content. Hardness, flexural strength, and toughness were dependent on CeO₂ and Al₂O₃ contents which were related to the microcracks, grain size, and phase transformation. The high flexural strength and toughness of the composites with 7wt% Al₂O₃ could be obtained at an optimum CeO₂ content of 12 mol%, whereas those of the composites with 22 wt% Al₂O₃ could be achieved in the wide CeO₂ content range of 8.5‐12 mol%.     

Microstructure and improved mechanical properties of Al2O3/Ba-β-Al2O3/ZrO2 composites with YSZ addition

Al₂O₃/Ba-β-Al₂O₃/ZrO₂ composites were fabricated by solid-state reaction sintering of Al₂O₃, BaZrO₃, and yttria stabilized zirconia (YSZ) powders. The effects of YSZ addition on microstructure and mechanical properties have been investigated. The incorporation of YSZ promoted the densification of the composites and formation of tetragonal ZrO₂ phase. The microstructure of the composites was characterized by elongated Ba-β-Al₂O₃ phase and equiaxed ZrO₂ particles including added YSZ and reaction-formed ZrO₂. The Al₂O₃/Ba-β-Al₂O₃/ZrO₂ composites with YSZ addition exhibited improved fracture toughness, as a result of multiple toughening effects including crack deflection, crack bridging, crack branching, and martensitic transformation of ZrO₂ formed by the reactions between Al₂O₃ and BaZrO₃. Moreover, owing to the grain refinement of Al₂O₃ matrix, dispersion strengthening of the added YSZ particles, and an increase in density of the composites, the Vickers hardness and flexural strength of Al₂O₃/Ba-β-Al₂O₃/ZrO₂ composites were dramatically enhanced in comparison with the composites without YSZ addition.     

Fabrication and mechanical properties of Al2O3–TiC ceramic composites synergistically reinforced with multi-walled carbon nanotubes and graphene nanoplates

In this study, Al₂O₃–TiC composites synergistically reinforced with multi-walled carbon nanotubes (MWCNTs) and graphene nanoplates (GNPs) were prepared via spark plasma sintering (SPS). The effects of the MWCNT and GNP contents on the phase composition, mechanical properties, fracture mode, and toughening mechanism of the composites were systematically investigated. The experimental results indicated that the composite grains became more refined with the addition of MWCNTs and GNPs. The nanocomposites presented high compactness and excellent mechanical properties. The composite with 0.8 wt% MWCNTs and 0.2 wt% GNPs presented the best properties of all analysed specimens, and its relative density, hardness, and fracture toughness were 97.3%, 18.38 ± 0.6 GPa, and 9.40 ± 1.6 MPa m^1/2, respectively. The crack deflection, bridging, branching, and drawing effects of MWCNTs and GNPs were the main toughening mechanisms of Al₂O₃–TiC composites synergistically reinforced with MWCNTs and GNPs.     

Effects of ZrO2 nanoparticles on the microstructure and mechanical properties of ZrO2/AlSi10Mg composites manufactured by laser powder bed fusion

In this work, the nano-ZrO₂ particles were mixed into AlSi10Mg alloy to prepare ZrO₂/AlSi10Mg composites with different x wt.% ZrO₂ (x = 0, 0.15, 0.3, 0.45, 0.6, 0.75). The microstructure, mechanical properties and the anisotropy of the ZrO₂/AlSi10Mg composites fabricated by laser powder bed fusion (LPBF) were studied. The results show that nano-ZrO₂ particles can be uniformly dispersed on the AlSi10Mg powder by the method of pre-dispersion and mechanical mixing. When the mass ratio of ZrO₂ in ZrO₂/AlSi10Mg composites is 0.3 wt%, the values of the tensile strength, yield strength and elongation are 493.64 MPa, 321.30 MPa and 11.74%, respectively. Compared with AlSi10Mg alloy, the tensile strength of ZrO₂/AlSi10Mg composites with 0.3 wt% is increased by 30–55 MPa and the elongation is increased by 3–5%. In addition, the mechanical properties of AlSi10Mg alloy and ZrO₂/AlSi10Mg composites of 0.3 wt% exhibit antistrophic behavior in different direction, which is due to the differences of microstructure, texture and stress distribution between transverse direction (TD) and build direction (BD). Compared with other AlSi10Mg matrix composites, ZrO₂/AlSi10Mg composites of this work show excellent strength and plasticity matching.     

Comparison of sintering behavior and reinforcing mechanisms between 3Y-TZP/Al2O3(w) and 12Ce-TZP/Al2O3(w) composites: Combined effects of lanthanide stabilizer and Al2O3 whisker length

The densification behavior, microstructural development, toughening and strengthening mechanisms of Al₂O₃ whisker-reinforced 3Y-TZP and 12Ce-TZP composites were systematically and comparatively investigated with varying whisker lengths. Compared with 3Y-TZP/A_w composites, the presence of a Ce-Al-Si-O amorphous phase, caused by the addition of Al₂O₃ whiskers, promoted the densification and grain growth of 12Ce-TZP/A_w composites. Crack deflection and bridging are proposed as the primary toughening mechanisms for 3Y-TZP/A_w composites, while the t-m martensitic transformation would dominate the toughening and strengthening processes of 12Ce-TZP/A_w composites. Changes in Al₂O₃ whisker length would vary the distributions of internal stress and amorphous phase within the ceria-stabilized ZrO₂ matrix, and hence affect the toughening and strengthening results. It indicates that effective toughening and strengthening of the Al₂O₃ whisker-reinforced TZP composites can be achieved by taking advantage of collaborative engineering control on the reinforcement morphology and the interface chemistry/structure.     

Effect of Y2O3-stabilized ZrO2 whiskers on the microstructure,mechanical and wear resistance properties of Al2O3 based ceramic composites

The aim of this study was to improve the mechanical properties of Al₂O₃ ceramics by the addition of Y₂O₃-stabilized ZrO₂ whiskers (designated as Al₂O₃/YSZ_W composite) through the flux method and hot-pressing technology. The effect of YSZ_W content on their microstructure, phase composition and transformability, mechanical properties, and wear resistance was systematically investigated. The Al₂O₃/YSZ_W composites containing 10 wt% YSZ_W exhibited the best mechanical performance, including the highest content of YSZ_W tetragonal phase and transformability as well as the largest values in their relative density (99.5%), hardness (1969 HV), fracture toughness (9.57 MPa m^1/2) and flexural strength (855 MPa). The strengthening and toughening of the Al₂O₃/YSZ_W composites were attributed to the YSZ_W tetragonal-monoclinic phase transformation as well as the whiskers reinforcing effect. Furthermore, the Al₂O₃/YSZ_W composites also showed the highest friction and wearing properties.     

The microstructure,formation mechanism and sintering characteristics of Al2O3/ZrO2 supersaturated solid solution powders

In this study, the Al₂O₃/ZrO₂ supersaturated solid solution powders with different ZrO₂ contents were successfully synthesized by a novel combustion synthesis combined with water cooling (CS-WC) method. The solid solubility and formation mechanism of solid solution under the extremely non-equilibrium solidification condition were discussed in details. The ultra-high cooling rate greatly improves the solubility limit of Al₂O₃ in ZrO₂. When ZrO₂ content is 30 mol%, the Al₂O₃ has been almost dissolved into the ZrO₂ lattice. The formation mechanism of solid solution can be attributed to solute interception caused by the huge degree of supercooling. During the sintering process, the solid solution powders precipitate ZrO₂ particles and the Al₂O₃ matrix, which forms a fine and uniform nanostructure. Due to the synergistic effect of t-m phase transformation toughening and ZrO₂ nanoparticles toughening, the Al₂O₃/ZrO₂ nanoceramics exhibit excellent mechanical properties when ZrO₂ contents are at the range of 25–37 mol%.     

Role of CeAl11O18 in reinforcing Al2O3/Ti composites by adding CeO2

This work discusses the reinforcement effect of elongated CeAl₁₁O₁₈ phase on multifunctional Al₂O₃/Ti composites by adding CeO₂ to inhibit interfacial reaction and strengthen interface for inducing optimized performances. For this purpose, Al₂O₃/Ti composite with different contents of CeO₂ was fabricated and the microstructure, mechanical and electrical properties were studied. Results indicated that after CeO₂ was added, elongated CeAl₁₁O₁₈ phase was formed within these composites. Owing to inhibited interfacial reaction between Al₂O₃ and Ti, Ti content was increased and compositions of composites were calculated using Rietveld method based on X-ray diffraction patterns. Attributed to the strengthening and toughening effects of CeAl₁₁O₁₈ phase, 2 mol% CeO₂ added composite showed the highest flexural strength and fracture toughness of 576 MPa and 5.15 MPa·m^1/2, which increased by 21% and 20% compared to Al₂O₃/Ti composite without CeO₂ addition. In this case, crack bridging by both Ti and CeAl₁₁O₁₈ particles was the major toughening mechanism and the additional fracture toughness caused by CeAl₁₁O₁₈ toughening effect reached a maximum. The role (crack bridging or particle pull-out mechanism) of CeAl₁₁O₁₈ in toughening Al₂O₃/Ti composites depended on the aspect ratio of these elongated particles, which was directly related to CeO₂ content. Because of the inhibition of interfacial reaction and the increase in Ti content, excellent electrical resistivity of composites after CeO₂ addition was maintained in spite of the formation of insulated CeAl₁₁O₁₈ phase. All samples showed relatively low electrical resistivity of ~10⁻³ Ωcm.     

Reaction mechanisms and properties of in situ porous Al2O3-ZrO2-mullite composites

Customized porous Al₂O₃-ZrO₂-mullite composites were designed and prepared by reaction sintering of zircon (ZrSiO₄) and alumina (Al₂O₃) at sintering temperatures from 1400 to 1600 °C for 3 h. The mechanical properties, microstructural evolution, and reaction mechanisms of the composites were investigated. The reactions between ZrSiO₄ and Al₂O₃ were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectrometer (EDS). The results indicate that ZrSiO₄ and Al₂O₃ react and form ZrO₂ and mullite. Sintering temperature has an important effect on the reaction process. At 1400 °C, Al₂O₃ reacts directly with SiO₂ of ZrSiO₄ to form mullite and ZrO₂, which reduces the decomposition temperature of ZrSiO₄ and promotes the decomposition of ZrSiO₄. However, at 1600 °C, ZrSiO₄ first decomposes to form SiO₂ and ZrO₂, and then generates mullite by the diffusion of Si. The migration of Si is the key factor for the formation of mullite. The thermal shock resistance of the composites can be significantly improved by phase transformation toughening of in-situ ZrO₂. Therefore, increasing the proportion of ZrSiO₄ can significantly improve the mechanical properties of sample. The residual ratio of the flexural strength after thermal shock exceeded 90%, when the mass ratio of ZrSiO₄ to Al₂O₃ was 3:1. Besides, the addition of polymethyl methacrylate could improve the porosity of materials and has a direct effect on the thermal conductivity of composites.     

A comparative study of thermal conductivity and thermal emissivity of high temperature solar absorber of ZrO2 /Fe2O3 and Al2O3/CuO ceramics

Oxide ceramics are considered as promising high temperature solar absorber materials. The major aim of this work is the development of a new solar absorber material with promising characteristics, high efficiency and low-cost processing. Hence, this work provides a comparative and inclusive study of densification behavior, microstructure features, thermal emissivity and thermal conductivity values of the two new high temperature solar absorbers of ZrO₂/Fe₂O₃ and Al₂O₃/CuO ceramics. Ceramic composites of ZrO₂/(10–30 wt%) Fe₂O₃ and Al₂O₃/(10–30 wt%) CuO were prepared by pressureless sintering method at a temperature of 1700 °C/2hrs. Identification of the solar to thermal efficiency of the composites was evaluated in terms of their measured thermal emissivity. Thermal efficiency and heat transfer homogeneity were investigated in terms of thermal conductivity and diffusivity measurement. The results showed that both composites exhibited comparable densification behavior, homogenous and harmonious microstructure. However, Al₂O₃/10 wt% CuO composite showed higher thermal and solar to thermal efficiencies than ZrO₂/Fe₂O₃ composites. It gave the lowest and the best thermal emissivity of 0.561 and the highest thermal conductivity of 15.4 W/m. K. These values proved to be the best amongst all those of the most known solar absorber materials made from the expensive SiC and AlN ceramics. Thus, Al₂O₃/CuO composites have succeeded in obtaining outstanding properties at a much lower price than its other competitive materials. These results may strongly identify Al₂O₃/CuO composites as promising high-temperature solar absorber materials instead of ZrO₂ and the other carbide and nitride ceramics.     

Grain growth kinetics in microwave sintered graphene platelets reinforced ZrO2/Al2O3 composites

The grain growth kinetics and mechanical properties of graphene platelets(GPLs) reinforced ZrO₂/Al₂O₃(ZTA) composites prepared by microwave sintering were investigated. The calculated grain growth kinetics exponent n indicated that the GPLs could accelerate the process of the Al₂O₃ columnar crystal growth. And the grain growth activation energy of the Al₂O₃ columnar crystal indicated that the grain growth activation energy of the GPLs doped ZTA composites is much higher than those of pure Al₂O₃ and ZTA in microwave sintering. The optimal mechanical properties were achieved with 0.4?vol% GPLs, whose relative density, Vickers hardness and fracture toughness were 98.76%, 18.10?GPa and 8.86?MPa?m^1/2, respectively. The toughening mechanisms were crack deflection, bridging, branching and pull-out of GPLs. The results suggested that GPLs-doped are good for the Al₂O₃ columnar crystal growth in the ZTA ceramic and have a potentially improvement for the fracture toughness of the ceramics.     

Synergistic thermal conductivity enhancement of PC/ABS composites containing alumina/magnesia/graphene nanoplatelets

Graphene nanoplatelets (GNPs) have attracted considerable attention in the field of thermal management materials due to their unique structure and exceptional thermal conductive properties. In this work, we demonstrate a significant synergistic effect of GNPs, alumina (Al₂O₃), and magnesia (MgO) in improving the thermal conductivity of polycarbonate/acrylonitrile‐butadiene‐styrene polymer alloy (PC/ABS) composites. The thermal conductivity of the composites prepared through partial replacement of Al₂O₃ and MgO with GNPs could increase dramatically compared with that without GNPs. The maximum thermal conductivity of the composite is 3.11 W mK⁻¹ at total mass fraction of 70% with 0.5 wt% GNPs loading. It increases 60% compared with that without GNPs (1.95 W mK⁻¹). The synergistic effect results from the compact packing structure formed by Al₂O₃/MgO and the bridging of GNPs with Al₂O₃/MgO, thus promoting the formation of effective thermal conduction pathways within PC/ABS matrix. More importantly, together with the intrinsically high thermal conductivity of GNPs, boosted and effective pathways for phonon transport can be created, thus decrease the thermal resistance at the interface between fillers and PC/ABS matrix and increase the thermal conductivity of composites. POLYM. COMPOS., 38:2221–2227, 2017. © 2015 Society of Plastics Engineers     

CNT-induced TiC toughened Al2O3/Ti composites: Mechanical,electrical, and room-temperature crack-healing behaviors

This study addressed novel multiphase composite of Al₂O₃/Ti/TiC that exhibited enhanced fracture toughness and room-temperature crack-healing function. Al₂O₃/Ti/TiC composites were fabricated through hot-press sintering of CNT, TiH_2, and Al₂O₃ mixed powders, where the TiC was in-situ formed by reaction of CNT and Ti. The effects of CNT (TiC) content on mechanical and electrical properties were studied. Electrochemical anodization process at room temperature was attempted to these composites to heal cracks introduced in the surface of composites. Results indicated that added CNT was invisible while metal Ti and reaction product TiC coexisted in all samples. The reaction between CNT and Ti[O] representing dissolved active oxygen into Ti was considered as the main formation route of TiC. The toughening mechanism was demonstrated as crack deflection and bridging due to the presence of TiC. In spite of the increase in electrical resistivity because of the higher resistivity of TiC than Ti, the present Al₂O₃/Ti/TiC composites still remain high enough electrical conductivity (8.0 × 10⁻³ Ωcm ~1.8 × 10⁻² Ωcm for 0-2 vol% CNT addition) which could be regarded as conductors; it allowed to heal cracks in the composites by electrochemical anodization that formed titanium dioxide phase at room temperature. It was found that crack-healing ability in 1 vol% CNT added composite exhibited higher strength recovery ratio of 95.6% to the crack-free sample than that of Al₂O₃/Ti composite (the recovery ratio of 89.6%). After crack-healing process, mechanical strength of samples increased by 52.3% compared to cracked composites. It was concluded that the formed TiC could contribute to the appropriate electrical conduction as well as interface strengthening in the Al₂O₃/Ti composites. Furthermore, it was firstly speculated that the TiC could be electrochemically anodized to form an oxide like Ti metal. These characteristics enable Al₂O₃/Ti/TiC composites as the crack-healing materials at room temperature.     

Fabrication and mechanical properties of short ZrO2 fiber reinforced NiFe2O4 matrix composites

Short ZrO₂ fibers (ZrO_2(f)) reinforced NiFe₂O₄ ceramic composites were fabricated by cold pressing process. The phase composition, microstructure, mechanical properties and fiber/matrix interface of the composites were investigated by X-ray diffraction, scanning electron microscopy and mechanical testing machines. ZrO_2(f) show good thermodynamic and chemical compatibility with NiFe₂O₄ ceramic matrix and effectively enhanced the mechanical properties. The toughening mechanisms are fiber bridging, interfacial debonding, fiber pullout, phase transformation and the matrix constraint effect. By incorporation of 3 wt% fibers with the average length of 5～6 mm, the bending strength and fracture toughness of the composites reached 88.92 MPa and 4.62 MPa m^1/2, respectively, while the strength conservation ratio after thermal shock increased from 48.85% to 75.86%. The weak interface bonding built up between ZrO_2(f) and NiFe₂O₄ facilitates the reinforcing effects of the fibers to operate.     

Synthesis and characterization of Al2O3-TiC-ZrO2 ceramics with intragranular nanostructure by spark plasma sintering

In this paper, Al₂O₃-TiC ceramic composites with intragranular nano-ZrO₂ were prepared in vacuum by spark plasma sintering (SPS). The effect of ZrO₂ particles with different nano-sizes on the microstructure and mechanical properties of ceramics was studied. The results show that SPS can achieve relative densification of materials without generating new impurity phases. At the same time, the sintering densification temperature of ceramic materials can be reduced by adding ZrO₂ (20 nm) particles. Under the action of SPS strong electric field, the nano-ZrO₂ adsorbed on the surface of the matrix particles can enter the interior of matrix grains, and form intragranular nanostructures when the grain boundaries move and the particles merge. The microstructure and mechanical properties of ceramic materials can be improved through the intragranular structure formed by nanoparticles. The main reasons for the increased strength and toughness of ceramic materials are crack deflection, crack bridging and transgranular fracture.     

Properties and microstructural aspects of TiO2‐doped sintered Alumina‐Zirconia composite ceramics

The effect of titania content on the densification, the phase transformation, the microstructures, and mechanical properties of 50 wt% Al₂O₃‐50 wt% ZrO₂ (12 mol% CeO₂) was evaluated. Ceramic composites with different TiO₂ content (0.27, 5, 10 wt%) were prepared by pressureless sintering at low temperature (1400°C) for 2 hours in air. Dense ceramic was obtained by adding 5 wt% of TiO₂ loading to improved mechanical properties. The microstructure analysis provided lots of information about solid‐state reactivity in alumina‐zirconia‐titania ternary system. The content of TiO₂ strongly affected the phases evolution and the grain growth during sintering. Furthermore, a significant effect on mechanical properties and fracture behavior was also observed.