Microstructures and material properties of fibrous HAp/Al2O3–ZrO2 composites fabricated by multi-pass extrusion process

Fibrous HAp/Al₂O₃–ZrO₂ composites were fabricated using the multi-pass extrusion process. In the 3rd and 4th passed extrusion bodies, fibrous microstructures were obtained. The 3rd and 4th passed Al₂O₃–ZrO₂ cores used as reinforcement, were about 35 and 4.5 μm in diameter, respectively. In the bodies sintered at over 1400 °C, the HAp decomposed and was transformed to β-TCP and TTCP, in which large numbers of pores were observed. The values of bending strength, Vickers hardness and fracture toughness of the 3rd passed HAp/Al₂O₃–ZrO₂ composites were 178 MPa, 325 Hv, and 3.4 MPa m^1/2, respectively while the values of the 4th passed bodies were 190 MPa, 405 Hv and 3.8 MPa m^1/2.     

Microstructure of the directionally solidified ternary eutectic ceramic Al2O3/MgAl2O4/ZrO2

The directionally solidified Al₂O₃/MgAl₂O₄/ZrO₂ ternary eutectic ceramic was prepared via induction heating zone melting. Smooth Al₂O₃/MgAl₂O₄/ZrO₂ eutectic ceramic rods with diameters of 10 mm were successfully obtained. The results demonstrate that the eutectic rods consist of Al₂O₃, MgAl₂O₄ and ZrO₂ phases. In the eutectic microstructure, the MgAl₂O₄ and Al₂O₃ phases form the matrix, the ZrO₂ phase with a fibre or shuttle shape is embedded in the matrix, and a quasi-regular eutectic microstructure formed, presenting a typical in situ composite pattern. During the eutectic growth, the ZrO₂ phase grew on non-faceted phases ahead of the matrix growing on the faceted phase. The hardness and fracture toughness of the eutectic ceramics reached 12 GPa and 6.1 MPa·m ^1/2, respectively, i.e., two times and 1.7 times the values of the pre-sintered ceramic, respectively. In addition, the ZrO₂ phase in the matrix reinforced the matrix, acting as crystal whiskers to reinforce the sintered ceramic.     

Synthesis and characterization of a MgO-MgAl2O4-ZrO2 composite with a continuous network microstructure

Using analytically pure MgO, analytically pure Al₂O₃ and analytically pure ZrO₂ as raw materials, Mg_4.68Al_2.64Zr_1.68O₁₂ was prepared at 1993 K for 10 h, and then, a MgO-MgAl₂O₄-ZrO₂ composite with a continuous network was successfully obtained by controlling the cooling rate based on the in-situ decomposition reaction of Mg_4.68Al_2.64Zr_1.68O₁₂ at temperatures below 1887 K. The three phases of MgO, MgAl₂O₄ and ZrO₂ are highly dispersed in this continuous network microstructure, with ZrO₂ intertwined by MgO and MgAl₂O₄ and micropores with a size of less than 2 µm. Furthermore, the synthesis mechanism of Mg_4.68Al_2.64Zr_1.68O₁₂ is given as follows: first, MgAl₂O₄ is synthesized using the reaction: MgO(s)+Al₂O₃(s)=MgAl₂O₄(s) at temperatures below 1894 K; and then, Mg_4.68Al_2.64Zr_1.68O₁₂ is further prepared through MgO and ZrO₂ diffusion and dissolution into MgAl₂O₄ at temperatures above 1894 K, for example, at 1923 K or 1993 K in this work.     

Sintering,microstructure and mechanical properties of Al2O3–Y2O3–ZrO2 (AYZ) eutectic composition ceramic microcomposites

We report on how the mechanical properties of sintered ceramics (i.e., a random mixture of equiaxed grains) with the Al₂O₃–Y₂O₃–ZrO₂ eutectic composition compare with those of rapidly or directionally solidified Al₂O₃–Y₂O₃–ZrO₂ eutectic melts. Ceramic microcomposites with the Al₂O₃–Y₂O₃–ZrO₂ eutectic composition were fabricated by sintering in air at 1400–1500 °C, or hot pressing at 1300–1400 °C. Fully dense, three phase composites of Al₂O₃, Y₂O₃-stabilized ZrO₂ and YAG with grain sizes ranging from 0.4 to 0.8 μm were obtained. The grain size of the three phases was controlled by the size of the initial powders. Annealing at 1500 °C for 96 h resulted in grain sizes of 0.5–1.8 μm. The finest scale microcomposite had a maximum hardness of 19 GPa and a four-point bend strength of 282 MPa. The fracture toughness, as determined by Vickers indentation and indented four-point bending methods, ranged from 2.3 to 4.7 MPa m^1/2. Although strengths and fracture toughnesses are lower than some directionally or rapidly solidified eutectic composites, the intergranular fracture patterns in the sintered ceramic suggest that ceramic microcomposites have the potential to be tailored to yield stronger, tougher composites that may be comparable with melt solidified eutectic composites.     

Effect of mechanical properties on the ballistic resistance capability of Al2O3-ZrO2 functionally graded materials

Because Al₂O₃ exhibits high strength and hardness, it is prevalently used as a ceramic material. ZrO₂ is often added to increase the toughness of such a material. Therefore, this study mixed Al₂O₃ and ZrO₂ to formulate functionally graded materials (FGMs). four-layer and eleven-layer Al₂O₃-ZrO₂ FGM_S were produced from Al₂O₃ and ZrO₂ mixtures by sintering at 1500 °C. Moreover, testing sheets were created by mixing various ratios of Al₂O₃ and ZrO₂ to analyze their fracture toughness and hardness. The results revealed the 90% Al₂O₃-10% ZrO₂ sheet to exhibit a hardness of 15.12 GPa, and the 50% Al₂O₃-50% ZrO₂ sheet to attain a fracture toughness as high as 4.7 MPa m^0.5. The impact resistance test involved analyzing various types of testing sheets, including the four-layer Al₂O₃-(0%, 10%, 20%, 30%) ZrO₂ FGM, eleven-layer Al₂O₃-(0–100%) ZrO₂ FGM, 100% Al₂O₃ composite material, 90% Al₂O₃-10% ZrO₂ composite material, 70% Al₂O₃-30% ZrO₂ composite material, and 50% Al₂O₃-50% ZrO₂ composite material. The ballistic tests showed that FGMs of the same areal density (4.64 g/cm²) or thickness (11 mm) attained the highest energy absorption. The experimental results confirmed that FGMs can delay the formation and propagation of ceramic cones. Specifically, toughened alumina materials prevent the growth of radial and circumferential cracks, delay the formation of ceramic cones, decrease cones hitting against the back plane, and increase the penetrating resistant capability of the ceramic materials experiencing bullet impact, features important for applications in fields such as aerospace, aviation, automobile, the military industry, and biomedicine     

Mechanical properties and cytotoxicity of 3Y-TZP bioceramics reinforced with Al2O3 particles

The influence of Al₂O₃ addition and sintering parameters on the mechanical properties and cytotoxicity of tetragonal ZrO₂–3 mol% Y₂O₃ ceramics was evaluated. Samples containing 0, 10, 20 and 30 wt.% of Al₂O₃ particles were prepared by cold uniaxial pressing (80 MPa) and sintered in air at 1500, 1550 and 1600 °C for 120 min. The effects of the sintering conditions on the microstructure were analyzed by X-ray diffraction analysis and scanning electron microscopy. Hardness and fracture toughness were determined by the Vickers indentation method and the mechanical resistance by four-point bending tests. As a preliminary biological evaluation, “in vitro” cytotoxicity tests were realized to determine the cytotoxic level of the ZrO₂–Al₂O₃ composites, using the neutral red uptake method with NCTC clones L929 from the American Type Culture Collection (ATCC) bank. Fully dense ceramic materials were obtained with a hardness ranging between 1340 HV and 1585 HV, depending on the amount of Al₂O₃ in the ZrO₂ matrix. On the other hand, no significant influence of the Al₂O₃ addition on fracture toughness was observed, exhibiting values near 8 MPa m^1/2 for all compositions and sintering conditions studied. The non-cytotoxic behavior, the elevated fracture toughness, the good bending strength (σ_f = 690 MPa) and the elevated Weibull's modulus (m = 11) exhibited by the material, show that these ceramic composites are highly suitable biomaterials for dental implant applications.     

Phase diagram of the Al2O3–ZrO2–La2O3 system

The phase diagram of the Al₂O₃–ZrO₂–La₂O₃ system was constructed in the temperature range 1250–2800 °C. The liquidus surface of the phase diagram reflects the preferentially eutectic interaction in the system. Three new ternary and two new binary eutectics were found. The minimum melting temperature is 1665 °C and it corresponds to the ternary eutectic LaAlO₃ + T-ZrO₂ +  La₂O₃·11Al₂O₃. The solidus surface projection and the schematic of the alloy crystallization path confirm the preferentially congruent character of phase interaction in the ternary system. The polythermal sections present the complete phase diagram of the Al₂O₃–ZrO₂–La₂O₃ system. No ternary compounds or regions of remarkable solid solution were found in the components or binaries in this ternary system. The latter fact is the theoretical basis for creating new composite ceramics with favorable properties in the Al₂O₃–ZrO₂–La₂O₃ system.     

Microstructure and mechanical properties of Al2O3/Y3Al5O12/ZrO2 hypereutectic directionally solidified ceramic prepared by laser floating zone

Al₂O₃/Y₃Al₅O₁₂/ZrO₂ directionally solidified ceramic has been considered as a promising candidate for ultrahigh temperature structural materials due to its excellent performance even close to its melting point. In this work, laser floating zone (LFZ) solidification experiments were performed on Al₂O₃/Y₃Al₅O₁₂/ZrO₂ hypereutectic with the solidification rates between 2 μm/s and 30 μm/s. The full eutectic lamellar microstructure is obtained with hypereutectic composition. The solid/liquid interface morphology is investigated. The microstructure characteristic is discussed based on the solid/liquid interface. The variation of lamellar spacing with different compositions and solidification rates was reported and discussed by considering an irregular eutectic growth model. The maximum hardness and fracture toughness are 19.06 GPa and 3.8 MPa m^1/2, respectively. The toughening mechanism of ZrO₂ is discussed based on the scenario of the crack propagation pattern.     

Reaction and phases from monoclinic zirconia and calcium aluminate cement at high temperatures

Solid state reaction using m-ZrO₂ and high alumina cement as starting materials was studied. Various compositions containing different proportions of calcium aluminate cement (5–50 mol% CaO in ZrO₂) were reaction sintered at 1300–1500 °C. Crystalline phase formation and densification of Ca stabilized ZrO₂ composites was investigated by X-ray diffraction analysis, density and shrinkage measurements. Scanning electron microscopy (SEM) combined with energy dispersive X-ray spectroscopy was used to examine the microstructure. The main crystalline phases formed are related to the expected with the equilibrium phase diagram of the ZrO₂–CaO–Al₂O₃ system. Stabilized c-ZrO₂ is formed with the composition of Ca_0.15Zr_0.85O_1.85. The sintering of the mixtures leads to porous composites materials. Textural properties were analyzed considering the initial composition and the present crystalline phases.     

Electrical properties and microstructural evolution of ZrO2–Al2O3–TiN nanocomposites prepared by spark plasma sintering

Electroconductive ZrO₂–Al₂O₃–25 vol% TiN ceramic nanocomposites were prepared by spark plasma sintering at 1200 °C for 3 min. The electrical resistivity of the composites decreased from 4.5 × 10^?4 Ω m to 3 × 10^?5 Ω m as the Al₂O₃ content in the ZrO₂–Al₂O₃ matrix increased from 0 to 100 vol%. SEM images graphically presented the microstructural evolution of the composites and a geometrical percolation model was applied to investigate the relationship between the electrical property and the microstructure. The results indicated that the addition of Al₂O₃ to ZrO₂–TiN improved the electrical conductivity of the material by tailoring the structure from “nano–nano” type for ZrO₂–TiN to “micro–nano” type for ZrO₂–Al₂O₃–TiN.     

Enhanced production of benzyl alcohol in the gas phase continuous hydrogenation of benzaldehyde over Au/Al2O3

Exclusive hydrogenation of benzaldehyde to benzyl alcohol in gas phase continuous operation (393–413 K, 1 atm) was achieved over Au/Al₂O₃, Au/TiO₂ and Au/ZrO₂. Synthesis of Au/Al₂O₃ by deposition–precipitation generated a narrower distribution (2–8 nm) of smaller (mean = 4.3 nm) Au particles relative to impregnation (1–21 nm, mean = 7.9 nm) with increased H₂ uptake under reaction conditions and higher benzaldehyde turnover. Switching reactant carrier from ethanol to water resulted in a significant enhancement of selective hydrogenation rate over Au/Al₂O₃ with 100% benzyl alcohol yield, attributed to increased available reactive hydrogen. This response extends to reaction over Au/TiO₂ and Au/ZrO₂.     

Superplastic deformation of directionally solidified nanofibrillar Al2O3–Y3Al5O12–ZrO2 eutectics

Nanofibrillar Al₂O₃–Y₃Al₅O₁₂–ZrO₂ eutectic rods were manufactured by directional solidification from the melt at high growth rates in an inert atmosphere using the laser-heated floating zone method. Under conditions of cooperative growth, the ternary eutectic presented a homogeneous microstructure, formed by bundles of single-crystal c-oriented Al₂O₃ and Y₃Al₅O₁₂ (YAG) whiskers of ≈100 nm in width with smaller Y₂O₃-doped ZrO₂ (YSZ) whiskers between them. Owing to the anisotropic fibrillar microstructure, Al₂O₃–YAG–YSZ ternary eutectics present high strength and toughness at ambient temperature while they exhibit superplastic behavior at 1600 K and above. Careful examination of the deformed samples by transmission electron microscopy did not show any evidence of dislocation activity and superplastic deformation was attributed to mass-transport by diffusion within the nanometric domains. This combination of high strength and toughness at ambient temperature together with the ability to support large deformations without failure above 1600 K is unique and shows a large potential to develop new structural materials for very high temperature structural applications.     

Calcium Cl/OH-apatite,Cl/OH-apatite/Al2O3 and Ca3(PO4)2 fibre nonwovens: Potential ceramic components for osteosynthesis

Polycrystalline calcium phosphate ((Cl/OH)Ap = Ca₅(PO₄)₃(OH/Cl); TCP = Ca₃(PO₄)₂) fibres were prepared from aqueous solutions of calcium chloride and phosphoric acid using poly(ethylene oxide) (PEO) as spinning aid. Generation of nonwoven materials was accomplished via rotary jet spinning. Polycrystalline (Cl/OH)Ap fibres 10–25 μm in diameter were obtained with 37% ceramic yield by pyrolysis of the green fibres followed by sintering at 1150 °C in air. X-ray diffraction (XRD) analysis provided evidence for apatite formation starting at 650 °C while (Cl/OH)Ap ceramic fibres were obtained at 1100 °C via transformation through intermediate dicalcium dichloride hydrogen phosphate (Ca₂Cl₂(HPO₄)) and calcium pyrophosphate (Ca₂P₂O₇) phases. A glass-forming Al-based additive was applied to enhance the mechanical properties of the Cl/OH)Ap ceramic fibres and indeed resulted in the formation of (Cl/OH)Ap/Al₂O₃ fibres with improved mechanical stability. Finally, TCP, (Cl/OH)Ap and (Cl/OH)Ap/Al₂O₃ fibres were subjected to seeding with mesenchymal stem cells. Negligible cytotoxicity is observed.     

Effect of solidification path on the microstructure of Al2O3–Y2O3–ZrO2 ternary oxide eutectic ceramic system

The solidification path of the Al₂O₃–Y₂O₃–ZrO₂ ternary oxide eutectic composite ceramic is determined by a high temperature DTA and laser floating zone (LFZ) directional solidification method to investigate the effect of solidification path on the microstructure of the ternary oxide. The DTA and microstructure analyses show that the YAG or Al₂O₃ tends to form as primary phase under the unconstrained solidification conditions, and then the system enters ternary eutectic solidification during cooling from 1950 °C at rate of 20 °C/min. The as-solidified composite ceramic shows a divorced irregular eutectic structure consisting of Al₂O₃, YAG and ZrO₂ phases with a random distribution. The primary phases are however completely restrained at the directional solidification conditions with high temperature gradient, and the ternary composite by LFZ presents well coupled eutectic growth with ultra-fine microstructure and directional array. Furthermore, the eutectic transformation and growth mechanism of the composite ceramic under different solidification conditions are discussed.     

Fabrication of pressureless sintered dense β-SiAlON via a reaction-bonding route with ZrO2 addition

A reaction-bonding and post-sintering process was applied to fabricate pressureless sintered β-Si_6?ZAl_ZO_ZN_8?Z (Z = 1–3) ceramics with monoclinic ZrO₂ added to the starting powder. Samples with ZrO₂ showed enhanced nitridation and achieved near theoretical density following post-sintering, although this could not be achieved in the samples produced without ZrO₂. Thus the ZrO₂ is effective in both enhancing the nitridation of Si and as a sintering additive for densification of β-SiAlON. Part of the added monoclinic ZrO₂ was transformed to tetragonal ZrO₂, and the ZrN phase was also formed due to reaction with nitrogen during the reaction-bonding process. After the post-sintering process, the ZrN phase remained only in the Z = 3 composition. In the other compositions the ZrN reacted with SiO₂ to form both tetragonal and monoclinic ZrO₂ phases. These differences are explained in terms of the increasing densification and grain growth for Al₂O₃ rich compositions and the ZrN being trapped inside such grains in the case of the Z = 3 sample.     

Lamellar-interpenetrated Al−Si−Mg/Al2O3−ZrO2 composites prepared by freeze casting and pressureless infiltration

Using freeze casting and pressureless infiltration methods, we prepared lamellar Al−Si−Mg/Al₂O₃−ZrO₂ composites with initial ceramic loading of 30 vol% and different Al₂O₃:ZrO₂ weight ratios (Al₂O₃:ZrO₂=1:9, 3:7, 5:5, 7:3 and 9:1). The resultant composites inherited the lamellar structure of the Al₂O₃−ZrO₂ scaffolds, and the thickness of both metal and ceramic layers showed a trend of first increase and then decrease with increasing Al₂O₃ content. During pressureless infiltration, multiple chemical reactions took place between ZrO₂ and the Al−12Si−10Mg alloy and the main reaction products were (Al_1−m, Si_m)₃Zr, Al₂O₃ and ZrSi₂ phases. The degree of the reaction depended on the ZrO₂ content in the ceramic composition. In general, the compressive strength of the composites decreased with increasing Al₂O₃ content, but three-point bending strength showed a first decrease and then increase. When Al₂O₃:ZrO₂=1:9, the compressive and bending strength of the composites reached about 997±60 MPa and 426±10 MPa, respectively. A simple model was proposed to illustrate the fracture mode and toughening mechanism of the composites.     

Preparation and characterization of Al2O3–25 mol% ZrO2 composites

Al₂O₃–ZrO₂ (AZ_x), with 25 mol% ZrO₂ content, was prepared using the co-precipitation method. Synthesized powders were characterized by thermal reaction using a differential thermal analysis technique (TG–DTA) and were investigated by phase formation using X-ray diffraction. It indicated that the reaction occurred at 850 °C; cubic (c)-ZrO₂ phase and Al₂O₃ were obtained. By increasing temperature to 1100 °C, tetragonal (t)-ZrO₂ phase was detected. The Al₂O₃–25 mol% ZrO₂ was sintered for 2 h in the temperature range of between 1300 and 1600 °C. The majority phases of ceramics were m-ZrO₂ and α-Al₂O₃, although a t-ZrO₂ phase also appeared as a minor phase and decreased with higher temperature. Moreover, morphology and particle size evolution have been determined via the SEM technique. SEM showed that the particles of powder are agglomerated and basically irregular in shape. An SEM micrograph of ceramics exhibits uniform microstructure without abnormal grain growth.