Uniformity of Al2O3-ZrO2 Composites by Colloidal Filtration

Dispersion states of aqueous composite Al₂O₃/ZrO₂ colloidal suspensions were studied by measuring particle size distribution as a function of pH. Mutual dispersion was achieved at pH values of 2.0 to 3.5. Consolidated composites formed by colloidal filtration reflected the uniformity of the colloidal state. The mean flexural strength (896 MPa) of the sintered compacts was 1.6 times that of bodies consolidated by isostatic pressing .     

Fabrication of a Continuously Oriented Porous Al2O3 Body and Its In Vitro Study

Continuously oriented porous Al₂O₃ bodies were fabricated by a multi-pass extrusion process using C powders and ethylene vinyl acetate as an agent for pore forming and as a binder, respectively. The main pore size can be easily controlled by increasing the number of extrusion passes. The edges of the pore frame showed a rough surface having many fine pores about 0.2–1 μm in size. In the continuously porous Al₂O₃ bodies having 150 μm pore size, the values of the relative density and bending strength were about 63% and 90 MPa, respectively. These values were higher than those of an Al₂O₃ porous body made by a common process. From the in vitro study using human osteoblast-like MG-63 cells, it was confirmed that the cells grew well and adhered to the top surface and inside pores, as well as the outside wall of the continuously porous Al₂O₃ body. Without the directionality, the cells showed some spindle-shaped, three-dimensional, and network-type structures.     

Compaction and Pressureless Sintering of Zirconia Nanoparticles

Four nanometer-sized zirconia powders stabilized by 3 mol% Y₂O₃ were used for the preparation of dense bulk ceramics. Ceramic green bodies were prepared by cold isostatic pressing at pressures of 300–1000 MPa. The size of the pores in ceramic green bodies and their evolution during sintering were correlated with the characteristics of individual nanopowders and with the sintering behavior of powder compacts. Only homogeneous green bodies with pores of <10 nm could be sintered into dense bodies (>99% t.d.) at a sufficiently low temperature to keep the grain sizes in the range <100 nm. Powders with uniform particles 10 nm in size yielded green bodies of required microstructure. These nanoparticle compacts were sintered without pressure to give bodies (diameter 20 mm, thickness 4 mm) with a relative density higher than 99% and a grain size of about 85 nm (as determined by the linear intercept method).     

Preparation and Properties of Porous α-Al2O3 Membrane Supports

Strong and permeable macro-porous α-Al₂O₃ membrane supports are made by colloidal filtration of 20 vol% dispersions of α-Al₂O₃ with an average particle size of 600 nm. Intact compacts with very good surface quality were obtained at an optimum pH of 9.5 and dosage of 0.2 wt% ammonium aurintricarboxylate (Aluminon), based on dry alumina. The colloidal stability of the aluminon-stabilized slurries is confirmed by ξ potential measurements. Slight sintering of dense-packed α-Al₂O₃ compacts was found to result in >67% packing density and a bimodal pore-size distribution as derived from shrinkage behavior and gas adsorption studies. Non-stationary single gas permeation measurements showed improved gas permeability, compared with α-Al₂O₃ compacts prepared using powder with a smaller particle size (300 nm). The strength of the disk-shaped alumina compacts within the porosity range of 30%–20% increased from 100 to 300 MPa with a standard deviation of 20 and 50 MPa, respectively.     

Relationship Between Microstructures and Material Properties of Novel Fibrous Al2O3–(m-ZrO2)/t-ZrO2 Composites

Novel fibrous Al₂O₃–(m-ZrO₂)/t-ZrO₂ (m, monoclinic; t, tetragonal) composites having a core/shell structure were fabricated by multi-extrusion, and their microstructures and material properties were investigated depending on the number of extrusions. The composites acquired a homogeneously fine fibrous structure as the number of extrusions increased. The bending strength and fracture toughness increased remarkably as the number of extrusions increased. In the fracture surface of the second passed composite, an Al₂O₃–(m-ZrO₂) core region appeared, flat type, although some local regions existed with an intergranular fracture. However, the fracture mode of the t-ZrO₂ region was of intergranular type having a sharp and rough surface. In the composite made by the fifth passed extrusion, the fracture strength and toughness values were high at about 665 MPa and 9.6 MPa·m^1/2, respectively. The main fracture mode was a typical intergranular mode having a rough fracture surface, and the main multi-toughening was because of mechanisms such as crack bridging, microcracking, and phase transformation.     

Strength-Toughness Relations in Sintered and Isostatically Hot-Pressed ZrO2-Toughened Al2O3

The fracture toughness of fine-grained undoped ZrO₂-toughened Al₂O₃ (ZTA) was essentially unchanged by postsintering hot isostatic pressing and increased monotonically with ZrO₂ additions up to 25 wt%. The strength of ZTA with 5 to 15 wt% tetragonal ZrO₂, which depended monotonically on the amount of ZrO₂ present before hot isostatic pressing, was increased by pressing but became almost constant between 5 and 15 wt% ZrO₂ addition. The strength appeared to be controlled by pores before pressing and by surface flaws after pressing; the size of flaws after pressing increased with ZrO₂ content. The strength of ZTA containing mostly monoclinic ZrO₂ (20 to 25 wt%) remained almost constant despite the noticeable density increase upon hot isostatic pressing because the strength was controlled by preexisting microcracks whose extent did not change on postsintering pressing. These strength-toughness relations in sintered and isostatically hot-pressed ZTA are explained on the basis of R -curve behavior. The importance of the contribution of microcracks to the toughness of ZTA is emphasized.     

Electroconductive Al2O3–NbN Composites

Electroconductive Al₂O₃–NbN ceramic composites were prepared by hot pressing. Dense sintered bodies of ball-milled Al₂O₃–NbN composite powders were obtained at 1550°C and 30 MPa for 1 h under a nitrogen atmosphere. The bending strength and fracture toughness of the composites were enhanced by incorporating niobium nitride (NbN) particles into the Al₂O₃ matrix. The electrical resistivity of the composites decreased with increasing amount of NbN phase. For a 25 vol% NbN–Al₂O₃ composite, the values of bending strength, fracture toughness, Vickers hardness, and electrical resistivity were 444.2 MPa, 4.59 MPa·m^1/2, 16.62 GPa, and 1.72 × 10⁻²Ω·cm, respectively, making the composite suitable for electrical discharge machining.     

Field-Assisted Densification of Superhard B6O Materials with Y2O3/Al2O3 Addition

B₆O is a possible candidate of superhard materials with a hardness of 45 GPa measured on single crystals. Up to now, densification of these materials was only possible at high pressure. However, recently it was found that Al₂O₃ can be utilized as an effective sintering additive, similar to the addition of Y₂O₃/Al₂O₃ that was used in this work. The densification behavior of the material as a function of applied pressure, its microstructure evolution, and the resulting mechanical properties were investigated. A strong dependence of the densification with increasing pressure was found. The material revealed characteristic triple junctions filled with amorphous residue composed of B₂O₃, Al₂O₃, and Y₂O₃, while no amorphous grain-boundary films were observed along internal interfaces. Mechanical testing revealed on average a hardness of 33 GPa, a fracture toughness of 4 MPa·m^1/2, and a strength value of 520 MPa.     

Reinforcement of Hydroxyapatite Bioceramic by Addition of Ni3Al and Al2O3

The effects of Ni₃Al and Al₂O₃ additions on the mechanical properties of hydroxyapatite (HAp) were investigated. The addition of Ni₃Al particles increased the strength as well as the fracture toughness of HAp. However, the improvements in the properties were limited because of the formation of microcracks around the metal particles. The microcracks were formed because of the large difference in the coefficients of thermal expansion between HAp and Ni₃Al, and because of the relatively large size of Ni₃Al particles (∼20 µm). The addition of submicrometer Al₂O₃ powder was also effective in increasing the mechanical properties. The flexural strength and the fracture toughness were increased from about 100 MPa and 0.7 MPam^1/2, respectively, to 200 MPa and 1.5 MPam^1/2 by the addition of 20 vol% Al₂O₃. When Ni₃Al and Al₂O₃ were added together, the fracture toughness was further increased to 2.3 MPam^1/2. This increase in the fracture toughness was attributed to the synergistic effect of matrix strengthening and crack interactions with the metal particles.     

Translucent Al2O3/LaAl11O18 Composite

A translucent alumina composite containing 1 vol% LaAl₁₁O₁₈, prepared by the hot isostatic pressing (HIP) method, displays both high translucency and high fracture toughness. Its total forward transmission at 600 nm is 75% (thickness 1 mm), and its bending strength and fracture toughness are estimated to be 574±15 MPa and 5.9±0.46 MPa·m^0.5, respectively. Its high translucency is due to the similarity of refractive index between the additive phase (LaAl₁₁O₁₈) and the matrix (alumina).     

Strength and Fracture Toughness of Isostatically Hot-Pressed Composites of Al2O3 and Y2O3-Partially-Stabilized ZrO2

Composites of Al₂O₃ and Y₂O₃ partially-stabilized ZrO₂ were isostatically hot-pressed using submicrometer powders as the starting material. The addition of Al₂O₃ resulted in a large increase in bending strength. The average bending strength for a composite containing 20 wt% Al₂O₃ was 2400 MPa, and its fracture toughness was 17 MN·w^−3/2     

Densification and Grain Growth of Al2O3 Nanoceramics During Pressureless Sintering

α - Al₂O₃ nanopowders with mean particle sizes of 10, 15, 48, and 80 nm synthesized by the doped α-Al₂O₃ seed polyacrylamide gel method were used to sinter bulk Al₂O₃ nanoceramics. The relative density of the Al₂O₃ nanoceramics increases with increasing compaction pressure on the green compacts and decreasing mean particle size of the starting α-Al₂O₃ nanopowders. The densification and fast grain growth of the Al₂O₃ nanoceramics occur in different temperature ranges. The Al₂O₃ nanoceramics with an average grain size of 70 nm and a relative density of 95% were obtained by a two-step sintering method. The densification and the suppression of the grain growth are achieved by exploiting the difference in kinetics between grain-boundary diffusion and grain-boundary migration. The densification was realized by the slower grain-boundary diffusion without promoting grain growth in second-step sintering.     

High-Strength and High-Fracture-Toughness Ceramics in the Al2O3/LaAl11O18 Systems

Control of microstructure in the Al₂O₃/LaAl₁₁O₁₈ system was performed. Elongated alumina grains were formed by doping with small addition of silica, and 20 vol% lanthana- luminate was formed in situ by the reaction of LaAlO₃- A1₂O₃ in an alumina matrix. Strengths of over 600 MPa and a high fracture toughness (6 MPa.m^1/2) were achieved in the material with both elongated A1₂O₃ grains and LaAl₁₁O₁₈ platelets. Generally antagonistic properties such as strength and fracture toughness have been made compatible in the same ceramic system.     

High-Temperature Strength and Fracture Toughness of Y2O3-Partially-Stabilized ZrO2/Al2O3 Composites

The temperature dependence of bending strength, fracture toughness, and Young's modulus of composite materials fabricated in the ZrO₂ (Y₂O₃)-Al₂O₃ system were examined. The addition of A1203 enhanced the high-temperature strength. Isostatically hot-pressed, 60 wt% ZrO₂ (2 mol% Y₂O₃)/40 wt% Al₂O₃ exhibited an extremely high strength, 1000 MPa, at 1000°C.     

Fracture Strength–Fracture Resistance Response and Damage Resistance of Sintered Al2O3–ZrO2 (12 mol% CeO2) Composites

The fracture strengths of sintered Al₂O₃ containing 20 and 40 vol% ZrO₂(12 mol% CeO₂)—zirconia-toughened alumina (ZTA)—composites along with the fracture resistance can be increased (e.g., to ∼900 MPa and >12 Mpa·m^1/2, respectively), by increasing the mean grain size of the t -ZrO₂ (and the Al₂O₃) from ∼0.5 μm to ∼3 μm. At these lower t -ZrO₂ contents, the fracture strength-fracture resistance curves show a continuous rise as opposed to the strength maxima observed in polycrystalline t -ZrO₂(12 mol% CeO₂), CeTZP, and ZrO₂(12 mol% CeO₂) ceramics containing ≤20 vol% Al₂O₃. The toughened composites also exhibit excellent damage resistance with fracture strengths of 500 MPa retained with surfaces containing ∼150- N Vickers indentations which produce cracks of ∼160-μm radius. Greater damage resistance correlates with an increase in the apparent R -curve response of these composites.     

Transformation Plasticity and Toughening in CeO2-Partially-Stabilized Zirconia–Alumina (Ce-TZP/Al2O3) Composites Doped with MnO

Microstructure, phase stability, and mechanical properties of CeO₂-partially-stabilized zirconia (12 mol% Ce-TZP) containing 10 wt% Al₂O₃ and 1.5 wt% MnO were studied in relation to the base Ce-TZP and the Ce-TZP/Al₂O₃ composite without MnO. The MnO reacted with both CeO₂ and Al₂O₃ to form a new phase of approximate composition CeMnAl₁₁O₁₉. The reacted phase had a magnetoplumbite structure and formed elongated, needlelike crystals. The MnO-doped Ce-TZP/Al₂O₃ composites sintered at an optimum temperature of 1550°C exhibited high strength (650 MPa in four-point bending) and rising crack-growth-resistance behavior, with fracture toughness increasing from 7.6 to 10.3 MPa.In¹² in compact tension tests. These improved mechanical properties were associated with relatively high tetragonal-to-monoclinic transformation temperature ( M _s=−42°C) at small grain size (2.5 μm), significant transformation plasticity in mechanical tests (bending, uniaxial tension, and uniaxial compression) and transformation zones at crack tips in compact tension specimens. The transformation yield stress, zone size, and fracture toughness were sensitive to the sintering temperature varied in the range 1500° to 1600°C. Analysis of the transformation zones using Raman microprobe spectroscopy and calculation of zone shielding for the observed zones indicated that a large fraction of the fracture toughness (∼70%) was derived from transformation toughening.     

Formation, Characterization, and Hot Isostatic Pressing of Cr2O3-Doped ZrO2 (0,3 mol% Y2O3) Prepared by Hydrazine Method

In the ZrO₂-Cr₂O₃ system, metastable t -ZrO₂ solid solutions containing up to 11 mol% Cr₂O₃ crystallize at low temperatures from amorphous materials prepared by the hydrazine method. The lattice parameter c decreases linearly from 0.5149 to 0.5077 nm with increased Cr₂O₃ content, whereas the lattice parameter a is a constant value ( a = 0.5077 nm) regardless of the starting composition. At higher temperatures, transformation (decomposition) of the solid solutions proceeds in the following way: t (ss)→ t (ss) + m + Cr₂O₃→ m + Cr₂O₃. Above 11 mol% Cr₂O₃ addition, c-ZrO₂ phases are formed in the presence of Cr₂O₃. The t -ZrO₂ solid solution powders have been characterized for particle size, shape, and surface area. They consist of very fine particles (15–30 nm) showing thin platelike morphology. Dense ZrO₂(3Y)-Cr₂O₃ composite ceramics (∼99.7% of theoretical) with an average grain size of 0.3 μm have been fabricated by hot isostatic pressing for 2 h at 1400°C and 196 MPa. Their fracture toughness increases with increased Cr₂O₃ content. The highest K _Ic value of 9.5 MPa·;m^1/2 is achieved in the composite ceramics containing 10 mol% Cr₂O₃.     

High Electrical Conductivity and High Fracture Strength of Sc2O3-Doped Zirconia Ceramics with Submicrometer Grains

The microstructure, crystal phase, electrical conductivity, and mechanical strength of less than 7-mol%-Sc₂O₃-doped zirconia ceramics fabricated by comparatively low-temperature sintering at 1200–1300°C for 1 h were investigated. Zirconia ceramics having a uniform microstructure (grain size < 0.5 μm) stabilized with 6 mol% Sc₂O₃ showed high electrical conductivity (0.15 S/cm at 1000°C) and high fracture strength (660 MPa). With the increase of Sc₂O₃ content from 3.5 to 7 mol%, the grain size, fracture strength, and electrical conductivity at 1000°C changed from 0.2 to 0.5 μm, 970 to 440 MPa, and 0.07 to >0.2 S/cm, respectively. Sc₂O₃-doped zirconia polycrystals with high fracture strength and high electrical conductivity are promising candidates for the electrolyte material of solid oxide fuel cells.     

Mechanical properties of toughened ZrO2-Y2O3 Ceramics

Tetragonal zirconia polycrystals were produced from high-purity powders containing 1.5 to 5.0 mol% Y₂O₃ by cold isostatic pressing and sintering, hot-pressing, and hot isostatic pressing. The mechanical properties and microstructures of these resulting materials were examined, with emphasis on the relation between strength and fracture toughness.     

Room-Temperature Strength and Fracture of ZrO2-Y2O3 Single Crystals

Strength and fracture toughness results are presented for ZrO₂ single crystals stabilized with Y₂O₃. The crystals (2 cm in diameter by 5 cm long) were prepared by skull melting. The partially stabilized compositions with 4 to 6 wt% Y₂O₃ showed a dramatic improvement in mechanical properties over the fully stabilized samples containing 20 wt% Y₂O₃, i.e. a strength exceeding 1000 MPa and a fracture toughness of 8 Mpa,.m ^1/2 were achieved compared to 200 MPa and 2 Mpa.m^1/2, respectively, for fully stabilized ZrO₂ single crystals.