Postsintering Hot Isostatic Pressing of Ceria-Doped Tetragonal Zirconia/Alumina Composites in an Argon–Oxygen Gas Atmosphere

Ceria-doped tetragonal zirconia (Ce-TZP)/alumina (Al₂O₃) composites were fabricated by sintering at 1450° to 1600°C in air, followed by hot isostatic pressing (postsintering hot isostatic pressing) at 1450°C and 100 MPa in an 80 vol% Ar–20 vol% O₂ gas atmosphere. Dispersion of Al₂O₃ particles into Ce-TZP was useful in increasing the relative density and suppressing the grain growth of Ce-TZP before hot isostatic pressing, but improvement of the fracture strength and fracture toughness was limited. Postsintering hot isostatic pressing was useful to densify Ce-TZP/Al₂O₃ composites without grain growth and to improve the fracture strength and thermal shock resistance.     

Fracture Behavior of SiC-Whisker-Reinforced Barium Aluminosilicate Glass-Ceramic Matrix Composites

Barium aluminosilicate (BAS) glass-ceramic composites reinforced with various volume percents (0, 10, 20, 30, 40 vol%) of SiC whiskers were fabricated by hot pressing. The microstructure, the whisker/matrix interface structure, the phase constitution, and the mechanical properties of the composites were systematically studied by means of SEM, TEM, and XRD techniques as well as by indentation crack microfracture and single-edge-notched-beam bend testing. It was demonstrated that the incorporation of SiC whiskers could significantly increase the flexural strength and fracture toughness of BAS glass-ceramic matrices. The addition of active Al₂O₃ to the BAS matrix reduced the amount of SiO₂ in the matrix, forming needlelike mullite, which further improved the mechanical properties.     

Fabrication and Characterization of ZrB2-Based Ceramic Using Synthesized ZrB2–LaB6 Powder

ZrB₂–LaB₆ powder was obtained by reactive synthesis using ZrO₂, La₂O₃, B₄C, and carbon powders. Then ZrB₂–20 vol% SiC–10 vol% LaB₆ (ZSL) ceramics were prepared from commercially available SiC and the synthesized ZrB₂–LaB₆ powder via hot pressing at 2000°C. The phase composition, microstructure, and mechanical properties were characterized. Results showed that both LaB₆ and SiC were uniformly distributed in the ZrB₂ matrix. The hardness and bending strength of ZSL were 17.06±0.52 GPa and 505.8±17.9 MPa, respectively. Fracture toughness was 5.7±0.39 MPa·m^1/2, which is significantly higher than that reported for ZrB₂–20 vol% SiC ceramics, due to enhanced crack deflection and crack bridging near SiC particles.     

High-Strength Zirconium Diboride-Based Ceramics

Zirconium diboride (ZrB₂) and ZrB₂ ceramics containing 10, 20, and 30 vol% SiC particulates were prepared from commercially available powders by hot pressing. Four-point bend strength, fracture toughness, elastic modulus, and hardness were measured. Modulus and hardness did not vary significantly with SiC content. In contrast, strength and toughness increased as SiC content increased. Strength increased from 565 MPa for ZrB₂ to >1000 MPa for samples containing 20 or 30 vol% SiC. The increase in strength was attributed to a decrease in grain size and the presence of WC.     

Homogeneous Fabrication of Al2O3–ZrO2–SiC Whisker Composite by Surface-Induced Coating

Al₂O₃–ZrO₂–SiC whisker composites were prepared by surface-induced coating of the precursor for the ZrO₂ phase on the kinetically stable colloid particles of Al₂O₃ and SiC whisker. The fabricated composites were characterized by a uniform spatial distribution of ZrO₂ and SiC whisker phases throughout the Al₂O₃ matrix. The fracture toughness values of the Al₂O₃–15 vol% ZrO₂–20 vol% SiC whisker composites (∼12 MPa.m^1/2) are substantially greater than those of comparable Al₂O₃–SiC whisker composites, indicating that both the toughening resulting from the process zone mechanism and that caused by the reinforced SiC whiskers work simultaneously in hot-pressed composites.     

Al2O3–Ni Composites with High Strength and Fracture Toughness

Al₂O₃–Ni composites were prepared by the reactive hot pressing of Al and NiO. The composites had a two-phase, interpenetrating microstructure and contained ∼35 vol% Ni. They exhibited an impressively high combination of strength and toughness at room temperature; the four-point bending strength was in excess of 600 MPa with a fracture toughness of more than 12 MPa·m^1/2. Examination of fracture surfaces showed that Ni ligaments underwent ductile deformation during fracture. SEM analysis revealed knife-edged Ni ligaments with a limited amount of debonding around their periphery (i.e., at the Ni–Al₂O₃ interface), indicating a strong Ni–Al₂O₃ bond.     

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.     

Reactive Hot Pressing of Alumina-Silicon Carbide Nanocomposites

A dense alumina-silicon carbide (Al₂O₃–SiC) nanocomposite was synthesized in situ from the reaction of mullite, aluminum, and carbon by reactive hot pressing (RHP). Transmission electron microscopy investigation showed that in situ -formed, nanometer-sized SiC particles were mainly entrapped in the matrix grains, whereas submicrometer-sized particles were located at the grain boundaries or triple points of the Al₂O₃. In addition, no amorphous phase was observed at the interfaces of the Al₂O₃ and SiC grains, which indicated strong direct bonding. Fracture-surface analysis by scanning electron microscopy revealed an intrafracture mode. The bending strength of the nanocomposite RHP-treated at 1800°C was 795 ± 160 MPa, and the fracture toughness, measured by the indentation method, was 3.1 MPa·m^1/2.     

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).     

Silicon Carbide Whisker/Alumina Matrix Composites: Effect of Whisker Surface Treatment on Fracture Toughness

The fracture toughness of a 30 vol% SiC whisker/Al₂O₃ matrix composite was evaluated as a function of whisker surface chemistry. Two types of SiC whiskers (Silar-SC-9 and Tateho-SCW-1-S) were investigated. Modification of the whisker surface chemistry was achieved by subjecting the whiskers to thermal treatments under controlled atmospheres. Whisker surface chemistry, as determined by X-ray photoelectron spectroscopy, was correlated to the fracture toughness of the composites.     

Fracture Toughness of Al2O3-Particle-Dispersed Y2O3-Partially Stabilized Zirconia

The fracture toughness of 3 mol% Y₂O₃-ZrO₂ (3Y-PSZ) composites containing 10–30 vol% Al₂O₃ with different particle sizes was investigated. It was found that Al₂O₃ dispersion of up to 30 vol% increased the fracture toughness by 17% to 30%, and the toughness increase was more remarkable in the composite dispersed with Al₂O₃ particles of larger sizes. By combining the effects of the dispersion toughening and phase transformation toughening, the toughness change in the present materials was theoretically predicted, which was in good agreement with the experimental data.     

A Strong and Damage-Tolerant Oxide Laminate

A novel laminar oxide composite was developed. This oxide laminate, which was fabricated by hot pressing, consisted of three types of layers, which were stacked in a repeating sequence of YPO4, yttria-stabilized ZrO₂, 30 vol% yttria-stabilized ZrO₂-70 vol% Al₂O₃, and yttria-stabilized ZrO₂. The behavior of the oxide laminate was evaluated by four-point flexural testing and the indentation technique. The flexural strength from one test was 358 MPa, and the load-displacement curve of this test displayed a graceful failure. Pronounced interfacial delamination contributed to a high work of fracture and damage tolerance. These properties have rarely been observed in oxide composites and are comparable to those of non-oxide composites, such as SiC/graphite, SiC/BN, and Si₃N₄/BN laminates.     

Mechanical Behavior of Alumina–Silicon Carbide „Nanocomposites”

The fracture behavior of Al₂O₃ containing 5 vol% 0.15μm SiC particles was investigated using indentation techniques. A significant increase in strength was achieved by the addition of SiC particles to the base Al₂O₃. Specifically, the strength increased from 560 MPa for Al₂O₃ to 760 MPa for the composite samples (average values for unindented hotpressed bars tested in four-point bending). After annealing for 2 h at 1300°C, the average strength of the composite samples increased to about 1000 MPa. Toughness was estimated using indentation-strength data. While there was a slight increase in toughness, the increase was not sufficient to account for the increase in the unindented strength on SiC particle addition. It is suggested that the observed strengthening and apparent toughening were due to a machining-induced compressive surface stress.     

Effects of Zirconium Doping on Grain-Boundary Bonding in Alumina-Silicon Carbide Composites

In this work, 800 ppm of Zr⁴⁺ dopants were added to Al₂O₃-5 vol% SiC particle composite. Zr⁴⁺ doping led to a weak Al₂O₃ grain-boundary bonding so that the fracture mode changed from transgranular in undoped composite to intergranular in Zr⁴⁺-doped composite. The fracture mode change increased the fracture toughness of the composite. Transmission electron microscopy and energy-dispersive spectroscopy examinations revealed that the weak grain-boundary bonding in the doped composite was caused by the segregation of Zr⁴⁺ and Si⁴⁺ ions at the Al₂O₃ grain boundary.     

Reactive Hot Pressing of SiC/MoSi2 Nanocomposites

Dense SiC/MoSi₂ nanocomposites were fabricated by reactive hot pressing the mixed powders of Mo, Si, and nano-SiC particles coated homogeneously on the surface of Si powder by polymer processing. Phase composition and microstructure were determined by methods of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and energy-dispersive spectrometry. The nanocomposites obtained consisted of MoSi₂, β-SiC, less Mo₅Si₃, and SiO₂. A uniform dispersion of nano-SiC particles was obtained in the MoSi₂ matrix. The relative densities of the monolithic material and nanocomposite were above 98%. The room-temperature flexural strength of 15 vol% SiC/MoSi₂ nanocomposite was 610 MPa, which increased 141% compared with that of the monolithic MoSi₂. The fracture toughness of the nanocomposite exceeded that of pure MoSi₂, and the 1200°C yield strength measured for the nanocomposite reached 720 MPa.     

Reaction Bonding and Mechanical Properties of Mullite/Silicon Carbide Composites

Based on the RBAO technology, low-shrinkage mullite/SiC/ Al₂O₃/ZrO₂ composites were fabricated. A powder mixture of 40 vol% Al, 30 vol% A1₂O₃ and 30 vol% SiC was attrition milled in acetone with TZP balls which introduced a substantial ZrO₂ wear debris into the mixture. The precursor powder was isopressed at 300–900 MPa and heattreated in air by two different cycles resulting in various phase ratios in the final products. During heating, Al oxidizes to Al₂O₃ completely, while SiC oxidizes to SiO₂ only on its surface. Fast densification (at >1300°C) and mullite formation (at 1400°C) prevent further oxidation of the SiC particles. Because of the volume expansion associated with the oxidation of Al (28%), SiC (108%), and the mullitization (4.2%), sintering shrinkage is effectively compensated. The reaction-bonded composites exhibit low linear shrinkages and high strengths: shrinkages of 7.2%, 4.8%, and 3%, and strengths of 610, 580, and 490 MPa, corresponding to compaction pressure of 300, 600, and 900 MPa, respectively, were achieved in samples containing 49–55 vol% mullite. HIPing improved significantly the mechanical properties: a fracture strength of 490 MPa and a toughness of 4.1 MPa^.m^1/2 increased to 890 MPa and 6 MPa^.m^1/2, respectively.     

Evidence for Bulk Residual Stress Strengthening in Al2O3/SiC Nanocomposites

The fracture behavior of Al₂O₃/SiC nanocomposites has been studied as a function of the SiC volume fraction and compared to that of the pure Al₂O₃ matrix. A pronounced strengthening effect was only observed for materials with low SiC content (i.e., ≤10 vol%) although no evidence of concurrent toughening was found. Assessment of near-tip crack opening displacement (COD) could not experimentally substantiate significant occurrence of an elastic crack-bridging mechanism, in contrast with a recently proposed literature model. Quantitative fractography analysis indicated that transgranular crack propagation in Al₂O₃/SiC nanocomposites depends on the location of the SiC dispersoids within the matrix texture; the higher the fraction of transgranularly located dispersoids, the more transgranular the fracture mode. Experimental evidence of remarkably high residual stresses arising from thermal dilatation mismatch (upon cooling) between Al₂O₃ and SiC phases were obtained by fluorescence and Raman spectroscopy. A strengthening mechanism is invoked which merely arises from residual stress through strengthening of Al₂O₃ grain boundaries.     

Mechanical Properties of Al2O3-NiAl Composites

The mechanical properties of the Al₂O₃-NiAl system are investigated in the present study. Specimens containing 0 to 100 vol% NiAl in Al₂O₃ were prepared by hot pressing. Both the strength and toughness of the Al₂O₃-NiAl composites are higher than the values predicted by the rule of mixtures. The grain growth of Al₂O₃ and NiAl in the composites is constrained by each component. The increase in strength is thus partly attributed to microstructural refinement. The toughness enhancement is contributed by a combination of crack deflection and crack bridging.     

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.     

Preparation and Microstructure of Multi-Wall Carbon Nanotubes-Toughened Al2O3 Composite

With multi-wall carbon nanotubes (MWNTs) as reinforcement, a 12 vol% MWNTs/alumina (Al₂O₃) ceramic composite was obtained by hot pressing. A fracture toughness of 5.55±0.26 MPa·m^1/2, 1.8 times that of pure Al₂O₃ ceramics, was achieved. Experimental results showed that the enveloping of carbon nanotubes (CNTs) with sodium dodecyl sulfate (SDS) is effective in changing the hydrophobicity of CNTs to hydrophilicity and improving the dispersion of CNTs in aqueous solution. Enveloped with SDS, CNTs can be homogeneously mixed with Al₂O₃ at a microscopic level by heterocoagulation. This mixing method can obviously improve the chemical compatibility between CNTs and Al₂O₃, which is important for enhancement of interfacial strength between them.