R-Curve Behavior of Si3N4–BN Composites

R -curve behavior of Si₃N₄–BN composites and monolithic Si₃N₄ for comparison was investigated. Si₃N₄–BN composites showed a slowly rising R -curve behavior in contrast with a steep R -curve of monolithic Si₃N₄. BN platelets in the composites seem to decrease the crack bridging effects of rod-shaped Si₃N₄ grains for small cracks, but enhanced the toughness for long cracks as they increased the crack bridging scale. Therefore, fracture toughness of the composites was relatively low for the small cracks, but it increased significantly to ∼8 MPa·m^1/2 when the crack grew longer than 700 μm, becoming even higher than that of the monolithic Si₃N₄.     

Effect of the Amount of Additives and Post-Heat Treatment on the Microstructure and Mechanical Properties of Yttrium–α-Sialon Ceramics

The yttrium–sialon ceramics with the composition of Y_0.333Si₁₀Al₂ON₁₅ and an excess addition of Y₂O₃ (2 or 5 wt%) were fabricated by hot isostatic press (HIP) sintering at 1800°C for 1 h. The resulting materials were subsequently heat-treated in the temperature range 1300–1900°C to investigate its effect on the α→β-sialon phase transformation, the morphology of α-sialon grains, and mechanical properties. The results show that α-sialons stabilized by yttrium have high thermal stability. An adjustment of the α-sialon phase composition is the dominating reaction in the investigated Y–α-sialon ceramics during low-temperature annealing. Incorporation of excess Y₂O₃ could effectively promote the formation of elongated α-sialon grains during post-heat-treating at relatively higher temperature (1700° and 1900°C) and hence resulted in a high fracture toughness ( K _IC= 6.3 MPa·m^1/2) via grain debonding and pullout effects. Although the addition of 5 wt% Y₂O₃ could promote the growth of elongated α grains with a higher aspect ratio, the higher liquid-phase content increased the interfacial bonding strength and therefore hindered interface debonding and crack deflection. The heat treatment at 1500°C significantly changed the morphology of α-sialon grains from elongated to equiaxed and hence decreased its toughness.     

Superplastic Deformation in Silicon Nitride–Silicon Oxynitride In Situ Composites

Starting with a mixture of ultrafine β-Si₃N₄ and a SiO₂-containing additive, a superplastic Si₃N₄-based composite was developed, using the concept of a transient liquid phase. Significant deformation-induced phase and microstructure evolutions occurred in the nonequilibrium, fine-grained Si₃N₄ material, which led to the in situ development of a Si₃N₄–22-vol%-Si₂N₂O composite and strong texture formation. The unusual ductility of the composites with elongated Si₂N₂O grains was attributed to the fine-grained microstructure, the presence of a transient liquid phase, and the alignment of the elongated Si₂N₂O grains. The mechanical properties of the resultant composite were enhanced rather than impaired by superplastic deformation and subsequent heat treatment; the resultant composite exhibited both high strength (957 MPa) and high fracture toughness (4.8 MPa·m^1/2).     

Effect of Grain Size on the Thermal Conductivity of Si3N4

Polycrystalline Si₃N₄ samples with different grain-size distributions and a nearly constant volume content of grain-boundary phase (6.3 vol%) were fabricated by hot-pressing at 1800°C and subsequent HIP sintering at 2400°C. The HIP treatment of hot-pressed Si₃N₄ resulted in the formation of a large amount of ß-Si₃N₄ grains ∼10 µm in diameter and ∼50 µm long, and the elimination of smaller matrix grains. The room-temperature thermal conductivities of the HIPed Si₃N₄ materials were 80 and 102 Wm⁻¹K⁻¹, respectively, in the directions parallel and perpendicular to the hot-pressing axis. These values are slightly higher than those obtained for hot-pressed samples (78 and 93 Wm⁻¹K⁻¹). The calculated phonon mean free path of sintered Si₃N₄ was ∼20 nm at room temperature, which is very small as compared to the grain size. Experimental observations and theoretical calculations showed that the thermal conductivity of Si₃N₄ at room temperature is independent of grain size, but is controlled by the internal defect structure of the grains such as point defects and dislocations.     

Reaction-Bonded and Superplastically Sinter-Forged Silicon Nitride–Silicon Carbide Nanocomposites

Silicon nitride–silicon carbide (Si₃N₄–SiC) nanocomposites were fabricated by a process involving reaction bonding followed by superplastic sinter-forging. The nanocomposites exhibited an anisotropic microstructure, in which rod-shaped, micrometer-sized Si₃N₄ grains tended to align with their long axes along the material-flow direction. SiC particles, typically measuring several hundred nanometers, were located at the Si₃N₄ grain boundaries, and nanosized particles were dispersed inside the Si₃N₄ grains. A high bending strength of 1246 ± 119 MPa, as well as a high fracture toughness of 8.2 ± 0.9 MPa·m^1/2, was achieved when a stress was applied along the grain-alignment direction.     

Self-Reinforced Nitrogen-Rich Calcium–α-SiAlON Ceramics

Nitrogen-rich Ca–α-SiAlON ceramics with nominal compositions Ca _x Si_{12−2 x} Al_{2 x} N₁₆ and 0.2≤ x ≤2.6, extending along the Si₃N₄–1/2Ca₃N₂:3AlN tie line, were prepared from Si₃N₄, AlN, and CaH₂ precursors by hot pressing at 1800°C. The x values attained were determined by energy-dispersive X-ray (EDX) microanalysis and X-ray powder diffraction (XRPD) data using the Rietveld method. The results show that Ca–α-SiAlONs form continuously within the compositional range x =0 to at least x =1.82. Phase assemblages, lattice parameters, Vickers hardness, and fracture toughness were determined and correlated to the calcium content, x . Owing to a high sintering temperature and the use of CaH₂ as a precursor, grain growth was kinetically enhanced, resulting in self-reinforced microstructures with elongated grains. The obtained Ca–α-SiAlON ceramics demonstrate a combination of both high hardness ∼21 GPa, and high fracture toughness ∼5.5 MPa·m^1/2.     

Fracture Energies of Tape-Cast Silicon Nitride with β-Si3N4 Seed Addition

The fracture energies of the tape-cast silicon nitride with and without 3 wt% rod-like β-Si₃N₄ seed addition were investigated by a chevron-notched-beam technique. The material was doped with Lu₂O₃–SiO₂ as sintering additives for giving rigid grain boundaries and good heat resistance. The seeded and tape-cast silicon nitride has anisotropic microstructure, where the fibrous grains grown from seeds were preferentially aligned parallel to the casting direction. When a stress was applied parallel to the fibrous grain alignment direction, the strength measured at 1500°C was 738 MPa, which was almost the same as room temperature strength 739 MPa. The fracture energy of the tape-cast Si₃N₄ without seed addition was 109 and 454 J/m² at room temperature and 1500°C, respectively. On the contrary, the fracture energy of the seeded and tape-cast Si₃N₄ was 301 and 781 J/m² at room temperature and 1500°C, respectively, when a stress was applied parallel to the fibrous gain alignment. The large fracture energies were attributable primarily to the unidirectional alignment fibrous Si₃N₄ grains.     

Precursor-Derived Si-B-C-N Ceramics: Oxidation Kinetics

The oxidation behavior of three precursor-derived ceramics—Si_4.46BC_7.32N_4.40 (AMF2p), Si_2.72BC_4.51N_2.69 (AMF3p), and Si_3.08BC_4.39N_2.28 (T2/1p)—was investigated at 1300° and 1500°C. Scale growth at 1500°C in air can be approximated by a parabolic rate law with rate constants of 0.0599 and 0.0593 μm²/h for AMF3p and T2/1p, respectively. The third material does not oxidize according to a parabolic rate law, but has a similar scale thickness after 100 h. The results show that at least within the experimental times these ceramics develop extremely thin scales, thinner than pure SiC or Si₃N₄.     

Effect of Sintering Additives on Microstructure and Mechanical Properties of Porous Silicon Nitride Ceramics

Porous silicon nitride (Si₃N₄) ceramics with about 50% porosity were fabricated by pressureless sintering of α-Si₃N₄ powder with 5 wt% sintering additive. Four types of sintering aids were chosen to study their effect on the microstructure and mechanical properties of porous Si₃N₄ ceramics. XRD analysis proved the complete formation of a single β-Si₃N₄ phase. Microstructural evolution and mechanical properties were dependent mostly on the type of sintering additive. SEM analysis revealed the resultant porous Si₃N₄ ceramics as having high aspect ratio, a rod-like microstructure, and a uniform pore structure. The sintered sample with Lu₂O₃ sintering additive, having a porosity of about 50%, showed a high flexural strength of 188 MPa, a high fracture toughness of 3.1 MPa·m^1/2, due to fine β-Si₃N₄ grains, and some large elongated grains.     

Mechanical Properties and Contact Damage Behavior in Aligned Silicon Nitride Materials

Aligned Si₃N₄ microstructures were achieved by seeding, extruding, and laminating methods. The degree of grain alignment was determined by microstructural measurements. Mechanical properties, including toughness, strength, hardness, and elastic modulus, as well as the contact damage response, were addressed and discussed as a function of this anisotropic microstructure. K _{I C} values over 8 MPa·m^1/2 and strengths above 900 MPa were achieved for the most favorable planes in the textured material. Contact damage behavior was influenced by grain orientation in two ways, first, by conferring elliptical shape to the radial surface cracks and second, by the multiple twin/slip formation at the large seeds within the high shear strain region.     

Influence of Planetary High-Energy Ball Milling on Microstructure and Mechanical Properties of Silicon Nitride Ceramics

The influence of ball-milling methods on microstructure and mechanical properties of silicon nitride (Si₃N₄) ceramics produced by pressureless sintering for a sintering additive from MgO–Al₂O₃–SiO₂ system was investigated. For planetary high-energy ball milling, the mechanical properties of Si₃N₄ ceramics were evidently improved and a homogeneous microstructure developed. In contrast, some exaggerated elongated grains were developed due to the local enrichment of sintering additives in the specimen prepared by general ball milling. For Si₃N₄ ceramics produced by planetary ball milling, flexure strength of 1.06 GPa, Vickers hardness of 14.2 GPa, and fracture toughness of 6.6 MPa·m^0.5 were achieved. The differences in the mechanical properties of Si₃N₄ ceramics produced by different processing seem to arise mainly from the changes in microstructural homogenization and sinterability. The planetary high-energy ball-milling process provides a good route to mix starting powders for developing ceramics with uniform microstructure and promising mechanical properties.     

Fabrication and Characterization of Three-Dimensional Carbon Fiber Reinforced Silicon Carbide and Silicon Nitride Composites

Three-dimensional (3D) carbon fiber reinforced SiC and Si₃N₄ composites have been fabricated using repeated infiltration of an organosilicon slurry under vacuum and pressure. Open porosity of the infiltrated body was reduced from 40% after the first infiltration to approximately 8% after the seventh cycle. Further reduction of open porosity to less than 3% was accomplished by hot-press densification. The maximum values of flexural strength and fracture toughness were, respectively, 260 MPa and 7.3 MPa·m^1/2for C/Si₃N₄ composites, and 185 MPa and 6 MPa·m^1/2 for C/SiC composite.     

Fabrication of Reaction-Sintered Sialon

A factorial design experiment was conducted to determine the major parameters affecting the densification of mixtures having the composition (in mol%) 50 Si₃N₄, 25 A1₂O₃, and 25 A1N. Improved densities of the resulting sialon were achieved using a longer milling time and SN-502 Si₃N₄ powder. However, sialon samples prepared from the SN-502 powder contained some of the X-phase, whereas those fabricated from AME Si₃N₄ powder did not. This difference is considered to be due to the higher SiO₂ content of the SN-502 powder and its greater susceptibility to partial hydrolysis during the milling process. Reaction-sintered sialon (97.2% theoretical density) fabricated using AME powder had a room-temperature bend strength of 352
MN/m² (51,000 psi) and exhibited slow crack growth at 1300° and 1400°C. It is suggested that this is not an inherent property of sialon but is due to the presence of a calcium-containing grain-boundary phase, as in hot-pressed Si₃N₄.     

Method to Estimate Crack-Tip Toughness from Bending Tests on Prenotched Bars

A strain-gauge procedure that enables determination of the crack-tip toughness ( K _I0) from bending-strength tests is described. The procedure is applied to coarse-grained alumina and yields an average K _I0 value of 2.51 MPa·m^1/2, with a standard deviation of 0.16 MPa·m^1/2.     

R-Curve for a Lead Zirconate Titanate Ceramic Obtained from Tensile Strength Tests with Knoop-Damaged Specimens

A procedure was used that made it possible to determine the R -curve for piezoelectric ceramics from tensile strength tests conducted with Knoop-damaged specimens. The resulting crack-tip toughness K _I0 was 0.6 MPa·m^1/2, and the R -curve starting from this value increased to 1.4 MPa·m^1/2 within a 0.7 mm crack extension.     

Microstructure and Mechanical Properties of the in situβ-Si3N4/α'-SiAlON Composite

The in situ β-Si₃N₄/α'-SiAlON composite was studied along the Si₃N₄–Y₂O₃: 9 AlN composition line. This two phase composite was fully densified at 1780°C by hot pressing Densification curves and phase developments of the β-Si₃N₄/α'-SiAlON composite were found to vary with composition. Because of the cooperative formation of α'-Si AlON and β-Si₃N₄ during its phase development, this composite had equiaxed α'-SiAlON (∼0.2 μm) and elongated β-Si₃N₄ fine grains. The optimum mechanical properties of this two-phase composite were in the sample with 30–40%α', which had a flexural strength of 1100 MPa at 25°C 800 MPa at 1400°C in air, and a fracture toughness 6 Mpa·m^1/2. α'-SiAlON grains were equiaxed under a sintering condition at 1780°C or lower temperatures. Morphologies of the α°-SiAlON grains were affected by the sintering conditions.     

Threshold Stress Intensity for Crack Growth in Silicon Carbide Ceramics

Measurements of threshold stress intensities for crack growth, K _h, of three polycrystalline SiC materials were attempted using interrupted static fatigue tests at 1200°–1400°C. Weibull statistics were used to calculate conservative K_th values from test results. The K _th of a chemically vapor deposited β-SiC could not be determined, as a result of its wide variations in strength. The K_th ≥ 3.3,2.2, and 1.7 MPa·m^1/2 for an Al-doped sintered α-SiC; and K_th ≥ 3.1, 2.7, and 2.2 MPa·m^1/2 for a hot isostatically pressed α-SiC, both at 1200°, 1300°, and 1400°C, respectively. A damage process concurrent with subcritical crack growth was apparent for the sintered SiC at 1400°C. The larger K_th 's for the HIPed SiC (compared to the sintered SiC) may be a result of enhanced viscous stress relaxation caused by the higher silica content and smaller grain size of this material. Values measured at 1300° and 1400°C were in good agreement with the K_th's predicted by a diffusive crack growth model, while the measured K_th 's were greater than the predicted ones at 1200°C.     

Microstructure and Properties of Self-Reinforced Silicon Nitride

Problems associated with manufacturing Si₃N₄/SiC-whisker composites have been overcome by developing selfreinforced Si₃N₄ with elongated β-Si₃N₄ grains formed in situ from oxynitride glass. This Si₃N₄–Y₂O₃–MgO–SiO₂–CaO-based material has a flexure strength >1000 MPa and fracture toughness >8 MPa·m^½. The optimum combination of mechanical properties has been obtained with Y₂O₃:MgO ratios ranging from 3:1 to 1:2, CaO contents ranging from 0.1 to 0.5 wt%, and Si₃N₄ contents between 90 and 96 wt%.     

Layered Silicon Nitride-Based Composites with Discontinuous Boron Nitride Interlayers

The influence of a strong/weak interface ratio on the mechanical properties of Si₃N₄/BN-based layered composites was studied. The ratio was controlled by the number of BN spots between the adjacent Si₃N₄ layers. By increasing the BN interface area from 0% to 72%, fracture toughness increased from 7.7 to 10.9 MPa·m^1/2, and bending strength decreased from 1275 to 982 MPa. Fracture toughness was improved from 8.6 to 10.1 MPa·m^1/2 by additional heat treatment of samples containing 2 vol%β-Si₃N₄ seed particles. The bending strength of samples with 35% weak BN interfaces, measured perpendicular and parallel to layer alignment, was 1260 and 1240 MPa, respectively. This confirmed the two-directional isotropy of layered samples.     

Microstructure and Mechanical Properties of Hot-Pressed α-Al2O3-Seeded γ-Alumina Ceramics

High-quality alumina ceramics were fabricated by a hot pressing with MgO and SiO₂ as additives using α-Al₂O₃-seeded nanocrystalline γ-Al₂O₃ powders as the raw material. Densification behavior, microstructure evolution, and mechanical properties of alumina were investigated from 1250°C to 1450°C. The seeded γ-Al₂O₃ sintered to 98% relative density at 1300°C. Obvious grain growth was observed at 1400°C and plate-like grains formed at 1450°C. For the 1350°C hot-pressed alumina ceramics, the grain boundary regions were generally clean. Spinel and mullite formed in the triple-grain junction regions. The bending strength and fracture toughness were 565 MPa and 4.5 MPa·m^1/2, respectively. For the 1300°C sintered alumina ceramics, the corresponding values were 492 MPa and 4.9 MPa·m^1/2.