Microstructure and Property Characterization of Sintered Si3N4, SiC, and SiAlON

Commercially produced pressureless sintered Si₃N₄, SiC, and SiAlON were characterized with respect to density, phases present, bend strength, and oxidation resistance. The room-temperature bend strengths of sintered Si₃N₄, SiC, and SiAlON are comparable. However, the room-temperature strengths are much lower (=40 to 50%) than the room-temperature strength of hot–pressed Si₃N₄ (NC-132). The strength loss in Si₃N₄ and SiAlON materials at high temperature was attributed to a viscous grain-boundary phase retained during cooling from the sintering temperature. The oxidation resistance of sintered a-SiC was the best of any materials tested.     

Delayed-Failure Resistance of High-Purity Si3N4 at 1400°C

Delayed failure and creep behavior of high-purity Si₃N₄ sintered without additives with a mean grain size of 1 μm has been measured at 1400°C. Lifetime under 300 MPa was >240 h, which showed good agreement with the value predicted in our previous report. Creep strain rate ranged from 1 × 10⁻⁵ to 3 × 10⁻⁵ h⁻¹ between 200 and 360 MPa. These values demonstrate the excellent potential of high-purity Si₃N₄ materials for structural application up to 1400°C.     

Pressureless Sintering of Dense Si3N4 and Si3N4/SiC Composites with Nitrate Additives

The effect of aluminum and yttrium nitrate additives on the densification of monolithic Si₃N₄ and a Si₃N₄/SiC composite by pressureless sintering was compared with that of oxide additives. The surfaces of Si₃N₄ particles milled with aluminum and yttrium nitrates, which were added as methanol solutions, were coated with a different layer containing Al and Y from that of Si₃N₄ particles milled with oxide additives. Monolithic Si₃N₄ could be sintered to 94% of theoretical density (TD) at 1500°C with nitrate additives. The sintering temperature was about 100°C lower than the case with oxide additives. After pressureless sintering at 1750°C for 2 h in N₂, the bulk density of a Si₃N₄/20 wt% SiC composite reached 95% TD with nitrate additives.     

Impurity-Enhanced Intergranular Cavity Formation in Silicon Nitride at High Temperatures

The effect of trace impurities on high-temperature strength is examined in Si₃N₄ sintered without additives. Strength degradation above 1000°C occurs only in the low-purity material, which also exhibits an intergranular slow crack growth (SCG) rate 2 orders of magnitude faster than that of the high-purity material at 1400°C. A relaxation peak of internal friction is observed only in the low-purity material, at ≅1200°C, and the origin of this peak is ascribed to the initial stage of SCG—that is, the cavity-nucleation stage, enhanced by impurities. Based on the present results, a model for impurity-enhanced SCG is proposed.     

Burner Rig Hot Corrosion of Silicon Carbide and Silicon Nitride

A number of commercially available SiC and Si₃N₄ materials were exposed to 1000°C for 40 h in a high-velocity, pressurized burner rig as a simulation of an aircraft turbine environment. Na impurities (2 ppm) added to the burner flame resulted in molten Na₂SO₄ deposition, attack of the SiC and Si₃N₄, and formation of substantial Na₂O. x (SiO₂) corrosion product. Room-temperature strength of the materials decreased as a result of the formation of corrosion pits in SiC and grain-boundary dissolution and pitting in Si₃N₄.     

Combustion Synthesis of Si3N4–SiC Composite Powders

Fine Si₃N₄-SiC composite powders were synthesized in various SiC compositions to 46 vol% by nitriding combustion of silicon and carbon. The powders were composed of α-Si₃N₄, β-Si₃N₄, and β-SiC. The reaction analysis suggested that the SiC formation is assisted by the high reaction heat of Si nitridation. The sintered bodies consisted of uniformly dispersed grains of β-Si₃N₄, β-SiC, and a few Si₂N₂O.     

Influence of Rare-Earth Additives on Wear Properties of Hot-Pressed Silicon Nitride Ceramics under Dry Sliding Conditions

The influence of different rare-earth sintering additives (Y, Yb, Lu) on the wear properties of Si₃N₄ ceramics was investigated during sliding contact without lubricant. The kind of rare-earth additives was shown to have a significant effect on the wear behavior for contact sliding under the present testing conditions. Samples sintered with Y₂O₃ as the sintering additive showed evidence of fracture type wear although this was not observed in samples sintered with Yb₂O₃ and Lu₂O₃. These smaller rare earths lead to higher grain boundary bonding strength and superior high-temperature properties and resulted in higher wear resistance. These results showed that the wear properties of Si₃N₄ ceramics could be tailored by judicious selection of the sintering additives.     

Molten-Salt Corrosion of Silicon Nitride: I, Sodium Carbonate

Corrosion of Si₃N₄ under thin films of Na₂CO₃ was investigated at 1000°C. Pure Si₃N₄ and Si₃N₄ with various additives were examined. Thermogravimetric analysis and morphology observations lead to the following detailed reaction mechanism: (I) decomposition of Na₂CO₃ and formation of Na₂SiO₃, (II) rapid oxidation, and (III) formation of a protective silica layer below the silicate and a slowing of the reaction. For Si₃N₄ with Y₂O₃ additions, preferential attack of the grain-boundary phase occurred. The corrosion of pure Si and SiC was also studied for comparison to Si₃N₄. The corrosion mechanism generally applies to all three materials. Silicon reacted substantially faster than Si₃N₄ and SiC.     

Spherical-Impact Damage and Strength Degradation in Silicon Carbide Whisker/Silicon Nitride Composites

The silicon carbide (SiC) whisker reinforcement of silicon nitride (Si₃N₄) improves fracture strength and toughness, hardness, and Young's modulus, resulting in higher resistance of the composites to sphere penetration and crack initiation at spherical impact. Sintered Si₃N₄ shows an elastic/plastic response and initiates median/radial cracks at 100 m/s impact velocity. SiC-whisker/Si₃N₄ composites, on the other hand, demonstrate an elastic response, with Hertzian cone crack initiation, only when impact velocity exceeds 280 m/s. The SiC-whisker/Si₃N₄ composites thus exhibit improved strength degradation versus critical impact velocity characteristics because of improved mechanical properties provided by the SiC whiskers.     

Evaluation of Glassy Phase in Sintered Silicon Nitride by Low-Temperature Specific Heat Measurements

The specific heat of HIP sintered Si₃N₄ with 3 mol% Y₂O₃ and 3 mol% Al₂O₃ additives was measured at different temperatures ranging from 2 to 10 K, in order to confirm the presence of a glassy phase in the sintered body. The grainboundary glassy phase in the sintered Si₃N₄ was evaluated by specific heat measurements. The difference between the experimental value and the lattice specific heat calculated from the Debye theory confirmed the existence of a glassy phase in sintered Si₃N₄.     

Silicon Carbide Monofilament-Reinforced Silicon Nitride or Silicon Carbide Matrix Composites

SiC-monofilament-reinforced SiC or Si₃N₄ matrix composites were fabricated by hot-pressing, and their mechanical properties and effects of filaments and filament coating layers were studied. Relationships between frictional stress of filament/matrix interface and fracture toughness of SiC monofilament/Si₃N₄ matrix composites were also investigated. As a result, it was confirmed experimentally that in the case of composites fractured with filament pullout, the fracture toughness increased as the frictional stress increased. On the other hand, when frictional stress was too large (>about 80 MPa) for the filament to be pulled out, fracture toughnesses of the composites were almost the same and not so much improved over that of Si₃N₄ monolithic ceramics. The filament coating layers were found to have a significant effect on the frictional stress of the SiC monofilament/Si₃N₄ matrix interface and consequently the fracture toughness of the composites. Also the crack propagation behavior in the SiC monofilament/Si₃N₄ matrix composites was observed during flexural loading and cyclic loading tests by an in situ observation apparatus consisting of an SEM and a bending machine. The filament effect which obstructed crack propagation was clearly observed. Fatigue crack growth was not detected after 300 cyclic load applications.     

Molten-Salt Corrosion of Silicon Nitride: II, Sodium Sulfate

The corrosion mechanism of Si₃N₄+ Na₂SO₄/O₂ at 1000°C was investigated. Corrosion of both pure and additive-containing Si₃N₄ was studied. The reaction of Si₃N₄+ Na₂SO₄ consists of an initial period of slow weight loss due to Na₂SO₄ vaporization and oxidation-dissolution. This initial period was the same for all forms of Si₃N₄. A second region consisted of further oxidation or near termination of reaction, depending on the additive in the Si₃N₄. A 5- to 10-μm yttrium depletion zone was found after corrosion for the Si₃N₄ with yttria additives. For comparison, Si and SiC were corroded under similar conditions. These materials corroded substantially faster than all forms of Si₃N₄.     

Role of Si2N2O in the Passive Oxidation of Chemically-Vapor-Deposited Si3N4

The results of two-step oxidation experiments on chemically-vapor-deposited Si₃N₄ and SiC at 1350°C show that a correlation exists between the presence of a Si₂N₂O interphase and the strong oxidation resistance of Si₃N₄. During normal oxidation, k _p for SiC was 15 times higher than that for Si₃N₄, and the oxide scale on Si₃N₄ was found by SEM and TEM to contain a prominent Si₂N₂O inner layer. However, when oxidized samples are annealed in Ar for 1.5 h at 1500°C and reoxidized at 1350°C as before, three things happen: the oxidation k _p increases over 55-fold for Si₃N₄, and 3.5-fold for SiC; the Si₃N₄ and SiC oxidize with nearly equal k _p's; and, most significant, the oxide scale on Si₃N₄ is found to be lacking an inner Si₂N₂O layer. The implications of this correlation for the competing models of Si₃N₄ oxidation are discussed.     

Stepwise-Graded Si3N4–SiC Ceramics with Improved Wear Properties

The processing of stepwise graded Si₃N₄/SiC ceramics by pressureless co-sintering is described. Here, SiC (high elastic modulus, high thermal expansion coefficient) forms the substrate and Si₃N₄ (low elastic modulus, low thermal expansion coefficient) forms the top contact surface, with a stepwise gradient in composition existing between the two over a depth of ∼1.7 mm. The resulting Si₃N₄ contact surface is fine-grained and dense, and it contains only 2 vol% yttrium aluminum garnet (YAG) additive. This graded ceramic shows resistance to cone-crack formation under Hertzian indentation, which is attributed to a combined effect of the elastic-modulus gradient and the compressive thermal-expansion-mismatch residual stress present at the contact surface. The presence of the residual stress is corroborated and quantified using Vickers indentation tests. The graded ceramic also possesses wear properties that are significantly improved compared with dense, monolithic Si₃N₄ containing 2 vol% YAG additive. The improved wear resistance is attributed solely to the large compressive stress present at the contact surface. A modification of the simple wear model by Lawn and co-workers is used to rationalize the wear results. Results from this work clearly show that the introduction of surface compressive residual stresses can significantly improve the wear resistance of polycrystalline ceramics, which may have important implications for the design of contact-damage-resistant ceramics.     

Texture Development in Silicon Nitride–Silicon Oxynitride In Situ Composites via Superplastic Deformation

Silicon nitride–silicon oxynitride (Si₃N₄–Si₂N₂O) in situ composites have been fabricated via either the annealing or the superplastic deformation of sintered Si₃N₄ that has been doped with a silica-containing additive. In this study, quantitative texture measurements, including pole figures and X-ray diffraction patterns, are used in conjunction with scanning electron microscopy and transmission electron microscopy techniques to examine the degree of preferred orientation and texture-development mechanisms in these materials. The results indicate that (i) only superplastic deformation can produce strong textures in the β-Si₃N₄ matrix, as well as Si₂N₂O grains that are formed in situ ; (ii) texture development in the β-Si₃N₄ matrix mainly results from grain rotation via grain-boundary sliding; and (iii) for Si₂N₂O, a very strong strain-dependent texture occurs in two stages, namely, preferred nucleation and anisotropic grain growth.     

Mechanical Properties of Si2N2O/SiC-Whisker Composites

The mechanical and thermal properties of Si₂N₂O/SiC-whisker composites were studied with emphasis on the effect of matrix composition and of whisker content. The fracture toughness of Si₂N₂O was remarkably improved by 90% with a concomitant 70% strength improvement by addition of SiC whiskers of only 10 vol%. Optimum mechanical and thermal properties of Si₂N₂O/SiC-whisker composites were obtained at an equimolar ratio of Si₃N₄/SiO₂, which is the stoichiometric composition for Si₂N₂O. Additional investigation concerning the Si₂N₂O-matrix/SiC-whisker interface by controlling sintering additives is necessary for further improvement of mechanical and thermal properties of Si₂N₂O/SiC-whisker composites.     

In Situ Polysilane-Derived Silicon Carbide Particulates Dispersed in Silicon Nitride Composite

A dense (97% of theoretical density) Si₃N₄—SiC composite containing 10 wt%β-SiC was prepared by introducing a SiC phase by the pyrolysis of a polymeric SiC precursor. The composite material was produced by mixing an alkyl/aryl-substituted polysilane with Si₃N₄ powder and, by subsequently forming green compacts, pyrolyzing the polymeric species, and finally sintering the sample. Synthesis and characterization of the polymeric compound was described. Its transformation reactions to SiC and the characterization of the ceramic residue were also studied. High ceramic yields were obtained by curing the as-synthesized polysilane at 500°C in an Ar atmosphere. The heat treatment had no effect on the good solubility of the polymeric precursor in organic solvents. This was important for processes such as infiltration, sealing, and coating and for the mixing of the polymer with powders for the preparation of homogeneous composite ceramics. The dense microstructure of the pyrolyzed and sintered Si₃N₄ powder–polysilane mixture exhibited reduced grain growth of the Si₃N₄ particles and a very homogeneous distribution of the in situ-formed β-SiC phase.     

Reactivity of Aluminum Nitride Powder in Aqueous Silicon Nitride and Silicon Carbide Slurries

The reactivity of AlN powder with water in supernatants obtained from centrifuged Si₃N₄ and SiC slurries was studied by monitoring the pH versus time. Various Si₃N₄ and SiC powders were used, which were fabricated by different production routes and had surfaces oxidized to different degrees. The reactivity of the AlN powder in the supernatants was found to depend strongly on the concentration of dissolved silica in these slurries relative to the surface area of the AlN powder in the slurry. The hydrolysis of AlN did not occur if the concentration of dissolved silica, with respect to the AlN powder surface, was high enough (1 mg SiO₂/(m² AlN powder)) to form a layer of aluminosilicates on the AlN powder surface. This assumption was verified by measuring the pH of more concentrated (31 vol%) Si₃N₄ and SiC suspensions also including 5 wt% of AlN powder (with respect to the solids).     

Fabrication of Low-Shrinkage, Porous Silicon Nitride Ceramics by Addition of a Small Amount of Carbon

Successful net-shape sintering offers a significant advantage for producing large or complicated products. Porous Si₃N₄ ceramics with very low shrinkage were developed, in the present investigation, by the addition of a small amount of carbon. Carbon powders (1–5 vol%) of two types, with different mean particle sizes (13 nm and 5 μm), were added to α-Si₃N₄−5 wt% Y₂O₃ powders. SiC nanoparticles formed through reaction of the added carbon with SiO₂ on the Si₃N₄ surface or with the Si₃N₄ particles themselves. Such reaction-formed SiC nanoparticles apparently had an effective reinforcing effect, as in nanocomposites. Sintered Si₃N₄ porous ceramics with a high porosity of 50%–60%, a very small linear shrinkage of ∼2%–3%, and a strength of ∼100 MPa were obtained.     

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.