Mechanical properties of silicon carbide—in situ zirconium carbonitride composites

SiC–Zr₂CN composites were fabricated by conventional hot pressing from β-SiC and ZrN powders with 2 vol% equimolar Y₂O₃–Sc₂O₃ as a sintering additive. The effects of the ZrN addition on the room-temperature (RT) mechanical properties and high-temperature flexural strength of the SiC–Zr₂CN composites were investigated. The fracture toughness gradually increased from 4.2 ± 0.3 MPa·m^1/2 for monolithic SiC to 6.3 ± 0.2 MPa·m^1/2 for a SiC–20 vol% ZrN composite, whereas the RT flexural strength (546 ± 32 MPa for the monolithic SiC) reached its maximum of 644 ± 87 MPa for the SiC–10 vol% ZrN composite. The monolithic SiC had improved strength at 1200°C, whereas the SiC–Zr₂CN composites could not retain their RT strengths at 1200°C. The typical flexural strength values of the SiC–0, 10, and 20 vol% ZrN composites at 1200°C were 650 ± 53, 448 ± 31, and 386 ± 19 MPa, whereas their RT strength values were 546 ± 32, 644 ± 87, and 528 ± 117 MPa, respectively.     

Microstructure and strengthening behavior in high content SiC nanowires reinforced SiC composites

In this study, the high-content SiC_nw reinforced SiC ceramic matrix composites (SiC_nw/SiC CMC) were successfully fabricated by hot pressing β-SiC and sintering additive (Al₂O₃-Y₂O₃) with boron nitride interphase modification SiC_nw. The effects of sintering additive content and mass fraction (5–25 wt%) of SiC_nw on the density, microstructure, and mechanical properties of the composites were investigated. The results showed that with the increase of sintering additives from 10 wt% to 12 wt%, the relative density of the SiC_nw/SiC CMC increased from 97.3% to 98.9%, attributed to the generated Y₃Al₅O₁₂ (YAG) liquid phase from the Al₂O₃-Y₂O₃ that promotes the rearrangement and migration of SiC grains. The comprehensive performance of the obtained composite with 15 wt% SiC_nw possessed the optimal flexural strength and fracture toughness of 524 ± 30.24 MPa and 12.39 ± 0.49 MPa·m^1/2, respectively. Besides, the fracture mode of the composites with 25 wt% SiC_nw content revealed a pseudo-plastic fracture behavior. It concludes that the 25 wt% SiC_nw/SiC CMC was toughened by the fiber pull-outs, debonding, bridging, and crack deflection that can consume plenty of fracture energy. The strategy of SiC nanowires worked as a main bearing phase for the fabrication of SiC/SiC CMC providing critical information for understanding the mechanical behavior of high toughness and high strength SiC nanoceramic matrix composites.     

Zirconium diboride-mullite composite form mineral: Combustion synthesis,consolidation, characterizations and properties

Zirconium diboride-mullite composite powder was synthesized in-situ by combustion in argon of a zircon sand/B₂O₃/Al reactant system in a 3 : 3: 10 M ratio. Zircon sand with a particle size less than 45 μm was activated by high-energy milling for 360 min. The optimum reactant system included the addition of 0.01 mol of Si. The product of the synthesis of this system contained 34 wt% ZrB₂ and 50 wt% mullite. The obtained zirconium diboride-mullite powder was consolidated by hot pressing at 25 MPa in an argon environment, ramping at 10 °C/min to 1,450, 1550 and 1650 °C and holding for 60 min. The sintered composite hot-pressed at 1650 °C had a density of 3.39 g/cm³, flexural strength of 153.25 ± 1.19 MPa, hardness of 10.66 GPa and fracture toughness of 4.23 MPa.m^1/2. The flexural strength and hardness of the composite was significantly influenced by the grain size of the reinforced ZrB₂. The predominantly intergranular fracture observed in surface micrographs confirmed the high toughness of the composite. The coefficient of thermal expansion of the product hot-pressed at 1650 °C was 6.53 × 10⁻⁶/°C: much lower than reported coefficients of existing Al₂O₃, ZrO₂ ZrB₂, and ZrB₂–SiC refractory ceramics.     

Mullite-bonded SiC-whisker-reinforced SiC matrix composites: Preparation,characterization, and toughening mechanisms

A novel mullite-bonded SiC-whisker-reinforced SiC matrix composite (SiCw/SiC, SiC whisker-to-SiC powder mass ratio of 1:9) was designed and successfully prepared. Before preparing the composite, the inexpensive lab-made SiCw was first modified by an oxidation/leaching process and then coated with Al₂O₃. The kinetics results indicate that the oxidation process can be described by improved shrinking-cylinder models. The aspect ratio of SiCw improved after modification. Subsequently, raw materials with a SiC–SiO₂–Al₂O₃ triple-layered structure were obtained after the Al₂O₃-coating process and used as feedstocks during the subsequent hot-pressing sintering. Finally, the characterization of the composites indicates that the mullite-bonded sample performs better (relative density of 93.8?±?1.4%, flexural strength of 533.3?±?18.2?MPa, fracture toughness of 13.6?±?2.1?MPa?m^1/2, and Vickers hardness of 20.6?±?2.5?GPa) than the reference sample without the mullite interface. The improved toughness could essentially be attributed to the moderately strong interface bonding and effective load transfer effects of the mullite interface.     

Microstructure and mechanical properties of hot pressed Al2O3/SiC nanocomposites

Al₂O₃/SiC micro/nano composites containing different volume fractions (5, 10, 15, and 20 vol.%) of SiC were prepared by mixing a sub-micron alumina powder with respective amounts of either micro- or nano-sized silicon carbide powders. The powder mixtures were hot pressed 1 h at 1740 °C and 30 MPa in the atmosphere of Ar. The effect of SiC addition on the microstructure and mechanical properties, i.e. hardness, fracture toughness, and room temperature flexural strength were investigated. The flexural strength increased with increasing volume fraction of silicon carbide particles. The maximum flexural strength (655 ± 90 MPa) was achieved for the composite containing 20 vol.% of coarse-grained SiC, which is more than twice as high as in the Al₂O₃ reference. Hardness and fracture toughness were also moderately improved. The observed improvement of mechanical properties is mainly attributed to alumina matrix grain refinement and grain boundary reinforcement.     

Hot Pressed HfB2 and HfB2–20 vol%SiC Ceramics Based on HfB2 Powder Synthesized by Borothermal Reduction of HfO2*

Phase pure hafnium diboride (HfB₂) powder was synthesized by borothermal reduction of hafnium dioxide using amorphous boron at relatively low temperature (1600°C) in vacuum. The synthesized HfB₂ powder had an average particle size of 1.37 μm with an equiaxed shape, and a low oxygen content of 0.79 wt%. Using the as-synthesized HfB₂ powder and a commercial SiC, HfB₂ monolithic, and HfB₂–20 vol%SiC composite were hot pressed at 2000°C to relative densities of 95.7% and 99.2%, respectively. With the addition of SiC, the grain size decreased and the fracture behavior changed from intergranular to a mixed mode, which resulted in a high flexural strength of 993±90 MPa for the composite. Fracture toughness of the composite was 6.29±0.65 MPa m^1/2, which was significantly higher than that of the HfB₂ monolithic and the reported values in literature.     

Processing and mechanical properties of Al2O3–5 vol.% Cr nanocomposites

The use of chromium (III) acetylacetonate as a source of nanometre sized chromium particles for the production of Al₂O₃–5 vol.% Cr nanocomposites has been investigated. The details of the processing procedure are crucial in determining the mechanical properties of the composite. The highest strength and fracture toughness, 736±29 MPa and 4.0±0.2 MPa m^1/2, respectively, were obtained for the nanocomposite hot pressed at 1450 °C. It is shown that the strengthening in Al₂O₃–5% Cr nanocomposites mainly results from microstructure refinement in that the mean alumina matrix grain size in the optimum composite was 0.68 μm compared with a grain size of 3.6 μm in the monolithic alumina hot pressed under identical conditions. Crack bridging and crack deflection by the nano-sized Cr particles did not occur to any significant extent. The slight improvement in fracture toughness may result from the observed change in fracture mode from intergranular fracture for monolithic alumina to transgranular failure for the nanocomposites.     

Fabrication and microstructure of Al2O3–ZrO2(3Y)–SiC nanocomposites

Al₂O₃–ZrO₂(3Y)–SiC composite powder was prepared by the heterogeneous precipitation method. Calcinating temperature of the powder was important to obtain dense sintered body. The nanocomposites were got by hot-pressing, and addition of ZrO₂ did not raise the sintering temperature. Some Al₂O₃ grain shape was elongated, and Al₂O₃ grain size was about μm. Nano SiC particles were observed uniformly distributing throughout the composites, and most of them were located within the matrix grains. Because SiC particles located within ZrO₂ grains influenced the phase transformation of ZrO₂, the sintering of nanocomposites, which controlled grain size and transformable ZrO₂ amount, become important to get high performance. The strength of 80 wt% Al₂O₃–15 wt% ZrO₂–5 wt% SiC nanocomposites was 555 MPa, and toughness was 3·8 MPa m^1/2, which were higher than those of monolithic Al₂O₃ ceramics. ©     

Mechanical and thermal properties of silicon carbide ceramics with yttria–scandia–magnesia

Two different SiC ceramics with a new additive composition (1.87 wt% Y₂O₃–Sc₂O₃–MgO) were developed as matrix materials for fully ceramic microencapsulated fuels. The mechanical and thermal properties of the newly developed SiC ceramics with the new additive system were investigated. Powder mixtures prepared from the additives were sintered at 1850 °C under an applied pressure of 30 MPa for 2 h in an argon or nitrogen atmosphere. We observed that both samples could be sintered to ≥99.9% of the theoretical density. The SiC ceramic sintered in argon exhibited higher toughness and thermal conductivity and lower flexural strength than the sample sintered in nitrogen. The flexural strength, fracture toughness, Vickers hardness, and thermal conductivity values of the SiC ceramics sintered in nitrogen were 1077 ± 46 MPa, 4.3 ± 0.3 MPa·m^1/2, 25.4 ± 1.2 GPa, and 99 Wm⁻¹ K⁻¹ at room temperature, respectively.     

Microstructure,mechanical properties and toughening mechanisms of graphene reinforced Al2O3-WC-TiC composite ceramic tool material

The low fracture toughness of Al₂O₃-based ceramics limited their practical application in cutting tools. In this work, graphene was chosen to reinforce Al₂O₃-WC-TiC composite ceramic tool materials by hot pressing. Microstructure, mechanical properties and toughening mechanisms of the composite ceramic tool materials were investigated. The results indicated that the more refined and denser composite microstructures were obtained with the introduction of graphene. The optimal flexural strength, Vickers hardness, indentation fracture toughness were 646.31?±?20.78?MPa, 24.64?±?0.42?GPa, 9.42?±?0.40?MPa?m^1/2, respectively, at 0.5?vol% of graphene content, which were significantly improved compared to ceramic tool material without graphene. The main toughening mechanisms originated from weak interfaces induced by graphene, and rugged fractured surface, grain refinement, graphene pull-out, crack deflection, crack bridging, micro-crack and surface peeling were responsible for the increase of fracture toughness values.     

Preparation and properties of dense ZrB2 composite reinforced by elongated SiC and Al3BC3 grains

Dense ZrB₂-SiC-Al₃BC₃ ultra-high temperature ceramic composite was fabricated by hot pressing sintering at 1900°C for 1 hour under a pressure of 20 MPa using Zirconium diboride (ZrB₂) as the raw material and a powder mixture of SiC, B₄C, Al, and carbon as the sintering additive. Al and B₄C underwent in situ reaction with carbon powder to produce Al₃BC₃, which promoted the densification of ZrB₂ ceramic. SiC grains were found to be elongated during sintering. The ZrB₂-SiC-Al₃BC₃ composite exhibited excellent mechanical properties, such as high flexural strength of 589 ± 147 MPa and fracture toughness of 7.81 ± 1.09 MPa m^1/2. Oxidation behavior of the ZrB₂-SiC-Al₃BC₃ composite was studied in air at 1500°C for 1 hour. A continuous layer of oxides consisting of a mixture of SiO₂, Al₂SiO₅, and Al₂O₃ was formed on the surface of the ZrB₂-SiC-Al₃BC₃ composite. This layer of oxides efficiently prevented oxygen from diffusing into the specimens during oxidation, which improved the oxidation resistance of the ZrB₂ ceramics.     

Joining of silicon carbide ceramics using a silicon carbide tape

This paper reports the joining of liquid-phase sintered SiC ceramics using a thin SiC tape with the same composition as base SiC material. The base SiC ceramics were fabricated by hot pressing of submicron SiC powders with 4 wt% Al₂O₃–Y₂O₃–MgO additives. The base SiC ceramics were joined by hot-pressing at 1800-1900°C under a pressure of 10 or 20 MPa in an argon atmosphere. The effects of sintering temperature and pressure were examined carefully in terms of microstructure and strength of the joined samples. The flexural strength of the SiC ceramic which was joined at 1850°C under 20 MPa, was 343 ± 53 MPa, higher than the SiC material (289 ± 53 MPa). The joined SiC ceramics showed no residual stress built up near the joining layer, which was evidenced by indentation cracks with almost the same lengths in four directions.     

Investigation of production parameters in fracture behavior of hot-pressed Al2O3–SiC/graphite fibrous monolithic ceramics: Fibers orientation and cell boundary fraction

Fibrous monoliths (FMs) exhibit graceful failure in flexure and have higher toughness values. In this research, a mixture of Al₂O₃ and SiC as the core and graphite as the shell material of fibers were produced by extrusion-molding technique and after aligning along intended directions (0°, 90°, and 0°/90°) were sintered using the hot-pressing method at the temperature of 1500°C under pressure of 35 MPa for 1 hour. The significance of fibers orientation angle and the cell to cell boundary volume ratio in defining the fracture behavior of the FMs was detected. Because of the extensive crack interactions with graphite cell boundary such as crack deflection and delamination, with increasing cell boundary content from 25 to 30 vol%, the fracture toughness was enhanced. The highest flexural strength (184.8 ± 0.61 MPa) obtained from samples with 0° fibers orientation compared to 0°/90°. Since in the transverse plies (layers with 90° aligning), the properties of matrix phase are dominant, hence the strength in specimens with 0°/90° fibers orientation decreased considerably due to weak graphite matrix phase. In addition, the fracture toughness value increased up to 8.35 ± 0.74 MPa·m^1/2 for the unidirectional architecture of (0°) in comparison with cross-ply (0°/90°) architecture.     

Preparation,mechanical properties,and toughening mechanisms of SiCw/SiCp-reinforced zirconia-toughened alumina ceramics

Zirconia-toughened alumina (ZTA) ceramics with high mechanical properties were sintered by hot-pressing method using SiC particles (SiCp) and SiC whiskers (SiCw) as the reinforcing agents simultaneously. The influences of sintering temperature, SiCp, and SiCw contents on the microstructure and mechanical properties of ZTA ceramics were investigated. It was found that both SiCp and SiCw could contribute to grain refinement significantly and promote the mechanical properties of the ceramics. However, the excess addition of SiCp or SiCw led to the formation of pores with large sizes and degraded the mechanical properties instead. When 13 wt% SiCp was introduced, the maximum flexural strength of 1180.0 MPa and fracture toughness of 15.9 MPa·m^1/2 were obtained, whereas the maximum flexural strength of 1314.0 MPa and fracture toughness of 14.7 MPa·m^1/2 were achieved at 20 wt% SiCw. Interestingly, the simultaneous addition of SiCp and SiCw could further improve the mechanical properties, and the highest flexural strength of 1334.0 MPa and fracture toughness of 16.0 MPa·m^1/2 were achieved at a SiCw/SiCp ratio of 16/4. The reinforcement mechanisms in the ceramics mainly included the phase transformation toughening of ZrO₂, the crack deflection and bridging of SiCp and SiCw, and the pull-out of SiCw.     

Architectural engineering inspired method of preparing Cf/ZrC–SiC with graceful mechanical responses

Inspired by grouting technique in architectural engineering, an innovative method of slurry injection and vacuum impregnation was put forward to introduce nanosized ZrC–SiC ceramics into PyC modified 3-D needle-punched carbon fiber preform homogeneously and continuously, followed by spark plasma sintering to prepare C_f/ZrC–SiC with graceful mechanical responses. The composite possessed improved fracture toughness and work of fracture at 5.37 ± 0.25 MPa∙m^1/2 and 951 ± 12 J/m², 50% and nearly one order of magnitude higher than those of ZrC–SiC composite, respectively, with rivaling flexural strength at 177 ± 8 MPa synchronously. A graceful fracture mode was embodied in an obviously extended yield plateau with increased failure displacement by 300%. This enhancement was attributed to the uniform and continuous combination of ZrC–SiC with carbon fiber preform as well as protection and interface tailoring from PyC coating. The study offered an easy and effective method of preparing 3-D fiber reinforced ceramic matrix composites.     

Mechanical properties of in situ synthesized mullite-based composite ceramics with three-dimensional network structure

Needle-like nanocrystalline mullite powders were prepared through the molten salt process at the temperature of 900°C using coal gangue as raw material. Then, mullite-based composite ceramics were prepared by a conventional solid-state reaction between in situ synthesized mullite and Al₂O₃ powders. Effects of Al₂O₃ content and sintering temperatures on phase compositions, microstructure, and mechanical properties of the mullite-based composite ceramics were also studied. The results show that mullite content productivity increase from 72% to 95%, as the sintering temperature increased from 1480°C to 1580°C, which led to the improvement in the bulk density and flexural strength of the samples. The three-dimensional interlocking structure for mullite-based composite ceramics was obtained by the in situ solid-state reaction process. The maximum bulk density, flexural strength, and fracture toughness for the sample with 15 wt% Al₂O₃ content are 2.48 g/cm³, 139.79 MPa, and 5.62 MPa··m^1/2, respectively, as it was sintered at the temperature of 1560°C for 3 h. The improved mechanical properties of mullite-based composite ceramics maybe ascribed to good densification and increased mullite phase content, as well as to the in situ three-dimensional network structure. Therefore, the results would provide new ideas for high-value utilization of coal gangue.     

Direct bonding of silicon carbide ceramics sintered with yttria

SiC ceramics sintered with yttria were successfully joined without an interlayer by conventional hot pressing at lower temperatures (2000–2050 °C) compared to those of the sintering temperatures (2050–2200 °C). The joined SiC ceramics sintered with 2000 ppm Y₂O₃ showed almost the same thermal conductivity (˜198 Wm⁻¹ K⁻¹), fracture toughness (3.7 ± 0.2 MPa m^1/2), and hardness (23.4 ± 0.8 GPa) as those of the base material, as well as excellent flexural strength (449 MPa). In contrast, the joined SiC ceramics sintered with 4 wt% Y₂O₃ showed very high thermal conductivity (˜204 Wm⁻¹ K⁻¹) and excellent flexural strength (˜505 MPa). Approximately 16–22% decreases in strength compared to those of the base SC materials were observed in both joined ceramics, due to the segregation of liquid phase at the interface. This issue might be overcome by preparing well-polished and highly flat surfaces before joining.     

Fabrication and characterization of SiC-ZTA ceramic composites by hot pressing

Al₂O₃/ZrO₂/SiC ceramic composites with different SiC contens have been prepared by hot pressuring. The effect of SiC content on the microstructure and mechanical properties of composites have been studied. The results show that SiC has obvious grain refinement effect on ZTA ceramics and change the fracture mode of the matrix from intergranular fracture to transgranular fracture. Simultaneously, it has been found that the mechanical properties of the material are significantly enhanced in comparison with ZTA matrix. The highest strength is acquired at 10% SiC content, the flexural strength and toughness are obtained when the SiC content is 15 vol%, and the values are 18.86 GPa, 1262 MPa and 6.13 MPa m^1/2, respectively. The mechanisms of hardening, strengthening and toughening have been discussed.     

Thermal and Mechanical Properties of SiC–TiC0.5N0.5 Composites

SiC–TiC_0.5N_0.5 composites were fabricated from β‐SiC and TiN powders with 2 vol% equimolar Y₂O₃–Sc₂O₃ additives by conventional hot pressing. Thermal and mechanical properties of the SiC–TiC_0.5N_0.5 composites were investigated as a function of initial TiN content. Relative densities of ≥98.9% were achieved for all samples. The addition of a small amount of TiN increased thermal conductivity, flexural strength, and fracture toughness of SiC ceramics. However, further addition of TiN in excess of 10 and 20 vol% deteriorated both thermal conductivity and flexural strength of the composites, respectively. In contrast, the fracture toughness of the composites increased continuously from 4.2 to 6.2 MPa?m^1/2 with increasing initial TiN content from 0 to 35 vol%, due to crack deflection by TiC_0.5N_0.5. The maximum values of thermal conductivity and flexural strength were 224 W/m K for a 2 vol% TiC_0.5N_0.5 and 599 MPa for a 10 vol% TiC_0.5N_0.5 composite.     

Mechanical performance and microstructure of 3Y-TZP/Al2O3/GNPs medical ceramic surgical scalpel material prepared through SPS–HF dual sintering method

In this study, 3 mol% yttria-stabilized tetragonal zirconia polycrystal (3Y-TZP)/Al₂O₃/graphene nanoplatelets (GNPs) medical ceramic materials for manufacturing surgical scalpels were sintered in vacuum in an SPS–625HF furnace. The mechanical performances and microstructures of the composites were investigated, and the influence mechanisms of the sintering temperature and amount of added GNPs were studied. During the sintering process at 1400°C and 30 MPa for 5 min, the added GNPs enhanced the mechanical properties of the 3Y-TZP/Al₂O₃ composites. The results showed that the composite with .1 wt.% GNPs had 6.4% (910 ± 11 MPa) higher flexural strength than 3Y-TZP/Al₂O₃. The composite with .4 wt.% GNPs had 38.7% (12.95 ± .22 MPa m^1/2) greater fracture toughness than 3Y-TZP/Al₂O₃. The main toughening mechanisms of 3Y-TZP/Al₂O₃/GNPs were crack bridging, crack deflection, crack branching, GNPs bridging, transgranular fracture structures, and phase transformation of t-ZrO_1.95. The two-stage densification displacement curve appeared at the optimal sintering temperature of the materials, and the 3Y-TZP/Al₂O₃/GNPs composites with a two-stage densification displacement curve had excellent mechanical properties. The added GNPs can inhibit the grain growth during the sintering process, thereby refining the zirconia grains. With the increase in GNPs content, the grain size and flexural strength of the composites decreased gradually. However, higher content of GNPs was beneficial to improve the relative density and thermal diffusivity of 3Y-TZP/Al₂O₃/GNPs composite material.