Mechanical and Thermal Properties of Pressureless Sintered Silicon Carbide Ceramics with Alumina–Yttria–Calcia

The effect of sintering temperature on the mechanical and thermal properties of SiC ceramics sintered with Al₂O₃–Y₂O₃–CaO without applied pressure was investigated. SiC ceramics containing A₂O₃–Y₂O₃–CaO as sintering additives can be sintered to >97% theoretical density at temperatures between 1750°C and 1900°C without applied pressure. A toughened microstructure, consisting of relatively large elongated grains and relatively small equiaxed grains, has been obtained when sintered at temperatures as low as 1800°C for 2 h in an argon atmosphere without applied pressure. The achievement of toughened microstructures under such mild conditions is the result of the additive composition. The thermal conductivity of the SiC ceramics increased with increasing sintering temperature because of the decrease in the lattice oxygen content of the SiC grains. Typical sintered density, flexural strength, fracture toughness, hardness, and thermal conductivity of the 1850°C‐sintered SiC, which consisted of 62.2% 4H, 35.7% 6H, and 2.1% 3C, were 99.0%, 628 MPa, 5.3 MPa·m^1/2, 29.1 GPa, and 80 W·(m·K)^?1, respectively.     

Zrc ceramics incorporated with different-sized SiC particles

ABSTRACT

Three different SiC powders with average particle sizes of 0.45, 3.5 and 10?µm were used to prepare ZrC-20vol.-% SiC ceramics by hot pressing. The effects of SiC particle size on the densification, microstructure, mechanical properties and thermal properties of ZrC–SiC ceramics were studied. Ceramics prepared from SiC with finer particle sizes exert higher bending strength, hardness and lower thermal conductivity. The ZrC–SiC ceramics with a starting SiC particle size of 3.5?µm has relative high fracture toughness than others. Analysis indicates that SiC grain size and the grain boundaries control the thermal conductivity ZrC–SiC ceramics. Ceramics prepared from SiC with the particle size of 10?µm exhibits the highest thermal conductivity due to the larger grains and less grain boundaries.     

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.     

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.     

Characterization of B4C-SiC ceramic composites prepared by ultra-high pressure sintering

Additive-free boron carbide (B₄C) – silicon carbide (SiC) ceramic composites with different B₄C and β-SiC powders ratio were densified using the high-pressure “anvil-type with hollows” apparatus at 1500 °C under a pressure of 4 GPa for 60 s in air. The effect of starting powders ratio on the composites sintering behavior, relative density, microstructural development, and thermomechanical properties was studied. The sintered samples hardness was found to be in the range from 24 to 31 GPa. The thermal conductivity measurements, conducted in the temperature range from room temperature to 1000 °C, showed that the thermal diffusivity of sintered samples was between 6 and 9.5 mm²/s whereas the thermal conductivity was in the range from 16 to 28 W/(m K). The results of this study show that the high-pressure sintering can be a very effective low-temperature densification method for the obtainment of additive-free B₄C - β-SiC ceramic composites.     

Fabrication and characterization of SPS sintered SiC-based ceramic from Y3Si2C2-coated SiC powders

The Y₃Si₂C₂ coating was in-situ synthesized on the surface of SiC powders to form SiC-Y₃Si₂C₂ core-shell structure by using a molten salt technique. Phase diagram calculations on Si-Y-C ternary phase at different temperatures well illustrated that the Y₃Si₂C₂ phase can be stable with SiC but will be in liquid state at 1560?°C. The liquid Y₃Si₂C₂ explained the enhanced consolidation of SiC ceramics and its disappearance after spark plasma sintering. Such Y₃Si₂C₂ coating could not only effectively improve the sintering, but also their mechanical and thermal properties of resultant ceramics. Typically, at 1700?°C, the bulk SiC ceramic presented a mean grain size of 2.5?um and relative density of 99.5% when the molar ratio of Y to SiC is 1:4 in molten salts; the Young’s modulus, indentation hardness and fracture toughness measured by indentation test were 451.7?GPa, 26.3?GPa and 7.9?M?Pam^1/2, respectively; the thermal conductivity is about 145.9?W/(m?K). Excellent thermal and mechanical properties could be associated with the fine grain size, optimized phase composition and improved grain boundary structure.     

Effect of temperature on the structure and mechanical properties of SiC–TiB2 composite ceramics by solid-phase spark plasma sintering

SiC composite ceramics have good mechanical properties. In this study, the effect of temperature on the microstructure and mechanical properties of SiC–TiB₂ composite ceramics by solid-phase spark plasma sintering (SPS) was investigated. SiC–TiB₂ composite ceramics were prepared by SPS method with graphite powder as sintering additive and kept at 1700 °C, 1750 °C, 1800 °C and 50 MPa for 10min.The experimental results show that the proper TiB₂ addition can obviously increase the mechanical properties of SiC–TiB₂ composite ceramics. Higher sintering temperature results in the aggregation and growth of second-phase TiB₂ grains, which decreases the mechanical properties of SiC–TiB₂ composite ceramics. Good mechanical properties were obtained at 1750 °C, with a density of 97.3%, Vickers hardness of 26.68 GPa, bending strength of 380 MPa and fracture toughness of 5.16 MPa m^1/2.     

High-entropy (HfTaTiNbZr)C and (HfTaTiNbMo)C carbides fabricated through reactive high-energy ball milling and spark plasma sintering

Powders of high-entropy Hf_0.2Ta_0.2Ti_0.2Nb_0.2Zr_0.2C (HEC_Zr) and Hf_0.2Ta_0.2Ti_0.2Nb_0.2Mo_0.2C (HEC_Mo) carbides were fabricated through the reactive high-energy ball milling (R-HEBM) of metal and graphite particles. It was found that 60 min of R-HEBM is adequate to achieve a full conversion of the initial precursors into a FCC solid solution for both compositions. The HEC_Zr powder possesses a unimodal particle size distribution (40% d ≤ 1 μm, 95% d ≤ 10 μm), and the HEC_Mo powder features a bimodal distribution with a slightly larger particle size overall (30% d ≤ 1 μm, 80% d ≤ 10 μm). Bulk high-entropy ceramics with a minor presence of an oxide phase were fabricated through the spark plasma sintering of these high-entropy powders at 2000 °C with a 10 min dwelling time. The HEC_Zr ceramics possess a relative density of up to 94.8%, hardness of 25.7 ± 3.5 GPa, Young's modulus of 473 ± 37 GPa, and thermal conductivity of 5.6 ± 0.1 W/m·K. HEC_Mo ceramics with a relative density of up to 93.8%, hardness of 23.8 ± 2.7 GPa, Young's modulus of 544 ± 48 GPa, and thermal conductivity of 5.9 ± 0.2 W/m·K were also fabricated. A comparison of the properties of the HECs produced in this study and those previously reported is also provided.     

Properties of MgO transparent ceramics prepared at low temperature using high sintering activity MgO powders

Transparent MgO ceramics are successful fabricated via spark plasma sintering at lower temperature using the high sintering activity powders synthesized by precipitated method. The samples were detected by XRD, SEM, TEM, BET, UV-Vis-NIR, microhardness, and so on. The results show that all ceramics prepared at 700°C-900°C are visually transparent and the sample sintered at 860°C for 5 min exhibits the superior transmittance of 60% (800 nm). It is also found that the mechanical and thermal properties of MgO ceramics are all increasing firstly and then decreasing with the increase in the sintering temperature. And the maximum value of hardness, fracture toughness, MSP strength, and Young's modulus of MgO ceramics is 8.25 GPa, 2.01 MPa·m^1/2, 206 MPa, and 286 GPa, respectively. Moreover, the thermal conductivity of MgO ceramics sintered at 860°C can reach 48.4 W/mK at room temperature.     

Effect of carbon content on electrical,thermal, and mechanical properties of porous SiC ceramics with B4C and C additives

The electrical, thermal, and mechanical properties of porous SiC ceramics with B₄C-C additives were investigated as functions of C content and sintering temperature. The electrical resistivity of porous SiC ceramics decreased with increases in C content and sintering temperature. A minimal electrical resistivity of 4.6 × 10^?2 Ω·cm was obtained in porous SiC ceramics with 1 wt% B₄C and 10 wt% C. The thermal conductivity and flexural strength increased with increasing sintering temperature and showed maxima at 4 wt% C addition when sintered at 2000 °C and 2100 °C. The thermal conductivity and flexural strength of porous SiC ceramics can be tuned independently from the porosity by controlling C content and sintering temperature. Typical electrical resistivity, thermal conductivity, and flexural strength of porous SiC ceramics with 1 wt% B₄C-4 wt% C sintered at 2100 °C were 1.3 × 10^?1 Ω·cm, 76.0 W/(m·K), and 110.3 MPa, respectively.     

Effects of initial α-phase content on properties of pressureless solid-state sintered SiC ceramics

α- and β-SiC starting powders of similar particle sizes were used to investigate the effect of initial α-phase content on the electrical, thermal, and mechanical properties of pressureless solid-state sintered (PSS) SiC ceramics with B₄C and C additives. For β-SiC starting powders, a coarse-grained microstructure with elongated platelet grains was formed by the transformation of 3C to 6H and finally to 4H-SiC phase. In contrast, materials prepared from α-SiC powders exhibited a fine-grained microstructure with platelet grains. This study revealed the beneficial effect of α-SiC starting powders in achieving low electrical resistivity and high thermal conductivity in PSS SiC ceramics, which was attributable to their higher sinterability, lower impurity content, and lower 6H to 4H-SiC phase transformation rate compared with β-SiC powders. The electrical resistivity decreased by an order of magnitude and the thermal conductivity increased by 32% with an increase in initial α-phase content from 0 to 100%. The flexural strength increased by approximately 16% with increasing initial α-phase content due to a decreased flaw size with decreasing grain size. However, the fracture toughness and hardness were insensitive to the change in initial α-phase content.     

Combustion synthesis of high-temperature ZrB2-SiC ceramics

The work is dedicated to researching into combustion kinetics and mechanism as well as the stages of the chemical transformations during self-propagating high-temperature synthesis of ZrB₂-SiC based ceramics. Dependences of the combustion temperature and rate on the initial temperature (T₀) have been studied. It has been shown that the stages of the chemical reactions of ZrB₂ diboride and SiC carbide formation do not change within the range of T_0?=?298–700?К. The effective activation energy of the combustion process amounted to 170–270?kJ/mol, from which it has been concluded that chemical interaction through the melt plays a leading role. The stages of the chemical transformations in the combustion wave have been studied by dynamic X-ray diffraction. First, ZrB₂ phase forms from Zr-Si melt saturated with boron, and SiC phase is registered later. The SHS method has successfully been used in order to obtain ZrB₂-SiC composite powders and compact ceramics with a silicon carbide content of 25–75%. The ceramics are characterized by a residual porosity of 1.5%, hardness up to 25?GPa, the elastic modulus of 318?±?21?GPa, elastic recovery of 36% and thermal conductivity of 54.9?W/(m?×?K) at T_room.     

Fabrication of transparent Y2O3 ceramics with record-high thermal shock resistance

Sintering-additive-free fine-grained highly transparent Y₂O₃ ceramics featuring record-high thermal shock resistance were fabricated using commercial powders via vacuum pre-sintering (1375–1550?°C) followed by hot-isostatic pressing (1450?°C). The sample pre-sintered at 1450?°C provides the optimum microstructure for post HIPing, which resulted in a grain size of 0.64?μm. The transmittance, microhardness and fracture toughness of the thus HIPed sample are 80.8% at 1100?nm and 65.5% at 400?nm (1.2?mm thick), 8.0?±?0.02?GPa and 1.00?±?0.06?MPa?m^1/2, respectively. The thermal conductivity increases from 13.1 to 16.5?W/m/K with increasing vacuum pre-sinterin Proc. SPIE-Int. Soc. Opt g temperature from 1450 to 1550?°C. This hybrid sintering method realized high thermal conductivity and high strength simultaneously. Consequently, the thermal shock resistance of the HIPed specimen vacuum pre-sintered at 1450?°C in this work is the highest ever reported to the best of our knowledge, which makes the developed material a promising candidate for high-power laser host and IR dome.     

Effect of ZrB2 content on the densification,microstructure, and mechanical properties of ZrC-SiC ceramics

ZrC ceramics containing 30 vol% SiC-ZrB₂ were produced by high-energy ball milling and reactive hot pressing. The effects of ZrB₂ content on the densification, microstructure, and mechanical properties of ceramics were investigated. Fully dense ceramics were achieved as ZrB₂ content increased to 10 and 15 vol%. The addition of ZrB₂ suppressed grain growth and promoted dispersion of the SiC particles, resulting in fine and homogeneous microstructures. Vickers hardness increased from 23.0 ± 0.5 GPa to 23.9 ± 0.5 GPa and Young’s modulus increased from 430 ± 3 GPa to 455 ± 3 GPa as ZrB₂ content increased from 0 to 15 vol%. The increases were attributed to a combination of the higher relative density of ceramics with higher ZrB₂ content and the higher Young’s modulus and hardness of ZrB₂ compared to ZrC. Indentation fracture toughness increased from 2.6 ± 0.2 MPa⋅m^1/2 to 3.3 ± 0.1 MPa⋅m^1/2 as ZrB₂ content increased from 0 to 15 vol% due to the increase in crack deflection by the uniformly dispersed SiC particles. Compared to binary ZrC-SiC ceramics, ternary ZrC-SiC-ZrB₂ ceramics with finer microstructure and higher relative densities were achieved by the addition of ZrB₂ particles.     

Low‐Temperature Sintering of HfC/SiC Nanocomposites Using HfSi2‐C Additives

HfC/SiC nanocomposites were fabricated via the reactive spark plasma sintering (R‐SPS) of a nano‐HfC powder and HfSi₂‐C sintering additives. The densification temperature decreased to 1750°C as the additive content increased. XRD analysis indicated the formation of pure HfC–(19.3–33.8 vol%) SiC within the sintered composites without residual silicide or oxide phases or secondary nonoxide phases. Ultrafine and homogeneously distributed HfC (470 nm) and SiC (300 nm) grains were obtained in the dense composites using nano‐HfC powder through the high‐energy ball‐milling of the raw powders and R‐SPS. Grain growth was further suppressed by the low‐temperature sintering using R‐SPS. No amorphous phase was identified at the grain boundary. The maximum Vickers hardness, Young's modulus, and fracture toughness values of the HfC/SiC nanocomposites were 22 GPa, 292 GPa, and 2.44 MPa·m^1/2, respectively.     

Densification,microstructure, and mechanical properties of ZrC–SiC ceramics

ZrC–SiC ceramics were fabricated by high-energy ball milling and reactive hot pressing of ZrH₂, carbon black, and varying amounts of SiC. The ceramics were composed of nominally pure ZrC containing 0 to 30 vol% SiC particles. The relative density increased as SiC content increased, from 96.8% for nominally pure ZrC to 99.3% for ZrC-30 vol% SiC. As SiC content increased from 0 to 30 vol%, Young's modulus increased from 404 ± 11 to 420 ± 9 GPa and Vickers hardness increased from 18.5 ± 0.7 to 23.0 ± 0.5 GPa due to a combination of the higher relative density of ceramics with higher SiC content and the higher Young's modulus and hardness of SiC compared to ZrC. Flexure strength was 308 ± 11 MPa for pure ZrC, but increased to 576 ± 49 MPa for a SiC content of 30 vol%. Fracture toughness was 2.3 ± 0.2 MPa·m^1/2 for pure ZrC and increased to about 3.0 ± 0.1 MPa·m^1/2 for compositions containing SiC additions. The combination of high-energy ball milling and reactive hot pressing was able to produce ZrC–SiC ceramics with sub-micron grain sizes and high relative densities with higher strengths than previously reported for similar materials.     

Thermal and Electrical Properties in Plasma-Activation-Sintered Silicon Carbide with Rare-Earth-Oxide Additives

This study investigates the thermal and electrical properties of SiC ceramics with a combination of Y₂O₃ and rare-earth-oxide additions as sintering additives, by comparing four types of SiC starting powders varying in particle size and chemical composition. The powder mixtures were plasma-activation sintered to full densities and then annealed at high temperatures for grain growth. The thermal conductivity and electrical resistivity of the SiC ceramics were measured at room temperature by a laser-flash technique and a current–voltage method, respectively. The results indicate that the thermal conductivity and electrical resistivity of the SiC ceramics are dependent on the chemical composition and particle size of the starting powders. The thermal conductivities observed for all of the annealed materials with a rare-earth La₂O₃ sintering additive were >160 W·(m·K)⁻¹, although low electrical resistivity was observed for all materials, in the range 3.4–450 Ω·cm. High thermal conductivity, up to 242 W·(m·K)⁻¹, was achieved in an annealed material using a commercial 270 nm SiC starting powder.     

Investigation of optical,mechanical, and thermal properties of ZrO2-doped Y2O3 transparent ceramics fabricated by HIP

Highly transparent ZrO₂-doped Y₂O₃ ceramics were successfully synthesized using the hot isostatic pressing (HIP) process. The effects of the ZrO₂ content on the sintering behaviors, optical transmission spectra, Vickers hardness, grain size, size distribution, and Raman spectra were determined. The results indicated that decreased ZrO₂ content could promote increased transmittance, red-shifted infrared cutoff wavelength, increased thermal conductivity, decreased Vickers hardness, and increased lattice ordering. According to the optical transmission spectra, the optimized ZrO₂ content was 0.50 at%, at which point the ceramic exhibited a larger pre-sintering temperature range of 1650–1750 °C and the average grain size of 3.35 µm at 1750 °C. The grain size was significantly decreased at lower pre-sintering temperatures. Furthermore, a moderate Vickers hardness of 8.42 GPa and high thermal conductivity of 10.85 W/m K at room temperature were obtained for the optimized ceramic.     

The thermo-mechanical properties and ferroelastic phase transition of RENbO4 (RE = Y,La, Nd,Sm, Gd,Dy, Yb) ceramics

In this work, RENbO₄ (RE = Y, La, Nd, Sm, Gd, Dy, Yb) ceramics with low density, low Young's modulus, low thermal conductivity, and high thermal expansion have been systematically investigated, the excellent thermo-mechanical properties indicate that RENbO₄ ceramics possess the potential as the new generation of thermal barrier coatings (TBCs) materials. X-ray diffraction and Raman spectroscopy phase structure identification reveal that all dense bulk specimens obtained by high-temperature solid-state reaction belonged to the monoclinic (m) phase with C12/c1 space group. The ferroelastic domains are detected in the specimens, revealing the ferroelastic transformation between tetragonal (t) and monoclinic (m) phases of RENbO₄ ceramics. The Young's modulus and hardness of the RENbO₄ ceramics measured by the NanoBlitz 3D nanoindentation method are discussed in details, and the lower Young's modulus (60-170 GPa) and higher hardness (the maximum value reaches 11.48 GPa) indicating that higher resistance of RENbO₄ ceramics to failure and damage. Lower thermal conductivity (1.42-2.21 W [m k]⁻¹ at 500°C-900°C) and lower density (5.330-7.400 g/cm³) than other typical TBCs materials give RENbO₄ ceramics the unique advantage of being new TBCs materials. Meanwhile, the thermal expansion coefficients of RENbO₄ ceramics reach 9.8-11.6 × 10⁻⁶ k⁻¹ and are comparable or higher than other typical TBCs materials. According to the first-order derivative of the thermal expansion rate, the temperature of the ferroelastic transformation of RENbO₄ ceramics can be observed.     

Synthesis,densification, microstructure,and mechanical properties of samarium hexaboride ceramic

Samarium hexaboride (SmB₆) powders were synthesized by boro/carbothermal reduction of Sm₂O₃ with B₄C. Nominally pure SmB₆ powder had a mean particle size of about 400 nm and an oxygen content of 0.12 wt%. SmBO₃ formed as an intermediate phase during the synthesis. The synthesized powder was hot pressed at 1950°C to produce SmB₆ ceramics with relative densities >99.6% and a mean grain size of 4.4 μm. Vickers’ hardness was 20.1 ± 0.7 GPa. Young's modulus measured by bending and ultrasonic methods was 271 and 244 GPa, respectively. The flexure strength was 253 ± 79 MPa and fracture toughness was 2.1 ± 0.1 MPa m^1/2. These are the first reported results of the microstructure and bulk mechanical behavior of SmB₆ ceramics.