Processing and properties of porous SiC ceramics prepared by yttrium aluminum garnet infiltration

Oxide bonded porous SiC ceramics were synthesized by infiltrating a liquid precursor of yttrium aluminum garnet into porous powder compact of SiC followed by sintering at 1300‐1500°C in air. Infiltration rate was estimated using weight gain by the liquid precursor sol into porous SiC powder compact as a function of time and was explained by Darcy's and Ficks's laws. The effects of SiC particle sizes and sintering temperatures on the formation of bonding phases, microstructure, SiC oxidation degree, flexural strength, porosity, and pore size distribution of porous SiC ceramics were studied. Various crystalline oxide phases were detected by XRD analysis. Depending on the starting SiC powder sizes and sintering temperatures, the porosity of the final ceramics varied nearly in the range of ~29‐41 vol. % with the variation of average pore diameter between ~5 and 30 μm. Flexural strength varied from 41 to 8 MPa depending on porosity. The effect of corrosion on oxide bond phases was investigated in strong acidic and basic medium at 90°C. The ceramics showed better corrosion resistance in acidic medium compared to basic medium. In basic medium, significant reduction in flexural strength (~42%) was arisen.     

Permeability and corrosion resistance of porous SiOC-bonded SiC ceramics prepared by the preceramic polymer

Porous SiC ceramics have been used in high temperature flue gas filtration fields because of their excellent properties such as high strength, high temperature resistance, corrosion resistance, and long service time. This work reports the porous SiOC-bonded SiC ceramics prepared at low temperature. The properties of porous SiC ceramics were first investigated with silicone resin content from 10 to 25 wt%, and then the effects of different pore-forming agent contents on the behaviors of porous SiC ceramics were discussed by adjusting poly (methyl methacrylate) PMMA microbeads from 5 to 20 wt%. The prepared porous SiC ceramics showed apparent porosity from 17.3% to 57.7%, compressive strength from 6 to 216 MPa, and Darcy permeability k₁ ranging from 7.02 × 10⁻¹⁴ to 1.45 × 10⁻¹² m². The corrosion behavior of porous SiC ceramics was investigated in acidic and alkaline media. The porous SiC ceramics showed better corrosion resistance in acidic solutions.     

Effects of SiC whisker addition on mechanical,thermal, and permeability properties of porous silica-bonded SiC ceramics

The effects of SiC whisker addition into nano-SiC powder-carbon black template mixture on flexural strength, thermal conductivity, and specific flow rate of porous silica-bonded SiC ceramics were investigated. The flexural strength of 1200°C-sintered porous silica-bonded SiC ceramics increased from 9.5 MPa to 12.8 MPa with the addition of 33 wt% SiC whisker because the SiC whiskers acted as a reinforcement in porous silica-bonded SiC ceramics. The thermal conductivity of 1200°C-sintered porous silica-bonded SiC ceramics monotonically increased from 0.360 Wm^–1K^–1 to 1.415 Wm^–1K^–1 as the SiC whisker content increased from 0 to 100 wt% because of the easy heat conduction path provided by SiC whiskers with a high aspect ratio. The specific flow rate of 1200°C-sintered porous SiC ceramics increased by two orders of magnitude as the SiC whisker content increased from 0 to 100 wt%. These results were primarily attributed to an increase in pore size from 125 nm to 565 nm and secondarily an increase in porosity from 49.9% to 63.6%. In summary, the addition of 33 wt% SiC whisker increased the flexural strength, thermal conductivity, and specific flow rate of porous silica-bonded SiC ceramics by 35%, 133%, and 266%, respectively.     

SiC多孔陶瓷制备方法研究进展

碳化硅(SiC)多孔陶瓷作为一种重要的结构材料,具有高熔点、高强度、比表面积大、体积密度小、热膨胀系数小以及良好的化学稳定性等优点,被广泛应用于催化剂载体、气/液过滤装置、生物医学材料、保温材料和耐火材料等领域。SiC多孔陶瓷的微观结构、性能及服役寿命等均受其制备方法的影响,因此综述了近年来国内外在SiC多孔陶瓷制备方法方面的研究进展,总结了物理成孔法(包括颗粒堆积法、冷冻干燥法及3D打印法等)和化学成孔法(包括添加造孔剂法、有机泡沫浸渍法与生物模板法等)制备SiC多孔陶瓷的优缺点,并对其发展方向和重点进行了展望。     

High-temperature flexural strength of SiC ceramics prepared by additive manufacturing

Silicon carbide (SiC) ceramics, as a kind of candidate material for aero-engine, its high-temperature performance is a critical factor to determine its applicability. This investigation focuses on studying the high-temperature properties of SiC ceramics fabricated by using additive manufacturing technology. In this paper, SiC ceramics were prepared by combining selective laser sintering (SLS) with precursor infiltration and pyrolysis (PIP) technique. The microstructure, phase evolution, and failure mechanism after high-temperature tests were explored. SiC ceramic samples tested at room temperature (RT), 800°C, 1200°C, 1400°C, and 1600°C demonstrated bending strengths of 220.0, 226.1, 234.9, 215.5, and 203.7 MPa, respectively. The RT strength of this material can be maintained at 1400°C, but it decreased at 1600°C. The strength retention at 1400°C and 1600°C were 98% and 92%, respectively. The results indicate that the mechanical properties of SiC ceramics prepared using this method have excellent stability. As the temperature increases, the bending strength of the specimens increased slightly and reached the peak value at 1200°C, and dropped to 203.7 MPa at 1600°C. Such an evolution could be mainly due to the crack healing, and the softening of the glassy phase.     

Microstructure and properties of porous SiC ceramics by LPCVI technique regulation

A new gradient pore structure in porous SiC ceramics was fabricated by low pressure chemical vapor infiltration (LPCVI). Effects of deposition duration on the mechanical properties and permeability of porous SiC ceramics were investigated. Results demonstrated that pore diameter and shapes decreased from the surface to the interior along with LPCVI duration. Porous SiC ceramics with deposition duration of 160 h exhibited flexural strength of 48.05 MPa and fracture toughness of 1.30 MPa m^1/2, where 221% and 189% improvements were obtained compared to porous SiC ceramics without LPCVI, due to CVI-SiC layer strengthening effect. Additionally, at the same gas velocity, pressure drop increase rate was faster due to apparent porosity and pore size change.     

Studies on processing of layered oxide-bonded porous sic ceramic filter materials

Oxide-bonded porous SiC ceramic filter supports were prepared using SiC powder (d₅₀ = 212 µm), Al₂O₃, and clay as bond forming additives and graphite as pore former following reaction bonding of powder compacts at 1400°C in air. Reaction bonding characteristics, phase composition, porosity, pore size, mechanical strength, and microstructure of porous SiC ceramic supports were investigated. Mullite bond phase formation kinetics was studied following the Johnson–Mehl–Avrami–Kolmogorov (JMAK) model using non-isothermal differential thermal analysis (DTA) data. Compared to porous SiC ceramic filter supports having no needle-like mullite bond phase, materials processed by the mullite bonding technique exhibited higher average strength (22.1%) and elastic modulus (5.4%) at a similar porosity level of ~38%, with upper and lower bounds of their strength, modulus, and porosity being 39.1 MPa, 40.2 GPa, and 36.3% and 34.2 MPa, 31.3 GPa, and 33.0%, respectively. Spray coating method was applied for preparation of oxidation-bonded SiC filtration layer having thickness of ~150 µm and pore size of ~5–20 µm over the porous SiC support compacts using aqueous slurry made of fine SiC powder (d₅₀ = 15 µm) followed by sintering. The layered ceramics thus prepared are potential materials for gas filter applications.     

Anisotropic compressive properties of porous CNT/SiC composites produced by direct matrix infiltration of CNT aerogel

Carbon nanotube‐reinforced silicon carbide composites (CNT/SiC) produced by direct infiltration of matrix into a porous CNT arrays have been demonstrated to possess a unique microstructure and excellent micro‐mechanical properties. However, the thickness of the array preforms is usually very small, typically less than 2 mm. Therefore, fabrication of macroscopic CNT/SiC composites by chemical vapor infiltration (CVI) process requires that the nanoscale fillers could form macroscopic architectures with an open pore network. Here, this study reports an experimental strategy for the fabrication of SiC matrix composites reinforced by CNT based on an ice‐segregation‐induced self‐assembly (ISISA) technique. Macroscopic CNT aerogel with well‐defined macroporous network was produced by ISISA technique and was subsequently infiltrated by SiC in a CVI reactor. After five CVI cycles, the porosity of as‐fabricated composites was 11.6±0.3% and the machined specimens exhibited lamellar structure with parallel lamellaes intersected at discrete angles. By observed, there are in fact five different representative anisotropic macrostructures, the compressive strengths of these five different loading modes with respect to lamella orientation were 933±55, 619±34, 200±45, 199±21, and 297±41 MPa, respectively, and the failure mechanisms were attributed to the anisotropic nature of the macrostructures. Energy dissipation toughening mechanism at the nanoscale such as CNT pull‐out was observed and the phase composition of the fabricated materials included β‐SiC, CNT, and SiO₂.     

Microstructure and gas permeation performance of porous silicon nitride ceramics with unidirectionally aligned channels

Porous Si₃N₄ ceramics with unidirectionally aligned channels were prepared via freezing ceramics suspension with distinct solid contents under different freezing temperatures. The samples obtained using lower solid content in ceramic suspension at higher freezing temperature exhibit larger Darcian and non-Darcian constants due to their higher open porosity, larger pore size and lower tortuosity. Moreover the investigation on individual contributions of viscous energy losses and inertial energy losses on the total pressure drop during permeation process indicates that with decreasing the solid content or the freezing temperature the viscous energy losses increase but the inertial energy losses decrease for samples owing to the differences in their pore structures. It is worth mentioning that porous Si₃N₄ ceramics with unidirectionally aligned channels exhibit larger Darcian and non-Darcian constants than those with similar pore size distributions and open porosity owing to their lower tortuosity, thus rendering them appropriate for filters and membrane supports.     

Electrical,thermal, and mechanical properties of porous silicon carbide ceramics with a boron carbide additive

The effects of the boron carbide (B₄C) content and sintering atmosphere on the electrical, thermal, and mechanical properties of porous silicon carbide (SiC) ceramics were investigated in the porosity range of 58.3%–70.3%. The electrical resistivities of the nitrogen-sintered porous SiC ceramics (∼10^–1 Ω·cm) were two orders of magnitude lower than those of argon-sintered porous SiC ceramics (∼10¹ Ω·cm). Both the thermal conductivities (3.3–19.8 W·m^–1·K^–1) and flexural strengths (8.1–32.9 MPa) of the argon- and nitrogen-sintered porous SiC ceramics increased as the B₄C content increased, owing to the decreased porosity and increased necking area between SiC grains. The electrical resistivity of the porous SiC ceramics was primarily controlled by the sintering atmosphere owing to the N-doping from the nitrogen atmosphere, and secondarily by the B₄C content, owing to the B-doping from the B₄C. In contrast, the thermal conductivity and flexural strength were dependent on both the porosity and necking area, as influenced by both the sintering atmosphere and B₄C content. These results suggest that it is possible to decouple the electrical resistivity from the thermal conductivity by judicious selection of the B₄C content and sintering atmosphere.     

Electrically conductive SiC ceramics processed by pressureless sintering

Polycrystalline SiC ceramics with 10 vol% Y₂O₃-AlN additives were sintered without any applied pressure at temperatures of 1900-2050°C in nitrogen. The electrical resistivity of the resulting SiC ceramics decreased from 6.5 × 10¹ to 1.9 × 10⁻² Ω·cm as the sintering temperature increased from 1900 to 2050°C. The average grain size increased from 0.68 to 2.34 μm with increase in sintering temperature. A decrease in the electrical resistivity with increasing sintering temperature was attributed to the grain-growth-induced N-doping in the SiC grains, which is supported by the enhanced carrier density. The electrical conductivity of the SiC ceramic sintered at 2050°C was ~53 Ω⁻¹·cm⁻¹ at room temperature. This ceramic achieved the highest electrical conductivity among pressureless liquid-phase sintered SiC ceramics.     

Extrusion of highly porous silicon nitride ceramics with bimodal pore structure and improved gas permeability

Highly porous Si₃N₄ ceramics with bimodal pore structure were prepared by the extrusion processing with petroleum coke of 30 μm as pore‐maker. The microstructure, mechanical strength, and gas permeability were investigated. The microstructure with petroleum coke contained not only numerous fine pores by interlocking the high aspect ratio β‐Si₃N₄ grains, but also some large pores of 15‐25 μm left by the burnout of petroleum coke. The resultant samples obtained an improved gas permeability of 1.2 × 10^?12 m², which is approximately two times that of samples without petroleum coke addition. Furthermore, the mechanical strength is still superior even at a porosity of 67% in comparison with the other porous ceramics used in the current diesel particulate filter.     

生物SiC多孔陶瓷的研究进展

介绍了生物SiC多孔陶瓷的研究现状,并对生物碳模板的分类、制备方法进行了详尽的叙述,同时对生物SiC多孔陶瓷的各项性能进行了综述,最后对生物SiC多孔陶瓷的发展趋势作了总结。     

CF/SiC增强摩阻材料性能研究

采用模压法制备了碳纤维(CF)/碳化硅(SiC)增强摩阻材料,通过摩擦试验研究了CF和SiC质量分数及CF长度对材料摩擦磨损特性的影响。结果表明:随着SiC质量分数的增加,摩擦系数和磨损率都有明显提高,这是由于硬质颗粒的犁沟作用;当CF质量分数<10%时,CF质量分数和长度对摩擦磨损性能影响明显,这归因于CF本身具有良好的自润滑性能以及抗犁削作用。     

Lattice-structured SiC ceramics obtained via 3D printing,gel casting,and gaseous silicon infiltration sintering

In view of technical difficulties in preparing ceramics with complex shapes, gel casting combined with 3D printing was here adopted to prepare silicon carbide ceramic green body, and gaseous silicon infiltration sintering was used to prepare 3D lattice-structured ceramics. The preparation of the slurry, gel curing, and ceramic molding was investigated. Results demonstrate that the ratio of components affects the fluidity and stability of slurry. However, when volume fraction of the solid phase of the slurry reaches 56%, the viscosity of slurry is only 300 mPa s, and drying shrinkage rate of green body is 6.6%; these characteristics make slurry suitable for 3D complex model injection molding. Furthermore, both the temperature and the initiator affect gel curing speed. As the temperature and initiator content increase, the induction and gel time are rapidly shortened. When demolding at 300 °C and when gaseous silicon infiltration sintering is carried out at 1550 °C, a 3D lattice-structured ceramic with relative density of 87% and average compressive strength of 433 MPa can be obtained.     

堇青石多孔陶瓷制备及其性能优化研究进展

堇青石多孔陶瓷因具有高的孔隙率,优异的力学强度和良好的抗热震性能而被用作汽车尾气催化剂的载体材料.为此,综述了堇青石多孔陶瓷的制备方法和掺杂元素与其性能(孔结构、抗热震性和力学强度等)的相关性,同时指出了堇青石多孔陶瓷在制备过程中存在的问题,并展望了作为汽车尾气催化剂载体的堇青石多孔陶瓷未来的发展方向.     

氟化铝添加量对碳化硅/莫来石复合多孔陶瓷性能的影响

本文以碳化硅(SiC)、气相SiO2、纳米Al2O3和AlF3·H2O为原料,制备出了碳化硅/莫来石复合多孔陶瓷,主要研究了AlFa·H2O添加量、烧结温度对多孔陶瓷抗弯强度、气孔率、孔径分布等性能的影响.用SEM、XRD研究了多孔陶瓷的微观形貌和物相组成.结果表明:AlF3·H2O对莫来石的生成有明显的促进作用,1300℃时,添加AlF3·H2O的样品中检测到莫来石相,多孔陶瓷气孔率随AlF3·H2O加入量增加而升高,而抗弯强度随其增高而先增加后减小,AlF3·H2O添加量为4wt％时,多孔陶瓷气孔率为42.8％,抗弯强度为31.1 MPa.     

Ultra-high creep resistant SiC ceramics prepared by rapid hot pressing

The high-temperature compression creep of additive-free β/α silicon carbide ceramics fabricated by rapid hot pressing (RHP) was investigated. The creep tests were accomplished in vacuum at temperature range 1500 °C–1750 °C and compressive loads of 200 MPa to 400 MPa. Under investigated condition the RHP ceramics possessed the lowest creep rate reported in the literature. The observed strain rates changed from 2.5 × 10^?9 s^?1 at 1500 °C and a lowest load of 275 MPa to 1.05 × 10^?7 s^?1 at 1750 °C and a highest load of 400 MPa. The average creep activation energy and the stress exponent remain essentially constant along the whole range of investigated parameters and were 315 ± 20 kJ?mol^?1, and 2.22 ± 0.17, respectively. The suggested creep mechanism involves GB sliding accommodated by GB diffusion and β?α SiC phase transformation.     

Intrinsic microstructures of silica-bonded porous nano-SiC ceramics

Silica-bonded porous SiC ceramics were fabricated using nano-β-SiC powder-carbon black template compacts by sintering in air at 600°C-1200°C. The intrinsic microstructures of the porous ceramics were characterized by high-resolution transmission electron microscopy, which led to the following observations: (a) a core (SiC)-shell (SiO₂) structure was formed, owing to the partial oxidation of nano-SiC particles during sintering; (b) a low-temperature (800°C) β-to-α polytypic phase transformation was observed, owing to the oxidation-induced residual thermal stresses; and (c) non-graphitic carbons were precipitated inside the SiC core, owing to the segregation of C atoms emitted at the strained SiC-SiO₂ interface.