高温处理对渗硅碳化硅性能的影响

研究了全碳粉反应渗硅碳化硅（PCRBSC）材料在1700℃高温氩气氛中4h的处理,研究结果表明,RCPBSC材料的结构对高温处理后的强度有很大的影响,特别是游离硅sfi,游离碳fc的含量明显影响高温处理后PCRBSC材料的抗折强度。     

高温处理对渗硅碳化硅性能的影响

研究了全碳粉反应渗硅碳化硅（ＰＣＲＢＳＣ）材料在１７００℃高温氩气氛中４ｈ的处理,研究结果表明：ＰＣＲＢＳＣ材料的结构对高温处理后的强度有很大的影响,特别是游离硅ｆｓｉ、游离碳ｆｃ的含量明显影响高温处理后ＰＣＲＢＳＣ材料的抗折强度。     

渗硅碳化硅材料结构与性能关系的研究

采用低廉石油焦碳分为原料制造全碳粉生坯，通过有机添加剂来调配生坯中碳的比例，以控制烧结体中游离硅（fsi）、游离碳（fC）含量（其中fs,fc为烧结中未反应的硅和碳），研究了全碳粉反应硅碳化硅（PCRSC）材料的结构与力学性能的关系，分析了渗硅碳化硅材料中游离硅、游了碳含量对抗弯强度的影响。结果表明：渗硅碳化硅材料中随游离硅含量的增加，其抗弯速度下降，并且二者呈直线关系，符合线性复合规则，另一方面，游离碳含量较高的渗硅碳化硅材料，尽管游离硅含量低，但其抗弯强度低于等量或较多游了硅含量的渗硅碳化硅材料的抗弯强度。     

渗硅碳化硅材料的高温氧化

研究了全碳粉反应渗硅碳化硅(PCRBSC)材料,在1300℃静态空气中的高温氧化行为.研究结果表明:PCRBSC材料的氧化过程遵循直线-抛物线规律,其结构对高温氧化有很大的影响,特别是游离硅fsi和游离碳fc的含量对氧化影响更大,fsi含量高的PCRBSC材料单位面积氧化增重(Δm/s)明显,fc含量高的PCRBSC材料氧化后表现为先减重后增重,氧化层断口经扫描电镜观察有明显的气孔存在.     

硅灰对钢纤维混凝土耐久性能的影响研究

为提高钢纤维混凝土耐久性能,采用复掺的方式,选择高品质的硅灰掺入到钢纤维的混凝土结构中。在保证基准配合比相同的情况下,通过不同的硅灰与钢纤维配合比,探讨硅灰对钢纤维混凝土耐久性能的影响。通过实验结果表明,随着硅灰掺入钢纤维混凝土量的增加,混凝土的抗折强度、抗压强度和劈裂强度、抗冻性能都明显提高,并在12%硅灰+1.2%钢纤维时达到最大。     

渗硅碳化硅材料的研究

本文通过调整生坯结构,研究了全碳粉渗硅碳化硅（PCRBSC0的显微结构及力学性能。实验结果表明：生坯结构影响烧结体显微结构,同时显微结构、游离硅含量影响材料力学性能,渗硅碳化硅（PCRBSC0材料中随游离硅含量的增加,其抗折强度下降,并且二者呈直线关系,符合线性复合规则：P＝∑i=1^nPiVi。     

影响碳化硅和碳化硼原料纯度的碳定量分析

开发了湿式氧化分解和电量测定法,该分析法不受含有的杂质的影响,可以定量分析碳化硅原料和碳化硼原料中的游离碳量,精确地求出碳化硅的纯度.     

结合剂对碳化硅浇注料碳化后性能的影响

硅溶胶结合体系可以显著提高碳化硅基浇注料碳化后的热态强度。本试验利用原位反应的机理,在一定粒度级配的碳化硅颗粒中加入硅粉、硅微粉和不同的结合剂为原料,振动成型,然后经过1450℃(3h)埋炭热处理。初步研究了不同品质的结合剂(硅溶胶、铝酸钙水泥)对碳化硅基浇注料碳化后的性能,尤其是热态强度的影响。结果表明:加入少量的炭黑有助于硅溶胶结合碳化硅浇注料的高温抗折强度和热震稳定性的提高,但加入少量的炭黑对碳化反应没有明显的影响。     

熔融渗硅对石墨材料微观结构及性能的影响

选用四种不同孔隙结构的石墨进行熔融渗硅(简称熔渗)反应,采用扫描电镜、X-射线衍射、压汞、CT等方法表征了熔渗前后材料的微观形貌、物相及孔隙结构。结果表明,熔渗后的材料由石墨、硅及碳化硅三种物相组成,且硅及碳化硅的分布与石墨孔隙结构相关。熔渗后样品孔隙率均<1%,体积密度提高21.08%~35.94%。熔渗后材料强度及模量均有明显提高,强度是原石墨样品的1.7~6.2倍,模量是原石墨样品的2.4~7倍,提高幅度与石墨孔隙结构及晶粒尺寸相关。理论计算结果表明,石墨样品熔渗过程主要受扩散-反应控制。     

碳化硅/堇青石复相多孔陶瓷的制备及性能研究

采用碳化硅、烧高岭土、氢氧化铝、滑石为主要原料,石墨为造孔剂制备了碳化硅/堇青石复相多孔陶瓷.研究了烧结温度和烧结助剂二氧化铈对碳化硅/堇青石复相多孔陶瓷气孔率和强度的影响,并分别用XRD和SEM分析晶相组成和断面显微结构表明:制备出的SiC多孔陶瓷的主相是SiC,结合相是堇青石与方石英,多孔陶瓷具有相互连通的开孔结构;在1350℃烧结,并保温3h,当造孔剂含量为15％时,碳化硅/堇青石复合多孔陶瓷性能最佳,其气孔率31.80％,相应的弯曲强度为63.74 MPa.在1200℃下,添加不同含量的CeO2,对烧结样品的相组成有影响,能够降低生成堇青石的温度,在CeO2含量为3％的样品中,堇青石的峰最明显,但是过量的氧化铈会抑制了堇青石的生成;随着CeO2加入量的增加,其气孔率和弯曲强度也会随之变化,1200℃下,在CeO2加入量为4％时其弯曲强度最优.但随着CeO2的含量的增加,其气孔率逐渐下降.     

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.     

Strength of Nicalon Silicon Carbide Fibers Exposed to High-Temperature Gaseous Environments

The effects of exposures to high-temperature gaseous atmospheres on the strength of Nicalon SiC fibers were investigated. The exposure conditions were as follows: (1) H₂ with various P _H2O for 10 h at 1000° and 1200°C, and (2) air for 2 to 100 h at 800° to 1400°C. Individual fibers were tested in tension following each exposure. The strengths of the fibers were strongly influenced by the exposure atmosphere and temperature, but less affected by time at temperature. When exposed in air, a SiO₂ layer was formed on the surface, minimizing the degradation of strength. However, this beneficial effect was negated under conditions in which the SiO₂ layer became too thick. The most severe degradation resulted from exposure to a reducing atmosphere, presumably due to the reduction of SiO₂ inherent in the fibers.     

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.     

预氧化处理对反应烧结碳化硅微观结构和弯曲强度的影响

本文提出了一种简单有效的预氧化处理方法,用来强化反应烧结碳化硅(RBSC),研究了800~1 300 ℃预氧化处理对其微观结构和力学性能的影响,探究了含不同尺寸压痕裂纹的材料在氧化前后残余弯曲强度的变化规律。结果表明,随着氧化温度的升高,RBSC的室温强度和Weibull模数均存在先下降后上升,然后再下降的趋势,主要原因是不同温度氧化后的RBSC表面形貌不同。在1 200 ℃下预氧化2 h,RBSC的弯曲强度和Weibull模数都明显变大,强度提升了19.9%,Weibull模数由7.3提升到11.8。然而,800 ℃低温氧化不完全和1 300 ℃高温氧化反应过于强烈均会导致弯曲强度和Weibull模数下降。在最优氧化条件(1 200 ℃氧化2 h)下,含压痕裂纹(载荷20 N)的RBSC试样的残余弯曲强度在氧化后由201.1 MPa提高到324.2 MPa,强化机理是高温氧化生成的SiO₂能够消除材料表面缺陷和微裂纹。     

Oxidation of Silicon and Silicon Carbide in Ozone-Containing Atmospheres at 973 K

The oxidation behavior of a silicon wafer, chemically vapor-deposited SiC, and single-crystal SiC was investigated in an oxygen—2%–7% ozone gas mixture at 973 K. The thickness of the oxide film that formed during oxidation was measured by ellipsometry. The oxidation rates in the ozone-containing atmosphere were much higher than those in a pure oxygen atmosphere. The parabolic oxidation kinetics were observed for both silicon and SiC. The parabolic rate constants varied linearly with the ozone-gas partial pressure. Inward diffusion of atomic oxygen formed by the dissociation of ozone gas through the SiO₂ film apparently was the rate-controlling process.     

Tensile Rupture Strength and Fracture Defects of Sintered Silicon Carbide

The tensile strength distribution of sintered silicon carbide was measured at room temperature and 1300°C in air and fracture defects were characterized. The measured strength was compared with strength obtained from flaw characteristics and fracture toughness assuming a peripherally cracked spherical void model.     

反应烧结碳化硅研究进展

对有关反应结合碳化硅(RBSC)材料的研究进展作了综述,并对存在的问题和今后可能的发展方向提出了自己的见解,包括:进一步提高性能;降低游离硅含量,提高使用温度;提高材料的可靠性和稳定性;低成本化.     

Conversion of Oak to Cellular Silicon Carbide Ceramic by Gas-Phase Reaction with Silicon Monoxide

Oak has been converted to a porous biocarbon template by annealing in an inert atmosphere above 800°C. Subsequent infiltration with gaseous SiO at 1550–1600°C under flowing argon of atmospheric pressure finally resulted in the formation of a porous, cellular β-SiC ceramic. The conversion retains the biomorphic cellular morphology of oak tissue. While pores in the cell walls with a diameter less than ∼1 μm vanished, two distinct pore channel maxima representing tracheidal cells and large vessels remained in the SiC ceramic. Depending on the cellular morphology of different kinds of wood, e.g., strut thickness and pore size distribution, gas-phase conversion to single-phase β-SiC can be used to manufacture cellular ceramics with a wide range of pore channel diameters.