化学气相渗透法制备2维和2.5维C/SiC复合材料及其拉伸性能

采用化学气相渗透法制备了2维和2.5维碳纤维增强碳化硅(carbon-fiber-reinforced silicon carbide,C/SiC)复合材料,沿经纱(纵向)和纬纱(横向) 2个方向对2种复合材料进行了室温拉伸性能测试,并从预制体结构和原始缺陷分布的角度对比分析了两者力学性能之间的差异.结果表明:两种C/SiC复合材料均表现出明显的非线性力学行为,在经纱方向和纬纱方向上,2维C/SiC复合材料力学性能表现为各向同性,而2.5维C/SiC复合材料力学性能则表现出明显的各向异性:经纱方向上2.5维C/SiC复合材料的拉伸强度和拉伸模量(326 MPa,153 GPa)均高于2维C/SiC复合材料的(245 MPa,96 GPa),纬纱方向上的(145 MPa,62 GPa)均低于2维C/SiC复合材料的(239 MPa,90 GPa).两种复合材料的拉伸断裂行为均表现为典型的韧性断裂,并伴有大量的纤维拔出.两种复合材料中纱线断裂均呈现出多级台阶式断裂方式,但其断裂位置并不相同.2.5维C/SiC复合材料中由于经纱路径近似于正弦波,弯曲程度较大,在纱线交叉点处造成明显的应力集中,因此经纱多在纱线交叉点处断裂;而纬纱由于其路径近乎直线,应力集中现象不明显,因此纬纱断裂位置呈随机分布.2维C/SiC复合材料中经纱和纬纱由于其路径类似于2.5维C/SiC复合材料中的经纱,因此其断裂位置也多在纱线交叉点处.微观结构观察表明不同的编织结构是造成两种复合材料在不同方向上力学性能差异的主要原因.     

碳纤维增强碳化硅陶瓷基复合材料的研究进展及应用

碳纤维增强碳化硅陶瓷基复合材料具有密度低、高强度、高韧性和耐高温等综合性能,已得到世界各国高度重视.本文综述了碳纤维的研究进展,C_f/SiC复合材料的制备方法,并分析了各种制备方法的优缺点.概述了C_f/SiC复合材料作为高温热结构材料和制动材料的应用状况.最后,指出了有待解决的问题和今后的主要研究方向.     

基于核应用下碳化硅陶瓷及其复合材料的连接研究进展

SiC陶瓷及其复合材料凭借其自身固有的核辐射下的稳定性而有望成为新一代核裂变以及未来核聚变反应堆中重要的结构材料.能否满足核应用环境下各种苛刻条件而实现完美连接是其能够得到最终应用的关键.本文综述了目前国际上基于核应用上SiC陶瓷及其复合材料的几种连接工艺的发展情况.     

C/SiC复合材料在超高温燃烧室环境下的烧蚀行为EI北大核心CSCD

针对化学气相渗透法制备的C/SiC复合材料燃烧室,采用发动机燃烧风洞,研究了其在超高温燃气环境下的氧化烧蚀行为,分析了C/SiC复合材料燃烧室内各个区域的烧蚀形貌特征。结果表明:SiC在不同区域表现出不同的烧蚀行为,包括主被动氧化、层流冲刷、湍流冲刷等,这些烧蚀及其耦合作用使得SiC基体被侵蚀以及碳纤维被氧化,最终导致C/SiC复合材料在燃烧时失效。C/SiC复合材料是一种重要的超高温热防护材料,了解在服役环境下这种材料的失效机理是其应用和优化的基础。     

SiC陶瓷及其复合材料连接的研究进展

SiC陶瓷及其复合材料（SiCf／SiC、Cf／SiC）由于具有优良的高温强度、耐磨和抗腐蚀的性能而被广泛关注，而SiC陶瓷及其复合材料的连接是获得这一性能的关键技术之一。综述了SiC陶瓷及其复合材料连接的一般方法和连接技术，同时指出了连接技术的发展趋势。     

C/SiC复合材料在超高温燃烧室环境下的烧蚀行为

针对化学气相渗透法制备的C/SiC复合材料燃烧室,采用发动机燃烧风洞,研究了其在超高温燃气环境下的氧化烧蚀行为,分析了C/SiC复合材料燃烧室内各个区域的烧蚀形貌特征。结果表明:SiC在不同区域表现出不同的烧蚀行为,包括主被动氧化、层流冲刷、湍流冲刷等,这些烧蚀及其耦合作用使得SiC基体被侵蚀以及碳纤维被氧化,最终导致C/SiC复合材料在燃烧时失效。C/SiC复合材料是一种重要的超高温热防护材料,了解在服役环境下这种材料的失效机理是其应用和优化的基础。     

空间望远镜用C/SiC镜面研制综述

综述了空间望远镜的主镜用高强度、高表面精度、低热膨胀系数的低温（约4K）用镜面的制备和检测过程.日本将Φ710mm的高强度反应烧结SiC材料已用于红外望远镜镜面.在短切炭纤维增强C/C复合材料毛坯的基础上进行液相硅渗透（LSI）而制备的C/SiC复合材料在光学镜面方面具有更大的优势.通过提高C/C复合材料毛坯中沥青基炭纤维体积分数及控制硅化速度,可有效地提高LSI-C/SiC复合材料的机械性能和表面光学精度;通过不同规格的炭纤维的混杂化,可使C/SiC复合材料热膨胀系数的各向异性降低至小于4％的差异.SiC、Si-SiC浆料涂层处理可有效地提高表面精度至2 nm rms的极高要求.     

硅树脂高温转化陶瓷结合层连接陶瓷材料

由硅树脂作为先驱体,在高温(800～1400℃)转化陶瓷结合层对石墨、SiC陶瓷及3D(dimension)-Cf(carbon fiber)／SiC复合材料进行了连接实验,着重探讨了硅树脂固化裂解过程、裂解温度、保温时问及升温速率对连接性能的影响。研究表明;硅树脂的交联固化主要是通过消耗Si-OH来完成。对于石墨、SiC的连接,1200℃是较佳的处理温度,而对于Cf／SiC则最佳的处理温度为1400℃。随着保温时间由1h延长到5h,SiC陶瓷连接强度得到提高,但对复合材料的连接不利。低升温速率(2℃／min)时的连接强度比10℃/min时的高很多。     

C/C复合材料与金属材料的热压连接

C／C复合材料作为一种新型的热结构材料,其与传统金属材料的连接越来越具有非常重要的实际意义。本文着重分析了C／C复合材料与金属材料在热压连接过程中存在的关键问题,并概括介绍了C／C复合材料与金属热压连接的连接方法。     

原位生长SiC纳米纤维及其对C/C-ZrC复合材料耐烧蚀性能的影响

采用化学气相反应法在C/C复合材料上原位生长SiC纳米纤维,然后通过高温熔渗反应制备C/C-SiC-ZrC复合材料。通过XRD、SEM、等离子体烧蚀设备分别对其结构、形貌和耐烧蚀性能等进行分析研究。结果表明:C/C复合材料表面生长的SiC纳米纤维直径介于100 nm与1μm之间,最佳反应温度在1 500℃左右。等离子体枪烧蚀30 s后,C/C-ZrC复合材料的质量烧蚀率和线烧蚀率分别为-0.32 mg/s和2.57μm/s;而C/C-SiC-ZrC复合材料的质量烧蚀率和线烧蚀率分别为-0.24 mg/s和1.66μm/s,生长了SiC纳米纤维的C/C-ZrC复合材料展示了更优异的耐烧蚀性能。     

Modelling shear behaviors of 2D C/SiC z-pinned joint prepared by chemical vapor infiltration

Progressive failure model is developed to investigate shear behaviors of 2D C/SiC z-pinned joint prepared by chemical vapor infiltration (CVI). It includes progressive failure model of 2D C/SiC composites and cohesive model of faying plane, in order to describe joint nonlinear shear behaviors and z-pin shear-off failure mode, respectively. All cohesive parameters are directly obtained from mechanical properties of 2D C/SiC composites. Results show that the model can almost reproduce joint shear behaviors and z-pin shear-off failure process. Joint failure results from coupled fiber tensile and fiber–matrix shearing damages at faying plane. The model also successfully demonstrates that joint shear properties can be effectively improved by changing z-pin density and diameter. The relationship between joint properties and mechanical properties of 2D C/SiC composites are subsequently obtained with the model. In this sense, joint shear strength increases with cohesive or in-plane shear strengths of 2D C/SiC composites.     

Effect of carbon nanotubes on the strength of adhesive lap joints of C/C and C/C-SiC ceramic fibre composites

Similar substrates of carbon/carbon (C/C) and carbon/carbon-silicon carbide (C/CSiC) composites were bonded with pure epoxy resin and the one containing 3% multiwall carbon nanotubes (MWCNTs). The results show that MWCNT/filled epoxy resin bonded C/CC/C and C/CSiCC/CSiC substrates have a higher adhesive joint strength than those bonded with epoxy resin alone. MWCNTs increase the toughness and strength of the epoxy resin, which increases the interface bond strength between two similar matching surfaces.     

A new route to fabricate SiB4 modified C/SiC composites

In order to improve the oxidation and thermal shock resistance of 2D C/SiC composites, dense SiB₄–SiC matrix was in situ formed in 2D C/SiC composites by a joint process of slurry infiltration and liquid silicon infiltration. The synthesis mechanism of SiB₄ was investigated by analyzing the reaction products of B₄C–Si system. Compared with the porous C/SiC composites, the density of C/SiC–SiB₄ composites increased from 1.63 to 2.23 g/cm³ and the flexural strength increased from 135 to 330 MPa. The thermal shock behaviors of C/SiC and C/SiC–SiB₄ composites protected with SiC coating were studied using the method of air quenching. C/SiC–SiB₄ composites displayed good resistance to thermal shock, and retained 95% of the original strength after being quenched in air from 1300 °C to room temperature for 60 cycles, which showed less weight loss than C/SiC composite.     

基体改性对碳纤维增韧碳化硅复合材料结构与性能的影响

采用化学气相浸渗法对2D C/SiC复合材料进行基体改性,制备了二维碳纤维增韧碳-碳化硅二元基复合材料(two dimensional carbon fiber reinforced C-SiC binary matrix composites,2D C/C-SiC).2D C/C-SiC复合材料的基体为热解碳和碳化硅交替叠层的多层基体.研究了2D C/C-SiC复合材料的微观结构,比较了2DC/SiC复合材料和2DC/C-SiC复合材料的力学性能及断口形貌.结果表明:2DC/C-SiC复合材料可在基本保持2DC/SiC复合材料抗弯强度的基础上,其断裂韧性得到显著提高.基体改性的效果明显.纤维的逐级拔出是断裂韧性提高的原因.     

Thermal stability of CVI and MI SiC/SiC composites with Hi-Nicalon™-S fibers

The influence of high-temperature argon heat-treatment on the microstructure and room- temperature in-plane tensile properties of 2D woven CVI and 2D unidirectional MI SiC/SiC composites with Hi-Nicalon?-S SiC fibers was investigated. The 2D woven CVI SiC/SiC composites were heat-treated between 1200 and 1600 °C for 1- and 100-hr, and the 2D unidirectional MI SiC/SiC composites between 1315 and 1400 °C for up to 2000 hr. In addition, the influence of temperature on fast fracture tensile strengths of these composites was also measured in air. Both composites exhibited different degradation behaviors. In 2D woven CVI SiC/SiC composites, the CVI BN interface coating reacted with Hi-Nicalon?-S SiC fibers causing a loss in fast fracture ultimate tensile strengths between 1200 and 1600 °C as well as after 100-hr isothermal heat treatment at temperatures > 1100 °C. In contrast, 2D unidirectional MI SiC/SiC composites showed no significant loss in in-plane tensile properties after the fast fracture tensile tests at 1315 °C. However, after isothermal exposure conditions from 1315° to 1400°C, the in-plane proportional limit stress decreased, and the ultimate tensile fracture strain increased with an increase in exposure time. The mechanisms of strength degradation in both composites are discussed.     

碳/碳化硅摩阻复合材料的研究进展

碳/碳化硅是近年来发展起来的一种新型高性能陶瓷基摩阻材料,具有密度低,抗氧化性好,摩擦性能高且性能稳定等一系列优点,在高速列车、飞机和重型汽车等高能载制动领域具有广泛的应用前景.反应性熔体浸渗法是制备碳/碳化硅摩阻复合材料的有效途径.从碳/碳化硅摩阻复合材料的设计出发,深入分析了反应性熔体渗透过程的热力学条件,Si-C反应体系的基本特征以及动力学规律.针对短纤维模压和三维针刺等两种典型C/SiC复合材料的制备过程,对材料的微结构特征和摩擦磨损性能进行了系统论述.同时,对红外热成像、X射线透射和工业CT等先进工程检测方法在碳/碳化硅摩阻复合材料构件上的应用进行了分析.     

In situ growth of a carbon interphase between carbon fibres and a polycarbosilane-derived silicon carbide matrix

An in situ grown carbon interphase between C fibres and a SiC matrix has been produced by impregnation and pyrolysis of a polycarbosilane–xylene solution. The microstructures of the carbon interphase and the effects on the mechanical properties of the C fibre reinforced SiC (C/SiC) composites were investigated using transmission and scanning electron microscopy. It was found that the carbon interphase was a turbostratic carbon with high porosity. The resulting C/SiC composites were found to exhibit improved mechanical properties with respect to the interphase-free composite.     

Siliconization elimination for SiC coated C/C composites by a pyrolytic carbon coating and the consequent improvement of the mechanical property and oxidation resistances

Carbon/carbon (C/C) composites have a wide application as the thermal structure materials because of their excellent properties at high temperatures. However, C/C composites are easily oxidized in oxygen-containing environment, which limits their potential applications to a great degree. Silicon carbide (SiC) ceramic coating fabricated via pack cementation (PC) was considered as an effective way to protect C/C composites against oxidation. But the mechanical properties of C/C composites were severely damaged due to chemical reaction between the molten silicon and C/C substrate during the preparation of SiC coating by PC. In order to eliminate the siliconization erosion, a pyrolytic carbon (PyC) coating was pre-prepared on C/C composites by the chemical vapor infiltration (CVI) prior to the fabrication of SiC coating. Due to the retardation effect of PyC coating on siliconization erosion, the flexural strength retention of the SiC coated C/C composites with PyC coating increased from 46.27 % to 107.95 % compared with the specimen without PyC coating. Furthermore, the presence of homogeneous and defect-free PyC coating was beneficial to fabricate a compact SiC coating without silicon phase by sufficiently reacting with molten silicon during PC. Therefore, the SiC coated C/C composites with PyC coating had better oxidation resistances under dynamic (between room temperature and 1773 K) and static conditions in air at different temperatures (1773?1973 K).     

Effect of initial density on thermal conductivity of new micro-pipeline heat conduction C/SiC composites

C/SiC composites prepared by chemical vapor infiltration technique (CVI) have been regarded as thermal structural materials widely. However, these composites still suffer from poor functional properties like low thermal conductivity, especially in thickness direction of the composites, limiting their large-scale applications. Herein, mesophase pitch based carbon fiber (MPCF) and continuous wave laser machining were utilized to construct highly effective heat conductive micro-pipelines within CVI C/SiC composite. The effect of initial density on the final density and thermal conductivity of the as-obtained MPCF-C/SiC composites were investigated. The results revealed that higher initial density would directly enhance the thermal conductivity and reduce the negative impact of the bottle-neck effect. At temperatures between 100°C and 500°C, MPCF-C/SiC composites preserved more than threefold of the thermal conductivity (340%) when compared to reference C/SiC composites. This work provides a highly effective route for enhancing the thermal conductivity of C/SiC, which would broaden their future applications.     

Ni包裹SiC对SiC(Ni)/Fe复合材料性能的影响

分别以SiC粉体和Ni包裹的SiC复合粉体为硬质相,采用热压工艺(1000°C,20°C/min,40 MPa和45 min)制备了SiC含量为1 wt%~9 wt%的SiC/Fe复合材料。采用扫描电镜(SEM)、能谱仪(EDS)和X射线衍射仪(XRD)等研究了复合材料的界面反应物。研究结果表明:Ni过渡层的存在有效避免了SiC颗粒与Fe基体之间的化学反应。随着Ni包裹SiC粉体含量的增加,复合材料的相对密度和抗弯强度先增加后减小,当SiC(Ni)粉体含量为5 wt%时达到最大值。