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In situ synthesis of nano size silicon carbide and fabrication of C-SiC composites during the siliconization process of mesocarbon microbeads preforms

机译:中碳微珠预成型件硅化过程中的纳米碳化硅原位合成及C-SiC复合材料的制备

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摘要

C-SiC composites with carbon-based mesocarbon microbeads (MCMBs) preforms are a new type of high-performance and high-temperature structural materials for aerospace applications. In the present study, MCMB-SiC composites were fabricated by liquid silicon infiltration (LSI). Physical and mechanical properties such as density, porosity and bending strength were measured before and after siliconization. The results show the C-SiC composites have excellent bending strength, density and porosity of 210 MPa, 2.41 g/cm3 and 0.62%, respectively. The chemical analysis shows that the composite is composed of 89% SiC, 2% Si and 9% C. The microstructural results also show the existence of two different areas of SiC, one zone of coarse micron size SiC at SiC-Si interface and the other zone consists of fine nano-SiC particles at SiC-C interfaces. The formation mechanism governing the siliconization of porous MCMB preform was also investigated.
机译:具有碳基中碳微珠(MCMBs)预成型体的C-SiC复合材料是一种新型的高性能,高温结构材料,用于航空航天应用。在本研究中,MCMB-SiC复合材料是通过液态硅渗透(LSI)制成的。在硅化之前和之后测量物理和机械性能,例如密度,孔隙率和弯曲强度。结果表明,C-SiC复合材料的抗弯强度,密度和孔隙率分别为210 MPa,2.41 g / cm3和0.62%。化学分析表明,该复合材料由89%的SiC,2%的Si和9%的C组成。显微组织结果还表明,存在两种不同的SiC区域,在SiC-Si界面处有一个微米级的SiC区域,其他区域由SiC-C界面处的细纳米SiC颗粒组成。还研究了控制多孔MCMB预成型件硅化的形成机理。

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