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Influence of Crystallinity of Matrix on Mechanical Properties of Fiber-Reinforced Composites Prepared by Polysilazanes as Matrix Precursor

机译:基质结晶度对聚硅唑烷制备的纤维增强复合材料的力学性能的影响作为基质前体

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摘要

Fiber-reinforced ceramics were fabricated by using pehrydropolysilzane (PHS), polyborosilazane added PHS (PHS-B) or methylhydropolysilazane (MHS) as matrix precursors, and their mechanical properties were investigated with respect to the crystallinity of the matrix. By firing at 1523 K, MHS and PHS-B formed amorphous matrix and gave composites with the flexural strength of 820 and 920 MPa. PHS formed a crystalline matrix and gave a composite with a flexural strength of 450 MPa. The high strength composites may be brought by the lower elastic modulus of amorphous matrix as compared to the crystalline one. Because the low-elastic matrix decreases the stress concentration on fiber due to matrix-cracks. The heat resistance of the composite was tested upon heat exposure at 1523 K for 720 ks. The amorphous composite, fabricated by MHS at 1623 K, endured the heat exposure and retained 77% of its initial strength.
机译:通过使用Pehrydropolysilzane(pHS),聚硼腙添加的pH(pHS-B)或甲基氢聚硅氮烷(MHS)作为基质前体来制造纤维增强陶瓷,并相对于基质的结晶度研究其机械性能。 通过在1523K,MHS和PHS-B处烧制,形成无定形基质,并在弯曲强度为820和920MPa的复合材料中进行。 PHS形成了结晶基质,并通过450MPa的弯曲强度得到复合材料。 与结晶物相比,高强度复合材料可以通过无定形基质的较低弹性模量引起。 因为低弹性基质由于基质裂纹而降低光纤上的应力浓度。 在1523k的热暴露于720ks时测试复合材料的耐热性。 由MHS制造的无定形复合材料在1623 k下,耐热曝光,并保留了其初始强度的77%。

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