Long-term oxidation behaviors and strength retention properties of self-healing SiCf/SiC-SiBCN composites

被引:16
作者
Ji, Suya [1 ,2 ]
Liang, Bin [1 ]
Yang, Bin [1 ,3 ]
Hu, Chenglong [1 ]
Jiang, Yan [1 ,4 ]
Pang, Shengyang [1 ]
Li, Jian [1 ]
Zhao, Rida [1 ,2 ]
Tang, Sufang [1 ]
机构
[1] Chinese Acad Sci, Inst Met Res, Shi Changxu Innovat Ctr Adv Mat, Shenyang 110016, Peoples R China
[2] Univ Sci & Technol China, Sch Mat Sci & Engn, Shenyang 110016, Peoples R China
[3] AECC Guizhou Liyang Aviat Power Co Ltd, Guiyang 550014, Guizhou, Peoples R China
[4] Shenyang Univ Chem Technol, Dept Mat Sci & Engn, Shenyang 110142, Peoples R China
基金
中国国家自然科学基金;
关键词
CVI3PIP; Self-healing; Oxidation; Strength retention; SiCf; SiC-SiBCN; SIC MATRIX COMPOSITES; SIC/SIC COMPOSITES; MECHANICAL-PROPERTIES; CREEP-BEHAVIOR; FIBER; TEMPERATURE; CVI; MICROSTRUCTURE; INFILTRATION; INTERPHASES;
D O I
10.1016/j.jeurceramsoc.2022.12.009
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The self-healing SiCf/SiC-SiBCN composites with various boron contents in SiBCN were prepared, and their long-term oxidation behaviors and strength retention properties were investigated. The 100 h oxidation at 1200-1350 degrees C leads to parabolic mass gain of the obtained composites. With the oxidation temperature increased from 1200 degrees C to 1350 degrees C, the oxidation rate constants increase from 5.91 x 10-8 mg2/(mm4 h) to 9.31 x 10-7 mg2/(mm4 h) for the boron-lean (3.14%) composites, and from 2.57 x 10-7 mg2/(mm4 h) to 6.04 x 10-7 mg2/ (mm4 h) for the boron-rich (7.18 wt%) composites. Correspondingly, the oxidation activation energy decreases from 363 kJ/mol to 112 kJ/mol due to the low initial oxidation temperature of boron-rich SiBCN. All the composites exhibit the higher strength retention rates after 1350 degrees C oxidation due to the enhanced self-healing performance. The boron-rich composites show a high strength retention rate of up to 104% due to the good self-healing capacity of the boron-rich SiBCN as well as the high CVI-SiC content.
引用
收藏
页码:1843 / 1852
页数:10
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