Low-temperature chemical vapour curing using iodine for fabrication of continuous silicon carbide fibres from low-molecular-weight polycarbosilane

被引:34
作者
Hong, Junsung [1 ]
Cho, Kwang-Yeon [2 ]
Shin, Dong-Geun [3 ]
Kim, Jeong-Il [4 ]
Oh, Sung-Tag [1 ]
Riu, Doh-Hyung [1 ]
机构
[1] Seoul Natl Univ Sci & Technol, Dept Mat Sci & Engn, Seoul 139743, South Korea
[2] Korea Inst Ceram Engn & Technol, Nano Convergence Intelligence Mat Team, Seoul 153801, South Korea
[3] Korea Inst Ceram Engn & Technol, Energy Efficient Mat Team, Seoul 153801, South Korea
[4] DDACC, Jeon Ju 561844, Jeon Buk, South Korea
关键词
NUCLEAR-MAGNETIC-RESONANCE; HIGH-TENSILE STRENGTH; C-N CERAMICS; PYROLYSIS PROCESS; PRECURSOR; CONVERSION; MECHANISM; NMR; CARBONIZATION; EVOLUTIONS;
D O I
10.1039/c3ta13727a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In order to manufacture fine and continuous silicon carbide (SiC) fibres from low-molecular-weight polycarbosilane (PCS), a new chemical vapour curing process based on the use of iodine was developed. Its main advantages are short processing-time (similar to 1 h) and low processing-temperature (similar to 100 degrees C). The underlying curing mechanism was investigated by performing TG-DTA, GC-MS, solid-state NMR, FTIR, FE-EPMA, ESR, elemental analysis, and XRD. The results indicate that the curing reaction occurs upon diffusion of iodine into the PCS, where iodine plays the critical role of accelerating the cleavage of Si-H (mainly), Si-Si, and C-H bonds. This cleavage coincides with recombination to form cross-linked networks of -Si-C- and -C=C-. The by-products were identified as oligomeric silanes, iodomethane, and aromatics. When the curing is conducted in air, the surface region in contact with oxygen is heavily oxidized to form a Si-O-Si network that is localized on the surface.
引用
收藏
页码:2781 / 2793
页数:13
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