Silazane derived ceramics and related materials

被引:417
作者
Kroke, E [1 ]
Li, YL [1 ]
Konetschny, C [1 ]
Lecomte, E [1 ]
Fasel, C [1 ]
Riedel, R [1 ]
机构
[1] Tech Univ Darmstadt, Fachbereich Mat Wissensch, Fachgebiet Disperse Festoffe, D-64287 Darmstadt, Germany
关键词
silazane; polysilazanes; cross-linking; silazane derived ceramics; chemical vapour deposition;
D O I
10.1016/S0927-796X(00)00008-5
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This review highlights the synthesis, processing and properties of non-oxide silicon-based ceramic materials derived from silazanes and polysilazanes. A comprehensive summary of the preparation of precursor compounds containing Si-N-Si units, including commercially available materials, is followed by the discussion of various processing techniques. The fabrication of dense bulk ceramics in the Si/E/C/N systems is reported which involves cross-linking of the polymeric ceramic precursor followed by a polymer-to-ceramic transformation step. The crosslinked precursor can be milled, compacted and pyrolysed to form dense, additive-free, amorphous silicon carbonitride monoliths or polycrystalline composites which withstand oxidation in air at 1600 degrees C. Furthermore, an overview is given on the fabrication of silazane derived powders and coatings involving chemical vapour deposition (CVD) methods utilising volatile precursors. Fibre spinning and fibre properties, as well as other processing techniques like infiltration of preforms, the preparation of porous ceramics and joining are briefly discussed. A state of the art of the mechanical properties of polymer derived amorphous Si/C/N and Si/B/C/N ceramics with respect to hardness as well as high-temperature creep and oxidation resistance is summarised. Finally, some important aspects of industrial applications will be considered. The review is in part based on our own work related to the polysilazane derived ceramics, but will also cover a comprehensive state of the art including the published literature in this field. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:97 / 199
页数:103
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