Molecule editable 3D printed polymer-derived ceramics

被引:63
|
作者
Zhou, Shixiang [1 ]
Mei, Hui [1 ]
Chang, Peng [1 ]
Lu, Mingyang [1 ]
Cheng, Laifei [1 ]
机构
[1] Northwestern Polytech Univ, Sch Mat Sci & Engn, Sci & Technol Thermostruct Composite Mat Lab, Xian 710072, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
3D printing; Polymer-derived ceramics; Preceramic polymers; Structuralization; PRECERAMIC POLYMERS; MANUFACTURING TECHNIQUES; ABSORPTION PROPERTIES; SILICON-CARBIDE; SIOC CERAMICS; SIC NANOWIRES; FABRICATION; COMPONENTS; SCAFFOLDS; PERFORMANCE;
D O I
10.1016/j.ccr.2020.213486
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
With the demand for advanced ceramics applied under harsh conditions, highly reliable ceramic components with customized structures and specific functions are in increasing demand. 3D printing can realize an integrated design of articles from macroscale to micro-/nanoscale, as it has outstanding design flexibility, near net-shape forming, and mold-free fabrication. However, traditional ceramic raw materials are usually ceramic powders, which are hard to meet the requirements of specific 3D printing techniques. Preceramic polymers as a special precursor are suitable for a series of forming methods including 3D printing, as they can be manipulated in polymeric phases. More importantly, the molecule of preceramic polymers are editable and designable, which can meet the requirements of various 3D printing techniques by molecule modification. Desired compositions and functions can be obtained by reacting with fillers and doping metals, realizing the integrated design of function and structure. This review investigated the polymer-derived ceramics (PDC) which are formed via 3D printing techniques. Differences between ceramic powders and preceramic polymers were presented, the superiority and drawbacks of the preceramic polymers were illustrated, which may facilitate the material selection, structure design, and fabrication of reliable and tailor-made 3D printed PDC components. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页数:20
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