Microstructure and properties of PAN-based carbon fiber with different graphitization temperature (up to 3000 °C)

被引:0
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作者
Jiang, Zhenyu [1 ]
Chen, Qiufei [1 ]
Fan, Baolin [5 ]
He, Jian [1 ]
Malik, Hamza [1 ]
Zhang, Hui [1 ,2 ,3 ]
Liu, Yong [1 ,2 ,3 ]
Yu, Jianyong [4 ]
机构
[1] State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai,201620, China
[2] The Key Laboratory of High-Performance Fiber and Product, Ministry of Education, College of Materials Science and Engineering, Donghua University, Shanghai,201620, China
[3] Shanghai High Performance Fibers and Composites Center (Province-Ministry Joint), Donghua University, Shanghai,201620, China
[4] Innovation Center for Textile Science and Technology, Donghua University, Shanghai,201620, China
[5] Zhongfu Shenying Carbon Fiber Co.,ltd., Lianyungang,222000, China
关键词
D O I
10.1016/j.diamond.2025.111953
中图分类号
学科分类号
摘要
Understanding and regulating the graphitization process are critical to high-modulus carbon fiber production technologies. In this work, a series of high modulus polyacrylonitrile (PAN)-based carbon fibers (CFs) were prepared via the graphitization process at different temperatures up to 3000 °C in a continuous production line, and the evolution mechanism of the microstructures was investigated. The results showed that the primary reaction at the temperature of 2300–2600 °C is the condensation between graphite molecules, and over 2700 °C is mainly the growth and accumulating of crystallite. Moreover, due to the difference in graphitization difficulty between the skin and core layer of the CFs, the degree of graphitization at the surface is higher than that in the core. SAXS analysis suggests that the transition of amorphous carbon may begin near the micropores due to the sufficient space to rearrangement, and the amorphous carbon can more easily convert to graphite carbon above 2700 °C. Additionally, the optimization of CF microstructures leads to an increase in both tensile strength and elastic modulus with rising graphitization temperatures above 2700 °C. © 2025 Elsevier B.V.
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