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为了使石墨粉体与树脂能够更好地结合,改善碳素制品的性能,首先在石墨粉体中原位合成不同酚醛树脂,再制备成炭/石墨(C/G)复合材料;分析了原位合成不同树脂的热性能,观察了炭/石墨复合材料的微观结构,比较了不同种类、含量的树脂制备炭/石墨复合材料的性能。结果表明:在0~900℃内,原位合成硼改性酚醛树脂(B-PFR)和邻甲环氧酚醛树脂(OCE-PFR)的热稳定性能较热塑性酚醛树脂(TFLPFR)和热固性酚醛树脂(TS-PFR)的好;原位合成的树脂经焙烧后,B-PFR-C/G中石墨颗粒和孔隙分布较均匀,其次为TP-PFR-C/G和TS-PFR-C/G;B-PFR-C/G的综合性能更好,树脂质量分数为359/6时其密度、硬度、抗压强度可分别达到1.58g·cm^-3,47.5HS,31.8MPa。

In order to combine the graphite powders and resin better, improve the performance of carbon product, phenol-formaldehyde resin(PFR)was in-situ synthesized in the graphite powders, which was used to prepare carbon/graphite (C/G) composites. The thermal performance of different resins prepared by in-situ synthesis was analyzed. The microstructure of the composites was observed. The performance of the C/G composites prepared with different kinds and contents resins was compared. The results show that the thermal stability performance of boron PFR(B-PFR) and o-cresol epoxy PFR(OCE-PFR) were better than thermoplastic phenolic (TP) PFR (TP-PFR) and thermosetting(TS) PFR (TS-PFR) in 0~900℃. The graphite granules and holes in B-PFR-C/G distributed more evenly than those in TP-PFR and TS~PFR after calcination. The comprehensive performance of B-PFR-C/G was better, the density, hardness and compressive strength were 1.58g·cm^-3, 47. 5 HS and 31.8 MPa when the resin content was 35wt%.

参考文献

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[4] 曾宪伟,赵东林.碳纳米管/聚苯胺复合材料的原位合成及其形成机理[J].炭素技术,2004(04):15-19.
[5] 李淑君,陶毓博,李坚,刘一星.用TG-DSC-FTIR联用技术研究酚醛树脂的热解行为[J].东北林业大学学报,2007(06):56-58.
[6] 田建华,陈建,徐凤珍,刘锋耀,孙佼.石墨粉体原位合成酚醛树脂制备炭素材料[J].炭素技术,2009(05):7-10.
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