Microstructure and mechanical properties of pitch based mixture modified by additions of graphene oxide precursor and TiB2 particles

石墨烯 微观结构 氧化物 材料科学 化学工程 纳米技术 氧化石墨烯纸 复合材料 冶金 工程类
作者
Cheng Zhang,Zengjie Wang,Jilai Xue,Xuan Liu,Yanan Zhang,Xiang Li
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:443: 136402-136402 被引量:4
标识
DOI:10.1016/j.cej.2022.136402
摘要

• Graphene Oxide (GO) modified coal tar pitch (CTP) increases its modulus and L a . • TiB 2 addition improves the ultimate strain and L c of carbon matrix in CTP. • Synergistic GO-TiB 2 addition has improved mechanical property and microstructure. • TiB 2 plays a key role in reducing C–C bonds oxidation and enhancing strength. Pitch based mixture as binder material is crucial component for structure stability and mechanical properties of carbon/graphite electrodes. In this work, coal tar pitch (CTP) mixture was modified by additions of graphene oxide (GO) precursor and fine TiB 2 particles. It is found that 1 wt.%GO addition increases the crystallite size, L a value and reduce the defects density of (0 0 2) planes in CTP mesophase and carbonization products with increased elastic modulus. The additions of 3 or 5 wt.%TiB 2 increase the stacking height of (0 0 2) planes ( L c ) of CTP pyrolysis and carbonization products with increased edge dislocation density and ultimate strain. The combined additions of TiB 2 and GO generate a synergistic effect on further improving the mechanical properties of CTP carbonization products with increasing the stacking order of (0 0 2) plane, crystallite size ( L a and L c ) and edge dislocation density. CTP-1GO-5TiB 2 shows a compressive strength 194.7 MPa higher than the pure CTP (155.4 MPa). Further findings suggest that a combined mechanism of GO and TiB 2 additions can be established through stabilizing C–C bonds while reducing C-O bonds along with chemical component transformations after pyrolysis and carbonization. TiB 2 particles play a key role in making the synergistic effect on improving the mechanical strength and reducing the oxidation of C–C bonds with additional increase in L a value.

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