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Surface modification of carbon fibers with hydrophilic Fe_3O_4 nanoparticles for nickel-based multifunctional composites

机译:碳纤维与亲水Fe_3O_4纳米颗粒的表面改性镍基多官能复合材料

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Grafting functional components onto carbon fibers is important for designing many multifunctional composites. However, this process is often hindered by the low reactivity of carbon fibers. Hence, developing innovative grafting strategies with functional groups or nanomaterials on carbon fibers (CFs) is highly desired. Herein, we proposed a facile method to grow hydrophilic Fe3O4 NPs on non-pretreated CFs using a polyol-assisted hydrothermal method, changing hydrophobic CFs to hydrophilic. Benefiting from the hydrophilic property of CFs@Fe3O4, the resultant CFs@Fe3O4 can be successfully coated by SiO2 layer to form CFs@Fe3O4@SiO2 composites. After a hydrothermal reaction with nickel ions, the CFs@Fe3O4@nickel silicate composites were fabricated. Followed by coating polydopamine (PDA) layer and then carbonizing in N2 atmosphere, CFs@Fe3O4@SiO2-C/Ni hybrids can be finally obtained. Notably, the hydrophilic Fe3O4 NPs play a crucial role in the fabrication process, not only improving the interfacial adhesion of carbon fibers for further modification but also providing the main magnetism resource. Moreover, the density and size of Ni NPs can be tailored by tuning pyrolysis temperature. Experimental results confirm that CFs@Fe3O4@SiO2-C/Ni hybrids synthesized at 700 degrees C gave the best activity on the reduction in 4-nitrophenol, which are easy to collect and recycle due to their unique structure and good magnetic property.
机译:将功能性分配到碳纤维上对于设计许多多功能复合材料是重要的。然而,该过程通常受碳纤维的低反应性阻碍。因此,非常需要在碳纤维上的官能团或纳米材料(CFS)中发展创新的接枝策略。在此,我们提出了使用多元醇辅助水热法在非预处理的CFS上生长亲水性Fe3O4 NPS的容纳方法,改变疏水性CFS至亲水性。受益于CFS @ Fe3O4的亲水性,得到的CFS @ Fe3O4可以通过SiO 2层成功涂覆,形成CFS @ Fe3O4 @ SiO2复合材料。在与镍离子的水热反应后,制备CFS @ Fe3O4镍硅酸盐复合材料。然后通过涂覆多碳胺(PDA)层,然后在N 2气氛中碳化,最终可以获得CFS @ Fe3O4杂交杂种。值得注意的是,亲水性Fe3O4 NPS在制造过程中发挥至关重要的作用,不仅提高了碳纤维的界面粘附,而且还提供了主要磁力资源。此外,可以通过调节热解温度来定制Ni NP的密度和尺寸。实验结果证实,在700摄氏上合成的CFS @ Fe3O4 @ SiO2-C / Ni杂种在4-硝基苯酚的还原中获得了最佳活性,这易于收集和再循环,因为它们的独特结构和良好的磁性。

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