胡阳, 解鑫, 孙春宝, 寇珏. 不同分子结构表面活性剂对低氧化度氧化石墨插层机理的探索[J]. 工程科学学报, 2020, 42(1): 84-90. DOI: 10.13374/j.issn2095-9389.2019.06.03.001
引用本文: 胡阳, 解鑫, 孙春宝, 寇珏. 不同分子结构表面活性剂对低氧化度氧化石墨插层机理的探索[J]. 工程科学学报, 2020, 42(1): 84-90. DOI: 10.13374/j.issn2095-9389.2019.06.03.001
HU Yang, XIE Xin, SUN Chun-bao, KOU Jue. Study of the intercalation mechanisms of surfactants with different molecular structures on mildly oxidized graphite[J]. Chinese Journal of Engineering, 2020, 42(1): 84-90. DOI: 10.13374/j.issn2095-9389.2019.06.03.001
Citation: HU Yang, XIE Xin, SUN Chun-bao, KOU Jue. Study of the intercalation mechanisms of surfactants with different molecular structures on mildly oxidized graphite[J]. Chinese Journal of Engineering, 2020, 42(1): 84-90. DOI: 10.13374/j.issn2095-9389.2019.06.03.001

不同分子结构表面活性剂对低氧化度氧化石墨插层机理的探索

Study of the intercalation mechanisms of surfactants with different molecular structures on mildly oxidized graphite

  • 摘要: 以人造石墨为原料制备了低氧化程度的氧化石墨(MOG),并研究了具有不同极性基团和不同碳链长度的表面活性剂对氧化石墨的插层机理。通过X射线衍射(XRD)、红外光谱(FT-IR)、X射线光电子能谱(XPS)、拉曼光谱(Raman)和Zeta电位仪对插层前后的氧化石墨进行表征,探讨表面活性剂的分子结构对其插层能力的影响以及表面活性剂的插层机理。结果表明阳离子表面活性剂主要通过其极性端与氧化石墨的羧基、羟基之间的静电吸引作用进入氧化石墨层间进行插层,其插层效果优于阴离子表面活性剂,更容易增大氧化石墨的层间距。阴离子表面活性剂则通过与氧化石墨之间形成氢键和疏水作用力来进行插层。研究表明:表面活性剂极性基团的分子大小越大,非极性端的碳链越长,其插层能力越强。上述研究成果有助于深入认识表面活性在氧化石墨层间的插层机理,同时也对氧化石墨插层改性材料的制备和应用具有重要的指导意义。

     

    Abstract: As a star material, graphene has attracted much attention because of its excellent mechanical, optical, electrical, and thermal properties. The chemical conversion of graphene oxide is considered to be a promising approach to economically produce graphene in significant quantities, but the reduced graphene oxide prepared from this method suffers a lot of defects, such as vacancies and the presence of residual oxygen groups. In this case, graphite oxide with a low oxidation degree was used to prepare graphene to decrease the residual oxygen groups and vacancies caused by the removal of oxygen groups during reduction. However, this kind of mildly oxidized graphite (MOG) is hard to exfoliate to prepare graphene oxide; it is necessary to increase the basal spacing of MOG to facilitate the exfoliation. According to the literature, the intercalation of surfactants is usually used to enlarge the basal spacing of graphite and graphite oxide, but the intercalation mechanism of surfactants with different structures in MOG remains unknown. In this work, MOG was prepared from artificial graphite powder, and the intercalations of surfactants with different polar parts and carbon chain lengths on MOG were studied. The effect of surfactant molecular structures on their intercalation ability and the intercalation mechanism were studied through measurements with X-ray diffraction spectroscopy (XRD), Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and Raman and Zeta potential measurements. The results show that the cationic surfactants intercalate MOG mainly through the attractive electrostatic interaction between them, and their intercalation capacity is better than that of anionic surfactants as they can enlarge the basal spacing of MOG more easily. The anionic surfactants intercalated MOG through the formation of hydrogen bonds and the hydrophobic intercalation force between them. It was found that the larger the polar part and the longer the carbon chain, the stronger the intercalation ability of surfactants. These research results may help to better understand the intercalation mechanism of the surface in MOG interlayers and guide the preparation and application of MOG intercalation-modified materials.

     

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