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Synthesis of graphene oxides particle of high oxidation degree using a modified Hummers method

X射线光电子能谱 石墨烯 拉曼光谱 热重分析 材料科学 微晶 扫描电子显微镜 氧化物 傅里叶变换红外光谱 分析化学(期刊) 热稳定性 透射电子显微镜 粒径 氧气 核化学 化学工程 化学 纳米技术 有机化学 复合材料 物理 工程类 冶金 光学
作者
Abedalkader Alkhouzaam,Hazim Qiblawey,Majeda Khraisheh,Muataz Ali Atieh,Mohammad A. Al‐Ghouti
出处
期刊:Ceramics International [Elsevier BV]
卷期号:46 (15): 23997-24007 被引量:293
标识
DOI:10.1016/j.ceramint.2020.06.177
摘要

High-oxidation-degree graphene oxide particles were synthesized using a modified Hummers' method. Six different types of particles were synthesized by varying the operating conditions, including the temperature, the reactant ratios, and the oxidation time. The oxidation degree, represented by the oxygen content, and the atomic oxygen/carbon (O/C) ratio were determined using CHNSO elemental analysis, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy-universal attenuated total reflectance sensor (FTIR-UATR) and Raman spectroscopy. The structural morphology of graphene oxide was evaluated using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The thermal stability of the particles was studied using thermogravimetric analysis (TGA). The SEM images showed that the prepared GO samples had different graphitic layer structures. The TEM images showed different stacking levels and transparency of GO flakes caused by the difference in oxidation level. The oxygen content and O/C ratios ranged between 34.7 and 50.0 wt% and 0.43 and 0.8, respectively. The highest oxygen content and O/C ratio were found to be 50 wt% and 0.8, respectively, for GO prepared at 95 °C with a 1-hr reaction time (GO2-a). A quantitative analysis on the FTIR-UATR spectra was performed and was in reasonable agreement with the CHNSO analysis results. The Raman spectra showed two characteristic bands (D and G) with different relative intensities, as characterized by the ID/IG ratio, suggesting that the prepared samples had different crystallite sizes and defects. The crystallite size (La) of the prepared GO particles was estimated using the Tuinstra-Koenig model and were ranging between 9 and 24 nm. The TGA results were correlated with the elemental analysis results and showed a clear dependence of the weight loss on the GO elemental compositions. GO2-a exhibited the lowest thermal stability because of a high oxygen content, whereas GO1-b exhibited the highest thermal stability.
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