School of Environmental Science and Engineering, Guangzhou University, Guangzhou, 510006, China; Guangdong Provincial Key Laboratory of Radionuclides Pollution Control and Resources, Guangzhou, 510006, China.
School of Environmental Science and Engineering, Guangzhou University, Guangzhou, 510006, China.
Chemosphere. 2020 Nov;258:127152. doi: 10.1016/j.chemosphere.2020.127152. Epub 2020 Jun 6.
Graphene oxide (GO) has been proved with favorable affinity to U(VI), while some drawbacks such as poor dispersity and low adsorption performance limit its application. Herein, cetyltrimethylammonium bromide (CTAB) modified graphene oxide (MGO) composites were successfully fabricated, characterized and compared with graphene oxide (GO) in the sequestration of U(VI) in aqueous solutions. The results showed that maximum adsorption rate of MGO (99.21%) was obviously higher than that of GO (66.51%) under the same initial condition. Simultaneous introduction of C-H and NO coupled with the enhanced dispersity of GO after modification were mainly responsible for the updated performance verified with multiple characterization techniques. Based on the results of kinetics and isotherms investigations, the experimental data were best described by Pseudo-first-order kinetic model and Redlich-Peterson isotherm model. The results of ΔH, ΔS and ΔG show that adsorptive behaviors of uranyl ion on MGO are endothermic and spontaneous. The study provides a feasible alternative to the chemical modification of GO and enhancing the performance towards uranyl ion removal from solution.
氧化石墨烯(GO)已被证明对 U(VI) 具有良好的亲和力,但其分散性差、吸附性能低等缺点限制了其应用。本文成功制备了十六烷基三甲基溴化铵(CTAB)改性氧化石墨烯(MGO)复合材料,并将其在水溶液中吸附 U(VI)的性能与氧化石墨烯(GO)进行了比较。结果表明,在相同的初始条件下,MGO 的最大吸附率(99.21%)明显高于 GO(66.51%)。改性后 C-H 和 NO 的同时引入以及 GO 分散性的增强,是经过多种表征技术验证的更新性能的主要原因。基于动力学和等温线研究的结果,实验数据最好用拟一级动力学模型和 Redlich-Peterson 等温模型来描述。ΔH、ΔS 和 ΔG 的结果表明,铀酰离子在 MGO 上的吸附行为是吸热和自发的。该研究为 GO 的化学改性提供了一种可行的替代方法,并提高了从溶液中去除铀酰离子的性能。