吸附
水溶液
氢氧化物
离子强度
化学工程
纳米复合材料
解吸
朗缪尔吸附模型
X射线光电子能谱
甲基橙
核化学
化学
吸附
无机化学
有机化学
催化作用
工程类
光催化
作者
Dongxu Yang,Shuang Song,Yidong Zou,Xiangxue Wang,Shujun Yu,Tao Wen,Hongqing Wang,Tasawar Hayat,Ahmed Alsaedi,Xiangke Wang
标识
DOI:10.1016/j.cej.2017.03.158
摘要
Hierarchical silicon [email protected] double hydroxide (SiO2@LDH) nanocomposites were synthesized by a facile in situ co-precipitation method, and characterized by XRD, FESEM, FT-IR and XPS in detail. The sorption of uranium (U(VI)) and methyl orange (MO) on SiO2@LDH were investigated as a function of pH, ionic strength, contact time and temperature. The results indicated that the sorption of U(VI) and MO were strongly dependent on pH, and weakly dependent on ionic strength, demonstrating that the interaction of U(VI) was mainly dominated by inner-sphere surface complexation and the sorption of MO was mainly attributed to electrostatic attraction due to the high removal efficiency (∼98% within 4 h for U(VI) ions, and ∼92% within 10 min for MO). The kinetics sorption of U(VI) and MO both followed the pseudo-second-order model well, suggesting that the sorption processes were chemical sorption. The sorption isotherms of U(VI) and MO on SiO2@LDH were well fitted by the Langmuir model, and the maximum sorption capacities of SiO2@LDH were calculated to be 303.1 mg·g−1 for U(VI) and 166.1 mg·g−1 for MO. The thermodynamic parameters revealed that the sorption of U(VI) and MO was spontaneous process. Integrating the experimental result analysis, the hierarchical SiO2@LDH may be a promising material for the efficient elimination of radionuclides and dyes from aqueous solutions in natural environmental pollution cleanup.
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