吸附
植酸
铀
X射线光电子能谱
化学
傅里叶变换红外光谱
核化学
水溶液
选择性
生物吸附
离子交换
无机化学
化学工程
材料科学
有机化学
催化作用
离子
生物化学
冶金
工程类
吸附
作者
Hao Lei,Shuangshuang Huang,Ning Pan,Hao Zou,Xiao Wang,Xianguo Tuo
出处
期刊:ACS ES&T water
[American Chemical Society]
日期:2023-05-05
卷期号:3 (8): 2522-2534
被引量:10
标识
DOI:10.1021/acsestwater.3c00123
摘要
The efficient adsorption and removal of U(VI) from nuclear wastewater is fetching growing interest due to its importance for the ecological environment and human health. In this study, we report a facile ionic self-assembly method to synthesize a phytic acid-based material denoted PE- x using phytic acid and ethylenediamine. PE- x was applied to remove U(VI) from a highly acidic aqueous solution with pH = 1.0. In batch adsorption experiments, PE- x showed fast removal kinetics for U(VI) with an equilibrium time around 10 min, excellent selectivity for An-Ln and U(VI) with a maximum selectivity of 97.8% and 76.2%, and a remarkable maximum adsorption capacity of 689.7 mg/g toward U(VI). Additionally, PE- x exhibited a considerable adsorption capacity of 282.6 mg/g in the fixed bed column test. The adsorption mechanism was investigated by using scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The results indicate a unique mechanism based on the reconstruction of the self-assembly framework involving U(VI) building blocks driven by positively charged species exchange. This study provides new insights and strategies for the design of enhanced uranium adsorbents under highly acidic conditions and extends the potential practical application of phytic acid for uranium capture from radioactive wastewater.
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