萃取(化学)
铀
离子
离子液体
离子键合
超短脉冲
无机化学
化学
材料科学
有机化学
激光器
冶金
催化作用
光学
物理
作者
Jing He,Jia Chen,Yongxing Sun,Zijie Li,Huifeng Liu,Juanjuan Wang,Wei‐Qun Shi,Hongdeng Qiu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2025-08-01
卷期号:18 (12): 94907856-94907856
被引量:1
标识
DOI:10.26599/nr.2025.94907856
摘要
Uranium extraction from seawater (UES) is crucial for reducing nuclear fuel supply pressure and promoting the comprehensive utilization of marine resources. The successful implementations of UES engineering critically relies on the highly efficient sorbent materials with exceptional performance in binding uranyl ions. Herein, a universal and facile “organic ion building blocks self-assembly” strategy is established to realize a first class of carboxyl functionalized ionic single crystals, named BPTC-BPY-R (R=1-6), derived from rationally designed viologen-derivatives with different alkyl chain lengths and polycarboxylic acid. This strategy effectively exploits the organic ion building block properties to achieve U(VI) adsorption based on the synergistic effects of anions (ligand interaction) and cations (electrostatic interaction). Notably, attributed to the special crystal stacking mode and higher specific surface area, the resulting BPTC-BPY-3 not only achieves ultrahigh selectivity for U(VI) adsorption with a partition coefficient of 3.998×106 mL/g, but also possesses an ultrafast U(VI) adsorption kinetics and an uptake capacity of 686.8 mg/g within 2 min. More importantly, it realized a U(VI) uptake capacity of 7.41 mg/g from natural seawater in 20 days. The designed material with ultra selectivity, high capacity, ultrafast kinetics, and good recyclability exhibits a great promise for efficient U(VI) extraction from seawater.
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