化学
铀酰
铀
吸附
离子键合
萃取(化学)
纳米技术
石墨烯
解吸
扩散
海水
化学物理
无机化学
化学工程
离子
物理化学
色谱法
有机化学
热力学
冶金
地质学
工程类
物理
材料科学
海洋学
作者
Zeyu Wang,Rongchen Ma,Qinghao Meng,Yajie Yang,Xujiao Ma,Xianghui Ruan,Ye Yuan,Guangshan Zhu
摘要
High-speed capturing of uranyl (UO22+) ions from seawater elicits unprecedented interest for the sustainable development of the nuclear energy industry. However, the ultralow concentration (∼3.3 μg L-1) of uranium element leads to the slow ion diffusion inside the adsorbent particle, especially after the transfer paths are occupied by the coexisted interfering ions. Considering the geometric dimension of UO22+ ion (a maximum length of 6.04-6.84 Å), the interlayer spacing of graphene sheets was covalently pillared with phenyl-based units into twice the ionic length (13 Å) to obtain uranyl-specific nanofluidic channels. Applying a negative potential (-1.3 V), such a charge-governed region facilitates a unipolar ionic transport, where cations are greatly accelerated and co-ions are repelled. Notably, the resulting adsorbent gives the highest adsorption velocity among all reported materials. The adsorption capacity measured after 56 days of exposure in natural seawater is evaluated to be ∼16 mg g-1. This novel concept with rapid adsorption, high capacity, and facile operating process shows great promise to implement in real-world uranium extraction.
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