铀酰
铀
化学
氧化铀
电化学
钼
核燃料
氟化物
萃取(化学)
无机化学
核化学
氧化物
锕系元素
贫化铀
硝酸铀酰
放射化学
核后处理
氟
废水
二氧化铀
作者
P. Li,Xue Wang,Ru Cheng,Lechang Xu,Han Yang,Xiangyu Shen,Jie Kang,Wenkun Zhu,Rong Liang He
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2026-01-21
卷期号:65 (4): 2238-2247
被引量:2
标识
DOI:10.1021/acs.inorgchem.5c04770
摘要
Electrochemical uranium extraction represents a powerful means to achieve the recovery of uranium resources from nuclear wastewater, but the formation of a complex between fluoride and uranyl in common wastewater severely decreases the extraction efficiency. Herein, the isolated uranyl was predoped in O-vacancy-containing molybdenum oxide (U-MoO 3– x, x < 3) to efficiently electrochemical extract uranium from fluoride-containing nuclear wastewater. In this system, the doped isolated uranyl and the vacancy of the O can strongly bind with the fluorine and uranyl in uranyl fluoride (UO 2 F x ), respectively, enabling the synergistic trapping of dominant species in fluoride-containing nuclear wastewater. With the coexistence of high concentration of fluoride (3 g/L), the U-MoO 3– x nanosheets exhibited a removal efficiency of 95.3% for uranium, which was much higher than that of MoO 3– x . Furthermore, the U-MoO 3– x nanosheets displayed robust uranium extraction performance with a negligible influence of pH variations, interfering ions, and U/F ratios. This work provides a new strategy of preintroduction of uranyl species for promoted electrochemical uranium extraction in a complex environment.
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