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-MoO3–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 (UO2Fx), 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-MoO3–x nanosheets exhibited a removal efficiency of 95.3% for uranium, which was much higher than that of MoO3–x. Furthermore, the U-MoO3–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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