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Developing novel adsorbents for efficient U(VI) adsorption from wastewater is of great significance in both nuclear energy development and environmental protection. Herein, a novel functional resin (AO67/MA33-resin) with large particle size (100–200 μm) was controllably synthesized and employed for U(VI) elimination. The AO67/MA33-resin overcomes the shortcoming of small particle size of traditional adsorbents and shows strong antacid and high-temperature resistance stability and reusability. Meanwhile, the AO67/MA33-resin also exhibits excellent U(VI) removal ability including wide pH adaptability, fast adsorption kinetic, and high adsorption capacity. The adsorption mechanism was determined to involve chelation between amidoxime carboxyl functional groups and uranyl ions. A further application for U(VI) removal from real uranium mine wastewater was evaluated by dynamic column experiments. The present work indicated that the AO67/MA33-resin would be a promising adsorbent material for uranium removal from wastewater. [ABSTRACT FROM AUTHOR]

Removal of uranium from radioactive wastewater with TPEAC. [Display omitted] • A phosphine-oxime modified adsorbent (TPEAC) was successfully prepared. • TPEAC exhibited exceptional selectivity and efficiency for adsorption of uranium. • TPEAC displayed a high recovery of 99.6% using real uranium mining wastewater. • Adsorption mechanism was elucidated through experiments and characterization. Efficient removal of uranium from radioactive wastewater is paramount for the sustainable development of nuclear energy. However, the exploitation of superior adsorbents with practical applications remains a challenge. In this work, we engineered and synthesized an adsorbent (TPEAC) enriched with phosphine-oxime, featuring a matrix composed of hydrophilic modified amidoxime functional groups. TPEAC exhibited exceptional selectivity (Multiple ion coexistence R% > 99 %) and efficiency in uranium adsorption, with a higher adsorption rate (reach equilibrium around 400 mins) and capacity (243.9 mg/g) than raw-amidoxime (133.3 mg/g) and modified-amidoxime (175.4 mg/g) materials. Moreover, it maintained robust stability and reusability even after six adsorption–desorption cycles, with removal ratio still above 95 %. In-depth mechanistic investigations through DFT and XPS elucidated that P-O (P=O) groups exhibited a stronger affinity for U(VI) compared to other functional groups, and the adsorption of TPEAC towards U(VI) primarily due to the synergistic interaction among P-O (P=O) groups, C(NH 2) = N-OH, and carboxyl groups, which significantly facilitated the effective removal of U(VI). Most prominently, TPEAC performed considerable potential in processing actual uranium mine wastewater, with its dynamic column device achieving a U(VI) recovery up to 99.6 %. This work not only furnishes an efficacious and economical solution for uranium wastewater treatment but also provides new approaches for scalable application uranium materials. [ABSTRACT FROM AUTHOR]