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Efficient uranium(VI) recovery from fluorinated wastewater via deferiprone ligand complexation
Water Research ( IF 11.4 ) Pub Date : 2024-11-29 , DOI: 10.1016/j.watres.2024.122884
Juanlong Li, Yezi Hu, Zewen Shen, Huihui Jin, Rong He, Wenkun Zhu, Guixia Zhao, Zhuoyu Ji, Bin Ma, Xiangke Wang

Extracting uranium (U(VI)) from fluoride-rich radioactive wastewater is of great significance for the development of nuclear energy and environmental remediation. The presence of thermodynamically stable [UO2Fn]2−n (n = 0, 1, 2, 3, 4) aqueous complexes in fluoride-rich U(VI)-containing wastewater significantly hinders the efficiency of uranyl extraction and recovery using conventional methods. In this study, we report a direct precipitation method using deferiprone ligands for efficient uranyl extraction from fluoride-rich wastewater that offsets the preparation of solid materials. The deferiprone ligands exhibited exceptional chelating ability competing toward F. In simulated 2.1 × 10–4 mol/L U(VI) wastewater with F concentrations ranging from 1 to 10 g/L, adjusting the amount of deferiprone ligands enabled a high U(Ⅵ) precipitation rate of 97.60 % to 86.90 %, correspondingly. A remarkable 99.71 % recovery of U(Ⅵ) from real fluoride-rich alkaline wastewater was achieved within 2 h. Detailed investigations revealed that the competitive chelating by deferiprone ligands results in the formation of insoluble U(VI)-deferiprone complexes ([(UO2)(H2O)(C7NO2H8)2]·4H2O), driven by π-π stacking interactions, electrostatic attractions, and intermolecular hydrogen bonds. Given the cost-efficiency and excellent radiation resistance of deferiprone ligands, this efficient and straightforward precipitation approach holds great promise for practical applications in U(VI) remediation and resource recovery from fluoride-rich wastewater.

中文翻译:


通过去铁酮配体络合从含氟废水中高效回收铀 (VI)



从富氟放射性废水中提取铀 (U(VI)) 对核能开发和环境修复具有重要意义。在富含氟化物的 U(VI) 废水中存在热力学稳定的 [UO2Fn]2−n (n = 0, 1, 2, 3, 4) 水复合物,这严重阻碍了使用传统方法提取和回收铀酰的效率。在这项研究中,我们报道了一种使用去铁酮配体的直接沉淀方法,用于从富含氟化物的废水中高效提取铀酰,从而抵消了固体材料的制备。去铁酮配体表现出对 F- 的异常螯合能力。在模拟的 2.1 × 10–4 mol/L U(VI) 废水中,F− 浓度为 1 至 10 g/L,调整去铁酮配体的量可相应地实现 97.60 % 至 86.90 % 的高 U(VI.) 沉淀率。在 2 小时内,从真正富含氟化物的碱性废水中实现了 99.71% 的 U(VI.) 回收率。详细研究表明,去铁酮配体的竞争性螯合导致不溶性 U(VI)-去铁酮复合物 ([(UO2)(H2O)(C7NO2H8)2]·4H2O),由 π-π 堆积相互作用、静电吸引力和分子间氢键驱动。鉴于去铁酮配体的成本效益和出色的抗辐射性,这种高效而直接的沉淀方法在铀(VI) 修复和从富含氟化物的废水中回收资源方面具有很大的前景。
更新日期:2024-11-29
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