铀酰
吸附
海水
化学
铀
氢键
无机化学
化学工程
分子
核化学
有机化学
材料科学
地质学
冶金
海洋学
工程类
作者
Ying Wang,Zaiwen Lin,Jiahui Zhu,Jingyuan Liu,Jing Yu,Qi Liu,Rongrong Chen,Ying Li,Jun Wang
标识
DOI:10.1016/j.jhazmat.2022.129407
摘要
Efficiently capturing of uranium (VI) [U(VI)] from seawater elicits unparalleled attraction for sustaining the uplifted requirement for nuclear fuel. However, obtaining the abundant U(VI) resource from seawater has always seriously restricted by competitive adsorption from higher concentrations of competitors, especially vanadium (V) [V(V)]. Herein, based on amidoximized natural bamboo strips with hierarchical porous structure, the molecular-level uranyl-specific "nano-holes" was co-constructed by the intramolecular hydrogen bonds for specifically trapping U(VI) from seawater. Manipulating the branched degrees of amino groups enabled the creation of a series of the molecular-level uranyl-specific "nano-holes" that exhibit ultrahigh affinity and selective adsorption of U(VI) with a adsorption capacity 1.8 fold higher compared to that of V(V) after 30 days floating in the Yellow Sea basin, conquering the long-term challenge of the competitive adsorption of V(V) for amidoxime-based adsorbents applied to extract U(VI) from seawater. The diameter of the molecular-level uranyl-specific "nano-holes" is approximately 12.07 Å, significantly larger than (UO2)3(OH)3+ (10.37 Å) and smaller than HV10O285-, thereby exhibiting specifically trapping of U(VI) in a series of adsorption experiments with different U(VI)-V(V) ratios. Besides, the adsorption model based on the combination of experimental and theoretical results is accompanied by "hydrogen bond breaking and coordination bond formation".
科研通智能强力驱动
Strongly Powered by AbleSci AI