Zhang Zhi-Hui, Lan Jian-Hui, Yuan Li-Yong, Sheng Pan-Pan, He Ming-Yang, Zheng Li-Rong, Chen Qun, Chai Zhi-Fang, Gibson John K, Shi Wei-Qun
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University, Changzhou 213164, China.
Laboratory of Nuclear Energy Chemistry, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.
ACS Appl Mater Interfaces. 2020 Mar 25;12(12):14087-14094. doi: 10.1021/acsami.0c02121. Epub 2020 Mar 10.
Although metal-organic frameworks (MOFs) have been reported as important porous materials for the potential utility in metal ion separation, coordinating the functionality, structure, and component of MOFs remains a great challenge. Herein, a series of anionic rare earth MOFs (RE-MOFs) were synthesized via a solvothermal template reaction and for the first time explored for uranium(VI) capture from an acidic medium. The unusually high extraction capacity of UO (e.g., 538 mg U per g of Y-MOF) was achieved through ion-exchange with the concomitant release of MeNH, during which the uranium(VI) extraction in the series of isostructural RE-MOFs was found to be highly sensitive to the ionic radii of the metal nodes. That is, the uranium(VI) adsorption capacities continuously increased as the ionic radii decreased. In-depth mechanism insight was obtained from molecular dynamics simulations, suggesting that both the accessible pore volume of the MOFs and hydrogen-bonding interactions contribute to the strong periodic tendency of uranium(VI) extraction.
尽管金属有机框架材料(MOFs)作为用于金属离子分离潜在应用的重要多孔材料已有报道,但协调MOFs的功能、结构和组成仍然是一项巨大挑战。在此,通过溶剂热模板反应合成了一系列阴离子型稀土金属有机框架材料(RE-MOFs),并首次探索了其从酸性介质中捕获铀(VI)的性能。通过离子交换并伴随甲胺(MeNH)的释放,实现了对UO异常高的萃取容量(例如,每克Y-MOF可萃取538毫克铀),在此过程中发现该系列同构RE-MOFs中铀(VI)的萃取对金属节点的离子半径高度敏感。也就是说,随着离子半径减小,铀(VI)的吸附容量不断增加。通过分子动力学模拟获得了深入的机理见解,表明MOFs的可及孔体积和氢键相互作用都有助于铀(VI)萃取的强烈周期性趋势。