苯并恶唑
铀
共价键
吸附
共轭体系
化学
材料科学
无机化学
核化学
组合化学
有机化学
聚合物
冶金
作者
Wei‐Rong Cui,Cheng‐Rong Zhang,Rui‐Han Xu,Xiao‐Rong Chen,Runhan Yan,Wei Jiang,Ru‐Ping Liang,Jian‐Ding Qiu
出处
期刊:Small
[Wiley]
日期:2021-01-20
卷期号:17 (6): e2006882-e2006882
被引量:152
标识
DOI:10.1002/smll.202006882
摘要
The inherent features of covalent organic frameworks (COFs) make them highly attractive for uranium recovery applications. A key aspect yet to be explored is how to improve the selectivity and efficiency of COFs for recovering uranium from seawater. To achieve this goal, a series of robust and hydrophilic benzoxazole-based COFs is developed (denoted as Tp-DBD, Bd-DBD, and Hb-DBD) as efficient adsorbents for photo-enhanced targeted uranium recovery. Benefiting from the hydroxyl groups and the formation of benzoxazole rings, the hydrophilic Tp-DBD shows outstanding stability and chemical reduction properties. Meanwhile, the synergistic effect of the hydroxyl groups and the benzoxazole rings in the π-conjugated frameworks significantly decrease the optical band gap, and improve the affinity and capacity to uranium recovery. In seawater, the adsorption capacity of uranium is 19.2× that of vanadium, a main interfering metal in uranium extraction.
科研通智能强力驱动
Strongly Powered by AbleSci AI