海水
堆积
铀
萃取(化学)
化学工程
氢键
比表面积
多孔性
材料科学
氢
化学
有机化学
分子
复合材料
冶金
地质学
工程类
海洋学
催化作用
作者
Ashwini Kaushik,Karan Marvaniya,Y. S. Kulkarni,Dhruv Bhatt,Jahanvi Bhatt,Manoj V. Mane,E. Suresh,Srinu Tothadi,Ketan Patel,S. S. Kushwaha
出处
期刊:Chem
[Elsevier]
日期:2022-10-01
卷期号:8 (10): 2749-2765
被引量:21
标识
DOI:10.1016/j.chempr.2022.07.009
摘要
Uranium extraction from seawater (UES) efficiency is limited by the material design, such as U-selective binding sites, their uniform distribution, surface area exposure, diffusivity, and stability. Herein, we report a U-selective single-component hydrogen-bonded organic framework (CSMCRIHOF-1) of phenoxy-imine synthons conjugated to pyridyl tectons with varied pore dimensions of ∼3.6—∼3.8 Å, resulting in flow-through channels and 328 m2/g BET surface area. The CSMCRIHOF-1 shows a 3D robust network of hydrogen bonds (O−H···O, C−H···O, and O−H···N) supported by π-π stacking, exhibiting excellent hydrolytic stability under broad pH range (pH 1–10). Relative to other framework materials, the CSMCRIHOF-1 is easily processable and regenerable. Further processing of CSMCRIHOF-1 yields large-area free-standing thin films (TFCHs) of tunable thickness from 40 to 500 nm with enhanced surface area (550 m2/g). TFCH shows significant UES capacities of ∼11 mg/g within 5 days and 17.9 mg/g in 30 days from natural seawater.
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