铀酰
材料科学
离子
吸附
铀
水溶液中的金属离子
选择性
铵
无机化学
化学工程
金属
物理化学
化学
有机化学
冶金
催化作用
工程类
作者
Doudou Cao,Fengchao Cui,Cheng Zhang,Yajie Yang,Jiarui Cao,Yingbo Song,Yuebing Zheng,Liping Wen,Xiangyu Kong,Hongjuan Ma,Shusen Chen,Yan Song,Fengju Wang,Guangshan Zhu,Ye Yuan
标识
DOI:10.1002/adma.202500567
摘要
Abstract Biomimetic nanochannels enable fast and selective transport of mononuclear metal ions; however, their construction for complex ion transport remains in its infancy due to the nonuniform charge distribution and large geometric dimensions of coordination compounds. Herein, an ionic electrostatic interaction template strategy is proposed to prepare biomimetic channels for the capture of complex ions. Using the [UO 2 (CO 3 ) 3 ] 4− ion as a template, various quaternary ammonium monomers with lengths of 6.2−8.4 Å are decorated on 1D porous channels of the TpBDOH framework via the Williamson ether reaction. Accordingly, the pore size is modulated in the sub‐nanometer range of 9−13 Å, facilitating multiple electrostatic attractions between quaternary ammonium fragments and the three equatorial carbonate ions on the [UO 2 (CO 3 ) 3 ] 4− ion. The unique structure enabled highly efficient uranium adsorption with a capacity of 501.5 mg g −1 and a high selectivity coefficient for uranium over vanadium of >163.1. The resulting electropositive nanochannels selectively captured [UO 2 (CO 3 ) 3 ] 4− ions from natural seawater, achieving a high uptake of 25.3 mg g −1 in 35 days.
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