Author
Listed:
- Lei Mei
(Chinese Academy of Sciences)
- Fei-ze Li
(Chinese Academy of Sciences)
- Jian-hui Lan
(Chinese Academy of Sciences)
- Cong-zhi Wang
(Chinese Academy of Sciences)
- Chao Xu
(Tsinghua University)
- Hao Deng
(Chinese Academy of Sciences)
- Qun-yan Wu
(Chinese Academy of Sciences)
- Kong-qiu Hu
(Chinese Academy of Sciences)
- Lin Wang
(Chinese Academy of Sciences)
- Zhi-fang Chai
(Chinese Academy of Sciences
Chinese Academy of Sciences)
- Jing Chen
(Tsinghua University)
- John K. Gibson
(Lawrence Berkeley National Laboratory)
- Wei-qun Shi
(Chinese Academy of Sciences)
Abstract
Efficient anion recognition is of great significance for radioactive 99TcO4− decontamination, but it remains a challenge for traditional sorbents. Herein, we put forward a tactic using soft crystalline cationic material with anion-adaptive dynamics for 99TcO4− sequestration. A cucurbit[8]uril-based supramolecular metal-organic material is produced through a multi-component assembly strategy and used as a sorbent for effective trapping of TcO4−. Excellent separation of TcO4−/ReO4− is demonstrated by fast removal kinetics, good sorption capacity and high distribution coefficient. Remarkably, the most superior selectivity among metal-organic materials reported so far, together with good hydrolytic stability, indicates potential for efficient TcO4− removal. The structure incorporating ReO4− reveals that the supramolecular framework undergoes adaptive reconstruction facilitating the effective accommodation of TcO4−/ReO4−. The results highlight opportunities for development of soft anion-adaptive sorbents for highly selective anion decontamination.
Suggested Citation
Lei Mei & Fei-ze Li & Jian-hui Lan & Cong-zhi Wang & Chao Xu & Hao Deng & Qun-yan Wu & Kong-qiu Hu & Lin Wang & Zhi-fang Chai & Jing Chen & John K. Gibson & Wei-qun Shi, 2019.
"Anion-adaptive crystalline cationic material for 99TcO4− trapping,"
Nature Communications, Nature, vol. 10(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09504-3
DOI: 10.1038/s41467-019-09504-3
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