4.6 Article

Rational construction of covalent organic frameworks with multi-site functional groups for highly efficient removal of low-concentration U(vi) from water

Journal

ENVIRONMENTAL SCIENCE-NANO
Volume 8, Issue 5, Pages 1469-1480

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1en00059d

Keywords

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Funding

  1. National Key Research and Development Program of China [2019YFA0210401]
  2. National Natural Science Foundation of China [21836002, 21906059]
  3. Guangdong Science and Technology Program [2020B121201003]
  4. Guangdong Innovative and Entrepreneurial Research Team Program [2016ZT06N569]

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The study developed a novel COF material with multiple capture sites for efficient adsorption of low-concentration uranium in water, demonstrating a high affinity towards uranium and effective removal efficiency exceeding 99.2%. The mechanism studies revealed that the chelation interaction between multi-site amidoxime groups and uranium played a key role in enhancing the adsorption affinity.
Uranium, a key nuclide in the nuclear industry, has substantially damaged the ecological environment and human health due to its high toxicity and radioactivity. Therefore, its efficient separation and extraction from water are of great significance for environmental safety. However, the low concentration of uranium in water requires capture materials with high adsorption affinity, which poses a severe challenge to conventional materials. Herein, we designed a novel covalent organic framework (COF-TpDd-AO(2)) with two amidoxime groups in each structure unit, to provide multiple capture sites towards uranium, as the trap material. This COF exhibited different adsorption behaviors towards uranium with different concentrations, with a maximum affinity of 8.27 x 10(5) mL g(-1), which was 6.82 and 9.81 times higher than those of the control sample COF-TpDb-AO with a single amidoxime group and the pristine COF-TpDd. The removal efficiency exceeded 99.2% with the initial uranium concentration of 0.5 mg L-1. Mechanism studies showed that the chelation interaction between multi-site amidoxime groups and uranium acted as the dominant adsorption force. Moreover, with the increasing density of the amidoxime group in COF-TpDd-AO(2), the chelation effect changed from one single site to multiple sites, thus further enhancing the uranium affinity. This work suggested that the purposeful design of COFs with multi-site amidoxime groups could be an effective strategy to improve the adsorption affinity of COFs towards low-concentration uranium.

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