Published 2019 | Version v1
Journal article

Ammoniating covalent organic framework (COF) for high‐performance and selective extraction of toxic and radioactive uranium ions

  • 1. State Key Laboratory of Nuclear Resources and Environment, School of Chemistry, Biology and Materials Science, East China University of Technology, Nanchang (China)
  • 2. High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei, Anhui (China)

Description

An ideal porous adsorbent toward uranium with not only large adsorption capacity and high selectivity but also broad applicability even under rigorous conditions is highly desirable but still extremely scarce. In this work, a porous adsorbent, namely [NH4]+[COF‐SO3], prepared by ammoniating a SO3H‐decorated covalent organic framework (COF) enables remarkable performance for uranium extraction. Relative to the pristine SO3H‐decorated COF (COF‐SO3H) with uranium adsorption capacity of 360 mg g1, the ammoniated counterpart of [NH4]+[COF‐SO3] affords ultrahigh uranium uptake up to 851 mg g1, creating a 2.4‐fold enhancement. Such a value is the highest among all reported porous adsorbents for uranium. Most importantly, a large distribution coefficient, KdU, up to 9.8 × 106 mL g1 is observed, implying extremely strong affinity toward uranium. Consequently, [NH4]+[COF‐SO3] affords highly selective adsorption of uranium over a broad range of metal ions such as SU/Cs = 821, SU/Na = 277, and SU/Sr = 124, making it as effective uranium adsorbent from seawater, resulting in amazing uranium adsorption capacity of 17.8 mg g1. Moreover, its excellent chemostability also make it an effective uranium adsorbent even under rigorous conditions (pH = 1, 8, and 3 m acidity). (© 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)

Availability note (English)

Available from: http://dx.doi.org/10.1002/advs.201900547

Additional details

Identifiers

Publishing Information

Journal Title
Advanced Science (Weinheim)
Journal Volume
6
Journal Issue
16
Journal Page Range
p. 1-8
ISSN
2198-3844
CODEN
ASDCCF

Optional Information

Notes
AID: 1900547