Gram-scale green synthesis of a highly stable cationic covalent organic framework for efficient and selective removal of ReO4/99TcO4

Abstract

Covalent organic frameworks (COFs) have developed as efficient and selective adsorbents to mitigate 99TcO4 contamination. However, the eco-friendly and scalable production of COF-based adsorbents for the removal of 99TcO4 has not yet been reported. This study explores the potential of a cationic COF (TpDB-COF) synthesized via a green hydrothermal method, achieving gram-scale yields per batch, thereby addressing a significant limitation of existing COF production methods. The TpDB-COF demonstrates an exceptional stability in strongly acidic conditions (2 weeks in 3 M HNO3), as well as in various organic solvents, making it suitable for harsh nuclear waste environments. Adsorption experiments using ReO4 as a surrogate for 99TcO4 show rapid adsorption kinetics, reaching nearly 100% removal efficiency within 1 min (with initial concentration of 28 ppm at a solid-to-liquid ratio of 1 g L−1), a maximum adsorption capacity of 570 mg g−1 and excellent stability. Moreover, the COF maintains high selectivity for ReO4 even in the presence of competing anions such as SO42− and NO3. These findings highlight that the hydrothermal synthesis is an effective method to synthesize COF adsorbents for efficient removal of 99TcO4 and offers a sustainable approach for practical applications.

Graphical abstract: Gram-scale green synthesis of a highly stable cationic covalent organic framework for efficient and selective removal of ReO4−/99TcO4−

Supplementary files

Article information

Article type
Paper
Submitted
10 Sep 2024
Accepted
04 Nov 2024
First published
05 Nov 2024
This article is Open Access
Creative Commons BY license

J. Mater. Chem. A, 2024, Advance Article

Gram-scale green synthesis of a highly stable cationic covalent organic framework for efficient and selective removal of ReO4/99TcO4

C. Li, J. Florek, P. Guggenberger and F. Kleitz, J. Mater. Chem. A, 2024, Advance Article , DOI: 10.1039/D4TA06442A

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