A nitrogen-rich covalent organic framework for simultaneous dynamic capture of iodine and methyl iodide
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Physical Science and Engineering (PSE) Division
Chemical Science Program
Embargo End Date2021-12-01
Permanent link to this recordhttp://hdl.handle.net/10754/666911
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AbstractThe capture of radioiodine species during nuclear fuel reprocessing and nuclear accidents is crucial for nuclear safety, environmental protection, and public health. Previously reported emerging materials for iodine uptake cannot outperform commercial zeolites and active carbon under the practical dynamic scenario. Herein, we present a new design philosophy aiming at significantly enhanced specific host-guest interactions and obtain a nitrogen-rich covalent organic framework material by introducing a bipyridine group into the building block for the simultaneous capture of both iodine gas through enhanced electron-pair effect and organic iodide via the methylation reaction. These efforts give rise to not only an ultrahigh uptake capacity of 6.0 g g−1 for iodine gas and a record-high value of 1.45 g g−1 for methyl iodide under static sorption conditions but also, more importantly, a record-high iodine loading capability under dynamic conditions demonstrated from the breakthrough experiments.
CitationHe, L., Chen, L., Dong, X., Zhang, S., Zhang, M., Dai, X., … Wang, S. (2020). A nitrogen-rich covalent organic framework for simultaneous dynamic capture of iodine and methyl iodide. Chem. doi:10.1016/j.chempr.2020.11.024
SponsorsThis work was supported by grants from the National Natural Science Foundation of China (21825601, 21790374, 21806117, and 21906116) and the National Key R&D Program of China (2018YFB1900203). We thank Prof. Gang Zhou (Hubei University of Technology) as well as Prof. Wei Liu and Prof. Litao Kang (Yantai University) for their support in DFT calculations and Raman measurements, respectively. S.W. conceived and supervised the project; L.H. L.C. and M.Z. performed the synthesis and characterization of the COF material; L.H. X.D. X.L. P.L. and X.L. designed and carried out the static and dynamic adsorption experiments; S.Z. and X.D. performed the computational studies; L.H. F.M. J.C. L.C. and M.Y. carried out the BET analyses and XPS spectra analyses; Y.Z. and C.C. performed the electron microscopy test; T.P. performed the regeneration experiments; S.W. L.H. L.C. Y.H. and X.D. prepared the manuscript. All authors discussed the paper. The authors declare no competing interests.