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Strategies for high-temperature methyl iodide capture in azolate-based metal-organic frameworks

Author

Listed:
  • Tingting Pan

    (King Abdullah University of Science and Technology (KAUST))

  • Kaijie Yang

    (King Abdullah University of Science and Technology (KAUST))

  • Xinglong Dong

    (University of Lincoln, Brayford Pool)

  • Shouwei Zuo

    (King Abdullah University of Science and Technology (KAUST))

  • Cailing Chen

    (King Abdullah University of Science and Technology (KAUST))

  • Guanxing Li

    (King Abdullah University of Science and Technology (KAUST))

  • Abdul-Hamid Emwas

    (King Abdullah University of Science and Technology (KAUST))

  • Huabin Zhang

    (King Abdullah University of Science and Technology (KAUST))

  • Yu Han

    (King Abdullah University of Science and Technology (KAUST)
    South China University of Technology
    South China University of Technology)

Abstract

Efficiently capturing radioactive methyl iodide (CH3I), present at low concentrations in the high-temperature off-gas of nuclear facilities, poses a significant challenge. Here we present two strategies for CH3I adsorption at elevated temperatures using a unified azolate-based metal-organic framework, MFU-4l. The primary strategy leverages counter anions in MFU-4l as nucleophiles, engaging in metathesis reactions with CH3I. The results uncover a direct positive correlation between CH3I breakthrough uptakes and the nucleophilicity of the counter anions. Notably, the optimal variant featuring SCN- as the counter anion achieves a CH3I capacity of 0.41 g g−1 at 150 °C under 0.01 bar, surpassing all previously reported adsorbents evaluated under identical conditions. Moreover, this capacity can be easily restored through ion exchange. The secondary strategy incorporates coordinatively unsaturated Cu(I) sites into MFU-4l, enabling non-dissociative chemisorption for CH3I at 150 °C. This modified adsorbent outperforms traditional materials and can be regenerated with polar organic solvents. Beyond achieving a high CH3I adsorption capacity, our study offers profound insights into CH3I capture strategies viable for practically relevant high-temperature scenarios.

Suggested Citation

  • Tingting Pan & Kaijie Yang & Xinglong Dong & Shouwei Zuo & Cailing Chen & Guanxing Li & Abdul-Hamid Emwas & Huabin Zhang & Yu Han, 2024. "Strategies for high-temperature methyl iodide capture in azolate-based metal-organic frameworks," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-47035-8
    DOI: 10.1038/s41467-024-47035-8
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    References listed on IDEAS

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    1. I. Weinrauch & I. Savchenko & D. Denysenko & S. M. Souliou & H-H Kim & M. Le Tacon & L. L. Daemen & Y. Cheng & A. Mavrandonakis & A. J. Ramirez-Cuesta & D. Volkmer & G. Schütz & M. Hirscher & T. Heine, 2017. "Capture of heavy hydrogen isotopes in a metal-organic framework with active Cu(I) sites," Nature Communications, Nature, vol. 8(1), pages 1-7, April.
    2. Baiyan Li & Xinglong Dong & Hao Wang & Dingxuan Ma & Kui Tan & Stephanie Jensen & Benjamin J. Deibert & Joseph Butler & Jeremy Cure & Zhan Shi & Timo Thonhauser & Yves J. Chabal & Yu Han & Jing Li, 2017. "Capture of organic iodides from nuclear waste by metal-organic framework-based molecular traps," Nature Communications, Nature, vol. 8(1), pages 1-9, December.
    3. Kecheng Jie & Yujuan Zhou & Qi Sun & Bo Li & Run Zhao & De-en Jiang & Wei Guo & Hao Chen & Zhenzhen Yang & Feihe Huang & Sheng Dai, 2020. "Mechanochemical synthesis of pillar[5]quinone derived multi-microporous organic polymers for radioactive organic iodide capture and storage," Nature Communications, Nature, vol. 11(1), pages 1-9, December.
    4. Yaqiang Xie & Tingting Pan & Qiong Lei & Cailing Chen & Xinglong Dong & Youyou Yuan & Walid Al Maksoud & Long Zhao & Luigi Cavallo & Ingo Pinnau & Yu Han, 2022. "Efficient and simultaneous capture of iodine and methyl iodide achieved by a covalent organic framework," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
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