Abstract
In order to achieve effective removal of radioactive iodine, trace detection of dinitrophenol (DNP), here, we have synthesized two porous organic polymers (POPs, TMCHA and HMCHA) by nucleophilic substitution reactions with specific surface areas of 1730 and 1796 m2 g−1, respectively. The adsorption capacities of POPs in iodine vapor and cyclohexane and the fluorescence sensing performances for DNP are studied. The results show that the adsorption capacities of TMCHA and HMCHA in iodine vapor are as high as 3.77 and 2.74 g g−1, and the removal efficiencies of iodine in iodine-cyclohexane solution are 97% and 73%, respectively. The iodine adsorption mechanism of the MCHA-based POPs is the electron transfer mechanism. The Stern–Volmer quenching constants (Ksv) of TMCHA and HMCHA for fluorescence quenching of DNP are 4.04 × 103 and 4.42 × 103 L mol−1, respectively. The fluorescence quenching of TMCHA and HMCHA was caused by FRET and PET together.
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Acknowledgements
This work was supported by the Open Fund of Anhui Province Key Laboratory of Optoelectronic and Magnetism Functional Materials (under Grant No. ZD2021001).
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The Open Fund of Anhui Province Key Laboratory of Optoelectronic and Magnetism Functional Materials, ZD2021001, Tongmou Geng.
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Xia Zhang: Data curation; investigation; software; writing – original draft; Conceptualization. Yachen Wang: Data curation; investigation; software. Tongmou Geng: Data curation; investigation; software; funding aquisition; supervision, writing-review and editing.
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Zhang, X., Wang, Y. & Geng, T. The synthesis of 4,4'-methylenebis(cyclohexylamine)-based porous organic polymers via nucleophilic substitution reactions for uptaking iodine and fluorescence sensing to dinitrophenol. J Polym Res 31, 106 (2024). https://doi.org/10.1007/s10965-024-03920-w
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DOI: https://doi.org/10.1007/s10965-024-03920-w