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Thermal Polymerization of Styrene Sorbed from the Gas Phase into Polymer Films as a Method for Synthesizing Precursors of Ion-Exchange Membranes

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Abstract—The thermal polymerization of styrene sorbed from the gas-phase into polymer films of polyvinylidene fluoride (PVDF) is carried out at 110°С. By this method, the “matrix‑polystyrene” composites containing up to 70 wt % polystyrene (PS), which serve as precursors of ion-exchange membranes, are synthesized. Sulfonation of grafted PS produces ion-exchange membranes with the exchange capacitance of 1–2.7 mmol/g and the protonic conductivity reaching 20–200 mS/cm when saturated with water at 25°С. The conductivity values indicate that the nonuniformity of PS distribution over film-matrix cross-section usually encountered when monomer sorbed from the gas phase is polymerized does not exert any noticeable effect on the conduction properties of sulfonated composites. The developed method of preparing composites “polymer matrix‑grafted polystyrene” substantially simplifies the synthesis of the precursor of ion-exchange membranes, decreases the necessary amount of reagents, and considerably enhances the safety of synthesis.

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ACKNOWLEDGMENTS

The study was carried out with the use of instruments of the Competence Center on Technologies of New and Mobile Energy Sources at the Institute of Problems of Chemical Physics, Russian Academy of Sciences.

Funding

This study was supported by the Russian Scientific Foundation (project no. 17-79-30054).

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Correspondence to D. A. Kritskaya or K. S. Novikova.

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The authors state the absence of conflict of interest.

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Translated by T. Safonova

Based on the paper presented at the XIV Meeting “Fundamental Problems of Solid State Ionics,” Chernogolovka (Russia), September 9–13, 2018.

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Ponomarev, A.N., Kritskaya, D.A., Abdrashitov, E.F. et al. Thermal Polymerization of Styrene Sorbed from the Gas Phase into Polymer Films as a Method for Synthesizing Precursors of Ion-Exchange Membranes. Russ J Electrochem 55, 738–744 (2019). https://doi.org/10.1134/S1023193519080123

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  • DOI: https://doi.org/10.1134/S1023193519080123

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