A novel graft copolymer consisting of a poly(vinylidene fluoride‐co‐chlorotrifluoroethylene) backbone and poly(glycidyl methacrylate) side chains, that is, P(VDF‐co‐CTFE)‐g‐PGMA, was synthesized through atom transfer radical polymerization (ATRP) using CTFE units as a macroinitiator. Successful synthesis and microphase‐separated structure of the polymer were confirmed by 1H NMR, FTIR spectroscopy, and TEM. As‐synthesized P(VDF‐co‐CTFE)‐g‐PGMA copolymer was sulfonated by sodium bisulfite, followed by thermal crosslinking with sulfosuccinic acid (SA) via the esterification to produce grafted/crosslinked polymer electrolyte membranes. The IEC values continuously increased with increasing SA content but water uptake increased with SA content up to 10 wt %, above which it decreased again as a result of competitive effect between crosslinking and hydrophilicity of membranes. At 20 wt % of SA content, the proton conductivity reached 0.057 and 0.11 S/cm at 20 and 80 °C, respectively. The grafted/crosslinked P(VDF‐co‐CTFE)‐g‐PGMA/SA membranes exhibited good mechanical properties (>400 MPa of Young's modulus) and high thermal stability (up to 300 °C), as determined by a universal testing machine (UTM) and TGA, respectively.
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Roh et al. (2010) studied this question.
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