Synthesis of copolymer grafts containing sulfoalkyl and hydrophilic groups in polymer electrolyte membranes

Proton exchange type polymer electrolyte membranes (PEM) consisting of ion conducting alkylsulfonic acid and hydrophilic groups such as a hydroxyl group were successfully synthesized by radiation-induced graft polymerization of vinyl acetate (VAc) into a poly(ethylene-co-tetrafluoroethylene) (ETFE) film, followed by saponification and alkylsulfonation with 1,3-propanesulfone. In contrast to the typical S(N)2 reactions in a solution, the base-catalyzed nucleophilic ring-opening reactions of hydroxyl groups of poly(vinylalcohol) grafts with 1,3-propanesultone in solid state ETFE films hardly proceeds in the hydrophilic solvents, but it does proceed in hydrophobic toluene with a weak base (triethylamine) to yield ETFE-grafted poly(vinylalcohol-co-vinylsulfopropyl ether) (PEM-OH) with various values of ion-exchange capacity (IEC) and molar ratio of hydroxyl to sulfo groups in the grafts. The relative-humidity (RH) dependence of the proton conductivity of the sulfonated membrane was compared with that of poly(styrenesulfonic acid)-grafted ETFE (PEM-PSSA) with a similar IEC (similar to 1.3 mmol g(-1)) at 80 degrees C. The PEM-OH showed a conductivity of 1.0 x 10(-3) S cm(-1) under 30% RH, which is higher than those of PEM-PSSA. Further, the PEM-OH with higher IEC (1.9 mmol g(-1)) prepared with a grafting degree of 82% and a sulfonation degree of 41% showed 3.8 x 10(-3) S cm(-1) under 30% RH at 80 degrees C. The conductivity is higher than that of PEMs based on sulfonated polyimide and poly(ether sulfone) with a similar IEC. Furthermore, the tensile strength of PEM-OH was 48 MPa with the elongation at break of 422%, which are better than those of Nafion. These results strongly indicate that the radiation-grafted PEM with hydroxyl groups is a promising material with excellent mechanical and electrochemical properties, which are important characteristics for a fuel cell operating at a high temperature and low humidity. (c) 2012 Elsevier B.V. All rights reserved.