Issue
Korean Journal of Chemical Engineering,
Vol.26, No.2, 518-522, 2009
Synthesis and characterization of poly(ether sulfone) grafted poly(styrene sulfonic acid) for proton conducting membranes
Two-step synthesis of proton-conducting poly(ether sulfone) (PES) graft copolymer electrolyte membrane is proposed. Fridel Craft alkylation reaction was used to introduce chloromethyl pendant group onto the PES polymer backbone. Later on, atom transfer radical polymerization (ATRP) was applied to synthesize a series of poly(ether sulfone) grafted poly(styrene sulfonic acid) (PES-g-PSSA). Successful chloromethyl substitution and grafting of the pendant group was characterized by the 1H-NMR and elemental analysis. Electrochemical properties such as ion exchange capacity (IEC), water uptake and proton conductivity increased with increasing PSSA contents. Thermal gravimetric analysis (TGA) showed the thermal stability of membranes up to 270 ℃. Proton conductivity for maximum amount of grafting was 0.00297 S/cm.
[References]
  1. Chiu CY, Hsu WH, Yen YJ, Kuo SW, Chang FC, Macromolecules, 38(15), 6640, 2005
  2. Kim JH, Kang MS, Kim YJ, Won J, Park NG, Kang YS, Chem. Commun., 14, 1662, 2004
  3. Kim JH, Min BR, Won J, Joo SH, Kim HS, Kang YS, Macromolecules, 36(16), 6183, 2003
  4. Smitha B, Sridhar S, Khan AA, J. Membr. Sci., 225(1-2), 63, 2003
  5. Smitha B, Sridhar S, Khan AA, J. Membr. Sci., 259(1-2), 10, 2005
  6. Di Vona ML, Ahmed Z, Bellitto S, Lenci A, Traversa E, Licoccia S, J. Membr. Sci., 296(1-2), 156, 2007
  7. Licoccia S, Di Vona ML, D'Epifanio A, Ahmed Z, Bellitto S, Marani D, Mecheri B, de Bonis C, Trombetta M, Traversa E, J. Power Sources, 167(1), 79, 2007
  8. Ishikawa K, Kaneko K, Takeoka Y, Rikukawa M, Sanui K, Ito I, Kanzaki Y, Syn. Met., 135, 71, 2003
  9. Bae JM, Honma I, Murata M, Yamamoto T, Rikukawa M, Ogata N, Solid State Ion., 147(1-2), 189, 2002
  10. Neburchilov V, Martin J, Wang HJ, Zhang JJ, J. Power Sources, 169(2), 221, 2007
  11. Ramani V, Kunz HR, Fenton JM, J. Membr. Sci., 266(1-2), 110, 2005
  12. Sambandam S, Ramani V, J. Power Sources, 170(2), 259, 2007
  13. Xing PX, Robertson GP, Guiver MD, Mikhailenko SD, Kaliaguine S, J. Polym. Sci. A: Polym. Chem., 42(12), 2866, 2004
  14. Zschocke P, Quellmalz D, J. Membr. Sci., 22, 325, 1985
  15. Nohay A, Robeson LM, J. Appl Polym. Sci., 20, 1885, 1976
  16. Ueda M, Toyota H, Ochi T, Sugiyama J, Yonetaka K, Masuko T, Teramoto T, J. Polym. Sci., Polym. Chem. Ed., 31, 85, 1993
  17. Wang F, Ji Q, Harrison W, Mecham J, Formato R, Kovar R, Osenar P, McGrath JE, Polym. Preprints, 40, 237, 2000
  18. Im SJ, Patel R, Shin SJ, Kim JH, Min BR, Korean J. Chem. Eng., 25(4), 732, 2008
  19. Ding JF, Chuy C, Holdcroft S, Macromolecules, 35(4), 1348, 2002
  20. Okamura H, Takatori Y, Tsunooka M, Shirai M, Polymer, 43(11), 3155, 2002
  21. Iddon PD, Robinson KL, Armes SP, Polymer, 45(3), 759, 2004
  22. Cho CG, Jang HY, You YG, Li GH, Guk S, High Performance Polymers, 18, 579, 2006
  23. Matyjaszewski K, Xia JH, Chem. Rev., 101(9), 2921, 2001
  24. Avram E, Brebu MA, Warshawsky A, Vasile C, Polymer Degradation and Stability, 69, 175, 2000