Effect of ketone versus sulfone groups on the properties of poly(arylene ether)-based proton exchange membranes
Source abstract
Abstract
A series of sterically encumbered, sulfonated, alternating poly(arylene ether) copolymers were synthesized so as to compare the effects of incorporating ketone and sulfone groups on the proton conductivity and performance of fuel cells of membranes prepared. Therefore, the polymers were prepared by polymerization of 4,4′-difluorobenzophenone or bis(4-fluorophenyl)sulfone with a novel monomer, 2′′,3′′,5′′,6′′-tetraphenyl-[1,1′:4′,1′′:4′′,1′′′:4′′′,1′′′′-quinquephenyl]-4,4′′′′-diol. Subsequent sulfonation and solution casting provided membranes possessing ion exchange capacities ranging from 2.1 to 2.8 mmol g−1. The water uptake of sulfonated polymers increased with increasing IEC, ranging from 68 to 146 % at 80 °C in water compared with 30 % for N117. Proton conductivities ranged between 3 and 17 mS cm−1 at 30 °C/40 % RH, and 88 and 263 mS cm−1 at 80 °C/95 % RH compared with 10 and 100 mS cm−1 for N117, respectively. The proton mobilities ranged between 76.6 × 105 cm2 V−1 S−1 and 170.4 × 105 cm2 V−1 S−1 at 80 °C, greater than that of N117. No substantial difference is observed between membrane prepared from polymers incorporating ketone and analogous membranes incorporating sulfone groups, thus inferring that ketone and sulfone groups in the polymer main chain do not appear to have any discernible difference upon membrane properties.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Fuel Cells and Related Materials · Advanced battery technologies research · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (44)
Show source-provided references
1. Shin DW, Lee SY, Kang NR, Lee KH, Guiver MD, Lee YM (2013) Durable sulfonated poly(arylene sulfide sulfone nitrile)s containing naphthalene units for direct methanol fuel cells (DMFCs). Macromolecules 46(9):3452–346010.1021/ma400154t ↗
2. Stone C, Steck A, Lousenberg RD (1997) Substituted trifluorostyrene compositions. Ballard Power Systems US Paent 5602185
3. Tsang EMW, Zhang Z, Yang ACC, Shi Z, Peckham TJ, Narimani R, Frisken BJ, Holdcroft S (2009) Nanostructure, morphology, and properties of fluorous copolymers bearing ionic grafts. Macromolecules 42(26):9467–948010.1021/ma901740f ↗
4. Mohanty AK, Mistri EA, Ghosh A, Banerjee S (2012) Synthesis and characterization of novel fluorinated poly(arylene ether sulfone)s containing pendant sulfonic acid groups for proton exchange membrane materials. J Membr Sci 409–410:145–15510.1016/j.memsci.2012.03.048 ↗
5. Wang C, Shin DW, Lee SY, Kang NR, Lee YM, Guiver MD (2012) Poly(arylene ether sulfone) proton exchange membranes with flexible acid side chains. J Membr Sci 405–406:68–7810.1016/j.memsci.2012.02.045 ↗
6. Jung MS, Kim TH, Yoon YJ, Kang CG, Yu DM, Lee JY, Kim HJ, Hong YT (2014) Sulfonated poly(arylene sulfone) multiblock copolymers for proton exchange membrane fuel cells. J Membr Sci 459:72–8510.1016/j.memsci.2014.01.072 ↗
7. Feng S, Shen K, Wang Y, Pang J, Jiang Z (2013) Concentrated sulfonated poly(ether sulfone)s as proton exchange membranes. J Power Sources 224:42–4910.1016/j.jpowsour.2012.09.071 ↗
8. Malik RS, Tripathi SN, Gupta D, Choudhary V (2014) Novel anhydrous composite membranes based on sulfonated poly(ether ketone) and aprotic ionic liquids for high temperature polymer electrolyte membranes for fuel cell applications. Int Hydrogen Energy 39(24):12826–1283410.1016/j.ijhydene.2014.06.060 ↗
9. Sohn GJ, Choi HJ, Jeon IY, Chang DW, Dai L, Baek JB (2012) Water-dispersible, sulfonated hyperbranched poly(ether-ketone) grafted multiwalled carbon nanotubes as oxygen reduction catalysts. ACS Nano 6(7):6345–635510.1021/nn301863d ↗
10. Nakagawa T, Nakabayashi K, Higashihara T, Ueda M (2010) A high performance polymer electrolyte membrane based on sulfonated poly(ether sulfone) with binaphthyl units. J Mater Chem 20(32):6662–666710.1039/c0jm00813c ↗
11. Matsumoto K, Nakagawa T, Higashihara T, Ueda M (2009) Sulfonated poly(ether sulfone)s with binaphthyl units as proton exchange membranes for fuel cell application. J Polym Sci Part A 47(21):5827–583410.1002/pola.23627 ↗
12. Wang C, Shin DW, Lee SY, Kang NR, Robertson GP, Lee YM, Guiver MD (2012) A clustered sulfonated poly(ether sulfone) based on a new fluorene-based bisphenol monomer. J Mater Chem 22(48):25093–2510110.1039/c2jm34414a ↗
13. Bae B, Miyatake K, Watanabe M (2010) Sulfonated poly(arylene ether sulfone ketone) multiblock copolymers with highly sulfonated block. Synth Prop Macromol 43(6):2684–269110.1021/ma100291z ↗
14. Rowletta JR, Chena Y, Sgavera AT, Lanea O, Mittelstradt C, Xu H, Zhang M, Moore RB, Mecham S, McGrath JE (2013) Multiblock poly(arylene ether nitrile) disulfonated poly(arylene ether sulfone) copolymers for proton exchange membranes: part 1 synthesis and characterization. Polymer 54(23):6305–631310.1016/j.polymer.2013.09.032 ↗
15. Sakaguchi Y, Takase S, Omote K, Asako Y, Kimura K (2013) Sulfonation of novel fluorine-containing poly(arylene ether nitrile)s for polymer electrolyte membranes. J Macromol Sci, Pure Appl Chem 50(8):879–88410.1080/10601325.2013.802497 ↗
16. Gao Y, Robertson GP, Guiver MD, Jian X, Mikhailenko SD, Wang K, Kaliaguine S (2003) Direct copolymerization of sulfonated poly(phthalazinone arylene ether)s for proton-exchange-membrane materials. J Polym Sci Part A 41(17):2731–274210.1002/pola.10820 ↗
17. Yuan Q, Liu P, Baker GL (2015) Sulfonated polyimide and PVDF based blend proton exchange membranes for fuel cell applications. J Mater Chem A 3(7):3847–385310.1039/C4TA04910A ↗
18. Chen BK, Wu TY, Wong JM, Chang YM, Lee HF, Huang WY, Chen AF (2015) Highly sulfonated diamine synthesized polyimides and protic ionic liquid composite membranes improve PEM conductivity. Polymers 7(6):1046–106510.3390/polym7061046 ↗
19. Kulkarni MP, Peckham TJ, Thomas OD, Holdcroft S (2013) Synthesis of highly sulfonated polybenzimidazoles by direct copolymerization and grafting. J Polym Sci Part A 51(17):3654–366610.1002/pola.26764 ↗
20. Ngamsantivongsa P, Lin HL, Yu TL (2015) Properties and fuel cell applications of polybenzimidazole and ethyl phosphoric acid grafted polybenzimidazole blend membranes. J Membr Sci 491:10–2110.1016/j.memsci.2015.04.045 ↗
21. Lim Y, Lee H, Lee S, Jang H, Hossain MdA, Cho Y, Kim T, Hong Y, Kim W (2014) Synthesis and properties of sulfonated poly(phenylene sulfone)s without ether linkage by diels-alder reaction for PEMFC application. Electrochim Acta 119:16–2310.1016/j.electacta.2013.11.190 ↗
22. Liu B, Robertson GP, Kim DS, Sun X, Jiang Z, Guiver MD (2010) Enhanced thermo-oxidative stability of sulfophenylated poly(ether sulfone)s. Polymer 51(2):403–41310.1016/j.polymer.2009.12.014 ↗
23. Matsumoto K, Higashihara T, Ueda M (2009) Locally sulfonated poly(ether sulfone)s with highly sulfonated units as proton exchange membrane. J Polym Sci Part A 47(13):3444–345310.1002/pola.23403 ↗
24. Shimura T, Miyatake K, Watanabe M (2008) Poly(arylene ether) ionomers containing sulfofluorenyl groups: effect of electron-withdrawing groups on the properties. Eur Polym J 12:4054–406210.1016/j.eurpolymj.2008.09.017 ↗
25. Shang X, Tian S, Kong L, Meng Y (2005) Synthesis and characterization of sulfonated fluorene-containing poly(arylene ether ketone) for proton exchange membrane. J Membr Sci 266(1–2):94–10110.1016/j.memsci.2005.05.014 ↗
26. Wang T, Zhang B, Qiu J, Wu Y, Zhang S, Cao Y (2009) Effects of sulfone/ketone in poly(phthalazinone ether sulfone ketone) on the gas permeation of their derived carbon membranes. J Membr Sci 330(1–2):319–32510.1016/j.memsci.2009.01.006 ↗
27. Lee HF, Wang PH, Huang YC, Su WH, Gopal R, Lee CC, Holdcroft S, Huang WY (2014) Synthesis and proton conductivity of sulfonated, multi-phenylated poly(arylene ether)s. J Polym Sci Part A 52(18):2579–258710.1002/pola.27273 ↗
28. Huang WY, Chang MY, Han YK, Huang PT (2010) Sterically encumbered poly(arylene ether)s containing spiro-annulated substituents: synthesis and thermal properties. J Polym Sci Part A 48(24):5872–588410.1002/pola.24398 ↗
29. Nielsen MM, Yang ACC, Jankova K, Hvilsted S, Holdcroft S (2013) Enhancing the phase segregation and connectivity of hydrophilic channels by blending highly sulfonated graft copolymers with fluorous homopolymers. J Mater Chem A 1(28):8118–812610.1039/c3ta11347g ↗
30. Peckham TJ, Schmeisser J, Rodgers M, Holdcroft S (2007) Main-chain, statistically sulfonated proton exchange membranes: the relationships of acid concentration and proton mobility to water content and their effect upon proton conductivity. J Mater Chem 17(30):3255–326810.1039/b702339a ↗
31. Hickner MA, Ghassemi H, Kim YS, Einsla BR, McGrath JE (2004) Alternative polymer systems for proton exchange membranes (PEMs). Chem Rev 104(10):4587–461210.1021/cr020711a ↗
32. Lee Y, Porter RS (1987) Double-melting behavior of poly(ether ether ketone). Macromolecules 20(6):1336–134110.1021/ma00172a028 ↗
33. Blundell DJ (1987) On the interpretation of multiple melting peaks in poly(ether ether ketone). Polymer 28(13):2248–225110.1016/0032-3861(87)90382-X ↗
34. Coleman JN, Blau WJ, Dalton AB, Muñoz E, Collins S, Kim BG, Razal J, Selvidge M, Vieiro G, Baughman RH (2003) Improving the mechanical properties of single-walled carbon nanotube sheets by intercalation of polymeric adhesives. Appl Phys Lett 82(11):1682–168410.1063/1.1559421 ↗
35. Pang J, Zhang H, Li X, Wang L, Liu B, Jiang Z (2008) Synthesis and characterization of sulfonated poly(arylene ether)s with sulfoalkyl pendant groups for proton exchange membranes. J Membr Sci 318(1–2):271–27910.1016/j.memsci.2008.02.051 ↗
36. Seo DW, Lim YD, Lee SH, Hossain MA, Islam MM, Lee HC, Jang HH, Kim WG (2012) Preparation and characterization of block copolymers containing multi-sulfonated unit for proton exchange membrane fuel cell. Electrochim Acta 86(3):352–359
37. Seo DW, Lim YD, Lee SH, Jeong IS, Kim DI, Lee JH, Kim WG (2012) Preparation and characterization of sulfonated poly(tetra phenyl ether ketone sulfone)s for proton exchange membrane fuel cell. Int Hydrogen Energy 37(7):6140–614710.1016/j.ijhydene.2011.05.168 ↗
38. Li N, Lee SY, Liu YL, Lee YM, Guiver MD (2012) A new class of highly-conducting polymer electrolyte membranes: aromatic ABA triblock copolymers. Energy Environ Sci 5(1):5346–535510.1039/C1EE02556B ↗
39. Jang H, Islam MM, Lim Y, Lee S, Hossain MA, Hong T, Lee S, Hong Y, Kim WG (2014) Synthesis and characterization of sulfonated cardo based poly(arylene ether sulfone) multiblock copolymers for proton exchange membrane. Solid State Ionics 262:845–85110.1016/j.ssi.2013.09.037 ↗
40. Miyatake K, Chikashige Y, Higuchi E, Watanabe M (2007) Tuned polymer electrolyte membranes based on aromatic polyethers for fuel cell applications. J Am Chem Soc 129(13):3879–388710.1021/ja0672526 ↗
41. Mauritz KA, Moore RB (2004) State of understanding of nafion. Chem Rev 104(10):4535–458510.1021/cr0207123 ↗
42. Li L, Chung DDL (1994) Electrical and mechanical properties of electrically conductive polyethersulfone composites. Composites 25(3):215–22410.1016/0010-4361(94)90019-1 ↗
43. Sandler J, Werner P, Shaffer MSP, Demchuk V, Altstädt V, Windle AH (2002) Carbon-nanofibre-reinforced poly(ether ether ketone) composites. Compos A 33(8):1033–103910.1016/S1359-835X(02)00084-2 ↗
44. Li G, Xie J, Cai H, Qiao J (2014) New highly proton-conducting membrane based on sulfonated poly(arylene ether sulfone)s containing fluorophenyl pendant groups, for low-temperature polymer electrolyte membrane fuel cells. Int Hydrogen Energy 39(6):2639–264810.1016/j.ijhydene.2013.11.049 ↗