Sulfonated Polybenzothiazoles: A Novel Candidate for Proton Exchange Membranes
Source abstract
Abstract
Sulfonated polybenzothiazoles (sPBT) with high molecular weight as well as excellent solubility were synthesized for the first time, which was achieved by attaching the phenylsulfonyl pendant groups or incorporating the hexafluoroisopropylidene moieties to the polymer backbone. Such sulfonated polybenzothiazoles thus could be cast into homogeneous membranes and could be further evaluated as proton exchange membranes. These sPBTs showed high thermal stability and high proton conductivity as well as low swelling. For instance, the hexafluoroisopropylidene-containing sPBT with a disulfonation degree of 65% exhibited a T d5 of 380 °C, a proton conductivity of 0.11 S/cm, and a swelling of 15.5% at 80 °C. In addition, the sPBT membranes showed excellent oxidative and hydrolytic stability. In comparison with the phenylsulfonyl pendant-group-containing sPBT membranes, the hexafluoroisopropylidene-containing sPBT membranes with an equivalent ion exchange capacity showed much narrower ionic channels because of the hydrophobic hexafluoroisopropylidene moieties. This made the latter display better dimensional stability, oxidative stability, and hydrolytic stability than the former. This investigation illustrated that sulfonated polybenzothiazoles are a novel candidate for proton exchange membranes.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Fuel Cells and Related Materials · Membrane-based Ion Separation Techniques · Electrocatalysts for Energy Conversion
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry and Chemical Engineering, The State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P. R. China
References (67)
Show source-provided references
1. Hickner M. A. · Chem. Rev. · 2004 · 104 · 458710.1021/cr020711a ↗
2. Li Q. F. · Chem. Mater. · 2003 · 15 · 489610.1021/cm0310519 ↗
3. Kreuer K. D. · J. Membr. Sci. · 2001 · 185 · 2910.1016/S0376-7388(00)00632-3 ↗
4. Savadogo O. · J. Power Sources · 2004 · 127 · 13510.1016/j.jpowsour.2003.09.043 ↗
5. Kerres J. A. · J. Membr. Sci. · 2001 · 185 · 310.1016/S0376-7388(00)00631-1 ↗
6. Jones D. J. · Adv. Polym. Sci. · 2008 · 215 · 219
7. Alberti G. · Annu. Rev. Mater. Res. · 2003 · 33 · 12910.1146/annurev.matsci.33.022702.154702 ↗
8. Jones D. J. · J. Membr. Sci. · 2001 · 185 · 4110.1016/S0376-7388(00)00633-5 ↗
9. Kim Y. S. · J. Polym. Sci., Part B: Polym. Phys. · 2003 · 41 · 281610.1002/polb.10496 ↗
10. Wang Z. · J. Membr. Sci. · 2006 · 285 · 23910.1016/j.memsci.2006.08.038 ↗
11. Lee C. H. · J. Membr. Sci. · 2007 · 303 · 25810.1016/j.memsci.2007.07.026 ↗
12. Bai Z. W. · Macromol. Rapid Commun. · 2006 · 27 · 127110.1002/marc.200600275 ↗
13. Lee J. K. · J. Membr. Sci. · 2007 · 294 · 7510.1016/j.memsci.2007.02.013 ↗
14. Ma X. H. · J. Membr. Sci. · 2008 · 310 · 30310.1016/j.memsci.2007.11.003 ↗
15. Matsumura S. · Macromolecules · 2008 · 41 · 27710.1021/ma071423p ↗
16. Xiao G. Y. · Polymer · 2002 · 43 · 533510.1016/S0032-3861(02)00365-8 ↗
17. Zhu X. L. · J. Membr. Sci. · 2008 · 312 · 5910.1016/j.memsci.2007.12.058 ↗
18. Gao Y. · Polymer · 2006 · 47 · 80810.1016/j.polymer.2005.12.015 ↗
19. Asano N. · Chem. Mater. · 2004 · 16 · 284110.1021/cm049550c ↗
20. Marestin C. · Adv. Polym. Sci. · 2008 · 216 · 185
21. Guo X. X. · Macromolecules · 2002 · 35 · 670710.1021/ma020260w ↗
22. Li N. W. · J. Polym. Sci., Part A: Polym. Chem. · 2008 · 46 · 282010.1002/pola.22616 ↗
23. Wycisk R. · Adv. Polym. Sci. · 2008 · 216 · 157
24. Allcock H. R. · J. Polym. Sci., Part B: Polym. Phys. · 2006 · 44 · 235810.1002/polb.20864 ↗
25. Yang H. H. · 1989
26. Hu X. D. · Macromol. Mater. Eng. · 2003 · 288 · 82310.1002/mame.200300013 ↗
27. So Y. H. · Prog. Polym. Sci. · 2000 · 25 · 13710.1016/S0079-6700(99)00038-6 ↗
28. Wainright J. S. · J. Electrochem. Soc. · 1995 · 142 · L12110.1149/1.2044337 ↗
29. Qing S. B. · React. Funct. Polym. · 2006 · 66 · 21910.1016/j.reactfunctpolym.2005.07.020 ↗
30. Kawahara M. · Electrochim. Acta · 2000 · 45 · 139510.1016/S0013-4686(99)00349-7 ↗
31. Mader J. · Adv. Polym. Sci. · 2008 · 216 · 63
32. Peron J. · J. Membr. Sci. · 2008 · 314 · 24710.1016/j.memsci.2008.01.044 ↗
33. Staiti P. · J. Membr. Sci. · 2001 · 188 · 7110.1016/S0376-7388(01)00359-3 ↗
34. Jannasch P. · Fuel Cells · 2005 · 5 · 24810.1002/fuce.200400051 ↗
35. Asensio J. A. · J. Polym. Sci., Part A: Polym. Chem. · 2002 · 40 · 370310.1002/pola.10451 ↗
36. Li Q. F. · Chem. Mater. · 2007 · 19 · 35010.1021/cm0627793 ↗
37. Sakaguchi Y. · Polym. Mater. Sci. Eng. · 2001 · 84 · 899
38. Einsla B. R. · Abstr. Pap. Am. Chem. Soc. · 2003 · 226 · U391
39. Tan N. · Polym. Bull. · 2009 · 62 · 59310.1007/s00289-009-0042-2 ↗
40. Hwang W. F. · Polym. Eng. Sci. · 1983 · 23 · 78410.1002/pen.760231407 ↗
41. Hattori T. · Macromolecules · 1992 · 25 · 335110.1021/ma00039a005 ↗
42. Baek J. B. · Macromolecules · 2008 · 41 · 119610.1021/ma071757e ↗
43. Park S. -Y. · Polymer · 2004 · 45 · 4910.1016/j.polymer.2003.10.033 ↗
44. Hutzler R. F. · High Perform. Polym. · 1992 · 4 · 16110.1088/0954-0083/4/3/004 ↗
45. Kricheldorf H. · Makromol. Chem. · 1990 · 191 · 201710.1002/macp.1990.021910904 ↗
46. Evers R. C. · Macromolecules · 1981 · 14 · 92510.1021/ma50005a007 ↗
47. Saegusa Y. · J. Polym. Sci., Part A: Polym. Chem. · 1998 · 36 · 42910.1002/(SICI)1099-0518(199802)36:3<429::AID-POLA7>3.0.CO;2-M ↗
48. Reynolds J. R. · Polym. Prep. · 1993 · 34 · 1065
49. Kim S. · J. Polym. Sci., Part A: Polym. Chem. · 1996 · 34 · 48110.1002/(SICI)1099-0518(199602)34:3<481::AID-POLA17>3.0.CO;2-L ↗
50. Dang T. D. · Polym. Prep. · 2003 · 44 · 927
51. Qing S. B. · J. Polym. Sci., Part A: Polym. Chem. · 2005 · 43 · 436310.1002/pola.20842 ↗
52. Hodson, H. F.; Batchelor, J. F.U.S. Patent 4 103 015, 1978.
53. Bennett O. F. · Can. J. Chem. · 1965 · 43 · 188010.1139/v65-247 ↗
54. Holt G. · J. Chem. Soc. · 1960 · 250810.1039/jr9600002508 ↗
55. Asano N. · J. Am. Chem. Soc. · 2006 · 128 · 176210.1021/ja0571491 ↗
56. Li W. M. · J. Membr. Sci. · 2008 · 315 · 17210.1016/j.memsci.2008.02.026 ↗
57. Chow A. W. · Macromolecules · 1989 · 22 · 351410.1021/ma00199a002 ↗
58. Osaheni J. A. · Chem. Mater. · 1992 · 4 · 128210.1021/cm00024a031 ↗
59. Kim D. S. · J. Polym. Sci., Part A: Polym. Chem. · 2008 · 46 · 98910.1002/pola.22442 ↗
60. Xing P. X. · Polymer · 2005 · 46 · 325710.1016/j.polymer.2005.03.003 ↗
61. Ding J. F. · Macromolecules · 2002 · 35 · 134810.1021/ma010970m ↗
62. Tian S. H. · Macromolecules · 2009 · 42 · 115310.1021/ma802456m ↗
63. Xing P. · Macromolecules · 2004 · 37 · 796010.1021/ma0494941 ↗
64. Chikashige Y. · Macromolecules · 2005 · 38 · 712110.1021/ma050856u ↗
65. Lee K. S. · Macromolecules · 2009 · 42 · 58410.1021/ma802233j ↗
66. Zhang C. J. · J. Membr. Sci. · 2009 · 329 · 9910.1016/j.memsci.2008.12.021 ↗
67. Wang F. · J. Membr. Sci. · 2002 · 197 · 23110.1016/S0376-7388(01)00620-2 ↗