journal article·2013-04

Preparation conditions of inorganic–organic hybrid membranes synthesized from Epoxycyclohexylethyltrimethoxysilane and 1-hydroxyethane-1, 1-diphosphonic acid

Gengjin Kong, Zhihan Guo, Chunhui Shen, Cheng Chen

Publisher page

Abstract

Proton conductive inorganic–organic hybrid membranes were synthesized from Epoxycyclohexylethyltrimethoxysilane (EHTMS) and 1-hydroxyethane-1,1-diphosphonic acid (HEDPA) by the sol–gel method. In this paper, the effect of gel temperature, membrane-forming temperature and Si/P on hybrid membranes performance were discussed. FT-IR studies revealed the phosphonic acid was chemically bonded to the siloxane network. When the membrane-forming temperature is 150 °C, thermal analysis including TG and DTG confirmed that the hybrid membranes were thermally stability up to 250 °C and SEM images showed that the membranes surface smooth and dense, eliminating the phase separation phenomenon. The hybrid membranes with a molar ratio of Si/P = 6/1 possess better thermal stability and preferable flexibility.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Fuel Cells and Related Materials · Conducting polymers and applications · Membrane-based Ion Separation Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (20)

Show source-provided references
1. Li QF, He RH, Jensen JO, Bjerrum NJ (2003) Chem Mater 15:4896–491510.1021/cm0310519 ↗
2. Wieser C et al (2004) Fuel Cells 4:245–25010.1002/fuce.200400038 ↗
3. Hande VR, Rath SK, Rao S, Patri M (2011) J Membrane Sci 372:40–4810.1016/j.memsci.2011.01.042 ↗
4. Xing P, Robertson GP, Guiver MD, Mikhailenko SD, Wang K, Kaliaguine S (2003) J Membrane Sci 229:9510.1016/j.memsci.2003.09.019 ↗
5. Sgreccia E, Di Vona ML, Knauth P (2011) Int J Hydrogen Energy 36:8063–806910.1016/j.ijhydene.2010.11.073 ↗
6. Li X, Zhao C, Lu H, Wang Z, Na H (2005) Polymer 46:5820–582710.1016/j.polymer.2005.04.067 ↗
7. Lins RD, Devanathan R, Dupuis M (2011) J Phys Chem B 115:1817–182410.1021/jp110331m ↗
8. C Wang, DW Shin, SY Lee, N Rae Kang, YM Lee, MD Guiver (2012) J Membrane Sci 405–406:68–7810.1016/j.memsci.2012.02.045 ↗
9. Park KT, Chun JH, Kim SG, Chun BH, Kim SH (2011) Int J Hydrogen Energy 36:1813–181910.1016/j.ijhydene.2010.02.019 ↗
10. Asano N, Aoki M, Suzuki S, Miyatake K, Uchida H, Watanabe M (2006) J Am Chem Soc 128:176210.1021/ja0571491 ↗
11. Schubert U, Husing N, Lorenz A (1995) Chem Mater 7:201010.1021/cm00059a007 ↗
12. Schuster M, Rager T, Noda A, Kreuer KD, Maier J (2005) Fuel Cells 5:355–36510.1002/fuce.200400059 ↗
13. Bock T, Mohwald H, Mulhaupt R (2007) Macromol Chem Phys 208:1324–134010.1002/macp.200700193 ↗
14. Kreuer KD et al (2000) Solid State Ionics 149:136–137
15. Paddison SJ, Kreuer KD, Maier J (2006) Phys Chem Chem Phys 8:4530–454210.1039/b611221h ↗
16. Schuster M, Rager T, Noda A, Kreuer KD, Maier J (2005) Fuel Cells 5:355–36510.1002/fuce.200400059 ↗
17. Wang C, Paddison SJ (2009) Phys Chem Chem Phys 12:970–98110.1039/B917903H ↗
18. Umeda J, Suzuki M, Kato M, Moriya M, Sakamoto W, Yogo T (2010) J Power Sources 195:5882–588810.1016/j.jpowsour.2009.12.078 ↗
19. Umeda J, Moriya M, Sakamoto W, Yogo T (2009) Electrochim Acta 55:298–30410.1016/j.electacta.2009.08.054 ↗
20. Masaki K, Katayama S, Sakamoto W et al (2007) Electrochim Acta 52(19):5924–593110.1016/j.electacta.2007.03.031 ↗