Water sorption and dielectric relaxation spectroscopy studies in hydrated Nafion (R) (-SO3K) membranes

Citation
C. Tsonos et al., Water sorption and dielectric relaxation spectroscopy studies in hydrated Nafion (R) (-SO3K) membranes, J MATER SCI, 35(23), 2000, pp. 5957-5965
Citations number
34
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
JOURNAL OF MATERIALS SCIENCE
ISSN journal
00222461 → ACNP
Volume
35
Issue
23
Year of publication
2000
Pages
5957 - 5965
Database
ISI
SICI code
0022-2461(200012)35:23<5957:WSADRS>2.0.ZU;2-3
Abstract
Dynamic and equilibrium sorption isotherm measurements were carried out on hydrated perfluorosulfonate polymer membranes in potassium salt form (Nafio n(R)-SO3K, 1190 EW), at 22 and 40 degreesC respectively. Despite the glassy state of the membrane the diffusion process is Fickian with an average dif fusion coefficient D in the range 2.8-30 x 10(-9) cm(2)/s. The equilibrium sorption isotherms may be quantitatively analyzed according to the GAB equa tion for multilayer sorption processes up to the activity value of alpha = 0.79, which corresponds to 1.0 site-bound water molecules per (-SO3K) group . The analysis of the equilibrium sorption isotherm, using the method of Zi mm and Lundberg, suggests clustering of the water molecules for activities alpha greater than or equal to 0.79. The apparent polymer-water interaction parameter chi.(Flory parameter), was found to have a maximum at alpha = 0. 79 (1.07 < chi less than or equal to 1.95). Also, dielectric relaxation stu dies of the same hydrated Nafion(R) membranes have been carried out in the frequency range of 10(-2) - 5 x 10(6) Hz and in the temperature range of 22 3-295 K. Two relaxation mechanisms were observed which both sift to higher frequencies by increasing the water content. The low frequency relaxation m echanism is due to interfacial polarization which takes place in the hydrat ed ionic regions. The high frequency relaxation mechanism, is a dipolar mec hanism which may be attributed to the rotation of (-SO3-) group-water compl exes at the end of the side chains. (C) 2000 Kluwer Academic Publishers.