Loading…
Sulfonated and crosslinked polyphosphazene-based proton-exchange membranes
Proton-exchange membranes, for possible use in H 2/O 2 and direct methanol fuel cells have been fabricated from poly[bis(3-methylphenoxy)phosphazene] by first sulfonating the base polymer with SO 3 and then solution-casting thin films. The ion-exchange capacity of the membrane was 1.4 mmol/g. Polyme...
Saved in:
Published in: | Journal of membrane science 1999-03, Vol.154 (2), p.175-181 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Proton-exchange membranes, for possible use in H
2/O
2 and direct methanol fuel cells have been fabricated from poly[bis(3-methylphenoxy)phosphazene] by first sulfonating the base polymer with SO
3 and then solution-casting thin films. The ion-exchange capacity of the membrane was 1.4
mmol/g. Polymer crosslinking was carried out by dissolving benzophenone photoinitiator in the membrane casting solution and then exposing the resulting films after solvent evaporation to UV light. The crosslinked membranes look particularly promising for possible proton exchange membrane (PEM) fuel cell applications. A sulfonated and crosslinked polyphosphazene membrane swelled less than Nafion 117 in both water and methanol. Proton conductivities in crosslinked and non-crosslinked 200
μm thick water-equilibrated polyphosphazene films at temperatures between 25°C and 65°C were essentially the same and only 30% lower than those for Nafion 117. Additionally, water and methanol diffusivities in the crosslinked polyphosphazene membrane were very low (≤1.2×10
−7
cm
2/s). Sulfonated/crosslinked polyphosphazene films showed no signs of mechanical failure (softening) up to 173°C and a pressure of 800
kPa and did not degrade chemically when soaked in a hot hydrogen peroxide/ferrous ion solution. |
---|---|
ISSN: | 0376-7388 1873-3123 |
DOI: | 10.1016/S0376-7388(98)00282-8 |