Method for preparing an enhanced proton exchange membrane and enhanced proton exchange membrane

Patent metadata

Field	Value
Publication number	US-8951694-B2
Application number	US-201013147060-A
Country	US
Kind code	B2
Filing date	Feb 1, 2010
Priority date	Feb 5, 2009
Publication date	Feb 10, 2015
Grant date	Feb 10, 2015

Abstract

A novel approach based on the increase of the intrinsic oxidative stability of uncrosslinked membranes is addressed. The co-grafting of styrene with methacrylonitrile (MAN), which possesses a protected α-position and strong dipolar pendant nitrile group, onto 25 μm ETFE base film is disclosed. Styrene/MAN co-grafted membranes were compared to styrene based membrane in durability tests in single H 2 /O 2 fuel cells. The incorporation of MAN improves the chemical stability dramatically. The membrane preparation based on the copolymerization of styrene and MAN shows encouraging results and offers the opportunity of tuning the MAN and crosslinker content to enhance the oxidative stability of the resulting fuel cell membranes.

First claim

The invention claimed is:

1. A method of preparing a membrane to be assembled in a membrane electrode assembly, the method which comprises:
a) irradiating a base polymer film with radiation selected from the group consisting of electromagnetic radiation and particle radiation in order to form reactive centers (i.e. radicals) within the base polymer film;
b) exposing the irradiated base polymer film to a mixture of monomers amenable to radiation-induced graft polymerization comprising styrene and methacrylonitrile to induce a formation of a graft copolymer in the irradiated base polymer film and to form a grafted base polymer film; and
c) sulfonating the grafted base polymer film to introduce sulfonic acid sites providing ionic conductivity of the material.

2. The method according to claim 1 , which comprises assembling the membrane in a polymer electrolyte membrane fuel cell.

3. The method according to claim 1 , which comprises setting a ratio of styrene to methacrylonitrile within a range from 10:90 to 90:10.

4. The method according to claim 3 , which comprises setting the ratio to substantially 50:50.

5. The method according to claim 3 , which comprises setting the ratio to substantially 1/2.

6. The method according to claim 1 , wherein the mixture comprises 5 to 20 vol % styrene and 5 to 20 vol % methacrylonitrile.

7. The method according to claim 6 , wherein the mixture contains further monomers, or a solvent, or a solvent mixture.

8. The method according to claim 7 , wherein the further monomers include a crosslinker.

9. The method according to claim 8 , wherein the crosslinker is selected from the group consisting of DVB, DIPB, and BVPE.

10. The method according to claim 6 , wherein the mixture contains isopropanol and water.

11. The method according to claim 6 , wherein the mixture comprises 10 to 40 vol % monomers, 50 to 90 vol % isopropanol, and 5 to 20 vol % water.

12. The method according to claim 1 , wherein step b) is carried out under an inert atmosphere over a period of at least one hour.

Assignees

• Ben-Youcef Hicham
• Gubler Lorenz
• Henkensmeier Dirk
• Scherrer Inst Paul

Inventors

• Ben-Youcef Hicham
• Gubler Lorenz
• Henkensmeier Dirk

Classifications

• H01M8/1039

  halogenated, e.g. sulfonated polyvinylidene fluorides · CPC title

• C08J2333/20

  Homopolymers or copolymers of acrylonitrile (C08J2355/02 takes precedence) · CPC title

• H01M8/1023

  having only carbon, e.g. polyarylenes, polystyrenes or polybutadiene-styrenes · CPC title

• C08J5/2243 Primary

  obtained by introduction of active groups capable of ion-exchange into compounds of the type C08J5/2231 · CPC title

• H01M8/0289

  Means for holding the electrolyte (solid polymer electrolytes H01M8/1018) · CPC title