IP Library Granted Patent US 10,367,217
Granted Patent B2
US 10,367,217 · App. 14/616,968 · Granted Jul 30, 2019

Membrane electrode assembly manufacturing process

Inventors: Donald T. Freese (Waikoloa Village, HI); F. Colin Busby (Newark, DE)
Assignee: W. L. Gore & Associates, Inc.
H01M8/1004B32B37/1292C08J5/2237H01M4/8657H01M4/8807H01M4/8828H01M8/106H01M8/1018H01M8/1039H01M8/1053H01M8/1081H01M8/1086B29C65/483B29C66/43B32B27/08B32B27/322B32B2037/243B32B2375/00B32B2457/10B32B2457/18C08J2327/18H01M2008/1095H01M2300/0085Y02P70/56
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Quick Facts
Patent No.
US 10,367,217
App. No.
14/616,968
Granted
Jul 30, 2019
Kind
B2
Abstract

A method of making a component of a membrane electrode assembly comprising the steps of forming an electrode on an air-permeable backer comprising ePTFE, depositing a mixture comprising ionomer and a water-insoluble alcohol onto said electrode, drying said mixture to form a protective ionomer layer, and depositing an ePTFE-reinforced ionomer layer onto said protective ionomer layer.

Claims (38)

1. A method of making a component for a membrane electrode assembly comprising the steps of:

(a) providing an air-permeable backer;

(b) depositing an electrode onto said backer;

(c) depositing an aqueous wet layer comprising a fluoroionomer mixture comprising a water-insoluble alcohol and an ionomer onto said electrode;

(d) substantially drying said wet layer to form a protective ionomer layer; and

(e) depositing, after substantially drying said wet layer, a proton conducting composite wet layer onto said protective ionomer layer, wherein the proton conducting composite wet layer has an occlusive interior volume.

2. A method as defined in claim 1 wherein the air-permeable backer comprises an expanded polymer having release characteristics.

3. A method as defined in claim 2 wherein the expanded polymer is ePTFE.

4. A method as defined in claim 3 wherein said expanded polymer has a mass per area of less than about 16 g/m 2 of ePTFE.

5. A method as defined in claim 3 wherein said expanded polymer has a bubble point of greater than about 70 psi.

6. A method as defined in claim 3 wherein said air-permeable backer has a Z-strength sufficient to prevent cohesive failure of said ePTFE when said electrode is peeled off of said air-permeable backer.

7. A method as defined in claim 1 wherein the air-permeable backer is a gas diffusion layer.

8. A method as defined in claim 1 further comprising coupling a fabric to said backer.

9. A method as defined in claim 8 wherein said air-permeable backer is dimensionally stable within +/−4% throughout the manufacturing process.

10. A method as defined in claim 8 wherein said fabric comprises polyester.

11. A method as defined in claim 8 wherein said fabric has a thickness of less than about 0.006 inches.

12. A method as defined in claim 8 wherein said fabric has a mass/area of less than about 64 g/yd 2 .

13. A method as defined in claim 8 further comprising the step of bonding said fabric to said backer with an adhesive in a discontinuous pattern.

14. A method as defined in claim 13 wherein said fabric is dot-laminated to said backer with a urethane adhesive.

15. A method as defined in claim 13 wherein said adhesive is a solvent-resistant adhesive.

16. A method as defined in claim 1 wherein said ionomer is perfluorosulfonic acid (PFSA) ionomer.

17. A method as defined in claim 1 wherein said wet layer is aqueous and comprises greater than about 60 wt % water.

18. A method as defined in claim 1 wherein said wet layer is aqueous and comprises greater than about 90 wt % water.

19. A method as defined in claim 1 wherein said wet layer is aqueous and comprises less than about 3 wt % of said water-insoluble alcohol.

20. A method as defined in claim 1 wherein said wet layer is aqueous and comprises less than about 5 wt % of said water-insoluble alcohol.

21. A method as defined in claim 1 wherein said water-insoluble alcohol comprises hexanol.

22. A method as defined in claim 1 wherein said wet layer further comprises a water-soluble alcohol.

23. A method as defined in claim 22 wherein said wet layer comprises less than about 10 wt % of said water-soluble alcohol.

24. A method as defined in claim 22 wherein said water-soluble alcohol comprises glycol ether present in an amount of less than about 5 wt %.

25. A method as defined in claim 1 wherein said proton conducting composite wet layer comprises an ionomer.

26. A method as defined in claim 1 wherein said proton conducting composite wet layer comprises a reinforcement.

27. A method as defined in claim 26 wherein said reinforcement comprises an ePTFE membrane.

28. A method as defined in claim 1 further comprising the step of depositing an ionomer layer onto said proton conducting composite wet layer.

29. A method as defined in claim 28 further comprising the step of depositing another electrode onto said ionomer layer.

30. A method as defined in claim 1 further comprising the step of depositing another electrode onto said proton conducting layer.

31. A method as defined in claim 1 wherein said protective ionomer layer has a thickness of about 0.1 to about 25 microns.

32. A method as defined in claim 1 wherein said protective ionomer layer has a thickness of about 0.1 to about 10 microns.

33. A method as defined in claim 1 wherein said protective ionomer layer has a thickness of about 0.1 to about 3 microns.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2015
From: FREESE, DONALD T.; BUSBY, F. COLIN
To: W. L. GORE & ASSOCIATES, INC.
Reel/Frame 035512/0190 →
Continuity (1)
Related Publication 20160233532A1 · Aug 11, 2016