IP Library Granted Patent US 7,824,788
Granted Patent B2
US 7,824,788 · App. 11/375,605 · Granted Nov 2, 2010

CCM composite

Assignee: Solvay Solexis S.p.A.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,824,788
App. No.
11/375,605
Granted
Nov 2, 2010
Kind
B2
Abstract

CCM formed of a membrane having on one of the two surfaces a first electrocatalytic layer containing a catalyst and on the other one a second electrocatalytic layer containing a catalyst, said electrocatalytic layers and said membrane containing (per)fluorinated ionomers, said CCM having the following characteristics: size variations, for both the orthogonal directions of the plane xy, lower than 15%, by dipping the CCM, after drying at 105° C. under vacuum for one hour in demineralized water at 100° C. for 30 minutes; the CCM remains substantially unchanged after having been subjected to treatments of 60 cycles by dipping in water at 80° C. for 8 hours and then in water at the temperature of 25° C. for 16 hours.

Claims (41)

1. A catalyst coated membrane (CCM) comprising a membrane having on one of the two surfaces a first electrocatalytic layer comprising a catalyst and on the other one a second electrocatalytic layer comprising a catalyst, wherein:

the orthogonal projection of the perimeter of the first electrocatalytic layer on the second layer is distant from the perimeter of the second electrocatalytic layer at least 1 mm in each point of said projection;

both the electrocatalytic layers and the membrane, comprise (per)fluorinated ionomers, and wherein the CCM has the following features:

size variations in the orthogonal directions of the plane xy lower than 15% after CCM dipping in demineralized water at 100° C. for 30 minutes, dried at 105° C. under vacuum for one hour;

the electrocatalytic layers of the CCM remain adherent to the membrane after 60 cycles by dipping in water at 80° C. for 8 hours and then in water at the temperature of 25° C. for 16 hours.

2. A CCM according to claim 1 , wherein the (per)fluorinated ionomers are sulphonic ionomers having an equivalent weight in the range from 380 to 1,700 g/eq.

3. A CCM according to claim 1 , wherein the (per)fluorinated ionomers comprise the following units:

copolymers comprising:

(A) monomeric units deriving from one or more fluorinated monomers comprising at least one ethylenic unsaturation;

(B) fluorinated monomeric units comprising sulphonyl —SO 2 F groups in amounts such that the ionomer has the equivalent weight in the above range;

homopolymers formed of monomeric units (B); subsequent ionomer hydrolysis to convert the —SO 2 F groups into sulphonic groups in acid —SO 3 H or salified form.

4. A CCM according to claim 3 , wherein the fluorinated monomers (A) are selected from the following:

vinylidene fluoride (VDF);

C 2 -C 8 perfluoroolefins;

C 2 -C 8 chloro- and/or bromo- and/or iodo-fluoroolefins;

CF 2 ═CFOR fl (per) fluoroalkylvinylethers (PAVE), wherein R fl is a C 1 -C 6 (per) fluoroalkyl;

CF 2 ═CFOX perfluoro-oxyalkylvinylethers, wherein X is a C 1 -C 12 perfluoro-oxyalkyl having one or more ether groups.

5. A CCM according to claim 3 , wherein the fluorinated monomers (B) are selected from one or more of the following:

F 2 C═CF—O—CF 2 —CF 2 —SO 2 F;

F 2 C═CF—O—[CF 2 —CX A F—O] nA —(CF 2 ) nB —SO 2 F wherein X A ═Cl, F or CF 3 ; nA=1-10, nB=2,3;

F 2 C═CF—O—CF 2 —CF 2 —CF 2 —SO 2 F;

F 2 C═CF—Ar—SO 2 F wherein Ar is an aryl ring.

6. A CCM according to claim 3 , wherein the sulphonic (per)fluorinated ionomers further comprise from 0.01% to 2% by moles of monomeric units deriving from a bis-olefin of formula:

R 1 R 2 C═CH—(CF 2 ) m —CH═CR 5 R 6   (I)

wherein:

m=2-10;

R 1 , R 2 , R 5 , R 6 , equal to or different from each other, are H or C 1 -C 5 alkyl groups.

7. A CCM according to claim 3 , wherein the (per)fluorinated ionomers comprise, optionally in admixture with the monomers with —SO 2 F groups, monomers comprising precursor groups which by hydrolysis are transformed into —COOH groups, selected from the following:

F 2 C═CF—O—CF 2 —CF 2 —Y;

F 2 C═CF—O—[CF 2 —CX A F—O] nA —(CF 2 ) nB —Y

wherein X A ═C1, F or CF 3 ; nA=1-10, nB=2,3;

F 2 C═CF—O—CF 2 —CF 2 —CF 2 —Y;

F 2 C═CF—Ar—Y wherein Ar is an aryl group;

wherein Y is a precursor group of the carboxylic group, selected from the following: CN, COF, COOH, COOR B , COO − Me + , CONR 2B R 3B , wherein R B is C 1 -C 10 and R 2B and R 3B , equal or different, are H or have the meaning of R B , Me is an alkaline metal.

8. A CCM according to claim 3 , wherein the membrane and the electrocatalytic layers comprise (per)fluorinated ionomers obtained from ionomers comprising:

monomeric units deriving from TFE;

monomeric units deriving from CF 2 ═CF—O—CF 2 CF 2 SO 2 F.

9. A CCM according to claim 1 , wherein the electrocatalytic layers comprise an ionomer and a catalyst selected between Pt or a mixture of Pt with one or more metals optionally supported on carbon.

10. A CCM according to claim 1 , wherein the ratio by weight between catalyst and ionomer in each of the two electrocatalytic layers ranges from 0.5 to 4.

11. A CCM according to claim 9 , wherein the ratio mg of catalyst metal/cm 2 of electrocatalytic layer ranges from 0.01 to 2.

12. A CCM according to claim 11 , wherein the ratio (weight in mg of catalyst metal)/(cm 2 of electrocatalytic layer), when hydrogen is used as fuel, ranges from 0.01 to 0.7 mg/cm 2 , when methanol is used it ranges from 0.3 to 1 mg/cm 2 at the anode side and from 0.5 to 2 mg/cm 2 at the cathode side.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2006
From: ARCELLA, VINCENZO; GHIELMI, ALESSANDRO; VACCARONO, PAOLA; MERLO, LUCA
To: SOLVAY SOLEXIS S.P.A.
Reel/Frame 017751/0279 →
Priority Claims (1)
IT M12005A0446 · Mar 17, 2005 · national
Continuity (1)
Related Publication 20060216564A1 · Sep 28, 2006