IP Library Granted Patent US 7,871,955
Granted Patent B2
US 7,871,955 · App. 11/088,343 · Granted Jan 18, 2011

Platinum catalysts from in situ formed platinum dioxide

Assignee: BASF Fuel Cell GmbH
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Quick Facts
Patent No.
US 7,871,955
App. No.
11/088,343
Granted
Jan 18, 2011
Kind
B2
Abstract

A carbon-supported platinum catalyst obtained by chemical reduction of in situ-formed platinum dioxide on a carbon support and a method of production thereof.

Claims (18)

1. A method for the production of a carbon-supported platinum catalyst comprising:

(i) formation of platinum dioxide on a carbon support in an aqueous solution, said platinum dioxide being in situ-formed from of dihydrogen-hexahydroxyplatinate in an acidic solution by variation of the pH between 2 and 5 and/or temperature between 30 and 100° C. and said carbon support slurried in a non-complexing strong acid,

(ii) chemically reducing in situ-formed platinum dioxide on a carbon support in an aqueous solution, with a reducing agent selected from the group consisting of formaldehyde, formic acid, oxalic acid, sodium borohydride and hypophosphite

(iii) performing a thermal treatment in a controlled atmosphere between 120 and 500° C.

2. The method of claim 1 wherein said in situ formation of platinum dioxide is obtained by converting a dihydrogen hexahydroxyplatinate precursor pre-adsorbed on said carbon support.

3. The method of claim 1 wherein said variation of pH is obtained by the addition of caustic soda or ammonia.

4. The method of claim 3 wherein said addition of caustic soda or ammonia is effected up to a pH between 2 and 5.

5. The method of claim 1 wherein said variation of temperature consists of bringing said aqueous solution from room temperature to a final temperature of 30 to 100° C.

6. The method of claim 1 wherein said carbon support is a carbon black having an active area not lower than 50 m 2 /g.

7. The method of claim 6 wherein said carbon black is slurried in a strong acid selected from the group consisting of HNO 3 , HC 1 O 4 , CF 3 COOH, toluenesulfonic acid, trifluoromethanesulfonic acid, HCl, HBr, prior to the adsorption of said dihydrogen hexahydroxyplatinate precursor.

8. The method of claim 7 wherein said variation of pH is obtained by the addition of caustic soda or ammonia.

9. The method of claim 8 wherein said addition of caustic soda or ammonia is effected up to a pH between 2 and 5.

10. The method of claim 1 wherein said controlled atmosphere is a reducing atmosphere or an inert atmosphere.

11. A method for the production of a platinum black catalyst comprising chemically reducing platinum dioxide formed in situ by conversion of dihydrogen-hexahydroxyplatinate from an acidic solution by variation of the pH between 2 and 5 and/or temperature between 30 and 100° C.

12. The method of claim 11 wherein said variation of temperature consists of bringing said aqueous solution from room temperature to a final temperature of 30 to 100° C.

13. A method for the production of a carbon-supported platinum catalyst comprising:

(i) formation of platinum dioxide on a carbon support in an aqueous solution, said platinum dioxide being in situ-formed from of dihydrogen-hexahydroxyplatinate in an acidic solution by variation of the pH between 2 and 5 and/or temperature between 30 and 100° C. and said carbon support slurried in a non-complexing strong acid,

(ii) chemically reducing in situ-formed platinum dioxide on a carbon support in a reducing agent selected from the group consisting of hydrogen gas during a thermal treatment in a controlled atmosphere between 120 and 500° C.

Assignments (3)
CHANGE OF NAME Recorded Jul 11, 2008
From: PEMEAS GMBH
To: BASF FUEL CELL GMBH
Reel/Frame 021281/0446 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2008
From: DE NORA ELETTRODI S.P.A.
To: PEMEAS GMBH
Reel/Frame 020339/0836 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2005
From: CAO, LIXIN; TSOU, YU-MIN; CASTRO, EMORY DE; MARTELLI, GIAN NICOLA
To: DE NORA ELETTRODI S.P.A.
Reel/Frame 016419/0651 →
Continuity (2)
Provisional Application 6056120700 · Apr 9, 2004
Related Publication 20050227862A1 · Oct 13, 2005