IP Library Patent Application 13103791
Patent Application
App. No. 13/103,791

LANTHANIDE-MEDIATED PHOTOCHEMICAL WATER SPLITTING PROCESS FOR HYDROGEN AND OXYGEN GENERATION

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Patent No.
US None
App. No.
13/103,791
Abstract

The application generally relates to a process for generating hydrogen, oxygen or both from water. More particularly, the application generally relates to a lanthanide-mediated photochemical process for generating hydrogen, oxygen or both from water.

Claims (66)

1 . A process, comprising:

contacting a metal-solute species with a catalyst, wherein the contacting of the catalyst with the metal-solute species forms molecular oxygen and a reduced form of the metal-solute species.

2 . The process of claim 1 , wherein the metal-solute species comprises one or more of Au 3+ , Pb 2+ , Pb 4+ , Ce 4+ , Pr 4+ , Er 3+ , Bk 4+ , and Cm 4+ .

3 . The process of claim 1 , wherein one or both of the metal-solute species and the reduced form of the metal-solute species comprise a sulfonate and wherein the metal-solute species comprises an aqueous solution.

4 . The process of claim 3 , wherein the sulfonate is selected from sulfate methanesulfonate and a mixture thereof.

5 . The process of claim 1 , wherein the metal-solute species comprises a cerium (IV)-containing sulfonate.

6 . The process of claim 1 , wherein the catalyst is an electron conductor.

7 . The process of claim 1 , wherein the catalyst is selected from the group consisting of a platinum group metal-containing material, activated carbon, carbon nano-tubes and a mixture thereof.

8 . The process of claim 1 , wherein the catalyst is a platinum group metal-containing material and wherein the catalyst has an average surface area from about 10 m 2 /g to about 100 m 2 /g.

9 . The process of claim 1 , wherein the catalyst comprises carbon nano-tubes having surface area greater than about 100 m 2 /g.

10 . The process of claim 9 , wherein the carbon nano-tube catalyst comprises single- or multi-walled nano-tubes.

11 . The process of claim 10 , wherein the carbon nano-tubes have an average tube diameter from about 5 to about 50 nm.

12 . The process of claim 10 , wherein the carbon nano-tubes have an average tube diameter from about 10 to about 30 nm.

13 . The process of claim 1 , wherein the catalyst comprises activated carbon.

14 . The process of claim 13 , wherein the activated carbon comprises a powder having an average surface area greater than about 1,000 m 2 /g.

15 . The process of claim 14 , wherein the activated carbon comprises a powder having an average surface area greater than about 1,500 m 2 /g.

16 . The process of claim 1 , wherein the process is conducted at a temperature of no more than about 50 degrees Celsius.

17 . The process of claim 16 , wherein the process is conducted at a temperature of no more than about 20 degrees Celsius.

18 . The process of claim 1 , wherein the reduced form the metal-solute species comprises one or more of Au + , Pb 2+ , Pb 0 , Ce 3+ , Pr 3+ , Er 2+ , Bk 3+ , and Cm 3+ .

19 . The process of claim 18 , wherein reduced form of the metal-solute species comprises one or both of cerium (III) sulfate and cerium (III) methanesulfonates.

20 . A process, comprising:

applying electromagnetic energy having a wavelength from about 25 nm to about 1000 nm to a metal-solute solution to form molecular hydrogen and an oxidized form of the metal-solute solution, wherein at least some of the electromagnetic energy is absorbed by the metal-solute solution.

21 . The process of claim 21 , wherein the metal-solute species comprises one or more of Au + , Pb 2+ , Pb 0 , Ce 3+ , Pr 3+ , Er 2+ , Bk 3+ and Cm 3+ .

22 . The process of claim 20 , wherein at least one of the metal-solute species comprises and the oxidized form of the metal-solute species comprises a sulfonate and the metal solute solution comprises an aqueous solution.

23 . The process of claim 22 , wherein the metal-solute species comprises one or both of a sulfate and methanesulfonate.

24 . The process of claim 20 , wherein the metal-solute species comprises cerium (III)-containing sulfonate.

25 . The process of claim 24 , wherein the cerium (III)-containing sulfonate comprises sulfuric acid, methanesulfonic acid or a mixture thereof.

26 . The process of claim 20 , wherein the wavelength of the electromagnetic energy is from about 100 to about 325 nm.

27 . The process of claim 20 , wherein a laser provides the electromagnetic energy.

28 . The process of claim 20 , wherein the oxidized form of the metal-solute species comprises one or more of Au 3+ , Pb 2+ , Pb 0 , Ce 4+ , Pr 4+ , Er 3+ , Bk 4+ , and Cm 4+ .

29 . The process of claim 20 , wherein the oxidized form of the metal-solute species comprises one or both of cerium (IV)-containing sulfonate and wherein the cerium (IV)-containing sulfonate comprises one sulfuric acid, methansulfonic acid or a mixture thereof.

30 . A process, comprising:

contacting, in a first compartment, a first metal-solute species with a catalyst, wherein the contacting of the first metal-solute species with the catalyst forms molecular oxygen and a second metal-solute species, wherein the first metal-solute species is an oxidized form of the second metal-solute species;

contacting, in a second compartment containing, a plurality of photons with the second metal-solute species, wherein at least some of the photons are absorbed by the second metal-solute species to form hydrogen gas and the first metal-solute species;

providing the second metal-solute species formed in the first compartment to the second compartment; and

providing the first metal-solute species formed in the second compartment to the first compartment.

31 . The process of claim 30 , wherein first metal-solute species comprises a cerium (IV)-containing sulfonate aqueous solution selected from the group of sulfonates aqueous solutions consisting of sulfate, methanesulfonic acid and a mixture thereof and wherein second metal-solute species comprises a cerium (III)-containing sulfonate selected from the group of sulfonates consisting of sulfate, methanesulfonate and a mixture thereof.

32 . The process of claim 30 , wherein the catalyst is an electron conductor.

33 . The process of claim 30 , wherein the catalyst is selected from the group consisting of a platinum group metal-containing material, activated carbon, carbon nano-tubes, and a mixture thereof.

34 . The process of claim 30 , wherein the catalyst is a platinum group metal-containing material and wherein the catalyst has an average surface area from about 1 m 2 /g to about 200 m 2 /g.

35 . The process of claim 30 , wherein the catalyst comprises carbon nano-tubes and wherein the carbon nano-tubes have an average surface area greater than about 100 m 2 /g.

36 . The process of claim 32 , wherein the carbon nano-tubes comprise single- or multi-walled carbon nano-tubes.

37 . The process of claim 36 , wherein the carbon nano-tubes have an average tube diameter from about 1 to about 50 nm.

38 . The process of claim 36 , wherein the carbon nano-tubes have an average tube diameter from about 10 to about 30 nm.

39 . The process of claim 30 , wherein the catalyst comprises activated carbon.

40 . The process of claim 39 , wherein the activated carbon comprises a powder having an average surface area greater than about 1,000 m 2 /g.

41 . The process of claim 39 , wherein the activated carbon comprises a powder having an average surface area greater than about 1,500 m 2 /g.

42 . The process of claim 30 , further comprising:

separating the catalyst from the molecular oxygen before providing the second metal-solute to the second compartment.

43 . The process of claim 30 , wherein the process is conducted at a temperature no more than about 50 degrees Celsius.

44 . The process of claim 43 , wherein the process is conducted at a temperature no more than about 20 degrees Celsius.

45 . The process of claim 30 , wherein the contacting of the first metal-solute with the catalyst is at a temperature no greater than about 50 degrees Celsius.

46 . The process of claim 45 , wherein the contacting of the first metal-solute with the catalyst is at a temperature no greater than about 20 degrees Celsius.

47 . The process of claim 30 , wherein the plurality of photons have a wavelength from about 25 to about 1,000 nm.

48 . The process of claim 47 , wherein the plurality of photons have a wavelength from about 100 nm to about 400 nm.

49 . The process of claim 47 , wherein the plurality of photons have a wavelength from about 200 to about 300 nm.

50 . The process of claim 30 , further comprising one or both of:

removing the molecular oxygen gas formed in the first compartment from the first compartment; and

removing the molecular hydrogen formed in second compartment from the second compartment.

51 . The process of claim 30 , further comprising:

separating the molecular hydrogen from the second metal-solute species solution before providing the second metal-solute species to the first compartment.

52 . A process, comprising:

contacting, in a first compartment, a cerium (IV)-containing sulfonate aqueous solution with a catalyst, wherein the contacting of the cerium (IV)-containing sulfonate solution with the catalyst forms oxygen gas and cerium (III);

providing, in a second compartment, a plurality of photons having a wavelength from about 200 to about 300 nm to a cerium (III)-containing sulfonate aqueous solution, wherein at least some of the photons are absorbed by the cerium(III)-containing sulfonate solution to form hydrogen gas and cerium (IV);

providing the cerium (III) formed in the first compartment to the second compartment; and

providing the cerium (IV) formed in the second compartment to the first compartment.

Assignments (2)
SECURITY AGREEMENT Recorded Jun 11, 2012
From: MOLYCORP MINERALS, LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 028355/0440 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 26, 2011
From: CABLE, ROBERT; PERROTTA, ANTHONY J.
To: MOLYCORP MINERALS, LLC
Reel/Frame 026344/0233 →