Methods of producing hydrogen-selective oxygen carrier materials

Patent metadata

Field	Value
Publication number	US-11794181-B2
Application number	US-201917271093-A
Country	US
Kind code	B2
Filing date	Aug 27, 2019
Priority date	Aug 31, 2018
Publication date	Oct 24, 2023
Grant date	Oct 24, 2023

Abstract

Embodiments of the present disclosure are directed to methods of producing a hydrogen-selective oxygen carrier material comprising combining one or more core material precursors and one or more shell material precursors to from a precursor mixture and heat-treating the precursor mixture at a treatment temperature to form the hydrogen-selective oxygen carrier material. The treatment temperature is greater than or equal to 100° C. less than the melting point of a shell material, and the hydrogen-selective oxygen carrier material comprises a core comprising a core material and a shell comprising the shell material. The shell material may be in direct contact with at least a majority of an outer surface of the core material.

First claim

The invention claimed is:

1. A method of producing a hydrogen-selective oxygen carrier material, the method comprising:
combining one or more core material precursors, one or more shell material precursors, and one or more support materials to form a precursor mixture; and
heat-treating the precursor mixture at a treatment temperature to form the hydrogen-selective oxygen carrier material, wherein the treatment temperature is greater than or equal to 100° C. less than the melting point of a shell material; and
wherein the hydrogen-selective oxygen carrier material comprises a core comprising a core material and a shell comprising the shell material, wherein the shell material is in direct contact with at least a majority of an outer surface of the core material, and wherein the shell material comprises one or more alkali transition metal oxides comprising:
one or more of Na, Li, K, or Cs; and
one or more of W, or Mo wherein the one or more core material precursors are formed prior to combining the one or more core material precursors and the one or more shell material precursors, and wherein the one or more core material precursors comprises two or more transition metal oxides.

2. The method of claim 1 , wherein the one or more core material precursors consists of a single core material precursor and the one or more shell material precursors consists of a single shell material precursor.

3. The method of claim 1 , further comprising forming the one or more shell material precursors prior to combining the one or more core material precursors and one or more shell material precursors.

4. The method of claim 1 , wherein the precursor mixture comprises at least two shell material precursors, and wherein the at least two shell material precursors react to form the shell material during the heat-treating.

5. The method of claim 1 , wherein the one or more core material precursors and the one or more shell material precursors are combined in a solution to form the precursor mixture.

6. The method of claim 1 , wherein the combining of the one or more core material precursors and the one or more shell material precursors comprises physically mixing the one or more core material precursors in a dry powder state with the one or more shell material precursors in a dry powder state.

7. The method of claim 1 , further comprising drying the precursor mixture prior to the heat-treating.

8. The method of claim 1 , wherein the heat-treating is at a temperature of less than the melting point of the core material.

9. The method of claim 1 , wherein the precursor mixture is heat treated for about 0.5 hours to about 12 hours.

10. The method of claim 1 , wherein the core material comprises a redox-active transition metal oxide.

11. The method of claim 1 , further comprising combining the one or more core material precursors the one or more support materials separately before combining the one or more shell material precursors.

12. The method of claim 10 , wherein the redox-active transition metal oxide is chosen from Mn 2 O 3 , Fe 2 O 3 , CO 3 O 4 , CuO, (LaSr)CoO 3 , (LaSr)MnO 3 , Mg 6 MnO 8 , MgMnO 3 , MnO 2 , Fe 3 O 4 , Mn 3 O 4 , or Cu 2 O.

Assignees

• Dow Global Technologies Llc

Inventors

• Sharma Manish
• Goodfellow Brian W
• Yancey David F
• Malek Andrzej
• Stangland Eric E

Classifications

• C01G45/125

  of the type (MnO3)n-, e.g. CaMnO3 · CPC title

• C01G45/1221

  Manganates or manganites with trivalent manganese, tetravalent manganese or mixtures thereof · CPC title

• B01J2523/00

  Constitutive chemical elements of heterogeneous catalysts · CPC title

• B02C17/24

  Driving mechanisms · CPC title

• C01B3/26

  using catalysts · CPC title