Unsupported alkali metal-promoted molybdenum carbide catalysts

Patent metadata

Field	Value
Publication number	US-2026091375-A1
Application number	US-202519335156-A
Country	US
Kind code	A1
Filing date	Sep 22, 2025
Priority date	Sep 30, 2024
Publication date	Apr 2, 2026
Grant date	—

Abstract

An unsupported bulk alkali-promoted molybdenum carbide (A-Mo 2 C) catalyst for use in the reverse water-gas shift (RWGS) reaction, and a method of making the same, is presented. In embodiments, a method for forming an unsupported bulk molybdenum carbide (Mo 2 C) catalyst promoted with an alkali earth metal includes: generating phase pure molybdenum trioxide (MoO 3 ) by calcining a molybdate precursor salt; producing non-passivated Mo 2 C from carburization of the phase pure MoO 3 ; passivating the non-passivated Mo 2 C to form passivated Mo 2 C; and producing an active unsupported alkali metal (A) promoted Mo 2 C (A-Mo 2 C) catalyst from the passivated Mo 2 C and an alkali metal carbonate (A-CO 3 ).

First claim

What is claimed is:

1 . A method of forming an unsupported bulk molybdenum carbide (Mo 2 C) catalyst promoted with an alkali earth metal, the method comprising:
generating phase pure molybdenum trioxide (MoO 3 ) by calcining a molybdate precursor salt; producing non-passivated Mo 2 C from carburization of the phase pure MoO 3 ; passivating the non-passivated Mo 2 C to form passivated Mo 2 C; and producing an active unsupported alkali metal (A) promoted Mo 2 C (A-Mo 2 C) catalyst from the passivated Mo 2 C and an alkali metal carbonate (A-CO 3 ).

2 . The method of claim 1 , wherein the molybdate precursor salt is selected from the group consisting of: ammonium molybdate tetrahydrate ((NH 4 ) 6 Mo 7 O 24 ·4H 2 O), sodium molybdate (Na 2 MoO 4 ), and molybdenum chloride (MoCl 5 ).

3 . The method of claim 1 , wherein the molybdate precursor salt is calcined at a temperature of greater or equal to 600° C. for 12 hours.

4 . The method of claim 1 , wherein a minimum gas hourly space velocity for the carburization is greater or equal to 4.5×10 3 L kg −1 hr −1 .

5 . The method of claim 1 , wherein the carburization occurs for at least 4 hours.

6 . The method of claim 1 , wherein producing the non-passivated Mo 2 C comprises carburizing the phase pure MoO 3 in a flow of methane gas (CH 4 ) and hydrogen gas (H 2 ) for at least 4 hours at a temperature of greater or equal to 600° C.

7 . The method of claim 1 , wherein the alkali metal (A) is selected from the group consisting of: lithium (Li), sodium (Na), potassium (K), and combinations thereof.

8 . The method of claim 1 , wherein the passivating the non-passivated Mo 2 C comprises exposing the non-passivated Mo 2 C to a flow of dioxygen (O 2 ) and nitrogen gas (N 2 ) for 24 hours.

9 . The method of claim 8 , wherein the flow occurs at a total gas hourly space velocity (GHSV) of at least 150 L kg −1 h −1 .

10 . The method of claim 1 , wherein a quantity of the A 2 CO 3 applied is proportional to a total surface area of the passivated Mo 2 C and comprises between 1×10 5 mols A per square meter (mol A m −2 ) and 2.5×10 6 mol A m −2 .

11 . The method of claim 1 , wherein producing the A-Mo 2 C catalyst comprises heating a mixture of the passivated Mo 2 C and an aqueous solution of the alkali metal carbonate (A 2 CO 3 ) at a temperature of 80° C. until evaporation occurs.

12 . The method of claim 1 , further comprising drying the unsupported A-Mo 2 C catalyst to produce a bulk dry powder of the unsupported A-Mo 2 C catalyst.

13 . The method of claim 1 , wherein the unsupported A-Mo 2 C catalyst is selected from the group consisting of: lithium-promoted molybdenum carbide (Li—Mo 2 C), sodium-promoted molybdenum carbide (Na—Mo 2 C), and potassium-promoted molybdenum carbide (K—Mo 2 C).

14 . The method of claim 1 , wherein a molar ratio of the alkali metal (A) to molybdenum (Mo) content in the unsupported A-Mo 2 C catalyst is between 1:2 and 1:8.

15 . The method of claim 14 , wherein the molar ratio of the alkali metal (A) to molybdenum (Mo) content in the A-Mo 2 C catalyst is 1:4.

16 . An active, low temperature Reverse Water-Gas Shift (RWGS) catalyst comprising an unsupported alkali metal (A) promoted molybdenum carbide (A-Mo 2 C) material.

17 . The active RWGS catalyst of claim 16 , wherein the alkali metal (A) is selected from the group consisting of: lithium (Li), sodium (Na), potassium (K), and combinations thereof.

18 . The active RWGS catalyst of claim 16 , wherein a molar ratio of the alkali metal (A) to molybdenum (Mo) content in the A-Mo 2 C catalyst is between 1:2 and 1:8.

19 . The active RWGS catalyst of claim 16 , wherein the RWGS catalyst achieves a CO yield and CO 2 conversion of 38.6% or greater during RWGS at weight hourly space velocities of 3.6×10 5 L kg −1 hr −1 or greater at a temperature of 450° C.

20 . The active RWGS catalyst of claim 16 , wherein the RWGS catalyst achieves a CO yield of 13.5% or greater and a CO 2 conversion of 13.7% or greater at weight hourly space velocities of 18×10 4 L kg −1 hr −1 or greater at a temperature of 300° C.

Assignees

• Us Gov Sec Navy

Inventors

• Morse James R
• Holder Cameron F
• Willauer Heather D
• Baldwin Jeffrey W
• Shabaev Andrew R

Classifications

• B01J37/12

  Oxidising · CPC title

• C10K3/026

  Increasing the carbon monoxide content, e.g. reverse water-gas shift [RWGS] · CPC title

• B01J37/08

  Heat treatment {(B01J37/0009, B01J37/0018 take precedence)} · CPC title

• B01J27/22 Primary

  Carbides · CPC title