Direct hydrogenation of metal carbonate and related salts to methanol, methane and metal hydroxide

Patent metadata

Field	Value
Publication number	US-2025236575-A1
Application number	US-202218703290-A
Country	US
Kind code	A1
Filing date	Sep 28, 2022
Priority date	Oct 21, 2021
Publication date	Jul 24, 2025
Grant date	—

Abstract

A liquid phase process for direct utilization of inorganic metal carbonate and related salts under hydrogenative conditions to produce value-added fuels and feedstocks such as methanol, methane, carbon monoxide, and higher hydrocarbons. Advantageously, the reaction can use heterogeneous catalysts. The hydrogenation proceeds with high selectivity and yield for the desired product at relatively low temperatures, along with co-production of metal hydroxide. The metal hydroxide can be used to capture CO2, forming metal carbonates and bicarbonates that can be reused to produce more methanol and methane, hydrocarbons and carbon monoxide, closing the loop. Such a hydrogenation process can thus also be used in a “carbon capture and recycling” manner to produce renewable methane, methanol, carbon monoxide, hydrocarbons, and other carbon feedstocks from CO2 sourced from any natural and anthropogenic emissions as well as from ambient air.

First claim

What is claimed is:

1 . A method for conversion of a carbonate/formate component comprising:
contacting the carbonate/formate component with hydrogen to produce methanol, methane, carbon monoxide or hydrocarbons or a mixture thereof over a catalyst in a solvent, the catalyst including a transition metal, a post-transition metal, a lanthanide, or combinations thereof.

2 . The method of claim 1 , wherein the catalyst is heterogeneous.

3 . The method of claim 1 , wherein the carbonate/formate component is a metal carbonate, metal bicarbonate, metal formate salt, or mixtures thereof.

4 . The method of claim 1 , wherein a metal hydroxide is produced as a co-product.

5 . The method of claim 1 , wherein the carbonate/formate component is a metal carbonate selected from the group consisting of lithium carbonate, sodium carbonate, potassium carbonate, rubidium carbonate, cesium carbonate, magnesium carbonate, calcium carbonate, strontium carbonate, barium carbonate, and mixtures thereof.

6 . The method of claim 1 , wherein the carbonate/formate component is a metal bicarbonate selected from the group consisting of lithium bicarbonate, sodium bicarbonate, potassium bicarbonate, rubidium bicarbonate, cesium bicarbonate, and mixtures thereof.

7 . The method of claim 1 , wherein the carbonate/formate component is a metal formate salt selected from the group consisting of lithium formate, sodium formate, potassium formate, rubidium formate, cesium formate, and mixtures thereof.

8 . The method of claim 1 , wherein the solvent comprises water, an alcohol, a diol, a polyol or a mixture thereof.

9 . The method of claim 1 , wherein the solvent comprises methanol, ethanol, isopropanol, n-butanol, ethanol propanol, 2-methoxyethanol, ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, polyethylene glycol, propylene glycol, 1,4-butanediol or a mixture thereof.

10 . The method of claim 1 , wherein the carbonate/formate component is a metal carbonate and/or a metal bicarbonate each independently including a component selected from the group consisting of:
naturally occurring minerals; seashells, oyster shells, eggshells; carbonates and bicarbonate salts made by direct CO 2 capture from CO 2 sources using alkali hydroxides and/or amines; synthetic carbonates and bicarbonates; and combinations thereof.

11 . The method of claim 1 , wherein the carbonate/formate component includes naturally occurring minerals are selected from the group consisting of calcite (CaCO 3 ), magnesite (MgCO 3 ), siderite (FeCO 3 ), aragonite (CaCO 3 ), witherite (BaCO 3 ), natrite (Na 2 CO 3 ), ankerite (CaFe—CO 3 ), dolomite (CaMg(CO 3 ) 2 ), huntite (Mg 3 Ca(CO 3 ) 4 ), minrecordite (CaZn(CO 3 ) 2 ), barytocalcite (BaCa(CO 3 ) 2 ), hydromagnesite (Mg 5 (CO 3 ) 4 (OH) 2 ·4H 2 O), ikaite (CaCO 3 ·6(H 2 O)), lansfordite (MgCO 3 ·5(H 2 O)), monohydrocalcite (CaCO 3 ·H 2 O), natron (Na 2 CO 3 ·10(H 2 O)), and combinations thereof.

12 . The method of claim 1 , wherein the hydrogen is produced from a fossil or renewable source.

13 . The method of claim 1 , wherein a heterogeneous catalyst system includes the catalyst.

14 . The method of claim 13 , wherein the heterogeneous catalyst system includes a component selected from the group consisting of copper-based catalysts, indium-based catalysts, nickel-based, indium and nickel/gallium-based catalysts modified with lanthanides and/or precious metals, and combinations thereof.

15 . The method of claim 13 , wherein the heterogeneous catalyst system further includes additional components selected from the group consisting of additives, supports, and combinations thereof.

16 . The method of claim 15 , wherein the additional components are selected from the group consisting of ZnO, ZrO 2 , MOFs, Ga, Al 2 O 3 , SiO 2 . TiO 2 , and combinations thereof.

17 . The method of claim 13 , wherein the heterogeneous catalyst system includes an indium-based species having the formula In 2 O 3 /ZrO 2 .

18 . The method of claim 13 , wherein the heterogeneous catalyst system includes a nickel-based species selected from the group consisting of NiGa/SiO 2 , Ni 3 Ga/SiO 2 , and Ni 5 Ga 3 /SiO 2 .

19 . The method of claim 1 , wherein the catalyst comprises a heterogeneous catalyst based on nickel, cobalt, ruthenium, platinum, palladium, iron, iridium or rhodium and combinations thereof either in their pure form or deposited on a support.

20 . The method of claim 19 , wherein the support is selected from the group consisting of silica, alumina, zirconia, titanium oxide, cerium oxide, silica-alumina, and mixtures thereof.

21 . The method of claim 1 , wherein the catalyst includes a heterogeneous catalyst selected from the group consisting of Fischer-Tropsch type catalysts based on iron, cobalt, and/or ruthenium and catalysts based on iron, copper, molybdenum, cobalt, metal carbides, zeolites or mixtures thereof.

22 . The method of claim 1 , wherein the conversion is conducted at temperatures between 50° C. and 600° C. and gauge pressures between 0 and 200 bar.

23 . The method of claim 1 , wherein the carbonate/formate component is a metal carbonate and/or a metal bicarbonate which is the product of a reaction of a metal hydroxide with CO 2 contained in CO 2 sources.

24 . The method of claim 23 , wherein the CO 2 sources include a CO 2 source selected from the group consisting of fossil fuel power plant flue gases, emissions from industrial and commercial sources, and CO 2 contained in air.

25 . The method of claim 23 , wherein the metal hydroxide comprises lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide, cesium hydroxide, magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide or mixtures thereof.

26 . The method of claim 1 wherein the carbonate/formate component reacts to form a metal hydroxide or a metal hydroxide mixture.

27 . The method of claim 26 , wherein the metal hydroxide or the metal hydroxide mixture is used to capture CO 2 from sources containing between 0.04% and 100% CO 2 , including ambient air, indoor air, industrial flue gases, fossil fuel burning power plants, natural gas purification facilities, cement plants, breweries, biogas, biomass burning facilities and biomass gasification facilities to obtain a metal carbonate, metal bicarbonate or a mixture thereof.

28 . The method of claim 1 , wherein the carbonate/formate component includes a metal carbonate, metal bicarbonate or mixtures thereof, the carbonate/formate component reacting to form a metal hydroxide or metal hydroxide mixture and wherein the metal hydroxide or the metal hydroxide mixture obtained therefrom is used to capture CO 2 from sources containing between 0.04% and 100% CO 2 to obtain the metal carbonate, metal bicarbonate or mixtures thereof and wherein the metal carbonates, metal bicarbonates or mixtures thereof are reusable.

29 . The method of claim 28 , wherein the sources are selected from the group consisting of ambient air, indoor air, industrial flue gases, fossil fuel burning power plants, natural gas purification facilities, cement plants, breweries, biogas, biomass burning facilities and biomass gasification facilities.

30 . The method of claim 1 run either under batch conditions or continuous conditions.

Assignees

• Univ Southern California

Inventors

• Goeppert Alain
• Koch Christopher J
• Prakash G K Surya
• Sen Raktim

Classifications

• C07C2531/12

  containing organo-metallic compounds or metal hydrides · CPC title

• C07C1/12

  from carbon dioxide with hydrogen · CPC title

• C07C2523/755

  Nickel · CPC title

• C07C2523/83

  with rare earths or actinides · CPC title

• C07C1/325

  the hetero-atom being a metal atom · CPC title