Ethanol Production via Dimethylether Recycle
US-2017022129-A1 · Jan 26, 2017 · US
US11352309B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11352309-B2 |
| Application number | US-202117237232-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 22, 2021 |
| Priority date | Mar 8, 2017 |
| Publication date | Jun 7, 2022 |
| Grant date | Jun 7, 2022 |
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Provided is a catalyst including a metal component including a first component that is rhenium and one or more second components selected from the group consisting of silicon, gallium, germanium, and indium and a carrier on which the metal component is supported, the carrier including an oxide of a metal belonging to Group 4 of the periodic table. Also provided is an alcohol production method in which a carbonyl compound is treated using the above catalyst. It is possible to produce an alcohol by a hydrogenation reaction of a carbonyl compound with high selectivity and high efficiency while reducing side reactions.
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The invention claimed is: 1. An alcohol production method in which an alcohol is produced from a carbonyl compound, the method comprising producing an alcohol by contacting a carbonyl compound with a catalyst, the catalyst comprising a metal component comprising a first component that is rhenium and one or more second components selected from the group consisting of silicon, gallium, germanium, and indium, and a carrier on which the metal component is supported, a mass ratio of elements that are the second components to the rhenium element being in a range of 0.1 to 10. 2. The alcohol production method according to claim 1 , wherein the second components of the catalyst comprise germanium. 3. The alcohol production method according to claim 1 , wherein the metal component further comprises a third component, which is a metallic element belonging to Groups 8 to 10 of the periodic table, the metallic element being other than iron or nickel, wherein a mass ratio of the metallic element to the rhenium element included in the catalyst is less than 0.2. 4. The alcohol production method according to claim 3 , wherein the metallic element comprises ruthenium. 5. The alcohol production method according to claim 1 , wherein the carrier is a carbonaceous carrier or a carrier comprising an oxide of a metal belonging to Group 4 of the periodic table. 6. The alcohol production method according to claim 1 , wherein the catalyst is a catalyst prepared by a method comprising attaching the metal component to a carrier comprising a sulfate ion. 7. The alcohol production method according to claim 6 , wherein the sulfate ion content in the carrier is 0.01% by mass to 10% by mass of the mass of the carrier. 8. The alcohol production method according to claim 6 , wherein the sulfate ion content in the catalyst is 0.01% by mass to 10% by mass of the mass of the catalyst. 9. The alcohol production method according to claim 1 , wherein a sulfate ion content in the catalyst is 0.01% by mass to 10% by mass of the mass of the catalyst. 10. A method of hydrogenating a carbonyl compound to a corresponding alcohol, the method comprising: producing the corresponding alcohol by contacting the carbonyl compound with a catalyst, the catalyst comprising a metal component comprising a first component that is rhenium and one or more second components selected from the group consisting of silicon, gallium, germanium, and indium, and a carrier on which the metal component is supported, a mass ratio of elements that are the second components to the rhenium element being in a range of 0.1 to 10. 11. The method according to claim 10 , wherein the carbonyl compound is at least one selected from the group consisting of a carboxylic acid, a carboxylic acid ester, a carboxylic anhydride, and an aldehyde. 12. The method according to claim 10 , wherein the carbonyl compound is a polyvalent carboxylic acid, and the corresponding alcohol is a hydroxycarboxylic acid or a polyhydric alcohol. 13. The method according to claim 10 , wherein carrier comprises titanium oxide and/or zirconium oxide. 14. The method according to claim 10 , wherein the catalyst is prepared by a method comprising attaching the metal component to the carrier, wherein the carrier further comprises a sulfate ion. 15. The method according to claim 14 , wherein the sulfate ion content in the carrier is 0.01% by mass to 10% by mass of the mass of the carrier. 16. The method according to claim 14 , wherein the sulfate ion content in the catalyst is 0.01% by mass to 10% by mass of the mass of the catalyst. 17. The method according to claim 10 , wherein the method provides a molar ratio of a defunctionalized by-product to the corresponding alcohol of less than 0.060. 18. The method according to claim 17 , wherein the molar ratio of the defunctionalized by-product to the corresponding alcohol is from 0.004 to 0.039.
using catalysts, e.g. selective catalysts · CPC title
Rhenium · CPC title
Titanium; Oxides or hydroxides thereof · CPC title
Zirconium or hafnium; Oxides or hydroxides thereof · CPC title
Rhenium · CPC title
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