Method for the production of glycols from an anhydrosugar feed
US-2019194100-A1 · Jun 27, 2019 · US
US11078138B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11078138-B2 |
| Application number | US-201916968154-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 29, 2019 |
| Priority date | Feb 9, 2018 |
| Publication date | Aug 3, 2021 |
| Grant date | Aug 3, 2021 |
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A hydrogenolysis process is disclosed for directly converting a sugar feed comprised of a high fructose feedstock, a high sucrose feedstock, or a combination of these to a mixed lower polyols product including both propylene glycol and ethylene glycol. The process provides greater propylene glycol selectivity than ethylene glycol selectivity such that the propylene glycol is present to a greater extent than the ethylene glycol in the mixed lower polyols product. The sugar feed and a source of hydrogen are supplied to a reaction vessel and reacted in the presence of a hydrogenolysis catalyst comprising molybdenum (Mo) and ruthenium (Ru).
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The invention claimed is: 1. A process for directly converting a sugar feed comprised of fructose, dextrose or sucrose to a mixed lower polyols product including both propylene glycol and ethylene glycol, comprising supplying the sugar feed and a source of hydrogen to a reaction vessel and reacting the sugar feed and hydrogen in the presence of a hydrogenolysis catalyst comprising Mo and Ru to provide propylene glycol preferentially to ethylene glycol in the mixed lower polyols product. 2. The process of claim 1 , wherein the Mo is present at 0.5 to 10% by weight of the sugar feed. 3. The process of claim 1 or claim 2 , wherein the Ru is present at 3-7% by weight of the hydrogenolysis catalyst. 4. The process of claim 1 , wherein the hydrogenolysis catalyst comprises a support material. 5. The process of claim 4 , wherein the support material comprises carbon. 6. The process of claim 4 , wherein the support material is selected from the group consisting of a carbon based support material, activated carbon, zirconium oxide, titanium oxide, niobium oxide, tin oxide, lanthanum oxide, tungsten oxide, silicon carbide, silicon oxycarbide, titanium carbide, titanium oxycarbide, zirconium oxycarbide, tungsten carbide, tungsten oxycarbide, and combination of any thereof. 7. The process of claim 6 , wherein the Mo is present at about 9-10% by weight of the sugar feed. 8. The process of claim 7 , wherein the Ru is present at about 5% by weight of the hydrogenolysis catalyst. 9. The process of claim 8 , wherein the Mo is in the form of molybdate. 10. The process of claim 9 , wherein the Mo is in the form of potassium molybdate. 11. The process of claim 10 , wherein the Mo is in the form of potassium molybdate in the range of 3-10% by weight of the sugar feed. 12. The process of claim 1 , wherein the sugar feed is placed in contact with the catalyst at a liquid hourly space velocity of between velocity of 0.2 hr −1 to 2 hr −1 . 13. The process of claim 12 , further comprising maintaining a reaction temperature of between 180 to 250 degrees C. 14. The process of claim 13 , further comprising maintaining a hydrogen pressure of 600 to 2500 psi. 15. The process of claim 14 , wherein the reaction vessel is a sealed hydrogenolysis reactor, and the process is conducted for a period of time in the range of 1 hour to 10 hours. 16. The process of claim 14 , wherein the sugar feed is an aqueous fructose solution. 17. The process of claim 14 , wherein the sugar feed is an aqueous sucrose solution. 18. The process of claim 14 , wherein the sugar feed is an aqueous dextrose solution.
using catalysts, e.g. selective catalysts · CPC title
by reduction of an oxygen containing functional group · CPC title
of a —CHO group · CPC title
Molybdenum · CPC title
Tungsten · CPC title
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