Catalysts for hydrodeoxygenation of oxygenated hydrocarbons

Patent metadata

Field	Value
Publication number	US-10131604-B2
Application number	US-201314419395-A
Country	US
Kind code	B2
Filing date	Aug 15, 2013
Priority date	Aug 15, 2012
Publication date	Nov 20, 2018
Grant date	Nov 20, 2018

Abstract

The present invention provides catalysts, methods, and reactor systems for converting oxygenated hydrocarbons to oxygenated compounds. The invention includes methods for producing cyclic ethers, monooxygenates, dioxygenates, ketones, aldehydes, carboxylic acids, and alcohols from oxygenated hydrocarbons, such as carbohydrates, sugars, sugar alcohols, sugar degradation products, and the like, using catalysts containing Group VIII metals. The oxygenated compounds produced are useful in the production of liquid fuels, chemicals, and other products.

First claim

The invention claimed is:

1. A heterogeneous catalyst for producing a reaction product, the heterogeneous catalyst comprising (i) palladium, (ii) tin, (iii) molybdenum, and (iv) a carbon support or a hydrothermally stable metal oxide support selected from the group consisting of zirconia, titania, silica-alumina, theta alumina, and mixtures thereof,
wherein the heterogeneous catalyst is stable when present during an aqueous reaction between hydrogen and an oxygenated hydrocarbon selected from the group consisting of a starch, a sugar, a sugar alcohol, a polysaccharide, an oligosaccharide, a trisaccharide, a disaccharide, a monosaccharide, and combinations thereof, at a reaction temperature between about 100° C. and about 300° C. and a reaction pressure between about 70 psig and about 2000 psig;
wherein the heterogeneous catalyst is capable of producing the reaction product for greater than 20 days; and
wherein the reaction product is selected from the group consisting of a cyclic ether, a polyol, a ketone, an aldehyde, a carboxylic acid, an alcohol, and combinations thereof.

2. The heterogeneous catalyst of claim 1 , wherein the heterogeneous catalyst comprises between 0.05 and 5.0 wt % palladium and between 0.0125 to 5.0 wt % tin.

3. The heterogeneous catalyst of claim 1 , wherein the heterogeneous catalyst comprises between 0.05 and 10.0 wt % molybdenum.

4. The heterogeneous catalyst of claim 1 , wherein the metal oxide support is an acidic support.

5. The heterogeneous catalyst of claim 1 , wherein the metal oxide support is modified with a modifier selected from the group consisting of tungsten, titania, sulfate, phosphate, and silica.

6. The heterogeneous catalyst of claim 1 , wherein the metal oxide support is selected from the group consisting of tungstated zirconia, titania zirconia, sulfated zirconia, phosphated zirconia, and mixtures thereof.

7. A method for converting oxygenated hydrocarbons to alcohols and cyclic ethers, the method comprising:
contacting an aqueous oxygenated hydrocarbon feedstock and hydrogen with the heterogeneous catalyst of claim 1 to produce a mixture of reaction products, the mixture comprising alcohols having a concentration greater than about 1% as a weight percentage of the total carbon entering the system and cyclic ethers having a concentration greater than about 1% as a weight percentage of the total carbon entering the system.

8. The method of claim 7 , wherein the aqueous oxygenated hydrocarbon feedstock comprises water and one or more oxygenated hydrocarbons selected from the group consisting of a starch, a sugar, a sugar alcohol, a polysaccharide, an oligosaccharide, a trisaccharide, a disaccharide, a monosaccharide, a polyhydric alcohol, a sugar degradation product, lignin, phenolics, and methoxy-substituted phenolics.

9. The method of claim 7 , wherein the reaction product further comprises one or more oxygenates selected from the group consisting of a polyol, a ketone, an aldehyde, a carboxylic acid, and an alcohol.

10. The method of claim 7 , wherein the oxygenated hydrocarbon feedstock is contacted with the heterogeneous catalyst at a reaction temperature between 100° C. and 300° C.

11. The method of claim 7 , wherein the oxygenated hydrocarbon feedstock is contacted with the heterogeneous catalyst at the reaction pressure between 70 psig and 2000 psig.

12. The method of claim 7 , wherein the oxygenated hydrocarbon feedstock is contacted with the heterogeneous catalyst at a weight hour space velocity of 0.01 to 10.0 grams of soluble oxygenated hydrocarbon per gram of heterogeneous catalyst per hour.

13. The method of claim 7 , the method further comprising catalytically reacting a portion of the reaction product with a condensation catalyst to produce C 4+ compounds selected from the group consisting of a C 4+ alcohol, a C 4+ ketone, a C 4+ alkane, a C 4+ alkene, a C 5+ cycloalkane, a C 5+ cycloalkene, an aryl, and a fused aryl.

14. The method of claim 13 , wherein the C 4+ compounds comprise an aryl selected from the group consisting of toluene, orthoxylene, metaxylene, paraxylene, ethylbenzene, and combinations thereof.

15. The method of claim 13 , the method further comprising C 4+ compounds are distilled to provide a composition selected from the group consisting of an aromatic fraction, a gasoline fraction, a kerosene fraction, and a diesel fraction.

16. The method of claim 7 , wherein the refractive index of the aqueous phase reaction products is greater than a threshold value for a period of greater than about 20 days without a regeneration of the catalyst.

17. The method of claim 7 , wherein the refractive index of the aqueous phase reaction products does not vary more than about 1% from the mean over a period of about 20 days without a regeneration of the catalyst.

Assignees

• Virent Inc

Inventors

• Blank Brian
• Cortright Randy
• Beck Taylor
• Woods Elizabeth
• Jehring Michael

Classifications

• B01J38/12

  Treating with free oxygen-containing gas · CPC title

• C07C41/18 Primary

  by reactions not forming ether-oxygen bonds · CPC title

• B01J23/6567

  Rhenium · CPC title

• B01J2523/17

  Copper · CPC title

• B01J2523/51

  Phosphorus · CPC title