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Disclosed is a method of producing hydrogen from oxygenated hydrocarbon reactants, such as glycerol, glucose, or sorbitol. The method can take place in the vapor phase or in the condensed liquid phase. The method includes the steps of reacting water and a water-soluble oxygenated hydrocarbon having

Disclosed is a method of producing hydrogen from oxygenated hydrocarbon reactants, such as glycerol, glucose, or sorbitol. The method can take place in the vapor phase or in the condensed liquid phase. The method includes the steps of reacting water and a water-soluble oxygenated hydrocarbon having at least two carbon atoms, in the presence of a metal-containing catalyst. The catalyst contains a metal selected from the group consisting of Group VIII transitional metals, alloys thereof, and mixtures thereof. The disclosed method can be run at lower temperatures than those used in the conventional steam reforming of alkanes.

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1. A method of producing hydrogen comprising: reacting water and a water-soluble oxygenated hydrocarbon having at least two carbon atoms, at a temperature not greater than about 450° C., in the presence of a metal-containing catalys, and in the absence of added oxygen, wherein the catalyst comprises

1. A method of producing hydrogen comprising: reacting water and a water-soluble oxygenated hydrocarbon having at least two carbon atoms, at a temperature not greater than about 450° C., in the presence of a metal-containing catalys, and in the absence of added oxygen, wherein the catalyst comprises a metal selected am the group consisting of Group VIII transitional metals, alloys thereof, and mixtures thereof.2. The method of claim 1, wherein the water and the oxygenated hydrocarbon are reacted at a temperature of from about 100° C. to about 450° C., and at a pressure where the water and the oxygenated hydrocarbon are gaseous.3. The method of claim 1, wherein the water and the oxygenated hydrocarbon are reacted at a temperature of from about 100° C. to about 300° C., and at a pressure where the water and the oxygenated hydrocarbon are gaseous.4. The method of claim 1, wherein the water and the oxygenated hydrocarbon are reacted at a temperature not greater than about 400° C., at a pressure where the water and the oxygenated hydrocarbon remain condensed liquids.5. The method of claim 1, wherein the water and the oxygenated hydrocarbon are reacted at a pH of from about 4.0 to about 10.0.6. The method of claim 1, wherein the catalyst comprises a metal selected from the group consisting of nickel, palladium, platinum, ruthenium, rhodium, iridium, alloys thereof, and mixtures thereof.7. The method of claim 1, wherein the catalyst is further alloyed or mixed with a metal selected from the group consisting of Group IB metals, Group IIB metals, and Group VIIb metals.8. The method of claim 1, wherein the catalyst is further alloyed or mixed with a metal selected from the group consisting of copper, zinc, and rhenium.9. The method of claim 1, wherein the catalyst is adhered to a support.10. The method of claim 9, wherein the support is selected from the groupconsisting of silica, alumina, zirconia, titania, ceria, carbon, silica-alumina, silica nitride, and boron nitride.11. The method of claim 9, wherein the support is surface-modified to remove surface moieties selected from the group consisting of hydrogen and hydroxyl.12. The method of claim 9, wherein the support is modified by treating it with a modifier selected from the group consisting of silanes, alkali compounds, and alkali earth compounds.13. The method of claim 9, wherein the support is silica modified with trimethylethoxysilane.14. The method of claim 9, wherein the support is a zeolite.15. The method of claim 1, wherein the water and the oxygenated hydrocarbon are reacted at a temperature not greater than about 400° C., and further comprising reacting the water and the water-soluble oxygenated hydrocarbon in the presence of a water-soluble salt of an alkali or alkali earth metal.16. The method of claim 15, wherein the water-soluble salt is selected from the group consisting of an alkali or an alkali earth metal hydroxide, carbonate, nitrate, or chloride salt.17. The method of claim 1, wherein the water-soluble oxygenated hydrocarbon has a carbon-to-oxygen ratio of 1:1.18. The method of claim 1, wherein the water-soluble oxygenated hydrocarbon has from 2 to 12 carbon atoms.19. The method of claim 1, wherein the water-soluble oxygenated hydrocarbon is selected from the group consisting of ethanediol, ethanedione, glycerol, glyceraldehyde, aldotetroses, aldopentoses, aldohexoses, ketotetroses, ketopentoses, ketohexoses, and alditols.20. The method of claim 1, wherein the water-soluble oxygenated hydrocarbon is selected from the group consisting of aldohexoses and corresponding alditols.21. The method of claim 1, wherein the water-soluble oxygenated hydrocarbon is selected from the group consisting of glucose and sorbitol.22. The method of claim 1, wherein the water-soluble oxygenated hydrocarbon is sucrose.23. A method of producing hydrogen comprising: reacting wate and a water-soluble oxygenated hydrocarbon having at least two carbon atoms, at a te perature of from about 100° C. to about 450° C., and at a pressure where the water a d the oxygenated hydrocarbon are gaseous, in the presence of a metal-containing catalyst, and in the absence of added oxygen, wherein the catalyst comprises a metal elected from the group consisting of Group VIII transitional metals, alloys thereof, an mixtures thereof, the catalyst being adhered to a support.24. The method of claim 23, wherein the support is selected from the group consisting of silica, alumina, zirconia, titania, ceria, carbon, silica-alumina, silica nitride, and boron nitride, modified to remove surface moieties selected from the group consisting of hydrogen and hydroxyl.25. The method of claim 24, wherein the support is modified by treating it with a modifier selected from the group consisting of silanes, alkali compounds, and alkali earth compounds.26. The method of claim 23, wherein the support is silica modified with trimethylethoxysilane.27. The method of claim 23, wherein the water-soluble oxygenated hydrocarbon has a carbon-to-oxygen ratio of 1:1.