Organo-catalytic biomass deconstruction
US-9212104-B2 · Dec 15, 2015 · US
US10647647B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10647647-B2 |
| Application number | US-201716466826-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 4, 2017 |
| Priority date | Dec 7, 2016 |
| Publication date | May 12, 2020 |
| Grant date | May 12, 2020 |
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The invention provides a process for the preparation of ethylene glycol and 1,2-propylene glycol from starting material comprising one or more saccharide, wherein the process comprises the steps of: i) providing the starting material and hydrogen to a first reactor and reacting said starting material and hydrogen therein in the presence of a solvent and a first catalyst system comprising a retro-aldol catalyst composition and a hydrogenation catalyst composition; ii) continuously removing a first reactor product stream from the first reactor, said first reactor product stream comprising ethylene glycol, 1,2-propylene glycol and in the range of from 2 to 40 wt % of sugar alcohols; iii) contacting said first reactor product stream in a second reactor in the presence of hydrogen with a second catalyst system comprising at least a hydrogenation catalyst composition; and iv) converting a portion of the sugar alcohols in the second reactor into ethylene glycol and/or 1,2-propylene glycol to provide a second reactor product stream comprising ethylene glycol, 1,2-propylene glycol and in the range of from 10 to 80% of the amount of sugar alcohols present in the first reactor product stream.
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That which is claimed is: 1. A process for the preparation of ethylene glycol and 1,2-propylene glycol from starting material comprising one or more saccharide, wherein the process comprises the steps of: i) providing the starting material and hydrogen to a first reactor and reacting said starting material and hydrogen therein in the presence of a solvent and a first catalyst system comprising a retro-aldol catalyst composition and a hydrogenation catalyst composition; ii) continuously removing a first reactor product stream from the first reactor, said first reactor product stream comprising ethylene glycol, 1,2-propylene glycol and in the range of from 2 to 40 wt % of sugar alcohols; iii) contacting said first reactor product stream in a second reactor in the presence of hydrogen with a second catalyst system comprising at least a hydrogenation catalyst composition; and iv) converting a portion of the sugar alcohols in the second reactor into ethylene glycol and/or 1,2-propylene glycol to provide a second reactor product stream comprising ethylene glycol, 1,2-propylene glycol and in the range of from 10 to 80% of the amount of sugar alcohols present in the first reactor product stream. 2. The process as claimed in claim 1 , wherein the retro-aldol catalyst composition is homogeneous with respect to the reaction mixture. 3. The process as claimed in claim 1 , wherein the retro-aldol catalyst composition comprises one or more compound, complex or elemental material selected from those containing tungsten. 4. The process as claimed in claim 1 , wherein the first and second hydrogenation catalyst compositions each comprise one or more metals selected from the list consisting of iron, cobalt, nickel, ruthenium, rhodium, palladium, iridium and platinum. 5. The process as claimed in claim 1 , wherein the first reactor product stream comprises in the range of from 5 to 30 wt % of sugar alcohols. 6. The process as claimed in claim 1 , wherein the conditions in the second reactor include one or more of a higher temperature, a lower pressure, a lower hydrogen partial pressure and a lower WHSV than the conditions in the first reactor. 7. The process as claimed in claim 1 , wherein the sugar alcohols remaining in the second reactor product stream are used as a medium for recycling the retro-aldol catalyst composition to the first reactor. 8. The process as claimed in claim 1 , wherein a finishing reactor is used either before, after or both before and after the second reactor and wherein said finishing reactor is operated at a temperature lower than the second reactor.
Sequential processes · CPC title
Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring · CPC title
Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays (synthesis methods per se C40B50/00) · CPC title
Ethylene glycol · CPC title
Tungsten · CPC title
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