Chemical recyling of plastics using ionic liquids or deep eutectic solvents
US-2024052133-A1 · Feb 15, 2024 · US
US2016017381A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016017381-A1 |
| Application number | US-201514804161-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 20, 2015 |
| Priority date | Jul 18, 2014 |
| Publication date | Jan 21, 2016 |
| Grant date | — |
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This disclosure relates to compositions and methods for converting biomass to various chemical intermediates and final products including fuels. Aspects include the depolymerization of lignin, cellulose, and hemicellulose to a wide slate of depolymerization compounds that can be subsequently metabolized by genetically modified bacterium, and converted to cis,cis-muconic acid. Other aspects include the use of monometallic catalysts for converting the cis,cis-muconic acid to commodity chemicals and fuels, for example adipic acid and/or nylon.
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What is claimed is: 1 . A genetically modified microorganism comprising at least one exogenous gene addition, wherein the at least one added gene encodes at least one of a decarboxylase, a dehydratase, or a monooxygenase. 2 . The microorganism of claim 1 , further comprising at least one endogenous gene deletion, wherein the at least one deleted gene encodes at least one of a dioxygenase, a muconate lactonizing enzyme, or muconolactone isomerase. 3 . The microorganism of claim 1 , wherein the microorganism over-expresses at least one demethylase gene. 4 . The microorganism of claim 1 , further comprising a deletion of at least one catabolite repression control gene of the microorganism. 5 . The microorganism of claim 1 , wherein the at least one exogenous gene encodes a decarboxylase from Enterobacter cloacae. 6 . The microorganism of claim 5 , wherein the exogenous gene is at least one of aroY, ecdB, or ecdD. 7 . The microorganism of claim 1 , wherein the at least one exogenous gene encodes a dehydratase from Bacillus cereus. 8 . The microorganism of claim 7 , wherein the exogenous gene is at least one of aroZ or asbF. 9 . The microorganism of claim 1 , wherein the at least one exogenous gene encodes a monooxygenase from Pseudomonas sp. CF600. 10 . The microorganism of claim 9 , wherein the exogenous gene is at least one of dmpK, dmpL, dmpM, dmpN, dmpO, dmpP, or pheA. 11 . The microorganism of claim 2 , wherein the at least one deleted gene is at least one of pcaH or pcaG. 12 . The microorganism of claim 2 , wherein the at least one deleted gene is at least one of catB or catC. 13 . The microorganism of claim 3 , wherein the demethylase gene is at least one of vanA, vanB, or ligM. 14 . The microorganism of claim 1 , wherein the microorganism is at least one of a bacterium, a fungus, a yeast, a prokaryote, or a prokaryotic microorganism. 15 . The microorganism of claim 14 , wherein the microorganism is a prokaryote or prokaryotic microorganism from the genus Pseudomonas. 16 . The microorganism of claim 15 , wherein the microorganism is a strain of P. putida, P. fluorescens , or P. stutzeri. 17 . The microorganism of claim 16 , wherein the microorganism is a strain of P. putida KT2440. 18 . A process for producing muconic acid, the process comprising contacting a culture broth containing lignin depolymerization compounds with the microorganism of claim 1 . 19 . The process of claim 18 , wherein the lignin depolymerization compounds comprise at least one of p-coumaric acid, ferulic acid, benzoic acid, phenol, coniferyl alcohol, caffeic acid, vanillin, or 4-hydroxybenzoic acid, and at least a portion of the lignin depolymerization compounds are converted to catechol, and at least a portion of the catechol is converted to muconic acid. 20 . A process for producing adipic acid, the process comprising: separating muconic acid from a culture broth comprising muconic acid, impurities, and a microorganism; purifying the separated muconic acid; and hydrogenating at least a portion of the purified muconic acid to produce the adipic acid. 21 . The process of claim 20 , wherein the separating comprises at least one of centrifugation or filtration to produce muconic acid that is substantially free of the microorganism. 22 . The process of claim 21 , wherein the purifying comprises contacting the separated muconic acid with an adsorbent, wherein the adsorbent removes at least a first portion of the impurities from the separated muconic acid. 23 . The process of claim 22 , wherein the adsorbent comprises activated carbon. 24 . The process of claim 23 , wherein the impurities removed comprise at least one of benzoic acid, protocatechuic acid or 4-hydroxybenzoic acid. 25 . The process of claim 20 , wherein the purifying comprises crystallizing at least a portion of the muconic acid from the separated muconic acid to form a muconic acid precipitate and a liquid that contains at least a portion of the impurities. 26 . The process of claim 25 , wherein the purifying further comprises: dissolving the muconic acid precipitate in a solvent, resulting in a liquid phase comprising muconic acid and a solid phase comprising at least a portion of the impurities; and separating the liquid phase from the solid phase. 27 . The process of claim 26 , wherein the separating is by at least one of filtration or centrifugation. 28 . The process of claim 26 , wherein the hydrogenation comprises contacting the liquid phase comprising muconic acid and diatomic hydrogen with a metallic catalyst. 29 . The process of claim 28 , wherein the metallic catalyst comprises at least one of palladium, platinum, ruthenium, or rhodium. 30 . The process of claim 29 , wherein the at least one of palladium, platinum, ruthenium, or rhodium is supported by activated carbon or silica. 31 . The process of claim 30 , wherein the metallic catalyst comprises rhodium supported by activated carbon.
Catechol 1,2-dioxygenase (1.13.11.1) · CPC title
3-Dehydroshikimate dehydratase (4.2.1.118) · CPC title
Protocatechuate decarboxylase (4.1.1.63) · CPC title
Lyases (4.) · CPC title
Polycarboxylic acids · CPC title
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