CA2494664A1 - Production of a fermentation product - Google Patents

Production of a fermentation product Download PDF

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Publication number
CA2494664A1
CA2494664A1 CA002494664A CA2494664A CA2494664A1 CA 2494664 A1 CA2494664 A1 CA 2494664A1 CA 002494664 A CA002494664 A CA 002494664A CA 2494664 A CA2494664 A CA 2494664A CA 2494664 A1 CA2494664 A1 CA 2494664A1
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CA
Canada
Prior art keywords
acid
polysaccharide
process according
fermentation
enzyme
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CA002494664A
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French (fr)
Other versions
CA2494664C (en
Inventor
Jonathan Hughes
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ciba Specialty Chemicals Water Treatments Ltd
Original Assignee
Ciba Specialty Chemicals Water Treatments Limited
Jonathan Hughes
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
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Application filed by Ciba Specialty Chemicals Water Treatments Limited, Jonathan Hughes filed Critical Ciba Specialty Chemicals Water Treatments Limited
Publication of CA2494664A1 publication Critical patent/CA2494664A1/en
Application granted granted Critical
Publication of CA2494664C publication Critical patent/CA2494664C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/02Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/04Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • C12P7/06Ethanol, i.e. non-beverage
    • C12P7/08Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate
    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13KSACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
    • C13K1/00Glucose; Glucose-containing syrups
    • C13K1/02Glucose; Glucose-containing syrups obtained by saccharification of cellulosic materials
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or diesel

Abstract

A process of producing fermentation product comprising the steps of, (i) forming an acidified suspension of particulate plant derived material comprising a first polysaccharide which is more readily hydrolysable and a second polysaccharide which is more difficult to hydrolysable, (ii) allowing the first polysaccharide to undergo hydrolysis by action of the acid at a temperature of at least 50~C under conditions such that the first polysaccharide is hydrolysed and thereby forming a mixture of an aqueous liquor containing dissolved sugar and a solid residue containing the second polysaccharide, (iii) subjecting the mixture to one or more separation stage s in which the solid residue and aqueous sugar liquor are substantially separated from each other, (iv) optionally washing the residue substantially free of acid and sugar, (v) adjusting the pH of the aqueous liquor to at lea st 4, (vi) passing the aqueous liquor from step (iv) into a fermentation stage where the dissolved sugars are acted upon by a microorganism in a fermentati on broth to produce a fermentation product, (vii) contacting the second polysaccharide by an enzyme, said enzyme hydrolyses the second polysaccharid e to the component sugars, and allowing the component sugars to be acted upon by a microorganism in the fermentation brothto produce the fermentation product , (viii) separating the fermentation product from the broth, characterised in that the separation stage(s) in step (iii) is/are assisted by flocculation o f the solid by-product, employing one or more flocculating agent(s) selected from the group consisting of water soluble polymers, water swellable polymer s and charged microparticulate material. Typically such fermentation products include for instance ethanol, glycerol, acetone, n-butanol, butanediol, isopropanol, butyric acid, methane, citric Acid, fumaric acid, lactic acid, propionic acid, succinic acid, itaconic acid, acetic acid, acetaldehyde, 3- hydroxypropionic acid, glyconic acid, tartaric acid and amino acids such as L- glutaric acid, L-lysine, L-aspartic acid, L-tryptophan, L-arylglycines or salts of any of these acids.

Claims (22)

1. A process of producing fermentation product comprising the steps of, (i) forming an acidified suspension of particulate plant derived material comprising a first polysaccharide which is more readily hydrolysable and a second polysaccharide which is more difficult to hydrolyse, (ii) allowing the first polysaccharide to undergo hydrolysis by action of the acid at a temperature of at least 50°C under conditions such that the first polysaccharide is hydrolysed and thereby forming a mixture of an aqueous liquor containing dissolved sugar and a solid residue containing the second polysaccharide, (iii) subjecting the mixture to one or more separation stages in which the solid residue and aqueous sugar liquor are substantially separated from each other, (iv) optionally washing the residue substantially free of acid and sugar, (v) adjusting the pH of the aqueous liquor to at least 4, (vi) passing the aqueous liquor from step (iv) into a fermentation stage where the dissolved sugars are acted upon by a microorganism in a fermentation broth to produce a fermentation product, (vii) contacting the second polysaccharide by an enzyme, said enzyme hydrolyses the second polysaccharide to the component sugars, and allowing the component sugars to be acted upon by a microorganism in the fermentation broth to produce the fermentation product, (viii) separating the fermentation product from the broth, characterised in that the separation stages) in step (iii) is/are assisted by flocculation of the solid by-product, employing one or more flocculating agents) selected from the group consisting of water-soluble polymers, water-swellable polymers and charged microparticulate material.
2. A process according to claim 1 in which the solid residue of step (iv) comprising the second polysaccharide is divided into a main stream and a secondary stream, and passing the main stream directly into the fermentation stage, wherein the secondary stream of polysaccharide residue is passed into an enzyme production stage, in which enzyme is generated by allowing fungi to act on the polysaccharide residue, resulting in the formation of enzyme and sugars resulting from the second polysaccharide contained within the secondary stream, then passing the enzyme and sugars of step (vi) into the fermentation stage, wherein the enzyme acts on the second polysaccharide in the fermentation vessel and hydrolyses the second polysaccharide to the component sugars.
3. A process according to claim 1 in which the solid residue of step (iv) comprising the second polysaccharide is passed to an enzyme treatment stage in which enzyme is generated by allowing fungi to grow on the polysaccharideand said enzyme hydrolyses the polysaccharide into the component sugars and then passing the resulting sugars into the fermentation stage in which the sugars are converted into the fermentation product.
4. A process according to any of claims 1 to 3 in which the plant derived material comprises materials selected from the group consisting of herbaceous biomass, softwood biomass, hardwood biomass, sewage sludge, paper mill sludge and the biomass fraction of municipal solid waste.
5. A process according to any of claims 1 to 4 in which the plant derived material is cellulosic and comprises hemicellulose as the first polysaccharide and cellulose as the second polysaccharide.
6. A process according to any of claims 1 to 5 in which the acid has a pKa of below 4 and has a concentration up to 2% by weight.
7. A process according any of claims 1 to 6 in which the acid is selected from sulphuric acid and hydrochloric acid.
8. A process according to any of claims 1 to 7 in which the hydrolysis of the first polysaccharide is conducted at a temperature of between 120 to 220°C for a period of from 1 minute to 15 minutes.
9. A process according to any of claims 1 to 8 in which the flocculating agent is selected from the group consisting of water soluble or water swellable natural, semi-natural and synthetic polymers.
10. A process according to claim 9 in which the polymer is formed from a water soluble monomer or blend of monomers.
11. A process according to claim 9 in which the polymer is selected from the group consisting of polyacrylate salts, polyacrylamide, copolymers of acrylamide with (meth) acrylic acid or salts thereof, copolymers of acrylamide with dialkylaminoalkyl (meth) acrylate or acid addition or quaternary ammonium salts, polymers of diallyldimethyl ammonium chloride, polyamines and polyethylene imines.
12. A process according to any of claims 1 to 11 in which the flocculating agent is a charged microparticulate material.
13. A process according to claim 12 in which the charged microparticulate material is selected from the group consisting of swellable clays, anionic, cationic or amphoteric microparticulate silica based materials and organic cross-linked polymeric microparticles.
14. A process according to any one of claims 1 to 13 in which flocculation is effected by employing a water soluble or water-swellable polymer and a charged microparticulate material.
15. A process according to any one of claims 1 to 14 in which flocculation is effected by introducing an anionic microparticle material into the mixture and then reflocculating by adding a substantially non-ionic polymer.
16. A process according to any one of claims 1 to 15 in which flocculation is effected by introducing a cationic polymer into the mixture and then reflocculating by adding an anionic microparticulate material.
17. A process according to any one of claims 1 to 16 in which flocculation is effected by introducing a cationic polymer into the mixture and then reflocculating by adding an anionic polymer.
18. A process according to any one of claims 1 to 17 in which flocculation is effected by introducing an anionic polymer into the mixture and then reflocculating by adding a cationic polymer.
19. A process according to any one of claims 1 to 18 in which the solid-by product material comprises lignin and analogous materials.
20. A process according to any of claims 1 to 19 in which the fermentation product is selected from the group consisting of ethanol, glycerol, acetone, n-butanol, butanediol, isopropanol, butyric acid, methane, citric acid, fumaric acid, lactic acid, propionic acid, succinic acid, itaconic acid, acetic acid, acetaldehyde, 3-hydroxypropionic acid, glyconic acid, tartaric acid and amino acids such as L-glutaric acid, L-lysine, L-aspartic acid, L-tryptophan , L-arylglycines or salts of any of these acids.
21. A process according to any of claims 1 to 20 in which the fermentation product is separated from the broth by passing the broth comprising the fermentation product into a distillation stage, where the fermentation compound is collected as a distillate and the residue 'still bottoms' is removed.
22. A process according to any one of claims 1 to 21 in which the fermentation product is separated from the broth by passing the broth comprising the fermentation product into a concentration stage, in which the fermentation compound is collected in the concentrate and extracted by at least one means selected from the group consisting of ion exchange, solvent extraction and electrodialysis.
CA2494664A 2002-08-05 2003-07-28 Production of a fermentation product Expired - Fee Related CA2494664C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0218019.8 2002-08-05
GBGB0218019.8A GB0218019D0 (en) 2002-08-05 2002-08-05 Production of a fermentation product
PCT/EP2003/008291 WO2004015145A1 (en) 2002-08-05 2003-07-28 Production of a fermentation product

Publications (2)

Publication Number Publication Date
CA2494664A1 true CA2494664A1 (en) 2004-02-19
CA2494664C CA2494664C (en) 2012-03-06

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Family Applications (1)

Application Number Title Priority Date Filing Date
CA2494664A Expired - Fee Related CA2494664C (en) 2002-08-05 2003-07-28 Production of a fermentation product

Country Status (14)

Country Link
US (1) US7455997B2 (en)
EP (1) EP1530646A1 (en)
CN (1) CN1325654C (en)
AU (1) AU2003250185B2 (en)
BR (1) BR0313272B1 (en)
CA (1) CA2494664C (en)
GB (1) GB0218019D0 (en)
IN (1) IN2005CH00131A (en)
MX (1) MX270158B (en)
NO (1) NO327342B1 (en)
PH (1) PH12005500085B1 (en)
PL (1) PL208652B1 (en)
WO (1) WO2004015145A1 (en)
ZA (1) ZA200500272B (en)

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Also Published As

Publication number Publication date
CN1325654C (en) 2007-07-11
NO327342B1 (en) 2009-06-15
AU2003250185A1 (en) 2004-02-25
IN2005CH00131A (en) 2007-03-30
PL208652B1 (en) 2011-05-31
ZA200500272B (en) 2006-07-26
EP1530646A1 (en) 2005-05-18
MXPA05001411A (en) 2005-04-11
AU2003250185B2 (en) 2008-05-08
GB0218019D0 (en) 2002-09-11
BR0313272B1 (en) 2014-04-15
CA2494664C (en) 2012-03-06
US7455997B2 (en) 2008-11-25
NO20050970L (en) 2005-02-23
MX270158B (en) 2009-09-18
US20050233031A1 (en) 2005-10-20
WO2004015145A1 (en) 2004-02-19
CN1675379A (en) 2005-09-28
PH12005500085B1 (en) 2010-06-15
BR0313272A (en) 2005-07-05
PL373121A1 (en) 2005-08-08

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