WO2005058856A1 - A process for the liquefaction of lignocellulosic material - Google Patents
A process for the liquefaction of lignocellulosic material Download PDFInfo
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- WO2005058856A1 WO2005058856A1 PCT/EP2004/053450 EP2004053450W WO2005058856A1 WO 2005058856 A1 WO2005058856 A1 WO 2005058856A1 EP 2004053450 W EP2004053450 W EP 2004053450W WO 2005058856 A1 WO2005058856 A1 WO 2005058856A1
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- 0 *C(*)(C1(*)*)C(*)(*)OC1=O Chemical compound *C(*)(C1(*)*)C(*)(*)OC1=O 0.000 description 2
- GWKLJQUHAGESSH-UHFFFAOYSA-N CC(C(C1)C(C)(CC2)OC2=O)OC1=O Chemical compound CC(C(C1)C(C)(CC2)OC2=O)OC1=O GWKLJQUHAGESSH-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H8/00—Macromolecular compounds derived from lignocellulosic materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
Definitions
- the present invention relates to a process for the liquefaction of lignocellulosic or cellulosic material.
- Background of the invention It is known to produce levulinic acid by controlled acid hydrolysis of lignocellulosic material.
- Levulinic acid is a useful compound, since its reactive nature makes it a suitable intermediate for the production of commercially interesting compounds.
- levulinic acid is produced from cellulose or ligno-cellulose material by hydrolysing the material at a temperature between 210 and 230 °C in the presence of 1-5 % weight of mineral acid in a first reactor to obtain a hydroxymethylfurfural-containing intermediate product and further hydrolysing the intermediate product at a temperature between 195 and 215 °C in the presence of 3-7.5% weight of mineral acid in a second reactor.
- the temperature in the first and the second reaction vessel is controlled by injection of high pressure steam.
- the process pressure is above 200 psig (14 bar g) in the second vessel and much higher in the first vessel.
- liquefied lignocellulosic or cellulosic material as starting material for levulinic acid production processes or other chemical processes for the conversion of lignocellulose.
- a liquefied starting material for levulinic acid production or other biomass conversion processes might allow milder process conditions and allows the use of heterogeneous catalysis for further processing. It would further allow separation of contaminants from the desired components in the starting material.
- Reference herein to liquefied (ligno) cellulosic materials is to (ligno) cellulosic material dissolved in a liquid medium.
- Liquefaction of solid (ligno) cellulosic material is typically achieved by mildly heating the (ligno) cellulose with an organic solvent in the presence of an homogeneous acid catalyst. This treatment will result in some cleavage of covalent linkages of cellulose, hemicellulose and lignin and of covalent linkages between lignin and hemicellulose. Acids such as formic, acetic and propionic acid, ketones, aldehydes, sugars and lignin degradation products might be formed. It is known that biomass or lignocellulosic material can be liquefied at ambient pressure and moderate temperature in the presence of an acid catalyst by using solvents .
- EP 472 474 A for example, is described a process for liquefying lignocellulose substance by heating the substance at a temperature of 100 to 200 °C and ambient pressure in the presence of an acid catalyst and one or more polyhydric alcohols.
- Polyethylene glycol, polypropylene glycol, glycerin, ethylene glycol, 1,4-butanol, 1,6-hexanol and polycaprolactone are mentioned as possible polyhydric alcohols.
- Bioresource Technology 70 (1999) 61-67 the use of cyclic carbonates such as ethylene carbonate and propylene carbonate as solvents for the liquefaction of lignocellulosic material in the presence of an acid catalyst at 120-150°C has been described.
- Such compounds with a gamma lactone group are typically obtainable from levulinic acid, for example by hydrogenation and dehydration (in this case internal ester formation to form a lactone) or by aldolcondensation and dehydration, optionally in combination with hydrogenation.
- Compounds with a gamma lactone group that are not typically obtainable from levulinic acid, e.g. gamma butyrolactone also known as dihydrofuran-2 (3ff) -one, are also suitable as solvents for liquefaction of (ligno) cellulosic material at mild conditions.
- the present invention relates to a process for the liquefaction of lignocellulosic or cellulosic material, wherein solid lignocellulosic or cellulosic material is heated at a temperature in the range of from 100 to 300 °C in the presence of an acid catalyst and a solvent, wherein the solvent-to-solid material weight ratio is at most 50, the acid catalyst is present in a concentration of at most 50% by weight of acid based on the weight of solvent and acid, and the solvent comprises a compound having a gamma lactone group of the general molecular formula
- the invention further relates to the herein-above defined process for the liquefaction of lignocellulosic or cellulosic material, wherein the solvent comprises furfural, levulinic acid or a compound obtainable from furfural or levulinic acid by hydrogenation, dehydration, aldolcondensation, dimerisation or oligomerisation, esterification with an alcohol, or a combination of two or more of these reactions.
- the solvent can be obtained from the (ligno) cellulosic material by either a parallel or a (ligno) cellulose conversion process step.
- the solvent comprises a compound with a gamma lactone group.
- the solvent comprises furfural, levulinic acid, a compound obtainable from furfural, or a compound without a gamma lactone group obtainable from levulinic acid.
- the solvent may comprise two or more of these compounds.
- the solvent essentially consists of one or more of these compounds, i.e.
- references herein to a compounds having a gamma lactone group is to a compound according to general molecular formula (1), wherein R ⁇ to Rg are a H atom or an organic group as hereinabove defined.
- the total number of carbon atoms of the compound is preferably at most 20, more preferably at most 15.
- each of R]_ to R4 is a H atom. More preferably, each of R ⁇ to R4 is a H atom and R5 is a methyl group.
- Such compounds are gamma valerolactone (Rg is a H atom) , also known as 5-methyldihydrofuran-2 (3H) -one, 2-methyl-5- oxotetrahydrofuran-2-carboxylic acid (Rg is a carboxyl group) , a compound with a molecular structure according to any one of molecular formulas (2) to (5) , or an ester of a compound according to formula (2) or (3) :
- Gamma valerolactone can be obtained from levulinic acid by hydrogenation followed by dehydration (internal ester formation) .
- the compounds according to formulas (2) to (5) are levulinic acid dimers that may be obtained by contacting levulinic acid in the presence of hydrogen with a strongly acidic catalyst having a hydrogenating function, e.g. Pd/cation-exchange resin, at elevated temperature and preferably at elevated pressure. Typical process temperatures and pressures are in the range of from 60 to 170 °C and of from 1 to 200 bar (absolute) , respectively.
- a strongly acidic catalyst having a hydrogenating function e.g. Pd/cation-exchange resin
- the catalyst and process conditions of this process are similar to those applied in the known single-step process for the production of methyl isobutyl ketone from acetone.
- the solvent is a strong acid, such as for example 2-methyl-5- oxotetrahydrofuran-2-carboxylic acid, the use of additional acid may be redundant. It is therefore possible that the solvent and the acid are the same compound.
- Other compounds with a gamma lactone group suitable to be used as solvent in the liquefaction process according to the invention, which are obtainable by the above-mentioned levulinic acid dimerisation process, are the compounds with a molecular structure according to formula (6) or (7) or their esters:
- the ester preferably is an alkyl ester with an alcohol fragment with at most 10 carbon atoms, more preferably a linear alkyl ester with an alcohol fragment with at most 5 carbon atoms, even more preferably a methyl or an ethyl ester.
- Compounds with a gamma lactone group suitable to be used as solvent in the liquefaction process according to the invention may also be formed by dimerisation or oligomerisation of alpha angelica lactone.
- Alpha angelica lactone may be obtained from levulinic acid by internal ester formation (dehydration) of the enol form of the carbonyl group in levulinic acid.
- the compounds with a gamma lactone group are preferably obtainable from levulinic acid by hydrogenation, dehydration, aldolcondensation, dimerisation or oligomerisation, esterification with an alcohol, or a combination of two or more thereof. Examples of such compounds have been mentioned hereinabove.
- levulinic acid, furfural or compounds without a gamma lactone group that are obtainable from levulinic acid or furfural may be used as solvent in the process according to the invention.
- Examples of compounds suitable to be used as solvent in the process according to the invention that can be obtained from furfural are tetra hydrofurfuryl alcohol, furfuryl alcohol, diether of furfuryl alcohol, dimers or oligomers of furfural or furfuryl alcohol.
- Examples of suitable compounds without a gamma lactone group obtainable from levulinic acid are C5 compounds that can be obtained from levulinic acid by dehydration or dehydration in combination with hydrogenation, such as alpha-angelicalactone, 1, 4-pentanediol, 1-pentanol, 2-pentanol, or methyl tetrahydrofuran. The conversion of levulinic acid in these compounds is described in more detail in US 5,883,266.
- a suitable compound obtainable from levulinic acid is 4-methyl-6-oxononanedioic acid or a mono- or di-ester thereof.
- Such mono- or di-ester preferably has an alcohol fragment with at most 10 carbon atoms, more preferably a linear alcohol fragment with at most 5 carbon atoms, even more preferably is the di- methyl or the di-ethyl ester.4-methyl-6-oxononanedioic acid is the main dimer that is obtained in the above- described levulinic acid dimerisation process in the presence of hydrogen and a strongly acidic hydrogenation catalyst .
- esters of levulinic acid for example the ethylene glycol ester or alkyl esters of levulinic acid, more preferably alkyl esters with at most 10 carbon atoms in the alcohol fragment, even more preferably linear alkyl esters with at most 5 carbon atoms in the alcohol fragment, such as for example ethyl levulinate, butyl levulinate, or pentyl levulinate.
- the oligomer will typically contain at most ten monomer units, preferably at most five, since the solvent has to be a liquid under the process conditions.
- the solvent and the solid (ligno) cellulosic material are mixed in a solvent-to-solid weight ratio of at most 50.
- Reference herein to the weight of the solid material is to the dry solid material. Since the amount of solvent should be sufficient to wet the solid material, the solvent-to-solid weight ratio will typically be above 3.
- Acid is added in such amount that the acid concentration is at most 50% by weight based on the weight of solvent and acid.
- the acid may be an homogeneous or a finely dispersed colloidal acid, preferably a homogeneous acid.
- a strong mineral or organic acid is used. Reference herein to a strong acid is to an acid having a pKa value below 4.7.
- the acid has a pKa value below 3.5, even more preferably below 2.5.
- suitable strong mineral acids are sulphuric acid, para toluene sulphonic acid, phenol sulphonic acid, phosphoric acid, or hydrochloric acid.
- Preferred mineral acids are sulphuric acid or phosphoric acid, since they have a relatively high boiling point and thus remain liquid and stable at the process temperature at ambient pressure.
- Particularly preferred is phosphoric acid.
- phosphoric acid Compared to sulphur-containing acids, phosphoric acid has the advantage that recovered phosphoric acid can be converted into valuable products such as fertilizers and that it is less prone to coking.
- Suitable organic acids are strong organic acids that are liquid under the process conditions applied.
- Suitable organic acids are oxalic acid, formic acid, 2-oxo-propanoic acid (pyruvic acid) , lactic acid, citric acid, ( IE) -prop-l-ene-1, 2, 3-tricarboxylic acid, malonic acid, maleic acid, glycolic acid, 2-furoic acid, 5- (hydroxymethyl) -2-furoic acid, furan-2, 5-dicarboxylic acid, salicylic acid, 2, 4 , 5-trihydroxybenzoic acid, 2, 3-dihydroxysuccinic acid (tartaric acid), 2-methylenesuccinic acid (itaconic acid) .
- Preferred organic acids are oxalic acid, 2-oxo-propanoic acid, maleic acid, ( IE) -prop-l-ene-1, 2, 3-tricarboxylic acid, 2, 3-dihydroxysuccinic acid or furan-2, 5-dicarboxylic acid.
- a mixture of different acids may be used.
- the acid concentration is preferably at most 20% by weight, more preferably in the range of from 0.5 to 10% by weight, even more preferably of from 1 to 5% by weight.
- the solvent-to-solid weight ratio is preferably in the range of from 3 to 20, more preferably of from 5 to 15.
- the mixture of solids, solvent and acid is thus a non-aqueous mixture that may contain a small amount of water that is brought in with the acid.
- the solid (ligno) cellulose material will typically be finely divided, for example in the form of powder (e.g. sawdust), wood chips, cutted stalks, fibres or paper or the like. It will be appreciated that a smaller size of the material will result in a reduced liquefaction time. A larger size of the material may be combined with some mechanical action during the liquefaction process in order to achieve liquefaction within an acceptable time.
- the mixture of solids, solvent and acid is heated at a temperature in the range of from 100 to 300 °C, preferably of from 125 to 250 °C, more preferably of from 150 to 210 °C.
- the pressure is preferably in the range of from 0.1 to 15 bar (absolute), more preferably of from 0.5 to 10 bar (absolute), even more preferably of from 0.8 to 3 bar (absolute). Ambient pressure is most preferred.
- a considerable amount of the solid is liquefied, typically at least 50% (w/w) . It is possible to liquefy more than 80% (w/w) of the solid material at ambient pressure within a few hours.
- the solvent used in the liquefaction process according to the invention may be obtained from furfural or levulinic acid that is obtained from acid hydrolysis of (ligno) cellulosic material.
- the solvent may be obtained from the same (ligno) cellulosic material as used in the liquefaction process, either in a parallel process or in a process in series.
- a parallel process means that part of the (ligno) cellulosic material is subjected to an acid hydrolysis process to obtain levulinic acid, optionally in combination with furfural.
- the levulinic acid or furfural may then be used as such as solvent or may be further processed to obtain a solvent.
- the other part of the (ligno) cellulosic material is liquefied according to the process of the invention, using the solvent obtained from the same (ligno) cellulosic material.
- a process in series means that (ligno) cellulosic material is first liquefied according to the process of the invention and the liquefied (ligno) cellulosic material or the residue is then subjected to an acid hydrolysis process to obtain levulinic acid, optionally in combination with furfural. Part of the thus-obtained levulinic acid or furfural or a derivative thereof is then recycled to the liquefaction process as (make-up) solvent.
- the acid hydrolysis process to obtain levulinic acid may for example be a process as disclosed in US 5,608,105 or US 6,054,611.
- An advantage of the use of solvents that are derived from subsequent acid hydrolysis of the liquefied (ligno) cellulosic material is that the solvent does not need to be separated from the liquefied (ligno) cellulosic material, since the compound does not negatively influence the subsequent process step.
- Another advantage is that the acid catalyst does not need to be removed from the liquefied material, since the subsequent process is also a process using an acid catalyst.
- EXAMPLES 1-3 2 grams of dried birch (Betula ssp.) sawdust and 20 grams of gamma-valerolactone ( ⁇ VL) and an amount of phosphoric acid (85% by weight) were loaded in a 30 ml glass flask. The flask was placed in a silicon oil bath and heated. The amount of phosphoric acid, temperature, and duration of the experiment were varied. The flasks were cooled with water to end the experiment. The percentage of residue was determined by vacuum-filtering the content of the flask, followed by washing the residue with 150 ml of acetone/water (9:1 v/v) .
- EXAMPLE 4 2 grams of dried birch (Betula ssp.) sawdust, 10 grams of gamma-valerolactone, 10 grams of 1-pentanol and phosphoric acid were heated in an autoclave at a temperature of 230 °C during 16 minutes. The pressure reached 12.7 bar (absolute). The percentage of residue was determined as described above.
- EXAMPLE 5 2 gram of dried bagasse (20 mesh particles) , 20 grams of levulinic acid and sulfuric acid were loaded in a 30 ml glass flask. The flask was placed in a silicon oil bath and heated to 190 °C.
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Wood Science & Technology (AREA)
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
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Abstract
Description
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002549458A CA2549458A1 (en) | 2003-12-15 | 2004-12-14 | A process for the liquefaction of lignocellulosic material |
BRPI0417599-9A BRPI0417599A (en) | 2003-12-15 | 2004-12-14 | process for liquefaction of lignocellulosic or cellulosic material |
US10/582,888 US20070100162A1 (en) | 2003-12-15 | 2004-12-14 | Process for the liquefaction of lignocellulosic material |
AU2004298440A AU2004298440B2 (en) | 2003-12-15 | 2004-12-14 | A process for the liquefaction of lignocellulosic material |
EP04804809A EP1699771A1 (en) | 2003-12-15 | 2004-12-14 | A process for the liquefaction of lignocellulosic material |
JP2006544430A JP2007514047A (en) | 2003-12-15 | 2004-12-14 | Method for liquefaction of lignocellulose material |
Applications Claiming Priority (2)
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EP03257858 | 2003-12-15 | ||
EP03257858.5 | 2003-12-15 |
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WO2005058856A1 true WO2005058856A1 (en) | 2005-06-30 |
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PCT/EP2004/053450 WO2005058856A1 (en) | 2003-12-15 | 2004-12-14 | A process for the liquefaction of lignocellulosic material |
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US (1) | US20070100162A1 (en) |
EP (1) | EP1699771A1 (en) |
JP (1) | JP2007514047A (en) |
CN (1) | CN1894230A (en) |
AU (1) | AU2004298440B2 (en) |
BR (1) | BRPI0417599A (en) |
CA (1) | CA2549458A1 (en) |
RU (1) | RU2006125433A (en) |
WO (1) | WO2005058856A1 (en) |
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WO2007094922A2 (en) | 2006-01-20 | 2007-08-23 | Archer-Daniels-Midland Company | Levulinic acid ester derivatives as reactive plasticizers and coalescent solvents |
US7777085B2 (en) | 2008-10-01 | 2010-08-17 | Inventure Chemical, Inc. | Method for conversion of oil-containing algae to 1,3-propanediol |
US7943792B2 (en) | 2007-04-02 | 2011-05-17 | Inventure Chemical Inc. | Production of biodiesel, cellulosic sugars, and peptides from the simultaneous esterification and alcoholysis/hydrolysis of materials with oil-containing substituents including phospholipids and peptidic content |
US8003818B2 (en) | 2004-12-23 | 2011-08-23 | Shell Oil Company | Process for the hydrogenation of a lactone or of a carboxylic acid or an ester having a gamma-carbonyl group |
WO2011141545A1 (en) | 2010-05-12 | 2011-11-17 | Shell Internationale Research Maatschappij B.V. | Process for liquefying a cellulosic material |
WO2011141546A2 (en) | 2010-05-12 | 2011-11-17 | Shell Internationale Research Maatschappij B.V. | Process for liquefying a cellulosic material |
US8212062B2 (en) | 2007-04-02 | 2012-07-03 | Inventure Chemical, Inc. | Production of biodiesel, cellulosic sugars, and peptides from the simultaneous esterification and alcoholysis/hydrolysis of oil-containing materials with cellulosic and peptidic content |
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US8580978B2 (en) | 2009-08-07 | 2013-11-12 | Shell Oil Company | Process for preparing a hydroxyacid or hydroxyester |
US20150176090A1 (en) * | 2013-12-20 | 2015-06-25 | Wisconsin Alumni Research Foundation | Biomass pre-treatment for co-production of high-concentration c5- and c6-carbohydrates and their derivatives |
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2004
- 2004-12-14 BR BRPI0417599-9A patent/BRPI0417599A/en not_active IP Right Cessation
- 2004-12-14 WO PCT/EP2004/053450 patent/WO2005058856A1/en active Application Filing
- 2004-12-14 JP JP2006544430A patent/JP2007514047A/en active Pending
- 2004-12-14 EP EP04804809A patent/EP1699771A1/en not_active Withdrawn
- 2004-12-14 CN CNA200480037424XA patent/CN1894230A/en active Pending
- 2004-12-14 CA CA002549458A patent/CA2549458A1/en not_active Abandoned
- 2004-12-14 US US10/582,888 patent/US20070100162A1/en not_active Abandoned
- 2004-12-14 RU RU2006125433/04A patent/RU2006125433A/en not_active Application Discontinuation
- 2004-12-14 AU AU2004298440A patent/AU2004298440B2/en not_active Ceased
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Also Published As
Publication number | Publication date |
---|---|
AU2004298440A1 (en) | 2005-06-30 |
BRPI0417599A (en) | 2007-03-20 |
CN1894230A (en) | 2007-01-10 |
US20070100162A1 (en) | 2007-05-03 |
JP2007514047A (en) | 2007-05-31 |
CA2549458A1 (en) | 2005-06-30 |
RU2006125433A (en) | 2008-01-27 |
EP1699771A1 (en) | 2006-09-13 |
AU2004298440B2 (en) | 2007-10-04 |
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