EP2250236A2 - Procédé de purification de biodiesel ou de précurseurs de biodiesel - Google Patents
Procédé de purification de biodiesel ou de précurseurs de biodieselInfo
- Publication number
- EP2250236A2 EP2250236A2 EP09714094A EP09714094A EP2250236A2 EP 2250236 A2 EP2250236 A2 EP 2250236A2 EP 09714094 A EP09714094 A EP 09714094A EP 09714094 A EP09714094 A EP 09714094A EP 2250236 A2 EP2250236 A2 EP 2250236A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- biodiesel
- glycoside
- enzyme
- mixture
- precursor
- 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.)
- Withdrawn
Links
- 239000003225 biodiesel Substances 0.000 title claims abstract description 160
- 238000000034 method Methods 0.000 title claims abstract description 76
- 239000002243 precursor Substances 0.000 title claims abstract description 53
- 229930182470 glycoside Natural products 0.000 claims abstract description 104
- 150000002338 glycosides Chemical class 0.000 claims abstract description 100
- 239000000203 mixture Substances 0.000 claims abstract description 94
- 102000004190 Enzymes Human genes 0.000 claims abstract description 72
- 108090000790 Enzymes Proteins 0.000 claims abstract description 72
- 239000003925 fat Substances 0.000 claims description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 41
- 239000012071 phase Substances 0.000 claims description 27
- 230000008569 process Effects 0.000 claims description 24
- 238000003776 cleavage reaction Methods 0.000 claims description 23
- 230000007017 scission Effects 0.000 claims description 23
- -1 Nanngmas Proteins 0.000 claims description 21
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- 235000019198 oils Nutrition 0.000 claims description 18
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- 239000012084 conversion product Substances 0.000 claims description 13
- 238000000926 separation method Methods 0.000 claims description 12
- 235000013311 vegetables Nutrition 0.000 claims description 12
- 241001465754 Metazoa Species 0.000 claims description 11
- 238000011534 incubation Methods 0.000 claims description 9
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- BTEISVKTSQLKST-UHFFFAOYSA-N Haliclonasterol Natural products CC(C=CC(C)C(C)(C)C)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC12C BTEISVKTSQLKST-UHFFFAOYSA-N 0.000 claims description 2
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- OILXMJHPFNGGTO-UHFFFAOYSA-N (22E)-(24xi)-24-methylcholesta-5,22-dien-3beta-ol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(C)C(C)C)C1(C)CC2 OILXMJHPFNGGTO-UHFFFAOYSA-N 0.000 claims 1
- OQMZNAMGEHIHNN-UHFFFAOYSA-N 7-Dehydrostigmasterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CC(CC)C(C)C)CCC33)C)C3=CC=C21 OQMZNAMGEHIHNN-UHFFFAOYSA-N 0.000 claims 1
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- LGJMUZUPVCAVPU-UHFFFAOYSA-N beta-Sitostanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 LGJMUZUPVCAVPU-UHFFFAOYSA-N 0.000 claims 1
- HCXVJBMSMIARIN-PHZDYDNGSA-N stigmasterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)/C=C/[C@@H](CC)C(C)C)[C@@]1(C)CC2 HCXVJBMSMIARIN-PHZDYDNGSA-N 0.000 claims 1
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- 235000016831 stigmasterol Nutrition 0.000 claims 1
- BFDNMXAIBMJLBB-UHFFFAOYSA-N stigmasterol Natural products CCC(C=CC(C)C1CCCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C BFDNMXAIBMJLBB-UHFFFAOYSA-N 0.000 claims 1
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- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
- 239000008103 glucose Substances 0.000 description 9
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- 150000001875 compounds Chemical class 0.000 description 8
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- 230000002255 enzymatic effect Effects 0.000 description 8
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- 235000003702 sterols Nutrition 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 7
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- 238000006136 alcoholysis reaction Methods 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
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- 239000003054 catalyst Substances 0.000 description 5
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- 108010047754 beta-Glucosidase Proteins 0.000 description 4
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- 239000007979 citrate buffer Substances 0.000 description 4
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- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 4
- 229940093633 tricaprin Drugs 0.000 description 4
- LWFUFLREGJMOIZ-UHFFFAOYSA-N 3,5-dinitrosalicylic acid Chemical compound OC(=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O LWFUFLREGJMOIZ-UHFFFAOYSA-N 0.000 description 3
- 101710130006 Beta-glucanase Proteins 0.000 description 3
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- 239000002253 acid Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 3
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- 229940106157 cellulase Drugs 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 3
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- MSPCIZMDDUQPGJ-UHFFFAOYSA-N N-methyl-N-(trimethylsilyl)trifluoroacetamide Chemical compound C[Si](C)(C)N(C)C(=O)C(F)(F)F MSPCIZMDDUQPGJ-UHFFFAOYSA-N 0.000 description 2
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J17/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, having an oxygen-containing hetero ring not condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J17/005—Glycosides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
- C10G3/42—Catalytic treatment
- C10G3/44—Catalytic treatment characterised by the catalyst used
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/649—Biodiesel, i.e. fatty acid alkyl esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1003—Waste materials
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1011—Biomass
- C10G2300/1014—Biomass of vegetal origin
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1011—Biomass
- C10G2300/1018—Biomass of animal origin
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
Definitions
- the invention relates to a process for the purification of biodiesel, biodiesel precursors, vegetable or animal fats, and mixtures thereof, as well as the purified products obtainable by this process.
- the present invention describes the use of at least one enzyme that can cleave or convert glycoside, for the purification of biodiesel, biodiesel precursors, vegetable or animal fats, and mixtures thereof.
- Biodiesel is produced by alcoholysis of triglycerides, one mole of triglyceride reacting with three moles of alcohol to one mole of glycerol and three moles of the corresponding fatty acid ester. The reaction involves three reversible reactions in which the triglyceride is gradually transformed into a diglyceride, a monoglyceride, and finally glycerol.
- the transesterification can be carried out as a one-step process. However, it is also possible to carry out the transesterification in several stages. Only one part of the required methanol is added in each step and the glycerine phase is separated off after each step. In addition, the alcoholysis can be carried out under both acidic and basic catalysis.
- the alcoholysis of the triglycerides is carried out under homogeneous alkaline catalysis.
- the alkoxide ion acting as a catalyst is produced by dissolving, for example, an alkali metal alcoholate in the alcohol or reacting the pure alkali metal with the alcohol.
- methanolysis a corresponding alkali metal hydroxide can also be dissolved in the methanol. Since alcoholysis of triglycerides leads to relatively rapid phase separation by the glycerol formed, the predominant portion of the alkaline catalyst is removed relatively rapidly from the reaction mixture. The resulting fatty acid esters are therefore hardly in contact with the catalyst, so that the risk of saponification is low.
- the catalyst is usually in an amount of 0.5 to 1 part by weight used.
- the triglycerides used as starting materials for biodiesel production can be obtained, for example, from vegetable or animal fat.
- vegetable raw materials four main raw materials are used in the world-wide production of biodiesel, with rapeseed oil being the most important source, followed by sunflower oil, soybean oil and palmol.
- Other starting materials of commercial importance are animal fats, such as beef tallow, and used cement fats.
- the fuels based on renewable raw materials should have no or only minimal amounts of interfering ingredients.
- a process should help to separate compounds that can lead to precipitation of solids so that potential formation of deposits can be avoided.
- such a process should be substantially inexpensive and avoid expensive process steps, such as low temperature filtration.
- biodiesel or Biodiesel precursors and mixtures thereof containing at least one glycoside, wherein biodiesel or biodiesel precursor or a mixture is mkubiert thereof with at least one enzyme to convert a glycoside least the Minim ⁇ or cleave.
- the present invention teaches the use of at least one enzyme capable of cleaving or converting glycoside for purifying biodiesel or biodiesel precursors and mixtures thereof.
- the present invention provides biodiesel or biodiesel precursors and mixtures thereof which are obtainable by the process according to the invention.
- glycosides and, among these, especially the so-called steryl glycosides, for example the sitosteryl- ⁇ -glucoside, but also, for example, Cholesteryl glycosides can lead to turbidity and deposition the inventors have developed in numerous and extensive experiments, a reliable method that provides a substantial separation or conversion of glycosides in biodiesel or Biodiesel precursors and mixtures thereof. This method does not require extensive filtration after cooling, and can advantageously be carried out in some embodiments with only one process step.
- biodiesel and its meaning, and that during biodiesel production initially crude biodiesel can be obtained with lower purity, is known in the art.
- the term “biodiesel” may in particular also designate any mixture of fatty acid alkyl esters.
- the alkyl radical of the fatty acid alkyl ester may, for example, be straight-chain or branched and comprise 1 to 28 carbon atoms.
- the fatty acid alkyl ester may be, for example, a methyl, ethyl, propyl, butyl, pentyl, hexyl ester of a fatty acid.
- the mixture of fatty acid alkyl esters comprises one Content of at least 70 wt .-%, preferably of at least 85 Gew.-I, preferably of at least 95 Gew.-I, in particular of at least 98 Gew.-I of fatty acid alkyl esters, in each case based on the total weight of the organic constituents of the mixture.
- Biodiesel mixtures may contain any amount of mono-, di-, and / or tri-glycerides.
- biodiesel may have a limited content of mono-, di-, and / or tri-glycerides.
- the biodiesel may have a maximum content of 2% by weight, preferably 0.8% by weight for monoglycerides, a maximum level of 2% by weight, preferably 0.2% by weight for diglycerides, and / or have a maximum content of 2% by weight, preferably 0.2% by weight, of triglycerides, determined in accordance with the DIN standard DIN EN 14214.
- biodiesel precursor refers to any mixtures comprising mono-glycerides and / or di-glycerides and / or tri-glycerides of fatty acids.
- such mixtures may have a content of at least 30% by weight, preferably of at least 60% by weight, preferably of at least 85% by weight, in particular of at least 90% by weight, of mono-, di- or tri-glycerides , in each case based on the total weight of the organic constituents of the mixture.
- mixtures termed “biodiesel precursors” may optionally include fatty acid alkyl esters or fats.
- fat in the context of the present invention may refer to any mixture comprising triacylglycerides. As fat, both solid consistency, semi-solid consistency or liquid consistency at room temperature. In common usage, fats that are liquid at room temperature are often referred to as oils. It is to be expressly understood that the term “fats” in the context of the present invention also includes any oils, such as, for example, the fats which are referred to below as soybean oils, rapeseed oils, etc. according to the general language traditions. The selection of a fat or a mixture of fats may be made in accordance with the general knowledge of one skilled in the art.
- the fat is a fat or oil having a lecithin content of less than 10% by weight, in particular less than 5% by weight, more preferably less than 10 ppm, in particular less than 5 ppm.
- degummed and / or deodorized fats or oils are also preferred as well as biodiesel or biodiesel precursors having the above lecithin contents (phosphatidylcholine content).
- biodiesel or biodiesel precursors having the above lecithin contents phosphatidylcholine content
- glycosides refers generally to compounds consisting of carbohydrates (mono- or oligosaccharides) and aglycones (ie non-sugars). According to a preferred pect, the term compounds of a cyclic reaction Halbacetalformen of aldo or ketohexoses with Al ⁇ koholen to form an acetal (result "Lehrbuch der Organischen Chemie", Stuttgart, 1988, 21 ed., p 442 ff., ISBN 3-7776-0438-0 by H. Beyer, W. Walter).
- glycosides Depending on the particular underlying sugar is called the glycosides, as is known in the art, for example, as glucosides, mannosides, fructosides and depending on the presence of a heterocyclic 5 or 6 ring as furanosides or pyranosides de.
- glycosides also includes the oligo- or polysaccharides in which the glycosidic OH group is acetalated with egg ⁇ ner glycosidic or alcoholic group of an additional monosaccharide.
- Steryl glycosides are glycosides which are sterol-based as known to those skilled in the art.
- Sterols (often also referred to as sterols) as such are nitrogen-free, polycyclic, hydroaromatic compounds, in particular derivatives of gonan or of perhydro-1H-cyclopenta [alpha] phenanthrene.
- An overview of sterols, of which the corresponding steryl glycosides can be derived according to the knowledge of the skilled worker, can be found, for example, in: “Lexikon der Deutschen und der Deutschenchemie", Stuttgart, 2005, ISBN 3-8047-2275-X by W. Ternes et al. , P.
- US Pat. No. 7,091,012 describes methods for obtaining sterols and polar lipids from vegetable oil lecithin fractions.
- sterylglycosides u.a. Sitosteryl, Stigmasterol- or Campesterolbeta glucoside be called.
- the steryl glycosides in the educt material are used for the production of biodiesel (for example, vegetable or vegetable fats) are present in a form acylated in the 6-position of glucose (ie in a position at the Ce position of the glucose, in particular glucopyranose, at the original OH function) and in a transesterification to produce the biodiesel Cleavage of the ester bond takes place to form a steryl glycoside having a free OH group in the 6-position of the glucose.
- biodiesel for example, vegetable or vegetable fats
- the present invention now provides methods in which, under enzymatic action, glycosides, in particular steryl glycosides, are converted by enzyme incubation into a conversion product of the glycoside and / or into at least one cleavage product of the glycoside.
- glycosides in particular steryl glycosides
- the present invention employs chemical or biological conversion of potentially precipitating compounds. This allows a specific reduction of undesired glycosides.
- the conversion products there can be considered any compounds in which the glycosidic linkage between the sugar moiety and the non-sugar moiety of the glycoside remains intact, while as cleavage products, all compounds in which the glycosidic linkage between the sugar moiety and the non-sugar moiety is not intact can be considered remains and / or at least one, preferably at least two or three carbon atoms (e) comprehensive portion is cleaved from the glycoside.
- a suitable enzyme can be made taking into account the respective starting materials or starting material mixtures available on the basis of expert knowledge. In particular, the purity of the starting materials used and their origin (freshly obtained fats and oils or waste fats and oils) must be taken into account. In general, all enzymes having activity to convert or cleave glycosides are contemplated.
- the activity of a glycoside for example a glucoside, a cleaving or converting activity, may be a major or even a side activity of the enzyme (for example cellulases).
- enzymes can be used which have an activity for cleaving an acetal bond and / or for cleaving a glycosidic bond between the sugar moiety and the non-sugar moiety.
- hydrolases in particular glycosidases (EC 3.2.1 according to recommendations of the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology (NC-IUBMB)), such as, for example, alpha-amylase, beta-amylase, Exo-1, 4-alpha-D-glucosidase (glucoamylase), cellulase, polygalacturonase, lysozyme, alpha-D-glucosidase (maltase), beta-D-glucosidase, cellobiase, beta-glucanase, chitmase, anthocyanase, nanngmase, alpha-D-galactosidase, beta-D-galactosidase (lact
- glucosidases EC 3.2.1
- Glucosidases nanngmas
- ⁇ -glucanases ⁇ -glucanases
- cellulases glucosidases
- enzymes which have the activity of linking an aliphatic radical, in particular a long-chain radical, to the glycoside.
- an aliphatic radical in particular a long-chain radical
- the addition to the O atom of an alcohol group -CH (OH) - to form a group -CH (OR) - take place.
- the R radical to be linked may be, for example, a straight-chain or branched alkyl, (-C (O) -alkyl) -, (-C (O) -alkenyl) or alkenyl radical, which is preferably at least 6, preferably at least 14, in particular at least 16 carbon atoms, and which in the case of a (-C (0) -alkenyl) - or alkenyl may have one, two, three or more double bonds.
- the attachment to the OH group can take place at the C ⁇ position of the sugar, for example of the glucose component.
- esterases and / or acylases and / or transesterases and / or transferases can be used as enzyme, in particular if they have the above-described activity for attaching an alkyl, (-C (O) -alkyl) - , - (C (O) alkenyl) or alkenyl radicals.
- Examples include the swamp liver esterase (PLE, EC 3.1.1.3), penicillin acylase (EC 3.5.1.11) or various ammosaureacylases (EC 3.5.1.14).
- Conversion of a glycoside to an alkyl, (-C (O) -alkyl), (-C (O) -alkenyl) or alkenyl radical may occur.
- glycosides in particular sterol glycosides or glucosides, in which a fatty acid residue on the OH group was present at the C ⁇ position of the sugar used in the conversion of the fats, in particular by transesterification, for example with methanol, to give a less soluble non-acylated steryl glycoside was lost.
- esterases and / or acylases and / or transesterases and / or transferases it is particularly advantageous that fatty acids are already present in not insignificant amounts as impurities in biodiesel, biodiesel precursors or fats.
- a substrate for the enzyme is already present in situ, which can link to the OH group at the C ⁇ position of the sugar component of the glycoside, in particular the glucose Baustems of a glucoside.
- a glycoside conversion product or the at least one cleavage product of the glycoside can have higher solubility in the biodiesel, the biodegradable precursor, the vegetable or animal fats, and mixtures thereof than the glycoside itself. This is especially true This is the case when the glycoside has a hydrophobic section or a section comprising hydrophobic subregions which, after enzymatic cleavage, has higher solubility in the biodiesel, vegetable or animal fats and mixtures thereof than the glycoside present prior to the enzymatic incubation.
- the cleavage products obtained after cleavage from a steryl glycoside and containing the steryl radical or portions of the steryl radical have a higher solubility in biodiesel or precursors.
- a product obtained by the enzyme incubation ⁇ conversion product of the glycoside or the at least one cleavage product of the glycoside may have a lower solubility in the biodiesel, vegetable or animal fats or mixtures thereof comprise as the glycoside itself and are subsequently separated.
- the glycoside comprises a hydrophilic or less lipophilic section or a section with hydrophilic or comparatively less lipophilic subregions, which after enzymatic cleavage has a lower solubility in the biodiesel or the biodiesel precursor as well as its Mixtures than the present before the enzymatic incubation glycoside.
- this may be the case when the enzyme cleaves off a compound having at least one sugar moiety or moiety, in particular an aldo or ketohexose moiety, from a glycoside, in particular a stery glycoside.
- the separation of the conversion product of the glycoside or the at least one cleavage product of the glycoside may then particularly, but not exclusively, carried out in each case advantageous, for example by sedimentation or Filt ⁇ ration, without prior cooling.
- a separation of the glycoside conversion product and / or the at least one cleavage product of the glycoside can take place by conversion into a solvent phase in which this or these have a higher solubility than in the biodiesel or the biodiesel precursor, or the mixture thereof.
- a solvent phase it is possible for a person skilled in the art, on the basis of his knowledge, to choose any solvent which, after thorough mixing with biodiesel or biodiesel precursor or mixtures thereof, separates again from these at least after several hours and a phase above or below the phase which comprises the major part of the biodiesel to be purified or the biodiesel precursor or mixtures thereof.
- the solvent phase prior to use in the process according to the invention is an aqueous phase which consists of water or is more than 50% by weight, preferably more than 85% by weight more than 95 wt .-%, based on the total weight of the solvent phase comprises water.
- Aqueous solvent phases prior to use in the process according to the invention are also referred to below as aqueous dispersion mixtures.
- Further ingredients may be any additives selected on the basis of professional knowledge, for example one or more organic solvents, salts of organic or inorganic acids or bases, organic and inorganic acids, bases, pH-buffering mixtures, phase transfer auxiliaries, detergents, and one or more enzymes.
- the solvent phase before use in the process according to the invention is preferably water or an aqueous cleaning mixture, as explained below.
- the solvent phase prior to use in the method according to the invention is a solution or suspension which comprises water and at least one water-soluble enzyme.
- the amount of the at least one enzyme based on the amount of water may be, for example, in a range of 0.01 - 20 g per liter.
- erfmdungsgeschreibe method comprises the following steps:
- no filtration in particular no ultrafiltration, is carried out.
- the present invention provides an embodiment of the erfmdungsgedorfen method that is extremely advantageous and it manages to take advantage of the cleaning over a two-phase system.
- the step of incubating with the at least one enzyme comprises several steps, wherein in a first step, contacting a starting mixture, the biodiesel or biodiesel precursor or a mixture thereof, and in addition or more glycosides, with water or an aqueous cleaning mixture.
- contacting occurs for a sufficient amount of time to at least partially convert or cleave the one or more glycosides through the at least one enzyme.
- the duration of this period can be determined by a person skilled in the art on the basis of his general knowledge by simple experiments, for example by reducing the sugar content of the aqueous phase. follows wxrd as explained below.
- the reaction temperature may be between 15 0 C and 80 0 C, preferably 30 0 C and 60 0 C, the reaction time between 1 min and 24 hours, preferably 20 and 240 mm.
- the mixing can take place by means of a rotary or pumping over.
- a separation of a phase that is to say of an aqueous mixture, from the purified starting mixture takes place.
- the separated aqueous phase is now at least one conversion product of the glycoside or at least one cleavage product of the glycoside.
- the at least one enzyme is partially or completely soluble in water.
- this or this enzyme (s) will remain completely or substantially completely in an aqueous phase after it has been contacted with a phase comprising biodiesel or biodiesel precursor or mixtures thereof.
- Substantially complete retention in an aqueous phase means that more than 90%, preferably more than 96%, preferably more than 99% of the amount of the enzyme m remains in the aqueous phase.
- a two (multi) phase system makes it possible on the one hand to easily separate conversion or splitting products of the glycoside. In addition, this ensures that no or substantially no enzyme or parts of the enzyme preparation enters the mixture to be purified, and then in the final product, the fuel based on renewable raw materials, can potentially lead to problems.
- Particularly preferred is the use of a two-phase system, starting from a continuous Olphase or Ii pophilen phase with the biodiesel, the biodiesel precursor or the mixture thereof (and not a suspension, or the like, especially no lecithin successionn suspension) and a continuous aqueous phase with the at least one enzyme.
- glycosides comprising hydrophilic and hydrophobic moieties for example, steryl glycosides
- the biodiesel-water interface and / or biodiesel precursor-water interface
- hydrophobic glycosyl radical for example the steryl radical
- the method may additionally comprise a further washing step, for example a so-called water wash, before or after the step of incubation, or the incubation may be integrated into the water wash customarily occurring in the production of biodiesel.
- a further washing step for example a so-called water wash, before or after the step of incubation, or the incubation may be integrated into the water wash customarily occurring in the production of biodiesel.
- Biodiesel is subjected in its preparation according to a possible embodiment of a water wash.
- the water wash can be done in one or more stages.
- the raw biodiesel is mixed with water, the amount of water, based on the biodiesel, being selected in the range of preferably 2 to 10% by weight, preferably 4 to 8% by weight.
- the mixture is easily agitated, with the intensity of the movement chosen so that no stable emulsion is formed.
- the temperature of the water phase is preferably selected in the range of 20 to 90 0 C, particularly preferably 40 to 80 0 C.
- the duration of treatment of biodiesel with water depends on the quantities chosen. Preferably, the duration is chosen in the range of 5 to 45 minutes.
- the water washing step is preferably repeated at least once after separation of the water phase, wherein the amount of water and the water temperature can also be selected differently for the first water washing step.
- the oil is preferably dried.
- the biodiesel can be be erhxtzt, preferably to a temperature of more than 90 0 C.
- biodiesel precursor for example, soybean oil, palmol, corn oil, sunflower oil, waste edible fats and oils and / or beef tallow can be purified in particularly good successes with the process according to the invention.
- biodiesel has proved to be particularly advantageous to purify, which was made partially or completely from soybean oil, palmol, corn oil, sunflower oil and / or beef tallow.
- inventive method can be used with very good results for the purification of contaminated or waste products incurred as fats, for example Frittierolen.
- the crude biodiesel used in the process according to the invention is preferably obtained by alcoholysis of triglycerides.
- the triglycerides can be obtained per se from any suitable source of oils and fats.
- the alcoholysis is carried out according to known methods, acidic or, preferably, alkaline catalysts can be used.
- the alcohol used is preferably methanol. But it is also possible to use other alcohols, such as ethanol or propanol. Ethanol offers the possibility of extracting the biodiesel completely from biological sources, since ethanol can be obtained by fermenting organic matter.
- sterylglycoside precipitates particularly affects soybean oil and palmol, as well as biodiesel or biodiesel precursors from soybean oil and palmol owing to the high concentrations of sterylglycosides present therein.
- biodieses which are problematic from the point of view of the formation of precipitation
- the method according to the invention was able to achieve particularly good results, and the danger of a potential formation of be counteracted. Removal of steryl glycosides is also advantageous in particular because they can require or induce the precipitation of other substances.
- the glycoside to be at least partially cleaved or converted by the method according to the invention may in particular be a glucoside, mannoside, fructoside. Particularly good results were obtained with the erfmdungsgespecializeden process with a separation of Sterylglycosiden, preferably Sterylglucosiden, preferably s tosteryl, Stigmasterol- and Campesterol beta-glucosiden.
- the present invention also teaches the use of at least one enzyme which can cleave or convert glycoside for purifying biodiesel, biodiesel precursor, vegetable or animal fats, and mixtures thereof.
- Biodiesel or biodiesel precursors and mixtures thereof which are obtainable by the process according to the invention have a reduced content of glycosides, in particular of steryl glycosides, and thus have a reduced tendency to form clogs or deposits.
- the present invention therefore makes it possible to provide consumers with fuels based on renewable resources in improved Qualltat.
- the invention therefore relates to the use of at least one enzyme which can cleave or convert glycoside, for improving the storage stability and / or the filterability of biodiesel, or of a biodiesel precursor and mixtures thereof, in particular at temperatures below 40 ° C, preferably below 30 0 C, most preferably below 20 0 C.
- bio-filter cking tests have shown that the inventive treatment of biodiesel, a biodiesel precursor and mixtures thereof with at least one enzyme that can cleave or convert glycoside, can delay or prevent clogging of the filter Suitable filter block tests are described, for example, in WO
- Suitable filter block tests include the test described on page 5 below / page 6 above of WO 2007/076163 A2, the methods according to IP387 and ASTM D2068 and a modified ASTM 6217 test according to pages 13 to 15 of WO 2007/076163 A2.
- the enzymes used were ⁇ -glucosidases from various organisms, Narmgmase, cellulase, ⁇ -glucanase, lactase and various hemicellulases, all available from ASA Spezialenzymes GmbH, Wolfenbuttel, DE.
- the enzymatic cleavage of the sterylglycosides was measured by the following method: the respective enzyme tested was dissolved or dispersed in an aqueous buffer mixture. One part by volume of this aqueous buffer / enzyme mixture was mixed with 10 parts by volume of biodiesel in a beaker or test tube (depending on the volume size) and placed on the magnetic stirrer at the speaking reaction times and temperatures with stirring mcu- biert. After completion of the reaction, the aqueous phase was separated with a separatory funnel or by Zent ⁇ fugation and examined the Sterylglycosidgehalt of biodiesel by HPLC. Furthermore, the water content and the acid number were determined.
- the reducing sugars were measured by DNSS method.
- a) the biodiesel was treated only with buffer without enzyme
- DNSS method determination of glucose content (measurement of reducing sugars)
- test method follows instructions from ASA Spezialenzyme GmbH, D-38302 Wolfenbuttel, Germany.
- Glucose is detected photometrically with 3,5-dinitrosalicylic acid (DNSS).
- DNSS 3,5-dimtrosalicylic acid
- DNSS 3,5-dimtrosalicylic acid
- reducing sugars in alkaline medium
- 3-ammo-5-nitrosalicylic acid is formed.
- a nitro group is reduced to the amino group, while the aldehyde group of the monosaccharide to the carboxyl group oxidized (Kakac, B., Vejdelek, ZJ: Handbook of photometric analysis, Vol. I, Verlag Chemie, Weinheim 1974).
- Different sugars give different colorations, their absorption maximum between 500 and 550 nm.
- mono-, di-, oligo- and polysaccharides as well as methylpentoses and 0-methylsaccharides can also be detected with this test.
- DNSS Phenol Reagent Solution A: Weigh out 38.55 g K-Na tartrate into a 200 mL beaker and distil in 125 mL dist. Dissolve water, 2.425 g of NaOH (small plates) are dissolved in the solution.
- Solution B 1.325 g of 3,5-dinitrosalicylic acid (C 7 H 4 N 2 O 7 ; 2-hydroxy-3,5-di-nitrobenzoic acid) in a brown screw-cap bottle in 125 ml of dist. Water loose.
- Solution C 1.05 g of phenol in 12.5 mL of dist. Water loose. Add successively 0.25 g of NaOH (cookies) and 1.05 g of Na 2 SO 4 and dissolve while stirring.
- Working solution Solution A and solution C are poured into solution B (without rewinding) and homogenized for 10 min. Leave the solution for at least one night before use and always store in the dark.
- Blank values Mix 1.0 mL of water with 2.0 mL of DNSS phenol reagent and boil for 5 min. Cool the mixture for about 5 minutes in an ice bath and measure the extinction at room temperature and 546 nm.
- Standard Mix 1.0 mL dil. Standard solution (see table Calibration) with 2.0 mL DNSS phenol reagent and boil for 5 min. Cool the mixture for about 5 minutes in an ice bath and measure the extinction at room temperature and 546 nm.
- Calibration Dilutions of the standard solution for creating the calibration line:
- Carrier gas helium
- Target TIC 10000 counts Prescan Ionization Time: 100 ⁇ sec
- the sterylglucosides are identified and quantified with the external calibration in the samples.
- the enzymes ⁇ -glucosidase 1 (enzyme 1) and 2 (enzyme 2) were dissolved in 80 ml of 0.05 M Na citrate buffer, pH 5.0, and mixed with 800 ml of sterylglycoside biodiesel. D ⁇ ese mixture was placed in a 1 L beaker and incubated on the magnetic stirrer for 1 hr. At 37 0 C with stirring.
- the aqueous phase was separated with a separatory funnel and examined the Sterylglycosidgehalt of biodiesel by HPLC. Furthermore, the water content and the acid number were determined. In the aqueous subphase, the reducing sugars were measured by DNSS method.
- Table 1 shows a comparative overview of sterol glycoside content ("SG”, given in [ppm]; " ⁇ NG”: below the detection limit).
- the data show that the sterol glycoside content of the biodiesel sample is reduced below the detection limit by the different enzymatic treatments of 10 ppm.
- the enzyme ⁇ -glucosidase 1 is dissolved in different concentrations in 0.3 ml aqueous 0.05 M citrate buffer, pH 5.0, and treated with 3 ml of biodiesel as under methods, 2. measuring method.
- the results in Table 2 show that increasing amounts of reducing sugars are extracted into the aqueous lower phase with increasing enzyme dosage.
- the enzyme ⁇ -glucosidase 1 is dissolved at a concentration of 1.6 g / L in 0.3 ml aqueous 0.05 M citrate buffer, pH 5.0, and incubated with 3 ml biodiesel at different reaction times, otherwise as under Methods, 2. Measurement method, described, treated.
- Table 4 shows that in addition to beta-glucosidase numerous other enzymes can be used in the inventive method.
- beta-glucanase, naringinase, and cellulase are suitable.
- the inventive method can be used not only for the cleavage of steryl glycosides from biodiesel but also for the cleavage of steryl glycosides from vegetable oils. This procedure is analogous.
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Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09714094A EP2250236A2 (fr) | 2008-02-28 | 2009-03-02 | Procédé de purification de biodiesel ou de précurseurs de biodiesel |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08003709A EP2098585A1 (fr) | 2008-02-28 | 2008-02-28 | Procédé de nettoyage de biodiesel ou précurseurs du biodiesel |
PCT/EP2009/001468 WO2009106360A2 (fr) | 2008-02-28 | 2009-03-02 | Procédé de purification de biodiesel ou de précurseurs de biodiesel |
EP09714094A EP2250236A2 (fr) | 2008-02-28 | 2009-03-02 | Procédé de purification de biodiesel ou de précurseurs de biodiesel |
Publications (1)
Publication Number | Publication Date |
---|---|
EP2250236A2 true EP2250236A2 (fr) | 2010-11-17 |
Family
ID=39535234
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08003709A Withdrawn EP2098585A1 (fr) | 2008-02-28 | 2008-02-28 | Procédé de nettoyage de biodiesel ou précurseurs du biodiesel |
EP09714094A Withdrawn EP2250236A2 (fr) | 2008-02-28 | 2009-03-02 | Procédé de purification de biodiesel ou de précurseurs de biodiesel |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08003709A Withdrawn EP2098585A1 (fr) | 2008-02-28 | 2008-02-28 | Procédé de nettoyage de biodiesel ou précurseurs du biodiesel |
Country Status (3)
Country | Link |
---|---|
US (1) | US20110099889A1 (fr) |
EP (2) | EP2098585A1 (fr) |
WO (1) | WO2009106360A2 (fr) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0812559D0 (en) | 2008-07-09 | 2008-08-13 | Danisco | Method |
EP2406362A1 (fr) * | 2009-03-09 | 2012-01-18 | Novozymes A/S | Extraction enzymatique de glycosides stéryliques dans des esters alkyliques d'acides gras |
DE102010011606B4 (de) | 2010-03-16 | 2020-12-03 | Air Liquide Global E&C Solutions Germany Gmbh | Verfahren zur Aufarbeitung von Biodieselschlamm |
EP2447342A1 (fr) | 2010-10-26 | 2012-05-02 | Süd-Chemie AG | Procédé pour la production de biodiesel et d'un précurseur de biodiesel |
DE102010055159A1 (de) | 2010-12-18 | 2012-06-21 | Lurgi Gmbh | Verfahren zur enzymatischen Reinigung von Ölen pflanzlicher oder tierischer Herkunft |
AR091994A1 (es) * | 2012-03-16 | 2015-03-18 | Keclon S A | Metodo de remocion de esteril glicosidos |
US9957453B2 (en) | 2013-08-16 | 2018-05-01 | Eth Zurich | Enzymatic hydrolysis of acylated steryl glycosides and method for treating biofuel |
EP3404082A1 (fr) | 2017-05-19 | 2018-11-21 | GEA Mechanical Equipment GmbH | Procédé de réduction de la teneur en monoglycérides (mg), notamment en monoglycérides saturés (gmg) dans un biodiesel brut |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
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DE10333858A1 (de) * | 2003-07-24 | 2005-02-24 | Hans Jackeschky | Verfahren zur Aufbereitung von glycosidhaltigen Pflanzenölen und Verfahren zur Vorbehandlung von glycosidhaltigen Ölsaaten |
DE10353150A1 (de) * | 2003-11-14 | 2005-06-16 | Cognis Deutschland Gmbh & Co. Kg | Verfahren zur gleichzeitigen Herstellung von Sterolen und polaren Lipiden |
US20070151146A1 (en) * | 2005-12-29 | 2007-07-05 | Inmok Lee | Processes of Producing Biodiesel and Biodiesel Produced Therefrom |
-
2008
- 2008-02-28 EP EP08003709A patent/EP2098585A1/fr not_active Withdrawn
-
2009
- 2009-03-02 EP EP09714094A patent/EP2250236A2/fr not_active Withdrawn
- 2009-03-02 US US12/919,596 patent/US20110099889A1/en not_active Abandoned
- 2009-03-02 WO PCT/EP2009/001468 patent/WO2009106360A2/fr active Application Filing
Non-Patent Citations (1)
Title |
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See references of WO2009106360A2 * |
Also Published As
Publication number | Publication date |
---|---|
WO2009106360A3 (fr) | 2009-11-26 |
US20110099889A1 (en) | 2011-05-05 |
EP2098585A1 (fr) | 2009-09-09 |
WO2009106360A2 (fr) | 2009-09-03 |
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