AU2008286538A1 - Liquid biofuel made of esters and bound glycerides, and also process for production thereof - Google Patents
Liquid biofuel made of esters and bound glycerides, and also process for production thereof Download PDFInfo
- Publication number
- AU2008286538A1 AU2008286538A1 AU2008286538A AU2008286538A AU2008286538A1 AU 2008286538 A1 AU2008286538 A1 AU 2008286538A1 AU 2008286538 A AU2008286538 A AU 2008286538A AU 2008286538 A AU2008286538 A AU 2008286538A AU 2008286538 A1 AU2008286538 A1 AU 2008286538A1
- Authority
- AU
- Australia
- Prior art keywords
- biofuel
- triglycerides
- mass fraction
- fraction
- mass
- 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
Links
- 239000002551 biofuel Substances 0.000 title claims description 33
- 238000000034 method Methods 0.000 title claims description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 125000005456 glyceride group Chemical group 0.000 title description 5
- 150000002148 esters Chemical class 0.000 title description 4
- 239000007788 liquid Substances 0.000 title description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 35
- 150000003626 triacylglycerols Chemical class 0.000 claims description 33
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 23
- 229930195729 fatty acid Natural products 0.000 claims description 23
- 239000000194 fatty acid Substances 0.000 claims description 23
- 239000000446 fuel Substances 0.000 claims description 22
- 238000005809 transesterification reaction Methods 0.000 claims description 18
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 claims description 14
- 150000004665 fatty acids Chemical class 0.000 claims description 13
- 125000005907 alkyl ester group Chemical group 0.000 claims description 12
- 239000004367 Lipase Substances 0.000 claims description 11
- 102000004882 Lipase Human genes 0.000 claims description 11
- 108090001060 Lipase Proteins 0.000 claims description 11
- 235000019421 lipase Nutrition 0.000 claims description 11
- 102000004190 Enzymes Human genes 0.000 claims description 10
- 108090000790 Enzymes Proteins 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 10
- 239000008158 vegetable oil Substances 0.000 claims description 9
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 8
- 239000003225 biodiesel Substances 0.000 claims description 6
- 239000011541 reaction mixture Substances 0.000 claims description 5
- 238000002485 combustion reaction Methods 0.000 claims description 3
- 239000002803 fossil fuel Substances 0.000 claims description 2
- 235000019871 vegetable fat Nutrition 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 33
- 239000000203 mixture Substances 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000003925 fat Substances 0.000 description 5
- 235000019197 fats Nutrition 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 239000002283 diesel fuel Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
- 235000019484 Rapeseed oil Nutrition 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000001960 triggered effect Effects 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 235000019737 Animal fat Nutrition 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical group 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 235000014541 cooking fats Nutrition 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 239000002828 fuel tank Substances 0.000 description 1
- 238000007210 heterogeneous catalysis Methods 0.000 description 1
- 238000007172 homogeneous catalysis Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 235000019626 lipase activity Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 150000004666 short chain fatty acids Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
- C10L1/191—Esters ester radical containing compounds; ester ethers; carbonic acid esters of di- or polyhydroxyalcohols
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/026—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
- C11C3/003—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fatty acids with alcohols
-
- 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
- C12P7/6445—Glycerides
- C12P7/6458—Glycerides by transesterification, e.g. interesterification, ester interchange, alcoholysis or acidolysis
-
- 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
- C10G2300/1011—Biomass
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Emergency Medicine (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Fats And Perfumes (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Beans For Foods Or Fodder (AREA)
Description
WO 2009/021486 Al Liquid biofuel made from esters and bound glycerides, and also process for production thereof Technical field The present invention relates to a liquid biofuel having a basis of triglycerides, mono- and diglycerides, and alkylesters of fatty acids, and a process for production thereof. The fuel is particularly suitable as a substitute for conventional fuels, for example diesel. It is also possible to use it directly as a fuel in combustion engines. State of the art Biofuels and biofuel mixtures based on vegetable oil and animal fat are described for example in Patent Nos. DE 4116905 Cl, WO 95/25152 Al, EP 855436 A2, or US 5713965 A. These documents particularly disclose mixtures of rapeseed oils with petrol or diesel, to which an additional substance is added. In German Patent No. DE 4116905 C1, this additional component is an alcohol, in WO 95/25152 Al, it is an alkylester of a short-chain fatty acid having a maximum chain length of 6 C atoms, and in EP 855436 A2 it is an acetal. Patent specifications US 5713965 A, US 5480787 A and EP 1705238 Al (= WO 2005075615 Al) describe processes for the production of alkylesters of fatty acids by lipase catalysed transesterification of oils and fats. In these processes, the fatty acid alkylesters of bound and free glycerol are separated by known methods and accordingly are not used as a fuel fraction. Since the glycerol is separated, the yield relative to the feedstock oil or fat is only about 90%.
- 2 Patent specification EP 1126011 A2 describes a process for homoegenously catalysed transesterification of fats and oils under conditions in which at least one of the reactants is present in a critical state. As with the specifications cited in the preceding, US 5713965 A, US 5480787 A, and EP 1705238 Al, in this case too the glycerol produced is separated from the fatty acid alkylesters and is not used as a fuel fraction. Patent specification US 55788090 A describes a biofuel consisting of fatty acid alkylesters and bound glycerol. Unlike the fuel described in the present document, the bound glycerides are not present in the form of mono-, di-, and trialkylglycerol esters, but as mono-, di-, and trialkylglycerol ethers. These ethers are produced in a reaction that differs from transesterification, as intermediate products of the transesterification reaction. Patent specification US 5316927 A describes a process for producing monoglycerides and fatty acid alkylesters via lipase-catalysed transesterification of fats and oils. When the reaction is complete, the two products are separated from one another and fed to different applications. Diesel fuel is a refined petroleum product that represents a considerable portion of the international fuel market. Finite resources, dramatic price increases, and the ongoing debate regarding climate have led to renewed efforts to at least partially replace fossil diesel with fuels from renewable raw materials. At the moment, the most of such raw materials are drawn from vegetable oil and biodiesel (alkylesters of fatty acids). Vegetable oils largely consist of triglycerides, that is to say esters of glycerol, and three fatty acids, and in smaller quantities, free fatty acids.
-3 The use of pure vegetable oil as diesel fuel is not without certain difficulties. Because of its high viscosity and low cetane number, the triglycerides are only partially combusted, which results in deposits on valves and fuel injectors, and high emission values. Mixing vegetable oil with fossil diesel also presents problems, because such mixtures are unstable, particularly at low temperatures, and consequently there is a danger that they will separate in the fuel tank. These problems can be largely avoided by transesterification of triglycerides with a monovalent alcohol. The fatty acid alkylesters produced have a viscosity and cetane number similar to those of diesel, and are thus able to be used as a diesel substitute relatively easily. Besides alkylesters of fatty acids (biodiesel), transesterifying vegetable or animal oils or fats also produces about 10% free glycerol. Free glycerol is insoluble in biodiesel and therefore cannot be used as a fuel fraction. The separated free glycerol lowers the fuel yield of the process, and since it needs to undergo downstream processing and the revenue situation therefrom is unfavourable, it represents a not insignificant cost factor. A fuel that is produced by partial transesterification of triglycerides is described in PCT/DE2005/002156. In this case, the fuel yield is 100%, because the glycerol contained in the fats and oils is not liberated, but is kept in solution in the form of mono-, di-, and triglycerides. This mixture of bound glycerol and fatty acid alkylesters is stable at room temperature. At lower temperatures however, below 100C, crystallisation processes are triggered and individual components are precipitated, particularly with the compositions described as especially - 4 advantageous in PCT/DE2005/002156. Consequently, the fuel described in PCT/DE2005/002156 is only suitable for use at room temperature or higher temperatures. The fuel described is therefore not suitable precisely in regions where low temperatures prevail. The object of the present invention consists in providing a biofuel, and a process for production thereof, which may be produced with a high yield and is also usable at lower temperatures. Description of the invention The object is solved with the biofuel according to claim 1 and the process according to claim 13. Advantageous compositions of the biofuel and configurations of the processes for production thereof are described in the subordinate claims or will be evident from the following description and embodiments. The biofuel according to the invention contains at least one fraction of triglycerides, particularly vegetable oil or vegetable fat, and at least one fraction of monoglycerides and at least one fraction of diglycerides, and further contains at least one fraction of alkylesters of fatty acids. Surprisingly, it was found that there is a defined range of compositions with the fractions cited, for which, despite a lower viscosity and higher cetane number, it is possible, by partial transesterification, to keep all of the glycerol contained in the oil in solution in the form of mono-, di and triglycerides, and to store the product even at temperatures below 10C, without demixing or crystallisation. Such demixing does not occur even after the biofuel according to the invention is mixed with diesel fuel, although mixing with diesel does cause the polarity -5 of the mixture to change. Mixtures of the biofuel according to the invention with diesel thus remain clear and monophasic even in wintry conditions. It was found that in order to achieve optimum solubility of glycerides in fatty acid alkylesters (FAAEs) even at lower temperatures, it is critically important that the fraction of FAAEs in the fuel is smaller than the fraction of triglycerides. The triglycerides dissolve particularly readily even at temperatures below 10 0 C if the mass fraction of the triglyceride content is selected to be greater than 29%, advantageously greater than 40%, and the mass fraction of the FAAE is adjusted to greater than 14% and less than 36%. A further factor for increasing the solubility of glycerides in FAAE-containing fuels is the ratio of monoglycerides to diglycerides. If the ratio of diglycerides to monoglycerides is below a value of 2, particles are precipitated particularly rapidly. The following composition contains a mixture of mono-, di-, and triglycerides with FAAE that is particularly advantageous for cold storage: Component Minimum mass % Maximum mass % value value FAAE 15 35 Monoglycerides 0.1 10 Diglycerides 4 30 Triglycerides 30 65 A mixture having a composition of 20-25% by mass FAAE, 50 55% by mass triglycerides, 20% by mass diglycerides, and 5% by mass monoglycerides proved to be particularly stable at low temperatures. A further improvement in terms of low temperature stability may be achieved by adding up to 2% by mass of ethanol. The biofuel may be mixed in any ratio with fossil fuel, biodiesel or BTL-fuel, and in this context it may be diluted and used as fuel for internal combustion engines. It is also possible to dilute the fuel according to the invention by adding diesel fuel or biodiesel before the partial esterification of the triglycerides. It is also expedient to use mono- and diglycerides originating from another reaction in the biofuel, such as those that are formed when vegetable oil is transesterified into fatty acid alkylesters. However, it is also possible, and under certain circumstances may be advantageous, to use mono-, di-, and triglycerides that originate from another source, if applicable from an animal source, or are possibly of synthetic origin. For example, it is possible to use mono- and diglycerides in the biofuel that contain fatty acids with fewer than 10 carbon atoms. One possible production process for the suggested biofuel is based on partial esterification of triglycerides. For this, triglycerides are mixed with an alcohol and a reaction is provoked by adding a catalyst or placing them in contact with a catalyst. The triglycerides used may be a raw material of vegetable, animal or synthetic origin, or mixtures of triglycerides from different sources. The alcohol used is preferably a monovalent alcohol with any chain length. Either organic or inorganic compounds, or enzymes or microorganisms may be used as the catalyst. The reaction may be triggered by homogeneous or heterogeneous catalysis. In a financially particularly advantageous form, used cooking fats serve as the raw material source.
The composition of the biofuel, particularly the ratio of the mass fractions of fatty acid alkylesters and triglycerides and/or the mass fractions of diglycerides relative to the monoglycerides, may be adjusted via the residence time, the type and quantity of catalytic material, and the quantity of alcohol used. In this context, residence time is considered to be the period for which the catalyst and the added alcohol are in contact with the triglycerides. Use of carrier-bound sn-1,3 regiospecific lipases as the catalyst is particularly advantageous. In this context, adding enzymes incrementally over the course of several discontinuous production cycles has proven to produce a particularly good yield. In each production cycle, the enzyme from the previous cycle is used, a small additional quantity of fresh enzyme being added in each cycle to obtain a particularly good yield. It was also discovered that the gradual addition of the alcohol in sub-stoichiometric quantities in several steps or continuous addition of alcohol is particularly advantageous. The gradual or continuous addition of alcohol is to be set up as far as possible so that the concentration of alcohol does not exceed 4% by mass. A maximum alcohol concentration of 3% by mass has proven particularly advantageous for high stability and thus also a long service life of the enzyme. It has also proven advantageous to the same purpose if the alcohol is dissolved in a reaction mixture that is largely free from lipases, and is not brought into contact with the lipases again until the alcohol is completely dissolved. In this context, lipase-free product is removed from the reaction vessel several times during the production cycle for use in dissolving the alcohol that is needed for the reaction. In this way, it is possible to avoid bringing - 8 high alcohol concentrations into contact with the enzyme. In this context it was found that the alcohol concentration in the reaction mixture described should not exceed 5% before it is remixed with the lipase. The process temperature is determined by the catalyst employed, and on the triglyceride used, in particular by the melting point thereof. The residence time is determined by the catalyst employed, the quantity of the catalyst, the alcohol used, and the triglyceride used. Embodiment 2.0 g ethanol are fully dissolved in 100 g rapeseed oil. The transesterification reaction is started by adding 1.0 g of an immobilised s,-1,3 regiospecific lipase. The mixture is mixed thoroughly for 3 hours at the temperature of highest lipase activity. After 3 hours, 50 mL of lipase-free intermediate product is removed from the reaction vessel. 2.0 g of ethanol are completely dissolved in the reaction medium that has been removed. Then, the product-ethanol solution is returned to the reaction vessel. This step is then repeated after a further 3 hours' residence time. After a total of 10 hours, the lipase is separated from the reaction product, and a clear, monophasic liquid is obtained, consisting of 30% by mass fatty acid ethyl ester, 24% by mass diglycerides, 9% by mass monoglycerides, and 36% by mass triglycerides, and about 1% by mass ethanol. The separated enzyme may be reused in a second production cycle. This is performed in identical manner to the cycle described in the preceding. At the start of the reaction, 0.1 g fresh enzyme is added to the enzyme that was used in the first production cycle.
Claims (22)
1. Biofuel that contains at least one fraction of triglycerides, a fraction of monoglycerides, a fraction of diglycerides and a fraction of alkylesters of fatty acids, characterized in that the mass fraction of alkylesters of fatty acids in the biofuel is smaller than the mass fraction of triglycerides.
2. The biofuel according to claim 1, characterized in that the ratio of mass fractions of diglycerides to monoglycerides is > 2.
3. The biofuel according to either of claims 1 or 2, characterized in that the mass fraction of alkylesters of fatty acids is not less than 15% and not more than 35%.
4. The biofuel according to any of claims 1 to 3, characterized in that the mass fraction of triglycerides is at least 30%.
5. The biofuel according to claim 4, characterized in that -2 the mass fraction of triglycerides is greater than 40%.
6. The biofuel according to either of claims 4 or 5, characterized in that the mass fraction of triglycerides is not more than 65%.
7. The biofuel according to any of claims 1 to 6, characterized in that the mass fraction of monoglycerides is between 0.1% and 10%.
8. The biofuel according to any of claims 1 to 7, characterized in that the mass fraction of diglycerides is between 4% and 30%.
9. The biofuel according to claim 1, characterized in that the mass fraction of alkylesters of fatty acids is between 20% and 25%, the mass fraction of triglycerides is between 50% and 55%, the mass fraction of diglycerides is 20%, and the mass fraction of monoglycerides is 5%.
10. The biofuel according to any of claims 1 to 9, characterized in that -3 the biofuel contains an additive of ethanol having a mass fraction of up to 2%.
11. The biofuel according to any of claims 1 to 10, which is mixed with fossil fuel, biodiesel or BTL fuel.
12. Use of the biofuel according to any of the preceding claims as a fuel for internal combustion engines.
13. Process for producing the biofuel according to any of claims 1 to 11 by partial transesterification of triglycerides, wherein at least one fraction each is obtained consisting of triglycerides, monoglycerides, diglycerides, and alkylesters of fatty acids, characterized in that the partial transesterification is carried out in such manner that the mass fraction of alkylesters of fatty acids in the biofuel is smaller than the mass fraction of triglycerides.
14. The process according to claim 13, characterized in that the partial transesterification is carried out in such manner that the ratio of mass fractions of diglycerides to monoglycerides is 2.
15. The process according to either of claims 13 or 14, characterized in that -4 carrier-bound sn-1,3 regiospecific lipases are used as the catalyst for partial transesterification.
16. The process according to claim 15, characterized in that the partial transesterification is completed with gradual addition of enzymes over the course of several discontinuous production cycles.
17. The process according to any of claims 13 to 16, characterized in that alcohol is added in sub-stoichiometric quantity for the transesterification.
18. The process according to claim 17, characterized in that alcohol is added continuously or in several steps during the transesterification.
19. The process according to claim 18, characterized in that when alcohol is added in several steps, an alcohol concentration of 3% by mass is not exceeded.
20. The process according to any of claims 13 to 16, characterized in that - 5 for transesterification, alcohol is first dissolved in a reaction mixture that is largely free from lipases and contains the triglycerides, and that the reaction mixture is not brought into contact with the lipases as the catalyst until the alcohol has been completely dissolved.
21. The process according to claim 20, characterized in that an alcohol concentration of 5% by mass is adjusted in the reaction mixture before it is brought into contact with the lipases.
22. The process according to any of claims 13 to 21, characterized in that the partial transesterification takes place with vegetable oil or vegetable fat as the triglycerides.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102007038232 | 2007-08-13 | ||
| DE102007038232.6 | 2007-08-13 | ||
| PCT/DE2008/001268 WO2009021486A1 (en) | 2007-08-13 | 2008-07-31 | Liquid biofuel made of esters and bound glycerides, and also process for production thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2008286538A1 true AU2008286538A1 (en) | 2009-02-19 |
| AU2008286538B2 AU2008286538B2 (en) | 2012-09-13 |
Family
ID=40155933
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2008286538A Ceased AU2008286538B2 (en) | 2007-08-13 | 2008-07-31 | Liquid biofuel made of esters and bound glycerides, and also process for production thereof |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20110289828A1 (en) |
| EP (1) | EP2183340A1 (en) |
| JP (1) | JP2010535908A (en) |
| KR (1) | KR20100051852A (en) |
| CN (1) | CN101821367A (en) |
| AR (1) | AR067881A1 (en) |
| AU (1) | AU2008286538B2 (en) |
| BR (1) | BRPI0815195A2 (en) |
| CL (1) | CL2008002379A1 (en) |
| DE (1) | DE112008002783A5 (en) |
| MX (1) | MX2010001710A (en) |
| MY (1) | MY156560A (en) |
| RU (1) | RU2010109418A (en) |
| WO (1) | WO2009021486A1 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8585901B1 (en) | 2013-01-25 | 2013-11-19 | Markus Johannes Lenger | Method of continuous in-situ triglyceride stabilization and sulfur reduction of FOG (fats, oil and grease) to optimize fuel extraction |
| EP3344734B1 (en) * | 2015-08-31 | 2022-10-26 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Lubricating mixture having glycerides |
| IT201900014778A1 (en) * | 2019-08-14 | 2021-02-14 | Nextchem S P A | PROCESS FOR THE PRE-TREATMENT OF SUPPLIES INTENDED FOR THE PRODUCTION OF BIO-FUELS, BY MEANS OF HYDROLYSIS OF FATS AT HIGH TEMPERATURE AND PRESSURE |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU5197999A (en) * | 1998-09-01 | 2000-03-21 | Kansai Chemical Engineering Co., Ltd. | Process for producing lower alcohol ester |
| JP2002241786A (en) * | 2000-12-15 | 2002-08-28 | Sumitomo Chem Co Ltd | Method for producing fatty acid ester from seed and/or fruit of plant |
| AU782699B2 (en) * | 2000-12-15 | 2005-08-18 | Sumitomo Chemical Company, Limited | Method for preparing fatty acid esters from seeds or fruits |
| DE102005002700A1 (en) * | 2005-01-19 | 2006-07-27 | Cognis Deutschland Gmbh & Co. Kg | Compositions usable as biofuel |
| FR2914927B1 (en) * | 2007-04-12 | 2009-06-12 | Inst Francais Du Petrole | PROCESS FOR THE PRODUCTION OF ALCOHOLIC ESTERS FROM TRIGLYCERIDES AND ALCOHOLS USING HETEROGENEOUS CATALYSTS BASED ON PHOSPHATE OR ORGANOPHOSPHORUS COMPOUND OF A GROUP 4 METAL. |
-
2008
- 2008-07-31 AU AU2008286538A patent/AU2008286538B2/en not_active Ceased
- 2008-07-31 JP JP2010520417A patent/JP2010535908A/en active Pending
- 2008-07-31 EP EP08801106A patent/EP2183340A1/en not_active Withdrawn
- 2008-07-31 DE DE112008002783T patent/DE112008002783A5/en not_active Ceased
- 2008-07-31 US US12/673,091 patent/US20110289828A1/en not_active Abandoned
- 2008-07-31 BR BRPI0815195 patent/BRPI0815195A2/en not_active IP Right Cessation
- 2008-07-31 CN CN200880103379A patent/CN101821367A/en active Pending
- 2008-07-31 MY MYPI2010000669A patent/MY156560A/en unknown
- 2008-07-31 MX MX2010001710A patent/MX2010001710A/en unknown
- 2008-07-31 WO PCT/DE2008/001268 patent/WO2009021486A1/en active Application Filing
- 2008-07-31 RU RU2010109418/04A patent/RU2010109418A/en unknown
- 2008-07-31 KR KR1020107005225A patent/KR20100051852A/en active IP Right Grant
- 2008-08-07 AR ARP080103462A patent/AR067881A1/en not_active Application Discontinuation
- 2008-08-13 CL CL2008002379A patent/CL2008002379A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2008286538B2 (en) | 2012-09-13 |
| JP2010535908A (en) | 2010-11-25 |
| CN101821367A (en) | 2010-09-01 |
| RU2010109418A (en) | 2011-09-20 |
| US20110289828A1 (en) | 2011-12-01 |
| EP2183340A1 (en) | 2010-05-12 |
| AR067881A1 (en) | 2009-10-28 |
| KR20100051852A (en) | 2010-05-18 |
| MY156560A (en) | 2016-02-26 |
| CL2008002379A1 (en) | 2008-12-19 |
| MX2010001710A (en) | 2010-03-11 |
| WO2009021486A1 (en) | 2009-02-19 |
| BRPI0815195A2 (en) | 2015-03-31 |
| DE112008002783A5 (en) | 2010-07-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Singh et al. | Biodiesel production through the use of different sources and characterization of oils and their esters as the substitute of diesel: a review | |
| Sivakumar et al. | Bio-diesel production by alkali catalyzed transesterification of dairy waste scum | |
| Wahlen et al. | Biodiesel from microalgae, yeast, and bacteria: engine performance and exhaust emissions | |
| Atadashi et al. | The effects of water on biodiesel production and refining technologies: A review | |
| Demirbas | Biodiesel production from vegetable oils via catalytic and non-catalytic supercritical methanol transesterification methods | |
| Cerveró et al. | Production of biodiesel from vegetable oils | |
| KR101290049B1 (en) | Liquid bio-fuel mixture and method and device for producing said mixture | |
| Madiwale et al. | An overview on production, properties, performance and emission analysis of blends of biodiesel | |
| DE102005002700A1 (en) | Compositions usable as biofuel | |
| Manzanera et al. | Biodiesel: An alternative fuel | |
| AU2008286538B2 (en) | Liquid biofuel made of esters and bound glycerides, and also process for production thereof | |
| Nain et al. | Influence of acyl acceptor blends on the ester yield and fuel properties of biodiesel generated by whole-cell catalysis of cottonseed oil | |
| Sidohounde et al. | Transesterification reaction and comparative study of the fuel properties of biodiesels produced from vegetable oils: a review | |
| Casas et al. | Production of biodiesel through interesterification of triglycerides with methyl acetate | |
| Heikal et al. | Jatropha bio-diesel production technologies | |
| Math et al. | Optimization of restaurant waste oil methyl ester yield | |
| Chattopadhyay et al. | Materials and methods for biodiesel production | |
| Ekin | Quality and composition of lipids used in biodiesel production and methods of transesterification: A review | |
| Degife et al. | Extracted Biodiesel as Feed for Internal Combustion Engine | |
| Saxena et al. | Production of biodiesel from various sources | |
| Ju et al. | Biodiesel from rice bran oil | |
| Sharma et al. | A step towards Green Chemistry: Biodiesel | |
| Sumatri et al. | Production of Biodiesel Using Enzymatic Esterification of Multi-Feedstock Oils | |
| Yuan et al. | Chemical conversion process for biodiesel production | |
| Reshad et al. | Production of Biodiesel from Renewable Resources |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |