EP1848787A1 - Melange combustible biologique liquide et procede et dispositif pour le preparer - Google Patents

Melange combustible biologique liquide et procede et dispositif pour le preparer

Info

Publication number
EP1848787A1
EP1848787A1 EP05821059A EP05821059A EP1848787A1 EP 1848787 A1 EP1848787 A1 EP 1848787A1 EP 05821059 A EP05821059 A EP 05821059A EP 05821059 A EP05821059 A EP 05821059A EP 1848787 A1 EP1848787 A1 EP 1848787A1
Authority
EP
European Patent Office
Prior art keywords
bio
fuel mixture
mixture
fuel
fatty acid
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Withdrawn
Application number
EP05821059A
Other languages
German (de)
English (en)
Inventor
Peter Eisner
Andreas STÄBLER
Andreas Malberg
Michael Menner
Michael Frankl
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV
Original Assignee
Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV filed Critical Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV
Publication of EP1848787A1 publication Critical patent/EP1848787A1/fr
Withdrawn legal-status Critical Current

Links

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
    • C10L1/02—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
    • C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • 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
    • 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

Definitions

  • the present invention relates to a liquid biofuel mixture based on fatty acid alkyl ester and a method and an apparatus for producing the same.
  • the fuel is particularly suitable as an additive for conventional fuels such as diesel or gasoline. Direct use of the fuel mixture as fuel for internal combustion engines is also possible.
  • biofuels are understood to mean liquid fuels and fuels which are obtained from renewable raw materials.
  • biofuels are animal fats, vegetable oils and liquids produced from vegetable or animal raw materials, such as fatty acid alkyl esters from the catalytic transesterification of fats and oils, bio-ethanol from the fermentation of
  • Starch Sugar or celluloses but also methanol from the gasification of fat, starch, sugar or cellulose-containing raw materials.
  • biofuels are added today as an additive to conventional fuels such as diesel or petrol to the life cycle assessment of fuels to improve and meet legal requirements.
  • WO 01/29154 A1 describes the direct use of animal fat waste in combustion engines as an economic solution. But it is from the
  • the prior art also discloses that the direct use of renewable fats or oils in internal combustion engines due to the high viscosity and Low cetane number leads to incidents in the combustion process and due to incomplete burn-out to deposits.
  • Bioethanol is obtained through a fermentation process from raw materials contained in plants. Carbohydrates are cleaved with the help of microorganisms and converted to ethanol via several intermediates. Since ethanol still contains at least 5% of water in this process, after the fermentation process an absolute, usually with toluene must be carried out.
  • the ethanol / toluene mixture is commonly referred to as bioethanol and is a substitute for gasoline.
  • bioethanol can not be used in conventional engines.
  • a modification is necessary.
  • the use of a mixture of, usually 95%, gasoline and 5% bioethanol is easily possible.
  • Bioethanol has the benefits of high octane, high combustion efficiency and low emissions.
  • bioethanol is above all the low energy density, the poor life cycle assessment, the low efficiency of the fermentation process and the use of the aromatic toluene.
  • bioethanol as a gasoline additive is both ecologically and economically controversial.
  • Vegetable oils represent a substitute for diesel fuel. They have the best eco-balance of all biofuels and a comparatively high energy density of 38 MJ / kg (diesel: 43 MJ / kg). Nevertheless, oils could not prevail as fuel so far, since the use in diesel engines is technically complex. The most serious problem is the high viscosity of the substances. Because of this, there is an increase in the pump internal pressure and a change in the injection behavior. This can lead to damage to seals, combustion chambers, glow plugs and pistons. In addition, the high viscosity, as well as the low ignitability, can lead to incomplete combustion of the fuel. This leaves oil or grease and combustion residues in the combustion chamber and settle on pistons and nozzles. In addition, it comes to resinification after prolonged use with vegetable oils.
  • Animal fats have the same disadvantages as vegetable oils. However, since animal fats have a much higher viscosity and, moreover, form free fatty acids much faster than is the case with vegetable oils, energetic use only makes sense in heavy oil burners with rotary atomizers.
  • Cetane number can be used in almost all diesel engines of recent design. Biodiesel is biodegradable and does not represent a hazardous substance due to the relatively high flashpoint.
  • Another advantage of the FSAE is the significantly improved emission levels compared to fossil diesel. Above all, the sulfur oxide, the hydrocarbon and the soot particle emissions are significantly reduced. Only the nitrogen oxide output is slightly increased.
  • Another problem is the low winter and oxidation stability of the FSAE.
  • Biodiesel is obtained by catalytic transesterification of vegetable oil.
  • dehydrated, deacidified and degummed oil with a molar excess of alcohol (usually methanol) of 6: 1 using 1 mass percent catalyst (usually KOH) above the boiling point of the alcohol reacted.
  • the fatty acids contained in the fat molecule are catalytically cleaved and react with the present alcohol to fatty acid alkyl esters.
  • Fats and oils are triglycerides, i. a fat molecule contains three fatty acids bound to a glycerol molecule.
  • Transesterification reaction as it is carried out in the production of biodiesel, per molecule of fat or oil, three molecules of biodiesel and one molecule of glycerol.
  • Intermediates of the reaction are mono- and diglycerides.
  • Mono- and diglycerides consist of a glycerol backbone, hereinafter also referred to as glycerol backbone, to which one (monoglyceride) or two (diglyceride) fatty acids are bound. Since both polar hydroxide groups and apolar hydrocarbon chains are present in mono- and diglycerides, they have amphiphilic properties and almost always change the polarity of the solvent in organic solutions.
  • the transesterification requires a reaction time of about 8 hours, with a conversion of about 98% is achieved.
  • the formed, insoluble in FSAE glycerol is removed by means of a phase separator from the biodiesel and used after a chemical and distillative purification as a technical or pharmaceutical raw material.
  • the excess alcohol contained in the FSAE is separated by distillation and returned to the process. Subsequently, the biodiesel is washed with water to remove resulting soaps as well as catalyst and glycerol residues, and dried.
  • the object of the present invention is to provide a bio-fuel mixture and a method and an apparatus for the production thereof, with which the mentioned disadvantages of
  • the bio-fuel mixture should have a lower viscosity than Vegetable oil, so that the fuel can also be used in diesel engines without additional heating and conventional diesel fuel can be added. It should also be liquid and monophasic at low temperatures to achieve a high level of storage stability.
  • bio-fuel mixture according to claim 1 the method according to claims 11 and 21 and the device according to claim 24.
  • Advantageous compositions of the bio-fuel mixture and embodiments of the method and the device for producing the same are the subject of the dependent claims or can be taken from the following description and the exemplary embodiments.
  • the bio-fuel mixture according to the invention contains at least one fraction of fatty acid alkyl ester and a fraction consisting of bound glycerol in the form of mono- and / or diglycerides and / or triglycerides.
  • the proportion of bound glycerol is at least 1 wt .-% in the fuel mixture, based on the glycerol backbone (empirical formula of the glycerol backbone: C3H5O3, molecular weight: 89 g / mol), preferably between 3 and 10 wt .-%. Higher concentrations are possible by adding glycerides and possibly desired.
  • Monoglycerides and / or diglycerides are capable of more than doubling the solubility of free glycerol in FSAE.
  • glycerol separates out as a second phase from the biofuel. This phase has to be separated from the alkyl esters with much effort.
  • the glycerol which is a natural constituent of oils and fats, can be utilized in the bio-fuel mixture according to the invention together with the other fractions in the combustion process.
  • the yield by the co-utilization of glycerol in the fuel thus increases by about 10%, which brings significant cost advantages.
  • the bio-fuel mixture according to the invention is also able to keep more than 40% by weight of fats or oils in solution, and thus to permit co-use of these substances in the fuel mixture, without the need for further phases or separation.
  • the bio-fuel mixture also shows lower exhaust emissions compared to biodiesel with respect to hydrocarbons, carbon monoxide and soot particles.
  • bioethanol is used as alcohol for the transesterification.
  • the bio-fuel mixture can be mixed in any ratio with mineral fuel or conventional biodiesel, thereby diluted and used as a fuel. It is thus possible to set a lower concentration of bound glycerol in the final used fuel.
  • mono- and diglycerides in the bio-fuel mixture, for example, in the Transesterification of vegetable oil to fatty acid alkyl esters are formed.
  • mono-, di- and triglycerides which originate from another source or are of synthetic origin.
  • mono- and diglycerides can be used in the bio-fuel mixture containing fatty acids with less than 10 carbon atoms in the fatty acid molecule. This can bring particular advantages for reducing the viscosity.
  • One possible method of preparation is based on a partial transesterification of triglycerides.
  • purified and possibly dehydrated fat or oil is mixed with a monohydric alcohol and reacted by addition of a suitable catalyst.
  • a suitable catalyst for this purpose, the fat, oil, alcohol and catalyst can also be mixtures of different substances.
  • the ratio of FSAE, mono-, di- and optionally triglycerides can be adjusted in the reaction product.
  • the catalysts used are preferably one or more regiospecific lipases. Particularly advantageous is the use of S n -1, 3 regiospecific lipases as a catalyst.
  • Such lipases Preferably, the first and third fatty acids cleave from the tricylceride.
  • a mixture of mono- and diglycerides is formed along with FSAE.
  • alcohol consumption was reduced by 33-50% compared to conventional biodiesel production, since the alcohol glycerol remains in the bio-fuel mixture and does not have to be substituted.
  • the catalyst or the catalyst mixture can be present both in free form and as a carrier-bound system.
  • Supported catalysts have the advantage that they can be used over several reaction cycles. This is due to the relatively high price, especially in the use of lipases as a catalyst advantage.
  • the device proposed for producing the biofuel has a reactor for receiving the mixture, which contains one or more carriers with one or more immobilized regiospecific lipases. This may be, for example, a stirred reactor or a fixed bed reactor.
  • the reactor is followed by a separator for separating a bound fraction containing glycerol and / or alcohol from the product obtained by the reaction.
  • This separated fraction is preferably returned to the mixing device so that no waste products are formed during the production process. It is also possible to supply the separated fraction to a separate recycling.
  • the separating device may be, for example, a distillative separation device or a membrane separation device or a crystallization separation device or an adsorption separation device or extraction separation device.
  • the process temperature for producing the biofuel mixture depends on the catalyst used and the triglyceride used. However, it usually moves between 20 and 120 ° C.
  • the reaction rate depends on the catalyst concentration and the catalyst used.
  • the reaction time or residence time is chosen depending on the desired fuel properties.
  • the removal of water during the transesterification process also has the advantage that the formation of free fatty acids is reduced.
  • a downstream cleaning of the fuel is not necessary, except for the removal of the free or carrier-bound catalyst.
  • it can be carried out to adapt certain properties, such as increasing the viscosity by removing the residual alcohol.
  • it may be advantageous to separate parts of the bound glycerol from the fuel mixture to adjust a lower viscosity. This can be achieved by means of prior art methods such as e.g. by membrane process, crystallization, adsorption or extraction e.g. with water or other polar or amphiphilic liquids.
  • the biofuel mixture can also by addition of mono- and diglycerides, optionally also alcohols and
  • Triglycerides to pure, i. commercially available, FSAE be obtained.
  • the proportions of the glycerides and alcohols used depend on the desired properties.
  • a high FSAE content of> 50% by weight is advantageous, particularly advantageously> 60% by weight, in some cases also> 80% by weight.
  • a high FSAE content preferably of> 50% by weight
  • a high monoglyceride content preferably of> 25% by weight, should be aimed for.
  • the proportion of residual fat should be as low as possible, preferably ⁇ 2 wt .-% for this application.
  • the fuel contains both mono- and diglycerides.
  • monoglycerides e.g. it can come to the crystallization of monoglycerides.
  • di- and / or triglycerides inhibits the
  • the fuel based on alkyl esters is shown below in two examples.
  • fatty acid methyl ester biodiesel
  • This glyceride mixture can be purchased commercially.
  • the bio-fuel mixture can be used as fuel.
  • the figure shows highly schematic components of an exemplary apparatus for producing the bio-fuel mixture and the interaction of these components in the manufacturing process.
  • triglycerides and alcohol are added to a mixer 1 and mixed therein. The mix out
  • Triglycerides and alcohol are then transferred to a stirred or fixed bed reactor 2. This can be done via a connecting line between the mixing device and the reactor 2.
  • the mixture is contacted with sn-1,3 regiospecific lipases as a catalyst to achieve partial transesterification.
  • the regiospecific lipases are present in immobilized form on one or more carriers in the reactor.
  • the product of the reaction is a mixture of fatty acid alkyl esters and monoglycerides, which may optionally also contain di- and triglycerides.
  • a separation device 3 which is optionally downstream of the reactor 2, a residue of alcohol and triglycerides can be separated from the reaction product by distillation or by means of membrane separation technology and fed again to the process at the mixing device 1.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • Health & Medical Sciences (AREA)
  • Biotechnology (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)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)

Abstract

La présente invention concerne un mélange combustible biologique qui se compose d'une fraction d'ester d'alkyle d'acide gras et d'au moins une fraction de glycérine liée, avec une proportion supérieure ou égale à 1 % en poids rapportés au squelette de la glycérine, ainsi qu'un procédé et un dispositif pour préparer le mélange combustible biologique. Le mélange combustible biologique peut être préparé de façon économique, peut être utilisé en tant que combustible même dans des moteurs diesel sans nécessiter de chauffage supplémentaire, et peut être mélangé avec du carburant diesel conventionnel.
EP05821059A 2005-02-17 2005-11-30 Melange combustible biologique liquide et procede et dispositif pour le preparer Withdrawn EP1848787A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102005007369 2005-02-17
PCT/DE2005/002156 WO2006086936A1 (fr) 2005-02-17 2005-11-30 Melange combustible biologique liquide et procede et dispositif pour le preparer

Publications (1)

Publication Number Publication Date
EP1848787A1 true EP1848787A1 (fr) 2007-10-31

Family

ID=35966989

Family Applications (1)

Application Number Title Priority Date Filing Date
EP05821059A Withdrawn EP1848787A1 (fr) 2005-02-17 2005-11-30 Melange combustible biologique liquide et procede et dispositif pour le preparer

Country Status (16)

Country Link
US (1) US20090203092A1 (fr)
EP (1) EP1848787A1 (fr)
JP (1) JP5072605B2 (fr)
KR (1) KR101290049B1 (fr)
CN (1) CN101184826A (fr)
AR (1) AR053801A1 (fr)
AU (1) AU2005327879B2 (fr)
BR (1) BRPI0520104A (fr)
CA (1) CA2597679A1 (fr)
DE (1) DE112005003550A5 (fr)
EG (1) EG24718A (fr)
MA (1) MA29308B1 (fr)
MX (1) MX2007009954A (fr)
NO (1) NO20074212L (fr)
WO (1) WO2006086936A1 (fr)
ZA (1) ZA200706614B (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102006002848A1 (de) * 2006-01-19 2007-07-26 Dracowo Forschungs- Und Entwicklungs Gmbh Herstellung von Fettsäuremethylestern aus Altfetten und Ölen mittels Biodieselkleinstanlage
EP1918354A1 (fr) * 2006-10-13 2008-05-07 Cognis Oleochemicals GmbH Compositions de combustible comprenant de la glycérine
ES2433072T3 (es) * 2007-02-06 2013-12-09 János Thész Uso de fueles o aditivos de fuel basados en triglicéridos de estructura modificada
EP2121875A1 (fr) * 2007-02-26 2009-11-25 The Petroleum Oil and Gas Corporation of South Africa Carburants à base de biodiesel
BRPI0701993A2 (pt) * 2007-03-30 2008-11-18 Petroleo Brasileiro Sa mÉtodo para reciclagem e aproveitamento da glicerina obtida da produÇço do biodiesel
EP2065460A1 (fr) * 2007-11-28 2009-06-03 Wulfenia Beteiligungs GmbH Combustible biologique et son procédé de fabrication
KR100948292B1 (ko) * 2007-11-30 2010-03-17 제이씨케미칼(주) 바이오디젤 제조용 다단 반응기 시스템
WO2010118891A1 (fr) * 2009-04-17 2010-10-21 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Liquide lubrifiant, et procédé pour sa fabrication
KR20100136060A (ko) * 2009-06-18 2010-12-28 서강오씨아이 주식회사 바이오디젤 부산물을 이용한 바이오디젤 제조방법
US8974553B2 (en) 2012-03-29 2015-03-10 Joseph Ried Miscible diesel fuel ethanol composition
EP2657324A1 (fr) 2012-04-26 2013-10-30 Petróleo Brasileiro S.A. - PETROBRAS Procédé pour la production de lubrifiant biologique à partir de biodiesel méthylique et lubrifiant bio obtenu par ledit procédé
CN106480114B (zh) * 2015-08-25 2021-10-08 丰益(上海)生物技术研发中心有限公司 制备生物柴油的方法
IT201900014778A1 (it) * 2019-08-14 2021-02-14 Nextchem S P A Processo per il pretrattamento di alimentazioni destinate alla produzione di bio-carburanti, mediante idrolisi di grassi ad alta temperatura e pressione
GB202005461D0 (en) * 2020-04-15 2020-05-27 Trio Plus Bio Energy Ag Additive

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5316927A (en) * 1988-10-04 1994-05-31 Opta Food Ingredients, Inc. Production of monoglycerides by enzymatic transesterification
JP2668187B2 (ja) * 1993-09-17 1997-10-27 日清製油株式会社 リパーゼ粉末を用いたエステル交換法
US5578090A (en) * 1995-06-07 1996-11-26 Bri Biodiesel fuel
US5713965A (en) * 1996-04-12 1998-02-03 The United States Of America As Represented By The Secretary Of Agriculture Production of biodiesel, lubricants and fuel and lubricant additives
DE19702989A1 (de) * 1997-01-28 1998-07-30 Clariant Gmbh Umweltfreundlicher Dieseltreibstoff
KR100644918B1 (ko) * 1997-11-24 2006-11-10 에네르게아 움벨트테크놀로지 게엠베하 지방산 메틸 에스테르 제조 방법 및 그를 실현하기 위한장치
CA2336513C (fr) * 2000-02-17 2010-08-24 Tatsuo Tateno Methode de production d'esters d'acide gras et combustibles contenant un ester d'acide gras
JP4556268B2 (ja) 2000-02-17 2010-10-06 住友化学株式会社 脂肪酸エステルの製造方法
AU782699B2 (en) * 2000-12-15 2005-08-18 Sumitomo Chemical Company, Limited Method for preparing fatty acid esters from seeds or fruits
CN1238469C (zh) * 2004-01-16 2006-01-25 清华大学 有机介质反应体系中脂肪酶转化油脂生产生物柴油新工艺
DE102005002700A1 (de) * 2005-01-19 2006-07-27 Cognis Deutschland Gmbh & Co. Kg Zusammensetzungen verwendbar als Biotreibstoff
FR2914927B1 (fr) * 2007-04-12 2009-06-12 Inst Francais Du Petrole Procede de fabrication d'esters alcooliques a partir de triglycerides et d'alcools au moyens de catalyseurs heterogenes a base de phosphate ou de compose organophosphore d'un metal du groupe 4.

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2006086936A1 *

Also Published As

Publication number Publication date
MA29308B1 (fr) 2008-03-03
JP2008530318A (ja) 2008-08-07
CN101184826A (zh) 2008-05-21
NO20074212L (no) 2007-09-17
US20090203092A1 (en) 2009-08-13
MX2007009954A (es) 2007-09-26
DE112005003550A5 (de) 2008-01-24
KR101290049B1 (ko) 2013-07-30
KR20070114132A (ko) 2007-11-29
WO2006086936A1 (fr) 2006-08-24
AU2005327879A1 (en) 2006-08-24
CA2597679A1 (fr) 2006-08-24
EG24718A (en) 2010-06-07
AR053801A1 (es) 2007-05-23
AU2005327879B2 (en) 2011-03-03
BRPI0520104A (pt) 2008-06-10
JP5072605B2 (ja) 2012-11-14
ZA200706614B (en) 2008-04-30

Similar Documents

Publication Publication Date Title
WO2006086936A1 (fr) Melange combustible biologique liquide et procede et dispositif pour le preparer
DE3150989C2 (fr)
EP1838822A2 (fr) Compositions pouvant etre utilisees comme biocarburant
DE10243700A1 (de) Verfahren und Vorrichtung zur Herstellung von Biodiesel
DE3149170A1 (de) Brennbare komposition, welche gasoel, methanol und einen fettsaeureester enthalten und als dieseltreibstoff brauchbar sind
DE102006019763B4 (de) Verfahren zur Gewinnung von Brennstoffen aus pflanzlichen und tierischen Fettabfällen sowie Anlage zur Durchführung des Verfahrens
DE3150988C2 (fr)
DE102006044467B4 (de) Verfahren zur kontinuierlichen Herstellung von Fettsäure-Methylester oder Fettsäure-Ethylester
EP1908815A2 (fr) Carburant et mélanges de carburants avec des hydrocarbures synthétiques à partie élevée d'isoparaffine
EP2358851B2 (fr) Utilisation de l'acide méthanesulfonique pour la fabrication d'esters d'acide gras
WO2010112158A1 (fr) Esters de l'acide citrique, servant de carburants et combustibles de chauffage biogènes, renouvelables
AT504745B1 (de) Schwefelarmer dieseltreibstoff sowie verwendung von fettsäuremonoalkylestern als schmierfähigkeitsverbesserer für schwefelarme dieseltreibstoffe
Jonnalagadda et al. Experimental investigation on the production of linseed biodiesel yielding and properties evaluation
EP2183340A1 (fr) Biocarburant liquide issu d'esters et de glycérides liés, ainsi que son procédé de production
AT412280B (de) Gereinigter fettsäurealkylester mit niedrigem schwefelgehalt und verfahren zu seiner herstellung
WO2010037772A1 (fr) Procédé de fabrication d'un biodiesel
DE102011116020B4 (de) Verfahren zur Herstellung von synthetischen Diesel-, Benzin- und Kerosinkomponenten aus Algen
AT398777B (de) Verfahren zur reinigung von rohen pflanzenölestern
AT502540B1 (de) Verfahren zur herstellung eines treibstoffes oder treibstoffzusatzes und treibstoff bzw. treibstoffzusatz
DE102009044168A1 (de) Verfahren und Vorrichtung zur kontinuierlichen Herstellung von Alkylestern höherer Fettsäuren
NURUL'ADILAH Combination of Mussel Shell and Potassium Hydroxide as Solid Waste Basic Catalyst (SWBC) for Fatty Acid Methyl Ester (FAME) Synthesis from Castor Oil
WO2009030417A1 (fr) Procédé et dispositif de fabrication d'un carburant biodiesel

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20070810

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: YU

RIN1 Information on inventor provided before grant (corrected)

Inventor name: FRANKL, MICHAEL

Inventor name: MENNER, MICHAEL

Inventor name: MALBERG, ANDREAS

Inventor name: STAEBLER, ANDREAS

Inventor name: EISNER, PETER

RAX Requested extension states of the european patent have changed

Extension state: YU

Payment date: 20070810

17Q First examination report despatched

Effective date: 20100310

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20130601