ZA200602864B - Method for producing hydrocarbons and oxygen-containing compounds, from biomass - Google Patents
Method for producing hydrocarbons and oxygen-containing compounds, from biomass Download PDFInfo
- Publication number
- ZA200602864B ZA200602864B ZA200602864A ZA200602864A ZA200602864B ZA 200602864 B ZA200602864 B ZA 200602864B ZA 200602864 A ZA200602864 A ZA 200602864A ZA 200602864 A ZA200602864 A ZA 200602864A ZA 200602864 B ZA200602864 B ZA 200602864B
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- South Africa
- Prior art keywords
- alcohols
- mixture
- fermentation
- hydrocarbons
- saturated
- Prior art date
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Classifications
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- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
- C07C1/24—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms by elimination of water
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- C07C29/177—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrogenation of carbon-to-carbon double or triple bonds with simultaneous reduction of a carboxy group
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/49—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide
- C07C45/50—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
- C07C45/505—Asymmetric hydroformylation
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
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- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/02—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
- C07C5/03—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of non-aromatic carbon-to-carbon double bonds
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- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
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- C12P7/00—Preparation of oxygen-containing organic compounds
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- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
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- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/06—Ethanol, i.e. non-beverage
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- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/16—Butanols
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- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/18—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic polyhydric
-
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- C12P7/00—Preparation of oxygen-containing organic compounds
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- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/54—Acetic acid
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- 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
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US51358303P | 2003-10-24 | 2003-10-24 | |
SE0302800A SE526429C2 (sv) | 2003-10-24 | 2003-10-24 | Metod för att framställa syreinnehållande föreningar utgående från biomassa |
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CN (1) | CN100396779C (hu) |
AU (1) | AU2004284364B2 (hu) |
BR (1) | BRPI0415619B1 (hu) |
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CU (1) | CU23839B1 (hu) |
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ES (1) | ES2774700T3 (hu) |
HK (1) | HK1096428A1 (hu) |
HR (1) | HRP20200323T1 (hu) |
HU (1) | HUE048539T2 (hu) |
IL (1) | IL174793A (hu) |
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SI (1) | SI1680509T1 (hu) |
UA (1) | UA84299C2 (hu) |
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Families Citing this family (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7074603B2 (en) * | 1999-03-11 | 2006-07-11 | Zeachem, Inc. | Process for producing ethanol from corn dry milling |
PL207932B1 (pl) * | 1999-03-11 | 2011-02-28 | Zeachem Inc | Sposób wytwarzania etanolu |
MX306561B (es) * | 2004-01-29 | 2013-01-09 | Zeachem Inc | Recuperacion de acidos organicos. |
US20150328347A1 (en) | 2005-03-24 | 2015-11-19 | Xyleco, Inc. | Fibrous materials and composites |
US7708214B2 (en) | 2005-08-24 | 2010-05-04 | Xyleco, Inc. | Fibrous materials and composites |
US20070014895A1 (en) * | 2005-07-12 | 2007-01-18 | Holtzapple Mark T | System and Method for Converting Biomass |
US8945899B2 (en) | 2007-12-20 | 2015-02-03 | Butamax Advanced Biofuels Llc | Ketol-acid reductoisomerase using NADH |
US8273558B2 (en) | 2005-10-26 | 2012-09-25 | Butamax(Tm) Advanced Biofuels Llc | Fermentive production of four carbon alcohols |
US8450542B2 (en) | 2005-12-16 | 2013-05-28 | Phillips 66 Company | Integrated process for converting carbohydrates to hydrocarbons |
US7678950B2 (en) | 2005-12-16 | 2010-03-16 | Conocophillips Company | Process for converting carbohydrates to hydrocarbons |
US20080015395A1 (en) * | 2006-06-16 | 2008-01-17 | D Amore Michael B | Process for making butenes from aqueous 1-butanol |
US20080015396A1 (en) * | 2006-06-16 | 2008-01-17 | D Amore Michael B | Process for making dibutyl ethers from dry isobutanol |
US20080045754A1 (en) * | 2006-06-16 | 2008-02-21 | D Amore Michael B | Process for making butenes from dry 1-butanol |
US8975047B2 (en) * | 2006-06-16 | 2015-03-10 | E I Du Pont De Nemours And Company | Process for making isooctenes from dry 1-butanol |
US20080009656A1 (en) * | 2006-06-16 | 2008-01-10 | D Amore Michael B | Process for making isooctenes from dry isobutanol |
US20080015397A1 (en) * | 2006-06-16 | 2008-01-17 | D Amore Michael B | Process for making isooctenes from aqueous 1-butanol |
US20090099401A1 (en) | 2006-06-16 | 2009-04-16 | D Amore Michael B | Process for making isooctenes from aqueous isobutanol |
US20080132741A1 (en) * | 2006-06-16 | 2008-06-05 | D Amore Michael B | Process for making butenes from dry isobutanol |
US20090030239A1 (en) * | 2006-06-16 | 2009-01-29 | D Amore Michael B | Process for making butenes from aqueous isobutanol |
AP2724A (en) | 2006-07-21 | 2013-08-31 | Xyleco Inc | Conversion systems for biomass |
JP5013396B2 (ja) * | 2006-09-01 | 2012-08-29 | 独立行政法人産業技術総合研究所 | 炭素数3の多価アルコールの脱水/水素化用触媒及びそれを用いた炭化水素の製造方法 |
US7915470B2 (en) | 2006-09-08 | 2011-03-29 | Board Of Regents, The University Of Texas System | Coupled electrochemical method for reduction of polyols to hydrocarbons |
US8521310B2 (en) * | 2006-10-31 | 2013-08-27 | Rockwell Automation Technologies, Inc. | Integrated model predictive control of distillation and dehydration sub-processes in a biofuel production process |
US7933849B2 (en) * | 2006-10-31 | 2011-04-26 | Rockwell Automation Technologies, Inc. | Integrated model predictive control of batch and continuous processes in a biofuel production process |
US7831318B2 (en) * | 2006-10-31 | 2010-11-09 | Rockwell Automation Technologies, Inc. | Model predictive control of fermentation temperature in biofuel production |
US8571690B2 (en) * | 2006-10-31 | 2013-10-29 | Rockwell Automation Technologies, Inc. | Nonlinear model predictive control of a biofuel fermentation process |
US20080103747A1 (en) * | 2006-10-31 | 2008-05-01 | Macharia Maina A | Model predictive control of a stillage sub-process in a biofuel production process |
US8634940B2 (en) * | 2006-10-31 | 2014-01-21 | Rockwell Automation Technologies, Inc. | Model predictive control of a fermentation feed in biofuel production |
JP2010030902A (ja) * | 2006-11-21 | 2010-02-12 | Mitsui Chemicals Inc | エチレンの製造方法 |
US20080132732A1 (en) * | 2006-12-01 | 2008-06-05 | Leo Ernest Manzer | Process for making butenes from aqueous 2-butanol |
US20080132730A1 (en) * | 2006-12-01 | 2008-06-05 | Leo Ernest Manzer | Process for making butenes from dry 2-butanol |
US20080131948A1 (en) * | 2006-12-01 | 2008-06-05 | Leo Ernest Manzer | Process for making isooctenes from dry 2-butanol |
US20080234523A1 (en) * | 2006-12-01 | 2008-09-25 | Leo Ernest Manzer | Process for making isooctenes from aqueous 2-butanol |
BRPI0605173A (pt) * | 2006-12-05 | 2008-07-22 | Braskem Sa | processo de produção de uma ou mais olefinas, olefina, e, polìmero |
EP2121946A4 (en) * | 2007-02-09 | 2012-08-29 | Zeachem Inc | ENERGY-EFFICIENT METHOD FOR MANUFACTURING PRODUCTS |
BRPI0701993A2 (pt) * | 2007-03-30 | 2008-11-18 | Petroleo Brasileiro Sa | mÉtodo para reciclagem e aproveitamento da glicerina obtida da produÇço do biodiesel |
US7910342B2 (en) | 2007-04-18 | 2011-03-22 | Butamax(Tm) Advanced Biofuels Llc | Fermentive production of isobutanol using highly active ketol-acid reductoisomerase enzymes |
US8153850B2 (en) * | 2007-05-11 | 2012-04-10 | The Texas A&M University System | Integrated biofuel production system |
EP2167452A1 (en) * | 2007-06-25 | 2010-03-31 | Mcneff Research Consultants, Inc. | Catalysts, systems and methods for ether synthesis |
RU2486235C2 (ru) * | 2007-06-27 | 2013-06-27 | Новозимс А/С | Способ получения продуктов ферментации |
EP2017346A1 (en) * | 2007-07-19 | 2009-01-21 | Ineos Europe Limited | Process for the production of alcohols |
RU2459857C2 (ru) | 2007-07-20 | 2012-08-27 | Юпм-Киммене Ойй | Способ и устройство для получения жидкого биотоплива из твердой биомассы |
US9145566B2 (en) * | 2007-07-27 | 2015-09-29 | Swift Fuels, Llc | Renewable engine fuel and method of producing same |
UA98002C2 (uk) * | 2007-09-07 | 2012-04-10 | Фураникс Технолоджиз Б.В. | Спосіб одержання суміші похідних фурфуралю і 5-алкоксиметилфурфуралю та паливо, що містить таку суміш |
US8193402B2 (en) * | 2007-12-03 | 2012-06-05 | Gevo, Inc. | Renewable compositions |
EP2225351A4 (en) | 2007-12-03 | 2016-11-09 | Gevo Inc | RENEWABLE COMPOSITIONS |
ATE528329T1 (de) * | 2007-12-05 | 2011-10-15 | Braskem Sa | Integriertes verfahren zur herstellung eines ethylen-butylen-copolymers, ethylen-butylen- copolymer und verwendung von ethylen und 1- butylen als aus erneuerbaren natürlichen rohmaterialien gewonnene comonomere |
ES2575413T3 (es) | 2007-12-20 | 2016-06-28 | Butamax (Tm) Advanced Biofuels Llc | Cetol-ácido reductoisomerasa que utiliza NADH |
KR20100107480A (ko) * | 2007-12-27 | 2010-10-05 | 게보 인코포레이티드 | 묽은 수용액으로부터 고급 알콜들의 회수 |
WO2009091783A2 (en) * | 2008-01-14 | 2009-07-23 | Pennsylvania Sustainable Technologies, Llc | Method and system for producing alternative liquid fuels or chemicals |
US7932297B2 (en) | 2008-01-14 | 2011-04-26 | Pennsylvania Sustainable Technologies, Llc | Method and system for producing alternative liquid fuels or chemicals |
MX2010008587A (es) * | 2008-02-07 | 2010-09-28 | Zeachem Inc | Produccion indirecta de butanol y hexanol. |
KR100970936B1 (ko) * | 2008-04-25 | 2010-07-20 | 한국에너지기술연구원 | 가스화장치를 이용한 바이오디젤 정제 잔여물의 가스화방법 |
NZ588804A (en) * | 2008-05-07 | 2012-03-30 | Zeachem Inc | Recovery of organic acids |
FR2931477B1 (fr) * | 2008-05-21 | 2012-08-17 | Arkema France | Acide cyanhydrique derive de matiere premiere renouvable |
FR2934264B1 (fr) * | 2008-07-22 | 2012-07-20 | Arkema France | Fabrication d'esters de vinyle a partir de matieres renouvelables, esters de vinyle obtenus et utilisations |
FR2934261B1 (fr) * | 2008-07-25 | 2015-04-10 | Arkema France | Procede de synthese d'esters de l'acide acrylique |
FR2938535B1 (fr) * | 2008-11-20 | 2012-08-17 | Arkema France | Procede de fabrication de methylmercaptopropionaldehyde et de methionine a partir de matieres renouvelables |
FR2938838B1 (fr) * | 2008-11-27 | 2012-06-08 | Arkema France | Procede de fabrication d'un methacrylate de methyle derive de la biomasse |
WO2010075437A2 (en) * | 2008-12-22 | 2010-07-01 | Sartec Corporation | Systems and methods for producing fuels and fuel precursors from carbohydrates |
FR2940801B1 (fr) * | 2009-01-06 | 2012-08-17 | Arkema France | Procede de fabrication d'un methacrylate de methyle derive de la biomasse |
NZ730533A (en) | 2009-01-26 | 2018-09-28 | Xyleco Inc | Processing biomass |
US20100216958A1 (en) * | 2009-02-24 | 2010-08-26 | Peters Matthew W | Methods of Preparing Renewable Butadiene and Renewable Isoprene |
PL2403894T3 (pl) * | 2009-03-03 | 2016-12-30 | Opakowanie pochodzenia biologicznego z politereftalanu etylenu i sposób jego produkcji | |
FR2945543B1 (fr) * | 2009-05-15 | 2011-05-06 | Inst Francais Du Petrole | Procede de production d'alcools et/ou de solvants a partir de biomasse lignocellulosique avec recyclage acide des residus solides |
WO2010148348A2 (en) * | 2009-06-19 | 2010-12-23 | The Texas A&M University System | Integrated biofuel processing system |
BR112012016042A2 (pt) | 2009-12-29 | 2020-09-15 | Butamax Advanced Biofuels Llc | "celula hospedeira microbiana recombinante, metodo para a produção de isobutanol, método para a produção de 2-butanol e método para a produção de 14-butanol |
KR101664450B1 (ko) * | 2010-01-08 | 2016-10-11 | 한국과학기술원 | 바이오매스로부터 유기산을 생산하는 방법 |
MY159813A (en) | 2010-01-08 | 2017-02-15 | Gevo Inc | Integrated methods of preparing renewable chemicals |
WO2011139711A2 (en) * | 2010-04-26 | 2011-11-10 | Terrabon, Inc. | Anaerobic organisms in a process for converting biomass |
US8373012B2 (en) | 2010-05-07 | 2013-02-12 | Gevo, Inc. | Renewable jet fuel blendstock from isobutanol |
KR101089488B1 (ko) | 2010-07-14 | 2011-12-02 | 주식회사 엘지화학 | 올레핀으로부터 이소타입의 알데히드와 알콜의 병산 장치 및 이를 이용한 병산 방법 |
CN103827304B (zh) | 2011-03-24 | 2018-04-17 | 布特马斯先进生物燃料有限责任公司 | 用于异丁醇生产的宿主细胞和方法 |
TW201247596A (en) | 2011-04-19 | 2012-12-01 | Gevo Inc | Variations on prins-like chemistry to produce 2,5-dimethylhexadiene from isobutanol |
FR2976293B1 (fr) * | 2011-06-10 | 2015-01-02 | Arkema France | Procede de synthese de composes hydrocarbones bi-fonctionnels a partir de biomasse |
US8871051B2 (en) | 2012-03-21 | 2014-10-28 | Los Alamos National Security, Llc | Process for decomposing lignin in biomass |
BR112014028153A2 (pt) | 2012-05-11 | 2018-05-08 | Butamax Advanced Biofuels Llc | polipeptídeo , célula hospedeira , método para a conversão de acetolactato e de produção de um produto e composição. |
WO2014047421A1 (en) | 2012-09-21 | 2014-03-27 | Butamax(Tm) Advanced Biofuels Llc | Production of renewable hydrocarbon compositions |
JP6407869B2 (ja) | 2012-09-26 | 2018-10-17 | ビュータマックス・アドバンスド・バイオフューエルズ・エルエルシー | ケトール酸レダクトイソメラーゼ活性を有するポリペプチド |
US9914672B2 (en) | 2012-10-19 | 2018-03-13 | Lummus Technology Inc. | Conversion of alcohols to distillate fuels |
FR2997397B1 (fr) * | 2012-10-29 | 2014-11-07 | Arkema France | Procede de synthese directe d'aldehydes insatures a partir de melanges d'alcools |
KR101450089B1 (ko) | 2012-12-20 | 2014-10-15 | 한국과학기술연구원 | 산-금속 복합촉매를 이용하여 벤질페닐에테르를 포함하는 바이오매스로부터 고탄소의 포화탄화수소를 생산하는 방법 |
US8889386B2 (en) | 2013-04-11 | 2014-11-18 | Hankyong Industry Academic Cooperation Center | Method for producing bio-alcohol using nanoparticles |
BR102013022434B8 (pt) * | 2013-09-02 | 2022-06-21 | Advel Tecnologia E Comercio Eireli | Processo para fermentação microbiana de substratos açucarados |
FR3019545B1 (fr) | 2014-04-04 | 2016-03-11 | Arkema France | Procede de synthese directe de (meth)acroleine a partir d'ethers et/ou acetals |
US20170051237A1 (en) * | 2014-05-15 | 2017-02-23 | Ihi Enviro Corporation | Plant processing system |
EP3144368A4 (en) * | 2014-05-15 | 2017-11-22 | IHI Enviro Corporation | Liquid fuel production method using biomass |
DE102015002830B4 (de) | 2015-03-05 | 2019-05-23 | Hochschule Furtwangen | Bioraffinerie-Verfahren |
WO2016194727A1 (ja) * | 2015-05-29 | 2016-12-08 | 横浜ゴム株式会社 | 老化防止剤の製造方法 |
RU2731511C2 (ru) * | 2015-06-23 | 2020-09-03 | Минн-Дак Фармерз Кооперэтив | Способ автолиза дрожжей, усиленного сапонином |
US10239812B2 (en) | 2017-04-27 | 2019-03-26 | Sartec Corporation | Systems and methods for synthesis of phenolics and ketones |
AU2018309697A1 (en) * | 2017-07-31 | 2020-02-20 | Synata Bio, Inc. | System and method for concentrating suspended solids prior to removal |
CN108244628A (zh) * | 2018-01-18 | 2018-07-06 | 路传章 | 一种富含多肽-金属螯合物的营养液及其制备方法和应用 |
US10544381B2 (en) | 2018-02-07 | 2020-01-28 | Sartec Corporation | Methods and apparatus for producing alkyl esters from a reaction mixture containing acidified soap stock, alcohol feedstock, and acid |
US10696923B2 (en) | 2018-02-07 | 2020-06-30 | Sartec Corporation | Methods and apparatus for producing alkyl esters from lipid feed stocks, alcohol feedstocks, and acids |
CN112739678A (zh) | 2018-09-17 | 2021-04-30 | 埃克森美孚化学专利公司 | 用于生产含氧化合物的转移加氢甲酰化 |
KR102272012B1 (ko) * | 2019-11-06 | 2021-07-01 | 세종대학교산학협력단 | 혐기성소화조의 중간생성물을 이용한 바이오알코올의 제조방법 |
FI4141090T3 (fi) * | 2021-08-31 | 2023-11-10 | Swedish Biofuels Ab | Menetelmä moottoripolttoaineen tuottamiseksi etanolista |
IT202200004013A1 (it) * | 2022-03-03 | 2023-09-03 | Milano Politecnico | Processo autosostenibile a zero emissioni per produzione di chemicals da fonti organiche |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1725084A (en) * | 1927-11-08 | 1929-08-20 | Eastern Alcohol Corp | Process of producing fusel oil by fermentation |
US2272982A (en) * | 1938-07-19 | 1942-02-10 | Owen William Ludwell | Process for increasing fermentative efficiency in ethanol production |
US4066793A (en) * | 1974-03-18 | 1978-01-03 | Ajinomoto Co., Inc. | Seasoning composition and preparation thereof |
US4342831A (en) * | 1979-07-02 | 1982-08-03 | American Can Company | Fermentable acid hydrolyzates and fermentation process |
US4326032A (en) * | 1979-08-20 | 1982-04-20 | Grove Leslie H | Process for the production of organic fuel |
DE3303571C2 (de) * | 1982-03-11 | 1984-07-26 | Buckau-Walther AG, 4048 Grevenbroich | Verfahren und Anlage zur Herstellung von Äthanol |
US4571384A (en) * | 1982-10-18 | 1986-02-18 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University | Methane production |
ZA838867B (en) * | 1982-12-01 | 1984-07-25 | Thomas Anthony Carson | Fermentation method and composition for use therein |
JPS6317696A (ja) * | 1986-07-08 | 1988-01-25 | Shinenerugii Sogo Kaihatsu Kiko | アルコ−ルの発酵方法 |
US5173429A (en) * | 1990-11-09 | 1992-12-22 | The Board Of Trustees Of The University Of Arkansas | Clostridiumm ljungdahlii, an anaerobic ethanol and acetate producing microorganism |
US5070016A (en) * | 1991-03-28 | 1991-12-03 | Revolution Fuels Of America, Inc. | Integrated process for producing ethanol, methanol and butyl ethers |
US6265619B1 (en) * | 1996-01-17 | 2001-07-24 | Exxon Chemical Patents Inc. | Oxygenates and processes for their manufacture |
US6130076A (en) * | 1997-06-19 | 2000-10-10 | University Of Florida Research Foundation, Inc. | Ethanol production using a soy hydrolysate-based medium or a yeast autolysate-based medium |
FI106955B (fi) * | 1998-10-16 | 2001-05-15 | Fortum Oil & Gas Oy | Menetelmä iso-oktaanin valmistamiseksi isobuteenipitoisesta hiilivetysyötöstä |
RU2145354C1 (ru) | 1998-11-24 | 2000-02-10 | Оренбургский государственный университет | Способ подготовки зернового крахмалсодержащего сырья для спиртового брожения |
US6740508B2 (en) * | 1999-02-11 | 2004-05-25 | Renessen Llc | Fermentation-based products from corn and method |
PL207932B1 (pl) * | 1999-03-11 | 2011-02-28 | Zeachem Inc | Sposób wytwarzania etanolu |
WO2001018154A1 (en) * | 1999-09-06 | 2001-03-15 | Agrofuel Ab | Motor fuel for diesel engines |
JP2002345395A (ja) * | 2001-05-30 | 2002-12-03 | Kumiko Ibaraki | シュー生地用配合組成物 |
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