JP2008533232A - バイオディーゼルの製造 - Google Patents

バイオディーゼルの製造 Download PDF

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JP2008533232A
JP2008533232A JP2008500252A JP2008500252A JP2008533232A JP 2008533232 A JP2008533232 A JP 2008533232A JP 2008500252 A JP2008500252 A JP 2008500252A JP 2008500252 A JP2008500252 A JP 2008500252A JP 2008533232 A JP2008533232 A JP 2008533232A
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JP2008533232A5 (enExample
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マーティン ジョン アール
ケニス リチャード セドン
ナタリア ヴラディミロヴナ プレチコヴァ
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ザ クィーンズ ユニヴァーシティー オブ ベルファスト
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Publication of JP2008533232A5 publication Critical patent/JP2008533232A5/ja
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0278Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
    • B01J31/0279Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the cationic portion being acyclic or nitrogen being a substituent on a ring
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0278Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
    • B01J31/0281Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member
    • B01J31/0282Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member of an aliphatic ring, e.g. morpholinium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0278Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
    • B01J31/0281Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member
    • B01J31/0284Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member of an aromatic ring, e.g. pyridinium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0287Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre
    • B01J31/0288Phosphorus
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/03Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/003Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fatty acids with alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/04Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
    • C11C3/10Ester interchange
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/40Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/49Esterification or transesterification
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/54Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Liquid Carbonaceous Fuels (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Fats And Perfumes (AREA)
JP2008500252A 2005-03-11 2006-02-27 バイオディーゼルの製造 Pending JP2008533232A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0505064.6A GB0505064D0 (en) 2005-03-11 2005-03-11 Production of bio-diesel
PCT/GB2006/000682 WO2006095134A1 (en) 2005-03-11 2006-02-27 Production of bio-diesel

Publications (2)

Publication Number Publication Date
JP2008533232A true JP2008533232A (ja) 2008-08-21
JP2008533232A5 JP2008533232A5 (enExample) 2009-03-12

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JP2008500252A Pending JP2008533232A (ja) 2005-03-11 2006-02-27 バイオディーゼルの製造

Country Status (5)

Country Link
US (1) US20090235574A1 (enExample)
EP (1) EP1866086A1 (enExample)
JP (1) JP2008533232A (enExample)
GB (1) GB0505064D0 (enExample)
WO (1) WO2006095134A1 (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013183137A1 (ja) * 2012-06-07 2013-12-12 株式会社日立製作所 燃料合成方法及び燃料合成装置
JP2024522789A (ja) * 2021-06-18 2024-06-21 フラオンホファー-ゲゼルシャフト・ツア・フェルデルング・デア・アンゲヴァンテン・フォルシュング・エー・ファオ 硫酸化多糖を調製するための方法、および硫酸化多糖

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100746996B1 (ko) 2006-09-06 2007-08-08 인하대학교 산학협력단 이온성 액체를 이용한 바이오디젤 및 글리세롤의 생산 방법
US8044120B2 (en) * 2006-10-13 2011-10-25 Basf Aktiengesellschaft Ionic liquids for solubilizing polymers
US8598378B2 (en) 2008-03-14 2013-12-03 University Of Hawaii Methods and compositions for extraction and transesterification of biomass components
KR101115283B1 (ko) 2009-10-15 2012-03-13 대상 주식회사 오메가-3 불포화 지방산과 아스코르빈산과의 복합체의 제조방법
KR101125638B1 (ko) * 2010-01-13 2012-03-27 에이치플러스에코 주식회사 중유 에멀젼용 분산 유화제 및 이를 포함하는 중유 에멀젼 연료유
EP2433970A1 (en) 2010-09-28 2012-03-28 Cargill, Incorporated Microprocessing for preparing a polycondensate
US8580886B2 (en) 2011-09-20 2013-11-12 Dow Corning Corporation Method for the preparation and use of bis (alkoxysilylorgano)-dicarboxylates
WO2013081820A2 (en) 2011-12-02 2013-06-06 Dow Corning Corporation Ester-functional silanes and the preparation and use thereof;and use of iminium compounds as phase transfer catalysts
CN102872911B (zh) * 2012-10-23 2015-04-08 吴峰 一种脂肪酸制备方法
CN103074389A (zh) * 2013-02-04 2013-05-01 东莞市合能微生物能源有限公司 一种利用生物酶制备生物柴油的方法
US9435779B2 (en) * 2014-05-05 2016-09-06 Uop Llc Method for quantitation of acid sites in acidic ionic liquids using silane and borane compounds
US9435688B2 (en) * 2014-05-05 2016-09-06 Uop Llc Method for quantitation of acid sites in acidic catalysts using silane and borane compounds
US10233141B2 (en) * 2014-06-13 2019-03-19 Southern Biofuel Technology Pty Ltd Process for the preparation of fatty acid alkyl esters
FR3038853B1 (fr) * 2015-07-16 2019-06-07 Universite De Bourgogne Utilisation de liquides ioniques recyclables comme catalyseurs d'esterification
CN106433994B (zh) * 2016-08-23 2021-04-02 河北工程大学 一种聚合离子液体催化制备生物柴油的方法

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11181451A (ja) * 1997-12-24 1999-07-06 Jatco Corp エステル燃料製造方法及びその装置
JP2000204392A (ja) * 1999-01-13 2000-07-25 Asahi Chem Ind Co Ltd エステル組成物及び製造方法
JP2001247572A (ja) * 2000-03-06 2001-09-11 Central Glass Co Ltd ピリミジン誘導体塩
JP2001247508A (ja) * 2000-03-06 2001-09-11 Central Glass Co Ltd オレフィン化合物の製造方法
JP2002275118A (ja) * 2001-03-15 2002-09-25 Central Glass Co Ltd アルドール反応生成物の製造方法
WO2003022812A1 (de) * 2001-09-12 2003-03-20 Solvent Innovation Gmbh Organische sulfate als ionische flüssigkeiten
WO2003070859A1 (fr) * 2002-02-20 2003-08-28 Revo International Inc. Procede de production d'alkyl ester d'acide gras destine a de l'huile combustible pour diesel
WO2003074494A1 (de) * 2002-03-01 2003-09-12 Solvent Innovation Gmbh Halogenfreie ionische flüssigkeiten
WO2003086605A2 (en) * 2002-04-05 2003-10-23 University Of South Alabama Functionalized ionic liquids, and methods of use thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030163952A1 (en) * 2003-02-19 2003-09-04 Alan Rae Compositions
US20040231234A1 (en) * 2003-05-19 2004-11-25 May Choo Yuen Palm diesel with low pour point for climate countries
CN100497526C (zh) * 2005-07-08 2009-06-10 中国科学院过程工程研究所 基于离子液体的生物柴油合成方法

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11181451A (ja) * 1997-12-24 1999-07-06 Jatco Corp エステル燃料製造方法及びその装置
JP2000204392A (ja) * 1999-01-13 2000-07-25 Asahi Chem Ind Co Ltd エステル組成物及び製造方法
JP2001247572A (ja) * 2000-03-06 2001-09-11 Central Glass Co Ltd ピリミジン誘導体塩
JP2001247508A (ja) * 2000-03-06 2001-09-11 Central Glass Co Ltd オレフィン化合物の製造方法
JP2002275118A (ja) * 2001-03-15 2002-09-25 Central Glass Co Ltd アルドール反応生成物の製造方法
WO2003022812A1 (de) * 2001-09-12 2003-03-20 Solvent Innovation Gmbh Organische sulfate als ionische flüssigkeiten
WO2003070859A1 (fr) * 2002-02-20 2003-08-28 Revo International Inc. Procede de production d'alkyl ester d'acide gras destine a de l'huile combustible pour diesel
WO2003074494A1 (de) * 2002-03-01 2003-09-12 Solvent Innovation Gmbh Halogenfreie ionische flüssigkeiten
WO2003086605A2 (en) * 2002-04-05 2003-10-23 University Of South Alabama Functionalized ionic liquids, and methods of use thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013183137A1 (ja) * 2012-06-07 2013-12-12 株式会社日立製作所 燃料合成方法及び燃料合成装置
JPWO2013183137A1 (ja) * 2012-06-07 2016-01-21 株式会社日立製作所 燃料合成方法及び燃料合成装置
JP2024522789A (ja) * 2021-06-18 2024-06-21 フラオンホファー-ゲゼルシャフト・ツア・フェルデルング・デア・アンゲヴァンテン・フォルシュング・エー・ファオ 硫酸化多糖を調製するための方法、および硫酸化多糖

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US20090235574A1 (en) 2009-09-24
WO2006095134A1 (en) 2006-09-14
GB0505064D0 (en) 2005-04-20
EP1866086A1 (en) 2007-12-19

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