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MXPA03008323A - Metatesis de esteres de acidos grasos insaturados o de acidos grasos insaturados con olefinas inferiores. - Google Patents

Metatesis de esteres de acidos grasos insaturados o de acidos grasos insaturados con olefinas inferiores.

Info

Publication number
MXPA03008323A
MXPA03008323A MXPA03008323A MXPA03008323A MXPA03008323A MX PA03008323 A MXPA03008323 A MX PA03008323A MX PA03008323 A MXPA03008323 A MX PA03008323A MX PA03008323 A MXPA03008323 A MX PA03008323A MX PA03008323 A MXPA03008323 A MX PA03008323A
Authority
MX
Mexico
Prior art keywords
unsaturated fatty
metathesis
acid esters
lower olefins
fatty acid
Prior art date
Application number
MXPA03008323A
Other languages
English (en)
Inventor
Kenneth A Burdett
Original Assignee
Dow Global Technologies Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=23066924&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MXPA03008323(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Dow Global Technologies Inc filed Critical Dow Global Technologies Inc
Publication of MXPA03008323A publication Critical patent/MXPA03008323A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C67/347—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/353—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/165—Polymer immobilised coordination complexes, e.g. organometallic complexes
    • B01J31/1658—Polymer immobilised coordination complexes, e.g. organometallic complexes immobilised by covalent linkages, i.e. pendant complexes with optional linking groups, e.g. on Wang or Merrifield resins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2265—Carbenes or carbynes, i.e.(image)
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2265—Carbenes or carbynes, i.e.(image)
    • B01J31/2269—Heterocyclic carbenes
    • B01J31/2273—Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00—Purification; Separation; Use of additives
    • C07C7/04—Purification; Separation; Use of additives by distillation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00—Purification; Separation; Use of additives
    • C07C7/12—Purification; Separation; Use of additives by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/54—Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543—Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/821—Ruthenium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/825—Osmium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
    • 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
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/10—Process efficiency

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Analytical Chemistry (AREA)
  • Water Supply & Treatment (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
MXPA03008323A 2001-03-26 2002-02-27 Metatesis de esteres de acidos grasos insaturados o de acidos grasos insaturados con olefinas inferiores. MXPA03008323A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US27891401P 2001-03-26 2001-03-26
PCT/US2002/005894 WO2002076920A1 (en) 2001-03-26 2002-02-27 Metathesis of unsaturated fatty acid esters or unsaturated fatty acids with lower olefins

Publications (1)

Publication Number Publication Date
MXPA03008323A true MXPA03008323A (es) 2003-12-11

Family

ID=23066924

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA03008323A MXPA03008323A (es) 2001-03-26 2002-02-27 Metatesis de esteres de acidos grasos insaturados o de acidos grasos insaturados con olefinas inferiores.

Country Status (14)

Country Link
US (2) US7119216B2 (es)
EP (1) EP1377537B1 (es)
JP (1) JP4226906B2 (es)
KR (2) KR100869981B1 (es)
CN (3) CN100509155C (es)
AR (1) AR033202A1 (es)
AU (1) AU2002252124B2 (es)
BR (1) BR0208639A (es)
CA (1) CA2441980C (es)
DE (1) DE60232062D1 (es)
MX (1) MXPA03008323A (es)
PE (1) PE20021029A1 (es)
RU (1) RU2289568C2 (es)
WO (1) WO2002076920A1 (es)

Families Citing this family (93)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2289568C2 (ru) 2001-03-26 2006-12-20 Дау Глобал Текнолоджиз Инк. Способ метатезиса сложных эфиров ненасыщенных жирных кислот или ненасыщенных жирных кислот с низшими олефинами и композиция гетерогенного катализатора, предназначенная для способа метатезиса
JP2005515215A (ja) 2001-12-21 2005-05-26 ローディア インコーポレイティド 成分を懸濁させるための安定な界面活性剤組成物
US7348290B2 (en) 2002-03-11 2008-03-25 Japan Science And Technology Agency Arene-ruthenium complexes immobilized on polymers, catalysts consisting of the complexes, and processes for organic syntheses with the same
BR0309359B1 (pt) 2002-04-29 2014-03-18 Dow Global Technologies Inc Composição de alfa,ômega-poliéster de poliol, composição de alfa,ômega-poliéster poliamina e composição de poliéster poliolefina
CA2512815A1 (en) * 2003-01-13 2004-07-29 Cargill, Incorporated Method for making industrial chemicals
CA2541263A1 (en) * 2003-10-09 2005-05-06 Dow Global Technologies Inc. An improved process for the synthesis of unsaturated alcohols
DE102004033312A1 (de) * 2004-07-08 2006-01-26 Boehringer Ingelheim Pharma Gmbh & Co. Kg Kontinuierliches Metatheseverfahren mit Ruthenium-Katalysatoren
WO2006028809A2 (en) 2004-09-02 2006-03-16 Eastman Chemical Company Optimized production of aromatic dicarboxylic acids
FR2878246B1 (fr) * 2004-11-23 2007-03-30 Inst Francais Du Petrole Procede de co-production d'olefines et d'esters par ethenolyse de corps gras insatures dans des liquides ioniques non-aqueux
AU2006205023C1 (en) 2005-01-10 2012-05-24 Elevance Renewable Sciences, Inc. Candle and candle wax containing metathesis and metathesis-like products
CA2610571C (en) * 2005-06-06 2014-01-28 Dow Global Technologies Inc. Metathesis process for preparing an .alpha.,.omega.-functionalized olefin
CA2613687A1 (en) 2005-07-01 2007-01-11 Orica Australia Pty Ltd Crosslinking method
WO2007081987A2 (en) 2006-01-10 2007-07-19 Elevance Renewable Sciences, Inc. Method of making hydrogenated metathesis products
FR2896498B1 (fr) * 2006-01-24 2008-08-29 Inst Francais Du Petrole Procede de co-production d'olefines et de diesters ou de diacides a partir de corps gras insatures.
US7951232B2 (en) * 2006-02-09 2011-05-31 Elevance Renewable Sciences, Inc. Surface coating compositions and methods
EP2007199A2 (en) * 2006-02-09 2008-12-31 Elevance Renewable Sciences, Inc. Antimicrobial compositions, methods and systems
PL220777B1 (pl) * 2006-03-07 2016-01-29 Elevance Renewable Sciences Kompozycja typu wazeliny i jej zastosowanie oraz emulsja zawierająca zdyspergowaną fazę i jej zastosowanie
WO2007103460A2 (en) * 2006-03-07 2007-09-13 Elevance Renewable Sciences, Inc. Colorant compositions comprising metathesized unsaturated polyol esters
JP5361715B2 (ja) 2006-07-12 2013-12-04 エレバンス リニューアブル サイエンシーズ， インク． 環状オレフィンと種子油および類似物との開環交差メタセシス反応
WO2008008420A1 (en) 2006-07-12 2008-01-17 Elevance Renewable Sciences, Inc. Hot melt adhesive compositions comprising metathesized unsaturated polyol ester wax
US8067610B2 (en) 2006-07-13 2011-11-29 Yann Schrodi Synthesis of terminal alkenes from internal alkenes and ethylene via olefin metathesis
RU2311231C1 (ru) * 2006-08-15 2007-11-27 ООО "Объединенный центр исследований и разработок" Катализатор для получения эфиров акриловой кислоты по реакции метатезиса диалкилмалеатов (варианты) и каталитическая композиция на его основе
DE102006040569A1 (de) * 2006-08-30 2008-03-06 Lanxess Deutschland Gmbh Verfahren zum Metathese-Abbau von Nitrilkautschuken
US8501973B2 (en) * 2006-10-13 2013-08-06 Elevance Renewable Sciences, Inc. Synthesis of terminal alkenes from internal alkenes via olefin metathesis
WO2008140468A2 (en) * 2006-10-13 2008-11-20 Elevance Renewable Sciences, Inc. METHODS OF MAKING α, ω -DICARBOXYLIC ACID ALKENE DERIVATIVES BY METATHESIS
WO2008063322A2 (en) * 2006-10-13 2008-05-29 Elevance Renewable Sciences, Inc. Metathesis methods involving hydrogenation and compositions relating to same
WO2008048522A1 (en) * 2006-10-13 2008-04-24 Elevance Renewable Sciences, Inc. Methods of making monounsaturated functionalized alkene compounds by metathesis
WO2008048520A2 (en) 2006-10-13 2008-04-24 Elevance Renewable Sciences, Inc. Methods of making organic compounds by metathesis and hydrocyanation
RU2326733C1 (ru) * 2007-03-29 2008-06-20 ООО "Объединенный центр исследований и разработок" Каталитическая композиция для получения эфиров акриловой кислоты по реакции метатезиса диалкилмалеатов с этиленом
US7691258B2 (en) * 2007-06-04 2010-04-06 Emirates National Oil Company Limited (Enoc) Llc Process for treating hydrocarbon liquid compositions
WO2009003085A1 (en) * 2007-06-27 2008-12-31 Arkema Inc. Process for the manufacture of hydrofluoroolefins via metathesis
EP2183205A4 (en) 2007-08-09 2013-10-02 Elevance Renewable Sciences CHEMICAL PROCESSES FOR TREATING METATHESIS RAW MATERIAL
FR2921362B1 (fr) * 2007-09-20 2012-09-21 Arkema France Procede de synthese d'acides gras omega-insatures
US20090203950A1 (en) * 2008-02-12 2009-08-13 Halsey Richard B Metathesis process using a fluidized bed reactor
WO2010051268A1 (en) 2008-10-31 2010-05-06 Dow Global Technologies Inc. Olefin metathesis process employing bimetallic ruthenium complex with bridging hydrido ligands
KR101654955B1 (ko) 2008-11-26 2016-09-06 엘레반스 리뉴어블 사이언시즈, 인코포레이티드 복분해 반응을 통하여 천연유 공급원료로부터 제트 연료를 제조하는 방법
WO2010062932A1 (en) 2008-11-26 2010-06-03 Elevance Renewable Sciences, Inc. Methods of producing jet fuel from natural oil feedstocks through oxygen-cleaved reactions
US8071799B2 (en) 2009-01-29 2011-12-06 Energy & Environmental Research Center Foundation Chain-selective synthesis of fuel components and chemical feedstocks
US9000246B2 (en) 2009-10-12 2015-04-07 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US9222056B2 (en) 2009-10-12 2015-12-29 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US9175231B2 (en) 2009-10-12 2015-11-03 Elevance Renewable Sciences, Inc. Methods of refining natural oils and methods of producing fuel compositions
US9382502B2 (en) 2009-10-12 2016-07-05 Elevance Renewable Sciences, Inc. Methods of refining and producing isomerized fatty acid esters and fatty acids from natural oil feedstocks
US9169447B2 (en) 2009-10-12 2015-10-27 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US8735640B2 (en) 2009-10-12 2014-05-27 Elevance Renewable Sciences, Inc. Methods of refining and producing fuel and specialty chemicals from natural oil feedstocks
PL2488474T3 (pl) * 2009-10-12 2017-07-31 Elevance Renewable Sciences, Inc. Sposoby rafinacji i wytwarzania paliw z surowców na bazie olejów naturalnych
US9365487B2 (en) 2009-10-12 2016-06-14 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US9051519B2 (en) 2009-10-12 2015-06-09 Elevance Renewable Sciences, Inc. Diene-selective hydrogenation of metathesis derived olefins and unsaturated esters
US8237003B2 (en) * 2009-11-09 2012-08-07 Exxonmobil Chemical Patents Inc. Metathesis catalyst and process for use thereof
WO2011056881A2 (en) * 2009-11-09 2011-05-12 Exxonmobil Chemical Patents Inc. Metathesis catalyst and process for use thereof
US8809563B2 (en) 2009-11-09 2014-08-19 Exxonmobil Chemical Patents Inc. Metathesis catalyst and process for use thereof
US9024034B2 (en) * 2009-11-09 2015-05-05 Exxonmobil Chemical Patents Inc. Metathesis catalysts and processes for use thereof
US8329921B2 (en) 2009-11-09 2012-12-11 Exxonmobil Chemical Patents Inc. Metathesis catalyst and process for use thereof
WO2011100022A2 (en) 2010-02-12 2011-08-18 Exxonmobil Chemical Patents Inc. Metathesis catalyst and process for use thereof
US9115076B2 (en) 2010-04-26 2015-08-25 The United States Of America, As Represented By The Secretary Of Agriculture Process for preparing saturated branched chain fatty acids
US8748641B2 (en) 2010-05-05 2014-06-10 The United States Of America, As Represented By The Secretary Of Agriculture Process for preparing saturated branched chain fatty acids
WO2011136903A1 (en) * 2010-04-26 2011-11-03 The United States Of America As Represented By The Secretary Of Agriculture Process for preparing saturated branched chain fatty acids
JP5996527B2 (ja) 2010-05-28 2016-09-21 テラヴィア ホールディングス， インコーポレイテッド 用途に応じた油を含む食品成分
CA2809361C (en) 2010-08-31 2018-11-06 Biosynthetic Technologies, Llc Catalytic processes for preparing estolide base oils
US8227371B2 (en) 2010-09-24 2012-07-24 Exxonmobil Chemical Patents Inc. Class of olefin metathesis catalysts, methods of preparation, and processes for the use thereof
AU2012212079B2 (en) 2011-02-02 2016-07-28 Corbion Biotech, Inc. Tailored oils produced from recombinant oleaginous microorganisms
US20120289617A1 (en) * 2011-05-10 2012-11-15 Saudi Arabian Oil Company Hybrid Catalyst for Olefin Metathesis
US9181360B2 (en) 2011-08-12 2015-11-10 Exxonmobil Chemical Patents Inc. Polymers prepared by ring opening / cross metathesis
CA2894831C (en) * 2011-12-19 2020-09-08 Biosynthetic Technologies, Llc Processes for preparing estolide base oils and oligomeric compounds that include cross metathesis
US9139493B2 (en) 2011-12-22 2015-09-22 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9133416B2 (en) 2011-12-22 2015-09-15 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9169174B2 (en) 2011-12-22 2015-10-27 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
CN104508101A (zh) 2011-12-28 2015-04-08 艾勒旺斯可再生科学公司 可再生脂肪酸蜡及其制造方法
GB201204715D0 (en) 2012-03-18 2012-05-02 Croda Int Plc Metathesis of olefins using ruthenium-based catalytic complexes
SG11201406711TA (en) 2012-04-18 2014-11-27 Solazyme Inc Tailored oils
WO2013175894A1 (ja) * 2012-05-21 2013-11-28 日本ゼオン株式会社 架橋環状オレフィン樹脂フィルム、積層体及びそれらの製造方法
WO2013191750A1 (en) 2012-06-18 2013-12-27 Biosynthetic Technologies, Llc Processes of preparing estolide compounds that include removing sulfonate residues
EP2864447B3 (en) 2012-06-20 2019-07-17 Elevance Renewable Sciences, Inc. Natural oil metathesis compositions
PL400162A1 (pl) * 2012-07-27 2014-02-03 Apeiron Synthesis Spólka Z Ograniczona Odpowiedzialnoscia Nowe kompleksy rutenu, ich zastosowanie w reakcjach metatezy oraz sposób prowadzenia reakcji metatezy
AU2013329413B2 (en) * 2012-10-09 2017-11-23 Wilmar Trading Pte Ltd Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US9388098B2 (en) 2012-10-09 2016-07-12 Elevance Renewable Sciences, Inc. Methods of making high-weight esters, acids, and derivatives thereof
WO2014176515A2 (en) 2013-04-26 2014-10-30 Solazyme, Inc. Low polyunsaturated fatty acid oils and uses thereof
MX369685B (es) 2013-10-04 2019-11-19 Terravia Holdings Inc Aceites adaptables.
WO2016134138A1 (en) * 2015-02-20 2016-08-25 Biosynthetic Technologies, Llc Processes for preparing estolide base oils and biobased compounds that include ethyleneolysis
WO2016164495A1 (en) 2015-04-06 2016-10-13 Solazyme, Inc. Oleaginous microalgae having an lpaat ablation
CN105419941B (zh) * 2015-11-18 2017-08-22 天津斯瑞吉高新科技研究院有限公司 从棉籽油来制取高附加值产品的一种有效预处理方法
US10280256B2 (en) * 2016-04-20 2019-05-07 Elevance Renewable Sciences, Inc. Renewably derived polyesters and methods of making and using the same
CN114106057B (zh) 2016-10-19 2023-06-23 优美科股份公司及两合公司 Ru亚烷基络合物的合成与表征
US20180155497A1 (en) * 2016-10-25 2018-06-07 Elevance Renewable Sciences, Inc. Renewably Derived Polyamides and Methods of Making the Same
US11471867B2 (en) * 2017-06-23 2022-10-18 Gwangju Institute Of Science And Technology Ligand for forming ruthenium complex, ruthenium complex catalyst, production method therefor and use thereof
CN109364998B (zh) * 2018-10-15 2021-07-06 天津科技大学 一种用于烯烃复分解反应的催化剂及其制备和应用方法
EP3650436A1 (en) 2018-11-06 2020-05-13 Skotan S.A. Method of preparing a mixture of 9-decenoic acid ethyl and 1-decene in an ethenolysis reaction from a raw material of technical purity
EP4115975A4 (en) * 2020-03-03 2024-05-15 Takasago International Corporation CATALYST CONTAINING ACTIVATED CARBON ON WHICH A RUTHENIUM COMPLEX IS ADSORBED, AND METHOD FOR PRODUCING A REDUCTION PRODUCT USING SAME
DE102020119024A1 (de) 2020-07-17 2022-01-20 Werner & Mertz Gmbh Verfahren zur Herstellung eines biobasierten Produkts, entsprechendes Produkt und Verwendungen
EP4182423A1 (de) 2020-07-17 2023-05-24 Werner & Mertz GmbH Verfahren zur herstellung eines biobasierten produkts, entsprechendes produkt und verwendungen
EP3974499A1 (en) 2020-09-28 2022-03-30 Indian Oil Corporation Limited Production of linear alpha olefins
CN112876360A (zh) * 2021-01-25 2021-06-01 南京工业大学 一种植物油多元醇及其制备方法与应用
EP4292706A4 (en) 2021-02-11 2025-01-22 Petroleo Brasileiro S.A. - PETROBRAS PROCESS FOR THE CO-PRODUCTION OF C10 TO C13 OLEFINS AND ESTERS FROM METHYL FATTY ACID ESTERS
US11858872B2 (en) * 2021-03-30 2024-01-02 ExxonMobil Technology and Engineering Company High yield jet fuel from mixed fatty acids

Family Cites Families (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE281594C (es)
JPS5677243A (en) 1979-11-29 1981-06-25 Takasago Corp Production of 9-octadecenedioic acid diester
EP0328230A3 (en) 1981-11-19 1990-03-21 Fuji Oil Company, Limited Method for the modification of fats and oils
EP0084437A1 (en) 1982-01-13 1983-07-27 BP Chemicals Limited Dismutation of functionalised olefins
CA1219596A (en) 1982-07-20 1987-03-24 Dennis S. Banasiak Disproportionation of functional olefins
US4560792A (en) 1982-07-20 1985-12-24 Phillips Petroleum Company Disproportionation of functional olefins
US4545941A (en) 1983-06-20 1985-10-08 A. E. Staley Manufacturing Company Co-metathesis of triglycerides and ethylene
DE3612539A1 (de) 1986-04-14 1987-10-15 Huels Chemische Werke Ag Verfahren zur herstellung von technisch reinem, chlorfreiem cyclohexadecadien
US4943397A (en) 1988-09-22 1990-07-24 Shell Oil Company Metathesis of functional olefins
US5342985A (en) 1988-12-10 1994-08-30 Hoechst Ag Organic derivatives of rhenium oxides and their preparation and use for the metathesis of olefins
JPH0366725A (ja) 1989-08-04 1991-03-22 Japan Synthetic Rubber Co Ltd 重合体の製造方法
DE4006540A1 (de) 1990-03-02 1991-09-05 Huels Chemische Werke Ag Katalysatoren fuer die metathese von olefinen und funktionalisierten olefinen
DE4006539A1 (de) 1990-03-02 1991-09-05 Huels Chemische Werke Ag Verfahren zur metathese von olefinen und funktionalisierten olefinen
DE59105881D1 (de) 1990-03-28 1995-08-03 Hoechst Ag Verwendung von organischen derivaten von rheniumoxiden als katalysatoren zur äthenolytischen metathese olefinischer verbindungen und verfahren zur äthenolytischen metathese von olefinischen verbindungen mit hilfe dieser katalysatoren.
DE4107056A1 (de) 1991-03-06 1992-09-10 Huels Chemische Werke Ag Rheniumkatalysatoren fuer die metathese von olefinen und funktionalisierten olefinen
EP1251135A3 (en) * 1992-04-03 2004-01-02 California Institute Of Technology High activity ruthenium or osmium metal carbene complexes for olefin metathesis reactions and synthesis thereof
US5312940A (en) 1992-04-03 1994-05-17 California Institute Of Technology Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization
US5352812A (en) 1993-07-08 1994-10-04 E. I. Du Pont De Nemours And Company Metathesis of acyclic olefins using an iridium/silver catalyst composition
US5539060A (en) 1993-07-30 1996-07-23 Nippon Zeon Co., Ltd. Method for hydrogenation of metathesis polymers
US5831108A (en) 1995-08-03 1998-11-03 California Institute Of Technology High metathesis activity ruthenium and osmium metal carbene complexes
US6225426B1 (en) 1996-04-10 2001-05-01 Uniroyal Chemical Company, Inc. Process for producing polyolefin elastomer employing a metallocene catalyst
US6159890A (en) 1996-04-30 2000-12-12 Bp Amoco Corporation Ruthenium-containing catalyst system for olefin metathesis
US6156692A (en) 1996-04-30 2000-12-05 Bp Amoco Corporation Ruthenium-containing catalyst composition for olefin metathesis
DE19654074C2 (de) 1996-12-23 2001-01-25 Bayer Ag Verfahren zur Herstellung hydrierter ringgeöffneter Metathesepolymeren
TW411348B (en) 1997-05-28 2000-11-11 Mitsui Chemicals Inc Preparation of hydrogenated product of cyclic olefin ring-opening metathesis polymer
BR9810488A (pt) * 1997-06-27 2000-09-12 Ciba Sc Holding Ag Novos catalisadores.
DE19815275B4 (de) 1998-04-06 2009-06-25 Evonik Degussa Gmbh Alkylidenkomplexe des Rutheniums mit N-heterozyklischen Carbenliganden und deren Verwendung als hochaktive, selektive Katalysatoren für die Olefin-Metathese
EP1115491B1 (en) 1998-09-10 2009-08-05 University Of New Orleans Foundation Catalyst complex with phenylindenylidene ligand
ATE398133T1 (de) 1999-03-31 2008-07-15 California Inst Of Techn Mit triazolydin-liganden koordinierte rutheniummetall-alkyliden-komplexe die hohe olefin-metathese-aktivität aufweisen
ATE248182T1 (de) 1999-05-24 2003-09-15 California Inst Of Techn Imidazolidin enthaltende metallcarben- katalysatoren für die metathese
DE10041345A1 (de) 2000-08-23 2002-03-07 Basf Ag Verfahren zur Synthese von terminalen Olefinen mit enger Molgewichtsverteilung
RU2289568C2 (ru) 2001-03-26 2006-12-20 Дау Глобал Текнолоджиз Инк. Способ метатезиса сложных эфиров ненасыщенных жирных кислот или ненасыщенных жирных кислот с низшими олефинами и композиция гетерогенного катализатора, предназначенная для способа метатезиса
BR0309359B1 (pt) 2002-04-29 2014-03-18 Dow Global Technologies Inc Composição de alfa,ômega-poliéster de poliol, composição de alfa,ômega-poliéster poliamina e composição de poliéster poliolefina
US7147749B2 (en) 2002-09-30 2006-12-12 Tokyo Electron Limited Method and apparatus for an improved upper electrode plate with deposition shield in a plasma processing system
CA2541263A1 (en) 2003-10-09 2005-05-06 Dow Global Technologies Inc. An improved process for the synthesis of unsaturated alcohols
EP1817097A2 (en) 2004-10-21 2007-08-15 Dow Gloval Technologies Inc. Membrane separation of a metathesis reaction mixture
CA2610571C (en) 2005-06-06 2014-01-28 Dow Global Technologies Inc. Metathesis process for preparing an .alpha.,.omega.-functionalized olefin
US8530579B2 (en) 2006-08-25 2013-09-10 Dow Global Technologies Llc Production of metathesis products by high melting polymer segment interchange
US8048961B2 (en) 2006-08-25 2011-11-01 Dow Global Technologies Llc Production of metathesis products by amorphous polymer segment interchange
US7956132B2 (en) 2006-08-25 2011-06-07 Dow Global Technologies Llc Production of telechelic compounds by metathesis depolymerization
WO2008027283A2 (en) 2006-08-25 2008-03-06 Dow Global Technologies Inc. Production of meta-block copolymers by polymer segment interchange

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BR0208639A (pt) 2004-08-10
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