DK1883616T3 - Fremgangsmåde til kontinuert carbonylering ved supported-ionic-liquid-phase katalyse - Google Patents

Fremgangsmåde til kontinuert carbonylering ved supported-ionic-liquid-phase katalyse

Info

Publication number
DK1883616T3
DK1883616T3 DK06722952T DK06722952T DK1883616T3 DK 1883616 T3 DK1883616 T3 DK 1883616T3 DK 06722952 T DK06722952 T DK 06722952T DK 06722952 T DK06722952 T DK 06722952T DK 1883616 T3 DK1883616 T3 DK 1883616T3
Authority
DK
Denmark
Prior art keywords
catalyst
supported
ionic
liquid
continuous carbonylation
Prior art date
Application number
DK06722952T
Other languages
English (en)
Inventor
Rasmus Fehrmann
Anders Riisager
Original Assignee
Wacker Chemie Ag
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 Wacker Chemie Ag filed Critical Wacker Chemie Ag
Application granted granted Critical
Publication of DK1883616T3 publication Critical patent/DK1883616T3/da

Links

Classifications

    • 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
    • B01J12/00—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor
    • B01J12/007—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor in the presence of catalytically active bodies, e.g. porous plates
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277—Catalysts 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
    • B01J31/0292—Catalysts 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 immobilised on a substrate
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C07C51/12—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide on an oxygen-containing group in organic compounds, e.g. alcohols
    • 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
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00002—Chemical plants
    • B01J2219/00027—Process aspects
    • B01J2219/00033—Continuous processes
    • 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
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00002—Chemical plants
    • B01J2219/00042—Features relating to reactants and process fluids
    • B01J2219/00047—Ionic liquids
    • 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
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32—Addition reactions to C=C or C-C triple bonds
    • B01J2231/321—Hydroformylation, metalformylation, carbonylation or hydroaminomethylation
    • 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
    • B01J2531/822—Rhodium
    • 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
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0277—Catalysts 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
    • B01J31/0278—Catalysts 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
    • B01J31/0281—Catalysts 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
    • B01J31/0284—Catalysts 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
DK06722952T 2005-05-20 2006-05-19 Fremgangsmåde til kontinuert carbonylering ved supported-ionic-liquid-phase katalyse DK1883616T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US68284605P 2005-05-20 2005-05-20
DKPA200500735 2005-05-20
PCT/DK2006/000275 WO2006122563A1 (en) 2005-05-20 2006-05-19 A process for continuous carbonylation by supported ionic liquid-phase catalysis

Publications (1)

Publication Number Publication Date
DK1883616T3 true DK1883616T3 (da) 2009-12-14

Family

ID=36615614

Family Applications (1)

Application Number Title Priority Date Filing Date
DK06722952T DK1883616T3 (da) 2005-05-20 2006-05-19 Fremgangsmåde til kontinuert carbonylering ved supported-ionic-liquid-phase katalyse

Country Status (17)

Country Link
US (1) US8003822B2 (da)
EP (1) EP1883616B1 (da)
JP (1) JP5193028B2 (da)
KR (1) KR101237682B1 (da)
AT (1) ATE444273T1 (da)
AU (1) AU2006246838B2 (da)
BR (1) BRPI0610858A2 (da)
CA (1) CA2608909C (da)
DE (1) DE602006009503D1 (da)
DK (1) DK1883616T3 (da)
EA (1) EA013125B1 (da)
ES (1) ES2332816T3 (da)
MX (1) MX2007014467A (da)
NO (1) NO20076493L (da)
NZ (1) NZ564148A (da)
PT (1) PT1883616E (da)
WO (1) WO2006122563A1 (da)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008132962A1 (ja) * 2007-04-20 2008-11-06 Niigata University オレフィンメタセシス触媒及びそれを用いたメタセシス反応によるオレフィン反応生成物の製造方法
JP5463140B2 (ja) * 2007-06-12 2014-04-09 日宝化学株式会社 イオン液体の製造方法
JP2009214094A (ja) * 2008-02-15 2009-09-24 Tokyo Institute Of Technology 酸化触媒、酸化方法、酸化装置および抗菌剤
DE102009011815A1 (de) 2009-03-05 2010-09-09 Marco Haumann Hybridmaterialien zur heterogen katalysierten asymmetrischen Hydrierung im Gaskontakt und Verfahren zur ihrer Anwendung
DE102009017498A1 (de) * 2009-04-16 2010-10-28 Süd-Chemie AG Verwendung einer Katalysatorzusammensetzung zur Olefinmetathese in der Gasphase und Verfahren zur Olefinmetathese in der Gasphase
DE102009038690B4 (de) * 2009-08-24 2016-04-07 Clariant Produkte (Deutschland) Gmbh Katalysatorzusammensetzung für die Umsetzung von Kohlenmonoxid in Gasströmen
IN2012DN02308A (da) 2009-09-03 2015-08-21 Univ Denmark Tech Dtu
DE102009029284A1 (de) * 2009-09-08 2011-03-10 Evonik Oxeno Gmbh Verfahren zur Oligomerisierung von Olefinen
DE102009051462B4 (de) 2009-10-30 2015-02-05 Clariant International Ag Verfahren zur Herstellung eines Kompositmaterials, Kompositmaterial und dessen Verwendung
US8471086B2 (en) * 2010-06-28 2013-06-25 Chevron U.S.A. Inc. Process to control product selectivity
US8388903B2 (en) * 2010-06-28 2013-03-05 Chevron U.S.A. Inc. Supported ionic liquid reactor
DE102010041821A1 (de) * 2010-09-30 2012-04-05 Evonik Oxeno Gmbh Einsatz von Supported Ionic Liquid Phase (SILP) Katalysatorsystemen in der Hydroformylierung von olefinhaltigen Gemischen zu Aldehydgemischen mit hohem Anteil von in 2-Stellung unverzweigten Aldehyden
ES2639068T3 (es) * 2010-10-05 2017-10-25 Basf Se Producción de alcoholes homoalílicos en presencia de catalizadores en fase líquida iónica inmovilizados de forma no covalente, en condiciones de reacción en fase gaseosa
US8975428B2 (en) 2011-06-03 2015-03-10 Emory University Dirhodium catalyst compositions and synthetic processes related thereto
US20130102819A1 (en) 2011-10-19 2013-04-25 Normen Szesni Catalyst composition for selective hydrogenation with improved characteristics
DE102012202622A1 (de) 2012-02-21 2013-08-22 Wacker Chemie Ag Katalysator zur Carbonylierung carbonylierbarer Verbindungen in der Gasphase
DE102012202621A1 (de) 2012-02-21 2013-08-22 Wacker Chemie Ag Verfahren zur Befüllung eines Reaktors mit einem Katalysator
US9387469B2 (en) 2013-12-30 2016-07-12 Eastman Chemical Company Carbonylation catalyst and process using same
JP6569019B1 (ja) 2018-07-02 2019-08-28 株式会社ダイセル 酢酸の製造方法
CN112295599A (zh) * 2020-10-29 2021-02-02 中国科学院过程工程研究所 一种限域多位点离子液体催化剂用于合成环状碳酸酯

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3608835A (en) * 1967-06-30 1971-09-28 Josef Ruzicka Ultradisintegration and agglomeration of minerals such as mica, products therefrom and apparatus therefor
US3769329A (en) * 1970-03-12 1973-10-30 Monsanto Co Production of carboxylic acids and esters
US4362821A (en) * 1981-10-29 1982-12-07 Texaco Inc. Process for preparing alkanols from synthesis gas
US5001259A (en) * 1984-05-03 1991-03-19 Hoechst Celanese Corporation Methanol carbonylation process
CN1323286A (zh) * 1998-09-10 2001-11-21 埃克森化学专利公司 用离子液制备芳香醛的方法
GB9917429D0 (en) 1999-07-23 1999-09-22 Swan Thomas & Co Ltd Carbonylation reactions
ATE264141T1 (de) * 1999-11-05 2004-04-15 Johnson Matthey Plc Immobilisierte ionische flüssigkeiten
US6617471B2 (en) * 2001-06-20 2003-09-09 Eastman Chemical Company Method for carbonylation of lower aliphatic alcohols using tin promoted iridium catalyst
ATE452869T1 (de) 2002-05-06 2010-01-15 Eastman Chem Co Kontinuierlicher carbonylierungsprozess
FR2839972B1 (fr) 2002-05-23 2005-08-19 Inst Francais Du Petrole Procede de carbonylation des alcools utilisant un catalyseur a base de rhodium ou d'iridium dans un liquide ionique non-aqueux,avec un recyclage efficace du catalyseur
FR2845084B1 (fr) * 2002-09-26 2009-07-17 Centre Nat Rech Scient Compositions contenant des liquides ioniques et leurs utilisations, notamment en synthese organique

Also Published As

Publication number Publication date
US8003822B2 (en) 2011-08-23
PT1883616E (pt) 2009-11-24
US20090030229A1 (en) 2009-01-29
CA2608909A1 (en) 2006-11-23
ES2332816T3 (es) 2010-02-12
MX2007014467A (es) 2008-03-14
BRPI0610858A2 (pt) 2010-08-03
AU2006246838A1 (en) 2006-11-23
EP1883616B1 (en) 2009-09-30
KR101237682B1 (ko) 2013-02-26
WO2006122563A1 (en) 2006-11-23
EA200702547A1 (ru) 2008-04-28
ATE444273T1 (de) 2009-10-15
EA013125B1 (ru) 2010-02-26
KR20080036955A (ko) 2008-04-29
AU2006246838B2 (en) 2010-12-02
DE602006009503D1 (de) 2009-11-12
JP5193028B2 (ja) 2013-05-08
JP2008540107A (ja) 2008-11-20
EP1883616A1 (en) 2008-02-06
NZ564148A (en) 2010-01-29
CA2608909C (en) 2013-08-13
NO20076493L (no) 2007-12-18

Similar Documents

Publication Publication Date Title
NO20076493L (no) En fremgangsmate for kontinuerlig karbonylering med baret ionisk vaeskefasekatalyse
Kar et al. Manganese-catalyzed sequential hydrogenation of CO2 to methanol via formamide
Piccirilli et al. Versatile CO2 hydrogenation–dehydrogenation catalysis with a Ru–PNP/ionic liquid system
Kar et al. Integrative CO2 capture and hydrogenation to methanol with reusable catalyst and amine: toward a carbon neutral methanol economy
ATE452869T1 (de) Kontinuierlicher carbonylierungsprozess
Dang et al. Palladium nanoparticles supported on ZIF-8 as an efficient heterogeneous catalyst for aminocarbonylation
EP1726577A4 (en) METHOD FOR CATALYTIC IMPLEMENTATION USING A MICROREACTOR
ATE306320T1 (de) Zinn aktivierter platinum katalysator für die karbonylierung von niedrigen aliphatischen alkoholen
ATE323063T1 (de) Verfahren zur herstellung von c10-c30-alkenen durch partielle hydrierung von alkinen an festbett-palladium-trägerkatalysatoren
Lv et al. Computational evidence for Lewis base-promoted CO2 hydrogenation to formic acid on gold surfaces
AR083305A2 (es) Catalizador, proceso para prepararlo, proceso para la oxidacion de un sustrato organico y proceso para preparar una sal de acido carboxilico
Nielsen et al. Utilizing glycerol as an ex situ CO-source in Pd-catalyzed alkoxycarbonylation of styrenes
Li et al. Ruthenium trichloride as a new catalyst for selective production of dimethoxymethane from liquid methanol with molecular oxygen as sole oxidant
Kumar et al. Solid-supported ruthenium (0): an efficient heterogeneous catalyst for hydration of nitriles to amides under microwave irradiation
Landge et al. Palladium-catalyzed regioselective arylation of unprotected allylamines
MY138453A (en) Process for producing carbonylation products
AR040319A1 (es) Uso de telurio en catalizadores con contenido de metales nobles y con soporte de carbon para reacciones de oxidacion en fase liquida
Lu et al. Manganese (I)-pincer catalyzed α-alkylation of sulfones by alcohols
Ichikawa et al. Chemoselective hydrogenation of halonitroaromatics over platinum on carbon as catalyst in supercritical carbon dioxide
Erdmann et al. Palladium-catalyzed aerobic oxidative coupling of O-xylene in flow: a safe and scalable protocol for cross-dehydrogenative coupling
UA83040C2 (ru) Способ карбонилирования с применением в качестве катализатора металла, координированного полидентатными лигандами
Natsir et al. Highly catalytic performance of La2O3 in the selective transfer hydrogenation of biomass-derived furfural
Blasucci et al. Combining homogeneous catalysis with heterogeneous separation using tunable solvent systems
Virtanen et al. Kinetics of citral hydrogenation by supported ionic liquid catalysts (SILCA) for fine chemicals
Giroux et al. Synthesis of phenylacetic acids under rhodium-catalyzed carbonylation conditions