MX348699B - Método para el aislamiento de productos de la oligomerización de olefina y la descomposición de residuos de catalizador de oligomerización. - Google Patents

Método para el aislamiento de productos de la oligomerización de olefina y la descomposición de residuos de catalizador de oligomerización.

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Publication number
MX348699B
MX348699B MX2013015205A MX2013015205A MX348699B MX 348699 B MX348699 B MX 348699B MX 2013015205 A MX2013015205 A MX 2013015205A MX 2013015205 A MX2013015205 A MX 2013015205A MX 348699 B MX348699 B MX 348699B
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MX
Mexico
Prior art keywords
oligomerization
olefin
products
catalyst
isolation
Prior art date
Application number
MX2013015205A
Other languages
English (en)
Other versions
MX2013015205A (es
Inventor
Timur Mikhailovich Zilbershtein
Maxim Vladimirovich Lipskikh
Vladislav Alexandrovich Kardash
Vladlena Vladimirovna Suvorova
Original Assignee
Sibur Holding Public Joint Stock Co
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Publication date
Application filed by Sibur Holding Public Joint Stock Co filed Critical Sibur Holding Public Joint Stock Co
Publication of MX2013015205A publication Critical patent/MX2013015205A/es
Publication of MX348699B publication Critical patent/MX348699B/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08Catalytic processes
    • C07C2/26Catalytic processes with hydrides or organic compounds
    • C07C2/32Catalytic processes with hydrides or organic compounds as complexes, e.g. acetyl-acetonates
    • C07C2/34Metal-hydrocarbon complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/04Purification; Separation; Use of additives by distillation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/24Chromium, molybdenum or tungsten
    • B01J23/26Chromium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/24Nitrogen compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08Catalytic processes
    • C07C2/26Catalytic processes with hydrides or organic compounds
    • C07C2/32Catalytic processes with hydrides or organic compounds as complexes, e.g. acetyl-acetonates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/148Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
    • C07C7/17Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound with acids or sulfur oxides
    • 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
    • B01J2231/20Olefin oligomerisation or telomerisation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/60Complexes comprising metals of Group VI (VIA or VIB) as the central metal
    • B01J2531/62Chromium
    • 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
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/14Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • B01J31/143Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron of aluminium
    • 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
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • C07C2531/14Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/22Organic complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/26Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24
    • C07C2531/34Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24 of chromium, molybdenum or tungsten
    • 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
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
    • 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
    • Y02P20/584Recycling of catalysts

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Water Supply & Treatment (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

La invención se relaciona con el campo de producción de oligómeros de olefina, los cuales se usan ampliamente como copolímeros, una materia prima para la preparación de aceites y lubricantes, y también una materia prima para producir otros productos químicos; la invención se relaciona con la producción de oligómeros de olefina por medio de un método de oligomerización de olefinas, y, en particular, con un método de aislamiento de productos de oligomerización de olefina y de descomposición de residuos de catalizador de oligomerización; un método para aislar productos de una reacción de oligomerización de olefinas que comprende un doble enlace terminal, en donde la reacción se lleva a cabo por medio de la acción de un catalizador que comprende compuestos de cromo, un ligando que contiene nitrógeno y compuestos de organoaluminio, comprende un paso de aislar productos independientes de olefina y un paso de tratar residuos de catalizador, caracterizado en que el método comprende los siguientes pasos secuenciales: a) aislar al menos un producto líquido de la reacción de oligomerización de olefinas de una corriente de salida de un reactor de oligomerización; b) tratar un residuo con una solución acuosa de un ácido; y c) separar una capa orgánica y una capa acuosa; primero, el uso de los métodos propuestos permite el aislamiento de productos de reacción objetivo, evitando el ingreso de impurezas de sustancias extrañas, como alcoholes en productos y)o solvente recurrente, y la eliminación de la necesidad de la separación de estas sustancias extrañas; en segundo lugar, el uso del método propuesto hace posible evitar la contaminación de tuberías y dispositivos entre el reactor y la columna de destilación con un producto secundario; en tercer lugar, la solución hace posible separar residuos de catalizador de un subproducto de polímero, facilitando así la regeneración del catalizador o la separación de compuestos metálicos de residuos de catalizador, mientras se evita la precipitación de una resma durante la destilación de los productos de reacción de alta ebullición.
MX2013015205A 2011-06-22 2012-06-21 Método para el aislamiento de productos de la oligomerización de olefina y la descomposición de residuos de catalizador de oligomerización. MX348699B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
RU2011125946/04A RU2471762C1 (ru) 2011-06-22 2011-06-22 Способ выделения продуктов олигомеризации олефинов и разложения остатков катализатора олигомеризации
PCT/RU2012/000484 WO2012177183A1 (ru) 2011-06-22 2012-06-21 Способ выделения продуктов олигомеризации олефинов и разложения остатков катализатора олигомеризации

Publications (2)

Publication Number Publication Date
MX2013015205A MX2013015205A (es) 2014-08-18
MX348699B true MX348699B (es) 2017-06-26

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
MX2013015205A MX348699B (es) 2011-06-22 2012-06-21 Método para el aislamiento de productos de la oligomerización de olefina y la descomposición de residuos de catalizador de oligomerización.

Country Status (11)

Country Link
US (1) US9586874B2 (es)
EP (1) EP2725003B1 (es)
JP (1) JP5866005B2 (es)
KR (1) KR101694388B1 (es)
CN (1) CN103649022B (es)
CA (1) CA2839862C (es)
EA (1) EA024179B1 (es)
MX (1) MX348699B (es)
RU (1) RU2471762C1 (es)
WO (1) WO2012177183A1 (es)
ZA (1) ZA201309147B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2017008376A (es) * 2014-12-23 2018-04-11 Sibur Holding Public Joint Stock Co Metodos de preparacion de oligomeros de una olefina.
US10508065B2 (en) * 2014-12-23 2019-12-17 Public Joint Stock Company “SIBUR Holding” Methods of preparing oligomers of an olefin
KR102113798B1 (ko) * 2014-12-23 2020-05-21 퍼블릭 조인트 스톡 컴퍼니 “시부르 홀딩” 올레핀 올리고머화 반응에서 폴리머 및 불활성화된 유기금속 촉매의 침전 방법
EP3245179A1 (en) * 2015-01-16 2017-11-22 SABIC Global Technologies B.V. Method for emulsion removal in amine removal unit
MX2019005549A (es) * 2016-11-14 2019-07-04 Sibur Holding Public Joint Stock Co Sistema catalizador usado en la oligomerizacion de olefinas y metodo para la oligomerizacion de olefinas.
KR102604431B1 (ko) * 2018-07-26 2023-11-22 에스케이이노베이션 주식회사 선형 알파 올레핀 제조방법
KR20220104418A (ko) * 2021-01-18 2022-07-26 주식회사 엘지화학 올리고머 제조방법

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FR2650760B1 (fr) * 1989-08-08 1991-10-31 Inst Francais Du Petrole Nouvelle composition catalytique et sa mise en oeuvre pour l'oligomerisation des monoolefines
DE4338415C1 (de) * 1993-11-10 1995-03-16 Linde Ag Verfahren zur Katalysatordesaktivierung bei der katalytisch beschleunigten Herstellung linearer Alpha-Olefine durch Oligomerisierung von Ethylen
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Also Published As

Publication number Publication date
EP2725003B1 (en) 2016-11-02
US9586874B2 (en) 2017-03-07
EP2725003A1 (en) 2014-04-30
EP2725003A4 (en) 2014-11-26
KR101694388B1 (ko) 2017-01-10
JP2014525900A (ja) 2014-10-02
RU2471762C1 (ru) 2013-01-10
ZA201309147B (en) 2014-08-27
EA024179B1 (ru) 2016-08-31
CN103649022A (zh) 2014-03-19
KR20140047665A (ko) 2014-04-22
JP5866005B2 (ja) 2016-02-17
CA2839862C (en) 2016-11-08
EA201490054A1 (ru) 2014-04-30
WO2012177183A1 (ru) 2012-12-27
CN103649022B (zh) 2015-11-25
MX2013015205A (es) 2014-08-18
CA2839862A1 (en) 2012-12-27
US20140121435A1 (en) 2014-05-01

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