BR112014024524A2 - tetramerização de etileno - Google Patents

tetramerização de etileno

Info

Publication number
BR112014024524A2
BR112014024524A2 BR112014024524A BR112014024524A BR112014024524A2 BR 112014024524 A2 BR112014024524 A2 BR 112014024524A2 BR 112014024524 A BR112014024524 A BR 112014024524A BR 112014024524 A BR112014024524 A BR 112014024524A BR 112014024524 A2 BR112014024524 A2 BR 112014024524A2
Authority
BR
Brazil
Prior art keywords
catalyst
tetramerization
group
ethylene
binding compound
Prior art date
Application number
BR112014024524A
Other languages
English (en)
Other versions
BR112014024524B1 (pt
Inventor
Maumela Hulisani
James Overett Matthew
Stephen Mokhadinyana Molise
Mokgolela Mogorosi Moses
Christopher Maumela Munaka
Original Assignee
Sasol Tech Pty Ltd
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 Sasol Tech Pty Ltd filed Critical Sasol Tech Pty Ltd
Publication of BR112014024524A2 publication Critical patent/BR112014024524A2/pt
Publication of BR112014024524B1 publication Critical patent/BR112014024524B1/pt

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Classifications

    • 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
    • C07C2/36Catalytic processes with hydrides or organic compounds as phosphines, arsines, stilbines or bismuthines
    • 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
    • B01J31/1845Catalysts 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 phosphorus
    • B01J31/1875Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
    • B01J31/188Amide derivatives thereof
    • 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
    • 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
    • C07C2531/24Phosphines
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

resumo patente de invenção: "tetramerização de etileno". a presente invenção refere-se a um processo para a tetramerização de etileno sob condições em fase de solução. é realizada na presença de um catalisador ativado em uma temperatura acima de 80°c e até uma temperatura de cerca de 130°c. o catalisador ativado é fornecido por meio da combinação de uma fonte de cromo e um composto de ligação, cujo composto de ligação inclui pelo menos um grupo de hidrocarbila substituído por flúor, grupo de organoeterila, ou grupo de hetero-hidrocarbila, e opcionalmente um ativador de catalisador ou combinação de ativadores de catalisadores.
BR112014024524A 2012-05-09 2013-05-08 tetramerização de etileno BR112014024524B1 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261644676P 2012-05-09 2012-05-09
PCT/IB2013/053699 WO2013168106A1 (en) 2012-05-09 2013-05-08 Tetramerisation of ethylene

Publications (2)

Publication Number Publication Date
BR112014024524A2 true BR112014024524A2 (pt) 2017-07-25
BR112014024524B1 BR112014024524B1 (pt) 2020-04-22

Family

ID=48699875

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112014024524A BR112014024524B1 (pt) 2012-05-09 2013-05-08 tetramerização de etileno

Country Status (12)

Country Link
US (1) US9487456B2 (pt)
EP (1) EP2847150B1 (pt)
KR (1) KR102138685B1 (pt)
CN (1) CN104220402B (pt)
BR (1) BR112014024524B1 (pt)
CA (1) CA2866773A1 (pt)
ES (1) ES2750659T3 (pt)
IN (1) IN2014DN10416A (pt)
MY (1) MY170070A (pt)
SG (1) SG11201407142WA (pt)
WO (1) WO2013168106A1 (pt)
ZA (1) ZA201406073B (pt)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9499456B2 (en) * 2012-05-09 2016-11-22 Sasol Technology (Proprietary) Limited Tetramerisation of ethylene
KR101657259B1 (ko) * 2013-11-19 2016-09-13 주식회사 엘지화학 리간드 화합물, 올레핀 올리고머화용 촉매계, 및 이를 이용한 올레핀 올리고머화 방법
EP3170805B1 (de) * 2015-11-19 2018-09-12 Evonik Degussa GmbH Beeinflussung der viskosität von auf n-buten basierenden estergemischen durch gezielten einsatz von ethen bei der herstellung der ester-vorprodukte
US9707549B1 (en) 2016-05-26 2017-07-18 Chevron Phillips Chemical Company Lp Ethylene oligomerization catalyst systems using chemically-treated solid oxides
US10414699B2 (en) 2016-05-27 2019-09-17 Chevron Phillips Chemical Company Lp Process improvements in selective ethylene oligomerizations
US10414698B2 (en) 2016-05-27 2019-09-17 Chevron Phillips Chemical Company Lp Reduced polymer formation for selective ethylene oligomerizations
US10329212B2 (en) 2016-05-27 2019-06-25 Chevron Phillips Chemical Company Lp Reduced polymer formation for selective ethylene oligomerizations
FR3051683B1 (fr) 2016-05-31 2020-10-09 Ifp Energies Now Composition catalytique a base de chrome et d'un ligand a base de phosphine et son utilisation dans un procede de procuction d'octenes
KR102018279B1 (ko) 2017-03-23 2019-09-04 에스케이이노베이션 주식회사 파울링 방지제 및 이를 이용한 올레핀의 올리고머화 방법
US10232339B2 (en) 2017-06-06 2019-03-19 Chevron Phillips Chemical Company Lp Fouling protection for an oligomerization reactor inlet
US10493442B2 (en) 2017-09-22 2019-12-03 Chevron Phillips Chemical Company Lp Fluorinated N2-phosphinyl amidine compounds, chromium salt complexes, catalyst systems, and their use to oligomerize ethylene
US10183960B1 (en) 2017-09-22 2019-01-22 Chevron Phillips Chemical Company Lp Perfluorohydrocarbyl-N2-phosphinyl amidine compounds, chromium salt complexes, catalyst systems, and their use to oligomerize ethylene
US10294171B2 (en) 2017-09-22 2019-05-21 Chevron Phillips Chemical Company Lp Carbonyl-containing perfluorohydrocarbyl-N2-phosphinyl amidine compounds, chromium salt complexes and their use to oligomerize ethylene
US10464862B2 (en) 2017-09-28 2019-11-05 Chevron Phillips Chemical Company Lp Oligomerization reactions using aluminoxanes
KR102605188B1 (ko) 2018-02-27 2023-11-24 에스케이이노베이션 주식회사 리간드, 이를 포함하는 올리고머화 촉매 및 이를 이용한 에틸렌 올리고머의 제조방법
WO2020185426A1 (en) 2019-03-13 2020-09-17 Tpc Group Llc Flexible manufacturing system for selectively producing different linear alpha olefins
CN114054095B (zh) * 2020-08-10 2023-11-10 中国石油化工股份有限公司 一种乙烯齐聚催化剂组合物及其应用
CN112473741B (zh) * 2020-10-22 2023-09-01 杭州小菱科技有限公司 一种乙烯齐聚催化剂体系及其制备方法与用途
WO2022115751A1 (en) 2020-11-30 2022-06-02 Saudi Arabian Oil Company Catalyst systems
US11612883B2 (en) 2020-11-30 2023-03-28 Saudi Arabian Oil Company Catalyst systems
US11623208B2 (en) 2020-11-30 2023-04-11 Saudi Arabian Oil Company Catalyst systems
US11440857B2 (en) 2020-11-30 2022-09-13 Saudi Arabian Oil Company Catalyst systems
WO2022115754A1 (en) 2020-11-30 2022-06-02 Saudi Arabian Oil Company Catalyst systems
WO2022191882A1 (en) * 2021-03-12 2022-09-15 Saudi Arabian Oil Company Catalyst systems
WO2023027749A1 (en) 2021-08-26 2023-03-02 Saudi Arabian Oil Company Catalyst systems
CN113731505B (zh) * 2021-09-13 2024-05-03 万华化学集团股份有限公司 一种乙烯齐聚催化剂体系与应用
US11492305B1 (en) 2021-11-08 2022-11-08 Chevron Phillips Chemical Company, Lp Chromium phosphinyl hydroisoindole amidine complexes for tetramerization of ethylene
US11505513B1 (en) 2021-11-08 2022-11-22 Chevron Phillips Chemical Company, Lp Chromium bicyclic phosphinyl amidine complexes for tetramerization of ethylene
US11583843B1 (en) 2021-11-08 2023-02-21 Chevron Phillips Chemical Company, Lp Chromium phosphinyl isoindole amidine complexes for tetramerization of ethylene
US11639321B1 (en) 2022-08-31 2023-05-02 Saudi Arabian Oil Company Catalyst systems that include meta-alkoxy substituted n-aryl bis-diphosphinoamine ligands
US11623901B1 (en) 2022-08-31 2023-04-11 Saudi Arabian Oil Company Catalyst systems that include silyl ether moieties
US12037301B1 (en) 2022-12-20 2024-07-16 King Fahd University Of Petroleum And Minerals Chromium-catalyzed ethylene oligomerization with bulky functionalized N-aryl bisphosphineamine ligands

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG112883A1 (en) 1992-09-17 2005-07-28 Mitsubishi Chem Corp Method for oligomerizing an alpha-olefin
TW354300B (en) 1993-02-17 1999-03-11 Mitsubishi Chem Corp Process for producing <alpha>-olefin oligomers
MY115177A (en) 1994-06-21 2003-04-30 Mitsubishi Chem Corp Process for producing (alpha) -olefin oligomers
US5856257A (en) 1997-05-16 1999-01-05 Phillips Petroleum Company Olefin production
JP2006511694A (ja) 2002-12-20 2006-04-06 サソル テクノロジー (ピーティーワイ) リミテッド オレフィンのタンデム四量体化−重合
BRPI0317510B1 (pt) * 2002-12-20 2020-01-07 Sasol Technology ( Pty) Ltd Processo de tetramerização de olefinas e sistema catalisador
US7414006B2 (en) 2005-03-09 2008-08-19 Exxonmobil Chemical Patents Inc. Methods for oligomerizing olefins
US7323611B2 (en) 2005-06-28 2008-01-29 Sumitomo Chemical Company Limited Process for producing olefin oligomer
WO2007007272A2 (en) 2005-07-12 2007-01-18 Sasol Technology (Pty) Limited Oligomerisation of olefinic compounds in the presence of a diluted metal containing activator
GB0520085D0 (en) 2005-10-03 2005-11-09 Sasol Tech Pty Ltd Oligomerisation of olefinic compounds in the presence of an oligomerisation catalyst, and a catalyst activator including a halogenated -AR group
CA2637703A1 (en) 2006-02-03 2007-08-09 Ineos Europe Limited Transition metal catalysts
US7378537B2 (en) 2006-07-25 2008-05-27 Chevron Phillips Chemical Company Lp Olefin oligomerization catalysts and methods of using same
KR101074202B1 (ko) 2007-01-18 2011-10-14 에스케이종합화학 주식회사 에틸렌 사량체화 촉매계 및 이를 이용한 1-옥텐의 제조방법
CA2583007C (en) 2007-03-29 2015-03-31 Nova Chemicals Corporation Amino phosphine
CA2687259C (en) 2007-05-28 2014-04-15 Sasol Technology (Pty) Limited Two stage activation of oligomerisation catalyst and oligomerisation of olefinic compounds in the presence of an oligomerisation catalyst so activated
US8637721B2 (en) 2007-07-11 2014-01-28 Saudi Basic Industries Corporation Catalyst composition and process for di-, tri- and/or tetramerization of ethylene
KR101057576B1 (ko) 2007-08-16 2011-08-17 에스케이종합화학 주식회사 선택적 에틸렌 올리머고화 촉매계
KR100942978B1 (ko) 2008-07-10 2010-02-17 주식회사 하이닉스반도체 반도체 메모리 소자
CA2639882C (en) 2008-09-29 2016-07-12 Nova Chemicals Corporation Tetramerization
WO2010092554A1 (en) 2009-02-16 2010-08-19 Sasol Technology (Pty) Limited Oligomerisation of olefinic compounds in the presence of an activated oligomerisation catalyst
KR101809226B1 (ko) 2009-10-16 2017-12-14 사솔 테크날러지 (프로프라이어터리) 리미티드 에틸렌을 포함하는 다성분 탄화수소 스트림으로부터 성분들의 분리
MY149647A (en) 2009-10-19 2013-09-30 Sasol Tech Pty Ltd Oligomerisation of olefinic compounds with reduced polymer formation
CA2701252C (en) * 2010-04-20 2017-01-03 Nova Chemicals Corporation Polymer mitigation
CA2703435C (en) * 2010-05-12 2017-05-02 Nova Chemicals Corporation Oligomerization process using a chromium p-n-p catalyst with added alkyl zinc
CA2716714C (en) 2010-10-06 2017-05-16 Nova Chemicals Corporation Tetramerization ligands
US9499456B2 (en) * 2012-05-09 2016-11-22 Sasol Technology (Proprietary) Limited Tetramerisation of ethylene

Also Published As

Publication number Publication date
ES2750659T3 (es) 2020-03-26
IN2014DN10416A (pt) 2015-08-14
CN104220402A (zh) 2014-12-17
EP2847150A1 (en) 2015-03-18
WO2013168106A1 (en) 2013-11-14
ZA201406073B (en) 2015-11-25
BR112014024524B1 (pt) 2020-04-22
US20150087873A1 (en) 2015-03-26
EP2847150B1 (en) 2019-07-17
KR20150016959A (ko) 2015-02-13
SG11201407142WA (en) 2014-11-27
CN104220402B (zh) 2017-02-22
CA2866773A1 (en) 2013-11-14
KR102138685B1 (ko) 2020-07-29
MY170070A (en) 2019-07-03
US9487456B2 (en) 2016-11-08

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B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]

Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 08/05/2013, OBSERVADAS AS CONDICOES LEGAIS.