MY170070A - Tetramerisation of ethylene - Google Patents

Tetramerisation of ethylene

Info

Publication number
MY170070A
MY170070A MYPI2014002328A MYPI2014002328A MY170070A MY 170070 A MY170070 A MY 170070A MY PI2014002328 A MYPI2014002328 A MY PI2014002328A MY PI2014002328 A MYPI2014002328 A MY PI2014002328A MY 170070 A MY170070 A MY 170070A
Authority
MY
Malaysia
Prior art keywords
catalyst
tetramerisation
group
ligating compound
ethylene
Prior art date
Application number
MYPI2014002328A
Other languages
English (en)
Inventor
Hulisani Maumela
Matthew James Overett
Munaka Christopher Maumela
Moses Mokgolela Mogorosi
Molise Stephen Mokhadinyana
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 MY170070A publication Critical patent/MY170070A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04—Preparation 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
    • C07C2/06—Preparation 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
    • C07C2/08—Catalytic processes
    • C07C2/26—Catalytic processes with hydrides or organic compounds
    • C07C2/36—Catalytic processes with hydrides or organic compounds as phosphines, arsines, stilbines or bismuthines
    • 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
    • B01J31/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • B01J31/143—Catalysts 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
    • 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
    • B01J31/18—Catalysts 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
    • B01J31/1845—Catalysts 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
    • B01J31/1875—Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
    • B01J31/188—Amide derivatives thereof
    • 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
    • B01J2231/20—Olefin oligomerisation or telomerisation
    • 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
    • B01J2531/60—Complexes comprising metals of Group VI (VIA or VIB) as the central metal
    • B01J2531/62—Chromium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • C07C2531/14—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/24—Phosphines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24
    • C07C2531/34—Catalysts 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
    • 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
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements 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)
MYPI2014002328A 2012-05-09 2013-05-08 Tetramerisation of ethylene MY170070A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201261644676P 2012-05-09 2012-05-09

Publications (1)

Publication Number Publication Date
MY170070A true MY170070A (en) 2019-07-03

Family

ID=48699875

Family Applications (1)

Application Number Title Priority Date Filing Date
MYPI2014002328A MY170070A (en) 2012-05-09 2013-05-08 Tetramerisation of ethylene

Country Status (12)

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

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MY164873A (en) * 2012-05-09 2018-01-30 Sasol Tech Pty Ltd Tetramerisation of ethylene
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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
US10329212B2 (en) 2016-05-27 2019-06-25 Chevron Phillips Chemical Company Lp Reduced polymer formation for selective ethylene oligomerizations
US10414698B2 (en) 2016-05-27 2019-09-17 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
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
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
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
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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
US11458462B2 (en) 2020-11-30 2022-10-04 Saudi Arabian Oil Company Catalyst systems
US11612883B2 (en) 2020-11-30 2023-03-28 Saudi Arabian Oil Company Catalyst systems
WO2022115749A1 (en) * 2020-11-30 2022-06-02 Saudi Arabian Oil Company Catalyst systems
US11458463B2 (en) 2020-11-30 2022-10-04 Saudi Arabian Oil Company Catalyst systems
US11623208B2 (en) 2020-11-30 2023-04-11 Saudi Arabian Oil Company Catalyst systems
US11529622B2 (en) 2021-03-12 2022-12-20 Saudi Arabian Oil Company Catalyst systems
US11484871B1 (en) 2021-08-26 2022-11-01 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
US11505513B1 (en) 2021-11-08 2022-11-22 Chevron Phillips Chemical Company, Lp Chromium bicyclic phosphinyl amidine complexes for tetramerization of ethylene
US11492305B1 (en) 2021-11-08 2022-11-08 Chevron Phillips Chemical Company, Lp Chromium phosphinyl hydroisoindole 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
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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
KR102864902B1 (ko) * 2023-05-19 2025-09-26 한화토탈에너지스 주식회사 고분자 생성 저감 및 생산성이 향상된 에틸렌 올리고머화 방법

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Also Published As

Publication number Publication date
US9487456B2 (en) 2016-11-08
KR20150016959A (ko) 2015-02-13
ES2750659T3 (es) 2020-03-26
KR102138685B1 (ko) 2020-07-29
IN2014DN10416A (enExample) 2015-08-14
BR112014024524A2 (pt) 2017-07-25
WO2013168106A1 (en) 2013-11-14
US20150087873A1 (en) 2015-03-26
CN104220402A (zh) 2014-12-17
EP2847150B1 (en) 2019-07-17
SG11201407142WA (en) 2014-11-27
EP2847150A1 (en) 2015-03-18
CN104220402B (zh) 2017-02-22
CA2866773A1 (en) 2013-11-14
ZA201406073B (en) 2015-11-25
BR112014024524B1 (pt) 2020-04-22

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