ES329470A1 - A procedure for preparing linear alfaolephins. (Machine-translation by Google Translate, not legally binding) - Google Patents

A procedure for preparing linear alfaolephins. (Machine-translation by Google Translate, not legally binding)

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Publication number
ES329470A1
ES329470A1 ES0329470A ES329470A ES329470A1 ES 329470 A1 ES329470 A1 ES 329470A1 ES 0329470 A ES0329470 A ES 0329470A ES 329470 A ES329470 A ES 329470A ES 329470 A1 ES329470 A1 ES 329470A1
Authority
ES
Spain
Prior art keywords
group
compound
translation
machine
legally binding
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
ES0329470A
Other languages
Spanish (es)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
Esso Research and Engineering Co
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 Esso Research and Engineering Co filed Critical Esso Research and Engineering Co
Publication of ES329470A1 publication Critical patent/ES329470A1/en
Expired legal-status Critical Current

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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
    • C07C2/30Catalytic processes with hydrides or organic compounds containing metal-to-carbon bond; Metal hydrides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06Halogens; Compounds thereof
    • C07C2527/135Compounds comprising a halogen and titanum, zirconium, hafnium, germanium, tin or lead
    • 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
    • C07C2531/04Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A process for preparing linear alpha-olefins having an average molecular weight of about 70 to 300, by polymerization of a gas containing ethylene in the presence of a catalyst comprising the reaction product of a transition metal halide selected from the group consists of TiX4, TiX3OR ', TiX3OOCR', where X is selected from the group consisting of chlorine and bromine and R 'is selected from the group consisting of alkyl, aryl, aralkyl, and cycloalkyl; and an aluminum alkyl compound such that the final formula of the aluminum alkyl compound is AlRnX3, where R is selected from the group consisting of alkyl, aralkyl, and cycloalkyl, X is selected from the group consisting of chlorine, bromine, and iodine, and is less than 2, in the presence of a polar diluent at a tempera ture of less than 75º C and a pressure above 3.5 kg/cm2 absolute, characterized by the addition, to the reaction mixture of a caustic compound and if Desires a catalyst-destroying compound selected from the group consisting of water, acids and alcohols. (Machine-translation by Google Translate, not legally binding)
ES0329470A 1966-07-01 1966-07-23 A procedure for preparing linear alfaolephins. (Machine-translation by Google Translate, not legally binding) Expired ES329470A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US56208966A 1966-07-01 1966-07-01

Publications (1)

Publication Number Publication Date
ES329470A1 true ES329470A1 (en) 1967-05-16

Family

ID=24244750

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0329470A Expired ES329470A1 (en) 1966-07-01 1966-07-23 A procedure for preparing linear alfaolephins. (Machine-translation by Google Translate, not legally binding)

Country Status (4)

Country Link
BE (1) BE684587A (en)
DE (1) DE1568461A1 (en)
ES (1) ES329470A1 (en)
NL (1) NL6610457A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1754694A1 (en) * 2005-08-10 2007-02-21 Linde AG Method for deactivation and removal of catalytic components in the oligomerisation of ethylene
EP1752433B1 (en) * 2005-08-10 2012-10-03 Linde AG Improved drying process for linear alpha-olefins
KR101679515B1 (en) 2015-02-12 2016-11-24 주식회사 엘지화학 Method of preparing catalyst system for oligomerization and catalyst sysyem for oligomerization prepared thereby

Also Published As

Publication number Publication date
BE684587A (en) 1967-01-25
NL6610457A (en) 1968-01-02
DE1568461A1 (en) 1970-03-19

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