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GB817308A - Novel catalyst composition, preparation and use thereof - Google Patents

Novel catalyst composition, preparation and use thereof

Info

Publication number
GB817308A
GB817308A GB20131/57A GB2013157A GB817308A GB 817308 A GB817308 A GB 817308A GB 20131/57 A GB20131/57 A GB 20131/57A GB 2013157 A GB2013157 A GB 2013157A GB 817308 A GB817308 A GB 817308A
Authority
GB
United Kingdom
Prior art keywords
compounds
catalyst
aluminium
vinyl
olefins
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
GB20131/57A
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.)
MW Kellogg Co
Original Assignee
MW Kellogg 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 MW Kellogg Co filed Critical MW Kellogg Co
Publication of GB817308A publication Critical patent/GB817308A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08F4/00Polymerisation catalysts
    • C08F4/42Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
    • C08F4/44Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
    • C08F4/52Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides selected from boron, aluminium, gallium, indium, thallium or rare earths
    • 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
    • C08F16/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
    • C08F16/12Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A catalyst for the polymerization of olefins comprises (i) an organo-metallic compound of a metal of Group IIIb, e.g. tri-ethyl aluminium, (ii) a halide of a metal of Groups IVa, Va, VIa, VIIa or VIII, e.g. titanium tetrachloride, and (iii) a chlorine-substituted organic compound, e.g. carbon tetrachloride or trichloroethylene. The catalyst is prepared by independently adding the organo-metallic compound and the inorganic metal halide to the chlorine-substituted organic compound in the absence of air and moisture, whereby a red liquid complex is formed. A stable liquid catalyst is obtained by also having a hydrocarbon, e.g. hexane, present when the starting materials are independently mixed. The presence of the hydrocarbon is unnecessary when the chlorine-substituted organic compound is carbon tetrachloride. Preferred chlorine-substituted organic compounds may be aliphatic or aromatic and include methylene dichloride, chloroform, carbon tetrachloride, trichloroethylene, tetrachloroethylene, tetrachloroethane, pentachloroethane and chlorobenzene. Some preferred metal compounds of Group IIIb are trimethyl aluminium, triethyl aluminium, tri-isobutyl aluminium, aluminium tri-n-hexyl, trimethyl indium, diethyl aluminium fluoride, ethyl aluminium dihydride. The preferred inorganic metal chlorides are titanium tetrachloride, zirconium tetrachloride and ferric chloride. The polymers produced by the catalysts may be derived from substituted or unsubstituted olefins including vinyl compounds and organic compounds having at least one ethylenic carbonto-carbon double bond, including both acyclic and alicyclic compounds.ALSO:Vinyl-type compounds, i.e. compounds having at least one ethylenic carbon-to-carbon double bond, including both acyclic and alicyclic compounds, are polymerized at a temperature of -100 DEG to 200 DEG C., preferably at -20 DEG to 100 DEG C., in the presence of a catalyst comprising (i) an organo-metallic compound of a metal of Group IIIb, e.g. tri-ethyl aluminium, (ii) a halide of a metal of Groups IVa, Va, VIa, VIIa or VIII, e.g. titanium tetrachloride, and (iii) a chlorine-substituted organic compound, e.g. carbon tetrachloride or trichlorethylene (see Group III). The catalysts are liquid and stable, although stability may be further improved by adding n-hexane. Hence polymerization may be effected in a homogeneous liquid phase and so is easier to control, can be carried out in a simplified apparatus, and the polymer does not become occluded within the catalyst and may be freed from catalyst by simple washing. Vinyl-type compounds which may be polymerized include aliphatic mono-olefins of up to 20 DEG C. atoms, e.g. ethylene, aliphatic polyolefins such as conjugated dienes, e.g. butadiene, halogen-substituted olefins, e.g. vinyl chloride, alkoxy and aryl substituted olefins, e.g. vinyl ethly ether, and monomers containing any combination of halogen, alkoxy and aryl substituents, e.g. phenyltrifluoroethylene. The polymerization is preferably carried out between -20 DEG and 65 DEG C., under pressures of 1-1000 atmospheres and ethylene may be polymerized at room temperature and atmospheric pressure by simply passing it through the catalyst in an open vessel. Examples describe the polymerization of: (Ex. 2-4) trifluorochloroethylene, (Ex. 11) ethylene, (Ex. 12) propylene, (Ex. 14) isobutylene, (Ex. 15) 2-olefins, (Ex. 16, 17) copolymerization of ethylene and propylene, (Ex. 18) butadiene-1,3, (Ex. 19) vinyl chloride, (Ex. 20) styrene, (Ex. 21) vinyl isobutyl ether, (Ex. 22, 23) ethylene, (Ex. 24) 1,1,3-trifluorobutadiene.
GB20131/57A 1956-07-02 1957-06-26 Novel catalyst composition, preparation and use thereof Expired GB817308A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US817308XA 1956-07-02 1956-07-02

Publications (1)

Publication Number Publication Date
GB817308A true GB817308A (en) 1959-07-29

Family

ID=22166022

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20131/57A Expired GB817308A (en) 1956-07-02 1957-06-26 Novel catalyst composition, preparation and use thereof

Country Status (1)

Country Link
GB (1) GB817308A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1164096B (en) * 1962-05-02 1964-02-27 Bayer Ag Process for the production of polybutadiene
DE1253917B (en) * 1965-05-24 1967-11-09 Bayer Ag Process for the solution polymerization of isoprene
DE1292844B (en) * 1964-11-10 1969-04-17 Bayer Ag Process for the polymerization of isoprene

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1164096B (en) * 1962-05-02 1964-02-27 Bayer Ag Process for the production of polybutadiene
DE1292844B (en) * 1964-11-10 1969-04-17 Bayer Ag Process for the polymerization of isoprene
DE1253917B (en) * 1965-05-24 1967-11-09 Bayer Ag Process for the solution polymerization of isoprene

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