GB795177A - Improvements in polymerization of hydrocarbons and catalyst therefor - Google Patents

Improvements in polymerization of hydrocarbons and catalyst therefor

Info

Publication number
GB795177A
GB795177A GB6335/56A GB633556A GB795177A GB 795177 A GB795177 A GB 795177A GB 6335/56 A GB6335/56 A GB 6335/56A GB 633556 A GB633556 A GB 633556A GB 795177 A GB795177 A GB 795177A
Authority
GB
United Kingdom
Prior art keywords
olefines
halide
catalyst
tetra
polymerization
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
GB6335/56A
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.)
Phillips Petroleum Co
Original Assignee
Phillips Petroleum 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 Phillips Petroleum Co filed Critical Phillips Petroleum Co
Publication of GB795177A publication Critical patent/GB795177A/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
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • 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
    • C08F36/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F36/02Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F36/04Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A catalyst for polymerizing olefines consist of a mixture of an organo-metal halide and a tri-halide or tetra-halide of a Group IV metal. The organo-metal halide is of the tppe RnMXy, in which R is alkyl, aryl, or saturated cyclic radical; M is aluminium, gallium, indium, thallium, or beryllium; X is halogen. The second component is a tri- or tetra-halide of titanium, silicon, thorium, zirconium, tin, lead, hafnium, germanium, or cerium. The catalyst is effective at low temperatures, the range specified being -250 DEG to +500 DEG F., and preferably -125 DEG to 200 DEG F. Polymerization may be effected under pressure, and in the presence of solvents, e.g. cycloparaffins, or aromatic hydrocarbons. A preferred catalyst mixture consists of diethyl aluminium chloride or ethyl aluminium dichloride and titanium or zirconium tetrachloride or tetrabromide. A number of examples are given including, as the first catalyst component, organic radicals containing up to 20 carbon atoms, e.g. cyclohexene gallium or indium chloride, C17H35BeI and C20H41GaBr2. Olefines polymerized are: 1-olefines containing up to 8 carbon atoms; branched chain or polyolefines with non-conjugated double bonds, cyclic olefines or aryl olefines. Co-polymers are referred to.ALSO:Olefines are polymerized with a catalyst consisting of a mixture of an organo-metallic halide and a tri-halide or tetra-halide of a Group IV metal, e.g. in the mol. ratio of 0.05 to 20 : 1. The organo-metallic halide is of the type RnMXy in which R is alkyl, aryl or a saturated cyclic radical; M is aluminium, gallium, indium, thallium or beryllium and X is halogen. The second component is a tri- or tetra-halide of titanium, silicon, thorium, zirconium, tin, lead, hafnium, germanium or cerium. A preferred mixture consists of diethyl aluminium chloride or ethyl aluminium dichloride with titanium or zirconium tetra chloride or tetra bromide. A number of compounds are specified including, as the first component, organic radicals containing up to 20 carbon atoms, e.g. cyclohexene gallium or indium chloride, C17H35BeI and C20H41GaBr2. Polymerization may be effected in the gaseous state or in the presence of solvents such as propane, butane, pentane, iso-octane, cyclohexane, methylcyclohexane, benzene and toluene, and in the temperature range -250 DEG to +500 DEG F., preferably at -125 DEG to +200 DEG F. Olefines polymerized are: 1-olefines containing up to 8 carbon atoms; branched chain or polyolefines with non-conjugated double bonds; cyclic olefines or aryl olefines, and specified are ethylene, propylene, butene, hexene, octene, isobutylene, alkyl substituted ethylenes, hexatriene, pentadiene, octatriene, cyclohexene, styrene and alkyl substituted styrenes. Copolymers are referred to. The monomers and/or the diluent are desirably freed before use from catalyst poisons, e.g. with the use of alkaline pyrogallol. The polymerization may be batchwise or by continuous flow, and further olefin may be added continuously or intermittently. Following polymerization the catalyst may be destroyed and the product purified by treatment with alcohols, such as isopropyl and butyl alcohols. In Example IV the temperature used ranges from -45 DEG to -67 DEG F. The polymers are of high density and may be moulded to form articles such as bottles, piping and tubing.
GB6335/56A 1955-03-17 1956-02-29 Improvements in polymerization of hydrocarbons and catalyst therefor Expired GB795177A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US795177XA 1955-03-17 1955-03-17

Publications (1)

Publication Number Publication Date
GB795177A true GB795177A (en) 1958-05-21

Family

ID=22151067

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6335/56A Expired GB795177A (en) 1955-03-17 1956-02-29 Improvements in polymerization of hydrocarbons and catalyst therefor

Country Status (2)

Country Link
FR (1) FR1147588A (en)
GB (1) GB795177A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3070590A (en) * 1958-08-02 1962-12-25 Distillers Co Yeast Ltd Three component inorganic catalyst for the polymerization of ethylene

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3111511A (en) * 1959-04-06 1963-11-19 Grace W R & Co Polymerization of ethylene with aluminum alkyl-rare earth halide catalysts

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3070590A (en) * 1958-08-02 1962-12-25 Distillers Co Yeast Ltd Three component inorganic catalyst for the polymerization of ethylene

Also Published As

Publication number Publication date
FR1147588A (en) 1957-11-27

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