GB942297A - Poly(4-methyl-pentene-1) and articles produced therefrom - Google Patents

Poly(4-methyl-pentene-1) and articles produced therefrom

Info

Publication number
GB942297A
GB942297A GB2269561A GB2269561A GB942297A GB 942297 A GB942297 A GB 942297A GB 2269561 A GB2269561 A GB 2269561A GB 2269561 A GB2269561 A GB 2269561A GB 942297 A GB942297 A GB 942297A
Authority
GB
United Kingdom
Prior art keywords
polymer
ashing
slurry
medium
liquid
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
GB2269561A
Inventor
Keith Jasper Clark
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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
Priority to BE619296D priority Critical patent/BE619296A/xx
Priority to NL280043D priority patent/NL280043A/xx
Priority to NL133100D priority patent/NL133100C/xx
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2269561A priority patent/GB942297A/en
Priority to DE1962J0021965 priority patent/DE1520101B2/en
Priority to FR901697A priority patent/FR1331635A/en
Priority to JP2557962A priority patent/JPS5270B1/ja
Priority to DK280362A priority patent/DK109758C/en
Publication of GB942297A publication Critical patent/GB942297A/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
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond

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)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

A polymer of 4-methyl-pentene-1 is prepared by polymerizing the monomer under air and moisture-free conditions in the presence of a stereospecific catalyst, and as diluent an inert hydrocarbon liquid, excess of the monomer itself or a chlorinated aromatic hydrocarbon, whereby a separable slurry of poly-4-methyl-pentene-1 is diluent is obtained and then de-ashing the polymer under water-free conditions so that the ash content does not exceed 0.1% by weight of the polymer and the transition metal content of the polymer is below 50 p.p.m. In the de-ashing operation, the slurry or its dispersed polymer content is treated with sufficient of an effective reagent to react with all of the catalyst residues to convert them to products soluble in the liquid medium, then the polymer is washed at least until all visible colour has been removed and finally the polymer is separated from the residual wash liquid. The polymer obtained has a melting point of 243 DEG C., a melt flow index between 0.01 and 1000, a density of 0.82 to 0.86 g/cc. and can be melt shaped into shaped articles having in 1/8 inch section a clarity of grade 1 and a haze of group 1. Suitable liquid media for the de-ashing step include (a) the dispersion phase of the slurry (including any unreacted reagent plus any other organic solvent which may be added), (b) if the dispersed polymer has previously been separated from the dispersion phase of the slurry, the liquid media may be any unreacted reagent plus any other organic solvent which might have been added to the polymer and any of the dispersion phase of the slurry occluded with the dispersed polymer. If the medium is primarily hydrocarbon, the higher alcohols, higher acids and higher amines (e.g. carbon chain of at least 8 carbon atoms) may be employed as the de-ashing reagents. e.g. 3,5,5-trimethylhexanol dodecanol, n-nonoic acid and 3,5,5-trimethylhexylamine may be used. Mixtures of acetyl acetone and isopropylalcohol may also be used. If the medium is primarily a polar one, lower alcohols may be used both as the reagent and as the medium. Numerous examples are given in which the stereospecific catalysts are selected from TiCl3 with AL(C2H5)2 Cl, LiC4H9, Zn(C4H9)2, AL(C2H5)3, AL(iso-C4H9)3, lithium aluminium butyl triethyl or with aluminium ethyl sesquichloride. The de-ashing agents are selected from acetylacetone with n-butanol or isopropyl alcohol; n-butanol; isopropanol; nonanol; ethanol; methanol; n-dodecanol; n-nonoic acid; 3,5,5 trimethylhexylamine; 3,5,5 trimethylhexanol and acetyl acetone. The washing medium is preferably a water-free organic liquid. In some examples, alcohols e.g. methanol, ethanol, isopropanol, butanol and nonanol, are used both as the de-ashing reagent and as the washing agent. Shaped articles may be produced from the polymers by the usual processes. Specifications 789,781, 808,144, 821,634, 877,050 and 940,145 are referred to.
GB2269561A 1961-06-22 1961-06-22 Poly(4-methyl-pentene-1) and articles produced therefrom Expired GB942297A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
BE619296D BE619296A (en) 1961-06-22
NL280043D NL280043A (en) 1961-06-22
NL133100D NL133100C (en) 1961-06-22
GB2269561A GB942297A (en) 1961-06-22 1961-06-22 Poly(4-methyl-pentene-1) and articles produced therefrom
DE1962J0021965 DE1520101B2 (en) 1961-06-22 1962-06-20 PROCESS FOR MANUFACTURING CLEAR, CRYSTALLINE POLY-4-METHYLPENTENE
FR901697A FR1331635A (en) 1961-06-22 1962-06-22 Production and applications of new crystalline polymers of 4-methyl-pentene-1
JP2557962A JPS5270B1 (en) 1961-06-22 1962-06-22
DK280362A DK109758C (en) 1961-06-22 1962-06-22 Process for the preparation of a polymer of 4-methylpentene-1, which can be formed by melting into objects with high transparency.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB2269561A GB942297A (en) 1961-06-22 1961-06-22 Poly(4-methyl-pentene-1) and articles produced therefrom
GB4303461 1961-12-01

Publications (1)

Publication Number Publication Date
GB942297A true GB942297A (en) 1963-11-20

Family

ID=26256068

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2269561A Expired GB942297A (en) 1961-06-22 1961-06-22 Poly(4-methyl-pentene-1) and articles produced therefrom

Country Status (6)

Country Link
JP (1) JPS5270B1 (en)
BE (1) BE619296A (en)
DE (1) DE1520101B2 (en)
DK (1) DK109758C (en)
GB (1) GB942297A (en)
NL (2) NL133100C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3327050A (en) * 1964-07-29 1967-06-20 Ici Ltd Cables with 4-methyl pentene-1 primary insulation
CN115612005A (en) * 2022-11-09 2023-01-17 山东京博石油化工有限公司 Efficient solvent deashing treatment method for polypropylene resin

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3327050A (en) * 1964-07-29 1967-06-20 Ici Ltd Cables with 4-methyl pentene-1 primary insulation
CN115612005A (en) * 2022-11-09 2023-01-17 山东京博石油化工有限公司 Efficient solvent deashing treatment method for polypropylene resin

Also Published As

Publication number Publication date
NL280043A (en)
NL133100C (en)
DE1520101A1 (en) 1970-03-19
DK109758C (en) 1968-06-24
JPS5270B1 (en) 1977-01-05
BE619296A (en)
DE1520101B2 (en) 1976-11-04

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