GB824312A - Ethylene polymerisation - Google Patents

Ethylene polymerisation

Info

Publication number
GB824312A
GB824312A GB15796/56A GB1579656A GB824312A GB 824312 A GB824312 A GB 824312A GB 15796/56 A GB15796/56 A GB 15796/56A GB 1579656 A GB1579656 A GB 1579656A GB 824312 A GB824312 A GB 824312A
Authority
GB
United Kingdom
Prior art keywords
tetrazene
bis
benzoyl
lauroyl peroxide
lauroyl
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
GB15796/56A
Inventor
John Carswell Mcgowan
Leslie Seed
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
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB15796/56A priority Critical patent/GB824312A/en
Publication of GB824312A publication Critical patent/GB824312A/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
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Ethylene is polymerized under super-atmospheric pressure and within a temperature range of 0-100 DEG C. in the presence of a catalyst comprising a mixture of a peroxy compound and an organic nitrogenous base in whose molecule the nitrogen atoms are not bonded directly to hydrogen atoms. Peroxy compounds include, di-t-butyl, lauroyl and benzoyl peroxides, di-isopropyl peroxydicarbonate, t-butyl perbenzoate, peracetic acid and cyclohexanone peroxide, and the nitrogen compounds may be tertiary amines, e.g. dimethylaniline; N-substituted heterocyclic secondary amines, e.g. N-ethyl piperidine, N-phenyl piperidine and N - methyl - 1,2,5,6 - tetrahydropyridine; N - alkyl pyrrolidines, N - alkyl hexamethylene imines and the corresponding N-alkenyl compounds; and tetrazenes, e.g. tetramethyltetrazene - 2, 1,4 - bis - cyclopentamethylene tetrazene - 2 and N,N1 - azomorpholine. A pressure range of between 200 and 2000 atmospheres preferably between 1000 and 1500 may be used and the ratio of peroxy to nitrogen compound in the mixture is preferably between 1 to 10 and 10 to 1 molar. A chain transfer agent, e.g. hydrogen, carbontetrachloride and chloroform may be present and the reaction may be in an inert liquid medium, e.g. benzene or water or a mixture thereof or in bulk except for an amount of solvent, e.g. white spirit, sufficient to dissolve the catalyst. In examples mixtures of benzoyl, lauroyl and diisopropyl peroxydicarbonate with dimethyl aniline; lauroyl peroxide and tetraethyl tetrazene-2; benzoyl and lauroyl peroxide with 1,4-bis-cyclopentamethylene tetrazene-2; lauroyl peroxide with 1,4-bis-(2-3-decahydrocyclopentamethylene) tetrazene-2; benzoyl and lauroyl peroxide with N-ethyl piperidine; lauroyl peroxide with N-methyl 1,2,5,6-tetrahydropyridine; and di-t-butyl peroxydicarbonate with 1,4-bis-cyclopentamethylene tetrazene-2 are used to produce solid polyethylene in improved yield.
GB15796/56A 1956-05-22 1956-05-22 Ethylene polymerisation Expired GB824312A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB15796/56A GB824312A (en) 1956-05-22 1956-05-22 Ethylene polymerisation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB15796/56A GB824312A (en) 1956-05-22 1956-05-22 Ethylene polymerisation

Publications (1)

Publication Number Publication Date
GB824312A true GB824312A (en) 1959-11-25

Family

ID=10065621

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15796/56A Expired GB824312A (en) 1956-05-22 1956-05-22 Ethylene polymerisation

Country Status (1)

Country Link
GB (1) GB824312A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3275615A (en) * 1962-12-28 1966-09-27 Union Carbide Corp Process for producing polyethylene in the presence of tertiary butyl hydroperoxide and n-butylamine
US3280095A (en) * 1962-12-28 1966-10-18 Union Carbide Corp Process for producing polyethylene
US4886861A (en) * 1985-04-23 1989-12-12 E. I. Dupont De Nemours And Company Molecular weight control in free radical polymerizations

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3275615A (en) * 1962-12-28 1966-09-27 Union Carbide Corp Process for producing polyethylene in the presence of tertiary butyl hydroperoxide and n-butylamine
US3280095A (en) * 1962-12-28 1966-10-18 Union Carbide Corp Process for producing polyethylene
US4886861A (en) * 1985-04-23 1989-12-12 E. I. Dupont De Nemours And Company Molecular weight control in free radical polymerizations

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