GB824312A - Ethylene polymerisation - Google Patents
Ethylene polymerisationInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements 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.
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)
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 |
-
1956
- 1956-05-22 GB GB15796/56A patent/GB824312A/en not_active Expired
Cited By (3)
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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