GB949054A - Improvements relating to the polymerisation of unsaturated esters - Google Patents
Improvements relating to the polymerisation of unsaturated estersInfo
- Publication number
- GB949054A GB949054A GB2772360A GB2772360A GB949054A GB 949054 A GB949054 A GB 949054A GB 2772360 A GB2772360 A GB 2772360A GB 2772360 A GB2772360 A GB 2772360A GB 949054 A GB949054 A GB 949054A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alcohol
- aluminium
- methyl
- ethyl
- esters
- 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
- C08F18/00—Homopolymers 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 acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid
- C08F18/02—Esters of monocarboxylic acids
- C08F18/04—Vinyl esters
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
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)
- Polymerization Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Polymers of vinyl esters e.g. vinyl acetate, and esters of acrylic acids are made by subjecting the ester to the action of a catalyst consisting essentially of a trialkyl aluminium or dialkyl aluminium chloride in which the alkyl groups have 1 to 8 carbon atoms, and an alcohol which is either an alkenol in which the unsaturation is more than 2 carbon atoms removed from the hydroxyl group, or an alkanol of the formula CnHm(OH)x, where n=1 to 4, m=2n+2-x and x=1, 2, or 3, and which contains in solution 0.004-0.04 cc. of oxygen (as measured at 0 DEG C. and 760 mm. of pressure) per cc. of alcohol. The polymerization is preferably effected in an inert hydrocarbon or halogensubstituted hydrocarbon medium. The esters of acrylic acid may be ethylene glycol dimethacrylate, polyethylene glycol dimethacrylate, methyl methacrylate, methyl alphaethacrylate, ethyl alphapropacrylate, propylene glycol di-alpha-ethacrylate, ethyl alphaphenylacrylate, methyl alpha-chloroacrylate, ethyl alpha-cyclohexylacrylate, or methyl alphadecylacrylate. The preferred aluminium alkyls are trimethyl, triethyl, tripropyl, triisopropyl, tributyl, triamyl, triisoamyl, trihexyl, triisohexyl, triheptyl, and trioctyl aluminium and the corresponding dialkyl aluminium chlorides. The alcohol may be oleyl alcohol, undecylenyl alcohol, 4-hexen -1- ol, 1-penten -5-ol, 4-octen -1- ol, 3-buten -1- ol, methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, isobutyl alcohol, 2-butanol, t-butyl alcohol, amyl alcohol, isoamyl alcohol, t-amyl alcohol, s-amyl alcohol, n-hexyl alcohol, n-heptyl alcohol, n-octyl alcohol, n-nonyl alcohol, n-decyl alcohol, n-undecyl alcohol, lauryl alcohol and myristyl alcohol. When the alcohols are commercial products they all contain dissolved oxygen in amounts within the range previously specified. The polymers are purified by conventional techniques e.g. methanol and/or aqueous hydrochloric acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US710660A | 1960-02-08 | 1960-02-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB949054A true GB949054A (en) | 1964-02-12 |
Family
ID=21724248
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2772360A Expired GB949054A (en) | 1960-02-08 | 1960-08-10 | Improvements relating to the polymerisation of unsaturated esters |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1157784B (en) |
FR (1) | FR1276544A (en) |
GB (1) | GB949054A (en) |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE878560C (en) * | 1950-06-22 | 1953-06-05 | Karl Dr Ziegler | Process for the polymerization and interpolymerization of olefins |
-
1960
- 1960-08-09 DE DE1960G0003025 patent/DE1157784B/en active Pending
- 1960-08-10 GB GB2772360A patent/GB949054A/en not_active Expired
- 1960-12-22 FR FR847764A patent/FR1276544A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1157784B (en) | 1963-11-21 |
FR1276544A (en) | 1961-11-17 |
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