GB581170A - Copolymers - Google Patents
CopolymersInfo
- Publication number
- GB581170A GB581170A GB436342A GB436342A GB581170A GB 581170 A GB581170 A GB 581170A GB 436342 A GB436342 A GB 436342A GB 436342 A GB436342 A GB 436342A GB 581170 A GB581170 A GB 581170A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fusible
- methyl
- polymers
- ethyl
- polymer
- 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
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers 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
- C08F36/20—Homopolymers 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 unconjugated
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
An infusible and insoluble polymer is prepared by polymerizing a mixture of a fusible heat-convertible polymer of an organic oxygen compound containing at least two polymerizable groups and another compound containing at least one of said groups. The fusible polymers may be prepared as described in Specifications 536,807, 540,938 and 540,939. In addition, the polymers made from mono or diisopropenyl carbonate, phthalate, crotonate, maleate, acrylate, malonate or oxalate may be used. Further, the fusible polymer may be prepared as described in Specifications 578,266 and 578,267. The other compound may be vinyl acetate, vinyl chloride, acrylic or a -substituted acrylic acids, methyl, ethyl, propyl, butyl, amyl and lauryl acrylates, methacrylates ethacrylates or a -chloro-acrylates glycol and glycerol monoacrylates or monomethacrylates, glycerol monochloroacrylate, resorcinol monomethacrylate; allyl or crotyl acetate, chloride, benzoate and alcohol; methallyl chloride, acetate, butyrate and benzoate; styrene, vinyl ethyl ether, ethyl allyl ether; methyl, ethyl, propyl, butyl or amyl crotonates, chlorocrotonates, cinnamates or tiglates, methyl, ethyl, propyl or butyl maleates or fumarates; monomethylallyl, monoallyl or monocrotyl phthalates, citrates, tartrates, silicates, adipates, glutarates, lactates, glycollates, suberates, succinates, phosphates, phosphites, sulphates, sulphites or sulphides; butadiene and chlorobutadiene. Mixtures of fusible, heat-convertible polymers, or such polymers incorporated in a monomer capable of forming such polymers may be further polymerized. Preferably, the composition resulting from the polymerization of monomer is concentrated to increase the proportion of fusible polymer relative to monomer. The further polymerization may be catalysed by oxygen, ozone or peroxides under heat, light or pressure. The catalyst may be formed in situ by oxidizing the monomer or polymer by passing air or oxygen through their solutions. In a typical example, a solution of allyl methacrylate and benzoyl peroxide in acetone was refluxed at 63 DEG C. for three hours. Methyl alcohol was added and the mixture added, with stirring, to a methyl alcohol-water mixture. The precipitate of fusible polyallyl methacrylate was mixed with methyl methyacrylate and benzoyl peroxide and heated in a mould at 65 DEG C. for 17 hours. The product was further heated at 100 DEG C. for eight hours to produce an insoluble material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB436342A GB581170A (en) | 1942-04-01 | 1942-04-01 | Copolymers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB436342A GB581170A (en) | 1942-04-01 | 1942-04-01 | Copolymers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB581170A true GB581170A (en) | 1946-10-03 |
Family
ID=9775756
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB436342A Expired GB581170A (en) | 1942-04-01 | 1942-04-01 | Copolymers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB581170A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2615864A (en) * | 1947-06-21 | 1952-10-28 | Socony Vacuum Oil Co Inc | Esterified allyl ester-polycarboxylic acid copolymers |
US5070140A (en) * | 1989-12-22 | 1991-12-03 | Basf Corporation | Copolymers of vinyl acetate and allyl glycidyl ether capped C12 -C.sub. |
US5480954A (en) * | 1994-09-21 | 1996-01-02 | Arco Chemical Technology, L.P. | Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols |
US5605995A (en) * | 1994-09-21 | 1997-02-25 | Arco Chemical Technology, L.P. | Hydroxy-functional allyl terpolymers |
-
1942
- 1942-04-01 GB GB436342A patent/GB581170A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2615864A (en) * | 1947-06-21 | 1952-10-28 | Socony Vacuum Oil Co Inc | Esterified allyl ester-polycarboxylic acid copolymers |
US5070140A (en) * | 1989-12-22 | 1991-12-03 | Basf Corporation | Copolymers of vinyl acetate and allyl glycidyl ether capped C12 -C.sub. |
US5480954A (en) * | 1994-09-21 | 1996-01-02 | Arco Chemical Technology, L.P. | Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols |
US5519103A (en) * | 1994-09-21 | 1996-05-21 | Arco Chemical Company | Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols |
US5569714A (en) * | 1994-09-21 | 1996-10-29 | Arco Chemical Technology, L.P. | Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols |
US5605995A (en) * | 1994-09-21 | 1997-02-25 | Arco Chemical Technology, L.P. | Hydroxy-functional allyl terpolymers |
US5639827A (en) * | 1994-09-21 | 1997-06-17 | Arco Chemical Technology, L.P. | Allyl ester copolymers with allylic alcohols or propoxylated allylic alcohols |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2464062A (en) | Polymerization with a peroxydicar-bonate catalyst | |
US2680109A (en) | Allyl-2, 3-epoxybutyrate | |
US2580901A (en) | Copolymer of styrene, glycidyl acrylate, and glycidyl methacrylate | |
US2379218A (en) | Method of casting resins | |
US2332460A (en) | Polymerized esters of polymeric unsaturated alcohols and method of manufacture thereof | |
US2405817A (en) | Copolymer of styrene and fusible partial polymer of divinyl benzene | |
US2431374A (en) | Copolymers of diallyl maleate and saturated monohydric alcohol esters of maleic and fumaric acids | |
US2520601A (en) | Polymerization promoters | |
US2394642A (en) | Silicic acid esters | |
US2444655A (en) | Abrasion-resistant polymers and process for preparing same | |
US2370572A (en) | Unsaturated esters and polymers thereof | |
GB581170A (en) | Copolymers | |
US2504082A (en) | Acrylic esters of alkoxy-3-butenols and polymers therefrom | |
US2384119A (en) | Unsaturated esters | |
GB536807A (en) | Method of producing fusible acrylate polymers, and infusible polymers therefrom | |
US3249574A (en) | Polyester-vinyl monomer compositions containing hydrogen peroxide | |
US2441516A (en) | Interpolymers of allylic alcohol and allylic acrylates | |
US2258423A (en) | Polymerization of alpha, beta, unsaturated polycarboxylic acid esters of polyhydric alcohols with vinyl compounds | |
US2279882A (en) | Interpolymers of di-(methoxyethyl) itaconate and ethyl methacrylate | |
US2384117A (en) | Unsaturated esters and polymers thereof | |
GB491894A (en) | Improvements in or relating to esters of acrylic acid and polymerisation products thereof | |
US2401581A (en) | Unsaturated esters and polymers thereof | |
US2877208A (en) | Acrylate monomers and polymers of tetrahydropyran methyl alcohol | |
GB471755A (en) | Improvements in or relating to the polymerisation of methacrylic acid esters | |
GB1015619A (en) | Improvements in or relating to vinylaromatic polymer preparation |