GB1110033A - Methacrylate polymers - Google Patents
Methacrylate polymersInfo
- Publication number
- GB1110033A GB1110033A GB34817/65A GB3481765A GB1110033A GB 1110033 A GB1110033 A GB 1110033A GB 34817/65 A GB34817/65 A GB 34817/65A GB 3481765 A GB3481765 A GB 3481765A GB 1110033 A GB1110033 A GB 1110033A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methacrylate
- methylstyrene
- acrylate
- methyl
- trimethyl
- 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
- C08F22/00—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 a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F22/10—Esters
- C08F22/1006—Esters of polyhydric alcohols or polyhydric phenols, e.g. ethylene glycol dimethacrylate
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
Copolymers are formed from 2,2,4-trimethylpentyl-1,3 -dimethacrylate (TMPD) and at least one other vinylidene or vinyl monomer. Specified comonomers are styrene, o-methylstyrene, m-methylstyrene, 2,4-dimethyl styrene, o-ethylstyrene, vinyl chloride, vinylidene chloride, acrylonitrile, 2,2,4-trimethyl-3-hydroxypentyl methacrylate and esters of formula <FORM:1110033/C3/1> wherein R1 is hydrogen or methyl and R is an alkyl group of 1 to 8 carbon atoms, an alicyclic group of 4 to 8 carbon atoms or an aryl or aralkyl group of 6 to 12 carbon atoms. For example R may be a cyclobutyl, cyclopentyl, phenyl, a -naphthyl or b -naphthyl group. The monomers are heated together to e.g. 40 DEG to 160 DEG C. The mixture may be cast into a film or mould either before heating or after partial reaction. In the latter case the copolymer may be cured by heating after casting. The monomer other than T.M.P.D. may be partially polymerized prior to addition of the T.M.P.D. In Example 1 a copolymer of T.M.P.D. and methyl methacrylate is prepared by polymerizing the latter to about 25% conversion and reacting the T.M.P.D. with the resulting syrup; in Example II 2,2,4 - trimethyl - 3 - hydroxypentyl methacrylate is also added to the methyl methacrylate syrup. In other examples terpolymers of T.M.P.D., (1) methyl methacrylate and (2) methyl acrylate, (3) ethyl acrylate, (4) n-butyl methacrylate, (5) n-butyl acrylate, (6) isobutyl acrylate, (7) 2-ethylhexyl methacrylate, (8) 2-ethylhexyl acrylate, (9) ethyl methacrylate and (10) isopropyl methacrylate are prepared. Copolymers of T.M.P.D. and (12) styrene, (13) o-methylstyrene, (14) m-methylstyrene, (15) 2,4-dimethylstyrene, (16) o-ethylstyrene, (17) vinyl chloride, (18) acrylonitrile and (19) vinylidene chloride are produced by reacting the monomers with t.-bu. hydroperoxide as catalyst. In Example 20 T.M.P.D. and 2,2,4-trimethyl-3-hydroxypentyl methacrylate are copolymerized using benzoyl peroxide as catalyst. In Examples 21 and 22 the comonomer is (21) cyclohexyl methacrylate and (22) a -phenylethyl methacrylate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US38947664A | 1964-08-13 | 1964-08-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1110033A true GB1110033A (en) | 1968-04-18 |
Family
ID=23538421
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB34817/65A Expired GB1110033A (en) | 1964-08-13 | 1965-08-13 | Methacrylate polymers |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1455276A (en) |
GB (1) | GB1110033A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5290602A (en) * | 1992-10-19 | 1994-03-01 | Union Carbide Chemicals & Plastics Technology Corporation | Hindered-hydroxyl functional (meth) acrylate-containing copolymers particularly suitable for use in coating compositions which are sprayed with compressed fluids as viscosity reducing diluents |
US5420341A (en) * | 1992-10-19 | 1995-05-30 | Union Carbide Chemicals & Plastics | Hindered-hydroxyl functional (meth)acrylate compounds and processes for the preparation thereof |
US5442023A (en) * | 1994-06-30 | 1995-08-15 | Union Carbide Chemicals & Plastics Technology Corporation | Hindered-hydroxyl functional (meth)acrylate monomers containing di(meth)acrylates and compositions including same |
-
1965
- 1965-08-05 FR FR27316A patent/FR1455276A/en not_active Expired
- 1965-08-13 GB GB34817/65A patent/GB1110033A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5290602A (en) * | 1992-10-19 | 1994-03-01 | Union Carbide Chemicals & Plastics Technology Corporation | Hindered-hydroxyl functional (meth) acrylate-containing copolymers particularly suitable for use in coating compositions which are sprayed with compressed fluids as viscosity reducing diluents |
US5420341A (en) * | 1992-10-19 | 1995-05-30 | Union Carbide Chemicals & Plastics | Hindered-hydroxyl functional (meth)acrylate compounds and processes for the preparation thereof |
US5442023A (en) * | 1994-06-30 | 1995-08-15 | Union Carbide Chemicals & Plastics Technology Corporation | Hindered-hydroxyl functional (meth)acrylate monomers containing di(meth)acrylates and compositions including same |
Also Published As
Publication number | Publication date |
---|---|
FR1455276A (en) | 1966-04-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1197323A (en) | Polymers containing Sulphonic Acid Groups | |
GB1034753A (en) | A process for the production of polymers of conjugated dienes | |
US4328329A (en) | Process for polymerizing methyl methacrylate syrup using a dual initiator system | |
GB1437176A (en) | Acrylic copolymers | |
GB1194950A (en) | Process of preparing Methyl Methacrylate Polymers | |
GB1045229A (en) | Foamable thermoplastic synthetic resins | |
Gilath et al. | Copolymerization of styrene. IV. Copolymerization with esters of benzylidenecyanoacetic acid | |
GB1138593A (en) | Methyl methacrylate polymer and process for making same | |
GB1110033A (en) | Methacrylate polymers | |
GB1041088A (en) | Improvements in or relating to the preparation of linear peroxy-group-containing copolymers | |
GB1326748A (en) | Acrylate terpolymer resin binder for photoelectrostatic members | |
US3198775A (en) | Copolymers having improved optical clarity | |
GB765520A (en) | Improvements in interpolymer compounds | |
JPS5922725B2 (en) | Method of manufacturing syrup | |
GB1401768A (en) | Polymerisable unsaturated oxazolidines and tetrahydro-1,3-oxa zines and polymers thereof | |
US3634367A (en) | Thermally stabilized acrylic polymers | |
SE319607B (en) | ||
JP3061551B2 (en) | Method for producing methacrylic resin | |
GB836755A (en) | Improvements in and relating to polymers | |
GB1355679A (en) | Production of mouldable and or thermoformable polymers | |
GB665005A (en) | Improvements in the manufacture of interpolymers | |
GB1005204A (en) | Polymerisation of vinyl monomers | |
GB1235752A (en) | Process for preparing copolymers of vinyl-aromatic and maleic monomers | |
GB833585A (en) | Improvements in preparation of graft polymers | |
GB1459058A (en) | Stable heat-sensitive latex mixtures |