GB1092884A - Copolymers - Google Patents
CopolymersInfo
- Publication number
- GB1092884A GB1092884A GB23/65A GB2365A GB1092884A GB 1092884 A GB1092884 A GB 1092884A GB 23/65 A GB23/65 A GB 23/65A GB 2365 A GB2365 A GB 2365A GB 1092884 A GB1092884 A GB 1092884A
- Authority
- GB
- United Kingdom
- Prior art keywords
- copolymers
- methacrylate
- trimethyl
- vinyl
- methacrylic acid
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/20—Esters of polyhydric alcohols or phenols, e.g. 2-hydroxyethyl (meth)acrylate or glycerol mono-(meth)acrylate
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
Novel copolymers are derived from 2,2,4-trimethyl - 3 - hydroxypentyl methacrylate as essential component. The methacrylate is copolymerized with one or more other monomers such as styrene and its halogen and alkyl derivatives, vinylnaphthalene and halogen derivatives thereof, acrylonitrile, methacrylonitrile, vinyl esters, vinyl ethers, olefins, dienes, alkyl maleates and fumarates, vinyl and vinylidene halides, and aliphatic, alicyclic, aromatic and heterocyclic esters of acrylic or methacrylic acid. The copolymers may be obtained by dispersion, emulsion or solution polymerization methods using catalysts such as benzoyl, acetyl or hydrogen peroxide, cumene hydroperoxide, sodium, potassium or ammonium persulphate, possibly in a redox system, in some cases in the presence of dodecyl mercaptan. The copolymers are generally thermosetting and form hard films, for which purpose they may be admixed with, for example, melamine-formaldehyde resins.ALSO:2,2,4 - Trimethyl - 3 - hydroxypentyl methacrylate may be prepared by heating 2,2,4-trimethyl - 1,3 - pentanediol with methyl methacrylate in the presence of acidic or basic catalysts, e.g. sodium methoxide, optionally at reduced pressure and/or in the presence of excess methyl methacrylate or of an inert diluent, or by esterifying the aforementioned diol with methacrylic acid using an acidic catalyst. In either method an inhibitor such as hydroquinone is added to prevent polymerization. An example of the former method is given, the monomethacrylate ester being separated from dimethacrylate formed by distillation.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33566864A | 1964-01-03 | 1964-01-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1092884A true GB1092884A (en) | 1967-11-29 |
Family
ID=23312766
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23/65A Expired GB1092884A (en) | 1964-01-03 | 1965-01-01 | Copolymers |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR1432588A (en) |
GB (1) | GB1092884A (en) |
Cited By (7)
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 |
EP0594109A1 (en) * | 1992-10-19 | 1994-04-27 | Union Carbide Chemicals & Plastics Technology Corporation | Hindered-hydroxyl functional (meth)acrylate esters, copolymers containing them and compositions including same |
EP0646047A1 (en) * | 1991-04-19 | 1995-04-05 | Basf Corporation | Etch-resistant coating |
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 |
WO2003000434A1 (en) * | 2001-06-21 | 2003-01-03 | Basf Corporation | Basecoat composition comprising a poly(meth)acrylate binder |
WO2003027198A1 (en) * | 2001-09-27 | 2003-04-03 | Basf Corporation | Acryl clearcoat refinish composition |
-
1964
- 1964-12-30 FR FR344A patent/FR1432588A/en not_active Expired
-
1965
- 1965-01-01 GB GB23/65A patent/GB1092884A/en not_active Expired
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0646047A1 (en) * | 1991-04-19 | 1995-04-05 | Basf Corporation | Etch-resistant coating |
EP0646047A4 (en) * | 1991-04-19 | 1995-05-17 | Basf Corp | Etch-resistant coating. |
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 |
EP0594109A1 (en) * | 1992-10-19 | 1994-04-27 | Union Carbide Chemicals & Plastics Technology Corporation | Hindered-hydroxyl functional (meth)acrylate esters, copolymers containing them and compositions including same |
JPH06199953A (en) * | 1992-10-19 | 1994-07-19 | Union Carbide Chem & Plast Technol Corp | Copolymer containing hindered-hydroxyl-functional (meth)acrylate and composition containing same |
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 |
WO2003000434A1 (en) * | 2001-06-21 | 2003-01-03 | Basf Corporation | Basecoat composition comprising a poly(meth)acrylate binder |
US6794442B2 (en) | 2001-06-21 | 2004-09-21 | Basf Corporation | Fast drying basecoat refinish composition |
WO2003027198A1 (en) * | 2001-09-27 | 2003-04-03 | Basf Corporation | Acryl clearcoat refinish composition |
US7446149B2 (en) | 2001-09-27 | 2008-11-04 | Basf Corporation | Fast drying clearcoat refinish composition |
Also Published As
Publication number | Publication date |
---|---|
FR1432588A (en) | 1966-03-25 |
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