GB621542A - Improvements in the manufacture of varnish resin interpolymers - Google Patents
Improvements in the manufacture of varnish resin interpolymersInfo
- Publication number
- GB621542A GB621542A GB4561/47A GB456147A GB621542A GB 621542 A GB621542 A GB 621542A GB 4561/47 A GB4561/47 A GB 4561/47A GB 456147 A GB456147 A GB 456147A GB 621542 A GB621542 A GB 621542A
- Authority
- GB
- United Kingdom
- Prior art keywords
- styrene
- oil
- mixture
- resins
- methyl styrene
- 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
- C08F212/00—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 aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
-
- 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
- C08F242/00—Copolymers of drying oils with other monomers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D125/00—Coating compositions based on homopolymers or 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 aromatic carbocyclic ring; Coating compositions based on derivatives of such polymers
- C09D125/02—Homopolymers or copolymers of hydrocarbons
- C09D125/04—Homopolymers or copolymers of styrene
- C09D125/08—Copolymers of styrene
- C09D125/14—Copolymers of styrene with unsaturated 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
- C08F212/00—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 aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/12—Monomers containing a branched unsaturated aliphatic radical or a ring substituted by an alkyl radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
A varnish resin is prepared by heating a mixture of (1) from 30 to 90 per cent by weight of a drying oil, free acid of a drying oil, or synthetic ester of a drying oil acid, which has a degree of conjugation not substantially exceeding that of dehydrated castor oil, and (2) from 70 to 10 per cent of a mixture of a polymerizable monovinyl aromatic compound and a nuclear alpha-methylene-lower alkyl aromatic compound, the alpha-methylene-lower alkyl group containing 3 or 4 carbon atoms and the mixture containing 50-80 per cent by weight of the monovinyl compound, to effect interpolymerization. Suitable drying oils are dehydrated castor oil, linseed, soyabean, perilla and fish oils. A mixture of one of these oils with a smaller proportion of a highly conjugated oil, e.g. tung oil, may be used. The monovinyl aromatic compound is preferably styrene, but o- and p-methyl styrene, o- and p-ethyl styrene, o-p-dimethyl styrene, p-chlorostyrene, p-methoxy styrene and vinyl naphthalene may be employed. Suitable alphamethylene-lower alkyl aromatic compounds are a -methyl styrene, p-methyl a -methyl styrene, a -ethyl styrene and p-chloro-a -methyl styrene. Polymerization may be effected by heating the mixture below boiling, e.g. 120-160 DEG C., with or without a catalyst such as benzoyl peroxide, acetyl benzoyl peroxide, tertiary butyl perbenzoate and tert.-butyl hydroperoxide. Alternatively, the drying oil is first heated to the polymerization temperature and the mixture of styrene or derivative and a -methyl styrene or derivative and catalyst is then added slowly over a period of several hours. Polymerization may also be effected in aqueous emulsion or in solution in, for example, diethyl benzene. The viscosity and hardness of the resins may be increased by heating at a temperature above 250 DEG C., but below their decomposition temperature, e.g. 275-295 DEG C. The resins are soluble in aromatic and aliphatic solvents and are compatible with linseed oil, most phenolic resins, some modified alkyd resins, rosin - esters, paracoumarone - indene, urea and melamine resins. The examples describe varnishes comprising the resins dissolved in mineral spirits/xylene and mineral spirits/toluene mixtures, with cobalt and manganese naphthenate driers and in one case containing guaiacol to prevent skinning; and an enamel made by adding titanium dioxide.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US649115XA | 1944-09-26 | 1944-09-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB621542A true GB621542A (en) | 1949-04-11 |
Family
ID=22059072
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4561/47A Expired GB621542A (en) | 1944-09-26 | 1947-02-17 | Improvements in the manufacture of varnish resin interpolymers |
GB33486/47A Expired GB649115A (en) | 1944-09-26 | 1947-12-18 | Improvements in or relating to the manufacture of varnish resin interpolymers |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB33486/47A Expired GB649115A (en) | 1944-09-26 | 1947-12-18 | Improvements in or relating to the manufacture of varnish resin interpolymers |
Country Status (1)
Country | Link |
---|---|
GB (2) | GB621542A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE899863C (en) * | 1949-08-26 | 1953-12-17 | Kurt Herbert & Co Vorm Otto Lo | Process for the production of copolymers |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE977088C (en) * | 1951-07-02 | 1965-01-28 | Burkhard Carlsohn | Process for the preparation of polymerization products |
-
1947
- 1947-02-17 GB GB4561/47A patent/GB621542A/en not_active Expired
- 1947-12-18 GB GB33486/47A patent/GB649115A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE899863C (en) * | 1949-08-26 | 1953-12-17 | Kurt Herbert & Co Vorm Otto Lo | Process for the production of copolymers |
Also Published As
Publication number | Publication date |
---|---|
GB649115A (en) | 1951-01-17 |
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