GB794585A - Process for the manufacture of raw materials for lacquers - Google Patents
Process for the manufacture of raw materials for lacquersInfo
- Publication number
- GB794585A GB794585A GB2060155A GB2060155A GB794585A GB 794585 A GB794585 A GB 794585A GB 2060155 A GB2060155 A GB 2060155A GB 2060155 A GB2060155 A GB 2060155A GB 794585 A GB794585 A GB 794585A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyhydric alcohols
- isocyanate
- isocyanates
- interesterification
- acids
- 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
- 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
- C09D155/00—Coating compositions based on homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C09D123/00 - C09D153/00
- C09D155/04—Polyadducts obtained by the diene synthesis
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Mixed esters of polyhydric alcohols and polybasic acids and containing unsaturated fatty acid radicals are polymerized with unsaturated compounds containing at least one -CH=CHR group where R is hydrogen or a hydrocarbon residue, the product interesterified with polyhydric alcohols and reacted with isocyanates or diisocyanates. The mixed esters may be derived from polycarboxylic acids, e.g. succinic, glutaric, adipic, phthalic, maleic, tricarballylic and citric acids or their anhydrides, polyhydric alcohols, e.g. glycol, diethylene glycol, propanediols, butanediols, hexanediols, heptanediols, glycerol, trimethylol propane, trimethylol ethane, hexanetriol, pentaerythritol, sorbitol and mannitol, and unsaturated fatty acids or their glycerides, e.g. linseed, perilla, dehydrated castor, soya, groundnut, poppyseed, liver, pilchard, menhaden, fish, wood and oiticica oils. Specified unsaturated compounds are vinyl chloride, vinyl acetate, acrylic and methacrylic esters, styrene, a -methyl styrene, dichlorostyrene, divinyl benzene, indene, coumarone, butadiene, isoprene, cyclohexadiene, cyclopentadiene and dicyclopentadiene. The interesterification may be effected with the above-mentioned polyhydric alcohols or their interesterification products with the above-mentioned drying oils which may be used in the form of their stand oils or after treatment with air, oxygen, sulphur, sulphur dioxide, anthraquinone or maleic anhydride, optionally together with oil-modified alkyd resins containing free hydroxyl groups. Specified isocyanates are phenyl-isocyanate, dichloro-phenyl-isocyanate, cyclohexyl-isocyanate, chlorophenylene-2,4-diisocyanate, toluylene-diisocyanate and 1,6-hexamethylene diisocyanate. The interesterification may be effected by heating in an inert atmosphere, e.g. of nitrogen, and the reaction with isocyanates at 130-200 DEG C., optionally in the presence of a solvent, e.g. white spirit and turpentine oil. Driers, e.g. cobalt, lead and manganese naphthenates may be added and the products used in the production of lacquers. In Example 2 a linseed oil modified glycerol phthalate resin is copolymerized with dicyclopentadiene in turpentine oil. Specification 711,611 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF15251A DE1007995B (en) | 1954-07-17 | 1954-07-17 | Process for the production of paint raw materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB794585A true GB794585A (en) | 1958-05-07 |
Family
ID=7087835
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2060155A Expired GB794585A (en) | 1954-07-17 | 1955-07-15 | Process for the manufacture of raw materials for lacquers |
Country Status (4)
Country | Link |
---|---|
DE (1) | DE1007995B (en) |
FR (1) | FR1141416A (en) |
GB (1) | GB794585A (en) |
NL (2) | NL90217C (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4178425A (en) * | 1976-07-07 | 1979-12-11 | Rohm And Haas Company | Polyurethane coating compositions containing unsaturated esters of glycol monodicyclopentenyl ethers |
US4180645A (en) | 1978-05-22 | 1979-12-25 | Rohm And Haas Company | Polyurethane coating compositions from dicyclopentenyl acrylate and/or methacrylate |
CN110527063A (en) * | 2019-07-09 | 2019-12-03 | 华伦纳路新材料有限公司 | Polyurethane-modified aqueous alkide resin of dicyclopentadiene and preparation method thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL241346A (en) * | 1958-07-23 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2503209A (en) * | 1948-01-30 | 1950-04-04 | American Cyanamid Co | Unsaturated alkyd reacted with unsaturated isocyanate |
-
0
- NL NL198117D patent/NL198117A/xx unknown
- NL NL90217D patent/NL90217C/xx active
-
1954
- 1954-07-17 DE DEF15251A patent/DE1007995B/en active Pending
-
1955
- 1955-06-21 FR FR1141416D patent/FR1141416A/en not_active Expired
- 1955-07-15 GB GB2060155A patent/GB794585A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4178425A (en) * | 1976-07-07 | 1979-12-11 | Rohm And Haas Company | Polyurethane coating compositions containing unsaturated esters of glycol monodicyclopentenyl ethers |
US4180645A (en) | 1978-05-22 | 1979-12-25 | Rohm And Haas Company | Polyurethane coating compositions from dicyclopentenyl acrylate and/or methacrylate |
CN110527063A (en) * | 2019-07-09 | 2019-12-03 | 华伦纳路新材料有限公司 | Polyurethane-modified aqueous alkide resin of dicyclopentadiene and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
FR1141416A (en) | 1957-09-02 |
NL90217C (en) | |
DE1007995B (en) | 1957-05-09 |
NL198117A (en) |
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