GB1082303A - New polyesters - Google Patents
New polyestersInfo
- Publication number
- GB1082303A GB1082303A GB1121464A GB1121464A GB1082303A GB 1082303 A GB1082303 A GB 1082303A GB 1121464 A GB1121464 A GB 1121464A GB 1121464 A GB1121464 A GB 1121464A GB 1082303 A GB1082303 A GB 1082303A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mixture
- alcohols
- acids
- acid
- ethylene glycol
- 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
- C09D161/00—Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
- C09D161/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/123—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/127—Acids containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Polyesters are prepared by heating one or more benzene-o-dicarboxylic acids with one or more monohydric alcohols of at least 5 C atoms and a mixture of polyhydric alcohols such that more than 2/3 of the hydroxyl groups therein are primary, and optionally one or more monobasic carboxylic acids, provided that at most 30 wt. per cent of the reagents contributing the carbonyl portion of the ester groups are acids whose ethyl esters have an alkaline hydrolysis constant in water at 25 DEG C. greater than 10-2 litre/mole/sec. The heating is preferably continued until the product has an acid value below 50, the proportions of reagents being such that the hydroxy value is then 50-250. The preferred major acid component is phthalic acid with a -substituted alkanoic acids, e.g. 2-methylnonanoic acid, or benzoic acid as monocarboxylic acids; suitable minor acid components (i.e. those limited to 30 wt. per cent) are castor, dehydrated castor, perilla, coconut, cottonseed, train, soybean and tall oil fatty acids, stearin, succinic, adipic, maleic, acrylic, isophthalic and trimellitic acids. Suitable polyols are ethylene-, diethylene-, propylene- and polypropylene-glycols, butane-1:4-, pentane-1:5-, butene-1:3- and 2-methylpentane-2:4-diols, glycerol, hexane-1:2:6-triol, trimethylol propane, trimethylolethane and pentaerythritol dipentaerythritol and sorbitol. Monohydric alcohols that may be used include amyl, cyclohexyl, decyl, lauryl and stearyl alcohols and oxo or natural oil alcohols. Compositions may include a polyester of the invention, a curable aminoplast resin and a volatile organic solvent. Suitable aminoplasts are methylol derivatives of urea, ethyleneurea, uron, acetoguanamine, benzoguanomine, melamine and ethers of these with e.g. ethanol, butanol, butenol, allyl alcohol, ethylene glycol, glycerol, and ethylene glycol monoethyl ether. Preferred proportions of polyester: aminoplast lie in the range 9:1-1:1. In examples polyesters are prepared from phthalic anhydride and a mixture of trimethylolpropane and hexane-1:2:6-triol or of pentaerythritol and ethylene glycol, and isodecyl alcohol or a synthetic mixture of alcohols. They are mixed with a methylated or butylated methylol melamine resin, rutile TiO2 and a xylene/n-butanol mixture, to give a varnish.ALSO:Tinplate or steel is coated with a varnish comprising a volatile organic solvent, an aminoplast resin, and a polyester derived from a benzene-o-dicarboxylic acid, a mono hydric alcohol of 5 or more C atoms, and a mixture of polyols (see Division C3). In Examples the polyesters derived from phthalic anhydride, isodecanol or an 'oxo' mixture of alcohols, and a trimethylolpropane/hexanetriol or penta erythritol/ethylene glycol mixture; they are mixed with butylated or methylated methylol melamine and TiO2 in xylene/butanol mixture.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1121464A GB1082303A (en) | 1964-03-17 | 1964-03-17 | New polyesters |
NL6503381A NL6503381A (en) | 1964-03-17 | 1965-03-17 | |
FR9631A FR1451272A (en) | 1964-03-17 | 1965-03-17 | New polyesters and their manufacturing process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1121464A GB1082303A (en) | 1964-03-17 | 1964-03-17 | New polyesters |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1082303A true GB1082303A (en) | 1967-09-06 |
Family
ID=9982108
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1121464A Expired GB1082303A (en) | 1964-03-17 | 1964-03-17 | New polyesters |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB1082303A (en) |
NL (1) | NL6503381A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1926035A1 (en) * | 1969-05-22 | 1970-11-26 | Reichhold Albert Chemie Ag | Heat-curable binder for the production of molded articles |
US4042547A (en) * | 1973-04-18 | 1977-08-16 | Bayer Aktiengesellschaft | Environmentally harmless stoving lacquer systems based on alkyd resins containing condensed monohydric alcohols |
-
1964
- 1964-03-17 GB GB1121464A patent/GB1082303A/en not_active Expired
-
1965
- 1965-03-17 NL NL6503381A patent/NL6503381A/xx unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1926035A1 (en) * | 1969-05-22 | 1970-11-26 | Reichhold Albert Chemie Ag | Heat-curable binder for the production of molded articles |
US4042547A (en) * | 1973-04-18 | 1977-08-16 | Bayer Aktiengesellschaft | Environmentally harmless stoving lacquer systems based on alkyd resins containing condensed monohydric alcohols |
Also Published As
Publication number | Publication date |
---|---|
NL6503381A (en) | 1965-09-20 |
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