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GB1082303A - New polyesters - Google Patents

New polyesters

Info

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
Application number
GB1121464A
Inventor
John Leslie Hugh Allan
Alan Ferguson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1121464A priority Critical patent/GB1082303A/en
Priority to NL6503381A priority patent/NL6503381A/xx
Priority to FR9631A priority patent/FR1451272A/en
Publication of GB1082303A publication Critical patent/GB1082303A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D161/00Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
    • C09D161/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/123Polyesters 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
    • C08G63/127Acids containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions 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.
GB1121464A 1964-03-17 1964-03-17 New polyesters Expired GB1082303A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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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