GB1088374A - Water dilutable surface coating alkyd resins - Google Patents

Water dilutable surface coating alkyd resins

Info

Publication number
GB1088374A
GB1088374A GB5058663A GB5058663A GB1088374A GB 1088374 A GB1088374 A GB 1088374A GB 5058663 A GB5058663 A GB 5058663A GB 5058663 A GB5058663 A GB 5058663A GB 1088374 A GB1088374 A GB 1088374A
Authority
GB
United Kingdom
Prior art keywords
diol
water
acids
acid
residues
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
GB5058663A
Inventor
Parry Williams
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co 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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB5058663A priority Critical patent/GB1088374A/en
Priority to FR999151A priority patent/FR1417792A/en
Publication of GB1088374A publication Critical patent/GB1088374A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08G63/66Polyesters containing oxygen in the form of ether groups
    • C08G63/668Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds

Abstract

Water-dilutable alkyd resins have a backbone comprising residues of polyols, of which at least 90% by weight are residues of hindered diols, and polycarboxylic acids having at least three carboxyl groups per molecule, the resin also containing residues containing b g -ethylenically unsaturated ether groups, and sufficient carboxyl groups to render the resin water dilutable. The hindered diols have at least three carbon atoms, a carbon atom next to each carbon atom carrying the hydroxyl groups being fully substituted by alkyl, aryl or aralkyl groups, preferably C1- 4 alkyl groups, and may be e.g. neopentyl glycol, 2-methyl-2-ethyl-propane-1,3-diol, 2,2 - diethylpropane - 1,3 - diol, 2,2 - dimethylpentane-1,3-diol 2,2-dimethylbutane-1,3 - diol and 2,2,4 - trimethylpentane - 1,3-diol. Suitable polycarboxylic acids are trimellitic, trimesic, hemimellitic, pyromellitic, tricarballylic and camphoronic acids. The unsaturated groups may be derived from mono- or polyhydric alcohols containing at least one b ,g -ethylenically unsaturated ether group, e.g. the monoallyl and diallyl ethers of glycerol, trimethylol ethane and trimethylol propane, and the monoallyl, diallyl and triallyl ethers of pentaerythritol, and the corresponding methallyl compounds. The resins have acid values of at least 30, preferably 50 to 100. The polycarboxylic acids and hindered diols may be replaced by up to 50 mol. per cent of mono- and dibasic acids, e.g. phthalic or maleic acid, and up to 10 wt. per cent of other polyols, respectively. The resin may also contain residues of saturated or unsaturated fatty acids, e.g. dehydrated castor oil acids. It may be prepared by partially esterifying the polycarboxylic acid with the unsaturated ether alcohol, esterifying the resulting ester having at least two free carboxyl groups per molecule, with the hindered diol, and further esterifying the product with more polycarboxylic acid. Fatty acid residues may be introduced at the same time as the hindered diol The polycarboxylic acids are preferably used as anhydrides. The resin is dissolved or dispersed in water or water containing a water-miscible organic solvent, e.g. ethanol, propanol or butanol, or the methyl, ethyl or butyl mono-ethers of ethylene glycol, in the presence of a base, which is preferably volatile, e.g. ammonium hydroxide or a volatile amine, e.g. triethylamine, to give a solution or emulsion which may be diluted with water. In examples, 1 mol. of trimellitic anhydride is reacted with 1 mol. of trimethylol propane diallyl ether to an acid value of 276, then esterified with 2 mols. of neopentyl glycol and 0.75 mols. of dehydrated castor oil fatty acids to an acid value of 5-10, and finally reacted with 0.5 or 0.54 mols. of trimellitic anhydride to an acid value of 64. The resins were dissolved in water containing triethylamine and a cobalt drier, and used to make surface coatings.
GB5058663A 1963-12-21 1963-12-21 Water dilutable surface coating alkyd resins Expired GB1088374A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB5058663A GB1088374A (en) 1963-12-21 1963-12-21 Water dilutable surface coating alkyd resins
FR999151A FR1417792A (en) 1963-12-21 1964-12-18 Alkyd resins which can be diluted with water, suitable for use as surface coatings

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5058663A GB1088374A (en) 1963-12-21 1963-12-21 Water dilutable surface coating alkyd resins

Publications (1)

Publication Number Publication Date
GB1088374A true GB1088374A (en) 1967-10-25

Family

ID=10456506

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5058663A Expired GB1088374A (en) 1963-12-21 1963-12-21 Water dilutable surface coating alkyd resins

Country Status (1)

Country Link
GB (1) GB1088374A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4215179A (en) 1979-03-30 1980-07-29 Rohm And Haas Company Coating concrete with latex polymers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4215179A (en) 1979-03-30 1980-07-29 Rohm And Haas Company Coating concrete with latex polymers

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