GB778026A - Improvements in or relating to the production of paint vehicle bases - Google Patents

Improvements in or relating to the production of paint vehicle bases

Info

Publication number
GB778026A
GB778026A GB26708/55A GB2670855A GB778026A GB 778026 A GB778026 A GB 778026A GB 26708/55 A GB26708/55 A GB 26708/55A GB 2670855 A GB2670855 A GB 2670855A GB 778026 A GB778026 A GB 778026A
Authority
GB
United Kingdom
Prior art keywords
acids
per cent
product
fatty
oil
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
GB26708/55A
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.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB778026A publication Critical patent/GB778026A/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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4292Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof together with monocarboxylic acids
    • 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
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Paints Or Removers (AREA)

Abstract

A paint vehicle is obtained by heating a glycidyl ether of a polyhydric phenol having at least one -OH group and from 1-2 epoxy groups per mol. with a fatty oil having an iodine number of 70-220 at 75 F. until a clear solution is obtained and then heating the product with 5-15 per cent by weight of a dicarboxylic acid or anhydride until incipient gelation occurs whereupon the product is thinned with a hydrocarbon thinner. The product obtained in the first stage may be heated with 3-20 per cent by weight of a monocarboxylic acid to reduce the iodine number by about 50 per cent. The glycidyl ether has preferably 3-10 -OH groups and 1.4-1.9 epoxy groups per mol. and the heating with the fatty oil is carried out in presence of an alcoholysis catalyst. The glycidyl ethers are prepared by reaction of epichlorhydrin with the usual dihydric phenols, e.g. resorcinol, hydroquinone and polynuclear phenols. A table is given of the Durrans' m.ps., hydroxyl, epoxy and esterification values of the products used. Fatty oils specified are soybean, linseed, corn, cottonseed, hemp, kapok, herring, perilla, poppy, pilchard, menhaden, mustard, peanut, rape, sardine, safflower, sesame, oiticia, walnut, tung, dehydrated castor and heat bodied linseed oils. Polyhydric alcohols, e.g. pentaerythritol, are preferably present during the action with the fatty oil. The monocarboxylic acids used have at least 6 C atoms, e.g. the free acid of the aforementioned oils; other suitable acids are caproic, caprylic, 2-ethylhexoic, lauric, palmitic, stearic, oleic, benzoic, p-ter.-butylbenzoic, naphthenic acids, cinnamic, hydrogenated rosin. The dicarboxylic acids specified for the second stage are malonic, succinic, sebacic, glutaric, azelaic, sebacic, maleic, phthalic, tetrahydrophthalic, hexahydrophthalic, diglycolic, dimerized drying oil fatty acids, dimerized rosin, Diels-Alder adducts of maleic anhydride with diolefines, e.g. terpenes and cyclopentadiene, petrex acids. In examples (1) a polyether obtained from epichlorhydrin and bisphenol is reacted at 555 DEG F. with a soybean oil having an iodine no. of 130. The product is further reacted with soybean acids and adipic acids until gelation starts whereupon a solvent consisting of 75 per cent paraffin and 25 per cent naphthenes is added. The base obtained is used to make up pigment mixtures of (a) titanium dioxide calcium carbonate and aluminium stearate; (b) red iron oxide, black iron oxide, calcium carbonate and aluminium stearate. Specification 737,272 is referred to.
GB26708/55A 1954-09-20 1954-09-19 Improvements in or relating to the production of paint vehicle bases Expired GB778026A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US338304XA 1954-09-20 1954-09-20

Publications (1)

Publication Number Publication Date
GB778026A true GB778026A (en) 1957-07-03

Family

ID=21872696

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26708/55A Expired GB778026A (en) 1954-09-20 1954-09-19 Improvements in or relating to the production of paint vehicle bases

Country Status (6)

Country Link
BE (1) BE541405A (en)
CH (1) CH338304A (en)
DE (1) DE1043555B (en)
FR (1) FR1146564A (en)
GB (1) GB778026A (en)
NL (2) NL99271C (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL128254C (en) * 1963-04-16
EP0009526A1 (en) * 1978-10-10 1980-04-16 Mobil Oil Corporation Water-solubilizable epoxy resin and coating composition comprising the resin for metal food contact surfaces

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE514996A (en) * 1951-10-22

Also Published As

Publication number Publication date
FR1146564A (en) 1957-11-13
CH338304A (en) 1959-05-15
NL99271C (en)
DE1043555B (en) 1958-11-13
BE541405A (en)
NL200557A (en)

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