GB1022252A - Improvements in and relating to resins - Google Patents

Improvements in and relating to resins

Info

Publication number
GB1022252A
GB1022252A GB1630362A GB1630362A GB1022252A GB 1022252 A GB1022252 A GB 1022252A GB 1630362 A GB1630362 A GB 1630362A GB 1630362 A GB1630362 A GB 1630362A GB 1022252 A GB1022252 A GB 1022252A
Authority
GB
United Kingdom
Prior art keywords
product
reacting
give
phenol
drying
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
GB1630362A
Inventor
John Liberty Smith
Reginald Davis Singer
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.)
Dunlop Rubber Co Ltd
Original Assignee
Dunlop Rubber 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 Dunlop Rubber Co Ltd filed Critical Dunlop Rubber Co Ltd
Priority to GB1630362A priority Critical patent/GB1022252A/en
Publication of GB1022252A publication Critical patent/GB1022252A/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
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/28Chemically modified polycondensates
    • C08G8/32Chemically modified polycondensates by organic acids or derivatives thereof, e.g. fatty oils

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

Alkali-soluble resins suitable for coating compositions are obtained by (a) reacting a drying or semi-drying oil with sufficient maleic anhydride or maleic, fumaric or itaconic acid to give a product soluble in aqueous alkali; (b) reacting the product with a phenol; and (c) reacting the product of (b) with an aldehyde. Specified reactants are:-drying oils cottonseed, soybean, corn, oiticia, tung, linseed and pirella oils; phenols phenol, cresol, resorcinol, catechol and alkylphenols; aldehydes formaldeydehyde and acetaldehyde. Each step is preferably conducted in an inert atmosphere. A suitable catalyst for step (b) is oleum. In the specific example the catalyst for step (c) is ammonia. The final product may be dissolved or dispersed in aqueous ammonia or a volatile organic base such as methylamine or morpholine, optionally with filler and pigments to give a coating composition. In the specific example a resin is prepared from tung oil, maleic anhydride, phenol and formaldehyde and a solution thereof in diethylaminoethanol is mixed with a dispersion of red iron oxide and is painted on to steel panels to give after heating at 160 DEG C. for 30 minutes, a hard flexible coating resistant to hot water and salt water spray.ALSO:Steel panels are coated with a composition containing an alkali-soluble resin obtained by (a) reacting a drying or semi-drying oil with sufficient maleic anhydride or maleic, fumaric or itaconic acid to give a product soluble in aqueous alkali; (b) reacting the product with a phenol; and (c) reacting the product of (b) with an aldehyde. Specified reactants are: drying oils cottonseed, soybean, corn, oiticia, tung, linseed and pirella oils; phenols phenol, cresol, resorcinol, catechol and alkylphenols; aldehydes formaldehyde and acetaldehyde. Each step is preferably conducted in an inert atmosphere. A suitable catalyst for step (b) is oleum. In the specific example the catalyst for step (c) is ammonia. The final product may be dissolved or dispersed in aqueous ammonia or a volatile organic base such as methylamine or morpholine, optionally with filler and pigments to give a coating composition. In the specific example a resin is prepared from tung oil, maleic anhydride, phenol and formaldehyde and a solution thereof in diethylamino-ethanol is mixed with a dispersion of red iron oxide and is painted on to steel panels to give after heating at 160 DEG C. for 30 minutes, a hard flexible coating resistant to hot water and salt water spray.
GB1630362A 1962-04-28 1962-04-28 Improvements in and relating to resins Expired GB1022252A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1630362A GB1022252A (en) 1962-04-28 1962-04-28 Improvements in and relating to resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1630362A GB1022252A (en) 1962-04-28 1962-04-28 Improvements in and relating to resins

Publications (1)

Publication Number Publication Date
GB1022252A true GB1022252A (en) 1966-03-09

Family

ID=10074873

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1630362A Expired GB1022252A (en) 1962-04-28 1962-04-28 Improvements in and relating to resins

Country Status (1)

Country Link
GB (1) GB1022252A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102225922A (en) * 2011-04-14 2011-10-26 中山大学 Preparation method of urethane modified tung oil vinylite

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102225922A (en) * 2011-04-14 2011-10-26 中山大学 Preparation method of urethane modified tung oil vinylite

Similar Documents

Publication Publication Date Title
GB1016957A (en) Coating composition particularly for electrodeposition
DE1520918B2 (en) METHOD OF MANUFACTURING EPOXY POLYADDUCTS
GB1088198A (en) Gravure ink for paper
DE943494C (en) Process for the manufacture of curable polyesters
GB1022252A (en) Improvements in and relating to resins
GB609750A (en) Improvements in or relating to the manufacture of interpolymers of styrene with polyhydric alcoholic mixed esters and of coating compositions obtained therefrom
CN104946016B (en) A kind of raw lacquer ink solidified for digital spray printing and UV and its modulator approach
GB657867A (en) Vinyl resin coating
US3529993A (en) Polyanhydride-polyamine coated surface and method of coating
GB943155A (en) Improvements in and relating to synthetic resinous products for surface coatings
GB1059912A (en) Water soluble paint compositions
US2027337A (en) Manufacture of resins
US2060625A (en) Process of preparing self-hardening compositions and products obtainable therbey
US2283353A (en) Varnish composition
US2871208A (en) Oil soluble butenylphenol formaldehyde resins
US4025473A (en) Process for producing water-dilutable coating compositions
GB1146694A (en) Water-dilutable coating compositions and lacquer binders
US3188235A (en) China-wood oil and amine resin compositions
GB1207794A (en) Water-thinnable condensation products and their use as paint binders
GB345845A (en) Improvements in or relating to varnishes and lacquers
GB1019658A (en) Method for the electrical deposition of synthetic resin coatings
GB953761A (en) Thermosettable coating formulations and coated articles
GB337192A (en) Improvements in or relating to the application of varnishes, lacs or like coatings to metal surfaces
DE2523878C2 (en) Aqueous coating agent made from phenolic resins and polyester adducts
JPH0621269B2 (en) Resin composition for paint