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GB619975A - Improvements in or relating to the production of oil-modified alkyd resins and to improved coating compositions prepared therefrom - Google Patents

Improvements in or relating to the production of oil-modified alkyd resins and to improved coating compositions prepared therefrom

Info

Publication number
GB619975A
GB619975A GB2231446A GB2231446A GB619975A GB 619975 A GB619975 A GB 619975A GB 2231446 A GB2231446 A GB 2231446A GB 2231446 A GB2231446 A GB 2231446A GB 619975 A GB619975 A GB 619975A
Authority
GB
United Kingdom
Prior art keywords
anhydride
glycerol
acid
added
heating
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
GB2231446A
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.)
British Resin Products Ltd
Original Assignee
British Resin Products 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 British Resin Products Ltd filed Critical British Resin Products Ltd
Priority to GB2231446A priority Critical patent/GB619975A/en
Publication of GB619975A publication Critical patent/GB619975A/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
    • C08G63/02Polyesters 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
    • C08G63/46Polyesters chemically modified by esterification
    • C08G63/48Polyesters chemically modified by esterification by unsaturated higher fatty oils or their acids; by resin acids

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)
  • Polyurethanes Or Polyureas (AREA)
  • Paints Or Removers (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

Oil-modified alkyd resins are prepared by heating a mixture of castor oil, a polyhydric alcohol and a polybasic acid or anhydride thereof at a temperature between 260 DEG and 270 DEG C. until the initial decrease in viscosity of the reaction mixture has substantially ceased, and, before there is any substantial increase in viscosity adding a sufficient quantity of polyhydric alcohol and/or polybasic acid or anhydride thereof at such a temperature as to reduce the temperature of the reaction mixture to a value not exceeding 230 DEG C., and continuing to react the added polyhydric alcohol and added polybasic acid or anhydride thereof at a temperature between 160 DEG and 230 DEG C. and adding any further polyhydric alcohol and/or polybasic acid or anhydride which may be necessary to produce a reaction product, the oil content of which does not exceed 50 per cent thereof and which contains a small amount of free polyhydric alcohol. Cooling means may be provided to remove the excess heat of the reaction vessel. Preferably, the initial reaction mixture contains 5-75 per cent excess of glycerol over the equivalent amount and contains 40-95 per cent of oil. Any further additions of polyhydric alcohol are preferably made before the addition of further polybasic-acid. Suitable alcohols are glycerol, pentaery, thritol, ethylene glycol, trimethylol propane mannitol, sorbitol and butyne-diol, and suitable acids are phthalic acid and anhydride, tetrahydrophthalic acid, tetrachlorophthalic anhydride, methylene di-salicylic acid, maleic, fumaric and citric acids, and maleic and fumaric acid adducts with terpenes and cyclo-olefines. In examples, castor oil, glycerol and phthalic anhydride are heated at 260-270 DEG C., and when the minimum viscosity is passed sufficient glycerol is added to reduce the temperature to 230 DEG C. Further phthalic anhydride is added, followed by further heating, firstly at 230 DEG C. and then at 180 DEG C.; (2) the procedure of (1) is followed, but a further addition of phthalic anhydride and glycerol is made whilst heating at 180 DEG C.; (3) castor oil, phthalic anhydride and glycerol are heated at 260-270 DEG C. and pentaerythritol added when the minimum viscosity is passed to reduce the temperature to 230 DEG C. Phthalic acid is added and heating continued at 220 DEG C.; (4) sorbitol replaces the pentaerythritol of (3). The products dissolved in xylene are p suitable as varnishes, and cobalt linoleate or naphthenate driers may be added. Specifications 431,495 and 474,620 are referred to. A sample has been furnished under Sect. 2 (5) of a product obtained by heating castor oil glycerol and phthalic anhydride, and when the minimum viscosity is reached adding more glycerol and phthalic anhydride and heating at 220 DEG C., then adding butyne diol and heating at 210 DEG C. The product at 200 DEG C. is dissolved in xylene.
GB2231446A 1946-07-26 1946-07-26 Improvements in or relating to the production of oil-modified alkyd resins and to improved coating compositions prepared therefrom Expired GB619975A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2231446A GB619975A (en) 1946-07-26 1946-07-26 Improvements in or relating to the production of oil-modified alkyd resins and to improved coating compositions prepared therefrom

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2231446A GB619975A (en) 1946-07-26 1946-07-26 Improvements in or relating to the production of oil-modified alkyd resins and to improved coating compositions prepared therefrom

Publications (1)

Publication Number Publication Date
GB619975A true GB619975A (en) 1949-03-17

Family

ID=10177380

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2231446A Expired GB619975A (en) 1946-07-26 1946-07-26 Improvements in or relating to the production of oil-modified alkyd resins and to improved coating compositions prepared therefrom

Country Status (1)

Country Link
GB (1) GB619975A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010023532A1 (en) * 2008-08-26 2010-03-04 Ennatura Technology Ventures (P) Ltd. Water reducible alkyd resins

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010023532A1 (en) * 2008-08-26 2010-03-04 Ennatura Technology Ventures (P) Ltd. Water reducible alkyd resins

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