GB1006602A - Improvements in and relating to the production of resins - Google Patents

Improvements in and relating to the production of resins

Info

Publication number
GB1006602A
GB1006602A GB821861A GB821861A GB1006602A GB 1006602 A GB1006602 A GB 1006602A GB 821861 A GB821861 A GB 821861A GB 821861 A GB821861 A GB 821861A GB 1006602 A GB1006602 A GB 1006602A
Authority
GB
United Kingdom
Prior art keywords
polyol
vinyl
acid
glycerol
styrene
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
GB821861A
Inventor
David Vernon Hudson Jones
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.)
Coates Brothers and Co Ltd
Original Assignee
Coates Brothers and 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 Coates Brothers and Co Ltd filed Critical Coates Brothers and Co Ltd
Priority to GB821861A priority Critical patent/GB1006602A/en
Publication of GB1006602A publication Critical patent/GB1006602A/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)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

A method of making drying oil modified alkyd resins comprises subjecting a drying oil to acidolysis with a polybasic acid, and reacting the acidolysis product with a polyol and a vinylidene compound. The acidolysis product may be reacted first with the vinyl compound and then with the polyol, or may be reacted simultaneously with the vinyl compound and polyol. When the polybasic acid comprises o-phthalic acid the acidolysis product is preferably treated first with a substantial portion of the polyol, and then with the remainder of the polyol and the vinyl compound. The drying oil may be linseed, soya or dehydrated castor oil. The polybasic acid may be a phthalic acid or phthalic anhydride, optionally with up to 10% of fumaric or maleic acid. The polyol may be glycerol, pentaerythritol or trimethylol propane. Specified vinyl idene compounds are styrene, vinyl toluene, acrylic and methacrylic esters such as methyl methacrylate, and mixtures of vinyl toluene with acrylonitrile. Reaction with the polyol and vinyl compound may be effected under reflux using e.g. styrene or an inert solvent such as xylene as entrainment solvent. Reaction with the vinyl compound may be effected in the presence of initiators, e.g. benzoyl peroxide and di-t.-butyl peroxide, and chain transfer agents, such as mercaptans and dipentene. Examples describe the preparation of reaction products from linseed oil, isophthalic acid and vinyl toluene with (I) pentaerythritol and (II) glycerol; and a mixture of soya bean oil and dehydrated castor oil with phthalic anhydride and glycerol and (III) styrene and (IV) styrene and acrylonitrile, and with (V) isophthalic acid, glycerol and methyl methacrylate.
GB821861A 1961-03-07 1961-03-07 Improvements in and relating to the production of resins Expired GB1006602A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB821861A GB1006602A (en) 1961-03-07 1961-03-07 Improvements in and relating to the production of resins

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB821861A GB1006602A (en) 1961-03-07 1961-03-07 Improvements in and relating to the production of resins

Publications (1)

Publication Number Publication Date
GB1006602A true GB1006602A (en) 1965-10-06

Family

ID=9848201

Family Applications (1)

Application Number Title Priority Date Filing Date
GB821861A Expired GB1006602A (en) 1961-03-07 1961-03-07 Improvements in and relating to the production of resins

Country Status (1)

Country Link
GB (1) GB1006602A (en)

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