GB569525A - Improvements in and relating to synthetic resins - Google Patents

Improvements in and relating to synthetic resins

Info

Publication number
GB569525A
GB569525A GB13274/42A GB1327442A GB569525A GB 569525 A GB569525 A GB 569525A GB 13274/42 A GB13274/42 A GB 13274/42A GB 1327442 A GB1327442 A GB 1327442A GB 569525 A GB569525 A GB 569525A
Authority
GB
United Kingdom
Prior art keywords
acrylic
furyl
acid
glycerol
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
GB13274/42A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of GB569525A publication Critical patent/GB569525A/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

Landscapes

  • 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)
  • Polyesters Or Polycarbonates (AREA)

Abstract

Alkyd resins are modified with a b -furylacrylic acid or an esterifiable derivative thereof. They may be further modified with fatty oils, particularly drying and semi-drying oils such as linseed and soya oils. The products dry quickly, to very hard films. A preferred method is to heat a drying oil with a polyhydric alcohol in the presence of an alcoholysis catalyst to form a partial polyhydric alcohol ester, and then to esterify this partial ester with a polybasic acid and a b -furylacrylic acid. The preferred b -furylacrylic acid is b -(2-furyl) acrylic acid, but other specified acids are a -methyl-b -(2-furyl)acrylic, a -cyano-b -(2-furyl) acrylic, a : b - di - (2 - furyl)acrylic, a -phenyl-b -(2 - furyl)acrylic, a : b - dimethyl - b - (2 - furyl) acrylic, b -cyclohexyl - b - (2 - furyl)acrylic, b -(3-furyl)acrylic, b -[2 - (5-methylfuryl)]acrylic, and b -[2- (5 - chlorofuryl)]acrylic acids. According to examples: (1) soya oil, glycerol and litharge are heated together, and phthalic anhydride and xylene are then added, and heating contined. b -(2-Furyl)acrylic acid and further glycerol are added, and heating continued. The resin is thinned with mineral spirits and a cobalt drier is added. The solution dries quickly to a hard film; (2) linseed oil, glycerol and sodium hydroxide are heated together under a carbon dioxide blanket, and the product is mixed with more glycerol, phthalic anhydride, b -(2-furyl)acrylic acid and xylene, and heated further. On the addition of a drier, a fast- and hard-drying clear coating composition is obtained; (5) soya oil, linseed oil, glycerol, mineral spirits and an aqueous solution of sodium hydroxide are heated together. Phthalic anhydride, maleic anhydride and b -(2-furyl)acrylic acid are then added, and heating continued; (9) a resin prepared from coconut oil, glycerol, phthalic anhydride and b -(2-furyl)acrylic acid, is mixed with nitrocellulose, ethyl acetate, butanol, butyl acetate and toluene, to produce a lacquer drying to hard but flexible films. Other examples are given, in which dehydrated castor oil, coconut oil, pentaerythritol, and adipic acid are specified starting materials. Many alternative polyhydric alcohols and polycarboxylic acids are specified. Other modifying agents which can be used include chinawood, cottonseed, oiticica, perilla, sunflower seed and corn oils; butyric, stearic, acrylic, oleic, glycollic, lactic, chloroacetic, benzoic, salicylic and rosin acids; butyl, n-dodecyl, allyl, benzyl and cyclohexyl alcohols; and the various synthetic oils which are described in Specification 569,404. Coating compositions prepared from the resins of this invention may comprise driers, pigments such as barytes and titanium oxide, and solvents such as mineral spirits, toluene, butanol, butyl acetate, ethyl acetate and b -ethoxyethanol.
GB13274/42A 1941-09-19 1942-09-21 Improvements in and relating to synthetic resins Expired GB569525A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US569525XA 1941-09-19 1941-09-19

Publications (1)

Publication Number Publication Date
GB569525A true GB569525A (en) 1945-05-29

Family

ID=22007591

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13274/42A Expired GB569525A (en) 1941-09-19 1942-09-21 Improvements in and relating to synthetic resins

Country Status (1)

Country Link
GB (1) GB569525A (en)

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