GB532332A - Improvements in or relating to alkyd resins and coating compositions prepared therefrom - Google Patents

Improvements in or relating to alkyd resins and coating compositions prepared therefrom

Info

Publication number
GB532332A
GB532332A GB21470/39A GB2147039A GB532332A GB 532332 A GB532332 A GB 532332A GB 21470/39 A GB21470/39 A GB 21470/39A GB 2147039 A GB2147039 A GB 2147039A GB 532332 A GB532332 A GB 532332A
Authority
GB
United Kingdom
Prior art keywords
acids
acid
glycerol
lauric
per cent
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
GB21470/39A
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.)
Interchemical Corp
Original Assignee
Interchemical Corp
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 Interchemical Corp filed Critical Interchemical Corp
Publication of GB532332A publication Critical patent/GB532332A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/08Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Paints Or Removers (AREA)

Abstract

532,332. Synthetic resin compositions containing wetting and luminescent agent. INTERCHEMICAL CORPORATION. July 24, 1939, Nos. 21470 and 21471. Convention dates, April 12 and July 11. [Class 2 (iii)] Resins are prepared by heating together a polyhydric alcohol, e.g. glycol or glycerol, phthalic acid, and one or more of lauric, myristic and palmitic acids substantially free from unsaturated fatty acid compounds and containing less than 10 per cent. of other saturated acids. A few per cent. of phthalic acid may be replaced by other dibasic acids. The fatty acid may constitute 20 to 60 per cent. of the reaction mix. The products are soluble in hydrocarbons, e.g. toluene, xylene, solvent naphtha, or hydrogenated petroleum naphtha, to produce coating compositions, which may be pigmented, e.g. with titanium dioxide, and may be blended with cellulosic lacquers. In examples : glycerol, phthalic anhydride, and lauric, myristic, or palmitic acids, or coconut oil fatty acids from which unsaturated bodies have been removed, are heated in an atmosphere of carbon dioxide ; or glycerol, phthalic anhydride fumaric acid, and lauric acid are similarly reacted.
GB21470/39A 1939-04-12 1939-07-24 Improvements in or relating to alkyd resins and coating compositions prepared therefrom Expired GB532332A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US858344XA 1939-04-12 1939-04-12
US532332XA 1939-04-12 1939-04-12

Publications (1)

Publication Number Publication Date
GB532332A true GB532332A (en) 1941-01-22

Family

ID=26731607

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21470/39A Expired GB532332A (en) 1939-04-12 1939-07-24 Improvements in or relating to alkyd resins and coating compositions prepared therefrom

Country Status (2)

Country Link
FR (1) FR858344A (en)
GB (1) GB532332A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108395524A (en) * 2018-02-01 2018-08-14 新纶科技(常州)有限公司 A kind of saturated fatty acid alkyd resin intermediate and its synthetic method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108395524A (en) * 2018-02-01 2018-08-14 新纶科技(常州)有限公司 A kind of saturated fatty acid alkyd resin intermediate and its synthetic method

Also Published As

Publication number Publication date
FR858344A (en) 1940-11-22

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