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GB532532A - Improvements in or relating to heat convertible synthetic resin compositions - Google Patents

Improvements in or relating to heat convertible synthetic resin compositions

Info

Publication number
GB532532A
GB532532A GB21466/39A GB2146639A GB532532A GB 532532 A GB532532 A GB 532532A GB 21466/39 A GB21466/39 A GB 21466/39A GB 2146639 A GB2146639 A GB 2146639A GB 532532 A GB532532 A GB 532532A
Authority
GB
United Kingdom
Prior art keywords
urea
resin
alkyd
per cent
acids
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
GB21466/39A
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 GB532532A publication Critical patent/GB532532A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08L61/22Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
    • C08L61/24Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with urea or thiourea
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/08Polyesters modified with higher fatty oils or their acids, or with resins or resin acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

532,532. Synthetic resin compositions. INTERCHEMICAL CORPORATION. July 24, 1939, Nos. 21466 and 21467. Convention dates, April 12 and July 11. [Class 2 (iii)] A heat-convertible synthetic resin composition which does not discolour at high temperatures comprises a urea-formaldehyde resin soluble in organic solvents and a heat-convertible alkyd resin consisting of the reaction product of a polyhydric alcohol, phthalic acid and one or more of lauric, myristic and palmitic acids, which acids are substantially free from unsaturated fatty compounds and containing less than 10 per cent. of other saturated acid. The fatty acid constitutes 20-60 per cent. of the alkyd resin and the ratio of alkyd to urea resin is between 1:5 and 5:1. Phthalic acid may be replaced by other dibasic acids up to a few per cent. To avoid discoloration, the urea resin should be prepared from formaldehyde and urea or urea derivatives other than thiourea and other discolouring derivatives, and the finished composition should be substantially free from non-volatile fatty acid compounds. Examples are given of the preparation of (1) a urea resin by heating together formaldehyde and phosphoric acid, adding urea in stages at 60-65‹C., then raising the temperature to 85-90‹C. and, after a time adding n-butanol and mildly refluxing at 90-95‹C. and finally distilling off water and butanol and adjusting the solution to a 50 per cent. non-volatile content; (2)-(6) alkyd resins from phthalic anhydride, glycerine and lauric (2 and 3), myristic (4 and 5) and palmitic (6) acids by heating to 450‹F. in an aluminium kettle in an atmosphere of carbon dioxide ; (7) a coating composition by mixing the urea resin solution of (1) with a xylol solution of (2) and titanium oxide, which composition may be sprayed on metal and baked for 30 minutes at 250 F. or 10 minutes at 350 F., and (8) and (9) moulding compositions by blending the urea resin, preferably with some of the solvent removed, with the solid alkyd resin on a two-roller mill to produce a powder which can be moulded at 350‹F. under a pressure of 2,000 lb. per sq. inch for 10 minutes.
GB21466/39A 1939-04-12 1939-07-24 Improvements in or relating to heat convertible synthetic resin compositions Expired GB532532A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US532532XA 1939-04-12 1939-04-12

Publications (1)

Publication Number Publication Date
GB532532A true GB532532A (en) 1941-01-27

Family

ID=21982925

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21466/39A Expired GB532532A (en) 1939-04-12 1939-07-24 Improvements in or relating to heat convertible synthetic resin compositions

Country Status (1)

Country Link
GB (1) GB532532A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2560319A (en) * 1945-01-04 1951-07-10 American Cyanamid Co Heat-stable plasticized aminotriazine resin compositions
US2663694A (en) * 1949-09-01 1953-12-22 Glidden Co Alkyd modified siloxane coating compositions

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2560319A (en) * 1945-01-04 1951-07-10 American Cyanamid Co Heat-stable plasticized aminotriazine resin compositions
US2663694A (en) * 1949-09-01 1953-12-22 Glidden Co Alkyd modified siloxane coating compositions

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