GB592400A - Improvements in and relating to the manufacture of synthetic resins - Google Patents

Improvements in and relating to the manufacture of synthetic resins

Info

Publication number
GB592400A
GB592400A GB579/44A GB57944A GB592400A GB 592400 A GB592400 A GB 592400A GB 579/44 A GB579/44 A GB 579/44A GB 57944 A GB57944 A GB 57944A GB 592400 A GB592400 A GB 592400A
Authority
GB
United Kingdom
Prior art keywords
castor oil
heating
mols
acid
pyridine
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
GB579/44A
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 Thomson Houston Co Ltd
Original Assignee
British Thomson Houston 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 British Thomson Houston Co Ltd filed Critical British Thomson Houston Co Ltd
Publication of GB592400A publication Critical patent/GB592400A/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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

1-3 mols. of an unsaturated dicarboxylic acid are reacted with 1 mol. of castor oil to form an ester in which half the carboxyl group of the acid are unesterified, and the unesterified carboxyl groups are removed by heating with pyridine, quinoline, nicotine, or piperidine to yield a viscous resin which is polymerized to a solid resin with the aid of a peroxide catalyst. The decarboxylated product may be copolymerized with styrene or a higher methacrylic ester, e.g. butyl methacrylate. A mixture of the decarboxylated product with castor oil with or without butyl or another methacrylate is also useful. Suitable dicarboxylic acids are maleic, fumaric or itaconic. The compositions are suitable for casting, as filling compounds, or particularly when mixed with siccatives, as coating, impregnating or insulating compositions, with or without fillers such as wood flour, asbestos, glass fibre, sand or paper. In the examples: (1) 1.6 mols. of maleic anhydride and 0.8 mols. of castor oil were heated till the acid value dropped from 200 to 101. A little pyridine was added and heating continued at 110 DEG C. to 200 DEG C. with a further addition of pyridine. A viscous resin with acid value 36.4 was formed. Heated on a steam bath with benzoyl peroxide it set to a solid, flexible state. A solution of the viscous resin in butyl methacrylate also set to an infusible flexible gel when heated at 80 DEG C. with castor oil containing benzoyl peroxide. Examples (2) and (3) are similar, employing different proportions, Example (4) describes the copolymerization of butyl methacrylate with the de-carboxylated castor oil-maleic anhydride esterification product and benzoyl peroxide. Example (5) describes the copolymerization of styrene with a similar esterification product and tertiary butyl peroxide. Heating for 15 hours at 60 DEG C. yielded a flexible gel which became rigid on further heating at higher temperature. The Specification as open to inspection under Sect. 91 covers generally the use of any hydroxylated fatty oil, and refers generally to unsaturated polycarboxylic acids. Aconitic acid is mentioned as suitable. This subject-matter does not appear in the Specification as accepted.
GB579/44A 1943-01-20 1944-01-12 Improvements in and relating to the manufacture of synthetic resins Expired GB592400A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US592400XA 1943-01-20 1943-01-20

Publications (1)

Publication Number Publication Date
GB592400A true GB592400A (en) 1947-09-17

Family

ID=22021696

Family Applications (1)

Application Number Title Priority Date Filing Date
GB579/44A Expired GB592400A (en) 1943-01-20 1944-01-12 Improvements in and relating to the manufacture of synthetic resins

Country Status (1)

Country Link
GB (1) GB592400A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024115988A1 (en) * 2022-12-02 2024-06-06 Apollo Tyres Ltd. Environment-friendly rubber composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024115988A1 (en) * 2022-12-02 2024-06-06 Apollo Tyres Ltd. Environment-friendly rubber composition

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