GB914414A - A method for the preparation of a urethane modified ethylenically unsaturated vegetable oil - Google Patents

A method for the preparation of a urethane modified ethylenically unsaturated vegetable oil

Info

Publication number
GB914414A
GB914414A GB3828760A GB3828760A GB914414A GB 914414 A GB914414 A GB 914414A GB 3828760 A GB3828760 A GB 3828760A GB 3828760 A GB3828760 A GB 3828760A GB 914414 A GB914414 A GB 914414A
Authority
GB
United Kingdom
Prior art keywords
diol
oil
pentaerythritol
ester
diol ester
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
GB3828760A
Inventor
Donald James Waythomas
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.)
Textron Inc
Original Assignee
Textron Inc
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
Priority to US770259A priority Critical patent/US3022327A/en
Application filed by Textron Inc filed Critical Textron Inc
Priority to GB3828760A priority patent/GB914414A/en
Publication of GB914414A publication Critical patent/GB914414A/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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/36Hydroxylated esters of higher fatty acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A method for the preparation of a urethane modified ethylenically unsaturated vegetable oil having drying properties is characterized by reacting a diisocyanate and a diol system comprising a diol ester of an ethylenically unsaturated vegetable oil and 3 to 18% based upon the weight of the diol ester of a diol in which the hydrocarbon groups are separated by not more than 4 carbon atoms and having a molecular weight of less than 120, the amount of diisocyanate employed being substantially equivalent to the total hydroxyl of the diol system and the amount of diol ester being sufficient to produce a final oil length of 30 to 80%, the reaction being continued under heating until the resultant urethane modified oil possesses substantially no free isocyanate. The reaction is usually performed in an inert organic solvent, and may be effected in two stages, the addition of reactants and first heating taking place below 130 DEG F. and the final stage at above 130 DEG F. Linseed, safflower, perilla, tall and soybean oils are specified vegetable oils. Glycerine, pentaerythritol and trimethylol propane or ethane are suitable polyols for the preparation of the diol ester. In examples (1) a modified drying oil is produced as a semi-solid by reacting a diol ester (from linseed oil and pentaerythritol), propylene glycol (or a butane diol) and tolylene diisocyanate; (2) a similar reaction is effected in aromatic or mineral spirits solvent solution; (3) similarly reacted are a diol ester (from pentaerythritol, glycerine and distilled tall oil fatty acids), 2,4-pentanediol and tolylene diisocyanate in xylene solution; (4) a dihydroxy ester (from soybean oil and pentaerythritol), 1,3-butylene glycol and tolylene diisocyanate are reacted.
GB3828760A 1958-10-29 1960-11-08 A method for the preparation of a urethane modified ethylenically unsaturated vegetable oil Expired GB914414A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US770259A US3022327A (en) 1958-10-29 1958-10-29 Urethane modified vegetable oil
GB3828760A GB914414A (en) 1960-11-08 1960-11-08 A method for the preparation of a urethane modified ethylenically unsaturated vegetable oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3828760A GB914414A (en) 1960-11-08 1960-11-08 A method for the preparation of a urethane modified ethylenically unsaturated vegetable oil

Publications (1)

Publication Number Publication Date
GB914414A true GB914414A (en) 1963-01-02

Family

ID=10402465

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3828760A Expired GB914414A (en) 1958-10-29 1960-11-08 A method for the preparation of a urethane modified ethylenically unsaturated vegetable oil

Country Status (1)

Country Link
GB (1) GB914414A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4267081A (en) * 1978-10-23 1981-05-12 Ameron, Inc. High solids polyurethane coatings

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4267081A (en) * 1978-10-23 1981-05-12 Ameron, Inc. High solids polyurethane coatings

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