GB953357A - A process for the preparation of urethane modified vegetable oils - Google Patents
A process for the preparation of urethane modified vegetable oilsInfo
- Publication number
- GB953357A GB953357A GB3828860A GB3828860A GB953357A GB 953357 A GB953357 A GB 953357A GB 3828860 A GB3828860 A GB 3828860A GB 3828860 A GB3828860 A GB 3828860A GB 953357 A GB953357 A GB 953357A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oil
- polyisocyanate
- pentaerythritol
- mixture
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/36—Hydroxylated esters of higher fatty acids
Abstract
A process for the preparation of a urethane modified vegetable oil having drying properties is characterized by (a) heating an ethylenically unsaturated triglyceride oil having drying properties with an amount of an aliphatic alcohol containing at least three hydroxyl groups until alcoholysis has occurred with ester interchange to form a diol ester oil system, that is, an ester having two free hydroxyl groups in the molecule, the resultant alcoholized oil having a hydroxyl value in the range 120 to 260, then (b) reacting such diol ester system with a polyisocyanate by contact and at a temperature of 130 DEG F. or less, the ratio of polyisocyanate to the hydroxyl of the oil diol ester system being 0.9 to 1.3 on an equivalent basis until there is 20% or less of the polyisocyanate unreacted and then heating the mixture to above 130 DEG F. until there is less than 1% unreacted polyisocyanate in the mixture, whereby a final product is produced possessing an oil length of 40% to 85%. Specified diol esters are: those of tall oil acids with a mixture of glycerol and pentaerythritol; reaction products of linseed oil with pentaerythritol, tripentaerythritol, trimethylolpropane or glycerine; or a reaction product of pentaerythritol with soy oil or safflower oil. Preferably the reaction with the polyisocyanate is effected in a solvent such as xylene or mineral spirits. Other oils referred to are sesame, poppyseed, sunflower, perilla and corn oils.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3828860A GB953357A (en) | 1960-11-08 | 1960-11-08 | A process for the preparation of urethane modified vegetable oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3828860A GB953357A (en) | 1960-11-08 | 1960-11-08 | A process for the preparation of urethane modified vegetable oils |
Publications (1)
Publication Number | Publication Date |
---|---|
GB953357A true GB953357A (en) | 1964-03-25 |
Family
ID=10402476
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3828860A Expired GB953357A (en) | 1960-11-08 | 1960-11-08 | A process for the preparation of urethane modified vegetable oils |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB953357A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3332896A (en) * | 1963-12-23 | 1967-07-25 | Atlas Chem Ind | Oil-modified polyurethanes |
US3485779A (en) * | 1967-10-19 | 1969-12-23 | Us Agriculture | Diisocyanate modified vegetable oil hydroxyl-terminated polyesteramide coatings |
DE2400490A1 (en) * | 1974-01-05 | 1975-07-17 | Akzo Gmbh | METHOD FOR MANUFACTURING CATIONIC POLYURETHANES |
EP0371294A2 (en) * | 1988-11-22 | 1990-06-06 | Bayer Ag | Use of polyurethane masses for the production of glass fiber containing laminates |
-
1960
- 1960-11-08 GB GB3828860A patent/GB953357A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3332896A (en) * | 1963-12-23 | 1967-07-25 | Atlas Chem Ind | Oil-modified polyurethanes |
US3485779A (en) * | 1967-10-19 | 1969-12-23 | Us Agriculture | Diisocyanate modified vegetable oil hydroxyl-terminated polyesteramide coatings |
DE2400490A1 (en) * | 1974-01-05 | 1975-07-17 | Akzo Gmbh | METHOD FOR MANUFACTURING CATIONIC POLYURETHANES |
EP0371294A2 (en) * | 1988-11-22 | 1990-06-06 | Bayer Ag | Use of polyurethane masses for the production of glass fiber containing laminates |
EP0371294A3 (en) * | 1988-11-22 | 1990-06-20 | Bayer Ag | Process for the preparation of polyurethane masses |
US5286831A (en) * | 1988-11-22 | 1994-02-15 | Bayer Aktiengesellschaft | At least substantially pore-free polyurethane molding compounds |
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