GB840500A - Process for the production of urethane polyisocyanates - Google Patents
Process for the production of urethane polyisocyanatesInfo
- Publication number
- GB840500A GB840500A GB13082/58A GB1308258A GB840500A GB 840500 A GB840500 A GB 840500A GB 13082/58 A GB13082/58 A GB 13082/58A GB 1308258 A GB1308258 A GB 1308258A GB 840500 A GB840500 A GB 840500A
- Authority
- GB
- United Kingdom
- Prior art keywords
- isocyanate
- column
- mixture
- extracted
- polyhydric alcohol
- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/80—Masked polyisocyanates
- C08G18/8003—Masked polyisocyanates masked with compounds having at least two groups containing active hydrogen
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
In a process of producing urethane polyisocyanates having a high content of available -NCO, but which do not emit toxic vapours, by reacting an organic di-isocyanate with a polyhydric alcohol, the proportions of the two reactants being such that there is more than 1 mol. of di-isocyanate for each hydroxyl group of the polyhydric alcohol whereby the formation of polymeric products of high molecular weight is minimized, the liquid reaction mixture is extracted, preferably at a temperature between 50 DEG C. and 130 DEG C., with a liquid aliphatic and/or alicyclic hydrocarbon, or a mixture of such hydrocarbons, in order to dissolve out unreacted di-isocyanate from the urethane polyisocyanate product. Hexanes, cyclohexane, the alkyl cyclohexanes, heptanes, octanes, gasoline fractions and synthetic hydrocarbon fractions are the preferred extraction media. In an example, a mixture of toluylene-2,4-di-isocyanate and toluylene-2,6-di-isocyanate is heated to 90 DEG C.; and a mixture comprising trimethylol propane and 1,3-butylene glycol is added over a period of 2 1/2 hrs. while maintaining the temperature at about 88 DEG to 100 DEG C. The resulting urethane polyisocyanate, dissolved in excess toluylene diisocyanate, is then extracted with a solvent (boiling range 315-390 DEG F.) comprising about 88% paraffins and naphthenes and about 11.5% aromatics. The extraction is carried out in an externally heated vertical column divided into seven sections, each containing a turbineagitator. The polyisocyanate is fed continuously into the top of the column, while the solvent is introduced into the bottom; the temperature of the column being held in the range of 100 DEG to 116 DEG C. The extracted product, withdrawn from the bottom of the column, is heated in vacuo to remove solvent. The final product is an amber solid which contains 18.5% available NCO. Other polyhydric alcohols which may be reacted with organic diisocyanates are: pentaerythritol, triethanolamine, neopentyl glycol, and castor oil. It is also possible to use, together with the polyhydric alcohol, a small amount of a higher-molecular polyhydroxy compound, such as hydroxyl polyesters or hydroxyl polyethers.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US840500XA | 1957-04-29 | 1957-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB840500A true GB840500A (en) | 1960-07-06 |
Family
ID=22182570
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB13082/58A Expired GB840500A (en) | 1957-04-29 | 1958-04-24 | Process for the production of urethane polyisocyanates |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB840500A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114195974A (en) * | 2021-12-06 | 2022-03-18 | 季华实验室 | Polyurethane prepolymer and preparation method thereof, and polyurethane product |
-
1958
- 1958-04-24 GB GB13082/58A patent/GB840500A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114195974A (en) * | 2021-12-06 | 2022-03-18 | 季华实验室 | Polyurethane prepolymer and preparation method thereof, and polyurethane product |
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