GB1049288A - Polyurethanes - Google Patents
PolyurethanesInfo
- Publication number
- GB1049288A GB1049288A GB2720262A GB2720262A GB1049288A GB 1049288 A GB1049288 A GB 1049288A GB 2720262 A GB2720262 A GB 2720262A GB 2720262 A GB2720262 A GB 2720262A GB 1049288 A GB1049288 A GB 1049288A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyether
- hydroxyl ended
- hydroxyl
- hydroxyethylamino
- triazine
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
- C08G18/5054—Polyethers having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring
- C08G18/5063—Polyethers having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring containing three nitrogen atoms in the ring
Abstract
A polyether of OH No. 343 is prepared by reacting tris (di-b -hydroxyethylamino) 1:3:5 triazine with propylene oxide, the latter being added in two stages.ALSO:Polyurethanes are prepared by reacting an organic polyisocyanate and a hydroxyl ended polyether of formula <FORM:1049288/C3/1> wherein R, R1, R11, R111, RIV and RV each stand for a hydrogen atom, an alkyl group or a hydroxyl ended polyether chain, at least two of the groups R being hydroxyl ended polyether chains. The hydroxyl ended polyether may have a M.W. of 300-10,000 and may be the oxyalkylation product of a hydroxy alkyl derivative of melamine. In the preparation of foams, surface coatings and adhesives the hydroxy ended polyether preferably contains at least three isocyanate reactive groupings. In an example a polyether of OH No. 343 was prepared from tris(di-b -hydroxyethylamino)-1:3:5-triazine and propylene oxide, the latter being added in two stages. The polyether was mixed with water, butylated urea formaldehyde, cyclohexanone, methyl isobutyl ketone and a solution of a phosgenated crude diaminodiphenylmethane to obtain a coating solution.ALSO:Substrates e.g. wood, rubber, metals, glass and fabrics are coated with a polyurethane coating composition obtained by reacting an organic polyisocyanate with a polyether of formula <FORM:1049288/B1-B2/1> where the groups R each stand for hydrogen, alkyl or a hydroxyl ended polyether chain, at least two of the groups R being hydroxyl ended polyether chains. In an example a polyurethane obtained from propoxylated tris (di-b hydroxyethylamino) - 1 : 3 : 5 triazine by reaction with a phosgenated crude diamino diphenylmethane in admixture with water, xylene, cyclhexanone, methyl isobutyl ketone, and butylated urea formaldehyde was applied by spinning to steel panels or by dipping to steel rods and dried.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2720262A GB1049288A (en) | 1962-07-16 | 1962-07-16 | Polyurethanes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2720262A GB1049288A (en) | 1962-07-16 | 1962-07-16 | Polyurethanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1049288A true GB1049288A (en) | 1966-11-23 |
Family
ID=10255840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2720262A Expired GB1049288A (en) | 1962-07-16 | 1962-07-16 | Polyurethanes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1049288A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1279686A2 (en) * | 2001-07-26 | 2003-01-29 | Agrolinz Melamin GmbH | Polymers from triazine derivatives |
EP2128144A1 (en) * | 2008-05-30 | 2009-12-02 | Basf Se | Amphiphilic molecules with a triazine core |
WO2009144274A2 (en) * | 2008-05-30 | 2009-12-03 | Basf Se | Amphiphilic molecules with a triazine core |
CN107602789A (en) * | 2017-09-29 | 2018-01-19 | 鹤山市杰之星五金实业有限公司 | A kind of plant polyatomic alcohol and its soft polyurethane foam containing plant polyatomic alcohol |
CN112552979A (en) * | 2020-11-27 | 2021-03-26 | 广东石油化工学院 | Antiwear agent and preparation method thereof |
-
1962
- 1962-07-16 GB GB2720262A patent/GB1049288A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1279686A2 (en) * | 2001-07-26 | 2003-01-29 | Agrolinz Melamin GmbH | Polymers from triazine derivatives |
EP1279686A3 (en) * | 2001-07-26 | 2004-01-14 | Agrolinz Melamin GmbH | Polymers from triazine derivatives |
EP2128144A1 (en) * | 2008-05-30 | 2009-12-02 | Basf Se | Amphiphilic molecules with a triazine core |
WO2009144274A2 (en) * | 2008-05-30 | 2009-12-03 | Basf Se | Amphiphilic molecules with a triazine core |
WO2009144274A3 (en) * | 2008-05-30 | 2010-05-14 | Basf Se | Amphiphilic molecules with a triazine core |
CN107602789A (en) * | 2017-09-29 | 2018-01-19 | 鹤山市杰之星五金实业有限公司 | A kind of plant polyatomic alcohol and its soft polyurethane foam containing plant polyatomic alcohol |
CN112552979A (en) * | 2020-11-27 | 2021-03-26 | 广东石油化工学院 | Antiwear agent and preparation method thereof |
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