GB981135A - Improvements in the manufacture of cellular polyurethanes - Google Patents
Improvements in the manufacture of cellular polyurethanesInfo
- Publication number
- GB981135A GB981135A GB4125862A GB4125862A GB981135A GB 981135 A GB981135 A GB 981135A GB 4125862 A GB4125862 A GB 4125862A GB 4125862 A GB4125862 A GB 4125862A GB 981135 A GB981135 A GB 981135A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diisocyanate
- methyl
- reaction mixture
- oxide
- per molecule
- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6681—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
- C08G18/6688—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3271
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Fireproofing Substances (AREA)
Abstract
Foamed polyurethanes may be prepared by reacting an organic polyisocyanate and a polyether containing at least two ether groups and two hydroxy groups per molecule, under such conditions that a foam forming gas is generated, and having in the reaction mixture an N-substituted dialkanolamine in an amount of at least 15% by weight of the polyether. The preferred polyethers are polymers and copolymers of ethylene oxide or propylene oxide, optionally prepared by polymerization in the presence of a substance having two or more active hydrogen atoms per molecule, such as ammonia and polydroxy compounds such as glycerol, triethanolamine and polyamines such as ethylene diamine and tolylene diamine. Other alkylene oxides may be used such as 1:2 butylene oxide and 2:3 butylene oxide. Many aliphatic and aromatic diisocyanates are listed as suitable polyisocyanates such as hexamethylene diisocyanate and tolylene 2:4-diisocyanate. Triisocyanate may also be used such as 2:4:6-triisocyanateotoluene. The foam forming gas may be generated by adding water to the reaction mixture to react with a proportion of the diisocyanate to produce carbon dioxide, or by incorporating a low boiling liquid having a boiling point not exceeding 75 DEG C. which will volatilize on heating. A combination of these two methods may be employed. Preferred low boiling liquids are halogenated alkanes containing fluorine, such as monofluorotrichloromethane, dibromodifluoromethane, 1:1:1 - trichloro - 2:2:2 - trifluoroethane, dichlorodifluoromethane, dichloromonofluoromethane, dichlorotetrafluoroethane, monochlorodifluoromethane, trifluoroethylbromide and mixtures thereof. Examples of suitable N-substituted dialkanolamines include N - methyl diethanolamine, N - ethyldiethanolamine, N-butyl diethanolamine, N-phenyldiethanolamine and N-methyl diisopropanolamine. Other additives which may be included are catalysts such as tertiary amines and soluble organic compounds of heavy metals such as iron and manganese acetyl acetonate, lead actoate, dibutyl tin dilaurate and stannous octoate, surface active agents, e.g. oxethylated phenols, oleyl alcohol, sulphated methyl oleate, polyalkyl or polaryl siloxanes and siloxane-oxyalkylene copolymers, flame retardants such as b -trichloroethylphosphate and dioctylphthalate, colouring matters and fillers such as carbon black and silica and colour stabilizers, whitening agents, and anti-oxidants such as tert-butylalcohol and sterically hindered phenols.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4125862A GB981135A (en) | 1962-10-31 | 1962-10-31 | Improvements in the manufacture of cellular polyurethanes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4125862A GB981135A (en) | 1962-10-31 | 1962-10-31 | Improvements in the manufacture of cellular polyurethanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB981135A true GB981135A (en) | 1965-01-20 |
Family
ID=10418867
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4125862A Expired GB981135A (en) | 1962-10-31 | 1962-10-31 | Improvements in the manufacture of cellular polyurethanes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB981135A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4256802A (en) * | 1979-06-11 | 1981-03-17 | The Upjohn Company | Process for polyisocyanurate foams suitable for panels |
EP0079115A1 (en) * | 1981-10-28 | 1983-05-18 | Imperial Chemical Industries Plc | Polymer-modified polyols |
WO1986001522A1 (en) * | 1984-08-23 | 1986-03-13 | The Dow Chemical Company | An active hydrogen-containing composition containing a dialkanol tertiary amine and a process for preparing a polyurethane foam |
JPS61501327A (en) * | 1984-08-23 | 1986-07-03 | ザ ダウ ケミカル カンパニ− | Active hydrogen-containing composition containing dialkanol tertiary amine |
-
1962
- 1962-10-31 GB GB4125862A patent/GB981135A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4256802A (en) * | 1979-06-11 | 1981-03-17 | The Upjohn Company | Process for polyisocyanurate foams suitable for panels |
EP0079115A1 (en) * | 1981-10-28 | 1983-05-18 | Imperial Chemical Industries Plc | Polymer-modified polyols |
WO1986001522A1 (en) * | 1984-08-23 | 1986-03-13 | The Dow Chemical Company | An active hydrogen-containing composition containing a dialkanol tertiary amine and a process for preparing a polyurethane foam |
JPS61501327A (en) * | 1984-08-23 | 1986-07-03 | ザ ダウ ケミカル カンパニ− | Active hydrogen-containing composition containing dialkanol tertiary amine |
US4632943A (en) * | 1984-08-23 | 1986-12-30 | Dow Chemical Company | Polyurethane foams prepared from alkyl dialkanol amine-containing polyols |
JPH0154364B2 (en) * | 1984-08-23 | 1989-11-17 | Dow Chemical Co |
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