GB974033A - Polyurethane materials - Google Patents
Polyurethane materialsInfo
- Publication number
- GB974033A GB974033A GB1435462A GB1435462A GB974033A GB 974033 A GB974033 A GB 974033A GB 1435462 A GB1435462 A GB 1435462A GB 1435462 A GB1435462 A GB 1435462A GB 974033 A GB974033 A GB 974033A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxide
- alkylene oxide
- tris
- epichlorohydrin
- styrene
- 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
- C08G18/5075—Polyethers having heteroatoms other than oxygen having phosphorus
- C08G18/5078—Polyethers having heteroatoms other than oxygen having phosphorus having phosphorus bound to carbon and/or to hydrogen
-
- 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
- C08G18/5075—Polyethers having heteroatoms other than oxygen having phosphorus
- C08G18/5093—Polyethers having heteroatoms other than oxygen having phosphorus having sulfur in addition to phosphorus
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
Phosphorus containing ethers and polyethers are prepared by reacting an alkylene oxide e.g. in amount 3-120 moles with tris-hydroxymethyl phosphine oxide and/or tris-hydroxymethyl phosphine sulphide. The alkylene oxide may be an aliphatic 1, 2-alkylene oxide e.g. ethylene, propylene, butylene oxides, epichlorohydrin, epibromohydrin or cyclohexene oxide, tetrahydrofuran, styrene or a subtituted styrene oxide. The condensation is usually carried out at 50-250 DEG C. with an acid or basic catalyst. In an example a tris-hydroxy methyl phosphine oxide/epichlorohydrin condensate is prepared by heating the reactants in an autoclave in the presence of N-ethyl morpholine as catalyst. Specifications 816,069 and 892,136 are referredALSO:Flame-retardant polyurethanes are produced by reacting an organic polyisocyanate with a condensation product (A) of at least one alkylene oxide and tris-hydroxymethyl phosphine oxide (T.H.P.O.) and/or tris-hydroxymethylphosphine sulphide (T.H.P.S.) The alkylene oxide may be an aliphatic 1, 2-alkylene oxide e.g. ethylene, propylene or butylene oxides, epichlorohydrin, epibromohydrin or cyclohexene oxide, tetrahydrofuran, styrene or a substituted styrene oxide. The condensation is usually carried out at 50 DEG -250 DEG C. with an acid or basic catalyst and with 3-120 moles of alkylene oxide per mole of phosphorus compound. An organic nonphosphorus-containing polyhydronyl compound may also be present e.g. a polyether, polyester or polyesteramide containing 2-4 hydroxyl groups and having a molecular weight of at least 400 preferably 1,000-4,000. The condensation product (A) may be present in amount to provide 0.1 to 20% by weight of phosphorus in the polymethane. Water may be present to give a foamed product. Tertiary amines and/or organo-tin compounds and silicone oils may be added as catalysts and cell controlling agents. In the examples a T.H.P.O./epichlorohydrin condensation product was added to (1) a glycerolpropylene oxide condensate and toluene diisocyanate, a silicone, dibutyltin dilaurate, triethylene diamine, N-ethylmorpholine and water (3) a condensate of propylene oxide with a polyhydric alcohol ("Daltolac 41" Registered Trade Mark) (5) a polyester (Daltolac 21) and an octyl phenol/ethylene oxide surfactant. Specifications 816,069 and 892,136 are referred to.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1435462A GB974033A (en) | 1962-04-13 | 1962-04-13 | Polyurethane materials |
DEA42834A DE1208485B (en) | 1962-04-13 | 1963-04-05 | Process for the production of optionally foamed polyurethanes |
FR931465A FR1368775A (en) | 1962-04-13 | 1963-04-12 | Process for preparing polyurethanes, products thus obtained and their applications |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1435462A GB974033A (en) | 1962-04-13 | 1962-04-13 | Polyurethane materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB974033A true GB974033A (en) | 1964-11-04 |
Family
ID=10039686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1435462A Expired GB974033A (en) | 1962-04-13 | 1962-04-13 | Polyurethane materials |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1208485B (en) |
GB (1) | GB974033A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3445405A (en) * | 1965-06-01 | 1969-05-20 | Wyandotte Chemicals Corp | Flame-resistant polyurethane compositions |
CN115232287A (en) * | 2022-08-08 | 2022-10-25 | 南京金栖化工集团有限公司 | Flame-retardant slow-rebound polyurethane sponge and preparation method thereof |
WO2022238293A1 (en) * | 2021-05-11 | 2022-11-17 | Clariant International Ltd | Flexible foams comprising flame-retardant polyurethane, a process for their production and use thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10304344B4 (en) * | 2003-02-03 | 2015-09-10 | Basf Se | Flame retardant polyurethanes |
-
1962
- 1962-04-13 GB GB1435462A patent/GB974033A/en not_active Expired
-
1963
- 1963-04-05 DE DEA42834A patent/DE1208485B/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3445405A (en) * | 1965-06-01 | 1969-05-20 | Wyandotte Chemicals Corp | Flame-resistant polyurethane compositions |
WO2022238293A1 (en) * | 2021-05-11 | 2022-11-17 | Clariant International Ltd | Flexible foams comprising flame-retardant polyurethane, a process for their production and use thereof |
CN117222684A (en) * | 2021-05-11 | 2023-12-12 | 科莱恩国际有限公司 | Flexible foam comprising flame-retardant polyurethane, method for the production thereof and use thereof |
CN115232287A (en) * | 2022-08-08 | 2022-10-25 | 南京金栖化工集团有限公司 | Flame-retardant slow-rebound polyurethane sponge and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
DE1208485B (en) | 1966-01-05 |
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