GB1139575A - Stabilised mixtures containing trialkanolamines and halogenated hydrocarbons - Google Patents
Stabilised mixtures containing trialkanolamines and halogenated hydrocarbonsInfo
- Publication number
- GB1139575A GB1139575A GB2727565A GB2727565A GB1139575A GB 1139575 A GB1139575 A GB 1139575A GB 2727565 A GB2727565 A GB 2727565A GB 2727565 A GB2727565 A GB 2727565A GB 1139575 A GB1139575 A GB 1139575A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyol
- halogenated hydrocarbon
- trialkanolamine
- thiobis
- polyisocyanate
- 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
-
- 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
- C08G18/6603—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6614—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38
- C08G18/6622—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 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)
- Polyurethanes Or Polyureas (AREA)
Abstract
1,139,575. Polyurethane foams. IMPERIAL CHEMICAL INDUSTRIES Ltd. 14 June, 1966 [28 June, 1965], No. 27275/65. Headings C3C and C3R. Polyurethane foams are prepared by reacting an organic polyisocyanate with a polyol having a molecular weight of at least 300 in the presence of a trialkanolamine, a halogenated hydrocarbon and 0.1 to 5% by weight of the trialkanolamine and halogenated hydrocarbon of a thiobisphenol. The trialkanolamine halogenated hydrocarbon and thiobisphenol are suitably mixed together and then added to the polyisocyanate and polyol or, if desired, they may be mixed with the polyol and the resulting mixture reacted with the polyisocyanate. Suitable polyisocyanates are the tolylene diisooyanatea and 4,41-diphenylmethane diisocyanate. The exemplified polyol is an oxypropylated trimethylolpropane. Examples of trialkanolamines are triethanolamine, triisopropanolamine or the reaction products of propylene oxide with mono- and diethanolamine. The halogenated hydrocarbon preferably has a b.p. not exceeding 75‹ C., e.g. methylene chloride, vinylidene chloride and particularly compounds containing at least one fluorine atom per molecule. Preferred thiobisphenols are 2,21-thiobis-(6-methylphenol), 2,2<SP>1</SP>- thiobis - (4 - methyl - 6 - tert.- butylphenol) and 4,4<SP>1</SP>-thiobis-(3-methyl-6-tert.- butylphenol). The foam forming reaction mixture may also contain e.g. water, catalysts, surface-active agents and flame retardants.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2727565A GB1139575A (en) | 1965-06-28 | 1965-06-28 | Stabilised mixtures containing trialkanolamines and halogenated hydrocarbons |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2727565A GB1139575A (en) | 1965-06-28 | 1965-06-28 | Stabilised mixtures containing trialkanolamines and halogenated hydrocarbons |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1139575A true GB1139575A (en) | 1969-01-08 |
Family
ID=10256928
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2727565A Expired GB1139575A (en) | 1965-06-28 | 1965-06-28 | Stabilised mixtures containing trialkanolamines and halogenated hydrocarbons |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1139575A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2231704A1 (en) * | 1973-05-30 | 1974-12-27 | Montedison Spa |
-
1965
- 1965-06-28 GB GB2727565A patent/GB1139575A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2231704A1 (en) * | 1973-05-30 | 1974-12-27 | Montedison Spa |
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