GB902548A - Improvements in or relating to the manufacture of foamed polyurethanes - Google Patents
Improvements in or relating to the manufacture of foamed polyurethanesInfo
- Publication number
- GB902548A GB902548A GB1844160A GB1844160A GB902548A GB 902548 A GB902548 A GB 902548A GB 1844160 A GB1844160 A GB 1844160A GB 1844160 A GB1844160 A GB 1844160A GB 902548 A GB902548 A GB 902548A
- Authority
- GB
- United Kingdom
- Prior art keywords
- isocyanate reactive
- polyethers
- polyisocyanates
- reactive groups
- organic
- 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
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
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
Foamed polyurethanes are obtained by reacting hydroxyl group-containing polyethers containing at least two isocyanate reactive groups per molecule with organic polyisocyanates in the presence of (1) a gas-forming agent such as water or a non-isocyanate reactive organic liquid with a boiling point not exceeding 75 DEG C. and (2) a pre-formed reaction product of a polyester, polyesteramide or polyether containing at least two isocyanate reactive groups per molecule with an organic polyisocyanate in an amount such that at least one isocyanate group is used for every two isocyanate reactive groups in the polyester polyesteramide or polyether. Numerous polyisocyanates and reactants for preparing the polyesters, polyesteramides and polyethers are specified; the polyisocyanates and polyethers may be used to prepare the pre-polymer as well as taking part in the main reaction. Organic gas-forming agents specified include acetone, methylene dichloride and chlorofluoro- and bromofluoro-alkanes. Addition constituents of the main reaction mixture include catalysts dimethylbenzylamine, dimethylcyclohexylamine, triethylene diamine, and salts of these amines with lactic or oxalic acid, manganese and iron acetylacetonates, dibutyl tin dilaurate and stannous octoate surface-active agents oxyethylated phenols such as octyl phenol, oxyethylated fatty alcohols such as cetyl alcohol, fatty acid salts such as diethylamine oleate, sulphated hydrocarbon chain-containing substances such as sulphated methyl oleate and silicone oils such as polydimethylsiloxane and polyoxyalkylene-polysiloxane block copolymers flame proofing agents trichloroethyl phosphate and antimony oxide. In the examples, the polyurethane foam is prepared from reaction mixtures containing (1) oxypropylated sucrose, water, a condensate of an alkyl cresol with ethylene oxide, dibutyl tin dilaurate, dimethylcyclohexylamine, 4:41-diisocyanato-diphenylmethane and (2) oxypropylated glycerol, water, a condensate of an alkyl cresol with ethylene oxide, b -trichloroethyl phosphate, 4:41-diisocyanato-diphenylmethane, and a prepolymer prepared from a polypropylene glycol and a mixture of 2:4- and 2:6-tolylene diisocyanates.ALSO:Foamed polyurethanes are obtained by reacting hydroxyl groupcontaining polyethers containing at least two isocyanate reactive groups per molecule with organic polyisocyanates in the presence of (1) a gas-forming agent such as water or a non-isocyanate reactive organic liquid with a boiling point not exceeding 75 DEG C. and (2) a pre-formed reaction product of a polyester, polyesteramide or polyether containing at least two isocyanate reactive groups per molecule with an organic polyisocyanate in an amount such that at least one isocyanate group is used for every two isocyanate reactive groups in the polyester, polyesteramide or polyether. Numerous polyisocyanates and reactants for preparing the polyesters, polyesteramides and polyethers are specified; the polyisocyanates and polyethers may be used to prepare the pre-polymer as well as taking part in the main reaction. Organic gas-forming agents specified include acetone, methylene dichloride and chlorofluoro- and bromofluoro-alkanes. Addition constituents of the main reaction mixture include catalysts dimethylbenzylamine, dimethylcyclohexylamine, triethylene diamine and salts of these amines with lactic or oxalic acid, manganese and iron acetylacetonates, dibutyl tindilaurate and stannous octoate surface active agents: oxyethylated phenols such as octyl phenol, oxyethylated fatty alcohols such as cetyl alcohol, fatty acid salts such as diethylamine oleate, sulphated hydro-carbon chain-containing substances such as sulphated methyl oleate and silicone oils such as polydimethylsiloxane and polyoxyalkylene-polysiloxane block copolymers flame proofing agents: trichloroethyl phosphate and antimony oxide. In the examples, the polyurethane foam is prepared from reaction mixtures containing (1) oxypropylated sucrose, water, a condensate of an alkyl cresol with ethylene oxide, di-butyl tindilaurate, dimethylcyclohexylamine, 4 : 41-diisocyanatodiphenylmethane and a prepolymer prepared from oxypropylated glycerol and 4 : 41-diisocyanato-diphenylmethane and (2) oxypropylated glycerol, water, a condensate of an alkylcresol with ethylene oxide, b -trichloroethyl phosphate, 4 : 41-diisocyanate-diphenylmethane, and a prepolymer prepared from a polypropylene glycol and a mixture of 2 : 4-and 2 : 6- tolylene diisocyanates.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1844160A GB902548A (en) | 1960-05-25 | 1960-05-25 | Improvements in or relating to the manufacture of foamed polyurethanes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1844160A GB902548A (en) | 1960-05-25 | 1960-05-25 | Improvements in or relating to the manufacture of foamed polyurethanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB902548A true GB902548A (en) | 1962-08-01 |
Family
ID=10112490
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1844160A Expired GB902548A (en) | 1960-05-25 | 1960-05-25 | Improvements in or relating to the manufacture of foamed polyurethanes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB902548A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2214720A1 (en) * | 1973-01-19 | 1974-08-19 | Ici Ltd | |
EP0547515A2 (en) † | 1991-12-17 | 1993-06-23 | Takeda Chemical Industries, Ltd. | Method for producing open cell rigid polyurethane foam |
US6433032B1 (en) | 1998-04-02 | 2002-08-13 | Imperial Chemical Industries Plc | Process for rigid polyurethane foams |
-
1960
- 1960-05-25 GB GB1844160A patent/GB902548A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2214720A1 (en) * | 1973-01-19 | 1974-08-19 | Ici Ltd | |
EP0547515A2 (en) † | 1991-12-17 | 1993-06-23 | Takeda Chemical Industries, Ltd. | Method for producing open cell rigid polyurethane foam |
EP0547515B2 (en) † | 1991-12-17 | 2001-08-16 | Takeda Chemical Industries, Ltd. | Method for producing open cell rigid polyurethane foam |
US6433032B1 (en) | 1998-04-02 | 2002-08-13 | Imperial Chemical Industries Plc | Process for rigid polyurethane foams |
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