GB929371A - Improvements relating to polyurethane elastomers - Google Patents
Improvements relating to polyurethane elastomersInfo
- Publication number
- GB929371A GB929371A GB2570/60A GB257060A GB929371A GB 929371 A GB929371 A GB 929371A GB 2570/60 A GB2570/60 A GB 2570/60A GB 257060 A GB257060 A GB 257060A GB 929371 A GB929371 A GB 929371A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepolymer
- mixture
- reaction
- polypropylene glycol
- viscosity
- 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
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0008—Foam properties flexible
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0041—Foam properties having specified density
- C08G2110/005—< 50kg/m3
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
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
A method of preparing a prepolymer comprises reacting a polyether, polyester or polyesteramide having primary, secondary or tertiary hydroxyl groups in molecular chain terminal positions by agitating therewith, without the application of heat, an aromatic polyisocyanate in an amount which is sufficient, or substantially sufficient, to make an isocyanate group available for reaction with each of the hydroxyl groups, allowing the reaction to follow its course until the heat evolved is dissipated, heating the reaction mixture progressively to a temperature of the order of from 70 DEG to 120 DEG C. and adding gradually a second amount of aromatic polyisocyanate so that the final prepolymer contains free isocyanate groups and cooling the resulting prepolymer. The second addition is preferably controlled so that the viscosity of the mixture stays constant. A foamed polyurethane elastomer is obtained by mixing the prepolymer at room temperature with water and one or more catalysts and preferably with a foam stabilizing agent. N-ethyl- and methyl-morpholines, triethylamine and trimethylamine are suitable catalysts. In Example (1) polypropylene glycol is reacted with toluene 2:4- and 2:6-diisocyanates in amount calculated to react the OH groups without application of heat, the temperature rising to 40 DEG C. When the exothermic reaction has finished the mixture is heated progressively to 100 DEG C. until the viscosity is 12,000 centipoises and more of the toluene diisocyanate is then added in such a way that the viscosity remains constant. The prepolymer is rapidly cooled to 35 DEG to 40 DEG C. and a small addition of diisocyanate is made. Foaming is carried out by adding an aqueous solution of N-methylmorpholine and triethylamine. In Example (2) a similar process using a mixture of polypropylene glycol and a polypropylene glycol triol as starting material is described.ALSO:A method of preparing a prepolymer comprises reacting a polyether, polyester or polyesteramide having primary, secondary or tertiary hydroxyl groups in molecular chain terminal positions by agitating therewith, without the application of heat, an aromatic polyisocyanate in an amount which is sufficient or substantially sufficient to make an isocyanate group available for reaction with each of the hydroxyl groups, allowing the reaction to follow its course until the heat evolved is dissipated, heating the reaction mixture progressively to a temperature of the order of from 70 DEG C. to 120 DEG C. and adding gradually a second amount of aromatic polyisocyanate so that the final prepolymer contains free isocyanate groups and cooling the resulting prepolymer. The second addition is preferably controlled so that the viscosity of the mixture stays constant. A foamed polyurethane elastomer is obtained by mixing the prepolymer at room temperature with water and one or more catalysts and preferably with a foam stabilizing agent. N-Ethyl- and methyl-morpholines triethylamine and trimethylamine are suitable catalysts. In Example (1) polypropylene glycol is reacted with toluene 2 : 4- and 2 : 6-diisocyanates in amount calculated to react the OH groups without application of heat, the temperature rising to 40%C. When the exothermic reaction has finished the mixture is heated progressively to 100 DEG C. until the viscosity is 12000 centipoises and more of the toluene diisocyanate is then added in such a way that the viscosity remains constant. The prepolymer is rapidly cooled to 35 DEG C. to 40 DEG C. and a small addition of diisocyanate is made. Foaming is carried out by adding an aqueous solution of N-methyl-morpholine and triethylamine. In Example (2) a similar process using a mixture of polypropylene glycol and a polypropylene glycol triol as starting material is described.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR785187A FR1227279A (en) | 1959-01-28 | 1959-01-28 | Improvement in the manufacture of flexible or elastic synthetic materials, in particular cellular materials of this type |
Publications (1)
Publication Number | Publication Date |
---|---|
GB929371A true GB929371A (en) | 1963-06-19 |
Family
ID=8710594
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2570/60A Expired GB929371A (en) | 1959-01-28 | 1960-01-25 | Improvements relating to polyurethane elastomers |
Country Status (3)
Country | Link |
---|---|
FR (1) | FR1227279A (en) |
GB (1) | GB929371A (en) |
MY (1) | MY6400044A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4125545A (en) * | 1976-07-19 | 1978-11-14 | N L Industries, Inc. | Stabilized diphenylmethane diisocyanate prepolymer |
CN113801598A (en) * | 2020-02-07 | 2021-12-17 | 昆山优瑞森医疗科技有限公司 | Pressure-reducing pad for preventing pressure sores and preparation method thereof |
-
1959
- 1959-01-28 FR FR785187A patent/FR1227279A/en not_active Expired
-
1960
- 1960-01-25 GB GB2570/60A patent/GB929371A/en not_active Expired
-
1964
- 1964-12-31 MY MY196444A patent/MY6400044A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4125545A (en) * | 1976-07-19 | 1978-11-14 | N L Industries, Inc. | Stabilized diphenylmethane diisocyanate prepolymer |
CN113801598A (en) * | 2020-02-07 | 2021-12-17 | 昆山优瑞森医疗科技有限公司 | Pressure-reducing pad for preventing pressure sores and preparation method thereof |
CN113801598B (en) * | 2020-02-07 | 2023-06-06 | 昆山优瑞森医疗科技有限公司 | Pressure-reducing pad for preventing pressure sores and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
MY6400044A (en) | 1964-12-31 |
FR1227279A (en) | 1960-08-19 |
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