GB929371A - Improvements relating to polyurethane elastomers - Google Patents

Improvements relating to polyurethane elastomers

Info

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
Application number
GB2570/60A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dunlop Rubber Co Ltd
Original Assignee
Dunlop Rubber Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dunlop Rubber Co Ltd filed Critical Dunlop Rubber Co Ltd
Publication of GB929371A publication Critical patent/GB929371A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0008Foam properties flexible
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0041Foam properties having specified density
    • C08G2110/005< 50kg/m3
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00Foam properties
    • C08G2110/0083Foam 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.
GB2570/60A 1959-01-28 1960-01-25 Improvements relating to polyurethane elastomers Expired GB929371A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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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