GB980021A - Production of polymers - Google Patents

Production of polymers

Info

Publication number
GB980021A
GB980021A GB3308260A GB3308260A GB980021A GB 980021 A GB980021 A GB 980021A GB 3308260 A GB3308260 A GB 3308260A GB 3308260 A GB3308260 A GB 3308260A GB 980021 A GB980021 A GB 980021A
Authority
GB
United Kingdom
Prior art keywords
prepolymer
polymer
groups
oxide
ethylene oxide
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
GB3308260A
Inventor
John Fishbein
Paul Ivan Wilson
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
Priority to GB3308260A priority Critical patent/GB980021A/en
Priority to FR874330A priority patent/FR1301785A/en
Publication of GB980021A publication Critical patent/GB980021A/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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4833Polyethers containing oxyethylene units
    • C08G18/4837Polyethers containing oxyethylene units and other oxyalkylene units
    • C08G18/4841Polyethers containing oxyethylene units and other oxyalkylene units containing oxyethylene end groups

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 process for the production of a polyurethane prepolymer comprises reacting in the presence of a catalyst an organic polyisocyanate or polyisothiocyanate with a polymer of an alkylene oxide which when first formed has terminal secondary hydroxyl groups but in which these groups have been reacted with ethylene oxide. Little or no heating is necessary in the preparation. The prepolymer may be converted to a foamed material by addition of water and catalysts. Catalysts specified for the prepolymer formation are tertiary amines, preferably triethylene diamine, and esters, alkyl esters and salts of metals of Group IV, V and VI of the Periodic System. For the foaming step trimethylamine, triethylamine, N-methylmorpholine, N-ethylmorpholine, dimethylbenzylamine and organometallic compounds are suitable catalysts. Silicone oils and water-soluble copolymers of polydimethyl-siloxane and alkylene oxides may also be added. The polymer of alkylene oxide may be a linear polymer of propylene or butylene oxide or may alternatively be a copolymer of these oxides with a polyhydric alcohol such as glycerol, hexanetriol or trimethylol propane. These polymers, containing terminal secondary hydroxyl groups to replace such groups by terminal primary hydroxy groups. Preferably the addition of not less than 1 and not more than 4 ethylene oxide units to each hydroxyl group of the initial propylene or butylene oxide polymer or copolymer is effected. In examples (1) a prepolymer is prepared by mixing an ethylene oxide tipped, glycerol-centred propylene glycol of M.W. 3000, triethylene diamine and a mixture of tolylene-2,4 and 2,6-diisocyanates which is reacted in three portions; (2) a foamed product is obtained when the prepolymer is mixed, in a continuous foaming machine, with a silicone oil and an aqueous solution of N-methylmorpholine and triethylamine.
GB3308260A 1960-09-27 1960-09-27 Production of polymers Expired GB980021A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB3308260A GB980021A (en) 1960-09-27 1960-09-27 Production of polymers
FR874330A FR1301785A (en) 1960-09-27 1961-09-27 Process for preparing polyurethane prepolymers and converting these prepolymers into foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3308260A GB980021A (en) 1960-09-27 1960-09-27 Production of polymers

Publications (1)

Publication Number Publication Date
GB980021A true GB980021A (en) 1965-01-13

Family

ID=10348329

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3308260A Expired GB980021A (en) 1960-09-27 1960-09-27 Production of polymers

Country Status (1)

Country Link
GB (1) GB980021A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4026829A (en) * 1974-08-06 1977-05-31 Sanyo Chemical Industries, Ltd. Flexible polyurethane foam

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4026829A (en) * 1974-08-06 1977-05-31 Sanyo Chemical Industries, Ltd. Flexible polyurethane foam

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