GB902548A - Improvements in or relating to the manufacture of foamed polyurethanes - Google Patents

Improvements in or relating to the manufacture of foamed polyurethanes

Info

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
Application number
GB1844160A
Inventor
Frank Whitley Lord
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1844160A priority Critical patent/GB902548A/en
Publication of GB902548A publication Critical patent/GB902548A/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

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.
GB1844160A 1960-05-25 1960-05-25 Improvements in or relating to the manufacture of foamed polyurethanes Expired GB902548A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (4)

* Cited by examiner, † Cited by third party
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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