GB890280A - 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
GB890280A
GB890280A GB650659A GB650659A GB890280A GB 890280 A GB890280 A GB 890280A GB 650659 A GB650659 A GB 650659A GB 650659 A GB650659 A GB 650659A GB 890280 A GB890280 A GB 890280A
Authority
GB
United Kingdom
Prior art keywords
pentanediono
diisocyanate
tetrakis
zirconium
specified
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
GB650659A
Inventor
Kenneth Stephenson
Harry James Twitchett
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 GB650659A priority Critical patent/GB890280A/en
Publication of GB890280A publication Critical patent/GB890280A/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
    • C08G18/16Catalysts
    • C08G18/22Catalysts containing metal compounds
    • C08G18/222Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26

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 made by reacting together an organic polyisocyanate and a hydroxyl-ended polymer in the presence of a co-ordination compound of titanium, zirconium, hafnium, thorium or manganese with a b -diketone, b -ketoester or b -hydroxyaldehyde, to give a reaction product containing free isocyanate groups which is then reacted with water. Specified co-ordinating compounds are acetylacetone, benzoylacetone, 3-cyanoacetylacetone, dibenzoylacetone, propionylacetone, trifluoroacetylacetone, methyl acetoacetate, ethyl acetoacetate, propyl acetoacetate and salicylaldehyde. Specified polyisocyanates include hexamethylene diisocyanate, tolylene diisocyanates, diphenyl methane-4:41-diisocyanate, 3-methyl diphenyl methane-4:41-diisocyanate, m- and p-phenylene diisocyanates, chlorophenylene-2:4-diisocyanate, dicyclohexyl methane diisocyanate, 2:4:6-triisocyanato toluene and 2:4:4-triisocyanatodiphenyl ether. Specified hydroxyl-ended polymers are polyesters, polyesteramides and polyethers of which many are listed. The reaction may be continuous or discontinuous and may be effected in the presence of catalysts, non-ionic surfaceactive agents, salts of sulphuric acid derivatives of high molecular weight organic compounds, silicone oils, foam stabilizing agents, e.g. ethyl cellulose, certain polyhydroxy compounds, e.g. trimethylol propane, pigments, plasticizers, e.g. dinonyl phthalate and fire-proofing agents, e.g. tri-(b -chloroethyl) phosphate. The stability of the intermediate reaction products may be improved by the addition thereto of acid-reacting substances, e.g. acetyl chloride. In the Examples, mixed tolylene 2:4- and 2:6-diisocyanates are reacted with polypropylene glycol in the presence of:- (1) tris-(2:4-pentanediono) manganese III; (2) tetrakis-(2:4-pentanediono) zirconium IV; (3) a polyether derived from propylene oxide and 1:2:6-hexanetriol and tetrakis-(2:4-pentanediono) zirconium IV; (4) N:N-dimethylcyclohexylamine, tris-(2:4-pentanediono) manganese III and ethyl cellulose and (5) tetrakis-(2:4-pentanediono) thorium IV to form intermediates containing free isocyanate groups which are foamed by reaction with N:N-dimethylcyclohexylamine (except in Example 4) and water in the presence of an octyl phenolethylene oxide reaction product and the sodium salt of sulphated methyl oleate. Specification 869,988 is referred to.ALSO:Foamed polyurethanes are made by reacting together an organic polyisocyanate and a hydroxyl ended polymer in the presence of a co-ordination compound of titanium, zirconium, hafnium, thorium or manganese with a b -diketone, b -ketoester or b -hydroxyaldehyde to give a reaction product containing free isocyanate groups which is then reacted with water. Specified co-ordinating compounds are acetylacetone, benzoylacetone, 3-cyanoacetylacetone, dibenzoylacetone, propionylacetone, trifluoroacetylacetone, methyl acetoacetate, ethyl acetoacetate, propyl acetoacetate and salicylaldehyde. Specified polyisocyanates include hexamethylene diisocyanate, tolylene diisocyanates, diphenyl methane-4 : 41-diisocyanate, 3-methyl diphenyl methane-4 : 41-diisocyanate, m- and p-phenylene diisocyanates, chlorophenylene-2:4-diisocyanate, dicyclohexylmethane diisocyanate, 2: 4 : 6-triisocyanatotoluene and 2 : 4 : 4-triisocyanatodiphenyl ether. Specified hydroxylended polymers are polyesters, polyesteramides and polyethers of which many are listed. The reaction may be continuous or discontinuous and may be effected in the presence of catalysts, non-ionic surface active agents, sodium salts of sulphuric acid derivatives of high molecular weight organic compounds, silicone oils, foam stabilising agents e.g. ethyl cellulose, certain polyhydroxy compounds e.g. trimethyl propane, plasticisers e.g. dinonyl phthalate and fire-proofing agents e.g. tri (b -chloroethyl) phosphate. The stability of the intermediate reaction products may be improved by the addition thereto of acid-reacting substances e.g. acetyl chloride. In the examples, mixed tolylene 2 : 4-and 2 : 6-diisocyanates are reacted with polypropylene glycol in the presence of: (1) tris-(2 : 4-pentanediono) manganese III; (2) tetrakis-(2 : 4-pentanediono) zirconium IV; (3) a polyether derived from propylene oxide and 1 : 2 : 6-hexane triol and tetrakis-(2 : 4- pentanediono) zirconium IV; (4) N : N-dimethyl cyclohexylamine, tris-(2 : 4-pentanediono) manganese III and ethyl cellulose and (5) tetrakis-(2 : 4-pentanediono) thorium IV which are foamed by reaction with N : N-dimethylcyclohexylamine (except in Example 4) and water in the presence of an octyl phenol-ethylene oxide reaction product and the sodium salt of sulphated methyl oleate. Specification 869,988 is referred to.
GB650659A 1959-02-25 1959-02-25 Improvements in or relating to the manufacture of foamed polyurethanes Expired GB890280A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB650659A GB890280A (en) 1959-02-25 1959-02-25 Improvements in or relating to the manufacture of foamed polyurethanes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB650659A GB890280A (en) 1959-02-25 1959-02-25 Improvements in or relating to the manufacture of foamed polyurethanes

Publications (1)

Publication Number Publication Date
GB890280A true GB890280A (en) 1962-02-28

Family

ID=9815759

Family Applications (1)

Application Number Title Priority Date Filing Date
GB650659A Expired GB890280A (en) 1959-02-25 1959-02-25 Improvements in or relating to the manufacture of foamed polyurethanes

Country Status (1)

Country Link
GB (1) GB890280A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998015585A1 (en) * 1996-10-05 1998-04-16 Tioxide Specialties Limited Catalysts
WO1998041322A1 (en) * 1997-03-19 1998-09-24 King Industries, Inc. Novel zirconium urethane catalysts
EP0960894A1 (en) * 1998-05-28 1999-12-01 Air Products And Chemicals, Inc. Group IVB metal blowing catalyst compositions for the production of polyurethane foams
WO2000002941A1 (en) * 1998-07-11 2000-01-20 Huntsman Ici Chemicals Llc Polyisocyanate compositions
EP0859805B1 (en) * 1995-11-06 2003-04-02 Huntsman International Llc Polyisocyanate composition for binding lignocellulosic material
US7485729B2 (en) 2004-08-12 2009-02-03 King Industries, Inc. Organometallic compositions and coating compositions
US8912113B2 (en) 2011-03-06 2014-12-16 King Industries, Inc. Compositions of a metal amidine complex and second compound, coating compositions comprising same

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0859805B1 (en) * 1995-11-06 2003-04-02 Huntsman International Llc Polyisocyanate composition for binding lignocellulosic material
WO1998015585A1 (en) * 1996-10-05 1998-04-16 Tioxide Specialties Limited Catalysts
WO1998041322A1 (en) * 1997-03-19 1998-09-24 King Industries, Inc. Novel zirconium urethane catalysts
US5846897A (en) * 1997-03-19 1998-12-08 King Industries, Inc. Zirconium urethane catalysts
US5965686A (en) * 1997-03-19 1999-10-12 King Industries, Inc. Zirconium urethane catalysts
EP0960894A1 (en) * 1998-05-28 1999-12-01 Air Products And Chemicals, Inc. Group IVB metal blowing catalyst compositions for the production of polyurethane foams
WO2000002941A1 (en) * 1998-07-11 2000-01-20 Huntsman Ici Chemicals Llc Polyisocyanate compositions
US7485729B2 (en) 2004-08-12 2009-02-03 King Industries, Inc. Organometallic compositions and coating compositions
US8088846B2 (en) 2004-08-12 2012-01-03 King Industries, Inc. Organometallic compositions and coating compositions
US9006316B2 (en) 2004-08-12 2015-04-14 King Industries, Inc. Organometallic compositions and coating compositions
US8912113B2 (en) 2011-03-06 2014-12-16 King Industries, Inc. Compositions of a metal amidine complex and second compound, coating compositions comprising same

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