GB890280A - Improvements in or relating to the manufacture of foamed polyurethanes - Google Patents
Improvements in or relating to the manufacture of foamed polyurethanesInfo
- 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
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
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/222—Catalysts 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.
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)
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 |
-
1959
- 1959-02-25 GB GB650659A patent/GB890280A/en not_active Expired
Cited By (11)
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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