GB926413A - Improvements in or relating to the manufacture of foamed polyurethane materials - Google Patents
Improvements in or relating to the manufacture of foamed polyurethane materialsInfo
- Publication number
- GB926413A GB926413A GB2783259A GB2783259A GB926413A GB 926413 A GB926413 A GB 926413A GB 2783259 A GB2783259 A GB 2783259A GB 2783259 A GB2783259 A GB 2783259A GB 926413 A GB926413 A GB 926413A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyisocyanate
- diisocyanate
- block copolymer
- prepared
- polyoxyalkylene
- 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2483/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (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 manufacture of foamed polyurethane materials by the interaction of hydroxyl group-containing polymers such as polyesters, polyesteramides and polyethers, water and organic polyisocyanate compositions comprising a major proportion by weight of a diarylmethane diisocyanate and at least 5% by weight of a polyisocyanate having more than two isocyanate groups per molecule is characterized in that the interaction is carried out in the presence of a polysiloxane-polyoxyalkylene block copolymer. The block copolymer usually has a polysiloxane block of molecular weight 500 to 2,000 and a polyoxyalkylene block of molecular weight 500 to 5,000. It can be prepared, for example, by reacting polysiloxanes having terminal ethoxy groups with polyoxyalkylene compounds having terminal hydroxyl groups. The polyisocyanate having more than two isocyanate groups may be added directly to the polyisocyanate composition or may result from (1) reaction of some of the diarylmethane diisocyanate with a polyhydric alcohol; (2) partial polymerization of the diisocyanate to isocyanurate derivatives; or (3) production of the polyisocyanate by phosgenation of a crude amine mixture containing tri- and higher derivatives. Preferably the polyisocyanate composition contains carbamyl chloride in amount to give 0,01 to 3% of ionizable chlorine. As flame-proofing agents halogen compounds, organic and inorganic phosphates and borates and oxides of antimony, tin or zinc may be added. Suitable catalysts are N-methyl morpholine, N,N-dimethylbenzylamine, b -diethylaminoethanol, triethanolamine and triethylamine and their salts with, e.g. lactic or citric acid, iron acetyl acetonate and dibutyl tin dilaurate. In examples (1) a foamed product is prepared from a mixture of a polyester of pentaerythritol, 1:3-butylene glycol, adipic acid, and phthalic anhydride (acid value 6,8 m.g. KOH/gm., OH value 7,1 m.g. KOH/gm.); water; dimethylbenzylamine lactate; b -trichlorethyl phosphate; a dimethylsiloxane/ethylene oxide/propylene oxide block copolymer; and a diphenyl methane diisocyanate composition prepared from crude diaminodiphenyl methane containing 15% poly(mainly tri-) amines; (3) a triethanolamine/propylene oxide condensate is reacted similarly. The use of a dimethylsiloxane/ethylene oxide block copolymer is also exemplified. Specifications 842,154, 848,671, 874,430 and 924,111 are referred to.ALSO:A process for the manufacture of foamed polyurethanes by the interaction of hydroxyl group-containing polymers such as polyesters, polyesteramides and polyethers, water and organic polyisocyanate compositions comprising a major proportion by weight of a diaryl methane diisocyanate and at least 5% by weight of a polyisocyanate having more than two isocyanate groups per molecule is characterised in that the interaction is carried out in the presence of a polysiloxane polyoxyalkylene block copolymer. The block copolymer usually has a polysiloxane block of molecular weight 500 to 2000 and a polyoxyalkylene block of molecular weight 500 to 5000. It can be prepared, for example, by reacting polysiloxanes having terminal ethoxy groups with polyoxyalkylene compounds having terminal hydroxyl groups. The polyisocyanates having more than two isocyanate groups may be added directly to the polyisocyanate composition or may result from (1) reaction of some of the diarylmethane diisocyanate with a polyhydric alcohol; (2) partial polymerization of the diisocyanate to isocyanurate derivatives; or (3) production of the polyisocyanate by phosgenation of a crude amine mixture. Preferably the composition contains corbamyl chloride in amount to give 0,01% to 3% of ionisable chlorine. As flame-proofing agents there may be added halogen compounds, organic and inorganic phosphates and borates, and oxides of antimony, tin or zinc. Suitable catalysts methyl morpholine, dimethyl benzylamine, diethylaminoethanol, triethanolamine and triethylamine and their salts with e.g. lactic or citric acid, iron acetyl acetonate, and dibutyl tin dilaurate. In examples (1) a foamed product is prepared from a mixture of a polyester of pentaerythritol, 1 : 3- butylene glycol, adipic acid and phthalic anhydride (acid value 6,8 m.g. KOH and OH value 7,1 m.g. KOH (g.m.); water; dimethylbenzylamine lactate; trib - chlorethyl phosphate; a dimethyl siloxane/ethylene oxide/propylene oxide block copolymer; a diphenylmethane diisocyanate composition prepared from crude diaminodiphenyl methane containing 15% poly (mainly tri-) amines; (3) a triethanolamine/propylene oxide condensate is reacted similarly. Specifications 842,154, 848,671, 874,430 and 924,111 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2783259A GB926413A (en) | 1959-08-14 | 1959-08-14 | Improvements in or relating to the manufacture of foamed polyurethane materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2783259A GB926413A (en) | 1959-08-14 | 1959-08-14 | Improvements in or relating to the manufacture of foamed polyurethane materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB926413A true GB926413A (en) | 1963-05-15 |
Family
ID=10266030
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2783259A Expired GB926413A (en) | 1959-08-14 | 1959-08-14 | Improvements in or relating to the manufacture of foamed polyurethane materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB926413A (en) |
-
1959
- 1959-08-14 GB GB2783259A patent/GB926413A/en not_active Expired
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