GB866324A - Preparation of cellular polyurethane - Google Patents
Preparation of cellular polyurethaneInfo
- Publication number
- GB866324A GB866324A GB41358/58A GB4135858A GB866324A GB 866324 A GB866324 A GB 866324A GB 41358/58 A GB41358/58 A GB 41358/58A GB 4135858 A GB4135858 A GB 4135858A GB 866324 A GB866324 A GB 866324A
- Authority
- GB
- United Kingdom
- Prior art keywords
- usual ones
- silanol
- compounds
- tetra
- products
- 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
- C08J2375/08—Polyurethanes from polyethers
-
- 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
Cellular polyurethanes are obtained by reacting a polyalkylene ether of Mol. wt. at least 400 and having terminal -OH and/or -NH2, water, an organic polyisocyanate, and an organo silicon compound having at least one hydroxyl group. Suitable organosilicon compounds are silanols and siloxanes having one or more -OH, e.g. diethyl- and diphenyl-silanediol; triphenyl silanol; tetramethyl, tetraethyl and tetraphenyl disiloxanediol; or an ester formed from a silanol or a siloxane and adipic or succinic acid. The polyethers described are the usual ones (but include polythioethers) together with the poly addition products of polyacetals and olefines of the type disclosed in Specification 866,323. They may be used in conjunction with other polyfunctional compounds. The polyisocyanates are the usual ones, and they may contain chlorine, nitro or alkoxy substituents. The trimerized products of monomeric diisocyanates and the reaction product of a polyol with a diisocyanate can also be used. A prepolymer may be formed, or not, as desired. A tertiary amine catalyst may be used. Specifications 769,680 and 769,682 also are referred to.ALSO:Cellular polyurethanes are obtained by reacting a polyalkylene ether of Mol-wt. at least 400 and having terminal-OH and/or -NH2, water, an organic polyisocyanate, and an organo silicon compound having at least one hydroxyl group. Suitable organasilicon compounds are silanols and siloxanes having one or more -OH, e.g. diethyl- and diphenyl-silane diol; triphenyl sil anol; tetra methyl, tetra ethyl-and tetra phenyl-disiloxane diol; or an ester formed from a silanol or a siloxane and adipic or succinic acid. The polyethers described are the usual ones (but include also polythioethers) together with the poly addition products of polyacetals and olefines of the type disclosed in Specification 866,323. They may be used in conjunction with other polyfunctional compounds. The polyisocyanates are the usual ones, and they may contain chlorine, nitro or alkoxy substituents. The trimerized products of monomeric diisocyanates and the reaction product of a polyol with a diisocyanate can also be used. The process may give a prepolymer, or not, as desired. A tertiary amine catalyst may be used. Specifications 769,680 and 769,682 also are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE866324X | 1957-12-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB866324A true GB866324A (en) | 1961-04-26 |
Family
ID=6801996
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB41358/58A Expired GB866324A (en) | 1957-12-31 | 1958-12-22 | Preparation of cellular polyurethane |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB866324A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3399247A (en) * | 1957-12-31 | 1968-08-27 | Bayer Ag | Preparation of cellular polyurethane |
-
1958
- 1958-12-22 GB GB41358/58A patent/GB866324A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3399247A (en) * | 1957-12-31 | 1968-08-27 | Bayer Ag | Preparation of cellular polyurethane |
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