GB795335A - Preparation of elastomeric cellular materials - Google Patents
Preparation of elastomeric cellular materialsInfo
- Publication number
- GB795335A GB795335A GB21161/56A GB2116156A GB795335A GB 795335 A GB795335 A GB 795335A GB 21161/56 A GB21161/56 A GB 21161/56A GB 2116156 A GB2116156 A GB 2116156A GB 795335 A GB795335 A GB 795335A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyester
- silicone oil
- mixture
- polyisocyanate
- phenylene
- 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
In the preparation of an elastomeric cellular material by reacting a polymeric material containing a plurality of active hydrogen atoms, a polyisocyanate and water, from 0.002 to 0.02 per cent of a silicone oil is added to the reaction mixture. When cushions are made from this material there is thus less movement of the upper part of the cushion parallel to the lower part when a horizontal force is applied. The polymeric material may be a linear or branched polyester or polyesteramide or a polyalkylene ether glycol. The polyisocyanate may be p-phenylene, m-phenylene, 1.5-naphthalene, 4.41-diphenylenemethane, tolyene or hexamethylene diisocyanate. The silicone oil has the formula: <FORM:0795335/IV (a)/1> wherein R is an organic hydrocarbon radical (e.g. methyl or ethyl). In Examples (2)-(5), to a prepolymer made by heating a polyester derived from adipic acid, ethylene glycol, diethylene glycol and 1.4-butanediol with tolylene diisocyanate there was added first tolylenediisocyanate and castor oil, then an activator mixture comprising the above polyester, water, N-methylmorpholine an alkylated aryl polyether alcohol (as emulsifier) and a condensate of 4 mols. of butyraldehyde and 1 mol. of aniline, and finally a silicone oil; the complete reaction mixture was then poured into a mould where it was permitted to expand and cure and was then heated to complete the cure; (7), (8) and (9), similar to Examples 2-5, except that the prepolymer is prepared by heating a mixture of the polyester, the tolylene diisocyanate and 1.4-butane diol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US795335XA | 1955-12-21 | 1955-12-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB795335A true GB795335A (en) | 1958-05-21 |
Family
ID=22151149
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB21161/56A Expired GB795335A (en) | 1955-12-21 | 1956-07-09 | Preparation of elastomeric cellular materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB795335A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3036021A (en) * | 1958-11-14 | 1962-05-22 | Bayer Ag | Preparation of polyurethane plastics |
US4306035A (en) * | 1980-05-30 | 1981-12-15 | Union Carbide Corporation | Use of alkoxysilicon compositions as foam stabilizers in high resilience polyurethane foams |
-
1956
- 1956-07-09 GB GB21161/56A patent/GB795335A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3036021A (en) * | 1958-11-14 | 1962-05-22 | Bayer Ag | Preparation of polyurethane plastics |
US4306035A (en) * | 1980-05-30 | 1981-12-15 | Union Carbide Corporation | Use of alkoxysilicon compositions as foam stabilizers in high resilience polyurethane foams |
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