GB795335A - Preparation of elastomeric cellular materials - Google Patents

Preparation of elastomeric cellular materials

Info

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
Application number
GB21161/56A
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.)
Goodyear Tire and Rubber Co
Original Assignee
Goodyear Tire and Rubber Co
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 Goodyear Tire and Rubber Co filed Critical Goodyear Tire and Rubber Co
Publication of GB795335A publication Critical patent/GB795335A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0061Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2483/00Characterised 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.
GB21161/56A 1955-12-21 1956-07-09 Preparation of elastomeric cellular materials Expired GB795335A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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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