GB1004924A - Improved polyurethane foam and method of making it - Google Patents

Improved polyurethane foam and method of making it

Info

Publication number
GB1004924A
GB1004924A GB2514062A GB2514062A GB1004924A GB 1004924 A GB1004924 A GB 1004924A GB 2514062 A GB2514062 A GB 2514062A GB 2514062 A GB2514062 A GB 2514062A GB 1004924 A GB1004924 A GB 1004924A
Authority
GB
United Kingdom
Prior art keywords
mixture
molecular weight
weight
diisocyanates
parts
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
GB2514062A
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.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn 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 Upjohn Co filed Critical Upjohn Co
Publication of GB1004924A publication Critical patent/GB1004924A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups

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

A polyurethane foam is produced by reacting in the presence of a blowing agent a branched active hydrogen-containing synthetic resin (A) having not less than three active hydrogen containing groups to the molecule with a combined hydroxyl-acid number of at least 225, at least 75% of the active hydrogen groups being alcoholic hydroxyl groups, and an amount at least sufficient to react with all the said hydroxyl groups of a mixture (B) of methylene bridged polyphenyl polyisocyanates comprising diisocyanates, triisocyanates, and higher molecular weight polyisocyanates, substantially 45 to 60 parts per 100 parts by weight of said mixture being diisocyanates, the combined weight of diisocyanates and triisocyanates being substantially 60 to 75 parts per 100 parts by weight of said mixture, the remainder of the mixture having a sufficiently high average molecular weight that the average molecular weight of the total mixture is at least 381, said mixture having vixcosity less than or equal to 1090 centipoises at 25 DEG C. and an isocyanate equivalent of at least 127, said mixture of isocyanates having been formed by phosgenation of diamines, triamines and higher molecular weight polyamines formed by acid condensation of aniline and formaldehyde. The active hydrogen-containing material (A) may be a polyether, polyester or polyesteramide, many such materials are specified. In a typical Example (1) a polyesteramide derived from polymerized linoleic acid by reaction with polyamines and a trimethylol propane adipate polyester was reacted with the mixture of polyisocyanates in the presence of water and N-methyl morpholine to produce a polyurethane foam.ALSO:A mixture of methylene bridged polyphenyl polyisocyanates comprising diisocyanates, triisocyanates and higher molecular weight polyisocyanates, substantially 45 to 60 parts per 100 parts by weight of said mixture being diisocyanates, the combined weight of diisocyanates and triisocyanates being substantially 60 to 75 parts per 100 parts by weight of said mixture, the remainder of said mixture having a sufficiently high average molecular weight that the average molecular weight of the total mixture is at least 381, said mixture having a viscosity less than or equal t2 1090 centipoises at 25 DEG C. and an isocyanate equivalent of at least 127; is formed by phosgenation of diamines, triamines and higher molecular weight polyamines formed by acid condensation of aniline and formaldehyde.
GB2514062A 1961-06-29 1962-06-29 Improved polyurethane foam and method of making it Expired GB1004924A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12052461A 1961-06-29 1961-06-29

Publications (1)

Publication Number Publication Date
GB1004924A true GB1004924A (en) 1965-09-22

Family

ID=22390842

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2514062A Expired GB1004924A (en) 1961-06-29 1962-06-29 Improved polyurethane foam and method of making it

Country Status (4)

Country Link
BE (1) BE641748A (en)
DE (1) DE1248925B (en)
GB (1) GB1004924A (en)
NL (2) NL280353A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4272618A (en) * 1979-04-30 1981-06-09 Texaco Development Corp. Heat stable reaction injection molded elastomers
EP0151401A2 (en) * 1984-01-24 1985-08-14 Bayer Ag Rigid flame retardant polyurethane foams having closed cells

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4272618A (en) * 1979-04-30 1981-06-09 Texaco Development Corp. Heat stable reaction injection molded elastomers
EP0151401A2 (en) * 1984-01-24 1985-08-14 Bayer Ag Rigid flame retardant polyurethane foams having closed cells
EP0151401A3 (en) * 1984-01-24 1987-03-18 Bayer Ag Rigid flame retardant polyurethane foams having closed cells

Also Published As

Publication number Publication date
BE641748A (en)
NL280353A (en)
NL128617C (en)
DE1248925B (en) 1967-08-31

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