GB939465A - Polyurethane foam - Google Patents

Polyurethane foam

Info

Publication number
GB939465A
GB939465A GB7180/62A GB718062A GB939465A GB 939465 A GB939465 A GB 939465A GB 7180/62 A GB7180/62 A GB 7180/62A GB 718062 A GB718062 A GB 718062A GB 939465 A GB939465 A GB 939465A
Authority
GB
United Kingdom
Prior art keywords
polyol
mixture
tall oil
trichlorofluoromethane
listed
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
GB7180/62A
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.)
Bayer Corp
Original Assignee
Mobay Corp
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 Mobay Corp filed Critical Mobay Corp
Publication of GB939465A publication Critical patent/GB939465A/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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/36Hydroxylated esters of higher fatty acids
    • 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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3271Hydroxyamines
    • C08G18/3278Hydroxyamines containing at least three hydroxy groups
    • 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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3271Hydroxyamines
    • C08G18/329Hydroxyamines containing aromatic groups
    • 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
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/675Low-molecular-weight compounds
    • C08G18/6765Low-molecular-weight compounds containing the unsaturation at least partially in a cyclic ring having at least one oxygen atom in the ring
    • 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
    • C08G2110/00Foam properties
    • C08G2110/0025Foam properties rigid
    • 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
    • C08G2110/00Foam properties
    • C08G2110/0041Foam properties having specified density
    • C08G2110/005< 50kg/m3
    • 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
    • C08G2110/00Foam properties
    • C08G2110/0083Foam properties prepared using water as the sole blowing agent

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 process for the production of a substantially rigid polyurethane foam having predominantly closed pores comprises reacting an organic polyisocyanate, a polyol having a molecular weight of from 100 to 600 and containing at least one tertiary nitrogen atom and at least three hydroxyl groups, and tall oil (the amount of tall oil in the resulting mixture calculated on the combined weight of the polyol and the tall oil being from 30% by weight to 90% by weight) and simultaneously or subsequently foaming the reaction mixture by means of a blowing agent. Suitable polyisocyanates are listed, and include crude 4,41-diphenylmethane diisocyanate and crude 2,4- or 2,6-toluene diisocyanates which contain hydrolysable chlorine, such materials giving products of greater dimensional stability. A mixture of di- and tri-isocyanates can be used. The polyol containing tertiary nitrogen can be obtained by condensing a polyamine with an alkylene oxide. A number of aliphatic, aromatic and heterocyclic polyamines are listed. The aromatic compounds may contain alkyl, alkoxy, nitro or hydroxyalkylene substituents. A diamine which contains one primary and one secondary amino group can also be used. Hydroxy poly(alkylene thioether) derivatives are also suitable starting materials. Blowing of the products can result from the presence in the reaction mixture of water, an inert gas such as air, nitrogen, carbon dioxide or argon, or trichlorofluoromethane or other chlorofluoroalkane, or pentane or hexane. One shot or prepolymer methods can be used. As catalysts tin compounds and tertiary amines are listed. A silane oxyalkylene block copolymer is also preferably present in the reaction mixture. In Example (1) there are mixed tall oil and N,N,N1,N1-tetrakis-(2-hydroxypropyl) ethylene diamine, and then, using the apparatus of Specification 769,682, there are mixed in crude 4,41-diphenylmethane diisocyanate containing hydrolysable chloride, a silicone oil, and trichlorofluoromethane. The mixture is discharged into a cavity and rises and sets to a rigid foam. In other generally similar Examples (2) to (5) the polyol is a propylene oxide/tolylene diamine condensate and there are used as catalysts a mixture of 1-methyl-4-dimethylaminoethyl-piperazine and stannous octoate. In Example (5) water replaces trichlorofluoromethane as blowing agent. Specifications 769,680, 804,369 and 939,464 also are referred to.ALSO:A process for the production of a substantially rigid polyurethane foam having predominantly closed pores comprises reacting an organic polyisocyanate, a polyol having a molecular of from 100 to 600 and containing at least one tertiary nitrogen atom and at least three hydroxyl groups, and tall oil (the amount of tall oil in the resulting mixture calculated on the combined weight of the polyol and the tall oil being from 30% by weight to 90% by weight) and simultaneously or subsequently foaming the reaction mixture by means of a blowing agent. Suitable polyisocyanates are listed, and include crude 4, 41- diphenyl-methane diisocyanate and crude 2, 4- or 2, 6-toluene diisocyanates which contain hydrolysable chlorine, such materials giving products of greater dimensional stability. A mixture of di- and triisocyanates can be used. The polyol containing tertiary nitrogen can be obtained by condensing a polyamine with an alkylene oxide. A number of aliphatic, aromatic and heterocyclic polyamines are listed. The aromatic compounds may contain alkyl, alkoxy, nitor or hydroxyalkylene substituents. A diamine which contains one primary and one secondary amino group can also be used. Hydroxy poly(alkylene thioether) derivatives are also suitable starting materials. Blowing of the products can result from the presence in the reaction mixture of water, an inert gas such as air, nitrogen, carbon dioxide or argon, or trichlorofluoromethane or other chlorofluoroalkane, or pentane or hexane. One-shot or prepolymer methods can be used. As catalysts tin compounds and tertiary amines are listed. A silane oxyalkylene block copolymer is also preferably present in the reaction mixture. In Example (1) there are mixed tall oil and N, N, N1, N1- tetrakis(3-hydroxypropyl)ethylene diamine, and then, using the apparatus described in Specification 769,682, there are mixed in crude 4, 41-diphenylmethane diisocyanate containing hydrolysable chloride, a silicone oil, and trichlorofluoromethane. The mixture is discharged into a cavity and rises and sets to a rigid foam. In other, generally similar Examples (2) to (5) the polyol is a propylene oxide/tolylene diamine condensate and there are used as catalysts a mixture of 1-methyl-4 dimethyl-aminoethyl-piperazine and stannous octoate. In Example (5) water replaces trichlorofluoromethane as blowing agent. Specifications 769,680, 804,369 and 939,464 also are referred to.
GB7180/62A 1961-02-23 1962-02-23 Polyurethane foam Expired GB939465A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9090961A 1961-02-23 1961-02-23

Publications (1)

Publication Number Publication Date
GB939465A true GB939465A (en) 1963-10-16

Family

ID=22224911

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7180/62A Expired GB939465A (en) 1961-02-23 1962-02-23 Polyurethane foam

Country Status (3)

Country Link
BE (1) BE614134A (en)
DE (1) DE1160613B (en)
GB (1) GB939465A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI77676C (en) * 1986-01-22 1989-04-10 Lohja Ab Oy FOERFARANDE FOER FRAMSTAELLNING AV ETT ISOCYANURATMODIFIERAT POLYURETANSKUM OCH MEDELST FOERFARANDET FRAMSTAELLT POLYURETANSKUM.
CN113214731A (en) * 2021-04-26 2021-08-06 中科院广州化灌工程有限公司 Durable plant oil-based anti-graffiti easy-to-clean coating and preparation method and application thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT699971A (en) * 1958-08-15

Also Published As

Publication number Publication date
DE1160613B (en) 1964-01-02
BE614134A (en) 1962-06-18

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