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GB1005852A - Foamed polyurethanes - Google Patents

Foamed polyurethanes

Info

Publication number
GB1005852A
GB1005852A GB5525/62A GB552562A GB1005852A GB 1005852 A GB1005852 A GB 1005852A GB 5525/62 A GB5525/62 A GB 5525/62A GB 552562 A GB552562 A GB 552562A GB 1005852 A GB1005852 A GB 1005852A
Authority
GB
United Kingdom
Prior art keywords
diisocyanate
water
tolylene
diisocyanates
prepared
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
GB5525/62A
Inventor
Dennis Charlton Allport
Herbert Gudgeon
John Francis Wood
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB5525/62A priority Critical patent/GB1005852A/en
Publication of GB1005852A publication Critical patent/GB1005852A/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
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4244Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups
    • C08G18/4247Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids
    • C08G18/4252Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids derived from polyols containing polyether groups and polycarboxylic 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
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/487Polyethers containing cyclic groups
    • C08G18/4879Polyethers containing cyclic groups 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
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4887Polyethers containing carboxylic ester groups derived from carboxylic acids other than acids of higher fatty oils or other than resin 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
    • C08G2110/00Foam properties
    • C08G2110/0008Foam properties flexible
    • 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
    • C08G2110/0033Foam properties having integral skins

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 foamed polyurethane is produced by interacting an organic polyisocyanate with water and a polyether containing at least 2 hydroxyl groups per molecule which is the reaction product of a polyalkylene glycol and an aromatic polycarboxylic acid having at least 3 carboxyl groups per molecule or its ester, chloride or anhydride. The polyether may be prepared at an elevated temperature under an inert atmosphere and in the presence of a catalyst, e.g. tetrabutyl-orthotitinate. The number of hydroxyl groups present per carboxyl group may be 0.01-0.6 for tricarboxylic acids and 0.01-0.5 for tetra-carboxylic acids. Specified acid are trimellitic, trimeric and pyromellitic. Mixtures may be used. Specified polyalkylene glycols may be prepared from one or more cyclic oxides, e.g. ethylene, propylene or butylene oxides, tetrahydrofuran or oxacyclobutane, using a catalyst, e.g. KOH, in the presence of an initiator having two active hydrogen atoms, e.g. water or diethylene glycol. Polyisocyanates specified for polyurethane formation are: hexamethylene diisocyanate, tolylene-2,4 and 2,6-diisocyanates, diphenylmethane - 4,41 - diisocyanate, 3 - methyldiphenylmethane - 4,41 - diisocyanate, m- and p-phenylene diisocyanates, chlorophenylene - 2,4 - diisocyanate, dicyclohexylmethane diisocyanate, 2,4,6-triisocyanatotoluene, 2,4,41 - triisocyanatodiphenyl ether and isocyanurate trimers and uretdione dimers of tolylene - 2,4 and 2,6 - diisocyanates. Mixtures of isocyanates may be used. 1-10% water is used. Other additives may be: catalysts, e.g. tertiary amines, iron and manganese acetylacetonates, dibutyltin dilaurate, and stannous octoate; surface-active agents, e.g. oxyethylated phenols and fatty alcohols, sulphonated methyl oleate, alkyl and aryl polysiloxanes and siloxane-oxy-alkylene copolymers, flame retardants, e.g. tri-b -chloroethyl phosphate and antimony oxide, plasticizers, e.g. tricresyl phosphate and dioctyl phthalate, colouring, fillers, e.g. carbon black, and silica, colour stabilizers, whitening agents and antioxidants, e.g. tert-butyl catechol and sterically hindered phenols. In Example (1) a polyether prepared by interacting polypropylene glycol and trimellitic acid under nitrogen in the presence of tetraorthobutyl titinate, was treated with water and tolylene-2,4 and 2,6-diisocyanate in the presence of 4-dimethylaminopyridine, dimethylbenzylamine, stannous octoate and a siloxane-oxyalkylene block copolymer. The reactants were allowed to foam in a mould. In Example (2) the carboxyl derivative used was pyromellitic dianhydride.
GB5525/62A 1962-02-13 1962-02-13 Foamed polyurethanes Expired GB1005852A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB5525/62A GB1005852A (en) 1962-02-13 1962-02-13 Foamed polyurethanes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5525/62A GB1005852A (en) 1962-02-13 1962-02-13 Foamed polyurethanes

Publications (1)

Publication Number Publication Date
GB1005852A true GB1005852A (en) 1965-09-29

Family

ID=9797836

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5525/62A Expired GB1005852A (en) 1962-02-13 1962-02-13 Foamed polyurethanes

Country Status (1)

Country Link
GB (1) GB1005852A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0141901A2 (en) * 1983-06-06 1985-05-22 Union Carbide Corporation Adducts and polymer-polyols useful in the preparation of improved plastics, including polyurethane foams, elastomers
EP0527613A2 (en) * 1991-08-08 1993-02-17 Huntsman Corporation Preparation of foams using polyfunctional organic acids
CN111961179A (en) * 2020-08-27 2020-11-20 张家港长泰汽车饰件材料有限公司 Efficient flame-retardant polyurethane foam and preparation method and application thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0141901A2 (en) * 1983-06-06 1985-05-22 Union Carbide Corporation Adducts and polymer-polyols useful in the preparation of improved plastics, including polyurethane foams, elastomers
EP0141901A3 (en) * 1983-06-06 1985-08-07 Union Carbide Corporation Adducts and polymer-polyols useful in the preparation of improved plastics, including polyurethane foams, elastomers
EP0527613A2 (en) * 1991-08-08 1993-02-17 Huntsman Corporation Preparation of foams using polyfunctional organic acids
EP0527613A3 (en) * 1991-08-08 1993-04-21 Huntsman Corporation Preparation of foams using polyfunctional organic acids
CN111961179A (en) * 2020-08-27 2020-11-20 张家港长泰汽车饰件材料有限公司 Efficient flame-retardant polyurethane foam and preparation method and application thereof

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