GB909358A - Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds - Google Patents

Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds

Info

Publication number
GB909358A
GB909358A GB1923860A GB1923860A GB909358A GB 909358 A GB909358 A GB 909358A GB 1923860 A GB1923860 A GB 1923860A GB 1923860 A GB1923860 A GB 1923860A GB 909358 A GB909358 A GB 909358A
Authority
GB
United Kingdom
Prior art keywords
reaction
compounds
carboxylic acids
acid
include those
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
GB1923860A
Inventor
James Harry Wild
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 GB1923860A priority Critical patent/GB909358A/en
Publication of GB909358A publication Critical patent/GB909358A/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
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/22Catalysts containing metal compounds
    • C08G18/222Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26

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)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A process for the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds is characterized in that the reaction is carried out in the presence of a mercury salt of a carboxylic acid. Salts listed include those of monocarboxylic acids; dimethylglycine or 6-dimethylaminocaproic acid; di- or tri-carboxylic acids such as the reaction products of polyoxyalkylene diols or triols with two or three molecular proportions, respectively, of maleic or succinic anhydride; N,N1-ethylenediamine tetracarboxylic acid; carboxylic acids containing aromatic nuclei; and cycloaliphatic carboxylic acids. Polyesters, polyesteramides, polyethers and mixtures thereof are suitable hydroxy compounds. The polyethers include those obtained from cyclic oxides having a functionality greater than two. The mercury salts can be used together with tertiary amine catalysts, soluble organic compounds of metals such as iron or manganese acetylacetonate antimony compounds, or dibutyl tin dilaurate or stannous octoate. The reaction mixture may also contain antioxidants, such as tert. butyl catechol, surface-active agents, flame-retardants such as trichloroethyl phosphate and antimony oxide, plasticizers such as tricresyl phosphate and dioctyl phthalate and carbon black, silica, colour stabilizers and whitening agents. The examples describe the preparation of cellular products.ALSO:A process for the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds is characterised in that the reaction is carried out in the presence of a mercury salt of a carboxylic acid. The process is applicable to the preparation of cellular products, in one preferred embodiment by the simultaneous interaction of a secondary hydroxyl-ended polymer, especially a polyether, an organic polyisocyanate and water and/or a low boiling liquid in the presence of the mercury salt. Salts listed include those of monocarboxylic acids; dimethylglycine or 6-dimethylaminocaproic acid; di-or tri-carboxylic acids such as the reaction products of polyoxyalkylene diols or triols with two or three molecular proportions, respectively, of maleic or succinic anhydride; N, N1-ethylenediamine-tetracarboxylic acid; carboxylic acids containing aromatic nuclei; and cycloaliphatic carboxylic acids. Polyesters, polyester amides, polyethers and mixtures thereof are suitable hydroxy compounds. The polyethers include those obtained from cyclic oxides having a functionality greater than two. The tin salts can be used together with tertiary amine catalysts, soluble organic compounds of metals such as iron or manganese acetyl-acetonate, antimony compounds or dibutyl tin dilaurate or stannous octoate. The reaction mixture may also contain antioxidants such as tert butyl catechol, surface-active agents, flame retardants such as trichlorethyl phosphate and antimony oxide, plasticizers such as tricresyl phosphate and dioctyl phthalate, and carbon black, silica, colour stabilizers and whitening agents. In a typical example, (4) a mixture polypropylene glycol and oxypropylated trimethylolpropane, blended together with triethylene diamine, N-dimethylbenzylamine, mercury salt of octoic acid, alkylsilane-polyoxyalkylene block copolymer and water, is converted to a cellular product by blending with tolylene -2 : 4-and 2 : 6-diisocyanates. In other examples the salt used is the 2-ethylhexoate.
GB1923860A 1960-05-31 1960-05-31 Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds Expired GB909358A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1923860A GB909358A (en) 1960-05-31 1960-05-31 Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1923860A GB909358A (en) 1960-05-31 1960-05-31 Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds

Publications (1)

Publication Number Publication Date
GB909358A true GB909358A (en) 1962-10-31

Family

ID=10126009

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1923860A Expired GB909358A (en) 1960-05-31 1960-05-31 Improvements in or relating to the manufacture of polymeric materials by the reaction of organic isocyanates with hydroxyl group-containing compounds

Country Status (1)

Country Link
GB (1) GB909358A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3395108A (en) * 1964-09-30 1968-07-30 Allied Chem Manufacture of filled urethane elastomers cured with a mixture of polyol, inert fille, mercuric salt of an aliphatic monocarboxylic acid and a basic metal compound
US3419509A (en) * 1965-11-22 1968-12-31 Wyandotte Chemicals Corp Mercury compounds as catalysts for the polyurethane reaction
US3492255A (en) * 1966-07-07 1970-01-27 Allied Chem Noncellular rapidly gelled polyurethane compositions
US3670070A (en) * 1968-12-17 1972-06-13 Usm Corp Processes for molding polyurethane foam articles
GB2133413A (en) * 1982-12-20 1984-07-25 Basf Wyandotte Corp Preparation of noncellular polyurethane elastomers
US5064871A (en) * 1989-07-19 1991-11-12 Essex Specialty Products, Inc. Latent catalysts comprising bismuth carboxylates and zirconium carboxylates

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3395108A (en) * 1964-09-30 1968-07-30 Allied Chem Manufacture of filled urethane elastomers cured with a mixture of polyol, inert fille, mercuric salt of an aliphatic monocarboxylic acid and a basic metal compound
US3419509A (en) * 1965-11-22 1968-12-31 Wyandotte Chemicals Corp Mercury compounds as catalysts for the polyurethane reaction
US3492255A (en) * 1966-07-07 1970-01-27 Allied Chem Noncellular rapidly gelled polyurethane compositions
US3670070A (en) * 1968-12-17 1972-06-13 Usm Corp Processes for molding polyurethane foam articles
GB2133413A (en) * 1982-12-20 1984-07-25 Basf Wyandotte Corp Preparation of noncellular polyurethane elastomers
US5064871A (en) * 1989-07-19 1991-11-12 Essex Specialty Products, Inc. Latent catalysts comprising bismuth carboxylates and zirconium carboxylates

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