GB990633A - Improvements in or relating to the manufacture of polymers - Google Patents

Improvements in or relating to the manufacture of polymers

Info

Publication number
GB990633A
GB990633A GB804961A GB804961A GB990633A GB 990633 A GB990633 A GB 990633A GB 804961 A GB804961 A GB 804961A GB 804961 A GB804961 A GB 804961A GB 990633 A GB990633 A GB 990633A
Authority
GB
United Kingdom
Prior art keywords
tertiary amine
hetero atoms
zinc salt
lead acetate
reaction mixture
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
GB804961A
Inventor
Harry James Twitchett
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 GB804961A priority Critical patent/GB990633A/en
Publication of GB990633A publication Critical patent/GB990633A/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
    • 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
    • C08G18/161Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
    • C08G18/163Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22 covered by C08G18/18 and C08G18/22

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 manufacture of polyurethanes by the reaction of organic polyisocyanates with hydroxyl group-containing polymers containing at least two isocyanate reactive groups per molecule is characterized in that it is carried out in the presence of a zinc salt of an acid of the formula <FORM:0990633/C3/1> wherein R and R1 are the same or different hydrocarbon or substituted hydrocarbon radicals which may be higher alkyl, cycloalkyl, aryl, aralkyl or an alkyl radical interrupted by one or more hetero atoms such as O or S, or wherein R and R1 may together form an alkylene group, optionally interrupted by hetero atoms such as O or S, which together with the remainder of the thio-acid molecule forms a ring structure containing 4 to 8 atoms, and wherein X is oxygen or sulphur, and also in the presence of a tertiary amine. The tertiary amine may be used wholly or partly in the form of a coordination complex with the zinc salt and the complex may be prepared in situ in the reaction mixture. Water and/or low boiling point liquids may be added to the reaction mixture to give foamed products. The hydroxyl groupcontaining polymer may be a polyester, polyesteramide or polyether or a mixture thereof. Many zinc salts, tertiary amines, complexes of zinc salts and tertiary amines, starting materials for the preparation of hydroxyl group-containing polymers, organic polyisocyanates and low boiling liquids are specified. Other additives which may be present in the reaction mixture are surface-active agents such as oxyethylated phenols, oleyl alcohol, sulphated methyl oleate, polyalkylsiloxanes and block copolymers thereof with polyalkylene oxides; flame retardants such as b -trichloroethyl phosphate and antimony oxide; plasticizers such as tricresyl phosphate and dioctyl phthalate; colouring matters and fillers, such as carbon black and silica; antioxidants such as t-butylcatechol; other types of catalysts such as iron and manganese acetylacetonates, dibutyltin dilaurate, stannous octoate, lead acetate, basic lead acetate and lead 2-ethylhexoate; and solvents such as methyl ethyl ketone and cyclohexanone. Examples describe the preparation of polyurethane foams and a lacquer. Specifications 937,882 and 990,634 are referred to.ALSO:Polyurethanes are prepared in the presence, as catalyst, of a mixture of a zinc salt of an acid of the formula <FORM:0990633/B1-B2/1> wherein R and R1 are hydrocarbon or substituted hydrocarbon radicals which may be higher alkyl, cycloalkyl, aryl, aralkyl or an alkyl radical interrupted by one or more hetero atoms such as O or S, or wherein R and R1 may together form an alkylene group optionally interrupted by hetero atoms such as O or S, and a tertiary amine. The tertiary amine may be present wholly or in part as a complex with the zinc salt. Mixtures of compounds may be used and other catalysts such as iron and manganese acetylacetonates, dibutyltindilaurate, stannous octoate, lead acetate, basic lead acetate and lead 2-ethylhexoate may also be present. Specifications 937,882 and 990,634 are referred to.
GB804961A 1961-03-06 1961-03-06 Improvements in or relating to the manufacture of polymers Expired GB990633A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB804961A GB990633A (en) 1961-03-06 1961-03-06 Improvements in or relating to the manufacture of polymers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB804961A GB990633A (en) 1961-03-06 1961-03-06 Improvements in or relating to the manufacture of polymers

Publications (1)

Publication Number Publication Date
GB990633A true GB990633A (en) 1965-04-28

Family

ID=9844802

Family Applications (1)

Application Number Title Priority Date Filing Date
GB804961A Expired GB990633A (en) 1961-03-06 1961-03-06 Improvements in or relating to the manufacture of polymers

Country Status (1)

Country Link
GB (1) GB990633A (en)

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