GB971974A - Manufacture of polyurethanes - Google Patents

Manufacture of polyurethanes

Info

Publication number
GB971974A
GB971974A GB3870961A GB3870961A GB971974A GB 971974 A GB971974 A GB 971974A GB 3870961 A GB3870961 A GB 3870961A GB 3870961 A GB3870961 A GB 3870961A GB 971974 A GB971974 A GB 971974A
Authority
GB
United Kingdom
Prior art keywords
dimethylol
production
specified
alkylene oxides
polyurethanes
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
GB3870961A
Inventor
David Hay Coffey
Frank Whitley Lord
Reginald John William Reynolds
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 GB3870961A priority Critical patent/GB971974A/en
Publication of GB971974A publication Critical patent/GB971974A/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
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/6505Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen the low-molecular compounds being compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6511Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen the low-molecular compounds being compounds of group C08G18/32 or polyamines of C08G18/38 compounds of group C08G18/3203
    • 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
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step

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

Polyurethanes are produced by the reaction of organic polyisocyanates, hydroxyl group-containing polymers having at least two isocyanate reactive groups per molecule and, at the same time or subsequently a phenol having at least two methylol groups attached to phenolic aromatic rings but not more than two methylol groups on any one phenolic aromatic ring. Suitable phenols specified are dimethylol-p-cresol; dimethylol-o-cresol; 2-chloro-4, 6-dimethylolphenol; 3, 31, 5, 51-tetramethylol-4, 41-dihydroxydiphenylpropane; dimethylol-p-t-butylphenol and dimethylol-p-nonylphenol. The hydroxyl group containing polymers may be linear or branched chain, saturated or unsaturated polyesters or polyesteramides for the production of which many starting materials are specified, or they may be hydroxyl terminated polyethers which are the polymerization or copolymerization products of alkylene oxides which may be initiated by a glycol or a primary monoamine, or they may be branched chain polyethers prepared by polymerizing alkylene oxides in the presence of polyhydric compounds e.g. polyhydric alcohols, alkanolamines, sucrose, phenolformaldehyde reaction products, polyamines, glycidol, 3-hydroxymethylcyclooxabutanes and diepoxides. Many organic polyisocyanates are specified including di-isocyanates, tri-isocyanates, reaction products of an excess of a di-isocyanate with a polyhydric alcohol, uretedione dimers and isocyanurate polymers. The process of the invention is useful in the production of polyurethane coatings and foams. In the production of the latter blowing may be by means of water or a volatile liquid many of which are specified. Water may also be used as a chain extender for the polyurethanes of the invention preferably by using the process of Specification 926,971. Other additives which may be present are surface active agents e.g. oxyethylated phenols, fatty alcohols such as oleyl alcohol, or sulphated methyl oleate, polyalkylsiloxanes and block copolymers thereof with alkylene oxides; flame retardants e.g. b -trichloroethyl phosphate and antimony oxide; plasticizers e.g. tricresyl phosphate and dioctyl phthalate; pigments and fillers e.g. carbon black and silica, antioxidants e.g. t-butylcatechol and sterically hindered phenols; solvents e.g. acetone, cyclohexanone, methyl isobutyl ketone and xylene; flowing out agents such as nitrocellulose, ethyl cellulose, and ureaformaldehyde products; and catalysts e.g. 4-dimethylaminopyridine, iron and manganese acetylacetonates, antimony compounds, dibutyltin dilaurate, stannous octoate, lead acetate, basic lead acetate and lead 2-ethylhexoate. Examples are given of the production of polyurethane lacquers and foams.
GB3870961A 1961-10-30 1961-10-30 Manufacture of polyurethanes Expired GB971974A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3870961A GB971974A (en) 1961-10-30 1961-10-30 Manufacture of polyurethanes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3870961A GB971974A (en) 1961-10-30 1961-10-30 Manufacture of polyurethanes

Publications (1)

Publication Number Publication Date
GB971974A true GB971974A (en) 1964-10-07

Family

ID=10405208

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3870961A Expired GB971974A (en) 1961-10-30 1961-10-30 Manufacture of polyurethanes

Country Status (1)

Country Link
GB (1) GB971974A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3985699A (en) 1974-06-07 1976-10-12 Ab Bofors Method of manufacturing mould members of polyurethane-bonded granular material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3985699A (en) 1974-06-07 1976-10-12 Ab Bofors Method of manufacturing mould members of polyurethane-bonded granular material

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