GB964266A - Improvements in and relating to polyurethane resins - Google Patents

Improvements in and relating to polyurethane resins

Info

Publication number
GB964266A
GB964266A GB4299261A GB4299261A GB964266A GB 964266 A GB964266 A GB 964266A GB 4299261 A GB4299261 A GB 4299261A GB 4299261 A GB4299261 A GB 4299261A GB 964266 A GB964266 A GB 964266A
Authority
GB
United Kingdom
Prior art keywords
propylene oxide
tris
oxide condensate
phosphate
polyols
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
GB4299261A
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.)
Union Carbide Corp
Original Assignee
Union Carbide 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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB964266A publication Critical patent/GB964266A/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
    • C08G18/48Polyethers

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 flame-resistant polyurethane foams comprises reacting a polyether having at least two hydroxyl groups and a molecular weight from 250 to 5000 and an organic polyisocyanate or polyisothiocyanate in the presence of a catalyst, a blowing agent and, as a flame-proofing additive, 0.5 to 10% by weight, based on the weight of the polyether and polyisocyanate or polyisothiocyanate, of tris (2,3-bibromopropyl)-phosphate. Antimony trioxide may be used in conjunction with the phosphate. Water and fluorocarbons are specified blowing agents. Suitable polyethers are reaction products of alkylene oxides with water, glycols, polyols, glycosides, sucrose, di, tri and tetraphenylol compounds, mono- and polynuclear and fused aromatic polyamines, novolaks and acyclic polyamines. Polyfunctional compounds such as aliphatic polyols can be blended with the polyethers before the reaction. Catalysts listed are stannous acylates, alkoxides, phenoxides and cresoxides; dialkyl tin carboxylates, chlorides or oxides and trialkyl tin hydroxides. A siloxaneoxyalkylene copolymer can be used as an emulsifying agent. In examples of the preparation of foams various amounts of the tris (2,3-dibromo propyl) phosphate together in some cases, with antimony trioxide are added to the reaction mixture. This comprises polyol mixture, prepolymer prepared from the polyol and excess tolylene diisocyanates, surfactant, dibutyl tin dilaurate, silicone and trichlorofluoromethane. Polyols used are (1) to (3), (5) and (6) a propylene oxide adduct of 1,1,3-tris-hydroxyphenyl, propane mixed with (1) hexanetriol, (2) and (5) glycerol/propylene oxide condensate, (3) di-ethylenetriamine/propylene oxide condensate, (6) 1,2,6-hexanetriol; (4) sorbitol/propylene oxide condensate; (7) methyl glucoside/propylene oxide condensate; (8) 4,41-diaminodiphenylmethane/propylene oxide. In (7) N,N,N1,N1-tetramethyl-1,3-butane diamine is also present as a catalyst. Specifications 666,732, 701,794 and 804,369 are referred to.
GB4299261A 1960-12-30 1961-12-01 Improvements in and relating to polyurethane resins Expired GB964266A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US7949060A 1960-12-30 1960-12-30

Publications (1)

Publication Number Publication Date
GB964266A true GB964266A (en) 1964-07-22

Family

ID=22150888

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4299261A Expired GB964266A (en) 1960-12-30 1961-12-01 Improvements in and relating to polyurethane resins

Country Status (3)

Country Link
DE (1) DE1156227B (en)
GB (1) GB964266A (en)
NL (1) NL273076A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3461086A (en) * 1964-03-05 1969-08-12 Dow Chemical Co Polyether urethane foams from certain heteric polyethers
DE1229289B (en) * 1965-01-22 1966-11-24 Bayer Ag Process for the manufacture of plastics containing urethane groups, including foams

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1043630B (en) * 1955-12-24 1958-11-13 Phoenix Gummiwerke Ag Process for the production of rigid, flame-retardant foam plastics

Also Published As

Publication number Publication date
NL273076A (en)
DE1156227B (en) 1963-10-24

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