GB981135A - Improvements in the manufacture of cellular polyurethanes - Google Patents

Improvements in the manufacture of cellular polyurethanes

Info

Publication number
GB981135A
GB981135A GB4125862A GB4125862A GB981135A GB 981135 A GB981135 A GB 981135A GB 4125862 A GB4125862 A GB 4125862A GB 4125862 A GB4125862 A GB 4125862A GB 981135 A GB981135 A GB 981135A
Authority
GB
United Kingdom
Prior art keywords
diisocyanate
methyl
reaction mixture
oxide
per molecule
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
GB4125862A
Inventor
Arthur Ibbotson
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 GB4125862A priority Critical patent/GB981135A/en
Publication of GB981135A publication Critical patent/GB981135A/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
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6681Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
    • C08G18/6688Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3271

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Fireproofing Substances (AREA)

Abstract

Foamed polyurethanes may be prepared by reacting an organic polyisocyanate and a polyether containing at least two ether groups and two hydroxy groups per molecule, under such conditions that a foam forming gas is generated, and having in the reaction mixture an N-substituted dialkanolamine in an amount of at least 15% by weight of the polyether. The preferred polyethers are polymers and copolymers of ethylene oxide or propylene oxide, optionally prepared by polymerization in the presence of a substance having two or more active hydrogen atoms per molecule, such as ammonia and polydroxy compounds such as glycerol, triethanolamine and polyamines such as ethylene diamine and tolylene diamine. Other alkylene oxides may be used such as 1:2 butylene oxide and 2:3 butylene oxide. Many aliphatic and aromatic diisocyanates are listed as suitable polyisocyanates such as hexamethylene diisocyanate and tolylene 2:4-diisocyanate. Triisocyanate may also be used such as 2:4:6-triisocyanateotoluene. The foam forming gas may be generated by adding water to the reaction mixture to react with a proportion of the diisocyanate to produce carbon dioxide, or by incorporating a low boiling liquid having a boiling point not exceeding 75 DEG C. which will volatilize on heating. A combination of these two methods may be employed. Preferred low boiling liquids are halogenated alkanes containing fluorine, such as monofluorotrichloromethane, dibromodifluoromethane, 1:1:1 - trichloro - 2:2:2 - trifluoroethane, dichlorodifluoromethane, dichloromonofluoromethane, dichlorotetrafluoroethane, monochlorodifluoromethane, trifluoroethylbromide and mixtures thereof. Examples of suitable N-substituted dialkanolamines include N - methyl diethanolamine, N - ethyldiethanolamine, N-butyl diethanolamine, N-phenyldiethanolamine and N-methyl diisopropanolamine. Other additives which may be included are catalysts such as tertiary amines and soluble organic compounds of heavy metals such as iron and manganese acetyl acetonate, lead actoate, dibutyl tin dilaurate and stannous octoate, surface active agents, e.g. oxethylated phenols, oleyl alcohol, sulphated methyl oleate, polyalkyl or polaryl siloxanes and siloxane-oxyalkylene copolymers, flame retardants such as b -trichloroethylphosphate and dioctylphthalate, colouring matters and fillers such as carbon black and silica and colour stabilizers, whitening agents, and anti-oxidants such as tert-butylalcohol and sterically hindered phenols.
GB4125862A 1962-10-31 1962-10-31 Improvements in the manufacture of cellular polyurethanes Expired GB981135A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4125862A GB981135A (en) 1962-10-31 1962-10-31 Improvements in the manufacture of cellular polyurethanes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4125862A GB981135A (en) 1962-10-31 1962-10-31 Improvements in the manufacture of cellular polyurethanes

Publications (1)

Publication Number Publication Date
GB981135A true GB981135A (en) 1965-01-20

Family

ID=10418867

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4125862A Expired GB981135A (en) 1962-10-31 1962-10-31 Improvements in the manufacture of cellular polyurethanes

Country Status (1)

Country Link
GB (1) GB981135A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4256802A (en) * 1979-06-11 1981-03-17 The Upjohn Company Process for polyisocyanurate foams suitable for panels
EP0079115A1 (en) * 1981-10-28 1983-05-18 Imperial Chemical Industries Plc Polymer-modified polyols
WO1986001522A1 (en) * 1984-08-23 1986-03-13 The Dow Chemical Company An active hydrogen-containing composition containing a dialkanol tertiary amine and a process for preparing a polyurethane foam
JPS61501327A (en) * 1984-08-23 1986-07-03 ザ ダウ ケミカル カンパニ− Active hydrogen-containing composition containing dialkanol tertiary amine

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4256802A (en) * 1979-06-11 1981-03-17 The Upjohn Company Process for polyisocyanurate foams suitable for panels
EP0079115A1 (en) * 1981-10-28 1983-05-18 Imperial Chemical Industries Plc Polymer-modified polyols
WO1986001522A1 (en) * 1984-08-23 1986-03-13 The Dow Chemical Company An active hydrogen-containing composition containing a dialkanol tertiary amine and a process for preparing a polyurethane foam
JPS61501327A (en) * 1984-08-23 1986-07-03 ザ ダウ ケミカル カンパニ− Active hydrogen-containing composition containing dialkanol tertiary amine
US4632943A (en) * 1984-08-23 1986-12-30 Dow Chemical Company Polyurethane foams prepared from alkyl dialkanol amine-containing polyols
JPH0154364B2 (en) * 1984-08-23 1989-11-17 Dow Chemical Co

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