GB1049288A - Polyurethanes - Google Patents

Polyurethanes

Info

Publication number
GB1049288A
GB1049288A GB2720262A GB2720262A GB1049288A GB 1049288 A GB1049288 A GB 1049288A GB 2720262 A GB2720262 A GB 2720262A GB 2720262 A GB2720262 A GB 2720262A GB 1049288 A GB1049288 A GB 1049288A
Authority
GB
United Kingdom
Prior art keywords
polyether
hydroxyl ended
hydroxyl
hydroxyethylamino
triazine
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
GB2720262A
Inventor
John Langrish
Raymond Joseph Marklow
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 GB2720262A priority Critical patent/GB1049288A/en
Publication of GB1049288A publication Critical patent/GB1049288A/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
    • C08G18/50Polyethers having heteroatoms other than oxygen
    • C08G18/5021Polyethers having heteroatoms other than oxygen having nitrogen
    • C08G18/5054Polyethers having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring
    • C08G18/5063Polyethers having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring containing three nitrogen atoms in the ring

Abstract

A polyether of OH No. 343 is prepared by reacting tris (di-b -hydroxyethylamino) 1:3:5 triazine with propylene oxide, the latter being added in two stages.ALSO:Polyurethanes are prepared by reacting an organic polyisocyanate and a hydroxyl ended polyether of formula <FORM:1049288/C3/1> wherein R, R1, R11, R111, RIV and RV each stand for a hydrogen atom, an alkyl group or a hydroxyl ended polyether chain, at least two of the groups R being hydroxyl ended polyether chains. The hydroxyl ended polyether may have a M.W. of 300-10,000 and may be the oxyalkylation product of a hydroxy alkyl derivative of melamine. In the preparation of foams, surface coatings and adhesives the hydroxy ended polyether preferably contains at least three isocyanate reactive groupings. In an example a polyether of OH No. 343 was prepared from tris(di-b -hydroxyethylamino)-1:3:5-triazine and propylene oxide, the latter being added in two stages. The polyether was mixed with water, butylated urea formaldehyde, cyclohexanone, methyl isobutyl ketone and a solution of a phosgenated crude diaminodiphenylmethane to obtain a coating solution.ALSO:Substrates e.g. wood, rubber, metals, glass and fabrics are coated with a polyurethane coating composition obtained by reacting an organic polyisocyanate with a polyether of formula <FORM:1049288/B1-B2/1> where the groups R each stand for hydrogen, alkyl or a hydroxyl ended polyether chain, at least two of the groups R being hydroxyl ended polyether chains. In an example a polyurethane obtained from propoxylated tris (di-b hydroxyethylamino) - 1 : 3 : 5 triazine by reaction with a phosgenated crude diamino diphenylmethane in admixture with water, xylene, cyclhexanone, methyl isobutyl ketone, and butylated urea formaldehyde was applied by spinning to steel panels or by dipping to steel rods and dried.
GB2720262A 1962-07-16 1962-07-16 Polyurethanes Expired GB1049288A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2720262A GB1049288A (en) 1962-07-16 1962-07-16 Polyurethanes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2720262A GB1049288A (en) 1962-07-16 1962-07-16 Polyurethanes

Publications (1)

Publication Number Publication Date
GB1049288A true GB1049288A (en) 1966-11-23

Family

ID=10255840

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2720262A Expired GB1049288A (en) 1962-07-16 1962-07-16 Polyurethanes

Country Status (1)

Country Link
GB (1) GB1049288A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1279686A2 (en) * 2001-07-26 2003-01-29 Agrolinz Melamin GmbH Polymers from triazine derivatives
EP2128144A1 (en) * 2008-05-30 2009-12-02 Basf Se Amphiphilic molecules with a triazine core
WO2009144274A2 (en) * 2008-05-30 2009-12-03 Basf Se Amphiphilic molecules with a triazine core
CN107602789A (en) * 2017-09-29 2018-01-19 鹤山市杰之星五金实业有限公司 A kind of plant polyatomic alcohol and its soft polyurethane foam containing plant polyatomic alcohol
CN112552979A (en) * 2020-11-27 2021-03-26 广东石油化工学院 Antiwear agent and preparation method thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1279686A2 (en) * 2001-07-26 2003-01-29 Agrolinz Melamin GmbH Polymers from triazine derivatives
EP1279686A3 (en) * 2001-07-26 2004-01-14 Agrolinz Melamin GmbH Polymers from triazine derivatives
EP2128144A1 (en) * 2008-05-30 2009-12-02 Basf Se Amphiphilic molecules with a triazine core
WO2009144274A2 (en) * 2008-05-30 2009-12-03 Basf Se Amphiphilic molecules with a triazine core
WO2009144274A3 (en) * 2008-05-30 2010-05-14 Basf Se Amphiphilic molecules with a triazine core
CN107602789A (en) * 2017-09-29 2018-01-19 鹤山市杰之星五金实业有限公司 A kind of plant polyatomic alcohol and its soft polyurethane foam containing plant polyatomic alcohol
CN112552979A (en) * 2020-11-27 2021-03-26 广东石油化工学院 Antiwear agent and preparation method thereof

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