GB887288A - Improvements in or relating to the manufacture of polyurethanes - Google Patents

Improvements in or relating to the manufacture of polyurethanes

Info

Publication number
GB887288A
GB887288A GB2566459A GB2566459A GB887288A GB 887288 A GB887288 A GB 887288A GB 2566459 A GB2566459 A GB 2566459A GB 2566459 A GB2566459 A GB 2566459A GB 887288 A GB887288 A GB 887288A
Authority
GB
United Kingdom
Prior art keywords
glycerol
hexanetriols
triethanolamine
acid
glycol
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
GB2566459A
Inventor
Herbert Gudgeon
Gord On Trappe
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 GB2566459A priority Critical patent/GB887288A/en
Publication of GB887288A publication Critical patent/GB887288A/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
    • C08G18/24Catalysts containing metal compounds of tin
    • C08G18/244Catalysts containing metal compounds of tin tin salts of carboxylic acids
    • C08G18/246Catalysts containing metal compounds of tin tin salts of carboxylic acids containing also tin-carbon bonds

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 elastomeric materials by reacting hydroxyl group-containing polymers containing at least two hydroxyl groups per molecule, such as polyesters, polyesteramides and polyethers, with organic polyisocyanates, is characterized in that the reaction is carried out in the presence of a tin compound of the formula R1R11SnX1X11 wherein R1 and R11 are alkyl groups which may be the same or different and X1 and X11 are organic acid radicals which may be the same or different. Specified tin compounds are those containing such alkyl groups as n-propyl, n-butyl, n-octyl or cyclohexyl and as acid radicals acetate, laurate, naphthenate, phenate, 2-ethyl hexoate or maleate. They are usually employed in about 0,01 to 5% by weight based on the weight of the polymer. The polymer usually has a hydroxyl value between 20 and 250. Glycols, dicarboxylic acids, hydroxy acids and amino compounds from which the polymers can be prepared are listed. Branching components such as glycerol, hexanetriols, triethanolamine, pentarythritol, trimesic acid, polymethacrylic acid, diethanolamine and dihydroxystearic acid are among the reactants specified. The polyethers can be those prepared from cyclic oxides in the presence of initiators such as water, diethylene glycol, hexanetriols, glycerol, triethanolamine, ethylene diamine, ethanolamine, sucrose or sorbitol. Particularly preferred are polymers containing predominantly secondary hydroxyl end-groups, such as polyesters and polyesteramides prepared from components including 1;2-propylene glycol, 1;3-butylene glycol, 2;3-butylene glycol and glycerol, and especially polymers obtained by polymerizing propylene oxide in the presence of, for example, hexanetriols, triethanolamine, glycerol, hexamethylene diamine, sorbitol, castor oil and castor oil derivatives. Preferred reactants for the polyurethane include at least one compound with more than 2 isocycanate or isocyanate-reactive groups per molecule. Pigments, fillers, plasticizers, antioxidants, stabilizers such as tert.-butyl catechol. In Examples (1) a linear polypropylene glycol and tolylene -2:4- and 2:6-diisocyanates are heated in the presence of dibutyl tin dilaurate. After cooling a glycerol/propylene oxide product is added and the mixture poured into a mould and cured by heating; (2) a hexanetriol/propylene oxide product is added to the initial reaction product in a similar process to (1). Uses. Printers rollers, potting and encapuslating compositions, and shock absorbers.
GB2566459A 1959-07-27 1959-07-27 Improvements in or relating to the manufacture of polyurethanes Expired GB887288A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2566459A GB887288A (en) 1959-07-27 1959-07-27 Improvements in or relating to the manufacture of polyurethanes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2566459A GB887288A (en) 1959-07-27 1959-07-27 Improvements in or relating to the manufacture of polyurethanes

Publications (1)

Publication Number Publication Date
GB887288A true GB887288A (en) 1962-01-17

Family

ID=10231314

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2566459A Expired GB887288A (en) 1959-07-27 1959-07-27 Improvements in or relating to the manufacture of polyurethanes

Country Status (1)

Country Link
GB (1) GB887288A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102295761A (en) * 2011-07-11 2011-12-28 华润包装材料有限公司 Method for preparing polyester for foaming

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102295761A (en) * 2011-07-11 2011-12-28 华润包装材料有限公司 Method for preparing polyester for foaming

Similar Documents

Publication Publication Date Title
US3489723A (en) Two-component castable polyurethane elastomer composition and use
US3164557A (en) Polyurethane production catalyzed by an organo-tin compound, which compound containstertiary nitrogen
US3016365A (en) Polythioetherurethane casting and method of preparing same
GB783564A (en) Process for the production of cross-linked diisocyanate-modified polyesters of high molecular weight
GB933683A (en)
JPS58188643A (en) Manufacture of reaction injection molding elastomer
US2958704A (en) Alkenyl isocyanate-substituted carbamates
GB967441A (en) Improvements in or relating to polyurethanes
US3051687A (en) Polyurethane resins
JPH0314845B2 (en)
FR2488897A1 (en) PROCESS FOR THE PREPARATION OF A POLYURETHANE ELASTOMER BY REACTION INJECTION MOLDING AND THE FORMED ARTICLE OBTAINED THEREBY
KR930007874B1 (en) Elastomers prepared from n-(polyoxyalkyl)-n-(alkyl) amines
US3523103A (en) Process for polyurethane formation and catalysts therefor
US3012991A (en) Chemical reactions
US3661885A (en) Polyurethane catalyst
CA3056061A1 (en) Oligomeric polyol compositions
GB912555A (en) Ordered isocyanate-terminated polyether-based urethanes
GB983586A (en) Polyurethanes and their manufacture
JPH0136845B2 (en)
GB984474A (en) Phosphorus containing polyurethanes
US3134755A (en) Polyurethane plastics prepared from the reaction product of an aldehyde and an oxyalkylated aromatic amine
GB796043A (en) Improvements in or relating to the preparation of polyurethane elastomers
GB887288A (en) Improvements in or relating to the manufacture of polyurethanes
US4120834A (en) Modified polyols
ES254953A1 (en) Method of making polyurethane thread and thread produced by such method