GB887288A - Improvements in or relating to the manufacture of polyurethanes - Google Patents
Improvements in or relating to the manufacture of polyurethanesInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/24—Catalysts containing metal compounds of tin
- C08G18/244—Catalysts containing metal compounds of tin tin salts of carboxylic acids
- C08G18/246—Catalysts 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.
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)
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 |
-
1959
- 1959-07-27 GB GB2566459A patent/GB887288A/en not_active Expired
Cited By (1)
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 |
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