GB858757A - Synthetic rubber-like materials - Google Patents
Synthetic rubber-like materialsInfo
- Publication number
- GB858757A GB858757A GB2820357A GB2820357A GB858757A GB 858757 A GB858757 A GB 858757A GB 2820357 A GB2820357 A GB 2820357A GB 2820357 A GB2820357 A GB 2820357A GB 858757 A GB858757 A GB 858757A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyesteramide
- reacting
- diisocyanate
- acid
- raw rubber
- 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
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/60—Polyamides or polyester-amides
- C08G18/606—Polyester-amides
Abstract
A process for the manufacture of synthetic rubber-like materials by reacting organic diisocyantes with polyesteramides, is characterized in that the said reaction is carried out under substantially anhydrous conditions and that the polyesteramide is based on dicarboxylic acid, glycol and diamine and/or aminoalcohol in such proportions that from 8 to 64 mols. of dicarboxylic acid are present for each mol. of primary amino group and the polyesteramide is crystalline with a melting point not exceeding 50 DEG C and has a water content of not more than 0,1% by weight and an acid value of not more than 5 mg. KOH per gm. and preferably not more than 3 mg. KOH per gm. The process may be effected in one step by mixing the polyesteramide and all the diisocyanate, casting and heating in a mould. Preferably a "raw rubber" is produced in a first stage by reacting such an amount of diisocyanate as to give a processible reaction product with a Williams Plasticity Number between 200 and 550. The "raw rubber" is then processed with an organic polyisocyanate and there may also be incorporated fillers such as carbon black, silica, china clay, calcium carbonate, titanium dioxide, aluminium silicate and fibres such as those of glass, polyesters, polyamides, wool and ground leather, plasticizers, catalysts, acids such as adipic and stearic and materials capable of forming adducts with isocyanates. Curing is then effected with heating and pressure. In a typical Example (12) a "raw rubber" of Williams Plasticity Number 289 is prepared by reacting mixed toluene -2,4 and 2,6- diisocyanates with a polyesteramide prepared by reacting adipic acid, ethylene glycol, diethylene glycol and ethanolamine. It is milled with stearic acid, silica and 4:41 diisocyanate -3- methyldiphenylmethane and press cured at 150 DEG C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2820357A GB858757A (en) | 1957-09-06 | 1957-09-06 | Synthetic rubber-like materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2820357A GB858757A (en) | 1957-09-06 | 1957-09-06 | Synthetic rubber-like materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB858757A true GB858757A (en) | 1961-01-18 |
Family
ID=10271940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2820357A Expired GB858757A (en) | 1957-09-06 | 1957-09-06 | Synthetic rubber-like materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB858757A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3345338A (en) * | 1962-08-11 | 1967-10-03 | Bayer Ag | Polyurethanes prepared from amino polyesters |
EP0235887A1 (en) * | 1986-02-05 | 1987-09-09 | Imperial Chemical Industries Plc | The use of polyester polyols for preparing microcellular polyurethane elastomers |
WO1997021759A2 (en) * | 1995-12-14 | 1997-06-19 | Bk Giulini Chemie Gmbh | New hydrolysis-resistant aliphatic polyester amides, their production and use |
-
1957
- 1957-09-06 GB GB2820357A patent/GB858757A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3345338A (en) * | 1962-08-11 | 1967-10-03 | Bayer Ag | Polyurethanes prepared from amino polyesters |
EP0235887A1 (en) * | 1986-02-05 | 1987-09-09 | Imperial Chemical Industries Plc | The use of polyester polyols for preparing microcellular polyurethane elastomers |
US4801736A (en) * | 1986-02-05 | 1989-01-31 | Imperial Chemical Industries Plc | Polyester polyols containing monoalkanolamine derived units |
JP2549645B2 (en) | 1986-02-05 | 1996-10-30 | インペリアル・ケミカル・インダストリ−ズ・ピ−エルシ− | Method for producing microcellular polyurethane |
WO1997021759A2 (en) * | 1995-12-14 | 1997-06-19 | Bk Giulini Chemie Gmbh | New hydrolysis-resistant aliphatic polyester amides, their production and use |
WO1997021759A3 (en) * | 1995-12-14 | 1997-09-12 | Giulini Chemie | New hydrolysis-resistant aliphatic polyester amides, their production and use |
US6268465B1 (en) | 1995-12-14 | 2001-07-31 | Bk Giulini Chemie Gmbh Co Ohg | Hydrolysis-resistant aliphatic polyester amides, their production and use |
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