GB1097504A - Elastomeric polyurethanes - Google Patents
Elastomeric polyurethanesInfo
- Publication number
- GB1097504A GB1097504A GB681266A GB681266A GB1097504A GB 1097504 A GB1097504 A GB 1097504A GB 681266 A GB681266 A GB 681266A GB 681266 A GB681266 A GB 681266A GB 1097504 A GB1097504 A GB 1097504A
- Authority
- GB
- United Kingdom
- Prior art keywords
- glycol
- glycols
- diol
- mixture
- polyester
- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
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
An elastomeric polyurethane is the reaction product of a diisocyanate, a polyester diol of molecular weight 700-2000, and a mixture of at least two different glycols, in proportions such that the overall ration of isocyanate to hydroxyl groups is about 1:1, while the polyester/glycol ratio ranges from 2:1 to 1:3. The glycol contains between the hydroxy groups a divalent aliphatic group containing 2-10 C atoms, of which 2-6 may form a chain separating the hydroxy groups, and optionally such groups as -O-, <FORM:1097504/C3/1> alkyl, -arylene-, and -O-arylene-O-. Examples are ethylene and tri-, tetra-, penta- and hexamethylene, neopentylene, diethylene, dipropylene, dibutylene glycols, ethyl and methyl diethanolamines, methyl dipropanolamine, p-xylylene diol, p-phenylene diethylene glycol and hydroquinone di-(ethylene glycol) ether. No glycol should comprise less than 20% of a mixture of two glycols, or less than 10% of a mixture of more than two glycols. Many conventional aromatic and aliphatic diisocyanates are listed. Suitable polyester diols may be derived from adipic, succinic, suberic, azelaic, sebacic and terephthalic acids or anhydrides with C2- 10 normal alkylene glycols, or from e -caprolactone polymerized with a glycol or aminoalkanol initiator. Suitable catalysts are metal compounds (lists), phosphines and tertiary amines, in amounts of 0.1-2 weight per cent of the reactants. The preparation preferably proceeds as a one-shot process, but it is possible to form a prepolymer from the diisocyanate and the polyester diol. Conventional pigments, fillers, and colouring agents may be added. In Examples 1, 2, 4 and 5, mixtures of two of trimethylene glycol, tetramethylene glycol and neopentylene glycol are mixed with a poly-(e-caprolactone) diol or a poly-(9:1-ethylenepropylene) adipate diol, then with diphenylmethane diisocyanate. In Example 7 toluenediisocyanate is used, and in Example 8 a mixture of tetramethylene and hexamethylene glycols.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US43842565A | 1965-03-09 | 1965-03-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1097504A true GB1097504A (en) | 1968-01-03 |
Family
ID=23740613
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB681266A Expired GB1097504A (en) | 1965-03-09 | 1966-02-16 | Elastomeric polyurethanes |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1645578A1 (en) |
GB (1) | GB1097504A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3103846A1 (en) | 2015-06-10 | 2016-12-14 | UBE Corporation Europe, S.A.U. | Self-healing polyurethane polymers |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2161340C3 (en) * | 1971-12-10 | 1982-02-18 | Bayer Ag, 5090 Leverkusen | Adhesive based on polyurethane |
DE2817456A1 (en) * | 1978-04-21 | 1979-10-31 | Bayer Ag | PROCESS FOR MANUFACTURING THERMOPLASTIC POLYURETHANE ELASTOMERS |
-
1966
- 1966-02-16 GB GB681266A patent/GB1097504A/en not_active Expired
- 1966-03-09 DE DE19661645578 patent/DE1645578A1/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3103846A1 (en) | 2015-06-10 | 2016-12-14 | UBE Corporation Europe, S.A.U. | Self-healing polyurethane polymers |
WO2016198441A1 (en) | 2015-06-10 | 2016-12-15 | Ube Corporation Europe, S.A.U. | Self-healing polyurethane polymers |
Also Published As
Publication number | Publication date |
---|---|
DE1645578A1 (en) | 1970-10-22 |
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