GB1189997A - Polyether-Urethanes - Google Patents
Polyether-UrethanesInfo
- Publication number
- GB1189997A GB1189997A GB4323366A GB4323366A GB1189997A GB 1189997 A GB1189997 A GB 1189997A GB 4323366 A GB4323366 A GB 4323366A GB 4323366 A GB4323366 A GB 4323366A GB 1189997 A GB1189997 A GB 1189997A
- Authority
- GB
- United Kingdom
- Prior art keywords
- triol
- glycol
- reaction
- liquid
- prepolymers
- 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
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6674—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
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
1,189,997. Polyetherurethanes. PFIZER Ltd. 27 Sept., 1967 [28 Sept., 1966], No. 43233/66. Headings C3C and C3R. Liquid polyetherurethane prepolymers having a free isocyanate content are prepared by reacting, in the absence of a catalyst: (A) an aromatic diisocyanate; (B) a linear, liquid alpha-omega glycol having an hydroxyl equivalent weight below 250; and (C) a liquid polyoxyalkylene triol having an hydroxyl equivalent weight of at least 250, the ratio of isocyanate groups in (A) to hydroxyl groups in (B) plus (C) being greater than one and the proportion of triol (C) to glycol (B) being such that the reaction product is a stable liquid, i.e. a liquid which does not crystallize within 24 hours at ambient temperatures. The compounds (A), (B) and (C) are those conventionally used in the art. Especially preferred as glycol (B) is diethylene glycol which may be used such that the weight ratio of triol (C) to diethylene glycol is at least 4 to 1, preferably 6 to 1. The reaction between (A), (B) and (C) is preferably carried out at temperatures of 55‹ to 90‹ C. Elastomers may be prepared from the prepolymers by reaction with further amounts of glycol (B) and/or triol (C) in the presence of an organometallic catalyst such that the ratio of isocyanate groups to hydroxyl groups is in the range of 0À95 to 1 to 1À2 to 1. Alternatively the prepolymer may be reacted with other compounds containing two or more hydroxyl and/or primary amine groups or may be dissolved in a solvent with a tertiary amine catalyst and allowed to cure by reaction with moisture in the atmosphere. Microcellular elastomers may be prepared from the prepolymers by reaction with further amounts of (B) and/or (C) in the presence of small amounts of air and/or water and, if desired, a nucleating agent. The additional triol (C) may be partially or entirely replaced by an inert plasticizer such as phthalic acid esters and chlorinated hydrocarbons. Numerous examples are given of the polyetherurethane prepolymers and elastomers prepared therefrom.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4323366A GB1189997A (en) | 1966-09-28 | 1966-09-28 | Polyether-Urethanes |
DE19671745276 DE1745276A1 (en) | 1966-09-28 | 1967-09-23 | Polyaether urethanes and processes for their preparation |
FR122335A FR1538174A (en) | 1966-09-28 | 1967-09-26 | Improvements in processes for the preparation and use of polyetherurethanes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4323366A GB1189997A (en) | 1966-09-28 | 1966-09-28 | Polyether-Urethanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1189997A true GB1189997A (en) | 1970-04-29 |
Family
ID=10427849
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4323366A Expired GB1189997A (en) | 1966-09-28 | 1966-09-28 | Polyether-Urethanes |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1745276A1 (en) |
GB (1) | GB1189997A (en) |
-
1966
- 1966-09-28 GB GB4323366A patent/GB1189997A/en not_active Expired
-
1967
- 1967-09-23 DE DE19671745276 patent/DE1745276A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
DE1745276A1 (en) | 1971-08-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |