GB885234A - Polyurethane compositions - Google Patents
Polyurethane compositionsInfo
- Publication number
- GB885234A GB885234A GB2057757A GB2057757A GB885234A GB 885234 A GB885234 A GB 885234A GB 2057757 A GB2057757 A GB 2057757A GB 2057757 A GB2057757 A GB 2057757A GB 885234 A GB885234 A GB 885234A
- Authority
- GB
- United Kingdom
- Prior art keywords
- catalyst
- polyisocyanate
- piperazine
- reactants
- hydrogen
- 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
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
- C08G18/20—Heterocyclic amines; Salts thereof
- C08G18/2009—Heterocyclic amines; Salts thereof containing one heterocyclic ring
- C08G18/2027—Heterocyclic amines; Salts thereof containing one heterocyclic ring having two nitrogen atoms in the ring
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
Odourless polyurethane compositions comprise the reaction product of a polyisocyanate, an active hydrogen-containing compound, and an amount, preferably 0,25 to 5,0 parts per 100 parts of the other two reactants, of an N,N1-bis (2-hydroxyalkyl) piperazine as catalyst. By including water among the reactants foamed products are obtained. The catalyst conforms to the structural formula <FORM:0885234/IV (a)/1> wherein R1 and R2, and R3, R4, R5 and R6 are hydrogen, alkyl, aryl or alkylaryl; R1 and R2 are preferably ethyl or propyl groups, and 2-methyl-and 2,5-dimethyl piperazine compounds are preferred. Specified reactive hydrogen-containing compounds include polyesters, polyesteramides, polyalcohols, and polyether alcohols. Suitable polyisocyanates are listed in the Specification and include ethylene-, propylene 1,2-, butylene 1,3-, cyclohexylane 1,2- 2,4- toluene-, triphenylmethane-, 3,31-dimethyl-, and 4,4-biphenylenediisocyanate. The polyurethane reaction may be effected by conventional technique, e.g. all the reactants may be simultaneously mixed together or the catalyst may be dissolved in water and the reactive hydrogen-containing organic compound added, followed by polyisocyanate; alternatively excess polyisocyanate may be reacted with reactive hydrogen-containing compound and aqueous piperazine catalyst solution added to the "prepolymer" formed in amount stoichiometrically equivalent to the "free" isocyanate content thereof. Reference has been directed by the Comptroller to Specifications 754,502 and 795,276.ALSO:Odourless foamed polyurethane products comprise the reaction product of water, a polyisocyanate, an active hydrogen-containing compound, and an amount, preferably 0,25 to 5,0 parts per 100 parts of the former two reactants, of an N-N1 bis (2-hydroxyalkyl) piperazine as catalyst which conforms to the structural formula:- <FORM:0885234/V/1> wherein R1 and R2, and R3, R4, R5 and R6 are hydrogen, alkyl, aryl, or alkylaryl; R1 and R2 are preferably ethyl or propyl groups; 2-methyl-and 25-dimethyl substituted piperazine compounds are preferred. Specified reactive hydrogen-containing compounds include polyesters, polyesteramides, polyalcohols, and polyether alcohols. Suitable polyisocyanates are listed in the Specification and include ethylenepropylene 1,2-; butylene 1,3-; cyclohexene 1,2-; 2,4-toluene-; triphenylmethane-, 3,31-dimethyl-; and 4,4 biphenylene-, diisocyanates. The polyurethane reaction may be effected by conventional techniques, e.g. all the reactants may be simultaneously mixed together or the catalyst may be dissolved in water and the reactive hydrogen-containing organic compound added, followed by polyisocyanate; alternatively excess polyisocyanate may be reacted with reactive hydrogen-containing compound and aqueous piperazine catalyst solution added to the "prepolymer" formed, in amount stocchiometrically equivalent to the "free" isocyanate content thereof. Reference has been directed by the Comptroller to Specifications 754,502 and 795,276.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2057757A GB885234A (en) | 1957-06-28 | 1957-06-28 | Polyurethane compositions |
| DEW23489A DE1089164B (en) | 1957-06-28 | 1958-06-12 | Process for the production of odorless, crosslinked, optionally foam-shaped polyurethanes |
| FR1208564D FR1208564A (en) | 1957-06-28 | 1958-06-21 | Improvements to polyurethane-based compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2057757A GB885234A (en) | 1957-06-28 | 1957-06-28 | Polyurethane compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB885234A true GB885234A (en) | 1961-12-20 |
Family
ID=10148208
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2057757A Expired GB885234A (en) | 1957-06-28 | 1957-06-28 | Polyurethane compositions |
Country Status (3)
| Country | Link |
|---|---|
| DE (1) | DE1089164B (en) |
| FR (1) | FR1208564A (en) |
| GB (1) | GB885234A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2231878A (en) * | 1989-05-22 | 1990-11-28 | Basf Corp | Molded flexible polyurethane compositions of polycarbonate compatibility |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4500654A (en) * | 1983-11-01 | 1985-02-19 | Abbott Laboratories | Catalyst system and process for the production of polyurethanes |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE926880C (en) * | 1952-01-30 | 1955-04-25 | Bayer Ag | Process for the production of foams with a very low specific weight |
| DE954376C (en) * | 1953-05-23 | 1956-12-13 | Bayer Ag | Process for the production of crosslinked plastics |
-
1957
- 1957-06-28 GB GB2057757A patent/GB885234A/en not_active Expired
-
1958
- 1958-06-12 DE DEW23489A patent/DE1089164B/en active Pending
- 1958-06-21 FR FR1208564D patent/FR1208564A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2231878A (en) * | 1989-05-22 | 1990-11-28 | Basf Corp | Molded flexible polyurethane compositions of polycarbonate compatibility |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1089164B (en) | 1960-09-15 |
| FR1208564A (en) | 1960-02-24 |
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