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US4067820A
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US
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High molecular weight, insoluble carbodiimidization catalysts
Assignee: Bayer AG
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Filing: 1976-01-30
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Granted: 1978-01-10
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Expires: 1996-01-30
Abstract
Abstract The instant invention relates to novel carbodiimidization catalysts consisting of a high molecular weight, insoluble matrix and low molecular weight carbodiimidization catalysts fixed to the matrix via ionic bonds. The novel high molecular weight catalysts are suitable for the preparation of storage stable, catalyst free, equilibrium mixtures of organic carbodiimides, uretone imines and isocyanates. Either the carbodiimide, or the uretone imine or both may contain isocyanate groups. Alternatively, mono and/or polyisocyanates free from carbodiimide and uretone imine groups may be added to the equilibrium mixture. The catalysts according to the invention are capable of bringing about selective carbodiimidization of individual isocyanates in a mixture of various isocyanates.
Inventors
- 👤 Kuno Wagner
- 👤 Hans-Dieter Block
- 👤 Walter Schafer
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-02 03:57
CPC Classifications
B; B01; B01J; B01J31/00; B01J31/02; B01J31/0234; B01J31/0255; B01J31/0257; B01J31/0262; B01J31/0259; B01J31/06; B01J31/08; C; C08; C08G; C08G18/00; C08G18/06; C08G18/70; C08G18/72; C08G18/77; C08G18/78; C08G18/79; C08G18/797; B01J2231/00; B01J2231/30; B01J2231/34; B01J2231/341; Y; Y10; Y10S; Y10S521/00; Y10S521/901
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
39 words
High molecular weight carbodiimidization catalysts which are insoluble in water and in polyisocyanates and which consist of a high molecular weight, insoluble, organic or inorganic matrix and low molecular weight carbodiimidization catalysts bound to this matrix via ionic bonds.
Claim 2
Dependent Claim
39 words
High molecular weight carbodiimidization catalysts which are insoluble in water and in polyisocyanates and which consist of a high molecular weight, insoluble, organic or inorganic matrix and low molecular weight carbodiimidization catalysts bound to this matrix via ionic bonds.
Claim 3
Dependent Claim
29 words
Carbodiimidization catalysts according to claim 1 characterized in that the high molecular weight matrix contains basic ionizable groups and the low molecular weight carbodiimidization catalyst contains acid ionizable groups.
Claim 4
Dependent Claim
103 words
Carbodiimidization catalysts according to claim 2 characterized in that the low molecular weight carbodiimidization catalyst corresponds to the following general formula: ##STR59##wherein R 1 represents an alkyl, aryl or aralkyl group having up to 14 carbon atoms which may be substituted, preferably by halogen; R 2 , r 3 and R 4 each represent a C 1 -C 4 alkyl group, hydrogen, chlorine or bromine; R 5 represents hydrogen, a C 1 -C 12 alkyl group and, if b = 0 a C 6 -C 12 aryl group; X and Y represent oxygen or sulphur; and a and b = 0 or 1.
Claim 5
Dependent Claim
31 words
Carbodiimidization catalysts according to claim 3 characterized in that the high molecular weight matrix is a polystyrene which has been cross-linked with from 2 to 6% by weight of divinyl benzene.
Claim 6
Dependent Claim
52 words
A process for the preparation of high molecular weight carbodiimidization catalysts comprising contacting a high molecular weight, insoluble, inorganic or organic matrix which contains ionizable groups with a solution of low molecular weight carbodiimidization catalysts which contain ionizable groups, the charge of which is opposite in sign to that of the matrix.
Claim 7
Dependent Claim
52 words
A process for the preparation of high molecular weight carbodiimidization catalysts comprising contacting a high molecular weight, insoluble, inorganic or organic matrix which contains ionizable groups with a solution of low molecular weight carbodiimidization catalysts which contain ionizable groups, the charge of which is opposite in sign to that of the matrix.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1981-01-09 | 1981-07-11 | 1982-01-10 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1985-01-09 | 1985-07-11 | 1986-01-10 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1989-01-09 | 1989-07-11 | 1990-01-10 | $7700.00 | Window Closed / Lapsed |