Process for the preparation of aqueous dispersions containing both blocked polyisocyanates and polyhydroxyl compounds
First Claim
1. A process for the preparation of an aqueous dispersion containing both a blocked polyisocyanate and a polyhydroxyl compound which comprises reacting an aqueously dispersed polyisocyanate having an isocyanate content of at least 12% by weight, based on the weight of the polyisocyanate, with a monofunctional blocking agent which is more reactive with isocyanate groups than water at an equivalent ratio of monofunctional blocking groups to isocyanate groups of 0.5:
- 1 to 2;
1 in the presence of a polyhydroxyl compound which is either water soluble or water dispersible, wherein the polyhydroxyl compound is present in an amount which is sufficient to provide an equivalent ratio of hydroxyl groups to blocked isocyanate groups of 0.6;
1 to 1.25;
1.
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Abstract
The present invention is directed to a process for the preparation of an aqueous dispersion containing both a blocked polyisocyanate and a polyhydroxyl compound by reacting an aqueously dispersed polyisocyanate having an isocyanate content of at least 12% by weight, based on the weight of the polyisocyanate, with a monofunctional blocking agent which is more reactive with isocyanate groups than water at an equivalent ratio of monofunctional blocking groups to isocyanate groups of 0.5:1 to 2:1 in the presence of a polyhydroxyl compound which is either water soluble or water dispersible, wherein the polyhydroxyl compound is present in an amount which is sufficient to provide an equivalent ratio of hydroxyl groups to blocked isocyanate groups of 0.6:1 to 1.25:1.
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Citations
12 Claims
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1. A process for the preparation of an aqueous dispersion containing both a blocked polyisocyanate and a polyhydroxyl compound which comprises reacting an aqueously dispersed polyisocyanate having an isocyanate content of at least 12% by weight, based on the weight of the polyisocyanate, with a monofunctional blocking agent which is more reactive with isocyanate groups than water at an equivalent ratio of monofunctional blocking groups to isocyanate groups of 0.5:
- 1 to 2;
1 in the presence of a polyhydroxyl compound which is either water soluble or water dispersible, wherein the polyhydroxyl compound is present in an amount which is sufficient to provide an equivalent ratio of hydroxyl groups to blocked isocyanate groups of 0.6;
1 to 1.25;
1. - View Dependent Claims (2, 3, 4, 5, 6)
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3. The process of claim 1 wherein said dispersed polyisocyanate is rendered hydrophilic by reaction with a compound containing a lateral or terminal nonionic hydrophilic group.
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4. The process of claim 1 wherein said equivalent ratio of monofunctional blocking groups to isocyanate groups is 0.8:
- 1.0 to 1.2;
1.0.
- 1.0 to 1.2;
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5. The process of claim 2 wherein said equivalent ratio of monofunctional blocking groups to isocyanate groups is 0.8:
- 1.0 to 1.2;
1.0.
- 1.0 to 1.2;
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6. The process of claim 3 wherein said equivalent ratio of monofunctional blocking groups to isocyanate groups is 0.8:
- 1.0 to 1.2;
1.0.
- 1.0 to 1.2;
- 1 to 2;
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7. A process for the preparation of an aqueous dispersion containing both a blocked polyisocyanate and a polyhydroxyl compound which comprises reacting an aqueously dispersed polyisocyanate having an isocyanate content of at least 12% by weight, based on the weight of the polyisocyanate, with a monofunctional blocking agent which is more reactive with isocyanate groups than water at an equivalent ratio of monofunctional blocking groups to isocyanate groups of 0.5:
- 1 to 2;
1 in the presence of a polyhydroxyl compound which is water soluble and has a molecular weight of 62 to less than 400, wherein the polyhydroxyl compound is present in an amount which is sufficient to provide an equivalent ratio of hydroxyl groups to blocked isocyanate groups of 0.6;
1 to 1.25;
1. - View Dependent Claims (8, 9, 10, 11, 12)
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9. The process of claim 7 wherein said dispersed polyisocyanate is rendered hydrophilic by reaction with a compound containing a lateral or terminal nonionic hydrophilic group.
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10. The process of claim 7 wherein said equivalent ratio of monofunctional blocking groups to isocyanate groups is 0.8:
- 1.0 to 1.2;
1.0.
- 1.0 to 1.2;
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11. The process of claim 8 wherein said equivalent ratio of monofunctional blocking groups to isocyanate groups is 0.8:
- 1.0 to 1.2;
1.0.
- 1.0 to 1.2;
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12. The process of claim 9 wherein said equivalent ratio of monofunctional blocking groups to isocyanate groups is 0.8:
- 1.0 to 1.2;
1.0.
- 1.0 to 1.2;
- 1 to 2;
Specification