Radiation curable polyurethane-based binder dispersion
US-2018179325-A1 · Jun 28, 2018 · US
US10920094B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10920094-B2 |
| Application number | US-201716335460-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 31, 2017 |
| Priority date | Jan 31, 2017 |
| Publication date | Feb 16, 2021 |
| Grant date | Feb 16, 2021 |
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The present disclosure is drawn to a reactive polyurethane dispersion including a polymer strand having a polymer backbone that has two ends terminating at a first capping unit and a second capping unit. The polymer backbone can include polymerized monomers including a reactive diol and a diisocyanate. The reactive diol can be an acrylate-containing diol, a methacrylate-containing diol, a styrene-containing diol, or combination thereof. The first capping unit can be a styrene-containing monoalcohol reacted with an isocyanate group of the diisocyanate. The second capping unit can be an ionic stabilizing group.
Opening claim text (preview).
What is claimed is: 1. A reactive polyurethane dispersion, comprising a polymer strand comprising a polymer backbone having two terminating ends comprising a first capping unit at a first terminating end and a second capping unit at a second terminating end, wherein the polymer backbone comprises polymerized monomers including: a reactive diol selected from an acrylate-containing diol, a methacrylate-containing diol, a styrene-containing diol, or combination thereof, and a diisocyanate; wherein the first capping unit is a styrene-containing monoalcohol reacted with an isocyanate group of the diisocyanate; and wherein the second capping unit is an ionic stabilizing group. 2. The reactive polyurethane dispersion of claim 1 , wherein the polymer backbone is devoid of ionic stabilizing groups. 3. The reactive polyurethane dispersion of claim 1 , wherein the reactive polyurethane dispersion has a NCO/OH ratio of 1.2 to 10. 4. The reactive polyurethane dispersion of claim 1 , wherein the reactive polyurethane dispersion has an acid number of 20 to 100. 5. The reactive polyurethane dispersion of claim 1 , wherein the reactive polyurethane dispersion has a double bond density of 1.5 to 10. 6. The reactive polyurethane dispersion of claim 1 , wherein the reactive diol is selected from: or a combination thereof. 7. The reactive polyurethane dispersion of claim 1 , wherein the styrene-containing monoalcohol is selected from: or a combination thereof. 8. The reactive polyurethane dispersion of claim 1 , wherein the reactive polyurethane dispersion is devoid of polymer strands having capping units that include acrylate groups or methacrylate groups. 9. The reactive polyurethane dispersion of claim 1 , wherein a majority of polymer strands in the reactive polyurethane dispersion have a first capping unit that is a styrene-containing monoalcohol reacted with an isocyanate group of the diisocyanate and a second capping unit that is an ionic stabilizing group. 10. A UV-curable ink composition, comprising: a colorant; a photoinitiator; and a reactive polyurethane dispersion, comprising a polymer strand comprising a polymer backbone having two terminating ends comprising a first capping unit at a first terminating end and a second capping unit at a second terminating end, wherein the polymer backbone comprises polymerized monomers including: a reactive diol selected from an acrylate-containing diol, a methacrylate-containing diol, a styrene-containing diol, or combination thereof, and a diisocyanate; wherein the first capping unit is a styrene-containing monoalcohol reacted with an isocyanate group of the diisocyanate; and wherein the second capping unit is an ionic stabilizing group. 11. The UV-curable ink composition of claim 10 , wherein the UV-curable ink composition has a pH of 7.0 to 11.5. 12. The UV-curable ink composition of claim 11 , wherein the pH does not decrease by more than 1.0 when the UV-curable ink composition is exposed to accelerated shelf life (ASL) at 50° C. in open air for 1 week. 13. The UV-curable ink composition of claim 10 , wherein the polymer backbone is devoid of ionic stabilizing groups. 14. A method of making a reactive polyurethane dispersion, comprising: reacting a diisocyanate with a reactive diol selected from an acrylate-containing diol, a methacrylate-containing diol, a styrene-containing diol, or combination thereof, to form a first pre-polymer; reacting the first pre-polymer with a styrene-containing monoalcohol to form a second pre-polymer; reacting the second pre-polymer with an acid-containing amine to form a polymer strand; and dispersing the polymer strand in water to form the reactive polyurethane dispersion. 15. The method of claim 14 , further comprising adding a colorant and a photoinitiator to the reactive polyurethane dispersion to form a UV-curable ink composition. 16. The method of claim 15 , further comprising adding a cross-linker to the U V-curable ink composition. 17. The method of claim 14 , wherein the styrene-containing monoalcohol is selected from: or a combination thereof. 18. The UV-curable ink composition of claim 10 , further comprising a cross-linker. 19. The UV-curable ink composition of claim 10 , wherein the reactive diol is selected from: or a combination thereof. 20. The UV-curable ink composition of claim 10 , wherein the styrene-containing monoalcohol is selected from: or a combination thereof.
having nitrogen in addition to sulfur · CPC title
with nitrogen containing compounds · CPC title
having terminal carbon-to-carbon unsaturated bonds · CPC title
Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing · CPC title
with unsaturated monofunctional alcohols or amines · CPC title
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