Method for applying nanocoatings with easy clean and self-clean capability on a printhead
View Patent ↗A method for producing an inkjet printhead that includes aligning and stacking together an aperture plate and a plurality of jetstack plates; bonding together the aperture plate and plurality of jetstack plates; after the bonding step, depositing a layer of coating material to a surface of the aperture plate by inkjet printing to form a coating on at least a portion of the surface of an outlet surface of the aperture plate; and curing the layer of coating material to form a cured coating. The method may also include forming a second cured coating.
1. A method for producing an inkjet printhead, the method comprising:
aligning and stacking together an aperture plate and a plurality of jetstack sheets;
bonding together the aperture plate and the plurality of jetstack sheets;
after the bonding step, depositing a layer of coating material to a major surface of the aperture plate by inkjet printing to form a coating on at least a portion of an outlet surface of the aperture plate; and
curing the layer of coating material to form a cured coating.
2. The method of claim 1 , wherein the cured coating is configured so that ultra-violet gel ink and solid ink in contact with the cured coating exhibit a sliding angle of 1° to less than 30° and a contact angle larger than 40°.
3. The method of claim 1 , wherein the layer of coating material deposited by inkjet printing is cured at a temperature of 130° C. for 30 minutes to 2 hours and optionally post-cured at a temperature of from 250° C. to 300° C. for 30 minutes to 2 hours.
4. The method of claim 2 , wherein the coating material comprises:
a first isocyanate compound;
a hydroxyl functionalized fluoro-crosslinking material; and
optionally a second isocyanate compound.
5. The method of claim 4 , wherein the first isocyanate compound is selected from the group consisting of diphenylmethane diisocyanate (MDI); toluene diisocyanate (TDI); hexamethylene diisocyanate (HDI); isophorone diisocyanate (IPDI); hydrogenated MDI; tetra-methyl xylene diisocyanate; naphthalene diisocyanate; cyclohexylene diisocyanate; trimethylhexamethylene diisocyanate; bis(4-isocyanatocyclohexyl)methane; uretidione dimers of monomeric diisocynates HDI, IPDI, TDI, and MDI; cyclotrimerized isocyanurates of monomeric diisocynates HDI, IPDI, and TDI; oligomers, polymers, and copolymers containing at least one isocyanate (—NCO) functional group; and mixtures thereof.
6. The method of claim 4 , wherein the hydroxyl functionalized fluoro-crosslinking material is a dihydroxy perfluoropolyether compound having a formula:
HOCH 2 CF 2 O(CF 2 CF 2 O) a (CF 2 C) b CF 2 CH 2 OH
where:
a and b are independently integers in a range of from 0 and 100, provided that at least one of a and b is not 0.
7. The method of claim 4 , wherein the second isocyanate compound is selected from the group consisting of diphenylmethane diisocyanate (MDI); toluene diisocyanate (TDI); hexamethylene diisocyanate (HDI); isophorone diisocyanate (IPDI); hydrogenated MDI; tetra-methyl xylene diisocyanate; naphthalene diisocyanate; cyclohexylene diisocyanate; trimethylhexamethylene diisocyanate; bis(4-isocyanatocyclohexyl)methane; uretidione dimers of monomeric diisocynates HDI, IPDI, TDI, and MDI; cyclotrimerized isocyanurates of monomeric diisocynates like HDI, IPDI, and TDI; oligomers, polymers, and copolymers containing at least one isocyanate (—NCO) functional group; and mixtures thereof.
8. The method of claim 4 , wherein the cured coating exhibits a contact angle of greater than 40° and a sliding angle 1° to less than 30° with solid ink and UV gel ink after the cured coating is soaked in molten wax ink or UV ink at temperatures ranging from 80° C. to 150° C. for 48 hours.
9. The method of claim 2 , wherein the coating material comprises:
a polymer or oligomer containing an isocyanate functional group;
a polymer or oligomer containing a hydroxyl functional group;
a hydroxyl functionalized polymer or oligomer containing at least one polysiloxane unit; and
optionally, a hydroxyl functionalized fluoro-crosslinking material.
10. The method of claim 9 , wherein the polymer or oligomer containing an isocyanate functional group is selected from the group consisting of diphenylmethane diisocyanate (MDI); toluene diisocyanate (TDI); hexamethylene diisocyanate (HDI); isophorone diisocyanate (IPDI); hydrogenated MDI; tetra-methyl xylene diisocyanate; naphthalene diisocyanate; cyclohexylene diisocyanate; trimethylhexamethylene diisocyanate; bis(4-isocyanatocyclohexyl)methane; uretidione dimers of monomeric diisocynates HDI, IPDI, TDI, and MDI; cyclotrimerized isocyanurates of monomeric diisocynates HDI, IPDI, and TDI; and mixtures thereof.
11. The method of claim 9 , wherein the hydroxyl functionalized polymer or oligomer containing at least one polysiloxane unit is a polymer consisting of polysiloxane side-chains on a hydroxyl-functional polyacrylate backbone.
12. The method of claim 9 , wherein the hydroxyl functionalized fluoro-crosslinking material is a dihydroxy perfluoropolyether compound having a formula:
HOCH 2 CF 2 O(CF 2 CF 2 O) a (CF 2 O) b CF 2 CH 2 OH
where:
a and b are independently integers in a range of from 0 and 100, provided that at least one of a and b is not 0.
13. The method of claim 3 , wherein the cured coating layer has a thickness in a range of from 500 to 5,000 nm.
14. The method of claim 1 , wherein the cured coating exhibits a solid ink contact angle of greater than 45°.
15. The method of claim 1 , wherein the cured coating exhibits solid ink and UV gel ink sliding angles of less than 30°.
16. A method for producing an inkjet printhead, the method comprising:
aligning and stacking together an aperture plate and a plurality of jetstack sheets;
bonding together the aperture plate and the plurality of jetstack sheets;
depositing a first coating material on a major surface of the aperture plate around at least one nozzle of the aperture plate;
depositing a second coating material on another portion of the major surface of the aperture plate not being coated by the first coating material; and
curing the first coating material and the second coating material to form a first cured coating and a second cured coating;
wherein the first coating material is deposited by ink jet printing and cured, followed by the second coating material being deposited by inkjet printing and cured.
17. The method of claim 16 , wherein the first cured coating is configured so that ultra-violet gel ink and solid ink in contact with the first cured coating exhibit a sliding angle of 1° to less than 30° and a contact angle larger than 45°.
18. The method of claim 16 , wherein the second cured coating is configured so that ultra-violet gel ink and solid ink in contact with the second cured coating exhibit a sliding angle of 1° to less than 30° and a contact angle larger than 40°.
19. The method of claim 16 , wherein the first coating material comprises:
a first isocyanate compound;
a hydroxyl functionalized fluoro-crosslinking material; and
optionally a second isocyanate compound.
20. The method of claim 19 , wherein the first isocyanate compound is selected from the group consisting of diphenylmethane diisocyanate (MDI); toluene diisocyanate (TDI); hexamethylene diisocyanate (HDI); isophorone diisocyanate (IPDI); hydrogenated MDI; tetra-methyl xylene diisocyanate; naphthalene diisocyanate; cyclohexylene diisocyanate; trimethylhexamethylene diisocyanate; bis(4-isocyanatocyclohexyl)methane; uretidione dimers of monomeric diisocynates HDI, IPDI, TDI, and MDI; cyclotrimerized isocyanurates of monomeric diisocynates like HDI, IPDI, and TDI; oligomers, polymers, and copolymers containing at least one isocyanate (—NCO) functional group; and mixtures thereof.
21. The method of claim 19 , wherein the hydroxyl functionalized fluoro-crosslinking material is a dihydroxy perfluoropolyether compound having a formula:
HOCH 2 CF 2 O(CF 2 CF 2 O) a (CF 2 O) b CF 2 CH 2 OH
where:
a and b are independently integers in a range of from 0 and 100, provided that at least one of a and b is not 0.
22. The method of claim 16 , wherein the second coating material comprises:
a polymer or oligomer containing an isocyanate functional group;
a polymer or oligomer containing a hydroxyl functional group;
a hydroxyl functionalized polymer or oligomer containing at least one polysiloxane unit; and
optionally, a hydroxyl functionalized fluoro-crosslinking material.
23. The method of claim 22 , wherein the polymer or oligomer containing an isocyanate functional group is selected from the group consisting of diphenylmethane diisocyanate (MDI); toluene diisocyanate (TDI); hexamethylene diisocyanate (HDI); isophorone diisocyanate (IPDI); hydrogenated MDI; tetra-methyl xylene diisocyanate; naphthalene diisocyanate; cyclohexylene diisocyanate; trimethylhexamethylene diisocyanate; bis(4-isocyanatocyclohexyl)methane; uretidione dimers of monomeric diisocynates HDI, IPDI, TDI, and MDI; cyclotrimerized isocyanurates of monomeric diisocynates HDI, IPDI, and TDI; and mixtures thereof.
24. The coating of claim 22 , wherein the hydroxyl functionalized polymer or oligomer containing at least one polysiloxane unit is a polymer consisting of polysiloxane side-chains on a hydroxyl-functional polyacrylate backbone.
25. The coating of claim 22 , wherein the hydroxyl functionalized fluoro-crosslinking material is a dihydroxy perfluoropolyether compound having a formula:
HOCH 2 CF 2 O(CF 2 CF 2 O) a (CF 2 O) b CF 2 CH 2 OH
where:
a and h are independently integers in a range of from 0 and 100, provided that at least one of a and b is not 0.
26. The method of claim 16 , wherein the first and the second cured coating layers have a thickness in a range of from 500 to 5,000 nm.