Granted Patent B2

US 9,738,811 · App. 13/975,933 · Granted Aug 22, 2017

Abstract

Claims (65)

1. A phase change ink composition comprising: a phase change carrier composition comprising:

a wax; and

a wax-soluble near-infrared (NIR) dye having an absorption maximum in the wavelength region from about 700 nm to about 1400 nm, wherein the wax-soluble NIR dye is represented by formula (II), (III), or (IV), a tautomer thereof, or a salt thereof, wherein formulas (II), (III), and (IV) are:

wherein R 3 , R 4 , R 7 , R 8 , R 9 , or R 10 is independently a cyclic group-containing residue comprising at least one cyclic group selected from the group consisting of (a) a substituted or unsubstituted heterocyclic group comprising at least one of N, S, or O, (b) a substituted or unsubstituted cycloalkyl group, (c) a substituted or unsubstituted aryl group, and (d) a substituted or unsubstituted aralkyl group;

wherein at least one of R 3 or R 4 , comprises a substituted or unsubstituted perimidine group,

wherein at least one of R 7 or R 8 comprises a substituted or unsubstituted perimidine group,

wherein at least one of R 9 or R 10 comprises a substituted or unsubstituted perimidine group,

wherein each of R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 independently comprises between about 10 and about 150 carbon atoms;

wherein each of R 5 and R 6 is independently selected from the group consisting of H and alkyl groups having from 1 to 6 carbon atoms; and

wherein X is:

 and

wherein n is 1 to 5, wherein the phase change ink composition is in a solid phase at room temperature.

2. The phase change ink composition of claim 1 , wherein the wax-soluble NIR dye has an absorption maximum in the wavelength region from about 700 nm to about 900 nm.

3. The phase change ink composition of claim 1 , wherein the wax is a polyethylene wax having: a molecular weight between about 200 Da and about 5,000 Da.

4. The phase change ink composition of claim 1 , comprising about 0.1 wt. % and about 80 wt. % of the wax relative to the total weight of the phase change ink composition, wherein an ink droplet of the phase change ink composition spreads upon exposure to infrared radiation.

5. The phase change ink composition of claim 1 , comprising between about 0.01 wt. % and about 20 wt. % of the wax-soluble NIR dye relative to the total weight of the phase change ink composition.

6. The phase change ink composition of claim 1 , wherein each of R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 comprises a substituted or unsubstituted perimidine group.

7. The phase change ink composition of claim 1 , wherein at least one of R 3 , R 4 , R 7 , R 8 , R 9 , R 10 comprises at least one linear alkyl group having 5 to 50 carbon atoms in addition to the cyclic group-containing residue.

8. The phase change ink composition of claim 1 , wherein:

(i) R 3 or R 4 is independently selected from the group consisting of

(ii) R 5 or R 6 is independently selected from the group consisting of H and alkyl groups having from 1 to 6 carbon atoms;

(iii) R 7 or R 8 is independently selected from the group consisting of

(iv)) R 9 or R 10 is independently selected from the group consisting of

9. The phase change ink composition of claim 1 , wherein the phase change carrier composition comprises:

(a) a urethane resin that is the reaction product of the reaction of at least one first alcohol and a first isocyanate, the alcohol being selected from the group consisting of hydroabietyl alcohol, octylphenol ethoxylate, and octadecyl alcohol; and/or

(b) a mixed urethane/urea resin that is the reaction product of at least one second alcohol, a second isocyanate, and at least one monoamine; and

(c) at least: one monoamide; and

(d) at least one polyethylene wax.

10. The phase change ink composition of claim 9 , wherein the second alcohol is selected from the group consisting of hydroabietyl alcohol, octylphenol ethoxylate and octadecyl alcohol.

11. The phase change ink composition of claim 9 , wherein the second isocyanate is selected from the group consisting of a monoisocyanate, a diisocyanate, a triisocyanate, a copolymer of a diisocyanate, and a copolymer of a triisocyanate.

12. The phase change ink composition of claim 9 , wherein the second isocyanate is isophorone diisocyanate.

13. The phase change ink composition of claim 9 , wherein the monoamine is selected from the group consisting of an aliphatic monoamine, an aromatic monoamine, an aliphatic/aromatic monoamine, a fused ring system monoamine, and a hydroxyl/amino containing compound.

14. The phase change ink composition of claim 9 , wherein the monoamine is octadecyl amine.

15. The phase change ink composition of claim 9 , wherein the monoamide is stearyl stearamide.

16. A method for producing a layer of a phase change ink on the surface of a substrate, which comprises:

(1) employing in a printing apparatus a phase change ink composition in the solid phase comprising an admixture of (a) a phase change carrier composition and (b) a wax-soluble near-infrared (NIR) dye having an absorption maximum in the wavelength region from about 700 nm to about 1400 nm;

wherein the phase change carrier composition comprises (i) a urethane resin that is the reaction product of at least one first alcohol and a first isocyanate; and/or (ii) a urethane/urea resin that is the reaction product of at least one second alcohol, a second isocyanate and at least one monoamine; and (iii) at least one monoamide; and (iv) at least one polyethylene wax; and

wherein the wax-soluble NIR dye is represented by formula (II), (III), or (IV), a tautomer thereof, or a salt thereof, wherein formulas (II), (III), and (IV) are:

wherein each of R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 is independently a cyclic group-containing residue comprising at least one cyclic group selected from the group consisting of (a) a substituted or unsubstituted heterocyclic group comprising at least one of N, S, or O, (b) a substituted or unsubstituted cycloalkyl group, (c) a substituted or unsubstituted aryl group, and (d) a substituted or unsubstituted aralkyl group;

wherein at least one of R 3 or R 4 comprises a substituted or unsubstituted perimidine group,

wherein at least one of R 7 or R 8 comprises a substituted or unsubstituted perimidine group,

wherein at least one of R 9 or R 10 comprises a substituted or unsubstituted perimidine group,

wherein each of R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 independently comprises between about 10 and about 150 carbon atoms;

wherein each of R 5 and R 6 is independently selected from the group consisting of H and alkyl groups having from 1 to 6 carbon atoms; and

wherein X is:

 and

wherein n is 1 to 5, and wherein the phase change ink composition is in a solid phase at room temperature;

(2) applying the phase change ink composition in a desired pattern to an intermediate transfer surface;

(3) transferring the desired pattern of the phase change ink composition to the surface of the substrate.

17. A near-infrared print comprising: a substrate and a phase change ink composition disposed on a surface of the substrate, wherein the phase change ink composition comprises a phase change carrier composition comprising a wax and a wax-soluble near-infrared (NIR) dye having an absorption maximum in the wavelength region from about 700 nm to about 1400 nm, and wherein the wax-soluble NIR dye is represented by formula (II), (III), or (IV) a tautomer thereof, or a salt thereof, wherein formulas (II), (III), and (IV) are:

wherein R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 is independently a cyclic group-containing residue comprising at least one cyclic group selected from the group consisting of (a) a substituted or unsubstituted heterocyclic group comprising at least one of N, S, or O, (b) a substituted or unsubstituted cycloalkyl group, (c) a substituted or unsubstituted aryl group, and (d) a substituted or unsubstituted aralkyl group;

wherein at least one of R 3 or R 4 comprises a substituted or unsubstituted perimidine group,

wherein at least one of R 7 or R 8 comprises a substituted or unsubstituted perimidine group,

wherein at least one of R 9 or R 10 comprises a substituted or unsubstituted perimidine group,

wherein each of R 3 , R 4 , R 7 , R 8 , R 9 , and R 10 independently comprises between about 10 and about 150 carbon atoms;

wherein each of R 5 and R 6 is independently selected from the group consisting of H and alkyl groups having from 1 to 6 carbon atoms; and

wherein X is;

wherein n is 1 to 5, wherein the phase change ink composition is in a solid phase at room temperature.

18. The near-infrared print of claim 17 , wherein the print is prepared by a method comprising:

(1) providing an admixture of (a) the phase change carrier composition; and (b) the wax-soluble NIR dye;

(2) transferring the solid phase, phase change ink composition to a phase change ink applicator;

(3) raising the operating temperature of the applicator to a level whereby a liquid phase, phase change ink composition is formed;

(4) providing the substrate in proximity to the applicator;

(5) applying a predetermined pattern of the liquid phase, phase change ink composition to the surface of the substrate; and

(6) lowering the temperature of the applied liquid phase, phase change ink composition to form a solid phase, phase change ink pattern on the substrate.

Assignments (10)