Performance of LED-curable digital ink

Patent metadata

Field	Value
Publication number	US-12297360-B2
Application number	US-202117995593-A
Country	US
Kind code	B2
Filing date	Apr 9, 2021
Priority date	Apr 9, 2020
Publication date	May 13, 2025
Grant date	May 13, 2025

Abstract

Digital ink formulations that cure by the application of light emitting diode (LED) energy are described. Also described are methods of bonding the LED-curable formulations onto substrates.

First claim

What is claimed is:

1. A formulation for printing to a substrate, consisting essentially of:
a combination of monomers, the combination consists of:
at least one mono-acrylated monomer,
at least one di-acrylated monomer,
at least one tri-acrylated monomer, and
at least one polyalkoxylated acrylate monomer;

at least one photoinitiator;
at least one pigment dispersion;
at least one leveling agent; and
at least one inhibitor;
wherein a weight ratio of the di-acrylated monomer to the mono-acrylated monomer is from about 3.3 to about 6.0;
wherein a weight ratio of the di-acrylated monomer to the tri-acrylated monomer is from about 4.5 to about 8.0; and
wherein the formulation is an LED-curable digital ink.

2. The formulation of claim 1 , wherein the mono-acrylated monomer is selected from the group consisting of lauryl acrylate, caprolactam acrylate, isodecyl acrylate, tetra hydrofurfuryl acrylate, cyclic trimethylolpropane formyl acrylate, 4-tert butylcyclohexyl acrylate, and any combination thereof.

3. The formulation of claim 1 , wherein the di-acrylated monomer is selected from the group consisting of 1,6 hexanediol ethoxylated diacrylate, 1,6 hexanediol diacrylate (HD), 1,10 deconediol diacrylate, dipropylene glycol diacrylate, tripropylene glycol diacrylate, and any combination thereof.

4. The formulation of claim 1 , wherein the tri-acrylated monomer is selected from the group consisting of trimethylolpropane triacrylate, trimethylolpropane (EO)3 triacrylate, trimethylolpropane (EO)6 triacrylate, trimethylolpropane (EO)9 triacrylate, trimethylolpropane (EO)15 triacrylate, pentaerythritol triacrylate, and any combination thereof.

5. The formulation of claim 1 , wherein the formulation is LED cured at a power of from about 8 watts to about 20 watts and a wavelength of from about 380 nm to about 400 nm.

6. The formulation of claim 1 , wherein the substrate is selected from the group consisting of fabric, paper, wood, metal, glass, plastic, and any combination thereof.

7. The formulation of claim 1 , wherein the combination of monomers is radically curable.

8. A method of bonding a digital ink formulation onto a substrate, comprising:
at least partially disposing a digital ink formulation having a pattern or an indicia onto a substrate,
wherein the digital ink formulation consisting essentially of combination of monomers, the combination consists of:
at least one mono-acrylated monomer;
at least one di-acrylated monomer; and
at least one tri-acrylated monomer;
at least one polyalkoxylated acrylate monomer,

at least one photoinitiator;
at least one pigment dispersion;
at least one leveling agent; and
at least one inhibitor;
wherein a weight ratio of the di-acrylated monomer to the mono-acrylated monomer is from about 3.3 to about 6.0;
wherein a weight ratio of the di-acrylated monomer to the tri-acrylated monomer is from about 4.5 to about 8.0; and
wherein an LED curing of the digital ink formulation on the substrate at least partially transfers the pattern or the indicia to the substrate to provide a modified substrate.

9. The method of claim 8 , wherein the at least partially disposing comprises printing on the substrate.

10. The method of claim 8 , wherein the substrate is selected from the group consisting of fabric, paper, wood, metal, glass, plastic, and any combination thereof.

11. The method of claim 8 , wherein the substrate is a fabric.

12. The method of claim 8 , wherein the digital ink formulation enhances at least one of washing testing performance, dry crock testing performance, wet crock testing performance, and leaching testing performance.

13. The method of claim 8 , wherein the formulation is LED cured at a power of from about 8 watts to about 20 watts and a wavelength of about 380 nm to about 400 nm.

14. The method of claim 8 , wherein the curing of the digital ink formulation is characterized by a total relative enthalpy of at least 90 J/kg.

15. The method of claim 8 , wherein the cured digital ink formulation has a total amount of residual monomer of no more than 500 ppm.

16. The method of claim 8 , wherein the cured digital ink formulation has a total amount of residual monomer of no more than 200 ppm.

17. An article comprising a fabric substrate modified according to the method of claim 8 .

18. The formulation of claim 1 , wherein the at least one di-acrylated monomer has a molecular weight of at least 225 g/mol, an acid value of less than 0.7 kOH/g, and a viscosity from about 0.5 to about 30 mPa at temperature of 25° C.

19. The formulation of claim 1 , wherein the at least one tri-acrylated monomer has a molecular weight of at least 275 g/mol, an acid value of less than 0.4 kOH/g, and a viscosity from about 20 to about 150 mPa at temperature of 25° C.

Assignees

• Avery Dennison Retail Information Services Llc

Inventors

• Sharma Pramod
• Roberts Shawn
• Deininger James
• Pearce Michelle

Classifications

• D06P5/2005

  Treatments with alpha, beta, gamma or other rays, e.g. stimulated rays · CPC title

• D06P1/5257

  (Meth)acrylic acid · CPC title

• C09D133/08

  Homopolymers or copolymers of acrylic acid esters · CPC title

• D06P5/30

  Ink jet printing · CPC title

• C09D11/322

  Pigment inks · CPC title