Colorless digital primer for digital printing

Patent metadata

Field	Value
Publication number	US-9639011-B2
Application number	US-201314894078-A
Country	US
Kind code	B2
Filing date	Jun 28, 2013
Priority date	Jun 28, 2013
Publication date	May 2, 2017
Grant date	May 2, 2017

Abstract

A colorless digital primer for digital printing includes a colorless paste. The colorless paste includes a non-polar carrier fluid, and a resin swollen in the non-polar carrier fluid. The resin is present in the paste in an amount ranging from about 20% (w/w) to about 50% (w/w). A solid polar compound is dispersed in the resin. The solid polar compound is selected from the group consisting of a cellulose microcrystalline powder, dextrin, maltose monohydrate, polyacrylic acid, polyvinyl alcohol, a styrene maleic anhydride copolymer, a bismaleimide oligomer, sucrose, sucrose octaacetate, sucrose benzoate, and combinations thereof. The solid polar compound is present in an amount up to 60 wt. % of solids in the colorless paste.

First claim

What is claimed is:

1. A digital method for priming a substrate for subsequently receiving liquid electrophotographic (LEP) ink, the digital method comprising:
selecting a colorless primer, including:
a resin swollen with a non-polar carrier fluid;
a solid polar compound dispersed in the swollen resin, the solid polar compound being selected from the group consisting of a cellulose microcrystalline powder, dextrin, maltose monohydrate, polyacrylic acid, polyvinyl alcohol, a styrene maleic anhydride copolymer, a bismaleimide oligomer, sucrose, sucrose octaacetate, sucrose benzoate, and combinations thereof;
a charge adjuvant; and
additional non-polar carrier fluid present in an amount such that a total solids content of the colorless primer ranges from about 1% (w/w) to about 5% (w/w); and

applying the colorless primer directly to a surface of the substrate.

2. The digital method as defined in claim 1 wherein the styrene maleic anhydride copolymer is selected from i) styrene maleic anhydride resin, cumene end-capped and ii) a copolymer of styrene and dimethyl amino propylamine maleimide.

3. The digital method as defined in claim 1 , further comprising selecting the substrate from the group consisting of corona treated polymeric (bi-oriented polypropylene), a coated paper, and an uncoated paper.

4. The digital method as defined in claim 1 wherein the applying of the colorless primer is accomplished using liquid electrophotographic printing.

5. The digital method as defined in claim 1 wherein the selected colorless primer further includes a charge director.

6. The digital method as defined in claim 1 wherein the selected colorless primer includes:
an isoparaffinic hydrocarbon as the non-polar carrier fluid;
any of an ethylene methacrylic copolymer or an ethylene acrylic copolymer as the resin;
the polyacrylic acid as the solid polar compound; and
aluminum stearate as the charge adjuvant.

7. A colorless digital primer, comprising:
a colorless paste, including:
a non-polar carrier fluid; and
a resin swollen in the non-polar carrier fluid, the resin present in the paste in an amount ranging from about 20% (w/w) to about 50% (w/w); and
a solid polar compound dispersed in the resin, the solid polar compound being selected from the group consisting of a cellulose microcrystalline powder, dextrin, maltose monohydrate, polyacrylic acid, polyvinyl alcohol, a styrene maleic anhydride copolymer, a bismaleimide oligomer, sucrose, sucrose octaacetate, sucrose benzoate, and combinations thereof, and the solid polar compound being present in an amount up to 60 wt. % of solids in the colorless paste.

8. The colorless digital primer as defined in claim 7 wherein the colorless digital primer is in a concentrated form having a total solids content ranging from about 20% (w/w) to less than 100% (w/w).

9. The colorless digital primer as defined in claim 7 , further comprising additional non-polar carrier fluid so that a total solids content in the colorless primer ranges from about 1% (w/w) to about 5% (w/w).

10. The colorless digital primer as defined in claim 7 wherein the styrene maleic anhydride copolymer is selected from i) styrene maleic anhydride resin, cumene end-capped and ii) a copolymer of styrene and dimethyl amino propylamine maleimide.

11. A method of making a colorless digital primer, comprising:
selecting a solid polar compound from the group consisting of a cellulose microcrystalline powder, dextrin, maltose monohydrate, polyacrylic acid, polyvinyl alcohol, a styrene maleic anhydride copolymer, a bismaleimide oligomer, sucrose, sucrose octaacetate, sucrose benzoate, and combinations thereof;
adding the solid polar compound to a colorless paste including a non-polar carrier fluid and a resin; and
grinding the solid polar compound and the colorless paste to disperse the solid polar compound in the resin of the colorless paste.

12. The method as defined in claim 11 wherein selecting the solid polar compound includes selecting the styrene maleic anhydride copolymer from i) styrene maleic anhydride resin, cumene end-capped, and ii) a copolymer of styrene and dimethyl amino propylamine maleimide.

13. The method as defined in claim 11 , further comprising pre-grinding the solid polar compound to reduce a particle size of the solid polar compound to be within a range of about 30 nm to about 300 nm.

14. The method as defined in claim 11 , further comprising:
adding a charge adjuvant during the grinding;
diluting the colorless paste with additional non-polar carrier fluid; and
adding a charge director after the grinding and the diluting.

15. The method as defined in claim 11 wherein the grinding is accomplished at a temperature ranging from about 25° C. to about 40° C. for a time ranging from about 12 hours to about 48 hours.

Assignees

• Hewlett Packard Indigo Bv

Inventors

• Ron Hannoch
• Tzomik Inna
• Skvirsky Daniel

Classifications

• G03G5/142 Primary

  Inert intermediate layers · CPC title

• G03G7/0026

  being macromolecular · CPC title

• G03G9/13

  characterised by polymer components · CPC title

• G03G9/125

  characterised by the liquid · CPC title

• C09D11/14

  based on carbohydrates · CPC title