Phase change ink components and methods of making the same

• US 8,308,859 B1
• Filed: 04/27/2011
• Issued: 11/13/2012
• Est. Priority Date: 04/27/2011
• Status: Expired due to Fees

• Current Assignee: Xerox Corporation (Xerox Holdings Corp.)
• Original Assignee: Xerox Corporation (Xerox Holdings Corp.)
• Inventors: Belelie, Jennifer L., Morimitsu, Kentaro, Chopra, Naveen, Tracy, Corey, Drappel, Stephan V., Odell, Peter G.
• Primary Examiner(s): Mayes, Melvin C
• Assistant Examiner(s): Qian, Yun
• Application Number:
  US13/095,591
• Publication Number:
  US 20120272860A1
• Time in Patent Office: 566 Days
• Field of Search: None
• US Class Current: 106/31.29
• CPC Class Codes: C09D 11/34 Hot-melt inks
• CPC Class Codes: C09D 11/38 characterised by non-macromolecular additives other than solvents, pigments or dyes

Abstract

A solid ink composition comprising an amorphous component, a crystalline material, and optionally, a colorant, which are suitable for ink jet printing, including printing on coated paper substrates, and methods for making the same. In embodiments, the crystalline and amorphous components are synthesized from an esterification reaction of tartaric acid with an alcohol.

Claims

1. A method of preparing a phase change ink comprising:

providing at least a crystalline component in a molten state;

providing at least an amorphous component in a molten state;

stirring the crystalline and amorphous component together to form a mixture for a phase change ink; and

cooling the mixture for the phase change ink, wherein the crystalline and amorphous components are esters of tartaric acid.

2. The method of claim 1, wherein a colorant is further added to the mixture before cooling.

3. The method of claim 1, wherein the crystalline and amorphous components are present in a weight ratio of from about 50:

50 to about 95;

5.

4. The method of claim 3, wherein the crystalline and amorphous components are present in a weight ratio of from about 65:

35 to about 90;

10.

5. The method of claim 4, wherein the crystalline and amorphous components are present in a weight ratio of from about 70:

30 to about 90;

10.

6. The method of claim 1, wherein the amorphous component is selected from the group consisting of di-L-menthyl L-tartrate, di-DL-menthyl L-tartrate, di-L-menthyl DL-tartrate, di-DL-menthyl DL-tartrate, and any stereoisomers and mixtures thereof.

7. The method of claim 1, wherein the crystalline component is selected from the group consisting of dibenzyl L-tartrate, diphenethyl L-tartrate, bis(3-phenyl-1-propyl) L-tartrate, bis(2-phenoxyethyl) L-tartrate, diphenyl L-tartrate, bis(4-methylphenyl) L-tartrate, bis(4-methoxylphenyl) L-tartrate, bis(4-methylbenzyl) L-tartrate, bis(4-methoxylbenzyl) L-tartrate, dicyclohexyl L-tartrate, bis(4-tert-butylcyclohexyl) L-tartrate, and any stereoisomers and mixtures thereof.

8. A method of preparing a phase change ink comprising:

providing at least a crystalline component in a molten state;

providing at least an amorphous component in a molten state;

stirring the crystalline and amorphous component together to form a mixture for a phase change ink; and

cooling the mixture for the phase change ink, wherein the crystalline and amorphous components are esters of tartaric acid produced by an esterification reaction with an alcohol.