IP Library Granted Patent US 9,090,791
Granted Patent B2
US 9,090,791 · App. 13/909,975 · Granted Jul 28, 2015

Mixtures of ester of tartaric acid and ester of citric acid as amorphous materials for phase change inks

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Quick Facts
Patent No.
US 9,090,791
App. No.
13/909,975
Granted
Jul 28, 2015
Kind
B2
Abstract

The disclosure provides amorphous materials comprising mixtures of ester of tartaric acid and ester of citric acid, which are suitable for phase change inks.

Claims (33)

1. An amorphous material for use as a component of a phase change ink, the amorphous material comprising a mixture of:

an ester of tartaric acid; and

an ester of citric acid,

wherein the amorphous material has a glass transition temperature of from about −20° C. to about 50° C.

2. The amorphous material of claim 1 , wherein the amorphous material has a glass transition temperature of from about −17° C. to about 40° C.

3. The amorphous material of claim 1 , wherein the amorphous material has a viscosity of from about 1 cps to about 200 cps at a temperature from about 100 to about 140° C.

4. The amorphous material of claim 1 , wherein the mol % ratio of the ester tartaric acid to the ester citric acid is from about 10:90 to about 90:10.

5. The amorphous material of claim 1 , wherein the mol % ratio of the ester of tartaric acid to the ester of citric acid is from about 25:75 to about 75:25.

6. The amorphous material of claim 1 , wherein the ester of tartaric acid has a formula of

wherein each R 1 and R 2 is independently alkyl, aryl or heteroaryl group, and further wherein the tartaric acid backbone is selected from L-(+)-tartaric acid, D-(−)-tartaric acid, DL-tartaric acid, mesotartaric acid, and mixtures thereof.

7. The amorphous material of claim 6 , wherein each R 1 and R 2 is alkyl group.

8. The amorphous material of claim 7 , wherein each R 1 and R 2 is cyclohexyl group.

9. The amorphous material of claim 6 , wherein the ester of tartaric acid 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.

10. The amorphous material of claim 1 , wherein the ester of citric acid has a formula of

wherein each R 3 , R 4 and R 5 is independently alkyl, aryl or heteroaryl group.

11. The amorphous material of claim 10 , wherein each R 3 , R 4 and R 5 is cyclohexyl group.

12. The amorphous material of claim 10 , wherein the ester of citric acid selected from the group consisting of tris(3-phenylpropyl) citrate, tris(2-phenoxyethyl) citrate, tricyclohexyl citrate, tribenzyl citrate, tris(3,5,5-trimethylhexyl) citrate, tri-DL-menthyl citrate, tri-L-menthyl citrate, tris(4-tert-butylcyclohexyl) citrate, tris(2-phenylethyl) citrate, tricyclopentyl citrate and mixtures thereof.

13. An amorphous material, for use as a component of an phase change ink, the amorphous material comprising a mixture of:

an ester of tartaric acid having a formula of

wherein each R 1 and R 2 is independently alkyl, aryl or heteroaryl group, and further wherein the tartaric acid backbone is selected from L-(+)-tartaric acid, D-(−)-tartaric acid, DL-tartaric acid, mesotartaric acid, and mixtures thereof; and

an ester of citric acid having a formula of

wherein each R 3 , R 4 and R 5 is independently selected from the group consisting of

wherein the amorphous component has a glass transition temperature of from about −20° C. to about 50° C.

14. The amorphous material of claim 13 , wherein each R 1 and R 2 is cyclohexyl group.

15. The amorphous material of claim 13 , wherein each R 3 , R 4 and R 5 is cyclohexyl group.

16. The amorphous material of claim 13 , wherein the mol % ratio of the ester of tartaric acid to the ester of citric acid is from about 10:90 to about 90:10.

17. An amorphous material for use as a component of an phase change ink, the amorphous material comprising a mixture of:

an ester of tartaric acid 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; and

an ester of citric acid selected from the group consisting of tris(3-phenylpropyl) citrate, tris(2-phenoxyethyl) citrate, tricyclohexyl citrate, tribenzyl citrate, tris(3,5,5-trimethylhexyl) citrate, tri-DL-menthyl citrate, tri-L-menthyl citrate, tris(4-tert-butylcyclohexyl) citrate, tris(2-phenylethyl) citrate, tricyclopentyl citrate and mixtures thereof,

wherein the amorphous component has a glass transition temperature of from about −20° C. to about 50° C.

18. The amorphous material of claim 17 , wherein the ester of tartaric acid comprises dicyclohexyl L-tartrate.

19. The amorphous material of claim 17 , wherein the ester of citric acid comprises tricyclohexyl citrate.

20. The amorphous material of claim 17 , wherein the mol % ratio of the ester of tartaric acid to the ester of citric acid is from about 10:90 to about 90:10.

Assignments (10)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2025
From: XEROX CORPORATION
To: GENESEE VALLEY INNOVATIONS, LLC
Reel/Frame 073842/0479 →
SECOND LIEN NOTES PATENT SECURITY AGREEMENT Recorded Jul 2, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 071785/0550 →
FIRST LIEN NOTES PATENT SECURITY AGREEMENT Recorded Apr 11, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 070824/0001 →
SECURITY INTEREST Recorded Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT RF 064760/0389 Recorded Feb 13, 2024
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: XEROX CORPORATION
Reel/Frame 068261/0001 →
SECURITY INTEREST Recorded Nov 20, 2023
From: XEROX CORPORATION
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 065628/0019 →
SECURITY INTEREST Recorded Jun 22, 2023
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 064760/0389 →
RELEASE OF SECURITY INTEREST IN PATENTS AT R/F 062740/0214 Recorded May 18, 2023
From: CITIBANK, N.A., AS AGENT
To: XEROX CORPORATION
Reel/Frame 063694/0122 →
SECURITY INTEREST Recorded Nov 10, 2022
From: XEROX CORPORATION
To: CITIBANK, N.A., AS AGENT
Reel/Frame 062740/0214 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 4, 2013
From: MORIMITSU, KENTARO; GOREDEMA, ADELA; CHOPRA, NAVEEN
To: XEROX CORPORATION
Reel/Frame 030545/0477 →