IP Library Granted Patent US 10,416,585
Granted Patent B2
US 10,416,585 · App. 15/833,211 · Granted Sep 17, 2019

Electrostatic ink compositions

Inventors: Gil Bar-Haim (Nes Ziona, IL); Alina Grishman (Nes Ziona, IL)
Assignee: HP Indigo B.V.
G03G9/135C09D11/03C09D11/106G03G9/08G03G9/0804G03G9/0808G03G9/09733G03G9/12G03G9/132G03G13/10
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Quick Facts
Patent No.
US 10,416,585
App. No.
15/833,211
Granted
Sep 17, 2019
Kind
B2
Abstract

Herein is disclosed an electrostatic ink composition, wherein the composition is formable by combining: chargeable particles comprising a resin comprising a polymer having acidic side groups, and a cyclic anhydride. Also disclosed herein is a method of forming an electrostatic ink composition, and a method of electrostatic printing.

Claims (30)

1. An electrostatic ink composition, wherein the composition is formable by combining:

chargeable particles comprising a resin comprising a polymer having acidic side groups which are free of ester groups, and further comprising a polymer having ester side groups,

a cyclic anhydride, wherein the cyclic anhydride is selected from benzophenone tetracarboxylic dianhydride, 3,3-dimethylglutaric anhydride, diglycolic anhydride, or bromomaleic anhydride, and

a carrier liquid, wherein the chargeable particles are dispersed in the carrier liquid.

2. The electrostatic ink composition according to claim 1 , wherein the cyclic anhydride constitutes from 0.1 wt % to 10 wt % of the solids of the electrostatic ink composition.

3. The electrostatic ink composition according to claim 1 , wherein the cyclic anhydride constitutes from 0.5 wt % to 3 wt % of the solids of the electrostatic ink composition.

4. The electrostatic ink composition according to claim 1 , wherein the electrostatic ink composition further comprises a charge director.

5. The electrostatic ink composition according to claim 4 , wherein the charge director comprises a sulfosuccinate moiety of the general formula [R 1′ —O—C(O)CH 2 CH(SO 3 − )C(O)—O—R 2 ′], where each of R 1 ′ and R 2 ′ is an alkyl group.

6. The electrostatic ink composition according to claim 5 , wherein each of R 1′ and R 2′ independently is a C 6-25 alkyl.

7. The electrostatic ink composition according to claim 1 , wherein the polymer having acidic side groups is a co-polymer of (ii) a first monomer having acidic side groups selected from acrylic or methacrylic acid and (iii) a second monomer which is an alkylene monomer selected from ethylene and propylene.

8. The electrostatic ink composition according to claim 1 , wherein the polymer having ester side groups is a co-polymer of a first monomer having ester side groups, a second monomer having acidic side groups, and a third monomer which is an alkylene monomer.

9. The electrostatic ink composition according to claim 8 , wherein the first monomer constitutes 8% to 12% by weight of the co-polymer, the second monomer constitutes 8% to 12% by weight of the co-polymer, and the third monomer constitutes the remaining weight of the co-polymer.

10. A method of forming the electrostatic ink composition of claim 1 , the method comprising combining the chargeable particles and the cyclic anhydride.

11. The electrostatic ink composition according to claim 1 , wherein the cyclic anhydride is bromomaleic anhydride.

12. A method of electrostatic printing, the method comprising:

providing the electrostatic ink composition according to claim 1 ,

contacting the electrostatic ink composition with a latent electrostatic image on a surface to create a developed image; and

transferring the developed image to a print substrate.

13. An electrostatic ink composition, wherein the composition is formable by combining:

chargeable particles comprising a resin comprising a polymer having acidic side groups which are free of ester groups, and further comprising a polymer having ester side groups, and

bromomaleic anhydride.

14. The electrostatic ink composition according to claim 13 , wherein the cyclic anhydride constitutes from 0.1 wt % to 10 wt % of the solids of the electrostatic ink composition.

15. The electrostatic ink composition according to claim 13 , wherein the cyclic anhydride constitutes from 0.5 wt % to 3 wt % of the solids of the electrostatic ink composition.

16. The electrostatic ink composition according to claim 13 , wherein the electrostatic ink composition further comprises a charge director.

17. The electrostatic ink composition according to claim 16 , wherein the charge director comprises a sulfosuccinate moiety of the general formula [R 1′ —O—C(O)CH 2 CH(SO 3 − )C(O)—O—R 2′ ], where each of R 1′ and R 2′ is an alkyl group.

18. The electrostatic ink composition according to claim 17 , wherein each of R 1′ and R 2′ independently is a C 6-25 alkyl.

19. The electrostatic ink composition according to claim 13 , wherein the polymer having acidic side groups is a co-polymer of (ii) a first monomer having acidic side groups selected from acrylic or methacrylic acid and (iii) a second monomer which is an alkylene monomer selected from ethylene and propylene.

20. The electrostatic ink composition according to claim 13 , wherein the composition further comprises a carrier liquid and the chargeable particles comprising the resin comprising the polymer having acidic side groups are dispersed in the liquid carrier.

21. The electrostatic ink composition according to claim 13 , wherein the polymer having ester side groups is a co-polymer of a first monomer having ester side groups, a second monomer having acidic side groups, and a third monomer which is an alkylene monomer.

22. The electrostatic ink composition according to claim 21 , wherein the first monomer constitutes 8% to 12% by weight of the co-polymer, the second monomer constitutes 8% to 12% by weight of the co-polymer, and the third monomer constitutes the remaining weight of the co-polymer.

Assignments (3)
CHANGE OF NAME Recorded Dec 13, 2017
From: HEWLETT-PACKARD INDIGO, B.V.
To: HP INDIGO B.V.
Reel/Frame 044728/0276 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2017
From: BAR-HAIM, GIL; GRISHMAN, ALINA
To: HEWLETT-PACKARD INDIGO B.V.
Reel/Frame 044314/0574 →
CHANGE OF NAME Recorded Dec 6, 2017
From: HEWLETT-PACKARD INDIGO B.V.
To: HP INDIGO B.V.
Reel/Frame 044723/0759 →
Continuity (2)
Continuation 15109777
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