IP Library Granted Patent US 7,704,312
Granted Patent B2
US 7,704,312 · App. 12/094,790 · Granted Apr 27, 2010

Non-aqueous pigment dispersions containing specific dispersion synergists

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Quick Facts
Patent No.
US 7,704,312
App. No.
12/094,790
Granted
Apr 27, 2010
Kind
B2
Abstract

A non-aqueous pigment dispersion includes a color pigment, a polymeric dispersant, and a dispersion synergist in a dispersion medium wherein the dispersion synergist is represented by Formula (I): wherein AR 1 and AR 2 represent a substituted or unsubstituted aromatic group, and R represents a substituted or unsubstituted aliphatic group, with the proviso that one of R, AR 1 , and AR 2 contains at least one carboxylate anion and that the molecular weight of the anionic part of the dispersion synergist is smaller than 98% of the molecular weight of the color pigment. Also, methods of preparing the non-aqueous pigment dispersions.

Claims (28)

1. A non-aqueous pigment dispersion comprising:

a color pigment, a polymeric dispersant, and a dispersion synergist in a dispersion medium; wherein

the dispersion synergist is represented by Formula (I):

wherein AR 1 and AR 2 represent a substituted or unsubstituted aromatic group, and R represents a substituted or unsubstituted aliphatic group, with the proviso that one of R, AR 1 , and AR 2 contains at least one carboxylate anion and that the molecular weight of the anionic part of the dispersion synergist is smaller than 98% of the molecular weight of the color pigment.

2. The non-aqueous pigment dispersion according to claim 1 , wherein the dispersion synergist is represented by Formula (II):

wherein one of R1 to R11 represents or contains at least one carboxylate anion and its proton or cation;

R1 to R11, if not representing or containing the at least one carboxylate anion and its proton or cation, are independently selected from the group consisting of hydrogen, an alkyl group, an alkenyl group, an alkoxy group, an alcohol group, an ester group, an acyl group, a nitro group, an amide group, and a halogen; and

R7 and R8 may together form a heterocyclic ring.

3. The non-aqueous pigment dispersion according to claim 2 , wherein the heterocyclic ring formed by R7 and R8 is imidazolone or 2,3-dihydroxypyrazine.

4. The non-aqueous pigment dispersion according to claim 1 , wherein the cationic part of the dispersion synergist consists of one or more protons and/or cations to compensate for the charge of the anionic part of the dispersion synergist.

5. The non-aqueous pigment dispersion according to claim 4 , wherein the cation is selected from the group consisting of Li + , ammonium, and a substituted ammonium group.

6. The non-aqueous pigment dispersion according to claim 5 , wherein the substituted ammonium group is selected from the group consisting of + N(CH 3 ) 2 (C 18 H 37 ) 2 , + NH(CH 3 ) 2 (C 18 H 37 ), + N(CH 3 ) 2 (C 12 H 25 ) 2 , + NH(CH 3 ) 2 (C 12 H 25 ), + N(CH 3 ) 2 (C 10 H 21 ) 2 , + NH(CH 3 ) 2 (C 10 H 21 ), + N(CH 3 ) 2 (C 8 H 17 ) 2 , + NH(CH 3 ) 2 (C 8 H 17 ), + NH(C 8 H 17 ) 3 , + NH(C 10 H 21 ) 3 , + NH(C 12 H 25 ) 3 , and + NH(C 18 H 35 ) 3 .

7. The non-aqueous pigment dispersion according to claim 1 , wherein the dispersion synergist contains an aromatic acid group or a salt thereof.

8. The non-aqueous pigment dispersion according to claim 7 , wherein the aromatic acid group or a salt thereof is a benzoic acid group or a phtalic acid group, or salts thereof.

9. The non-aqueous pigment dispersion according to claim 1 , wherein the color pigment is selected from the group consisting of C.I. Pigment Yellow 120, C.I. Pigment Yellow 155, C.I. Pigment Yellow 180, C.I. Pigment Yellow 194, and C.I. Pigment Yellow 213.

10. The non-aqueous pigment dispersion according to claim 9 , wherein the color pigment is selected from the group consisting of C.I. Pigment Yellow 120, C.I. Pigment Yellow 180, C.I. Pigment Yellow 194, and C.I. Pigment Yellow 213; and

the dispersion synergist is:

wherein R represents hydrogen or methyl.

11. The non-aqueous pigment dispersion according to claim 9 , wherein the color pigment is selected from the group consisting of C.I. Pigment Yellow 120, C.I. Pigment Yellow 155, and C.I. Pigment Yellow 213; and

the dispersion synergist is

wherein R represents hydrogen or methyl.

12. The non-aqueous pigment dispersion according to claim 1 , wherein the pigment dispersion is a curable inkjet ink.

13. The non-aqueous pigment dispersion according to claim 1 , wherein the pigment dispersion is a non-aqueous inkjet ink containing an organic solvent and/or oil.

14. The non-aqueous pigment dispersion according to claim 1 , wherein the dispersion synergist further contains a sulphonic acid or a phosphoric acid group, or salts thereof.

15. A method of preparing the non-aqueous pigment dispersion according to claim 1 , comprising the step of:

adding the dispersion synergist to the color pigment in the dispersion medium.

16. The non-aqueous pigment dispersion according to claim 1 , wherein the pigment dispersion is a UV curable pigment dispersion.

17. The non-aqueous pigment dispersion according to claim 1 , wherein the pigment dispersion is a curable pigmented inkjet ink.

Assignments (2)
CHANGE OF NAME Recorded Jan 3, 2018
From: AGFA GRAPHICS NV
To: AGFA NV
Reel/Frame 045742/0598 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 23, 2008
From: DEROOVER, GEERT; POINT, NICOLAS
To: AGFA GRAPHICS NV
Reel/Frame 020989/0808 →