IP Library Granted Patent US 7,077,898
Granted Patent B2
US 7,077,898 · App. 10/886,487 · Granted Jul 18, 2006

Black pigment compositions

Assignee: Ciba Specialty Chemicals Corporation
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Quick Facts
Patent No.
US 7,077,898
App. No.
10/886,487
Granted
Jul 18, 2006
Kind
B2
Abstract

The present invention relates to black pigment compositions comprising (a) carbon black, and (b) a compound of the formula (MO 3 S) m -Q (CH 2 ) k —X] n ,  (I) wherein Q is a pigment or pigment intermediate radical selected from the group of anthraquinone, perinone, perylene, diketopyrrolopyrrole, thioindigo, iminoisoindoline, iminoisoindolinone, quinacridone, 6,13-dihydroquinacridone, flavanthrone, dioxazine, indanthrone, anthrapyrimidine and quinophthalone, X is a cyclo hetero aliphatic group with at least one 5 or 6 atom ring or a hetero aromatic group with at least one 6 atom ring, M is hydrogen, a metal cation or nitrogen cation, k is 0 or 1, and m and n are each independently of the other from 0 to 4, wherein 0 and 4 are not simultaneously 0. Compositions are useful for coloring high molecular weight material, like inks, plastics and in particular automotive coatings.

Claims (71)

1. A black pigment composition comprising

(a) carbon black, and

(b) a compound of the formula

(MO 3 S) m —Q (CH 2 ) k —X] n   (I),

wherein

Q is a pigment or pigment intermediate radical selected from the group consisting of anthraquinone, perinone, perylene, diketopyrrolopyrrole, thioindigo, iminoisoindoline, iminoisoindolinone, quinacridone, 6,13-dihydroquinacridone, flavanthrone, dioxazine, indanthrone, anthrapyrimidine and quinophthalone,

X is a cyclohetero aliphatic group or a hetero aromatic group with at least one 5 or 6 atom ring,

M is hydrogen, a metal cation or nitrogen cation,

k is 0 or 1, and

m and n are each independently of the other from 0 to 4, wherein m and n are not simultaneously zero.

2. A black pigment composition according to claim 1 , wherein

the carbon black is selected from the group consisting of C.I. Pigment Black 6, C.I. Pigment Black 9 and C.I. Pigment Black 7.

3. A black pigment composition according to claim 1 , wherein

the carbon black is C.I. Pigment Black 7.

4. A black pigment composition according to claim 1 , wherein

the carbon black has a specific surface area of at least 50 m 2 /g.

5. A black pigment composition according to claim 1 , wherein

the carbon black has a specific surface area of from 100 to 600 m 2 /g.

6. A black pigment composition according to claim 1 , wherein

the carbon black has a specific surface area of from 150 to 600 m 2 /g.

7. A black pigment composition according to claim 1 , wherein

Q is a pigment or pigment intermediate radical selected from the group consisting of 6,13-dihydroquinacridone, quinacridone and indanthrone.

8. A black pigment composition according to claim 1 , wherein

Q is a pigment or pigment intermediate radical selected from the group consisting of 6,13-dihydroquinacridone and quinacridone.

9. A black pigment composition according to claim 1 , wherein

X is a radical selected from the group consisting of imidazolyl, 3,5-dimethylpyrazol-1-yl-, phthalimido and benzosulfimido.

10. A black pigment composition according to claim 1 , wherein

M is hydrogen, a mono-, di- or trivalent metal cation or nitrogen cation.

11. A black pigment composition according to claim 1 , wherein

M is hydrogen, an alkali metal, an alkaline earth metal, or a zinc or aluminum cation.

12. A black pigment composition according to claim 1 , wherein

k is the number 1.

13. A black pigment composition according to claim 1 , wherein

the sum of m and n is from 0.2 to 4.

14. A black pigment composition according to claim 1 , wherein

component (b) is a compound of the formula

Q (CH 2 ) k —X] n   (Ia),

wherein

Q is a pigment or pigment intermediate radical selected from the group consisting of quinacridone and 6,13-dihydroquinacridone,

X is a radical selected from the group of imidazolyl, 3,5-dimethylpyrazol-1-yl-, phthalimido and benzo sulfimido,

k is 1, and

n is from 0.5 to 4.

15. A black pigment composition according to claim 1 , wherein

component (b) is a compound of the formula

Q-(SO 3 M) m   (Ib),

wherein

Q is a pigment or pigment intermediate radical selected from the group consisting of quinacridone and indanthrone,

M is a mono-, di- or trivalent metal cation or ammonium cation, and

m is from 0.5 to 2.

16. A black pigment composition according to claim 1 , comprising

from 50 to 95% by weight of carbon black and from 5 to 50% by weight of the compound of formula (I), based on the total weight of carbon black and the compound of formula (I).

17. A black pigment composition according to claim 16 , comprising

from 70 to 90% by weight of carbon black and from 10 to 30% by weight of the compound of formula (I), based on the total weight of carbon black and the compound of formula (I).

18. A black pigment composition according to claim 16 , comprising

from 75 to 85% by weight of carbon black and from 15 to 25% by weight of the compound of formula (I), based on the total weight of carbon black and the compound of formula (I).

19. A black pigment composition according to claim 1 , wherein

the compound of formula (I) contains 0.05 to 20% by weight of a texture-improving agent, based on the weight of the compound of formula (I).

20. A black pigment composition according to claim 19 , wherein

the texture-improving agent is at least one compound selected from the group consisting of fatty acids having at least 12 carbon atoms, fatty acid amides having at least 12 carbon atoms, fatty acid esters having at least 12 carbon atoms, salts of a fatty acid having at least 12 carbon atoms and fatty amines having at least 12 carbon atoms, fatty alcohols having at least 12 carbon atoms, ethoxylated fatty alcohols having at least 12 carbon atoms, polyols, glycerol mono stearates, polyvinylalcohols, polyvinylpyrrolidones, epoxidized soy bean oils, waxes, resin acids and resin acid salts.

21. A process for the preparation of a black pigment composition according to claim 1 comprising

blending carbon black in a granulated or powdery form with a powder form of the compound of the formula (I) until a uniform blend is generated.

22. A process for coloring a solid or liquid material, comprising

incorporating into said material an effective pigmenting amount of a black pigment composition according to claim 1 .

23. A process according to claim 22 , wherein

the material is selected from the group consisting of a cellulose ether, cellulose ester, natural resin, synthetic polymer, rubber, casein, silicone or silicone resin and mixtures thereof.

24. A process according to claim 22 , wherein

the material is an industrial paint, automotive paint, ink, powder coating, UV/EB cured coating or ink.

25. A process according to claim 22 , wherein

the material is paper, security paper, leather, solid or liquid polymeric material, mineral oil, inorganic material, cosmetic material or seed.

26. A process for coloring a material, comprising

applying to said material a coating composition containing an effective pigmenting amount of a black pigment composition according to claim 1 .

Assignments (12)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2023
From: H.I.G. COLORS HOLDINGS, INC.; H.I.G. COLORS, INC.; DCL HOLDINGS (USA), INC.; DCL CORPORATION (USA), LLC; DCL CORPORATION (BP), LLC; DOMINION COLOUR CORPORATION (USA); DCL CORPORATION
To: PIGMENTS SERVICES, INC.
Reel/Frame 063629/0788 →
RELEASE OF SECURITY INTEREST Recorded May 11, 2023
From: DELAWARE TRUST COMPANY (AS SUCCESSOR IN INTERESTS TO VIRTUS GROUP LP)
To: DCL CORPORATION (F/K/A DOMINION COLOUR CORPORATION)
Reel/Frame 063618/0357 →
SECURITY INTEREST Recorded May 11, 2023
From: PIGMENTS SERVICES, INC.
To: DELAWARE TRUST COMPANY
Reel/Frame 063618/0459 →
RELEASE OF SECURITY INTEREST Recorded May 2, 2023
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: DCL CORPORATION (F/K/A DOMINION COLOUR CORPORATION)
Reel/Frame 063512/0678 →
SECURITY AGREEMENT Recorded Apr 17, 2023
From: PIGMENTS SERVICES, INC.
To: WELLS FARGO BANK, N.A.
Reel/Frame 063350/0453 →
AGREEMENT OF AGENT RESIGNATION, APPOINTMENT AND ACCEPTANCE Recorded Jul 1, 2022
From: VIRTUS GROUP, LP
To: DELAWARE TRUST COMPANY
Reel/Frame 060952/0618 →
SECURITY AGREEMENT Recorded Apr 26, 2018
From: DOMINION COLOUR CORPORATION
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 046022/0547 →
SECURITY AGREEMENT Recorded Apr 26, 2018
From: DOMINION COLOUR CORPORATION
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 046024/0375 →
PATENT SECURITY AGREEMENT Recorded Apr 10, 2018
From: DOMINION COLOUR CORPORATION
To: VIRTUS GROUP, LP
Reel/Frame 045889/0272 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2010
From: CIBA CORP.
To: DOMINION COLOUR CORPORATION
Reel/Frame 023905/0241 →
CHANGE OF NAME Recorded Feb 5, 2010
From: CIBA SPECIALTY CHEMICALS CORPORATION
To: CIBA CORP.
Reel/Frame 023905/0624 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2004
From: BABLER, FRIDOLIN
To: CIBA SPECIALTY CHEMICALS CORP.
Reel/Frame 015857/0928 →
Continuity (2)
Provisional Application 6048815600 · Jul 17, 2003
Related Publication 20050014863A1 · Jan 20, 2005