IP Library Granted Patent US 8,118,924
Granted Patent B2
US 8,118,924 · App. 13/109,865 · Granted Feb 21, 2012

Self-dispersed pigments and methods for making and using the same

Assignee: Sensient Colors LLC
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Quick Facts
Patent No.
US 8,118,924
App. No.
13/109,865
Granted
Feb 21, 2012
Kind
B2
Abstract

A method of modifying a pigment that includes reacting a reactive compound having an X—[Y] n reactive group with a secondary compound N—S—ZM to form a substituted reactive intermediate [Y] a —X—(N—S—ZM) b . A pigment is reacted with the substituted reactive intermediate [Y] a —X—(N—S—ZM) b to attach the substituted reactive intermediate to the surface of the pigment to form a surface modified pigment. X may be a sulfonyl, phosphoryl, or 1,3,5-triazinyl group, Y may be a halogen leaving group, N may be a basic nucleophilic group, S may be an organic group, and ZM may be an ionizable end group. Also, n is an integer between 1 and 3, b is an integer between 1 and 3, and a=n−b. When n is equal to or greater than b, and if b is 2 or 3, each. N—S—ZM can be the same or different.

Claims (11)

1. A method of modifying a pigment, the method comprising:

reacting cyanuric chloride with about three equivalents of a secondary compound or a mixture of secondary compounds to displace all reactive chlorines to form a substituted triazine; and

reacting the substituted triazine with a surface of a pigment to form a surface modified pigment.

2. The method of claim 1 , further comprising reacting the substituted triazine with the surface of the pigment using a radical initiator to form a surface modified pigment.

3. The method of claim 2 , wherein the radical initiator comprises a persulfate.

4. The method of claim 1 , wherein the mixture of secondary compounds may include one, two, or three different secondary compounds.

5. The method of claim 1 , wherein the method is carried out at a temperature of about 25° C. to about 90° C.

6. The method of claim 1 , wherein the secondary compound or mixture of secondary compounds comprises at least one of amino benzoic acids, amino benzene sulfonic acids, amino phenols, amino sulfonic acids, polyethoxylated amino acids, sodium sulfanilate, sulfanilic acid, sodium p-aminobenzoate, p-aminophenol, ethyl 4-aminobenzoate, tetramethylammonium 4-aminobenxoate, sodium 4-aminophenolate, taurine, oleic acid (amino), sodium aminooleate, organic polymeric substrates, linear polyethoxy polymeric amines, linear propoxy polymeric amines, a diamino aromatic, a polyethyleneimine, a polyguanidine, a quarternary ammonium compound, or a combination thereof.

7. The method of claim 1 , wherein the pigment comprises at least one of carbon black, pigment red 122, pigment violet 19, pigment violet 23, pigment red 202, pigment red 188, pigment yellow 155, pigment yellow 97, pigment green 7, pigment blue 15:3, pigment blue 15:4, and pigment yellow 74, and combinations thereof.

8. The method of claim 1 , further comprising milling the pigment to less than about 100 nm before, during, or after reacting the pigment with the substituted triazine.

9. The method of claim 1 , wherein the surface modified pigment comprises about 0.01 to about 1.0 mMoles of S and about 0.01 to about 2.0 mMoles of active hydrogen per gram of pigment.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2012
From: SUJEETH, PUTHALATH K.; KANE, JOHN P.; OUELLETTE, DANIEL A.; ULRICH, MARK; SHING, VINCENT; BOGOMOLNY, MICHAEL
To: SENSIENT COLORS INC.
Reel/Frame 027545/0815 →
MERGER Recorded Jan 17, 2012
From: SENSIENT COLORS INC.
To: SENSIENT COLORS LLC
Reel/Frame 027545/0867 →
Continuity (3)
Division 12197087 · Aug 22, 2008
Provisional Application 60957596 · Aug 23, 2007
Related Publication 20110308430A1 · Dec 22, 2011