IP Library Granted Patent US 8,226,761
Granted Patent B2
US 8,226,761 · App. 13/355,131 · Granted Jul 24, 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 8,226,761
App. No.
13/355,131
Granted
Jul 24, 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 (19)

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

attaching a reactive group X—Y to a surface of a pigment; and

subsequently displacing Y with an organic substrate N—S—ZM to form a surface-modified pigment having attached X—N—S—ZM;

wherein X is a sulfonyl, phosphoryl, or 1,3,5-triazine group;

Y is fluorine, chlorine, bromine, or iodine;

N is an amine, an imine, a pyridine, or a thiol group;

S is substituted or unsubstituted alkyls, aryls, or polymer chains having a molecular weight range from about 300 to about 8000;

Z is a carboxyl, sulfonyl, phenolic, phosphoryl, ammonium, trimethylammonium, or tributylammonium group; and

M is a halide, a negatively charged ion, a proton in salt form, or a cation in salt form.

2. The method of claim 1 , wherein X is a sulfonyl group.

3. The method of claim 2 , wherein the reactive group X—Y is attached to the surface of the pigment by chlorosulfonation with a chlorosulfonating agent comprising chlorosulfonic acid, thionyl chloride, or a combination thereof.

4. The method of claim 3 , wherein the ratio of pigment to chlorosulfonating agent is at least about 4:1 (wt/wt).

5. The method of claim 3 , wherein the ratio of pigment to chlorosulfonating agent is from about 1:20 to about 1:1 (wt/wt).

6. The method of claim 3 , wherein the chlorosulfonating agent is a mixture of chlorosulfonic acid and thionyl chloride in a ratio of about 3:1 to about 6:1 (wt/wt).

7. The method of claim 3 , wherein the chlorosulfonation is carried out at a temperature of about 25° C. to about 160° C.

8. The method of claim 2 , further comprising:

modifying a majority of the pigment surface to form a liquid gel; and

subsequently milling the liquid gel with excess untreated pigment and water to form a stable aqueous pigment dispersion.

9. The method of claim 8 , wherein the modifying the majority of the pigment surface comprises chlorosulfonating a pigment at a temperature of at least about 90° C. for at least about one hour to form a pigment sulfonyl chloride.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 23, 2012
From: SUJEETH, PUTHALATH K.; KANE, JOHN P.; OUELLETTE, DANIEL A.; ULRICH, MARK; SHING, VINCENT; BOGOMOLNY, MICHAEL
To: SENSIENT COLORS INC.
Reel/Frame 027578/0320 →
MERGER Recorded Jan 23, 2012
From: SENSIENT COLORS INC.
To: SENSIENT COLORS LLC
Reel/Frame 027578/0410 →
Continuity (4)
Division 13109865 · May 17, 2011
Division 12197087 · Aug 22, 2008
Provisional Application 60957596 · Aug 23, 2007
Related Publication 20120118205A1 · May 17, 2012