Quinacridone nanoscale pigment particles and methods of making same
View Patent ↗A process for preparing coated nanoscale quinacridone pigment particles, includes: mixing a quinacridone pigment precursor or crude quinacridone pigment with a first solution including an acid to form nanoscale quinacridone pigment particles; adding the first solution and formed nanoscale quinacridone pigment particles into a second solution including deionized water to form a third solution and to precipitate the nanoscale quinacridone pigment particles; and washing the precipitated nanoscale quinacridone pigment particles in a fourth solution including a surface additive compound, whereby the surface additive compound coats the nanoscale quinacridone pigment particles; wherein the surface additive compound is a rosin compound.
1. A process for preparing coated nanoscale quinacridone pigment particles, comprising:
mixing a quinacridone pigment precursor or crude quinacridone pigment with a first solution comprising an acid to form nanoscale quinacridone pigment particles;
adding the first solution and formed nanoscale quinacridone pigment particles into a second solution comprising deionized water to form a third solution and to precipitate the nanoscale quinacridone pigment particles; and
washing the precipitated nanoscale quinacridone pigment particles in a fourth solution comprising a surface additive compound, whereby said surface additive compound coats the nanoscale quinacridone pigment particles;
wherein the surface additive compound comprises a rosin compound.
2. The process of claim 1 , further comprising heating the quinacridone pigment precursor or crude quinacridone pigment in said first solution.
3. The process of claim 1 , further comprising neutralizing the third solution by adding a neutralizing agent.
4. The process of claim 3 , wherein the neutralizing agent is selected from the group consisting of an ammonia solution, alkali metal hydroxides, and alkali metal carbonates.
5. The process of claim 1 , wherein the coated nanoscale quinacridone pigment particles have an average particle diameter of less than about 150 nm as derived from Transmission Electron Microscopy.
6. The process of claim 1 , wherein the nanoscale quinacridone pigment particles are formed from a quinacridone precursor selected from the group consisting of 2,5-dianilino terephthalic acid derivatives, compounds of Formula 1 and esters and amides thereof that possess linear, branched or cyclic alkyl groups having from 1 to about 20 carbon atoms
wherein R represents hydrogen, a linear, branched or cyclic alkyl group having from 1 to about 20 carbon atoms, or substituted or unsubstituted aryl groups; R 1 and R 2 each independently represents H, alkyl, alkoxyl, and aryloxyl groups, and halogen atoms.
7. The process of claim 1 , wherein the nanoscale quinacridone pigment particles are formed from a quinacridone precursor selected from the group consisting of compounds of the following Formula (1):
wherein R represents hydrogen, a linear, branched or cyclic alkyl group having from 1 to about 20 carbon atoms, or substituted or unsubstituted aryl groups; R 1 and R 2 each independently represents H, alkyl, alkoxyl, and aryloxyl groups, and halogen atoms.
8. The process of claim 7 , wherein the nanoscale quinacridone pigment particles are formed from a quinacridone precursor selected from the group consisting of:
a) compound of the formula (1) wherein R 1 ═R 2 ═H;
b) compound of the formula (1) wherein R 1 ═H, R 2 =halide;
c) compound of the formula (1) wherein R 1 ═R 2 ═CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 , CH(CH 3 ) 2 ;
d) compound of the formula (1) wherein R 1 ═H, R 2 ═CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 , CH(CH 3 ) 2 ;
e) compound of the formula (1) wherein R 1 ═CH 3 , CH 2 CH 3 , CH 2 CH 2 CH 3 , CH(CH 3 ) 2 ; R 2 =halide;
f) compound of the formula (1) wherein R 1 ═R 2 =halide;
g) compound of the formula (1) wherein R 1 ═C 1 , R 2 ═Br;
h) compound of the formula (1) wherein R 1 ═R 2 ═OCH 3 , O—CH 2 CH 3 , O—CH 2 CH 2 CH 3 , O—CH(CH 3 ) 2 , O—(CH 2 )C 6 H 5 ;
i) compound of the formula (1) wherein R 1 ═H, R 2 ═OCH 3 , O—CH 2 CH 3 , O—CH 2 CH 2 CH 3 , O—CH(CH 3 ) 2 , O—(CH 2 )C 6 H 5 and
j) compound of the formula (1) wherein R 1 ═OCH 3 , O—CH 2 CH 3 , O—CH 2 CH 2 CH 3 , O—CH(CH 3 ) 2 , O—(CH 2 )C 6 H 5 , R 2 =halide.
9. The process of claim 1 , wherein the fourth solution comprises a solvent and the surface additive compound.
10. The process of claim 9 , wherein the solvent is selected from the group consisting of deionized water, acetone, ketones, toluene, and mixtures thereof.
11. The process of claim 1 , wherein the rosin compound is selected from the group consisting of hydrogenated and non-hydrogenated forms of rosin, rosin esters, rosin acids, rosin salts, and mixtures thereof.
12. The process of claim 1 , wherein the rosin compound is selected from the group consisting of hydrogenated rosin glycerin ester, levopimaric acid, neoabietic acid, palustric acid, abietic acid, dehydroabietic acid, seco-dehydroabietic acid, tetrahydroabietic acid, dihydroabietic acid, pimaric acid, and isopimaric acid, calcium resonates, zinc resonates, magnesium resonates, barium resonates, lead resonates, cobalt resonates, mixed resonates, sodium salts of rosins, alkyl esters of rosin or hydrogenated rosin, and mixtures thereof.
13. The process of claim 1 , wherein the surface additive compound forms a continuous or substantially continuous coating on said nanoscale quinacridone pigment particles.
14. The process of claim 1 , wherein the surface additive compound improves dispersibility and stability of the nanoscale quinacridone pigment particles in an ink vehicle.
15. The process of claim 1 , comprising adding crude quinacridone pigment to said first solution.
16. The process of claim 1 , wherein the acid is selected from the group consisting of strong mineral acids and strong organic acids.
17. The process of claim 15 , wherein the acid is selected from the group consisting of sulfuric acid, nitric acid, perchloric acid, hydrohalic acids, fluorosulfonic acid, chlorosulfonic acid, phosphoric acid and polyphosphoric acid, boric acid, organo-sulfonic acids, arenesulfonic acids, acetic acid, haloacetic, dihaloacetic, trihaloacetic acids, cyanoacetic acid, and mixtures thereof.
18. The process of claim 1 , further comprising adding a precipitating agent to at least one of the second and third solutions.
19. The process of claim 1 , wherein the precipitating is conducted at a temperature of from about 0 to about 90° C.
20. The process of claim 1 , comprising adding quinacridone pigment precursor to said first solution.
21. The process of claim 20 , wherein the adding quinacridone pigment precursor to said first solution further comprises a chemical transformation to form quinacridone pigment molecules from said quinacridone pigment precursor.
22. The process of claim 1 , wherein a concentration of the coated nanoscale quinacridone pigment particles present in the third solution is from about 0.5% to about 20% by weight.