Pigment compositions and processes therefor

• US 4,444,592 A
• Filed: 11/15/1982
• Issued: 04/24/1984
• Est. Priority Date: 06/02/1981
• Status: Expired due to Fees

• Current Assignee: PMC Incorporated (PMC Global Incorporated)
• Original Assignee: Sherwin-Williams Company
• Inventors: Ludwig, Thomas E.
• Primary Examiner(s): Kight, III, John
• Assistant Examiner(s): YARBROUGH, AMELIA
• Application Number:
  US06/441,840
• Time in Patent Office: 526 Days
• Field of Search: 106/22, 106/288 Q, 106/289, 106/23, 106/309
• US Class Current: 106/413
• CPC Class Codes: C09B 69/06 of cationic dyes with organic acids or with inorganic complex acids
• CPC Class Codes: C09D 11/037 characterised by the pigment

Abstract

This invention relates to novel pigmentary products, particularly valuable in the textile art, prepared by using strong acid solvents to solubilize or form fine colloidal dispersions of normally water-insoluble aryl pararosanilines in an aqueous medium. The aryl pararosaniline which is thus solubilized or dispersed is reacted with a heteropoly acid to produce water-insoluble blue-hued pigments. By various modifications in the process, the pigments can be co-precipitated with other pigments and/or dyes to produce pigments or pigment lakes of different shades and intensities.

Claims

1. Blue pigments which comprise the reaction product obtained by dissolving and/or dispersing an essentially water-insoluble aryl pararosaniline in an effective amount of at least one acid solvent and reacting with an approximately chemically equivalent amount of at least one heteropoly acid containing molybdenum and/or tungsten;

wherein said aryl pararosaniline has the following structure in its carbinol form;

##STR3## wherein R₁, R₂ and R₃ are direct linkages, phenyl, or napthyl groups;

R₄ is hydrogen or methyl;

X₁, X₂ and X₃ are hydrogen, halogen, nitro, alkyl of 1 to 4 carbons or alkoxy of 1 to 4 carbons;

provided that at least one of R₁, R₂ and R₃ is not a direct linkage and provided that X₁, X₂ or X₃ is hydrogen when the corresponding R₁, R₂ or R₃ is a direct linkage.

2. The pigments of claim 1 further characterized in that the heteropoly acid is at least one acid selected from the group consisting of phosphotungstic acid, silicotungstic acid, cobaltotungstic acid, vanadotungstic acid, aluminotungstic acid, manganotungstic acid, chromotungstic acid, nickelotungstic acid and ferrotungstic acid.

3. The pigments of claim 1 further characterized in that the heteropoly acid is selected from the group consisting of phosphomolybdic acid, silicomolybdic acid, cobaltomolybdic acid, vanadomolybdic acid, aluminomolybdic acid, manganomolybdic acid, chromomolybdic acid, nickelomolybdic acid and ferromolybdic acid.

4. The pigments of claim 1 further characterized in that at least one basic dye is present during the reaction in an amount ranging up to about 50% by weight of the aryl pararosaniline.

5. The pigments of claim 4 wherein the basic dye is selected from the group of basic dyes consisting of the diphenyl methane, xanthene, acridine, methine, azine and induline dyes.

6. The pigments of claim 1 further characterized in that at least one chromatic pigment or dye is present in amounts ranging up to about 50% by weight of the aryl pararosaniline.

7. The pigments of claim 6 wherein the chromatic pigment or dye is selected from the group of dyes and pigments consisting of azo, phthalocyanine, carbazole, quinacridone and indigoid.

8. The pigments of claim 1 further characterized in that at least one chromatic pigment or dye is present in an amount ranging up to about 50% by weight of the aryl pararosaniline and at least one basic dye is also present in an amount ranging up to about 50% by weight of the aryl pararosanilines.

9. The pigments of claim 8 further characterized in that the basic dye is methyl violet and the chromatic pigment is copper phthalocyanine.

10. The pigments of claim 1 further characterized in that a black pigment or dye is also present in an amount ranging up to about 50% by weight of the aryl pararosaniline.

11. A laked pigment which comprises the reaction product obtained by dissolving and/or dispersing an essentially water-insoluble aryl pararosaniline in an effective amount of at least one acid solvent and reacting the aryl pararosaniline with an approximately chemically equivalent amount of at least one heteropoly acid containing molybdenum and/or tungsten;

wherein said reaction takes place in the presence of a finely dispersed suspended inert pigment; and

wherein said aryl pararosaniline has the following structure in its carbinol form;

##STR4## wherein R₁, R₂ and R₃ are direct linkages, phenyl, or napthyl groups;

R₄ is hydrogen or methyl;

X₁, X₂ and X₃ are hydrogen, halogen, nitro, alkyl of 1 to 4 carbons or alkoxy of 1 to 4 carbons;

provided that at least one of R₁, R₂ and R₃ is not a direct linkage and provided that X₁, X₂ or X₃ is hydrogen when the corresponding R₁, R₂ or R₃ is a direct linkage.

12. The pigments of claim 11 further characterized in that the inert pigment is selected from the group consisting of china clay, kaolin, talc, fullers earth, bentonite, silica, sodium aluminosilicate, blanc fixe, wollastinite, nephaline syenite, and mica.

13. A process for producing blue pigments which comprises dissolving and/or dispersing an essentially water-insoluble aryl pararosaniline in an effective amount of at least one acid solvent and reacting the aryl pararosaniline with an approximately chemically equivalent amount of at least one heteropoly acid containing molybdenum and/or tungsten;

wherein said aryl pararosaniline has the following structure in its carbinol form;

##STR5## wherein R₁, R₂ and R₃ are direct linkages, phenyl, or napthyl groups;

R₄ is hydrogen or methyl;

X₁, X₂ and X₃ are hydrogen, halogen, nitro, alkyl of 1 to 4 carbons or alkoxy of 1 to 4 carbons;

provided that at least one of R₁, R₂ and R₃ is not a direct linkage and provided that X₁, X₂ or X₃ is hydrogen when the corresponding R₁, R₂ or R₃ is a direct linkage.

14. The process of claim 13 further characterized in that the acid solvent has a pKa less than about 3.0.

15. The process of claim 13 further characterized in that the acid solvent is selected from the group consisting of organic sulfonic acids, sulfuric acid, phosphoric acid, and blends thereof.

16. The process of claim 13 further characterized in that the acid solvent is present in an amount ranging from about 1 to about 40 times the weight of the aryl pararosaniline.

17. The process of claim 13 further characterized in that the solvent is a blend of sulfuric acid and phosphoric acid.

18. The process of claim 17 further characterized in that the sulfuric acid comprises 20% to 95% by weight of the solvent combination.

19. The process of claim 18 further characterized in that water is present in an amount ranging from at least about 10% by weight of the acid solvent.

20. The process of claim 19 further characterized in that an effective amount of a surfactant is also present.

21. The process of claim 13 further characterized in that the acid solvent comprises a mixture of at least one sulfonic acid, sulfuric acid, and phosphoric acid.

22. The process of claim 21 further characterized in that water is present in an amount ranging from at least about 10% by weight of the acid solvent.

23. A process for preparing pigments which comprise admixing at an effective temperature:

(a) an aqueous heteropoly acid containing molybdenum and/or tungsten;

(b) a dispersion or solution which comprises;

(i) about 1 to about 40 parts of an acid solvent;

(ii) about 0 to 100 parts water;

(iii) about 1 part of a reactant mixture which comprises

(I) about 50 to 100% of an aryl pararosaniline having the following structure in its carbinol form;

##STR6## wherein R₁, R₂ and R₃ are direct linkages, phenyl, or napthyl groups;

R₄ is hydrogen or methyl;

X₁, X₂ and X₃ are hydrogen, halogen, nitro, alkyl of 1 to 4 carbons or alkoxy of 1 to 4 carbons;

provided that at least one of R₁, R₂ and R₃ is not a direct linkage and provided that X₁, X₂ or X₃ is hydrogen when the corresponding R₁, R₂ or R₃ is a direct linkage;

(II) about 0 to 50% of a basic dye;

(III) about 0 to 50% of a black or chromatic dye or pigment;

(iv) about 0 to 1 part surfactant;

wherein the heteropoly acid is present at an approximately chemically equivalent amount to the total equivalents of aryl pararosaniline and basic dye.

24. A process for the production of laked pigments which comprises dissolving or dispersing an essentially water-insoluble aryl pararosaniline in an effective amount of at least one acid solvent and reacting the aryl pararosaniline with an approximately chemically equivalent amount of at least one heteropoly acid containing molybdenum and/or tungsten;

wherein said reaction takes place in the presence of a finely dispersed suspended inert pigment; and

wherein said aryl pararosaniline has the following structure in its carbinol form;

##STR7## wherein R₁, R₂ and R₃ are direct linkages, phenyl, or napthyl groups;

R₄ is hydrogen or methyl;

X₁, X₂ and X₃ are hydrogen, halogen, nitro, alkyl or 1 to 4 carbons or alkoxy of 1 to 4 carbons;

provided that at least one of R₁, R₂ and R₃ is not a direct linkage and provided that X₁, X₂ or X₃ is hydrogen when the corresponding R₁, R₂ or R₃ is a direct linkage.

25. The process of claim 24 further characterized in that the inert pigment is present at a level of about 0.25 to 2.0 parts inert to each part of the pigment formed by the reaction of the heteropoly acid and the aryl pararosaniline.