Nanosized particles of monoazo laked pigment
View Patent ↗A nanoscale pigment particle composition includes an organic monoazo laked pigment including at least one functional moiety, and a sterically bulky stabilizer compound including at least one functional group, wherein the functional moiety associates non-covalently with the functional group; and the presence of the associated stabilizer limits the extent of particle growth and aggregation, to afford nanoscale-sized pigment particles.
1. A nanoscale pigment particle composition, comprising:
an organic monoazo laked pigment having at least one functional moiety, and
a sterically bulky stabilizer compound having at least one functional group,
wherein the functional moiety associates non-covalently with the functional group; and
presence of the associated stabilizer limits an extent of particle growth and aggregation, to afford nanoscale-sized pigment particles.
2. The composition of claim 1 , wherein the nanoscale-sized pigment particles have an average particle diameter as derived from transmission electron microscopy imaging, of less than about 150 nm.
3. The composition of claim 1 , wherein the at least one functional moiety of the organic monoazo laked pigment is selected from the group consisting of sulfonate/sulfonic acid, (thio)carboxylate/(thio)carboxylic acid, phosphonate/phosphonic acid, ammonium and substituted ammonium salts, phosphonium and substituted phosphonium salts, substituted carbonium salts, substituted arylium salts, alkyl/aryl (thio)carboxylate esters, thiol esters, primary or secondary amides, primary or secondary amines, hydroxyl, ketone, aldehyde, oxime, hydroxylamino, enamines (or Schiff base), porphyrins, (phthalo)cyanines, urethane or carbamate, substituted ureas, guanidines and guanidinium salts, pyridine and pyridinium salts, imidazolium and (benz)imidazolium salts, (benz)imidazolones, pyrrolo, pyrimidine and pyrimidinium salts, pyridinone, piperidine and piperidinium salts, piperazine and piperazinium salts, triazolo, tetraazolo, oxazole, oxazolines and oxazolinium salts, indoles, and indenones.
4. The composition of claim 1 , wherein the organic monoazo laked pigment comprises a diazonium component linked to a coupling component through an azo or hydrazone group, with a counterion.
5. The composition of claim 4 , wherein the coupling component is selected from the group consisting of β-naphthol and derivatives thereof, naphthalene sulfonic acid derivatives, pyrazolone derivatives, and acetoacetic arylide derivatives.
6. The composition of claim 4 , wherein the counterion is selected from the group consisting of metals, non-metals, and carbon-based cations or anions.
7. The composition of claim 1 , wherein the at least one functional group of the sterically bulky stabilizer is selected from the group consisting of sulfonate/sulfonic acid, (thio)carboxylate/(thio)carboxylic acid, phosphonate/phosphonic acid, ammonium and substituted ammonium salts, phosphonium and substituted phosphonium salts, substituted carbonium salts, substituted arylium salts, alkyl/aryl (thio)carboxylate esters, thiol esters, primary or secondary amides, primary or secondary amines, hydroxyl, ketone, aldehyde, oxime, hydroxylamino, enamines (or Schiff base), porphyrins, (phthalo)cyanines, urethane or carbamate, substituted ureas, guanidines and guanidinium salts, pyridine and pyridinium salts, imidazolium and (benz)imidazolium salts, (benz)imidazolones, pyrrolo, pyrimidine and pyrimidinium salts, pyridinone, piperidine and piperidinium salts, piperazine and piperazinium salts, triazolo, tetraazolo, oxazole, oxazolines and oxazolinium salts, indoles, and indenones.
8. The composition of claim 1 , wherein the sterically bulky stabilizer comprises at least one aliphatic hydrocarbon moiety.
9. The composition of claim 1 , further comprising a surfactant selected from the group consisting of derivatives of rosin natural products; acrylic-based polymers; styrene-based copolymers; copolymers of α-olefins; copolymers of vinyl pyridine, vinyl imidazole, and vinyl pyrrolidinone; polyester copolymers; polyamide copolymers; and copolymers of acetals and acetates.
10. The composition of claim 1 , wherein the non-covalent association between the organic monoazo laked pigment and the sterically bulky stabilizer compound is at least one of van der Waals' forces, ionic bonding, coordination bonding, hydrogen bonding, and aromatic pi-stacking bonding.
11. The composition of claim 1 , wherein the nanoscale-sized monoazo laked pigment composition has coloristic properties that are changeable as a function of particle size of the nanoscale-sized articles.
12. The composition of claim 11 wherein the coloristic properties are selected from L*, a*, b*, hue, chroma, and NLSI value.
13. The composition of claim 1 , wherein the nanoscale-sized monoazo laked pigment composition has enhanced chroma as compared to a similar organic monoazo laked pigment not having the sterically bulky stabilizer compound and not being of nanoscale-size.
14. The composition of claim 1 , wherein when the nanoscale pigment particle composition is dispersed in a poly(vinyl butyral-co-vinyl alcohol-co-vinyl acetate) polymer binder, a coating formed from the dispersion has a hue angle measured within a range spanning from about 345° to about 0° on a 2-dimensional b* a* magenta color gamut space.
15. The composition of claim 1 , wherein when the nanoscale pigment particle composition is dispersed in a poly(vinyl butyral-co-vinyl alcohol-co-vinyl acetate) polymer binder, the pigment exhibits a NLSI value of from about 0.01 to about 3.
16. The composition of claim 1 , wherein the sterically bulky stabilizer is selected from the group consisting of the following compounds:
wherein Z is H, a metal cation, or an organic cation;
wherein Z is H, a metal cation, or an organic cation, and m+n>1;
wherein Z is H, a metal cation, or an organic cation, and m+n>1 per branch;
wherein Z is H, a metal cation, or an organic cation, and m≧1;
wherein Z is H, a metal cation, or an organic cation, and m≧1; and
wherein Z is H, a metal cation, or an organic cation, and n≧1.
17. The composition of claim 4 , wherein the diazo component is a compound of Formula (2):
where R 1 , R 2 , and R 3 independently represent H, a straight or branched alkyl group of from about 1 to about 10 carbon atoms, halogen, NH 2 , NO 2 , CO 2 H, or CH 2 CH 3 ; and FM represents SO 3 H, —C(═O)—NH-Aryl-SO 3 − (where the aryl group can be unsubstituted or substituted with either halogens or alkyl groups having from about 1 to about 10 carbons), CO 2 H, halogen, NH 2 , or —C(═O)—NH 2 ,
or is a compound of Formula (3):
18. The composition of claim 17 , wherein the diazo component is selected from the group consisting of the following compounds of Formula (2) wherein:
FM is SO 3 H, R 1 is CH 3 , R 2 is H, and R 3 is NH 2 ,
FM is SO 3 H, R 1 is CH 3 , R 2 is Cl, and R 3 is NH 2 ,
FM is SO 3 H, R 1 is Cl, R 2 is CH 3 , and R 3 is NH 2 ,
FM is SO 3 H, R 1 is Cl, R 2 is CO 2 H, and R 3 is NH 2 ,
FM is SO 3 H, R 1 is Cl, R 2 is CH 2 CH 3 , and R 3 is NH 2 ,
FM is SO 3 H, R 1 is Cl, R 2 is Cl, and R 3 is NH 2 ,
FM is SO 3 H, R 1 is H, R 2 is NH 2 , and R 3 is H,
FM is SO 3 H, R 1 is H, R 2 is NH 2 , and R 3 is CH 3 ,
FM is SO 3 H, R 1 is NH 2 , R 2 is H, and R 3 is Cl,
FM is SO 3 H, R 1 is H, R 2 is H, and R 3 is NH 2 ,
FM is SO 3 H, R 1 is H, R 2 is NH 2 , and R 3 is H,
FM is SO 3 H, R 1 is NO 2 , R 2 is NH 2 , and R 3 is H,
FM is —C(═O)—NH-Phenyl-SO 3 − , R 1 is NH 2 , R 2 is CH 3 , and R 3 is H,
FM is CO 2 H, R 1 is H, R 2 is H, and R 3 is NH 2 ,
FM is Cl, R 1 is H, R 2 is H, and R 3 is NH 2 ,
FM is NH 2 , R 1 is CH 3 , R 2 is H, and R 3 is H,
FM is NH 2 , R 1 is H, R 2 is CH 3 , and R 3 is H,
FM is —C(═O)NH 2 , R 1 is NH 2 , R 2 is CH 3 , and R 3 is H,
FM is —C(═O)NH 2 , R 1 is H, R 2 is NH 2 , and R 3 is H, and
FM is NH 2 , R 1 is H, R 2 is H, and R 3 is H.
19. The composition of claim 4 , wherein the coupling component is selected from the group consisting of compounds of Formulas (4)-(8), wherein * denotes a point of coupling or attachment to the azo or hydrazone group:
where FM represents H, CO 2 H, SO 3 H, —C(═O)—NH-Aryl-SO 3 − where the aryl group can be unsubstituted or substituted with either halogens, or alkyl groups having from about 1 to about 10 carbons, CO 2 H, halogen, NH 2 , —C(═O)—NH 2 , substituted benzamides of the formula:
wherein groups R 2 ′ R 3 ′, R 4 ′ and R 5 ′ can independently be H, alkyl groups having from about 1 to 10 carbons, alkoxyl groups, hydroxyl or halogens, or nitro NO 2 ; or benzimidazolone amides of the formula:
where FM represents SO 3 H, CO 2 H, or —C(═O)—NH-Aryl-SO 3 − where the aryl group can be unsubstituted or substituted with either halogens, or alkyl groups having from about 1 to about 10 carbons, CO 2 H, halogens, NH 2 , or —C(═O)—NH 2 groups, and R 3 and R 4 independently represent H, or SO 3 H;
where FM represents SO 3 H, CO 2 H, or —C(═O)—NH-Aryl-SO 3 − where the aryl group can be unsubstituted or substituted with either halogens, or alkyl groups having from about 1 to about 10 carbons, CO 2 H, halogens, NH 2 , or —C(═O)—NH 2 ; and R 1 , R 2 , R 3 and R 4 independently represent H, SO 3 H, or —C(═O)—NH-Phenyl;
where G represents CO 2 H, straight or branched alkyl having from 1 to about 10 carbons atoms; and R 1 ′, R 2 ′, R 3 ′ and R 4 ′ independently represent H, halogens, SO 3 H, nitro (NO 2 ) or alkoxyl groups; and
where R 1 ′ represents a straight or branched alkyl group having from 1 to about 10 carbon atoms, R 2 ′ represents
where each of R a , R b , and R c independently represents H, a straight or branched alkyl group having from 1 to about 10 carbon atoms, OCH 3 , or halogens.
20. A process for preparing nanoscale-sized monoazo laked pigment particles, comprising:
preparing a first reaction mixture comprising: (a) a diazonium salt having at least one functional moiety as a first precursor to the laked pigment and (b) a liquid medium containing diazotizing agents; and
preparing a second reaction mixture comprising: (a) a coupling agent having at least one functional moiety as a second precursor to the laked pigment and (b) a sterically bulky stabilizer compound having one or more functional groups that associate non-covalently with the coupling agent; and (c) a liquid medium
combining the first reaction mixture into the second reaction mixture to form a solution and
effecting a direct coupling reaction which forms a monoazo laked pigment composition wherein the functional moiety associates non-covalently with the functional group and having nanoscale particle size.
21. The process of claim 20 , wherein the second reaction mixture further comprises one or more additives selected from the group consisting of inorganic and organic buffers, alkaline bases, and acids.
22. The process of claim 20 , wherein the combining is conducted at ambient temperature with high-speed stirring.
23. A process for preparing nanoscale monoazo laked pigment particles, comprising:
providing a monoazo precursor dye to the monoazo laked pigment that has at least one functional moiety;
subjecting the monoazo precursor dye to an ion exchange reaction with a metal cation salt in the presence of a sterically bulky stabilizer compound having one or more functional groups; and
precipitating the monoazo laked pigment as nanoscale particles, wherein the functional moiety of the pigment associates non-covalently with the functional group of the stabilizer and having nanoscale particle size.
24. An ink composition comprising:
a carrier, and
a colorant comprising a nanoscale pigment particle composition according to claim 1 .
25. The ink composition of claim 24 , wherein the carrier is present in an amount of about 50 to about 99.9 weight %, and said colorant is present in an amount of about 0.1 to about 50 weight % by weight of the ink.
26. The ink composition of claim 24 , wherein the carrier comprises one or more organic compounds that are solid at room temperature but becomes liquid at a printer operating temperature for ejecting the ink composition onto a print surface.
27. The ink composition of claim 24 , wherein the carrier is selected from the group consisting of amides, isocyanate-derived resins and waxes, paraffins, microcrystalline waxes, polyethylene waxes, ester waxes, amide waxes, fatty acids, fatty alcohols, fatty amides, sulfonamide materials, resinous materials made from different natural sources, and synthetic resins, oligomers, polymers and copolymers, and mixtures thereof.
28. The ink composition of claim 24 , wherein the carrier comprises a curable material selected from the group consisting of radiation curable monomers, radiation curable oligomers, radiation curable polymers, and mixtures thereof, that is liquid at room temperature.
29. The ink composition of claim 24 , wherein the ink composition is selected from the group consisting of solid ink compositions, phase change ink compositions, curable ink compositions, aqueous ink compositions, and non-aqueous ink compositions.
30. The ink composition of claim 24 , further comprising at least one additive selected from the group consisting of surfactants, light stabilizers, UV absorbers, optical brighteners, thixotropic agents, dewetting agents, slip agents, foaming agents, antifoaming agents, flow agents, oils, plasticizers, binders, electrically conductive agents, fungicides, bactericides, organic and inorganic filler particles, leveling agents, opacifiers, antistatic agents, dispersants, and mixtures thereof.
31. The ink composition of claim 24 , where the colorant consists of said nanoscale pigment particle composition, and said nanoscale pigment particle composition is the only colorant present in the ink composition.
32. The ink composition of claim 24 , where the colorant comprises said nanoscale pigment particle composition and at least one other colorant material.