WO1997048769A1 - Colored pigment and aqueous compositions containing same - Google Patents

Colored pigment and aqueous compositions containing same Download PDF

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Publication number
WO1997048769A1
WO1997048769A1 PCT/US1997/009862 US9709862W WO9748769A1 WO 1997048769 A1 WO1997048769 A1 WO 1997048769A1 US 9709862 W US9709862 W US 9709862W WO 9748769 A1 WO9748769 A1 WO 9748769A1
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WO
WIPO (PCT)
Prior art keywords
group
pigment
colored pigment
salt
modified
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Ceased
Application number
PCT/US1997/009862
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English (en)
French (fr)
Inventor
Joseph E. Johnson
James A. Belmont
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Cabot Corp
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Cabot Corp
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Filing date
Publication date
Application filed by Cabot Corp filed Critical Cabot Corp
Priority to AU32328/97A priority Critical patent/AU3232897A/en
Priority to EP97928007A priority patent/EP0906371B1/en
Priority to JP50307698A priority patent/JP4138882B2/ja
Priority to DE69711040T priority patent/DE69711040T2/de
Publication of WO1997048769A1 publication Critical patent/WO1997048769A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00—Inks
    • C09D11/30—Inkjet printing inks
    • C09D11/32—Inkjet printing inks characterised by colouring agents
    • C09D11/322—Pigment inks
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0001—Post-treatment of organic pigments or dyes
    • C09B67/0004—Coated particulate pigments or dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/41—Organic pigments; Organic dyes
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00—Developers
    • G03G9/08—Developers with toner particles
    • G03G9/09—Colouring agents for toner particles
    • G03G9/0906—Organic dyes

Definitions

  • This invention relates to a colored pigment and aqueous compositions containing the same and, more particularly, to colored ink compositions useful for imaging applications, such as ink jet inks.
  • Aqueous systems are increasingly being used in many applications such as automotive and industrial coatings, paints, papers, inks, toners, adhesives, latexes, etc. as manufacturers face increased pressure to replace conventional solvent based systems.
  • aqueous systems are known and generally contain a colorant, such as a dye or polymer/surfactant stabilized pigment, which is soluble in the aqueous vehicle, such as water or a mixture of water and a water-soluble or water-miscible organic solvent.
  • dyes have several disadvantages when used in, for example aqueous ink systems.
  • dyes being water-soluble in a water/organic mixture, may dissolve and run when exposed to moisture or water.
  • Dye images may further smear or rub off on contact with felt pen markers or upon being rubbed or touched by finger.
  • Dyes also exhibit poor light stability when expose to visible or ultraviolet light.
  • Pigments are also known as colorants in aqueous compositions but have not received a wide degree of acceptance in aqueous systems, such as ink jet inks, because of problems associated with the performance and reliability of the composition, i.e., print properties, stability, latency, and the like. Examples of such pigments include carbon black, titanium dioxide white, cobalt blue (CoO-Al 2 O 3 ), phthalocyanine blue, phthalocyanine green, and chrome yellow (PbCrO 4 ).
  • aqueous compositions are suitable for their intended purpose, a need remains for improved aqueous compositions, especially for use in the ink jet printers, which overcome the problems typically associated with current dye-based and pigment systems.
  • the present invention relates to a surface- modified, colored pigment having at least one attached hydrophilic organic group.
  • the colored pigment has no primary amines.
  • a method of preparing the surface-modified, colored pigment having at least one attached hydrophilic organic group is also disclosed. The process comprises the step of reacting at least one diazonium salt with a colored pigment, preferably in a protic reaction medium.
  • the present invention is further directed to aqueous compositions comprising a surface-modified colored pigment having at least one attached hydrophilic organic group.
  • aqueous compositions comprising a surface-modified colored pigment having at least one attached hydrophilic organic group.
  • an ink composition comprising a surface-modified, color pigment having at least one attached hydrophilic organic group.
  • the surface-modified color pigment of the present invention may be used in aqueous compositions containing conventional pigments.
  • aqueous compositions include, for example, automotive and industrial coatings, paints, papers, toners, inks, adhesives, latexes, textiles and fibers.
  • the surface-modified colored pigment may be tailored to provide compatibility with the particular aqueous system and provide easier, more complete dispersion, improved colloidal stability and greater color intensity and shades.
  • Figure 1 is a graph of the wavelength (nm) on the x-axis versus absorbance on the y-axis for a surface-modified phthalocyanine blue (Pigment Blue 15) of the present invention and an untreated phthalocyanine blue (Pigment Blue 15).
  • Figure 2 is a graph of the wavelength (nm) on the x-axis versus absorbance on the y-axis for a surface-modified Paliogen Red Violet L5080 (Pigment Red 88) of the present invention and an untreated Paliogen Red Violet L5080 (Pigment Red 88).
  • Figure 3 is a graph of the wavelength (nm) on the x-axis versus absorbance on the y-axis for a surface-modified Hostaperm Orange GR (Pigment Orange 43) of the present invention and an untreated Hostaperm Orange GR (Pigment Orange 43).
  • Figure 4 is a graph of the wavelength (nm) on the x-axis versus absorbance on the y-axis for a surface-modified Hostaperm Pink E (Pigment Red 122) of the present invention and an untreated Hostaperm Pink E (Pigment Red 122).
  • Figure 5 is a graph of the wavelength (nm) on the x-axis versus absorbance on the y-axis for a surface-modified phthalocyanine blue (Pigment Blue 15) of the present invention and an untreated phthalocyanine blue (Pigment Blue 15).
  • the present invention relates to a surface-modified, colored pigment having at least one attached hydrophilic organic group.
  • the colored pigment has no primary amines and, preferably, at least one aromatic ring in its repeating structure to promote the modification of the organic group to the surface of the pigment.
  • a wide range of conventional colored pigments may be used in the present invention provided that such pigments do not possess a primary amine.
  • the colored pigment can be blue, brown, cyan, green, violet, magenta, red, yellow, as well as mixtures thereof.
  • Suitable classes of colored pigments include, for example, anthraquinones, phthalocyanine blues, phthalocyanine greens, diazos, monoazos, pyranthrones, perylenes, heterocyclic yellows, quinacridones, and (thio)indigoids.
  • Representative examples of phthalocyanine blues include copper phthalocyanine blue and derivatives thereof (Pigment Blue 15).
  • quinacridones include Pigment Orange 48, Pigment Orange 49, Pigment Red 122, Pigment Red 192, Pigment Red 202, Pigment Red 206, Pigment Red 207, Pigment Red 209, Pigment Violet 19 and Pigment Violet 42.
  • anthraquinones include Pigment Red 43, Pigment Red 194 (Perinone Red), Pigment Red 216 (Brominated
  • Pigment Red 226 Pyranthrone Red
  • Pigment Red 226 Pigment Red 226
  • Representative examples of perylenes include Pigment Red 123 (Vermillion), Pigment Red 149 (Scarlet), Pigment Red 179 (Maroon), Pigment Red 190 (Red), Pigment Violet, Pigment Red 189 (Yellow Shade Red) and Pigment Red 224.
  • Representative examples of thioindigoids include Pigment Red 86, Pigment Red 87, Pigment Red 88, Pigment
  • Pigment Red 181 Pigment Red 198, Pigment Violet 36, and Pigment Violet 38.
  • Representative examples of heterocyclic yellows include Pigment Yellow 117 and Pigment Yellow 138. Examples of other suitable colored pigments are described in the Colour Index, 3rd edition (The Society of Dyers and Colourists, 1982).
  • the hydrophilic organic group of the surface-modified colored pigment has at least one aromatic group, and at least one ionic group or ionizable group.
  • a preferred set of organic groups which may be attached are organic groups substituted with an ionic or an ionizable group as a functional group.
  • An ionizable group is one capable of forming an ionic group in the medium of use.
  • the ionic group may be an anionic group or a cationic group and the ionizable group may form an anion or cation.
  • Ionizable functional groups forming anions include, for example, acidic groups or salts of acidic groups.
  • the organic groups therefore, include groups derived from organic acids.
  • an organic group contains an ionizable group forming an anion, such an organic group has a) an aromatic group and b) at least one acidic group having a pK, of less than 11, or at least one salt of an acidic group having a pK, of less than 11 , or a mixture of at least one acidic group having a pK, of less than 11 and at least one salt of an acidic group having a pK, of less than 11.
  • the pK, of the acidic group refers to the pK, of the organic group as a whole, not just the acidic substituent. More preferably, the pK, is less than 10 and most preferably less than 9.
  • the aromatic group of the organic group is directly attached to the colored pigment. The aromatic group may be further substituted or unsubstituted, for example, with alkyl groups. More preferably, the organic group is a phenyl or a naphthyl group and the acidic group is a sulfonic acid group, a sulfinic acid group, a phosphonic acid group, or a carboxylic acid group.
  • the organic group is a substituted or unsubstituted sulfophenyl group or a salt thereof; a substituted or unsubstituted carboxyphenyl; a substituted or unsubstituted (polysulfo)phenyl group or a salt thereof; a substituted or unsubstituted sulfonaphthyl group or a salt thereof; or a substituted or unsubstituted (polysulfo)naphthyl group or a salt thereof.
  • Such groups include, for example, C 6 H 4 SO 3 -M + , C 6 H 4 CO 2 -M + , wherein M + is Na + , K + , or Li + .
  • Amines represent examples of ionizable functional groups that form cationic groups.
  • amines may be protonated to form ammonium groups in acidic media.
  • an organic group having an amine substituent has a pK j , of less than 5.
  • Quaternary ammonium groups and quaternary phosphonium groups also represent examples of cationic groups.
  • the organic group contains an aromatic group such as a phenyl or a naphthyl group and a quaternary ammonium or a quaternary phosphonium group. The aromatic group is preferably directly attached to the colored pigment. Quatemized cyclic amines, and even quatemized aromatic amines, can also be used as the organic group.
  • N-substituted pyridinium compounds such as N-methyl-pyridyl, can be used in this regard.
  • organic groups include, but are not limited to, C 6 H 4 N(CH 3 ) 3 'f" X " , C 6 H 4 C O C H 2 N ( C H 3 ) 3 + X- , C 6 H 4 (N C 5 H 5 ) + ⁇ - , ( C 5 H 4 N ) C 2 H 5 + ⁇ - , C 6 H 4 COCH 2 (NC 5 H 5 ) + X-, (C 5 H 4 N)CH 3 + X " , and C 6 H 4 CH 2 N(CH 3 ) 3 + X " , wherein X ' is a monovalent ion.
  • the colored pigment of the present invention is subjected to a surface treatment which attaches the hydrophilic organic group to the aromatic moieties of the colored pigment.
  • the attachment reaction involves the use of a primary amine from the hydrophilic organic group.
  • the absence of a primary amine from the colored pigment is essential to providing adequate surface modification and prevent decomposition of the colored pigment itself.
  • the surface-modified colored pigment may be prepared by the methods described in U.S. Patent Application Serial No. 08/356,653 to Belmont entitled, "Reaction of Carbon Materials with Diazonium Salts and Resultant Carbon Products," filed December 15, 1994; U.S. Patent Application No. 08/356,660, to Belmont entitled, "Reaction of Carbon Black with Diazonium Salts, Resultant Carbon Black Products and Their Uses,” filed December 15, 1994; and
  • the process is carried out in a protic medium, such as water, at a pH less than 7, more preferably at a pH of about 2.
  • a protic medium such as water
  • the reaction temperature is between about -10°C and about 100°C, more preferred between 40°C and about 70°C, and especially preferred at 70 C C.
  • the surface-modified color pigment of the present invention may be used in aqueous compositions containing conventional pigments.
  • the following relating to ink compositions is similarly applicable to other aqueous systems including, for example, coatings, papers, paints, inks, toners, adhesives, latexes, textiles and fibers.
  • Ink compositions of the present invention comprise a surface-modified colored pigment having at least one attached hydrophilic organic group.
  • the ink compositions are suitable for use in imaging applications, such as ink jet inks.
  • the ink compositions of the present invention further exhibit improved latency and the images generated therefrom exhibit improved waterfastness.
  • the surface-modified colored pigment of the present invention is present in the ink compositions in an amount effective to provide the desired image quality, e.g., optical density, without detrimentally affecting the performance of the ink.
  • the surface-modified colored pigment will be present in an amount ranging from about 1 % to about 20%, preferably from about 2% to about 10% , based on the weight of the ink composition.
  • the surface-modified colored pigment should be treated with the desired modifying agent in an amount sufficient to provide the desired utility in the end product application while maintaining the colloidal stability of the pigment in the ink composition.
  • the surface-modified colored pigment is typically as small as possible to enable a stable colloidal suspension of the pigment in the liquid vehicle and to prevent clogging of the ink channels and nozzles when used in the desired printing application.
  • a preferred average aggregate diameter of the surface- ' modified colored pigment for use in a thermal inkjet printer are generally below 1.0 micron, preferably in a range from about 0.005 micron to about 0.3 micron.
  • the ink compositions of the present inventions may be prepared utilizing conventional techniques known to those skilled in the art, such as combining or mixing the desired component in a suitable medium.
  • the ink compositions are aqueous systems and, as such, include a significant amount of water, preferably deionized or distilled water.
  • the amount of water or similar medium is generally present in an amount ranging from about 50% to about 95% , preferably from about 60% to 80% , based on the weight of the ink composition.
  • the ink compositions of the present invention may be buffered to the desired pH by the addition of a suitable base, such as sodium hydroxide, ammonium hydroxide, triethylamine, dimethylethanolamine and the like, or a suitable acid, such as mineral acids, hydrochloric acid, sulfuric acid and the like.
  • a suitable base such as sodium hydroxide, ammonium hydroxide, triethylamine, dimethylethanolamine and the like
  • a suitable acid such as mineral acids, hydrochloric acid, sulfuric acid and the like.
  • a polymer which is soluble in the ink composition may be added to improve the waterfastness of the images generated from the ink compositions.
  • soluble is meant that the polymer will dissolve in the ink vehicle to form a one phase system.
  • polymers include, for example, polyvinyl alcohol, polyester, polyestermelamine, styrene-acrylic acid copolymers, styrene-maleic acid copolymers, styrene-maleic acid-alkyl acrylate copolymers, styrene-metacrylic acid copolymers, styrene-metacrylic acid-alkyl acrylate copolymers, styrene-maleic half ester copolymers, vinyl napthalene-acrylic acid copolymers, vinyl napthalene-maleic acid copolymers and salts thereof.
  • Additional polymers include polyvinylimidazole, derivatives of polyvinylimidazole, copolymers of vinylimidazole, copolymers of vinylimidazole derivatives, polyvinylpyridine, derivatives of polyvinylpyridine, copolymers of vinylpyridine, copolymers of vinylpyridine derivatives, polyethyleneimine, derivatives of polyethyleneime, and mixtures thereof, as described in U. S. Patent Application Serial No. 08/628,202 to Bates et al., entitled “Ink Compositions and Method of Generating Images Produced Therefrom," the disclosure of which is fully inco ⁇ orated herein by reference.
  • Suitable additives are also generally incorporated into the ink compositions to impart a number of desired properties while maintaining the stability of the compositions.
  • a surfactant or suitable polymer may be used to enhance the colloidal stability of the colored pigment in the ink composition.
  • Other additives are well known in the art and include humectants, biocides, binders, drying accelerators, penetrants and the like.
  • humectants include ethylene glycol, propylene glycol, diethylene glycols, glycerine, dipropylene glycols, polyethylene glycols, polypropylene glycols, alkane diols, amides, ethers, carboxylic acids, esters, alcohols, organosulfides, organosulfoxides, sulfones, alcohol derivatives, 2-pyrrolidone, ether derivatives, amino alcohols, and ketones.
  • the amount of a particular additive will vary depending on a variety of factors but are generally present in an amount ranging between 0% and 10%, preferably between 0.1 % and 5% , although the amount may be outside this range.
  • Printed images may be generated from the ink compositions of the present invention by incorporating such compositions into a suitable printing apparatus, and generating an image onto a substrate.
  • Suitable inkjet printers include, for example, thermal printers, piezoelectric printers, continuous printers, valve printers and the like.
  • any suitable substrate can be employed including plain papers, bonded papers, coated papers, transparency materials, textile materials, plastics, polymeric films, inorganic substrates and the like.
  • the surface-modified color pigment may be used in other aqueous systems including, but not limited to, coatings, paints, papers, adhesives, latexes, toners, textiles and fibers.
  • the aqueous systems may be prepared by combining or mixing the surface-modified color pigment with suitable waterbome resins, such as alkyds, acrylics, polyesters, silicates, urethanes, epoxies and the like.
  • the samples of the surface-modified colored pigment were chemically analyzed using spectrophometric and/or titration reaction, to determine the sulfur content resulting from the sulfonate addition reaction. Carbon, hydrogen and nitrogen were also determined by a combustion technique using a Fissions EA-1108 gas chromatograph instrument.
  • the zeta potential at a pH of 6 of a 5 mg/ml concentration of the modified colored pigment in a 0.0010 M NaCl aqueous medium was determined using a Brookhaven Zeta-Plus Instrument, Holtsville, New York.
  • Zeta potential (f) is the potential difference, measured in a liquid, between the shear plane and the bulk of the liquid beyond the limits of the electrical double layer at the surface of the colored pigment.
  • the zeta potential will be dependent on the type of surface groups of the modified colored pigment, in addition to the amount and type of ions in an aqueous medium.
  • an absorbance spectra of modified color pigment at a 0.010%, by weight, concentration in distilled water were taken using a Perkin-Elmer Visible Model Lambda 6 UV/Vis spectrophotometer.
  • the sulfur content, carbon content, hydrogen content, nitrogen content and zeta potential was also determined for the untreated Pigment Blue 15.
  • the sulfur content, nitrogen content and zeta potential of the modified color pigment and the untreated pigment was illustrated in Table 1.
  • the absorbance spectra of the surface-modified colored pigment and the untreated pigment is represented in Figure 1. Table 1
  • the addition of the sulfanilic acid with nitrite under acidic conditions resulted in the attachment of hydrophilic, sulfur-containing groups to the pigment, as noted in the increase in sulfur content.
  • the decrease in carbon, hydrogen and nitrogen further indicates that chemical modification of the pigment took place.
  • the difference in the zeta potentials show that the surface groups of the pigments are different in charge and magnitude in similar aqueous mediums.
  • the difference in the zeta potentials illustrate that the surface reaction/attachment is taking place at the surface of the colored pigment.
  • the larger absolute value of the zeta potential indicates a more colloidal stable system, while the negative charge indicates that the anionic nature of the surface group, i.e. sulfonate, on the pigment surface.
  • the absorbance plots of Figure 1 demonstrate that the pigments vary in degree of dispersibility or affinity for water.
  • the increase in absorbance throughout the wavelength range indicates that the surface-modified colored pigment was more readily dispersed in water using, for example, mild stirring such as shaking by hand.
  • the untreated pigment on the other hand, was very difficult to disperse in water, -and agglomerated, i.e. clumped, upon standing in a short period of time.
  • phthalocyanine pigments will also be suitable for surface modification, provided they have at least one available aromatic site.
  • a surface-modified phthalocyanine blue pigment was prepared by repeating the procedure of Example 1 except that the amount of sulfanilic acid was varied at 0.60 and 2.0 grams and the amount of sodium nitrite was also varied at 0.25 and 0.84 grams, respectively.
  • the sulfur content and zeta potential of the modified color pigment and the untreated pigment is illustrated in Table 2.
  • a surface-modified phthalocyanine blue pigment was prepared by repeating the procedure of Example 1 except that the treatment was at 40°C, instead of 70°C.
  • the sulfur content and zeta potential of the surface-modified color pigment and the untreated pigment is illustrated in Table 3.
  • a surface-modified phthalocyanine blue pigment was prepared by repeating the procedure of Example 1 except that the hydrochloric acid was omitted.
  • the sulfur content and zeta potential of the surface-modified color pigment and the untreated pigment is illustrated in Table 4.
  • Table 4 illustrates that sulfonate addition reaction may take place in an acidic media without adjusting the pH with an acid. The result is a surface-modified color pigment which is more readily dispersible and colloidally stable in an aqueous medium.
  • a surface-modified indigoid pigment was prepared by repeating the procedure of Example 1 except that Paliogen Red Violet L5080 (Pigment Red 88, Cl # 73312, available from BASF Corporation, Rensselaer, NY) was used instead of the phthalocyanine blue.
  • the sulfur content and zeta potential of the surface-modified color pigment and the untreated pigment was illustrated in Table 5.
  • the absorbance spectra of the surface-modified colored pigment and the untreated pigment is represented in Figure 2.
  • Table 3 illustrates that there was no discernible difference in sulfur content between the modified color pigment and untreated pigment, the difference in zeta potential and absorbance spectra indicate the surface of the pigment was modified upon treatment. The result was a modified color pigment which was easily dispersed in distilled water upon vortexing.
  • a surface-modified anthraquinone pigment was prepared by repeating the procedure of Example 1 except that Hostaperm Orange GR (Pigment Orange 43, Cl # 71105, available from Hoechst Celanese, Charlotte, NC) was used instead of the phthalocyanine blue.
  • Hostaperm Orange GR Pigment Orange 43, Cl # 71105, available from Hoechst Celanese, Charlotte, NC
  • the sulfur content and zeta potential of the surface-modified color pigment and the untreated pigment is illustrated in Table 6.
  • the absorbance spectra of the surface-modified colored pigment and the untreated pigment is represented in Figure 3.
  • a surface-modified quinonoid (also known as a quinacridone) pigment was prepared by repeating the procedure of Example 1 except that Hostaperm Pink E pigment (Pigment Red, 122, Cl # 73915 available from Hoechst Celanese, Charlotte, NC) was used instead of the phthalocyanine blue.
  • Hostaperm Pink E pigment Pigment Red, 122, Cl # 73915 available from Hoechst Celanese, Charlotte, NC
  • the sulfur content and zeta potential of the modified color pigment and the untreated pigment is illustrated in Table 7.
  • the absorbance spectra of the surface-modified colored pigment and the untreated pigment, both at 0.0020% by weight concentration, is represented in Figure 4.
  • a surface-modified phthalocyanine blue pigment was prepared by repeating the procedure of Example 1 except that N-(4-aminophenyl)pyridium chloride was used instead of the sulfanilic acid.
  • the nitrogen content and zeta potential of the surface- modified color pigment and the untreated pigment is illustrated in Table 8.
  • the absorbance spectra of the surface-modified colored pigment and the untreated pigment, is represented in Figure 5.
  • the surface modified pigment of Example 1 was added to distilled water to form an aqueous dispersion at a 20% loading level, by weight, of pigment.
  • the dispersion was filtered to below 5 microns and formulated into an ink jet ink having the following components, by weight: 7% surface-modified Pigment Blue 15, 63% distilled water, and 30% glycerol.
  • Tristimulus color values L*, a* and b*, were determined using a Hunter Lab Scan II Instrument, as indicated in Table 9. The values were obtained before and after washing the pigment for approximately 1 minute with distilled water and redrying.
  • the surface-modified organic pigment of the present invention may be useful in a wide variety of aqueous based applications and, in particular, ink compositions to provide the desired color and intensity. Unlike conventional pigments, the surface-modified color pigment is readily dispersed in the desired liquid vehicle requiring only low shear mixing or stirring. In addition, the surface-modified color pigment has a higher absolute zeta potential value and greater stability when compared to an untreated pigment.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
PCT/US1997/009862 1996-06-17 1997-05-23 Colored pigment and aqueous compositions containing same Ceased WO1997048769A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
AU32328/97A AU3232897A (en) 1996-06-17 1997-05-23 Colored pigment and aqueous compositions containing same
EP97928007A EP0906371B1 (en) 1996-06-17 1997-05-23 Colored pigment and aqueous compositions containing same
JP50307698A JP4138882B2 (ja) 1996-06-17 1997-05-23 着色顔料およびそれを含む水性組成物
DE69711040T DE69711040T2 (de) 1996-06-17 1997-05-23 Farbpigment und wässrige zusammensetzungen die dieses pigment enthalten

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US08/664,455 US5837045A (en) 1996-06-17 1996-06-17 Colored pigment and aqueous compositions containing same
US08/664,455 1996-06-17

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EP (1) EP0906371B1 (enExample)
JP (1) JP4138882B2 (enExample)
AU (1) AU3232897A (enExample)
DE (1) DE69711040T2 (enExample)
TW (1) TW426716B (enExample)
WO (1) WO1997048769A1 (enExample)
ZA (1) ZA974680B (enExample)

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WO2000052102A1 (en) * 1999-03-05 2000-09-08 Cabot Corporation Process for preparing colored pigments
EP1061107A1 (en) * 1999-06-18 2000-12-20 Hewlett-Packard Company Superior waterfastness and bleed control with specifically treated pigments for ink-jet printing
EP1061106A1 (en) * 1999-06-18 2000-12-20 Hewlett-Packard Company Ink-jet printing inks containing ester modified macromolecular chromophores
US6177485B1 (en) 1999-02-17 2001-01-23 Hewlett-Packard Company Polymers derived from unsaturated surfactants for use in ink-jet inks
WO2001010963A1 (en) * 1999-08-09 2001-02-15 Cabot Corporation Ink compositions having modified pigments with high or low treatment levels
US6214100B1 (en) 1999-06-18 2001-04-10 Hewlett-Packard Company Ink-jet printing inks containing ester modified macromolecular chromophores
US6221143B1 (en) 1999-03-12 2001-04-24 Cabot Corporation Cationic pigments and aqueous compositions containing same
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EP0906371A1 (en) 1999-04-07
TW426716B (en) 2001-03-21
AU3232897A (en) 1998-01-07
ZA974680B (en) 1997-12-30
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US5837045A (en) 1998-11-17

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