[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

US20040167250A1 - Novel toner compositions for black gravure inks - Google Patents

Novel toner compositions for black gravure inks Download PDF

Info

Publication number
US20040167250A1
US20040167250A1 US10/749,446 US74944603A US2004167250A1 US 20040167250 A1 US20040167250 A1 US 20040167250A1 US 74944603 A US74944603 A US 74944603A US 2004167250 A1 US2004167250 A1 US 2004167250A1
Authority
US
United States
Prior art keywords
black
gravure ink
ink solution
inks
gravure
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/749,446
Inventor
Rajnish Batlaw
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US10/749,446 priority Critical patent/US20040167250A1/en
Publication of US20040167250A1 publication Critical patent/US20040167250A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/03Printing inks characterised by features other than the chemical nature of the binder
    • C09D11/037Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M7/00After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
    • B41M7/009After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using thermal means, e.g. infrared radiation, heat
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24802Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]

Definitions

  • a novel, easy, and efficient manner of toning shades of toluene-based gravure inks is provided, particularly through the incorporation of certain polymeric colorants therein said gravure ink formulations.
  • toner additives provide toning capabilities of carbon black-based gravure inks that provides jetter black appearances with lower degrees of redness and bronzing on various types of printing substrates than other toner formulations with standard alkali blue types of toning additives.
  • Such printed substrates and methods of printing utilizing such novel gravure toner additives are also encompassed within this invention.
  • Toners are necessary to provide jet black appearances of inks containing standard black pigments, such as, carbon black, as one prominent example.
  • Such a toner must be compatible in gravure ink vehicles, must not alter the mobility, the low viscosity, and the fundamental fast drying properties of the ink necessary for the Gravure process.
  • alkali blue from BASF, known as Pigment 61 (Colour Index # 42765:1) is utilized as the most prevalent black pigment toner in such gravure ink operations.
  • U.S. Pat. No. 4,383,865 discloses a process for preparing a soft textured, high strength Alkali Blue pigment composition which comprises insolubilized amines.
  • This composition is made by mixing a solution of alkali blue crude first with an alkaline solution of an alkyl aryl sulfonic acid, then with an acidic solution having from 3 to 36 carbon atoms, following which the pigment composition is recovered.
  • the preferred group of alkyl aryl sulfonic acids has from 1 to 14 carbon atoms. The most preferred alkyl aryl sulfonic acid appears to be dodecylbenzene sulfonic acid.
  • U.S. Pat. Nos. discloses a particular combination of surfactants, when incorporated with an Alkali Blue Pigment 61, produce a pigment product having the desirable characteristic of exhibiting high strength when used in either water flexo or oil ink end uses.
  • the surfactants utilized are (1) di- and tri-decyl phosphate esters of free acids, together with (2) dehydroabietyl amine.
  • U.S. Pat. No. 4,032,357 assigned to Sherwin-Williams Company, discloses a substantially anhydrous, free-flowing alkali blue pigment composition having an organic anionic dispersant coprecipitated therewith. Furthermore, the pigment and dispersant are admixed with an oil phase in order to reduce the hydrophilic aggregation of the coprecipitated pigment and dispersant.
  • the specific organic dispersants used in the '357 patent are Gafac.RTM. RS-710 and Gafac.RTM. RS-610.
  • U.S. Pat. No. 5,026,627 disclose a particular combination of surfactants when incorporated with an alkali blue pigment, produce a pigment toner exhibiting high strength when used in toluene-based inks (as one example of gravure types). While the pigment is widely used throughout the industry, they have serious drawbacks (as discussed above) in that they are difficult to handle, they are not conducive to post addition, provide a reddish tone to carbon black and causes bronzing of the printed image.
  • one of the objects of the invention is to provide a toluene-soluble colorant.
  • Another object of the invention is to provide a colorant that can be used as a toner for toluene-based (gravure) inks.
  • Yet another object of the invention is to provide a colorant that can tone carbon black based inks to give a jet-black image without an appreciable degree of noticeable reddening and/or bronzing.
  • Still another object of the invention is to provide a colorant that can tone carbon black based inks to give a glossier image.
  • Yet another object of the invention is to provide a colorant that can tone carbon black based inks to give an image with substantially reduced bronzing.
  • the colorants according to the invention are notable for very wide compatibility with the binder and printing ink systems customary for printing processes, such as Gravure, in single-color or multi-color printing. They are, for example, easily incorporated in binder systems for toluene-based inks.
  • the printing inks with the colorants according to the invention are satisfactorily printable and produce strong bright prints.
  • the colorants according to the invention are also suitable for mixing with carbon black in order to produce printing inks that, upon printing, produce an excellent brightening and jetting effect on the target substrate.
  • the colorants are also suitable for producing printing inks for copy papers and ink ribbons, and as coloring agents in toners for electrophotographic printing.
  • the actual printed substrates including, without limitation, paper, cardboard, paperboard, and other like cellulosic- or synthetic-based substrates, films and other plastic substrates, and textiles, such as fabrics made from natural fibers, such as cotton, linen, ramie, and the like, synthetic fibers, such as polyester, polyamide, polyaramid, and the like, and inorganic fibers, such as fiberglass, boron-derived fibers, glass
  • the ink compositions of the present invention are toluene solutions of one or more colorants.
  • the colorants can be used to tone shades of toluene based inks to obtain desired look of the printed image. It is also an advantage of the present invention that the colorants can be added to the toluene-based inks at any stage during the manufacture or use of the inks. It is another advantage of the present invention that the colorants can be used in combination with other toluene based ink carrier materials to obtain ink compositions that possess excellent spectral strengths. It is still another advantage of the present invention that the colorants are substantially transparent. It is yet another advantage of the present invention that the colorants can be used to tone carbon black based inks to provide jet blacks. It is yet another advantage of the present invention that the colorants are easy to handle in production.
  • the standard alkali blue pigment used in the industry tones the carbon black based toluene ink providing a reddish tone (higher ‘a’ values), and a bronzing effect on the printed image. Furthermore, the alkali blue pigment is very difficult to handle in production and can be added to the carbon black based inks only during the manufacture of the inks.
  • the inventive colorants therefore provide clear distinct advantages over the alkali blue and other blue and magenta pigments used.
  • the particular toning components utilized within these inventive gravure ink compositions are polymeric (e.g., polyoxyalkenylated) colorants that exhibit ⁇ circle over (2) ⁇ max absorption measurements between about 550 and 610 nm (wavelengths), most preferably wavelengths between about 560 and 580 nm.
  • polymeric colorants must include nonionic chromophores as the coloring portion of the colorant itself.
  • azos, anthraquinones, indigoids, benzodifuranones, and the like may be utilized as the chromophoric component of the desired polymeric colorant.
  • Such a selection criteria is significantly better for gravure ink compositions because such inks require the utilization of non-polar solvents therein.
  • ionic (cationic, anionic, for example) chromophores affects the toning of the colorant within the gravure ink composition.
  • chromophores of triphenylmethanes and other ionic species are significantly less effective as toners for gravure inks.
  • the polyoxyalkylene chains of such a particular polymeric colorant must comprise at least a majority of propylene oxide in order to provide the necessary level of solvent solubility for proper stability and compatibility within gravure inks (such as within toluene, as the primary non-limiting example).
  • the polyoxyalkylene chains of such a particular polymeric colorant must comprise at least a majority of propylene oxide in order to provide the necessary level of solvent solubility for proper stability and compatibility within gravure inks (such as within toluene, as the primary non-limiting example).
  • polyoxyalkylene chains of all propylene oxide, or all such C 3 and higher alkylene oxides is possible; however, more preferable is a range of ratios of ethylene oxide to such C 3 or higher alkylene oxides of from about 1:1.4 to about 1:4; more preferably from about 1:1.4 to about 1:3; and most preferably from about 1:1.4 to about 1:2; with, as noted above, propylene oxide the most preferred C 3 or higher alkylene oxide monomer present therein.
  • polymeric colorants such as MILLIJET® Violet X80 (an azo-based polymeric colorant, available from Milliken & Company) and other like nonionic chromophore-based polymeric colorants exhibiting ⁇ circle over (2) ⁇ max absorption measurements between the necessary wavelengths as noted above, are proper for this invention.
  • Such gravure inks typically comprise (all in terms of weight percent within the total formulation) from 4-12% of a pigment and/or dyestuff (most prevalently carbon black or furnace black), from 0-8% of an extender pigment (such as alumina, calcium carbonate, and china clay), from 10 to 30% of a resin component (such as, most commonly modified resins, such as cellulose, polyamides, acrylic, vinyl, and/or hydrocarbon soluble resins), from 40 to 60% of a solvent (such as, most commonly toluene, while others, such as ketones, like methyl ethyl ketone, alcohols, like isopropyl alcohol, and esters, like ethyl acetate, as examples), and other additives, such as plasticizers, waxes and other types of like components, in amounts of from 2 to 10%.
  • a pigment and/or dyestuff most prevalently carbon black or furnace black
  • an extender pigment such as alumina, calcium carbonate, and china clay
  • a resin component such as
  • the amount of toner component present within the inventive ink is from 0.01 to 50 parts per 100 parts of the total composition. Preferably, this amount is from 1 to 20 parts, more preferably from 2 to 15 parts, and most preferably from about 5 to about 10 parts. Surprisingly, it has been realized that higher concentrations (5 parts and higher, more particularly, above 6 parts) provide vast, unexpected improvements in measured hue angle and blueness of the sample inventive ink compositions. As noted below in greater detail, the blueness and corresponding hue angle are desirous and are surprisingly attained through the utilization of the inventive or otherwise selected toner components.
  • Chroma is the amount of pure color contained in the sample, and is graphically measured (in CIELAB and/or CMC terms) as the distance from the center of the a* and b* axis for the sample. Brightness is a measurement of such a value for the particular sample of color. Hue angle is a measurement in terms of chroma as it is perceived by the viewer. A color difference between two distinct point on the axis can thus be described as the difference in each points' brightness (L*) value, the difference in their chroma (c*) value, and the difference in their hue angle (h*).
  • Hue is measured in degrees from 0 to 360 (or a correlated negative angle on a Cartesian graph), where red is represented at the 0 angle, yellow at 90, green at 270 (or ⁇ 90, for example), and blue at 360.
  • the hue attribute of visual sensation has given rise to the color names (e.g., blue, green, yellow, red, etc.).
  • Hue differences then depend primarily on variations in the wavelength of light reaching the eye at a particular angle from the viewed sample. Such a measurement (hue angle) is thus one of the three standard elements of color appearance (with the other two being brightness and saturation, or chroma, as noted above).
  • Its colorimetric equivalent is dominant wavelength and, in terms of this invention, is of utmost importance, particularly for black offset inks, in providing a more effective, jetter, less red, less bronze, black ink.
  • the target of this invention is thus to provide a hue angle closer to that of a typical blue measurement within the inventive ink after being drawn down on a surface.
  • a hue angle measurement closer to the blue angle, or alternatively, further from the typical red angle, is thus the unexpected beneficial characteristic of these inventive inks, particularly as compared with the inks of the prior art comprising the state of the art in toning components (alkali blue pigment 61, etc., as discussed above).
  • the inventive inks exhibited vastly improved and unexpectedly good measurements, particularly for hue angle, as compared with the standard alkali blue-containing inks.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Thermal Sciences (AREA)
  • Toxicology (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • General Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Developing Agents For Electrophotography (AREA)

Abstract

A novel, easy, and efficient manner of toning shades of toluene-based gravure inks is provided, particularly through the incorporation of certain polymeric colorants therein said gravure ink formulations. In addition, such toner additives provide a toning capabilities of carbon black-based gravure inks that provides jetter black appearances with lower degrees of redness and bronzing on various types of printing substrates than other toner formulations of standard alkali blue types of toning additives. Such printed substrates and methods of printing utilizing such novel gravure toner additives are also encompassed within this invention.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation of co-pending application No. 10/001,347, filed on Oct. 26, 2001.[0001]
  • FIELD OF THE INVENTION
  • A novel, easy, and efficient manner of toning shades of toluene-based gravure inks is provided, particularly through the incorporation of certain polymeric colorants therein said gravure ink formulations. In addition, such toner additives provide toning capabilities of carbon black-based gravure inks that provides jetter black appearances with lower degrees of redness and bronzing on various types of printing substrates than other toner formulations with standard alkali blue types of toning additives. Such printed substrates and methods of printing utilizing such novel gravure toner additives are also encompassed within this invention. [0002]
  • BACKGROUND OF THE PRIOR ART
  • All U.S. and foreign patents cited within this specification are hereby incorporated by reference. [0003]
  • The nature of the gravure process imposes certain fundamental requirements on the chemical, physical and strength characteristics of the required inks. Toners are necessary to provide jet black appearances of inks containing standard black pigments, such as, carbon black, as one prominent example. Such a toner must be compatible in gravure ink vehicles, must not alter the mobility, the low viscosity, and the fundamental fast drying properties of the ink necessary for the Gravure process. Currently, alkali blue, from BASF, known as Pigment 61 (Colour Index # 42765:1) is utilized as the most prevalent black pigment toner in such gravure ink operations. Unfortunately, although such a toner meets the required solubility properties, the toning effects provided thereby simultaneously are less than satisfactory due to an excessive reddening and/or bronzing of the black printed image. An improved toner reducing such unwanted effects is thus highly desired within the black Gravure ink industry and market. To date, there are no teachings or fair suggestions of such needed improvements provided by and within the pigment for gravure ink prior art. It is believed that certain chromophores with an appropriate pendant group system may not only provide such desired solvent (toluene, ketones, etc) solubility, but may also provide effective toning with low-reddening and low-bronzing levels within such black gravure inks. [0004]
  • U.S. Pat. No. 4,383,865, to Iyengar, discloses a process for preparing a soft textured, high strength Alkali Blue pigment composition which comprises insolubilized amines. This composition is made by mixing a solution of alkali blue crude first with an alkaline solution of an alkyl aryl sulfonic acid, then with an acidic solution having from 3 to 36 carbon atoms, following which the pigment composition is recovered. In the '865 patent the preferred group of alkyl aryl sulfonic acids has from 1 to 14 carbon atoms. The most preferred alkyl aryl sulfonic acid appears to be dodecylbenzene sulfonic acid. [0005]
  • The closest related art of which applicants are aware includes the following U.S. Pat. Nos.: 5,026,627; 4,456,485; 4,383,865; 4,032,357. U.S. Pat. No. 5,026,627 discloses a particular combination of surfactants, when incorporated with an Alkali Blue Pigment 61, produce a pigment product having the desirable characteristic of exhibiting high strength when used in either water flexo or oil ink end uses. The surfactants utilized are (1) di- and tri-decyl phosphate esters of free acids, together with (2) dehydroabietyl amine. U.S. Pat. No. 4,456,485, to Iyengar, discloses a process for preparing easily dispersible high color strength powdered alkali blue pigments by precipitating the pigment in the presence of various acids and/or amines, and/or esters, and/or alcohols, etc., as well as the product of these processes. [0006]
  • U.S. Pat. No. 4,032,357, assigned to Sherwin-Williams Company, discloses a substantially anhydrous, free-flowing alkali blue pigment composition having an organic anionic dispersant coprecipitated therewith. Furthermore, the pigment and dispersant are admixed with an oil phase in order to reduce the hydrophilic aggregation of the coprecipitated pigment and dispersant. The specific organic dispersants used in the '357 patent are Gafac.RTM. RS-710 and Gafac.RTM. RS-610. [0007]
  • A colorant compound having polymer or pre-polymer substituent groups may be synthesized by the reaction of a colorant and a polyisocyanate as disclosed in Cross et al., U.S. Pat. No. 4,284,729; Krutak et al., U.S. Pat. No. 5,194,463; and Beckmann et al., U.S. Pat. No. 5,616,678. [0008]
  • U.S. Pat. No. 5,026,627 disclose a particular combination of surfactants when incorporated with an alkali blue pigment, produce a pigment toner exhibiting high strength when used in toluene-based inks (as one example of gravure types). While the pigment is widely used throughout the industry, they have serious drawbacks (as discussed above) in that they are difficult to handle, they are not conducive to post addition, provide a reddish tone to carbon black and causes bronzing of the printed image. [0009]
  • OBJECTS AND SUMMARY OF THE INVENTION
  • Therefore, one of the objects of the invention is to provide a toluene-soluble colorant. Another object of the invention is to provide a colorant that can be used as a toner for toluene-based (gravure) inks. Yet another object of the invention is to provide a colorant that can tone carbon black based inks to give a jet-black image without an appreciable degree of noticeable reddening and/or bronzing. Still another object of the invention is to provide a colorant that can tone carbon black based inks to give a glossier image. Yet another object of the invention is to provide a colorant that can tone carbon black based inks to give an image with substantially reduced bronzing. Yet another object of the invention is to provide a colorant that can tone carbon black based inks and that is easy to handle. Yet another object of the invention is to provide a colorant that can tone carbon black-based gravure inks at any stage of the ink manufacturing process. [0010]
  • It is thus a further object of the invention to provide a colorant with an ability to tone shades of toluene-based (gravure) inks. The colorants according to the invention are notable for very wide compatibility with the binder and printing ink systems customary for printing processes, such as Gravure, in single-color or multi-color printing. They are, for example, easily incorporated in binder systems for toluene-based inks. The printing inks with the colorants according to the invention are satisfactorily printable and produce strong bright prints. The colorants according to the invention are also suitable for mixing with carbon black in order to produce printing inks that, upon printing, produce an excellent brightening and jetting effect on the target substrate. The colorants are also suitable for producing printing inks for copy papers and ink ribbons, and as coloring agents in toners for electrophotographic printing. [0011]
  • Accordingly, then, this invention encompasses a gravure ink solution comprising at least one polymeric colorant toner component, at least one coloring component selected from the group consisting of at least one pigment, at least one dyestuff, and a mixture of both, at least one solvent, and at least one resin component. Also encompassed within this invention is black gravure ink composition comprising at least one coloring agent selected from the group consisting of at least one black pigment, at least one black dyestuff, and a mixture of both, at least one solvent, at least one resin, and at least one toner component, wherein, when measured under CIELAB and CMC standards, and at a brightness level (L*) of at least 26, said ink exhibits a hue angle (h) of at most 42. Additionally encompassed within this invention is black gravure ink composition comprising at least one coloring agent selected from the group consisting of at least one black pigment, at least one black dyestuff, and a mixture of both, at least one solvent, at least one resin, and at least one toner component, wherein when measured under CIELAB (and/or CMC) standards, and at a brightness level (L*) of at least 26, said ink exhibits an a* level of at most 1.4, a b* level of at most 0.7, and a hue angle (h) of at most 50. Also encompassed within this invention are methods of printing utilizing such ink solutions and the actual printed substrates (including, without limitation, paper, cardboard, paperboard, and other like cellulosic- or synthetic-based substrates, films and other plastic substrates, and textiles, such as fabrics made from natural fibers, such as cotton, linen, ramie, and the like, synthetic fibers, such as polyester, polyamide, polyaramid, and the like, and inorganic fibers, such as fiberglass, boron-derived fibers, glass, and the like, and blends of such fiber types) produced therefrom and therewith. [0012]
  • Without limiting the scope of the invention, the preferred features of the invention are hereinafter set forth. The ink compositions of the present invention are toluene solutions of one or more colorants. [0013]
  • It is an advantage of the present invention that the colorants can be used to tone shades of toluene based inks to obtain desired look of the printed image. It is also an advantage of the present invention that the colorants can be added to the toluene-based inks at any stage during the manufacture or use of the inks. It is another advantage of the present invention that the colorants can be used in combination with other toluene based ink carrier materials to obtain ink compositions that possess excellent spectral strengths. It is still another advantage of the present invention that the colorants are substantially transparent. It is yet another advantage of the present invention that the colorants can be used to tone carbon black based inks to provide jet blacks. It is yet another advantage of the present invention that the colorants are easy to handle in production. [0014]
  • The standard alkali blue pigment used in the industry tones the carbon black based toluene ink providing a reddish tone (higher ‘a’ values), and a bronzing effect on the printed image. Furthermore, the alkali blue pigment is very difficult to handle in production and can be added to the carbon black based inks only during the manufacture of the inks. The inventive colorants therefore provide clear distinct advantages over the alkali blue and other blue and magenta pigments used. [0015]
  • The particular toning components utilized within these inventive gravure ink compositions are polymeric (e.g., polyoxyalkenylated) colorants that exhibit {circle over (2)}[0016] max absorption measurements between about 550 and 610 nm (wavelengths), most preferably wavelengths between about 560 and 580 nm. Furthermore, such polymeric colorants must include nonionic chromophores as the coloring portion of the colorant itself. Thus, azos, anthraquinones, indigoids, benzodifuranones, and the like, may be utilized as the chromophoric component of the desired polymeric colorant. Such a selection criteria is significantly better for gravure ink compositions because such inks require the utilization of non-polar solvents therein. The presence of less compatible ionic (cationic, anionic, for example) chromophores affects the toning of the colorant within the gravure ink composition. Thus, chromophores of triphenylmethanes and other ionic species are significantly less effective as toners for gravure inks.
  • It has also been determined that the polyoxyalkylene chains of such a particular polymeric colorant must comprise at least a majority of propylene oxide in order to provide the necessary level of solvent solubility for proper stability and compatibility within gravure inks (such as within toluene, as the primary non-limiting example). In general, as discussed in such prior art references as U.S. Pat No. 4,812,141 to Baumgartner et al., U.S. Pat. No. 5,176,745 to Moore et al., and U.S. Pat. No. 5,310,887 to Moore et al., polyoxyalkylene chains of polymeric colorants comprise alkylene oxide monomers, such as ethylene oxide, propylene oxide, butylene oxide, and higher carbon chain lengths, as well as possibly glycerol, glyceryl, and other like moieties. The particular limitation found to be important for these toner polymeric colorants is the amount of propylene oxide (or other bulkier oxides, such as butylene oxide or glycerol) must be greater than that for any ethylene oxides present. Thus, polyoxyalkylene chains of all propylene oxide, or all such C[0017] 3 and higher alkylene oxides is possible; however, more preferable is a range of ratios of ethylene oxide to such C3 or higher alkylene oxides of from about 1:1.4 to about 1:4; more preferably from about 1:1.4 to about 1:3; and most preferably from about 1:1.4 to about 1:2; with, as noted above, propylene oxide the most preferred C3 or higher alkylene oxide monomer present therein.
  • Thus, the determination of a proper toner component for this purpose is rather difficult; triphenylmethanes are highly prevalent within the coloring industry as providing the desired range of color in terms of {circle over (2)}[0018] max absorption measurements. However, again, use of such a chromophore has compatibility concerns and problems. In addition, the selection of a proper toner in terms of solvent solubility as well as proper colorimetric values (e.g., CIELAB measurements for a*, b*, h*, and L*, as discussed in greater detail below) in order to provide the desire jet black, low redness, and low bronzing effects within the target drawn down ink has been reduced to the aforementioned polymeric colorants. In particular, it has been found that polymeric colorants such as MILLIJET® Violet X80 (an azo-based polymeric colorant, available from Milliken & Company) and other like nonionic chromophore-based polymeric colorants exhibiting {circle over (2)}max absorption measurements between the necessary wavelengths as noted above, are proper for this invention. Without being bound to any specific scientific theory, it is believed that such types of polymeric colorants provide the desired effects due to the proper violet or blue hue needed to eliminate or reduce the undesired brown undertone by altering the shade to lower b* values (less blue) as well as the superior compatibility due to the nonionic nature of the chromophore further enhanced and the resultant solvent solubility provided by the presence of such polyoxyalkylene chains.
  • Such gravure inks typically comprise (all in terms of weight percent within the total formulation) from 4-12% of a pigment and/or dyestuff (most prevalently carbon black or furnace black), from 0-8% of an extender pigment (such as alumina, calcium carbonate, and china clay), from 10 to 30% of a resin component (such as, most commonly modified resins, such as cellulose, polyamides, acrylic, vinyl, and/or hydrocarbon soluble resins), from 40 to 60% of a solvent (such as, most commonly toluene, while others, such as ketones, like methyl ethyl ketone, alcohols, like isopropyl alcohol, and esters, like ethyl acetate, as examples), and other additives, such as plasticizers, waxes and other types of like components, in amounts of from 2 to 10%. [0019]
  • The amount of toner component present within the inventive ink is from 0.01 to 50 parts per 100 parts of the total composition. Preferably, this amount is from 1 to 20 parts, more preferably from 2 to 15 parts, and most preferably from about 5 to about 10 parts. Surprisingly, it has been realized that higher concentrations (5 parts and higher, more particularly, above 6 parts) provide vast, unexpected improvements in measured hue angle and blueness of the sample inventive ink compositions. As noted below in greater detail, the blueness and corresponding hue angle are desirous and are surprisingly attained through the utilization of the inventive or otherwise selected toner components. [0020]
  • Of great importance to this invention, as well as any ink composition, is the ability for such a composition to provide desirable color, in terms of hue as well as visual effect. Visual color perception is based not in terms of red/green, yellow/blue, or other grouping of colors, but in terms of saturation (otherwise known as chroma) and hue. A numerical system of color differences is calculated in terms that agree with actual visual perception. Thus, to properly define or designate a particular label to a viewed color sample through analysis in a manner other than empirically, a measurement must be made of the distances between a sample color and a standard in the same values. Chroma is the amount of pure color contained in the sample, and is graphically measured (in CIELAB and/or CMC terms) as the distance from the center of the a* and b* axis for the sample. Brightness is a measurement of such a value for the particular sample of color. Hue angle is a measurement in terms of chroma as it is perceived by the viewer. A color difference between two distinct point on the axis can thus be described as the difference in each points' brightness (L*) value, the difference in their chroma (c*) value, and the difference in their hue angle (h*). Hue is measured in degrees from 0 to 360 (or a correlated negative angle on a Cartesian graph), where red is represented at the 0 angle, yellow at 90, green at 270 (or −90, for example), and blue at 360. The hue attribute of visual sensation has given rise to the color names (e.g., blue, green, yellow, red, etc.). Hue differences then depend primarily on variations in the wavelength of light reaching the eye at a particular angle from the viewed sample. Such a measurement (hue angle) is thus one of the three standard elements of color appearance (with the other two being brightness and saturation, or chroma, as noted above). Its colorimetric equivalent is dominant wavelength and, in terms of this invention, is of utmost importance, particularly for black offset inks, in providing a more effective, jetter, less red, less bronze, black ink. The target of this invention is thus to provide a hue angle closer to that of a typical blue measurement within the inventive ink after being drawn down on a surface. A hue angle measurement closer to the blue angle, or alternatively, further from the typical red angle, is thus the unexpected beneficial characteristic of these inventive inks, particularly as compared with the inks of the prior art comprising the state of the art in toning components (alkali blue pigment 61, etc., as discussed above).[0021]
  • DESCRIPTION OF THE PREFERRED EMBODIMENT
  • Without limiting the scope of the invention, the preferred features of the invention are hereinafter set forth. [0022]
  • EXAMPLE 1 Toluene-Based Inks
  • 15 parts of a polymeric violet colorant, oxirane, methyl-, polymer with oxirane, ether (ethoxylated ˜2-10 moles, propoxylated ˜4-14 moles) with 2,2′-((3-methyl-4->(2-amino-4-methyl-3,5-dicyanothiophene)azo-phenyl-imino-bis>ethanol (2:1), having a Color Value of 28, were mixed with 280 parts of Coated varnish (Resin No. 0180285) from Flint Ink, and 120 parts of toluene. The product was completely compatible. The final mixture was used as an ink and drawn down on paper. The image on paper is a brilliant violet and indicated that the individual components of the ink were completely compatible. [0023]
  • EXAMPLE 2 Toluene-Based Inks
  • 15 parts of the same polymeric violet colorant from EXAMPLE 1 were mixed with 280 parts of Coated varnish (Resin No 0180285) from Flint Ink, 120 parts of Toluene and 285 parts of a Black Concentrate (Flint Ink No 8040460). The product was allowed to mixed well and then drawn down on paper using a blade. The image was observed visually and measurements of l,a,b,c,h taken through analysis with an UltraScan® XE spectrophotometer (from HunterLab). The image empicially appears to be a jetter black. [0024]
  • EXAMPLE 3 Comparative Example
  • 15 parts of the Alkali Blue flush FB4365 from CPS Inc. was mixed with 280 parts of Coated varnish (Resin No 0180285) from Flint Ink, 120 parts of Toluene and 285 parts of a Black Concentrate (Flint Ink No 8040460). The product was allowed to mix well and then drawn down on paper using a blade. The image was observed visually and measurements of l,a,b,c,h taken. The image empirically appears to be a redder black as compared with EXAMPLE 2, above. [0025]
  • EXAMPLE 4 Comparative Example
  • 15 parts of Ink Blue 452 from Milliken Chemical was mixed with 280 parts of Coated varnish (Resin No 0180285) from Flint Ink, 120 parts of Toluene and 285 parts of a Black Concentrate (Flint Ink No 8040460). The product was allowed to mix well and then drawn down on paper using a blade. The image was observed visually and measurements of l,a,b,c,h taken. The image empirically appears to be a redder black as compared with EXAMPLE 2, above. [0026]
    TABLE
    Chromatic Properties of Inventive and Comparative Examples
    # Chromophore Loading L A B C h
    1 Control - untoned 0% 26.48 0.43 0.73 0.85 59.41
    2 (Example #3) 5% 27.35 0.99 0.97 1.39 44.48
    3 (Example #4) 5% 27.14 0.81 0.77 1.12 43.27
    4 (Example #2) 5% 26.38 1.12 0.70 1.32 31.86
  • Thus, the inventive inks exhibited vastly improved and unexpectedly good measurements, particularly for hue angle, as compared with the standard alkali blue-containing inks. [0027]
  • There are, of course, many alternate embodiments and modifications of the present invention which are intended to be included within the spirit and scope of the following claims. [0028]

Claims (10)

What I claim is:
1. A black gravure ink solution comprising at least one polymeric colorant toner component exhibiting a λmax absorption measurement between about 550 and 610 nm and comprising a nonionic chromophore component, at least one black coloring component selected from the group consisting of at least one black pigment, at least one black dyestuff, and a mixture of both, at least one solvent, and at least one resin component.
2. The black gravure ink solution of claim 1 wherein said solvent is toluene and said polymeric colorant toner component exhibits a λmax absorption measurement between about 560 and 580 nm.
3. The black gravure ink solution of claim 1 wherein said polymeric colorant toner component comprises polyoxyalkylene chains thereon.
4. The black gravure ink solution of claim 3 wherein said polyoxyalkylene chains comprise at least a majority of C3 or higher alkylene oxide monomers.
5. The black gravure ink solution of claim 4 wherein said polyoxyalkylene chains comprise a combination of ethylene oxide monomers and C3 or higher alkylene oxide monomers in a ratio of from about 1:1.4 to about 1:4.
6. The black gravure ink solution of claim 5 wherein said C3 or higher alkylene oxide monomer is propylene oxide.
7. The black gravure ink solution of claim 2 wherein said polymeric colorant toner component comprises polyoxyalkylene chains thereon.
8. The black gravure ink solution of claim 7 wherein said polyoxyalkylene chains comprise at least a majority of C3 or higher alkylene oxide monomers.
9. The black gravure ink solution of claim 8 wherein said polyoxyalkylene chains comprise a combination of ethylene oxide monomers and C3 or higher alkylene oxide monomers in a ratio of from about 1:1.4 to about 1:4.
10. The black gravure ink solution of claim 9 wherein said C3 or higher alkylene oxide monomer is propylene oxide.
US10/749,446 2001-10-26 2003-12-31 Novel toner compositions for black gravure inks Abandoned US20040167250A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US10/749,446 US20040167250A1 (en) 2001-10-26 2003-12-31 Novel toner compositions for black gravure inks

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/001,347 US6737450B2 (en) 2001-10-26 2001-10-26 Toner compositions for black gravure inks
US10/749,446 US20040167250A1 (en) 2001-10-26 2003-12-31 Novel toner compositions for black gravure inks

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US10/001,347 Continuation US6737450B2 (en) 2001-10-26 2001-10-26 Toner compositions for black gravure inks

Publications (1)

Publication Number Publication Date
US20040167250A1 true US20040167250A1 (en) 2004-08-26

Family

ID=21695578

Family Applications (3)

Application Number Title Priority Date Filing Date
US10/001,347 Expired - Fee Related US6737450B2 (en) 2001-10-26 2001-10-26 Toner compositions for black gravure inks
US10/678,716 Expired - Fee Related US6894087B2 (en) 2001-10-26 2003-10-03 Toner compositions for black gravure inks
US10/749,446 Abandoned US20040167250A1 (en) 2001-10-26 2003-12-31 Novel toner compositions for black gravure inks

Family Applications Before (2)

Application Number Title Priority Date Filing Date
US10/001,347 Expired - Fee Related US6737450B2 (en) 2001-10-26 2001-10-26 Toner compositions for black gravure inks
US10/678,716 Expired - Fee Related US6894087B2 (en) 2001-10-26 2003-10-03 Toner compositions for black gravure inks

Country Status (1)

Country Link
US (3) US6737450B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060160009A1 (en) * 2005-01-18 2006-07-20 Itipon Padunchwit Color toner and developer compositions and processes for making and using such compositions
CN111205716A (en) * 2020-02-28 2020-05-29 深圳市冠为科技股份有限公司 UV gloss oil capable of gold stamping and preparation method and application thereof

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7776108B2 (en) 2005-06-07 2010-08-17 S.C. Johnson & Son, Inc. Composition for application to a surface
US20070277849A1 (en) 2006-06-06 2007-12-06 Shah Ketan N Method of neutralizing a stain on a surface
AU2006255106A1 (en) 2005-06-07 2006-12-14 S. C. Johnson & Son, Inc. Composition for application to a surface
US7642282B2 (en) * 2007-01-19 2010-01-05 Milliken & Company Whitening agents for cellulosic substrates
US20080177089A1 (en) 2007-01-19 2008-07-24 Eugene Steven Sadlowski Novel whitening agents for cellulosic substrates
US8715368B2 (en) 2010-11-12 2014-05-06 The Procter & Gamble Company Thiophene azo dyes and laundry care compositions containing the same
US9163146B2 (en) 2011-06-03 2015-10-20 Milliken & Company Thiophene azo carboxylate dyes and laundry care compositions containing the same
CN104774491A (en) * 2015-03-28 2015-07-15 安徽美翔塑业有限公司 Gravure printing compound ink
KR20170038398A (en) 2015-09-30 2017-04-07 주식회사 쇼앤리 system and method for managing service to pay rent

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4284729A (en) * 1980-03-31 1981-08-18 Milliken Research Corporation Process for coloring thermosetting resins
US4812141A (en) * 1985-09-13 1989-03-14 Milliken Research Corporation Colored thermoplastic resin composition
US5194463A (en) * 1991-09-27 1993-03-16 Eastman Kodak Company Light-absorbing polyurethane compositions and thermoplastic polymers colored therewith
US5429841A (en) * 1993-06-25 1995-07-04 Milliken Research Corporation Printing ink emulsion with poly(oxyalkylene) substituted colorant
US5886091A (en) * 1996-01-05 1999-03-23 Milliken & Company Printing ink composition
US5955523A (en) * 1997-11-07 1999-09-21 Milliken Research Corporation Polyoxalkylenated disazo colored thermoplastic resins
US6299941B1 (en) * 1997-07-31 2001-10-09 Xerox Corporation Process of painting with inks with colored resin emulsion particles
US6369128B1 (en) * 1997-02-07 2002-04-09 Milliken & Company Aqueous ink composition
US6566425B1 (en) * 2001-09-18 2003-05-20 Milliken & Company Polymeric articles comprising novel bismethine benzodifuranone derivative colorants
US20030127023A1 (en) * 1999-07-09 2003-07-10 Yves Grandidier Pigments having improved colouristic properties and process for their preparation
US6632858B1 (en) * 1998-03-31 2003-10-14 Avecia Limited Colored polyurethanes
US20040192797A1 (en) * 2003-03-27 2004-09-30 Jusong Xia High-strength black polyurethane foams

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4032357A (en) * 1976-03-03 1977-06-28 The Sherwin-Williams Company Easy dispersing alkali blue powder and process for manufacture
US4373962A (en) * 1981-06-08 1983-02-15 Basf Wyandotte Corporation Surface treated alkali blue pigment
US4383865A (en) * 1981-06-08 1983-05-17 Basf Wyandotte Corporation Soft textured high strength alkali blue pigment
US5026627A (en) * 1988-10-14 1991-06-25 Basf Corporation High strength alkali blue pigment toner useful in both oil-based and water-based systems
US5176745A (en) * 1991-12-11 1993-01-05 Milliken Research Corporation Aqueous ink composition and colorants useful therein
DE4335540A1 (en) * 1993-10-19 1995-04-20 Basf Ag Azo dye groups and polyadduct containing urethane groups and their use in non-linear optics
US5637638A (en) 1995-08-24 1997-06-10 Bic Corporation Erasable ink composition containing a waterborne polyurethane-urea derived from an aromatic amine dye monomer and marking instrument containing same
GB2305670A (en) 1995-09-27 1997-04-16 Coates Brothers Plc Hot melt ink jet vehicles
US5700851A (en) 1995-10-17 1997-12-23 Tektronix, Inc. Ink-jet ink composition containing a colored polyurethane dispersion
US5782966A (en) 1996-06-28 1998-07-21 Tektronix, Inc. Isocyanate-derived materials for use in phase change ink jet inks
MXPA03002614A (en) * 2000-09-29 2003-06-19 Milliken Company Inks exhibiting expanded color-space characteristics for water-based printing.

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4284729A (en) * 1980-03-31 1981-08-18 Milliken Research Corporation Process for coloring thermosetting resins
US4812141A (en) * 1985-09-13 1989-03-14 Milliken Research Corporation Colored thermoplastic resin composition
US5194463A (en) * 1991-09-27 1993-03-16 Eastman Kodak Company Light-absorbing polyurethane compositions and thermoplastic polymers colored therewith
US5194463B1 (en) * 1991-09-27 1995-06-20 Eastman Kodak Co Light-absorbing polyurethane compositions and thermoplastic polymers colored therewith
US5429841A (en) * 1993-06-25 1995-07-04 Milliken Research Corporation Printing ink emulsion with poly(oxyalkylene) substituted colorant
US5886091A (en) * 1996-01-05 1999-03-23 Milliken & Company Printing ink composition
US6369128B1 (en) * 1997-02-07 2002-04-09 Milliken & Company Aqueous ink composition
US6299941B1 (en) * 1997-07-31 2001-10-09 Xerox Corporation Process of painting with inks with colored resin emulsion particles
US5955523A (en) * 1997-11-07 1999-09-21 Milliken Research Corporation Polyoxalkylenated disazo colored thermoplastic resins
US6632858B1 (en) * 1998-03-31 2003-10-14 Avecia Limited Colored polyurethanes
US20030127023A1 (en) * 1999-07-09 2003-07-10 Yves Grandidier Pigments having improved colouristic properties and process for their preparation
US6566425B1 (en) * 2001-09-18 2003-05-20 Milliken & Company Polymeric articles comprising novel bismethine benzodifuranone derivative colorants
US20040192797A1 (en) * 2003-03-27 2004-09-30 Jusong Xia High-strength black polyurethane foams

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060160009A1 (en) * 2005-01-18 2006-07-20 Itipon Padunchwit Color toner and developer compositions and processes for making and using such compositions
WO2006078616A1 (en) * 2005-01-18 2006-07-27 Milliken & Company Color toner and developer compositions and processes for making and using such compositions
US7399566B2 (en) 2005-01-18 2008-07-15 Milliken & Company Color toner and developer compositions and processes for making and using such compositions
CN100561362C (en) * 2005-01-18 2009-11-18 美利肯公司 The method of manufacture and use thereof of color toner and developer composition and said composition
CN111205716A (en) * 2020-02-28 2020-05-29 深圳市冠为科技股份有限公司 UV gloss oil capable of gold stamping and preparation method and application thereof

Also Published As

Publication number Publication date
US20030082349A1 (en) 2003-05-01
US20040068032A1 (en) 2004-04-08
US6737450B2 (en) 2004-05-18
US6894087B2 (en) 2005-05-17

Similar Documents

Publication Publication Date Title
US6794426B2 (en) Toner compounds and compositions for black offset inks
US6610131B2 (en) Inks exhibiting expanded color-space characteristics for water-based printing
US6001168A (en) Pigment dispersions comprising C.I. Pigment Red 222
TW583280B (en) Waterborne colorant preparations for ink jet printing
US6737450B2 (en) Toner compositions for black gravure inks
US11773267B2 (en) Method for producing quinacridone solid solution pigment, pigment dispersion, and inkjet ink
CN102585598A (en) Oil ink set
JP5035718B2 (en) Pigment dispersant and use thereof
US7255737B2 (en) Organic formulations of pigment
EP1217047A2 (en) Pigmented aqueous inks and ink set for ink jet printers
US6793722B2 (en) Inkjet ink composition with high chroma
CN111902490A (en) Process for producing quinacridone solid solution pigment, pigment dispersion liquid, and ink-jet ink
GB2370580A (en) Ink for Ink Jet Printers
US6710102B2 (en) Toned black offset inks exhibiting excellent chromatic characteristics
JP4786013B2 (en) Polychromatic powder and polychromatic coating
JP2000191935A (en) Insoluble azo pigment compound and use thereof
JP3116640B2 (en) Blue pigment composition
JP2000186241A (en) Magenta ink for ink jet and its preparation
US20050143487A1 (en) Aqueous flexographic printing inks
CN115894782A (en) High-temperature direct-injection dispersing color paste and preparation method and application thereof
US7022409B2 (en) Pleochroism powder and pleochroism printed article
KR20200087675A (en) Azo pigment composition and manufacturing method thereof
MXPA06007580A (en) Aqueous flexographic printing inks
WO2003037951A1 (en) Novel toner compounds and compositions for black offset inks

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION