US3054751A - Magnetic lithographic inks - Google Patents

Magnetic lithographic inks Download PDF

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Publication number
US3054751A
US3054751A US783997A US78399758A US3054751A US 3054751 A US3054751 A US 3054751A US 783997 A US783997 A US 783997A US 78399758 A US78399758 A US 78399758A US 3054751 A US3054751 A US 3054751A
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ink
pigment
magnetic
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particles
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US783997A
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Carl B Blake
Lewis F Miller
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International Business Machines Corp
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International Business Machines Corp
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Priority to CH8237159A priority patent/CH397735A/en
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F41/00—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
    • H01F41/14—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates
    • H01F41/16—Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates the magnetic material being applied in the form of particles, e.g. by serigraphy, to form thick magnetic films or precursors therefor
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/26—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
    • C04B35/265—Compositions containing one or more ferrites of the group comprising manganese or zinc and one or more ferrites of the group comprising nickel, copper or cobalt
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/006—Combinations of treatments provided for in groups C09C3/04 - C09C3/12
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/08—Treatment with low-molecular-weight non-polymer organic compounds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
    • C09C3/10—Treatment with macromolecular organic compounds
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/60—Particles characterised by their size
    • C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/12—Surface area
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/90—Other properties not specified above

Definitions

  • This invention relates to magnetic lithographic inks and more particularly to oleophilic lithographic inks containing hydrophilic magnetic pigments.
  • Lithographic printing is well known in the art and generally involves the use of a plate having a portion of its surface treated so as to be wetted by a solution which is essentially water, and having the remainder of its surface treated to resist wetting by the solution and to be wetted by an oleophilic ink.
  • the solution is applied to the plate by such applicators as, for example rollers carrying a film of the solution.
  • the plate subsequently contacts an ink laden roller. Ink on the roller is repelled by the water-bearing areas of the plate and accepted by non-water bearing areas thereof.
  • the ink image is subsequently transferred to a work surface which prints the image on a desired sub-strate, such as, for example, a sheet of paper.
  • a desired sub-strate such as, for example, a sheet of paper.
  • Many compositions of suitable inks and fountain solutions are well known in the lithographic printing arts and have been employed for many years.
  • Magnetic inks employ magnetic pigments in powder form. It is essential that a high pigment loading is provided in the ink in order that suitable signal strength will be obtained when the printed characters are sensed by magnetic sensing means. These high pigment loadings of magnetic pigments increase the emulsification tendencies of the ink. This increase results, in substantial part, from the hydrophilicity of magnetic pigment particles. Thus there tends to form, on the ink applying roller of the lithographic press, an emulsification of water picked up from the water wet surface of the plate. This emulsion adversely effects the printing operation, producing a deposition of magnetic ink particles on the water wet plate and a deposition of water particles on the ink receiving areas of the plate. Not only does this produce bad printing and spotty work but also the magnetic characteristics of the printed areas are lowered, adversely affecting subsequent magnet sensing operation.
  • a further object of the invention is to provide better wetting of the pigment particles by the varnishes which latitude in the use of fountain solutions.
  • lithographic inks are contained in lithographic inks to provide better rheological properties of the ink, better printing coverage by the ink, and darker or deeper appearance of the printed ink.
  • a further object of the invention is to provide wider Such latitude is particularly desirable when paper masters or plates are employed. Paper masters are specifically treated and require the use of special fountain solutions which may adversely affect inks and have greater tendencies than other fountain solutions to emulsify with inks.
  • a further object of the invention is to provide a 1itho grahic ink employing magnetic pigments of desirable magnetic properties wherein undesirable coloration properties of the pigment are overcome simultaneously with a reduction in hydrophilicity of the magnetic pigment particles.
  • magnétique pigments will be employed to refer to any of numerous well known magnetic pigments suitable for use in magnetic inks.
  • Such pigments include, for example: gamma ferric oxide with remanences of 1,500 gausses or more, coercivities of between 200 and 400 oerste-ds, and particle size range of 1-10 microns; natural or artificial magnetites of similar properties; unicrystalline iron of similar properties; small particle magnetic alloys; and cobalt, nickel and barium ferrites and similar materials.
  • One general form of treatment which may be employed for reducing the emulsification tendencies of magnetic pigments, such as those listed above, is to coat the pigment particles with a suitable resin.
  • resins may, for example, include: silicones, vinyl acetates, chlorides, polyethylenes, polyamides, phenolics, alkyds, cournaroneindene, and epoxy resins.
  • One method of accomplishing resin coating of pigment particles is by providing the resin in fluid form, such as in a molten state, and stirring the pigment into the resin. Thereafter the resin is cooled and crushed, and the pigment particles are then recovered in coated form.
  • Another fluid coating method involves the use of heated two roller mill dispersion of a pigment in a resin, followed by cooling and chip crushing.
  • Another method which may be employed for coating the pigment particles with a resin involves the deposition of the resin from a solution onto the pigment particles. This may be done, for example, by fractionation or by pigment seeding techniques.
  • pigment seeding pigment particles are added to a supersaturated solution of a resin in a solvent while the resin is precipitated by cooling or by digestion. Precipitated resin will accumulate on the pigment particles and coat each of the particles.
  • fractionation processes the resin is dissolved in a solvent, pigment is then stirred into the solution and while stirring a poor solvent is added to the solution-throwing the resin out of solution. The resin coming out of solution coats the pigment particles thinly and evenly.
  • Resin Good Solvent i Poor Solvent 1 I 1 vinyl chloride tetrahydrofuran' benzene. 2 chlorinated paraffin. nitrobenzene methylalcohol. 3 rain ethanol water.
  • the amount of resin precipitated should be equal to the oil absorption of the pigment, i.e., the amount of resin precipitated should be sufficient to cover all of the powder surface.
  • a second general form of treatment which may be employed for reducing the emulsification tendencies of pigments, such as those listed above, is to coat the pigments with dye surfactants by laking procedures.
  • dyestuffs in the form of molecular chains having one end portions of hydrophilic nature and the other end portion of oleophilic nature.
  • Various well known dyestuffs may be employed and upon application to magnetic pigment particles, attach to the particle by their hydrophilic portion leaving their oleophilic portion extending outwardly from the pigment particles and presenting hydrophobic surfaces to any water particles which may be encountered.
  • Example 1 The following materials are mixed to form a slurry:
  • red colorant as red lake 7013.
  • a third general form of treatment which may be eni-i ployed for reducing the emulsification tendencies of ma netic pigments such as those listed above, is to treat the pigment with chemically reactive materials giving rise to phosphatizing, nitrating and other surface reactions on the pigment particles which will provide roughened pigment particle surfaces and improved pigment particle hydrophobicity. Such treatments will result in improved wetting of pigment particles by the resins in an ink formulation. Such processes are well known in the art and need not be described in detail herein.
  • Viscosity Z 5 /2 at 77 F.
  • black colorant consisting of 20 parts impingement black, particle size 24 millimicrons, flushed into #0 and #3 bodied linseed oils.
  • a fourth general form of treatment which may be employed for reducing the emulsification tendencies of magnetic pigments involves mixing the pigments with suitable surface active agents.
  • suitable surface active agents such as those set forth in the following examples may be either mixed directly with the dry magnetic pigment or, preferably may be dissolved in a solvent into which the magnetic pigments are stirred, whereupon the solvents are evaporated off, leaving the pigment particles coated with the surface active agent.
  • the use of the solvent coating technique provides improved uni-formity of coating.
  • Certain surface active agents are then desirably treated to improve their effectiveness in reducing the hydrophilicity of the pigment particles.
  • Example 1 5% by Weight ricinoleic acid mixed with 95% by weight of a ferric iron oxide magnetic pigment such as IRN-100. While the ricinoleic acid is preferably mixed with a solvent such as heptane B, the mix may be made in dry powder form. After the materials are tho-roughly mixed and, if solvent is used, the solvent driven off, the coated magnetic particles are employed as pigment in a suitable magnetic ink formulation such as numerous formulations well known in the art.
  • a suitable magnetic ink formulation such as numerous formulations well known in the art.
  • a ferric. oxide such as IRN-10O
  • surface active agents which may be employed are: organic aluminum compounds, oil soluble non-ionic ammonium surfactants, and other applicable anionic and cationic surfactants.
  • i'Following is an example of an ink formulation embodying pigment particles treated by the fourth form of treattfnent described above:
  • black colorant base consisting of 20 parts by Weight of impingement carbon black, particle size 24 millimicrons, flushed into #0 and #3 bodied linseed oil.
  • An oleophilic lithographic ink consisting essentially of a minor proportion of an oleophilic ink vehicle and a major proportion of a magnetizable hydrophobic pigment, said pigment consisting of normally hydrophilic magnetizable particles having a largest dimension of 10 microns or less and a relatively thin coating deposited on said particles, said coating having an external surface which is substantially hydrophobic and wettable by said vehicle whereby a magnetizable water-repelling ink is provided.
  • a surface active agent selected from the class consisting of ricinoleic acid, organic aluminum compounds, oil soluble non-ionic ammonium surfactants and the reaction product of a mixture of di-alkyl quaternary ammonium chloride and an ethoxy-lated amine acetate with sodium hydroxide.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Power Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Description

Patented Sept. 18, 1962 fire 3,054,751 MAGNETIC LKTHOGRAPEHC INKS Carl B. Blake, Great Neck, and Lewis F. Miller, New
Paitz, N.Y., assignors to international Business Machines Corporation, New York, N.Y., a corporation of New York No Drawing. Filed Dec. 30, 1958, Ser. No. 783,997 5 Claims. (Cl. 252-625) This invention relates to magnetic lithographic inks and more particularly to oleophilic lithographic inks containing hydrophilic magnetic pigments.
Lithographic printing is well known in the art and generally involves the use of a plate having a portion of its surface treated so as to be wetted by a solution which is essentially water, and having the remainder of its surface treated to resist wetting by the solution and to be wetted by an oleophilic ink. The solution is applied to the plate by such applicators as, for example rollers carrying a film of the solution. The plate subsequently contacts an ink laden roller. Ink on the roller is repelled by the water-bearing areas of the plate and accepted by non-water bearing areas thereof. The ink image is subsequently transferred to a work surface which prints the image on a desired sub-strate, such as, for example, a sheet of paper. Many compositions of suitable inks and fountain solutions are well known in the lithographic printing arts and have been employed for many years.
With recent developments of automation in accounting there have been developed devices for identifying characters printed with magnetic inks and, in certain applications, it is highly desirable to employ the lithographic printing process for depositing these inks.
Magnetic inks employ magnetic pigments in powder form. It is essential that a high pigment loading is provided in the ink in order that suitable signal strength will be obtained when the printed characters are sensed by magnetic sensing means. These high pigment loadings of magnetic pigments increase the emulsification tendencies of the ink. This increase results, in substantial part, from the hydrophilicity of magnetic pigment particles. Thus there tends to form, on the ink applying roller of the lithographic press, an emulsification of water picked up from the water wet surface of the plate. This emulsion adversely effects the printing operation, producing a deposition of magnetic ink particles on the water wet plate and a deposition of water particles on the ink receiving areas of the plate. Not only does this produce bad printing and spotty work but also the magnetic characteristics of the printed areas are lowered, adversely affecting subsequent magnet sensing operation.
It is the primary object of this invention to provide a lithographic ink containing a magnetic pigment treated to present hydrophobic surfaces for reducing emulsification tendencies of the ink.
More specifically, it is among the objects of the invention to reduce emulsification tendencies of the lithographic ink containing a magnetic pigment in order to provide better magnetic properties of characters printed thereby, better drying of the printed ink due to minimization of the water content thereof, darker and better appearance of the printed ink due to the minimization of water content thereof, a wider latitude in press control, i.e. in the control of the application of the fountain solution and the ink, thus simplifying press control and the capacity for long run operation with fountain solutions previously not usable.
A further object of the invention is to provide better wetting of the pigment particles by the varnishes which latitude in the use of fountain solutions.
are contained in lithographic inks to provide better rheological properties of the ink, better printing coverage by the ink, and darker or deeper appearance of the printed ink.
A further object of the invention is to provide wider Such latitude is particularly desirable when paper masters or plates are employed. Paper masters are specifically treated and require the use of special fountain solutions which may adversely affect inks and have greater tendencies than other fountain solutions to emulsify with inks.
A further object of the invention is to provide a 1itho grahic ink employing magnetic pigments of desirable magnetic properties wherein undesirable coloration properties of the pigment are overcome simultaneously with a reduction in hydrophilicity of the magnetic pigment particles.
These and other objects of the invention are accomplished primarily by a lithographic ink containing magnetic pigments in which the pigment particles are treated to present hydrophobic surfaces.
Hereafter the term magnetic pigments will be employed to refer to any of numerous well known magnetic pigments suitable for use in magnetic inks. Such pigments include, for example: gamma ferric oxide with remanences of 1,500 gausses or more, coercivities of between 200 and 400 oerste-ds, and particle size range of 1-10 microns; natural or artificial magnetites of similar properties; unicrystalline iron of similar properties; small particle magnetic alloys; and cobalt, nickel and barium ferrites and similar materials.
One general form of treatment which may be employed for reducing the emulsification tendencies of magnetic pigments, such as those listed above, is to coat the pigment particles with a suitable resin. Such resins may, for example, include: silicones, vinyl acetates, chlorides, polyethylenes, polyamides, phenolics, alkyds, cournaroneindene, and epoxy resins.
One method of accomplishing resin coating of pigment particles is by providing the resin in fluid form, such as in a molten state, and stirring the pigment into the resin. Thereafter the resin is cooled and crushed, and the pigment particles are then recovered in coated form. Another fluid coating method involves the use of heated two roller mill dispersion of a pigment in a resin, followed by cooling and chip crushing.
Another method which may be employed for coating the pigment particles with a resin involves the deposition of the resin from a solution onto the pigment particles. This may be done, for example, by fractionation or by pigment seeding techniques. In pigment seeding, pigment particles are added to a supersaturated solution of a resin in a solvent while the resin is precipitated by cooling or by digestion. Precipitated resin will accumulate on the pigment particles and coat each of the particles. In fractionation processes the resin is dissolved in a solvent, pigment is then stirred into the solution and while stirring a poor solvent is added to the solution-throwing the resin out of solution. The resin coming out of solution coats the pigment particles thinly and evenly.
Following are examples of resins and solvents which may be employed in seeding techniques.
a, :3 Following are examples of resins and solvents which may be employed in fractionation techniques.
Resin Good Solvent i Poor Solvent 1 I 1 vinyl chloride tetrahydrofuran' benzene. 2 chlorinated paraffin. nitrobenzene methylalcohol. 3 rain ethanol water.
In the foregoing precipitation coating methods the amount of resin precipitated should be equal to the oil absorption of the pigment, i.e., the amount of resin precipitated should be sufficient to cover all of the powder surface.
Following is an example of an ink formulation embody ing pigment particles treated by the general form of treatment described above:
A second general form of treatment which may be employed for reducing the emulsification tendencies of pigments, such as those listed above, is to coat the pigments with dye surfactants by laking procedures.
Well known laking procedures involve the use of dyestuffs in the form of molecular chains having one end portions of hydrophilic nature and the other end portion of oleophilic nature. Various well known dyestuffs may be employed and upon application to magnetic pigment particles, attach to the particle by their hydrophilic portion leaving their oleophilic portion extending outwardly from the pigment particles and presenting hydrophobic surfaces to any water particles which may be encountered.
Following are examples of laking procedures which may be employed:
Example 1 The following materials are mixed to form a slurry:
Gms. Water (hot) 30,000 Acetic acid, 56% 100 Rhodamine 6 GDN 500 Heat to 90 C.; stir until dissolved. Add: Densed carbonyl iron oxide regular 1,055
The following materials are mixed to form a solution:
Gms. Water (hot) r 6,000 Sodium tungstate, cryst 995 60 Sodium molybdate, cryst 95 Di-sodium phosphate 115 20 Baum muriatic acid 800 55 gms. ferric oxide, gamma crystalline form, obtained by oxidation of pure iron globules created by decomposition of carbonyl iron, said globules to be under 10 microns in diameter. Resulting ferric oxide is densed, to lower oil absorption, then laked with rhodamine tungstate-molybdate (described above).
5 gms. red colorant, as red lake 7013.
16 gms. solids isophthalic alkyd varnish, viscosity Z 2% Gardner tube at 77 F.
15 gms. varnish, consisting of 50 parts rosin modified phenol formaldehyde resin, melting point 127133 C. in petroleum solvent, boiling point 590 F. Viscosity: Z 6% at 77 F. Gardner tube.
4 gms. petroleum solvent, boiling point 535 F.
2 gms. 21% cobalt drier. p
3 gms. proprietary wetting agent, such as for example: Tenlo 70, manufactured by Nopco Chemical Company.
A third general form of treatment which may be eni-i ployed for reducing the emulsification tendencies of ma netic pigments such as those listed above, is to treat the pigment with chemically reactive materials giving rise to phosphatizing, nitrating and other surface reactions on the pigment particles which will provide roughened pigment particle surfaces and improved pigment particle hydrophobicity. Such treatments will result in improved wetting of pigment particles by the resins in an ink formulation. Such processes are well known in the art and need not be described in detail herein.
Following is an example of an ink formulation embodying pigment particles treated by the third form of treatment described above:
68 gms. phosphatized natural magnetite, reduced in particle size to under 5 microns average.
10 gms. bodied China-wood oil, Gardner bubble tube.
Viscosity: Z 5 /2 at 77 F.
9 gms. 100% solids isophthalic alkyd varnish, Gardner bubble tube viscosity Z 2% at 70 F.
8 gms. black colorant, consisting of 20 parts impingement black, particle size 24 millimicrons, flushed into #0 and #3 bodied linseed oils.
2 gms. 21% cobalt drier.
3 gms. paraffin oil, light. Viscosity: 135.
A fourth general form of treatment which may be employed for reducing the emulsification tendencies of magnetic pigments, such as those listed above, involves mixing the pigments with suitable surface active agents. Suitable surface active agents such as those set forth in the following examples may be either mixed directly with the dry magnetic pigment or, preferably may be dissolved in a solvent into which the magnetic pigments are stirred, whereupon the solvents are evaporated off, leaving the pigment particles coated with the surface active agent. The use of the solvent coating technique provides improved uni-formity of coating. Certain surface active agents are then desirably treated to improve their effectiveness in reducing the hydrophilicity of the pigment particles. The following are examples of surface active agent treatments:
Example 1 5% by Weight ricinoleic acid mixed with 95% by weight of a ferric iron oxide magnetic pigment such as IRN-100. While the ricinoleic acid is preferably mixed with a solvent such as heptane B, the mix may be made in dry powder form. After the materials are tho-roughly mixed and, if solvent is used, the solvent driven off, the coated magnetic particles are employed as pigment in a suitable magnetic ink formulation such as numerous formulations well known in the art.
Example 2 3 grams of a surfactant comprising a 5 to 1 mixture of dialkyl quaternary ammonium chloride and an ethoxylated amine acetate is mixed with 97 grams of a ferric. oxide such as IRN-10O by first dissolving the surfactant in warm water and then adding the solution to a loose slurry of the iron oxide in Water. The resultant slurry is stirred for to minutes and then cc. of a 1% =NaOH solution is added to this slurry with continued stirring for an additional 15 minutes. There results a molecnlar interchange providing a strongly bonded coating on each pigment particle. Thereafter the slurry is filtered and the filtrate is washed and dried. The coated pigment filtrate may then be used in a conventional magnetic lithographic ink formulation.
Further examples of surface active agents which may be employed are: organic aluminum compounds, oil soluble non-ionic ammonium surfactants, and other applicable anionic and cationic surfactants.
i'Following is an example of an ink formulation embodying pigment particles treated by the fourth form of treattfnent described above:
i/SS gms. gamma ferric oxide particle size .3 x 2 microns average, exemplified by IRN-IOO pigment, coated with 5% ricinoleic acid, as described above.
17 gms. heavy body 100% solids isophthalic alkyd varnish, viscosity Z 7 /2 on Gardner tube.
10 gms. loose body 100% solids isophthalic alkyd varnish, viscosity Z 2%, at 77 F. on Gardner tube.
8 gms. black colorant base, consisting of 20 parts by Weight of impingement carbon black, particle size 24 millimicrons, flushed into #0 and #3 bodied linseed oil.
5 gms. blue toner, consisting of 41 parts by weight prussian alkali blue in linseed oil.
4 gms. paraflin oil, light. Viscosity: 125/135.
From the foregoing, it will be evident that various methods may be employed for treating magnetic pigment particles for reducing emulsification tendencies of lithographic ink brought about by the hydrophilicity of magnetic pigment particles. It will also be evident to one skilled in the art of compounding lithographic inks that magnetic pigment particles treated in accordance with the foregoing, may be employed in numerous ink formulations and that any given formulation will be dependent upon the conditions of lithographic printing that the ink must satisfy. For example, ink formulations are influenced by the nature of the printing plate, the nature and the work surface on which the printing is ultimately accomplished, the particular printing characteristics desired, i.e., sharpness, color depth, etc., and numerous other considerations well know to those skilled in the lithographic printing art. The invention disclosed herein, however, is applicable to a great variety of lithographic printing applications and it will be evident to one skilled in the art that the various methods by which the pigment particles may be coated may be selectively employed depending upon other considerations involved in the compounding of a particular ink for a particular purpose without departing from the scope of the invention as set forth in the following claims.
What is claimed is:
1. An oleophilic lithographic ink consisting essentially of a minor proportion of an oleophilic ink vehicle and a major proportion of a magnetizable hydrophobic pigment, said pigment consisting of normally hydrophilic magnetizable particles having a largest dimension of 10 microns or less and a relatively thin coating deposited on said particles, said coating having an external surface which is substantially hydrophobic and wettable by said vehicle whereby a magnetizable water-repelling ink is provided.
2. A lithographic ink as recited in claim 1 in which said coating is a resinous material selected from the class consisting of melamine resins, cyclized rubber, silicones, vinyl chloride, chlorinated paraflines and zein.
3. A lithographic ink as recited in claim 1 in which said coating is a dyestuif having a molecular chain with one end portion of a hydrophilic nature attached to said particle and the other end portion is of an oleophilic nature.
4. A lithographic ink as recited in claim 1 in which said coating is a surface active agent selected from the class consisting of ricinoleic acid, organic aluminum compounds, oil soluble non-ionic ammonium surfactants and the reaction product of a mixture of di-alkyl quaternary ammonium chloride and an ethoxy-lated amine acetate with sodium hydroxide.
5. An ink as recited in claim 3 in which said coating is a rhodamine tungstate-molybdate dye.
References Cited in the file of this patent UNITED STATES PATENTS 607,875 Peak July 26, 1898 1,960,899 De Forest May 29, 1934 2,232,352 Verweij et a1. Feb. 18, 1941 2,267,999 Switzer Dec. 30, 1941 2,346,968 Jeuck et a1. Apr. 18, 1944 2,346,969 Jeuck et al. Apr. 18, 1944 2,384,579 Vesee Sept. 11, 1945 2,559,505 Hiller July 3, 1951 2,601,212 Polydoroff June 17, 1952 2,684,909 Leekley et a1. July 27, 1954 2,688,649 Bjorksten Sept. 7, 1954 2,800,458 Green July 23, 1957 2,875,152 Van Scoy Feb. 214, 1959 2,920,042 Eastman Jan. 5, 1960 OTHER REFERENCES Wolfe: Printing and Litho Inks, 4th ed., pub. by Mac- Nair-Dorland Co. (1949), pp. 270-276.

Claims (1)

1. AN OLEOPHILIC LITHOGRAPHIC INK CONSISTING ESSENTIALLY OF A MINOR PROPORTION OF AN OLEPHILIC INK VEHICLE AND A MAJOR PROPORTION OF A MAGNETIZABLE HYDROPHOBIC PIGMENT, SAID PIGMENT CONSISTING OF NORMALLY HYDROPHILIC MAGNETIZABLE PARTICLES HAVING A LARGEST DIMENSION OF 10 MICORNS OF LESS AND A RELATIVELY THIN COATING DEPOSITED ON SAID PARTICLES, SAID COATING HAVING AN EXTERNAL SURFACE WHICH IS SUBSTANTIALLY HYDROPHOBIC AND WETTABLE BY SAID VEHICLE WHEREBY A MAGNETIZABLE WATER-REPELLING INK IS PROVIDED.
US783997A 1958-12-30 1958-12-30 Magnetic lithographic inks Expired - Lifetime US3054751A (en)

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CH8237159A CH397735A (en) 1958-12-30 1959-12-28 Magnetic Dye Particle Ink and Process for Making the Same - US Pat
GB44077/59A GB935541A (en) 1958-12-30 1959-12-29 Magnetic lithographic inks

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US3185589A (en) * 1961-12-21 1965-05-25 Ibm Method of coating finely divided metal particles
US3207622A (en) * 1962-03-05 1965-09-21 Standard Oil Co Method of producing hydrophobicorganophilic magnetic pigments
US3247117A (en) * 1960-05-06 1966-04-19 Dick Co Ab Magnetic lithographic ink
US3294686A (en) * 1966-12-27 Pigment particles coated with organo-alumtnum compounds
US3519452A (en) * 1967-03-09 1970-07-07 Cabot Corp Sulfonated carbon black pigmented compositions
US3547822A (en) * 1968-02-01 1970-12-15 Eastman Kodak Co Scum-retardant carrier particles and compositions thereof
US3905935A (en) * 1973-01-15 1975-09-16 Hercules Inc Dye laking resins for printing inks
US3929657A (en) * 1973-09-05 1975-12-30 Xerox Corp Stoichiometric ferrite carriers
US3947371A (en) * 1972-11-21 1976-03-30 Xerox Corporation Developer material with poly(p-xylylene) coated carrier
US4018601A (en) * 1969-06-19 1977-04-19 Xerox Corporation Electrostatographic magnetic brush imaging process employing carrier beads comprising high purity nickel
US4025690A (en) * 1970-07-06 1977-05-24 Reagens S.P.A. Industria Chimica Method of preparing additives and additives prepared according to said method
US4107063A (en) * 1977-03-02 1978-08-15 International Business Machines Corporation Water based selectable charge magnetic inks
US4285994A (en) * 1977-08-17 1981-08-25 Johnson, Matthey & Co., Limited Process for production of free flowing dust-free pigments
US5127952A (en) * 1986-10-10 1992-07-07 Rohne-Poulenc Chimie Core/oxide/dye pigmentary colorants
US20050046176A1 (en) * 2003-08-26 2005-03-03 Crum Jesse D. Communication substrates having variably applied ferromagnetic material, ferromagnetic composition and a system and method of applying the material to a substrate
US20100098921A1 (en) * 2008-10-14 2010-04-22 Sandvik Innovations, Llc Magnetic load supporting inks

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US4357164A (en) * 1979-12-11 1982-11-02 Sakata Shokai, Ltd. Ink composition for waterless lithography and methods of printing therefrom
FR2618084B1 (en) * 1987-07-15 1989-11-10 Rhone Poulenc Chimie MAGNETISABLE MICROSPHERES BASED ON POLYSILOXANE, THEIR PREPARATION PROCESS AND THEIR APPLICATION IN BIOLOGY

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US2875152A (en) * 1955-12-20 1959-02-24 Shell Dev Process for the preparation of greases gelled with non-soap gelling agents
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US607875A (en) * 1898-07-26 Process of producing magnetic oxid of iron
US1960899A (en) * 1929-07-05 1934-05-29 A V De Forest Associates Magnetic testing material and method of preparing the same
US2232352A (en) * 1936-04-29 1941-02-18 Rca Corp Production of magnetic material
US2267999A (en) * 1939-03-20 1941-12-30 Robert C Switzer Magnetic testing
US2384579A (en) * 1941-08-20 1945-09-11 Harmon Color Works Inc Iron pigments
US2346968A (en) * 1942-09-15 1944-04-18 Interchem Corp Typographic printing ink
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US2601212A (en) * 1948-11-09 1952-06-17 Gen Aniline & Film Corp Heat resistant magnetic cores and method of making
US2684909A (en) * 1951-09-11 1954-07-27 Time Inc Zein ink vehicle
US2688649A (en) * 1951-12-14 1954-09-07 Bjorksten Res Lab For Electroc Printed battery and method for making
US2800458A (en) * 1953-06-30 1957-07-23 Ncr Co Oil-containing microscopic capsules and method of making them
US2920042A (en) * 1955-03-28 1960-01-05 Texaco Inc Method for preparing water resistant grease and hydrophobic finely-divided solids
US2875152A (en) * 1955-12-20 1959-02-24 Shell Dev Process for the preparation of greases gelled with non-soap gelling agents

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3294686A (en) * 1966-12-27 Pigment particles coated with organo-alumtnum compounds
US3247117A (en) * 1960-05-06 1966-04-19 Dick Co Ab Magnetic lithographic ink
US3185589A (en) * 1961-12-21 1965-05-25 Ibm Method of coating finely divided metal particles
US3207622A (en) * 1962-03-05 1965-09-21 Standard Oil Co Method of producing hydrophobicorganophilic magnetic pigments
US3519452A (en) * 1967-03-09 1970-07-07 Cabot Corp Sulfonated carbon black pigmented compositions
US3547822A (en) * 1968-02-01 1970-12-15 Eastman Kodak Co Scum-retardant carrier particles and compositions thereof
US4018601A (en) * 1969-06-19 1977-04-19 Xerox Corporation Electrostatographic magnetic brush imaging process employing carrier beads comprising high purity nickel
US4025690A (en) * 1970-07-06 1977-05-24 Reagens S.P.A. Industria Chimica Method of preparing additives and additives prepared according to said method
US3947371A (en) * 1972-11-21 1976-03-30 Xerox Corporation Developer material with poly(p-xylylene) coated carrier
US3905935A (en) * 1973-01-15 1975-09-16 Hercules Inc Dye laking resins for printing inks
US3929657A (en) * 1973-09-05 1975-12-30 Xerox Corp Stoichiometric ferrite carriers
US4107063A (en) * 1977-03-02 1978-08-15 International Business Machines Corporation Water based selectable charge magnetic inks
US4285994A (en) * 1977-08-17 1981-08-25 Johnson, Matthey & Co., Limited Process for production of free flowing dust-free pigments
US5127952A (en) * 1986-10-10 1992-07-07 Rohne-Poulenc Chimie Core/oxide/dye pigmentary colorants
US20050046176A1 (en) * 2003-08-26 2005-03-03 Crum Jesse D. Communication substrates having variably applied ferromagnetic material, ferromagnetic composition and a system and method of applying the material to a substrate
US6977114B2 (en) * 2003-08-26 2005-12-20 Ward/Kraft, Inc. Communication substrates having variably applied ferromagnetic material, ferromagnetic composition and a system and method of applying the material to a substrate
US20100098921A1 (en) * 2008-10-14 2010-04-22 Sandvik Innovations, Llc Magnetic load supporting inks

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GB935541A (en) 1963-08-28
CH397735A (en) 1965-08-31

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