Classifications

• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
  • G03G9/00—Developers
  • G03G9/08—Developers with toner particles
  • G03G9/10—Developers with toner particles characterised by carrier particles
  • G03G9/107—Developers with toner particles characterised by carrier particles having magnetic components
  • G03G9/1075—Structural characteristics of the carrier particles, e.g. shape or crystallographic structure
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
  • G03G9/00—Developers
  • G03G9/08—Developers with toner particles
  • G03G9/10—Developers with toner particles characterised by carrier particles
  • G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
  • G03G9/1132—Macromolecular components of coatings
  • G03G9/1133—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
  • Y10T428/2991—Coated
  • Y10T428/2998—Coated including synthetic resin or polymer
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31678—Of metal
• • Y—GENERAL 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
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31678—Of metal
  • Y10T428/31692—Next to addition polymer from unsaturated monomers

Definitions

• Color electrophotography with multiple development techniques is capable of producing color reproductions employing multiple sequencing of electrophotographic charging, exposing, and developing steps with color toners.
• a suitable photoconductor such as substantially panchromatic zinc oxide photoconductive paper, electrofax paper, for example, is electrostatically .charged uniformly in the dark then exposed through a green filter to an imagewise projection of a color image to form anelectrostatic latent image on the photoconductor.
• the electrostatic latent image is then developed with the complementary magenta colored toner to form a magenta-colored image corresponding to said electrostatic latent image and transferred in register to an image receiving member.
• a zinc oxide photoconductive paper is then again electrostatically charged uniformly in the dark and then exposed through a red filter to an imagewise projection of a color image in register with said magenta developed image to form a second electrostatic latent image which second image is developed with the complementary cyan-colored toner and likewise transferred in mg ister.
• zinc oxide photoconductive paper is again electrostatically uniformly charged in the dark and then exposed through a blue filter to an imagewise projection of a color image in register with said magenta and cyan-developed images to form a third electrostatic latent image which is then developed with the complementary yellow toner and again transferred in register.
• This conventional electrophotographic process with superimposed development to obtain images of cyan, magenta, and yellow, respectively, is capable of producing multicolor images by employing toners of different colors.
• the sequence of exposures through color filters in this multiple development process may be performed in any suitable sequence other than the green, red, and blue sequence recited above. In any event, after the desired number of exposures and developments and transfers in register, the finished image is itself fused to provide a permanent reproduction of the original.
• Each developer employed comprises ordinarily a toner or a resin colorant mixture in combination with a carrier. It is a function of the toner carrier combination or developer package in a given development system, for example cascade, to assume a triboelectric relationship such that the toner will be carried with the carrier during the development cycle by electrostatic attraction and then selectively deposited charge-wise on the electrostatic latent image which has a greater affinity for the. toner electrostatically than does the carrier particle. In addition to the very significant triboelectric properties that a developer must possess and maintain during the development cycle, the toner must possess the appropriate color and continue to function under machine conditions which expose the developer to impaction and humidity among other undesirable factors.
• Still another object of this invention is to provide a novel magenta developer for use in a color electrophotographic imaging process.
• Yet another object of this invention is to provide a novel color electrophotographic imaging process.
• Yet again another object of this invention is to provide a trichromatic electrophotographic imaging process of the registration type.
• a threedeveloper package including a magenta toner, 2,9- dimethyl substituted quinacridone toner and a nickel berry carrier; a cyan toner, copper tetra-4- (octadecylsulfonomido) phthalocyanine and a methyl terpolymer coated steel short carrier; and a yellow toner, diarylide yellow 3,3-dichlorobenzidine acetoacetanilide with a methyl terpolymer coated steel shot carrier.
• xerographic imaging processes there are numerous known carrier materials from which to select in providing a developer, i.e., a toner and a carrier combination.
• a toner and a carrier combination there are numerous known carrier materials from which to select in providing a developer, i.e., a toner and a carrier combination.
• color electrophotographic imaging the selection of appropriate carrier material is not just a matter of choice.
• steel shot may be employed with the cyan and yellow toner materials disclosed above; however, steel shot is found to be inoperable with the magenta toner therefore necessitating the discovery of an appropriate carrier, namely nickel berry, to perform this function.
• an appropriate carrier namely nickel berry
• a colorant and resin combination must be selected such that the color, of course, is the appropriate hue, but more significantly that the toner possesses the appropriate triboelectric properties which will enable it to function in an electrophotographic automatic imaging mode. Few, if any, of these toner materials are known other than those disclosed above. It, therefore, becomes even a more demanding and crucial operation .cal resin to develop the appropriate combination of toner and carrier so that they will develop and maintain the appropriate triboelectric relationship further complicated by employing these color developers in combination in an electrophotographic imaging process.
• the carrier employed with both the cyan and yellow toners is a methyl terpolymer coated steel shot.
• the steel shot carrier is about 100 microns in diameter as compared to .the cyan and yellow toner particle sizes which are about 16 microns.
• the magenta toner is combined with a nickel berry carrier having a size of about 100 microns as compared to the magenta toner which has a size of about 16 microns.
• the developer package thus provided is usually disposed in three separate developer housings in an automatic color electrophotographic imaging machine.
• a photoconductive member is then charged, selectively exposed to the light of one of the primary colors and then developed with the developer, i.e., the complement to that primary color.
• the image thus formed is then transferred to an image receiving member.
• the process is again repeated to provide images employing the other two primary colors, developing in each case with the complement of the respective primary colors, and then transferring both images in registration to the image receiving member after which the final image is fixed normally by fus-
• the cyan, yellow, and magenta colorants may be combined with any suitable electrophotographic resin.
• the selected colorant may be combined with any typiincluding: thermoplastics including olefin polymers such as polyethylene and polypropylene; polymers derived from dienes such as polybutadiene, polyisobutylene, and polychloroprene; vinyl and vinylidene polymers such as polystyrene, styrene butylmethacrylate copolymers, styrene-acrylonitrile copolymers, acrylonitrile-butadienestyrene terpolymers, polymethylmethacrylate, polyacrylates, polyvinyl alcohol, polyvinylchloride, polyvinylcarbazole, polyvinylethers, and polyvinyl ketones, fluorocarbon polymers such as polytetrafluoroethylene and polyvinylidene fluoride; heterochain thermoplastics such as polyamides, polyester, polyurethanes, polypeptides, casein, polyglycols, polysulfides, and poly
• Typical inorganic photoconductor materials are: sulfur, selenium, zinc sulfide, zinc oxide, zinc cadmium sulfide, zinc magnesium oxide, cadmium selenide, zinc sil-
• Typical organic photoconductors are: triphenylamine; 2,4-bis(4,4-diethyl-aminophenyl)-l,3,4-oxadiazol; N- isopropylcarbazole triphenylpyrrol; 4,5-diphenylimidazolidinone; 4,5-diphenyl-imidazolidinethione; 4,-
• diphenylimidazolidinethione 4-5-bis-(4-aminophenyl)-imidazolidione; 1,5-dicyanonaphthalene; 1,4- dicyanonaphthalene; aminophthalodinitrile; nitrophthalodinitrile; 1,2,5 ,6-tetraazacyclooctatetraene- (2,4,6,8); Z-mercapto-benzthiazole; 2-phenyl-4- diphenylidene-oxazolone; 6-hydroxy-2,3-di(pmethoxy-phenyl)-benzofurane; 4-dimethyl-amino benzylidene-benzhydrazide; 3-benzylidene-aminocarbazole; polyvinyl carbazole; (2-nitro-benzylidene)- p-bromo-aniline; 2,3-diphenyl quinazoline; 1,2,4-
• Typical charging methods include corona, charge deposition resulting from air breakdown in the gap commonly referred to as TESl or charging in vacuo with an electron gun.
• Any suitable method of exposure may be employed in the system of the instant invention.
• Typical methods of exposure include: reflex, contact, holographic techniques, non-lens slit scanning systems, and optical projection systems involving lens imaging of opaguereflection subjects as well as transparent film originals.
• Typical development systems include: cascade development, magnetic brush development, powder cloud development, and liquid development.
• Any suitable method of fixing may be employed in the process of the instant invention.
• Typical methods of fixing include: heat-pressure fusing, radiant fusing, combination radiant, conductive and convection fusing, cold pressure fixing, flash fusing, solvent fusing, and combination heat, pressure solvent fusing.
• the developer compositions of the present invention may be prepared by any well-known developer mixing combination technique. Generally speaking, satisfactory results are obtained when about one part toner is used with about 10 to 200 parts by weight of carrier prepared by blending and milling the components and thereafter micropulverizing the resulting mixture.
• the toner particles may be formed by spray drying, suspension polymerization, hot melt atomizing, or precipitation of a solution of the toner composition.
• the toner mixture of this invention is employed in the cascade development process, the toner should have an average particle diameter of less than about 30 microns and preferably between about 5 and about 20 microns for optimum results. For use in powder cloud development methods, particle diameters of slightly less than about 5 microns are preferred.
• the cyan and yellow toners must be combined with methyl terpolymer coated steel bead carriers while the magenta toner must be combined with the nickel berry carrier in order to provide the highly effective color imaging system of the present invention.
• Cyan, magenta, and yellow toners are prepared which are respectively designated as copper tetra-4- (octadecylsulfonamido)phthalocyanine pigment available from GAF Corporation under the designation of Heliogen Blue OS, a 2,9-dimethylquinacridone pigment identified in the Colour Index as Pigment Red 122 available from American Hoechst Corporation under the designation Hostaperm Pink E, and 3,3- dichlorobenzidine aceto-acetanilide pigment identified in the Colour Index as Pigment Yellow 12 available from Hercules, Inc., under the designation Amazon Yellow X-2485.
• Each colorant is dispersed in a 65/35 styrene to n-butylmethacrylate copolymer. Five parts of each colorant are placed in 95 parts of beads of the toner copolymer resin together to form a homogenous mixture.
• the pigments employed have a particle size essentially less than one micron with occasional agglomerates up to about five microns.
• the mixture is then fed into a twinscrew extruder operating at a temperature of about 150C.
• the extruder softens the copolymer resin, disperses the pigment throughout the molten resin, and extrudes the mixture as a strand of, about /4, inch in diameter;
• the strand is cooled by immersion in a cold water bath and cut to about /4 inch length pellets.
• the pellets are continuously ground in a controlled pressurized air-jet mill to yield toner particles of about 16 microns in size.
• the cyan and yellow toners produced as above are combined with a steel carrier particle coated with a terpolymer material prepared as disclosed in Example XIII of US. Pat. No. 3,526,533.
• the steel carrier has a particle diameter of about 100 microns.
• the cyan toner is blended with the carrier to yield a developer containing about 2 percent toner concentration by weight.
• the yellow toner is blended with the carrier to yield a developer containing about 3 percent toner by weight.
• l H v The magenta toner 1 is blended with an uncoated nickel berry carrier bead to yield a developer containing about 4 percent toner concentration by weight.
• the nickel berry carrier bead employed has a spheroidal shape with a rough pebbly surface and a particle size of about 100 microns and is available from the British Metal Corporation (Canada) Ltd. under the designation Sherritt Nickel Powder, C-Grade. Both the steel andnickel berry carriers employed are magnetic.
• the developers thus produced are disposed in magnetic brush developerhousings which are positioned around a selenium photoconductor.
• the photoreceptor is charged to a positive potential of +1000 volts and exposed to a colorimage through a blue filter.
• the latent electrostatic chargeremaining on the photoreceptor is developed with the yellow developer by engaging the developer housing into development configuration with the photoreceptor.
• the image on the photoreceptor is transferred to a receiver sheet in register.
• the photoreceptor is cleaned of the residual yellow toner and the cycle above is repeated by exposing through a green filter and developing the resulting electrostatic latent image with a magenta developer.
• EXAMPLE n1 The xerographic three-color print process employing the developer s. enumerated in Example I is again repeated with the exception that the magenta developer is replaced by one having 3 percent by weight of magenta toner in combination with a steel carrier coated with the terpolymer composition used for cyan and yel-, low developers. Three-color prints produced are unacceptable .from the initial start-up due to excessive magenta toner deposits on the print and by the 200th copy image reversal occurs. The individual cyan and yellow single-color prints show magenta contamination and are also unacceptable.
• EXAMPLE IV The xerographic three-color print process employing the, developers enumerated in Example I is repeated withtlie exception that the cyan and yellow toners are combined with the uncoated nickel carrier used for the magenta developer of Example I.
• Excellent three-color prints are produced through the initial 500 copies after which the print quality deteriorates because of cyan I and yellow carrier bead adhesion to the photoreceptor surface. This results in deletion of solid area toner coverage, poor line definition, inefficient cleaning, and difficultyin maintaining image density as well as damage to the photoreceptor surface.
• Carrier bead adhesion is attributed tothe high'triboelectric charge of the cyan and yellow toners with-the nickel berry carrier.
• the magenta developer is found to produce single-color copies of good quality. 9
• EXAMPLE V The xerographic three-color print process employing the developers of Example I is again repeated with the exception that the cyan and yellow developers are combined with the uncoated. steel carrier. It is found that good three-color prints are produced through the initial 250 copies after which cyanand yellow print quality deteriorates rapidly and image reversal occurs by the 300th print. As a result, it is found that although the magenta developer continues to produce good single color-print quality, the three-color prints are unacceptable.
• a color electrophotographic imaging process comprising charging a photoconductive member, exposing said photoconductive member to an original to be reproduced through a filter of one color thereby selectively discharging said photoconductive member, developing the electrostatic image formed thereby with a developer of a complementary color, said developer being one member of the group consisting of copper tetra-4-(octadecylsulfonomido) phthalocyanine cyan toner and a methyl terpolymer coated steel carrier, 2,9-dimethyl-quinacridone magenta toner and a nickel berry carrier, and 3,3-dichlorobenzidine acetoacetanilide yellow toner and a methyl terpolymer coated steel carrier; charging said photoconductor for a second time and selectively exposing said photoconductor to the same image through a filter of another primary color, developing the latent electrostatic image formed thereby with a developer of a complementary color,
• said developer being another member selected from the group consisting of copper tetra-4- (octadecylsulfonomido) phthalocyanine cyan toner and a methyl terpolymer coated steel carrier, 2,9-dimethyl-quinacridone magenta toner and a nickel berry carrier, and 3,3-dichlorobenzidine acetoacetanilide yellow toner and a methyl terpolymer coated steel carrier; charging said photoconductive member for a third time, exposing said photoconductor to the same image through a filter of the remaining primary color and developing the latent electrostatic image with a complementary developer, said developer being the remaining developer of the group consisting of copper tetra-4-(octadeeylsulfonomido) phthalocyanine cyan toner and a methyl terpolymer coated steel carrier, 2,9-dimethyl-quinacridone magenta toner and a nickel berry carrier, and 3,3-dichloro

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• Chemical & Material Sciences (AREA)
• General Physics & Mathematics (AREA)
• Crystallography & Structural Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Spectroscopy & Molecular Physics (AREA)
• Developing Agents For Electrophotography (AREA)

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• 1972
  • 1972-12-18 US US00316144A patent/US3804619A/en not_active Expired - Lifetime
• 1973
  • 1973-11-21 CA CA186,415A patent/CA1005678A/en not_active Expired
  • 1973-12-14 GB GB5804973A patent/GB1435218A/en not_active Expired
  • 1973-12-17 NL NL7317284A patent/NL7317284A/xx unknown
  • 1973-12-17 FR FR7345057A patent/FR2210782B1/fr not_active Expired
  • 1973-12-17 DE DE2362667A patent/DE2362667A1/de active Pending
  • 1973-12-18 JP JP14177273A patent/JPS5330496B2/ja not_active Expired
  • 1973-12-18 BR BR9898/73A patent/BR7309898D0/pt unknown

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