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
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
  • G03G13/00—Electrographic processes using a charge pattern
  • G03G13/06—Developing
  • G03G13/08—Developing using a solid developer, e.g. powder developer
• • 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
  • G03G9/103—Glass particles

Definitions

• Electrophotographic material usually consists of a support on which there is a coating of a photoconductor, this coating being provided in the absence of light with an electrostatic charge. Then, the material is exposed to light behind a master by the contact process, or an episcopic image is projected thereon, so that an electrostatic image is formed which corresponds to the master.
• the image is developed by being briefly contacted with a resin powder, whereupon a visible image is formed- Which is fixed by heating or by the action of solvents. In this way, an image of the master, which is resistant to abrasion, is obtained electrophotographically.
• the present invention relates to developers of a special kind for such electrophotographic processes.
• the developers normally consist of a mixture of a carrier the material used may be grains of inorganic materials such as fine glass balls or iron filings, or crystals of inorganic salts such as common salt or potassium chloride.
• the material used may be a resin powder containing dyestuffs or pigments, e.g., car bon black.
• the toner When using the developer, the toner acquires a charge opposite to that of the carrier material as a result of fric-. tional electricity. Thus, all the powder is loosely held by the carrier material so that the two components do not separate.
• the developer is scattered over an electrostatic image, the toner particles are attracted to the image being developed, if it has a charge of the opposite polarity to that of the toner. If the electrostatic image and the toner have charges of the same polarity, the toner particles accumulate on the discharged portions of the electrophotographic material.
• the known developers contain, in addition to the carrier, either a toner which acquires a charge which is positive with respect to the carrier material or one which acquires a charge which is negative with respect to the carrier.
• a toner which acquires a charge which is positive with respect to the carrier material
• one which acquires a charge which is negative with respect to the carrier is developed.
• a developer for electrophotographic purposes consisting of a carrier and two distinguishable toners, one of which acquires a positive charge with respect to the carrier and one of which acquires a negative charge with respect to the carrier.
• the two toners are distinguishable we mean that they have characteristics such that the portions of the developed image to which the toners respectively adhere will be distinguishable.
• the toners may differ in color or shade, or one toner may be glossy, while the other has a mat appearance, especially after fixing.
• one of the toners may be fluorescent and thus distinguish from the other.
• the carriers used for the developers in accordance with the invention may consist of grains of inorganic materials, e.g., tiny glass or quartz balls, or fine particles of metals, e.g., iron, copper, and brass, or crystals of inorganic salts such as potassium sulfate, potassium chloride, sodium chloride, copper sulfate, or grains of organic materials, e.g., polystyrene and carboxymethyl cellulose; glass balls covered with organic resins, or crystals of organic compounds such as oxalic acid, adipic acid or phthalic anhydride. Glass balls and also iron powder have proved particularly suitable as carrier materials for the developer in question because of their high density and their mechanical stability.
• inorganic materials e.g., tiny glass or quartz balls, or fine particles of metals, e.g., iron, copper, and brass, or crystals of inorganic salts such as potassium sulfate, potassium chloride, sodium chloride, copper sulfate, or grains of organic materials,
• the carriers generally have a particle size in the range of about to about 600 Smaller or larger carrier particles may be used, but carriers with the larger portion of the particles in the range mentioned, preferably from about 200 to 400 i, have proved advantageous.
• Materials suitable as positive toners for the developer in accordance with the invention include natural and synthetic resins, e.g., colophony, copals, dammar resin, asphalt, colophony-modified phenol resins, ketone resins, maleic resins, coumarone resins, polyacrylic acid resins and polystyrenes. Also, mixtures of these resins can be used.
• natural and synthetic resins e.g., colophony, copals, dammar resin, asphalt, colophony-modified phenol resins, ketone resins, maleic resins, coumarone resins, polyacrylic acid resins and polystyrenes. Also, mixtures of these resins can be used.
• Inorganic and/or organic pigments and/or dyestufls may be mixed with these resins, as well as fluorescent agents.
• the following are, for example, suitable: carbon black, zinc oxide, titanium dioxide, barium sulfate, red lead, Helio-red, Helio-blue, Sudan dyestuffs, Cellitone dyestuffs, spirit-soluble Nigrosine, Pigment Black, Alizarin Blue- Black B, Diamond Black F, Fanal Violet LB and also mixtures of such dyestulfs and/or pigments.
• Suitable waxes for this purpose include natural waxes such as carnauba wax, beeswax, Japan wax, montan wax, and ceresine, and synthetic waxes such as those known under the trade names A-Wachs, OP-Wachs, SPO- Wachs, V-Wachs, O-Wachs, E-Wachs, Hartwachs H, Hartwachs W, various of the waxes known as Ruhr-Wachse and, particularly, the products commercially available under the name of Gersthofener Wachse with the codings S, L, O and OP.
• the low melting point organic compounds that are particularly of interest are substituted and unsubstituted aromatic compounds having a melting point of between about 40 and C.
• Such compounds include naphthols, e.g., l-naphthol and Z-naphthol, and also aromatic compounds such as acenaphthene, acylamino compounds such as acetanilide, aromatic halogen compounds such as p-dibromobenzene, amino compounds such as 2,4-diaminotoluene, o-phenylenediamine, and phenols such as resorcinol and diphenylamine and its derivatives.
• aromatic compounds such as acenaphthene, acylamino compounds such as acetanilide, aromatic halogen compounds such as p-dibromobenzene, amino compounds such as 2,4-diaminotoluene, o-phenylenediamine, and phenols such as resorcinol and diphenylamine and its derivatives.
• metal resinates and. vinyl chloride interpolymers containing carboxyl groups are particularly suitable.
• Metal resinates also known as resin soaps, are to be understood to cover metal salts of resin acids, the metals being those of groups 1 to 8 of the Periodic Table.
• the compounds of particular interest are metal resinates, and mixtures thereof, involving metals such as aluminum, barium, lead, calcium, cerium, iron, cobalt, copper, magnesium, manganese and zinc.
• resins such as are used in the preparation of the positive toners may be added to the negative toners.
• quantities of the waxes and low melting point organic compounds, with a melting point between about 40 and 150 C. may be added to the metal resinates.
• dyestuffs and pigments those described for the positive toners may be used. However, in general, the content of pigments and dyestuffs should not exceed 10% by weight of the metal resinates if the negative charging characteristics are to be adequately maintained.
• dyestuffs containing metals are used, quantities of up to about 50% by weight but preferably not more than 35%, can be used.
• dyestuffs with metal content those may be mentioned which, for example, contain metals such as copper, zinc, magnesium, iron, sodium or potassium incorporated in complex form in the molecule. They include complexes such as chlorophyll or copper, zinc or magnesium phthalocyanines or Naphthol Green B.
• double salts of dyestuif molecules e.g., zinc chloride double salts of Toluidine Blue 0, Methylene Green B or Acridine Orange 2G may be considered, as also complexes of heteropoly acids such as phosphomolybdotungstenic acid with dyestuffs, e.g., the substances known as Fanal dyestuffs such as Fanal Red 6 B, Fanal Violet LB and Fanal Blue B.
• metal salts of sulfonic and carboxylic acids of dyestuffs may be considered, e.g., Alizarin Blue Black B, and Diamond Black F.
• the metal resinate toners are advantageously prepared as follows: the pulverized starting materials are ground together very finely; the mixture is heated until melted, stirred until a high degree of homogeneity is achieved and then the melt is cooled. It is also possible for the fusible starting materials to be liquefied by heating and the remaining components added with stirring; the mixture is then cooled. The toner mass thus obtained is finely ground and then screened. Fractions of an average particle size of about to 100p, preferably about 5 to 30p, are used for the toner.
• the interpolymers may also be colored.
• dispersion dyestuifs Cold Index, vol. 1, pages 16551742
• which are used. for the coloring of polyvinyl chloride may be employed, e.g. Cellitone, Cibacete and Setacyl dyestuffs.
• organic pigments having properties that are physically related to those of the dispersion dyestuffs may also be used for coloring the interpolymers, e.g., fat dyestuffs such as Sudan dyestuffs or development dyestuffs of the Naphthol AS series.
• fluorescent agents may be added. in small amounts to one of the above toners, either alone or in combination with dyestuffs or pigments.
• fluorescent agents there may be used organic aromatic or heterocyclic multinuclear uncolored or colored compounds, which are known per se.
• a carrier e.g., phenylethylurethane, p-chlorotoluene or 2,6-dibromo-toluene
• This carrier is used in quantities of from 1 to 6 percent, preferably 4-6 percent, with respect to the quantity by weight of the interpolymer used.
• the material is then sieved and a fraction with an average particle size of about 1 to preferably 5-30p, is used as toner.
• one of the carriers mentioned is mixed with at least one of the negative and one of the positive toners.
• the proportion of carrier to toner should be in the range of about 100210 to about 10020.1, preferably from about 100:2 to about 100:1.
• the toners can be used in very varied proportions but preferably in proportions of about 1:1 to about 110.1.
• the proportions will be selected so that they approximate the proportions of electrostatically charged areas to discharged areas of the photoconductor coating being developed.
• a high proportion of negative toner will be selected for the developer.
• the developer falling within the scope of the invention has the advantage of enabling an electrostatic image to be developed in two colors or be otherwise distinguished in the image and non-image parts. Also, it is possible, if a black toner and a white toner are used, for a black and white copy to be produced, even if the photoconductor material is colored.
• the red-colored material is finely ground in a ball mill and then sieved. A fraction with a grain size of 2040 is used as toner.
• the solidified melt is ground in a ball mill and then sieved. A fraction containing particle sizes of from 20-30u is used for the toner.
• red toner (a) and 2 parts by weight of the black toner (b) are mixed with 200 parts by weight of glass balls of a diameter of about BOO 1..
• the red toner takes on a negative charge and the block toner a positive charge.
• an electrophotographic material e.g., a paper having zinc oxide incorporated in a resin as a photoconductor coating, or an aluminum plate coated with zinc oxide incorporated in a resin, is negatively charged by means of a corona discharge of 6000-7000 volts.
• the photoconductor coating is exposed to light behind a master and then the developer described is scattered over the surface.
• the red toner adheres to the portions struck by light and the black toner adheres to the negatively charged image parts.
• a copy in black and red becomes visible and is fixed by heating.
• Example 2 A paper having a zinc-oxide photoconductor coating and sensitized with Rhodamine B extra is provided with a negative electrostatic charge by means of a corona discharge in the manner described in Example 1 and is then exposed to light under a master. After development, fixing by heating is performed.
• the developer used is prepared as follows:
• toner (a) and 5 parts by weight of toner (b) are mixed with 100 parts by weight of iron powder and passed by means of a bar magnet over the electrostatic image.
• the negatively charged, black toner adheres to the portions struck by light, while the white, positively charged toner is attracted by the negative charge of the photoconductor coating. In this way, a reversed image of the master is obtained.
• the electrophotographic material, which has been colored red by the sensitizer, is substantially covered by the white toner.
• Example 3 parts by weight of a zinc resinate with a melting temperature (Kofier-Heizbank) 150/ l40-125 C. and an acid number of 0 (Erkazitharz RF) are finely ground, mixed with 1 part by weight of copper phthalocyanine and then melted.
• the cold melt is ground in a ball mill and then seived.
• a fraction of this toner with an average particle size of about 30-50 is used, when used with a glass carrier it acquires a negative charge.
• a ketone resin with a melting point of 76-82 C., a color number of 1-2.5 and an acid number of 0 (Kunstharz AP)
• 0.5 part by weight of montan wax, 0.25 part by weight of acetanilide, and 1 part by weight of Helio-red are melted together.
• the melt is ground in a ball mill and then sieved. A fraction with a particle size of 30 to 50 is used.
• the photoconductor material treated in the manner described in Example 1 with the developer detailed above, consists of a paper which is coated with the organic semiconductor, 2,5 bis [4'-diethylaminophenyl-(1')]-l.3.4- oxadiazole, as described in Belgian Patent 558,078.
• Example 4 10 parts by weight of a low melting point polystyrene and 10 parts by weight of a maleic resin having a melting point range from 69-77" C., an acid number of 32, and a dye number of 9-10, one part by weight of spirit-soluble Nigrosine, and 0.3 part by weight of Pigment Black are mixed and then melted together. After cooling the solidified melt is ground in a ball mill and then sieved. The fraction having an average particle size of about 5-13a is selected for use as a toner. When used with a glass bead carrier it acquires a positive charge.
• Example 5 (a) 30 parts by weight of a low melting point polystyrene, 30 parts by weight of maleic resin having a melting point range from 69-77C., an acid number of 32 and a dye number of 9-10 and 10 parts by Weight of 2,5 bis-[4'-diethylaminophenyl-( l) ]-oxadiazole- 1.3.5) are converted into a homogenous toner by fusion, grinding and sieving. The fraction having an average particle size of about 5-13/L is selected for use as a toner. When used with a glass bead carrier it acquires a positive charge.
• a developer for use in electrophotographic processes comprising a carrier and a toner, one portion of the toner having, with respect to the carrier, 2 positive charge and one portion having a negative charge, the latter portion being selected from the group consisting of metal resinates and vinyl chloride interpolymers containing carboxyl groups.
• a developer according to claim 1 in which the positively charged portion of the toner is selected from the group consisting of natural and synthetic resins.
• one portion of the toner comprises a colored interpolymer of vinyl chloride, vinyl acetate and a dicarboxylic acid, and one portion comprises a colored mixture of a maleinate resin, colophony, polystyrene, and finely divided silicon dioxide.
• one portion of the toner comprises a colored zinc resinate and one portion comprises a colored mixture of a ketone resin, polystyrene, montan wax and acetanilide.
• a process for developing an electrostatic image which comprises contacting the image with a developer comprising a carrier and a toner, one portion of the toner having, with respect to the carrier, a positive charge and one portion having a negative charge, the latter portion being selected from the group consisting of metal resinates and vinyl chloride interpolymers containing carboxyl groups.
• one portion of the toner comprises a colored interpolymer of vinyl chloride, vinyl acetate and maleic acid, and one portion comprises a colored mixture of polystyrene and a maleniate resin.
• one portion of the toner comprises a colored interpolymer of vinyl chloride, vinyl acetate and a dicarboxylic acid, and one portion comprises a colored mixture of a maleinate resin, colophony, polystyrene and finely divided silicon dioxide.
• one portion of the toner comprises a colored zinc resinate and one portion comprises a colored mixture of a ketone resin, polystyrene, montan wax, and acetanilide.
• one portion of the toner comprises a colored interpolymer of vinyl chloride, vinyl acetate, and maleic acid of mat appearance, and one portion comprises a colored mixture of polystyrene and maleic acid of glossy appearance.
• one portion of the toner comprises an uncolored interpolymer of vinyl chloride, vinyl acetate, and maleic acid, and one portion comprises a fluorescent mixture of polystyrene, maleic acid, and 2,5 bis [4'-diethylaminophenyl-(1')-]- oxadiazole-( 1.3.5)

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• General Physics & Mathematics (AREA)
• Developing Agents For Electrophotography (AREA)

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Cited By (31)

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Citations (9)

• 0
  • BE BE594137D patent/BE594137A/xx unknown
  • NL NL254973D patent/NL254973A/xx unknown
• 1959
  • 1959-08-17 DE DEK38460A patent/DE1206306B/de active Pending
• 1960
  • 1960-07-19 US US43734A patent/US3236776A/en not_active Expired - Lifetime
  • 1960-07-28 LU LU39008D patent/LU39008A1/xx unknown
  • 1960-08-03 CH CH881460A patent/CH381983A/de unknown
  • 1960-08-10 GB GB27695/60A patent/GB944394A/en not_active Expired
  • 1960-08-16 SE SE7855/60A patent/SE306667B/xx unknown

Patent Citations (9)

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