Energized liquid developers for developing electrostatic images

Information

  • Patent Grant
  • 4049446
  • Patent Number
    4,049,446
  • Date Filed
    Monday, February 9, 1976
    50 years ago
  • Date Issued
    Tuesday, September 20, 1977
    48 years ago
Abstract
A method of developing electrostatic images in which a liquid developer is maintained in quiescent condition in contact with the base material carrying the electrostatic image and wherein the developer contains in separate coexistence within an insulating carrier liquid toner particles of relatively low dielectric constant and movement-inducing particles having a high dielectric constant. The presence of both sets of particles results in agitation in the liquid due to particle movement in a field by charge exchange between the high dielectric particles and the other particles to produce random agitation of the particles in the liquid and thereby high mobility of the toner particles during developing.
Description

This invention relates to energised liquid developers for developing electrostatic images.
BACKGROUND OF THE INVENTION
Liquid developers usually consist of developer particles suspended in an insulating liquid having a resistivity in excews of 10.sup.10 ohm. c.m. and a dielectric constant less than 3, the developer particles being coated with an insulating medium such as a resin whereby to control the polarity of the particles in the insulating liquid and also to provide the means whereby the rate of exchange of charges between the particles and a surface containing a latent electrostatic image is slowed down, and such resin or other insulating medium can also be such that on the position an evaporation of a carrier liquid this forms a fixing medium for the particles.
Such a developer is already well-known and various applications by the applicant have proceeded to the grant of patents and have been brought into commercial use.
One of the problems associated with developers of this type is that the particles tend to settle out, this settling increasing with a coarseness of the particles and thus it has been customary to prepare the developer in the form of a relatively thick paste and to break down the developer by adding the carrier liquid just prior to use on the developer, the paste being thoroughly mixed into the carrier liquid so that at the time of development the particles of toner or developer medium are uniformly dispersed throughout the carrier liquid.
It has been shown in the past that improved development results where there is agitation of the developer just prior to it being applied and also that improved images result where the developer is agitated at the time of application to the surface containing the latent electrostatic image, and to achieve this it has been proposed to apply the developer liquid to the surface with a washing action so that the surface is swept by the developer for a required time to ensure that sufficient particles are brought into the image field to deposit to give an image of a required density.
SUMMARY OF THE INVENTION
We have now found that a developer such as that described can be improved by including in the developer formulation, as well as toner particles, conductive particles which move rapidly in a field and thus act to keep the developer particles in relatively rapid motion when both the developer particles and the conductive particles co-exist in the carrier liquid. The basis of the invention is that conductive particles, such as metal particles, can readily exchange charges with a surface containing a latent image or with other particles and can thus alternate rapidly under such conditions.
Thus the image which is to be developed may have a negative characteristic and if the conductive particles have an inherent positive characteristic in the carrier liquid, which can be given to them by a control coating on the surface, they will be drawn down to the negative field area, but because they are able to exchange charges, they will, on approaching the surface, interchange charges with the surface and as they become sufficiently negative will be repelled from the surface, but as they leave the influence of the negative field they are again able to exchange charges with other conductive particles or other areas and will again become relatively positive in relation to the image charge so that they will be again drawn to it but immediately repelled on an exchange of the charges.
In this way the developer contains toner particles which are inherently insulators, such as coloured dyed particles, and which are not able to readily exchange charges and thus go down on the image and remain there sufficiently long to provide the necessary developed image as has been referred to in numerous patents already on record, but by having a developer mixture which also contains particles of high conductivity even if partial control is exerted by a surface layer of resin, the developer is now activated or energised when in the presence of a field because the conductive particles tend to move on to and then away from the surface containing the field and during this action affect a stirring or energising of the developer to ensure that there is a rapid movement in all of the particles through collisions and the like and development takes place as it were by means of a developer which is in an agitated state so soon as it is applied to a surface having a latent electrostatic image. Metal particles are envisaged having a high dielectric constant so that even if coated by an insulator the conductive characteristic will predominate.
In this connection it is important to remember that short and long range interactions with a centre occur in all cases, but short range interactions dominate for tightly bound electrons in low dielectric constant materials, but long range interactions dominate in high dielectric constant materials, thus making it possible to use even coated high dielectric constant materials such as the metals of the examples.
In this connection it should be remembered also that when a surface contains a latent electrostatic image with the image being formed of one polarity, those areas which are not image areas are relatively of opposite polarity and therefore because this relativity, the conductive particles are assured rapid motion.
It will be appreciated that if the photosensitive surface is itself highly insulating, charge exchanges with the surface cannot take place, but as an image field exists which extends from the surface, the conductive particles are influenced by the field itself.
Alternatively the surface is made less insulating by including in the photosensitive layer some conductive particles or solvents which affect conductivity, which can readily be influenced by the image field as they exist in the insulating layer which supports the field and these conductive inserts or inclusions then form ready charge exchange means with the conductive particles in the developer.
For this reason coatings are suggested which when used in conjunction with the developer, enhance the effect thereby.





The following examples show how developers having this energised effect can be formulated.
EXAMPLES OF COATINGS
Electrophotographic coatings may be produced as follows:
______________________________________Coating A______________________________________Isojordosol 4501/60 short oil alkyd resin 430 grams(Jordan Chemicals)Zinc oxide (colloidal grade) 158 grams(Durham)Aluminium bronze 1 gramRose Bengal (sensitiser dye) 0.2 gramsToluol 1200 millilitersThese materials were ball milled together to form acoating composition.Cobalt and zinc naphthenate driers were added (0.5%and 0.5% by wt. of solid resin).______________________________________
This coating can be applied to either film, metal backing or paper.
______________________________________Coating B______________________________________Styrene-butadiene copolymer Esso polymer 200(Buton 200) 150 gramsZinc oxide 500 gramsLead naphthenate 6% solution in mineral spirits 1.0 gramCobalt naphthenate 6% solution in mineral spirits 0.1 gramNickel powder 1 gramZirconium octoate 6% solution in mineral spirits 1 gramCerium octoate 6% solution in mineral spirits 0.05 grams______________________________________
The naphthenate and octoates increase the conductivity.
______________________________________Solvent Alsol 95/130 900 millilitersToluol 65 millilitersHexyl acetate 10 millilitersEthyl acetate 10 millilitersButanol 10 millilitersPentoxone 5 millilitersDisulphine Blue 1% by wt. in methyl alcohol 2 millilitersAcridine Orange 1% by wt. in methyl alcohol 2 millilitersErythrosin B 1% by wt. in methyl alcohol 2 millilitersSodium fluorescein 5 milliliters______________________________________
The latter materials form sensitisers in different wave lengths.
These materials are ball milled together and dip coated on paper, metal, wood, or film base to form a photoconductive layer.
______________________________________Coating C______________________________________Jordosol 2232/50 short oil alkyd resin 400 grams(Jordon Chemicals)Zinc oxide (colloidal grade) 1200 grams(Durham)Bromocresol Green 0.5% by wt. in methyl alcohol 10 millilitersBromophenol Blue 0.5% by wt. in methyl alcohol 10 millilitersSodium Fluorescein 1% by wt. in methyl alcohol 10 millilitersErythrosin B 1% by wt. in methyl alcohol 10 millilitersCobalt Naphthenate 6% solution 0.1 gramsZinc Naphthenate 3% solution 1.0 gramsSolvent (Esso) Alsol 95/130 2,000 milliliters______________________________________
These materials are ball milled together to form an electrophotographic coating composition having a relatively high conductivity and increased sensitivity due to greater colour absorption.
______________________________________Coating D______________________________________Mowital B 30 H (Polyvinyl Butyral resin) 100 grams(Hoechst)Zinc Oxide - special z grade 1000 grams(Durham)______________________________________
The Mowital was taken up in 800 milliliters of methyl ketone and 200 milliliters of methyl alcohol and ball milled with the zinc oxide which was previously dyed with the following:
______________________________________Sodium Fluorescein 1% solution in methanol 10 millilitersErythrosin B 1% solution in methanol 5 millilitersRose Bengal 1% solution in methanol 2 millilitersBromocresol Green 0.5% solution in methanol 5 millilitersBromophenol Blue 0.5% solution in methanol 5 milliliters______________________________________
This coating composition was let down with 500 milliliters of methyl ethyl ketone solvent and 500 milliliters of perchloroethylene to form the final coating composition.
______________________________________EXAMPLES OF DEVELOPERSDeveloper 1 Negative Black DeveloperKohinoor Carbon Black 100 gramsSunflower seed oil (Meggitts) 300 gramsB.P.V. oil (Viscostatic) (British Petroleum) 500 gramsAlkyd resin (1352/60) Super Beckosol 200 grams(Reichold Chemicals)______________________________________
The above ingredients are milled together and then suspended together with 1 gram aluminum bronze powder in 100 mls. Esso 100 and 1,000 mls Isopar E.
This developer is applied to the latent image on a relatively conductive photoconductive coating and acts as an energised developer with relatively rapid charge exchange effects and consequent high mobility in an image field.
______________________________________Developer 2 Copolymeric Blue DeveloperHostaperm Blue B3G (Hoechst) 100 gramsStyrene-butadiene copolymer 200 gramse.g. "Solprene 1205" (Phillips Imperial Chemicals)Vinyl toluene-acrylate copolymer 100 gramse.g. "Pliolite VTAC" Australian SyntheticRubber Co.Zinc powder, 1 micron mean diameter 1 gram______________________________________
The copolymeric resins were taken up in Solvesso 100 and subsequently milled with the blue pigment.
______________________________________Developer 3(Copolymeric suspension in Isopar E (Esso),and isoparaffinic hydrocarbon solvent).Isopar E 200 mls."Solprene 1205" 5 grams(solution of 1 gram of solid in 2 mls.)"Pliolite VTAC" 5 grams(solution of 1 gram of solid in 2 mls.)0.1 parts by wt.Aluminium powder 1 gram______________________________________
The developer can be applied by a simple electrode or by a roller.
______________________________________Developer 4BlueGraphtol Blue BLF. (Sandoz) 54 gramsSolprene 1205 20 gramsVTAC 10 gramsNickel powder 1 gramDispersed in:Esso 100 100 mls.Isopar E 1000 mls.Developer 5Hostaperm Blue B3G (Hoechst) 54 gramsSolprene 1205 61 gramsVTAC 32 gramsCopper powder 0.5 gramsDispersed in:Esso 100 100 mls.Isopar E 1000 mls.Developer 6Graphtol yellow 4813 - 0 (Sandoz) 40 gramsSolprene 1205 20 gramsVTAC 10 gramsIntermetallic compound powder 0.5 gramsDispersed in:Esso 100 100 mls.Isopar E 1000 mls.Developer 7Permanent yellow GG (Hoechst) 40 gramsSolprene 1205 10 gramsVTAC 7 gramsTin powder 0.5 gramsDispersed in:Esso 100 100 mls.Isopar E 2000 mls.Developer 8Graphtol Red 1630 60 gramsSolprene 1205 10 gramsVTL Copolymer 10 gramsIron powder 0.5 gramsDispersed in:Esso 100 100 mls.Isopar E 2000 mls.Developer 9Isol Ruby Red 50 gramsBrillfast Rose Red 30 gramsPale lowering Lithographic Varnish 20 gramsRhodene alkyd resin L42/70 200 gramsNickel powder 0.5 gramsDispersed in:Esso 100 100 mls.Isopar E 2000 mls.Developer 10Isol Ruby Red 50 gramsBrillfast Rose Red 30 gramsAlkyd resin P470 105 gramsBeeswax 12 gramsToluene 15 mls.Chromium powder 0.5 gramsDispersed in:Esso 100 mls.Isopar E 1000 mls.Developer 11Aluminium bronze metal powder 100 gramsAlkyd Resin P470 20 gramsToluene 15 mls.Dispersed in:Esso 100 50 mls.Isopar G 1000 mls.______________________________________
It is to be noted that in developer 11 the aluminum bronze metal powder additive can be replaced by silver, zinc, aluminum, iron, chromium, copper tin or other metal powder and also that the resin can be replaced by other alkyd resins, or by phenolformaldehyde, polymers, or shellac, polyethylene, polyisobutylene, polyisoprene, polyvinylacetate, polymethylmethacrylate, cellulose, ethyl cellulose, ethyl hydroxy ethyl cellulose, cellulose acetate, polyvinylchloride, polyvinyl chlorinated rubber, polyamides, polyesters or the like and further that this developer may be used as a dispensible additive in other developers.
CHEMICAL REFERENCES
ISOJORDOSOL 4501/6 short oil alkyd resin (Jordan Chemicals) oil length 50%, specific gravity 0.99-1.00, oil type safflower, Viscosity G.H, WX. Acid No. 5-10.
JORDOSOL 2232/50 a short oil alkyd resin (Jordan Chemicals) oil length 40%, specific gravity 1.020, oil type D.C.O. Viscosity G-H, Z-Z1, Acid No. 15-20.
MOWITAL B30H polyvinyl butyral resin, made by Hoechst, Germany; containing polyvinyl acetal 76-78 percent polyvinyl acetate 1 percent and polyvinyl alcohol 18-21 percent.
B.P.V. OIL synthetic automotive lubricating oil containing anti-oxidant "ZDP," dialkyl zinc dithiophosphate in solution, made by British Petroleum Ltd.
HOSTAPERM BLUE B3G copper phthalocyanine blue, pure beta-form, made by Hoechst, C.I. pigment Blue 15, Colour Index No. 74,160.
SOLPRENE 1205 is a block co-polymer of butadiene and styrene in the ratio of 75/25 manufactured by the Solution Polymerization process. Contains 97.5 Rubber Hydrocarbon. It is stabilized by addition of 1% of a non-staining anti-oxidant.
Max IBM Colour 3 (Phillips Imperial Chemicals Ltd.)
PLIOLITE VT RESIN is a styrene/butadiene type copolymer rubber made by Goodyear Corp., U.S.A. and prepared by the "G.R.S." method in which the butadiene polymerises in the main by a 1,4-addition. Pliolite VT is a vinyl toluene/butadiene random copolymer rubber soluble in mineral spirits.
GRAPHTOL YELLOW MONO AZO Dye Stuff Pigment, by SANDOZ LTD, Switzerland, C.I. Pigment 66, C.I. 1,800-1.
PERMANENT YELLOW 66 extra, a diazo yellow pigment without lake forming groups, C.I. pigment yellow 17, Colour Index No. 21105.
GRAPHTOL RED MONO AZO DYE BY SANDOZ LTD. Switzerland C.I. Pigment 1, C.I. 11,000-680.
ISOL RUBY RED BKS 7520 (KVK) a lithol ruby red C.I. Pigment Red 57, Agfa, Calcium lake.
RHODENE ALKYD RESIN L42/70 a pure drying long oil alkyd resin (Polymer Corp.) oil length 64%, oil type safflower, specific gravity 0.957, Viscosity (G-H) 4-7, Acid No. 6-10.
BECKOSOL ALKYD RESIN P470/70 a pure drying long oil alkyd resin (Hatrick) Oil length 65%, oil type Soya, specific gravity 0.955, Viscosity (G-H) Z1-Z2, Acid No. 3-7.
ISOPAR E a hydrocarbon solvent (Esso Chemicals) boiling range 117.degree.-144.degree. C., Aromatic content 0.05, flash point upward 73.degree. F., Specific gravity 0.723.
ISOPAR G a hydrocarbon solvent (Esso Chemicals) boiling range 158.degree.-177.degree. C., aromatic content 0.20, flash point 103.degree. F., specific gravity 0.750.
SOLVESSO 100 a hydrocarbon solvent (Esso Chemicals) boiling range 156.degree.-171.degree. C., aromatic content 98.9, flash point 110.degree. F., specific gravity 0.874.
Claims
  • 1. A method of developing electrical field images which comprises applying a developer to a base material having a coating comprising a photosensitive medium and a resin having embedded therein particulate conductive particles or a medium which increases the conductivity in the proportion by weight of 100 to 500 grams of resin to 0.5 to 2 grams of conductive material to form a membrane capable of sustaining a latent electrostatic image, said developer being an energized liquid developer comprising in separate co-existence within an insulating liquid of (a) toner particles of relatively low dielectric constant arranged due to their electrical characteristic to deposit on selected image areas and (b) movement-inducing high dielectric constant metallic powder particles which have a rapid charge exchange with other particles and adjacent surfaces to cause the said high dielectric particles to oscillate between other particles and the said surfaces whereby by collisions of said particles and the toner particles to introduce random agitation of particles in the liquid and by the presence of the photoconductive particles in the photosensitive base, and the metallic particles in the carrier liquid of the developer, agitation is enhanced at the interface between the liquid and the photoconductor due to charge exchange between the fixed conductive particles in the photoconductor and the moving metal particles in the developer liquid, maintaining said body of developer itself quiescent except for the random particle movement, said toner particles being colored resin particles, said metal powders being selected from the group consisting of aluminum, bronze powder, zinc powder, aluminum powder, copper powder, intermetallic compound powder, tin powder, iron powder, and chromium powder.
  • 2. The method of claim 1 in which said toner particles comprise a coloring medium in particulate form having a resin control coating on said particles formed by milling toner medium in the presence of a dissolved resin.
Priority Claims (1)
Number Date Country Kind
691/72 Oct 1972 AU
CROSS RELATED APPLICATION:

This application is a division of copending application Ser. No. 401,966 filed Sept. 28, 1973, now abandoned, and claiming the priority of the application filed in Australia on Oct. 4, 1972.

US Referenced Citations (5)
Number Name Date Kind
3078231 Metcalfe et al. Feb 1963
3406062 Michalchik Oct 1968
3766072 Metcalfe et al. Oct 1973
3793015 Van Engeland et al. Feb 1974
3811914 Saito et al. May 1974
Foreign Referenced Citations (2)
Number Date Country
1,070,718 Jun 1967 UK
1,214,150 Dec 1970 UK
Divisions (1)
Number Date Country
Parent 401966 Sep 1973