US3345161A - Photoconductive material and process for its preparation - Google Patents

Photoconductive material and process for its preparation Download PDF

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Publication number
US3345161A
US3345161A US264759A US26475963A US3345161A US 3345161 A US3345161 A US 3345161A US 264759 A US264759 A US 264759A US 26475963 A US26475963 A US 26475963A US 3345161 A US3345161 A US 3345161A
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US
United States
Prior art keywords
zinc oxide
dyes
dye
photoconductive
electrostatic
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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US264759A
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English (en)
Inventor
Mammino Joseph
Willard C Hamm
Margaret C Pease
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
GAF Chemicals Corp
R Q O HOLDING CO Inc
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General Aniline and Film Corp
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Publication date
Application filed by General Aniline and Film Corp filed Critical General Aniline and Film Corp
Priority to US264759A priority Critical patent/US3345161A/en
Priority to GB7972/64A priority patent/GB1033243A/en
Priority to DEG39993A priority patent/DE1273324B/de
Priority to CH293964A priority patent/CH440977A/de
Priority to FR967108A priority patent/FR1385960A/fr
Priority to NL6402707A priority patent/NL6402707A/xx
Priority to BE645137D priority patent/BE645137A/xx
Application granted granted Critical
Publication of US3345161A publication Critical patent/US3345161A/en
Assigned to R Q O HOLDING COMPANY INC reassignment R Q O HOLDING COMPANY INC ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: GAF CORPORATION
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Expired - Lifetime legal-status Critical Current

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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/09Sensitisors or activators, e.g. dyestuffs

Definitions

  • the present invention relates to photoconductive material and a process for its preparation. It has particular reference to a process for the optical sensitization of photoconductors of variou kinds, and particularly the more commonly used materials such as zinc oxide for use in electrophotography.
  • Electrophotography is a wellknown process for converting a light image into .an electrostatic charge pattern on a sheet or support having an electrically insulating layer of material which is also photoconductive. In this process, a latent image is first produced, which can be developed into a visible image, resulting in reproduction of the original pattern.
  • a typical electrostatic reproduction process includes use of a recording member comprising a backing or support and bearing a layer or coating which normally is an insulator but which, on exposure to actinic radiation, becomes at least somewhat conductive.
  • An electrostatic charge is imparted to the backing and/or the surface of the photoconductive layer, establishing a potential between them.
  • a light image is then focused on the charged surface. The charge is dissipated in the exposed areas or partially dissipated depending on the amount of exposure, while the unexposed areas remain charged.
  • a pattern of electrostatic charges results which correspond to the light image.
  • the latent image may be rendered visible by applying thereto particles of charged electroscopic powder. The charged particles are held by electrostatic forces to charged areas of the sheet.
  • Electrostatic photography and electrostatic printing commonly use as a photosensitive element, a sheet of film, paper, or the like hearing a thin photoconductive insulating layer.
  • This layer includes not only photoconductive materials such as zinc oxide, but also includes a resin, such as an organic polymer, resin or natural rosin or the like for dark insulating purposes. These materials are applied by appropriate methods over a suitable base sheet.
  • the base sheet material is sometimes selected for its own electroconductive properties, in which case tlTe base normally will be connected to ground potential during the processing.
  • Highly conductive bases of this type have been prepared from sheet aluminum, carbon filled paper and the like.
  • it is possible to use relatively nonconductive base materials such as untreated paper or paper suitably filled or otherwise treated.
  • a charge in order to apply an electrostatic pattern, a charge must be imparted to the base material, which charge has a polarity different from or opposite to that to be applied on the photoconductive surface.
  • a sheet is coated with a layer of the photoconductive material, for example zinc oxide; the zinc oxide being supported in, mixed with, or covered by a resin or the like.
  • This layer normally provides an effective insulator so that a charge of one polarity may be imparted to the base sheet and a different charge which may be neutral or of opposite polarity is applied to the top of the resin film or photoconductive layer.
  • an electrostatic charge usually uniform over the whole area on the face of the photoconductive insulating layer by some suitable means 3,345,161 Patented Oct. 3, 1967 in the absence of actinic illumination.
  • the backing layer is either connected to ground or has applied thereto an approximately equivalent charge of opposite polarity.
  • the photoconductor is then illuminated by the light and shadow pattern which represents the image to be reproduced.
  • the necessary illumination for creating the latent image may be obtained in various ways, as by exposure to the output of an oscilloscope or equivalent, or exposure to a projector or camera or the like.
  • the hitherto insulating photoconductive material becomes electrically conductive or at least semi-conductive.
  • any previously deposited electrostatic surface charge is dissipated partly or entirely by this conductivity, generally according to the greater or lesser actinic exposure which each element of area has received.
  • the electrostatic latent image is formed with the greatest charge density remaining in the unexposed areas, and the least charged density remaining in those portions most highly illuminated.
  • the resulting latent image must be rendered visible by development which can be accomplished in several different ways.
  • electrostatically charged powdered particles of a pigment or so-called toners are applied to the latent image.
  • This application may be in the form of airborne clouds of pow der or the particles may be suspended in insulating liquids of relatively low dielectric properties. They also may be applied as dry particles adhering to oppositely charged carrier particles of substantially larger size. Carrier particles such as iron powder or very fine glass beads may be used for this purpose.
  • the electrostatic latent image and the development pigment or powder particles adhere differentially to charged, partially charged and discharged areas, thereby rendering them differentially visible.
  • the image is then in a typical xerographic operation, transferred by contact to a receiving sheet and is afiixed thereto.
  • the pigment may be directly aflixed to the photoconductive layer by drying to form a residue, by thermal fusion, or by the action of solvent vapor. The general details of this process are well known to those skilled in the art and need not be further elaborated here.
  • photoconductive materials which can be used in this general process.
  • materials such materials as the colored oxides, sulfides, selenides, tellurides and sometimes the iodides of various metals including cadmium, mercury, antimony, bismuth, thallium, indium, molybdenum, aluminum, lead, and zinc.
  • Certain other colored salts such as arsenic trisulfide, cadmium arsenide and lead chromate also have photoconductive properties.
  • the oxides of zinc are generally preferred for reasons of economy, because they respond well to electrostatic charges and they have a good wide range of light to dark conductivities, because they form a very useful white surface of good texture, and because they are widely available in suitable form.
  • Certain dyestuffs can be used with zinc oxide to increase its sensitivity to visible radiation. Those dyes which are capable of absorbing visible radiant energy and of transferring the absorbed energy to the zinc oxide itself, are most useful. A large number of dyestuffs have been suggested for this purpose but most of them have serious deficiencies. In the first place, the color of the Zinc oxide is white and it is not usually desirable to have this whiteness covered by deep colors.
  • zinc oxide is usually preferred as the pigment of the photoconductive insulator to be used in the production of electrophotographic images, as indicated above, it has certain deficiencies including a relatively insensitive to visible radiation.
  • the peak sensitivity of zinc oxide lies between 2,350 to about 3,900 Angstroms.
  • Various investigators have recognized that it is possible to sensitize zinc oxide to visible radiation by adsorbing suitable dyes upon its surface. This sort of sensitization renders the zinc oxide responsive to colored light and greatly increases its effective sensitivity to visible radiation.
  • the mechanism of optical sensitization is not yet clearly understood but it is believed that the sensitizer must be intimately associated and perhaps adsorbed directly on the crystal surface.
  • our novel process consists of heating the dry zinc oxide pigment with a suitable dye at a sufficiently elevated temperature and for a sufficient period of time to cause a surface reaction between the dye and the zinc oxide.
  • the temperature is preferably so high that the chemistry of the dye is somewhat altered. Hence, the reaction takes place between zinc oxide and an oxidation product or a residue of the dye rather than the dye itself.
  • the more common classes of sensitizing dyes can be used in this way.
  • Electrophotographic coatings were then made, using the treated zinc oxide, i.e., zinc oxide treated with dye at high temperature, and a resin emulsion of a water dispersible epoxy ester-vinyl acetate crotonic acid copolymer manufactured by Washburn & Co. under the trade name Xeroplex #1.
  • a clay-coated bond paper identified as .Crocker-Burbank T977, was coated with the zinc oxide and resin emulsion using a #18 wire-bound bar. Coatings were dried and the various samples were then tested in the manner next described.
  • a negative electrostatic charge was deposited upon the face of the photoconductive insulating layer of paper by means of a corona discharge device in the absence of actinic illumination.
  • the photoconductor was then illuminated in contact with a film positive, using a General Electric CDJ 100-watt tungsten light bulb mounted 30 inches above the image and operated at a color temperature of about 2950 F.
  • the latent image thus formed was rendered visible by a conventional positive blue liquid toner of the type described in US. Patent 2,907,674.
  • the sensitivity of the coating was determined by examining the resulting print for background toner pick-up, sharpness of image and image fill-in. The exposure time was adjusted by experiment to get a sharp image in each case. The results are summarized below:
  • This process causes the sensitizer apparently to form a less water-soluble material in conjunction with the zinc oxide. At the same time, the resulting product is not highly colored.
  • the coatings of undyed zinc oxide A and B showed normal behavior for an unsensitized electrophotographic coating.
  • Coating C was slightly sensitized in comparison to A and B, but was highly colored and was considered objectionable for this reason.
  • Coatings D, E and F showed an increase in sensitivity along with increased reductions of the original dye color. They also showed a reduction in dye solubility in the resin binder. It appears that optimum sensitization along with the desired White color is achieved best between the temperatures of steps F and G, which correspond to about the upper practical limit. Within this range, the required exposure for a good image was at a minimum, indicating maximum sensitization. At the same time, there was little or no background coloration.
  • the quantity of dye which is used to achieve sensitization may be as high as 0.5% based on the weight of the zinc oxide. It is preferred, however, to use lesser amounts and in many instances, it is advantageous to use the minimum amount which is capable of producing the desired results.
  • a range of 1 to parts per 1000 is considered to be the practical limit, although 1 to 2 parts per 1000 is most commonly preferred.
  • Patent Blue 600-670 5 Rose Bengal 550-600 5-7 Eosin 450-550 6-6 Erythrosin -7 Fluoreseein 450-550 6.
  • Patent Blue 600-670 5 Rose Bengal 550-600 5-7 Eosin 450-550 6-6 Erythrosin -7 Fluoreseein 450-550 6.
  • a sensitized photoconductive element comprising a base sheet coated with a photoconductive material preheated in dry form with a dyestufi' selected from the group consisting of acid dyes, basic dyes, anthraquinone 6 dyes and sulfonphthalein dyes, to a temperature frorr 400 to 650 F. sufficiently high to oxidize the dyestufl and react with said material whereby the coloring effect and aqueous resin emulsion solubility of said dyestutf is reduced.
  • a dyestufi' selected from the group consisting of acid dyes, basic dyes, anthraquinone 6 dyes and sulfonphthalein dyes
  • a process for the optical sensitization of white photoconductive materials normally insensitive to visible light radiation but sensitive to ultraviolet light comprises intimately mixing with said material, an organic dyestulf selected from the group consisting of acid dyes, basic dyes, anthraquinone dyes and sulfonphthalein dyes; heating the intimate mixture in dry form to a temperature from 400 to 650 F. suificiently high to permit an oxidation product of said dyestufi' to be formed and a reaction to occur between said material and said oxidized product thereby rendering the dyestuff less soluble in solvents; and dispersing the reacted material in an aqueous resin emulsion.
  • an organic dyestulf selected from the group consisting of acid dyes, basic dyes, anthraquinone dyes and sulfonphthalein dyes
  • a process according to claim 2, wherein the photoconductive material is zinc oxide.
  • the process of sensitizing zinc oxide to visible light radiation which comprises adding to zinc oxide a dye sensitizer selected from the group consisting of acid dyes, basic dyes, anthraquinone dyes and sulfonphthalein dyes, intimately mixing said zinc oxide and sensitizer and heating the mixture in dry form to a temperature ranging from 400 to 650 F. for at least 1 minute whereby said dye sensitizer is oxidized and reacted with said zinc oxide, the dye solubility in an aqueous resin emulsion, is reduced and the dye color is substantially destroyed to leave an essentially white product.
  • a dye sensitizer selected from the group consisting of acid dyes, basic dyes, anthraquinone dyes and sulfonphthalein dyes
  • the process of preparing a material useful in electrophotography which comprises coating a base with an aqueous resinous coating containing in suspension the reaction product of zinc oxide and an oxidized dyestuif selected from the group consisting of acid dyes, basic dyes, anthraquinone dyes and sulfonphthalein dyes, obtained by heating the zinc oxide and the dyestuff in dry form to an elevated temperature from 400 to 650 F. for a suflicient period of time to form an essentially water insoluble complex, drying the coating thus applied to deposit a resinous layer of the zinc oxide-dye complex on the base.
  • an oxidized dyestuif selected from the group consisting of acid dyes, basic dyes, anthraquinone dyes and sulfonphthalein dyes obtained by heating the zinc oxide and the dyestuff in dry form to an elevated temperature from 400 to 650 F. for a suflicient period of time to form an essentially water insoluble complex, drying the coating thus applied to deposit a

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)
US264759A 1963-03-13 1963-03-13 Photoconductive material and process for its preparation Expired - Lifetime US3345161A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US264759A US3345161A (en) 1963-03-13 1963-03-13 Photoconductive material and process for its preparation
GB7972/64A GB1033243A (en) 1963-03-13 1964-02-26 Photoconductive material and process for its preparation
DEG39993A DE1273324B (de) 1963-03-13 1964-03-03 Verfahren zur Empfindlichkeitssteigerung von Zinkoxyd
CH293964A CH440977A (de) 1963-03-13 1964-03-06 Verfahren zur optischen Sensibilisierung
FR967108A FR1385960A (fr) 1963-03-13 1964-03-12 Substance photoconductrice et procédé pour la préparer
NL6402707A NL6402707A (US20040242566A1-20041202-C00155.png) 1963-03-13 1964-03-13
BE645137D BE645137A (US20040242566A1-20041202-C00155.png) 1963-03-13 1964-03-13

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US264759A US3345161A (en) 1963-03-13 1963-03-13 Photoconductive material and process for its preparation

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US (1) US3345161A (US20040242566A1-20041202-C00155.png)
BE (1) BE645137A (US20040242566A1-20041202-C00155.png)
CH (1) CH440977A (US20040242566A1-20041202-C00155.png)
DE (1) DE1273324B (US20040242566A1-20041202-C00155.png)
GB (1) GB1033243A (US20040242566A1-20041202-C00155.png)
NL (1) NL6402707A (US20040242566A1-20041202-C00155.png)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3501330A (en) * 1964-10-26 1970-03-17 Agfa Gevaert Nv Manufacture of electrophotographic materials
US3506595A (en) * 1965-10-30 1970-04-14 Fuji Photo Film Co Ltd Photoconductive insulating material
US3507692A (en) * 1966-04-05 1970-04-21 Agfa Gevaert Nv Sensitization of photoconductive material
US3884688A (en) * 1966-05-16 1975-05-20 Xerox Corp Photosensitive element employing a vitreous bismuth-selenium film

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3051569A (en) * 1959-10-26 1962-08-28 American Photocopy Equip Co Photoconductive materials
US3052540A (en) * 1954-06-02 1962-09-04 Rca Corp Dye sensitization of electrophotographic materials
GB919684A (en) * 1960-06-01 1963-02-27 Agfa Ag The sensitisation of electrophotographic layers
US3121007A (en) * 1958-02-12 1964-02-11 Xerox Corp Photo-active member for xerography
US3128179A (en) * 1960-09-02 1964-04-07 Eastman Kodak Co Cyanine dye-sensitized photoconductive compositions comprising zinc oxide
US3203795A (en) * 1958-03-05 1965-08-31 Agfa Ag Photoconductive layers for electrophotography
US3238149A (en) * 1961-07-10 1966-03-01 Method for improxvlnxg the the photocondug thqe response of dye sensitized zinc ox de

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3052540A (en) * 1954-06-02 1962-09-04 Rca Corp Dye sensitization of electrophotographic materials
US3121007A (en) * 1958-02-12 1964-02-11 Xerox Corp Photo-active member for xerography
US3203795A (en) * 1958-03-05 1965-08-31 Agfa Ag Photoconductive layers for electrophotography
US3051569A (en) * 1959-10-26 1962-08-28 American Photocopy Equip Co Photoconductive materials
GB919684A (en) * 1960-06-01 1963-02-27 Agfa Ag The sensitisation of electrophotographic layers
US3128179A (en) * 1960-09-02 1964-04-07 Eastman Kodak Co Cyanine dye-sensitized photoconductive compositions comprising zinc oxide
US3238149A (en) * 1961-07-10 1966-03-01 Method for improxvlnxg the the photocondug thqe response of dye sensitized zinc ox de

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3501330A (en) * 1964-10-26 1970-03-17 Agfa Gevaert Nv Manufacture of electrophotographic materials
US3506595A (en) * 1965-10-30 1970-04-14 Fuji Photo Film Co Ltd Photoconductive insulating material
US3507692A (en) * 1966-04-05 1970-04-21 Agfa Gevaert Nv Sensitization of photoconductive material
US3884688A (en) * 1966-05-16 1975-05-20 Xerox Corp Photosensitive element employing a vitreous bismuth-selenium film

Also Published As

Publication number Publication date
GB1033243A (en) 1966-06-22
BE645137A (US20040242566A1-20041202-C00155.png) 1964-07-01
CH440977A (de) 1967-07-31
NL6402707A (US20040242566A1-20041202-C00155.png) 1964-09-14
DE1273324B (de) 1968-07-18

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Owner name: R Q O HOLDING COMPANY INC 111 WEST 2ND ST JAMESTOW

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Effective date: 19820526

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