US3637433A - Process for improving photoconductive elements - Google Patents

Process for improving photoconductive elements Download PDF

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Publication number
US3637433A
US3637433A US852018A US3637433DA US3637433A US 3637433 A US3637433 A US 3637433A US 852018 A US852018 A US 852018A US 3637433D A US3637433D A US 3637433DA US 3637433 A US3637433 A US 3637433A
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United States
Prior art keywords
insulating layer
photoconductive
photoconductive insulating
substrate
layer
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Expired - Lifetime
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US852018A
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English (en)
Inventor
Jimmy A Sims
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International Business Machines Corp
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International Business Machines Corp
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    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/07—Polymeric photoconductive materials
    • G03G5/071—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G5/072—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups
    • G03G5/073—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups comprising pending carbazole groups
    • 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
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0525—Coating methods

Definitions

  • I I l l I 1 element comprising a heat softenable PhOtOCOI'IdUCliVe lI'lSU- 96/13 96/18 lating layer on an electrically conductive substrate are im- 51 11111.0 ..B4 ld 1/18 Pwved by quickly heating the insulaing [58] Field orsein-cn ..117/201 34, 62; 96/l.5 abme flening Such as by PlaCing element in contact with a heated member for a short period of time.
  • Electrophotography utilizes the change in conductivity of photoconductive materials upon exposure to light.
  • a charge is placed on the surface of a photoconductive insulating layer and the surface is exposed imagewise to light.
  • the light discharges the surface areas which are struck by light with the charge usually being removed through an electrically conductive backing layer which may also serve as a support for the photoconductive insulating layer.
  • the areas which are not illuminated retain the charge and are developed, for example, by charged marking particles which are attracted to the image areas.
  • the quality of the developed image depends upon a number of factors.
  • One factor is the uniformity of the photoconductive insulating layer. Impurities in the layer can cause uneven charging of the layer and minute discontinuities in the layer can cause a shorting out of the charge to the conductive layer. The result is an imperfect electrical image and when the image is developed, parts of the image are missing and parts of the background areas which should remain blank are developed.
  • the nonuniformity of the surface of the photoconductive layer has been found to be a problem particularly with layers prepared by solvent coating techniques. Even when precise coating techniques are employed, discontinuities in the layer may occur. Another problem is the presence of traces of solvent which are difficult to remove by heating at times and temperatures at which the layer is stable. The residual solvent effects can be present either on the surface (blushing) and/or within the bulk of the film (solvent pockets) these effects cause nonuniform charging characteristics to the extent that unwanted development occurs around the areas of solvent concentration.
  • the properties of a photoconductive insulating layer are improved by heating the layer for a short time at a temperature above the softening point of the layer.
  • FIG. 1 is a schematic elevational side view with parts broken away of a system or apparatus for carrying out the process of the invention with the dimensions somewhat exaggerated for the purpose of illustration.
  • FIG. 2 is a schematic elevational side view of a system or apparatus for carrying out another embodiment of the process of the invention.
  • Suitable photoconductive materials for use in photoconductive insulating layers include, for example, both inorganic and organic compounds and various combinations thereof.
  • Representative compounds include, for example, selenium; cadmium sulfide, zinc sulfide; cadmium selenide; zinc oxide; anthracene, benzidine, oxazoles, triazines, pyrazolines, azomethines, anthraquinone, and polymers such as polyindene, polyacenaphthene polyvinylquinoline and polymers of n-vinyl carbazole and its lower alkyl and halogen derivatives. Mixtures of photoconductive compounds and polymers can be used.
  • Electron acceptors to increase the sensitivity or exposure speed can be added such as, for example, 2,4,7-tn'nitro-9- fluorenone; Q-(dicyanomethylene) 2,4,7-trinitrofluorene; phthalic anhydride; l,3,5-tricyanobenzine; l,5-diphenoxy anthraquinone; 2,3-dichloronaphthaquinone 1-4; and 3-nitro- N-butyl carbazole.
  • the materials themselves are film forming they may be coated from a solvent to form the photoconductive insulating layer.
  • the materials can be mixed with film forming insulating resins such as, for example, polyethylene, polystyrene, ethyl cellulose, polyacrylics and methacrylic acid esters, formaldehyde resins, polyethylene glycol esters, alkyd resins, polyurethane resins, silicon polymers and epoxy resins.
  • additives such as dyes which extend the spectral response of the photoconductor, or plasticizers and lubricants can be employed as is known in the art.
  • the materials making up the photoconductive layer are dissolved or dispersed in a volatile liquid carrier and then coated on a substrate, using conventional coating techniques, to a cured coating thickness usually of from about 5 to 50 microns.
  • Suitable solvents include, for example, toluene, xylene, petroleum ether, chlorobenzene, methyl ethyl ketone, tetrahydrofuran, benzene, 1,2-dichloro-ethene, ethanol, etc.
  • conductive substrates are used such as, for example, steel, aluminum, or plastic sheets such as, for example, as polyethylene and polyesters which have deposited thereon a conductive coating of aluminum, gold, or conductive particles dispersed in a binder.
  • the bulk of the liquid carrier is then removed by conventional techniques, for example, by passing the coated substrate into an air-circulating oven to dry the coating.
  • the treatment also eliminates discontinuities or pin holes" in the layer caused by improper coating or curing.
  • the heating can be of any convenient means to provide efiicient heat transfer to the photoconductive layer. It can be, for example, an infrared source, a heated surface such as a plate in stationary contact with the photoconductive element or it can be a moving surface such as a heated rotating cylindrical roll which is a convenient way to continuously treat long webs of material.
  • the element should be heated to a tem erature sufficient to soften the photoconductive layer to the point where the solvent can rapidly migrate through the layer to the atmosphere without causing damage to the substrate. Usually temperatures of from about 10 to C. above the softening point of the layers are adequate.
  • the heat source temperature required will vary depending upon the softening point of the binder phase of the photoconductive layer, the nature of the substrate, and the thickness of the photoconductive element.
  • the time of contact is short and usually less than 1 minute.
  • heating times of from about 1 to 10 seconds are employed depending upon the amount of solvent to be removed and the efficiency of heat transfer to the photoconductive layer.
  • Electrophotographic element 11 comprises a photoconductive insulating layer 13 which is about 18 microns in thickness and which comprises a 1:1 molar ratio of poly-N-vinylcarbazole and 2,4,7-trinitro-9- fluorenone.
  • the layer was prepared by roll coating a solvent solution of the two components of the layer onto a 3 mil aluminized Mylar polyester backing sheet 15 from the solvent, tetrahydrofuran. The layer was dried in an air-circulating oven at 100 C. for 2 minutes. After about 2 days observable solvent blemishes appeared on the surface of the layer.
  • the back surface 18 of sheet 15 of the left half of element 11 was placed in contact for about 2 seconds with an electrically heated platen 17 containing resistance wires 20 to heat stainless steel contacting plate 22 to a temperature of about 170 C.
  • the photoconductive insulating layer became heated to about 165 C. (The softening point of the continuous polyvinyl carbazole resin phase of the layer was about 100 C.)
  • the treated portion of element 11 quickly resolidified and had a surface which was smooth and glossy without any observable solvent defects.
  • the element 11 was secured to the surface of the cylindrical drum of a conventional electrophotographic copy apparatus and charged with a corona discharge to a negative polarity of about 600 volts, exposed imagewise to a line copy original for about 10 seconds, and cascade contacted with commercially available carrier and toner particles.
  • the toner particles were transferred and heat fused to a copy sheet.
  • the copy produced by the untreated portion of element 11 was relatively light with broken characters and background spots of toner. In contrast, the copy produced by the treated portion had darker images with sharp outlines and excellent character fill.
  • EXAMPLE II A portion of untreated photoconductive element prepared in the same manner as described in example I was placed in an air-circulating oven at an air temperature of 130 C. for 20 hours in an attempt to remove the residual solvent. Not only did the solvent defects persist, but the surface of the photoconductive layer became dull which was caused by crystallization of portions of the trinitrofluorenone. A portion of the surface of the backing sheet was placed in contact with plate 17 at a temperature of 165 C. for 3 seconds. The treated surface portion became smooth and glossy. The photoconductive layer when used in accordance with the procedure described in example 1 generated excellent copy for the treated portion and poor copy for the untreated portion.
  • FIG. 2 schematically shows another suitable system for treating the photoconductive insulating layer.
  • Element 21 has a photoconductive insulating layer 23 of 1 part by weight of copolymer of N-vinylcarbazole and ethylacrylate (41 mole percent N-vinylcarbazole) and 1.5 part by weight of 2,4,7- trinitro-9-fluorenone which layer was coated on a web of aluminized Mylar polyester 25 from a 1:1 volume ratio of methylene chloride and tetrachloroethane carrier liquid.
  • the surface of the moving element was transported from supply spool 24 to a driven takeup spool 26 past treating station 28 where sheet 25 was contacted by a driven rotating steel roll 27 whose surface was heated at a temperature of about 160C.
  • the speed of the roll was adjusted to approximately equal the speed of the element to maximize the heat transfer to element 21.
  • the speed was adjusted so that the residence time of each portion of element 21 in contact with the surface of the roll 27 was about seconds.
  • the layer 23 quickly cooled and solidified under ambient conditions after leaving roll 27 without need to provide any special cooling means. Portions of the heated web were used in an electrophotographic copy machine to produce images which when transferred and fused to plain paper showed sharp outlines, with good character fill, and no background toner caused by residual solvent effects.
  • a method of improving the properties of a photoconductive insulating layer comprising heating said layer from about 10 to about 70 C. above the softening point for a short time, sufficient to evaporate residual solvent from said insulating layer.
  • a method of improving the properties of a photoconductive element comprising a photoconductive insulating layer supported on a conductive substrate which method comprises heating said element from about 10 to about 70 C. above the softening point of said photoconductive insulating layer for a short period of time, sufficient to evaporate residual solvent from said insulating layer.
  • heating is accomplished by placing said substrate in contact with a plate.
  • a process for improving the properties of a photoconductive element comprising a heat softenable photoconductive insulating layer supported on a substrate, said element having been prepared by coating said substrate with a solvent mixture of the material comprising said layer and evaporating the bulk of said solvent, said process comprising the steps of applying heat to the surface of said substrate opposite said photoconductive insulating layer at a temperature less than about 70 C. above the softening point of said photoconductive insulating layer so as to permit rapid escape of solvent from said layer, continuing said heating for a time sufficient to evaporate the residual solvent from said photoconductive insulating layer, and then cooling said element to resolidify said photoconductive insulating layer.
  • a process for improving the properties of a photoconductive element comprising a heat softenable photoconductive insulating layer supported on an electrically conductive substrate, said element having been prepared by coating said substrate with a solvent mixture comprising poly-N-vinyl carbazole and 2,4,7-trinitro-9-fluorenone in tetrahydrofuran and evaporating the bulk of said tetrahydrofuran, said method comprising the steps of applying heat to the surface of said substrate opposite said photoconductive insulating layer to heat said insulating layer to a temperature of from about to C. to soften said photoconductive insulating layer so as to permit rapid escape of solvent from said layer, continuing said heating for from 1 to 10 seconds to evaporate the residual solvent from said photoconductive insulating layer, and then cooling said element to resolidify said photoconductive insulating layer.
  • a process for improving the properties of a photoconductive element comprising a heat softenable photoconductive insulating layer supported on an electrically conductive substrate, said element having been prepared by coating said substrate with a solvent mixture comprising a copolymer of N- vinyl carbazole and ethylacrylate and 2,4,7-trinitro-9- fluorenone in methylene chloride and tetrachloroethane and evaporating the bulk of said methylene chloride and tetrachloroethane, said method comprising the steps of applying heat to the surface of said substrate opposite said photoconductive insulating layer to a temperature of about 160 C.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Photoreceptors In Electrophotography (AREA)
US852018A 1969-08-21 1969-08-21 Process for improving photoconductive elements Expired - Lifetime US3637433A (en)

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US85201869A 1969-08-21 1969-08-21

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US (1) US3637433A (enrdf_load_stackoverflow)
JP (1) JPS5419784B1 (enrdf_load_stackoverflow)
CA (1) CA941661A (enrdf_load_stackoverflow)
DE (1) DE2039484C3 (enrdf_load_stackoverflow)
FR (1) FR2057768A5 (enrdf_load_stackoverflow)
GB (1) GB1264082A (enrdf_load_stackoverflow)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3966469A (en) * 1973-09-14 1976-06-29 Matsushita Electric Industrial Co., Ltd. Electrophotographic photosensitive composition employing a prepolymer of diallylphthalate
US4117072A (en) * 1974-10-16 1978-09-26 Xerox Corporation Process for enhancement of mechanical properties of photoconductive polymers
US4252883A (en) * 1972-04-28 1981-02-24 Canon Kabushiki Kaisha Process for producing electrophotographic photosensitive member
US4497566A (en) * 1983-03-03 1985-02-05 Eastman Kodak Company Correction of image defects in photoconductive film
US6300029B1 (en) * 1999-03-02 2001-10-09 Ricoh Company, Ltd. Electrophotographic image forming process and electrophotographic photoconductor
US20050005794A1 (en) * 2003-06-05 2005-01-13 Fuji Photo Film Co., Ltd. Coating method and planographic printing plate

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5128229A (en) * 1989-09-27 1992-07-07 Mita Industrial Co., Ltd. Electrophotosensitive material and method of manufacturing the same
US5162183A (en) * 1990-07-31 1992-11-10 Xerox Corporation Overcoat for imaging members

Citations (1)

* 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

Patent Citations (1)

* 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

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4252883A (en) * 1972-04-28 1981-02-24 Canon Kabushiki Kaisha Process for producing electrophotographic photosensitive member
US3966469A (en) * 1973-09-14 1976-06-29 Matsushita Electric Industrial Co., Ltd. Electrophotographic photosensitive composition employing a prepolymer of diallylphthalate
US4117072A (en) * 1974-10-16 1978-09-26 Xerox Corporation Process for enhancement of mechanical properties of photoconductive polymers
US4497566A (en) * 1983-03-03 1985-02-05 Eastman Kodak Company Correction of image defects in photoconductive film
US6300029B1 (en) * 1999-03-02 2001-10-09 Ricoh Company, Ltd. Electrophotographic image forming process and electrophotographic photoconductor
US20050005794A1 (en) * 2003-06-05 2005-01-13 Fuji Photo Film Co., Ltd. Coating method and planographic printing plate

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Publication number Publication date
DE2039484B2 (de) 1978-08-31
DE2039484C3 (de) 1979-04-26
JPS5419784B1 (enrdf_load_stackoverflow) 1979-07-18
CA941661A (en) 1974-02-12
FR2057768A5 (enrdf_load_stackoverflow) 1971-05-21
DE2039484A1 (de) 1971-03-04
GB1264082A (enrdf_load_stackoverflow) 1972-02-16

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