EP0690350B1 - Organic photoconductor - Google Patents
Organic photoconductor Download PDFInfo
- Publication number
- EP0690350B1 EP0690350B1 EP95202276A EP95202276A EP0690350B1 EP 0690350 B1 EP0690350 B1 EP 0690350B1 EP 95202276 A EP95202276 A EP 95202276A EP 95202276 A EP95202276 A EP 95202276A EP 0690350 B1 EP0690350 B1 EP 0690350B1
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- EP
- European Patent Office
- Prior art keywords
- charge transport
- transport layer
- photoconductor
- layer
- solvent
- Prior art date
- 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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Classifications
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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
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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
- G03G5/005—Materials for treating the recording members, e.g. for cleaning, reactivating, polishing
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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
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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
- G03G5/10—Bases for charge-receiving or other layers
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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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/147—Cover layers
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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
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/147—Cover layers
- G03G5/14708—Cover layers comprising organic material
- G03G5/14713—Macromolecular material
- G03G5/14747—Macromolecular material obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/1476—Other polycondensates comprising oxygen atoms in the main chain; Phenol resins
Definitions
- the present invention relates to a method of reducing stress related cracking in a photoconductor when the photoconductor is subjected to mechanical stress and used in a liquid toner imaging machine as defined in claim 1 and to an inorganic photoconductor obtainable by this method as defined in claim 10 organic photoconductors.
- organic photoconductors are known. Most organic photoconductors are susceptible to attack by organic solvents of the type used in liquid toner electrophotography and are therefore unsuitable for such applications. These photoconductors include those which dissolve in the solvents and others which are caused to crack as the result of exposure thereto when they are under stress, especially when under tension.
- the present invention seeks to provide an improved organic photoconductor which is resistant to cracking in a stressed environment wherein organic solvents of the type used in liquid toner electrophotography are present.
- the first material is relatively more flexible than the second material.
- the first material is relatively flexible less flexible and stretchable material, which has been chemically treated to increase its stretchability and flexibility.
- an organic photoconductor including a base layer formed on a first material and a photoconductive layer formed of a second material, the second material being chemically treated to relieve stress therein.
- the chemical treatment causes the charge transport layer to become more flexible ans stretchable.
- the charge transport layer becomes more elastic or plastic.
- the base layer of the organic photoconductor has greater flexibility and stretchability than the photoconductor layer.
- the base layer has a stress relief temperature higher than that of the photoconductive layer.
- the step of treating includes the step of chemically treating the photoconductive layer to soften and render it more elastic or plastic that it previously was.
- liquid toner electrophotographic apparatus as claimed in claim 11.
- the photoconductor sheet is constructed and operative in accordance with any of the embodiments described above, alone or in suitable combination.
- FIG. 1 illustrates liquid toner electrophotographic imaging apparatus constructed and operative in accordance with the present invention.
- the invention is described for liquid developer systems with negatively charged toner particles, and negatively charged photoconductors, i.e., systems operating in the reversal mode.
- toner particle and photoconductor polarity the values and polarities of the voltages are changed, in accordance with the principle of the invention.
- the invention can be practiced using a variety of liquid developer types but is especially useful for liquid developers comprising carrier liquid and pigmented polymeric toner particles.
- the carrier liquid is a solvent such as Isopar (Exxon). Examples of such developers are given in U. S. Patent 4,794,651, the disclosure of which is included herein by reference.
- the apparatus of Fig. 1 typically comprises a drum 10 arranged for rotation about an axle 12 in a direction generally indicated by arrow 14.
- An organic photoconductor 100 is mounted on the drum and is stretched tight by stretchers 99.
- a corona discharge device 18 is operative to generally uniformly charge organic photoconductor 100 with a negative charge.
- the latent image comprises image areas at a given range of potentials and background areas at a different potential.
- the image may be laser generated as in printing from a computer or it may be the image of an original as in a copier.
- Development unit 22 is operative to apply liquid developer, comprising a solids portion including pigmented toner particles and a liquid portion including carrier liquid preferably an organic liquid, to develop the electrostatic latent image.
- the developed image includes image areas having pigmented toner particles thereon and background areas.
- development unit 22 is shown as a single color developer of a conventional type, it may be replaced by a plurality of single color developers for the production of full color images as is known in the art.
- full color images may be produced by changing the liquid toner in the development unit when the color to be printed is changed.
- highlight color development may be employed, as is known in the art.
- photoconductor 100 passes a typically charged rotating roller 26, preferably rotating in a direction indicated by an arrow 28.
- roller 26 typically acts as a metering roller as is known in the art, reducing the amount of carrier liquid on the background areas and reducing the amount of liquid overlaying the image.
- roller 26 is intermediate that of the latent image areas and of the background areas on the photoconductor.
- Typical approximate voltages are: roller 26: -200 V to -800 V, background area: -1000 V and latent image areas: -150 V.
- the liquid toner image which passes roller 26 should be relatively free of pigmented particles except in the region of the latent image.
- Rigidizing roller 30 is preferably formed of resilient polymeric material, such as polyurethane which may have only its natural conductivity or which may be filled with carbon black to increase its conductivity.
- roller 30 is urged against photoconductor 100 as by a spring mounting (not shown).
- the surface of roller 30 typically moves in the same direction and with the same velocity as the photoconductor surface to remove liquid from the image.
- roller 30 is biased to a potential of at least several hundred and up to several thousand Volts with respect to the potential of the developed image on photoconductor 100, so that it repels the charged pigmented particles and causes them to more closely approach the image areas of photoconductor 100, thus compacting and rigidizing the image.
- rigidizing roller 30 comprises an aluminum core having a 20 mm diameter, coated with a 4 mm thick carbon-filled polyurethane coating having a Shore A hardness of about 30-35, and a volume resistivity of about 10 8 ohm-cm.
- roller 30 is urged against photoconductor 100 with a pressure of about 40-70 grams per linear cm of contact, which extends along the length of the drum.
- the core of rigidizing roller 30 is energized to between about -1800 and -2800 volts, to provide a voltage difference of preferably between about 1600 and 2700 volts between the core and the photoconductor surface in the image areas.
- the solids percentage in the image portion is believed to be as high as 35% or more. It is preferable to have an image with at least 25-30% solids, after rigidizing.
- apparatus for direct transfer of the image from organic photoconductor 100 to a substrate 130 such as paper Downstream of rigidizing roller 30 there is provided apparatus for direct transfer of the image from organic photoconductor 100 to a substrate 130 such as paper.
- the direct transfer is effected by the provision of guide rollers 132, 134 and 136, which guide a continuous web of substrate 130, and a drive roller 138, which cooperates with a support web 140.
- a suitable charging device such as corona discharge device 142, charges the substrate at a transfer location, for effecting electrophoretic transfer of the image from photoconductor 100 to substrate 130.
- photoconductor 100 is engaged by a cleaning roller 50, which typically rotates in a direction indicated by an arrow 52, such that its surface moves in a direction opposite to the movement of adjacent surface of photoconductor 100 which it operatively engages.
- Cleaning roller 50 is operative to scrub and clean photoconductor 100.
- a cleaning material such as toner or another cleaning solvent, may be supplied to the cleaning roller 50, via a conduit 54.
- a wiper blade 56 completes the cleaning of the photoconductor surface. Any residual charge left on photoconductor 100 is removed by flooding the photoconductor surface with light from a lamp 58.
- the direct transfer apparatus may be replaced by an intermediate transfer member which receives the images from photoconductor 100 and transfers them to the final substrate.
- Fig. 2 illustrates an organic photoconductor sheet 100, used in the apparatus of Fig. 1.
- the sheet comprises a base layer 102, typically formed of Aluminized Polyethylene Telephthalate, which is commercially available under the trademark Mylar.
- the base layer is preferably about 80 ⁇ m (microns) in thickness and has a melting point of 250°C.
- a sublayer 104 Disposed above the base layer 102 is a sublayer 104, typically formed of Polyester, Toluenesulfonamide-formaldehyde resin and a Polyamide and having a thickness of about 0.2 ⁇ m (microns).
- a charge generation layer 106 Disposed above the sublayer 104 is a charge generation layer 106, typically formed of Hydroxysquarylium Dye and Toluenesulfonamide-resin and having a thickness of about 0.3 ⁇ m (microns).
- a charge transport layer 108 Disposed above layer 106 is a charge transport layer 108, typically formed of Polyester, Polycarbonate, Yellow Dye, 4-[N,N-diethylamino] benzaldehydedipenylhydrazone and Polysiloxane in a minor proportion, having a thickness of about 18 ⁇ m (microns).
- Charge transport layer 108 and charge generation layer 106 together define the photoconductive layer referred to above.
- organic photoconductor 100 is treated chemically to reduce stress cracking in a liquid toner environment.
- the charge transport layer is treated with a solvent or other reagent to soften charge transport layer 108 end to render it more stretchable, i.e., more plastic or elastic than it was previously.
- the chemical treatment is selected so as to leave the electrical and optical characteristics of the photoconductor essentially unchanged.
- a chemically treated treated photoconductor sheet is stretched around drum 10, stress does not develop in charge transport layer 108. Accordingly, when stretched photoconductor 100 is exposed to organic solvents it does not tend to crack.
- a specific chemical treatment which has been found to be effective is dipping of photoconductor 100 in cyclohexanone diluted by isopropyl alcohol in the ratio 1:5 for 2 minutes. This treatment does not significantly change the electrical and optical characteristics of the photoconductor but eliminates cracking as described above.
- An alternative chemical treatment employs cyclohexanone alone or vinyl modified epoxy 1A24, commercially available from HumiSeal Division of Columbia Chase Corporation of Woodside, NY, diluted 1:20 with cyclohexanone. These materials can be applied by a wire-rod technique on the top surface of photoconductor 100.
- an RK Print-Coat Instrument Ltd. of Litlington, Royston, Merts., UK, Model KCC 303 coater, using bar #2 (rod diameter 13 mm, wire diameter 0.15 mm) may be operated with bar linear speed of 70 mm/sec.
- the residual vinyl modified epoxy forms a mechanically protective overcoating which is substantially abhesive to toner particles after the evaporation of the solvent.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Liquid Developers In Electrophotography (AREA)
- Light Receiving Elements (AREA)
Description
- The present invention relates to a method of reducing stress related cracking in a photoconductor when the photoconductor is subjected to mechanical stress and used in a liquid toner imaging machine as defined in claim 1 and to an inorganic photoconductor obtainable by this method as defined in
claim 10 organic photoconductors. - Various types of organic photoconductors are known. Most organic photoconductors are susceptible to attack by organic solvents of the type used in liquid toner electrophotography and are therefore unsuitable for such applications. These photoconductors include those which dissolve in the solvents and others which are caused to crack as the result of exposure thereto when they are under stress, especially when under tension.
- It is known in the art to provide protectrice coatings for organic photoconductors. Examples of these coatings are given in U.S. Patents 4,891,290 and 4,894,304.
- The present invention seeks to provide an improved organic photoconductor which is resistant to cracking in a stressed environment wherein organic solvents of the type used in liquid toner electrophotography are present.
- There is thus in accordance with the present invention a method of reducing stress related cracking in a photoconductor when the photoconductor is subjected to mechanical stress and used in a liquid toner imaging machine as defined in claim 1 and to an inorganic photoconductor obtainable by this method as defined in
claim 10. It also provides an organic photoconductor including a base layer formed of a first material and a photoconductive layer formed of a second material comprising a charge generating layer and a charge transport layer, the organic photoconductor being characterized in that when it is maintained in a curved orientation with the photoconductive layer facing outward, the photoconductive layer is subjected to less stress than the base layer. In accordance with a preferred embodiment of the invention the first material is relatively more flexible than the second material. In accordance with an alternative preferred embodiment of the invention the first material is relatively flexible less flexible and stretchable material, which has been chemically treated to increase its stretchability and flexibility. - There is further provided in accordance with the present invention an organic photoconductor including a base layer formed on a first material and a photoconductive layer formed of a second material, the second material being chemically treated to relieve stress therein. In the invention, the chemical treatment causes the charge transport layer to become more flexible ans stretchable. Preferably the charge transport layer becomes more elastic or plastic.
- Additionally in accordance with the present invention there is provided a method of reducing stress related cracking in an organic photoconductor as defined in claim 1.
- Additionally in accordance with the above embodiment of the invention, the base layer of the organic photoconductor has greater flexibility and stretchability than the photoconductor layer.
- Further in accordance with the above embodiment of the invention, the base layer has a stress relief temperature higher than that of the photoconductive layer.
- In accordance with the invention, the step of treating includes the step of chemically treating the photoconductive layer to soften and render it more elastic or plastic that it previously was.
- Additionally in accordance with the invention there is provided a liquid toner electrophotographic apparatus as claimed in claim 11.
- In accordance with a preferred embodiment of the invention, the photoconductor sheet is constructed and operative in accordance with any of the embodiments described above, alone or in suitable combination.
- The present invention will be understood and appreciated more fully from the following detailed description, taken in conjunction with the drawings in which:
- Fig. 1 is a simplified sectional illustration of liquid toner electrophotographic apparatus constructed and operative in accordance with the present invention; and
- Fig. 2 is a simplified illustration of an organic photoconductor sheet used in the apparatus of Fig. 1.
- Reference is now made to Fig. 1 which illustrates liquid toner electrophotographic imaging apparatus constructed and operative in accordance with the present invention. The invention is described for liquid developer systems with negatively charged toner particles, and negatively charged photoconductors, i.e., systems operating in the reversal mode. For other combinations of toner particle and photoconductor polarity, the values and polarities of the voltages are changed, in accordance with the principle of the invention.
- The invention can be practiced using a variety of liquid developer types but is especially useful for liquid developers comprising carrier liquid and pigmented polymeric toner particles. In a preferred embodiment of the invention the carrier liquid is a solvent such as Isopar (Exxon). Examples of such developers are given in U. S. Patent 4,794,651, the disclosure of which is included herein by reference.
- As in conventional electrophotographic systems, the apparatus of Fig. 1 typically comprises a
drum 10 arranged for rotation about anaxle 12 in a direction generally indicated byarrow 14. Anorganic photoconductor 100 is mounted on the drum and is stretched tight bystretchers 99. - A
corona discharge device 18 is operative to generally uniformly chargeorganic photoconductor 100 with a negative charge. Continued rotation ofdrum 10 brings chargedorganic photoconductor 100 into image receiving relationship with an exposure unit including alens 20, which focuses an image onto chargedorganic photoconductor 100, selectively discharging the photoconductor, thus producing an electrostatic latent image thereon. The latent image comprises image areas at a given range of potentials and background areas at a different potential. The image may be laser generated as in printing from a computer or it may be the image of an original as in a copier. - Continued rotation of
drum 10 bringscharged photoconductor 100, bearing the electrostatic latent image, into adevelopment unit 22 including chargeddeveloper plates 24.Development unit 22 is operative to apply liquid developer, comprising a solids portion including pigmented toner particles and a liquid portion including carrier liquid preferably an organic liquid, to develop the electrostatic latent image. The developed image includes image areas having pigmented toner particles thereon and background areas. - While
development unit 22 is shown as a single color developer of a conventional type, it may be replaced by a plurality of single color developers for the production of full color images as is known in the art. Alternatively, full color images may be produced by changing the liquid toner in the development unit when the color to be printed is changed. Alternatively, highlight color development may be employed, as is known in the art. - In accordance with a preferred embodiment of the invention, following application of toner thereto,
photoconductor 100 passes a typically charged rotatingroller 26, preferably rotating in a direction indicated by anarrow 28. Typically the spatial separation ofroller 26 fromphotoconductor 100 is about 50 microns.Roller 26 thus acts as a metering roller as is known in the art, reducing the amount of carrier liquid on the background areas and reducing the amount of liquid overlaying the image. - Preferably the potential on
roller 26 is intermediate that of the latent image areas and of the background areas on the photoconductor. Typical approximate voltages are: roller 26: -200 V to -800 V, background area: -1000 V and latent image areas: -150 V. - The liquid toner image which passes
roller 26 should be relatively free of pigmented particles except in the region of the latent image. - Downstream of
roller 26 there is preferably provided a rigidizingroller 30. Rigidizingroller 30 is preferably formed of resilient polymeric material, such as polyurethane which may have only its natural conductivity or which may be filled with carbon black to increase its conductivity. - According to one embodiment of the invention,
roller 30 is urged againstphotoconductor 100 as by a spring mounting (not shown). The surface ofroller 30 typically moves in the same direction and with the same velocity as the photoconductor surface to remove liquid from the image. - Preferably, the biased squeegee described in U. S. Patent 4,286,039, the disclosure of which is incorporated herein by reference, is used as the
roller 30.Roller 30 is biased to a potential of at least several hundred and up to several thousand Volts with respect to the potential of the developed image onphotoconductor 100, so that it repels the charged pigmented particles and causes them to more closely approach the image areas ofphotoconductor 100, thus compacting and rigidizing the image. - In a preferred embodiment of the invention, rigidizing
roller 30 comprises an aluminum core having a 20 mm diameter, coated with a 4 mm thick carbon-filled polyurethane coating having a Shore A hardness of about 30-35, and a volume resistivity of about 108 ohm-cm. Preferablyroller 30 is urged againstphotoconductor 100 with a pressure of about 40-70 grams per linear cm of contact, which extends along the length of the drum. The core of rigidizingroller 30 is energized to between about -1800 and -2800 volts, to provide a voltage difference of preferably between about 1600 and 2700 volts between the core and the photoconductor surface in the image areas. - Under these conditions and for the preferred toner, the solids percentage in the image portion is believed to be as high as 35% or more. It is preferable to have an image with at least 25-30% solids, after rigidizing.
- Downstream of rigidizing
roller 30 there is provided apparatus for direct transfer of the image fromorganic photoconductor 100 to asubstrate 130 such as paper. The direct transfer is effected by the provision of 132, 134 and 136, which guide a continuous web ofguide rollers substrate 130, and adrive roller 138, which cooperates with asupport web 140. A suitable charging device, such ascorona discharge device 142, charges the substrate at a transfer location, for effecting electrophoretic transfer of the image fromphotoconductor 100 tosubstrate 130. - Following transfer of the toner image to
substrate 130,photoconductor 100 is engaged by a cleaningroller 50, which typically rotates in a direction indicated by anarrow 52, such that its surface moves in a direction opposite to the movement of adjacent surface ofphotoconductor 100 which it operatively engages.Cleaning roller 50 is operative to scrub andclean photoconductor 100. A cleaning material, such as toner or another cleaning solvent, may be supplied to the cleaningroller 50, via aconduit 54. Awiper blade 56 completes the cleaning of the photoconductor surface. Any residual charge left onphotoconductor 100 is removed by flooding the photoconductor surface with light from alamp 58. - In a multi-color system, subsequent to completion of the cycle for one color the cycle is sequentially repeated for other colors which are sequentially transferred from
photoconductor 100 tosubstrate 130. - Alternatively the direct transfer apparatus may be replaced by an intermediate transfer member which receives the images from
photoconductor 100 and transfers them to the final substrate. - Fig. 2 illustrates an
organic photoconductor sheet 100, used in the apparatus of Fig. 1. The sheet comprises abase layer 102, typically formed of Aluminized Polyethylene Telephthalate, which is commercially available under the trademark Mylar. The base layer is preferably about 80 µm (microns) in thickness and has a melting point of 250°C. - Disposed above the
base layer 102 is asublayer 104, typically formed of Polyester, Toluenesulfonamide-formaldehyde resin and a Polyamide and having a thickness of about 0.2 µm (microns). Disposed above thesublayer 104 is acharge generation layer 106, typically formed of Hydroxysquarylium Dye and Toluenesulfonamide-resin and having a thickness of about 0.3 µm (microns). - Disposed above
layer 106 is acharge transport layer 108, typically formed of Polyester, Polycarbonate, Yellow Dye, 4-[N,N-diethylamino] benzaldehydedipenylhydrazone and Polysiloxane in a minor proportion, having a thickness of about 18 µm (microns).Charge transport layer 108 andcharge generation layer 106 together define the photoconductive layer referred to above. - The organic photoconductor described so far is commercially available from IBM Corporation under the trade name Emerald.
- In accordance with the present invention,
organic photoconductor 100 is treated chemically to reduce stress cracking in a liquid toner environment. The charge transport layer is treated with a solvent or other reagent to softencharge transport layer 108 end to render it more stretchable, i.e., more plastic or elastic than it was previously. - The chemical treatment is selected so as to leave the electrical and optical characteristics of the photoconductor essentially unchanged. When such a chemically treated treated photoconductor sheet is stretched around
drum 10, stress does not develop incharge transport layer 108. Accordingly, when stretchedphotoconductor 100 is exposed to organic solvents it does not tend to crack. - A specific chemical treatment which has been found to be effective is dipping of
photoconductor 100 in cyclohexanone diluted by isopropyl alcohol in the ratio 1:5 for 2 minutes. This treatment does not significantly change the electrical and optical characteristics of the photoconductor but eliminates cracking as described above. - An alternative chemical treatment employs cyclohexanone alone or vinyl modified epoxy 1A24, commercially available from HumiSeal Division of Columbia Chase Corporation of Woodside, NY, diluted 1:20 with cyclohexanone. These materials can be applied by a wire-rod technique on the top surface of
photoconductor 100. In such a case, an RK Print-Coat Instrument Ltd. of Litlington, Royston, Merts., UK, Model KCC 303 coater, using bar #2 (rod diameter 13 mm, wire diameter 0.15 mm) may be operated with bar linear speed of 70 mm/sec. - If pure cyclohexanone is used, then the results are similar to those for dipping, and the solvent evaporates within about 20-30 seconds.
- If the mixture of cyclohexanone and epoxy is used, then in addition to the above described effects of the cyclohexanone, the residual vinyl modified epoxy forms a mechanically protective overcoating which is substantially abhesive to toner particles after the evaporation of the solvent.
- It will be appreciated by persons skilled in the art that the present invention is not limited by what has been particularly shown and described hereinabove. Rather the scope of the present invention is defined only by the appended claims.
Claims (11)
- A method of reducing stress related cracking in an organic photoconductor, when the photoconductor is subjected to mechanical stress and used in a liquid toner imaging machine, including the steps of:providing an organic photoconductor (100) having a base layer (102) and a photoconductive layer formed of a charge generating layer (106) and a charge transport layer (108); andchemically treating the charge transport layer (108) in the provided organic photoconductor by contacting it with a solvent or other reagent to soften the charge transport layer and make it more stretchable to reduce stress related cracking in the charge transport layer, without substantially changing the optical and electrical characteristics of the photoconductor.
- A method according to claim 1 wherein the base layer of the provided organic photoconductor has greater flexibility and stretchability than the charge transport layer
- A method according to claim 1 or claim 2 wherein the step of chemically treating includes rendering the charge transport layer more elastic than it previously was.
- A method according to any of the preceding claims wherein the step of treating includes rendering the charge transport layer more plastic than it previously was.
- A method according to claim 3 or claim 4 wherein the step of chemically treating also includes forming a mechanically protective layer on the charge transport layer.
- A method according to claim 5 wherein said protective material is an vinyl modified epoxy.
- A method according to any of the preceding claims, wherein said step of chemically treating comprises the step of applying an organic solvent to the charge transport layer.
- A method according to any of claims 1-6 wherein said step of chemically treating comprises the steps of:applying of a protective material in an organic solvent to the charge transport layer whereby said solvent causes said charge transport layer to soften and become more-stretchable; andallowing the solvent to evaporate to leave a protective coating on the charge transport layer.
- A method according to claim 7 or claim 8 wherein said solvent is cyclohexanone.
- An organic photoconductor (100) having a base layer (102) and a photoconductive layer formed of a charge generating layer (106) and a charge transport layer (108) and being obtainable according to the method of any one of the preceding claims.
- A liquid toner electrophotographic apparatus comprising:a drum (10);an organic photoconductor according to claim 10 disposed on the surface of the drum; means for forming a latent image on the charge transport surface;means for liquid toner development of the latent image on the charge transport surface andmeans for transferring the image after development thereof to a final substrate.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1990634235 DE69034235T2 (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
| EP95202276A EP0690350B1 (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/NL1990/000066 WO1991017485A1 (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
| EP95202276A EP0690350B1 (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
| CA002082416A CA2082416C (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
| EP90908309A EP0527727B1 (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP90908309A Division EP0527727B1 (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
| EP90908309.9 Division | 1990-05-08 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP0690350A2 EP0690350A2 (en) | 1996-01-03 |
| EP0690350A3 EP0690350A3 (en) | 1996-07-03 |
| EP0690350B1 true EP0690350B1 (en) | 2007-01-24 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP95202276A Expired - Lifetime EP0690350B1 (en) | 1990-05-08 | 1990-05-08 | Organic photoconductor |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP0690350B1 (en) |
| WO (1) | WO1991017485A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5167987A (en) | 1991-11-04 | 1992-12-01 | Xerox Corporation | Process for fabricating electrostatographic imaging members |
| JP3318373B2 (en) * | 1991-12-23 | 2002-08-26 | ゼロックス・コーポレーション | Method of manufacturing flexible electrophotographic imaging member |
| US5532103A (en) * | 1992-08-19 | 1996-07-02 | Xerox Corporation | Multilayer electrophotographic imaging member |
| US5476740A (en) * | 1992-08-19 | 1995-12-19 | Xerox Corporation | Multilayer electrophotographic imaging member |
| US5508790A (en) * | 1994-09-07 | 1996-04-16 | Indigo N.V. | Photoreceptor sheet and imaging system utilizing same |
| IL117950A (en) * | 1996-04-17 | 2004-09-27 | Hewlett Packard Indigo Bv | Imaging apparatus and photoreceptor therefor |
| DE69705328T2 (en) * | 1997-03-13 | 2002-01-03 | Indigo N.V., Maastricht | ORGANIC PHOTOGRAPHER AND ITS TREATMENT |
| US20040197689A1 (en) * | 2001-08-30 | 2004-10-07 | Benzion Landa | Scratch resistant organic photoreceptor |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1814644B2 (en) * | 1967-12-26 | 1976-09-02 | Fuji Shashin Film K.K., Ashigara, Kanagawa (Japan) | ELECTROPHOTOGRAPHIC RECORDING MATERIAL |
| DE1906969A1 (en) * | 1969-02-07 | 1970-08-20 | Matsushita Electric Ind Co Ltd | Flexible, transparent electrophotographic - recording material |
| US3717462A (en) * | 1969-07-28 | 1973-02-20 | Canon Kk | Heat treatment of an electrophotographic photosensitive member |
| US3764590A (en) * | 1970-04-08 | 1973-10-09 | Hitachi Ltd | Organic photoconductive materials |
| JPS4923905B1 (en) * | 1970-10-31 | 1974-06-19 | ||
| US4286039A (en) | 1979-05-15 | 1981-08-25 | Savin Corporation | Method and apparatus for removing excess developing liquid from photoconductive surfaces |
| DE3032773A1 (en) * | 1980-08-30 | 1982-05-06 | Hoechst Ag, 6000 Frankfurt | ELECTROPHOTOGRAPHIC RECORDING MATERIAL AND METHOD FOR THE PRODUCTION THEREOF |
| US4497566A (en) * | 1983-03-03 | 1985-02-05 | Eastman Kodak Company | Correction of image defects in photoconductive film |
| US4794651A (en) | 1984-12-10 | 1988-12-27 | Savin Corporation | Toner for use in compositions for developing latent electrostatic images, method of making the same, and liquid composition using the improved toner |
| JPH0792610B2 (en) | 1987-06-10 | 1995-10-09 | 富士電機株式会社 | Electrophotographic photoconductor |
| JP2595574B2 (en) | 1987-11-06 | 1997-04-02 | ミノルタ株式会社 | Photoconductor |
-
1990
- 1990-05-08 WO PCT/NL1990/000066 patent/WO1991017485A1/en not_active Ceased
- 1990-05-08 EP EP95202276A patent/EP0690350B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0690350A2 (en) | 1996-01-03 |
| EP0690350A3 (en) | 1996-07-03 |
| WO1991017485A1 (en) | 1991-11-14 |
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