Field of the Invention
[0001] The present invention relates to a liquid spray-coating method, and to an electrophotographic
photoreceptor formed by the method which can be widely used for electrophotographic
applications such as copiers, laser beam printers, CRT printers and photoengraving
systems.
Discussion of the Background
[0002] Conventionally, inorganic photoconductive materials such as selenium and zinc oxide
have been used for photosensitive layers of electrophotographic photoreceptors.
[0003] Recently, organic photoconductive materials for use in the photosensitive layers
have been investigated, and further a functionally separated photoreceptor including
two layers was mainly investigated. One layer is a charge generation layer absorbing
light and generating a charge carrier, and the other is a charge transport layer transporting
the charge carrier.
[0004] The functionally separated photoreceptor comprises a combination of an organic compound
efficiently generating charge and an organic compound efficiently transporting the
charge. Thus, the photoreceptor has high sensitivity and is in practical use.
[0005] In addition, due to requirements of digitization, high-quality image and high durability,
many photoreceptors such as a photoreceptor having an undercoat layer between the
electroconductive substrate and the photosensitive layer and a photoreceptor having
a protective layer on the photosensitive layer have been invented.
[0006] Many photoreceptors having high chargeability, preventing moire and image deformation,
and having high durability and environmental resistance have been invented by providing
undercoat layers and protective layers having a thickness of from submicrons to a
few microns and including fine particles, either organic or inorganic, uniformly dispersed
in the layers on the photoreceptors.
[0007] These inventions contribute to the progress of image forming apparatus using various
electrophotographic processes typified by a copier.
[0008] Such layers are typically coated on a cylindrical drum substrate or an endless belt-shaped
substrate, etc. to form organic photoreceptors. As the coating methods, a dip coating
method, a spray coating method, a nozzle coating method, etc. are known.
[0009] Hereinafter, the above-mentioned coating methods will be explained.
Dip coating method
[0010] The dip coating method is industrially used most and has been subject of extensive
research. However, the method has a disadvantage that much coating liquid is consumed
when coating an endless belt-shaped substrate which has a large diameter and a cylindrical
drum substrate which is long in many cases. In addition, a low molecular-weight compound
in a layer previously coated on a substrate tends to be dissolved out when coating
a functionally separated photoreceptor because of dipping the substrate into the coating
liquid and drawing up the substrate therefrom, resulting in quality deterioration
of the resultant photoreceptor. Further, the compound dissolved out in the coating
liquid often contaminates the coating liquid and largely affects the coating method.
[0011] Particularly, when forming a protective layer on a functionally separated photoreceptor
having a charge transport layer on a charge generation layer by the dip coating method,
a serious problem of deterioration of basic charge transportability occurs because
a low molecular-weight charge transport compound in the charge transport layer is
dissolved out in the liquid.
Nozzle coating method
[0012] The nozzle coating method is advantageous for coating an endless belt-shaped substrate
which has a large diameter and a cylindrical drum substrate which is long in many
cases
because the consumption of the coating liquid is small. However, a part of the substrate
doubly coated at the beginning and the end of coating becomes thick, and technical
difficulty to solve the problem is high.
[0013] In addition, the method is not suitable for industrial use because mechanical precision
required for the coating apparatus is unrealistically high.
Spray coating method
[0014] The spray coating method is also advantageous for coating an endless belt-shaped
substrate which has a large diameter and a cylindrical drum substrate which is long
in many cases
because the consumption of the coating liquid is small. Further, the method does not
have the problem of thickening a part of the substrate doubly coated at the beginning
and the end of coating, and is industrially used on occasion.
[0015] In addition, even when coating a conventional cylindrical drum substrate, a low molecular-weight
compound does not tend to dissolve out from a layer previously coated and quality
deterioration of the resultant photoreceptor can be prevented. Particularly, the method
is advantageous for coating a protective layer on a functionally separated photoreceptor
having a charge transport layer on the charge generation layer.
[0016] However, usually a solvent having a slow evaporation speed is used in a conventional
spray coating method in many cases to make the coated surface smooth. Therefore, it
generally takes time to dry the coated substrate to the touch in the coater even after
the spray is stopped. In addition, the spray often stops when a coated subject is
transferred.
[0017] In particular, when the coating liquid is a fine-particle dispersion liquid including
at least a solvent and fine particles, the fine particles tend to sink in the spray
coating apparatus and clog the spray gun when the spraying is stopped, resulting in
deterioration of stable coating and coating irregularity.
[0018] This is a case for general spray coating methods, and Japanese Laid-Open Patent Publication
No. 9-75794 discloses an air spray coating method and an apparatus supplying and transporting
a coating liquid without retaining the liquid in the spray coating apparatus (a spray
gun).
[0019] However, it is typically required in coating an undercoat layer and a protective
layer of an electrophotographic photoreceptor that a thin and uniformly dispersed
layer having a thickness of from about submicrons to a few microns should be formed
for their specific electric properties. Therefore, when an electrophotographic photoreceptor
is formed by spray coating, it is necessary to precisely transport small flow rate
of the liquid to the spray coating apparatus.
[0020] With such a small flow rate, the sedimentation of the fine particles in the spray
coating device and the liquid transport route cannot be sufficiently prevented when
the spraying is stopped in such a coating apparatus as has a circular route in which
the coating liquid simply returns to the liquid tank from the coating device. Therefore,
the spray gun tends to be clogged.
[0021] In addition, Japanese Laid-Open Patent Publication No. 58-174264 discloses a spray
coating apparatus circulating a coating liquid. The apparatus has the following circulation
routes:
(1) a coating liquid tank;
(2) a pump;
(3) a coating-liquid feeding pipe;
(4) a spray gun;
(5) a coating-liquid returning pipe; and
(1) the coating-liquid tank,
wherein a bypass pipe is connected to the route between the pump (2) and the coating-liquid
feeding pipe (3) and to the route between the coating-liquid returning pipe (5) and
the coating-liquid tank (1) to prevent the precipitaion of the liquid, and the reservoir
liquid in the tank is forcibly agitated by the divided coating liquid. However, this
apparatus makes coating with a large flow rate, and when such a flow rate of the liquid
as can sufficiently prevent the sedimentation of the fine particles in the coating
device and the transport route when the spraying is stopped is transported, the transported
liquid is too much to form a thin and uniformly dispersed layer having a thickness
of from about submicrons to a few microns required for an electrophotographic photoreceptor.
[0022] Further, when a small flow rate of the liquid is precisely transported to the spray
coating device by the spray coating method to form an electrophotographic photoreceptor,
the sedimentation of the fine particles tends to occur in the fine-particles dispersion-liquid
supplier as well.
[0023] Particularly, when a syringe pump capable of precisely transporting small flow rate
of the liquid to the spray coating device is used as a fine-particle dispersion-liquid
supplier instead of liquid suppliers liable to bring pulsation such as a diaphragm
pump and a gear pump, the dispersion liquid is retained in the cylinder and the sedimentation
of the fine particles tends to go on because it is effective on production efficiency
to stop the syringe pump as well when the spraying is stopped.
Further, there also is a case where the rheology of the liquid changes.
[0024] In this case, since the liquid capacity (cylinder capacity) of the liquid supplier
is far larger than that of the spray coating device, the adverse effect of the fine-particle
sedimentation in the liquid supplier is more serious than that in the spray coating
device.
[0025] Namely, when a dispersed layer is formed by spraying with the liquid in which the
fine-particle sedimentation went on,
the supernatant liquid including less fine particles is sprayed to form the dispersed
layer. Consequently, the fine-particle content in the solid contents included in the
dispersion liquid differs from that in the formed dispersion layer, which causes a
considerable adverse effect on the electric properties, durability, etc. of the resultant
electrophotographic photoreceptor.
SUMMARY OF THE INVENTION
[0026] Accordingly, an object of the present invention is to provide a coating method and
a coating apparatus capable of forming a coated layer having a uniform composition.
[0027] Another object of the present invention is to provide a coating method and a coating
apparatus capable of forming a coated layer having a uniform composition without a
clogging of the spray coating device when the coating liquid is a liquid dispersing
fine particles. In other words, a method and an apparatus forming a coated layer having
a uniform composition are provided, by a circulation-type spray coating method in
which the liquid constantly flows in the liquid supplier, the spray coating device
and the liquid feeding route when the spraying is stopped to prevent the heterogeneous
liquid composition.
[0028] Yet another object of the present invention is to provide an electrophotographic
photoreceptor having a layer including a uniform composition using the above-mentioned
method and apparatus.
[0029] Briefly these objects and other objects of the present invention as hereinafter will
become more readily apparent can be attained by a method for manufacturing an electrophotographic
photoreceptor using a circulation-type spray coating apparatus including at least
a liquid supplier, a spray coating device atomizing and spraying the liquid, a liquid
feeding route in which the liquid is transported from a liquid tank through the liquid
supplier to the spray coating device, a liquid circulating route in which the liquid
returns to the liquid tank from the spray coating device and a liquid pressurizer,
wherein the liquid constantly flows in the liquid supplier, the spray coating device
and the liquid feeding route.
[0030] These and other objects, features and advantages of the present invention will become
apparent upon consideration of the following description of the preferred embodiments
of the present invention taken in conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0031] Various other objects, features and attendant advantages of the present invention
will be more fully appreciated as the same becomes better understood from the detailed
description when considered in connection with the accompanying drawings in which
like reference characters designate like corresponding parts throughout and wherein:
Fig. 1 is a schematic view illustrating an outline of the method for manufacturing
an electrophotographic photoreceptor in the present invention;
Fig. 2 is a schematic view illustrating an embodiment of the liquid supplier of the
present invention;
Fig. 3. is a schematic view:illustrating another embodiment of the liquid supplier
of the present invention;
Fig. 4 is a schematic view illustrating yet other three embodiments of the liquid
supplier of the present invention;
Fig. 5 is a schematic view illustrating an embodiment of the spray coating device
of the present invention;
Fig. 6 is a schematic view illustrating a cross section of the photosensitive layer
of a functionally separated electrophotographic photoreceptor having an undercoat
layer.
Fig. 7 is a schematic view illustrating a cross section of the photosensitive layer
of a functionally separated electrophotographic photoreceptor having a protective
layer; and
Fig. 8 is a schematic view illustrating a cross section of the photosensitive layer
of a functionally separated electrophotographic photoreceptor having an undercoat
layer and a protective layer.
DETAILED DESCRIPTION OF THE INVENTION
[0032] Generally, the present invention provides a manufacturing method and an apparatus
preferably used for coating such a liquid as loses its homogeneity due to the retention,
particularly the method and the apparatus are preferably used for spray coating of
a fine-particle dispersion liquid. The method and the apparatus of the present invention
prevent the spray gun from clogging, and equalize the content ratio of the fine particles
of the solid content included in the dispersion liquid and that of the formed dispersed
layer.
In addition, the method and the apparatus can form a thin and uniform coated layer
having a thickness of from about sub
µm to some µm.
[0033] The manufacturing method and the apparatus of the present invention are particularly
suitable for forming a photosensitive layer of an electrophotographic photoreceptor.
However, the present invention is not limited hereto, and applicable for the fields
besides the electrophotographies.
[0034] Therefore, hereinafter, a case where a fine-particle dispersion liquid is used as
a coating liquid will be explained, however, the present invention is not limited
to this case. Besides the fine-particle dispersion liquid, dye-solution liquids, resin-solution
liquids, emulsion liquids and the like liquids can be used as the coating liquids.
[0035] A syringe pump can be preferably used as the liquid supplier for use in the present
invention. The syringe pump includes at least a cylinder, a piston rod having a piston
member capable of being freely inserted into the cylinder and a means of driving the
piston rod, and precisely supplies a small flow rate of the liquid to the above-mentioned
spray coating device by driving the piston rod when the spraying is performed. The
syringe pump preferably has a liquid-flow duct in the cylinder or in the piston rod.
Particularly, the piston rod preferably includes the liquid-flow duct, for example,
it is preferable to use a syringe pump having a piston rod including at least an entrance
and an exit for the liquid circulation, and the liquid-flow duct, in which the fine-particle
dispersion liquid can constantly flow without staying in the cylinder when the spraying
is stopped.
[0036] The spray coating device for use in the present invention is an air spray gun including
at least a coating nozzle and an air cap, in which the pressure-fed liquid to the
coating nozzle is atomized by compressed air discharge from the air cap. In addition,
the coating nozzle has at least a liquid-feed opening and an exit opening for the
liquid circulation besides a discharge opening for the atomized liquid, and the liquid
can constantly flow without staying in the spray gun when the spraying is stopped.
[0037] In the liquid feeding and circulating route of the present invention including a
liquid feeding route in which the liquid is transported to the spray coating device
through the liquid supplier from a liquid tank; a circulating route in which the liquid
returns to the liquid tank from the spray coating device; and a pressurizer for circulating
the liquid, the liquid feeding route between the liquid tank and the liquid supplier
and the circulating route between the spray coating device and the liquid tank respectively
have one liquid-pressure blocker or more which blocks the liquid pressure given by
the pressurizer. When the circulation is stopped by blocking the liquid pressure when
the spraying is performed, the liquid pressure between the liquid supplier and the
spray coating device is separated from the liquid pressure given by the pressurizer
and equals the pressure given by the liquid supplier. Thus, the liquid feeding and
circulating route of the present invention can spray by the pressure of the liquid
supplier.
[0038] In the present invention, "the liquid supplier" mainly gives the discharging pressure
of the spray coating device, and "the pressurizer for circulation" mainly controls
the liquid circulation of the whole coating apparatus. In addition, the liquid supplier
is preferably located between the pressurizer for circulation and the spray coating
device.
[0039] When the flow rate of the dispersion liquid by the liquid pressure of the pressurizer
for the liquid circulation is Fa (cc/min.) and that of the fine-particle dispersion
liquid supplier is Fb (cc/min.), the following relationship is preferably satisfied:

[0040] When manufacturing an electrophotographic photoreceptor, the Fa is preferably from
300 to 1,500 cc/min, and the Fb is preferably from 5 to 100 cc/min.
[0041] The details of the present invention will be explained, referring to the drawings.
However, the drawing is an example, and the present invention is not limited to the
embodiments.
[0042] First, the operation when the spraying is stopped will be explained.
[0043] Fig. 1 is a schematic view illustrating an outline of the method for manufacturing
an electrophotographic photoreceptor in the present invention.
[0044] A fine-particle dispersion liquid 2 put and agitated in a coating liquid tank 1 is
transported by the pressure of a pressurizer for circulation 3 to a liquid supplier
6 and a spray coating device 7 through a liquid feeding route 4, and then returned
to the coating liquid tank 1 through a circulation route 8. At this point, liquid-pressure
blockers 5 located in the liquid feeding route 4 and the circulation route 8 are disengaged.
As the pressurizer for circulation, gear pumps, diaphragm pumps and the like pumps
are preferably used, which can give sufficient flow rate to prevent the sedimentation
of the fine particles.
[0045] Particularly, the details of the liquid supplier 6 when the spraying is stopped will
be explained, referring to Fig. 2.
[0046] Fig. 2 is a schematic view illustrating an embodiment of the liquid supplier of the
present invention. The liquid supplier is a syringe pump including a cylinder 11;
a piston member 17; and a piston rod 12, and the piston rod 12 includes a circulation-liquid
entrance 14, a circulation-liquid exit 15 and a circulation-liquid flow duct 16.
[0047] The fine-particle dispersion liquid 2 pressurized by the pressurizer for circulation
3 in Fig. 1 enters the circulation-liquid entrance 14 of the piston rod 12 connected
to the liquid feeding route 4 and is supplied inside the cylinder 11 from the circulation-liquid
exit 15 through the circulation-liquid flow duct 16 penetrating the piston rod 12.
[0048] Then, after filling the inside of the cylinder 11, the fine-particle dispersion liquid
2 is transported to the spray coating device 7 through the liquid feeding route 4
connected to the upper part of the cylinder. When the spraying is stopped, the liquid
supplier 6 stops as well and the piston rod 12 stays waiting in the bottom dead center.
[0049] The capacity of the cylinder 11 is preferably larger than the quantity of the dispersion
liquid required for spray coating at a time. However, the capacity which is larger
than necessary is not preferable because of being a cause of deteriorating the preciseness
of the liquid feeding when the spraying is performed.
[0050] Because of being the above-mentioned structure, the fine-particle dispersion liquid
2 can flow without staying in the cylinder 11 when the spraying is stopped. Therefore,
the pressurizer for circulation 3 can give a liquid pressure such that sufficient
circulating flow-rate can be obtained, regardless of the strength of the liquid pressure
for spray coating. In addition, the sedimentation of the fine particles in the spray
coating device 7 and the cylinder 11 can be prevented.
[0051] The circulating direction of the fine-particle dispersion liquid 2 is not limited
thereto.
[0052] Namely, the liquid feeding route 4 from the pressurizer for circulation 3 may be
connected to the upper part of the
cylinder, and the fine-particle dispersion liquid 2 may be supplied inside the cylinder
11 through the route and transported to the spray coating device 7 through the circulation-liquid
flow duct 16 penetrating the piston rod 12 after filling the inside of the cylinder
11. In this case, the numeral 15 is a circulation-liquid entrance, and the numeral
14 is an exit.
[0053] Fig 3. and Fig. 4 are schematic views illustrating other embodiments of the liquid
supplier of the present invention.
[0054] Fig. 3 is an example in which circulation-liquid flow ducts are formed inside a piston
rod 12 and a piston member 17, which enable the liquid to flow uniformly inside the
cylinder when the spraying is stopped. Fig. 4 shows three examples in which circulation-liquid
entrances 14 are formed on the wall of cylinders 11. A in Fig. 4 is an example in
which the liquid entrances is formed in the top dead center, B in Fig. 4 is an example
in which the entrance is formed in the bottom dead center and C in Fig. 4 shows an
example in which plural entrances are formed. The plural entrances are preferable
for uniformity of the liquid flow inside the cylinder when the spraying is stopped.
[0055] The details of the spray coating device 7 will be explained when the spraying is
stopped, referring to Fig. 5.
[0056] Fig. 5 is a schematic view illustrating an embodiment of the spray coating device
of the present invention.
[0057] The fine-particle dispersion liquid 2 is supplied to the coating nozzle 21 through
the liquid feeding route 4 connected to a liquid-feed opening 24. Then the dispersion
liquid 2 fills the inside of the coating nozzle 21, and returns to the coating liquid
tank 1 through the circulation route 8 connected to a circulation exit 25.
[0058] When the spraying is stopped, an atomized-liquid discharger 23 is closed by a needle
valve 26. The coating nozzle 21 may be a single piece with a spray gun 27, or may
be detachably equipped with the spray gun 27 by a threaded type method.
[0059] In addition, the needle valve 26 is preferably structured such that the liquid leak
is prevented by a gasket (not shown) at the rear end of the coating nozzle (the opposite
side of the atomized-liquid discharger 23).
[0060] Next, the operation when the spraying is performed will be explained.
[0061] When the pressurizer for circulation 3 is stopped and the liquid circulation is blocked
by the one or more liquid-pressure blockers 5 such as valves located on the liquid
feeding route 4 and the circulation route 8 respectively, the liquid supplier 6 and
the spray coating device 7 become independent of the circulating system.
[0062] At this point, the preferable operation order of the one or more liquid-pressure
blockers 5 such as valves located on the liquid feeding route 4 and the circulation
route 8 respectively is as follows:
the liquid-pressure blockers 5 such as valves located on the liquid feeding route
4 in the upstream of the circulation are activated first to block the liquid pressure;
and
the liquid-pressure blockers 5 such as valves located on the circulation route 8 in
the downstream of the circulation are activated.
[0063] Thus, the residual pressure given by the pressurizer for circulation 3 retained between
the one or more liquid-pressure blockers 5 located on the liquid feeding route 4 and
the circulation route 8 respectively is released.
[0064] The liquid-pressure blockers 5 on the liquid feeding route 4 are preferably located
between the pressurizer for circulation 3 and the liquid supplier 6 in view of the
liquid-pressure stability.
[0065] In succession, in the liquid supplier 6 in Fig. 2, the piston rod 12 which stayed
waiting in the bottom dead center begins to go up by the driving force of a stepping
motor 13b through a ball screw 13a. In the cylinder 11, the liquid pressure having
very little fluctuation is given to the dispersion liquid 2 filled and supplied in
the cylinder when the liquid is circulated. Thus, the small flow rate of the dispersion
liquid 2 can be precisely transported to the spray coating device 7 by fixing the
lifting speed of the piston rod 12.
[0066] Because of these consecutive operations, the liquid pressure between the liquid-pressure
blockers 5 located on the liquid feeding route 4 and the circulation route 8, i.e.,
the liquid pressure in and between the liquid supplier 6 and the spray coating device
7 equals the liquid pressure given by the liquid supplier.
[0067] Further, in the spray coating device 7 in Fig. 5, the needle valve 26 which closed
the atomized liquid discharger 23 opens, and a small quantity of the liquid having
very little fluctuation can be discharged from the atomized liquid discharger 23 by
the liquid pressure for spray coating given by the liquid supplier 6 to the dispersion
liquid 2, regardless of the circulating liquid flow-rate.
[0068] The discharged dispersion liquid 2 is sprayed by the air for atomization supplied
to an air cap 22 through another route (not shown). Thus, a thin and uniform dispersed
layer having a thickness of from about submicrons to a few microns can be formed by
spray coating.
[0069] When the spraying is stopped, the liquid-pressure blockers located on the liquid
feeding route 4 and the circulation route 8 are released again, and the pressurizer
for circulation 3 begins the circulation. At this point, in the liquid supplier in
Fig. 2, the piston rod 12 returns to the bottom dead center and stays waiting.
[0070] As for the relationship between the circulating flow rate when the spraying is stopped
and the liquid feeding flow rate when the spraying is performed, when the circulation
flow rate when the spraying is stopped is Fa and the liquid feeding flow rate when
the spraying is performed is Fb, Fa has to be sufficiently large such that the sedimentation
of the fine particles in the liquid supplier 6 and the spray coating device 7 may
not be formed, and Fb has to be sufficiently small such that a thin and uniform dispersed
layer having a thickness of from about submicrons to a few microns can be formed.
In the method for manufacturing an electrophotographic photoreceptor, functional separation
to make Fa and Fb different from each other is important such that the following relationship
can be satisfied:

[0071] The present invention is an embodiment of the method for manufacturing an electrophotographic
photoreceptor.
[0072] In addition, in a continuous long-time manufacturing process, the following relationship
between Fa and Fb is particularly preferable:

[0073] Next, cases where the electrophotographic photoreceptors of the present invention
are manufactured will be explained, referring to Figs. 6 to 8.
[0074] Fig. 6 is a schematic view illustrating a cross section of a functionally separated
electrophotographic photoreceptor, in which an undercoat layer 32, a charge generation
layer (CGL) 33, a charge transport layer (CTL) 34 are layered in this order on an
electroconductive substrate 31.
[0075] Fig. 7 is a schematic view illustrating a cross section of a functionally separated
electrophotographic photoreceptor, in which a charge generation layer (CGL) 33, a
charge transport layer (CTL) 34 and a protective layer 35 are layered in this order
on an electroconductive substrate 31.
[0076] Fig. 8 is a schematic view illustrating a cross section of a functionally separated
electrophotographic photoreceptor, in which an undercoat layer 32, a charge generation
layer (CGL) 33, a charge transport layer (CTL) 34 and a protective layer 35 are layered
in this order on an electroconductive substrate 31.
[0077] The layered order of the charge generation layer (CGL) 33 and the charge transport
layer (CTL) 34 may be reversible. Further, these layers may be a single layer including
a charge generation material and a charge transport material.
[0078] As the electroconductive substrate, various known substrates can be used. For example,
a metallic drum made of aluminium, copper, nickel, stainless, steel and the like,
and substrates such as plastic films, plastic drums, glass drums and papers whose
surfaces are applied with an electroconductive treatment can be used. Specific examples
of the substrates applied with an electroconductive treatment include such as substrates
laminated with a metallic foil; substrates evaporated or sputtered with a metal, an
electroconductive oxide and the like; and substrates coated with electroconductive
materials such as metallic powders, carbon black, copper iodide and tin oxide, which
are optionally coated together with a binder resin. Among these substrates, metallic
drums, plastic films applied with an electroconductive treatment and plastic drums
can be preferably used.
[0079] The undercoat layer 32 typically includes a resin as a main component. Considering
that the photosensitive layer is coated on the undercoat layer using a solvent, the
resin preferably has good solvent resistance against the organic solvent used for
coating the photosensitive layer.
[0080] Specific examples of such resins include watersoluble resins such as polyvinylalcohol,
casein, polyacrylic natrium; alcohol-soluble resins such as nylon copolymer and nylon
methoxymethylate; and cured resins forming three-dimensional network structures such
as polyurethane, melamine resins, alkyd-melamine resins and epoxy resins.
[0081] In addition, fine particles of a metal oxide such as titanium oxide, silica, alumina,
zirconium oxide, tin oxide and indium oxide or of a metal sulfide and metal nitride,
or of these fine particles applied with electroconductive treatments may be optionally
included in the undercoat layer. Or, organic fine particles such as fluorocarbon resins,
silicone resins, acryl resins, melamine resins can be used.
[0082] The undercoat layer 32 can be formed by a dip coating method, a spray coating method,
a bead coating method, etc. The thus formed undercoat layer 32 preferably has a thickness
of form about 0.1 to 15 µm, and more preferably from 0.3 to 5 µm.
[0083] In case of spray coating, the manufacturing method of the present invention can be
used to form the undercoat layer 32.
[0084] Namely, the fine-particle dispersion liquid 2 including at least a solvent and fine
particles for use in the present invention is formed by selecting from the above-mentioned
fine particles for the undercoat layer 32 and the group of resin materials, and properly
dispersing the materials with a ball mill, an attritor and a sand mill, etc.
[0085] Next, the charge generation layer 33 will be explained.
[0086] The charge generation layer 33 includes a charge generation material as a main component,
and a binder resin can be optionally used in the charge generation layer. As the charge
generation material, inorganic materials or organic materials can be used.
[0087] Specific examples of the inorganic materials include crystallized selenium, amorphous
selenium, selenium-tellurium, selenium-tellurium-halogen, selenium-arsenic compound,
amorphous silicon, etc. As for the amorphous silicon, amorphous silicon formed from
a dangling bond terminated with a hydrogen atom or a halogen atom, and amorphous silicon
formed from a doped boron atom, a phosphorous atom, etc. are preferably used.
[0088] On the other hand, as the organic material, known materials can be used. For examples,
phthalocyanine pigments such as metal phthalocyanine and metal-free phthalocyanine,
azulenium salt pigments, squaric acid methine pigments, azo pigments having carbazole
skeletons, azo pigments having triphenylamine skeletons, azo pigments having diphenylamine
skeletons, azo pigments having dibenzothiophene skeletons, azo pigments having fluorenone
skeletons, azo pigments having oxadiazole skeletons, azo pigments having bisstilbene
skeletons, azo pigments having distyryloxadiazole skeletons, azo pigments having distyrylcarbazole
skeletons, perylene pigments, anthraquinone or polycyclic quinone pigments, quinoneimine
pigments, diphenylmethane and triphenylmethane pigments, benzoquinone and naphthoquinone
pigments, cyanine and azomethine pigments, indigoid pigments, bisbenzimidazole pigments
and the like pigments can be used.
[0089] These charge generation materials may be used alone or in combination.
[0090] Specific examples of the binder resins optionally used for the charge generation
layer 33 include polyamide, polyurethane, epoxy resins, polyketone, polycarbonate,
silicone resins, acryl resins, polyvinylbutyral, polyvinylformal, polyvinylketone,
polystyrene, poly-N-vinylcarbazole, polyacrylamide and the like resins. These binder
resins can be used alone or in combination.
[0091] In addition, a charge transport material may be optionally included in the charge
generation layer. Besides the above-mentioned binder resins, a high-molecular weight
charge transport material may be used as the binder resin for the charge generation
layer 33.
[0092] As a method for forming the charge generation layer 33, a vacuum thin-film manufacturing
method, a casting method from liquid-solution dispersion methods, etc. can be used.
[0093] Specific examples of the vacuum thin-film manufacturing method include a vacuum-deposition
method, a glow-discharge polymerization method, an ion-plating method, a sputtering
method, a reactive sputtering method, CVD method, etc.
[0094] In order to form the charge generation layer 33 by the casting method, the above-mentioned
materials are optionally dispersed with a binder resin by a ball mill, an attritor,
a sand mill, etc. using a solvent such as tetrahydrofuran, cyclohexane, dioxane and
butanone; and the dispersion liquid properly diluted is coated to form the charge
generation layer.
[0095] A dip coating method, a spray coating method, a bead coating method, etc. can be
used for coating the charge generation layer.
[0096] The thus formed charge generation layer 33 preferably has a thickness of from about
0.01 to 5 µm, and more preferably from 0.05 to 2 µm.
[0097] In case of using the spray coating method, the manufacturing method of the present
invention can be used for forming the charge generation layer 33.
[0098] Namely, the fine-particle dispersion liquid 2 including at least a solvent and fine
particles for use in the present invention is formed by selecting from the above-mentioned
fine particles of the charge generation materials and the group of resin materials
as the components, and properly dispersing the materials with a ball mill, an attritor
and a sand mill, etc.
[0099] Next, the charge transport layer 34 will be explained.
[0100] The charge transport layer 34 includes a charge transport material and a binder resin.
The charge transport material and the binder resin are properly dissolved or dispersed
in a solvent, and this is coated and dried to form the charge transport layer. Optionally,
a plasticizer, an antioxidant, a leveling agent, etc. may be included in the charge
transport layer besides the charge transport material and the binder resin.
[0101] As the charge transport material, positive-hole transport materials and electron
transport materials are available.
[0102] As the electron transport materials, known materials can be used. Specific examples
of the electron transport materials include electron acceptors such as chloranil,
bromanil, tetracyanoethylene, tetracyanoquinodimethane, 2,4,7-trinitro-9-fluorenon,2,4,5,7-7-tetranitro-9-fluorenon,
2,4,5,7-tetranitroxanthone, 2,4,8-trinitrothioxanthone, 2,6,8-trinitro-4H-indeno [1,2-b]
thiophene-4-one and 1,3,7-trinitrodibenzothiophene-5,5-dioxides.
[0103] These electron transport materials can be used alone in combination.
[0104] As the positive-hole transport material, the following known electron-releasing materials
can be used. For example, oxazole derivatives, oxadiazole derivatives, imidazole derivatives,
triphenylamine derivatives, 9-(p-diethylaminostyrylanthracene),1,1-bis-(4-dibenzilaminophenyl)propane,
styrylanthracene, styrylpyrazoline, phenylhydrazone, α-phenylstilbene derivatives,
thiazole derivatives, triazole derivatives, phenazine derivatives, acridine derivatives,
benzofuran derivatives, benzimidazole derivatives and thiophene derivatives, etc.
can be used. These positive-hole transport materials can be used alone in combination.
[0105] In addition, as a high-molecular-weight charge transport material, the following
materials are available when classified by their structures.
(a) Polymers having carbazole rings
[0106] For example, poly-N-vinylcarbazole, and the compounds disclosed in Japanese Laid-Open
Patent Publications Nos. 50-82056, 54-9632, 54-11737,4-175337,4-183719 and 6-234841
are available.
(b) Polymers having hydrazone structures
[0107] For example, the compounds disclosed in Japanese Laid-Open Publications Nos. 57-78402,
61-20953, 61-296358, 1-134456, 1-179164, 3-180851, 3-180852, 3-50555, 5-310904 and
6-234840 are available.
(c) Polysilylene polymers
[0108] For example, the compounds disclosed in Japanese Laid-Open Publications Nos. 63-285552,
1-88461, 4-264130, 4-264131,4-264132, 4-264133 and 4-289867 are available.
(d) Polymers having triarylamine structures
[0109] For example, N,N-bis(4-methylphenyl)-4-aminopolystyrene, and the compounds disclosed
in Japanese Laid-Open Publications Nos. 1-134457, 2-282264, 2-304456, 4-133065, 4-133066,
5-40350 and 5-202135 are available.
(e) Other polymers
[0110] For example, formaldehyde condensation polymer of nitropyrene, and the compounds
disclosed in Japanese Laid-Open Publications Nos. 51-73888, 56-150749, 6-234836 and
6-234837 are available.
[0111] Specific examples of the binder resins for use in the charge transport layer 34 include
vinyl polymers such as polyvinylbutyral, polyvinylacetal, polyester, polycarbonate,
polystyrene, polyestercarbonate, polysulfone, polyimide, polymethylmethacrylate and
poly vinyl chloride, and their copolymers; and resins such as phenoxy resins, epoxy
resins and silicone resins, or partially crosslinked resins thereof. These resins
can be used alone or in combination.
[0112] The charge transport layer preferably has a thickness of from about 5 to 100 µm,
and more preferably from 10 to 30 µm. An antioxidant and a plasticizer used for a
rubber, a plastic, a fat, etc. can be included in the charge transport layer 34.
[0113] A leveling agent can be included in the charge transport layer 34. As the leveling
agent, silicone oils such as a dimethyl silicone oil and a methyl phenyl silicone
oil; and a polymer or an oligomer having a perfluoroalkyl group can be used. The content
of the leveling agent is preferably from'0 to 1 part by weight per 100 parts by weight
of the binder resin.
[0114] Fine particles can be included in the charge transport layer 34. Specific examples
of the fine particles include inorganic fine particles such as titanium oxide, silica,
tin oxide, aluminum oxide, zirconium oxide, indium oxide, silicon nitride, calcium
oxide, zinc oxide and barium sulfate; or organic fine particles such as fluorocarbon
resins, silicone resins, acryl resins and melamine resins.
[0115] A dip coating method, a spray coating method, a bead coating method, etc. can be
used for coating the charge transport layer.
[0116] When a dispersion liquid including fine particles is coated by the spray coating
method, the manufacturing method of the present invention can be used for forming
the charge transport layer 34.
[0117] Namely, the fine-particle dispersion liquid 2 including at least a solvent and fine
particles for use in the present invention is formed by selecting from the above-mentioned
fine particles of the charge transport materials and the group of resin materials
as the components, and properly dispersing the materials with a ball mill, an attritor
and a sand mill, etc.
[0118] Next, the protective layer 35 will be explained.
[0119] The protective layer includes fine particles and a binder resin, and a charge transport
material can be optionally included in the protective layer.
[0120] Specific examples of the fine particles include inorganic fine particles such as
titanium oxide, silica, tin oxide, aluminum oxide, zirconium oxide, indium oxide,
silicon nitride, calcium oxide, zinc oxide and barium sulfate; or organic fine particles
such as fluorocarbon resins, silicone resins, acryl resins and melamine resins.
[0121] The surface of these fine particles may be treated with an inorganic or an organic
substance for the purpose of increasing the dispersibility. Specific examples of the
surface treatment include a water-repellent treatment such as a silane-coupling agent
treatment, a fluorochemical silane-coupling agent treatment and a higher fatty-acid
treatment. As the inorganic substance treatment, a filler whose surface is treated
with alumina, zirconia, tin oxide and silica can be used.
[0122] Specific examples of the binder resins include vinyl polymers such as polyvinylbutyral,
polyvinylacetal, polyester, polycarbonate, polystyrene, polyestercarbonate, polysulfone,
polyimide, polymethylmethacrylate and poly vinyl chloride, and their copolymers; and
resins such as phenoxy resins, epoxy resins and silicone resins, or partially crosslinked
resins thereof. These resins can be used alone or in combination.
[0123] The same charge transport material which can be included in the charge transport
layer 34 can be optionally included in the protective layer.
[0124] The protective layer 35 can be formed by a dip coating method, a spray coating method,
a bead coating method, etc. The thus formed protective layer 35 preferably has a thickness
of from about 0.1 to 20 µm, and more preferably from 0.5 to 10 µm.
[0125] In case of using the spray coating, the manufacturing method of the present invention
can be used for forming the protective layer 35.
[0126] Namely, the fine-particle dispersion liquid 2 including at least a solvent and fine
particles for use in the present invention is formed by selecting from the above-mentioned
fine particles for the protective layer 35 and the group of resin materials as the
components, and properly dispersing the materials with a ball mill, an attritor and
a sand mill, etc.
[0127] Various solvents may be used for the coating liquids forming the above-mentioned
each layer 32 to 35 of an electrophotographic photoreceptor. Specific examples of
the solvent include ethers such as diethylether, dimethoxymethane, tetrahydrofuran
and 1,2-dimethoxyethane; carbon hydrides such as toluene and xylene; ketones such
as acetone, methyl ethyl ketone and cyclohexanone; esters such as methyl acetate and
ethyl acetate; and alcohols such as methanol, ethanol and propanol. These solvents
can be used alone or in combination.
[0128] Having generally described this invention, further understanding can be obtained
by reference to certain specific examples which are provided herein for the purpose
of illustration only and are not intended to be limiting. In the descriptions in the
following examples, the numbers represent weight ratios in parts, unless otherwise
specified.
EXAMPLES
[0129] The following dispersion liquids having the respective components were prepared to
form an electrophotographic photoreceptor.
Dispersion liquid A for coating an undercoat layer
[0130] The following materials were dispersed with a ball mill for 100 hrs. to prepare a
dispersion liquid A.
Alkyd resin
(tradename Bekkosol 1307-60-EL from Dainippon Ink & Chemicals, Inc.) |
5 |
Melamine resin
(tradename Super Bekkamin G-821-60 from Dainippon Ink & Chemicals, Inc.) |
5 |
Titanium oxide
(tradename CREL from Ishihara Sangyo Kaisha Ltd.) |
10 |
| Methyl ethyl ketone |
50 |
| Cyclohexanone |
30 |
Dispersion liquid B for coating a charge generation layer
[0131] The following materials were dispersed with a ball mill for 72 hrs. to prepare a
dispersion liquid B.
| Oxotitaniumphthalocyanine pigment |
2 |
Polyvinylbutyral
(tradename XYHL from UCC) |
0.2 |
| Tetrahydrofuran |
132 |
| Cyclohexanone |
88 |
Dispersion liquid C1 for coating a charge transport layer
[0132] The following materials were dispersed with a ball mill for 72 hrs. to prepare a
dispersion liquid C1.

Liquid solution C2 for coating a charge transport layer
[0133] The following materials were dissolved to prepare a liquid solution C2.
Tetrahydrofuran liquid solution including 200 parts of tetrahydrofuran, 135 parts
of cyclohexanone and 1 % of silicone oil
(tradename KF50 from Shin-Etsu Silicone Co., Ltd.) |
1 |
| Charge transport material having the Formula (I) |
6 |
Polycarbonate resin
(tradename Z polyca from Teijin Chemicals Ltd. having a viscosity-average molecular
weight of 50,000) |
10 |
Dispersion liquid D for coating a protective layer
[0134] The following materials were dispersed with a ball mill for 24 hrs. to prepare a
dispersion liquid D.
Titanium oxide
(tradename CREL from Ishihara Sangyo Kaisha Ltd.) |
2 |
Polycarbonate resin
(tradename Z polyca from Teijin Chemicals Ltd. having a viscosity-average molecular
weight of 50,000) |
6 |
| Tetrahydrofuran |
190 |
| Cyclohexanone |
70 |
Example 1
[0135] By the circulation-type spray coating method of the present invention shown in Fig.
1, the dispersion liquid A was coated by spraying on a rotating aluminium cylinder
having a diameter of 30 mm to form an undercoat layer 32. When the spraying is performed,
the spray coating device 7 was located 100 mm apart from the rotating aluminium cylinder
and sprayed the cylinder reciprocating in the axial direction of the cylinder at a
predetermined speed. The flow rate of the liquid from the dispersion liquid supplier
6 to the spray coating device 7 was 10 cc/min. when the spraying is performed.
[0136] After the spray was stopped, the cylinder was dried to the touch while rotating for
about 20 min. Then, the rotation was stopped, and the cylinder was taken out to be
dried in a drier. The thickness of the undercoat layer 32 was 5 µm after dried.
[0137] While the cylinder was dried to the touch, and was taken off and put on after the
spray was stopped, the dispersion liquid was circulated by the method of the present
invention. The flow rate of the liquid circulated by the pressurizer for liquid circulation
3 was 800 cc/min.
[0138] Next, another aluminium cylinder having a diameter of 30 mm was set to be sprayed,
which was 30 min. after the spray for the first cylinder was stopped.
[0139] These operations were repeated 10 times to prepare 10 sample rolls.
[0140] Then, spray and stop were repeated 10 times respectively for forming a charge generation
layer 33 with the dispersion liquid B, forming a charge transport layer with the liquid
solution C2 and forming a protective layer 35 with the dispersion liquid D in this
order to prepare 10 photoreceptors. The tenth prepared photoreceptor was a photoreceptor
sample of Example 1.
[0141] The flow rate of the liquid from the dispersion liquid supplier 6 to the spray coating
device 7 was 4 cc/min. when forming the charge generation layer 33 with the dispersion
liquid B, 42 cc/min. when forming the charge transport layer 34 with the liquid solution
C2 and 15 cc/min. when forming the protective layer 35. The thickness of the charge
generation layer 33 was 0.1 µm, that of the charge transport layer was 20 µm and that
of the protective layer was 3 µm after dried.
[0142] When changing each liquid, the cylinder 11 in the dispersion liquid supplier 6 and
the coating nozzle 21 in the spray coating device 7 were disassembled to find no deposition
formed by sedimentation of the dispersed fine particles. In addition, no clogging
was found at the tip of the coating nozzle 21.
[0143] In addition, each liquid discharged from the spray coating device 7 was collected
in a bottle when starting to spray the tenth photoreceptor. Each collected liquid
was a liquid sample of Example 1.
[0144] The concentration of the fine particles in each liquid was determined as follows:
(1) the weight of each liquid was measured;
(2) dissolved components such as resins were sufficiently removed with tetrahydrofuran;
(3) fine particles were separated with a suction filter;
(4) solvent components were dried; and then
(5) the weight of the fine particles was measured.
[0145] As a reference, the concentration of the fine particles in each dispersion liquid
after the liquid was prepared was measured by the same method mentioned above. The
results are shown in Table 1. The fine-particle concentrations of the liquid samples
of Example 1 scarcely changes compared with those of the references. This is appraisable
as an alternative property proving that the reproducibility of the content ratio of
the fine particles in the formed layers is good, compared with that of the fine particles
in the solid contents included in the dispersion liquids.
Comparative Example 1
[0146] The procedure for preparation of 10 photoreceptors in Example 1 was repeated except
that the liquid circulation was stopped with the liquid-pressure blockers 5 to retain
the dispersion liquid in the liquid supplier 6 and the spray coating device 7 when
the spray was stopped. The tenth prepared photoreceptor was a photoreceptor sample
of Comparative Example 1.
[0147] When the cylinder 11 in the dispersion liquid supplier 6 and the coating nozzle 21
in the spray coating device 7 were disassembled in changing each liquid, a deposition
formed by sedimentation of the dispersed fine particles was observed. In addition,
a clogging was found at the tip of the coating nozzle 21.
[0148] In addition, each liquid discharged from the spray coating device 7 was collected
in a bottle when starting to spray the tenth photoreceptor. Each collected liquid
was a liquid sample of Comparative Example 1. The procedure for determination of the
fine-particle concentration of the liquids in Example 1 was repeated to determine
that of the liquids of Comparative Example 1. The results are shown in Table 1. Compared
with those of the liquid samples in Example 1, the fine-particle concentrations of
the liquids decrease. This is appraisable as an alternative property proving that
the reproducibility of the content ratio of the fine particles in the formed layers
is poor, compared with that of the fine particles in the solid contents included in
the dispersion liquids.
Table 1
| Fine-Particle Concentration (wt. %) |
| |
Liquid samples when prepared |
Liquid samples in Example 1 |
Liquid samples in Comparative Example 1 |
| Dispersion liquid A |
9.98 % |
9.97 % |
6.52 % |
| Dispersion liquid B |
0.91 % |
0.90 % |
0.62 % |
| Dispersion liquid D |
0.75 % |
0.74 % |
0.15 % |
Example 2
[0149] The procedure for preparation of 10 photoreceptors in Example 1 was repeated except
for using the dispersion liquid C1 instead of the dispersion liquid C2. The tenth
prepared photoreceptor was a photoreceptor sample of Example 2.
[0150] When changing each liquid, the cylinder 11 in the dispersion liquid supplier 6 and
the coating nozzle 21 in the spray coating device 7 were disassembled to find no deposition
formed by sedimentation of the dispersed fine particles.
In addition, no clogging was found at the tip of the coating nozzle 21. In addition,
each liquid discharged from the spray coating device 7 was collected in a bottle when
starting to spray the tenth photoreceptor. Each collected liquid was a liquid sample
of Example 2. The procedure for determination of the fine-particle concentration of
the liquids in Example 1 was repeated to determine that of the liquids of Example
2. The results are shown in Table 2. The fine-particle concentrations of the liquid
samples of Example 2 scarcely changes compared with those of the references. This
is appraisable as an alternative property proving that the reproducibility of the
content ratio of the fine particles in the formed layers is good, compared with that
of the fine particles in the solid contents included in the dispersion liquids.
Comparative Example 2
[0151] The procedure for preparation of 10 photoreceptors in Example 2 was repeated except
that the liquid circulation was stopped with the liquid-pressure blockers 5 to retain
the dispersion liquid in the liquid supplier 6 and the spray coating device 7 when
the spray was stopped. The tenth prepared photoreceptor was a photoreceptor sample
of Comparative Example 2.
[0152] When the cylinder 11 in the dispersion liquid supplier 6 and the coating nozzle 21
in the spray coating device 7 were disassembled in changing each liquid, a deposition
formed by sedimentation of the dispersed fine particles was observed. In addition,
a clogging was found at the tip of the coating nozzle 21.
[0153] In addition, each liquid discharged from the spray coating device 7 was collected
in a bottle when starting to spray the tenth photoreceptor. Each collected liquid
was a liquid sample of Comparative Example 2. The procedure for determination of the
fine-particle concentration of the liquids in Example 1 was repeated to determine
that of the liquids of Comparative Example 2. The results are shown in Table 2. Compared
with those of the liquid samples in Example 2, the fine-particle concentrations of
the liquids decrease. This is appraisable as an alternative property proving that
the reproducibility of the content ratio of the fine particles in the formed layers
is poor, compared with that of the fine particles in the solid contents included in
the dispersion liquids.
Table 2
| Fine-Particle Concentration (wt. %) |
| |
Liquid samples when prepared |
Liquid samples in Example 2 |
Liquid samples in Comparative Example 2 |
| Dispersion liquid A |
9.98 % |
9.97 % |
5.66 % |
| Dispersion liquid B |
0.91 % |
0.88 % |
0.68 % |
| Dispersion liquid C1 |
0.44 % |
0.43 % |
0.32 % |
[0154] Next, each photoreceptor sample prepared in Examples 1 and 2,and Comparative Examples
1 and 2 was equipped with a copier model No. MF200 from Ricoh Company, Ltd., and the
initial copy image was evaluated using a test chart. Further, the copy image after
a durability test in which 10,000 copies were produced was evaluated.
[0155] The results are shown in Table 3.
[0156] Both the initial copy images and the copy images after the durability test were good
when using the photoreceptors prepared in Examples 1 and 2.
[0157] However, when using the photoreceptors prepared in Comparative Examples 1 and 2,
even the initial copy images had low and irregular image density. In addition, the
copy images after the durability test had lower image density, and background fouling
as well.
Table 3
| Image Evaluation Results |
| |
Initial |
After durability test in which 10,000 copies were produced |
| Example 1 |
Good |
Good |
| Comparative Example 1 |
Low and irregular image density |
Lower image density and background fouling |
| Example 2 |
Good |
Good |
| Comparative Example 2 |
Low and irregular image density |
Lower image density and background fouling |
[0158] This document claims priority and contains subject matter related to Japanese Patent
Applications Nos. 2001-003860, 2001-131076 and 2001-368911, filed on January 11, 2001,
April 27, 2001 and December 3, 2001 respectively, incorporated herein by reference.