BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to a method and an apparatus for washing a substrate.
Particularly, the present invention relates to a method and apparatus for washing
a substrate of an electrophotographic photoreceptor before forming a photosensitive
layer thereon.
Discussion of the Background
[0002] As the method for manufacturing a cylindrical substrate for an electrophotographic
photoreceptor, a method in which a substrate is prepared by ironing, cold drawing
or the like, and a method in which a substrate which is obtained by ironing, cold
drawing or the like is turned, are typically used.
[0003] However, a high viscosity oil used during the plastic forming process of the substrate,
which is obtained by the above-mentioned ironing or cold drawing method adheres on
the substrate. In addition, a turning oil used during the turning process adheres
on the substrate.
[0004] An electrophotographic photoreceptor is manufactured by coating a coating liquid
including a photosensitive material on an outer circumference of an electroconductive
substrate, resulting in formation of a photosensitive layer on the outer circumference
of the substrate. When the photosensitive layer is formed by dipping a substrate,
on which oils, foreign materials or the like are adhered, in a coating liquid, the
coating liquid is polluted with the oils, foreign materials or the like adhered on
the substrate, resulting in deterioration of the coating liquid, and thereby a photosensitive
layer having a desired characteristic cannot be formed. In addition, coating defects
such as uneven coating are formed due to the oils and foreign materials. Therefore,
the substrate is necessary to be washed before the coating liquid including a photosensitive
material is coated on the outer circumference thereof.
[0005] Recently, halogenated hydrocarbon solvents which have been used for washing a substrate
are hardly used in order to prevent occurrence of environmental problems such as ozone
depletion, warming of the earth, air pollution, and problems concerning human bodies.
[0006] Published unexamined Japanese Patent Application Nos. 6-118663 discloses a method
for washing a substrate with water including a surfactant using ultrasound. However,
a large quantity of surfactant has to be added to the washing liquid to obtain good
washing effect and in addition a long period of time is necessary to remove the surfactant
from the substrate.
[0007] Published unexamined Japanese Patent Application Nos. 9-6031 discloses a method for
washing a substrate using a brush. However, the brush often damages the surface of
the substrate.
[0008] Published unexamined Japanese Patent Application Nos. 2000-225381 discloses a method
for washing a substrate using an alkaline solution. However, when the alkaline solution
is prepared, there is a problem in handling because a strong alkali has to be used
when preparing the alkali solution. In addition, it is not easy to remove such a strong
alkali from the substrate.
SUMMARY OF THE INVENTION
[0009] Accordingly, an object of the present invention is to provide a method and an apparatus
for washing a substrate of an electrophotographic photoreceptor, wherein oils adhered
on a surface of a substrate is removed without damaging the substrate.
[0010] Another object of the present invention is to provide a washing liquid without a
dangerous operation such as handling a strong alkali material.
[0011] To achieve such objects, the present invention contemplates the provision of a method
for washing a substrate of an electrophotographic photoreceptor including degreasing
the substrate with a washing liquid; then rinsing the substrate with pure water; and
then drying the substrate, wherein the washing liquid is alkaline ionized water having
a temperature of from 20 °C to 90 °C.
[0012] It is preferable that an external force is applied to the substrate in order to improve
the washing effect of the alkaline ionized water.
[0013] In addition, it is preferable that the external force is applied using supersound
and/or a brush.
[0014] Further, it is preferable that the substrate is oscillated while the substrate is
dipped in the alkaline ionized water.
[0015] Furthermore, it is preferable that a bubble having a diameter of from 5 mm to 100
mm is insufflated onto the substrate in the rinsing process.
[0016] It is preferable that the quantity of air used for generating bubbles is from 10
L/minute to 80 L/minute.
[0017] It is preferable that in the drying process, the substrate is dipped into pure water
heated at a temperature of from 60 °C to 95 °C to be heated and then taken out of
the pure water to dry water adhered to the surface of the substrate._
[0018] It is preferable that the pure water has a resistivity not less than 1MΩ · cm.
[0019] It is preferable that the drawing speed of the substrate in the drying process is
from 3 to 20mm/second.
[0020] As another aspect of the present invention, an apparatus for washing a substrate
for an electrophotographic photoreceptor including:
a washing container configured to contain a washing liquid to wash the substrate;
a heater configured to heat the washing liquid to a temperature of from 20 °C to 90
°C;
a rinsing container configured to contain water or pure water to rinse the washed
substrate;
a warming container configured to contain warm pure water to warm the rinsed substrate;
a holder configured to support the substrate; and
a lifter configured to up and down the substrate and oscillate the substrate.
[0021] 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 drawing.
BRIEF DESCRIPTION OF THE DRAWING
[0022] Figure is a schematic diagram illustrating an example of the washing apparatus of
the present invention.
DETAILED DESCRIPTION OF THE INVENTION
[0023] Various lubricants used in the manufacturing processes of a substrate for an electrophotographic
photoreceptor are strongly adhered onto the substrate to an extent such that the lubricating
property of the lubricants does not deteriorate even when the lubricants are brought
into contact with a cutter or a die, i.e. , such that the oil slick formed on the
substrate is not easily removed.
[0024] In the present invention, it becomes possible to remove the lubricants adhered strongly
on the substrate without damaging the substrate by using alkaline ionized water while
properly adjusting the temperature of the alkaline ionized water and applying an external
force to the substrate.
[0025] The method of the present invention including degreasing the substrate with a washing
liquid; then rinsing the substrate with pure water; and then drying the substrate,
wherein the washing liquid is alkaline ionized water having a temperature of from
20 °C to 90 °C.
[0026] The lubricants adhered strongly on the substrate can be removed by using this method.
[0027] The washing method of the present invention includes the following processes.
(A) Washing process
[0028] As illustrated in Figure, a substrate 4 is transferred from a previous process by
a slider 6, and dipped into a washing container 1 containing alkaline ionized water
9 by a lifter 7 to degrease the substrate 4. When the substrate 4 is degreased, the
substrate 4 is drawn up by the lifter 7. Numeral 14 denotes a substrate holder. Numeral
5 denotes ultrasonic oscillators serving as an external force applier and configured
to apply an ultrasound to the washing liquid 9.
[0029] The alkaline ionized water 9, which is circulated between the washing container 1
and a reservoir container R
1 through passages C
1 and C
1', is preferably heated by a heater H
1 so as to effectively act on oils and the like materials adhered on the substrate
4. The oils removed from the substrate and mixed with the alkaline ionized water 9
are separated from the alkaline ionized water by a separator 8.
[0030] In addition, the alkaline ionized water 9 is circulated between the reservoir container
R
1 and the separator 8 through passages T
1 and T
1'. A pump P
1 and a filter F
1 are provided at a position of the passages T
1.
(B) Rinsing process
[0031] The substrate 4 is transferred from the washing process to the rinsing process by
the slider 6, and dipped into a rinsing container 2 containing pure water 12 by the
lifter 7. Pure water 12 in a reservoir container R
2 is poured into the rinsing container 2 containing pure water 12 to remove the alkaline
ionized water adhered on the substrate 4. Numeral 11 denotes bubbles which are generated
for effectively rinsing the substrate 4 . Numeral 10 denotes nozzles configured to
blow airs to form the bubbles 11. Numeral 15 denotes an air blower configured to blow
air to generate the bubbles 11.
[0032] In addition, the pure water 12 is circulated between the rinsing container 2 and
the reservoir container R
2 through passages T
2 and C
2. A pump P
2 and a filter F
2 are provided at a position of the passages T
2.
(C) Drying process
[0033] The substrate 4 is transferred from the rinsing process to the drying process by
the slider 6, and dipped into the warming container 3 containing warm pure water 13
by the lifter 7 to heat the substrate 4. The heated substrate is drawn up from the
warm pure water 13 and water adhered thereon is naturally dried because the substrate
4 is heated.
[0034] In addition, the warm pure water 13 is circulated between the warming container 3
and the reservoir container R
3 through passages T
3 and C
3. A pump P
3 and a filter F
3 are provided at a position of the passages T
3. Character H
3 denotes a heater configured to heat the pure water 13.
[0035] Hereinafter, each process will be explained in detail.
(A) Washing process
[0036] The temperature of the alkaline ionized water for use in the present invention is
preferably from 20 °C to 90 °C, more preferably from 30 °C to 80 °C, and even more
preferably from 40 °C to 60 °C.
[0037] Alkaline ionized water having too low temperature produces a low effect, to the contrary,
alkaline ionized water having too high temperature does not function as the alkaline
ionized water. It is possible to cleanly remove the oils adhered on a substrate for
an electrophotographic photoreceptor when the temperature of the alkaline ionized
water is properly controlled.
[0038] Alkaline ionized water is known as reduced water or super alkaline ionized water.
[0039] Alkaline ionized water is explained in detail in page 95 "MIZU NO HYAKKAJITEN (encyclopedia
of water)" published by Maruzen Co., Ltd. under the editorship of Takahashi, et al.
[0040] Specifically, alkaline ionized water is prepared as follows. An electrolyte is dissolved
at a low concentration in water contained in a container in which an anode chamber
and a cathode chamber are formed by a diaphragm. When the water is electrolyzed, the
water showing alkalinity contained in the cathode chamber is the alkaline ionized
water.
[0041] Specific examples of the electrolyte include salts of alkali metals such as sodium
chloride, calcium chloride and salt of organic acid such as sodium lactate, calcium
lactate, etc.
[0042] The alkaline ionized water has a pH greater than 7. The pH thereof depends on the
quantity of the electrolyte added and the quantity of electricity applied during the
electrolysis.
[0043] Alkaline ionized water having a pH of from 8 to 11 is preferably used in the present
invention. As such alkaline ionized water, water in the cathode chamber maybe used
when the pH thereof falls in a range of from 8 to 11 during the electrolysis. Alternatively,
it is possible to use alkaline ionized water prepared by a method in which the electrolysis
is continued until the pH reaches a pH not less than 13, and then the resultant alkaline
ionized water is diluted with neutral water so as to have a pH of from 8 to 11.
[0044] Alkaline ionized water can effectively remove organic foreign materials such as oils
adhered on the surface of a substrate. In addition, inorganic foreign materials such
as aluminum powders, sand powders, etc. adhered on the surface of the substrate can
also be removed.
[0045] Alkaline ionized water having a pH less than 8 has poor washing ability. In addition,
a large sized facility is necessary when alkaline ionized water having a pH greater
than 13 is used.
[0046] As mentioned above, alkaline ionized water has an effect of removing oils, foreign
materials and the like adhered on a surface of a cylindrical substrate. In a case
of light adhesion of an organic material, the organic material can be removed by dipping
a cylindrical substrate into alkaline ionized water. However, good washing effect
can be obtained by applying a physical force to the substrate, for example, by performing
contact washing.
[0047] Specific examples of the method utilizing a physical force are a method in which
a temperature of alkaline ionized water is increased, a method in which ultrasound
is used when the substrate is dipped in alkaline ionized water, a method in which
a gas is injected in alkaline ionized water for bubbling and a method in which a brush,
a sponge and the like material are used for wiping the substrate.
[0048] In addition, the washing ability can be improved by oscillating the substrate in
the vertical direction while an external force is applied thereto utilizing ultrasonic
oscillators, bubbling, brushes, sponges or the like.
[0049] Hereinafter, the conditions of ultrasound utilized in the washing process will be
concretely explained.
[0050] When an ultrasound having a low frequency not greater than 40 kHz is used, a problem
which occurs is that fine turning burrs which are generated when a substrate is turned,
and fine defects which are generated in the longitudinal direction thereof by aluminum
foreign materials adhered on the substrate when the cylindrical substrate is subjected
to plastic forming tend to be raised. Therefore, the substrate is preferably washed
with a high frequency ultrasound oscillator having a frequency of from 100 kHz to
150 kHz, so that the surface of the substrate is not damaged.
[0051] When the material of the substrate is aluminum, various aluminum compositions can
be used. For example, aluminum alloys of A1000 group, aluminum alloys of A3000 group
and aluminum alloys of A6000 group can apply thereto, and other aluminum alloys can
apply without problems.
[0052] When the substrate to be washed is made of an aluminum alloy of A1000 group, the
strength of the applied ultrasound is preferably 20 percent lower than in the case
when other alloys are ultrasonically washed.
[0053] In addition, the washing method of the present invention can also be applied to washing
of a nickel seamless belt prepared by electroforming. In this case, the strength of
the ultrasound is preferably decreased.
[0054] The seamless belt materials are preferably washed using a high frequency ultrasonic
oscillator oscillating an ultrasound having a frequency of from 100 kHz to 150 kHz.
[0055] Oscillation of the substrate is performed in order to avoid uneven washing of the
ultrasonic irradiation, and length of the oscillation in the vertical direction is
preferably not less than 50 mm.
[0056] It is preferable that at least two ultrasonic oscillators 5, which are illustrated
in Figure, are arranged so as to be located in or in the vicinity of the washing container
1 containing alkaline ionized water while horizontally opposed to each other.
[0057] In addition, it is preferable that two ultrasonic oscillators are arranged such that
one of the at least two ultrasonic oscillators is dislocated in the vertical direction.
[0058] Further, it is preferable that the one of the two ultrasonic oscillators is dislocated
at an angle of from 3° to 15°.
[0059] Hereinafter, a case in which a brush is used for applying a physical force to the
substrate will be explained.
[0060] When the diameter of the pile of the brush contacting to the substrate is greater
than 1 mm, defects such as scratches are formed on a surface of the substrate when
the brush is strongly contacted thereto.
[0061] In addition, when the length of the pile is less than 3 mm, defects such as scratches
are formed on a surface of the substrate when the brush is strongly contacted thereto.
[0062] In contrast, when the length of the pile is too long, the ability of the brush to
remove a foreign material is low.
[0063] The density of the pile is preferably not less than 10 pieces/cm
2.
[0064] Specific examples of the materials for use as the pile include nylon, polypropylene,
rayon, polyester, polytetraphloroethylene type fluorocarbon resin, mixture thereof,
animal hairs and the like.
[0065] The number of rotations of the brush is determined depending on the diameter and
the rotating speed of the brush. When the rotating speed is too low, the ability of
the brush to remove foreign materials is low.
[0066] The brush and the substrate should rotate in the same direction. By rotating the
brush and the substrate in the same direction, the brush and the substrate have different
running directions at the contact region thereof, so that a good washing effect can
be obtained.
[0067] The rotating speed of the brush and the substrate at the contact region is preferably
not less than 5 m/minute.
[0068] In addition, when the brush is contacted with the substrate to wash the substrate,
the substrate or the brush is preferably oscillated in the axis direction of the substrate
to avoid uneven washing.
[0069] The washing effect can be improved by using a combination of ultrasound with a brush.
[0070] When the materials to be washed are remarkably dirty, it is effective to remove the
remarkable stains by a washing method using a known surfactant or the like material
before washing with alkaline ionized water. The quantity of the surfactant can be
decreased by combining the washing method using a known surfactant and the washing
method using alkaline ionized water compared to a case in which a known surfactant
or the like is used alone.
(B) Rinsing process
[0071] Next, the rinsing process performed in the rinsing container will be explained referring
to Figure. An object of the rinsing process is to remove the alkaline ionized water
adhered on the substrate in the washing process performed in the washing container.
[0072] Water or pure water is suitably used as the rinsing liquid in the rinsing process.
[0073] As the rinsing method, ultrasonic rinsing with an ultrasonic oscillator, and bubbling
rinsing using bubbles are suitable. Among these methods, the bubbling rinsing is advantageous,
when the amount of capital investment is taken into consideration.
[0074] When forming bubbles 11, having a diameter of from 5 mm to 100 mm are preferably
used. Bubbles having a size of less than 5 mm and greater than 100 mm are inferior
in rinsing ability. The size of the bubbles 11 can be adjusted by changing the quantity
of blown air (i.e., the air pressure). When the air pressure is greater than 0.1 Mpa,
bubbles are united, resulting in formation of large bubbles having a size not less
than 10 mm.
[0075] Therefore the air pressure is preferably not greater than 0.1 Mpa, and more preferably
from 0.03 Mpa to 0.07 Mpa, in order to form bubbles having a size of from 3 mm to
5 mm.
[0076] In addition, the quantity of blown air used for generating the bubbles is from 10
L/minute to 80 L/minute, preferably from 20 L/minute to 60 L/minute, and more preferably
from 40 L/minute to 50 L/minute.
[0077] When the blown air is less than 10 L/minute, the number of the generated bubbles
is small. In contrast, when the blown air is greater than 80 L/minute, the volume
of the blown air is so large that the rinsing ability deteriorates.
[0078] It is preferable to provide at least two air-blowing nozzles to generate bubbles
for one substrate.
[0079] It is preferable to use a circular or plate-form sintered ceramic or sintered plastic
porous material as the nozzles 10.
[0080] Bubbles of uniform size are obtained when a sintered ceramic porous material or a
sintered plastic porous material are used.
[0081] The average pore diameter of the porous material is preferably not greater than 100
µm, and more preferably from 30 µm to 60 µm.
[0082] The bubbles generated by the nozzles 10 rise along the surface and the inside of
the substrate while removing the remaining washing liquid and foreign materials. The
rinsing effect is high when the diameter of the bubbles 11 is not greater than 10
mm. The bubbles 11 preferably have a uniform size of not less than 3 mm and not greater
than 5 mm.
[0083] The air for use in generating bubbles preferably has a clean level not lower than
class 100, and more preferably not lower than class 10, in order not to mix foreign
materials such as dust, oils and the like with pure water 12.
[0084] When the average pore diameter of the nozzles 10 is greater than 100 µm, uniform
size bubbles of from 3 mm to 5 mm cannot be formed.
[0085] When a circular sintered ceramic porous material or a circular sintered plastic porous
material having a diameter greater than 50 mm is used as the nozzles 10, a large number
of bubbles are formed in the center portion of the porous material but a small number
of the bubbles are formed in the edge portions of the porous material, and thereby
uniform size bubbles cannot be generated from the nozzles 10.
[0086] In order to form bubbles uniformly, the diameter of the circular porous material
is preferably not greater than 50 mm, and more preferably from 25 mm to 35 mm. When
a plate-form sintered ceramic porous material or a sintered plastic porous material
is used, the size is preferably 50 mm square, and more preferably from 25 mm square
to 35 mm square.
[0087] It is preferable to arrange plural nozzles to correspond to the possible largest
size of the substrate 4. In this case, the bubbles 11 can be contacted with the surface
and inside of all kinds of substrates to be washed without changing the nozzles when
the kind of the substrates to be washed is changed.
[0088] The lifter 7 and the substrate holder 14 provided on the lifter 7 have an opening
in order not to disturb the bubbles 11 coming from the lower portion of the rinsing
container 2 to be contacted with a surface and inside of the substrate 4. The substrate
4 is oscillated in the vertical direction by the lifter 7 to agitate pure water around
the substrate 4, resulting in improvement of the rinsing effect.
(C) Drying process
[0089] Next, the drying process using warm pure water will be explained referring to Figure.
[0090] In this process, at first the substrate 4 is dipped into warm pure water 13 in the
warming container 3 to be heated up to the temperature of the pure water. Then the
substrate is drawn up at a certain speed. Since the substrate 4 is heated, the pure
water adhered on the circumferential surface of the substrate 4 can be easily evaporated
and dried.
[0091] The temperature of the pure water 13 is preferably from 60 °C to 95 °C, more preferably
from 70 °C to 80 °C, and even more preferably 75 °C ± 3 °C, considering a drying speed
and a change of a state of a surface of the substrate.
[0092] When the temperature of the pure water 13 is less than 70 °C, a drying spot will
be formed on the surface of the substrate 4 even after the pure water adhered to the
surface of the substrate 4 is evaporated.
[0093] In addition, when the substrate 4 is dipped into the warm pure water 13 having a
resistivity less than 1 MΩ·cm, a hydroxide layer tends to be formed on the surface
of the substrate 4. It is not preferable for the substrate 4 to have such a hydroxide
layer because the layer affects the electric property of a photosensitive layer which
is to be formed thereon.
[0094] In addition, the drawing speed of the substrate 4 from the warm pure water 13 is
preferably from 3 to 20 mm/second.
[0095] When the speed is faster than 20 mm/second, a large quantity of water is adhered
on the substrate, and the substrate 4 is hard to dry.
[0096] The washing method of the present invention can also be applied for washing the substrates
other than the above-mentioned aluminum-alloy-based substrate. For example, the washing
method can also be applied to a washing a nickel seamless belt prepared by electroforming,
and nickel sulfamate and the like compounds remaining thereon can be removed.
[0097] In addition, the washing method can be effectively used for washing a synthetic polymer
substrate, and releasing agents remaining thereon can be effectively removed.
[0098] Further, the size of an object (substrate) to be washed is not limited as long as
the object can fit into the washing, rinsing and warming containers.
[0099] 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.
EXAMPLES
(Example 1)
[0100] An A3100 aluminum-alloy-based tube having an outer diameter of 100.7 mm, an inner
diameter of 97.5 mm and a length of 360 mm was prepared by drawing processing. The
tube was turned with a turning machine using a polycrystalline diamond as a turning
tool, so that the outer diameter becomes 100 mm. (Hereinafter, this tube is referred
to as a substrate)
[0101] In this case, kerosene was used as a turning oil, and the substrate was turned with
spraying kerosene to the turning portion. Therefore, a small quantity of kerosene
was adhered on the surface of the substrate.
[0102] A contact washing was performed five times with a washing apparatus as illustrated
in Figure using alkaline ionized water having a pH of 10.8 as a washing liquid.
<Conditions of washing apparatus>
Washing process
[0103] Temperature of alkaline ionized water: 50 °C
Rinsing process
No bubbles
[0104] Drying process
Temperature of pure water: 70 °C
Resistivity: 1.5 MΩ·cm
Drawing speed: 10 mm/second
[0105] The substrate was washed twice with tap water, rinsed with pure water three times,
and then dried after dipped into the warm pure water.
[0106] The following components were dispersed with a ball mill for 12 hours to prepare
an undercoat layer coating liquid.
Formation of undercoat layer
[0107]
Preparation of undercoat layer coating liquid |
Alkyd resin (BEKKOZOL 1307-60-EL from Dainippon Ink & Chemicals, Inc.) |
10 parts |
Methyl ethyl ketone |
150 parts |
Titanium oxide powder (CR-EL from Ishihara Sangyo Kaisha, Ltd.) |
90 parts |
[0108] The undercoat layer coating liquid was coated on the washed substrate by a dip coating
method, and then dried at 140 ° C for 20 minutes. Thus, an undercoat layer having
a thickness of 4.5 µm was formed.
[0109] When the condition of the undercoat layer formed on the substrate was observed with
naked eyes, a coating defect or any unevenly coated portion was not found.
Formation of charge generation layer (photosensitive layer)
Preparation of charge generation layer coating liquid
[0110] Next, the following components were dispersed in a ball mill for 48 hours.
Polyvinyl butyral resin (S-LEC BL-S manufactured by Sekisui Chemical Co., Ltd.) |
4 parts |
Methyl ethyl ketone |
10 parts |
[0111] Charge generation material having the following formula:

[0112] Further, 210 parts of methyl ethyl ketone was added thereto and dispersed for 3 hours.
[0113] After the mixture was dispersed in a ball mill, the mixture was transferred to a
container. The mixture was diluted with methyl ethyl ketone, so as to have a solid
content of 1.5 %. In addition, a polyether-modified silicone oil having a viscosity
of 120 cs (hydrophilic silicone oil SH-3746 manufactured by Dow Corning Toray Silicone
Co., Ltd.) was added in an amount of 0.02 % based on the total weight of the liquid
to prepare a charge generation layer coating liquid.
[0114] The charge generation layer coating liquid was coated on the substrate including
the undercoat layer by a dip coating method, and then dried at 130 °C for 20 minutes.
Thus, a generation layer having a thickness of 0.2 µm was formed.
[0115] When the film condition of the thus prepared charge generation layer was observed
with naked eyes, any coating defect or any unevenly coated portion was not found.
Formation of charge transport layer (photosensitive layer) Preparation of charge transport layer coating liquid
[0116] Ten (10) parts of a Z-form polycarbonate resin having 40,000 of viscosity average
molecular weight were dissolved in 85 parts of methylene chloride, and 9 parts of
a charge transport material having the below-mentioned formula (2) were added thereto
to be dissolved therein . Thus , a charge transport layer coating liquid was prepared.

[0117] The charge transport layer coating liquid was coated on the charge generation layer
formed overlying the substrate by a dip coating method, and then dried at 130 °C for
20 minutes. Thus, a charge transport layer having a thickness of 20 µm was formed.
[0118] When the film condition of thus prepared charge transport layer was observed with
naked eyes, a coating defect or an unevenly coated portion was not found.
[0119] Thus, an electrophotographic photoreceptor was prepared.
(Image formation and evaluation)
[0120] Flanges were attached at both edges of the thus prepared electrophotographic photoreceptor.
Then the photoreceptor was set in an Imagio MF-6550 to print half tone images. The
print images were observed to evaluate the image qualities. As a result, any abnormal
image was not produced and the print images have good image qualities.
(Example 2)
[0121] The procedure for preparation and evaluation of the photoreceptor in Example 1 was
repeated except that a brush on which a pile having a diameter of 0.1 mm, and a length
of 20 mm is provided at a density of 30 pieces/cm
2 was used for rubbing the substrate in the washing process. The resultant print images
have good image qualities.
[0122] The washing time was the same as that in Example 1. As a result of the observation
of the washing process, this method could remove stains faster than the method in
Example 1.
(Example 3)
[0123] The procedure for preparation and evaluation of the photoreceptor in Example 1 was
repeated except that an ultrasound of 100 kHz irradiated the substrate in the washing
process. The resultant print images have good image qualities.
[0124] The washing time was the same as that in Example 1. As a result of the observation
of the washing process, this method could remove stains faster than the method in
Example 1.
(Example 4)
[0125] The procedure for preparation and evaluation of the photoreceptor in Example 1 was
repeated except that bubbles having a diameter of 120 mm were applied to the substrate
by blowing air at a flow rate of 50 L/minute. The resultant print images have good
image qualities.
[0126] The washing time was the same as that in Example 1. As a result of the observation
of the washing process, this method could remove stains faster than the method in
Example 1.
(Example 5)
[0127] The procedure for preparation and evaluation of the photoreceptor in Example 1 was
repeated except that bubbles having a diameter of 50 mm were applied to the substrate
by blowing air at a flow rate of 50 L/minute. The resultant print images have good
image qualities.
[0128] The washing time was the same as that in Example 4. As a result of the observation
of the washing process, this method could remove stains faster than the method in
Example 4.
(Comparative Example)
[0129] The procedure for preparation of the A3100 aluminum-alloy-based tube in Example 1
was repeated.
[0130] Next, the procedure for washing the substrate in Example 1 was repeated except that
a washing liquid in which a surfactant "SUNWASH FM-950" manufactured by Lion Corp.
was diluted with water so that the mixture has a pH of 10.8 was used in the washing
process.
[0131] Next, the procedure for preparation of the undercoat layer in Example 1 was repeated.
Thus, an undercoat layer having a thickness of 4.5 µm was formed on the above-prepared
substrate.
[0132] The undercoat layer formed on the substrate was observed with naked eyes, several
circular coating defects in which the coating liquid were repelled were found.
[0133] Next, the procedure for preparation of the charge generation layer in Example 1 was
repeated. Thus, a charge generation layer having a thickness of 0.2 µm was formed.
[0134] The thus prepared charge generation layer was observed with naked eyes, several coating
defects in which the amount of the charge generation layer coating liquid adhered
on the circular coating defects on the undercoat layer was small (i.e., the coating
defects of the undercoat layer repelled the charge generation layer coating liquid).
[0135] Next, the procedure for preparation of the charge transport layer in Example 1 was
repeated. Thus, a charge transport layer having a thickness of 20 µm was formed.
[0136] The thus prepared charge transport layer was observed with naked eyes, coating defects
in which the coating liquid was repelled were found.
[0137] Thus a comparative electrophotographic photoreceptor was prepared.
[0138] Finally, flanges were attached at both edges of the thus prepared electrophotographic
photoreceptor. Then the photoreceptor was set in an Imagio MF-6550 to print half tone
images. The print images were observed to evaluate the image qualities. As a result,
undesired images were formed, which correspond to the coating defects of the photoreceptor.
[0139] It is found that alkaline ionized water itself can remove oils adhered on a substrate,
and, oils and the like materials can be effectively removed by using additionally
an ultrasound and a brush to apply an external force to the substrate.
[0140] This document claims priority and contains subject matter related to Japanese Patent
Applications No. 2003-031951 filed on February 10, 2003, No. 2002-262378, filed on
September 9, 2002 and No. 2002-136130, filed on May 10, 2002, incorporated herein
by reference.