BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to a roller member used for electrophotography, a process
cartridge using the roller member and an electrophotographic image forming apparatus
(hereinafter, referred to as an "electrophotographic apparatus") using the roller
member.
Description of the Related Art
[0002] An electrophotographic apparatus adopting an electrophotographic method is mainly
composed of an electrophotographic photosensitive member (hereinafter, may be simply
referred to as a "photosensitive member"), a charging device, an exposure device,
a developing device, a transfer device and a fixing device. The roller member is suitably
used in the charging device, the developing device, the transfer device and the fixing
device. In the charging device, the roller member is disposed in contact with or close
to the surface of the photosensitive member, and charges the surface of the photosensitive
member electrically by the applying of a voltage (a voltage only of a direct-current
voltage or a voltage of a direct-current voltage with an alternating-current voltage
superposed thereon).
[0003] Japanese Patent Application Laid-Open No.
2008-276026 discloses a charging roller having protrusions derived from electroconductive resin
particles, as a roller member (hereinafter, referred to as a "charging roller") for
charging a photosensitive member electrically in such a way that the roller member
is brought into contact with the photosensitive member.
[0004] However, in the charging roller according to Japanese Patent Application Laid-Open
No.
2008-276026, when the charging roller comes into contact with the photosensitive member, pressure
is concentrated on the protrusions derived from the resin particles, to result in
non-uniform abrasion of the surface of the photosensitive member in use over a long
term.
[0005] For such a problem, Japanese Patent Application Laid-Open No.
2011-237470 discloses a roller member including bowl-shaped resin particles having openings in
the electroconductive resin layer thereof and having on the surface thereof a concave-convex
shape derived from the openings and edges of the bowl-shaped resin particles. The
roller member according to Japanese Patent Application Laid-Open No.
2011-237470 is described to be capable of suppressing the non-uniform abrasion of the photosensitive
member even in use over a long term, due to the alleviation of the contact pressure
as a result of the elastic deformation at the time when the edges of the bowl-shaped
resin particles come into contact with the photosensitive member.
[0006] In the roller member according to Japanese Patent Application Laid-Open No.
2011-237470, the elastic deformation of the edges of the openings of the bowl-shaped resin particles
alleviates the pressure of contact between the edges and the photosensitive member.
For the above-described reason, the non-uniform abrasion of the surface of the photosensitive
member is suppressed even in use of the photosensitive member over a long term. On
the other hand, in the roller member according to Japanese Patent Application Laid-Open
No.
2011-237470, there is a possibility that the performance of rotation of the roller member following-up
the rotation of the photosensitive member (hereinafter, may be referred to as "follow-up
rotation performance") is degraded.
[0007] Recently, with increase in process speed of electrophotographic apparatuses, there
has been found a tendency such that when an electrophotographic image is formed, the
photosensitive member involved tends to vibrate. When the photosensitive member in
a state of vibration is to be charged by bringing a roller member which is low in
the follow-up rotation performance into contact with the photosensitive member, the
roller member may not follow-up the rotation of the photosensitive member to consequently
cause such a phenomenon (hereinafter, also referred to as "stick-slip") that the roller
member slips on the surface of the photosensitive member. The occurrence of the stick-slip
causes charging unevenness on the photosensitive member to cause the occurrence of
horizontal-line-like density unevenness on the electrophotographic image. Hereinafter,
the horizontal-line-like density unevenness occurring on the electrophotographic image
may be referred to as "banding." Additionally, an electrophotographic image on which
the horizontal-line-like density unevenness occurs may be referred to as a "banding
image."
SUMMARY OF THE INVENTION
[0008] Accordingly, the present invention is directed to providing a roller member capable
of sufficiently suppressing the non-uniform abrasion of the photosensitive member
and the occurrence of a banding image even in use over a long term. Also, the present
invention is directed to providing a process cartridge and an electrophotographic
apparatus conducive to the formation of high-quality electrophotographic images.
[0009] According to an aspect of the present invention, there is provided a roller member
for electrophotography comprising: an electroconductive substrate and an electroconductive
elastic layer as a surface layer;
wherein
the electroconductive elastic layer has a crown shape of which an outer diameter at
the middle of the roller member in the lengthwise direction is larger than those at
both ends of the roller member;
the electroconductive elastic layer comprises a binder and a bowl-shaped resin particle;
the surface of the roller member has a concavity derived from an opening of the bowl-shaped
resin particle and a protrusion derived from an edge of the opening of the bowl-shaped
resin particle; and
wherein the relation in the restoring rate of the roller member for elastic deformation
between at the middle of the roller member in the lengthwise direction and at both
ends of the roller member is such that:
on the surface of the electroconductive elastic layer, the restoring rate is larger
at the both ends than that at the middle, and
at the position of depth t µm from the surface of the electroconductive elastic layer,
the restoring rate is larger at the middle than that at the both ends.
[0010] According to another aspect of the present invention, there is provided a process
cartridge comprising the above roller member for electrophotography and an electrophotographic
photosensitive member, and being constituted to be demountable from the body of an
electrophotographic apparatus.
[0011] According to a further aspect of the present invention, there is provided an electrophotographic
apparatus comprising the above roller member for electrophotography and an electrophotographic
photosensitive member.
[0012] Further features of the present invention will become apparent from the following
description of exemplary embodiments with reference to the attached drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0013]
FIGS. 1A, 1B, 1C and 1D are diagrams illustrating the development of the effects of
the roller member according to the present invention.
FIGS. 2A and 2B are diagrams illustrating the development of the effects of the roller
member according to the present invention.
FIGS. 3A and 3B are cross-sectional views of the roller member according to the present
invention.
FIGS. 4A and 4B are partial cross-sectional views of the vicinity of the surface of
the roller member according to the present invention.
FIG. 5 is a partial cross-sectional view of the vicinity of the surface of the roller
member according to the present invention.
FIGS. 6A, 6B, 6C, 6D and 6E are diagrams illustrating the shapes of bowl-shaped resin
particles according to the present invention.
FIG. 7 is a diagram illustrating an electron beam irradiation apparatus used for the
production of the roller member according to the present invention.
FIG. 8 is a diagram illustrating a scanning electron beam irradiation source used
for the production of the roller member according to the present invention.
FIG. 9 is a diagram illustrating an area-type electron beam irradiation source used
for the production of the roller member according to the present invention.
FIG. 10 is a schematic cross-sectional view illustrating an example of the electrophotographic
apparatus according to the present invention.
FIG. 11 is a schematic cross-sectional view illustrating an example of the process
cartridge according to the present invention.
FIG. 12 is an example of a load-displacement curve for the roller member according
to the present invention.
DESCRIPTION OF THE EMBODIMENTS
[0014] Preferred embodiments of the present invention will now be described in detail in
accordance with the accompanying drawings.
[0015] The roller member for electrophotography according to the present invention (hereinafter,
may be simply referred to as a "roller member") has an electroconductive substrate
and an electroconductive elastic layer. The electroconductive elastic layer has a
crown shape of which an outer diameter at the middle of the roller member in the lengthwise
direction is larger than those at the both ends of the roller member.
[0016] The electroconductive elastic layer includes a binder resin and a bowl-shaped resin
particle. The surface of the roller member has a concavity derived from an opening
of the bowl-shaped resin particle and a protrusion derived from an edge of the opening
(hereinafter, sometimes simply referred to as "edge") of the bowl-shaped resin particle.
The relation in the restoring rate of the roller member for elastic deformation between
at the middle of the roller member in the lengthwise direction and at both ends of
the roller member in the lengthwise direction is such that: on the surface of the
electroconductive elastic layer, the restoring rate is larger at the both ends than
that at the middle, and at the position of depth t µm from the surface of the electroconductive
elastic layer, the restoring rate is larger at the middle than that at the both ends.
In present Specification, the restoring rate for the elastic deformation of the roller
member may be simply referred to as "restoring rate".
[0017] The protrusion derived from the edge more easily tend to undergo elastic deformation
when the roller member comes into contact with the photosensitive member as compared
to such protrusions due to the electroconductive resin particles as described in Japanese
Patent Application Laid-Open No.
2008-276026. Accordingly, the contact pressure is alleviated. FIG. 1A is an enlarged schematic
view of the close contact section (hereinafter, referred to as a "nip portion") between
the roller member including the bowl-shaped resin particles illustrated in FIGS. 4A
and 4B and the photosensitive member. In the nip portion, the contact pressure between
the edge and the photosensitive member elastically deforms the edge in the directions
of arrows A to result in alleviation of the contact pressure on the photosensitive
member. The foregoing effect enables the suppression of the non-uniform abrasion of
the photosensitive member even in use for an extended period of time.
[0018] On the other hand, the alleviation of the contact pressure may reduce the contact
area between the roller member and the photosensitive member, degrade the driven rotation
performance of the roller member in relation to the photosensitive member and cause
charging unevenness to occur on the photosensitive member. Such charging unevenness
can be a cause for the occurrence of banding images. Such a problem becomes more prominent
in the case where the process speed is more increased, and the vibration of the photosensitive
member becomes larger.
[0019] The roller member is disposed in relation to the photosensitive member driving the
roller member in such a way that the roller member is brought into contact with the
photosensitive member by applying a predetermined pushing pressure due to a spring
or the like to both ends of the roller member, and thus the roller member is follow-up
rotated with the rotation of the photosensitive member. In this case, if the roller
member is of a usual cylindrical shape, structurally, the pressurization in the middle
portion of the roller member comes to be weak, and there is a possibility of the occurrence
of the gap between the photosensitive member and roller member. On the basis of the
foregoing reason, for the purpose of bringing the roller member into contact with
the photosensitive member with a pressure uniform in the lengthwise direction of the
roller member, a roller member is suitably used which has a crown shape of which an
outer diameter at the middle of the roller member in the lengthwise direction is larger
than those at the both ends. By allowing the roller member to have a crown shape of
which an outer diameter at the middle of the roller member in the lengthwise direction
is larger than those at the both ends, the width of the close contact (hereinafter,
referred to as a "nip width") between the middle of the roller member and the photosensitive
member comes to be large, and hence the follow-up rotation performance in the middle
of the roller member in relation to the photosensitive member is improved. The follow-up
rotation performance is increasingly improved with the increase in the difference
in the outer diameter between the middle and the both ends.
[0020] However, in case of a great difference in the outer diameter between the middle and
the both ends in the lengthwise direction of the roller member, when the roller member
is followed-up rotated with the rotation of the photosensitive member, the circumferential
speed of the roller member comes to be larger at the both ends of the roller member
than at the middle. Consequently, a "twist" is exerted on the elastic layer of the
roller member, due to the difference in the circumferential speed between the middle
and the both ends in the lengthwise direction. Although such a "twist" is absorbed
by the elastic deformation to be caused in the elastic layer when the magnitude of
the twist is small, the "twist" is continuously accumulated in the elastic layer,
and when the accumulated twist exceeds a certain magnitude, the elastic layer takes
an action to get back to the original state so as to release the force of the "twist,"
resulting in the occurrence of the slip of the roller member. Specifically, the stick-slip
occurs at both end portions of the roller member. Consequently, charging unevenness
occurs partially on the photosensitive member to result in the occurrence of a banding
image.
[0021] For such a problem, the constitution of the roller member according the present invention
enables to establish the compatibility between the suppression of the non-uniform
abrasion of the photosensitive member and the suppression of the banding image due
to the improvement of the follow-up rotation performance of the roller member in relation
to the photosensitive member. The establishment of the compatibility is considered
to be due to the effects described in the following 1) and 2).
[0022] 1) The restoring rate of the elastic deformation of the electroconductive elastic
layer of the roller member according to the present invention becomes larger on the
surface of the electroconductive elastic layer, in the direction from the middle of
the roller member toward the both ends in the lengthwise direction.
[0023] The bowl-shaped resin particles formed on the surface of the electroconductive elastic
layer are in the state in which the edges 11 are elastically deformed due to the pressure
of contact with the photosensitive member 13 in the directions of the arrows A in
the nip portion as shown in FIG. 1A.
[0024] FIG. 1B is a schematic cross-sectional view of the nip portion. As shown in FIG.
1B, the roller member 14 is brought into contact with the photosensitive member 13
by a predetermined pushing pressure (not shown) due to, for example, a spring. Following
the rotation of the photosensitive member in the direction of an arrow B, the roller
member is driven to rotate in the direction of another arrow B. In this case, the
contact pressure exerted by the photosensitive member on the roller member is the
largest at the center (the position C) of the nip portion 15. Accordingly, the elastic
deformation of the edge also becomes large as shown in FIG. 1C. Consequently, the
contact area between the edge 11 and the photosensitive member surface is the largest
in the nip portion. Subsequently, when the resin particles move to the termination
(the position D) in the nip portion, the contact pressure exerting on the roller member
and the bowl-shaped resin particles is decreased and the contact pressure is released
when the resin particles depart from the nip portion. The state of the bowl-shaped
resin particles in this case is shown in FIG. 1D. Specifically, the elastic deformation
of the edge 11 is restored in the direction of an arrow E in FIG. 1D to reduce the
contact area between the edge and the photosensitive member. The present inventors
have discovered that the restoring rate of the elastic deformation of the edges 11
of the bowl-shaped resin particles due to the decrease and the release of the contact
pressure exerted on the bowl-shaped resin particles depends on the restoring rate
of the elastic deformation of the surface region of the electroconductive elastic
layer 12 holding the resin particles. Specifically, the present inventors have discovered
that the higher the restoring rate from the elastic deformation of the surface region
of the electroconductive elastic layer 12 is, the higher the restoring rate from the
elastic deformation of the edge portion of the bowl-shaped resin particles is.
[0025] Accordingly, for the surface region of the electroconductive elastic layer 12, the
present inventors have tried to make larger the restoring rate at both ends in the
lengthwise direction of the roller member as compared to the restoring rate in the
middle in the lengthwise direction of the roller member. As a result, the restoring
rate immediately after the passage of the edges of the bowl-shaped resin particles
through the nip portion is considered to become larger at both ends of the roller
member than at the middle in the lengthwise direction. Consequently, immediately after
the passage through the nip portion, the state of contact between the edges of the
bowl-shaped resin particles and the photosensitive member is as shown in FIG. 1D at
both ends in the lengthwise direction of the roller member and is as shown in FIG.
1A in the middle in the lengthwise direction of the roller member. The attainment
of such a state reduces, at both ends, the contact area between the protrusions derived
from the edges and the photosensitive member, and consequently, the frictional force
between the surface of the electroconductive elastic layer and the photosensitive
member is decreased at both ends as compared to in the middle. In this case, the force
of the "twist" due to the circumferential speed difference between the middle and
the both ends of the roller member comes to be hardly accumulated at both ends, in
the lengthwise direction, of the electroconductive elastic layer of the roller member.
The occurrence of the stick-slip to cause the charging unevenness can be considered
to be consequently suppressed.
[0026] On the other hand, the restoring rate of the elastic deformation of the edges of
the bowl-shaped resin particles is slower at the middle of the roller member in the
lengthwise direction than at the both ends to result in the suppression of the reduction
of the contact area between the protrusions of the surface of the roller member and
the photosensitive member immediately after the passage through the nip portion. Consequently,
the follow-up rotation performance of the roller member in relation to the photosensitive
member is maintained satisfactorily.
[0027] 2) The restoring rate of the elastic deformation at the position of a predetermined
depth t µm from the surface of the electroconductive elastic layer of the roller member
according to the present invention becomes larger in the direction from the both ends
of the roller member toward the middle in the lengthwise direction of the roller member.
[0028] As described in the foregoing 1), the restoring rate of the elastic deformation in
the surface region of the electroconductive elastic layer mainly contributes to the
state of contact between the edges of the bowl-shaped resin particles in the surface
of the roller member and the photosensitive member. On the contrary, the restoring
rate of the elastic deformation at the position of the predetermined depth t µm from
the surface is considered to contribute to the substantial nip width.
[0029] When the roller member 14 is driven to rotate following-up the rotation of the photosensitive
member 13, the contact pressure becomes maximum at the center (the position C) of
the nip portion 15 in FIG. 1B. The roller member is deformed by the contact pressure,
and hence the outer diameter of the roller member becomes minimum at the position
C. Subsequently, the contact pressure is decreased when the roller member rotates
to move to the termination (the position D in FIG. 1B) of the nip portion, and hence
the outer diameter of the roller member is restored. In the outermost termination
end region (the dotted-line frame F) of the nip portion in FIG. 2A, the restoration
of the outer diameter occurs in the direction of an arrow G in FIG. 2B. In the case
where the restoring rate of the outer diameter of the roller member in the outermost
termination end region is fast, the state in which the surface of the roller member
and the surface of the photosensitive member are in close contact with each other
continues over a longer period of time as compared to the case where the restoring
rate is slow. This effect works as if the nip width were increased.
[0030] In the roller member according to the present invention, the restoring rate of the
elastic deformation in the deep layer part of the electroconductive elastic layer,
namely, in the part of a depth of t µm from the surface is larger at the middle of
the roller member in the lengthwise direction than at the both ends. For the reason,
the restoring rate of the outer diameter of the electroconductive elastic layer in
the outermost termination end region of the nip portion is made faster at the middle
of the roller member in the lengthwise direction than at the both ends. Therefore,
the substantial nip width is larger at the middle than at the both ends. Consequently,
the number of the contact points at which the edges are in contact with the photosensitive
member is larger at the middle in the lengthwise direction of the roller member and
is smaller at the both ends. Specifically, the contact area between the protrusions
derived from the edges and the photosensitive member is larger at the middle and is
smaller at the both ends in the lengthwise direction of the roller member, and hence
the frictional force (grip property) between the middle in the lengthwise direction
of the roller member having a crown shape and the photosensitive member is improved.
Consequently, the follow-up rotation performance of the roller member in relation
to the photosensitive member can be improved.
[0031] Here, the restoring rate for the elastic deformation of the electroconductive elastic
layer in regard to the present invention is described. The restoring rate of the elastic
deformation of the electroconductive elastic layer according to the present invention
is determined by the following method. Specifically, by using a microhardness tester
based on the indentation test method according to ISO 14577 (Metallic materials-Indentation
test for hardness and material parameters), an indenter is made to sink in the electroconductive
elastic layer in a predetermined magnitude (D µm) by applying a load to the indenter.
Hereinafter, the predetermined magnitude may be referred to as "indentation depth."
Examples of the microhardness tester include "PICODENTER HM500" (trade name, manufactured
by Fischer Instruments KK).
[0032] Subsequently, the load applied to the indenter is unloaded, and the restored distance
(µm) of the elastic layer is calculated based on the force exerted on the indenter
by the elastic layer in the unloading step. Thus, as shown in FIG. 12, a graph is
obtained which shows the relations between the load (mN) applied to the indenter,
the indentation depth (µm) and the restored distance(µm) of the elastic layer at the
time of unloading.
[0033] When the restored distance of the elastic layer immediately after the start of the
unloading, more specifically, after 0.1 second from the start of the unloading is
represented by L µm, the restoring rate v (µm/sec) is found based on the following
calculation formula (1):

[0034] The reason for the use of the restored distance L after 0.1 second from the start
of the unloading in the calculation of the restoring rate is as follows. Specifically,
in the outermost termination end region of the nip portion, the restoring rate immediately
after the surface region of the electroconductive elastic layer is released from the
contact pressure is considered to control the restoring rate from the elastic deformation
of the edges of the bowl-shaped resin particles. Similarly, in the outermost termination
region of the nip portion, the restoring rate immediately after the deep layer region
of the electroconductive elastic layer is released from the contact pressure is considered
to control the substantial nip width. Accordingly, in the present invention, the restoring
rate immediately after the electroconductive elastic layer of the roller member is
released from the contact pressure, calculated by using the restored distance after
0.1 second from the start of the unloading of the electroconductive elastic layer,
is regarded as the restoring rate of the electroconductive elastic layer.
[0035] The surface region according the present invention is defined as the region of a
depth of 10 µm from the face of the electroconductive elastic layer opposite to the
face thereof facing the electroconductive substrate, that is, from the surface of
the electroconductive elastic layer. This is because the restoration from the elastic
deformation of the edges, described in 1), is considered to be substantially controlled
by the restoring rate of the electroconductive elastic layer in the region of a depth
of 10 µm from the surface of the electroconductive elastic layer. Accordingly, the
indentation depth D µm of the indenter of the microhardness tester is preferably set
to be 10 µm.
[0036] Additionally, in the present invention, the target value for the depth t µm from
the face of the electroconductive elastic layer opposite to the face thereof facing
the electroconductive substrate, that is, from the surface of the electroconductive
elastic layer, which depth defines the deep layer region of the electroconductive
elastic layer, is preferably 30 µm or more and 100 µm or less. By setting the value
of t µm so as to fall within this range, the effect of the increase of the substantial
nip width in the middle in the lengthwise direction of the roller member can be more
certainly achieved in a favorable manner. In other words, within this depth range,
the restoring rate of the electroconductive elastic layer is preferably larger at
the middle in the lengthwise direction of the roller member than at the both ends.
For that purpose, the indentation depth D µm in the measurement of the restoring rate
of the deep layer region of the electroconductive elastic layer according the present
invention is preferably set to be 20 to 100 µm.
<Roller Member>
[0037] Hereinafter, the roller member according the present invention is described in detail.
FIGS. 3A and 3B are schematic views of examples of the cross-sectional views of the
roller member according to the present invention. The roller member of FIG. 3A has
an electroconductive substrate 1 and an electroconductive elastic layer 2. As shown
in FIG. 3B, the electroconductive elastic layer may be a two-layered configuration
composed of electroconductive elastic layers 21 and 22. The electroconductive elastic
layers each include a binder, electroconductive fine particles and bowl-shaped resin
particles.
[0038] The electroconductive substrate and the electroconductive elastic layer, or layers
(such as electroconductive elastic layer 21 and electroconductive elastic layer 22
shown in FIG. 3B) sequentially laminated on the electroconductive substrate may be
allowed to adhere to each other through the intermediary of an adhesive. In this case,
the adhesive is preferably electroconductive. As the adhesive for electroconduction,
known adhesives can be used.
[0039] Examples of the binder of the adhesive include thermosetting resins and thermoplastic
resins; as the binder, heretofore known binders such as urethane-based, acrylic, polyester-based,
polyether-based, epoxy-based binders can be used.
[0040] An electroconductive agent to impart electroconductivity to the adhesive is appropriately
selected from the below-described electroconductive fine particles which can be used
to make the elastic layer electroconductive, and the selected electroconductive fine
particles can be used alone or in a combination of two or more.
[0041] The roller member according the present invention is preferably of a crown shape
in which the roller member is thickest at the middle in the lengthwise direction and
becomes thinner towards both ends of the roller member, from the viewpoint of improving
the follow-up rotation performance of the roller member at the middle in the lengthwise
direction in relation to the photosensitive member. A preferable range of the "crown
quantity" is from 30 to 200 µm. The crown quantity is the difference between the outer
diameter D2 at the middle in the lengthwise direction of the roller member and the
mean value of the outer diameters D1 and D3 at the positions separated by 90 mm from
the middle toward both ends; thus, the crown quantity is a value derived based on
the following calculation formula (2):

[Electroconductive Substrate]
[0042] The electroconductive substrate used for the roller member of the present invention
has electroconductivity and has a function to support the electroconductive elastic
layer or the like formed thereon. Examples of the materials of the substrate may include:
metals such as iron, copper, stainless steel, aluminum and nickel; and alloys of these
metals.
[Electroconductive Elastic Layer]
[0043] FIGS. 4A and 4B are partial cross-sectional views of the vicinity of the surface
of the electroconductive elastic layer of the roller member. A part of the bowl-shaped
resin particles 41 included in the electroconductive elastic layer is partially exposed
to the surface of the roller member. The surface of the roller member has the concavities
52 derived from the openings 51 of the bowl-shaped resin particles exposed to the
surface and the protrusions derived from the edges 53 of the openings of the bowl-shaped
resin particles exposed to the surface.
[0044] With reference to FIG. 5, the distance 54 between the top of the protrusion 53 derived
from the edge of the opening of the bowl-shaped resin particle and the bottom of the
concavity 52 demarcated by the shell of the bowl-shaped resin particle is preferably
set to be 5 µm or more and 100 µm or less and particularly preferably 8 µm or more
and 80 µm or less. Hereinafter, the foregoing distance may be referred to as "height
difference." The distance 54 set within the foregoing range more certainly enables
the alleviation of the contact pressure. The ratio between the height difference 54
and the maximum diameter 55 of the bowl-shaped resin particle, namely, [maximum diameter]/[height
difference] of the resin particle is preferably 0.8 or more and 3.0 or less. The foregoing
ratio set within the foregoing range more certainly enables the reduction of the above-described
contact pressure.
[0045] The formation of the foregoing concave-convex shape preferably controls as described
below the surface state of the roller member, namely, the surface state of the electroconductive
elastic layer. The ten-point average roughness (Rzjis) is preferably 5 µm or more
and 65 µm or less, in particular, 10 µm or more and 50 µm or less. The mean concave-convex
spacing (Sm) of the surface is preferably 30 µm or more and 200 µm or less, in particular,
40 µm or more and 150 µm or less. The adoption of the foregoing ranges more certainly
enables the reduction of the contact pressure. The measurement methods for the ten-point
average roughness (Rzjis) of the surface and the mean concave-convex spacing (Sm)
of the surface are described in detail below.
[0046] FIGS. 6A to 6E illustrate examples of the bowl-shaped resin particles used in the
present invention. In the present invention, the "bowl-shaped" particle means a particle
having an opening 61 and a roundish concavity 62 demarcated by a shell. The opening
may have a smooth edge as illustrated in FIG. 6A and FIG. 6B, or an uneven edge as
illustrated in FIG. 6C to FIG. 6E.
[0047] The maximum diameter 55 of the bowl-shaped resin particles is 5 µm or more and 150
µm or less, in particular, 8 µm or more and 120 µm or less. The ratio between the
maximum diameter 55 of the bowl-shaped resin particles and the minimum diameter 63
of the opening, namely, the ratio [maximum diameter]/[minimum diameter of opening]
of the bowl-shaped resin particles is preferably 1.1 or more and 4.0 or less. The
foregoing ratio set to fall within the foregoing range more certainly enables the
reduction of the above-described contact pressure.
[0048] The thickness of the shell of the bowl-shaped resin particles is preferably 0.1 µm
or more and 3 µm or less, in particular, 0.2 µm or more and 2 µm or less. The thickness
of the shell set to fall within this range enables more flexible elastic deformation
of the edge, and consequently, more certainly enables the alleviation of the contact
pressure. With respect to the thickness of the shell, the maximum thickness is preferably
three or less times the minimum thickness and more preferably two or less times the
minimum thickness.
[Binder]
[0049] As the binder included in the electroconductive elastic layer of the present invention,
heretofore known rubbers or resins can be used. Examples of the rubber include natural
rubber and natural rubber subjected to vulcanization, and synthetic rubbers. Examples
of the synthetic rubbers include the following: ethylene propylene rubber, styrene
butadiene rubber (SBR), silicone rubber, urethane rubber, isopropylene rubber (IR),
butyl rubber, acrylonitrile butadiene rubber (NBR), chloroprene rubber (CR), acrylic
rubber, epichlorohydrin rubber and fluororubber. Examples of the resins include resins
such as thermosetting resins and thermoplastic resins. Among these, fluororesin, polyamide
resin, acrylic resin, polyurethane resin, acrylic urethane resin, silicone resin and
butyral resin are more preferable. These may be used each type alone or as mixtures
of two or more types. Alternatively, the monomers which are the materials for these
binders may be copolymerized to be converted into copolymers.
[Electroconductive Fine Particle]
[0050] The electroconductive elastic layer includes heretofore known electroconductive fine
particles for the purpose of developing electroconductivity. Examples of the electroconductive
fine particles include metal oxides, metal fine particles and carbon black. These
electroconductive fine particles can be used each type alone or in combinations of
two or more types. The standard value of the content of the electroconductive fine
particles in the electroconductive elastic layer is 2 to 200 parts by mass, in particular,
5 to 100 parts by mass in relation to 100 parts by mass of the binder.
[Method for Forming Electroconductive Elastic Layer]
[0051] A method for forming the electroconductive elastic layer is exemplified as follows.
First, on the electroconductive substrate, a coating layer (hereinafter, referred
to as "preliminary coating layer") is prepared in which electroconductive fine particles
and hollow-shaped resin particles are dispersed in a binder. Subsequently, the hollow-shaped
resin particles are partially scraped away by polishing the surface of the particles
to form a bowl shape, and the concavities derived from the openings of the resulting
bowl-shaped resin particles and the protrusions derived from the edges of the openings
of the resulting bowl-shaped resin particles are formed. Hereinafter, the shape including
these concavities and protrusions is referred to as "concave-convex shape derived
from the openings of the bowl-shaped resin particles". In this way, the electroconductive
resin layer is formed, and then the surface of the electroconductive resin layer is
subjected to electron beam irradiation to control the restoring rate of the elastic
deformation of the electroconductive elastic layer.
[Dispersion of Resin Particles in Preliminary Coating Layer]
[0052] First, a method for dispersing the hollow-shaped resin particles in the preliminary
coating layer is described. Such a method can be exemplified by a method in which
a coating film of an electroconductive resin composition prepared by dispersing hollow-shaped
particles containing gas in the interior thereof together with the binder and the
electroconductive fine particles is formed on the electroconductive substrate, the
coating film is subjected to, for example, drying, curing or cross-linking. Examples
of the material used for the hollow-shaped resin particles may include the above-described
heretofore known resins.
[0053] Another method can be exemplified by a method which uses a so-called thermally expandable
microcapsule including an encapsulated substance in the interior of particles and
becoming hollow-shaped resin particles due to the expansion of the encapsulated substance
by heating. Specifically, this is a method in which an electroconductive resin composition
is prepared in which a thermally expandable microcapsule is dispersed together with
a binder and electroconductive fine particles, and then an electroconductive substrate
is coated with the prepared composition, and the composition coating is, for example,
dried, cured or cross-linked. In the case of this method, the hollow-shaped resin
particles can be formed by expanding the encapsulated substance with the heat at the
time of drying, curing or cross-linking of the binder used in the preliminary coating
layer. In this case, by controlling the temperature condition, the particle size can
be controlled.
[0054] When a thermally expandable microcapsule is used, a thermoplastic resin is required
to be used as the binder. Examples of the thermoplastic resin include the following:
acrylonitrile resin, vinyl chloride resin, vinylidene chloride resin, methacrylic
acid resin, styrene resin, urethane resin, amide resin, methacrylonitrile resin, acrylic
acid resin, acrylic acid ester resins and methacrylic acid ester resins. Among these,
it is preferable to use a thermoplastic resin including at least one selected from
acrylonitrile resin, vinylidene chloride resin and methacrylonitrile resin being low
in gas permeability and exhibiting high impact resilience. These thermoplastic resins
can be used each alone or in combinations of two or more thereof. Moreover, the monomers
being the raw materials for these thermoplastic resins may be copolymerized to produce
copolymers.
[0055] As the substance to be encapsulated in a thermoplastic microcapsule, a substance
is preferable which turns into gas and expands at a temperature equal to or lower
than the softening point of the thermoplastic resin. Examples of such a substance
include the following: low boiling point liquids such as propane, propylene, butene,
normal butane, isobutane, normal pentane and isopentane; and high boiling point liquids
such as normal hexane, isohexane, normal heptane, normal octane, isooctane, normal
decane and isodecane.
[0056] The thermally expandable microcapsule can be produced by heretofore known production
methods such as a suspension polymerization method, an interfacial polymerization
method, an interfacial sedimentation method and a liquid drying method. For example,
the suspension polymerization method can be exemplified by a method in which a polymerizable
monomer, a substance to be encapsulated in the thermally expandable microcapsule and
a polymerization initiator are mixed together, the resulting mixture is dispersed
in an aqueous medium including a surfactant and a dispersion stabilizer, and then
the mixture is allowed to undergo suspension polymerization. A compound having a reactive
group to react with a functional group of a polymerizable monomer, an organic filler
can also be added.
[0057] The polymerizable monomer can be exemplified by the following: acrylonitrile, methacrylonitrile,
α-chloroacrylonitrile, α-ethoxyacrylonitrile, fumaronitrile, acrylic acid, methacrylic
acid, itaconic acid, maleic acid, fumaric acid, citraconic acid, vinylidene chloride,
vinyl acetate; acrylic acid esters (methyl acrylate, ethyl acrylate, n-butyl acrylate,
isobutyl acrylate, t-butyl acrylate, isobornyl acrylate, cyclohexyl acrylate, benzil/benzyl
acrylate); methacrylic acid esters (methyl methacrylate, ethyl methacrylate, n-butyl
methacrylate, isobutyl methacrylate, t-butyl methacrylate, isobornyl methacrylate,
cyclohexyl (meth)acrylate, benzil/benzyl methacrylate); styrene-based monomers, acrylamide,
substituted acrylamide, methacrylic amide, substituted methacrylic amide, butadiene,
ε-caprolactam, polyether and isocyanate. These polymerizable monomers can be used
each alone or in combinations of two or more thereof.
[0058] As the polymerization initiator, an initiator soluble in the polymerizable monomer
is preferable, and heretofore known peroxide initiators and azo initiators can be
used. Among these, azo initiators are preferable. Examples of the azo initiator are
listed below: 2,2'-azobisisobutyronitrile, 1,1'-azobis(cyclohexane-1-carbonitrile)
and 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile). Among these, 2,2'-azobisisobutyronitrile
is preferable. When a polymerization initiator is used, the amount of the polymerization
initiator is preferably 0.01 to 5 parts by mass in relation to 100 parts by mass of
the polymerizable monomer.
[0059] As the surfactant, an anionic surfactant, a cationic surfactant, a nonionic surfactant,
an amphoteric surfactant and a polymeric dispersant can be used. The amount used of
the surfactant is preferably 0.01 to 10 parts by mass in relation to 100 parts by
mass of the polymerizable monomer.
[0060] Examples of the dispersion stabilizer include the following: organic fine particles
(such as polystyrene fine particle, polymethyl methacrylate fine particle, polyacrylic
acid fine particle and polyepoxide fine particle), silica (such as colloidal silica),
calcium carbonate, calcium phosphate, aluminum hydroxide, barium carbonate, and magnesium
hydroxide. The amount used of the dispersion stabilizer is preferably 0.01 to 20 parts
by mass in relation to 100 parts by mass of the polymerizable monomer.
[0061] The suspension polymerization is preferably conducted by using a pressure resistant
vessel under a sealed condition. The polymerization raw materials are suspended with,
for example, a disperser, then the resulting suspension is transferred into a pressure
resistant vessel and may be allowed to undergo suspension polymerization, or alternatively,
the suspension operation may be performed in the pressure resistant vessel. The polymerization
temperature is preferably 50°C to 120°C. The polymerization may be performed under
atmospheric pressure; however, in order to prevent the vaporization of the substance
to be encapsulated in the thermally expandable microcapsule, the polymerization is
preferably performed under a pressurized condition (under a pressure of atmospheric
pressure plus 0.1 to 1 MPa). After the completion of the polymerization, solid-liquid
separation and cleaning may also be performed by centrifugal separation or filtration.
When solid-liquid separation or cleaning is performed, subsequently, drying or crushing
may also be performed at a temperature equal to or lower than the softening temperature
of the resin constituting the thermally expandable microcapsule. Drying and crushing
can be performed by known methods; a flash dryer, a downwind dryer and a Nauta mixer
can be used. Drying and crushing can also be simultaneously performed with a crushing
dryer. The surfactant and the dispersion stabilizer can be removed by repeating cleaning
and filtration after production.
[Method for Forming Preliminary Coating Layer]
[0062] Successively, a method for forming the preliminary coating layer is described. Examples
of the method for forming the preliminary coating layer include a method in which
a layer of an electroconductive resin composition is formed on an electroconductive
substrate by an application method such as electrostatic spray application, dipping
application or roll application, and then, the layer is cured by drying, heating or
cross-linking. Alternatively, such examples also include a method in which a sheet-shaped
or tube-shaped layer, prepared by forming a film of the electroconductive resin composition
so as to have a predetermined thickness and by curing the film, is allowed to adhere
to the electroconductive substrate, or the substrate is coated with the resulting
layer. Additionally, the preliminary coating layer can also be formed by placing the
electroconductive resin composition in a mold with the electroconductive substrate
disposed therein, and then curing the composition. In particular, when the binder
is rubber, the preliminary coating layer can also be prepared, by using an extruder
equipped with a cross head die, and by integrally extruding the electroconductive
substrate and an unvulcanized rubber composition. Here, the cross head die is an extrusion
die used as disposed at the tip of the cylinder of an extruder for the purpose of
forming the coating layer of an electric wire or a wire.
[0063] Subsequently, after the drying, curing, cross-linking or the like, the surface of
the preliminary coating layer is polished to partially scrape away the hollow-shaped
resin particles to form bowl shapes. As the polishing method, a cylinder polishing
method and a tape polishing method can be used. A cylinder polishing machine can be
exemplified by a traverse type NC cylinder polishing machine and a plunge cut-type
NC cylinder polishing machine.
(a) Case Where the Thickness of Preliminary Coating Layer is Five or Less Times the
Average Particle Size of Hollow-Shaped Resin Particles
[0064] In the case where the thickness of the preliminary coating layer is five or less
times the average particle size of the hollow particles, the protrusions derived from
the hollow-shaped resin particles are often formed on the surface of the preliminary
coating layer. In this case, the protrusions of the hollow-shaped resin particles
are partially scraped away to form bowl shapes, and thus the concave-convex shape
due to the openings of the bowl-shaped resin particles can be formed. In this case,
it is preferable to use tape polishing in which the pressure exerted on the preliminary
coating layer at the time of polishing is relatively small. As an example, the preferable
ranges as the polishing conditions of the preliminary coating layer in the case where
a tape polishing method is adopted are presented below.
[0065] The polishing tape is a tape obtained by dispersing polishing abrasive grains in
a resin and by applying the resulting dispersion on a sheet-like substrate. The polishing
abrasive grain can be exemplified by aluminum oxide, chromium oxide, silicon carbide,
iron oxide, diamond, cerium oxide, corundum, silicon nitride, silicon carbide, molybdenum
carbide, tungsten carbide, titanium carbide and silicon oxide. The average particle
size of the polishing abrasive grain is preferably 0.01 µm or more and 50 µm or less
and more preferably 1 µm or more and 30 µm or less. The average particle size of the
polishing abrasive grain is the median diameter D50 measured by a centrifugal sedimentation
method. The preferable range of the grit number of the polishing tape having the polishing
abrasive grains falling within the foregoing preferable range is 500 or more and 20000
or less, and the more preferable range is 1000 or more and 10000 or less. Specific
examples of the polishing tape include the following: MAXIMA LAP and MAXIMA T type
(trade names, manufactured by Ref-Lite Co., Ltd.), Lapika (trade name, manufactured
by Kovax Corp.), Microfinishing Film and Lapping Film (trade names, manufactured by
Sumitomo 3M Ltd.), Mirror Film and Lapping Film (trade names, manufactured by Sankyo
Rikagaku Co., Ltd.), and Mipox (trade name, manufactured by Nihon Micro Coating Co.,
Ltd.).
[0066] The traveling speed of the polishing tape is preferably 10 mm/min or more and 500
mm/min or less and more preferably 50 mm/min or more and 300 mm/min or less. The press-on
pressure of the polishing tape to the preliminary coating layer is preferably 0.01
MPa or more and 0.4 MPa or less and more preferably 0.1 MPa or more and 0.3 MPa or
less. In order to control the press-on pressure, a backup roller may be allowed to
come into contact with the preliminary coating layer through the intermediary of the
polishing tape. In order to obtain an intended shape, the polishing treatment may
be performed over a plurality of times. The number of rotations is preferably set
at 10 rpm or more and 1000 rpm or less and more preferably 50 rpm or more and 800
rpm or less. By adopting the foregoing conditions, the concave-convex shape due to
the opening of the bowl-shaped resin particles can be more easily formed on the surface
of the preliminary coating layer. Even when the thickness of the preliminary coating
layer falls within the foregoing range, the concave-convex shape due to the opening
of the bowl-shaped resin particles can be formed by the method described below in
(b).
(b) Case Where the Thickness of Preliminary Coating Layer Exceeds Five Times the Average
Particle Size of Hollow-Shaped Resin Particles
[0067] In the case where the thickness of the preliminary coating layer exceeds five times
the average particle size of the hollow-shaped resin particles, a case occurs in which
no protrusions derived from the hollow-shaped resin particles are formed on the surface
of the preliminary coating layer. In such a case, by taking advantage of the polishability
difference between the hollow-shaped resin particles and the preliminary coating layer,
the concave-convex shape due to the opening of the bowl-shaped resin particles can
be formed. The hollow-shaped resin particle encapsulates gas in the interior thereof,
and hence has a high impact resilience. On the contrary, as the binder for the preliminary
coating layer, a rubber or a resin having a relatively low impact resilience and a
small stretch is selected. Herewith, a state can be achieved in which the preliminary
coating layer is easily polished and the hollow-shaped resin particles are hardly
polished. When the preliminary coating layer in the foregoing state is polished, the
hollow-shaped resin particles are not polished in the same state as the state of the
preliminary coating layer, but the hollow-shaped resin particles are allowed to have
the bowl shape in which the hollow-shaped resin particles are only partially scraped
away. Herewith, on the surface of the preliminary coating layer, the concave-convex
shape due to the opening of the bowl-shaped resin particles can be formed. This method
is a method in which the concave-convex shape is formed by taking advantage of the
polishability difference between the hollow-shaped resin particles and the preliminary
coating layer, and hence it is preferable to use a rubber as the binder used in the
preliminary coating layer. Among rubbers, from the viewpoint of having a low impact
resilience and a small stretch, it is particularly preferable to use acrylonitrile
butadiene rubber, styrene butadiene rubber and butadiene rubber. As the resin used
for the hollow-shaped resin particles, from the viewpoint of being low in gas permeability
and having a high impact resilience, a polar group-containing resin is preferable,
and a resin having the unit represented by the following formula (1) is more preferable.
In particular, from the viewpoint that the polishability is easily controlled, a resin
having the unit represented by formula (1) and the unit represented by formula (5)
is even more preferable.

[0069] In formula (5), R2 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.
R3 is a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. R2 and R3 may
be of the same structure or structures different from each other.
[Polishing Method]
[0070] As the polishing method, a cylinder polishing method or a tape polishing method can
be used; the polishability difference between the materials are required to be markedly
accentuated, and hence a condition of faster polishing is preferable. From this viewpoint,
it is more preferable to use the cylinder polishing method. Among the various types
of the cylinder polishing method, it is furthermore preferable to use the plunge cutting
method from the viewpoint that the positions in the lengthwise direction of the electroconductive
roller can be simultaneously polished and the polishing time can be reduced. From
the viewpoint that the polished surface is made uniform, it is preferable to make
as short as possible the time for the spark-out step (polishing step at a penetration
rate of 0 mm/min) having hitherto been performed or not to perform the spark-out step.
As an example, the number of rotations of the cylindrical grinding wheel of the plunge
cutting method is preferably 1000 to 4000 rpm, in particular, 2000 to 4000 rpm. The
penetration rate into the preliminary coating layer is preferably 5 to 30 mm/min,
and in particular, more preferably 10 to 30 mm/min. In the final stage of the penetration
step, a step of conditioning may be applied to the polishing surface, and the step
of conditioning is preferably performed at a penetration rate of 0.1 to 0.2 mm/min
for within 2 seconds. The spark-out step (polishing step at a penetration rate of
0 mm/min) is preferably performed for 3 seconds or less. The number of rotations is
preferably set at 50 rpm or more and 500 rpm or less and more preferably set at 200
rpm or more. By adopting the forgoing conditions, the concave-convex shape due to
the opening of the bowl-shaped resin particles can be more easily formed on the surface
of the preliminary coating layer, and the electroconductive roller having the electroconductive
elastic layer can be prepared.
[Electron Beam Irradiation]
[0071] The surface of the electroconductive roller thus obtained is irradiated with an electron
beam by the method described in the following (1), (2) or (3) to be subjected to curing
treatment. Herewith, the roller member of the present invention can be obtained in
which the restoring rates of elastic deformation of the middle and both ends in the
lengthwise direction have the specific relation with each other.
- (1) An electron beam irradiation method by fan-like scanning of electron beam with
the middle in the lengthwise direction of the electroconductive roller as the irradiation
center so as to extend the irradiation range toward both ends in the lengthwise direction
of the electroconductive roller.
- (2) An electron beam irradiation method by varying the acceleration voltage so as
to be larger in the middle and smaller at both ends in the lengthwise direction of
the electroconductive roller
- (3) An electron beam irradiation method with partial masking in the lengthwise direction
of the electroconductive roller by varying the acceleration voltage
[0072] The restoring rate of elastic deformation can be measured by the method in which
the restoring rate for the elastic deformation is derived from the load-displacement
curve obtained from the step of unloading after a Vickers indenter is indented to
the predetermined depth with the below-described pico-indenter. The predetermined
depth t µm is preferably 30 µm or more and 100 µm or less.
[Electron Beam Irradiation Apparatus]
[0073] A schematic view of a common electron beam irradiation apparatus is shown in FIG.
7. The electron beam irradiation apparatus used in the present invention is an apparatus
capable of irradiating with electron beam the surface of the electroconductive roller
while the electroconductive roller is being rotated, and is provided with an electron
beam generating section 71, an irradiation chamber 72 and an irradiation opening 73
as shown in FIG. 7.
[0074] The electron beam generating section 71 has an acceleration tube 75 for accelerating
the electron beam generated in an electron source (electron gun) 74 in a vacuum space
(acceleration space). The interior of the electron beam generating section is maintained
in a vacuum of 10
-3 to 10
-6Pa, with a not-shown vacuum pump or the like, in order to prevent electrons from losing
energy by the collision with gas molecules.
[0075] When a filament 76 is heated by applying an electric current to the filament 76 with
a not-shown electric power source, the filament 76 emits thermal electrons, and the
thermal electrons are effectively taken out as the electron beam. After the electron
beam is accelerated by the acceleration voltage in the acceleration space in the acceleration
tube 75, the electron beam pierces through the irradiation opening foil 77 and is
allowed to irradiate the electroconductive roller 78 being conveyed in the irradiation
chamber 72 beneath the irradiation opening 73.
[0076] In the case where the electroconductive roller 78 is irradiated with an electron
beam as it is the case in the present embodiment, the interior of the irradiation
chamber 72 is made to have a nitrogen atmosphere. The electroconductive roller 78
is rotated with a roller rotating member 79 and is moved in the irradiation chamber
by a convey unit from the left side to the right side in FIG. 7. The periphery of
the electron beam generating section 71 and the periphery of the irradiation chamber
72 are shielded with a not-shown lead or stainless steel so as for the X-ray secondarily
generated at the time of electron beam irradiation not to leak to outside.
[0077] The irradiation opening foil 77 is made of a metal foil, and serves as a partition
between the vacuum atmosphere inside the electron beam generating section and the
nitrogen atmosphere inside the irradiation chamber; the electron beam is taken out
into the inside of the irradiation chamber through the intermediary of the irradiation
opening foil 77. Accordingly, the irradiation opening foil 77 disposed in the boundary
between the electron beam generating section 71 and the irradiation chamber 72 desirably
has no pinhole, has a mechanical strength capable of sufficiently maintaining the
vacuum atmosphere inside the electron beam generating section and easily allows the
electron beam to transmit therethrough. For that purpose, the irradiation opening
foil 77 is preferably a metal foil small in specific gravity and thin in thickness;
usually, as the irradiation opening foil 77, aluminum foil, titanium foil, beryllium
foil and carbon film are used. For example, a thin film foil having a thickness of
about 5 µm or more and 30 µm or less is used. The conditions of the curing treatment
with electron beam are determined by the acceleration voltage and the dose of the
electron beam. The acceleration voltage affects the curing treatment depth, and the
condition of the acceleration voltage in the present invention is preferably such
that the acceleration voltage falls within a low energy region, a range from 40 to
300 kV. The acceleration voltage of 40 kV or more enables to obtain a treatment region
sufficiently thick for attaining the advantageous effect of the present invention.
A more preferable acceleration voltage falls within a range from 70 to 150 V.
[0078] The dose of the electron beam in the electron beam irradiation is defined by the
following calculation formula (3):

[0079] Here, D represents the dose (kGy), K represents the apparatus constant, I represents
the electronic current (mA), and V represents the processing speed (m/min). The apparatus
constant K is a constant representing the efficiency of the respective apparatus and
an index indicating the performance of the apparatus. The apparatus constant K can
be determined by measuring the does by varying the electronic current and the processing
speed under a predetermined condition of the acceleration voltage. The measurement
of the dose of the electron beam is performed by attaching a dose measurement film
on the surface of the electroconductive roller, irradiating the surface of the electroconductive
roller with the electron beam, and measuring the dose of the dose measurement film
with a film dosimeter. The dose measurement film FWT-60 and the film dosimeter model
FWT-92 (both manufactured by Far West Technology, Inc.) are used.
[0080] The dose of the electron beam in the present invention preferably falls within a
range from 30 to 3000 kGy. When the dose is 30 kGy or more, the restoring rate for
an elastic deformation sufficient for obtaining the advantageous effect of the present
invention can be obtained. The dose set to be 3000 kGy or less does not harden the
electroconductive elastic layer to an unnecessarily high hardness, and improves the
follow-up rotation performance in relation to the photosensitive member.
[Scanning Electron Beam Irradiation Source]
[0081] Next, the scanning electron beam irradiation source usable in the present invention
is described in detail. As shown in FIG. 8, the scanning electron beam irradiation
source is provided with an electron gun 81, a vessel 82 of the electron beam generating
section and an irradiation opening 83. The scanning electron beam irradiation source
is an apparatus for performing electron beam irradiation by radiating electron beam
from an irradiation opening 83 while the electron beam is being scanned in a fan-like
scanning mode by fast deflecting the electron beam emitted from the electron gun 81
to a predetermined direction.
[0082] The electron gun 81 has a filament 84 for emitting electron beam. An electromagnetic
coil 86 is disposed around the electron beam passage hole 85 along the emitting axis
of the electron beam emitted from the filament 84. The disposition center of the electromagnetic
coil 86 coincides with the central axis of the electron beam passage hole 85. The
electromagnetic coil is designed to focus the electron beam passing through the electron
beam passage hole 85 toward the irradiation opening 83. A not-shown vacuum pump is
connected to the side of the vessel 82 of the electron beam generating section, and
the interior of the electron beam generating section is maintained in a vacuum of
10
-3 to 10
-6Pa, in order to prevent electrons from losing energy by the collision with gas molecules.
[0083] The vessel 82 of the electron beam generating section is provided with a deflection
coil, the electron beam passing through the electron beam passage hole 85 is deflected
in a fan-like spread by the deflection coil 87. The deflection coil 87 is operated
based on the electric current value and the frequency supplied from a not-shown alternating
current electric power source, and consequently, the electron beam is fast deflected
from side to side as shown in FIG. 8. The frequency of the deflected electron beam
is preferably set at 100 Hz or more in order not to cause the occurrence of the electron
beam irradiation unevenness.
[0084] The electron beam deflected in a fan-like spread by the deflection coil 87 transmits
the irradiation window 88 disposed at the irradiation opening 83, and the surface
of the electroconductive roller 89 disposed outside the scanning electron beam irradiation
source is irradiated with the electron beam. The irradiation window 88 of the electron
beam is formed with, for example, a titanium foil or a beryllium foil having a thickness
of a few microns to about 10 µm.
[0085] By performing the surface treatment of the electroconductive elastic layer with the
scanning electron beam irradiation source, the electroconductive elastic layer according
the present invention can be obtained in which the restoring rates for the elastic
deformation at the surface and at the position of the depth of t µm from the surface
are reversed in the middle and at both ends in the lengthwise direction.
[0086] Specifically, as shown in FIG. 8, the electron beam irradiation is performed in a
fan-like spread with the middle in the lengthwise direction of the electroconductive
roller as the irradiation center so as to symmetrically extend the irradiation range
toward both ends of the electroconductive elastic layer of the electroconductive roller.
Herewith, the electron beam with which the middle in the lengthwise direction of the
electroconductive elastic layer is irradiated and the electron beam with which both
ends in the lengthwise direction of the electroconductive elastic layer are irradiated
are the same with respect to the acceleration voltage, but these electron beams are
different in the incident angle to the electroconductive elastic layer, and hence
are different in the extent of the permeation of the electron beam in the depth direction
of the electroconductive elastic layer. Consequently, the electron beam permeates
more deeply in the middle than at both ends in the lengthwise direction of the electroconductive
elastic layer.
[0087] Consequently, the roller member according the present invention, provided with the
following properties 1) to 3) can be obtained.
- 1) The restoring rate for the elastic deformation of the electroconductive elastic
layer is smaller from the surface toward the depth direction of the electroconductive
elastic layer.
- 2) The restoring rates in the middle and at both ends in the lengthwise direction
of the electroconductive elastic layer are such that the values at both ends are larger
than the value in the middle on the surface of the electroconductive elastic layer.
- 3) The restoring rate at the position of the depth of t µm from the surface of the
electroconductive elastic layer is such that the value in the middle is larger than
the values at both ends.
[0088] Moreover, the roller member according the present invention can also be obtained
by performing the electron beam irradiation in a fan-like spread by using the scanning
electron beam irradiation window, while the acceleration voltage is being controlled
to be higher in the middle and to be lower at both ends in the lengthwise direction
of the electroconductive roller.
[Area-Type Electron Beam Irradiation Source]
[0089] Next, the area-type electron beam irradiation source usable in the present invention
is described in detail. As shown in FIG. 9, the area-type electron beam irradiation
source is provided with an electron gun 91, a vessel 92 of the electron beam generating
section and an irradiation opening 93. The area-type electron beam irradiation source
is an apparatus in which the electron beam emitted from the electron gun 91 is accelerated
by an acceleration tube 94 in the vacuum space (acceleration space), and the electron
beam is radiated linearly from an irradiation opening 93 to irradiate a predetermined
area.
[0090] The electron gun 91 has a plurality of filaments 95 to emit electron beams. The electron
beams emitted by the plurality of filaments 95 are accelerated by an acceleration
tube 94 in the vacuum space (acceleration space), and are radiated toward an irradiation
opening 93. A not-shown vacuum pump is connected to the side of the vessel 92 of the
electron beam generating section, and the interior of the electron beam generating
section and the acceleration tube 94 are each maintained in a vacuum of 10
-3 to 10
-6 Pa, in order to prevent electrons from losing energy by the collision with gas molecules.
[0091] The linear electron beams emitted from the plurality of filaments 95 transmit through
the window 96 disposed in the irradiation opening 93, and the surface of the roller
member 97 disposed outside the area-type electron beam irradiation source is irradiated
with the electron beams. The irradiation window 96 of the electron beams is formed
with, for example, a titanium foil or a beryllium foil having a thickness of a few
microns to about 10 µm.
[0092] The use of the area-type electron beam irradiation source enables the control of
the restoring rate for the elastic deformation in the depth direction of the electroconductive
elastic layer. Specifically, as shown in FIG. 9, a masking 98 is performed on the
surface of the electroconductive roller, except for the predetermined width (for example,
10 mm) at each of both ends in the lengthwise direction of the electroconductive roller,
and the electroconductive roller is irradiated with the electron beams having a low
acceleration voltage. Subsequently, the masking 98 is performed on the surface of
the electroconductive roller while the non-masking sections are being sequentially
moved each by the predetermined width toward the middle, and the irradiation can be
achieved by performing the irradiation repeatedly in such a way that every time the
non-masking sections are moved, the acceleration voltage is gradually made higher.
[0093] By adopting such a masking operation, both ends of the electroconductive roller can
be irradiated with the electron beam having a low acceleration voltage, and the middle
of the electroconductive roller can be irradiated with the electron beam having a
high acceleration voltage. Consequently, the distances of reach of the electron beam
in the depth direction of the electroconductive elastic layer in the middle and at
both ends can be varied. The masking 98 on the surface of the electroconductive roller
prevents the transmission of the electron, and as the masking 98, for example, a stainless
steel sheet having a thickness of about 50 µm is used.
[0094] As described above, the roller member according the present invention provided with
the foregoing properties 1) to 3) can be obtained.
<Electrophotographic Apparatus>
[0095] The electrophotographic apparatus according the present invention is an electrophotographic
apparatus including the roller member for electrophotography and a photosensitive
member.
[0096] FIG. 10 shows a schematic configuration of an example of the electrophotographic
apparatus. The electrophotographic apparatus is constituted with, for example, an
electrophotographic photosensitive member, a charging device of the electrophotographic
photosensitive member, a latent image forming device performing photographic exposure,
a developing device, a transfer device, a cleaning device for transfer residual toner
on the electrophotographic photosensitive member and a fixing device.
[0097] The electrophotographic photosensitive member 102 is of a rotation drum type having
a photosensitive layer on an electroconductive substrate. The electrophotographic
photosensitive member is driven to rotate in the direction of an arrow at a predetermined
peripheral speed (process speed).
[0098] The charging device has a contact-type charging roller 101 to be contact disposed
with the electrophotographic photosensitive member 102 by being made to come into
contact with the electrophotographic photosensitive member 102 with a predetermined
pressure. The charging roller 101 is a driven rotation member which rotates following
the rotation of the electrophotographic photosensitive member 102, and charges the
electrophotographic photosensitive member to a predetermined electric potential by
applying a predetermined direct-current voltage from a charging electric power source
109 to the electrophotographic photosensitive member. As the latent image forming
device (not shown) forming an electrostatic latent image on the electrophotographic
photosensitive member 102, an exposure device such as a laser beam scanner is used.
An electrostatic latent image is formed by irradiating the uniformly charged electrophotographic
photosensitive member 102 with the photographic exposure light 107 corresponding to
image information.
[0099] The developing device has a development sleeve or a development roller 103 disposed
in the vicinity of or in contact with the electrophotographic photosensitive member
102. By using a toner electrostatically treated so as to have the same polarity as
the charge polarity of the electrophotographic photosensitive member and by performing
reverse development, the electrostatic latent image is developed to form a toner image.
The transfer device has a contact-type transfer roller 104. The toner image is transferred
from the electrophotographic photosensitive member to a transfer material such as
plain paper. The transfer material is conveyed by a paper feeding system having a
conveying member.
[0100] The cleaning device has a blade-type cleaning member 106 and a collecting vessel
108, and mechanically scrapes off and collects, after the transfer, the transfer residual
toner remaining on the electrophotographic photosensitive member 102. Here, the cleaning
device can also be omitted by adopting a simultaneous development and cleaning method
collecting the transfer residual toner with the developing device. The fixing roller
105 is constituted with a heated roller, fixes the transferred toner image on the
transfer material, and mechanically discharges the transfer material with the transferred
image thereon.
[0101] The roller member for electrophotography of the present invention can be used as
the foregoing development roller, charging roller, transfer roller or fixing roller.
<Process Cartridge>
[0102] The process cartridge according the present invention has the roller member for electrophotography
and an electrophotographic photosensitive member, and is a process cartridge constituted
so as to be demountable from the body of an electrophotographic apparatus.
[0103] FIG. 11 shows a schematic configuration of an example of the process cartridge. The
process cartridge is constituted by integrating, for example, the electrophotographic
photosensitive member 102, the charging roller 101, the development roller 103 and
the cleaning member 106, so as to be demountable from the electrophotographic apparatus.
The roller member for electrophotography of the present invention can be used as the
foregoing development roller or charging roller.
[Examples]
[0104] Hereinafter, the present invention is described in more detail with reference to
specific Production Examples and Examples. Production examples are classified as follows.
Production Examples 1 to 13 are production examples for resin particles. Production
Examples 14 to 18 are production examples for electroconductive rubber compositions
1 to 5 including resin particles. The average particle size of the resin particles
means a volume average particle size, and the measurement method thereof is described
below in detail.
[Measurement of Volume Average Particle Size of Resin Particles]
[0105] The measurement of the volume average particle size of a powder was performed by
using a laser diffraction particle size distribution analyzer (trade name: Coulter
LS-230 Particle Size Distribution Analyzer, manufactured by Coulter, Inc.). For the
measurement, an aqueous module was used, and pure water was used as the solvent. The
interior of the measurement system of the particle size distribution analyzer was
cleaned with pure water for about 5 minutes, 10 mg to 25 mg of sodium sulfite was
added as an antifoaming agent in the measurement system, and the background function
was performed. In 50 ml of pure water, 3 drops to 4 drops of a surfactant was added,
and further, 1 mg to 25 mg of a measurement sample was added. An aqueous solution
in which the sample had been suspended was subjected to a dispersion treatment with
an ultrasonic disperser for 1 minute to 3 minutes to prepare a test sample solution.
The measurement was performed in such a way that the test sample solution was slowly
added in the measurement system of the measurement apparatus, and the test sample
concentration in the measurement system was regulated so as for the PIDS on the screen
of the apparatus to be 45% or more and 55% or less. From the obtained volume distribution,
the volume average particle size was derived.
<Production Example 1> [Preparation of Resin Particles 1]
[0106] An aqueous mixed liquid composed of 4000 parts by mass of ion-exchange water, 9 parts
by mass of colloidal silica as a dispersion stabilizer and 0.15 part by mass of polyvinylpyrrolidone
was prepared. Next, an oily mixed liquid was prepared which was composed of 50 parts
by mass of acrylonitrile, 45 parts by mass of methacrylonitrile and 5 parts by mass
of methyl methacrylate as polymerizable monomers, 12.5 parts by mass of normal hexane
as an encapsulated substance, and 0.75 part by mass of dicumyl peroxide as a polymerization
initiator. The oily mixed liquid was added to the aqueous mixed liquid, and additionally,
0.4 part by mass of sodium hydroxide was added to prepare a dispersion.
[0107] The obtained dispersion was stirred and mixed with a homogenizer for 3 minutes, and
then the dispersion was placed in a polymerization reaction vessel the air in which
had been replaced with nitrogen and allowed to react at 60°C for 20 hours under stirring
at 200 rpm to prepare a reaction product. The obtained reaction product was repeatedly
filtered and washed with water, and then dried at 80°C for 5 hours to prepare resin
particles. The obtained resin particles were disintegrated and classified with a sonic
classifier to yield the resin particles 1 having an average particle size of 12 µm.
<Production Examples 2 to 13> [Preparation of Resin Particles 2 to 13]
[0108] The resin particles were prepared in the same manner as in Production Example 1 except
that at least one of the added amount in parts by mass of the colloidal silica, and
the type and the added parts by mass of the polymerizable monomer was altered according
to the conditions shown in Table 1. The prepared resin particles were classified in
the same manner as in Production Example 1 to yield the resin particles 2 to 13 each
having the average particle size shown in able 1.
Table 1
Production Example |
Particles No. |
Amount used of colloidal silica (parts by mass) |
Polymerizable monomer and amount used thereof (parts by mass) |
Average particle size [µm] |
1 |
Resin Particles 1 |
9 |
Acrylonitrile 50-methacrylonitrile 45-methyl acrylate 5 |
12 |
2 |
Resin Particles 2 |
4.5 |
Acrylonitrile 50-methacrylonitrile 45-methyl acrylate 5 |
50 |
3 |
Resin Particles 3 |
9 |
Acrylonitrile 80-metharylonitrile 20 |
10 |
4 |
Resin Particles 4 |
4.5 |
Acrylonitrile 80-metharylonitrile 20 |
30 |
5 |
Resin Particles 5 |
9 |
Methacrylonitrile 45-methyl acrylate 55 |
15 |
6 |
Resin Particles 6 |
4.5 |
Methacrylonitrile 45-methyl acrylate 55 |
40 |
7 |
Resin Particles 7 |
9 |
Acrylamide 45-methacrylamide 55 |
15 |
8 |
Resin Particles 8 |
4.5 |
Acrylamide 45-methacrylamide 55 |
40 |
9 |
Resin Particles 9 |
9 |
Acrylamide 100 |
8 |
10 |
Resin Particles 10 |
9 |
Methacrylamide 100 |
15 |
11 |
Resin Particles 11 |
9 |
Methyl methacrylate 100 |
10 |
12 |
Resin Particles 12 |
9 |
Acrylonitrile 100 |
15 |
13 |
Resin Particles 13 |
9 |
Vinylidene chloride 100 |
15 |
<Production Example 14> [Preparation of Electroconductive Rubber Composition 1]
[0109] To 100 parts by mass of acrylonitrile butadiene rubber (NBR) (trade name: N230SV,
manufactured by JSR Corp.), other four components shown under the heading of the component
(1) in Table 2 presented below were added, and the resulting mixture was kneaded with
a mixer regulated at 50°C for 15 minutes. Next, the three components shown under the
heading of the component (2) in Table 2 were added to the kneaded mixture, and the
mixture was kneaded with a two-roll mill cooled to a temperature of 25°C for 10 minutes,
to yield the electroconductive rubber composition 1.
Table 2
|
Materials |
Amount used (parts by mass) |
Component (1) |
Acrylonitrile butadiene rubber (NBR) (trade name: N230SV, manufactured by JSR Corp.) |
100 |
Carbon black (trade name: Tokablack #7360SB, manufactured by Tokai Carbon Co., Ltd.) |
48 |
Zinc oxide (trade name: Zinc white type 2, manufactured by Sakai Chemical Industry
Co., Ltd.) |
5 |
Zinc stearate (trade name: SZ-2000, manufactured by Sakai Chemical Industry Co., Ltd.) |
1 |
Calcium carbonate (trade name: Nanox #30, manufactured by Maruo Karushiumu Kabushiki
Gaisha) |
20 |
Component (2) |
Resin Particles 1 |
12 |
Sulfur (vulcanizing agent) |
1.2 |
Tetrabenzylthiuram disulfide (TBzTD) (trade name: Perkacit TBzTD, manufactured by
Flexis S.A.)(vulcanization promoter) |
4.5 |
<Production Example 15> [Preparation of Electroconductive Rubber Composition 2]
[0110] To 100 parts by mass of a styrene butadiene rubber (SBR) (trade name: Tufdene 2003,
manufactured by Asahi Kasei Corp.), the other six components shown under the heading
of the component (1) in Table 3 presented below were added, and the resulting mixture
was kneaded with a sealed type mixer regulated at 80°C for 15 minutes. Next, the four
components shown under the heading of the component (2) in Table 3 were added to the
kneaded mixture, and the mixture was kneaded with a two-roll mill cooled to a temperature
of 25°C for 10 minutes, to yield the electroconductive rubber composition 2.
Table 3
|
Materials |
Amount used (parts by mass) |
Component (1) |
Styrene butadiene rubber (SBR) (trade name: Tufdene 2003, manufactured by Asahi Kasei
Corp.) |
100 |
Zinc oxide (trade name: Zinc white type 2, manufactured by Sakai Chemical Industry
Co., Ltd.) |
5 |
Zinc stearate (trade name: SZ-2000, manufactured by Sakai Chemical Industry Co., Ltd.) |
1 |
Carbon black (trade name: Ketjen black EC600JD, manufactured by Lion Corp.) |
8 |
Carbon black (trade name: Seast 5, manufactured by Tokai Carbon Co., Ltd.) |
40 |
Calcium carbonate (trade name: Nanox #30, manufactured by Maruo Karushiumu Kabushiki
Gaisha) |
15 |
Paraffin oil (trade name: PW380, manufactured by Idemitsu Kosan Co., Ltd.) |
20 |
Component (2) |
Resin Particles 1 |
12 |
Sulfur (vulcanizing agent) |
1.2 |
Dibenzothiazyl disulfide (DM) (trade name: Nocceler DM, manufactured by Ouchi Shinko
Chemical Industrial Co., Ltd., vulcanization promoter) |
1 |
Tetramethylthiuram monosulfide (TS) (trade name: Nocceler TS, manufactured by Ouchi
Shinko Chemical Industrial Co., Ltd., vulcanization promoter) |
1 |
<Production Example 16> [Preparation of Electroconductive Rubber Composition 3]
[0111] The electroconductive rubber composition 3 was obtained in the same manner as in
Production Example 14 except that acrylonitrile butadiene rubber in Production Example
14 was replaced with butadiene rubber(BR) (trade name: JSR BR01, manufactured by JSR
Corp.) and the amount of carbon black was altered to 30 parts by mass.
<Production Example 17> [Preparation of Electroconductive Rubber Composition 4]
[0112] To 100 parts by mass of ethylene propylene diene copolymer (EPDM) (trade name: EP33,
manufactured by JSR Corp.), the other four components shown under the heading of the
component (1) in Table 4 presented below were added, and the resulting mixture was
kneaded with a sealed type mixer regulated at 80°C for 15 minutes. Next, the four
components shown under the heading of the component (2) in Table 4 were added to the
kneaded mixture, and the mixture was kneaded with a two-roll mill cooled to a temperature
of 25°C for 10 minutes, to yield the electroconductive rubber composition 4.
Table 4
|
Materials |
Amount used (parts by mass) |
Component (1) |
Ethylene-propylene-diene copolymer (EPDM) (trade name: EP33, manufactured by JSR Corp.) |
100 |
Carbon black (trade name: Tokablack #7360SB, manufactured by Tokai Carbon Co., Ltd.) |
40 |
Zinc oxide (trade name: Zinc white type 2, manufactured by Sakai Chemical Industry
Co., Ltd.) |
5 |
Zinc stearate (trade name: SZ-2000, manufactured by Sakai Chemical Industry Co., Ltd.) |
1 |
Calcium carbonate (trade name: Nanox #30, manufactured by Maruo Karushiumu Kabushiki
Gaisha) |
20 |
Component (2) |
Resin Particles 1 |
12 |
Sulfur (vulcanizing agent) |
1 |
Dibenzothiazyl disulfide (DM) (trade name: Nocceler DM, manufactured by Ouchi Shinko
Chemical Industrial Co., Ltd., vulcanization promoter) |
1 |
Tetramethylthiuram monosulfide (TS) (trade name: Nocceler TS, manufactured by Ouchi
Shinko Chemical Industrial Co., Ltd., vulcanization promoter) |
1 |
<Production Example 18> [Preparation of Electroconductive Rubber Composition 5]
[0113] To 100 parts by mass of epichlorohydrin rubber (EO-EP-AGE terpolymer compound, EO/EP/AGE=73
mol%/23 mol%/4 mol%), the other seven components shown under the heading of the component
(1) in Table 5 presented below were added, and the resulting mixture was kneaded with
a sealed type mixer regulated at 80°C for 15 minutes. Next, the four components shown
under the heading of the component (2) in Table 5 were added to the kneaded mixture,
and the mixture was kneaded with a two-roll mill cooled to a temperature of 25°C for
10 minutes, to yield the electroconductive rubber composition 5.
Table 5
|
Materials |
Amount used (parts by mass) |
Component (1) |
Epichlorohydrin rubber (EO-EP-AGE terpolymer compound, EO/EP/AGE=73 mol%/23 mol%/4
mol%) |
100 |
Carbon black (trade name: Thermax Flow Form N990, manufactured by Cancarb Ltd.) |
2 |
Zinc oxide (trade name: Zinc white type 2, manufactured by Sakai Chemical Industry
Co., Ltd.) |
5 |
Zinc stearate (trade name: SZ-2000, manufactured by Sakai Chemical Industry Co., Ltd.) |
1 |
Calcium carbonate (trade name: Nanox #30, manufactured by Maruo Karushiumu Kabushiki
Gaisha) |
20 |
Adipic acid ester (trade name: (Polycizer W305ELS, manufactured by Dainippon Ink and
Chemicals, Inc.) |
8 |
Quaternary ammonium salt (trade name: Adeka Sizer LV70, manufactured by Asahi Denka
Kogyo Co., Ltd.) |
2 |
2-Mercaptobenzimidazole (anti-aging agent) |
0.5 |
Component (2) |
Resin Particles 1 |
12 |
Sulfur (vulcanizing agent) |
1 |
Dibenzothiazyl disulfide (DM) (trade name: Nocceler DM, manufactured by Ouchi Shinko
Chemical Industrial Co., Ltd., vulcanization promoter) |
1 |
Tetramethylthiuram monosulfide (TS) (trade name: Nocceler TS, manufactured by Ouchi
Shinko Chemical Industrial Co., Ltd., vulcanization promoter) |
1 |
<Example 1>
[0114] As shown in FIG. 3A, Example 1 relates to a roller member having an electroconductive
elastic layer on an electroconductive substrate.
[1. Electroconductive Substrate]
[0115] A thermosetting resin containing 10% by mass of carbon black is applied on a stainless
steel substrate of 6 mm in diameter and 252.5 mm in length and dried; the thus treated
substrate was used as an electroconductive substrate.
[2. Formation of Electroconductive Elastic Layer]
[0116] By using an extrusion molding apparatus equipped with a cross head die, the outer
peripheral surface of the conductive substrate was coated with the electroconductive
rubber composition 1 prepared in Production Example 14, in a cylindrical shape with
the electroconductive substrate serving as a central axis. The coating thickness of
the electroconductive rubber composition was regulated to be 1.75 mm.
[0117] The roller after treating with the extrusion molding apparatus was heated in a hot
air furnace at 160°C for 1 hour to vulcanize the electroconductive rubber composition,
and then the ends of the rubber layer was removed to regulate the length of the rubber
layer to be 224.2 mm. Additionally, a secondary vulcanization was performed at 160°C
for 1 hour, to prepare a roller having a preliminary coating layer of 3.5 mm in layer
thickness. The obtained outer peripheral surface of the roller was polished with a
plunge cutting type cylinder polishing machine. As the polishing abrasive grain, a
vitrified grinding stone was used, and the abrasive grain is made of a green silicon
carbide (GC) and the particle size was set at 100 mesh. The number of rotations of
the roller was set at 350 rpm, and the number of rotations of the grinding wheel was
set at 2050 rpm. The cutting speed was set at 20 mm/min, the spark-out time (the time
at cutting of 0 mm) was set at 0 second, and the polishing was performed to prepare
an electroconductive roller having an electroconductive elastic layer. The thickness
of the electroconductive elastic layer was regulated to be 1.5 mm. The crown quantity
of the resulting roller was found to be 120 µm.
[3. Irradiation of Electroconductive Elastic Layer with Electron Beam]
[0118] The electroconductive roller was irradiated with electron beam under the following
conditions to yield the roller member 1. The electron beam irradiation was performed
with an electron beam irradiation apparatus (trade name: low energy electron beam
irradiation source EB-ENGINE, manufactured by Hamamatsu Photonics K.K.). The irradiation
with electron beam was performed in such a way that the oxygen concentration of the
atmosphere was regulated to be 500 ppm or less by nitrogen gas purge, and while the
roller member was being rotated at 300 rpm with the electroconductive substrate of
the roller member as a rotation axis, the roller member was conveyed at a processing
speed of 10 mm/s in the direction perpendicular to the plane of FIG. 8. The electron
beam irradiation conditions were such that the acceleration voltage was 70 kV, and
the electronic current was regulated so as for the dose to be 1000 kGy.
[4. Evaluation of Roller Member]
[0119] In the roller member 1 thus obtained were evaluated with respect to the following
[4-1] to [4-6]. The evaluation results thus obtained are shown in Table 11 and Table
13.
[4-1. Measurements of Surface Roughness Rzjis and Mean Concave-Convex Spacing Sm of
Roller Member]
[0120] The surface roughness and the mean concave-convex spacing are measured according
to the surface roughness standards of JIS B 0601-1994 by using a surface roughness
tester (trade name: SE-3500, manufactured by Kosaka Laboratory Ltd.). The surface
roughness values and the concave-convex spacings are measured at randomly selected
six positions on the surface of the roller member, and the average values of the surface
roughness and the concave-convex spacing are adopted as Rzjis and Sm. It is to be
noted that the cut-off value is 0.8 mm and the evaluation length is 8 mm.
[4-2. Shape Measurement of Bowl-Shaped Resin Particles]
[0121] The arbitrary points on the electroconductive elastic layer are cut every 20 nm over
500 µm with a focused ion beam (trade name: FB-2000C, manufactured by Hitachi, Ltd.),
the cross sectional images at these points are photographed. By combining the photographed
images of one and the same bowl-shaped resin particle, the three-dimensional image
of the bowl-shaped resin particle is derived. From the three-dimensional image, "the
maximum diameter" 55 is derived as shown in FIG. 6A to FIG. 6E, and "the minimum diameter
of the opening" 63 shown in FIG. 6A to FIG. 6E are derived. From the three-dimensional
image, at arbitrary five points on the bowl-shaped resin particles, "the difference
between the outer diameter and the inner diameter" (namely, "the thickness of the
shell") is derived. Such operations as described above are performed for the 10 resin
particles within the field of view. The same measurement is performed at 10 positions
in the lengthwise direction of the roller member, and the average value is derived
for the values derived for the 100 resin particles thus obtained in total.
[4-3. Measurement of Surface Profile of Roller Member]
[0122] The surface of the roller member is observed with a laser microscope (trade name:
LXM5 PASCAL, manufactured by Carl Zeiss Ltd.) in a field of view of 0.5 mm in length
and 0.5 mm in width. By scanning the laser on the X-Y plane within the field of view,
a two-dimensional image data is obtained, and then the focal point is moved in the
Z direction and the foregoing scanning is repeated; in this way a three-dimensional
image data is obtained. Consequently, first, it is verified that the bowl-shaped resin
particles have the concavities derived from the openings and the protrusions derived
from the edges. Additionally, "the height difference" 54 between the top of the protrusion
53 and the bottom of the concavity 52 is derived. Such an operation is performed for
the two bowl-shaped resin particles within the field of view. The same measurement
is performed at 50 positions in the lengthwise direction of the roller member, and
the average value of the measured values of the 100 resin particles obtained in total
is derived.
[4-4. Measurement of Restoring Rate for Elastic Deformation of Roller Member]
[0123] Based on ISO 14577, the restoring rate was measured with the Picodentor HM500 (trade
name, manufactured by Fischer Instruments KK). As the indenter, an indenter (Vickers
pyramid) was used which is a pyramid-type diamond indenter having a square base and
angle of 136° between the opposite faces at the vertex. The measurement was performed
in the middle and at both ends (each 90 mm from the middle toward the end) in the
lengthwise direction.
[0124] The measurement includes a step (hereinafter, referred to as an "indentation step")
of indenting the indenter at a predetermined speed to a predetermined depth, and a
step (hereinafter, referred to as a "unloading step") of unloading the load from the
position of the predetermined indentation depth at a predetermined speed. From the
load-displacement curve thus obtained as shown in FIG. 12, the restoring rate for
the elastic deformation was derived. The method for deriving the restoring rate is
described below.
[0125] The measurement was performed under the following two conditions, and in the case
where there was a region where the bowl-shaped resin particles were absent, a non-resin
particle portion was selected. It is to be noted that FIG. 12 shows an example of
the load-displacement curve in the case of t = 100 µm in the <condition 2>.
<Condition 1> Measurement of Restoring Rate on Surface
[0126]
(Indentation Step)
- Maximum indentation depth = 10 µm
- Indentation time = 20 seconds
It is to be noted that the maximum load F
max was required to be sufficiently large so as to enable the indentation to the maximum
indentation depth, and thus set at 10 mN in the present measurement.
(Unloading Step)
- Minimum load = 0.005 mN
- Unloading time = 1 second
It is to be noted that the unloading was performed until the minimum load of the indenter
was reached.
[0127] The restoring rate v for the elastic deformation was derived from the displacement
(=the restored distance L of the electroconductive elastic layer) of the indenter
at 0.1 second form the start of the unloading in the unloading step, with the following
formula:

<Condition 2> Measurement of Restoring Rate at Predetermined Depth t µm
[0128]
(Indentation Step)
- Maximum indentation depth (predetermined depth t) = 20, 30, 50, 100 µm
- Indentation time = 20 seconds
It is to be noted that the maximum load was required to be a sufficiently large value
so as to enable the indentation to the maximum indentation depth, and thus set at
300 mN in the present measurement.
(Unloading Step)
- Minimum load = 0.005 mN
- Unloading time = (maximum indentation depth)/10 sec
[0129] The unloading was performed until the minimum load of the indenter was reached. The
unloading time is determined by the maximum indentation depth in the indentation step;
for example, in the case of the maximum indentation depth t = 20 µm, the unloading
time is 2 seconds. This is for the purpose of equalizing the unloading rates of the
condition 1 and the condition 2. The derivation of the restoring rate v for the elastic
deformation was performed in the same manner as in the case of the condition 1.
[4-5. Image Evaluation 1] Evaluation of Abrasion Property
[0130] The monochromatic laser printer ("LaserJet P4515n" (trade name), manufactured by
Hewlett-Packard Japan, Ltd.), which is an electrophotographic apparatus having the
configuration shown in FIG. 10, was used and a voltage was applied to the charging
roller from the outside. The applied voltage was an alternating-current voltage, and
the peak-to-peak voltage (Vpp) was set at 1800 V, the frequency (f) was set at 2930
Hz, and the direct-current voltage (Vdc) was set at -600 V. The output image resolution
was 600 dpi. As the process cartridge, a process cartridge for the foregoing printer
was used. The attached charging roller was dismounted from process cartridge, and
the roller member 1 was set as the charging roller. The roller member 1 was made to
come into contact with the electrophotographic photosensitive member with a pushing
pressure of 4.9 N due to a spring at one end and a total pushing pressure of 9.8 N
due to springs at both ends. The roller member 1 was set in the process cartridge,
and the process cartridge was preconditioned in a high-temperature and high-humidity
environment of a temperature of 32.5°C and a relative humidity of 80% for 24 hours.
[0131] Next, the following image evaluation was performed. First, a two-sheet intermittent
print endurance test (an endurance test in which the rotation of the printer was stopped
every two output sheets for 3 seconds) was performed in which a horizontal-line image
of two dots in width and 176 dots in spacing was output in the direction perpendicular
to the rotational direction of the electrophotographic photosensitive member. After
the output of 20000 printed sheets, a halftone image (in the direction perpendicular
to the rotational direction of the electrophotographic photosensitive member, an image
depicting a horizontal line of one dot in width and two dots in spacing) was output
and evaluated. In the evaluation, the halftone image was visually observed and whether
or not a dot-like, a horizontal line-like, or a vertical line-like image defect due
to the uneven abrasion of the photosensitive member was found was evaluated based
on the following standards.
Table 6
Rank |
Evaluation standard |
1 |
No dot-like, holizontal line-like and vertical line-like image defects are found. |
2 |
Dot-like, holizontal line-like and vertical line-like image defects are slightly found. |
3 |
Dot-like and holizontal line-like defects are found to occur in a manner corresponding
to the rotation pitch of the roller member. Vertical line-like image defects are also
partially found. |
4 |
Dot-like, holizontal line-like and vertical line-like image defects are conspicuous. |
[4-6. Image Evaluation 2] Evaluation of Occurrence State of Banding
[0132] The process cartridge was preconditioned in a low-temperature and low-humidity environment
of a temperature of 15°C and a relative humidity of 10% for 24 hours, and then an
evaluation was performed with the same electrophotographic apparatus and under the
same voltage application condition as in the evaluation of the abrasion property in
the image evaluation 1.
[0133] After the output of 20000 printed sheets, a halftone image (in the direction perpendicular
to the rotational direction of the electrophotographic photosensitive member, an image
depicting a horizontal line of one dot in width and two dots in spacing) was output.
Then, the resulting halftone image was visually observed and whether or not the banding,
namely, a horizontal line-like density unevenness due to the uneven charging was found
was evaluated based on the following standards.
Table 7
Rank |
Evaluation standard |
1 |
No banding occurs. |
2 |
Only slight banding is found. |
3 |
Banding is partially found with the rotation pitch of the roller member, but causes
no problem in practical use. |
4 |
Banding is conspicuous, and the image quality degradation is found. |
<Examples 2 to 10, 13 to 32, 34 to 40, 42 to 48, and 50 to 56>
[0134] At least one of the following items was altered to the condition shown in Table 9:
the type and the added number of parts of the resin particles, the type of the electroconductive
rubber composition, the cutting speed at the time of polishing, the crown quantity
of the electroconductive elastic layer, the electron beam dose in the electron beam
irradiation, and the electron acceleration voltage in the electron beam irradiation.
Otherwise, in the same manner as in Example 1, roller members 2 to 10, 13 to 32, 34
to 40, 42 to 48, and 50 to 56 were prepared.
<Example 11>
[0135] A roller member 11 was prepared in the same manner as in Example 1 except that the
method of the electron beam irradiation was altered to the following method.
[0136] In performing the electron beam irradiation, the surface of the electroconductive
elastic layer was coated by placing a 100-µm thick stainless steel sheet on the central
part exclusive of both ends each having a width of 15 mm, of the length of 224.2 mm
in the lengthwise direction of the electroconductive elastic layer of the electroconductive
roller. In this state, the surface of the electroconductive elastic layer was irradiated
with an electron beam having an acceleration voltage of 80 kV, by using an area-type
electron beam irradiation source (trade name: EC150/45/40 mA, manufactured by Iwasaki
Electric Co., Ltd.), and thus both ends each having a width of 15 mm of the electroconductive
elastic layer were surface-treated.
[0137] Next, each of the areas of the electroconductive elastic layer exclusive of the areas
each extending from 15 mm to 30 mm from the end concerned in the lengthwise direction
of the electroconductive elastic layer was coated with a stainless steel sheet, and
the areas each extending from 15 mm to 30 mm from the end concerned in the lengthwise
direction of the electroconductive elastic layer were irradiated with an electron
beam having an acceleration voltage of 90 kV.
[0138] Next, each of the areas of the electroconductive elastic layer exclusive of the areas
each extending from 30 mm to 45 mm from the end concerned in the lengthwise direction
of the electroconductive elastic layer was coated with a stainless steel sheet, and
the areas each extending from 30 mm to 45 mm from the end concerned in the lengthwise
direction of the electroconductive elastic layer were irradiated with an electron
beam having an acceleration voltage of 100 kV.
[0139] Next, each of the areas of the electroconductive elastic layer exclusive of the areas
each extending from 45 mm to 60 mm from the end concerned in the lengthwise direction
of the electroconductive elastic layer was coated with a stainless steel sheet, and
the areas each extending from 45 mm to 60 mm from the end concerned in the lengthwise
direction of the electroconductive elastic layer were irradiated with an electron
beam having an acceleration voltage of 110 kV.
[0140] Next, each of the areas of the electroconductive elastic layer exclusive of the areas
each extending from 60 mm to 75 mm from the end concerned in the lengthwise direction
of the electroconductive elastic layer was coated with a stainless steel sheet, and
the areas each extending from 60 mm to 75 mm from the end concerned in the lengthwise
direction of the electroconductive elastic layer were irradiated with an electron
beam having an acceleration voltage of 120 kV.
[0141] Next, each of the areas of the electroconductive elastic layer exclusive of the areas
each extending from 75 mm to 90 mm from the end concerned in the lengthwise direction
of the electroconductive elastic layer was coated with a stainless steel sheet, and
the areas each extending from 75 mm to 90 mm from the end concerned in the lengthwise
direction of the electroconductive elastic layer were irradiated with an electron
beam having an acceleration voltage of 130 kV.
[0142] Next, each of the areas of the electroconductive elastic layer exclusive of the areas
each extending from 90 mm to 105 mm from the end concerned in the lengthwise direction
of the electroconductive elastic layer was coated with a stainless steel sheet, and
the areas each extending from 90 mm to 105 mm from the end concerned in the lengthwise
direction of the electroconductive elastic layer were irradiated with an electron
beam having an acceleration voltage of 140 kV.
[0143] Finally, each of the areas of the electroconductive elastic layer exclusive of the
areas each extending over a width of 7.1 mm from the center toward the end concerned
in the lengthwise direction of the electroconductive elastic layer (namely, the central
area having a total width of 14.2 mm) was coated with a stainless steel sheet, and
the area having the width of 14.2 mm was irradiated with an electron beam having an
acceleration voltage of 150 kV.
[0144] By applying a nitrogen gas purge to the atmosphere at the time of irradiation, the
oxygen concentration of the atmosphere was regulated to be 500 ppm or less, and while
the electroconductive roller was being rotated at 500 rpm, the electroconductive roller
was conveyed in the direction perpendicular to the plane of FIG. 9 at a processing
speed of 10 mm/sec. The electron beam irradiation conditions were such that the electronic
current was regulated so as for the dose at each of the acceleration voltages to be
1000 kGy.
<Example 12>
[0145] A roller member 12 was prepared in the same manner as in Example 11 except that the
resin particles 1 were replaced with the resin particles 2.
<Examples 33, 41, 49 and 57>
[0146] Roller members 33, 41, 49 and 57 were prepared in the same manner as in Example 1
except that the electroconductive rubber composition 1 was replaced with the electroconductive
rubber compositions shown in Table 9, respectively.
[0147] Table 9 collects, for the roller members No. 1 to 57 according to Examples 1 to 57,
the sequential numbers of the electroconductive rubber compositions and the sequential
numbers and the parts by mass of the resin particles, the polishing conditions, the
crown quantities and the electron beam irradiation conditions used for the production
of these roller members. Tables 11 and 13 show the evaluation results of the roller
members according to individual Examples.
<Comparative Example 1>
[0148] A roller member 58 was prepared in the same manner as in Example 1 except that no
electron beam irradiation was performed.
<Comparative Example 2>
[0149] A roller member 59 was prepared in the same manner as in Example 1 except that the
electron beam irradiation method was altered to the following method. The electron
beam irradiation was performed with an area-type electron beam irradiation source
(trade name: EC150/45/40 mA, manufactured by Iwasaki Electric Co., Ltd.). The irradiation
with electron beam was performed in such a way that the oxygen concentration of the
atmosphere was regulated to be 500 ppm or less by nitrogen gas purge, and while the
electroconductive roller member was being rotated at 500 rpm with the electroconductive
substrate as a rotation axis, the roller member was conveyed at 10 mm/sec. The electron
beam irradiation conditions were such that the acceleration voltage was 80 kV, and
the electronic current was regulated so as for the dose to be 1000 kGy.
<Comparative Example 3>
[0150] A roller member 60 was prepared in the same manner as in Comparative Example 2 except
that the electron acceleration voltage in the electron beam irradiation was altered
from 80 kV to 150 kV.
<Comparative Example 4>
[0151] A roller member 61 was prepared in the same manner as in Example 50 except that an
electroconductive elastic layer was prepared by adding no resin particles and by performing
no electron beam irradiation, and then an electroconductive surface layer was prepared
by the following method.
[Method for Forming Electroconductive Surface Layer]
[0152] To a caprolactone-modified acrylic polyol solution "Placcel DC2016" (trade name,
manufactured by Daicel Chemical Industries, Ltd.), methyl isobutyl ketone was added
so as to regulate the solid content of the resulting solution to be 10% by mass. To
1000 parts by mass (acrylic polyol solid content: 100 parts by mass) of the solution,
other three components shown in Table 8 were added to prepare a mixed solution.
Table 8
Materials |
Amount used (parts by mass) |
Caprolactone-modified acrylic polyol solution "Placcel DC2016" (trade name, manufactured
by Daicel Chemical Industries, Ltd.) |
100 |
Carbon black (trade name: MA-100, manufactured by Mitsubishi Carbon Co., Ltd.) |
45 |
Modified dimethyl silicone oil (trade name: SH28PA, manufactured by Dow Corning Toray
Silicone Co., Ltd.) |
0.08 |
Blocked isocyanate mixture (5:5 mixture of hexamethylene diisocyanate (HDI) and isophorone
diisocyanate (IPDI) each blocked with butanone oxime) |
25 |
[0153] Next, in a glass bottle having an internal volume of 450 mL, 200 parts by mass of
the foregoing mixed solution was placed together with 200 parts by mass of glass beads
having an average particle size of 0.8 mm, and the mixed solution was dispersed with
a paint shaker disperser for 24 hours. Subsequently, polymethyl methacrylate resin
particles (average particle size: 20 µm) were added to the mixed solution, the resulting
mixture was again dispersed for 5 minutes, and the glass beads were removed to prepare
an electroconductive resin coating liquid.
[0154] An electroconductive roller having an electroconductive elastic layer having been
subjected to polishing was immersed in the electroconductive resin coating liquid
with the lengthwise direction of the electroconductive roller oriented vertically,
and thus the electroconductive roller was coated by a dipping method. The coating
conditions were such that the immersion time was set at 9 seconds, and the pulling
speed from the electroconductive resin coating liquid was such that the initial speed
was set at 20 mm/sec, the final speed was set at 2 mm/sec, and the speed was linearly
varied as a function of time between the start and the termination. The resulting
coated product was air-dried at normal temperature for 30 minutes, then dried in a
hot-air circulation dryer at a temperature of 80°C for 1 hour, and further dried at
a temperature of 160°C for 1 hour. In this way, the roller member 61 was prepared
in which the surface layer was formed on the outer peripheral surface of the electroconductive
elastic layer.
<Comparative Example 5>
[0155] A roller member 62 was prepared in the same manner as in Example 1 except that no
resin particles were added, and 15 parts by mass of ADCA (azodicarbonamide) was added
as a foaming agent.
[0156] Table 10 collects, for the roller members No. 58 to 62 according to Comparative Examples
1 to 5, the sequential numbers of the electroconductive rubber compositions and the
sequential numbers and the parts by mass of the resin particles, the polishing conditions,
the crown quantities and the electron beam irradiation conditions used for the production
of these roller members. Tables 12 and 14 show the evaluation results of the roller
members according to individual Comparative Examples.
Table 9
Example |
Roller member No. |
Electroconductive rubber composition No. |
Resin Particles |
Polishing conditions |
Crown quantity [µm] |
Electron beam irradiation conditions |
Particle No. |
Number of parts [phr] |
Cutting speed [mm/min] |
Irradiation Source |
Acceleration voltage [kV] |
Electron beam dose [kGy] |
1 |
1 |
1 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
2 |
2 |
1 |
1 |
18 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
3 |
3 |
1 |
2 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
4 |
4 |
1 |
2 |
18 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
5 |
5 |
1 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
500 |
6 |
6 |
1 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
2000 |
7 |
7 |
1 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
60 |
1000 |
8 |
8 |
1 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
50 |
1000 |
9 |
9 |
1 |
1 |
12 |
20 |
30 |
Scanning type (FIG. 8) |
70 |
1000 |
10 |
10 |
1 |
1 |
12 |
20 |
200 |
Scanning type (FIG. 8) |
70 |
1000 |
11 |
11 |
1 |
1 |
12 |
20 |
120 |
Area type (FIG. 9) |
80-150 |
1000 |
12 |
12 |
1 |
2 |
12 |
20 |
120 |
Area type (FIG. 9) |
80-150 |
1000 |
13 |
13 |
1 |
3 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
14 |
14 |
1 |
4 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
15 |
15 |
1 |
5 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
16 |
16 |
1 |
6 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
17 |
17 |
1 |
7 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
18 |
18 |
1 |
8 |
12 |
20 |
120 |
Scanning tvpe (FIG. 8) |
70 |
1000 |
19 |
19 |
1 |
9 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
20 |
20 |
1 |
10 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
21 |
21 |
1 |
11 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
22 |
22 |
1 |
12 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
23 |
23 |
1 |
13 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
24 |
24 |
1 |
4 |
12 |
10 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
25 |
25 |
1 |
4 |
12 |
30 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
26 |
26 |
2 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
27 |
27 |
2 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
500 |
28 |
28 |
2 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
2000 |
29 |
29 |
2 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
60 |
1000 |
30 |
30 |
2 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
50 |
1000 |
31 |
31 |
2 |
1 |
12 |
20 |
30 |
Scanning type (FIG. 8) |
70 |
1000 |
32 |
32 |
2 |
1 |
12 |
20 |
200 |
Scanning type (FIG. 8) |
70 |
1000 |
33 |
33 |
2 |
1 |
12 |
20 |
120 |
Area type (FIG. 9) |
80-150 |
1000 |
34 |
34 |
3 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
35 |
35 |
3 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
500 |
36 |
36 |
3 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
2000 |
37 |
37 |
3 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
60 |
1000 |
38 |
38 |
3 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
50 |
1000 |
39 |
39 |
3 |
1 |
12 |
20 |
30 |
Scanning type (FIG. 8) |
70 |
1000 |
40 |
40 |
3 |
1 |
12 |
20 |
200 |
Scanning type (FIG. 8) |
70 |
1000 |
41 |
41 |
3 |
1 |
12 |
20 |
120 |
Area type (FIG. 9) |
80-150 |
1000 |
42 |
42 |
4 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
43 |
43 |
4 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
500 |
44 |
44 |
4 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
2000 |
45 |
45 |
4 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
60 |
1000 |
46 |
46 |
4 |
I |
12 |
20 |
120 |
Scanning type (FIG. 8) |
50 |
1000 |
47 |
47 |
4 |
1 |
12 |
20 |
30 |
Scanning type (FIG. 8) |
70 |
1000 |
48 |
48 |
4 |
1 |
12 |
20 |
200 |
Scanning type (FIG. 8) |
70 |
1000 |
49 |
49 |
4 |
1 |
12 |
20 |
120 |
Area type (FIG. 9) |
80-150 |
1000 |
50 |
50 |
5 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
51 |
51 |
5 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
500 |
52 |
52 |
5 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
70 |
2000 |
53 |
53 |
5 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
60 |
1000 |
54 |
54 |
5 |
1 |
12 |
20 |
120 |
Scanning type (FIG. 8) |
50 |
1000 |
55 |
55 |
5 |
1 |
12 |
20 |
30 |
Scanning type (FIG. 8) |
70 |
1000 |
56 |
56 |
5 |
1 |
12 |
20 |
200 |
Scanning type (FIG. 8) |
70 |
1000 |
57 |
57 |
5 |
1 |
12 |
20 |
120 |
Area type (FIG. 9) |
80-150 |
1000 |
Table 10
Comparative Example |
Roller member No. |
Electroconductive rubber composition No. |
Resin Particles |
Polishing conditions |
Crown quantity [µm] |
Electron beam irradiation conditions |
Particle No. |
Number of parts [phr] |
Cutting speed [mm/min] |
Irradiation Source |
Acceleration voltage [kV] |
Electron beam dose [kGy] |
1 |
58 |
1 |
1 |
12 |
20 |
120 |
No electron beam irradiation |
2 |
59 |
1 |
1 |
12 |
20 |
120 |
Area type (FIG. 9) |
80 |
1000 |
3 |
60 |
1 |
1 |
12 |
20 |
120 |
Area type (FIG. 9) |
150 |
1000 |
4 |
61 |
5 |
- |
- |
20 |
120 |
- |
5 |
62 |
1 |
Chemical foaming |
20 |
120 |
Scanning type (FIG. 8) |
70 |
1000 |
Table 11
Example |
Roller member No. |
Surface roughness |
Height difference [µm] |
Maximum diameter [µm] |
Minimum diameter of opening [µm] |
Thickness of shell [µm] |
Rzjis [µm] |
Sm [µm] |
1 |
1 |
20 |
80 |
22 |
28 |
27 |
0.5 |
2 |
2 |
22 |
60 |
23 |
29 |
28 |
0.5 |
3 |
3 |
52 |
101 |
60 |
100 |
98 |
0.8 |
4 |
4 |
50 |
84 |
62 |
102 |
100 |
0.8 |
5 |
5 |
20 |
80 |
22 |
28 |
27 |
0.5 |
6 |
6 |
20 |
80 |
22 |
28 |
27 |
0.5 |
7 |
7 |
20 |
80 |
22 |
28 |
27 |
0.5 |
8 |
8 |
20 |
80 |
22 |
28 |
27 |
0.5 |
9 |
9 |
21 |
79 |
23 |
28 |
27 |
0.5 |
10 |
10 |
19 |
82 |
21 |
28 |
27 |
0.5 |
11 |
11 |
20 |
80 |
22 |
28 |
27 |
0.5 |
12 |
12 |
52 |
98 |
64 |
100 |
98 |
0.8 |
13 |
13 |
19 |
75 |
20 |
24 |
22 |
1 |
14 |
14 |
44 |
90 |
50 |
70 |
68 |
0.6 |
15 |
15 |
27 |
84 |
29 |
35 |
34 |
0.5 |
16 |
16 |
49 |
96 |
56 |
90 |
88 |
0.8 |
17 |
17 |
29 |
84 |
32 |
38 |
35 |
1.2 |
18 |
18 |
48 |
95 |
54 |
88 |
82 |
1.8 |
19 |
19 |
15 |
68 |
16 |
18 |
15 |
1.2 |
20 |
20 |
30 |
86 |
33 |
38 |
34 |
1.8 |
21 |
21 |
18 |
74 |
20 |
22 |
15 |
3.6 |
22 |
22 |
28 |
84 |
32 |
36 |
32 |
1.8 |
23 |
23 |
29 |
85 |
33 |
37 |
34 |
1.5 |
24 |
24 |
36 |
90 |
40 |
60 |
58 |
0.6 |
25 |
25 |
50 |
90 |
56 |
80 |
78 |
0.6 |
26 |
26 |
22 |
78 |
24 |
30 |
29 |
0.5 |
27 |
27 |
22 |
78 |
24 |
30 |
29 |
0.5 |
28 |
28 |
22 |
78 |
24 |
30 |
29 |
0.5 |
29 |
29 |
22 |
78 |
24 |
30 |
29 |
0.5 |
30 |
30 |
22 |
78 |
24 |
30 |
29 |
0.5 |
31 |
31 |
22 |
78 |
24 |
30 |
29 |
0.5 |
32 |
32 |
22 |
78 |
24 |
30 |
29 |
0.5 |
33 |
33 |
22 |
78 |
24 |
30 |
29 |
0.5 |
34 |
34 |
24 |
74 |
28 |
32 |
31 |
0.5 |
35 |
35 |
24 |
74 |
28 |
32 |
31 |
0.5 |
36 |
36 |
24 |
74 |
28 |
32 |
31 |
0.5 |
37 |
37 |
24 |
74 |
28 |
32 |
31 |
0.5 |
38 |
38 |
24 |
74 |
28 |
32 |
31 |
0.5 |
39 |
39 |
24 |
74 |
28 |
32 |
31 |
0.5 |
40 |
40 |
24 |
74 |
28 |
32 |
31 |
0.5 |
41 |
41 |
24 |
74 |
28 |
32 |
31 |
0.5 |
42 |
42 |
25 |
73 |
29 |
33 |
32 |
0.5 |
43 |
43 |
25 |
73 |
29 |
33 |
32 |
0.5 |
44 |
44 |
25 |
73 |
29 |
33 |
32 |
0.5 |
45 |
45 |
25 |
73 |
29 |
33 |
32 |
0.5 |
46 |
46 |
25 |
73 |
29 |
33 |
32 |
0.5 |
47 |
47 |
25 |
73 |
29 |
33 |
32 |
0.5 |
48 |
48 |
25 |
73 |
29 |
33 |
32 |
0.5 |
49 |
49 |
25 |
73 |
29 |
33 |
32 |
0.5 |
50 |
50 |
28 |
68 |
29 |
37 |
36 |
0.5 |
51 |
51 |
28 |
68 |
29 |
37 |
36 |
0.5 |
52 |
52 |
28 |
68 |
29 |
37 |
36 |
0.5 |
53 |
53 |
28 |
68 |
29 |
37 |
36 |
0.5 |
54 |
54 |
28 |
68 |
29 |
37 |
36 |
0.5 |
55 |
55 |
28 |
68 |
29 |
37 |
36 |
0.5 |
56 |
56 |
28 |
68 |
29 |
37 |
36 |
0.5 |
57 |
57 |
28 |
68 |
29 |
37 |
36 |
0.5 |
Table 12
Comparative Example |
Roller member No. |
Surface roughness |
Height difference [µm] |
Maximum diameter [µm] |
Minimum diameter of opening [µm] |
Thickness of shell [µm] |
Rzjis [µm] |
Sm [µm] |
1 |
58 |
20 |
80 |
24 |
28 |
27 |
0.5 |
2 |
59 |
20 |
80 |
24 |
28 |
27 |
0.5 |
3 |
60 |
20 |
80 |
24 |
28 |
27 |
0.5 |
4 |
61 |
16 |
100 |
- |
- |
- |
- |
5 |
62 |
8 |
180 |
- |
- |
- |
- |
Table 13
Example |
Roller member No. |
Restoring rate of elastic deformation [µm/sec] |
image evaluations |
End in lengthwise direction |
Middle in lengthwise direction |
1 |
2 |
Surface |
Depth from surface |
Surface |
Depth from surface |
Abrasion property |
Banding |
20 µm |
30 µm |
50 µm |
100 µm |
20 µm |
30 µm |
50 µm |
100 µm |
1 |
1 |
5.8 |
4.2 |
3.2 |
2.5 |
1 |
5.4 |
4.1 |
3.3 |
2.8 |
1.4 |
1 |
1 |
2 |
2 |
5.8 |
4.2 |
3.2 |
2.5 |
1 |
5.4 |
4.1 |
3.3 |
2.8 |
1.4 |
1 |
1 |
3 |
3 |
5.2 |
3.7 |
2.8 |
2 |
0.9 |
4.8 |
3.6 |
2.9 |
2.3 |
1.3 |
2 |
2 |
4 |
4 |
5.2 |
3.7 |
2.8 |
2 |
0.9 |
4.8 |
3.6 |
2.9 |
2.3 |
1.3 |
2 |
2 |
5 |
5 |
4.2 |
2.8 |
2 |
1.2 |
0.7 |
4 |
2.7 |
2 |
1.4 |
1 |
1 |
2 |
6 |
6 |
6.6 |
5 |
3.6 |
2.7 |
1.2 |
6 |
4.8 |
3.7 |
3 |
1.6 |
2 |
1 |
7 |
7 |
5.9 |
4 |
2.8 |
1.9 |
1 |
5.6 |
3.9 |
2.9 |
2.1 |
1.3 |
1 |
2 |
8 |
8 |
6 |
4.8 |
3.4 |
1.4 |
1.1 |
5.8 |
4.7 |
3.4 |
1.5 |
1.3 |
1 |
3 |
9 |
9 |
5.8 |
4.2 |
3.2 |
2.5 |
1 |
5.4 |
4.1 |
3.3 |
2.8 |
1.4 |
2 |
2 |
10 |
10 |
5.8 |
4.2 |
3.2 |
2.5 |
1 |
5.4 |
4.1 |
3.3 |
2.8 |
1.4 |
1 |
2 |
11 |
11 |
5.6 |
4.2 |
2.8 |
2.7 |
0.9 |
4.6 |
3.9 |
3.1 |
3.5 |
2.1 |
1 |
1 |
12 |
12 |
5.4 |
4 |
2.6 |
2.5 |
0.9 |
4.4 |
3.7 |
2.9 |
3.3 |
2.1 |
2 |
1 |
13 |
13 |
5.8 |
4.2 |
3.2 |
2.5 |
1 |
5.4 |
4.1 |
3.3 |
2.8 |
1.4 |
1 |
1 |
14 |
14 |
5.5 |
4.1 |
3 |
2.2 |
1 |
5.1 |
4 |
3.1 |
2.5 |
1.4 |
1 |
2 |
15 |
15 |
5.7 |
4.2 |
3.1 |
2.4 |
1 |
5.3 |
4.1 |
3.2 |
2.7 |
1.4 |
1 |
1 |
16 |
16 |
5.2 |
3.9 |
2.8 |
2 |
0.9 |
4.8 |
3.8 |
2.9 |
2.3 |
1.3 |
2 |
2 |
17 |
17 |
5.7 |
4 |
2.9 |
2.4 |
1.1 |
5.3 |
3.9 |
3 |
2.7 |
1.5 |
1 |
1 |
18 |
18 |
5.2 |
3.8 |
2.7 |
2 |
1 |
4.8 |
3.7 |
2.8 |
2.3 |
1.4 |
2 |
2 |
19 |
19 |
5.9 |
4.2 |
3.3 |
2.6 |
1.1 |
5.5 |
4.1 |
3.4 |
2.9 |
1.5 |
1 |
1 |
20 |
20 |
5.7 |
4 |
3.1 |
2.4 |
1 |
5.3 |
3.9 |
3.2 |
2.7 |
1.4 |
1 |
1 |
21 |
21 |
5.9 |
4.1 |
2.7 |
2.6 |
1 |
5.5 |
4 |
2.8 |
2.9 |
1.4 |
1 |
1 |
22 |
22 |
5.7 |
4 |
2.8 |
2.4 |
1 |
5.3 |
3.9 |
2.9 |
2.7 |
1.4 |
1 |
1 |
23 |
23 |
5.7 |
4.2 |
2.8 |
2.4 |
1.1 |
5.3 |
4.1 |
2.9 |
2.7 |
1.5 |
1 |
1 |
24 |
24 |
5.5 |
4.1 |
3 |
2.2 |
1 |
5.1 |
4 |
3.1 |
2.5 |
1.4 |
1 |
2 |
25 |
25 |
5.5 |
4.1 |
3 |
2.2 |
1 |
5.1 |
4 |
3.1 |
2.5 |
1.4 |
2 |
2 |
26 |
26 |
5.2 |
3.8 |
3 |
2.4 |
0.9 |
4.8 |
3.7 |
3.1 |
2.7 |
1.3 |
1 |
1 |
27 |
27 |
4 |
2.6 |
1.8 |
1.1 |
0.7 |
3.8 |
2.5 |
1.8 |
1.3 |
1 |
1 |
2 |
28 |
28 |
6.3 |
4.9 |
3.2 |
2.4 |
1 |
5.7 |
4.7 |
3.3 |
2.7 |
1.4 |
2 |
1 |
29 |
29 |
5.3 |
3.7 |
2.9 |
1.8 |
0.9 |
5 |
3.6 |
3 |
2 |
1.2 |
1 |
2 |
30 |
30 |
5.4 |
3.9 |
3 |
1.3 |
1 |
5.2 |
3.8 |
3 |
1.4 |
1.2 |
1 |
3 |
31 |
31 |
5.2 |
3.8 |
3 |
2.4 |
0.9 |
4.8 |
3.7 |
3.1 |
2.7 |
1.3 |
2 |
2 |
32 |
32 |
5.2 |
3.8 |
3 |
2.4 |
0.9 |
4.8 |
3.7 |
3.1 |
2.7 |
1.3 |
1 |
2 |
33 |
33 |
5 |
3.8 |
3 |
2.2 |
0.9 |
4 |
3.5 |
3.3 |
3 |
2.1 |
1 |
1 |
34 |
34 |
5 |
4 |
2.9 |
2.2 |
1 |
4.6 |
3.9 |
3 |
2.5 |
1.4 |
1 |
1 |
35 |
35 |
3.8 |
2.5 |
1.9 |
1 |
0.7 |
3.6 |
2.4 |
1.9 |
1.2 |
1 |
1 |
2 |
36 |
36 |
6.1 |
4.8 |
3 |
2.2 |
0.9 |
5.6 |
4.6 |
3.1 |
2.5 |
1.3 |
2 |
1 |
37 |
37 |
5.1 |
3.9 |
2.9 |
1.6 |
0.8 |
4.8 |
3.8 |
3 |
1.8 |
1.1 |
1 |
2 |
38 |
38 |
5.2 |
4 |
3 |
1.2 |
0.9 |
5 |
3.9 |
3 |
1.3 |
1.1 |
1 |
3 |
39 |
39 |
5 |
4 |
2.9 |
2.2 |
1 |
4.6 |
3.9 |
3 |
2.5 |
1.4 |
2 |
2 |
40 |
40 |
5 |
4 |
2.9 |
2.2 |
1 |
4.6 |
3.9 |
3 |
2.5 |
1.4 |
1 |
2 |
41 |
41 |
4.8 |
3.6 |
2.9 |
2.1 |
0.9 |
3.8 |
3.3 |
3.2 |
2.9 |
2.1 |
1 |
1 |
42 |
42 |
4.9 |
3.5 |
2.8 |
2.1 |
0.9 |
4.5 |
3.4 |
2.9 |
2.4 |
1.3 |
1 |
1 |
43 |
43 |
3.7 |
2.4 |
1.8 |
1 |
0.7 |
3.5 |
2.3 |
1.8 |
1.2 |
1 |
1 |
2 |
44 |
44 |
6 |
4.5 |
3.2 |
2.1 |
1.1 |
5.5 |
4.3 |
3.3 |
2.4 |
1.5 |
2 |
1 |
45 |
45 |
5 |
3.6 |
2.4 |
1.5 |
0.8 |
4.7 |
3.5 |
2.5 |
1.7 |
1.1 |
1 |
2 |
46 |
46 |
5.1 |
3.5 |
2.2 |
1.2 |
0.7 |
4.9 |
3.4 |
2.2 |
1.3 |
0.9 |
1 |
3 |
47 |
47 |
4.9 |
3.5 |
2.8 |
2.1 |
0.9 |
4.5 |
3.4 |
2.9 |
2.4 |
1.3 |
2 |
2 |
48 |
48 |
4.9 |
3.5 |
2.8 |
2.1 |
0.9 |
4.5 |
3.4 |
2.9 |
2.4 |
1.3 |
1 |
2 |
49 |
49 |
4.7 |
3.4 |
2.8 |
2.2 |
1.1 |
3.7 |
3.1 |
3.1 |
3 |
2.3 |
1 |
1 |
50 |
50 |
4.7 |
3.3 |
2.5 |
1.9 |
0.9 |
4.3 |
3.2 |
2.6 |
2.2 |
1.3 |
1 |
1 |
51 |
51 |
3.5 |
2.2 |
1.4 |
1 |
0.7 |
3.3 |
2.1 |
1.4 |
1.2 |
1 |
1 |
3 |
52 |
52 |
5.8. |
4.4 |
3 |
1.9 |
0.9 |
5.3 |
4.2 |
3.1 |
2.2 |
1.3 |
2 |
1 |
53 |
53 |
4.8 |
3.2 |
2.6 |
1.3 |
1 |
4.5 |
3.1 |
2.7 |
1.5 |
1.3 |
1 |
2 |
54 |
54 |
4.9 |
3.4 |
2.8 |
1.4 |
1.1 |
4.7 |
3.3 |
2.8 |
1.5 |
1.3 |
1 |
3 |
55 |
55 |
4.7 |
3.3 |
2.5 |
1.9 |
0.9 |
4.3 |
3.2 |
2.6 |
2.2 |
1.3 |
2 |
2 |
56 |
56 |
4.7 |
3.3 |
2.5 |
1.9 |
0.9 |
4.3 |
3.2 |
2.6 |
2.2 |
1.3 |
1 |
2 |
57 |
57 |
4.5 |
3.2 |
2.7 |
2 |
1.1 |
3.5 |
2.9 |
3 |
2.8 |
2.3 |
1 |
1 |
Table 14
Comparative Example |
Roller member No. |
Restoring rate of elastic deformation [µm/sec] |
Image evaluations |
End in lengthwise direction |
Middle in lengthwise direction |
1 |
2 |
Surface |
Depth from surface |
Surface |
Depth from surface |
Abrasion property |
Banding |
20 µm |
30 µm |
50 µm |
100 µm |
20 µm |
30 µm |
50 µm |
100 µm |
1 |
58 |
1 |
0.9 |
1 |
0.9 |
0.9 |
1 |
0.9 |
1 |
0.9 |
0.9 |
3 |
4 |
2 |
59 |
5.6 |
4.2 |
2.8 |
2.7 |
0.9 |
5.6 |
4.2 |
2.8 |
2.7 |
0.9 |
1 |
4 |
3 |
60 |
4.6 |
3.9 |
3.1 |
3.5 |
2.1 |
4.6 |
3.9 |
3.1 |
3.5 |
2.1 |
1 |
4 |
4 |
61 |
5.7 |
4 |
2.8 |
1.6 |
1.2 |
5.7 |
4 |
2.8 |
1.6 |
1.2 |
4 |
4 |
5 |
62 |
0.6 |
0.6 |
0.5 |
0.6 |
0.5 |
0.6 |
0.6 |
0.5 |
0.6 |
0.5 |
4 |
4 |
[0157] The roller member according the present invention can alleviates the concentration
of the contact pressure in a portion of the photosensitive member when the roller
member is made to come into contact with the photosensitive member. Consequently,
the non-uniform abrasion of the photosensitive member due to the contact of the roller
member can be suppressed even in use over a long term. The roller member according
to the present invention is improved in the follow-up rotation performance in relation
to the photosensitive member. Consequently, the stick-slip is made to hardly occur,
the charging unevenness of the photosensitive member and the occurrence of the banding
image due to the charging unevenness can be suppressed.
[0158] While the present invention has been described with reference to exemplary embodiments,
it is to be understood that the invention is not limited to the disclosed exemplary
embodiments. The scope of the following claims is to be accorded the broadest interpretation
so as to encompass all such modifications and equivalent structures and functions.