Charging roll
11480886 · 2022-10-25
Assignee
Inventors
- Asami UEMATSU (Fujisawa, JP)
- Atsushi Ikeda (Fujisawa, JP)
- Shogo Suzuki (Fujisawa, JP)
- Kosuke Oura (Fujisawa, JP)
- Satoshi Fukuoka (Fujisawa, JP)
- Kenji Sasaki (Fujisawa, JP)
Cpc classification
F16C2240/54
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16C2208/10
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16C13/003
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16C2202/32
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16C13/006
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16C33/203
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16C33/208
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
G03G15/0233
PHYSICS
International classification
Abstract
A charging roll includes a core member, a rubber base material disposed around the core member, and a surface layer disposed around the rubber base material. The ten point height of irregularities R.sub.Z of a surface of the surface layer is equal to or greater than 3.9 micrometers, and is equal to or less than 6.1 micrometers. The mean spacing between peaks S.sub.m of the surface of the surface layer is equal to or greater than 12.5 micrometers and is equal to or less than 13.5 micrometers.
Claims
1. A charging roll comprising: a core member; a rubber base material disposed around the core member; and a surface layer disposed around the rubber base material, a ten point height of irregularities R.sub.Z of a surface of the surface layer being equal to or greater than 3.9 micrometers and being equal to or less than 6.1 micrometers, and a mean spacing between peaks S.sub.m of the surface of the surface layer being equal to or greater than 12.5 micrometers and being equal to or less than 13.5 micrometers, wherein the surface layer comprises an electroconductive matrix comprising a base material formed an electric insulator and an electroconductive material being dispersed in the base material, and particles of a surface roughness enhancing material being dispersed in the electroconductive matrix, wherein the base material is formed of urethane resin, and wherein the particles of the surface roughness enhancing material are formed of urethane.
2. The charging roll according to claim 1, wherein the rubber base material has a ten point height irregularities Rz equal to or less than 8.5 micrometers.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
DETAILED DESCRIPTION
(4) An embodiment for carrying out the present invention will now be described in detail. In the drawings, the scale is not necessarily to scale, and some dimensions may be exaggerated for illustrative products or samples.
(5) As shown in
(6) The cylindrical and rotating photoconductor element 1 and the cylindrical and rotating charging roll 40 are in contact with each other at the nip 50. Discharge between the photoconductor element 1 and the charging roll 40 occurs in the region 51 in front of the nip 50 in the rotational direction of the photoconductor element 1 and the charging roll 40 (in some cases, in addition to discharge in the region 51 in front of the nip 50 discharge occurs in the region 52 behind the nip 50), whereby the surface of the photoconductor element 1 is charged. Preferably, the charged state of the surface of the photoconductor element 1 is uniform in both the circumferential direction and the axial direction of the photoconductor element 1.
(7)
Core Member
(8) The core member 401 can be formed of a material, including, but not limited to, a metal or resin material having excellent thermal conductivity and mechanical strength, for example, a metal material such as stainless steel, nickel (Ni), nickel alloy, iron (Fe), magnetic stainless steel, and cobalt-nickel (Co—Ni) alloy, or a resin material such as PI (polyimide resin). The structure of the core member 401 is not particularly limited, and it may be hollow or not hollow.
Rubber Base Material
(9) The rubber base material 402 is disposed on the outer peripheral surface of the core member 401, and is formed of electroconductive rubber having conductivity. The rubber base material 402 may be composed of a single layer or two or more layers. In addition, an adhesion layer, an adjustment layer, etc. may be interposed between the core member 401 and the rubber base material 402, as appropriate.
(10) The rubber base material 402 can be formed by molding a rubber composition, which is obtained by adding a conductivity imparting material, a crosslinking agent, etc. to an electroconductive rubber, around the core member 401. Examples of the electroconductive rubber include polyurethane rubber (PUR), epichlorohydrin rubber (ECO), nitrile rubber (NBR), styrene rubber (SBR), and chloroprene rubber (CR).
(11) As the conductivity imparting material, an electronic conductivity imparting material such as carbon black or metal powder, an ionic conductivity imparting material, or a mixture thereof can be used.
(12) Examples of the ionic conductivity imparting material include organic salts, inorganic salts, metal complexes, and ionic liquids. An example of an organic salt is sodium trifluoride acetate, and examples of the inorganic salt includes lithium perchlorate and quaternary ammonium salt. An example of a metal complex is ferric halide-ethylene glycol, and specific examples thereof include those described in JP-B-3655364. The ionic liquid is a molten salt that is liquid at room temperature, and is referred to as a room temperature molten salt. The salt has a melting point of 70 degrees Celsius or less, preferably 30 degrees Celsius or less. Specific examples thereof include those described in JP-A-2003-202722.
(13) The crosslinking agent is not particularly limited, and examples thereof include sulfur and a peroxide vulcanizing agent.
(14) Furthermore, a crosslinking aid, etc. that promotes action of the crosslinking agent may be added to the rubber composition, as appropriate. Examples of the crosslinking aid include inorganic materials, such as zinc oxide and magnesium oxide, and organic materials, such as stearic acid and amines. In addition, to shorten a time taken to achieve crosslinking, a thiazole-based or other crosslinking accelerator may be used. Other additives may be added to the rubber composition, as appropriate.
(15) In this embodiment, the surface of the rubber base material 402 formed on the outer peripheral surface of the core member 401 is first ground to a predetermined thickness with a grinding machine, after which the surface of the rubber base material 402 is subjected to dry grinding with a grinding wheel. The surface layer 403 is then formed on the outer peripheral surface of the rubber base material 402. Grinding is performed to adjust the surface roughness of the rubber base material 402 as appropriate, and to thereby adjust the surface roughness of the surface layer 403 formed on the outer peripheral surface of the rubber base material 402.
(16) In a case in which the surface roughness of the rubber base material 402 is to be minimized, the surface roughness (ten-point height irregularities) R.sub.Z according to JIS B 0601 (1994) of the rubber base material 402 is preferably equal to or less than 8.5 micrometers. The surface roughness R.sub.Z is measured by a contact-type surface roughness meter.
(17) Dry grinding is performed, for example, in a state in which the rubber base material 402 is rotated, by moving the rotary grinding wheel along the axial direction of the core member 401 while the wheel is in contact with the rubber base material 402 (traverse grinding). In a case in which the surface roughness of the rubber base material 402 is to be minimized, the number of revolutions of the grinding wheel of the grinding machine may be gradually increased, for example, from 1000 rpm, to 2000 rpm, to 3000 rpm. Alternatively, the coarseness of a grinding wheel may be progressively changed. For example, a GC (green carborundum) grinding wheel may be changed, for example, from a GC 60 wheel, to a GC 120 wheel, to a GC 220 wheel.
(18) In addition, after the surface of the rubber base material 402 is dry-ground, the surface may be wet ground with a wet grinding machine in which a waterproof grinding paper such as waterproof sandpaper is employed, with the rubber base material 402 being brought into contact with the sandpaper under supply of a grinding liquid.
Rubber Hardness of Rubber Base Material
(19) The rubber hardness of the base material 402 is measured by use of a durometer “Type A” according to JIS K 6253 and ISO 7619, and the hardness is preferably within a range from 50 degrees to 64 degrees.
(20) The surface layer 403 formed on the rubber base material 402 is thin, and thus the hardness of the surface of the charging roll 40 is affected by a hardness of the rubber base material 402. In a case in which the hardness of the rubber base material 402 is less than 50 degrees, convex portions on the surface of the charging roll 40 are likely to be crushed and contaminate the photoconductor element 1, and cause image defects. On the other hand, if the hardness of the rubber base material 402 is greater than 64 degrees, convex portions on the surface of the charging roll 40 may affect the image.
Surface Layer
(21) In this embodiment, a coating liquid is applied to the outer peripheral surface of the rubber base material 402 and dried and cured, thereby forming the surface layer 403. Application of the coating liquid may be carried out by dip coating, roll coating, spray coating, or the like.
(22) As shown in
(23) In the example shown in
(24) In the present embodiment, the surface roughness of the surface layer 403 is adjusted by dispersing the particles 405 of the roughness enhancing material in the surface layer 403 formed on the rubber base material 402, of which the surface roughness is adjusted.
(25) In the present embodiment, it would be preferable for the thickness of the electroconductive matrix 404 of the surface layer 403 to be within an appropriate numerical range. It is contemplated that if the thickness is too large, the surface roughness of the surface layer 403 will be too small resulting in image unevenness.
(26) Furthermore, in the present embodiment, it would be preferable for the amount of the particles 405 of the roughness enhancing material in the surface layer 403 to be within an appropriate numerical range. It is contemplated that if the amount of the particles is large, the particles may overlap, causing the surface of the surface layer 403 to be rough, and resulting image unevenness.
(27) In this embodiment, the composition of the coating liquid that is the material of the surface layer 403 contains at least the base material, the electroconductive material, and the particles 405 of the surface roughness enhancing material. After curing of the coating liquid, the base material and the electroconductive material become components of the electroconductive matrix 404.
(28) The coating liquid is obtained, for example, by dissolving in a diluent solvent the following components.
Composition of Coating Liquid
(29) Base material, 10 to 80 parts by weight;
(30) electroconductive material, 1 to 50 parts by weight; and
(31) surface roughness enhancing material, 70% by weight or less of the total amount of the coating liquid.
(32) It is contemplated that when the surface roughness and the pitches of irregularities of the surface layer 403 are appropriate, discharge between the charging roll 40 and the photoconductor element 1 will be substantially uniform in the gap before the nip, at which the charging roll 40 and the photoconductor element 1 are in contact with each other, so that uneven discharge will not occur upon image formation, whereby an image of a desired density will be formed, with an end result of provision of high image quality.
(33) It is considered that the surface roughness and the pitches of irregularities of the surface layer 403 can be adjusted as appropriate by adjusting the particle diameter and the amount of the particles 405 of the surface roughness enhancing material.
Base Material
(34) The base material contained in the coating liquid is an electric insulator. Examples of the base material include urethane resin, acrylic resin, acrylic urethane resin, amino resin, silicone resin, fluorine resin, polyamide resin, epoxy resin, polyester resin, polyether resin, phenol resin, urea resin, polyvinylbutyral resin, melamine resin, nylon resin, etc. The base materials may be used alone or in combination.
Electroconductive Material
(35) Examples of the electroconductive material contained in the coating liquid include a carbon black such as acetylene black, Ketjen black, and Tokablack, a carbon nanotube, an ion such as lithium perchloride, an ionic liquid such as 1-butyl-3-methylimidazolium hexafluorophosphate, and a metal oxide such as tin oxide, and an electroconductive polymer. These electroconductive materials may be used alone or in combination.
Surface Roughness Enhancing Material
(36) Examples of the particles 405 of the surface roughness enhancing material contained in the coating liquid include acrylic particles, urethane particles, polyamide resin particles, silicone resin particles, fluororesin particles, styrene resin particles, phenol resin particles, polyester resin particles, olefin resin particles, epoxy resin particles, nylon resin particles, carbon, graphite, carbide balloon, silica, alumina, titanium oxide, zinc oxide, magnesium oxide, zirconium oxide, calcium sulfate, calcium carbonate, magnesium carbonate, calcium silicate, aluminum nitride, boron nitride, talc, kaolin clay, diatomaceous earth, glass beads, hollow glass spheres, etc. These particles may be used alone or in combination.
Relationship Between Content Percentage and Particle Diameter
(37) It is considered that there is a preferable range with respect to the relationship between the particle diameter and the amount of the particles 405 of the surface roughness enhancing material in the coating liquid in order to improve the image quality.
Diluent Solvent
(38) The diluent solvent contained in the coating liquid is not particularly limited, and examples thereof include an aqueous-based solvent or other solvents such as methyl acetate, ethyl acetate, butyl acetate, methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK), methanol, ethanol, butanol, 2-propanol (IPA), acetone, toluene, xylene, hexane, heptane, and chloroform.
Working Examples
(39) Experiments were conducted to investigate characteristics of the charging roll 40 suitable for reducing image unevenness.
Experiment 1
(40) In Experiment 1, samples 1-4 of the charging roll 40 according to the embodiment were produced.
Preparation of Rubber Base Material
(41) A rubber composition obtained by adding 0.5 parts by weight of sodium trifluoroacetate (as a conductivity imparting material), 3 parts by weight of zinc oxide, 2 parts by weight of stearic acid, and 1.5 parts by weight of a crosslinking agent to 100 parts by weight of epichlorohydrin rubber (“Epichlomer CG-102” manufactured by Osaka Soda Co., Ltd., Osaka, Japan) was kneaded with a roll mixer.
(42) The kneaded rubber composition was formed into a sheet material and wound around the surface of a core member 401 having a diameter of 6 mm. The sheet material was press-molded to form a rubber base material 402 made of crosslinked epichlorohydrin rubber.
(43) The hardness of the resulting rubber base material 402 was measured using a durometer “Type A” according to JIS K 6253 and ISO 7619. The measured hardness was within a range from 50 degrees to 64 degrees.
Grinding Surface of Rubber Base Material
(44) The surface of the rubber base material 402 was ground with a grinding machine. More specifically, the surface of the obtained rubber base material 402 was ground with a grinding machine to provide the rubber base material 402 with a predetermined thickness (1.25 mm), followed by dry grinding in which the rotation speed of the grinding wheel of the grinding machine was gradually increased from 1000 rpm, to 2000 rpm, to 3000 rpm. That is, in Experiment 1, the surface roughness of the rubber base material 402 was minimized.
Preparation of Coating Liquid
(45) A coating liquid for forming the surface layer 403 on the outer peripheral surface of the rubber base material 402 described above was prepared.
Composition of Coating Liquid
(46) The composition of the coating liquid is as shown in Table 1.
(47) TABLE-US-00001 TABLE 1 Composition of Coating Liquid Ratio Material (Parts by Function Material Details Weight) Diluent Ethyl Acetate 60.0 Solvent Base Urethane Resin 19.9 Material Contents of Base Material Polyol “T5650E” Manufactured by Asahi Kasel Chemicals Corp. 10.8 (Tokyo, Japan) lsocyanurate “TPA-100” Manufactured by 9.1 Asahi Kasei Chemicals Corp. (Tokyo, Japan) Electro- Carbon Dispersed “MHI-BK” (Including 20 to 30 18.4 conductive Liquid Weight % of Carbon) Material Manufactured by Mikuni Color Ltd. (Hyogo, Japan) Additive Acrylic Silicone “MODIPER FS-700” 1.0 Polymer Manufactured by NOF Corp. (Tokyo, Japan) Surface Urethane Particles Urethane Beads Manufactured See Roughness by Negami Chemical Industrial Table 2 Enhancing Co., Ltd. (Tokyo, Japan) Material
(48) Urethane beads manufactured by Negami Chemical Industrial Co., Ltd. (Tokyo, Japan) were used as the urethane particles.
(49) The relationship between the average particle diameter of the urethane beads and the product name used in Experiments 1 and 2 is as follows. It is of note that in practice, one product contains particles having diameters that differ from the average particle diameter.
(50) 6 micrometers: Urethane beads “C-800”
(51) 10 micrometers: Urethane beads “C-600”
(52) 15 micrometers: Urethane beads “C-400”
(53) In Experiment 1, samples 1-4 having different surface conditions of the surface layer 403 were produced by applying coating liquids containing particles 405 of the surface roughness enhancing material having different particle diameters and in different amounts. The surface roughness and the pitches of irregularities of the surface layer 403 in the samples are as shown in Table 2.
(54) The coating liquid having the above composition was stirred with a ball mill for 3 hours.
(55) TABLE-US-00002 TABLE 2 Surface Roughness Enhancing Material R.sub.z of S.sub.m of Average Content Image Unevenness Image Surface Surface Particle Percentage In Local Comprehensive Layer Layer Diameter Coating Liquid Discharge Scumming Judgment [μm] [μm] [μm] [wt %] — — — Sample 1 3.9 13.0 10 2 Good Good Good Sample 2 6.1 13.0 6 2 Good Good Good Sample 3 2.2 10.5 10 2 Bad Bad Bad Sample 4 2.5 16.1 15 2 Bad Bad Bad Sample 5 9.8 21.2 6 15 Bad Good Bad
Preparation of Charging Roll
(56) The surface layer 403 was formed by applying the coating liquid to the outer peripheral surface of the ground rubber base material 402, to manufacture a charging roll 40. Specifically, the coating liquid was stirred, and the liquid was spray-coated on the surface of the rubber base material 402, and dried in an electric furnace at 120 degrees Celsius for 60 minutes to form the surface layer 403 on the outer peripheral surface of the rubber base material 402, to produce a charged roll.
Measurement of Surface Roughness R.SUB.Z
(57) Using a contact-type surface roughness measuring machine (Surf Coder “SE500” manufactured by Kosaka Laboratory Ltd. (Tokyo, Japan)), the surface roughness (ten point height of irregularities) R.sub.Z (conforming to JIS B 0601: 1994) of the surface layer 403 was measured under the measurement conditions described below. The measurement results are shown in Table 2.
Measurement Conditions
(58) Cutoff: λc=0.8 mm
(59) Measurement length: 4 mm (sampling length method)
(60) Measurement speed: 0.5 mm/sec
(61) Measurement positions: Surface roughness R.sub.Z was measured at 3 points of each charging roll 40. Then, the average of these values was calculated. The average value is shown in Table 2.
Measurement of Mean Spacing Between Peaks S.SUB.m
(62) The mean spacing between peaks S.sub.m at the surface of the surface layer 403 (conforming to JIS B 0601:1994) was measured.
(63) First, two portions of the surface of the central part in the axial direction of the charging roll 40 was photographed with a non-contact type laser microscope. The laser microscope used was a “VK-X200” manufactured by Keyence Corporation (Osaka, Japan). Magnification was 400 times, and the photographic field of view of each of the two portions was 528.7 micrometers along the circumferential direction of the charging roll 40 and was 705.1 micrometers along the axial direction of the charging roll 40.
(64) Next, using Version 1 2.0.116 of the multi-file analysis application “VK-H1XM” produced by Keyence Corporation, the value S.sub.m was calculated for 19 lines at equal intervals in each field of view photographed. Each line was along the axial direction. The cutoff value λc was 0.8 mm. Furthermore, these values S.sub.m were averaged. Table 2 shows the average of values S.sub.m.
Evaluation of Image Unevenness and Discharge Unevenness
(65) An image evaluation test of the samples of the charging roll was conducted using a copying machine. The copying machine was a color multifunction peripheral (MFP) “bizhub C3850” (DC-voltage supply type) manufactured by Konica Minolta Inc. (Tokyo, Japan).
(66) The applied charging voltage was measured with a tester. In Experiment 1, a voltage (REF−100 V), which was 100 V lower than the normal voltage (REF), was applied by way of an external power supply.
(67) The charging roll was applied to the copying machine, and image unevenness was evaluated for images (halftone images and white solid images) printed under the conditions described below. The results are shown in Table 2.
(68) For the image unevenness evaluation, occurrence of local discharge was judged on the basis of the halftone images, and lightness was judged on the basis of the white solid images. Occurrence of local discharge was confirmed by visual detection of white spots, black spots, white streaks, or black streaks in the halftone images.
Printing Conditions
(69) Speed: 38 sheets/minute
(70) Printing environment: The temperature was 23 degrees Celsius and the humidity was 55%.
Local Discharge Evaluation
(71) For the halftone images, occurrence of image unevenness caused by local discharge was evaluated by visual observation using the following criteria.
(72) Good: No image unevenness caused by local discharge.
(73) Bad: Image unevenness caused by local discharge.
Lightness Determination
(74) The L* value (lightness) was measured at seven points in each solid white image by a chroma meter, “CR-400” manufactured by Konica Minolta Inc. The lightness was evaluated with the following evaluation criteria. The reason why the lightness was measured was to determine whether scumming, i.e., fogging (printing on a non-print area) occurred.
Evaluation Criteria
(75) Good: No scumming. (L* is 95.5 or more)
(76) Bad: Scumming. (L* is lower than 95.5)
(77) Samples in which image unevenness occurred due to local discharge or scumming were judged to be bad in image comprehensive judgment, and samples in which image unevenness or scumming did not occur were judged to be good in image comprehensive judgment. These were described in Table 2.
Experiment 2
(78) In Experiment 2, sample 5 of the charging roll 40 according to the embodiment was produced.
Preparation of Rubber Base Material
(79) The rubber base material was the same as that in Experiment 1.
Grinding Surface of Rubber Base Material
(80) The surface of the rubber base material 402 was ground with a grinding machine. More specifically, the surface of the obtained rubber base material 402 was ground with a grinding machine to provide the rubber base material 402 with a predetermined thickness (2 mm), after which dry grinding was applied. In Experiment 2, the rotation speed of the grinding wheel was not changed.
Preparation of Coating Liquid
(81) A coating liquid for forming the surface layer 403 on the outer peripheral surface of the rubber base material 402 described above was prepared.
Composition of Coating Liquid
(82) The composition of the coating liquid is shown in Table 1.
(83) Urethane beads manufactured by Negami Chemical Industrial Co., Ltd. (Tokyo, Japan) were used as the urethane particles.
(84) In Experiment 2, sample 5 was produced by applying coating liquids containing particles 405 of the surface roughness enhancing material having the particle diameter and the amount in Table 2. The surface roughness and the pitches of irregularities of the surface layer 403 in sample 5 are as shown in Table 2.
(85) The coating liquid having the above composition was stirred with a ball mill for 3 hours.
Preparation of Charging Roll
(86) In the same manner as that of Experiment 1, the surface layer 403 was formed by applying the coating liquid to the outer peripheral surface of the ground rubber base material 402, to manufacture a charging roll 40.
Measurement of Surface Roughness R.SUB.Z
(87) Using the same procedure as in Experiment 1, the surface roughness (ten point height of irregularities) R.sub.Z on the surface of the surface layer 403 was measured. The ten point height of irregularities R.sub.Z is shown in Table 2.
Measurement of Mean Spacing Between Peaks S.SUB.m
(88) Using the same procedure as in Experiment 1, the mean spacing between peaks S.sub.m at the surface of the surface layer 403 (conforming to JIS B 0601:1994) was measured.
Evaluation of Image Unevenness and Discharge Unevenness
(89) An image evaluation test of the samples of the charging roll was conducted using a copying machine. The copying machine was a color multifunction peripheral (MFP) “MP C5503” (AC/DC voltage-superimposed supply type) manufactured by Ricoh Company, Ltd. (Tokyo, Japan).
(90) The DC voltage was the normal voltage (REF), and the AC voltage V.sub.pp was controlled by the copying machine.
(91) In Experiment 2, the alternating current was set at 1.40 mA, which is lower than the normal alternating current (REF) of the copying machine.
(92) The charging roll was applied to the copying machine, and the image unevenness was evaluated for images (halftone images and white solid images) printed under the following printing conditions. The results are shown in Table 2. For the image unevenness evaluation, occurrence of local discharge was judged on the basis of the halftone images. Occurrence of local discharge was confirmed by visual detection of white spots, black spots, white streaks, or black streaks in the halftone images. Occurrence of scumming, i.e., fogging was judged by visual detection in the white solid images.
Printing Conditions
(93) Speed: 30 sheets/minute
(94) Printing environment: The temperature was 23 degrees Celsius and the humidity was 55%.
Local Discharge Evaluation
(95) For the halftone images, occurrence of image unevenness caused by local discharge was judged by visual observation using the following criteria.
(96) Good: No image unevenness caused by local discharge.
(97) Bad: Image unevenness caused by local discharge.
Determination of Scumming
(98) For the white solid images, occurrence of scumming, i.e., fogging (printing on a no-print area) was judged by visual observation.
(99) Evaluation Criteria
(100) Good: No scumming.
(101) Bad: Scumming.
(102) Although scumming did not occur in sample 5, image unevenness caused by local discharge occurred in sample 5. Accordingly, sample 5 was judged to be bad in image comprehensive judgment.
(103) As will be apparent from Table 2, it is preferable for the ten point height of irregularities R.sub.Z of the surface of the surface layer 403 to be equal to or greater than 3.9 micrometers and to be equal to or less than 6.1 micrometers, and it is preferable for the mean spacing between peaks S.sub.m of the surface of the surface layer 403 to be 13.0 micrometers. However, considering the measurement error, it is preferable for the mean spacing between peaks S.sub.m of the surface of the surface layer 403 to be equal to or greater than 12.5 micrometers and to be equal to or less than 13.5 micrometers.