JP2008020634A - Image formation roller - Google Patents
Image formation roller Download PDFInfo
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- JP2008020634A JP2008020634A JP2006191908A JP2006191908A JP2008020634A JP 2008020634 A JP2008020634 A JP 2008020634A JP 2006191908 A JP2006191908 A JP 2006191908A JP 2006191908 A JP2006191908 A JP 2006191908A JP 2008020634 A JP2008020634 A JP 2008020634A
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- shaft
- resin
- image forming
- conductive
- coating layer
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- 230000015572 biosynthetic process Effects 0.000 title abstract 4
- 229920005989 resin Polymers 0.000 claims abstract description 59
- 239000011347 resin Substances 0.000 claims abstract description 59
- 239000010410 layer Substances 0.000 claims abstract description 31
- 239000011247 coating layer Substances 0.000 claims abstract description 26
- 239000004020 conductor Substances 0.000 claims abstract description 14
- 239000011342 resin composition Substances 0.000 claims abstract description 13
- 239000004760 aramid Substances 0.000 claims abstract description 12
- 229920003235 aromatic polyamide Polymers 0.000 claims abstract description 12
- 239000004953 Aliphatic polyamide Substances 0.000 claims abstract description 10
- 229920003231 aliphatic polyamide Polymers 0.000 claims abstract description 10
- 239000003365 glass fiber Substances 0.000 claims abstract description 10
- 239000013013 elastic material Substances 0.000 claims abstract description 9
- 230000002093 peripheral effect Effects 0.000 claims abstract description 9
- 229920001971 elastomer Polymers 0.000 claims description 19
- 239000005060 rubber Substances 0.000 claims description 19
- 238000010894 electron beam technology Methods 0.000 claims description 16
- 238000005452 bending Methods 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 9
- 229920002379 silicone rubber Polymers 0.000 claims description 8
- 239000004945 silicone rubber Substances 0.000 claims description 8
- 229920000181 Ethylene propylene rubber Polymers 0.000 claims description 4
- 229920000459 Nitrile rubber Polymers 0.000 claims description 4
- 229920006311 Urethane elastomer Polymers 0.000 claims description 4
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 4
- QWYSJTTWCUXHQO-UHFFFAOYSA-N [F].OC(=O)C=C Chemical compound [F].OC(=O)C=C QWYSJTTWCUXHQO-UHFFFAOYSA-N 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims 1
- 238000003384 imaging method Methods 0.000 claims 1
- 238000005498 polishing Methods 0.000 abstract description 13
- 239000000203 mixture Substances 0.000 description 14
- 230000009477 glass transition Effects 0.000 description 12
- 239000000178 monomer Substances 0.000 description 7
- 239000006229 carbon black Substances 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 229920000049 Carbon (fiber) Polymers 0.000 description 3
- 239000004917 carbon fiber Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229920006121 Polyxylylene adipamide Polymers 0.000 description 2
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- -1 polymethylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 241000287462 Phalacrocorax carbo Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 231100000987 absorbed dose Toxicity 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- CHIHQLCVLOXUJW-UHFFFAOYSA-N benzoic anhydride Chemical compound C=1C=CC=CC=1C(=O)OC(=O)C1=CC=CC=C1 CHIHQLCVLOXUJW-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical class O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000003273 ketjen black Substances 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000006234 thermal black Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Landscapes
- Electrophotography Configuration And Component (AREA)
- Electrostatic Charge, Transfer And Separation In Electrography (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Dry Development In Electrophotography (AREA)
- Cleaning In Electrography (AREA)
Abstract
Description
本発明は、複写機、プリンター、ファクシミリ等の電子写真方式に基づく画像形成装置の作像部に使用される作像ローラに係り、特に、樹脂系シャフトを備える作像ローラに関する。 The present invention relates to an image forming roller used in an image forming unit of an image forming apparatus based on an electrophotographic system such as a copying machine, a printer, and a facsimile, and more particularly to an image forming roller including a resin shaft.
複写機、プリンター、ファクシミリ等の電子写真方式に基づく画像形成装置の作像部には、転写ローラ、トナー供給ローラ、現像ローラ、クリーニングローラ等作像に関与する作像ローラが使用されている。従来、そのような作像ローラは、金属製のシャフトの外周に導電性弾性層を設けた構成のものであるが、近年、画像形成装置の小型化、軽量化等の要請により、シャフトを樹脂組成物で形成することが試みられている。例えば、特許文献1および特許文献2には、ポリアミド等の合成樹脂および導電剤と、場合により繊維を含む樹脂組成物からなる非磁性現像ローラが開示されている。また、特許文献3には、ポリアミド樹脂と導電性材料を含む導電性樹脂組成物からなるシャフトを備える現像ローラが開示されている。 In an image forming unit of an image forming apparatus based on an electrophotographic system such as a copying machine, a printer, or a facsimile, an image forming roller related to image forming such as a transfer roller, a toner supply roller, a developing roller, and a cleaning roller is used. Conventionally, such an image forming roller has a configuration in which a conductive elastic layer is provided on the outer periphery of a metal shaft. However, in recent years, due to demands for reducing the size and weight of image forming apparatuses, the shaft is made of resin. Attempts have been made to form with compositions. For example, Patent Document 1 and Patent Document 2 disclose a nonmagnetic developing roller made of a resin composition containing a synthetic resin such as polyamide and a conductive agent, and optionally fibers. Patent Document 3 discloses a developing roller having a shaft made of a conductive resin composition containing a polyamide resin and a conductive material.
しかしながら、従来の樹脂系シャフトは、上記特許文献2に記載されているように、樹脂系シャフトを配設した金型内で導電性弾性材料を発泡させることだけによるか、発泡させた導電性弾性材を所定形状に成形した後、これを樹脂系シャフトに接着することだけにより、導電性弾性層を設ける場合や、上記特許文献3に記載されているように、樹脂系シャフトに半導電性材をコーティングするだけにより半導電性層を設ける場合には、問題はないが、樹脂系シャフトの外周に導電性弾性材料を押し出し等により被覆した後、樹脂系シャフトのジャーナル部でシャフトを支持し、被覆した導電性弾性材料を研磨して導電性弾性層を形成する場合には、研磨の際に樹脂系シャフトがジャーナル部で破壊してしまい、作像ローラを作製できないという問題が生じる。 However, as described in Patent Document 2, the conventional resin-based shaft is obtained by foaming a conductive elastic material in a mold provided with the resin-based shaft or by foaming. After forming the material into a predetermined shape, the conductive elastic layer is provided only by adhering the material to the resin-based shaft, or as described in Patent Document 3, the semi-conductive material is provided on the resin-based shaft. There is no problem when a semiconductive layer is provided only by coating, but after covering the outer periphery of the resin shaft with a conductive elastic material, etc., the shaft is supported by the journal portion of the resin shaft, When polishing the coated conductive elastic material to form a conductive elastic layer, the resin shaft is destroyed at the journal during polishing, and an image forming roller cannot be manufactured. Cormorant problem arises.
また、作像ローラは、上述のようにシャフトの外周に導電性弾性層が形成されるが、導電性弾性層の上には、弾性層の汚染の防止、耐摩耗性の向上、トナーに対する帯電性の最適化等を目的として、樹脂被覆層を設けることが一般である。しかし、シャフトを樹脂で形成した場合、樹脂被覆層の形成の際に適用される熱の影響で、作像ローラの寸法精度が低下し、振れ精度が低下してしまうことがわかった。
したがって、本発明は、樹脂系シャフトを有しながら、導電性弾性材料の研磨加工によって破損することがなく、しかも樹脂被覆層の形成後も寸法精度の低下が抑制された作像ローラを提供することを目的とする。 Accordingly, the present invention provides an image forming roller having a resin-based shaft, which is not damaged by polishing of a conductive elastic material, and in which a reduction in dimensional accuracy is suppressed even after a resin coating layer is formed. For the purpose.
本発明によれば、芳香族ポリアミド、ガラス繊維、導電材および任意に脂肪族ポリアミドを含む樹脂組成物から形成され、250MPa以上の曲げ強度および15GPa以上の曲げ弾性率を示すシャフトと、このシャフトの外周面を覆って設けられ、表面が研磨加工された導電性弾性層と、この導電性弾性層の外周面を覆って設けられた被覆層を備え、前記被覆層は、紫外線硬化樹脂または電子線硬化樹脂を含むことを特徴とする作像ローラが提供される。 According to the present invention, a shaft formed of a resin composition containing an aromatic polyamide, glass fiber, a conductive material, and optionally an aliphatic polyamide, having a bending strength of 250 MPa or more and a bending elastic modulus of 15 GPa or more, and the shaft A conductive elastic layer provided so as to cover the outer peripheral surface and having a polished surface, and a coating layer provided so as to cover the outer peripheral surface of the conductive elastic layer, the coating layer comprising an ultraviolet curable resin or an electron beam An image forming roller is provided that includes a cured resin.
本発明の作像ローラは、シャフトが樹脂組成物で形成されたものでありながら、導電性弾性材料の研磨加工によって破損することがなく、しかも被覆層の形成後も寸法精度の低下が抑制されている。 In the image forming roller of the present invention, although the shaft is formed of a resin composition, it is not damaged by polishing of the conductive elastic material, and the decrease in dimensional accuracy is suppressed even after the coating layer is formed. ing.
本発明に係る作像ローラは、芳香族ポリアミド、ガラス繊維、および導電材粒子を含む樹脂組成物から形成されたシャフトを有し、このシャフトの外周に導電性弾性層が設けられている。導電性弾性層の外周面には、所定の樹脂被覆層が形成されている。 The image forming roller according to the present invention has a shaft formed of a resin composition containing aromatic polyamide, glass fiber, and conductive material particles, and a conductive elastic layer is provided on the outer periphery of the shaft. A predetermined resin coating layer is formed on the outer peripheral surface of the conductive elastic layer.
本発明に係る作像ローラの樹脂系シャフトは、250MPa以上の曲げ強度および15GPa以上の曲げ弾性率を示す。曲げ強度および曲げ弾性率がこれら値未満であると、シャフトに導電性ゴム等の導電性弾性層を設けた後、その導電性弾性層を砥石等で研削・研磨する際に割れ等が発生し得る。曲げ強度は、通常、500MPa以下であり、曲げ弾性率は、通常、30GPa以下である。 The resin shaft of the image forming roller according to the present invention exhibits a bending strength of 250 MPa or more and a bending elastic modulus of 15 GPa or more. If the bending strength and flexural modulus are less than these values, cracks will occur when a conductive elastic layer such as conductive rubber is provided on the shaft and then the conductive elastic layer is ground and polished with a grindstone. obtain. The bending strength is usually 500 MPa or less, and the bending elastic modulus is usually 30 GPa or less.
本発明に係る作像ローラのシャフトは、さらに、70℃以上のガラス転移点を示すことが好ましい。作像ローラは、通常、ユニットとして組み立てられ、応力のかかった状態で60℃程度で保存されることが多い。また、ジャーナル部の切削加工時に60℃程度の温度に加熱されることがある。ガラス転移点が70℃未満であると、上記保存時にたわみが発生する可能性があり、また上記切削加工時に変形し、表面精度が低下するおそれがある。ガラス転移点は、通常、100℃以下である。 The shaft of the image forming roller according to the present invention preferably further exhibits a glass transition point of 70 ° C. or higher. The image forming roller is usually assembled as a unit and stored at about 60 ° C. in a stressed state. Further, the journal part may be heated to a temperature of about 60 ° C. during the cutting process. When the glass transition point is less than 70 ° C., there is a possibility that deflection occurs during the storage, and deformation occurs during the cutting process, which may reduce the surface accuracy. The glass transition point is usually 100 ° C. or lower.
また、本発明に係る作像ローラのシャフトは、さらに、1.8以下の比重を示すことが好ましい。比重が1.8を超えると、軽量化の要請に十分に応えることができないおそれがある。比重は、通常、1.0以上である。 The shaft of the image forming roller according to the present invention preferably further exhibits a specific gravity of 1.8 or less. If the specific gravity exceeds 1.8, there is a possibility that the request for weight reduction cannot be sufficiently met. The specific gravity is usually 1.0 or more.
さらに、本発明に係る作像ローラのシャフトは、1×105Ω・cm以下の体積抵抗率を示すことが好ましい。1×105Ω・cmを超える体積抵抗率は、シャフトの外周に設けられる導電性弾性層に必要な抵抗値よりも高くなり、印字に悪影響を及ぼす恐れがある。体積抵抗率は、通常、1×100Ω・cm以上である。 Furthermore, the shaft of the image forming roller according to the present invention preferably exhibits a volume resistivity of 1 × 10 5 Ω · cm or less. The volume resistivity exceeding 1 × 10 5 Ω · cm is higher than the resistance value required for the conductive elastic layer provided on the outer periphery of the shaft, which may adversely affect printing. The volume resistivity is usually 1 × 10 0 Ω · cm or more.
上記物性を示すシャフトは、上述のように、芳香族ポリアミド、ガラス繊維、および導電材粒子を含み、脂肪族ポリアミドをさらに含み得る樹脂組成物から形成されるものである。 As described above, the shaft having the above physical properties is formed from a resin composition that includes aromatic polyamide, glass fiber, and conductive material particles, and may further include aliphatic polyamide.
芳香族ポリアミドは、主鎖に芳香族基を有するポリアミドであり、メタキシリレンジアミンと、アジピン酸、コハク酸、グルタル酸、ピメリン酸等のα,ω−脂肪族ジカルボン酸との重縮合反応により得られるものである。メタキシリレンジアミンとアジピン酸とから得られる芳香族ポリアミドは、ポリアミドMXD6として知られている。 The aromatic polyamide is a polyamide having an aromatic group in the main chain, and is obtained by a polycondensation reaction between metaxylylenediamine and an α, ω-aliphatic dicarboxylic acid such as adipic acid, succinic acid, glutaric acid or pimelic acid. It is obtained. An aromatic polyamide obtained from metaxylylenediamine and adipic acid is known as polyamide MXD6.
脂肪族ポリアミドは、ヘキサメチレンジアミン等のポリメチレンジアミンと脂肪族ジカルボン酸との重縮合物の構造を有し、ポリアミド6、ポリアミド6,6等が含まれる。 The aliphatic polyamide has a polycondensate structure of polymethylene diamine such as hexamethylene diamine and an aliphatic dicarboxylic acid, and includes polyamide 6, polyamide 6,6 and the like.
ガラス繊維としては、それ自体既知のものを用いることができる。ガラス繊維の直径は、1〜50μmであることが好ましく、またその長さは、0.1〜10mmであることが好ましい。 As the glass fiber, those known per se can be used. The diameter of the glass fiber is preferably 1 to 50 μm, and the length is preferably 0.1 to 10 mm.
導電材としては、チャンネルブラック、ファーネスブラック、サーマルブラック、ランプブラック、ケッチェンブラック、アセチレンブラック等のカーボンブラックや、炭素繊維等を好適に用いることができる。炭素繊維の直径は、1〜50μmであることが好ましく、またその長さは、0.1〜10mmであることが好ましい。導電材としては、カーボンブラックと炭素繊維を併用することができる。 As the conductive material, carbon black such as channel black, furnace black, thermal black, lamp black, ketjen black, and acetylene black, carbon fiber, and the like can be suitably used. The diameter of the carbon fiber is preferably 1 to 50 μm, and the length is preferably 0.1 to 10 mm. As the conductive material, carbon black and carbon fiber can be used in combination.
上記樹脂組成物は、シャフトに上記物性をもたらすために、芳香族ポリアミドと脂肪族ポリアミドとの合計100質量部に対し、ガラス繊維を10〜300質量部、導電材を0.1〜20質量部の割合で含有することが好ましい。芳香族ポリアミドと脂肪族ポリアミドの質量比は、100:0〜50:50であることが好ましい。 In order to bring the physical properties to the shaft, the resin composition has a glass fiber of 10 to 300 parts by mass and a conductive material of 0.1 to 20 parts by mass with respect to a total of 100 parts by mass of the aromatic polyamide and the aliphatic polyamide. It is preferable to contain in the ratio. The mass ratio of the aromatic polyamide and the aliphatic polyamide is preferably 100: 0 to 50:50.
本発明の作像ローラのシャフトは、射出成形等の方法により成形することができる。射出成形後、ジャーナル部を切削加工で仕上げることができる。すなわち、より詳しくは、本発明の作像ローラのシャフトは、シャフト本体と、シャフト本体の両端にそれぞれ一体的に設けられたジャーナル部を有する。 The shaft of the image forming roller of the present invention can be formed by a method such as injection molding. After injection molding, the journal part can be finished by cutting. More specifically, the shaft of the image forming roller of the present invention has a shaft main body and journal portions integrally provided at both ends of the shaft main body.
シャフト本体の外周に設ける導電性弾性層は、シリコーンゴム、アクリロニトリルブタジエンゴム、ウレタンゴム、エチレンプロピレンゴム等のゴム材料をベースとし、これに導電性を付与するためにカーボンブラックや金属粉等の導電物質を配合した導電性ゴム材料で形成することができる。導電性弾性層は、導電性ゴム材料をシャフト本体の外周に被覆した後、常法により砥石等で研磨・研削することによって形成される。あるいは、導電性弾性材料で形成されたチューブ体をシャフト本体の外周に接着させ、チューブ体を常法により研磨・研削することによっても導電性弾性層を形成することができる。いずれの場合にも、研磨は、本体の外周に設けられた導電性弾性材料を有するシャフトを両ジャーナル部で支持し、シャフトを回転させながら行う。最終の導電性弾性層(研磨後)の厚さは、研磨精度の観点から、0.2mm以上であることが好ましい。研磨後の導電性弾性層の厚さは、通常10mm以下である。 The conductive elastic layer provided on the outer periphery of the shaft body is based on a rubber material such as silicone rubber, acrylonitrile butadiene rubber, urethane rubber, ethylene propylene rubber, etc. In order to impart conductivity to this, conductive material such as carbon black or metal powder is used. It can be formed of a conductive rubber material containing a substance. The conductive elastic layer is formed by coating a conductive rubber material on the outer periphery of the shaft body and then polishing and grinding with a grindstone or the like by a conventional method. Alternatively, the conductive elastic layer can also be formed by adhering a tube body made of a conductive elastic material to the outer periphery of the shaft body and polishing and grinding the tube body by a conventional method. In either case, the polishing is performed while supporting the shaft having the conductive elastic material provided on the outer periphery of the main body with both journal portions and rotating the shaft. The thickness of the final conductive elastic layer (after polishing) is preferably 0.2 mm or more from the viewpoint of polishing accuracy. The thickness of the conductive elastic layer after polishing is usually 10 mm or less.
ところで、導電性弾性層が予め硬化させた導電性ゴムチューブからなる場合、樹脂系シャフトの外径に対し、導電性ゴムチューブの内径が過大であると、後に行われるチューブの研磨の際に、樹脂系シャフトに対しチューブの滑りが発生し、チューブの外径寸法精度の低下は、振れ精度の低下を招く一方、硬化導電性ゴムチューブの内径が過小であると、シャフトをチューブに圧入する際に発生する歪がチューブ中に残留し、チューブ外径振れ精度の低下を招く。この問題を解消するために、樹脂系シャフトの外径dsに対する硬化導電性ゴムチューブの内径deの比de/dsを0.75〜0.97に設定し、および/または樹脂系シャフトの外径dsと硬化導電性ゴムチューブの内径deとの差ds−deを0.3mm以上、2.5mm以下に設定することが好ましい。 By the way, when the conductive elastic layer is made of a conductive rubber tube cured in advance, if the inner diameter of the conductive rubber tube is excessive with respect to the outer diameter of the resin-based shaft, when the tube is polished later, The tube slips on the resin shaft, and the decrease in dimensional accuracy of the tube causes a decrease in runout accuracy. On the other hand, if the inside diameter of the cured conductive rubber tube is too small, the shaft is pressed into the tube. The distortion generated in the tube remains in the tube, causing a decrease in the accuracy of tube outer diameter deflection. In order to solve this problem, the ratio de / ds of the inner diameter de of the cured conductive rubber tube to the outer diameter ds of the resin-based shaft is set to 0.75 to 0.97 and / or the outer diameter of the resin-based shaft. The difference ds−de between ds and the inner diameter de of the cured conductive rubber tube is preferably set to 0.3 mm or more and 2.5 mm or less.
このような樹脂系シャフトの外径dsとチューブの内径deとの関係を有することにより、硬化チューブの研磨の際に、樹脂系シャフトに対しチューブの滑りが発生せず、またシャフトをチューブに圧入する際に発生する歪がチューブ中に残留することがなく、寸法精度に優れた作像ローラが得られる。比de/dsは、0.8〜0.95であることが好ましい。また、差ds−deは、0.5〜2.5mmであることが好ましい。 By having such a relationship between the outer diameter ds of the resin-based shaft and the inner diameter de of the tube, the tube does not slip with respect to the resin-based shaft when the cured tube is polished, and the shaft is press-fitted into the tube. Thus, the image forming roller having excellent dimensional accuracy is obtained without causing distortion generated in the tube to remain in the tube. The ratio de / ds is preferably 0.8 to 0.95. The difference ds-de is preferably 0.5 to 2.5 mm.
導電性ゴムチューブは、シリコーンゴム、アクリロニトリルブタジエンゴム、ウレタンゴム、エチレンプロピレンゴム等のゴム材料をベースとし、これに導電性を付与するためにカーボンブラックや金属粉等の導電物質を配合した導電性ゴム材料で形成することができる。チューブは、未硬化の導電性ゴム材料をチューブ状に押出し、これを硬化させることにより形成できる。ここで、チューブは、その構成材料により、一次硬化のみで十分な場合と、一次硬化と二次硬化を行う方が好ましい場合がある。例えば、アクリロニトリルブタジエンゴム、ウレタンゴムは、80℃〜180℃で5分〜24時間で硬化させる一次硬化のみで十分である。他方、シリコーンゴムは、100℃〜400℃で1分〜10時間の条件で一次硬化を行った後、150℃〜250℃で1時間〜24時間の条件で二次硬化を行うことが好ましい。また、エチレンプロピレンゴムは、80℃〜180℃で5分〜24時間の条件で一次硬化を行った後、70℃〜150℃で1時間〜6時間の条件で二次硬化を行うことが好ましい。 Conductive rubber tube is based on rubber materials such as silicone rubber, acrylonitrile butadiene rubber, urethane rubber, ethylene propylene rubber, etc., and it is a conductive material that contains conductive materials such as carbon black and metal powder to give it conductivity. It can be formed of a rubber material. The tube can be formed by extruding an uncured conductive rubber material into a tube shape and curing it. Here, depending on the material of the tube, there may be a case where only primary curing is sufficient, and it is preferable to perform primary curing and secondary curing. For example, for acrylonitrile butadiene rubber and urethane rubber, it is sufficient only to perform primary curing at 80 ° C. to 180 ° C. for 5 minutes to 24 hours. On the other hand, the silicone rubber is preferably subjected to primary curing at 100 ° C. to 400 ° C. for 1 minute to 10 hours and then secondary curing at 150 ° C. to 250 ° C. for 1 hour to 24 hours. The ethylene propylene rubber is preferably subjected to primary curing at 80 ° C. to 180 ° C. for 5 minutes to 24 hours and then secondary curing at 70 ° C. to 150 ° C. for 1 hour to 6 hours. .
こうして得られた硬化導電性ゴムチューブを圧縮空気で拡径しながら、これに樹脂系シャフトを圧入する。その後、硬化導電性ゴムチューブ(導電性弾性層)を常法により砥石等で研磨・研削する。最終の導電性弾性層(研磨後)の厚さは、研磨精度の観点から、0.2mm以上、10mm以下であることが好ましい。樹脂系シャフトの外周とチューブの内周との間に接着剤、プライマー等を設けることは不要であり、樹脂系シャフトの外周とチューブの内周とを直接接触させることができる。 While expanding the diameter of the cured conductive rubber tube thus obtained with compressed air, a resin-based shaft is pressed into the tube. Thereafter, the cured conductive rubber tube (conductive elastic layer) is polished and ground with a grindstone or the like by a conventional method. The thickness of the final conductive elastic layer (after polishing) is preferably 0.2 mm or more and 10 mm or less from the viewpoint of polishing accuracy. It is not necessary to provide an adhesive, a primer, or the like between the outer periphery of the resin shaft and the inner periphery of the tube, and the outer periphery of the resin shaft and the inner periphery of the tube can be brought into direct contact.
なお、予め硬化させた導電性ゴムチューブは、ガラス転移点が100℃以下の樹脂系シャフトに適用することが特に有利である。このように低いガラス転移点を有する樹脂系シャフトは、上記一次硬化、二次硬化が行われるような高温で特に変形しやすいからである。特に本発明の樹脂系シャフトは、そのガラス転移点より+45℃を超える温度で加熱されると、変形が有意に生じやすい。 Note that it is particularly advantageous to apply the precured conductive rubber tube to a resin shaft having a glass transition point of 100 ° C. or less. This is because the resin shaft having such a low glass transition point is particularly easily deformed at a high temperature at which the primary curing and the secondary curing are performed. In particular, when the resin-based shaft of the present invention is heated at a temperature exceeding + 45 ° C. from its glass transition point, deformation is likely to occur significantly.
本発明の作像ローラにおいて、導電性弾性層の外周面には、弾性層の汚染の防止、耐摩耗性の向上、トナーに対する帯電性の最適化等を目的として、樹脂被覆層が設けられている。本発明において、この樹脂被覆層は、紫外線硬化樹脂または電子線硬化樹脂を含む。そのような紫外線または電子線硬化樹脂は、ポリエステルアクリレート、フッ素アクリレート、エポキシアクリレート、ウレタンアクリレート、シリコーンアクリレート等のアクリレートモノマーを紫外線または電子線により硬化させることにより得られる。より具体的には、これらアクリレートモノマーにベンゾイルエーテル系、チオオキサン系、ベンゾフェノン系等の光開始剤を配合した紫外線または電子線硬化性組成物を導電性弾性層の外周面に塗布し、紫外線または電子線を照射して硬化樹脂被覆層を形成する。紫外線または電子線硬化性組成物に配合する光開始剤の量は、アクリレートモノマー100質量部当たり、通常、0.1〜10質量部である。紫外線または電子線硬化性組成物には、光開始剤による硬化反応を促進させるために、重合促進剤を配合することができる。重合促進剤としては、第3級アミン系、アルキルホスフィン系、チオエーテル系等の重合促進剤を用いることができる。重合促進剤の配合量は、アクリレートモノマー100質量部当たり、通常、0.01〜10質量部である。さらに、紫外線または電子線硬化性組成物には、反応性希釈剤を配合することができる。反応性希釈剤は、紫外線または電子線硬化性組成物の粘度調整に用いられ、また反応性であることから硬化性組成物の硬化物(樹脂)中に取り込まれるため、非反応性希釈剤のように除去のために熱を掛ける必要はない。反応性希釈剤としては、例えば、アミノ酸または水酸基を含む化合物にアクリル酸をアミド化反応またはエステル化反応により結合させた単官能性、2官能性、多官能性の重合性化合物を例示することができる。より具体的には、ブタンジオール、ジエチレングリコール、ポリエチレングリコール、ネオペンチルグリコールのジアクリレートである。紫外線または電子線硬化性組成物に配合する反応性希釈剤の量は、アクリレートモノマー100質量部当たり、通常、10〜200質量部である。 In the image forming roller of the present invention, a resin coating layer is provided on the outer peripheral surface of the conductive elastic layer for the purpose of preventing contamination of the elastic layer, improving wear resistance, and optimizing the chargeability with respect to the toner. Yes. In the present invention, the resin coating layer contains an ultraviolet curable resin or an electron beam curable resin. Such an ultraviolet or electron beam curable resin can be obtained by curing an acrylate monomer such as polyester acrylate, fluorine acrylate, epoxy acrylate, urethane acrylate, or silicone acrylate with ultraviolet rays or an electron beam. More specifically, an ultraviolet ray or electron beam curable composition in which a photoinitiator such as benzoyl ether type, thiooxane type, or benzophenone type is blended with these acrylate monomers is applied to the outer peripheral surface of the conductive elastic layer, and ultraviolet rays or electrons are applied. A cured resin coating layer is formed by irradiating a line. The quantity of the photoinitiator mix | blended with a ultraviolet-ray or an electron beam curable composition is 0.1-10 mass parts normally per 100 mass parts of acrylate monomers. A polymerization accelerator can be blended with the ultraviolet ray or electron beam curable composition in order to accelerate the curing reaction by the photoinitiator. As the polymerization accelerator, a tertiary amine, alkylphosphine, thioether, or other polymerization accelerator can be used. The compounding quantity of a polymerization accelerator is 0.01-10 mass parts normally per 100 mass parts of acrylate monomers. Furthermore, a reactive diluent can be mix | blended with an ultraviolet-ray or an electron beam curable composition. The reactive diluent is used to adjust the viscosity of the ultraviolet ray or electron beam curable composition, and since it is reactive, it is incorporated into the cured product (resin) of the curable composition. Thus, it is not necessary to apply heat for removal. Examples of the reactive diluent include a monofunctional, difunctional and polyfunctional polymerizable compound in which acrylic acid is bonded to a compound containing an amino acid or a hydroxyl group by an amidation reaction or an esterification reaction. it can. More specifically, it is a diacrylate of butanediol, diethylene glycol, polyethylene glycol, or neopentyl glycol. The amount of the reactive diluent added to the ultraviolet ray or electron beam curable composition is usually 10 to 200 parts by mass per 100 parts by mass of the acrylate monomer.
樹脂被覆層の厚さは、通常、5〜100μmである。厚さが5μm未満では、耐久性に劣る場合があり、また厚さが100μmを超えると、その表面が硬くなりすぎ、トナーや感光体表面に対しダメージを与えるおそれがある。 The thickness of the resin coating layer is usually 5 to 100 μm. If the thickness is less than 5 μm, the durability may be inferior, and if the thickness exceeds 100 μm, the surface becomes too hard and the toner or the photoreceptor surface may be damaged.
本発明により、樹脂被覆層を紫外線硬化樹脂または電子線硬化樹脂で構成することにより、樹脂系シャフトは、高温(ガラス転移点より+45℃を超える温度)に供されることがなく、その熱による変形が防止される。 According to the present invention, by constituting the resin coating layer with an ultraviolet curable resin or an electron beam curable resin, the resin-based shaft is not subjected to a high temperature (a temperature exceeding + 45 ° C. from the glass transition point), and depends on the heat. Deformation is prevented.
本発明の作像ローラは、いずれも、現像ローラのほか、転写ローラ、トナー供給ローラ、クリーニングローラ等として提供され得る。 Any of the image forming rollers of the present invention can be provided as a transfer roller, a toner supply roller, a cleaning roller, etc. in addition to a developing roller.
以下、本発明の実施例を比較例とともに説明するが、本発明はそれらの例により限定されるものではない。 Examples of the present invention will be described below together with comparative examples, but the present invention is not limited to these examples.
実施例1〜10
芳香族ポリアミドとして三菱エンジニアリングプラスチックス社製ポリアミドMXD6を90質量部、脂肪族ポリアミドとして三菱エンジニアリングプラスチックス社製ノバミッド(登録商標)1007Jを10質量部、ガラス繊維として旭ファイバーグラス社製CS03−JAFT2を100質量部、カーボンブラックとして三菱化学社製#3050Bを12質量部配合した組成物を用い、直径10mm、面長(ゴム加工部)235mmのシャフトを射出成形し、ジャーナル部を切削加工で仕上げ、ブラザー工業社製プリンターHL−1850用現像ローラとして用いられる樹脂系シャフトを得た。樹脂系シャフトには破損は全くなかった。
Examples 1-10
90 parts by mass of polyamide MXD6 manufactured by Mitsubishi Engineering Plastics as aromatic polyamide, 10 parts by mass of Novamid (registered trademark) 1007J manufactured by Mitsubishi Engineering Plastics as aliphatic polyamide, and CS03-JAFT2 manufactured by Asahi Fiber Glass Co., Ltd. as glass fiber Using a composition containing 100 parts by mass, 12 parts by mass of Mitsubishi Chemical Corporation # 3050B as carbon black, a shaft having a diameter of 10 mm and a surface length (rubber processed part) of 235 mm is injection-molded, and the journal part is finished by cutting. A resin shaft used as a developing roller for a printer HL-1850 manufactured by Brother Industries, Ltd. was obtained. The resin shaft was not damaged at all.
得られた各シャフトの曲げ弾性率、曲げ強度、ガラス転移点、比重、表面抵抗を測定した。曲げ弾性率および曲げ強度は、東洋精機製作所社製ストログラフV10−Cにより、ガラス転移点は、島津製作所社製示差熱分析装置DSC−60により、比重は、アルファミラージュ社製電子比重計MD−200Sにより、体積抵抗率は、アドバンテスト社製抵抗計R8340により、それぞれ測定した。なお、ガラス転移点は、樹脂シャフトを5℃/分の加熱速度で加熱することによって測定した。曲げ弾性率は18GPaであり、曲げ強度は340MPaであり、ガラス転移点は78℃であり、比重は1.5であり、体積抵抗率は3×102であった。 The bending elastic modulus, bending strength, glass transition point, specific gravity, and surface resistance of each obtained shaft were measured. The flexural modulus and flexural strength were measured with a strograph V10-C manufactured by Toyo Seiki Seisakusho, the glass transition point was measured with a differential thermal analyzer DSC-60 manufactured by Shimadzu, and the specific gravity was an electronic hydrometer MD- manufactured by Alpha Mirage. With 200S, the volume resistivity was measured with a resistance meter R8340 manufactured by Advantest Corporation. The glass transition point was measured by heating the resin shaft at a heating rate of 5 ° C./min. The bending elastic modulus was 18 GPa, the bending strength was 340 MPa, the glass transition point was 78 ° C., the specific gravity was 1.5, and the volume resistivity was 3 × 10 2 .
他方、カーボンブラックが配合された未硬化シリコーンゴム材料(東レ・ダウコーニング社製DY32−4036)をチューブ状に押出し成形し、400℃で2分間硬化(一次硬化)させた後、所定の長さに切断し、200℃で4時間硬化(二次硬化)させて、内径deが7.5〜9.7mmで外径が20mmのチューブを得た。 On the other hand, an uncured silicone rubber material (DY32-4036 manufactured by Toray Dow Corning Co., Ltd.) containing carbon black is extruded into a tube shape, cured at 400 ° C. for 2 minutes (primary curing), and then a predetermined length. And cured at 200 ° C. for 4 hours (secondary curing) to obtain a tube having an inner diameter de of 7.5 to 9.7 mm and an outer diameter of 20 mm.
各チューブを圧縮空気で拡径しながら、これに上記樹脂系シャフトを圧入した後、表面を研磨し、外径が20mmのローラを作製した。なお、導電性シリコーンゴムチューブの体積抵抗率は106Ω・cmであり、JIS A硬度は45゜であった。 While expanding the diameter of each tube with compressed air, the resin-based shaft was press-fitted into the tube, and then the surface was polished to produce a roller having an outer diameter of 20 mm. The volume resistivity of the conductive silicone rubber tube was 10 6 Ω · cm, and the JIS A hardness was 45 °.
さらに、こうして得られたローラのいくつかについて振れを常法により測定した。すなわち、各ローラをジャーナル部で支持し、シャフトを回転させたときのシャフトの長手方向3箇所でのシャフトの変位の最大値と最小値を東京光電子工業製レーザ側長機RSV15100を用いて光学的に測定し、その差をシャフトの振れとして求めた。結果を下記表1に、「振れ(樹脂被覆層形成前)」として示す。 Further, the runout of some of the rollers thus obtained was measured by a conventional method. That is, the maximum value and the minimum value of the shaft displacement at three locations in the longitudinal direction of the shaft when each roller is supported by the journal portion and the shaft is rotated are optically measured using a laser-side long machine RSV15100 manufactured by Tokyo Koden Kogyo. The difference was determined as the shaft runout. The results are shown in the following Table 1 as “runout (before forming the resin coating layer)”.
次に、各ローラの導電性シリコーンゴムチューブ表面に対し10秒間のプラズマ処理(キーエンス社製プラズマ処理器ST−7000)を行った後、下記組成の紫外線硬化性樹脂組成物または電子線硬化性樹脂組成物を浸漬塗布し、紫外線(照射装置:アイグラフィックス社製EXH880;露光量:400mJ/cm2)または電子線(照射装置:岩崎電気社製LB−HP01;吸収線量:40KGy)を25℃で照射して硬化させ、それぞれ厚さ10μmの樹脂被覆層を形成し、作像ローラを得た。 Next, after conducting plasma treatment for 10 seconds on the surface of the conductive silicone rubber tube of each roller (Plasma processor ST-7000 manufactured by Keyence Corporation), an ultraviolet curable resin composition or an electron beam curable resin having the following composition: The composition was applied by dip coating, and ultraviolet rays (irradiation device: EXH880 manufactured by Eye Graphics Co., Ltd .; exposure amount: 400 mJ / cm 2 ) or electron beam (irradiation device: LB-HP01 manufactured by Iwasaki Electric Co., Ltd .; absorbed dose: 40 KGy) at 25 ° C. And cured by forming a resin coating layer having a thickness of 10 μm, respectively, to obtain an image forming roller.
<紫外線硬化性樹脂組成物>
モノマー:新中村化学社製ウレタンアクリレート(UAシリーズ)100質量部
反応性希釈剤:ジエチレングリコールジアクリレート30質量部
光開始剤:2−ヒドロキシ−4−n−オクチルオキシベンゾフェノン5質量部
<電子線硬化性樹脂組成物>
モノマー:新中村化学社製ウレタンアクリレート(UAシリーズ)100質量部
光開始剤:2−ヒドロキシ−4−n−オクチルオキシベンゾフェノン5質量部。
<Ultraviolet curable resin composition>
Monomer: 100 parts by mass of urethane acrylate (UA series) manufactured by Shin-Nakamura Chemical Co., Ltd. Reactive diluent: 30 parts by mass of diethylene glycol diacrylate Photoinitiator: 5 parts by mass of 2-hydroxy-4-n-octyloxybenzophenone <Electron beam curability Resin composition>
Monomer: 100 parts by mass of urethane acrylate (UA series) manufactured by Shin-Nakamura Chemical Co., Ltd. Photoinitiator: 5 parts by mass of 2-hydroxy-4-n-octyloxybenzophenone.
こうして得られた作像ローラのいくつかについて、上記と同様に振れを測定した。結果を表1に、「振れ(樹脂被覆層形成後)」として示す。 For some of the image forming rollers thus obtained, the shake was measured in the same manner as described above. The results are shown in Table 1 as “runout (after forming the resin coating layer)”.
比較例1〜10
フッ素含有ポリオール(ダイキン工業社製ゼッフル)100質量部と導電性カーボンブラック(キャボット社製)5質量部に酢酸ブチル300質量部を加え、分散機を用いて分散させた。この分散物に揮発性シリコーン油(信越化学工業社製KF96L)5質量部を加え、攪拌し主剤とした。この主剤に硬化剤としてウレタン変性ヘキサメチレンジイソシアネート(旭化成工業社製デュラネート)を主剤中のヒドロキシル基の当量と、硬化剤中のイソシアネート基の当量とが1:1となるように配合してコーティング材を調製した。このコーティング材を実施例1〜5で作製したローラ(樹脂被覆層形成前のもの)の導電性シリコーンゴムチューブ表面に厚さが10μmとなるようにスプレー塗装し、風乾した後、160℃で40分加熱して微小多孔質被覆層を形成し、現像ローラを得た。この現像ローラの振れを上記と同様に測定した。結果を表2に示す。
Comparative Examples 1-10
300 parts by mass of butyl acetate was added to 100 parts by mass of fluorine-containing polyol (Daikin Kogyo Zeffle) and 5 parts by mass of conductive carbon black (Cabot), and the mixture was dispersed using a disperser. To this dispersion, 5 parts by mass of volatile silicone oil (KF96L manufactured by Shin-Etsu Chemical Co., Ltd.) was added and stirred to obtain a main agent. A coating material in which urethane-modified hexamethylene diisocyanate (Duranate manufactured by Asahi Kasei Kogyo Co., Ltd.) as a curing agent is blended with this main agent so that the equivalent of the hydroxyl group in the main agent and the equivalent of the isocyanate group in the curing agent are 1: 1. Was prepared. This coating material was spray-coated on the surface of the conductive silicone rubber tube of the roller (before forming the resin coating layer) prepared in Examples 1 to 5 so as to have a thickness of 10 μm, air-dried, and then heated at 160 ° C. at 40 ° C. A minute porous coating layer was formed by heating for a minute to obtain a developing roller. The developing roller runout was measured in the same manner as described above. The results are shown in Table 2.
実施例1〜10および比較例1〜10で得た現像ローラをブラザー工業社製プリンターHL−1850に組み込み、10枚の通紙試験を行い、画像を以下の基準で評価した。 The developing rollers obtained in Examples 1 to 10 and Comparative Examples 1 to 10 were incorporated into a printer HL-1850 manufactured by Brother Industries, Ltd., 10 sheets were tested, and images were evaluated according to the following criteria.
<画像評価基準>
画像ムラなし…○
画像ムラややあるが実用上問題ない…△
画像ムラあり実用に耐えない…×
結果を、実施例1〜10については、表1に、比較例1〜10については表2に示す。
No image unevenness ... ○
There is some unevenness in the image, but there is no practical problem ... △
Uneven with image unevenness ... ×
The results are shown in Table 1 for Examples 1 to 10 and in Table 2 for Comparative Examples 1 to 10.
表1に示す結果から明らかなように、実施例1〜10の現像ローラは、樹脂被覆層を紫外線または電子線の照射により、[樹脂シャフトのガラス転移点+45℃]の温度未満の温度で硬化させているため、変形がなく、したがって振れも小さく、鮮明な画像を与える現像ローラを提供することができる。これに対し、表2に示すように、比較例1〜10の現像ローラは被覆層を形成するとき、160℃という高温を用いているため、変形が大きく、濃度ムラが生じている。 As is apparent from the results shown in Table 1, in the developing rollers of Examples 1 to 10, the resin coating layer was cured at a temperature lower than the temperature of [glass transition point of resin shaft + 45 ° C.] by irradiation with ultraviolet rays or electron beams. Therefore, it is possible to provide a developing roller that has no deformation and therefore has a small shake and gives a clear image. On the other hand, as shown in Table 2, since the developing rollers of Comparative Examples 1 to 10 use a high temperature of 160 ° C. when forming the coating layer, deformation is large and density unevenness occurs.
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Cited By (2)
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EP2159647A1 (en) * | 2008-08-27 | 2010-03-03 | Samsung Electronics Co., Ltd. | Roller, developing united and image forming apparatus having the same, and method of manufacturing roller |
WO2015030154A1 (en) * | 2013-08-30 | 2015-03-05 | 住友理工株式会社 | Conductive shaft, conductive roll for office automation device employing same, and method for fabrication of conductive shaft |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2001154478A (en) * | 1999-11-25 | 2001-06-08 | Bridgestone Corp | Nonmagnetic developing roller and image forming device using the same |
JP2003105197A (en) * | 2001-09-28 | 2003-04-09 | Mitsubishi Engineering Plastics Corp | Polyamide resin composition and molded product using the same |
JP2006023700A (en) * | 2004-06-09 | 2006-01-26 | Bridgestone Corp | Developing roller and image forming apparatus using same |
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JP2001154478A (en) * | 1999-11-25 | 2001-06-08 | Bridgestone Corp | Nonmagnetic developing roller and image forming device using the same |
JP2003105197A (en) * | 2001-09-28 | 2003-04-09 | Mitsubishi Engineering Plastics Corp | Polyamide resin composition and molded product using the same |
JP2006023700A (en) * | 2004-06-09 | 2006-01-26 | Bridgestone Corp | Developing roller and image forming apparatus using same |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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EP2159647A1 (en) * | 2008-08-27 | 2010-03-03 | Samsung Electronics Co., Ltd. | Roller, developing united and image forming apparatus having the same, and method of manufacturing roller |
US8280274B2 (en) | 2008-08-27 | 2012-10-02 | Samsung Electronics Co., Ltd. | Roller, developing unit and image forming apparatus having the same, and method of manufacturing roller |
WO2015030154A1 (en) * | 2013-08-30 | 2015-03-05 | 住友理工株式会社 | Conductive shaft, conductive roll for office automation device employing same, and method for fabrication of conductive shaft |
JP5853124B2 (en) * | 2013-08-30 | 2016-02-09 | 住友理工株式会社 | Conductive shaft, conductive roll for OA equipment using the same, and method for producing conductive shaft |
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