JPH0422979A - Developer carrying member - Google Patents
Developer carrying memberInfo
- Publication number
- JPH0422979A JPH0422979A JP2128676A JP12867690A JPH0422979A JP H0422979 A JPH0422979 A JP H0422979A JP 2128676 A JP2128676 A JP 2128676A JP 12867690 A JP12867690 A JP 12867690A JP H0422979 A JPH0422979 A JP H0422979A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- developer carrier
- developer
- carrying member
- carrier
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 230000005684 electric field Effects 0.000 claims abstract description 23
- 239000004094 surface-active agent Substances 0.000 claims abstract description 21
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000011737 fluorine Substances 0.000 claims abstract description 19
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims description 22
- 239000002671 adjuvant Substances 0.000 claims description 2
- 239000004020 conductor Substances 0.000 abstract description 10
- 238000011161 development Methods 0.000 description 22
- 239000010410 layer Substances 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 239000003989 dielectric material Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 108091008695 photoreceptors Proteins 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 239000012752 auxiliary agent Substances 0.000 description 5
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229920000620 organic polymer Polymers 0.000 description 4
- -1 polyethylene, ethylene-vinyl acetate Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 240000000015 Iris germanica Species 0.000 description 2
- 235000002971 Iris x germanica Nutrition 0.000 description 2
- 229920006311 Urethane elastomer Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 235000019241 carbon black Nutrition 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 239000000696 magnetic material Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 238000001454 recorded image Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 229920006235 chlorinated polyethylene elastomer Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000010416 ion conductor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 239000006247 magnetic powder Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000006234 thermal black Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical compound O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Dry Development In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、回転駆動される現像剤担持体に、必要に応じ
て補助剤を外添した非磁性一成分系現像剤を供給し、該
現像剤担持体の表面に前記現像剤を担持して搬送し、潜
像担持体と前記現像剤担持体が互いに対向した現像領域
にて、該潜像担持体に形成された静電潜像を現像剤担持
体に担持された前記現像剤によって可視像化する画像形
成方法に用いる現像剤担持体に関するものである。Detailed Description of the Invention [Industrial Field of Application] The present invention supplies a non-magnetic one-component developer to which an adjuvant is externally added as necessary to a rotationally driven developer carrier. The developer is carried on the surface of a developer carrier, and the electrostatic latent image formed on the latent image carrier is transferred to a development area where the latent image carrier and the developer carrier face each other. The present invention relates to a developer carrier used in an image forming method in which an image is visualized by the developer carried on the developer carrier.
潜像担持体に静電潜像を形成し、これを現像剤によって
可視像化して記録画像を得る電子複写機。An electronic copying machine that forms an electrostatic latent image on a latent image carrier and visualizes this using a developer to obtain a recorded image.
プリンタ或いはファクシミリ等の画像形成装置では、粉
体状の現像剤を用いる乾式の現像装置が広く採用されて
いる。2. Description of the Related Art In image forming apparatuses such as printers and facsimiles, dry-type developing devices that use powdered developer are widely used.
かかる粉体状の現像剤としては、トナーとキャリアを有
する二成分系現像剤と、キャリアを含まない一成分系現
像剤とが公知であり、前者の二成分系現像剤を用いた二
成分現像方式は、比較的安定した良好な記録画像が得ら
れる反面、キャリアの劣化やトナーとキャリアの混合比
の変動が発生しやすく、装置の維持管理が煩雑で、装置
全体の構造が大型化しやすくなる欠点を有している。As such powder-like developers, two-component developers containing toner and carrier and one-component developers that do not contain carrier are known, and two-component developers using the former two-component developer are known. Although this method allows relatively stable and good recorded images to be obtained, carrier deterioration and toner-to-carrier mixing ratio fluctuations are likely to occur, the maintenance and management of the device is complicated, and the overall structure of the device tends to increase in size. It has its drawbacks.
このような観点から、上述の欠点を有しない−成分系現
像剤を用いた一成分現像方式が注目されている。−成分
系現像剤は、トナーのみから成るものと、これに必要に
応じて補助剤を外添しトナーと補助剤を混合したものと
がある。またトナーとしては、その各トナー粒子自体に
磁性粉を練り込んだ磁性トナーと、磁性体を含まない非
磁性トナーとがある。From this point of view, a one-component development system using a -component developer, which does not have the above-mentioned drawbacks, is attracting attention. - Component-based developers include those consisting only of toner and those consisting of a mixture of toner and auxiliary agent, with external addition of an auxiliary agent as required. Furthermore, toners include magnetic toners in which magnetic powder is kneaded into each toner particle itself, and non-magnetic toners that do not contain magnetic material.
ここで、磁性体は一般に不透明であるため、フルカラー
やマルチカラーを含めたカラー画像を磁性トナーによっ
て形成すると、現像された可視像が不鮮明となり、鮮や
かなカラー画像を得ることはできない。従って、特にカ
ラー現像に対しては、非磁性トナーを用いた一成分現像
方式を採用することが望ましい。Here, since magnetic materials are generally opaque, when a full-color or multi-color image is formed using magnetic toner, the developed visible image becomes unclear, making it impossible to obtain a vivid color image. Therefore, especially for color development, it is desirable to adopt a one-component development method using non-magnetic toner.
ところで、−成分現像方式を採用した現像装置において
は、−成分系現像剤を現像剤担持体に担持させて搬送し
、この現像剤担持体と潜像担持体とが互いに対向した現
像領域において、潜像担持体に形成された静電潜像を現
像剤によって可視像化しているが、所定濃度の高品質な
可視像を形成するには、充分に帯電した多量のトナーを
現像領域に搬送し、かかるトナーによって潜像を可視像
化する必要がある。By the way, in a developing device that employs a -component development method, a -component developer is carried on a developer carrier and transported, and in a development area where the developer carrier and the latent image carrier face each other, The electrostatic latent image formed on the latent image carrier is made into a visible image using a developer, but in order to form a high-quality visible image with a predetermined density, a large amount of sufficiently charged toner must be applied to the development area. It is necessary to convey the latent image and visualize the latent image using the toner.
磁性トナーを用いた場合には、現像剤担持体に内設した
磁石の磁力を利用して、該担持体にこの一成分系現像剤
を担持てきるので、上述の要求を比較的容易に満たすこ
とが可能である。When magnetic toner is used, the one-component developer can be carried on the developer carrier by using the magnetic force of a magnet installed inside the developer carrier, so the above requirements can be met relatively easily. Is possible.
ところが、非磁性の一成分系現像剤を用いたときは、こ
れを磁力によって現像剤担持体に担持させることはでき
ないため、上述の要求を満たすことは難しい。これに対
する対策も従来より各種提案されており1例えば特開昭
61−42672号公報には、現像剤担持体(現像ロー
ラ)の表面に誘電体(絶縁体)の層を積層形成し、これ
に対して、例えばスポンジローラから成る現像剤供給部
材を圧接させ、両者を互いに異極性に摩擦帯電させると
共に、この誘電体と逆極性に帯電させた非磁性トナーを
誘電体に静電的に付着させ、かかる−成分系現像剤を現
像領域に搬送する方法が提案されている。しかし、この
方法によっても、誘電体表面の近傍に形成される電界の
強さを充分に高めることができないため、現像ローラの
表面に多量のトナーを担持させることは難しく、現像領
域へ搬送できる現像剤量が不足し、高濃度の可視像を形
成することは困難である。However, when a non-magnetic one-component developer is used, it is difficult to satisfy the above requirements because it cannot be supported on a developer carrier by magnetic force. Various countermeasures have been proposed in the past.1 For example, in Japanese Patent Application Laid-Open No. 61-42672, a dielectric (insulator) layer is laminated on the surface of a developer carrier (developing roller). A developer supply member made of, for example, a sponge roller is brought into pressure contact with the dielectric material, and the two are frictionally charged to opposite polarities, and non-magnetic toner charged to the opposite polarity to the dielectric material is electrostatically attached to the dielectric material. A method of transporting such a -component developer to a development area has been proposed. However, even with this method, it is not possible to sufficiently increase the strength of the electric field formed near the dielectric surface, so it is difficult to carry a large amount of toner on the surface of the developing roller. Due to the insufficient amount of agent, it is difficult to form a high-density visible image.
また、現像ローラと現像剤供給部材の間に、非磁性トナ
ーが現像ローラ側へ静電的に移行する向きの電界を印加
する構成も公知であるが、このような構成を付加しても
、現像ローラへ充分な量のトナーを付着させることは難
しい。Furthermore, a configuration is also known in which an electric field is applied between the developing roller and the developer supply member in a direction in which the non-magnetic toner electrostatically moves toward the developing roller, but even if such a configuration is added, It is difficult to make a sufficient amount of toner adhere to the developing roller.
なお、トナー供給部材としては、102〜106Ω・a
mの導電性発泡体(特開昭60−229057号公報)
、スキン層付弾性体(特開昭60−229060号公報
)及びファーブラシ(特開昭61−42672号公報)
等を使用することが提案されており、また現像ローラと
しては。In addition, as a toner supply member, 102 to 106 Ω・a
m conductive foam (Japanese Unexamined Patent Publication No. 60-229057)
, elastic body with skin layer (Japanese Unexamined Patent Publication No. 60-229060) and fur brush (Japanese Unexamined Patent Publication No. 61-42672)
It has been proposed to use a roller, etc., and as a developing roller.
表面に凹凸を有する金属体(特開昭60−53976号
公報)、絶縁被覆ローラ一体(特開昭55−46768
号公報)中低抗体被覆ローラ(特開昭58−13278
号公報)及び絶縁体と導電面を持つ電極ローラ(特開昭
53−36245号公報)等が開示されている。Metal body with uneven surface (Japanese Unexamined Patent Publication No. 60-53976), integral insulated roller (Unexamined Japanese Patent Application No. 55-46768)
Publication) Medium and low antibody coated roller (Japanese Patent Application Laid-Open No. 58-13278
JP-A-53-36245) and an electrode roller having an insulator and a conductive surface (JP-A-53-36245).
また、非磁性−成分現像剤を用いる現像装置において、
特開昭60−229057号公報ではスポンジローラ、
特開昭62−229060号公報では弾性ローラ、特開
昭61−52663号公報ではファーブラシ等を用いて
、トナーと補給部材との摩擦帯電でトナーに電荷を付与
し、更に現像ローラとの接触においての摩擦により、現
像ローラヘトナーを静電的に付着させ、更にブレード等
の層厚規制部材を用いて。Furthermore, in a developing device using a non-magnetic component developer,
In Japanese Patent Application Laid-Open No. 60-229057, a sponge roller,
JP-A No. 62-229060 uses an elastic roller, and JP-A No. 61-52663 uses a fur brush or the like to apply an electric charge to the toner through frictional charging between the toner and a replenishing member, and furthermore, by contact with a developing roller. The toner is electrostatically adhered to the developing roller by friction, and a layer thickness regulating member such as a blade is further used.
トナー層を制御して感光体の潜像を現像する。現像ロー
ラの材料としては、絶縁性のもの、中抵抗のもの、積層
のものなど各種のものが用いられている。The toner layer is controlled to develop the latent image on the photoreceptor. Various materials are used for the developing roller, such as insulating materials, medium resistance materials, and laminated materials.
これらの引例で示されている方式によると、現像ローラ
へのトナー付着は、トナー補給部材と現像ローラとの摩
擦帯電によって行なわれるが、トナーの付着した部材で
摩擦するため、充分な帯電が得にくく、結果的にトナー
付着が不足してしまう。非磁性−成分現像方式での最適
付着量と帯電量について説明すると、次のようになる。According to the methods shown in these references, toner adhesion to the developing roller is achieved by frictional electrification between the toner replenishing member and the developing roller, but sufficient electrification cannot be achieved due to friction between the toner-attached member. This results in insufficient toner adhesion. The optimum adhesion amount and charge amount in the non-magnetic component development method will be explained as follows.
白黒用では、帯電量が重視され、それは一般的に10〜
20μC/gである。この値より小さいと、地汚れ、シ
ャープ性などの画質面で劣るものとなる。For black and white, emphasis is placed on the amount of charge, which is generally 10~
It is 20μC/g. If the value is smaller than this value, the image quality will be poor in terms of background stains, sharpness, etc.
また、付着量に関しては、現像ローラ上の付着量は0.
1−0.3mg/ci+”であるが、転写紙上には0.
4−0.5mg/c+o”が必要であり、現像ローラの
スピードを感光体のスピードの3〜4倍にすることによ
って、トナーの付着量をカバーしている。ただ、3〜4
倍の現像ローラの回転には、″トナー後端より”という
現象、すなわちベタ部を現像した場合、画像の後端部の
濃度が高くなるという現象が、発生するという問題があ
る。この現象を防ぐには、現像ローラのスピードを感光
体のスピードに近ずけることである。つまり、現像ロー
ラ上の付着量を多くして1回転数を小さくしなければな
らない。Regarding the amount of adhesion, the amount of adhesion on the developing roller is 0.
1-0.3mg/ci+", but 0.3mg/ci+" on the transfer paper.
4-0.5mg/c+o" is required, and the amount of toner adhesion is covered by increasing the speed of the developing roller to 3 to 4 times the speed of the photoreceptor.
The problem with rotating the developing roller twice as much is that a phenomenon of "toner from the trailing edge" occurs, that is, when a solid area is developed, the density at the trailing edge of the image becomes higher. To prevent this phenomenon, the speed of the developing roller should be made close to the speed of the photoreceptor. In other words, it is necessary to increase the amount of toner adhered to the developing roller and reduce the number of revolutions per rotation.
一方、カラートナーでは、その色特性は黒トナーに比べ
て着色度が小さく、また“トナー後端より″を改良しよ
うとすると、黒トナーに比べ更に多い0.8〜1.2m
g/cm2という現像ローラ上の付着量が必要になる。On the other hand, with color toner, the degree of coloring is smaller than that of black toner, and when trying to improve the "from the rear end of the toner", the color characteristic is 0.8 to 1.2 m, which is even more than that of black toner.
An amount of adhesion on the developing roller of g/cm2 is required.
また、帯電量に関しては、安定した画像を得るためには
、5〜20μC/g(好ましくは10〜15μC/g)
の値が望まれる。In addition, regarding the amount of charge, in order to obtain a stable image, 5 to 20 μC/g (preferably 10 to 15 μC/g)
A value of is desired.
これらの問題点を解消する方法として、本発明者らは、
先に「回転駐動される現像剤担持体に、必要に応じて補
助剤を外添した非磁性トナーより成る一成分系現像剤を
供給し、該担持体の表面に前記現像剤を担持して搬送し
、潜像担持体と前記現像剤担持体が互いに対向した現像
領域にて、該潜像担持体に形成された静電潜像を現像剤
担持体に担持された前記現像剤によって可視像化する現
像方法において、前記現像剤担持体の表面に選択的に電
荷を保持させることにより該担持体表面の近傍に多数の
微小閉窒界を形成し、この閉電界により帯電トナーを吸
引し、現像剤を現像剤担持体表面に付着させて担持し、
該担持現像剤によって静電潜像を可視像化する画像形成
方法」を提案した。As a method to solve these problems, the present inventors
First, a one-component developer consisting of a non-magnetic toner to which an auxiliary agent is externally added as necessary is supplied to a rotating and parked developer carrier, and the developer is carried on the surface of the carrier. In a developing area where the latent image carrier and the developer carrier face each other, the electrostatic latent image formed on the latent image carrier is transferred by the developer carried by the developer carrier. In the visualization development method, a large number of minute closed nitrogen fields are formed near the surface of the developer carrier by selectively holding charges on the surface of the developer carrier, and the charged toner is attracted by this closed electric field. and deposit and carry the developer on the surface of the developer carrier,
We proposed an image forming method in which an electrostatic latent image is visualized using the developer carried thereon.
かかる発明は、現像剤担持体の表面の近傍に多数の微小
閉窒界(マイクロフィールド)が形成されるので、その
電界強度を従来よりも著しく増大させることができ、充
分に帯電した多量の非磁性トナーを現像剤担持体に担持
して現像領域に搬送できるといった多くの利点を有する
ものである。In this invention, since a large number of micro-closing fields (micro-fields) are formed near the surface of the developer carrier, the electric field strength can be significantly increased compared to the conventional method, and a large amount of sufficiently charged non-nitride fields can be generated. This device has many advantages such as being able to carry magnetic toner on a developer carrier and transport it to a developing area.
ただ、前記のような現像剤担持体表面の近傍に多数のマ
イクロフィールドが形成される画像形成方法においても
、現像剤担持体には多くの部材、例えばトナー供給部材
、トナー層厚規制部材、(接触現像時には)感光体等が
当接されている。そのため、現像剤担持体の表面の摩擦
係数が大きいと、現像剤担持体の回転トルクが大きくな
り、振動の原因や強力なモーターが必要となる。その上
。However, even in the image forming method in which a large number of microfields are formed near the surface of the developer carrier as described above, there are many members on the developer carrier, such as a toner supply member, a toner layer thickness regulating member, (during contact development) a photoreceptor, etc. is in contact with the photoreceptor. Therefore, if the friction coefficient of the surface of the developer carrier is large, the rotational torque of the developer carrier becomes large, causing vibrations and requiring a powerful motor. On top of that.
現像剤担持体上のトナーが撹拌不足になり、現像剤担持
体表面にトナーが固着する、いわゆるフィルミング現象
が発生したり、あるいはトナーの帯電量が不足したりな
どするという問題点がある。There are problems such as insufficient agitation of the toner on the developer carrier, resulting in so-called filming phenomenon in which the toner sticks to the surface of the developer carrier, or an insufficient amount of charge on the toner.
従って、本発明の目的は、前記の画像形成方法において
、フィルミング発生やトナー帯電量不足という問題点を
解消する現像剤担持体を提供することにある。Therefore, it is an object of the present invention to provide a developer carrier that solves the problems of filming and insufficient toner charge in the image forming method described above.
本発明者らは、鋭意検討した結果、!像側担持体の少な
くとも表面又は表面近傍にフッ素系界面活性剤を含有し
た現像剤担持体が、上記目的に適合することを知見し、
本発明を完成するに至った。As a result of intensive study, the inventors found that! It has been found that a developer carrier containing a fluorine-based surfactant at least on the surface or near the surface of the image-side carrier is compatible with the above purpose,
The present invention has now been completed.
すなわち、本発明によれば、現像剤担持体の表面上に1
選択的に電荷を保持させることにより。That is, according to the present invention, 1
By selectively retaining charge.
現像剤担持体表面近傍に多数の微小閉窒界を形成し、こ
の現像剤担持体上に、必要に応して補助剤を外添したト
ナーよりなる非磁性一成分系現像剤を供給し、前記微小
閉窒界により前記現像剤を現像剤担持体表面に担持させ
、該担持現像剤によって静電潜像を可視像化する画像形
成方法に用いる現像剤担持体であって、少なくともその
表面又は表面近傍にフッ素系界面活性剤が含有されてい
るものであることを特徴とする現像剤担持体が提供され
る。Forming a large number of minute closed nitrogen fields near the surface of a developer carrier, and supplying a non-magnetic one-component developer made of toner to which an auxiliary agent is externally added as necessary onto the developer carrier; A developer carrier used in an image forming method in which the developer is supported on the surface of the developer carrier by the micro-nitriding field and an electrostatic latent image is visualized by the carried developer, the developer carrier comprising at least the surface of the developer carrier. Alternatively, there is provided a developer carrier characterized in that a fluorine-based surfactant is contained near the surface.
本発明の現像剤担持体を用いる画像形成方法は、現像剤
担持体表面の近傍に多数の微小閉窒界が形成されるので
、その電界強度を従来よりも著しく増大させることがで
きる上に、現像剤担持体表面又は表面近傍にフッ素系界
面活性剤が含有されることにより、現像剤担持体表面の
摩擦係数が低減し、その結果トナーフィルミングが発生
せず、充分に帯電した多量の非磁性トナーを現像剤担持
体に担持して現像領域に搬送できるものとなる。In the image forming method using the developer carrier of the present invention, a large number of micro-closing fields are formed near the surface of the developer carrier, so the electric field strength can be significantly increased compared to the conventional method, and By containing a fluorine-based surfactant on or near the surface of the developer carrier, the coefficient of friction on the surface of the developer carrier is reduced, and as a result, toner filming does not occur and a large amount of sufficiently charged particles The magnetic toner can be carried on the developer carrier and transported to the development area.
以下5かかる画像形成方法について説明する。Below, five such image forming methods will be explained.
第1図にこの画像形成方法の実施に有用な代表的な現像
装置の現像剤担持体部を中心とした概要を示す。第1図
において、トナータンク70に内蔵されているトナー6
0は、撹拌羽根(トナー供給補助部材)50によりトナ
ー供給部材(スポンジローラ又はファーブラシなど)4
0に強制的に寄せられ、トナー60はトナー供給部材4
0に供給される。一方、現像を終了した本発明の現像剤
担持体(現像ローラ)20は、矢印の方向に回転(例え
ば400rpm) シ、トナー供給部材40との接触部
に至る。トナー供給部材40は現像剤担持体20と逆方
向に回転(例えば300rp+m) L、現像剤担持体
20とトナー60に帯電を与え、現像剤担持体20上に
トナー60を付着させる。FIG. 1 shows an outline of a typical developing device useful for carrying out this image forming method, centering on the developer carrier section. In FIG. 1, toner 6 contained in a toner tank 70 is shown.
0 is a toner supply member (sponge roller, fur brush, etc.) 4 by a stirring blade (toner supply auxiliary member) 50.
0, the toner 60 is forcibly brought to the toner supply member 4
0. On the other hand, the developer carrier (developing roller) 20 of the present invention, which has completed the development, rotates in the direction of the arrow (for example, at 400 rpm) and reaches the contact portion with the toner supply member 40 . The toner supply member 40 rotates in the opposite direction to the developer carrier 20 (for example, 300 rpm+m) L, charges the developer carrier 20 and the toner 60, and causes the toner 60 to adhere onto the developer carrier 20.
更に現像剤担持体20は回転し、現像剤担持体20上の
付着トナーは、トナー層厚規制部材(弾性ブレード)3
0により、厚みを制御されながら帯電も安定化され、現
像域80に達する。現像域80において、接触又は非接
触現像により、潜像が現像される。Further, the developer carrier 20 rotates, and the toner adhering to the developer carrier 20 is removed by the toner layer thickness regulating member (elastic blade) 3.
0, the charging is stabilized while the thickness is controlled, and the developing area 80 is reached. In the development area 80, the latent image is developed by contact or non-contact development.
ここで必要に応じて、現像剤担持体20、トナー供給部
材40に直流、交流、直流重畳交流、パルスなどのバイ
アスなどを印加して、最適な画像を制御することができ
る。Here, if necessary, bias such as direct current, alternating current, direct current superimposed alternating current, pulse, etc. can be applied to the developer carrier 20 and the toner supply member 40 to control an optimal image.
次に、このタイプ(電極タイプ)の現像剤担持体20へ
のトナー付着のメカニズムについて説明する。Next, the mechanism of toner adhesion to this type (electrode type) developer carrier 20 will be explained.
現像剤担持体20の例としては、たとえば第2図に示さ
れるように、その表面に誘電体部と導電体部とが微小面
積で混在するように構成されている。As an example of the developer carrier 20, as shown in FIG. 2, the developer carrier 20 is configured such that a dielectric portion and a conductive portion coexist in a small area on its surface.
面積の大きさは、形状が円形であるとした場合。The size of the area is assuming that the shape is circular.
径が10〜500−の大きさの微小面積がランダムに又
はある規則にしたがって分散している8面積比としては
、導電部の面積が20〜60%の範囲が好ましい。The area ratio in which minute areas with diameters of 10 to 500 mm are distributed randomly or according to a certain rule is preferably in the range of 20 to 60% of the area of the conductive part.
トナー付着は次のようになる。まず、現像を終了した現
像剤担持体20は、矢印の方向に回転してトナー供給部
材40と接触する。ここで現像しなかった非画像部の残
トナーは、トナー供給部材40により機械的、電気的に
かきとられ、誘電体部は摩擦によって帯電する。このと
き前の現像による現像剤担持体20とトナーの電荷は、
摩擦により一定化され、初期化される。次に、供給部材
40によって運ばれたトナーは、摩擦により帯電し、現
像剤担持体20の誘電体部に静電的に付着する。このと
きの極性は、感光体電荷に対してトナーは逆極性にまた
現像剤担持体20の誘電体部は同極性となる。Toner adhesion is as follows. First, the developer carrier 20 that has completed development rotates in the direction of the arrow and comes into contact with the toner supply member 40 . The remaining toner in the non-image area that has not been developed is mechanically and electrically scraped off by the toner supply member 40, and the dielectric portion is charged by friction. At this time, the charges on the developer carrier 20 and toner due to the previous development are as follows:
It is stabilized and initialized by friction. Next, the toner carried by the supply member 40 is charged by friction and electrostatically adheres to the dielectric portion of the developer carrier 20 . At this time, the polarity of the toner is opposite to the charge on the photoreceptor, and the dielectric portion of the developer carrier 20 is of the same polarity.
このときの現像剤担持体20上の電界は、第2図に示さ
れるようにマイクロフィールド(閉電界)となり、電界
傾度の大きい電界となって、トナーを多層に付着させる
ことが可能となる。また、付着したトナーは閉電界とな
っているので、現像剤担持体20側に強く引かれ離れに
くい状態となる。At this time, the electric field on the developer carrier 20 becomes a microfield (closed electric field) as shown in FIG. 2, and becomes an electric field with a large electric field gradient, making it possible to adhere the toner in multiple layers. Further, since the adhered toner is in a closed electric field, it is strongly attracted to the developer carrier 20 side and becomes difficult to separate.
このトナー層は、更にトナー層厚規制部材30によりト
ナー層厚が制御され、現像域80に達する。The thickness of this toner layer is further controlled by a toner layer thickness regulating member 30, and the toner layer reaches the development area 80.
現像域80での現像剤担持体20と静電潜像担持体(感
光体)10間の電界は、電極効果が大きくなり、現像剤
担持体20上のトナーは静電潜像担持体10に付着し易
い電界となり、現像が行なわれる。The electric field between the developer carrier 20 and the electrostatic latent image carrier (photoreceptor) 10 in the development area 80 has a large electrode effect, and the toner on the developer carrier 20 is transferred to the electrostatic latent image carrier 10. The electric field becomes easy to adhere to, and development is performed.
次に、本発明の現像剤担持体について説明する。Next, the developer carrier of the present invention will be explained.
導電性材料としては、1012Ω・cm以下、好ましく
はlO8Ω・cm以下のものが使用できる。具体例とし
ては、AQ、 SO5,Fe、 Niなどの金属類、−
t! 5 ミックス類などの他に、有機ポリマー類に導
電性付与剤を添加したものが挙げられる。この場合、有
機ポリマー類としては次のものが挙げられる。As the conductive material, one having a resistance of 10 12 Ω·cm or less, preferably 1O 8 Ω·cm or less can be used. Specific examples include metals such as AQ, SO5, Fe, Ni, -
T! 5. In addition to mixes, examples include organic polymers to which a conductivity imparting agent is added. In this case, the organic polymers include the following.
ポリ塩化ビニル、ポリビニルブチラール、ポリビニルア
ルコール、ポリ塩化ビニリデン、ポリ酢酸ビニル、ポリ
ビニルホルマールなどのビニル系樹脂;ポリスチレン、
スチレン−アクリロニトリル共重合体、アクリロニトリ
ル−ブタジェン−スチレン共重合体などのポリスチレン
系樹脂;ポリエチレン、エチレン−酢酸ビニル共重合体
などのポリエチレン系樹脂;ポリメチルメタクリレート
、ポリメチルメタクリレート−スチレン共重合体などの
アクリル系樹脂;ポリアセタール、ポリアミド、セルロ
ース、ポリカーボネート、フェノキシ樹脂、ポリエステ
ル、フッ素樹脂、ポリウレタン、フエ/−ル樹脂、尿素
樹脂、メラミン樹脂、エポキシ樹脂、不飽和ポリエステ
ル樹脂、シリコーン樹脂等の樹脂材料;天然ゴム、イン
プレンゴム、ブタジェンゴム、スチレン−ブタジェンゴ
ム、ブチルゴム、エチレン−プロピレンゴム、クロロプ
レンゴム、塩素化ポリエチレンゴム、エピクロルヒドリ
ンゴム、ニトリルゴム、アクリルゴム、ウレタンゴム、
多硫化ゴム、シリコーンゴム、フッ素ゴム等のゴム材料
など。Vinyl resins such as polyvinyl chloride, polyvinyl butyral, polyvinyl alcohol, polyvinylidene chloride, polyvinyl acetate, and polyvinyl formal; polystyrene,
Polystyrene resins such as styrene-acrylonitrile copolymer, acrylonitrile-butadiene-styrene copolymer; polyethylene resins such as polyethylene, ethylene-vinyl acetate copolymer; polymethyl methacrylate, polymethyl methacrylate-styrene copolymer, etc. Acrylic resin; resin materials such as polyacetal, polyamide, cellulose, polycarbonate, phenoxy resin, polyester, fluororesin, polyurethane, phenylene resin, urea resin, melamine resin, epoxy resin, unsaturated polyester resin, silicone resin; natural Rubber, imprene rubber, butadiene rubber, styrene-butadiene rubber, butyl rubber, ethylene-propylene rubber, chloroprene rubber, chlorinated polyethylene rubber, epichlorohydrin rubber, nitrile rubber, acrylic rubber, urethane rubber,
Rubber materials such as polysulfide rubber, silicone rubber, fluororubber, etc.
また、導電性付与剤としては、Ni、Cuなどの金属粉
;ファーネスブラック、ランプブラック、サーマルブラ
ック、アセチレンブラック、チャンネルブラックなどの
カーボンブラック;酸化スズ、酸化亜鉛、酸化モリブデ
ン、酸化アンチモン、チタン酸カリなどの導電性酸化物
;酸化チタン、雲母上などにめっきを施した無電界めっ
き物;グラファイト、金属繊維、炭素繊維などの無機系
充填剤や界面活性剤などが挙げられる。In addition, conductivity imparting agents include metal powders such as Ni and Cu; carbon blacks such as furnace black, lamp black, thermal black, acetylene black, and channel black; tin oxide, zinc oxide, molybdenum oxide, antimony oxide, and titanic acid. Conductive oxides such as potash; electroless plated materials such as titanium oxide and mica; inorganic fillers such as graphite, metal fibers, and carbon fibers; surfactants; and the like.
なお、ポリエチレンオキサイドやポリシロキサンなどの
ポリマーマトリックスに金属イオンを配位させた有機イ
オン伝導体なども用いることができる。Note that an organic ion conductor in which metal ions are coordinated to a polymer matrix such as polyethylene oxide or polysiloxane can also be used.
一方、誘電体部に用いる材料は、絶縁性であれば、使用
可能であるが、1013Ω・011以上、特に10’1
Ω・cm以上のものが好ましい。その具体例としては、
導電性材料中で挙げた有機ポリマー類が挙げられる。On the other hand, the material used for the dielectric part can be used as long as it is insulating, but it should be 1013Ω・011 or more, especially 10'1
It is preferable to have a resistance of Ω·cm or more. As a specific example,
Examples include the organic polymers listed in the conductive materials.
本発明の現像剤担持体は、少なくともその表面又は表面
近傍にフッ素系界面活性剤を含有することを特徴とする
。この場合のフッ素系界面活性剤としては、フルオロア
ルキル基を含有するフッ素化合物であれば、いずれのも
のも使用できる。The developer carrier of the present invention is characterized in that it contains a fluorine-containing surfactant at least on its surface or near its surface. As the fluorine-based surfactant in this case, any fluorine compound containing a fluoroalkyl group can be used.
般には、ノニオン性、アニオン性、カチオン性。Generally nonionic, anionic, and cationic.
両性などがあるが、アニオン性のものが好ましい。Although there are amphoteric ones, anionic ones are preferable.
これらのフッ素系界面活性剤の具体例としては、ノニオ
ン系のものとして、例えばパーフルオロアルキル基親油
性基含有オリゴマー、パーフルオロアルキル基親水性基
含有オリゴマー、パーフルオロアルキルエチレンオキシ
ド付加物などが挙げられる。また、カチオン性のものと
しては、パーフルオロアルキル含有第4級アンモニウム
塩など。Specific examples of these fluorine-based surfactants include nonionic ones, such as perfluoroalkyl group-containing lipophilic group-containing oligomers, perfluoroalkyl group-containing hydrophilic group-containing oligomers, perfluoroalkyl ethylene oxide adducts, etc. . In addition, examples of cationic substances include perfluoroalkyl-containing quaternary ammonium salts.
アニオン性のものとしては、パーフルオロアルキルを含
有したスルホン酸、カルボン酸の一価金属塩やリン酸エ
ステルなど、両性のものとしてはパーフルオロアルキル
を含有したベタインなどが挙げられる。Examples of anionic compounds include sulfonic acids containing perfluoroalkyl, monovalent metal salts of carboxylic acids, and phosphate esters, and examples of amphoteric compounds include betaine containing perfluoroalkyl.
なお、このようなフッ素系界面活性剤の市販品としては
1例えばサーフロン(旭硝子社製)、メガファック(大
日本インキ化学社製)、エフトップ(旭硝子社製)、フ
タージェレト(ネオス社製)、ユニダイン(ダイキン工
業社製)等がある。Commercially available products of such fluorine-based surfactants include Surflon (manufactured by Asahi Glass Co., Ltd.), Megafac (manufactured by Dainippon Ink Chemical Co., Ltd.), FTOP (manufactured by Asahi Glass Co., Ltd.), Futtergelet (manufactured by Neos Co., Ltd.), Examples include Unidyne (manufactured by Daikin Industries).
これらは、用いる材料との相溶性等の点から適宜選択す
ることができる。また、各種界面活性剤との混合併用も
可能である。フッ素系界面活性剤の混入量は、用いる材
料の固形分100重量部に対して、0.1〜50重量部
が好ましい。より好ましくは0.5〜20重量部である
。0.1重量部未満では、摩擦係数低減の効果が充分現
われず、逆に50重量部を越えると、材料の機械的強度
の低下などが生じる6本発明の現像剤担持体を作製する
には、例えば。These can be appropriately selected from the viewpoint of compatibility with the materials used. It is also possible to mix and use various surfactants. The amount of the fluorosurfactant mixed is preferably 0.1 to 50 parts by weight based on 100 parts by weight of the solid content of the material used. More preferably, it is 0.5 to 20 parts by weight. If it is less than 0.1 part by weight, the effect of reducing the coefficient of friction will not be sufficiently exhibited, and if it exceeds 50 parts by weight, the mechanical strength of the material will decrease. 6. How to make the developer carrier of the present invention ,for example.
(i)まず、金属ローラの表面にフッ素系界面活性剤を
添加した導電性材料を、射出成型、押し出し成型、プレ
ス成型、スプレーコーティング、ディッピング等の通常
の成型方法により、層成型し。(i) First, a conductive material containing a fluorine-based surfactant is layer-molded on the surface of a metal roller using a conventional molding method such as injection molding, extrusion molding, press molding, spray coating, or dipping.
(ii)表面にアヤメローレット加工等により溝加工を
施しくこの場合、■溝は0.1〜0 、5eunピツチ
とし。(ii) The surface is grooved by fleur-de-lis knurling, etc. In this case, the grooves are 0.1-0.5 eun pitch.
ローラ長手方向に対して、約45°の角度に加工する)
〔参照;第3図(a)〕、(iii)次に溝加工した金
属表面に、予めフッ素系添加剤を含有した誘電材料を、
スプレー、ディッピングなどの方法によりコーティング
し、所定の硬化若しくは乾燥温度/時間により成型しく
塗布厚みは溝が完全に埋まる状態にする)〔参照;第3
図(b))、 (iv)続いてローラの表面を切削又は
研磨加工により導電面と誘電面が微小面積で混在するよ
うに削り、導電部面積が20〜60%になるように削る
〔参照;第3図(C)〕という方法が採用される。Processed at an angle of approximately 45° to the longitudinal direction of the roller)
[See Figure 3(a)], (iii) Next, a dielectric material containing a fluorine-based additive in advance is applied to the grooved metal surface.
It is coated by spraying, dipping, etc., and molded at a predetermined curing or drying temperature/time, and the coating thickness is adjusted so that the grooves are completely filled.) [Refer to Part 3]
Figure (b)), (iv) Next, the surface of the roller is cut or polished so that the conductive surface and dielectric surface are mixed in a small area, and the area of the conductive part is reduced to 20 to 60% [see The method shown in FIG. 3(C) is adopted.
本発明の現像剤担持体の表面の代表的な構成例は、第4
図(a)−(d)で示される。第4図(a)及び(b)
で示される構成においては、導電性及び誘電性材料にフ
ッ素系界面活性剤が添加可能な材料1例えば有機ポリマ
ー類などが用いられた場合、直接両者にフッ素系界面活
性剤を添加して、摩擦係数を低減することができる。第
4図(c)で示されるように、誘電体部の静電容量の差
により電界傾度を形成した例では、誘電体にのみフッ素
系界面活性剤を添加すれば良い。また、第4図(d)で
示さるように、金属材料など界面活性剤の添加が不可能
な材料を用いた場合には、表面層としてフッ素系界面活
性剤を含有する層を設置すれば良い。A typical configuration example of the surface of the developer carrier of the present invention is as follows:
Shown in Figures (a)-(d). Figure 4 (a) and (b)
In the configuration shown in , when a material 1 to which a fluorine-based surfactant can be added to the conductive and dielectric materials is used, such as organic polymers, the fluorine-based surfactant is directly added to both to improve friction. The coefficient can be reduced. As shown in FIG. 4(c), in an example in which an electric field gradient is formed by a difference in capacitance between dielectric parts, it is sufficient to add a fluorine-based surfactant only to the dielectric. In addition, as shown in Figure 4(d), when using materials such as metal materials to which it is impossible to add a surfactant, a layer containing a fluorine-based surfactant may be installed as a surface layer. good.
(実施例〕
以下、実施例により本発明を更に詳細に説明する。なお
1部は重量部を表わす。(Example) Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that 1 part represents part by weight.
実施例
導電性材料
Sn系触媒(商品名Cat、55:三洋化成工業三層化
成工業社製ルエチルケトン
ノニオン性フッ素系界面活性剤
300部
1部
(商品名サーフロンS−382;旭硝子社製)誘電部材
料
上記導電性材料の処方よりカーボンブラック繊維を除い
たもの。Examples Conductive material Sn-based catalyst (trade name Cat, 55: manufactured by Sanyo Kasei Chemical Industry Co., Ltd. 300 parts of ethyl ketone nonionic fluorine-based surfactant 1 part (trade name Surflon S-382; manufactured by Asahi Glass Co., Ltd.) Dielectric material: Carbon black fibers are removed from the above conductive material formulation.
上記処方の材料を用い、次の要領により現像剤担持体(
現像ローラ)を作製した。Using the materials of the above formulation, the developer carrier (
A developing roller) was manufactured.
(i)SUS製ローラに、スプレーコーティングにより
、上記導電性材料をコーティングし、100℃71時間
の条件で硬化させた後、研磨を施し、膜厚50趨の導電
層を得た。(i) A SUS roller was coated with the above conductive material by spray coating, cured at 100° C. for 71 hours, and then polished to obtain a conductive layer with a thickness of 50 mm.
(ii)ローラ表面にアヤメローレット加工により、■
溝を設けた。■溝は0.2Illピツチとし、ローラ長
手方向に対して約45度に加工した。(ii) With fleur-de-lis knurling on the roller surface, ■
A groove was provided. (2) The grooves had a pitch of 0.2Ill and were machined at approximately 45 degrees to the longitudinal direction of the roller.
(ni)V溝加工したローラ表面に上記誘電部材料を、
(i)と同様の方法で成型した。塗布厚みは溝が完全に
埋まる状態とした。(ni) Apply the above dielectric material to the V-grooved roller surface,
It was molded in the same manner as (i). The coating thickness was such that the grooves were completely filled.
(iv)ローラの表面を研磨し、導電面と誘電面が微小
面積で混在するようにして、導電部面積を50%とした
。(iv) The surface of the roller was polished so that a conductive surface and a dielectric surface coexisted in a small area, so that the conductive part area was 50%.
次の方法により、動摩擦係数及びトナーフィルミング試
験を行なった。Dynamic friction coefficient and toner filming tests were conducted using the following method.
動摩擦係数の測 法
導電材料、誘電材料を、PETシートにスプレーコーテ
ィングして、膜厚20A@のシートを得た。Measurement of Dynamic Friction Coefficient A conductive material and a dielectric material were spray coated onto a PET sheet to obtain a sheet with a film thickness of 20A@.
摩擦係数測定装置 : HEIDON14型表面性測定
機平面圧子: 30mm+ X 30mm圧子荷重:1
kg
圧子送り速度: 50mm/+win
動摩擦係数μ=W(ストレンゲージ値)/P(加圧力)
により、動摩擦係数を算出した。Friction coefficient measuring device: HEIDON 14 type surface property measuring device Plane indenter: 30mm+ x 30mm Indenter load: 1
kg Indenter feed speed: 50mm/+win Dynamic friction coefficient μ=W (strain gauge value)/P (pressing force)
The coefficient of dynamic friction was calculated.
トナーフィルミング
現像ローラを第1図に示される現像装置に装着し、10
0時間現像ローラの駆動試験を行なった後。Attach the toner filming developing roller to the developing device shown in FIG.
After conducting a 0-hour developing roller drive test.
ローラ表面のトナーをエアーにより吹き飛ばし、ローラ
表面をテープ転写し、トナーのフィルミング状態を目視
I察した。The toner on the roller surface was blown off with air, the roller surface was transferred to a tape, and the filming state of the toner was visually observed.
なお、上記現像装置において、トナー薄層化ブレードは
ウレタンゴム製のものを、トナー供給ローラは導電性ウ
レタンスポンジ製のものを、トナーは負帯電トナーを、
装填した。In the above developing device, the toner thinning blade is made of urethane rubber, the toner supply roller is made of conductive urethane sponge, and the toner is negatively charged toner.
Loaded.
比較例
実施例において、導電性材料及び誘電部材料中のフッ素
系界面活性剤を使用しなかった以外は、実施例と同様に
して現像ローラ及びシートを作製し、動摩擦係数の測定
及びトナーフィルミング試験を行なった。Comparative Example A developing roller and sheet were prepared in the same manner as in the example except that the fluorine-based surfactant in the conductive material and dielectric material was not used, and the measurement of the coefficient of dynamic friction and toner filming were carried out in the same manner as in the example. I conducted a test.
評価 動摩擦係数の測定結果を第1表に示す。evaluation Table 1 shows the measurement results of the dynamic friction coefficient.
第1表
第1表の結果から、本発明の現像ローラは、比較例のも
のと比べ表面の動摩擦係数が低減していることが分る。From the results shown in Table 1, it can be seen that the surface dynamic friction coefficient of the developing roller of the present invention is reduced compared to that of the comparative example.
また、フィルミング試験の結果、実施例では、現像ロー
ラ表面にトナーの融着はI!察されなかったが、比較例
では、ローラ表面にほぼ均一にトナーが融着しているの
が認められた。Also, as a result of the filming test, in the example, the toner fusion on the developing roller surface was I! However, in the comparative example, it was observed that the toner was almost uniformly fused to the roller surface.
本発明の現像剤担持体は、表面又は表面近傍番フッ素系
界面活性剤を含有した構成としたことズら、現像剤担持
体表面の動摩擦係数が低減した崎のとなる。Since the developer carrier of the present invention contains a fluorine-based surfactant on or near the surface, the coefficient of dynamic friction on the surface of the developer carrier is reduced.
従って、現像剤担持体の表面上に、選択的に冑荷を保持
させることにより、現像剤担持体表面だ傍に多数の微小
閉電界を形成し、この現像剤担持体上に、必要に応じて
補助剤を外添したトナーよりなる非磁性一成分系現像剤
を供給し、前記微、J・閉電界により前記現像剤を現像
剤担持体表面に相持させ、該担持現像剤によって静電潜
像を可視像化する画像形成方法に9本発明の現像剤担持
体を用いると、充分に帯電した多量の非磁性一成分系現
像剤を現像剤担持体に担持して現像領域に搬送すること
ができ、その結果、トナーフィルミングが発生せず、高
濃度の高品質画像を得ることができる。Therefore, by selectively retaining a charge on the surface of the developer carrier, a large number of minute closed electric fields are formed near the surface of the developer carrier, and as needed, A non-magnetic one-component developer made of toner externally added with an auxiliary agent is supplied, and the developer is supported on the surface of the developer carrier by the fine, J-closed electric field, and the electrostatic latent is caused by the supported developer. When the developer carrier of the present invention is used in an image forming method for visualizing an image, a large amount of sufficiently charged non-magnetic one-component developer is carried on the developer carrier and transported to the development area. As a result, toner filming does not occur, and high-quality images with high density can be obtained.
第1@は本発明の実施に有用な現像剤担持体上にマイク
ロフィールドの電界を形成させた現像装置の一例を示す
現像剤担持体部を中心とした模式断面図である。また、
第2図は第1図で示される装置において、現像剤担持体
上にマイクロフィールドによる閉電界が生成している状
態を説明するための模式断面図である。
更に、第3図(a)−(c)は、本発明の現像剤担持体
の作製過程における表面状態を示す模式断面図である。
また、第4図(a)〜(d)は、本発明の現像剤担持体
の表面の構成例を示す模式断面図である。
10・・静電潜像担持体、20・・現像剤担持体。
30・・・トナー層厚規制部材、40・・トナー供給部
材、50・・・撹拌羽根、60・・・トナー、70・・
・トナータンク、80・・・現像域。
特許出願人 株式会社 リ コThe first @ is a schematic cross-sectional view centered on a developer carrier portion showing an example of a developing device in which a microfield electric field is formed on a developer carrier useful for implementing the present invention. Also,
FIG. 2 is a schematic cross-sectional view for explaining a state in which a closed electric field is generated by a microfield on a developer carrier in the apparatus shown in FIG. Further, FIGS. 3(a) to 3(c) are schematic cross-sectional views showing the surface state during the manufacturing process of the developer carrier of the present invention. Moreover, FIGS. 4(a) to 4(d) are schematic cross-sectional views showing examples of the structure of the surface of the developer carrier of the present invention. 10: Electrostatic latent image carrier, 20: Developer carrier. 30... Toner layer thickness regulating member, 40... Toner supply member, 50... Stirring blade, 60... Toner, 70...
・Toner tank, 80...Development area. Patent applicant Rico Co., Ltd.
Claims (1)
せることにより、現像剤担持体表面近傍に多数の微小閉
電界を形成し、この現像剤担持体上に、必要に応じて補
助剤を外添したトナーよりなる非磁性一成分系現像剤を
供給し、前記微小閉電界により前記現像剤を現像剤担持
体表面に担持させ、該担持現像剤によって静電潜像を可
視像化する画像形成方法に用いる現像剤担持体であって
、少なくともその表面又は表面近傍にフッ素系界面活性
剤が含有されているものであることを特徴とする現像剤
担持体。(1) By selectively retaining electric charges on the surface of the developer carrier, a large number of minute closed electric fields are formed near the surface of the developer carrier, and as needed, A non-magnetic one-component developer made of toner externally added with an adjuvant is supplied, the developer is supported on the surface of the developer carrier by the minute closed electric field, and the electrostatic latent image is made visible by the supported developer. 1. A developer carrier used in an image forming method, characterized in that the developer carrier contains a fluorine-based surfactant at least on the surface or near the surface.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2128676A JPH0422979A (en) | 1990-05-18 | 1990-05-18 | Developer carrying member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2128676A JPH0422979A (en) | 1990-05-18 | 1990-05-18 | Developer carrying member |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0422979A true JPH0422979A (en) | 1992-01-27 |
Family
ID=14990692
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2128676A Pending JPH0422979A (en) | 1990-05-18 | 1990-05-18 | Developer carrying member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0422979A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5478614A (en) * | 1994-10-07 | 1995-12-26 | Minnesota Mining And Manufacturing Company | Infrared sensitive recording medium with fluorocarbon surfactant |
US6668148B2 (en) | 2000-12-20 | 2003-12-23 | Ricoh Company, Ltd. | Latent electrostatic image developing apparatus and image forming apparatus including such developing apparatus |
-
1990
- 1990-05-18 JP JP2128676A patent/JPH0422979A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5478614A (en) * | 1994-10-07 | 1995-12-26 | Minnesota Mining And Manufacturing Company | Infrared sensitive recording medium with fluorocarbon surfactant |
US6668148B2 (en) | 2000-12-20 | 2003-12-23 | Ricoh Company, Ltd. | Latent electrostatic image developing apparatus and image forming apparatus including such developing apparatus |
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