JPH04338977A - Nonmagnetic one-component development method - Google Patents
Nonmagnetic one-component development methodInfo
- Publication number
- JPH04338977A JPH04338977A JP3025060A JP2506091A JPH04338977A JP H04338977 A JPH04338977 A JP H04338977A JP 3025060 A JP3025060 A JP 3025060A JP 2506091 A JP2506091 A JP 2506091A JP H04338977 A JPH04338977 A JP H04338977A
- Authority
- JP
- Japan
- Prior art keywords
- magnetic
- toner
- hydrophobic silica
- developer
- magnetic powder
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims abstract description 36
- 238000011161 development Methods 0.000 title claims abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 115
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 56
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 54
- 239000006247 magnetic powder Substances 0.000 claims abstract description 37
- 239000002245 particle Substances 0.000 claims abstract description 21
- 229920005989 resin Polymers 0.000 claims abstract description 17
- 239000011347 resin Substances 0.000 claims abstract description 17
- 239000011230 binding agent Substances 0.000 claims abstract description 7
- 239000003086 colorant Substances 0.000 claims abstract description 6
- 108091008695 photoreceptors Proteins 0.000 claims description 13
- 230000001105 regulatory effect Effects 0.000 claims description 9
- 239000007787 solid Substances 0.000 abstract description 14
- 230000007423 decrease Effects 0.000 abstract description 4
- 230000004927 fusion Effects 0.000 abstract description 3
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000006231 channel black Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052595 hematite Inorganic materials 0.000 description 1
- 239000011019 hematite Substances 0.000 description 1
- UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920005670 poly(ethylene-vinyl chloride) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- 125000005372 silanol group Chemical group 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
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は非磁性トナーを用いて静
電潜像を現像する接触型の非磁性一成分現像方法に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a contact type nonmagnetic one-component developing method for developing an electrostatic latent image using a nonmagnetic toner.
【0002】0002
【従来の技術】従来から行なわれている静電潜像とトナ
ーを用いて現像する方法には、トナー及びキャリアを主
体とする二成分現像剤を用いる二成分現像方法、あるい
は磁性トナーのみからなる一成分現像剤を用いる一成分
現像方法があり、各々の現像方法に関しては各種提案さ
れている。[Prior Art] Conventional methods of developing using an electrostatic latent image and toner include a two-component developing method using a two-component developer mainly consisting of toner and a carrier, or a two-component developing method using only a magnetic toner. There is a one-component developing method using a one-component developer, and various proposals have been made regarding each developing method.
【0003】非磁性トナーとキャリアを用いる二成分系
の現像方法は一成分系と比較して次のような欠点がある
。
■トナーとキャリアとの混合比をコントロールするため
のトナー濃度センサーが必要である。
■現像剤の寿命が短い。
■現像剤の攪拌機構など取扱いに注意が必要であり現像
機等の装置が大型となる。A two-component developing method using a non-magnetic toner and a carrier has the following disadvantages compared to a one-component developing method. ■A toner concentration sensor is required to control the mixing ratio of toner and carrier. ■The life of the developer is short. ■Care must be taken when handling the developer stirring mechanism, and equipment such as the developing machine becomes large.
【0004】また磁性トナーを用いる一成分系の欠点と
しては以下の点が挙げられる。
■帯電部材がスリーブあるいはブレードでありキャリア
に比べると帯電の安定性にかけ帯電能力も弱い。
■磁気ブラシを均一に形成するための現像機の精度が必
要である。
■転写性、定着性が非磁性トナーに比べ劣り、かつ感光
体の表面への損傷性が大きい。[0004] Further, the following points are listed as disadvantages of the one-component system using magnetic toner. ■The charging member is a sleeve or blade, and compared to a carrier, charging stability and charging ability are weaker. ■The precision of the developing machine is necessary to uniformly form the magnetic brush. (2) Transfer and fixing properties are inferior to non-magnetic toners, and the surface of the photoreceptor is more likely to be damaged.
【0005】これらの問題点を総合的に考え、かつ、装
置の小型化等を合わせて考えると非磁性トナーを用いる
一成分現像方法が極めて有効であるとされ、近年、非磁
性一成分現像方法を用いた現像方式が注目され、いくつ
かは実用化されている。[0005] Considering these problems comprehensively and considering the miniaturization of the device, it is believed that a single-component developing method using non-magnetic toner is extremely effective, and in recent years, non-magnetic single-component developing methods Developing methods using .
【0006】非磁性トナーを用いる一成分現像方法では
、現像剤を担持した現像ロールにトナー層を形成する過
程に於て、現像剤はトナー層を規制するためのブレード
あるいは現像ロール上にトナー層を形成するために設け
られたトナー供給ローラーのみによって摩擦帯電するた
めに充分な摩擦帯電が行われにくい。In the one-component development method using non-magnetic toner, in the process of forming a toner layer on a developing roll carrying a developer, the developer is applied to a blade for regulating the toner layer or to a toner layer on the developing roll. Since triboelectric charging is performed only by the toner supply roller provided for forming the toner, sufficient triboelectric charging is difficult to be performed.
【0007】そのため、非磁性一成分現像方法では、通
常の文字画像をプリントしているかぎりではまったく問
題が無いが、黒ベタ部の多いプリントを行った場合黒ベ
タ部の濃度が低下してしまうという現象が起こることが
ある。これは、前記のトナーの摩擦帯電が充分に行われ
ないため、現像スリーブ上に充分な摩擦帯電性を有する
トナー層が形成されていないために起こるものと考えら
れる。[0007] Therefore, with the non-magnetic one-component development method, there is no problem at all as long as normal character images are printed, but when printing with many solid black areas, the density of the solid black areas decreases. This phenomenon may occur. This is thought to occur because the toner is not sufficiently tribo-electrified, so that a toner layer with sufficient tribo-charging properties is not formed on the developing sleeve.
【0008】充分な摩擦帯電性を有するトナー層を形成
するためには、ブレードあるいはトナー供給ローラーと
の摩擦のみで充分な帯電をすれば良いわけであるが、こ
れに必要ないわゆる現像剤の帯電の立ち上がり特性を良
好にすることが従来技術では困難であった。[0008] In order to form a toner layer with sufficient triboelectric charging properties, it is sufficient to perform sufficient charging only by friction with the blade or toner supply roller, but the so-called developer charging required for this is sufficient. It has been difficult with the prior art to improve the rise characteristics of .
【0009】[0009]
【発明が解決しようとする課題】本発明は非磁性トナー
を用いる非磁性一成分現像方法に於て、きわめて良好な
現像特性を得るために、帯電の立ち上がりが良好で、黒
ベタ画像の濃度低下がなく、かつ非磁性一成分接触方式
で生じ易い欠点である現像ロールへのトナーの融着、感
光体表面に対する損傷の少ない現像方法を提供するため
のものである。[Problems to be Solved by the Invention] In order to obtain extremely good development characteristics in a non-magnetic one-component developing method using non-magnetic toner, the present invention aims to improve the charging start-up and reduce the density of solid black images. The object of the present invention is to provide a developing method that is free from toner fusing to the developing roll and damage to the photoreceptor surface, which are disadvantages that tend to occur in non-magnetic one-component contact systems.
【0010】0010
【課題を解決するための手段】本発明者等は接触型の非
磁性一成分現像方法における従来技術の問題点を解決す
べく鋭意検討した結果、非磁性トナーの表面への後処理
剤に技術的工夫を加えることによって、良好な帯電性を
得ながら黒ベタ画像の濃度低下をなくし、現像ロールへ
のトナーの融着及び感光体への損傷の発生が少ない非磁
性一成分現像方法を得ることができることが分った。[Means for Solving the Problems] As a result of intensive studies to solve the problems of the conventional contact type non-magnetic one-component developing method, the present inventors have developed a technology for post-processing agents for the surface of non-magnetic toner. To obtain a non-magnetic one-component developing method that eliminates a decrease in the density of a solid black image while obtaining good charging properties, and reduces the occurrence of toner fusion to a developing roll and damage to a photoconductor by adding a specific device. It turns out that it is possible.
【0011】すなわち、本発明は、現像ロールに現像剤
を供給し、規制部材により現像剤の薄層を現像ロール上
に形成するとともに該現像剤に電荷を与え、静電潜像を
保持する感光体に接触させて静電潜像を現像し、ついで
用紙に転写を行う接触型の非磁性一成分現像方法におい
て、前記現像剤が結着剤樹脂と着色剤を主成分とした非
磁性トナーの表面に疎水性シリカと磁性粉が付着したも
のであって、かつ、該疎水性シリカはその一部が非磁性
トナー表面に固着した状態をなし、磁性粉は0.5〜3
.0μm の粒子であることを特徴とする非磁性一成分
現像方法である。That is, the present invention provides a photosensitive material that supplies a developer to a developing roll, forms a thin layer of the developer on the developing roll using a regulating member, and charges the developer to retain an electrostatic latent image. In a contact-type non-magnetic one-component developing method in which an electrostatic latent image is developed by contacting the body and then transferred to paper, the developer is a non-magnetic toner whose main components are a binder resin and a colorant. Hydrophobic silica and magnetic powder are attached to the surface, and a part of the hydrophobic silica is stuck to the non-magnetic toner surface, and the magnetic powder is 0.5 to 3
.. This is a non-magnetic one-component developing method characterized by particles having a diameter of 0 μm.
【0012】以下、本発明について詳細に説明する。第
1図は、本発明の接触型の非磁性一成分現像方法に使用
する現像装置の概略構成図である。図中、1は円筒状の
静電潜像保持体である感光体ドラム、2はホッパー、3
は現像剤、4はドクターブレードなどの規制部材、5は
トナー担持層を設けた現像ロール、6はトナー供給ロー
ル、7は攪拌機である。この現像装置において、感光体
ドラム1の表面には、電子写真法によって静電潜像が形
成される。ホッパー2内には現像剤3が収容されており
、現像剤は、規制部材4によって現像ロール5のトナー
担持層表面に一定の層厚になるように担持され、感光体
の表面に搬送される。その際現像剤は規制部材によって
摩擦帯電されるが、規制部材は、直流または交流電源に
接続され、トナー担持層と規制部材の間に電界が発生す
るようにしてもよい。現像ロール5のトナー担持層に担
持された現像剤は、現像ロール5の回転により搬送され
て、静電潜像を有する感光体ドラム1と接触し、静電潜
像の顕像化が行われる。The present invention will be explained in detail below. FIG. 1 is a schematic diagram of a developing device used in the contact type non-magnetic one-component developing method of the present invention. In the figure, 1 is a photosensitive drum which is a cylindrical electrostatic latent image holder, 2 is a hopper, and 3
4 is a developer, 4 is a regulating member such as a doctor blade, 5 is a developing roll provided with a toner carrying layer, 6 is a toner supply roll, and 7 is an agitator. In this developing device, an electrostatic latent image is formed on the surface of the photosensitive drum 1 by electrophotography. A developer 3 is stored in the hopper 2, and the developer is carried by a regulating member 4 on the surface of the toner carrying layer of the developing roll 5 to a constant layer thickness, and is conveyed to the surface of the photoreceptor. . At this time, the developer is triboelectrically charged by the regulating member, and the regulating member may be connected to a direct current or alternating current power source to generate an electric field between the toner carrying layer and the regulating member. The developer carried on the toner carrying layer of the developing roll 5 is conveyed by the rotation of the developing roll 5 and comes into contact with the photoreceptor drum 1 having an electrostatic latent image, so that the electrostatic latent image is visualized. .
【0013】トナー担持層は、弾性を有するロールの上
に形成されるが、ロールは、バイアス電圧が印加できる
ように導電性の材料よりなるか、または導電性層を有す
るのが好ましい。トナー担持層としては、適度の弾性を
備えた、肉薄樹脂層よりなり、例えば、含フッ素樹脂、
シリコン系樹脂、ポリエステル樹脂、ポリカーボネート
樹脂など、膜形成性を有する樹脂が使用される。トナー
担持層の厚さは、10〜200μm の範囲に形成され
る。また、ロールを構成する弾性材料としては、シリコ
ンゴム等の各種ゴム、スポンジゴム、ウレタンフォーム
等が使用され、これらには導電性粉末が含有されていて
もよい。また、表面には導電性塗料が塗布されたもので
あってもよい。The toner carrying layer is formed on an elastic roll, and the roll is preferably made of a conductive material or has a conductive layer so that a bias voltage can be applied. The toner carrying layer is made of a thin resin layer with appropriate elasticity, such as fluorine-containing resin,
Resins having film-forming properties are used, such as silicone resins, polyester resins, and polycarbonate resins. The thickness of the toner carrying layer is formed in a range of 10 to 200 μm. Further, as the elastic material constituting the roll, various rubbers such as silicone rubber, sponge rubber, urethane foam, etc. are used, and these may contain conductive powder. Further, the surface may be coated with a conductive paint.
【0014】本発明において使用する一成分現像剤を構
成する非磁性トナーは、結着剤樹脂と着色剤とを主成分
とするものである。The non-magnetic toner constituting the one-component developer used in the present invention contains a binder resin and a colorant as main components.
【0015】結着剤樹脂としては、従来電子写真用乾式
トナーに使用されているもののほか、電荷制御性等の点
で使用できなかったものが全て使用できる。例えば、ポ
リスチレン、ポリエステル、エチレン−塩化ビニル共重
合体、エチレン−酢酸ビニル共重合体、ポリアミド、ポ
リエチレン、マレイン酸樹脂、アクリル系樹脂、エポキ
シ樹脂、キシレン樹脂、クマロン樹脂、ケトン樹脂、石
油樹脂、フェノール樹脂等があげられる。[0015] As the binder resin, in addition to those conventionally used in dry toners for electrophotography, any resin that could not be used due to charge controllability etc. can be used. For example, polystyrene, polyester, ethylene-vinyl chloride copolymer, ethylene-vinyl acetate copolymer, polyamide, polyethylene, maleic acid resin, acrylic resin, epoxy resin, xylene resin, coumaron resin, ketone resin, petroleum resin, phenol. Examples include resin.
【0016】また、着色剤としては、例えば、カーボン
ブラック、アセチレンブラック、ランプブラック、チャ
ンネルブラック、ファーナルブルー、パーマネントブル
ー、ニグロシンブルー、フタロシアニンブルー、ローズ
ベンガル、C.I.ピグメントレッド122、C.I.
ピグメントイエロー12等があげられる。これら着色剤
は、結着剤樹脂100重量部に対して1〜10重量部の
範囲で適宜配合される。上記非磁性トナーには、所望に
より他の成分、例えば公知の電荷制御剤が含有されてい
てもよい。非磁性トナーは、約30μm よりも小さな
粒径を有するものが好ましく使用される。Examples of colorants include carbon black, acetylene black, lamp black, channel black, funeral blue, permanent blue, nigrosine blue, phthalocyanine blue, rose bengal, C.I. I. Pigment Red 122, C. I.
Pigment Yellow 12 etc. can be mentioned. These colorants are appropriately blended in an amount of 1 to 10 parts by weight based on 100 parts by weight of the binder resin. The non-magnetic toner may contain other components, such as a known charge control agent, if desired. Non-magnetic toners having a particle size of less than about 30 μm are preferably used.
【0017】本発明において、上記非磁性トナーには、
疎水性シリカが配合されるが、その際、トナー粒子の表
面に疎水性シリカの一部を固着させ、一部を付着させた
状態で保持させる。本発明で称する固着とは、トナー粒
子と疎水性シリカが混合中に点接触し、混合時の圧縮力
、摩擦力及び衝撃力によって、該接触点で少なくともト
ナー粒子あるいは疎水性シリカの何れか一方がその融点
以上となる熱が瞬時に発生し、融着による固着現象のこ
とを示し、トナー粒子に疎水性シリカの一部が埋没した
状態をいう。一方、付着とはトナー粒子表面に疎水性シ
リカがまぶされている状態を示し、トナー粒子に疎水性
シリカが埋没していない状態をいう。In the present invention, the non-magnetic toner includes:
Hydrophobic silica is blended, and at that time, a portion of the hydrophobic silica is fixed to the surface of the toner particles, and a portion of the hydrophobic silica is held in an attached state. The adhesion referred to in the present invention means that toner particles and hydrophobic silica come into point contact during mixing, and at least either the toner particles or the hydrophobic silica at the contact point is caused by compressive force, frictional force, and impact force during mixing. Heat is generated instantaneously to a temperature higher than the melting point of the silica, indicating a phenomenon of adhesion due to fusion, and refers to a state in which a portion of the hydrophobic silica is embedded in the toner particles. On the other hand, adhesion refers to a state in which hydrophobic silica is sprinkled on the surface of toner particles, and refers to a state in which hydrophobic silica is not embedded in toner particles.
【0018】非磁性トナーに疎水性シリカの一部を固着
させ、一部を付着させた状態で保持させるためには、疎
水性シリカを通常の使用量よりも多量、好ましくは非磁
性トナーに対し、0.6重量%以上添加し、疎水性シリ
カを2回以上に分けて混合することにより行われる。そ
の場合、非磁性トナーに固着させる疎水性シリカと付着
させる疎水性シリカの割合は、40:60〜90:10
の範囲にするのが好ましい。[0018] In order to fix a part of the hydrophobic silica to the non-magnetic toner and keep the part attached, a larger amount of hydrophobic silica than usual is used, preferably for the non-magnetic toner. , 0.6% by weight or more, and the hydrophobic silica is mixed in two or more portions. In that case, the ratio of hydrophobic silica to be fixed to the non-magnetic toner and hydrophobic silica to be attached is 40:60 to 90:10.
It is preferable to keep it within the range of .
【0019】非磁性トナーに疎水性シリカの一部を固着
させ、一部を付着させるためには、通常の粉体用混合機
であるヘンシェルミキサー、スーパーミキサー等の混合
機のほかハイブリダイザー、オングミル等のいわゆる表
面改質機も用いて行うことができる。ヘンシェルミキサ
ー、スーパーミキサー等の粉体混合機を用いる場合には
、比較的長時間の処理時間が必要とされるが、いわゆる
表面改質機を用いる場合には、比較的短時間の処理で同
様の効果が得られ効率的である。例えば、まず、非磁性
トナーに疎水性シリカの所定量を配合し、トナー粒子表
面に疎水性シリカが結着剤樹脂の融点近傍での加熱によ
り固着するまで上記の混合機で混合処理をした後、さら
に疎水性シリカの残りの量を上記非磁性トナーに添加し
、温和な混合条件で短時間混合する。In order to fix a part of the hydrophobic silica to the non-magnetic toner and make it adhere to the non-magnetic toner, it is necessary to use a mixer such as a Henschel mixer, a super mixer, etc., which are normal powder mixers, a hybridizer, an Ongmill, etc. This can also be carried out using a so-called surface modification machine such as . When using a powder mixer such as a Henschel mixer or a super mixer, a relatively long processing time is required, but when using a so-called surface modification machine, the same process can be achieved in a relatively short time. It is efficient and has the following effects. For example, first, a predetermined amount of hydrophobic silica is blended into a non-magnetic toner, and the mixture is mixed with the above-mentioned mixer until the hydrophobic silica is fixed on the surface of the toner particles by heating near the melting point of the binder resin. Then, the remaining amount of hydrophobic silica is added to the non-magnetic toner and mixed for a short time under mild mixing conditions.
【0020】本発明において使用する疎水性シリカとし
ては、通常の親水性シリカ分子の末端シラノール基を有
機ケイ素ハロゲン化物やアルコール類と置換することに
より容易に得ることができる。この様な疎水性シリカ微
粉末は、市販品としても容易に入手することができる(
例えば、日本アエロジル社製アエロジルR−972、ヘ
キスト社製H2000等)。The hydrophobic silica used in the present invention can be easily obtained by replacing the terminal silanol group of a conventional hydrophilic silica molecule with an organosilicon halide or alcohol. Such hydrophobic silica fine powder is easily available as a commercial product (
For example, Aerosil R-972 manufactured by Nippon Aerosil, H2000 manufactured by Hoechst, etc.).
【0021】次に本発明の他の特徴である磁性粉につい
て説明する。本発明においては非磁性トナーのトナー粒
子表面には前記の疎水性シリカとともに磁性粉を付着さ
せるものである。磁性粉をトナー粒子に付着させること
によって帯電の立ち上がり特性を良好にして黒ベタ部が
多い原稿での画像濃度の低下を防ぐものである。磁性粉
を非磁性トナーに付着させると帯電の立ち上がり特性が
なぜ良好になるのかについては、明確ではないが、おそ
らく磁性粉を付着させることによってトナー粒子表面が
不均一になるためと思われる。帯電の立ち上がり特性の
みに着目すれば、特に磁性粉の大きさを限定しなくても
ある程度の目的を達成することができるが、現像ロール
へのトナーの融着、感光体表面への損傷の発生を防止す
るためには非磁性トナーに添加する磁性粉の大きさは重
要な因子となる。すなわち、本発明に使用される磁性粉
の大きさは0.5〜3.0μm でなければならない。
その理由は、0.5μm 未満であるとクリーニングブ
レードによる感光体表面の磁性粉のクリーニングがされ
にくくなるため損傷し易く、一方3.0μm より大き
い場合には感光体と現像ロールとの接触、あるいは感光
体とクリーニングブレードとの接触の間で磁性粉が押し
つけられ、損傷し易い。Next, magnetic powder, which is another feature of the present invention, will be explained. In the present invention, magnetic powder is attached to the surface of the toner particles of the non-magnetic toner together with the above-mentioned hydrophobic silica. By adhering magnetic powder to toner particles, the charge build-up characteristics are improved and image density is prevented from decreasing in originals with many solid black areas. Although it is not clear why the charging characteristics improve when magnetic powder is attached to non-magnetic toner, it is probably because the surface of the toner particles becomes non-uniform by attaching magnetic powder. If we focus only on the charging rise characteristics, it is possible to achieve the objective to some extent without particularly limiting the size of the magnetic powder, but this may cause the toner to fuse to the developing roll and damage the photoreceptor surface. In order to prevent this, the size of the magnetic powder added to the non-magnetic toner is an important factor. That is, the size of the magnetic powder used in the present invention must be 0.5 to 3.0 μm. The reason for this is that if the thickness is less than 0.5 μm, it becomes difficult for the cleaning blade to clean the magnetic powder on the surface of the photoreceptor, causing damage, whereas if it is larger than 3.0 μm, contact between the photoreceptor and the developing roll, or Magnetic powder is pressed between the contact between the photoreceptor and the cleaning blade and is easily damaged.
【0022】磁性粉は0.5〜3.0μm の粒子径を
もつ磁性粉をそのまま非磁性トナーの表面に付着させて
もよいし、一般的に市販されている磁性粉は一次粒子径
が0.2〜0.4μm であって、複数の一次粒子によ
り5〜10μm の凝集体を形成しているため、ヘンシ
ェルミキサー等の混合機に該磁性粉と非磁性トナーとを
入れた後、混合機の攪拌羽根の回転数を調整しながら5
〜10μm の凝集体を分散させて0.5〜3.0μm
の磁性粉を形成して非磁性トナーの表面に付着せしめ
てもよい。Magnetic powder having a particle size of 0.5 to 3.0 μm may be directly attached to the surface of a non-magnetic toner, or magnetic powder generally available on the market may have a primary particle size of 0. .2 to 0.4 μm, and multiple primary particles form aggregates of 5 to 10 μm. Therefore, after putting the magnetic powder and non-magnetic toner into a mixer such as a Henschel mixer, 5 while adjusting the rotation speed of the stirring blade.
~10μm aggregates are dispersed to 0.5~3.0μm
A magnetic powder may be formed and attached to the surface of the non-magnetic toner.
【0023】また、本発明に使用される磁性粉の形状は
磁性粉が非磁性トナーから離脱した場合に感光体を傷つ
けないため、立方状であることが好ましい。非磁性トナ
ーへの磁性粉の付着量は多すぎると感光体への傷の発生
が多くなり、少ないと帯電性の立ち上がりの向上に寄与
しないため、非磁性トナーに対して0.1〜0.8重量
%であることが好ましい。このような磁性粉としては、
鉄、コバルト、ニッケル、マンガン、亜鉛等の化合物で
あるマグネタイト、ヘマタイト、フェライト等であって
、具体的には戸田工業社製のEPT−500やEPT−
1000、あるいはチタン工業社製のBL−220やB
L−200等がある。[0023] Furthermore, the shape of the magnetic powder used in the present invention is preferably cubic in order to prevent damage to the photoreceptor when the magnetic powder separates from the non-magnetic toner. If the amount of magnetic powder attached to the non-magnetic toner is too large, it will cause more scratches on the photoreceptor, and if it is too small, it will not contribute to improving the rise of chargeability. Preferably, it is 8% by weight. As such magnetic powder,
Magnetite, hematite, ferrite, etc., which are compounds of iron, cobalt, nickel, manganese, zinc, etc., specifically EPT-500 and EPT- manufactured by Toda Kogyo Co., Ltd.
1000, or BL-220 or B manufactured by Titanium Kogyo Co., Ltd.
There are L-200 etc.
【0024】本発明で疎水性シリカ(一部固着、一部付
着)と磁性粉を付着させるには、次のような方法で行う
ことができ、製造コストの点から(1)あるいは(2)
の方法で行うことが好ましい。In the present invention, hydrophobic silica (partly fixed, partially attached) and magnetic powder can be attached by the following method, and from the viewpoint of manufacturing cost, (1) or (2) is preferred.
It is preferable to carry out this method.
【0025】(1)非磁性トナー、磁性粉及び疎水性シ
リカを混合機に入れて、トナー粒子の表面に磁性粉を付
着し、かつ疎水性シリカを固着させた後、再度疎水性シ
リカを入れて疎水性シリカを付着させる方法。(2)非
磁性トナーと疎水性シリカを混合機に入れて、トナー粒
子の表面に疎水性シリカを固着させた後、磁性粉と疎水
性シリカを入れて磁性粉と疎水性シリカを付着させる方
法。
(3)非磁性トナーと磁性粉を混合機に入れて、トナー
粒子の表面に磁性粉を付着した後、疎水性シリカを入れ
て固着処理を行い、再度疎水性シリカを混合機に入れて
疎水性シリカを付着させる方法。
(4)非磁性トナーと疎水性シリカを混合機に入れて、
トナー粒子の表面に疎水性シリカを固着させた後、磁性
粉を入れて付着処理を行い、再度疎水性シリカを混合機
に入れて疎水性シリカを付着させる方法。
(5)非磁性トナーと疎水性シリカを混合機に入れて、
トナー粒子の表面に疎水性シリカを固着させた後、再度
疎水性シリカを入れて付着処理を行い、次に磁性粉を混
合機に入れて磁性粉を付着させる方法。(1) Put the non-magnetic toner, magnetic powder and hydrophobic silica into a mixer, and after adhering the magnetic powder to the surface of the toner particles and fixing the hydrophobic silica, add the hydrophobic silica again. method of attaching hydrophobic silica. (2) A method in which non-magnetic toner and hydrophobic silica are placed in a mixer to adhere the hydrophobic silica to the surface of the toner particles, and then magnetic powder and hydrophobic silica are placed in the mixer to adhere the magnetic powder and hydrophobic silica. . (3) Put the non-magnetic toner and magnetic powder into a mixer, and after adhering the magnetic powder to the surface of the toner particles, add hydrophobic silica and perform fixing treatment, then put the hydrophobic silica into the mixer again to make it hydrophobic. How to attach silica. (4) Put the non-magnetic toner and hydrophobic silica into a mixer,
A method in which hydrophobic silica is adhered to the surface of toner particles, then magnetic powder is added to perform adhesion treatment, and then hydrophobic silica is placed in a mixer again to adhere hydrophobic silica. (5) Put the non-magnetic toner and hydrophobic silica into a mixer,
A method in which hydrophobic silica is fixed to the surface of toner particles, then hydrophobic silica is added again to perform the adhesion treatment, and then magnetic powder is placed in a mixer to make the magnetic powder adhere.
【0026】[0026]
【実施例】以下、実施例にしたがって本発明を説明する
がこれに限定されるものではない。なお、以下に記す部
とは重量部を示す。[Examples] The present invention will be explained below with reference to Examples, but the present invention is not limited thereto. Note that the parts described below refer to parts by weight.
【0027】実施例1
下記の配合で原料の混合、溶融混練、粉砕分級を行い、
平均粒子径が12μmの非磁性トナーを得た。
スチレンアクリル共重合体
92部 (
藤倉化成社製 TTR−563) ポリプ
ロピレンワックス
2部 (三洋化成工業社
製 ビスコール550P) クロム含金属
染料
1部 (オリエント化学
工業社製 ボントロンS−34) カーボ
ンブラック
5部 (三菱化成
工業社製 MA−100)上記の非磁性トナーに疎水
性シリカ(ヘキスト社製、商品名H2000)を0.4
重量%とマグネタイト(戸田工業社製、商品名EPT−
500)を0.5重量%添加し、ヘンシェルミキサーで
冷却水を通しながら30分間攪拌し、非磁性トナーの表
面に疎水性シリカの固着と磁性粉の付着を行った。さら
に、同じ疎水性シリカを0.2重量%添加し2分間攪拌
することによって、本発明に使用する現像剤を得た。該
現像剤の表面を電子顕微鏡で観察したところ、現像剤の
表面のマグネタイトは1.0〜2.0μm の大きさに
凝集されていた。得られた現像剤を用いて、第1図の現
像機構を有する市販の非磁性一成分現像方式のプリンタ
ー(リコー社製 LP1060−SP3)を用いて、
常温常湿(20℃、60%RH)、低温低湿(10℃、
15%RH)及び高温高湿(30℃、80%RH)の各
環境下においてプリントを行ったところ、10000枚
をプリントしても初期画像と比較して変化がなく、黒ベ
タ部の均一性も良好であった。また、現像ロールへのト
ナーの融着、感光体ドラムへの損傷の発生も全くなく、
良好な結果であった。Example 1 The raw materials were mixed, melt-kneaded, crushed and classified according to the following composition,
A non-magnetic toner having an average particle diameter of 12 μm was obtained. Styrene acrylic copolymer
92 copies (
Manufactured by Fujikura Kasei Co., Ltd. TTR-563) Polypropylene wax
Part 2 (Viscol 550P manufactured by Sanyo Chemical Industries, Ltd.) Chromium-containing metal dye
1 part (Orient Chemical Industry Co., Ltd. Bontron S-34) Carbon black
5 parts (MA-100, manufactured by Mitsubishi Chemical Industries, Ltd.) 0.4 parts of hydrophobic silica (manufactured by Hoechst, trade name H2000) was added to the above non-magnetic toner.
Weight% and magnetite (manufactured by Toda Kogyo Co., Ltd., product name: EPT-
500) was added in an amount of 0.5% by weight, and the mixture was stirred for 30 minutes while passing cooling water through a Henschel mixer to fix hydrophobic silica and magnetic powder on the surface of the non-magnetic toner. Further, 0.2% by weight of the same hydrophobic silica was added and stirred for 2 minutes to obtain a developer used in the present invention. When the surface of the developer was observed using an electron microscope, it was found that the magnetite on the surface of the developer was aggregated to a size of 1.0 to 2.0 μm. Using the obtained developer, a commercially available non-magnetic one-component development printer (LP1060-SP3 manufactured by Ricoh Co., Ltd.) having the developing mechanism shown in Fig. 1 was used.
Normal temperature and humidity (20℃, 60%RH), low temperature and low humidity (10℃,
When printing was performed under various environments (15% RH) and high temperature and high humidity (30°C, 80% RH), there was no change compared to the initial image even after printing 10,000 sheets, and the uniformity of the black solid area was improved. was also good. Additionally, there is no occurrence of toner fusing to the developing roll or damage to the photoreceptor drum.
The results were good.
【0028】比較例1
実施例1の非磁性トナーに実施例1と同じ疎水性シリカ
のみを0.6重量%添加し、ヘンシェルミキサーにて2
分間攪拌して比較用の現像剤を得た。実施例1と同様に
市販のプリンター(リコー社製 LP1060−SP
3)を用いて、各環境条件においてプリントを行った。
その結果、各環境下において黒ベタ画像で現像ロールの
2周期以降と思われる部分について濃度が低下し、均一
な画像が得られなかった。また、低温低湿においては画
像濃度の低下が顕著にあらわれた。Comparative Example 1 0.6% by weight of only the same hydrophobic silica as in Example 1 was added to the non-magnetic toner of Example 1, and 2% by weight was added in a Henschel mixer.
A comparative developer was obtained by stirring for a minute. As in Example 1, a commercially available printer (LP1060-SP manufactured by Ricoh Co., Ltd.
3) was used to print under each environmental condition. As a result, under each environment, the density of the black solid image decreased in the portion that appeared to be after the second cycle of the developing roll, and a uniform image could not be obtained. Further, at low temperature and low humidity, a significant decrease in image density appeared.
【0029】比較例2
実施例1の非磁性トナーに実施例1と同じ疎水性シリカ
を0.4重量%添加し、ヘンシェルミキサーで冷却水を
通しながら、30分間攪拌し、疎水性シリカを固着させ
た。さらに、同じ疎水性シリカを0.2重量%添加し、
2分間攪拌することによって比較用の現像剤を得た。実
施例1と同様に市販のプリンター(リコー社製 LP
1060−SP3)を用いて、各環境条件においてプリ
ントを行った。その結果、各環境下において黒ベタ画像
で現像ロールの2周期以降と思われる部分について濃度
が低下し、均一な画像が得られなかった。以上の結果を
まとめると表1のようになる。なお、表中の画像濃度は
マクベス反射濃度計で測定し、カブリはハンター白色度
計で測定した。また、黒ベタ均一性は黒ベタ画像を目視
により評価し、黒ベタ画像が均一なものを○、黒ベタ画
像にムラがあるものを×とした。Comparative Example 2 0.4% by weight of the same hydrophobic silica as in Example 1 was added to the non-magnetic toner of Example 1, and the mixture was stirred for 30 minutes while passing cooling water through a Henschel mixer to fix the hydrophobic silica. I let it happen. Furthermore, 0.2% by weight of the same hydrophobic silica was added,
A comparative developer was obtained by stirring for 2 minutes. As in Example 1, a commercially available printer (Ricoh LP
1060-SP3) under each environmental condition. As a result, under each environment, the density of the black solid image decreased in the portion that appeared to be after the second cycle of the developing roll, and a uniform image could not be obtained. Table 1 summarizes the above results. In addition, the image density in the table was measured with a Macbeth reflection densitometer, and the fog was measured with a Hunter whiteness meter. Furthermore, the black solid uniformity was evaluated by visual inspection of the black solid image, and a uniform black solid image was evaluated as ○, and a black solid image with unevenness was evaluated as poor.
【0030】[0030]
【表1】
次に前記の実施例1、比較例1及び比較例2の現像剤に
ついて、摩擦帯電の立ち上がり特性を評価した。測定法
は以下の通りである。
■ノンコート鉄粉キャリア100部と現像剤10部をビ
ーカーに入れる。
■ビーカー中の試料をマグネットスターラーで攪拌し、
マグネチックスターラーの回転数ごとに摩擦帯電量を測
定する。
なお、この際摩擦帯電量の測定はマグネットブローオフ
法を用いた。マグネットブローオフ法は、磁力の差によ
って現像剤とキャリアを分離してキャリアに残った電荷
を測定するものである。測定結果を表2に示し、その結
果のグラフを図2に示す。表2及び図2から明らかなよ
うに実施例1の現像剤は、少ない回転数で摩擦帯電量が
飽和値に達し、且つ高い値を示していることがわかる。[Table 1] Next, the triboelectric charging build-up characteristics of the developers of Example 1, Comparative Example 1, and Comparative Example 2 were evaluated. The measurement method is as follows. ■Put 100 parts of non-coated iron powder carrier and 10 parts of developer into a beaker. ■Stir the sample in the beaker with a magnetic stirrer,
Measure the amount of triboelectric charge at each rotation speed of the magnetic stirrer. At this time, the amount of triboelectric charge was measured using a magnetic blow-off method. The magnetic blow-off method separates the developer from the carrier using a difference in magnetic force and measures the charge remaining on the carrier. The measurement results are shown in Table 2, and a graph of the results is shown in FIG. As is clear from Table 2 and FIG. 2, in the developer of Example 1, the amount of triboelectric charge reaches a saturation value at a small number of revolutions and exhibits a high value.
【0031】[0031]
【表2】[Table 2]
【0032】[0032]
【発明の効果】本発明は以上のように、疎水性シリカの
一部を非磁性トナーの表面に固着させ、一部を付着させ
、さらに磁性粉の大きさが0.5〜3.0μmになるよ
うに付着させたものであるから、現像剤の帯電の立ち上
がりが早く、かつ現像ロールへのトナーの融着や感光体
ドラムの損傷の発生を防止することができる。したがっ
て、本発明によれば、黒ベタ画像の濃度低下がなく均一
な画像のプリントを得ることができる。Effects of the Invention As described above, the present invention fixes a part of the hydrophobic silica to the surface of a non-magnetic toner, adheres a part of it, and further increases the size of the magnetic powder to 0.5 to 3.0 μm. Since the toner is attached in such a manner that the developer is charged quickly, it is possible to prevent the toner from fusing to the developing roll and damaging the photoreceptor drum. Therefore, according to the present invention, it is possible to print a uniform image without decreasing the density of a solid black image.
第1図は、本発明を実施するための一成分現像装置の概
略断面図である。1…感光体ドラム、2…ホッパー、3
…現像剤、4…規制部材、5…現像ロール、6…トナー
供給ロール、7…攪拌機。FIG. 1 is a schematic sectional view of a one-component developing device for carrying out the present invention. 1...Photosensitive drum, 2...Hopper, 3
...developer, 4...regulating member, 5...developing roll, 6...toner supply roll, 7...stirrer.
Claims (3)
材により現像剤の薄層を現像ロール上に形成するととも
に該現像剤に電荷を与え、静電潜像を保持する感光体に
接触させて静電潜像を現像し、ついで用紙に転写を行う
接触型の非磁性一成分現像方法において、前記現像剤が
結着剤樹脂と着色剤を主成分とした非磁性トナーの表面
に疎水性シリカと磁性粉が付着したものであって、かつ
、該疎水性シリカはその一部が非磁性トナー表面に固着
した状態をなし、磁性粉は0.5〜3.0μm の粒子
であることを特徴とする非磁性一成分現像方法。1. Supplying a developer to a developing roll, forming a thin layer of the developer on the developing roll using a regulating member, applying an electric charge to the developer, and bringing it into contact with a photoreceptor holding an electrostatic latent image. In a contact-type non-magnetic one-component development method in which an electrostatic latent image is developed using a wafer and then transferred to paper, the developer has a hydrophobic property on the surface of a non-magnetic toner whose main components are a binder resin and a colorant. Silica and magnetic powder are attached, and part of the hydrophobic silica is stuck to the non-magnetic toner surface, and the magnetic powder is particles of 0.5 to 3.0 μm. Characteristic non-magnetic one-component development method.
に対し、0.6重量%以上であることを特徴とする請求
項1記載の非磁性一成分現像方法。2. The non-magnetic one-component developing method according to claim 1, wherein the amount of hydrophobic silica deposited is 0.6% by weight or more based on the non-magnetic toner.
が非磁性トナーに対し0.1〜0.8重量%であること
を特徴とする請求項1記載の非磁性一成分現像方法。3. The non-magnetic one-component developing method according to claim 1, wherein the magnetic powder has a cubic shape and the amount of adhesion is 0.1 to 0.8% by weight based on the non-magnetic toner. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3025060A JP2607398B2 (en) | 1991-01-28 | 1991-01-28 | Non-magnetic one-component development method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3025060A JP2607398B2 (en) | 1991-01-28 | 1991-01-28 | Non-magnetic one-component development method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04338977A true JPH04338977A (en) | 1992-11-26 |
JP2607398B2 JP2607398B2 (en) | 1997-05-07 |
Family
ID=12155384
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3025060A Expired - Lifetime JP2607398B2 (en) | 1991-01-28 | 1991-01-28 | Non-magnetic one-component development method |
Country Status (1)
Country | Link |
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JP (1) | JP2607398B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003065125A1 (en) * | 2002-01-28 | 2003-08-07 | Zeon Corporation | Developing agent for electrostatic image development |
-
1991
- 1991-01-28 JP JP3025060A patent/JP2607398B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003065125A1 (en) * | 2002-01-28 | 2003-08-07 | Zeon Corporation | Developing agent for electrostatic image development |
Also Published As
Publication number | Publication date |
---|---|
JP2607398B2 (en) | 1997-05-07 |
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