JPH021881A - How to develop an electrostatic latent image - Google Patents
How to develop an electrostatic latent imageInfo
- Publication number
- JPH021881A JPH021881A JP63143172A JP14317288A JPH021881A JP H021881 A JPH021881 A JP H021881A JP 63143172 A JP63143172 A JP 63143172A JP 14317288 A JP14317288 A JP 14317288A JP H021881 A JPH021881 A JP H021881A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- latent image
- conveying member
- coating layer
- electrostatic latent
- 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
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/06—Apparatus for electrographic processes using a charge pattern for developing
- G03G15/08—Apparatus for electrographic processes using a charge pattern for developing using a solid developer, e.g. powder developer
- G03G15/0806—Apparatus for electrographic processes using a charge pattern for developing using a solid developer, e.g. powder developer on a donor element, e.g. belt, roller
- G03G15/0818—Apparatus for electrographic processes using a charge pattern for developing using a solid developer, e.g. powder developer on a donor element, e.g. belt, roller characterised by the structure of the donor member, e.g. surface properties
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Dry Development In Electrophotography (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
五揉分災
本発明は非磁性1成分系トナーを用いた静電潜隆の現像
方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for developing electrostatic latent ridges using a non-magnetic one-component toner.
従来技末
従来、非磁性1成分系トナー(一般に着色樹脂粒子より
なる)を用いた静電潜像の現像方法としてトナー搬送部
材上にこの部材との摩擦により所望極性に帯電させたト
ナーを薄層状に形成し、これを、前記部材と接するか又
は近接して配置された静電潜像保持体(静電潜像を保持
した、電子写真感光体、静電記録体等)の潜像面に直接
接触させて現像するいわゆる接触現像法が広く採用され
ている。この方法でトナー搬送部材としては一般に金属
ローラー上に被覆層を設けたもの(現像ローラーと呼ば
れる)が使用されているが、このような現像ローラーに
は接触現像用として種々の機能が必要なため1例えば現
像ローラーと組合される静電潜像保持体がセレン感光体
のような剛体の場合、現像ローラーには■必要な現像ニ
ップが得られるように被覆層は柔軟であること、■当接
による圧縮力に対して充分な回復性を持つこと、■所望
の現像特性を得るため、芯金上の被覆層は均一であるこ
と、又、更に重要な現像ローラーの表面或いは表面近傍
の性質として、■常に安定してトナーに所望の帯電極性
や帯電量を付与すること、■トナーとの離型性が良く、
トナーがフィルミングしないこと、■均一なトナー薄層
を形成すめために適切な表面粗さ(数μm以下)を有す
ること、■当接時の摩擦抵抗によるビビリなどを低減す
るために滑性があること、■耐17耗性があること等が
要求されている。なお■に関してはトナーのフィルミン
グが生じると、トナー帯電量が変化し、現像ローラー上
のトナー付着量にムラが生じ、またその結果、画像ムラ
を生じるという不都合がある。Conventional Techniques Conventionally, as a method for developing electrostatic latent images using non-magnetic one-component toner (generally made of colored resin particles), a thin layer of toner charged to a desired polarity by friction with the toner conveying member is deposited on the toner conveying member. The latent image surface of an electrostatic latent image holder (an electrophotographic photoreceptor, an electrostatic recording medium, etc. that holds an electrostatic latent image) is formed in a layer and is placed in contact with or in close proximity to the member. The so-called contact development method, in which the material is developed by bringing it into direct contact with the material, is widely used. In this method, a metal roller with a coating layer (called a developing roller) is generally used as the toner conveying member, but such a developing roller requires various functions for contact development. 1. For example, if the electrostatic latent image holder combined with the developing roller is a rigid body such as a selenium photoreceptor, the developing roller must have: ■ a flexible coating layer so as to obtain the necessary developing nip, and ■ contact. The coating layer on the core metal must be uniform in order to obtain the desired development characteristics, and more importantly, the characteristics of the surface or near the surface of the developing roller must be , ■ Constantly and stably imparting the desired charge polarity and amount of charge to the toner, ■ Good releasability from the toner,
Toner does not film; ■ Appropriate surface roughness (several μm or less) to form a uniform thin toner layer; ■ Smoothness to reduce chattering due to frictional resistance during contact. (1) Abrasion resistance. Regarding (2), when toner filming occurs, the amount of toner charge changes, causing unevenness in the amount of toner adhering to the developing roller, and as a result, there is a problem that unevenness of images occurs.
これ等の要求に対して、現像ローラーの芯金用被覆材料
としては低硬度の弾性体、通常ゴムと呼ばれるもの、例
えば、ニトリル−ブタジェン−ゴム(NOR) 、エビ
ロクロルヒドリンゴム(ECO) 、アクリルゴム、ク
ロロプレンゴム等の有極性ゴムやシリコーンゴム、エチ
レン−プロピレンゴム、スチレン−ブタジェンゴムなど
の高抵抗ゴムにカーボン、金属等の導電性微粒子を分散
し、たちのが使用されて来た。In response to these demands, the coating material for the core metal of the developing roller is a low-hardness elastic material, usually called rubber, such as nitrile-butadiene-rubber (NOR), ebichlorohydrin rubber (ECO), Polar rubbers such as acrylic rubber and chloroprene rubber, and high-resistance rubbers such as silicone rubber, ethylene-propylene rubber, and styrene-butadiene rubber, in which conductive fine particles of carbon, metal, etc. are dispersed, have been used.
しかしこれらの被覆材料を用いた従来の現像ローラーは
前述の要求、特に表面特性に関する(担以下の項目を満
足することは困難であった。However, it has been difficult for conventional developing rollers using these coated materials to satisfy the above-mentioned requirements, particularly regarding surface properties.
これは低硬度のゴムになるに従かい表面研磨性が悪くな
り、現像ローラーとして必要な表面粗さ(Rz)に仕上
げるのが困難であること、表面粘着性があるために当接
部材との摩擦抵抗性が大きいこと、ゴム強度としても胞
弱であるために非常に摩耗し易いこと、トナーの離型性
が悪いこと等によるものである。This is because the surface abrasiveness deteriorates as the hardness of the rubber decreases, making it difficult to finish the surface to the required surface roughness (Rz) for a developing roller, and because the surface is sticky, it is difficult to polish the surface with the contact member. This is due to the fact that it has high friction resistance, has low rubber strength and is therefore very easy to wear, and has poor toner releasability.
なお現像ローラーの酌記要求項目、特に■以下の項目は
トナーとも密接な関係があるので、トナーの面からの改
良も望まれていた。Note that the required items for the developing roller, especially the items listed below (1), are closely related to the toner, so improvements from the toner perspective were also desired.
七−均一
本発明の目的は非磁性1成分系1−ナーを用いる接触現
像法において1ヘナ一搬送部材と共にトナーを改良する
ことにより前記部材に要求される全ての機能項目、特に
表面特性に関する項目を満足し、従って常に安定して高
品質の画像を形成できる静電潜像の現像方法を提供する
ことである。7-Uniformity The purpose of the present invention is to improve the toner in contact development using a non-magnetic one-component 1-toner, together with the 1-henner and the conveying member, thereby achieving all the functional items required of the member, especially items related to surface properties. It is an object of the present invention to provide a method for developing an electrostatic latent image that satisfies the above requirements and can therefore consistently form high-quality images.
週−一」又
本発明方法はトナー搬送部材上に前記部材との摩擦によ
り所望極性に帯電させたトナーを薄層状に形成し、これ
を、前記部材と接するか。Week-1" Also, the method of the present invention involves forming a thin layer of toner charged to a desired polarity on a toner conveying member by friction with the member, and bringing this into contact with the member.
又は近接して配置された静電潜像保持体の潜像面に接触
させて静電潜像を現像する方法において、トナー搬送部
材として、支持体上に弾性体よりなる第一被覆層とその
上に可撓性樹脂及び導電性微粒子よりなる第二被覆層と
を設けたものを用い、且つトナーとして、着色樹脂粒子
を母体トナーとし、これにトナー搬送部材との摩擦によ
り母体トナーの帯電極性とは逆極性に帯電し得る微粒子
を添加した混合系を用いることを特徴とするものである
。Alternatively, in a method of developing an electrostatic latent image by bringing it into contact with the latent image surface of an electrostatic latent image holder disposed in close proximity, a first coating layer made of an elastic material on a support and its A second coating layer made of a flexible resin and conductive fine particles is provided on the toner, and colored resin particles are used as the base toner, and the charging polarity of the base toner is changed by friction with the toner conveying member. This is characterized by the use of a mixed system in which fine particles that can be charged to the opposite polarity are added.
まず本発明で用いられるトナー搬送部材について説明す
る。First, the toner conveying member used in the present invention will be explained.
本発明のトナー搬送部材は支持体上に第一被覆層と第二
被覆層とを設けることにより機能分離を計ったもので、
通常は従来と同様、ローラー状で用いられるが、ベルト
状で用いることもできる。The toner conveying member of the present invention is designed to separate functions by providing a first coating layer and a second coating layer on a support,
Usually, it is used in the form of a roller as in the past, but it can also be used in the form of a belt.
支持体としてはローラー状の場合は金属ローラーが、ま
たベルト状の場合はプラスチックフィルムや金属フィル
ム等が使用される。第−被覆層及び第二被rIIMに使
用される材料、形成法等は次の通りである。As the support, a metal roller is used in the case of a roller shape, and a plastic film, a metal film, etc. is used in the case of a belt shape. The materials, forming methods, etc. used for the first coating layer and the second coating layer are as follows.
第一被覆層について:
第一被覆層は従来のトナー搬送部材を構成していた弾性
体がいずれも使用できる。特に本発明に適する弾性体は
体積固有抵抗(ρ)が106〜10”Ω・amのいわゆ
る中抵抗領域にあるものが望ましい。ρのバラツキが少
ない安定な弾性体を形成するのに用いられるゴムとして
は、有極性ゴムであるニトリル−ブタジェンゴム(NB
R)、エピクロルヒドリンゴム(ECR)、アクリルゴ
ム。Regarding the first coating layer: For the first coating layer, any elastic body constituting a conventional toner conveying member can be used. In particular, it is desirable that the elastic body suitable for the present invention has a volume resistivity (ρ) in the so-called medium resistance region of 10 6 to 10”Ω・am.Rubber used to form a stable elastic body with little variation in ρ Nitrile-butadiene rubber (NB) is a polar rubber.
R), epichlorohydrin rubber (ECR), acrylic rubber.
クロロプレンゴム等があり、又、導電性微粒子としてカ
ーボンブラック、酸化金属粒子などを分散させたシリコ
ーンゴム、ウレタンゴム、エチレン−プロピレンゴム、
スチレン−ブタジェンゴム等も使用できるが、特にNB
R,ECR又はこれらの混合物が好ましい。ρの調整は
例えばNBRの場合はニトリル量の増減により、またN
BRとECRとの混合系の場合は混合比を変えることに
より容易に行なうことができる。勿論これらは低硬度、
耐摩耗性等実用上必要な性質を十分備えている。またN
BR−ECR混合混合湯合は耐オゾン性はNORより優
れているため、更に高信頼性の現像部材が得られる。There are chloroprene rubbers, silicone rubbers, urethane rubbers, ethylene-propylene rubbers, etc. in which conductive fine particles such as carbon black and metal oxide particles are dispersed.
Styrene-butadiene rubber etc. can also be used, but especially NB
R, ECR or mixtures thereof are preferred. For example, in the case of NBR, ρ can be adjusted by increasing or decreasing the amount of nitrile, or by changing the amount of NBR.
In the case of a mixed system of BR and ECR, this can be easily done by changing the mixing ratio. Of course these have low hardness,
It has sufficient properties necessary for practical use, such as wear resistance. Also N
Since the BR-ECR mixture has better ozone resistance than NOR, a developing member with higher reliability can be obtained.
なお第−被rlI層の厚さは0.5〜10mm程度が適
当である。また第一被覆層の形成方法は一般に支持体と
してローラーを用いた場合は弾性体をプレス成形、スチ
ーム成形等の成形法により、また支持体としてフィルム
を用いた場合は弾性体を適当な溶媒に溶解し、これをデ
ィッピング法、スプレー法等の塗布法により夫々、支持
体上に所望の厚さに成膜するというものである。Note that the thickness of the first rlI layer is suitably about 0.5 to 10 mm. In addition, the first coating layer is generally formed by forming the elastic body by press molding, steam molding, etc. when a roller is used as the support, or by dissolving the elastic body in an appropriate solvent when using a film as the support. The solution is dissolved and formed into a film to a desired thickness on a support by a coating method such as a dipping method or a spray method.
第二被rI1層について:
トナー搬送部材の表面層であり、トナーと接触する居で
あるからトナーに対して離型性が良く、体積固有抵抗ρ
が弾性体層と同レベルの10’〜1011Ω・Cmで、
可撓性を有する厚さ5〜60μm、特に30〜50μm
の合成樹脂層が好ましい。Regarding the second rI1 layer: It is the surface layer of the toner conveying member and is in contact with the toner, so it has good releasability with respect to the toner, and has a volume resistivity ρ.
is 10' to 1011 Ω・Cm, which is the same level as the elastic layer,
Flexible thickness 5-60 μm, especially 30-50 μm
The synthetic resin layer is preferred.
また、この樹脂の伸びは10〜500%、特に30〜3
00%のものが好ましい。10%以下の場合には低硬度
弾性体との追随性がなくなり、トナー搬送部材圧縮時に
割れなどが発生する原因となるし、500%以上の場合
は研磨性が悪くなるため所望の表面粗さが得られない。In addition, the elongation of this resin is 10 to 500%, especially 30 to 3
00% is preferable. If it is less than 10%, it will not be able to follow the low hardness elastic body, causing cracks to occur when compressing the toner conveying member, and if it is more than 500%, the polishing properties will be poor, so the desired surface roughness cannot be achieved. is not obtained.
又、樹脂層の厚さが10μm以下、特に5μm以下にな
ると、第一被覆層の弾性体の影響が強く現われ、又樹脂
層の厚さのバラツキが相対的に大きくなり好ましくない
。一方、厚さが60μmを超えると、第−被rIimの
プラス効果が薄くなるので好ましくない。いずれにして
も樹脂層の厚さは、選択された樹脂の電気的特性(一般
に高体積固有抵抗のものほど薄くてよい)や摩耗性の高
いものほど薄くてよい)などの性質および第一被覆層と
のバランスを総合して決定する。Furthermore, if the thickness of the resin layer is less than 10 μm, especially less than 5 μm, the influence of the elastic material of the first coating layer will be strong, and the variation in the thickness of the resin layer will become relatively large, which is not preferable. On the other hand, if the thickness exceeds 60 .mu.m, the positive effect of the first layer will be reduced, which is not preferable. In any case, the thickness of the resin layer depends on the electrical properties of the selected resin (in general, the higher the volume resistivity, the thinner the resin is), the more abrasive the resin, the thinner the resin, etc., and the first coating. Determine the overall balance with the layers.
第二被覆層として前述のごとき望ましい性質を備えた合
成樹脂としてはシリコーン樹脂、ウレタン樹脂、弗素樹
脂、変性弗素樹脂等を挙げることができる。これらの樹
脂を中抵抗とするためには、導電性材料としてカーボン
ブラック、各種金属微粒子などが添加されるが、前記合
成樹脂の性質をできるだけ維持して中抵抗化するために
、導電性材料の添加量はできるだけ少ない方が望ましく
、それにはカーボンブラックが好ましい。Examples of synthetic resins having the above-mentioned desirable properties for the second coating layer include silicone resins, urethane resins, fluororesins, modified fluororesins, and the like. In order to make these resins medium resistance, carbon black, various metal fine particles, etc. are added as conductive materials, but in order to maintain the properties of the synthetic resin as much as possible and make them medium resistance, conductive materials are added. It is desirable that the amount added be as small as possible, and carbon black is preferred for this purpose.
第二被覆層の形成方法は一般に前記樹脂と導電性微粒子
とを適当な溶媒、ボールミル、サンドミルなどの分散機
で分散し、必要に応じて溶媒で塗布液の粘度を調整した
後、これをスプレー法、ディッピング法などの塗布法に
より第一被覆層上に所望の厚さに成膜するというもので
ある。Generally, the second coating layer is formed by dispersing the resin and conductive particles in an appropriate solvent using a dispersing machine such as a ball mill or sand mill, adjusting the viscosity of the coating liquid with a solvent as necessary, and then spraying the coating liquid. A film is formed to a desired thickness on the first coating layer by a coating method such as a coating method or a dipping method.
この場合必要に応じて第一被覆層と第二被覆層との間に
適当なプライマーを使用して、これら階間をいっそう強
固に接着してもよい。In this case, if necessary, a suitable primer may be used between the first coating layer and the second coating layer to further firmly bond these layers.
なお前記塗布液により形成される第二被rI1.層にお
いてはρのバラツキが生じることがあるが、このような
問題は塗布時の塗布液の撹拌を十分に行なって均一な分
散液の状態で塗布を行なえば容易に解決できる。Note that the second coat rI1. formed by the coating liquid. Variations in ρ may occur in the layers, but such problems can be easily solved by sufficiently stirring the coating solution during coating and coating in a uniform dispersion state.
次に以上のようなトナー搬送部材と共に使用されるトナ
ーについて説明する。Next, toner used with the above-described toner conveying member will be explained.
本発明のトナーは接触現像において要求される性能とし
てトナー搬送部材上に凝集、塊等を生じることなくスム
ースに供給され、この部材との摩擦によって適切な帯電
量で所望極性に帯電し、且つ前記部材上に均一、且つ容
易に薄膜を形成し得ること(トナー薄層は一般にブレー
ドのようなトナー薄層形成部材によって形成される。)
が挙げられる。しかし従来の一般的な着色樹脂粒子より
なるトナーではこれらの要求を全て満足rることはでき
ず、供給時、特に環境変化や繰返し使用により凝集や塊
を生じるなど搬送性が悪く、またこのため均一な薄層を
形成することも困難であり、その結果、トナー搬送部材
の性能とも相まって残像や画像濃度ムラを発生し、鮮明
な画像を得ることば困難であった。そこで本発明者らは
種々検討の結果、通常の着色樹脂粒子を母体トナーとし
、これにトナー搬送部材との摩擦によりこの母体トナー
の71F電極性とは逆極性に帯電し得る微粒子を添加し
た混合系を用いると、母体トナーの流動性が改善される
結果、供給時、凝集等が起こらず、このため搬送性も向
上することが判明した。The toner of the present invention has the performance required in contact development: it is smoothly supplied onto the toner conveying member without causing agglomeration, lumps, etc., it is charged to a desired polarity with an appropriate amount of charge by friction with this member, and A thin film can be uniformly and easily formed on the member (the toner thin layer is generally formed by a toner thin layer forming member such as a blade).
can be mentioned. However, conventional toner made of general colored resin particles cannot satisfy all of these requirements, and has poor transportability, such as agglomeration and lumps during supply, especially due to environmental changes or repeated use. It is also difficult to form a uniform thin layer, and as a result, combined with the performance of the toner conveying member, residual images and uneven image density occur, making it difficult to obtain clear images. As a result of various studies, the inventors of the present invention found that a mixture was prepared in which normal colored resin particles were used as a base toner, and fine particles that could be charged to a polarity opposite to the 71F polarity of the base toner by friction with a toner conveying member were added. It has been found that when this system is used, the fluidity of the base toner is improved, and as a result, aggregation does not occur during supply, and therefore the transportability is also improved.
以上のような混合系トナーの一方の成分である母体トナ
ーは従来の一般的なトナーである着色樹脂粒子からなっ
ている。この着色樹脂粒子は結着樹脂、着色剤及び必要
あれば極性制御剤を溶融混練し、混練物を粉砕し、適当
な粒度に分級することにより作られる。こ\で結着樹脂
としては、ポリスチレン、クロロポリスチレン、ポリ−
α−メチルスチレン、スチレン−クロロスチレン共重合
体、スチレン−プロピレン共重合体、スチレン−ブタジ
ェン共重合体、スチレン−塩化ビニル共重合体、スチレ
ン−酢酸ビニル共重合体、スチレン−マレイン酸共重合
体、スチレン−アクリル酸エステル共重合体(スチレン
−アクリル酸メチル共重合体、スチレン−アクリル酸エ
チル共重合体、スチレン−アクリル酸ブチル共重合体、
スチレン−アクリル酸オクチル共重合体、スチレン−ア
クリル酸フェニル共重合体等)、スチレン−メタクリル
酸エステル共重合体(スチレン−メタクリル酸メチル共
重合体。The base toner, which is one component of the mixed toner described above, is made of colored resin particles, which is a conventional general toner. The colored resin particles are produced by melt-kneading a binder resin, a colorant and, if necessary, a polarity control agent, pulverizing the kneaded material, and classifying it into an appropriate particle size. The binder resin used here is polystyrene, chloropolystyrene, and polystyrene.
α-methylstyrene, styrene-chlorostyrene copolymer, styrene-propylene copolymer, styrene-butadiene copolymer, styrene-vinyl chloride copolymer, styrene-vinyl acetate copolymer, styrene-maleic acid copolymer , styrene-acrylic acid ester copolymer (styrene-methyl acrylate copolymer, styrene-ethyl acrylate copolymer, styrene-butyl acrylate copolymer,
Styrene-octyl acrylate copolymer, styrene-phenyl acrylate copolymer, etc.), styrene-methacrylate ester copolymer (styrene-methyl methacrylate copolymer).
スチレン−メタクリル酸エチル共重合体、スチレン−メ
タクリル酸ブチル共重合体、スチレン−メタグリル酸フ
ェニル共重合体等)、スチレン−α−クロルアクリル酸
メチル共重合体、スチレン−アクリロニトリル−アクリ
ル酸エステル共重合体等のスチレン系樹脂(スチレン又
はスチレン置換体を含む単一重合体又は共重合体)、塩
化ビニル樹脂、ロジン変性マレイン酸樹脂、フェノール
樹脂、エポキシ樹脂、ポリエステル樹脂、低分子量ポリ
エチレン、低分子量ポリプロピレン、アイオノマー樹脂
、ポリウレタン樹脂、ケトン樹脂、エチレン−エチルア
クリレート共重合体、キシレン樹脂、ポリビニルブチラ
ール等及びそれらの混合物が挙げられる。Styrene-ethyl methacrylate copolymer, styrene-butyl methacrylate copolymer, styrene-phenyl methacrylate copolymer, etc.), styrene-α-methyl chloroacrylate copolymer, styrene-acrylonitrile-acrylic acid ester copolymer Styrenic resins such as polymers (unipolymers or copolymers containing styrene or styrene substitutes), vinyl chloride resins, rosin-modified maleic acid resins, phenolic resins, epoxy resins, polyester resins, low molecular weight polyethylene, low molecular weight polypropylene, Examples include ionomer resins, polyurethane resins, ketone resins, ethylene-ethyl acrylate copolymers, xylene resins, polyvinyl butyral, and mixtures thereof.
着色剤としてはカーボンブラック、各種染料及び顔料が
挙げられる。Coloring agents include carbon black, various dyes, and pigments.
また極性制御剤としては正極性用として第4級アンモニ
ウム化合物、アミノ基含有ポリマー等が、また負極性用
としてサリチル酸金属塩等が挙げられる。Examples of polarity control agents include quaternary ammonium compounds and amino group-containing polymers for positive polarity, and salicylic acid metal salts for negative polarity.
その他、母体トナーにはトナーの熱特性、電気特性、物
理特性等を調整する目的で各種の可塑剤(フタル酸ジブ
チル、フタル酸ジオクチル等)、抵抗調整剤(酸化錫、
酸化鉛、酸化アンチモン等)等の助剤を添加することも
可能である。In addition, the base toner contains various plasticizers (dibutyl phthalate, dioctyl phthalate, etc.) and resistance adjusters (tin oxide,
It is also possible to add auxiliary agents such as lead oxide, antimony oxide, etc.).
混合系トナーの他方の成分である添加用微粒子としては
一般に流動性向上剤、研磨剤、又は潤滑剤として知られ
るSin、、TiO2、An20.、CeO,SiC,
ステアリン酸亜鉛等が使用される。これら添加用微粒子
の添加量はトナー搬送部材上のトナー薄層と潜像保持体
とが接触する現像領域においてこの微粒子が1×10−
4〜5 X 1O−2B/cm2の存在量になるように
調整することが好ましい。この存在量がlXl0−’m
g/cm2未満ではトナー搬送部材から潜像保持体への
トナーの移動効率(現像効率)が悪く、画像濃度の低い
、コントラストのない画像となるし、逆に存在量が5
X 10−2mg/c+n′を越えると、画像濃度は充
分であるが、カブリ、地肌汚れ等を発生することがある
。The additive fine particles that are the other component of the mixed toner include Sin, TiO2, An20. , CeO, SiC,
Zinc stearate and the like are used. The amount of these additive particles added is 1 x 10-
It is preferable to adjust the amount to be 4 to 5 X 1O-2B/cm2. This abundance is lXl0−'m
If the amount is less than 5 g/cm2, the toner transfer efficiency (development efficiency) from the toner transport member to the latent image holding member is poor, resulting in an image with low image density and no contrast.
If it exceeds X 10-2 mg/c+n', the image density is sufficient, but fogging, background stains, etc. may occur.
次に本発明で用いられるトナー搬送部材として現像ロー
ラーの製造例を以下に示す。Next, an example of manufacturing a developing roller as a toner conveying member used in the present invention will be shown below.
(以下余白)
(1)第一被覆層の形成例
表−1
月収(1)B)
表−1の配合割合で各々二本ロールを用いて均一になる
ように混練した後、上記条件で1次加硫し、8mmφの
芯金ローラー」二に弾性層の厚さGvn、ローラー外径
20mmに成形し、その後150°Cで4時間2次加硫
した。この成形ローラーの体積固有抵抗、ゴム硬度も表
−1中に示した。体積固有抵抗及びゴム硬度の測定法は
次の通りである。(Left below) (1) Example table for forming the first coating layer - 1 Monthly income (1) B) After kneading each mixture uniformly using two rolls at the mixing ratio shown in Table 1, The material was then vulcanized and formed into an 8 mm diameter cored roller with an elastic layer thickness Gvn and a roller outer diameter of 20 mm, followed by secondary vulcanization at 150° C. for 4 hours. The volume resistivity and rubber hardness of this forming roller are also shown in Table-1. The method for measuring volume resistivity and rubber hardness is as follows.
体積固有抵抗の測定は試料のローラーを20℃、60S
RI+の環境中に16時間放置した後、グー21社エレ
クトロメーター6100を用いて行なう。測定時の電極
は10mm幅の銅箔テープ(3M社テープNo、124
5)を用いて主電極とガード電極間距離を1mmとする
。To measure the volume resistivity, the sample roller was heated at 20°C for 60S.
After being left in an RI+ environment for 16 hours, the test was carried out using a Goo 21 Electrometer 6100. The electrode during measurement was a 10 mm wide copper foil tape (3M tape No. 124).
5), the distance between the main electrode and the guard electrode is set to 1 mm.
またゴム硬度の測定は加硫ゴム物理試験方法JIS K
6301に準じて行なう。Rubber hardness can also be measured using the vulcanized rubber physical test method JIS K.
6301.
(以下余白) (2)第二被覆層の形成例 表−2 (配合単位連部1!り 料の配合を表−3に示す。(Margin below) (2) Formation example of second coating layer Table-2 (Blending unit part 1! The composition of the ingredients is shown in Table 3.
表−3
上記配合物をボールミルで分散し、各々マスターバッチ
を作成した。なお、カーボンブラックとしてはBlac
k Pearls L (キャボット社)を使用した。Table 3 The above formulations were dispersed in a ball mill to create masterbatches. In addition, as carbon black, Black
K Pearls L (Cabot) was used.
この種類の異なるマスターバッチを基に主剤及び硬化剤
を添加してカーボンブラック/樹脂固型分= F/R比
を0.10に調整した。得られた塗注)溶媒(a)トル
エン
キシレン
(b)トルエン
酢酸エチル
50wt%
50すt%
39、Oすt%
17.5wt%
酢酸ブチル 17.5wt%エチ
ルセロソルブアセテート 17.5wt%メチルイ
ソブチルケトン 3.ht%キシレン
2.6%it%シクロヘキサン
2.0讐t%(C)キシレン
100讐t%第二被覆層の形成は第一被覆
層上に第二被覆層用塗料をスプレー塗布し、100℃で
2時間乾燥硬化させることにより行なった。なお第二被
覆層の厚さは30μmである。Based on these different types of masterbatches, a main agent and a curing agent were added to adjust the carbon black/resin solid content = F/R ratio to 0.10. Obtained coating) Solvent (a) Toluene xylene (b) Toluene Ethyl acetate 50wt% 50st% 39,Ost% 17.5wt% Butyl acetate 17.5wt% Ethyl cellosolve acetate 17.5wt% Methyl isobutyl ketone 3. ht% xylene
2.6%it% cyclohexane
2.0% (C) xylene
The 100% second coating layer was formed by spray coating the second coating layer coating on the first coating layer and drying and curing at 100° C. for 2 hours. Note that the thickness of the second coating layer is 30 μm.
以下に本発明方法を実施例によって説明する。The method of the present invention will be explained below using examples.
実施例1
低分子量ポリプロピレン 5 nサリチル酸
亜鉛塩 3
を熱ロールミルで加熱混練し、これを冷却後、ハンマー
ミルを用いて粗粉砕し、次いでエアージェット方式によ
る微粉砕機で微粉砕して、得られた微粉末を分級して平
均粒径10μmの母体トナーとした。この母体l・ナー
をトナー搬送部材上で薄層化した時の帯電量(以下、搬
送部材上の07Mという)は−14,2μc/gであっ
た。次にこの母体トナーに対し搬送部材上の07Mが+
2.5μc/gの酸化チタン微粒子を現像領域での存在
量が1 、5 X 10”’ mg/cm2になるよう
に添加し、本発明の混合系トナーを得た。なお母体トナ
ー及び添加用微粒子の帯電量(07M)測定法は次の通
りである。即ちトナー搬送部材上の薄層化したトナーを
第1図に示すような内部にフィルター10を有する金属
製吸引セルll付き金屈製吸引装匝の吸引口12から吸
引し、吸引セル後端に捕集されたトナーの重量M及び吸
引時に流れた電気量Qをクーロンメーター13で謂定し
、07Mを算出する。Example 1 Low molecular weight polypropylene 5 n salicylic acid zinc salt 3 was heated and kneaded in a heated roll mill, cooled, coarsely ground using a hammer mill, and then finely ground using an air jet type pulverizer to obtain a product. The fine powder obtained was classified to obtain a base toner having an average particle size of 10 μm. When this base l.toner was formed into a thin layer on a toner transport member, the amount of charge (hereinafter referred to as 07M on the transport member) was −14.2 μc/g. Next, 07M on the conveying member is + for this base toner.
Titanium oxide fine particles of 2.5 μc/g were added so that the amount present in the development area was 1.5 x 10'' mg/cm2 to obtain the mixed toner of the present invention. The method for measuring the charge amount (07M) of fine particles is as follows.That is, the thin layer of toner on a toner conveying member is transferred to a metal suction cell with a filter 10 inside as shown in FIG. The weight M of the toner sucked from the suction port 12 of the suction mount and collected at the rear end of the suction cell and the amount of electricity Q flowing during suction are determined using a coulomb meter 13, and 07M is calculated.
一方、表−1の配合1で作成した第−被覆層及びマスタ
ーバッチとして表−2の配合1を用いて表−3の具体例
1で作成した第二被覆層を有する現像ローラーを第2図
の接触現像装置〔図中1は静電潜像保持体(こぎでは電
子写真感光体)2はトナー搬送部材(こNでは現像ロー
ラー)、3はトナー層厚規制部材、4はトナー供給部材
、5は撹拌羽根、6はトナー、7はトナータンク〕にセ
ットし、これに前記混合系トナーを供給し、常温常湿下
、現像領域での添加用微粒子の存在量が1.5X 10
−’mg/am2という条件で電子写真感光体上の静電
潜像を現像した。On the other hand, FIG. 2 shows a developing roller having a second coating layer prepared according to Example 1 shown in Table 3 using Formulation 1 shown in Table 2 as a master batch and a second coating layer prepared according to Formulation 1 shown in Table 1. [In the figure, 1 is an electrostatic latent image holding member (electrophotographic photoreceptor in this case), 2 is a toner conveying member (developing roller in this case), 3 is a toner layer thickness regulating member, 4 is a toner supplying member, 5 is a stirring blade, 6 is a toner, and 7 is a toner tank], the mixed toner is supplied thereto, and the amount of additive fine particles in the development area is 1.5X 10 at room temperature and normal humidity.
The electrostatic latent image on the electrophotographic photoreceptor was developed under the conditions of -'mg/am2.
次に得られた画像を普通紙上に転写し、熱ローラーで定
着したところ、鮮明なコピー画像が得られた。更に10
000枚連続コピーしたが、画像品質は初期と変らず、
鮮明であった。The resulting image was then transferred onto plain paper and fixed using a heated roller, resulting in a clear copy image. 10 more
I made 000 copies in a row, but the image quality remained the same as the initial one.
It was clear.
また10℃−15%R)1及び30℃−90%R)lの
両環境下においても鮮明なコピー画像が得られた。Further, clear copy images were obtained under both environments of 10° C.-15% R)1 and 30° C.-90% R)1.
なお第2図のような接触現像法を更に詳しく説明すると
、トナータンク7に内臓されているトナー(二\では混
合系トナー)6は撹拌羽根5により、トナー供給部材4
に強制的に寄せられ、トナー供給部材4に供給される。To explain in more detail the contact development method as shown in FIG.
The toner is forcibly brought to the toner supply member 4 and supplied to the toner supply member 4.
そして、トナー供給部材4に取り込まれたトナーは、ト
ナー供給部材が矢印方向に強く回転することによりトナ
ー搬送部材2に運ばれて摩擦され、こ\で静電的、ある
いは物理的に吸着され、ついでトナー搬送部材2の回転
及びトナー層厚規制部材3により前記搬送部材上に均一
なトナー薄層が形成されると共に摩擦帯電する。その後
、トナー搬送部材2と接触もしくは近接して配置された
静電潜像保持体1の潜像面に運ばれ、これとトナー7I
mとが接触することにより静電潜像が現像される。Then, the toner taken into the toner supply member 4 is conveyed to the toner conveyance member 2 by strong rotation of the toner supply member in the direction of the arrow, and is rubbed by the toner conveyance member 2, where it is electrostatically or physically attracted. Then, by rotating the toner conveying member 2 and toner layer thickness regulating member 3, a uniform thin layer of toner is formed on the conveying member and frictionally charged. Thereafter, the toner is transported to the latent image surface of the electrostatic latent image holding member 1 that is placed in contact with or in close proximity to the toner conveying member 2, and the toner 7I
The electrostatic latent image is developed by the contact with m.
実施例2
低分子量ポリプロピレン 5 n含金属錯体
4 nを用いて実施例1と同
様に母体トナーを作成した。この母体トナーの搬送部材
上の07Mは−12,1μc/gであった。この母体ト
ナーに対し、搬送部材上の07Mが+7.5μc/gの
酸化アルミニウム微粒子を現像領域での存在量がIlX
lo−3ffi/am2になるように添加し、本発明の
混合系トナーを得た。Example 2 A base toner was prepared in the same manner as in Example 1 using 5 n of low molecular weight polypropylene and 4 n of metal-containing complex. The 07M of this base toner on the conveying member was -12.1 μc/g. With respect to this base toner, aluminum oxide fine particles with 07M of +7.5 μc/g on the conveying member are added in an amount of IlX in the development area.
The mixture was added to give lo-3ffi/am2 to obtain the mixed toner of the present invention.
次に表−1の配合2を用いて作成した第−被覆層及び表
−2の配合2のマスターバッチを用いて表−3の具体例
2で作成した第二被覆層を有する現像ローラーを第1図
の現像装置にセットし、引続き前記混合トナーをこの装
置に供給し、以下、現像領域での添加用微粒子の存在量
をIX 1.0−’mg/cm2とした他は実施例1と
同様に常温常湿下で連続コピーを行なったところ、初期
も10000枚コピー後も鮮明なコピーが得られた。Next, a developing roller having a second coating layer prepared using Formulation 2 of Table 1 and a second coating layer prepared according to Specific Example 2 of Table 3 using the masterbatch of Formulation 2 of Table 2 was applied. The mixed toner was then set in the developing device shown in FIG. 1, and the mixed toner was subsequently supplied to this device. Similarly, when continuous copying was performed at room temperature and humidity, clear copies were obtained both at the initial stage and after copying 10,000 copies.
更に10℃−15%R)I及び30℃−90%RHの両
環境下においても鮮明な画像が得られた。Furthermore, clear images were obtained under both environments of 10° C.-15% R)I and 30° C.-90% RH.
実施例3
低分子量ポリプロピレン 5 〃サリチル酸亜
鉛華 3 〃カーボンブラック
(C#44、三菱カーボン製) 6 〃を用いて実施
例1と同様にして母体トナーを作成した。この母体トナ
ーの搬送部材上のQ/Mは−15,0μc/gであった
。次にこの母体トナーに対し、搬送部材上のQ/Mが+
16.5μc/gのステアリン酸亜鉛微粒子を現像領域
での存在量が5 X 10−4mg/Cm2となるよう
に添加して本発明の混合系トナーを得た。Example 3 A base toner was prepared in the same manner as in Example 1 using 5 low molecular weight polypropylene, 3 zinc white salicylate, and 6 carbon black (C#44, manufactured by Mitsubishi Carbon). The Q/M of this base toner on the conveying member was -15.0 μc/g. Next, for this base toner, Q/M on the conveying member is +
A mixed toner of the present invention was obtained by adding 16.5 .mu.c/g of fine zinc stearate particles in an amount of 5.times.10@-4 mg/Cm2 in the development area.
次に表−1の配合3を用いて作成した第−被覆層及び表
−2の配合3のマスターバッチを用いて表−3の具体例
3で作成した第二被覆層を有する現像ローラーを第1図
の現像装置にセットし、引続き前記混合トナーをこの装
置に供給し、以下、現像領域での添加用微粒子の存在量
を5 X 10−’mg/am”とした他は実施例1と
同様に常温常湿下で連続コピーを行なったところ、初期
も10000枚コピー後も鮮明なコピーが得られた。Next, a developing roller having a first coating layer prepared using Formulation 3 of Table 1 and a second coating layer prepared according to Example 3 of Table 3 using the masterbatch of Formulation 3 of Table 2 was applied. The mixed toner was then set in the developing device shown in FIG. Similarly, when continuous copying was performed at room temperature and humidity, clear copies were obtained both at the initial stage and after copying 10,000 copies.
更に10℃−15%11+1及び30℃−90%RHの
両環境下においても鮮明な画像が得られた。Furthermore, clear images were obtained under both environments of 10° C.-15% 11+1 and 30° C.-90% RH.
実施例4
サルチル酸亜鉛塩の代りに、ニグロシン系染料を使用し
た他は実施例1と同じ方法で混合系トナーを作成した。Example 4 A mixed toner was prepared in the same manner as in Example 1 except that nigrosine dye was used instead of zinc salicylate.
この混合系トナーの搬送部材上のQ/Mは+13,1μ
c/gであった6次にこの母体トナーに対し、搬送部材
上のQ/Mが−20,0μc/gの酸化珪素微粒子を、
現像領域での存在量がI X 10−3mg/am”に
なるように添加し、本発明の混合系トナーを得た。The Q/M of this mixed toner on the conveying member is +13.1μ
6 Next, silicon oxide fine particles with a Q/M of -20.0 μc/g on the conveying member were added to this base toner, which had a Q/M of -20.0 μc/g.
It was added so that the amount present in the development area was I x 10-3 mg/am'' to obtain the mixed toner of the present invention.
次に実施例1で用いた現像ローラーを第1図の装置にセ
ットし、更に感光体上の潜像の電荷極性を実施例1とは
逆にした後、前記混合トナーをこの装置に供給し、以下
、現像領域での添加用微粒子の存在量をl X 10−
3mg/cm2とした他は実施例1と同様に常温常湿下
で連続コピーを行なったところ、初期も10000枚コ
ピー後も鮮明なコピーが得られた。Next, the developing roller used in Example 1 was set in the apparatus shown in FIG. 1, and after the charge polarity of the latent image on the photoreceptor was reversed from that in Example 1, the mixed toner was supplied to this apparatus. , hereinafter, the amount of additive fine particles present in the development area is expressed as l x 10-
Continuous copying was performed at normal temperature and normal humidity in the same manner as in Example 1 except that the concentration was 3 mg/cm2, and clear copies were obtained both at the initial stage and after copying 10,000 copies.
更に10℃−15%RH及び30℃−90%R11の両
環境下においても鮮明な画像が得られた。Furthermore, clear images were obtained under both environments of 10° C.-15% RH and 30° C.-90% R11.
比較例1
表−1の配合lを用いて作成した第−被覆層及び表−3
の具体例1からマスターバッチを除いた処方(従ってカ
ーボンブラックも含まず)を用いて作成した第二被覆層
を有する現像ローラーを用いた他は実施例1と同じ方法
で現像を行なったところ、常温常湿下では鮮明な画像が
得られたが、10℃−15%R+1の環境下ではコピー
画像に地肌部へのトナー付着による汚れが見られた。Comparative Example 1 The first coating layer created using the formulation 1 in Table 1 and Table 3
Development was carried out in the same manner as in Example 1, except for using a developing roller having a second coating layer prepared using the formulation from Specific Example 1 except for the masterbatch (therefore, it did not contain carbon black either). A clear image was obtained under normal temperature and normal humidity, but under an environment of 10° C.-15% R+1, stains due to toner adhesion to the background portion were observed in the copied image.
比較例2
混合系トナーの代りに母体1〜ナーを単独で用いた他は
実施例1と同じ方法で常温常湿下にコピーを行なったと
ころ、コピー初期は若干濃度の低い画像が得られたもの
の、10000枚コピー後は更に画像濃度は低下した。Comparative Example 2 Copying was performed at room temperature and humidity in the same manner as in Example 1 except that toner 1 to base 1 was used alone instead of the mixed toner, and an image with a slightly low density was obtained at the initial stage of copying. However, after copying 10,000 sheets, the image density further decreased.
比較例3
添加用微粒子として実施例4で使用した酸化ケイ素微粒
子を用いた他は実施例1と同じ方法で混合系トナーを作
り、以下、この混合系トナ−を用いて実施例1と同様に
して常温常湿下に現像を行なったところ、濃度の低い、
コントラストのない画像が得られた。Comparative Example 3 A mixed toner was prepared in the same manner as in Example 1 except that the silicon oxide fine particles used in Example 4 were used as the additive fine particles. When I developed it at room temperature and humidity, I found that the density was low.
An image with no contrast was obtained.
比較例4
実施例4で用いた母体トナーを用いた他は実施例1と同
じ方法で混合系トナーを作り、更に感光体上の潜像の電
荷極性を実施例1とは逆にした他は実施例1と同じ方法
で常温常湿下に現像を行なったところ、濃度の低い、コ
ントラストのない画像が得られた。Comparative Example 4 A mixed toner was prepared in the same manner as in Example 1 except that the base toner used in Example 4 was used, and the charge polarity of the latent image on the photoreceptor was reversed from Example 1. When development was carried out at room temperature and humidity in the same manner as in Example 1, an image with low density and no contrast was obtained.
実施例5
現像領域での添加用微粒子の存在量を5×10−5mg
/am2とした他は実施例1と同じ方法で常温常湿下に
連続コピーを行なったところ、コピー初期は若干濃度の
低い画像が得られ、また10000枚コピー後は更に若
干画像濃度が低下した。Example 5 The amount of additive fine particles in the development area was 5 x 10-5 mg.
When continuous copying was performed at room temperature and humidity in the same manner as in Example 1 except that /am2 was used, an image with slightly low density was obtained at the initial stage of copying, and the image density further decreased slightly after copying 10,000 sheets. .
実施例6
現像領域での添加用微粒子の存在量を8×10−”mg
/cm”とした他は実施例1と同じ方法で常温常湿下に
連続コピーを行なったところ、コピー初期は濃度の高い
鮮明な画像が得られたが、10000枚コピー後は若干
地肌汚れ及びカブリが発生した。Example 6 The amount of additive fine particles in the development area was set to 8×10-”mg
Continuous copying was performed at room temperature and humidity using the same method as in Example 1, except that the setting was 10,000 sheets. Fog occurred.
以下の結果を表−4に示す。The following results are shown in Table-4.
表−4
による。〕
勃−一一敦
以上の如く本発明方法は非磁性1成分系トナーを用いる
接触現像法においてトナー搬送部材と共にトナーを改良
することにより前記部材に要求される全ての機能項目、
特に表面特性に関する項目を満足し、従って常に安定し
て高品質の画像を形成することができる。According to Table-4. ] As described above, the method of the present invention improves the toner together with the toner conveying member in the contact development method using non-magnetic one-component toner, thereby achieving all the functional items required of the member,
In particular, it satisfies the requirements regarding surface properties, and therefore can consistently form high-quality images.
第1図は本発明方法で用いられる混合系トナーの各混合
成分の帯電量を測定するための装置図、第2図は実施例
で用いた接触現像装置の概略図である。
1:静電潜像担持体
2:トナー搬送部材
3:トナー層厚規制部材
4:トナー供給部材 5:撹拌羽根FIG. 1 is a diagram of a device for measuring the amount of charge of each mixed component of a mixed toner used in the method of the present invention, and FIG. 2 is a schematic diagram of a contact developing device used in Examples. 1: Electrostatic latent image carrier 2: Toner transport member 3: Toner layer thickness regulating member 4: Toner supply member 5: Stirring blade
Claims (1)
性に帯電させたトナーを薄層状に形成し、これを、前記
部材と接するか、又は近接して配置された静電潜像保持
体の潜像面に接触させて静電潜像を現像する方法におい
て、トナー搬送部材として、支持体上に弾性体よりなる
第一被覆層とその上に可撓性樹脂及び導電性微粒子より
なる第二被覆層とを設けたものを用い、且つトナーとし
て、着色樹脂粒子を母体トナーとし、これにトナー搬送
部材との摩擦により母体トナーの帯電極性とは逆極性に
帯電し得る微粒子を添加した混合系を用いることを特徴
とする静電潜像の現像方法。1. Form a thin layer of toner charged to a desired polarity by friction with the toner conveying member, and transfer this to an electrostatic latent image carrier disposed in contact with or close to the toner conveying member. In a method of developing an electrostatic latent image by bringing it into contact with a latent image surface, the toner conveying member includes a first coating layer made of an elastic material on a support and a second coating layer made of a flexible resin and conductive fine particles on the support. A mixed system in which colored resin particles are used as a base toner, and fine particles that can be charged to a polarity opposite to that of the base toner by friction with a toner conveying member are added. A method for developing an electrostatic latent image, characterized by using.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63143172A JP2895837B2 (en) | 1988-06-10 | 1988-06-10 | Method of developing electrostatic latent image |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63143172A JP2895837B2 (en) | 1988-06-10 | 1988-06-10 | Method of developing electrostatic latent image |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH021881A true JPH021881A (en) | 1990-01-08 |
| JP2895837B2 JP2895837B2 (en) | 1999-05-24 |
Family
ID=15332591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63143172A Expired - Lifetime JP2895837B2 (en) | 1988-06-10 | 1988-06-10 | Method of developing electrostatic latent image |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2895837B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04145448A (en) * | 1990-10-08 | 1992-05-19 | Tomoegawa Paper Co Ltd | Nonmagnetic one-component developing method |
| JPH1010784A (en) * | 1996-06-27 | 1998-01-16 | Brother Ind Ltd | Positively chargeable one-component developer and image forming apparatus using the developer |
| JP2000019835A (en) * | 1998-07-01 | 2000-01-21 | Mita Ind Co Ltd | Developing device and developing roller used therefor |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5888030B2 (en) | 2011-03-17 | 2016-03-16 | 株式会社リコー | Toner, developer, image forming apparatus, and process cartridge |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6227751A (en) * | 1985-07-29 | 1987-02-05 | Fuji Xerox Co Ltd | Developer for electrostatic latent image |
| JPS62223771A (en) * | 1986-03-26 | 1987-10-01 | Toshiba Corp | Developing device |
-
1988
- 1988-06-10 JP JP63143172A patent/JP2895837B2/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6227751A (en) * | 1985-07-29 | 1987-02-05 | Fuji Xerox Co Ltd | Developer for electrostatic latent image |
| JPS62223771A (en) * | 1986-03-26 | 1987-10-01 | Toshiba Corp | Developing device |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04145448A (en) * | 1990-10-08 | 1992-05-19 | Tomoegawa Paper Co Ltd | Nonmagnetic one-component developing method |
| JPH1010784A (en) * | 1996-06-27 | 1998-01-16 | Brother Ind Ltd | Positively chargeable one-component developer and image forming apparatus using the developer |
| JP2000019835A (en) * | 1998-07-01 | 2000-01-21 | Mita Ind Co Ltd | Developing device and developing roller used therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2895837B2 (en) | 1999-05-24 |
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