JPS59223459A - Carrier particle for developing electrostatic charge image - Google Patents

Carrier particle for developing electrostatic charge image

Info

Publication number
JPS59223459A
JPS59223459A JP58098809A JP9880983A JPS59223459A JP S59223459 A JPS59223459 A JP S59223459A JP 58098809 A JP58098809 A JP 58098809A JP 9880983 A JP9880983 A JP 9880983A JP S59223459 A JPS59223459 A JP S59223459A
Authority
JP
Japan
Prior art keywords
group
org
core material
particles
denotes
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
Application number
JP58098809A
Other languages
Japanese (ja)
Inventor
Takayoshi Aoki
孝義 青木
Yukihiro Ishii
石井 幸広
Koichi Tanaka
田中 公一
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Business Innovation Corp
Original Assignee
Fuji Xerox Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fuji Xerox Co Ltd filed Critical Fuji Xerox Co Ltd
Priority to JP58098809A priority Critical patent/JPS59223459A/en
Publication of JPS59223459A publication Critical patent/JPS59223459A/en
Pending legal-status Critical Current

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Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/10Developers with toner particles characterised by carrier particles
    • G03G9/113Developers with toner particles characterised by carrier particles having coatings applied thereto
    • G03G9/1138Non-macromolecular organic components of coatings

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  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Developing Agents For Electrophotography (AREA)

Abstract

PURPOSE:To enable electrostatic charging of a toner to positive and to decrease the change in the electric resistance of a core material by treating the surface of the core material with an org. silane compd. to form a coating layer of the org. silane compd. on the surface. CONSTITUTION:Carrier particles for developing an electrostatic charge image contains core particles and a coating layer of an org. silane compd. at least the terminal of which is perfluorinated. The org. silane compd. can be expressed by the general formula, in which A denotes an alkylene group, fluoroalkylene group, halogen subst. fluoroalkylene group, arylene group, fluoroarylene group or halogen subst. arylene group, B denotes an alkylene group, oxyalkylene group or polyoxyalkylene group, R denotes an alkyl group of 1-4 carbon atom and n denotes 1-3 positive integer. There are magnetic particles such as triiron tetroxide, gamma-iron sesquoxide, cobalt, etc. and particles, etc. dispersed with these magnetic particles in the binder resin as the core material. The amt. of the org. silane compd. to be used for coating is about 0.001-0.5pts.wt. by 100pts.wt. the core material.

Description

【発明の詳細な説明】 電潜像の現像のために使用される静電荷像現像用キャリ
ヤ粒子に関する。更に詳細にはコア粒子と被覆層とから
なる高耐久性を有する静電荷像現像用キャリヤ粒子に関
する。
DETAILED DESCRIPTION OF THE INVENTION This invention relates to electrostatic image development carrier particles used for the development of electrostatic latent images. More specifically, the present invention relates to carrier particles for developing electrostatic images having high durability and comprising core particles and a coating layer.

従来技術 電子写真法においては、セレンをはじめとする光導電性
物質を感光体として用い、これに種々の手段によシミ気
的潜像を形成し、この潜像に磁気ブラシ現像法等を用い
てトナーを付着、顕像化させる方式が一般的に採用され
ている。
In the conventional electrophotographic method, a photoconductive substance such as selenium is used as a photoreceptor, a spot-like latent image is formed on it by various means, and a magnetic brush development method or the like is applied to this latent image. Generally, a method is adopted in which toner is attached and visualized using a method.

この現像工程においては、トナーに適当量の正または負
の電荷を付与するために、キャリヤと呼ばれる担体粒子
が使用されている。キャリヤは大別するとコートキャリ
ヤと非コートキャリヤとに分類されるが、現像剤寿命等
を考慮すればコートキャリヤの方が優れており、実際に
各種の型のコートキャリヤが製造され実用化されている
In this development step, carrier particles called carriers are used to impart an appropriate amount of positive or negative charge to the toner. Carriers can be broadly classified into coated carriers and non-coated carriers, but coated carriers are superior in terms of developer life, etc., and various types of coated carriers have actually been manufactured and put into practical use. There is.

このコートキャリヤは種々の特性を有することが必要と
されるが、中でも特に重要な特性として適当な帯電性、
耐衝撃性、耐摩耗性、コア(芯物質)と被覆材料との良
好な密着性等を挙げることができる。
This coated carrier is required to have various properties, among which the most important properties are appropriate chargeability,
Examples include impact resistance, abrasion resistance, and good adhesion between the core (core material) and the coating material.

上記要求特性を考慮すると、従来使用されてきたコート
キャリヤは依然として改善すべき問題を残しており、完
全なものはいまのところ知られていない。例えばフッ素
化ビニルポリマー類は帯電性において優れているが、コ
アとの密着性において問題があり、またアクリル系ポリ
マー類は機械的強度、コアとの密着性の点では満足でき
るものノ、帯電性において問題があるとされている。い
ずれにしても、現状では一長一短のある被覆材料の使用
を余儀なくされている。特に、感光体として有機感光体
を用いる場合にはトナーを正に帯電′させる必要があり
、この帯電制御はキャリヤの被ぞσ材料を連室選択する
ことにょシ行なわれてきた。
Considering the above-mentioned required characteristics, the coat carriers used in the past still have problems to be improved, and no perfect one is known at present. For example, fluorinated vinyl polymers have excellent chargeability, but they have problems with adhesion to the core, and acrylic polymers are satisfactory in terms of mechanical strength and adhesion to the core, but have good chargeability. It is said that there is a problem with this. In any case, currently we are forced to use coating materials that have advantages and disadvantages. Particularly, when an organic photoreceptor is used as a photoreceptor, it is necessary to positively charge the toner, and this charging control has been carried out by selecting the carrier's σ material in a continuous manner.

このような目的で従来量も頻繁に使用されてきたものは
フッ素化ビニルポリマー類であった。しがしながら、前
述の如くフッ素化ビニルポリマー類はコアとの密着性に
劣り、かつ耐衝麹性においても問題がある。また、この
種の被覆を有するキャリヤは絶縁性が高く、エツジ効果
が顕著で、ソリッド濃度が極めて低いという欠点を有し
ている。
Fluorinated vinyl polymers have been frequently used in conventional amounts for such purposes. However, as mentioned above, fluorinated vinyl polymers have poor adhesion to the core and also have problems in impact resistance. Furthermore, carriers with this type of coating have the disadvantages of high insulation, pronounced edge effects, and extremely low solids concentration.

発明の目的 このような情況の下で本発明者等は上記従来法の難点を
改善すべく種々研究、検討の結果、特定のシラン化合物
で表面処理することにより所定の特性を示す静電荷像現
像用キャリヤ粒子を得ることが可能であることを見出し
た。
Purpose of the Invention Under these circumstances, the inventors of the present invention have conducted various studies and examinations in order to improve the drawbacks of the above-mentioned conventional methods.As a result, the present inventors have developed an electrostatic image development method that exhibits predetermined characteristics by surface treatment with a specific silane compound. We have found that it is possible to obtain carrier particles for

即ち、本発明の目的は負の帯電性に優れ、かつコアの電
気抵抗の変化の少ない被覆キャリヤを提供することにあ
る。
That is, an object of the present invention is to provide a coated carrier that has excellent negative chargeability and less change in the electrical resistance of the core.

本発明の前記並びにその他の目的は以下の記載から一層
明白となるであろう。
The above and other objects of the present invention will become more apparent from the following description.

発明の構成 本発明の前記目的はコア粒子と、少なくとも末端カバー
フロロ化された有機シラン化合物の被覆層とを含む静電
荷像現像用キャリヤ粒子によって達成することができる
DESCRIPTION OF THE INVENTION The above-mentioned objects of the present invention can be achieved by carrier particles for electrostatic image development comprising a core particle and a coating layer of at least a terminal cover fluorinated organosilane compound.

本発明において使用する前記有機72ン化合物ti以下
の一般式で表わすことができる。
The organic compound used in the present invention can be represented by the following general formula.

(CF 5− A −B セSt −6OR)A−n但
し、該一般式においてAはアルキレン基、フロロアルキ
レン基、ハロゲン置換フロ四フロ中レン基、了り−レン
基、70ロアリーレン基またはハロダン置換アリーレン
基を表わし、Bはアルキレン基、オキシアルキレン基ま
たはポリオキシアルキレン基であり、Rは炭素数/〜ケ
のアルキル基を表わし、nは/〜3の正の整数を表わす
(CF5-A-BSeSt-6OR)A-nHowever, in the general formula, A is an alkylene group, a fluoroalkylene group, a halogen-substituted fluorotetrafluorolene group, an arylene group, a 70roarylene group, or a halodane group. It represents a substituted arylene group, B is an alkylene group, oxyalkylene group or polyoxyalkylene group, R represents an alkyl group having 1 to 6 carbon atoms, and n represents a positive integer of 1 to 3 carbon atoms.

好ましくは前記アルキレンは炭素数/〜gのものであり
、またポリオキシアルキレンは−〜ざ個のオキシアルキ
レンを含むものである。
Preferably, the alkylene has carbon atoms/g, and the polyoxyalkylene contains - to g oxyalkylene.

上記の少なくとも末端がパーフロロ化された有機シラン
化合物の具体例としては’f−7や一7o。
Specific examples of the above-mentioned organic silane compounds perfluorinated at least at the terminal are 'f-7 and -7o.

プロピルプロピルトリメトキシシラン、  7−z4−
70ロブチルゾロピルトリメトキシシラン、r−ノや一
フロログロビルfロピルトリエトキシシラン、  γ−
パー70ロブチルプロピルトリエトキシシラン、  γ
−パー70ロヘキシル、プロビルトリメトキシシ2ン、
  γ−/4’ −71:I l:lオクチルグはピル
トリメトキシシラン、 γ−パー70ロヘー’F シA
/ 7’ロビルトリエトキシシラン、  γ−ノや一7
0ロオクチルプロビルトリエトキシシラン、δ−/p−
7oafロビルプチルトリメトキシシラン、 δ−パー
70ロゾチルブチルトリメトキシシラン、  δ−パー
フロロプロピルブチルトリエトキシ7ラン、  δ−パ
ー70ロブチルゾチルトリエトキシシラン、  ビス−
(γ−/’?−7oo7’ロビルプロピ/I/)ジメト
キシシラン、  ビス−(γ−)ぐ−70ロゾチ/L/
fロビル)ジメトキシシラン、  ビス−(r−79−
フロロブ、ロビルグロビル)ジェトキシシラン、 ビス
−(γ−パーフロofチルプpピル)ジェトキシシラン
、 r−パー70ロゾpポキシプロビルトリメトキシシ
ラン、r−ノや一70ロプトキシゾロビルトリメトキシ
シラン、  r−747四ログロポキシノVピルトリエ
トキシシラン、 γ−ノや一フロログトキシプロビルト
リエトキシシラン、  γ−パー70ロヘキシルオキシ
デロビルトリメトキシシラン、  γ−ノぐ一フロロオ
クチルオキシゾロピルトリメトキシシラン、  δ−ノ
ぐ一70ロゾロ−キシブチルトリメトキシシラン、 δ
−パー70ロブトキシブチルトリメトキシシラン、 δ
−パー70ロヘキシルオキシプチルトリメトキシシラン
、  δ−パー70ロオクチルオキシブチルトリメトキ
シシラン、ビス−(γ−パー70ロブトキシプロビル)
ジメトキシシラン、  ビス−(δ−パーフロロへキシ
ルオキシブチル)ジェトキシシラン等を咲けることがで
きる。これらは単独で、もしくは一種以上の組合せで使
用することができる。
Propylpropyltrimethoxysilane, 7-z4-
70 butylzolopyltrimethoxysilane, r-no-fluoroglobil f-ropyltriethoxysilane, γ-
Par70 butylpropyltriethoxysilane, γ
- Par70 lohexyl, proyl trimethoxycin,
γ-/4'-71:I l:l Octylg is pyrutrimethoxysilane, γ-par70Rohe'F Shea
/ 7'robiltriethoxysilane, γ-noyaichi 7
0-octylprobyltriethoxysilane, δ-/p-
7oaf lovir butyltrimethoxysilane, δ-per70 lozotylbutyltrimethoxysilane, δ-perfluoropropylbutyltriethoxy7rane, δ-per70 butylzotyltriethoxysilane, bis-
(γ-/'?-7oo7'rovirpropy/I/)dimethoxysilane, bis-(γ-)gu-70lozoti/L/
f-rovir) dimethoxysilane, bis-(r-79-
fluorob, robil globil) jetoxysilane, bis-(gamma-perflo of thirp pyl) jetoxysilane, r-per 70 poxyprobyl trimethoxysilane, r-perfluoro-70 poxypropyl trimethoxysilane, r-747 tetrachlorogropoxypropyltriethoxysilane, γ-propyrologoxypropyltriethoxysilane, γ-per70lohexyloxyderobyl trimethoxysilane, γ-propyrofluorooctyloxyzolopyltrimethoxysilane Silane, δ-Noguichi 70rozo-butyltrimethoxysilane, δ
-Par70 buttoxybutyltrimethoxysilane, δ
-Per70 lohexyloxybutyltrimethoxysilane, δ-per70 looctyloxybutyltrimethoxysilane, bis-(γ-per70 lobutoxyprobyl)
Dimethoxysilane, bis-(δ-perfluorohexyloxybutyl)jethoxysilane, etc. can be used. These can be used alone or in combination of one or more.

一方、本発明で使用するコア材料としては四三酸化鉄、
  r−三二酸化鉄、MnZnフェライト、・NiZn
フェライト、Haフェライ、ト、  二酸化クロム、 
 鉄、  ニッケル、  コバルト等の磁性粒子および
これら磁性粒子を結着樹脂に分散した粒子等を例示する
ことができ、通常−〇〜左o。
On the other hand, the core materials used in the present invention include triiron tetroxide,
r-iron sesquioxide, MnZn ferrite, NiZn
Ferrite, Ha ferrite, chromium dioxide,
Examples include magnetic particles of iron, nickel, cobalt, etc., and particles in which these magnetic particles are dispersed in a binder resin.

μm程度の大きさのものが使用される。A size of about μm is used.

本発明の静電荷像現像用キャリヤ粒子は前記の如きコア
材料を上記の有機シラン化合物で表面処理し、該コア材
料表面上に化学結合或いは吸着によシ有機シラン化合物
の被覆層を形成することによシ得ることができる。
The carrier particles for developing electrostatic images of the present invention can be obtained by surface-treating the core material as described above with the organic silane compound described above, and forming a coating layer of the organic silane compound on the surface of the core material by chemical bonding or adsorption. You can get good results.

コア材料の表面処理のためには、例えば前記シラン化合
物を適、当な溶媒に溶解し、得られる溶液中にコア材料
を浸漬し、しかる後に脱溶媒、乾燥、高温焼付けする方
法、或いはコア材料を流動化床中で浮遊させ、シラン化
合物を含む溶液を噴霧塗布し、乾燥、高温焼付けする方
法等を利用することができる。これら方法において、高
温焼付は処理は必ずしも必要とされないが、コア材料と
シラン化合物の被膜との密着強度を高めるという観点か
ら約70θ〜200ccでの高温処理を行うことが好ま
しい。
For surface treatment of the core material, for example, the silane compound is dissolved in an appropriate solvent, the core material is immersed in the resulting solution, and then the solvent is removed, dried, and baked at high temperature. A method can be used in which the material is suspended in a fluidized bed, a solution containing a silane compound is sprayed, dried, and baked at a high temperature. In these methods, high-temperature baking is not necessarily required, but from the viewpoint of increasing the adhesion strength between the core material and the silane compound coating, it is preferable to perform high-temperature baking at about 70 θ to 200 cc.

上記有機シラン化合物の溶媒としては、例えば11゜ アルコール類、ケトン類、トルエン等公知の溶媒が使用
できる。
As the solvent for the organic silane compound, known solvents such as 11° alcohols, ketones, and toluene can be used.

有機シラン化合物の被覆量は、通常コア材料100重骨
部に対しO0θθ/〜θ、3重量部程度であることが適
している。このためには、コア材料の%面処理において
使用するシラン化合物溶液の濃度はO0S〜/θwt係
程度であることが望ましい。
The amount of the organic silane compound coated is usually approximately 3 parts by weight, O0θθ/~θ, per 100 parts of the core material. For this purpose, it is desirable that the concentration of the silane compound solution used in the surface treatment of the core material is approximately O0S~/θwt.

かくして得られる本発明のキャリヤはトナーと混合して
、静電潜像の現像に使用される。トナーとしては、バイ
ンダー樹脂中に着色剤を分散させた微粒子であって、通
常電子写真で用いられるものを挙げることができる。
The carrier of the invention thus obtained is mixed with a toner and used for developing an electrostatic latent image. Examples of the toner include fine particles in which a colorant is dispersed in a binder resin, which are commonly used in electrophotography.

発明のダ11−!47: 本発明のキャリヤを通常使用される電子写真用トナーと
混合し7た場、合、該キャリヤはトナーを正に帯電する
ことができ、しかも適当な帯電量と著しく速い帯電速度
とを与えることができる。さらに、被覆処理によるコア
材料の電気抵抗変化が小・さく、低抵抗被覆キャリヤを
得ることが可能となり、ソリッド再現性の優れた現像剤
を提供することができる。また、被覆に基きトナーによ
る汚染が抑制されるのでキャリヤの寿命が長く、その−
果寿命の長い現像剤を得ることができ、さらに本発明の
キャリヤは溶液中への浸漬または溶液の噴霧塗布等或い
は必要に応じて加熱処理するといった簡単な工程で製造
できるなど数々の利点を有している。
Invention Da 11-! 47: When the carrier of the present invention is mixed with a commonly used electrophotographic toner, the carrier is capable of positively charging the toner, yet provides an appropriate amount of charge and a significantly faster charging rate. be able to. Furthermore, the change in electrical resistance of the core material due to coating treatment is small, making it possible to obtain a low-resistance coated carrier and providing a developer with excellent solid reproducibility. In addition, since the coating suppresses toner contamination, the carrier has a long lifespan.
In addition, the carrier of the present invention has many advantages, such as being able to obtain a developer with a long shelf life, and being able to be manufactured by a simple process such as immersion in a solution, spray application of a solution, or, if necessary, heat treatment. are doing.

実施例 以下実施例により本発明をさらに具体的に説明する。例
中の「部」は全て重量部を表わす。しかし、本発明はこ
れら実施例によって何等制限されるものではない。
EXAMPLES The present invention will be explained in more detail with reference to Examples. All "parts" in the examples represent parts by weight. However, the present invention is not limited to these Examples in any way.

実施例−7 r−パー70ロプチルグロビルトリメトキシシランのS
%アセトン溶液100部をステンレス製ビーカーに投入
し、平均粒径lθ0μmの酸化鉄粉末200部を加え、
7時間放置した。その後デカンテーションによシ大部分
の溶液を除去した後、ステンレスビーカー中の試料をビ
ーカーごと真空乾燥器に移し、アスピレータ−で減圧し
つつ常温乾燥した。次に乾燥器の温度を10Occ迄上
げ、1時間減圧乾燥した。冷却後、乾燥器から取り出し
、本発明に係るシラン化合物処理静電荷現像用キャリヤ
粒子を得た。
Example-7 S of r-par70proptylglobiltrimethoxysilane
Pour 100 parts of % acetone solution into a stainless steel beaker, add 200 parts of iron oxide powder with an average particle size lθ0 μm,
It was left for 7 hours. After removing most of the solution by decantation, the sample in the stainless steel beaker was transferred to a vacuum dryer together with the beaker, and dried at room temperature under reduced pressure with an aspirator. Next, the temperature of the dryer was raised to 10Occ, and the product was dried under reduced pressure for 1 hour. After cooling, it was taken out from the dryer to obtain carrier particles for electrostatic charge development treated with a silane compound according to the present invention.

このキャリヤ、粒子100部と、スチレン−nジチルメ
タアクリレート共再合体を結着樹脂とする電子写真用ト
ナー3部とを混合して現像剤を調製し、その帯電量を測
定したところ、トナーは正帯電(+ 7.2.5μc7
g )を示し、感光体としてアモルファスシリコン感光
体を用いた複写機で現像試験を実施したところ鮮明な画
像を与えた。
A developer was prepared by mixing 100 parts of this carrier particles and 3 parts of an electrophotographic toner containing styrene-n-dityl methacrylate copolymer as a binder resin, and the amount of charge was measured. Positive charge (+7.2.5μc7
g), and when a development test was carried out using a copying machine using an amorphous silicon photoreceptor as a photoreceptor, a clear image was obtained.

実施例−一 平均粒径コθθミク四ンの球状鉄粉をイソゾHビルアル
コールで洗浄し、さらに水で洗浄した。
Example - Spherical iron powder with an average particle diameter of θθ was washed with isozo H-byl alcohol and further washed with water.

pHをl/に調整した水酸化ナトリウム水溶液にこの洗
浄された鉄粉を30秒間浸漬し、その抜水で十分に洗浄
した。この鉄粉をさらにアセトンで洗浄した後、60q
C常圧で1時間乾燥し、冷却した。゛γ−パー70ロオ
クチルグロビルトリメトキシシラン1部をメチルエチル
ケトン70部に溶解し、前記の洗浄鉄粉100mを加え
た。−書夜放置後、デカンテーションにより薄液を除去
し、実施例−7と同様の操作で乾燥を行った。冷却後粗
大粒子をふるい分けして本発明に係るシラン化合物処理
した静電荷現像キャリヤ粒子を得た。
The washed iron powder was immersed for 30 seconds in an aqueous sodium hydroxide solution whose pH was adjusted to 1/2, and the water was drained and thoroughly washed. After further washing this iron powder with acetone, 60q
It was dried for 1 hour at normal pressure and cooled. 1 part of γ-par 70-octylglobyltrimethoxysilane was dissolved in 70 parts of methyl ethyl ketone, and 100 m of the above-mentioned washed iron powder was added. - After being left to stand overnight, the thin liquid was removed by decantation, and drying was performed in the same manner as in Example-7. After cooling, coarse particles were sieved to obtain electrostatic charge developing carrier particles treated with a silane compound according to the present invention.

実施例−/と同様に現像剤を調製したところ、帯電量6
、OμC/I  を示し、実施例−/と同様に現像試験
を実施したところ鮮明な画像を与えた。
A developer was prepared in the same manner as in Example-/, and the charge amount was 6.
, OμC/I, and when a development test was carried out in the same manner as in Example-/, a clear image was obtained.

Claims (1)

【特許請求の範囲】[Claims] コア粒子と、少なくとも末端がノ母−7two化された
有機シラン化合物の被覆層とを含む静電荷像現像用キャ
リヤ粒子。
1. A carrier particle for developing an electrostatic image, comprising a core particle and a coating layer of an organic silane compound having at least two terminal groups.
JP58098809A 1983-06-03 1983-06-03 Carrier particle for developing electrostatic charge image Pending JPS59223459A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58098809A JPS59223459A (en) 1983-06-03 1983-06-03 Carrier particle for developing electrostatic charge image

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58098809A JPS59223459A (en) 1983-06-03 1983-06-03 Carrier particle for developing electrostatic charge image

Publications (1)

Publication Number Publication Date
JPS59223459A true JPS59223459A (en) 1984-12-15

Family

ID=14229658

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58098809A Pending JPS59223459A (en) 1983-06-03 1983-06-03 Carrier particle for developing electrostatic charge image

Country Status (1)

Country Link
JP (1) JPS59223459A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5021316A (en) * 1988-10-06 1991-06-04 Daikin Industries, Ltd. Coated carriers for developing electrostatic images

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5021316A (en) * 1988-10-06 1991-06-04 Daikin Industries, Ltd. Coated carriers for developing electrostatic images

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