JPS6194060A - Color toner - Google Patents

Color toner

Info

Publication number
JPS6194060A
JPS6194060A JP59215711A JP21571184A JPS6194060A JP S6194060 A JPS6194060 A JP S6194060A JP 59215711 A JP59215711 A JP 59215711A JP 21571184 A JP21571184 A JP 21571184A JP S6194060 A JPS6194060 A JP S6194060A
Authority
JP
Japan
Prior art keywords
toner
acid
cross
styrene
copper phthalocyanine
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
JP59215711A
Other languages
Japanese (ja)
Inventor
Naomi Kawabe
川辺 尚己
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.)
Toshiba Corp
Original Assignee
Toshiba Corp
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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP59215711A priority Critical patent/JPS6194060A/en
Publication of JPS6194060A publication Critical patent/JPS6194060A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08702Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08706Polymers of alkenyl-aromatic compounds
    • G03G9/08708Copolymers of styrene
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08702Binders for toner particles comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08706Polymers of alkenyl-aromatic compounds
    • G03G9/08708Copolymers of styrene
    • G03G9/08711Copolymers of styrene with esters of acrylic or methacrylic acid
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/087Binders for toner particles
    • G03G9/08784Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
    • G03G9/08793Crosslinked polymers
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/09Colouring agents for toner particles
    • G03G9/0906Organic dyes
    • G03G9/0918Phthalocyanine dyes

Abstract

PURPOSE:To improve the triboelectrifiability and the color developability of a toner and to prevent the scattering of it by incorporating a cross-linked aromatic carboxylic acid resin and a copper phthalocyanine in a binary toner composed essentially of the colorant and a wax or the like. CONSTITUTION:The color toner is composed of the copper phthalocyanine to be used as the colorant, and paraffin, and a styrene resin contg. cross-linked acid component obtained by polymerizing and cross-linking a styrene type monomer, such as styrene or methylstyrene, acrylate type monomer, such as methyl acrylate of ethyl methacrylate, an acid component, such as acrylic acid or cinnamic acid, and a cross-linking agent, such as aromatic divinyl compd. diethyl carboxylic acid. The use of such a styrene resin permits the copper phthalocyanine to be enhanced in dispersibility, the color toner to be improved in triboelectrifiability and image quality to be enhanced.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は電子写真における二成分現像用のカラートナー
に関する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a color toner for two-component development in electrophotography.

〔発明の技術的背景とその問題点〕[Technical background of the invention and its problems]

一般に、電子写真装置は図面に示すように感光体1の周
囲に、感光体Iの回転方向に沿って帯電装置2.露光装
置3、現像装置4.転写装置5、剥離装置6、クリーニ
ング装置7.除電装置8を順次配設するとともに感光体
lと転写装置5との間の画像転写部9を通るべく形成さ
れた用紙搬送路IOの終端部に定着装置11を配置[ま
た構成となっている。
Generally, as shown in the drawings, in an electrophotographic apparatus, a charging device 2. Exposure device 3, development device 4. Transfer device 5, peeling device 6, cleaning device 7. The static eliminators 8 are sequentially arranged, and the fixing device 11 is arranged at the end of the paper transport path IO, which is formed to pass through the image transfer section 9 between the photoconductor l and the transfer device 5. .

そして、帯電装置2によって予め光半導体を用いた感光
体I上にコロナ放電等により電位を乗せる。
Then, a charging device 2 places a potential on the photoreceptor I using an optical semiconductor in advance by corona discharge or the like.

つぎに、その上に露光装置3により光学レンズを介して
原稿像を結像させるか、あるいはレーザ光による光信号
を当てることによね、照射された光陽に応じた電位降下
を生じせしめ、所謂静電潜像を形成させる。
Next, the exposure device 3 forms an image of the document through an optical lens, or by applying an optical signal from a laser beam, a potential drop corresponding to the irradiated light is caused, and a so-called static state is created. Forms an electrolatent image.

つぎに、現像装置t14により、帯電させた現像剤(ト
ナー)を接触あるいは近接させることにより静電潜像を
作る電界の強さに従った咽の現像側aが感光体!上に吸
着されて潜像を可視化させる。
Next, the developing device t14 brings the charged developer (toner) into contact with or in close proximity to create an electrostatic latent image.The developing side a of the throat is placed on the photoreceptor according to the strength of the electric field! The latent image is visualized by being attracted to the top.

さらに、転写装置5により、この現像剤aを電界の力に
よって用紙P上に感光体I上の現像剤を転写1〜、つい
で剥離装置6により用紙Pを感光体Iから剥離して定着
装置11に導びき、ここで熱、圧力、光等のエネルギー
を与えて定着させる。
Further, the transfer device 5 transfers the developer a on the photoreceptor I onto the paper P by the force of an electric field 1~, and then the peeling device 6 peels the paper P from the photoreceptor I, and the fixing device 11 Here, energy such as heat, pressure, and light is applied to fix the material.

以上、帯電、露光、現像、転写、定着のプロセスによっ
て複写画像が得られるようになっている。
As described above, a copied image can be obtained through the processes of charging, exposure, development, transfer, and fixing.

なお、現像剤像転写後の感光体Iの表面は次の複写に備
えるべく、クリーニング装置7、除電装置8によってク
リーニング、除電が行なわれる。これらのプロセスの中
でトナー、現像剤は現像、転写、定着、クリーニングに
大きく影響し、電子写真の中で重要な位置を占める。現
像方法としてはカスケード現像法、磁気ブラシ法、パウ
ダークラウド法、ファーブラシ現像法、ジャンピング現
像法等が知られている。大きく分類すると現像剤を感光
体の被供給部にまで搬送するのに磁力を用いる方法とそ
うでない方法とがあり、また磁力を用いる方法の中でも
トナー中に磁性粉な練り込んでトナー自身に磁性をもた
せる方法と鉄粉、フェライト粉等の磁性担体とトナーを
混合させる方法がある。磁性−成分方式の場合、酸化鉄
粉等の磁性粉を多掛に練り込むため鮮明なカラー画像を
得ることはできない。磁性二成分方式において現像剤は
樹脂、着色顔料等を混練、粉砕1〜5〜30μm程変に
分級]〜だトナーを100〜200μm程度の粒度をも
つ鉄粉、フェライト粉、あるいはニッケル粉等のキャリ
アから成る。トナーとキャリアは混合攪拌によって摩擦
帯電[7、それぞれ正、負逆の″准気曖をもつ。帯’!
を量は大ざっばに鱈って1)トナーとキャリアの摩擦帯
電系の差、11)トナー又はキャリアの電気抵抗によっ
て決まるものであるが、この帯ta’ mを制御するこ
とは現像剤の設計において最も重要なことの一つである
。帯電量はたとえば、1)ll!Il像濃度、 11)
かぶり、il+) )ナー飛散、 Iい転写効率等に影
響を及ぼし、帯電量が低すぎる場合、トナーとキャリア
を結びつける鏡像力(■帯電量の2乗)が弱くなるため
かぶりの増加、トナー飛散がおこり、逆に帯電量が高す
ぎる場合1画像濃度の低下、転写効率の低下を招く。ま
たかぶり1、トナー飛散等に関しては、トナーとキャリ
アの混合摩擦時の帯電量の立ち上がり方にも注意する必
要がある。帯電量は、常に一定の適性範囲内にコントロ
ールされる必要があるが、実際問題として連続コピーを
続けていくうちに徐々に変化していく。帯電量の制御は
一般にトナーを改良することによって行う。キャリアに
よって制御することもあるが、材質が比較的限定されて
いること、現像器の構造から制限を受けること、画質、
特に階調再現性の面から電気抵抗が予め決められてしま
う等のために一般的でない。黒色モノクロトナーの場合
、帯電量の制御法は比較的よく知られている。
The surface of the photoreceptor I after the developer image has been transferred is cleaned and neutralized by a cleaning device 7 and a static eliminating device 8 in preparation for the next copying. In these processes, toner and developer greatly influence development, transfer, fixing, and cleaning, and occupy an important position in electrophotography. As a developing method, a cascade developing method, a magnetic brush method, a powder cloud method, a fur brush developing method, a jumping developing method, etc. are known. Broadly speaking, there are methods that use magnetic force to transport the developer to the supplied part of the photoreceptor and methods that do not. Among the methods that use magnetic force, there are methods that use magnetic force to transport the developer to the supplied part of the photoreceptor. There are two methods: one method is to mix the toner with a magnetic carrier such as iron powder or ferrite powder. In the case of the magnetic component method, a clear color image cannot be obtained because a large amount of magnetic powder such as iron oxide powder is mixed in. In the magnetic two-component system, the developer is made by kneading resin, colored pigments, etc., pulverizing them and classifying them into particles of about 1 to 5 to 30 μm]. Consists of carriers. Toner and carrier are triboelectrically charged by mixing and stirring [7, each has a quasi-ambiguous atmosphere of positive and negative opposites. band'!
The amount of ta'm is roughly determined by 1) the difference in the triboelectric charging system between the toner and the carrier, and 11) the electrical resistance of the toner or carrier. This is one of the most important things in design. For example, the amount of charge is 1)ll! Il image density, 11)
Fogging, IL+)) toner scattering, I This affects transfer efficiency, etc., and if the charge amount is too low, the mirror image force (■square of the charge amount) that binds the toner and carrier becomes weak, resulting in increased fogging and toner scattering. On the other hand, if the amount of charge is too high, the density of one image will decrease and the transfer efficiency will decrease. Regarding fog 1, toner scattering, etc., it is also necessary to pay attention to how the amount of charge increases when the toner and carrier are mixed and rubbed. The amount of charge must always be controlled within a certain appropriate range, but as a practical matter, it gradually changes as continuous copying continues. The amount of charge is generally controlled by improving the toner. Although it may be controlled by the carrier, there are limitations due to the relatively limited materials, the structure of the developing device, and the image quality.
In particular, this is not common because the electrical resistance is predetermined from the viewpoint of gradation reproducibility. In the case of black monochrome toner, the method of controlling the amount of charge is relatively well known.

例えばある種の染料を添加することによりトナーの摩擦
帯電系列を変化させたり、又、着色剤と]−でのカーボ
ンブラックの種類、量を変えることによってトナーの電
気抵抗を調整[71帯電性を制御することも可能である
。しかし、これらのほとんどが有色であり、鮮明な色の
カラートナーを得るためには使用することは出来ない。
For example, the triboelectric charging series of the toner can be changed by adding a certain type of dye, and the electrical resistance of the toner can be adjusted by changing the type and amount of carbon black in the colorant [71]. It is also possible to control. However, most of these are colored and cannot be used to obtain color toners with vivid colors.

また、カラートナーに使用する有色顔料、特にアゾ系有
機顔料の場合、一般に電気抵抗はカーボンブラックに比
べて高く、従ってトナー抵抗、現像剤抵抗は高くなって
しまう。そのため現像剤を攪拌するにつれて生じた摩擦
電荷が放゛電1−にくく電荷量が増加して画像濃度が低
下するという現象が起こってくる。したがってコピーを
とるにつれて、電気特性が変化し画質が変わっていき、
また、それに伴い、スペントトナー等による現像剤の劣
化、トナー飛散による光学系の汚れ等が著しくライフ性
能は一般にかなり低い。また、カラー顔料は樹脂への分
散性が悪いため、帯電の不均一さの原因となったシ遊離
した顔料がキャリア粒子や感光体表面を汚染するなどの
悪影響を与えやすい。分散性の不良は発色不良や肌色の
原因にも々る。
Furthermore, in the case of colored pigments used in color toners, particularly azo organic pigments, electrical resistance is generally higher than that of carbon black, and therefore toner resistance and developer resistance become higher. Therefore, a phenomenon occurs in which the frictional charges generated as the developer is stirred are difficult to dissipate and the amount of charges increases, resulting in a decrease in image density. Therefore, as copies are made, the electrical characteristics change and the image quality changes.
Additionally, along with this, the developer deteriorates due to spent toner and the like, and the optical system becomes dirty due to toner scattering, etc., and the life performance is generally quite low. Furthermore, since color pigments have poor dispersibility in resin, the liberated pigments, which cause non-uniform charging, tend to have adverse effects such as contaminating carrier particles and the surface of the photoreceptor. Poor dispersibility is often the cause of poor color development and skin tone.

また色調の再現性、耐熱性、耐光性等に問題があり画質
の維持が難しいという欠点がある。
Furthermore, there are problems with color tone reproducibility, heat resistance, light resistance, etc., and it is difficult to maintain image quality.

〔発明の目的〕[Purpose of the invention]

本発明は、上記事情にもとづきなされたもので、その目
的とするところは、均一な電気特性をもち、現像剤の劣
イーし、トナー飛散が少なく、また発色性が良く、褪色
の少ない1iIIi質の安定したカラートナーを提供し
ようとするものである。
The present invention has been made based on the above-mentioned circumstances, and its purpose is to provide 1iIIIi quality that has uniform electrical characteristics, poor developer quality, little toner scattering, good color development, and less fading. The aim is to provide stable color toner.

〔本発明の概要〕[Summary of the invention]

本発明は、かかる目的を達成するために、架橋タイプか
つ酸価をもつ樹脂を用いることによって着色剤(顔料)
の分散性を良好に11、以上の問題点を解決ならI7め
るものである。
In order to achieve the above object, the present invention uses a cross-linked resin with an acid value to form a colorant (pigment).
If the above problems are solved, the dispersibility is good and the above problems are solved.

本発明の特徴とするところは着色剤樹脂及びワックス等
を主成分とする二成分現像用トナーにおいて該樹脂は製
造される際、架橋剤と共に重合され、架橋した重合体を
つくると同時に芳香族カルボン酸と反応させ架橋かつ酸
価をもった樹脂になることにある。
A feature of the present invention is that in a two-component developing toner whose main components are a colorant resin and a wax, the resin is polymerized together with a crosslinking agent during production, and at the same time a crosslinked polymer is created and an aromatic carbonaceous By reacting with acid, it becomes a crosslinked resin with an acid value.

上記酸価をもち架橋した樹脂は着色顔料特にカラートナ
ー等によく使用されているアゾ系顔料、またフタロシア
ニン系顔料の樹脂、特にスチレン系樹脂への分散を容易
にさせるものである。そのため、キャリア表面が顔料に
汚染されることが少なく現像剤の劣化を防ぐことができ
る。耐湿性にも悪影響を与えないカラートナーなt是供
できるようにしたものである。
The above-mentioned crosslinked resin having an acid value facilitates the dispersion of colored pigments, particularly azo pigments commonly used in color toners, and phthalocyanine pigments into resins, particularly styrene resins. Therefore, the surface of the carrier is less likely to be contaminated with pigment, and deterioration of the developer can be prevented. This makes it possible to provide color toners that do not adversely affect moisture resistance.

〔発明の実施例〕[Embodiments of the invention]

以下1本発明の一実施例を説明する。青色顔料である銅
フタロシアニンはその構造より正の帯電−をもち銅フタ
ロシアニンを含むトナーは帯電量が低く、かぶり、トナ
ー飛散等をおこしやすい。[1,たがって、電子吸引性
の−COOHを含有することにより帯電量が土がり良好
な帯電量を保つことが可能である。
An embodiment of the present invention will be described below. Copper phthalocyanine, which is a blue pigment, has a positive charge due to its structure, and toner containing copper phthalocyanine has a low charge amount and is likely to cause fogging, toner scattering, etc. [1. Therefore, by containing electron-attracting -COOH, it is possible to maintain a good charge amount.

また、さらにその−COOHの含有量によっても帯′准
量の調整は5T節であり01〜5.0モル%程度がよシ
良好な帯電安定性を示す。
Further, depending on the content of --COOH, the amount of charge can be adjusted to the 5T node, and a range of about 01 to 5.0 mol % exhibits good charging stability.

また架橋型のメリットとI−ては顔料の分散を良好にす
ることによりキャリア表面が顔料に汚染されることが少
なくなりスペントをおこしにくくシ、よシ良好な画質な
白えることである。
Another advantage of the crosslinked type is that by improving the dispersion of the pigment, the carrier surface is less likely to be contaminated with the pigment, less likely to cause spent, and whitening with better image quality can be achieved.

上記樹脂のスチレン系モノマーとしてはスチレン、メチ
ルスチレン、エチルスチレン、ブチルスチレン、ジメチ
ルスチレン、クロロスチレン、ジクロロスチレンでアル
Examples of the styrene monomer for the above resin include styrene, methylstyrene, ethylstyrene, butylstyrene, dimethylstyrene, chlorostyrene, and dichlorostyrene.

またアクリル系モノマーとしてはアクリル酸メチル、ア
クリル酸エチル、アクリル酸ブチル、アクリル酸プロピ
ル、アクリル酸2−エチルエキシル、メタアクリル酸メ
チル、メタアクリル酸エチル、メタアクリル酸ブチルで
ある。
The acrylic monomers include methyl acrylate, ethyl acrylate, butyl acrylate, propyl acrylate, 2-ethylexyl acrylate, methyl methacrylate, ethyl methacrylate, and butyl methacrylate.

また酸成分としてはアクリル酸、ケイヒ酸、プロトン酸
、水無プロトン酔、メタクリル酸があげられる。
Further, examples of the acid component include acrylic acid, cinnamic acid, protonic acid, anhydrous protonic acid, and methacrylic acid.

また架橋剤と1−では主に重合性の二重結合二個以上も
つ化合物であり、芳香族ジビニル化合物、ジエチル性カ
ルボン酸エステルなど全てのジビニル化合物および3つ
以上のビニル基をもつ化合物が単独、または混合物とし
2て選ばれ添加される。
In addition, crosslinking agents and 1- are mainly compounds with two or more polymerizable double bonds, and all divinyl compounds such as aromatic divinyl compounds and diethyl carboxylic acid esters and compounds with three or more vinyl groups are used alone. , or added as a mixture.

(K体1列 1 ) 一部架橋型スチレン〜アクリル共重合樹脂。(1 row of K bodies 1) Partially cross-linked styrene-acrylic copolymer resin.

アルマテックスX P A  1194 (商品名−三
井東圧製、酸価9)90重合部、ポリプロピレンワック
スハイマー550 P (商品名、三洋化成製)4市用
部、青色顔料、フタロシアニンプル4920G(商品名
;大日精化製)6.0重量部を予備混合ののち、加圧型
ニーダ−で30分間混゛練し、冷却、粗砕、微粉砕分級
を行なって、平均粒径12.(1μmの青色トナーを得
た。これをフェライトキャリアTFC−38(TDK 
)と混合1゜て現像剤をつくり、レオドライBD781
1 (来夏)にて試験を行なったところ10,000枚
の画用1.のあとも画像濃度の低下、がぶりはみられな
かった。また、30℃、85%RHの環境に24時曲放
置したあとも、かぶりの増加、トナー飛散等はみられな
かった。
Almatex After premixing 6.0 parts by weight (manufactured by Dainichiseika), the mixture was kneaded in a pressure kneader for 30 minutes, cooled, coarsely crushed, and then finely crushed to obtain an average particle size of 12.0 parts by weight. (A blue toner of 1 μm was obtained. This was transferred to the ferrite carrier TFC-38 (TDK
) and mix it 1° to make a developer, then use RheoDry BD781.
1 (next summer), we tested 10,000 sheets of 1. Even after this, there was no decrease in image density or blurring. Further, even after being left in an environment of 30° C. and 85% RH for 24 hours, no increase in fogging or toner scattering was observed.

(比較例1) スチレン−ブタジェン共重合樹脂ニポール2007J 
(商品名;日本ゼオン製、酸膜分合まず)90重量部、
ポリプロピレンワックスハイマー550P(商品名;三
洋化成製)4軍帽部、青色顔料フタロシアニンブルー4
920G(商品名;大日精化製)を実施例1と同様に1
7、青色トナーをつくり、B D 7811 (商品名
;来夏)にて試験を行ったところ、5,000枚の紙通
しによって帯iJi量が低下1〜、かぶりトナー飛散が
みられた。
(Comparative Example 1) Styrene-butadiene copolymer resin Nipole 2007J
(Product name: manufactured by Nippon Zeon, acid film does not mix) 90 parts by weight,
Polypropylene Waxheimer 550P (product name; manufactured by Sanyo Kasei) 4 military cap, blue pigment phthalocyanine blue 4
920G (trade name; manufactured by Dainichiseika) in the same manner as in Example 1.
7. When a blue toner was prepared and tested using BD 7811 (trade name: next summer), the band iJi amount decreased from 1 to 1 after passing 5,000 sheets of paper, and fogging toner scattering was observed.

〔発明の効果〕〔Effect of the invention〕

以上説明1〜たよりに、本発明によれば分散性が良くま
た帯電性の安定17たカラートナーを得ることができ画
像濃度の低下やかぶりの増加。
Based on the above explanations 1 to 1, according to the present invention, a color toner with good dispersibility and stable chargeability can be obtained, and image density decreases and fog increases.

トナー飛散等の無い安定1−だ画質を提供することがで
きる。
It is possible to provide stable image quality with no toner scattering or the like.

【図面の簡単な説明】[Brief explanation of drawings]

図面は電子写真装置の基本構成説明図である。 a・・・現像剤。 The drawing is an explanatory diagram of the basic configuration of an electrophotographic apparatus. a...Developer.

Claims (2)

【特許請求の範囲】[Claims] (1)スチレン系モノマーとアクリル酸、ケイヒ酸、プ
ロトン酸、無水プロトン酸、メタクリル酸より選択され
るモノマー及び、アクリル系モノマーと分子量調整剤、
架橋剤とを共重合成分として含む樹脂と、着色剤として
銅フタロシアニンを用いることを特徴とするカラートナ
ー。
(1) a styrene monomer and a monomer selected from acrylic acid, cinnamic acid, protonic acid, protonic acid anhydride, and methacrylic acid; an acrylic monomer and a molecular weight regulator;
A color toner characterized by using a resin containing a crosslinking agent as a copolymerization component and copper phthalocyanine as a coloring agent.
(2)スチレン系モノマー60〜90mol%、アクリ
ル酸、ケイヒ酸、プロトン酸、無水プロトン酸、メタク
リル酸より選択されるモノマー0.1〜5mol%、ア
クリル系モノマー10〜40mol%としたことを特徴
とする特許請求の範囲第1項記載のカラートナー。
(2) Styrene monomer 60-90 mol%, monomer selected from acrylic acid, cinnamic acid, protonic acid, protonic acid anhydride, methacrylic acid 0.1-5 mol%, and acrylic monomer 10-40 mol%. A color toner according to claim 1.
JP59215711A 1984-10-15 1984-10-15 Color toner Pending JPS6194060A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59215711A JPS6194060A (en) 1984-10-15 1984-10-15 Color toner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59215711A JPS6194060A (en) 1984-10-15 1984-10-15 Color toner

Publications (1)

Publication Number Publication Date
JPS6194060A true JPS6194060A (en) 1986-05-12

Family

ID=16676896

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59215711A Pending JPS6194060A (en) 1984-10-15 1984-10-15 Color toner

Country Status (1)

Country Link
JP (1) JPS6194060A (en)

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