JPH0327050A - Developer for electrostatic charge image - Google Patents

Developer for electrostatic charge image

Info

Publication number
JPH0327050A
JPH0327050A JP1162015A JP16201589A JPH0327050A JP H0327050 A JPH0327050 A JP H0327050A JP 1162015 A JP1162015 A JP 1162015A JP 16201589 A JP16201589 A JP 16201589A JP H0327050 A JPH0327050 A JP H0327050A
Authority
JP
Japan
Prior art keywords
developer
toner
resin
powder
toner particles
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
Application number
JP1162015A
Other languages
Japanese (ja)
Other versions
JP2830082B2 (en
Inventor
Takashi Shintaku
隆 新卓
Kazuhiro Hirama
和宏 平間
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei 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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP1162015A priority Critical patent/JP2830082B2/en
Publication of JPH0327050A publication Critical patent/JPH0327050A/en
Application granted granted Critical
Publication of JP2830082B2 publication Critical patent/JP2830082B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To enhance chargeability characteristics of the developer and image quality by adding a specified compound powder to the outsides of toner particles containing a specified charge controller and using 2 kinds of specified carriers in combination with the powder. CONSTITUTION:This developer to be used is prepared by adding a basic powder of magnesium.aluminum bydroxycarbonate.hydrate represented by formula II (m is an optional integer and each of p - s is an integer satisfying prescribed relationships) to the outsides of the toner particles containing at least a resin, a colorant, and the charge controller of a quaternary ammonium salt represented by formula I (R<1> is 1 - 8 C alkyl; each of R<2> and R<3> is 1 - 18 C alkyl; and R<4> is 1 - 8 C alkyl or benzyl), and in combination with this toner adding the 2 kinds of carriers comprising a ferrite powder coated with a methylsilicone resin and a ferrite powder coated with a methylphenylsilicone resin.

Description

【発明の詳細な説明】 〈従来の技術〉 電子複写機等で使用される現像剤は、その現像工程にお
いて、例えば静電荷像が形威されている感光体等の像担
持体に一旦付着せしめられ、次に転写工程において感光
体から転写紙に転写された後、定着工程においてコピー
紙面に定着される。
[Detailed Description of the Invention] <Prior Art> During the development process, the developer used in electronic copying machines and the like is once attached to an image carrier such as a photoreceptor on which an electrostatic image is formed. The image is then transferred from the photoreceptor to transfer paper in a transfer step, and then fixed on the copy paper surface in a fixing step.

その際、潜像保持面上に形威される静電荷像を現像する
ための現像剤として、キャリアーとトナーとから或る二
或分系現像剤およびキャリアーを必要としない一或分系
現像剤(磁性トナー)が知られている。
In this case, as a developer for developing the electrostatic charge image formed on the latent image holding surface, a two-part developer consisting of a carrier and a toner and a one-part developer that does not require a carrier are used. (magnetic toner) is known.

そして、従来より現像剤に帯電性を付与するものとして
ニグロシン系染料、4級アンモニウム塩等の帯電制御剤
やキャリアのコーティング剤等が知られていた。
Conventionally, charge control agents such as nigrosine dyes and quaternary ammonium salts, carrier coating agents, and the like have been known as agents that impart chargeability to developers.

く発明が解決しようとする課題〉 しかしながら、これら従来の帯電性付与剤は、帯電性付
与効果は必ずしも満足できるものではなく、適度な帯電
性を環境等によらず安定的に示し、且つその帯電の経時
変化が好ましい形態を示すトナーを得るのは難しく、低
温低湿下、高温高湿下、又は連続複写時にカプリ等、画
像汚れが発生し、或は安定したコピー濃度が得られない
点が問題となっていた。
Problems to be Solved by the Invention> However, these conventional chargeability imparting agents do not necessarily have a satisfactory chargeability imparting effect, and they do not have the ability to stably exhibit appropriate chargeability regardless of the environment. It is difficult to obtain a toner that exhibits a favorable change over time, and the problem is that image stains such as capri occur under low temperature and low humidity conditions, high temperature and high humidity conditions, or during continuous copying, or stable copy density cannot be obtained. It became.

本発明者等はかかる課題を解決すべく鋭意検討した結果
、特定の構造式で示される4級アンモニウム塩を帯電制
御剤として含有せしめたトナー粒子に塩基性マグネシウ
ム・アルミニウム・ハイドロオキシ・カーボネート・ハ
イドレート粉末を外添してなるトナーを樹脂コートされ
たフェライト粉と混合し、且つ該樹脂としてメチルシリ
コーン樹脂およびメチルフェニルシリコーン樹脂を併用
することにより、好ましい帯電特性を示し、画質および
耐久性に優れた現像剤が得られることを見出し、本発明
に到達した. 即ち、本発明の目的は、画質の経時劣化および環境によ
る劣化の少ない、帯電特性に優れた静電荷像現像用現像
剤を提供することにある。
As a result of intensive studies to solve this problem, the present inventors have found that toner particles containing a quaternary ammonium salt represented by a specific structural formula as a charge control agent contain basic magnesium aluminum hydroxy carbonate hydride. By mixing a toner formed by externally adding rate powder with resin-coated ferrite powder and using methyl silicone resin and methyl phenyl silicone resin together as the resin, the toner exhibits favorable charging characteristics and has excellent image quality and durability. The present inventors have discovered that a developer can be obtained, and have arrived at the present invention. That is, an object of the present invention is to provide a developer for developing electrostatic images with excellent charging characteristics and less deterioration of image quality over time and environment.

〈課題を解決するための手段〉 しかして、かかる本発明の目的は、少くとも樹脂、着色
剤および下記一般式(1)で表される4級アンモニウム
塩を含むトナー粒子に塩基性マグネシウム・アルξニウ
ム・ハイドロオキシ・カーボネート・ハイドレート粉末
を外添してなるトナー、メチルシリコーン樹脂で被覆さ
れたフェライト粉並びにメチルフェニルシリコーン樹脂
で被覆されたフェライト粉を含有してなる静電荷像現像
用現像剤により容易に達或される。
<Means for Solving the Problems> Therefore, an object of the present invention is to add basic magnesium alkali to toner particles containing at least a resin, a colorant, and a quaternary ammonium salt represented by the following general formula (1). A developer for developing electrostatic images containing a toner externally added with ξnium hydroxy carbonate hydrate powder, ferrite powder coated with methyl silicone resin, and ferrite powder coated with methyl phenyl silicone resin. This can be easily achieved by drugs.

・ ・ ・ [r] (式中、R’は炭素数1〜8のアルキル基を表し、R2
およびR3はそれぞれ炭素数1〜18のアルキル基を表
し、R4は炭素数1〜8のアルキル基またはベンジル基
を表す。) (作 用) 以下、本発明を詳細に説明する。
・ ・ ・ [r] (In the formula, R' represents an alkyl group having 1 to 8 carbon atoms, and R2
and R3 each represent an alkyl group having 1 to 18 carbon atoms, and R4 represents an alkyl group having 1 to 8 carbon atoms or a benzyl group. ) (Function) The present invention will be explained in detail below.

本発明に用いられる4級アンモニウム塩は前記一般式(
1)で表される通りの4級アンモニウム塩とナフトール
スルホン酸の造塩化合物であって、具体的には例えば下
記の化合物が挙げられる.・ ・ ・(11 ・ ・ ・(3) ・ ・ ・(4) ・ ・ ・(8) ・ ・ ・(9) ・ ・ ・0■ 本発明に、使用し得る樹脂威分としては、静電荷像現像
用のトナーに適した公知の種々のものが使用できる.例
えば、スチレン系樹脂、スチレンアクリル系共重合樹脂
、ポリエステル系樹脂、エボキシ系樹脂及びこれらの混
合樹脂、また、これらのアルキル側鎖にアξノ基を有す
るもの等があるが、中でもスチレン系又はポリエステル
系の樹脂が好ましい. トナー中の一般式(1)で表される化合物の含有量は、
樹脂lOO重量部に対して0.1〜10重量部、より好
ましくは1〜3重量部とするのが好適である。
The quaternary ammonium salt used in the present invention has the general formula (
Salt-forming compounds of quaternary ammonium salt and naphtholsulfonic acid as represented by 1) include, for example, the following compounds.・ ・ ・(11 ・ ・ ・(3) ・ ・ ・(4) ・ ・ ・(8) ・ ・ ・(9) ・ ・ ・0■ Resin components that can be used in the present invention include electrostatic charge image Various known toners suitable for developing toners can be used.For example, styrene resins, styrene-acrylic copolymer resins, polyester resins, epoxy resins, and mixed resins thereof; Among them, styrene-based or polyester-based resins are preferred.The content of the compound represented by the general formula (1) in the toner is as follows:
The amount is preferably 0.1 to 10 parts by weight, more preferably 1 to 3 parts by weight, based on 100 parts by weight of the resin.

本発明で用いる着色剤としては、従来から各色トナーに
用いられているものであれば特に制限されるものではな
く、例えば黒色トナー用にはカーボンブラック等を使用
する。
The coloring agent used in the present invention is not particularly limited as long as it has been conventionally used in toners of various colors, and for example, carbon black or the like is used for black toners.

着色剤の含有率は、樹脂100重量部に対して3〜20
重量部とするのが好ましい。
The content of the colorant is 3 to 20 parts by weight per 100 parts by weight of the resin.
Preferably, it is expressed in parts by weight.

更に、本発明現像剤のトナーには、一般式(1)で表さ
れる化合物とは別に、公知のものを含めて他の帯電制御
剤、即ち、例えばポリアミン樹脂および/又はニグロシ
ン系染料等を含有せしめてもよい。
Furthermore, in addition to the compound represented by the general formula (1), the toner of the developer of the present invention may contain other charge control agents, including known ones, such as polyamine resins and/or nigrosine dyes. It may also be included.

その他、本発明現像剤のトナー構成或分として、定着性
や流動性を向上させるため、低分子量オレフィン重合体
や微粉未シリカ等の添加剤を内添または外添してもよい
In addition, as part of the toner composition of the developer of the present invention, additives such as a low molecular weight olefin polymer or finely divided silica may be added internally or externally to improve fixing properties and fluidity.

トナー粒子の製造法としては、上記の各威分をニーダー
等で混練し冷却後、粉砕し分級すればよい.トナー粒子
の平均粒径は5〜20μmが好適であ?。
Toner particles can be produced by kneading the above ingredients in a kneader or the like, cooling, pulverizing, and classifying. The average particle diameter of the toner particles is preferably 5 to 20 μm. .

一方、トナー粒子に外添すべき塩基性マグネシウム・ア
ルミニウム・ハイドロオキシ・カーボネート・ハイドレ
ートは下記一般式(II)で表されるが、 Mgp Alq  (OH)r  (COz )s  
・mHz ○・・・ (II) (式中p,q.rおよびSは2p+.3q=r+2Sを
満足する整数を表す、mは任意の整数を表す。)この中
でもM g b A l t  ( O H ) + 
x C; 0 34H20またはMga,sAl■ (
○H)13CO33.5H! ○等のハイドロタルサイ
ト類と呼ばれる化合物が好便に使用される。
On the other hand, basic magnesium aluminum hydroxy carbonate hydrate to be externally added to toner particles is represented by the following general formula (II), Mgp Alq (OH) r (COz ) s
・mHz ○... (II) (In the formula, p, q.r and S represent integers that satisfy 2p+.3q=r+2S, m represents any integer.) Among these, M g b A lt ( O H ) +
x C; 0 34H20 or Mga,sAl■ (
○H) 13CO33.5H! Compounds called hydrotalcites such as ○ are conveniently used.

この塩基性マグネシウム・アルξニウム・ハイドロオキ
シ・カーボネート・ハイドレートは脂肪酸で処理すると
一部が金属塩となるが、かかる処理後のハイドレート粉
末も本発明に好適に用い得る。
When this basic magnesium aluminum ξnium hydroxy carbonate hydrate is treated with a fatty acid, part of it becomes a metal salt, and the hydrate powder after such treatment can also be suitably used in the present invention.

又、その外添景はバインダー樹脂100重量部に対して
0.01〜1重量部とするのが好ましい.本発明現像剤
は、上記の様に製造されたトナーを、表面を被覆するシ
リコーン系樹脂の種類の異なる2種類のキャリアーと混
合して使用することが特徴である。
Further, the amount of the external additive is preferably 0.01 to 1 part by weight per 100 parts by weight of the binder resin. The developer of the present invention is characterized in that the toner produced as described above is mixed with two types of carriers having different types of silicone resins for coating the surface.

即ち、シリコーン樹脂は、ケイ素原子がシロキサン結合
を介して互いに結合し、網目状に伸び広がった巨大分子
からなり、該巨大分子の表面の、シロキサン結合を介し
て他の3以下のケイ素原子としか結合していないケイ素
原子は、通常水酸基を有しているが、この水酸基の少な
くとも一部がメチル基、またはメチル基およびフェニル
基と置き換わってなる樹脂をそれぞれメチルシリコーン
樹脂およびメチルフェニルシリコーン樹脂と称する。
That is, silicone resin consists of a macromolecule in which silicon atoms are bonded to each other via siloxane bonds and spread out in a network, and the silicone resin is composed of a macromolecule in which silicon atoms are bonded to each other through siloxane bonds and are spread out in a network. Non-bonded silicon atoms usually have hydroxyl groups, and resins in which at least a portion of the hydroxyl groups are replaced with methyl groups, or methyl groups and phenyl groups are called methyl silicone resins and methylphenyl silicone resins, respectively. .

本発明現像剤に用いるキャリアーは、少なくともメチル
シリコーン樹脂で被覆されたフェライト粉とメチルフェ
ニルシリコーン樹脂で被覆されたフェライト粉の両方を
含む.キャリアーの粒径には特に制限はないが10〜2
00μmの平均粒径を有するフェライトが好ましい。こ
れらキャリアーは、トナー1重量部に対して、5〜10
0重量部使用することが好ましく、このうちメチルフェ
ニルシリコーン樹脂で被覆されたフェライトを全キャリ
アー中5〜50wt%、より好ましくは10〜30wt
%とするのが好適である.〈実施例〉 以下、実施例により本発明を更に詳細に説明するが本発
明はその要旨を超えない限り以下の実施例によりなんら
制限されるものではない。
The carrier used in the developer of the present invention contains at least both ferrite powder coated with methyl silicone resin and ferrite powder coated with methyl phenyl silicone resin. There is no particular limit to the particle size of the carrier, but it is between 10 and 2.
Ferrite having an average grain size of 0.00 μm is preferred. These carriers may be used in an amount of 5 to 10 parts per part by weight of toner.
It is preferable to use 0 part by weight of the ferrite coated with methylphenyl silicone resin, and 5 to 50 wt% of the total carrier, more preferably 10 to 30 wt% of the ferrite coated with methylphenyl silicone resin.
It is preferable to set it as %. <Examples> Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited in any way by the following Examples unless the gist thereof is exceeded.

なお、下記実施例中単にr部」とあるのはいずれも「重
量部」を意味するものとする。
In addition, in the following examples, the term "r parts" means "parts by weight."

く実施例l〉 を配合、混練、粉砕し分級して平均粒径11μmの黒色
トナー粒子を得た。この黒色トナー粒子100部に対し
てシリカ微粉末(日本アエロジル■製R−972)0.
2部とハイドロタルサイト類化合物(MgiAlz  
(OH) ・4H.O)の脂肪酸処理された微粉末0.
3部をヘンシエルミキサーにて外添処理した。
Example 1> was blended, kneaded, pulverized and classified to obtain black toner particles with an average particle size of 11 μm. 0.0 parts of fine silica powder (R-972 manufactured by Nippon Aerosil ■) per 100 parts of the black toner particles.
Part 2 and hydrotalcite compounds (MgiAlz
(OH) ・4H. O) fatty acid treated fine powder 0.
Three parts were externally added using a Henschel mixer.

得られたトナー4部と平均粒径約100μmのメチルシ
リコーン樹脂で被覆されたフェライト粉50部とメチル
フェニルシリコーン樹脂で被覆されたフェライト粉50
部とを混合、撹拌し、現像剤を作製した。
4 parts of the obtained toner, 50 parts of ferrite powder coated with methyl silicone resin having an average particle size of about 100 μm, and 50 parts of ferrite powder coated with methyl phenyl silicone resin.
A developer was prepared by mixing and stirring the following parts.

次に、この現像剤を有機光導電体を感光体とする複写機
を用いて40″C/85〜90%RHの高温/高湿条件
で100000枚の実写テストを実施した. 実写テストに使用した補給用トナーは、上記現像剤に用
いられたトナーと同一組或のトナーである。
Next, using this developer, a photocopying machine using an organic photoconductor as a photoconductor was used to conduct a photocopy test of 100,000 sheets under high temperature/high humidity conditions of 40"C/85-90% RH.Used for photocopying test. The supplied replenishing toner is from the same group as the toner used in the developer.

実写テストの結果、iooooo枚後の実写も、コピー
の白地部の汚れであるカブリの増加がなく、又コピー黒
色部の均一性及び濃度も高く、又濃度度低下のない高温
、高湿下の厳しい環境下でも耐久性に優れたトナー及び
現像剤であった;く実施例2〉 実施例1で使用したハイドロタルサイト類化合物.の脂
肪酸処理された微粉末の使用量を0.05部とした以外
は実施例lと全く同様にしたところ100000枚の実
写テスト後にもカプリの増加がなく、又、コピーの黒地
部の均一性及び濃度も高く又、濃度低下のない耐久性に
優れたトナー現像剤が得られた。
As a result of the live-copying test, it was found that there was no increase in fog, which is dirt on the white background of the copy, even after iooooo copies were made, and the black part of the copy had high uniformity and density, and it could be used under high temperature and high humidity without any decrease in density. The toner and developer had excellent durability even under harsh environments; Example 2 Hydrotalcite compound used in Example 1. Example 1 was carried out in exactly the same manner as in Example 1, except that the amount of fine powder treated with fatty acids was changed to 0.05 part. There was no increase in capri even after a test of 100,000 copies, and the black background of the copies was uniform. A toner developer with high density and excellent durability with no decrease in density was obtained.

〈実施例3〉 ハイドロタルサイト類化合物の脂肪酸処理された微粉末
の使用量1.0部とした以外は実施例lと全く同様にし
たところ、1000000枚実写後もカブリの増加がな
く、又黒地部の均一性及び濃度も高く耐久性に優れたト
ナー、現像剤が得られた. く実施例4〉 ハイドロタルサイト類化合物の脂肪酸処理されない微粉
末を0. 3部用いた以外は実施例1と全く同様にした
ところ、iooooo枚実写テスト後もカブリの増加も
なく、又濃度の均一で、濃度低下のない耐久性に優れた
トナー、現像剤が得られた。
<Example 3> The same procedure as Example 1 was carried out except that the amount of fine powder of hydrotalcite compound treated with fatty acid was 1.0 part. There was no increase in fog even after 1,000,000 sheets were photographed. A toner and developer with excellent durability and uniformity in black areas and high density were obtained. Example 4> Fine powder of a hydrotalcite compound that is not treated with fatty acids was mixed with 0. When the same procedure as in Example 1 was carried out except that 3 copies were used, a toner and developer with excellent durability with no increase in fog, uniform density, and no decrease in density even after the ioooooo sheet actual copy test was obtained. Ta.

く実施例5〉 を配合、混練、粉砕、分級し平均粒径11amのマゼン
タトナー粒子を得た。
Example 5> was blended, kneaded, pulverized and classified to obtain magenta toner particles having an average particle size of 11 am.

このマゼンタトナ一粒子100部に対してシリ力微粉末
(日本アエロジル■製R−972)0.2部とハイドロ
タルサイト類化合物(Mg&A/!z(OH)・4H.
O)の脂肪酸処理された微粉末を0.3部ヘンシェルξ
キサーにて外添処理した.得られたマゼンタトナーを実
施例1で用いたのと全く同じキャリアーと混合して現像
剤を作製した.実施例1と同様、実写テストを実施した
所30000枚実写後も、カブリのない濃度均一性の高
いトナー及び現像剤であった。
For each 100 parts of magenta toner particles, 0.2 parts of silicate powder (R-972 manufactured by Nippon Aerosil ■) and a hydrotalcite compound (Mg&A/!z(OH).4H.
O) 0.3 part Henschel ξ of fatty acid-treated fine powder
It was treated with external additives using a kisser. The obtained magenta toner was mixed with exactly the same carrier as used in Example 1 to prepare a developer. As in Example 1, a photo-photographing test was conducted, and even after 30,000 sheets were photo-photographed, the toner and developer were free from fog and had high density uniformity.

く比較例1〉 ハイドロタルサイトi化合物を使用しない以外は、実施
例1と全く同様にトナー及び現像剤を製造し、実写テス
トを実写したところ、約3000枚実写時から白地部の
汚れすなわちカブリが増加し、コピー濃度が低下する等
問題があり、実使用出来ない現像剤であった. 〈比較例2〉 ハイドロタルサイト類化合物の微粉末を使用しなかった
以外は実施例5と全く同様にしたところ、約2000枚
実写時からカブリが増加し、コピー濃度が低下し、実用
に耐えない現像剤であった。
Comparative Example 1> A toner and developer were manufactured in exactly the same manner as in Example 1, except that the hydrotalcite i compound was not used, and a live-photographing test was conducted. From the time of about 3,000 sheets, stains on the white background, that is, fogging, were observed. This developer could not be used in practice due to problems such as increased density and decreased copy density. <Comparative Example 2> Example 5 was carried out in exactly the same manner as in Example 5 except that the fine powder of the hydrotalcite compound was not used. However, fogging increased after approximately 2,000 sheets were printed, and the copy density decreased, making it unsuitable for practical use. There was no developer.

く発明の効果〉 本発明の静電荷像現像用トナーは常に適度で且つ安定し
た帯電性を示す等帯電性能が良好で、従来問題となって
いた高温高温、低温低湿下或は連続複写時のコピー汚れ
や画像濃度の低下が少ない等使用条件に係わらず良好な
画像を与え、多大な工業的利益を提供するものである。
Effects of the Invention The toner for developing electrostatic images of the present invention has good charging performance, always exhibiting appropriate and stable charging properties, and is resistant to the conventional problems of high temperature, high temperature, low temperature and low humidity, or during continuous copying. It provides a good image regardless of the conditions of use, such as less copy staining and lowering of image density, and provides great industrial benefits.

Claims (1)

【特許請求の範囲】[Claims] (1)少くとも、樹脂、着色剤および下記一般式( I
)で表される4級アンモニウム塩を含むトナー粒子に塩
基性マグネシウム・アルミニウム・ハイドロオキシ・カ
ーボネート・ハイドレート粉末を外添してなるトナー、
メチルシリコーン樹脂で被覆されたフェライト粉並びに
メチルフェニルシリコーン樹脂で被覆されたフェライト
粉を含有してなる静電荷像現像用現像剤。 ▲数式、化学式、表等があります▼・・・〔 I 〕 (式中、R^1は炭素数1〜8のアルキル基を表し、R
^2およびR_3はそれぞれ炭素数1〜18のアルキル
基を表し、R^4は炭素数1〜8のアルキル基またはベ
ンジル基を表す。)
(1) At least a resin, a colorant and the following general formula (I
) A toner formed by externally adding basic magnesium aluminum hydroxy carbonate hydrate powder to toner particles containing a quaternary ammonium salt represented by
A developer for electrostatic image development comprising ferrite powder coated with methyl silicone resin and ferrite powder coated with methyl phenyl silicone resin. ▲There are mathematical formulas, chemical formulas, tables, etc.▼...[I] (In the formula, R^1 represents an alkyl group having 1 to 8 carbon atoms, and R
^2 and R_3 each represent an alkyl group having 1 to 18 carbon atoms, and R^4 represents an alkyl group having 1 to 8 carbon atoms or a benzyl group. )
JP1162015A 1989-06-23 1989-06-23 Developer for developing electrostatic images Expired - Lifetime JP2830082B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1162015A JP2830082B2 (en) 1989-06-23 1989-06-23 Developer for developing electrostatic images

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1162015A JP2830082B2 (en) 1989-06-23 1989-06-23 Developer for developing electrostatic images

Publications (2)

Publication Number Publication Date
JPH0327050A true JPH0327050A (en) 1991-02-05
JP2830082B2 JP2830082B2 (en) 1998-12-02

Family

ID=15746430

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1162015A Expired - Lifetime JP2830082B2 (en) 1989-06-23 1989-06-23 Developer for developing electrostatic images

Country Status (1)

Country Link
JP (1) JP2830082B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5244764A (en) * 1991-05-20 1993-09-14 Mitsubishi Kasei Corporation Electrostatic image-developing toner and developer
WO1998036686A1 (en) 1997-02-24 1998-08-27 Tanita Corporation Living body impedance measuring instrument and body composition measuring instrument
EP0928997A1 (en) * 1998-01-08 1999-07-14 Powdertech Co. Ltd. Regeneration of carrier and electrophotographic developer containing regenerated carrier

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5244764A (en) * 1991-05-20 1993-09-14 Mitsubishi Kasei Corporation Electrostatic image-developing toner and developer
WO1998036686A1 (en) 1997-02-24 1998-08-27 Tanita Corporation Living body impedance measuring instrument and body composition measuring instrument
US6393317B1 (en) 1997-02-24 2002-05-21 Tanita Corporation Living body impedance measuring instrument and body composition measuring instrument
EP0928997A1 (en) * 1998-01-08 1999-07-14 Powdertech Co. Ltd. Regeneration of carrier and electrophotographic developer containing regenerated carrier

Also Published As

Publication number Publication date
JP2830082B2 (en) 1998-12-02

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