JPS59129861A - Toner for use in powder developer - Google Patents

Toner for use in powder developer

Info

Publication number
JPS59129861A
JPS59129861A JP58004107A JP410783A JPS59129861A JP S59129861 A JPS59129861 A JP S59129861A JP 58004107 A JP58004107 A JP 58004107A JP 410783 A JP410783 A JP 410783A JP S59129861 A JPS59129861 A JP S59129861A
Authority
JP
Japan
Prior art keywords
toner
ethylene
acrylic acid
acid copolymer
powder developer
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
JP58004107A
Other languages
Japanese (ja)
Inventor
Norio Saruwatari
紀男 猿渡
Kazumasa Saito
斎藤 和正
Seiji Okada
誠二 岡田
Isao Watanabe
勲 渡辺
Toshiaki Narisawa
成沢 俊明
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.)
Fujitsu Ltd
Original Assignee
Fujitsu 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 Fujitsu Ltd filed Critical Fujitsu Ltd
Priority to JP58004107A priority Critical patent/JPS59129861A/en
Publication of JPS59129861A publication Critical patent/JPS59129861A/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
    • G03G9/08704Polyalkenes
    • 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
    • G03G9/08722Polyvinylalcohols; Polyallylalcohols; Polyvinylethers; Polyvinylaldehydes; Polyvinylketones; Polyvinylketals
    • 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
    • G03G9/08742Binders for toner particles comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08753Epoxyresins

Landscapes

  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Developing Agents For Electrophotography (AREA)

Abstract

PURPOSE:To prevent a toner from sticking and adhering to the surface of a carrier and a photosensitive plate by mixing an ethylene-acrylic acid copolymer with a toner for use in a powder developer contg. an epoxy compd. having >=one epoxy group and a colorant. CONSTITUTION:An intended powder developer toner is obtained by mixing (A) 100pts.wt. epoxycompd. having >= one epoxy group in the molecule, (B) 1- 10pts.wt. ethylene-acrylic acid copolymer expressed in the formula shown here in which n, m are each a positive integer, and X is H, methyl, or ethyl, and (C) a colorant, such as carbon black, kneading the mixture, then pulverizing and classifying it. The obtained toner has superior filming resistance due to a nonadhesive ethylene-acrylic acid copolymer incorporated in it.

Description

【発明の詳細な説明】 (1)発明の技術分野 本発明は粉体現像用トナーに関し、更に詳しくはキャリ
ア及び感光板表面への粘着、付着を防止する改良された
粉体現像用トナーに関する。
DETAILED DESCRIPTION OF THE INVENTION (1) Technical Field of the Invention The present invention relates to a toner for powder development, and more particularly to an improved toner for powder development that prevents adhesion and adhesion to carriers and photosensitive plate surfaces.

(2)従来技術 電子写真方式によるプリンタ、ファクシミリおよびコピ
アにおいて粉体現象を行う場合、現像剤としてはトナー
と呼ばれる着色樹脂粉とキャリアと呼ばれる鉄粉又はガ
ラス粉などとの混合物が使用される。
(2) Prior Art When a powder phenomenon is performed in an electrophotographic printer, facsimile, or copier, a mixture of colored resin powder called toner and iron powder or glass powder called carrier is used as the developer.

トナーは一般に粘着樹脂中にカーデンブラックなどの着
色剤を分散させたものを微粉末化したものが使用される
。一方、粘着樹脂としては一般にオリゴマーと称する低
重合体高分子が用いられることが多い。オリゴマーは低
分子量であることから溶融温度が低く、熱安定性が良好
なため電子写     ″゛真用トナーの粘着樹脂とし
て広く用いられている。
The toner generally used is a fine powder obtained by dispersing a coloring agent such as carden black in an adhesive resin. On the other hand, as the adhesive resin, a low polymer polymer generally called an oligomer is often used. Oligomers have low molecular weights, low melting temperatures, and good thermal stability, so they are widely used as adhesive resins for electrophotographic toners.

しかしながら、最近のように複写速度の増大が求められ
るような状況下にあっては、トナーとキャリアとからな
る現像剤が高速攪拌されるために相互の摩擦衝突によっ
てキャリアの表面にトナーが粘着する現象(トナーフィ
ルミング)があられれ、これが進行するとキャリアの表
面がトナーの被膜によって完全に被覆されてしまう。こ
のようなキャリアは、他のトナーと混合攪拌しても摩擦
帯電を起こさず現像能力を全く失ってしまう。更にもう
ひとつの問題点としては感光板表面へのトナー付着が存
在し、これによって印字濃度の変化やカ′ブリが発生す
る。
However, under recent circumstances where an increase in copying speed is required, the developer consisting of toner and carrier is agitated at high speed, causing the toner to stick to the surface of the carrier due to mutual frictional collisions. A phenomenon (toner filming) occurs, and as this progresses, the surface of the carrier is completely covered with a film of toner. Even when such a carrier is mixed and stirred with other toners, it does not cause triboelectric charging and completely loses its developing ability. Yet another problem is that toner adheres to the surface of the photosensitive plate, which causes changes in print density and fog.

トナーフィルミングを防止する方法としてキャリア側か
らはキャリア表面を特定のトナー樹脂に対して非粘着性
樹脂でコーティングすることなどが考えられているが、
一方、感光板表面へのトナーのねばシつきを含めた対策
をトナーに施すことも強く求められている。
As a method to prevent toner filming, the carrier side is considering coating the carrier surface with a non-adhesive resin for specific toner resins.
On the other hand, there is also a strong demand for measures to be taken to prevent the toner from sticking to the surface of the photosensitive plate.

(3)発明の目的とその構成 本発明は従来のとのような欠点を改良し、キャリア及び
感光板表面への付着、粘着を防止できるトナー樹脂を提
供することをその目的とする。
(3) Object of the invention and its structure The object of the present invention is to improve the drawbacks of the conventional toner resin and to provide a toner resin which can prevent adhesion and adhesion to the surface of a carrier and a photosensitive plate.

すなわち、本発明の粉体現像用トナーは、主成分として
分子内に少なくとも1個以上のエポキシ基を含むニーキ
シ化合物と非粘着性樹脂であるエチレン−アクリルコポ
リマーとからなることを特徴とする。前記エポキシ化合
物100重−壁部に対し、エチレン−アクリル共重合体
1〜10重量部を配合してなる、トナーが特に好゛まし
い。この場合、エチレン−アクリル共重合体が一重量部
未満であると耐フィルミング性が向上しない。又、10
重縦部?超えると耐フィルミング性がそれ以上向上しな
いし、更に粘度が高くなりすぎ、製造性が悪くなる。
That is, the powder developing toner of the present invention is characterized in that it consists of a nixy compound containing at least one epoxy group in the molecule as a main component and an ethylene-acrylic copolymer which is a non-adhesive resin. Particularly preferred is a toner containing 1 to 10 parts by weight of an ethylene-acrylic copolymer per 100 parts by weight of the epoxy compound. In this case, if the ethylene-acrylic copolymer is less than 1 part by weight, the filming resistance will not improve. Also, 10
Heavy vertical part? If it exceeds this, the filming resistance will not improve any further, and the viscosity will become too high, resulting in poor productivity.

従来、エポキシ樹脂単独を結着樹脂とした場合、出来る
だけ低い熱エネルギーで融解させ定着させ得るように分
子量の比較的低いルポリマーを用いなければならないた
めトナーフィルミングが起シやすかった。そこで本発明
者らはこのような分子量の比較的低いエポキンゾレポリ
マーに融点が低温領域にあシながら軟化温度範囲におい
ても金属などに対して非粘着性を示すエチレン−アクリ
ル共重合物を混合することによシ定眉性を劣化させるこ
となしにトナーフィルミングを防止することが可能であ
ることを見い出し本発明を完成したのである。本発明で
用いられるエポキシ化合物としては芳香族系、脂肪族系
エポキシ樹脂のいずれでもよく、例えばビスフェノール
Aとエピクロルヒドリンから得られるエポキシ樹脂、ノ
g7ツク型フェノール樹脂とエピクロルヒドリンかう得
うれるノボラック型エポキシ樹脂、フタル酸とエピクロ
ルヒドリンから得られるエポキシ樹脂、トルイジンやア
ニリン等の芳香族アミンとエピクロルヒドリンから得ら
れるエポキシ樹脂があげられる。
Conventionally, when an epoxy resin alone is used as a binder resin, toner filming tends to occur because a relatively low molecular weight polymer must be used so that it can be melted and fixed with as little thermal energy as possible. Therefore, the present inventors developed an ethylene-acrylic copolymer that has a melting point in the low temperature range but is non-adhesive to metals etc. even in the softening temperature range, in addition to the relatively low molecular weight Epoquinsol polymer. They discovered that toner filming can be prevented without deteriorating the eyebrow consistency by mixing them, and the present invention was completed. The epoxy compound used in the present invention may be either an aromatic or aliphatic epoxy resin, such as an epoxy resin obtained from bisphenol A and epichlorohydrin, or a novolak epoxy resin obtained from a phenol resin and epichlorohydrin. , epoxy resins obtained from phthalic acid and epichlorohydrin, and epoxy resins obtained from aromatic amines such as toluidine or aniline and epichlorohydrin.

又、本発明で用いられるエチレン−アクリルコポリマー
は結合エチレン量が60%以上、好ましくは80%以上
でおり、結合エチレンi60%未渦では非粘着性が失な
われてきて好ましくない。
Further, the ethylene-acrylic copolymer used in the present invention has a bound ethylene content of 60% or more, preferably 80% or more, and if the bound ethylene i is 60% unvortexed, non-stick properties are lost, which is not preferable.

更にこれらコポリマーはランダムコポリマーでるシ下記
一般式で表わされる。
Furthermore, these copolymers are random copolymers and are represented by the following general formula.

H (ここでn、mは正の整数、XはU、CU3又はC2f
K5を表わす) 本発明で使用できるエポキシ樹脂の具体例はたとえばシ
ェル社の「エピコートJ 1001.1004.100
7および1009、チバガイギー社の[アラルダイトJ
6071.7071.7072.608屯7097、;
609..7  および6099、ダウ社のrDERJ
 660.661.662.664.667.668お
よび669、ならびに大日本インキ社の「エピクロンJ
1050.3050.4050および7050などがあ
る。
H (where n, m are positive integers, X is U, CU3 or C2f
A specific example of the epoxy resin that can be used in the present invention is "Epicoat J 1001.1004.100" manufactured by Shell Co., Ltd.
7 and 1009, Ciba Geigy's [Araldite J
6071.7071.7072.608 ton 7097;
609. .. 7 and 6099, Dow rDERJ
660.661.662.664.667.668 and 669, and Dainippon Ink's "Epicron J
1050.3050.4050 and 7050.

本発明のトナーは常法によりニーダなどを用いテエポキ
シ化合物、エチレン−アクリルコポリマーに着色剤を加
え混練する。得られたトナー塊を粉砕し分級することK
よシ所望のトナーが得られる。以下実施例および比較例
によシ本発明を説明する0 (4)発明の実施例とその効果 実施例 エポキシ樹脂(商品名[エビクロン4o5o4犬日本イ
ンキ化学工業製)88重量部、エチレン結合J& 80
%のエチレン−エチルアクリル共重合物5重量部、カー
?ンブラック(商品名「ブラック・母−ルズL」キヤ?
、ト社製)5重量部、染料(商品名[ニグロシンプジ、
りEXJオリエント化学製)2重量部を100℃に加熱
したニーダで1時間混練し、次いでジェットパルピライ
ザーにより粉砕し風力分級機によシ分級してトナーAを
作製した。
The toner of the present invention is prepared by adding a coloring agent to a theepoxy compound and an ethylene-acrylic copolymer and kneading them using a kneader or the like in a conventional manner. C. Crushing and classifying the obtained toner mass
The desired toner can be obtained. The present invention will be described below with reference to Examples and Comparative Examples. (4) Examples of the Invention and Effects thereof Epoxy resin (trade name [Ebicuron 4o5o4 manufactured by Inu Nippon Ink Chemical Industry Co., Ltd.] 88 parts by weight, ethylene bond J & 80
% ethylene-ethyl acrylic copolymer, 5 parts by weight, car? Black (Product name: ``Black Mother's L'')
5 parts by weight, dye (product name: Nigrosinpuji,
EXJ Orient Chemical Co., Ltd.) was kneaded for 1 hour in a kneader heated to 100° C., then crushed with a jet pulpizer and classified with an air classifier to prepare toner A.

比較例 エチレン−エチルアクリル共重合物を使用せず、実施例
のエフJ?、+シ樹脂93重量部、カーボンブラック5
重量部、染料2重量部の組成で実施例と同様の製造工程
によシトナーBを作製した。
Comparative Example No ethylene-ethyl acrylic copolymer was used. , + 93 parts by weight of resin, 5 parts by weight of carbon black
Sitner B was produced using the same manufacturing process as in the example with a composition of 2 parts by weight and 2 parts by weight of the dye.

その結果を表1に示す。エチレン−アクリル樹脂を5重
量部添加したトナーAはトナーBに比べてキャリア表面
へのトナーフィルミング量も少なく、ドラムフィルミン
グは50,000枚とトナーBの5000枚と比べて1
0倍向上した。
The results are shown in Table 1. Toner A with 5 parts by weight of ethylene-acrylic resin added has less toner filming on the carrier surface than Toner B, with drum filming of 50,000 sheets compared to 5,000 sheets of Toner B.
Improved by 0 times.

表1 こ′i1.らトナーA、)ナーBについてキャリアどし
てTSV 1.00/200(日本鉄粉製)と組合せた
現像剤(トナー濃度3wt%)を調整し、F6715D
レーザプリンタ(富士通(株))を用いて表2に示す試
験条件でフィルミング試験を行った。
Table 1 ko'i1. For Toner A and ) Toner B, adjust the developer (toner concentration 3wt%) combined with TSV 1.00/200 (manufactured by Nippon Steel Powder) using carrier, and use F6715D.
A filming test was conducted using a laser printer (Fujitsu Ltd.) under the test conditions shown in Table 2.

表2 現 像       マグネットブラシによる反転現像
印刷速度    2000行/分 フォトリセプタ−Se  ドラム 初期電圧    +550v 定着方法     フラッシュ定着 温度条件    20〜23℃ 湿度条件    35〜74チR,I(。
Table 2 Development Reversal development with magnetic brush Printing speed 2000 lines/min Photoreceptor-Se drum Initial voltage +550v Fixing method Flash fixing temperature conditions 20-23°C Humidity conditions 35-74° R, I (.

未測定方法はまず現像剤から界面活性剤を用いてキャリ
ア表面に静電付着しているトナー粒子を除去した後、乾
燥して秤量し、メチルエチルケトンを用いてトナーの色
が出なくなるまで洗浄した後、乾燥して再び秤量する。
The unmeasured method is to first remove toner particles electrostatically adhered to the carrier surface from the developer using a surfactant, then dry and weigh, and wash with methyl ethyl ketone until the toner color disappears. , dry and weigh again.

このメチルエチルケトン洗浄による重量減少をトナーフ
ィルミング量として求めた。
The weight loss due to this methyl ethyl ketone cleaning was determined as the amount of toner filming.

米米連続縦ケイ線印字でドラム上にフィルミングが発生
し、用紙にドラム上のフィルミング像がオフセットされ
るまで印刷枚数で評価した。
Filming occurred on the drum during continuous vertical line printing, and the evaluation was based on the number of sheets printed until the filming image on the drum was offset to the paper.

特許出願人 富士通株式会社 特許出願代理人 弁理士 青 木   朗 弁理士西舘和之 弁理士 内 1)幸 男 弁理士 山 口 昭 之patent applicant Fujitsu Limited patent application agent Patent attorney Akira Aoki Patent attorney Kazuyuki Nishidate Patent attorney 1) Yukio Patent attorney Akira Yamaguchi

Claims (1)

【特許請求の範囲】[Claims] 1.1分子中に少なくとも1個以上のエポキシ基を有す
るエポキシ化合物、エチレン−アクリル共重合体および
着色剤を含んでなる、粉体現像剤用トナー。 2、前記エポキシ化合物100重量部に対し、エチレン
−アクリル共重合体1〜10重量部を配合してなる、特
許請求の範囲第1項記載のトナー。
1. A toner for a powder developer comprising an epoxy compound having at least one epoxy group in one molecule, an ethylene-acrylic copolymer, and a colorant. 2. The toner according to claim 1, wherein 1 to 10 parts by weight of an ethylene-acrylic copolymer is blended with 100 parts by weight of the epoxy compound.
JP58004107A 1983-01-17 1983-01-17 Toner for use in powder developer Pending JPS59129861A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58004107A JPS59129861A (en) 1983-01-17 1983-01-17 Toner for use in powder developer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58004107A JPS59129861A (en) 1983-01-17 1983-01-17 Toner for use in powder developer

Publications (1)

Publication Number Publication Date
JPS59129861A true JPS59129861A (en) 1984-07-26

Family

ID=11575565

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58004107A Pending JPS59129861A (en) 1983-01-17 1983-01-17 Toner for use in powder developer

Country Status (1)

Country Link
JP (1) JPS59129861A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0226399A2 (en) * 1985-12-06 1987-06-24 E.I. Du Pont De Nemours And Company Process for preparation of a stencil or resist image

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0226399A2 (en) * 1985-12-06 1987-06-24 E.I. Du Pont De Nemours And Company Process for preparation of a stencil or resist image

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