JPS60260062A - Electrophotographic toner for heat roller fixing - Google Patents

Electrophotographic toner for heat roller fixing

Info

Publication number
JPS60260062A
JPS60260062A JP59115485A JP11548584A JPS60260062A JP S60260062 A JPS60260062 A JP S60260062A JP 59115485 A JP59115485 A JP 59115485A JP 11548584 A JP11548584 A JP 11548584A JP S60260062 A JPS60260062 A JP S60260062A
Authority
JP
Japan
Prior art keywords
vinyl
polyester resin
vinyl resin
resin
toner
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
JP59115485A
Other languages
Japanese (ja)
Other versions
JPH065392B2 (en
Inventor
Satoru Inoue
哲 井上
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.)
Ricoh Co Ltd
Original Assignee
Ricoh 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 Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP59115485A priority Critical patent/JPH065392B2/en
Publication of JPS60260062A publication Critical patent/JPS60260062A/en
Publication of JPH065392B2 publication Critical patent/JPH065392B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • G03G9/0825Developers with toner particles characterised by their structure; characterised by non-homogenuous distribution of components
    • 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
    • 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
    • G03G9/08742Binders for toner particles comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • G03G9/08755Polyesters

Abstract

PURPOSE:To improve offset resistance by consisting essentially toner particles of a vinyl resin and polyester resin in which the vinyl resin forms a continuous phase and the polyester resin forms a discontinuous phase of a specific diameter or above. CONSTITUTION:The toner particles consist essentially of the vinyl resin and polyester resin in which the vinyl resin forms the continuous phase and the polyester resin forms the discontinuous phase of >=0.5mu diameter. The vinyl resin to be used is the vinyl resin constituted of styrene alpha-methylene aliphat. monocarboxylate and the weight average mol.wt. thereof is preferably about 20,000- 400,000. The polyester resin to be used refers to the satd. or unsatd. polyester which is synthesized from a diol component and dicarboxylic acid component and has 50-150 deg.C softening point. The lower limit of the fixing temp. is thus made low and the upper limit high and therefore the region of the adequate fixing temp. is expanded and the offset resistance is improved.

Description

【発明の詳細な説明】 技術分野 この発明は、加熱ローラー定肴用電子写真トナーに関す
る。
DETAILED DESCRIPTION OF THE INVENTION TECHNICAL FIELD This invention relates to an electrophotographic toner for heated roller servings.

救迷i1 従来、ローラー表面をフッ素系樹脂など、トナーに対し
て離形性の優れた材料で形成したようなローラーを使用
する加熱ローラー定着方式においては、ローラー温度が
高過ぎると、溶融したトナー像が熱ローラーに移転し被
定着シート上に再移転するホットオフセット現象や、ロ
ーラー温度が低い場合には非溶融トナー像が再移転する
コールドオフセット現象などが発生するような問題を有
していた。
Help i1 Conventionally, in heated roller fixing systems that use rollers whose surfaces are made of a material with excellent toner release properties, such as fluororesin, if the roller temperature is too high, the molten toner may Problems include a hot offset phenomenon in which the image is transferred to the heated roller and then transferred again onto the fixing sheet, and a cold offset phenomenon in which the non-melted toner image is transferred again when the roller temperature is low. .

これらの問題を解決するには、加熱ローラー定着方式で
はコールドオフセットが起る温度からホットオフセット
温度までの温度領域を如何に広くするかというのが大き
な課題であり、そのために種々の改良が試みられていた
In order to solve these problems, a major challenge in the heated roller fixing method is how to widen the temperature range from the temperature at which cold offset occurs to the hot offset temperature, and various improvements have been attempted to this end. was.

ホットオフセット防止には、 1)結着樹脂の分子量分布を拡大する。To prevent hot offset, 1) Expanding the molecular weight distribution of the binder resin.

2)結着樹脂を部分的に架橋させ、トナーの凝集力を上
げる。
2) Partially crosslinking the binder resin to increase the cohesive force of the toner.

3)結着樹脂中に低分子量ポリオレフィンなどの離形性
のよい材料を含有させる。
3) A material with good mold releasability, such as a low molecular weight polyolefin, is included in the binder resin.

等の各方法が提案されている。しかし、上記1)、2)
の方法はホットオフセットに対しては効果があるが、定
着下限温度が上昇してしまうので、適正定着温度領域は
拡張されない。また、上記3)の方法は、ジャム巻き付
きに対しては有効であるが、耐オフセット性は十分では
ない。
Various methods have been proposed. However, above 1), 2)
Although the above method is effective against hot offset, the lower limit fixing temperature increases, so the appropriate fixing temperature range is not expanded. Furthermore, although method 3) is effective against jamming, the offset resistance is not sufficient.

コールドオフセット防止には、ポリエステルやエポキシ
樹脂など、紙に対して接着性のよい樹脂を使用すること
が提案されているが、この方法によっても耐ホツトオフ
セット性が十分でなく、適正な温度領域が拡張できない
To prevent cold offset, it has been proposed to use resins with good adhesion to paper, such as polyester or epoxy resin, but even with this method, the hot offset resistance is insufficient and it is difficult to maintain the appropriate temperature range. Cannot be expanded.

目 的 この発明は、従来技術の上記問題点を解決するものであ
る。
Purpose This invention solves the above-mentioned problems of the prior art.

構 成 この発明は、トナー粒子が、ビニル系樹脂とポリエステ
ル樹脂とを主成分として含有し、前記ビニル系樹脂が連
続相を形成し、ポリエステル樹脂が直径0.5μ以上の
不連続相を形成していることを特徴とする熱ローラー定
着用電子写真トナーである。
Structure This invention provides toner particles containing a vinyl resin and a polyester resin as main components, the vinyl resin forming a continuous phase, and the polyester resin forming a discontinuous phase having a diameter of 0.5 μ or more. This is an electrophotographic toner for thermal roller fixing.

上記構成によってこの発明のトナーは、定着下限温度が
低く、ホットオフセット濃度が高くなる。
With the above configuration, the toner of the present invention has a low minimum fixing temperature and a high hot offset density.

この発明で用いるビニル系樹脂としては、スチレン、0
−メチルスチレン、m−メチルスチレン、p−メチルス
チレン、α−メチルスチレン、p−エチルスチレン、2
,4−ジメチルスチレン、p−n−ブチルスチレン、p
−tert−ブチルスチレン、p−n−へキシルスチレ
ン、p−n−オクチルスチレン、p−n−ノニルスチレ
ン、p−n−デシルスチレン、1−n−ドデシルスチレ
ン、p−メトキシスチレン、p−フェニルスチレン、p
−クロルスチレン、3.4−ジクロルスチレンなどのス
チレン類、ビニルナフタリン類、エチレン、プロピレン
、ブチレン、イソブチレンなどのエチレン不飽和モノオ
レフィン類、塩化ビニル、臭化ビニル、弗化ビニル、酢
酸ビニル、プロピオン酸ビニル、ベンジェ酸ビニル、酪
酸ビニルなどのビニルエステル類、アクリル酸メチル、
アクリル酸エチル、アクリル酸ローブチル、アクリル酸
イソブチル、アクリル酸プロピル、アクリル1lJn−
オクチル、アクリル酸ドデシル、アクリル酸ラウリル、
アクリルM2−■デルヘキシル、アクリル酸ステアリル
、アクリル酸2−クロルエチル、アクリル酸フェニル、
α−クロルアクリル酸メチル、メタアクリル酸メチル、
メタアクリル酸エチル、メタアクリル酸プロピル、メタ
アクリル酸n−ブチル、メタアクリル酸イソブ゛チル、
メタアクリル酸n−オクチル、メタアクリル酸ドデシル
、メタアクリル酸ラウリル、メタアクリル酸2−エチル
ヘキシル、メタアクリル酸ステアリル、メタアクリル酸
フェニル、メタアクリル酸ジメチルアミノエチル、メタ
アクリル酸ジエチルアミンエチルなどのα−メチレン脂
肪族モノカルボン酸エステル類、アクリロニトリル、メ
タアクリロニトリル、アクリルアミドなどのアクリル酸
もしくはメタアクリル酸誘導体、ビニルメチルエーテル
、ビニルエチルエーテル、ビニルイソブチルエーテルな
どのビニルエーテル類1、ビニルメチルケトン、ビニル
へキシルケトン、メチルイソプロペニルケトンなどのビ
ニルケトン類、N−ビニルビロール、N−ビニルカルバ
ゾール、N−ビニルインドール、N−t’ニルビロリデ
ンなどのN−ビニル化合物などを重合させて得られるホ
モポリマー、コポリマー、ターポリマーなどがある。
The vinyl resin used in this invention includes styrene, 0
-Methylstyrene, m-methylstyrene, p-methylstyrene, α-methylstyrene, p-ethylstyrene, 2
, 4-dimethylstyrene, p-n-butylstyrene, p
-tert-butylstyrene, p-n-hexylstyrene, p-n-octylstyrene, p-n-nonylstyrene, p-n-decylstyrene, 1-n-dodecylstyrene, p-methoxystyrene, p-phenyl styrene, p
- Styrenes such as chlorostyrene and 3,4-dichlorostyrene, vinylnaphthalenes, ethylenically unsaturated monoolefins such as ethylene, propylene, butylene and isobutylene, vinyl chloride, vinyl bromide, vinyl fluoride, vinyl acetate, Vinyl esters such as vinyl propionate, vinyl benzoate, vinyl butyrate, methyl acrylate,
Ethyl acrylate, loobyl acrylate, isobutyl acrylate, propyl acrylate, acrylic 1lJn-
octyl, dodecyl acrylate, lauryl acrylate,
Acrylic M2-■Derhexyl, stearyl acrylate, 2-chloroethyl acrylate, phenyl acrylate,
α-methyl chloroacrylate, methyl methacrylate,
Ethyl methacrylate, propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate,
α- such as n-octyl methacrylate, dodecyl methacrylate, lauryl methacrylate, 2-ethylhexyl methacrylate, stearyl methacrylate, phenyl methacrylate, dimethylaminoethyl methacrylate, diethylamine ethyl methacrylate, etc. Methylene aliphatic monocarboxylic acid esters, acrylic acid or methacrylic acid derivatives such as acrylonitrile, methacrylonitrile, and acrylamide, vinyl ethers 1 such as vinyl methyl ether, vinyl ethyl ether, and vinyl isobutyl ether, vinyl methyl ketone, vinyl hexyl ketone, Homopolymers, copolymers, terpolymers, etc. obtained by polymerizing vinyl ketones such as methyl isopropenyl ketone, N-vinyl compounds such as N-vinylpyrrole, N-vinylcarbazole, N-vinylindole, and N-t'ylpyrrolidene, etc. be.

これらの多くのビニル系樹脂の中でも、スチレンα−メ
チレン脂肪族モノカルボン酸エステル類により構成され
るビニル系樹脂が好ましく、ゲルパーミェーション法に
より測定される重量平均分子量が約20,000〜40
0,000のものが好ましい。
Among these many vinyl resins, vinyl resins composed of styrene α-methylene aliphatic monocarboxylic acid esters are preferred, and have a weight average molecular weight of about 20,000 to 20,000 as measured by gel permeation method. 40
0,000 is preferred.

また、この発明で使用されるポリエステル樹脂とはジオ
ール成分とジカルボン酸成分とから合成される軟化点5
0〜150℃の飽和又は不飽和ポリエステルを指す。そ
れらの組合せ例としてはフマル酸/オキシプロピレン−
2,2−ビス(4ヒドロキシフエニル)プロパン、テレ
フタル酸/ポリエチレングリコール、無水マレイン酸/
水素添加ビスフェノールA1無水フタル酸/ポリオキシ
エチレン(2)−2,2ビス(4ヒドロキシフエニル)
プロパンなどがある。
In addition, the polyester resin used in this invention is synthesized from a diol component and a dicarboxylic acid component and has a softening point of 5.
It refers to saturated or unsaturated polyesters with a temperature of 0 to 150°C. Examples of such combinations include fumaric acid/oxypropylene-
2,2-bis(4hydroxyphenyl)propane, terephthalic acid/polyethylene glycol, maleic anhydride/
Hydrogenated bisphenol A1 phthalic anhydride/polyoxyethylene (2)-2,2bis(4hydroxyphenyl)
There are propane, etc.

トナー中の連続相をビニル系樹脂とするために、この発
明のビニル系樹脂とポリニスデル樹脂の比は50/ 5
0〜9515の範囲が好ましく、更に好ましくは75/
25〜90/10の範囲である。
In order to make the continuous phase in the toner a vinyl resin, the ratio of the vinyl resin to the polynisder resin of the present invention is 50/5.
The range is preferably 0 to 9515, more preferably 75/
It ranges from 25 to 90/10.

また不連続相を構成するポリエステル樹脂粒子の直径は
0.5μ以上、好ましくは0.5μ〜3μである。不連
続相の径は、弱い分散により達成できるが、径の測定は
、混練物をミクロトームによりカットし、薄片の透過顕
微鏡写真により行なわれる。よって、不連続層の径を見
ながら混線条件を調節すればよい。
Further, the diameter of the polyester resin particles constituting the discontinuous phase is 0.5μ or more, preferably 0.5μ to 3μ. The diameter of the discontinuous phase can be achieved by weak dispersion, but the diameter is measured by cutting the kneaded material with a microtome and taking a transmission micrograph of a thin section. Therefore, the crosstalk conditions may be adjusted while checking the diameter of the discontinuous layer.

トナー化した後のトナー断面の模式図を示すと図のよう
に、ビニル系樹脂の連続相1の中にポリエステル樹脂の
不連続相2が分散状態に存在している。
A schematic diagram of a cross section of the toner after it has been made into a toner shows that a discontinuous phase 2 of polyester resin exists in a dispersed state in a continuous phase 1 of vinyl resin.

この発明で用いられる着色剤としては種々の顔料、染料
が用いられ、特に限定されていない。例えば、カーボン
ブラック、銅フタロシアニンブルー、オイルブラック、
ニグロシン染料、群青、紺青、クロム黄、ローダミン、
カーミノ63.キナクリドン顔料、ベンジジン顔料等が
ある。
Various pigments and dyes can be used as the colorant used in this invention, and there are no particular limitations. For example, carbon black, copper phthalocyanine blue, oil black,
Nigrosine dye, ultramarine, navy blue, chrome yellow, rhodamine,
Carmino 63. Examples include quinacridone pigments and benzidine pigments.

以下実施例によって、この出願の発明を具体的に説明す
る。なお、実施網中各成分の量(部)は重量部である。
The invention of this application will be specifically explained below with reference to Examples. Note that the amounts (parts) of each component in the formulation are parts by weight.

実施例1 トナーの組成 スチレン−n・ブチルメタクリレート 共重合体く重合比8/2、分子量80,000)80部 フマル酸とエーテル化ビスフェノールAによるポリエス
テル樹脂(分子量10,000)20部 カーボンブラック 10部 上記処方の材料を2本ロールミルにて熱混練し、トナー
断面のポリエステルの不連続相の径が1μになるように
混線時間を決めた。
Example 1 Toner composition Styrene-n-butyl methacrylate copolymer (polymerization ratio 8/2, molecular weight 80,000) 80 parts Polyester resin made from fumaric acid and etherified bisphenol A (molecular weight 10,000) 20 parts Carbon black 10 The materials with the above formulation were heat-kneaded in a two-roll mill, and the mixing time was determined so that the diameter of the polyester discontinuous phase in the cross section of the toner was 1 μm.

不連続相の径は以下のように測定した。即ち混線物の小
片を2本ロール上よりとり出し冷却後ミクロトームにて
カットし約0.1μの薄片を得た。
The diameter of the discontinuous phase was measured as follows. That is, a small piece of the crosstalk was taken out from two rolls, cooled, and then cut with a microtome to obtain a thin piece of about 0.1 μm.

この薄片を透過型走査電子顕微鏡で観察し、不連続層の
径を測定した。
This thin section was observed with a transmission scanning electron microscope, and the diameter of the discontinuous layer was measured.

次に混線物は混線後2本ロールより取り出し、冷却後粉
砕し、分級して5〜20μの粒径のトナー粒子を得た。
Next, the mixed material was taken out from the two rolls after being mixed, cooled, crushed, and classified to obtain toner particles having a particle size of 5 to 20 .mu.m.

このトナー5部に対しキャリヤー鉄粉95部を混合し、
現像剤とした。
Mixing 95 parts of carrier iron powder with 5 parts of this toner,
It was used as a developer.

次にこの現像剤にて通常の電子写真法にて形成した静電
潜像を現像した後、トナー像を転写紙上に転写し以下の
通りに定着試験を行なった。
Next, an electrostatic latent image formed by a conventional electrophotographic method was developed using this developer, and then the toner image was transferred onto a transfer paper and a fixing test was conducted as follows.

定着ローラーは表面をテブロ゛ン(デュポン社)で形成
したものである(FT4γ00:■・リコー@)。この
定着器で定着を行なったところコールドオフセットは1
35℃、ホットオフセットは220℃で発生し定着温度
幅の広いことが確認できた。
The surface of the fixing roller was made of Tebron (Dupont) (FT4γ00: ■, Ricoh @). When I performed fusing with this fuser, the cold offset was 1.
It was confirmed that the fixing temperature range was wide, with hot offset occurring at 35°C and 220°C.

実施例2 トナーの組成 スチレン−2エチルへキシルアクリレート共重合体(重
合比85/15、分子量200,000)70部 テレフタル酸とエーテル化ビスフェノールAによるポリ
エステル樹脂(分子量10000)30部 カーボンブラック 10部 上記トナー組成以外は実施例1と同じ条件でトナーをつ
くり同じ条件で試験をしたところ、コールドオフセット
 130℃、ホットオフセットは230℃で、定着温度
領域が広いことがわかった。
Example 2 Toner composition Styrene-2-ethylhexyl acrylate copolymer (polymerization ratio 85/15, molecular weight 200,000) 70 parts Polyester resin made of terephthalic acid and etherified bisphenol A (molecular weight 10,000) 30 parts Carbon black 10 parts A toner was prepared under the same conditions as in Example 1 except for the above toner composition, and tested under the same conditions. It was found that the fixing temperature range was wide, with a cold offset of 130°C and a hot offset of 230°C.

実施例3 トナーの組成 スチレン−ブチルアクリレート共重合体(重合比70/
 30、分子量300,000) 85部フマル酸とエ
ーテル化ビスフェノールAによるポリエステル樹脂(分
子115,000) 15部ニグロシン染料 2部 カーボンブラック 10部 上記トナー組成以外は実施例1と同じ条件でトナーをつ
くり、同じ条件で試験をしたところ、コールドオフセッ
トは135℃、ホットオフセットは240℃であった。
Example 3 Toner composition Styrene-butyl acrylate copolymer (polymerization ratio 70/
A toner was prepared under the same conditions as Example 1 except for the above toner composition. When tested under the same conditions, the cold offset was 135°C and the hot offset was 240°C.

比較例1 実施例1と同じ組成であるが、分散を十分に行ないポリ
エステル不連続相を0.1μ以下の粒子の分散相にした
。得られたトナーに実施例1と同様な試験をしたところ
、コールドオフセットは135℃と変化はなかったが、
ホットオフセットは大いに低下して 110℃であった
Comparative Example 1 The composition was the same as in Example 1, but sufficient dispersion was performed to transform the polyester discontinuous phase into a dispersed phase of particles of 0.1 μm or less. When the obtained toner was subjected to the same test as in Example 1, the cold offset remained unchanged at 135°C.
The hot offset was greatly reduced to 110°C.

効 果 以上説明したように、この発明によれば、トナーの定着
温度の下限が低く、かつ、上限が高いので適正な定着温
麿領域が拡大され、耐オフセット性が向上する。
Effects As explained above, according to the present invention, since the lower limit of the toner fixing temperature is low and the upper limit is high, the appropriate fixing temperature range is expanded and offset resistance is improved.

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

図面は、この発明のトナーの断面を示ず模式図である。 1・・・ビニル系樹脂の連続相 2・・・ポリエステル樹脂の不連続相 特許出願人 株式会社リ コ − 代理人 弁理士 小 松 秀 岳 代理人 弁理士 旭 宏 The drawing is a schematic diagram without showing a cross section of the toner of the present invention. 1...Continuous phase of vinyl resin 2...Discontinuous phase of polyester resin Patent applicant Rico Co., Ltd. Agent Patent Attorney Hidetake Komatsu Agent Patent Attorney Hiroshi Asahi

Claims (1)

【特許請求の範囲】[Claims] トナー粒子がビニル系樹脂とポリエステル樹脂とを主成
分として含有し、前記ビニル系樹脂が連続相を形成し、
ポリエステル樹脂が直径0.5μ以上の不連続相を形成
していることを特徴とする熱ローラー定着用電子写真ト
ナー。
The toner particles contain a vinyl resin and a polyester resin as main components, the vinyl resin forming a continuous phase,
An electrophotographic toner for thermal roller fixing, characterized in that a polyester resin forms a discontinuous phase with a diameter of 0.5 μm or more.
JP59115485A 1984-06-07 1984-06-07 Electrophotographic toner for heat roller fixing Expired - Fee Related JPH065392B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59115485A JPH065392B2 (en) 1984-06-07 1984-06-07 Electrophotographic toner for heat roller fixing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59115485A JPH065392B2 (en) 1984-06-07 1984-06-07 Electrophotographic toner for heat roller fixing

Publications (2)

Publication Number Publication Date
JPS60260062A true JPS60260062A (en) 1985-12-23
JPH065392B2 JPH065392B2 (en) 1994-01-19

Family

ID=14663683

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59115485A Expired - Fee Related JPH065392B2 (en) 1984-06-07 1984-06-07 Electrophotographic toner for heat roller fixing

Country Status (1)

Country Link
JP (1) JPH065392B2 (en)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4878931A (en) * 1971-12-30 1973-10-23
JPS54114245A (en) * 1978-02-27 1979-09-06 Fuji Xerox Co Ltd Electrophotographic toner composition
JPS57136659A (en) * 1981-02-18 1982-08-23 Hitachi Metals Ltd Toner grain for electrostatic charge latent image development
JPS58159546A (en) * 1982-03-17 1983-09-21 Sekisui Chem Co Ltd Toner resin for developing electrostatic image
JPS58187946A (en) * 1982-04-28 1983-11-02 Hitachi Metals Ltd Electrophotographic developer
JPS58190957A (en) * 1982-04-30 1983-11-08 Hitachi Metals Ltd Electrophotographic developer
JPS58196549A (en) * 1982-05-12 1983-11-16 Hitachi Metals Ltd Developer for electrophotography
JPS58198049A (en) * 1982-05-14 1983-11-17 Dainippon Ink & Chem Inc Electrostatic image developing toner
JPS60244956A (en) * 1984-05-21 1985-12-04 Ricoh Co Ltd Electrophotographic toner composition

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4878931A (en) * 1971-12-30 1973-10-23
JPS54114245A (en) * 1978-02-27 1979-09-06 Fuji Xerox Co Ltd Electrophotographic toner composition
JPS57136659A (en) * 1981-02-18 1982-08-23 Hitachi Metals Ltd Toner grain for electrostatic charge latent image development
JPS58159546A (en) * 1982-03-17 1983-09-21 Sekisui Chem Co Ltd Toner resin for developing electrostatic image
JPS58187946A (en) * 1982-04-28 1983-11-02 Hitachi Metals Ltd Electrophotographic developer
JPS58190957A (en) * 1982-04-30 1983-11-08 Hitachi Metals Ltd Electrophotographic developer
JPS58196549A (en) * 1982-05-12 1983-11-16 Hitachi Metals Ltd Developer for electrophotography
JPS58198049A (en) * 1982-05-14 1983-11-17 Dainippon Ink & Chem Inc Electrostatic image developing toner
JPS60244956A (en) * 1984-05-21 1985-12-04 Ricoh Co Ltd Electrophotographic toner composition

Also Published As

Publication number Publication date
JPH065392B2 (en) 1994-01-19

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