JPS6249362A - Resin for electrophotographic toner - Google Patents

Resin for electrophotographic toner

Info

Publication number
JPS6249362A
JPS6249362A JP60189213A JP18921385A JPS6249362A JP S6249362 A JPS6249362 A JP S6249362A JP 60189213 A JP60189213 A JP 60189213A JP 18921385 A JP18921385 A JP 18921385A JP S6249362 A JPS6249362 A JP S6249362A
Authority
JP
Japan
Prior art keywords
resin
toner
weight
aromatic vinyl
copolymer
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
JP60189213A
Other languages
Japanese (ja)
Inventor
Akimasa Nomura
野村 顕正
Nobuyasu Oota
信保 太田
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.)
Zeon Corp
Original Assignee
Nippon Zeon 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 Nippon Zeon Co Ltd filed Critical Nippon Zeon Co Ltd
Priority to JP60189213A priority Critical patent/JPS6249362A/en
Publication of JPS6249362A publication Critical patent/JPS6249362A/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
    • G03G9/08737Polymers derived from conjugated dienes
    • 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

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)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the title toner having an improved image concentration and an anti-extracting property against a chemicals by incorporating a specific copolymer composed of an aromatic vinyl and a conjugated diene and a specific copolymer composed of the aromatic vinyl and an saturated acid ester to the title resin. CONSTITUTION:The title toner comprises 55-95wt% the copolymer (the resin A) having 2,000-50,000 a number average molecular weight composed of 98-80wt% the aromatic vinyl and 2-20wt% the conjugated diene, and 45-5wt% the copolymer (the resin B) having 100,000-1000,000 the number average molecular weight composed of 100-50wt% the aromatic vinyl and 0-50wt% the unsatd. acid ester. The compounding ratio of the resin A and B is 55-95wt%, preferably 65-90wt% the former and 45-5wt%, preferably 35-10wt% the latter. Thus, the title resin which has a stable quality, and is easy to grind into pieces and has the high image concentration and the excellent anti-extracting property against the chemicals is obtd.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、電子写真法において得られる静1!潜像を現
像するだめのトナー、特に熱定着型現像用トナー用樹脂
に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention is directed to the electrophotography of electrophotography. The present invention relates to a toner for developing a latent image, particularly a resin for a heat-fixing type developing toner.

(従来の技術) 一般にこの種のトナーによシ現像されて得られるトナー
像は転写紙等に定着される必要があり、その定着法とし
ては加熱定着法が広く使用されている0このうち、特に
加熱ローラ定着器による定着法は・接触塵の定着法であ
るため熱効率が高く、比較的低温の熱源によシ確実にト
ナー像を定着せしめることができ、更に転写紙がジャム
を起こした場合にも発火の危険が極めて少ない点で好ま
しい。
(Prior Art) Generally, the toner image obtained by developing with this type of toner needs to be fixed on a transfer paper or the like, and the heat fixing method is widely used as the fixing method. In particular, the fixing method using a heating roller fixing device has high thermal efficiency because it is a contact dust fixing method, and can reliably fix the toner image using a relatively low-temperature heat source. It is preferable because there is very little risk of ignition.

しかして加熱ローラ定着器の如(加熱体を接触せしめる
ことによシトナー画像を定着せしめる場合には、加熱体
にトナーの一部が付着して後続の画像部分に転写される
いわゆるオフセット現象が生ずる恐れがある。このオフ
セット現象は、加熱によって溶融したトナーの粘弾性が
適当でなくて過大又は過小のときに生ずるものであり、
従ってオフセット現象が生じない温度範囲はトナーの主
成分のひとつである樹脂の種類及びトナー成分の種類、
含有量等によって左右される。特にオフセット温度を上
げるには樹脂の分子iを上げるのが有効である。
However, when a toner image is fixed by bringing a heating element into contact with a heated roller fixing device, a so-called offset phenomenon occurs in which a portion of the toner adheres to the heating element and is transferred to the subsequent image area. This offset phenomenon occurs when the viscoelasticity of the toner melted by heating is inappropriate and is either too large or too small.
Therefore, the temperature range in which the offset phenomenon does not occur depends on the type of resin, which is one of the main components of toner, and the type of toner components.
It depends on the content etc. In particular, it is effective to increase the resin molecule i in order to increase the offset temperature.

一方定着温度は、省エネルギーの観点からより低(する
ことが要請されておシ、それに対応するには樹脂を低分
子量にする方が有効である。ところが低分子量にすると
先に述べたオフセット現象が生じてしまう。
On the other hand, the fixing temperature is required to be lower from the viewpoint of energy saving, and it is more effective to lower the molecular weight of the resin to meet this requirement. However, when the molecular weight is lower, the offset phenomenon mentioned earlier occurs. It will happen.

したがって、定着可能温度幅(定着可能な最低温度とオ
フセット現象が生じはじめる温度との幅)が広いほど好
ましく、そのためには例えば特開昭54−114245
で提案されている様に低分子量樹脂と高分子量樹脂とを
混合することが有効であるとされている。ところがこの
提案で具体的に開示されている官能基を有するスチレン
系低分子量樹脂とスチレン−ブタジェン系高分子量樹脂
との混合物を用いても、定着可能温度幅は必らずしも広
(ならない〇 ・また・低分子ll1t城と高分子量酸とを有するスチ
レン−ブタジェン共重合樹脂は、重合時ゲルが発生しや
すく品質が不安定であシ、しかも粉砕が困難であるとい
う欠点が解決されていない、・一方、定着されたトナー
の画(II濃度を上けるには、現f象時により多くのト
ナーを感光体ドラム上に付着させることが重要である。
Therefore, the wider the fixable temperature range (the range between the lowest fixable temperature and the temperature at which the offset phenomenon begins), the better.
It is said that it is effective to mix a low molecular weight resin and a high molecular weight resin as proposed in . However, even if a mixture of a styrene-based low-molecular-weight resin having a functional group and a styrene-butadiene-based high-molecular-weight resin as specifically disclosed in this proposal is used, the fixable temperature range is not necessarily wide.・In addition, the styrene-butadiene copolymer resin, which has a low-molecular-weight compound and a high-molecular-weight acid, tends to form gel during polymerization, resulting in unstable quality, and furthermore, the disadvantages of being difficult to crush have not been solved. , · On the other hand, in order to increase the density of the fixed toner image (II), it is important to deposit as much toner on the photoreceptor drum at the time of the phenomenon.

そしてこのトナー付着量を制御するには、トナー帯N量
を最適化する必要がちり、一般的には帯電制御剤が用い
られる。ところが帯電制御剤を用いてもそれと樹脂との
組合せによってはトナー付着量の制御が困難な場合が多
(、特に正帯電にしたときの画体濃度の向上が待望され
ている。
In order to control the amount of toner adhesion, it is necessary to optimize the amount of toner band N, and generally a charge control agent is used. However, even if a charge control agent is used, it is often difficult to control the amount of toner adhesion depending on the combination of the charge control agent and the resin (in particular, there is a long-awaited improvement in image density when positively charged).

又、トナーを使用したコピー用紙をデスクマントの中に
密着してはさんでお(と、紙がデスクマットからはがれ
ない場合がある。これは、一般にデスクマットが塩化ビ
ニール樹脂に可盟剤を混合して作られたものであって、
その可盟剤が紙に定着したトナーを溶かし融着すること
による現象であるが、このようなトナーの薬品抽出性は
前記特開昭54−114245で具体的に開示されてい
る樹脂混合物を用いても解決されがたいのが実情である
Also, if copy paper containing toner is tightly sandwiched inside the desk cloak, the paper may not peel off from the desk mat.This is because desk mats generally contain a binder agent in the vinyl chloride resin. It is made by mixing
This phenomenon is caused by the plasticizing agent melting and fusing the toner fixed on the paper, but the chemical extractability of the toner can be improved by using a resin mixture specifically disclosed in JP-A-54-114245. The reality is that it is difficult to solve the problem.

(発明が解決しようとする問題点) したがって本発明の目的は、定着可能温度幅が広く、品
質が安定であシ、粉砕が容易であシ、画像濃度が高く、
しかも耐薬品(特に可辺剤〕抽出性が優れた電子写真ト
ナー用樹脂を提供することにある。
(Problems to be Solved by the Invention) Therefore, the objects of the present invention are to provide a wide fixable temperature range, stable quality, easy pulverization, high image density, and
Moreover, it is an object of the present invention to provide a resin for electrophotographic toners which has excellent chemical resistance (particularly ablasts) extraction properties.

(問題点を解決するための手段) 本発明のこの目的は、数平均分子量が2.000〜s 
o、o o oである芳香族ビニル98〜80重量%及
び共役シェフ2〜20重量係の共重合体(樹脂A)55
〜95重tq6.と数平均分子量が100,000共重
合体(樹脂B)45〜5重盆チとよりなることを特徴と
する電子写真トナー用樹脂によって達成される。
(Means for Solving the Problems) This object of the present invention is to achieve a number average molecular weight of 2.000 to s.
Copolymer (resin A) of 98 to 80% by weight of aromatic vinyl o, o o o and 2 to 20% by weight of conjugated chef (resin A) 55
~95 tq6. and a number average molecular weight of 100,000 and a copolymer (resin B) of 45 to 5 times.

本発明における樹脂Aの共重合体を構成する微香族ビニ
ルはスチレン、ビニルトルエン及ヒα−〆ナルスチレン
等(好ましくはスチレン)から選択され、共役ジエンは
ブタジェン、イソグレン及び1,3−ペンタジェン等(
好ましくはブタジェン)から選択される。なおこの共重
合体は芳香族ビニル及び共役ジエンのほかにこれらと共
重合可能な単量体成分を共重合体中30重量%以下の範
囲で含有することができる。その単量体の例としてアク
リル酸、メタクリル酸等の不飽和酸;アクリヤ酸メチル
、アクリル酸エチル、アクリル酸グロビル、アクリル醗
ブチル、アクリル酸2−エチルヘキシル、メタクリル酸
メチル、メタクリル酸エチル、メタクリル酸プロピル、
メタクリル酸ブチル、メタクリル#!2−エチルへ中シ
ル、メタクリル酸ジメチルアミノエチル、メタクリル酸
ジエチルアミノエチル等の不飽和酸エステル:アクリロ
ニトリル、アクリルアミド等のその他の不飽和酸鰐導体
;エチレン、プロピレン、ブチレン等のエチレン性不飽
和モノオレフィンなどが挙げられる・この共重合組成は
、ガラス転移点が40〜80℃となる範囲で適宜決定さ
れる。ガラス転岱点が40℃未満の場合には樹脂同志が
ブロッキングしやす(、一方80℃を越えると、トナー
を粉砕することが困難となる。
The slightly aromatic vinyl constituting the copolymer of resin A in the present invention is selected from styrene, vinyltoluene, α-alpha-nalstyrene, etc. (preferably styrene), and the conjugated diene is selected from butadiene, isogrene, 1,3-pentadiene, etc.
butadiene). In addition to the aromatic vinyl and the conjugated diene, this copolymer may contain a monomer component copolymerizable with these in an amount of 30% by weight or less in the copolymer. Examples of such monomers include unsaturated acids such as acrylic acid and methacrylic acid; methyl acrylate, ethyl acrylate, globil acrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, and methacrylic acid. propyl,
Butyl methacrylate, methacrylic #! Unsaturated acid esters such as 2-ethyl tones, dimethylaminoethyl methacrylate, and diethylaminoethyl methacrylate; other unsaturated acid conductors such as acrylonitrile and acrylamide; ethylenically unsaturated monoolefins such as ethylene, propylene, butylene, etc. This copolymerization composition is appropriately determined within a range where the glass transition point is 40 to 80°C. When the glass tipping point is less than 40°C, the resins tend to block each other (on the other hand, when it exceeds 80°C, it becomes difficult to crush the toner.

また、数平均分子量(Mn )が2,000未満である
と定着時のオフセット現象が著しく、共役ジエンの共重
合割合が2C1を越えるか、Mnが50、000を越え
た場合は不安定なゲルが発生しやすく品質が不安定にな
ったり、機械的な粉砕が困酢どなる。好ましいMnはs
、ooo〜40.0口0である。共役ジエンの共重合割
合が2%未満であるとトナーを正帯電性に制御すること
がむすかしく、デスクマットにトナーが融着しやす(な
る。
In addition, if the number average molecular weight (Mn) is less than 2,000, the offset phenomenon during fixing will be significant, and if the copolymerization ratio of conjugated diene exceeds 2C1 or Mn exceeds 50,000, the gel will become unstable. This tends to cause the quality to become unstable, and mechanical grinding becomes difficult. Preferable Mn is s
, ooo~40.0 mouths 0. If the copolymerization ratio of the conjugated diene is less than 2%, it will be difficult to control the toner to be positively chargeable, and the toner will easily fuse to the desk mat.

本発明における樹脂Bの共重合体を構成する芳香族ビニ
ル及び不飽和酸エステルとしては、樹脂Aにおけると同
様のものが挙げられる。また、その他の共重合可能な単
量体成分を共重合体中20重重量以下の範囲で含有する
ことができる0その例として樹脂Aにおけると同様のも
の及びジビニルベンゼンのような多官能性単量体が挙げ
られる〇樹脂Bにおける芳香族ビニルと不飽和酸エステ
ルとの割合は共重合体のガラス転移点が40〜80℃と
なる範囲で適宜決定されるが、通常は芳香族ビニル10
0〜50重量%、不飽和酸エステル0〜50重i%であ
る。樹脂Bのガラス転移点が40〜80℃の範囲をはず
れた場合は樹脂Aに訃けると同様の問題が起こる。さら
に、樹脂BのMnが10Q、000未満の場合には、オ
フセット防止効果が得られない。一方、1. OQ 0
.000を越えた場合には、トナーを製造する際の機械
的粉砕が困難となる。
As the aromatic vinyl and unsaturated acid ester constituting the copolymer of resin B in the present invention, the same ones as in resin A can be mentioned. In addition, other copolymerizable monomer components may be contained in the copolymer in an amount of 20 weight or less. Examples include those similar to those in resin A and polyfunctional monomers such as divinylbenzene. The ratio of aromatic vinyl and unsaturated acid ester in resin B is appropriately determined within a range such that the glass transition point of the copolymer is 40 to 80°C, but usually aromatic vinyl 10
0 to 50% by weight, and 0 to 50% by weight of unsaturated acid ester. If the glass transition point of resin B is outside the range of 40 to 80°C, the same problems as resin A will occur. Furthermore, if the Mn of resin B is less than 10Q,000, no offset prevention effect can be obtained. On the other hand, 1. OQ 0
.. If it exceeds 000, mechanical pulverization during toner manufacturing becomes difficult.

樹脂Aと樹脂Bとの混合割合は前者55〜95重量慢好
ましくは65〜90重i−優、後者45〜   。
The mixing ratio of resin A and resin B is 55 to 95% by weight for the former, preferably 65 to 90% by weight for the former, and 45 to 45% for the latter.

5重量%好ましくは35〜10重量%とすることが必要
である。前者が55J量−未満であると、トナーを正帯
電性に制御することがむすがしく、かつ耐薬品抽出性が
不良となる。一方、前者が95重量−を越えると、定着
可能温度幅が10’Q以下と狭くなり実用的でない〇 樹脂Aと樹脂Bの混合はいかなる方法で行ってもよい。
It is necessary to set the amount to 5% by weight, preferably 35 to 10% by weight. If the former amount is less than 55 J, it is difficult to control the toner to be positively chargeable, and the chemical extraction resistance becomes poor. On the other hand, if the former exceeds 95% by weight, the fixable temperature range becomes narrow to 10'Q or less and is not practical. Resin A and resin B may be mixed by any method.

例えば130〜160℃の温度でロール・ニーダ−1混
練屋押出機などで溶融混練したシ、ラテックス状態で混
合して共凝固、乾燥させたり、溶液状態で混合して溶媒
をとばしてスチーム凝固させたシすることによシ得られ
る。
For example, it is melt-kneaded using a roll kneader-1 kneader extruder at a temperature of 130 to 160°C, mixed in a latex state, co-coagulated, and dried, or mixed in a solution state and then steam-solidified after evaporating the solvent. You can gain by doing something.

本発明の樹脂を用いてトナーを調製するに際しては通常
の添加剤が使用される。着色剤としては任意の顔料又は
染料が使用出来るが特にカーボンブランクが有効である
0正帯電制御剤としてはニゲ。シン、セチルピリジウム
クロライドなどが使用される。又、オフセット防止剤と
して一般的に使われているワックス又はボリプロビレン
ナトヲ併用すれば、更に定着可能温度幅を広げることが
可能となる。
Conventional additives are used in preparing toners using the resins of the present invention. Any pigment or dye can be used as the coloring agent, but carbon blank is particularly effective. Cyn, cetylpyridium chloride, etc. are used. Furthermore, if wax or polypropylene nato, which are commonly used as an offset preventive agent, are used in combination, it is possible to further widen the fixable temperature range.

なお、トナー組成物は一般に1成分トナーとして磁性粉
を内包しているものと、2成分トナーとしてキャリアー
と混合して使用するものとに区別されるが、本発明の樹
脂はいずれにも使用することが可能である。
Note that toner compositions are generally classified into those that contain magnetic powder as a one-component toner and those that are used as a two-component toner mixed with a carrier, and the resin of the present invention can be used in both. Is possible.

(実施例) 次に本発明を実施例により具体的に説明する〇チ及び部
数は重量基準である。
(Examples) Next, the present invention will be specifically explained with reference to Examples. All numbers and parts are based on weight.

実施例1 表に示す樹脂Aと樹脂Bとを所定の割合で140℃のロ
ールで予め10分間溶溶融金し、その後カーボンブラン
クが10−1帯電制御剤ニグロシンが10%となるよう
・これらを添加していきトナー組成物を得た。冷却後、
ジェットミルで微粉砕し、さらに風力分級にて平均粒径
15ミクロンのトナーを得た〇 上記トナーを鉄粉キャリヤーと混合し、デベロッパーを
作成し有機感光体上に通常の電子写真法で静電潜像を形
成した後現像し、これを普通紙にコロナ放電によシ転写
し、シリコン−テフロン熱ローラーにより熱定着し、下
記の評価を行った。
Example 1 Resin A and Resin B shown in the table were melted in a predetermined ratio with a roll at 140°C for 10 minutes, and then they were melted so that the carbon blank was 10-1 and the charge control agent nigrosine was 10%. A toner composition was obtained. After cooling,
A toner with an average particle size of 15 microns was obtained by finely pulverizing it with a jet mill and further by air classification. The above toner was mixed with an iron powder carrier to create a developer, and electrostatically applied onto an organic photoreceptor using a normal electrophotographic method. After forming a latent image, it was developed, transferred to plain paper by corona discharge, and thermally fixed using a silicone-Teflon thermal roller, and the following evaluations were performed.

結果を第1表に示す。The results are shown in Table 1.

定着性:加熱定着ローラー(画像面はテフロンゴムロー
ラー)の表面温度を所定の温度に設定し、普通紙に転写
したペタ黒画像を通す。ローラーの表面温度を10℃毎
変えてローラー上に付着したトナーが同じ紙上の白い部
分に再転写される現象(オフセット現象、)を判定しそ
の発生下限温度をTH,とした。 一方定着性の判定は
砂消しゴムがついた摩擦子で上記ペタ黒画像を5回往復
してこずつ九後の画像濃度が摩擦前のそれと比較して7
0%以上を維持している場合に定着され九と判定し、そ
の下限の温度をTfとした◇ 画像濃度:上記と同様な方法で電子写真テストチャート
を複写して画像を得る。その黒い帯状の部分に光を照射
しその反射濃度をデジタルで表示する反射濃度計で画像
濃度を測定する。
Fixing properties: Set the surface temperature of a heated fixing roller (the image surface is a Teflon rubber roller) to a predetermined temperature, and pass the peta black image transferred onto plain paper. The surface temperature of the roller was changed every 10° C. to determine the phenomenon (offset phenomenon) in which the toner adhering to the roller was retransferred to a white area on the same paper, and the lower limit temperature for this occurrence was defined as TH. On the other hand, the fixability was determined by moving the above-mentioned peta black image back and forth 5 times with a friction element equipped with a sand eraser, and comparing the image density after 9 times with that before friction.
When the temperature is maintained at 0% or more, it is determined that the image is fixed, and the lower limit temperature is defined as Tf. ◇ Image density: An image is obtained by copying an electrophotographic test chart in the same manner as above. The image density is measured using a reflection densitometer that shines light onto the black strip and digitally displays the reflected density.

デスクマットへのトナーの融着性;べた黒にコピーした
面をデスクマット側にむけて一昼夜放置後の紙のデスク
マットからのはがれ易さで判定し九〇表より、本発明に
よるトナーは定着性、画像濃度及びデスクマットへの融
着性のいずれもが良好であることがわかる。
Adhesion of the toner to the desk mat: Judging by the ease with which the paper peels off from the desk mat after leaving the solid black copy side facing the desk mat for a day and night. From Table 90, the toner according to the present invention has a good adhesion property. It can be seen that all of the properties, image density, and adhesion to the desk mat are good.

実施例2 実施例1本発明例と同じ組成の樹脂を用いて、0.3μ
の磁性粉40チ、ニグロシンt5%、樹脂58.5%の
組成となるよう各成分を140℃のロールで浴融混練し
、粒径15μの1成分トナーを実施例1と同様な方法で
作製し、その評価を行ったところ、定着性Tf 175
℃、TH0200℃、画像濃度t3、デスクマットへの
融着性○と曳好な結果が得られた。
Example 2 Using a resin with the same composition as Example 1 of the present invention, 0.3μ
A one-component toner with a particle size of 15 μm was prepared in the same manner as in Example 1 by melt-kneading each component with a roll at 140° C. to obtain a composition of 40% magnetic powder, 5% Nigrosine T, and 58.5% resin. When the evaluation was performed, the fixability Tf was 175.
℃, TH0200℃, image density t3, and good adhesion to the desk mat.

実施例3 実施例1本発明例で用いた樹脂の代シに第2表に示す樹
脂を用いたほかは実施例1と同様の実股を行った。結果
を第2表に示す。
Example 3 Example 1 The same method as in Example 1 was carried out except that the resins shown in Table 2 were used instead of the resins used in the examples of the present invention. The results are shown in Table 2.

Claims (1)

【特許請求の範囲】[Claims] 数平均分子量が2,000〜50,000である芳香族
ビニル98〜80重量%及び共役ジエン2〜20重量%
の共重合体55〜95重量%と、数平均分子量が100
,000〜1,000,000である芳香族ビニル10
0〜50重量%及び不飽和酸エステル0〜50重量%の
共重合体45〜5重量%とよりなることを特徴とする電
子写真トナー用樹脂。
98-80% by weight of aromatic vinyl having a number average molecular weight of 2,000-50,000 and 2-20% by weight of conjugated diene
copolymer of 55 to 95% by weight and a number average molecular weight of 100
,000-1,000,000 aromatic vinyl 10
A resin for electrophotographic toner, comprising 45 to 5% by weight of a copolymer of 0 to 50% by weight and 0 to 50% by weight of an unsaturated acid ester.
JP60189213A 1985-08-28 1985-08-28 Resin for electrophotographic toner Pending JPS6249362A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60189213A JPS6249362A (en) 1985-08-28 1985-08-28 Resin for electrophotographic toner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60189213A JPS6249362A (en) 1985-08-28 1985-08-28 Resin for electrophotographic toner

Publications (1)

Publication Number Publication Date
JPS6249362A true JPS6249362A (en) 1987-03-04

Family

ID=16237440

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60189213A Pending JPS6249362A (en) 1985-08-28 1985-08-28 Resin for electrophotographic toner

Country Status (1)

Country Link
JP (1) JPS6249362A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5084368A (en) * 1987-07-10 1992-01-28 Mitsui Toatsu Chemicals, Incorporated Electrophotographic toner
US5575964A (en) * 1993-08-19 1996-11-19 Sumitomo Chemical Company, Limited Method for producing silica-alumina fiber

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5084368A (en) * 1987-07-10 1992-01-28 Mitsui Toatsu Chemicals, Incorporated Electrophotographic toner
US5362595A (en) * 1987-07-10 1994-11-08 Mitsui Toatsu Chemicals, Incorporated Electrophotographic toner production process
US5575964A (en) * 1993-08-19 1996-11-19 Sumitomo Chemical Company, Limited Method for producing silica-alumina fiber

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