JPS62119548A - Electrophotographic toner - Google Patents

Electrophotographic toner

Info

Publication number
JPS62119548A
JPS62119548A JP60258475A JP25847585A JPS62119548A JP S62119548 A JPS62119548 A JP S62119548A JP 60258475 A JP60258475 A JP 60258475A JP 25847585 A JP25847585 A JP 25847585A JP S62119548 A JPS62119548 A JP S62119548A
Authority
JP
Japan
Prior art keywords
toner
charge
charge imparting
imparting agent
silica
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
JP60258475A
Other languages
Japanese (ja)
Inventor
Katsuji Ko
勝治 胡
Norio Saruwatari
紀男 猿渡
Tsuneo Watanuki
恒夫 綿貫
Yoshimichi Katagiri
善道 片桐
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 JP60258475A priority Critical patent/JPS62119548A/en
Publication of JPS62119548A publication Critical patent/JPS62119548A/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
    • G03G9/097Plasticisers; Charge controlling agents
    • G03G9/09708Inorganic compounds
    • G03G9/09725Silicon-oxides; Silicates

Abstract

PURPOSE:To reduce fogging and scattering of a toner by mixing a resin with a mixture of an electrostatic charge imparting material and a hydrophobic silica, and then, melting and kneading said material, said silica, and said binder. CONSTITUTION:The electrostatic charge imparting material can be uniformly dispersed into the binder resin powder by mixing the hydrophobic silica with said material pulverized into <=5mum diameter to prevent agglomeration of said material and improving fluidity. The silica attaches to the surface of each particle of the material, and functions like ball bearings because of its small size, enhancing fluidity of the material and contributing to uniform dispersion of the material, thus permitting stains in the device due to scattering of the toner to be reduced, and superior printing performance without fogging to be exhibited.

Description

【発明の詳細な説明】 〔発明の概要〕 電荷付与剤と疎水性シリカを混合段結着樹脂を混入し、
その後溶融混練して製造した電子写真用トナーであって
、かぶりとト十−飛(111,を低減さ一仕る。
[Detailed Description of the Invention] [Summary of the Invention] A charge imparting agent and hydrophobic silica are mixed in a stage in which a binder resin is mixed,
The toner for electrophotography is manufactured by melting and kneading the toner, which reduces fog and toner fly (111).

〔産業上の利用分野〕[Industrial application field]

本発明は電子写真用トナーに係り、特にかぶりが少なく
またトナー飛散が少ない電子写真用トナーに関する。
The present invention relates to an electrophotographic toner, and more particularly to an electrophotographic toner with less fog and less toner scattering.

〔従来の技術と問題点〕[Conventional technology and problems]

従来の電子写真用トナーしl電1i:i (・IIj剤
、結着樹脂、着色剤等の材ネ1を細かく↑5)砕し、適
ゝ11な混合比で混合し攪拌後、ニーダ博のIIII熱
γ+−(、練器ご溶融混合し冷却後、粉砕分級すること
により製造されていた。しかしながら」1記溶融(11
合(加熱混練)時に結着樹脂中での電荷H’j刑の分散
性が悪いと、冷却後粉砕分級したトナー個々6Z、l、
り電荷(J”P剤の量のばらつきを生じる。このトす・
−個々によるトナー比電荷のばらつきのため、かぶりや
トナー飛散が起こりやすくなる。加熱lIi練時の結着
樹脂  ′の粘度は高いため、電荷付与剤を均一に分散
させることはと困テ11であった。
Conventional toner for electrophotography (I finely crush the materials such as IIj agent, binder resin, coloring agent, etc. ↑5), mix at an appropriate mixing ratio, stir, and then mix. It was produced by melting and mixing in a kneader, cooling, and then crushing and classifying.
If the dispersibility of the charge H'j in the binder resin is poor during mixing (heating and kneading), the individual toner particles 6Z, l,
This causes a variation in the amount of J”P agent.
- Fogging and toner scattering are likely to occur due to variations in toner specific charge depending on the individual toner. Since the viscosity of the binder resin ' during heating lIi kneading was high, it was difficult to uniformly disperse the charge imparting agent11.

そこで本発明は電荷付与剤を結着樹脂中に均一に分散さ
せ、トナー比電荷のばらつきを少なくし、■つかふりと
トナー飛散が少ない電子写真用トナーを1是供すること
を目的とする。
Therefore, an object of the present invention is to uniformly disperse a charge-imparting agent in a binder resin, to reduce variations in toner specific charge, and to provide an electrophotographic toner with less scattering and toner scattering.

〔問題点を解決するだめの手段〕[Failure to solve the problem]

]−記問題点は本発明によれば、電荷付与剤と疎水1?
1シ11力を混合後、結着樹脂を混入し、その後該電イ
;;百・1与剤、疎水性シリカ及び結着樹脂を熔融混練
してなることを特徴とする電子写真用トナーに、lミっ
て解決される。
] - According to the present invention, the problem is that the charge imparting agent and the hydrophobic 1?
A toner for electrophotography, characterized in that after mixing 1 and 11 parts, a binder resin is mixed therein, and then the particulate material, hydrophobic silica, and a binder resin are melt-kneaded. , lmi is solved.

すなわち本発明は5μm以下に粉砕した電荷付与剤に疎
水性シリカを混合することにより電荷付り、剤の凝集が
解け、流動性が良くなることを利用し、電荷付与剤を結
着樹脂粉末中に均一に分散するようにしたものである。
In other words, the present invention takes advantage of the fact that by mixing hydrophobic silica with a charge imparting agent pulverized to 5 μm or less, it is charged, the agent is deagglomerated, and fluidity is improved, and the charge imparting agent is mixed into a binder resin powder. It is made to be uniformly dispersed.

この場合、疎水性シリカは電荷付与剤個々の表面に付着
し、粒径が小さいのでボール・\ブランクの様な働きを
するため電前付与剤の流動性が向上し均−分11れこ寄
tjするものと考えられる。
In this case, the hydrophobic silica adheres to the surface of each charge imparting agent, and since its particle size is small, it acts like a ball/blank, improving the fluidity of the charge imparting agent and increasing the uniformity of the charge imparting agent. It is considered that

電子用トナーは通常鉄粉、フ丁→イI・などの担体物質
(キャリア)占〆昆61(れ、−1中り−J’ Jの摩
擦により帯電する。1ナー質甲あたりの帯電頃をトナー
比電荷と呼ふ。トナー比電荷;:jの低いトナーはキャ
リアとの静電気引力が小、\いため、現像器の中でキャ
リアと撹11゛中に−1−中リアがら^11れ、トナー
飛敗が起り、現像器周辺がl’jれる問題や印字背景部
に霧状にト→・−がイ・1着するがふり現象を起す問題
がある。一方、トナー比重6;iの高いトナーは印字濃
度を上げるのが渾しい問題がある。従ってトナー中にト
ナー比電荷の低いトナーと高いトナーが混在していると
上記のような問題を起こしやすいため、トナー比電荷の
ばらつきが小さいことが望まれる。
Electronic toner is usually charged by the friction of a carrier material (carrier) such as iron powder, etc. is called the toner specific charge.Toner with a low specific charge:: Since the electrostatic attraction with the carrier is small, the toner has a low electrostatic attraction with the carrier in the developing device. , there is a problem that the toner is blown away and the area around the developing device is l'j, and that a mist of T→・- is deposited on the printed background area, causing a smearing phenomenon.On the other hand, the toner specific gravity is 6; Toners with high toner ratios have the problem of making it difficult to increase the print density. Therefore, if toners with low toner specific charges and toners with high toner specific charges are mixed, the above problems are likely to occur, and the variation in toner specific charges is desired to be small.

ところでトナー比電荷のばらつきを測定する確かな方法
は現在知られていない。一般に1−りm−比電荷と呼ば
れているものは、1−リ′−、lL電(ilのばらつき
を無視した、トナー全体の1リ−一比重4::fの平均
値である。そこで本発明者らは、下記に示す方法でトナ
ー比電荷のばらつきを類推した。一般にトナーに電荷(
」与剤を添加すると第1図に示す様に、ト・ノー−比電
荷は電荷付与剤の添加量の増加にともない増加するが、
電荷付与剤の添加量がある値以上になるとトナー比電荷
が飽和する傾向がある。従ってトナー個々の中で電荷付
与剤がある量以に含まれるとトナー比電荷はほとんど高
くならないと考えられる。従って第2A図及び第2B図
に示す様にトナー個々の中で電荷付与剤の量のばらつき
が大きい場合、ばらつきが小さい場合に比べて、平均ト
ナー比電荷は小さくなる。以上の理由により、同一組成
のトナーの場合平均トナー比電荷を測定することにより
、トナー比電荷のばらつきを類推できる。
However, there is currently no known reliable method for measuring variations in toner specific charge. What is generally called the 1-ri m-specific charge is the average value of the 1-li-1 specific gravity 4::f of the entire toner, ignoring variations in the 1-li'- and IL charges. Therefore, the present inventors estimated the variation in toner specific charge using the method shown below.In general, toner has a charge (
As shown in Figure 1, when a charge imparting agent is added, the to-no-specific charge increases as the amount of the charge imparting agent increases;
When the amount of the charge imparting agent added exceeds a certain value, the toner specific charge tends to be saturated. Therefore, it is considered that when a charge imparting agent is contained in an individual toner in an amount exceeding a certain amount, the specific charge of the toner hardly becomes high. Therefore, as shown in FIGS. 2A and 2B, when the variation in the amount of charge imparting agent among individual toners is large, the average toner specific charge becomes smaller than when the variation is small. For the above reasons, in the case of toners having the same composition, by measuring the average toner specific charge, it is possible to infer variations in the toner specific charge.

実施例1 電荷付与剤としてニグロシン染料(オイルブラックBY
、オリエント化学工業@)を用い、ジェン゛  トミル
(PJM扮砕機、日本ニューマチソク工業@)で粉砕を
行い、Fiptm以ドのfi+’+白、−し2だ。次に
疎水1生シリカ(且RO5IL l7972、r1本ア
エl’:lジル(掬)を0.9g、ポリエチレン製の2
01ボツI・に入れ、さらにその中へ前記染料を:IO
+l I+ ?+h合し、30分間ボールミルを行った
。次に結着樹脂とし−ζエポキシ樹脂(エピクロン40
60、人「1本インキ化学工業■)を用い、ロートプレ
ックス粉砕器(アルビネ社)により粉砕後、ジェットミ
ルで再粉砕を行い20pm以下の粒子とした。次に疎水
性シリカを混合した染料300 g、前記エポキシ樹脂
粉末9400 g、新たにカーボンブランク(ブラノク
バールズし、キ中ボット社)  3001(をボットで
30分間ボールミルを行った。得られた?fX合物を+
00°Cに加熱した加圧式ニーダ(DIO−20、聞出
製作所)を用いて、1時間混練した。混練後冷却したト
ナー塊をロートプレックス粉砕器により0.1〜’1m
の粗トナーとした。得られたIll・ナーをジェットミ
ルを用いて微粉砕を行い、粉砕物を風力分級機(アルビ
ネ社)により分級し、>’+’を径5〜20μmのトナ
ーを得た。このl・ナーと一1’−pリアとして鉄紛(
fil?V250、日本鉄粉製)とからなる現像剤をト
ナー濃度4呵%で調整し、F−671500レーザプリ
ンタ(富士jm製)を用いて印刷を行った。なおこの時
のトナー比電荷は16μc/gであった。印字試験の結
果、10万シートまでかぶりのない鮮明な印字が得られ
ると同時にトナー飛散による装置内部の汚れもほとんど
見られなかった。
Example 1 Nigrosine dye (oil black BY) as a charge imparting agent
, Orient Kagaku Kogyo @), and pulverized with a Gento mill (PJM crusher, Nippon New Matisoku Kogyo @), and the results were fi+'+white and -2 below Fiptm. Next, add 0.9 g of hydrophobic 1 raw silica (RO5IL 17972, 1 bottle of Ael': 1 silica), 2 pieces of polyethylene
01, and then add the dye into it: IO
+l I+? +h and ball milled for 30 minutes. Next, as a binder resin - ζ epoxy resin (Epicron 40
60.Using a human "Ippon Ink Kagaku Kogyo■)", it was ground with a Rotoplex grinder (Albine), and then re-pulverized with a jet mill to obtain particles of 20 pm or less.Next, dye 300 mixed with hydrophobic silica was ground. g, 9,400 g of the above epoxy resin powder, and a new carbon blank (Branokbars, Kinakobot Co., Ltd.) 3001 (ball milled for 30 minutes using a bot. The obtained ?fX compound was
The mixture was kneaded for 1 hour using a pressure kneader (DIO-20, Todide Seisakusho) heated to 00°C. After kneading, the cooled toner mass is crushed into 0.1 to 1 m by a Rotoplex pulverizer.
The coarse toner was prepared as follows. The obtained Ill toner was finely pulverized using a jet mill, and the pulverized product was classified using an air classifier (Albine Co., Ltd.) to obtain a toner with a diameter of 5 to 20 μm. This l・ner and 1′-p rear are iron powder (
fil? A developer consisting of V250 (manufactured by Nippon Steel Powder) was adjusted to a toner concentration of 4%, and printing was performed using an F-671500 laser printer (manufactured by Fuji JM). Note that the toner specific charge at this time was 16 μc/g. As a result of the printing test, clear printing without fogging was obtained up to 100,000 sheets, and at the same time, there was almost no staining inside the device due to toner scattering.

実施例2 疎水性シリカとしてN1psil 5S−50(ロ本シ
リカT業■)を使用し、他は実施例1と同様にトナーを
試イ1し、印字試験を行った。その結果、実施例1と同
様であった。
Example 2 A printing test was conducted using N1psil 5S-50 (Rohon Silica T-gyo ■) as the hydrophobic silica, and using a toner in the same manner as in Example 1 except for the above. The results were the same as in Example 1.

実施例3 疎水性シリカとしてAERO5IL R8]1 (日本
アエロジル(■)を使用し、他は実施例1と同様にトナ
ーを試作し、印字試験を行った。その結果、実施例1と
同様であった。
Example 3 A toner was prototyped in the same manner as in Example 1 except that AERO5IL R8]1 (Nippon Aerosil (■)) was used as the hydrophobic silica, and a printing test was conducted.The results were the same as in Example 1. Ta.

比較例I Vl水1ソ1ンリカを使用せず、他は実施例1と同様に
トナーを試作した。
Comparative Example I A toner was experimentally produced in the same manner as in Example 1 except that no liquid was used.

比較例2 実施例1で使用したニグロシン染料の粒径が10μm以
下(5μm以」二のものを含む)であること以外は実施
例1と同様にトナーを試作した。
Comparative Example 2 A toner was produced in the same manner as in Example 1, except that the particle size of the nigrosine dye used in Example 1 was 10 μm or less (including 5 μm or more).

比較例3 エポキシ樹脂(エピクロン7IO[io、大日本インキ
化学工業■製)301zm以下(2071m以]−のも
のを含む)に粉砕したものを用いたこと以外は実施例1
と同様にトす・−を試作した。
Comparative Example 3 Example 1 except that an epoxy resin (Epicron 7IO [io, manufactured by Dainippon Ink & Chemicals, Ltd.) pulverized into 301 zm or less (including 2071 m or more] -) was used.
In the same way, we made a prototype of Tosu・-.

比較例4 溶融混練前にあらかしめエボー1−シ樹脂(エピクロン
4060)とニゲ1:Iシン染才こ1をl昆合攪t’l
’しないこと以外は実施例1と同様にトす・−を試作し
た。
Comparative Example 4 Before melt-kneading, mix and mix Evo 1-shi resin (Epicron 4060) and Nige 1:I Shin Somesaiko 1.
A prototype was made in the same manner as in Example 1, except that the test was not carried out.

比較例で試作した4種類の1・J−一の1し電荷と印字
試験の結果をF記に示す。
Table F shows the results of four types of 1/J-1 1/1 charges and printing tests produced as comparative examples.

以上の結果より、比較例4種類のトナーは実施例2種類
のトナーに比べてトナー比電荷が低いことがわかった。
From the above results, it was found that the toners of the four types of comparative examples had lower toner specific charges than the toners of the two types of examples.

トナー組成は実施例、比較例とも同じことから、比較例
の方が電荷付与剤の分散性が悪いためと類)1Fできる
Since the toner composition is the same in both Examples and Comparative Examples, the dispersibility of the charge-imparting agent in Comparative Examples is poorer.

〔発明の効果〕〔Effect of the invention〕

以ト述説明したように本発明によればトナー比電荷のば
らつきを小さくすることができるので、トナー飛散によ
る装置内部の汚れが少なく、またかぶりのない優れた印
字性能を発揮することができる。
As explained above, according to the present invention, it is possible to reduce the variation in toner specific charge, so that there is less dirt inside the device due to toner scattering, and excellent printing performance without fogging can be exhibited.

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

第1図は電荷イ」与剤の添加量とトナー比電荷の関係を
示すグラフであり、第2A図は電荷付与剤の含有l、と
トナー個数の関係を示すグラフであり、第2B図はトナ
ー比電荷とトナー個数の関係を示すグラフである。 電荷付与剤の添加量 第1図 電荷付与剤の含有量 第2A図
FIG. 1 is a graph showing the relationship between the amount of charge imparting agent added and the specific charge of the toner, FIG. 2A is a graph showing the relationship between the charge imparting agent content l and the number of toner particles, and FIG. 2B is a graph showing the relationship between the amount of charge imparting agent added and the toner specific charge. 7 is a graph showing the relationship between toner specific charge and the number of toner particles. Addition amount of charge imparting agent Figure 1 Content of charge imparting agent Figure 2A

Claims (1)

【特許請求の範囲】 1、電荷付与剤と疎水性シリカを混合後、結着樹脂を混
入し、その後該電荷付与剤、疎水性シリカ及び結着樹脂
を溶融混練してなることを特徴とする電子写真用トナー
。 2、前記電荷付与剤の粒径が5μm以下であることを特
徴とする特許請求の範囲第1項記載の電子写真用トナー
。 3、前記疎水性シリカの粒径が1μm以下であることを
特徴とする特許請求の範囲第1項記載の電子写真用トナ
ー。 4、前記結着樹脂の粒径が20μm以下であることを特
徴とする特許請求の範囲第1項記載の電子写真用トナー
[Claims] 1. A charge imparting agent and hydrophobic silica are mixed, a binder resin is mixed therein, and then the charge imparting agent, hydrophobic silica, and binder resin are melt-kneaded. Toner for electrophotography. 2. The electrophotographic toner according to claim 1, wherein the charge imparting agent has a particle size of 5 μm or less. 3. The electrophotographic toner according to claim 1, wherein the hydrophobic silica has a particle size of 1 μm or less. 4. The electrophotographic toner according to claim 1, wherein the binder resin has a particle size of 20 μm or less.
JP60258475A 1985-11-20 1985-11-20 Electrophotographic toner Pending JPS62119548A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60258475A JPS62119548A (en) 1985-11-20 1985-11-20 Electrophotographic toner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60258475A JPS62119548A (en) 1985-11-20 1985-11-20 Electrophotographic toner

Publications (1)

Publication Number Publication Date
JPS62119548A true JPS62119548A (en) 1987-05-30

Family

ID=17320735

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60258475A Pending JPS62119548A (en) 1985-11-20 1985-11-20 Electrophotographic toner

Country Status (1)

Country Link
JP (1) JPS62119548A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01200368A (en) * 1988-02-05 1989-08-11 Sharp Corp Production of toner
JPH03157670A (en) * 1989-11-16 1991-07-05 Tomoegawa Paper Co Ltd Electrophotographic dry toner

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01200368A (en) * 1988-02-05 1989-08-11 Sharp Corp Production of toner
JPH03157670A (en) * 1989-11-16 1991-07-05 Tomoegawa Paper Co Ltd Electrophotographic dry toner

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