JPS6280668A - Developer for electrophotography - Google Patents

Developer for electrophotography

Info

Publication number
JPS6280668A
JPS6280668A JP60222212A JP22221285A JPS6280668A JP S6280668 A JPS6280668 A JP S6280668A JP 60222212 A JP60222212 A JP 60222212A JP 22221285 A JP22221285 A JP 22221285A JP S6280668 A JPS6280668 A JP S6280668A
Authority
JP
Japan
Prior art keywords
developer
pigment
added
particle size
aggregate
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
JP60222212A
Other languages
Japanese (ja)
Inventor
Masataka Sakaeda
栄田 正孝
Hideaki Yamashita
英明 山下
Kiichiro Tanaka
田中 喜一郎
Norihide Sato
典秀 佐藤
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP60222212A priority Critical patent/JPS6280668A/en
Publication of JPS6280668A publication Critical patent/JPS6280668A/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
    • G03G9/0802Preparation methods
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/0802Preparation methods
    • G03G9/081Preparation methods by mixing the toner components in a liquefied state; melt kneading; reactive mixing
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/0802Preparation methods
    • G03G9/0815Post-treatment
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G9/00Developers
    • G03G9/08Developers with toner particles
    • G03G9/0802Preparation methods
    • G03G9/0817Separation; Classifying

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Developing Agents For Electrophotography (AREA)

Abstract

PURPOSE:To shorten the time for heat fixing and to lower the temp. of heat fixing by flocculating primary particles having a specific grain size to form flocs having a specific grain size, thereby upgrading the sharpness of recorded characters and drawings. CONSTITUTION:35wt% Polyester resin, 55wt% tri-iron tetroxide and 10wt% carbon black as a pigment are mixed and the mixture is kneaded at 150 deg.C and is cooled to solidify. The cooled mixture is crushed by a hammer mill and is put into a ball mill made of Ni. After water is added to the powder, Ni balls are put therein and the powder is subjected to wet grinding. A soln. of a PE glycol is added to such suspension and the mixing is further continued for about 5 hours; thereafter, the suspension is subjected to drying, bonding the flocculating by a spray dryer. The dried powder is classified by spray classification to 3-15mum flocs.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、電子写真法を利用した電子式複写機、レーザ
ー記録式プリンタ、光プリンタ等の複写機や記録機に用
いられ、紙やプラスチック等の記録媒体上に文字や図面
等の可視像を形成するための電子写真用現像剤に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is used in copying machines and recording machines, such as electronic copying machines, laser recording printers, and optical printers, that utilize electrophotography, and is applicable to paper, plastic, etc. The present invention relates to an electrophotographic developer for forming visible images such as characters and drawings on a recording medium.

従来の技術 従来の現像剤としては特公昭58−40182号公報や
特開昭55−126266号公報に示されるように、熱
可塑性樹脂や磁性粉末や顔料等を混合した後に加熱して
熱固体化した後で粉砕して、3〜20μmの大きさにし
たものがある。また、その後表面処理をして球状化した
現像剤もある。
Conventional technology As shown in Japanese Patent Publication No. 58-40182 and Japanese Patent Application Laid-open No. 55-126266, conventional developers are made by mixing thermoplastic resins, magnetic powders, pigments, etc. and then heating to thermally solidify the mixture. After that, it is crushed to a size of 3 to 20 μm. Additionally, there is also a developer that is subsequently surface-treated to become spheroidal.

発明が解決しようとする問題点 しかしながらこれらの方法で製造された現像剤は、次の
ような問題点を有する。
Problems to be Solved by the Invention However, the developers produced by these methods have the following problems.

30粒子の大きさが、3〜20μmと大きくばらついて
いる。
The size of the 30 particles varies widely, ranging from 3 to 20 μm.

b、また平均粒子径が10〜15μmである。b, and the average particle diameter is 10 to 15 μm.

aの要因により、形成された文字が不鮮明になり、一般
にぼやけるような現像状態になる。これは、粒径やばら
つきが大きいためであり、また大きい粒子により現像さ
れた部分と小さい粒子により現像された部分では、当然
ながらその部分に存在する粒子数や現像した場合のトナ
ーの厚みも異なるためである。また、bの要因において
は、現像後、熱定着する段階において、定着の速度が現
像剤の粒径が大きいために70mm/sec以下となり
、高速化できないし、熱定着の温度も高くなる。これは
次のような理由による。
Due to the factor a, the formed characters become unclear and are generally developed in a blurred state. This is because the particle size and variation are large, and the number of particles existing in that area and the thickness of the toner when developed are naturally different between areas developed with large particles and areas developed with small particles. It's for a reason. Regarding factor b, in the step of thermal fixing after development, the fixing speed is less than 70 mm/sec due to the large particle size of the developer, which makes it impossible to increase the speed and also increases the temperature of thermal fixing. This is due to the following reasons.

粒子径が大きいものと小さいものでは、表面エネルギー
は、小さいものが大きい。つまり反応しやすい。また、
熱定着の現象は現像剤粒子が、特に現像剤粒子中の熱可
塑性樹脂部が、温度の上昇に伴って融解し、紙の繊維部
等と融着、もしくは接着し、且つ現像剤粒子同志も融着
して終了する過程である。従って、この現象は粒子径が
小さいもの程良いことになる。
When it comes to particles with large and small particle sizes, the smaller the particle size, the larger the surface energy. In other words, it is easy to react. Also,
The phenomenon of heat fixation is that the developer particles, especially the thermoplastic resin part in the developer particles, melt as the temperature rises and fuse or adhere to the paper fibers, etc., and the developer particles also melt with each other. This is a process that ends with fusing. Therefore, the smaller the particle size, the better this phenomenon will be.

問題点を解決するための手段 本発明は0.3〜1.0μmの粒径を有する一次粒子を
凝集させて粒径が3〜15μmの凝集体としたものであ
る。
Means for Solving the Problems In the present invention, primary particles having a particle size of 0.3 to 1.0 μm are aggregated to form an aggregate having a particle size of 3 to 15 μm.

作用 上記手段を用いることにより、記録された文字や図面の
鮮明度が上昇し、且つ熱定着の時間の短縮化、熱定着の
温度の低温化が可能になる。
Effect: By using the above means, the clarity of recorded characters and drawings can be increased, and it is also possible to shorten the heat fixing time and lower the heat fixing temperature.

実施例 以下、本発明の一実施例について説明する。Example An embodiment of the present invention will be described below.

〈実施例1〉 ポリエステル樹脂35wt%と、四三酸化鉄55wt%
と、顔料としてカーボンブラックLowt%を混合し、
次に150℃にて混練して冷却し、固体化した。次に、
これをハンマーミルで粗粉砕し、さらにNi製のボール
ミルに入れ、水を添加した後、Niポールを入れて湿式
粉砕を行った。200時間経過したところで、黒色に懸
濁した液を約10cc取り出し、これを粒度分布測定器
にかけたら、1μm以下であった。さらに、電子顕微鏡
で測定してみても、直径1μm以上はみられず、はとん
どが0.6μm程度であった。この懸濁液に、ポリエチ
レングリコールの溶液を添加して、さらに5時間程度混
合を続けた。その後、この懸濁液をスプレードライヤー
にて、乾燥と結合凝集化させた。さらに、これを噴霧分
級により、3〜15μmの凝集体となるように分級した
。このようにして、本発明の電子写真用現像剤を作成し
た。
<Example 1> 35 wt% polyester resin and 55 wt% triiron tetroxide
and carbon black Lowt% as a pigment,
Next, the mixture was kneaded at 150°C, cooled, and solidified. next,
This was coarsely pulverized with a hammer mill, then placed in a Ni ball mill, water was added, and a Ni pole was placed there for wet pulverization. After 200 hours had elapsed, about 10 cc of the black suspended liquid was taken out and applied to a particle size distribution analyzer, and the particle size was 1 μm or less. Furthermore, even when measured using an electron microscope, no diameter of 1 μm or more was observed, and most of the diameters were about 0.6 μm. A polyethylene glycol solution was added to this suspension, and mixing was continued for about 5 hours. Thereafter, this suspension was dried and coagulated using a spray dryer. Furthermore, this was classified into aggregates of 3 to 15 μm by spray classification. In this way, an electrophotographic developer of the present invention was prepared.

次に、この現像剤をコピー装置に入れて一辺4備の正方
形で、線幅1mm、0.5mm、0.2mmの3種類を
描かせて、従来の現像剤との鮮明度を比較した。比較方
法は50倍の顕微鏡で描がれた線の直線性で判断した。
Next, this developer was placed in a copying machine, and three types of line widths, 1 mm, 0.5 mm, and 0.2 mm, were drawn on a square with 4 lines on each side, and the sharpness was compared with that of a conventional developer. The comparison method was determined by the linearity of a line drawn using a 50x microscope.

その結果、本発明の現像剤の方が優れていた。As a result, the developer of the present invention was superior.

更に熱定着の時間および温度については、同様の図形を
コピーし、熱定着の時間および温度を変化させて行った
。熱定着の時間はヒーターロールの速度にて判断し、温
度はヒーターロールの温度にて判断した。
Further, regarding the heat fixing time and temperature, similar shapes were copied and the heat fixing time and temperature were varied. The heat fixing time was determined by the speed of the heater roll, and the temperature was determined by the temperature of the heater roll.

そして、評価は前記図形の上をプラスチック消しゴムで
荷重100 g / cJを加えてこすり、これを10
回繰り返した後、消しゴムの汚れにより判断した。定着
が不十分であると、現像剤粒子が脱°離して、消しゴム
およびその脱離部分のゴムが黒く変色する。その結果、
従来の現像剤より熱定着速度を2倍以上に、同一の温度
のもとでは行うことができた。さらに、温度は20℃低
減することができた。また、レーザープリンタや光プリ
ンタにも用いることができた。そこで、凝集体の粒径と
顕微鏡下での線の鮮明度との関係を調べてみた。3〜1
5μmの凝集粒径をもつ現像剤と、15〜25μm凝集
粒径をもつ現像剤とを用いて、コピー装置にて文字およ
び図面を印刷して見た結果、明らかに3〜15μmの場
合が鮮明であった。また、3μm未満では流動性が減少
して、磁気ロールによる回転流動化が悪くなった。
Then, the evaluation was performed by rubbing a plastic eraser on the shape with a load of 100 g/cJ.
After repeating the test several times, judgment was made based on the dirt on the eraser. If the fixing is insufficient, the developer particles will detach and the eraser and the rubber at the detached portion will turn black. the result,
The heat fixing speed was more than twice that of conventional developers at the same temperature. Furthermore, the temperature could be reduced by 20°C. It could also be used in laser printers and optical printers. Therefore, we investigated the relationship between the particle size of aggregates and the sharpness of lines under a microscope. 3-1
Using a developer with an aggregated particle size of 5 μm and a developer with an aggregated particle size of 15 to 25 μm, characters and drawings were printed using a copying machine, and it was clear that the cases with 3 to 15 μm were clearer. Met. Moreover, when the thickness is less than 3 μm, the fluidity decreases and rotational fluidization by the magnetic roll becomes poor.

以上の結果により、粒径は3〜15μmが良好である。According to the above results, a particle size of 3 to 15 μm is favorable.

また、−次粒子の製造はハンマーミルで粗粉砕した後、
ジェットミルで1μm以下の粒子としても同様の結果が
得られた。ジェットミルで粉砕して得た一次粒子をポリ
エチレングリコールの溶液中に懸濁した後、スプレード
ライヤーにて、凝集体化して現像剤とした。しかし、ジ
ェットミルでの一次粒子の収率は湿式法よりも悪かった
In addition, to produce secondary particles, after coarsely pulverizing with a hammer mill,
Similar results were obtained using a jet mill for particles of 1 μm or less. The primary particles obtained by pulverization with a jet mill were suspended in a polyethylene glycol solution, and then aggregated with a spray dryer to obtain a developer. However, the yield of primary particles in the jet mill was worse than that in the wet method.

第1図は、本発明の現像剤の構成を示す図である。ここ
で、1は磁性粉末、2は顔料、3は可熱塑性樹脂、4は
結合凝集剤である。
FIG. 1 is a diagram showing the structure of the developer of the present invention. Here, 1 is a magnetic powder, 2 is a pigment, 3 is a thermoplastic resin, and 4 is a binding flocculant.

結合凝集剤は、ポリアクリル系バインダーでも同様の結
果が得られた。ポリアクリル系バインダーは、水溶性の
ものであることが必要である。
Similar results were obtained using a polyacrylic binder as the binding flocculant. The polyacrylic binder needs to be water-soluble.

〈実施例2〉 実施例1と同様の方法を用いて、組成範囲を調べた。熱
化塑性樹脂は、色調が薄いために顔料を添加して色調を
濃くする必要がある。また、磁性粉末は顔料程もないに
しても、赤黒色の色調を有する。そこで、磁性粉末を5
0wt%一定として、顔料を添加した時の効果を調べた
。その結果を表−1に示した。
<Example 2> Using the same method as in Example 1, the composition range was investigated. Thermoplastic resins have a pale color, so it is necessary to add pigments to make them darker. In addition, the magnetic powder has a reddish-black color tone, although it is not as strong as that of the pigment. Therefore, we added 50% of magnetic powder.
The effect of adding a pigment was investigated with the amount constant at 0 wt%. The results are shown in Table-1.

表−1 また、磁性粉末を60wt%一定とした時の場合を表−
2に示した。
Table-1 Also, Table-1 shows the case when the magnetic powder is kept constant at 60wt%.
Shown in 2.

表−2 濃度は、コピー装置にて印刷した時の、文字の色調を目
視によって判断した。色調は、5wt%と20wt%と
はほとんど変化がなく、18wt%以上顔料を配合して
も効果はなく、経済的優位性を欠くことになる。顔料は
、カーボンブラックを用いた。ニグロシンを用いても同
様の結果が得られた。
Table 2 Density was determined by visually observing the color tone of characters when printed using a copying machine. There is almost no difference in color tone between 5 wt % and 20 wt %, and even if 18 wt % or more of pigment is added, there is no effect and it lacks economic advantage. Carbon black was used as the pigment. Similar results were obtained using nigrosine.

現像剤の磁性粉末の含有率と、現像時の文字の鮮明度と
の関係を調べた。現像剤の現像条件を−。
The relationship between the content of magnetic powder in the developer and the clarity of characters during development was investigated. - Development conditions for the developer.

定にするために第2図のようにスリーブ付のマグネット
ロールを用いて、マグネットロールを140Orpmで
回転させ、且つスリーブを同方向に15Orpmで回転
し、さらに現像剤規制用のドクターブレードの間隔を0
.4mmとして行った。
In order to maintain this level, a magnetic roll with a sleeve is used as shown in Figure 2, and the magnetic roll is rotated at 140 Orpm, and the sleeve is rotated in the same direction at 15 Orpm, and the interval between the doctor blades for regulating the developer is adjusted. 0
.. The diameter was set to 4 mm.

顔料を5 w t%一定とした場合の結果を表−3に示
す。第2図において5はドクターブレード、6はスリー
ブ、7はマグネットロール、8は現像剤である。
Table 3 shows the results when the pigment content was constant at 5 wt%. In FIG. 2, 5 is a doctor blade, 6 is a sleeve, 7 is a magnet roll, and 8 is a developer.

表−3 また、顔料を15wt%一定とした場合を表−4に示す
Table 3 In addition, Table 4 shows the case where the pigment was kept constant at 15 wt%.

表−4 このように、磁性粉末の含有率が低い時に、鮮明さが劣
化するのは磁性粉末の含有率が低いために現像剤の磁気
力が弱くなって、少し横の方へもちらぼるためと考えら
れる。静電潜像の帯電量およびそれに誘起される電気力
により引き寄せられる現像剤は、磁気力により固着され
ているが、磁気力が弱ければ少ない帯電の潜像の所にも
引き寄せられて、現像時に鮮明度が劣化するわけである
Table 4 As shown above, when the content of magnetic powder is low, the sharpness deteriorates because the magnetic force of the developer becomes weak due to the low content of magnetic powder, and it also scatters slightly to the side. It is thought that this is because of this. The developer, which is attracted by the amount of charge on the electrostatic latent image and the electric force induced by it, is fixed by magnetic force, but if the magnetic force is weak, it will be attracted to the less charged latent image, and during development. The sharpness deteriorates.

以上の結果より、磁性粉末は最低50wt%必要である
ことがわかる。
From the above results, it can be seen that a minimum amount of magnetic powder of 50 wt% is required.

次に熱可塑性樹脂の含有率による熱定着の程度を調べた
。その結果を表−5に示した。その評価は実施例1にお
いて、消しゴムにて評価した方法を用いた。条件は、ヒ
ートロール速度を140ma/ s e c 、ヒート
ロール温度を150℃として行った。顔料を5 w t
%とした場合を表−5に示す。
Next, the degree of heat fixation was investigated depending on the content of thermoplastic resin. The results are shown in Table-5. The evaluation was performed using the method of evaluating using an eraser in Example 1. The conditions were a heat roll speed of 140 ma/sec and a heat roll temperature of 150°C. 5 wt pigment
Table 5 shows the percentage.

表−5 また、表−6に顔料を15wt%とした場合を示す。Table-5 Further, Table 6 shows the case where the pigment was 15 wt%.

表−6 熱可塑性樹脂は、ポリエステル、ポリアミド。Table-6 Thermoplastic resins include polyester and polyamide.

ポリスチレン、ポリエチレン、スチレンアクリル共重合
体、エチレン酢酸ビニル共重合体について行った。すべ
てにおいて同様の結果が得られた。
The tests were conducted on polystyrene, polyethylene, styrene-acrylic copolymer, and ethylene-vinyl acetate copolymer. Similar results were obtained in all cases.

以上の結果により、顔料は5 w t%以上が必要であ
り、磁性粉末は50 w t%以上必要であることがわ
かる。また、熱可塑性樹脂は35wt%以上必要である
。従って、実験の結果から熱可塑性樹脂35〜45 w
 t%、磁性体粉末50〜60wt%、顔料5〜15w
t%が、本発明の組成配合比である。
From the above results, it can be seen that 5 wt% or more of the pigment is required, and 50 wt% or more of the magnetic powder is required. Further, the thermoplastic resin is required to be at least 35 wt%. Therefore, from the experimental results, thermoplastic resin 35 to 45 w
t%, magnetic powder 50-60wt%, pigment 5-15w
t% is the composition ratio of the present invention.

さらに結合凝集剤の添加量を調べた。上記組成の一次粒
子中に、ポリエチレングリコールの溶液を添加し、スプ
レードライヤーで凝集体化させた現像剤の凝集粒径、お
よび50℃の温度における固体化の状況を調べた。
Furthermore, the amount of binding flocculant added was investigated. A solution of polyethylene glycol was added to the primary particles of the above composition, and the agglomerated particle size of the developer was aggregated using a spray dryer, and the state of solidification at a temperature of 50° C. was investigated.

凝集体粒径において、粒径はその90%以上の粒子の粒
径をもって、平均粒径とした。
Regarding the particle size of the aggregate, the particle size of 90% or more of the particles was defined as the average particle size.

第3図は、結合凝集剤の添加率と平均粒径との関係を調
べた結果を示す。
FIG. 3 shows the results of investigating the relationship between the addition rate of the binding flocculant and the average particle size.

また、添加率と50℃における固体化の状況を調べた。Additionally, the addition rate and solidification status at 50°C were investigated.

固体化とは、現像剤がその粒子同志が反応して結合し大
きな団粒となることである。その結果を表−7に示す。
Solidification means that particles of the developer react with each other and combine to form large aggregates. The results are shown in Table-7.

団粒化は、粒子同志が50℃の温度にて4000時間経
過しても団粒化するかどうかで調べた。
Agglomeration was examined by determining whether the particles remained agglomerated even after 4000 hours at a temperature of 50°C.

表−7 以上の結果より、結合凝集剤は1〜3wt%が良いこと
になる。
Table 7 From the above results, it is found that 1 to 3 wt% of the binding flocculant is good.

また、磁性粉末は四三酸化鉄以外に、Mn−ZUフェラ
イト、鉄粉を用いて行ったが、同様の結果が得られた。
In addition, Mn-ZU ferrite and iron powder were used as the magnetic powder in addition to triiron tetroxide, but similar results were obtained.

磁性粉末は軟磁性体材料であり、現像剤が一定の透磁率
を持つようなものであれば何でもよいと考えられる。
The magnetic powder is a soft magnetic material, and any powder may be used as long as the developer has a certain magnetic permeability.

〈実施例3〉 陽極性現像剤とするために、本発明の凝集体にニグロシ
ン系の電子供与性染料を1 w t%荷電制御剤として
添加し、且つ流動化剤としてコロイダルシリカを1 w
 t%、クリーニング剤としてフッ素系界面活性剤を1
 w t%添加した。そして混合を行った。これを用い
て複写を行った結果、鮮明な複写が行われた。
<Example 3> To prepare an anodic developer, 1 wt% of a nigrosine-based electron-donating dye was added as a charge control agent to the aggregate of the present invention, and 1 w of colloidal silica was added as a fluidizing agent.
t%, 1 fluorine surfactant as a cleaning agent
wt% was added. Then, mixing was performed. As a result of copying using this, clear copies were made.

また、上記の荷電制御剤を3 w t%、流動化剤を3
 w t%、クリーニング剤を3 w t%を添加した
結果、同様な鮮明な複写が行えた。
In addition, the above charge control agent was added at 3 wt%, and the fluidizing agent was added at 3 wt%.
As a result of adding 3 wt% of the cleaning agent, similar clear copies could be made.

さらに、負極性現像剤とするために、銅フタロシアニン
系化合物を荷電制御剤として加えた。その比率は、前記
陽極性現像剤に加えた荷電制御剤の場合と同じである。
Furthermore, a copper phthalocyanine compound was added as a charge control agent to obtain a negative polarity developer. The ratio is the same as in the case of the charge control agent added to the anodic developer.

その結果、良好な負極性現像剤として作用し、良好な複
写が行えた。
As a result, it acted as a good negative polarity developer and good copying was possible.

また、レーザープリンタや光プリンタ用の現像剤として
も、十分用いることができた。
It could also be used satisfactorily as a developer for laser printers and optical printers.

発明の効果 本発明の電子写真用現像剤を用いることにより、鮮明な
複写、もしくは記録が行え、且つ熱定着の速さを7cm
/secで行うことができ、熱定着の温度を5℃と低減
することが可能になった。
Effects of the Invention By using the electrophotographic developer of the present invention, clear copying or recording can be performed, and the heat fixing speed can be increased to 7 cm.
/sec, making it possible to reduce the heat fixing temperature to 5°C.

従って、記録、あるいは複写の高速化を実現することが
できる。
Therefore, it is possible to realize faster recording or copying.

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

第1図は本発明の電子写真用現像剤を模式的に示す図、
第2図は現像剤とマグネットロールとの関係を説明する
ための断面図、第3図は結合凝集剤の添加率と凝集体の
平均粒系との関係を示す図である。 1・・・・磁性粉末      2・・・・顔  料3
・・・・熱可塑性樹脂    4・・・・結合凝集剤代
理人の氏名 弁理士 中尾敏男 ほか1名f−7か1粉
釆 4、−−jit Jtlh 第 3 図 斎゛L“+)綻果 1ゴ シ贋ト刀B  q   (w
t z)手続補正書 昭和61年 2月 77日 1 事件の表示 昭和60年特許願第 222212  号2 発明の名
称 電子写真用現像剤 3 補正をする者 事件との関係  特 許 出 願 大 佐 所  大阪府門真市大字門真1006番地名 称 
’(582)  松下電器産業株式会社代表者    
  山  下  俊  彦4代理人 〒571 住 所  大阪府門真市大字門真1006番地松下電器
産業株式会社内 氏名 (,5971)  弁理土中尾敏男(ほか1名) [連絡先 電話(東京) 437−1121  東京法
務分室15 補正の対象 明細書の発明の詳細な説明の欄 6 補正の内容 (1)  明細書の第12頁の表−7を以下のように補
正します。 「 表−7
FIG. 1 is a diagram schematically showing the electrophotographic developer of the present invention,
FIG. 2 is a cross-sectional view for explaining the relationship between the developer and the magnet roll, and FIG. 3 is a diagram showing the relationship between the addition rate of the binding flocculant and the average particle system of the aggregates. 1...Magnetic powder 2...Pigment 3
... Thermoplastic resin 4... Name of agent for binding flocculant Patent attorney Toshio Nakao and one other person f-7 or 1 powder pot 4, --jit Jtlh No. 3 1 go counterfeit sword B q (w
t z) Procedural amendment February 77, 1988 1 Indication of the case 1985 Patent Application No. 222212 2 Name of the invention Electrophotographic developer 3 Relationship with the person making the amendment Patent application Colonel Osaka 1006 Kadoma, Fukadoma City
'(582) Representative of Matsushita Electric Industrial Co., Ltd.
Toshihiko Yamashita 4 Agent 571 Address Matsushita Electric Industrial Co., Ltd., 1006 Oaza Kadoma, Kadoma City, Osaka Name (,5971) Patent attorney Toshio Tsuchinakao (and 1 other person) [Contact information Telephone (Tokyo) 437-1121 Tokyo Legal Affairs Branch 15 Column 6 for Detailed Explanation of the Invention in the Specification Subject to Amendment Contents of Amendment (1) Table 7 on page 12 of the specification will be amended as follows. "Table-7

Claims (4)

【特許請求の範囲】[Claims] (1)比抵抗が10^1^2Ωcm以上の熱可塑性樹脂
と、四三酸化鉄の磁性粉末と、カーボンブラック、ニグ
ロシンを主とする顔料よりなる混合体で構成された一次
粒子の凝集体よりなり、且つ一次粒子は粒径が0.3μ
m〜1μmであり、上記凝集体は上記一次粒子をポリエ
チレングリコールやポリアクリル系バインダーを結合凝
集剤として凝集させた凝集体であり、且つ上記凝集体の
粒径が3μm〜15μmであることを特徴とする電子写
真用現像剤。
(1) From an aggregate of primary particles composed of a mixture of a thermoplastic resin with a specific resistance of 10^1^2 Ωcm or more, magnetic powder of triiron tetroxide, and pigments mainly containing carbon black and nigrosine. and the primary particle has a particle size of 0.3μ
m to 1 μm, and the aggregate is an aggregate obtained by aggregating the primary particles using polyethylene glycol or a polyacrylic binder as a binding flocculant, and the particle size of the aggregate is 3 μm to 15 μm. An electrophotographic developer.
(2)熱可塑性樹脂は、ポリエステル、ポリアミド、ポ
リスチレン、ポリエチレン、スチレンアクリル共重合体
、エチレン酢酸ビニル共重合体のいずれかであることを
特徴とする特許請求の範囲第1項記載の電子写真用現像
剤。
(2) For electrophotography according to claim 1, wherein the thermoplastic resin is any one of polyester, polyamide, polystyrene, polyethylene, styrene-acrylic copolymer, and ethylene-vinyl acetate copolymer. developer.
(3)磁性粉末50〜60wt%、熱可塑性樹脂35〜
45wt%、顔料5〜15wt%の配合比をもち、結合
凝集剤を1〜3wt%添加した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現像剤。
(3) Magnetic powder 50~60wt%, thermoplastic resin 35~
45 wt% of pigment, 5 to 15 wt% of pigment, and 1 to 3 wt% of a binding and aggregating agent.
(4)荷電制御剤1〜3wt%、流動化剤1〜3wt%
、クリーニング剤1〜3wt%を添加してなることを特
徴とする特許請求の範囲第1項記載の電子写真用現像剤
(4) Charge control agent 1-3 wt%, fluidizing agent 1-3 wt%
2. The electrophotographic developer according to claim 1, wherein 1 to 3 wt% of a cleaning agent is added.
JP60222212A 1985-10-04 1985-10-04 Developer for electrophotography Pending JPS6280668A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60222212A JPS6280668A (en) 1985-10-04 1985-10-04 Developer for electrophotography

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60222212A JPS6280668A (en) 1985-10-04 1985-10-04 Developer for electrophotography

Publications (1)

Publication Number Publication Date
JPS6280668A true JPS6280668A (en) 1987-04-14

Family

ID=16778888

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60222212A Pending JPS6280668A (en) 1985-10-04 1985-10-04 Developer for electrophotography

Country Status (1)

Country Link
JP (1) JPS6280668A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07199540A (en) * 1993-12-28 1995-08-04 Narumi China Corp Organic and inorganic composite powder for dry transfer and its production

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07199540A (en) * 1993-12-28 1995-08-04 Narumi China Corp Organic and inorganic composite powder for dry transfer and its production

Similar Documents

Publication Publication Date Title
JPS6332182B2 (en)
US5223365A (en) Magnetic toner
JPH0280A (en) Magnetic toner, negative chargeable one-component developer and image forming method
JPH083657B2 (en) Toner composition and method for producing the same
US5731121A (en) Developer for electrostatic latent image development
US5336580A (en) Carrier composition for electrophotography
JPS6280668A (en) Developer for electrophotography
JPS62269150A (en) Electrostatic charge image developing toner
JPS5823622B2 (en) Manufacturing method of magnetic toner for electrostatic photography
JPH04204658A (en) Electrophotographic one component system developer
JP4116694B2 (en) Magnetic toner for electrostatic latent image
JPS63228174A (en) Magnetic carrier and its manufacture
EP0559250B1 (en) Magnetic carrier particles
JPH07248638A (en) Electrophotographic toner
JPS5895748A (en) Transfer type magnetic toner particle
JPH0424705B2 (en)
JPS5838958A (en) Magnetic toner
JP2728954B2 (en) Magnetic toner for developing electrostatic latent images
JP4293885B2 (en) Electrostatic image developer
JP2567748B2 (en) Toner for electrostatic charge development
JPH04162051A (en) Insulating magnetic toner
JP3094678B2 (en) Electrophotographic method
JPS58187946A (en) Electrophotographic developer
JPS6355060B2 (en)
JPS6332382B2 (en)