JPS616656A - Developer - Google Patents
DeveloperInfo
- Publication number
- JPS616656A JPS616656A JP59125305A JP12530584A JPS616656A JP S616656 A JPS616656 A JP S616656A JP 59125305 A JP59125305 A JP 59125305A JP 12530584 A JP12530584 A JP 12530584A JP S616656 A JPS616656 A JP S616656A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- binder resin
- colored particles
- charge
- developing
- 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
Links
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/0821—Developers with toner particles characterised by physical parameters
- G03G9/0823—Electric parameters
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08795—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by their chemical properties, e.g. acidity, molecular weight, sensitivity to reactants
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/087—Binders for toner particles
- G03G9/08784—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775
- G03G9/08797—Macromolecular material not specially provided for in a single one of groups G03G9/08702 - G03G9/08775 characterised by their physical properties, e.g. viscosity, solubility, melting temperature, softening temperature, glass transition temperature
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の技術分野〕
本発明杖現像剤に関し、詳しくは電子写真装置又は静電
記録装置において、感光体もしくは誘電体上に形成され
た静電潜像を可視像化する一成分非磁性現像剤に係る。[Detailed Description of the Invention] [Technical Field of the Invention] The wand developer of the present invention is used to convert an electrostatic latent image formed on a photoreceptor or dielectric material into a visible image in an electrophotographic device or an electrostatic recording device. This relates to a one-component non-magnetic developer.
現像剤はトナーとキャリアからなる二成分現像剤が画質
のよいことから広範に用いられている。Two-component developers consisting of toner and carrier are widely used because of their good image quality.
しかしながら、その反面、以下に示すよりな二成分系の
現像剤に共通する欠点がある。すなわち、■トナーは、
トナーとキャリア間の相互摩擦によ)摩擦電荷を受けと
るのであるが、その場合、長期にわたシ使用してしると
、キャリア表面がトナーの組成物によって汚染され、そ
の結果、充分な電荷を獲得でき彦くなる。■トナーとキ
ャリアは所定範囲の混合比に調整されていなければなら
ないが、長期にわたり使用していると、その混合比が変
動して所定範囲から外れてし1う。■一般にキャリアと
しては表面を酸化した鉄粉若しくはガラスピーズが多用
されているが、その場合、これらキャリアによって感光
体の表面が機械的に損傷される。However, on the other hand, there are drawbacks common to two-component developers as shown below. In other words, ■toner is
After long-term use, the carrier surface becomes contaminated with the toner composition and, as a result, does not carry enough charge. I can get it and become Hiko. (2) The mixture ratio of toner and carrier must be adjusted within a predetermined range, but if used for a long period of time, the mixture ratio will fluctuate and deviate from the predetermined range. (2) Generally, iron powder or glass beads with oxidized surfaces are often used as carriers, but in this case, the surface of the photoreceptor is mechanically damaged by these carriers.
このようなことからトナーのみから成る一成分系の現像
剤を用いた各種の現像法が提巣されている。とシわけ、
感磁性を有し、一般に磁性トナーと呼ばれる現像剤を用
いた現像法が多数提案されているが1、それらのうち、
米国特許第3909258号、同第4121931号等
に基づくものが実用化されている。しかしながら、これ
らの方法にも次のような欠点がある。すなわち■比較的
比抵抗の小さい磁性トナーを用いるので、静電潜像上の
現像像を普通紙等の支持部材へ静電的に転写することが
固離であること、とシわけ、多湿の雰囲気下では充分な
転写が得られないこと、■トナーが多量の磁性粉を含有
するので、カラートナーが得られないこと、などの欠点
を有する。For this reason, various developing methods using a one-component developer consisting only of toner have been proposed. And so,
Many development methods have been proposed that use a developer that is magnetically sensitive and is generally called a magnetic toner.1 Among these,
Those based on US Pat. No. 3,909,258, US Pat. No. 4,121,931, etc. have been put into practical use. However, these methods also have the following drawbacks. In other words, ■Since magnetic toner with relatively low resistivity is used, electrostatic transfer of the developed image on the electrostatic latent image to a support member such as plain paper is solidification, and It has disadvantages such as insufficient transfer in an atmosphere, and (2) color toner cannot be obtained because the toner contains a large amount of magnetic powder.
しかるに、最近は、磁性粉を含有せず比抵抗の大きい一
成分系トナーを用いた現像法を特に注目を集めている。However, recently, a developing method using a one-component toner that does not contain magnetic powder and has a high specific resistance has been attracting particular attention.
それらの現像法としては、例えば、米国特許第2895
847号、同第3,152,012号、特公昭41−9
475号、同45−2877号、同54−3624号等
に記載されているタッチダウン法、インプレッション法
、ジャンピング法に基づくものがあげられる。これらの
方法では、二成分系に用いられていた従来のトナーを利
用している。Such developing methods include, for example, US Pat. No. 2,895
No. 847, No. 3,152,012, Special Publication No. 41-9
Examples include methods based on the touchdown method, impression method, and jumping method described in No. 475, No. 45-2877, and No. 54-3624. These methods utilize conventional toners used in two-component systems.
しかしながら、この場合、以下に述べるように、−成分
系に関連する種々の問題点の派生を避は得ない。However, in this case, various problems associated with the -component system are unavoidable, as described below.
第1の問題点は摩擦帯電9問題である。The first problem is the triboelectrification problem.
すなわち現像剤は現像剤担持体と効率よく、しかも極め
て短時間に感光体ドラムもしくは誘電体に形成された静
電潜像を非接触で可視像化するに必要な帯電量を得なけ
ればならない。しかるに、可視像化するに必要な現像剤
の現像剤と現像剤担持体とによる帯電量は、セレンの感
光体ドラムを用いた場合マイナス0.5〜15μC/p
である。In other words, the developer must efficiently interact with the developer carrier and obtain the amount of charge necessary to visualize the electrostatic latent image formed on the photoreceptor drum or dielectric material in a very short time without contact. . However, when a selenium photoreceptor drum is used, the amount of charge required by the developer and the developer carrier to visualize the image is -0.5 to 15 μC/p.
It is.
しかし、従来の二成分系に用いられた現像剤を用い、現
像剤担持体と現像剤によるFA擦帯電では可視像化する
に充分な帯電量が充分に得られない。However, using a developer used in a conventional two-component system, FA tribocharging using a developer carrier and the developer does not provide a sufficient amount of charge to visualize the image.
この理由として、従来の二成分系に用いられた現像剤は
、可視像化を形成するに必要なイ〃電量を得るに充分な
時間を要してトナーとキャリアとの摩擦帯電を行なって
いる。The reason for this is that developers used in conventional two-component systems require sufficient time to triboelectrically charge the toner and carrier to obtain the amount of charge necessary to form a visible image. There is.
しかし、帯電量が高いと地かぶりの原因となシうる為、
二成分現像剤の帯1!量を制御している。However, if the amount of charge is high, it may cause background fogging, so
Two-component developer band 1! The amount is controlled.
従来の二成分現像剤は、帯電力での小きい結シγ1樹脂
を主成分とし、帯電制御剤を添加することにより、IF
i量を制御している。Conventional two-component developers are mainly composed of γ1 resin, which exhibits small condensation under charging power, and by adding a charge control agent, IF
i amount is controlled.
しかし、帯電制御剤を多量に用いることは画像11ψ性
に影響を及ぼす為、二成分現1゛〕メ剤の帯電量は、主
成分である結着樹脂で決まる。However, since using a large amount of charge control agent affects the image quality, the amount of charge of the two-component developer is determined by the binder resin, which is the main component.
実験によると、第2図に図示した如く、A6着樹脂の帯
電量(ブローオフ法)は、結着樹脂の酸価(KOH法に
よる測定)と比例関係にある。第2図から明らかな様に
、酸価が低い結着樹脂は、帯電量も低い、一般に二成分
現像剤のブローオフ法による帯電量は10〜30μC/
yである。According to experiments, as shown in FIG. 2, the amount of charge of the A6 binder resin (blow-off method) is proportional to the acid value of the binder resin (measured by the KOH method). As is clear from Figure 2, a binder resin with a low acid value also has a low charge amount. Generally, the charge amount by the blow-off method of a two-component developer is 10 to 30 μC/
It is y.
又、現像剤のブローオフ法による帯電量と現像剤と現像
剤担持体による帯電量の関係を第3図に図示した。Further, FIG. 3 shows the relationship between the charge amount of the developer by the blow-off method and the charge amount of the developer and the developer carrier.
第3図から明らかな様に、二成分現像剤は現像剤と現像
剤担持体による摩擦帯電では、可視像を形成するに充分
な帯電量が得られていない。As is clear from FIG. 3, in the two-component developer, a sufficient amount of charge to form a visible image cannot be obtained by frictional charging between the developer and the developer carrier.
上記の如く、これまでに現像剤と現像担持体による摩擦
帯電によシ、可視像を形成するに充分な帯電量を有した
現像剤は開発されていない。As mentioned above, to date, no developer has been developed that has a sufficient amount of charge to form a visible image due to frictional charging between the developer and the developer carrier.
第2の問題点は現像ロール表面に極めて薄く平均に現像
剤を塗布する問題である。The second problem is that the developer is applied extremely thinly and evenly to the surface of the developing roll.
すなわち、第1図に図示しである現像ロール1に対し、
弾性グレードが1OOIZσ〜z500F/mの圧力で
圧接しておシ、現像剤容器中に存在している現像剤は、
現像ロールの回転により搬送され、弾性ブレードによシ
現像ロール表面に極めて薄く平均に塗布される。この為
、現像剤には、流動性、耐凝集性が良いことが要求され
る。That is, for the developing roll 1 shown in FIG.
When the elastic grade is pressed at a pressure of 1OOIZσ to z500F/m, the developer present in the developer container is
It is conveyed by the rotation of the developing roll, and is applied very thinly and evenly onto the surface of the developing roll by an elastic blade. For this reason, the developer is required to have good fluidity and agglomeration resistance.
しかるに、現像剤容器中に存在している現像剤は現像ロ
ールの回転によ)搬送されるが、応々にして、凝集性を
帯び塊状になる為、現像ロール表面に現像剤は塗布され
ない問題がある。However, although the developer present in the developer container is transported by the rotation of the developing roll, it sometimes becomes cohesive and becomes lumpy, resulting in the problem that the developer is not coated on the surface of the developing roll. There is.
又、現像ロールの回転によシ搬送されてきた現像剤は、
弾性グレードと現像ロール+i1ノの圧接力化において
急激に高い圧力を受けることになり、摩擦熱により現像
ロール表面に現像剤が軟化し固着する、固着現像剤の存
在は、現像ロール表面に極めて薄く平均に現像剤を塗布
することを防たける問題がある。これらの原因として、
現像剤の結着樹脂の軟化点が低いこと、ガラス転移点が
低いことが挙げられる。In addition, the developer transported by the rotation of the developing roll is
When the elastic grade and the developing roll + i1 are brought into contact, the pressure is suddenly high, and the developer softens and sticks to the developing roll surface due to frictional heat. There is a problem in preventing the application of developer evenly. These causes include
The binder resin of the developer has a low softening point and a low glass transition point.
更に、軟化点が高く、なると定)H温度力禄6くなシ、
通常の事務複写機に用いるには支障をきたす問題がある
。Furthermore, if the softening point is high,
There are problems that hinder its use in ordinary office copying machines.
本発明は上述の問題点に鑑みてなされたもので現像剤の
摩擦帯電量を制御することで、現像ロール表面に極めて
薄く均一に塗布でき、しかも流動性、耐凝集性に優れた
解像度の高いシャープな可視化像を形成し得る現像剤を
提供することを目的とする。The present invention has been made in view of the above-mentioned problems, and by controlling the amount of triboelectric charge of the developer, it is possible to coat the developing agent extremely thinly and uniformly on the surface of the developing roll, and to achieve high resolution with excellent fluidity and agglomeration resistance. An object of the present invention is to provide a developer capable of forming sharp visualized images.
本発明は結着樹脂に、着色剤を分散せしめてなる着色粒
子において、結着樹脂及び着色剤それぞれの帯電量を制
御することによシ、上記着色粒子の帯電量を制御し、現
像ロール表面に上記着色粒子を極めて薄く均一に塗布し
、解像度の高い、シャープな画像が得られる効果を有す
る現像剤を得ることを骨子とする。In the colored particles formed by dispersing a coloring agent in a binder resin, the present invention controls the amount of charge of the colored particles by controlling the amount of charge of each of the binder resin and the colorant. The main idea is to apply the above-mentioned colored particles extremely thinly and uniformly to obtain a developer that has the effect of producing sharp images with high resolution.
すなわち、本発明は、
表面に一成分現像剤を担持して回転し、該現像剤を静電
潜像に供給することによって潜像の現像を行なう現像ロ
ールと、該現gi!ロールの表面に前記現像剤を均一に
塗布する為に該現像ロールの表面に圧接するように配設
された弾性ブレードで基本的に構成される現像装置を用
いて静を潜像を非接触で現像する方法において、現像ロ
ールに塗布される現像剤の主成分である結着樹脂のガラ
ス転移点が50℃以上、軟化点が110℃〜160℃、
酸価が10〜40 であることを特徴とする現像剤でる
力、特にビスフェノール型ポリニスデル樹脂及びスチレ
ン−アクリル樹脂であることが望ましい。That is, the present invention provides a developing roll that rotates while carrying a one-component developer on its surface and develops a latent image by supplying the developer to the electrostatic latent image, and the developer gi! In order to uniformly apply the developer onto the surface of the roll, a developing device basically consisting of an elastic blade placed in pressure contact with the surface of the developing roll is used to generate a static latent image in a non-contact manner. In the developing method, the binder resin, which is the main component of the developer applied to the developing roll, has a glass transition point of 50°C or higher, a softening point of 110°C to 160°C,
It is desirable to use a developer characterized by an acid value of 10 to 40, particularly bisphenol type polynisder resin and styrene-acrylic resin.
上記着色剤としては一般に染料、顔料、カーボンブラッ
クなどでこのような着色剤としては、例えば、ニクロシ
ン染料、カーマイン染料、各−の塩基性染料、酸性染料
、油性染料、アントラキノン染料のような栄料5ベンジ
ジン系黄色有機顔料。The above-mentioned coloring agents are generally dyes, pigments, carbon black, etc., and examples of such coloring agents include nutrients such as nicrosine dyes, carmine dyes, basic dyes, acid dyes, oil dyes, and anthraquinone dyes. 5 Benzidine-based yellow organic pigment.
ギナントリン系有機顔料、ローダミン系有機顔料。Gynanthrin-based organic pigments, rhodamine-based organic pigments.
ンタロシアニン系有機顔料、酸化亜鉛、酸化チタン、ベ
ンガラなどの無機顔料のような顔料多ファーネスプラッ
ク、アセチレンジ2ツク、サーマルブラックなどのカー
ボンブランクをあげることができる。Pigment-rich furnace plaques such as inorganic pigments such as tantalocyanine-based organic pigments, zinc oxide, titanium oxide, and red iron oxide, acetylene dicarbonate, thermal black, and other carbon blanks can be mentioned.
次に、本発明の現像剤をうるための製造方法を一例を示
して以下に説明する。Next, a manufacturing method for obtaining the developer of the present invention will be explained below by showing an example.
まず、結着樹脂と着色剤をボールミル、V型混合機、S
型混合機、クーニングプレンダーなどの混合機で混合し
、得られた混合物を双Mニーダー9三本ロール、コニ−
グー、加圧ニーダ−9々どで混練し、この混線物をハン
マーミル、ジェットミル、ボールミルなどの粉砕機で粉
砕し、更に得ら等
れた粉体を篩、風力分級へで分級して所定粒径の粒子(
着色粒子)を造る。First, binder resin and colorant are mixed in a ball mill, V-type mixer,
The mixture is mixed using a mixer such as a mold mixer or a Kooning blender.
The mixture is kneaded using a pressure kneader, etc., and the mixture is crushed using a crusher such as a hammer mill, jet mill, or ball mill, and the resulting powder is further classified using a sieve or air classification. Particles of a predetermined particle size (
colored particles).
こうした着色粒子の製造にちた9、使用すべき結着樹脂
の種類及び分散すべき着色剤の種類、配合割合によシ得
られる着色粒子の帯電量の高低に影響を与える為、適宜
な帯電量のものが選択される。In the production of these colored particles9, the type of binder resin to be used, the type of colorant to be dispersed, and the blending ratio will affect the amount of charge of the colored particles obtained, so appropriate charging should be carried out. amount is selected.
上述した結着樹脂及び着色剤から選択された材料から得
られる着色粒子の帯電量はプラス帯電感光ドラムを使用
する場合マイナス0.5〜15μC/りであることが望
ましい。When a positively charged photosensitive drum is used, the amount of charge of the colored particles obtained from the materials selected from the above-mentioned binder resin and colorant is preferably -0.5 to 15 μC/liter.
又、必要に応じて、現像剤の流動性、耐凝集性を向上さ
せる為、着色粒子と同極性の疎水化されたコロイド状微
粒子を0.05〜2重量部、着色粒子の帯電量に影響を
与えない程度添加しても一向に差゛〜しつかえない。In addition, if necessary, in order to improve the fluidity and agglomeration resistance of the developer, 0.05 to 2 parts by weight of hydrophobized colloidal fine particles having the same polarity as the colored particles may be added, which will affect the amount of charge on the colored particles. Even if it is added to the extent that it does not cause any damage, there is no problem at all.
本発明に係る現像剤は、以下に列挙する種々の効果を奏
する。The developer according to the present invention has various effects listed below.
(1)現像ロール表面に極めて薄く均一に塗布できる現
像剤が得られる。(1) A developer can be obtained that can be applied extremely thinly and uniformly to the surface of the developing roll.
(11)効率の良いノφ擦帯電が得られる現像剤が得ら
れる。(11) A developer can be obtained that provides efficient triboelectric charging.
(lit)流動性の良い、1lllt凝集性のあるUM
像剤が得られる。(lit) UM with good fluidity and cohesiveness
An image agent is obtained.
(1v)解像度の高い、シャープな画像が得られる。(1v) Sharp images with high resolution can be obtained.
以下本発明を実施例を参照しながら説明する。 The present invention will be described below with reference to Examples.
実施例1
スチレy−アクリル樹脂(Mn 1 f3.300.1
14W328.000軟化点125℃、ガラス転移点6
1.2°G、酸価145)92重量部とカーボンブラッ
ク8重量部とせボールミルで約2時間混合した後、加圧
型ニーダ−で約1時間混練した。Example 1 Styrene y-acrylic resin (Mn 1 f3.300.1
14W328.000 Softening point 125℃, Glass transition point 6
1.2°G, acid value 145) and 8 parts by weight of carbon black were mixed in a ball mill for about 2 hours, and then kneaded in a pressure kneader for about 1 hour.
混線物を冷却後、ハンマーミルで粗粉砕後、ジェットミ
ルで微粉砕し、分級機で分級し、5〜25z+mの沿色
粒子とした。次いで前記着色粒子100重量部とコロイ
ド状微粒子(アエロジル几9722日本アエロジル社製
)0.5重量部とをボールミルにて混合し、該コロイド
状微粒子を該着色粒子の界面に付着せしめ50俤重量平
均粒径11.5−1の現像剤とした。After cooling the mixed material, it was coarsely pulverized with a hammer mill, finely pulverized with a jet mill, and classified with a classifier to obtain color-matching particles of 5 to 25z+m. Next, 100 parts by weight of the colored particles and 0.5 parts by weight of colloidal fine particles (Aerosil 9722 manufactured by Nippon Aerosil Co., Ltd.) were mixed in a ball mill, and the colloidal fine particles were adhered to the interface of the colored particles to give a weight average of 50 kg. The developer had a particle size of 11.5-1.
この現像剤の帯電量を測定した所マイナス6BpC/f
であった。The amount of charge of this developer was measured and found to be -6 BpC/f.
Met.
この現像剤を用い、第1図図示の現像装置において、・
感光体ドラムの表面電位グラス900v、′gL像バイ
アスマイナス500Vの条件で可視化像を形成せしめた
ところ、画像濃度15.解像力5Lp/wxで地かぶシ
の全くない良好な画像が得られた。又ヒートロール定着
器で定着した所140℃から定着が開始し、210℃で
もオフセットが生じなかった。Using this developer, in the developing device shown in FIG.
When a visualized image was formed under the conditions of a photoreceptor drum surface potential glass of 900V and a 'gL image bias of minus 500V, the image density was 15. A good image with no ground cover was obtained with a resolution of 5 Lp/wx. Furthermore, when fixing was performed using a heat roll fixing device, fixing started at 140°C, and no offset occurred even at 210°C.
実施例2
ビスフェノール型ポリエステル[脂(Mn4,100゜
MW32.000.軟化点135℃、ガラス転移点78
.5℃。Example 2 Bisphenol type polyester [fat (Mn 4, 100°MW 32.000. Softening point 135°C, glass transition point 78
.. 5℃.
酸価20.2)92重量部とカーボンブラック8重量部
と2時間ボールミルで分散後、実施例1と同様にして着
色粒子を得た。After dispersing 92 parts by weight of acid value 20.2 and 8 parts by weight of carbon black in a ball mill for 2 hours, colored particles were obtained in the same manner as in Example 1.
前記着色粒子100重量部とコロイド微粒子1重量部を
実施例1と同様にして該着色粒子の表面に付着せしめ5
0%重負平均粒径13.1μmの現像剤とした。100 parts by weight of the colored particles and 1 part by weight of the colloid fine particles were attached to the surface of the colored particles in the same manner as in Example 1.
A developer having a 0% weighted average particle size of 13.1 μm was used.
上記現像剤の帯電量はマイナス9.5/、lC/fであ
った実施例1と同様な条件で可視化像を形成せしめたと
ころ画像濃度1.51 、解像力5.6tp/IMの地
かぶりのない良好な画像が得られた。When a visualized image was formed under the same conditions as in Example 1, in which the charge amount of the developer was -9.5/lC/f, the image density was 1.51, and the resolution was 5.6 tp/IM. No good images were obtained.
又、150℃から定着が開始し、140”0〜220℃
でオフセットが生じなかった。Also, fixing starts from 150℃, and 140" from 0 to 220℃
No offset occurred.
実施例3
ビスフェノール型ポリエステル樹脂(軟化点(R&B法
)135℃、ガラス転移点81.2℃、酸価35)92
重量部とカーボンブラック8重力を部とを分散混合後、
実施例1と同様にして着色粒子を得、着色粒子100重
量部とコロイド状微粒子0.8重量部を実施例1と同様
にして現像剤とした。この現像剤の50%重量平均粒径
は、11,8μmで帯電量はマイナス13.6μC/f
実施例1と同様にして可視像を形成したところ画像濃度
1.4.解像力5 L 97mの地かぶシのない良好な
画像が得られ、定着も160℃から開始し140℃〜2
20℃でオフセットが生じたかった。Example 3 Bisphenol type polyester resin (softening point (R&B method) 135°C, glass transition point 81.2°C, acid value 35) 92
After dispersing and mixing parts by weight and 8 parts by gravity of carbon black,
Colored particles were obtained in the same manner as in Example 1, and 100 parts by weight of colored particles and 0.8 parts by weight of colloidal fine particles were used in the same manner as in Example 1 to prepare a developer. The 50% weight average particle diameter of this developer was 11.8 μm, and the charge amount was -13.6 μC/f.A visible image was formed in the same manner as in Example 1, and the image density was 1.4. A good image with a resolution of 5 L and 97 m without background fog was obtained, and fixing started from 160°C and from 140°C to 2
I wanted an offset to occur at 20°C.
比較例1〜3
軟化点、ガラス転移点、酸価の異なる結着樹脂を用い、
実施例1と同様に結着樹脂92重量部。Comparative Examples 1 to 3 Using binder resins with different softening points, glass transition points, and acid values,
Similar to Example 1, 92 parts by weight of binder resin.
カーボンブラック8重量部とを分散混合後、現像剤を得
た。After dispersing and mixing 8 parts by weight of carbon black, a developer was obtained.
実施例1と同様に特性を調べ表に示す結果を得た。The characteristics were investigated in the same manner as in Example 1, and the results shown in the table were obtained.
灰稙日Gray day
【図面の簡単な説明】
第1図は本発明に使用した現像装置の一例を示す概略図
、第2図は結着樹脂の酸価と現像剤のプローオフ法によ
る帯電量との関係を示す特性図、第3図は現像剤のブロ
ーオフ法による帯電量と第1図に示す現像法で得られた
帯電量との関係を示す特性図である。
1 現像ロール 20弾性ブレード3 現像剤容
器 4 現 像 剤5、 感光体ドラム 6
. 剛性金層片7 側 壁
代理人 弁理士 則 近 愚 佑
(ほか1名)
第 1 図
、マ
第 2 図
曲笑 イ西[Brief Description of the Drawings] Fig. 1 is a schematic diagram showing an example of the developing device used in the present invention, and Fig. 2 is a characteristic showing the relationship between the acid value of the binder resin and the amount of charge determined by the developer pull-off method. 3 are characteristic diagrams showing the relationship between the amount of charge obtained by the developer blow-off method and the amount of charge obtained by the development method shown in FIG. 1. 1 Developing roll 20 Elastic blade 3 Developer container 4 Developer 5, Photoreceptor drum 6
.. Rigid Gold Layer Piece 7 Side Wall Agent Patent Attorney Nori Chika Gusuke (and 1 other person) Figure 1, Figure 2 Figure 2 Laughter I Nishi
Claims (4)
を静電潜像に供給することによって潜像の現像を行なう
現像ロールと、該現像ロールの表面に前記現像剤を均一
に塗布する為に該現像ロールの表面に圧接するように配
設された弾性ブレードで基本的に構成される現像装置を
用いて静電潜像を非接触で現像する方法において用いる
現像剤において現像ロールに塗布される現像剤の主成分
である結着樹脂のガラス転移点が50℃以上、軟化点が
110℃〜160℃、酸価が10〜40であることを特
徴とする現像剤(1) A developing roll that carries a one-component developer on its surface and rotates to develop the latent image by supplying the developer to the electrostatic latent image, and the developer is uniformly distributed on the surface of the developing roll. A developing agent used in a method for non-contact developing an electrostatic latent image using a developing device basically consisting of an elastic blade disposed so as to come into pressure contact with the surface of the developing roll. A developer characterized in that the binder resin, which is the main component of the developer applied to the roll, has a glass transition point of 50°C or higher, a softening point of 110°C to 160°C, and an acid value of 10 to 40.
量部添加することを特徴とする特許請求の範囲第1項記
載の現像剤(2) The developer according to claim 1, wherein 0.05 to 2 parts by weight of colloidal silica is added to the developer.
ある特許請求の範囲第1項記載の現像剤(3) The developer according to claim 1, wherein the binder resin is a biphenyl type polyester resin.
許請求の範囲第1項記載の現像剤(4) The developer according to claim 1, wherein the binder resin is a styrene/acrylic resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59125305A JPH0642081B2 (en) | 1984-06-20 | 1984-06-20 | Developer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59125305A JPH0642081B2 (en) | 1984-06-20 | 1984-06-20 | Developer |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7167846A Division JP2930183B2 (en) | 1995-06-12 | 1995-06-12 | Developing device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS616656A true JPS616656A (en) | 1986-01-13 |
| JPH0642081B2 JPH0642081B2 (en) | 1994-06-01 |
Family
ID=14906799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59125305A Expired - Lifetime JPH0642081B2 (en) | 1984-06-20 | 1984-06-20 | Developer |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0642081B2 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63127254A (en) * | 1986-11-17 | 1988-05-31 | Ricoh Co Ltd | Toner for developing electrostatic latent image |
| JPH01259370A (en) * | 1988-04-11 | 1989-10-17 | Mitsubishi Rayon Co Ltd | Binder resin and toner for toner |
| JPH0264558A (en) * | 1988-08-31 | 1990-03-05 | Canon Inc | Negatively chargeable toner composition |
| JPH07319211A (en) * | 1995-06-12 | 1995-12-08 | Toshiba Corp | One-component non-magnetic developer |
| US10099028B2 (en) | 2010-08-16 | 2018-10-16 | Breathe Technologies, Inc. | Methods, systems and devices using LOX to provide ventilatory support |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS49104639A (en) * | 1973-01-09 | 1974-10-03 | ||
| JPS5315655A (en) * | 1976-07-28 | 1978-02-13 | Sanyo Electric Co Ltd | Absorption hot and cold water supplying device |
| JPS55144255A (en) * | 1979-04-28 | 1980-11-11 | Canon Inc | Developing method and its apparatus |
| JPS56116041A (en) * | 1980-02-18 | 1981-09-11 | Toyobo Co Ltd | Binder for photographic toner |
| JPS58113944A (en) * | 1981-12-26 | 1983-07-07 | Kinoshita Kenkyusho:Kk | Production of electrostatic latent image developer |
| JPS597960A (en) * | 1982-07-06 | 1984-01-17 | Canon Inc | Heat fixable dry type toner |
-
1984
- 1984-06-20 JP JP59125305A patent/JPH0642081B2/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS49104639A (en) * | 1973-01-09 | 1974-10-03 | ||
| JPS5315655A (en) * | 1976-07-28 | 1978-02-13 | Sanyo Electric Co Ltd | Absorption hot and cold water supplying device |
| JPS55144255A (en) * | 1979-04-28 | 1980-11-11 | Canon Inc | Developing method and its apparatus |
| JPS56116041A (en) * | 1980-02-18 | 1981-09-11 | Toyobo Co Ltd | Binder for photographic toner |
| JPS58113944A (en) * | 1981-12-26 | 1983-07-07 | Kinoshita Kenkyusho:Kk | Production of electrostatic latent image developer |
| JPS597960A (en) * | 1982-07-06 | 1984-01-17 | Canon Inc | Heat fixable dry type toner |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63127254A (en) * | 1986-11-17 | 1988-05-31 | Ricoh Co Ltd | Toner for developing electrostatic latent image |
| JPH01259370A (en) * | 1988-04-11 | 1989-10-17 | Mitsubishi Rayon Co Ltd | Binder resin and toner for toner |
| JPH0264558A (en) * | 1988-08-31 | 1990-03-05 | Canon Inc | Negatively chargeable toner composition |
| JPH07319211A (en) * | 1995-06-12 | 1995-12-08 | Toshiba Corp | One-component non-magnetic developer |
| US10099028B2 (en) | 2010-08-16 | 2018-10-16 | Breathe Technologies, Inc. | Methods, systems and devices using LOX to provide ventilatory support |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0642081B2 (en) | 1994-06-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |