JPS6211864A - Electrophotographic developer - Google Patents
Electrophotographic developerInfo
- Publication number
- JPS6211864A JPS6211864A JP60150125A JP15012585A JPS6211864A JP S6211864 A JPS6211864 A JP S6211864A JP 60150125 A JP60150125 A JP 60150125A JP 15012585 A JP15012585 A JP 15012585A JP S6211864 A JPS6211864 A JP S6211864A
- Authority
- JP
- Japan
- Prior art keywords
- toner
- carrier
- developer
- resin
- weight
- 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
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
- G03G9/0802—Preparation methods
- G03G9/081—Preparation methods by mixing the toner components in a liquefied state; melt kneading; reactive mixing
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Developing Agents For Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は電子写真の静電潜像の現像に用いられる電子写
真用現像剤に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to an electrophotographic developer used for developing electrostatic latent images in electrophotography.
〈従来の技術〉
一般に電子写真法および静電記録法においては、像支持
体−Fに形成された静電潜像を現像するために、トナー
とキャリヤーよりなる現像剤が用いられる。<Prior Art> Generally, in electrophotography and electrostatic recording, a developer consisting of a toner and a carrier is used to develop an electrostatic latent image formed on an image support -F.
この現像剤を構成するトナーは、搬送の過程でキャリヤ
ーと相互に摩擦されて静電潜像とは反対極性の電荷がト
ナーに誘起され、現像器による現像の過程で該トナーが
像支持体に静電的に付着して可視像が形成される。負極
性の潜像を現像する際は、正極性の電荷制御剤が配合さ
れたトナーがキャリヤーと摩擦することにより正電荷を
保持し負極性の潜像を現像ならしめ、一方、正極性の潜
像を現像する際は、負極性の電荷制御剤が配合されたト
ナーが現像に供される。The toner constituting this developer is rubbed against the carrier during the transportation process, and a charge of the opposite polarity to that of the electrostatic latent image is induced in the toner, and during the process of development by the developer, the toner is transferred to the image support. Electrostatic deposition forms a visible image. When developing a negative latent image, a toner containing a positive charge control agent retains a positive charge by friction with the carrier and develops a negative latent image; When developing an image, a toner containing a negative charge control agent is used for development.
しかるに従来の現像剤においては摩擦帯電性が不安定で
あり、と(に連続コピーに際してキャリヤー表面へのト
ナーのスペント現象にともなう帯電量の低下を生じ画像
においてカブリが発生するという欠点があった。この場
合の帯電量の低下は連続コピーの比較的初期に顕著に現
れ、その後は比較的縁やかな低下現象を示す。例えば初
期の帯電量が15uc/gの場合、数100枚のコピー
で10uc/g程度に低下し、その後はIt較的安定し
ながら徐々に低下する。However, conventional developers have unstable triboelectric charging properties, and have the disadvantage that during continuous copying, the amount of charge decreases due to the phenomenon of toner spent on the carrier surface, resulting in fogging of images. In this case, the decrease in the charge amount becomes noticeable at a relatively early stage of continuous copying, and thereafter shows a relatively gradual decrease.For example, if the initial charge amount is 15 uc/g, after several hundred copies, 10 uc/g decreases. /g, and then gradually decreases while remaining relatively stable.
このような帯電量1f4の劣化対策として、初期の帯電
量あらかじめ高く設定することが考えられる。As a countermeasure against such deterioration of the charge amount 1f4, it is conceivable to set the initial charge amount high in advance.
しかしこの場合は数100枚のコピー後は連続コピーの
安定化領域に入るものの、初期においては帯電量が高す
ぎて画像濃度不良を生ずる。この初期の画像濃度不足を
解消するために例えば (1)トナーとキャリヤーの混
合時間を長(する、(2)流動調整剤等添加剤をトナー
にまぶし帯電量をコン[・ロールする、ことが考えられ
る。しかし、この場合も前者は現像剤作製時の作業性が
悪く、又、長時間の混合によりトナーの一部が破壊され
る問題を有し、一方後者は現像剤の製造工程が増えコス
ト高になり、又、添加剤自体力月・リーー、キャリヤー
間の摩擦帯電性に微妙な影響を及ぼし初期の帯電量のコ
ントロールは出来てもかならずしも長時間の連続コピー
において安定した摩擦帯電性を得るものではない。However, in this case, although it enters the stable region of continuous copying after several hundred copies have been made, the amount of charge is too high in the initial stage, resulting in poor image density. In order to eliminate this initial image density deficiency, it is possible to (1) lengthen the mixing time of the toner and carrier, (2) to control the amount of charge by coating the toner with additives such as flow control agents. However, in this case as well, the former has problems with poor workability during developer preparation and part of the toner is destroyed due to long-term mixing, while the latter requires an additional developer manufacturing process. The cost is high, and the additive itself has a subtle effect on the triboelectricity between the carriers, so even if it is possible to control the amount of initial charge, it is not always possible to maintain stable triboelectricity during long-term continuous copying. It's not something you get.
又、トナーに各種の電荷制御剤を配合したり、あるいは
特開昭53−100242や特開昭59−9670のご
とくキャリヤーのコーティング剤にトナーと逆極性の電
荷制御剤を配合することも試みられているが、」一連の
ごとき問題を根本的に解決するには至っていない。Additionally, attempts have been made to blend various charge control agents into the toner, or to blend a charge control agent with the opposite polarity to the toner into the carrier coating agent as in JP-A-53-100242 and JP-A-59-9670. However, these problems have not been fundamentally solved.
〈発明が解決しようとする問題点〉
本発明は電子写真の静電潜像の現像に用いる二成分現像
剤に生しやすい連続コピ一時の安定性、すなわちコピー
の初期と連続コピ一時との間でトナーの摩擦帯電量の変
動が少ない現像剤を得ようとするものであり、これによ
り現像の初期から常に良好な画質のコピーを得ようとす
るものである。<Problems to be Solved by the Invention> The present invention solves the problem of stability during continuous copying, which tends to occur in two-component developers used for developing electrostatic latent images in electrophotography, that is, between the initial stage of copying and the first stage of continuous copying. The objective is to obtain a developer with little variation in the amount of triboelectric charge of the toner, and thereby to obtain copies of good image quality at all times from the initial stage of development.
く問題点を解決するための手段〉
本発明の特徴とするところは、上記の問題を解決するた
めにコーティングキャリヤーの塗被層にトナーに配合さ
れている電荷制御剤と同極性の電荷制御剤を配合したこ
とにあり、更にはトナーの摩擦帯電量の絶対値が10〜
2Q1+c/gになるようトナーおよびコーティングキ
ャリヤーの組成により制御されていることである。Means for Solving the Problems> The present invention is characterized in that, in order to solve the above problems, a charge control agent having the same polarity as the charge control agent contained in the toner is added to the coating layer of the coating carrier. Furthermore, the absolute value of the triboelectric charge amount of the toner is 10~10.
It is controlled by the composition of toner and coating carrier so that it becomes 2Q1+c/g.
3一
本発明でいうキャリヤーは次のような構成を有する。す
なわち10〜500j+mの鉄粉、酸化処理鉄粉、ニッ
ケル、コバルト、鉄/ケイ素/アルミニウム合金、フェ
ライト粒子等からなる帯磁性粒子の表面に電荷制御剤と
結着剤樹脂からなる被覆層を設けてなるコーティングキ
ャリヤーが適用される。31 The carrier referred to in the present invention has the following configuration. That is, a coating layer made of a charge control agent and a binder resin is provided on the surface of magnetic particles made of 10 to 500 J+m of iron powder, oxidized iron powder, nickel, cobalt, iron/silicon/aluminum alloy, ferrite particles, etc. A coating carrier is applied.
該電荷制御剤はトナーに正帯電性電荷制御剤を使用する
場合は正帯電性電荷制御剤、すなわち二一グロシン、炭
素数2〜]6のアルキル基を含むアジン系染料、C,1
,Ba5ic Violet 1 、C,I。When a positively chargeable charge control agent is used in the toner, the charge control agent is a positively chargeable charge control agent, i.e., 21 glosine, an azine dye containing an alkyl group having 2 to 6 carbon atoms, C,1
, Ba5ic Violet 1, C,I.
Ba5ic Violet 3、C,T、 l1asi
c l1lue 1 、C。Ba5ic Violet 3, C, T, l1asi
c l1lue 1, C.
1、Ba5ic l1lue 3、等の塩基性染f1、
該塩基性染料のし一−F顔料、四級アンモニウム地、ア
ルコキシル化アミン等が適用され、一方、トナーに負帯
電性電荷制御剤を使用する場合は負帯電性電荷制御剤、
ずなわちアゾ系の含金染料、非染料系の金属錯体、塩素
化パラフィン、塩素化ポリエステル等が適用される。1, basic dye f1 such as Ba5ic l1lue 3,
The basic dye Shii-F pigment, quaternary ammonium base, alkoxylated amine, etc. are applied, while when a negatively chargeable charge control agent is used in the toner, a negatively chargeable charge control agent,
Specifically, azo-based metal-containing dyes, non-dye-based metal complexes, chlorinated paraffins, chlorinated polyesters, etc. are applicable.
これらの電荷制御剤を帯磁性粒子の表面に固着させるた
めの結着剤樹脂としては例えばアクリル酸エステルとス
チレンの共重合体、スチレンとブタジェンの共重合体、
ポリ塩化ビニル、エポキシ樹脂、ポリビニルブチラール
、ポリウレタン等通常コーティングキャリヤー用に使用
されている樹脂が本発明に使用される。Examples of the binder resin for fixing these charge control agents to the surface of the magnetic particles include a copolymer of acrylic acid ester and styrene, a copolymer of styrene and butadiene,
Resins commonly used for coating carriers, such as polyvinyl chloride, epoxy resins, polyvinyl butyral, polyurethane, etc., can be used in the present invention.
上記の材料を使って本発明でいうキャリヤーを製造する
には結着剤樹脂溶液中に電荷制御剤および帯磁性粒子を
分散させ、流動化ベッド法、スプレードライ法などを使
用して溶剤を除去し帯磁性粒子表面に塗被層を設ける。To manufacture the carrier referred to in the present invention using the above materials, a charge control agent and magnetic particles are dispersed in a binder resin solution, and the solvent is removed using a fluidized bed method, spray drying method, etc. A coating layer is provided on the surface of the magnetic particles.
この際使用する溶剤はトリクロルエチレン、トルエン、
メチルエチルケトン、キシレン、シクロヘキサノン、ア
セトン等広範囲のものが使用できる。又、本発明でいう
キャリヤーの塗被層には、例えば樹脂酸変性アジン化合
物のごとき予め電荷制御剤に樹脂分が配合されている場
合は敢て結着剤樹脂を配合する必要はない。樹脂酸変性
のアジン化合物としては例えばオリエント化学社から上
市されているボントロンN−04がある。The solvents used at this time are trichlorethylene, toluene,
A wide range of substances can be used, such as methyl ethyl ketone, xylene, cyclohexanone, and acetone. Further, in the coating layer of the carrier referred to in the present invention, there is no need to intentionally incorporate a binder resin in the case where a resin component, such as a resin-acid-modified azine compound, is previously blended with a charge control agent. An example of a resin acid-modified azine compound is Bontron N-04, which is marketed by Orient Chemical Co., Ltd.
なお、本発明でいうキャリヤー被覆剤には必要に応じて
着色顔料や可塑剤等の添和物を適宜選択して含有さゼる
ことかできる。又、本発明でいう被覆キャリヤーは通常
の二成分系現像剤に使用される酸化鉄粉の表面に前述の
方法にて被覆処理したもののほかに、電荷制御剤が内添
されている結着剤中にマグネタイト等の超微粒子状の帯
磁性物質を練り込んだものを所望の大きさに粉砕したも
のでもよい。The carrier coating material used in the present invention may contain additives such as coloring pigments and plasticizers, if necessary. In addition to the coated carrier used in the present invention, which is coated on the surface of iron oxide powder used in ordinary two-component developers by the above-mentioned method, the coated carrier may also include a binder to which a charge control agent is internally added. It may also be one in which ultrafine particulate magnetic substances such as magnetite are kneaded and then pulverized to a desired size.
上記の構成からなるキャリヤーと併用するトナーは次の
構成を有する。すなわち、アクリル系樹脂、ポリエステ
ル樹脂、エポキシ樹脂等の結着剤樹脂、カーボンブラッ
ク等の着色剤および電荷制御剤を熱溶融混練し、10〜
201unの粒子径になるよう粉砕分級して本発明のト
ナーを得ることができる。この場合のトナーに配合する
電荷制御剤はキャリヤーの塗被層に配合されるものと同
極性であることが要求されるが組成はかならずしも同一
でなくてもよい。The toner used in combination with the carrier having the above structure has the following structure. That is, a binder resin such as an acrylic resin, a polyester resin, or an epoxy resin, a coloring agent such as carbon black, and a charge control agent are hot-melted and kneaded.
The toner of the present invention can be obtained by crushing and classifying the particles to have a particle size of 201 nm. In this case, the charge control agent blended into the toner is required to have the same polarity as that blended into the coating layer of the carrier, but the composition does not necessarily have to be the same.
上記のキャリヤーとトナーからなる現像剤は、ブローオ
フ法によるトナーの摩擦帯電量の絶対値が10〜20u
c/gになるようキャリヤーおよびトナーの材料設計を
おこなう必要がある。つまり感光層の光導電体がセレン
の如きP型の場合は、トナーの帯電極性は負帯電に、一
方、光導電体が酸化亜鉛の如きN型の場合は、トナーの
帯電極性は正帯電になるよう電荷制御剤が選択される。The developer consisting of the above carrier and toner has an absolute value of triboelectric charge amount of the toner of 10 to 20u by the blow-off method.
It is necessary to design the materials of the carrier and toner so that the ratio of c/g is achieved. In other words, if the photoconductor in the photosensitive layer is P-type, such as selenium, the toner's charge polarity will be negatively charged, whereas if the photoconductor is N-type, such as zinc oxide, the toner's charge polarity will be positively charged. The charge control agent is selected so that
そしてトナーの摩擦帯電量を絶対値で10〜20uc/
gの範囲に制御するには、トナーおよびキャリヤーの塗
被層に配合する電荷制御剤の種類と配合量、コーティン
グキャリヤーの塗布量、併用する結着剤樹脂の種類を適
宜選択し組合わせることにより可能である。すなわちト
ナー中の電荷制御剤は結着剤樹脂100重量部に対し3
〜10重量部配合されるのに対して、キャリヤーの塗被
層中の電荷制御剤は結着剤樹脂100重量部に対し3〜
200重量部であって配合量に対する選択範囲がきわめ
て大きい。又、コーティングキャリヤーの塗布は0.5
〜10III111好ましくは5III11以下の薄膜
にコントロールされる。 このような構成からなる本発
明の現像剤はトナーおよびキャリヤー表面に同極性の電
荷制御剤が配合されながらも、両者の微妙な摩擦帯電系
列の相互作用により、静電潜像を現像するのに好適なト
ナーの摩擦帯電特性が維持され本発明をなしうるに至っ
た。Then, the amount of triboelectric charge of the toner is 10 to 20 uc/
g range, by appropriately selecting and combining the type and amount of charge control agent to be added to the coating layer of toner and carrier, the amount of coating carrier applied, and the type of binder resin used together. It is possible. That is, the charge control agent in the toner is 3 parts by weight per 100 parts by weight of the binder resin.
The amount of charge control agent in the carrier coating layer is 3 to 10 parts by weight per 100 parts by weight of the binder resin.
It is 200 parts by weight, so the selection range for the amount to be added is extremely wide. Also, the coating carrier is applied at a rate of 0.5
The thickness of the film is controlled to be 10III111, preferably 5III11 or less. Although the developer of the present invention having such a structure contains a charge control agent of the same polarity on the toner and carrier surfaces, it is difficult to develop an electrostatic latent image due to the delicate frictional charging series interaction between the two. The present invention was made possible by maintaining suitable triboelectric properties of the toner.
〈実施例〉
以下実施例および比較例により本発明をさらに詳述する
。<Examples> The present invention will be further explained in detail with reference to Examples and Comparative Examples below.
実施例1
スチレン/ブタジェン共重合体樹脂(プライオライド5
−5A、グツドイヤー社製)10重量部および正帯電性
電荷制御剤としてアジン化合物(ボントロンN−01、
オリエント化学社製)10重量部をトルエン500重量
部に溶解した溶液により、流動化ベッド装置を用いて、
酸化鉄粉(EFV200/300、日本鉄粉社製)1k
gに前記溶液をスプレーして80℃の温度で乾燥し、厚
さ1〜2μmの被覆層を有するギヤリヤーを得た。Example 1 Styrene/butadiene copolymer resin (Priolide 5
-5A, manufactured by Gutdeyer) and 10 parts by weight of an azine compound (Bontron N-01,
Using a fluidized bed apparatus, a solution of 10 parts by weight (manufactured by Orient Chemical Co., Ltd.) dissolved in 500 parts by weight of toluene,
Iron oxide powder (EFV200/300, manufactured by Nippon Iron Powder Co., Ltd.) 1k
The above solution was sprayed onto a glass plate and dried at a temperature of 80° C. to obtain a gear having a coating layer with a thickness of 1 to 2 μm.
一方、スチレン/アクリル酸エステル共重合体樹脂(プ
ライオライドAC,グツドイヤー社製)100重量部、
アジン化合物(ポントロンN−01、オリエント化学社
製)5重量部、カーボンブラック(三菱カーボンブラッ
ク#40、三菱化成社製)3重量部を熱溶融混練後、冷
却し、微粉砕して平均粒径12umの正帯電性トナーを
作製した。On the other hand, 100 parts by weight of styrene/acrylic ester copolymer resin (Prioride AC, manufactured by Gutdeyer),
5 parts by weight of an azine compound (Pontron N-01, manufactured by Orient Chemical Co., Ltd.) and 3 parts by weight of carbon black (Mitsubishi Carbon Black #40, manufactured by Mitsubishi Kasei Corporation) were hot-melted and kneaded, cooled, and finely pulverized to have an average particle size. A positively chargeable toner having a thickness of 12 um was prepared.
上記のキャリヤー100重量部とトナー5重量部を混合
して本発明の現像剤を作製し、ブローオフ帯電量測定装
置(東芝ケミカル社製)に適用し、トナーの摩擦帯電量
を測定したところ15uc/gであった。次にこの現像
剤を酸化亜鉛感光体を有するPPC複写機に適用し初期
画像を撮ったところ、マクベス反射濃度計による10m
mφペタの画像濃度は1.5であって十分な濃度を示し
、カブリの発生がない鮮明な画像を得た。さらにこのP
PC複写機を使って5000枚の連続コピーをおこなっ
たところ、画像濃度およびカブリは初期の状態をそのま
ま維持するものであり鮮明な画像を再現した。この場合
のトナーの摩擦帯電量は14.5uc/gであり初期の
帯電量とほとんど同等であり、高画質を裏付けるもので
あった。The developer of the present invention was prepared by mixing 100 parts by weight of the above carrier and 5 parts by weight of toner, and the developer was applied to a blow-off charge measuring device (manufactured by Toshiba Chemical Corporation) to measure the amount of triboelectric charge of the toner. It was g. Next, this developer was applied to a PPC copying machine with a zinc oxide photoreceptor and an initial image was taken.
The image density of mφ peta was 1.5, which was a sufficient density, and a clear image without fogging was obtained. Furthermore, this P
When 5,000 sheets were continuously copied using a PC copying machine, the image density and fog remained at their initial state, and clear images were reproduced. The triboelectric charge amount of the toner in this case was 14.5 uc/g, which was almost the same as the initial charge amount, which supported the high image quality.
実施例2
正帯電性電荷制御剤である樹脂酸変性アシン化合物(ボ
ントロンN−04、オリエント化学社製)15重量部を
メチルエチルケトン500重量部に溶解した溶液により
、流動化ヘット装置を用いて、酸化鉄粉(EFV200
/300、日本鉄粉11−製)1kgに前記溶液をスプ
レーして70℃の温度で乾燥し、厚さ1〜2tj■の被
覆層を’Mずろキャリヤーを得た。Example 2 A solution of 15 parts by weight of a resin acid-modified asine compound (Bontron N-04, manufactured by Orient Chemical Co., Ltd.), which is a positively chargeable charge control agent, dissolved in 500 parts by weight of methyl ethyl ketone was oxidized using a fluidization head device. Iron powder (EFV200
The above solution was sprayed onto 1 kg of Nippon Steel Powder 11-300 (manufactured by Japan Iron Powder 11-) and dried at a temperature of 70 DEG C. to obtain a coating layer having a thickness of 1 to 2 mm.
一方、スチレン/アクリル酸コ゛−ステル共重合体樹脂
(ブライオライドAC,グツドイヤーiL製)5重量部
、樹脂酸変性アシン化合物(ボントロンN−04、オリ
エント化学社製)5重量部、ツノ−ボンブラック(三菱
ツノ−ボンブラック#40、三菱化成社製)3重量部を
熱溶融混練後、冷却、微粉砕して平均粒径14.21℃
mの正帯電性トナーを作製した。On the other hand, 5 parts by weight of styrene/acrylic acid co-ester copolymer resin (Bryolide AC, manufactured by Gutdeyer iL), 5 parts by weight of resin acid-modified acine compound (Bontron N-04, manufactured by Orient Chemical Co., Ltd.), Tsunobon Black (manufactured by Orient Chemical Co., Ltd.) After hot-melting and kneading 3 parts by weight of Mitsubishi Tsunobon Black #40 (manufactured by Mitsubishi Kasei Corporation), it was cooled and pulverized to give an average particle size of 14.21°C.
A positively chargeable toner of m was prepared.
上記のキャリヤー100重量部とトナー5重量部を混合
して本発明の現像剤を作製し、ブローオフ法により測定
したところ17uc/gであった。A developer of the present invention was prepared by mixing 100 parts by weight of the above carrier and 5 parts by weight of toner, and the developer was measured by a blow-off method and found to be 17 uc/g.
この現像剤を酸化亜鉛感光体を有するPPC複写機に適
用し画像特性をみたところ、実施例1と同様のすぐれた
効果が確認された。なお、5000枚コピー後のトリー
−の帯電量は15uc/gであり、高画質を裏付けるも
のであった。When this developer was applied to a PPC copying machine having a zinc oxide photoreceptor and its image characteristics were examined, excellent effects similar to those of Example 1 were confirmed. The amount of charge on the tree after 5,000 copies was 15 uc/g, confirming the high image quality.
実施例3
スチレン/ブタジェン共重合体樹脂(プライオライl−
8−5A)10重量部および負帯電性電荷制御剤である
アゾ系金属錯塩染料(メタルブラックT−1−48、保
土谷化学工業社製)10重量部をトルエン500重量部
に溶解した溶液により、流動化ベッド装置を用いて、酸
化鉄粉(EFV200/300)1kgに前記溶液をス
プレーシて80℃の温度で乾燥し、厚さ1〜2μmの被
覆層を有するキャリヤーを得た。Example 3 Styrene/butadiene copolymer resin (Priory l-
8-5A) and 10 parts by weight of an azo metal complex dye (Metal Black T-1-48, manufactured by Hodogaya Chemical Industry Co., Ltd.), which is a negatively chargeable charge control agent, in 500 parts by weight of toluene. The above solution was sprayed onto 1 kg of iron oxide powder (EFV200/300) using a fluidized bed apparatus and dried at a temperature of 80°C to obtain a carrier having a coating layer with a thickness of 1 to 2 μm.
一方、スチレン/アクリル酸エステル共重合体樹脂(プ
ライオライドAC,グツドイヤー社製)100重量部、
アゾ系金属錯塩染料(メタルブラックT−4−48)3
重量部、ツノ−ボンブラック(三菱カーボンブラック#
40、三菱化成社製)= 11−
製)3重量部を熱溶融混練、冷却、微粉砕して平均粒径
151+mの負帯電性トナーを作製した。On the other hand, 100 parts by weight of styrene/acrylic ester copolymer resin (Prioride AC, manufactured by Gutdeyer),
Azo metal complex dye (Metal Black T-4-48) 3
Weight part, Horn Bon Black (Mitsubishi Carbon Black #
40 (manufactured by Mitsubishi Kasei Corporation) = 3 parts by weight (manufactured by Mitsubishi Kasei Corporation) = 11-) was hot-melted and kneaded, cooled, and pulverized to prepare a negatively chargeable toner having an average particle size of 151+m.
上記のキャリヤー100重量部とトナー6重量部を混合
して得られた本発明の現像剤をブローオフ測定装置にか
けてトナーの帯電量を測定したところ−17uc/ g
であった。The developer of the present invention obtained by mixing 100 parts by weight of the above carrier and 6 parts by weight of toner was applied to a blow-off measuring device to measure the charge amount of the toner, and it was -17 uc/g.
Met.
この現像剤Se感光体を有するPPC複写機に適用し画
像特性をみたところ、実施例1と同様のすぐれた効果が
確認された。なお、5000枚連続コピー後のトナーの
帯電量は一16uc/gであり、高画質画像を裏付ける
ものであった。When this developer was applied to a PPC copying machine having a Se photoreceptor and its image characteristics were observed, excellent effects similar to those of Example 1 were confirmed. Note that the amount of charge of the toner after 5000 sheets of continuous copying was -16 uc/g, which confirmed the high quality images.
比較例
スチレン/ブタジェン共重合体樹脂(プライオライドS
−5A)10重量部および負帯電性電荷制御剤であるア
ゾ系金属錯塩染料(T −4−−48)3重量部をトル
エン500重量部に溶解した溶液を用いて、上記各実施
例と同要領でコーティングキャリヤーを作製した。Comparative Example Styrene/butadiene copolymer resin (Priolide S
-5A) and 3 parts by weight of azo metal complex dye (T-4--48), which is a negatively chargeable charge control agent, were dissolved in 500 parts by weight of toluene in the same manner as in each of the above examples. A coated carrier was prepared according to the procedure.
一方、スチレン/アクリル酸エステル共重合体樹脂(プ
ライオライドAC)100重量部、アジン化合物(ボン
トロンN−01)5重量部、カーボンブラック(三菱カ
ーボンブラック#40)3重量部を熱溶融混練、微粉砕
して平均粒径12un+の正帯電性トナーを作製した。On the other hand, 100 parts by weight of a styrene/acrylic ester copolymer resin (Priolide AC), 5 parts by weight of an azine compound (Bontron N-01), and 3 parts by weight of carbon black (Mitsubishi Carbon Black #40) were hot-melted and kneaded. This was pulverized to produce a positively chargeable toner having an average particle size of 12un+.
上記のキャリヤー100重量部とトナー5重量部を混合
して比較用の現像剤を作製し、ブローオフ法によりトナ
ーの摩擦帯電量を測定したところ16.5すc/gであ
った。A comparative developer was prepared by mixing 100 parts by weight of the above carrier and 5 parts by weight of toner, and the amount of triboelectric charge of the toner was measured by a blow-off method and found to be 16.5 sc/g.
この現像剤を酸化亜鉛感光体を有するPPC複写機に適
用し画像特性をみたところ、初期においては画像濃度1
.5以上でカブリのない良好な画像が得られたが、10
00枚程度の連続コピーでカブリが発生し、該比較用現
像剤が実用上支障をきたすものであることが確認された
。なお、1000枚連続コピー後のトナーの帯電量は1
0μc/gであり、大幅な劣化が確認された。When this developer was applied to a PPC copying machine with a zinc oxide photoreceptor and the image characteristics were examined, it was found that the image density was 1 at the initial stage.
.. A good image without fogging was obtained with a value of 5 or more, but a value of 10
Fog occurred after continuous copying of approximately 00 sheets, and it was confirmed that the comparative developer caused problems in practical use. The amount of charge on the toner after 1000 sheets of continuous copying is 1.
It was 0 μc/g, and significant deterioration was confirmed.
〈発明の効果〉
以上の実施例からも明らかなように本発明によれば、連
続コピ一時における摩擦帯電特性の安定化が可能となり
、所期の目的を達成することができる。<Effects of the Invention> As is clear from the above embodiments, according to the present invention, it is possible to stabilize the triboelectric charging characteristics during continuous copying, and the intended purpose can be achieved.
Claims (1)
とキャリヤーとからなる現像剤において、該キャリヤー
が帯磁性粒子の表面にトナーに配合されている電荷制御
剤と同極性の電荷制御剤を含有した被膜を設けたことを
特徴とする電子写真用現像剤。 2 前記トナーの摩擦帯電量の絶対値が10〜20μc
/gに制御されてい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。[Scope of Claims] 1. A developer consisting of a toner and a carrier whose main components are a binder resin and a charge control agent, in which the carrier is formed on the surface of magnetic particles in the same manner as the charge control agent blended in the toner. An electrophotographic developer comprising a coating containing a polar charge control agent. 2 The absolute value of the triboelectric charge amount of the toner is 10 to 20 μc.
2. The electrophotographic developer according to claim 1, wherein the electrophotographic developer is controlled to have a content of /g.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60150125A JPS6211864A (en) | 1985-07-10 | 1985-07-10 | Electrophotographic developer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60150125A JPS6211864A (en) | 1985-07-10 | 1985-07-10 | Electrophotographic developer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6211864A true JPS6211864A (en) | 1987-01-20 |
Family
ID=15490025
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60150125A Pending JPS6211864A (en) | 1985-07-10 | 1985-07-10 | Electrophotographic developer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6211864A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008146527A1 (en) * | 2007-05-29 | 2008-12-04 | Sharp Kabushiki Kaisha | Developing agent, developing unit, developing device, and apparatus for image formation |
JP2008298891A (en) * | 2007-05-29 | 2008-12-11 | Sharp Corp | Carrier, developer, developing device, image forming apparatus and image forming method |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59157656A (en) * | 1983-02-28 | 1984-09-07 | Nippon Teppun Kk | Carrier material for electrostatic image development |
JPS60115947A (en) * | 1983-11-28 | 1985-06-22 | Olympus Optical Co Ltd | Carrier for electrophotographic developer |
-
1985
- 1985-07-10 JP JP60150125A patent/JPS6211864A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59157656A (en) * | 1983-02-28 | 1984-09-07 | Nippon Teppun Kk | Carrier material for electrostatic image development |
JPS60115947A (en) * | 1983-11-28 | 1985-06-22 | Olympus Optical Co Ltd | Carrier for electrophotographic developer |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008146527A1 (en) * | 2007-05-29 | 2008-12-04 | Sharp Kabushiki Kaisha | Developing agent, developing unit, developing device, and apparatus for image formation |
JP2008298891A (en) * | 2007-05-29 | 2008-12-11 | Sharp Corp | Carrier, developer, developing device, image forming apparatus and image forming method |
US8192908B2 (en) | 2007-05-29 | 2012-06-05 | Sharp Kabushiki Kaisha | Carrier, developer, development device, image forming apparatus and image forming method |
CN102681377A (en) * | 2007-05-29 | 2012-09-19 | 夏普株式会社 | Carrier, developer, development device, image forming apparatus and image forming method |
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