JPH03146959A - Dichroic electrophotographiing method - Google Patents

Dichroic electrophotographiing method

Info

Publication number
JPH03146959A
JPH03146959A JP1285023A JP28502389A JPH03146959A JP H03146959 A JPH03146959 A JP H03146959A JP 1285023 A JP1285023 A JP 1285023A JP 28502389 A JP28502389 A JP 28502389A JP H03146959 A JPH03146959 A JP H03146959A
Authority
JP
Japan
Prior art keywords
developer
toner image
development
color
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
Application number
JP1285023A
Other languages
Japanese (ja)
Inventor
Hidehiko Soyama
曽山 秀彦
Masanori Ichimura
市村 正則
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.)
Fujifilm Business Innovation Corp
Original Assignee
Fuji Xerox 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 Fuji Xerox Co Ltd filed Critical Fuji Xerox Co Ltd
Priority to JP1285023A priority Critical patent/JPH03146959A/en
Priority to GB9021918A priority patent/GB2238395B/en
Priority to KR1019900015992A priority patent/KR910010252A/en
Priority to DE4032702A priority patent/DE4032702A1/en
Publication of JPH03146959A publication Critical patent/JPH03146959A/en
Priority to GB9314518A priority patent/GB2267355B/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G15/00Apparatus for electrographic processes using a charge pattern
    • G03G15/01Apparatus for electrographic processes using a charge pattern for producing multicoloured copies

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

Abstract

PURPOSE:To perform 2nd development without disordering a 1st toner image by charging a 1st developer electrostatically with a larger electrostatic charging quantity than a 2nd developer and forming a 1st toner image. CONSTITUTION:This dichroic electrophotographing method repeats exposure and development in order on an electrostatically charged photosensitive body by using developers of two colors to form toner image of the two colors, which are transferred together to a transfer medium and fixed. This dichroic electrophotographing method charges the 1st developer electrostatically with the larger electrostatic charging quantity than the 2nd developer to form the 1st toner image. Thus, the 1st developer which is imparted a larger electrostatic charging quantity sticks strongly on the photosensitive body, so the 1st toner image formed with it is seldom disordered even in the 2nd development. The difference in electrostatic charging quantity between the 1st and 2nd developers is preferably >=3 muc/g in absolute value and the absolute value of the electrostatic charging quantity of the 1st developer is adjusted preferably within a 10-30 muc/g range.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、2色の現像剤を用い、帯電された感光体トに
順次露光と現像を繰り返して2色のトナー像を形成し、
転写媒体上に一括転写して定着させる2色電子写真法に
関する。
Detailed Description of the Invention (Industrial Application Field) The present invention uses two-color developers to sequentially repeat exposure and development on a charged photoconductor to form a two-color toner image.
The present invention relates to a two-color electrophotographic method for transferring and fixing all at once onto a transfer medium.

(従来の技術) 近年カラー現像剤を用いたコピーマシンが開発されてい
る。l−’ X −5030のように一枚のフビー画像
中に2色の現像剤を用い、露光、現像、転写をそれぞれ
繰り返して2色のカラーコピーを得る方法もある。この
方法は、露光、現像、転写の各工程を繰り返すために、
コピー時間が長くなるという欠点があった。
(Prior Art) Copy machines using color developers have been developed in recent years. There is also a method, such as L-' This method repeats the steps of exposure, development, and transfer.
There was a drawback that the copying time was long.

そこで、感光体−ヒに2色の現像剤で露光と現像を繰り
返してトナー像を形成した後、転写媒体に一括転写する
方法が開発された(特願昭63−138399号)。
Therefore, a method has been developed in which a toner image is formed on a photoreceptor by repeating exposure and development with two color developers, and then the toner image is transferred all at once to a transfer medium (Japanese Patent Application No. 138399/1983).

(発明が解決しようとする課題) しかし、この種の方法は、磁気ブラシなどを用いる接触
現像のため、第、1の現像剤により形成される感光体−
ヒのトナー像が、第2の現像時にこすられて、像乱れを
生じ、画質の低下を来す原因となっていた。
(Problems to be Solved by the Invention) However, this type of method uses a magnetic brush or the like for contact development, so the photoreceptor formed by the first developer -
The toner image of H is rubbed during the second development, causing image disturbance and deterioration of image quality.

本発明は、上記の問題点を解消し、第1のトナー像を乱
すことなく、第2の現像を行うことのできる2色電子写
真法を提供しようとするものである。
The present invention aims to solve the above-mentioned problems and provide a two-color electrophotographic method in which the second development can be performed without disturbing the first toner image.

(課題を解決するための手段) 本発明は、2色の現像剤を用い、帯電された感光体上に
順次露光と現像を繰り返して2色のトナー像を形成し、
転写媒体に一括転写して定着させる2色電子写真法にお
いて、第1の現像剤に対して第2の現像剤より高い帯電
量を付与して第1のトナー像を形成することを特徴とす
る2色電子写真法である。
(Means for Solving the Problems) The present invention uses two-color developers to sequentially repeat exposure and development on a charged photoreceptor to form a two-color toner image,
In a two-color electrophotographic method in which a toner image is transferred and fixed at once to a transfer medium, a first toner image is formed by imparting a higher charge amount to a first developer than a second developer. It is a two-color electrophotographic method.

(作用) このように、より高い帯電量が付与された第1の現像剤
は、感光体上により強く付着するので、そこに形成され
る第1のトナー像は、第2の接触現像によっても像乱れ
を生ずることが少ない。
(Function) In this way, the first developer to which a higher amount of charge is applied adheres more strongly to the photoreceptor, so that the first toner image formed thereon is also affected by the second contact development. Image disturbance is less likely to occur.

第1の現像剤と第2の現像剤の帯電量の差は、絶対値で
3μc/g以上とすることが好ましく、また、第1の現
像剤の帯電量は、絶対値で10〜30μc/gの範囲で
調整することが、良好な画像を得るためには好ましい。
It is preferable that the difference in charge amount between the first developer and the second developer is 3 μc/g or more in absolute value, and the charge amount of the first developer is 10 to 30 μc/g in absolute value. It is preferable to adjust within the range of g in order to obtain a good image.

第1の現像剤の帯電量を10μc/gより低くすると、
第2の現像剤の帯電量は7μc/gより低くせざるを得
ず、第2の画像の画像濃度が過剰になったり、J1画像
部のかぶり発生等の不都合が牛する。また、第1の現像
剤の帯電i0を30μc/gより高くすると、第1の画
像濃度が十分に得られない。さらに、第1の現像剤の帯
電量が上記の範囲であっても、第2の現像剤との帯電量
の差が3μC/gより小さいと、第1の画像に線の太り
などが生じて画質の低下を来す。
When the charge amount of the first developer is lower than 10 μc/g,
The amount of charge of the second developer must be lower than 7 μc/g, which leads to problems such as excessive image density of the second image and fogging in the J1 image area. Furthermore, if the charging i0 of the first developer is higher than 30 μc/g, a sufficient first image density cannot be obtained. Furthermore, even if the charge amount of the first developer is within the above range, if the difference in charge amount with the second developer is less than 3 μC/g, thick lines may appear in the first image. Image quality will deteriorate.

なお、第1及び第2の現像剤を逆極性に帯電させること
は、一方の色のトナーが他方の色の現像機に況大して再
度現像される、いわゆるトナー混入を防止する上で好ま
しいが、同極性とすることも可能である。
Note that it is preferable to charge the first and second developers to opposite polarities in order to prevent so-called toner contamination, in which toner of one color is developed again in a developing machine of the other color. It is also possible to have the same polarity.

現像剤の帯電量の調整は、トナー中の帯電制御剤並びに
外添剤の種類と添加量、また、トナーの結着樹脂の種類
、さらには、キャリヤの種類などの選択により、適宜制
御することができ、特イの制御法に限定されるものでは
ない。
The amount of charge of the developer can be adjusted as appropriate by selecting the type and amount of the charge control agent and external additives in the toner, the type of binder resin in the toner, and the type of carrier. However, it is not limited to the specific control method.

なお、現像剤の帯電量は、シリケミカル(株)装帯電量
測定器(TB−200)を用いて測定した。
The charge amount of the developer was measured using a charge amount measuring device (TB-200) manufactured by Sili Chemical Co., Ltd.

本発明で使用する現像剤として下記のトナーとキャリヤ
で構成することができる。そして、トナーは、着色粒子
に外添剤を被覆して作成することができる。
The developer used in the present invention can be composed of the following toner and carrier. The toner can be prepared by coating colored particles with an external additive.

着色粒子は、着色剤と結着樹脂とを主たる構成成分とし
、結着樹脂は、一般の熱可゛塑性樹脂ならばどのような
ものでも使用できるが、具体的には、スチレン、クロル
スチレン等のスチレン類;エチレン、プロピレン、ブチ
レン、インブチレン等のモノオレフィン類;酢酸ビニル
、プロピオン酸ビニル、安息香酸ビニル、酪酸ビニル等
のビニルエステル類;アクリル酸メチル、アクリル酸エ
チル、アクリル酸ブチル、アクリル酸ドデシル、アクリ
ル酸オクチル、アクリル酸フェニル、メタクリル酸メチ
ル、メタクリル酸エチル、メタクリル酸ブチル、メタク
リル酸ドデシル等のα−メチレン脂肪族モノカルボン酸
のエステル類;ビニルメチルエーテル、ビニルエチルエ
ーテル、ビニルブチルエーテル等のビニルエーテル類;
ビニルメチルケトン、ビニルへキシルケトン、ビニルイ
ソプロペニルケトン等のビニルケトン類などの単独重合
体或は共重合体を例示することができ、特に代表的な結
着樹脂としては、ポリスチレン、スチレンアクリル酸ア
ルキル共重合体、スチレン−メタクリル酸アルキル共重
合体、スチレン−アクリロニトリル共重合体、スチレン
−ブタジェン共重合体、スチレン−無水マレイン酸共重
合体、ポリエチレン、ポリプロピレンを挙げることがで
きる。更に、ポリエステル、ポリウレタン、エポキシ樹
脂、シリコーン樹脂、ポリアミド、変性ロジン、パラフ
ィン、ワックス類を挙げることができる。
The main components of the colored particles are a colorant and a binder resin, and the binder resin can be any general thermoplastic resin, but specifically, styrene, chlorostyrene, etc. Styrenes; monoolefins such as ethylene, propylene, butylene, and imbutylene; vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate; methyl acrylate, ethyl acrylate, butyl acrylate, acrylic Esters of α-methylene aliphatic monocarboxylic acids such as dodecyl acid, octyl acrylate, phenyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, dodecyl methacrylate; vinyl methyl ether, vinyl ethyl ether, vinyl butyl ether Vinyl ethers such as;
Examples include homopolymers or copolymers of vinyl ketones such as vinyl methyl ketone, vinyl hexyl ketone, vinyl isopropenyl ketone, etc. Typical binder resins include polystyrene, styrene alkyl acrylate copolymers, etc. Examples include styrene-alkyl methacrylate copolymer, styrene-acrylonitrile copolymer, styrene-butadiene copolymer, styrene-maleic anhydride copolymer, polyethylene, and polypropylene. Further examples include polyester, polyurethane, epoxy resin, silicone resin, polyamide, modified rosin, paraffin, and waxes.

また、着色剤としては、特に限定されるものではないが
、例えば、カーボンブラック、ニグロシン染料、アニリ
ンブルー、カルフィルブルー、クロムイエロー、ウルト
ラマリンブルー、デュポンオイルレッド、キノリンイエ
ロー、メチレンブルー −クロリド、フタロシアニンブルー、マラカイトグリー
ンオキサレート、ランプブラック、ローズベンガル、C
,l、ピグメント・レッド48:I、C,!、ピグメン
ト・レッド122、C,!、ピグメン1−・レッド57
:ISC,I ピグメント・イエロー97、C,1,ピ
グメント・イエロー12、C,1,ピグメント・ブルー
15=1、C,!。
Colorants include, but are not limited to, carbon black, nigrosine dye, aniline blue, Calfil blue, chrome yellow, ultramarine blue, DuPont oil red, quinoline yellow, methylene blue chloride, phthalocyanine. Blue, malachite green oxalate, lamp black, rose bengal, C
, l, Pigment Red 48: I, C,! , Pigment Red 122, C,! , Pigmen 1-Red 57
:ISC,I Pigment Yellow 97,C,1,Pigment Yellow 12,C,1,Pigment Blue 15=1,C,! .

ピグメント・ブルー15二3等を代表的なものとして例
示することができる。
Pigment Blue 1523 can be exemplified as a representative example.

また、着色粒子中に一般的な帯電制御剤を含有させるこ
ともできる。例えば、含クロム染料のような染料類、セ
チルピリジウムクロライド、テトラフェニルボレートカ
リウム塩等のイオン構造をもつものなどを代表的なもの
として挙げることができる。
Further, a general charge control agent can also be contained in the colored particles. Typical examples include dyes such as chromium-containing dyes, and dyes with ionic structures such as cetylpyridium chloride and tetraphenylborate potassium salt.

本発明の着色粒子の体積平均粒径は、約30μmより小
さいものが使用されるが、3〜20μmの範囲のものが
好ましい。
The volume average particle diameter of the colored particles of the present invention is preferably less than about 30 μm, but is preferably in the range of 3 to 20 μm.

上記着色粒子には、更にシリカ微粉末などを外添するこ
とができる。シリカ微粉末には、シリカ微粒子そのもの
、或は、特公昭54−16219号公報に記載の、ケイ
素−炭素結合によって直接に結合している1〜3個の有
機基を有するケイ素原子が、ケイ素−酸素一ケイ素結合
を介して化学的に結合しており、かかるケイ素原子を表
面に有する二硫化ケイ素粒子を挙げることができる。シ
リカ微粒子は疎水性表面処理が施されていてもよい。
Further, fine silica powder or the like can be externally added to the colored particles. The silica fine powder contains the silica fine particles themselves, or silicon atoms having 1 to 3 organic groups directly bonded through silicon-carbon bonds, as described in Japanese Patent Publication No. 54-16219. Examples include silicon disulfide particles that are chemically bonded via oxygen-silicon bonds and have such silicon atoms on their surfaces. The silica fine particles may be subjected to a hydrophobic surface treatment.

また、クリーニング助剤を外添してもよい。クリーニン
グ助剤としては、ポリフッ化ビニリデン粉末、ポリメタ
クリル酸メチル粉末などを挙げることができるが、これ
らに限定されるものではない。
Additionally, a cleaning aid may be added externally. Examples of cleaning aids include, but are not limited to, polyvinylidene fluoride powder, polymethyl methacrylate powder, and the like.

次に、キャリヤ粒子としては、平均粒径500μ口まで
の粒子を用いることができ、例えば、鉄、ニッケル、コ
バルト、酸化鉄、フェライト、ガラスピーズ、粒状シリ
コン等を用いることができる。
Next, as the carrier particles, particles having an average particle diameter of up to 500 μm can be used, and for example, iron, nickel, cobalt, iron oxide, ferrite, glass beads, granular silicon, etc. can be used.

また、これらの粒子の表面にフッ素系樹脂、シリコン樹
脂等の被覆剤で被覆して用いることもできる。
Furthermore, the surfaces of these particles can be coated with a coating agent such as fluororesin or silicone resin.

(実施例1) 第1現像用青色現像剤の作成 スチレン−n−ブチルメタクリレ−1・共重合体(70
/30)  100重量部銅フタロシアニン     
    10重量部カヤチャージN−3(日本化薬製、
負帯電防Iに剤)1重量部 」―記成分を溶融混練した後、微粉砕し、分級して平均
粒径I2μm青色粒子を得た。
(Example 1) Creation of blue developer for first development Styrene-n-butyl methacrylate-1 copolymer (70
/30) 100 parts by weight copper phthalocyanine
10 parts by weight Kaya Charge N-3 (manufactured by Nippon Kayaku,
After melting and kneading 1 part by weight of the components listed above, the components were pulverized and classified to obtain blue particles with an average particle diameter of 2 μm.

この青色粒子100重量部と疎水性シリカ(日本アエロ
ジル(株)製R972)1重量部をヘンシェルミキサー
で混合して負帯電の青色トナーを得た。
100 parts by weight of the blue particles and 1 part by weight of hydrophobic silica (R972 manufactured by Nippon Aerosil Co., Ltd.) were mixed in a Henschel mixer to obtain a negatively charged blue toner.

−・方、平均粒径100μmのフェライトコア上にメチ
ルメタクリレート−n−ブチルメタクリレート共重合体
(80720)を被覆したキャリヤ100重量部と、上
記の青色トナー4重量部とを、V型混合機で混合して第
1の現像用青色現像剤を作成した。
- On the other hand, 100 parts by weight of a carrier made of a ferrite core with an average particle size of 100 μm coated with methyl methacrylate-n-butyl methacrylate copolymer (80720) and 4 parts by weight of the above blue toner were mixed in a V-type mixer. A first blue developer was prepared by mixing.

第2現像用黒色現像剤の作成 スチレン−ローブチルメタクリレート 共重合体(70/30)  101H1f量部カーボン
ブラック         tom蛍部上部セチルピリ
ジウムクロライド  HR11部上記成分を溶融混練し
た後、微粉砕し、分級して平均粒径12μm黒色粒子を
得た。
Preparation of black developer for second development Styrene-lobyl methacrylate copolymer (70/30) 101H1f parts Carbon black Tom Hotarube upper part Cetylpyridium chloride 11 parts HR After melt-kneading the above components, finely pulverize and classify Black particles with an average particle size of 12 μm were obtained.

この黒色粒子100重量部とアルミニウムオキサイドC
(日本アエロジル(株)製)0.5重量部をヘンシェル
ミキサーで混合して正帯電の黒色トナーを得た。
100 parts by weight of the black particles and aluminum oxide C
(manufactured by Nippon Aerosil Co., Ltd.) was mixed in a Henschel mixer to obtain a positively charged black toner.

一方、平均粒径100μmのフェライトコア上にフッ化
ビニリデン−トリフルオロエチレン共重合体(75/2
5)を被覆したキャリヤ100重量部と、上記の黒色ト
ナー5重量部とを、V型混合機で混合して第2の現像用
黒色現像剤を作成した。
On the other hand, vinylidene fluoride-trifluoroethylene copolymer (75/2
A second black developer was prepared by mixing 100 parts by weight of the carrier coated with 5) and 5 parts by weight of the above black toner using a V-type mixer.

(実施例2) 実施例1で得た青色粒子100重量部とシリカ(11本
アエロジル(株)製R972) 2重量部とをヘンシェ
ルミキサーで混合して負帯電の青色トナーを得た。
(Example 2) 100 parts by weight of the blue particles obtained in Example 1 and 2 parts by weight of silica (11 particles R972 manufactured by Aerosil Co., Ltd.) were mixed in a Henschel mixer to obtain a negatively charged blue toner.

その後、実施例1と同様にして第1の現像用青現像剤を
作成した。
Thereafter, a first blue developer was prepared in the same manner as in Example 1.

また、第2の現像用黒現像剤は実施例1のものを用いた
Further, the second black developer used in Example 1 was used.

(実施例3) 0 実施例1で得た青色粒子100重量部とシリカ(日本ア
エロジル(株)製R972) 1重量部及び酸化錫微粉
末1重量部とをヘンシェルミキサーで混合して負帯電の
青色トナーを得た。その後は実施例1と同様にして第1
の現像用現像剤を作成した。
(Example 3) 0 100 parts by weight of the blue particles obtained in Example 1, 1 part by weight of silica (R972 manufactured by Nippon Aerosil Co., Ltd.) and 1 part by weight of tin oxide fine powder were mixed in a Henschel mixer to obtain a negatively charged mixture. A blue toner was obtained. After that, in the same manner as in Example 1, the first
A developer for development was prepared.

また、実施例1で得た黒色粒子100重if部とアルミ
ニウムオキサイドC(日本アエロジル(株)製)0.5
重量部と酸化錫微粉末0,5重量部とをヘンシェルミキ
サーで混合して正帯電用黒トナーを得た。
In addition, 100 parts by weight of the black particles obtained in Example 1 and 0.5 parts of aluminum oxide C (manufactured by Nippon Aerosil Co., Ltd.) were added.
Part by weight and 0.5 part by weight of fine tin oxide powder were mixed in a Henschel mixer to obtain a black toner for positive charging.

その後は実施例1と同様にして第2の現像用意現像剤を
作成した。
Thereafter, a second development preparation developer was prepared in the same manner as in Example 1.

(比較例1) 実施例1で得た青色粒子100重111部とシリカ(1
1本アエロジル(株)製R972)1重量部及び酸化錫
微粉末2重量部とをヘンシェルミキサーで混合して負帯
電の青色トナーを得た。その後は、実施例1と同様にし
て第1の現像用青色現像剤を作成した。
(Comparative Example 1) 100 parts by weight of the blue particles obtained in Example 1 and 111 parts by weight of silica (1
1 part by weight of R972 (manufactured by Aerosil Co., Ltd.) and 2 parts by weight of fine tin oxide powder were mixed in a Henschel mixer to obtain a negatively charged blue toner. Thereafter, a first blue developer was prepared in the same manner as in Example 1.

また、第2の現像用黒色現像剤は、実施例1のものを用
いた。
Further, the second black developer used in Example 1 was used.

(比較例2) 実施例1の青色粒子の作成で、カヤチャージN3を2重
量部に変更し、その他は実施例1と同様にして青色粒子
を作成した。この古色粒子100重量部とシリカ(日本
アエロジル(株)製R972)3重量部とをヘンシェル
ミキサーで混合して負帯電の青色トナーを得た。その後
は、実施例1と同様にして第1の現像用青色現像剤を作
成した。
(Comparative Example 2) Blue particles were prepared in the same manner as in Example 1 except that Kayacharge N3 was changed to 2 parts by weight. 100 parts by weight of the old color particles and 3 parts by weight of silica (R972 manufactured by Nippon Aerosil Co., Ltd.) were mixed in a Henschel mixer to obtain a negatively charged blue toner. Thereafter, a first blue developer was prepared in the same manner as in Example 1.

また、第2の現像用黒色現像剤は、実施例1のものを用
いた。
Further, the second black developer used in Example 1 was used.

(比較例3) 実施例1の第2の現像用の黒色粒子に添加するセチルピ
リジウムクロライドを1.7重量部に変更し、その他は
実施例1と同様にして第2の現像用黒色現像剤を作成し
、第1の現像用現像剤は実施例1の青色現像剤を用いた
(Comparative Example 3) A second black developer was produced in the same manner as in Example 1, except that the amount of cetylpyridium chloride added to the black particles for the second developer in Example 1 was changed to 1.7 parts by weight. The blue developer of Example 1 was used as the first developer.

(コピーテスト) 」−記の実施例及び比較例の現像剤の帯電量を測定した
後、2色電子写真用の試作機に現像剤をセットして、コ
ピーテストを行い、第1現像による画像の線の太り、及
び、画像濃度を測定して画質の1 】2 良否を判定した。
(Copy test) After measuring the amount of charge of the developer of the example and comparative example described in ``--, the developer was set in a prototype machine for two-color electrophotography, a copy test was conducted, and the image obtained by the first development was The line thickness and image density were measured to determine whether the image quality was good or bad.

実施例1は、第1現像による画像において線の太りが極
めて僅かであり、該画像の濃度も十分であった。
In Example 1, the line thickness in the image obtained by the first development was extremely slight, and the density of the image was also sufficient.

実施例2は、第1現像による画像の濃度は、許容できる
ものであり、該画像における線の太りは極めて僅かであ
った。
In Example 2, the density of the image obtained by the first development was acceptable, and the line thickness in the image was extremely small.

実施例3は、第1現像による画像における線の太りは許
容できるものであり、画像の濃度も十分であった。
In Example 3, the line thickness in the image obtained by the first development was acceptable, and the image density was also sufficient.

比較例1は、第1現像剤の帯電量が一6μc/gと低い
ために、第1現像による画像の線の太りが顕著であった
In Comparative Example 1, since the charge amount of the first developer was as low as 16 μc/g, lines in the image formed by the first development were noticeably thickened.

比較例2は、第1現像剤の帯電量が一38μc/gと高
すぎるために、画像濃度を十分に得ることができなかっ
た。
In Comparative Example 2, the amount of charge of the first developer was too high at 138 μc/g, and therefore a sufficient image density could not be obtained.

比較例3は、第1現像剤と第2現像剤の帯電量の差が2
μc/gと小さいために、かなりの線の太りが認められ
た。
In Comparative Example 3, the difference in the amount of charge between the first developer and the second developer was 2.
Due to the small value of μc/g, a considerable thickening of the line was observed.

1枢 3 14− (発明の効果) 本発明は、上記構成を採用することにより、2色電子写
真法の第2の接触現像によっても、第1現像の画像に線
の太りを抑制することができ、かつ、所定の画像濃度を
確保して良質の2色画像の形成を可能にした。
1 3 14- (Effects of the Invention) By adopting the above configuration, the present invention makes it possible to suppress line thickening in the first developed image even by the second contact development of the two-color electrophotography method. This makes it possible to form high-quality two-color images by ensuring a predetermined image density.

5 565−5 565-

Claims (3)

【特許請求の範囲】[Claims] (1)2色の現像剤を用い、帯電された感光体上に順次
露光と現像を繰り返し、2色のトナー像を形成し、転写
媒体上に一括転写して定着させる2色電子写真法におい
て、第1の現像剤に対して第2の現像剤より高い帯電量
を付与して第1のトナー像を形成することを特徴とする
2色電子写真法。
(1) In a two-color electrophotographic method in which two-color developers are used to repeatedly expose and develop a charged photoreceptor in sequence to form a two-color toner image, which is then transferred and fixed all at once onto a transfer medium. , a two-color electrophotographic method characterized in that a first developer is given a higher charge amount than a second developer to form a first toner image.
(2)第1の現像剤を第2の現像剤より絶対値で3μc
/gより高く、絶対値で10〜30μc/gの範囲に帯
電させて、第1のトナー像を形成することを特徴とする
請求項(1)記載の2色電子写真法。
(2) The absolute value of the first developer is 3 μc higher than that of the second developer.
2. The two-color electrophotographic method according to claim 1, wherein the first toner image is formed by charging the first toner image to a higher value than 10 to 30 μc/g in absolute value.
(3)逆極性に帯電する2色の現像剤を用いることを特
徴とする請求項(1)又は(2)記載の2色電子写真法
(3) The two-color electrophotographic method according to claim (1) or (2), characterized in that two-color developers charged with opposite polarities are used.
JP1285023A 1989-11-02 1989-11-02 Dichroic electrophotographiing method Pending JPH03146959A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP1285023A JPH03146959A (en) 1989-11-02 1989-11-02 Dichroic electrophotographiing method
GB9021918A GB2238395B (en) 1989-11-02 1990-10-09 Two-color developer for electrophotography
KR1019900015992A KR910010252A (en) 1989-11-02 1990-10-10 Two-color electrophotography
DE4032702A DE4032702A1 (en) 1989-11-02 1990-10-15 TWO-COLOR DEVELOPERS FOR ELECTROPHOTOGRAPHY
GB9314518A GB2267355B (en) 1989-11-02 1993-07-13 Two-color developer for electrophotography

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1285023A JPH03146959A (en) 1989-11-02 1989-11-02 Dichroic electrophotographiing method

Publications (1)

Publication Number Publication Date
JPH03146959A true JPH03146959A (en) 1991-06-21

Family

ID=17686156

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1285023A Pending JPH03146959A (en) 1989-11-02 1989-11-02 Dichroic electrophotographiing method

Country Status (2)

Country Link
JP (1) JPH03146959A (en)
KR (1) KR910010252A (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5325439A (en) * 1976-06-28 1978-03-09 Kanebo Ltd Developer for electrostatic printing
JPS57197569A (en) * 1981-05-29 1982-12-03 Fujitsu Ltd Recorder
JPS57197568A (en) * 1981-05-29 1982-12-03 Fujitsu Ltd Recorder
JPS60159766A (en) * 1984-01-30 1985-08-21 Fujitsu Ltd Color recording device
JPS60247265A (en) * 1984-05-23 1985-12-06 Japan Steel Works Ltd:The Two-color electrophotographic printing method

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5325439A (en) * 1976-06-28 1978-03-09 Kanebo Ltd Developer for electrostatic printing
JPS57197569A (en) * 1981-05-29 1982-12-03 Fujitsu Ltd Recorder
JPS57197568A (en) * 1981-05-29 1982-12-03 Fujitsu Ltd Recorder
JPS60159766A (en) * 1984-01-30 1985-08-21 Fujitsu Ltd Color recording device
JPS60247265A (en) * 1984-05-23 1985-12-06 Japan Steel Works Ltd:The Two-color electrophotographic printing method

Also Published As

Publication number Publication date
KR910010252A (en) 1991-06-29

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