JPS60220356A - Electrophotographic sensitive body - Google Patents

Electrophotographic sensitive body

Info

Publication number
JPS60220356A
JPS60220356A JP7741684A JP7741684A JPS60220356A JP S60220356 A JPS60220356 A JP S60220356A JP 7741684 A JP7741684 A JP 7741684A JP 7741684 A JP7741684 A JP 7741684A JP S60220356 A JPS60220356 A JP S60220356A
Authority
JP
Japan
Prior art keywords
resin
pigment
layer
red
electrophotographic photoreceptor
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
Application number
JP7741684A
Other languages
Japanese (ja)
Other versions
JPH0469782B2 (en
Inventor
Hideki Anayama
秀樹 穴山
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.)
Canon Inc
Original Assignee
Canon Inc
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 Canon Inc filed Critical Canon Inc
Priority to JP7741684A priority Critical patent/JPS60220356A/en
Publication of JPS60220356A publication Critical patent/JPS60220356A/en
Publication of JPH0469782B2 publication Critical patent/JPH0469782B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/14Inert intermediate or cover layers for charge-receiving layers

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)

Abstract

PURPOSE:To enable easy formation of the latent image of a blue original without inserting a filter into a machine body by dispersing a coloring pigment which absorbs effectively <=520nm light of red or yellow, etc. into the binder of an intermediate layer. CONSTITUTION:An inorg. pigment such as zinchromate or org. pigment such as watching red can be effectively used as the red or yellow coloring pigment which absorbs effectively <=520nm light. Curable rubber and thermosetting resin such as polyurethane resin are adequate as the resin for dispersing said coloring pigments. A conductive white pigment such as tin oxide is added together with the coloring pigment to said resin if the formation of the image is made difficult by the increase in residual potential. A resin layer consisting of polyamide or the like which does not contain conductive powder is provided on the resin layer dispersed therein with the pigment powder and an electric charge generating layer and charge transfer layer are formed on the resin layer which does not contain said conductive powder. The electrophotographic sensitive body is thus formed.

Description

【発明の詳細な説明】 本発明は改良された電子写真感光体に関し、さらにくわ
しくは青原稿に対する電子写真感光体上の潜像を鮮明に
する為に電子写真感光体の基体と電荷発生層の間に特定
の中間層を設けた電子写真感光体に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improved electrophotographic photoreceptor, and more particularly, the present invention relates to an improved electrophotographic photoreceptor, and more particularly, in order to sharpen the latent image on the electrophotographic photoreceptor for a blue original, the present invention relates to an improved electrophotographic photoreceptor having a substrate and a charge generation layer. This invention relates to an electrophotographic photoreceptor with a specific intermediate layer provided therebetween.

従来電荷移動層と電荷発生層から成る積層型の電子写真
感光体において、電荷発生!@の分光吸収が500 n
m以下に及ぶ場合、ハロゲンランプなどの一般光源で分
光反射率のピークが500nm以下にあるような青色原
稿を複写すると、電子写真感光体への相対感度が大きく
なり、感光体−トの潜像が黒色原稿に比べて形成しにく
いという欠点がある。
In conventional multilayer electrophotographic photoreceptors consisting of a charge transfer layer and a charge generation layer, charge generation! The spectral absorption of @ is 500n
When copying a blue original with a spectral reflectance peak of 500 nm or less using a general light source such as a halogen lamp, the relative sensitivity to the electrophotographic photoreceptor increases, causing the latent image on the photoreceptor to The disadvantage is that it is more difficult to form than black originals.

青色原稿による潜像を形成させやすくする為にけ感光体
に当たる像露光軸に露光光源の前側の分光波長をカット
するフィルターを入れる事が成されているが、この方法
ではコスト的に割高になるという欠点があった。
In order to make it easier to form a latent image with a blue original, a filter is installed in the image exposure axis that hits the photoconductor to cut off the spectral wavelength in front of the exposure light source, but this method is expensive in terms of cost. There was a drawback.

本発明は上述の欠点を除去し、フィルターを機械本体に
入れる事なく青色原稿の潜像形成が容易にできる電子写
真感光体を提供するものである。
The present invention eliminates the above-mentioned drawbacks and provides an electrophotographic photoreceptor that can easily form a latent image on a blue original without inserting a filter into the main body of the machine.

本発明は電荷発生層の吸収分光分布によらず青色原稿の
潜像形成を容易にする為に電荷発生層と基体の間に中間
層を設けるものである。この中間層は赤色又は黄色等の
520 nm以下の光を効果的に吸収する着色顔料をバ
インダー樹脂に分散させたものである。
The present invention provides an intermediate layer between the charge generation layer and the substrate in order to facilitate the formation of a latent image on a blue original regardless of the absorption spectral distribution of the charge generation layer. This intermediate layer is made by dispersing in a binder resin a colored pigment such as red or yellow that effectively absorbs light of 520 nm or less.

本発明において用いる5 2− Onm以下の光を効果
的に吸収する赤又は黄色の着色顔料としてハシンクロメ
ート、ストロンチウムエロー、ベンガラ、クロムバーミ
リオン、Hg51鉛丹、オーレオリン、カドミウム赤等
の無機顔料又はウオッチングレッド、ファーストエロー
、ピラゾロンレッド等の有機顔料が有効に使用できる。
Inorganic pigments such as hashin chromate, strontium yellow, red iron, chromium vermilion, Hg51 red, aureolin, cadmium red, etc. are used as red or yellow colored pigments that effectively absorb light of 5 2-Onm or less, or Organic pigments such as Watching Red, Fast Yellow, and Pyrazolone Red can be used effectively.

これらの着色顔料を分散する樹脂は、 (a) 基体に対する密着性が強固であること、(b)
 粉体の分散性が良好であること、(C) 耐溶剤性が
十分であること、 などの条件を満たすものであれば使用できるが、特に、
硬化性ゴム、ポリウレタン樹脂、エポキシ樹脂、アルキ
ド樹脂、ポリエステル樹脂、シリコーン樹脂、アクリル
−メラミン樹脂等の熱硬化性樹脂が好適である。
The resin in which these colored pigments are dispersed must (a) have strong adhesion to the substrate; (b)
It can be used as long as it satisfies the following conditions: (C) the powder has good dispersibility and (C) sufficient solvent resistance; however, in particular:
Thermosetting resins such as curable rubber, polyurethane resin, epoxy resin, alkyd resin, polyester resin, silicone resin, and acrylic-melamine resin are suitable.

分散には、ロールミル、ボールミル、振動ボールミル、
アトライター、サンドミル、コロイドミルなどの常法に
よる。塗布には基体がシート状である場合には、ワイヤ
ーバーコード、ブレードコート、ナイフコート、ロール
コート、スクリーンコートなどが適しており、基体が円
筒状である場合には、浸漬塗布法が適している。
For dispersion, roll mills, ball mills, vibrating ball mills,
By conventional methods such as attritor, sand mill, colloid mill, etc. Wire barcode, blade coating, knife coating, roll coating, screen coating, etc. are suitable for coating when the substrate is sheet-shaped, and dip coating is suitable when the substrate is cylindrical. There is.

但し、この中間層を基体に塗布した際にその体積抵抗が
1012Ω・α以上であると電子写真感光体を作成した
際に、残留爾1位の上昇によシ画像形成が困難となる。
However, if this intermediate layer has a volume resistivity of 10<12 >[Omega].alpha. or more when applied to a substrate, it will be difficult to form an image due to the increase in residual resistance when an electrophotographic photoreceptor is prepared.

このような塗料には着色顔料と共に酸化スズのような導
電性白色顔料を加える事が好適である 前述の着色顔料又は着色顔料と導電性白色顔料を分散し
た塗膜の上に電荷発生層を直接、塗布すると電荷発生層
の顔料粒子が微細孔の内に埋没してしまったり、あるい
は感光特性が変化する。そのために、前述の顔料を分散
した樹脂層の上に導電性粉体を含まない樹脂層を設ける
ことが好適である。そのような樹脂としては例えばポリ
ビニルアルコ−2し、ポリビニルメチルエーテル、ポリ
ビニルエチルエーテル、ポリビニルピリジン、ポリビニ
ルピロリドン、ポリエチレンオキシド、ポリアクリル酸
類、メチルセルロース、エチルセルロース、ポリグルタ
ミン酸、カゼイン、ゼラチン、でんぷん等の水溶性樹脂
、ポリアミド樹脂、フェノール樹脂、ポリビニルホルマ
ール、ポリウレタンニジストマー、アルキド樹脂、エチ
レン−酢酸ビニルコポリマー、ビニルピロリドン−酢酸
ビニルコポリマー等の樹脂が挙けられる。本発明者の実
験の結果ではポリアミド樹脂が最適であった。ポリアミ
ド樹脂は線状のポリアミドであり、いわゆるナイロンお
よび共重合ナイロンで代表される。本発明では、溶液状
態で基体の上に塗布することが適しているので、低々い
し非結晶のものが好ましい。かかる樹脂は、2種以上の
ナイロンの原料を混合して共重合により得ることができ
る。
It is preferable to add a conductive white pigment such as tin oxide to such a paint together with a colored pigment.A charge generation layer is directly applied on a coating film in which the above-mentioned colored pigment or a colored pigment and a conductive white pigment are dispersed. When coated, the pigment particles of the charge generation layer may become embedded in the micropores, or the photosensitivity may change. For this reason, it is preferable to provide a resin layer containing no conductive powder on the resin layer in which the pigment is dispersed. Examples of such resins include water-soluble resins such as polyvinyl alcohol-2, polyvinyl methyl ether, polyvinylethyl ether, polyvinyl pyridine, polyvinyl pyrrolidone, polyethylene oxide, polyacrylic acids, methyl cellulose, ethyl cellulose, polyglutamic acid, casein, gelatin, and starch. Resins such as resins, polyamide resins, phenolic resins, polyvinyl formals, polyurethane distomers, alkyd resins, ethylene-vinyl acetate copolymers, and vinylpyrrolidone-vinyl acetate copolymers are exemplified. According to the results of experiments conducted by the present inventor, polyamide resin was optimal. Polyamide resins are linear polyamides, and are typified by so-called nylons and copolymerized nylons. In the present invention, since it is suitable to apply it on the substrate in a solution state, a low-crystalline or non-crystalline one is preferable. Such a resin can be obtained by copolymerizing a mixture of two or more types of nylon raw materials.

ナイロンの原料としては、例えばナイロン6の原料でめ
るカプロラクタムないし6−アミノカプロン酸、ナイロ
ン66、ナイロン610の原料であるヘキサメチレンジ
アミンとアジピン酸、セバシン酸がどのジカルボン酸、
ナイロン11の原料である11−アミノランチカン酸、
ナイロン12の原料であるω−ラウロラクタムないし1
2−アミノドデカン酸などが挙げられる。
Raw materials for nylon include, for example, caprolactam or 6-aminocaproic acid, which is the raw material for nylon 6, dicarboxylic acids such as hexamethylene diamine and adipic acid, and sebacic acid, which are the raw materials for nylon 66 and nylon 610.
11-aminolanticanic acid, a raw material for nylon 11,
ω-laurolactam or 1, which is the raw material for nylon 12
Examples include 2-aminododecanoic acid.

ポリアミド樹脂層の塗布厚は0.3〜2μ程度が好適で
ある。この導電性粉体を含まない樹脂層上に下達の電荷
発生層および電荷輸送層が形成されて電子写真感光体が
得られる。
The coating thickness of the polyamide resin layer is preferably about 0.3 to 2 microns. A lower charge generation layer and a charge transport layer are formed on this resin layer not containing conductive powder to obtain an electrophotographic photoreceptor.

本発明における電荷発生層は、スーダンレッド、ダイア
ンブルー、ジエナスグリーンBなどのアゾ顔料、アルゴ
ールイエロー、ピレンキノン、インダンスレンブリリア
ントバイオレットRRPなどのキノン顔料、キノシアニ
ン顔料、ペリレン顔料、インジゴ、チオインジゴ等のイ
ンジゴ顔料、インドファーストオレンジトナーなどのビ
スベンゾイミダゾール顔料、銅フタロシアニンなどのフ
タロシアニン顔料、キナクドリン顔料等の電荷発生性物
質を、ポリエステル、ポリスチレン、ポリビニルブチラ
ール、ポリビニルピロリドン、メチルセルロース、ポリ
アクリル酸エステル類、セルロースエステルナトノ結着
剤樹脂に分散して形成される。その厚さは0.01〜1
μ、好ましくは0.05〜0.5部程度である。
The charge generation layer in the present invention includes azo pigments such as Sudan Red, Diane Blue, and Jenas Green B, quinone pigments such as Algol Yellow, Pyrenequinone, and Indanthrene Brilliant Violet RRP, quinocyanine pigments, perylene pigments, indigo, thioindigo, and the like. Charge-generating substances such as indigo pigments, bisbenzimidazole pigments such as India Fast Orange toner, phthalocyanine pigments such as copper phthalocyanine, and quinacridine pigments, polyester, polystyrene, polyvinyl butyral, polyvinyl pyrrolidone, methylcellulose, polyacrylic acid esters, and cellulose. Ester is formed by being dispersed in a binder resin. Its thickness is 0.01~1
μ, preferably about 0.05 to 0.5 parts.

また、電荷輸送層は主鎖又は側鎖にアントラセン、ピレ
ン、フェナントレン、コロネンなどの多環芳香族化合物
又はインドール、カルバゾール、オキサゾール、イソオ
キサゾール、チアゾール、イミダゾール、ピラゾール、
オキサジアゾール、ピラゾリン、チアジアゾール、トリ
アゾールなどの含窒素環式化合物を有する化合物、ヒド
ラゾン化合物等の正孔輸送性物質を成膜性のある樹脂に
溶解させて形成される。これは電荷輸送性物質が一般的
に低分子量で、それ自身では成膜性に乏しいためである
。そのような樹脂としては、ポリカーボネート、ポリメ
タクリル酸エステル類、ボリアリレート、ポリスチレン
、ポリエステル、ポリサルホン、スチレン−アクリロニ
トリルコポリマー、スチレン−メタクリル酸メチルコポ
リマー等が挙けられる。電荷輸送層の厚さは5〜20μ
である。
In addition, the charge transport layer may contain polycyclic aromatic compounds such as anthracene, pyrene, phenanthrene, coronene, or indole, carbazole, oxazole, isoxazole, thiazole, imidazole, pyrazole, etc. in the main chain or side chain.
It is formed by dissolving a hole-transporting substance such as a compound having a nitrogen-containing cyclic compound such as oxadiazole, pyrazoline, thiadiazole, or triazole, or a hydrazone compound in a resin that has film-forming properties. This is because the charge transporting substance generally has a low molecular weight and has poor film-forming properties by itself. Examples of such resins include polycarbonates, polymethacrylates, polyarylates, polystyrene, polyesters, polysulfones, styrene-acrylonitrile copolymers, styrene-methyl methacrylate copolymers, and the like. The thickness of the charge transport layer is 5-20μ
It is.

又、本発明は基体として広範な導電性のものから選択す
ることができる。具体的には、アルミニウム、黄銅、ス
テンレス、ニッケルナトの金属をシリンダーやプレート
形状にしたもの、あるいはアルミニウム、酸化インジウ
ム、酸化スズをプラスチックや紙に蒸着又はラミネート
したものなどを挙げることができる。
Additionally, the present invention allows the substrate to be selected from a wide variety of conductive materials. Specifically, examples include metals such as aluminum, brass, stainless steel, and nickel metal formed into a cylinder or plate shape, or metals such as aluminum, indium oxide, and tin oxide deposited or laminated on plastic or paper.

実施例1 基体として60φX2601+1111の、アルミニウ
ムシリンダーを用意した。
Example 1 An aluminum cylinder of 60φ×2601+1111 was prepared as a base.

ベンガラ(ye2oa) lo o部(1量部、以下同
じ)をアクリル樹脂(商品名ニアクリディックA405
、大日本インキ(株)製)80部(固型分50%)、メ
ラミン樹脂(商品名ニス−パーベッカミンL121、大
日本インキ(株)製)20部(固型分60チ)およびト
ルエン100部の溶液に混合し、次いでボールミルによ
り、6時間にわたり分散した。この分散液を上記基体上
に浸漬法で塗布し、150℃で30分間に亘って熱硬化
し、25μ厚の中間層をもうけた。
Red red iron (ye2oa) lo o part (1 part, same hereinafter) is added to acrylic resin (trade name Niacridic A405).
, manufactured by Dainippon Ink Co., Ltd.) 80 parts (solid content 50%), melamine resin (trade name Varnish-Perbeckamine L121, manufactured by Dainippon Ink Co., Ltd.) 20 parts (solid content 60 inches), and 100 parts of toluene. solution and then dispersed in a ball mill for 6 hours. This dispersion was applied onto the above substrate by a dipping method and thermally cured at 150° C. for 30 minutes to form an intermediate layer with a thickness of 25 μm.

次に、共重合ナイロン樹脂(商品名:アミランC!M8
000、東し製)10部(重量部、以下同様)をメタノ
ール60部、ブタノール40部の混合液に溶解し、上記
中間層上に浸漬塗布して、1μ厚のポリアミド樹脂層を
もうけた。
Next, copolymerized nylon resin (product name: Amilan C! M8
000, produced by Toshi) (by weight, hereinafter the same) was dissolved in a mixed solution of 60 parts of methanol and 40 parts of butanol, and the solution was dip coated onto the above intermediate layer to form a polyamide resin layer with a thickness of 1 μm.

次に下記構造式のジスアゾ顔料を10部酢酸酪酸セルロ
ース樹脂(商品名: CAB−381:イーストマン化
学展)6部およびシクロヘキサノン60部を1φガラス
ピーズを用いたサンドミル装置で20時間分散した。こ
の分散液にメチルエチルケトン100部を加えて、上記
ポリアミド樹脂層上に浸漬塗布し、100″Cで10分
間の加熱乾燥をして、0.1 f/fn2の塗布量の電
荷発生層をもうけた。
Next, 10 parts of a disazo pigment having the following structural formula, 6 parts of cellulose acetate butyrate resin (trade name: CAB-381: Eastman Chemical Exhibition), and 60 parts of cyclohexanone were dispersed for 20 hours in a sand mill apparatus using 1φ glass beads. 100 parts of methyl ethyl ketone was added to this dispersion, which was dip coated onto the polyamide resin layer, and dried by heating at 100''C for 10 minutes to form a charge generation layer with a coating weight of 0.1 f/fn2. .

次いで、下記構造式のヒドラゾン化合物を10部 およびスチレン−メタクリル酸メチル共重合樹脂(商品
名:MS200 ;製鉄化学(株)製)15部をトルエ
ン80部に溶解した。この液を上記電荷発生層上に塗布
して100’Cで1時間の熱風乾燥をして、16μ厚の
電荷輸送層を形成し電子写真感光体とした。
Next, 10 parts of a hydrazone compound having the following structural formula and 15 parts of a styrene-methyl methacrylate copolymer resin (trade name: MS200; manufactured by Steel Manufacturing Co., Ltd.) were dissolved in 80 parts of toluene. This liquid was applied onto the charge generation layer and dried with hot air at 100'C for 1 hour to form a charge transport layer with a thickness of 16μ, thereby preparing an electrophotographic photoreceptor.

実施例2 基体は実施例1と同じ物を用いた。クロムパーミリメン
80部と酸化スズ粉体2o部をアクリル樹脂(商品名ニ
アクリディックA4o5、大日本インキ(株)製)80
部(固型分50%)、メラミン樹脂(商品名:スーパー
ペッヵミンL121、大日本インキ(株)製)20部(
固型分60%)およびトルエン100部の溶液に混合し
、次いでボールミルにより、6時間にわたり分散した。
Example 2 The same substrate as in Example 1 was used. 80 parts of chromium permylene and 20 parts of tin oxide powder were mixed with 80 parts of acrylic resin (trade name: Niacridic A4o5, manufactured by Dainippon Ink Co., Ltd.).
(solid content 50%), 20 parts of melamine resin (trade name: Super Peccamin L121, manufactured by Dainippon Ink Co., Ltd.)
(solid content: 60%) and 100 parts of toluene, and then dispersed in a ball mill for 6 hours.

この分散液を基体上に浸漬法で塗布し、150°Cで3
0分間に亘って熱硬化し、25μ厚の中間層をもうけた
This dispersion was applied onto the substrate by dipping, and heated at 150°C for 3 hours.
Heat cured for 0 minutes to create a 25μ thick intermediate layer.

次に、実施例1で用いたポリアミド樹脂層、電荷発生層
および電荷輸送層を順次形成して電子写真感光体を作成
した。
Next, the polyamide resin layer, charge generation layer, and charge transport layer used in Example 1 were sequentially formed to prepare an electrophotographic photoreceptor.

比較例1 実施例1と同じ基体の上に中間層を設けず基体の上に直
接実施例1で用いたポリアミド樹脂層、電荷発生層およ
び電荷輸送層を順次形成して電子写真感光体を作成した
Comparative Example 1 An electrophotographic photoreceptor was prepared by sequentially forming the polyamide resin layer, charge generation layer, and charge transport layer used in Example 1 directly on the same substrate as in Example 1 without providing an intermediate layer. did.

実施例1.2及び比較例1で製造した感光体を−5,6
KVコロナ帯電、画像露光、乾式トナー現像、普通紙へ
のトナー転写、ウレタンゴムブレード(硬度70、圧力
106w72m、感光体に対する角度20°)によるク
リーニング工程等を有する電子写真複写機に取り付けて
感色性の評価を行った。濃度0.3(マクベスRD−5
14濃度測定器使用、以下同様)の原稿を0,5の濃度
に複写できる現像設定において、図面の分光反射率をも
つ青色原稿を複写し、それぞれのコピー濃度を測定した
The photoreceptors manufactured in Example 1.2 and Comparative Example 1 were
It is attached to an electrophotographic copying machine that has KV corona charging, image exposure, dry toner development, toner transfer to plain paper, cleaning process using a urethane rubber blade (hardness 70, pressure 106w72m, angle 20° to the photoconductor), etc. Gender was evaluated. Density 0.3 (Macbeth RD-5
A blue original having the spectral reflectance of the drawing was copied using a development setting that allows copying a 14-density measuring device (the same applies hereinafter) to a density of 0.5, and the density of each copy was measured.

以上説明したように基体と電荷発生層の間に520 n
m以下の短波長光を吸収する顔料を含む中間層を設ける
事によって青色の再現性の良い電子写真感光体を作る事
ができム
As explained above, there is a gap of 520 n between the substrate and the charge generation layer.
By providing an intermediate layer containing a pigment that absorbs light with short wavelengths of less than m, it is possible to create an electrophotographic photoreceptor with good blue reproducibility.

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

図面は青色原稿の分光反射率を示す図である。 The drawing is a diagram showing the spectral reflectance of a blue original.

Claims (1)

【特許請求の範囲】 1 電荷発生層と電荷移動層を有する電子写真感光体に
おいて基体と感光層の間に中間層として、520nm以
下の短波長光を吸収する着色顔料を含んだ樹脂層を設け
た事を特徴とする電子写真感光体。 2 中間層の体積抵抗を下げる為、着色顔料に導電性白
色顔料を加えたことを特徴とする特許請求の範囲第1項
に記載の電子写真感光体。
[Scope of Claims] 1. In an electrophotographic photoreceptor having a charge generation layer and a charge transfer layer, a resin layer containing a colored pigment that absorbs short wavelength light of 520 nm or less is provided as an intermediate layer between the substrate and the photosensitive layer. An electrophotographic photoreceptor characterized by the following. 2. The electrophotographic photoreceptor according to claim 1, characterized in that a conductive white pigment is added to the colored pigment in order to lower the volume resistance of the intermediate layer.
JP7741684A 1984-04-17 1984-04-17 Electrophotographic sensitive body Granted JPS60220356A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7741684A JPS60220356A (en) 1984-04-17 1984-04-17 Electrophotographic sensitive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7741684A JPS60220356A (en) 1984-04-17 1984-04-17 Electrophotographic sensitive body

Publications (2)

Publication Number Publication Date
JPS60220356A true JPS60220356A (en) 1985-11-05
JPH0469782B2 JPH0469782B2 (en) 1992-11-09

Family

ID=13633336

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7741684A Granted JPS60220356A (en) 1984-04-17 1984-04-17 Electrophotographic sensitive body

Country Status (1)

Country Link
JP (1) JPS60220356A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63188144A (en) * 1987-01-30 1988-08-03 Konica Corp Photosensitive body

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63188144A (en) * 1987-01-30 1988-08-03 Konica Corp Photosensitive body

Also Published As

Publication number Publication date
JPH0469782B2 (en) 1992-11-09

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