JPS62192750A - Electrophotographic sensitive body - Google Patents

Electrophotographic sensitive body

Info

Publication number
JPS62192750A
JPS62192750A JP3276186A JP3276186A JPS62192750A JP S62192750 A JPS62192750 A JP S62192750A JP 3276186 A JP3276186 A JP 3276186A JP 3276186 A JP3276186 A JP 3276186A JP S62192750 A JPS62192750 A JP S62192750A
Authority
JP
Japan
Prior art keywords
carrier
layer
photosensitive layer
parts
electrophotographic
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
JP3276186A
Other languages
Japanese (ja)
Other versions
JPH0469951B2 (en
Inventor
Masaru Hasegawa
勝 長谷川
Osamu Suda
須田 修
Toshio Kono
寿夫 河野
Norio Tanaka
教雄 田中
Tetsuhiro Umezaki
梅嵜 哲博
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.)
Dainichiseika Color and Chemicals Mfg Co Ltd
Original Assignee
Dainichiseika Color and Chemicals Mfg 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 Dainichiseika Color and Chemicals Mfg Co Ltd filed Critical Dainichiseika Color and Chemicals Mfg Co Ltd
Priority to JP3276186A priority Critical patent/JPS62192750A/en
Publication of JPS62192750A publication Critical patent/JPS62192750A/en
Publication of JPH0469951B2 publication Critical patent/JPH0469951B2/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
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0664Dyes
    • G03G5/0675Azo dyes
    • G03G5/0687Trisazo dyes
    • G03G5/0688Trisazo dyes containing hetero rings

Abstract

PURPOSE:To provide excellent electrophotographic characteristics by providing a photosensitive layer contg. a specific trisazo compd. on a conductive substrate. CONSTITUTION:The photosensitive layer contg. the trisazo compd. expressed by the formula is provided on the conductive substrate. The lamination of a carrier generating layer essentially consisting of the trisazo compd. Which is a carrier generating material and a carrier transfer layer essentially consisting of a carrier transfer material on the conductive substrate is the preferable physical constitution of this electrophotographic sensitive body. The provision of the photosensitive layer formed by dispersing the carrier generating material in the carrier transfer material is equally preferable. The electrophotographic characteristics such as electrostatic change characteristic, electric charge holding power, sensitivity and residual potential are improved by utilizing the excellent carrier generating function which the trisazo compd. expressed by the formula possesses.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は電子写真感光体に関し、4.4”。[Detailed description of the invention] (Industrial application field) The present invention relates to an electrophotographic photoreceptor having a size of 4.4".

4″−トリアミノ−ベンジルジフェニルアミンをジアゾ
成分に用いたトリスアゾ化合物を含有する感光層を設け
た新規な電子写真感光体を提供する。
Provided is a novel electrophotographic photoreceptor provided with a photosensitive layer containing a trisazo compound using 4''-triamino-benzyldiphenylamine as a diazo component.

(従来の技術およびその問題点) 近年、電子写真方式の利用は、複写機の分野に限らず、
印刷版材、スライド、フィルム、マイクロフィルム等の
従来は写真技術が使われていた分野へも広がり、またレ
ーザやCRTを光源とする高速プリンターへの応用も検
討されている。従って電子写真感光体に対する要求も、
高度で幅広いものになりつつある。
(Prior art and its problems) In recent years, the use of electrophotography is not limited to the field of copying machines.
It has spread to fields where photographic technology has traditionally been used, such as printing plates, slides, film, and microfilm, and application to high-speed printers that use lasers or CRTs as light sources is also being considered. Therefore, the requirements for electrophotographic photoreceptors are
It is becoming more advanced and wide-ranging.

これまで電子写真方式に用いる感光体とじては、非晶質
セレン、硫化カドミウム、酸化亜鉛等の無機光導電性物
質を主成分とする感光層を有するものが主体であった。
Until now, photoreceptors used in electrophotography have mainly had photosensitive layers containing inorganic photoconductive substances such as amorphous selenium, cadmium sulfide, and zinc oxide.

これらの無機物質からなる感光体は有用なものではある
が、一方でさまざまな欠点もある。
Although photoreceptors made of these inorganic materials are useful, they also have various drawbacks.

近年これを補うため、種々の有機物質を光導電性物質と
して用いた電子写真感光体が提案され、実用に供され始
めた。電子写真感光体はいうまでもなく、キャリア発生
機能とキャリア輸出機能とを有しなければならない、キ
ャリア発生物質として使用できる有機化合物としては、
フタロシアニン系、多環牛ノン系、インジゴ系、ジオキ
サジン系、キナクリドン系、アゾ系等数多くの顔料が提
案されているが、実用化に至ったものはごく限られてい
る。またキャリア移動物質の選択の範囲も限定されてい
るので、電子写真プロセスの幅広い要求に充分こたえら
れるものはまだ得られていないのが現状である。
In recent years, in order to compensate for this problem, electrophotographic photoreceptors using various organic substances as photoconductive substances have been proposed and have begun to be put into practical use. Needless to say, electrophotographic photoreceptors must have a carrier generation function and a carrier export function, and organic compounds that can be used as carrier generation substances include:
Many pigments have been proposed, including phthalocyanine, polycyclic bovine non-, indigo, dioxazine, quinacridone, and azo pigments, but only a limited number of them have been put into practical use. Furthermore, since the range of selection of carrier transfer substances is limited, it is currently not possible to obtain a substance that satisfactorily meets the wide range of demands of electrophotographic processes.

(問題を解決するための手段) 本発明者らは有機電子写真感光体を改良すべく鋭意研究
の結果、4 、4 ” 、 4 ” −トリアミノ−ベ
ンジルジフェニルアミンをジアゾ成分に用いたトリスア
ゾ化合物を含有する感光層を設けたものが優れた電子写
真特性を有することを見出して本発明に至った。
(Means for Solving the Problem) As a result of intensive research to improve organic electrophotographic photoreceptors, the present inventors have developed a trisazo compound containing 4,4'',4''-triamino-benzyldiphenylamine as a diazo component. The present inventors have discovered that a photosensitive layer provided with a photosensitive layer has excellent electrophotographic properties, and have arrived at the present invention.

すなわち、本発明は、導電性支持体に上に下記の一般式
(I)で示されるトリスアゾ化合物を含有する感光層を
設けたことを特徴とする電子写真感光体である。
That is, the present invention is an electrophotographic photoreceptor characterized in that a photosensitive layer containing a trisazo compound represented by the following general formula (I) is provided on a conductive support.

但し、上記式中Aは、一般式 または非置換のアルキル基、芳香族炭化水素基あるいは
芳香族複素環基を表わす。
However, in the above formula, A represents a general formula or an unsubstituted alkyl group, an aromatic hydrocarbon group, or an aromatic heterocyclic group.

−115を式(I)で表わされる化合物の具体例として
は、例えば次の如き化合物が挙げられる(尚一般式(D
の化合物のAの基Rで表わした)。
Specific examples of compounds in which -115 is represented by the formula (I) include the following compounds (in addition, the general formula (D
(represented by the group R of A of the compound).

No、Hの 1)  メチル             32)  
イソプロピル           33)   n−
ブチル           44) シクロヘキシル
         45) フェニル        
    36)2−メチル111        37
)4−メトキシ111        38)3−ニト
ロiti        49)   3−)リフルオ
ロメチル     410)l−ナフチル      
     311)   2.5−ジメトキシ−4−フ
ェニ 3ルカルバモイル111 12)   2,4.5−トリクロル111  313
)   2.5−ジメトキシ−4−クロル 414)2
−ピリジル           415)2−チアゾ
リル         41B)5−メチルベンゾチア
ゾール−24−イル 本発明の電子写真感光体は、上記一般式(I)で示され
るトリスフジ化合物の持つ優れたキャリア発生機能を、
いわゆる積層型または分散型の電子写真感光体の苓ヤリ
ア発生物質として利用することにより、帯電特性、電荷
保持力、感度、残留電位等の電子写真特性に優れるばか
りでなく、被膜物性が良好で、繰り返し使用による劣化
が少なく、熱、湿度、光に対しても諸特性が変化せず安
定した性能を発揮できる感光体である。
No, H 1) Methyl 32)
Isopropyl 33) n-
Butyl 44) Cyclohexyl 45) Phenyl
36) 2-methyl 111 37
) 4-methoxy111 38) 3-nitroiti 49) 3-) Lifluoromethyl 410) l-naphthyl
311) 2,5-dimethoxy-4-pheny3carbamoyl 111 12) 2,4,5-trichlor 111 313
) 2,5-dimethoxy-4-chlor 414)2
-Pyridyl 415) 2-thiazolyl 41B) 5-methylbenzothiazol-24-yl The electrophotographic photoreceptor of the present invention has the excellent carrier generation function of the trisfuji compound represented by the above general formula (I),
By using it as a layer-generating material in so-called laminated or dispersion type electrophotographic photoreceptors, it not only has excellent electrophotographic properties such as charging characteristics, charge retention, sensitivity, and residual potential, but also has good film properties. It is a photoreceptor that exhibits little deterioration due to repeated use and exhibits stable performance without changing its characteristics even when exposed to heat, humidity, or light.

上記の化合物は公知の方法で合成できる。まず、4 、
4 ” 、 4 ” −)リアミノーベンジルジ ・フ
ェニルアミンを常法によりジアゾ化し、生じたトリスジ
アゾニウム塩をカップリング成分とカップリングさせ、
一般式(I)で示される構造を持つトリスアゾ化合物を
得る。以下に合成例の1例を挙げるが、他の一般式(1
)で示される構造を持つトリスアゾ化合物も下記の合成
例に準じて合成できる。尚、以下の合成例において1部
」または「%」は各々重量部または重量%を示す。
The above compounds can be synthesized by known methods. First, 4,
4'', 4''-) riaminobenzyldi-phenylamine is diazotized by a conventional method, and the resulting trisdiazonium salt is coupled with a coupling component,
A trisazo compound having a structure represented by general formula (I) is obtained. One example of synthesis is given below, but other general formula (1
) can also be synthesized according to the synthesis example below. In the following synthesis examples, "1 part" or "%" indicates parts by weight or % by weight, respectively.

丸底町(例示化合物1の場合) 4 、4 ′、 4− トリアミノ−ベンジルジフェニ
ルアミン14.5部を水300部と35%濃塩酸63部
に分散し、この液を0〜5℃に保ち、よ〈撹拌しなから
10%亜硝酸ナトリウム水溶液115部を10分間を要
して滴下し、滴下終了後更に15分間撹拌してジアゾニ
ウム塩溶液を得る。
Marusokocho (for Exemplary Compound 1) 14.5 parts of 4,4',4-triamino-benzyldiphenylamine was dispersed in 300 parts of water and 63 parts of 35% concentrated hydrochloric acid, and this liquid was maintained at 0 to 5°C. 115 parts of a 10% aqueous sodium nitrite solution was added dropwise over 10 minutes without stirring, and after the addition was complete, the mixture was stirred for an additional 15 minutes to obtain a diazonium salt solution.

3−ヒドロキシN−メチルナフタルイミド34.1部を
水酸化ナトリウム水溶液1.000部に溶解した後、冷
却し、0〜5℃に保ちながら上記ジアゾニウム塩溶液を
15分間を要して滴下した0滴下終了後、更に2時間撹
拌し、生じたトリスアゾ化合物を濾別し、充分に洗浄し
て例示化合物lの組成物45.1部を得た。これをDM
F、メタノール、次いで水で順次洗浄、乾燥して精製物
を得た。
After dissolving 34.1 parts of 3-hydroxy N-methylnaphthalimide in 1.000 parts of an aqueous sodium hydroxide solution, the solution was cooled, and the above diazonium salt solution was added dropwise over a period of 15 minutes while maintaining the temperature at 0 to 5°C. After the addition was completed, the mixture was further stirred for 2 hours, and the resulting trisazo compound was filtered off and thoroughly washed to obtain 45.1 parts of a composition of Exemplified Compound 1. DM this
The purified product was sequentially washed with F, methanol, and then water, and dried to obtain a purified product.

本発明の電子写真感光体の物理的構成は、既知の形態の
いずれによってもよい、導電性支持体上に、キャリア発
生物質である上記のトリスアゾ化合物を主成分とするキ
ャリア発生層と、キャリヤー輸送物質を主成分とするキ
ャリア輸送層を積層してもよいし、キャリア発生物質を
キャリヤー輸送物質中に分散させた感光層を設けてもよ
い。
The physical structure of the electrophotographic photoreceptor of the present invention is such that a carrier generation layer containing the above-mentioned trisazo compound as a carrier generation substance as a main component is provided on a conductive support, which may be in any known form, and a carrier generation layer containing the above-mentioned trisazo compound as a carrier generation substance; A carrier transport layer containing a substance as a main component may be laminated, or a photosensitive layer in which a carrier-generating substance is dispersed in a carrier transport substance may be provided.

これらは中間層を介して設けてもよいので次の様なパタ
ーンが可能である。
Since these may be provided through an intermediate layer, the following patterns are possible.

■)導電性支持体/キャリア発生層/キャリア輸送層 II )導電性支持体/キャリア輸送層/キャリア発生
層 ■)導電性支持体/キャリア発生物質を含むキャリア輸
送層 ■)導電性支持体/中間層/キャリア発生層/キャリア
輸送層 ■)導電性支持体/中間層/キャリア輸送層/キャリア
発生層 vT)導電性支持体/中間層/キャリア発生物質を含む
キャリア輸送層 ここで中間層とは、バリア層あるいは接着層の事である
。上記構成の電子写真感光体上に表面保護等の目的で薄
い層を設ける事も可能である。
■) Conductive support/carrier-generating layer/carrier transport layer II) Conductive support/carrier transport layer/carrier-generating layer ■) Conductive support/carrier transport layer containing a carrier-generating substance ■) Conductive support/ Intermediate layer/carrier generation layer/carrier transport layer■) Conductive support/intermediate layer/carrier transport layer/carrier generation layervT) Conductive support/intermediate layer/carrier transport layer containing a carrier generation substance is a barrier layer or adhesive layer. It is also possible to provide a thin layer on the electrophotographic photoreceptor having the above structure for the purpose of surface protection or the like.

キャリヤー輸送物質は、電子の輸送をするものと正孔の
輸送をするものとがあるが、本発明の電子写真感光体の
形成にはどちらも使用できる。
Carrier transport materials include those that transport electrons and those that transport holes, and either can be used to form the electrophotographic photoreceptor of the present invention.

本発明の電子写真感光体は、有機質の光導電性物質を使
用する電子写真感光体の製造において知られている技術
に従って、通常の方法で製造できる0例えば、2層構成
の感光層を形成するキャリア発生層は、前記のトリスア
ゾ化合物を適当な媒体中で微細粒子とし、必要に応じて
バインダーを加え、導電性支持体の上に直接、または中
間層を介して塗布するか、または既に形成したキャリア
輸送層の上に塗布し、乾燥する。
The electrophotographic photoreceptor of the present invention can be manufactured by a conventional method according to techniques known in the manufacture of electrophotographic photoreceptors using organic photoconductive materials.For example, a two-layer photoreceptor layer is formed. The carrier generation layer is prepared by forming the trisazo compound into fine particles in a suitable medium, adding a binder if necessary, and coating the conductive support directly or through an intermediate layer, or by applying the already formed layer to the conductive support. Coat on top of the carrier transport layer and dry.

媒体中の微細粒子は、径5ILm以下、好ましくは34
m、最適にはlJLmにして分散させる必要がある。
The fine particles in the medium have a diameter of 5 ILm or less, preferably 34
m, and optimally lJLm.

バインダーを用いる場合、特に限定はないが疎水性で、
誘導率が高く、電気絶縁性のフィルム形成高分子化合物
が好ましい、各種の熱可塑性または熱硬化性の合成樹脂
が好適に使用できる。容易に理解されるとおり、前記の
媒体はバインダーを溶解する能力をもつと好都合である
。バインダーの使用量は、前記キャリア発生物質に対し
、重量で0.1〜5倍の範囲からえらぶ。
When using a binder, there are no particular limitations, but it must be hydrophobic,
Various thermoplastic or thermosetting synthetic resins can be suitably used, with film-forming polymeric compounds having high dielectric properties and electrical insulation properties being preferred. As will be readily understood, it is advantageous for the medium to have the ability to dissolve the binder. The amount of the binder to be used is selected from a range of 0.1 to 5 times the weight of the carrier generating substance.

キャリア発生層の膜厚は、0.O1〜20pmの範囲と
する。好ましくは0.05〜5μmである。キャリア輸
送層は、キャリヤー輸送物質を適当な媒体に分散あるい
は溶解して塗布し乾燥することにより形成できる。キャ
リヤー輸送物質が、ポリ−N−ビニルカルバゾールやポ
リグリシジルカルバゾールの様な、それ自身でバインダ
ーの役割をも果すものを使用する場合を除き、バインダ
ーを使用することが好ましい、バインダーとしては、キ
ャリア発生層の形成に使用するバインダーと同種のもの
が使用できる。バインダーの使用量は、キャリヤー輸送
物質の0.2〜5重量倍が適当である。キャリア輸送層
の膜厚は、1〜1100Bの範囲とするが、好ましくは
5〜50JLmである。
The carrier generation layer has a thickness of 0. The range is O1 to 20pm. Preferably it is 0.05 to 5 μm. The carrier transport layer can be formed by dispersing or dissolving a carrier transport substance in a suitable medium, coating the mixture, and drying the mixture. It is preferable to use a binder, unless the carrier transport substance also acts as a binder itself, such as poly-N-vinylcarbazole or polyglycidylcarbazole. The same type of binder as used for forming the layer can be used. The appropriate amount of binder to be used is 0.2 to 5 times the weight of the carrier transport material. The thickness of the carrier transport layer is in the range of 1 to 1100 B, preferably 5 to 50 JLm.

一方1分散型のキャリア発生層−キャリア輸送層を形成
するには、上述のキャリア発生層形成用の分散液に、キ
ャリヤー輸送物質を溶解させて、導電性支持体上に塗布
すればよい、キャリヤー輸送物質は任意にえらべるが、
前記したような、それ自身バイングーとして役立つもの
を使用する場合は別として、一般にバインダーを添加す
ることが好ましい、導電性支持体と上記の積層型または
分散型の感光層の間に中間層を設ける場合、中間層には
キャリア発生物質、キャリヤー輸送物質。
On the other hand, in order to form a one-dispersion type carrier generation layer-carrier transport layer, a carrier transport substance may be dissolved in the above-mentioned dispersion liquid for forming a carrier generation layer, and then applied onto a conductive support. Transport substances can be selected arbitrarily, but
Apart from the use of materials which themselves serve as binders as described above, an intermediate layer is provided between the conductive support and the above-mentioned laminated or dispersed photosensitive layer, to which it is generally preferred to add a binder. In this case, the intermediate layer contains a carrier-generating substance and a carrier-transporting substance.

バインダー、添加剤等の1種あるいは2種以上の混合物
でしかも中間層としての機能を損わない範囲で常用の材
料を用いることができる。膜厚は10gm以下で好まし
くはIBm以下が良い。
One type or a mixture of two or more types of binders, additives, etc., and commonly used materials can be used as long as the function as an intermediate layer is not impaired. The film thickness is preferably 10 gm or less, preferably IBm or less.

本発明の電子写真感光体は、このほかにも既知の技術を
適用することもできる0例えば感光層は増感剤を含んで
いてもよい、好適な増感剤は、有機光導電性物質と電荷
移動錯体を形成するルイス酸や染料色素等が挙げられる
。また感光層の成膜性、他線性、機械的強度等を向上さ
せるために必要に応じて可塑剤、紫外線吸収剤、酸化防
止剤、滑剤、接着促進剤、分散剤等の添加剤を加えても
よく、本発明の目的とする電子写真感光体特性を損なわ
ない範囲でキャリア発生物質、キャリヤー輸送物質を加
えてもよい。
In addition to this, the electrophotographic photoreceptor of the present invention may be manufactured using known techniques. For example, the photosensitive layer may contain a sensitizer. Preferred sensitizers include an organic photoconductive substance and a sensitizer. Examples include Lewis acids and dyes that form charge transfer complexes. In addition, additives such as plasticizers, ultraviolet absorbers, antioxidants, lubricants, adhesion promoters, dispersants, etc. may be added as necessary to improve film formability, linearity, mechanical strength, etc. of the photosensitive layer. Alternatively, a carrier-generating substance and a carrier-transporting substance may be added to the extent that they do not impair the properties of the electrophotographic photoreceptor aimed at in the present invention.

本発明においては、キャリア発生層、キャリア輸送層、
更に中間層あるいは表面層の形成方法として、通常の塗
布方法を用いることができる。
In the present invention, a carrier generation layer, a carrier transport layer,
Furthermore, a conventional coating method can be used to form the intermediate layer or surface layer.

本発明の電子写真感光体は、次に掲げる実施例からも明
らかなように、帯電特性、感度特性、画像形成性におい
て優れており、感光性も良好であり、また繰り返し使用
しても感度や帯電特性の変動が小さく、光疲労も少ない
、耐候性も高い。
As is clear from the following Examples, the electrophotographic photoreceptor of the present invention has excellent charging characteristics, sensitivity characteristics, and image forming properties, and has good photosensitivity. It has small fluctuations in charging characteristics, low optical fatigue, and high weather resistance.

次に実施例を挙げて本発明を更に具体的に説明する0文
中「部」とあるのは重量部をあられす。
Next, the present invention will be explained in more detail with reference to Examples. In the following sentences, "parts" refer to parts by weight.

突JLfLユ 前記例示化合物1)1部とポリエステル樹脂(東洋紡「
バイロン200J)1部をテトラヒドロフラン50部中
に入れてボールミルで充分に分散させ、分散液をワイヤ
ーコーターでアルミニウム板上に塗布し、120℃の熱
風で30分間乾燥して、膜厚が0.31Lmのキャリア
発生層を設けた。
1 part of the above-mentioned exemplified compound 1) and polyester resin (Toyobo "
Put 1 part of Vylon 200J) into 50 parts of tetrahydrofuran and thoroughly disperse it with a ball mill.The dispersion was applied onto an aluminum plate with a wire coater and dried with hot air at 120°C for 30 minutes to give a film thickness of 0.31Lm. A carrier generation layer was provided.

その上に、P−ジエチルアミノベンズアルデヒF−N−
フェニル−N−ベンジルヒドラゾン5部とポリカーボネ
ート樹脂(奇人化成「パンライトL−1250J)5部
とを1,2−ジクロエタン70部に溶解した溶液を塗布
し、60℃の温風で3時間乾燥して、M厚141Lmの
キャリア輸送層を形成した。
Furthermore, P-diethylaminobenzaldehyde F-N-
A solution of 5 parts of phenyl-N-benzylhydrazone and 5 parts of polycarbonate resin (Kijin Kasei "Panlite L-1250J" dissolved in 70 parts of 1,2-dichloroethane) was applied and dried with warm air at 60°C for 3 hours. Thus, a carrier transport layer having a thickness of 141 Lm was formed.

このようにして製造した感光板を、25℃、RH(相対
湿度)55%の雰囲気中に放置して、調湿した後、静電
紙試験装置(川口電機製作所「5P−428J)を用い
て、スタティック方式で一6KVの電圧でコロナ帯電し
、暗所に10秒間保持した後、タングステンランプを光
源として試料面照度が5.0ルクスになるように露光し
、電子写真特性の評価を行い次の結果が得られた。
The photosensitive plate produced in this way was left in an atmosphere of 25°C and 55% RH (relative humidity) to control the humidity, and then tested using an electrostatic paper tester (Kawaguchi Electric Seisakusho "5P-428J"). After corona charging with a static method at a voltage of -6 KV and holding in a dark place for 10 seconds, the sample was exposed to light using a tungsten lamp as a light source so that the sample surface illuminance was 5.0 lux, and the electrophotographic characteristics were evaluated. The results were obtained.

Vo(帯電の初期電圧)=−780(V)V d 10
 (暗所での10秒間の電位保持率)=82.0(%) E34(半減衰露光量) =2.0 (ルクス・秒)文
崖1」 例示化合物2)を用いたほかは、実施例1と同様にして
特性を測定したところ、結果はつぎのとおりであった。
Vo (initial charging voltage) = -780 (V) V d 10
(Potential retention rate for 10 seconds in the dark) = 82.0 (%) E34 (Half-attenuation exposure amount) = 2.0 (Lux seconds) Bungai 1" Exemplary compound 2) was used. The properties were measured in the same manner as in Example 1, and the results were as follows.

Vo=−610(V) VdlO=71 、5 (%) E3A=3.1(ルクス・秒) 支凰舊J 例示化合物3)1゜5部とポリエステル樹脂(東洋紡「
バイロン200J)1部とを、1.2−ジクロルエタン
250部中に入れてボールミルで分散させ、分散液をア
ルミニウム蒸着させたポリエステルフィルム上に塗布し
、120℃の熱風で30分間乾燥して、膜厚0.5部m
のキャリア発生層を設けた。
Vo = -610 (V) VdlO = 71,5 (%) E3A = 3.1 (lux seconds) Shikoji J Exemplary compound 3) 1°5 parts and polyester resin (Toyobo "
1 part of Vylon 200J) was placed in 250 parts of 1,2-dichloroethane and dispersed in a ball mill.The dispersion was applied onto a polyester film coated with aluminum and dried with hot air at 120°C for 30 minutes to form a film. Thickness 0.5 part m
A carrier generation layer was provided.

その上に、9−エチルカルバゾール−3−カルボアルデ
ヒド−1,1−ジフェニルヒドラ7710部とポリエス
テル樹脂(#記「バイロン200J)10部とを1.2
−ジクロルエタン100部に溶解した溶液を塗布し、6
0℃の温風で3時間乾燥して膜厚15gmのキャリア輸
送層を形成した。
On top of that, 7710 parts of 9-ethylcarbazole-3-carbaldehyde-1,1-diphenylhydra and 10 parts of polyester resin (marked with # "Vylon 200J)" were added at 1.2 parts.
- Apply a solution dissolved in 100 parts of dichloroethane, and
It was dried with warm air at 0° C. for 3 hours to form a carrier transport layer with a thickness of 15 gm.

この電子写真感光体の特性を測定して次の結果を得た。The characteristics of this electrophotographic photoreceptor were measured and the following results were obtained.

V o = −840(V) VdlO=87.0(%) E局=3.1(ルクスφ秒) 支立血1:ユ」 実施例3における例示化合物3)に代えて下記の例示化
合物を使用し、そのほかは実施例3と同様にして感光体
を製造した。
V o = -840 (V) VdlO = 87.0 (%) E station = 3.1 (lux φ seconds) Support blood 1: Yu'' In place of exemplified compound 3) in Example 3, the following exemplified compound was used. A photoreceptor was manufactured in the same manner as in Example 3 except for the following.

それぞれの特性な下記の通りである。The characteristics of each are as follows.

4    4)    −93083,51,85B)
     −65078,02,2137)     
−59091,52,779)     −81078
,51,9812)    −74085,03,29
14)     −filo    94.0   2
.810     15)     −88085,5
3,11119)     −75081,52,8丈
11LLヱ 実施例1で製造した電子写真感光体の帯電−放電を1,
000回繰り返し、特性の変化をしらべた。結果は次の
通りであり、繰り返し安定性が優れていることがわかっ
た。
4 4) -93083,51,85B)
-65078,02,2137)
-59091,52,779) -81078
,51,9812) -74085,03,29
14) -filo 94.0 2
.. 810 15) -88085,5
3,11119) -75081,52,8 length 11LLヱThe charging and discharging of the electrophotographic photoreceptor manufactured in Example 1 was 1,
The test was repeated 000 times to examine changes in characteristics. The results are as follows, and it was found that the repeated stability was excellent.

100回目  t、ooo回目 V o (V)     −790−790V d 1
0 (%)     81.0     81.5E%
(ルクス・秒)   2.1     2.2実[ アルミ貼り合わせポリエステルフィルム(アルミ箔の膜
厚toILm)上に、塩化ビニル−酢酸ビニル−無水マ
レイン酸共重合体(M水化学「エスレックMF−10」
)からなる厚さ0.021Lmの中間層を設け、−その
上に例示化合物2)1部を1.4−ジオキサン50部中
にアトライターで分散させた分散液を塗布し、100℃
の熱風で30分間乾燥して膜厚0.2部mのキャリア発
生層を設けた。
100th time t, oooth time V o (V) -790-790V d 1
0 (%) 81.0 81.5E%
(Lux/sec) 2.1 2.2 Actual [Vinyl chloride-vinyl acetate-maleic anhydride copolymer (M Water Chemical "S-LEC MF-10 ”
) with a thickness of 0.021 Lm was provided, and a dispersion of 1 part of exemplified compound 2) dispersed in 50 parts of 1,4-dioxane using an attritor was applied thereon, and the mixture was heated at 100°C.
After drying with hot air for 30 minutes, a carrier generation layer having a thickness of 0.2 part m was provided.

その上に2.5−ビス(4−N、N−ジエチルアミノフ
ェニル)−1,3,4−オキサジアゾール6部とポリカ
ーボネート樹脂(三蓉ガス化学「コーピロン5=100
0J)10部とを1.2−ジクロルエタン100部中に
溶解した溶液を塗布し、60℃の温風で3時間乾燥して
、膜厚104mのキャリア発生層を形成した。
On top of that, 6 parts of 2,5-bis(4-N,N-diethylaminophenyl)-1,3,4-oxadiazole and a polycarbonate resin (Sanyo Gas Chemical Co., Ltd. "Corpilon 5 = 100
A solution prepared by dissolving 10 parts of 0J) in 100 parts of 1,2-dichloroethane was applied and dried with warm air at 60°C for 3 hours to form a carrier generation layer with a thickness of 104 m.

こうして得た電子写真感光体のE34を測定したところ
、3.0ルクス・秒であった。この電子写真感光体を暗
所で一7KVのコロナ放電により帯電させ、最大光量3
0ルクス・秒で像露光した後、磁気ブラシ法により現像
し、ついて転写を行ったところ、コント5ストが充分で
階調性のよい鮮明な画像が選られた。
When the E34 of the electrophotographic photoreceptor thus obtained was measured, it was 3.0 lux·sec. This electrophotographic photoreceptor was charged with a corona discharge of 17 KV in a dark place, and the maximum amount of light was 3.
After imagewise exposure at 0 lux/second, development was performed using a magnetic brush method, and subsequent transfer was performed, resulting in a clear image with sufficient contrast and good gradation.

Claims (2)

【特許請求の範囲】[Claims] (1)導電性支持体に上に下記の一般式( I )で示さ
れるトリスアゾ化合物を含有する感光層を設けたことを
特徴とする電子写真感光体。 ▲数式、化学式、表等があります▼( I ) (但し、上記式中Aは、一般式 ▲数式、化学式、表等があります▼ で表わされ、上記式においてRは水素原子、置換または
非置換のアルキル基、芳香族炭化水素基あるいは芳香族
複素環基を表わす。)
(1) An electrophotographic photoreceptor characterized in that a photosensitive layer containing a trisazo compound represented by the following general formula (I) is provided on a conductive support. ▲There are mathematical formulas, chemical formulas, tables, etc.▼(I) (However, A in the above formula is represented by the general formula ▲There are mathematical formulas, chemical formulas, tables, etc.▼, and in the above formula, R is a hydrogen atom, substituted or unsubstituted. (Represents a substituted alkyl group, aromatic hydrocarbon group, or aromatic heterocyclic group.)
(2)感光層がキャリア発生物質とキヤリヤー輸送物質
を含有し、この感光層が上記一般式( I )で示される
トリスアゾ化合物である特許請求の範囲第(1)項に記
載の電子写真感光体。
(2) The electrophotographic photoreceptor according to claim (1), wherein the photosensitive layer contains a carrier-generating substance and a carrier-transporting substance, and the photosensitive layer is a trisazo compound represented by the above general formula (I). .
JP3276186A 1986-02-19 1986-02-19 Electrophotographic sensitive body Granted JPS62192750A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3276186A JPS62192750A (en) 1986-02-19 1986-02-19 Electrophotographic sensitive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3276186A JPS62192750A (en) 1986-02-19 1986-02-19 Electrophotographic sensitive body

Publications (2)

Publication Number Publication Date
JPS62192750A true JPS62192750A (en) 1987-08-24
JPH0469951B2 JPH0469951B2 (en) 1992-11-09

Family

ID=12367823

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3276186A Granted JPS62192750A (en) 1986-02-19 1986-02-19 Electrophotographic sensitive body

Country Status (1)

Country Link
JP (1) JPS62192750A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0441975U (en) * 1990-07-31 1992-04-09
EP1367449A3 (en) * 2002-05-31 2005-01-05 Samsung Electronics Co., Ltd. Organophotoreceptor with a UV-light stabilizer

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53132347A (en) * 1977-04-25 1978-11-18 Ricoh Co Ltd Photoreceptor for electrophotography
JPS54109438A (en) * 1978-02-15 1979-08-28 Ricoh Co Ltd Photosensitive material for zerography
JPS57203062A (en) * 1981-06-10 1982-12-13 Ricoh Co Ltd Novel triazo compound and its preparation
JPS57206658A (en) * 1981-06-12 1982-12-18 Ricoh Co Ltd Novel trisazo compound and its preparation
JPS5831341A (en) * 1981-08-19 1983-02-24 Canon Inc Electrophotographic receptor
JPS59196366A (en) * 1983-04-21 1984-11-07 Ricoh Co Ltd Novel trisazo compound and production thereof
JPS6111754A (en) * 1984-06-27 1986-01-20 Mitsubishi Paper Mills Ltd Electrophotographic sensitive body
JPS6122346A (en) * 1984-07-10 1986-01-30 Mitsubishi Paper Mills Ltd Electrophotographic sensitive body

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53132347A (en) * 1977-04-25 1978-11-18 Ricoh Co Ltd Photoreceptor for electrophotography
JPS54109438A (en) * 1978-02-15 1979-08-28 Ricoh Co Ltd Photosensitive material for zerography
JPS57203062A (en) * 1981-06-10 1982-12-13 Ricoh Co Ltd Novel triazo compound and its preparation
JPS57206658A (en) * 1981-06-12 1982-12-18 Ricoh Co Ltd Novel trisazo compound and its preparation
JPS5831341A (en) * 1981-08-19 1983-02-24 Canon Inc Electrophotographic receptor
JPS59196366A (en) * 1983-04-21 1984-11-07 Ricoh Co Ltd Novel trisazo compound and production thereof
JPS6111754A (en) * 1984-06-27 1986-01-20 Mitsubishi Paper Mills Ltd Electrophotographic sensitive body
JPS6122346A (en) * 1984-07-10 1986-01-30 Mitsubishi Paper Mills Ltd Electrophotographic sensitive body

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0441975U (en) * 1990-07-31 1992-04-09
EP1367449A3 (en) * 2002-05-31 2005-01-05 Samsung Electronics Co., Ltd. Organophotoreceptor with a UV-light stabilizer

Also Published As

Publication number Publication date
JPH0469951B2 (en) 1992-11-09

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