JPH0264550A - Electrophotographic sensitive body - Google Patents

Electrophotographic sensitive body

Info

Publication number
JPH0264550A
JPH0264550A JP21691188A JP21691188A JPH0264550A JP H0264550 A JPH0264550 A JP H0264550A JP 21691188 A JP21691188 A JP 21691188A JP 21691188 A JP21691188 A JP 21691188A JP H0264550 A JPH0264550 A JP H0264550A
Authority
JP
Japan
Prior art keywords
formula
charge transport
photoreceptor
layer
formulas
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
JP21691188A
Other languages
Japanese (ja)
Other versions
JP2683054B2 (en
Inventor
Masaaki Ko
弘 正明
Youichi Kawamorita
陽一 川守田
Akira Yoshida
晃 吉田
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 JP63216911A priority Critical patent/JP2683054B2/en
Publication of JPH0264550A publication Critical patent/JPH0264550A/en
Application granted granted Critical
Publication of JP2683054B2 publication Critical patent/JP2683054B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • G03G5/05Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0503Inert supplements
    • G03G5/051Organic non-macromolecular compounds
    • G03G5/0517Organic non-macromolecular compounds comprising one or more cyclic groups consisting of carbon-atoms only
    • 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
    • G03G5/05Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
    • G03G5/0503Inert supplements
    • G03G5/051Organic non-macromolecular compounds
    • G03G5/0521Organic non-macromolecular compounds comprising one or more heterocyclic groups

Landscapes

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

Abstract

PURPOSE:To improve the durability or the subject body at corona discharge environments and to always make a picture high quality by incorporating a prescribed charge transfer substance and two kinds of specified additives in the photosensitive body. CONSTITUTION:The charge transfer substance (such as a hydrazone compd.) having an oxidation potential of <0.6V and the additives shown by formulas I and II are incorporated in the surface layer of the photosensitive body. In formula I, X1 is t-Bu or t-Am, X2 is hydrogen atom or 2-10 C alkenyl, etc. In formula III, R is halogen or hydrogen atom, X1 and X2 are each 1-10 C alkyl or 2-10 C alkenyl. The additives shown by formula I is composed of a compd. shown by formula II, etc. The additives shown by formula III is composed of a compd. shown by formula IV, etc. Further the surface layer preferably contains lubricating powders such as fluorine resin powders (for example, polytetra fluoroethylene powders), etc.

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、さらに詳しくは、繰り
返しによる画質劣化のない耐久性に優れた感光層を有す
る電子写真感光体に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an electrophotographic photoreceptor, and more particularly, to an electrophotographic photoreceptor having a photosensitive layer with excellent durability and no deterioration in image quality due to repeated use.

〔従来の技術〕[Conventional technology]

近年、有機化合物を光導電体として用いた電子写真感光
体が数多く開発されている。その中で実用化されている
ものは、はとんどが光導電体を電荷発生物質と電荷輸送
物質とに機能分離した形態をとっている。
In recent years, many electrophotographic photoreceptors using organic compounds as photoconductors have been developed. Most of those that have been put to practical use have a form in which the photoconductor is functionally separated into a charge-generating material and a charge-transporting material.

このような有機光導電体を用いた電子写真感光体は、材
料設計の柔軟性から感度、光応答性などの電子写真特性
のさらなる向上が期待され、また成膜性が容易で生産性
が高いことが特徴とされている。
Electrophotographic photoreceptors using such organic photoconductors are expected to further improve electrophotographic properties such as sensitivity and photoresponsiveness due to the flexibility of material design, and are easy to form into films and have high productivity. It is characterized by this.

しかしながら、これらの感光体は一般的に耐久性が低い
ことが大きな欠点であるとされてきた。
However, it has been said that a major drawback of these photoreceptors is that they generally have low durability.

耐久性としては感度、残留電位、帯電能、画像ボケなど
の電子写真物性面の耐久性、及び摺擦による感光体表面
の摩耗や傷などの機械的耐久性に大別されるが、電子写
真物性面の耐久性に関してはコロナ帯電器から発生する
オゾン、NOx等により感光体表面層に含有される電荷
輸送物質が劣化することが原因であることが知られてい
る。
Durability can be roughly divided into durability of electrophotographic physical properties such as sensitivity, residual potential, charging ability, and image blur, and mechanical durability such as abrasion and scratches on the photoreceptor surface due to rubbing. It is known that the durability of the physical properties is caused by the deterioration of the charge transport material contained in the surface layer of the photoreceptor due to ozone, NOx, etc. generated from the corona charger.

特に電荷輸送物質の酸化電位が0.6V未満のときは、
この劣化は著しく、耐久につれて画像がつぶれ、文字が
判別できない、いわゆる画像ボケという現象が顕著にお
きてくるものであった。従って、高品位の画像を得るた
めには感光体表面を研摩して常にフレッシュな面を出す
ことが不可欠であった。しかしながら、感光体表面に各
種滑材を分散させる等機械的耐久性の向上がはかられる
に伴ない、削れ量が著しく減少し、劣化した電荷輸送物
質の除去がすみやかに行われなくなり画像ボケの発生が
顕在化しているのが現状であった。
Especially when the oxidation potential of the charge transport substance is less than 0.6V,
This deterioration was significant, and over time the image became distorted and characters became indistinguishable, a phenomenon known as image blurring. Therefore, in order to obtain high-quality images, it is essential to polish the surface of the photoreceptor to always present a fresh surface. However, as efforts have been made to improve mechanical durability by dispersing various lubricants on the surface of the photoreceptor, the amount of abrasion has decreased significantly, and deteriorated charge transport materials cannot be removed quickly, resulting in blurred images. The current situation is that the outbreak is becoming more obvious.

我々はこれらの問題の解決策として特開昭63−308
50号公報に示したように表面層に含まれる電荷輸送物
質として酸化電位が0.6V以上の化合物を用いること
が有効であることを見い出し、高耐久性感光体を実用化
してきたが、その感光体の使われ方によっては新たな問
題点が指摘されてきた。即ち、感光体を連続して使用し
た後、長期間複写機内に放置すると、コロナ放電を行う
帯電器に近接した感光体の部位の帯電能が見掛は上低下
した現象がおこり、画像上に白スジが発生する現象、い
わゆる白ヌケが現われることである。この白ヌケ現象は
酸化電位が0.6V以上の電荷輸送物質を用いた際の特
有な現象であり、0.6V未満の低酸化電位の電荷輸送
物質には全く見られないものである。前述の画像ボケと
白ヌケの発生はコロナ放電時に発生したオゾンやNOx
に起因するものであり、電荷輸送物質の酸化電位が0.
6V未満の場合には電荷輸送物質自身が感光体表面でオ
ゾンやNOxの作用で酸化を受けて低抵抗化し画像ボケ
が生起するのに対し、酸化電位が0.6V以上の電荷輸
送物質においてはそれ自身が酸化作用を受けにくいため
にオゾンやNOxが感光体深層部まで浸透して電荷発生
物質を酸化、低抵抗化するために基体からのホール注入
が促進され、見掛は上電位がのらずに白ヌケ現象が生起
するものと推定される。この見掛は上の電位低下は耐久
途中でも生起しているものであるが、表面電位の低下が
感光体表面で均一におこるために部分的な電位低下であ
る白ヌケ現象とは観測されず、連続使用後に放置した際
に、オゾンやNOx flJ度が極端に高い帯電器近傍
での局部的な電位低下が白ヌケとなって顕著に表面化す
るものである。
As a solution to these problems, we have proposed
As shown in Publication No. 50, it was discovered that it is effective to use a compound with an oxidation potential of 0.6 V or more as a charge transport substance contained in the surface layer, and a highly durable photoreceptor has been put into practical use. New problems have been pointed out depending on how photoreceptors are used. In other words, if a photoreceptor is left in a copying machine for a long period of time after being used continuously, a phenomenon occurs in which the charging ability of the portion of the photoreceptor close to the charger that performs corona discharge is apparently reduced, and the image is This is the appearance of white streaks, so-called white spots. This white-out phenomenon is a peculiar phenomenon when a charge transport material having an oxidation potential of 0.6V or more is used, and is not observed at all in a charge transport material having a low oxidation potential of less than 0.6V. The above-mentioned image blur and white spots are caused by ozone and NOx generated during corona discharge.
This is due to the fact that the oxidation potential of the charge transport substance is 0.
When the oxidation potential is less than 6V, the charge transport material itself is oxidized by the action of ozone and NOx on the surface of the photoreceptor, resulting in lower resistance and image blurring. Since ozone and NOx themselves are not susceptible to oxidation, ozone and NOx penetrate deep into the photoreceptor, oxidize the charge-generating material, and lower the resistance, promoting hole injection from the substrate, and the apparent upper potential increases. It is presumed that the white spot phenomenon occurs without any problems. This apparent drop in potential occurs even during the durability test, but because the drop in surface potential occurs uniformly on the surface of the photoreceptor, it is not observed as a white spot phenomenon, which is a partial drop in potential. When the battery is left after continuous use, a local potential drop near the charger where ozone and NOx flJ levels are extremely high becomes noticeable as white spots.

〔本発明が解決しようとする問題点〕[Problems to be solved by the present invention]

本発明は前述の問題点を解決した電子写真感光体を提供
するものである。即ち本発明の目的は画像ボケや白ヌケ
の発生しない高品位の画像が得られる電子写真感光体を
提供するものである。
The present invention provides an electrophotographic photoreceptor that solves the above-mentioned problems. That is, an object of the present invention is to provide an electrophotographic photoreceptor capable of producing high-quality images without image blur or white spots.

本発明の他の目的は摺擦による表面の摩耗やキズの発生
が少なく、かつ画像ボケや白ヌケの発生しない高品位の
画像が得られる高耐久性を有する電子写真感光体を提供
するものである。更に本発明の他の目的は、くり返し電
子写真プロセスにおいて残留電位の蓄積がなく、常に高
品位の画像が得られる電子写真感光体を提供するもので
ある。
Another object of the present invention is to provide an electrophotographic photoreceptor with high durability, which has less surface wear and scratches caused by rubbing, and which can produce high-quality images without blurring or white spots. be. Still another object of the present invention is to provide an electrophotographic photoreceptor that does not accumulate residual potential during repeated electrophotographic processes and can always produce high-quality images.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者らはかかる目的に従って鋭意検討を重ねた結果
、酸化電位が0.6V未満の電荷輸送物質を用いる感光
体においても特定の構造を有する有機化合物を少なくと
も2種類添加することによりその劣化を防止し、画像ボ
ケの生じない感光体を得ることが可能であることを見い
出し本発明を完成した。すなわち本発明は導電性基体上
に感光層を有する電子写真感光体において、表面層が酸
化電位0.6V未満の電荷輸送物質と、°下記一般式(
1)および(2)で表わされる化合物を含有することを
特徴とする電子写真感光体である。
The inventors of the present invention have made extensive studies in accordance with the above objective, and have found that even in photoreceptors that use charge transport materials with an oxidation potential of less than 0.6V, the deterioration can be prevented by adding at least two types of organic compounds having specific structures. The present invention has been completed based on the discovery that it is possible to prevent the occurrence of image blurring and to obtain a photoreceptor without image blurring. That is, the present invention provides an electrophotographic photoreceptor having a photosensitive layer on a conductive substrate, in which the surface layer contains a charge transporting material having an oxidation potential of less than 0.6 V, and the following general formula (
This is an electrophotographic photoreceptor characterized by containing the compounds represented by (1) and (2).

一般式(1)および(2)の化合物の添加効果は、電荷
輸送物質をオゾンやNOxの酸化作用から保護すること
にある。即ち、一般式(1)および(2)の化合物は電
荷輸送物質より優先的にオゾンやNOxの酸化作用をう
けるものであり、その酸化劣化物が他の電子写真特性へ
の弊害のないことを見い出し本発明を完成するにいたっ
たものである。特に本発明の特徴は単独ではその添加効
果が小さい化合物の両者を併用することによって初めて
最良の結果が得られることを見い出したことである。
The effect of adding the compounds of general formulas (1) and (2) is to protect the charge transport material from the oxidizing effects of ozone and NOx. That is, the compounds of general formulas (1) and (2) are preferentially oxidized by ozone and NOx over charge transport substances, and it is confirmed that the oxidized deterioration products do not have any adverse effects on other electrophotographic properties. Heading This is what led to the completion of the present invention. In particular, the present invention is characterized by the discovery that the best results can only be obtained by using both compounds, which have little effect when added alone.

又、本発明の電子写真感光体は電荷輸送物質の劣化がな
いため、各種滑材粉体の添加による高耐久化(耐久によ
る表面層の削れ量減少)への適用も十分に可能なもので
ある。
In addition, since the electrophotographic photoreceptor of the present invention has no deterioration of the charge transporting substance, it is fully applicable to increasing durability (reducing the amount of abrasion of the surface layer due to durability) by adding various lubricant powders. be.

以下本発明の詳細な説明する。The present invention will be explained in detail below.

本発明における感光層は、機能分離された電荷発生物質
と電荷輸送物質とが混合された単層型感光体、あるいは
電荷発生物質を含む電荷発生層と、電荷輸送物質を含む
電荷輸送層を積層した積層型感光体などの形態をとる。
The photosensitive layer in the present invention is a single-layer type photoreceptor in which a functionally separated charge generating substance and a charge transporting substance are mixed, or a stacked layer of a charge generating layer containing a charge generating substance and a charge transporting layer containing a charge transporting substance. It takes the form of a laminated photoreceptor.

電荷発生物質としては、ピリリウム、チオピリリウム系
染料、フタロシアニン系顔料、アントアントロン顔料、
ペリレン顔料、ジベンズピレンキノン顔料、ピラントロ
ン顔料、アゾ顔料、インジゴ顔料、キナクリドン系顔料
などの有機光導電体が用いられる。
Examples of charge-generating substances include pyrylium, thiopyrylium dyes, phthalocyanine pigments, anthoanthrone pigments,
Organic photoconductors such as perylene pigments, dibenzpyrenequinone pigments, pyranthrone pigments, azo pigments, indigo pigments, and quinacridone pigments are used.

酸化電位0.6v未満の電荷輸送物質としては、ピラゾ
リン系、ヒドラゾン系、スチルベン系、トリアリールメ
タン系、オキサゾール系、チアゾール系、カルバソール
系化合物、ボリアリールアルカン類などの有機光導電体
から選択される。
The charge transport substance with an oxidation potential of less than 0.6 V is selected from organic photoconductors such as pyrazoline, hydrazone, stilbene, triarylmethane, oxazole, thiazole, carbazole, and polyarylalkane compounds. Ru.

単層型感光体の場合は上記の電荷発生物質と電荷輸送物
質を適当な結着樹脂に溶解または分散し、塗布により導
電性基体上に層を形成する。一方、積層型としては、導
電性基体上に1)電荷発生層、電荷輸送層の順に積層す
るもの、あるいは2)電荷輸送層、電荷発生層の順に積
層するものがある。1)の場合には電荷発生層の形成法
として、結着樹脂と溶剤中に電荷発生物、質を分散また
は溶解して塗布する方法や蒸着、スパッタリング等の方
法がある。膜厚は5μm以下、特には0.01〜3μm
が好ましい。なお、この場合には、セレン、アモルファ
スシリコンなどの無機光導電体を用いることもできる。
In the case of a single-layer type photoreceptor, the charge-generating substance and charge-transporting substance described above are dissolved or dispersed in a suitable binder resin, and a layer is formed on the conductive substrate by coating. On the other hand, the laminated type includes one in which 1) a charge generation layer and a charge transport layer are laminated in this order on a conductive substrate, and 2) a type in which a charge transport layer and a charge generation layer are laminated in that order. In the case of 1), methods for forming the charge generating layer include a method of dispersing or dissolving a charge generating substance in a binder resin and a solvent and coating the mixture, and a method of vapor deposition, sputtering, and the like. The film thickness is 5 μm or less, especially 0.01 to 3 μm
is preferred. In this case, an inorganic photoconductor such as selenium or amorphous silicon can also be used.

電荷輸送層は上述の電荷輸送物質を成膜性のある結着樹
脂中に溶解して電荷発生層上に積層する。膜厚は5〜4
0μm1特には8〜35μmが好ましい。本発明の化合
物は、この場合、電荷輸送層に含有される。
The charge transport layer is formed by dissolving the charge transport material described above in a binder resin having film-forming properties and laminating it on the charge generation layer. Film thickness is 5-4
0 μm1, particularly preferably 8 to 35 μm. The compound of the invention is in this case contained in the charge transport layer.

一方、電荷輸送層上に電荷発生層を積層する場合は、ど
ちらの層も上述の有機光導電体を結着樹脂と共に塗布す
ることにより層を形成することができる。この時、電荷
発生層中には電荷輸送物質を含有させる。この場合には
化合物は電荷発生層もしくは電荷発生層と電荷輸送層の
両者に含有させる。
On the other hand, when a charge generation layer is laminated on the charge transport layer, both layers can be formed by applying the above-mentioned organic photoconductor together with a binder resin. At this time, a charge transport material is contained in the charge generation layer. In this case, the compound is contained in the charge generation layer or both the charge generation layer and the charge transport layer.

以下に、本発明に用いる一般式(1)および(2)の化
合物の具体例を示す。
Specific examples of the compounds of general formulas (1) and (2) used in the present invention are shown below.

また、本発明で用いることができる滑材粉体は、フッ素
系樹脂粉体、ポリオレフィン系粉体およびフッ化カーボ
ン粉体等から選ばれる。滑材および離型性の点からフッ
素光樹脂粉゛体が好ましい。フッ素系樹脂粉体としては
、四フッ化エチレン樹脂、三フッ化塩化エチレン樹脂、
四フッ化エチレンー六フッ化プロピレン樹脂、フッ化ビ
ニル樹脂、フッ化ビニリデン樹脂、ニフツ化塩化エチレ
ンおよびそれらの共重合体等が、ポリオレフィン系粉体
としては、ポリエチレン、ポリプロピレン、およびそれ
らの共重合体等を用いることができ、これら滑材粉体の
添加量はバインダーに対して1〜lOO重量%が適当で
あり、特に1.5〜30重量%が好ましい。
Furthermore, the lubricant powder that can be used in the present invention is selected from fluororesin powder, polyolefin powder, fluorocarbon powder, and the like. Fluoropolymer powder is preferred from the viewpoint of lubricant and mold release properties. Fluorine resin powders include tetrafluoroethylene resin, trifluorochloroethylene resin,
Examples of polyolefin powder include polyethylene, polypropylene, and copolymers thereof. The amount of these lubricant powders added is suitably 1 to 100% by weight, particularly preferably 1.5 to 30% by weight, based on the binder.

本発明で用いる前記化合物(1)および(2)の添加量
はその和で表面層の重量分率で0.2〜20wt%、好
ましくは0.6〜15wt%の範囲が好ましい。
The added amount of the compounds (1) and (2) used in the present invention is preferably in the range of 0.2 to 20 wt%, preferably 0.6 to 15 wt% in terms of the weight fraction of the surface layer.

添加量が0.2wt%未満では劣化防止効果が小さく2
0wt%を超えると感度低下、残留電位の上昇等弊害が
生ずる。
If the amount added is less than 0.2 wt%, the deterioration prevention effect is small2.
If it exceeds 0 wt%, adverse effects such as a decrease in sensitivity and an increase in residual potential will occur.

本発明の電子写真感光体を製造する場合、基体としては
、基体自体が導電性をもつもの、例えばアルミニウム、
アルミニウム合金、ステンレス等の金属や合金を用いる
ことができ、その他にアルミニウム、アルミニウム合金
、酸化インジウム、酸化錫、酸化インジウム−酸化錫合
金等を真空蒸着法によって被膜形成した層を有するプラ
スチック、導電性粒子を適当なバインダーとともにプラ
スチックや金属あるいは合金の上に被覆した基体、導電
性粒子をプラスチックや紙に含浸した基体や導電性ポリ
マーを有するプラスチック等を用いることができる。
When manufacturing the electrophotographic photoreceptor of the present invention, the substrate itself is conductive, such as aluminum,
Metals and alloys such as aluminum alloys and stainless steel can be used, and in addition, plastics and conductive materials have layers formed by vacuum deposition of aluminum, aluminum alloys, indium oxide, tin oxide, indium oxide-tin oxide alloys, etc. A substrate in which particles are coated on plastic, metal, or an alloy together with a suitable binder, a substrate in which plastic or paper is impregnated with conductive particles, a plastic containing a conductive polymer, etc. can be used.

導電基体と感光層の中間に、バリヤー機能と接着機能を
もつ下引層を設けることもできる。下引層は、カゼイン
、ポリビニルアルコール、ニトロセルロール、エチレン
−アクリル酸コポリマー、ポリビニルブチラール、フェ
ノール樹脂、ポリアミド、ポリウレタン、ゼラチン、酸
化アルミニウムなどによって形成できる。
A subbing layer having barrier and adhesive functions can also be provided between the conductive substrate and the photosensitive layer. The subbing layer can be formed from casein, polyvinyl alcohol, nitrocellulose, ethylene-acrylic acid copolymer, polyvinyl butyral, phenolic resin, polyamide, polyurethane, gelatin, aluminum oxide, and the like.

下引層の膜厚は、01μm〜40μm1好ましくは、0
.3μm〜3μmが適当である。
The thickness of the subbing layer is 01 μm to 40 μm1, preferably 0
.. 3 μm to 3 μm is suitable.

滑材粉体の分散法としては、一般的な分散手段、即ち、
ホモジナイザー、超音波、ボールミル、振動ボールミル
、サンドミル、アトライター、ロールミルなどを用いる
ことができる。適当な溶剤に溶解したバインダーに滑材
粉体を加えた後上記分散法により分散する。これをバイ
ンダーと電界輸送物質及び一般式(1)および(2)の
化合物を溶解した溶液に適量混合するこよにより調製す
る。
As a method for dispersing lubricant powder, general dispersion means are used, namely,
A homogenizer, an ultrasonic wave, a ball mill, a vibrating ball mill, a sand mill, an attriter, a roll mill, etc. can be used. The lubricant powder is added to the binder dissolved in a suitable solvent, and then dispersed by the above-mentioned dispersion method. This is prepared by mixing an appropriate amount with a solution in which the binder, the electrotransport material, and the compounds of general formulas (1) and (2) are dissolved.

又、滑材粉体を分散させる際に分散性を向上させるため
に各種の分散助剤を添加することも可能である。
Furthermore, various dispersion aids can be added to improve the dispersibility when dispersing the lubricant powder.

塗工は、浸漬コーティング法、スプレーコーティング法
、マイヤーバーコーティング法、ブレードコーティング
法等のコーティング法を用いて行うことができる。乾燥
は、室温における指触乾燥後、加熱乾燥する方法が好ま
しい。加熱乾燥は、30℃〜200℃で5分〜2時間の
範囲の時間で静止または送風下で行うことができる。
Coating can be performed using a coating method such as a dip coating method, a spray coating method, a Meyer bar coating method, or a blade coating method. For drying, it is preferable to dry to the touch at room temperature and then heat dry. Heat drying can be carried out at 30° C. to 200° C. for a period of 5 minutes to 2 hours, either stationary or with ventilation.

本発明における酸化電位は、飽和カロメル電極を参照電
極、O,lN (n−Bu)4N”1RCI! 04−
アセトニトリル溶液を電界液として用い、ポテンシャル
スィーパ−によって作用電極の電位をスィーブし、得ら
れた電流−電位曲線のピーク位置をそのまま酸化電位の
値として求めた。すなわちまず、試料を、0.IN (
n−Bu)4N”CI O4−アセトニトリル溶液の電
界液に5〜10 m mo1%になるように溶かす。そ
してこの試料溶液に、電圧を印加し低電位から直線的に
電圧を変化させ、電流の変化を測定して電流−電位曲線
を求める。この電流−電位曲線における電流値の最初の
変曲点に対応した電位値を本発明の酸化電位とした。
The oxidation potential in the present invention is determined using a saturated calomel electrode as a reference electrode, O, IN (n-Bu)4N"1RCI! 04-
Using an acetonitrile solution as an electrolyte, the potential of the working electrode was swept with a potential sweeper, and the peak position of the obtained current-potential curve was directly determined as the value of the oxidation potential. That is, first, the sample was heated to 0. IN (
n-Bu)4N"CI O4-acetonitrile solution in an electrolytic solution to a concentration of 5 to 10 mmol1%. Then, a voltage is applied to this sample solution and the voltage is changed linearly from a low potential to increase the current. The change was measured to obtain a current-potential curve.The potential value corresponding to the first inflection point of the current value in this current-potential curve was defined as the oxidation potential of the present invention.

本発明の電子写真感光体は、通常の複写機の他、レーザ
ービームプリンター、LEDプリンター、LCDプリン
ター、CRTプリンターなど電子写真方法を応用した種
々の機器の感光体に適用できる。
The electrophotographic photoreceptor of the present invention can be applied to photoreceptors of various devices to which electrophotography is applied, such as ordinary copying machines, laser beam printers, LED printers, LCD printers, and CRT printers.

以下、実施例にて本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1 基体として80φX360mmのアルミニウムシリンダ
ーを用意した。
Example 1 An aluminum cylinder of 80φ x 360mm was prepared as a base.

一方、酸化アンチモン10%を含有する酸化スズを酸化
チタンに対して75重量%になるように被覆した導電性
粉体100部(重量部、以下同様)をレゾール系フェノ
ール樹脂100部笈びメタノール30部、メチルセロソ
ルブ100部より成る溶液に加え、ボールミル装置でよ
(分散し塗料とした。この塗料を基体上に浸漬塗布し1
40℃で30分間加熱硬化させ、20μmの導電層をも
うけた。
On the other hand, 100 parts (parts by weight, the same shall apply hereinafter) of conductive powder coated with tin oxide containing 10% antimony oxide at a concentration of 75% by weight relative to titanium oxide were mixed with 100 parts of resol-based phenolic resin and 30 parts methanol. 100 parts of methyl cellosolve and dispersed in a ball mill to form a paint. This paint was applied by dip coating onto a substrate.
It was heated and cured at 40° C. for 30 minutes to form a 20 μm conductive layer.

この上にポリアミド樹脂(6−66−610−124元
ナイロン共重合体)1部および8−ナイロン樹脂(メト
キシメチル化6ナイロン、メトキシ化率的30%)3部
をメタノール50部ブタノール40部から成る溶剤に溶
解させた塗液を浸漬法で塗布し、70℃、10分間乾燥
後、0.5μm厚の下引き層をもうけた。
On top of this, 1 part of polyamide resin (6-66-610-124 nylon copolymer) and 3 parts of 8-nylon resin (methoxymethylated 6 nylon, methoxylation rate 30%) were added from 50 parts of methanol and 40 parts of butanol. A coating liquid dissolved in a solvent was applied by dipping, and after drying at 70°C for 10 minutes, a 0.5 μm thick undercoat layer was formed.

次に下記構造式(3) のビスアゾ顔料を10部、ポリビニルブチラール樹脂5
部、及びシクロへキサノン100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
液にテトラヒドロフラン50〜100 (適宜)部を加
えて下引き層上に塗布し、100’05分間の乾燥をし
て0.12μm厚の電荷発生層を形成した。
Next, 10 parts of bisazo pigment of the following structural formula (3) and 5 parts of polyvinyl butyral resin were added.
and 100 parts of cyclohexanone were dispersed for 20 hours using a sand mill device using 1φ glass beads. 50 to 100 (appropriate) parts of tetrahydrofuran were added to this dispersion and applied onto the undercoat layer, followed by drying for 100'05 minutes to form a charge generation layer with a thickness of 0.12 μm.

次に電荷輸送物質として下記構造式(4)のヒドラゾン
化合物〔酸化電位0.57V (略称CT−1))、下
記構造式(5)(THPM−1) 及び下記構造式(6)(BZT−1) の化合物、さらに結着剤バインダーとしてビスフェノー
ルA型ポリカーボネート樹脂を用意した。
Next, as charge transport materials, hydrazone compounds of the following structural formula (4) [oxidation potential 0.57 V (abbreviation CT-1)), the following structural formula (5) (THPM-1), and the following structural formula (6) (BZT- The compound 1) and a bisphenol A polycarbonate resin as a binding agent binder were prepared.

まずポリカーボネート樹脂20部と電荷輸送物質(4)
 20部及び添加剤として化合物(5)および(6)の
各々0.4部をモノクロルベンゼン100部に溶解し、
さらにジクロルエタン20部を加えて電荷輸送層塗布液
を作成した。この液を前記発生層上に塗布し100℃で
90分間熱風乾燥して20μm厚の電荷輸送層を形成し
た。
First, 20 parts of polycarbonate resin and charge transport material (4)
20 parts and 0.4 parts each of compounds (5) and (6) as additives were dissolved in 100 parts of monochlorobenzene,
Furthermore, 20 parts of dichloroethane was added to prepare a charge transport layer coating solution. This solution was applied onto the generation layer and dried with hot air at 100° C. for 90 minutes to form a charge transport layer with a thickness of 20 μm.

この感光体を現像器及びクリーナーユニットを取りはず
した複写機(改造キャノン製複写機NP−3525)に
搭載し、帯電露光プロセスを1万回繰り返し行った。そ
の後すぐに複写機(キャノン製NP−3525)にて−
コピーを行いコピー画像を目視により観察したが、画像
ボケは発生しておらず高品位の画像を得ることができた
This photoreceptor was mounted on a copying machine (modified Canon NP-3525 copying machine) from which the developer and cleaner unit had been removed, and the charging and exposure process was repeated 10,000 times. Immediately afterwards, using a copying machine (Canon NP-3525)
Copying was performed and the copied image was visually observed, but no image blurring occurred and a high-quality image could be obtained.

更に、この感光体について複写機(キャノン製NP−3
525)にて5000枚の画出し耐久を行い、そのまま
複写機内に3日間放置した後コピーを行った。その画像
は鮮明、高品位であり、放置中寄電器に近接した部分に
対応する位置にも白ヌケは認められなかった。
Furthermore, regarding this photoreceptor, a copying machine (Canon NP-3)
525) for printing 5,000 sheets, and after leaving it in a copying machine for 3 days, copies were made. The image was clear and of high quality, and no white spots were observed even in positions corresponding to areas close to the parasitic device during storage.

比較例1 実施例1において用いた添加剤を添加しない以外は実施
例1と同様に感光体を作成し、実施例1と同様の試験を
行った。その画像は画像全面に渡って画像ボケが発生し
文字の判別が不可能な状態であった。但し帯電器に近接
した部分に対応する位置の白ヌケは認められなかった。
Comparative Example 1 A photoreceptor was prepared in the same manner as in Example 1, except that the additives used in Example 1 were not added, and the same tests as in Example 1 were conducted. The image was blurred over the entire image, making it impossible to distinguish the characters. However, no white spots were observed at positions corresponding to areas close to the charger.

実施例2 電荷輸送物質として前記CT−1.酸化電位0.54V
の下記構造式(7)(略称CT−2)の化合物、又、特
性の構造を有する2種の添加剤として前記THPM−1
及びBZT−1の他に第1表に示す化合物を用い、実施
例1と同様にして作成した感光体について実施例1と同
様の評価を行った結果を第2表に示す。
Example 2 The above CT-1. Oxidation potential 0.54V
A compound of the following structural formula (7) (abbreviated as CT-2), and the above THPM-1 as two additives having a characteristic structure.
Table 2 shows the results of the same evaluations as in Example 1 for photoreceptors prepared in the same manner as in Example 1 using the compounds shown in Table 1 in addition to BZT-1.

及び酸化電位0.47Vの下記構造式(8)(略称CT
−3)の化合物 比較例2〜8 電荷輸送物質としてCT−2及びCT−3を用い本発明
の化合物を添加しないで実施例1と同様にして感光体を
作成、評価を行った。
and the following structural formula (8) (abbreviated as CT) with an oxidation potential of 0.47V
-3) Comparative Examples 2 to 8 of Compounds Photoreceptors were prepared and evaluated in the same manner as in Example 1 using CT-2 and CT-3 as charge transport materials and without adding the compound of the present invention.

また、電荷輸送物質としてCT−1を用い、化合物TH
PM−1またはBZT−1を1wt%添加した感光体を
実施例1と同様にしてそれぞれ作成、評価した。
In addition, using CT-1 as a charge transport material, compound TH
Photoreceptors containing 1 wt % of PM-1 or BZT-1 were prepared and evaluated in the same manner as in Example 1.

更に第3表に示す酸化電位0.6v以上の電荷輸送物質
を用いた感光体(添加剤なし)を実施例1と同様にして
作成、評価した。
Further, a photoreceptor (without additives) using a charge transport material having an oxidation potential of 0.6 V or higher shown in Table 3 was prepared and evaluated in the same manner as in Example 1.

第  3 表 結果を第4表にまとめて示す。Part 3 table The results are summarized in Table 4.

実施例22 実施例1で用いた電荷輸送物質、添加剤、ポリカーボネ
ート樹脂に加え、ポリ四フッ化エチレン樹脂粉体、分散
剤としてフッ素系アクリルオリゴマーを用意した。
Example 22 In addition to the charge transport substance, additives, and polycarbonate resin used in Example 1, polytetrafluoroethylene resin powder and a fluorine-based acrylic oligomer were prepared as a dispersant.

先ず、ポリカーボネート樹脂20部、ヒドラゾン化合物
20部及びフッ素系アクリルオリゴマー0.6部をモノ
クロルベンゼン100部に溶解する。ついでこの中に4
フツ化エチレン樹脂粉体6部を加え、ステンレス製ボー
ルミルで40時間分散し、更に添加剤T)(PM−1,
BZT−1各々1部をとかしたジクロルメタン溶液20
部を加えて電荷輸送層塗布液を調製した。この液を前記
電荷発生層上に塗布し、100℃、90分間熱風乾燥し
て20μm厚の電荷輸送層を形成した。
First, 20 parts of polycarbonate resin, 20 parts of hydrazone compound, and 0.6 part of fluorine-based acrylic oligomer are dissolved in 100 parts of monochlorobenzene. Then in this 4
Add 6 parts of fluorinated ethylene resin powder, disperse in a stainless steel ball mill for 40 hours, and add Additive T) (PM-1,
Dichloromethane solution containing 1 part of each of BZT-1 20
A charge transport layer coating solution was prepared. This liquid was applied onto the charge generation layer and dried with hot air at 100° C. for 90 minutes to form a charge transport layer with a thickness of 20 μm.

この感光体を実施例1で使用した複写機に搭載し、10
万枚の画出し耐久を行い、コピー画像を目視により観察
したが、画像ボケは発生しておらず高品位の画像を得る
ことができた。この時の表面層の膜厚削れ量は1.5μ
mであった。
This photoreceptor was installed in the copying machine used in Example 1, and 10
The copy image was visually observed after 10,000 sheets of image reproduction, and no image blurring occurred and a high-quality image could be obtained. At this time, the thickness of the surface layer was removed by 1.5μ.
It was m.

さらに、この感光体をそのまま複写機内に3日間放置し
た後コピーを行ったが、コピー画像上白ヌケは認められ
ず、高品位であった。
Further, this photoreceptor was left in a copying machine for 3 days and then copies were made, but no white spots were observed on the copied images and the quality was high.

実施例23〜29 滑材粉体としてポリ4フツ化エチレン樹脂粉体、ポリフ
ッ化ビニリデン樹脂粉体、ボリニフッ化二塩化エチレン
樹脂粉体、ポリエチレン粉体、ポリプロピレン粉体、フ
ッ化カーボンを電荷輸送物質として前記CT−1〜3を
、添加剤として第5表の化合物を用い、実施例22と同
様にして感光体を作成し評価を行った。結果を第5表に
示す。
Examples 23 to 29 As a lubricant powder, polytetrafluoroethylene resin powder, polyvinylidene fluoride resin powder, borinifluorodichloride ethylene resin powder, polyethylene powder, polypropylene powder, and carbon fluoride were used as a charge transport material Photoreceptors were prepared and evaluated in the same manner as in Example 22 using CT-1 to CT-3 as additives and the compounds shown in Table 5 as additives. The results are shown in Table 5.

以上の様に、酸化電位0.6v未満の電荷輸送物質に対
して特定の構造を有する2種以上の添加剤を添加して作
成した電子写真感光体は電荷輸送物質の劣化がないため
画像ボケが発生せず常に高品位の画像が得られるための
ものである。又、複写機内に長時間放置しても帯電器に
近接した部分に対応した白ヌケは発生せず常に高品位の
画像が得られるものである。
As described above, an electrophotographic photoreceptor made by adding two or more types of additives having a specific structure to a charge transport material with an oxidation potential of less than 0.6 V has no deterioration of the charge transport material, and therefore has no image blurring. This is to ensure that high-quality images can always be obtained without the occurrence of problems. Further, even if the copying machine is left in a copying machine for a long time, white spots corresponding to the portions close to the charger do not occur, and high-quality images are always obtained.

更に各種の滑材粉体を添加したものは10万枚耐久後も
常に高品位の画像を得ることができ、高耐久性感光体を
実現したものである。
Further, when various types of lubricant powders are added, high-quality images can always be obtained even after 100,000 sheets of printing, and a highly durable photoreceptor has been realized.

〔発明の効果〕〔Effect of the invention〕

以上の様に本発明の酸化電位が0.6v未満の電荷輸送
物質及び特定の構造を有する2種以上の添加剤を含有す
る電子写真感光体はコロナ放電環境下における耐久性が
極めて高く、常に安定した高品位の画像を得ることがで
きる。更に各種滑材粉体との組み合せは機械的耐久性も
向上され、高耐久な電子写真感光体を得ることができる
ものである。
As described above, the electrophotographic photoreceptor of the present invention containing a charge transport substance with an oxidation potential of less than 0.6 V and two or more types of additives having a specific structure has extremely high durability in a corona discharge environment, and is constantly Stable, high-quality images can be obtained. Furthermore, the combination with various lubricant powders improves mechanical durability, making it possible to obtain a highly durable electrophotographic photoreceptor.

Claims (2)

【特許請求の範囲】[Claims] (1)導電性基体上に感光層を有する電子写真感光体に
おいて、表面層が酸化電位0.6V未満の電荷輸送物質
と、下記一般式(1)および(2)で表わさるれる化合
物とを含有する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▼(1) (式中、 X_1は▲数式、化学式、表等があります▼または▲数
式、化学式、表等があります▼を表わし X_2はH、2〜10個の炭素を有するアルケニル基1
〜10個の炭素を有するアルキル基 を表わす。) ▲数式、化学式、表等があります▼(2) (式中、Rは、ハロゲン原子またはHを表わし、X_1
およびX_2は、炭素数1〜10個のアルキル基または
炭素数2〜10個のアルケニル基 を表わす。)
(1) In an electrophotographic photoreceptor having a photosensitive layer on a conductive substrate, the surface layer contains a charge transport material with an oxidation potential of less than 0.6 V and a compound represented by the following general formulas (1) and (2). An electrophotographic photoreceptor comprising: ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (1) (In the formula, X_1 represents ▲There are mathematical formulas, chemical formulas, tables, etc.▼ or ▲There are mathematical formulas, chemical formulas, tables, etc.▼, and X_2 is H, 2 to 10. Alkenyl group having carbon 1
represents an alkyl group having ~10 carbons. ) ▲There are mathematical formulas, chemical formulas, tables, etc.▼(2) (In the formula, R represents a halogen atom or H, and X_1
and X_2 represents an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms. )
(2)前記表面層がフッ素系樹脂粉体、ポリオレフィン
系粉体、およびフッ化カーボン粉体からなる群より選ば
れた滑材粉体を含有する特許請求の範囲第1項記載の電
子写真感光体。
(2) The electrophotographic photosensitive material according to claim 1, wherein the surface layer contains a lubricant powder selected from the group consisting of fluororesin powder, polyolefin powder, and fluorocarbon powder. body.
JP63216911A 1988-08-31 1988-08-31 Electrophotographic photoreceptor Expired - Fee Related JP2683054B2 (en)

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JP63216911A JP2683054B2 (en) 1988-08-31 1988-08-31 Electrophotographic photoreceptor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63216911A JP2683054B2 (en) 1988-08-31 1988-08-31 Electrophotographic photoreceptor

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Publication Number Publication Date
JPH0264550A true JPH0264550A (en) 1990-03-05
JP2683054B2 JP2683054B2 (en) 1997-11-26

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Country Status (1)

Country Link
JP (1) JP2683054B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7544451B2 (en) * 2005-07-28 2009-06-09 Xerox Corporation Photoreceptor layer having antioxidant lubricant additives

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JPS6356658A (en) * 1986-08-28 1988-03-11 Canon Inc Electrophotographic sensitive body
JPS63155049A (en) * 1986-12-18 1988-06-28 Konica Corp Electrophotographic positive charge sensitive body and image forming process thereof
JPS63168654A (en) * 1986-12-30 1988-07-12 Konica Corp Photosensitive body

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JPS62192754A (en) * 1986-02-20 1987-08-24 Canon Inc Electrophotographic sensitive body
JPS62272282A (en) * 1986-05-21 1987-11-26 Canon Inc Electrophotographic sensitive body
JPS6344662A (en) * 1986-08-11 1988-02-25 Konica Corp Positively electrifiable electrophotographic sensitive body
JPS6356658A (en) * 1986-08-28 1988-03-11 Canon Inc Electrophotographic sensitive body
JPS63155049A (en) * 1986-12-18 1988-06-28 Konica Corp Electrophotographic positive charge sensitive body and image forming process thereof
JPS63168654A (en) * 1986-12-30 1988-07-12 Konica Corp Photosensitive body

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