JPH02254464A - Electrophotographic sensitive body - Google Patents

Electrophotographic sensitive body

Info

Publication number
JPH02254464A
JPH02254464A JP7519489A JP7519489A JPH02254464A JP H02254464 A JPH02254464 A JP H02254464A JP 7519489 A JP7519489 A JP 7519489A JP 7519489 A JP7519489 A JP 7519489A JP H02254464 A JPH02254464 A JP H02254464A
Authority
JP
Japan
Prior art keywords
layer
photosensitive layer
binder resin
polycarbonate
group
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
JP7519489A
Other languages
Japanese (ja)
Inventor
Fumio Kojima
文夫 小島
Kazuyuki Nakamura
和行 中村
Koichi Yamamoto
孝一 山本
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 JP7519489A priority Critical patent/JPH02254464A/en
Publication of JPH02254464A publication Critical patent/JPH02254464A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To enhance the surface hardness of a photosensitive layer and durability of a photosensitive body by incorporating a specified polycarbonate as a binder resin in the photosensitive layer. CONSTITUTION:The photosensitive layer of this photosensitive body contains as the binder resin the polycarbonate comprising repeating units of formula I in which R1 is methyl, isopropyl, or the like and R2 is alkyl or halogen. The polycarbonate can be produced by allowing to react a compound corresponding to the unit of formula I embodies by the unit of formula II with phosgen, and the photosensitive layer may be of a single layer structure or a laminate structure of an electric charge generating layer and a charge transfer layer.

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、更に詳しくは、特定
のポリカーボネート樹脂を結着樹脂として用いた電子写
真感光体に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to an electrophotographic photoreceptor, and more particularly to an electrophotographic photoreceptor using a specific polycarbonate resin as a binder resin.

従来の技術 近年、電子写真技術は、高速、かつ高印字品質が得られ
ると言う利点を有するため、複写機及びレーザービーム
プリンター等の分野において、著しく応用されている。
BACKGROUND OF THE INVENTION In recent years, electrophotographic technology has been widely applied in the fields of copying machines, laser beam printers, etc. because it has the advantage of being able to achieve high speed and high print quality.

これ等電子写真技術において用いられる電子写真感光体
としては、従来からセレン、セレン−テルル合金、セレ
ン−ひ素合金、硫化カドミウム等の無機光導電材料を用
いたものが広く知られている。一方、これ等無機光導電
材料を用いた電子写真感光体に比べ、安価で製造性及び
廃棄性の点で優れた利点を有する有機光導電材料を用い
た電子写真感光体の研究も活発化してきている。中でも
、露光により電荷を発生する電荷発生層と電荷を輸送す
る電荷輸送層を積層する機能分離型の有機積層型感光体
は、感度、帯電性及びその繰り返し安定性等、電子写真
特性の点で優れており、種々の提案がなされ、実用化さ
れている。
As electrophotographic photoreceptors used in these electrophotographic techniques, those using inorganic photoconductive materials such as selenium, selenium-tellurium alloy, selenium-arsenic alloy, and cadmium sulfide are widely known. On the other hand, research on electrophotographic photoreceptors using organic photoconductive materials, which have advantages over electrophotographic photoreceptors using inorganic photoconductive materials in terms of cost and ease of manufacture and disposal, has become active. ing. Among these, functionally separated organic laminated photoreceptors, in which a charge generation layer that generates charges upon exposure and a charge transport layer that transports charges, are stacked are superior in terms of electrophotographic properties such as sensitivity, chargeability, and repeated stability. It is excellent, and various proposals have been made and put into practical use.

これら有機積層型感光体では、上記の電子写真特性に関
しては十分な性能を示すものが開発されてきているが、
機械的外力に対する耐久性、即ち、トナー、現像剤、用
紙、クリーニング部材等からの直接的負担による感光体
表面の摩耗や傷等の発生及びトナーフィルミング等の異
物付着などによって、画質欠陥が生じる問題があり、感
光体寿命を制限している。
Some of these organic layered photoreceptors have been developed that exhibit sufficient electrophotographic properties as described above.
Durability against external mechanical forces, that is, image quality defects may occur due to abrasion or scratches on the surface of the photoreceptor due to direct loads from toner, developer, paper, cleaning members, etc., and due to foreign matter adhesion such as toner filming. problems and limit photoreceptor life.

これらの問題点を解決するために揮々の対策が検討され
ており、例えが、感光体表面層の結着樹脂として、ポリ
メチルメタクリレート、ポリエステル、ポリカーボネー
ト樹脂等を用いるものが提案されている(特開昭57−
4051号及び特開昭60−172044号公報)。
Various countermeasures are being considered to solve these problems, and for example, methods using polymethyl methacrylate, polyester, polycarbonate resin, etc. as a binder resin for the surface layer of the photoreceptor have been proposed ( Japanese Unexamined Patent Publication No. 57-
No. 4051 and JP-A-60-172044).

発明が解決しようとする課題 ところで、従来提案された樹脂を結着樹脂として用いる
と、比較的良好な耐久性の電子写真感光体が得られるが
、未だ充分満足できるものではない。すなわち、それ等
の樹脂を用いて形成された塗膜は、その鉛筆硬度がHB
ないしHの範囲にとどまり、したがって、形成される電
子写真感光体の表面硬度は充分満足できるものではなく
、4万ないし5万枚程度のコピー操作によって、感光層
表面の摩耗及び傷による画質欠陥が発生すると言う問題
が残されていた。したがって、従来から、高い表面硬度
を有する感光層が形成されるような結着樹脂の開発が望
まれていた。
Problems to be Solved by the Invention By the way, when conventionally proposed resins are used as binder resins, electrophotographic photoreceptors with relatively good durability can be obtained, but they are still not fully satisfactory. In other words, the paint film formed using these resins has a pencil hardness of HB.
Therefore, the surface hardness of the electrophotographic photoreceptor formed is not fully satisfactory, and image quality defects due to abrasion and scratches on the surface of the photosensitive layer occur after copying operations of about 40,000 to 50,000 sheets. There were still problems that would arise. Therefore, it has been desired to develop a binder resin that allows formation of a photosensitive layer having high surface hardness.

本発明は、上記のような実状に鑑みてなされたものであ
って、従来の技術における上記の問題点を解消すること
を目的とするものである。
The present invention has been made in view of the above-mentioned circumstances, and aims to solve the above-mentioned problems in the conventional technology.

すなわち、本発明の目的は、高い表面硬度の感光層を有
する電子写真感光体を提供することにある。
That is, an object of the present invention is to provide an electrophotographic photoreceptor having a photosensitive layer with high surface hardness.

課題を解決するための手段 本発明者等は、感光層の結着樹脂について、種々検討し
た結果、下記構造式(I)で示される繰り返し単位より
なるポリカーボネート樹脂が、極めて優れた表面硬度を
有し、それを用いることによって、上記の問題点、すな
わち、感光層表面の摩耗及び傷による画質欠陥の発生を
解消し、電子写真感光体の寿命を飛躍的に向上させるこ
とができることを見い出し、本発明を完成するに至った
Means for Solving the Problems As a result of various studies on the binder resin of the photosensitive layer, the present inventors have found that a polycarbonate resin consisting of repeating units represented by the following structural formula (I) has extremely excellent surface hardness. We have discovered that by using this, the above-mentioned problems, namely the occurrence of image quality defects due to abrasion and scratches on the surface of the photosensitive layer, can be solved, and the lifespan of electrophotographic photoreceptors can be dramatically improved, and we have published this book. The invention was completed.

本発明は、導電性基体上に感光層を設けてなる電子写真
感光体において、感光層が、結着樹脂として、下記構造
式(I)で示される繰り返し単位よりなるポリカーボネ
ート樹脂を含有することを特徴とする。
The present invention provides an electrophotographic photoreceptor comprising a photosensitive layer provided on a conductive substrate, in which the photosensitive layer contains a polycarbonate resin consisting of a repeating unit represented by the following structural formula (I) as a binder resin. Features.

(式中、Riはメチル基、イソプロピル基、イソブチル
基、フェニル基又はフェネチル基を表わし、R2はアル
キル基又はハロゲン原子を表わす)以下、本発明につい
て、詳細に説明する。
(In the formula, Ri represents a methyl group, isopropyl group, isobutyl group, phenyl group, or phenethyl group, and R2 represents an alkyl group or a halogen atom) The present invention will be explained in detail below.

本発明の電子写真感光体における導電性基体としては、
アルミニウム、真ちゅう、銅、ニッケル、鋼等の金属板
又は金属シート、プラスチックシート上に、アルミニウ
ム、ニッケル、クロム、チタン、パラジウム、酸化イン
ジウム、酸化錫、グラファイト等の導電性物質を蒸着、
スパッタリング、塗布等によりコーティングして導電化
処理を施したもの、或いはガラス、プラスチック板、布
、紙等を導電化処理したもの等を用いることができる。
The conductive substrate in the electrophotographic photoreceptor of the present invention includes:
Vapor deposition of conductive substances such as aluminum, nickel, chromium, titanium, palladium, indium oxide, tin oxide, graphite, etc. on metal plates such as aluminum, brass, copper, nickel, and steel, metal sheets, and plastic sheets.
It is possible to use materials that have been subjected to conductive treatment by coating by sputtering, coating, etc., or materials that have been subjected to conductive treatment such as glass, plastic plates, cloth, and paper.

上記導電性基板上には、必要に応じて、バリアー機能或
いは接着機能を有する下引き層を設けてもよい。下引き
層を構成する材料としては、ポリビニルブチラール、ポ
リビニルアルコール、カゼイン、ポリアミド、セルロー
ス、ゼラチン、ポリウレタン、ポリエステル等の樹脂、
酸化アルミニウム等の金属酸化物が使用できる。
An undercoat layer having a barrier function or an adhesive function may be provided on the conductive substrate, if necessary. Materials constituting the undercoat layer include resins such as polyvinyl butyral, polyvinyl alcohol, casein, polyamide, cellulose, gelatin, polyurethane, and polyester;
Metal oxides such as aluminum oxide can be used.

導電性基板上に形成される感光層は、単層構造であって
も、また、電荷発生層と電荷輸送層とに機能分離された
積層構造であってもよい。積層構造の場合、電荷発生層
と電荷輸送層の積層順序は、いずれが上層であってもよ
い。
The photosensitive layer formed on the conductive substrate may have a single layer structure, or may have a laminated structure in which a charge generation layer and a charge transport layer are functionally separated. In the case of a laminated structure, the charge generation layer and the charge transport layer may be stacked in any order.

これ等感光層は、電荷発生物質、電荷輸送物質、又はそ
れ等両者が結着樹脂中に含有された塗膜より構成される
These photosensitive layers are composed of a coating film containing a charge generating substance, a charge transporting substance, or both in a binder resin.

電荷発生物質としては、非晶質セレン、結晶性セレン、
セレン−テルル合金、セレン−ひ素合金、その他のセレ
ン化合物及び合金、酸化亜鉛、酸化チタン等の無機系光
導電体、フタロシアニン系、スクェアリウム系、アント
アントロン系、ペリレン系、アゾ系、アントラキノン系
、ピレン系、ピリリウム塩、チアピリリウム塩等の有機
顔料及び染料が用いられる。
As charge generating substances, amorphous selenium, crystalline selenium,
Selenium-tellurium alloy, selenium-arsenic alloy, other selenium compounds and alloys, inorganic photoconductors such as zinc oxide and titanium oxide, phthalocyanine-based, squalium-based, anthrone-based, perylene-based, azo-based, anthraquinone-based, Organic pigments and dyes such as pyrene, pyrylium salts, and thiapyrylium salts are used.

電荷輸送物質としては、p−ベンゾキノン、クロラニル
、ブロモアニル、アントラキノン等のキノン系化合物、
テトラシアノキノジメタン系化合物、2.4.7〜トリ
ニトロフルオレノン、2,4,5.7−チトラニトロフ
ルオレノン等のフルオレノン化合物、キサントン系化合
物、ベンゾフェノン系化合物、シアノビニル系化合物、
エチレン系化合物等の電子吸引性物質、アリールアルカ
ン系化合物、トリフェニルアミン系化合物、アリール置
換エチレン系化合物、ベンジジン系化合物、スチルベン
系化合物、アントラセン系化合物、或いはこれ等の化合
物からなる基を主鎖又は側鎖に有する重合体等の電子供
与性物質が用いられる。
As the charge transport substance, quinone compounds such as p-benzoquinone, chloranil, bromoanil, anthraquinone,
Tetracyanoquinodimethane compounds, fluorenone compounds such as 2.4.7-trinitrofluorenone and 2,4,5.7-titranitrofluorenone, xanthone compounds, benzophenone compounds, cyanovinyl compounds,
An electron-withdrawing substance such as an ethylene compound, an arylalkane compound, a triphenylamine compound, an aryl-substituted ethylene compound, a benzidine compound, a stilbene compound, an anthracene compound, or a group consisting of such compounds as the main chain. Alternatively, an electron-donating substance such as a polymer having a side chain is used.

本発明において、結着樹脂としては、上記構造式(1)
で示される繰り返し単位よりなるポリカーボネート樹脂
が使用される。感光層が電荷発生層と電荷輸送層とに機
能分離された積層構造を有する場合においては、上記構
造式(I)で示されるポリカーボネート樹脂は、電荷発
生層及び電荷輸送層のいずれの結着樹脂としても用いる
ことができるが、少なくとも表面を形成する層において
用いる必要がある。そして、特に、表面が電荷輸送層よ
りなる場合における結着樹脂として使用するのが好まし
い。
In the present invention, as the binder resin, the above structural formula (1) is used.
A polycarbonate resin consisting of the repeating unit shown is used. When the photosensitive layer has a laminated structure in which a charge generation layer and a charge transport layer are functionally separated, the polycarbonate resin represented by the above structural formula (I) may be used as a binder resin for either the charge generation layer or the charge transport layer. However, it needs to be used at least in the layer forming the surface. In particular, it is preferably used as a binder resin when the surface is comprised of a charge transport layer.

本発明において使用される上記構造式(I)で示される
繰り返し単位よりなるポリカーボネート樹脂は、粘度平
均分子量は、1万〜20万、好ましくは2万〜10万の
ものが好ましい。
The polycarbonate resin composed of repeating units represented by the structural formula (I) used in the present invention preferably has a viscosity average molecular weight of 10,000 to 200,000, preferably 20,000 to 100,000.

また、本発明において好適に使用できるポリカーボネー
ト樹脂としては、例えば、次の繰り返し単位よりなるも
のが例示できる。
Furthermore, examples of polycarbonate resins that can be suitably used in the present invention include those consisting of the following repeating units.

上記ポリカーボネート樹脂は、構造式(I)の繰り返し
単位に対応するビスフェノール化合物をホスゲンと反応
させることによって製造することができる。次に、その
代表例を示す。
The above polycarbonate resin can be produced by reacting a bisphenol compound corresponding to the repeating unit of structural formula (I) with phosgene. Next, a typical example is shown.

合成例1 2gの反応器に、4.4’−(1−メチルエチリデン)
ビス(2−メチルフェノール)0.2モル、4.7%濃
度の水酸化ナトリウム水溶液400 ml、及び塩化メ
チレン350 mlを添加し、激しく撹拌しながら、ホ
スゲンを400m1/分の割合で15分間吹き込んだ。
Synthesis Example 1 4.4'-(1-methylethylidene) was added to a 2g reactor.
0.2 mol of bis(2-methylphenol), 400 ml of a 4.7% aqueous sodium hydroxide solution, and 350 ml of methylene chloride were added, and while stirring vigorously, phosgene was blown in at a rate of 400 ml/min for 15 minutes. is.

反応温度を15℃に保ち、更に13.7%濃度の水酸化
ナトリウム40m1.  F’リメチルベンジルアンモ
ニウムクロライド0.2 g、及びトリエチルアミン0
.3mlを加え、23℃で1時間撹拌を続けて、重縮合
反応を実施した。反応終了後、生成物を塩化メチレン4
00 mlで希釈し、水t glo、oi規定の塩酸0
.5g、及び水1gで順次洗浄した。得られた有機層を
、5gのメタノールに注入して、白色重合体を沈澱させ
、濾別後、100℃で12時間乾燥して上記例示線り返
し単位(1)よりなるポリカーボネート樹脂的55gを
得た。
The reaction temperature was kept at 15°C, and 40ml of 13.7% sodium hydroxide was added. F'limethylbenzylammonium chloride 0.2 g, and triethylamine 0
.. 3 ml was added and stirring was continued for 1 hour at 23°C to carry out a polycondensation reaction. After the reaction is complete, the product is diluted with methylene chloride 4
Dilute with 0 ml of water, add 0 ml of normal hydrochloric acid
.. 5 g and 1 g of water. The obtained organic layer was poured into 5 g of methanol to precipitate a white polymer, which was filtered and dried at 100° C. for 12 hours to obtain 55 g of polycarbonate resin consisting of the above-mentioned exemplary linear repeating unit (1). Obtained.

合成例2 合成例1における、4.4’−(1−メチルエチリデン
)ビス(2−メチルフェノール)の代わりに、4゜4’
−(1,3−ジメチルブチリデン)ビス(2−メチルフ
ェノール)0.2モルを用いた以外は、合成例1と同様
に重縮合させて、上記例示線り返し単位(2)よりなる
ポリカーボネート樹脂的55gを得た。
Synthesis Example 2 In place of 4.4'-(1-methylethylidene)bis(2-methylphenol) in Synthesis Example 1, 4°4'
-(1,3-dimethylbutylidene)bis(2-methylphenol) 0.2 mole was used, but the polycondensation was carried out in the same manner as in Synthesis Example 1 to obtain a polycarbonate consisting of the above-mentioned exemplary linear repeating unit (2). 55 g of resin was obtained.

合成例3 合成例1における、4.4’−(1−メチルエチリデン
)ビス(2−メチルフェノール)の代わりに、4゜4’
−(1−フェニルエチリデン)ビス(2−メチルフェノ
ール)0.2モルを用いた以外は、合成例1と同様に重
縮合させて、上記例示線り返し単位(3)よりなるポリ
カーボネート樹脂的55gを得た。
Synthesis Example 3 Instead of 4.4'-(1-methylethylidene)bis(2-methylphenol) in Synthesis Example 1, 4°4'
- Polycondensation was carried out in the same manner as in Synthesis Example 1 except that 0.2 mol of (1-phenylethylidene)bis(2-methylphenol) was used to obtain 55 g of polycarbonate resin consisting of the above-mentioned exemplary linear repeating unit (3). I got it.

合成例4 合成例1における、4.4’−(1−メチルエチリデン
)ビス(2−メチルフェノール)の代わりに、4゜4’
−(L−メチル−8−フェニルプロピリデン)ビス(2
−メチルフェノール)0.2モルを用いた以外は、合成
例1と同様に重縮合させて、上記例示線り返し単位(4
)よりなるポリカーボネート樹脂的55gを得た 本発明において、感光層が積層措造を有する場合、電荷
発生層は、上記電荷発生物質及び結着樹脂を適当な溶媒
に分散又は溶解させて得た塗布液を塗布し、乾燥するこ
とによって形成することができる。結着樹脂としては、
上記の構造式(1)で示されるポリカーボネート樹脂の
ほか、結着樹脂として公知のもの、例えば、ポリスチレ
ン、ポリ塩化ビニル、ポリ酢酸ビニル、塩化ビニル−酢
酸ビニル共重合体、ポリビニルアセタール、アルキッド
樹脂、アクリル樹脂、ポリアクリロニトリル、ポリカー
ボネート、ポリアミド、ポリケトン、ポリアクリルアミ
ド、ブチラール樹脂、ポリエステル等の熱可塑性樹脂、
ポルウレタン、エポキシ樹脂、フェノール樹脂等の熱硬
化性樹脂等、従来公知のものが使用できる。
Synthesis Example 4 Instead of 4.4'-(1-methylethylidene)bis(2-methylphenol) in Synthesis Example 1, 4°4'
-(L-methyl-8-phenylpropylidene)bis(2
Polycondensation was carried out in the same manner as in Synthesis Example 1, except that 0.2 mol of the above-mentioned exemplified linear repeating unit (4
) In the present invention, when the photosensitive layer has a laminated structure, the charge generation layer is a coating obtained by dispersing or dissolving the above charge generation substance and binder resin in a suitable solvent. It can be formed by applying a liquid and drying it. As a binder resin,
In addition to the polycarbonate resin represented by the above structural formula (1), known binder resins such as polystyrene, polyvinyl chloride, polyvinyl acetate, vinyl chloride-vinyl acetate copolymer, polyvinyl acetal, alkyd resin, Thermoplastic resins such as acrylic resin, polyacrylonitrile, polycarbonate, polyamide, polyketone, polyacrylamide, butyral resin, polyester,
Conventionally known thermosetting resins such as polyurethane, epoxy resin, and phenol resin can be used.

電荷発生層の膜厚は、通常0.05〜40加、好ましく
は0.05〜25如に設定される。
The thickness of the charge generation layer is usually set to 0.05 to 40 mm, preferably 0.05 to 25 mm.

また、電荷輸送層は、上記した電荷輸送物質及び構造式
(I)で示されるポリカーボネート樹脂とを、適当な溶
媒に溶解させた溶液を塗布し、乾燥させることによって
形成することができる。電荷輸送層の形成に使用される
溶媒としては、代表的なものとして、例えば、ベンゼン
、トルエン、キシレン、クロルベンゼン等の芳香族系炭
化水素類、塩化メチレン、クロロホルム、塩化エチレン
等のハロゲン化脂肪族系炭化水素類、テトラヒドロフラ
ン、ジオキサン等の環状或いは直鎖状エーテル等、或い
はこれ等の混合溶剤をあげることができる。
Further, the charge transport layer can be formed by applying a solution in which the above charge transport substance and the polycarbonate resin represented by structural formula (I) are dissolved in an appropriate solvent, and drying the solution. Typical solvents used to form the charge transport layer include aromatic hydrocarbons such as benzene, toluene, xylene, and chlorobenzene, and halogenated fats such as methylene chloride, chloroform, and ethylene chloride. Examples include group hydrocarbons, cyclic or linear ethers such as tetrahydrofuran and dioxane, and mixed solvents thereof.

なお、電荷輸送層が表面層でない場合には、結着樹脂と
して従来公知のものを使用することもできる。
In addition, when the charge transport layer is not a surface layer, a conventionally known binder resin can also be used.

電荷輸送層の膜厚は、2〜100m+、好ましくはlO
〜40ρに設定される。
The thickness of the charge transport layer is 2 to 100 m+, preferably lO
~40ρ.

実施例 以下、本発明を実施例によって具体的に説明するが、本
発明がこれ等実施例に限定されるものではない。
EXAMPLES Hereinafter, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to these Examples.

実施例1 導電性基体として、アルミニウムパイプを用い、これに
ポリアミド樹脂10重量部、メタノール150重量部、
及び水40重量部からなる塗布液を塗布し、乾燥して、
膜厚1加の下引き層を形成した。更に三方晶系セレン(
米国ゼロラフスフ社製)90重量部、ポリビニルブチラ
ール樹脂10重量部、n−ブタノール300重量部から
なる混合物を分散させ、得られた分散液1重量部に対し
n−ブタノール2重量部を加えて稀釈した液を、上記の
下引き層上に塗布し、乾燥して、膜厚0.3 /IIJ
11の電荷発生層を形成した。次にN、N’−ジフェニ
ル−N、N’−ビス(3−メチルフェニル) −[1,
1’−ビフェニル]−4,4’−ジアミン3重量部と前
記合成例1において得られたポリカーボネート樹脂10
重量部とを塩化メチレン40ffl量部に加えて溶解し
、得られた溶液を、上記の電荷発生層上に塗布し、乾燥
して、膜厚20加の電荷輸送層を形成させ、二層からな
る電子写真感光体を作製した。
Example 1 An aluminum pipe was used as a conductive substrate, and 10 parts by weight of polyamide resin, 150 parts by weight of methanol,
and 40 parts by weight of water, and dried.
A subbing layer having a thickness of 1 mm was formed. Furthermore, trigonal selenium (
A mixture consisting of 90 parts by weight (manufactured by Zero Rafusuf Co., Ltd., USA), 10 parts by weight of polyvinyl butyral resin, and 300 parts by weight of n-butanol was dispersed, and 2 parts by weight of n-butanol was added to 1 part by weight of the resulting dispersion to dilute it. The liquid is applied onto the undercoat layer and dried to a film thickness of 0.3/IIJ.
Eleven charge generation layers were formed. Next, N,N'-diphenyl-N,N'-bis(3-methylphenyl)-[1,
3 parts by weight of 1'-biphenyl]-4,4'-diamine and 10 parts of the polycarbonate resin obtained in Synthesis Example 1
parts by weight are added to 40ffl parts of methylene chloride and dissolved, the resulting solution is applied onto the above charge generation layer and dried to form a charge transport layer with a thickness of 20%, and the two layers are separated. An electrophotographic photoreceptor was fabricated.

上記の様にして作製された電子写真感光体をクリーニン
グ部材を有する複写機に装着して10万枚のコピー走行
を行った場合における、電子写真感光体表面の摩耗及び
傷による画像欠陥発生の有無、及び表面摩耗量を調査し
た。更にまた、表面鉛筆硬度を調べた。結果を第1表に
示す。
When the electrophotographic photoreceptor produced as described above is installed in a copying machine equipped with a cleaning member and copies are made for 100,000 copies, is there any occurrence of image defects due to abrasion and scratches on the surface of the electrophotographic photoreceptor? , and the amount of surface wear were investigated. Furthermore, the surface pencil hardness was examined. The results are shown in Table 1.

実施例2〜4 電荷輸送層の結着樹脂として、前記合成例2〜4で得ら
れたポリカーボネート樹脂を用いた以外は、すべて上記
実施例と同様に処理して電子写真感光体を作製し、同様
に評価を行なった。それ等の結果を第1表に示す。
Examples 2 to 4 Electrophotographic photoreceptors were prepared in the same manner as in the above Examples except that the polycarbonate resins obtained in Synthesis Examples 2 to 4 were used as the binder resin of the charge transport layer. Evaluation was conducted in the same manner. The results are shown in Table 1.

比較例1 電荷輸送層の結着樹脂として、下記構造式で示される繰
り返し単位からなるポリカーボネート樹脂を用いた以外
は、すべて上記実施例と同様に処理して電子写真感光体
を作製し、同様に評価を行なった。結果を第1表に示す
Comparative Example 1 An electrophotographic photoreceptor was prepared in the same manner as in the above Example except that a polycarbonate resin consisting of a repeating unit represented by the following structural formula was used as the binder resin of the charge transport layer. We conducted an evaluation. The results are shown in Table 1.

第1表 比較例2 電荷輸送層の結着樹脂として、下記構造式で示される繰
り返し単位からなるポリカーボネート樹脂を用いた以外
は、すべて上記実施例と同様に処理して電子写真感光体
を作製し、同様に評価を行なった。結果を第1表に示す
Table 1 Comparative Example 2 An electrophotographic photoreceptor was prepared in the same manner as in the above example except that a polycarbonate resin consisting of a repeating unit represented by the following structural formula was used as the binder resin of the charge transport layer. , similarly evaluated. The results are shown in Table 1.

発明の効果 本発明においては、感光層の結着樹脂として、上記構造
式(1)で示される繰り返し単位よりなるポリカーボネ
ート樹脂を用いたから、形成された塗膜は極めて優れた
表面硬度を有しており、したがって本発明の電子写真感
光体は、耐久性に優れ、感光層表面の摩耗及び傷による
画像欠陥の発生が抑制され、寿命が飛躍的に向上する。
Effects of the Invention In the present invention, since a polycarbonate resin consisting of repeating units represented by the above structural formula (1) is used as the binder resin of the photosensitive layer, the formed coating film has extremely excellent surface hardness. Therefore, the electrophotographic photoreceptor of the present invention has excellent durability, suppresses the occurrence of image defects due to abrasion and scratches on the surface of the photosensitive layer, and dramatically improves the service life.

特許出願人  富士ゼロックス株式会社代理人    
弁理士  製部 剛
Patent applicant Fuji Xerox Co., Ltd. Agent
Patent attorney Tsuyoshi Seibe

Claims (1)

【特許請求の範囲】[Claims] (1)導電性基体上に感光層を設けてなる電子写真感光
体において、該感光層が、結着樹脂として、下記構造式
( I )で示される繰り返し単位よりなるポリカーボネ
ート樹脂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▼( I ) (式中、R_1はメチル基、イソプロピル基、イソブチ
ル基、フェニル基又はフェネチル基を表わし、R_2は
アルキル基又はハロゲン原子を表わす)
(1) In an electrophotographic photoreceptor comprising a photosensitive layer provided on a conductive substrate, the photosensitive layer contains a polycarbonate resin consisting of a repeating unit represented by the following structural formula (I) as a binder resin. Characteristic electrophotographic photoreceptor. ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (I) (In the formula, R_1 represents a methyl group, isopropyl group, isobutyl group, phenyl group, or phenethyl group, and R_2 represents an alkyl group or a halogen atom)
JP7519489A 1989-03-29 1989-03-29 Electrophotographic sensitive body Pending JPH02254464A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7519489A JPH02254464A (en) 1989-03-29 1989-03-29 Electrophotographic sensitive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7519489A JPH02254464A (en) 1989-03-29 1989-03-29 Electrophotographic sensitive body

Publications (1)

Publication Number Publication Date
JPH02254464A true JPH02254464A (en) 1990-10-15

Family

ID=13569141

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7519489A Pending JPH02254464A (en) 1989-03-29 1989-03-29 Electrophotographic sensitive body

Country Status (1)

Country Link
JP (1) JPH02254464A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5382489A (en) * 1992-08-06 1995-01-17 Fuji Xerox Co., Ltd. Electrophotographic photoreceptor with polycarbonate resin mixture
US5763126A (en) * 1995-06-01 1998-06-09 Sharp Kabushiki Kaisha Electrophotographic photoreceptor and production process for same
JP2016164651A (en) * 2015-02-27 2016-09-08 キヤノン株式会社 Electrophotographic photoreceptor, manufacturing method for the same, process cartridge and electrophotographic device
JP2018036630A (en) * 2016-08-26 2018-03-08 キヤノン株式会社 Electrophotographic photoreceptor, process cartridge, and electrophotographic apparatus

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57144555A (en) * 1981-03-02 1982-09-07 Fuji Xerox Co Ltd Electrophotographic receptor
JPS62135840A (en) * 1985-12-10 1987-06-18 Fuji Xerox Co Ltd Electrophotographic sensitive body
JPS63148263A (en) * 1986-12-12 1988-06-21 Mitsubishi Kasei Corp Electrophotographic sensitive body
JPS63206760A (en) * 1987-02-23 1988-08-26 Ricoh Co Ltd Electrophotographic sensitive body
JPH01273046A (en) * 1988-04-26 1989-10-31 Mitsubishi Kasei Corp Electrophotographic sensitive body
JPH01319750A (en) * 1988-06-22 1989-12-26 Asahi Chem Ind Co Ltd Electrophotographic sensitive body
JPH02132452A (en) * 1988-11-14 1990-05-21 Konica Corp Electrophotographic sensitive body

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57144555A (en) * 1981-03-02 1982-09-07 Fuji Xerox Co Ltd Electrophotographic receptor
JPS62135840A (en) * 1985-12-10 1987-06-18 Fuji Xerox Co Ltd Electrophotographic sensitive body
JPS63148263A (en) * 1986-12-12 1988-06-21 Mitsubishi Kasei Corp Electrophotographic sensitive body
JPS63206760A (en) * 1987-02-23 1988-08-26 Ricoh Co Ltd Electrophotographic sensitive body
JPH01273046A (en) * 1988-04-26 1989-10-31 Mitsubishi Kasei Corp Electrophotographic sensitive body
JPH01319750A (en) * 1988-06-22 1989-12-26 Asahi Chem Ind Co Ltd Electrophotographic sensitive body
JPH02132452A (en) * 1988-11-14 1990-05-21 Konica Corp Electrophotographic sensitive body

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5382489A (en) * 1992-08-06 1995-01-17 Fuji Xerox Co., Ltd. Electrophotographic photoreceptor with polycarbonate resin mixture
US5763126A (en) * 1995-06-01 1998-06-09 Sharp Kabushiki Kaisha Electrophotographic photoreceptor and production process for same
JP2016164651A (en) * 2015-02-27 2016-09-08 キヤノン株式会社 Electrophotographic photoreceptor, manufacturing method for the same, process cartridge and electrophotographic device
JP2018036630A (en) * 2016-08-26 2018-03-08 キヤノン株式会社 Electrophotographic photoreceptor, process cartridge, and electrophotographic apparatus

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