JPH07175231A - Single-layer electrophotographic photoreceptor - Google Patents

Single-layer electrophotographic photoreceptor

Info

Publication number
JPH07175231A
JPH07175231A JP34485593A JP34485593A JPH07175231A JP H07175231 A JPH07175231 A JP H07175231A JP 34485593 A JP34485593 A JP 34485593A JP 34485593 A JP34485593 A JP 34485593A JP H07175231 A JPH07175231 A JP H07175231A
Authority
JP
Japan
Prior art keywords
compound
layer
photosensitive layer
organic
substituted
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
JP34485593A
Other languages
Japanese (ja)
Inventor
Masayuki Shiyoji
正幸 所司
Yumi Ichikawa
由美 市川
Akio Kojima
明夫 小島
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.)
Ricoh Co Ltd
Original Assignee
Ricoh 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 Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP34485593A priority Critical patent/JPH07175231A/en
Publication of JPH07175231A publication Critical patent/JPH07175231A/en
Pending legal-status Critical Current

Links

Landscapes

  • Photoreceptors In Electrophotography (AREA)

Abstract

PURPOSE:To provide a single-layer electrophotographic photoreceptor excellent in electrostatic chargeability and sensitivity and excellent in the stability of the static charge characteristic even at the time of repeating copy process. CONSTITUTION:The single-layer electrophotographic photoreceptor has a photosensitive layer 2 obtained by dispersing at least a charge generating material 21, an organic positive hole moving material and an organic acceptor type compound into a binder and using a phthalimide compound as the organic acceptor type compound.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は電子写真用感光体に関
し、詳しくは、電子写真プロセスを用いた複写機、プリ
ンター等に用いられる単層型電子写真用感光体に関する
ものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrophotographic photoconductor, and more particularly to a single-layer type electrophotographic photoconductor used in a copying machine, a printer or the like using an electrophotographic process.

【0002】[0002]

【従来の技術】電子写真プロセスは静電力による潜像の
可視化を原理として用いたものであるため、そのプロセ
スの実施に用いられる電子写真用感光体には、暗所での
良好な帯電性と光照射による迅速な表面電位の減衰とが
要求される。かかるプロセス上で電子写真用感光体に必
要な特性は、固体物性値である暗抵抗の高さと良好な量
子効率、高い電荷移動度等に依存している。
2. Description of the Related Art Since an electrophotographic process is based on the principle of visualizing a latent image by electrostatic force, an electrophotographic photosensitive member used for carrying out the process has a good charging property in a dark place. Rapid surface potential decay due to light irradiation is required. The characteristics required for the electrophotographic photoreceptor in such a process depend on the height of dark resistance, which is a physical property value, good quantum efficiency, high charge mobility, and the like.

【0003】これらの物性値を満足するものとして、従
来より、セレン、セレン−テルル合金、砒化セレン等の
無機化合物から構成された感光体が採用され多くの複写
機で用いられてきた。しかしながら、これらの材料は毒
性が強い、アモルファス状態で用いられるため取扱いが
厄介である、数十μmの厚さに真空蒸着する必要からコ
スト高である等の欠点があり、感光体として未解決の問
題を有しているものであった。
As a material satisfying these physical property values, a photoconductor composed of an inorganic compound such as selenium, selenium-tellurium alloy, or selenium arsenide has been conventionally adopted and used in many copying machines. However, these materials have drawbacks that they are highly toxic, are difficult to handle because they are used in an amorphous state, and are high in cost because they need to be vacuum-deposited to a thickness of several tens of μm, and are unsolved as a photoreceptor. It had a problem.

【0004】これらの欠点を改良乃至解消するため、有
機材料を用いた電子写真感光体(OPC)の開発が積極
的になされ実用に供されるようになってきた。実用化さ
れたOPCのほとんどは、その感光層が電荷発生機能を
有する層(CGL)と電荷輸送機能を有する層(CT
L)とからなる積層型の構成であり、もっぱら負帯電プ
ロセスに用いられている。その理由は、使用される材料
を混合し、単に単層として形成した感光体では、帯電
性、感度、静電的特性の疲労現象が実用の程度以下まで
低下する欠点が露呈してしまう場合が多いのに対し、積
層型ではこれらの欠点が極力抑えられ、且つ、機械的強
度に富み、膜厚の設計が可能なCTLを表面に配置する
ことで、プロセスに供された状態で十分な機械的耐久性
を感光体に保持させることが可能となるからである。ま
た高速電子写真プロセスにおいても支障のない程度の高
い電荷移動度を示す有機材料は現在のところほとんど正
孔移動の性質のみを有するドナー化合物に限られ、ま
た、静電的性質の疲労現象を極力抑え且つプロセスに供
された状態で感光体の機械的な耐久性を充分保持させる
には、電荷発生と電荷移動との機能を層ごとに分離した
機能分離構造とし、正孔移動性のCTLを表面に配置し
た積層型の感光体が静電特性面では最も合理的なものと
されたからである。しかしながら、このような機能分離
構造の電子写真用感光体は新たな問題を生じさせている
のが実情である。
In order to improve or eliminate these drawbacks, electrophotographic photoreceptors (OPC) using organic materials have been actively developed and put into practical use. In most of the practically used OPCs, the photosensitive layer has a layer having a charge generation function (CGL) and a layer having a charge transport function (CT).
L) and a laminated structure, which is used exclusively in the negative charging process. The reason is that the photoconductor formed by mixing the materials to be used and simply forming it as a single layer may expose the drawback that the fatigue phenomenon of charging property, sensitivity, and electrostatic properties is reduced to a level below the level of practical use. On the other hand, in the laminated type, these drawbacks are suppressed as much as possible, and the CTLs, which are rich in mechanical strength and capable of designing the film thickness, are arranged on the surface, so that the machine can be sufficiently machined in the state of being used in the process. This is because it becomes possible to maintain the photoconductor with the desired durability. In addition, organic materials exhibiting high charge mobility that does not hinder high-speed electrophotographic processes are currently limited to donor compounds having only hole-transporting properties, and the fatigue phenomenon of electrostatic properties is minimized. In order to suppress the mechanical durability of the photoconductor sufficiently while keeping it in the process, a function separation structure in which the functions of charge generation and charge transfer are separated for each layer is used, and This is because the laminated-type photoconductor disposed on the surface is the most rational in terms of electrostatic characteristics. However, the electrophotographic photoconductor having such a function-separated structure actually causes a new problem.

【0005】その1つ目は感光体の負帯電に由来するも
のである。電子写真プロセスにおける信頼性の高い帯電
方式はコロナ放電によるものであり、ほとんどの複写
機、プリンタにはこの方式が採用されている。だが周知
のごとく、正極性と較べ負極性のコロナ放電は不安定で
あり、このためスコロトロンによる帯電方式が採用され
コストアップの一要因となっている。また、負極性のコ
ロナ放電はオゾンの発生をより多く伴うため、その外部
排出を防ぐべく負帯電方式の複写機、プリンタにはオゾ
ンフィルタが用いられている。正帯電方式であればオゾ
ン発生量は非常に少なく抑えられる。また、現状では環
境変動が少なく安定な画像が得られる二成分系現像剤の
トナーは正帯電用であり、この面からも正帯電用の感光
体が望ましい。
The first is derived from the negative charging of the photoconductor. A highly reliable charging method in the electrophotographic process is based on corona discharge, and this method is used in most copying machines and printers. However, as is well known, the negative polarity corona discharge is unstable as compared with the positive polarity, so that the charging method by the scorotron is adopted, which is one of the factors for the cost increase. Further, since negative corona discharge is accompanied by more generation of ozone, an ozone filter is used in a negative charging type copying machine or printer in order to prevent external discharge thereof. With the positive charging method, the ozone generation amount can be suppressed to a very small amount. Further, at present, the toner of the two-component type developer, which is capable of obtaining a stable image with little environmental change, is for positive charging, and from this aspect, a positive charging photoreceptor is desirable.

【0006】その2つ目は感光体の積層構造に由来する
ものである。感光体の製造では、真空蒸着法と較べ安価
な溶液塗布法を用いることが可能であるが、この様な積
層タイプの感光体を製造するためには少なくとも2回の
塗布操作、通常は感光体の帯電性確保のため基板のすぐ
上(基板と感光層との間)に下引き層を設けてあるため
3回の塗布操作が必要であり、これら複数回の塗布操作
は感光体のコストアップにつながる。さらに、感度及び
耐久性のバランスを保ちまた良好な画像を得るため、C
GLの厚さをサブミクロンの範囲で管理することも製造
コストを一層引き上げる要因となっている。
The second is derived from the laminated structure of the photoconductor. In the production of the photoconductor, it is possible to use a solution coating method which is less expensive than the vacuum vapor deposition method, but in order to produce such a laminated type photoconductor, at least two coating operations are usually performed. Since an undercoat layer is provided immediately above the substrate (between the substrate and the photosensitive layer) in order to ensure the charging property of 3 times, it is necessary to perform the coating operation three times, and the coating operation for plural times increases the cost of the photoconductor. Leads to. Furthermore, in order to maintain a good balance between sensitivity and durability and to obtain a good image, C
Controlling the thickness of the GL in the submicron range is another factor that further raises the manufacturing cost.

【0007】こうした問題を考慮すると、有機材料を用
いた電子写真感光体としては、正帯電プロセス用の単層
型(感光層が一層からなるタイプのもの)構成が望まし
いことが理解される。さらに、該感光体がそのまま、あ
るいは若干の変更で負帯電プロセスに用いることが可能
であれば、安価で使用環境の自由度が高い利点を有する
感光体を創製することが出来ることも理解される。しか
しながら、この条件を満足する感光体の例は非常に少な
い。単層型の有機感光体として市販されたものとして
は、ポリビニルカルバゾールとトリニトロフルオレノ
ンとからなる電荷移動錯体感光体、チアピリリウム染
料とポリカーボネートとからなる共晶錯体感光体、ペ
リレン系顔料及びヒドラゾンドナーが樹脂中に分散され
た感光体、等を数えるのみである。このうち、は負
帯電プロセスに用いられていたためオゾン発生の欠点を
伴っており、また、は感光体の感度が低いため、高速
の複写プロセスには不適な欠点を伴っていた。さらに、
実用化されている積層型感光体の成分を単に分散した場
合には、帯電電位と感度が低く、特に繰返し使用でそれ
らが大きく変動する欠点も克服出来ていない。
In view of these problems, it is understood that the electrophotographic photosensitive member using an organic material preferably has a single layer type (type having one photosensitive layer) structure for a positive charging process. Further, it is also understood that if the photoconductor can be used as it is or with a slight modification for the negative charging process, it is possible to create a photoconductor that is inexpensive and has a high degree of freedom in the usage environment. . However, there are very few examples of photoreceptors that satisfy this condition. Commercially available single-layer type organic photoconductors include charge transfer complex photoconductors composed of polyvinylcarbazole and trinitrofluorenone, eutectic complex photoconductors composed of thiapyrylium dye and polycarbonate, perylene pigments and hydrazone donors. It only counts the photoconductors, etc. dispersed in the resin. Of these, one was associated with the drawback of ozone generation because it was used in a negative charging process, and one was unsuitable for a high-speed copying process because of the low sensitivity of the photoconductor. further,
In the case where the components of the laminated-type photoconductor that have been put into practical use are simply dispersed, the charging potential and the sensitivity are low, and in particular, the drawback that they greatly fluctuate with repeated use cannot be overcome.

【0008】[0008]

【発明が解決しようとする課題】本発明の目的は、帯電
性、感度に優れ、また複写プロセスを繰返しても静電特
性の安定性に富んだ単層型電子写真用感光体を提供する
ことにある。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a single-layer type electrophotographic photosensitive member which is excellent in charging property and sensitivity, and which is stable in electrostatic characteristics even when a copying process is repeated. It is in.

【0009】[0009]

【課題を解決するための手段】本発明者らは、上記課題
を解決すべく鋭意検討した結果、少なくとも電荷発生物
質、有機正孔移動物質、有機アクセプター性化合物が結
着剤中に分散され、かつ有機アクセプター性化合物とし
て、フタルイミド化合物を用いた感光層を有する感光体
が上記目的に対して有効であることを見出し、本発明に
至った。すなわち、本発明によれば、導電性基体上に直
接又は下引き層を介して単層の感光層を設けてなり、そ
の感光層は少なくとも電荷発生物質、有機正孔移動物質
及び有機アクセプター性化合物が結着剤中に分散され、
かつ、該有機アクセプター性化合物がフタルイミド化合
物であることを特徴とする単層型電子写真用感光体が提
供される。
Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that at least a charge generating substance, an organic hole transfer substance, and an organic acceptor compound are dispersed in a binder. In addition, they have found that a photoreceptor having a photosensitive layer using a phthalimide compound as an organic acceptor compound is effective for the above purpose, and completed the present invention. That is, according to the present invention, a single photosensitive layer is provided on a conductive substrate directly or via an undercoat layer, and the photosensitive layer is at least a charge generating substance, an organic hole transporting substance and an organic acceptor compound. Are dispersed in the binder,
Further, there is provided a single-layer type electrophotographic photoreceptor, wherein the organic acceptor compound is a phthalimide compound.

【0010】このような感光体は帯電性と感度に優れ、
低速から高速の複写プロセスまで好適であり、また、電
荷発生物質を変えることで分光感度域が制御でき、モノ
クロ又はフルカラー用のアナログ複写機から光書き込み
用にLD光を使用したページプリンタの感光体にまで適
用することが可能となる。本発明に係わる感光層で特に
重要なのは有機アクセプター性化合物としてフタルイミ
ド化合物を用いたことである。このことにより、感光体
の高感度化、帯電特性及び静電特性の向上が図られる。
従来の単層型電子写真用感光体のうち電荷発生物質を樹
脂に分散させた形態のものでは電荷発生物質が電荷移動
機能も兼ねており、且つ、正孔及び電子の両方の電荷と
も移動特性が良好な顔料が少ないため、感度が低い、少
数電荷が蓄積し、繰り返しにより帯電電位が低下する等
の欠点や、光照射後直ちに光減衰が開始しない誘導期間
が存在し(インダクション効果)、静電潜像電位のラチ
チュードが狭い等の欠点があった。またこのような感光
体の正孔移動度を向上させるため、単に正孔移動物質を
添加した感光体では帯電性が低い、繰り返し使用で帯電
電位が著しく低下する等の欠点が克服出来てはいなかっ
た。本発明は少なくとも電荷発生物質、有機正孔移動物
質、有機アクセプター性化合物を結着剤中に分散し、該
有機アクセプター性化合物としてフタルイミド化合物を
用いることにより、上記の欠点を解消したものである。
この改良機構は現時点では定かでないが次のように推定
される。電荷発生物質は感光層中で粒子形態で存在して
いる。従って、光照射下で発生した電子の感光層中にお
ける移動は電荷発生物質粒子中と比べ電荷発生物質粒子
間で極めて悪くなり、この過程が感光層中に電子移動、
寿命を決定していると考えられる。このため、電荷発生
物質を分散保持しているマトリックス中に電子移動に優
れたアクセプター性化合物が存在すると、電子は電荷発
生物質粒子からアクセプター性化合物へ注入され、マト
リックスを通るスムーズな移動が達成できるものと考え
られる。フタルイミド化合物は電子を引き付ける能力が
高く、光照射により電荷発生物質中で発生した大多数の
電子をアクセプター性化合物側に移動させることが出
来、感光体の実用に支障を来さない帯電性、感度、静電
特性の長寿命化が実現される。さらに、本発明では正孔
移動に優れた正孔移動物質も樹脂マトリックス中に存在
しているため、感光層中の正孔移動もそれがないときに
比べスムーズになされる。
Such a photoreceptor has excellent chargeability and sensitivity,
Suitable for low-speed to high-speed copying processes, the spectral sensitivity range can be controlled by changing the charge generation material, and a photoconductor for a page printer using an LD light for optical writing from a monochrome or full-color analog copying machine. It is possible to apply to. Particularly important in the photosensitive layer according to the present invention is the use of a phthalimide compound as the organic acceptor compound. This makes it possible to increase the sensitivity of the photoconductor and improve the charging property and the electrostatic property.
Among the conventional single-layer type electrophotographic photoconductors in which the charge-generating substance is dispersed in the resin, the charge-generating substance also has a charge transfer function, and the charge characteristics of both holes and electrons are high. However, there are some defects such as low sensitivity, small number of electric charge accumulation, and decrease in charging potential due to repetition, and an induction period in which light decay does not start immediately after light irradiation (induction effect). There were drawbacks such as the latitude of the latent image potential was narrow. Further, in order to improve the hole mobility of such a photosensitive member, it is not possible to overcome the drawbacks such as the low charging property in a photosensitive member to which a hole transfer substance is simply added, and the charging potential is remarkably lowered by repeated use. It was The present invention solves the above-mentioned drawbacks by dispersing at least a charge generating substance, an organic hole transfer substance, and an organic acceptor compound in a binder and using a phthalimide compound as the organic acceptor compound.
This improvement mechanism is not clear at present, but it is estimated as follows. The charge generating substance is present in the photosensitive layer in the form of particles. Therefore, the movement of the electrons generated under the light irradiation in the photosensitive layer becomes extremely worse between the charge generating substance particles than in the charge generating substance particles, and this process causes the electron movement in the photosensitive layer.
It is considered that the life is determined. Therefore, when an acceptor compound excellent in electron transfer exists in the matrix that holds the charge generating substance dispersedly, electrons are injected from the charge generating substance particles into the acceptor compound, and smooth transfer through the matrix can be achieved. It is considered to be a thing. The phthalimide compound has a high ability to attract electrons, and can transfer most of the electrons generated in the charge generating substance by light irradiation to the acceptor compound side, and the charging property and sensitivity do not hinder the practical use of the photoconductor. The longevity of electrostatic characteristics is realized. Further, in the present invention, since the hole transfer material excellent in hole transfer is also present in the resin matrix, the hole transfer in the photosensitive layer is smoother than that in the absence thereof.

【0011】以下に本発明を添付の図面に沿って、さら
に詳細に説明する。図1は本発明に係わる感光体の一例
を示しており、1は導電性基体、2は感光層、21は電
荷発生物質、22は結着剤中に有機正孔移動物質と有機
アクセプター性化合物(フタルイミド化合物)とが分子
状に分散されたマトリックスを表わしている。
Hereinafter, the present invention will be described in more detail with reference to the accompanying drawings. FIG. 1 shows an example of a photoconductor according to the present invention, in which 1 is a conductive substrate, 2 is a photosensitive layer, 21 is a charge generating substance, 22 is an organic hole transfer substance and an organic acceptor compound in a binder. (Phthalimide compound) represents a matrix in which (phthalimide compound) is molecularly dispersed.

【0012】本発明の感光層2においては、前記したよ
うに有機アクセプター性化合物としてフタルイミド化合
物が用いられるが、かかるフタルイミド化合物としては
好適には下記一般式(I)で示される化合物が用いられ
る。
In the photosensitive layer 2 of the present invention, a phthalimide compound is used as the organic acceptor compound as described above, and as the phthalimide compound, a compound represented by the following general formula (I) is preferably used.

【化1】 (式中、R1及びR2は置換または無置換のアルキル基、
置換または無置換のシクロアルキル基、置換または無置
換のフェニル基、Xは=O、=C(Y)(Z)、=N
(CN)であり、Y及びZは水素原子、置換または無置
換のフェニル基、シアノ基、置換または無置換のアルコ
キシカルボニル基を表す。)
[Chemical 1] (In the formula, R 1 and R 2 are substituted or unsubstituted alkyl groups,
A substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted phenyl group, X is ═O, ═C (Y) (Z), ═N
(CN), Y and Z each represent a hydrogen atom, a substituted or unsubstituted phenyl group, a cyano group, or a substituted or unsubstituted alkoxycarbonyl group. )

【0013】前記一般式(I)で表わされるフタルイミ
ド化合物の具体例を下記表1に示すが、これらに限定さ
れるものではない。
Specific examples of the phthalimide compound represented by the general formula (I) are shown in Table 1 below, but the invention is not limited thereto.

【0014】[0014]

【表1−(1)】 [Table 1- (1)]

【0015】[0015]

【表1−(2)】 [Table 1- (2)]

【0016】[0016]

【表1−(3)】 [Table 1- (3)]

【0017】[0017]

【表1−(4)】 [Table 1- (4)]

【0018】[0018]

【表1−(5)】 [Table 1- (5)]

【0019】[0019]

【表1−(6)】 [Table 1- (6)]

【0020】[0020]

【表1−(7)】 [Table 1- (7)]

【0021】[0021]

【表1−(8)】 [Table 1- (8)]

【0022】[0022]

【表1−(9)】 [Table 1- (9)]

【0023】[0023]

【表1−(10)】 [Table 1- (10)]

【0024】[0024]

【表1−(11)】 [Table 1- (11)]

【0025】[0025]

【表1−(12)】 [Table 1- (12)]

【0026】[0026]

【表1−(13)】 [Table 1- (13)]

【0027】[0027]

【表1−(14)】 [Table 1- (14)]

【0028】次に、本発明の前記一般式(I)で表わさ
れるフタルイミド化合物の製造方法について説明する。
一般式(I)で表わされるフタルイミド化合物を製造す
るための反応式を下記表2に示す。前記一般式(I)で
表されるフタイミド化合物において、Xが=Oの化合物
は、一般に、3,3,4,4−ベンゾフェノンテトラカ
ルボン酸無水物(II)と下記アミン化合物(III)を反
応させることにより得ることができる。反応において必
要に応じて、例えば硫酸、パラトルエンスルホン酸など
の酸触媒、例えばピリジン、キノリン等の塩基触媒を使
用することができる。反応は通常無溶媒か、トルエン、
キシレン等の芳香族系溶媒、テトラヒドロフラン、1,
4−ジオキサン或いはN,Nジメチルホルムアミド等の
極性溶媒が使用され、反応温度は室温〜200℃で行な
われる。
Next, a method for producing the phthalimide compound represented by the general formula (I) of the present invention will be described.
The reaction formulas for producing the phthalimide compound represented by the general formula (I) are shown in Table 2 below. In the phthalimide compound represented by the general formula (I), a compound in which X is ═O is generally obtained by reacting 3,3,4,4-benzophenonetetracarboxylic acid anhydride (II) with the following amine compound (III). Can be obtained. In the reaction, if necessary, an acid catalyst such as sulfuric acid or p-toluenesulfonic acid, or a base catalyst such as pyridine or quinoline can be used. The reaction is usually solvent-free, toluene,
Aromatic solvents such as xylene, tetrahydrofuran, 1,
A polar solvent such as 4-dioxane or N, N dimethylformamide is used, and the reaction temperature is room temperature to 200 ° C.

【0029】本発明で用いる有機アクセプター性化合物
であるフタルイミド化合物の感光層2全体に占める量は
1〜40重量%、好ましくは5〜40重量%である。
The amount of the phthalimide compound which is an organic acceptor compound used in the present invention in the entire photosensitive layer 2 is 1 to 40% by weight, preferably 5 to 40% by weight.

【0030】本発明の感光層においては、必須成分とし
て有機正孔移動物質が含まれている。感光層中での正孔
移動物質の役割は電荷発生物質で発生した正孔を感光層
中で移動させることである。この移動機能により電荷発
生物質中で正孔が蓄積されず、電荷発生物質の電荷発生
機能を十分に発揮させることが可能となる。
The photosensitive layer of the present invention contains an organic hole transfer substance as an essential component. The role of the hole transfer material in the photosensitive layer is to transfer holes generated by the charge generating material in the photosensitive layer. Due to this transfer function, holes are not accumulated in the charge generating substance, and the charge generating function of the charge generating substance can be sufficiently exerted.

【0031】本発明で用いられる有機正孔移動物質とし
ては、分子中にトリフェニルアミン部位を有する化合
物、ヒドラゾン化合物、トリフェニルメタン化合物、ピ
ラゾリン化合物、オキサジアゾール化合物、カルバゾー
ル基を含む化合物、スチリル系化合物、ブタジエン系化
合物、ポリシラン化合物、ポリビニルカルバゾール等の
ドナー性化合物が挙げられる。有機正孔移動物質の感光
層2全体に占める量は15重量%以上好ましくは20〜
40重量%である。
Examples of the organic hole transfer substance used in the present invention include compounds having a triphenylamine moiety in the molecule, hydrazone compounds, triphenylmethane compounds, pyrazoline compounds, oxadiazole compounds, compounds containing a carbazole group, and styryl. Examples thereof include donor compounds such as system compounds, butadiene compounds, polysilane compounds, and polyvinylcarbazole. The amount of the organic hole transfer material in the entire photosensitive layer 2 is 15% by weight or more, preferably 20 to
It is 40% by weight.

【0032】感光層2における結着剤の役割は電荷発生
物質21の良好な分散と、有機正孔移動物質の分子状の
分散ばかりでなく、複写プロセスで必要とされる感光層
の機械的強度も担っている。このため、結着剤の組成比
が低い場合には、これらの諸性質が損なわれることとな
る。従って、感光層に占める結着剤の量はむやみに低く
はできない。これら結着剤の感光層全体に占める割合は
30〜90重量%好ましくは40〜70重量%が適当で
ある。本発明で用いられる結着剤としては、ポリエチレ
ン、ポリプロピレン、アクリル樹脂、メタクリル樹脂、
塩化ビニル樹脂、酢酸ビニル樹脂、エポキシ樹脂、ポリ
ウレタン樹脂、フェノール樹脂、ポリエステル樹脂、ア
ルキッド樹脂、ポリカーボネート樹脂、シリコーン樹
脂、メラミン樹脂等の付加重合型樹脂、重付加型樹脂、
重縮合型樹脂、並びにこれらの繰り返し単位のうち2つ
以上を含む共重合体樹脂、例えば塩化ビニル−酢酸ビニ
ル共重合体樹脂、塩化ビニル−酢酸ビニル−無水マレイ
ン酸共重合体樹脂などを挙げることができる。
The role of the binder in the photosensitive layer 2 is not only good dispersion of the charge generating substance 21 and molecular dispersion of the organic hole transporting substance, but also mechanical strength of the photosensitive layer required in the copying process. I am also responsible. Therefore, when the composition ratio of the binder is low, these properties will be impaired. Therefore, the amount of the binder in the photosensitive layer cannot be unnecessarily low. The proportion of these binders in the entire photosensitive layer is 30 to 90% by weight, preferably 40 to 70% by weight. As the binder used in the present invention, polyethylene, polypropylene, acrylic resin, methacrylic resin,
Vinyl chloride resin, vinyl acetate resin, epoxy resin, polyurethane resin, phenol resin, polyester resin, alkyd resin, polycarbonate resin, silicone resin, addition polymerization type resin such as melamine resin, polyaddition type resin,
Polycondensation type resins and copolymer resins containing two or more of these repeating units, such as vinyl chloride-vinyl acetate copolymer resins, vinyl chloride-vinyl acetate-maleic anhydride copolymer resins, etc. You can

【0033】本発明の単層型電子写真用感光体では電荷
発生物質も必須成分である。本発明で用いることのでき
る電荷発生物質としては、ビスアゾ顔料、トリスアゾ顔
料、フタロシアニン顔料、ペリレン顔料、キナクリドン
顔料、インジゴ顔料、多環キノン顔料等が挙げられる。
これらのうち、アゾ顔料の中心骨格としてはカルバゾー
ル基やスチリル基、ジフェニルアミン基、トリフェニル
アミン基のような電子供与性が好ましい。これら電荷発
生物質(顔料)の感光層2に占める量は0.1〜40重
量%好ましくは0.3〜25重量%くらいが適当であ
る。
In the single-layer type electrophotographic photoreceptor of the present invention, the charge generating substance is also an essential component. Examples of the charge generating substance that can be used in the present invention include bisazo pigments, trisazo pigments, phthalocyanine pigments, perylene pigments, quinacridone pigments, indigo pigments, and polycyclic quinone pigments.
Among these, as the central skeleton of the azo pigment, an electron donating property such as a carbazole group, a styryl group, a diphenylamine group or a triphenylamine group is preferable. The amount of these charge generating substances (pigments) in the photosensitive layer 2 is 0.1 to 40% by weight, preferably 0.3 to 25% by weight.

【0034】本発明の感光層2の厚さは5〜100μm
好ましくは10〜40μmくらいが適当である。5μm
より薄いと帯電性が低下し、逆に、100μmより厚い
と感度の低下をもたらす。
The thickness of the photosensitive layer 2 of the present invention is 5 to 100 μm.
It is preferably about 10 to 40 μm. 5 μm
When the thickness is thinner, the charging property is lowered, and conversely, when it is thicker than 100 μm, the sensitivity is lowered.

【0035】本発明で用いることができる導電性基体1
としては、アルミニウム、ニッケル、銅、ステンレス等
の金属板、金属ドラムまたは金属箔、アルミニウム、酸
化錫、ヨウ化銅などの薄膜を蒸着あるいは塗布したプラ
スチックフィルムあるいはガラス等が挙げられる。
Conductive substrate 1 that can be used in the present invention
Examples thereof include a metal plate such as aluminum, nickel, copper and stainless steel, a metal drum or a metal foil, a plastic film or glass on which a thin film such as aluminum, tin oxide and copper iodide is vapor-deposited or applied.

【0036】また、本発明の感光体では帯電性を改良す
る目的で、感光層2と導電性基体1との間に下引き層を
設けることができる。下引き層の材料としては前記結着
剤材料の他に、ポリアミド樹脂、ポリビニルアルコー
ル、カゼイン、ポリビニルピロリドン等を用いることが
できる。下引き層の厚さは0.01〜10μm好ましく
は0.1〜5μmくらいが適当である。
In the photoreceptor of the present invention, an undercoat layer may be provided between the photosensitive layer 2 and the conductive substrate 1 for the purpose of improving the charging property. As the material for the undercoat layer, polyamide resin, polyvinyl alcohol, casein, polyvinylpyrrolidone, or the like can be used in addition to the binder material. The thickness of the undercoat layer is 0.01 to 10 μm, preferably 0.1 to 5 μm.

【0037】本発明の感光体をつくるには、前記の材料
を有機溶媒中に溶解またはボールミル、超音波等で分散
して感光層形成液を調製し、これを浸漬法やブレード塗
布法、スプレー塗布法等で導電性基体1上に塗布し乾燥
して感光層2を形成すればよい。
To prepare the photoreceptor of the present invention, the above materials are dissolved in an organic solvent or dispersed by a ball mill, ultrasonic waves or the like to prepare a photosensitive layer forming liquid, which is then immersed, blade coated or sprayed. The photosensitive layer 2 may be formed by coating the conductive substrate 1 by a coating method or the like and drying it.

【0038】[0038]

【実施例】本発明を実施例により具体的に説明するが、
これにより本発明が限定されるものではない。
EXAMPLES The present invention will be specifically described with reference to Examples.
This does not limit the present invention.

【0039】実施例1 X型無金属フタロシアニン0.5gをポリカーボネート
Z(PC−Z、帝人化成社製)溶液10g(テトラヒド
ロフラン中に10重量%の濃度になるように溶解したも
の)、テトラヒドロフラン9gとともにボールミリング
した後、顔料組成2重量%、PC−Z組成が50重量
%、フタルイミド化合物(具体例NO.3)が20重量
%、下記化2で示される有機正孔移動物質が28%とな
るように10重量%のポリカーボネートZ溶液、フタル
イミド化合物、有機正孔移動物質を加え、十分に撹拌
し、感光層形成液を調整した。このようにして調製した
塗布液をアルミニウムを1000Åの厚さに蒸着した7
5μm厚のポリエステルフィルム上にドクターブレード
にて塗布し、乾燥後の膜厚が15μmの感光層を有する
単層型電子写真用感光体を作製した。
Example 1 0.5 g of X-type metal-free phthalocyanine was added together with 10 g of polycarbonate Z (PC-Z, Teijin Chemicals Co., Ltd.) solution (dissolved in tetrahydrofuran to a concentration of 10% by weight) and 9 g of tetrahydrofuran. After ball milling, the pigment composition is 2% by weight, the PC-Z composition is 50% by weight, the phthalimide compound (Specific Example No. 3) is 20% by weight, and the organic hole transfer substance represented by the following chemical formula 2 is 28%. Thus, a 10 wt% polycarbonate Z solution, a phthalimide compound, and an organic hole-transporting substance were added and sufficiently stirred to prepare a photosensitive layer forming liquid. The coating solution thus prepared was vapor-deposited with aluminum to a thickness of 1000Å.
A 5 μm thick polyester film was coated with a doctor blade, and a single-layer type electrophotographic photoreceptor having a photosensitive layer with a film thickness after drying of 15 μm was produced.

【化2】 [Chemical 2]

【0040】比較例1 実施例1において、フタルイミド化合物を除いた以外は
実施例1と同様の条件で感光体を作製した。
Comparative Example 1 A photoconductor was prepared under the same conditions as in Example 1 except that the phthalimide compound was omitted.

【0041】実施例2 実施例1において、フタルイミド化合物を具体例No.
6の化合物に代えた以外は実施例1と同様の条件で感光
体を作製した。
Example 2 In Example 1, the phthalimide compound was used as a specific example.
A photoconductor was prepared under the same conditions as in Example 1 except that the compound of 6 was used.

【0042】実施例3 実施例1において、フタルイミド化合物を具体例No.
36の化合物に代えた以外は実施例1と同様の条件で感
光体を作製した。以上のようにして作製した電子写真用
感光体を川口電機(株)製の静電複写紙試験装置(SP
−484)を用い、+6KVのコロナ放電を20秒間行
なって帯電せしめた後の表面電位Vs(V)、次いで2
0秒間暗減衰させ、その時の表面電位Vo(V)、及
び、その時点から感光体表面の照度が20ルックスにな
るようにしてタングステン光を照射し、Voが1/2に
なるのに要する露光量E1/2(ルックス・秒)、光照射
30秒後の表面電位V30(V)を測定した。測定結果を
表2に示す。
Example 3 In Example 1, the phthalimide compound was used as a specific example.
A photoconductor was prepared under the same conditions as in Example 1 except that the compound of 36 was used instead. The electrophotographic photosensitive member manufactured as described above was used as an electrostatic copying paper test device (SP) manufactured by Kawaguchi Electric Co., Ltd.
-484), the surface potential Vs (V) after the corona discharge of +6 KV was performed for 20 seconds to charge, and then 2
Dark decay for 0 seconds, and then the surface potential Vo (V) at that time and from that time, the tungsten light is irradiated so that the illuminance on the photoconductor surface becomes 20 lux, and the exposure required for Vo to become 1/2. The amount of E1 / 2 (lux · sec) and the surface potential V30 (V) after 30 seconds of light irradiation were measured. The measurement results are shown in Table 2.

【表2】 表2より、本発明の電子写真用感光体は感度、帯電性に
優れた特性を示すことがわかる。
[Table 2] From Table 2, it can be seen that the electrophotographic photosensitive member of the present invention exhibits excellent characteristics in sensitivity and chargeability.

【0043】[0043]

【発明の効果】本発明の単層型電子写真用感光体は帯電
性、感度に優れ、また複写プロセスを繰返しても静電特
性の安定性に富んだものである。
The single-layer type electrophotographic photoreceptor of the present invention is excellent in charging property and sensitivity, and is excellent in stability of electrostatic characteristics even when the copying process is repeated.

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

【図1】本発明に係わる単層型電子写真用感光体の一例
の概略図。
FIG. 1 is a schematic view of an example of a single-layer type electrophotographic photoconductor according to the present invention.

【符号の説明】[Explanation of symbols]

1 導電性基体 2 感光層 21 電荷発生顔料 22 結着剤マトリックス中に有機正孔移動物質と有機
アクセプター性化合物とが分子状に分散された層
DESCRIPTION OF SYMBOLS 1 Conductive substrate 2 Photosensitive layer 21 Charge generation pigment 22 Binder layer A layer in which an organic hole transfer substance and an organic acceptor compound are molecularly dispersed

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 導電性基体上に直接又は下引き層を介し
て単層の感光層を設けてなり、その感光層は少なくとも
電荷発生物質、有機正孔移動物質及び有機アクセプター
性化合物が結着剤中に分散され、かつ、該有機アクセプ
ター性化合物がフタルイミド化合物であることを特徴と
する単層型電子写真用感光体。
1. A single photosensitive layer is provided on a conductive substrate directly or via an undercoat layer, and the photosensitive layer is bound with at least a charge generating substance, an organic hole transfer substance and an organic acceptor compound. A single-layer type electrophotographic photoreceptor which is dispersed in an agent and in which the organic acceptor compound is a phthalimide compound.
【請求項2】 フタルイミド化合物が下記一般式1(化
1)で表わされる化合物であることを特徴とする請求項
1記載の単層型電子写真用感光体。 【化1】 (式中、R1及びR2は置換または無置換のアルキル基、
置換または無置換のシクロアルキル基、置換または無置
換のフェニル基、Xは=O、=C(Y)(Z)、=N
(CN)であり、Y及びZは水素原子、置換または無置
換のフェニル基、シアノ基、置換または無置換のアルコ
キシカルボニル基を表す。)
2. The single-layer type electrophotographic photoreceptor according to claim 1, wherein the phthalimide compound is a compound represented by the following general formula 1 (formula 1). [Chemical 1] (In the formula, R 1 and R 2 are substituted or unsubstituted alkyl groups,
A substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted phenyl group, X is ═O, ═C (Y) (Z), ═N
(CN), Y and Z each represent a hydrogen atom, a substituted or unsubstituted phenyl group, a cyano group, or a substituted or unsubstituted alkoxycarbonyl group. )
JP34485593A 1993-12-20 1993-12-20 Single-layer electrophotographic photoreceptor Pending JPH07175231A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34485593A JPH07175231A (en) 1993-12-20 1993-12-20 Single-layer electrophotographic photoreceptor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34485593A JPH07175231A (en) 1993-12-20 1993-12-20 Single-layer electrophotographic photoreceptor

Publications (1)

Publication Number Publication Date
JPH07175231A true JPH07175231A (en) 1995-07-14

Family

ID=18372512

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34485593A Pending JPH07175231A (en) 1993-12-20 1993-12-20 Single-layer electrophotographic photoreceptor

Country Status (1)

Country Link
JP (1) JPH07175231A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010254608A (en) * 2009-04-23 2010-11-11 Idemitsu Kosan Co Ltd Phthalimide compound, naphthalimide compound, naphthalic anhydride compound, electron transporting material including these compounds and organic thin film solar cell
WO2015046214A1 (en) * 2013-09-24 2015-04-02 保土谷化学工業株式会社 Charge control agent and toner using same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010254608A (en) * 2009-04-23 2010-11-11 Idemitsu Kosan Co Ltd Phthalimide compound, naphthalimide compound, naphthalic anhydride compound, electron transporting material including these compounds and organic thin film solar cell
WO2015046214A1 (en) * 2013-09-24 2015-04-02 保土谷化学工業株式会社 Charge control agent and toner using same
JPWO2015046214A1 (en) * 2013-09-24 2017-03-09 保土谷化学工業株式会社 Charge control agent and toner using the same
US9835965B2 (en) 2013-09-24 2017-12-05 Hodogaya Chemical Co., Ltd. Charge control agent and toner using same

Similar Documents

Publication Publication Date Title
JPH06123981A (en) Single layer type electrophotographic sensitive body
JPH06123986A (en) Single layer type electrophotographic sensitive body
JPH075709A (en) Monolayer electrophotographic sensitive body
JPH07175231A (en) Single-layer electrophotographic photoreceptor
JPH07175235A (en) Single layer electrophotographic photoreceptor
JPH06258852A (en) Single layer tape electrophotographic sensitive body
JPH07175232A (en) Single-layered electrophotographic photoreceptor
JPH06123983A (en) Single-layer type electrophotographic sensitive body
JPH06123985A (en) Signal layer type electrophotographic sensitive body
JPH06123984A (en) Signal layer type electrophotographic sensitive body
JPH07333871A (en) Monolayer electrophotographic photoreceptor
JPH0659467A (en) Single layer positively charged electrophotographic sensitive body
JPH07175234A (en) Single layer electrophotographic photoreceptor
JP3486697B2 (en) Single-layer electrophotographic photoreceptor
JPH075706A (en) Monolayer electrophotographic sensitive body
JPH06123979A (en) Single layer type electrophotographic sensitive body
JPH07325411A (en) Single layer type electrophotographic photoreceptor
JPH06123980A (en) Single layer type electrophotographc sensitive body
JPH06123982A (en) Signal-layer type electrophotographic sensitive body
JPH07325410A (en) Single layer type electrophotographic photoreceptor
JPH06266127A (en) Single layer type electrophotographic sensitive body
JPH07199491A (en) Single-layer electrophotographic photoreceptor
JPH06266130A (en) Single layer type electrophotographic sensitive body
JPH08123054A (en) Monolayer electrophotographic photoreceptor
JPH06186760A (en) Single layer type electrophotographic sensitive body