JP2001142237A - Electrophotographic photoreceptor - Google Patents
Electrophotographic photoreceptorInfo
- Publication number
- JP2001142237A JP2001142237A JP32630299A JP32630299A JP2001142237A JP 2001142237 A JP2001142237 A JP 2001142237A JP 32630299 A JP32630299 A JP 32630299A JP 32630299 A JP32630299 A JP 32630299A JP 2001142237 A JP2001142237 A JP 2001142237A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- photoreceptor
- layer
- derivatives
- photosensitive layer
- 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
Links
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- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- 150000007978 oxazole derivatives Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 125000001791 phenazinyl group Chemical class C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 125000005506 phthalide group Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical class C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 229960005265 selenium sulfide Drugs 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000010301 surface-oxidation reaction Methods 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 150000007979 thiazole derivatives Chemical class 0.000 description 1
- 238000002366 time-of-flight method Methods 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Photoreceptors In Electrophotography (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、電子写真用に有機
感光体に関し、より詳しくは、単層型の正帯電用電子写
真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 organic photoreceptor for electrophotography, and more particularly to a single-layer type electrophotographic photoreceptor for positive charging.
【0002】[0002]
【従来の技術】従来、電子写真用感光体の感光層にはセ
レン、硫化カドミウム、酸化亜鉛等の無機系の光導電性
物質が広く用いられていた。しかしながら、セレン、硫
化カドミウムは毒物として回収が必要であり、セレンは
熱により結晶化するために耐熱性に劣り、硫化カドミウ
ム、酸化亜鉛は耐湿性に劣り、また酸化亜鉛は耐刷性が
ないなどの欠点を有している。近年では、有機系の光導
電性物質を電子写真用感光体の感光層に用いる研究が大
きく進展し、その特性も多くの点で無機感光体を凌ぐよ
うになり、複写機、プリンターに搭載される感光体の大
部分が有機系の感光体になるに至っている。有機系の光
導電性物質は無機系のものに比し、成膜が容易でかつ低
コストである、長波長光源に対する感度が得やすい、材
料の毒性が無い、感光層の組成選択の余地が大きい、種
類によっては透明な感光体を製造できる、可とう性を有
し、ベルト状に加工可能である、等の利点を有する。2. Description of the Related Art Conventionally, inorganic photoconductive substances such as selenium, cadmium sulfide, and zinc oxide have been widely used for a photosensitive layer of an electrophotographic photosensitive member. However, selenium and cadmium sulfide need to be recovered as poisons, selenium crystallizes by heat and therefore has poor heat resistance, cadmium sulfide and zinc oxide have poor moisture resistance, and zinc oxide has no printing durability. Has the disadvantage of In recent years, research on using an organic photoconductive substance for the photosensitive layer of an electrophotographic photoreceptor has made great progress, and its characteristics have surpassed inorganic photoreceptors in many respects. Most photoconductors have become organic photoconductors. Organic photoconductive materials are easier to deposit and are less costly than inorganic ones, are easily sensitive to long-wavelength light sources, have no toxicity of materials, and there is room for selection of photosensitive layer composition. It has the advantages that it can be large, can produce a transparent photoreceptor depending on the type, has flexibility, and can be processed into a belt shape.
【0003】有機系電子写真感光体においては、電荷キ
ャリアーの発生と移動の機能を別々の化合物に分担させ
る、いわゆる機能分離型の感光体が、材料選択の余地が
大きく、感光体の特性の制御がし易いことから、開発の
主流となっている。層構成の観点からは、電荷発生剤と
電荷輸送剤を同一の層中に有する単層型感光体と、別々
の層(電荷発生層と電荷輸送層)中に分離、積層する積
層型感光体が知られている。このうち積層型感光体は、
感光体設計上からは、 層ごとに機能の最適化が計りやす
く、特性の制御も容易なことから現行感光体の大部分は
このタイプになっている。このような積層型感光体のほ
とんどのものは、基体上に少なくとも電荷発生層、電荷
輸送層をこの順序で有している。該電荷輸送層において
は、好適な電子輸送材料がきわめて少ないのに対して、
正孔輸送材料は特性の良好な材料が数多く知られてい
る。そのため、このような正孔輸送材料を用いた積層型
感光体においては、帯電においては負帯電方式が採用さ
れる。このような負帯電方式において、負のコロナ放電
により感光体を帯電させる場合には発生するオゾンが環
境および感光体特性に悪影響を及ぼすことがある。[0003] In an organic electrophotographic photoreceptor, a so-called function-separated type photoreceptor in which the functions of generating and transferring charge carriers are shared by different compounds has much room for material selection and control of the characteristics of the photoreceptor. It is the mainstream of development because it is easy to do. From the viewpoint of the layer structure, a single-layer type photoreceptor having a charge generating agent and a charge transporting agent in the same layer, and a laminated type photoreceptor separated and laminated in separate layers (a charge generating layer and a charge transporting layer) It has been known. Of these, the stacked photoreceptor
Most of the current photoconductors are of this type from the viewpoint of photoconductor design because it is easy to optimize the function of each layer and control the characteristics. Most of such laminated photoconductors have at least a charge generation layer and a charge transport layer on a substrate in this order. In the charge transport layer, while there are very few suitable electron transport materials,
Many hole transporting materials having good properties are known. Therefore, in a stacked photoreceptor using such a hole transport material, a negative charging method is employed for charging. In such a negative charging system, when the photoconductor is charged by negative corona discharge, the generated ozone may adversely affect the environment and the characteristics of the photoconductor.
【0004】それに対し、特開昭61−77054、同
61−188543、特開平2−228670、特公平
7−97223、同7−97225号公報記載のような
単層型の正帯電感光体を使用する際には、そのようなオ
ゾン発生が低減されることが一つの利点と考えられてお
り、電気特性面では負帯電の積層型感光体より劣るもの
が多いものの、一部実用化されている。このようなオゾ
ン発生に対する効果の他にも、単層型感光体は、塗布工
程が少なくなる、半導体レーザー光に対する干渉縞が生
じ難い、等の利点がある。単層型感光体では、以上のよ
うな利点に加え、さらに、感光層の表面近傍で入射光の
ほとんどが吸収され、電荷が発生するので、照射光の感
光層中での拡散はほとんど無視でき、さらに帯電後の表
面電荷中和に至るまでの電荷の移動距離が積層型感光体
に比べ少ないという利点が挙げられる。このため、光お
よび電荷キャリアの拡散による画像ボケが起きづらく、
高解像度が期待できるだけでなく、感光層の膜厚をより
厚くした場合にも、電荷および入射光の拡散の度合いが
さほど変わらず、解像度もあまり低下しない。On the other hand, a single-layer type positively charged photoreceptor as described in JP-A-61-77054, JP-A-61-188543, JP-A-2-228670, JP-B-7-97223 and JP-A-7-97225 is used. In such a case, it is considered that such ozone generation is reduced as one advantage, and although it is often inferior to a negatively-charged laminated photoreceptor in terms of electrical characteristics, it is partially used in practice. . In addition to the effect on the generation of ozone, the single-layer type photoreceptor has advantages in that the number of coating steps is reduced, and that interference fringes to semiconductor laser light hardly occur. In addition to the advantages described above, the single-layer photoreceptor absorbs most of the incident light near the surface of the photosensitive layer and generates charges, so that the diffusion of irradiation light in the photosensitive layer can be almost ignored. In addition, there is an advantage that the charge transfer distance until the surface charge is neutralized after charging is smaller than that of the laminated photoreceptor. Therefore, image blur due to diffusion of light and charge carriers is less likely to occur,
In addition to expecting high resolution, even when the thickness of the photosensitive layer is increased, the degree of diffusion of charges and incident light does not change so much, and the resolution does not decrease much.
【0005】一方、積層型感光体では、基体付近で電荷
発生が起きるため、電荷輸送層中での入射光および電荷
発生層より注入された電荷キャリアの拡散が厚膜になる
につれて増大し、実質45μm以上の感光層ではかなり
の画像ボケが生じ、高解像が要求される系での実用化は
困難であった。一方、本発明に関わる表面電荷発生型の
感光体においては、45μmあるいはそれ以上の膜厚を
有する感光体が可能である。45μm以上の厚膜感光体
は、耐磨耗性を考慮した場合に、削れによる膜減りのマ
ージンが大きく、より長寿命、即ち長期間、より多数回
の電子写真プロセスへの適用が可能である。その他に
も、電子写真学会誌、第31巻、第2号、149頁、1
992年に記載のように、厚膜化により感度が向上する
メリットがある。しかし、従来の単層型感光体は、使わ
れている材料、特に電荷輸送材料が限られたものであ
り、実用化がほとんどなされなかったのが現状である。On the other hand, in the case of a stacked photoreceptor, since charge generation occurs near the substrate, the diffusion of incident light in the charge transport layer and the charge carriers injected from the charge generation layer increase as the film becomes thicker. In the case of a photosensitive layer having a thickness of 45 μm or more, considerable image blur occurs, and it has been difficult to put the photosensitive layer to practical use in a system requiring high resolution. On the other hand, in the photoconductor of the surface charge generation type according to the present invention, a photoconductor having a film thickness of 45 μm or more is possible. Thick film photoreceptors having a thickness of 45 μm or more have a large margin of film reduction due to abrasion in consideration of abrasion resistance, and have a longer life, that is, can be applied to the electrophotography process more times, that is, longer. . In addition, Journal of the Society of Electrophotography, Vol. 31, No. 2, pp. 149, 1
As described in 992, there is an advantage that the sensitivity is improved by increasing the film thickness. However, in the conventional single-layer type photoreceptor, the materials used, in particular, the charge transporting materials are limited, and practically no practical use has been made at present.
【0006】[0006]
【発明が解決しようとする課題】本発明は、このような
現状に鑑みなされたもので、高感度、高応答性を有し、
繰り返し使用時の耐久性に優れた高寿命、高耐刷な正帯
電用の単層型電子写真感光体を提供することを目的とす
るものである。SUMMARY OF THE INVENTION The present invention has been made in view of such circumstances, and has high sensitivity and high responsiveness.
It is an object of the present invention to provide a single-layer type electrophotographic photoreceptor for positive charging, which has excellent durability when repeatedly used and has a long life and high printing durability.
【0007】[0007]
【課題を解決するための手段】本発明は、上記課題を解
決するために鋭意研究を重ねた結果、導電性基体上に、
少なくとも電荷発生化合物、正孔輸送性化合物、及び電
子輸送性顔料を含む単層型感光層を有する電子写真感光
体おいて、該感光層の電荷移動度が電界強度3×105
V/cmにおいて1×105 cm2 /Vs以上となるよ
うに設定することにより上記課題が解決されることを見
いだした。このようにして得られる電子写真感光体は高
感度、高応答性を有し、さらには高寿命、高耐刷な感光
体であり、高速、高解像度が要求される電子写真方式に
最適である。Means for Solving the Problems According to the present invention, as a result of intensive studies to solve the above-mentioned problems, as a result,
In an electrophotographic photosensitive member having a single-layer photosensitive layer containing at least a charge generating compound, a hole transporting compound, and an electron transporting pigment, the charge mobility of the photosensitive layer is 3 × 10 5.
It has been found that the above problem can be solved by setting the value to be 1 × 10 5 cm 2 / Vs or more at V / cm. The electrophotographic photoreceptor thus obtained has high sensitivity and high responsiveness, and is a photoreceptor having a long life and high printing durability, and is most suitable for an electrophotographic method requiring high speed and high resolution. .
【0008】[0008]
【発明の実施の形態】以下、本発明の実施の形態につい
て詳細に説明する。本発明の層構成を図1、2に記す。
基本となる感光層が導電性支持体上に直接形成された図
1の構成と、導電性支持体と感光層との間に下引き層を
設けた図2の構成を取り得る。さらには必要に応じて、
接着層、弾性層、表面保護層等を有していてもよいこと
は言うまでもない。Embodiments of the present invention will be described below in detail. The layer structure of the present invention is shown in FIGS.
The configuration shown in FIG. 1 in which a basic photosensitive layer is directly formed on a conductive support, and the configuration shown in FIG. 2 in which an undercoat layer is provided between the conductive support and the photosensitive layer can be adopted. And if needed,
Needless to say, it may have an adhesive layer, an elastic layer, a surface protective layer, and the like.
【0009】以下、本感光体の層構成を詳細に説明す
る。感光層は導電性支持体上に積層されるが、導電性支
持体は、例えばアルミニウム、ステンレス鋼、銅、ニッ
ケル、亜鉛、インジウム、金、銀等の金属材料、ポリエ
ステル等のポリマー、紙、ガラス、等の絶縁性基体の表
面にアルミニウム、銅、パラジウム、酸化錫、酸化イン
ジウム、導電性高分子等の導電性層を設けたものが挙げ
られる。導電性支持体の表面は、画質に影響のない範囲
で各種の処理を行うことができる。例えば、表面の酸化
処理や薬品処理を行うことができる。電極酸化などによ
り、金属酸化処理した金属ドラムなどが該当する。形状
は表面切削加工済みあるいは未加工のドラム、シート、
ベルト、シームレスベルト等の任意の形状を取ることが
できる。Hereinafter, the layer constitution of the present photoreceptor will be described in detail. The photosensitive layer is laminated on a conductive support, and the conductive support includes, for example, a metal material such as aluminum, stainless steel, copper, nickel, zinc, indium, gold, and silver; a polymer such as polyester; paper; and glass. And the like, provided with a conductive layer of aluminum, copper, palladium, tin oxide, indium oxide, a conductive polymer, or the like on the surface of an insulating substrate such as. The surface of the conductive support can be subjected to various treatments within a range that does not affect the image quality. For example, surface oxidation treatment or chemical treatment can be performed. A metal drum or the like that has been subjected to a metal oxidation treatment by electrode oxidation or the like corresponds to this. The shape can be surface-cut or unprocessed drums, sheets,
Any shape such as a belt and a seamless belt can be adopted.
【0010】電荷発生化合物としてはフタロシアニン化
合物が好適である。フタロシアニン化合物は、負帯電積
層型感光体の、電荷発生層にも使用されるものの、その
膜厚は1μm以下で、膜中での電荷の滞留はほとんど問
題にならないのに対して、本発明のような単層型感光体
では、通常、その50倍以上の膜厚で用いられるので、
それ自身が電荷の移動のトラップにならないことが必要
である。また、負帯電積層型感光体中の電荷発生層の場
合と異なり、本発明のような単層型感光体では、電荷発
生材料がかなり希薄な濃度領域で使用され、しかも周り
を電荷輸送材料等が取り囲む形になっているので、周り
の材料と、電気物性面あるいは分散性、液安定性等の諸
物性面を総合的に勘案して、より相性の良い材料を選択
する必要がある。A phthalocyanine compound is preferred as the charge generating compound. Although the phthalocyanine compound is also used for the charge generation layer of the negatively charged laminated photoreceptor, the thickness of the phthalocyanine compound is 1 μm or less. Such a single-layer type photoreceptor is usually used at a film thickness of 50 times or more than that,
It is necessary that it does not itself trap electric charge. Further, unlike the case of the charge generation layer in the negatively charged laminated photoreceptor, in the single-layer type photoreceptor of the present invention, the charge generation material is used in a considerably dilute concentration region, and furthermore, the charge transporting material and the like are surrounded. , It is necessary to select a more compatible material in consideration of the surrounding materials and various physical properties such as electrical properties or dispersibility and liquid stability.
【0011】すなわち、負帯電積層型感光体の電荷発生
層として使用される材料が必ずしもそのまま単層型感光
体に使用できるだけでなく、単なる感度以外にも、たと
えば帯電性、残留電位、繰り返し安定性、膜中の分散
性、塗布液の安定性等を考慮する必要がある。そのよう
な条件に合致する化合物としてチタン、ガリウム、珪素
のうち少なくともいずれか一つの元素を中心金属として
有する各種結晶型フタロシアニン化合物が好適に使用で
きる。例えば、チタニルフタロシアニン(別称オキシチ
タニウムフタロシアニン)、中心金属のチタンに水酸基
を有する化合物を架橋させたフタロシアニン、クロロガ
リウムフタロシアニン、ヒドロキシガリウムフタロシア
ニン、ヒドロキシ珪素フタロシアニン等の各種結晶型フ
タロシアニンが挙げられる。このうち、チタニルフタロ
シアニン、ヒドロキシガリウムフタロシアニン、ヒドロ
キシ珪素フタロシアニンが好ましく、CuKα線による
X線回折図のブラッグ角2θ(±0.2゜)が9.5
°、24.1°、27.3°にピークを示す結晶型のチ
タニルフタロシアニンがより好ましい。感光層中におけ
るフタロシアニン化合物の含有量は、少な過ぎると感度
が低く、また感光層のより深い、基体側まで光が侵入し
てしまい、そこで発生した電子が排出されにくくなり、
多すぎると帯電性の低下を招くため、バインダーポリマ
ー100重量部に対して1.5重量部以上20重量部以
下、より好ましくは2重量部以上、10重量部以下含ま
れることがが好ましい。That is, the material used as the charge generation layer of the negatively charged laminated photoreceptor cannot always be used as it is for the single layer type photoreceptor. It is necessary to consider the dispersibility in the film, the stability of the coating solution, and the like. As a compound meeting such conditions, various crystalline phthalocyanine compounds having at least one element of titanium, gallium and silicon as a central metal can be suitably used. Examples thereof include various crystalline phthalocyanines such as titanyl phthalocyanine (also known as oxytitanium phthalocyanine), phthalocyanine obtained by crosslinking a compound having a hydroxyl group to titanium as a central metal, chlorogallium phthalocyanine, hydroxygallium phthalocyanine, and hydroxysilicon phthalocyanine. Among them, titanyl phthalocyanine, hydroxygallium phthalocyanine, and hydroxysilicon phthalocyanine are preferable, and the Bragg angle 2θ (± 0.2 °) of the X-ray diffraction diagram by CuKα ray is 9.5.
Crystalline titanyl phthalocyanine having peaks at °, 24.1 ° and 27.3 ° is more preferred. If the content of the phthalocyanine compound in the photosensitive layer is too small, the sensitivity is low, and light penetrates deeper into the photosensitive layer, to the substrate side, and electrons generated there are difficult to be discharged,
If the amount is too large, the chargeability is reduced. Therefore, the amount is preferably 1.5 to 20 parts by weight, more preferably 2 to 10 parts by weight, based on 100 parts by weight of the binder polymer.
【0012】正孔輸送性化合物は、上記電荷発生材料が
光を吸収して電子と正孔の電荷分離を起した後に、正孔
を輸送する役割を担う。本発明においては、感光体は単
層で正帯電方式であるので、正孔は、表面近傍で発生
し、基体まで移動することになる。また、特に高速の電
子写真プロセスを用いる系では、正孔の移動度が高いも
のを使用することが必要である。具体的には、Time
−of−Flight法等による測定で、電界強度3×
105 V/cmにおいて1×105 cm2 /Vs以上で
あることが必須である。The hole transporting compound plays a role of transporting holes after the charge generating material absorbs light to cause charge separation of electrons and holes. In the present invention, since the photoconductor is a single-layer, positive-charging system, holes are generated near the surface and move to the substrate. In particular, in a system using a high-speed electrophotographic process, it is necessary to use a material having a high hole mobility. Specifically, Time
-Of-Flight method, etc., the electric field strength 3 ×
At 10 5 V / cm, it is essential that it be 1 × 10 5 cm 2 / Vs or more.
【0013】好適な正孔輸送性化合物料例としては、ピ
ラゾリン誘導体、カルバゾール誘導体、エナミン誘導
体、オキサゾール誘導体、ヒドラゾン誘導体、スチルベ
ン誘導体、アリールアミン誘導体、ブタジエン誘導体、
オキサジアゾール誘導体、チアゾール誘導体、チアジア
ゾール誘導体、トリアゾール誘導体、イミダゾール誘導
体、イミダゾロン誘導体、イミダゾリジン誘導体、スチ
リル化合物、ベンゾチアゾール誘導体、ベンズイミダゾ
ール誘導体、アクリジン誘導体、フェナジン誘導体等の
低分子化合物が使用できる。このうち、エナミン誘導
体、ヒドラゾン誘導体、スチルベン誘導体、アリールア
ミン誘導体、ブタジエン誘導体、スチリル化合物が好ま
しい。以上の正孔輸送型電荷輸送剤は1種、または2種
以上を組み合わせて用いられる。正孔輸送性化合物の含
有量としては、特に制限はないが、バインダーポリマー
100重量部に対して通常は10重量部以上500重量
部以下、好ましくは30重量部以上150重量部以下、
さらに好ましくは40重量部以上120重量部以下であ
る。Suitable examples of the hole transporting compound include pyrazoline derivatives, carbazole derivatives, enamine derivatives, oxazole derivatives, hydrazone derivatives, stilbene derivatives, arylamine derivatives, butadiene derivatives,
Low molecular compounds such as oxadiazole derivatives, thiazole derivatives, thiadiazole derivatives, triazole derivatives, imidazole derivatives, imidazolone derivatives, imidazolidine derivatives, styryl compounds, benzothiazole derivatives, benzimidazole derivatives, acridine derivatives, and phenazine derivatives can be used. Among them, enamine derivatives, hydrazone derivatives, stilbene derivatives, arylamine derivatives, butadiene derivatives, and styryl compounds are preferred. The above hole transport type charge transport agents are used alone or in combination of two or more. The content of the hole transporting compound is not particularly limited, but is usually 10 parts by weight or more and 500 parts by weight or less, preferably 30 parts by weight or more and 150 parts by weight or less with respect to 100 parts by weight of the binder polymer.
More preferably, the amount is 40 parts by weight or more and 120 parts by weight or less.
【0014】電子輸送性顔料は、前記電荷発生材料が光
を吸収して電子と正孔の電荷分離を起した後に、電子を
輸送する役割を担う。本発明においては、感光体は単層
で正帯電方式であるので、電子は、表面近傍で発生した
後に表面まで移動し、表面電荷を打ち消す役割を担って
いる。電子の移動距離としては必ずしも長くないので、
電子の移動度は必ずしも正孔輸送剤量ほど高いことは必
要ないものの、電子が感光層中に残留したままだと続く
プロセスにおいて帯電性の低下をまねくので、十分電子
の抜けが良いものを使用することが望ましい。また、バ
インダー樹脂に非相溶の顔料であることが、相溶である
化合物よりも耐ガス性および材料選択の広さの観点から
好ましく、このような化合物としては、例えばペリレン
系化合物、アゾ系化合物、チアピリリウム塩誘導体、ピ
リリウム塩誘導体、ベンゾキノン誘導体、ナフトキノン
誘導体、アントラキノン誘導体、ジフェノキノン誘導
体、フルオレノン誘導体等が挙げられる。このうち、ペ
リレン系化合物が特に好適に用いられる。電子輸送性化
合物の含有量としては、少なすぎると電子輸送能が不足
し、多すぎると帯電性が低下するため、バインダーポリ
マー100重量部に対して、通常は0.1重量部以上5
0重量部以下、好ましくは1重量部以上25重量部以
下、さらに好ましくは2重量部以上10重量部以下であ
る。The electron transporting pigment plays a role of transporting electrons after the charge generating material absorbs light to cause charge separation of electrons and holes. In the present invention, since the photoreceptor is a single-layer, positively-charged system, electrons generate near the surface and then move to the surface to cancel the surface charge. Since the electron travel distance is not always long,
Although the electron mobility does not necessarily need to be as high as the amount of the hole transporting agent, use a material that has sufficient electron removal because it causes a decrease in chargeability in the process where electrons remain in the photosensitive layer and continues. It is desirable to do. Further, a pigment that is incompatible with the binder resin is preferable from the viewpoint of gas resistance and a wide range of material selection than a compound that is compatible with the binder resin. Examples of such a compound include a perylene compound and an azo compound. Compounds, thiapyrylium salt derivatives, pyrylium salt derivatives, benzoquinone derivatives, naphthoquinone derivatives, anthraquinone derivatives, diphenoquinone derivatives, fluorenone derivatives and the like. Of these, perylene compounds are particularly preferably used. When the content of the electron transporting compound is too small, the electron transporting ability is insufficient, and when the content is too large, the chargeability is reduced.
0 parts by weight or less, preferably 1 part by weight or more and 25 parts by weight or less, more preferably 2 parts by weight or more and 10 parts by weight or less.
【0015】感光層の膜形成に際してはバインダーポリ
マーが使用される。この場合、感光層は上記フタロシア
ニン化合物、正孔輸送性化合物、電子輸送性化合物およ
び各種添加剤とバインダーポリマーを溶剤に溶解あるい
は分散して得られる塗布液を塗布、乾燥して得ることが
できる。バインダーポリマーとしては、例えばブタジエ
ン、スチレン、酢酸ビニル、塩化ビニル、アクリル酸エ
ステル、メタクリル酸エステル、ビニルアルコール、エ
チルビニルエーテル等のビニル化合物の重合体及び共重
合体、ポリビニルブチラール、ポリビニルホルマール、
部分変性ポリビニルアセタール、ポリカーボネート、ポ
リエステル、ポリアミド、ポリウレタン、セルロースエ
ーテル、フェノキシ樹脂、ケイ素樹脂、エポキシ樹脂、
ポリ−N−ビニルカルバゾール樹脂等が挙げられる。こ
れらは適当な硬化剤等を用いて熱、光等により架橋させ
て用いる事もできる。これらのバインダーは単独で、ま
たは2種類以上を組み合わせて用いることができる。In forming the photosensitive layer, a binder polymer is used. In this case, the photosensitive layer can be obtained by applying and drying a coating solution obtained by dissolving or dispersing the phthalocyanine compound, the hole transporting compound, the electron transporting compound and various additives and a binder polymer in a solvent. As the binder polymer, for example, butadiene, styrene, vinyl acetate, vinyl chloride, acrylic acid ester, methacrylic acid ester, vinyl alcohol, polymers and copolymers of vinyl compounds such as ethyl vinyl ether, polyvinyl butyral, polyvinyl formal,
Partially modified polyvinyl acetal, polycarbonate, polyester, polyamide, polyurethane, cellulose ether, phenoxy resin, silicon resin, epoxy resin,
Poly-N-vinyl carbazole resin and the like can be mentioned. These can be used after being crosslinked by heat, light or the like using an appropriate curing agent or the like. These binders can be used alone or in combination of two or more.
【0016】感光層中には必要に応じて電子吸引性化合
物を添加しても良い。電子吸引性化合物としては、テト
ラシアノキノジメタン、ジシアノキノメタン、ジシアノ
キノビニル基を有する芳香族エステル類等のシアノ化合
物;2,4,6−トリニトロフルオレノン等のニトロ化
合物;ペリレン等の縮合多環芳香族化合物;ジフェノキ
ノン誘導体;キノン類;アルデヒド類;ケトン類;エス
テル類;酸無水物;フタリド類;置換及び無置換サリチ
ル酸の金属錯体;置換及び無置換サリチル酸の金属塩;
芳香族カルボン酸の金属錯体;芳香族カルボン酸の金属
塩が挙げられる。好ましくは、シアノ化合物、ニトロ化
合物、縮合多環芳香族化合物、ジフェノキノン誘導体、
置換及び無置換サリチル酸の金属錯体、置換及び無置換
サリチル酸の金属塩;芳香族カルボン酸の金属錯体;芳
香族カルボン酸の金属塩を用いるのがよい。An electron-withdrawing compound may be added to the photosensitive layer if necessary. Examples of the electron-withdrawing compound include cyano compounds such as tetracyanoquinodimethane, dicyanoquinomethane, and aromatic esters having a dicyanoquinovinyl group; nitro compounds such as 2,4,6-trinitrofluorenone; and condensation of perylene and the like. Polycyclic aromatic compounds; diphenoquinone derivatives; quinones; aldehydes; ketones; esters; acid anhydrides; phthalides; substituted and unsubstituted salicylic acid metal complexes; substituted and unsubstituted salicylic acid metal salts;
Metal complexes of aromatic carboxylic acids; metal salts of aromatic carboxylic acids. Preferably, a cyano compound, a nitro compound, a condensed polycyclic aromatic compound, a diphenoquinone derivative,
It is preferable to use substituted and unsubstituted metal complexes of salicylic acid, substituted and unsubstituted metal salts of salicylic acid, metal complexes of aromatic carboxylic acids, and metal salts of aromatic carboxylic acids.
【0017】更に、上記感光層は成膜性、可とう性、塗
布性機械的強度、製膜性、耐久性等を向上させるために
周知の可塑剤、酸化防止剤、紫外線吸収剤、レベリング
剤を含有していてもよい。感光層の膜厚は、好ましくは
45μm以上、より好ましくは50μm以上である。本
発明の感光体は、積層型感光体に比べて、感光層を厚く
することできる。感光層形成のための塗布液作製に際し
ては、フタロシアニン化合物、正孔輸送性化合物、電子
輸送性化合物、バインダーポリマー等の組成物を別々に
乾式、あるいは適当な溶媒中で分散/溶解した後に混合
する方法、あるいは、組成物のうち2種以上を一緒に分
散あるいは溶解した後に混合する等の方法が適宜用いら
れる。Further, the above-mentioned photosensitive layer is a well-known plasticizer, antioxidant, ultraviolet absorber, leveling agent for improving film forming property, flexibility, coating property, mechanical strength, film forming property, durability and the like. May be contained. The thickness of the photosensitive layer is preferably at least 45 μm, more preferably at least 50 μm. The photoreceptor of the present invention can have a thicker photosensitive layer than a laminated photoreceptor. In preparing a coating solution for forming a photosensitive layer, compositions such as a phthalocyanine compound, a hole transporting compound, an electron transporting compound, and a binder polymer are mixed separately after being dispersed / dissolved in a dry system or an appropriate solvent. A method, or a method in which two or more of the compositions are dispersed or dissolved together and then mixed and the like are used as appropriate.
【0018】分散には通常ボールミル、超音波分散器、
ペイントシェイカー、アトライター、サンドグラインダ
等を使用する。分散、あるいは溶解に用いる溶媒として
は、ブチルアミン、ジエチルアミン、エチレンジアミ
ン、イソプロパノールアミン、トリエタノールアミン、
トリエチレンジアミン、N,N−ジメチルホルムアミ
ド、アセトン、メチルエチルケトン、シクロヘキサノ
ン、ベンゼン、トルエン、キシレン、クロロホルム、
1,2ージクロルエタン、1,2ージクロルプロパン、
1,1,2−トリクロルエタン、1,1,1−トリクロ
ルエタン、トリクロルエチレン、テトラクロルエタン、
ジクロルメタン、テトラヒドロフラン、ジオキサン、メ
チルアルコール、エチルアルコール、イソプロピルアル
コール、ジメチルグリコール、酢酸エチル、酢酸ブチ
ル、ジメチルスルホキシド、メチルセルソルブ、等が挙
げられる。これらの分散媒は、1種単独で使用してもよ
く、或いは2種以上を混合溶媒として用いても良い。こ
の塗布液をディッピング法、リングコート法、スプレー
法、バーコーター法、ブレード法、ロールコーター法、
ワイヤーバー塗工法、ナイフコーター塗工法、等の塗布
法により塗布後、乾燥する。このうち、45μm以上の
厚膜塗布方法としてはスプレー法が特に好適に用いられ
る。本感光体は必要に応じて、下引き層、透明絶縁層、
表面保護層等を有していてもよいことは言うまでもな
い。For dispersion, a ball mill, an ultrasonic disperser,
Use a paint shaker, attritor, sand grinder, etc. As a solvent used for dispersion or dissolution, butylamine, diethylamine, ethylenediamine, isopropanolamine, triethanolamine,
Triethylenediamine, N, N-dimethylformamide, acetone, methyl ethyl ketone, cyclohexanone, benzene, toluene, xylene, chloroform,
1,2-dichloroethane, 1,2-dichloropropane,
1,1,2-trichloroethane, 1,1,1-trichloroethane, trichloroethylene, tetrachloroethane,
Examples include dichloromethane, tetrahydrofuran, dioxane, methyl alcohol, ethyl alcohol, isopropyl alcohol, dimethyl glycol, ethyl acetate, butyl acetate, dimethyl sulfoxide, and methyl cellosolve. One of these dispersion media may be used alone, or two or more thereof may be used as a mixed solvent. This coating solution is dipped, ring-coated, sprayed, bar-coated, bladed, roll-coated,
The coating is performed by a coating method such as a wire bar coating method or a knife coater coating method, and then dried. Among them, a spray method is particularly preferably used as a method for coating a thick film having a thickness of 45 μm or more. The photoreceptor may have an undercoat layer, a transparent insulating layer,
Needless to say, a surface protective layer or the like may be provided.
【0019】下引き層は通常、感光層と導電性支持体の
間に使用され、通常使用される公知のものが使用でき
る。下引き層としては酸化チタン、酸化アルミニウム、
ジルコニア、酸化珪素などの無機微粒子、有機顔料およ
び架橋ポリマー等の有機微粒子、ポリアミド樹脂、フェ
ノール樹脂、メラミン樹脂、カゼイン、ポリウレタン樹
脂、エポキシ樹脂、セルロース、ニトロセルロース、ポ
リビニルアルコール、ポリビニルブチラールなどの樹脂
等の成分を使用することができる。これらの微粒子、樹
脂は単独でまたは2種以上を混合してしようできる、厚
さは、通常0.01〜50μm 、好ましくは0.01〜
10μmである。The undercoat layer is usually used between the photosensitive layer and the conductive support, and a commonly used known layer can be used. Titanium oxide, aluminum oxide,
Inorganic fine particles such as zirconia and silicon oxide, organic fine particles such as organic pigments and crosslinked polymers, polyamide resins, phenolic resins, melamine resins, caseins, polyurethane resins, epoxy resins, resins such as cellulose, nitrocellulose, polyvinyl alcohol, polyvinyl butyral, etc. Can be used. These fine particles and resin can be used alone or as a mixture of two or more kinds. The thickness is usually 0.01 to 50 μm, preferably 0.01 to 50 μm.
10 μm.
【0020】本発明の感光体に表面保護層を設ける場
合、保護層の厚みは0.01〜20μmが可能であり、
好ましくは0.1〜10μmである。保護層には前記の
バインダーを用いることができるが、前記の電荷発生
剤、電荷輸送剤、添加剤、金属、金属酸化物などの導電
材料、滑剤等を含有しても良い。本発明の電子写真感光
体を使用するのにあたって、帯電器はコロトロン、スコ
ロトロンなどのコロナ帯電器、帯電ローラー、帯電プラ
シ等の接触帯電器などが用いられる。露光はハロゲンラ
ンプ、蛍光灯、レーザー(半導体、He−Ne)、LE
D、感光体内部露光方式等が用いられるが、デジタル式
電子写真方式として、レーザー、LED、光シャッター
アレイ等を用いることが好ましい。現像行程はカスケー
ド現像、一成分絶縁トナー現像、一成分導電トナー現
像、二成分磁気ブラシ現像などの乾式現像方式や湿式現
像方式などが用いられる。転写行程はコロナ転写、ロー
ラー転写、ベルト転写などの静電転写法、圧力転写法、
粘着転写法が用いられる。定着は熱ローラ定着、フラッ
シュ定着、オーブン定着、圧力定着などが用いられる。
クリーニングにはブラシクリーナー、磁気ブラシクリー
ナー、静電ブラシクリーナー、磁気ローラークリーナ
ー、ブレードクリーナー、などが用いられる。上記のよ
うにして得られた本発明の電子写真感光体は、従来の感
光体に比べ、高感度、高応答でかつ高耐刷であり、より
高速かつ高寿命の要求される複写機、プリンター、ファ
ックス、製版機等の電子写真分野に好適である。When a surface protective layer is provided on the photoreceptor of the present invention, the protective layer can have a thickness of 0.01 to 20 μm,
Preferably it is 0.1 to 10 μm. The above-mentioned binder can be used for the protective layer, and the protective layer may contain the above-mentioned charge generating agent, charge transporting agent, additive, conductive material such as metal and metal oxide, and lubricant. In using the electrophotographic photoreceptor of the present invention, a corona charger such as a corotron and a scorotron, and a contact charger such as a charging roller and a charging brush are used. Exposure: halogen lamp, fluorescent lamp, laser (semiconductor, He-Ne), LE
D, a photoreceptor internal exposure system and the like are used, but as a digital electrophotographic system, it is preferable to use a laser, an LED, an optical shutter array or the like. In the development process, a dry development method such as cascade development, one-component insulated toner development, one-component conductive toner development, and two-component magnetic brush development, a wet development method, and the like are used. The transfer process includes electrostatic transfer methods such as corona transfer, roller transfer, and belt transfer, pressure transfer methods,
An adhesive transfer method is used. For fixing, heat roller fixing, flash fixing, oven fixing, pressure fixing and the like are used.
For cleaning, a brush cleaner, a magnetic brush cleaner, an electrostatic brush cleaner, a magnetic roller cleaner, a blade cleaner, and the like are used. The electrophotographic photoreceptor of the present invention obtained as described above has a higher sensitivity, a higher response, a higher printing durability, and a higher speed and longer life than a conventional photoreceptor. , Fax machine, plate making machine and the like.
【0021】[0021]
【実施例】以下、本発明を実施例により具体的に説明す
る。しかしながら、本発明は以下の実施例に限定される
ものではない。なお、下記記載中、「部」は「重量部」
を表す。 (実施例1)図3に示すCuKα線による粉末X線回折
パターンを有するオキシチタニウムフタロシアニン3部
および下記構造式のペリレン顔料8部をトルエン180
部に加え、サンドグラインダーにより分散し、顔料分散
液を得た。一方、下記表1中の正孔輸送材料1を70重
量部、ポリカーボネート樹脂100部をトルエン420
部に溶解し、これに上記の分散液を、ホモジナイザーに
より均一になるように混合した。このように調整した塗
布液を、支持体として、アルミニウム蒸着層を有する膜
厚75μmのポリエステルフィルム上に、乾燥膜厚が5
8〜59μmになるように塗布し、単層型の電子写真感
光体を得た。The present invention will be described below in more detail with reference to examples. However, the present invention is not limited to the following examples. In the following description, “parts” means “parts by weight”.
Represents Example 1 3 parts of oxytitanium phthalocyanine having a powder X-ray diffraction pattern by CuKα radiation shown in FIG. 3 and 8 parts of a perylene pigment having the following structural formula were mixed with toluene 180
Of the mixture, and dispersed by a sand grinder to obtain a pigment dispersion. On the other hand, 70 parts by weight of the hole transport material 1 and 100 parts of the polycarbonate resin in
And the above dispersion was mixed with a homogenizer so as to be uniform. The coating solution thus adjusted was applied as a support on a 75 μm-thick polyester film having an aluminum vapor-deposited layer to a dry film thickness of 5 μm.
The coating was performed so as to have a thickness of 8 to 59 μm to obtain a single-layer type electrophotographic photosensitive member.
【0022】[0022]
【化1】 Embedded image
【0023】(実施例2)正孔輸送材料を表1中の化合
物1に代えて化合物2を使用した以外はすべて実施例1
と同様の方法で電子写真感光体を得た。 (比較例1、2)実施例1において正孔輸送材料を表1
中の化合物1に代えて化合物3、4を使用した以外はす
べて実施例1と同様の方法で電子写真感光体体を得た。 (参考例1、2)実施例1、2において膜厚を29μm
にした以外は全て同じ方法で電子写真感光体を得た。Example 2 Example 1 was repeated except that Compound 2 was used in place of Compound 1 in Table 1 for the hole transporting material.
An electrophotographic photoreceptor was obtained in the same manner as described above. (Comparative Examples 1 and 2) Table 1 shows the hole transport materials in Example 1.
An electrophotographic photoreceptor was obtained in the same manner as in Example 1 except that Compounds 3 and 4 were used in place of Compound 1. (Reference Examples 1 and 2) In Examples 1 and 2, the film thickness was 29 μm.
An electrophotographic photoreceptor was obtained in the same manner except for the above.
【0024】[0024]
【表1】 [Table 1]
【0025】<感光体の評価>電子写真学会測定標準に
従って作製された測定装置(続電子写真技術の基礎と応
用、電子写真学会編、コロナ社、404−405頁記
載)を使用し、上記感光体をアルミニウム製ドラムに貼
り付けて円筒状にし、アルミニウム製ドラムと感光体の
アルミニウム基体との導通を取り、帯電、露光、電位測
定、除電のサイクルによる電気特性評価試験を行った。
その再、初期表面電位を700Vとし、露光は780n
m、除電は660nmの単色光とした。評価項目として
は、表面電位が700Vから350Vに半減するのに要
した露光量(半減露光量、E1/2 )、および780nm
の光を1.4μJ/cm2 照射した時点の表面電位(V
L)を測定した。VL測定に際しては、露光−電位測定
に要する時間について100msおよび200msの2
点で行った。結果を表2に示す。100msでのVL値
が低ければ高速プロセスにも対応できることを示し、1
00msではVL値が高くても200msで小さけれ
ば、およそ中速〜低速プロセスでなら使用できることを
示す。一方、200msでもVL値が小さくならない場
合、使用した正孔輸送材料は本発明の45μm以上の厚
膜感光体には不適当であることを示す。<Evaluation of Photoreceptor> The above photosensitivity was measured using a measuring apparatus (basic and application of electrophotographic technology, edited by the Electrophotographic Society, Corona Co., pp. 404-405) manufactured according to the electrophotographic society measurement standard. The body was affixed to an aluminum drum to form a cylinder, and conduction between the aluminum drum and the aluminum substrate of the photoreceptor was established. An electrical property evaluation test was performed by a cycle of charging, exposure, potential measurement, and static elimination.
Again, the initial surface potential was set to 700 V, and the exposure was 780 n
m, and neutralization was monochromatic light of 660 nm. The evaluation items include an exposure amount required to reduce the surface potential by half from 700 V to 350 V (half exposure amount, E 1/2 ), and 780 nm.
Surface light (V) at the time of irradiation of 1.4 μJ / cm 2 of
L) was measured. In the VL measurement, the time required for the exposure-potential measurement was 100 ms and 200 ms.
Went in point. Table 2 shows the results. If the VL value at 100 ms is low, it is possible to cope with a high-speed process.
In the case of 00 ms, if the VL value is high and the VL value is small in 200 ms, it can be used in a medium to low speed process. On the other hand, if the VL value does not decrease even after 200 ms, it indicates that the used hole transport material is not suitable for the thick film photoreceptor of the present invention having a thickness of 45 μm or more.
【0026】[0026]
【表2】 [Table 2]
【0027】(実施例3)支持体として、円筒状のアル
ミニウム製ドラム(直径30mm、長さ247mm)を
使用し、実施例1記載の方法と同様に塗布液を調整し、
浸せき塗布により膜厚50μmの電子写真感光体ドラム
を作製した。このドラムをブラザー工業製レーザープリ
ンターHL−1040に装填し、印刷テストを行ったと
ころ、画像ボケ等の無い良好な画像が得られ、しかも一
枚間欠モードで1万枚印刷後も膜削れは5μ程度と初期
膜厚の10%程度と小さく、画像にほとんど変化は見ら
れなかった。(Example 3) A cylindrical aluminum drum (diameter 30 mm, length 247 mm) was used as a support, and a coating solution was prepared in the same manner as in Example 1.
An electrophotographic photosensitive drum having a thickness of 50 μm was prepared by immersion coating. This drum was loaded into a Brother Industrial Laser Printer HL-1040 and a printing test was performed. As a result, a good image without image blur was obtained. Further, even after printing 10,000 sheets in the single-sheet intermittent mode, film scraping was 5 μm. The degree was as small as about 10% of the initial film thickness, and almost no change was observed in the image.
【0028】(実施例4)図3に示すCuKα線による
粉末X線スペクトルパターンを有するオキシチタニウム
フタロシアニン3部および実施例1記載の構造式のペリ
レン顔料8部をキシレン154部に加え、サンドグライ
ンダーにより分散した後、キシレン55部で希釈し、分
散液を得た。一方、下記表1中の正孔輸送材料1を40
重量部、ポリカーボネート樹脂100部をキシレン20
20部に溶解し、これに上記の分散液を、ホモジナイザ
ーにより均一になるように混合して塗布液を作製した。
この塗布液を、スプレー塗布法により、アルミニウム製
ドラム(直径78mm、長さ350mm)上に、感光層
の膜厚が45μmとなるように塗布し、感光体ドラムを
作製した。この感光体ドラムを三田工業製DC−409
0に搭載し、画像試験を行ったところ、画像ボケ等の無
い良好な画像が得られた。Example 4 3 parts of oxytitanium phthalocyanine having a powder X-ray spectrum pattern by CuKα ray shown in FIG. 3 and 8 parts of a perylene pigment of the structural formula described in Example 1 were added to 154 parts of xylene, and were subjected to sand grinder. After dispersion, the mixture was diluted with 55 parts of xylene to obtain a dispersion. On the other hand, the hole transporting material 1 in
Parts by weight, 100 parts of polycarbonate resin in xylene 20
The resulting dispersion was dissolved in 20 parts, and the above dispersion was uniformly mixed with a homogenizer to prepare a coating solution.
This coating solution was applied by a spray coating method onto an aluminum drum (diameter: 78 mm, length: 350 mm) so that the thickness of the photosensitive layer was 45 μm, thereby producing a photosensitive drum. This photoreceptor drum was manufactured by DC-409 manufactured by Mita Kogyo.
0, and an image test was carried out. As a result, a good image free of image blur and the like was obtained.
【0029】(比較例3)膜厚を24μmにした以外は
全て実施例3と同様に感光体ドラムを作製し、画像試験
を行ったところ、一枚間欠モード1万枚印刷時で膜削れ
は約5μと、初期膜厚の21%程度が減ったことにな
り、画像には、線太りや像濃化が見られた。また、感光
体寿命も、実施例4に比べ、半分以下であると推定され
た。(Comparative Example 3) A photosensitive drum was prepared and an image test was performed in the same manner as in Example 3 except that the film thickness was changed to 24 μm. This means that the initial film thickness was reduced to about 5 μm, which was about 21% of the initial film thickness. In addition, the life of the photoconductor was estimated to be less than half that of Example 4.
【0030】[0030]
【発明の効果】以上説明したように、本発明により、高
感度、高応答で繰り返し安定性、耐刷性に優れ、高寿命
の正帯電用の単層型電子写真感光体が提供される。本発
明の電子写真感光体はデジタル式電子写真複写機やレー
ザープリンター、ファックスに効果的に使用されるが、
さらに電子写真技術を利用した各種製版システム、軽印
刷機等にも適用できる。As described above, according to the present invention, there is provided a single-layer type electrophotographic photoreceptor for positive charging, which has high sensitivity, high response, excellent repetition stability and printing durability, and has a long service life. The electrophotographic photoreceptor of the present invention is effectively used for digital electrophotographic copying machines, laser printers, and fax machines,
Further, the present invention can be applied to various plate making systems and light printing presses using electrophotographic technology.
【図1】本発明の電子写真感光体の概略断面図である。FIG. 1 is a schematic sectional view of an electrophotographic photosensitive member of the present invention.
【図2】本発明の電子写真感光体の別の態様の概略断面
図である。FIG. 2 is a schematic sectional view of another embodiment of the electrophotographic photosensitive member of the present invention.
【図3】実施例1で用いたオキシチタニウムフタロシア
ニンの粉末X線回折図である。FIG. 3 is a powder X-ray diffraction diagram of oxytitanium phthalocyanine used in Example 1.
1 導電性支持体、 2 感光層、 3 下引き層 1 conductive support, 2 photosensitive layer, 3 undercoat layer
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 2H068 AA14 AA19 AA20 AA28 AA31 BA12 BA14 BA15 BA33 BA36 BA37 BA38 BA39 BA41 EA17 FC02 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 2H068 AA14 AA19 AA20 AA28 AA31 BA12 BA14 BA15 BA33 BA36 BA37 BA38 BA39 BA41 EA17 FC02
Claims (8)
合物、正孔輸送性化合物及び電子輸送性顔料を含む単層
型感光層を有する電子写真感光体おいて、該感光層の正
孔移動度が電界強度3×105 V/cmにおいて1×1
05 cm2 /Vs以上であることを特徴とする正帯電型
電子写真感光体。1. An electrophotographic photosensitive member having a single-layer photosensitive layer containing at least a charge generating compound, a hole transporting compound and an electron transporting pigment on a conductive substrate. Is 1 × 1 at an electric field strength of 3 × 10 5 V / cm.
0. 5 cm 2 / Vs or more.
を特徴とする請求項1に記載の正帯電型電子写真感光
体。2. The positively charged electrophotographic photosensitive member according to claim 1, wherein the thickness of the photosensitive layer is 45 μm or more.
アゾ系化合物、チアピリリウム塩誘導体、ベンゾキノン
誘導体、ナフトキノン誘導体、アントラキノン誘導体、
ジフェノキノン誘導体及びフルオレノン誘導体からなる
群から選ばれた1種または2種を以上であることを特徴
とする請求項1又は2に記載の正帯電型電子写真感光
体。3. The method according to claim 1, wherein the electron transporting pigment is a perylene compound,
Azo compounds, thiapyrylium salt derivatives, benzoquinone derivatives, naphthoquinone derivatives, anthraquinone derivatives,
The positively chargeable electrophotographic photoreceptor according to claim 1, wherein the photoreceptor is at least one member selected from the group consisting of a diphenoquinone derivative and a fluorenone derivative.
ることを特徴とする請求項1又は2に記載の電子写真感
光体。4. The electrophotographic photosensitive member according to claim 1, wherein the electron transporting pigment is a perylene compound.
物である請求項1〜4のいずれかに記載の電子写真感光
体。5. The electrophotographic photosensitive member according to claim 1, wherein the charge generating compound is a phthalocyanine compound.
によるX線回折図のブラッグ角2θ(±0.2゜)が
9.5°、24.1°、27.3°にピークを示す結晶
型のチタニルフタロシアニンである請求項5に記載の電
子写真感光体。6. A phthalocyanine-based compound having a crystal form that shows peaks at Bragg angles 2θ (± 0.2 °) of 9.5 °, 24.1 ° and 27.3 ° in an X-ray diffraction pattern by CuKα ray. The electrophotographic photosensitive member according to claim 5, which is titanyl phthalocyanine.
00重量部に対して1.5重量部以上20重量部以下含
有されることを特徴とする請求項1〜6のいずれかに記
載の電子写真感光体。7. The charge-generating compound is a binder-polymer 1.
The electrophotographic photoreceptor according to any one of claims 1 to 6, wherein the content is 1.5 to 20 parts by weight based on 00 parts by weight.
ることを特徴とする請求項1〜7のいずれかに記載の電
子写真感光体を製造する方法。8. The method for producing an electrophotographic photosensitive member according to claim 1, wherein the photosensitive layer is formed by a spray coating method.
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JP32630299A JP2001142237A (en) | 1999-11-17 | 1999-11-17 | Electrophotographic photoreceptor |
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ID=18186258
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004354575A (en) * | 2003-05-28 | 2004-12-16 | Konica Minolta Business Technologies Inc | Electrophotographic photoreceptor, image forming method and image forming apparatus |
KR100811393B1 (en) * | 2001-12-04 | 2008-03-07 | 주식회사 하이닉스반도체 | Photoresist additive for improving pattern collapse and photoresist composition containing same |
JP2013050559A (en) * | 2011-08-30 | 2013-03-14 | Kyocera Document Solutions Inc | Positively-charged single-layered electrophotographic photoreceptor, and image forming apparatus |
JP2015175909A (en) * | 2014-03-13 | 2015-10-05 | 富士ゼロックス株式会社 | Electrophotographic photoreceptor, process cartridge, and image forming apparatus |
-
1999
- 1999-11-17 JP JP32630299A patent/JP2001142237A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100811393B1 (en) * | 2001-12-04 | 2008-03-07 | 주식회사 하이닉스반도체 | Photoresist additive for improving pattern collapse and photoresist composition containing same |
JP2004354575A (en) * | 2003-05-28 | 2004-12-16 | Konica Minolta Business Technologies Inc | Electrophotographic photoreceptor, image forming method and image forming apparatus |
JP2013050559A (en) * | 2011-08-30 | 2013-03-14 | Kyocera Document Solutions Inc | Positively-charged single-layered electrophotographic photoreceptor, and image forming apparatus |
JP2015175909A (en) * | 2014-03-13 | 2015-10-05 | 富士ゼロックス株式会社 | Electrophotographic photoreceptor, process cartridge, and image forming apparatus |
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