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JPS6348562A - Electrophotographic sensitive body - Google Patents

Electrophotographic sensitive body

Info

Publication number
JPS6348562A
JPS6348562A JP19242086A JP19242086A JPS6348562A JP S6348562 A JPS6348562 A JP S6348562A JP 19242086 A JP19242086 A JP 19242086A JP 19242086 A JP19242086 A JP 19242086A JP S6348562 A JPS6348562 A JP S6348562A
Authority
JP
Japan
Prior art keywords
transparent conductive
layer
silane coupling
substance
organic photoconductive
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
JP19242086A
Other languages
Japanese (ja)
Inventor
Tsutomu Otake
大竹 勉
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.)
Seiko Epson Corp
Original Assignee
Seiko Epson Corp
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 Seiko Epson Corp filed Critical Seiko Epson Corp
Priority to JP19242086A priority Critical patent/JPS6348562A/en
Publication of JPS6348562A publication Critical patent/JPS6348562A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/14Inert intermediate or cover layers for charge-receiving layers
    • G03G5/142Inert intermediate layers

Landscapes

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

Abstract

PURPOSE:To obtain the titled body having an improved sticking property against a substrate body, without reducing the electrophotographic characteristics by interposing a layer contg. a silane coupling material between an org. photoconductive substance and a transparent conductive substance. CONSTITUTION:An electric charge generating layer and an electric charge transfer layer are formed by effecting a gravure of the silane coupling material on one surface of the transparent conductive substance mounted on a substrate body, followed by drying it with a hot air, an subsequently, by coating the transparent conductive layer with the org. photoconductive substance, namely the electrophotographic sensitive material. Thus, the titled body which has improved sticking property against the substrate, and does not hardly reduce photosensitivity is obtd.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、暗抵抗と光感度を低下させることなく、導電
性支持体との優れた密着性を有する電子写真感光体に関
する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an electrophotographic photoreceptor that has excellent adhesion to a conductive support without reducing dark resistance and photosensitivity.

〔従来の技術〕[Conventional technology]

従来、電子写真感光体材料としては、無機及び有機光導
電性物質として多くの物質が知られている。
Conventionally, many materials are known as inorganic and organic photoconductive materials as electrophotographic photoreceptor materials.

酸化亜鉛、セレン、あるいは、硫化カドミウムなどの年
債光導電体は、光感度に関しては優れた性質を有するが
、透明性、軽量性、可撓性、公害性に問題がある。
Photoconductors such as zinc oxide, selenium, or cadmium sulfide have excellent properties in terms of photosensitivity, but have problems in transparency, lightness, flexibility, and pollution resistance.

これに対し、有機光導電性物質は、無機物質に較べて、
けるかに多くの物質が知られており、低分子型有機光導
電性物質としては、例えば、各峨金)4フクロシアニン
、無金属フタロンアニン、オキサジアゾール誘導体、ベ
ンズイミダゾールLり導体などか、また、高分子型有機
光導電性物ぽとしては、例えば、特公昭42−1867
4号公報。
On the other hand, organic photoconductive materials, compared to inorganic materials,
A large number of substances are known, and examples of low-molecular organic photoconductive substances include 4-fucrocyanine, metal-free phthalonanine, oxadiazole derivatives, benzimidazole L-conductor, etc. In addition, as a polymer type organic photoconductive material, for example, Japanese Patent Publication No. 42-1867
Publication No. 4.

特公昭42−25230号公報などにおいて開示された
、カルバゾール環のような複索環、あるいは、ナフタレ
ン環、アントラセン環のような多核芳香環を含むポリマ
ーなどが知られている。
Polymers containing polycyclic rings such as carbazole rings or polynuclear aromatic rings such as naphthalene rings and anthracene rings are known, as disclosed in Japanese Patent Publication No. 42-25230.

〔発明の解決しようとする問題点〕[Problem to be solved by the invention]

これらの有機光導電性物質は有機物質の本質的な特性と
して、占明性、軽斂性、無公害性に優れているが、無機
物質より光感度が著しく低く、また物理的性質に関して
、さらに改善されるべき点が多いため、今EI″1で、
無機光導電性物質に較べ、実用性で劣るものであった。
These organic photoconductive materials have excellent properties such as occupancy, lightness, and non-polluting properties as organic materials, but they have significantly lower photosensitivity than inorganic materials, and they also have poor physical properties. There are many points that need to be improved, so the current EI is ``1''.
Compared to inorganic photoconductive materials, it was inferior in practicality.

このうち、前者の光感度については、有機合成技術の進
歩などにより、有用な有機光導電性物質、及び、増感剤
が開示され、R躍的にそり実用価値が高まってきたが、
後者の物理的性質については問題が多く、有機光導電性
物質の実用化に大きな障害となっている。例えば、高分
子型有機光導@法物質は分子rI!J凝集力が強く、シ
ばしば結晶化を起こし透明性を損うと共に一般に固く脆
弱であり、また、支持体に対する′g着力に乏しいなど
の欠点を有する。低分子型有機光導電性物質では、感光
層を形成する方法として、蒸着、あるいは、樹脂中への
分散な≠し溶解などが用いられているが、蒸着の場合、
可撓性、支持体とので1性、さらには、感光層形成時の
効率、コストに問題があり、rJ[Il\の分散ないし
溶解の場合、可撓性、支持体との密着性は1バインダー
である樹脂の性質でほぼ決まるが、現在までに用いられ
ている樹脂では、可撓性、支持体との密着性共、充分と
は言えず、また、これらの特性が良好であっても、表面
電位の低下、光感度の低下など、望まれる電子写真特性
を損なう効果を附随し、゛満足できる結果を与えるもの
ではなかった。
Regarding the former, photosensitivity, advances in organic synthesis technology have led to the disclosure of useful organic photoconductive substances and sensitizers, and their practical value has increased dramatically.
There are many problems regarding the physical properties of the latter, which poses a major obstacle to the practical application of organic photoconductive materials. For example, polymer-type organic photoconductive@method materials have molecules rI! It has a strong J cohesive force, often causes crystallization and impairs transparency, is generally hard and brittle, and has drawbacks such as poor adhesion to a support. For low-molecular-weight organic photoconductive substances, vapor deposition or dispersion or dissolution in a resin is used as a method of forming a photosensitive layer, but in the case of vapor deposition,
There are problems with flexibility and adhesion with the support, as well as efficiency and cost during photosensitive layer formation, and when dispersing or dissolving rJ[Il This is mostly determined by the properties of the resin that is the binder, but the resins currently used cannot be said to have sufficient flexibility or adhesion to the support, and even if these properties are good, However, it has been accompanied by effects that impair desired electrophotographic properties, such as a decrease in surface potential and a decrease in photosensitivity, and thus has not been able to provide satisfactory results.

本発明は、上記のような問題点を解決するもので、その
目的とするところは、電子写真緒特性を低下させること
なく、支持体との優れた密着性を有する電子写真感光体
を提供するところにある。
The present invention is intended to solve the above-mentioned problems, and its purpose is to provide an electrophotographic photoreceptor that has excellent adhesion to a support without degrading electrophotographic properties. There it is.

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

本発明は、有機光導電性物質、透明導電性物質、および
、6明支持体より成る電子写真感光体において、有機光
導電性物質と6明導電性物質との間にシランカップリン
グ材の層を形成したことを特徴とする。
The present invention provides an electrophotographic photoreceptor comprising an organic photoconductive material, a transparent conductive material, and a 6-light support, in which a layer of a silane coupling material is provided between the organic photoconductive material and the 6-light conductive material. It is characterized by the formation of

〔実施例〕〔Example〕

インジウム酸化錫の透明溝tJi(以下、工TO)を片
面につけたホ“リエステルフィルム(ハイビーム100
L−BKO2、東し)を電子写真感光体の支持体として
用いる。
Polyester film (high beam 100
LBKO2, Toshi) is used as a support for an electrophotographic photoreceptor.

この支持体のITo上にシランカップリング剤をグラビ
ア印刷する。グラビアロールの版は150〜20.Jl
lメッンーで、シランカップリング剤は、真径50〜1
00 /J mのドツトとして工To上に印刷される。
A silane coupling agent is gravure printed on the ITo support. Gravure roll version costs 150-20. Jl
The silane coupling agent has a diameter of 50 to 1
00/J m dots are printed on the To.

転写されたシランカップリング剤を熱風乾燥させた上に
、有機光導電性物質、すなわち電子写真感光材料を塗工
する。
The transferred silane coupling agent is dried with hot air, and then an organic photoconductive substance, that is, an electrophotographic photosensitive material is applied.

を子写′A感光材料は次のようにして、作製した。銅フ
タロシアニン(Sumitone 、 0yanine
 BlueLBGN、住友化学)3r11ポリエステル
樹脂(バイロン200.東洋紡)を22゜ポリイソシア
ネート(日二写ポリウレタン)1り、メチルエチルケト
ン(以下、MFiK)/トルエン(=1/1 )70P
を混合し、ボールミルで24時間分散し、こCをA液と
する。
The photographic material 'A' was prepared as follows. Copper phthalocyanine (Sumitone, Oyanine
BlueLBGN, Sumitomo Chemical) 3r11 polyester resin (Byron 200. Toyobo), 22° polyisocyanate (Hijisha Polyurethane), methyl ethyl ketone (hereinafter referred to as MFiK)/toluene (=1/1) 70P
were mixed and dispersed in a ball mill for 24 hours, and this was used as liquid A.

また、ポリカーボネー) (N OV A RE X 
、三菱化成)27.ジンエニルヒドラゾンお導体(CT
C!−256,並用香料産業)22をテトラヒドロフラ
ン(以下THF)10yに溶解し、これをB液とする。
Also, polycarbonate) (NOV ARE
, Mitsubishi Kasei)27. Zinenylhydrazone conductor (CT
C! -256, General Perfume Sangyo) 22 was dissolved in 10y of tetrahydrofuran (hereinafter referred to as THF), and this was used as liquid B.

上述のシランカップリング剤を印刷した支持体表面上に
A液をコータで塗工して、熱風乾燥し、厚さ約1μm 
O) ′wL荷発生層を作製する。さらに、B液を塗工
し、同様に熱風乾燥し、2071 m O)電荷移動層
を作a!!!する。こうしてできた電子写真感光体を試
料1とする。
The above-mentioned silane coupling agent was printed on the surface of the support by applying liquid A using a coater, and drying with hot air to a thickness of about 1 μm.
O) Create a 'wL charge generation layer. Furthermore, liquid B was applied and dried in the same manner with hot air to form a 2071 m O) charge transfer layer a! ! ! do. The electrophotographic photoreceptor thus produced is referred to as Sample 1.

一方、比較の為、シリコンカップリング材の層を設けな
いで、r!!明4電層上にA液とB液を端層して塗工し
たものを作製し、試料2とした。
On the other hand, for comparison, without providing a layer of silicone coupling material, r! ! A sample 2 was prepared by applying liquid A and liquid B as end layers on the bright four-electrode layer.

試料1と試料2かも、密着性評価用のサン1〃を、そn
ぞれ20個ずつ作り、クロスカット試験器により密着性
の69価試験3行なった。七の禾占果を表1に示j。
Sample 1 and Sample 2 were also coated with Sun 1 for adhesion evaluation.
Twenty pieces of each were made, and three 69-valent adhesion tests were conducted using a cross-cut tester. Table 1 shows the fortune-telling results of the seven days.

密着性試験の評価は、クロスカット試験により全くはが
れないものを○どし、1%未1tのはがれのあるものを
Δ、1%以上のはがれのあるものを×として評画した。
For the evaluation of the adhesion test, those that did not peel off at all in the cross-cut test were evaluated as ○, those that peeled less than 1% as Δ, and those that peeled as much as 1% or more were evaluated as ×.

また、光感度の試験結果も表1に併記した。光感度の測
定は、静電複写紙試験装置(SP−428、川口電機)
を用い、初期表面電位が光減衰により半減するまでの露
光m(半減露光嶽)で比較した0表1の値はそれぞれ2
0個のサングルの平均値を示して−る。
The photosensitivity test results are also listed in Table 1. Photosensitivity was measured using an electrostatic copying paper tester (SP-428, Kawaguchi Electric).
The values in Table 1 were compared using the exposure m until the initial surface potential was halved due to optical attenuation (half-halving exposure).
The average value of 0 samples is shown.

なお上記実施例では、シリコンカップリング剤をグラビ
ア印刷によってつけているが、スクリーン印刷でドツト
状につけても同じ効果が得られる光導電、′−と透明導
電層との″tIiz的接続をよくする為には、シリコン
カップリング材をドツト状又はメツシュ状につけること
が望ましく、全面につけると電気的接続がとれなくなる
In the above example, the silicon coupling agent is applied by gravure printing, but the same effect can be obtained by applying it in dots by screen printing. For this purpose, it is desirable to apply the silicone coupling material in the form of dots or meshes; if it is applied to the entire surface, electrical connection will not be established.

笥1表 〔発明の効果〕 実施例の結果(第1表)から、本発明の電子写真感光体
(第1表の試料1)は、従来の電子写真感光体(第1表
の試料2)に比べ、支持体との審理性が非常に良好であ
り、かつ、光感度の低下もほとんどな1ρという効果を
有する・ 以  上
Table 1 [Effects of the Invention] From the results of the Examples (Table 1), the electrophotographic photoreceptor of the present invention (Sample 1 in Table 1) is superior to the conventional electrophotographic photoreceptor (Sample 2 in Table 1). Compared to the above, it has a very good adhesion with the support and has the effect of 1ρ with almost no decrease in photosensitivity.

Claims (2)

【特許請求の範囲】[Claims] (1)有機光導電性物質、透明導電性物質、および、透
明支持体より成る電子写真感光体において、有機光導電
性物質と透明導電性物質との間にシランカップリング材
の層を形成したことを特徴とする電子写真感光体。
(1) In an electrophotographic photoreceptor consisting of an organic photoconductive substance, a transparent conductive substance, and a transparent support, a layer of a silane coupling material was formed between the organic photoconductive substance and the transparent conductive substance. An electrophotographic photoreceptor characterized by:
(2)前記第1項記載のシランカップリング材がドット
状についていることを特徴とする特許請求の範囲第1項
記載の電子写真感光体。
(2) The electrophotographic photoreceptor according to claim 1, wherein the silane coupling material according to claim 1 is attached in a dot shape.
JP19242086A 1986-08-18 1986-08-18 Electrophotographic sensitive body Pending JPS6348562A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19242086A JPS6348562A (en) 1986-08-18 1986-08-18 Electrophotographic sensitive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19242086A JPS6348562A (en) 1986-08-18 1986-08-18 Electrophotographic sensitive body

Publications (1)

Publication Number Publication Date
JPS6348562A true JPS6348562A (en) 1988-03-01

Family

ID=16291019

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19242086A Pending JPS6348562A (en) 1986-08-18 1986-08-18 Electrophotographic sensitive body

Country Status (1)

Country Link
JP (1) JPS6348562A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5217666A (en) * 1991-05-29 1993-06-08 Daikin Industries Ltd. Process for producing porous polytetrafluoroethylene film
US8011518B2 (en) 2007-09-04 2011-09-06 Fujifilm Corporation Crystalline polymer microporous film, manufacturing method of the same, and filtration filter

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5217666A (en) * 1991-05-29 1993-06-08 Daikin Industries Ltd. Process for producing porous polytetrafluoroethylene film
US8011518B2 (en) 2007-09-04 2011-09-06 Fujifilm Corporation Crystalline polymer microporous film, manufacturing method of the same, and filtration filter

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