JPS6348562A - Electrophotographic sensitive body - Google Patents
Electrophotographic sensitive bodyInfo
- 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
Links
- 239000000463 material Substances 0.000 claims abstract description 21
- 239000000126 substance Substances 0.000 claims abstract description 14
- 230000008878 coupling Effects 0.000 claims abstract description 7
- 238000010168 coupling process Methods 0.000 claims abstract description 7
- 238000005859 coupling reaction Methods 0.000 claims abstract description 7
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910000077 silane Inorganic materials 0.000 claims abstract description 5
- 108091008695 photoreceptors Proteins 0.000 claims description 11
- 206010034972 Photosensitivity reaction Diseases 0.000 abstract description 9
- 230000036211 photosensitivity Effects 0.000 abstract description 9
- 238000001035 drying Methods 0.000 abstract description 2
- 239000000758 substrate Substances 0.000 abstract 3
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 6
- 239000006087 Silane Coupling Agent Substances 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- 101100258233 Caenorhabditis elegans sun-1 gene Proteins 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 125000005577 anthracene group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 229960005265 selenium sulfide Drugs 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/14—Inert intermediate or cover layers for charge-receiving layers
- G03G5/142—Inert intermediate layers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
Abstract
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、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.
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.
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
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)
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:
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.
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)
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 |
-
1986
- 1986-08-18 JP JP19242086A patent/JPS6348562A/en active Pending
Cited By (2)
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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