JPH0363658A - Electrophotographic sensitive body - Google Patents
Electrophotographic sensitive bodyInfo
- Publication number
- JPH0363658A JPH0363658A JP19805489A JP19805489A JPH0363658A JP H0363658 A JPH0363658 A JP H0363658A JP 19805489 A JP19805489 A JP 19805489A JP 19805489 A JP19805489 A JP 19805489A JP H0363658 A JPH0363658 A JP H0363658A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- coating
- sheet
- surface roughness
- electrophotographic photoreceptor
- 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
- 239000011248 coating agent Substances 0.000 claims abstract description 15
- 238000000576 coating method Methods 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 15
- 239000010419 fine particle Substances 0.000 claims abstract description 14
- 230000003746 surface roughness Effects 0.000 claims abstract description 14
- 239000011230 binding agent Substances 0.000 claims abstract description 13
- 239000002245 particle Substances 0.000 claims abstract description 12
- 108091008695 photoreceptors Proteins 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 12
- -1 polyethylene terephthalate Polymers 0.000 abstract description 10
- 239000011162 core material Substances 0.000 abstract description 9
- 230000006378 damage Effects 0.000 abstract description 8
- 229910052814 silicon oxide Inorganic materials 0.000 abstract description 8
- 238000004804 winding Methods 0.000 abstract description 7
- 229920000515 polycarbonate Polymers 0.000 abstract description 5
- 239000004417 polycarbonate Substances 0.000 abstract description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 4
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 4
- 238000009825 accumulation Methods 0.000 abstract description 2
- 238000001125 extrusion Methods 0.000 abstract description 2
- 239000012530 fluid Substances 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 35
- 239000000049 pigment Substances 0.000 description 7
- 229920005668 polycarbonate resin Polymers 0.000 description 6
- 239000004431 polycarbonate resin Substances 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 229920004011 Macrolon® Polymers 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000006087 Silane Coupling Agent Substances 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 2
- 239000002033 PVDF binder Substances 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 229920003086 cellulose ether Polymers 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
- 229940097275 indigo Drugs 0.000 description 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 2
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- OXYZDRAJMHGSMW-UHFFFAOYSA-N 3-chloropropyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)CCCCl OXYZDRAJMHGSMW-UHFFFAOYSA-N 0.000 description 1
- LVNLBBGBASVLLI-UHFFFAOYSA-N 3-triethoxysilylpropylurea Chemical compound CCO[Si](OCC)(OCC)CCCNC(N)=O LVNLBBGBASVLLI-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 1
- CVQVSVBUMVSJES-UHFFFAOYSA-N dimethoxy-methyl-phenylsilane Chemical compound CO[Si](C)(OC)C1=CC=CC=C1 CVQVSVBUMVSJES-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920003066 styrene-(meth)acrylic acid ester copolymer Polymers 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、シート状又はベルト状電子写真感光体に関す
る。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a sheet-like or belt-like electrophotographic photoreceptor.
従来の技術
シート状又はベルト状電子写真感光体は、ポリエチレン
テレフタレートフィルム等のようなフレキシブルな支持
体の一面に感光層塗膜を設けたものが一般に使用されて
いる。シート状又はベルト状電子写真感光体は、それを
製造する際に、フレキシブルな支持体の上にイクストル
ージョンダイ等を用いて感光層塗膜が成膜され、円筒状
のコア材に巻き取られている。2. Description of the Related Art Sheet-like or belt-like electrophotographic photoreceptors are generally made of a flexible support such as a polyethylene terephthalate film with a photosensitive layer coated on one side. When manufacturing a sheet-like or belt-like electrophotographic photoreceptor, a photosensitive layer coating is formed on a flexible support using an extrusion die, etc., and then wound around a cylindrical core material. It is being
発明が解決しようとする課題
ところで、従来のシート状又はベルト状電子写真感光体
において、支持体の裏面は、表面粗さRz (10点
平均粗さ)が0.1〜未満であり、その様なシート状又
はベルト状電子写真感光体をコア材に巻き取ると、以下
■及び■で述べる現象に起因した力学的な歪みが生じ、
それが塗膜破壊を起こすなどして感光体特性に著しいダ
メージを与えると言う問題があった。■塗膜間の摩擦が
大きいために、巻き取り時の感光体層にかかる張力の均
一化が行われない、■巻き取り後に支持体が収縮による
変形歪みを起こし、これが塗膜の摩擦が大きいために緩
和されない。Problems to be Solved by the Invention By the way, in conventional sheet-like or belt-like electrophotographic photoreceptors, the back surface of the support has a surface roughness Rz (10-point average roughness) of 0.1 to less than 0.1. When a sheet-like or belt-like electrophotographic photoreceptor is wound around a core material, mechanical distortion occurs due to the phenomena described below in ■ and ■.
There is a problem in that this causes significant damage to the characteristics of the photoreceptor, such as causing destruction of the coating film. ■Due to high friction between the coating films, the tension applied to the photoreceptor layer during winding is not equalized.■After winding, the support is deformed due to shrinkage, which causes high friction of the coating film. Not relieved for.
したがって、本発明は、従来の技術における上記のよう
な問題点に鑑みてなされたものである。Therefore, the present invention has been made in view of the above-mentioned problems in the conventional technology.
すなわち、本願発明の目的は、従来のシート状又はベル
ト状電子写真感光体における上記のような欠点を改良し
た電子写真感光体を提供することにある。That is, an object of the present invention is to provide an electrophotographic photoreceptor in which the above-mentioned drawbacks of conventional sheet-like or belt-like electrophotographic photoreceptors are improved.
課題を解決するための手段
本発明の上記目的は、シート状又はベルト状電子写真感
光体における支持体の裏面に微細な凹凸を有するバック
コート層を設け、円筒状コア材に巻き取る際の摩擦係数
を小さくすることによって達成される。Means for Solving the Problems The above-mentioned object of the present invention is to provide a back coat layer having fine irregularities on the back surface of the support in a sheet-like or belt-like electrophotographic photoreceptor, and to reduce friction when winding it around a cylindrical core material. This is achieved by reducing the coefficient.
本発明は、フレキシブルな支持体の表面に感光層塗膜を
有するシート状又はベルト状電子写真感光体において、
該支持体の裏面に、結着樹脂中に微粒子が分散されてな
り、表面粗さRzが0,1〜10mのバックコート層を
設けてなることを特徴とするものである。The present invention provides a sheet-like or belt-like electrophotographic photoreceptor having a photosensitive layer coating on the surface of a flexible support.
It is characterized in that a back coat layer is provided on the back surface of the support, which is made of fine particles dispersed in a binder resin and has a surface roughness Rz of 0.1 to 10 m.
以下、本発明のシート状又はベルト状電子写真感光体に
ついて詳記する。Hereinafter, the sheet-like or belt-like electrophotographic photoreceptor of the present invention will be described in detail.
第1図は、本発明の電子写真感光体の一例の模式的断面
図である。支持体1は導電層Uを有しており、その上に
電荷注入阻止層3及び接着層4を介して、電荷発生層2
(及び電荷輸送層22よりなる感光層2が設けられてい
る。一方、支持体の裏面には、微粒子51が結着樹脂5
2に分散したバックコート層5が形成されている。FIG. 1 is a schematic cross-sectional view of an example of the electrophotographic photoreceptor of the present invention. The support 1 has a conductive layer U, on which a charge generation layer 2 is applied via a charge injection blocking layer 3 and an adhesive layer 4.
(And a photosensitive layer 2 consisting of a charge transport layer 22 is provided.On the other hand, on the back side of the support, fine particles 51 are formed on a binder resin 5.
A back coat layer 5 dispersed in two is formed.
本発明の電子写真感光体における支持体としては、導電
性を付与したフレキシブルなシート又はベルト状のプラ
スチックフィルムが使用される。As the support in the electrophotographic photoreceptor of the present invention, a flexible sheet or belt-shaped plastic film imparted with conductivity is used.
例えば、アルミニウム、ニッケル、クロムなどの金属箔
、アルミニウム、チタニウム、ニッケル、クロム、5U
S1金、バナジウム、スズ、酸化インジゴ顔料等の蒸着
層を設けたポリエチレンテレフタレートフィルム等のプ
ラスチックフィルム或いはシートを使用することができ
る。For example, metal foil such as aluminum, nickel, chromium, aluminum, titanium, nickel, chromium, 5U
A plastic film or sheet such as a polyethylene terephthalate film provided with a deposited layer of S1 gold, vanadium, tin, indigo oxide pigment, etc. can be used.
本発明において、感光層は、可撓性を持たせるために有
機感光材料を用いることが望ましいが、感度の高い無機
光導電性粒子を結着樹脂に分散して、感光層を形成させ
てもよい。又、感光層は第1図に示すように電荷発生層
と電荷輸送層とに分離された機能分離型のものであって
もよい。In the present invention, it is preferable to use an organic photosensitive material for the photosensitive layer in order to provide flexibility, but the photosensitive layer may also be formed by dispersing highly sensitive inorganic photoconductive particles in a binder resin. good. Further, the photosensitive layer may be of a functionally separated type in which the photosensitive layer is separated into a charge generation layer and a charge transport layer as shown in FIG.
その場合において、電荷発生層に用いる電荷発生材料と
しては、アゾ顔料、フタロシアニン顔料、多環牛ノン顔
料、ペリレン顔料、インジゴ顔料、キナクリドン顔料、
酸化亜鉛、三方晶系セレンなと公知のものがあげられる
。In that case, the charge generating materials used in the charge generating layer include azo pigments, phthalocyanine pigments, polycyclic bovine non-pigments, perylene pigments, indigo pigments, quinacridone pigments,
Examples include zinc oxide and trigonal selenium.
又、電荷輸送層に用いられる電荷輸送材料としては、例
えば、アミン系化合物、ヒドラゾン化合物、ピラゾリン
化合物、オキサジアゾール化合物、カルバゾール化合物
など公知のものがあげられる。Furthermore, examples of the charge transport material used in the charge transport layer include known materials such as amine compounds, hydrazone compounds, pyrazoline compounds, oxadiazole compounds, and carbazole compounds.
上記の材料は、それ自体に成膜性がないものが多く、層
形成に際し、結着樹脂が用いられる。結着樹脂としては
、ポリカーボネート、ポリエステル、ポリスチレン、ス
チレン−アクリロニトリル共重合体、ポリメタクリル酸
エステル、スチレン−メタクリル酸エステル共重合体、
ポリビニルブチラール、酢酸ビニル重合体または共重合
体、セルロースエステル又はエーテル、ポリブタジェン
、ポリウレタン、エポキシ樹脂などが用いられる。Many of the above materials do not have film-forming properties themselves, so a binder resin is used when forming the layer. As the binder resin, polycarbonate, polyester, polystyrene, styrene-acrylonitrile copolymer, polymethacrylate ester, styrene-methacrylate ester copolymer,
Polyvinyl butyral, vinyl acetate polymers or copolymers, cellulose esters or ethers, polybutadiene, polyurethane, epoxy resins, etc. are used.
又、ポリビニルカルバゾールなどのように、それ自体が
感光性と成膜性とを有する感光性樹脂を用いる場合は、
他の樹脂を用いることなく単独で使用することが可能で
ある。In addition, when using a photosensitive resin that itself has photosensitivity and film-forming properties, such as polyvinyl carbazole,
It can be used alone without using other resins.
本発明において、感光層と支持体との間には、接着性を
向上するための接着層或いは、電荷注入阻止層を設けて
もよい。In the present invention, an adhesive layer or a charge injection blocking layer may be provided between the photosensitive layer and the support to improve adhesion.
本発明において、上記支持体の裏面に設けられるバック
コート層は、結着樹脂中に微粒子が分散されてなるもの
であり、表面には、微細な凹凸を有する粗面が形成され
ており、その表面粗さRz(10点平均粗さ)が0.1
〜10mの範囲にあることが必要である。なお、本明細
書において、表面粗さRzとは、十点平均粗さであって
、断面曲線から基準長さだけ抜き取った部分において、
平均線に平行、かつ、断面曲線を横切らない直線から縦
倍率の方向に測定した最高から5番目までの山頂の標高
の平均値と、最深から5板目までの谷底までの標高の平
均値との差の値をマイクロメートル(111m)で表わ
したものを意味する。表面粗さが0゜Lmに満たない場
合は、摩擦が大きくなるため、上記した円筒状コア材に
巻き付けられた時に生じる歪み応力を緩和することがで
きず、塗膜の破壊などのダメージを塗膜に与える。また
、IOaを超えると、摩擦力が低下し過ぎるため、コア
材に巻き取る際に巻きずれが発生するなどの不都合が生
じる。In the present invention, the back coat layer provided on the back surface of the support is formed by dispersing fine particles in a binder resin, and has a rough surface with fine irregularities formed on the surface. Surface roughness Rz (10 point average roughness) is 0.1
It is necessary to be within the range of ~10 m. In addition, in this specification, the surface roughness Rz is a ten-point average roughness, and in a portion extracted by a reference length from a cross-sectional curve,
The average value of the elevation of the highest to fifth mountain peaks measured in the direction of vertical magnification from a straight line that is parallel to the average line and does not cross the cross-sectional curve, and the average value of the elevation from the deepest to the fifth valley floor. It means the value of the difference expressed in micrometers (111 m). If the surface roughness is less than 0°Lm, friction will increase, making it impossible to alleviate the strain and stress that occurs when the material is wrapped around the cylindrical core material, which may cause damage such as destruction of the paint film. Give to the membrane. Moreover, if it exceeds IOa, the frictional force decreases too much, resulting in inconveniences such as winding misalignment when winding around the core material.
本発明において、バックコート層表面に微細な凹凸を持
たせるためには、結着樹脂中に微粒子を分散させればよ
いが、微粒子の材質、粒径については、塗膜接着性の低
下を起こさず、裏面からの除電光の透過を妨げない等、
感光体特性を阻害しないものを選択することが必要であ
る。In the present invention, fine particles may be dispersed in the binder resin in order to provide the surface of the back coat layer with fine irregularities, but the material and particle size of the particles must be selected so as not to cause a decrease in coating film adhesion. No, it does not obstruct the transmission of static electricity removal light from the back side, etc.
It is necessary to select a material that does not inhibit the photoreceptor properties.
本発明において使用できる微粒子の材質としては、酸化
ケイ素(S i02 ) 、シランカップリング剤で表
面処理された酸化ケイ素、例えば、メチルトリメトキシ
シラン、フェニルトリメトキシシラン、メチルフエニル
ジメトキシシラン、ジフェニルジメトキシシラン及びそ
の他のアルコキシシラン、ヘキサメチルジシラザンその
他のシラザン、γ−クロロプロピルトリメトキシシラン
、ビニルトリクロロシラン、ビニルトリメトキシシラン
、ビニルトリエトキシシラン、γ−メタクリロキシプロ
ピルトリメトキシシラン、γ−グリシドキシプロビルト
リメトキシシラン、γ−メルカプトプロピルトリメトキ
シシラン、γ−アミノプロピルトリエトキシシラン、γ
−ウレイドプロピルトリエトキシシラン等のシランカッ
プリング剤で処理したものがあげられ、更に酸化カルシ
ウム(CaO)、酸化マグネシウム(MgO)、酸化ア
ルミニウム(A 120i ) 、酸化バリウム(Ba
O)等の金属酸化物、及びポリテトラフルオロエチレン
、ポリクロロトリフルオロエチレン、テトラフルオロエ
チレン−へキサフルオロプロピレン共重合体、ポリフッ
化ビニリデン、ポリフッ化ビニル、エチレン−フルオロ
エチレン共重合体、テトラフルオロエチレン−パーフル
オロアルキルビニルエーテル共重合体等のフッ素樹脂を
あげることができる。Materials for the fine particles that can be used in the present invention include silicon oxide (S i02 ), silicon oxide surface-treated with a silane coupling agent, such as methyltrimethoxysilane, phenyltrimethoxysilane, methylphenyldimethoxysilane, and diphenyldimethoxysilane. Silane and other alkoxysilanes, hexamethyldisilazane and other silazane, γ-chloropropyltrimethoxysilane, vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-glyside Xypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ
- treated with a silane coupling agent such as ureidopropyltriethoxysilane;
metal oxides such as O), and polytetrafluoroethylene, polychlorotrifluoroethylene, tetrafluoroethylene-hexafluoropropylene copolymer, polyvinylidene fluoride, polyvinyl fluoride, ethylene-fluoroethylene copolymer, tetrafluoroethylene Examples include fluororesins such as ethylene-perfluoroalkyl vinyl ether copolymers.
また、これ等微粒子の平均粒径は0.1〜104の範囲
のものが好ましく使用できる。Further, the average particle diameter of these fine particles is preferably in the range of 0.1 to 104.
上記微粒子を分散させる為の結着樹脂としては、ポリカ
ーボネート、ポリエステル、ポリスチレン、スチレン−
アクリロニトリル共重合体、ポリメタクリル酸エステル
、スチレン−メタクリル酸エステル共重合体、ポリビニ
ルブチラール、酢酸ビニル重合体又は共重合体、セルロ
ースエステル又はエーテル、ポリブタジェン、ポリウレ
タン、エポキシ樹脂等が使用できるが、特にポリカーボ
ネートが好ましい。As the binder resin for dispersing the above fine particles, polycarbonate, polyester, polystyrene, styrene-
Acrylonitrile copolymers, polymethacrylic acid esters, styrene-methacrylic acid ester copolymers, polyvinyl butyral, vinyl acetate polymers or copolymers, cellulose esters or ethers, polybutadiene, polyurethane, epoxy resins, etc. can be used, but in particular polycarbonate is preferred.
上記微粒子の配合量は、結着樹脂ポリカーボネートに対
して0.5〜5重量%の範囲で使用するのが好ましい。The blending amount of the fine particles is preferably 0.5 to 5% by weight based on the binder resin polycarbonate.
塗膜は、上記微粒子と結着樹脂を含有する塗布液を周知
の方法で塗布することによって形成することができる。The coating film can be formed by applying a coating liquid containing the above-mentioned fine particles and a binder resin by a well-known method.
塗膜は、膜厚10〜20贋の範囲に形成するのが好まし
い。The coating film is preferably formed to have a thickness in the range of 10 to 20 mm.
実施例 次に、本発明を実施例によって説明する。Example Next, the present invention will be explained by examples.
実施例1
ポリエチレンテレフタレートフィルム表面にチタンを蒸
着してなる厚さ70端の支持体上に、シランカップリン
グ剤よりなる膜厚0.05mの電荷注入阻止層、ポリエ
ステル樹脂(デュポン社製、49000 )よりなる膜
厚0.05tIIAの接着層、三方晶形セレン10部及
びポリ(N−ビニルカルバゾール)50部及びN、N
’−ジフェニルーN、N’−ビス(3−メチルフェニル
)−0,1’−ビフェニル]−4.4’−ジアミン50
部よりなる膜厚3−の電荷発生層、ポリカーボネート樹
脂(モーベイ社製、マクロロン)50部及びN。Example 1 A charge injection blocking layer with a thickness of 0.05 m made of a silane coupling agent and a polyester resin (manufactured by DuPont, 49000) were placed on a support with a thickness of 70 mm formed by vapor-depositing titanium on the surface of a polyethylene terephthalate film. 10 parts of trigonal selenium, 50 parts of poly(N-vinylcarbazole) and N,N
'-diphenyl-N,N'-bis(3-methylphenyl)-0,1'-biphenyl]-4,4'-diamine 50
50 parts of polycarbonate resin (Macrolon, manufactured by Mobay) and N.
N′−ジフェニル−N、N’−ビス(3−メチルフェニ
ル)−0,1’−ビフェニル]−4.4’−ジアミン5
0部よりなる膜厚25mの電荷輸送層を積層した。N'-diphenyl-N,N'-bis(3-methylphenyl)-0,1'-biphenyl]-4,4'-diamine 5
A charge transport layer having a thickness of 25 m and consisting of 0 parts was laminated.
一方、支持体裏面に酸化ケイ素(SiO□)及びポリカ
ーボネート樹脂よりなる膜厚15g、表面粗さRz:L
Oaのバックコート層を形成した。このバックコート層
は、次のようにして形成した。On the other hand, on the back side of the support, a film made of silicon oxide (SiO□) and polycarbonate resin had a thickness of 15 g and a surface roughness Rz: L.
A back coat layer of Oa was formed. This back coat layer was formed as follows.
すなわち、平均粒径10mの酸化ケイ素を、ポリカーボ
ネート樹脂に対して1重量%の量になるように、ポリカ
ーボネート樹脂(モーベイ社製、マクロロン)に添加し
分散させた塗布液を、支持体裏面にイクストルージョン
ダイによって塗布し、100℃の昇温空気で乾燥した。That is, a coating liquid in which silicon oxide with an average particle size of 10 m was added and dispersed in a polycarbonate resin (Macrolon, manufactured by Mobay Co., Ltd.) in an amount of 1% by weight based on the polycarbonate resin was applied onto the back surface of the support. It was applied by a strusion die and dried with heated air at 100°C.
上記のようにして作成された電子写真感光体を、直径2
50 mの円筒状コア材に巻き付けた状態で24時間放
置した後、常法によりコピー操作を行って画像を作成し
、画像評価を行った。その結果、塗膜破壊が原因となる
画質故障は見られなかった。The electrophotographic photoreceptor produced as described above was
After being left wrapped around a 50 m cylindrical core material for 24 hours, a copying operation was performed using a conventional method to create an image, and the image was evaluated. As a result, no image quality failures caused by paint film destruction were observed.
実施例2
実施例1に示した電子写真感光体のバックコート層とし
て、平均粒径0.1〜の酸化ケイ素(Si02)をポリ
カーボネート樹脂(モーベイ社製、マクロロン)に対し
て1重量%分散させてなり、表面粗さ0.1 mの粗面
が形成されたものを有する以外は、実施例1と同様の構
成を有する電子写真感光体を作成し、同様に画像評価を
行った。Example 2 As a back coat layer of the electrophotographic photoreceptor shown in Example 1, 1% by weight of silicon oxide (Si02) having an average particle size of 0.1 to 0.1 was dispersed in a polycarbonate resin (Macrolon, manufactured by Mobay). An electrophotographic photoreceptor having the same structure as in Example 1 was prepared, except that it had a rough surface with a surface roughness of 0.1 m, and image evaluation was performed in the same manner.
その結果、画質欠陥は観察されなかった。As a result, no image quality defects were observed.
実施例3
実施例1に示した電子写真感光体のバックコート層とし
て、平均粒径5aのポリフッ化ビニリデンをポリカーボ
ネート樹脂(モーベイ社製、マクロロン)に対して1重
量%分散させてなり、表面粗さ0.4−の粗面が形成さ
れたものを有する以外は、実施例1と同様の構成を有す
る電子写真感光体を作成し、同様に画像評価を行った。Example 3 The back coat layer of the electrophotographic photoreceptor shown in Example 1 was made by dispersing 1% by weight of polyvinylidene fluoride with an average particle size of 5a in polycarbonate resin (Macrolon, manufactured by Mobay Co., Ltd.) to improve the surface roughness. An electrophotographic photoreceptor having the same structure as in Example 1 was prepared except that a rough surface with a diameter of 0.4- was formed, and image evaluation was performed in the same manner.
その結果、画質欠陥は観察されなかった。As a result, no image quality defects were observed.
比較例1
実施例1に示した電子写真感光体のバックコート層とし
て、酸化ケイ素を分散させないものであって、表面粗さ
0.08IIIaのバックコート層を有する以外は、実
施例1と同様の構成を有する電子写真感光体を作成し、
同様に画像評価を行った。その結果、塗膜破壊に起因す
る画質欠陥が観察された。Comparative Example 1 The same method as in Example 1 was used, except that the back coat layer of the electrophotographic photoreceptor shown in Example 1 did not contain silicon oxide and had a surface roughness of 0.08IIIa. Create an electrophotographic photoreceptor having the following configuration,
Image evaluation was performed in the same manner. As a result, image quality defects due to paint film destruction were observed.
比較例2
実施例1に示した電子写真感光体のバックコート層とて
、平均粒径15−の酸化ケイ素(Si02)微粒子を分
散させ、表面粗さ20sの粗面が形成されたものを有す
る以外は、実施例1と同様の構成を有する電子写真感光
体を作成したところ、lくツクコート層の成膜が均一に
行われず、また、円筒状コア材に巻き取る際に、摩擦が
小さすぎるために巻きずれが起きるなどの不都合が生じ
た。Comparative Example 2 The back coat layer of the electrophotographic photoreceptor shown in Example 1 had a rough surface with a surface roughness of 20s formed by dispersing fine particles of silicon oxide (Si02) with an average particle size of 15. When an electrophotographic photoreceptor having the same configuration as in Example 1 was produced except for this, the film formation of the thin coating layer was not uniform, and the friction was too low when it was wound around a cylindrical core material. This caused inconveniences such as misalignment of the winding.
発明の効果
本発明のシート状又はベルト状電子写真感光体は、上記
のように支持体のバックコート層内に微粒子を分散させ
て所定の表面粗さを有する粗面を形成させたものであり
、それにより円筒状コア材に巻き取る際に、応力歪みの
蓄積がなく、したがって塗膜破壊による感光体特性への
ダメージを防止することが可能である。Effects of the Invention The sheet-like or belt-like electrophotographic photoreceptor of the present invention has fine particles dispersed in the back coat layer of the support to form a rough surface having a predetermined surface roughness, as described above. As a result, there is no accumulation of stress and strain when the material is wound around a cylindrical core material, and therefore, damage to the photoreceptor properties due to paint film breakage can be prevented.
52・・・結着樹脂。52...Binder resin.
Claims (2)
るシート状又はベルト状電子写真感光体において、該支
持体の裏面に、結着樹脂中に微粒子が分散されてなり、
表面粗さRzが0.1〜10μmのバックコート層を設
けてなることを特徴とするシート状又はベルト状電子写
真感光体。(1) In a sheet-like or belt-like electrophotographic photoreceptor having a photosensitive layer coating on the surface of a flexible support, fine particles are dispersed in a binder resin on the back surface of the support,
A sheet-like or belt-like electrophotographic photoreceptor comprising a back coat layer having a surface roughness Rz of 0.1 to 10 μm.
粒子が、平均粒径0.1〜10μmであることを特徴と
する特許請求の範囲第1項に記載のシート状又はベルト
状電子写真感光体。(2) The sheet-like or belt-like electrophotographic photosensitive material according to claim 1, wherein the fine particles in the back coat layer provided on the back surface of the support have an average particle size of 0.1 to 10 μm. body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19805489A JPH0363658A (en) | 1989-08-01 | 1989-08-01 | Electrophotographic sensitive body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19805489A JPH0363658A (en) | 1989-08-01 | 1989-08-01 | Electrophotographic sensitive body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0363658A true JPH0363658A (en) | 1991-03-19 |
Family
ID=16384765
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19805489A Pending JPH0363658A (en) | 1989-08-01 | 1989-08-01 | Electrophotographic sensitive body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0363658A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0759581A1 (en) * | 1995-08-22 | 1997-02-26 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
EP0759580A1 (en) * | 1995-08-22 | 1997-02-26 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
US5753401A (en) * | 1996-01-11 | 1998-05-19 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
US5783351A (en) * | 1996-01-11 | 1998-07-21 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
US7682763B2 (en) * | 2006-07-24 | 2010-03-23 | Xerox Corporation | Imaging member having antistatic anticurl back coating |
KR101699947B1 (en) * | 2016-04-25 | 2017-01-25 | 박범식 | Waterproofing roof structure and system and method for installing the same |
CN110387145A (en) * | 2019-07-18 | 2019-10-29 | 常州大学 | A kind of preparation method of the high abrasion white carbon black for butadiene-styrene rubber reinforcement |
-
1989
- 1989-08-01 JP JP19805489A patent/JPH0363658A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0759581A1 (en) * | 1995-08-22 | 1997-02-26 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
EP0759580A1 (en) * | 1995-08-22 | 1997-02-26 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
EP0759580B1 (en) * | 1995-08-22 | 2000-11-15 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
EP0759581B1 (en) * | 1995-08-22 | 2000-11-15 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
US5753401A (en) * | 1996-01-11 | 1998-05-19 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
US5783351A (en) * | 1996-01-11 | 1998-07-21 | Eastman Kodak Company | Multiactive electrostatographic elements having a support with beads protruding on one surface |
US7682763B2 (en) * | 2006-07-24 | 2010-03-23 | Xerox Corporation | Imaging member having antistatic anticurl back coating |
KR101699947B1 (en) * | 2016-04-25 | 2017-01-25 | 박범식 | Waterproofing roof structure and system and method for installing the same |
CN110387145A (en) * | 2019-07-18 | 2019-10-29 | 常州大学 | A kind of preparation method of the high abrasion white carbon black for butadiene-styrene rubber reinforcement |
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