JPH04320268A - Washing method for base of electrophotographic sensitive body - Google Patents
Washing method for base of electrophotographic sensitive bodyInfo
- Publication number
- JPH04320268A JPH04320268A JP11371791A JP11371791A JPH04320268A JP H04320268 A JPH04320268 A JP H04320268A JP 11371791 A JP11371791 A JP 11371791A JP 11371791 A JP11371791 A JP 11371791A JP H04320268 A JPH04320268 A JP H04320268A
- Authority
- JP
- Japan
- Prior art keywords
- base
- water
- washing
- support
- dissolved oxygen
- 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
- 238000005406 washing Methods 0.000 title claims abstract description 7
- 238000000034 method Methods 0.000 title claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 21
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 12
- 239000001301 oxygen Substances 0.000 claims abstract description 12
- 108091008695 photoreceptors Proteins 0.000 claims description 37
- 238000004140 cleaning Methods 0.000 claims description 15
- 238000007254 oxidation reaction Methods 0.000 abstract description 6
- 150000004820 halides Chemical class 0.000 abstract description 4
- 239000002904 solvent Substances 0.000 abstract description 4
- 230000002411 adverse Effects 0.000 abstract description 3
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 239000012535 impurity Substances 0.000 abstract description 3
- -1 hydrocarbon halide Chemical class 0.000 abstract description 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 23
- 239000000126 substance Substances 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 8
- 229910000838 Al alloy Inorganic materials 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 150000008282 halocarbons Chemical class 0.000 description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 229920002799 BoPET Polymers 0.000 description 2
- 239000005041 Mylar™ Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 238000003618 dip coating Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000004334 sorbic acid Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- 239000004419 Panlite Substances 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Photoreceptors In Electrophotography (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は電子写真感光体の製造に
用いる導電性支持体の洗浄方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for cleaning conductive supports used in the production of electrophotographic photoreceptors.
【0002】0002
【従来の技術】一般に電子写真感光体は、導電性支持体
(以下支持体と略す)上に感光層を形成して製造される
。この支持体の材料にはアルミニウム合金が広く用いら
れており、支持体の加工性、寸法安定性、などにおいて
すぐれている。支持体の加工時には、切削油や防錆油な
どの油系物質(灯油、ポリブテン等)が用いられる。
さらに支持体輸送時などに人の指紋等の付着することが
ある。そのため加工後の支持体には必ず油系物質の残査
がありさらには加工時の切削粉、空気中の粉塵等が付着
している。このままの支持体を用いて感光層を形成する
と、均一な層が形成できず感光体としての機能を十分果
さなかったり、感光層が形成できたとしても、この感光
体を用いた電子写真装置(複写機、レーザービームプリ
ンター、LEDプリンター、液晶シャッタープリンター
またはレーザーファクシミリ等)において充分な機能を
発揮できず、特に画像不良を引きおこしてしまう。2. Description of the Related Art Electrophotographic photoreceptors are generally manufactured by forming a photosensitive layer on a conductive support (hereinafter referred to as support). Aluminum alloy is widely used as the material for this support, and is excellent in workability, dimensional stability, etc. of the support. When processing the support, oil-based substances such as cutting oil and antirust oil (kerosene, polybutene, etc.) are used. Furthermore, human fingerprints and the like may adhere to the support during transportation. Therefore, the support after processing always has residues of oil-based substances, and furthermore, there is adhesion of cutting powder during processing, dust in the air, and the like. If a photosensitive layer is formed using the support as it is, a uniform layer may not be formed and the photosensitive member may not function sufficiently, or even if a photosensitive layer is formed, an electrophotographic device using this photoreceptor may not be able to function properly. (copying machines, laser beam printers, LED printers, liquid crystal shutter printers, laser facsimiles, etc.) cannot perform adequately, and particularly causes image defects.
【0003】したがって電子写真感光体を製造する際に
は、支持体を充分に洗浄することが必要である。従来、
電子写真感光体の支持体(主にアルミニウム合金製)を
洗浄するためには、ハロゲン化炭化水素(トリクロロエ
チレン、トリクロロエタン、ジクロロメタンまたは四塩
化炭素等)が、脱脂性、不燃性、速乾性などの面から使
用されてきている。さらには酸やアルカリを用いる方法
も知られている。また、乾式法として、オゾン、紫外線
等を照射し付着物を分解させることにより洗浄する方法
もある。[0003] Therefore, when producing an electrophotographic photoreceptor, it is necessary to thoroughly wash the support. Conventionally,
In order to clean the support of electrophotographic photoreceptors (mainly made of aluminum alloy), halogenated hydrocarbons (trichloroethylene, trichloroethane, dichloromethane, or carbon tetrachloride, etc.) are required to clean the supports (mainly made of aluminum alloy). It has been used since. Furthermore, methods using acids or alkalis are also known. In addition, as a dry method, there is also a method of cleaning by irradiating ozone, ultraviolet rays, etc. to decompose deposits.
【0004】0004
【発明が解決しようとする課題】電子写真技術を用いて
いる分野において、フルカラー複写機、レーザービーム
プリンターなどの開発が盛んに行なわれており、特に高
速化、高画質化、高耐久化が要求されてきている。これ
らの要求に応えるためには、電子写真感光体の支持体の
洗浄度をさらに高めることが必要であることがわかって
きた。現在の支持体洗浄法の主流であるハロゲン化炭化
水素溶剤での洗浄法は、上に述べたような特徴をもつが
、支持体上に微量ではあるがハロゲン化物を残留させて
しまう。従来の電子写真のレベルでは問題にはされなか
ったが、特に高画質化を達成するためには支持体上に残
留したハロゲン化物により、発生する画像欠陥でさえ許
容できない。さらに、ハロゲン化炭化水素溶剤をはじめ
とする有機溶剤は、人体のみならず地域環境に悪影響を
与えてしまう。又、酸やアルカリを用いた場合にも中和
処理の工程や支持体表面の腐食を引き起こしてしまう。
オゾンを用いる方法ではオゾン自体が人体に悪影響であ
り、この方法に限らず、問題点の対策のためには大がか
りの設備が必要であり、その設置場所、費用なども多く
を必要となる。[Problem to be solved by the invention] In the field that uses electrophotography technology, full-color copying machines, laser beam printers, etc. are being actively developed, and there is a particular demand for higher speed, higher image quality, and higher durability. It has been done. In order to meet these demands, it has been found that it is necessary to further improve the cleanliness of the support of the electrophotographic photoreceptor. The cleaning method using a halogenated hydrocarbon solvent, which is the current mainstream method for cleaning a support, has the above-mentioned characteristics, but leaves a trace amount of a halide on the support. Although this has not been a problem at the level of conventional electrophotography, even image defects caused by halides remaining on the support cannot be tolerated, particularly in order to achieve high image quality. Furthermore, organic solvents such as halogenated hydrocarbon solvents have a negative impact not only on the human body but also on the local environment. Furthermore, when acids or alkalis are used, corrosion of the neutralization process and the surface of the support may occur. In the method of using ozone, ozone itself has a negative effect on the human body, and not only this method but also requires large-scale equipment in order to take measures against the problem, and the installation location and cost thereof also require a lot of money.
【0005】そこで、上述の問題点のない水を用いる洗
浄法が注目される。また、不純物の除去を容易にし、か
つ乾燥を容易にする目的で、約40℃以上の温水で処理
することが考えられる。しかし、この方法で支持体に汎
用されるアルミニウム合金を洗浄すると、アルミニウム
合金の表面は活性が高いことや高温という条件より、表
面が酸化反応を起こし、非常に厚い酸化皮膜が形成され
てしまう。この酸化皮膜は、アルミニウム合金の表面特
性を変化させ、またこの変化が感光体全体に一様ではな
いため、感光体を作成する際の部所による塗れ性の違い
や電子写真特性の違いを生じさせてしまう。[0005] Therefore, a cleaning method using water that does not have the above-mentioned problems is attracting attention. Further, in order to facilitate the removal of impurities and facilitate drying, it is conceivable to treat with hot water of about 40° C. or higher. However, when an aluminum alloy commonly used as a support is cleaned using this method, the surface of the aluminum alloy is highly active and the high temperature conditions cause an oxidation reaction on the surface, resulting in the formation of a very thick oxide film. This oxide film changes the surface characteristics of the aluminum alloy, and since this change is not uniform over the entire photoreceptor, it causes differences in paintability and electrophotographic characteristics depending on the part when making the photoreceptor. I'll let you.
【0006】[0006]
【課題を解決するための手段】本発明者は、上述の課題
を解決するために鋭意検討を重ねた結果より、40℃以
上かつ溶存酸素量が1ppm以下の水で洗浄することに
より、感光体支持体をより効果的に洗浄できかつ一様な
塗れ性の支持体が得られ、従って均一な特性をもつ感光
性が作成できることを見い出した。すなわち、本発明は
、電子写真感光体用導電性支持体の洗浄方法において、
少なくとも40℃以上かつ溶存酸素量が1ppm以下の
水で洗浄する工程を有することを特徴とする電子写真感
光体用導電性支持体の洗浄方法である。[Means for Solving the Problems] As a result of extensive studies in order to solve the above-mentioned problems, the present inventors have discovered that a photoreceptor can be cleaned by washing with water at 40° C. or higher and having a dissolved oxygen content of 1 ppm or less. It has been found that the support can be washed more effectively and that a support with uniform coating properties can be obtained, thus making it possible to create photosensitivity with uniform properties. That is, the present invention provides a method for cleaning a conductive support for an electrophotographic photoreceptor, comprising:
A method for cleaning a conductive support for an electrophotographic photoreceptor, comprising a step of cleaning with water at least 40° C. and having a dissolved oxygen amount of 1 ppm or less.
【0007】すなわち、本発明においては、主に水を用
いて洗浄するため、ハロゲン化炭化水素溶剤によるハロ
ゲン化物の残査は発生せず、しかも40℃以上の温水で
処理するため、支持体表面に付着している不純物の除去
が容易である。従来ではこの工程で、高温度であること
と水中の溶存酸素により、感光体支持体のアルミニウム
合金が酸化反応を起こし、支持体表面に酸化皮膜が形成
されていた。しかし、本発明では、酸化反応に関与する
溶存酸素量を1ppm以下としたため、ほとんど酸化反
応が生じず、支持体の表面特性を一様にできるため、均
一な感光体の形成が可能である。That is, in the present invention, since water is mainly used for cleaning, no halide residue is generated due to the halogenated hydrocarbon solvent, and furthermore, since the treatment is performed with hot water of 40° C. or higher, the surface of the support is It is easy to remove impurities attached to the surface. Conventionally, in this process, the aluminum alloy of the photoreceptor support undergoes an oxidation reaction due to the high temperature and dissolved oxygen in the water, resulting in the formation of an oxide film on the surface of the support. However, in the present invention, since the amount of dissolved oxygen involved in the oxidation reaction is set to 1 ppm or less, almost no oxidation reaction occurs and the surface characteristics of the support can be made uniform, making it possible to form a uniform photoreceptor.
【0008】さらに酸化皮膜による電子写真特性への悪
影響がほとんどなくなり、良好な特性を示す。なお本発
明で用いる水は、電導度10μS以下のものがより効果
的である。Furthermore, the adverse effect of the oxide film on the electrophotographic properties is almost eliminated, and good properties are exhibited. Note that water used in the present invention is more effective if its conductivity is 10 μS or less.
【0009】本発明によって洗浄した支持体上に設ける
感光層は無機感光体、有機感光体などに限定されないが
、浸漬塗布法、スプレー塗布法、ブレード塗布法などに
よって塗布される有機感光体の塗布においては特に有効
である。該感光体は、機能分離された電荷発生物質と電
荷輸送物質とが混合された単層型感光体、あるいは電荷
発生物質を含む電荷発生層と、電荷輸送物質を含む電荷
輸送層を積層した積層型感光体などの形態をとる。The photosensitive layer provided on the cleaned support according to the present invention is not limited to inorganic photoreceptors, organic photoreceptors, etc., but organic photoreceptors can be coated by dip coating, spray coating, blade coating, etc. It is particularly effective in The photoreceptor may be a single-layer photoreceptor in which a charge-generating substance and a charge-transporting substance are mixed in a functionally separated manner, or a laminated layer in which a charge-generating layer containing a charge-generating substance and a charge-transporting layer containing a charge-transporting substance are laminated. It takes the form of a type photoreceptor, etc.
【0010】0010
【実施例】以下、本発明を実施例により説明する。
[実施例1]切削加工後のアルミシリンダー(30mm
φ×260mm)を用意した。洗浄剤としてバンライズ
D−20(常磐化学(株))を用い、1wt%水溶液を
調製した。この水溶液に上述のアルミシリンダを浸漬し
、超音波発振器(600W,28kHz)にて1分間処
理した。[Examples] The present invention will be explained below with reference to Examples. [Example 1] Aluminum cylinder (30mm) after cutting
φ×260 mm) was prepared. A 1 wt % aqueous solution was prepared using Vanrise D-20 (Tokiwa Chemical Co., Ltd.) as a cleaning agent. The above-mentioned aluminum cylinder was immersed in this aqueous solution and treated with an ultrasonic oscillator (600 W, 28 kHz) for 1 minute.
【0011】次に脱酸素装置DOR−800(三浦工業
(株))を用いて処理した水(溶存酸素0.5ppm,
温度40℃)が連続的に供給(300リットル/時)さ
れている乾燥槽に上で洗浄したアルミシリンダーを浸漬
し、10秒間停止後次いで引き上げ(1m/min)該
槽上で風乾した。[0011] Next, the water (dissolved oxygen 0.5 ppm,
The aluminum cylinder washed above was immersed in a drying tank to which water (temperature: 40°C) was continuously supplied (300 liters/hour), stopped for 10 seconds, and then pulled up (1 m/min) and air-dried on the tank.
【0012】この洗浄済シリンダーを用いて次に示す電
荷発生層、電荷輸送層を順次積層した電子写真感光体を
作成した。Using this cleaned cylinder, an electrophotographic photoreceptor was prepared in which the following charge generation layer and charge transport layer were sequentially laminated.
【0013】電荷発生物質として構造式[0013] Structural formula as a charge generating substance
【0014】[0014]
【化1】
のジスアゾ顔料10部、ポリビニルブチラール樹脂(エ
スレックBX−1、積水化学製)6部及びシクロヘキサ
ノン50部をガラスビーズを用いたサンドミル装置で分
散した。この分散液にテトラヒドロフラン100部を加
えて、先の洗浄済シリンダー上に塗布して0.2μm厚
の電荷発生層を形成した。10 parts of the disazo pigment of formula 1, 6 parts of polyvinyl butyral resin (S-LEC BX-1, manufactured by Sekisui Chemical Co., Ltd.), and 50 parts of cyclohexanone were dispersed in a sand mill apparatus using glass beads. 100 parts of tetrahydrofuran was added to this dispersion and applied onto the previously cleaned cylinder to form a charge generation layer with a thickness of 0.2 μm.
【0015】次に、構造式Next, the structural formula
【0016】[0016]
【化2】
で表わされるスチルベン化合物10部及びポリカーボネ
ート樹脂(パンライトL−1250、帝人化成製)10
部をジクロロメタン50部及びモノクロロベンゼン10
部に溶解した。10 parts of a stilbene compound represented by [Chemical formula 2] and 10 parts of a polycarbonate resin (Panlite L-1250, manufactured by Teijin Chemicals)
50 parts of dichloromethane and 10 parts of monochlorobenzene
It was dissolved in parts.
【0017】これを上記電荷発生層上に浸漬塗布して1
9μm厚の電荷輸送層を形成した。[0017] This was applied by dip coating on the above charge generation layer.
A charge transport layer having a thickness of 9 μm was formed.
【0018】[実施例2]実施例1において溶存酸素量
を1ppmとした以外は全く同様に感光体を作成した。[Example 2] A photoreceptor was prepared in exactly the same manner as in Example 1 except that the amount of dissolved oxygen was changed to 1 ppm.
【0019】[比較例1]実施例1において脱酸素処理
をしなかった以外は全く同様に感光体を作成した。この
際の溶存酸素量は9ppmであった。[Comparative Example 1] A photoreceptor was prepared in exactly the same manner as in Example 1 except that the deoxidizing treatment was not performed. The amount of dissolved oxygen at this time was 9 ppm.
【0020】[実機試験−1]実施例1,2、比較例1
で作成した感光体についてキヤノン(株)レーザービー
ムプリンター(LBP−SX)で以下の様にして電子写
真特性を評価した。まずマイラーシート(25μm)を
まきつけた標準ドラムが−800Vに帯電するように設
定した。この条件で各感光体の帯電能を測定した。次に
各々の感光体の表面電位を−700Vになるように調整
した後、表面電位を−200Vに下げるために必要な光
量(E200 )を測定した。さらに、強露光後、帯電
なしでの残留電位(Vr)を測定した。その後、これら
の感光体について3000枚の印字を繰り返した後の帯
電能の変化量ΔVd、残留電位の変化量(ΔVr)を測
定した。その結果を表1にまとめた。[Actual Machine Test-1] Examples 1 and 2, Comparative Example 1
The electrophotographic properties of the photoreceptor prepared in the above were evaluated using a laser beam printer (LBP-SX) manufactured by Canon Inc. in the following manner. First, a standard drum wrapped with a Mylar sheet (25 μm) was set to be charged to -800V. The charging ability of each photoreceptor was measured under these conditions. Next, the surface potential of each photoreceptor was adjusted to -700V, and then the amount of light (E200) required to lower the surface potential to -200V was measured. Furthermore, after strong exposure, the residual potential (Vr) without charging was measured. Thereafter, the amount of change in chargeability ΔVd and the amount of change in residual potential (ΔVr) after 3000 sheets of printing were repeated on these photoreceptors were measured. The results are summarized in Table 1.
【0021】[0021]
【表1】
溶存酸素が多い比較例1では実施例1,2と比べて感度
(E200 の必要光量)はほぼ同等であったが帯電能
が著しく低下した。さらに、連続印刷による帯電能の変
化(ΔVd)、残留電位の変化(ΔVr)の絶対値が大
きく、いわゆる電位安定性が低かった。[Table 1] In Comparative Example 1, which contained a large amount of dissolved oxygen, the sensitivity (required light amount for E200) was almost the same as in Examples 1 and 2, but the charging ability was significantly lowered. Furthermore, the absolute values of the change in chargeability (ΔVd) and the change in residual potential (ΔVr) due to continuous printing were large, and the so-called potential stability was low.
【0022】[実施例3]実施例1と全く同様にして得
た洗浄剤シリンダーを用いて次に示す電荷発生層、電荷
輸送層を順次積層した電子写真感光体を作成した。[Example 3] Using a detergent cylinder obtained in exactly the same manner as in Example 1, an electrophotographic photoreceptor was prepared in which the following charge generation layer and charge transport layer were successively laminated.
【0023】電荷発生物質として、構造式As a charge generating substance, structural formula:
【0024】[0024]
【化3】
のジスアゾ顔料10部、ポリビニルブチラール樹脂(エ
スレックBX−1、積水化学製)6部及びシクロヘキサ
ノン50部をガラスビーズを用いたサンドミル装置で分
散した。この分散液にテトラヒドロフラン100部を加
えて、実施例1の方法で洗浄したシリンダー上に塗布し
て0.2μm厚の電荷発生層を形成した。10 parts of the disazo pigment of formula 3, 6 parts of polyvinyl butyral resin (S-LEC BX-1, manufactured by Sekisui Chemical Co., Ltd.), and 50 parts of cyclohexanone were dispersed in a sand mill apparatus using glass beads. 100 parts of tetrahydrofuran was added to this dispersion, and the mixture was coated on the cylinder cleaned by the method of Example 1 to form a charge generation layer with a thickness of 0.2 μm.
【0025】次に実施例1で示した電荷輸送層と同一の
ものを電荷発生層上に塗布して19μm厚の電荷輸送層
を形成し、感光体を作成した。Next, a charge transport layer identical to that shown in Example 1 was coated on the charge generation layer to form a charge transport layer having a thickness of 19 μm, thereby producing a photoreceptor.
【0026】[実施例4]実施例1において水温を50
℃とした以外は全く同様にして洗浄済アルミシリンダー
を得た。このシリンダーに実施例3で示した電荷発生層
と電荷輸送層を順次設け感光体とした。[比較例2]比
較例1で示したのと全く同様の洗浄法、乾燥法を行ない
、実施例3で示した電荷発生層、電荷輸送層を順次設け
感光体とした。[Example 4] In Example 1, the water temperature was set to 50
A cleaned aluminum cylinder was obtained in exactly the same manner except that the temperature was changed to ℃. The charge generation layer and charge transport layer shown in Example 3 were sequentially provided on this cylinder to form a photoreceptor. [Comparative Example 2] The same cleaning and drying methods as those shown in Comparative Example 1 were carried out, and the charge generation layer and charge transport layer shown in Example 3 were sequentially provided to prepare a photoreceptor.
【0027】[実機試験−2]ここで作成した実施例3
,4及び比較例2で作成した感光体をキヤノン製複写機
FC−5に装置した。[Actual machine test-2] Example 3 created here
, 4 and Comparative Example 2 were installed in a Canon copier FC-5.
【0028】まずマイラーシート(25μm)をまきつ
けた標準ドラムが−800Vに帯電するように設定した
。この条件で各感光体の帯電能を測定した。次に各々の
感光体の表面電位を−700Vになるように調整したあ
と表面電位を−200Vに下げるために必要な光量E2
00 を測定した。さらに強露光後、帯電なしでの残留
電位(Vr)を測定した。その後これらの感光体につい
て連続2000枚の印字を繰り返したあとの帯電能の変
化量ΔVd、残留電位の変化量(ΔVr)を測定した。
その結果を表2にまとめた。First, a standard drum wrapped with a Mylar sheet (25 μm) was set to be charged to -800V. The charging ability of each photoreceptor was measured under these conditions. Next, adjust the surface potential of each photoreceptor to -700V, and then calculate the amount of light E2 required to lower the surface potential to -200V.
00 was measured. Furthermore, after strong exposure, the residual potential (Vr) without charging was measured. Thereafter, the amount of change in chargeability ΔVd and the amount of change in residual potential (ΔVr) after 2000 continuous sheets of printing were repeated on these photoreceptors were measured. The results are summarized in Table 2.
【0029】[0029]
【表2】
実施例3、4は高い帯電能が得られているのに対して、
比較例2においては低い値しか得られなかった。また実
施例3,4では、連続複写後も安定した電位特性を示し
た。[Table 2] In Examples 3 and 4, high charging ability was obtained, whereas
In Comparative Example 2, only low values were obtained. Furthermore, Examples 3 and 4 exhibited stable potential characteristics even after continuous copying.
【0030】ここで洗浄し、乾燥の工程を経たアルミシ
リンダーの酸化皮膜の厚さを測定すると、脱酸素した水
により処理したアルミシリンダーでは25Åであるのに
対し、脱酸素していない水で処理したアルミシリンダー
では80Åであった。[0030] When we measure the thickness of the oxide film on the aluminum cylinder that has been washed and dried, it is 25 Å for the aluminum cylinder treated with deoxidized water, whereas it is 25 Å for the aluminum cylinder treated with deoxidized water. In the aluminum cylinder, it was 80 Å.
【0031】[0031]
【発明の効果】このように本発明の電子写真感光体支持
体の洗浄方法によれば、支持体表面の性質を変形させる
ことなく洗浄することができ、支持体からのキャリア注
入などによる電子写真特性の低下を引き起こさない。さ
らに、水系の洗浄方法であるため人体や、地域環境に悪
影響を与えることもない。Effects of the Invention As described above, according to the method for cleaning an electrophotographic photoreceptor support of the present invention, it is possible to clean the support without deforming its surface properties, and it is possible to clean the electrophotographic photoreceptor support by carrier injection from the support. Does not cause deterioration of properties. Furthermore, since it is a water-based cleaning method, it does not have any negative impact on the human body or the local environment.
Claims (2)
方法において、少なくとも40℃以上かつ溶存酸素量が
1ppm以下の水で洗浄する工程を有することを特徴と
する電子写真感光体用導電性支持体の洗浄方法。1. A method for cleaning a conductive support for an electrophotographic photoreceptor, comprising the step of washing with water at least 40° C. and having a dissolved oxygen content of 1 ppm or less. How to clean the support.
下であることを特徴とする請求項1記載の電子写真感光
体用導電性支持体の洗浄方法。2. The method for cleaning a conductive support for an electrophotographic photoreceptor according to claim 1, wherein the conductivity of the cleaning water is 10 μS or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11371791A JPH04320268A (en) | 1991-04-19 | 1991-04-19 | Washing method for base of electrophotographic sensitive body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11371791A JPH04320268A (en) | 1991-04-19 | 1991-04-19 | Washing method for base of electrophotographic sensitive body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04320268A true JPH04320268A (en) | 1992-11-11 |
Family
ID=14619360
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11371791A Pending JPH04320268A (en) | 1991-04-19 | 1991-04-19 | Washing method for base of electrophotographic sensitive body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04320268A (en) |
-
1991
- 1991-04-19 JP JP11371791A patent/JPH04320268A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH0990661A (en) | Electrophotographic photoreceptor | |
JP2007334270A (en) | Method for cleaning substrate for electrophotographic photoreceptor and electrophotographic photoreceptor | |
JPH04320268A (en) | Washing method for base of electrophotographic sensitive body | |
JP3831672B2 (en) | Electrophotographic photosensitive member and electrophotographic apparatus | |
JP2007164008A (en) | Image forming apparatus and image forming method | |
JP3753988B2 (en) | Electrophotographic photosensitive member and electrophotographic apparatus | |
JP2000221719A (en) | Electrophotographic photoreceptor | |
JP6565862B2 (en) | Electrophotographic photosensitive member, process cartridge, and image forming apparatus | |
JPH063831A (en) | Cleaning method for conductive base | |
JP6236809B2 (en) | Electrophotographic photosensitive member and image forming apparatus | |
JP3722176B2 (en) | Method for cleaning electrophotographic photosensitive member substrate, method for producing electrophotographic photosensitive member, and electrophotographic photosensitive member using the same | |
JP3740795B2 (en) | Method for cleaning electrophotographic photoreceptor substrate and method for producing electrophotographic photoreceptor | |
JP3049674B2 (en) | How to wash the support | |
JP3722162B2 (en) | Electrophotographic photoreceptor substrate cleaning method, photoreceptor preparation method, and photoreceptor using the same | |
JP2001188376A (en) | Electrophotographic photoreceptor | |
JPH0611846A (en) | Method for cleaning photo conductive base for electrophotographic sensitive body | |
JP4336677B2 (en) | Electrophotographic photosensitive member and image forming apparatus | |
JP3721703B2 (en) | Method for producing electrophotographic photosensitive member | |
JP5550314B2 (en) | Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus | |
JP3500796B2 (en) | Manufacturing method of electrophotographic photoreceptor | |
JP4726715B2 (en) | Electrophotographic photosensitive member, image forming apparatus, full-color image forming apparatus, and process cartridge | |
JP2000147797A (en) | Electrophotographic photoreceptor for positive electrification | |
JP2002287385A (en) | Electrophotographic sensitive body, its manufacturing method, manufacturing device and image forming device provided with photosensitive body | |
JPH0968821A (en) | Electrophotographic organic photoreceptor | |
JPH06118663A (en) | Production of electrophotographic sensitive body |