JPH05281763A - Production of photosensitive body - Google Patents

Production of photosensitive body

Info

Publication number
JPH05281763A
JPH05281763A JP8092592A JP8092592A JPH05281763A JP H05281763 A JPH05281763 A JP H05281763A JP 8092592 A JP8092592 A JP 8092592A JP 8092592 A JP8092592 A JP 8092592A JP H05281763 A JPH05281763 A JP H05281763A
Authority
JP
Japan
Prior art keywords
photosensitive body
thin film
body material
surfactant
base plate
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
JP8092592A
Other languages
Japanese (ja)
Inventor
Kazuo Kobayashi
和夫 小林
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.)
Brother Industries Ltd
Original Assignee
Brother Industries Ltd
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 Brother Industries Ltd filed Critical Brother Industries Ltd
Priority to JP8092592A priority Critical patent/JPH05281763A/en
Publication of JPH05281763A publication Critical patent/JPH05281763A/en
Pending legal-status Critical Current

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  • Photoreceptors In Electrophotography (AREA)

Abstract

PURPOSE:To obtain a uniform photosensitive body material thin film which is restrained pH variation by dispersing a photosensitive body material in an aqueous medium incorporating a pH buffer agent with a surfactant, solubilizing it and forming the photosensitive body material thin film on an electrically conductive base plate. CONSTITUTION:Polyoxyethylene dodecylether, which is a nonionic surfactant, as the surfactant, and lithium bromide as an electrolyte are added to ion- exchanged water so as to be respectively the specified concentrations and besides a boric acid, which is a pH buffer agent, is added, and then the pH is adjusted at the specified value with NaOH. Next beta type copper phthalocyanine, which is a photosensitive body material, is added to the solution and after stirred, ultrasonic wave is applied for a specific hour to prepare a photosensitive body material dispersion solution and it is left standing for 24 hours and supernatant liquid is fractionated to be defined as testing liquid 1. The testing liquid 1 is kept at 60 deg.C in a constant temp. hot water bath 5 and an Al base plate 2 is put in it and a cathode is energized by using a galvanostat 6 to from the photosensitive body thin film on the Al base plate 2.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、電子写真等に用いられ
る感光体の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for manufacturing a photoconductor used in electrophotography and the like.

【0002】[0002]

【従来の技術】従来、感光体の形成方法としては、一般
に、蒸着法、ポリマーバインド法、スリップキャスト法
などが知られている。しかし、蒸着法は感光体材料の種
類によっては分解するおそれがあり、また、ポリマーバ
インド法では、均一な膜を得るのが非常に困難であると
いう問題がある。さらに、スリップキャスト法にあって
は、溶媒等の不純物が入り、その結果、溶媒乾燥時に歪
が生ずると言う問題がある。また、有機溶媒を大量に使
用するため環境上大きな問題となっている。
2. Description of the Related Art Conventionally, vapor deposition, polymer binding, slip casting and the like are generally known as methods for forming a photoconductor. However, the vapor deposition method may decompose depending on the type of the photosensitive material, and the polymer binding method has a problem that it is very difficult to obtain a uniform film. Further, the slip casting method has a problem that impurities such as a solvent enter and as a result, distortion occurs when the solvent is dried. Also, since a large amount of organic solvent is used, it is a serious environmental problem.

【0003】近年、感光体作製時において、感光体材料
である、電荷発生材料、もしくは電荷輸送材料を、水性
溶媒中で界面活性剤によって分散、あるいは可溶化し、
得られる分散液、あるいは溶液中で電解を行って前記材
料からなる電荷発生層、もしくは電荷輸送層を形成する
ことが報告されている。
In recent years, at the time of producing a photoreceptor, a charge generating material or a charge transporting material, which is a photoreceptor material, is dispersed or solubilized in an aqueous solvent with a surfactant,
It has been reported that electrolysis is performed in the resulting dispersion or solution to form a charge generation layer or charge transport layer made of the above-mentioned materials.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、上記方
法で用いられる、分散液、溶液はpH安定性に欠け、連
続使用、長期使用に不向きであり、また、電解処理を行
った場合、電極付近のpHが局部的に変化し、感光体材
料薄膜の生成を妨害すると言う問題点があった。
However, the dispersion and solution used in the above method lack pH stability and are not suitable for continuous use or long-term use. There has been a problem that the pH locally changes and interferes with the formation of a thin film of the photosensitive material.

【0005】本発明は、上述した問題点を解決するため
になされたものであり、pH安定性に優れ、電解処理時
においても、電極付近の局部的なpH変化を抑えること
のできる分散液、溶液を提供することを目的としてい
る。
The present invention has been made to solve the above-mentioned problems, and is a dispersion liquid having excellent pH stability and capable of suppressing a local pH change near the electrode even during electrolytic treatment, It is intended to provide a solution.

【0006】[0006]

【課題を解決するための手段】この目的を達成するため
に本発明の感光体の製造方法は、感光体材料を、pH緩
衝剤を含む水性媒体中で界面活性剤によって分散、ある
いは可溶化する分散可溶化工程と、前記工程により得ら
れた分散液、あるいは溶液を電解液として、導電性基板
を電極として電解を行い、前記感光体材料薄膜を、前記
導電性基板上に形成する感光体材料薄膜形成工程とから
なる。
In order to achieve this object, in the method for producing a photoreceptor of the present invention, the photoreceptor material is dispersed or solubilized by a surfactant in an aqueous medium containing a pH buffer. Dispersion and solubilization step, and a dispersion material or solution obtained in the above step as an electrolytic solution, electrolysis using a conductive substrate as an electrode to form the photosensitive material thin film on the conductive substrate. A thin film forming step.

【0007】[0007]

【作用】上記の構成を有する本発明の感光体の製造方法
によれば、pH緩衝剤の作用により、分散液または溶液
のpH安定性が向上し、連続使用、長期使用が可能とな
り、また、電解による電極付近の局部的なpH変化を抑
え、均一な感光体材料薄膜を形成する。
According to the method for producing a photoreceptor of the present invention having the above-mentioned constitution, the pH stability of the dispersion or solution is improved by the action of the pH buffering agent, which enables continuous use and long-term use. A uniform change in pH near the electrode due to electrolysis is suppressed, and a uniform thin film of a photosensitive material is formed.

【0008】[0008]

【実施例】以下、本発明を具体化した一実施例を図面を
参照して説明する。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the present invention will be described below with reference to the drawings.

【0009】まず、可溶化、分散工程を説明する。界面
活性剤として、非イオン性界面活性剤であるポリオキシ
エチレンドデシルエーテル(Brij35)及び電解質
として臭化リチウム(LiBr)をイオン交換水に、そ
れぞれの濃度が2.0mM(ミリ・モル)及び0.1M(モ
ル)になるように加え、さらにpH緩衝剤であるホウ酸
(H3BO3)を0.1Mになるように加えた後、水酸化
ナトリウム(NaOH)によりpHを9に調製した。
First, the solubilization and dispersion steps will be described. Nonionic surfactant polyoxyethylene dodecyl ether (Brij35) as a surfactant and lithium bromide (LiBr) as an electrolyte in ion-exchanged water at respective concentrations of 2.0 mM (millimolar) and 0. 0.1 M (mol), and then pH buffer boric acid (H 3 BO 3 ) was added to 0.1 M, and the pH was adjusted to 9 with sodium hydroxide (NaOH). ..

【0010】次に、上記溶液に感光体材料であるβ型銅
フタロシアニンを7mMになるように添加し、数時間マ
グネティックスターラーにより攪はんを行った後、30
分間超音波照射を行い感光体材料分散液を作製した。さ
らに、上記分散液を室温にて24時間静置し、上澄み液
を分取して試験液1とした。この試験液のβ型銅フタロ
シアニンの分散濃度を吸光度を用いて測定した結果5m
Mであった、またpHは9でありpH変化は見られなか
った。
Next, β-type copper phthalocyanine, which is a photosensitive material, was added to the above solution so as to have a concentration of 7 mM, and the mixture was stirred with a magnetic stirrer for several hours, and then 30 minutes.
Ultrasonic irradiation was performed for a minute to prepare a photosensitive material dispersion liquid. Further, the above dispersion liquid was allowed to stand at room temperature for 24 hours, and the supernatant was separated to obtain a test liquid 1. As a result of measuring the dispersion concentration of β-type copper phthalocyanine in this test solution using the absorbance, it was 5 m.
It was M, and pH was 9, and no pH change was observed.

【0011】次に、感光体薄膜形成工程を説明する。感
光体薄膜形成工程には、図1に示す3電極セルを用い
た。試料電極(WE)としてアルミニウム基板2を、対極
(CE)として白金板3を、参照電極(RE)としてAg/
AgCl(銀/塩化銀)電極4を用いた。感光体薄膜作
製にあたり、アルミニウム基板2はアセトン中で5分間
超音波脱脂を行った。試験液1を恒温水槽5により60
℃に保ち、その中にアルミニウム基板2を入れ、ガルバ
ノスタット(定電流電源)6を用いて、1分間、−1.
0mA/cm2(ミリ・アンヘ゜ア毎平方センチメートル)でカソード通
電を行うことにより、アルミニウム基板2上に、β型銅
フタロシアニンからなる厚さ約0.2μm(マイクロ・メート
ル)の感光体薄膜を形成した。感光体薄膜形成後の試験
液1のpHは9でありpHの変化は見られなかった。
又、実験後、24時間の後再度感光体薄膜形成実験を行
ったが、同様な結果が得られた。
Next, the photoconductor thin film forming step will be described. The three-electrode cell shown in FIG. 1 was used in the photoconductor thin film forming step. Aluminum substrate 2 as sample electrode (WE), platinum plate 3 as counter electrode (CE), Ag / as reference electrode (RE)
An AgCl (silver / silver chloride) electrode 4 was used. In producing the photoconductor thin film, the aluminum substrate 2 was subjected to ultrasonic degreasing in acetone for 5 minutes. Test solution 1 is put into 60 by constant temperature water tank 5.
C., the aluminum substrate 2 is put therein, and a galvanostat (constant current power supply) 6 is used for 1 minute, -1.
A cathode thin film made of β-type copper phthalocyanine and having a thickness of about 0.2 μm (micrometer) was formed on the aluminum substrate 2 by carrying out cathode energization at 0 mA / cm 2 (millimeter-angle per square centimeter). The pH of the test liquid 1 after forming the photoconductor thin film was 9, and no change in pH was observed.
Further, after 24 hours from the experiment, the photoreceptor thin film forming experiment was conducted again, and similar results were obtained.

【0012】次に、比較のため可溶化、分散工程におい
てpH緩衝剤であるホウ酸を加えず、水酸化ナトリウム
によるpH調製も行わずに、上記実施例と同様の実験を
行った。
Next, for comparison, the same experiment as in the above-mentioned example was carried out without adding boric acid as a pH buffer in the solubilization and dispersion steps and without adjusting the pH with sodium hydroxide.

【0013】その結果pHは、感光体材料分散前はpH
=5.2、分散後はpH=4.6、さらに感光体薄膜形
成後はpH=6.2であり、形成されたβ型銅フタロシ
アニンからなる感光体薄膜の厚みは約0.15μmであ
り、膜は不均一であった。更に、実験後24時間の後、
再度実験を行う前の測定ではpH=4.8であり、再度
形成されたβ型銅フタロシアニンからなる感光体薄膜の
厚みは約0.12μmで、膜も不均一であった。
As a result, the pH is the same as before the dispersion of the photosensitive material.
= 5.2, pH = 4.6 after dispersion, and pH = 6.2 after forming the photoconductor thin film, and the thickness of the photoconductor thin film formed of β-type copper phthalocyanine is about 0.15 μm. , The film was non-uniform. Furthermore, 24 hours after the experiment,
In the measurement before conducting the experiment again, pH was 4.8, and the thickness of the re-formed β-type copper phthalocyanine photoreceptor thin film was about 0.12 μm, and the film was also non-uniform.

【0014】以上より明らかなように、pH緩衝剤を含
む試験液1は、感光体薄膜形成後、放置後においてもp
Hの変化が少なく、再現性良く均一な感光体薄膜を得る
ことができる。これは、pHが一定に保たれるため、電
解時に感光体薄膜形成反応と同時に起こる水の分解によ
る水素発生反応が安定するためと、水素発生により生ず
る電極付近の局部的なpHの上昇が抑えられ、アルミニ
ウム基板2の腐食が抑制されるため、と考えられる。
As is clear from the above, the test liquid 1 containing the pH buffer has a p
It is possible to obtain a uniform photoconductor thin film with little change in H and good reproducibility. This is because the pH is kept constant, and the hydrogen generation reaction due to the decomposition of water that occurs at the same time as the photoconductor thin film formation reaction during electrolysis is stabilized, and the local increase in pH near the electrode caused by hydrogen generation is suppressed It is considered that the corrosion of the aluminum substrate 2 is suppressed.

【0015】[0015]

【発明の効果】以上説明したことから明かなように、本
発明の感光体の製造方法は、pH緩衝剤の作用により、
分散液、もしくは溶液のpHを一定に保つため、電解時
に感光体薄膜形成反応と同時に起こる水の分解反応が安
定するため、連続使用、長期使用が可能となる。また、
水の分解反応により生ずる電極付近の局部的なpHの変
化が抑えられ、基板の腐食が抑制されるため、感光体材
料薄膜が均一になる。
As is apparent from the above description, the method for producing a photoreceptor of the present invention is characterized by the action of the pH buffer agent.
Since the dispersion or the pH of the solution is kept constant, the decomposition reaction of water that occurs at the same time as the reaction of forming a photoreceptor thin film during electrolysis is stable, and continuous use and long-term use are possible. Also,
A local change in pH near the electrode caused by a water decomposition reaction is suppressed, and corrosion of the substrate is suppressed, so that the photosensitive material thin film becomes uniform.

【図面の簡単な説明】[Brief description of drawings]

【図1】実施例において感光体材料薄膜の製造に用いた
3電極セルの構成図である。
FIG. 1 is a configuration diagram of a three-electrode cell used for manufacturing a photosensitive material thin film in Examples.

【符号の説明】[Explanation of symbols]

1 試験液 2 アルミニウム基板 3 白金板 4 Ag/AgCl電極 5 恒温水槽 6 ガルバノスタット 1 Test Solution 2 Aluminum Substrate 3 Platinum Plate 4 Ag / AgCl Electrode 5 Constant Temperature Water Bath 6 Galvanostat

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 電子写真用感光体の製造時において、感
光体材料を、pH(ペーハー:水素イオン濃度)緩衝剤
を含む水性媒体中で界面活性剤によって分散、あるいは
可溶化する分散可溶化工程と、 前記工程により得られた分散液、あるいは溶液を電解液
として、導電性基板を電極として電解を行い、前記感光
体材料薄膜を、前記導電性基板上に形成する感光体材料
薄膜形成工程とからなることを特徴とする感光体の製造
方法。
1. A dispersion solubilization step of dispersing or solubilizing a photoreceptor material in an aqueous medium containing a pH (pH: hydrogen ion concentration) buffer during production of an electrophotographic photoreceptor by a surfactant. And a dispersion liquid obtained in the above step, or a solution as an electrolytic solution, electrolysis is performed using a conductive substrate as an electrode, the photosensitive material thin film, a photosensitive material thin film forming step of forming on the conductive substrate, A method for producing a photoconductor, comprising:
JP8092592A 1992-04-02 1992-04-02 Production of photosensitive body Pending JPH05281763A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8092592A JPH05281763A (en) 1992-04-02 1992-04-02 Production of photosensitive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8092592A JPH05281763A (en) 1992-04-02 1992-04-02 Production of photosensitive body

Publications (1)

Publication Number Publication Date
JPH05281763A true JPH05281763A (en) 1993-10-29

Family

ID=13732013

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8092592A Pending JPH05281763A (en) 1992-04-02 1992-04-02 Production of photosensitive body

Country Status (1)

Country Link
JP (1) JPH05281763A (en)

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