JPS5895747A - Film for electrophotography - Google Patents

Film for electrophotography

Info

Publication number
JPS5895747A
JPS5895747A JP19372481A JP19372481A JPS5895747A JP S5895747 A JPS5895747 A JP S5895747A JP 19372481 A JP19372481 A JP 19372481A JP 19372481 A JP19372481 A JP 19372481A JP S5895747 A JPS5895747 A JP S5895747A
Authority
JP
Japan
Prior art keywords
film
receiving layer
toner receiving
resin
substrate
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.)
Granted
Application number
JP19372481A
Other languages
Japanese (ja)
Other versions
JPH0124299B2 (en
Inventor
Teruo Matsunaga
松永 輝雄
Takeo Asai
浅井 武夫
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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP19372481A priority Critical patent/JPS5895747A/en
Publication of JPS5895747A publication Critical patent/JPS5895747A/en
Publication of JPH0124299B2 publication Critical patent/JPH0124299B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G7/00Selection of materials for use in image-receiving members, i.e. for reversal by physical contact; Manufacture thereof
    • G03G7/0006Cover layers for image-receiving members; Strippable coversheets
    • G03G7/002Organic components thereof
    • G03G7/0026Organic components thereof being macromolecular
    • G03G7/004Organic components thereof being macromolecular obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G7/00Selection of materials for use in image-receiving members, i.e. for reversal by physical contact; Manufacture thereof
    • G03G7/0006Cover layers for image-receiving members; Strippable coversheets
    • G03G7/002Organic components thereof
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G7/00Selection of materials for use in image-receiving members, i.e. for reversal by physical contact; Manufacture thereof
    • G03G7/0006Cover layers for image-receiving members; Strippable coversheets
    • G03G7/002Organic components thereof
    • G03G7/0026Organic components thereof being macromolecular
    • G03G7/0046Organic components thereof being macromolecular obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G7/00Selection of materials for use in image-receiving members, i.e. for reversal by physical contact; Manufacture thereof
    • G03G7/006Substrates for image-receiving members; Image-receiving members comprising only one layer
    • G03G7/0073Organic components thereof
    • G03G7/008Organic components thereof being macromolecular

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Laminated Bodies (AREA)

Abstract

PURPOSE:To improve the solvent resistance and the heat resistance of a titled film, by using a oriented polyester film as a substrate and providing a specified toner receiving layer on the substrate. CONSTITUTION:A polymer film having the excellent heat resistance and transparency such as polyethylene terephthalate and polyethylene naphthalate is used as a substrate layer, and a toner receiving layer consisting of spherical plastic powder or a dispersion substance or inorg. fine particles and containing 0.05- 5wt% matting agent having 0.01-10mu average particle diameter and a binder resin insoluble in org. solvent such as a polyester resin, polyether resin and acrylic resin is formed on one side or both surface sides of the substrate layer. The surface specific resistant value of the toner receiving layer is adjusted so as to be in the range of 1X10<9>-1X10<15>OMEGA by incorporating an antistatic agent in the toner receiving layer.

Description

【発明の詳細な説明】 本発明は電子写真用フィルムに関する。更に詳しくは、
ポリエステル配向フィルムを基材とL−1この基材フィ
ルムの少くとも一方の表面に、所定量のマット剤と特定
のバインダーとなる樹脂層を塗設して、表面固有抵抗値
が1×10°からI X 1 G”Ωまでの範囲にある
トナー受領層とした電子写真用フィルムであって、複写
時の搬送性1画健濃度、トナーの密着性に優れ、しかも
耐溶剤性や耐熱性にも優れた電子写真用フィルムに関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electrophotographic film. For more details,
A polyester oriented film is used as a base material and L-1 A predetermined amount of matting agent and a resin layer serving as a specific binder are coated on at least one surface of this base film so that the surface resistivity value is 1 x 10°. An electrophotographic film with a toner-receiving layer in the range from Also relates to excellent electrophotographic films.

従来からプラスチックフィルム、例えばポリエステルフ
ィルム、ポリスルホンフィルム、セルロースエステルフ
ィルム、ホlJカー1’$−)フィルム等が電子写真用
転写機として、使用されている。複写の際のフィルムの
ミスフィードや重送防止、帯電による画惜の乱れの防止
、転写紙へのゴミの付着防止、又は筆記性の改良等のた
め、フィルムは無機化合物のようなマット剤を表面に塗
布されているものが多い。もつとも、従来のマット化フ
ィルムは、マット剤を多量に含んでいるため、不透明で
あるか透明度が低く、電子写真を利用したオーバーヘッ
ドグロジエクション用フィルムや、レントゲン用フィル
ムの如き透明性が要求される用途には利用できなかった
Conventionally, plastic films such as polyester films, polysulfone films, cellulose ester films, HolJCar 1'$-) films, etc. have been used as transfer machines for electrophotography. In order to prevent misfeeds and double feeds of the film during copying, to prevent image distortion due to charging, to prevent dust from adhering to transfer paper, and to improve writing properties, the film is coated with a matting agent such as an inorganic compound. Many are coated on the surface. However, since conventional matte films contain large amounts of matting agents, they are opaque or have low transparency, and require transparency such as films for overhead groggimetry using electrophotography or films for X-rays. It could not be used for any purpose.

そこで、透明性を保持して搬送性(ミスフィード・重送
)、1iji*濃度、トナーとベースフィルムとの層間
の密着性を改良する方法として、有機溶剤可溶のバイン
ダー樹脂と比較的少量のマット剤とからなる組成物であ
って帯電防止処理を施したものをトナー受領層としてベ
ースフィルムの少くとも片方の表面に設ける技術が提案
されている。
Therefore, as a method to maintain transparency and improve conveyance (misfeed/double feed), 1iji* density, and interlayer adhesion between toner and base film, we have developed an organic solvent-soluble binder resin and a relatively small amount of A technique has been proposed in which a composition comprising a matting agent and subjected to antistatic treatment is provided as a toner receiving layer on at least one surface of a base film.

どれと離別に、最近の電子複写機の進歩けめざましく、
非常な高速度複写が実用されつつあり、高速複写の要請
、から、複写時のトナ一定着温度も当然高温度に設定さ
れる傾向にある。
Apart from anything else, recent advances in electronic copying machines have been remarkable.
Extremely high-speed copying is being put into practical use, and due to the demand for high-speed copying, there is a natural tendency for the toner fixation temperature during copying to be set at a high temperature.

ところで、電子写真用フィルムは、オーバーヘッドグロ
ジエクション用フィルムやレントゲン用フィルムなどの
用途にもそのま\転用できるものである。この分野、の
利用に際しては、電子写真用フィルムとしての上述の特
性に加えて、耐溶剤性をも併せ持つ必要が生じてきた。
By the way, electrophotographic films can also be used as they are for overhead glosis films, X-ray films, and the like. When used in this field, it has become necessary to have solvent resistance in addition to the above-mentioned properties as an electrophotographic film.

例えば、複写したフィルムを修正する場合、溶剤を使用
するため、使用するフィルムは耐溶剤性が必要となる。
For example, when a copied film is corrected, a solvent is used, so the film used needs to be resistant to solvents.

すなわち、電子写真用フィルムは、搬送性1画像濃度、
トナーの密着性(接着性)等に優れていると同時に耐溶
剤性、耐熱性を4兼備することが望ましい。
In other words, the electrophotographic film has a transportability of 1 image density,
It is desirable that the toner has excellent adhesion (adhesiveness), etc., as well as solvent resistance and heat resistance.

この観点から、従来提案された方法は、バインダー樹脂
として、溶剤に可溶な樹脂を使用しているため、トナー
受領層を備えたフィルムは耐溶剤、性を有しておらず、
例えば消去液を使用して画像を修正する場合、非常にき
たない画像となってしまう等の欠点を有している。
From this point of view, the conventionally proposed methods use a solvent-soluble resin as the binder resin, so the film provided with the toner receiving layer does not have solvent resistance.
For example, when an erasing liquid is used to correct an image, it has the disadvantage that the image becomes extremely messy.

本発明は、これらの問題点を解消し圧電子写真用フィル
ムを提供するものである。プラスチックフィルムを基材
とし、この基材にトナー受領層を設層するととKより耐
溶剤性及び耐熱性に優れ、複写時にミスフィード重送郷
が起らず、画像濃度が高くベースフィルムとトナーとの
接着性にも優れた電子写真用フィルムを提供するもので
ある。
The present invention solves these problems and provides a piezoelectric photographic film. When a plastic film is used as a base material and a toner receiving layer is formed on this base material, it has better solvent resistance and heat resistance than K, eliminates misfeeds during copying, has high image density, and can easily absorb both base film and toner. The object of the present invention is to provide an electrophotographic film that also has excellent adhesion to.

即ち、本発明は、有機重合体のフィルムを基材層(ベー
スフィルム)とし、該基材層の片方の表面又は両表面に
粒子径が0、O1μ(ミクロン)乃至10/Jのマット
剤0.05重量%乃至5重量%と有機溶媒に不溶性のボ
リヱステル樹宥及び(又は)アクリル樹脂を主成分とす
るバインダー樹脂とを含むトナー受領層を形成せしめて
なり、該トナー受領層の表面固有抵抗値がI X 10
@Ω乃至I X 10’−の範囲である電子写真用フィ
ルムである。
That is, in the present invention, a film of an organic polymer is used as a base material layer (base film), and a matting agent with a particle size of 0, 1μ (micron) to 10/J is provided on one or both surfaces of the base material layer. .05% by weight to 5% by weight and a binder resin mainly composed of polyester resin insoluble in organic solvents and/or acrylic resin, and the surface specific resistance of the toner receiving layer is The value is I x 10
It is an electrophotographic film in the range of @Ω to I x 10'-.

本発明による電子写真用フィルムとしては、ベースフィ
ルムの両表面に樹脂及びマット剤を含有し、且つ表面固
有抵抗値がI X 10’からI X 10”Qの範囲
Ktjるトナー受領層を設けたものが、搬送性に優れか
つ使用時複写面と非複写面の区別をする必要がなく便利
である。もつとも、ベースフィルムの片方の表面にトナ
ー受領層を有するものでもかまわない。但し、この場合
社トナー受領層を設けた反対面に帯電防止層を設けるこ
とが好ましい。
In the electrophotographic film according to the present invention, a toner receiving layer containing a resin and a matting agent and having a surface resistivity in the range of I x 10' to I x 10''Q is provided on both surfaces of the base film. It is convenient because it has excellent transportability and there is no need to distinguish between the copying surface and the non-copying surface during use. However, it is also possible to have a toner receiving layer on one surface of the base film.However, in this case It is preferable to provide an antistatic layer on the opposite side to which the toner receiving layer is provided.

本発明に用い得る有機重合体からなるベースフィルムと
しては、ポリエチレンテレフタレート及びポリス・チ4
Vノナフタレート、郷のポリエステルフィルム、ポリカ
ーダネートフイルム。
Examples of base films made of organic polymers that can be used in the present invention include polyethylene terephthalate and polyethylene terephthalate.
V nonaphthalate, Go's polyester film, polycarbonate film.

セルロースアセテートフィルム、ポリスルフォンフィル
ム、ポリフェニレンオキサイドフィルム、ポリイミドフ
ィルム、ポリアミドフィルム。
Cellulose acetate film, polysulfone film, polyphenylene oxide film, polyimide film, polyamide film.

等の耐熱性及び透明性に優れた重合体フィルムが適当で
ある。殊にポリエチレンテレフタレート及びポリエチレ
ンナフタレート等の熱可塑性の芳香族ポリエステルが好
壕しく使用できる。
Polymer films with excellent heat resistance and transparency, such as, are suitable. In particular, thermoplastic aromatic polyesters such as polyethylene terephthalate and polyethylene naphthalate are preferably used.

そして、ポリエステルフィルムの場合基材としては高度
の寸法安定性を備え、例えば熱収縮率(JISC−23
18)がタテ、ヨコ両方向とも1,5チ以下が好ましく
、1.0チ以下が特に好ましい。
In the case of polyester film, it has a high degree of dimensional stability as a base material, such as heat shrinkage rate (JISC-23
18) is preferably 1.5 inches or less in both the vertical and horizontal directions, and particularly preferably 1.0 inches or less.

前述の如く、複写時の熱定着は180〜200℃の範囲
と比較的高い温度で実施されるため、耐熱性の劣るフィ
ルムでは乾式電子写真複写機で複写するとフィルムの表
面平担性が失われて実用性に乏しい。
As mentioned above, heat fixing during copying is carried out at a relatively high temperature in the range of 180 to 200°C, so if a film with poor heat resistance is copied using a dry electrophotographic copying machine, the surface flatness of the film will be lost. It has little practicality.

本発明に適用できるぺ〒スフィルムは、電子写真用フィ
ルムとしての性能を損わない限り、着色剤、滑剤等の添
加物を含有していてもかまわない。レントゲン用フィル
ムとして使用されるものは、青色に着色されていること
はよく知られているが、この種のフィルムも本発明の基
材に適用できる。
The paste film applicable to the present invention may contain additives such as colorants and lubricants as long as the performance as an electrophotographic film is not impaired. It is well known that films used as X-ray films are colored blue, and this type of film can also be applied to the substrate of the present invention.

本i明に用いられるマット剤として杜、二酸化珪素、炭
酸カルシウム、メルク、クレー等の無機微粒子や、ポリ
エチレン、ポリプロピレン。
The matting agents used in the present invention include inorganic fine particles such as mori, silicon dioxide, calcium carbonate, Merck, clay, etc., polyethylene, and polypropylene.

ポリアクリロニトリル、ポリスチレン、ポリ塩化ビニー
ル、ポリカーボネート、ポリエチレンテレフタレーtな
どの重合体パウダーあるいけ、ディスパージョン体が使
用される。殊に球状のプラスチックパウダーあるいはデ
ィスパージョン体が好ましく使用される。マット剤は平
均微粒子径(1次粒子径)が0.01μからlθμまで
のものが適用でき、トナー受領層の厚みKよ抄マット剤
の粒子径を適宜選択できる。もつとも、マット剤の粒子
径が0.01μ未満であると、フィルムの滑り性が劣り
複写時の給紙トレーからのミスフィード、重送トラブル
が発生しやすくなる。また、lOμを超えると、フィル
ムは粗面となって0.01μ未清の場合と同様フィルム
の滑り性が低下しトラブルが発生しやすくなるほか、複
写画像の鮮明さが損われる。なおマット剤の添加量はバ
インダー樹脂に対して0.01重量%乃至5重量−が適
し、特に好ましくは、0.1重量%から2重量%である
。マット剤の添加量が0,01重量−未満であると、フ
ィルム間の滑り性が低くなり複写時のミスフィードや重
送トラブルが発生しやすい。また、5重量−を超えると
透明性が損われオーバーヘッドプがジエクション用フィ
ルムや、レントゲン用フィルム等には適さない。
Polymer powders, suspensions, and dispersions of polyacrylonitrile, polystyrene, polyvinyl chloride, polycarbonate, polyethylene terephthalate, etc. are used. In particular, spherical plastic powder or dispersion bodies are preferably used. A matting agent having an average fine particle diameter (primary particle diameter) of 0.01 μ to lθμ can be used, and the particle diameter of the paper matting agent can be appropriately selected depending on the thickness K of the toner receiving layer. However, if the particle size of the matting agent is less than 0.01 μm, the slipperiness of the film will be poor and problems such as misfeed from the paper feed tray and double feeding during copying will easily occur. On the other hand, if it exceeds 1Oμ, the surface of the film becomes rough, and the slipperiness of the film decreases, making troubles more likely to occur, as in the case of 0.01μ, and the sharpness of the copied image is impaired. The amount of the matting agent added is suitably 0.01% to 5% by weight, particularly preferably 0.1% to 2% by weight, based on the binder resin. If the amount of the matting agent added is less than 0.01% by weight, the slipperiness between the films will be low and misfeeding or double feeding troubles will easily occur during copying. Further, if the weight exceeds 5 -, transparency is impaired and the film is not suitable for overhead projection films, X-ray films, etc.

本発明に適用できる有機溶剤に不溶なバインダー樹脂成
分としては、ポリス・ステル樹脂、ポリエーテルエステ
ル樹脂、;及びアクリル酸エステル共重合体、メタアク
リル酸エステル共重合体、アクリルスチレン共重合体の
如きアクリル系モノマー成分を30 mol 4以上含
有するアクリル樹脂の少く−ともimが挙げられる。こ
れらのバインダー樹脂は水溶p、乳化性又は水分散性と
して使用できる。また有機溶剤に不溶化された樹脂とし
ては、ポリエステル樹脂、ポリエーテルエステル樹脂又
はアクリル酸エステル樹脂、メタアクリル酸エステル樹
脂、スチレンとアクリル酸エステルの共重合体、スチレ
ンとメタアクリル酸エステルの共重合体、アクリルポリ
オール等の如きアクリル系モノマーを30(2)lチ以
上含有するアクリル樹脂の少くとも1fIIからなる樹
脂を自己架橋または異った重合体間で架橋させることK
より得られるものを含む。更にポリエステル樹脂及び(
または)アクリル樹脂とイソシアネート化合物、アオノ
樹脂、エポキシ樹脂、フェノール性樹脂等とを反応させ
ることによっても不溶化樹脂が得られる。このようなイ
ソシアネート化合物としては1.トリレンジイソシアネ
ー)、P、P’−ジフェニルメタンジイソシアネート、
キシレンジイソシアネート。
Examples of binder resin components insoluble in organic solvents that can be applied to the present invention include polystell resins, polyether ester resins, and acrylic ester copolymers, methacrylic ester copolymers, and acrylic styrene copolymers. Examples of acrylic resins containing 30 mol 4 or more of an acrylic monomer component include at least im. These binder resins can be used as water-soluble, emulsifiable or water-dispersible. Examples of resins insolubilized in organic solvents include polyester resins, polyether ester resins, acrylic ester resins, methacrylic ester resins, copolymers of styrene and acrylic esters, and copolymers of styrene and methacrylic esters. , self-crosslinking or crosslinking between different polymers of an acrylic resin containing 30 (2) l or more of acrylic monomers such as acrylic polyols, etc.
Including those obtained from Furthermore, polyester resin and (
Or) an insolubilized resin can also be obtained by reacting an acrylic resin with an isocyanate compound, an aono resin, an epoxy resin, a phenolic resin, or the like. Examples of such isocyanate compounds include 1. tolylene diisocyanate), P,P'-diphenylmethane diisocyanate,
Xylene diisocyanate.

ヘキサメチレンジイソシアネート′9等が挙げられる。Examples include hexamethylene diisocyanate '9.

エポキシ樹脂としては、ポリヒドロキシ化合物のグリシ
ジルエーテル、ポリカルボン酸のグリシジルエステル等
が適用できる。アミノ樹脂としては、メラミン、グアナ
きン、ベンゾグアナミン、尿素等のアミノ化合物とホル
ムアルデヒドとを反応させて得られるメチロール化アミ
ノ化合物、このメチロール化アミノ化合物をメタノール
、ブタノール等のアルコールでメチル化乃至ブチル化し
九メチロール化アミノ化合物。
As the epoxy resin, glycidyl ethers of polyhydroxy compounds, glycidyl esters of polycarboxylic acids, etc. can be used. Examples of amino resins include methylolated amino compounds obtained by reacting amino compounds such as melamine, guanaquin, benzoguanamine, and urea with formaldehyde, and methylated or butylated methylolated amino compounds with alcohols such as methanol and butanol. Nine-methylolated amino compounds.

或いは、これらの初期縮合物等が適用できる。Alternatively, these initial condensates etc. can be applied.

フェノール樹脂としては、周知のレゾール型フェノール
樹脂等が適用できる。゛この様なポリエステル樹脂及゛
び(または)アクリル樹脂を不溶化したものの中では、
殊に1イソシアネ一ト化合物、メラミン樹脂、エポキシ
樹脂が好ましい。有機溶剤に不溶化された樹脂を4える
ボリエステル、アクリル樹脂、イソシアネート化合物、
エポキシ樹脂もしく社アミノ樹脂等は、有機溶剤に可溶
な形謔で提供されても良く、水溶l 水性エマルジョン
、又はディスパージョンの形で提供されても良い。
As the phenol resin, a well-known resol type phenol resin or the like can be used. Among these insolubilized polyester resins and/or acrylic resins,
Particularly preferred are isocyanate compounds, melamine resins, and epoxy resins. Polyesters, acrylic resins, isocyanate compounds, which contain resins insolubilized in organic solvents,
The epoxy resin, amino resin, etc. may be provided in a form soluble in an organic solvent, or may be provided in the form of an aqueous emulsion or dispersion.

トナー受領層の表面固有抵抗値はI X 10”Ωから
I X 10”Qの範囲が適している。表面固有抵抗値
が1×10−未満の場合は複写時トナー像転写が充分行
われず、転写フィルム上の画e11度が低くなる。これ
に対しI X 10”Ωを超える場合はフィルム取扱い
中に静電気を帯び塵埃が付着しやすく、複写時にミスフ
ィードや重送等のトラブルが発生する れが多い。しか
も表面固有抵抗値がlXl0ゝ1Δを超える場合は複写
時に帯電した電荷が長時間わたって除かれず、フィルム
相互にブロッキングを起こし、取扱いにも支障をきたす
The surface resistivity value of the toner receiving layer is suitably in the range of I x 10''Ω to I x 10''Q. If the surface resistivity value is less than 1.times.10@-, the toner image will not be transferred sufficiently during copying, and the image e11 degrees on the transfer film will be low. On the other hand, if IX exceeds 10"Ω, the film becomes electrostatically charged and dust tends to adhere to it while handling the film, which often causes problems such as misfeeds and double feeds during copying. Moreover, the surface resistivity value is 1X10". If it exceeds 1Δ, the charges accumulated during copying will not be removed for a long time, causing mutual blocking of the films and causing problems in handling.

トナー受領層の表面固有抵抗値をI X 10@からI
 X 10”Ωの範囲に調整するKは公知の方法によれ
ばよいが、有効な手段は帯電防止剤を受骨電防止剤とし
ては、アルキル燐酸エステル塩。
The surface specific resistance value of the toner receiving layer is from I
K may be adjusted to within the range of X 10''Ω by a known method, but an effective method is to use an alkyl phosphate ester salt as the antistatic agent.

アルキル硫酸エステル塩、第4級アンモニウム塩等の公
知のものでよい。
Known salts such as alkyl sulfate salts and quaternary ammonium salts may be used.

トナー受領層は、上記のマット剤及びバインダー樹脂、
要すれば帯電防止剤を含む組成物からなる。更に!子写
真用フィルムの性能を損なわない範囲において熱可塑性
合成樹脂、天然樹脂1着色剤、紫外線吸収剤、安定剤、
滑剤、ブロッキング防止剤、硬化促進剤等を添加するこ
ともできる。
The toner receiving layer contains the above matting agent and binder resin,
It consists of a composition that optionally contains an antistatic agent. Even more! Thermoplastic synthetic resin, natural resin 1 colorant, ultraviolet absorber, stabilizer, within the range that does not impair the performance of the child photographic film.
A lubricant, an antiblocking agent, a curing accelerator, etc. can also be added.

トナー受領層をベースフィルムの少くとも一表面に塗設
することKより本発明の電子写真用フィルムが得られる
The electrophotographic film of the present invention can be obtained by coating at least one surface of the base film with a toner receiving layer.

トナー受領層の塗布は、それ自体周知の塗布機構2例え
ばエアドクターコーター、ブレッドコーター、ロツドコ
ーp−、tイフコーター。
The application of the toner-receiving layer is carried out using application mechanisms 2 which are known per se, such as air doctor coaters, bread coaters, rod coaters, etc.

スクイズトコ−ター1、リバースロールコータ−等を用
いて公知の方法により実施できる。
This can be carried out by a known method using a squeeze coater 1, a reverse roll coater, or the like.

本発明の電子写真用フィルムは、透明性に優れ、かつ耐
溶剤性耐熱性に優れたものであ沙、電子複写機により連
続的に複写を行っても、給紙トレーからのミスフィード
や重送が起らない利点がある。更に静電障害に起因する
画像の乱れや転写不良もなく、得られた画像は鮮明で濃
度が高く、トナー受領層への密着性が優れた転写フィル
ムが得られる。
The electrophotographic film of the present invention has excellent transparency, solvent resistance, and heat resistance, and even when it is continuously copied using an electronic copying machine, it does not suffer from misfeeds or overlapping from the paper feed tray. This has the advantage that no transmission occurs. Furthermore, there is no image disturbance or transfer failure due to electrostatic disturbance, the resulting image is clear and has high density, and a transfer film with excellent adhesion to the toner receiving layer can be obtained.

この電子写真用フィルムは、オーバーヘッドグロジエク
ション用途やレントゲン用途を含む種々の用mK有用で
ある。
This electrophotographic film is useful for a variety of applications, including overhead glosis applications and X-ray applications.

以下に実施例を挙げて、本発明を説明する。The present invention will be explained below with reference to Examples.

実施例中の表面固有抵抗値は、タケダ理研株式会社製の
絶縁計で通電1分後に測定した。測定用サンプルは、温
度23℃、相対湿度65チにおいて24時間調湿したも
のを測定に供した。
The surface resistivity values in Examples were measured 1 minute after energization using an insulation meter manufactured by Takeda Riken Co., Ltd. The sample for measurement was subjected to humidity control for 24 hours at a temperature of 23°C and a relative humidity of 65°C.

軟化点は環球法(JIS−に2531 )により測定し
た。
The softening point was measured by the ring and ball method (JIS-2531).

分子量はvpo法により測定したものである。The molecular weight was measured by the vpo method.

実施例1 スルホン酸ソーダ塩基を含有する水溶性の共重合ポリエ
ステル(分子−315000,軟化点140℃)、水溶
性メチロールメラミン及び架橋触媒を固形分比で67 
:30 :3の割合で配合した10重量−の水溶液1(
10部に、平均粒子径1μの炭酸カルシウムを0.1部
とジオクチルリン酸トリエタノールアミン塩(帯電防止
剤)015部とを添加し、均一に分散せしめた。この水
溶液を厚さ100μのポリエチレンテレフタレート2軸
配向フイルムの両表面に、パーコーターを使用して、塗
布厚みが未乾燥状態で1μになる様に塗布し、130℃
の熱風で3分間加熱処理を施し、透明性が良好で、表面
固有抵抗値がI X 10”Ωの電子写真用フィルムを
得た。このようにして得られた電子写真用フィルムはト
ルエンを含んだガーゼで軽くこすっても、何ら変化が認
められず、耐溶剤性め優れたフィルムで。
Example 1 Water-soluble copolymerized polyester containing sodium sulfonate base (molecule -315000, softening point 140°C), water-soluble methylolmelamine, and crosslinking catalyst at a solid content ratio of 67
:30:3 aqueous solution 1 (10% by weight) (
To 10 parts, 0.1 part of calcium carbonate having an average particle diameter of 1 μm and 015 parts of dioctyl phosphate triethanolamine salt (antistatic agent) were added and uniformly dispersed. This aqueous solution was applied to both surfaces of a polyethylene terephthalate biaxially oriented film with a thickness of 100μ using a percoater so that the coating thickness was 1μ in an undried state, and heated to 130°C.
The film was heat-treated with hot air for 3 minutes to obtain an electrophotographic film with good transparency and a surface resistivity of I x 10''.The electrophotographic film thus obtained did not contain toluene. Even when lightly rubbed with gauze, no change was observed; the film has excellent solvent resistance.

あった。there were.

電子写真用フィルムを高速複写機を使用し、50枚連続
で豪写を行なったところ、亡スフイード及び重送トラブ
ルの発生は皆無であり、得られな複写フィルムはトナー
受領層塗布面及び画像の乱れがなく、かつ画像濃度の高
いものであった。複写によって付着したトナーはトナー
受領層に完全に密着していることは、トナー面にセロ・
・ンテープを耐着した後剥離せしめる接着強度テストを
行ったところ、トナーの脱落が僅か認められた程度であ
った。
When we made 50 continuous copies of electrophotographic film using a high-speed copying machine, there were no problems with dead feed or double feeding, and the resulting copy film had no problems with the toner-receiving layer coating and the image quality. There was no disturbance and the image density was high. The fact that the toner that has adhered to the copying layer is completely adhered to the toner receiving layer means that the toner surface is covered with cello.
・When an adhesive strength test was conducted by peeling off the tape after adhesion, only a slight amount of toner was observed to fall off.

比較例1 メチルエチルケトン/酢酸エチル/トルエン= 1/ 
1/1の混合溶剤に溶解した共重合ポリエステル〔分子
量15000.軟化点165℃〕の10重量%溶液Zo
o部に平均粒子径1μの炭酸カルシウムを0.1部とジ
オクチルリン酸カリウム(帯電防止剤) 0. I 5
部とを添加し、均一に分散せしめた。
Comparative Example 1 Methyl ethyl ketone/ethyl acetate/toluene = 1/
Copolymerized polyester [molecular weight 15,000. 10% by weight solution Zo with a softening point of 165°C]
Part o contains 0.1 part of calcium carbonate with an average particle size of 1 μm and 0.0 part of potassium dioctyl phosphate (antistatic agent). I 5
parts were added and uniformly dispersed.

この溶液を用いて実施例1と同様の方法により表面固有
抵抗値が2 X 10”のフィルムを得た。
Using this solution, a film having a surface resistivity of 2 x 10'' was obtained in the same manner as in Example 1.

このフィルムをトルエンを含んだガーゼで軽く擦ったと
ころ、塗布層(トナー受領層)は簡単に離脱し、耐溶剤
性の乏しい亀のであることが判明した。
When this film was lightly rubbed with gauze containing toluene, the coating layer (toner receiving layer) was easily separated, indicating that the film had poor solvent resistance.

実施例2 スルホン1pNa塩基を含有する水溶性の共重合ポリエ
ステル(分子量s o o o、軟化点140℃)、水
性のアクリル・スチレン共重合体、水溶性のメチロール
メラミン及び架橋触媒を固形分比で55:15:30二
3  の割合で含有する10重量%の水溶液1’OO部
に、平均粒子径L5/jの二酸化珪素0.05部と、ジ
オクチルリン酸カリウム0.10部とを添加してシリカ
をよく分散せしめた。水溶液を用いて、実施例1と同様
の方法により、透明性の良好な表面固有抵抗値が2 X
 10”Ωの電子軍真用フィルムを得た。
Example 2 Water-soluble copolymerized polyester containing sulfone 1pNa base (molecular weight soooo, softening point 140°C), water-based acrylic-styrene copolymer, water-soluble methylolmelamine, and crosslinking catalyst in solid content ratio 0.05 part of silicon dioxide having an average particle size L5/j and 0.10 part of dioctyl potassium phosphate were added to 1'OO part of a 10% by weight aqueous solution containing a ratio of 55:15:3023. The silica was well dispersed. Using an aqueous solution, a surface resistivity value of 2X with good transparency was obtained by the same method as in Example 1.
A film for electronic military use of 10''Ω was obtained.

この電子写真用フィルムはトルエンを含んだガーゼで軽
く擦っても何ら変化が認められず、耐溶剤性の優れたフ
ィルムであった。実施例1と同様の方法によ沙複写テス
トを行ったところ実施例1と同様に複写は良好である結
果が得られた。
This electrophotographic film showed no change even when lightly rubbed with toluene-containing gauze, and was a film with excellent solvent resistance. A sand copy test was conducted in the same manner as in Example 1, and as in Example 1, good copying results were obtained.

実施例3 ヒドロキシル価が30 ayKOH/f  のアクリル
ポリオール及びトリレンジインシアネートを固形分比で
loo:ls  の割合で含有する1011f%の溶液
(メチルエチルケトン/酢酸エチル/トルエン= 1/
 l/1の混合溶剤)100部に平均粒子径3μのポリ
オレフィンのパウダー0,05部と、ジオクチルリン酸
カリウム0.5部とを添加し、ポリオレフィン粉末を均
一に分散せしめた。この溶液番用いて、実施例1と同様
の方法により、透明性の良好な表面固有抵抗値が5×1
61’lΩの電子写真用フィルムを得た。この電子写真
用フィルムはトルエンを含んだガーゼで擦っても、何ら
変化が認められず、耐溶剤性の優れたフィルムであるこ
とが判った。なお!l!施例1と同様の方法により複写
テストも満足すべき結果を得た。
Example 3 A 1011f% solution containing an acrylic polyol with a hydroxyl value of 30 ayKOH/f and tolylene diincyanate in a solid content ratio of loo:ls (methyl ethyl ketone/ethyl acetate/toluene = 1/
0.05 parts of polyolefin powder having an average particle size of 3 μm and 0.5 parts of potassium dioctyl phosphate were added to 100 parts of a 1/1 mixed solvent, and the polyolefin powder was uniformly dispersed. Using this solution number, a surface specific resistance value of 5×1 with good transparency was obtained by the same method as in Example 1.
An electrophotographic film of 61'lΩ was obtained. Even when this electrophotographic film was rubbed with gauze containing toluene, no change was observed, indicating that the film had excellent solvent resistance. In addition! l! A copying test conducted in the same manner as in Example 1 also yielded satisfactory results.

実施例4 スルホン酸N&塩基を含有する水溶性の共重合ポリエス
テル(分子量10000.軟化点170℃)の5%水溶
液100部に平均粒子径5μのポリアクリロニトリルの
パウダー0.015部とジオクチルリン酸モノエタノー
ルアミン塩0.04部とを添加し、ポリアクリロニトリ
ルの粉体を均一に水溶液中に分散せしめた。溶液を、実
施例1と同様の方法により塗布して、透明性の良好な表
面固有抵抗値がI X 10”Ωの電子写真用フィルム
を得た。この電子写真用フィルムはトルエンを含んだガ
ーゼで擦っても何ら変化が認められず、耐溶剤性の優れ
たフィルムであった。
Example 4 0.015 parts of polyacrylonitrile powder with an average particle size of 5 μm and dioctyl phosphate monomer were added to 100 parts of a 5% aqueous solution of a water-soluble copolymerized polyester containing sulfonic acid N and base (molecular weight 10,000, softening point 170°C). 0.04 part of ethanolamine salt was added to uniformly disperse the polyacrylonitrile powder in the aqueous solution. The solution was applied in the same manner as in Example 1 to obtain an electrophotographic film with good transparency and a surface resistivity of I x 10"Ω. This electrophotographic film was coated with toluene-containing gauze. No change was observed even when rubbed with water, and the film had excellent solvent resistance.

実施例1と一様の方法により複写テストを施したところ
、満足すべき結果を得た。
A copying test was carried out in the same manner as in Example 1, and satisfactory results were obtained.

Claims (1)

【特許請求の範囲】[Claims] 重合体フィルムの基材層と該基材層の片方の表面又は両
方の表面にマット剤粒子を含有するバインダー樹脂を塗
設して表itI固有抵抗値をI X 10”Ω乃至t 
x t o”Ωとしたトナー受領層とからなる電子写真
、用フィルムにおいて、バインダー樹脂が有機溶媒に不
溶性のもの又は有機溶媒に不溶化処理されたものである
ポリエステル樹脂及び(又は)アクリル樹脂を主成分と
し、マット剤粒子が0.01μ(ミクロン)乃至10μ
の粒子径をもちo、osJij1%乃至5重量%(対バ
インダー樹脂)分散せしめられてなるトナー受領層が形
成されてなることを特徴とする電子写真用フィルム。
A binder resin containing matting agent particles is coated on the base material layer of the polymer film and one or both surfaces of the base material layer, and the specific resistance value is determined from I x 10"Ω to t.
In an electrophotographic film consisting of a toner receiving layer of As a component, the matting agent particles are 0.01μ (micron) to 10μ
1. An electrophotographic film comprising a toner receiving layer having a particle size of 1% to 5% by weight (relative to the binder resin) dispersed in osJij.
JP19372481A 1981-12-03 1981-12-03 Film for electrophotography Granted JPS5895747A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19372481A JPS5895747A (en) 1981-12-03 1981-12-03 Film for electrophotography

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19372481A JPS5895747A (en) 1981-12-03 1981-12-03 Film for electrophotography

Publications (2)

Publication Number Publication Date
JPS5895747A true JPS5895747A (en) 1983-06-07
JPH0124299B2 JPH0124299B2 (en) 1989-05-11

Family

ID=16312737

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19372481A Granted JPS5895747A (en) 1981-12-03 1981-12-03 Film for electrophotography

Country Status (1)

Country Link
JP (1) JPS5895747A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0332183A2 (en) * 1988-03-11 1989-09-13 E.I. Du Pont De Nemours And Company Electrostatic transparencies containing a polyester support
EP0458481A2 (en) * 1990-05-14 1991-11-27 Imperial Chemical Industries Plc Polymeric film
WO1994015263A1 (en) * 1992-12-18 1994-07-07 Bygraves, Anthony, Eric Printing process
JPH06324509A (en) * 1993-05-14 1994-11-25 Somar Corp Color electrophotographic image receiving sheet
JP2006230488A (en) * 2005-02-22 2006-09-07 Okamura Corp Backrest device of chair, and method for attaching backrest of chair
US7867603B2 (en) * 2004-11-30 2011-01-11 Eastman Kodak Company Coextruded toner receiver layer for electrophotography

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5134734A (en) * 1974-09-19 1976-03-24 Suwa Seikosha Kk
JPS5523150A (en) * 1978-08-09 1980-02-19 Bridgestone Corp Novel polybutadiene rubber composition
JPS5688454A (en) * 1979-12-21 1981-07-17 Toyobo Co Ltd Aqueous dispersion

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5134734A (en) * 1974-09-19 1976-03-24 Suwa Seikosha Kk
JPS5523150A (en) * 1978-08-09 1980-02-19 Bridgestone Corp Novel polybutadiene rubber composition
JPS5688454A (en) * 1979-12-21 1981-07-17 Toyobo Co Ltd Aqueous dispersion

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0332183A2 (en) * 1988-03-11 1989-09-13 E.I. Du Pont De Nemours And Company Electrostatic transparencies containing a polyester support
EP0458481A2 (en) * 1990-05-14 1991-11-27 Imperial Chemical Industries Plc Polymeric film
WO1994015263A1 (en) * 1992-12-18 1994-07-07 Bygraves, Anthony, Eric Printing process
US5842096A (en) * 1992-12-18 1998-11-24 Iso Developments Limited Method of printing monochrome and color images onto a surface
JPH06324509A (en) * 1993-05-14 1994-11-25 Somar Corp Color electrophotographic image receiving sheet
US7867603B2 (en) * 2004-11-30 2011-01-11 Eastman Kodak Company Coextruded toner receiver layer for electrophotography
JP2006230488A (en) * 2005-02-22 2006-09-07 Okamura Corp Backrest device of chair, and method for attaching backrest of chair

Also Published As

Publication number Publication date
JPH0124299B2 (en) 1989-05-11

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