JP4389349B2 - Electrophotographic photoreceptor - Google Patents

Description

【００１８】
（一般式（１）中、Ａｒ₁及びＡｒ₂は置換基を有しても良いベンゼン環を表し、Ｘは置換基を有しても良いベンゼン環を表す。Ｒ₁及びＲ₂は、それぞれ水素原子、置換基を有していても良いアルキル基、アリール基のいずれか、またはＲ₁とＲ₂が連結した環状アルキリデン基を表す。）
一般式（１）において、Ｒ₁，Ｒ₂は、水素原子、炭素数３以下のアルキル基、シクロヘキシル基であることは好ましく、水素原子がより好ましい。Ａｒ₁及びＡｒ₂は、メチル基、フェニル基、を有する事、また無置換であることが好ましい。
【００１９】
次に一般式（１）で示される化合物の主な具体例を表−１に示すが、これらに限定されるものではない。これらの構造は、単独では溶解性、液保存安定性に問題がある場合があるので、ジカルボン酸構造部分の異なるものと共重合することが好ましい（共重合の組み合わせの例：Ｐ−１／Ｍ−１，Ｐ−２／Ｍ−２，・・・Ｐ−３６／Ｍ−３６，Ｐ−１／Ｐ−５８，Ｍ−１／Ｐ−５８等）。共重合比は、通常１０／９０〜９０／１０であるが、イソフタル酸を用いる場合には、電気特性の悪化を防ぐために、その比率を５０％以下にすることが好ましく、より好ましくは、３０％以下にすることである。
【００２０】
【表１】

【００２１】
【表２】

【００２２】
【表３】

【００２３】
【表４】

【００２４】
【表５】

【００２５】
【表６】

【００２６】
【表７】

【００２７】
【表８】

【００２８】
【表９】

【００２９】
【表１０】

【００３０】
【表１１】

【００３１】
【表１２】

【００３２】
【表１３】

【００３３】
【表１４】

【００３４】
【表１５】

【００３５】
【表１６】

【００３６】
【表１７】

【００３７】
【表１８】

【００３８】
【表１９】

【００３９】
【表２０】

【００４０】
【表２１】

【００４１】
【表２２】

【００４２】
【表２３】

【００４３】
これらのポリアリレート樹脂中、耐磨耗性、溶剤に対する溶解性の観点から、上記一般式（１）において、Ａｒ₁、Ａｒ₂が下記構造で表され、しかもＲ₁，Ｒ₂がそれぞれ独立に水素原子、あるいはメチル基、あるいは一体となってシクロヘキシル基であるであることが好ましい。
【００４４】
【化５】

【００４５】
（一般式（２）中、Ｒ₃〜Ｒ₆はそれぞれ独立に水素原子、あるいは炭素数５以下の低級アルキル基を表す。）
（３）電荷発生物質
感光層に含有される電荷発生物質としては、セレン及びその合金、ヒ素−セレン、硫化カドミウム、酸化亜鉛、硫化カドミウム、硫化亜鉛、硫化アンチモン、CdS-Se等の合金、酸化チタン等の酸化物系半導体、アモルファスシリコン等のシリコン系材料、その他の無機光導電物質、フタロシアニン、アゾ色素、キナクリドン、多環キノン、ピリリウム塩、ペリレン、インジゴ、チオインジゴ、アントアントロン、ピラントロン、シアニン等の各種有機顔料、色素が使用できる。中でも無金属フタロシアニン、銅、塩化インジウム、塩化ガリウム、シリコン、錫、オキシチタニウム、亜鉛、バナジウム等の金属、又は酸化物、塩化物、水酸化物の配位したフタロシアニン類、モノアゾ、ビスアゾ、トリスアゾ、ポリアゾ類等のアゾ顔料が望ましい。これらのうち、オキシチタニウムフタロシアニンが好ましく、さらに、ＣｕＫα線によるＸ線回折においてブラッグ角（２θ±０．２）２７．３゜に最大回折ピークを示すＹ型結晶がより好ましい。
【００４６】
これらの電荷発生物質は、単独でまたは２種類以上を組み合わせて用いることができる。（４）電荷輸送物質
本発明において、感光層に用いられる電荷輸送物質は、下記一般式（３）で表されるブタジエン系構造を有するものが用いられる。
【００４７】
【化６】

【００４８】
（一般式（３）中、Ｘ₁〜Ｘ₄は置換基を有しても良いフェニル基を表す。）
一般式（３）中、Ｘ₁〜Ｘ₄が有してもよい置換基の例としては、ジメチルアミノ基、ジエチルアミノ基、ジ（１−プロピル）アミノ基、ジ（２ープロピルアミノ）基、ジ（１ーブチル）アミノ基、ジベンジルアミノ基、ジフェニルアミノ基等が挙げられる。好ましい化合物の具体例を表−２に示す。
【００４９】
【表２４】

【００５０】
【表２５】

【００５１】
上記ブタジエン化合物を含有する電荷輸送層は、他の電荷輸送材料を用いた場合よりも、表面抵抗が高い特徴が有り、ＮＯｘガス暴露後、表面抵抗は低下するものの、まだ十分大きいため、画像劣化に至らない。ここで、好ましい表面抵抗値としては、ＮＯｘ等のガス暴露後も、好ましくは２×１０¹³オーム・ｍ以上、より好ましくは５×１０¹³オーム・ｍ以上、さらに好ましくは１×１０¹⁴オーム・ｍ以上を保持していることが望ましい。
【００５２】
なお、本発明においては、上記ブタジエン系電荷輸送材料が主に用いられるが、他の電荷輸送材料と混合して使用することも可能である。この場合、混合には公知のいずれの電荷輸送材料のうち一つあるいは二つ以上を使用することができる。例えば、２，４，７−トリニトロフルオレノンなどの芳香族ニトロ化合物、カルバゾール誘導体、インドール誘導体、イミダゾール誘導体、オキサゾール誘導体、ピラゾール誘導体、オキサジアゾール誘導体、ピラゾリン誘導体、チアジアゾール誘導体などの複素環化合物、アニリン誘導体、ヒドラゾン化合物、芳香族アミン誘導体、スチルベン誘導体、エナミン化合物、これらの化合物が複数結合されたもの、あるいはこれらの化合物からなる基を主鎖もしくは側鎖に有する重合体なが挙げられる。
＜感光層の形成方法＞
上記各層を塗布する際に使用される溶媒、分散媒としては、ブチルアミン、ジエチルアミン、エチレンジアミン、イソプロパノールアミン、トリエタノールアミン、トリエチレンジアミン、Ｎ，Ｎ−ジメチルホルムアミド、アセトン、メチルエチルケトン、シクロヘキサノン、ベンゼン、トルエン、キシレン、クロロホルム、１，２ージクロルエタン、１，２ージクロルプロパン、１，１，２−トリクロルエタン、１，１，１−トリクロルエタン、トリクロルエチレン、テトラクロルエタン、ジクロルメタン、テトラヒドロフラン、ジオキサン、メチルアルコール、エチルアルコール、イソプロピルアルコール、酢酸エチル、酢酸ブチル、ジメチルスルホキシド、メチルセルソルブ、等が挙げられる。
【００５３】
これらの溶媒は、１種単独で使用してもよく、或いは２種以上を混合溶媒として用いても良い。
本発明の電子写真用感光体の感光層は成膜性、可撓性、機械的強度を向上させるために周知の可塑剤を含有していてもよい。
その際、上記塗布液中に添加する可塑剤として、フタル酸エステル、りん酸エステル、エポキシ化合物、塩素化パラフィン、塩素化脂肪酸エステル、メチルナフタレンなどの芳香族化合物などが挙げられる。
【００５４】
感光層の塗布方法としては、スプレー塗布法、スパイラル塗布法、リング塗布法、浸漬塗布法等がある。
スプレー塗布法としては、エアスプレー、エアレススプレー、静電エアスプレー、静電エアレススプレー、回転霧化式静電スプレー、ホットスプレー、ホットエアレススプレー等があるが、均一な膜厚を得るための微粒化度、付着効率等を考えると回転霧化式静電スプレーにおいて、再公表平１−８０５１９８号公報に開示されている搬送方法、すなわち円筒状ワークを回転させながらその軸方向に間隔を開けることなく連続して搬送することにより、総合的に高い付着効率で膜厚の均一性に優れた電子写真感光体を得ることができる。
【００５５】
スパイラル塗布法としては、特開昭５２−１１９６５１号公報に開示されている注液塗布機またはカーテン塗布機を用いた方法、特開平１−２３１９６６号公報に開示されている微小開口部から塗料を筋状に連続して飛翔させる方法、特開平３−１９３１６１号公報に開示されているマルチノズル体を用いた方法等がある。
【００５６】
また浸漬塗布法は、一例としては以下のような手順が挙げられる。
まず、電荷輸送物質（好ましくは前述の化合物）、バインダー、溶剤等を用いて好適な全固形分濃度が２５％以上であってより好ましくは４０％以下の、かつ粘度が通常５０センチポアーズ〜３００センチポアーズ以下、好ましくは１００センチポアーズ〜２００センチポアーズ以下の電荷輸送層形成用の塗布液を調整する。
【００５７】
ここで実質的に塗布液の粘度はバインダーポリマーの種類及びその分子量により決まるが、あまり分子量が低い場合にはポリマー自身の機械的強度が低下するためこれを損わない程度の分子量を持つバインダーポリマーを使用することが好ましい。この様にして調整された塗布液を用いて浸漬塗布法により電荷輸送層が形成される。
【００５８】
その後塗膜を乾燥させ、必要且つ充分な乾燥が行われる様に乾燥温度時間を調整すると良い。乾燥温度は、通常１００〜２５０℃、好ましくは、１１０〜１７０℃、さらに好ましくは、１２０〜１４０℃の範囲である。
乾燥方法としては、熱風乾燥機、蒸気乾燥機、赤外線乾燥機及び遠赤外線乾燥機等を用いることができる。
【００５９】
このようにして形成される感光体にはまた、必要に応じ、下引き層、バリアー層、接着層、ブロッキング層等の中間層、透明絶縁層、あるいは保護層など、電気特性、機械特性の改良のための層を有していてもよいことはいうまでもない。下引き層は通常、感光層と導電性支持体の間に使用され、通常使用される公知のものが使用できる。下引き層としては酸化チタン、酸化アルミニウム、ジルコニア、酸化珪素などの無機微粒子、有機微粒子、ポリアミド樹脂、フェノール樹脂、メラミン樹脂、カゼイン、ポリウレタン樹脂、エポキシ樹脂、セルロース、ニトロセルロース、ポリビニルアルコール、ポリビニルブチラールなどの樹脂等の成分を使用することができる。これらの微粒子、樹脂は単独でまたは２種以上を混合して使用できる。下引き層の厚さは、通常０．０１〜５０μm、好ましくは０．０１〜１０μmである。
【００６０】
感光層と導電性支持体との間に公知のブロッキング層を設けることもできる。本感光体に表面保護層を設ける場合、保護層の厚みは０．０１〜２０μmが可能であり、好ましくは０．１〜１０μmである。
保護層には前記のバインダーを用いることができるが、前記の電荷発生剤、電荷輸送剤、添加剤、金属、金属酸化物、などの導電材料を含有しても良い。ワックスの添加量は０．０１〜３０重量％が可能であり、０．１〜１０重量％が好ましい。
【００６１】
更に、本発明の電子写真用感光体の感光層は成膜性、可とう性、塗布性機械的強度、製膜性、耐久性等を向上させるために周知の可塑剤、酸化防止剤、紫外線吸収剤、レベリング剤を含有していてもよい。
＜積層型感光体＞
・電荷発生層
上述した▲１▼及び▲２▼の積層型感光層を形成する電荷発生層は、前記の電荷発生物質が、バインダー樹脂及び必要に応じ他の有機光導電性化合物、色素、電子吸引性化合物等と共に溶剤に溶解あるいは分散し、こうして得られる塗布液を塗布乾燥して電荷発生層を得る。
【００６２】
電荷発生物質は通常ボールミル、超音波分散器、ペイントシェイカー、アトライター、サンドグラインダ等により適当な分散媒に分散、溶解し、必要に応じてバインダー樹脂を添加して塗布液を調整し、この塗布液をディッピング法、スプレー法、バーコーター法、ブレード法、ロールコーター法、ワイヤーバー塗工法、ナイフコーター塗工法、等の塗布法により塗布後、乾燥する。また電荷発生層は上記電荷発生物質を蒸着、スパッタリング等の気相製膜法で製膜したものであってもよい。
【００６３】
具体的には、電荷発生物質の微粒子を、例えばポリエステル樹脂、ポリビニルアセテート、ポリエステル、ポリカーボネート、ポリビニルアセトアセタール、ポリビニルプロピオナール、ポリビニルブチラール、フェノキシ樹脂、エポキシ樹脂、ウレタン樹脂、セルロースエステル、セルロースエーテルなどの各種バインダー樹脂で結着した形の分散層で使用してもよい。更に、バインダー樹脂としては、スチレン、酢酸ビニル、塩化ビニル、アクリル酸エステル、メタクリル酸エステル、ビニルアルコール、エチルビニルエーテル等のビニル化合物の重合体および共重合体、ポリアミド、けい素樹脂等が挙げられる。この場合の電荷発生材料（電荷発生物質）の使用比率はバインダー樹脂１００重量部に対して通常５〜５００重量部、好ましくは２０〜３００重量部、、電荷発生層の膜厚は通常０．０１〜５μｍ、好ましくは０．０５〜２μｍ、より好ましくは０．１５〜０．８μｍが好適である。また電荷発生層は必要に応じて塗布性を改善するためのレベリング剤や酸化防止剤、増感剤等の各種添加剤を含んでいてもよい。更にまた電荷発生層は上記電荷発生材料の蒸着膜であってもよい。
・電荷輸送層
電荷輸送物質としては、前述したものが使用される。
【００６４】
電荷輸送層に使用されるバインダー樹脂としては、上述した、本発明のポリエステル樹脂の他に、例えばポリメチルメタクリレート、ポリスチレン、ポリ塩化ビニルなどのビニル重合体、及びその共重合体、ポリカーボネート、ポリエステル、ポリエステルカーボネート、ポリスルホン、ポリイミド、フェノキシ、エポキシ、シリコーン樹脂などを共用したり、共重合する事も可能であり、またこれらの部分的架橋硬化物も使用できる。
【００６５】
バインダー樹脂と電荷輸送物質との割合は、バインダー樹脂１００重量部に対して、通常、１０〜２００重量部、好ましくは３０〜１５０重量部の範囲で使用される。
電荷輸送層の膜厚は、通常、１０〜５０μm、好ましくは１３〜３５μmの厚みで使用されるのがよい。
【００６６】
さらに、電荷輸送層には、必要に応じて酸化防止剤、電子吸引性化合物、増感剤等の各種添加剤並びに他の電荷輸送材料を含んでいてもよい。
またこの他に、塗膜の機械的強度や、耐久性向上のための種々の添加剤を用いることができる。この様な添加剤としては、周知の可塑剤や、種々の安定剤、流動性付与剤、架橋剤等が挙げられる。
・感光層の形成方法
電荷発生層と電荷輸送層の二層からなる感光層の場合は、電荷発生層の上に上記塗布液を塗布するか、上記塗布液を塗布して得られる電荷輸送層の上に電荷発生層を形成させることにより、製造することができる。
【００６７】
塗布液調製用の溶剤としてはテトラヒドロフラン、１，４−ジオキサン等のエーテル類、メチルエチルケトン、シクロヘキサノン等のケトン類；トルエン、キシレン等の芳香族炭化水素；Ｎ，Ｎ−ジメチルホルムアミド、アセトニトリル、Ｎ−メチルピロリドン、ジメチルスルホキシド等の非プロトン性極性溶媒；酢酸エチル、蟻酸メチル、メチルセロソルブアセテート等のエステル類；ジクロロエタン、クロロホルム等の塩素化炭化水素などのアミン系化合物を溶解させる溶剤が挙げられる。勿論これらの中からバインダーを溶解するものを選択する必要がある。
【００６８】
このようにして形成される感光体にはまた、必要に応じ、バリアー層、接着層、ブロッキング層等の中間層、透明絶縁層、あるいは保護層など、電気特性、機械特性の改良のための層を有していてもよいことはいうまでもない。
最表面層としては、従来公知の例えば熱可塑性あるいは熱硬化性ポリマーを主体とするオーバーコート層を設けてもよい。
【００６９】
各層の形成方法としては層に含有させる物質を溶剤に溶解または分散させて得られた塗布液を順次塗布する等の公知の方法が適用できる。
＜単層型感光体＞
上述した▲３▼の分散型感光層の場合、用いられる電荷発生物質の種類は、前記したものと同様であるが、その粒子径は充分小さいことが必要であり、好ましくは１μｍ以下、より好ましくは、０．５μｍ以下で使用される。
【００７０】
感光層内に分散される電荷発生物質の量は、例えば０．５〜５０重量％の範囲であるが少なすぎると充分な感度が得られず、多すぎると帯電性の低下、感度の低下などの弊害があり、より好ましくは１〜２０重量％の範囲で使用される。
単層型の感光層は、常法に従って、上述した電荷輸送物質を上述したバインダー樹脂と共に適当な溶剤中に溶解し、必要に応じ、適当な電荷発生材料、増感染料、電子吸引性化合物、他の電荷輸送材料、あるいは、可塑剤、顔料等との周知の添加剤を添加して得られる塗布液を導電性支持体上に塗布、乾燥し、通常、数μ〜数十μ、好ましくは１０〜４５μｍ、特に好ましくは２０μｍ以上の膜厚の層を形成させることにより製造することができる。
＜電子写真感光体＞
このようにして得られる電子写真感光体は長期間にわたって優れた耐刷性を維持する感光体であり、複写機、プリンター、ファックス、製版機等の電子写真分野に好適である。
【００７１】
本発明の電子写真感光体を使用するのにあたって、帯電器はコロトロン、スコロトロンなどのコロナ帯電器、帯電ロール、帯電プラシ等の接触帯電器などが用いられる。露光はハロゲンランプ、蛍光灯、レーザー（半導体、Ｈｅ−Ｎｅ）、ＬＥＤ、感光体内部露光方式等を用いて行われる。現像行程はカスケード現像、１成分絶縁トナー現像、１成分導電トナー現像、二成分磁気ブラシ現像などの乾式現像方式や湿式現像方式などが用いられる。
【００７２】
転写行程はコロナ転写、ローラー転写、ベルト転写などの静電転写法、圧力転写法、粘着転写法が用いられる。定着は熱ローラ定着、フラッシュ定着、オーブン定着、圧力定着などが用いられる。クリーニングにはブラシクリーナー、磁気ブラシクリーナー、静電ブラシクリーナー、磁気ローラークリーナー、ブレードクリーナー、などが用いられる。
【００７３】
【実施例】
以下に本発明を実施例により更に具体的に説明するが、本発明はその要旨を超えない限り、これらの実施例によって限定されるものではない。
なお、実施例中「部」とあるのは、「重量部」を示す。
実施例１
＜感光体の製造＞
ＣｕＫα線によるＸ線回折においてブラッグ角（２θ±０．２）２７．３゜に最大回折ピークを示すＹ型オキシチタニウムフタロシアニン１０重量部を、４−メトキシ−４−メチルペンタノン−２ １５０重量部に加え、サンドグラインドミルにて粉砕分散処理を行った。
【００７４】
また、ポリビニルブチラール（電気化学工業（株）製、商品名デンカブチラール＃６０００Ｃ）の５％ １，２−ジメトキシエタン溶液１００部及びフェノキシ樹脂（ユニオンカーバイド社製、商品名ＰＫＨＨ）の５％ １，２−ジメトキシエタン溶液１００部を混合してバインダー溶液を作製した。
先に作製した顔料分散液１６０重量部に、バインダー溶液１００重量部、適量の１，２−ジメトキシエタンを加え最終的に固形分濃度４．０％の分散液を調製した。
【００７５】
この様にして得られた分散液を表面にアルミ蒸着したポリエチレンテレフタレートフィルム上、あるいは後述する実機試験によるトナーフィルミング評価用にはアルミニウム素管上に、それぞれ膜厚が０．４μｍになるように塗布して電荷発生層を設けた。
次にこのフィルム上に、前記表−２中の電荷輸送性化合物（２）６０部と前記表−１に示したポリエステル(Ｐ−1)と（Ｍ−１）の７０：３０共重合体（粘度平均分子量３５０００）１００重量部をテトラヒドロフラン／トルエン混合溶液５６０重量部で溶解させた溶液をシートの場合はフィルムアプリケータにより塗布し、ドラムの場合は浸せき塗布により塗布し、乾燥後の膜厚が２５μmとなるように電荷輸送層を設けて感光体を作製した。
＜感光体の電気特性の評価＞
次にシート状の電子写真感光体を感光体特性測定[川口電気（株）製モデルＥＰＡ８１００]に装着して、アルミニウム面への流れ込み電流を３５μＡになるように帯電させた後、露光、除電を行い、その時の半減露光量（Ｅ_1/2）、残留電位（Ｖｒ）を測定した。その結果を表−３に示す。
［摩擦試験］
トナーを上記で作成したシート状の感光体の上に０．１ｍｇ／ｃｍ²となるよう均一に乗せ、接触させる面にクリーニングブレードと同じ材質の肉厚２ｍｍのウレタンゴムを１ｃｍ幅に切断したものを４５度の角度で接触させ、荷重２００ｇ、速度５ｍｍ／ｓｅｃ、ストローク２０ｍｍ、繰り返し回数１００回の条件で動摩擦係数を協和界面化学（株）社製全自動摩擦摩耗試験機ＤＦＰＭ−ＳＳで測定した。結果を表−３に示す。
［摩耗試験］
シート状の感光体フィルムを直径１０ｃｍの円状に切断しテーバー摩耗試験機（東洋精機社製）により、摩耗評価を行った。試験条件は、２３℃、５０％ＲＨの雰囲気下、摩耗輪ＣＳ−１０Ｆを用いて、荷重なし（摩耗輪の自重）で１０００回回転後の摩耗量を試験前後の重量を比較することにより測定した。結果を表−３に示す。
［耐ガス性試験］
シート状感光体フィルムを濃度約６ｐｐｍのＮＯｘ雰囲気化に７．５ｈｒ暴露前後の感光体の表面抵抗値を測定した。
【００７６】
実施例２
実施例１において、前記表−２中の電荷輸送性化合物（２）に代えて電荷輸送性化合物（２０）を使用した以外は、実施例１と同様に感光体を作製、評価した。結果を表−３に示す。
比較例１
実施例１において、前記表−２中の電荷輸送性化合物（２）に代えて下記構造の電荷輸送性化合物を使用した以外は、実施例１と同様に感光体を作製、評価した。結果を表−３に示す。
【００７７】
【化７】

【００７８】
比較例２
実施例１において、バインダー樹脂として、ポリエステル樹脂に代えて、下記構造の、粘度平均分子量３１４００のポリカーボネート樹脂を用いた以外は、実施例１と同様に感光体を作製、評価した。結果を表−３に示す。
【００７９】
【化８】

【００８０】
これらの結果から分かるように、本発明の感光体は、電気特性、機械物性に優れるだけでなく、高い表面抵抗を有していることから、ＮＯｘガス暴露後も高い表面抵抗値は高い領域にあり、画像ボケ等の画像劣化を起こしにくく、高画質化の観点から有利であると言える。
【００８１】
【表２６】

【００８２】
【発明の効果】
本発明によれば、長期の繰り返し使用において磨耗が少なく、クリーニング性及びキズに対する耐久性に優れ、さらに、電気特性、塗布性などの他の特性が損なわれない電子写真感光体が提供される。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to an electrophotographic photoreceptor. More particularly, the present invention relates to a highly durable electrophotographic photosensitive member used for a copying machine, a printer, and the like using an electrophotographic process.
[0002]
[Prior art]
In the electrophotographic image forming method by the Carlson method, after the surface of the photoconductor is uniformly charged, the charge is lost by performing exposure according to image information forming the surface, and electrostatic latent image is formed on the surface of the photoconductor. Form an image. Next, the electrostatic latent image is developed and visualized with toner, and further, the toner image is transferred from the photosensitive member to a transfer paper or the like and then fixed. On the other hand, the surface of the photoreceptor after transfer is initialized and repetitively used by removing toner remaining on the surface, removing static electricity, or the like.
[0003]
Therefore, the electrophotographic photosensitive member is required to have photosensitive characteristics such as charging characteristics, good sensitivity, and low dark attenuation, and in repeated use, such as printing durability, abrasion resistance, scratch resistance, and slipperiness. Good mechanical properties, chemical resistance to active species such as ozone and NOx generated during corona discharge, and light resistance to light such as ultraviolet rays are also required.
[0004]
Conventionally, inorganic photoconductive materials such as selenium, selenium-tellurium alloys, arsenic selenide, cadmium sulfide, and zinc oxide have been widely used for electrophotographic photoreceptors. However, these inorganic photoconductive materials are harmful to the human body and have problems such as disposal and increased costs.
For these reasons, photoconductors using an organic photoconductive material for the photosensitive layer, which has a feature of low pollution and easy manufacture, are mainly used. In particular, a laminated type photoconductor composed of a charge generation layer and a charge transfer layer, which separates the function of absorbing light and generating charge from the function of transporting the generated charge, occupies the majority. These photoreceptors are widely used in fields such as copying machines and laser printers.
[0005]
In recent years, electrophotographic copying machines and printers have been required to be able to quickly form a large amount of images and not to be troublesome to maintain. Although printing is indispensable, organic photoreceptors have the disadvantages that they have weaker mechanical properties than inorganic photoreceptors, and are easily worn and damaged when used repeatedly.
[0006]
In order to improve such a defect, various studies have been conducted. Attempts to provide a protective layer on the photosensitive layer have been attempted for some time, but it is difficult to overcome all the problems in terms of manufacturing and durability such as gas resistance such as ozone and NOx. It has not been put into practical use. If the amount of the charge transport material contained in the photosensitive layer is reduced, the amount of wear is reduced, but the photosensitive properties are deteriorated. In addition, when the molecular weight of the binder of the charge transport layer is increased, the amount of wear decreases, but the viscosity of the coating solution increases, so defects such as sagging and unevenness are likely to occur at the coating stage, and the coating speed decreases. However, there is a problem that productivity does not increase. Recently, a method has been devised in which inorganic fillers and lubricating particles are dispersed in the charge transport layer. However, since incident light is scattered by the particles, the sensitivity is greatly deteriorated or the dispersed particles in the coating liquid are left untreated. If there is a defect, such as sedimentation, it is difficult to obtain an electrophotographic photosensitive material having improved mechanical characteristics without impairing the characteristics such as the photosensitive characteristics and coating properties.
[0007]
On the other hand, as one of the major problems with respect to the recent demand for higher image quality, there is an image blur due to deterioration of the surface of the photoreceptor due to an acid gas such as NOx. The main cause of this is thought to be that the charge transport material contained in the photosensitive layer is chemically changed by a gas such as NOx, the surface resistance of the photoreceptor is lowered, and the surface charge is diffused. It is done. Therefore, it is considered necessary that the surface resistance does not fall below a certain level due to such gas exposure as NOx.
[0008]
[Problems to be solved by the invention]
The present invention has been made in view of the above circumstances, and its purpose is to have excellent mechanical properties such as printing durability, abrasion resistance, scratch resistance, slipperiness and the like in repeated use, and acidity such as NOx. An object of the present invention is to provide an electrophotographic photosensitive member that maintains a high surface resistance even after gas exposure, does not cause image blur, and meets the demand for higher image quality.
[0009]
[Means for Solving the Problems]
As a result of intensive studies to solve the above-mentioned problems, the present inventor has found that in an electrophotographic photosensitive member having a photosensitive layer on a conductive support, by adding a specific compound in the outermost layer of the photosensitive layer, charging is performed. The present inventors have found that the above-mentioned mechanical properties are improved without impairing properties, sensitivity, electrical properties such as residual potential, and coating properties.
[0010]
That is, the gist of the present invention is that, in an electrophotographic photoreceptor in which at least a photosensitive layer is formed on a conductive support, the photosensitive layer contains at least a polyester resin and a butadiene-based charge transport material, and the polyester resin is Represented by the general formula (1) (however, the polyester resin is a copolymer in which the dicarboxylic acid structural portion has dicarboxylic acid units derived from isophthalic acid and terephthalic acid, and all of the dicarboxylic acid units derived from isophthalic acid are And 30% or less based on the dicarboxylic acid unit ).
[0011]
DETAILED DESCRIPTION OF THE INVENTION
The present invention is described in detail below.
<Conductive support>
The electrophotographic photosensitive member that is the subject of the present invention has a structure in which at least the photosensitive layer is provided on a conductive support.
[0012]
As the conductive support on which the photosensitive layer is formed, any of those used in known electrophotographic photoreceptors can be used. Specifically, for example, drums, sheets made of metal materials such as aluminum, stainless steel, copper, nickel, zinc, indium, gold, and silver, laminates of these metal foils, deposits, or aluminum, copper, palladium on the surface Insulating supports such as polyester film provided with a conductive layer such as tin oxide, indium oxide, and conductive polymer, paper, and glass. Furthermore, a plastic film, a plastic drum, paper, a paper tube, and the like obtained by applying a conductive material such as metal powder, carbon black, copper iodide, and a polymer electrolyte together with an appropriate binder to conduct a conductive treatment may be used. Further, a plastic sheet or drum containing a conductive material such as metal powder, carbon black, or carbon fiber and becoming conductive can be used. Moreover, a plastic film or a belt subjected to a conductive treatment with a conductive metal oxide such as tin oxide or indium oxide can be used. As described above, the surface of the conductive support can be subjected to various treatments, for example, surface oxidation treatment or chemical treatment within a range that does not affect the image quality.
[0013]
The shape can be any shape such as a drum, a sheet, a belt, and a seamless belt. Among the above, an endless pipe made of metal such as aluminum is a preferable support.
A known barrier layer that is usually used may be provided between the conductive support and the photosensitive layer. Examples of the barrier layer include inorganic layers such as aluminum anodized film, aluminum oxide and aluminum hydroxide, organic layers such as polyvinyl alcohol, casein, polyvinylpyrrolidone, polyacrylic acid, celluloses, gelatin, starch, polyurethane, polyimide and polyamide. Is used.
[0014]
When the organic layer is used as a barrier layer, a metal oxide such as titania, alumina, silica, and zirconium oxide or a metal fine powder such as copper, silver, and aluminum may be dispersed.
The thickness of these barrier layers can be set as appropriate, but is usually in the range of 0.05 to 20 μm, preferably 0.1 to 10 μm.
<Photosensitive layer>
(1) Layer constitution The photosensitive layer is composed of (1) a charge generation layer and a charge transport layer in this order (two-layer type), (2) or a layer in which the charge generation layer and the charge transport layer are reversed (reverse) Any of a so-called dispersion type (single layer type) in which a charge generating substance is dispersed in a charge transport medium can be used.
[0015]
Specifically, the charge generation material is directly deposited or applied as a dispersion with a binder resin to form a charge generation layer, the charge transport material is dissolved together with the polyester, and the dispersion is applied. A layered photoreceptor formed with a charge transport layer (above (1)), a structure in which the order of stacking the charge generation layer and the charge transport layer is reversed (above (2)), or a charge generation material; The charge transport material may be a one-layer type photoconductor (above (3)) coated on a conductive support in a state of being dispersed and dissolved in a binder resin.
(2) Binder resin The electrophotographic photoreceptor of the present invention uses a polyester resin as a binder resin in its photosensitive layer.
[0016]
In the present invention, the polyester used is composed of a polybasic acid component and a polyhydric alcohol component. Examples of the polybasic acid component, anhydrous phthalic acid, terephthalic acid, aromatic saturated acids such as isophthalic acid used et is, as the polyhydric alcohol component, each species bisphenol is used et been under following general formula (1 shown), a wholly aromatic polyester resin (aka: polyarylate resin) has a high glass transition temperature, need for or to exhibit excellent heat resistance, wear resistance et.
[0017]
[Formula 4]

[0018]
(In the general formula (1), Ar ₁ and Ar ₂ represents a benzene ring which may have a substituent group, .R ₁ and R ₂ X is representing the good event benzene ring which may have a substituent Each represents a hydrogen atom, an optionally substituted alkyl group or an aryl group, or a cyclic alkylidene group in which R ₁ and R ₂ are linked.)
In the general formula (1), R ₁ and R ₂ are preferably a hydrogen atom, an alkyl group having 3 or less carbon atoms, or a cyclohexyl group, and more preferably a hydrogen atom. Ar ₁ and Ar ₂ preferably have a methyl group or a phenyl group, and are preferably unsubstituted.
[0019]
Next, major specific examples of the compound represented by the general formula (1) are shown in Table 1, but are not limited thereto. Since these structures alone may have problems in solubility and liquid storage stability, they are preferably copolymerized with different dicarboxylic acid structural parts (examples of copolymerization combinations: P-1 / M). -1, P-2 / M-2, ... P-36 / M-36, P-1 / P-58, M-1 / P-58, etc.). The copolymerization ratio is usually 10/90 to 90/10. However, when isophthalic acid is used, the ratio is preferably 50% or less, more preferably 30%, in order to prevent deterioration of electrical characteristics. % Or less.
[0020]
[Table 1]

[0021]
[Table 2]

[0022]
[Table 3]

[0023]
[Table 4]

[0024]
[Table 5]

[0025]
[Table 6]

[0026]
[Table 7]

[0027]
[Table 8]

[0028]
[Table 9]

[0029]
[Table 10]

[0030]
[Table 11]

[0031]
[Table 12]

[0032]
[Table 13]

[0033]
[Table 14]

[0034]
[Table 15]

[0035]
[Table 16]

[0036]
[Table 17]

[0037]
[Table 18]

[0038]
[Table 19]

[0039]
[Table 20]

[0040]
[Table 21]

[0041]
[Table 22]

[0042]
[Table 23]

[0043]
In these polyarylate resins, from the viewpoint of wear resistance and solubility in solvents, in the above general formula (1), Ar ₁ and Ar ₂ are represented by the following structures, and R ₁ and R ₂ are each independently It is preferably a hydrogen atom, a methyl group, or a cyclohexyl group together.
[0044]
[Chemical formula 5]

[0045]
(In the general formula (2), R _{3 to} R ₆ each independently represents a hydrogen atom or a lower alkyl group having 5 or less carbon atoms.)
(3) Charge generation material The charge generation material contained in the photosensitive layer includes selenium and its alloys, arsenic-selenium, cadmium sulfide, zinc oxide, cadmium sulfide, zinc sulfide, antimony sulfide, alloys such as CdS-Se, oxidation, etc. Oxide-based semiconductors such as titanium, silicon-based materials such as amorphous silicon, other inorganic photoconductive substances, phthalocyanines, azo dyes, quinacridones, polycyclic quinones, pyrylium salts, perylene, indigo, thioindigo, anthrone, pyranthrone, cyanine, etc. Various organic pigments and dyes can be used. Among them, metal-free phthalocyanines, copper, indium chloride, gallium chloride, silicon, tin, oxytitanium, zinc, vanadium, etc., or phthalocyanines coordinated with oxide, chloride, hydroxide, monoazo, bisazo, trisazo, An azo pigment such as polyazo is desirable. Of these, oxytitanium phthalocyanine is preferable, and a Y-type crystal that exhibits a maximum diffraction peak at a Bragg angle (2θ ± 0.2) of 27.3 ° in X-ray diffraction by CuKα rays is more preferable.
[0046]
These charge generation materials can be used alone or in combination of two or more. (4) in the charge-transporting substance present invention, a charge-transporting material used in the photosensitive layer is needed use those having a butadiene structure represented by the following general formula (3).
[0047]
[Chemical 6]

[0048]
(In the general formula (3), X ₁ ~X ₄ represents a phenyl group which may have a substituent.)
In the general formula ( 3 ), examples of the substituent that X _{1 to} X ₄ may have include a dimethylamino group, a diethylamino group, a di (1-propyl) amino group, a di (2-propylamino) group, a di ( 1-butyl) amino group, dibenzylamino group, diphenylamino group and the like. Specific examples of preferred compounds are shown in Table 2.
[0049]
[Table 24]

[0050]
[Table 25]

[0051]
The charge transport layer containing the above butadiene compound has a characteristic that the surface resistance is higher than when other charge transport materials are used, and although the surface resistance decreases after exposure to NOx gas, it is still sufficiently large. Not reached. Here, the preferable surface resistance value is preferably 2 × 10 ¹³ ohm · m or more, more preferably 5 × 10 ¹³ ohm · m or more, even more preferably 1 × 10 ¹⁴ ohm · m, even after exposure to gas such as NOx. It is desirable to hold m or more.
[0052]
In the present invention, the butadiene-based charge transport material is mainly used, but it can also be used by mixing with other charge transport materials. In this case, one or more of any known charge transport materials can be used for mixing. For example, aromatic nitro compounds such as 2,4,7-trinitrofluorenone, carbazole derivatives, indole derivatives, imidazole derivatives, oxazole derivatives, pyrazole derivatives, oxadiazole derivatives, pyrazoline derivatives, heterocyclic compounds such as thiadiazole derivatives, anilines Derivatives, hydrazone compounds, aromatic amine derivatives, stilbene derivatives, enamine compounds, those in which a plurality of these compounds are bonded, or polymers having groups composed of these compounds in the main chain or side chain.
<Method for forming photosensitive layer>
Solvents and dispersion media used when applying the above layers include butylamine, diethylamine, ethylenediamine, isopropanolamine, triethanolamine, triethylenediamine, N, N-dimethylformamide, acetone, methyl ethyl ketone, cyclohexanone, benzene, toluene, Xylene, chloroform, 1,2-dichloroethane, 1,2-dichloropropane, 1,1,2-trichloroethane, 1,1,1-trichloroethane, trichloroethylene, tetrachloroethane, dichloromethane, tetrahydrofuran, dioxane, methyl alcohol , Ethyl alcohol, isopropyl alcohol, ethyl acetate, butyl acetate, dimethyl sulfoxide, methyl cellosolve, and the like.
[0053]
These solvents may be used alone or in combination of two or more.
The photosensitive layer of the electrophotographic photoreceptor of the present invention may contain a known plasticizer in order to improve the film forming property, flexibility, and mechanical strength.
At that time, examples of the plasticizer added to the coating solution include aromatic compounds such as phthalic acid esters, phosphoric acid esters, epoxy compounds, chlorinated paraffins, chlorinated fatty acid esters, and methylnaphthalene.
[0054]
Examples of the photosensitive layer coating method include a spray coating method, a spiral coating method, a ring coating method, and a dip coating method.
Spray coating methods include air spray, airless spray, electrostatic air spray, electrostatic airless spray, rotary atomizing electrostatic spray, hot spray, and hot airless spray. Considering the degree of conversion, adhesion efficiency, etc., in the rotary atomizing electrostatic spray, the conveying method disclosed in the republished Japanese Patent Publication No. 1-805198, that is, the cylindrical workpiece is rotated while the axial direction is spaced. By continuously transporting the electrophotographic photosensitive member, an electrophotographic photosensitive member excellent in film thickness uniformity can be obtained with a comprehensively high adhesion efficiency.
[0055]
Examples of the spiral coating method include a method using a liquid injection coating machine or a curtain coating machine disclosed in Japanese Patent Laid-Open No. 52-119651, and paint from a minute opening disclosed in Japanese Patent Laid-Open No. 1-2231966. There are a method of continuously flying in a streak shape, a method using a multi-nozzle body disclosed in JP-A-3-193161, and the like.
[0056]
Moreover, the following procedures are mentioned as an example of the dip coating method.
First, using a charge transport material (preferably the aforementioned compound), a binder, a solvent, etc., a suitable total solid concentration is 25% or more, more preferably 40% or less, and the viscosity is usually 50 centipoise to 300 centipoise. In the following, a coating solution for forming a charge transport layer, preferably 100 centipoise to 200 centipoise or less, is prepared.
[0057]
Here, the viscosity of the coating solution is substantially determined by the type and molecular weight of the binder polymer, but if the molecular weight is too low, the mechanical strength of the polymer itself is reduced, so that the binder polymer has a molecular weight that does not impair this. Is preferably used. A charge transport layer is formed by a dip coating method using the coating solution thus adjusted.
[0058]
Thereafter, the coating film is dried, and the drying temperature time may be adjusted so that necessary and sufficient drying is performed. A drying temperature is 100-250 degreeC normally, Preferably it is 110-170 degreeC, More preferably, it is the range of 120-140 degreeC.
As a drying method, a hot air dryer, a steam dryer, an infrared dryer, a far infrared dryer, or the like can be used.
[0059]
The photoreceptor formed in this way also has improved electrical and mechanical properties, such as an undercoat layer, a barrier layer, an adhesive layer, an intermediate layer such as a blocking layer, a transparent insulating layer, or a protective layer, if necessary. Needless to say, a layer may be provided. The undercoat layer is usually used between the photosensitive layer and the conductive support, and a commonly used known layer can be used. As the undercoat layer, inorganic fine particles such as titanium oxide, aluminum oxide, zirconia, silicon oxide, organic fine particles, polyamide resin, phenol resin, melamine resin, casein, polyurethane resin, epoxy resin, cellulose, nitrocellulose, polyvinyl alcohol, polyvinyl butyral Ingredients such as resins can be used. These fine particles and resins can be used alone or in admixture of two or more. The thickness of the undercoat layer is usually 0.01 to 50 μm, preferably 0.01 to 10 μm.
[0060]
A known blocking layer may be provided between the photosensitive layer and the conductive support. When a surface protective layer is provided on the photoreceptor, the thickness of the protective layer can be 0.01 to 20 μm, preferably 0.1 to 10 μm.
The binder can be used for the protective layer, but may contain a conductive material such as the charge generator, charge transport agent, additive, metal, metal oxide, or the like. The addition amount of the wax can be 0.01 to 30% by weight, and preferably 0.1 to 10% by weight.
[0061]
Further, the photosensitive layer of the electrophotographic photoreceptor of the present invention is a known plasticizer, antioxidant, ultraviolet ray for improving the film formability, flexibility, coatability, mechanical strength, film formability, durability and the like. An absorbent and a leveling agent may be contained.
<Multilayer photoconductor>
Charge generation layer The charge generation layer forming the laminated photosensitive layer of (1) and (2) described above is composed of a binder resin and other organic photoconductive compounds, dyes, and electrons as required. The charge generation layer is obtained by dissolving or dispersing in a solvent together with an attractive compound and coating and drying the coating solution thus obtained.
[0062]
The charge generation material is usually dispersed and dissolved in an appropriate dispersion medium using a ball mill, ultrasonic disperser, paint shaker, attritor, sand grinder, etc., and a binder resin is added as necessary to adjust the coating solution. The liquid is applied by a coating method such as a dipping method, a spray method, a bar coater method, a blade method, a roll coater method, a wire bar coating method, or a knife coater coating method, and then dried. The charge generation layer may be formed by depositing the charge generation material by a vapor deposition method such as vapor deposition or sputtering.
[0063]
Specifically, the fine particles of the charge generation material are, for example, polyester resin, polyvinyl acetate, polyester, polycarbonate, polyvinyl acetoacetal, polyvinyl propional, polyvinyl butyral, phenoxy resin, epoxy resin, urethane resin, cellulose ester, cellulose ether, and the like. You may use with the dispersion layer of the form bound by various binder resin. Further, examples of the binder resin include polymers and copolymers of vinyl compounds such as styrene, vinyl acetate, vinyl chloride, acrylic acid ester, methacrylic acid ester, vinyl alcohol, and ethyl vinyl ether, polyamide, and silicon resin. In this case, the charge generation material (charge generation material) is used in an amount of usually 5 to 500 parts by weight, preferably 20 to 300 parts by weight with respect to 100 parts by weight of the binder resin, and the film thickness of the charge generation layer is usually 0.01. ˜5 μm, preferably 0.05-2 μm, more preferably 0.15-0.8 μm. In addition, the charge generation layer may contain various additives such as a leveling agent, an antioxidant, and a sensitizer for improving the coating property as necessary. Furthermore, the charge generation layer may be a vapor deposition film of the charge generation material.
-Charge transport layer As described above, the charge transport material is used.
[0064]
As the binder resin used in the charge transport layer, in addition to the above-described polyester resin of the present invention, for example, vinyl polymers such as polymethyl methacrylate, polystyrene, polyvinyl chloride, and copolymers thereof, polycarbonate, polyester, Polyester carbonate, polysulfone, polyimide, phenoxy, epoxy, silicone resin, etc. can be shared or copolymerized, and these partially crosslinked cured products can also be used.
[0065]
The ratio of the binder resin to the charge transport material is usually 10 to 200 parts by weight, preferably 30 to 150 parts by weight, based on 100 parts by weight of the binder resin.
The thickness of the charge transport layer is usually 10 to 50 μm, preferably 13 to 35 μm.
[0066]
Furthermore, the charge transport layer may contain various additives such as an antioxidant, an electron withdrawing compound, a sensitizer, and other charge transport materials as necessary.
In addition, various additives for improving the mechanical strength and durability of the coating film can be used. Examples of such additives include known plasticizers, various stabilizers, fluidity imparting agents, and crosslinking agents.
Forming method of photosensitive layer In the case of a photosensitive layer comprising two layers of a charge generation layer and a charge transport layer, the charge transport layer obtained by coating the coating solution on the charge generation layer or coating the coating solution It can be manufactured by forming a charge generation layer on the substrate.
[0067]
Solvents for preparing the coating solution include ethers such as tetrahydrofuran and 1,4-dioxane, ketones such as methyl ethyl ketone and cyclohexanone; aromatic hydrocarbons such as toluene and xylene; N, N-dimethylformamide, acetonitrile, N-methyl Examples include aprotic polar solvents such as pyrrolidone and dimethyl sulfoxide; esters such as ethyl acetate, methyl formate and methyl cellosolve acetate; and solvents that dissolve amine compounds such as chlorinated hydrocarbons such as dichloroethane and chloroform. Of course, it is necessary to select one that dissolves the binder.
[0068]
The photoreceptor formed in this manner also includes layers for improving electrical and mechanical properties, such as an intermediate layer such as a barrier layer, an adhesive layer, and a blocking layer, a transparent insulating layer, or a protective layer, if necessary. Needless to say, it may have.
As the outermost surface layer, a conventionally known overcoat layer mainly composed of, for example, a thermoplastic or thermosetting polymer may be provided.
[0069]
As a method for forming each layer, a known method such as sequential application of a coating solution obtained by dissolving or dispersing a substance contained in a layer in a solvent can be applied.
<Single layer type photoreceptor>
In the case of the dispersion type photosensitive layer (3) described above, the kind of the charge generating material used is the same as that described above, but the particle size must be sufficiently small, preferably 1 μm or less, more preferably Is used at 0.5 μm or less.
[0070]
The amount of the charge generating material dispersed in the photosensitive layer is, for example, in the range of 0.5 to 50% by weight. However, if the amount is too small, sufficient sensitivity cannot be obtained, and if it is too large, the chargeability is lowered and the sensitivity is lowered. More preferably, it is used in the range of 1 to 20% by weight.
A single-layer type photosensitive layer is prepared by dissolving the above-described charge transporting substance together with the above-described binder resin in an appropriate solvent according to a conventional method, and, if necessary, an appropriate charge-generating material, sensitizing dye, electron-withdrawing compound, A coating liquid obtained by adding other charge transporting materials or known additives such as plasticizers and pigments is coated on a conductive support and dried, usually several μ to several tens μ, preferably It can be produced by forming a layer having a thickness of 10 to 45 μm, particularly preferably 20 μm or more.
<Electrophotographic photoreceptor>
The electrophotographic photoreceptor thus obtained is a photoreceptor that maintains excellent printing durability over a long period of time, and is suitable for the electrophotographic field such as copying machines, printers, fax machines, and plate making machines.
[0071]
In using the electrophotographic photosensitive member of the present invention, a corona charger such as corotron or scorotron, a contact charger such as a charging roll or a charging plus, etc. are used as the charger. The exposure is performed using a halogen lamp, a fluorescent lamp, a laser (semiconductor, He—Ne), an LED, a photoreceptor internal exposure system, or the like. In the development process, a dry development method such as cascade development, one-component insulating toner development, one-component conductive toner development, two-component magnetic brush development, or the like is used.
[0072]
For the transfer process, electrostatic transfer methods such as corona transfer, roller transfer, and belt transfer, pressure transfer methods, and adhesive transfer methods are used. For fixing, heat roller fixing, flash fixing, oven fixing, pressure fixing, or the like is used. For cleaning, brush cleaner, magnetic brush cleaner, electrostatic brush cleaner, magnetic roller cleaner, blade cleaner, etc. are used.
[0073]
【Example】
EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to these examples as long as the gist of the present invention is not exceeded.
In the examples, “parts” means “parts by weight”.
Example 1
<Manufacture of photoconductor>
10 parts by weight of Y-type oxytitanium phthalocyanine exhibiting a maximum diffraction peak at a Bragg angle (2θ ± 0.2) of 27.3 ° in X-ray diffraction by CuKα rays, and 150 parts by weight of 4-methoxy-4-methylpentanone-2 In addition to the above, pulverization and dispersion treatment was performed with a sand grind mill.
[0074]
In addition, 5% of 5% 1,2-dimethoxyethane solution of polyvinyl butyral (trade name Denkabutyral # 6000C, manufactured by Denki Kagaku Kogyo Co., Ltd.) and 5% of phenoxy resin (trade name PKHH, manufactured by Union Carbide) 1, A binder solution was prepared by mixing 100 parts of a 2-dimethoxyethane solution.
100 parts by weight of the binder solution and an appropriate amount of 1,2-dimethoxyethane were added to 160 parts by weight of the previously prepared pigment dispersion to finally prepare a dispersion having a solid content concentration of 4.0%.
[0075]
On the polyethylene terephthalate film on which the dispersion liquid obtained in this manner is vapor-deposited on the surface, or on the aluminum base tube for toner filming evaluation by an actual machine test described later, the film thickness is 0.4 μm. The charge generation layer was provided by coating.
Next, on this film, a 70:30 copolymer of 60 parts of the charge transporting compound (2) in Table-2 and the polyesters (P-1) and (M-1) shown in Table-1 ( (Viscosity average molecular weight 35000) A solution prepared by dissolving 100 parts by weight of a tetrahydrofuran / toluene mixed solution (560 parts by weight) is applied by a film applicator in the case of a sheet, and is applied by dip coating in the case of a drum. A photoconductor was prepared by providing a charge transport layer so as to have a thickness of 25 μm.
<Evaluation of electrical characteristics of photoconductor>
Next, the sheet-like electrophotographic photosensitive member is mounted on a photosensitive member characteristic measurement [Model EPA8100 manufactured by Kawaguchi Electric Co., Ltd.], charged to have a current flowing into the aluminum surface of 35 μA, and then exposed and neutralized. The half exposure amount (E _1/2 ) and the residual potential (Vr) at that time were measured. The results are shown in Table-3.
[Friction test]
The toner is uniformly placed on the sheet-shaped photoconductor prepared above so as to have a concentration of 0.1 mg / cm ^2, and a urethane rubber having a thickness of 2 mm made of the same material as the cleaning blade is cut into a 1 cm width on the contact surface. Was contacted at an angle of 45 degrees, and the dynamic friction coefficient was measured with a fully automatic friction and wear tester DFPM-SS manufactured by Kyowa Interface Chemical Co., Ltd. under the conditions of a load of 200 g, a speed of 5 mm / sec, a stroke of 20 mm, and a repetition count of 100 times. . The results are shown in Table-3.
[Abrasion test]
The sheet-like photoreceptor film was cut into a circle having a diameter of 10 cm, and the wear was evaluated by a Taber abrasion tester (manufactured by Toyo Seiki Co., Ltd.). Test conditions were measured by comparing the weight before and after the test with 1000 wheels without load (the weight of the wear wheel) under the atmosphere of 23 ° C. and 50% RH and without wear (self-weight of the wear wheel). did. The results are shown in Table-3.
[Gas resistance test]
The sheet-like photoreceptor film was measured for the surface resistance value of the photoreceptor before and after exposure to a NOx atmosphere at a concentration of about 6 ppm for 7.5 hours.
[0076]
Example 2
In Example 1, a photoconductor was prepared and evaluated in the same manner as in Example 1 except that the charge transporting compound (20) was used instead of the charge transporting compound (2) in Table 2. The results are shown in Table-3.
Comparative Example 1
In Example 1, a photoreceptor was prepared and evaluated in the same manner as in Example 1 except that a charge transporting compound having the following structure was used instead of the charge transporting compound (2) in Table-2. The results are shown in Table-3.
[0077]
[Chemical 7]

[0078]
Comparative Example 2
In Example 1, a photoconductor was prepared and evaluated in the same manner as in Example 1 except that instead of the polyester resin, a polycarbonate resin having a viscosity average molecular weight of 31400 was used instead of the polyester resin. The results are shown in Table-3.
[0079]
[Chemical 8]

[0080]
As can be seen from these results, the photoreceptor of the present invention not only has excellent electrical characteristics and mechanical properties, but also has a high surface resistance. Yes, it is difficult to cause image deterioration such as image blur and is advantageous from the viewpoint of high image quality.
[0081]
[Table 26]

[0082]
【The invention's effect】
According to the present invention, there is provided an electrophotographic photosensitive member that has little wear in repeated use over a long period of time, is excellent in cleaning property and durability against scratches, and does not impair other properties such as electrical properties and coating properties.

Claims (4)

In an electrophotographic photoreceptor in which at least a photosensitive layer is formed on a conductive support, the photosensitive layer contains at least a polyester resin and a butadiene-based charge transport material, and the polyester resin is represented by the following general formula (1). (However, the polyester resin is a copolymer in which the dicarboxylic acid structural part has dicarboxylic acid units derived from isophthalic acid and terephthalic acid, and the dicarboxylic acid unit derived from isophthalic acid is all dicarboxylic acid.) The electrophotographic photosensitive member is characterized by being 30% or less with respect to the unit .

(In general formula (1), Ar ₁ and Ar ₂ represent a benzene ring which may have a substituent, X represents a benzene ring which may have a substituent, and R ₁ and R ₂ are respectively (A hydrogen atom, an alkyl group which may have a substituent, an aryl group, or a cyclic alkylidene group in which R ₁ and R ₂ are linked.) In the polyester resin, Ar ₁ and Ar ₂ are represented by the following structure in the general formula (1), and R ₁ and R ₂ are each independently a hydrogen atom or a methyl group, or R ₁ and R ₂ are The electrophotographic photosensitive member according to claim 1 , which is integrally formed with a cyclohexyl group.

(In the general formula (2), R _{3 to} R ₆ each independently represents a hydrogen atom or a lower alkyl group having 5 or less carbon atoms.) The electrophotographic photosensitive member according to claim 1, wherein the butadiene-based charge transporting material has a structure represented by the following general formula (3).

(In the general formula (3), X ₁ ~X ₄ represents an aryl group which may have a substituent.)   In the polyester resin having the structural unit represented by the general formula (1), the ratio of the copolymerization ratio of dicarboxylic acid units derived from isophthalic acid to all dicarboxylic acid units is 10 to 30%, The electrophotographic photosensitive member according to claim 1.