JPH0627724A - Positively charged one-component developer - Google Patents

Positively charged one-component developer

Info

Publication number
JPH0627724A
JPH0627724A JP4099237A JP9923792A JPH0627724A JP H0627724 A JPH0627724 A JP H0627724A JP 4099237 A JP4099237 A JP 4099237A JP 9923792 A JP9923792 A JP 9923792A JP H0627724 A JPH0627724 A JP H0627724A
Authority
JP
Japan
Prior art keywords
developer
positively charged
toner
component developer
weight
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
JP4099237A
Other languages
Japanese (ja)
Other versions
JP2819935B2 (en
Inventor
Yasuhito Yuasa
安仁 湯浅
Noriaki Hirota
典昭 廣田
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP4099237A priority Critical patent/JP2819935B2/en
Publication of JPH0627724A publication Critical patent/JPH0627724A/en
Application granted granted Critical
Publication of JP2819935B2 publication Critical patent/JP2819935B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To provide a positively charged one-component developer with stable fixing properties and excellent offset resistance and stress resistance by using a specific crosslinked polymer as binding resin, providing a quaternary ammonium salt as a charge control agent by a specific amount, and adding a specific fluidizer. CONSTITUTION:A positively charged one-component developer comprises binding resin, colorant, a charge control agent and a fluidizer. The binding resin is a copolymer of formulae I-III, i.e., a crosslinked polymer with melt viscosity at 130 deg.C and 160 deg.C being 1X10<5> to 1X10<7> poise and 1X10<4> to 1X10<6> poise, respectively; the charge control agent is composed of a quaternary ammonium salt and is contained in the developer by 0.05 to 5.0wt%; the fluidizer is prepared by addition of positively charged silica and negatively charged silica in the ratio of 9:1 to 5:5 to the developer by 0.01 to 3.0wt.%. In the formulae, R1 represents H, CH3, R2 represents H, a C1-10 alkyl group, R3 represents CnH2n (n is l to 5), and R4 represents a C1-5 alkyl group.

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、靜電印刷や、
靜電記録などに用いられる一成分現像剤に関するもので
ある。
BACKGROUND OF THE INVENTION The present invention relates to electrophotography, electronic printing,
The present invention relates to a one-component developer used for electrostatic recording and the like.

【0002】[0002]

【従来の技術】従来、電子写真法としては米国特許第2
297691明細書、特公昭42ー23910号公報、
及び特公昭43ー24748号公報等で多種の方法が記
載されている。一般には光導電性物質を利用して種々の
光学手段により感光体上に電気的靜電潜像を形成し、つ
いでこの靜電潜像を現像剤(以下トナ−と称する)を用
い可視像化し、必要に応じて紙等に転写したのち、加熱
あるいは圧力等により定着し、コピー画像を得るもので
ある。
2. Description of the Related Art Conventionally, US Pat.
297691 specification, Japanese Patent Publication No. 42-23910,
Also, various methods are described in Japanese Examined Patent Publication No. 43-24748 and the like. Generally, a photoconductive substance is used to form an electric latent electrostatic image on a photoconductor by various optical means, and then the latent electrostatic image is visualized by using a developer (hereinafter referred to as toner). If necessary, it is transferred onto paper or the like and then fixed by heating or pressure to obtain a copy image.

【0003】電気的潜像をトナ−を用いて可視像化する
方法として、米国特許第2874063号明細書に記載
されている磁気ブラシ法、同第2618552明細書に
記載されているカスケード現像法及び米国特許第290
9258明細書に記載されている導電性の磁性トナ−を
用いる方法など種々知られている。
As a method of visualizing an electric latent image by using a toner, a magnetic brush method described in US Pat. No. 2,870,633 and a cascade developing method described in US Pat. No. 2,618,552 are disclosed. And U.S. Pat. No. 290
Various methods such as a method using a conductive magnetic toner described in the specification of 9258 are known.

【0004】また現像方法としては、おもに、キャリア
と呼ばれる鉄粉や、ガラスビーズ粒子等とトナーとを混
合したものを現像剤として用いる二成分現像方法と、ト
ナー単独で現像剤として用いる一成分現像方式がある。
これらに用いられるトナ−は種々の物理的および化学的
特性を要求される。
The developing method is mainly a two-component developing method in which iron powder called carrier, a mixture of glass bead particles and the like and a toner are used as a developer, and a one-component developing method in which the toner alone is used as a developer. There is a method.
The toners used in these are required to have various physical and chemical properties.

【0005】前者の二成分現像方法はトナーおよびキャ
リアを混合攪拌して相互の摩擦帯電によりトナーを帯電
させる現像方法であるため、帯電性,搬送性は安定す
る。しかしこの方法はトナーが逐次消費されるため、ト
ナーとキャリアの比を常に一定に維持する必要があり、
トナー濃度調節機能が必要になり、小型,軽量化が困難
である。
The former two-component developing method is a developing method in which the toner and the carrier are mixed and stirred, and the toner is charged by mutual frictional charging, so that the charging property and the transporting property are stable. However, this method consumes toner one after another, so it is necessary to keep the ratio of toner and carrier constant.
The toner density adjustment function is required, and it is difficult to reduce the size and weight.

【0006】小型、軽量が可能になる後者の一成分現像
方法には磁気の力を利用して、トナーを搬送する磁性一
成分の現像方法が考案されている。またマグネットロー
ラを用いないより小型軽量化が可能になる現像剤担持ロ
ーラメンバのみで一成分現像剤の帯電,搬送,供給を行
なう非磁性一成分現像方法が考え出されている。特にこ
れは磁性を用いないためカラー現像用として使用される
例もある。
In the latter one-component developing method which enables downsizing and weight reduction, a magnetic one-component developing method for conveying toner by utilizing magnetic force has been devised. In addition, a non-magnetic one-component developing method has been devised, in which the one-component developer is charged, conveyed, and supplied only by the developer-carrying roller member, which can be made smaller and lighter than a magnet roller. In particular, since it does not use magnetism, it is used for color development in some cases.

【0007】周知のようにこれらの現像法に使用される
靜電荷現像用のトナ−は一般的に樹脂成分、顔料もしく
は染料からなる着色成分及び可塑剤、電荷制御剤等の添
加成分によって構成されている。樹脂成分として天然ま
たは合成樹脂が単独あるいは適時混合して使用されてい
る。
As is well known, the toner for electrostatic charge development used in these developing methods is generally composed of a resin component, a coloring component composed of a pigment or a dye, and an additive component such as a plasticizer and a charge control agent. ing. As the resin component, natural or synthetic resins are used alone or in a proper mixture.

【0008】しかしながら近年複写像の益々の高画質化
や画質の長期安定性が望まれる傾向が著しくなるにつ
れ、トナ−の主要構成成分である結着樹脂に従来以上の
定着性帯電性や耐久性が要求されている。特公昭51ー
23354号公報、特公昭63ー39052号公報、特
公昭63ー42252号公報、特公昭63ー49221
号公報、特公昭63ー52375号公報、特公平1ー1
7579号公報には結着樹脂として架橋された重合体を
用いたトナ−が提案され、良好な定着性と耐衝撃性に優
れており、耐久性の良いトナ−を提供している。また特
開昭54−143647号公報では添加剤なしのアミノ
基含有電子写真トナーを提案し、安定な帯電特性のトナ
ーを提供している。
However, as the tendency toward higher image quality of copied images and long-term stability of image quality has become remarkable in recent years, the binder resin, which is a main constituent component of the toner, has a fixing property higher than that of conventional toners and durability. Is required. JP-B-51-23354, JP-B-63-39052, JP-B-63-42252, JP-B-63-49221
Japanese Patent Publication, Japanese Patent Publication No. 63-52375, Japanese Patent Publication No. 1-1
Japanese Patent No. 7579 proposes a toner using a cross-linked polymer as a binder resin, and provides a toner having excellent fixability and impact resistance and excellent durability. Further, Japanese Patent Application Laid-Open No. 54-143647 proposes an electrophotographic toner containing an amino group containing no additive, and provides a toner having stable charging characteristics.

【0009】[0009]

【発明が解決しようとする課題】しかしながら上記の構
成では以下のような問題点を有している。
However, the above configuration has the following problems.

【0010】加熱によりよって容易に溶融するトナ−の
多くは貯蔵中や複写機の現像器内でケーキ化や凝集が起
こり易い。また多くのトナーでは長期の連続使用による
繰り返しの現像により、トナー粒子が現像器内の部材と
の衝突、また層規制部材からのストレス等により衝撃を
受け、トナー粒子が劣化し、得られる画像濃度が低下
し、あるいは背景濃度が増大し、複写画像の品質を低下
させる。
Many toners that are easily melted by heating are likely to be caked or aggregated during storage or in the developing unit of a copying machine. Also, with many toners, due to repeated development due to long-term continuous use, the toner particles collide with members in the developing device and are impacted by stress from the layer regulation member, etc., and the toner particles deteriorate, resulting in image density Or the background density is increased, and the quality of the copied image is deteriorated.

【0011】これらの望ましくない現象はトナ−粒子の
脆さに起因するところが多い。即ち現像剤の寿命に関係
するところのものであり、特に現像器中でトナ−粒子は
靜電潜像と対面した現像領域に搬送されるまでに現像剤
担持ローラメンバ、層規制ブレード、現像ローラ等から
かなりのストレスを受ける。このストレスによりトナ−
粒子が破壊され微粉粒子が増加したり、樹脂表面に外添
処理された疎水性シリカ粒子が樹脂中へ打ち込まれたり
して、トナ−粒子が劣化し、現像特性が低下してしま
う。このような劣化現象を回避する為に上記のような架
橋性の高分子量重合体を用いることが提案されている
が、単に架橋しただけだは複写の最終工程である熱定着
工程で定着温度が上昇し、より多くの熱量を必要とす
る。また架橋された高粘度タイプの重合体では顔料を樹
脂中へ混練分散させるとき充分には良好に分散し難いこ
とから架橋された重合体を結着樹脂とするトナ−は良好
な現像特性を得ることが難しいという欠点を有してい
る。それに対して架橋重合体と別な樹脂を混合させこれ
らの課題を改善しようと試みているが、それだけではま
だ充分な分散性は得られない。これは架橋重合体のよう
な高粘度の樹脂では混練時に樹脂と顔料等の内添剤との
濡れ性が妨げられるためである。
These undesired phenomena are often due to the brittleness of toner particles. That is, it relates to the life of the developer. In particular, the toner particles in the developing device are transported to the developing area facing the electrostatic latent image by the developer carrying roller member, layer regulating blade, developing roller, etc. Receive a lot of stress from. This stress causes the toner
The particles are destroyed and the number of fine powder particles is increased, or the hydrophobic silica particles externally treated on the resin surface are driven into the resin, so that the toner particles are deteriorated and the developing characteristics are deteriorated. In order to avoid such a deterioration phenomenon, it has been proposed to use the above-mentioned crosslinkable high molecular weight polymer. However, if the crosslinking temperature is simply crosslinked, the fixing temperature is increased in the heat fixing step which is the final step of copying. Rise and need more heat. Further, in a crosslinked high-viscosity type polymer, when the pigment is kneaded and dispersed in the resin, it is difficult to sufficiently disperse the pigment sufficiently. Therefore, a toner using the crosslinked polymer as a binder resin obtains good developing characteristics. It has the drawback of being difficult. On the other hand, attempts have been made to improve these problems by mixing a cross-linked polymer with another resin, but this alone cannot provide sufficient dispersibility. This is because a high-viscosity resin such as a crosslinked polymer impedes the wettability between the resin and an internal additive such as a pigment during kneading.

【0012】顔料等の内添剤の分散が悪いとき、長期使
用時に分散が良好な粒子が現像に使用され、分散の悪い
粒子が現像器内に残留する選択現像が生じ、これがトナ
−特性の劣化を引き起こす。
When the internal additives such as pigments are poorly dispersed, particles having good dispersion are used for development during long-term use, and particles having poor dispersion remain in the developing device for selective development, which is a toner property. Cause deterioration.

【0013】また上記構成では帯電性が重要視される一
成分現像においては上記構成材料では負帯電性が強くな
る傾向にあり、正帯電性の一成分現像には十分な帯電量
が得られない状況にある。そのため正帯電電荷制御剤の
添加量を増やして、正帯電性を高める手法が取られる
が、これでは電荷制御剤等の内添剤の分散性が悪くなり
帯電分布がブロードになり、現像特性が悪化する要因と
なる。
Further, in the one-component development in which the chargeability is important in the above-mentioned constitution, the negative chargeability tends to become strong in the above-mentioned constituent materials, and a sufficient charge amount cannot be obtained for the positively-charged one-component development. There is a situation. Therefore, a method of increasing the positive chargeability by increasing the addition amount of the positive charge control agent is used, but with this, the dispersibility of the internal additive such as the charge control agent is deteriorated, the charge distribution becomes broad, and the developing characteristics are It becomes a factor to worsen.

【0014】またトナーの流動性を上げるために、最終
行程でシリカ等の微粉末を外添加処理される。この時使
用されるシリカはヘキサメチレンジシラザン、ジメチル
ジクロロシラン等で疎水化処理されたものが多く用いら
れるが、これらはトナーの流動性を高めるのに良好な特
性を示すが、負帯電性が強く表れる傾向にあり正帯電性
トナーには不向きである。叉アミノシラン等で処理され
た正帯電性のシリカでは凝集し易く、耐湿性に難があ
り、高い流動性が要求される一成分現像には問題があ
る。
Further, in order to improve the fluidity of the toner, fine powder such as silica is externally added in the final step. Many silicas used at this time are hydrophobized with hexamethylenedisilazane, dimethyldichlorosilane and the like. These show good characteristics for enhancing the fluidity of the toner, but have negative chargeability. It tends to appear strongly and is not suitable for positively charged toner. In addition, positively-charged silica treated with aminosilane or the like easily aggregates, has difficulty in moisture resistance, and has a problem in one-component development that requires high fluidity.

【0015】本発明は上記問題点に鑑み、安定な定着
性、耐オフセット性、耐ストレスに優れており、凝集を
起こさず、流動性にも優れており、また顔料等の内添剤
を良好に分散でき、正帯電性の一成分現像においても高
帯電の正帯電が得られ現像性が安定し、画像濃度が高く
カブリのない安定した正帯電一成分現像剤を提供するこ
とを目的とする。
In view of the above problems, the present invention is excellent in stable fixing property, anti-offset property and stress resistance, does not cause agglomeration and is excellent in fluidity, and has good internal additives such as pigments. The present invention aims to provide a stable positively charged one-component developer which can be dispersed in a high-charged state, can obtain a high-charged positive charge even in the positively-charged one-component development, has stable developability, has a high image density, and has no fog. .

【0016】[0016]

【課題を解決するための手段】この目的を達成するため
に本発明は耐ストレス性の強い架橋重合体を使用し、そ
れに正帯電性の強い官能基を有するモノマーを共重合さ
せる。更に帯電の立ち上がりをよくするために第4級ア
ンモニウム塩を添加する。さらに正帯電性の疎水性シリ
カと負帯電性の疎水性シリカの混合物を外添加する。こ
の構成により正帯電性と定着性と流動性と耐ストレス性
を同時に満足する事が可能になる。
In order to achieve this object, the present invention uses a crosslinked polymer having a strong stress resistance, and a monomer having a functional group having a strong positive charging property is copolymerized therewith. Further, a quaternary ammonium salt is added in order to improve the rise of charging. Furthermore, a mixture of positively charged hydrophobic silica and negatively charged hydrophobic silica is externally added. With this configuration, it becomes possible to simultaneously satisfy positive charging property, fixing property, fluidity and stress resistance.

【0017】即ち、本発明の正帯電一成分現像剤は静電
潜像を担持するための静電潜像担持体と、現像剤を収容
するための現像剤ホッパーと、現像剤を摩擦帯電させな
がら担持搬送する現像剤担持ローラメンバーと、静電潜
像に対面した現像域へ現像剤を搬送させる現像ローラ
と、現像剤を層規制し、薄層化する弾性部材を具備する
現像装置に用いる正帯電一成分現像剤であって、正帯電
一成分現像剤が少なくとも結着樹脂、着色剤、電荷制御
剤、流動化剤から構成され、結着樹脂が少なくとも一般
式(化1)、(化2)、(化3)からなる共重合体で、
かつ130℃における溶融粘度が1×105〜1×107
(poise)で、160℃における溶融粘度が1×104〜1
×106(poise)で架橋剤の存在下で重合して得られる架
橋重合体であり、かつ電荷制御剤が少なくとも第4級ア
ンモニウム塩で構成され、第4級アンモニウム塩が正帯
電一成分現像剤重量に対し0.05〜5.0重量%含有し、か
つ流動化剤が正帯電性シリカと負帯電性シリカを9:1
〜5:5の割合で正帯電一成分現像剤重量に対し0.01〜
3.0重量%外添加処理したものである。
That is, the positively charged one-component developer of the present invention is an electrostatic latent image carrier for carrying an electrostatic latent image, a developer hopper for containing the developer, and the developer is frictionally charged. Used in a developing device including a developer carrying roller member for carrying and carrying the developer, a developing roller for carrying the developer to a developing area facing the electrostatic latent image, and an elastic member for layer-regulating and thinning the developer. A positively charged one-component developer, wherein the positively charged one-component developer is composed of at least a binder resin, a colorant, a charge control agent, and a fluidizing agent, and the binder resin is at least one of the general formulas (Chemical Formula 1) and (Chemical Formula 1 2), a copolymer of (Chemical Formula 3),
And the melt viscosity at 130 ° C. is 1 × 10 5 to 1 × 10 7
(poise), the melt viscosity at 160 ° C. is 1 × 10 4 to 1
It is a cross-linked polymer obtained by polymerizing at 10 6 (poise) in the presence of a cross-linking agent, and the charge control agent is composed of at least a quaternary ammonium salt, and the quaternary ammonium salt is a positively charged one-component development. 0.05 to 5.0% by weight based on the weight of the agent, and the fluidizing agent contains 9: 1 positively charged silica and negatively charged silica.
〜5: 5 0.01 to 0.01 weight of positively charged one-component developer
3.0% by weight external addition treatment.

【0018】[0018]

【化4】 [Chemical 4]

【0019】[0019]

【化5】 [Chemical 5]

【0020】[0020]

【化6】 [Chemical 6]

【0021】以下本発明を詳細に説明する。本発明の一
成分現像剤の結着樹脂はビニル系単量体を重合または共
重合したビニル系重合体である。この結着樹脂成分の架
橋重合体を構成する単量体のスチレンとしては例えばス
チレン、αーメチルスチレン、Pークロルスチレンなど
のスチレン及びその置換体、アクリル酸アルキルエステ
ルとしては、例えばアクリル酸、アクリル酸メチル、ア
クリル酸エチル、アクリル酸ブチル、アクリル酸ドデシ
ル、アクリル酸オクチル、アクリル酸イソブチル、アク
リル酸イソブチル、アクリル酸ヘキシル、アクリル酸フ
ェニル、メタクリル酸アルキルエステルとしては、例え
ばメタクリル酸、メタクリル酸メチル、メタクリル酸エ
チル、メタクリル酸ブチル、メタクリル酸オクチル、メ
タクリル酸イソブチル、メタクリル酸ドデシル、メタク
リル酸ヘキシル、などの二重結合を有するモノカルボン
酸及びその置換体等がある。
The present invention will be described in detail below. The binder resin of the one-component developer of the present invention is a vinyl polymer obtained by polymerizing or copolymerizing a vinyl monomer. Examples of the monomer styrene constituting the crosslinked polymer of the binder resin component include styrene, α-methylstyrene, styrene such as P-chlorostyrene and its substitution products, and alkyl acrylates such as acrylic acid and methyl acrylate. Ethyl acrylate, butyl acrylate, dodecyl acrylate, octyl acrylate, isobutyl acrylate, isobutyl acrylate, hexyl acrylate, phenyl acrylate, methacrylic acid alkyl esters such as methacrylic acid, methyl methacrylate, ethyl methacrylate. , Butyl methacrylate, octyl methacrylate, isobutyl methacrylate, dodecyl methacrylate, hexyl methacrylate, and the like, and monocarboxylic acids having a double bond and substituted products thereof.

【0022】また本発明の架橋重合体はおもにモノマー
の重量に対して0.1〜10 重量%の架橋剤モノマーを含む
ビニル系モノマーから合成される重合体であり、架橋剤
としては重合性の二重結合を2個以上持つ化合物で例え
ばジビニルベンゼン、ジビニルナフタレン、等の芳香族
ジビニル化合物、エチレングリコール、テトラエチレン
グリコール、ジメタクリレート等のジエチレン性カルボ
ン酸エステル等がある。
The cross-linked polymer of the present invention is a polymer mainly synthesized from a vinyl-based monomer containing 0.1 to 10% by weight of a cross-linking agent monomer based on the weight of the monomer. Examples of compounds having two or more bonds include aromatic divinyl compounds such as divinylbenzene and divinylnaphthalene, and diethylenic carboxylic acid esters such as ethylene glycol, tetraethylene glycol and dimethacrylate.

【0023】また正帯電性を付与するビニル単量体とし
てはジメチルアミノエチルメタクリレート、ジエチルア
ミノエチルメタクリレート、ジブチルアミノエチルメタ
クリレート、ジメチルアミノエチルアクリレート、ジエ
チルアミノエチルアクリレート、ジブチルアミノエチル
アクリレート等のアミノ基を含有するビニル系単量体が
ある。
Further, the vinyl monomer imparting positive chargeability contains an amino group such as dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, dibutylaminoethyl methacrylate, dimethylaminoethyl acrylate, diethylaminoethyl acrylate, dibutylaminoethyl acrylate. There are vinyl monomers.

【0024】またこれらの共重合体の製造法として塊状
重合、溶液重合、懸濁重合、乳化重合など望みの公知の
重合法が採用され、また触媒はベンゾイルパオキサイ
ド、アゾビスイソブチルニトリルなどの充分なる触媒能
を持つ触媒が用いられる。さらに分子量を調整する目的
で、トリエチルアミン、四塩化炭素、四臭化炭素、n−
ブチルメルカプタンなどの所望の結果を与える連鎖移動
剤を用いることもできる。
As a method for producing these copolymers, desired known polymerization methods such as bulk polymerization, solution polymerization, suspension polymerization and emulsion polymerization are adopted, and the catalyst is sufficient such as benzoyl peroxide, azobisisobutyl nitrile. A catalyst having the following catalytic ability is used. Further, for the purpose of adjusting the molecular weight, triethylamine, carbon tetrachloride, carbon tetrabromide, n-
It is also possible to use a chain transfer agent which gives the desired result, such as butyl mercaptan.

【0025】本発明の架橋重合体は溶融粘度が130℃
において1×105〜1×107(poise)、160℃にお
いて1×104〜1×106(poise)、が好ましい。溶融
粘度特性が130℃で1×107(poise)、160℃で1
×106(poise) 以上になると内添剤の分散性が不均一
になる。また定着時高温の定着温度を必要とするし、粉
砕性が悪化して収率の低下を招く。
The crosslinked polymer of the present invention has a melt viscosity of 130 ° C.
Is preferably 1 × 10 5 to 1 × 10 7 (poise) and 160 ° C. is 1 × 10 4 to 1 × 10 6 (poise). Melt viscosity characteristic is 1 × 10 7 (poise) at 130 ℃, 1 at 160 ℃
When it exceeds × 10 6 (poise), the dispersibility of the internal additive becomes non-uniform. Further, a high fixing temperature is required at the time of fixing, and the pulverizability is deteriorated, resulting in a decrease in yield.

【0026】溶融粘度特性が130℃で1×105(pois
e)、160℃で1×104(poise)以下になると耐ストレ
ス性が低下し、トナー粒子が潜像に導かれる間にストレ
スを受け破砕されたり、シリカの打ち込みにより、流動
性の低下や現像性の悪化につながる。
The melt viscosity characteristic at 130 ° C. is 1 × 10 5 (pois
e) At 160 ° C., when the temperature is 1 × 10 4 (poise) or less, the stress resistance decreases, and the toner particles are crushed by being stressed while being guided to the latent image, and the impact of silica impairs the fluidity. This leads to deterioration of developability.

【0027】このときの溶融粘度測定は高化式フローテ
スター(島津製作所製)で測定し、測定条件はダイズ寸
法1×9mm、押出圧力10kg/cm2で行なった。
The melt viscosity at this time was measured with a Koka type flow tester (manufactured by Shimadzu Corporation), and the measurement conditions were soybean dimension 1 × 9 mm and extrusion pressure 10 kg / cm 2 .

【0028】本発明に使用する架橋重合体は、スチレン
を好ましくは50〜95重量%、成分として含むもので
ある。スチレンの割合が50重量%未満であると、トナ
−の熱溶融性が劣り、定着性が不十分になる。
The crosslinked polymer used in the present invention preferably contains styrene in an amount of 50 to 95% by weight as a component. When the proportion of styrene is less than 50% by weight, the toner has poor heat melting property and insufficient fixing property.

【0029】アミノ基含有単量体の添加量は結着樹脂に
対して0.05〜10重量%が好ましい。0.05重量%以下だと
正帯電性の効果が得られない。また10重量%以上だと
樹脂の重合反応性が低下し、生産効率が悪くなし、また
環境特性も悪化する。
The amount of the amino group-containing monomer added is preferably 0.05 to 10% by weight based on the binder resin. If it is less than 0.05% by weight, the positive charging effect cannot be obtained. If it is 10% by weight or more, the polymerization reactivity of the resin is lowered, the production efficiency is not deteriorated, and the environmental characteristics are deteriorated.

【0030】この単量体を共重合することにより、着色
剤、電荷制御剤等の内添剤の分散性が向上させることが
出来る。これは上記内添剤と樹脂の濡れ性が良くなるた
めと考えている。
By copolymerizing this monomer, the dispersibility of internal additives such as colorants and charge control agents can be improved. It is considered that this is because the wettability between the internal additive and the resin is improved.

【0031】第4級アンモニウム塩の添加量は正帯電一
成分現像剤重量あたり0.1〜10重量%が好ましく、さ
らに0.1〜5重量%が好ましい。これらは使用する現像
方式により当然選択されるものである。添加量が少ない
と帯電の立ち上がりに効果が出ず、多量に添加すると分
散性が低下する。
The amount of the quaternary ammonium salt added is preferably 0.1 to 10% by weight, more preferably 0.1 to 5% by weight, based on the weight of the positively charged one-component developer. These are naturally selected depending on the developing method used. If the addition amount is small, the effect of rising the charging is not exerted, and if the addition amount is large, the dispersibility is deteriorated.

【0032】流動化剤はアミノ化合物等の公知のカップ
リング剤で処理された正帯電疎水性シリカと、ヘキサメ
チレンジシラザン、ジメチルジクロロシラン等の公知の
カップリング剤で処理された負帯電疎水性シリカの混合
物を9:1〜5:5の割合で正帯電一成分現像剤重量に
対し0.01〜3.0重量%外添加処理する。これは正帯電シ
リカによるトナーの正帯電量の確保と負帯電シリカの高
流動特性を引き出すためである。負帯電シリカの混合割
合が低下すると、正帯電シリカの凝集性が顕著に表れ、
流動性が悪化する。特に高湿下において強く見られる。
逆に負帯電シリカの混合割合が増加すると、トナーの正
帯電量が低下し、転写不良、地カブリが目だつようにな
る。シリカの混合物が正帯電一成分現像剤重量に対し0.
01重量%以下になると流動性が低下する。3.0重量%以
上になると浮遊シリカが増加し感光体へのフィルミング
となって表れる。
The fluidizing agent is a positively charged hydrophobic silica treated with a known coupling agent such as an amino compound, and a negatively charged hydrophobic silica treated with a known coupling agent such as hexamethylenedisilazane or dimethyldichlorosilane. The silica mixture is externally added in a proportion of 9: 1 to 5: 5 by 0.01 to 3.0% by weight based on the weight of the positively charged one-component developer. This is to secure the positive charge amount of the toner by the positively charged silica and bring out the high flow property of the negatively charged silica. When the mixing ratio of the negatively charged silica is reduced, the cohesiveness of the positively charged silica is remarkably exhibited,
Liquidity deteriorates. It is strongly seen especially under high humidity.
On the contrary, when the mixing ratio of the negatively charged silica is increased, the positive charge amount of the toner is decreased, and the transfer failure and the background fog are noticeable. A mixture of silica is 0 per weight of positively charged one-component developer.
If it is less than 01% by weight, the fluidity will decrease. If it exceeds 3.0% by weight, the amount of floating silica increases and appears as filming on the photoconductor.

【0033】本発明のトナーの製造方法としては共重合
体と他の内添剤を混合し加熱混練で分散させる。このと
きの加熱混練手法としては公知の加熱混練機を用いて行
なうことが出来る。加熱混練機としては、三本ロール
型、一軸スクリュウー型、二軸スクリュウー型、ハ゛ンハ゛リ
ーミキサー型等の混練物を加熱してせん断力をかけて練る装
置を使用することが出来る。本実験では二軸スクリュー
の池貝鉄工社製のPCM30を使用した。本発明はこれ
に限るものではない。その塊をカッターミル等で粗粉砕
し、その後ジェットミル粉砕機で粉砕され、気流式分級
機で微粉粒子がカットされ、所望の粒度分布を得、シリ
カ等の外添剤を外添処理し、トナ−が得られる。
As the method for producing the toner of the present invention, the copolymer and other internal additives are mixed and dispersed by heating and kneading. As the heating and kneading method at this time, a known heating and kneading machine can be used. As the heating and kneading machine, it is possible to use an apparatus for heating a kneaded material such as a three-roll type, a single-screw type, a twin-screw type, and a banbury mixer type and applying a shearing force to knead the mixture. In this experiment, a twin screw PCM30 manufactured by Ikegai Tekko KK was used. The present invention is not limited to this. The lump is roughly crushed by a cutter mill or the like, then crushed by a jet mill crusher, fine powder particles are cut by an airflow classifier, a desired particle size distribution is obtained, and an external additive such as silica is externally treated. Toner can be obtained.

【0034】本発明に係る正帯電一成分現像剤は前記の
ごとき樹脂を主要成分としているが、このような主要成
分以外に必要に応じて他の公知の重合体を混合して使用
することもできる。例えばエポキシ樹脂、ポリエステル
樹脂、ポリウレタン樹脂等がある。
The positively charged one-component developer according to the present invention has the resin as the main component as described above, but other known polymers may be mixed and used in addition to the main component as required. it can. For example, there are epoxy resin, polyester resin, polyurethane resin and the like.

【0035】また本発明に係る正帯電一成分現像剤には
必要に応じて着色・電荷制御の目的で適当な顔料または
染料が配合される。そのような顔料または染料としては
カーボンブラック、鉄黒、グラファイト、ニグロシン、
アゾ染料の金属錯体、フタロシアニンブルー、セルコオ
イルブルー、デュポンオイルレッド、アニリンブルー、
ベンジジンイエロー、ローズベンガルやこれら等の混合
物があり、電荷量、着色に必要な量が配合される。
If necessary, the positively charged one-component developer according to the present invention may contain an appropriate pigment or dye for the purpose of controlling coloring and charge. Such pigments or dyes include carbon black, iron black, graphite, nigrosine,
Metal complexes of azo dyes, phthalocyanine blue, cerco oil blue, DuPont oil red, aniline blue,
There are benzidine yellow, rose bengal, and mixtures thereof, and the amount of charge and the amount necessary for coloring are blended.

【0036】さらに本発明に係る一成分現像剤は必要に
応じて離型剤が更に配合される。更に必要に応じて他の
種類の添加剤を配合せしめることができる。例えばチタ
ン、アルミナ等の外添剤、酸化スズ、チタン酸ストロン
チウム等の流動性付与剤、研磨剤である。
Further, the one-component developer according to the present invention may further contain a release agent if necessary. Further, other types of additives can be blended if necessary. Examples thereof include external additives such as titanium and alumina, fluidity imparting agents such as tin oxide and strontium titanate, and abrasives.

【0037】さらに本発明に係る正帯電一成分現像剤は
必要に応じて磁性体が配合される。磁性粉としては鉄、
マンガン、ニッケル、コバルト、等の金属粉末や鉄、マ
ンガン、ニッケル、コバルト、亜鉛等のフェライト等が
ある。粉体の平均粒径は10μm以下、特に好ましくは7
μm以下が好ましい。
Further, in the positively charged one-component developer according to the present invention, a magnetic material is blended if necessary. Iron as magnetic powder
Examples include metal powders of manganese, nickel, cobalt, etc., and ferrites of iron, manganese, nickel, cobalt, zinc, etc. The average particle size of the powder is 10 μm or less, particularly preferably 7
μm or less is preferable.

【0038】[0038]

【作用】本発明は上記した構成によって、正帯電性のア
ミノ基含有単量体を共重合することにより、内添剤の均
一分散が図られ、且つ正帯電付与能力が向上し、トナ−
の帯電量分布がシャープになる。また第4級アンモニウ
ム塩を含有させることにより帯電の立ち上がりが向上す
る。また130℃における溶融粘度が1×105〜1×
107(poise)で、160℃における溶融粘度が1×10
4〜1×106(poise) で規定した架橋重合体を使用する
ことにより高い耐ストレス性を確保できる。また流動化
剤に正帯電疎水性シリカと負帯電疎水性シリカを混合外
添することにより正帯電量の確保と、高い流動性の確保
が可能となり、長期連続使用時にも流動性等の低下がな
く、高い正帯電性を維持でき、良好な定着性を示し、画
像濃度が高くカブリのない長期使用時の安定した正帯電
一成分現像剤を提供できる。
According to the present invention, by the above-mentioned constitution, by copolymerizing the positively chargeable amino group-containing monomer, the internal additive is uniformly dispersed, and the positive charge imparting ability is improved.
The charge amount distribution of is sharp. Further, the incorporation of the quaternary ammonium salt improves the rise of charging. Further, the melt viscosity at 130 ° C. is 1 × 10 5 to 1 ×
10 7 (poise), melt viscosity at 160 ℃ 1 × 10
High stress resistance can be secured by using a crosslinked polymer defined by 4 to 1 × 10 6 (poise). In addition, by adding externally mixed positively charged hydrophobic silica and negatively charged hydrophobic silica to the fluidizing agent, it becomes possible to secure a positive charge amount and high fluidity, and the fluidity and the like will not deteriorate even during long-term continuous use. It is possible to provide a stable positively charged one-component developer capable of maintaining high positive chargeability, exhibiting good fixability, high image density, and free from fogging during long-term use.

【0039】[0039]

【実施例】以下本発明の実施例について図面を参照しな
がら説明する。本発明はこれに限定されるものではな
い。
Embodiments of the present invention will be described below with reference to the drawings. The present invention is not limited to this.

【0040】図1は本発明の正帯電一成分現像剤が用い
られる現像装置の一例を示している。現像ローラ1は現
像器2の先端部に一部を露出して設けられ、適当な隙間
を持って感光体ドラムと向いあっている。感光体ドラム
3はアルミニウム等の金属基台の表面に有機光導電性材
料による光導電層を形成したいわゆる有機感光体であ
り、前記有機感光体の表面を帯電した状態で矢印EX
示すように画像露光を行ない、静電潜像を形成する。感
光体ドラムは有機光導電性材料にかぎらずSe,Cd
S,a−Si等の無機光導電性材料でもかまわない。
FIG. 1 shows an example of a developing device in which the positively charged one-component developer of the present invention is used. The developing roller 1 is provided with a part exposed at the tip of the developing device 2, and faces the photosensitive drum with an appropriate gap. The photoconductor drum 3 is a so-called organic photoconductor in which a photoconductive layer made of an organic photoconductive material is formed on the surface of a metal base such as aluminum, and the surface of the organic photoconductor is charged as shown by an arrow E X. The image is exposed to the image to form an electrostatic latent image. The photosensitive drum is not limited to organic photoconductive material, and Se, Cd
An inorganic photoconductive material such as S or a-Si may be used.

【0041】現像ローラ1は現像剤を担持しやすいよう
に表面をサンドブラスト処理されたアルミニウム製金属
ローラ等からなり、現像器2内の現像剤担持ローラメン
バ4(本発明ではファーブラシを使用)によって一成分
現像剤5の供給を受ける。現像ローラはアルミニウム製
に限らず、現像剤を担持搬送しやすいように表面処理さ
れた金属等のローラを用いてもよく、現像剤担持ローラ
メンバはファーブラシに限らずスポンジや金属等の、現
像剤を担持、搬送できるローラ状の部材が用いられても
よい。現像剤担持ローラメンバ(ファーブラシ)4の背
後には現像剤ホッパ6があり、前記現像剤ホッパ6内の
現像剤5は現像剤供給パドル7によって攪拌されなが
ら、現像剤担持ローラメンバ4の側に送り出される。現
像剤担持ローラメンバ4は送り出されてくる現像剤5を
攪拌しながら担持して現像ローラ1の側に搬送し、主と
して現像ローラ1との間で現像剤5を摩擦帯電させなが
ら現像ローラ1に供給する。現像ローラ1は供給された
現像剤5を表面に担持して感光体ドラム3の側に搬送す
る。この搬送途中では現像ローラ1の表面に弾性ブレー
ド8が圧接されている。この弾性ブレード8はウレタン
ゴム、シリコンゴム等のゴムブレードや、適当な金属の
ブレードからなり、現像ローラ1上に供給されている現
像剤5を押圧して所定の層厚を持った一様な薄層に形成
し、感光体ドラム3での静電潜像の現像が安定して行な
われるようにする。この現像のために現像ローラ1には
直流電源9により現像バイアスを印加し、現像ローラ1
上の現像剤5が感光体ドラム3上の静電潜像によく付着
されるようにしている。なお本実施例での現像はいわゆ
る反転現像であるため、現像剤5は感光体ドラム3の画
像露光により電荷の抜けた部分に付着されて顕像を作
る。
The developing roller 1 is composed of an aluminum metal roller or the like whose surface is sandblasted so as to easily carry the developer, and the developer carrying roller member 4 (in the present invention, a fur brush is used) in the developing device 2 is used. The one-component developer 5 is supplied. The developing roller is not limited to aluminum, but may be a roller made of metal or the like that is surface-treated so as to easily carry and convey the developer. The developer carrying roller member is not limited to the fur brush, and may be sponge or metal. A roller-shaped member that can carry and convey the agent may be used. Behind the developer carrying roller member (fur brush) 4, there is a developer hopper 6, and the developer 5 in the developer hopper 6 is agitated by a developer supply paddle 7 while the developer carrying roller member 4 side. Sent to. The developer-carrying roller member 4 carries the sent-out developer 5 while stirring and conveys it to the developing roller 1 side, and mainly to the developing roller 1 while frictionally charging the developer 5 with the developing roller 1. Supply. The developing roller 1 carries the supplied developer 5 on its surface and conveys it to the photosensitive drum 3 side. During this conveyance, the elastic blade 8 is pressed against the surface of the developing roller 1. The elastic blade 8 is made of a rubber blade such as urethane rubber or silicon rubber, or a blade made of a suitable metal, and presses the developer 5 supplied onto the developing roller 1 to form a uniform layer having a predetermined layer thickness. A thin layer is formed so that the electrostatic latent image on the photosensitive drum 3 can be stably developed. For this development, a developing bias is applied to the developing roller 1 by a DC power supply 9, and the developing roller 1
The upper developer 5 is often attached to the electrostatic latent image on the photosensitive drum 3. Since the development in this embodiment is so-called reversal development, the developer 5 is attached to a portion of the photoconductor drum 3 where the charge is removed by image exposure to form a visible image.

【0042】次に現像剤の材料組成および製造方法を述
べる。実施例中の部数はすべて重量部である。また実施
例中のモノマー比はすべて重量%である。
Next, the material composition of the developer and the manufacturing method will be described. All parts in the examples are parts by weight. Further, all the monomer ratios in the examples are% by weight.

【0043】(実施例1)実施例1で使用されるトナ−
a1の材料組成を(表1)に示した。
(Example 1) Toner used in Example 1
The material composition of a1 is shown in (Table 1).

【0044】[0044]

【表1】 [Table 1]

【0045】架橋重合体はスチレン、アクリル酸ブチ
ル、ジメチルアミノメチルメタクリレートモノマーと、
ジビニルベンゼンの架橋剤の存在下で懸濁重合反応で生
成した。(表1)に示した混合物を二軸混練押出機にて
加熱混練し、ジェットミルにて微粉砕を行い、気流分級
機にて微粉をカットし、平均粒径5〜30μmの粒子が
得られた。その後外添処理として上記によってできたト
ナー母体と疎水性シリカをヘンシェルミキサーにて混合
し外添した。最後に振動ふるいにて凝集物を抽出しトナ
ーa1を完成した。このとき外添剤として疎水性シリカは
混合物を1.5重量部外添している。
The cross-linked polymer is styrene, butyl acrylate, dimethylaminomethyl methacrylate monomer,
It was produced by a suspension polymerization reaction in the presence of a divinylbenzene crosslinking agent. The mixture shown in (Table 1) is kneaded by heating with a twin-screw kneading extruder, finely pulverized with a jet mill, and fine powder is cut with an air stream classifier to obtain particles having an average particle size of 5 to 30 μm. It was After that, as a process of external addition, the toner base prepared as described above and the hydrophobic silica were mixed with a Henschel mixer and externally added. Finally, the agglomerates were extracted with a vibrating screen to complete toner a1. At this time, 1.5 parts by weight of the mixture of hydrophobic silica was added as an external additive.

【0046】これをデジタル複写機(松下電器製)「F
P−C1」によって複写テストを10000枚行い、画
像濃度を反射濃度計(マクベス社)で測定し、評価を行
なった。初期画像において反射濃度1.4の高濃度の画像
が得られ、また顔料の分散が良好で凝集物も見られず、
また10000枚後のトナ−の流動性の低下も少なく、
初期の画像に比べて遜色のない高濃度の複写物が得られ
た。(表2)に各トナーの画像濃度の推移を示した。
This is a digital copying machine (Matsushita Electric) "F
A copying test was performed on 10,000 sheets by "P-C1", and the image density was measured by a reflection densitometer (Macbeth Co.) and evaluated. In the initial image, a high-concentration image with a reflection density of 1.4 was obtained, and the pigment dispersion was good and no aggregates were seen,
Also, the decrease in fluidity of the toner after 10,000 sheets is small,
A high-density copy which was comparable to the initial image was obtained. Table 2 shows the transition of the image density of each toner.

【0047】[0047]

【表2】 [Table 2]

【0048】(比較例1)比較例1で使用されるトナー
a2の材料組成を(表3)に示した。
Comparative Example 1 Toner used in Comparative Example 1
The material composition of a2 is shown in (Table 3).

【0049】[0049]

【表3】 [Table 3]

【0050】アミノ基含有単量体を共重合せず、スチレ
ンーアクリル酸ブチルモノマーによる架橋重合体のみを
結着樹脂とし、(表3)に示した混合物を二軸混練押出
機にて加熱混練し、ジェットミルにて微粉砕を行い、気
流分級機にて微粉をカットし、平均粒径5〜30μmの
粒子が得られた。その後外添処理として上記によってで
きたトナー母体と疎水性シリカをヘンシェルミキサーに
て混合し外添した。最後に振動ふるいにて凝集物を抽出
しトナーa2を完成した。このとき外添剤として負帯電疎
水性シリカを1.5重量部外添している。
The amino group-containing monomer was not copolymerized, only the cross-linked polymer of styrene-butyl acrylate monomer was used as the binder resin, and the mixture shown in (Table 3) was heated and kneaded by a twin-screw kneading extruder. Then, fine pulverization was performed with a jet mill, and fine powder was cut with an air stream classifier to obtain particles having an average particle size of 5 to 30 μm. After that, as a process of external addition, the toner base prepared as described above and the hydrophobic silica were mixed with a Henschel mixer and externally added. Finally, the agglomerates were extracted with a vibrating screen to complete toner a2. At this time, 1.5 parts by weight of negatively charged hydrophobic silica is externally added as an external additive.

【0051】これをデジタル複写機(松下電器製)「F
P−C1」によって複写テストを10000枚行い、画
像濃度を反射濃度計(マクベス社)で測定し、評価を行
なった。トナーの正帯電量が低いため初期からの画像濃
度は薄く、また機内のトナー飛散が多く実用的な画像は
得られなかった。また内添剤の分散が悪くカーボンブラ
ックの凝集物が多く観察された。
This is a digital copier (Matsushita Electric) "F
A copying test was performed on 10,000 sheets by "P-C1", and the image density was measured by a reflection densitometer (Macbeth Co.) and evaluated. Since the positive charge amount of the toner was low, the image density was low from the beginning, and the toner was scattered in the machine, so that a practical image could not be obtained. In addition, the dispersion of the internal additive was poor, and many aggregates of carbon black were observed.

【0052】(比較例2)比較例2で使用されるトナ−
a3の材料組成を(表4)に示した。
Comparative Example 2 Toner used in Comparative Example 2
The material composition of a3 is shown in (Table 4).

【0053】[0053]

【表4】 [Table 4]

【0054】比較例のトナーa2の帯電量を実施例1のト
ナーa1にまで帯電量を高めるため比較例1の電荷制御剤
の添加量を6重量%に増加した。(表4)に示した混合
物を二軸混練押出機にて加熱混練し、ジェットミルにて
微粉砕を行い、気流分級機にて微粉をカットし、平均粒
径5〜30μmの粒子が得られた。その後外添処理とし
て上記によってできたトナー母体と疎水性シリカをヘン
シェルミキサーにて混合し外添した。最後に振動ふるい
にて凝集物を抽出しトナーa3を完成した。このとき外
添剤として正帯電疎水性シリカを1.5重量部外添してい
る。
In order to increase the charge amount of the toner a2 of the comparative example to that of the toner a1 of the example 1, the amount of the charge control agent added in the comparative example 1 was increased to 6% by weight. The mixture shown in (Table 4) is kneaded by heating with a twin-screw kneading extruder, finely pulverized with a jet mill, and fine powder is cut with an air stream classifier to obtain particles having an average particle size of 5 to 30 μm. It was After that, as a process of external addition, the toner base prepared as described above and the hydrophobic silica were mixed with a Henschel mixer and externally added. Finally, the agglomerates were extracted with a vibrating screen to complete toner a3. At this time, 1.5 parts by weight of positively charged hydrophobic silica was added as an external additive.

【0055】これをデジタル複写機(松下電器製)「F
P−C1」によって複写テストを10000枚行い、画
像濃度を反射濃度計(マクベス社)で測定し、評価を行
なった。トナーの帯電量は高く得られたが、初期から画
像濃度は低く、複写テスト中にも画像濃度低下が発生
し、実用的な画像は得られなかった。このときトナ−中
の内添剤特に顔料の分散不良が顕著にみられた。また帯
電量分布がブロードになっており、、複写テスト後の現
像器に残留したトナーの粒度分布は大、小粒径成分が見
かけ上多くなっており、選択現像が発生しているため画
像濃度が低下したものと思われる。
This is a digital copying machine (Matsushita Electric) "F
A copying test was performed on 10,000 sheets by "P-C1", and the image density was measured by a reflection densitometer (Macbeth Co.) and evaluated. Although the charge amount of the toner was high, the image density was low from the initial stage, and the image density was lowered during the copying test, and a practical image was not obtained. At this time, the dispersion of the internal additive, especially the pigment, in the toner was remarkably observed. In addition, the charge amount distribution is broad, the particle size distribution of the toner remaining in the developing device after the copy test is large, and the small particle size component is apparently large, so selective development has occurred, so image density Seems to have decreased.

【0056】[0056]

【発明の効果】以上のように本発明は、正帯電性のアミ
ノ基含有単量体を架橋を施した結着樹脂に共重合させ、
電荷制御剤に第4級アンモニウム塩と流動化剤に正帯
電、負帯電疎水性シリカの混合物を用いることにより、
高粘度の架橋重合体を使用しても内添剤の分散の不均一
性が改善され、分散性は向上する。また正帯電性が向上
するとともに、帯電量分布のシャープ化が図られ、帯電
の立ち上がりが向上し、高湿下においても高い流動性を
維持でき、耐ストレス性に優れ、定着性が安定し、長期
連続使用時にも流動性の低下が少なく、画像濃度の高
い、カブリのない安定した、正帯電一成分現像剤が得ら
れる。
As described above, in the present invention, a positively chargeable amino group-containing monomer is copolymerized with a crosslinked binder resin,
By using a mixture of quaternary ammonium salt as the charge control agent and positively and negatively charged hydrophobic silica as the fluidizing agent,
Even when a high-viscosity crosslinked polymer is used, the non-uniformity of the dispersion of the internal additive is improved and the dispersibility is improved. In addition to improving the positive charging property, the distribution of the amount of charge is sharpened, the rising of charging is improved, high fluidity can be maintained even under high humidity, excellent stress resistance, stable fixing property, It is possible to obtain a stable, positively charged one-component developer with high image density, high image density, and low deterioration in fluidity even after long-term continuous use.

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

【図1】本発明の実施例の現像剤が使用される現像機構
の主要部を示す断面図
FIG. 1 is a sectional view showing a main part of a developing mechanism in which a developer according to an embodiment of the present invention is used.

【符号の説明】[Explanation of symbols]

1 現像ローラ 2 現像器本体 3 感光体ドラム 4 現像剤担持ローラメンバ 5 現像剤 6 現像剤収容室 7 現像剤供給パドル 8 弾性ブレード 9 直流電源 1 Developing Roller 2 Developing Device Main Body 3 Photosensitive Drum 4 Developer Holding Roller Member 5 Developer 6 Developer Holding Chamber 7 Developer Supply Paddle 8 Elastic Blade 9 DC Power Supply

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 G03G 9/08 375 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location G03G 9/08 375

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】静電潜像を担持するための静電潜像担持体
と、現像剤を収容するための現像剤ホッパーと、前記現
像剤を摩擦帯電させながら担持搬送する現像剤担持ロー
ラメンバーと、前記静電潜像に対面した現像域へ前記現
像剤を搬送させる現像ローラと、前記現像剤を層規制
し、薄層化する弾性部材を具備する現像装置に用いる正
帯電一成分現像剤であって、前記正帯電一成分現像剤が
少なくとも結着樹脂、着色剤、電荷制御剤、流動化剤か
ら構成され、前記結着樹脂が少なくとも一般式(化
1)、(化2)、(化3)からなる共重合体で、かつ1
30℃における溶融粘度が1×105〜1×107(pois
e)で、160℃における溶融粘度が1×104〜1×1
6(poise)で架橋剤の存在下で重合して得られる架橋重
合体であり、かつ前記電荷制御剤が少なくとも第4級ア
ンモニウム塩で構成され、前記第4級アンモニウム塩が
前記正帯電一成分現像剤重量に対し0.05〜5.0重量%含
有し、かつ前記流動化剤が正帯電性シリカと負帯電性シ
リカを9:1〜5:5の割合で前記正帯電一成分現像剤
重量に対し0.01〜3.0重量%外添加処理することを特徴
とする正帯電一成分現像剤。 【化1】 【化2】 【化3】
1. An electrostatic latent image carrier for carrying an electrostatic latent image, a developer hopper for containing a developer, and a developer carrying roller member for carrying and carrying the developer while frictionally charging the developer. A positively charged one-component developer used in a developing device, which comprises: a developing roller that conveys the developer to a developing area facing the electrostatic latent image; and an elastic member that regulates the layer of the developer and thins the layer. Wherein the positively charged one-component developer is composed of at least a binder resin, a colorant, a charge control agent and a fluidizing agent, and the binder resin is at least one of the general formulas (Chemical formula 1), (Chemical formula 2), (Chemical formula 2), A copolymer of the chemical formula 3), and
Melt viscosity at 30 ° C. is 1 × 10 5 to 1 × 10 7 (pois
e), the melt viscosity at 160 ° C. is 1 × 10 4 to 1 × 1.
It is a cross-linked polymer obtained by polymerizing at 0 6 (poise) in the presence of a cross-linking agent, and the charge control agent is composed of at least a quaternary ammonium salt, and the quaternary ammonium salt is the positively-charged one. 0.05 to 5.0% by weight based on the weight of the component developer, and the fluidizing agent contains positively charged silica and negatively charged silica at a ratio of 9: 1 to 5: 5 with respect to the weight of the positively charged one-component developer. A positively charged one-component developer characterized by being externally added at 0.01 to 3.0% by weight. [Chemical 1] [Chemical 2] [Chemical 3]
JP4099237A 1992-04-20 1992-04-20 Positively charged one-component developer Expired - Fee Related JP2819935B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4099237A JP2819935B2 (en) 1992-04-20 1992-04-20 Positively charged one-component developer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4099237A JP2819935B2 (en) 1992-04-20 1992-04-20 Positively charged one-component developer

Publications (2)

Publication Number Publication Date
JPH0627724A true JPH0627724A (en) 1994-02-04
JP2819935B2 JP2819935B2 (en) 1998-11-05

Family

ID=14242084

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2819935B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1026553A1 (en) * 1999-02-03 2000-08-09 Lexmark International, Inc. Toner composition including positive and negative triboelectric charged hydrophobic extra-particulate additives

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6087059A (en) * 1999-06-28 2000-07-11 Xerox Corporation Toner and developer compositions

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6120053A (en) * 1984-07-06 1986-01-28 Minolta Camera Co Ltd Toner for developing electrostatic latent image
JPS6217751A (en) * 1985-07-16 1987-01-26 Fuji Xerox Co Ltd Developer for electrostatic latent image
JPH01219769A (en) * 1988-02-29 1989-09-01 Canon Inc Electrostatic charge image developing toner
JPH02110475A (en) * 1988-10-20 1990-04-23 Konica Corp Developer for electrophotography
JPH03251853A (en) * 1989-12-29 1991-11-11 Mita Ind Co Ltd Toner and its production
JPH049862A (en) * 1990-04-27 1992-01-14 Canon Inc Full-color image forming method

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6120053A (en) * 1984-07-06 1986-01-28 Minolta Camera Co Ltd Toner for developing electrostatic latent image
JPS6217751A (en) * 1985-07-16 1987-01-26 Fuji Xerox Co Ltd Developer for electrostatic latent image
JPH01219769A (en) * 1988-02-29 1989-09-01 Canon Inc Electrostatic charge image developing toner
JPH02110475A (en) * 1988-10-20 1990-04-23 Konica Corp Developer for electrophotography
JPH03251853A (en) * 1989-12-29 1991-11-11 Mita Ind Co Ltd Toner and its production
JPH049862A (en) * 1990-04-27 1992-01-14 Canon Inc Full-color image forming method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1026553A1 (en) * 1999-02-03 2000-08-09 Lexmark International, Inc. Toner composition including positive and negative triboelectric charged hydrophobic extra-particulate additives

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