JPH0439669A - Electrostatic charge image developing toner - Google Patents

Electrostatic charge image developing toner

Info

Publication number
JPH0439669A
JPH0439669A JP2145285A JP14528590A JPH0439669A JP H0439669 A JPH0439669 A JP H0439669A JP 2145285 A JP2145285 A JP 2145285A JP 14528590 A JP14528590 A JP 14528590A JP H0439669 A JPH0439669 A JP H0439669A
Authority
JP
Japan
Prior art keywords
toner
fine particles
resin
particles
fine powder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2145285A
Other languages
Japanese (ja)
Inventor
Kenji Yamane
健二 山根
Hiroshi Yamazaki
弘 山崎
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.)
Konica Minolta Inc
Original Assignee
Konica Minolta Inc
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 Konica Minolta Inc filed Critical Konica Minolta Inc
Priority to JP2145285A priority Critical patent/JPH0439669A/en
Publication of JPH0439669A publication Critical patent/JPH0439669A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To effectively clean up th surface of a photosensitive body without damaging it and to obtain electrostatic charge image developing toner stabilized in frictional electricity by incorporating inorganic fine powder in resin particulates. CONSTITUTION:Coloring particulates consisting of binder resin and a coloring agent and composite particulates obtained by incorporating inorganic fine powder in resin particulates are incorporated in the toner. In this constitution, the abrasive property of the composite particulates can be appropriately set up and the reduction of insulating property of the composite particulates can be effectively suppressed. Consequently appropriate abrasive property and effective cleaning property can be displayed without damaging the surface of the photosensitive body, electrostatic attraction to coloring particulates can be improved and the uniformity and stability of frictional electrification of toner can be sharply improved.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、電子写真法、静電証録法、静電写真法等に用
いられる静電荷像現像用トナーに関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a toner for developing electrostatic images used in electrophotography, electrostatic recording, electrostatic photography, and the like.

〔従来の技術〕[Conventional technology]

電子写真法の一例においては、光導電性感光体上に、帯
電、露光により静電荷像が形成され、この静電荷像はト
ナーを含む現像剤によって現像されてトナー像が形成さ
れ、次いでこのトナー像が転写材に転写され、定着され
て可視画像が形成される。一方、転写材に転写されずに
感光体上に残留したトナーは、ブレード等のクリーニン
グ手段によりクリーニングされる。
In an example of electrophotography, an electrostatic charge image is formed on a photoconductive photoreceptor by charging and exposure, and this electrostatic charge image is developed with a developer containing toner to form a toner image. The image is transferred to a transfer material and fused to form a visible image. On the other hand, toner remaining on the photoreceptor without being transferred to the transfer material is cleaned by a cleaning means such as a blade.

このような電子写真法に適用されるトナーにおいては、
高いクリーニング性、適度な研磨性が必要とされる。す
なわち、トナーのクリーニング性が低い場合はクリーニ
ングされないで感光体の表面に残留したトナーによって
画像汚れが発生する。
In toners applied to such electrophotographic methods,
High cleaning properties and appropriate polishing properties are required. That is, if the toner has low cleaning properties, image stains occur due to toner remaining on the surface of the photoreceptor without being cleaned.

また、トナーの研磨性が高すぎる場合は感光体の表面に
損傷が発生し、その損傷部にトナー物質が埋め込まれて
次の画像の形成時に画像に点状の汚れとなって現れる。
Furthermore, if the abrasiveness of the toner is too high, damage will occur on the surface of the photoreceptor, toner material will be embedded in the damaged area and appear as dots on the image when the next image is formed.

一方、トナーの研磨性が低すぎる場合は感光体の表面に
トナー物質が徐々に付着堆積していき感光体の電気的特
性が低下する。
On the other hand, if the abrasiveness of the toner is too low, toner substances will gradually adhere and accumulate on the surface of the photoreceptor, resulting in a decrease in the electrical characteristics of the photoreceptor.

しかるに、トナーのクリーニング性および研磨性に関す
る技術としては、従来、以下に掲げるものが提案されて
いる。
However, as techniques related to toner cleaning and polishing properties, the following have been proposed so far.

■ トナー粉末に、当該トナー粉末より小径のアクリル
系重合体微粉末を添加混合する技術(特開昭60−18
6851号公報)。
■ Technology of adding and mixing acrylic polymer fine powder with a smaller diameter than the toner powder (Japanese Patent Laid-Open No. 60-18
6851).

■ トナー粒子に、樹脂粒子の表面がニッケル等の金属
により処理された球形微粒子を添加混合する技術(特開
昭63−11956号公報)。
(2) A technique of adding and mixing spherical fine particles whose surfaces are treated with a metal such as nickel to toner particles (Japanese Patent Application Laid-open No. 11956/1983).

■ 結着樹脂粉体に、これより小径の樹脂微粉体の表面
に無機微粉体が機械的な衝撃力によって固着されてなる
複合微粉体を添加混合する技術(特開昭64−9114
3号公報)。
■ Technology of adding and mixing composite fine powder, which is made by fine inorganic powder fixed to the surface of fine resin powder with a smaller diameter by mechanical impact force, to the binder resin powder (Japanese Patent Laid-Open No. 64-9114
Publication No. 3).

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかし、上記■の技術では、アクリル系重合体微粉末の
硬度が低いために十分な研磨性が発揮されない。従って
、画像の形成を繰り返すに従って感光体の表面がトナー
物質によりフィルミングされるようになって感光体の電
気的特性が早期に低下する問題がある。
However, in the technique (2) above, sufficient abrasiveness cannot be exhibited because the hardness of the acrylic polymer fine powder is low. Therefore, as images are repeatedly formed, the surface of the photoreceptor becomes filmed with toner material, which causes a problem in that the electrical characteristics of the photoreceptor deteriorate early.

一方、上記■のトナーにおいて、トナー物質による感光
体のフィルミングを防止するためにクリーニングブレー
ドの感光体の表面に対する押圧力を大きくする場合は、
当該ブレードの変形が大きくなってその耐久性が著しく
低下する。
On the other hand, in the case of the above toner (■), when increasing the pressing force of the cleaning blade against the surface of the photoreceptor in order to prevent filming of the photoreceptor by the toner substance,
The deformation of the blade becomes large and its durability is significantly reduced.

また、上記■のトナーが一成分トナーである場合は、ト
ナーに磁性体が含有されるためにトナー粉末とアクリル
系重合体微粉末との比重差が大きくなり、トナー粉末に
アクリル系重合体微粉末を添加混合する際に均一な混合
が困難となる。その結果、トナーの摩擦帯電性が不安定
となったり、またアクリル系重合体微粉末がトナー粒子
から容易に飛散して機内を汚染したり、さらには、トナ
ーを現像領域に搬送するための現像スリーブ上にアクリ
ル系重合体微粉末が固着して現像剤の搬送性が悪化する
問題がある。
In addition, if the toner described in (■) above is a one-component toner, the difference in specific gravity between the toner powder and the acrylic polymer fine powder becomes large because the toner contains a magnetic material, and the toner powder contains a fine acrylic polymer powder. Uniform mixing becomes difficult when adding and mixing powder. As a result, the triboelectric charging properties of the toner become unstable, the acrylic polymer fine powder easily scatters from the toner particles and contaminates the inside of the machine, and furthermore, the developing area for transporting the toner to the developing area becomes unstable. There is a problem in that fine acrylic polymer powder adheres to the sleeve, resulting in poor developer conveyance.

上記■の技術では、球形微粒子を構成する樹脂粒子の表
面を処理する処理材料が−”/ケル等の金属であってそ
の体積固有抵抗が10−8〜105 Ω・cm程度の低
抵抗であるため、トナー粒子に球形微粒子を添加混合す
る際に球形微粒子がトナー粒子に静電的に付着しにくく
なり、その結果、トナーの摩擦帯電性が不安定となった
り、また、現像スリーブの表面に球形微粒子が固着して
現像剤の搬送性が悪化する問題がある。
In the technique (2) above, the processing material used to treat the surface of the resin particles constituting the spherical fine particles is a metal such as -''/Kel, which has a low volume resistivity of about 10-8 to 105 Ωcm. Therefore, when spherical fine particles are added and mixed with toner particles, it becomes difficult for the spherical fine particles to electrostatically adhere to the toner particles, and as a result, the triboelectric charging properties of the toner become unstable, and the surface of the developing sleeve There is a problem in that the spherical fine particles stick to each other and the transportability of the developer deteriorates.

上記■の技術では、無機微粉体が樹脂微粉体の表面にの
み固着されているため、複合微粉体の表面硬度が高くな
りすぎ、また複合微粉体の表面の凹凸が激しいために、
研磨性が過剰となって感光体の表面に損傷が発生する。
In the technique (■) above, the inorganic fine powder is fixed only to the surface of the resin fine powder, so the surface hardness of the composite fine powder becomes too high, and the surface of the composite fine powder is extremely uneven.
Excessive abrasiveness causes damage to the surface of the photoreceptor.

そして当該損傷部にトナー物質が埋め込まれてクリーニ
ングされないようになり、次の画像の形成においては画
像に黒ポチが発生する問題がある。
Then, the toner substance becomes embedded in the damaged area and cannot be cleaned, so that there is a problem that black spots occur in the image when the next image is formed.

本発明は以上の事情に基づいてなされたものであって、
その目的は、感光体の表面を損傷することなく良好にク
リーニングされ、しかも摩擦帯電性が安定した静電荷像
現像用トナーを提供することにある。
The present invention was made based on the above circumstances, and
The purpose is to provide a toner for developing electrostatic images that can be cleaned well without damaging the surface of a photoreceptor and has stable triboelectric charging properties.

〔課題を解決するための手段〕[Means to solve the problem]

以上の目的を達成するため、本発明者らが鋭意研究を重
ねた結果、樹脂微粒子の表面ではなくて樹脂微粒子中に
特に無機微粉を含有させることにより、得られる複合微
粒子の硬度が適度なものとなり、しかも複合微粒子の表
面の絶縁性が十分に高く維持され、その結果、研磨性が
適度となって感光体の表面を損傷することなく良好にク
リーニングを行うことができ、またトナーの摩擦帯電性
が長期間にわたり安定することを見出して、本発明を完
成するに至ったものである。
In order to achieve the above object, the present inventors have conducted extensive research and found that by incorporating inorganic fine powder into the resin fine particles instead of on the surface of the resin fine particles, the resulting composite fine particles have an appropriate hardness. In addition, the surface insulation of the composite fine particles is maintained at a sufficiently high level, and as a result, the abrasiveness is moderate, allowing for good cleaning without damaging the surface of the photoreceptor, and also reducing frictional electrification of the toner. The present invention was completed based on the discovery that the properties are stable over a long period of time.

そこで、本発明の静電荷像現像用トナーにおいては、少
なくともバインダー樹脂と着色剤とからなる着色粒子と
、樹脂微粒子中に無m′R1粉が含有されてなる複合微
粒子とを含有してなることを特徴とする。
Therefore, the toner for developing electrostatic images of the present invention contains at least colored particles made of a binder resin and a colorant, and composite fine particles made of resin fine particles containing m'R1-free powder. It is characterized by

〔作用〕[Effect]

本発明では、複合微粒子において、樹脂微粒子の表面で
はなくて樹脂微粒子の内部に無機微粉を存在させるとい
う特別の構成を採用することによって、複合微粒子の研
磨性を適度なものとし、かつ複合微粒子の絶縁性の低下
を有効に防止することができたものである。
In the present invention, the composite fine particles have a special structure in which inorganic fine powder is present inside the resin fine particles instead of on the surface of the resin fine particles, so that the abrasiveness of the composite fine particles is made appropriate, and the composite fine particles are This effectively prevented the deterioration of insulation properties.

詳しく説明すると、複合微粒子を構成する樹脂微粒子の
内部に無機微粉が含有されているので、単に表面のみに
無機微粉が存在する場合に比して、複合微粒子の硬度が
過大または過小とならず好適なものとなり、その結果、
研磨性が適度となって感光体の表面に付着したトナー物
質を良好に研磨して当該感光体の表面特性を長期間にわ
たり安定に維持することができる。
To explain in detail, since inorganic fine powder is contained inside the resin fine particles constituting the composite fine particles, it is preferable that the hardness of the composite fine particles does not become too large or small compared to the case where inorganic fine powder is simply present only on the surface. As a result,
The abrasiveness becomes appropriate, so that the toner material adhering to the surface of the photoreceptor can be satisfactorily polished, and the surface characteristics of the photoreceptor can be stably maintained over a long period of time.

そして、無機微粉が低抵抗の材料である場合にも、当該
無機微粉が樹脂微粒子の内部に含有されるので、樹脂微
粒子の表面における絶縁性は十分に高く維持される。従
って、着色粒子に対して複合微粒子を添加混合する際に
当該複合微粒子が静電的に十分に着色粒子に付着するよ
うになり、複合微粒子の着色粒子からの遊離、飛散等が
生じない。
Even when the inorganic fine powder is a low-resistance material, the inorganic fine powder is contained inside the resin fine particles, so that the insulation on the surface of the resin fine particles is maintained at a sufficiently high level. Therefore, when the composite fine particles are added to and mixed with the colored particles, the composite fine particles are sufficiently electrostatically attached to the colored particles, and the composite fine particles are not separated from the colored particles or scattered.

また、−成分現像剤用のトナーである場合は、着色粒子
の内部に磁性体が含有されるが、複合微粒子の内部にも
無機微粉が含有され、その含有量は適度な研磨性を得る
ために比較的多量とすることもできるので、着色粒子と
複合微粒子の比重の差が小さくなり、着色粒子に対して
複合微粒子を添加混合する際に、両者が十分に均一に混
合されるようになる。その結果、複合微粒子の着色粒子
に対する付着性が向上し、トナーの摩擦帯電性の均一性
および安定性が格段に向上する。従って、複合微粒子が
遊離して現像スリーブに固着されたり、飛散して機内を
汚染するおそれがなく、トナーを現像領域に安定して搬
送することが可能となる。
In addition, in the case of a toner for a -component developer, a magnetic substance is contained inside the colored particles, but inorganic fine powder is also contained inside the composite fine particles, and the content is adjusted to obtain appropriate abrasiveness. Since it can be used in a relatively large amount, the difference in specific gravity between the colored particles and the composite fine particles becomes small, and when the composite fine particles are added to the colored particles and mixed, they are mixed sufficiently uniformly. . As a result, the adhesion of the composite fine particles to the colored particles is improved, and the uniformity and stability of the triboelectric charging properties of the toner are significantly improved. Therefore, there is no fear that the composite fine particles will become loose and stick to the developing sleeve or scatter and contaminate the inside of the machine, and it is possible to stably transport the toner to the developing area.

従って、本発明のトナーによれば、研磨性およびクリー
ニング性が良好であって感光体の表面を常に良好な状態
に維持することができ、しかも摩擦帯電性が均一でかつ
長期間安定したものとなるため、カブリ、黒ポチ等の画
像不良を伴わずに、高濃度で良好な画像を多数回にわた
り安定に形成することができる。
Therefore, according to the toner of the present invention, the surface of the photoreceptor can always be maintained in a good condition with good polishing properties and cleaning properties, and the triboelectric charging properties are uniform and stable for a long period of time. Therefore, high-density, good images can be stably formed many times without image defects such as fog or black spots.

〔発明の具体的構成〕[Specific structure of the invention]

以下、本発明の構成を具体的に説明する。 Hereinafter, the configuration of the present invention will be specifically explained.

本発明のトナーを構成する複合微粒子は、樹脂微粒子中
に無機微粉が含有されてなるものである。
The composite fine particles constituting the toner of the present invention are composed of resin fine particles containing inorganic fine powder.

複合微粒子の平均粒径は、0.1〜7.0μmの範囲が
好ましく、特に0.2〜5.0 μmの範囲が好ましい
。複合微粒子の平均粒径が斯かる範囲にあれば、トナー
の摩擦帯電性の安定性右よび均一性がさらに向上し、ク
リーニング性がさらに向上する。
The average particle size of the composite fine particles is preferably in the range of 0.1 to 7.0 μm, particularly preferably in the range of 0.2 to 5.0 μm. If the average particle size of the composite fine particles is within this range, the stability and uniformity of the triboelectric charging properties of the toner will further improve, and the cleaning performance will further improve.

しかし、複合微粒子の平均粒径が大きすぎる場合は、ト
ナーの摩擦帯電性が悪化して画像濃度の低下を招来しや
すい。一方、複合微粒子の平均粒径が小さすぎる場合は
、クリーニング性が不十分となりやすい。
However, if the average particle size of the composite fine particles is too large, the triboelectric charging properties of the toner deteriorate, which tends to cause a decrease in image density. On the other hand, if the average particle size of the composite fine particles is too small, cleaning properties tend to be insufficient.

ここで、複合微粒子の平均粒径は、SYMPATEC社
製のレーザ回折式粒度分布測定装置「HELO3−CO
MPETITION/3Jにより測定される体積基準の
平均粒径をいう。
Here, the average particle size of the composite fine particles is determined using a laser diffraction particle size distribution analyzer "HELO3-CO" manufactured by SYMPATEC.
It refers to the volume-based average particle size measured by MPETITION/3J.

複合微粒子のトナーにおける含有割合は、0.01〜5
.f)重量%の範囲が好ましく、特に0.1〜3.0重
量%の範囲が好ましい。含有割合が斯かる範囲にあれば
、複合微粒子による上記作用が十分に発揮される。しか
し、複合微粒子の含有割合が大きすぎるときはトナーの
摩擦帯電性が不十分となって画像濃度の低下を招来しや
すい。一方、複合微粒子の含有割合が小さすぎるときは
トナーのクリーニング性が不十分となりやすい。
The content ratio of the composite fine particles in the toner is 0.01 to 5.
.. f) A range of % by weight is preferred, particularly a range of 0.1 to 3.0% by weight. If the content ratio is within this range, the above-mentioned effects of the composite fine particles will be fully exhibited. However, when the content of the composite fine particles is too large, the triboelectric charging properties of the toner become insufficient, which tends to cause a decrease in image density. On the other hand, when the content of the composite fine particles is too small, the cleaning properties of the toner tend to be insufficient.

複合微粒子を構成する樹脂材料としては、アクリル系重
合体く例えば特開昭60−186851号公報に記載の
アクリル系重合体)、アクリル・スチレン系共重合体(
例えば特開昭60−186852号公報に記載のアクリ
ル・スチレン系共重合体)、含窒素付加重合性単量体の
重合体もしくは共重合体(例えば特開昭60−1868
53号公報に記載の含窒素付加重合性単量体の重合体も
しくは共重合体)、付加重合性カルボン酸の重合体もし
くは共重合体(例えば特開昭60−186868号公報
に記載の付加重合性カルボン酸の重合体もしくは共重合
体)、フッ素樹脂(例えば特願昭62−67997号明
細書に記載のフッ素樹脂)、シリコーン樹脂(例えば特
願昭62−131258号明細書に記載のンリコーン樹
脂)、ポリオレフィン樹脂(例えば特開昭52−891
66号公報に記載のポリオレフィン樹脂)等を用いるこ
とができる。
Examples of the resin material constituting the composite fine particles include acrylic polymers (for example, the acrylic polymer described in JP-A-60-186851), acrylic-styrene copolymers (
For example, acrylic-styrenic copolymers described in JP-A-60-186852), polymers or copolymers of nitrogen-containing addition-polymerizable monomers (e.g., JP-A-60-1868)
Polymers or copolymers of nitrogen-containing addition-polymerizable monomers described in Japanese Patent Publication No. 53), polymers or copolymers of addition-polymerizable carboxylic acids (for example, addition polymerization described in JP-A-60-186868) polymers or copolymers of polycarboxylic acids), fluororesins (e.g., fluororesins described in Japanese Patent Application No. 62-67997), silicone resins (e.g., silicone resins described in Japanese Patent Application No. 131258/1980) ), polyolefin resins (for example, JP-A-52-891
The polyolefin resin described in Japanese Patent Application No. 66), etc. can be used.

複合微粒子を構成する無機微粉としては、シリカ、アル
ミナ、チタニア、チタン酸バリウム、チタン酸アルミニ
ウム、チタン酸マグネシウム、チタン酸カルシウム、チ
タン酸ストロンチウム、酸化亜鉛、酸化クロム、酸化セ
リウム、三酸化アンチモン、酸化ジルコニウム、酸化タ
ングステン、酸化銅、酸化スズ、酸化テルノペ酸化マン
ガン、酸化ホウ素、炭化ケイ素、炭化チタン、炭化ホウ
素、窒化ケイ素、窒化チタン、窒化ホウ素等の無機化合
物、銅、アルミニウム、亜鉛等の金属を用いることがで
きる。
The inorganic fine powders that make up the composite fine particles include silica, alumina, titania, barium titanate, aluminum titanate, magnesium titanate, calcium titanate, strontium titanate, zinc oxide, chromium oxide, cerium oxide, antimony trioxide, and oxide. Inorganic compounds such as zirconium, tungsten oxide, copper oxide, tin oxide, manganese oxide, boron oxide, silicon carbide, titanium carbide, boron carbide, silicon nitride, titanium nitride, boron nitride, and metals such as copper, aluminum, and zinc. Can be used.

無機微粉の一次粒子径は、0.005〜5μmの範囲が
好ましく、特に0.01〜2μmの範囲が好ましい。無
機微粉の一次粒子径が斯かる範囲にあれば、樹脂微粒子
中への無機微粉の分散性を高めることができる。ただし
、無機微粉の一次粒子径が大きすぎるときは複合微粒子
の製造が困難となりやすい。一方、無機微粉の一次粒子
径が小さすぎるときはやはり複合微粒子の製造が困難と
なりやすいほか、トナーのクリーニング性が低下しやす
い。
The primary particle diameter of the inorganic fine powder is preferably in the range of 0.005 to 5 μm, particularly preferably in the range of 0.01 to 2 μm. If the primary particle size of the inorganic fine powder is within this range, the dispersibility of the inorganic fine powder into the resin fine particles can be improved. However, when the primary particle size of the inorganic fine powder is too large, it tends to be difficult to produce composite fine particles. On the other hand, when the primary particle size of the inorganic fine powder is too small, it tends to be difficult to produce composite fine particles, and the cleaning properties of the toner tend to deteriorate.

無機微粉の複合微粒子における含有割合は、10〜95
重量%の範囲が好ましく、特に20〜80重量%の範囲
が好ましい。無機微粉の含有割合が斯かる範囲にあれば
、複合微粒子の研磨性および絶縁性がさらに好適な範囲
となる。ただし、無機微粉の含有割合が大きすぎるとき
は複合微粒子の製造が困難となり、無機微粉を十分に内
包することが難しくなる。一方、無機微粉の含有割合が
小さすぎるときはトナーのクリーニング性が低下しやす
い。
The content ratio of the inorganic fine powder in the composite fine particles is 10 to 95
A range of % by weight is preferred, particularly a range of 20 to 80% by weight. If the content of the inorganic fine powder is within this range, the abrasiveness and insulation properties of the composite fine particles will be in a more suitable range. However, if the content of the inorganic fine powder is too large, it becomes difficult to manufacture composite fine particles, and it becomes difficult to sufficiently encapsulate the inorganic fine powder. On the other hand, when the content of the inorganic fine powder is too small, the cleaning properties of the toner tend to deteriorate.

本発明のトナーを構成する複合微粒子は、例えば次のよ
うな方法によって製造することができる。
The composite fine particles constituting the toner of the present invention can be produced, for example, by the following method.

(1)無機微粉の存在下で、樹脂微粒子を構成する樹脂
の七ツマ−を重合する方法。
(1) A method of polymerizing the seven polymers of resin constituting fine resin particles in the presence of inorganic fine powder.

この方法は、樹脂微粒子を構成する樹脂によって無機微
粉をカプセル化する方法であり、樹脂と無機微粉との親
和性を高めることが重要であり、具体的には、以下の方
法を適用することができる。
This method is a method in which inorganic fine powder is encapsulated by resin constituting resin fine particles, and it is important to increase the affinity between the resin and inorganic fine powder. Specifically, the following method can be applied. can.

(a)  無機微粉の表面をあらかじめ有機高分子や界
面活性剤等により吸着処理または反応処理を行って樹脂
微粒子を構成する樹脂のモノマーに対し親和性の表面を
形成し、この無機微粉を芯として樹脂のモノマーを重合
して当該無機微粉を樹脂によりカプセル化する方法。
(a) The surface of the inorganic fine powder is previously subjected to adsorption treatment or reaction treatment with organic polymers, surfactants, etc. to form a surface that has an affinity for the resin monomers that make up the resin fine particles, and this inorganic fine powder is used as a core. A method of polymerizing a resin monomer and encapsulating the inorganic fine powder with the resin.

ら)無機微粉の存在下において、樹脂微粒子を構成する
樹脂のモノマーを重合して、当該無機微粉の表面電荷に
対し逆の極性のイオン性基末端を有する樹脂を形成し、
両電荷の静電引力により無機微粉を樹脂によりカプセル
化する方法。
et al.) in the presence of an inorganic fine powder, polymerizing a resin monomer constituting the resin fine particles to form a resin having an ionic group terminal with a polarity opposite to the surface charge of the inorganic fine powder,
A method of encapsulating inorganic fine powder with resin using the electrostatic attraction of both charges.

例えば乳化剤フリーの系で調製される樹脂微粒子の末端
には、重合に使用された触媒の分解切片の電荷によって
電荷が付与されるのでこの方法を適用が可能である。
For example, this method can be applied to the ends of fine resin particles prepared in an emulsifier-free system because they are charged by the charges of decomposed fragments of the catalyst used in polymerization.

(2)無機微粉を前処理後、複合微粒子を生成させる方
法。
(2) A method in which composite fine particles are generated after pretreatment of inorganic fine powder.

具体的には、熱可塑性樹脂に無機微粉を混合して両者を
混練し、これを粉砕して粉末を製造し、この粉末を溶剤
に溶解した後、これを熱可塑性樹脂の賞溶媒と混合して
複合微粒子を晶析する方法、あるいは溶解した後冷却す
ることによって複合微粒子を析出させる方法等がある。
Specifically, a thermoplastic resin is mixed with an inorganic fine powder, the two are kneaded, this is pulverized to produce a powder, this powder is dissolved in a solvent, and then this is mixed with a prize solvent for the thermoplastic resin. There are methods such as crystallizing composite fine particles by melting, or precipitating composite fine particles by cooling after melting.

(3)乳化重合法を利用した方法。(3) A method using emulsion polymerization.

磁性粉と樹脂微粒子を構成する樹脂モノマーとを混合し
、分散液を作製する。次いで、分散液を界面活性剤を含
有する溶液中に乳化させ乳化重合することによって磁性
粉を含有した微粒子を得る。
A dispersion liquid is prepared by mixing the magnetic powder and a resin monomer constituting the resin fine particles. Next, the dispersion is emulsified in a solution containing a surfactant and subjected to emulsion polymerization to obtain fine particles containing magnetic powder.

本発明のトナーを構成する着色粒子は1.(イングー樹
脂と着色剤とを必須成分として含有してなる粒子であり
、必要に応じて荷電制御剤、定着性改良剤、磁性体等の
内部添加剤が含有されていてもよい。
The colored particles constituting the toner of the present invention are 1. (Particles containing an Ingu resin and a colorant as essential components, and may contain internal additives such as a charge control agent, a fixing property improver, and a magnetic material as necessary.

バインダー樹脂としては、特に限定されず、トナーのバ
インダー樹脂として従来から用いられている樹脂を用い
ることができる。具体的には、スチレン樹脂、アクリル
樹脂、スチレン・アクリル共重合体樹脂、ポリエステル
樹脂、エポキシ樹脂、ポリウレタン樹脂、ポリイミド樹
脂、セルロース樹脂、ポリエーテル樹脂等を挙げること
ができる。
The binder resin is not particularly limited, and resins conventionally used as binder resins for toners can be used. Specifically, styrene resin, acrylic resin, styrene/acrylic copolymer resin, polyester resin, epoxy resin, polyurethane resin, polyimide resin, cellulose resin, polyether resin, etc. can be mentioned.

着色剤としては、カーボンブラック、ニグロシン染料、
アニリンブルー、カルコオイルブルークロムイエロー、
ウルトラマリンブルー、デュポンオイルレッド、キノリ
ンイエロー、メチレンブルークロライド、フタロシアニ
ンブルー マラカイトグリーンオフサレート、ランプブ
ラック、ローズベンガノペ磁性体、これらの混合物等を
用いることかできる。
Colorants include carbon black, nigrosine dye,
Aniline blue, Calco oil blue chrome yellow,
Ultramarine blue, DuPont oil red, quinoline yellow, methylene blue chloride, phthalocyanine blue, malachite green offsalate, lamp black, rose benganope magnetic material, mixtures thereof, and the like can be used.

荷電制御剤としては、例えばニグロシン系染料、含金属
アゾ染料、金属錯体等を用いる二とができる。
As the charge control agent, for example, nigrosine dyes, metal-containing azo dyes, metal complexes, etc. can be used.

定着性改良剤としては、例えば低分子量ポリプロピレン
等のポリオレフィン等を用いることができる。
As the fixing property improving agent, for example, polyolefin such as low molecular weight polypropylene can be used.

磁性体は、主として磁性トナーを得る場合に用いられる
内部添加剤であって、各種のフェライト、マグネタイト
、ヘマタイト等の鉄、亜鉛、コバルト、ニッケル、マン
ガン等の合金もしくは化合物等を用いることができる。
The magnetic substance is an internal additive mainly used when obtaining a magnetic toner, and alloys or compounds of iron such as various ferrites, magnetites, hematites, zinc, cobalt, nickel, manganese, etc. can be used.

磁性体の平均粒径は1μm以下が好ましく、特に0.5
μm以下が好ましい。磁性体の配合量は、着色粒子全体
の20〜70重量%の範囲である。
The average particle size of the magnetic material is preferably 1 μm or less, particularly 0.5 μm or less.
It is preferably less than μm. The blending amount of the magnetic material is in the range of 20 to 70% by weight of the entire colored particles.

着色粒子を製造する方法としては、粉砕造粒法、重合造
粒法等を適用することができる。
As a method for producing colored particles, a pulverization granulation method, a polymerization granulation method, etc. can be applied.

粉砕造粒法は、バインダー樹脂と、着色剤と、必要に応
じて用いられるその他のトナー成分とを混合し、溶融混
練し、粉砕し、分級して、所定の平均粒径(1〜30μ
m程度)の着色粒子を製造する方法である。
In the pulverization granulation method, a binder resin, a colorant, and other toner components used as necessary are mixed, melt-kneaded, pulverized, and classified to give a predetermined average particle size (1 to 30 μm).
This is a method for producing colored particles of about 1.0 m).

重合造粒法は、バインダー樹脂を構成するモノマー中に
、着色剤、必要に応じて用いられるその他のトナー成分
を存在させて、懸濁重合法、乳化重合法等により重合反
応を行って、所定の平均粒径(1〜30μm程度)の着
色粒子を製造する方法である。
In the polymerization granulation method, a colorant and other toner components used as necessary are present in the monomers constituting the binder resin, and a polymerization reaction is carried out by suspension polymerization, emulsion polymerization, etc. This is a method for producing colored particles having an average particle size (approximately 1 to 30 μm).

本発明のトナーは、着色粒子と、複合微粒子とを含有し
てなるものであり、具体的には、着色粒子と複合微粒子
とを混合撹拌して、着色粒子の表面に複合微粒子を静電
的に付着させてトナーを構成する。
The toner of the present invention contains colored particles and composite fine particles. Specifically, the colored particles and the composite fine particles are mixed and stirred, and the composite fine particles are electrostatically applied to the surface of the colored particles. to form a toner.

本発明においては、以上のようにして得られるトナーに
、さらに無機微粒子等を外部から添加混合してトナーを
構成してもよい。斯かる無機微粒子としては、例えばシ
リカ、アルミナ、チタニア等の微粒子が好ましく、特に
疎水性シリカ微粒子が好ましい。
In the present invention, the toner may be constituted by further adding and mixing inorganic fine particles and the like from the outside to the toner obtained as described above. As such inorganic fine particles, for example, fine particles of silica, alumina, titania, etc. are preferable, and hydrophobic silica fine particles are particularly preferable.

本発明のトナーは、キャリアと混合されて二成分現像剤
を構成する二成分トナーであってもよく、またキャリア
を用いずにトナーのみからなる一成分現像剤を構成する
一成分トナーであってもよい。
The toner of the present invention may be a two-component toner that is mixed with a carrier to form a two-component developer, or a one-component toner that is composed of only toner without using a carrier. Good too.

〔実施例〕〔Example〕

以下、本発明の実施例を比較例と共に説明するが、本発
明の実施のt=Wはこれらに限定されるものではない。
Examples of the present invention will be described below along with comparative examples, but t=W in the implementation of the present invention is not limited to these examples.

なお、以下において「部」は「重量部」を表す。In addition, in the following, "part" represents "part by weight".

〈複合微粒子の製造〉 (1)複合微粒子1 一次粒子の平均径が0.2μmの不定形の炭化ケイ素(
無機微粉) 150 gと、メチルトリメトキシシラン
6gとをトルエン中に加え、撹拌しながら温度100℃
まで加熱し、その温度で約2時間にわたり熱処理し、そ
の後トルエンを留去した。生成物を洗浄し、乾燥して、
表面が改質された無機微粉1を得た。
<Manufacture of composite fine particles> (1) Composite fine particles 1 Amorphous silicon carbide with an average primary particle diameter of 0.2 μm (
150 g of inorganic fine powder) and 6 g of methyltrimethoxysilane were added to toluene, and the temperature was raised to 100°C while stirring.
The mixture was heated at that temperature for about 2 hours, and then the toluene was distilled off. Wash and dry the product,
Inorganic fine powder 1 with a modified surface was obtained.

この無機微粉1の10gと、スチレン(ビニルモノマー
)50gと、AIBN(アゾビスイソブチロニトリル:
重合開始剤)1gと、アエロジル○T(スルホコハク酸
ジー2−エチルヘキシルエステルナトリウム塩:界面活
性剤)の適量とを用い、エタノール中で窒素気流下70
℃で約2時間にわたり反応を行って、平均粒径が0.3
μmの複合微粒子1を製造した。
10 g of this inorganic fine powder 1, 50 g of styrene (vinyl monomer), and AIBN (azobisisobutyronitrile:
Using 1 g of polymerization initiator) and an appropriate amount of Aerosil ○T (sulfosuccinic acid di-2-ethylhexyl ester sodium salt: surfactant), the mixture was heated in ethanol for 70 minutes under a nitrogen stream.
The reaction was carried out at ℃ for about 2 hours, and the average particle size was 0.3.
Composite fine particles 1 of μm size were manufactured.

この複合微粒子1の表面を電子顕微鏡により観察したと
ころ、その表面には炭化ケイ素粒子はほとんど観察され
ず、樹脂微粒子の内部に含有されていることが確認でき
た。
When the surface of this composite fine particle 1 was observed using an electron microscope, it was confirmed that almost no silicon carbide particles were observed on the surface, and that silicon carbide particles were contained inside the resin fine particles.

(2)複合微粒子2 複合微粒子1の製造において、無機微粉を一次粒子の平
均径が0.4μmの不定形の酸化チタン150gに変更
したほかは同様にして表面が改質された無機微粉2を得
た。
(2) Composite fine particles 2 In the production of composite fine particles 1, inorganic fine particles 2 were prepared in the same manner, except that 150 g of amorphous titanium oxide with an average primary particle diameter of 0.4 μm was used as the inorganic fine powder. Obtained.

次いで、無機微粉1を上記無機微粉2の10gに変更し
、スチレンをメチルメタクリレート50gに変更したほ
かは複合微粒子1と同様にして平均粒径が0.5μmの
複合微粒子2を製造した。
Next, Composite Fine Particles 2 having an average particle diameter of 0.5 μm were produced in the same manner as Composite Fine Particles 1 except that Inorganic Fine Powder 1 was changed to 10 g of the above-mentioned Inorganic Fine Powder 2 and styrene was changed to 50 g of methyl methacrylate.

この複合微粒子2の表面を電子顕微鏡により観察したと
ころ、その表面には酸化チタン粒子ははとんど観察され
ず、樹脂微粒子の内部に含有されていることが確認でき
た。
When the surface of the composite fine particles 2 was observed using an electron microscope, it was confirmed that titanium oxide particles were hardly observed on the surface and were contained inside the resin fine particles.

(3)複合微粒子3 複合微粒子1の製造において、無機微粉を一次粒子の平
均径が0.8μmの不定形の酸化アルミニウム150g
に変更したほかは同様にして表面が改質された無機微粉
3を得た。
(3) Composite fine particles 3 In the production of composite fine particles 1, 150 g of amorphous aluminum oxide with an average primary particle diameter of 0.8 μm was added to the inorganic fine powder.
Surface-modified inorganic fine powder 3 was obtained in the same manner except that the method was changed to .

次いで、無機微粉1を上記無機微粉3の10gに変更し
たほかは複合微粒子1と同様にして平均粒径が1.0μ
mの複合微粒子3を製造した。
Next, inorganic fine powder 1 was changed to 10 g of the above-mentioned inorganic fine powder 3, but in the same manner as composite fine particles 1, the average particle size was 1.0 μm.
Composite fine particles 3 of m were manufactured.

この複合微粒子3の表面を電子顕微鏡により観察したと
ころ、その表面には酸化アルミニウム粒子はほとんど観
察されず、樹脂微粒子の内部に含有されていることが確
認できた。
When the surface of the composite fine particles 3 was observed using an electron microscope, it was confirmed that almost no aluminum oxide particles were observed on the surface, and that they were contained inside the resin fine particles.

〈着色粒子の製造〉 (1)着色粒子1 スチレン・アクリル共重合体樹脂   60部(S t
 : BA=85 :15) マグネタイト             45部ニグロ
シン系染′#+(荷電制御剤)    2部低分子量ポ
リプロピレン        3部(ただし、3tはス
チレン、BAはブチルアクリレートを表す。) 以上の材料を混合した後、練肉、粉砕、分級して、平均
粒径が11.0μmの着色粒子1を得た。
<Manufacture of colored particles> (1) Colored particles 1 Styrene-acrylic copolymer resin 60 parts (S t
: BA=85 :15) Magnetite 45 parts Nigrosine dye'#+ (charge control agent) 2 parts Low molecular weight polypropylene 3 parts (3t represents styrene and BA represents butyl acrylate) After mixing the above materials , kneaded, crushed and classified to obtain colored particles 1 having an average particle size of 11.0 μm.

(2)着色粒子2 ポリエステル樹脂          100部カーボ
ンブラック           4部低分子量ポリプ
ロピレン        3部以上の材料を混合し、練
肉、粉砕、分級して、平均粒径が12.0μmの着色粒
子2を得た。
(2) Colored Particles 2 Polyester resin 100 parts Carbon black 4 parts Low molecular weight polypropylene 3 parts or more of the materials were mixed, ground, crushed, and classified to obtain colored particles 2 with an average particle size of 12.0 μm.

〈実施例1〉 着色粒子1に、無機微粒子rR−812J(疎水性シリ
カ微粒子、−次粒子の平均径3nm、  日本アエロジ
ル社製)を0.4重量%、複合微粒子1を0.4重量%
となる割合で加え、これらをV型混合機により混合して
本発明のトナーAを得た。
<Example 1> In the colored particles 1, 0.4% by weight of inorganic fine particles rR-812J (hydrophobic silica fine particles, average particle diameter of 3 nm, manufactured by Nippon Aerosil Co., Ltd.) and 0.4% by weight of composite fine particles 1 were added.
These were mixed using a V-type mixer to obtain toner A of the present invention.

〈実施例2〉 着色粒子1に、無機微粒子rR−972J(疎水性シリ
カ微粒子、−次粒子の平均径15nm、  日本アエロ
ジル社製)を0.6重量%、複合微粒子2を0.6重量
%となる割合で加え、これらをV型混合機により混合し
て本発明のトナーBを得た。
<Example 2> In the colored particles 1, 0.6% by weight of inorganic fine particles rR-972J (hydrophobic silica fine particles, average diameter of secondary particles 15 nm, manufactured by Nippon Aerosil Co., Ltd.) and 0.6% by weight of composite fine particles 2 were added. These were mixed using a V-type mixer to obtain toner B of the present invention.

〈実施例3〉 着色粒子1に、無機微粒子rR−972Jを0.4重量
%、複合微粒子3を0.8重量%となる割合で加え、こ
れらをV型混合機により混合して本発明のトナーCを得
た。
<Example 3> 0.4% by weight of inorganic fine particles rR-972J and 0.8% by weight of composite fine particles 3 were added to colored particles 1, and these were mixed in a V-type mixer to form the inventive particle. Toner C was obtained.

く比較例1〉 実施例1において、複合微粒子1を、特開昭64−91
143号公報の実施例に記載された複合微粉体1 (ア
クリル系重合体粒子(100部)の表面上に炭化ケイ素
微粒子(20部)を固着してなる粒子)の0.6重量%
に変更したほかは同様にして比較用のトナーaを得た。
Comparative Example 1> In Example 1, composite fine particles 1 were
0.6% by weight of composite fine powder 1 (particles formed by adhering silicon carbide fine particles (20 parts) on the surface of acrylic polymer particles (100 parts)) described in Examples of Publication No. 143
Toner a for comparison was obtained in the same manner except that the following was changed.

く比較例2〉 実施例2において、複合微粒子2を、平均粒径が0.4
μmのアクリル系重合体粒子の0.6重量%に変更した
ほかは同様にして比較用のトナーbを得た。
Comparative Example 2> In Example 2, composite fine particles 2 were prepared with an average particle size of 0.4.
A comparative toner b was obtained in the same manner except that the amount of acrylic polymer particles of μm was changed to 0.6% by weight.

〈実施例4〉 着色粒子2に、無機微粒子rR−812Jを0.4重量
%、複合微粒子lを0.6重量%となる割合で加え、こ
れらをV型混合機により混合して本発明のトナーDを得
た。
<Example 4> 0.4% by weight of inorganic fine particles rR-812J and 0.6% by weight of composite fine particles 1 were added to colored particles 2, and these were mixed in a V-type mixer to form the inventive particle. Toner D was obtained.

〈実施例5〉 着色粒子2に、無機微粒子rR−972Jを0.6重量
%、複合微粒子2を0.3重量%となる割合で加え、こ
れらをV型混合機により混合して本発明のトナーEを得
た。
<Example 5> 0.6% by weight of inorganic fine particles rR-972J and 0.3% by weight of composite fine particles 2 were added to colored particles 2, and these were mixed using a V-type mixer to form the inventive compound. Toner E was obtained.

く比較例3〉 実施例4において、複合微粒子1を、比較例1で用いた
複合微粉体1の1,0重量%に変更したほかは同様にし
て比較用のトナーCを得た。
Comparative Example 3 A comparative toner C was obtained in the same manner as in Example 4, except that the amount of composite fine particles 1 was changed to 1.0% by weight of the composite fine powder 1 used in Comparative Example 1.

〈比較例4〉 実施例5において、複合微粒子2を、比較例2で用いた
アクリル系重合体粒子の0.8重量%に変更したほかは
同様にして比較用のトナーdを得た。
<Comparative Example 4> Comparative toner d was obtained in the same manner as in Example 5, except that the composite fine particles 2 were changed to 0.8% by weight of the acrylic polymer particles used in Comparative Example 2.

くテスト1〉 本発明のトナーA−Cおよび比較用のトナーabのそれ
ぞれを一成分系現像剤として用いて、有機感光体を搭載
し、現像領域に振動電界を作用させる非接触型現像器を
備えた一成分現像剤用の電子写真複写機の試作機により
、温度20℃、相対湿度55%の環境条件下でコピー画
像を20万回にわたり連続して形成するテストを行い、
クリーニング性、感光体の損傷、画像濃度、搬送性、複
合微粒子の飛散について評価した。結果は後記第1表に
示す。
Test 1> Using each of the toners A-C of the present invention and the comparative toner ab as a one-component developer, a non-contact type developer equipped with an organic photoreceptor and in which an oscillating electric field is applied to the development area was constructed. Using a prototype electrophotographic copying machine equipped with a single-component developer, we conducted a test in which copy images were continuously formed 200,000 times under environmental conditions of a temperature of 20°C and a relative humidity of 55%.
Cleanability, damage to the photoreceptor, image density, transportability, and scattering of composite particles were evaluated. The results are shown in Table 1 below.

〈テスト2〉 本発明のトナーD、  Eおよび比較用のトナーC1d
のそれぞれ3部と、フェライト芯材の表面にスチレン・
アクリル共重合体樹脂(スチレン:メチルメタクリレー
ト=3ニア)を被覆してなるキャリア(平均粒径80μ
m)97部とを混合して、二成分系現像剤を調製した。
<Test 2> Toners D and E of the present invention and toner C1d for comparison
3 parts each, and styrene on the surface of the ferrite core material.
Carrier coated with acrylic copolymer resin (styrene: methyl methacrylate = 3 nia) (average particle size 80 μm)
m) to prepare a two-component developer.

これらの二成分系現像剤を用いて、セレン系感光体を搭
載した電子写真複写機rU −Bix 5000J(コ
ニカ■製)により、温度20℃、相対湿度55%の環境
条件下に右いて、コピー画像を20万枚にわたり連続し
て形成するテストを行い、テスト1と同様にして、クリ
ーニング性、感光体の損傷、画像濃度、複合微粒子の飛
散について評価した。結果は後言己第2表に示す。
Using these two-component developers, copies were made using an electrophotographic copying machine rU-Bix 5000J (manufactured by Konica) equipped with a selenium-based photoreceptor under environmental conditions of a temperature of 20°C and a relative humidity of 55%. A test was conducted in which images were continuously formed on 200,000 sheets, and in the same manner as Test 1, cleaning performance, damage to the photoreceptor, image density, and scattering of composite fine particles were evaluated. The results are shown in Table 2 below.

以上のテスト1および2において、評価方法は次のとお
りである。
In the above Tests 1 and 2, the evaluation method is as follows.

〔クリーニング性〕[Cleanability]

クリーニングブレードによりクリーニングされた直後の
感光体の表面を目視により観察し、当該感光体の表面へ
の付着物の有無により判定した。
The surface of the photoreceptor immediately after being cleaned with a cleaning blade was visually observed, and judgment was made based on the presence or absence of deposits on the surface of the photoreceptor.

評価は、付着物がほとんど認められず良好である場合を
「○」、付着物が若干認められるが実用レベルにある場
合を「△」、付着物が多く認められ実用的には問題のあ
る場合を「×」とした。
The evaluation is "○" if there is almost no deposits observed and the product is in good condition, "△" if some deposits are observed but at a practical level, and "△" if a lot of deposits are observed and there is a problem in practical use. was marked as "x".

〔感光体の損傷〕[Damage to photoreceptor]

感光体の表面を目視により観察し、損傷の有無を調べた
The surface of the photoreceptor was visually observed to check for damage.

〔画@!濃度〕[Picture @! concentration〕

コニカ■製の「サクラデンシトメーター」を用いて、相
対濃度を測定した。評価は、相対濃度が1.25以上の
場合を10−:、1.1以上で1.25未滴の場合を「
△」、11未満の場合を「×」とした。
The relative concentration was measured using a "Sakura Densitometer" manufactured by Konica ■. The evaluation is 10-: when the relative concentration is 1.25 or more, and 10-: when the relative concentration is 1.1 or more and 1.25 drops.
△", and cases where the score was less than 11 were marked "x".

〔搬送性〕[Transportability]

現像スリーブ上を目視により観察し、複合微粒子の固着
がほとんど認袷られず搬送性が良好である場合を「O」
、現像ス・リーブへの固着が認められ、搬送性が不安定
である場合を「×」とした。
Visually observe the surface of the developing sleeve, and if there is almost no adhesion of composite fine particles and the conveyance is good, the rating is "O".
, Cases where adhesion to the developing sleeve was observed and transportability was unstable were rated "x".

〔複合微粒子の飛散コ 現像剤の層厚を規制する部材の裏側を目視により観察し
て複合微粒子の飛散の有無を調べた。
[Scattering of composite fine particles - The back side of the member that regulates the layer thickness of the developer was visually observed to check for the presence or absence of scattering of composite fine particles.

以上のテストの結果、本発明に係る一成分のトナーA−
Cを用いた場合は、クリーニング性、感光体の損傷、画
像濃度、搬送性、複合微粒子の飛散のすべてにおいて優
れていることが明らかである。また、本発明に係る二成
分のトナーD、  Eを用いた場合においても、クリー
ニング性、感光体の損傷、画像濃度、複合微粒子の飛散
のすべてにおいて優れていることが明らかである。
As a result of the above tests, one-component toner A-
It is clear that when C is used, it is excellent in all aspects of cleaning performance, damage to the photoreceptor, image density, transportability, and scattering of composite fine particles. Furthermore, it is clear that even when the two-component toners D and E according to the present invention are used, they are excellent in all aspects of cleaning performance, damage to the photoreceptor, image density, and scattering of composite fine particles.

すなわち、本発明のトナーを用いた場合は、感光体の表
面を常に良好な状態に維持することができ、良好なりリ
ーニング性が発揮される。
That is, when the toner of the present invention is used, the surface of the photoreceptor can always be maintained in a good condition, and good cleaning properties can be exhibited.

さらに、本発明のトナーが一成分の場合は、複合微粒子
の飛散、現像スリーブへの固着が生じないため、搬送性
、摩擦帯電性が長期間にわたり安定したものとなり、ト
ナー飛散および画像不良を伴わずに画像濃度の高い安定
した画像を20万回にわたり形成することができる。
Furthermore, when the toner of the present invention is made of one component, the composite fine particles do not scatter or stick to the developing sleeve, so the transportability and triboelectric charging properties are stable over a long period of time, and there is no problem with toner scattering or image defects. A stable image with high image density can be formed 200,000 times without any problems.

また、本発明のトナーが二成分の場合も、画像濃度の高
い安定した画像をトナー飛散を伴わずに20万回にわた
り形成することができる。
Further, even when the toner of the present invention is two-component, a stable image with high image density can be formed over 200,000 times without toner scattering.

これに対して、比較用の一成分のトナーaを用いた場合
は、当該トナーに含有された複合微粉体の内部には無機
微粉が含有されておらずその表面に炭化ケイ素微粒子が
固着されているにすぎないため、感光体の表面に損傷が
発生しやすく、クリニング性が劣り、画像形成回数が1
0万回で複合微粉体が現像スリーブに固着し、搬送性が
不安定となり、画像濃度の低下を招いた。
On the other hand, when one-component toner a was used for comparison, the composite fine powder contained in the toner did not contain any inorganic fine powder, and silicon carbide fine particles were fixed to its surface. Because the surface of the photoreceptor is easily damaged, cleaning performance is poor, and the number of image formations is reduced to 1.
After 00,000 cycles, the composite fine powder stuck to the developing sleeve, making the conveyance unstable and causing a decrease in image density.

比較用の一成分のトナーbを用いた場合は、当該トナー
に含有されたアクリル系重合体粒子の内部には無機微粉
が含有されておらずしかもその表面にも無機微粉が存在
していないため1、クリーニング性が劣り、画像形成回
数が3万回でアクリル系重合体粒子が現像スリーブに固
着し、搬送性が不安定となり、画像濃度の低下を招いた
When using one-component toner b for comparison, the acrylic polymer particles contained in the toner did not contain any inorganic fine powder inside, and no inorganic fine powder was present on the surface either. 1. Cleanability was poor, and the acrylic polymer particles stuck to the developing sleeve after 30,000 image formations, resulting in unstable conveyance and a decrease in image density.

比較用の二成分のトナーCを用いた場合は、当該トナー
に含有された複合微粉体の内部には無機微粉が含有され
ておらずその表面に炭化ケイ素微粒子が固着されている
にすぎないため、感光体の表面に損傷が発生しやすく、
クリーニング性が劣り、画像形成回数が12万回で画像
濃度の低下を招いた。
When the comparative two-component toner C was used, the composite fine powder contained in the toner contained no inorganic fine powder, but only silicon carbide fine particles were fixed to its surface. , the surface of the photoreceptor is easily damaged;
Cleanability was poor, and image density decreased after 120,000 image formations.

比較用の二成分のトナーdを用いた場合は、当該トナー
に含有されたアクリル系重合体粒子の内部には無機微粉
が含有されておらずしかもその表面にも無機微粉が存在
していないため、クリーニング性が劣り、画像形成回数
が10万回で画像濃度の低下を招いた。
When using the comparative two-component toner d, there was no inorganic fine powder inside the acrylic polymer particles contained in the toner, and no inorganic fine powder was present on the surface. The cleaning properties were poor, and the image density decreased after 100,000 image formations.

〔発明の効果〕〔Effect of the invention〕

以上説明したように、本発明では、樹脂微粒子の内部に
無機微粉を含有させた複合微粒子を用いるため、複合微
粒子の硬度が適度なものとなり、感光体の表面を損傷す
ることなく好適な研磨性および良好なりリーニング性が
発揮される。
As explained above, in the present invention, since composite fine particles containing inorganic fine powder inside the resin fine particles are used, the hardness of the composite fine particles is appropriate, and suitable abrasiveness is achieved without damaging the surface of the photoreceptor. and exhibits good leaning properties.

Claims (1)

【特許請求の範囲】 少なくともバインダー樹脂と着色剤とからなる着色粒子
と、 樹脂微粒子中に無機微粉が含有されてなる複合微粒子と を含有してなることを特徴とする静電荷像現像用トナー
[Scope of Claims] A toner for developing an electrostatic image, comprising colored particles made of at least a binder resin and a colorant, and composite fine particles made of fine resin particles containing inorganic fine powder.
JP2145285A 1990-06-05 1990-06-05 Electrostatic charge image developing toner Pending JPH0439669A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2145285A JPH0439669A (en) 1990-06-05 1990-06-05 Electrostatic charge image developing toner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2145285A JPH0439669A (en) 1990-06-05 1990-06-05 Electrostatic charge image developing toner

Publications (1)

Publication Number Publication Date
JPH0439669A true JPH0439669A (en) 1992-02-10

Family

ID=15381610

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2145285A Pending JPH0439669A (en) 1990-06-05 1990-06-05 Electrostatic charge image developing toner

Country Status (1)

Country Link
JP (1) JPH0439669A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016038459A (en) * 2014-08-07 2016-03-22 キヤノン株式会社 toner
US9568847B2 (en) 2011-10-26 2017-02-14 Cabot Corporation Toner additives comprising composite particles
US9982166B2 (en) 2013-12-20 2018-05-29 Cabot Corporation Metal oxide-polymer composite particles for chemical mechanical planarization

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9568847B2 (en) 2011-10-26 2017-02-14 Cabot Corporation Toner additives comprising composite particles
US10955763B2 (en) 2011-10-26 2021-03-23 Cabot Corporation Toner additives comprising composite particles
US9982166B2 (en) 2013-12-20 2018-05-29 Cabot Corporation Metal oxide-polymer composite particles for chemical mechanical planarization
JP2016038459A (en) * 2014-08-07 2016-03-22 キヤノン株式会社 toner

Similar Documents

Publication Publication Date Title
JP2006267297A (en) Carrier for electrostatic latent image development, developer for electrostatic latent image development, and image forming method
JP2004347654A (en) Electrostatic latent image developer and image forming method
JP2992907B2 (en) Magnetic toner
JP3286849B2 (en) Carrier for electrostatic latent image development
JPH0439669A (en) Electrostatic charge image developing toner
JPH0421862A (en) Electrostatic charge image developing toner
JPH0439668A (en) Electrostatic charge image developing toner
JPH02141762A (en) Developer for reversal development
JP4010214B2 (en) Carrier for electrostatic image developer, electrostatic image developer
JP2004361887A (en) Carrier for electrostatic latent image developer, electrostatic latent image developer and image forming method
JPH0876436A (en) Binary system developer
JPH0876511A (en) Two-component developer
JPH0876474A (en) Binary system developer
JPH0876498A (en) Binary system developer
JPH0876514A (en) Two-component developer
JPH0876482A (en) Binary system developer
JPH0876489A (en) Binary system developer
JPH0439670A (en) Electrostatically charged image developing toner
JPH0876437A (en) Binary system developer
JPH0876499A (en) Binary system developer
JPH0876488A (en) Binary system developer
JPH0876490A (en) Binary system developer
JPH0876414A (en) Binary system developer
JPH0876500A (en) Binary system developer
JPH0876475A (en) Binary system developer