JP2009036814A - Image forming apparatus - Google Patents

Image forming apparatus Download PDF

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JP2009036814A
JP2009036814A JP2007198702A JP2007198702A JP2009036814A JP 2009036814 A JP2009036814 A JP 2009036814A JP 2007198702 A JP2007198702 A JP 2007198702A JP 2007198702 A JP2007198702 A JP 2007198702A JP 2009036814 A JP2009036814 A JP 2009036814A
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image
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carrier liquid
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JP5162997B2 (en
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Naoki Yoshie
直樹 吉江
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Konica Minolta Business Technologies Inc
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an image forming apparatus having high transfer efficiency in transfer of an image on an image carrier onto a recording medium and capable of forming an image having sufficient fixing strength, with respect to an image forming apparatus using a nonvolatile liquid developer. <P>SOLUTION: The image forming apparatus using a liquid developer includes: a developing means for performing development with the liquid developer including a nonvolatile carrier liquid, charged pigment fine particles dispersed in the carrier liquid, and thermoplastic resin fine particles dispersed in the carrier liquid; a carrier liquid removing means for partially removing the carrier liquid in a layer of the liquid developer on an image carrier which carries an image developed by the developing means; and a transfer means for transferring the image on the image carrier onto a recording medium after partially removing the carrier liquid by the carrier liquid removing means. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、液体現像剤を用いる画像形成装置に関する。   The present invention relates to an image forming apparatus using a liquid developer.

感光体(感光ドラム)に静電潜像を形成し、それにトナーを付着させて、紙などに転写して定着する電子写真方式の画像形成装置が、複写機、MFP(多機能型プリンタ)、FAX、プリンタなどに使用されている。それらの画像形成装置では一般に粉体トナーを用いる乾式のものが広く用いられている。   An electrophotographic image forming apparatus that forms an electrostatic latent image on a photoconductor (photosensitive drum), attaches toner to the photoconductor, and transfers and fixes the image onto paper or the like is a copying machine, an MFP (multifunctional printer), Used for FAX, printer, etc. In these image forming apparatuses, in general, a dry type using powder toner is widely used.

しかし、粉体トナーは、トナーが飛散するという問題点があるとともに、トナー粒子が7〜10μmと大きいことから解像度が悪いという画質上の問題点もある。   However, the powder toner has a problem that the toner is scattered, and also has a problem in image quality that the resolution is poor because the toner particles are as large as 7 to 10 μm.

そこで、大量プリント用のオフィスプリンタやオンデマンド印刷装置などの、より高画質及び高解像度が要求される画像形成装置では、流動パラフィンのような非極性有機溶剤中にトナーを分散させた、液体現像剤を用いる湿式現像方式が用いられるようになっている。液体現像剤は、トナー粒子が1μm程度と小さいとともに、帯電量が大きいことでトナー画像の乱れが起きにくく、高い解像度を実現できるからである。   Therefore, in image forming apparatuses that require higher image quality and higher resolution, such as office printers for mass printing and on-demand printing apparatuses, liquid development in which toner is dispersed in a nonpolar organic solvent such as liquid paraffin A wet development method using an agent is used. This is because the liquid developer has toner particles as small as about 1 μm, and the charge amount is large, so that the toner image is hardly disturbed and high resolution can be realized.

従来の湿式の画像形成装置では、液体現像剤として、キャリア液としての有機溶剤にトナーを1〜2%の割合で混ぜた低粘度の液体現像剤を用いていた。しかしながら、このような現像剤はトナー濃度(以後、現像剤濃度、あるいは単に濃度ともいう)が低いため、紙上へ多量に付着させ定着時に乾燥させることが必要であり、多量の蒸気が発生するといった環境上の大きな問題点をかかえていた。また揮発させるために低沸点のキャリア液しか使用できず、引火点が低いなど安全性においても大きな問題があった。   In a conventional wet image forming apparatus, a low-viscosity liquid developer obtained by mixing a toner in an organic solvent as a carrier liquid at a ratio of 1 to 2% is used as a liquid developer. However, since such a developer has a low toner concentration (hereinafter, also referred to as developer concentration or simply concentration), it is necessary to deposit a large amount on the paper and dry it at the time of fixing, and a large amount of vapor is generated. It had a big environmental problem. Moreover, since only a low boiling point carrier liquid can be used for volatilization, there is a big problem in safety such as a low flash point.

このようなことを背景にして、シリコンオイルなどの不揮発性のキャリア液中に樹脂及び顔料からなる固形分としてのトナーを高濃度に分散させることで構成される、高粘度で高濃度の液体現像剤を用いる画像形成装置が提案されるようになった。この液体現像剤を用いると、上記のような問題の発生が防止され、またトナー濃度が高いことから、大量の液体現像剤を使用しないで済むという利点がある。   Against this background, high-viscosity, high-concentration liquid development is achieved by dispersing toner as a solid component consisting of resin and pigment in a non-volatile carrier liquid such as silicone oil at a high concentration. An image forming apparatus using an agent has been proposed. When this liquid developer is used, the above-described problems can be prevented and the toner concentration is high, so that there is an advantage that it is not necessary to use a large amount of liquid developer.

この液体現像剤を用いて現像する際には、帯電したトナーが絶縁性液体中を静電気の力によって移動して静電潜像を現像する、その移動距離が短いほど現像効率が向上する。そのために、現像ローラ等の現像剤担持体上に現像剤のミクロン単位の薄層を形成し、この薄層化された現像剤を感光体に接触させて現像が行われる。   When developing with this liquid developer, the charged toner moves in the insulating liquid by electrostatic force to develop the electrostatic latent image. The developing efficiency is improved as the moving distance is shorter. For this purpose, a thin layer of a micron unit of developer is formed on a developer carrying member such as a developing roller, and development is performed by bringing the thinned developer into contact with the photoreceptor.

現像により感光体上に形成されたトナー像は記録材に直接転写される、もしくは中間転写体に一次転写の後、記録材に二次転写される。   The toner image formed on the photosensitive member by development is directly transferred to the recording material, or is primarily transferred to the intermediate transfer member and then secondarily transferred to the recording material.

この中間転写体から記録媒体への転写は、電圧印加による静電転写が行われているが、静電転写は記録媒体の電気抵抗に影響されるため、周囲の温度や湿度といった環境要因への依存性が高く、安定した画像が得られにくいと言う問題があった。   The transfer from the intermediate transfer member to the recording medium is performed by electrostatic transfer by applying a voltage. However, since electrostatic transfer is affected by the electrical resistance of the recording medium, it is not affected by environmental factors such as ambient temperature and humidity. There is a problem that the dependency is high and it is difficult to obtain a stable image.

この問題を解決するため、トナーを溶融状態にして粘着力を発生させ、記録媒体に転写する溶融転写定着方式が用いられている。通常溶融転写定着方式は、環境要因への依存度は低くできるが、トナーの粘着力で記録媒体へ転写を行うため、転写圧力を過大にする必要があった。そのため記録媒体が、中間転写体の接触部に噛み込むときに振動が発生し、画像ノイズの原因となっていた。   In order to solve this problem, a melt transfer fixing method is used in which toner is melted to generate an adhesive force and transferred to a recording medium. Normally, the melt transfer fixing method can be less dependent on environmental factors, but the transfer pressure needs to be excessive because the toner is transferred to the recording medium with the adhesive force of the toner. Therefore, vibration occurs when the recording medium bites into the contact portion of the intermediate transfer member, causing image noise.

また、トナー画像の転写時に記録媒体に転写せず、中間転写体に残存したトナーが、過大な圧力がかかることで、中間転写体表面にこびりつき、クリーニング装置でこの残存トナーを除去するのが困難になるという問題もあった。   In addition, the toner remaining on the intermediate transfer member, which is not transferred to the recording medium during transfer of the toner image, is stuck on the surface of the intermediate transfer member due to excessive pressure, and it is difficult to remove the residual toner with a cleaning device. There was also a problem of becoming.

このような問題に対して、特許文献1では、記録媒体への転写前に画像支持体上の液体現像剤をトナーのガラス転移温度よりも高い温度で、且つ、融点よりも低い温度に加熱し、キャリア液除去ローラでトナーの固形分比率を50%〜90%に調整することで、軽微な圧力でも転写媒体への転写効率が良く、強い定着強度が得られるとした方法が提案されている。
特開2003−323053号公報
In order to solve such a problem, in Patent Document 1, the liquid developer on the image support is heated to a temperature higher than the glass transition temperature of the toner and lower than the melting point before transfer to the recording medium. A method has been proposed in which the solid content ratio of the toner is adjusted to 50% to 90% with the carrier liquid removing roller, so that the transfer efficiency to the transfer medium is good and strong fixing strength can be obtained even at a slight pressure. .
JP 2003-323053 A

しかしながら、特許文献1の技術を持ってしても、記録媒体にトナー画像とともにキャリア液が転写されてしまう。この転写されたキャリア液は、記録媒体とトナーとの間に介在するため、十分な定着強度が得られないという問題があった。   However, even with the technique of Patent Document 1, the carrier liquid is transferred to the recording medium together with the toner image. Since the transferred carrier liquid is interposed between the recording medium and the toner, there is a problem that sufficient fixing strength cannot be obtained.

本発明の課題は、不揮発性の液体現像剤を用いた画像形成装置において、画像担持体上の画像を記録媒体に転写する際の転写効率が高く、且つ、定着強度の十分にある画像を形成できる画像形成装置を提供することである。   An object of the present invention is to form an image with high transfer efficiency and sufficient fixing strength when transferring an image on an image carrier to a recording medium in an image forming apparatus using a non-volatile liquid developer. An image forming apparatus is provided.

上記の課題を解決するために、本発明は以下の特徴を有するものである。   In order to solve the above problems, the present invention has the following features.

1.
液体現像剤を用いて現像した画像を記録媒体に転写する画像形成装置において、
不揮発性のキャリア液と、該キャリア液に分散された顔料微粒子と、該キャリア液に分散された熱可塑性の樹脂微粒子とを含む液体現像剤を用いて静電潜像を現像する現像手段と、
該現像手段で顕像化した画像を担持する画像担持体上の液体現像剤の層のキャリア液の一部を除去するキャリア液除去手段と、
該キャリア液除去手段でキャリア液の一部を除去した後の前記画像担持体上の画像を記録媒体に転写する転写手段とを備えたことを特徴とする画像形成装置。
1.
In an image forming apparatus for transferring an image developed using a liquid developer to a recording medium,
Developing means for developing an electrostatic latent image using a liquid developer comprising a non-volatile carrier liquid, pigment fine particles dispersed in the carrier liquid, and thermoplastic resin fine particles dispersed in the carrier liquid;
A carrier liquid removing means for removing a part of the carrier liquid in the layer of the liquid developer on the image carrier that carries the image visualized by the developing means;
An image forming apparatus comprising: transfer means for transferring an image on the image carrier after removing a part of the carrier liquid by the carrier liquid removing means to a recording medium.

2.
前記樹脂微粒子は、前記キャリア液中における体積平均粒径が、10nm以上500nm以下であることを特徴とする1に記載の画像形成装置。
2.
2. The image forming apparatus according to 1, wherein the resin fine particles have a volume average particle diameter in the carrier liquid of 10 nm or more and 500 nm or less.

3.
前記顔料微粒子は、前記キャリア液中における体積平均粒径が、30nm以上500nm以下であることを特徴とする1又は2に記載の画像形成装置。
3.
The image forming apparatus according to 1 or 2, wherein the pigment fine particles have a volume average particle diameter in the carrier liquid of 30 nm or more and 500 nm or less.

4.
前記キャリア液除去手段は、前記画像担持体上の液体現像剤の層に接触し、前記顔料微粒子の帯電極性と同極性の電圧が印加された摺動体であることを特徴とする1乃至3の何れか1項に記載の画像形成装置。
4).
The carrier liquid removing means is a sliding body that is in contact with a liquid developer layer on the image carrier and to which a voltage having the same polarity as the charged polarity of the pigment fine particles is applied. The image forming apparatus according to claim 1.

5.
前記転写手段は、ヒータを有する加熱ローラであることを特徴とする1乃至4の何れか1項に記載の画像形成装置。
5).
5. The image forming apparatus according to claim 1, wherein the transfer unit is a heating roller having a heater.

6.
前記キャリア液除去手段で前記画像担持体上の液体現像剤の層のキャリア液を除去した後、前記転写手段で記録媒体に転写するまでの間で、前記画像担持体上の液体現像剤の層を加熱する加熱手段を有することを特徴とする1乃至5の何れか1項に記載の画像形成装置。
6).
After the carrier liquid in the liquid developer layer on the image carrier is removed by the carrier liquid removing unit, the liquid developer layer on the image carrier is transferred from the carrier liquid to the recording medium by the transfer unit. The image forming apparatus according to any one of 1 to 5, further comprising a heating unit that heats the substrate.

本発明によれば、液体現像剤を用いて現像した画像を記録媒体に転写する画像形成装置において、不揮発性のキャリア液と、該キャリア液に分散された顔料微粒子と、該キャリア液に分散された熱可塑性の樹脂微粒子とを含む液体現像剤を用いて静電潜像を現像する現像手段と、該現像手段で顕像化した画像を担持する画像担持体上の液体現像剤の層のキャリア液の一部を除去するキャリア液除去手段と、該キャリア液除去手段でキャリア液の一部を除去した後の画像担持体上の画像を記録媒体に転写する転写手段とを備えたものとしている。このようにすることで、画像担持体上の画像を記録媒体に転写する際に、転写される画像に含まれるキャリア液の含有量を少なくすることができ、よって、画像担持体上の画像を記録媒体に転写する際の転写効率が高く、且つ、定着強度の十分にある画像を形成できる画像形成装置を提供できる。   According to the present invention, in an image forming apparatus for transferring an image developed using a liquid developer onto a recording medium, a non-volatile carrier liquid, pigment fine particles dispersed in the carrier liquid, and the carrier liquid are dispersed. Developing means for developing an electrostatic latent image using a liquid developer containing fine thermoplastic resin particles, and a carrier for a liquid developer layer on an image carrier for carrying an image visualized by the developing means Carrier liquid removing means for removing a part of the liquid, and transfer means for transferring an image on the image carrier after removing a part of the carrier liquid by the carrier liquid removing means to a recording medium. . In this way, when the image on the image carrier is transferred to the recording medium, the content of the carrier liquid contained in the transferred image can be reduced, and thus the image on the image carrier can be reduced. It is possible to provide an image forming apparatus that can form an image with high transfer efficiency and sufficient fixing strength when transferred to a recording medium.

本発明に係る実施形態を、図を参照して説明する。
(本実施形態に係る画像形成装置の全体構成と動作の例)
図1は、本発明の画像形成装置の一例を示す概略構成図である。ドラム状の感光体201の周囲には、矢印で示す回転方向に順に、帯電装置203、露光装置204、現像ローラ103、中間転写体301、感光体クリーニングブレード202がそれぞれ配設され、中間転写体301の周囲には、1次転写ローラ302、スクイズローラ303、スクイズローラのクリーニングブレード304、2次転写ローラ307、テンションローラ308、ハロゲンヒータ309が配設されている。
Embodiments according to the present invention will be described with reference to the drawings.
(Example of overall configuration and operation of image forming apparatus according to this embodiment)
FIG. 1 is a schematic configuration diagram showing an example of an image forming apparatus of the present invention. Around the drum-shaped photoconductor 201, a charging device 203, an exposure device 204, a developing roller 103, an intermediate transfer body 301, and a photoconductor cleaning blade 202 are arranged in this order in the rotation direction indicated by the arrows. A primary transfer roller 302, a squeeze roller 303, a squeeze roller cleaning blade 304, a secondary transfer roller 307, a tension roller 308, and a halogen heater 309 are disposed around 301.

感光体201の表面を帯電装置203により、所定の表面電位に一様に帯電し、その後、露光装置204により画像情報の露光を行い、感光体201の表面に静電潜像を形成する。次いで、感光体201の静電潜像は、現像剤槽102の液体現像剤104を担持した現像ローラ103により現像することで顕像化され、感光体201の表面にトナー像が形成される。この時現像ローラ103上の液体現像剤は、コロトロン帯電装置105により、帯電させられている。また、現像後の現像ローラ103上の液体現像剤は、クリーニングブレード101により掻きおとされる。   The surface of the photoconductor 201 is uniformly charged to a predetermined surface potential by the charging device 203, and then image information is exposed by the exposure device 204 to form an electrostatic latent image on the surface of the photoconductor 201. Next, the electrostatic latent image on the photoconductor 201 is developed by the developing roller 103 carrying the liquid developer 104 in the developer tank 102, and a toner image is formed on the surface of the photoconductor 201. At this time, the liquid developer on the developing roller 103 is charged by the corotron charging device 105. Further, the liquid developer on the developing roller 103 after development is scraped off by the cleaning blade 101.

液体現像剤は、トナーとしての顔料微粒子と、熱可塑性の樹脂微粒子と、20℃での蒸気圧が200Pa以下の不揮発性液体であるキャリア液とを含んでいる。コロトロン帯電装置105により、顔料微粒子と樹脂微粒子は、同極性に帯電されている。   The liquid developer contains pigment fine particles as a toner, thermoplastic resin fine particles, and a carrier liquid that is a non-volatile liquid having a vapor pressure at 20 ° C. of 200 Pa or less. The pigment fine particles and the resin fine particles are charged to the same polarity by the corotron charging device 105.

また、感光体201上に現像されたトナー像は、トナーだけでなくキャリア液も多く含んでいる状態で感光体201に付着している。   In addition, the toner image developed on the photoconductor 201 is attached to the photoconductor 201 in a state of containing a large amount of carrier liquid as well as toner.

次に感光体201上のトナー像は、1次転写用駆動ローラ302に所定の電圧を印加することによって、画像担持体である中間転写体301に転写される。1次転写用駆動ローラ302にはトナーと逆極性の電圧が印加され、このとき感光体201との電位差は300V〜3kVである。   Next, the toner image on the photosensitive member 201 is transferred to the intermediate transfer member 301 as an image carrier by applying a predetermined voltage to the primary transfer driving roller 302. A voltage having a polarity opposite to that of the toner is applied to the primary transfer driving roller 302. At this time, the potential difference from the photosensitive member 201 is 300 V to 3 kV.

中間転写体301は、図1に示すようにベルト状でも良いし、また、図2に示すようにドラム状の中間転写体301を用いても良い。ドラム状の中間転写体301を用いると、位置精度が出やすく、駆動系を簡易な構成にすることができる。   The intermediate transfer member 301 may have a belt shape as shown in FIG. 1, or a drum-like intermediate transfer member 301 as shown in FIG. When the drum-shaped intermediate transfer member 301 is used, the positional accuracy is easily obtained and the drive system can be simplified.

中間転写体301がベルトの場合、ベルト材質は樹脂や弾性体であり、ラフ紙への転写性を考えると弾性体が望ましく、また耐熱性があるものが望ましい。厚さは50μm以上1mm以下、体積抵抗率は106以上1012Ωcm以下、表面抵抗率は106以上1012Ω/□以下が望ましい。樹脂としては、ポリエステル、ポリプロピレン、ポリアミド、ポリイミド、フッ素系樹脂、ポリフェニルサルフェート等、弾性体としては、シリコンゴム、フッ素ゴム、EPDM、ウレタンゴム、ニトリルゴム等が開示できるが、これに限らない。搬送の安定性を考えると、樹脂基体の上に弾性体がある複層タイプのベルトが望ましい。この場合、樹脂基体の厚さは50〜200μm、弾性体の厚さは200μm〜1mmが望ましい。また、最表層は、離型性が高いことが望まれ、そのため、表層はフッ素系、シリコン系等の低表面エネルギーの重合体や、プラズマ処理等で1μm以下の硬い層を設ける方が好ましい。 In the case where the intermediate transfer member 301 is a belt, the belt material is a resin or an elastic body, and an elastic body is desirable in view of transferability to rough paper, and a material having heat resistance is desirable. Desirably, the thickness is 50 μm or more and 1 mm or less, the volume resistivity is 10 6 or more and 10 12 Ωcm or less, and the surface resistivity is 10 6 or more and 10 12 Ω / □ or less. Examples of the resin include polyester, polypropylene, polyamide, polyimide, fluorine-based resin, polyphenyl sulfate, and the like, and examples of the elastic body include silicon rubber, fluorine rubber, EPDM, urethane rubber, and nitrile rubber, but are not limited thereto. Considering the stability of conveyance, a multilayer belt having an elastic body on a resin substrate is desirable. In this case, the thickness of the resin substrate is desirably 50 to 200 μm, and the thickness of the elastic body is desirably 200 μm to 1 mm. Further, the outermost layer is desired to have high releasability. Therefore, it is preferable that the surface layer is provided with a low surface energy polymer such as fluorine-based or silicon-based or a hard layer of 1 μm or less by plasma treatment or the like.

中間転写体301に転写された画像を含む液体現像剤は、キャリア液の一部を除去する工程として、キャリア液のキャリア液除去手段であるスクイズローラ303により、液体現像剤の層のキャリア液の一部を除去される。スクイズローラ303は、中間転写体301上の液体現像剤の層に接触し、顔料微粒子の帯電極性と同極性の電圧が印加された摺動体である。スクイズローラ303に顔料微粒子と同極性の電圧を印加することにより、顔料微粒子がスクイズローラ303への移動を防止することができる。よって、キャリア液がスクイズローラ303側に移動し、中間転写体301上のキャリア液量はスクイズローラ303を通過後、低減する。スクイズローラ303側に移動したキャリア液は、クリーニングブレード304でクリーニングされる。   In the liquid developer containing the image transferred to the intermediate transfer member 301, as a step of removing a part of the carrier liquid, the squeeze roller 303 which is a carrier liquid removing means for the carrier liquid removes the carrier liquid in the liquid developer layer. Part is removed. The squeeze roller 303 is a sliding body that is in contact with the liquid developer layer on the intermediate transfer body 301 and to which a voltage having the same polarity as the charged polarity of the pigment fine particles is applied. By applying a voltage having the same polarity as the pigment fine particles to the squeeze roller 303, the pigment fine particles can be prevented from moving to the squeeze roller 303. Therefore, the carrier liquid moves to the squeeze roller 303 side, and the amount of carrier liquid on the intermediate transfer member 301 decreases after passing through the squeeze roller 303. The carrier liquid that has moved to the squeeze roller 303 side is cleaned by the cleaning blade 304.

このような手段で記録媒体Pに転写する前に画像担持体である中間転写体301上の液体現像剤のキャリア液量が低減される。キャリア液量の低減により、液体現像剤中のトナー粒子同士が接触し、さらに密着してフィルム化される。この時の様子を図3(a)、(b)を用いて、従来の液体現像剤を用いた場合(a)と本発明の液体現像剤を用いた場合(b)を比較して、説明する。   The carrier liquid amount of the liquid developer on the intermediate transfer member 301 as an image carrier is reduced before being transferred to the recording medium P by such means. By reducing the amount of the carrier liquid, the toner particles in the liquid developer come into contact with each other and are further closely adhered to form a film. The situation at this time will be described with reference to FIGS. 3A and 3B, comparing the case where the conventional liquid developer is used (a) and the case where the liquid developer of the present invention is used (b). To do.

従来のトナー粒子は、バインダー樹脂の中に顔料を分散させた粒子を用いており、比較的大きい粒径のものである。スクイズローラ303によるキャリア除去を行った場合、図3(a)から分かるように従来の顕像化されたトナー像は、粒子間にキャリア液が多く残る。これに比べ本発明の液体現像剤では、図3(b)に示すようにトナーとして顔料微粒子そのものを用いているため、画像担持体上に緻密に付着し、また、熱可塑性の樹脂微粒子を分散しているので、顔料微粒子同士の間に樹脂微粒子が入った状態となる。このため、粒子間の間のキャリア液量が更に少なくなり、トナー像の固形分比率を少なくすることができる。また、顔料微粒子と樹脂微粒子とが密着することで互いに付着力が生じて、フィルム化した状態になる。   Conventional toner particles use particles in which a pigment is dispersed in a binder resin, and have a relatively large particle size. When the carrier is removed by the squeeze roller 303, as can be seen from FIG. 3A, in the conventional toner image that has been visualized, a large amount of carrier liquid remains between the particles. In contrast, the liquid developer of the present invention uses pigment fine particles themselves as a toner as shown in FIG. 3B, so that they adhere closely to the image carrier and also disperse the thermoplastic resin fine particles. As a result, resin fine particles enter between the pigment fine particles. For this reason, the amount of the carrier liquid between the particles is further reduced, and the solid content ratio of the toner image can be reduced. Further, when the pigment fine particles and the resin fine particles are brought into close contact with each other, an adhesive force is generated and a film is formed.

このような状態で、中間転写体301上の画像を加熱手段であるハロゲンヒータ309で加熱する。加熱することにより樹脂微粒子を軟化又は溶融状態にし、次の転写工程に移る。   In this state, the image on the intermediate transfer member 301 is heated by a halogen heater 309 as a heating unit. The resin fine particles are softened or melted by heating, and the process proceeds to the next transfer step.

記録媒体に転写する工程としては、転写手段としてのヒータを内蔵した加熱ローラである転写ローラ307及びバックアップローラ306を用いて、トナー像を記録部材Pに溶融熱転写する。この時の転写効率は、ほぼ100%で、転写後の定着性能も向上し、定着強度の強い画像を形成することができる。   In the process of transferring to the recording medium, the toner image is melted and transferred to the recording member P using a transfer roller 307 and a backup roller 306 which are heating rollers incorporating a heater as a transfer means. The transfer efficiency at this time is almost 100%, the fixing performance after transfer is improved, and an image having a high fixing strength can be formed.

スクイズローラ303は、内部に加熱手段を有し、中間転写体301上の液体現像剤を加熱するのが好ましい。また、バックアップローラ305も加熱手段を有しても良い。   The squeeze roller 303 preferably has a heating means inside, and heats the liquid developer on the intermediate transfer member 301. The backup roller 305 may also have a heating unit.

スクイズローラ303はアスカーA硬度20度から90度の弾性体である。弾性体としては、シリコンゴム、フッ素ゴム、EPDM、ウレタンゴム、ニトリルゴム等が開示できるが、これに限らない。スクイズローラ303を加熱する場合、80℃から200℃程度に加熱すれば良い。また、記録媒体Pに転写する前にこのようなスクイズローラ303を複数個配置しても良い。また、ハロゲンヒータ309のように記録媒体Pに転写する前に中間転写体301を加熱する手段は、省いても良い。   The squeeze roller 303 is an elastic body having an Asker A hardness of 20 degrees to 90 degrees. As the elastic body, silicon rubber, fluorine rubber, EPDM, urethane rubber, nitrile rubber, and the like can be disclosed, but not limited thereto. When the squeeze roller 303 is heated, it may be heated from about 80 ° C. to about 200 ° C. Further, a plurality of such squeeze rollers 303 may be arranged before transferring to the recording medium P. Further, a means for heating the intermediate transfer member 301 before transfer to the recording medium P, such as the halogen heater 309, may be omitted.

このように記録部材Pに転写する前に中間転写体301上のトナー像を加熱することにより、よりトナー像がフィルム化し、転写効率が100%に近づけることができる。   Thus, by heating the toner image on the intermediate transfer body 301 before transferring to the recording member P, the toner image becomes a film, and the transfer efficiency can approach 100%.

転写手段として、熱転写を用いたが、電界転写、ずり転写を用いたものでも良く、特に制約はないが、この中では熱転写が好ましい。熱転写を用いる場合、転写ローラ307やバックアップローラ306に加熱手段を有する。この場合、加熱温度は80℃以上200℃以下が好ましい。バックアップローラ307はアスカーA硬度が20℃以上90℃以下の弾性体で、弾性体としては、シリコンゴム、フッ素ゴム、EPDM、ウレタンゴム、ニトリルゴム等が開示できるが、これに限らない。   As the transfer means, thermal transfer is used, but electric transfer or shear transfer may be used. There is no particular limitation, but thermal transfer is preferable. When thermal transfer is used, the transfer roller 307 and the backup roller 306 have heating means. In this case, the heating temperature is preferably 80 ° C. or higher and 200 ° C. or lower. The backup roller 307 is an elastic body having an Asker A hardness of 20 ° C. or higher and 90 ° C. or lower. As the elastic body, silicon rubber, fluorine rubber, EPDM, urethane rubber, nitrile rubber, or the like can be disclosed, but not limited thereto.

記録媒体Pに転写後、中間転写体301は冷却部材310のような冷却工程を有する方が望ましい。冷却部材310としては、冷却ファンなどを用いることができる。中間転写体301を冷却部材310を用いて冷却することにより、熱が感光体201に伝わることを防止し、感光体201の耐久性を上げることができる。   After the transfer to the recording medium P, it is desirable that the intermediate transfer member 301 has a cooling process like the cooling member 310. As the cooling member 310, a cooling fan or the like can be used. By cooling the intermediate transfer member 301 using the cooling member 310, heat is prevented from being transmitted to the photosensitive member 201, and the durability of the photosensitive member 201 can be improved.

なお、上記実施形態では、画像担持体として中間転写体301を用いて説明したが、中間転写体301を用いずに、感光体201上の画像を記録媒体Pに直接転写する構成であっても良い。この場合、画像担持体は感光体201となる。
(液体現像剤の構成)
液体現像剤は、少なくともキャリア液、顔料微粒子、分散剤、樹脂微粒子から構成される。
In the above embodiment, the intermediate transfer member 301 is used as the image carrier. However, the image on the photosensitive member 201 may be directly transferred to the recording medium P without using the intermediate transfer member 301. good. In this case, the image carrier is the photosensitive member 201.
(Configuration of liquid developer)
The liquid developer is composed of at least a carrier liquid, pigment fine particles, a dispersant, and resin fine particles.

キャリア液は、不揮発性であって、20℃での蒸気圧は200Pa以下で、誘電率は3以下の低誘電率であり、電気的絶縁性は高いものが選択される。例えば、炭化水素系(流動パラフィン)、シリコンオイル、動植物油、鉱物油、等から選ばれる。   The carrier liquid is non-volatile, has a vapor pressure at 20 ° C. of 200 Pa or less, a low dielectric constant of 3 or less, and a high electrical insulation property. For example, it is selected from hydrocarbons (liquid paraffin), silicon oil, animal and vegetable oils, mineral oils, and the like.

本発明の顔料微粒子としては、ファーネストブラック、ランプブラック、アセチレンブラック、チャンネルブラック、C.I.ピグメントブラック、オルトアニリンブラック、トルイジンオレンジ、パーマネントカーミンFB、ファーストイエローAAA、ジスアゾオレンジPMP、レーキレッドC、ブリリアントカーミン6B、フタロシアニンブルー、キナクリドンレッド、C.I.ピグメントブルー、C.I.ピグメントレッド、C.I.ピグメントイエロー、ジオキサンバイオレット、ピクトリアピュアブルー、アルカリブルートナー、アルカリブルーRトナー、ファーストイエロー10G、オルトニトロアニリンオレンジ、トルイジンレッド、バリウムレッド2B、カルシウムレッド2B、ピグメントスカーレッド3Bレーキ、アンソシン3Bレーキ、ローダミン6Bレーキ、メチルバイオレットレーキ、ベーシックブルー6Bレーキ、ファーストスカイブルー、レフレックスブルーG、ブリリアントグリーンレーキ、銅フタロシアニン、フタロシアニングリーンG、紺青、群青、酸化鉄粉、亜鉛華、炭酸カルシウム、クレー、硫酸バリウム、アルミナホワイト、アルミニウム粉、昼光蛍光顔料、パール顔料等が挙げられる。   Examples of the pigment fine particles of the present invention include furnace black, lamp black, acetylene black, channel black, C.I. I. Pigment Black, Orthoaniline Black, Toluidine Orange, Permanent Carmine FB, First Yellow AAA, Disazo Orange PMP, Lake Red C, Brilliant Carmine 6B, Phthalocyanine Blue, Quinacridone Red, C.I. I. Pigment blue, C.I. I. Pigment Red, C.I. I. Pigment Yellow, Dioxane Violet, Pictoria Pure Blue, Alkali Blue Toner, Alkali Blue R Toner, First Yellow 10G, Ortho Nitroaniline Orange, Toluidine Red, Barium Red 2B, Calcium Red 2B, Pigment Scar Red 3B Lake, Anthosine 3B Lake, Rhodamine 6B rake, methyl violet rake, basic blue 6B rake, first sky blue, reflex blue G, brilliant green rake, copper phthalocyanine, phthalocyanine green G, bitumen, ultramarine, iron oxide powder, zinc white, calcium carbonate, clay, sulfuric acid Examples include barium, alumina white, aluminum powder, daylight fluorescent pigment, and pearl pigment.

また、顔料微粒子の分散性を向上させるため、顔料誘導体を用いても良い。所望の官能基、例えばカルボキシル基、スルホン酸基、水酸基、アミノ基、アミド基等を有した顔料誘導体を使用することができる。   In order to improve the dispersibility of the pigment fine particles, a pigment derivative may be used. A pigment derivative having a desired functional group such as a carboxyl group, a sulfonic acid group, a hydroxyl group, an amino group, or an amide group can be used.

顔料微粒子は、キャリア液に分散され、その二次粒径は、体積平均粒径が30nm以上500nm以下であることが好ましく、より好ましくは、50nm以上300nm以下が良い。このような粒径にすることで、顔料微粒子間の隙間を少なくすることができる。30nm未満では、樹脂微粒子と同じように感光体201への現像性が低下する傾向にある。また、500nmを越えると、先の述べるキャリア液除去手段におけるキャリア液の除去の効果が減少する傾向がある。   The pigment fine particles are dispersed in the carrier liquid, and the secondary particle size thereof is preferably 30 nm or more and 500 nm or less, more preferably 50 nm or more and 300 nm or less. By setting it as such a particle size, the clearance gap between pigment fine particles can be decreased. If the thickness is less than 30 nm, the developability on the photosensitive member 201 tends to be reduced as in the case of the resin fine particles. On the other hand, if it exceeds 500 nm, the effect of removing the carrier liquid in the carrier liquid removing means described above tends to decrease.

顔料微粒子の配合量は、キャリア液量に対して3質量%以上30質量%以下が良い。3質量%以下では所望の濃度が得られず、30質量%以上では分散性を損なう恐れがある。   The blending amount of the pigment fine particles is preferably 3% by mass or more and 30% by mass or less with respect to the carrier liquid amount. If it is 3% by mass or less, the desired concentration cannot be obtained, and if it is 30% by mass or more, the dispersibility may be impaired.

顔料微粒子の分散剤は、水酸基含有カルボン酸エステル、長鎖ポリアミノアマイドと高分子量酸エステル塩、高分子量ポリカルボン酸の塩、長鎖ポリアミノアマイドと極性酸エステルの塩、高分子量不飽和酸エステル、高分子共重合物、変性ポリウレタン、変性ポリアクリレート、ポリエーテルエステル型アニオン系活性剤、ナフタレンスルホン酸ホルマリン縮合物塩、芳香族スルホン酸ホルマリン縮合物塩、ポリオキシエチレンアルキルリン酸エステル、ポリオキシエチレンノニルフェニルエーテル、ポリエステルポリアミン、ステアリルアミンアセテート等を用いることができる。   The dispersant for the pigment fine particles includes hydroxyl group-containing carboxylic acid ester, long chain polyaminoamide and high molecular weight acid ester salt, high molecular weight polycarboxylic acid salt, long chain polyaminoamide and polar acid ester salt, high molecular weight unsaturated acid ester, Polymer copolymer, modified polyurethane, modified polyacrylate, polyether ester type anionic activator, naphthalene sulfonic acid formalin condensate salt, aromatic sulfonic acid formalin condensate salt, polyoxyethylene alkyl phosphate ester, polyoxyethylene Nonylphenyl ether, polyester polyamine, stearylamine acetate and the like can be used.

顔料微粒子の分散剤の量は顔料微粒子に対して10質量%以上200質量%以下が好ましい。   The amount of the pigment fine particle dispersant is preferably 10% by mass or more and 200% by mass or less based on the pigment fine particles.

必要な分散剤量は顔料微粒子の粒径によって異なり、小粒径にしたければ多く配合することが望ましい。10質量%以下では分散性を損ない、200質量%以上では液の導電性が上がり、帯電性を損なう恐れがある。   The amount of dispersant required varies depending on the particle size of the pigment fine particles, and it is desirable to add a large amount if a small particle size is desired. If it is 10% by mass or less, the dispersibility is impaired, and if it is 200% by mass or more, the conductivity of the liquid increases and the chargeability may be impaired.

顔料微粒子の分散剤は、高分子系の顔料分散剤の使用が好ましい。高分子系の顔料分散剤は有機溶媒と相溶性を上げるための長鎖のアルキル基と顔料との吸着のための酸もしくは塩基性の官能基を有している。好ましい分散剤は、顔料によって異なり、顔料の酸、塩基性とは逆と酸、塩基性を有した顔料分散剤を選ぶことが好ましい。   The pigment fine particle dispersant is preferably a polymer pigment dispersant. The polymer pigment dispersant has a long-chain alkyl group for increasing compatibility with an organic solvent and an acid or basic functional group for adsorption of the pigment. A preferable dispersant varies depending on the pigment, and it is preferable to select a pigment dispersant having an acid or basicity opposite to the acid or basicity of the pigment.

樹脂微粒子は、熱可塑性でガラス転移点−10℃以上60℃以下が好ましい。   The resin fine particles are thermoplastic and preferably have a glass transition point of −10 ° C. or higher and 60 ° C. or lower.

樹脂微粒子は、キャリア液に分散され、その二次粒径は、体積平均粒径が10nm以上500nm以下であることが好ましく、より好ましくは、50nm以上300nm以下が良い。このような粒径にすることで、顔料微粒子の間に充填されやすくなり、よりキャリア液の除去を行うことができる。10nm未満では、製造上得られにくいことや、微粒子の電界による移動性に制約がでてきて、感光体201への現像性が低下する傾向がある。また、粒径500nmを超えると、微粒子が凝集しやすくなることや、先の述べるキャリア液除去手段におけるキャリア液の除去の効果が減少する傾向がある。   The resin fine particles are dispersed in the carrier liquid, and the secondary particle size thereof is preferably 10 nm or more and 500 nm or less, and more preferably 50 nm or more and 300 nm or less. By setting it as such a particle diameter, it becomes easy to fill between pigment fine particles, and can remove a carrier liquid more. If the thickness is less than 10 nm, it is difficult to obtain in production, and the mobility of fine particles due to the electric field is restricted, and the developability to the photosensitive member 201 tends to be lowered. On the other hand, when the particle diameter exceeds 500 nm, the fine particles tend to aggregate and the effect of removing the carrier liquid in the carrier liquid removing means described above tends to decrease.

樹脂微粒子としては、市販の樹脂微粒子を用いることができる。また、樹脂微粒子を貧溶媒に分散した非水系分散体(NAD)をキャリア液と混合して使用することもできる。   Commercially available resin fine particles can be used as the resin fine particles. Further, a non-aqueous dispersion (NAD) in which resin fine particles are dispersed in a poor solvent can be used by mixing with a carrier liquid.

NADは溶媒に不要な樹脂分散相と高分子分散安定剤とから構成される。樹脂分散相の一例として、ラジカル重合したアクリル系ポリマーが提示できる。NADの高分子分散安定剤は、数平均分子量1000以上の高分子で、高分子分散剤は樹脂分散相との結合活性点を有し、架橋、接着に必要な官能基を有している。NADの高分子分散剤として、アクリル樹脂、ポリエステル樹脂、アルキド樹脂、メラミン樹脂、セルロース誘導体、等に水酸基、カルボキシル基、グリシジル基、アミノ基、アミド基等の官能基を導入したものが好ましい。樹脂分散相のガラス転移点は−10℃以上60℃以下であることが望ましい。−10℃以下では、保管安定性が悪くなり、60℃以上では定着性に問題が生じる恐れがある。NAD分散相のような小径で極性基を多く有した分散相は、先行例のような一般的な液体現像剤に比べて、液体状態での安定性が高く、より低Tg化が可能で、低温定着しやすい。また、NAD分散相は必要に応じて粒子同士もしくは粒子内が反応するように、反応性の官能基を有しても良い。   NAD is composed of a resin dispersed phase unnecessary for a solvent and a polymer dispersion stabilizer. As an example of the resin dispersed phase, a radical polymerized acrylic polymer can be presented. The polymer dispersion stabilizer of NAD is a polymer having a number average molecular weight of 1000 or more, and the polymer dispersant has a binding active point with the resin dispersed phase and has a functional group necessary for crosslinking and adhesion. As the NAD polymer dispersant, an acrylic resin, a polyester resin, an alkyd resin, a melamine resin, a cellulose derivative, or the like into which a functional group such as a hydroxyl group, a carboxyl group, a glycidyl group, an amino group, or an amide group is introduced is preferable. The glass transition point of the resin dispersed phase is desirably -10 ° C or higher and 60 ° C or lower. If it is −10 ° C. or lower, the storage stability is deteriorated, and if it is 60 ° C. or higher, there is a possibility that a problem occurs in the fixing property. A dispersed phase having a small diameter and a large number of polar groups, such as an NAD dispersed phase, has higher stability in a liquid state and can have a lower Tg than a general liquid developer such as the preceding example. Easy to fix at low temperature. Further, the NAD dispersed phase may have a reactive functional group so that the particles or the inside of the particles react as necessary.

樹脂微粒子(固形分)の配合量は、顔料微粒子に対して0.5倍以上20倍以下が好ましい。0.5倍以下では、定着性を損ない、20倍を超えると、粘度が上昇し、現像性を損なう恐れがある。   The blending amount of the resin fine particles (solid content) is preferably 0.5 to 20 times the pigment fine particles. If it is 0.5 times or less, the fixability is impaired, and if it exceeds 20 times, the viscosity increases and the developability may be impaired.

液体現像剤の製造法として、顔料微粒子を溶媒に分散した分散体と、樹脂微粒子を溶媒に分散した分散体を個別に作り、混合しても良いし、顔料微粒子の存在下で樹脂微粒子を重合し分散体としてもかまわない。   As a method for producing a liquid developer, a dispersion in which pigment fine particles are dispersed in a solvent and a dispersion in which resin fine particles are dispersed in a solvent may be separately prepared and mixed, or the resin fine particles are polymerized in the presence of the pigment fine particles. However, it may be a dispersion.

1.液体現像剤Aの製造
(キャリア液への顔料の分散調整)
顔料:酸性処理した銅フタロシアニンの誘導体 12質量部
分散剤:塩基性の顔料分散剤ソルスパーズ13940(アビシア社製) 5質量部
キャリア液:流動パラフィン(蒸気圧約30Pa、引火点144℃) 100質量部
を混合し、ジルコニアビーズ100質量部とともにペイントコンディショナーにて24時間攪拌し、ビーズを除去して、顔料分散液1を得た。顔料分散液1の顔料微粒子の粒径を粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径が120nmであった。
(キャリア液への樹脂微粒子の分散調整)
まず、樹脂微粒子の分散剤Aを次のように作成した。
1. Production of liquid developer A (dispersion adjustment of pigment in carrier liquid)
Pigment: Acid-treated copper phthalocyanine derivative 12 parts by weight Dispersant: Basic pigment dispersant Solspers 13940 (manufactured by Avicia) 5 parts by weight Carrier liquid: Liquid paraffin (vapor pressure about 30 Pa, flash point 144 ° C.) 100 parts by weight are mixed Then, the mixture was stirred with a paint conditioner for 24 hours together with 100 parts by mass of zirconia beads, and the beads were removed to obtain pigment dispersion 1. When the particle size of the pigment fine particles of the pigment dispersion 1 was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), the volume average particle size was 120 nm.
(Dispersion adjustment of resin fine particles in carrier liquid)
First, a dispersant A for resin fine particles was prepared as follows.

攪拌装置、温度計、反応生成除去装置および窒素ガス導入管を備えた4つ口フラスコに、キャリア液と同じ流動パラフィン100質量部とAIBN1質量部を仕込み、120℃に昇温し、モノマー状態のメチルメタクリレート25質量部、ラウリルメタクリレート55質量部、ヒドロキシエチルメタクリレート19質量部、アクリル酸1質量部を加え、この混合物を4時間かけて滴下した。これを減圧蒸留し、不揮発分40%の分散剤Aを得た。   In a four-necked flask equipped with a stirrer, thermometer, reaction product removal apparatus and nitrogen gas introduction tube, 100 parts by mass of liquid paraffin and AIBN 1 part by mass, which are the same as the carrier liquid, are charged and heated to 120 ° C. 25 parts by mass of methyl methacrylate, 55 parts by mass of lauryl methacrylate, 19 parts by mass of hydroxyethyl methacrylate and 1 part by mass of acrylic acid were added, and this mixture was added dropwise over 4 hours. This was distilled under reduced pressure to obtain Dispersant A having a nonvolatile content of 40%.

次にこの分散剤Aを用いて、キャリア液に分散した樹脂微粒子分散液1を次のように調整した。   Next, using this dispersant A, a resin fine particle dispersion 1 dispersed in a carrier liquid was prepared as follows.

樹脂微粒子の原料として、メチルメタクリレート35質量部、ヒドロキシエチルメタクリレート12質量部、グリシジルメタクリレート2質量部、アクリル酸1質量部、を加え、更に、AIBN1質量部を加えて、混合物とした。この混合物を、分散剤Aを30質量部、キャリア液としての流動パラフィン70質量部を入れ、100℃まで加熱した4つ口フラスコに、4時間かけて滴下した。さらにAIBN0.5質量部と流動パラフィン8質量部の混合物を上記フラスコに加え、減圧蒸留し、固形分50%の白濁した、樹脂微粒子分散液1を得た。樹脂微粒子の粒径を粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径が100nmであった。
(液体現像剤Aの調整)
顔料分散液1を100質量部、樹脂微粒子分散液1を50質量部混合し、液体現像剤Aを得た。
2.液体現像剤Bの製造
(キャリア液への顔料の分散調整)
顔料:塩基性処理した銅フタロシアニンの誘導体 8質量部
分散剤:酸性の顔料分散剤ソルスパーズ3000(アビシア社製) 5質量部
キャリア液:流動パラフィン(蒸気圧約10Pa、引火点144℃) 100質量部
を混合し、ジルコニアビーズ100質量部とともにペイントコンディショナーにて24時間攪拌し、ビーズを除去して、顔料分散液2を得た。顔料分散液2の顔料微粒子の粒径を粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径が300nmであった。
(キャリア液への樹脂微粒子の分散調整)
液体現像剤Aで使用した樹脂微粒子分散液1を用いた。
(液体現像剤Bの調整)
顔料分散液2を100質量部、樹脂微粒子分散液1を40質量部混合し、液体現像剤Bを得た。
3.液体現像剤Cの製造
(キャリア液への顔料の分散調整)
顔料:カーボンブラック(MA−100、三菱化学) 8質量部
分散剤:塩基性の顔料分散剤ソルスパーズ13940(アビシア社製) 4質量部
キャリア液:流動パラフィン(蒸気圧約10Pa、引火点144℃) 100質量部
を混合し、ジルコニアビーズ100質量部とともにペイントコンディショナーにて24時間攪拌し、ビーズを除去して、顔料分散液3を得た。顔料分散液3の顔料微粒子の粒径を粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径が80nmであった。
(キャリア液への樹脂微粒子の分散調整)
アクリル系樹脂微粒子40質量部をキャリア液としての流動パラフィン60質量部に分散した市販の樹脂分散液(アクリディックYL−431、大日本インキ)を用い、樹脂微粒子分散液3とした。樹脂微粒子の粒径を粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径は50nmであった。
(液体現像剤Cの調整)
顔料分散液3を100質量部、樹脂微粒子分散液3を40質量部混合し、液体現像剤Cを得た。
4.液体現像剤Dの製造
液体現像剤Cの製造において、市販の樹脂分散液をニッセツU3611(日本カーバイド社製)とした他は液体現像剤Cと同じようにして作成し、液体現像剤Dとした。樹脂微粒子の粒径は、粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径は300μmであった。
5.液体現像剤Eの製造
液体現像剤Aの製造において、分散剤のS13940を2.5質量部とした他は液体現像剤Aと同じようにして作成し、液体現像剤Eとした。この時の顔料微粒子の粒径は、粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径1.5μmであった。
6.液体現像剤Fの製造
スチレンアクリル共重合体(スチレン:ブチルメタクリレート:メチルメタクリレート=70:25:5、Mn=5300、Mw=23500)100質量部、銅フタロシアニン10質量部を混合し、ヘンシェルミキサーにて十分混合し、二軸押出混練機で溶融混合後、冷却しその後、粗粉砕しジェット粉砕機にて体積平均粒径10μmに微粉砕し、顔料樹脂微粒子とした。
As raw materials for the resin fine particles, 35 parts by mass of methyl methacrylate, 12 parts by mass of hydroxyethyl methacrylate, 2 parts by mass of glycidyl methacrylate and 1 part by mass of acrylic acid were added, and further 1 part by mass of AIBN was added to obtain a mixture. 30 parts by mass of dispersant A and 70 parts by mass of liquid paraffin as a carrier liquid were added to this mixture, and the mixture was added dropwise to a four-necked flask heated to 100 ° C. over 4 hours. Further, a mixture of 0.5 parts by weight of AIBN and 8 parts by weight of liquid paraffin was added to the flask and distilled under reduced pressure to obtain a resin fine particle dispersion 1 having a solid content of 50% and becoming cloudy. When the particle size of the resin fine particles was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), the volume average particle size was 100 nm.
(Adjustment of liquid developer A)
100 parts by mass of the pigment dispersion 1 and 50 parts by mass of the resin fine particle dispersion 1 were mixed to obtain a liquid developer A.
2. Production of liquid developer B (dispersion adjustment of pigment in carrier liquid)
Pigment: Derivative of copper phthalocyanine treated with a basic treatment 8 parts by weight Dispersant: Acid pigment dispersant Solspers 3000 (manufactured by Avicia) 5 parts by weight Carrier liquid: Liquid paraffin (vapor pressure about 10 Pa, flash point 144 ° C.) 100 parts by weight are mixed Then, the mixture was stirred for 24 hours with a paint conditioner together with 100 parts by mass of zirconia beads, and the beads were removed to obtain a pigment dispersion 2. When the particle size of the pigment fine particles of the pigment dispersion 2 was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), the volume average particle size was 300 nm.
(Dispersion adjustment of resin fine particles in carrier liquid)
The resin fine particle dispersion 1 used in the liquid developer A was used.
(Adjustment of liquid developer B)
100 parts by mass of the pigment dispersion 2 and 40 parts by mass of the resin fine particle dispersion 1 were mixed to obtain a liquid developer B.
3. Production of liquid developer C (dispersion adjustment of pigment in carrier liquid)
Pigment: Carbon black (MA-100, Mitsubishi Chemical) 8 parts by mass Dispersant: Basic pigment dispersant Solspers 13940 (manufactured by Abyssia) 4 parts by mass Carrier liquid: Liquid paraffin (vapor pressure about 10 Pa, flash point 144 ° C.) 100 parts by mass Parts were mixed and stirred with a paint conditioner for 24 hours together with 100 parts by mass of zirconia beads, and the beads were removed to obtain pigment dispersion 3. When the particle size of the pigment fine particles of the pigment dispersion 3 was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), the volume average particle size was 80 nm.
(Dispersion adjustment of resin fine particles in carrier liquid)
A resin fine particle dispersion 3 was prepared using a commercially available resin dispersion (Acridic YL-431, Dainippon Ink) in which 40 parts by mass of acrylic resin fine particles were dispersed in 60 parts by mass of liquid paraffin as a carrier liquid. When the particle size of the resin fine particles was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), the volume average particle size was 50 nm.
(Adjustment of liquid developer C)
100 parts by mass of the pigment dispersion 3 and 40 parts by mass of the resin fine particle dispersion 3 were mixed to obtain a liquid developer C.
4). Production of liquid developer D In the production of liquid developer C, liquid developer D was prepared in the same manner as liquid developer C except that a commercially available resin dispersion was used as Nisset U3611 (manufactured by Nippon Carbide). . The particle size of the resin fine particles was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), and the volume average particle size was 300 μm.
5). Production of liquid developer E Liquid developer E was prepared in the same manner as liquid developer A except that S13940 of the dispersant was changed to 2.5 parts by mass in the production of liquid developer A. The particle size of the pigment fine particles at this time was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), and the volume average particle size was 1.5 μm.
6). Production of liquid developer F 100 parts by mass of styrene acrylic copolymer (styrene: butyl methacrylate: methyl methacrylate = 70: 25: 5, Mn = 5300, Mw = 23500) and 10 parts by mass of copper phthalocyanine were mixed into a Henschel mixer. The mixture was melted and mixed with a twin screw extruder kneader, cooled, then coarsely pulverized, and finely pulverized to a volume average particle diameter of 10 μm with a jet pulverizer to obtain pigment resin fine particles.

この顔料樹脂微粒子を20質量部、分散剤としてソルスパーズS13940を3質量部、キャリア液としての流動パラフィン100質量部(蒸気圧約5Pa、引火点200℃)、ジルコニアビーズ100質量部を混合し、サンドミルにて120時間攪拌し、液体現像剤Fを得た。顔料樹脂微粒子の粒径は、粒度分布計(島津製作所製、SALD−2200)にて測定したところ、体積平均粒径は2μmであった。
(実施例1)
図1に示す画像形成装置を使用し、定着性の評価を行った。感光体201は直径100mmのアルミドラムに有機感光体膜(膜厚35μm)を形成したものであり、回転周速を200mm/secに設定した。液体現像剤は現像ローラ103上でコロトロン帯電装置105によって5kVに印加されたチャージワイヤーからの放電によりプラスに帯電させられている。帯電装置203はスコロトロンチャージャーを用い、感光体201の表面電位が600Vになるようにした。露光装置204は半導体レーザで画像部分を露光した時に感光体201の表面電位が100Vとなるように設定し、現像ローラ103には400V電圧を印加した。
20 parts by mass of the pigment resin fine particles, 3 parts by mass of Solspers S13940 as a dispersant, 100 parts by mass of liquid paraffin as a carrier liquid (vapor pressure of about 5 Pa, flash point 200 ° C.), and 100 parts by mass of zirconia beads are mixed in a sand mill. For 120 hours to obtain a liquid developer F. The particle diameter of the pigment resin fine particles was measured with a particle size distribution meter (SALD-2200, manufactured by Shimadzu Corporation), and the volume average particle diameter was 2 μm.
Example 1
The image forming apparatus shown in FIG. 1 was used to evaluate the fixability. The photoconductor 201 is formed by forming an organic photoconductor film (film thickness: 35 μm) on an aluminum drum having a diameter of 100 mm, and the rotational peripheral speed was set to 200 mm / sec. The liquid developer is positively charged on the developing roller 103 by the discharge from the charge wire applied to 5 kV by the corotron charging device 105. The charging device 203 was a scorotron charger, and the surface potential of the photoconductor 201 was set to 600V. The exposure device 204 was set so that the surface potential of the photosensitive member 201 was 100 V when the image portion was exposed with a semiconductor laser, and a 400 V voltage was applied to the developing roller 103.

液体現像剤としては現像剤Aを用い、画像パターンとしてソリッドパターン(100ベタ)を印字し、このとき現像ローラ103上の現像剤量7.5g/m2に調整した。(固形分20%)
1次転写ローラ302には−800V電圧を印加した。
Developer A was used as the liquid developer, and a solid pattern (100 solids) was printed as an image pattern. At this time, the developer amount on the developing roller 103 was adjusted to 7.5 g / m 2 . (Solid content 20%)
A voltage of −800 V was applied to the primary transfer roller 302.

中間転写体301は、100μmのポリイミド樹脂上に厚さ500μmのシリコンゴムを持った複層構成のものを用いた。1次転写ローラ302直後の301上の現像剤量は5g/m2(固形分30%)であった。スクイズローラ303は直径30mmでアスカーA硬度40℃のシリコンローラである。ここで、スクイズローラ303にヒータを設置し、液体現像剤中の樹脂成分を溶融させた方がスクイズの効率は向上する。加熱温度はスクイズローラ303の表面温度が120℃になるように加熱されている。また、スクイズローラ303には1000V電圧が印加されている。キャリア液除去ブレード304は金属ブレードで、スクイズローラ303で回収したキャリア液がキャリア液除去ブレード304で除去される。スクイズローラ303通過後の現像剤量は1.8g/m2(固形分83%)であった。 As the intermediate transfer member 301, a multi-layer structure having a silicon rubber with a thickness of 500 μm on a polyimide resin with a thickness of 100 μm was used. The amount of developer on 301 immediately after the primary transfer roller 302 was 5 g / m 2 (solid content 30%). The squeeze roller 303 is a silicon roller having a diameter of 30 mm and an Asker A hardness of 40 ° C. Here, the squeeze efficiency is improved by installing a heater in the squeeze roller 303 and melting the resin component in the liquid developer. The heating temperature is heated so that the surface temperature of the squeeze roller 303 is 120 ° C. In addition, a voltage of 1000 V is applied to the squeeze roller 303. The carrier liquid removal blade 304 is a metal blade, and the carrier liquid collected by the squeeze roller 303 is removed by the carrier liquid removal blade 304. The developer amount after passing through the squeeze roller 303 was 1.8 g / m 2 (solid content 83%).

加熱手段309は、中間転写体301の表面を加熱し、中間転写体301上の現像剤中の樹脂成分を溶融する。2次転写ローラ307の温度は140℃で、アスカーA硬度40度のシリコンゴムローラである。2次転写ローラ307を用いて記録媒体Pとしての王子製紙社製OKトップコート紙に現像剤を転写し定着した。
(実施例2〜5)
実施例2〜5においては、実施例1の現像剤Aに代えて、現像剤B〜Eを使用した他は、実施例1と同様に行い、評価した。
(比較例1)
比較例1においては、実施例1の現像剤Aに代えて、現像剤Fを使用した他は、実施例1と同様に行い、評価した。
The heating unit 309 heats the surface of the intermediate transfer member 301 and melts the resin component in the developer on the intermediate transfer member 301. The secondary transfer roller 307 is a silicon rubber roller having a temperature of 140 ° C. and an Asker A hardness of 40 degrees. Using the secondary transfer roller 307, the developer was transferred and fixed on OK top coat paper manufactured by Oji Paper Co. as the recording medium P.
(Examples 2 to 5)
In Examples 2 to 5, evaluation was performed in the same manner as in Example 1 except that Developers B to E were used instead of Developer A of Example 1.
(Comparative Example 1)
In Comparative Example 1, evaluation was performed in the same manner as in Example 1 except that Developer F was used instead of Developer A in Example 1.

スクイズローラ303通過後の現像剤の液量は3g/m2(固形分67%)であった。
(評価)
転写効率:転写後の中間転写体上のトナーを目視観察し、全く認められないものを○、わずかに認められるが問題とならないレベルのものを△、はっきりと確認でき、問題となるレベルのものを×とした。
The amount of the developer after passing through the squeeze roller 303 was 3 g / m 2 (solid content: 67%).
(Evaluation)
Transfer efficiency: Visual observation of the toner on the intermediate transfer member after transfer, ○ that is not recognized at all, △ that is slightly recognized but not causing a problem, that can be clearly confirmed, and that has a problem level Was marked with x.

定着性評価:定着画像のテープ剥離試験を行った。テープには、Scotchメンディングテープ(住友3M社製)を用いた。テープ剥離前後の反射濃度を測定し、前後の濃度比が90%以上のものを○、80%以上90%未満のものを△、80%未満のものを×とし、△以上を合格とした。(測定は、X−Rite社の濃度計使用)
評価結果を表1に示す。
Fixability evaluation: A tape peel test of a fixed image was performed. As the tape, a Scotch mending tape (manufactured by Sumitomo 3M) was used. The reflection density before and after the tape peeling was measured, and the density ratio before and after the tape was 90% or more, ○ was 80% or more and less than 90%, Δ was less than 80%, and Δ or more was passed. (Measurement uses X-Rite densitometer)
The evaluation results are shown in Table 1.

Figure 2009036814
Figure 2009036814

表1の結果から、比較例1に比べ実施例1〜5の定着強度が良くなっているのは、本発明に係る画像形成装置において、液体現像剤が、不揮発性液体であるキャリア液と、顔料微粒子と、熱可塑性の樹脂微粒子と、を含み、画像担持体上の液体現像剤の層のキャリア液を除去するキャリア液除去手段を有し、キャリア液除去手段により画像担持体上の液体現像剤の層のキャリア液を除去した後に、画像担持体上の液体現像剤の層を記録媒体に転写することによることが分かる。また、実施例1〜4に比べ、実施例5において、定着強度がやや低下しているのは、実施例5の顔料微粒子の粒径が1500nmと大きく、キャリア液除去手段におけるキャリア液の除去の効果が減少したためと考えられる。   From the results in Table 1, the fixing strengths of Examples 1 to 5 are improved compared to Comparative Example 1 in the image forming apparatus according to the present invention, in which the liquid developer is a non-volatile liquid carrier liquid, The liquid developer on the image carrier is provided with a carrier liquid removing means for removing the carrier liquid in the liquid developer layer on the image carrier, the pigment fine particles and the thermoplastic resin fine particles. It can be seen that the liquid developer layer on the image carrier is transferred to the recording medium after the carrier liquid in the agent layer is removed. Further, the fixing strength in Example 5 is slightly lower than in Examples 1 to 4, because the particle size of the pigment fine particles in Example 5 is as large as 1500 nm, and the carrier liquid is removed by the carrier liquid removing means. It is thought that the effect decreased.

本発明の実施形態における画像形成装置の全体構成を示す図である。1 is a diagram illustrating an overall configuration of an image forming apparatus according to an embodiment of the present invention. 本発明の別の実施形態における画像形成装置の全体構成を示す図である。It is a figure which shows the whole structure of the image forming apparatus in another embodiment of this invention. キャリア液の除去を行った画像担持体上のトナー像を示す模式図である。It is a schematic diagram showing a toner image on the image carrier from which the carrier liquid has been removed.

符号の説明Explanation of symbols

101 クリーニングブレード
102 現像剤槽
103 現像ローラ
104 液体現像剤
105 コロトロン帯電装置
201 感光体
202 感光体クリーニングブレード
203 帯電装置
204 露光装置
301 中間転写体
302 1次転写ローラ
303 スクイズローラ
304 クリーニングブレード
305、306 バックアップローラ
307 転写ローラ
308 テンションローラ
309 ハロゲンヒータ
310 冷却部材
P 記録媒体
DESCRIPTION OF SYMBOLS 101 Cleaning blade 102 Developer tank 103 Developing roller 104 Liquid developer 105 Corotron charging device 201 Photoconductor 202 Photoconductor cleaning blade 203 Charging device 204 Exposure device 301 Intermediate transfer body 302 Primary transfer roller 303 Squeeze roller 304 Cleaning blades 305 and 306 Backup roller 307 Transfer roller 308 Tension roller 309 Halogen heater 310 Cooling member P Recording medium

Claims (6)

液体現像剤を用いて現像した画像を記録媒体に転写する画像形成装置において、
不揮発性のキャリア液と、該キャリア液に分散された顔料微粒子と、該キャリア液に分散された熱可塑性の樹脂微粒子とを含む液体現像剤を用いて静電潜像を現像する現像手段と、
該現像手段で顕像化した画像を担持する画像担持体上の液体現像剤の層のキャリア液の一部を除去するキャリア液除去手段と、
該キャリア液除去手段でキャリア液の一部を除去した後の前記画像担持体上の画像を記録媒体に転写する転写手段とを備えたことを特徴とする画像形成装置。
In an image forming apparatus for transferring an image developed using a liquid developer to a recording medium,
Developing means for developing an electrostatic latent image using a liquid developer comprising a non-volatile carrier liquid, pigment fine particles dispersed in the carrier liquid, and thermoplastic resin fine particles dispersed in the carrier liquid;
A carrier liquid removing means for removing a part of the carrier liquid in the layer of the liquid developer on the image carrier that carries the image visualized by the developing means;
An image forming apparatus comprising: transfer means for transferring an image on the image carrier after removing a part of the carrier liquid by the carrier liquid removing means to a recording medium.
前記樹脂微粒子は、前記キャリア液中における体積平均粒径が、10nm以上500nm以下であることを特徴とする請求項1に記載の画像形成装置。 The image forming apparatus according to claim 1, wherein the resin fine particles have a volume average particle diameter in the carrier liquid of 10 nm to 500 nm. 前記顔料微粒子は、前記キャリア液中における体積平均粒径が、30nm以上500nm以下であることを特徴とする請求項1又は2に記載の画像形成装置。 3. The image forming apparatus according to claim 1, wherein the pigment fine particles have a volume average particle diameter in the carrier liquid of 30 nm or more and 500 nm or less. 前記キャリア液除去手段は、前記画像担持体上の液体現像剤の層に接触し、前記顔料微粒子の帯電極性と同極性の電圧が印加された摺動体であることを特徴とする請求項1乃至3の何れか1項に記載の画像形成装置。 2. The carrier liquid removing unit according to claim 1, wherein the carrier liquid removing means is a sliding body that is in contact with a liquid developer layer on the image carrier and to which a voltage having the same polarity as the charged polarity of the pigment fine particles is applied. 4. The image forming apparatus according to any one of items 3. 前記転写手段は、ヒータを有する加熱ローラであることを特徴とする請求項1乃至4の何れか1項に記載の画像形成装置。 The image forming apparatus according to claim 1, wherein the transfer unit is a heating roller having a heater. 前記キャリア液除去手段で前記画像担持体上の液体現像剤の層のキャリア液を除去した後、前記転写手段で記録媒体に転写するまでの間で、前記画像担持体上の液体現像剤の層を加熱する加熱手段を有することを特徴とする請求項1乃至5の何れか1項に記載の画像形成装置。 After the carrier liquid in the liquid developer layer on the image carrier is removed by the carrier liquid removing unit, the liquid developer layer on the image carrier is transferred from the carrier liquid to the recording medium by the transfer unit. The image forming apparatus according to claim 1, further comprising a heating unit that heats the image forming apparatus.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2244130A3 (en) * 2009-04-22 2011-04-06 Seiko Epson Corporation Image forming apparatus and image forming method
JP2013105035A (en) * 2011-11-14 2013-05-30 Konica Minolta Business Technologies Inc Liquid developer

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JPH06138718A (en) * 1992-10-28 1994-05-20 Nippon Steel Chem Co Ltd Electrophotographic liquid developer
JP2000056575A (en) * 1998-08-05 2000-02-25 Pfu Ltd Wet type electrophotographic device
JP2001092199A (en) * 1999-09-22 2001-04-06 Toshiba Tec Corp Image forming device
JP2003175612A (en) * 2001-10-05 2003-06-24 Fuji Photo Film Co Ltd Recording head and recording apparatus

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Publication number Priority date Publication date Assignee Title
JPH06138718A (en) * 1992-10-28 1994-05-20 Nippon Steel Chem Co Ltd Electrophotographic liquid developer
JP2000056575A (en) * 1998-08-05 2000-02-25 Pfu Ltd Wet type electrophotographic device
JP2001092199A (en) * 1999-09-22 2001-04-06 Toshiba Tec Corp Image forming device
JP2003175612A (en) * 2001-10-05 2003-06-24 Fuji Photo Film Co Ltd Recording head and recording apparatus

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2244130A3 (en) * 2009-04-22 2011-04-06 Seiko Epson Corporation Image forming apparatus and image forming method
JP2013105035A (en) * 2011-11-14 2013-05-30 Konica Minolta Business Technologies Inc Liquid developer

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