JPH05204192A - Electrophotographic liquid developer and its production - Google Patents

Electrophotographic liquid developer and its production

Info

Publication number
JPH05204192A
JPH05204192A JP4063556A JP6355692A JPH05204192A JP H05204192 A JPH05204192 A JP H05204192A JP 4063556 A JP4063556 A JP 4063556A JP 6355692 A JP6355692 A JP 6355692A JP H05204192 A JPH05204192 A JP H05204192A
Authority
JP
Japan
Prior art keywords
rosin
ethylene
liquid developer
pigment
toner
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
JP4063556A
Other languages
Japanese (ja)
Inventor
Shoichi Shinozuka
塚 正 一 篠
Yoshiyuki Ozawa
澤 善 行 小
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.)
Seiko Epson Corp
Original Assignee
Seiko Epson Corp
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 Seiko Epson Corp filed Critical Seiko Epson Corp
Priority to JP4063556A priority Critical patent/JPH05204192A/en
Publication of JPH05204192A publication Critical patent/JPH05204192A/en
Pending legal-status Critical Current

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  • Liquid Developers In Electrophotography (AREA)

Abstract

PURPOSE:To obtain a clear toner image having enough density by using a developer containing a high-insulating carrier liquid having low dielectric constant and a toner dispersed in the carrier, the toner essentially comprising ethylene copolymers and a pigment coated with rosin or its deriv. CONSTITUTION:Toner particles essentially comprising a colorant and a resin to fix and impart charges to the toner particles are dispersed in a high-insulating carrier liquid having low dielectric constant. The colorant of the toner particle is a pigment coated with rosin or its deriv. The resin in the toner is ethylene copolymers. Both of the rosin or its deriv. which covers pigment particles and the ethylene copolymer form such a structure that the ethylene copolymer is adsorbed or deposited on the rosin or its deriv. The ethylene copolymer is preferably ethylene-vinyl acetate copolymers and/or ethylene acrylate copolymers having >=10 melt index and >=10wt.% polar group content.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[発明の背景][Background of the Invention]

【産業上の利用分野】本発明は、電子写真方式の湿式現
像法を用いた複写機、プリンタなどの記録装置に用いら
れる現像剤に関し、特に中間転写方式の記録装置におい
て、小さな圧力によって記録紙上に充分な濃度および明
瞭な輪郭のトナー像を与える現像剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a developer used in a recording apparatus such as a copying machine and a printer which uses an electrophotographic wet developing method, and particularly, in an intermediate transfer recording apparatus, a small pressure is applied to a recording paper. To a developer that provides a toner image with sufficient density and a clear contour.

【0002】[0002]

【従来の技術】従来、電子写真用液体現像剤としては、
スチレン樹脂、アクリル樹脂等の熱可塑性樹脂とカーボ
ンブラックのような顔料または染料からなる着色剤とを
主成分とするトナーを、石油系脂肪族炭化水素溶媒から
なる担体液中に分散したものが知られている(例えば特
開昭55−35321号)。さらに、より高い解像度を
得るために、加熱時に無極性溶媒に相溶するエチレン共
重合樹脂を用いたもの(米国特許4794651号、4
842974号、特開昭61−189248号)が提案
されている。
2. Description of the Related Art Conventionally, as a liquid developer for electrophotography,
It is known that a toner mainly composed of a thermoplastic resin such as styrene resin or acrylic resin and a colorant composed of a pigment or dye such as carbon black is dispersed in a carrier liquid composed of a petroleum-based aliphatic hydrocarbon solvent. (For example, JP-A-55-35321). Furthermore, in order to obtain higher resolution, an ethylene copolymer resin compatible with a nonpolar solvent when heated is used (US Pat. No. 4,794,651, 4).
No. 842974 and JP-A-61-189248) have been proposed.

【0003】しかしながら前述したような液体現像剤
は、顔料への樹脂や荷電制御剤の吸着にばらつきがあ
り、現像特性を安定させにくい場合があった。また、と
くにカーボンブラックは他の多くの有機顔料と異なり導
電性を有することから、フルカラー記録の場合、黒と他
の色とに現像特性の差が生じてその調整が困難であっ
た。
However, in the liquid developer as described above, there are variations in the adsorption of the resin and the charge control agent to the pigment, and it may be difficult to stabilize the developing characteristics. In addition, carbon black, in particular, has conductivity unlike many other organic pigments. Therefore, in the case of full-color recording, there is a difference in development characteristics between black and other colors, which makes adjustment difficult.

【0004】さらに、このような液体現像剤を用い中間
転写方式の記録装置によって記録を行うと、転写効率が
悪く記録紙上に充分な濃度の像が得られず、また輪郭の
明瞭な像が得られないという問題点を有していた。ここ
で、中間転写方式とは、感光体上に静電潜像を形成し、
これを液体現像剤で現像し、この像を中間転写ベルト又
はドラムに転写し、そしてこのトナー像をさらに記録紙
に転写する方法である(例えば米国特許4708460
号公報参照)。この中間転写方式においては、トナー像
の中間転写ベルトから記録紙への転写を、両者の間に圧
力を印加しながら行っており、トナー像を記録紙に充分
付着させるためにはこの圧力を大きくする必要がある。
しかしながら、実際の装置において付与できる圧力には
限界があり、充分な付着力が得られず、したがって転写
効率が低くなってしまっていた。
Further, when recording is performed by an intermediate transfer type recording apparatus using such a liquid developer, the transfer efficiency is poor and an image having a sufficient density cannot be obtained on the recording paper, and an image with a clear outline is obtained. It had a problem that it could not be done. Here, the intermediate transfer method forms an electrostatic latent image on a photoconductor,
This is developed with a liquid developer, this image is transferred to an intermediate transfer belt or drum, and this toner image is further transferred to a recording paper (for example, US Pat. No. 4,708,460).
(See the official gazette). In this intermediate transfer system, the toner image is transferred from the intermediate transfer belt to the recording paper while applying a pressure between them, and this pressure is increased in order to sufficiently adhere the toner image to the recording paper. There is a need to.
However, there is a limit to the pressure that can be applied in an actual device, a sufficient adhesive force cannot be obtained, and thus the transfer efficiency is reduced.

【0005】[発明の概要][Outline of the Invention]

【発明が解決しようとする課題】従って本発明は、電子
写真方式の湿式現像法を用いた複写機、プリンタなどの
記録装置に用いられる優れた特性の現像剤およびその製
造法を提供することを目的としている。
SUMMARY OF THE INVENTION Therefore, the present invention provides a developer having excellent characteristics used in a recording apparatus such as a copying machine or a printer, which uses an electrophotographic wet developing method, and a method for producing the same. Has a purpose.

【0006】更に本発明は、中間転写方式の記録装置に
おいて、小さな圧力によって記録紙上に充分な濃度およ
び明瞭な輪郭のトナー像を与える現像剤およびその製造
法を提供することを目的としている。
A further object of the present invention is to provide a developer which gives a toner image having sufficient density and a clear contour on a recording paper by a small pressure in an intermediate transfer type recording apparatus, and a method for producing the same.

【0007】[0007]

【課題を解決するための手段】本発明による電子写真用
液体現像剤は、(a) 高絶縁性低誘電率担体液と、(b)該
担体液に分散されている、ロジンまたはその誘導体で被
覆された顔料とエチレン共重合体とを主成分としてなる
トナーとを含んでなるもの,である。
The liquid developer for electrophotography according to the present invention comprises (a) a highly insulating low dielectric constant carrier liquid and (b) a rosin or a derivative thereof dispersed in the carrier liquid. And a toner containing a coated pigment and an ethylene copolymer as a main component.

【0008】また、本発明の電子写真用液体現像剤の製
造法は、高絶縁性低誘電率担体液にエチレン共重合体を
加えて加熱溶解し、更にロジンまたはその誘導体で被覆
された顔料を加え、その後分散することを特徴とするも
の、である。
Further, in the method for producing a liquid developer for electrophotography of the present invention, an ethylene copolymer is added to a highly insulating low dielectric constant carrier liquid and dissolved by heating, and a pigment coated with rosin or its derivative is further added. In addition, it is characterized by being dispersed thereafter.

【0009】[発明の具体的説明]本発明による液体現
像剤は、(i) 着色剤と(ii)固着のためおよびトナー粒子
に電荷を付与のための樹脂とを主成分とするトナー粒子
を、高絶縁性低誘電率担体液(以下では単に「担体液」
という場合がある)に分散させたものである。本発明に
よる液体現像剤のトナー粒子は、着色剤としてロジンま
たはその誘導体で被覆された顔料を、樹脂としてエチレ
ン共重合体を用いたものである。
DETAILED DESCRIPTION OF THE INVENTION The liquid developer according to the present invention comprises toner particles containing (i) a colorant and (ii) a resin for fixing and for imparting an electric charge to the toner particles as main components. , High insulating low dielectric constant carrier liquid (hereinafter referred to simply as "carrier liquid"
It may be said that it is dispersed. The toner particles of the liquid developer according to the present invention use a pigment coated with rosin or its derivative as a colorant and an ethylene copolymer as a resin.

【0010】本発明において、顔料表面を被覆している
ロジンまたはその誘導体とエチレン共重合体の両者は、
ロジンまたはその誘導体表面にエチレン共重合体が吸着
および/または付着した構造をとる。ここで、吸着およ
び/または付着とは、ロジンまたはその誘導体とエチレ
ン共重合体とが、微視的に見た場合水素結合などを介し
て物理的に結合している状態をいい、巨視的に見た場合
ロジンまたはその誘導体表面をエチレン共重合体の樹脂
が被覆しているような状態をいう。さらに、巨視的に見
た場合のロジンまたはその誘導体とエチレン共重合体と
の界面は均一である必要はなく、互いに混じり合った相
溶部分を有していてもよく、またそのような相溶部分を
有することが本発明にあっては有利である。
In the present invention, both the rosin or its derivative coating the surface of the pigment and the ethylene copolymer are
It has a structure in which an ethylene copolymer is adsorbed and / or attached to the surface of rosin or its derivative. Here, the adsorption and / or adhesion means a state in which the rosin or its derivative and the ethylene copolymer are physically bound via a hydrogen bond or the like when viewed microscopically, and macroscopically. When viewed, it means that the surface of rosin or its derivative is covered with an ethylene copolymer resin. Furthermore, the interface between the rosin or its derivative and the ethylene copolymer when viewed macroscopically does not need to be uniform, and may have compatible parts mixed with each other, and Having a portion is advantageous in the present invention.

【0011】前記のようなトナー粒子構造を実現するた
めには、ロジンまたはその誘導体に対し難溶もしくは微
溶程度の溶解性を有しかつエチレン共重合体に対し加熱
溶解時相溶する性質を有する担体液を選択することがま
ず必要であり、また、ロジンまたはその誘導体とエチレ
ン共重合体とは常温で完全相溶するような組合せを選択
する必要がある。
In order to realize the toner particle structure as described above, it is necessary to have a property that it is hardly soluble or slightly soluble in rosin or its derivative and is compatible with the ethylene copolymer upon heating and dissolution. First, it is necessary to select a carrier liquid having the same, and it is necessary to select a combination in which the rosin or its derivative and the ethylene copolymer are completely compatible at room temperature.

【0012】本発明においてロジンとはアビエチン酸を
主成分とした樹脂をいい、またその誘導体とはロジンを
水素添加、エステル化、重合等したものをいう。誘導体
の具体例としてはガムロジン、ウッドロジン、ロジング
リセリンエステル、ロジンペンタエリスリトールエステ
ル、部分水素添加ロジン、完全水素添加ロジン、部分水
素添加ロジンメチルエステル、部分水素添加ロジントリ
エチレングリコールエステル、部分水素添加ロジングリ
セリンエステル、部分水素添加ロジンペンタエリスリト
ールエステル、完全水素添加ロジングリセリンエステ
ル、完全水素添加ロジンペンタエリスリトールエステ
ル、ロジンアルコール、マレイン酸変性ロジン、マレイ
ン酸変性ロジンエステル、ロジン変性フェノール、重合
ロジン、重合ロジンエステル等が挙げられる。
In the present invention, the rosin means a resin containing abietic acid as a main component, and the derivative thereof means a resin obtained by hydrogenating, esterifying or polymerizing rosin. Specific examples of the derivative include gum rosin, wood rosin, rosin glycerin ester, rosin pentaerythritol ester, partially hydrogenated rosin, fully hydrogenated rosin, partially hydrogenated rosin methyl ester, partially hydrogenated rosin triethylene glycol ester, partially hydrogenated rosin glycerin. Ester, partially hydrogenated rosin pentaerythritol ester, fully hydrogenated rosin glycerin ester, fully hydrogenated rosin pentaerythritol ester, rosin alcohol, maleic acid modified rosin, maleic acid modified rosin ester, rosin modified phenol, polymerized rosin, polymerized rosin ester, etc. Is mentioned.

【0013】ロジンまたはその誘導体で被覆された顔料
は、ロジンまたはその誘導体を良く溶解するケトン、エ
ステル、トルエン等の溶剤に溶解して、所望の顔料を加
えてアトライター、ボールミル等の分散機で分散した
後、溶剤を留除することによって製造することができ
る。さらには、フラッシング分散法によっても製造する
ことができる。また、顔料とロジンまたはその誘導体の
重量比は1:0.1〜1:1が好ましい。より好ましく
は1:0.2〜1:0.5である。
The pigment coated with rosin or its derivative is dissolved in a solvent such as ketone, ester or toluene which dissolves rosin or its derivative well, and the desired pigment is added to the pigment with a disperser such as an attritor or a ball mill. After the dispersion, it can be produced by distilling off the solvent. Further, it can be manufactured by the flushing dispersion method. The weight ratio of pigment to rosin or its derivative is preferably 1: 0.1 to 1: 1. It is more preferably 1: 0.2 to 1: 0.5.

【0014】またロジンエステルで被覆された市販の加
工顔料を用いることも可能であり、その具体例として
は、マイクロリスイエロー2G−T、マイクロリスイエ
ロー3R−T、マイクロリスブラウン5R−T、マイク
ロリススカーレットR−T、マイクロリスレッドBR−
T、マイクロリスブルーGS−T、マイクロリスブルー
4G−T、マイクロリスグリーンG−T、マイクロリス
ブラックC−T(以上、チバガイギー社製)などがあげ
られる。
It is also possible to use a commercially available processed pigment coated with rosin ester, and specific examples thereof include Microlith Yellow 2G-T, Microlith Yellow 3R-T, Microlith Brown 5R-T and Microlith Brown. Squirrel Scarlet R-T, Micro Res red BR-
T, Microlith Blue GS-T, Microlith Blue 4G-T, Microlith Green GT, Microlith Black CT (above, manufactured by Ciba Geigy) and the like.

【0015】本発明の好ましい態様によれば、エチレン
共重合体としては、エチレンビニルアセテート共重合樹
脂、エチレンエチルアクリレート共重合樹脂などがあげ
られる。特に、メルトインデックス(MI)が10以上
で極性基含有量が10重量%以上であるものが好まし
い。MIが10未満であると、トナー粒子の分散安定性
に欠ける場合があり好ましくない。また、極性基含有量
が10重量%未満であるとトナー粒子としての電荷量が
十分でなくなる場合があり、好ましくない。MIが10
以上で極性基含有量が10重量%以上であるエチレンビ
ニルアセテート共重合体の具体例としては、NUC−3
140、NUC−3140BK、NUC−3145、N
UC−3460、DQDJ−3868、NUC−315
0、NUC−3160、NUC−3190、DQDJ−
3269、NUC−3165、NUC−3170、DQ
DJ−7179、NUC−3185、MB−010、M
B−030、MB−600、MB−850、MB−99
0、MB−080(以上、日本ユニカー社製)、EV4
5X、EV40、EV40X、V577−2、EV−1
50、V523、EV−210、V541、EV22
0、V542、EV220NC、EV250、EV25
0SS、EV250C、EV310、V577、EV4
10、EV420、EV450、EV550、P140
7C、P1207、P1207C、EV640(以上、
三井デュポンポリケミカル社製)などがあげられる。
According to a preferred embodiment of the present invention, examples of the ethylene copolymer include ethylene vinyl acetate copolymer resin and ethylene ethyl acrylate copolymer resin. Particularly, those having a melt index (MI) of 10 or more and a polar group content of 10% by weight or more are preferable. When the MI is less than 10, the dispersion stability of the toner particles may be insufficient, which is not preferable. If the polar group content is less than 10% by weight, the charge amount of the toner particles may become insufficient, which is not preferable. MI is 10
Specific examples of the ethylene vinyl acetate copolymer having a polar group content of 10% by weight or more include NUC-3.
140, NUC-3140BK, NUC-3145, N
UC-3460, DQDJ-3868, NUC-315
0, NUC-3160, NUC-3190, DQDJ-
3269, NUC-3165, NUC-3170, DQ
DJ-7179, NUC-3185, MB-010, M
B-030, MB-600, MB-850, MB-99
0, MB-080 (above, made by Nippon Unicar), EV4
5X, EV40, EV40X, V577-2, EV-1
50, V523, EV-210, V541, EV22
0, V542, EV220NC, EV250, EV25
0SS, EV250C, EV310, V577, EV4
10, EV420, EV450, EV550, P140
7C, P1207, P1207C, EV640 (above,
Mitsui DuPont Polychemical Co., Ltd.) and the like.

【0016】また、MIが10以上で極性基含有量が1
0重量%以上であるエチレンエチルアクリレート共重合
樹脂としては、DPDJ−9169、NUC−607
0、MB−730、MB−870、MB−900、MB
−910(以上、日本ユニカー社製)、A−704、A
−706、A−707、A−709(以上、三井デュポ
ンポリケミカル社製)などがあげられる。
Further, MI is 10 or more and the polar group content is 1
The ethylene ethyl acrylate copolymer resin of 0% by weight or more includes DPDJ-9169 and NUC-607.
0, MB-730, MB-870, MB-900, MB
-910 (above, manufactured by Nippon Unicar Co., Ltd.), A-704, A
-706, A-707, A-709 (above, Mitsui DuPont Polychemical Co., Ltd. make) etc. are mentioned.

【0017】高絶縁性低誘電率担体液については、前記
のようなロジンまたはその誘導体で被覆した顔料および
エチレン共重合体を用いる限り、従来の電子写真用液体
現像剤に用いられているものをそのまま用いることがで
きる。例えば、1013Ω・cm以上の高絶縁性と、3以下
の低誘電率を有する担体液が好ましく用いられる。具体
的には、脂肪族炭化水素系の溶媒であるエクソール、ア
イソパー(以下、エクソン化学社製)、IPソルベント
(出光石油化学社製)、シェルゾル(シェル化学社製)
等が好ましく用いられる。
As the high insulating low dielectric constant carrier liquid, as long as the pigment and the ethylene copolymer coated with the rosin or its derivative as described above are used, those used in conventional liquid developers for electrophotography are used. It can be used as it is. For example, a carrier liquid having a high insulating property of 10 13 Ω · cm or more and a low dielectric constant of 3 or less is preferably used. Specifically, aliphatic hydrocarbon solvents such as Exsol, Isopar (hereinafter Exxon Chemical Co., Ltd.), IP Solvent (Idemitsu Petrochemical Co., Ltd.), Shell Sol (Shell Chemical Co., Ltd.)
Etc. are preferably used.

【0018】また、現像剤の諸特性を改善するために第
三成分として、電荷制御剤等の添加剤も必要に応じて使
用できる。
If necessary, additives such as a charge control agent can be used as a third component in order to improve various properties of the developer.

【0019】本発明による液体現像剤は次のようにして
製造することができる。まず、前記した高絶縁性低誘電
率担体液にエチレン共重合体を加え加熱溶融する。この
溶解液に前記のロジンまたはその誘導体で被覆された顔
料をさらに加え、混合する。このロジンまたはその誘導
体で被覆された顔料の添加は、担体液とエチレン共重合
体の加熱溶液を加熱したままでもしくは冷却後のいずれ
であってもよいが、冷却後の添加が好ましい。エチレン
共重合体とロジンまたはその誘導体で被覆された顔料の
添加比は、顔料1重量部に対して好ましくは0.01〜
10重量部、より好ましくは0.1〜4重量部程度であ
る。また加熱溶解温度は、エチレン共重合体樹脂を担体
液に均一に溶解できる温度であれば良いが、具体的には
80〜200℃程度が好ましく、より好ましくは100
〜170℃程度である。ロジンまたはその誘導体で被覆
された顔料の添加された混合物を、適当な方法によって
攪拌すると、均一なゲル化された濃縮液を得る事ができ
る。この濃縮液を常法の分散手段、例えばボールミル、
アトライター、ビーズミルなどで分散することによって
所望の粒子径のトナー粒子とする。トナー粒子の大きさ
は、その使用条件に照らして適宜決定できるが、好まし
くは0.1〜5μm程度である。分散の後に、さらに担
体液によって希釈して適当な濃度とすれば現像剤として
用いる事ができる。なお、用いる分散方法に適切な粘度
領域がある場合には、分散工程前に担体液で希釈しても
良い。
The liquid developer according to the present invention can be manufactured as follows. First, an ethylene copolymer is added to the above-described high-insulating low-dielectric-constant carrier liquid and heated and melted. The pigment coated with the rosin or its derivative is further added to this solution and mixed. The pigment coated with the rosin or its derivative may be added either while the heated solution of the carrier liquid and the ethylene copolymer is heated or after cooling, but the addition after cooling is preferable. The addition ratio of the pigment coated with the ethylene copolymer and the rosin or its derivative is preferably 0.01 to 1 part by weight of the pigment.
The amount is 10 parts by weight, more preferably about 0.1 to 4 parts by weight. The heating dissolution temperature may be a temperature at which the ethylene copolymer resin can be uniformly dissolved in the carrier liquid, but specifically, it is preferably about 80 to 200 ° C, more preferably 100.
It is about 170 ° C. The added mixture of pigments coated with rosin or its derivatives can be stirred by a suitable method to obtain a homogeneous gelled concentrate. This concentrated liquid is dispersed by a conventional method such as a ball mill,
Toner particles having a desired particle size are obtained by dispersing with an attritor, a bead mill, or the like. The size of the toner particles can be appropriately determined depending on the use conditions, but is preferably about 0.1 to 5 μm. After dispersion, it can be used as a developer by further diluting it with a carrier liquid to give an appropriate concentration. If the dispersion method used has an appropriate viscosity range, it may be diluted with a carrier liquid before the dispersion step.

【0020】本発明による現像剤は、従来の湿式現像法
を用いた電子写真方式の現像装置にそのまま適用でき
る。本発明による現像剤は、従来の現像剤に比較して優
れた転写効率を実現することができる。具体的には従来
最高でも約70%程度であった転写効率を約90%程度
まで高めることが可能となる。特に、本発明による現像
剤を前記した中間転写方式の記録装置に用いると、現像
剤の転写効率が高いことから、小さな圧力でも記録紙上
に充分な濃度で明瞭な輪郭のトナー像を形成でき有利で
ある。
The developer according to the present invention can be directly applied to an electrophotographic developing device using a conventional wet developing method. The developer according to the present invention can realize excellent transfer efficiency as compared with the conventional developers. Specifically, it is possible to increase the transfer efficiency, which was conventionally about 70% at the maximum, to about 90%. In particular, when the developer according to the present invention is used in the above-mentioned intermediate transfer type recording apparatus, since the transfer efficiency of the developer is high, it is possible to form a toner image having a clear contour with sufficient density on the recording paper even with a small pressure. Is.

【0021】[0021]

【実施例】本発明をさらに以下の実施例によって詳細に
説明するが、本発明はこれらの実施例に限定されるもの
ではない。実施例1 MB−870(日本ユニカー社製エチレンエチルアクリ
レート共重合樹脂、MI:20、極性基含有量:41
%)10gをアイソパーG(エクソン化学社製脂肪族炭
化水素系溶剤)100gに加え、環流攪拌器付き容器に
て150℃で加熱溶解した。冷却後、この溶液にマイク
ロリスブラックC−T(チバガイギー社製ロジンエステ
ル加工顔料)10gと、レシチン(荷電制御剤)0.2
gと、アイソパーG79.8gとを加え、この混合物を
アトライターにて5時間分散し、200gの濃縮液を得
た。さらに、800gのアイソパーGで希釈し、電子写
真用液体現像剤とした。比較例1 マイクロリスブラックC−Tのかわりにカーボンブラッ
ク#44(三菱化成工業社製)を用いたほかは実施例1
と同様にして電子写真用液体現像剤を得た。
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples. Example 1 MB-870 (Ethylene ethyl acrylate copolymer resin manufactured by Nippon Unicar Co., Ltd., MI: 20, polar group content: 41)
%) 10 g was added to 100 g Isopar G (aliphatic hydrocarbon solvent manufactured by Exxon Chemical Co., Ltd.) and heated and dissolved at 150 ° C. in a vessel equipped with a reflux stirrer. After cooling, 10 g of Microlith Black CT (a rosin ester-processed pigment manufactured by Ciba Geigy) and lecithin (charge control agent) 0.2 were added to the solution.
g and 79.8 g of Isopar G were added, and this mixture was dispersed in an attritor for 5 hours to obtain 200 g of a concentrated liquid. Further, it was diluted with 800 g of Isopar G to obtain a liquid developer for electrophotography. Comparative Example 1 Example 1 except that carbon black # 44 (manufactured by Mitsubishi Kasei Co., Ltd.) was used instead of Microlith Black CT.
A liquid developer for electrophotography was obtained in the same manner as in.

【0022】実施例2 EV−410(三井デュポンポリケミカル社製エチレン
ビニルアセテート共重合樹脂、MI:400、極性基含
有量:19%)5gをIPソルベント1620(出光石
油化学社製脂肪族炭化水素系溶剤)100gに加え、環
流攪拌器付き容器にて150℃で加熱溶解した、冷却
後、この溶液にマイクロリスイエロー2G−T(チバガ
イギー社製ロジンエステル加工顔料)15gと、レシチ
ン(荷電制御剤)0.3gと、IPソルベント1620
79.7gとを加え、この混合物をアトライターにて4
時間分散し、200gの濃縮液を得た。さらに、800
gのIPソルベント1620で希釈し、電子写真用液体
現像剤とした。比較例2 マイクロリスイエロー2G−Tのかわりにベンジジンイ
エローを用いたほかは実施例2と同様にして電子写真用
液体現像剤を得た。
Example 2 5 g of EV-410 (ethylene vinyl acetate copolymer resin manufactured by Mitsui DuPont Polychemical Co., MI: 400, polar group content: 19%) was added to IP Solvent 1620 (aliphatic hydrocarbon manufactured by Idemitsu Petrochemical Co., Ltd.). System solvent) 100 g, and heated and dissolved at 150 ° C. in a vessel equipped with a reflux stirrer, and after cooling, 15 g of Microlith Yellow 2G-T (rosin ester processed pigment manufactured by Ciba Geigy) and lecithin (charge control agent) ) 0.3 g and IP Solvent 1620
79.7 g was added, and this mixture was mixed with an attritor 4
After time-dispersion, 200 g of concentrated liquid was obtained. In addition, 800
It was diluted with 1 g of IP solvent 1620 to obtain a liquid developer for electrophotography. Comparative Example 2 A liquid developer for electrophotography was obtained in the same manner as in Example 2 except that Benzidine Yellow was used instead of Microlith Yellow 2G-T.

【0023】実施例3 EV−450(三井デュポンポリケミカル社製エチレン
ビニルアセテート共重合樹脂、MI:15、極性基含有
量:19%)5g及びMB−900(日本ユニカー社製
エチレンエチルアクリレート共重合樹脂、MI:150
0、極性基含有量;23%)15gをシェルゾル70L
(シェル化学社製脂肪族炭化水素系溶剤)100gに加
え、環流攪拌器付き容器にて150℃で加熱溶解した。
冷却後、この溶液にマイクロリスレッドBR−T(チバ
ガイギー社製ロジンエステル加工顔料)7gと、レシチ
ン(荷電制御剤)0.14gと、シェルゾル70L 7
2.86gとを加え、この混合物をアトライターで4時
間分散し、200gの濃縮液を得た。さらに、800g
のシェルゾル70Lで希釈し、電子写真用液体現像剤と
した。比較例3 マイクロリスレッドBR−Tのかわりにブリリアントカ
ーミン6Bを用いたほかは実施例3と同様にして電子写
真用液体現像剤を得た。
Example 3 5 g of EV-450 (ethylene vinyl acetate copolymer resin manufactured by Mitsui DuPont Polychemical, MI: 15, polar group content: 19%) and MB-900 (ethylene ethyl acrylate copolymer manufactured by Nippon Unicar Co., Ltd.) Resin, MI: 150
0, polar group content; 23%) 15g shell sol 70L
(Aliphatic hydrocarbon solvent manufactured by Shell Chemical Co.) was added to 100 g, and the mixture was heated and dissolved at 150 ° C. in a vessel equipped with a reflux stirrer.
After cooling, 7 g of Microresid BR-T (a rosin ester-processed pigment manufactured by Ciba Geigy), 0.14 g of lecithin (charge control agent), and Shell Sol 70L 7 were added to this solution.
2.86 g was added and the mixture was dispersed with an attritor for 4 hours to obtain 200 g of a concentrated liquid. In addition, 800g
Was diluted with 70 L of shell sol to prepare a liquid developer for electrophotography. Comparative Example 3 A liquid developer for electrophotography was obtained in the same manner as in Example 3 except that Brilliant Carmine 6B was used in place of Microresid BR-T.

【0024】実施例4 A−709(三井デュポンポリケミカル社製エチレンエ
チルアクリレート共重合樹脂、MI:25、極性基含有
量:35%)10gをアイソパーH(エクソン化学社製
脂肪族炭化水素系溶剤)100gに加え、環流攪拌器付
き容器にて150℃で加熱溶解した。冷却後、この溶液
にマイクロリスブルー4G−T(チバガイギー社製ロジ
ンエステル加工顔料)10gと、レシチン0.2gと、
アイソパーH79.8gとを加え、この混合物をアトラ
イターで4時間分散し、200gの濃縮液を得た。さら
に、800gのアイソパーHで希釈し、電子写真用液体
現像剤とした。比較例4 A−709のかわりにA−701(三井デュポンポリケ
ミカル社製エチレンエチルアクリレート共重合樹脂、M
I:5、極性基含有量:9%)を用いたほかは実施例4
と同様にして電子写真用液体現像剤を得た。
Example 4 10 g of A-709 (ethylene ethyl acrylate copolymer resin manufactured by Mitsui DuPont Polychemical Co., MI: 25, polar group content: 35%) was replaced with Isopar H (aliphatic hydrocarbon solvent manufactured by Exxon Chemical Co.). ) 100 g, and heated and dissolved at 150 ° C. in a vessel equipped with a reflux stirrer. After cooling, 10 g of Microlith Blue 4G-T (a rosin ester-processed pigment manufactured by Ciba Geigy) and 0.2 g of lecithin were added to this solution.
79.8 g of Isopar H was added, and this mixture was dispersed for 4 hours with an attritor to obtain 200 g of a concentrated liquid. Further, it was diluted with 800 g of Isopar H to obtain a liquid developer for electrophotography. Comparative Example 4 Instead of A-709, A-701 (Mitsui DuPont Polychemical Co., Ltd. ethylene ethyl acrylate copolymer resin, M
Example 4 except that I: 5 and polar group content: 9%) were used.
A liquid developer for electrophotography was obtained in the same manner as in.

【0025】実施例5 NUC−3185(日本ユニカー社製エチレンビニルア
セテート共重合樹脂、MI:400、極性基含有量:2
8%)3gをアイソパーG(エクソン化学社製脂肪族炭
化水素系溶剤)100gに加え、環流攪拌器付き容器に
て150℃で加熱溶解した。冷却後、この溶液に、KE
T YELLOW 402(大日本インク化学工業社製
C.I.PIGMENT YELLOW 154)をス
テベライトエステル7(理化ハーキュレス社製部分水素
添加ロジングリセリンエステル)で被覆(重量比1:
0.3)したもの10gと、サンセパラ100(三洋化
成工業社製ジオクチルスルホコハク酸ナトリウム)0.
2gと、アイソパーG86.8gとを加え、この混合物
をアイガー・モーターミル(EIGER ENGINE
ERING LIMITED製ビーズミル)で20分間
分散し、200gの濃縮液を得た。さらに、800gの
アイソパーGで希釈し、電子写真用液体現像剤とした。比較例5 ステベライトエステル7で被覆した顔料のかわりに被覆
処理をしないKETYELLOW 402(大日本イン
ク化学工業社製C.I.PIGMENT YELLOW
154)を用いたほかは実施例5と同様にして電子写
真用液体現像剤を得た。
Example 5 NUC-3185 (Ethylene vinyl acetate copolymer resin manufactured by Nippon Unicar Co., MI: 400, polar group content: 2)
8%) (3 g) was added to 100 g of Isopar G (aliphatic hydrocarbon solvent manufactured by Exxon Chemical Co., Ltd.) and heated and dissolved at 150 ° C. in a vessel equipped with a reflux stirrer. After cooling, add KE to this solution.
T YELLOW 402 (CI PIGMENT YELLOW 154 manufactured by Dainippon Ink and Chemicals, Inc.) was coated with steberite ester 7 (partially hydrogenated rosin glycerin ester manufactured by Rika Hercules Co., Ltd. (weight ratio 1 :).
0.3) and Sansepara 100 (manufactured by Sanyo Chemical Industries, Ltd. sodium dioctyl sulfosuccinate).
2g and Isopar G86.8g were added, and this mixture was mixed with Eiger ENGINE.
It was dispersed for 20 minutes with an ERING LIMITED bead mill) to obtain 200 g of a concentrated liquid. Further, it was diluted with 800 g of Isopar G to obtain a liquid developer for electrophotography. Comparative Example 5 KETYELLOW 402 (CI PIGMENT YELLOW manufactured by Dainippon Ink and Chemicals, Inc.) was used without coating treatment in place of the pigment coated with steberite ester 7.
A liquid developer for electrophotography was obtained in the same manner as in Example 5 except that 154) was used.

【0026】実施例6 MB−910(日本ユニカー社製エチレンエチルアクリ
レート共重合樹脂、MI:1100、極性基含有量:2
8%)5gをアイソパーG(エクソン化学社製脂肪族炭
化水素系溶剤)100gに加え、環流攪拌器付き容器に
て120℃で加熱溶解した。冷却後、この溶液に、KE
T RED 308(大日本インク化学工業社製C.
I.PIGMENT RED 31)をペンタリンA−
JA(理化ハーキュレス社製ロジンペンタエリスリトー
ルエステル)で被覆(重量比1:0.3)したもの10
gと、サンセパラ100(三洋化成工業社製ジオクチル
スルホコハク酸ナトリウム)0.2gと、アイソパーG
84.8gとを加え、この混合物をアイガー・モーター
ミル(EIGER ENGINEERING LIMI
TED製ビーズミル)で20分間分散し、200gの濃
縮液を得た。さらに、800gのアイソパーGで希釈
し、電子写真用液体現像剤とした。比較例6 ペンタリンA−JAで被覆した顔料のかわりに被覆処理
をしないKET RED308(大日本インク化学工業
社製C.I.PIGMENT RED 31)を用いた
ほかは実施例6と同様にして電子写真用液体現像剤を得
た。
Example 6 MB-910 (Ethylene ethyl acrylate copolymer resin manufactured by Nippon Unicar Co., Ltd., MI: 1100, polar group content: 2)
8%) (5 g) was added to 100 g of Isopar G (aliphatic hydrocarbon solvent manufactured by Exxon Chemical Co., Ltd.) and heated and dissolved at 120 ° C. in a vessel equipped with a reflux stirrer. After cooling, add KE to this solution.
T RED 308 (C. manufactured by Dainippon Ink and Chemicals, Inc.
I. PIGMENT RED 31) with pentaline A-
10 (weight ratio 1: 0.3) coated with JA (rosin pentaerythritol ester manufactured by Rika Hercules) 10
g, Sansepara 100 (Sanyo Chemical Co., Ltd. sodium dioctyl sulfosuccinate) 0.2 g, and Isopar G
84.8g and added to this mixture EIGER ENGINEERING LIMI
It was dispersed in a TED bead mill) for 20 minutes to obtain 200 g of a concentrated liquid. Further, it was diluted with 800 g of Isopar G to obtain a liquid developer for electrophotography. Comparative Example 6 Electrophotographic was performed in the same manner as in Example 6 except that KET RED 308 (CI PIGMENT RED 31 manufactured by Dainippon Ink and Chemicals, Inc.) was used instead of the pigment coated with pentaline A-JA. A liquid developer for use was obtained.

【0027】実施例7 MB−850(日本ユニカー社製エチレンビニルアセテ
ート共重合樹脂、MI:800、極性基含有量:22
%)2gをアイソパーG(エクソン化学社製脂肪族炭化
水素系溶剤)100gに加え、環流攪拌器付き容器にて
130℃で加熱溶解した。冷却後、この溶液に、KET
BLUE 118(大日本インク化学工業社製C.
I.PIGMENT BLUE 15)をペンタリン4
820(理化ハーキュレス社製マレイン酸変性ロジンエ
ステル)で被覆(重量比1:0.3)したもの10g
と、サンセパラ100(三洋化成工業社製ジオクチルス
ルホコハク酸ナトリウム)0.2gと、レシチン0.1
gと、アイソパーG87.7gとを加え、この混合物を
アイガー・モーターミル(EIGER ENGINEE
RING LIMITED製ビーズミル)で20分間分
散し、200gの濃縮液を得た。さらに、800gのア
イソパーGで希釈し、電子写真用液体現像剤とした。比較例7 ペンタリン4820で被覆した顔料のかわりに被覆処理
をしないKET BLUE 118(大日本インク化学
工業社製C.I.PIGMENT BLUE15)を用
いたほかは実施例7と同様にして電子写真用液体現像剤
を得た。
Example 7 MB-850 (ethylene vinyl acetate copolymer resin manufactured by Nippon Unicar Co., Ltd., MI: 800, polar group content: 22)
%) 2 g was added to 100 g of Isopar G (aliphatic hydrocarbon solvent manufactured by Exxon Chemical Co., Ltd.) and heated and dissolved at 130 ° C. in a vessel equipped with a reflux stirrer. After cooling, KET is added to this solution.
BLUE 118 (C. manufactured by Dainippon Ink and Chemicals, Inc.
I. PIGMENT BLUE 15) with pentaline 4
10 g coated with 820 (maleic acid modified rosin ester manufactured by Rika Hercules Co., Ltd.) (weight ratio 1: 0.3)
, Sansepara 100 (Sanyo Chemical Co., Ltd. sodium dioctyl sulfosuccinate) 0.2 g, and lecithin 0.1
g and Isopar G87.7 g were added, and the mixture was mixed with Eiger ENGINEE.
It was dispersed for 20 minutes with a RING LIMITED bead mill) to obtain 200 g of a concentrated liquid. Further, it was diluted with 800 g of Isopar G to obtain a liquid developer for electrophotography. Comparative Example 7 An electrophotographic liquid was prepared in the same manner as in Example 7, except that KET BLUE 118 (CI PIGMENT BLUE 15 manufactured by Dainippon Ink and Chemicals, Inc.) was used instead of the pigment coated with pentaline 4820. A developer is obtained.

【0028】実施例8 エバフレックスV577−2(三井デュポンポリケミカ
ル社製エチレンビニルアセテート共重合樹脂、MI:4
00、極性基含有量33%)7gをアイソパーG(エク
ソン化学社製脂肪族炭化水素系溶剤)100gに加え、
環流攪拌器付き容器にて120℃で加熱溶解した。冷却
後、この溶液にカーボンブラック#10B(三菱化成工
業社製)をタマノル135(荒川化学工業社製ロジン変
性フェノール)で被覆(重量比1:0.3)したもの1
0gと、サンセパラ100(三洋化成工業社製ジオクチ
ルスルホコハク酸ナトリウム)0.2gと、アイソパー
G82.8gとを加え、この混合物をアイガー・モータ
ーミル(EIGER ENGINEERING LIM
ITED製ビーズミル)で20分間分散し、200gの
濃縮液を得た。さらに、800gのアイソパーGで希釈
し、電子写真用液体現像剤とした。比較例8 タマノル135で被覆した顔料のかわりに被覆処理をし
ないカーボンブラック#10B(三菱化成工業社製)を
用いたほかは実施例8と同様にして電子写真用液体現像
剤を得た。
Example 8 Evaflex V577-2 (ethylene vinyl acetate copolymer resin manufactured by Mitsui DuPont Polychemical Co., MI: 4)
00, polar group content 33%) 7 g was added to 100 g Isopar G (aliphatic hydrocarbon solvent manufactured by Exxon Chemical Co.),
It melt | dissolved by heating at 120 degreeC in the container with a reflux mixer. After cooling, this solution was coated with carbon black # 10B (manufactured by Mitsubishi Kasei Kogyo Co., Ltd.) with Tamanol 135 (rosin modified phenol manufactured by Arakawa Chemical Industry Co., Ltd.) (weight ratio 1: 0.3) 1.
0 g, Sansepara 100 (Sanyo Chemical Co., Ltd. sodium dioctyl sulfosuccinate) 0.2 g, and Isopar G 82.8 g were added, and this mixture was mixed with an Eiger Motor Mill (EIGER ENGINEERING LIM).
It was dispersed in an ITED bead mill) for 20 minutes to obtain 200 g of a concentrated liquid. Further, it was diluted with 800 g of Isopar G to obtain a liquid developer for electrophotography. Comparative Example 8 A liquid developer for electrophotography was obtained in the same manner as in Example 8 except that uncoated carbon black # 10B (manufactured by Mitsubishi Kasei Co., Ltd.) was used in place of the pigment coated with Tamanor 135.

【0029】現像試験 実施例1〜8、比較例1〜8の電子写真用液体現像剤
を、特開平3−154085号、特開平2−26428
0号公報に記載の方法に基本的に従って、種々の記録紙
に記録した。
Development Tests The electrophotographic liquid developers of Examples 1 to 8 and Comparative Examples 1 to 8 were prepared according to the methods described in JP-A-3-154085 and JP-A-2-26428.
Recording was carried out on various recording papers basically according to the method described in JP-A-0.

【0030】第1図は、本発明の電子写真用液体現像剤
を用いた、中間転写方式の記録装置の断面図である。感
光体ドラム1の周囲に帯電装置2、露光装置3、現像装
置4、中間転写ドラム5、加圧ローラ6、剥離爪7、ク
リーニング装置8、除電装置10が順次配置されてい
る。中間転写ドラム5は、金属中空ドラム11とこれを
被覆する弾性層12により構成されている。弾性層12
としては、担体液の吸収性を有する事が望ましく、この
ような弾性層はシリコンゴムを用いることによって得る
ことができる。中間転写ドラム5には、転写残りトナー
を除去するクリーニング装置9が設けられている。
FIG. 1 is a cross-sectional view of an intermediate transfer type recording apparatus using the electrophotographic liquid developer of the present invention. A charging device 2, an exposure device 3, a developing device 4, an intermediate transfer drum 5, a pressure roller 6, a peeling claw 7, a cleaning device 8, and a charge eliminating device 10 are sequentially arranged around the photosensitive drum 1. The intermediate transfer drum 5 is composed of a hollow metal drum 11 and an elastic layer 12 covering the hollow metal drum 11. Elastic layer 12
It is preferable that the elastic layer has an absorbability of the carrier liquid, and such an elastic layer can be obtained by using silicon rubber. The intermediate transfer drum 5 is provided with a cleaning device 9 for removing transfer residual toner.

【0031】記録動作は以下のように行なわれる。帯電
工程、露光工程を経て感光体ドラム1上に静電潜像が形
成される。上記静電潜像は、現像装置4で液体現像剤を
用いて現像される。現像は帯電したトナーが電気泳動に
よって静電潜像に選択的に付着して行なわれ、感光体1
上にトナー像が形成される。次に中間転写ドラム5と感
光体ドラム1を当接させ電界を加えて、上記トナー像を
中間転写ドラム5に転写する。一方、給紙装置20より
搬出された、記録媒体である記録紙21は、中間転写ド
ラム5との当接位置まで搬送される。加圧ローラ6で圧
力を印加する。ここで中間転写ドラム5上のトナー像
が、記録紙21に付着し、転写される。トナー像を転写
した記録紙21は更に定着装置22に搬送され、熱圧力
定着され、排紙トレイ23に収納される。
The recording operation is performed as follows. An electrostatic latent image is formed on the photosensitive drum 1 through the charging process and the exposure process. The electrostatic latent image is developed by the developing device 4 using a liquid developer. The development is performed by electrifying the charged toner selectively on the electrostatic latent image, and
A toner image is formed on top. Next, the toner image is transferred to the intermediate transfer drum 5 by bringing the intermediate transfer drum 5 and the photosensitive drum 1 into contact with each other and applying an electric field. On the other hand, the recording paper 21, which is a recording medium, carried out from the paper feeding device 20 is conveyed to a contact position with the intermediate transfer drum 5. Pressure is applied by the pressure roller 6. Here, the toner image on the intermediate transfer drum 5 adheres to the recording paper 21 and is transferred. The recording paper 21 on which the toner image has been transferred is further conveyed to the fixing device 22, fixed under heat and pressure, and stored in the paper discharge tray 23.

【0032】前記記録方法により、一般上質紙、ボンド
紙、PPC用紙にビットイメージ記録、文字記録を行っ
たところ記録紙の種類によらず比較例に比較してさらに
良好な記録ができたことを確認した。さらに、マクベス
濃度計TR−927型で画像の反射濃度を測定した結果
を第1表に示す。
By the above recording method, bit image recording and character recording were performed on general high-quality paper, bond paper, and PPC paper, and it was found that better recording could be achieved compared to the comparative example regardless of the type of recording paper. confirmed. Further, Table 1 shows the results of measuring the reflection density of the image with a Macbeth densitometer TR-927 type.

【0033】 [0033]

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

【図1】本発明の電子写真用液体現像剤の記録に使用す
る記録装置の構成を示す断面図である。
FIG. 1 is a cross-sectional view showing a configuration of a recording apparatus used for recording an electrophotographic liquid developer of the present invention.

【符号の説明】[Explanation of symbols]

1 感光体ドラム 2 帯電装置 3 露光装置 4 現像装置 5 中間転写ドラム 6 加圧ローラ 7 剥離爪 8 クリーニング装置 9 クリーニング装置 10 除電装置 11 金属中空ドラム 12 弾性層 20 給紙装置 21 記録紙 22 定着装置 23 排紙トレイ 1 Photoreceptor Drum 2 Charging Device 3 Exposure Device 4 Developing Device 5 Intermediate Transfer Drum 6 Pressure Roller 7 Peeling Claw 8 Cleaning Device 9 Cleaning Device 10 Electrifying Device 11 Metal Hollow Drum 12 Elastic Layer 20 Paper Feeding Device 21 Recording Paper 22 Fixing Device 23 Output tray

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】(a) 高絶縁性低誘電率担体液と、 (b) 該担体液に分散されている、ロジンまたはその誘導
体で被覆された顔料とエチレン共重合体とを主成分とし
てなるトナーとを含んでなる、電子写真用液体現像剤。
1. A composition comprising (a) a highly insulating low dielectric constant carrier liquid, (b) a pigment coated with rosin or a derivative thereof and an ethylene copolymer dispersed in the carrier liquid. A liquid developer for electrophotography, comprising a toner.
【請求項2】前記エチレン共重合体が、メルトインデッ
クスが10以上でかつ極性基含有量が10重量%以上で
あるエチレンビニルアセテート共重合体および/または
エチレンエチルアクリレート共重合体である、請求項1
記載の電子写真用液体現像剤。
2. The ethylene copolymer is an ethylene vinyl acetate copolymer and / or an ethylene ethyl acrylate copolymer having a melt index of 10 or more and a polar group content of 10% by weight or more. 1
The described electrophotographic liquid developer.
【請求項3】高絶縁性低誘電率担体液にエチレン共重合
体を加えて加熱溶解し、更にロジンまたはその誘導体で
被覆された顔料を加え、その後分散することを特徴とす
る、電子写真用液体現像剤の製造法。
3. An electrophotographic apparatus, which comprises adding an ethylene copolymer to a highly insulating low dielectric constant carrier liquid, heating and dissolving the solution, further adding a pigment coated with rosin or a derivative thereof, and then dispersing the pigment. Liquid developer manufacturing method.
【請求項4】高絶縁性低誘電率担体液にエチレン共重合
体を加えて加熱溶解し、冷却した後にロジンまたはその
誘導体で被覆された顔料を加える、請求項3記載の電子
写真用液体現像剤の製造法。
4. The electrophotographic liquid developer according to claim 3, wherein an ethylene copolymer is added to a highly insulating low dielectric constant carrier liquid, the mixture is heated and dissolved, and after cooling, a pigment coated with rosin or a derivative thereof is added. Agent manufacturing method.
【請求項5】前記エチレン共重合体として、メルトイン
デックスが10以上でかつ極性基含有量が10重量%以
上であるエチレンビニルアセテート共重合体および/ま
たはエチレンエチルアクリレート共重合体を用いる、請
求項3または4記載の電子写真用液体現像剤の製造法。
5. An ethylene vinyl acetate copolymer and / or an ethylene ethyl acrylate copolymer having a melt index of 10 or more and a polar group content of 10% by weight or more is used as the ethylene copolymer. The method for producing a liquid developer for electrophotography according to 3 or 4.
【請求項6】前記顔料1重量部に対してエチレン共重合
体を0.1〜10重量部用いる、請求項3または4記載
の電子写真用液体現像剤の製造法。
6. The method for producing a liquid developer for electrophotography according to claim 3, wherein 0.1 to 10 parts by weight of an ethylene copolymer is used with respect to 1 part by weight of the pigment.
JP4063556A 1991-03-19 1992-03-19 Electrophotographic liquid developer and its production Pending JPH05204192A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4063556A JPH05204192A (en) 1991-03-19 1992-03-19 Electrophotographic liquid developer and its production

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP5457191 1991-03-19
JP3-312430 1991-11-27
JP31243091 1991-11-27
JP3-54571 1991-11-27
JP4063556A JPH05204192A (en) 1991-03-19 1992-03-19 Electrophotographic liquid developer and its production

Publications (1)

Publication Number Publication Date
JPH05204192A true JPH05204192A (en) 1993-08-13

Family

ID=27295333

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4063556A Pending JPH05204192A (en) 1991-03-19 1992-03-19 Electrophotographic liquid developer and its production

Country Status (1)

Country Link
JP (1) JPH05204192A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010025971A (en) * 2008-07-15 2010-02-04 Seiko Epson Corp Liquid developer and image forming apparatus
JP2010078691A (en) * 2008-09-24 2010-04-08 Seiko Epson Corp Liquid developer and image forming apparatus
JP2013125271A (en) * 2011-12-14 2013-06-24 Xerox Corp Toner with improved dielectric loss

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010025971A (en) * 2008-07-15 2010-02-04 Seiko Epson Corp Liquid developer and image forming apparatus
JP2010078691A (en) * 2008-09-24 2010-04-08 Seiko Epson Corp Liquid developer and image forming apparatus
JP2013125271A (en) * 2011-12-14 2013-06-24 Xerox Corp Toner with improved dielectric loss

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