JPH05333607A - Electrostatic charge developing liquid developer - Google Patents

Electrostatic charge developing liquid developer

Info

Publication number
JPH05333607A
JPH05333607A JP4164345A JP16434592A JPH05333607A JP H05333607 A JPH05333607 A JP H05333607A JP 4164345 A JP4164345 A JP 4164345A JP 16434592 A JP16434592 A JP 16434592A JP H05333607 A JPH05333607 A JP H05333607A
Authority
JP
Japan
Prior art keywords
pigment
toner particles
liquid developer
electrostatic charge
developer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP4164345A
Other languages
Japanese (ja)
Other versions
JP3248243B2 (en
Inventor
Akira Arikawa
晶 有川
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.)
Toyo Ink Mfg Co Ltd
Original Assignee
Toyo Ink Mfg Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyo Ink Mfg Co Ltd filed Critical Toyo Ink Mfg Co Ltd
Priority to JP16434592A priority Critical patent/JP3248243B2/en
Publication of JPH05333607A publication Critical patent/JPH05333607A/en
Application granted granted Critical
Publication of JP3248243B2 publication Critical patent/JP3248243B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To improve dispersion stability of toner particles and stability of chargeable polarity at the same time by using the liquid developer comprising the toner particles containing a pigment dispersed into a resin in the presence of an acidic pigment derivative and an electrically insulating liquid. CONSTITUTION:Since the acidic pigment derivative is colored, it is preferred to be used for the colorant same as the color, but it is not limited when the black colorant is used, and a suitable amount of it to be added is different according to the kind of pigment to be used, but in general, it is used in an amount of 0.1-30 weight % of the pigment, thus permitting the toner particles to be stabilized in dispersion and charged polarity, and a good image to be formed. Hydrocarbon solvents having a dielectric constant of <=3.5 and a volume resistivity of >=10<-7>OMEGA.cm are used for the insulating liquid, and polyacrylate and the like are used for the resin.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は静電潜像の顕在化に適用
される静電荷現像用液体現像剤に関し、さらに詳しく
は、顔料を樹脂中に酸性顔料誘導体の存在下で分散せし
めたトナー粒子と電気絶縁性液体とからなる静電荷現像
用液体現像剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a liquid developer for electrostatic charge development applied to the manifestation of an electrostatic latent image, and more specifically, a toner in which a pigment is dispersed in a resin in the presence of an acidic pigment derivative. The present invention relates to a liquid developer for electrostatic charge development, which comprises particles and an electrically insulating liquid.

【0002】[0002]

【従来の技術】静電荷現像用液体現像剤は、周知のごと
く、電気絶縁性の有機液体中にトナー粒子を分散させた
ものであり、そのトナー粒子は着色性、荷電性、定着
性、分散安定性 を必要とするために顔料、樹脂、その
他の添加剤が加わったものでトナー粒子を構成してい
る。このような静電荷現像用液体現像剤として以下のこ
とが重要となる。すなわち、(1)トナー粒子の分散安
定性が保たれていること(2)トナー粒子の帯電極性が
安定していること、である。
2. Description of the Related Art As is well known, a liquid developer for electrostatic charge development comprises toner particles dispersed in an electrically insulating organic liquid, and the toner particles are colored, charged, fixable and dispersed. Toner particles are made up of pigments, resins, and other additives that have been added in order to require stability. The following matters are important as such a liquid developer for electrostatic charge development. That is, (1) the dispersion stability of the toner particles is maintained, and (2) the charging polarity of the toner particles is stable.

【0003】以上の問題点を解決するために、例えば特
開昭50−17642号公報に述べられて いるよう
に、電気絶縁性液体に部分溶解する特殊な樹脂を添加す
ることにより、分散安定化を保証するような試みが提案
されている。また、特開昭51−37651号公報や特
開昭51−47437号公報に記載されているように特
殊な活性剤をトナーに添加することにより、分散安定を
保っている。さらに、特開昭50−70024では、あ
る特定の金属セッケンをトナーに加えることにより、帯
電の安定化の提案がなされている。
In order to solve the above problems, for example, as described in Japanese Patent Laid-Open No. 50-17642, dispersion stabilization is achieved by adding a special resin partially soluble in an electrically insulating liquid. Attempts have been made to ensure that. Moreover, dispersion stability is maintained by adding a special activator to the toner as described in JP-A-51-37651 and JP-A-51-47437. Further, Japanese Patent Application Laid-Open No. 50-70024 proposes stabilization of charging by adding a specific metal soap to the toner.

【0004】このような検討にもかかわらず、分散安定
化の目的で添加する活性剤の電気抵抗値が低いことに起
因して、電気絶縁性液体の抵抗が下がりすぎる、更に
は、帯電の安定化のために金属セッケンを添加した液体
現像剤の液抵抗の温度依存性が大きく、実用上新たな問
題が発生した。
In spite of the above studies, the resistance of the electrically insulating liquid is too low due to the low electric resistance of the activator added for the purpose of stabilizing the dispersion, and further the stability of the charging is stable. The temperature dependence of the liquid resistance of the liquid developer to which metal soap is added for the purpose of practical use is large, and a new problem has arisen in practical use.

【発明が解決しようとする課題】[Problems to be Solved by the Invention]

【0005】本発明は静電潜像の顕在化に適用される静
電荷現像用液体現像剤に関し、従来問題であったトナー
粒子の分散安定化と帯電極性の安定化を同時に改良し、
他の実用上の問題点をも解決した静電荷現像用液体現像
剤を提供するものである。
The present invention relates to a liquid developer for electrostatic charge development applied to the manifestation of an electrostatic latent image, and simultaneously improves the dispersion stabilization of toner particles and the stabilization of charging polarity, which have been problems in the past.
It is intended to provide a liquid developer for electrostatic charge development which solves other problems in practical use.

【課題を解決するための手段】[Means for Solving the Problems]

【0006】本発明は静電潜像の顕在化に適用される静
電荷現像用液体現像剤に関し、さらに詳しくは、顔料を
樹脂中に酸性顔料誘導体の存在下で分散せしめたトナー
粒子と電気絶縁性液体とからなる静電荷現像用液体現像
剤に関する。
The present invention relates to a liquid developer for electrostatic charge development applied to the manifestation of an electrostatic latent image, and more specifically, it is electrically insulated from toner particles in which a pigment is dispersed in a resin in the presence of an acidic pigment derivative. The present invention relates to a liquid developer for electrostatic charge development, which comprises a volatile liquid.

【0007】本発明に使用される酸性顔料誘導体は公知
のごとく、有色性であるため、好ましくは同色性の着色
剤に使用されるが、例えば黒色の着色剤を用いた場合
は、使用される顔料誘導体の種類は限定されない。
As is well known, the acidic pigment derivative used in the present invention is colored so that it is preferably used as a colorant having the same color. For example, when a black colorant is used, it is used. The type of pigment derivative is not limited.

【0008】本発明に用いられる顔料誘導体は下記一般
式(1)〜(3)で示される有機顔料を意味し、それら
の有機顔料が、アゾ系、フタロシアニン系、キナクリド
ン系、アントラキノン系、ペリレン系、ペリノン系、チ
オインジゴ系、ジオキサジン系、から選ばれるものであ
る。
The pigment derivative used in the present invention means organic pigments represented by the following general formulas (1) to (3), and those organic pigments are azo type, phthalocyanine type, quinacridone type, anthraquinone type and perylene type pigments. , Perinone-based, thioindigo-based, dioxazine-based.

【0009】一般式(1) Y−(SO3 Z/l)n (Y:有機顔料,Z/l;ZはCa,Ba,Sr,A
l、またはMn,lはZの価数を表す。もしくは、Z/
lで水素原子または のアミンを表す。R1 〜R4 ;水素原子または炭素数1
〜20のアルキル基を表す。ただし、R1 〜R4 が全て
水素原子である場合を除く。n;1〜4の整数。)
General formula (1) Y- (SO 3 Z / l) n (Y: organic pigment, Z / l; Z is Ca, Ba, Sr, A
1 or Mn, 1 represents the valence of Z. Or Z /
l is a hydrogen atom or Represents the amine. R 1 to R 4 ; hydrogen atom or carbon number 1
Represents an alkyl group of 20. However, the case where R 1 to R 4 are all hydrogen atoms is excluded. n; an integer of 1 to 4. )

【0010】一般式(2) Y−(COO・Z/l)n (Y:有機顔料、Z/l;ZはCa,Ba、Sr,A
l、またはMn,lはZの価数を表す。もしくは、Z/
lで水素原子または のアミンを表す。R1 〜R4 ;水素原子または炭素数1
〜20のアルキル基を表す。ただし、R1 〜R4 が全て
水素原子である場合を除く。n;1〜4の整数。)
General formula (2) Y- (COO.Z / l) n (Y: organic pigment, Z / l; Z is Ca, Ba, Sr, A
1 or Mn, 1 represents the valence of Z. Or Z /
l is a hydrogen atom or Represents the amine. R 1 to R 4 ; hydrogen atom or carbon number 1
Represents an alkyl group of 20. However, the case where R 1 to R 4 are all hydrogen atoms is excluded. n; an integer of 1 to 4. )

【0011】[0011]

【化1】 一般式(3) (Y:有機顔料、Z/l;ZはCa,Ba、Sr,A
l、またはMn,lはZの価数を表す。もしくは、Z/
lで水素原子または のアミンを表す。R1 〜R4 ;水素原子または炭素数1
〜20のアルキル基を表す。ただし、R1 〜R4 が全て
水素原子である場合を除く。n;1〜4の整数。X;水
素原子、ハロゲン原子、ニトロ基、アミノ基、スルホン
基、カルボキシル基またはアルキル基を表す。)
[Chemical 1] General formula (3) (Y: organic pigment, Z / l; Z is Ca, Ba, Sr, A
1 or Mn, 1 represents the valence of Z. Or Z /
l is a hydrogen atom or Represents the amine. R 1 to R 4 ; hydrogen atom or carbon number 1
Represents an alkyl group of 20. However, the case where R 1 to R 4 are all hydrogen atoms is excluded. n; an integer of 1 to 4. X: represents a hydrogen atom, a halogen atom, a nitro group, an amino group, a sulfone group, a carboxyl group or an alkyl group. )

【0012】一般式(1)〜(3)の例としては、化合
物(a)〜(d)を挙げることができる。
Examples of the general formulas (1) to (3) include compounds (a) to (d).

【0013】[0013]

【化2】 化合物(a)[Chemical 2] Compound (a)

【0014】[0014]

【化3】 化合物(b)[Chemical 3] Compound (b)

【0015】[0015]

【化4】 化合物(c)[Chemical 4] Compound (c)

【0016】[0016]

【化5】 化合物(d)[Chemical 5] Compound (d)

【0017】本発明の静電荷現像用液体現像剤において
酸性顔料誘導体は使用する顔料の種類によって適性添加
量が異なるが、一般的には顔料に対して0.1重量%か
ら30重量%の範囲で用いることにより、静電荷現像用
液体現像剤としての適性、すなわち(1)トナー粒子の
分散安定性が保たれていること(2)トナー粒子の帯電
極性が安定していること、さらに(3)良好な画像が形
成できた。
In the liquid developer for electrostatic charge development of the present invention, the suitable addition amount of the acidic pigment derivative varies depending on the kind of the pigment used, but it is generally in the range of 0.1% by weight to 30% by weight with respect to the pigment. The suitability as a liquid developer for electrostatic charge development, that is, (1) the dispersion stability of toner particles is maintained, (2) the charging polarity of toner particles is stable, and (3) ) A good image could be formed.

【0018】本発明で用いられる電気絶縁性液体は、誘
電率3.5以下、体積抵抗107 オームセンチ以上の炭
化水素系溶剤が用いられる。これらの好ましい例として
は、150〜220°Cの範囲に沸点を有する脂肪族炭
化水素、芳香族炭化水素およびこれらの混合物であり、
アイソパG,H,L(エッソ 製)、シェルゾールA,
AB(シェル 製)、ナフテゾルL,M,H(日本石油
製)等が挙げられる。
As the electrically insulating liquid used in the present invention, a hydrocarbon solvent having a dielectric constant of 3.5 or less and a volume resistance of 10 7 ohm cm or more is used. Preferred examples of these are aliphatic hydrocarbons, aromatic hydrocarbons and mixtures thereof having a boiling point in the range of 150 to 220 ° C,
Isopa G, H, L (made by Esso), Shersol A,
Examples include AB (made by Shell), Naphthesol L, M, H (made by Nippon Oil Co., Ltd.).

【0019】本発明で使用される樹脂としては、ポリア
クリル酸エステル、ポリメタクリル酸エステル等のアク
リル樹脂、ポリスチレン、ポリエチレン−アクリル酸共
重合体、ポリエチレン−メタクリル酸共重合体、ポリエ
チレン−酢酸ビニル共重合体等のポリエチレン系樹脂そ
の他ポリ塩化ビニル樹脂、ニトロセルロース、アルキッ
ド樹脂、フェノール樹脂、ポリエステル樹脂、ポリビニ
ルブチラール樹脂、ポリイソシアネート樹脂、ポリウレ
タン樹脂、ポリアミド樹脂,エポキシ樹脂などが挙げら
れるが、これらに限定されるものではない。
The resin used in the present invention includes acrylic resins such as polyacrylic acid ester and polymethacrylic acid ester, polystyrene, polyethylene-acrylic acid copolymer, polyethylene-methacrylic acid copolymer, polyethylene-vinyl acetate copolymer. Polyethylene resins such as polymers, polyvinyl chloride resins, nitrocellulose, alkyd resins, phenol resins, polyester resins, polyvinyl butyral resins, polyisocyanate resins, polyurethane resins, polyamide resins, epoxy resins, etc., but are not limited to these. It is not something that will be done.

【0020】本発明の静電荷現像用液体現像剤には電荷
調整剤を添加することができる。電荷付与剤としては、
ナフテン酸コバルト、ナフテン酸亜鉛、ナフテン酸銅、
ナフテン酸マンガン、レシチン、オクチル酸コバルト、
オクチル酸ジルコニウムなど一般に使用されるものを、
自由に使うことができる。
A charge control agent may be added to the liquid developer for electrostatic charge development of the present invention. As the charge-imparting agent,
Cobalt naphthenate, zinc naphthenate, copper naphthenate,
Manganese naphthenate, lecithin, cobalt octylate,
What is commonly used, such as zirconium octylate,
You can use it freely.

【0021】本発明の静電荷現像用液体現像剤の製造方
法は、顔料、樹脂、酸性顔料誘導体をサンドミルなどの
分散機により電気絶縁性液体中で湿式分散する方法、あ
らかじめ顔料、樹脂、酸性顔料誘導体を2本ロール、2
軸押出機などにより分散したのち、サンドミルにより湿
式分散する方法などがある。
The method for producing the liquid developer for electrostatic charge development of the present invention includes a method in which a pigment, a resin and an acidic pigment derivative are wet-dispersed in an electrically insulating liquid by a dispersing machine such as a sand mill. 2 rolls of the derivative, 2
There is a method in which the particles are dispersed by a shaft extruder or the like and then wet-dispersed by a sand mill.

【0022】[0022]

【実施例】以下実施例に基づいて本発明をさらに詳細に
説明する。なお、部とあるのは、重量部を、%とあるの
は、重量部%を示す。なお、画像評価は不揮発分1.5
%に希釈した現像液を液体現像複写機(Savin87
0:セイビン社製)にて得た画像物で行った。また、保
存安定性は50日後同様の方法で得られた画像物を用い
て評価を行った。
The present invention will be described in more detail based on the following examples. In addition, "parts" means "parts by weight" and "%" means "parts by weight". In addition, the image evaluation is a nonvolatile content of 1.5.
Liquid developer copier (Savin87
0: manufactured by Sabin Co., Ltd.). The storage stability was evaluated after 50 days using an image obtained by the same method.

【0023】実施例1 ポリエチレン樹脂 三井ハイワックス4202E(三井石油化学工業(株)製) 40部 カーボンブラック(三菱カラーカーボン#44 三菱化成工業(株)製) 2部 化合物(a) 0.01部 アイソパG(エクソン社) 160部Example 1 Polyethylene resin Mitsui High Wax 4202E (manufactured by Mitsui Petrochemical Industry Co., Ltd.) 40 parts Carbon black (Mitsubishi Color Carbon # 44 manufactured by Mitsubishi Kasei Co., Ltd.) 2 parts Compound (a) 0.01 part Isopa G (Exxon) 160 copies

【0024】上記混合物を30時間湿式分散し、濃縮現
像液を得た。アイソパGを加え固形分1.5%の現像液
に調整した。本現像液1000部にオクチル酸ジルコニ
ウムを0.2部添加して、画像評価用現像液とした。こ
れを画像評価マシンである、液体現像複写機に入れ得ら
れた画像のベタ部の濃度を反射濃度計(マクベス RZ
−918 マクベス社)により測定した結果1.38と
いう値を得た。また非画像部の汚れもなく良好な結果で
あった。さらに、所定の保存安定性の評価方法に従い、
50日後の画像出力を行い、初期との比較を行ったが、
特に変化は認められず、良好な結果を得た。結果を表1
に示す。
The above mixture was wet-dispersed for 30 hours to obtain a concentrated developer. Isopa G was added to adjust the developer to a solid content of 1.5%. 0.2 part of zirconium octylate was added to 1000 parts of the main developer to prepare a developer for image evaluation. This was put into a liquid development copying machine, which is an image evaluation machine, and the density of the solid portion of the obtained image was measured by a reflection densitometer (Macbeth
As a result of measurement by -918 Macbeth Co., Ltd., a value of 1.38 was obtained. In addition, there was no stain on the non-image area, which was a good result. Furthermore, according to a predetermined storage stability evaluation method,
The image was output after 50 days and compared with the initial one.
No particular change was observed and good results were obtained. The results are shown in Table 1.
Shown in.

【0025】比較例 実施例1の処方のうち銅フタロシアニン化合物を添加し
ないまま、同様の方法で濃縮現像液を得た。その後の試
料作成も同様に行い、画像評価用現像液を作り所定の方
法に従い画像を得た。その結果、ベタ部の濃度、非画像
部の汚れは、実施例1とほぼ同等であったが、保存安定
性の評価では、ベタ部の濃度、非画像部の汚れの点で実
用に適さないことが分かった。
Comparative Example A concentrated developer was prepared in the same manner as in Example 1 except that the copper phthalocyanine compound was not added. Subsequent sample preparation was performed in the same manner, a developer for image evaluation was prepared, and an image was obtained according to a predetermined method. As a result, the solid part density and the non-image part stain were almost the same as those in Example 1, but the evaluation of the storage stability was not suitable for practical use in terms of the solid part density and the non-image part stain. I found out.

【0026】実施例2 ポリエステル樹脂 エリテールUE−3210(ユニチカ(株)製) 40部 青色顔料 リオノールブルー FG7350(東洋インキ製造(株)製) 1.3部 化合物(b) 0.1部 アイソパL 160部Example 2 Polyester resin Elitere UE-3210 (manufactured by Unitika Ltd.) 40 parts Blue pigment Rionol Blue FG7350 (manufactured by Toyo Ink Mfg. Co., Ltd.) 1.3 parts Compound (b) 0.1 part Isopa L 160 copies

【0027】上記混合物を18時間湿式分散し、濃縮現
像液を得た。その後アイソパLを添加し、固形分1.5
%に調節した。本現像液1000部にナフテン酸コバル
ト0.2部加え、画像評価用現像液を作成した。画像評
価結果を表−1に示した。保存安定性の評価結果も表1
に示した。
The above mixture was wet-dispersed for 18 hours to obtain a concentrated developer. After that, Isopa L was added to give a solid content of 1.5.
Adjusted to%. 0.2 part of cobalt naphthenate was added to 1000 parts of the main developer to prepare a developer for image evaluation. The image evaluation results are shown in Table 1. The storage stability evaluation results are also shown in Table 1.
It was shown to.

【0028】実施例3 エポキシ樹脂 エピコート1004 (シェル社製) 40部 黄色顔料 リオノールイエローFG1308(東洋インキ(株)製) 1.5部 化合物(c) 3部Example 3 Epoxy resin Epicoat 1004 (manufactured by Shell Co.) 40 parts Yellow pigment Rionol Yellow FG1308 (manufactured by Toyo Ink Co., Ltd.) 1.5 parts Compound (c) 3 parts

【0029】以上の粉体を2軸の押出機で加熱混練し、
その後サンプルミルで粗砕したものを第2次原料とし
た。 第2次原料 20部 シェルゾールA 80部
The above powder is heated and kneaded by a twin-screw extruder,
Then, the material was roughly crushed with a sample mill and used as a secondary raw material. Secondary raw material 20 parts Shellzol A 80 parts

【0030】上記混合物を20時間湿式分散し、濃縮現
像液を得た。その後シェルゾールAにより、所定の濃度
に希釈し、現像液1000部にレシチン1部を添加し
て、画像評価用現像液とした。画像評価結果を表1に示
した。
The above mixture was wet-dispersed for 20 hours to obtain a concentrated developer. After that, it was diluted to a predetermined concentration with Shellzol A, and 1 part of lecithin was added to 1000 parts of the developing solution to obtain a developing solution for image evaluation. The image evaluation results are shown in Table 1.

【0031】実施例4 ポリエチレン−メタクリル酸共重合体 ハイミラン1856 (三井・ディポン ポリケミカル(株)製) 40部 紅色顔料 ブリリアントカーミン6BA (東洋インキ製造(株)製) 0.3部 化合物(d) 0.02部 ナフテゾルM 80部Example 4 Polyethylene-methacrylic acid copolymer Himilan 1856 (manufactured by Mitsui-Dipon Polychemical Co., Ltd.) 40 parts Red pigment Brilliant Carmine 6BA (manufactured by Toyo Ink Mfg. Co., Ltd.) 0.3 part Compound (d) 0.02 parts Naphthesol M 80 parts

【0032】上記混合物を35時間湿式分散し、濃縮現
像液を得た。その後ナフテゾルMにより所定の濃度に希
釈し、ナフテン酸マンガンを1.5%現像液1000部
に0.8部添加して、画像評価用現像液とした。画像評
価結果を表1に示した。
The above mixture was wet-dispersed for 35 hours to obtain a concentrated developer. After that, it was diluted to a predetermined concentration with Naphthesol M, and 0.8 part of manganese naphthenate was added to 1000 parts of 1.5% developer to prepare an image evaluation developer. The image evaluation results are shown in Table 1.

【0033】[0033]

【表1】 [Table 1]

【0034】[0034]

【発明の効果】本発明により静電潜像の顕在化に適用さ
れる静電荷現像用液体現像剤に関し、従来問題であった
トナー粒子の分散安定化と帯電極性の安定化を同時に改
良し、他の実用上の問題点をも解決した静電荷現像用液
体現像剤を提供できた。
The present invention relates to a liquid developer for electrostatic charge development which is applied to the manifestation of an electrostatic latent image according to the present invention, and simultaneously improves the dispersion stabilization of toner particles and the stabilization of charging polarity, which have been problems in the past. It has been possible to provide a liquid developer for electrostatic charge development that solves other practical problems.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】顔料を樹脂中に酸性顔料誘導体の存在下で
分散せしめたトナー粒子と電気絶縁性液体とからなる静
電荷現像用液体現像剤。
1. A liquid developer for electrostatic charge development comprising toner particles in which a pigment is dispersed in a resin in the presence of an acidic pigment derivative, and an electrically insulating liquid.
JP16434592A 1992-05-29 1992-05-29 Liquid developer for electrostatic charge development Expired - Lifetime JP3248243B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16434592A JP3248243B2 (en) 1992-05-29 1992-05-29 Liquid developer for electrostatic charge development

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16434592A JP3248243B2 (en) 1992-05-29 1992-05-29 Liquid developer for electrostatic charge development

Publications (2)

Publication Number Publication Date
JPH05333607A true JPH05333607A (en) 1993-12-17
JP3248243B2 JP3248243B2 (en) 2002-01-21

Family

ID=15791406

Family Applications (1)

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

Country Link
JP (1) JP3248243B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2590027A1 (en) 2011-11-04 2013-05-08 Konica Minolta Business Technologies, Inc. Liquid developer
JP2014074167A (en) * 2012-10-02 2014-04-24 Xerox Corp Phase change inks containing novel synergist
WO2014061747A1 (en) 2012-10-17 2014-04-24 東洋インキScホールディングス株式会社 Polymeric dispersant for liquid developers, liquid developer, and printed matter
WO2018131422A1 (en) 2017-01-13 2018-07-19 東洋インキScホールディングス株式会社 Liquid developer and method for producing printed material

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2590027A1 (en) 2011-11-04 2013-05-08 Konica Minolta Business Technologies, Inc. Liquid developer
US8974996B2 (en) 2011-11-04 2015-03-10 Konica Minolta Business Technologies, Inc. Liquid developer
JP2014074167A (en) * 2012-10-02 2014-04-24 Xerox Corp Phase change inks containing novel synergist
WO2014061747A1 (en) 2012-10-17 2014-04-24 東洋インキScホールディングス株式会社 Polymeric dispersant for liquid developers, liquid developer, and printed matter
US9523938B2 (en) 2012-10-17 2016-12-20 Toyo Ink Sc Holdings Co., Ltd. Polymeric dispersant for liquid developer, liquid developer, and printed matter
WO2018131422A1 (en) 2017-01-13 2018-07-19 東洋インキScホールディングス株式会社 Liquid developer and method for producing printed material

Also Published As

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