JPH08199093A - Water-based pigment composition - Google Patents

Water-based pigment composition

Info

Publication number
JPH08199093A
JPH08199093A JP3009995A JP3009995A JPH08199093A JP H08199093 A JPH08199093 A JP H08199093A JP 3009995 A JP3009995 A JP 3009995A JP 3009995 A JP3009995 A JP 3009995A JP H08199093 A JPH08199093 A JP H08199093A
Authority
JP
Japan
Prior art keywords
water
weight
pigment
compsn
parts
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
JP3009995A
Other languages
Japanese (ja)
Other versions
JP3702373B2 (en
Inventor
Akimitsu Kato
昭光 加藤
Yuichi Kobayashi
雄一 小林
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.)
Pentel Co Ltd
Original Assignee
Pentel 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 Pentel Co Ltd filed Critical Pentel Co Ltd
Priority to JP03009995A priority Critical patent/JP3702373B2/en
Publication of JPH08199093A publication Critical patent/JPH08199093A/en
Application granted granted Critical
Publication of JP3702373B2 publication Critical patent/JP3702373B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE: To obtain a water-based pigment compsn. reduced in viscosity increase even after the lapse of time by using a pigment, an acrylic ester emulsion, a high-boiling water-soluble solvent, a condensed naphthalenesulfonic acid salt, a substance represented by a specific formula, and water. CONSTITUTION: This compsn. comprises (A) a pigment, (B) an acrylic ester emulsion, (C) a high-boiling water-soluble solvent, (D) a condensed naphthalenesulfonic acid salt, (E) a substance of the formula (wherein R is 1-10C alkyl; n is a positive integer; and M is Na, K or NH4 ), and (F) water. A conventional water-based pigment compsn. for use as a poster color, a water color, etc., comprises the components (A), (B), (C), and (F). In this case, when the amt. of the component (A) to be blended is increased in order to improve the color development of the compsn. or increase the density thereof, the applicability of the compsn. is deteriorated due to the viscosity increase thereof with the lapse of time. The compsn., when further blended with the components (D) and (E), is reduced in viscosity increase with the lapse of time, and can therefore be esp. suitably used as water-resistant poster color and water color.

Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は、耐水性を有するポスタ
ーカラー、水彩絵具などに好適に用いられる水性顔料組
成物に関する。 【0002】 【従来の技術】耐水性を有するポスターカラー、水彩絵
具などとして用いられる水性顔料組成物は、顔料と、ア
クリル酸エステル系エマルジョンと、高沸点水溶性有機
溶剤と、水とよりなっていた。顔料は着色材として用い
られているものである。アクリル酸エステル系エマルジ
ョンは定着剤として用いられているものであり、塗布跡
に耐水性を付与するものである。高沸点水溶性有機溶剤
は凍結防止剤や乾燥時間調整剤として用いている。 【0003】 【発明が解決しようとする課題】ところで、上記のよう
な水性顔料組成物をポスターカラー、水彩絵具として使
用した場合、発色を良くするため、もしくは濃度を上げ
るために顔料の配合量を増やすと、経時的に水性顔料組
成物が増粘し絵の具の塗布性が悪くなるという問題が発
生する。 【0004】 【課題を解決するための手段】本発明は、経時後にも増
粘が少ない水性顔料組成物を得ることを目的としたもの
であって、顔料と、アクリル酸エステル系エマルジョン
と、高沸点水溶性溶剤と、縮合ナフタレンスルホン酸塩
と、化1で示す物質と、水とを少なくとも含むことを特
徴とする水性顔料組成物を要旨とする。 【0005】顔料は、着色材として使用する。従来公知
の各種無機顔料及び有機顔料を使用できる。具体的に
は、カーボンブラック、アニリンブラック、酸化チタ
ン、ベンガラ、カドミウムレッド、レーキレッド、カー
ミン3B、同6B、黄土、バリウム黄、ハンザエロー
G、同10G、群青、フタロシアニンブルー、フタロシ
アニングリーン等が挙げられる。これらの顔料は単独若
しくは複数混合して使用でき、その使用量は水性顔料組
成物全量に対して10〜50重量%が好ましい。 【0006】アクリル酸エステル系エマルジョンは、塗
布跡に耐水性を付与するものであって、展色剤としても
使用する。具体的には、メタクリル酸メチル、アクリル
酸メチル、アクリル酸エチル、メタクリル酸エチル、ア
クリル酸イソプロピル、メタクリル酸イソプロピル、ア
クリル酸ブチル、メタクリル酸ブチル等のエステルのエ
マルジョン、又は前記アクリル酸エステルやメタクリル
酸エステルを組み合わせた共重合体のエマルジョンなど
が挙げられる。その使用量は水性顔料組成物全量に対し
て5〜30重量%が好ましい。 【0007】高沸点水溶性有機溶剤は、凍結安定剤、乾
燥調整剤などとして使用するものであって、グリセリ
ン、エチレングリコール、プロピレングリコール、ジプ
ロピレングリコール、ソルビトール等が挙げられる。こ
の高沸点水溶性有機溶剤は、単独若しくは複数混合して
使用でき、その使用量は水性顔料組成物全量に対して1
〜10%重量が好ましい。 【0008】縮合ナフタレンスルホン酸塩は一般に顔料
分散剤として用いられ、縮合ナフタレンスルホン酸ナト
リウム塩、縮合ナフタレンスルホン酸カリウム塩、縮合
ナフタレンスルホン酸アンモニウム塩等が挙げられる。 【0009】化1で示す物質は一般にポリカルボン酸系
化合物といわれるものであって、顔料分散剤として用い
られることが知られている。 【0010】本発明においては、上記縮合ナフタレンス
ルホン酸塩と化1で示すポリカルボン酸系化合物とを併
用することによって、顔料とアクリル酸エステル系エマ
ルジョンとが含まれる組成物のゲル化を防止し、組成物
の安定性を向上することが可能となる。上記縮合ナフタ
レンスルホン酸塩と化1で示すポリカルボン酸系化合物
との使用量は、各々0.1〜10重量%が好ましい。 【0011】尚、上記成分の外、必要に応じて炭酸カル
シウム、硫酸バリウム等の体質顔料や、増粘材として、
カルボキシメチルセルロース、ヒドロキシエチルセルロ
ース、ヒドロキシフロピルセルロース等の水溶性高分子
を0.05〜2.0重量%用いたり、防腐・防黴剤、防
錆剤、脱泡・消泡剤などの添加剤を適宜用いても良い。 【0012】又、本発明の水性顔料組成物は、従来公知
の方法によって容易に得ることができる。例えば、上記
成分を三本ロールミルや横型ボールミル、横型ビーズミ
ル等の分散機にて混合分散するなどである。 【0013】 【作用】顔料の表面は、色々な物質を吸着する作用があ
り、発色を良くするため、又は濃度を高くするために顔
料の使用量を多くすると、定着剤として用いられている
アクリル酸エステル系エマルジョンの樹脂粒子表面の乳
化剤を顔料が吸着してしまい、アクリル酸エステル系エ
マルジョンを分解してしまう。そのため乳化剤を吸着し
た顔料の分散が悪くなり、増粘が起こる。縮合ナフタレ
ンスルホン酸塩と化1で示す物質は、各々が顔料表面に
相乗的に付着し、顔料がアクリル酸系エマルジョンの乳
化剤を吸着させない状態にすることが出来、増粘を防止
すると考えられる。 【0014】 【実施例】以下、実施例及び比較例を示すが、本発明
は、下記実施例に限定されるものではない。 【0015】実施例1 ハンザイエローG(C.I.ピグメントイエロー1) 10重量部 ポリアクリル酸エチルエマルジョン 10重量部 ヒドロキシメチルセルロース 0.5重量部 グリセリン 5重量部 縮合ナフタレンスルホン酸ナトリウム塩 0.5重量部 化1で示す物質(M:ナトリウム、R:エチル基) 0.5重量部 水 33重量部 ジエタノールアミン 0.5重量部 炭酸カルシウム 40重量部 上記成分をラボミキサーに入れ15分間撹拌した後、三
本ロールミルにて2回通しを行ない黄色の水性顔料組成
物を得た。 【0016】実施例2 カーミン6B(C.I.ピグメントレッド57) 5重量部 アクリル酸エチル−メタクリル酸ブチルの共重合体エマルジョン 15重量部 グリセリン 5重量部 縮合ナフタレンスルホン酸ナトリウム塩 3重量部 化1で示す物質(M:ナトリウム、R:プロピル基) 1重量部 水 40重量部 濃アンモニア水 0.5重量部 カルボキシルメチルセルロース 0.5重量部 炭酸カルシウム 30重量部 上記成分をラボミキサーに入れ15分間撹拌した後、三
本ロールミルにて2回通しを行ない赤色の水性顔料組成
物を得た。 【0017】実施例3 群青(C.I.ピグメントブルー29) 40重量部 アクリル酸ブチル−メタクリル酸メチル共重合体エマルジョン 12重量部 グリセリン 5重量部 縮合ナフタレンスルホン酸ナトリウム塩 1重量部 化1で示す物質(M:アンモニウム、R:ヘキシル基) 1重量部 水 37重量部 濃アンモニア水 0.5重量部 ヒドロキシプロピルセルロース 0.3重量部 酸化ケイ素 3重量部 上記成分をラボミキサーに入れ15分間撹拌した後、三
本ロールミルにて2回通しを行ない青色の水性顔料組成
物を得た。 【0018】実施例4 群青(C.I.ピグメントブルー29) 40重量部 アクリル酸ブチル−メタクリル酸エチルの共重合体エマルジョン 12重量部 グリセリン 5重量部 縮合ナフタレンスルホン酸アンモニウム塩 1重量部 化1で示す物質(M:カリウム、R:ヘキシル基) 1重量部 水 37重量部 濃アンモニア水 0.5重量部 ヒドロキシプロピルセルロース 0.3重量部 酸化ケイ素 3重量部 上記成分をラボミキサーに入れ15分間撹拌した後、三
本ロールミルにて2回通しを行ない青色の水性顔料組成
物を得た。 【0019】比較例1 実施例1において、縮合ナフタレンスルホン酸ナトリウ
ム塩0.5重量部と化1で示す物質0.5重量部とを、
顔料分散剤として知られているポリオキシエチレンドデ
シルエーテル1重量部に代えた以外は、実施例1と同様
になして黄色の水性顔料組成物を得た。 【0020】比較例2 実施例2において、縮合ナフタレンスルホン酸ナトリウ
ム塩3重量部と化1で示す物質1重量部とを、顔料分散
剤として知られているポリオキシエチレンドデシルフェ
ニルエーテル4重量部に代えた以外は、実施例2と同様
になして赤色の水性顔料組成物を得た。 【0021】比較例3 実施例3において、縮合ナフタレンスルホン酸ナトリウ
ム塩1重量部と化1で示す物質1重量部とを、水2重量
部に代えた以外は、実施例3と同様になして青色の水性
顔料組成物を得た。 【0022】上記、実施例1〜4、比較例1〜3で得た
水性顔料組成物について流動特性試験を行った。結果を
表1に示す。 【0023】流動特性試験 JIS K 5101 顔料試験法 10.1 スプレ
ッドメーター法にて3回測定した値の平均値を算出し
た。単位はmm。測定は、上記、実施例1〜4、比較例
1〜3で得た水性顔料組成物について、調製直後及び保
管後に行った。保管は、各々の水性顔料組成物60ml
を蓋付試験管に入れ、密封して室温で10日放置した。 【0024】 【表1】 【0025】 【発明の効果】以上詳細に説明したように、本発明に係
る水性顔料組成物は、経時的な増粘が少なく、耐水性の
ポスターカラー、水彩絵具として特に有用に用いられ
る。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a water-based pigment composition suitable for use in water resistant poster colors, watercolors and the like. A water-based pigment composition used as a water-resistant poster color, watercolor paint, etc. is composed of a pigment, an acrylic ester emulsion, a high-boiling point water-soluble organic solvent, and water. It was The pigment is used as a coloring material. The acrylic ester emulsion is used as a fixing agent, and imparts water resistance to the application mark. The high boiling water-soluble organic solvent is used as an antifreezing agent and a drying time adjusting agent. By the way, when the aqueous pigment composition as described above is used as a poster color or a watercolor paint, the amount of the pigment to be mixed is adjusted in order to improve the color development or increase the concentration. If the amount is increased, the aqueous pigment composition thickens with time and the coating property of the paint is deteriorated. SUMMARY OF THE INVENTION The present invention is intended to obtain an aqueous pigment composition having a small increase in viscosity even after a lapse of time. The gist is an aqueous pigment composition comprising at least a boiling point water-soluble solvent, a condensed naphthalene sulfonate, a substance represented by Chemical formula 1, and water. Pigments are used as colorants. Various conventionally known inorganic pigments and organic pigments can be used. Specifically, carbon black, aniline black, titanium oxide, red iron oxide, cadmium red, lake red, carmine 3B, 6B, ocher, barium yellow, Hansa Yellow G, 10G, ultramarine, phthalocyanine blue, phthalocyanine green and the like can be mentioned. . These pigments may be used alone or as a mixture of two or more, and the amount thereof is preferably 10 to 50% by weight based on the total amount of the aqueous pigment composition. [0006] The acrylic ester type emulsion imparts water resistance to a coating mark and is also used as a color developing agent. Specifically, emulsions of esters such as methyl methacrylate, methyl acrylate, ethyl acrylate, ethyl methacrylate, isopropyl acrylate, isopropyl methacrylate, butyl acrylate, and butyl methacrylate, or the above-mentioned acrylic ester or methacrylic acid. Examples thereof include emulsions of copolymers in which esters are combined. The amount used is preferably 5 to 30% by weight based on the total amount of the aqueous pigment composition. The high-boiling point water-soluble organic solvent is used as a freeze stabilizer, a drying regulator, etc., and examples thereof include glycerin, ethylene glycol, propylene glycol, dipropylene glycol and sorbitol. This high-boiling point water-soluble organic solvent can be used alone or as a mixture of two or more, and the amount used is 1 relative to the total amount of the aqueous pigment composition.
10% weight is preferred. The condensed naphthalene sulfonate is generally used as a pigment dispersant, and examples thereof include condensed naphthalene sulfonic acid sodium salt, condensed naphthalene sulfonic acid potassium salt, condensed naphthalene sulfonic acid ammonium salt and the like. The substance represented by Chemical formula 1 is generally called a polycarboxylic acid compound and is known to be used as a pigment dispersant. In the present invention, gelation of a composition containing a pigment and an acrylic ester emulsion is prevented by using the above-mentioned condensed naphthalene sulfonate and the polycarboxylic acid compound shown in Chemical formula 1 together. It becomes possible to improve the stability of the composition. The amount of each of the condensed naphthalene sulfonate and the polycarboxylic acid compound shown in Chemical formula 1 is preferably 0.1 to 10% by weight. In addition to the above components, if necessary, as an extender pigment such as calcium carbonate or barium sulfate, or a thickener,
0.05-2.0% by weight of water-soluble polymer such as carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose etc., or additives such as antiseptic / antifungal agent, antirust agent, defoaming / antifoaming agent, etc. You may use it suitably. The aqueous pigment composition of the present invention can be easily obtained by a conventionally known method. For example, the above components are mixed and dispersed by a disperser such as a three-roll mill, a horizontal ball mill, a horizontal bead mill. The surface of the pigment has the function of adsorbing various substances. When the amount of the pigment used is increased to improve the color development or to increase the concentration, the acrylic used as a fixing agent is used. The pigment adsorbs the emulsifier on the surface of the resin particles of the acid ester emulsion, and decomposes the acrylic ester emulsion. Therefore, the dispersion of the pigment that has adsorbed the emulsifier becomes poor and thickening occurs. It is considered that the condensed naphthalene sulfonate and the substance represented by Chemical Formula 1 are synergistically attached to the surface of the pigment, and the pigment can be in a state in which the emulsifier of the acrylic acid emulsion is not adsorbed, thus preventing thickening. EXAMPLES Examples and comparative examples will be shown below, but the present invention is not limited to the following examples. Example 1 Hansa Yellow G (CI Pigment Yellow 1) 10 parts by weight Polyacrylic acid ethyl emulsion 10 parts by weight Hydroxymethyl cellulose 0.5 parts by weight Glycerin 5 parts by weight Condensed naphthalene sulfonic acid sodium salt 0.5 parts by weight Part 1 Substance (M: sodium, R: ethyl group) 0.5 parts by weight Water 33 parts by weight Diethanolamine 0.5 parts by weight Calcium carbonate 40 parts by weight After the above ingredients are put in a lab mixer and stirred for 15 minutes, Two passes were performed on this roll mill to obtain a yellow aqueous pigment composition. Example 2 Carmine 6B (CI Pigment Red 57) 5 parts by weight Ethyl acrylate-butyl methacrylate copolymer emulsion 15 parts by weight Glycerin 5 parts by weight Condensed naphthalene sulfonic acid sodium salt 3 parts by weight Chemical formula 1 Substance (M: sodium, R: propyl group) 1 part by weight Water 40 parts by weight Concentrated ammonia water 0.5 parts by weight Carboxymethyl cellulose 0.5 parts by weight Calcium carbonate 30 parts by weight The above ingredients are placed in a lab mixer and stirred for 15 minutes. After that, the mixture was passed through a three-roll mill twice to obtain a red aqueous pigment composition. Example 3 Ultramarine (CI Pigment Blue 29) 40 parts by weight Butyl acrylate-methyl methacrylate copolymer emulsion 12 parts by weight Glycerin 5 parts by weight Condensed naphthalene sulfonic acid sodium salt 1 part by weight Substance (M: ammonium, R: hexyl group) 1 part by weight Water 37 parts by weight Concentrated ammonia water 0.5 parts by weight Hydroxypropyl cellulose 0.3 parts by weight Silicon oxide 3 parts by weight The above components were placed in a lab mixer and stirred for 15 minutes. Then, it was passed through a three-roll mill twice to obtain a blue water-based pigment composition. Example 4 Ultramarine (CI Pigment Blue 29) 40 parts by weight Butyl acrylate-ethyl methacrylate copolymer emulsion 12 parts by weight Glycerin 5 parts by weight Condensed naphthalene sulfonic acid ammonium salt 1 part by weight Substances shown (M: potassium, R: hexyl group) 1 part by weight Water 37 parts by weight Concentrated ammonia water 0.5 parts by weight Hydroxypropyl cellulose 0.3 parts by weight Silicon oxide 3 parts by weight The above components are put in a lab mixer and stirred for 15 minutes. After that, it was passed through a three-roll mill twice to obtain a blue aqueous pigment composition. Comparative Example 1 In Example 1, 0.5 part by weight of condensed sodium naphthalene sulfonate and 0.5 part by weight of the substance represented by Chemical Formula 1 were added.
A yellow aqueous pigment composition was obtained in the same manner as in Example 1 except that 1 part by weight of polyoxyethylene dodecyl ether known as a pigment dispersant was used. Comparative Example 2 In Example 2, 3 parts by weight of condensed sodium naphthalene sulfonate and 1 part by weight of the substance represented by Chemical Formula 1 were added to 4 parts by weight of polyoxyethylene dodecylphenyl ether known as a pigment dispersant. A red water-based pigment composition was obtained in the same manner as in Example 2 except that it was replaced. Comparative Example 3 Same as Example 3 except that 2 parts by weight of water was used instead of 1 part by weight of condensed sodium naphthalene sulfonate and 1 part by weight of the substance represented by Chemical formula 1. A blue aqueous pigment composition was obtained. The water-based pigment compositions obtained in Examples 1 to 4 and Comparative Examples 1 to 3 were subjected to a rheological property test. The results are shown in Table 1. Flow characteristic test JIS K 5101 Pigment test method 10.1 The average value of the values measured three times by the spread meter method was calculated. The unit is mm. The measurement was performed for the aqueous pigment compositions obtained in Examples 1 to 4 and Comparative Examples 1 to 3 immediately after preparation and after storage. Store 60 ml of each aqueous pigment composition
Was placed in a test tube with a lid, sealed and left at room temperature for 10 days. [Table 1] As described in detail above, the water-based pigment composition according to the present invention has little increase in viscosity over time, and is particularly useful as a water resistant poster color or watercolor paint.

Claims (1)

【特許請求の範囲】 顔料と、アクリル酸エステル系エマルジョンと、高沸点
水溶性溶剤と、縮合ナフタレンスルホン酸塩と、 【化1】 で示す物質と、水とを少なくとも含むことを特徴とする
水性顔料組成物。
Claims: A pigment, an acrylic ester emulsion, a high-boiling water-soluble solvent, a condensed naphthalene sulfonate, and An aqueous pigment composition comprising at least the substance shown in 1) and water.
JP03009995A 1995-01-26 1995-01-26 Aqueous pigment composition Expired - Lifetime JP3702373B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03009995A JP3702373B2 (en) 1995-01-26 1995-01-26 Aqueous pigment composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03009995A JP3702373B2 (en) 1995-01-26 1995-01-26 Aqueous pigment composition

Publications (2)

Publication Number Publication Date
JPH08199093A true JPH08199093A (en) 1996-08-06
JP3702373B2 JP3702373B2 (en) 2005-10-05

Family

ID=12294338

Family Applications (1)

Application Number Title Priority Date Filing Date
JP03009995A Expired - Lifetime JP3702373B2 (en) 1995-01-26 1995-01-26 Aqueous pigment composition

Country Status (1)

Country Link
JP (1) JP3702373B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003064311A (en) * 2001-08-23 2003-03-05 Shachihata Inc Coloring matter
JP2007009040A (en) * 2005-06-30 2007-01-18 Sumitomo Seika Chem Co Ltd Aqueous paint
CN101880488A (en) * 2010-07-16 2010-11-10 郑希林 Gold glistening pigment and preparation method thereof
JP2012207103A (en) * 2011-03-29 2012-10-25 Nippon Shokubai Co Ltd Resin composition for coating

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003064311A (en) * 2001-08-23 2003-03-05 Shachihata Inc Coloring matter
JP2007009040A (en) * 2005-06-30 2007-01-18 Sumitomo Seika Chem Co Ltd Aqueous paint
CN101880488A (en) * 2010-07-16 2010-11-10 郑希林 Gold glistening pigment and preparation method thereof
JP2012207103A (en) * 2011-03-29 2012-10-25 Nippon Shokubai Co Ltd Resin composition for coating

Also Published As

Publication number Publication date
JP3702373B2 (en) 2005-10-05

Similar Documents

Publication Publication Date Title
RU2740756C2 (en) Dispersive paint
JP5279266B2 (en) Use of water-soluble acrylic copolymers in optionally colored aqueous formulations and the resulting formulations
JP3702373B2 (en) Aqueous pigment composition
JP5827582B2 (en) Aqueous drawing material composition
JPH07145289A (en) Water-based pigment composition
WO2003064542A1 (en) Amphilic active pigment compounding agent
JP3663807B2 (en) Black pigment composition
JP5142451B2 (en) Aqueous pigment composition
JP3682694B2 (en) Aqueous pigment composition
JP2018158991A (en) Aqueous paint composition
JP6543427B1 (en) Aqueous paint composition
JP4538982B2 (en) Aqueous pigment composition
JPH07102191A (en) Aqueous pigment composition
JP2808655B2 (en) Print ink composition
JP3941625B2 (en) Aqueous pigment composition
JP3964743B2 (en) Water-based ink composition
JP3865873B2 (en) Erasable colorant composition
JPH1067963A (en) Water base fluorescent pigment composition
JP3116640B2 (en) Blue pigment composition
JPS6377977A (en) Pigment composition
JP3104454B2 (en) Blue pigment composition
JPH04139272A (en) Water-base pigment ink composition
JPS59120667A (en) Water-base pigment ink
JP2024046519A (en) water-based paint composition
JP3938329B2 (en) Aqueous pigment dispersion, method for producing the same, and aqueous ink composition

Legal Events

Date Code Title Description
A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20050323

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20050704

R150 Certificate of patent (=grant) or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080729

Year of fee payment: 3

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090729

Year of fee payment: 4

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090729

Year of fee payment: 4

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100729

Year of fee payment: 5

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100729

Year of fee payment: 5

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110729

Year of fee payment: 6

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120729

Year of fee payment: 7

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120729

Year of fee payment: 7

FPAY Renewal fee payment (prs date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130729

Year of fee payment: 8

EXPY Cancellation because of completion of term