JPH10110129A - Recording solution for ink-jet - Google Patents

Recording solution for ink-jet

Info

Publication number
JPH10110129A
JPH10110129A JP26571996A JP26571996A JPH10110129A JP H10110129 A JPH10110129 A JP H10110129A JP 26571996 A JP26571996 A JP 26571996A JP 26571996 A JP26571996 A JP 26571996A JP H10110129 A JPH10110129 A JP H10110129A
Authority
JP
Japan
Prior art keywords
pigment
recording liquid
solvent
ink jet
jet recording
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
JP26571996A
Other languages
Japanese (ja)
Other versions
JP3141792B2 (en
Inventor
Jun Satake
順 佐武
Hisatsugu Uraki
久嗣 浦木
Toshifumi Kamimura
敏文 上村
Yasuharu Iida
保春 飯田
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 JP26571996A priority Critical patent/JP3141792B2/en
Priority to US08/944,437 priority patent/US5928419A/en
Priority to DE69709015T priority patent/DE69709015T2/en
Priority to DE69710878T priority patent/DE69710878T2/en
Priority to EP98119588A priority patent/EP0894835B1/en
Priority to EP97307934A priority patent/EP0834537B1/en
Publication of JPH10110129A publication Critical patent/JPH10110129A/en
Application granted granted Critical
Publication of JP3141792B2 publication Critical patent/JP3141792B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain the subject recording solution capable of developing excellent dispersion stability and delivery stability at a nozzle, by dispersing a specific treated pigment into an aqueous liquid. SOLUTION: This recording solution is obtained by dispersing (B) a treated pigment (e.g. one having 10-150nm average particle diameter obtained by laser light scattering method) which is prepared by dispersing an organic pigment (B1 ) such as a quinacridone-based pigment or a phthalocyanine-based pigment into a solvent (B2 ) having no reactivity to sulfonic acid such as N-methyl-2- pyrrolidone or sulfolane and treating the organic pigment with a sulfonating agent (B3 ) such as a sulfonated pyridine salt or sulfamic acid into (A) an aqueous liquid. Preferably, the recording solution comprises O.1-10wt.% of the solid content of the component B with respect to dispersibility. The component B is considered to contain a sulfonic group on the surface of its particle so that improvement in dispersibility of the component B to the component A and reduction in size of the dispersion can be actualized.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は,分散安定性に優
れ,ノズルでの吐出安定性の良好なインクジェット用記
録液に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an ink jet recording liquid having excellent dispersion stability and good nozzle ejection stability.

【0002】[0002]

【従来の技術】従来よりインクジェット用記録液として
は,特開昭53−61412号公報,特開昭54−89
811号公報,特開昭55−65269号公報に開示さ
れているように,酸性染料,直接染料,塩基性染料等の
水溶性染料をグリコール系溶剤と水に溶解したものがよ
く用いられている。しかし,水溶性染料としては,記録
液の安定性を得るため,水に対する溶解性の高いものが
一般的に用いられており,インクジェット記録物の耐水
性が悪く,水をこぼしたりすると容易に記録部分の染料
のにじみを生じるという問題があった。
2. Description of the Related Art Conventionally, ink jet recording liquids have been disclosed in JP-A-53-61412 and JP-A-54-89.
As disclosed in JP-A-811 and JP-A-55-65269, those obtained by dissolving a water-soluble dye such as an acid dye, a direct dye or a basic dye in a glycol solvent and water are often used. . However, as the water-soluble dye, a dye having high solubility in water is generally used in order to obtain the stability of the recording liquid, and the ink-jet recorded matter has poor water resistance and is easily recorded when water is spilled. There was a problem that bleeding of some dyes occurred.

【0003】このような耐水性の不良を改良するため,
特開昭56−57862号公報に開示されているよう
に,染料の構造を変えたり,塩基性の強い記録液を調製
することが試みられている。また,特開昭50−490
04号公報,特開昭57−36692号公報,特開昭5
9−20696号公報,特開昭59−146889号公
報に開示されているように,記録紙と記録液との反応を
うまく利用して耐水性の向上を図ることも行われてい
る。これらの方法は,特定の記録紙については著しい効
果をあげているが,記録紙の制約を受けるという点で汎
用性に欠け、特定の記録紙以外を用いた場合は、水溶性
染料を使用する記録液では記録物の充分な耐水性が得ら
れないことが多い。
In order to improve such poor water resistance,
As disclosed in JP-A-56-57862, attempts have been made to change the structure of a dye or to prepare a recording solution having a strong basicity. Also, Japanese Patent Laid-Open No. 50-490
No. 04, JP-A-57-36692, JP-A-57-36692.
As disclosed in Japanese Patent Application Laid-Open No. 9-20696 and Japanese Patent Application Laid-Open No. Sho 59-146889, improvement of water resistance has also been attempted by making good use of the reaction between recording paper and a recording liquid. Although these methods have a remarkable effect on specific recording paper, they lack versatility in that they are restricted by recording paper, and use water-soluble dyes when other than specific recording paper is used. In many cases, the recording liquid cannot provide sufficient water resistance of the recorded matter.

【0004】また,耐水性の良好な記録液としては,油
溶性染料を高沸点溶剤に分散ないし溶解したもの,油溶
性染料を揮発性の溶剤に溶解したものがあるが,溶剤の
臭気や溶剤の排出の問題があり、環境上好ましくない。
また,大量の記録を行う場合や装置の設置場所によって
は,溶剤回収等が必要になるという問題がある。そこ
で、記録物の耐水性をよくするために,水系媒体に顔料
を分散した記録液の開発が行われている。
As recording liquids having good water resistance, there are those in which an oil-soluble dye is dispersed or dissolved in a high boiling point solvent, and those in which an oil-soluble dye is dissolved in a volatile solvent. There is a problem of emission of water, which is environmentally unfavorable.
In addition, there is a problem that solvent recovery or the like is required depending on a case where a large amount of recording is performed or where the apparatus is installed. Therefore, in order to improve the water resistance of the recorded matter, a recording liquid in which a pigment is dispersed in an aqueous medium has been developed.

【0005】しかし,顔料は,染料と異なり微小粒子と
して分散させることおよび分散状態を安定に保つことが
非常に困難である。一方,インクジェット用の記録液に
おいては,プリンターの高解像度化につれノズル径が細
くなってきており,これに伴い顔料の粒子径も微細化す
る必要が生じている。また,オーバーヘッドプロジェク
ター等の透明基材への画像形成においても染料並みの透
明性に対する要求があり,顔料の発色の観点からも微細
化が要求されている。
However, it is very difficult to disperse pigments as fine particles unlike dyes and to keep the dispersion state stable. On the other hand, in the recording liquid for ink jet, the nozzle diameter is becoming narrower as the resolution of the printer is increased, and accordingly, the particle diameter of the pigment needs to be made finer. Further, there is a demand for transparency on a par with dyes in forming an image on a transparent base material such as an overhead projector, and miniaturization is also demanded from the viewpoint of pigment coloring.

【0006】[0006]

【発明が解決しようとする課題】本発明の目的は,上記
従来の問題点を解決し,安定な分散性を有し,ノズルで
の吐出安定性の良好な水性インクジェット用記録液を提
供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to solve the above-mentioned conventional problems and to provide an aqueous ink jet recording liquid having stable dispersibility and good ejection stability at a nozzle. It is in.

【0007】[0007]

【課題を解決するための手段】本発明者らは,水性の液
体中に有機顔料を分散してなるインクジェット用記録液
において,スルホン酸との反応性を有さない溶剤中に分
散したのちスルホン化剤により処理した処理顔料を用い
ることにより,安定な分散性を有し,ノズルでの吐出安
定性の良好な水性インクジェット用記録液が得られるこ
とを見出し,本発明に至った。スルホン化剤により有機
顔料の表面を処理してなる処理顔料は,顔料の粒子表面
にスルホン酸基を有していると考えられ,処理された顔
料表面の働きにより水への分散性の向上と微小化が可能
となる。
Means for Solving the Problems The inventors of the present invention have proposed an ink jet recording liquid in which an organic pigment is dispersed in an aqueous liquid, after dispersing it in a solvent having no reactivity with sulfonic acid, It has been found that by using a treated pigment treated with an agent, an aqueous inkjet recording liquid having stable dispersibility and excellent ejection stability at a nozzle can be obtained, and the present invention has been accomplished. The treated pigment obtained by treating the surface of an organic pigment with a sulfonating agent is considered to have sulfonic acid groups on the surface of the pigment particles, and the dispersibility in water is improved by the function of the treated pigment surface. Miniaturization becomes possible.

【0008】すなわち,本発明は,水性の液体中に有機
顔料を分散してなるインクジェット用記録液において,
該有機顔料が,スルホン酸との反応性を有さない溶剤中
に有機顔料を分散し,しかるのちスルホン化剤により処
理した処理顔料であることを特徴とするインクジェット
用記録液に関する。また,本発明は,水性の液体中に有
機顔料を分散してなるインクジェット用記録液におい
て,該有機顔料が,顔料の粒子内部に実質的にスルホン
酸基を有さず,顔料の粒子表面にスルホン酸基を有する
処理顔料であることを特徴とするインクジェット用記録
液に関する。
That is, the present invention provides an ink jet recording liquid comprising an organic pigment dispersed in an aqueous liquid,
The present invention relates to a recording liquid for inkjet, wherein the organic pigment is a treated pigment obtained by dispersing the organic pigment in a solvent having no reactivity with sulfonic acid and then treating the organic pigment with a sulfonating agent. Further, the present invention provides an ink jet recording liquid comprising an organic pigment dispersed in an aqueous liquid, wherein the organic pigment has substantially no sulfonic acid group inside the pigment particle, and The present invention relates to an inkjet recording liquid, which is a treated pigment having a sulfonic acid group.

【0009】本発明に用いられる有機顔料としては,ト
ルイジンレッド,トルイジンマルーン,ハンザエロー,
ベンジジンエロー,ピラゾロンレッドなどの不溶性アゾ
顔料,リトールレッド,ヘリオボルドー,ピグメントス
カーレット,パーマネントレッド2Bなどの溶性アゾ顔
料,アリザリン,インダントロン,チオインジゴマルー
ンなどの建染染料からの誘導体,フタロシアニンブル
ー,フタロシアニングリーンなどのフタロシアニン系顔
料,キナクリドンレッド,キナクリドンマゼンタなどの
キナクリドン系顔料,ペリレンレッド,ペリレンスカー
レットなどのペリレン系顔料,イソインドリノンエロ
ー,イソインドリノンオレンジ,などのイソインドリノ
ン系顔料,ピランスロンレッド,ピランスロンオレンジ
などのピランスロン系,チオインジゴ系顔料,縮合アゾ
系顔料,ベンズイミダゾロン系顔料,フラバンスロンエ
ロー,アシルアミドエロー,キノフタロンエロー,ニッ
ケルアゾエロー,銅アゾメチンエロー,ペリノンオレン
ジ,アンスロンオレンジ,ジアンスラキノニルレッド,
ジオキサジンバイオレット等が例示できる。
The organic pigments used in the present invention include toluidine red, toluidine maroon, Hansa Yellow,
Insoluble azo pigments such as benzidine yellow and pyrazolone red; soluble azo pigments such as litol red, helio bordeaux, pigment scarlet and permanent red 2B; derivatives from vat dyes such as alizarin, indanthrone, and thioindigo maroon; phthalocyanine blue; Phthalocyanine pigments such as phthalocyanine green; quinacridone pigments such as quinacridone red and quinacridone magenta; perylene pigments such as perylene red and perylene scarlet; isoindolinone pigments such as isoindolinone yellow and isoindolinone orange; Pyranthrone-based pigments such as red and pyranthrone orange, thioindigo-based pigments, condensed azo-based pigments, benzimidazolone-based pigments, flavanthrone yellow, acylamidoe Over, quinophthalone yellow, nickel azo yellow, copper Azomechin'ero, perinone orange, Anse Ron orange, Dianthraquinonyl Red,
Dioxazine violet and the like can be exemplified.

【0010】なかでも,キナクリドン系顔料、フタロシ
アニン系顔料、ベンズイミダゾロン系顔料,イソインド
リノン系顔料およびキノフタロン系顔料からなる群より
選ばれる少なくとも1種の有機顔料を用いることが耐光
性等の点から好ましい。有機顔料は,微細な粒子のもの
が好ましく,平均粒径10〜150nm(レーザ散乱法
による測定値)のものが良好である。
[0010] Among them, the use of at least one organic pigment selected from the group consisting of quinacridone pigments, phthalocyanine pigments, benzimidazolone pigments, isoindolinone pigments and quinophthalone pigments is advantageous in terms of light resistance and the like. Is preferred. The organic pigment preferably has fine particles, and preferably has an average particle diameter of 10 to 150 nm (measured by a laser scattering method).

【0011】本発明に用いられるスルホン酸との反応性
を有さない溶剤は,有機顔料が不溶解または難溶解な溶
剤であり,活性プロトンを有さないもの,特にN−メチ
ル−2−ピロリドンまたはスルホランが好適である。ス
ルホン酸との反応性を有さない溶剤は,有機顔料の溶剤
による濡れおよび有機顔料のほぐれ状態を維持し,有機
顔料をスルホン化剤で良好に処理するためには,有機顔
料の3〜200重量倍用いることが好ましい。溶剤の量
が有機顔料の3重量よりも少ないと,有機顔料が凝集状
態のまま処理される可能性が高く,微小な粒子が得られ
にくい。一方,200重量倍よりも多いと,スルホン化
剤の反応性に悪影響がでたり,後の溶剤の除去,洗浄処
理が多大で顔料の回収工程が大変になる。また,有機顔
料の実質的な処理量が少なくなる。
The solvent having no reactivity with sulfonic acid used in the present invention is a solvent in which the organic pigment is insoluble or hardly soluble, and has no active proton, especially N-methyl-2-pyrrolidone. Or sulfolane is preferred. Solvents having no reactivity with sulfonic acid maintain the wetting of the organic pigment by the solvent and the state in which the organic pigment is unraveled. It is preferable to use it by weight. If the amount of the solvent is less than 3% by weight of the organic pigment, there is a high possibility that the organic pigment is treated in an aggregated state, and it is difficult to obtain fine particles. On the other hand, if the amount is more than 200 times by weight, the reactivity of the sulfonating agent is adversely affected, and the subsequent solvent removal and washing treatments are large, making the pigment recovery process difficult. In addition, the substantial processing amount of the organic pigment is reduced.

【0012】本発明に用いられるスルホン化剤として
は,スルホン化ピリジン塩,スルファミン酸,アミド硫
酸,フルオロ硫酸,クロロ硫酸,三酸化硫黄,発煙硫
酸,硫酸等が挙げられ,なかでも,スルホン化ピリジン
塩またはスルファミン酸が好適である。スルホン化剤
は,単独または2種以上を混合して用いることができ
る。スルホン化剤による処理は,有機顔料をスルホン酸
との反応性を有さない溶剤に分散し,スルホン化剤を添
加したのち60〜200℃に加熱し,あるいは60〜2
00℃に加熱したのちスルホン化剤を添加し,0.5〜
5時間攪拌することにより行う。攪拌は,予めハイスピ
ードミキサー等で高速攪拌し,スラリー状としたのち,
穏やかな攪拌に移行してもよく,高速の攪拌を継続しな
がら加熱処理を行ってもよい。また,加熱処理後にはじ
めて,高速の攪拌を行ってもよい。
Examples of the sulfonating agent used in the present invention include sulfonated pyridine salts, sulfamic acid, amidosulfuric acid, fluorosulfuric acid, chlorosulfuric acid, sulfur trioxide, fuming sulfuric acid, sulfuric acid and the like. Salts or sulfamic acids are preferred. The sulfonating agents can be used alone or in combination of two or more. In the treatment with the sulfonating agent, the organic pigment is dispersed in a solvent having no reactivity with sulfonic acid, and after adding the sulfonating agent, the mixture is heated to 60 to 200 ° C.
After heating to 00 ° C, the sulfonating agent is added,
Perform by stirring for 5 hours. Stirring is performed in advance by high-speed stirring using a high-speed mixer, etc., to form a slurry.
The process may shift to gentle stirring, or the heat treatment may be performed while continuing high-speed stirring. High-speed stirring may be performed only after the heat treatment.

【0013】加熱処理した後,顔料のスラリーから,ス
ルホン酸との反応性を有さない溶剤および残留するスル
ホン化剤を取り除く。取り除きは,水洗,限外濾過,逆
浸透等の方法,遠心分離,濾過等を繰り返して行う。処
理顔料のレーザ散乱法により測定した平均粒径は,10
〜150nm,さらには10〜100nmであることが
好ましい。このような粒径の処理顔料を用いると,記録
液の製造における濾過操作が容易であり,記録液を保存
した場合に経時での顔料の沈降も少ない。処理顔料は,
インクジェット用記録液100重量部中に固形分で0.
1〜10重量部の範囲で含まれることが分散性の点で好
ましい。
After the heat treatment, the solvent having no reactivity with sulfonic acid and the remaining sulfonating agent are removed from the pigment slurry. Removal is carried out by repeating washing, ultrafiltration, reverse osmosis, etc., centrifugation, filtration and the like. The average particle size of the treated pigment measured by the laser scattering method is 10
It is preferably from 150 to 150 nm, more preferably from 10 to 100 nm. When a treated pigment having such a particle size is used, the filtering operation in the production of the recording liquid is easy, and the sedimentation of the pigment over time is small when the recording liquid is stored. The treated pigment is
The solid content in 100 parts by weight of the recording liquid for ink jet is 0.1%.
It is preferable from the viewpoint of dispersibility that the amount is contained in the range of 1 to 10 parts by weight.

【0014】スルホン化処理を行った処理顔料は,10
〜40重量%程度の濃度になるように水性の液体中に添
加してそのまま,あるいは通常の分散を短時間行うこと
により,顔料の乾燥工程を経ずに,容易に水性顔料分散
体とすることができる。この水性顔料分散体は,分散剤
の添加をしなくとも良好な分散性を示す処理顔料微粒子
の分散体であるため,単に印字に適する濃度に希釈し,
必要に応じてさらに添加剤を加え,濾過することによ
り,インクジェット用記録液とすることができるが,さ
らに分散剤等を用い分散機による分散を行い,安定で定
着性の強いインクジェット用記録液とすることが好まし
い。サンドミル等の通常の分散機でさらに分散を行う
と,顔料が微細であり,安定した分散状態のインクジェ
ット用記録液が,分散時間を多大にかけることなく短時
間でかつ容易に得られる。
The treated pigment subjected to the sulfonation treatment is 10
An aqueous pigment dispersion can be easily obtained by adding it to an aqueous liquid so as to have a concentration of about 40% by weight or by performing normal dispersion for a short time without passing through a pigment drying step. Can be. Since this aqueous pigment dispersion is a dispersion of treated pigment fine particles showing good dispersibility without adding a dispersant, it is simply diluted to a concentration suitable for printing.
If necessary, an additive can be added and filtered to obtain an ink jet recording liquid. However, the ink is dispersed with a dispersing machine using a dispersant or the like to obtain a stable and highly fixable ink jet recording liquid. Is preferred. When the dispersion is further carried out using a usual dispersing machine such as a sand mill, the ink jet recording liquid in which the pigment is fine and in a stable dispersion state can be easily obtained in a short time without significantly increasing the dispersion time.

【0015】インクジェット用記録液の製造には,サン
ドミル,ホモジナイザー,ボールミル,ペイントシェー
カー,超音波分散機.高圧の室内にてキャビテーション
効果で分散する分散機等を用いることができる。また,
混合攪拌は,通常の羽を用いた攪拌機による攪拌のほ
か,高速の分散機,乳化機等により行うことができる。
For the production of an ink jet recording liquid, a sand mill, a homogenizer, a ball mill, a paint shaker, an ultrasonic disperser. A disperser or the like that disperses by a cavitation effect in a high-pressure room can be used. Also,
Mixing and stirring can be performed by a high-speed disperser, emulsifier, or the like, in addition to stirring by a stirrer using a normal blade.

【0016】本発明のインクジェット用記録液は、孔径
3μm以下のフィルター,好ましくは1.0μm以下の
フィルター,さらに好ましくは0.45μm以下のフィ
ルターにて十分濾過することが好ましい。フィルターの
濾過に先立って,遠心分離によって大きな粒径のものを
除くこともでき,これによってフィルターによる濾過に
おける目詰まりを少なくし,フィルターの使用期間が長
くなる。
The ink jet recording liquid of the present invention is preferably sufficiently filtered through a filter having a pore size of 3 μm or less, preferably a filter having a pore size of 1.0 μm or less, and more preferably a filter having a pore size of 0.45 μm or less. Prior to filtration of the filter, it is also possible to remove those having a large particle size by centrifugation, thereby reducing clogging in the filtration by the filter and prolonging the service life of the filter.

【0017】水性の液体としては,水および必要に応じ
て水性溶剤を用いることができる。水としては,金属イ
オン等を除去したイオン交換水ないし蒸留水を用いるこ
とができ,水は記録液中に50〜98重量%の範囲で含
まれることが好ましい。水性溶剤は,記録液のノズル部
分での乾燥,固化を防止し,記録液を安定して噴射さ
せ,保湿剤としても働くものであり,単独または混合し
て記録液中に0〜25重量%の範囲で用いることが好ま
しい。
As the aqueous liquid, water and, if necessary, an aqueous solvent can be used. As the water, ion-exchanged water or distilled water from which metal ions and the like have been removed can be used, and the water is preferably contained in the recording liquid in a range of 50 to 98% by weight. The aqueous solvent prevents drying and solidification of the recording liquid at the nozzle portion, stably sprays the recording liquid, and also functions as a humectant. It is preferable to use within the range.

【0018】水性溶剤としては,エチレングリコール,
ジエチレングリコール,プロピレングリコール,トリエ
チレングリコール,ポリエチレングリコール,グリセリ
ン,テトラエチレングリコール,ジプロピレングリコー
ル,ケトンアルコール,ジエチレングリコールモノブチ
ルエーテル,エチレングリコールモノブチルエーテル,
エチレングリコールモノエチルエーテル,1,2−ヘキ
サンジオール,N−メチル−2−ピロリドン,置換ピロ
リドン,2,4,6−ヘキサントリオール,テトラフル
フリルアルコール,4−メトキシ−4メチルペンタノン
等を例示できる。また,記録液の乾燥を速める目的にお
いては,メタノール,エタノール,イソプロピルアルコ
ール等のアルコール類も用いることができる。
As the aqueous solvent, ethylene glycol,
Diethylene glycol, propylene glycol, triethylene glycol, polyethylene glycol, glycerin, tetraethylene glycol, dipropylene glycol, ketone alcohol, diethylene glycol monobutyl ether, ethylene glycol monobutyl ether,
Examples include ethylene glycol monoethyl ether, 1,2-hexanediol, N-methyl-2-pyrrolidone, substituted pyrrolidone, 2,4,6-hexanetriol, tetrafurfuryl alcohol, and 4-methoxy-4-methylpentanone. . Further, alcohols such as methanol, ethanol and isopropyl alcohol can be used for the purpose of speeding up drying of the recording liquid.

【0019】本発明のインクジェット用記録液は,被印
刷体への定着性を強固にするため,水性樹脂を含むこと
が好ましい。水性樹脂は,処理顔料の分散性にも寄与す
る。なお,被印刷体がインキ受理性を有する場合には,
水性樹脂は必要ない。水性樹脂としては,水に溶解する
水溶解性の樹脂や,水に分散する水分散性のエマルショ
ン樹脂,コロイダルディスパーション樹脂が,それぞれ
単独ないし混合して用いられる。水性樹脂として具体的
には,アクリル系,スチレン−アクリル系,ポリエステ
ル系,ポリアミド系,ポリウレタン系,フッソ系等の水
溶解性樹脂および水分散性樹脂が挙げられる。
The ink jet recording liquid of the present invention preferably contains an aqueous resin in order to strengthen the fixability to a printing medium. The aqueous resin also contributes to the dispersibility of the treated pigment. If the printing medium has ink acceptability,
No aqueous resin is required. As the aqueous resin, a water-soluble resin that dissolves in water, a water-dispersible emulsion resin that disperses in water, and a colloidal dispersion resin are used alone or in combination. Specific examples of the water-based resin include water-soluble resins and water-dispersible resins such as acrylic, styrene-acryl, polyester, polyamide, polyurethane, and fluorine.

【0020】被印刷体への定着性を目的とするときに
は,水性樹脂は,記録液中に0.1〜10重量%の範囲
で用いられることが好ましい。この量よりも少ないと,
顔料を強固に定着できない。また,この量よりも多くな
ると,記録液の粘度が上昇しすぎたり吐出安定性が低下
したりするようになる。なお,水性樹脂として水溶解性
の樹脂を用いた場合、記録液の粘度を高くする傾向があ
るが,水分散性の樹脂では粘度を低く抑えることができ
たり、また,記録物の耐水性をより向上させることがで
きる。水性樹脂を用いる場合には,アンモニア,アミ
ン,無機アルカリ等の中和剤を加え,水性樹脂の溶解な
いし分散の安定性を調整することが好ましい。
For the purpose of fixing to a printing medium, the aqueous resin is preferably used in the recording liquid in the range of 0.1 to 10% by weight. If less than this amount,
The pigment cannot be fixed firmly. On the other hand, if the amount is larger than this amount, the viscosity of the recording liquid will increase too much or the ejection stability will decrease. When a water-soluble resin is used as the water-based resin, the viscosity of the recording liquid tends to be high, but the viscosity of the water-dispersible resin can be reduced or the water resistance of the recorded matter can be reduced. It can be further improved. When an aqueous resin is used, it is preferable to add a neutralizing agent such as ammonia, an amine or an inorganic alkali to adjust the dissolution or dispersion stability of the aqueous resin.

【0021】本発明のインクジェット用記録液には,分
散剤,表面張力,浸透の調整剤,防黴剤,キレート剤,
消泡剤等の添加剤を必要に応じ配合することができる。
分散剤は,顔料の安定な分散を維持させるため,あるい
は水性樹脂を分散剤の用途で使用できない時,あるいは
さらに安定な分散をさせるために用いることができる。
分散剤としては,アニオン性,非イオン性,カチオン
性,両イオン性の活性剤を用いることができる。
The ink-jet recording liquid of the present invention contains a dispersant, a surface tension, an agent for controlling penetration, a fungicide, a chelating agent,
Additives such as an antifoaming agent can be blended as required.
The dispersant can be used to maintain stable dispersion of the pigment, or when the aqueous resin cannot be used for the dispersant, or for more stable dispersion.
Anionic, nonionic, cationic, or zwitterionic activators can be used as the dispersant.

【0022】アニオン性活性剤としては,脂肪酸塩,ア
ルキル硫酸エステル塩,アルキルアリールスルホン酸
塩,アルキルナフタレンスルホン酸塩,ジアルキルスル
ホン酸塩,ジアルキルスルホコハク酸塩,アルキルジア
リールエーテルジスルホン酸塩,アルキルリン酸塩,ポ
リオキシエチレンアルキルエーテル硫酸塩,ポリオキシ
エチレンアルキルアリールエーテル硫酸塩,ナフタレン
スルホン酸フォルマリン縮合物,ポリオキシエチレンア
ルキルリン酸エステル塩,グリセロールボレイト脂肪酸
エステル,ポリオキシエチレングリセロール脂肪酸エス
テル等が例示できる。
Examples of the anionic activator include fatty acid salts, alkyl sulfate salts, alkyl aryl sulfonates, alkyl naphthalene sulfonates, dialkyl sulfonates, dialkyl sulfosuccinates, alkyl diaryl ether disulfonates, and alkyl phosphoric acids. Salt, polyoxyethylene alkyl ether sulfate, polyoxyethylene alkyl aryl ether sulfate, naphthalenesulfonic acid formalin condensate, polyoxyethylene alkyl phosphate ester salt, glycerol borate fatty acid ester, polyoxyethylene glycerol fatty acid ester, etc. Can be illustrated.

【0023】非イオン性活性剤としては,ポリオキシエ
チレンアルキルエーテル,ポリオキシエチレンアルキル
アリールエーテル,ポリオキシエチレンオキシプロピレ
ンブロックコポリマー,ソルビタン脂肪酸エステル,ポ
リオキシエチレンソルビタン脂肪酸エステル,ポリオキ
シエチレンソルビトール脂肪酸エステル,グリセリン脂
肪酸エステル,ポリオキシエチレン脂肪酸エステル,ポ
リオキシエチレンアルキルアミン,フッ素系,シリコン
系等の非イオン性活性剤が例示できる。
Examples of the nonionic activator include polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyoxyethylene oxypropylene block copolymer, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, Examples thereof include glycerin fatty acid ester, polyoxyethylene fatty acid ester, polyoxyethylene alkylamine, fluorine-based, and silicon-based nonionic activators.

【0024】カチオン性活性剤としては,アルキルアミ
ン塩,第4級アンモニウム塩,アルキルピリジニウム
塩,アルキルイミダゾリウム塩等が例示できる。両イオ
ン性活性剤としては,アルキルベタイン,アルキルアミ
ンオキサイド,ホスファジルコリン等が例示できる。
Examples of the cationic activator include an alkylamine salt, a quaternary ammonium salt, an alkylpyridinium salt, an alkylimidazolium salt and the like. Examples of amphoteric surfactants include alkyl betaines, alkylamine oxides, phosphadylcholines, and the like.

【0025】記録液の被印刷体が紙のように浸透性を有
するときには,記録液の浸透をはやめ、見掛けの乾燥性
を早くするため浸透剤を加えることができる。このよう
な浸透剤としては,水性溶剤として例示したジエチレン
グリコールモノブチルエーテル等のグリコールエーテ
ル,アルキレングリコール,アルキレンジオール、ポリ
エチレングリコールモノラウリルエーテル,ラウリル硫
酸ナトリウム,ドデシルベンゼンスルホン酸ナトリウ
ム,オレイン酸ナトリウム,ジオクチルスルホコハク酸
ナトリウム等を用いることができる。浸透剤は,記録液
の5重量%以下の使用量で十分な効果があり,これより
も多いと印字の滲み,紙抜け(プリントスルー)を起こ
し好ましくない。
When the recording liquid is permeable to the printing medium like paper, a penetrant can be added to stop the penetration of the recording liquid and speed up the apparent dryness. Examples of such penetrants include glycol ethers such as diethylene glycol monobutyl ether as exemplified as aqueous solvents, alkylene glycols, alkylene diols, polyethylene glycol monolauryl ether, sodium lauryl sulfate, sodium dodecylbenzenesulfonate, sodium oleate, dioctylsulfosuccinic acid. Sodium or the like can be used. The penetrant has a sufficient effect when used in an amount of 5% by weight or less of the recording liquid, and if it is more than 5% by weight, print bleeding and paper loss (print-through) occur, which is not preferable.

【0026】防黴剤は,記録液への黴や細菌の発生を防
止するために添加することができる。防黴剤としては,
デヒドロ酢酸ナトリウム,安息香酸ナトリウム,ソジウ
ムピリジンチオン−1−オキサイド,ジンクピリジンチ
オン−1−オキサイド,1,2−ベンズイソチアゾリン
−3−オン,1−ベンズイソチアゾリン−3−オンのア
ミン塩等が用いられる。これらは,記録液中に0.05
〜1.0重量%の範囲で含まれることが好ましい。
A fungicide can be added to prevent the generation of mold and bacteria in the recording liquid. As an antifungal agent,
Sodium dehydroacetate, sodium benzoate, sodium pyridinethione-1-oxide, zinc pyridinethione-1-oxide, 1,2-benzisothiazolin-3-one, amine salt of 1-benzisothiazolin-3-one and the like are used. Can be These are 0.05% in the recording solution.
It is preferably contained in the range of 1.0 to 1.0% by weight.

【0027】キレート剤は,記録液中の金属イオンを封
鎖するものであり,ノズル部での金属の析出や記録液中
での不溶解性物の析出等を防止するために加えることが
できる。キレート剤としては,エチレンジアミンテトラ
アセティックアシド,エチレンジアミンテトラアセティ
ックアシドのナトリウム塩,エチレンジアミンテトラア
セティックアシドのジアンモニウム塩,エチレンジアミ
ンテトラアセティックアシドのテトラアンモニウム塩等
が用いられる。これらは,記録液中に0.005〜0.
5重量%の範囲で含まれることが好ましい。
The chelating agent blocks metal ions in the recording liquid, and can be added to prevent deposition of metal at the nozzle portion, precipitation of insoluble substances in the recording liquid, and the like. Examples of the chelating agent include ethylenediaminetetraacetic acid, sodium salts of ethylenediaminetetraacetic acid, diammonium salts of ethylenediaminetetraacetic acid, and tetraammonium salts of ethylenediaminetetraacetic acid. These are contained in the recording liquid in an amount of from 0.005 to 0.
Preferably, it is contained in the range of 5% by weight.

【0028】また,記録液のpHを調整し,記録液の安
定ないし記録装置中の記録液配管との安定性を得るた
め,アミン,無機塩,アンモニア等のpH調整剤,リン
酸等の緩衝液を用いることができる。また,記録液の吐
出時あるいは配管内部での循環,移動,あるいは記録液
の製造時の泡の発生を防止するため消泡剤を添加するこ
ともできる。さらに,顔料の色相の調整,濃度の付与等
を目的として,耐水性,耐光性に問題の無いような形で
染料も使用できる。染料の使用によっては,顔料の分散
安定性を悪くすることもあるので,顔料の40重量%以
下,好ましくは25重量%以下の使用に止める必要があ
る。
Further, in order to adjust the pH of the recording liquid and obtain stability of the recording liquid or stability with the recording liquid piping in the recording apparatus, a pH adjuster such as an amine, an inorganic salt or ammonia, and a buffer such as phosphoric acid. Liquids can be used. Further, an antifoaming agent can be added to prevent the recording liquid from being circulated or moved in the discharge or inside the pipe, or from generating bubbles during the production of the recording liquid. Further, for the purpose of adjusting the hue of the pigment, imparting a concentration, etc., a dye can be used in such a form that there is no problem in water resistance and light resistance. Depending on the use of the dye, the dispersion stability of the pigment may be deteriorated. Therefore, it is necessary to limit the use of the pigment to 40% by weight or less, preferably 25% by weight or less.

【0029】染料としては,分散染料,油溶染料の水不
溶性染料、直接染料,酸性染料,塩基性染料等をレーキ
化により不溶化したもの,反応性染料,含金属染料等が
用いられるが,無機塩の除去された精製染料が好まし
い。染料として具体的には,C.I.ダイレクトブラッ
ク17,19,32,51,71,108,146,1
54,166,C.I.アッドブラック2,7,24,
26,31,52,63,112,118,C.I.ベ
ーシックブラック2,C.I.ダイレクトブルー6,2
2,25,71,90,106,C.I.アシッドブル
ー9,22,40,59,93,102,104,11
3,117,120,167,229,234,C.
I.ベイシックブルー1,3,5,7,9,24,2
5,26,28,29,C.I.ダイレクトレッド1,
4,17,28,83,C.I.アシッドレッド1,
6,32,37,51,52,80,85,87,9
2,94,115,180,256,315,317.
C.I.ベイシックレッド1,2,9,12,13,1
4,37,C.I.ダイレクトエロー12,24,2
6,98,C.I.アシッドエロー11,17,23,
25,29,42,61,71,C.I.ベーシックエ
ロー11,28.C.I.ダイレクトオレンジ34,3
9,44,46,60,C.I.ダイレクトバイオレッ
ト47,48,C.I.ダイレクトブラウン109,
C.I.ダイレクトグリーン59,C.I.アシッドオ
レンジ7,19,C.I.アシッドバイオレット49,
C.I.ベーシックバイオレット7,14,27等が例
示できる。その他の添加剤として,尿素,ジメチル尿素
等を加えることもできる。
Examples of the dye include water-insoluble dyes such as disperse dyes and oil-soluble dyes, direct dyes, acid dyes, basic dyes, and the like, which are made insoluble by lake formation, reactive dyes, metal-containing dyes, and the like. Purified dyes from which salts have been removed are preferred. Specific examples of the dye include C.I. I. Direct Black 17, 19, 32, 51, 71, 108, 146, 1
54, 166, C.I. I. Add Black 2,7,24,
26, 31, 52, 63, 112, 118, C.I. I. Basic Black 2, C.I. I. Direct Blue 6,2
2, 25, 71, 90, 106, C.I. I. Acid Blue 9, 22, 40, 59, 93, 102, 104, 11
3, 117, 120, 167, 229, 234, C.I.
I. Basic Blue 1,3,5,7,9,24,2
5, 26, 28, 29, C.I. I. Direct Red 1,
4, 17, 28, 83, C.I. I. Acid Red 1,
6,32,37,51,52,80,85,87,9
2,94,115,180,256,315,317.
C. I. Basic Red 1,2,9,12,13,1
4, 37, C.I. I. Direct Yellow 12, 24, 2
6,98, C.I. I. Acid Yellow 11, 17, 23,
25, 29, 42, 61, 71, C.I. I. Basic yellow 11, 28. C. I. Direct orange 34,3
9, 44, 46, 60, C.I. I. Direct Violet 47, 48, C.I. I. Direct Brown 109,
C. I. Direct Green 59, C.I. I. Acid Orange 7, 19, C.I. I. Acid violet 49,
C. I. Basic violet 7, 14, 27 and the like can be exemplified. Urea, dimethyl urea and the like can be added as other additives.

【0030】記録液は,記録装置の方式にもよるが,粘
度0.8〜15センチポイズ(25℃)の液体として調
整することが好ましい。記録液の表面張力は25〜60
dyn/cmが好ましく、pHは特に制約されないが4
〜12の範囲であり,処理顔料の分散安定性からは7〜
10のアルカリ性が好ましい。
The recording liquid is preferably adjusted as a liquid having a viscosity of 0.8 to 15 centipoise (25 ° C.), depending on the type of the recording apparatus. The surface tension of the recording liquid is 25-60
dyn / cm is preferable, and the pH is not particularly limited.
To 12 from the dispersion stability of the treated pigment.
An alkalinity of 10 is preferred.

【0031】以下,実施例に基づいて本発明を説明す
る。例中,部および%とあるは,重量部および重量%を
それぞれ示す。 (有機顔料の処理例1〜8)表1に示す条件で,以下の
ように有機顔料を処理した。有機顔料を溶剤に分散さ
せ,加熱したのち,スルホン化剤を添加し,攪拌しなが
ら維持した。ついで,溶剤にて数回洗浄後,水中に注
ぎ,再度水洗を繰り返し,フィルターにて処理顔料の水
性分散体(固形分15%)を得た。
Hereinafter, the present invention will be described with reference to examples. In the examples, parts and% indicate parts by weight and% by weight, respectively. (Process Examples 1 to 8 of Organic Pigment) Under the conditions shown in Table 1, the organic pigment was treated as follows. After the organic pigment was dispersed in the solvent and heated, the sulfonating agent was added and maintained with stirring. Then, after washing several times with a solvent, the mixture was poured into water and washed again with water, and an aqueous dispersion (solid content: 15%) of the treated pigment was obtained with a filter.

【0032】[0032]

【表1】 [Table 1]

【0033】*1 銅フタロシアニンブルー *2 ジメチルキナクリドン *3 キノフタロン *4 N−メチル−2−ピロリドン* 1 Copper phthalocyanine blue * 2 Dimethylquinacridone * 3 Quinophthalone * 4 N-methyl-2-pyrrolidone

【0034】(水性樹脂の合成例)アクリル樹脂の合成
法に従い,メチルメタクリレート(MMA),エチルア
クリレート(EA),メタクリル酸(MAA)を下記の
モノマー組成(モル比)で共重合し,3元共重合体を合
成した。 MMA EA MAA 分子量 合成例1 1 0.5 0.5 10000 2 1 1.0 2.0 20000 3 1 2.0 1.0 20000 4 1 2.0 3.0 25000 5 1 3.0 1.0 28000 6 1 3.0 0.5 18000
(Synthesis example of water-based resin) According to the synthesis method of acrylic resin, methyl methacrylate (MMA), ethyl acrylate (EA), and methacrylic acid (MAA) were copolymerized with the following monomer composition (molar ratio), A copolymer was synthesized. MMA EA MAA molecular weight Synthesis Example 1 10.5 0.5 10000 2 1 1.0 2.0 20,000 3 12.0 1.0 20,000 4 1 2.0 3.0 25000 5 1 3.0 1.0 28000 6 1 3.0 0.5 18000

【0035】(実施例1〜12)サンドミルに,表2に
示す原料を,表2に示す配合比(重量比)で充填し,3
〜4時間の分散を行った。しかるのち,10000rp
mの遠心分離を行い,0.45μのフィルターにて濾過
し,インクジェット用記録液を作製した。
(Examples 1 to 12) The raw materials shown in Table 2 were charged into a sand mill at the compounding ratio (weight ratio) shown in Table 2, and
Dispersion was performed for ~ 4 hours. After a while, 10,000 rpm
m, and the mixture was filtered through a 0.45 μ filter to prepare an inkjet recording liquid.

【0036】[0036]

【表2】 [Table 2]

【0037】分散剤1 花王社製ノニオン系活性剤「エ
マルゲン420 」 分散剤2 花王社製ノニオン系活性剤「エマルゲンA-9
0」 分散剤3 ゼネカ社製ノニオン系分散剤「ソルスパース
27000 」 アクリル樹脂1 日本ポリマー社製アクリル樹脂エマル
ション「W−251」固形分40% アクリル樹脂2 岐阜シェラック社製アクリル樹脂エマ
ルション「エマポリーTYN−50」、固形分44% アクリル樹脂3 ジョンソンポリマー社製アクリル樹脂
水溶液「ジョンクリル62」、固形分31% アクリル樹脂4 ジョンソンポリマー社製アクリル樹脂
水溶液「ジョンクリル61J」、固形分31%
Dispersant 1 Nonionic activator "Emulgen 420" manufactured by Kao Corporation Dispersant 2 Nonionic activator "Emulgen A-9" manufactured by Kao Corporation
0 "Dispersant 3 Nonionic dispersant" SOLSPERS
27000 "Acrylic resin 1 Acrylic resin emulsion" W-251 "manufactured by Nippon Polymer Co., Ltd. 40% solid content Acrylic resin 2 Acrylic resin emulsion" Emapoly TYN-50 "manufactured by Gifu Shellac, 44% solid content Acrylic resin 3 Acrylic resin manufactured by Johnson Polymer Aqueous resin solution “Johncryl 62”, solid content 31% Acrylic resin 4 Acrylic resin aqueous solution “Johncryl 61J” manufactured by Johnson Polymer, solid content 31%

【0038】中和剤1 ジメチルアミノエタノール 中和剤2 ジエチルアミノエタノール 中和剤3 モノエタノールアミン 湿潤剤1 グリセリン 湿潤剤2 エチレングリコール 溶剤1 イソプロピルアルコール 溶剤2 エチルアルコール 溶剤3 N−メチル−2−ピロリドン 防黴剤1 ゼネカ社製「プロクセルGXL 」 防黴剤2 オーリン社製「ソジウムオマジン」 キレート剤 エチレンジアミンテトラアセティックアシ
ドナトリウム塩
Neutralizer 1 Dimethylaminoethanol Neutralizer 2 Diethylaminoethanol Neutralizer 3 Monoethanolamine Wetting agent 1 Glycerin Wetting agent 2 Ethylene glycol Solvent 1 Isopropyl alcohol Solvent 2 Ethyl alcohol Solvent 3 N-methyl-2-pyrrolidone Fungicide 1 "Proxel GXL" manufactured by Zeneca Corp. Antifungal 2 "Sodium Omazine" manufactured by Ohlin Chelating agent Sodium ethylenediaminetetraacetic acid

【0039】実施例で得られた記録液について、下記の
方法で分散性を評価した。また、実施例で得られた記録
液をインクジェットプリンター(エプソン社製「MJ7
00V2C」)のカートリッジに入れて記録を行い,記
録物の耐水性,耐摩擦性,耐光性を下記の方法で評価し
た。結果を表3に示す。さらに、実施例で得られた記録
液を−40℃で一週間保存後,自然解凍したところ、初
期の粘度を維持しており,安定な噴射特性を示した。ま
た,50℃の恒温槽で1月保存したところ,初期の粘度
を維持しており,安定な噴射特性を示した。また,−4
0℃7時間,室温7時間,50℃7時間のサイクルを3
回繰り返して行ったところ,初期の印字特性および記録
液の物性値を維持していた。
The recording liquid obtained in the examples was evaluated for dispersibility by the following method. Further, the recording liquid obtained in the examples was applied to an ink jet printer (“MJ7” manufactured by Epson Corporation).
00V2C ”), and recording was performed, and the water resistance, friction resistance, and light resistance of the recorded matter were evaluated by the following methods. Table 3 shows the results. Further, when the recording liquid obtained in the example was stored at -40 ° C for one week and then naturally thawed, the initial viscosity was maintained and stable ejection characteristics were exhibited. When stored in a 50 ° C constant temperature bath for one month, the initial viscosity was maintained and stable injection characteristics were exhibited. Also, -4
A cycle of 7 hours at 0 ° C, 7 hours at room temperature, and 7 hours at 50 ° C
When the printing was repeated several times, the initial printing characteristics and the physical properties of the recording liquid were maintained.

【0040】耐水性 コピー用紙「Xerox402
4」に印字,6時間放置後,水道水中に5分浸漬し,試
験前後のOD値を測定し,残存した率を示した。 耐摩擦性 アート紙にベタ印字した記録物を湿った綿棒
にて3回こすったときの印字部の変化を目視にて評価し
た。 耐光性 塗工合成紙に印字ラミネート後,フェードメ
ーターで500時間曝露し,曝露前後の色差を求めた。 分散性 記録液を50℃7日間保存後の粒子径の変化
を測定した。 良 :15nm未満の変化 不良:15nm以上の変化
Water-resistant copy paper "Xerox 402"
No. 4 ", left for 6 hours, immersed in tap water for 5 minutes, measured the OD value before and after the test, and showed the percentage remaining. Abrasion Resistance The change in the printed area when the solid printed on the art paper was rubbed three times with a wet cotton swab was visually evaluated. Lightfastness After printing and laminating on the coated synthetic paper, it was exposed for 500 hours with a fade meter, and the color difference before and after exposure was determined. Dispersibility A change in the particle size of the recording liquid after storage at 50 ° C. for 7 days was measured. Good: Change of less than 15 nm Bad: Change of 15 nm or more

【0041】 [0041]

【0042】[0042]

【発明の効果】本発明の記録液は,顔料を水性の液体に
分散した水分散型のインクジェット用記録液でありなが
ら,分散性が安定しており,ノズルでの吐出安定性が良
好なため,オフィスにおける書類の作成,ダンボールの
マーキング,ナンバリング,バーコード等の分野,オン
デマンド印刷,簡易印刷の分野にて利用することができ
る。
The recording liquid of the present invention is a water-dispersion type ink-jet recording liquid in which a pigment is dispersed in an aqueous liquid, but has a stable dispersibility and a good discharge stability at a nozzle. It can be used in the fields of office document creation, cardboard marking, numbering, barcode, etc., on-demand printing, and simple printing.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 飯田 保春 東京都中央区京橋二丁目3番13号東洋イン キ製造株式会社内 ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Yasuharu Iida 2-3-13-1 Kyobashi, Chuo-ku, Tokyo Toyo Inki Manufacturing Co., Ltd.

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】水性の液体中に有機顔料を分散してなるイ
ンクジェット用記録液において,該有機顔料が,スルホ
ン酸との反応性を有さない溶剤中に有機顔料を分散し,
しかるのちスルホン化剤により処理した処理顔料である
ことを特徴とするインクジェット用記録液。
1. An ink jet recording liquid comprising an organic pigment dispersed in an aqueous liquid, wherein the organic pigment is dispersed in a solvent having no reactivity with sulfonic acid.
A recording liquid for ink jet, which is a treated pigment which has been treated with a sulfonating agent.
【請求項2】水性の液体中に有機顔料を分散してなるイ
ンクジェット用記録液において,該有機顔料が,顔料の
粒子内部に実質的にスルホン酸基を有さず,顔料の粒子
表面にスルホン酸基を有する処理顔料であることを特徴
とするインクジェット用記録液。
2. An ink jet recording liquid comprising an organic pigment dispersed in an aqueous liquid, wherein the organic pigment has substantially no sulfonic acid group inside the pigment particles, An inkjet recording liquid, which is a treated pigment having an acid group.
【請求項3】スルホン酸との反応性を有さない溶剤が,
活性プロトンを有さないことを特徴とする請求項1また
は2記載のインクジェット用記録液。
3. A solvent having no reactivity with sulfonic acid,
3. The ink jet recording liquid according to claim 1, having no active proton.
【請求項4】スルホン酸との反応性を有さない溶剤が,
N−メチル−2−ピロリドンまたはスルホランであるこ
とを特徴とする請求項1または2記載のインクジェト用
記録液。
4. A solvent having no reactivity with sulfonic acid,
3. The ink jet recording liquid according to claim 1, which is N-methyl-2-pyrrolidone or sulfolane.
【請求項5】スルホン化剤が,スルホン化ピリジン塩ま
たはスルファミン酸であることを特徴とする請求項1な
いし4いずれか1項に記載のインクジェット用記録液。
5. The ink-jet recording liquid according to claim 1, wherein the sulfonating agent is a sulfonated pyridine salt or sulfamic acid.
【請求項6】処理顔料のレーザ散乱法により測定した平
均粒径が10〜150nmであることを特徴とする請求
項1ないし5いずれか1項に記載のインクジェット用記
録液。
6. An ink jet recording liquid according to claim 1, wherein the treated pigment has an average particle diameter of 10 to 150 nm as measured by a laser scattering method.
【請求項7】処理顔料を固形分で0.1〜10重量%含
むことを特徴とする請求項1ないし6いずれか1項に記
載のインクジェット用記録液。
7. The ink-jet recording liquid according to claim 1, wherein the treated pigment contains 0.1 to 10% by weight as a solid content.
JP26571996A 1996-10-07 1996-10-07 Inkjet recording liquid Expired - Fee Related JP3141792B2 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP26571996A JP3141792B2 (en) 1996-10-07 1996-10-07 Inkjet recording liquid
US08/944,437 US5928419A (en) 1996-10-07 1997-10-06 Surface-treated organic pigment and process for the production thereof
DE69709015T DE69709015T2 (en) 1996-10-07 1997-10-07 Surface-treated organic pigment and process for its production
DE69710878T DE69710878T2 (en) 1996-10-07 1997-10-07 Ink jet recording liquid containing a surface-treated organic pigment
EP98119588A EP0894835B1 (en) 1996-10-07 1997-10-07 Inkjet recording liquid comprising a surface-treated organic pigment
EP97307934A EP0834537B1 (en) 1996-10-07 1997-10-07 Surface-treated organic pigment and process for the production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26571996A JP3141792B2 (en) 1996-10-07 1996-10-07 Inkjet recording liquid

Publications (2)

Publication Number Publication Date
JPH10110129A true JPH10110129A (en) 1998-04-28
JP3141792B2 JP3141792B2 (en) 2001-03-05

Family

ID=17421067

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26571996A Expired - Fee Related JP3141792B2 (en) 1996-10-07 1996-10-07 Inkjet recording liquid

Country Status (1)

Country Link
JP (1) JP3141792B2 (en)

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002338843A (en) * 2001-05-08 2002-11-27 Hewlett Packard Co <Hp> Solubilization of pigment by treatment with strong base and replacement
US6599356B2 (en) 2000-06-28 2003-07-29 Seiko Epson Corporation Method for manufacturing pigment dispersed liquid, and pigment dispersed liquid, and ink for ink-jet printer recording using said pigment dispersed liquid
EP1146090A3 (en) * 2000-04-10 2004-01-28 Seiko Epson Corporation Process for the preparation of pigment dispersion, pigment dispersion obtained by the same, ink jet recording ink comprising the same, and recording method and recording material using the same
US6802893B1 (en) 1999-06-09 2004-10-12 Seiko Epson Corporation Ink for ink-jet recording and process for producing the same, ink set for ink-jet recording, and ink cartridge
US6902250B2 (en) 2002-05-29 2005-06-07 Fuji Xerox Co., Ltd. Ink-jet recording method and ink-jet recording apparatus for displacing recording head from printing position when printing is being stopped
US7001935B2 (en) 2001-03-12 2006-02-21 Seiko Epson Corporation Ink for ink jet printing process and printed matter obtained using the same
US7063415B2 (en) 1998-07-21 2006-06-20 Ricoh Company, Ltd. Liquid jet apparatus using a fine particle dispersion liquid composition
US7074843B2 (en) 2001-08-27 2006-07-11 Seiko Epson Corporation Microencapsulated pigment, production process therefor, aqueous dispersion and ink jet recording ink
US7253216B2 (en) 2002-09-30 2007-08-07 Seiko Epson Corporation Microencapsulated pigment, production process therefor, and aqueous dispersion and ink jet recording ink using the pigment
US7423076B2 (en) 2003-10-14 2008-09-09 Seiko Epson Corporation Microencapsulated pigment, preparation process therefor, aqueous dispersion and ink jet recording ink
EP1967375A2 (en) 2007-03-08 2008-09-10 Konica Minolta Holdings, Inc. Ink-Jet Recording Method and Ink-Jet Recording Apparatus
EP1975214A1 (en) 2007-03-29 2008-10-01 Konica Minolta Holdings, Inc. Ink-jet ink and ink-jet recording method
WO2009060632A1 (en) 2007-11-06 2009-05-14 Konica Minolta Ij Technologies, Inc. Nonaqueous jet printing ink and method of ink-jet recording
EP2075293A1 (en) 2007-12-28 2009-07-01 Konica Minolta Holdings, Inc. Ink-jet ink and ink-jet recording method
WO2009123008A1 (en) 2008-04-04 2009-10-08 コニカミノルタIj株式会社 Nonaqueous ink jet ink, process for producing nonaqueous ink jet ink, and ink jet recording method
EP2145932A1 (en) 2008-07-16 2010-01-20 Fujifilm Corporation Aqueous ink composition, aqueous ink composition for inkjet recording, and inkjet recording method
WO2010041707A1 (en) 2008-10-08 2010-04-15 理想科学工業株式会社 Aqueous inkjet ink
EP2423276A1 (en) 2010-08-24 2012-02-29 Fujifilm Corporation Aqueous ink composition, inkjet recording method, and inkjet printed article
WO2012096138A1 (en) 2011-01-12 2012-07-19 富士フイルム株式会社 Ink composition, image forming method, and print
EP2492322A1 (en) 2011-02-23 2012-08-29 Fujifilm Corporation Ink composition, image forming method, and printed material
EP2500387A1 (en) 2011-03-15 2012-09-19 Fujifilm Corporation Ink composition, image forming method, and print material
WO2012124790A1 (en) 2011-03-14 2012-09-20 Ricoh Company, Ltd. Inkjet ink, inkjet recording method, and inkjet recording device
WO2012176915A1 (en) 2011-06-24 2012-12-27 Fujifilm Corporation Ink composition, image forming method and printed material
EP2559741A2 (en) 2011-08-15 2013-02-20 Fujifilm Corporation Ink composition, image forming method, and printed material
WO2013114929A1 (en) 2012-02-01 2013-08-08 富士フイルム株式会社 Water-based ink composition and image formation method
EP2626390A2 (en) 2012-02-13 2013-08-14 Fujifilm Corporation Ink composition and image forming method
EP2626392A1 (en) 2012-02-13 2013-08-14 Fujifilm Corporation Ink composition, image forming method, and printed article using the same
US8524803B2 (en) 2004-10-18 2013-09-03 Seiko Epson Corporation Encapsulation product, process for producing the same, and ink composition
EP2644404A2 (en) 2012-03-28 2013-10-02 FUJIFILM Corporation Ink composition, image forming method, and printed article
WO2014030515A1 (en) 2012-08-22 2014-02-27 富士フイルム株式会社 Ink composition, image formation method, and printed matter
WO2014030473A1 (en) 2012-08-23 2014-02-27 富士フイルム株式会社 Ink composition, image forming method, printed matter, and graft copolymer
WO2014136924A1 (en) 2013-03-08 2014-09-12 富士フイルム株式会社 Multilayer structure, multilayer structure manufacturing method and composition set
EP2781565A1 (en) 2013-03-22 2014-09-24 Fujifilm Corporation White ink composition, ink set for forming multiple layers, image forming method and printed matter
WO2014157130A1 (en) 2013-03-26 2014-10-02 富士フイルム株式会社 Inkjet recording method, printing substance, and ink set
EP2796518A1 (en) 2013-03-04 2014-10-29 Fujifilm Corporation Process for producing decorative sheet, decorative sheet, decorative sheet molded product, process for producing in-mold molded article, and in-mold molded article
US9010917B2 (en) 2012-05-30 2015-04-21 Ricoh Company, Ltd. Inkjet recording method and inkjet printed matter
US10678156B2 (en) 2017-03-27 2020-06-09 Canon Kabushiki Kaisha Pigment dispersion, method for manufacturing toner, aqueous ink, and triazo compound

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS504019B1 (en) * 1969-11-15 1975-02-13
JPS5318630A (en) * 1976-08-05 1978-02-21 Basf Ag Phthalocyanine preparations easily dispersible in water
JPH03210375A (en) * 1989-11-28 1991-09-13 Ciba Geigy Ag New water paint compound containing specially modified organic pigments
JPH04227669A (en) * 1990-04-12 1992-08-17 Hewlett Packard Co <Hp> Ink composition
JPH05186704A (en) * 1992-01-13 1993-07-27 Tokai Carbon Co Ltd Surface-modified carbon black and production thereof
JPH05247391A (en) * 1992-03-09 1993-09-24 Citizen Watch Co Ltd Recording liquid
JPH06145545A (en) * 1992-11-12 1994-05-24 Ricoh Co Ltd Ink jet recording ink
JPH08157759A (en) * 1994-12-02 1996-06-18 Kao Corp Water-base ink for ink jet recording
JPH08283596A (en) * 1995-04-14 1996-10-29 Toyo Ink Mfg Co Ltd Surface-treated pigment and its manufacture
JPH0940898A (en) * 1995-07-26 1997-02-10 Hitachi Maxell Ltd Ultrafine particle organic pigment ink and its production
JPH09208849A (en) * 1996-01-31 1997-08-12 Bayer Corp Water-based coating containing phthalocyanine
JPH1053716A (en) * 1996-04-24 1998-02-24 Hoechst Ag Surface-treated quinacridone or dioxazine pigment
JPH10110110A (en) * 1996-10-07 1998-04-28 Toyo Ink Mfg Co Ltd Surface-treated pigment and its production
JPH10110112A (en) * 1996-10-07 1998-04-28 Toyo Ink Mfg Co Ltd Surface-treated carbon black and its production
JPH10110111A (en) * 1996-10-07 1998-04-28 Toyo Ink Mfg Co Ltd Surface-treated pigment and its production
JPH10110127A (en) * 1996-10-09 1998-04-28 Toyo Ink Mfg Co Ltd Recording solution for ink-jet

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS504019B1 (en) * 1969-11-15 1975-02-13
JPS5318630A (en) * 1976-08-05 1978-02-21 Basf Ag Phthalocyanine preparations easily dispersible in water
JPH03210375A (en) * 1989-11-28 1991-09-13 Ciba Geigy Ag New water paint compound containing specially modified organic pigments
JPH04227669A (en) * 1990-04-12 1992-08-17 Hewlett Packard Co <Hp> Ink composition
JPH05186704A (en) * 1992-01-13 1993-07-27 Tokai Carbon Co Ltd Surface-modified carbon black and production thereof
JPH05247391A (en) * 1992-03-09 1993-09-24 Citizen Watch Co Ltd Recording liquid
JPH06145545A (en) * 1992-11-12 1994-05-24 Ricoh Co Ltd Ink jet recording ink
JPH08157759A (en) * 1994-12-02 1996-06-18 Kao Corp Water-base ink for ink jet recording
JPH08283596A (en) * 1995-04-14 1996-10-29 Toyo Ink Mfg Co Ltd Surface-treated pigment and its manufacture
JPH0940898A (en) * 1995-07-26 1997-02-10 Hitachi Maxell Ltd Ultrafine particle organic pigment ink and its production
JPH09208849A (en) * 1996-01-31 1997-08-12 Bayer Corp Water-based coating containing phthalocyanine
JPH1053716A (en) * 1996-04-24 1998-02-24 Hoechst Ag Surface-treated quinacridone or dioxazine pigment
JPH10110110A (en) * 1996-10-07 1998-04-28 Toyo Ink Mfg Co Ltd Surface-treated pigment and its production
JPH10110112A (en) * 1996-10-07 1998-04-28 Toyo Ink Mfg Co Ltd Surface-treated carbon black and its production
JPH10110111A (en) * 1996-10-07 1998-04-28 Toyo Ink Mfg Co Ltd Surface-treated pigment and its production
JPH10110127A (en) * 1996-10-09 1998-04-28 Toyo Ink Mfg Co Ltd Recording solution for ink-jet

Cited By (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7178912B2 (en) 1998-07-21 2007-02-20 Ricoh Company, Ltd. Liquid jet apparatus using a fine particle dispersion liquid composition
US7578577B2 (en) 1998-07-21 2009-08-25 Ricoh Company, Ltd. Liquid jet apparatus using a fine particle dispersion liquid composition
US7578575B2 (en) 1998-07-21 2009-08-25 Ricoh Company, Ltd. Liquid jet apparatus using a fine particle dispersion liquid composition
US7063415B2 (en) 1998-07-21 2006-06-20 Ricoh Company, Ltd. Liquid jet apparatus using a fine particle dispersion liquid composition
US6802893B1 (en) 1999-06-09 2004-10-12 Seiko Epson Corporation Ink for ink-jet recording and process for producing the same, ink set for ink-jet recording, and ink cartridge
EP1669425A1 (en) 1999-06-09 2006-06-14 Seiko Epson Corporation Ink for ink jet recording with antifungal additive
EP1146090A3 (en) * 2000-04-10 2004-01-28 Seiko Epson Corporation Process for the preparation of pigment dispersion, pigment dispersion obtained by the same, ink jet recording ink comprising the same, and recording method and recording material using the same
US6916862B2 (en) 2000-04-10 2005-07-12 Seiko Epson Corporation Process for the preparation of pigment dispersion, pigment dispersion obtained by the same, ink jet recording ink comprising the same, and recording method and recorded material using the same
US6599356B2 (en) 2000-06-28 2003-07-29 Seiko Epson Corporation Method for manufacturing pigment dispersed liquid, and pigment dispersed liquid, and ink for ink-jet printer recording using said pigment dispersed liquid
US7001935B2 (en) 2001-03-12 2006-02-21 Seiko Epson Corporation Ink for ink jet printing process and printed matter obtained using the same
JP2002338843A (en) * 2001-05-08 2002-11-27 Hewlett Packard Co <Hp> Solubilization of pigment by treatment with strong base and replacement
JP4593058B2 (en) * 2001-05-08 2010-12-08 ヒューレット・パッカード・カンパニー Solubilization of pigments by treatment and substitution with strong bases.
US7074843B2 (en) 2001-08-27 2006-07-11 Seiko Epson Corporation Microencapsulated pigment, production process therefor, aqueous dispersion and ink jet recording ink
US7683108B2 (en) 2001-08-27 2010-03-23 Seiko Epson Corporation Microencapsulated pigment, production process therefor, aqueous dispersion, and ink jet recording ink
US6902250B2 (en) 2002-05-29 2005-06-07 Fuji Xerox Co., Ltd. Ink-jet recording method and ink-jet recording apparatus for displacing recording head from printing position when printing is being stopped
US7253216B2 (en) 2002-09-30 2007-08-07 Seiko Epson Corporation Microencapsulated pigment, production process therefor, and aqueous dispersion and ink jet recording ink using the pigment
US7423076B2 (en) 2003-10-14 2008-09-09 Seiko Epson Corporation Microencapsulated pigment, preparation process therefor, aqueous dispersion and ink jet recording ink
US7812070B2 (en) 2003-10-14 2010-10-12 Seiko Epson Corporation Microencapsulated pigment, preparation process therefor, aqueous dispersion and ink jet recording ink
US8524803B2 (en) 2004-10-18 2013-09-03 Seiko Epson Corporation Encapsulation product, process for producing the same, and ink composition
EP1967375A2 (en) 2007-03-08 2008-09-10 Konica Minolta Holdings, Inc. Ink-Jet Recording Method and Ink-Jet Recording Apparatus
EP1975214A1 (en) 2007-03-29 2008-10-01 Konica Minolta Holdings, Inc. Ink-jet ink and ink-jet recording method
WO2009060632A1 (en) 2007-11-06 2009-05-14 Konica Minolta Ij Technologies, Inc. Nonaqueous jet printing ink and method of ink-jet recording
EP2075293A1 (en) 2007-12-28 2009-07-01 Konica Minolta Holdings, Inc. Ink-jet ink and ink-jet recording method
WO2009123008A1 (en) 2008-04-04 2009-10-08 コニカミノルタIj株式会社 Nonaqueous ink jet ink, process for producing nonaqueous ink jet ink, and ink jet recording method
EP2145932A1 (en) 2008-07-16 2010-01-20 Fujifilm Corporation Aqueous ink composition, aqueous ink composition for inkjet recording, and inkjet recording method
WO2010041707A1 (en) 2008-10-08 2010-04-15 理想科学工業株式会社 Aqueous inkjet ink
EP2423276A1 (en) 2010-08-24 2012-02-29 Fujifilm Corporation Aqueous ink composition, inkjet recording method, and inkjet printed article
WO2012096138A1 (en) 2011-01-12 2012-07-19 富士フイルム株式会社 Ink composition, image forming method, and print
EP2492322A1 (en) 2011-02-23 2012-08-29 Fujifilm Corporation Ink composition, image forming method, and printed material
WO2012124790A1 (en) 2011-03-14 2012-09-20 Ricoh Company, Ltd. Inkjet ink, inkjet recording method, and inkjet recording device
EP2500387A1 (en) 2011-03-15 2012-09-19 Fujifilm Corporation Ink composition, image forming method, and print material
WO2012176915A1 (en) 2011-06-24 2012-12-27 Fujifilm Corporation Ink composition, image forming method and printed material
EP2559741A2 (en) 2011-08-15 2013-02-20 Fujifilm Corporation Ink composition, image forming method, and printed material
WO2013114929A1 (en) 2012-02-01 2013-08-08 富士フイルム株式会社 Water-based ink composition and image formation method
EP2626392A1 (en) 2012-02-13 2013-08-14 Fujifilm Corporation Ink composition, image forming method, and printed article using the same
EP2626390A2 (en) 2012-02-13 2013-08-14 Fujifilm Corporation Ink composition and image forming method
EP2644404A2 (en) 2012-03-28 2013-10-02 FUJIFILM Corporation Ink composition, image forming method, and printed article
US9010917B2 (en) 2012-05-30 2015-04-21 Ricoh Company, Ltd. Inkjet recording method and inkjet printed matter
WO2014030515A1 (en) 2012-08-22 2014-02-27 富士フイルム株式会社 Ink composition, image formation method, and printed matter
WO2014030473A1 (en) 2012-08-23 2014-02-27 富士フイルム株式会社 Ink composition, image forming method, printed matter, and graft copolymer
EP2796518A1 (en) 2013-03-04 2014-10-29 Fujifilm Corporation Process for producing decorative sheet, decorative sheet, decorative sheet molded product, process for producing in-mold molded article, and in-mold molded article
WO2014136924A1 (en) 2013-03-08 2014-09-12 富士フイルム株式会社 Multilayer structure, multilayer structure manufacturing method and composition set
EP2781565A1 (en) 2013-03-22 2014-09-24 Fujifilm Corporation White ink composition, ink set for forming multiple layers, image forming method and printed matter
WO2014157130A1 (en) 2013-03-26 2014-10-02 富士フイルム株式会社 Inkjet recording method, printing substance, and ink set
US10678156B2 (en) 2017-03-27 2020-06-09 Canon Kabushiki Kaisha Pigment dispersion, method for manufacturing toner, aqueous ink, and triazo compound

Also Published As

Publication number Publication date
JP3141792B2 (en) 2001-03-05

Similar Documents

Publication Publication Date Title
JP3141792B2 (en) Inkjet recording liquid
JP3301295B2 (en) Method for producing finely divided pigment
JP4752034B2 (en) Inkjet recording liquid and recording method using the same
WO1997031072A1 (en) Water-based ink-jet recording fluid
JPH11246807A (en) Waterborne pigment dispersion and recording solution for ink jetting
JP3817790B2 (en) Inkjet recording fluid
JP3317162B2 (en) Inkjet recording liquid
JPH09227812A (en) Water-base ink jet recording liquid
JP2001139863A (en) Method for manufacturing recording liquid for ink jet recording
JP3493867B2 (en) Recording liquid for inkjet
JP3206457B2 (en) Inkjet ink and inkjet ink set
JP3499953B2 (en) Ink jet ink and method for producing the same
JPH1081843A (en) Ink jet ink and ink jet ink set
JP2002220557A (en) Process printing ink set
JP3812002B2 (en) Inkjet recording fluid
JPH0953035A (en) Ink jet recording fluid and its production
JP3491428B2 (en) Inkjet recording liquid and method for producing the same
JP3706477B2 (en) Inkjet ink manufacturing method
JPH09221616A (en) Recording liquid for ink-jet recording and its production
JP3521594B2 (en) Recording liquid for inkjet
JP3470484B2 (en) Ink jet recording liquid and method for producing the same
JPH0953036A (en) Ink jet recording fluid and its production
JP2005082663A (en) Ink composition
JPH10219165A (en) Ink jet recording fluid
JP3487058B2 (en) Inkjet recording liquid and method for producing the same

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees