JPS60124670A - Ink - Google Patents

Ink

Info

Publication number
JPS60124670A
JPS60124670A JP58232926A JP23292683A JPS60124670A JP S60124670 A JPS60124670 A JP S60124670A JP 58232926 A JP58232926 A JP 58232926A JP 23292683 A JP23292683 A JP 23292683A JP S60124670 A JPS60124670 A JP S60124670A
Authority
JP
Japan
Prior art keywords
compd
dye
ink
water
formula
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
JP58232926A
Other languages
Japanese (ja)
Other versions
JPH0142308B2 (en
Inventor
Kazuhiro Sugimoto
杉本 和宥
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.)
SHIYACHIHATA KOGYO KK
Shachihata Industry Co Ltd
Original Assignee
SHIYACHIHATA KOGYO KK
Shachihata Industry 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 SHIYACHIHATA KOGYO KK, Shachihata Industry Co Ltd filed Critical SHIYACHIHATA KOGYO KK
Priority to JP58232926A priority Critical patent/JPS60124670A/en
Publication of JPS60124670A publication Critical patent/JPS60124670A/en
Publication of JPH0142308B2 publication Critical patent/JPH0142308B2/ja
Granted legal-status Critical Current

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  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

PURPOSE:To provide a water ink which has excellent long-term stability, water resistance, dye developability and dry resistance when left standing in air over a long period of time, by blending a specified tert, amine compd. or a triazine derivative with an aq. soln. of a water-soluble dye. CONSTITUTION:A compd. of formula I (wherein 1<=a<=5; 1<=b<=5; 1<=c<=5) or a compd. of formula II (wherein 1<=n<=5) and optionally a solvent such as polyhydric alcohol, glycol, or glycol ether, a preservative, etc. are blended with an aq. soln. of a dye such as a water-soluble acid dye, direct dye or basic dye to obtain the desired ink. An example of the compd. of formula I is a compd. of formula III. An example of the compd. of formula II is a compd. of formula IV. These compds. are used in a quantity of pref. 0.5-3wt% based on that of the ink.

Description

【発明の詳細な説明】 ンキに関するもので、さらに詳細には経時安定性、耐水
性がよく、染料の発色性向上、及び長期間大気中に放置
しても耐乾燥性(蒸発安定性)に優れた水性インキに関
する。
[Detailed Description of the Invention] It relates to ink, and more specifically, it has good stability over time, good water resistance, improved color development of the dye, and good drying resistance (evaporation stability) even when left in the air for a long period of time. Regarding excellent water-based inks.

従来の筆記具用インキは筆記具のキャップ外し長期間大
気中に放置するとペン先部に染料が析出し、カスしたり
、変色したり、筆記できな(なる等の欠点があった。又
従来のスタンプ台は蓋を開いたまま放置すると盤面に染
料等が析出し捺印ムラ、変色等の欠点があった。本発明
はこれらの欠点を解消し経時安定性、耐乾燥性、耐水性
に優れたインキを提供するものである。
Conventional ink for writing instruments has disadvantages such as when the cap of the writing instrument is removed and left in the air for a long period of time, the dye precipitates on the tip of the pen, causing scum, discoloration, and the inability to write. If the stand is left with its lid open, dyes, etc. will precipitate on the surface of the board, resulting in uneven printing and discoloration.The present invention solves these shortcomings and provides an ink with excellent stability over time, dryness resistance, and water resistance. It provides:

即ち、本発明は水溶性染料の水溶液に下記一般式よりな
る(A)又は(B)を配合したことを特徴とするインキ
を要旨とするものである。
That is, the gist of the present invention is an ink characterized by blending (A) or (B) represented by the following general formula into an aqueous solution of a water-soluble dye.

次に本発明の水性インキの各成分について詳細に説明す
る。
Next, each component of the water-based ink of the present invention will be explained in detail.

水溶性染料としては、水溶性の酸性染料、直接染料、塩
基性染料等の染料が使用できる。
As the water-soluble dye, dyes such as water-soluble acid dyes, direct dyes, and basic dyes can be used.

例えば、酸性染料としては、C1,Ac1d Oren
ge (C1,15575) 、C1,Ac1d Re
d27 (C1,16185)、C1,Ac1d Bl
ue93 (C1,42780) 、直接染料としては
、Direct Fast BIackD (C1,2
7700)、C1,Direct BIack19(C
1,35255)、Direct Sky B1ue6
B (C1,24410) 、塩基性染料としては、C
I 、 Ba5ic Red 1 (C1,45160
) 、C1,Ba5ic Blue 7 (C1,42
595)、CI Ba5ic Yellow 2 (C
1,41000)、これらを単独或いは他の水溶性染料
との組合せにより使用される。これらの染料は目的に応
じ変更されるがインキの2%〜30%(重量)使用スる
場合に最も良好な結果かえられる。
For example, acid dyes include C1, Ac1d Oren
ge (C1, 15575), C1, Ac1d Re
d27 (C1, 16185), C1, Ac1d Bl
ue93 (C1,42780), Direct Fast BIackD (C1,2
7700), C1, Direct BIack19 (C
1,35255), Direct Sky B1ue6
B (C1,24410), as a basic dye, C
I, Ba5ic Red 1 (C1,45160
), C1,Ba5ic Blue 7 (C1,42
595), CI Ba5ic Yellow 2 (C
1,41,000), these can be used alone or in combination with other water-soluble dyes. These dyes may be varied depending on the purpose, but best results are obtained when they are used in an amount of 2% to 30% (by weight) of the ink.

次に、前記一般式(A)及び(B)で示した化合物は使
用される目的に応じ変更されるが、インキの0.5%〜
3.0%(重量)使用する場合が最も良好な結果かえら
れる。前記一般式(A)及び(B)で示した化合物の添
加による効果は次の通りである。
Next, the compounds represented by the general formulas (A) and (B) are changed depending on the purpose of use, but 0.5% to
The best results can be obtained when using 3.0% (by weight). The effects of adding the compounds represented by the general formulas (A) and (B) are as follows.

染料の溶解度をアップできるため、今まで使用しにくか
った染料(特に直接染料)を使用可能にし、耐水性の良
いインキが得られる。又、染料の発色性を良くしかつ、
高沸点化合物であるためインキの蒸発を防止すると共に
染料の析出を無くし、経時安定性の良い、耐乾燥性に優
れたインキかえられる。
Since the solubility of dyes can be increased, dyes that were previously difficult to use (especially direct dyes) can now be used, and ink with good water resistance can be obtained. In addition, it improves the color development of the dye and
Since it is a high boiling point compound, it prevents ink evaporation and eliminates dye precipitation, making it possible to replace ink with good stability over time and excellent drying resistance.

又必要に応じて、多価アルコール系熔剤、グリコール系
熔剤、グリコールエーテル系溶剤等の溶剤および、防腐
剤、防黴剤、界面活性剤等を適宜使用することもできる
。以下実施例にて説明する。
Further, if necessary, solvents such as polyhydric alcohol-based melts, glycol-based melts, and glycol ether-based solvents, as well as preservatives, antifungal agents, surfactants, and the like can be used as appropriate. This will be explained below using examples.

実施例1筆記具用インキ (単位は重量部)・C1,D
irect Black19 1fi(C1,3525
5) ・水 50 (一般式中a=b=c=l) CI、CI−1,OH 1 (一般式中n−1) ・チオジグリコール 2.5 ・フェノール 0.5 ・エチレングリコール 20 ・ジエチレングリコール 10 上記水と化合物(A)及び(B)及びエチレングリコル
とジエチレングリコールを混合し、染料を完全に熔解し
、次いで残りの成分を添加混合攪拌し黒インキを得た。
Example 1 Ink for writing instruments (unit: parts by weight)・C1,D
direct Black19 1fi(C1,3525
5) - Water 50 (a=b=c=l in the general formula) CI, CI-1, OH 1 (n-1 in the general formula) - Thiodiglycol 2.5 - Phenol 0.5 - Ethylene glycol 20 - Diethylene glycol 10 The above water, compounds (A) and (B), and ethylene glycol and diethylene glycol were mixed to completely dissolve the dye, and then the remaining components were added, mixed and stirred to obtain a black ink.

実施例2スタンプインキ ・C1,Direct B1ack51 20(C1,
27720) ・グリセリン 56 ・水 20 ドデシルベンゼンスルホン酸ソーダ 1(界面活性剤) (CHLCH,O)、 H し 1 (一般式中n=2) 上記水と化合物(A)及びCB)及びグリセリンの混合
液に染料を完全熔解して後、残りの成分を添加混合攪拌
して黒色のスタンプインキを得た。
Example 2 Stamp ink C1, Direct B1ack51 20 (C1,
27720) ・Glycerin 56 ・Water 20 Sodium dodecylbenzenesulfonate 1 (surfactant) (CHLCH,O), H 1 (n=2 in the general formula) Mixture of the above water, compounds (A) and CB), and glycerin After the dye was completely dissolved in the liquid, the remaining components were added, mixed and stirred to obtain a black stamp ink.

実施例3筆記具用インキ C1,Ac1d Red87 10 (C1,45380) 水 6゜ エチレングリコール 28 安息香酸ナトリウム(防腐剤) I CH,CH。Example 3 Ink for writing instruments C1, Ac1d Red87 10 (C1,45380) Water 6゜ Ethylene glycol 28 Sodium benzoate (preservative) I CH, CH.

(一般式中a=b=2、c=1) (C1ちCH2O)、H 7 (一般式中n=2) 上記各成分を完全溶解して赤インキを得た。(In the general formula, a=b=2, c=1) (C1CH2O), H 7 (n=2 in the general formula) The above components were completely dissolved to obtain red ink.

実施例4筆記具用インキ C1,Ba5ic B1ue9 15 (C1,52015) 水 50 エチレングリコール 22 ジエチレングリコール 11 安息香酸ナトリウム(防腐剤) I CH□CH3 (一般式中a=b=l、c=2) CH,CH,OH ♂ (一般式中n=1) 上記各成分を完全熔解して青インキを得た。Example 4 Ink for writing instruments C1, Ba5ic B1ue9 15 (C1,52015) Water 50 Ethylene glycol 22 Diethylene glycol 11 Sodium benzoate (preservative) I CH□CH3 (In the general formula, a=b=l, c=2) CH, CH, OH ♂ (n=1 in the general formula) A blue ink was obtained by completely melting each of the above components.

上記実施例1.3.4のインキを市販のサインペンと同
様の筆記具に充填し室温でキャップを取り外して3週間
放置してもペン先に染料が析出しなく、筆記してもカス
レ等が生じなかった。又発色性も全く変化がなく初期筆
記線と同様の色調であった。
Even after filling a writing instrument similar to a commercially available felt-tip pen with the ink of Example 1.3.4 and leaving it at room temperature for 3 weeks with the cap removed, the dye did not precipitate on the pen tip, and writing did not cause smudging. There wasn't. Furthermore, there was no change in color development, and the color tone was the same as that of the initial writing line.

上記実施例2、のインキを市販のスタンプ台に充填しゴ
ム印判にて捺印すると鮮明な捺印ができ又、耐水性も良
好であった。
When a commercially available stamp pad was filled with the ink of Example 2 and stamped with a rubber stamp, a clear stamp was obtained and the water resistance was also good.

以上that's all

Claims (1)

【特許請求の範囲】 水溶性染料の水溶液に下記一般式よりなる(A)又は(
B)を配合したことを特徴とするインキC11,CH。 (1≦a≦5) (l≦b≦5) (1≦C≦5)(C
H,CI、O)、H 1 (1≦n≦5)
[Scope of Claims] In an aqueous solution of a water-soluble dye, (A) or (
Ink C11, CH characterized by containing B). (1≦a≦5) (l≦b≦5) (1≦C≦5) (C
H, CI, O), H 1 (1≦n≦5)
JP58232926A 1983-12-09 1983-12-09 Ink Granted JPS60124670A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58232926A JPS60124670A (en) 1983-12-09 1983-12-09 Ink

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58232926A JPS60124670A (en) 1983-12-09 1983-12-09 Ink

Publications (2)

Publication Number Publication Date
JPS60124670A true JPS60124670A (en) 1985-07-03
JPH0142308B2 JPH0142308B2 (en) 1989-09-12

Family

ID=16947001

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58232926A Granted JPS60124670A (en) 1983-12-09 1983-12-09 Ink

Country Status (1)

Country Link
JP (1) JPS60124670A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5389134A (en) * 1994-07-18 1995-02-14 Xerox Corporation Ink compositions for ink jet printing
US7229488B2 (en) 2005-09-06 2007-06-12 Samsung Electronics Co., Ltd. Ink composition, ink cartridge including the same, and inkjet image forming apparatus including the ink cartridge

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5389134A (en) * 1994-07-18 1995-02-14 Xerox Corporation Ink compositions for ink jet printing
US7229488B2 (en) 2005-09-06 2007-06-12 Samsung Electronics Co., Ltd. Ink composition, ink cartridge including the same, and inkjet image forming apparatus including the ink cartridge
KR100750129B1 (en) 2005-09-06 2007-08-21 삼성전자주식회사 Ink composition, ink cartridge and ink jet recording apparatus including the same

Also Published As

Publication number Publication date
JPH0142308B2 (en) 1989-09-12

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