JPS5941369A - Ink composition with alcohol as chief solvent - Google Patents

Ink composition with alcohol as chief solvent

Info

Publication number
JPS5941369A
JPS5941369A JP15245182A JP15245182A JPS5941369A JP S5941369 A JPS5941369 A JP S5941369A JP 15245182 A JP15245182 A JP 15245182A JP 15245182 A JP15245182 A JP 15245182A JP S5941369 A JPS5941369 A JP S5941369A
Authority
JP
Japan
Prior art keywords
alcohol
solvent
pref
pyridine
ink
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP15245182A
Other languages
Japanese (ja)
Inventor
Hisanari Fujita
尚成 藤田
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.)
Sakura Color Products Corp
Original Assignee
Sakura Color Products Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sakura Color Products Corp filed Critical Sakura Color Products Corp
Priority to JP15245182A priority Critical patent/JPS5941369A/en
Publication of JPS5941369A publication Critical patent/JPS5941369A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To provide titled composition prevented from chalking, free from clogging and/or ink blur, thus improved in writing characteristics, comprising a dye or pigment, alcohol solvent, alcohol-soluble resin, and hydroxyalkyl pyridine derivative of specific formula. CONSTITUTION:The objective composition comprising (A) a dye or pigment, (B) pref. 50-75wt% of an alcohol solvent such as ethanol, ethylene glycol monoethyl ether, (C) pref. 7-13wt% of an alcohol-soluble resin such as phenolic or ketone resin, and (D) pref. 2-7wt% of a hydroxyalkyl pyridine derivative of formula (R is H, or 1-4C alkyl; n is 1-4) (e.g., propanol pyridine, 2-methyl-6- propanol pyridine). USE:For marking pen, ball point pen for low-viscosity ink, writing utensils for recorders, and stamping.

Description

【発明の詳細な説明】 この発明はマーキングペン、低粘性インキ用ボールペン
、Yl[1録計川自E記共、al %ず代筆ii[!具
、尋の華tkl貝に用いるインキあるいはスタンプ用イ
ンキとして適性あるインキ組成物1こ関する。
[Detailed Description of the Invention] This invention is a marking pen, a ballpoint pen for low viscosity ink, Yl[1. The present invention relates to an ink composition suitable as an ink for use in gu, Hironohana TKL shells, or as an ink for stamps.

これらの・fンヰには炭化水素系、ケトン系、あるいは
エステル系溶剤を主溶剤とする油性インキ、氷、多価ア
ルコールを主成分とする水性インキの2拙に大別され前
者は速乾性であるが溶剤の臭気と毒性の問題があり、後
者は臭気と11性はないが遅乾性であり、それぞれ問題
点があった。両者の欠点を解決するものとして、アルコ
ール系溶剤およヒ/またはエチレングリコールアルキル
エーテル系溶剤を主溶剤とするアルコール性インキが出
まわっている。しかしアルコール性インキにも次に記す
ような欠点がある。
These inks are roughly divided into two types: oil-based inks whose main solvents are hydrocarbon, ketone, or ester solvents, and water-based inks whose main components are ice and polyhydric alcohols.The former is quick-drying. However, there are problems with the odor and toxicity of the solvent, and the latter does not have an odor or 11 properties, but is slow drying, and each has its own problems. In order to solve both of these drawbacks, alcohol-based inks containing alcohol-based solvents and/or ethylene glycol alkyl ether-based solvents as main solvents are on the market. However, alcohol-based inks also have drawbacks as described below.

11)  吸湿性があるので、筆跡が吸n刊シ樹脂成5
]が析出して白亜化の現象を起す。
11) Because it is hygroscopic, the handwriting will absorb
] precipitates and causes the phenomenon of chalking.

(2)筆記へに使用した場合、ペン先内のインキが吸湿
し水不溶性の樹脂成分が析出して1ずまりしインキかず
れ1iti己不I!iIAとなる。
(2) When used for writing, the ink inside the nib absorbs moisture and water-insoluble resin components precipitate, causing the ink to smear and cause damage! Become iIA.

この発明はアルコール性インード#、n JJQ ’l
勿において上記の欠点を19・Y決したもの−C゛、色
素、アルコール系ra剤、アルコール可溶性IJ JJ
!7および−ノυ式(1)で表わすヒドロキシアルキル
ピリジン誘導体よりなるアルコールを主ta剤とするイ
ンキ組成物である。
This invention is an alcoholic Indian #,n JJQ'l
Of course, the above drawbacks have been resolved by 19.
! This is an ink composition whose main agent is an alcohol made of a hydroxyalkylpyridine derivative represented by the formula (1).

〔RはH又は炭素数1〜4のアルキル基、nは1〜4の
整数を示す。〕 コール可溶性染料が用いられ、例えば C,1,ソルベント・エロー 1. 3.  l 3.
 34゜C,1,ソルベント・オレンジ 24,25゜
C,1,ソルベント・レッド 34.49.67、69
゜C,1,ソルベントのバイオレット 10.16.2
4゜C,1,ソルベント・ブルー 2.16.30.3
3゜34、38.42゜ (、:、1.ソルベント・ブラック 14.17.19
゜20、28゜ C,I、ソルベント・グリーン 10,11゜C,1,
ソルベント・ブラウン 17.19.20゜31、35
.36゜ が例示できる。
[R represents H or an alkyl group having 1 to 4 carbon atoms, and n represents an integer of 1 to 4. ] Cole soluble dyes are used, such as C, 1, Solvent Yellow 1. 3. l 3.
34°C, 1, Solvent Orange 24, 25°C, 1, Solvent Red 34.49.67, 69
°C, 1, Solvent Violet 10.16.2
4°C, 1, Solvent Blue 2.16.30.3
3゜34, 38.42゜(,:,1.Solvent Black 14.17.19
゜20, 28゜C, I, Solvent Green 10, 11゜C, 1,
Solvent Brown 17.19.20゜31, 35
.. An example is 36°.

顔料を使用する場合は、通常の顔料はすべて使用できる
がアルコール可溶性樹脂で処理された、加工顔料が有利
でありフジASカラー(富士色素(株):商品名)、マ
イクロリスカラー(チバガイギー:商品名)、ダイミク
ロンカラー(大日精化(抹):商品名)が例示できる。
When using pigments, all normal pigments can be used, but processed pigments treated with alcohol-soluble resin are advantageous. (name) and Daimicron Color (Dainichiseika (trade name)) are examples.

この発明で用いられるアルコール系溶剤としては、メタ
ノール、エタノール、イソプロパツール、ブタノール等
の低級アルコール、エチレングリコールモノエチルエー
テル、エチレングリコールモノブチルエーテル等のエチ
レングリコールモノアルキルエーテル、が例示できる。
Examples of alcoholic solvents used in this invention include lower alcohols such as methanol, ethanol, isopropanol and butanol, and ethylene glycol monoalkyl ethers such as ethylene glycol monoethyl ether and ethylene glycol monobutyl ether.

アルコール系溶剤はインキ組成物全体の40〜8511
只%(以下+fi 4迂(・ちを%と上記ず)、好しく
は50〜75%が使用される。アルコール系溶剤のBI
MIIIぢ10%迄はベンジルアルコール、ジエチレン
グリコール七ツメチルエーテル等カルピトール類、エチ
レングリコールモノフェニルエーテル、n=AM酸ブチ
ル等のエステル系溶剤メチルイソブチルケトン等のケト
ン系溶剤を添加して溶解性を高め、あるいは蒸発速度を
調節することができる。
The alcohol solvent accounts for 40 to 8511 of the entire ink composition.
Only % (hereinafter referred to as %), preferably 50 to 75% is used. BI of alcohol solvent
Up to 10% MIII, add ester solvents such as benzyl alcohol, diethylene glycol 7-methyl ether, carpitols, ethylene glycol monophenyl ether, n=butyl AM acid, etc., and ketone solvents such as methyl isobutyl ketone to increase solubility. Alternatively, the evaporation rate can be adjusted.

この発明で使用するアルコール可溶性樹脂とはフェノー
ル樹脂、キシレン樹脂、ケトン樹脂、ロジンおよびその
誘導体、ポリビニルブチラール、シェラツク等の天然又
は合成樹脂が例示でき、中でもガラスプラスチックへの
定着をよくするにはフェノール樹脂、ケトン樹脂、ロジ
ンおよびその誘導体が好ましく用いられる。これらの樹
脂はインキ組成物全体の5・〜20 閂%<=妻和歇湊
彬寺肯と七藁分が、好しくは7〜13%が用いられる。
Examples of the alcohol-soluble resin used in this invention include natural or synthetic resins such as phenol resin, xylene resin, ketone resin, rosin and its derivatives, polyvinyl butyral, and shellac. Resins, ketone resins, rosins and their derivatives are preferably used. These resins are used in an amount of 5% to 20%, preferably 7% to 13%, of the entire ink composition.

樹脂が7%以下では被筆記面に定着しがたり、20%以
上では粘度が大きくなり過ぎる。
If the resin is less than 7%, it tends to stick to the writing surface, and if it is more than 20%, the viscosity becomes too high.

この発明で使用できるヒドロキシアルキルピリジン誘導
体としては、プロパツールピリジン、エタノールピリジ
ン、ビリジンカルビトーノペ2−メチル−6、プロパツ
ールピリジン、エタノールピユリン、あるいはプロパノ
−ルビ4リン等が例示でき、インキ組成物全量の()、
1〜10%が使用でき、好しくは2〜7%が使用できる
。0.1%より少いと白亜化防止の効果がなく、10%
より多いと乾燥がおそくなるし、多少臭気を伴う。その
他通常アルコール性インキに使用される活性剤、防腐剤
、香料等を添加することをさまたげない。
Examples of hydroxyalkylpyridine derivatives that can be used in the present invention include propatoolpyridine, ethanolpyridine, biridinecarbitonope-2-methyl-6, propatoolpyridine, ethanolpyridine, propanolpyridine, and propanolpyridine. total amount of things (),
1-10% can be used, preferably 2-7%. If it is less than 0.1%, there is no effect of preventing chalking, and 10%
If the amount is too large, drying will be delayed and there will be some odor. Other additives such as activators, preservatives, fragrances, etc. that are normally used in alcohol-based inks may be added.

これらの成分よりインキ組成物を調製するには、全成分
を秤bit、、デスパーに投入し、18〜50’Cにて
2〜4時間撹拌し均一に溶解した後、−過してインキ組
成物とする。
To prepare an ink composition from these components, all the components are put into a weighing machine and a despar, stirred at 18 to 50'C for 2 to 4 hours to dissolve uniformly, and then filtered to prepare the ink composition. Make it a thing.

次に実施例を13してこの発明を−1−明らかにする。Next, Example 13 will clarify the present invention.

実施例1 ヂポンファーストブラックRB    10%(商品名
、B A S F社製、C,1,アシッドブラック12
3のクローム自金属染ト()エタノール       
      75%2−プロパツールピリジン    
  5%ハイラックl l OHl 0部 (商品名、日立化成工業製ケトン樹脂)上記全成分をデ
スバーに投入し30’Cで3時間撹拌して黒色のインキ
を得た。
Example 1 Dipon Fast Black RB 10% (trade name, manufactured by BASF Co., Ltd., C,1, Acid Black 12
3. Chrome autometal dyeing ()ethanol
75% 2-propertool pyridine
0 parts of 5% Hylac 1 1 OH1 (trade name, ketone resin manufactured by Hitachi Chemical Co., Ltd.) All the above ingredients were put into a death bar and stirred at 30'C for 3 hours to obtain a black ink.

実施例2 オラゾールレッドaGL        5%(商品名
、チバガイギー社製) エチレングリコールモノメチルエーテル 肋%2(βヒ
ドロキシエチル)ピリジン   5%ニカノールI P
 100         10%(商品名、三菱ガス
化学工業製、フェノール変性キシレン樹脂) 実施例1に準じて赤色のインキを得た。
Example 2 Orazole Red aGL 5% (trade name, manufactured by Ciba Geigy) Ethylene glycol monomethyl ether 5% (β-hydroxyethyl)pyridine 5% Nicanol IP
100 10% (trade name, manufactured by Mitsubishi Gas Chemical Industries, Ltd., phenol-modified xylene resin) A red ink was obtained according to Example 1.

実施例3 スピリオンブルーCRM         5%(商品
名、深土ケ谷比学工栗製) エタノール             80%2−メチ
ル−6−プロパツールピリジン 5%フマルードNo、
 31          10%(商品名、荒用化学
工業製、ロジン変性マレイン酸樹脂) 実施例1にl−じてvt色のインキを得た。
Example 3 Spirion Blue CRM 5% (trade name, manufactured by Fukatogayahigakuri) Ethanol 80% 2-methyl-6-propatolpyridine 5% Fumarude No.
31 10% (trade name, manufactured by Arayo Kagaku Kogyo Co., Ltd., rosin-modified maleic acid resin) A VT color ink was obtained in accordance with Example 1.

実施例4 フジASブルー            8%(フジ色
素(株)製、加工顔料、顔料針はC01,74160) エタノール              80%3−プ
ロパツールピリジン       5%ヒタノール11
33          7%([1立化成、アルキル
フェノール樹脂)実施例1に準じて(たゾし7戸;昌工
冊を1途く)青色のインキを得た。)
Example 4 Fuji AS Blue 8% (manufactured by Fuji Shiroki Co., Ltd., processed pigment, pigment needle is C01,74160) Ethanol 80% 3-propertool pyridine 5% Hytanol 11
33 7% ([1 Ritsu Kasei, alkylphenol resin) According to Example 1 (Tazoshi 7 doors; Sho Koshu 1 cut) Blue ink was obtained. )

Claims (1)

【特許請求の範囲】 色素、アルコール系溶剤、アルコール可溶性樹脂および
一般式(1)で表わすヒドロキシアルキルピリジン誘導
体よりなるアルコールを主溶剤とするインキ組成物。 〔RはH又は炭素数1〜4のアルキル基、nは1〜4の
格数を示す〕
[Scope of Claims] An ink composition whose main solvent is an alcohol consisting of a pigment, an alcoholic solvent, an alcohol-soluble resin, and a hydroxyalkylpyridine derivative represented by the general formula (1). [R represents H or an alkyl group having 1 to 4 carbon atoms, and n represents a case number of 1 to 4]
JP15245182A 1982-08-31 1982-08-31 Ink composition with alcohol as chief solvent Pending JPS5941369A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15245182A JPS5941369A (en) 1982-08-31 1982-08-31 Ink composition with alcohol as chief solvent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15245182A JPS5941369A (en) 1982-08-31 1982-08-31 Ink composition with alcohol as chief solvent

Publications (1)

Publication Number Publication Date
JPS5941369A true JPS5941369A (en) 1984-03-07

Family

ID=15540803

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15245182A Pending JPS5941369A (en) 1982-08-31 1982-08-31 Ink composition with alcohol as chief solvent

Country Status (1)

Country Link
JP (1) JPS5941369A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4713083A (en) * 1984-07-06 1987-12-15 Toyo Soda Manufacturing Co., Ltd. Alcoholic solution of sulphonic acid-containing copolymer dyed with basic dye
JPS6322875A (en) * 1986-07-15 1988-01-30 Pentel Kk Oil based ink composition
JPS63113091A (en) * 1986-10-31 1988-05-18 Pentel Kk Oil-based ink
JPS63120780A (en) * 1986-11-10 1988-05-25 Tatsuro Takeuchi Marker ink for electrophotographic toner image
JPS63317572A (en) * 1987-06-19 1988-12-26 Tosoh Corp Writing black ink composition
JPH01120242A (en) * 1987-11-02 1989-05-12 Kowa Kogyo:Kk Corn cup maker
JPH02215870A (en) * 1989-02-16 1990-08-28 Koyo Kasei Kk Method for preventing blurring of marking ink using felt core
FR2678941A1 (en) * 1991-07-12 1993-01-15 Mitsubishi Pencil Co ALCOHOL - BASED INK COMPOSITION FOR MARKER.

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4713083A (en) * 1984-07-06 1987-12-15 Toyo Soda Manufacturing Co., Ltd. Alcoholic solution of sulphonic acid-containing copolymer dyed with basic dye
JPS6322875A (en) * 1986-07-15 1988-01-30 Pentel Kk Oil based ink composition
JPS63113091A (en) * 1986-10-31 1988-05-18 Pentel Kk Oil-based ink
JPS63120780A (en) * 1986-11-10 1988-05-25 Tatsuro Takeuchi Marker ink for electrophotographic toner image
JPS63317572A (en) * 1987-06-19 1988-12-26 Tosoh Corp Writing black ink composition
JPH01120242A (en) * 1987-11-02 1989-05-12 Kowa Kogyo:Kk Corn cup maker
JPH02215870A (en) * 1989-02-16 1990-08-28 Koyo Kasei Kk Method for preventing blurring of marking ink using felt core
FR2678941A1 (en) * 1991-07-12 1993-01-15 Mitsubishi Pencil Co ALCOHOL - BASED INK COMPOSITION FOR MARKER.
US5279653A (en) * 1991-07-12 1994-01-18 Mitsubishi Pencil Kabushiki Kaisha Alcoholic marking pen ink composition

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