JPH11279475A - Oily ink for marking pen - Google Patents

Oily ink for marking pen

Info

Publication number
JPH11279475A
JPH11279475A JP10000498A JP10000498A JPH11279475A JP H11279475 A JPH11279475 A JP H11279475A JP 10000498 A JP10000498 A JP 10000498A JP 10000498 A JP10000498 A JP 10000498A JP H11279475 A JPH11279475 A JP H11279475A
Authority
JP
Japan
Prior art keywords
oil
weight
fatty acid
ink
marking pen
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
JP10000498A
Other languages
Japanese (ja)
Other versions
JP3909951B2 (en
Inventor
Kikutoshi Ueda
喜久利 上田
Masahiro Matsuoka
正弘 松岡
Takeshi Nakano
健 中野
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.)
Shachihata Inc
Original Assignee
Shachihata Inc
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 Shachihata Inc filed Critical Shachihata Inc
Priority to JP10000498A priority Critical patent/JP3909951B2/en
Publication of JPH11279475A publication Critical patent/JPH11279475A/en
Application granted granted Critical
Publication of JP3909951B2 publication Critical patent/JP3909951B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain an oily ink having such mutually contradictory performances as dry-up resistance and short setting time. SOLUTION: This oily ink for marking pens essentially comprises a dye, an organic solvent, a resin soluble to the above organic solvent, and a saturated fatty acid ester which is made from a higher fatty acid selected from tetradecanoic acid, pentadecanoic acid and hexadecanoic acid and a higher aliphatic alcohol selected from tetradecanol, pentadecanol, hexadecanol, heptadecanol and octadecanol.

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、筆記対象物が吸収
性・非吸収性にかかわらず筆記できるいわゆる速乾性油
性マーキングペンに用いられる油性インキに関するもの
である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an oil-based ink used for a so-called quick-drying oil-based marking pen which allows a writing object to be written irrespective of absorbency or non-absorptivity.

【0002】[0002]

【従来の技術】速乾性油性マーキングペンは、紙だけで
なく、ガラス・陶磁器・布などにも筆記でき、筆記後は
筆記線がすみやかに乾燥する特徴があるが、その一方、
キャップを外したまま放置しておくと、ペン先が乾燥し
て樹脂等が硬化し、筆記不可能となる欠点があった。い
わゆるドライアップである。この欠点を解決すべく各種
ドライアップ防止剤を含有させた油性インキとして、特
開昭51−120826、特公昭52−44244、特
開昭57−28177、特開昭61−34080、特開
昭61−261380、特開昭62−135578等が
開示されている。しかし、ドライアップを有効に防止で
きる程度までにするには、前記ドライアップ防止剤を多
量に配合させなければなず、そうすると今度は油性イン
キの最大の特徴である筆記線の乾燥時間(以下、「セッ
ト時間」という。)が遅くなるという新たな欠点が生じ
ていた。
2. Description of the Related Art A quick-drying oil-based marking pen can be written not only on paper but also on glass, ceramics, cloth, etc., and after writing, the writing line dries quickly.
If the cap is left with the cap removed, the pen tip dries and the resin or the like hardens, and there is a drawback that writing becomes impossible. This is what is called dry-up. In order to solve this drawback, oil-based inks containing various dry-up inhibitors are disclosed in JP-A-51-120826, JP-B-52-44244, JP-A-57-28177, JP-A-61-34080 and JP-A-61-34080. -261380 and JP-A-62-135578. However, in order to effectively prevent dry-up, the dry-up inhibitor must be incorporated in a large amount, and then the drying time of the writing line, which is the most characteristic of oil-based ink (hereinafter, referred to as There is a new disadvantage that the "set time" is delayed.

【0003】[0003]

【発明が解決しようとする課題】そこで、本出願人は研
究の結果、耐ドライアップ性と短セット時間といった相
反する性能を具備した油性インキを見出すことに成功し
た。
Accordingly, as a result of research, the present applicant has succeeded in finding an oil-based ink having contradictory properties such as dry-up resistance and short set time.

【0004】[0004]

【課題を解決するための手段】染料、有機溶剤、前記有
機溶剤に可溶な樹脂、飽和脂肪酸エステルを少なくとも
含有するマーキングペン用油性インキであって、前記飽
和脂肪酸エステルがテトラデカン酸又はペンタデカン酸
又はヘキサデカン酸から選ばれる高級脂肪酸とテトラデ
カノール又はペンタデカノール又はヘキサデカノール又
はヘプタデカノール又はオクタデカノールから選ばれる
高級脂肪族アルコールとの飽和脂肪酸エステルであるイ
ンキによって、前記課題を解決できる。また、前記染料
が、造塩タイプ油溶性染料であり、前記有機溶剤が、メ
タノール、エタノール、プロパノール、ブタノールから
選ばれる単独又は2以上を混合してなる低級脂肪族アル
コール、又は、前記低級脂肪族アルコールと乳酸エステ
ルの混合溶剤であり、前記樹脂が、ケトンホルムアルデ
ヒド樹脂、又は、アルキルフェノール樹脂、又は、ロジ
ン変性樹脂であるインキは更に好ましい。また、前記飽
和脂肪酸エステルが、インキ全量に対して0.01重量
%〜1.00重量%、特に0.55重量%〜0.95重
量%であるインキは更に好ましい。
An oil-based ink for a marking pen containing at least a dye, an organic solvent, a resin soluble in the organic solvent, and a saturated fatty acid ester, wherein the saturated fatty acid ester is tetradecanoic acid or pentadecanoic acid or This problem can be solved by an ink that is a saturated fatty acid ester of a higher fatty acid selected from hexadecanoic acid and a higher fatty alcohol selected from tetradecanol, pentadecanol, hexadecanol, heptadecanol, or octadecanol. In addition, the dye is a salt-forming type oil-soluble dye, and the organic solvent is methanol, ethanol, propanol, a lower aliphatic alcohol alone or a mixture of two or more selected from butanol, or the lower aliphatic alcohol. An ink which is a mixed solvent of an alcohol and a lactic acid ester, and wherein the resin is a ketone formaldehyde resin, an alkylphenol resin, or a rosin-modified resin, is more preferable. Further, an ink in which the saturated fatty acid ester is 0.01% by weight to 1.00% by weight, particularly 0.55% by weight to 0.95% by weight, based on the total amount of the ink is more preferred.

【0005】以下、本発明を詳細に説明する。本発明で
は着色剤として油溶性染料を用い、油性マーキングペン
用染料として一般に市販されているモノアゾ、ジスア
ゾ、金属錯塩型モノアゾ、アントラキノン、フタロシア
ニン、トリアリルメタン等の油溶性染料を用いることが
できるが、中でも造塩タイプ油溶性染料が最も好ましい
結果を示す。造塩タイプ油溶性染料は、酸性染料・直接
染料・塩基性染料等の親水基を疎水基に置換した染料で
あって、本発明では、酸性染料の親水基をカチオン活性
剤・樹脂塩基・アミン・塩基性染料等の疎水基で置換し
たもの、直接染料の親水基をカチオン活性剤・樹脂塩基
・アミン・塩基性染料等の疎水基で置換したもの、塩基
性染料の親水基をアニオン活性剤・樹脂酸・酸性染料・
直接染料等の疎水基で置換したものを使用できる。
Hereinafter, the present invention will be described in detail. In the present invention, an oil-soluble dye is used as a coloring agent, and an oil-soluble dye such as monoazo, disazo, metal complex salt type monoazo, anthraquinone, phthalocyanine, and triallylmethane, which are generally commercially available as an oil-based marking pen dye, can be used. Among them, salt-forming type oil-soluble dyes show the most preferable results. Salt-forming type oil-soluble dyes are dyes in which hydrophilic groups such as acid dyes, direct dyes, and basic dyes are substituted with hydrophobic groups.In the present invention, the hydrophilic groups of the acid dyes are replaced with cationic activators, resin bases, amines.・ Substituted with a hydrophobic group such as a basic dye, etc., the hydrophilic group of the direct dye is replaced with a cationic activator ・ Resin base ・ Amine ・ Substituted with a hydrophobic group such as a basic dye, etc., and the hydrophilic group of a basic dye is an anionic activator・ Resin acid ・ acid dye ・
Those directly substituted with a hydrophobic group such as a dye can be used.

【0006】有機溶剤は、低級脂肪族アルコールが必須
であり、メタノール、エタノール、プロパノール、ブタ
ノールから選択する。プロパノール、ブタノールは、そ
れぞれ異性体が存在するが、ノルマル、イソ、ターシャ
ル等すべての構造のものが使用可能である。低級脂肪族
アルコールは、単独で使用しても良いし、2以上を混合
して使用しも良い。また、これら低級脂肪族アルコール
と乳酸エステルを混合して使用して良好な結果が得られ
る。乳酸エステルとしては、乳酸メチル、乳酸エチル、
乳酸プロピル、乳酸ブチルから選択する。乳酸プロピ
ル、乳酸ブチルは、それぞれ異性体が存在するが、ノル
マル、イソ、ターシャル等すべての構造のものが使用可
能である。
As the organic solvent, a lower aliphatic alcohol is essential, and is selected from methanol, ethanol, propanol and butanol. Propanol and butanol have respective isomers, but those having any structure such as normal, iso, and tertal can be used. The lower aliphatic alcohols may be used alone or as a mixture of two or more. Good results can be obtained by using a mixture of these lower aliphatic alcohols and lactic acid esters. As lactate, methyl lactate, ethyl lactate,
Choose from propyl lactate and butyl lactate. Although propyl lactate and butyl lactate have respective isomers, those having any structure such as normal, iso, and tertal can be used.

【0007】樹脂は、油溶性樹脂を用い、ロジン樹脂、
エステル樹脂、セルロース樹脂、フェノール樹脂等を用
いることができるが、特に、ケトンホルムアルデヒド樹
脂、アルキルフェノール樹脂が好ましく用いられる。
[0007] The resin is an oil-soluble resin, rosin resin,
Ester resins, cellulose resins, phenol resins, and the like can be used, but ketone formaldehyde resins and alkylphenol resins are particularly preferably used.

【0008】飽和脂肪酸エステルは、テトラデカン酸、
ペンタデカン酸、ヘキサデカン酸から選ばれる高級脂肪
酸と、テトラデカノール、ペンタデカノール、ヘキサデ
カノール、ヘプタデカノール、オクタデカノールから選
ばれる高級脂肪族アルコールとの飽和脂肪酸エステルを
用いる。前記高級脂肪酸と前記高級脂肪族アルコール
は、それぞれが多数の異性体を有しているが、エステル
化した飽和脂肪酸エステルの融点が20℃以下とならな
い組み合せであれば、直鎖、分枝鎖を問わず、いずれの
ものも使用できる。本発明では特に、テトラデカン酸テ
トラデシル、ヘキサデカン酸テトラデシル、テトラデカ
ン酸ヘキサデシル、ヘキサデカン酸ヘキサデシル、テト
ラデカン酸オクタデシル、ヘキサデカン酸オクタデシル
が好ましく用いられ、直鎖のものが最もよい結果を得
る。前記飽和脂肪酸エステルは単独又は2以上を混合し
て使用することができる。配合量は、インキ全量に対し
て0.01重量%〜1.00重量%の範囲で本願の効果
を発揮するが、0.55重量%〜0.95重量%の範囲
が特に好ましい結果を示す。
[0008] Saturated fatty acid esters include tetradecanoic acid,
A saturated fatty acid ester of a higher fatty acid selected from pentadecanoic acid and hexadecanoic acid and a higher fatty alcohol selected from tetradecanol, pentadecanol, hexadecanol, heptadecanol and octadecanol is used. The higher fatty acid and the higher aliphatic alcohol each have a large number of isomers. However, if the combination of the esterified saturated fatty acid esters does not have a melting point of 20 ° C. or lower, a straight chain or a branched chain may be used. Any one can be used. In the present invention, particularly, tetradecyl tetradecanoate, tetradecyl hexadecanoate, hexadecyl tetradecanoate, hexadecyl hexadecanoate, octadecyl tetradecanoate, and octadecyl hexadecanoate are preferably used. The saturated fatty acid esters can be used alone or in combination of two or more. The compounding amount exerts the effect of the present invention in the range of 0.01% by weight to 1.00% by weight based on the total amount of the ink, but the range of 0.55% by weight to 0.95% by weight shows particularly preferable results. .

【0009】また、本発明では、防腐剤、防かび剤、ア
ミン類等の染料溶解助剤、ベンジルアルコール等の浸透
剤など通常インキに用いられる添加剤を添加することが
できる。
In the present invention, additives usually used for inks such as preservatives, fungicides, dye dissolution aids such as amines, and penetrants such as benzyl alcohol can be added.

【0010】[0010]

【実施例】以下、本発明を実施例をもって説明する。 (実施例1) タートラジンとローダミン6Gの造塩染料 6.0重量% エタノール 66.0重量% 乳酸エチル 16.0重量% アルキルフェノール樹脂 11.4重量% テトラデカン酸テトラデシル 0.3重量% ヘキサデカン酸ヘキサデシル 0.3重量% 以上の物質を混合し、赤色インキを得た。 (比較例1)実施例1からテトラデカン酸テトラデシル
とヘキサデカン酸ヘキサデシルを除いて赤色インキを作
成した。 (実施例2) ビクトリアピュアブルーと 酸性フタロシアニンブルーの造塩染料 6.0重量% エタノール 61.0重量% n−プロパノール 18.0重量% ケトンホルムアルデヒド樹脂 14.2重量% ヘキサデカン酸テトラデシル 0.5重量% テトラデカン酸オクタデシル 0.3重量% 以上の物質を混合し、青色インキを得た。(比較例2)
実施例2からヘキサデカン酸テトラデシルとテトラデカ
ン酸オクタデシルを除いて青色インキを作成した。 (実施例3) タートラジンとローダミン6Gの造塩染料 6.0重量% n−プロパノール 73.0重量% n−ブタノール 10.3重量% ケトンホルムアルデヒド樹脂 10.0重量% テトラデカン酸テトラデシル 0.2重量% テトラデカン酸ヘキサデシル 0.4重量% ヘキサデカン酸オクタデシル 0.1重量% 以上の物質を混合し、赤色インキを得た。(比較例3) 実施例3からテトラデカン酸テトラデシルとテトラデカ
ン酸ヘキサデシルとヘキサデカン酸オクタデシルを除い
て赤色インキを作成した。 (実施例4) タートラジンとローダミン6Gの造塩染料 6.0重量% エタノール 66.0重量% 乳酸エチル 16.0重量% アルキルフェノール樹脂 11.4重量% テトラデカン酸テトラデシル 0.1重量% ヘキサデカン酸ヘキサデシル 0.1重量% 以上の物質を混合し、赤色インキを得た。 (比較例4)実施例4からテトラデカン酸テトラデシル
とヘキサデカン酸ヘキサデシルを除いて赤色インキを作
成した。
The present invention will be described below with reference to examples. (Example 1) Salt-forming dye of tartrazine and rhodamine 6G 6.0% by weight Ethanol 66.0% by weight Ethyl lactate 16.0% by weight Alkylphenol resin 11.4% by weight Tetradecyl tetradecanoate 0.3% by weight Hexadecyl hexadecanoate 0 By mixing more than 0.3% by weight of a substance, a red ink was obtained. Comparative Example 1 A red ink was prepared from Example 1 except that tetradecyl tetradecanoate and hexadecyl hexadecanoate were removed. (Example 2) Salt forming dye of Victoria Pure Blue and acidic phthalocyanine blue 6.0% by weight Ethanol 61.0% by weight n-propanol 18.0% by weight Ketone formaldehyde resin 14.2% by weight Tetradecyl hexadecanoate 0.5% by weight % Octadecyl tetradecanoate 0.3% by weight or more was mixed to obtain a blue ink. (Comparative Example 2)
A blue ink was prepared by removing the tetradecyl hexadecanoate and octadecyl tetradecanoate from Example 2. (Example 3) Salt-forming dye of tartrazine and rhodamine 6G 6.0% by weight n-propanol 73.0% by weight n-butanol 10.3% by weight Ketone formaldehyde resin 10.0% by weight Tetradecyl tetradecanoate 0.2% by weight Hexadecyl tetradecanoate 0.4% by weight Hexadecyl hexadecanoate 0.1% by weight or more was mixed to obtain a red ink. Comparative Example 3 A red ink was prepared from Example 3 except that tetradecyl tetradecanoate, hexadecyl tetradecanoate, and octadecyl hexadecanoate were removed. (Example 4) Salt-forming dye of tartrazine and rhodamine 6G 6.0% by weight Ethanol 66.0% by weight Ethyl lactate 16.0% by weight Alkyl phenol resin 11.4% by weight Tetradecyl tetradecanoate 0.1% by weight Hexadecyl hexadecanoate 0 0.1% by weight or more of the substance was mixed to obtain a red ink. Comparative Example 4 A red ink was prepared by removing tetradecyl tetradecanoate and hexadecyl hexadecanoate from Example 4.

【0011】繊維ペン芯とインキ吸収体を備えた本体と
キャップとからなるマーキングペンに前記実施例及び比
較例のインキを充填し試験を行なった。温度20℃・湿
度65%の室内において、前記マーキングペンのキャッ
プを外した状態で8時間放置した後、紙面に筆記し、書
き出し直後の筆記性を調査した。 ○:鮮明な筆記線が得られた。 ×:かすれた筆記線しか得られなかった。 前記マーキングペンを用いてポリプロピレン製OHPフ
ィルムに筆記し、セット時間を調べた。以下、試験結果
を表にする。
A test was conducted by filling the marking pens comprising a main body having a fiber pen core, an ink absorber and a cap with the inks of the above Examples and Comparative Examples. After leaving the cap of the marking pen for 8 hours in a room at a temperature of 20 ° C. and a humidity of 65%, the marking pen was left untouched for 8 hours, and then written on paper to examine the writability immediately after writing. :: A clear writing line was obtained. X: Only a faint writing line was obtained. Writing was performed on an OHP film made of polypropylene using the marking pen, and the set time was examined. The test results are listed below.

【0012】[0012]

【表1】 [Table 1]

【0013】[0013]

【効果】特定の飽和脂肪酸エステルを配合したため、キ
ャップを外したまま放置しておいてもペン先にて弱い皮
膜を形成し、インキのドライアップを防止できる。再度
筆記する際は、皮膜が容易に壊れて筆記可能となる。ま
た、本発明はセット時間が影響されないので、すぐに乾
燥する筆記線を得られる。
[Effect] Since a specific saturated fatty acid ester is blended, a weak film is formed at the pen tip even if the cap is left unattended, so that dry-up of the ink can be prevented. When writing again, the film is easily broken and writing is possible. Further, since the present invention is not affected by the setting time, a writing line which dries quickly can be obtained.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 染料、有機溶剤、前記有機溶剤に可溶な
樹脂、飽和脂肪酸エステルを少なくとも含有するマーキ
ングペン用油性インキであって、前記飽和脂肪酸エステ
ルがテトラデカン酸又はペンタデカン酸又はヘキサデカ
ン酸から選ばれる高級脂肪酸とテトラデカノール又はペ
ンタデカノール又はヘキサデカノール又はヘプタデカノ
ール又はオクタデカノールから選ばれる高級脂肪族アル
コールとの飽和脂肪酸エステルであるマーキングペン用
油性インキ。
1. An oil-based ink for a marking pen containing at least a dye, an organic solvent, a resin soluble in the organic solvent, and a saturated fatty acid ester, wherein the saturated fatty acid ester is selected from tetradecanoic acid, pentadecanoic acid, and hexadecanoic acid. Oil for a marking pen, which is a saturated fatty acid ester of a higher fatty acid and a higher fatty alcohol selected from tetradecanol, pentadecanol, hexadecanol, heptadecanol or octadecanol.
【請求項2】 前記染料が、造塩タイプ油溶性染料であ
る請求項1のマーキングペン用油性インキ。
2. The oil-based ink for a marking pen according to claim 1, wherein the dye is a salt-forming type oil-soluble dye.
【請求項3】 前記有機溶剤が、メタノール、エタノー
ル、プロパノール、ブタノールから選ばれる単独又は2
以上を混合してなる低級脂肪族アルコール、又は、前記
低級脂肪族アルコールと乳酸エステルの混合溶剤である
請求項1のマーキングペン用油性インキ。
3. The method according to claim 1, wherein the organic solvent is selected from methanol, ethanol, propanol, and butanol.
The oil-based ink for a marking pen according to claim 1, which is a lower aliphatic alcohol obtained by mixing the above, or a mixed solvent of the lower aliphatic alcohol and a lactic acid ester.
【請求項4】 前記樹脂が、ケトンホルムアルデヒド樹
脂、又は、アルキルフェノール樹脂、又は、ロジン変性
樹脂である請求項1のマーキンペン用インキ。
4. The ink for a marker pens according to claim 1, wherein the resin is a ketone formaldehyde resin, an alkylphenol resin, or a rosin-modified resin.
【請求項5】 インキ全量に対して、前記飽和脂肪酸エ
ステルが0.01重量%〜1.00重量%である請求項
1のマーキングペン用油性インキ。
5. The oil-based ink for a marking pen according to claim 1, wherein the content of the saturated fatty acid ester is 0.01% by weight to 1.00% by weight based on the total amount of the ink.
【請求項6】 インキ全量に対して、前記飽和脂肪酸エ
ステルが0.55重量%〜0.95重量%である請求項
1のマーキングペン用油性インキ。
6. The oil-based ink for a marking pen according to claim 1, wherein the content of the saturated fatty acid ester is 0.55% by weight to 0.95% by weight based on the total amount of the ink.
JP10000498A 1998-03-27 1998-03-27 Oil-based ink for marking pens Expired - Fee Related JP3909951B2 (en)

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JP10000498A JP3909951B2 (en) 1998-03-27 1998-03-27 Oil-based ink for marking pens

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JPH11279475A true JPH11279475A (en) 1999-10-12
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004352918A (en) * 2003-05-30 2004-12-16 Pentel Corp Oily green ink

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004352918A (en) * 2003-05-30 2004-12-16 Pentel Corp Oily green ink

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