JPS6377982A - Ink composition for marking pen - Google Patents
Ink composition for marking penInfo
- Publication number
- JPS6377982A JPS6377982A JP61221287A JP22128786A JPS6377982A JP S6377982 A JPS6377982 A JP S6377982A JP 61221287 A JP61221287 A JP 61221287A JP 22128786 A JP22128786 A JP 22128786A JP S6377982 A JPS6377982 A JP S6377982A
- Authority
- JP
- Japan
- Prior art keywords
- hydrocarbon chain
- organic compound
- ink composition
- amount
- ethyl alcohol
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002904 solvent Substances 0.000 claims abstract description 11
- 235000019441 ethanol Nutrition 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000002894 organic compounds Chemical class 0.000 abstract description 11
- 150000002430 hydrocarbons Chemical group 0.000 abstract description 8
- 238000001035 drying Methods 0.000 abstract description 6
- 239000011347 resin Substances 0.000 abstract description 3
- 229920005989 resin Polymers 0.000 abstract description 3
- 239000004094 surface-active agent Substances 0.000 abstract description 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 125000001165 hydrophobic group Chemical group 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はノンドライ性を向上させたマーキングペン用イ
ンキ組成物に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an ink composition for marking pens with improved non-drying properties.
(従来の技術)
従来、マーキングペン用インキ組成物の溶剤としてキシ
レンやセロソルブ等が用いられていたが毒性に問題があ
った。そこで毒性の低いエチルアルコールを溶剤として
用いることが望まれるが、エチルアルコールは揮発性が
高くドライアップ時間が短かい°の、でキャツlプオフ
状態ではすぐに筆記不能に陥る欠点があった。一般にノ
ンドライ性を向上させるには、中高佛点溶剤や遅乾性溶
剤が添加されるが、これらの溶剤を添加すると毒性の点
でエチルアルコールの低毒性のメリットを半減させる欠
点があシ、又、これらの溶剤は高粘度であるので添加量
が多くなるとインキの流動性が損われる問題がある。(Prior Art) Conventionally, xylene, cellosolve, etc. have been used as solvents for ink compositions for marking pens, but they have had problems with toxicity. Therefore, it is desirable to use ethyl alcohol, which has low toxicity, as a solvent, but ethyl alcohol has the disadvantage that it is highly volatile and requires a short dry-up time, so that it becomes impossible to write on it immediately in the cap-off state. Generally, to improve non-drying properties, medium-to-high temperature solvents and slow-drying solvents are added, but adding these solvents has the disadvantage of halving the low toxicity advantage of ethyl alcohol. Since these solvents have high viscosity, there is a problem that the fluidity of the ink is impaired when the amount added is large.
(発明が解決しようとする問題点)
そこで本発明は、毒性に問題なく、又、粘度も流動性を
損なうほど高くならず、ノンドライ性が向上するマーキ
ングペン用インキ組成物の提供を目的とするものである
。(Problems to be Solved by the Invention) Therefore, an object of the present invention is to provide an ink composition for a marking pen that has no toxicity problems, does not have a viscosity so high as to impair fluidity, and has improved non-drying properties. It is something.
(問題点を解決するための手段)
上記目的を達成するために案出された本願のマーキング
ペン用インキ組成物は、溶剤としてエチルアルコールを
用い、又、以下の分子式%式%)
(Rは炭素数が16〜22の炭化水素鎖でnは0〜5の
整数)
(2) R−100H
(Rは炭素数が16〜18の炭化水素鎖)・(3)R−
OH
(Rは炭素数が16〜22の炭化水素鎖)で示されるい
ずれかの有機化合物を(1)の場合は0.2〜4.0i
量嗟、(2)の場合は0.2〜2.0順11′(3)の
場合は0.2〜,2.0重量%の範囲で添加せしめたと
とを特徴とするものである。尚、上記有機化合物の内で
(3)の炭化水素鎖の炭素数は16〜18の範囲がよシ
好ましい。又、これら有機化合物の添加量も、(1)の
場合は0.8〜3.0重量%、(2)の場合は0.6〜
1.5重量%、(3)の場合は0.6〜1.5重量−の
範囲がより好ましい、添加量が少な過ぎると効果が現れ
ず、又、逆に多すぎると溶解せず仮に溶解しても再析出
する恐れがあるからである。インキ組成物には勿論染料
や他の所要なレジンが所要量含有される。(Means for Solving the Problems) The ink composition for marking pens of the present application devised to achieve the above object uses ethyl alcohol as a solvent and has the following molecular formula (% formula %) (R is Hydrocarbon chain having 16 to 22 carbon atoms, n is an integer of 0 to 5) (2) R-100H (R is a hydrocarbon chain having 16 to 18 carbon atoms) (3) R-
In the case of (1), 0.2 to 4.0i of any organic compound represented by OH (R is a hydrocarbon chain having 16 to 22 carbon atoms)
In case of (2), it is added in an amount of 0.2 to 2.0% by weight, and in case of (3), it is added in an amount of 0.2 to 2.0% by weight. In addition, among the above organic compounds, the number of carbon atoms in the hydrocarbon chain of (3) is preferably in the range of 16 to 18. Also, the amount of these organic compounds added is 0.8 to 3.0% by weight in the case of (1), and 0.6 to 3.0% in the case of (2).
1.5% by weight, and in the case of (3), the range of 0.6 to 1.5% by weight is more preferable. If the amount added is too small, the effect will not appear, and conversely, if it is too large, it will not dissolve and will not dissolve. This is because there is a risk of re-precipitation. The ink composition naturally contains the required amount of dye and other necessary resins.
(作用)
本願は上記(1)、(2)、(3)のいずれかの有機化
合物を界面活性剤として添加するととくよシ気液形成し
、溶剤6フンドライ性の向上を図るものである。斯る有
機化合物は疎水基である炭化水素鎖(R)と、親水基で
ある−(C!Ha O)n H1−(X)OH−OH等
からなる。これら有機化合物が気液界面に単分子膜を形
成するか否かは、親水基の水に対する親和力の程度と疎
水基間に働く凝集力の大キさとのバランスによって定ま
る。即ち親水基の親水性が弱いと単分子膜の形成は不可
能であシ逆に強すぎても水に溶解して単分子膜は得られ
ない。又、疎水基の凝集力は疎水基の長さが長いほど大
きく、あまシ短いと親水基の効果がこれに打ちがち分子
は水に溶解してしまい単分子膜は得られない。本願がと
こに提示した界■活性剤として添加する有機化合物の種
類とその添加量は、本発明者が鋭意研究及び実験を行な
った結果得られたもので、親水基の親水性の2イ性を向
上させることが可能となるものである。(Function) According to the present invention, when the organic compound of any one of the above (1), (2), and (3) is added as a surfactant, gas and liquid are formed to improve the solvent 6-fund drying properties. Such an organic compound consists of a hydrocarbon chain (R) which is a hydrophobic group, and -(C!HaO)nH1-(X)OH-OH, which is a hydrophilic group. Whether or not these organic compounds form a monomolecular film at the gas-liquid interface is determined by the balance between the degree of affinity for water of the hydrophilic groups and the magnitude of the cohesive force acting between the hydrophobic groups. That is, if the hydrophilicity of the hydrophilic group is weak, it is impossible to form a monomolecular film, whereas if it is too strong, it dissolves in water and a monomolecular film cannot be obtained. Furthermore, the cohesive force of a hydrophobic group increases as the length of the hydrophobic group increases; if the length of the hydrophobic group is too short, the effect of the hydrophilic group tends to overcome this, and the molecules dissolve in water, making it impossible to obtain a monomolecular film. The types and amounts of organic compounds to be added as surfactants presented herein in this application were obtained as a result of intensive research and experiments by the inventors, and are This makes it possible to improve the
(実施例)
以下に本発明の第1実施例〜第4実施例と比較例の組成
と、併せてドライアップまでの時間を計測した実験結果
を表によって示す。尚、表中の染料及び他の添加レジン
は適宜なものを使用し、溶剤は工業用変性エチルアルプ
ールを使用した。(Example) Below, the compositions of the first to fourth examples of the present invention and comparative examples, as well as the experimental results of measuring the time until dry-up, are shown in a table. In addition, appropriate dyes and other additive resins were used in the table, and industrial modified ethyl alpour was used as a solvent.
第1実施例の組成
第2実施例の組成
第3実施例の組成
第4実施例の組成
比較例
実験結果
(発明の効果)
本発明のマーキングペン用インΦ組成物は上述した如く
、毒性の心配がなく、又、流動性を阻害するほどに粘度
が高くなることもなく、ノンドライ性を極めて向上させ
る効果がある。Composition of First Example Composition of Second Example Composition of Third Example Composition of Fourth Example Comparative Example Experimental Results (Effects of the Invention) As described above, the ink composition for marking pens of the present invention is free from toxicity. There is no need to worry, and the viscosity does not become so high that it impedes fluidity, and it has the effect of extremely improving non-dry properties.
Claims (1)
整数) (2)R−COOH (Rは炭素数が16〜18の炭化水素鎖) (3)R−OH (Rは炭素数が16〜22の炭化水素鎖) で示されるいずれかの有機化合物を(1)の場合は0.
2〜4.0重量%、(2)の場合は0.2〜2.0重量
%、(3)の場合は0.2〜2.0重量%の範囲で添加
せしめたことを特徴とするマーキングペン用インキ組成
物。[Claims] Ethyl alcohol is used as a solvent, and the following molecular formula (1) R-O-(C_2H_4O)_nH (R is a hydrocarbon chain having 16 to 22 carbon atoms and n is an integer of 0 to 5) ) (2) R-COOH (R is a hydrocarbon chain having 16 to 18 carbon atoms) (3) R-OH (R is a hydrocarbon chain having 16 to 22 carbon atoms) In case of (1), 0.
It is characterized in that it is added in a range of 2 to 4.0% by weight, 0.2 to 2.0% by weight in case of (2), and 0.2 to 2.0% by weight in case of (3). Ink composition for marking pens.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61221287A JPS6377982A (en) | 1986-09-19 | 1986-09-19 | Ink composition for marking pen |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61221287A JPS6377982A (en) | 1986-09-19 | 1986-09-19 | Ink composition for marking pen |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6377982A true JPS6377982A (en) | 1988-04-08 |
JPH0571065B2 JPH0571065B2 (en) | 1993-10-06 |
Family
ID=16764416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61221287A Granted JPS6377982A (en) | 1986-09-19 | 1986-09-19 | Ink composition for marking pen |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6377982A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994000522A1 (en) * | 1992-06-19 | 1994-01-06 | Mitsubishi Pencil Kabushiki Kaisha | Ethanolic ink for marking pen |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4929A (en) * | 1972-04-13 | 1974-01-05 | ||
JPS5554370A (en) * | 1978-10-18 | 1980-04-21 | Pilot Ink Co Ltd | Ink for ball point pen |
JPS55137175A (en) * | 1979-04-12 | 1980-10-25 | Daiwa Maakanto Kogyo Kk | Ink composition for skin marking |
JPS5736173A (en) * | 1980-08-15 | 1982-02-26 | Mitsubishi Pencil Co Ltd | Ink for ball-point pen |
JPS5974174A (en) * | 1982-10-20 | 1984-04-26 | Pilot Ink Co Ltd | Metallic color ink for marking pen |
JPS6086183A (en) * | 1983-10-17 | 1985-05-15 | Pentel Kk | Marking ink composition |
-
1986
- 1986-09-19 JP JP61221287A patent/JPS6377982A/en active Granted
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4929A (en) * | 1972-04-13 | 1974-01-05 | ||
JPS5554370A (en) * | 1978-10-18 | 1980-04-21 | Pilot Ink Co Ltd | Ink for ball point pen |
JPS55137175A (en) * | 1979-04-12 | 1980-10-25 | Daiwa Maakanto Kogyo Kk | Ink composition for skin marking |
JPS5736173A (en) * | 1980-08-15 | 1982-02-26 | Mitsubishi Pencil Co Ltd | Ink for ball-point pen |
JPS5974174A (en) * | 1982-10-20 | 1984-04-26 | Pilot Ink Co Ltd | Metallic color ink for marking pen |
JPS6086183A (en) * | 1983-10-17 | 1985-05-15 | Pentel Kk | Marking ink composition |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994000522A1 (en) * | 1992-06-19 | 1994-01-06 | Mitsubishi Pencil Kabushiki Kaisha | Ethanolic ink for marking pen |
US5423907A (en) * | 1992-06-19 | 1995-06-13 | Mitsubishi Pencil Kabushiki Kaibha | Ethanol-based ink for marking pens |
Also Published As
Publication number | Publication date |
---|---|
JPH0571065B2 (en) | 1993-10-06 |
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