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JPH0768484B2 - Marking ink composition - Google Patents
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JPH0768484B2 - Marking ink composition - Google Patents

Marking ink composition

Info

Publication number
JPH0768484B2
JPH0768484B2 JP61204563A JP20456386A JPH0768484B2 JP H0768484 B2 JPH0768484 B2 JP H0768484B2 JP 61204563 A JP61204563 A JP 61204563A JP 20456386 A JP20456386 A JP 20456386A JP H0768484 B2 JPH0768484 B2 JP H0768484B2
Authority
JP
Japan
Prior art keywords
ink
parts
ink composition
marking ink
ascorbic acid
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.)
Expired - Lifetime
Application number
JP61204563A
Other languages
Japanese (ja)
Other versions
JPS6361065A (en
Inventor
雄一 小林
智 斎藤
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.)
Pentel Co Ltd
Original Assignee
Pentel 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 Pentel Co Ltd filed Critical Pentel Co Ltd
Priority to JP61204563A priority Critical patent/JPH0768484B2/en
Publication of JPS6361065A publication Critical patent/JPS6361065A/en
Publication of JPH0768484B2 publication Critical patent/JPH0768484B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明はペン先耐乾燥性に優れたマーキングインキ組成
物に関し,更に詳しくは,長時間キャップをはずしたま
ま放置しておいてもペン先が乾燥しにくいマーキングイ
ンキ組成物に関するものである。
Description: TECHNICAL FIELD The present invention relates to a marking ink composition having excellent resistance to drying at a nib, and more particularly, to a nib that is left uncapped for a long time. Relates to a marking ink composition which is difficult to dry.

(従来の技術) 従来よりマーキングインキ組成物,即ち,油性インキは
被筆記体の限定が少なく,速乾性を有するので広く用い
られており,定着性を有する一般油性インキと剥離性を
有する所謂白板用消去インキとに類別される。
(Prior Art) Conventionally, a marking ink composition, that is, an oil-based ink has been widely used because it has few limitations on the writing material and has a quick-drying property, and a general oil-based ink having a fixing property and a so-called white plate having a peeling property. Erasing ink for use.

(発明が解決しようとする問題点) しかしながら,油性インキは,その速乾性の故に,キャ
ップをはずしたまま放置しておくと溶剤が蒸発し着色材
や樹脂等が析出して,ペン先の表面に樹脂等の皮膜が形
成されカスレを発生したり,はなはだしくは筆記不能と
なってしまうという問題点を有していた。
(Problems to be solved by the invention) However, because the oil-based ink is quick-drying, the solvent evaporates and the coloring material or resin is deposited on the surface of the pen tip if left uncapped. However, there is a problem that a film such as a resin is formed on the surface to cause scratches, or the writing becomes impossible.

(問題点を解決するための手段) そこで本発明者等は,上記問題点を解決すべく鋭意研究
を重ねた結果,遂に本発明を完成したものである。即ち
本発明は,着色材と,有機溶剤と,下記一般式で示され
る化合物とから少なくともなるマーキングインキ組成物
を要旨とする。
(Means for Solving Problems) Therefore, the inventors of the present invention have finally completed the present invention as a result of intensive studies to solve the above problems. That is, the gist of the present invention is a marking ink composition comprising at least a coloring material, an organic solvent, and a compound represented by the following general formula.

(X:アシル基または酸残基または水素を示す) 以下に本発明の各成分について詳細に説明する。 (X: Acyl Group, Acid Residue, or Hydrogen) Each component of the present invention will be described in detail below.

着色材は,染料・顔料を問わない。染料としては,有機
溶剤に可溶な油溶性染料,アルコール可溶性染料を用い
る事ができ,顔料としては,インキ組成中に安定に分散
できるものであれば限定はないが,特に表面を樹脂コー
ティングした所謂加工顔料が分散性,経時安定性,作業
性の点から好ましい。これら着色材の使用量は着色材の
種類や他のインキ成分により異なるが,インキ全量に対
して1〜20重量%,好ましくは2〜17重量%である。
The coloring material may be a dye or a pigment. As the dye, an oil-soluble dye or an alcohol-soluble dye that is soluble in an organic solvent can be used, and the pigment is not limited as long as it can be stably dispersed in the ink composition, but the surface is particularly coated with a resin. So-called processed pigments are preferable in terms of dispersibility, stability over time, and workability. The amount of these colorants used varies depending on the type of colorant and other ink components, but is 1 to 20% by weight, preferably 2 to 17% by weight, based on the total amount of the ink.

有機溶剤としては,エタノール,プロパノール,イソプ
ロパノール,ブタノール等のアルコール類,メチルエチ
ルケトン,メチルイソブチルケトン等のケトン類,酢酸
エチル,酢酸ブチル等のエステル類,ベンゼン,トルエ
ン,キシレン等の芳香族類,エチレングリコールモノエ
チルエーテル等のセロソルブ類,ジエチレングリコール
モノブチルエーテル等のカービトール類等が挙げられ,
これらの一種又は二種以上混合して使用可能である。
Examples of the organic solvent include alcohols such as ethanol, propanol, isopropanol and butanol, ketones such as methyl ethyl ketone and methyl isobutyl ketone, esters such as ethyl acetate and butyl acetate, aromatics such as benzene, toluene and xylene, and ethylene glycol. Cellosolves such as monoethyl ether, carbitols such as diethylene glycol monobutyl ether, and the like,
These can be used alone or in combination of two or more.

これら有機溶剤の使用量はインキ全量に対して55〜90重
量%,好ましくは65〜85重量%である。
The amount of these organic solvents used is 55 to 90% by weight, preferably 65 to 85% by weight, based on the total amount of the ink.

本発明の骨子である前記一般式で示される化合物は,キ
ャップをはずし放置した時の筆跡カスレを防止する為に
使用するものであって,具体的にはアスコルビン酸,ア
スコルビン酸ジパルミテート,アスコルビン酸リン酸エ
ステルマグネシウム塩,アスコルビン酸硫酸エステルニ
ナトリウム塩といったものがあり,その使用量はインキ
全量に対し0.5〜3重量%が望ましい。
The compound represented by the above general formula, which is the skeleton of the present invention, is used for preventing handwriting blur when the cap is removed and left, and specifically, ascorbic acid, ascorbic acid dipalmitate, phosphorus ascorbate. Acid ester magnesium salt and ascorbic acid sulfuric acid ester disodium salt are used, and the amount used is preferably 0.5 to 3% by weight with respect to the total amount of the ink.

以上の成分の他に,定着性を有する一般油性インキとし
ては,皮膜形成能付与,被筆記面への付着性付与及びイ
ンキの粘度調整の為に,従来より用いられている天然樹
脂や合成樹脂−例えば,ロジン系樹脂・セルロース系樹
脂・石油系樹脂・ケトン樹脂・ポリビニルブチラール・
塩化ビニル−酢酸ビニル共重合物の一種又は二種以上混
合し,インキ全量に対して1〜30重量%の使用量で用い
る事が好ましい。又,剥離性を有する所謂白板用消去イ
ンキとしては,上記の成分の他に,前記有機溶剤に可溶
な剥離剤−例えば,高級脂肪酸エステル・高級脂肪族炭
化水素・ポリオキシエチレンアルキエーテル型非イオン
系界面活性剤及びその誘導体・ポリオキシエチレンアル
キルフェノールエーテル型非イオン系界面活性剤−の一
種又は二種以上を混合し,インキ全量に対し1〜10重量
%使用する事が必要である。
In addition to the above components, general oil-based inks that have fixing properties include natural resins and synthetic resins that have been conventionally used in order to impart film-forming ability, adhesion to the writing surface, and viscosity adjustment of ink. -For example, rosin resin, cellulose resin, petroleum resin, ketone resin, polyvinyl butyral,
It is preferable to mix one or more vinyl chloride-vinyl acetate copolymers and use them in an amount of 1 to 30% by weight based on the total amount of the ink. As a so-called white plate erasing ink having a peeling property, in addition to the above-mentioned components, a releasing agent soluble in the organic solvent such as higher fatty acid ester, higher aliphatic hydrocarbon, polyoxyethylene alkether type It is necessary to mix one or more of ionic surfactants and their derivatives and polyoxyethylene alkylphenol ether type nonionic surfactants, and to use 1 to 10% by weight based on the total amount of the ink.

尚,上記成分以外に必要に応じて,防腐・防カビ剤,消
泡剤等の各種添加剤を適宜使用できる。
In addition to the above components, various additives such as antiseptic / antifungal agents and defoaming agents can be appropriately used, if necessary.

本発明のマーキングインキ組成物は公知の混合撹拌機又
は分散機を用い,上記各成分を混合撹拌又は分散するこ
とにより容易に得られる。
The marking ink composition of the present invention can be easily obtained by mixing and stirring or dispersing the above components using a known mixing stirrer or disperser.

(作用) 本発明のマーキングインキ組成物が何故筆跡のカスレを
防止するかは定かでないが以下の様に推察される。
(Function) It is not clear why the marking ink composition of the present invention prevents blurring of handwriting, but it is presumed as follows.

本発明に使用される前記一般式で示される化合物は,ペ
ン先より溶剤が蒸発し着色材や樹脂が析出する際に同時
に析出し,樹脂間の強い結合による皮膜でなく,もろい
皮膜を形成する。そして,この前記一般式で示される化
合物を含んだもろい皮膜は筆記時の圧力で破れるため筆
跡のカスレを防止すると考えられる。
The compound represented by the general formula used in the present invention is simultaneously deposited when the solvent evaporates from the pen tip and the coloring material or resin is deposited, and forms a fragile film instead of a film due to a strong bond between the resins. . It is considered that the fragile film containing the compound represented by the general formula is broken by the pressure during writing, and thus scratches of handwriting are prevented.

(実施例) 以下,本発明を実施例により更に詳細に説明するが,実
施例中単に「部」とあるのは「重量部」を示す。
(Examples) Hereinafter, the present invention will be described in more detail with reference to Examples. In the Examples, "part" means "part by weight".

実施例1(定着性を有するインキ) バリファーストレッド#1808(C.I.アシドレッド混合
物,オリエント化学工業(株)製) 7部 タマノール100S(油溶性フェノール樹脂,荒川化学工業
(株)製 4部 ロジンWW(ロジン樹脂,徳島精油(株)製) 1部 エタノール 64部 エチルセロソルブ 20部 酢酸エチル 3部 L−アスコルビン酸 1部 上記成分をホモミキサーにて2時間撹拌する事により赤
色インキを得た。
Example 1 (ink having fixability) Varifast Red # 1808 (CI Acid Red mixture, manufactured by Orient Chemical Industry Co., Ltd.) 7 parts Tamanol 100S (oil-soluble phenol resin, manufactured by Arakawa Chemical Industry Co., Ltd. 4 parts Rosin WW ( Rosin resin, manufactured by Tokushima Essential Oil Co., Ltd. 1 part Ethanol 64 parts Ethyl cellosolve 20 parts Ethyl acetate 3 parts L-Ascorbic acid 1 part A red ink was obtained by stirring the above components for 2 hours with a homomixer.

実施例2(定着性を有するインキ) ネオザボンブラックRE(C.I.ソルベントブラック27,BAS
F社製) 16 部 ロジンWW 10 部 n−プロパノール 12 部 メチルセロソルブ 60.5部 アスコルビン酸ジパルミテート 1.5部 上記成分を実施例1と同様にして黒色インキを得た。
Example 2 (ink having fixability) Neo Zabone Black RE (CI Solvent Black 27, BAS
(Manufactured by Company F) 16 parts Rosin WW 10 parts n-Propanol 12 parts Methylcellosolve 60.5 parts Ascorbic acid dipalmitate 1.5 parts A black ink was obtained in the same manner as in Example 1.

実施例3(剥離性を有するインキ) フジASブラック(加工顔料,富士色素(株)製) 8 部 エタノール 45 部 イソプロパノール 35.4部 L−アスコルビン酸 1 部 2−エチルヘキサン酸ヘキサデシル 6.8部 エマルゲン408(ポリオキシエチレンオレイルエーテ
ル,花王石鹸(株)製) 3.8部 上記成分を実施例1と同様にして黒色インキを得た。
Example 3 (ink having releasability) Fuji AS black (processed pigment, manufactured by Fuji Dye Co., Ltd.) 8 parts Ethanol 45 parts Isopropanol 35.4 parts L-Ascorbic acid 1 part Hexadecyl 2-ethylhexanoate 6.8 parts Emulgen 408 (Poly) Oxyethylene oleyl ether, manufactured by Kao Soap Co., Ltd. 3.8 parts A black ink was obtained in the same manner as in Example 1.

実施例4(剥離性を有するインキ) フジIKブルー(加工顔料,富士色素(株)製) 7 部 酢酸ブチル 30 部 メチルエチルケトン 43.5部 メチルイソブチルケトン 7 部 アスコルビン酸ジパルミテート 1.5部 n−ブチルステアレート 8 部 流動パラフィン 3 部 上記成分を実施例1と同様にして青色インキを得た。Example 4 (ink having releasability) Fuji IK Blue (processed pigment, manufactured by Fuji Dye Co., Ltd.) 7 parts Butyl acetate 30 parts Methyl ethyl ketone 43.5 parts Methyl isobutyl ketone 7 parts Ascorbic acid dipalmitate 1.5 parts n-Butyl stearate 8 parts Liquid paraffin 3 parts A blue ink was obtained in the same manner as in Example 1 except that the above components were used.

比較例1 実施例1よりL−アスコルビン酸を抜き,その分エチル
セロソルブを加え実施例1と同様にして赤色インキを得
た。
Comparative Example 1 A red ink was obtained in the same manner as in Example 1 except that L-ascorbic acid was removed from Example 1 and ethyl cellosolve was added.

比較例2 実施例2よりアスコルビン酸ジパルミテートを抜き,そ
の分n−プロパノールを加え実施例1と同様にして黒色
インキを得た。
Comparative Example 2 A black ink was obtained in the same manner as in Example 1 except that ascorbic acid dipalmitate was removed from Example 2 and n-propanol was added accordingly.

比較例3 実施例3よりL−アスコルビン酸を抜き,その分イソプ
ロパノールを加え実施例1と同様にして黒色インキを得
た。
Comparative Example 3 A black ink was obtained in the same manner as in Example 1 except that L-ascorbic acid was removed from Example 3 and isopropanol was added.

比較例4 実施例4よりアスコルビン酸ジパルミテートを抜き,そ
の分酢酸ブチルを加え実施例1と同様にして黒色インキ
を得た。
Comparative Example 4 A black ink was obtained in the same manner as in Example 1 except that ascorbic acid dipalmitate was removed from Example 4 and butyl acetate was added accordingly.

以上,実施例1〜4及び比較例1〜4で得たマーキング
インキ組成物を使用してペン先耐乾燥性試験を行なった
結果を表に示す。
The results of the pen tip drying resistance test using the marking ink compositions obtained in Examples 1 to 4 and Comparative Examples 1 to 4 are shown in the table.

(効果) 以上の如く,本発明のマーキングインキ組成物は,キャ
ップを取りはずし放置した時に筆跡のカスレが発生する
迄の時間が長く実用性に優れたものである。
(Effects) As described above, the marking ink composition of the present invention is excellent in practicality because it takes a long time until blurring of handwriting occurs when the cap is removed and left to stand.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】着色材と,有機溶剤と,下記一般式で示さ
れる化合物とから少なくともなるマーキングインキ組成
物。 (X:アシル基または酸残基または水素を示す)
1. A marking ink composition comprising at least a coloring material, an organic solvent, and a compound represented by the following general formula. (X: represents an acyl group, an acid residue, or hydrogen)
JP61204563A 1986-08-30 1986-08-30 Marking ink composition Expired - Lifetime JPH0768484B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61204563A JPH0768484B2 (en) 1986-08-30 1986-08-30 Marking ink composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61204563A JPH0768484B2 (en) 1986-08-30 1986-08-30 Marking ink composition

Publications (2)

Publication Number Publication Date
JPS6361065A JPS6361065A (en) 1988-03-17
JPH0768484B2 true JPH0768484B2 (en) 1995-07-26

Family

ID=16492541

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61204563A Expired - Lifetime JPH0768484B2 (en) 1986-08-30 1986-08-30 Marking ink composition

Country Status (1)

Country Link
JP (1) JPH0768484B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8007096B2 (en) 2003-10-29 2011-08-30 Hewlett-Packard Development Company, L.P. Ink compositions for use in highlighter markers and associated methods

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5879067A (en) * 1981-11-04 1983-05-12 Sakura Color Prod Corp Ink composition for marking pen
JPS5961778A (en) * 1982-09-30 1984-04-09 Toppan Printing Co Ltd Ink composition for detecting oxygen and preservation thereof

Also Published As

Publication number Publication date
JPS6361065A (en) 1988-03-17

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