JPS62199498A - Eraser for erasing water-color ink - Google Patents

Eraser for erasing water-color ink

Info

Publication number
JPS62199498A
JPS62199498A JP4297186A JP4297186A JPS62199498A JP S62199498 A JPS62199498 A JP S62199498A JP 4297186 A JP4297186 A JP 4297186A JP 4297186 A JP4297186 A JP 4297186A JP S62199498 A JPS62199498 A JP S62199498A
Authority
JP
Japan
Prior art keywords
eraser
water
handwriting
parts
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.)
Granted
Application number
JP4297186A
Other languages
Japanese (ja)
Other versions
JPH0635236B2 (en
Inventor
安宏 高橋
好人 今泉
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 JP4297186A priority Critical patent/JPH0635236B2/en
Publication of JPS62199498A publication Critical patent/JPS62199498A/en
Publication of JPH0635236B2 publication Critical patent/JPH0635236B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明ハ、トレーシングペーパー、マット加工フィルム
等の非浸透面に描かれた水性インキによる筆跡を消去す
るための水性インキ消去用消しゴムに関するものである
Detailed Description of the Invention (Field of Industrial Application) The present invention (c) relates to a water-based ink erasing eraser for erasing handwriting drawn on water-based ink on non-penetrating surfaces such as tracing paper and matte processed films. It is.

(従来の技術゛とその問題点) 従来、トレーシングペーハー、マット加工フイルム等の
非浸透面に筆記するだめの水性インキについては、筆跡
に耐水性を付与するためにインキのバインダーとしてア
ルカリ水可溶型の樹脂を添加したものが知られている。
(Conventional technology and its problems) Conventionally, with respect to water-based inks used for writing on non-permeable surfaces such as tracing paper and matte processed films, alkaline water was used as a binder for the ink in order to impart water resistance to handwriting. It is known that a melt-type resin is added.

この種水性インキによる筆跡を消去する方法としては、
上記水性インキ中のバインダー樹脂を膨潤、溶解し得る
溶剤を消しゴム中に含有せしめ、これによって擦過に伴
いその筆跡を膨潤溶解して除去するタイプのものが知ら
れている。
As a method for erasing handwriting made with this type of water-based ink,
A type of eraser is known in which a solvent that can swell and dissolve the binder resin in the aqueous ink is contained in the eraser, and the eraser swells and dissolves handwriting as it is rubbed, thereby removing it.

然るに、かかる方法によると、筆跡消去箇所に再筆記を
行なった場合、被筆記面であるトレーシングペーハー、
フィルムによっては再筆記シた筆跡かにじんでしまうと
いう問題を有していた。
However, according to this method, when rewriting is performed on the erased part of the handwriting, the tracing paper, which is the writing surface,
Depending on the film, there was a problem in that the handwriting that was rewritten would smudge.

本発明者らは、これらの再筆記による筆跡にじみについ
てその原因を追究すべく検討したところ、筆跡がフィル
ム面に奇麗にのるようにフィルム面の濡れ性が水性イン
キに対して良好となされており、消去後筆跡消去箇所に
は僅かながら水性インキ中のバインダー樹脂を膨潤、溶
解する溶剤が残されており、濡れ性を良好とされたフィ
ルム面等は却りて残存する溶剤によって濡れ性が異常に
良くなり、この為再筆記の際の水性インキがフィルム上
で四方に拡散してしまい、その結果として筆跡かにじむ
ものであるとの知見を得るに至った。
The inventors of the present invention investigated the cause of handwriting smearing caused by rewriting, and found that the wettability of the film surface is good for water-based ink so that handwriting can be placed neatly on the film surface. However, after erasing handwriting, a small amount of solvent that swells and dissolves the binder resin in the water-based ink remains in the erased area, and the film surface, which is supposed to have good wettability, actually has poor wettability due to the remaining solvent. It was found that the water-based ink during re-writing spreads in all directions on the film, and as a result, the handwriting bleeds.

(問題点を解決するための手段) 本発明は以上の知見に鑑みなされたもので。(Means for solving problems) The present invention was made in view of the above findings.

筆跡消去箇所における再筆記によるにじみを防止すべく
、その消しゴムへの添加剤について種々検討を重ねたと
ころ、消しゴム中に特定の有機酸を含有せしめたものが
良好であることを見い出し、遂に完成したものである。
In order to prevent smearing caused by re-writing on erased areas, we conducted various studies on additives to the eraser, and found that an eraser containing a specific organic acid was effective, and we finally completed the process. It is something.

即ち本発明は、水性インキのバインダー樹脂を膨潤また
は溶解させる溶剤を含有せろ水性インキ消去用消しゴム
において、該消しゴム中にその沸点が150℃以上であ
るかもしくはその分解温度が150℃以上であり、且つ
、これらの溶解度が0.1f/10”OP水(20℃)
以上である有機酸を含有することを特徴とする水性イン
キ消去用消しゴムを要旨とするものである。
That is, the present invention provides an eraser for erasing water-based ink containing a solvent that swells or dissolves the binder resin of water-based ink, the eraser having a boiling point of 150°C or higher or a decomposition temperature of 150°C or higher, Moreover, the solubility of these is 0.1f/10” OP water (20℃)
The object of the present invention is to provide an eraser for erasing water-based ink, which is characterized by containing the above organic acid.

以下2本発明を詳述する。Two aspects of the present invention will be described in detail below.

本発明における水性インキ中のバインダー樹脂を膨潤ま
たは溶解させる溶剤としては、エチレングリコール、ジ
エチレングリコール、トリエチレングリコール、グロピ
レンクリコール。
Examples of the solvent for swelling or dissolving the binder resin in the aqueous ink of the present invention include ethylene glycol, diethylene glycol, triethylene glycol, and glopylene glycol.

ジプロピレングリコール等のグリコール類が挙げられる
。これらの溶剤は1種もしくは2種以上適宜混合して使
用され、その使用量は消しゴム全重量に対して5〜50
重量%、好ましくは5〜30重量%となる。
Examples include glycols such as dipropylene glycol. These solvents are used alone or in a mixture of two or more, and the amount used is 5 to 50% based on the total weight of the eraser.
% by weight, preferably 5 to 30% by weight.

本発明の特徴点でもあるにじみ防止剤としての機能をも
った有機酸は、上記した溶剤中に溶解されて使用される
か、もしくは直接消しゴム基材中に添加されて使用され
るもので筆跡消去後は、フィルム上にこの有機酸が溶剤
と共に僅かに残っているものである。従って、基本的に
は、筆跡消去箇所に新たな水性インキが接した際、この
インキ中に前記残存せる有機酸が溶は込み、インキを酸
性にするため、その部分のインキ中のアルカリ水可溶型
樹脂が析出してインキが増粘し、その結果再筆記の際の
筆跡が四方に拡散することなく、にじみが防止されるも
のと思われる。
The organic acid that functions as a smear-preventing agent, which is a feature of the present invention, can be used dissolved in the above-mentioned solvent or directly added to the eraser base material to erase handwriting. After that, a small amount of this organic acid remains on the film together with the solvent. Therefore, basically, when a new water-based ink comes into contact with the area where handwriting has been erased, the remaining organic acid dissolves into this ink and makes the ink acidic, so that the alkaline water in the ink at that area is absorbed. It is thought that the molten resin precipitates and the ink thickens, and as a result, the handwriting does not spread in all directions when rewritten, and bleeding is prevented.

よってこの有機酸は、水性インキ中に速やかに溶解せね
ばならないため、水100!に対する溶解度は0.17
 (20℃)以上であることが必要となる。その溶解度
が0.1ノ未満であると再筆記による筆跡かにじむ恐れ
があるためである。更に、この有機酸について説明すれ
ば、その沸点が150℃以上であるかもしくはその分解
温度が150℃以上である必要がある。何故ならば、実
際に消しゴムを得る際、その成形温度については約11
0℃位を必要とし、前述せる沸点もしくは分解温度の条
件が満足されていないとこの有機酸が添加量目体少量で
あることより蒸発したり2分解したりして所期の目的が
達成不能となるためである。従って、これらの条件を満
足し得る有機酸としては以下の様なものが挙げられる。
Therefore, this organic acid must be dissolved quickly in the water-based ink, so the organic acid must be dissolved quickly in the water-based ink. Solubility in is 0.17
(20°C) or higher. This is because if the solubility is less than 0.1, handwriting may bleed when rewritten. Furthermore, this organic acid needs to have a boiling point of 150°C or higher or a decomposition temperature of 150°C or higher. This is because when actually obtaining an eraser, the molding temperature is approximately 11
If the boiling point or decomposition temperature conditions described above are not met, the organic acid will evaporate or decompose due to the relatively small amount added, making it impossible to achieve the intended purpose. This is because. Therefore, examples of organic acids that can satisfy these conditions include the following.

即チ、シクロヘキサンカルボン酸、コノ・り酸。Sokuthi, cyclohexanecarboxylic acid, cono-phosphoric acid.

アジピン酸、安息香酸等については、そのものが分解す
る以前に蒸発するタイプの有機酸であるためその沸点を
もって特定されるものであり。
Adipic acid, benzoic acid, etc. are organic acids that evaporate before being decomposed, so they are identified by their boiling points.

tたクエン酸については、蒸発する以前にそのものの分
解が行なわれるタイプの有機酸であるためその分解温度
をもって特定されるものである。とりわけクエン酸につ
いては上表に示す如〈その溶解度が極めて高いものであ
るたメ、水性インキに対する溶解性も著しく良好となり
Citric acid is a type of organic acid that decomposes itself before it evaporates, so it is specified by its decomposition temperature. In particular, as shown in the table above, citric acid has an extremely high solubility, and its solubility in water-based inks is also extremely good.

これ故短時間で水性インキを酸性と化し、再筆記の際の
筆跡にじみ防止効果の点で非常に有利なものとなる。以
上の有機酸は1種もしくは2種以上適宜混合して使用さ
れ、その使用量は。
Therefore, the water-based ink becomes acidic in a short period of time, which is very advantageous in preventing handwriting from smearing when rewriting. The above organic acids may be used alone or in an appropriate mixture of two or more, and the amount used is as follows.

水性インキ中のバインダー樹脂を膨潤または溶解する溶
剤の量に対して1〜20重量%好ましくは5〜15重量
%となる。
The amount is 1 to 20% by weight, preferably 5 to 15% by weight, based on the amount of solvent that swells or dissolves the binder resin in the aqueous ink.

次に本発明の消しゴムの製造方法について述べる。Next, the method for manufacturing the eraser of the present invention will be described.

有機酸及び水性インキのバインダー樹脂を膨潤または溶
解させる溶剤を実際に消しゴム中に含有せしめる方法に
ついては種々譲るが、以下、にその代表的な例を2つ挙
げて説明する。即ち。
There are various methods for actually incorporating into the eraser a solvent that swells or dissolves the organic acid and the binder resin of the aqueous ink, but two typical examples will be described below. That is.

■可塑剤をゲル化剤でゲル化した後、これに有機酸と溶
剤と従来より知られている消しゴム基材、特に好ましく
はポリ塩化ビニルまたはポリ塩化ビニルとポリ酢酸ビニ
ルとの共重合体と安定剤を加えて均一に分散混合してペ
ースト状物とした後、加熱成形して消しゴムを得る方法
■ After gelling the plasticizer with a gelling agent, this is mixed with an organic acid, a solvent, and a conventionally known eraser base material, particularly preferably polyvinyl chloride or a copolymer of polyvinyl chloride and polyvinyl acetate. A method to obtain an eraser by adding a stabilizer and uniformly dispersing and mixing it to form a paste, which is then heated and molded.

■前記せる消しゴム基材に可塑剤、安定剤を加えてペー
スト状物とした後に、これに有機酸と溶剤を芯物質とす
る粉末法マイクロカプセルを加えて均一に攪拌分散し、
その後これを加熱成形して消しゴムを得る方法。
■After adding a plasticizer and a stabilizer to the above-mentioned eraser base material to form a paste, powder method microcapsules containing an organic acid and a solvent as core materials are added and uniformly stirred and dispersed.
This is then heated and molded to obtain an eraser.

である。It is.

而して本発明においては2以上の各方法によって所望の
消しゴムを得るもので、有機酸については適宜これを溶
剤に溶解せしめて使用してもよく、また、必要に応じて
各種充填剤、香料高吸水性高分子物質等を添加し得るこ
と勿論である。
Accordingly, in the present invention, the desired eraser is obtained by two or more methods, and the organic acid may be dissolved in a solvent as appropriate, and various fillers and fragrances may be added as necessary. It goes without saying that superabsorbent polymer substances and the like may be added.

(実施例) 以下2本発明を実施例に基づき更に詳細に説明する。(Example) The present invention will be explained in more detail below based on two examples.

実施例1 ジオクチルフタレート(可塑剤)150重量部(以下、
単に「部」と表わす。)にゲル化剤(ゲルオールD、新
日本理科■製)5部を加えて加熱溶解した後、放冷して
可塑剤のゲル化物155部を得た。このゲル化物に、ジ
エチレングリコール55部と。
Example 1 150 parts by weight of dioctyl phthalate (plasticizer) (hereinafter referred to as
It is simply expressed as "part." ) was added with 5 parts of a gelling agent (Gel All D, manufactured by Shin Nippon Rika ■), heated and dissolved, and then allowed to cool to obtain 155 parts of a gelled plasticizer. Add 55 parts of diethylene glycol to this gelled product.

・ポリ塩化ビニ/’ (G e o n 121 。・Polyvinyl chloride/' (G e o n 121.

日本ゼオン■製)        150部・エポキシ
化大豆油(安定剤)     3部・炭酸カルシウム 
         30部・シクロヘキサンカルボン酸
      6部を加え、均一に攪拌混合した後、11
0℃220分間でプレス成形を行い消しゴムを得た。
Nippon Zeon ■) 150 parts epoxidized soybean oil (stabilizer) 3 parts calcium carbonate
Add 30 parts of cyclohexanecarboxylic acid and 6 parts of cyclohexanecarboxylic acid, stir and mix evenly, and add 11 parts of cyclohexane carboxylic acid.
Press molding was performed at 0°C for 220 minutes to obtain an eraser.

実施例2 〈粉床法マイクロカプセルの製法〉 プロピレングリコール70部にクエン酸7部を浴解し、
これに炭酸カルシウム45部を攪拌混合してペースト状
物122部を得2次いでこれを超微粉末シリカ粉20部
中で高速攪拌してシリカ壁マイ′クロカプセル142部
を得た。
Example 2 <Production method of powder bed microcapsules> 7 parts of citric acid was dissolved in 70 parts of propylene glycol,
45 parts of calcium carbonate were mixed with stirring to obtain 122 parts of a paste-like product. This was then stirred at high speed in 20 parts of ultrafine silica powder to obtain 142 parts of silica-walled microcapsules.

く消しゴムの製法〉 ―ポリ塩化ビニル(Geon  121゜日本ゼオン■
製)       150部・ジオクチルフタレート(
可塑剤)150部・エポキシ化大豆油(安定剤)   
 3部上上記弁を攪拌混合してペースト状物303部を
得、このペースト状物に上述のマイクロカプセル142
部を加えて攪拌混合した後、110”C,20分間でプ
レス成形を行い消しゴムを得た。
Manufacturing method of eraser - Polyvinyl chloride (Geon 121゜Nippon Zeon ■
) 150 parts dioctyl phthalate (
Plasticizer) 150 parts/Epoxidized soybean oil (stabilizer)
3 parts of the above valve were stirred and mixed to obtain 303 parts of a paste-like material, and the above-mentioned microcapsules 142 were added to this paste-like material.
After stirring and mixing, press molding was performed at 110''C for 20 minutes to obtain an eraser.

比較例1,2 上記実施例1.2において、夫々有機酸を除去した以外
は全て実施例1,2と同様になしたものを比較例1,2
とした。
Comparative Examples 1 and 2 Comparative Examples 1 and 2 were prepared in the same manner as in Examples 1 and 2, except that the organic acids were removed, respectively.
And so.

(効果) フィルム(B15hop  Graphics  In
c社製)上に描かれた水性顔料インキ(ロットリングF
、ロットリング社展)による追跡を上記実施例1,2及
び比較例1,2で得られた消しゴムで夫々擦過消去し、
この後、この筆跡消去箇所に同インキを用いて再筆記を
行なったところ、実施例1.2の消しゴムによるものに
ついては筆跡のにじみがみられず、比較例1,2の消し
ゴムによるものについては筆跡のにじみがみられた。
(Effect) Film (B15hop Graphics In
Water-based pigment ink (manufactured by Rotring F)
, Rotring Exhibition) were rubbed and erased using the erasers obtained in Examples 1 and 2 and Comparative Examples 1 and 2, respectively.
After that, when the same ink was used to rewrite the erased handwriting, no smearing of the handwriting was observed when using the eraser of Example 1.2, and when using the eraser of Comparative Examples 1 and 2, no bleeding was observed. Smudged handwriting was visible.

この様に本発明の水性インキ消去用消しゴムによれば、
筆跡消去箇所における再筆記時のにじみが極力防止でき
実用上きわめて有利なものである。
As described above, according to the water-based ink erasing eraser of the present invention,
This is extremely advantageous in practice because it can prevent blurring when rewriting at the erased handwriting location as much as possible.

Claims (1)

【特許請求の範囲】[Claims] 水性インキのバインダー樹脂を膨潤または溶剤させる溶
剤を含有せる水性インキ消去用消しゴムにおいて、該消
しゴム中にその沸点が150℃以上であるかもしくはそ
の分解温度が150℃以上であり、且つ、これらの溶解
度が0.1g/100g水(20℃)以上である有機酸
を含有することを特徴とする水性インキ消去用消しゴム
In an eraser for erasing water-based ink containing a solvent that swells or dissolves the binder resin of water-based ink, the eraser has a boiling point of 150°C or higher, or a decomposition temperature of 150°C or higher, and the solubility of these solvents. An eraser for erasing water-based ink, characterized in that it contains an organic acid having a ratio of 0.1 g/100 g water (20° C.) or more.
JP4297186A 1986-02-28 1986-02-28 Eraser for erasing water-based ink Expired - Lifetime JPH0635236B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4297186A JPH0635236B2 (en) 1986-02-28 1986-02-28 Eraser for erasing water-based ink

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4297186A JPH0635236B2 (en) 1986-02-28 1986-02-28 Eraser for erasing water-based ink

Publications (2)

Publication Number Publication Date
JPS62199498A true JPS62199498A (en) 1987-09-03
JPH0635236B2 JPH0635236B2 (en) 1994-05-11

Family

ID=12650922

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4297186A Expired - Lifetime JPH0635236B2 (en) 1986-02-28 1986-02-28 Eraser for erasing water-based ink

Country Status (1)

Country Link
JP (1) JPH0635236B2 (en)

Also Published As

Publication number Publication date
JPH0635236B2 (en) 1994-05-11

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