JPS60101098A - Eraser for correcting electrostatic copying picture - Google Patents

Eraser for correcting electrostatic copying picture

Info

Publication number
JPS60101098A
JPS60101098A JP20886283A JP20886283A JPS60101098A JP S60101098 A JPS60101098 A JP S60101098A JP 20886283 A JP20886283 A JP 20886283A JP 20886283 A JP20886283 A JP 20886283A JP S60101098 A JPS60101098 A JP S60101098A
Authority
JP
Japan
Prior art keywords
eraser
solvent
parts
electrostatic copying
toner
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
JP20886283A
Other languages
Japanese (ja)
Other versions
JPH0225800B2 (en
Inventor
安宏 高橋
鋭一 岡部
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 JP20886283A priority Critical patent/JPS60101098A/en
Publication of JPS60101098A publication Critical patent/JPS60101098A/en
Publication of JPH0225800B2 publication Critical patent/JPH0225800B2/ja
Granted 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】 本発明は静電複写法によシ形成された画像を修正する為
の消しゴムに関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an eraser for correcting images formed by electrostatography.

近年、静電複写法が工業図面の作成に用いられるように
なり、使用される紙の中でも、特にトレーシングペーパ
ーの様な透明性の高い紙に画像を形成させたり、また製
図用フィルムに画像を形成させた第2原図としての用途
が増大している。
In recent years, electrostatic copying has come to be used to create industrial drawings, and among the papers used, it is used to form images on highly transparent papers such as tracing paper, and to form images on drafting film. Its use as a second original drawing is increasing.

静電複写法でトレーンングペーパー等普通紙および製図
用フィルムに画像を形成せしめた。
Images were formed on plain paper such as training paper and drafting film by electrostatic copying.

いわゆる第2原図は2画像がトナーと称される着色合成
樹脂粉末の溶融固着したもので構成されている為、単な
る消しゴム修正では修正出来ない場合が多い。
Since the so-called second original image is composed of two images that are fused and fixed together with colored synthetic resin powder called toner, it is often impossible to correct it by simply using an eraser.

従来、このような第2原図の修正は、トナーの溶剤を画
像の修正部に直接塗布し、トナーを溶解した後、これを
拭取るといった方法が取られていた。
Conventionally, such correction of the second original image has been carried out by applying a toner solvent directly to the corrected portion of the image, dissolving the toner, and then wiping it off.

トナーの溶剤としてはトナーを良く溶かす。As a toner solvent, it dissolves toner well.

ベンゼン、トルエン、キシレ/などの芳香族炭化水素や
トナーの溶融固着剤としてのトリクロルエチレンなどの
塩化炭化水素、また、これらの他にも、エステル類、ケ
トン類、脂肪族炭化水素等を単独又は適当に混合して使
用している。
Aromatic hydrocarbons such as benzene, toluene, xylene, etc., chlorinated hydrocarbons such as trichlorethylene as a toner melt fixing agent, and in addition to these, esters, ketones, aliphatic hydrocarbons, etc. Mix and use appropriately.

しかし、この方法の場合、トナーを溶解した後、拭取る
為、溶解性の良い溶剤はど1紙面。
However, in this method, after the toner is dissolved, it is wiped off, so a solvent with good solubility is only used on the paper.

フィルム面を汚す傾向を有している。It has a tendency to stain the film surface.

また、汚れを少なくする為に、水又は低級アルコールと
これと相溶性のあるケトン類、エーテル類、エステル類
を混合した。溶剤を使用した(特公昭4B−55420
号)例等があるが。
In addition, in order to reduce staining, water or lower alcohols were mixed with ketones, ethers, and esters that are compatible with water or lower alcohols. Using a solvent (Special Publication No. 4B-55420
No.) There are examples.

修正後の乾燥時間を短かくする為に低沸点、揮発性溶剤
が使用されている。この為、修正操作を迅速に行わねば
ならず、簡単な修正法とは言えなかった3゜ さらに2画像に直接、溶剤を塗布する為、繊維の密でな
い紙については、溶解したトナーが −紙の繊維の中に
浸透してしまい修正が不可能であった。
Low boiling point, volatile solvents are used to shorten the drying time after correction. For this reason, the correction operation had to be carried out quickly, and it was not an easy correction method. 3. In addition, since the solvent is applied directly to the two images, the dissolved toner may be removed from the paper if the fibers are not dense. It penetrated into the fibers of the fibers and was impossible to repair.

、本発明者等は、トナーの溶剤を消しゴム中に含有せし
めることが出来れば、上述せる問題点が解消されるとの
見地に立ち、鋭意研究の結果。
The inventors of the present invention have conducted intensive research based on the viewpoint that the above-mentioned problems can be solved if the toner solvent can be contained in the eraser.

遂に本発明を完成したものである。This invention has finally been completed.

即ち2本発明は、下記条件を有する沸点120℃以上の
溶剤を消しゴム中に含有せしめた静電複写画像修正用消
しゴムを要旨とするものである9、 〈条件〉 水素結合力が弱の時 溶解性パラメーター(j)が7、
0〜11.1 (caJ/c/)”水素結合力が中の時
 溶解性パラメーター(i)が7、4〜14.7 (c
at ld )”本発明は、トナーの溶剤を消しゴム中
に含有せしめたので溶剤が直接紙面、フィルム面に接し
ないので1紙面、フィルム面を汚すことがなく、又、繊
維が密でない紙でも修正を可能としたものである。
That is, 2. The gist of the present invention is an eraser for electrostatic copy image correction, which contains a solvent with a boiling point of 120° C. or higher having the following conditions.9. Conditions: When the hydrogen bonding force is weak: Dissolution The gender parameter (j) is 7,
0 to 11.1 (caJ/c/)" When the hydrogen bond strength is medium, the solubility parameter (i) is 7, 4 to 14.7 (c
In the present invention, since the toner solvent is contained in the eraser, the solvent does not come into direct contact with the paper or film surface, so it does not stain the paper or film surface, and it can also be corrected even on paper where the fibers are not dense. This made it possible.

以下2本発明の詳細な説明する。Two aspects of the present invention will be described in detail below.

消しゴム中に含有される溶剤としてはトナーを溶解する
溶剤で、消しゴム原材料中に分散して加熱成型する事よ
り沸点が120℃以上望ましくは200℃以上のもので
あれば良い。
The solvent contained in the eraser may be any solvent that dissolves the toner and has a boiling point of 120° C. or more, preferably 200° C. or more, since it can be dispersed in the eraser raw material and heated and molded.

又、トナーのバインダーの主な樹脂であるポリスチレ/
の溶解パラメーターはメーカー、グレードにより多少異
なるが、その値は、水素結合力が(弱)で7.0〜11
.1 (L ca1101工&−)。
In addition, polystyrene, which is the main resin of toner binder,
The solubility parameters of 2020 differ slightly depending on the manufacturer and grade, but the values are 7.0 to 11 for (weak) hydrogen bonding strength.
.. 1 (L ca1101 engineering &-).

(中)で7.4〜14.7 (Lcalldゴ&−)テ
ある。
(Medium) and 7.4 to 14.7 (Lcalld go&-)te.

更に、グレード、コポリマーによっては、水素結合力(
強)で9.5〜14.5 (II cat!/a/、]
−’) (D値を持つものもある。
Furthermore, depending on the grade and copolymer, hydrogen bonding strength (
Strong) 9.5 to 14.5 (II cat!/a/,]
-') (Some have D value.

この為、消しゴムに含有される溶剤としては。For this reason, as a solvent contained in erasers.

トナーを溶解させる条件として溶解パラメーターが水素
結合力が(弱)でZO〜11.1.(中)でZ4〜14
.5のもので、かつ、消しゴム原材料中に分散して、加
熱成型するため、上述した沸点が120℃以上、好まし
くは200C以上のものとなる。
The conditions for dissolving the toner are as follows: the dissolution parameters are hydrogen bond strength (weak) and ZO~11.1. (Middle) Z4-14
.. 5, and because it is dispersed in the eraser raw material and heated and molded, the boiling point mentioned above is 120° C. or higher, preferably 200° C. or higher.

上述の溶剤の具体例を次表に示す。Specific examples of the above-mentioned solvents are shown in the following table.

これらの溶剤は単独もしくは2種以上の混合物として使
用できる。尚、使用できる溶剤としては、上記のものに
限らない。
These solvents can be used alone or as a mixture of two or more. Note that the solvents that can be used are not limited to those mentioned above.

溶剤の使用量としては消しゴム全量に対して5〜50重
量係、好ましくは5〜30重量%である。
The amount of solvent used is 5 to 50% by weight, preferably 5 to 30% by weight, based on the total amount of the eraser.

次に溶剤を消しゴム中に含有させる形態としては、溶剤
を芯物質としたマイクロカプセルとして含有させるか、
溶剤を吸着させた多孔性粉体として含有させる形態が考
えられる。
Next, the solvent can be contained in the eraser in the form of microcapsules with the solvent as a core material, or
A conceivable form is to contain it as a porous powder adsorbed with a solvent.

、前者は、経時的な性能の劣化が少ないというメリット
がある。マイクロカプセルの製法としテハ、コアセルベ
ーション法+ s床i、in 5itu重合法、界面沈
澱法など従来公知の方法が採用で色、消しゴムを使用中
の圧力により容易にマイクロカブキルが破壊されるもの
であればよい。
, the former has the advantage of less deterioration of performance over time. The microcapsules are produced using conventionally known methods such as Teha, coacervation method + s-bed method, in-5-itu polymerization method, and interfacial precipitation method. It is fine as long as it is something.

又、後者は経時的な性能は前者に較べてやや劣るものの
、製造の容易性、低コストで製造できるというメリット
がある。
Furthermore, although the latter has slightly inferior performance over time compared to the former, it has the advantage of being easier to manufacture and can be manufactured at low cost.

多孔性粉体としては、吸泥量の比較的多い無機又は有機
物から適宜選択して使用すればよく。
The porous powder may be appropriately selected from inorganic or organic materials that absorb a relatively large amount of mud.

具体例としては、活性アルミナ、タルク、ベントナイト
、炭酸カルシウム、活性白土、多孔質樹脂粉体などが挙
げられる。
Specific examples include activated alumina, talc, bentonite, calcium carbonate, activated clay, and porous resin powder.

尚、マイクロカプセル材(壁物質)並びに多孔性粉体と
溶剤の使用量は、マイクロカプセル材、多孔性粉体の種
類によって必ずしも一様ではないが、マイクロカプセル
材並びに多孔性粉体に比し、溶剤が少なすぎる場合には
、消去性の効果が少なく、又、多すぎる場合には、溶剤
が消しゴム中に浸み出したり、或いは消しゴム表面に移
行したりする事があり、マイクロ1.カプセル材並びに
多孔性粉体と溶剤との比(重量)を1 : 0.4〜1
:10の範囲に設定することが好ましい。
Note that the amounts of microcapsule material (wall material), porous powder, and solvent used are not necessarily uniform depending on the type of microcapsule material and porous powder, but compared to the microcapsule material and porous powder, If the amount of solvent is too small, the erasing effect will be small, and if it is too large, the solvent may seep into the eraser or migrate to the surface of the eraser. The ratio (weight) of the capsule material and porous powder to the solvent is 1:0.4 to 1.
: It is preferable to set it in the range of 10.

次に消しゴムの製造方法について簡単に述べる。Next, the method for manufacturing the eraser will be briefly described.

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、ポリ塩化ビニルとボてペースト状物とし
た。
A conventionally known eraser base material, particularly preferably polyvinyl chloride or polyvinyl chloride, is used as a paste-like product.

このペースト状物に前述したマイクロカプセル及び/又
は多孔性粉体を加え、均一に分散させた後、加熱成型し
て消しゴムとすればよい。
The above-mentioned microcapsules and/or porous powder may be added to this paste-like material, uniformly dispersed, and then heated and molded to form an eraser.

上述した本発明の消しゴムは、マイクロカプセル及び/
又は多孔性粉体にトナー溶剤を保持させたため、経時的
に安定で、かつ消去時に紙面、フィルム面を汚すことな
く、繊維の密でない紙でもトナーを溶解した溶剤を消し
屑により吸着せしめることができるので、トナーを溶解
した溶剤が紙に浸透することがなく、消去修正が可能と
なっだ。
The eraser of the present invention described above contains microcapsules and/or
Or, since the toner solvent is held in the porous powder, it is stable over time and does not stain the paper surface or film surface during erasing, and the solvent in which the toner is dissolved can be adsorbed by the eraser waste even on paper with less dense fibers. As a result, the solvent used to dissolve the toner does not penetrate into the paper, making it possible to erase and correct the paper.

以下、実施例に基づき本発明の詳細な説明する。尚、実
施例中1部」とあるのは「重量部」を示す。
Hereinafter, the present invention will be explained in detail based on Examples. In the examples, "1 part" indicates "part by weight."

実施例1 (マイクロカプセルの製法、粉床法) 2−フェノキンエタノール105部と炭酸カル/ウム7
5部を攪拌混合して、ペースト180部を得る。
Example 1 (Production method of microcapsules, powder bed method) 105 parts of 2-phenoquine ethanol and 7 parts of calcium carbonate
5 parts were stirred and mixed to obtain 180 parts of paste.

これを超微粉末シリカ粉30部で高速攪拌してシリカ壁
マイクロカプセルヲ得り。
This was stirred at high speed with 30 parts of ultrafine silica powder to obtain silica wall microcapsules.

(消しゴムの製法) ポリ塩化ビニル(日本ゼオン■製。(Eraser manufacturing method) Polyvinyl chloride (manufactured by Nippon Zeon ■).

Gcon21 ) 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 炭酸カルシウム(充填剤) 10部 上記成分を攪拌混合して、塩ビペーストを得た。
Gcon21) 150 parts dioctyl phthalate (plasticizer) 150 parts epoxidized soybean oil (stabilizer) 3 parts calcium carbonate (filler) 10 parts The above components were stirred and mixed to obtain a vinyl chloride paste.

この塩ヒヘースト616部に上述のカプセル210部を
加え、攪拌混合した後、110℃。
210 parts of the above-mentioned capsules were added to 616 parts of this salted hechaste, mixed with stirring, and heated to 110°C.

20分間、プレス成型して消しゴムを得た。An eraser was obtained by press molding for 20 minutes.

実施例2 (マイクロカプセルの製法、コアセルベーンコン法) テトラクロルエチレン80部を10重重量上ラチン水溶
液150部中に分散させ、ゆるやかに攪拌し乳化させた
後、10重量%アラビアゴム水溶液150部を加え、更
に45℃の温水600部を加える。
Example 2 (Production method of microcapsules, core cell vanecon method) 80 parts of tetrachlorethylene was dispersed in 150 parts of a 10% by weight aqueous solution of latin, and after gently stirring and emulsifying, 150 parts of a 10% by weight aqueous gum arabic solution was dispersed. 1 part, and then 600 parts of 45°C warm water.

この溶液を40℃以上に保ちながら酢酸を滴下して+ 
I) II 4.1とした。そして、5℃まで冷却後、
グルタルアルデヒド25部を加えた。
Add acetic acid dropwise to this solution while keeping it at 40℃ or higher.
I) II 4.1. After cooling to 5℃,
25 parts of glutaraldehyde were added.

この状態で一晩放置後、カプセルをデカンテーションし
て、スラリーとし、バットに広げて風乾してテトラクロ
ルエチレン入りマイクロカプセル100部を得た。
After being left in this state overnight, the capsules were decanted to form a slurry, spread on a vat, and air-dried to obtain 100 parts of microcapsules containing tetrachlorethylene.

(消しゴムの製法) Geon21 150部 ジオクチルフタレート 150部 エポキシ化大豆油 6部 炭酸カルシウム 50部 上記成分を攪拌混合して、塩ビペーストを得た。(Eraser manufacturing method) Geon21 150 copies Dioctyl phthalate 150 parts Epoxidized soybean oil 6 parts Calcium carbonate 50 parts The above components were stirred and mixed to obtain a vinyl chloride paste.

この塩ビペースト656部に上述のマイクロカプセル1
00部を攪拌混合した後、110℃。
1 of the above-mentioned microcapsules was added to 656 parts of this PVC paste.
After stirring and mixing 00 parts, the mixture was heated to 110°C.

20分間、プレス成型して消しゴムを得た。An eraser was obtained by press molding for 20 minutes.

実施例5 (マイクロカプセルの製法、液中硬化法)同心二重オリ
フィス管の内側にキシレン、外側にアルギン酸ナトリウ
ム06重量%、ポリビニルアルコール12重量%、グリ
セリン12重量%、水75.4重量%よりなる液を供給
して。
Example 5 (Production method of microcapsules, in-liquid curing method) Concentric double orifice tube with xylene on the inside, 06% by weight of sodium alginate on the outside, 12% by weight of polyvinyl alcohol, 12% by weight of glycerin, and 75.4% by weight of water. supply the liquid.

射出して20重量%塩化カルシウム水溶液中に投入し、
キシレン入りのマイクロカプセルを得た。
Injected and poured into a 20% by weight calcium chloride aqueous solution,
Microcapsules containing xylene were obtained.

(消しゴムの製法) 実施例2で使用した塩ビペースト356部に上述したマ
イクロカプセル100部を加え。
(Production method of eraser) 100 parts of the above-mentioned microcapsules were added to 356 parts of the vinyl chloride paste used in Example 2.

攪拌混合した後、110℃、20分間、プレス成型して
消しゴムを得た。
After stirring and mixing, the mixture was press-molded at 110° C. for 20 minutes to obtain an eraser.

実施例4 (溶剤吸着多孔性粉体、無機物) 活性白土100部を高速攪拌し、攪拌中にイソホロン5
0部を滴下して、イソホロ/を吸着させた活性白土粉体
を得た。
Example 4 (Solvent-adsorbing porous powder, inorganic material) 100 parts of activated clay was stirred at high speed, and 5 parts of isophorone was added during stirring.
0 part was added dropwise to obtain activated clay powder adsorbed with isophoro/.

(消しゴムの製法) 実hfM例1中に使用した塩ビペースト313部に上述
のイソホロンを吸着させた活性白土粉体150部を攪拌
混合した後、110℃。
(Production method of eraser) 150 parts of the above-mentioned activated clay powder adsorbed with isophorone was stirred and mixed with 313 parts of the vinyl chloride paste used in Example 1 of the actual hfM, and the mixture was heated at 110°C.

20分間、プレス成型して消しゴムを得た。An eraser was obtained by press molding for 20 minutes.

実施例5 (溶剤吸着多孔性粉体、有機物) アビセル’l’Q−101(無化成■製、結晶セルロー
ス)100部を高速攪拌し、攪拌中に安息香酸エチル5
0部を滴下して、安息香酸エチルを吸着した結晶セルロ
ース粉体を得た。
Example 5 (Solvent-adsorbing porous powder, organic substance) 100 parts of Avicel'l'Q-101 (non-chemical, crystalline cellulose) was stirred at high speed, and during stirring 50 parts of ethyl benzoate was added.
0 part was added dropwise to obtain crystalline cellulose powder adsorbing ethyl benzoate.

(消しゴムの製l去) 実施例2に使用した塩ビペースト356部に」二連した
安息香酸エチルを吸着した結晶セルロース粉体150部
を加え、攪拌混合した後、110℃、20分間、プンス
成型して消しゴムを得だ。
(Production of eraser) To 356 parts of the PVC paste used in Example 2, 150 parts of crystalline cellulose powder adsorbed with double ethyl benzoate was added, stirred and mixed, and then molded at 110°C for 20 minutes. and got an eraser.

上述で得られた実施例1〜5の消しゴムで。With the erasers of Examples 1 to 5 obtained above.

トレーンングペーパーおよび製図用フィルムに静電複写
法で形成した画像を10回擦過したところ画像は容易に
消去修正できた1、 又、これらの修正跡に汚れはみられなかった。
When images formed by electrostatic copying on training paper and drafting film were rubbed 10 times, the images could be easily erased and corrected1, and no stains were observed in these correction marks.

以上のように9本発明の静電複写画像修正用消しゴムは
、優れた消去性を示し、又、修正跡の汚れも少ないもの
である。
As described above, the eraser for correcting electrostatic copying images of the present invention exhibits excellent erasability and leaves less stain after correction.

特許出願人 べんてる株式会社 手続上口IJEでテ(自発) 昭和59年12月夕日 特許庁長官 志 賀 学 殿 1、本件の表示 昭和58年特Iii′ll′!t5208862号2、
発IJIの名称 静電複写画像修正用消しゴム 3、補正をする者 本件との関係 特許出願人 チ、つオウフ 二本ノバノ コrミツ、つ〒103 住
 所 東京都中央区日本橋小絹町7番2号IjJ#1l
IFJの発明の詳細な説IIの欄6、補正あ内容 以上。
Patent Applicant: Bentel Co., Ltd. Proceeding at the Upper Exit IJE (Voluntary) Sunset, December 1980 Manabu Shiga, Commissioner of the Patent Office 1, Indication of this case 1982 Special Iii'll'! t5208862 No. 2,
Name of IJI: Eraser 3 for electrostatic photocopy image correction.Relationship to the case: Patent applicant: 103 Address: 7, Nihonbashi Kokinumachi, Chuo-ku, Tokyo No. 2 IjJ#1l
Column 6 of IFJ's Detailed Description of the Invention II, amended content and above.

Claims (1)

【特許請求の範囲】 1)下記条件を有する沸点120℃以上の溶剤を消しゴ
ム中に含有せしめた静電複写画像修正用消しゴム。 く条件〕〉 水素結合力が弱の時 溶解性ノ(ラメ−クー(S)が7
、0〜11.1 (cab/cm’)−’水素結合力が
中の時 溶解性ノ(ラメ−ター(S)が7、4〜14.
7 (cal /d )22)前記溶剤を芯物質とした
マイクロカフ”セルを消しゴム中に含有せしめたことを
特徴とする特許請求の範囲第1項記載の静電複写画像修
正用消しゴム。 5 ) tjfl記溶剤全溶剤させた多孔性粉体を消し
コ゛ム中に含有せしめたことを特徴とする特許請求の範
囲第1及び第2項記載の静電複写画像修正用消しゴム。
[Scope of Claims] 1) An eraser for correcting electrostatically copied images, which contains a solvent having a boiling point of 120° C. or higher and having the following conditions. Conditions]> When the hydrogen bonding force is weak, the solubility (Lamécou (S) is 7)
, 0 to 11.1 (cab/cm') - When the hydrogen bond strength is medium, the solubility parameter (S) is 7, 4 to 14.
7 (cal/d)22) The eraser for electrostatic copying image correction according to claim 1, characterized in that the eraser contains microcuff cells containing the solvent as a core material.5) An eraser for correcting electrostatic copying images according to claims 1 and 2, characterized in that the eraser contains a porous powder completely dissolved in a solvent.
JP20886283A 1983-11-07 1983-11-07 Eraser for correcting electrostatic copying picture Granted JPS60101098A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20886283A JPS60101098A (en) 1983-11-07 1983-11-07 Eraser for correcting electrostatic copying picture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20886283A JPS60101098A (en) 1983-11-07 1983-11-07 Eraser for correcting electrostatic copying picture

Publications (2)

Publication Number Publication Date
JPS60101098A true JPS60101098A (en) 1985-06-05
JPH0225800B2 JPH0225800B2 (en) 1990-06-05

Family

ID=16563346

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20886283A Granted JPS60101098A (en) 1983-11-07 1983-11-07 Eraser for correcting electrostatic copying picture

Country Status (1)

Country Link
JP (1) JPS60101098A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01262198A (en) * 1988-04-12 1989-10-19 Tombow Pencil Co Ltd Plastic erasing composition

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54106325A (en) * 1978-02-08 1979-08-21 Pentel Kk Rubber eraser
JPS54135033A (en) * 1978-04-11 1979-10-19 Pentel Kk Eraser and making method thereof
JPS54156734A (en) * 1978-05-29 1979-12-11 Pentel Kk Eraser and making method thereof
JPS5530982A (en) * 1978-08-29 1980-03-05 Pentel Kk Eraser for pressureesensitive copying paper

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54106325A (en) * 1978-02-08 1979-08-21 Pentel Kk Rubber eraser
JPS54135033A (en) * 1978-04-11 1979-10-19 Pentel Kk Eraser and making method thereof
JPS54156734A (en) * 1978-05-29 1979-12-11 Pentel Kk Eraser and making method thereof
JPS5530982A (en) * 1978-08-29 1980-03-05 Pentel Kk Eraser for pressureesensitive copying paper

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01262198A (en) * 1988-04-12 1989-10-19 Tombow Pencil Co Ltd Plastic erasing composition

Also Published As

Publication number Publication date
JPH0225800B2 (en) 1990-06-05

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