JPS5849761A - Correction fluid - Google Patents

Correction fluid

Info

Publication number
JPS5849761A
JPS5849761A JP56145214A JP14521481A JPS5849761A JP S5849761 A JPS5849761 A JP S5849761A JP 56145214 A JP56145214 A JP 56145214A JP 14521481 A JP14521481 A JP 14521481A JP S5849761 A JPS5849761 A JP S5849761A
Authority
JP
Japan
Prior art keywords
resin
correction fluid
parts
organic solvent
white pigment
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
JP56145214A
Other languages
Japanese (ja)
Other versions
JPS644548B2 (en
Inventor
Eiichi Okabe
鋭一 岡部
Yasuhiro Takahashi
安宏 高橋
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 JP56145214A priority Critical patent/JPS5849761A/en
Publication of JPS5849761A publication Critical patent/JPS5849761A/en
Publication of JPS644548B2 publication Critical patent/JPS644548B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D10/00Correcting fluids, e.g. fluid media for correction of typographical errors by coating

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)

Abstract

PURPOSE:To obtain a correction fluid giving a coating film rewritable with a water-based ink leaving easily dryable written mark, by using a specific imidazoline derivative in combination with a white pigment, an organic solvent and a resin. CONSTITUTION:The objective correction fluid is composed of (A) a white pigment such as titanium oxide, (B) an organic solvent (preferably having a boiling point of 70-150 deg.C, e.g. toluene, trichloroethane, methyl ethyl ketone, etc.), (C) a resin soluble in the solvent (B) (e.g. acrylic resin, alkyd resin, vinyl resin, polyester, etc.) and (D) an imidazoline derivative of formula (R1 is alkyl, phenyl, or fatty acid residue; R2 is H or alkyl) (preferably a compound obtained by adding ethylene oxide and ethylene carbonate to the 1-position of 2- and/or 4-substituted imidazoline). The preferable weight ratios of A:B:C:D are (20-50):(30-60):(5-20): (0.1-3).

Description

【発明の詳細な説明】 本発明は、修正液に関し、更に詳しくは、修正個所の塗
膜を水性インキ使用の万年筆、サインペンなどにより再
筆記可能にするとともに再暗記した筆跡の乾燥性に優れ
几塗膜が得られるようになした修正液に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a correction fluid, and more specifically, the present invention relates to a correction fluid that enables rewriting of a coating film at a correction point with a fountain pen, felt-tip pen, etc. using water-based ink, and has excellent drying properties for rememorized handwriting. This invention relates to a correction fluid that allows a coating film to be obtained.

従来、油性の修i液に(より修正した個所は。Conventionally, oil-based repair solution (for areas that have been repaired).

疎水性を呈しているため、水性インキ使用の万年筆、サ
インペンなどにより再筆記した場合。
Because it is hydrophobic, if it is rewritten with a fountain pen, felt-tip pen, etc. that uses water-based ink.

水性インキがはじかれてしまい再筆記が困難あ町るいは
再筆記できLとしても筆跡の乾燥が悪いという問題を有
していた。
There was a problem that the water-based ink was repelled and it was difficult to write again, and even if it was possible to write again, the handwriting dried poorly.

本発明者らは、上述せる問題を解決すべく。The present inventors aimed to solve the above-mentioned problems.

油性の修正液に添加する物質について種々検討の結果、
遂に本発明を完成したものであって。
As a result of various studies on substances to be added to oil-based correction fluid,
This invention has finally been completed.

本発明は、白色顔料と、有機溶剤と、有機溶剤に可溶な
樹脂と、下記一般式で示すイミダシリン誘導体とからな
る修正液を要旨とするものである。
The gist of the present invention is a correction fluid comprising a white pigment, an organic solvent, a resin soluble in the organic solvent, and an imidacillin derivative represented by the following general formula.

本発明に於て、一般式で示すイミダシリン誘導体を使用
することによって、修非個所の塗膜面に水性イン4で筆
記した場合、何故、水性インキをはじくことなく再筆記
可能であって、再筆記した筆跡の乾燥が良好になるのか
は定がでないが、イミダシリン誘導体の2位及び/又は
4位の置換基が親油性基として働き、1位のヒドロキシ
エチル化の水酸基が親水性基として働くため、イミダシ
リン誘導体は、非イオン性の界面活性剤と同様の機能を
有しており、この機能と前述の親水性の水酸基の機能と
により、塗膜へのインキののりを良好にし、インキのは
じき防止、更にはインキの塗膜への浸透を良好にし筆跡
の乾燥が良好になるものと思われる。又。
In the present invention, by using the imidacillin derivative represented by the general formula, when writing with water-based ink 4 on the paint surface of the repaired area, why can it be rewritten without repelling the water-based ink? Although it is not certain whether the handwriting will dry well, the substituent at the 2- and/or 4-position of the imidacillin derivative acts as a lipophilic group, and the hydroxyethylated hydroxyl group at the 1-position acts as a hydrophilic group. Therefore, imidacillin derivatives have a function similar to that of nonionic surfactants, and this function and the function of the hydrophilic hydroxyl group mentioned above improve the adhesion of the ink to the coating film and improve the adhesion of the ink. It is thought that it prevents repelling and also improves the penetration of the ink into the coating film, thereby improving the drying of handwriting. or.

本発明に於けるイミダゾリ/誘導体は、前述のように非
イオン界面活性剤と同様の機能を有しており、顔料の分
散性向上、沈降防上にも寄与しているものと思われる。
The imidazolyte/derivative in the present invention has the same function as a nonionic surfactant as described above, and is thought to contribute to improving the dispersibility of pigments and preventing sedimentation.

以下1本発明の組成について説明する。The composition of the present invention will be explained below.

白色顔料は、筆跡を隠蔽するために使用するものであっ
て、ルチル型、アナターゼ型などの各種の酸化チタンが
使用でき、市販のものとしてFi、 タイト−/5R−
1,同R−、650.同R−3L、同R−310,同A
−110.同人−150.同R−5N (以上、堺化学
工業■製)タイベークR−580.同R−550,同R
−950、同A−1−00.同A−220(以上。
The white pigment is used to hide handwriting, and various titanium oxides such as rutile type and anatase type can be used, and commercially available ones include Fi, Tite-/5R-
1, R-, 650. Same R-3L, Same R-310, Same A
-110. Doujin-150. Same R-5N (manufactured by Sakai Chemical Industry Co., Ltd.) Tybake R-580. Same R-550, Same R
-950, same A-1-00. Same A-220 (and above).

石原産業■製)、クロノス〜KR−310,同KR−5
80.同KR−480.同KA−10゜同KA−20.
同KA−30(以上1 fl’7エ業■製)などが槙げ
られ、他の成分などを考慮すると、その使用量は修正液
全量に対して20〜50重IIチが好ましい。
Made by Ishihara Sangyo ■), Kronos ~ KR-310, KR-5
80. Same KR-480. Same KA-10゜ Same KA-20.
The same KA-30 (manufactured by 1 fl'7 Industrial Co., Ltd.) is used, and when other components are considered, the amount used is preferably 20 to 50 parts per total amount of correction fluid.

有機溶剤は、樹脂の溶解、粘度祠祭などに使用されるも
ので、トルエン、キシレン、n−ヘプタン、n−オクタ
ン、シクロヘキサン、メチルシクロヘキサンなどの炭化
水素系、1.1.1−トリクロルエタン、テトラクロル
エチレ7などのハロゲン炭化水素系、1.4−ジオキサ
7、  fi−ブチルエーテル、トリオキサ/などのt
−チル系、エチルメチルケト/、メチル−n −/’ 
0ピルケトンなどのケトン系、ギ酸プロピル、酢酸エチ
ルなどのエステル系など示あ゛9.修正した個所の塗膜
の乾燥時間を考慮すれば沸点が70℃〜1°50℃のも
のが好ましく、単独もしくは混合して使用可能であり、
その使用量は修正液全量に対して30〜60重量%が好
ましい。
Organic solvents are those used for dissolving resins, viscosity rituals, etc., and include hydrocarbons such as toluene, xylene, n-heptane, n-octane, cyclohexane, and methylcyclohexane, 1.1.1-trichloroethane, Halogenated hydrocarbons such as tetrachloroethyle7, 1,4-dioxa7, fi-butyl ether, trioxa/etc.
-thyl system, ethyl methyl keto/, methyl-n -/'
Ketones such as zero-pyl ketone, esters such as propyl formate, ethyl acetate, etc.9. Considering the drying time of the paint film in the corrected area, those with a boiling point of 70°C to 1°50°C are preferable, and can be used alone or in combination.
The amount used is preferably 30 to 60% by weight based on the total amount of correction fluid.

尚、n−へブタン、n−オクタンなどのパラフィン系炭
化水素−や、シクロヘキサン、メチルシクロヘキサンな
どのナフチ/系炭化水素を有機溶剤として使用すれば、
油性インキの筆跡をも修正・rることがでへるものであ
る。
In addition, if paraffinic hydrocarbons such as n-hebutane and n-octane and naphthyl hydrocarbons such as cyclohexane and methylcyclohexane are used as organic solvents,
It is also possible to correct and erase handwriting made with oil-based ink.

有機溶剤に11丁清々樹脂としては、−例を挙げると、
アクリル樹脂、アルキッド園脂、ビニル樹脂、ポリエス
テル樹脂などが、sv、単独もしくは混合して使用可能
であり2.その使用量は修正液全量に対して5〜20重
量%が好ましい。
For example, 11 types of resin can be used in organic solvents.
Acrylic resin, alkyd resin, vinyl resin, polyester resin, etc. can be used alone or in combination.2. The amount used is preferably 5 to 20% by weight based on the total amount of correction fluid.

本発明の骨子である一般式で示されるイミダシリン誘導
体は、2位及び/又は4位の置換イミダシリンの1位に
酸化エチレンあるいはエチレンカーボナートを付加する
か、エチレンクロールヒドリンで置換するかして、1−
ヒドロキシエチル化物とし穴ものであり、市販されてい
るものあるいは、前述のように合成したものであっても
よく、その使用量は修正液全量に対して、0.1重量%
以下では効果が少ないことがあり、3重量%以上ではこ
れ以上の効果が期待できないため、0.1〜5重量%が
好ましい。
The imidacillin derivative represented by the general formula, which is the gist of the present invention, can be obtained by adding ethylene oxide or ethylene carbonate to the 1st position of imidacillin substituted at the 2nd and/or 4th positions, or by substituting it with ethylene chlorohydrin. , 1-
It is a hydroxyethylated product, and may be a commercially available product or a product synthesized as described above, and the amount used is 0.1% by weight based on the total amount of correction fluid.
If it is less than 3% by weight, the effect may be small, and if it is more than 3% by weight, no further effect can be expected, so 0.1 to 5% by weight is preferable.

尚、上記せる成分の他に紙などの筆記面と色調を合わせ
る為に着色顔料を、隠蔽力を向上させる為にシリカ、炭
酸カルシウムなどの体質顔料を、顔料の分散安定性の為
に分散剤や沈降防上剤を、粘度調整の為に増粘剤を、塗
膜の硬さを調整する為に可塑剤を、塗布性能を良好にな
らしめる為にフロー向上剤やレベリング剤を適宜少量添
加することができる。
In addition to the above ingredients, coloring pigments are used to match the color tone with the writing surface such as paper, extender pigments such as silica and calcium carbonate are used to improve hiding power, and dispersants are used to stabilize the dispersion of pigments. Add a small amount of anti-sedimentation agent, thickener to adjust the viscosity, plasticizer to adjust the hardness of the coating film, flow improver or leveling agent to improve coating performance. can do.

本発明の修正液は、上記各成分をボールミル。The correction fluid of the present invention is prepared by ball milling each of the above components.

アトライター、サンドグライダ−などの攪拌分散機を使
用して分散混合することによって得られる。
It is obtained by dispersing and mixing using a stirring disperser such as an attritor or a sand glider.

このようにして得られた本発明の修正液で修正し次個所
の塗膜は、水性インキで再筆記できるとともに再筆記し
た筆跡の乾燥も良好なものである。
The thus obtained coating film corrected with the correction liquid of the present invention can be rewritten with water-based ink, and the rewritten handwriting dries well.

以下、実施例に従い1本発明を更に詳細に説明するが、
実施例中「部」とあるのは「重量部」を示す。
Hereinafter, the present invention will be explained in more detail according to Examples.
In the examples, "parts" indicate "parts by weight."

実施例 1 クロノスKR−380(白色顔料)     60部ダ
イヤナールBR105(三菱レイヨン■製、アクリル樹
脂)15部キシレン              Zf
1部イミダシリン誘導体           1部(
R1=ヤシ油脂肪酸残基、’R2=)Iであるイミダシ
リン誘導体、用研ファインケミカル″掬製) ミズカミルP−801(水沢化学■、微細シリカ)  
 2部上記各成分をボールミルにて24時間分散処理し
て修正液を得た。
Example 1 Kronos KR-380 (white pigment) 60 parts Dianal BR105 (manufactured by Mitsubishi Rayon, acrylic resin) 15 parts Xylene Zf
1 part imidacillin derivative 1 part (
R1=coconut oil fatty acid residue, 'R2=)I imidacillin derivative, manufactured by Yoken Fine Chemicals "Kiki") Mizukamil P-801 (Mizusawa Chemical ■, fine silica)
Two parts of each of the above components were dispersed in a ball mill for 24 hours to obtain a correction fluid.

実施例 2 クロノスKR−38060部 パ91 )”B−66(ローム&)・−ス社製。Example 2 Kronos KR-38060 part Pa91)"B-66 (manufactured by Rohm &).

アクリル樹脂)   12部 1、1.1−トリクロロニータン     110部イ
ミダシリン誘導体         1部(Rt = 
044)(j8.R産=Hである2、4位置換イミダシ
リン(C11ZL、四国化成工業■製)の1位をエチレ
ンクロールヒドリンにて置換したもの。) 2部 MA−400(三菱化成編製、カーボンブラック)0.
02部 ゛上記各成分をボールミルにて24時間分散処
理して修正液を得た。
Acrylic resin) 12 parts 1,1,1-trichlornitane 110 parts Imidacillin derivative 1 part (Rt =
044) (J8. R product = H, 2- and 4-substituted imidacillin (C11ZL, manufactured by Shikoku Kasei Kogyo ■) whose 1st position is substituted with ethylene chlorohydrin.) 2 parts MA-400 (manufactured by Mitsubishi Kasei Corporation) , carbon black) 0.
02 parts ゛The above components were dispersed in a ball mill for 24 hours to obtain a correction liquid.

実施例 5 クロノスKR−48060部 パラロイドB−67(ローム&)1−ス社製。Example 5 Kronos KR-48060 part Paraloid B-67 (manufactured by Rohm &) 1-S.

アクリル樹脂)12部 メチルシクロヘキサン        40部エチルシ
クロヘキサン        20部イミダシリン誘導
体         1部(R1=OMHB、R旦=O
H!である2、4位置換イミダシリン(2E・4M7.
L、 四国化成工業■製)の1位をエチレンクロールヒ
ドリンにて置換したもの。) ミズカミルP−8011,5部 DOA(大入化学■、可塑剤)     4部上記各成
分をボールミルにて24時間分散処理して修正液を得た
Acrylic resin) 12 parts Methylcyclohexane 40 parts Ethylcyclohexane 20 parts Imidacillin derivative 1 part (R1=OMHB, Rdan=O
H! Imidacillin substituted at the 2 and 4 positions (2E・4M7.
L, manufactured by Shikoku Kasei Kogyo ■) in which the 1st position is substituted with ethylene chlorohydrin. ) Mizukamil P-8011, 5 parts DOA (Oiri Kagaku ■, plasticizer) 4 parts Each of the above components was dispersed in a ball mill for 24 hours to obtain a correction fluid.

実施例 4 クロノスKR−38060部 ダイヤナールBR−105,15部 メチルシクロヘキサン         40部ペガゾ
ールLA(モーピル石油■、パラフィン系溶剤)   
20部イミダシリン誘導体(実施例1と同様なもの) 
    1部ミズカミルP−8011,5部 DOA                   S部ポ
リフローS(共栄社油脂■、フロー向上剤)0,2部上
記各成分をボールミルにて24時間分散処理して修正液
を得た。
Example 4 60 parts of Kronos KR-380 15 parts of Dyanaru BR-105 40 parts of methylcyclohexane Pegasol LA (Mopil Petroleum ■, paraffinic solvent)
20 parts imidacillin derivative (same as Example 1)
1 part Mizukamil P-8011, 5 parts DOA, S part Polyflow S (Kyoeisha Yushi ■, flow improver) 0.2 parts The above components were dispersed in a ball mill for 24 hours to obtain a correction fluid.

比較例1〜4 実施例1〜4のイミダシリン誘導体を除い友他は実施例
と同様にして修正液を得た。
Comparative Examples 1 to 4 Correction fluids were obtained in the same manner as in Examples except for the imidacillin derivatives of Examples 1 to 4.

実施例1〜4.比較例1〜4の修正液の隠蔽率。Examples 1-4. Hiding rate of correction fluids of Comparative Examples 1 to 4.

再筆記性、塗膜乾燥時間、指触乾燥時間の試験結果を表
−1に示す。−・ 昭和tア年//月j日 特許庁長官  若 杉和 夫 殿 1、 事件の表示 昭和56年特許願第145214号 Z 発明の名称 修   正   液 3、 補正をす゛る者 4、 補正命令の日付  自 発 明の詳細な説明の欄の記載を次の正誤表に特開昭58−
49761(4:) 従って補正する。
Table 1 shows the test results for rewriting properties, coating film drying time, and touch drying time. - Kazuo Wakasugi, Commissioner of the Japan Patent Office, July 1972, 1, Indication of the case, Patent Application No. 145214, filed in 1982, Amendment of the name of the invention, 3, Person making the amendment, 4, Order for amendment Date From: JP-A-58-1999, the description in the column of detailed description of the invention is written in the following errata.
49761 (4:) Correct accordingly.

Claims (1)

【特許請求の範囲】[Claims] 白色顔料と、有機溶剤と、有機溶剤′に可溶な樹脂と、
下記一般式で示すイミダシリン誘導体とからなる修正液
A white pigment, an organic solvent, a resin soluble in the organic solvent,
A correction liquid consisting of an imidacillin derivative represented by the general formula below.
JP56145214A 1981-09-14 1981-09-14 Correction fluid Granted JPS5849761A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56145214A JPS5849761A (en) 1981-09-14 1981-09-14 Correction fluid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56145214A JPS5849761A (en) 1981-09-14 1981-09-14 Correction fluid

Publications (2)

Publication Number Publication Date
JPS5849761A true JPS5849761A (en) 1983-03-24
JPS644548B2 JPS644548B2 (en) 1989-01-26

Family

ID=15380004

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56145214A Granted JPS5849761A (en) 1981-09-14 1981-09-14 Correction fluid

Country Status (1)

Country Link
JP (1) JPS5849761A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS606765A (en) * 1983-06-27 1985-01-14 Pentel Kk Retouching liquid
JPS608376A (en) * 1983-06-27 1985-01-17 Pentel Kk Eraser solution
JPH07166114A (en) * 1993-10-12 1995-06-27 Orient Chem Ind Ltd Correcting solution of coloring recording material
US5594045A (en) * 1992-06-03 1997-01-14 Alexiou; Michael Correction fluids
US5922400A (en) * 1997-01-09 1999-07-13 The Gillette Company Correction fluid
US5925693A (en) * 1994-07-08 1999-07-20 The Gillette Company Aqueous correction fluids

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS606765A (en) * 1983-06-27 1985-01-14 Pentel Kk Retouching liquid
JPS608376A (en) * 1983-06-27 1985-01-17 Pentel Kk Eraser solution
US5594045A (en) * 1992-06-03 1997-01-14 Alexiou; Michael Correction fluids
US5726221A (en) * 1992-06-03 1998-03-10 The Gillette Company Correction fluids
JPH07166114A (en) * 1993-10-12 1995-06-27 Orient Chem Ind Ltd Correcting solution of coloring recording material
US5925693A (en) * 1994-07-08 1999-07-20 The Gillette Company Aqueous correction fluids
US5922400A (en) * 1997-01-09 1999-07-13 The Gillette Company Correction fluid

Also Published As

Publication number Publication date
JPS644548B2 (en) 1989-01-26

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