JPH10338828A - Dot printing ink - Google Patents

Dot printing ink

Info

Publication number
JPH10338828A
JPH10338828A JP16816397A JP16816397A JPH10338828A JP H10338828 A JPH10338828 A JP H10338828A JP 16816397 A JP16816397 A JP 16816397A JP 16816397 A JP16816397 A JP 16816397A JP H10338828 A JPH10338828 A JP H10338828A
Authority
JP
Japan
Prior art keywords
ink
weight
fatty acids
fatty acid
carbon atoms
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
JP16816397A
Other languages
Japanese (ja)
Other versions
JP3794786B2 (en
Inventor
Haruhisa Tominaga
晴久 富永
Kenji Kamiya
謙二 上谷
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.)
Shachihata Inc
Original Assignee
Shachihata Inc
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 Shachihata Inc filed Critical Shachihata Inc
Priority to JP16816397A priority Critical patent/JP3794786B2/en
Publication of JPH10338828A publication Critical patent/JPH10338828A/en
Application granted granted Critical
Publication of JP3794786B2 publication Critical patent/JP3794786B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a dot printing ink which can give dots which do not undergo repulsion or blotting even when applied to a lens hard-coated with a film of a silicone, a fluoro resin or the like and can be perfectly and easily erased simply by wiping off with e.g. a cloth when become useless. SOLUTION: This ink comprises at least one solvent selected among esters of 14-20C saturated or unsaturated fatty acids or hydroxy fatty acids derived therefrom with 1-4C aliphatic alcohols and ethers of hydroxy fatty acids derived from 14-20C saturated or unsaturated fatty acids with 1-4C aliphatic alcohols, a colorant, and 0.3-0.7 wt.%, based on the total ink weight, fluorine-containing surfactant.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、ハードコートされ
た眼鏡レンズに用いる印点インキに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a printing ink for a hard-coated spectacle lens.

【0002】[0002]

【従来の技術】従来より、眼鏡レンズには視点を明確に
するために、メーカーの出荷時において、あらかじめ印
点を施すことが行なわれている。印点の際は、インキを
充填させた筆記具のようなマーカーや、多孔性ゴムにイ
ンキを含浸させた浸透印を用いるとインキをたびたび補
充することなく連続して印点できるので有用であり、実
開昭52−167306などが知られている。しかし、
近年シリコン系やフッ素系などの被膜でハードコートさ
れたレンズが開発され、このようなレンズに対して従来
の印点インキはハジキやニジミを生じるようになり、正
確な印点業務に支障を生じるようになった。また、印点
は販売時に跡が残らないよう完全に除去できることが求
められるが、従来のインキは完全に除去することが困難
であった。
2. Description of the Related Art Conventionally, in order to clarify the viewpoint, spectacle lenses have been marked in advance at the time of shipment from a manufacturer. In the case of a marking point, it is useful to use a marker such as a writing instrument filled with ink, or a penetration mark in which porous rubber is impregnated with ink, since it is possible to continuously mark without frequently refilling the ink, JP-A-52-167306 is known. But,
In recent years, lenses hard-coated with silicon-based or fluorine-based coatings have been developed, and conventional marking inks for such lenses will cause cissing and bleeding, which will hinder accurate marking work. It became so. Further, it is required that the mark points can be completely removed so that no trace is left at the time of sale, but it has been difficult to completely remove the conventional ink.

【0003】[0003]

【発明が解決しようとする課題】そこで、本発明者は、
シリコン系やフッ素系などの被膜でハードコートされた
レンズに対してもハジキやニジミを生じず、不要となっ
た時は布等で拭き取るだけで完全かつ容易に印点が除去
できる印点インキを発明した。
Therefore, the present inventor has proposed:
No spotting or bleeding occurs on lenses hard-coated with silicon-based or fluorine-based coatings. When not needed, simply remove the marking ink with a cloth or similar to remove the marking ink completely and easily. Invented.

【0004】[0004]

【課題を解決するための手段】炭素数14〜20の飽和
脂肪酸もしくは不飽和脂肪酸又はこれらから誘導される
ヒドロキシ脂肪酸と炭素数1〜4の脂肪族アルコールと
のエステル、及び、炭素数14〜20の飽和脂肪酸又は
不飽和脂肪酸から誘導されるヒドロキシ脂肪酸と炭素数
1〜4の脂肪族アルコールとのエーテルから選ばれる1
又は2以上の溶剤と、着色剤と、インキ全量に対して
0.3〜0.7重量%のフッ素系界面活性剤とからなる
印点インキ。
Means for Solving the Problems An ester of a saturated fatty acid or unsaturated fatty acid having 14 to 20 carbon atoms or a hydroxy fatty acid derived therefrom with an aliphatic alcohol having 1 to 4 carbon atoms, and 14 to 20 carbon atoms Selected from ethers of hydroxy fatty acids derived from saturated or unsaturated fatty acids of the formula (I) and aliphatic alcohols having 1 to 4 carbon atoms.
Alternatively, a dot ink comprising two or more solvents, a colorant, and 0.3 to 0.7% by weight of a fluorine-based surfactant based on the total amount of the ink.

【0005】以下、本発明を詳細に説明する。本発明で
は、炭素数14〜20の飽和脂肪酸もしくは不飽和脂肪
酸又はこれらから誘導されるヒドロキシ脂肪酸と炭素数
1〜4の脂肪族アルコールとのエステル、及び、炭素数
14〜20の飽和脂肪酸又は不飽和脂肪酸から誘導され
るヒドロキシ脂肪酸と炭素数1〜4の脂肪族アルコール
とのエーテルから選ばれる1又は2以上の溶剤を用いる
ことができる。前記の炭素数14〜20の飽和脂肪酸も
しくは不飽和脂肪酸又はこれらから誘導されるヒドロキ
シ脂肪酸と炭素数1〜4の脂肪族アルコールとのエステ
ルとは、具体的には、パルミチン酸、ステアリン酸等の
飽和脂肪酸、もしくは、エレオステアリン酸、オレイン
酸、リノール酸、リノレン酸等の不飽和脂肪酸、又は、
前記飽和脂肪酸又は前記不飽和脂肪酸から誘導されるヒ
ドロキシステアリン酸、リシノール酸等のヒドロキシ脂
肪酸から任意に選定される脂肪酸と、メタノール、エタ
ノール、n−プロパノール、イソプロパノール、n−ブ
タノール、イソブタノール、sec−ブタノール、te
rt−ブタノールから任意に選定される脂肪族アルコー
ルとのエステルをいい、例えば、ステアリン酸メチル、
オレイン酸エチル、リノール酸n−プロピル、リシノー
ル酸n−ブチル等をあげることができる。前記の炭素数
14〜20の飽和脂肪酸又は不飽和脂肪酸から誘導され
るヒドロキシ脂肪酸と炭素数1〜4の脂肪族アルコール
とのエーテルとは、具体的には、ヒドロキシステアリン
酸、リシノール酸等から任意に選定されるヒドロキシ脂
肪酸と、メタノール、エタノール、n−プロパノール、
イソプロパノール、n−ブタノール、イソブタノール、
sec−ブタノール、tert−ブタノールから任意に
選定される脂肪族アルコールとのエーテルをいい、例え
ば、ヒドロキシステアリン酸メチルエーテル、リシノー
ル酸エチルエーテル、ヒドロキシステアリン酸n−プロ
ピルエーテル、リシノール酸n−ブチルエーテル等をあ
げることができる。本発明では、前記エステル及び前記
エーテルからなる溶剤群から任意に選ばれる1又は2以
上の溶剤を用いることができる。これらの溶剤は、不乾
性溶剤なので、インキのドライアップを防止し、インキ
が眼鏡レンズに固着することを防止する。また、インキ
を乾燥固化させないので、眼鏡レンズからのインキの拭
き取りを容易にする。本発明において、前記溶剤はイン
キ全量に対して40〜99重量%使用することができ
が、好ましい範囲は、60〜95重量%である。
Hereinafter, the present invention will be described in detail. In the present invention, an ester of a saturated fatty acid or unsaturated fatty acid having 14 to 20 carbon atoms or a hydroxy fatty acid derived therefrom with an aliphatic alcohol having 1 to 4 carbon atoms, and a saturated fatty acid or unsaturated fatty acid having 14 to 20 carbon atoms. One or more solvents selected from ethers of hydroxy fatty acids derived from saturated fatty acids and aliphatic alcohols having 1 to 4 carbon atoms can be used. The above-mentioned ester of a saturated fatty acid or unsaturated fatty acid having 14 to 20 carbon atoms or a hydroxy fatty acid derived therefrom and an aliphatic alcohol having 1 to 4 carbon atoms is specifically exemplified by palmitic acid, stearic acid and the like. Saturated fatty acids, or unsaturated fatty acids such as eleostearic acid, oleic acid, linoleic acid, linolenic acid, or
A fatty acid arbitrarily selected from hydroxy fatty acids such as hydroxystearic acid and ricinoleic acid derived from the saturated fatty acid or the unsaturated fatty acid, and methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec- Butanol, te
refers to esters with aliphatic alcohols arbitrarily selected from rt-butanol, for example, methyl stearate,
Examples thereof include ethyl oleate, n-propyl linoleate, and n-butyl ricinoleate. The ether of a hydroxy fatty acid derived from a saturated fatty acid having 14 to 20 carbon atoms or an unsaturated fatty acid and an aliphatic alcohol having 1 to 4 carbon atoms may be, for example, any of hydroxy stearic acid and ricinoleic acid. A hydroxy fatty acid selected for methanol, ethanol, n-propanol,
Isopropanol, n-butanol, isobutanol,
sec-butanol or tert-butanol, which means an ether with an aliphatic alcohol arbitrarily selected from, for example, hydroxystearic acid methyl ether, ricinoleic acid ethyl ether, hydroxystearic acid n-propyl ether, ricinoleic acid n-butyl ether, etc. I can give it. In the present invention, one or two or more solvents arbitrarily selected from a solvent group consisting of the ester and the ether can be used. Since these solvents are non-drying solvents, they prevent the ink from drying up and prevent the ink from sticking to the spectacle lens. Further, since the ink is not dried and solidified, it is easy to wipe off the ink from the spectacle lens. In the present invention, the solvent can be used in an amount of 40 to 99% by weight based on the total amount of the ink, but a preferable range is 60 to 95% by weight.

【0006】着色剤としては、公知の顔料及び油溶性染
料の中から任意の1又は2以上を選択して使用すること
ができる。顔料としては、特に制限されることなく従来
公知の有機顔料及び無機顔料を使用することができ、例
えば、アゾ系、フタロシアニン系、キナクリドン系、ア
ントラキノン系、ジオキサジン系、インジゴ・チオイン
ジゴ系、ベリノン・ベリレン系、イソインドレノン系、
アゾメチレンアゾ系などの有機顔料や、カーボンブラッ
ク、マイカ、チタン白、パール顔料、酸化鉄・アルミニ
ウム粉・真鍮等金属顔料などの無機顔料を用いることが
できる。これらの顔料は、ロジン、ロジンエステル、ロ
ジン誘導体、フェノール樹脂、エチルセルロース、ニト
ロセルロース、ケトン樹脂、塩化ビニル、酢酸ビニル、
塩化ビニル−酢酸ビニル共重合体、ポリアクリル酸、ポ
リメタクリル酸、スチレン−アクリル酸共重合体、ポリ
ビニルブチラールなどの顔料分散剤や、他の公知の顔料
分散剤などに練り込んで加工顔料としておくと溶剤と混
合する際に容易に分散するので便利である。また、既に
分散剤中に顔料を練り込んである市販の加工顔料を用い
ても良好な結果が得られる。染料としては、特に制限さ
れることなく従来公知の油溶性染料を使用することがで
き、例えば、モノアゾ系、ジスアゾ系、金属錯塩型モノ
アゾ系、アントラキノン系、フタロシアニン系、トリア
リルメタン系などを用いることができる。本発明ではい
わゆるインキ分かれが生じにくいので、色合いを勘案し
ながら前記顔料及び前記油溶性染料の着色剤群から選ば
れる1又は2以上の着色剤を任意に選定して使用するこ
とができる。本発明において、前記着色剤はインキ全量
に対して0.5〜20重量%使用することができる。
As the colorant, any one or more of known pigments and oil-soluble dyes can be selected and used. As the pigment, conventionally known organic pigments and inorganic pigments can be used without particular limitation. System, isoindolenone system,
Organic pigments such as azomethylene azo, and inorganic pigments such as carbon black, mica, titanium white, pearl pigments, and metal pigments such as iron oxide, aluminum powder, and brass can be used. These pigments are rosin, rosin ester, rosin derivative, phenolic resin, ethyl cellulose, nitrocellulose, ketone resin, vinyl chloride, vinyl acetate,
Kneaded into a pigment dispersant such as vinyl chloride-vinyl acetate copolymer, polyacrylic acid, polymethacrylic acid, styrene-acrylic acid copolymer, polyvinyl butyral, and other known pigment dispersants to prepare a processed pigment. And is easily dispersed when mixed with a solvent. Good results can also be obtained by using a commercially available processed pigment in which the pigment is already kneaded in the dispersant. As the dye, conventionally known oil-soluble dyes can be used without any particular limitation.For example, monoazo, disazo, metal complex salt type monoazo, anthraquinone, phthalocyanine, triallylmethane and the like are used. be able to. In the present invention, since so-called ink separation is unlikely to occur, one or two or more colorants selected from the colorant group of the pigment and the oil-soluble dye can be arbitrarily selected and used while taking into account the hue. In the present invention, the colorant may be used in an amount of 0.5 to 20% by weight based on the total amount of the ink.

【0007】他に本発明では、フッ素系界面活性剤が必
須構成要素であり、例えば、フロラードFC−126、
FC−176、FC−430(以上、住友スリーエム社
製フッ素系界面活性剤)などが好ましく用いられる。当
該フッ素系界面活性剤は、インキ全量に対して0.3〜
0.7重量%使用させることができ、フッ素系界面活性
剤を配合した後の本発明インキの表面張力を20m・N
/m以下にすることが好ましい。ハードコートが施され
た眼鏡レンズにおいて、前記フッ素系界面活性剤が0.
3重量%より少ない場合はインキのハジキが生じてしま
い、0.7重量%より多い場合はインキのニジミが生じ
てしまうので好ましくない。また、フッ素系界面活性剤
を配合した後の本発明インキの表面張力が20m・N/
mより高いとインキのハジキが生じてしまうので好まし
くない。
In the present invention, a fluorine-containing surfactant is an essential component, and examples thereof include Florad FC-126,
FC-176 and FC-430 (the above are fluorine-based surfactants manufactured by Sumitomo 3M) are preferably used. The fluorine-based surfactant is 0.3 to the total amount of the ink.
0.7% by weight, and the surface tension of the ink of the present invention after blending a fluorine-based surfactant is 20 m · N
/ M or less. In a spectacle lens provided with a hard coat, the fluorine-based surfactant may be added in an amount of 0.1%.
When the amount is less than 3% by weight, repelling of the ink occurs, and when the amount is more than 0.7% by weight, bleeding of the ink occurs, which is not preferable. Further, the surface tension of the ink of the present invention after blending a fluorine-based surfactant is 20 m · N /
If it is higher than m, repelling of the ink occurs, which is not preferable.

【0008】本発明には他に、ジブチルヒドロキシトル
エン等の酸化防止剤や、チアベンダゾール等の防腐・防
かび剤、ロジン、ロジンエステル、ロジン誘導体、フェ
ノール樹脂、エチルセルロース、ニトロセルロース、ケ
トン樹脂、塩化ビニル、酢酸ビニル、塩化ビニル−酢酸
ビニル共重合体、ポリアクリル酸、ポリメタクリル酸、
スチレン−アクリル酸共重合体、ポリビニルブチラール
等の顔料分散剤などを任意に配合することができる。
The present invention also includes an antioxidant such as dibutylhydroxytoluene, an antiseptic and fungicide such as thiabendazole, rosin, rosin ester, rosin derivative, phenolic resin, ethylcellulose, nitrocellulose, ketone resin, vinyl chloride. , Vinyl acetate, vinyl chloride-vinyl acetate copolymer, polyacrylic acid, polymethacrylic acid,
A pigment dispersant such as a styrene-acrylic acid copolymer and polyvinyl butyral can be arbitrarily compounded.

【0009】以下、本発明を実施例をもって説明する
が、もちろん実施例に拘泥されるものでない。
Hereinafter, the present invention will be described with reference to examples, but it is needless to say that the present invention is not limited to the examples.

【0010】[0010]

【実施例1】 リシノール酸メチル 90重量% カーボンブラック 6重量% フロラードFC−430 0.4重量% (住友スリーエム社製フッ素系界面活性剤) ロジンエステル 3重量% ジブチルヒドロキシトルエン 0.6重量% 上記のカーボンブラックとロジンエステルを三本ロール
に投入し混合した後、これをプロペラ攪拌機にて残りの
物質と混合して黒色インキを得た。
Example 1 Methyl ricinoleate 90% by weight Carbon black 6% by weight Florad FC-430 0.4% by weight (fluorinated surfactant manufactured by Sumitomo 3M Limited) Rosin ester 3% by weight Dibutylhydroxytoluene 0.6% by weight The carbon black and the rosin ester were put into a three-roll mill and mixed, and then mixed with the remaining substances using a propeller stirrer to obtain a black ink.

【0011】[0011]

【実施例2】 リノール酸n−ブチル 95重量% ニグロシン 4重量% フロラードFC−430 0.5重量% (住友スリーエム社製フッ素系界面活性剤) ジブチルヒドロキシトルエン 0.5重量% 上記の物質をプロペラ攪拌機にて混合して黒色インキを
得た。
Example 2 95% by weight of n-butyl linoleate 4% by weight of nigrosine 0.5% by weight of Florade FC-430 (Fluorine surfactant manufactured by Sumitomo 3M) 0.5% by weight of dibutylhydroxytoluene The mixture was mixed with a stirrer to obtain a black ink.

【0012】[0012]

【実施例3】 ステアリン酸エチル 40重量% リシノール酸イソプロピルエーテル 40重量% カーボンブラック 10重量% フロラードFC−430 0.6重量% (住友スリーエム社製フッ素系界面活性剤) ニトロセルロース 9重量% ジブチルヒドロキシトルエン 0.4重量% 上記のカーボンブラックとニトロセルロースを三本ロー
ルに投入し混合した後、これをプロペラ攪拌機にて残り
の物質と混合して黒色インキを得た。
Example 3 Ethyl stearate 40% by weight Ricinoleic acid isopropyl ether 40% by weight Carbon black 10% by weight Florad FC-430 0.6% by weight (fluorinated surfactant manufactured by Sumitomo 3M Limited) Nitrocellulose 9% by weight Dibutylhydroxyl Toluene 0.4% by weight The above-mentioned carbon black and nitrocellulose were put into a three-roll mill and mixed, and then mixed with the remaining substance using a propeller stirrer to obtain a black ink.

【0013】[0013]

【比較例1】 リシノール酸メチル 90.5重量% カーボンブラック 6重量% ロジンエステル 3重量% ジブチルヒドロキシトルエン 0.5重量% 実施例1からフロラードFC−430を除いて黒色イン
キを作成した。
COMPARATIVE EXAMPLE 1 Methyl ricinoleate 90.5% by weight Carbon black 6% by weight Rosin ester 3% by weight Dibutylhydroxytoluene 0.5% by weight A black ink was prepared from Example 1 except that Florade FC-430 was omitted.

【0014】[0014]

【比較例2】 リシノール酸メチル 89.5重量% カーボンブラック 6重量% フロラードFC−430 1重量% (住友スリーエム社製フッ素系界面活性剤) ロジンエステル 3重量% ジブチルヒドロキシトルエン 0.5重量% 実施例1のフロラードFC−430を1重量%として黒
色インキを作成した。
Comparative Example 2 Methyl ricinoleate 89.5% by weight Carbon black 6% by weight Florad FC-430 1% by weight (fluorinated surfactant manufactured by Sumitomo 3M) Rosin ester 3% by weight Dibutylhydroxytoluene 0.5% by weight A black ink was prepared using 1% by weight of Florard FC-430 of Example 1.

【0015】以下、実施例1〜3、及び、比較例1〜2
の試験結果を表1に示す。試験は、連続気泡を有する多
孔性ゴムに上記各インキを含浸させたものを用いて印点
した。対象物は、シリコン系ハードコート被膜を施した
眼鏡レンズを使用した。
Hereinafter, Examples 1 to 3 and Comparative Examples 1 and 2
Table 1 shows the test results. The test was performed using a porous rubber having open cells impregnated with each of the above inks, and the test was marked. As an object, a spectacle lens provided with a silicon-based hard coat film was used.

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【効果】本発明の印点インキは、ハードコート被膜を施
した眼鏡レンズに印点したとき、ハジキもニジミも生じ
ず、かつ、完全にインキを拭き取り除去できる効果を有
するものである。
The marking ink according to the present invention has the effect of preventing cissing or bleeding when marking a spectacle lens provided with a hard coat film, and having the effect of completely wiping and removing the ink.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 炭素数14〜20の飽和脂肪酸もしくは
不飽和脂肪酸又はこれらから誘導されるヒドロキシ脂肪
酸と炭素数1〜4の脂肪族アルコールとのエステル、及
び、炭素数14〜20の飽和脂肪酸又は不飽和脂肪酸か
ら誘導されるヒドロキシ脂肪酸と炭素数1〜4の脂肪族
アルコールとのエーテルから選ばれる1又は2以上の溶
剤と、着色剤と、インキ全量に対して0.3〜0.7重
量%のフッ素系界面活性剤とからなる印点インキ。
1. An ester of a saturated fatty acid having 14 to 20 carbon atoms or an unsaturated fatty acid or a hydroxy fatty acid derived therefrom with an aliphatic alcohol having 1 to 4 carbon atoms, and a saturated fatty acid having 14 to 20 carbon atoms or One or two or more solvents selected from ethers of hydroxy fatty acids derived from unsaturated fatty acids and aliphatic alcohols having 1 to 4 carbon atoms, a colorant, and 0.3 to 0.7 wt. % Of a fluorine-based surfactant.
JP16816397A 1997-06-09 1997-06-09 Marking ink Expired - Fee Related JP3794786B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16816397A JP3794786B2 (en) 1997-06-09 1997-06-09 Marking ink

Applications Claiming Priority (1)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7169257B2 (en) 2003-11-12 2007-01-30 Kemira Chemicals, Inc. Method of deinking waste paper using a reduced alkali system
JP2010065172A (en) * 2008-09-12 2010-03-25 Shachihata Inc Dot printing ink
JP2010065074A (en) * 2008-09-08 2010-03-25 Shachihata Inc Oily ink for permeating seal

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7169257B2 (en) 2003-11-12 2007-01-30 Kemira Chemicals, Inc. Method of deinking waste paper using a reduced alkali system
JP2010065074A (en) * 2008-09-08 2010-03-25 Shachihata Inc Oily ink for permeating seal
JP2010065172A (en) * 2008-09-12 2010-03-25 Shachihata Inc Dot printing ink

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