JP3341065B2 - Ink composition for marking pen - Google Patents
Ink composition for marking penInfo
- Publication number
- JP3341065B2 JP3341065B2 JP31270494A JP31270494A JP3341065B2 JP 3341065 B2 JP3341065 B2 JP 3341065B2 JP 31270494 A JP31270494 A JP 31270494A JP 31270494 A JP31270494 A JP 31270494A JP 3341065 B2 JP3341065 B2 JP 3341065B2
- Authority
- JP
- Japan
- Prior art keywords
- ink composition
- ink
- melting point
- solvent
- resin
- 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 - Fee Related
Links
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明はマーキングペン用インキ
組成物に関し、詳細にはマーキングペンがキャップを外
され、ペン先が大気に露出された状態で長時間放置され
た後でも即座にマーキング可能な性能(以下、耐キャッ
プオフ性と称す)を備えたマーキングペン用インキ組成
物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an ink composition for a marking pen, and more particularly to a marking pen whose cap is removed and which can be immediately marked even after being left for a long time with the pen tip exposed to the atmosphere. The present invention relates to an ink composition for a marking pen having excellent performance (hereinafter referred to as cap-off resistance).
【0002】[0002]
【従来の技術】この種のマーキングペン用インキについ
ては、耐キャップオフ性を付与するための添加剤として
ポリグリセリンエステルを添加したインキ組成物(特公
昭62−34352号、特公平1−53707号及び特
公平3−49947号等)及び蔗糖エステルを添加した
インキ組成物(特公平1−49391号)等が提案され
ている。2. Description of the Related Art An ink composition containing a polyglycerin ester as an additive for imparting cap-off resistance is disclosed in JP-B-62-34352 and JP-B-1-53707. And Japanese Patent Publication No. 3-49947) and an ink composition to which a sucrose ester is added (Japanese Patent Publication No. 1-49391).
【0003】[0003]
【発明が解決しようとする課題】前記の従来技術による
マーキングペン用インキ組成物は、実用上の耐キャップ
オフ性を得るために前記添加剤の相当量の添加を必要と
し、それによりインキの対象物への密着性の低下が避け
られず、密着性が要求されない筆記板用マーキングペン
への適用に限られていた。The above ink compositions for marking pens according to the prior art require the addition of a considerable amount of the above additives in order to obtain practical cap-off resistance, whereby the object of the ink is reduced. It is inevitable that the adhesion to the object is reduced, and the application has been limited to the application to a marking pen for a writing board which does not require the adhesion.
【0004】[0004]
【課題を解決するための手段】本発明のマーキングペン
用インキ組成物は着色剤、樹脂、前記樹脂を溶解する有
機溶剤及び耐キャップオフ性を付与する添加剤を含有し
てなる組成である。着色剤は一般に有機溶剤系マーキン
グペンインキに用いられる有機溶剤可溶性染料(C.
I.ソルベント染料)や有機顔料及びカーボンブラッ
ク、チタン白等が用いられ、顔料では予め樹脂で表面処
理された易分散性の加工顔料が好適に用いられる。これ
ら着色剤はインキ組成中1乃至25重量%の範囲で用い
られる。The ink composition for a marking pen of the present invention is a composition containing a colorant, a resin, an organic solvent for dissolving the resin, and an additive for imparting cap-off resistance. The coloring agent is an organic solvent-soluble dye (C.I.
I. Solvent dyes), organic pigments, carbon black, titanium white, and the like are used, and as the pigment, an easily dispersible processed pigment which has been previously surface-treated with a resin is preferably used. These colorants are used in the range of 1 to 25% by weight in the ink composition.
【0005】樹脂としてはロジン、エステルガム、ロジ
ン変性マレイン酸樹脂等のロジン誘導体、ケトン樹脂、
可溶性フェノール樹脂、セルロース誘導体、スチレン−
マレイン酸共重合体、酢酸ビニル、ビニルブチラール、
ビニルピロリドン等のビニル系樹脂、フェノール変性キ
シレン樹脂、キシレン樹脂、テルペン樹脂、アクリル樹
脂、脂肪族炭化水素樹脂、脂環族炭化水素樹脂、アルキ
ッド樹脂等の一般に有機溶剤系マーキングペンインキに
用いられる樹脂がインキ組成中1乃至30重量%の範囲
で用いられる。As the resin, rosin derivatives such as rosin, ester gum, rosin-modified maleic resin, ketone resin,
Soluble phenolic resin, cellulose derivative, styrene
Maleic acid copolymer, vinyl acetate, vinyl butyral,
Resins commonly used in organic solvent-based marking pens, such as vinyl resins such as vinylpyrrolidone, phenol-modified xylene resins, xylene resins, terpene resins, acrylic resins, aliphatic hydrocarbon resins, alicyclic hydrocarbon resins, and alkyd resins Is used in the range of 1 to 30% by weight in the ink composition.
【0006】インキに耐キャップオフ性を付与するため
の添加剤は25℃乃至65℃の範囲内の融点を示すエス
テル化合物であり、具体的にはベヘニン酸オレイル(融
点38〜40℃)、オレイン酸ベヘニル(融点32〜4
2℃)、イソステアリン酸ベヘニル(融点32〜43
℃)、ラウリン酸ベヘニル(融点48〜50℃)、ステ
アリン酸ステアリル(融点58〜61℃)、やし油脂肪
酸ステアリルアルコールエステル(融点38〜48
℃)、アジピン酸ジミリスチル(融点45〜48℃)及
びブタンジオールジラウレート(融点44〜45℃)が
あげられる。前記融点範囲より低い融点を示すエステル
化合物(例えば、イソステアリン酸イソステアリル融点
0℃以下)、又はより高い融点を示すエステル化合物
〔例えば、ベヘン酸ベヘニル(融点68〜71℃)、モ
ンタン酸ベヘニル(融点68〜71℃)等〕はインキに
耐キャップオフ性を付与する機能を発揮しない。前記融
点範囲を示すエステル化合物はインキ組成中0.05乃
至0.5重量%の範囲、好ましくは0.1乃至0.4重
量%の範囲で用いられる。耐キャップオフ性は前記範囲
の添加で十分発揮され、より多量の添加はかえって耐キ
ャップオフ性を悪くするか、インキ安定性を悪くするこ
とになる。[0006] melting point indicate to Es in the additive in the range of 25 ° C. to 65 ° C. for imparting resistance to cap off properties to the ink
Teryl compounds , specifically, oleyl behenate (melting point: 38 to 40 ° C.), behenyl oleate (melting point: 32 to 4 ° C.)
2 ° C), behenyl isostearate (melting point 32-43)
C), behenyl laurate (melting point 48-50 ° C), stearyl stearate (melting point 58-61 ° C), coconut oil fatty acid stearyl alcohol ester (melting point 38-48).
C.), dimyristyl adipate (mp. 45-48.degree. C.) and butanediol dilaurate (mp. 44-45.degree. C. ) . An ester compound having a melting point lower than the melting point range (for example, isostearyl isostearate having a melting point of 0 ° C. or lower) or an ester compound having a higher melting point [for example, behenyl behenate (melting point 68 to 71 ° C.), behenyl montanate (melting point 68-71 ° C.) does not exhibit the function of imparting cap-off resistance to the ink. The ester compound having the above melting point range is used in the ink composition in the range of 0.05 to 0.5% by weight, preferably in the range of 0.1 to 0.4% by weight. The cap-off resistance is sufficiently exhibited by the addition in the above range, and the addition of a larger amount rather deteriorates the cap-off resistance or the ink stability.
【0007】溶剤はマーキングペン用インキに慣用され
る有機溶剤から前記樹脂を溶解するものが選択、適用さ
れる。具体的にはエタノール、イソプロパノール等の低
級脂肪族アルコール、プロピレングリコールモノメチル
エーテル、プロピレングリコールモノエチルエーテル等
のグリコールエーテル、酢酸ブチル、プロピオン酸エチ
ル等の低級脂肪酸エステル、ヘキサン、ヘプタン等の脂
肪族炭化水素及びキシレン等があげられ、これらが主体
溶剤として用いられる。更にプロピレングリコールモノ
エチルエーテルアセテート、エチルエトキシプロピオネ
ート、プロピオン酸ベンジル等から選ばれるエステル系
高沸点溶剤は、前記エステル化合物に対して適度の溶解
性を示し、インキ調製時エステル化合物の溶解を容易に
し、インキ中にエステル化合物を安定な溶解状態に存在
させるので前記主体溶剤と併用されてもよい。尚、全溶
剤はインキ組成中45乃至98重量%の範囲で用いられ
る。As the solvent, those which dissolve the resin from organic solvents commonly used for ink for marking pens are selected and applied. Specifically, lower aliphatic alcohols such as ethanol and isopropanol, glycol ethers such as propylene glycol monomethyl ether and propylene glycol monoethyl ether, lower fatty acid esters such as butyl acetate and ethyl propionate, and aliphatic hydrocarbons such as hexane and heptane And xylene, etc., which are used as the main solvent. Further, an ester-based high-boiling solvent selected from propylene glycol monoethyl ether acetate, ethyl ethoxypropionate, benzyl propionate, and the like shows a suitable solubility for the ester compound and facilitates dissolution of the ester compound during ink preparation. Since the ester compound is present in a stable dissolved state in the ink, it may be used in combination with the main solvent. The total solvent is used in the range of 45 to 98% by weight in the ink composition.
【0008】本発明のインキ組成物は樹脂及び添加剤を
溶剤中に混合、溶解して得られるビヒクルに着色剤を溶
解又は分散することにより調製される。The ink composition of the present invention is prepared by mixing or dissolving a resin and an additive in a solvent and dissolving or dispersing a colorant in a vehicle obtained by dissolving the colorant.
【0009】[0009]
【作 用】本発明のインキ組成物を充填したマーキング
ペンがキャップ脱着状態で放置された場合、ペン先表面
のインキの溶剤が蒸発するにつれて、インキ中の添加剤
が析出してペン先表面を覆って極薄い皮膜を形成する。
この皮膜は溶剤蒸気を透過させないが、極軽い擦過で容
易に破壊される。従って、前記皮膜がペン先表面に形成
されると、ペン先内に存在するインキ中の溶剤はそれ以
上は実質的に揮散することなく残留し、その後のマーキ
ングに際して、ペン先と対象物の擦過で前記皮膜は容易
に破れ、インキがペン先から即座に流出する。前記添加
剤は僅かの添加量で前記作用を発揮するので、マーキン
グされたインキの対象物への密着性に悪影響を及ぼすこ
とはない。[Work] When a marking pen filled with the ink composition of the present invention is left in a state where the cap is detached, as the solvent of the ink on the pen tip surface evaporates, additives in the ink precipitate and the pen tip surface is removed. Cover and form a very thin film.
This coating is impermeable to solvent vapors, but is easily destroyed by very light abrasion. Therefore, when the film is formed on the pen tip surface, the solvent in the ink present in the pen tip remains without substantially volatilizing, and during the subsequent marking, the pen tip and the object are rubbed. As a result, the film is easily broken, and the ink immediately flows out of the pen tip. Since the additive exerts the above-mentioned action with a small amount, it does not adversely affect the adhesion of the marked ink to the object.
【0010】[0010]
【実 施 例】表1に示す組成の実施例インキ及び比較
例インキを前記処方により調製した。EXAMPLES Example inks and comparative inks having the compositions shown in Table 1 were prepared according to the above-mentioned formulations.
【0011】[0011]
【表1】 [Table 1]
【0012】表中の注番号に沿って原料の内容を以下に
示す。 (1)10%のカーボンブラック、10%の樹脂及び残
余はエタノールとイソプロパノールの混合溶剤からなる
顔料分散体(オリエント化学工業(株)商品名マイクロ
ピグモAMBK) (2)バリファーストレッド1308(オリエント化学
工業(株)商品名) (3)シンセチックレジンSK(ヒュルス社商品名) (4)ラウリン酸ベヘニル 融点48〜50℃ (5)ベヘニン酸オレイル 融点38〜40℃ (6)オレイン酸ベヘニル 融点32〜42℃ (7)イソステアリン酸ベヘニル 融点32〜43℃ (8)ブタンジオールジラウレート 融点44〜45℃ (9)ヘキサグリセリンジステアレート (10)ヘキサグリセリンセスキステアレート (11)デカグリセリンペンタステアレート (12)イソステアリン酸イソステアリル 融点0℃以下 (13)モンタン酸ベヘニル 融点77〜80℃ (14)プロピレングリコールモノメチルエーテル (15)プロピレングリコールモノエチルエーテルアセテ
ートThe contents of the raw materials are shown below according to the note numbers in the table. (1) Pigment dispersion composed of 10% carbon black, 10% resin and the remainder being a mixed solvent of ethanol and isopropanol (Micropigmo AMBK, trade name of Orient Chemical Co., Ltd.) (2) Balifast Red 1308 (Orient Chemical (3) Synthetic Resin SK (trade name of Huls) (4) Behenyl laurate, melting point 48-50 ° C (5) Oleyl behenate, melting point 38-40 ° C (6) Behenyl oleate, melting point 32 -42 ° C (7) Behenyl isostearate Melting point 32-43 ° C (8) Butanediol dilaurate Melting point 44-45 ° C (9) Hexaglycerin distearate (10) Hexaglycerin sesquistearate (11) Decaglycerin pentastearate ( 12) Isostearyl isostearate Melting point 0 ° C or less (13) behenyl montanate mp 77 to 80 ° C. (14) Propylene glycol monomethyl ether (15) Propylene glycol monoethyl ether acetate
【0013】繊維束樹脂加工体からなるペン先及びチュ
ーブ状に被覆された繊維束からなるインキ吸蔵体を備え
たマーキングペンに前記試料インキを所定量充填して、
試料マーキングペンを得て、以下の試験に供した。各試
料ペンにてポリエステルフィルム上に筆記した筆跡を、
ガーゼを巻き付けた親指で約1Kgwの力をかけて10
回擦過し、筆跡の剥がれ具合からインキの密着性を評価
した。 評価 ○:変化なし ×:剥がれあり 次にキャップを外した試料ペンを、25℃,60%RH
の条件に調節した恒温恒湿室内に横置の状態で2時間放
置した後、試料ペンで紙面に筆記し、即座に筆記できる
か否かを調べた。 評価 ○:即筆記可能 ×:筆記不能 試験結果を表2に示す。A predetermined amount of the sample ink is filled in a marking pen provided with a pen tip made of a fiber bundle resin processed body and an ink occluding body made of a fiber bundle covered in a tube shape.
A sample marking pen was obtained and subjected to the following tests. The handwriting written on the polyester film with each sample pen,
Apply a force of about 1Kgw with the thumb around which the gauze is wound
It was rubbed several times, and the adhesion of the ink was evaluated from the degree of peeling of the handwriting. Evaluation :: No change ×: Peeled Next, the sample pen with the cap removed was placed at 25 ° C. and 60% RH.
After standing for 2 hours in a constant temperature and humidity room adjusted to the conditions described in (1) above, writing was performed on a sheet of paper with a sample pen, and it was examined whether or not writing was possible immediately. Evaluation :: Writable immediately ×: Not writable Table 2 shows the test results.
【0014】[0014]
【表2】 [Table 2]
【0015】[0015]
【発明の効果】本発明のインキ組成物はマーキングペン
においてキャップ脱着状態で放置された場合、ペン先で
のインキ中の溶剤の蒸発抑制作用が発揮されて、長時間
後も即座にマーキングが可能である。そして、この種の
耐キャップオフ性を具備するマーキングペンインキが呈
する対象物へのインキの密着性の低下は全くみられな
い。When the ink composition of the present invention is left in a marking pen with the cap removed, the effect of suppressing the evaporation of the solvent in the ink at the pen tip is exerted and marking can be performed immediately even after a long time. It is. Then, there is no decrease in the adhesion of the ink to the target object, which is exhibited by the marking pen ink having this kind of cap-off resistance.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平2−294372(JP,A) 特開 昭62−25184(JP,A) (58)調査した分野(Int.Cl.7,DB名) C09D 11/00 - 11/20 ────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-2-294372 (JP, A) JP-A-62-25184 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C09D 11/00-11/20
Claims (3)
溶剤及び添加剤を含有してなるインキ組成物であって、
前記添加剤は25℃乃至65℃の範囲の融点を示すラウ
リン酸ベヘニル、ベヘニン酸オレイル、オレイン酸ベヘ
ニル、イソステアリン酸ベヘニル、ステアリン酸ステア
リル、やし油脂肪酸ステアリルアルコールエステル、ア
ジピン酸ジミリスチル、ブタンジオールジラウレートか
ら選ばれるエステル化合物であり、その添加量はインキ
組成中0.05乃至0.5重量%の範囲であることを特
徴とするマーキングペン用インキ組成物。1. An ink composition comprising a colorant, a resin, an organic solvent for dissolving the resin, and an additive,
The additive Lau showing a melting point in the range of 2 5 ° C. to 65 ° C.
Behenyl phosphate, oleyl behenate, behe oleate
Nil, behenyl isostearate, stearic stearate
Ril, coconut oil fatty acid stearyl alcohol ester,
Dimyristyl dipinate, butanediol dilaurate
An ink composition for a marking pen, which is an ester compound selected from the group consisting of 0.05 to 0.5% by weight of the ink composition.
成中0.1乃至0.4重量%の範囲である請求項1記載
のマーキングペン用インキ組成物。 2. The ink composition according to claim 1, wherein the amount of said ester compound is an ink composition.
2. The composition according to claim 1, wherein the content is in the range of 0.1 to 0.4% by weight.
Ink composition for marking pens.
コールモノエチルエーテルアセテート、エチルエトキシ
プロピオネート、プロピオン酸ベンジルから選ばれるエ
ステル系高沸点溶剤である請求項1又は2記載のマーキ
ングペン用インキ組成物。 3. The method according to claim 1, wherein a part of the solvent is propylene glycol.
Coal monoethyl ether acetate, ethyl ethoxy
E selected from propionate and benzyl propionate
3. The mark according to claim 1, which is a stele-based high-boiling solvent.
Ink composition for pen.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP31270494A JP3341065B2 (en) | 1994-11-21 | 1994-11-21 | Ink composition for marking pen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP31270494A JP3341065B2 (en) | 1994-11-21 | 1994-11-21 | Ink composition for marking pen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH08170043A JPH08170043A (en) | 1996-07-02 |
| JP3341065B2 true JP3341065B2 (en) | 2002-11-05 |
Family
ID=18032429
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP31270494A Expired - Fee Related JP3341065B2 (en) | 1994-11-21 | 1994-11-21 | Ink composition for marking pen |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3341065B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5888287A (en) * | 1997-04-10 | 1999-03-30 | Markem Corporation | Washable fabrics ink |
| JP2001098197A (en) * | 1999-09-30 | 2001-04-10 | Toshiba Corp | Recording liquid and recording device |
| JP5802562B2 (en) * | 2012-01-11 | 2015-10-28 | 株式会社パイロットコーポレーション | Oil-based ink composition for marking pen and marking pen incorporating the same |
| JP2023026828A (en) * | 2021-08-16 | 2023-03-01 | 三菱鉛筆株式会社 | pencil lead |
-
1994
- 1994-11-21 JP JP31270494A patent/JP3341065B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH08170043A (en) | 1996-07-02 |
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