JPH0397776A - Oily maker ink - Google Patents
Oily maker inkInfo
- Publication number
- JPH0397776A JPH0397776A JP1232986A JP23298689A JPH0397776A JP H0397776 A JPH0397776 A JP H0397776A JP 1232986 A JP1232986 A JP 1232986A JP 23298689 A JP23298689 A JP 23298689A JP H0397776 A JPH0397776 A JP H0397776A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- ink
- oil
- additive
- handwriting
- 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.)
- Pending
Links
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は油性マーカーに使用するインキ組成物に関し、
更に詳細にはガラス、金属、樹脂等の非吸収性の筆記面
における筆跡の定着性に優れた油性インキに関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an ink composition for use in oil-based markers,
More specifically, the present invention relates to an oil-based ink that is excellent in fixing handwriting on non-absorbent writing surfaces such as glass, metal, and resin.
従来の油性マーカーはガラス、金属、樹脂などの非吸収
面に筆記した場合、筆跡の定着性が弱く、筆跡を布・紙
等で擦堝した場合、筆跡が消去されてしまうという欠点
を有していた。Conventional oil-based markers have the disadvantage that when written on non-absorbent surfaces such as glass, metal, or resin, the handwriting does not stick well, and when the handwriting is rubbed with cloth, paper, etc., the handwriting is erased. was.
本発明は、従来の油性マーカーインキの非吸収面に対す
る筆跡の定着性をより優れたものとし、あらゆる非吸収
面に対して擦堝しても筆跡が消えることなく、初期の筆
跡を維持できる油性マーカーインキを提供するものであ
る。The present invention improves the fixation of handwriting on non-absorbing surfaces of conventional oil-based marker inks, and provides an oil-based marker ink that maintains the initial handwriting without erasing even when rubbed against any non-absorbing surface. The company provides marker ink.
上記目的を達成するために、本発明は着色剤、樹脂及び
有機溶剤に、添加剤として少なくとも力ルボキシル化ポ
リオキシエチレンアルキルエーテルを添加することを特
徴とした油性インキである。In order to achieve the above object, the present invention is an oil-based ink characterized in that at least a carboxylated polyoxyethylene alkyl ether is added as an additive to a colorant, a resin, and an organic solvent.
以下本発明の各成分について説明する6本発明に用いる
着色剤としては有機溶剤に可溶な酸性染料、合金染料、
塩基性染料などが用いられる。又、顔料も用いることが
できる。例えば、染料ではオイル1ノツド5B(オリエ
ント化学工業O困製)、バリファストブルー#2606
(同」二)、バリファストレッド#2303、#33
04 (同上)、スピロンレツドGEH,BEH(保土
谷化学工業■製)、ローダミン、メチルバイオレットな
どが挙げられる。更に顔料としては、無機顔料、有機顔
料共に使用することができ、例えばカーボンブラック、
酸化チタン、鉄黒、ベンガラやアゾ、フタロシアニン、
アンスラキノン、インジゴ、トリフエニルメタン、キサ
ンタン系などが挙げられる。Each component of the present invention will be explained below.6 Coloring agents used in the present invention include acid dyes, alloy dyes, and soluble dyes in organic solvents.
Basic dyes and the like are used. Pigments can also be used. For example, dyes such as Oil 1 Nod 5B (manufactured by Orient Chemical Industry Co., Ltd.), Varifast Blue #2606
(same" 2), Bali Fast Red #2303, #33
04 (same as above), Spiron Red GEH, BEH (manufactured by Hodogaya Chemical Industry ■), rhodamine, and methyl violet. Furthermore, both inorganic pigments and organic pigments can be used as pigments, such as carbon black,
titanium oxide, iron black, red iron oxide, azo, phthalocyanine,
Examples include anthraquinone, indigo, triphenylmethane, and xanthan.
これらの着色剤は単独で用いても良いし、2種類以上混
合しても構わない。配合量については特に制限はなく、
その範囲は広く通常1〜50重量%の範囲で用いられる
。These colorants may be used alone or in a mixture of two or more. There are no particular restrictions on the amount of compounding.
Its range is wide, and it is usually used in the range of 1 to 50% by weight.
樹脂としては着色剤と同様、有機溶剤に可溶な油溶性樹
脂が用いられる。例えばロジン、エステルガム、ロジン
変性マレイン酸レジン等のロジン誘導体、ケトン樹脂、
フェノール樹脂、アクリル/スチレン系樹脂、スチレン
マレイン酸樹脂などが挙げられる。溶剤状態はもちろん
エマルジョン状態でも構わない。配合量はこの場合もと
くに制限はなく、通常インキ組成中1〜30重量%の範
囲で用いられる。As the resin, an oil-soluble resin soluble in an organic solvent is used, similar to the colorant. For example, rosin, ester gum, rosin derivatives such as rosin-modified maleic acid resin, ketone resin,
Examples include phenol resin, acrylic/styrene resin, styrene maleic acid resin, and the like. It may be in a solvent state or an emulsion state. In this case as well, there is no particular restriction on the blending amount, and it is usually used in the range of 1 to 30% by weight in the ink composition.
有機溶剤としては、メタノール、エタノール等の低級脂
肪族アルコール類、酢酸メチル、酢酸エチル等のエステ
ル類、メチルセロソルブ、エチルセロソルブ、プロピレ
ングリコールモノメチルエーテル等のグリコールエーテ
ル類、アセトン、MEK等のケトン類の有機溶剤が使用
でき、配合量はインキ組成中20〜98重量%の範囲で
用いられる。Examples of organic solvents include lower aliphatic alcohols such as methanol and ethanol, esters such as methyl acetate and ethyl acetate, glycol ethers such as methyl cellosolve, ethyl cellosolve, and propylene glycol monomethyl ether, and ketones such as acetone and MEK. Organic solvents can be used, and the amount used is in the range of 20 to 98% by weight in the ink composition.
添加剤であるカルボキシル化ポリオキシエチレンアルキ
ルエーテルについて述べると、(一般式)
R − 0 ( C H .C H , O ) ,
,C H , G O O M(式中nは1〜20の自
然数、RはC1〜C I 6のアルキル基を、MはH原
子、NaやKなどの金属原子またはアンモニウムまたは
アルカノールアミンを表す)で示されて、筆跡の定着性
を向上させるために使用するもので、例えばカルボキシ
ル化トリオキシエチレンラウリルエーテル、カルボキシ
ル化へキサオキシエチレンエチルエーテル等が挙げられ
る。添加量は着色剤や樹脂の量により異なるが、0.5
〜7重量%が好ましい。これ以上の添加は逆効果を示し
定着性を悪くする。Regarding carboxylated polyoxyethylene alkyl ether, which is an additive, (general formula) R-0 (CH.CH, O),
, C H , G O O M (in the formula, n is a natural number of 1 to 20, R is an alkyl group of C1 to C I 6, M is an H atom, a metal atom such as Na or K, or ammonium or an alkanolamine) ) and are used to improve the fixation of handwriting, such as carboxylated trioxyethylene lauryl ether and carboxylated hexaoxyethylene ethyl ether. The amount added varies depending on the amount of colorant and resin, but 0.5
~7% by weight is preferred. Addition of more than this has the opposite effect and worsens the fixing properties.
本発明組成物においては前記必須成分に加え、通常油性
インキに用いられる他の添加剤、例えば、粘度調整剤、
可塑剤、分散剤などを必要に応じて添加することも可能
である。In addition to the above-mentioned essential components, the composition of the present invention may contain other additives commonly used in oil-based inks, such as viscosity modifiers,
It is also possible to add plasticizers, dispersants, etc. as necessary.
[作用1
油性マーカーでガラス、金属、樹脂等の非吸収面に筆記
した場合、筆跡の定着性が悪く、布・紙等の擦堝で筆跡
が消去してしまったが、本発明のカルボキシル化ポリオ
キシエチレンアルキルエーテルを添加したインキを用い
ると、樹脂あるいは筆記表面が改質されることにより樹
脂と非吸収性の表面との吸着性が強くなり、非吸収面に
筆記した場合、筆跡を擦堝しても消去されることなく、
油性マーカーの定着性をより優れたものとしている。[Effect 1: When writing with a permanent marker on a non-absorbing surface such as glass, metal, resin, etc., the handwriting has poor fixation and is erased by rubbing cloth, paper, etc., but the carboxylation of the present invention When ink containing polyoxyethylene alkyl ether is used, the resin or writing surface is modified, so that the adsorption between the resin and the non-absorbent surface becomes stronger, and when writing on a non-absorbent surface, the handwriting will not be rubbed off. It will not be erased even if it is washed away,
Improves the fixing properties of oil-based markers.
〔実施例]
本発明の実施例を比較例と対比してその特長を説明する
。なお、(部)は重量部を示す。[Example] Examples of the present invention will be compared with comparative examples to explain their features. Note that (parts) indicates parts by weight.
樹脂
・マルキード 34 (荒川化学工業(株製)溶剤
・イソプロビルアルコール
添加剤 ・C,H,,−0−(04,CH,O).−C
I{,COONa5 〃
34 II
l n
溶剤
・エチルセロソルブ
83〃
・ベンジルアルコール
l 〃
添加剤 − C,H,−0−(CI,CI,0),.−
CII,COOHl u
溶剤 ・キシレン
添加剤 ・C,H, 1(1−(CH、C}+, O)
1(M,COOK樹脂 ・マルキード 34 (荒
川化学工業(+′1製)溶剤 ・イソブロビルアルコ
ール
比較謂一−2−
80(部)
5 〃
5 n
85〃
筆記し、筆跡の[η着性の評価試験を行った。その結果
は下表の通りである。Resin/Marquid 34 (Arakawa Chemical Industry Co., Ltd.) Solvent
・Isopropyl alcohol additive ・C,H,,-0-(04,CH,O). -C
I{, COONa5 〃 34 II l n Solvent・Ethyl cellosolve 83〃・Benzyl alcohol l 〃 Additive - C, H, -0-(CI, CI, 0),. −
CII, COOHl u Solvent ・Xylene additive ・C, H, 1 (1-(CH, C}+, O)
1 (M, COOK resin ・Malquid 34 (manufactured by Arakawa Chemical Industries (+'1) solvent ・Isobrobyl alcohol comparison 1-2- 80 (parts) 5 〃 5 n 85 〃 Handwriting [η adhesion An evaluation test was conducted.The results are shown in the table below.
なお、ここで行った固着性の評価試験は、メタノールで
洗浄した非吸収表面に筆記し、1[](24時間)室温
に放置後、綿棒で擦堝し、非吸収表面が露出するまでの
回数で評価した。The adhesion evaluation test conducted here was performed by writing on a non-absorbing surface that had been cleaned with methanol, leaving it at room temperature for 1[] (24 hours), then rubbing it with a cotton swab until the non-absorbing surface was exposed. Evaluated by number of times.
表
溶剤
・エチルセロソルブ
・ベンジルアルコール
84〃
l 〃
溶剤
・キシレン
85
上記各実施例の油住マーカーインキと比較例の油性マー
カーインキを、ガラス、金属、樹脂板に但し、◎は特に
良好、○は良好、△はやや劣る、×は劣る〔発明の効果
]
上記評価試験結果においても、本発明による油性マーカ
ーインキ(実施例l、実施例2、実施例3)はガラス、
金属、樹脂に筆記した筆跡の固着性は良好あるいは特に
良好の結果を得、比較した添加剤として、カルボキシル
化ポリオキシエチレンアルキルエーテルを含まないイン
キに比して優れている。Surface solvent: ethyl cellosolve, benzyl alcohol 84 l Solvent: xylene 85 The oil-based marker ink of each of the above examples and the oil-based marker ink of the comparative example were applied to glass, metal, and resin plates. Good, △ is slightly inferior, × is inferior [Effect of the invention] Also in the above evaluation test results, the oil-based marker ink according to the present invention (Example 1, Example 2, Example 3) was good for glass,
Good or particularly good results were obtained for the adhesion of handwriting written on metals and resins, and it is superior to inks that do not contain carboxylated polyoxyethylene alkyl ether as compared additives.
本発明の油性マーカーインキは非吸収面に対する筆跡の
定符性をより優れたものとし、非吸収面の筆跡を擦堝し
ても消えるこ辷なく、初期の筆跡が維持できる効果を有
する。The oil-based marker ink of the present invention improves the consistency of handwriting on a non-absorbing surface, and has the effect that even when handwriting on a non-absorbing surface is rubbed, it does not fade and the initial handwriting can be maintained.
Claims (1)
も下記の一般式で示されるカルボキシル化ポリオキシエ
チレンアルキルエーテルを含有してなることを特徴とす
る油性マーカーインキ。 (一般式) R−O−(CH_2CH_2O)_nCH_2COOM
式中nは1〜20の自然数、RはC_2〜C_2_0の
アルキル基を、MはH原子、NaやKなどの金属原子ま
たはアンモニウムまたはアルカノールアミンを表す。[Scope of Claims] An oil-based marker ink characterized by containing at least a carboxylated polyoxyethylene alkyl ether represented by the following general formula as an additive in a colorant, a resin, and an organic solvent. (General formula) R-O-(CH_2CH_2O)_nCH_2COOM
In the formula, n is a natural number from 1 to 20, R represents an alkyl group of C_2 to C_2_0, and M represents an H atom, a metal atom such as Na or K, or ammonium or an alkanolamine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1232986A JPH0397776A (en) | 1989-09-11 | 1989-09-11 | Oily maker ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1232986A JPH0397776A (en) | 1989-09-11 | 1989-09-11 | Oily maker ink |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0397776A true JPH0397776A (en) | 1991-04-23 |
Family
ID=16948006
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1232986A Pending JPH0397776A (en) | 1989-09-11 | 1989-09-11 | Oily maker ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0397776A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6814791B2 (en) * | 2000-09-29 | 2004-11-09 | Domino Printing Sciences Plc | Ink jet printing compositions and methods |
-
1989
- 1989-09-11 JP JP1232986A patent/JPH0397776A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6814791B2 (en) * | 2000-09-29 | 2004-11-09 | Domino Printing Sciences Plc | Ink jet printing compositions and methods |
US7147699B2 (en) * | 2000-09-29 | 2006-12-12 | Domino Printing Sciences Plc | Ink jet printing compositions and methods |
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