JPS59184270A - Printing ink - Google Patents

Printing ink

Info

Publication number
JPS59184270A
JPS59184270A JP58059098A JP5909883A JPS59184270A JP S59184270 A JPS59184270 A JP S59184270A JP 58059098 A JP58059098 A JP 58059098A JP 5909883 A JP5909883 A JP 5909883A JP S59184270 A JPS59184270 A JP S59184270A
Authority
JP
Japan
Prior art keywords
solvent
binder
printing ink
particles
good solvent
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
JP58059098A
Other languages
Japanese (ja)
Other versions
JPS642636B2 (en
Inventor
Mamoru Kamiyama
上山 守
Hideji Kuwajima
秀次 桑島
Shozo Yamana
章三 山名
Takao Yamada
隆男 山田
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.)
Resonac Corp
Original Assignee
Hitachi Chemical 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP58059098A priority Critical patent/JPS59184270A/en
Publication of JPS59184270A publication Critical patent/JPS59184270A/en
Publication of JPS642636B2 publication Critical patent/JPS642636B2/ja
Granted legal-status Critical Current

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  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

PURPOSE:To provide a printing ink which has excellent levelability and improved thixotropic properties so that no sagging is caused, by mixing particles, an org. binder and a mixture of a good solvent and a poor solvent for said binder in a specified weight ratio. CONSTITUTION:Particles (A) having a particle size of pref. 20mum or below, such as pigment, metallic particles or glass powder, an org. binder (B) such as ethyl- celluloe or acrylic resin, and a solvent mixture (C) obtd. by mixing a good solvent (e.g. butylcarbitol or carbitol acetate) for said binder and a poor solvent (e.g. terpineol or polyethylene glycol) for said binder in a weight ratio of 10/90- 90/10, are mixed together to obtain the desired printing ink. The resulting ink does not cause sagging observed when a good solvent alone is used, nor unevenness of the surface observed when a poor solvent alone is used.

Description

【発明の詳細な説明】 本発明は印刷インクの改良に関する。[Detailed description of the invention] The present invention relates to improvements in printing inks.

従来印刷インクは有機結合剤に対し良溶媒が使用されて
おり、この良溶媒の含有量により粒子の含有量が調節さ
れていた。
Conventionally, printing inks have used a good solvent for an organic binder, and the content of particles has been controlled by the content of this good solvent.

良溶媒のみを使用した場合には、渋面の平滑さすなわち
レベリング性は向上するが印刷されたパターンのダレな
どが発生する欠点があった。
When only a good solvent is used, the smoothness of the rough surface, that is, the leveling property is improved, but there is a drawback that the printed pattern sag occurs.

これを防ぐ方法として、シキソトロピー(揺変性)を向
上させるためエーロゾルなどの微粉を添加する方法があ
るが9例えばセラミック用印刷インクなどでは、不純物
の添加になるため焼結特性が変化するなとの欠点があっ
た。
One way to prevent this is to add fine powder such as aerosol to improve thixotropy.9 For example, in printing ink for ceramics, it is important not to change the sintering properties because it adds impurities. There were drawbacks.

本発明はこれらの欠点を解決した印刷インクを提供する
ことを目的とするものである。
The object of the present invention is to provide a printing ink that overcomes these drawbacks.

本発明者らは従来良溶媒のみを用いた場合に表われるシ
キソトロピーの低下を解決する方法について鋭意検討し
た結果、理由は定かではないが良溶媒の一部を有機結合
剤に対し貧溶媒で代替することによりシキソトロピーを
高めることが出き。
The inventors of the present invention have conducted intensive studies on methods to resolve the decrease in thixotropy that appears when conventionally using only good solvents, and found that, although the reason is not clear, some of the good solvents were replaced with poor solvents for organic binders. By doing so, the xixotropy can be increased.

良溶媒によるレベリング性を維持しながらかつシキソト
ロビーによるダレの防止が出きることを見いだした。
It has been found that it is possible to prevent sagging due to xyxothrobby while maintaining leveling properties due to a good solvent.

本発明は粒子、有機結合剤及び溶媒からなり溶媒が有機
結合剤に対し良溶媒と貧溶媒の混合溶媒でbす、かつ良
溶媒/貧溶媒のN量比が10/90乃至90/10であ
る印刷インクに関する。
The present invention consists of particles, an organic binder, and a solvent, and the solvent is a mixed solvent of a good solvent and a poor solvent for the organic binder, and the N amount ratio of the good solvent/poor solvent is 10/90 to 90/10. Concerning a certain printing ink.

本発明における粒子とは顔料、金属粒子、ガラス等の無
機粒子などで1何ら制限するものではない。しかし印刷
インクに使用する目的上、その粒子の大きさは20μm
以下が好ましく、10μm以下がさらに好ましい。有機
結合剤としてはエチルセルローズ、ブチラール樹脂、ア
クリル樹脂などが用いられ、又その添加量は特に制限は
ないが粒子100重量部に対し0.5〜20重量部添加
することが好ましく、1〜10重量部添加すればさらに
好ましい。
Particles in the present invention include pigments, metal particles, inorganic particles such as glass, etc., and are not limited in any way. However, for the purpose of using it in printing ink, the particle size is 20 μm.
The thickness is preferably 10 μm or less, and more preferably 10 μm or less. As the organic binder, ethyl cellulose, butyral resin, acrylic resin, etc. are used, and the amount added is not particularly limited, but it is preferably added in an amount of 0.5 to 20 parts by weight, and 1 to 10 parts by weight per 100 parts by weight of particles. It is more preferable to add part by weight.

本発明における良溶媒とは熱力学的相互作用係数が0.
4〜0.5で溶解性に優れた溶媒をさしブチルカルピト
ール、カルピトールアセテートなどがアシ、又貧溶媒と
は熱力学的相互作用係数が0.3〜0.4未満で溶解性
の悪い溶媒をさしテレピネオール、ポリエチレングリコ
ール、ポリプロピレングリコールなどがある。その沸点
、粘度などは特に制限はないが印刷インクに使用する必
要上、沸点は100℃以上が好ましく’、150℃以上
であればさらに好ましい。
In the present invention, a good solvent has a thermodynamic interaction coefficient of 0.
Solvents with a thermodynamic interaction coefficient of 4 to 0.5 and excellent solubility are referred to as butyl carpitol, carpitol acetate, etc., and poor solvents are those with a thermodynamic interaction coefficient of less than 0.3 to 0.4 and excellent solubility Examples of bad solvents include terpineol, polyethylene glycol, and polypropylene glycol. There are no particular restrictions on its boiling point, viscosity, etc., but in view of the need for use in printing ink, the boiling point is preferably 100°C or higher, and more preferably 150°C or higher.

良溶媒と貧溶媒は互いに相溶することぶ望ましい。良溶
媒と貧溶媒の混合比率、すなわち良溶媒/貧溶媒の重量
比が10/90乃至90/10であることが必要であり
、この範囲から外れると性質の異なった溶媒を混合した
効果がなく良溶媒がこの範囲より多い場合はレベリング
性は良いがシキソトロピーがないため印刷後にダレが生
じやすい。又貧溶媒がこの範囲より多い場合はシキソト
ロピーは良くダレが生じないが、レベリング性が悪く、
印刷表面の凹凸がひどくなる。
It is desirable that the good solvent and the poor solvent be compatible with each other. It is necessary that the mixing ratio of good solvent and poor solvent, that is, the weight ratio of good solvent/poor solvent, is between 10/90 and 90/10; if it is outside this range, the effect of mixing solvents with different properties will be lost. When the amount of the good solvent exceeds this range, leveling properties are good, but sag is likely to occur after printing due to lack of thixotropy. If the amount of the poor solvent exceeds this range, the xixotropy will be good and no sagging will occur, but the leveling property will be poor and
The unevenness of the printing surface becomes severe.

又貧溶媒と良溶媒の粘度は特に制限するものではないが
貧溶媒が良溶媒より高粘性であることが望ましい。
Although the viscosity of the poor solvent and the good solvent is not particularly limited, it is desirable that the poor solvent has a higher viscosity than the good solvent.

以下実施例により本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1 平均粒径1.8μmのタングステン粒子100重量部(
日本タングステン■製)、有機結合剤としてエチルセル
ローズ3重量部、可塑剤としてフタル酸エステル1.5
M量部、さらに溶媒として良溶媒であるブチルカルピト
ールと貧溶媒であるテレピネオールを重量比で20/8
0(ブチルカルピトール/テレピネオール)に混合した
混合溶媒を40重量部添加し3ネロールで混合し印刷イ
ンクを得た。
Example 1 100 parts by weight of tungsten particles with an average particle size of 1.8 μm (
(manufactured by Nippon Tungsten ■), 3 parts by weight of ethyl cellulose as an organic binder, and 1.5 parts of phthalate as a plasticizer.
Part M, and a weight ratio of butylcarpitol, which is a good solvent, and terpineol, which is a poor solvent, is 20/8 as a solvent.
A printing ink was obtained by adding 40 parts by weight of a mixed solvent of 0 (butylcarpitol/terpineol) and mixing with 3 nerol.

次いでこれをライン〜ライン間隔100μmのスクリー
ンを使用してセラミックグリーンシートに印刷した。
This was then printed on a ceramic green sheet using a screen with a line-to-line spacing of 100 μm.

印刷品の断面及び表面を日本光学製実体顕微鏡で観察し
たがインクのダレもなく、父表面も平滑であった。
When the cross section and surface of the printed product were observed using a stereomicroscope manufactured by Nippon Kogaku, there was no ink dripping and the surface was smooth.

実施例2 実施例1と同じタングステン粒子、有機結合剤及び可塑
剤を実施例1と同量配合し、これに良溶媒と貧溶媒を重
量比で80/20(ブチルカルピトール/テレピネオー
ル)に混合した混合溶媒を35重量部添加し3本ロール
で混合して印刷インクを得た。
Example 2 The same tungsten particles, organic binder, and plasticizer as in Example 1 were blended in the same amount as in Example 1, and a good solvent and a poor solvent were mixed in a weight ratio of 80/20 (butylcarpitol/terpineol). 35 parts by weight of the mixed solvent prepared above were added and mixed using three rolls to obtain a printing ink.

次いでこれをライン〜ライン間隔100μmのスクリー
ンを使用してセラミックグリーンシートに印刷した。
This was then printed on a ceramic green sheet using a screen with a line-to-line spacing of 100 μm.

印刷品の断面及び表面を日本光学製実体顕微鏡で観察し
たがインクのダレもなく、父表面も平滑であった。
When the cross section and surface of the printed product were observed using a stereomicroscope manufactured by Nippon Kogaku, there was no ink dripping and the surface was smooth.

比較例1 実施例1と同じタングステン粒子、有機結合剤及び可塑
剤を実施例1と同量配合し、これにブチルカルピトール
を溶媒として35重量部添加し3本ロールで混合して印
刷インクを得た。
Comparative Example 1 The same tungsten particles, organic binder, and plasticizer as in Example 1 were blended in the same amount as in Example 1, and 35 parts by weight of butyl calpitol was added as a solvent and mixed with three rolls to form a printing ink. Obtained.

次いでこれ全ライン〜ライン間隔100μmのスクリー
ンを使用してセラミックグリーンシートに印刷した。
Next, this was printed on a ceramic green sheet using a screen with a line spacing of 100 μm from all lines.

印刷品の断面及び表面を日本光学製実体顕微鏡で観察し
たところ表面は極めて平滑であったが。
When the cross section and surface of the printed product were observed using a stereomicroscope manufactured by Nippon Kogaku, the surface was found to be extremely smooth.

インクのダレが見られライン〜ライン間隔が100μn
1から20乃至50μmにまで狭くなっており。
Ink dripping is visible and line-to-line spacing is 100 μn
It becomes narrower from 1 to 20 to 50 μm.

一部短絡もみられた。Some short circuits were also observed.

比較例2 実施例1と同じタングステン粒子、有機結合剤及び可塑
剤を実施例1と同量配合し、これにテレピネオールを溶
媒として45重量部添加し3ネロールで混合して印刷イ
ンクを得た。
Comparative Example 2 The same tungsten particles, organic binder, and plasticizer as in Example 1 were blended in the same amounts as in Example 1, and 45 parts by weight of terpineol as a solvent was added thereto and mixed with 3 nerol to obtain a printing ink.

次いでこれをライン〜ライン間隔100μmのスクリー
ンを使用してセラミックグリーンシートに印刷した。
This was then printed on a ceramic green sheet using a screen with a line-to-line spacing of 100 μm.

印刷品の断面及び表面を日本光学製実体顕微鏡で観察し
たところ表面はスクリーンのメツシュのあとがみられ平
滑ではなく、印刷ラインの厚さが不均一であった。
When the cross section and surface of the printed product were observed using a stereomicroscope manufactured by Nippon Kogaku, the surface was not smooth with marks from the screen mesh, and the thickness of the printed lines was uneven.

本発明になる印刷インクは粒子、有機結合剤及び溶媒か
らなり、溶媒が良溶媒と貧溶媒との混合溶媒であり、か
つ良溶奴/貧浴媒のMM、比が1゜/90乃至90/1
0としたので良溶媒のみにおけるダレもなく、又貧溶媒
のみによる表面の凹凸もなく、レベリング性とシキソト
ロビーヲ兼ね合わせることができる。
The printing ink of the present invention consists of particles, an organic binder, and a solvent, and the solvent is a mixed solvent of a good solvent and a poor solvent, and the MM ratio of good solvent/poor solvent is 1°/90 to 90. /1
Since it is set to 0, there is no sag due to only a good solvent, and there is no surface unevenness due only to a poor solvent, and both leveling properties and xyxotrope can be achieved.

代理人 弁理士 若 林 邦 彦、−゛111.ノAgent: Patent attorney Kunihiko Wakabayashi, -゛111. of

Claims (1)

【特許請求の範囲】[Claims] 1、粒子、有機結合剤及び溶媒からなシ、溶媒が有機結
合剤に対し良溶媒と貧溶媒との混合溶媒であり、かつ良
溶媒/貧溶媒の重量比が10/90乃至90/10であ
る印刷インク。
1. Particles, an organic binder, and a solvent.The solvent is a mixed solvent of a good solvent and a poor solvent for the organic binder, and the weight ratio of good solvent/poor solvent is 10/90 to 90/10. Some printing ink.
JP58059098A 1983-04-04 1983-04-04 Printing ink Granted JPS59184270A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58059098A JPS59184270A (en) 1983-04-04 1983-04-04 Printing ink

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58059098A JPS59184270A (en) 1983-04-04 1983-04-04 Printing ink

Publications (2)

Publication Number Publication Date
JPS59184270A true JPS59184270A (en) 1984-10-19
JPS642636B2 JPS642636B2 (en) 1989-01-18

Family

ID=13103513

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58059098A Granted JPS59184270A (en) 1983-04-04 1983-04-04 Printing ink

Country Status (1)

Country Link
JP (1) JPS59184270A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0607911A2 (en) * 1993-01-22 1994-07-27 Mikuni Shikiso Kabushiki Kaisha Waterbased ink composition for ink-jet printing

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56166276A (en) * 1980-05-27 1981-12-21 Kao Corp Printing ink
JPS5751435A (en) * 1980-09-13 1982-03-26 Matsushita Electric Works Ltd Gate structure in metallic mold

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56166276A (en) * 1980-05-27 1981-12-21 Kao Corp Printing ink
JPS5751435A (en) * 1980-09-13 1982-03-26 Matsushita Electric Works Ltd Gate structure in metallic mold

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0607911A2 (en) * 1993-01-22 1994-07-27 Mikuni Shikiso Kabushiki Kaisha Waterbased ink composition for ink-jet printing
EP0607911A3 (en) * 1993-01-22 1994-10-26 Mikuni Color Works Waterbased ink composition for ink-jet printing.

Also Published As

Publication number Publication date
JPS642636B2 (en) 1989-01-18

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