JP2003155428A - Drying agent for printing ink - Google Patents
Drying agent for printing inkInfo
- Publication number
- JP2003155428A JP2003155428A JP2001392830A JP2001392830A JP2003155428A JP 2003155428 A JP2003155428 A JP 2003155428A JP 2001392830 A JP2001392830 A JP 2001392830A JP 2001392830 A JP2001392830 A JP 2001392830A JP 2003155428 A JP2003155428 A JP 2003155428A
- Authority
- JP
- Japan
- Prior art keywords
- cobalt
- solution
- printing ink
- viscosity
- octylate
- 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
Links
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
【発明の詳細な説明】
【0001】
【発明の属する技術分野】この発明は、コバルト石鹸溶
液からなる印刷インキ用乾燥剤であって、とくに金属含
有量が高く、印刷用インキと同等の粘度を有する印刷イ
ンキ用乾燥剤に関するものである。
【0002】
【従来の技術】コバルト石鹸は、インキ添加剤、塗料添
加剤、合成用触媒、プラスチック添加剤などとして使用
され、乾燥剤、硬化促進剤として重要な機能を発揮する
ものである。しかしコバルト金属の高含有量のコバルト
石鹸は、固体の状態、または高粘度であって流動性に乏
しいため、そのまま流動性の高い印刷用インキの乾燥剤
として使用する場合、加温することによって流動性を高
めたり、トルエン、キシレン、あるいは鉱物油などの溶
剤を用いて流動性を高めて使用されている。さらにその
ような溶剤を使用しても、所定の粘度まで流動性を高め
ることが困難なときには、その溶剤量を多くするとか、
粘度低下剤を添加して調整を行っている。これらの溶剤
や、粘度低下剤などの添加物を使用すると、印刷用イン
キの物性を変化させる原因となり好ましくない。また昨
今の環境問題の拡がりによって、溶剤、とくに揮発性有
機化合物の使用を抑制することが望まれている現状にあ
る。
【0003】
【発明が解決しようとする課題】この発明は、印刷用イ
ンキの乾燥剤として、印刷用インキに混合することによ
り相溶性が高く、そのために作業性に優れ、また貯蔵し
た際に安定性のあるコバルト石鹸溶液からなる印刷イン
キ用乾燥剤を得ることを目的とする。
【0004】
【課題を解決するための手段】 オクチル酸コバルト
に、炭素数が8〜10の有機カルボン酸を添加し、コバ
ルト金属が10〜14%含有したところのオクチル酸コ
バルト溶液を、30度Cにおいて20〜500ポイズの
粘度に調整したオクチル酸コバルト溶液からなることを
特徴とする印刷インキ用乾燥剤とする。
【0005】
【発明の実施の形態】コバルト石鹸溶液に炭素数が8〜
10の有機カルボン酸を添加する。とくに望ましくは反
応系の薬剤であるオクチル酸を添加することによって、
金属含有量をあまり低下させることなく、所定の粘度の
制御を行うことができ、保存安定性のよい印刷インキ用
の乾燥剤となる製品を得ることができる。そしてこれに
より、溶剤として芳香族系化合物の使用も無くすること
ができることとなる。前述の有機カルボン酸としては、
ネオデカン酸、オクチル酸、カプリル酸、カプリン酸、
ノナン酸、セカノイック酸などである。これらにおいて
炭素数が7以下では臭気が強くて適当ではなく、炭素数
が11以上では常温で固体となり、前述のように炭素数
が8〜10の有機カルボン酸が適当である。つぎに実施
例と比較例を挙げて説明する。
【0006】実施例1;オクチル酸317gを計り取
り、1リットルセパラブルフラスコに入れ、攪拌しなが
ら塩基性炭酸コバルト(コバルト含有量45%)130
gを加えた。急激な炭酸ガスの発生を抑制するために、
反応温度を徐々に上げていき、100度Cに達した時点
で反応温度の上昇を止め、攪拌を続けつつ、1時間その
温度を保持した。続いて、反応中に生成した水を除去す
るために、温度を140度Cまで上昇させ、攪拌を続け
つつ、一時間その温度を保持した。つぎにオクチル酸1
13gを投入し、70度Cまで冷却して、オクチル酸コ
バルト溶液480gを得た。オクチル酸コバルト溶液の
コバルト含有量は、12.3%であり、溶液の粘度は2
60ポイズであった。一週間後にこの溶液の粘度を測定
したところ、260ポイズ(30度C)であり、変化は
無かった。
【0007】実施例2;オクチル酸317gを計り取
り、1リットルセパラブルフラスコに入れ、攪拌しなが
ら25%水酸化ナトリウム水溶液160gを加えて、オ
クチル酸ナトリウムを生成させた。この溶液を60度C
に保持し、コバルト濃度を100g/リットルに調整し
た硫酸コバルト水溶液590ミリリットルを30分かけ
て加え、オクチル酸コバルトを生成させた。このときに
副生した硫酸ナトリウムは水洗によって除去した。得ら
れたオクチル酸コバルト溶液を140度Cまで加熱し、
含まれている水分を除去した。つぎにオクチル酸113
gを投入し、オクチル酸コバルト溶液470gを得た。
オクチル酸コバルト溶液のコバルト含有量は、12.4
%であり、溶液の粘度は280ポイズ(30度C)であ
った。一週間後にこの溶液の粘度を測定したところ、2
80ポイズ(30度C)であり、変化は無かった。
【0008】実施例3;オクチル酸317gを計り取
り、1リットルセパラブルフラスコに入れ、攪拌しなが
ら25%水酸化ナトリウム水溶液160gを加えて、オ
クチル酸ナトリウムを生成させた。この溶液を60度C
に保持し、コバルト濃度を100g/リットルに調整し
た硫酸コバルト水溶液590ミリリットルを30分かけ
て加え、オクチル酸コバルトを生成させた。このときに
副生した硫酸ナトリウムは水洗によって除去した。得ら
れたオクチル酸コバルト溶液を140度Cまで加熱し、
含まれている水分を除去した。つぎにオクチル酸143
gを投入し、オクチル酸コバルト溶液500gを得た。
オクチル酸コバルト溶液のコバルト含有量は、11.8
%であり、溶液の粘度は140ポイズ(30度C)であ
った。一週間後にこの溶液の粘度を測定したところ、1
40ポイズ(30度C)であり、変化は無かった。
【0009】比較例1:オクチル酸の代わりに、石油系
溶剤を使用して粘度低下を試みたが、固体状であって、
流動性のものが得られなかった。すなわちオクチル酸3
17gを計り取り、1リットルセパラブルフラスコに入
れ、攪拌しながら25%水酸化ナトリウム水溶液160
gを加えて、オクチル酸ナトリウムを生成させた。この
溶液に日本石油株式会社製溶剤アロマフリーソルベント
6号(AF−6)123gを加え、60度Cに保持し、
コバルト濃度を100g/リットルに調整した硫酸コバ
ルト水溶液590ミリリットルを30分かけて加え、オ
クチル酸コバルトを生成させた。このときに副生した硫
酸ナトリウムは水洗によって除去した。得られたオクチ
ル酸コバルト溶液を140度Cまで加熱し、含まれてい
る水分を除去し、オクチル酸コバルト溶液490gを得
た。オクチル酸コバルト溶液のコバルト含有量は、1
2.1%であったが、溶液の粘度は30度Cまで冷却す
ると固化した。
【0010】比較例2:比較例1の条件で、粘度低下剤
を少量添加した。添加直後の粘度は低かったが、一週間
ほどで相分離が起こり、経時的に不安定であった。すな
わちオクチル酸317gを計り取り、1リットルセパラ
ブルフラスコに入れ、攪拌しながら25%水酸化ナトリ
ウム水溶液160gを加えて、オクチル酸ナトリウムを
生成させた。この溶液に日本石油株式会社製溶剤アロマ
フリーソルベント6号(AF−6)123gを加え、6
0度Cに保持し、コバルト濃度を100g/リットルに
調整した硫酸コバルト水溶液590ミリリットルを30
分かけて加え、オクチル酸コバルトを生成させた。この
ときに副生した硫酸ナトリウムは水洗によって除去し
た。得られたオクチル酸コバルト溶液を140度Cまで
加熱し、含まれている水分を除去し、オクチル酸コバル
ト溶液490gを得た。この溶液を50度Cまで冷却
し、粘度低下剤としてヘキシレングリコール5gおよび
イオン交換水2gを加えた。オクチル酸コバルト溶液の
コバルト含有量は、12.3%であり、溶液の粘度は3
35ポイズ(30度C)であった。しかしながら、一週
間、静置したところ二相に分離し、上層の粘度は6ポイ
ズで、下層の粘度は320ポイズとなった。
【0011】
【発明の効果】この発明のオクチル酸コバルト溶液から
なる印刷インキ用乾燥剤は、印刷用インキに混合するこ
とにより、相溶性が高く、臭気が無く、そのために作業
性に優れた印刷用インキを提供でき、また貯蔵した際
に、安定性の高い印刷インキ用乾燥剤となる。それは溶
剤を使用することがなく調整できるので、従来使用され
た溶剤としての揮発性有機化合物、とくに芳香族系化合
物を使用することが無いので、悪臭公害や、その廃棄に
伴う環境問題に配慮することを必要としない。なおこの
発明は、塗料などに使用した場合においても、同様の効
果を奏することができる。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a desiccant for printing ink comprising a cobalt soap solution, which has a high metal content and a viscosity equivalent to that of the printing ink. The present invention relates to a drying agent for printing ink having the same. [0002] Cobalt soap is used as an ink additive, a paint additive, a catalyst for synthesis, a plastic additive and the like, and exhibits an important function as a drying agent and a curing accelerator. However, cobalt soap having a high content of cobalt metal is in a solid state or has a high viscosity and poor fluidity. It is used with increased fluidity or increased fluidity using solvents such as toluene, xylene, or mineral oil. Furthermore, even if such a solvent is used, when it is difficult to increase the fluidity to a predetermined viscosity, the amount of the solvent may be increased,
Adjustment is made by adding a viscosity reducing agent. The use of these solvents and additives such as viscosity reducing agents is not preferred because it causes the physical properties of the printing ink to change. Also, with the recent spread of environmental problems, it is desired to suppress the use of solvents, especially volatile organic compounds. [0003] The present invention has a high compatibility by being mixed with a printing ink as a drying agent for the printing ink, and therefore has excellent workability and is stable when stored. It is an object of the present invention to obtain a desiccant for printing ink comprising a soluble cobalt soap solution. Means for Solving the Problems An organic carboxylic acid having 8 to 10 carbon atoms is added to cobalt octylate, and a cobalt octylate solution containing 10 to 14% of cobalt metal is heated to 30 ° C. C. A desiccant for printing ink, comprising a solution of cobalt octylate adjusted to a viscosity of 20 to 500 poise in C. DETAILED DESCRIPTION OF THE INVENTION The cobalt soap solution has a carbon number of 8 to 8.
Add 10 organic carboxylic acids. Particularly preferably, by adding octylic acid which is a reaction system drug,
A predetermined viscosity can be controlled without significantly lowering the metal content, and a product that becomes a drying agent for a printing ink with excellent storage stability can be obtained. As a result, the use of an aromatic compound as a solvent can be eliminated. As the aforementioned organic carboxylic acid,
Neodecanoic acid, octylic acid, caprylic acid, capric acid,
Nonanoic acid and secanoic acid. If the number of carbon atoms is 7 or less, the odor is strong and unsuitable. If the number of carbon atoms is 11 or more, it becomes a solid at normal temperature. Next, an example and a comparative example will be described. Example 1 317 g of octylic acid was weighed, placed in a 1 liter separable flask, and stirred with 130 parts of basic cobalt carbonate (cobalt content 45%).
g was added. In order to suppress the sudden generation of carbon dioxide,
The reaction temperature was gradually increased, and when the temperature reached 100 ° C., the increase in the reaction temperature was stopped, and the temperature was maintained for 1 hour while stirring was continued. Subsequently, in order to remove water generated during the reaction, the temperature was raised to 140 ° C., and the temperature was maintained for one hour while stirring was continued. Next, octylic acid 1
13 g was charged and cooled to 70 ° C. to obtain 480 g of a cobalt octylate solution. The cobalt content of the cobalt octylate solution is 12.3% and the viscosity of the solution is 2%.
It was 60 poise. One week later, when the viscosity of the solution was measured, it was 260 poise (30 ° C.), and there was no change. Example 2 317 g of octylic acid was weighed, placed in a 1-liter separable flask, and 160 g of a 25% aqueous sodium hydroxide solution was added with stirring to produce sodium octylate. Put this solution at 60 ° C
And 590 ml of an aqueous solution of cobalt sulfate adjusted to a cobalt concentration of 100 g / l was added over 30 minutes to produce cobalt octylate. The sodium sulfate by-produced at this time was removed by washing with water. Heating the obtained cobalt octylate solution to 140 ° C.,
The contained water was removed. Next, octylic acid 113
g, and 470 g of a cobalt octylate solution was obtained.
The cobalt content of the cobalt octylate solution is 12.4
% And the viscosity of the solution was 280 poise (30 ° C.). One week later, the viscosity of the solution was measured.
It was 80 poise (30 degrees C) and there was no change. Example 3 317 g of octylic acid was weighed and placed in a 1-liter separable flask, and 160 g of a 25% aqueous sodium hydroxide solution was added with stirring to produce sodium octylate. Put this solution at 60 ° C
And 590 ml of an aqueous solution of cobalt sulfate adjusted to a cobalt concentration of 100 g / l was added over 30 minutes to produce cobalt octylate. The sodium sulfate by-produced at this time was removed by washing with water. Heating the obtained cobalt octylate solution to 140 ° C.,
The contained water was removed. Next, octylic acid 143
g, and 500 g of a cobalt octylate solution was obtained.
The cobalt content of the cobalt octylate solution was 11.8.
% And the viscosity of the solution was 140 poise (30 ° C.). One week later, the viscosity of the solution was measured.
It was 40 poise (30 degrees C) and there was no change. Comparative Example 1: A decrease in viscosity was attempted using a petroleum-based solvent instead of octylic acid.
No fluid thing was obtained. That is, octylic acid 3
17 g is weighed, placed in a 1 liter separable flask, and stirred with a 25% aqueous sodium hydroxide solution 160
g was added to produce sodium octylate. To this solution was added 123 g of solvent aroma free solvent No. 6 (AF-6) manufactured by Nippon Oil Co., Ltd., and the mixture was maintained at 60 ° C.
590 ml of an aqueous solution of cobalt sulfate adjusted to a cobalt concentration of 100 g / liter was added over 30 minutes to produce cobalt octylate. The sodium sulfate by-produced at this time was removed by washing with water. The obtained cobalt octylate solution was heated to 140 ° C. to remove the contained water, thereby obtaining 490 g of a cobalt octylate solution. The cobalt content of the cobalt octylate solution is 1
Although it was 2.1%, the viscosity of the solution solidified when cooled to 30 ° C. Comparative Example 2: Under the conditions of Comparative Example 1, a small amount of a viscosity reducing agent was added. Although the viscosity immediately after the addition was low, phase separation occurred in about one week and was unstable with time. That is, 317 g of octylic acid was weighed, placed in a 1-liter separable flask, and 160 g of a 25% aqueous sodium hydroxide solution was added with stirring to produce sodium octylate. To this solution was added 123 g of Aroma Free Solvent No. 6 (AF-6) manufactured by Nippon Oil Co., Ltd.
590 ml of an aqueous solution of cobalt sulfate maintained at 0 ° C. and adjusted to a cobalt concentration of 100 g / l,
Added over minutes to produce cobalt octylate. The sodium sulfate by-produced at this time was removed by washing with water. The obtained cobalt octylate solution was heated to 140 ° C. to remove water contained therein, thereby obtaining 490 g of a cobalt octylate solution. The solution was cooled to 50 ° C., and 5 g of hexylene glycol and 2 g of ion-exchanged water were added as a viscosity reducing agent. The cobalt content of the cobalt octylate solution is 12.3% and the viscosity of the solution is 3%.
It was 35 poise (30 degrees C). However, upon standing for one week, the mixture separated into two phases, and the viscosity of the upper layer was 6 poise and the viscosity of the lower layer was 320 poise. The desiccant for printing ink comprising the cobalt octylate solution of the present invention, when mixed with the printing ink, has high compatibility, has no odor, and therefore has excellent workability. It can provide a printing ink, and becomes a highly stable drying ink for printing ink when stored. Since it can be adjusted without using a solvent, it does not use volatile organic compounds as solvents conventionally used, especially aromatic compounds, so that it takes into account odor pollution and environmental problems associated with its disposal. You don't need to. Note that the present invention can provide the same effect when used for paints and the like.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 武藤 秀樹 埼玉県草加市中根1丁目18番13号号日本化 学産業株式会社総合研究所内 (72)発明者 末永 和行 埼玉県草加市中根1丁目18番13号号日本化 学産業株式会社総合研究所内 (72)発明者 織田 二郎 埼玉県草加市中根1丁目18番13号号日本化 学産業株式会社総合研究所内 Fターム(参考) 4J039 BC27 EA12 ────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Hideki Muto 1-18-13, Nakane, Soka City, Saitama, Japan Gakkai Sangyo Co., Ltd. (72) Inventor Kazuyuki Suenaga 1-18-13, Nakane, Soka City, Saitama, Japan Gakkai Sangyo Co., Ltd. (72) Inventor Jiro Oda 1-18-13, Nakane, Soka City, Saitama, Japan Gakkai Sangyo Co., Ltd. F-term (reference) 4J039 BC27 EA12
Claims (1)
0の有機カルボン酸を添加し、コバルト金属が10〜1
4%含有したところのオクチル酸コバルト溶液を、30
度Cにおいて20〜500ポイズの粘度に調整したオク
チル酸コバルト溶液からなることを特徴とする印刷イン
キ用乾燥剤。Claims 1. A cobalt octylate having 8 to 1 carbon atoms.
0 organic carboxylic acid, and cobalt metal is 10 to 1
The cobalt octylate solution containing 4% was added to 30
A desiccant for printing ink, comprising a cobalt octylate solution adjusted to a viscosity of 20 to 500 poise at a degree C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001392830A JP3890372B2 (en) | 2001-11-19 | 2001-11-19 | Desiccant for printing ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001392830A JP3890372B2 (en) | 2001-11-19 | 2001-11-19 | Desiccant for printing ink |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2003155428A true JP2003155428A (en) | 2003-05-30 |
JP3890372B2 JP3890372B2 (en) | 2007-03-07 |
Family
ID=19188708
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001392830A Expired - Lifetime JP3890372B2 (en) | 2001-11-19 | 2001-11-19 | Desiccant for printing ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3890372B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008537970A (en) * | 2005-03-29 | 2008-10-02 | ジェネシス ツウ オブ エヌシイ,エルエルシイ | Drying accelerator and method of using the same |
-
2001
- 2001-11-19 JP JP2001392830A patent/JP3890372B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008537970A (en) * | 2005-03-29 | 2008-10-02 | ジェネシス ツウ オブ エヌシイ,エルエルシイ | Drying accelerator and method of using the same |
Also Published As
Publication number | Publication date |
---|---|
JP3890372B2 (en) | 2007-03-07 |
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