JPH05112745A - Ink solvent - Google Patents
Ink solventInfo
- Publication number
- JPH05112745A JPH05112745A JP30230391A JP30230391A JPH05112745A JP H05112745 A JPH05112745 A JP H05112745A JP 30230391 A JP30230391 A JP 30230391A JP 30230391 A JP30230391 A JP 30230391A JP H05112745 A JPH05112745 A JP H05112745A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- fatty acid
- ink
- solvent
- ester
- 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
【0001】[0001]
【産業上の利用分野】本発明は、インキ用溶剤、特にイ
ンキ用高沸点溶剤に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a solvent for ink, especially a high boiling point solvent for ink.
【0002】[0002]
【従来の技術】従来、インキに用いられていた溶剤は、
石油系の炭化水素,IPA等のアルコール,グリコール
化合物,ケトン類,酢酸エステルがある。中でも、沸点
200℃以上の高沸点溶剤に用いられる溶剤は、石油系
の炭化水素が主体であった。石油系炭化水素以外の高沸
点溶剤としては、トリデカノール,ジエチレングリコー
ル,トリエチレングリコール,ジプロピレングリコー
ル,グリセリン,ジエチレングリコールモノブチルエー
テル,ジエチレングリコールモノエチルエーテルアセテ
ート,ジエチレングリコールモノブチルエーテルアセテ
ートがある。2. Description of the Related Art Solvents conventionally used for ink are
There are petroleum hydrocarbons, alcohols such as IPA, glycol compounds, ketones, and acetic acid esters. Among them, the solvent used for the high boiling point solvent having a boiling point of 200 ° C. or higher was mainly petroleum hydrocarbons. High-boiling solvents other than petroleum hydrocarbons include tridecanol, diethylene glycol, triethylene glycol, dipropylene glycol, glycerin, diethylene glycol monobutyl ether, diethylene glycol monoethyl ether acetate, and diethylene glycol monobutyl ether acetate.
【0003】[0003]
【発明が解決しようとする課題】近年、インキ取扱者の
健康に対する配慮や残存するインキの溶剤成分による印
刷物の安全性の観点から、これらの溶剤を減らし、安全
性を高めたいという要望がある。これらの溶剤を減ら
し、安全性を高める方法としては、インキのビヒクル構
成成分であるアマニ油等の動植物油脂の含量を高め、溶
剤の使用比率を低減する方法がある。しかしながら、イ
ンキ中の動植物油脂成分を高めると、インキの粘度が著
しく上昇してしまう。従って、動植物油脂の比率を高め
たインキは、従来のインキより流動性がなく、使用性が
悪い。また、特に浸透乾燥が要求されるインキは、ビヒ
クルの粘度が高いと浸透速度が遅く、乾燥性が悪くな
る。従来の技術で、これらの問題を解決するには、石油
系等の従来使用されていた溶剤もある程度使わざるを得
ないことになってしまう。In recent years, from the viewpoints of the health of the ink handler and the safety of the printed matter due to the residual solvent component of the ink, there is a demand to reduce the amount of these solvents and enhance the safety. As a method of reducing the amount of these solvents to enhance the safety, there is a method of increasing the content of animal and vegetable oils and fats such as linseed oil, which is a vehicle constituent of the ink, and reducing the use ratio of the solvent. However, if the content of animal and vegetable oils and fats in the ink is increased, the viscosity of the ink will remarkably increase. Therefore, an ink having a high proportion of animal and vegetable oils and fats has less fluidity than conventional inks and is inferior in usability. In addition, in the case of inks that are particularly required to be permeated and dried, if the viscosity of the vehicle is high, the permeation rate is slow and the drying properties are poor. In order to solve these problems by the conventional technique, it is necessary to use a solvent such as a petroleum-based solvent which has been conventionally used to some extent.
【0004】本発明の目的は、このような状況に鑑み、
従来の石油系溶剤を用いずに、安全性が高く、従来のイ
ンキの性能を損なわないインキ用溶剤を得ることにあ
る。In view of such a situation, an object of the present invention is to
Another object of the present invention is to obtain an ink solvent that is highly safe and does not impair the performance of conventional inks without using conventional petroleum-based solvents.
【0005】[0005]
【課題を解決するための手段】本発明者は、鋭意研究の
結果、以下の脂肪酸モノエステルが、この目的に合致す
ることを見いだし、本発明を完成した。即ち本発明は、
下記の一般式化1で示される脂肪酸モノエステルを主成
分とするインキ用溶剤である。As a result of earnest research, the present inventor has found that the following fatty acid monoesters meet this purpose, and completed the present invention. That is, the present invention is
It is an ink solvent containing a fatty acid monoester represented by the following general formula 1 as a main component.
【0006】[0006]
【化1】 [Chemical 1]
【0007】本発明における脂肪酸モノエステルを構成
する脂肪酸は、アルキル残基の炭素数5〜21、即ち、
カプロン酸,カプリル酸,カプリン酸,イソオクタン
酸,イソノナン酸,ラウリン酸,ミリスチン酸,パルミ
チン酸,パルミトオレイン酸,ステアリン酸,イソステ
アリン酸,ヒドロキシステアリン酸,オレイン酸,リノ
ール酸,リシノール酸,リノレイン酸,エレオステアリ
ン酸,アラキジン酸,アラキドン酸,ベヘン酸,エルカ
酸等である。これらの脂肪酸は、混合物で充分で、実用
上も価格の安い混合物が望ましい。また、これらの脂肪
酸は、主に動植物油脂由来であり、実際上は、ヤシ油脂
肪酸,パーム油脂肪酸,ナタネ油脂肪酸,大豆油脂肪
酸,水添大豆油脂肪酸,アマニ油脂肪酸,桐油脂肪酸,
トール油脂肪酸,牛脂脂肪酸,魚油脂肪酸,ダイマー酸
等、あるいは、その蒸留等による分別脂肪酸が使用可能
である。The fatty acid constituting the fatty acid monoester in the present invention has 5 to 21 carbon atoms in the alkyl residue, that is,
Caproic acid, caprylic acid, capric acid, isooctanoic acid, isononanoic acid, lauric acid, myristic acid, palmitic acid, palmitooleic acid, stearic acid, isostearic acid, hydroxystearic acid, oleic acid, linoleic acid, ricinoleic acid, linoleic acid , Eleostearic acid, arachidic acid, arachidonic acid, behenic acid, erucic acid and the like. A mixture of these fatty acids is sufficient, and a mixture that is inexpensive in practical use is desirable. Further, these fatty acids are mainly derived from animal and vegetable oils and fats, and in practice, coconut oil fatty acid, palm oil fatty acid, rapeseed oil fatty acid, soybean oil fatty acid, hydrogenated soybean oil fatty acid, linseed oil fatty acid, tung oil fatty acid,
Tall oil fatty acid, beef tallow fatty acid, fish oil fatty acid, dimer acid, etc., or fractionated fatty acid obtained by distillation thereof can be used.
【0008】本発明における脂肪酸モノエステルを構成
するアルコールは、アルキル基の炭素数1〜4、即ち、
メタノール,エタノール,プロパノール,イソプロパノ
ール,ブタノール,イソブチルアルコール等である。The alcohol constituting the fatty acid monoester in the present invention has 1 to 4 carbon atoms in the alkyl group, that is,
Examples include methanol, ethanol, propanol, isopropanol, butanol and isobutyl alcohol.
【0009】エステル化は、油脂からのアルコリシス、
あるいは脂肪酸の直接エステル化を常法で行うことによ
り、容易に得られる。得られたエステルは、蒸留,脱
色,脱臭等の精製を行っても良い。Esterification is an alcoholysis from fats and oils,
Alternatively, it can be easily obtained by directly esterifying a fatty acid by a conventional method. The obtained ester may be purified by distillation, decolorization, deodorization and the like.
【0010】本発明のエステルの沸点は、最も低いカプ
ロン酸メチルで約206℃、その後炭素数の増加に伴い
沸点も上昇する。粘度についても同様な傾向にあり、イ
ンキの用途に合わせてエステルの組成を選択できる。本
発明のエステルは、いずれもインキの樹脂成分であるロ
ジン,フェノール樹脂,石油樹脂等を充分に溶解する。
インキの粘度,溶剤の沸点については、エステルのアル
キル基組成を変えることにより、コントロール可能であ
る。従って、従来の石油系高沸点溶剤を充分に置き換え
ることが可能である。本発明のエステルは、エステル結
合が生態系で容易に分解され、分解物である脂肪酸とア
ルコールもその由来から安全性が高いという利点があ
る。以上の様に、本発明のインキ用溶剤を用いたインキ
は、特に、高沸点溶剤を用い、浸透乾燥が要求される新
聞インキ等の平版インキ、あるいは凸版インキに安全性
の高い溶剤として使用可能である。The boiling point of the ester of the present invention is about 206 ° C. with the lowest methyl caproate, and then the boiling point rises as the carbon number increases. The viscosity has a similar tendency, and the composition of the ester can be selected according to the use of the ink. Each of the esters of the present invention sufficiently dissolves rosin, phenol resin, petroleum resin, etc., which are resin components of ink.
The viscosity of the ink and the boiling point of the solvent can be controlled by changing the alkyl group composition of the ester. Therefore, it is possible to sufficiently replace the conventional petroleum-based high boiling point solvent. The ester of the present invention has an advantage that the ester bond is easily decomposed in the ecosystem, and the decomposed products, fatty acid and alcohol, are highly safe because of their origin. As described above, the ink using the ink solvent of the present invention can be used as a highly safe solvent for lithographic inks such as newspaper inks, which require permeation drying, or for letterpress inks, especially using high boiling point solvents. Is.
【0011】[0011]
実施例1 大豆油を、メタノールでアルコリシスし、大豆脂肪酸メ
チルエステルを得た。このエステルの沸点は、300℃
以上であった。大豆脂肪酸メチルエステル30部,アマ
ニ油30部,ロジン40部を、窒素気流下、180℃で
加熱攪拌した結果、均一に溶解した。このビヒクルの粘
度は、40Stであった。Example 1 Soybean oil was subjected to alcoholysis with methanol to obtain soybean fatty acid methyl ester. The boiling point of this ester is 300 ℃
That was all. 30 parts of soybean fatty acid methyl ester, 30 parts of linseed oil, and 40 parts of rosin were heated and stirred at 180 ° C. under a nitrogen stream, and as a result, they were uniformly dissolved. The viscosity of this vehicle was 40St.
【0012】実施例2 ヤシ油脂肪酸を蒸留して得たカプリル酸を、メタノール
で直接エステル化し、カプリル酸メチルエステルを得
た。このエステルの沸点は、230〜250℃であっ
た。カプリル酸メチルエステル30部,アマニ油30
部,ロジン変性フェノール樹脂40部を、窒素気流下、
180℃で加熱攪拌した結果、均一に溶解した。このビ
ヒクルの粘度は、10Stであった。Example 2 Caprylic acid obtained by distilling coconut oil fatty acid was directly esterified with methanol to obtain caprylic acid methyl ester. The boiling point of this ester was 230 to 250 ° C. Caprylic acid methyl ester 30 parts, linseed oil 30
Part, 40 parts of rosin-modified phenolic resin, under a nitrogen stream,
As a result of heating and stirring at 180 ° C., it was uniformly dissolved. The viscosity of this vehicle was 10St.
【0013】実施例3 牛脂ダイマー酸を蒸留して得たイソステアリン酸を、イ
ソブチルアルコールと直接エステル化し、イソステアリ
ン酸イソブチルエステルを得た。このエステルの沸点
は、300℃以上であった。イソステアリン酸イソブチ
ルエステル30部,アマニ油30部,ロジン変性フェノ
ール樹脂40部を、窒素気流下、180℃で加熱攪拌し
た結果、均一に溶解した。このビヒクルの粘度は、10
0Stであった。Example 3 Isostearic acid obtained by distilling beef tallow dimer acid was directly esterified with isobutyl alcohol to obtain isostearic acid isobutyl ester. The boiling point of this ester was 300 ° C. or higher. 30 parts of isostearic acid isobutyl ester, 30 parts of linseed oil, and 40 parts of rosin-modified phenol resin were heated and stirred at 180 ° C. under a nitrogen stream, and as a result, they were uniformly dissolved. The viscosity of this vehicle is 10
It was 0St.
【0014】実施例4 実施例1,2,3および比較例1のそれぞれのビヒクル
80部に、カーボンブラック20部を練り込み、インキ
様のペーストを作成した。このペーストを新聞紙に薄く
塗布し、一昼夜放置した結果、いずれも同様な乾燥状態
が得られた。Example 4 20 parts of carbon black was kneaded into 80 parts of each vehicle of Examples 1, 2, 3 and Comparative Example 1 to prepare an ink-like paste. As a result of applying this paste thinly to a newspaper and leaving it for one day and night, the same dried state was obtained.
【0015】比較例1 通常使用されているインキ組成物を、比較のため調合し
た。高沸点石油系溶剤(沸点:290〜310℃)30
部,アマニ油30部,ロジン変性フェノール樹脂40部
を、窒素気流下、180℃で加熱溶解した。このビヒク
ルの粘度は、80Stであった。Comparative Example 1 A commonly used ink composition was formulated for comparison. High boiling point petroleum solvent (boiling point: 290-310 ° C) 30
Parts, 30 parts of linseed oil, and 40 parts of rosin-modified phenol resin were heated and dissolved at 180 ° C. under a nitrogen stream. The viscosity of this vehicle was 80St.
【0016】[0016]
【発明の効果】実施例に示したように、本発明のエステ
ルを溶剤として用いたビヒクルは、高沸点石油系溶剤を
使用したビヒクルと同様に、インキの皮膜形成物質であ
る樹脂と乾性油(アマニ油)を適切な粘度で含有したも
のであり、このビヒクルを用いたインキは、従来品とほ
ぼ同等の性能を有している。本発明のエステルは、動植
物油脂由来として存在する脂肪酸を使用しているため、
石油系溶剤に較べ安全性が高い。また、動植物油脂は再
生産可能な資源であり、この点からも本発明は産業上の
優位性がある。As shown in the examples, the vehicle using the ester of the present invention as a solvent is similar to the vehicle using a high boiling point petroleum solvent, and the resin and the drying oil ( Linseed oil) is contained at an appropriate viscosity, and the ink using this vehicle has almost the same performance as conventional products. The ester of the present invention uses a fatty acid that is derived from animal and vegetable fats and oils,
Higher safety than petroleum solvent. In addition, animal and vegetable fats and oils are reproducible resources, and the present invention is industrially superior also in this respect.
Claims (2)
エステルを主成分とするインキ用溶剤。 【化1】 1. An ink solvent containing a fatty acid monoester represented by the following general formula 1 as a main component. [Chemical 1]
脂肪酸のアルキル残基である請求項1記載のインキ用溶
剤。2. The ink solvent according to claim 1, wherein R 1 in the general formula 1 is an alkyl residue of a fatty acid derived from animal and vegetable oils and fats.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30230391A JP3317512B2 (en) | 1991-10-22 | 1991-10-22 | Solvent for ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30230391A JP3317512B2 (en) | 1991-10-22 | 1991-10-22 | Solvent for ink |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05112745A true JPH05112745A (en) | 1993-05-07 |
JP3317512B2 JP3317512B2 (en) | 2002-08-26 |
Family
ID=17907351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30230391A Expired - Lifetime JP3317512B2 (en) | 1991-10-22 | 1991-10-22 | Solvent for ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3317512B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001098197A (en) * | 1999-09-30 | 2001-04-10 | Toshiba Corp | Recording liquid and recording device |
WO2002020679A1 (en) * | 2000-09-08 | 2002-03-14 | Sakata Inx Corp. | Ink composition for offset printing |
JP2003073581A (en) * | 2001-08-31 | 2003-03-12 | Dainippon Ink & Chem Inc | Base composition for pigment dispersion and dispersing method |
JP2004346135A (en) * | 2003-05-20 | 2004-12-09 | Tohoku Ricoh Co Ltd | W/o type emulsion ink for stencil printing |
EP1520886A1 (en) * | 2003-10-01 | 2005-04-06 | Cognis Deutschland GmbH & Co. KG | Use of fatty acid esters based on branched fatty acids as solvents for printing inks |
JP2005132907A (en) * | 2003-10-29 | 2005-05-26 | The Inctec Inc | Oily ink for inkjet recording |
JP2007154149A (en) * | 2005-12-08 | 2007-06-21 | Toshiba Tec Corp | Non-aqueous ink composition for ink jet |
-
1991
- 1991-10-22 JP JP30230391A patent/JP3317512B2/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001098197A (en) * | 1999-09-30 | 2001-04-10 | Toshiba Corp | Recording liquid and recording device |
WO2002020679A1 (en) * | 2000-09-08 | 2002-03-14 | Sakata Inx Corp. | Ink composition for offset printing |
JP2003073581A (en) * | 2001-08-31 | 2003-03-12 | Dainippon Ink & Chem Inc | Base composition for pigment dispersion and dispersing method |
JP4556091B2 (en) * | 2001-08-31 | 2010-10-06 | Dic株式会社 | Base composition for dispersion of pigment and dispersion method |
JP2004346135A (en) * | 2003-05-20 | 2004-12-09 | Tohoku Ricoh Co Ltd | W/o type emulsion ink for stencil printing |
JP4510404B2 (en) * | 2003-05-20 | 2010-07-21 | 東北リコー株式会社 | W / O emulsion ink for stencil printing |
EP1520886A1 (en) * | 2003-10-01 | 2005-04-06 | Cognis Deutschland GmbH & Co. KG | Use of fatty acid esters based on branched fatty acids as solvents for printing inks |
JP2005132907A (en) * | 2003-10-29 | 2005-05-26 | The Inctec Inc | Oily ink for inkjet recording |
JP4537036B2 (en) * | 2003-10-29 | 2010-09-01 | 株式会社Dnpファインケミカル | Oil-based ink for inkjet recording |
JP2007154149A (en) * | 2005-12-08 | 2007-06-21 | Toshiba Tec Corp | Non-aqueous ink composition for ink jet |
Also Published As
Publication number | Publication date |
---|---|
JP3317512B2 (en) | 2002-08-26 |
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