JPH086057B2 - Oil-based ink for inkjet recording - Google Patents
Oil-based ink for inkjet recordingInfo
- Publication number
- JPH086057B2 JPH086057B2 JP61194036A JP19403686A JPH086057B2 JP H086057 B2 JPH086057 B2 JP H086057B2 JP 61194036 A JP61194036 A JP 61194036A JP 19403686 A JP19403686 A JP 19403686A JP H086057 B2 JPH086057 B2 JP H086057B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- ink
- solvent
- based ink
- petroleum 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.)
- Expired - Lifetime
Links
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) この発明は、例えばインクジェット記録用油性インク
に関するものである。TECHNICAL FIELD The present invention relates to, for example, an oil-based ink for inkjet recording.
(従来の技術) インクジェット記録方式は記録ヘッドからインク液滴
を飛翔させて記録紙上にインク粒子を付着、浸透吸収さ
せて記録させる方式で、この方式による記録は低騒音で
あり、且つ記録の高速化及びカラー化が容易であり、ま
た普通紙が使用できる可能性があるため、近年各種プリ
ンター、ファクシミリ等への応用、開発が盛んに行なわ
れいる。(Prior Art) An inkjet recording method is a method in which ink droplets are ejected from a recording head to adhere and permeate and absorb ink particles on a recording paper, and recording is performed with low noise and high speed recording. Since it is easy to make color and color, and there is a possibility that plain paper can be used, application and development to various printers, facsimiles, etc. have been actively made in recent years.
これらインクジェット記録用インクとしては油性溶媒
に油性染料を溶解させた油性インク、或は水性溶媒に水
性染料を溶解させた水性インクが知られている。As these ink jet recording inks, an oil-based ink in which an oil-based dye is dissolved in an oil-based solvent, or an aqueous ink in which an aqueous dye is dissolved in an aqueous solvent is known.
(発明が解決しようとする問題点) このうち、油性インクは一般に、記録紙の選択範囲が
広く、速乾性(紙への浸透吸収性)、記録紙の耐水性が
良く、またノズルの目詰りを少なくなる等の利点を有す
ることが知られているが、上述のようなインクジェット
記録方式についてみればノズルで溶媒が蒸発し、染料が
ノズルで固化又は凝集し、インク液滴の吐出が行われな
くなるという問題点を抱えている。(Problems to be solved by the invention) Among them, the oil-based ink generally has a wide selection range of recording paper, quick drying (permeation and absorption into paper), good recording paper water resistance, and nozzle clogging. It is known to have the advantage of reducing the amount of ink, but in the ink jet recording method as described above, the solvent evaporates at the nozzle, the dye solidifies or aggregates at the nozzle, and ink droplets are ejected. It has the problem of disappearing.
また、この問題点を解決するため、油性インクの有機
溶媒として、一般に高沸点溶媒が用いられているが、こ
の高沸点溶媒は、油溶性染料の溶解能力が劣るため、染
料溶解濃度の影響で記録時の印字濃度が得られないので
画像品質が劣るという難点がある。Further, in order to solve this problem, as the organic solvent of the oil-based ink, a high-boiling point solvent is generally used, but this high-boiling point solvent is inferior in the dissolving ability of the oil-soluble dye, so that it is affected by the dye-dissolving concentration. Since the print density at the time of recording cannot be obtained, there is a problem that the image quality is inferior.
そこで、この発明は、ノズルの目詰りがなく、吐出安
定性の高い特にインクジェット記録方式に適した油性記
録インクを提供することを目的とするものである。Therefore, it is an object of the present invention to provide an oil-based recording ink that does not cause nozzle clogging and has high ejection stability, which is particularly suitable for an inkjet recording system.
(問題点を解決するための手段) 以上の問題点を解決するために、この発明ではパラフ
ィン系石油溶剤、芳香族系石油溶剤、ナフテン系石油溶
剤、オレフィン系石油溶剤、エステル類等の一種または
二種以上を組合せた有機溶剤に、油溶性染料を分散また
は溶解させてなるインクジェット記録用油性インクであ
って、下記一般式で表わされるポリオキシエチレンアル
キルアミン (式中Rは、炭素原子数6〜18のアルキル基、n,mは0
〜10の範囲である。) を0.5〜10Wt%含有することを特徴とするインクジェッ
ト記録用油性インクを提案するものである。(Means for Solving Problems) In order to solve the above problems, according to the present invention, one kind of paraffinic petroleum solvent, aromatic petroleum solvent, naphthene petroleum solvent, olefin petroleum solvent, esters and the like, or An oil-based ink for ink-jet recording, comprising an oil-soluble dye dispersed or dissolved in an organic solvent comprising a combination of two or more thereof, wherein the polyoxyethylene alkylamine is represented by the following general formula. (In the formula, R is an alkyl group having 6 to 18 carbon atoms, and n and m are 0.
It ranges from ~ 10. ) Is contained in an amount of 0.5 to 10 Wt%, and an oil-based ink for inkjet recording is proposed.
この発明に使用できる油溶性染料について特に限定さ
れないが、使用特性上記録画像の耐候性の良いものが望
ましく、例えば、 C.I.Solvent Black 3,7,22,34,50 C.I.Solvent Blue 14,25,35,48,108 C.I.Solvent Yellow 3,14,16,33,56 C.I.Solvent Red 18,24,27,122,135 等を挙げることができ、その添加量は添加後の溶解安定
性及びインクの物性値等を考慮して、20Wt%以下にする
ことが望ましい。The oil-soluble dye that can be used in the present invention is not particularly limited, but those having good weather resistance of the recorded image are desirable in terms of use characteristics, for example, CISolvent Black 3,7,22,34,50 CISolvent Blue 14,25,35,48,108. CISolvent Yellow 3,14,16,33,56 CISolvent Red 18,24,27,122,135 etc. can be mentioned, and the addition amount is 20 Wt% or less in consideration of the dissolution stability after addition and the physical properties of the ink. It is desirable to do.
また有機溶媒としてはインクの乾燥抑制のために蒸発
速度の遅い高沸点溶媒を用いることが望ましく、例え
ば、石油系溶剤としては、パラフィン系石油溶剤、芳香
族系石油溶剤、ナフテン系石油溶剤、オレフィン系石油
溶剤等の鉱物油を用いることができる。更に、安息香酸
エチル、安息香酸ブチル、酢酸2−エチルヘキシル、フ
タル酸ジブチル、アジピン酸プロピル、セバシン酸ジオ
クチル等のエステル類及びジブチルセロソルブ、フェニ
ルセロソルブ、ヘキシルセロソルブ、ブチルカルビトー
ル、ジブチルカルビトール、ジプロピレングリコールモ
ノメチルエーテル等のエーテル類等の一種または二種以
上を組合せて使用することができる。Further, as the organic solvent, it is desirable to use a high boiling point solvent having a slow evaporation rate in order to suppress the drying of the ink. For example, as the petroleum solvent, a paraffin petroleum solvent, an aromatic petroleum solvent, a naphthene petroleum solvent, an olefin are used. A mineral oil such as a petroleum solvent can be used. Further, esters such as ethyl benzoate, butyl benzoate, 2-ethylhexyl acetate, dibutyl phthalate, propyl adipate and dioctyl sebacate, and dibutyl cellosolve, phenyl cellosolve, hexyl cellosolve, butyl carbitol, dibutyl carbitol, dipropylene. One kind or two or more kinds of ethers such as glycol monomethyl ether can be used in combination.
更に、上記構造式で表わされるポリオキシエチレンア
ルキルアミンは本願発明者等の研究によれば弱カチオン
性ノニオン活性剤で、浸透性、湿潤性に優れ、且つ上記
有機溶剤に、油溶性染料を多量にしかも安定に溶解させ
る染料の溶解助剤として優れた性質を有している。Further, according to the study of the inventors of the present invention, the polyoxyethylene alkylamine represented by the above structural formula is a weak cationic nonionic activator, has excellent permeability and wettability, and contains a large amount of an oil-soluble dye in the organic solvent. In addition, it has excellent properties as a dissolution aid for a dye that can be stably dissolved.
なお、上記ポリオキシエチレンアルキルアミンの構造
式中、Rを炭素原子数6〜18のアルキル基としたのは、
この範囲外ではエチレンオキサイドの付加数に拘らず、
溶解助剤としての効果が劣る等の理由によるものであ
る。また、n,mを0〜10としたのは、10以上では油溶性
が損なわれるために染料の溶解性が不安定になる等の理
由によるものである。In the structural formula of the polyoxyethylene alkylamine, R is an alkyl group having 6 to 18 carbon atoms,
Outside this range, regardless of the number of ethylene oxide added,
This is because the effect as a dissolution aid is poor. The reason why n and m are set to 0 to 10 is that the solubility of the dye becomes unstable and the solubility of the dye becomes unstable at 10 or more.
また、ポリオキシエチレンアルキルアミンの添加量は
油溶性染料とその有機溶媒のインク組成に対して0.5Wt
%、特にインク物性値等を考慮すれば、0.5〜5Wt%の範
囲が好ましい。The amount of polyoxyethylene alkylamine added is 0.5 Wt with respect to the ink composition of the oil-soluble dye and its organic solvent.
%, Especially in consideration of ink physical properties and the like, the range of 0.5 to 5 Wt% is preferable.
(発明の効果) この発明に係るインクは、油溶性染料とその有機溶媒
に上記構造式で表わされるポリオキシエチレンアルキル
アミンを添加するものであるが、上述のようにポリオキ
シエチレンアルキルアミンは油溶性染料に対して優れた
溶解助剤としての特性があり、これを添加することによ
りインク成分中の油溶性染料が記録時に高印字濃度で、
しかも安定に有機溶媒に溶解される。(Effect of the Invention) The ink according to the present invention is one in which the polyoxyethylene alkylamine represented by the above structural formula is added to an oil-soluble dye and its organic solvent. There is a property as an excellent dissolution aid to the soluble dye, and by adding this, the oil-soluble dye in the ink component has a high printing density during recording,
Moreover, it is stably dissolved in the organic solvent.
したがって、この発明によればインクジェット記録用
油性インクとして十分な染料濃度が得られるので、印字
品の画像品質が優れたものとなる。Therefore, according to the present invention, a sufficient dye concentration can be obtained as an oil-based ink for inkjet recording, so that the image quality of a printed product is excellent.
また、この発明の油性インクはポリオキシエチレンア
ルキルアミンの添加により、有機溶媒の蒸発が減速され
る。これによりインクの乾燥、染料の凝集等が起こりに
くくなり、更にノズルの目詰り等がなく、吐出安定性も
高まる。Further, in the oil-based ink of the present invention, the addition of polyoxyethylene alkylamine slows down the evaporation of the organic solvent. As a result, drying of ink, aggregation of dye, etc. are less likely to occur, and further, nozzle clogging and the like are eliminated, and ejection stability is improved.
更に一般に溶解性が劣る溶媒は、低臭、低毒性のもの
が多いが、この発明では優れた溶解助剤特性を有するポ
リオキシエチレンアルキルアミンの添加により低溶解性
であるが低臭、低毒性の有機溶媒を使用することができ
る。Further, generally, solvents having poor solubility are often low in odor and low in toxicity, but in this invention, addition of polyoxyethylene alkylamine, which has excellent dissolution aid properties, results in low solubility but low odor and low toxicity. The organic solvent can be used.
また、この発明に係るインクは速乾性、耐水性に優れ
ているため、記録紙の選択範囲も広く、一般に市販され
ている普通紙にも使用することができる。Further, since the ink according to the present invention is excellent in quick-drying property and water resistance, the recording paper has a wide selection range and can be used for plain paper which is generally commercially available.
(実施例) 以下、この発明の実施例を示すが、この発明は勿論こ
れ等の実施例に限定されるものでない。(Examples) Examples of the present invention will be shown below, but the present invention is of course not limited to these examples.
配合例1 C.I.Solvent Black 3 10Wt% ポリオキシエチレンオレイルアミン(HLB=5) 5 〃
安息香酸ブチル 15 〃 EXXSOL D−100(エクソン化学社製) 70 〃 配合例2 C.I.Solvent Black 3 10Wt% ポリオキシエチレンオイルアミン(HLB=5) 5 〃 ハイソゾールSAS(日本石油社製) 15 〃 インクソルベント240(三菱石油社製) 70 〃 配合例3 C.I.Solvent Black 3 10Wt% ポリオキシエチレンステアリルアミン(HLB=7.5) 4
〃 安息香酸ブチル 15 〃 EXXSOL D−100 71 〃 配合例4 C.I.Solvent Black 3 10Wt% ポリオキシエチレンステアリルアミン(HLB=7.5) 5
〃 ハイソゾールSAS 15 〃 インクソルベント240 72 〃 比較配合例1 C.I.Solvent Black 3 5Wt% 安息香酸ブチル 25 〃 EXXSOL D−100 70 〃 比較配合例2 C.I.Solvent Black 3 5Wt% ハイソゾールSAS 25 〃 インクソルベント240 70 〃 上記の組成中、溶媒50Wt%除いた組成物をボールミル
で24時間以上混合し、それに溶媒50Wt%を加えて、その
上24時間以上ボールミルで混合した後、孔径1μ以下の
テフロン製フィルターで吸引濾過してインクを調整し、
溶解安定性試験を行なった。Formulation 1 CISolvent Black 3 10Wt% Polyoxyethylene oleylamine (HLB = 5) 5 〃
Butyl benzoate 15 〃 EXXSOL D-100 (manufactured by Exxon Chemical Co., Ltd.) 70 〃 Blending Example 2 CISolvent Black 3 10Wt% Polyoxyethylene oil amine (HLB = 5) 5 〃 Hisosol SAS (manufactured by Nippon Oil Co., Ltd.) 15 〃 Ink Solvent 240 (Manufactured by Mitsubishi Oil Co., Ltd.) 70 〃 Formulation 3 CISolvent Black 3 10Wt% Polyoxyethylene stearylamine (HLB = 7.5) 4
〃 Butyl benzoate 15 〃 EXXSOL D-100 71 〃 Formulation 4 CISolvent Black 3 10Wt% Polyoxyethylene stearylamine (HLB = 7.5) 5
〃 Hysol Zol SAS 15 〃 Ink Solvent 240 72 〃 Comparative Formulation Example 1 CISolvent Black 3 5Wt% Butyl Benzoate 25 〃 EXXSOL D-100 70 〃 Comparative Formulation Example 2 CISolvent Black 3 5Wt% Hysosol SAS 25 〃 Ink Solvent 240 70 〃 Above In the composition, the composition excluding 50 Wt% of the solvent was mixed in a ball mill for 24 hours or more, 50 Wt% of the solvent was added thereto, and the mixture was further mixed in the ball mill for 24 hours or more, and then suction-filtered with a Teflon filter having a pore size of 1 μm or less. Adjust the ink,
A dissolution stability test was performed.
(1)染料の溶解性試験 油溶性染料として、C.I.Solvent Black 3を選び、こ
れを各種有機溶剤、パラフィン系石油溶剤(EXXSOL D−
100)、芳香族石油溶剤(ハイソゾールSAS)、ナフテン
系石油溶剤(インソルベント240)、安息香酸ブチルに
それぞれ染料を1Wt%、5Wt%、10Wt%、15Wt%添加す
る。このとき溶解助剤であるポリオキシエチレンオレイ
ルアミン(HLB=5)を無添加、2.5Wt%、5Wt%、10Wt
%添加したもので染料の溶解性に差がでるか否かを調べ
た。(1) Dye solubility test CISolvent Black 3 was selected as an oil-soluble dye, and various organic solvents and paraffin petroleum solvents (EXXSOL D-
100), aromatic petroleum solvent (Hisosol SAS), naphthenic petroleum solvent (Insolvent 240), and butyl benzoate with 1Wt%, 5Wt%, 10Wt% and 15Wt% of dye, respectively. At this time, without adding polyoxyethylene oleylamine (HLB = 5) which is a dissolution aid, 2.5 Wt%, 5 Wt%, 10 Wt
%, It was investigated whether or not there was a difference in the solubility of the dyes.
評価は上記のように配合したものを、1昼夜常温で放
置した後、孔径1μのテフロン製フィルタで吸引濾過し
た時の残留物の有無を調べた。その結果を表1に示す。For the evaluation, after the mixture blended as described above was left at room temperature for one day, it was examined whether or not there was a residue when it was suction-filtered with a Teflon filter having a pore size of 1 μm. The results are shown in Table 1.
(2)保存安定性試験 上記実施例で得られたインクをガラス試験管に密封
し、−5℃および+60℃の条件下に1ヶ月放置した後、
孔径1μのテフロン製フィルターで吸引濾過し、残留物
の有無を調べた。その結果を表2に示す。(2) Storage stability test The inks obtained in the above examples were sealed in glass test tubes and allowed to stand under the conditions of -5 ° C and + 60 ° C for 1 month.
The mixture was suction-filtered with a Teflon filter having a pore size of 1 μm and examined for the presence of residues. The results are shown in Table 2.
Claims (1)
剤、ナフテン系石油溶剤、オレフィン系石油溶剤、エス
テル類等の一種または二種以上を組合せた有機溶剤に、
油溶性染料を分散または溶解させてなるインクジェット
記録用油性インクであって、下記一般式で表わされるポ
リオキシエチレンアルキルアミン (式中、Rは炭素原子数6〜18のアルキル基、n,mは0
〜10の範囲である。) を0.5〜10Wt%含有することを特徴とするインクジェッ
ト記録用油性インク。1. A paraffin-based petroleum solvent, an aromatic petroleum solvent, a naphthene-based petroleum solvent, an olefin-based petroleum solvent, an organic solvent in which one or more kinds thereof are combined,
An oil-based ink for ink-jet recording comprising an oil-soluble dye dispersed or dissolved therein, which is a polyoxyethylene alkylamine represented by the following general formula. (In the formula, R is an alkyl group having 6 to 18 carbon atoms, and n and m are 0.
It ranges from ~ 10. ) 0.5 to 10 Wt% is contained in the oil-based ink for inkjet recording.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61194036A JPH086057B2 (en) | 1986-08-21 | 1986-08-21 | Oil-based ink for inkjet recording |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61194036A JPH086057B2 (en) | 1986-08-21 | 1986-08-21 | Oil-based ink for inkjet recording |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6351483A JPS6351483A (en) | 1988-03-04 |
JPH086057B2 true JPH086057B2 (en) | 1996-01-24 |
Family
ID=16317868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61194036A Expired - Lifetime JPH086057B2 (en) | 1986-08-21 | 1986-08-21 | Oil-based ink for inkjet recording |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH086057B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007108382A1 (en) | 2006-03-17 | 2007-09-27 | Hitachi Maxell, Ltd. | Oil-based ink composition |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4234835B2 (en) * | 1999-02-17 | 2009-03-04 | シヤチハタ株式会社 | Oil-based ink |
CN1196753C (en) * | 1999-05-20 | 2005-04-13 | 阪田油墨株式会社 | Oil-based ink for ink-jet recording |
JP4330260B2 (en) * | 2000-08-31 | 2009-09-16 | サカタインクス株式会社 | Oil-based inkjet recording ink |
JP2018001479A (en) * | 2016-06-29 | 2018-01-11 | セイコーエプソン株式会社 | Droplet discharge method |
US20230031477A1 (en) * | 2019-12-20 | 2023-02-02 | Kao Corporation | Inkjet inks |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5790067A (en) * | 1980-11-25 | 1982-06-04 | Canon Inc | Recording liquid |
JPS58213068A (en) * | 1982-06-03 | 1983-12-10 | Canon Inc | Recording liquid |
-
1986
- 1986-08-21 JP JP61194036A patent/JPH086057B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007108382A1 (en) | 2006-03-17 | 2007-09-27 | Hitachi Maxell, Ltd. | Oil-based ink composition |
EP2508576A2 (en) | 2006-03-17 | 2012-10-10 | Hitachi Maxell, Ltd. | Oil-based ink composition |
US9428660B2 (en) | 2006-03-17 | 2016-08-30 | Hitachi Maxell, Ltd. | Oil-based ink composition |
Also Published As
Publication number | Publication date |
---|---|
JPS6351483A (en) | 1988-03-04 |
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