JPH086060B2 - Ink solvent - Google Patents
Ink solventInfo
- Publication number
- JPH086060B2 JPH086060B2 JP62146240A JP14624087A JPH086060B2 JP H086060 B2 JPH086060 B2 JP H086060B2 JP 62146240 A JP62146240 A JP 62146240A JP 14624087 A JP14624087 A JP 14624087A JP H086060 B2 JPH086060 B2 JP H086060B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- solvent
- petroleum hydrocarbon
- weight
- parts
- 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〕 本発明はインキ用溶剤に関し、詳しくはインキに適正
な流動性(レオロジー特性)を付与するとともに、乾燥
性に優れたインキ用溶剤に関する。TECHNICAL FIELD The present invention relates to an ink solvent, and more particularly to an ink solvent that imparts proper fluidity (rheological properties) to ink and is excellent in drying property.
一般に、高速印刷及び大量印刷に使用されるインキに
は、高度の印刷適性と作業適性が要求されている。これ
らの適性は、顔料,ビヒクル(樹脂,溶剤),助剤を組
み合わせてインキに一定のレオロジー特性を付与するこ
とにより達成されることが知られている。In general, inks used for high-speed printing and high-volume printing are required to have high printability and workability. It is known that these suitability is achieved by combining pigments, vehicles (resins, solvents), and auxiliaries to impart certain rheological properties to the ink.
ところで、従来からインキのレオロジー特性とインキ
の構成物質組成との関係については、各種の研究がなさ
れている。しかしながら、このレオロジー特性とインキ
の重要な構成物質の一つであるビヒクル、特に溶剤との
関係については未だ充分な検討がなされていないのが現
状であり、また今までのところ、高速・大量印刷技術の
進歩に応じた高性能(適正な流動性,乾燥性,耐ミスチ
ング性など)のインキは開発されていない。By the way, conventionally, various studies have been conducted on the relationship between the rheological properties of ink and the composition of constituent substances of ink. However, the relationship between this rheological property and the vehicle that is one of the important constituents of the ink, especially the solvent, has not yet been fully investigated, and so far, high-speed, large-volume printing has not been performed. Ink with high performance (proper fluidity, drying property, misting resistance, etc.) has not been developed in response to technological advances.
本発明者らは、上述したような高性能のインキを開発
することを目的として、様々な検討を重ね、特にインキ
のレオロジー特性とインキ溶剤、とりわけ石油系溶剤と
の関係に着目して、様々な角度から研究を続けた。The inventors of the present invention have conducted various studies for the purpose of developing a high-performance ink as described above, paying particular attention to the relationship between the rheological properties of the ink and the ink solvent, especially the petroleum solvent, I continued my research from various angles.
その結果、ナフテン分含量が30%以上と多く、しかも
芳香族分含量が2%以下と少ないものであって、そのう
え適当な動粘度,粘度指数,流動点を有する石油系炭化
水素溶剤が、高性能インキの製造を可能にするものであ
ることを見出した。本発明はかかる知見に基いて完成し
たものである。As a result, the naphthene content is as high as 30% or more, the aromatic content is as low as 2% or less, and the petroleum hydrocarbon solvent having an appropriate kinematic viscosity, viscosity index and pour point is high. It has been found that it enables the production of high performance inks. The present invention has been completed based on such findings.
すなわち本発明は、40℃における動粘度0.5〜500cSt,
粘度指数60以上,ナフテン分含量30%以上,芳香族分含
量2%以下および流動点−20℃以下である石油系炭化水
素からなるインキ用溶剤を提供するものである。That is, the present invention, the kinematic viscosity at 40 ℃ 0.5 ~ 500cSt,
It is intended to provide an ink solvent comprising a petroleum hydrocarbon having a viscosity index of 60 or more, a naphthene content of 30% or more, an aromatic content of 2% or less and a pour point of -20 ° C or less.
本発明のインキ用溶剤である石油系炭化水素は、まず
40℃における動粘度が0.5〜500cSt、好ましくは2〜200
cStである。ここで、動粘度が0.5cSt未満では、蒸発性
が高く、印刷機上での安定性が悪いという問題が生じ、
一方500cstを越えると、乾燥性の低下が著しくなり好ま
しくない。The petroleum hydrocarbon that is the solvent for the ink of the present invention is
Kinematic viscosity at 40 ° C is 0.5 to 500 cSt, preferably 2 to 200
cSt. Here, when the kinematic viscosity is less than 0.5 cSt, there is a problem that the evaporation property is high and the stability on the printing press is poor,
On the other hand, when it exceeds 500 cst, the drying property remarkably decreases, which is not preferable.
また上記石油系炭化水素は、粘度指数が60以上、好ま
しくは70以上である。粘度指数が60未満では、樹脂が膨
潤しすぎて乾燥性で低下するという問題がある。The petroleum hydrocarbon has a viscosity index of 60 or more, preferably 70 or more. When the viscosity index is less than 60, there is a problem that the resin is excessively swelled and the drying property is deteriorated.
さらにこの石油系炭化水素は、ナフテン分含量(%
CN)が30%以上、好ましくは30〜50%のものである。こ
のナフテン分含量が30%未満では、インキのビヒクルで
ある樹脂や顔料との相溶性が悪くなり、本発明の目的を
達成することができない。Furthermore, this petroleum hydrocarbon has a naphthene content (%
C N ) is 30% or more, preferably 30 to 50%. If the naphthene content is less than 30%, the compatibility with the resin or pigment that is the vehicle of the ink becomes poor, and the object of the present invention cannot be achieved.
上記石油系炭化水素の芳香族分含量(%CA)について
は、2%以下でなければならず、好ましくは1%以下で
ある。この芳香族分含量が2%を越えるものでは、溶剤
の外観が悪化し、また安全性の上でも好ましくない。The aromatic content (% C A ) of the petroleum hydrocarbon must be 2% or less, preferably 1% or less. If the aromatic content exceeds 2%, the appearance of the solvent is deteriorated and it is not preferable in terms of safety.
なお、上述のナフテン分含量(%CN)および芳香族分
含量(%CA)は、n−d−M法による環分析値である。The above-mentioned naphthene content (% C N ) and aromatic content (% C A ) are ring analysis values by the ndM method.
また、この石油系炭化水素は、流動点が−20℃以下、
好ましくは−30%以下のものである。流動点が−20℃を
越えるものでは、冬期又は寒冷地で使用する際に、取扱
い性及び圧送性が低下するという問題があり不適当であ
る。Further, this petroleum hydrocarbon has a pour point of -20 ° C or lower,
It is preferably -30% or less. If the pour point exceeds -20 ° C, there is a problem that the handling property and the pumping property are deteriorated when it is used in winter or in a cold region, which is unsuitable.
本発明のインキ用溶剤である石油系炭化水素は、叙上
の如き性状を有するものであればよいが、そのほか全酸
価が0.1mgKOH/g以下であることが、一層好ましい条件で
ある。The petroleum hydrocarbon as the solvent for the ink of the present invention may have any of the above properties, but it is more preferable that the total acid value is 0.1 mgKOH / g or less.
このような石油系炭化水素は、各種の方法により製造
することができる。例えばパラフィン基系原油,中間基
系原油あるいはナフテン基系原油を、常圧蒸留した残渣
をさらに減圧蒸留して得られる留出油を所望により溶剤
脱ロウし、さらに二段水素化処理したものを水素化脱ロ
ウし、引き続いて必要に応じて精密蒸留すれば、所定の
性状の石油系炭化水素を得ることができる。Such petroleum hydrocarbons can be produced by various methods. For example, distillate obtained by subjecting paraffin-based crude oil, intermediate-based crude oil, or naphthene-based crude oil to atmospheric distillation to obtain a distillate obtained by further distilling under reduced pressure may be subjected to solvent dewaxing and further subjected to a two-stage hydrotreatment. By subjecting to hydrodewaxing and subsequent precision distillation if necessary, a petroleum hydrocarbon having a predetermined property can be obtained.
本発明では、上記の石油系炭化水素をインキの溶剤と
して用いるが、この溶剤を使用してインキを製造するに
あたっては、従来から知られている公知の方法によれば
よい。つまり、本発明の溶剤と樹脂を加えたビヒクルに
適当な顔料を加え、さらに必要に応じて助剤(湿潤剤,
展色剤など)を加えたものを充分に練肉してカラーベー
スを作る。これにさらに本発明の溶剤を加えて希釈して
インキとすればよい。In the present invention, the above-mentioned petroleum hydrocarbon is used as a solvent for the ink, and the ink may be produced using this solvent by any known method known in the art. That is, a suitable pigment is added to the vehicle of the present invention containing a solvent and a resin, and if necessary, an auxiliary agent (wetting agent,
Make a color base by thoroughly kneading the mixture with a color-developing agent). The solvent of the present invention may be further added to this to dilute it into an ink.
ここで用いる顔料は、所望するインキの色などにより
様々であるが、従来から広く用いられているものを充当
すればよく、例えばカーボンブラック,ジスアゾイエロ
ー,カーミン6B,フタロシアニンブルーなどがあげられ
る。The pigment used here varies depending on the desired color of the ink and the like, but those conventionally used widely can be used, and examples thereof include carbon black, disazo yellow, carmine 6B, and phthalocyanine blue.
また、ビヒクルとして加える樹脂には、天然および合
成樹脂があるが、具体的には石油樹脂,ロジン変性フェ
ノール樹脂,アルキッド樹脂,重合アマニ油などがあげ
られる。The resin added as a vehicle includes natural and synthetic resins, and specific examples thereof include petroleum resin, rosin-modified phenol resin, alkyd resin and polymerized linseed oil.
さらに、湿潤剤として脂肪酸アミン,エステル化脂肪
酸などがあげられ、展色剤として天然ワックス,合成ワ
ックス,粘土,炭酸カルシウムなどがあげられる。Furthermore, fatty acid amines, esterified fatty acids and the like can be used as wetting agents, and natural wax, synthetic wax, clay, calcium carbonate and the like can be used as color developing agents.
次に、本発明を実施例および比較例によりさらに詳し
く説明する。Next, the present invention will be described in more detail with reference to Examples and Comparative Examples.
実施例1(藍色インキの調製) 中間基系原油を常圧蒸留及び減圧蒸留して得られた留
出油を、二段水添処理し、さらに水添脱ロウ処理して得
られた石油系炭化水素溶剤(40℃における動粘度96cSt,
粘度指数85,流動点−45℃,%CA0.2,%CN32.0)を用い
て次の如く藍色インキを調製した。Example 1 (Preparation of indigo color ink) Petroleum carbonization obtained by subjecting a distillate obtained by distilling an intermediate base crude oil to atmospheric distillation and vacuum distillation to a two-stage hydrogenation treatment and further hydrodewaxing treatment. Hydrogen solvent (kinematic viscosity at 40 ℃ 96cSt,
A cyan ink was prepared as follows using a viscosity index of 85, pour point of −45 ° C.,% C A 0.2,% C N 32.0).
すなわち、まず上記石油系炭化水素溶剤70重量部,フ
タロシアニンブルー30重量部および標準インキ添加剤10
重量部とを充分に練り合わせてカラーベースを作り、続
いてこのカラーベース24重量部を上記石油系炭化水素溶
剤70重量部に加え希釈して藍色インキを調製した。That is, first, 70 parts by weight of the above petroleum hydrocarbon solvent, 30 parts by weight of phthalocyanine blue, and 10 parts by weight of the standard ink additive.
A color base was prepared by thoroughly kneading with 20 parts by weight of the color base, and subsequently 24 parts by weight of the color base was added to 70 parts by weight of the petroleum hydrocarbon solvent to dilute the color base ink.
比較例1(藍色インキの調製) ナフテン基系原油を常圧蒸留及び減圧蒸留して得られ
た留出油を、溶剤抽出処理して得られた石油系炭化水素
溶剤(40℃における動粘度102cSt,粘度指数42,流動点−
20℃,%CA6.0,%CN39.5)を用いたこと以外は、実施例
1と同様にして藍色インキを調製した。Comparative Example 1 (Preparation of Indigo Color Ink) Petroleum hydrocarbon solvent obtained by subjecting a distillate oil obtained by subjecting a naphthene-based crude oil to atmospheric distillation and vacuum distillation to a solvent extraction treatment (kinematic viscosity at 40 ° C) 102cSt, viscosity index 42, pour point −
A cyan ink was prepared in the same manner as in Example 1 except that 20 ° C.,% C A 6.0,% C N 39.5) was used.
実施例2(黄色インキの調製) 上記実施例1で得られた石油系炭化水素溶剤73重量
部,ジスアゾイエロー30重量部および標準インキ添加剤
10重量部とを充分に練り合わせてカラーベースを作り、
続いてこのカラーベース140重量部を上記石油系炭化水
素溶剤95重量部に加え希釈して藍色インキを調製した。Example 2 (Preparation of Yellow Ink) 73 parts by weight of the petroleum hydrocarbon solvent obtained in Example 1 above, 30 parts by weight of Disazo Yellow and standard ink additive
Mix well with 10 parts by weight to make a color base,
Subsequently, 140 parts by weight of this color base was added to 95 parts by weight of the above petroleum hydrocarbon solvent and diluted to prepare a cyan ink.
比較例2(黄色インキの調製) 上記比較例1で得られた石油系炭化水素溶剤を用いた
こと以外は、実施例2と同様にして黄色インキを調製し
た。Comparative Example 2 (Preparation of Yellow Ink) A yellow ink was prepared in the same manner as in Example 2 except that the petroleum hydrocarbon solvent obtained in Comparative Example 1 was used.
実施例3(赤色インキの調製) 上記実施例1で得られた石油系炭化水素溶剤67重量
部,カーミン6B28重量部および標準インキ添加剤8重量
部とを充分に練り合わせてカラーベースを作り、続いて
このカラーベース120重量部を上記石油系炭化水素溶剤4
1重量部に加え希釈して赤色インキを調製した。Example 3 (Preparation of Red Ink) 67 parts by weight of the petroleum hydrocarbon solvent obtained in Example 1 above, 28 parts by weight of Carmine 6B and 8 parts by weight of standard ink additive were sufficiently kneaded to form a color base, and subsequently, 120 parts by weight of this color base is added to the above petroleum hydrocarbon solvent 4
1 part by weight was added and diluted to prepare a red ink.
比較例3(赤色インキの調製) 上記比較例1で得られた石油系炭化水素溶剤を用いた
こと以外は、実施例3と同様にして赤色インキを調製し
た。Comparative Example 3 (Preparation of Red Ink) A red ink was prepared in the same manner as in Example 3 except that the petroleum hydrocarbon solvent obtained in Comparative Example 1 was used.
実施例4(黒色インキの調製) 上記実施例1で得られた石油系炭化水素溶剤105重量
部にカーボンブラック12および標準インキ添加剤3重量
部を加えて黒色インキを調製した。Example 4 (Preparation of Black Ink) A black ink was prepared by adding 12 parts by weight of carbon black 12 and 3 parts by weight of a standard ink additive to 105 parts by weight of the petroleum hydrocarbon solvent obtained in Example 1 above.
比較例4(黒色インキの調製) 上記比較例1で得られた石油系炭化水素溶剤を用いた
こと以外は、実施例4と同様にして黒色インキを調製し
た。Comparative Example 4 (Preparation of Black Ink) A black ink was prepared in the same manner as in Example 4 except that the petroleum hydrocarbon solvent obtained in Comparative Example 1 was used.
インキの性能評価 上記実施例及び比較例で調製した各種インキについて
その性能を次の如く評価した。結果を第1表に示す。Evaluation of Ink Performance The performance of each ink prepared in the above Examples and Comparative Examples was evaluated as follows. The results are shown in Table 1.
転移性の評価 上記インキについて、版へのインキ盛り量4g/m2とし
てアート紙へ転移したインキの量(転移率)を、RIテス
ターにて測定した。Evaluation of Transferability With respect to the above ink, the amount of ink transferred to art paper (transfer rate) was measured with an RI tester with an ink amount of 4 g / m 2 on the plate.
乾燥性および浸ミトオシ性の評価 NIA式自動展色機を用い、JIS K−5702に準拠して上記
インキの乾燥性および浸ミトオシ性を測定した。乾燥性
の評価はアート紙に発色後、ただちに新らしい紙をその
上に乗せて、ブレードでこすり、この操作を繰り返して
転移が無くなるまでの回数(紙の枚数)を求めた。ここ
で第1表中の乾燥性の項目の数値は、例えば2+1/3と
は2枚の紙に転移が生じ、3枚目の紙は1/3だけ転移し
たことを示す。Evaluation of Dryability and Immersion Mitoshiki The NIA type automatic color developing machine was used to measure the dryness and immersion Mitoshiki of the above inks in accordance with JIS K-5702. For the evaluation of the drying property, immediately after coloring the art paper, a new paper was placed on it and rubbed with a blade, and this operation was repeated to determine the number of times (the number of papers) until the transfer disappeared. Here, the numerical value of the item of dryness in Table 1 is, for example, 2 + 1/3 indicates that the transfer was performed on two sheets of paper and that of the third sheet was transferred by 1/3.
なお、浸ミトオシ性の評価は比較例のインキを基準と
して表示した。In addition, the evaluation of the soaking property is based on the ink of the comparative example.
タック値の測定 THUING ALBER社製のインコメーターを用いて、32℃,4
00rpmの条件で上記インキのL値を求めた。Measurement of tack value Using a THUING ALBER incometer, 32 ℃, 4
The L value of the above ink was determined under the condition of 00 rpm.
ミスチング性の評価 THUING ALBER社製のインコメーターを用いて、32℃,1
200rpmの条件で上記インキのミスチング性を評価した。
なおこの評価は比較例のインキを基準として表示した。Evaluation of misting property Using an incommeter manufactured by THUING ALBER, 32 ° C, 1
The misting property of the above ink was evaluated under the condition of 200 rpm.
In addition, this evaluation was displayed based on the ink of the comparative example.
〔発明の効果〕 本発明の溶剤を用いれば、得られるインキは適正な流
動性,乾燥性,耐ミスチング性を有し、高速印刷及び大
量印刷に適したものとなる。 [Effects of the Invention] When the solvent of the present invention is used, the obtained ink has appropriate fluidity, drying properties and misting resistance, and is suitable for high-speed printing and mass printing.
また、この溶剤は入手の困難なナフテン基系原油から
だけでなく、パラフィン基系原油や中間基系原油からで
も高収率で容易に製造することができ、しかも%CAが小
さいため安全性が高い。Further, the solvent not only from the difficulty naphthene base crude availability, high yield can be easily produced even from paraffinic base crude and intermediate base crude, moreover% C for A is smaller safety Is high.
したがって、本発明の溶剤は各種のインキの溶剤とし
て有効に利用できることは勿論、さらに各種のペンキの
溶剤としてもその利用価値は大きい。Therefore, the solvent of the present invention can be effectively used as a solvent for various inks, and also has a great utility value as a solvent for various paints.
Claims (2)
60以上,ナフテン分含量30%以上,芳香族分含量2%以
下および流動点−20℃以下である石油系炭化水素からな
るインキ用溶剤。1. A kinematic viscosity at 40 ° C. of 0.5 to 500 cSt and a viscosity index.
An ink solvent composed of petroleum hydrocarbons having a naphthene content of 60 or more, a naphthene content of 30% or more, an aromatic content of 2% or less and a pour point of -20 ° C or less.
のものである特許請求の範囲第1項記載のインキ用溶
剤。2. The solvent for ink according to claim 1, wherein the petroleum hydrocarbon has a total acid value of 0.1 mgKOH / g or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62146240A JPH086060B2 (en) | 1987-06-13 | 1987-06-13 | Ink solvent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62146240A JPH086060B2 (en) | 1987-06-13 | 1987-06-13 | Ink solvent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63312374A JPS63312374A (en) | 1988-12-20 |
JPH086060B2 true JPH086060B2 (en) | 1996-01-24 |
Family
ID=15403270
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62146240A Expired - Lifetime JPH086060B2 (en) | 1987-06-13 | 1987-06-13 | Ink solvent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH086060B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3028679B2 (en) * | 1992-03-06 | 2000-04-04 | 東洋インキ製造株式会社 | Printing ink |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0745642B2 (en) * | 1986-07-08 | 1995-05-17 | 日本石油化学株式会社 | Solvent composition for printing ink |
-
1987
- 1987-06-13 JP JP62146240A patent/JPH086060B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS63312374A (en) | 1988-12-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101914323B (en) | Application of palm oil and palm oil derivative in ink binder | |
MXPA01005342A (en) | Lithographic printing inks comprising acid-functional vinyl polymer and polyol phase. | |
JP6243248B2 (en) | Printing ink composition | |
CN101146879B (en) | Process for producing ink composition for offset printing, and ink composition for offset printing produced by said production process | |
US2762712A (en) | Printing ink vehicle containing esterhydrocarbon copolymer drying oil | |
JP4874957B2 (en) | Method for producing ink composition for offset printing and ink composition for offset printing obtained from the production method | |
JPH086060B2 (en) | Ink solvent | |
EP1203799B1 (en) | Anti-abrasion ink additives containing reduced amounts of polytetrafluoroethylene and inks containing such additives | |
DE3132081C2 (en) | ||
JP2000212492A (en) | Resin composition for printing ink and printing ink composition | |
SU1708821A1 (en) | Dye for offset and relief printing | |
JP3880020B2 (en) | Waterless lithographic printing ink composition | |
KR101053272B1 (en) | Solvent composition for newspaper ink and its manufacturing method | |
JP3337085B2 (en) | Printing ink composition | |
DE19626723A1 (en) | Modified hydrocarbon resins | |
JP2005154669A (en) | Pigment composition and printing ink containing the same | |
CN107523125A (en) | A kind of cashew nut shell oil type ink adhesive and its ink composite | |
SU1032002A1 (en) | Ink for relief or offset printing | |
US2379950A (en) | Ink compositions | |
DE2158373C3 (en) | Printing ink oil | |
DE832295C (en) | Printing color | |
JP3443993B2 (en) | Stamp ink for stencil printing | |
JPH09169940A (en) | Ink for lithography | |
CN108864388A (en) | A kind of modified aldehyde ketone resin and preparation method thereof and a kind of emulsion ink | |
DE19626724A1 (en) | Hydrocarbon resins modified with fatty acid esters |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term | ||
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20080124 Year of fee payment: 12 |