JPS6025467B2 - Method for producing coloring agent ink for carbon-free paper - Google Patents

Method for producing coloring agent ink for carbon-free paper

Info

Publication number
JPS6025467B2
JPS6025467B2 JP50018155A JP1815575A JPS6025467B2 JP S6025467 B2 JPS6025467 B2 JP S6025467B2 JP 50018155 A JP50018155 A JP 50018155A JP 1815575 A JP1815575 A JP 1815575A JP S6025467 B2 JPS6025467 B2 JP S6025467B2
Authority
JP
Japan
Prior art keywords
printing
coloring agent
carbon
free paper
agent ink
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
Application number
JP50018155A
Other languages
Japanese (ja)
Other versions
JPS5194308A (en
Inventor
泰山 新谷
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.)
Toppan Edge Inc
Original Assignee
Toppan Moore 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 Toppan Moore Co Ltd filed Critical Toppan Moore Co Ltd
Priority to JP50018155A priority Critical patent/JPS6025467B2/en
Publication of JPS5194308A publication Critical patent/JPS5194308A/en
Publication of JPS6025467B2 publication Critical patent/JPS6025467B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明はノーカーボン紙用呈色剤印刷インキの製造法に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing colorant printing inks for carbonless paper.

従来ノーカーボン紙の呈色剤の部分印刷に於いてその印
刷インキはメタノール、インブロピルアルコールまたは
メチルエチルケトンなどの揮発性溶剤が使用されている
が、この場合、濃度管理、毒性、引火性や又その低粘度
の故にグラビャ印刷やフレキソ印刷方式に於ける使用に
限られていて、凸版印刷や平版印刷には使用できなかっ
た。
Conventionally, volatile solvents such as methanol, imbropyl alcohol, or methyl ethyl ketone have been used as printing inks for partial printing of colorants on carbonless paper, but in this case, concentration control, toxicity, flammability, and Due to its low viscosity, its use is limited to gravure printing and flexographic printing, and it cannot be used for letterpress printing or planographic printing.

又従来のノーカーボン紙用呈色剤印刷インキは呈色剤と
して活性白土、カオリン、ベントナィトなどの天然固体
酸やノボラック型の酸性重合体を受光剤がバインダーと
共に上記低沸点溶剤に溶解し、或は混合して用紙にグラ
ビヤ印刷やフレキソ印刷方式で印刷していた。従って低
沸点溶剤を用いる印刷形式であるため濃度を一定に保持
するための管理や毒性、引火性などのためまた印刷方式
上の止むを得ない制約等の問題があった。平版印刷又は
凸版印刷用の呈色剤印刷インキも考案されているが、(
特公昭49一5930号)印刷適性が悪く、発色も微弱
であるために実用にはならなかった。本発明は前述の諸
欠点を著しく改善して凸版印刷や平版印刷においても印
刷適性が良好でしかも発色性が殴れ、その鮮明度が長期
保持されるなど著しく改善された優秀なノーカーボン紙
用呈色剤印刷インキの製造を可能ならしめたものである
Conventional color-forming printing inks for carbonless paper use natural solid acids such as activated clay, kaolin, bentonite, and novolac-type acidic polymers as color-forming agents, and light-receiving agents that are dissolved in the above-mentioned low boiling point solvent together with a binder. were mixed and printed on paper using gravure printing or flexo printing. Therefore, since the printing method uses a low boiling point solvent, there are problems such as management to keep the concentration constant, toxicity, flammability, etc., and unavoidable restrictions on the printing method. Color-forming printing inks for planographic printing or letterpress printing have also been devised;
(Japanese Patent Publication No. 49-5930) It was not suitable for printing and the color development was weak, so it was not put to practical use. The present invention significantly improves the above-mentioned drawbacks and provides an excellent carbonless paper that has good printability even in letterpress printing and lithographic printing, has excellent color development, and maintains its sharpness for a long period of time. This makes it possible to produce color printing inks.

今まで凸版や平版用のこれら星色剤用スポットインキが
できなかった大きな理由はビヒクルが呈色剤を包み込ん
でしまい、更にはこのビヒクルの成分が発色を阻害する
ような物質を含んでいる場合がある。例えば植物油脂等
のグリセラィド類の有するC=○結合は染料の発色を阻
害する。そのため、これらを用いた場合発色してもすぐ
に退色してしまうことであった。又C=0結合がない長
い長鎖状構造である合成童合乾性油(特公昭49−59
3ぴ号)を用いた場合退色はいこくいが発色が充分な濃
度とならない上に印刷適正も良好なものではなかつた。
このC=○結合のある物質のために退色することについ
ては通常のノーカーボン紙に発色させた後、その上にC
=○結合を有する物質を塗布してその発色の変化を見て
判断することができる。
The main reason why spot inks for star coloring agents for letterpress and lithographic printing have not been possible until now is that the vehicle envelops the coloring agent, and furthermore, the components of this vehicle may contain substances that inhibit color development. There is. For example, the C=○ bond of glycerides such as vegetable oils and fats inhibits the color development of dyes. Therefore, when these were used, even if the color was developed, the color would quickly fade. In addition, synthetic doji drying oil (Special Publication No. 49-59
When using No. 3P), there was little fading, but the color development did not have sufficient density, and the printability was not good either.
Regarding fading due to substances with this C=○ bond, after developing the color on ordinary carbonless paper, add C on top of it.
It can be determined by coating a substance with =○ bond and observing the change in color.

即ち赤外線分光光度計で測定して1700肌‐1付近の
吸収でC=○結合の存在を示すような物質を使用を避け
なければならない。植物性油脂はいづれもC=○結合を
有する。
That is, it is necessary to avoid using substances that show the presence of a C=◯ bond when measured with an infrared spectrophotometer and have an absorption around 1700 skin-1. All vegetable oils and fats have a C=○ bond.

本発明方法に於いてはノーカーボン紙における呈色剤で
ある酸性重合体、主としてノボラック系フェノール樹脂
の溶剤ともなりかつ発色剤用染料の溶剤でもあり、不揮
発性であって、印刷適正の良好な溶剤を種々検討した結
果、インプロピルナフタレン類及びジフェニルメタン類
が優れた成績を示すことを発見するに至った。インプロ
ピルナフタレン類は下式に示す如きものでその中とくに
下式に示すm、{21、{3’、‘4’式のものが推奨
される。
In the method of the present invention, the acidic polymer, which is the coloring agent in carbonless paper, serves as a solvent for mainly novolak phenolic resin and also as a solvent for the coloring agent dye, and is nonvolatile and has good printability. As a result of examining various solvents, it was discovered that inpropylnaphthalenes and diphenylmethanes showed excellent results. The inpropylnaphthalenes are as shown in the following formula, and among these, those of m, {21, {3', and '4' formulas as shown in the following formula are particularly recommended.

これら一連の化合物は単独又は混合して使用することが
でき、またジフェニルメタン類は次式 で示されるがその中とくにメチルフェニルキシリルメタ
ン類が良好な成績を示すが下記の【11式及び■式で示
される物質は極めて良好な結果を示した。
These series of compounds can be used alone or in combination, and diphenylmethanes are shown by the following formulas, among which methylphenylxylylmethanes have shown particularly good results. The substance shown in shows extremely good results.

これらの溶剤はノーカーボン紙の発色剤用染料の溶剤と
して利用されていたが、インキのピヒクルという分野に
おいては従来用いられていなかった。
These solvents have been used as solvents for coloring dyes in carbonless paper, but have not been used in the field of ink vehicles.

事実常温では該酸性重合体はこれら溶剤には溶解しにく
いが、加熱することによりて溶解して釆る。
In fact, the acidic polymer is difficult to dissolve in these solvents at room temperature, but it dissolves and boils when heated.

またこの溶液は再び常温まで冷却しても溶解した該酸性
重合体は析出してこないことも確認した。勿論その溶解
度や析出の範囲については自ら限界のあるものである。
しかしこの酸性重合体のこれら溶剤への溶解による適当
な粘度の上昇によりインキの印刷適性が著しく良好にな
るので凸版や平版印刷が可能になった。これらの溶液は
発色を阻害する物質でなく、不揮発性であり粘度は適当
に高く、毒性も知られていないので、凸版や平版印刷イ
ンク用ビヒクルとして最適で、発色を妨げる要素を含ま
ないので退色も認められず鮮明な記録を長期間保持でき
るものである。
It was also confirmed that the dissolved acidic polymer did not precipitate even if this solution was cooled to room temperature again. Of course, there are limits to its solubility and precipitation range.
However, by appropriately increasing the viscosity by dissolving the acidic polymer in these solvents, the printability of the ink becomes significantly better, making letterpress and lithographic printing possible. These solutions do not contain substances that inhibit color development, are non-volatile, have moderately high viscosity, and are not known to be toxic, making them ideal as vehicles for letterpress and lithographic printing inks, and do not contain any elements that inhibit color development, so they do not fade. It is possible to keep clear records for a long time without being recognized.

次に実施例について述べる。Next, an example will be described.

実施例 1 KMC−オイル(商品名、インプロピルナフタレン、呉
羽化学社製)2kgをCKM−5254(商品名、パラ
フェニルフェノールホルムアルデヒド樹脂、昭和ユニオ
ン社製)1.5k9に100午 Cに加熱して溶解して
ビヒクルを製造した。
Example 1 2 kg of KMC-oil (trade name, inpropyl naphthalene, manufactured by Kureha Chemical Co., Ltd.) was heated to 1.5k9 at 100 pm CKM-5254 (trade name, paraphenylphenol formaldehyde resin, manufactured by Showa Union Co., Ltd.). The vehicle was prepared by dissolution.

これに白色顔料としてチタン白210g(ビヒクルの6
%)を混合してインキとする。
Add to this 210 g of titanium white as a white pigment (6
%) to make ink.

これを印刷機で平版印刷して仕上げ、市販のノーカーボ
ンカプセル紙と対向させて印字したところ発色は強力で
退色は30日間室内で放置しても見られなかった。印刷
適性も極めて良好であった。乾燥も浸透による乾燥で早
く、かつ紙面からのインキの剥離も見られなかった。
When this was finished by lithographic printing using a printing machine and printed against commercially available carbonless capsule paper, the color development was strong and no fading was observed even after being left indoors for 30 days. Printability was also extremely good. Drying was quick due to osmosis, and no peeling of the ink from the paper surface was observed.

実施例 2 KMCーオィル(商品名、前世)、lk9と/・ィゾー
ルSAS(商品名、メチルフェニルキシリルメタン、日
本石油化学社製)lk9を混合しCKM−5254(前
出、/ボラツク樹脂)2k9を10び○で加熱溶解して
ビヒクルとする。
Example 2 KMC-Oil (trade name, previous generation), lk9 and /-Isol SAS (trade name, methylphenylxylylmethane, manufactured by Nippon Petrochemicals) lk9 were mixed to make CKM-5254 (mentioned above, /volac resin) 2k9. A vehicle is prepared by heating and dissolving at 10℃.

これに白色顔料としてチタン白240g(ビヒクルの6
%)を加えてノーカーポン紙用呈色インキを製造した。
これを印刷機で平版印刷して仕上げ、市販のノーカーボ
ンカプセル紙と対向させ印字したところ発色は非常に鮮
明で30日間室内で放置して退色は全く認められなかっ
た。尚印刷適性は実施例1と同機極めて良好であった。
Add to this 240 g of titanium white as a white pigment (6
%) to produce a colored ink for non-carbon paper.
This was finished by planographic printing using a printing machine, and when printed against commercially available carbonless capsule paper, the color development was very clear and no fading was observed even after being left indoors for 30 days. The printability of the same machine as in Example 1 was extremely good.

本発明方法によって作られたノーカーボン紙用呈色剤イ
ンキによる印刷に於いては特別な印刷装置を必要とせず
、全面印刷も部分印刷も容易に実施できる上にコストダ
ウンができ、毒性、引火性、濃度管理等の従来の諸問題
も解決され、そのため印刷オペレーター数も減少させる
ことができ、製品が安定したものとなった。
Printing with the coloring agent ink for carbonless paper produced by the method of the present invention does not require any special printing equipment, can easily perform full-scale printing or partial printing, can reduce costs, and is free from toxicity and flammability. Conventional problems such as quality and density control have also been resolved, and the number of printing operators has therefore been reduced, making the product more stable.

Claims (1)

【特許請求の範囲】[Claims] 1 発色剤用染料並びに呈色剤用酸性重合体を共に溶解
することのできるイソプロピルナフタレン類又はジフエ
ニルメタン類のそれぞれ単独又はそれらの混合物に酸性
重合体を溶解してなるビヒクルと顔料とを混合すること
を特徴とするノーカーボン紙用呈色剤インキの製造法。
1. Mixing a pigment with a vehicle obtained by dissolving an acidic polymer in isopropylnaphthalenes or diphenylmethanes, each singly or in a mixture thereof, which can dissolve both the dye for the color former and the acidic polymer for the color former. A method for producing coloring agent ink for carbonless paper, characterized by:
JP50018155A 1975-02-13 1975-02-13 Method for producing coloring agent ink for carbon-free paper Expired JPS6025467B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50018155A JPS6025467B2 (en) 1975-02-13 1975-02-13 Method for producing coloring agent ink for carbon-free paper

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50018155A JPS6025467B2 (en) 1975-02-13 1975-02-13 Method for producing coloring agent ink for carbon-free paper

Publications (2)

Publication Number Publication Date
JPS5194308A JPS5194308A (en) 1976-08-18
JPS6025467B2 true JPS6025467B2 (en) 1985-06-18

Family

ID=11963713

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50018155A Expired JPS6025467B2 (en) 1975-02-13 1975-02-13 Method for producing coloring agent ink for carbon-free paper

Country Status (1)

Country Link
JP (1) JPS6025467B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62238785A (en) * 1986-04-09 1987-10-19 Kureha Chem Ind Co Ltd Pressure sensitive paper

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5156315A (en) * 1974-11-12 1976-05-18 Kureha Chemical Ind Co Ltd

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5156315A (en) * 1974-11-12 1976-05-18 Kureha Chemical Ind Co Ltd

Also Published As

Publication number Publication date
JPS5194308A (en) 1976-08-18

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