JPS61255967A - Emulsion ink for porous printing - Google Patents

Emulsion ink for porous printing

Info

Publication number
JPS61255967A
JPS61255967A JP60099169A JP9916985A JPS61255967A JP S61255967 A JPS61255967 A JP S61255967A JP 60099169 A JP60099169 A JP 60099169A JP 9916985 A JP9916985 A JP 9916985A JP S61255967 A JPS61255967 A JP S61255967A
Authority
JP
Japan
Prior art keywords
ink
oil
emulsion
printing
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.)
Granted
Application number
JP60099169A
Other languages
Japanese (ja)
Other versions
JPH0562628B2 (en
Inventor
Toshio Matsubara
松原 俊雄
Akio Kadowaki
門脇 昭男
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.)
Riso Kagaku Corp
Original Assignee
Riso Kagaku Corp
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 Riso Kagaku Corp filed Critical Riso Kagaku Corp
Priority to JP60099169A priority Critical patent/JPS61255967A/en
Publication of JPS61255967A publication Critical patent/JPS61255967A/en
Publication of JPH0562628B2 publication Critical patent/JPH0562628B2/ja
Granted legal-status Critical Current

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  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

PURPOSE:To obtain ink which does not cause any increase in print density when, initiating printing after standing in a rotary porous printing press, and causes neither whirling up of paper nor offsetting of ink, by incorporating a solvent having a specified b.p. in the oil phase of a W/O emulsion. CONSTITUTION:The titled ink is obtd. by incorporating at least 5wt% (based on the total quantity of the water phase of an emulsion) solvent having a b.p. of 180-270 deg.C in the oil phase of a W/O emulsion consisting of 10-50wt% oil phase and 90-50wt% water phase. The b.p. (180-270 deg.C) of the solvent is higher than that of water and lower than that of non-drying oil or nonvolatile mineral oil which is the main component of the oil phase. When a solvent having a b.p. of lower than 180 deg.C is used and a porous printing press is left to stand without conducting printing over a long period of time, ink is dried on a plate cylinder to cause clogging, while when the b.p. exceeds 270 deg.C, lower ing in viscosity after standing can not be prevented as in a conventional oil phase.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、孔版印刷用エマルジョンインキに関し、さら
に詳しくは放置後の印刷濃度の増大、紙の舞い上がり、
インキの裏移りを防止した、輪転孔版印刷機、特に単胴
式孔版印刷機に好適に使用、される孔版印刷用エマルジ
ョンインキに関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to emulsion ink for stencil printing, and more specifically, to increase printing density after standing, paper flying up,
The present invention relates to an emulsion ink for stencil printing which prevents ink set-off and is suitably used in rotary stencil printing machines, particularly single cylinder stencil printing machines.

(従来の技術) 近年、輪転孔版印刷機にもマイクロコンピュータ−等に
よる自動化が進み、操作が簡単になってきており、これ
に伴ない、印刷開始直後から良好な印刷物を入手できる
ことが要望されている。
(Prior Art) In recent years, rotary stencil printing machines have become increasingly automated using microcomputers, etc., making them easier to operate.As a result, there is a demand for being able to obtain high-quality printed matter immediately after printing begins. There is.

しかしながら、従来の輪転孔版印刷機においては、オフ
セット印刷機と異なり、毎日清浄しなくてもよいように
インキを乾燥しに<<シており、そのため常時印刷を行
なっていれば1枚目から良好な印刷物が得られるが、1
晩または2.3日放置後の印刷においては、印刷濃度が
通常の印刷濃度より高く、また印刷用紙が版胴にはりつ
き、紙の舞い上がりや詰まりを生じ、さらにインキの裏
移りが多くなるという欠点があり、良好な印刷物を得る
ためにはかなりの枚数(特に単胴式孔版印刷機では時に
は1000枚以上)を刷り込まなければならないという
欠点があった。
However, in conventional rotary stencil printing machines, unlike offset printing machines, the ink is kept dry so that it does not need to be cleaned every day. However, 1
When printing overnight or after being left for 2-3 days, the printing density is higher than normal printing density, and the printing paper sticks to the plate cylinder, causing paper to fly up or jamming, and the ink to set off more often. However, in order to obtain good quality printed materials, a considerable number of sheets (especially 1,000 sheets or more in the case of a single-cylinder stencil printer) must be printed.

従来の孔版印刷用のエマルジョンインキとしては、放置
中に孔版印刷機の版胴上で乾燥して目詰まりを生じない
ように、不乾性油、不揮発性鉱油等の高沸点の溶剤(モ
ーターオイル、流動パラフィン、スピンドル油、マシン
油、ヒマシ油等)が使用されている(特公昭44−21
65号)、このエマルジョンインキが孔版印刷機内に放
置されると、エマルジョン中の水分だけが蒸発してしま
うため、水と油とのバランスがくずれ、油分の割合が増
大する。その結果、相対的に水分の割合が減少し、エマ
ルジョンインキの粘度が低下し、インキが軟化してしま
う。
Conventional emulsion ink for stencil printing uses high-boiling point solvents such as non-drying oils and non-volatile mineral oils (motor oil, liquid paraffin, spindle oil, machine oil, castor oil, etc.)
No. 65), when this emulsion ink is left in a stencil printing machine, only the water in the emulsion evaporates, which upsets the balance between water and oil and increases the proportion of oil. As a result, the proportion of water is relatively reduced, the viscosity of the emulsion ink is reduced, and the ink becomes soft.

このようにインキが軟化する結果、放置後の印刷開始時
には、インキが版胴から流れ出て、用紙に大量のインキ
が付着してしまい、前述のように印刷濃度が通常の印刷
濃度より高くなったり、また印刷用紙が版胴に貼りつく
ために、紙の舞い上がりや詰まりを生じ、さらに紙に転
移したインキが乾燥する前に次の紙が重なるため、紙の
裏側にインキが付着してインキの裏移りが多くなるとい
う現象を生じる。
As a result of this softening of the ink, when printing starts after being left unused, the ink flows out of the plate cylinder and a large amount of ink adheres to the paper, resulting in the print density being higher than the normal print density as described above. In addition, the printing paper sticks to the plate cylinder, causing paper to fly up or jam.Furthermore, the next paper overlaps with the ink transferred to the paper before it dries, causing ink to adhere to the back side of the paper and cause ink to dry. A phenomenon of increased set-off occurs.

(発明が解決しようとする問題点) 本発明の目的は、前記従来技術の欠点を除去し、輪転孔
版印刷機において、放置後の印刷開始時の印刷濃度を高
めず、紙の舞い上がりやインキの裏移りを生じない孔版
印刷用エマルジョンインキを提供することにある。
(Problems to be Solved by the Invention) An object of the present invention is to eliminate the drawbacks of the prior art described above, and to avoid increasing the print density at the start of printing after being left unused in a rotary stencil printing machine, and to prevent paper flying up and ink. To provide an emulsion ink for stencil printing that does not cause set-off.

(問題点を解決するための手段) 本発明者らは、前記目的を達成するため、種々研究の結
果、油中水型エマルジョンインキの油相中に、沸点18
0〜270℃の溶剤をエマルジョンの水相全量に対し5
重量%以上含有させることにより、エマルジョン中の水
分の蒸発とともに油分の溶剤も若干蒸発し、水と油との
比の変化量が少なく保たれ、これによりインキの粘度低
下を防止し、軟化を防止することができることを見出し
て本発明に到達した。
(Means for Solving the Problems) In order to achieve the above object, the present inventors have conducted various studies and found that the oil phase of water-in-oil emulsion ink has a boiling point of 18.
5% of the solvent at 0 to 270°C to the total amount of the aqueous phase of the emulsion.
By containing more than % by weight, as the water in the emulsion evaporates, the oil solvent also evaporates slightly, keeping the amount of change in the ratio of water to oil small, thereby preventing a decrease in the viscosity of the ink and preventing softening. The present invention was achieved by discovering that this can be done.

本発明は、油相約10〜50重量%と水相約90〜50
ffi量%とからなる油中水型エマルジョンから成り、
かつ該油相中に、該水相全量に対し5重量%以上の、沸
点180〜270℃の溶剤を含有することを特徴とする
孔版印刷用エマルジョンインキである。
The present invention has an oil phase of about 10-50% by weight and an aqueous phase of about 90-50% by weight.
Consisting of a water-in-oil emulsion consisting of ffi amount%,
The emulsion ink for stencil printing is characterized in that the oil phase contains a solvent having a boiling point of 180 to 270° C. in an amount of 5% by weight or more based on the total amount of the aqueous phase.

本発明の孔版印刷用エマルジョンインキは、油相約10
〜50重量%と水相約90〜50重量%とからなる油中
水型エマルジョンより成る。
The emulsion ink for stencil printing of the present invention has an oil phase of about 10
It consists of a water-in-oil emulsion comprising ~50% by weight of an aqueous phase and about 90-50% by weight of an aqueous phase.

前記油相は、油成分、乳化剤、着色剤、樹脂等、また前
記水相は、水、水溶性樹脂、電解質、防黴剤、水蒸発防
止剤、酸化防止剤等から構成される。
The oil phase is composed of oil components, emulsifiers, colorants, resins, etc., and the aqueous phase is composed of water, water-soluble resins, electrolytes, fungicides, water evaporation inhibitors, antioxidants, etc.

これらの各構成成分はエマルジョンの形成を阻害しない
公知のものが使用される。これらの成分中、水、油分お
よび乳化剤以外は任意成分であり、適宜添加することが
できる。
As each of these components, known components that do not inhibit emulsion formation are used. Among these components, the components other than water, oil and emulsifier are optional components and can be added as appropriate.

また本発明の孔版印刷用エマルジョンインキは。Further, the emulsion ink for stencil printing of the present invention is as follows.

前記油相中に、前記水相全量に対し、5重量%以上、好
ましくは10重量%以上の、沸点180〜270℃の溶
剤を含有する。
The oil phase contains a solvent having a boiling point of 180 to 270°C in an amount of 5% by weight or more, preferably 10% by weight or more, based on the total amount of the aqueous phase.

この溶剤の沸点180〜270℃は、水の沸点よりも高
く、かつ油相の主成分を形成する不乾性油、不揮発性鉱
油の沸点よりも低いもの(いわゆる中沸点の溶剤)であ
る。該溶剤の沸点が180℃未満であると、孔版印刷機
を印刷せずに長期放置した場合、版胴上でインキが乾燥
して目詰まりを生じてしまう。また沸点が270℃を越
えると、従来の油相の成分と変わらなくなり、放置後の
粘度低下を防止することができない。
The boiling point of this solvent is 180 to 270°C, which is higher than the boiling point of water and lower than the boiling point of the non-drying oil and non-volatile mineral oil that form the main component of the oil phase (so-called medium boiling point solvent). If the boiling point of the solvent is less than 180° C., if the stencil printing machine is left unused for a long period of time without printing, the ink will dry on the plate cylinder and cause clogging. Moreover, if the boiling point exceeds 270°C, the components will not be different from those of conventional oil phases, and it will not be possible to prevent the viscosity from decreasing after standing.

上記のような中沸点溶剤としては、沸点180〜270
℃で、インキに添加される後記樹脂を熔解させるもので
あればよく、石油系溶剤、例えばインキソルベント24
01点242〜260℃、三菱石油(株)製)、8石ア
イソゾール400(沸点206〜257℃、日本石油(
株)製)、シェルディスバゾル(沸点205〜252℃
、シェル化学(株)製)、日石4号ソルベント(沸点2
38〜267℃、日本石油(株)製)等があげられる。
The medium boiling point solvents mentioned above have a boiling point of 180 to 270.
Any petroleum solvent, such as ink solvent 24, can be used as long as it can melt the resin added to the ink at ℃.
01 point 242-260°C, produced by Mitsubishi Oil Co., Ltd.), 8-stone Isosol 400 (boiling point 206-257°C, manufactured by Nippon Oil)
Co., Ltd.), Shell Disbasol (boiling point 205-252℃)
, manufactured by Shell Chemical Co., Ltd.), Nisseki No. 4 solvent (boiling point 2
38 to 267°C, manufactured by Nippon Oil Co., Ltd.).

本発明において油相を形成する溶剤分としては、前記沸
点180〜270℃の溶剤の他に、オリーブ油、ヒマシ
油、サラダ油、イワシ油、鯨油、マシン油、スピンドル
油等の一般に油性孔版インキに用いられる不乾性油、不
揮発性鉱油が用いられる。
In the present invention, in addition to the solvents with a boiling point of 180 to 270°C, the solvents that form the oil phase include olive oil, castor oil, salad oil, sardine oil, whale oil, machine oil, spindle oil, etc. that are generally used in oil-based stencil inks. Non-drying oils and non-volatile mineral oils are used.

本発明のエマルジョンインキには、インキの保存安定性
を向上させ、インキの紙への固着、性、印刷物の刷り上
がりを良好にする等の目的で、樹脂が添加される。これ
らの樹脂としては、例えばフェノール樹脂、マレイン酸
樹脂、石油樹脂、アルキト樹脂、ゴム誘導体樹脂等が挙
げられる。またか水溶性樹脂としては、カルボキシメチ
ルセルロース、メチルセルロース、アラビアゴム等があ
げられる。これらの樹脂は水の蒸発防止効果も有する。
A resin is added to the emulsion ink of the present invention for the purpose of improving the storage stability of the ink, improving the adhesion of the ink to paper, the properties, and the quality of printed matter. Examples of these resins include phenol resins, maleic acid resins, petroleum resins, alkyto resins, and rubber derivative resins. Examples of water-soluble resins include carboxymethyl cellulose, methyl cellulose, and gum arabic. These resins also have the effect of preventing water evaporation.

また油中水型エマルジョンを構成するために用いられる
乳化剤としては、非イオン系界面活性剤が好ましく用い
られ、ソルビタン高級脂肪酸エステル(例えばソルビタ
ンモノラウレート、ソルビタンモノパルミテート、ソル
ビタンモノステアレート、ソルビタントリステアレート
、ソルビタンモノオレエート、ソルビタントリオレエー
ト、ソルビタンセスキオレエート等)、脂肪酸モノグリ
セド、例えばオレイン酸モノグリセリド、オレイン酸ジ
グリセリド、および高級アルコール、アルキルフェノー
ル、脂肪酸等の酸化エチレン付加物等があげられ、これ
らのHLBの低いものと高いものを二種以上組合せ、H
LBを調整して安定性の高いエマルジョンとすることが
できる。
In addition, as the emulsifier used to constitute the water-in-oil emulsion, nonionic surfactants are preferably used, and sorbitan higher fatty acid esters (for example, sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, sorbitan tristearate, sorbitan monooleate, sorbitan trioleate, sorbitan sesquioleate, etc.), fatty acid monoglycerides, such as oleic acid monoglyceride, oleic acid diglyceride, and ethylene oxide adducts of higher alcohols, alkylphenols, fatty acids, etc. Combining two or more of these low HLB and high HLB, H
A highly stable emulsion can be obtained by adjusting the LB.

蒸発防止剤としては、エチレングリコール、プロピレン
グリコール、ソルビトール、グリセリンなどの多価アル
コールや、ポリエチレングリコール等が用いられる。ま
た着色剤としては、例えばファーネスカーボンブラック
、ランプブランク、ブリリアントファストスカーレット
等の公知のものが用いられる。電解質としては、例えば
硫酸ナトリウム、リン酸水素ナトリウム、ホウ酸ナトリ
ウムなどが用いられる。防黴剤としては、例えばフェノ
ール類、p−オキシ安息香酸メチル、p −オキシ安息
香酸エチル等、ソルビン酸、デヒドロ酢酸、サルチル酸
等が用いられる。樹脂等の酸化防止剤としては、例えば
ジブチルヒドロキシトルエン、没食子酸プロピル、ブチ
ルヒドロキシアニソール等が用いられる。
As the evaporation inhibitor, polyhydric alcohols such as ethylene glycol, propylene glycol, sorbitol, and glycerin, polyethylene glycol, and the like are used. Further, as the coloring agent, known ones such as furnace carbon black, lamp blank, brilliant fast scarlet, etc. can be used. As the electrolyte, for example, sodium sulfate, sodium hydrogen phosphate, sodium borate, etc. are used. As the fungicide, for example, phenols, methyl p-oxybenzoate, ethyl p-oxybenzoate, sorbic acid, dehydroacetic acid, salicylic acid, etc. are used. As the antioxidant for resins, for example, dibutylhydroxytoluene, propyl gallate, butylhydroxyanisole, etc. are used.

本発明の孔版印刷用エマルジョンインキは、例えば前記
油成分と樹脂とを加熱溶解させた後、これに、着色剤お
よび乳化剤を加えて混合した後、電解質の水溶液を徐々
に添加して乳化させることにより製造することができる
。これら各成分の混合順序は、上記に限定されず、適宜
変更することができる。
The emulsion ink for stencil printing of the present invention can be prepared, for example, by heating and dissolving the oil component and resin, adding a colorant and an emulsifier to the mixture, mixing the mixture, and then gradually adding an aqueous electrolyte solution to emulsify the mixture. It can be manufactured by The mixing order of these components is not limited to the above and can be changed as appropriate.

(発明の効果) 本発明の孔版印刷用エマルジョンインキは、2.3日の
放置後でもインキの粘度低下を生じず、従って本発明の
インキを用いて輪転孔版印刷を行った場合、放置後の印
刷開始時においても、インキの過剰流出による印刷濃度
の増大、紙の舞い上がり、詰まり、インキの裏移り等を
生じることなく迅速に通常運転の状態に移行することが
できる。
(Effect of the invention) The emulsion ink for stencil printing of the present invention does not cause a decrease in ink viscosity even after being left for 2.3 days. Therefore, when rotary stencil printing is performed using the ink of the present invention, Even at the start of printing, it is possible to quickly shift to normal operation without causing an increase in printing density due to excessive ink outflow, paper flying up, clogging, ink set-off, etc.

しかも本8発明のエマルジョンインキは、従来のエマル
ジョンインキより低い沸点の溶剤を含有しているにもか
かわらず、40日程度放置しても孔版印刷機内で乾燥す
ることがない実用的なものであることが判明した。また
本発明の孔版印刷用エマルジョンインキを使用すると、
通常印刷時の裏移りも、従来のエマルジョンインキを使
用する場合に比して減少する。
Furthermore, although the emulsion ink of the present invention contains a solvent with a lower boiling point than conventional emulsion inks, it is a practical product that does not dry out in a stencil printing machine even if left for about 40 days. It has been found. Furthermore, when the emulsion ink for stencil printing of the present invention is used,
Set-off during normal printing is also reduced compared to when using conventional emulsion inks.

したがって本発明の孔版印刷用エマルジョンインキを、
輪転孔版印刷機、特に単胴式孔版印刷機に用いると、放
置後の印刷開始時においても従来より著しく少ない試し
刷り枚数で短時間に正常な印刷状態に移行することがで
き、かつ従来よりも良好な印刷物を得ることができる。
Therefore, the emulsion ink for stencil printing of the present invention,
When used in a rotary stencil printing machine, especially a single cylinder stencil printing machine, even when printing is started after being left unused, it is possible to return to a normal printing state in a short period of time with a significantly smaller number of test prints than in the past. Good printed matter can be obtained.

ト 以下、本発明を実施例および比較例によりさらに詳細に
説明する。例中の部は重量部を意味する。
The present invention will now be explained in more detail with reference to Examples and Comparative Examples. Parts in the examples mean parts by weight.

(実施例1) ファーネスカーボンブラック(着色剤)   3部イン
キソルベント 240  (溶剤)    14部ロジ
ン変性フェノール樹脂 (樹脂)9.8部ソルビタンセ
スキオレエート(乳化剤)    5部ジブチルヒドロ
キシトルエン(酸化防止剤)0.1部水       
                  65部硫酸ナト
リウム       (電解質)    3部バラオキ
シ安息香酸メチル (防黴剤)0.1部上記割合でイン
キソルベント 240およびロ   −ジン変性フェノ
ール樹脂を加熱熔解(170℃)させ、ジブチルヒドロ
キシトルエンを入れ、この混合液に、カーボンブラック
およびソルビタンセスキオレエートを混合し、3本ロー
ルで充分混練した後、これに硫酸、ナトリウム水溶液か
らなる水相を徐々に添加しながら攪拌機で攪拌して乳化
させ、本発明のエマルジョンインキを得た。
(Example 1) Furnace carbon black (colorant) 3 parts Ink Solvent 240 (solvent) 14 parts Rosin-modified phenolic resin (resin) 9.8 parts Sorbitan sesquioleate (emulsifier) 5 parts dibutylhydroxytoluene (antioxidant) 0.1 part water
65 parts Sodium sulfate (electrolyte) 3 parts Methyl oxybenzoate (anti-mold agent) 0.1 part Ink Solvent 240 and rosin-modified phenol resin in the above ratio were melted by heating (170°C), dibutylhydroxytoluene was added, Carbon black and sorbitan sesquioleate are mixed into this liquid mixture, thoroughly kneaded with three rolls, and then an aqueous phase consisting of sulfuric acid and an aqueous sodium solution is gradually added thereto while stirring with a stirrer to emulsify the mixture. An inventive emulsion ink was obtained.

このエマルジョンインキを単胴式輪転孔版印刷機リソグ
ラフAP7200 (理想科学工業(株)製)に供給し
、十分印刷を行なってインキを印刷機内にいきわたらせ
、48時間放置後印刷を再開した。この際の印刷物の印
刷濃度を反射式光学濃度針(大日本スクリーン社製DM
−400)によって測定し、その結果を第1図に示した
。第1図中の横軸は放置後の印刷枚数を、また縦軸は光
学濃度を示したものである。なお通常状態の印刷濃度は
0.7である。
This emulsion ink was supplied to a single-cylinder rotary stencil printer RISOGRAPH AP7200 (manufactured by Riso Kagaku Kogyo Co., Ltd.), sufficient printing was carried out to spread the ink throughout the printing press, and printing was resumed after being left for 48 hours. At this time, the print density of the printed matter is measured using a reflective optical density needle (DM made by Dainippon Screen Co., Ltd.).
-400), and the results are shown in FIG. In FIG. 1, the horizontal axis shows the number of prints after being left and the vertical axis shows the optical density. Note that the printing density in the normal state is 0.7.

(比較例1) ファーネスカーボンブラック        3部スピ
ンドル油(沸点270〜378℃)   12部ロジン
変性フェノール樹脂        9.8部ソルビタ
ンセスキオレエート        5部ジブチルヒド
ロキシトルエン       0.1部水      
                   67部硫酸ナ
トリウム               3部バラオキ
シ安息香酸メチル        0.1部上記化合物
を用い、その他は実施例1と同様にして乳化させて比較
例1のエマルジョンインキを得た。これをリソグラフA
P7200に入れ、実施例1と同様にして放置後印刷を
行なった。結果を第1図に示す。
(Comparative Example 1) Furnace carbon black 3 parts Spindle oil (boiling point 270-378°C) 12 parts Rosin-modified phenolic resin 9.8 parts Sorbitan sesquioleate 5 parts Dibutylhydroxytoluene 0.1 part Water
67 parts Sodium sulfate 3 parts Methyl hydroxybenzoate 0.1 part Emulsification was carried out in the same manner as in Example 1 except that the above compound was used to obtain an emulsion ink of Comparative Example 1. This is risograph A
P7200, and after being left to stand, printing was performed in the same manner as in Example 1. The results are shown in Figure 1.

実施例2 ブリリアントファストスカーレット     3部日石
アイソゾール 400         14部アルキ
ド樹脂               9部ソルビタン
モノオレエート         49部ブチルヒドロ
キシアニソール       0.1 部水     
                    60部エチ
レングリコール            5部ホウ酸ナ
トリウム              1部カルボギシ
メチルセルロース        3部上記化合物を用
い、その他は実施例1と同様にして乳化させて本発明の
エマルジョンインキを得た。これをリソグラフAP72
00に入れ、実施例1と同様にして放置後印刷を行なっ
た。結果は第1図における実施例1と同様な曲線が得ら
れた。
Example 2 Brilliant Fast Scarlet 3 parts Nisseki Isosol 400 14 parts Alkyd resin 9 parts Sorbitan monooleate 49 parts Butyl hydroxyanisole 0.1 part Water
60 parts ethylene glycol 5 parts sodium borate 1 part carboxymethyl cellulose 3 parts Emulsification was carried out in the same manner as in Example 1 except that the above compound was used to obtain an emulsion ink of the present invention. This is RISOGRAPH AP72
00, and after being left to stand, printing was performed in the same manner as in Example 1. As a result, a curve similar to that of Example 1 in FIG. 1 was obtained.

(実施例3) ファーネスカーボンブラック        3部イン
キソルベント 240        7部スピンドル
油               7部ロジン変性フェ
ノール樹脂        9.8部ソルビタンセスキ
オレエート         5部ジブチルヒドロキシ
トルエン       0.1部水         
                 65部硫酸ナトリ
ウム               3部バラオキシ安
息香酸メチル        0.1部上記化合物を用
い、その他は実施例1と同様にして乳化させて本発明の
エマルジョンインキを得た。これをリソグラフAP72
00に入れ、実施例1と同様にして放置後印刷を行なっ
た。結果を第1図に示す。
(Example 3) Furnace carbon black 3 parts Ink solvent 240 7 parts Spindle oil 7 parts Rosin-modified phenolic resin 9.8 parts Sorbitan sesquioleate 5 parts Dibutylhydroxytoluene 0.1 part Water
65 parts Sodium sulfate 3 parts Methyl dioxybenzoate 0.1 part The emulsion ink of the present invention was obtained by emulsifying the above compound in the same manner as in Example 1 except that the above compound was used. This is RISOGRAPH AP72
00, and after being left to stand, printing was performed in the same manner as in Example 1. The results are shown in Figure 1.

(実施例4) ファーネスカーボンブラック        3部イン
キソルベント 240        5.6部スピン
ドル油              8.4部ロジン変
性フェノール樹脂        9.8部ソルビタン
セスキオレエート         5部ジブチルヒド
ロキシトルエン       0.1部水      
                   65部硫酸ナ
トリウム               3部バラオキ
シ安息香酸メチル        0.1部上記化合物
を用い、その他は実施例1と同様にして乳化させて本発
明のエマルジョンインキを得た。これをリソグラフAP
7200に入れ、実施例1と同様にして放置後印刷を行
なった。その結果を第1図に示す。
(Example 4) Furnace carbon black 3 parts Ink solvent 240 5.6 parts Spindle oil 8.4 parts Rosin modified phenolic resin 9.8 parts Sorbitan sesquioleate 5 parts Dibutyl hydroxytoluene 0.1 part Water
65 parts Sodium sulfate 3 parts Methyl dioxybenzoate 0.1 part The emulsion ink of the present invention was obtained by emulsifying the above compound in the same manner as in Example 1 except that the above compound was used. Apply this to Risograph AP
7200, and after being left to stand, printing was performed in the same manner as in Example 1. The results are shown in FIG.

(実施例5) ファーネスカーボンブラック        3部イン
キソルベント 240        4.2部スピン
ドル油              9.8部ロジン変
性フェノール樹脂        9.8部ソルビタン
セスキオレエート         5部ジブチルヒド
ロキシトルエン       0.1部水      
                   65部硫酸ナ
トリウム               3部パラオキ
シ安息香酸メチル        0.1部上記化合物
を用い、その他は実施例1と同様にして乳化させて本発
明のエマルジョンインキを得た。これをリングラフAP
?200に入れ、実施例1と同様にして放置後印刷を行
なった。結果を第1図に示す。
(Example 5) Furnace carbon black 3 parts Ink Solvent 240 4.2 parts Spindle oil 9.8 parts Rosin modified phenolic resin 9.8 parts Sorbitan sesquioleate 5 parts Dibutylhydroxytoluene 0.1 part Water
65 parts Sodium sulfate 3 parts Methyl paraoxybenzoate 0.1 part Emulsification was carried out in the same manner as in Example 1 except that the above compound was used to obtain an emulsion ink of the present invention. Apply this to Ring Graph AP
? 200, and after being left to stand, printing was performed in the same manner as in Example 1. The results are shown in Figure 1.

(比較例2) ファーネスカーボンブラック        3部イン
キソルベント 240        2.8部スピン
ドル油             11.2部ロジン変
性フェノール樹脂        9.8部ソルビタン
セスキオレエート        5部ジブチルヒドロ
キシトルエン       0.1部水       
                  65部硫酸ナト
リウム               3部パラオキシ
安息香酸メチル        0.1部上記化合物を
用い、その他は実施例1と同様にして乳化させてエマル
ジョンインキを得た。これをリソグラフAP7200に
入れ、実施例1と同様にして放置後印刷を行なった。結
果を第1図に示す。
(Comparative Example 2) Furnace carbon black 3 parts Ink Solvent 240 2.8 parts Spindle oil 11.2 parts Rosin modified phenolic resin 9.8 parts Sorbitan sesquioleate 5 parts Dibutylhydroxytoluene 0.1 part Water
65 parts Sodium sulfate 3 parts Methyl paraoxybenzoate 0.1 part Emulsification was carried out in the same manner as in Example 1 except that the above compound was used to obtain an emulsion ink. This was placed in a RISOGRAPH AP7200 and printed after being left in the same manner as in Example 1. The results are shown in Figure 1.

第1図の結果から明らかなように、比較例1の不揮発性
鉱油を使用したエマルジョンインキの場合には放置後の
最初の印刷濃度が通常印刷物の濃度に比して0.35も
高く、しかも通常状態の印刷濃度になるまでに1600
枚以上も印刷する必要があるのに対し、本発明のエマル
ジョンインキの場合には、初めの印刷物の濃度が通常状
態に比して0.1〜0.18 Lか高くならず、また1
00枚でほとんど放置前の印刷濃度と変わらない程度の
濃度に戻る。
As is clear from the results in Figure 1, in the case of the emulsion ink using non-volatile mineral oil of Comparative Example 1, the initial printing density after standing was 0.35 higher than that of normal printed matter. 1600 to reach normal printing density
In contrast, in the case of the emulsion ink of the present invention, the density of the first printed matter is only 0.1 to 0.18 L higher than the normal state, and
After printing 00 sheets, the print density returns to almost the same level as the print density before being left unused.

また本発明の場合には、紙の舞い上がりや詰まりも起こ
らず、裏移りの程度も通常印刷時と変わらなかった。
Further, in the case of the present invention, neither paper flying up nor jamming occurred, and the degree of set-off was also the same as in normal printing.

また第1図の結果から明らかなように、沸点180〜2
70℃の溶剤を、水相全量に対し5重量%未滴の割合で
含有させる比較例2の場合には、本発明のエマルジョン
インキを用いる場合に比して、放置後の最初の印刷濃度
が高く、しかも通常状態の印刷濃度になるまでの印刷枚
数もかなり多い。
Also, as is clear from the results in Figure 1, the boiling point is 180~2
In the case of Comparative Example 2, in which the solvent at 70° C. is contained in a droplet proportion of 5% by weight based on the total amount of the aqueous phase, the initial printing density after standing is lower than that in the case of using the emulsion ink of the present invention. The printing density is high, and the number of prints required to reach the normal print density is also quite large.

なお実施例1および比較例1のエマルジョンインキの、
放置前および放置後のインキ粘度の測定値は第1表の通
りであった。インキ粘度はスプレッドメーターによる「
1分値(30℃)」(試験開始1分経過時の直径の大き
さ)で示した。
Note that the emulsion inks of Example 1 and Comparative Example 1,
The measured values of ink viscosity before and after standing were shown in Table 1. Ink viscosity is measured using a spread meter.
1 minute value (30°C) (diameter size after 1 minute has passed from the start of the test).

第    1    表 第1表の結果から、実施例1の場合には、放置後のイン
キ粘度は、放置前のインキ粘度に比して若干軟化するが
、比較例1の場合に比して粘度低下がきわめて少ないこ
とかわる。
Table 1 From the results in Table 1, in the case of Example 1, the ink viscosity after standing was slightly softened compared to the ink viscosity before standing, but the viscosity decreased compared to Comparative Example 1. The difference is that there are very few.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、本発明のエマルジョンインキを用いて48時
間放置した後に印刷開始した場合の印刷濃度の測定結果
を示す図面である。
FIG. 1 is a diagram showing the measurement results of printing density when printing was started after leaving the emulsion ink of the present invention for 48 hours.

Claims (1)

【特許請求の範囲】[Claims] (1)油相約10〜50重量%と水相約90〜50重量
%とからなる油中水型エマルジョンから成り、かつ該油
相中に、該水相全量に対し5重量%以上の、沸点180
〜270℃の溶剤を含有することを特徴とする孔版印刷
用エマルジョンインキ。
(1) Consists of a water-in-oil emulsion consisting of about 10 to 50% by weight of an oil phase and about 90 to 50% by weight of an aqueous phase, and in the oil phase, 5% by weight or more based on the total amount of the aqueous phase has a boiling point of 180%.
An emulsion ink for stencil printing characterized by containing a solvent at ~270°C.
JP60099169A 1985-05-10 1985-05-10 Emulsion ink for porous printing Granted JPS61255967A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60099169A JPS61255967A (en) 1985-05-10 1985-05-10 Emulsion ink for porous printing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60099169A JPS61255967A (en) 1985-05-10 1985-05-10 Emulsion ink for porous printing

Publications (2)

Publication Number Publication Date
JPS61255967A true JPS61255967A (en) 1986-11-13
JPH0562628B2 JPH0562628B2 (en) 1993-09-08

Family

ID=14240145

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60099169A Granted JPS61255967A (en) 1985-05-10 1985-05-10 Emulsion ink for porous printing

Country Status (1)

Country Link
JP (1) JPS61255967A (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63277287A (en) * 1987-05-08 1988-11-15 Ricoh Co Ltd Stencil printing ink
JPH0649401A (en) * 1992-07-28 1994-02-22 Tohoku Ricoh Co Ltd Emulsion ink for stencil printing
JPH06329970A (en) * 1993-05-19 1994-11-29 Tohoku Ricoh Co Ltd Emulsion ink for stencil printing
US5378739A (en) * 1991-11-01 1995-01-03 Ricoh Company, Ltd. Emulsion ink for use in stencil printing
EP0694595A1 (en) 1994-07-25 1996-01-31 Riso Kagaku Corporation Emulsion ink for stencil printing
EP0704506A1 (en) 1994-09-29 1996-04-03 Riso Kagaku Corporation Stencil printing emulsion ink
EP0726300A1 (en) 1995-02-13 1996-08-14 Riso Kagaku Corporation Emulsion ink for stencil printing
JPH0940897A (en) * 1995-07-27 1997-02-10 Tohoku Ricoh Co Ltd Emulsion ink for stencil printing and printer therefor
US5622548A (en) * 1995-05-19 1997-04-22 Micap Technology Corp. Duplicating inks for digital duplicators
EP0778323A2 (en) 1995-12-05 1997-06-11 Riso Kagaku Corporation An emulsion ink for stencil printing
EP0786502A2 (en) 1996-01-26 1997-07-30 Riso Kagaku Corporation Emulsion ink for stencil printing
US5759245A (en) * 1996-02-26 1998-06-02 Riso Kagaku Corporation Emulsion ink for stencil printing
US5776232A (en) * 1996-03-14 1998-07-07 Riso Kagaku Corporation Emulsion ink for stencil printing
US5779777A (en) * 1996-03-26 1998-07-14 Riso Kagaku Corporation Emulsion ink for stencil printing
US5904759A (en) * 1996-12-10 1999-05-18 Riso Kagaku Corporation Process and apparatus for preparing emulsion ink for stencil printing
US6011083A (en) * 1996-06-18 2000-01-04 Riso Kagaku Corporation Emulsion ink for stencil printing
US6190444B1 (en) 1998-10-19 2001-02-20 Riso Kagaku Corporation Emulsion ink for stencil printing
US6348519B1 (en) * 1995-05-02 2002-02-19 Ricoh Company, Ltd. Emulsion ink and printing method using emulsion ink
US6663701B2 (en) 2001-01-26 2003-12-16 Riso Kagaku Corporation Emulsion ink for stencil printing and its use
JP2016120622A (en) * 2014-12-24 2016-07-07 セイコーエプソン株式会社 Inkjet recording method and ink set

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US2754218A (en) * 1953-04-27 1956-07-10 Il William A Magie Printing ink
US3421910A (en) * 1964-11-10 1969-01-14 Dick Co Ab Stencil duplicating paste ink
JPS527370A (en) * 1975-07-01 1977-01-20 Asahi Glass Co Ltd Process for decomposing organic compounds containing halogens
JPS5527355A (en) * 1978-08-17 1980-02-27 Fuji Photo Film Co Ltd Developing ink composition for lithographic plate
JPS57202360A (en) * 1981-06-08 1982-12-11 Sakura Color Prod Corp Emulsion type colorant composition
JPS5998890A (en) * 1982-11-29 1984-06-07 Pentel Kk Color mixing inhibiting composition for screen printing

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2754218A (en) * 1953-04-27 1956-07-10 Il William A Magie Printing ink
US3421910A (en) * 1964-11-10 1969-01-14 Dick Co Ab Stencil duplicating paste ink
JPS527370A (en) * 1975-07-01 1977-01-20 Asahi Glass Co Ltd Process for decomposing organic compounds containing halogens
JPS5527355A (en) * 1978-08-17 1980-02-27 Fuji Photo Film Co Ltd Developing ink composition for lithographic plate
JPS57202360A (en) * 1981-06-08 1982-12-11 Sakura Color Prod Corp Emulsion type colorant composition
JPS5998890A (en) * 1982-11-29 1984-06-07 Pentel Kk Color mixing inhibiting composition for screen printing

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63277287A (en) * 1987-05-08 1988-11-15 Ricoh Co Ltd Stencil printing ink
US5378739A (en) * 1991-11-01 1995-01-03 Ricoh Company, Ltd. Emulsion ink for use in stencil printing
JPH0649401A (en) * 1992-07-28 1994-02-22 Tohoku Ricoh Co Ltd Emulsion ink for stencil printing
JPH06329970A (en) * 1993-05-19 1994-11-29 Tohoku Ricoh Co Ltd Emulsion ink for stencil printing
EP0694595A1 (en) 1994-07-25 1996-01-31 Riso Kagaku Corporation Emulsion ink for stencil printing
EP0704506A1 (en) 1994-09-29 1996-04-03 Riso Kagaku Corporation Stencil printing emulsion ink
CN1051568C (en) * 1994-09-29 2000-04-19 理想科学工业株式会社 Stencil printing emulsion ink
US5573578A (en) * 1994-09-29 1996-11-12 Riso Kagaku Corporation Stencil printing emulsion ink
EP0726300A1 (en) 1995-02-13 1996-08-14 Riso Kagaku Corporation Emulsion ink for stencil printing
US6348519B1 (en) * 1995-05-02 2002-02-19 Ricoh Company, Ltd. Emulsion ink and printing method using emulsion ink
US5622548A (en) * 1995-05-19 1997-04-22 Micap Technology Corp. Duplicating inks for digital duplicators
JPH0940897A (en) * 1995-07-27 1997-02-10 Tohoku Ricoh Co Ltd Emulsion ink for stencil printing and printer therefor
EP0778323A2 (en) 1995-12-05 1997-06-11 Riso Kagaku Corporation An emulsion ink for stencil printing
US5738715A (en) * 1995-12-05 1998-04-14 Riso Kagaku Corporation Emulsion ink for stencil printing
US5718748A (en) * 1996-01-26 1998-02-17 Riso Kagaku Corporation Emulsion ink for stencil printing
EP0786502A2 (en) 1996-01-26 1997-07-30 Riso Kagaku Corporation Emulsion ink for stencil printing
US5759245A (en) * 1996-02-26 1998-06-02 Riso Kagaku Corporation Emulsion ink for stencil printing
US5776232A (en) * 1996-03-14 1998-07-07 Riso Kagaku Corporation Emulsion ink for stencil printing
US5779777A (en) * 1996-03-26 1998-07-14 Riso Kagaku Corporation Emulsion ink for stencil printing
US6011083A (en) * 1996-06-18 2000-01-04 Riso Kagaku Corporation Emulsion ink for stencil printing
US5904759A (en) * 1996-12-10 1999-05-18 Riso Kagaku Corporation Process and apparatus for preparing emulsion ink for stencil printing
US6190444B1 (en) 1998-10-19 2001-02-20 Riso Kagaku Corporation Emulsion ink for stencil printing
US6663701B2 (en) 2001-01-26 2003-12-16 Riso Kagaku Corporation Emulsion ink for stencil printing and its use
JP2016120622A (en) * 2014-12-24 2016-07-07 セイコーエプソン株式会社 Inkjet recording method and ink set

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