JPS60243173A - Ink composition for marking sterilization with ethylene oxide - Google Patents

Ink composition for marking sterilization with ethylene oxide

Info

Publication number
JPS60243173A
JPS60243173A JP59099292A JP9929284A JPS60243173A JP S60243173 A JPS60243173 A JP S60243173A JP 59099292 A JP59099292 A JP 59099292A JP 9929284 A JP9929284 A JP 9929284A JP S60243173 A JPS60243173 A JP S60243173A
Authority
JP
Japan
Prior art keywords
acid
sterilization
ink composition
ethylene oxide
pigment
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.)
Pending
Application number
JP59099292A
Other languages
Japanese (ja)
Inventor
Masashi Yamamoto
山本 雅司
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.)
Sakura Color Products Corp
Original Assignee
Sakura Color Products 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 Sakura Color Products Corp filed Critical Sakura Color Products Corp
Priority to JP59099292A priority Critical patent/JPS60243173A/en
Publication of JPS60243173A publication Critical patent/JPS60243173A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:The titled composition that is composed of a pigment with a specific chemical structure, a resin such as polyacrylic acid and a polar solvent, thus being used in printing ink with color change retardation in case of moisture absence. CONSTITUTION:The objective composition is obtained by using a pigment of the formula (A is ethylene residue, O-phenylene residue; R1, R2 are H, lower alkyl, hydroxy-lower alkyl), when needed, a small amount of usual pigment for color adjusting, one or more binder resins, selected from polyacrylic acid, polymethacrylic acid and copolymer therefrom, a polar solvent such as ethanol, when needed an organic acid such as oxalic acid, a surfactant, preservative and anticorrosive.

Description

【発明の詳細な説明】 本発明はエチレンオキサイド滅菌標識用インキ組成物に
関する。そしてこのインキ組成物は印刷用インキとして
、あるいはマーキンブチレンオキサイドにより行なわれ
ている。これら滅菌方法により滅菌を行なう場合、滅菌
が完全に行なわれたか否かを識別するために、滅菌条件
に達したとき変色するインキをもって被滅菌体に標識を
施して、その標識の変色によってこれを確認している。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an ink composition for ethylene oxide sterilization marking. This ink composition is used as a printing ink or by marking butylene oxide. When sterilization is performed using these sterilization methods, in order to identify whether sterilization has been completed or not, the object to be sterilized is marked with ink that changes color when sterilization conditions are reached, and the color change of the mark indicates that the object has been sterilized. I've confirmed it.

エチレンオキサイドによる滅菌標識用インキ組成物とし
て一般式A−N=N−Bで表わされる色素〔Aはアルキ
ル基が附加されていなない窒素原子を含むピリジン環、
キノリン環、イソキノリン環、トリアゾール環、テトラ
−ゾル環、インダゾール環およびチアジアゾール環の群
より選ばれた複素環式化合物残基−該残基は非解離性置
換基を有することも有しないこともできるー、Bは通常
のカップリング成分を示す〕、芳香族酸の金属塩、およ
び揮発比が常に1以下である有機液体を成分とするエチ
レンオキサイド滅菌標識用インキ組成物が提案され(特
許1,151.1’76 )、効果が認められている。
A dye represented by the general formula AN=N-B as an ink composition for sterilization labeling using ethylene oxide [A is a pyridine ring containing a nitrogen atom to which no alkyl group is added,
Heterocyclic compound residues selected from the group of quinoline, isoquinoline, triazole, tetra-zole, indazole and thiadiazole rings - the residues may or may not have non-dissociable substituents; [Patent No. 1, 151.1'76), the effect has been recognized.

この先行技術のインキ組成物は、滅菌最適相対湿度(3
0〜80%)ではエチレンオキサイド濃度、滅菌温度、
滅菌時間の3要素に支配されて変色し、正確に滅菌され
たことを標識できるが、低湿度の条件においても同じよ
うに変色する。しかし低湿度条件下では細菌がエチレン
オキサイドに対して抵抗性を示し、正確に滅菌の程度を
示さなくなる。例えば相対湿度0%下での滅菌処理にお
いては、インキ組成物中の色素が変色しているにもかか
わらず、実際には滅菌されていない事がおこりうる。本
願のインキ組成物は上記3要素以外に湿度要素も加わっ
て変色する。従って、最適相対湿度条件(30〜80%
)下では先行技術と同様な変色性を示すが、相対湿度3
0%以下では、変色が次第におそくなり、低湿度下での
菌のエチレンオキサイド抵抗性と一致して変色し、エチ
レンオキサイド滅菌に必要なエチレンオキサイド濃度9
時間、温度及び湿度の4要素全部の積を検知することが
可能となり菌の死滅の様子とよりよく一致するようにな
った。本発明で用いられる色素は下記の一般式で表わさ
れる。
This prior art ink composition has a sterile optimum relative humidity (3
0 to 80%), the ethylene oxide concentration, sterilization temperature,
The color changes depending on the three factors of sterilization time, and can be used to indicate that it has been accurately sterilized, but the color changes in the same way under low humidity conditions. However, under low humidity conditions, bacteria become resistant to ethylene oxide and the degree of sterilization is no longer accurately indicated. For example, in sterilization treatment under 0% relative humidity, it may happen that the ink composition is not actually sterilized even though the pigment in the ink composition has changed color. In addition to the above three factors, the ink composition of the present application changes color due to the addition of a humidity factor. Therefore, optimal relative humidity conditions (30-80%
) shows similar discoloration as the prior art, but at a relative humidity of 3
Below 0%, the discoloration gradually becomes slower, consistent with the bacteria's resistance to ethylene oxide under low humidity, and the ethylene oxide concentration 9 required for ethylene oxide sterilization.
It became possible to detect the product of all four factors: time, temperature, and humidity, and it became possible to better match the state of bacterial death. The dye used in the present invention is represented by the following general formula.

〔式中、Aはエチレン残基又は0−フェニレン残基を表
わし、これらは更に置換基として上記一般式に含まれる
色素はきわめて多種多様であるので、エチレンオキサイ
ドガスによ′ る処理前後の発色、滅菌条件の強弱に適
性ある変色の色素を自由に選択することができる。
[In the formula, A represents an ethylene residue or an 0-phenylene residue, and these are further substituents.Since there are a wide variety of dyes included in the above general formula, the color development before and after treatment with ethylene oxide gas , you can freely select a pigment that changes color and is suitable for the intensity of sterilization conditions.

尚、上記の色素以外に調色のため若干の通常の色素を添
加することがある。本発明で用いられるバインダー樹脂
Iとしては、ポリアクリル酸、ポリメタアクリル酸、ア
クリル酸−メタアクリル酸共重合物が例示できる。
In addition to the above-mentioned pigments, some ordinary pigments may be added to adjust the color. Examples of the binder resin I used in the present invention include polyacrylic acid, polymethacrylic acid, and acrylic acid-methacrylic acid copolymer.

系溶M、エチレングリコールモノエチルエーテル、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
ールモノメチルエーテのエチレングリコールモリアルキ
ルエーテル系溶剤、補助溶剤として、ケトン系溶剤、エ
ステル系溶剤ヲ上記アルコール系、セロソルブ系溶剤に
添加することが出来る。本発明ではポリアクリル酸、ポ
リメタアクリル酸又は、アクリル酸−メタアクリル酸共
重合物に加え添加用樹脂として、ロジン、ロジンエステ
ル。
System solution M, ethylene glycol molyalkyl ether solvent of ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, and as an auxiliary solvent, a ketone solvent or an ester solvent may be added to the above alcohol-based or cellosolve-based solvent. I can do it. In the present invention, in addition to polyacrylic acid, polymethacrylic acid, or acrylic acid-methacrylic acid copolymer, rosin and rosin ester are used as additive resins.

ロジン変性マレイン酸樹脂、アルキルフェノマ ール樹脂、ロジン変性フェノール樹脂、ルーイン酸樹脂
、セルロース系のヒドロキシプロピルセルロース、ヒド
ロキシエチルセルロース、エチルセルロース等の通常油
性インキのバインダー樹脂として用いられる樹脂を使用
し、インキ塗膜の硬度を高め、インキ塗膜のベタツキを
なくしたり、印刷適性を改良することが出来るが他の樹
脂の添加は、湿度に対する効果を小さくする傾向がある
Using resins commonly used as binder resins for oil-based inks, such as rosin-modified maleic acid resin, alkylphenomal resin, rosin-modified phenolic resin, ruic acid resin, cellulose-based hydroxypropyl cellulose, hydroxyethyl cellulose, and ethyl cellulose, the ink coating film is Although the addition of other resins can increase the hardness of the ink film, eliminate stickiness of the ink coating, and improve printability, the addition of other resins tends to reduce the effect on humidity.

本発明では有機酸を添加して、前記色素の変色を促進す
ることができる。
In the present invention, an organic acid can be added to promote discoloration of the dye.

ボン酸、ブタンスルホン酸、ブタンジスルホン酸、ベン
ゼンスルホン酸等のスルホン酸。
Sulfonic acids such as bonic acid, butanesulfonic acid, butanedisulfonic acid, and benzenesulfonic acid.

安息香酸、フター弗酸。フェノール、サリチル酸、スル
ホサリチル酸等の芳香族酸があげられる。特にスルホサ
リチル酸ソーダ、サリチル酸亜鉛のように多塩基酸の酸
基の一つ以上が遊離酸、他の一つ以上が塩の形である酸
性塩タイプの多塩基酸が印刷インキとして使用する場合
、印刷面中より昇華することなく印刷物の保存安定性が
よいので効果よく使用できる。又界面活性剤、防腐剤、
防銹剤あるいは香料等通常のインキ組成物に使用する添
加剤を若干使用することができる。
Benzoic acid, hydrofluoric acid. Examples include aromatic acids such as phenol, salicylic acid, and sulfosalicylic acid. In particular, when polybasic acids of the acid salt type, such as sodium sulfosalicylate and zinc salicylate, in which one or more of the acid groups of the polybasic acid is in the form of a free acid and the other one or more are in the form of a salt, are used as printing inks. It can be used effectively because it does not sublimate from the inside of the printed surface and the storage stability of printed matter is good. Also surfactants, preservatives,
Some additives commonly used in ink compositions, such as rustproofing agents or fragrances, can be used.

本発明のインキを製造するにはインキ組成物100重量
部に対して一般式(1)の色素を0.05〜3.0重量
%、(以下重量%を単に%と記す)好ましくは0.1〜
2%ポリアクリル酸、ポリメタアクリル酸、又はアクリ
ル酸−メタアクリル酸共重合物をインキ組成物100部
に対して0.5%〜50%、好ましくは2%〜30%、
極性溶剤をインキ組成物100部に対して30〜98%
、好ましくは50〜95%必要に応じ添加用樹脂θ〜5
0%、有機酸0〜10.0%、その他適宜量のその他の
添加剤を混合する。
To produce the ink of the present invention, the pigment of general formula (1) is added in an amount of 0.05 to 3.0% by weight, preferably 0.05 to 3.0% by weight (hereinafter, % by weight is simply referred to as %), based on 100 parts by weight of the ink composition. 1~
2% polyacrylic acid, polymethacrylic acid, or acrylic acid-methacrylic acid copolymer, based on 100 parts of the ink composition, 0.5% to 50%, preferably 2% to 30%,
30-98% polar solvent based on 100 parts of the ink composition
, preferably 50 to 95%, optionally adding resin θ to 5
0%, organic acid 0-10.0%, and other additives in appropriate amounts.

インキ製造にあたっては、極性溶剤を常温のまま、ある
いは70〜80°Cに加温し、撹拌しつつ他の成分を加
え、均一に完全に溶解した後撹拌を停止すればよい。
In producing ink, the polar solvent may be kept at room temperature or heated to 70 to 80°C, other components may be added while stirring, and stirring may be stopped after uniform and complete dissolution.

次に実施例を第1表に示して本件発明を一層明らかにす
る。実施例はすべて上記の方法に従って調製した。又ポ
リアクリル酸、ポリメタアクリル酸又はアクリル酸−−
メタアクリル酸共重合物と他のバインダー樹脂との効果
を比較するために、実施例と同様の方法により比較例イ
ンキを闘製し、第1表の下部に示した。
Next, Examples are shown in Table 1 to further clarify the present invention. All examples were prepared according to the methods described above. Also polyacrylic acid, polymethacrylic acid or acrylic acid--
In order to compare the effects of the methacrylic acid copolymer and other binder resins, comparative inks were prepared in the same manner as in the examples and are shown at the bottom of Table 1.

各実施例のインキ中に定性濾紙を浸漬又はシルク印刷し
着色乾燥させたものを試験片とし、50℃において密閉
器中に水蒸気の存在下(65%R11)および不存在下
でエチレンオキサイド濃度500■/l (大同酸素側
製、グイサイドLS)下で 1時間および2時間放置し
、試験片の変色を日本重色工業側製、色差直続デジタル
測色色差計ND−504AA型にて測定した。その結果
および65%RHと0%ti11のときの変色の比を第
2表に示した。この数値より本件発明のインキ組成物は
水蒸気が存在しないと変色速度が遅くなることが認めら
れる。尚、上記の湿度65%2時間エチレンオキサイド
にさらす条件では生物学的検査により通常の被滅菌体で
滅菌が完了する条件であることを別途確認した。
Qualitative filter paper was immersed or silk-printed in the ink of each example, colored and dried, and used as a test piece. At 50°C, in a closed container in the presence of water vapor (65% R11) and in the absence, the ethylene oxide concentration was 500. The specimen was left for 1 and 2 hours under ■/l (Guiside LS, manufactured by Daido Oxygen Co., Ltd.), and the discoloration of the test piece was measured using a color difference direct-connection digital colorimeter, model ND-504AA, manufactured by Nihon Heavy Industries. . The results and the ratio of discoloration at 65% RH and 0% ti11 are shown in Table 2. From this value, it is recognized that the ink composition of the present invention exhibits a slow discoloration rate in the absence of water vapor. It was separately confirmed by biological testing that the above conditions of exposure to ethylene oxide at 65% humidity for 2 hours were sufficient to complete sterilization in normal objects to be sterilized.

Claims (1)

【特許請求の範囲】 一般式 で示される色素 〔式中、Aはエチレン残基又は0−フェニレン残基を表
わし、これらは更に置換基としてヒドロキシ低級アルキ
ル基である。〕 ポリアクリル酸、ポリメタアクリル酸およびアクリル酸
−メタアクリル酸共重合物よりなる群より選ばれた少く
とも1種の樹脂、極性溶剤よりなるエチレンオキサイド
滅菌標識用インキ組成物。
[Scope of Claims] A dye represented by the general formula [wherein A represents an ethylene residue or an 0-phenylene residue, which is further a hydroxy lower alkyl group as a substituent. ] An ink composition for ethylene oxide sterilization markings comprising at least one resin selected from the group consisting of polyacrylic acid, polymethacrylic acid, and acrylic acid-methacrylic acid copolymers, and a polar solvent.
JP59099292A 1984-05-16 1984-05-16 Ink composition for marking sterilization with ethylene oxide Pending JPS60243173A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59099292A JPS60243173A (en) 1984-05-16 1984-05-16 Ink composition for marking sterilization with ethylene oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59099292A JPS60243173A (en) 1984-05-16 1984-05-16 Ink composition for marking sterilization with ethylene oxide

Publications (1)

Publication Number Publication Date
JPS60243173A true JPS60243173A (en) 1985-12-03

Family

ID=14243562

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59099292A Pending JPS60243173A (en) 1984-05-16 1984-05-16 Ink composition for marking sterilization with ethylene oxide

Country Status (1)

Country Link
JP (1) JPS60243173A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5028647A (en) * 1986-10-24 1991-07-02 Allied-Signal Inc. Polyester composition containing an ester of an ethoxylated aromatic alcohol
US5258065A (en) * 1991-06-24 1993-11-02 Sakura Color Products Corporation Ink composition for indicating the progress of sterilization with ethylene oxide

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5210043A (en) * 1975-07-14 1977-01-26 Mitsubishi Electric Corp Central processing unit with memory display
JPS53106204A (en) * 1977-02-28 1978-09-16 Toppan Printing Co Ltd Ink composition
JPS5740869A (en) * 1980-08-25 1982-03-06 Seiko Instr & Electronics Ltd Non-aqueous electrolyte battery

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5210043A (en) * 1975-07-14 1977-01-26 Mitsubishi Electric Corp Central processing unit with memory display
JPS53106204A (en) * 1977-02-28 1978-09-16 Toppan Printing Co Ltd Ink composition
JPS5740869A (en) * 1980-08-25 1982-03-06 Seiko Instr & Electronics Ltd Non-aqueous electrolyte battery

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5028647A (en) * 1986-10-24 1991-07-02 Allied-Signal Inc. Polyester composition containing an ester of an ethoxylated aromatic alcohol
US5258065A (en) * 1991-06-24 1993-11-02 Sakura Color Products Corporation Ink composition for indicating the progress of sterilization with ethylene oxide

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