JPH06305917A - Industrial fungicidal composition - Google Patents

Industrial fungicidal composition

Info

Publication number
JPH06305917A
JPH06305917A JP5117912A JP11791293A JPH06305917A JP H06305917 A JPH06305917 A JP H06305917A JP 5117912 A JP5117912 A JP 5117912A JP 11791293 A JP11791293 A JP 11791293A JP H06305917 A JPH06305917 A JP H06305917A
Authority
JP
Japan
Prior art keywords
fungicidal composition
industrial
test example
present
latex
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
JP5117912A
Other languages
Japanese (ja)
Other versions
JP3252015B2 (en
Inventor
Hitoshi Egawa
均 江川
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.)
Shinto Paint Co Ltd
Original Assignee
Shinto Paint 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 Shinto Paint Co Ltd filed Critical Shinto Paint Co Ltd
Priority to JP11791293A priority Critical patent/JP3252015B2/en
Publication of JPH06305917A publication Critical patent/JPH06305917A/en
Application granted granted Critical
Publication of JP3252015B2 publication Critical patent/JP3252015B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To provide an industrial fungicidal composition capable of facilitating the hitherto difficult suppression of microbial proliferation in an aquatic system and exhibiting effective action even on a CMT-resistant microorganism. CONSTITUTION:The industrial fungicidal composition contains methylene bisthiocyanate and 1,2-benzisothiazolin-3-one as active components.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、接着剤、塗料、紙、繊
維および建材等の諸工業分野において利用されている合
成樹脂ラテックス等の含水工業原料および製品が微生物
汚染を受けることを防止するための工業用殺菌組成物に
関するものである。
FIELD OF THE INVENTION The present invention prevents hydrated industrial raw materials and products such as synthetic resin latexes used in various industrial fields such as adhesives, paints, papers, fibers and construction materials from being subjected to microbial contamination. The present invention relates to an industrial sterilizing composition.

【0002】[0002]

【従来の技術および発明が解決しようとする課題】近
年、化学工業の発展にともない、合成樹脂ラテックス、
コーテイングカラー、デンプンスラリーなどの含水工業
原料における微生物対策が重要となっている。 この微
生物障害を避けるために、種々の工業用殺菌剤が使用さ
れているが、効力、安定性共に有効な5−クロロ−2−
メチル−4−イソチアゾリン−3−オン(以下CMTと
略す)を単独で、または他の殺菌剤との合剤として接着
剤、塗料、紙、繊維、及び建材等の諸工業分野において
利用されている合成樹脂ラテックス等の含水工業原料及
び製品の腐敗を防止するために添加されることが非常に
多い。しかし同一の成分の使用では腐敗を防止する対象
となる微生物に耐性がつくなどの理由で充分な効力が得
られず、しばしば殺菌剤の使用量が増え、コストも高く
なることが多く問題があった。また、メチレンビスチオ
シアネートは抗菌力、静菌力にすぐれた殺菌剤として知
られているが、単独に適用した場合には安定性が問題と
なり効力が持続しないという問題があった。
2. Description of the Related Art In recent years, with the development of the chemical industry, synthetic resin latex,
Microbial countermeasures for water-containing industrial raw materials such as coating color and starch slurry have become important. In order to avoid this microbial damage, various industrial bactericides are used, but 5-chloro-2-, which is effective in terms of both efficacy and stability, is used.
Methyl-4-isothiazolin-3-one (hereinafter abbreviated as CMT) is used in various industrial fields such as adhesives, paints, papers, fibers, and building materials alone or as a mixture with other fungicides. Very often it is added to prevent decomposition of water-containing industrial raw materials such as synthetic resin latex and products. However, the use of the same component does not provide sufficient efficacy because it is resistant to microorganisms that are intended to prevent spoilage, and often the amount of bactericide used increases and the cost often increases. It was Further, methylenebisthiocyanate is known as a bactericide having excellent antibacterial activity and bacteriostatic activity, but when used alone, there is a problem that stability becomes a problem and the efficacy does not last.

【0003】[0003]

【課題を解決するための手段】本発明者はその抗菌力を
補う為に鋭意研究を重ねた結果、メチレンビスチオシア
ネートに1、2−ベンズイソチアゾリン−3−オンを組
合せて使用した場合CMT耐性菌に対しても有効で、ま
たメチレンビスチオシアネート単独の使用では充分な防
腐効力を示さない長期間においても有効な効力を有する
ことを見い出した。すなわち本発明はメチレンビスチオ
シアネートと1、2−ベンズイソチアゾリン−3−オン
を有効成分として含有することを特徴とする工業用殺菌
組成物である。
Means for Solving the Problems As a result of intensive studies to supplement the antibacterial activity of the present inventor, the present inventor has found that CMT-resistant bacteria when methylenebisthiocyanate is used in combination with 1,2-benzisothiazolin-3-one. It has been found that it is also effective against the above-mentioned effects, and that it has an effective effect even for a long period of time when the use of methylenebisthiocyanate alone does not show sufficient antiseptic effect. That is, the present invention is an industrial sterilizing composition containing methylenebisthiocyanate and 1,2-benzisothiazolin-3-one as active ingredients.

【0004】本発明のメチレンビスチオシアネートと
1、2−ベンズイソチアゾリン−3−オンの割合は任意
であるが、重量比で10:1〜1:10好ましくは4:
1〜1:4の範囲が望ましい。以下の実施例によって本
発明をさらに詳細に説明する。
The ratio of methylenebisthiocyanate to 1,2-benzisothiazolin-3-one of the present invention is arbitrary, but the weight ratio is 10: 1 to 1:10, preferably 4 :.
The range of 1 to 1: 4 is desirable. The present invention will be described in more detail by the following examples.

【0005】[0005]

【実施例】次に本発明の実施例および比較例をあげて説
明するが、本発明はこれらに限定されるものではない。
下表に示した配合比率はすべて重量%である。また、各
実施例の殺菌組成物は各実施例に示す各成分をそれぞれ
示す割合で常温において通常の撹拌によって調製した。
EXAMPLES Examples and comparative examples of the present invention will be described below, but the present invention is not limited thereto.
All the compounding ratios shown in the table below are weight%. The bactericidal composition of each example was prepared by ordinary stirring at room temperature in the proportions shown for each component shown in each example.

【0006】実施例1〜3 表1に示す抗菌剤組成物を調製し、試験例1、試験例
2、試験例3、試験例4により、その性能を調べた。
Examples 1 to 3 The antibacterial agent compositions shown in Table 1 were prepared and their performances were examined by Test Example 1, Test Example 2, Test Example 3 and Test Example 4.

【0007】[0007]

【表1】 [Table 1]

【0008】比較例1〜3 表2に示す抗菌剤組成物を調製し、試験例1、試験例
2、試験例3、試験例4により、その性能を調べた。
Comparative Examples 1 to 3 The antibacterial agent compositions shown in Table 2 were prepared and their performances were examined by Test Example 1, Test Example 2, Test Example 3 and Test Example 4.

【0009】[0009]

【表2】 [Table 2]

【0010】*:5−クロロ−2−メチル−イソチアゾ
リン−3−オン 10%エチレングリコール溶液(市川
合成株式会社製)
*: 5-chloro-2-methyl-isothiazolin-3-one 10% ethylene glycol solution (manufactured by Ichikawa Gosei Co., Ltd.)

【0011】試験例1 ラテックスの防腐 スチレン・ブタジエンラテックス(pH7.0)を採取
し、滅菌ポリプロピレン瓶に30g分注し薬剤を所定量
添加した。これを密閉静置条件で30℃で培養し、BH
I寒天平板法によって経時的な生菌数を測定し、防腐効
果を判定した。下記の判定基準をもって判定した。な
お、試験例2〜4の結果についても同様の基準で表示し
た。 −: 102 未満 +: 102 以上104 未満 ++: 104 以上106 未満 +++: 106 以上107 未満 ++++: 107 以上 この結果を表3に示す。表3から明らかなように、本発
明の殺菌組成物はラテックスに対して、各々の単独の製
剤よりも高い防腐効力を持つことがわかる。
Test Example 1 Preservation of Latex Styrene-butadiene latex (pH 7.0) was sampled and dispensed into a sterile polypropylene bottle in an amount of 30 g, and a predetermined amount of the drug was added. This is cultivated at 30 ° C in a closed static condition, and BH
The preservative effect was determined by measuring the viable cell count over time by the I agar plate method. It judged by the following judgment criteria. The results of Test Examples 2 to 4 are also shown based on the same criteria. −: Less than 10 2 +: 10 2 or more and less than 10 4 ++: 10 4 or more and less than 10 6 +++: 10 6 or more and less than 10 7 ++++: 10 7 or more The results are shown in Table 3. As is clear from Table 3, the bactericidal composition of the present invention has a higher antiseptic effect on latex than the individual preparations.

【0012】[0012]

【表3】 [Table 3]

【0013】試験例2 ラテックスの防腐 スチレン・ブタジエンラテックス(pH7.0)を採取
し、滅菌ポリプロピレン瓶に30g分注し薬剤を所定量
添加した。これを密閉静置条件で30℃で培養し、BH
I寒天平板法によって経時的な生菌数を測定して防腐効
果を判定した。また腐敗を促進させるために低濃度のC
MTを接触させ腐敗させたラテックスを7日毎に接種し
た。この結果を表4に示す。表4から明らかなように、
本発明の殺菌組成物はCMT耐性菌による腐敗ラテック
スに対しても有効な効力を示した。
Test Example 2 Preservation of Latex Styrene-butadiene latex (pH 7.0) was sampled and dispensed into a sterilized polypropylene bottle in an amount of 30 g, and a predetermined amount of the drug was added. This is cultivated at 30 ° C in a closed static condition, and BH
The preservative effect was determined by measuring the viable cell count over time by the I agar plate method. Also, a low concentration of C is added to promote decay.
MT was contacted and putrefaction latex was inoculated every 7 days. The results are shown in Table 4. As is clear from Table 4,
The bactericidal composition of the present invention showed effective efficacy against spoiled latex caused by CMT-resistant bacteria.

【0014】[0014]

【表4】 [Table 4]

【0015】試験例3 塗工紙のコーティングカラーの
防腐 酢酸ビニルエマルジョン(pH5.1)を採取し、滅菌
ポリプロピレン瓶に30g分注し薬剤を所定量添加し
た。これを密閉静置条件で30℃で培養し、BHI寒天
平板法によって経時的な生菌数を測定し、防腐効果を判
定した。この結果を表5に示す。表5から明らかなよう
に、本発明の殺菌組成物はコーティングカラーに対し
て、各々の単独の製剤よりも高い防腐効力を持つことが
わかる。
Test Example 3 Antiseptic coating color of coated paper Vinyl acetate emulsion (pH 5.1) was sampled and dispensed into a sterile polypropylene bottle in an amount of 30 g, and a predetermined amount of the drug was added. This was cultivated at 30 ° C. in a closed static condition, and the viable cell count over time was measured by the BHI agar plate method to determine the antiseptic effect. The results are shown in Table 5. As is apparent from Table 5, the bactericidal composition of the present invention has a higher antiseptic effect on the coating color than the individual formulations.

【0016】[0016]

【表5】 [Table 5]

【0017】試験例4 デンプンスラリーの防腐 カチオン化タピオカデンプンの10%スラリー(pH
6.2)を調製し、滅菌ポリプロピレン瓶に30g分注
し薬剤を所定量添加した。これを密閉静置条件で30℃
で培養し、BHI寒天平板法によって経時的な生菌数を
測定し、防腐効果を判定した。この結果を表6に示し
た。表6から明らかなように、本発明の殺菌組成物はデ
ンプンスラリーに対して、各々の単独の製剤よりも高い
防腐効力を持つことがわかる。
Test Example 4 Preservation of Starch Slurry 10% slurry of cationized tapioca starch (pH
6.2) was prepared, 30 g was dispensed into a sterile polypropylene bottle, and a predetermined amount of the drug was added. This is closed at 30 ° C under static conditions.
After culturing in, the number of viable cells over time was measured by the BHI agar plate method to determine the antiseptic effect. The results are shown in Table 6. As is clear from Table 6, the bactericidal composition of the present invention has a higher antiseptic effect on starch slurries than each of the single formulations.

【0018】[0018]

【表6】 [Table 6]

【0019】[0019]

【発明の効果】本発明を適用した場合、いままで困難だ
った水系の微生物の増殖を抑えることが容易になり、ま
たCMT耐性菌に対しても有効な効力を示す。
INDUSTRIAL APPLICABILITY When the present invention is applied, it becomes easy to suppress the growth of water-based microorganisms, which has been difficult until now, and it also exhibits effective efficacy against CMT-resistant bacteria.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 メチレンビスチオシアネートと1、2−
ベンズイソチアゾリン−3−オンを有効成分として含有
することを特徴とする工業用殺菌組成物。
1. Methylenebisthiocyanate and 1,2-
An industrial sterilizing composition comprising benzisothiazolin-3-one as an active ingredient.
JP11791293A 1993-04-20 1993-04-20 Industrial germicidal composition Expired - Fee Related JP3252015B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11791293A JP3252015B2 (en) 1993-04-20 1993-04-20 Industrial germicidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11791293A JP3252015B2 (en) 1993-04-20 1993-04-20 Industrial germicidal composition

Publications (2)

Publication Number Publication Date
JPH06305917A true JPH06305917A (en) 1994-11-01
JP3252015B2 JP3252015B2 (en) 2002-01-28

Family

ID=14723258

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11791293A Expired - Fee Related JP3252015B2 (en) 1993-04-20 1993-04-20 Industrial germicidal composition

Country Status (1)

Country Link
JP (1) JP3252015B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006328007A (en) * 2005-05-27 2006-12-07 Shinto Fine Co Ltd Industrial anti-microbial composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006328007A (en) * 2005-05-27 2006-12-07 Shinto Fine Co Ltd Industrial anti-microbial composition

Also Published As

Publication number Publication date
JP3252015B2 (en) 2002-01-28

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