JPH02311404A - Germicide composition for industry - Google Patents

Germicide composition for industry

Info

Publication number
JPH02311404A
JPH02311404A JP12878289A JP12878289A JPH02311404A JP H02311404 A JPH02311404 A JP H02311404A JP 12878289 A JP12878289 A JP 12878289A JP 12878289 A JP12878289 A JP 12878289A JP H02311404 A JPH02311404 A JP H02311404A
Authority
JP
Japan
Prior art keywords
paraclox
composition
ddo
composition containing
dbnpa
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
JP12878289A
Other languages
Japanese (ja)
Inventor
Yasuharu Nobata
野畑 靖治
Isao Kato
功 加藤
Akira Togo
藤後 章
Noriko Tanimura
谷村 徳子
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.)
HAKUTOU KAGAKU KK
Original Assignee
HAKUTOU KAGAKU KK
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 HAKUTOU KAGAKU KK filed Critical HAKUTOU KAGAKU KK
Priority to JP12878289A priority Critical patent/JPH02311404A/en
Publication of JPH02311404A publication Critical patent/JPH02311404A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain the synergistic subject composition containing PARACLOX and DBNPA or DDO as active ingredients and especially used in drain system. CONSTITUTION:The germicidal composition containing 4-hydroxyphenyl-alpha- ketoacetohydroxium acid chloride (PARACLOX) expressed by the formula, dibromonitorylopropionic amide(DBNPA) or 4,5-dichloro-1,2-dithiol-3-one(DDO) at a weight ratio of 9:1 to 1:9. The composition containing 5 to 25wt.% active ingredients in final composition containing a solvent and the dispersed agent is added to water system to be treated in an amount of 2 to 400ppm (2 to 20ppm, in circulating water for paper making).

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、産業、特に用排水系に用いる相乗効果的な殺
菌組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to synergistic disinfectant compositions for use in industry, particularly in industrial and wastewater systems.

〔従来の技術〕[Conventional technology]

従来より、工業用冷却水、パルプや紙などの製造に用い
られる水、いわゆるプロセス水や白水などの用排水系は
、種々の細菌、カビあるいは酵母などの微生物の侵害を
受け、熱交換器の閉塞や紙切れなどの問題を引き起して
いる。これら用排水系の微生物による侵害を防除するた
めに多数の殺画側、特に非金属系有機殺菌剤が用いられ
ている。
Traditionally, industrial cooling water, water used in the manufacture of pulp and paper, so-called process water, and wastewater systems have been attacked by microorganisms such as various bacteria, molds, and yeasts, resulting in damage to heat exchangers. This is causing problems such as blockages and paper cuts. A number of biocides, particularly non-metallic organic biocides, are used to control microbial infestation of these drainage systems.

例えば特公昭52−14294号、同53−5375号
および同62−23721号の各公報ならびに特開昭5
1−82723号、同54−132230号、同54−
135223号、同60−1105号および同61−9
1108号の各公報には、種々のスライムコントロール
剤、抗微生物、工業用殺菌剤およびそれらの2以上を含
む組成物ならびにそれらを用いる用排水系のスライムコ
ントロール法等が開示されている。それらに用いる薬剤
はそれぞれ一長一短はあるものの、安全性・毒性・発泡
性・pH依存性・腐食性・水溶性・安定性・費用効果・
効果の持続性等に関しなんらかの欠点を有するために、
工業用殺菌剤として満足すべきものは未開発の状態にあ
る。
For example, Japanese Patent Publications No. 52-14294, No. 53-5375, and No. 62-23721;
No. 1-82723, No. 54-132230, No. 54-
No. 135223, No. 60-1105 and No. 61-9
Each publication of No. 1108 discloses various slime control agents, antimicrobials, industrial disinfectants, compositions containing two or more of these, and slime control methods for drainage systems using them. Although the chemicals used for these have their advantages and disadvantages, they are safe, toxic, foaming, pH-dependent, corrosive, water-soluble, stable, cost-effective,
Because it has some drawbacks regarding the sustainability of the effect, etc.
A satisfactory industrial disinfectant remains undeveloped.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

プ工業の用排水系に卓効があり安全性・安定性・持続性
に富む殺菌組成物を探究したところ、特定の2成分系組
成物が広汎な2成分配合範囲に亘って顕著な相乗的殺菌
効果を発揮することを見出し、本発明を完成するに至っ
た。
When we searched for a safe, stable, and long-lasting disinfectant composition that is highly effective for industrial wastewater systems, we found that a specific two-component composition showed remarkable synergistic effects over a wide range of two-component combinations. They discovered that it exhibits a bactericidal effect and completed the present invention.

〔問題点を解決するための手段〕[Means for solving problems]

本発明の産業用殺菌組成物は、 によって表わされる4−ヒドロキシフェニール−α−ケ
トアセトヒドロキシウム酸クりライド(PARACLO
X)とジブロムニトリロプロピオンアミド(D B N
 P A)もしくは4.5−ジクロール−1,2−ジオ
チール−3−オン(D D O)とを有効成分として構
成され、同じく水系の殺菌方法はPARACLOXとD
BNPAもしくはDDOとを有効成分とする殺菌組成物
を該水系に適用することによって構成される。
The industrial fungicidal composition of the present invention comprises 4-hydroxyphenyl-α-ketoacetohydroxyum acid chloride (PARACLO) represented by
X) and dibromnitrilopropionamide (D B N
P A) or 4,5-dichlor-1,2-diothyl-3-one (D DO) as an active ingredient, and the water-based sterilization method is PARACLOX and D
It is constructed by applying a disinfectant composition containing BNPA or DDO as an active ingredient to the aqueous system.

本発明の組成物は、それぞれ単独の使用では満足する殺
菌効果を得るには比較的多量の添加を必要とするに対し
て、両者を組み合わせると、著しく少量で殺菌効果を発
揮し、かつ広範囲の有害微生物の殺菌に有効である。
The composition of the present invention requires a relatively large amount to be added to obtain a satisfactory bactericidal effect when used alone, but when both are combined, it exhibits a bactericidal effect with a significantly small amount and has a wide range of effects. Effective in killing harmful microorganisms.

本発明の組成物は、液体形で使用される。好ましくは貯
蔵安定な組成物を与える親水性有機溶媒が活性分を溶解
するために使用される。そのような溶媒の例は、アミド
例えばジメチルホルムアミド、グリコール例えばエチレ
ングリコール、プロピレングリコール、ブチルグリコー
ル、ポリエチレングリコール、グリコールエーテル例え
ばジエチレングリコールモノメチルエーテル又はエチレ
ングリコールブチルエーテルがあり、好ましくはポリエ
チレングリコールの分子ji200程度のものがよい。
The composition of the invention is used in liquid form. Preferably a hydrophilic organic solvent that provides a storage stable composition is used to dissolve the active ingredient. Examples of such solvents are amides such as dimethylformamide, glycols such as ethylene glycol, propylene glycol, butyl glycol, polyethylene glycol, glycol ethers such as diethylene glycol monomethyl ether or ethylene glycol butyl ether, preferably molecules of polyethylene glycol of the order of ji200. Good.

PARACLOXとDDOとの組成物を水性系に使用す
る場合、組成物の系への分布を容易にしかつこれを改善
するために、分散剤の添加が必要である。
When the composition of PARACLOX and DDO is used in an aqueous system, the addition of a dispersant is necessary to facilitate and improve the distribution of the composition into the system.

好適な分散剤は、陽イオン性、陰イオン性、非イオン性
又は両性の界面活゛性剤であり、特に好ましくは非イオ
ン性及び陰イオン性の界面活性剤である。適当な非イオ
ン活性剤の例は、高級アルコールエチレンオキシド(E
O)−付加物、アルキルフェノールE〇−付加物、プロ
ピレンオキシド−EO付加物、及びポリグリコールエー
テル及び、又はエステルである。陰イオン界面活性剤の
例は、アルキルベンゼンスルホネート、2級アルカンス
ルホネート、オレフィンスルホネート、脂肪族アルコー
ルサルフェート及び脂肪族アルコールエーテルサルフェ
ートである。
Suitable dispersants are cationic, anionic, nonionic or amphoteric surfactants, particularly preferably nonionic and anionic surfactants. An example of a suitable nonionic activator is the higher alcohol ethylene oxide (E
O)-adducts, alkylphenol E〇-adducts, propylene oxide-EO adducts, and polyglycol ethers and/or esters. Examples of anionic surfactants are alkylbenzene sulfonates, secondary alkanesulfonates, olefin sulfonates, fatty alcohol sulfates and fatty alcohol ether sulfates.

本発明の組成物中の活性分の配合比率は、PARACL
OX : DBNPA及びPARACLOX:DDOの
各につき重量比で9:1〜1〜9の範囲内にあるとき良
好な効果が得られた。
The blending ratio of active ingredients in the composition of the present invention is PARACL
Good effects were obtained when the weight ratio of OX:DBNPA and PARACLOX:DDO was within the range of 9:1 to 1 to 9.

溶媒、分散剤を含む最終組成物中の有効成分の含有量は
、約5〜25重量%であるが、約50重量%までの含量
が可能である。
The content of active ingredient in the final composition, including solvents and dispersants, is about 5-25% by weight, but contents up to about 50% by weight are possible.

本発明の組成物は、処理ずべき水系に約2〜400pp
mの量で添加されるが、一般に製紙循環水では2〜20
ppmの添加量で十分である。
The composition of the present invention can be added to the aqueous system to be treated in an amount of about 2 to 400 pp.
It is generally added in an amount of 2 to 20 m for papermaking circulating water.
An addition amount of ppm is sufficient.

以下実施例によって本発明をさらに詳しく説明するが、
これらによって本発明の範囲が何ら制限されるものでは
ない。
The present invention will be explained in more detail with reference to Examples below.
These do not limit the scope of the present invention in any way.

〔実施例1〕 4−ヒドロキシフェニール−α−ケトアセトヒドロキシ
ウム酸クりライド(PARACLOX)の20%重量ポ
リエチレングリコール200、ジブロムニトリロプロピ
オンアミド(D B N P A)の20%重量ポリエ
チレングリコール200及び両者の混合比率9:1〜1
:9により配合した有効成分濃度20%重量ポリエチレ
ングリコール200を調製した。
[Example 1] 20% weight polyethylene glycol 200 of 4-hydroxyphenyl-α-ketoacetohydroxyum acid chloride (PARACLOX), 20% weight polyethylene glycol 200 of dibromnitrilopropionamide (DBNPA) and a mixing ratio of both 9:1 to 1
Polyethylene glycol 200 with an active ingredient concentration of 20% by weight was prepared according to the following method.

使用に際してはそのまま水で希釈して使用した。When used, it was diluted with water and used as is.

ついで製紙工程中の有害微生物に対する殺菌効果を試験
するために、上質紙を製造している抄紙系から採取した
微生物デポジットを変性ワックスマン培地に植えつぎ3
2℃4日間培養した後、コロニーの色、形から優先菌種
と思われる3種のバクテリアを選び、これらをそれぞれ
ブイヨン液体培地でさらに培養した菌液を用いて、殺菌
テストを行った。
Next, in order to test the bactericidal effect against harmful microorganisms during the paper manufacturing process, microbial deposits collected from a papermaking system that produces high-quality paper were planted in a modified Waxman medium.
After culturing at 2°C for 4 days, three types of bacteria considered to be the preferential bacterial species were selected based on the color and shape of the colonies, and a bactericidal test was performed using the bacterial liquid that was further cultured in a broth liquid medium.

菌種の同定は、各種生理試験を行いS、 T、  Co
 w a nの分類表に従い同定した。これらは一般に
製紙工程で見られるFfl avobac t e r
 ium、Pseudomonas、Al cap i
genesであった。
To identify the bacterial species, various physiological tests were performed to identify S, T, and Co.
It was identified according to the classification table of wan. These are Ffl avocados commonly found in the papermaking process.
ium, Pseudomonas, Al cap i
It was genes.

滅菌白水中に、予め培養した菌液をとり、これに所定量
の殺菌組成物を添加して、30分間32℃で振とう後、
変性ワックスマン培地に接種して、32℃、4日間培養
液の全菌数がゼロになる濃度を求めて、最少殺菌濃度と
した。結果を表−1に示す。
A pre-cultured bacterial solution was taken in sterile white water, a predetermined amount of the sterilizing composition was added thereto, and after shaking at 32°C for 30 minutes,
A modified Waxman medium was inoculated, and the concentration at which the total number of bacteria in the culture solution became zero at 32° C. for 4 days was determined, and this was determined as the minimum bactericidal concentration. The results are shown in Table-1.

菌種 PL:Fj 1vobacteriumPS: 
Pseudomonas AL:^J c al igenes 上記の結果から明らかな様に、PARACLOXとDB
NPAとの組成物はそれぞれ単独に比べて著しく少い添
加量で殺菌する事が判る。
Bacterial species PL:Fj 1vobacteriumPS:
Pseudomonas AL:^J cal igenes As is clear from the above results, PARACLOX and DB
It can be seen that the composition with NPA sterilizes with a significantly smaller amount added than each alone.

〔実施例2〕 PARACLOXの25%重量ポリエチレングリコール
200およびDDOの25%重量ポリエチレングリコー
ル200を両者の混合比率9:1〜1:9で配合したも
のにHLB14のポリエチV レンゲリコールアルキZエノールを10%重量重筋して
、有効成分濃度20%重量ポリエチレングリコール20
0を調製した。
[Example 2] 25% weight polyethylene glycol 200 of PARACLOX and 25% weight polyethylene glycol 200 of DDO were blended at a mixing ratio of 9:1 to 1:9, and 10% of polyethylene glycol alkyl Z enol of HLB 14 was added. % weight, active ingredient concentration 20% weight polyethylene glycol 20
0 was prepared.

使用に際してはそのまま水で希釈して使用した。When used, it was diluted with water and used as is.

ついで実施例1と同様の手法により製紙工程中の有害微
生物に対する殺菌効果を試験した。ただし殺菌剤組成物
としては上記のとおり調製したPARACLOX/DD
O組成物を用いた。結果を表−2に示す。
Then, using the same method as in Example 1, the bactericidal effect against harmful microorganisms during the paper manufacturing process was tested. However, as a fungicide composition, PARACLOX/DD prepared as above
O composition was used. The results are shown in Table-2.

表−2 菌種 PL:Pj !vobacterlumPs:P
seUdO1fiOnaS AL:^JeIJIgenes 上記の結果から明らかな様に、PARACLOXとDD
Oとの組成物は、それぞれ単独に比べて著しく少い添加
量で殺菌する事が判る。
Table-2 Bacterial species PL:Pj! vobacterlumPs:P
seUdO1fiOnaS AL: ^JeIJIgenes As is clear from the above results, PARACLOX and DD
It can be seen that the composition with O can be sterilized with a significantly smaller amount added than each alone.

〔発明の効果〕〔Effect of the invention〕

Claims (1)

【特許請求の範囲】 1、式▲数式、化学式、表等があります▼ によって表わされる4−ヒドロキシフェニール−α−ケ
トアセトヒドロキシゥム酸クロライド(PARACLO
X)とジブロムニトリロプロピオンアミド(DBNPA
)とを有効成分として含有することを特徴とする産業用
殺菌組成物。 2、PARACLOX:DBNPAの重量比が9:1な
いし1:9の範囲内にある第1請求項記載の組成物。 3、式▲数式、化学式、表等があります▼ によって表わされる4−ヒドロキシフェニール−α−ケ
トアセトヒドロキシゥム酸クロライド(PARACLO
X)と4,5−ジクロール−1,2−ジオチール−3−
オン(DDO)とを有効成分として含有することを特徴
とする産業用殺菌組成物。 4、PARACLOX:DDOの重量比が9:1ないし
1:9の範囲内にある第1請求項記載の組成物。 5、第1ないし第4請求項のいずれかに記載の組成物を
用いることを特徴とする水系の殺菌方法。
[Claims] 1. 4-hydroxyphenyl-α-ketoacetohydroxyum acid chloride (PARACLO
X) and dibromnitrilopropionamide (DBNPA
) as an active ingredient. 2. The composition according to claim 1, wherein the weight ratio of PARACLOX:DBNPA is in the range of 9:1 to 1:9. 3. 4-Hydroxyphenyl-α-ketoacetohydroxyum acid chloride (PARACLO
X) and 4,5-dichlor-1,2-diothyl-3-
1. An industrial sterilizing composition characterized by containing DDO (DDO) as an active ingredient. 4. The composition according to claim 1, wherein the weight ratio of PARACLOX:DDO is in the range of 9:1 to 1:9. 5. A water-based sterilization method characterized by using the composition according to any one of claims 1 to 4.
JP12878289A 1989-05-24 1989-05-24 Germicide composition for industry Pending JPH02311404A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12878289A JPH02311404A (en) 1989-05-24 1989-05-24 Germicide composition for industry

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12878289A JPH02311404A (en) 1989-05-24 1989-05-24 Germicide composition for industry

Publications (1)

Publication Number Publication Date
JPH02311404A true JPH02311404A (en) 1990-12-27

Family

ID=14993328

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12878289A Pending JPH02311404A (en) 1989-05-24 1989-05-24 Germicide composition for industry

Country Status (1)

Country Link
JP (1) JPH02311404A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL9500377A (en) * 1994-03-26 1995-11-01 Benckiser Knapsack Ladenburg Method and means for oxidative bleaching of wood materials and for removing ink from old paper.
ITNA20130042A1 (en) * 2013-07-24 2015-01-25 Celko Chemical S R L POLYVALENT ADDITIVES FOR FOOD WATERS OF REVERSE OSMOSIS PLANTS

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL9500377A (en) * 1994-03-26 1995-11-01 Benckiser Knapsack Ladenburg Method and means for oxidative bleaching of wood materials and for removing ink from old paper.
ITNA20130042A1 (en) * 2013-07-24 2015-01-25 Celko Chemical S R L POLYVALENT ADDITIVES FOR FOOD WATERS OF REVERSE OSMOSIS PLANTS

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