JPH05155719A - Release of slime - Google Patents

Release of slime

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Publication number
JPH05155719A
JPH05155719A JP32050391A JP32050391A JPH05155719A JP H05155719 A JPH05155719 A JP H05155719A JP 32050391 A JP32050391 A JP 32050391A JP 32050391 A JP32050391 A JP 32050391A JP H05155719 A JPH05155719 A JP H05155719A
Authority
JP
Japan
Prior art keywords
slime
isothiazolone
compound
water system
aqueous system
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
JP32050391A
Other languages
Japanese (ja)
Other versions
JP2565043B2 (en
Inventor
Satoshi Kashiwagi
聡 柏木
Yasushi Murano
靖 村野
Takashi Kawamura
高 川村
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.)
Kurita Water Industries Ltd
Original Assignee
Kurita Water Industries 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 Kurita Water Industries Ltd filed Critical Kurita Water Industries Ltd
Priority to JP3320503A priority Critical patent/JP2565043B2/en
Publication of JPH05155719A publication Critical patent/JPH05155719A/en
Application granted granted Critical
Publication of JP2565043B2 publication Critical patent/JP2565043B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To readily and efficiently release slime adhering to an aqueous system with industrial advantage. CONSTITUTION:Slime adhering to an aqueous system is released by intermittently adding an isothiazolone-based compound to the slime-adhering aqueous system. The isothiazolone-based compound exhibits a denaturation and decoloration effect on the slime and the viscosity of the polysaccharide can be removed. The already adhered, slime, therefore, can efficiently be released by intermittently adding the isothiazolone-based compound to the aqueous system.

Description

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

【0001】[0001]

【産業上の利用分野】本発明はスライム剥離方法に係
り、特に、冷却水系に付着しているスライムを、容易か
つ効率的に、工業的に有利に剥離する方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a slime stripping method, and more particularly to a method for stripping slime adhering to a cooling water system easily, efficiently and industrially advantageously.

【0002】[0002]

【従来の技術】各種工場プラントの冷却水系では、細
菌、糸状菌、藻類等から構成されるスライムが系内に発
生し、熱効率の低下、通水配管の閉塞、配管金属材質の
腐食等のスライム障害が起きる。また、スライム障害
は、紙パルププロセス水系、廃水処理水系等において
も、重大な問題を引き起こす。
2. Description of the Related Art In cooling water systems of various factory plants, slime composed of bacteria, filamentous fungi, algae, etc. is generated in the system, resulting in reduced thermal efficiency, clogging of water passage pipes, corrosion of pipe metal materials, etc. There is an obstacle. In addition, slime damage causes serious problems also in paper pulp process water systems, wastewater treatment water systems, and the like.

【0003】従来、冷却水系におけるスライム対策とし
ては、薬剤を用いる方法がとられており、薬剤として
は、付着したスライムを剥離ないし洗浄するスライム剥
離剤、洗浄剤、或いは、スライムの付着を防止するスラ
イムコントロール剤、殺菌剤がある。
Conventionally, as a measure against slime in a cooling water system, a method using a chemical agent has been taken. As the chemical agent, a slime removing agent for removing or cleaning the adhered slime, a cleaning agent, or preventing adhesion of slime is used. There are slime control agents and bactericides.

【0004】これらの薬剤のうち、スライムコントロー
ル剤、殺菌剤は、水中の微生物濃度を低く保つことによ
り、スライムの付着ポテンシャルを低減させることを目
的として使用されている。一般的に、スライムコントロ
ール剤は菌の酵素反応の阻害、細胞膜の変性作用によ
り、殺菌、抑制するといわれている。一方、スライム剥
離剤は、菌体外の粘着物質(一般には多糖類)の粘性を
なくすことにより、菌の集合体を分散し付着面より剥離
するものである。
Among these agents, slime control agents and bactericides are used for the purpose of reducing the adhesion potential of slime by keeping the concentration of microorganisms in water low. Generally, slime control agents are said to sterilize and suppress the enzymatic reaction of bacteria and the denaturing action of cell membranes. On the other hand, the slime stripping agent disperses aggregates of bacteria and removes them from the adhered surface by eliminating the viscosity of the adhesive substance (generally polysaccharides) outside the cells.

【0005】従来、スライム剥離剤、洗浄剤としては、
過酸化水素及びヒドラジンが用いられている。また、ス
ライムコントロール剤としてイソチアゾロン系化合物な
どが使用されている。
Conventionally, as a slime remover and a cleaning agent,
Hydrogen peroxide and hydrazine are used. Also, isothiazolone compounds are used as slime control agents.

【0006】[0006]

【発明が解決しようとする課題】従来、スライム剥離
剤、洗浄剤として用いられている過酸化水素及びヒドラ
ジンは、両者とも優れた効果を示すが、皮膚刺激性、廃
水処理等の面で問題があり、また、いずれも安全性の面
から代替品の出現が望まれている。
Hydrogen peroxide and hydrazine, which have hitherto been used as slime removers and detergents, both show excellent effects, but have problems in terms of skin irritation, wastewater treatment, etc. However, in all cases, the emergence of alternative products is desired from the viewpoint of safety.

【0007】一方、スライムコントロール剤や殺菌剤の
使用濃度は、増殖抑制限界以上で殺菌効果が実現するま
での範囲であり、スライムコントロール剤等のこのよう
な濃度レベルにおいては、スライム剥離効果は期待でき
ないし、また確認もされていない。因みに、従来、スラ
イムコントロール剤として使用されているイソチアゾロ
ン系化合物は、安全性は高いものの皮膚刺激性が強く、
実系では0.1〜0.5ppm程度の濃度範囲で使用さ
れている。しかして、このイソチアゾロン系化合物につ
いても、多糖類の粘性をなくすことによるスライム剥離
効果は全く予想されていなかった。
On the other hand, the use concentration of the slime control agent and the bactericide is in a range until the bactericidal effect is realized when the growth control limit is exceeded. I can't, and I haven't confirmed it. Incidentally, the isothiazolone compounds conventionally used as slime control agents are highly safe but have strong skin irritation.
In the actual system, it is used in a concentration range of about 0.1 to 0.5 ppm. However, even with this isothiazolone compound, the slime-stripping effect by eliminating the viscosity of the polysaccharide was not expected at all.

【0008】本発明は上記従来の実情に鑑みてなされた
ものであって、安全性の高い薬剤を用いて、冷却水系に
付着したスライムを、容易かつ効率的に、工業的に有利
に剥離する方法を提供することを目的とする。
The present invention has been made in view of the above-mentioned conventional circumstances, and the slime adhering to the cooling water system is easily and efficiently exfoliated industrially advantageously by using a highly safe chemical agent. The purpose is to provide a method.

【0009】[0009]

【課題を解決するための手段】本発明のスライム剥離方
法は、スライムが付着している水系にイソチアゾロン系
化合物を間欠的に添加することにより、該付着スライム
を剥離することを特徴とする。
The slime stripping method of the present invention is characterized in that the adhered slime is stripped by intermittently adding an isothiazolone compound to an aqueous system to which the slime is deposited.

【0010】即ち、本発明者らは、安全性の高いスライ
ム剥離剤を提供すべく、鋭意検討を重ねた結果、従来、
スライムコントロール剤として用いられてはいたが、ス
ライム剥離剤としての使用は全くなされておらず、ま
た、期待すらなされていなかったイソチアゾロン系化合
物が、多糖類の粘性をなくす作用を有し、スライム剥離
効果を発揮することを見出し、このイソチアゾロン系化
合物を用いる本発明のスライム剥離方法を完成させた。
That is, the inventors of the present invention have conducted extensive studies to provide a highly safe slime release agent, and as a result,
Although it was used as a slime control agent, it has not been used as a slime remover at all, and the isothiazolone compound, which was not even expected, has the action of eliminating the viscosity of polysaccharides, and it is used as a slime remover. It was found that the effect was exhibited, and the slime peeling method of the present invention using this isothiazolone compound was completed.

【0011】以下に本発明を詳細に説明する。The present invention will be described in detail below.

【0012】本発明においてスライム剥離剤として使用
されるイソチアゾロン系化合物としては、好ましくは、
下記一般式又はで示される化合物が挙げられる。
The isothiazolone compound used as the slime release agent in the present invention is preferably
The compounds represented by the following general formula or are included.

【0013】[0013]

【化1】 [Chemical 1]

【0014】具体的には、5−クロル−2−メチル−3
−イソチアゾロン、2−メチル−3−イソチアゾロン、
2−エチル−3−イソチアゾロン、4,5−ジクロル−
2−オクチル−3−イソチアゾロン、1,2−ベンゾイ
ソチアゾリン−3−オン、5−クロル−2−メチル−3
−イソチアゾロンマグネシウムナイトレート、2−メチ
ル−3−イソチアゾロンマグネシウムナイトレート、2
−エチル−3−イソチアゾロンカルシウムクロライド、
4,5−ジクロル−2−オクチル−3−イソチアゾロン
マグネシウムナイトレート等が挙げられる。
Specifically, 5-chloro-2-methyl-3
-Isothiazolone, 2-methyl-3-isothiazolone,
2-ethyl-3-isothiazolone, 4,5-dichloro-
2-octyl-3-isothiazolone, 1,2-benzisothiazolin-3-one, 5-chloro-2-methyl-3
-Isothiazolone magnesium nitrate, 2-methyl-3-isothiazolone magnesium nitrate, 2
-Ethyl-3-isothiazolone calcium chloride,
Examples include 4,5-dichloro-2-octyl-3-isothiazolone magnesium nitrate.

【0015】このようなイソチアゾロン系化合物は、こ
れをゲスト化合物として安定に包接し得るホスト化合物
との包接化合物として用いても良い。
Such an isothiazolone compound may be used as an inclusion compound with a host compound which can be stably included as a guest compound.

【0016】この場合、ホスト化合物としては、例え
ば、次の(1)〜(24)から選ばれる1種又は2種以
上の多分子系ホスト化合物を用いることができる。
In this case, as the host compound, for example, one kind or two or more kinds of multimolecular host compounds selected from the following (1) to (24) can be used.

【0017】(1) 1,1,6,6−テトラフェニル
−2,4−ヘキサジイン−1,6−ジオール (2) 1,6−ビス(2−クロロフェニル)−1,6
−ジフェニルヘキサ−2,4−ジイン−1,6−ジオー
ル (3) 1,1−ビス(2,4−ジメチルフェニル)−
2−プロピン−1−オール (4) 2,5−ビス(2,4−ジメチルフェニル)ハ
イドロキノン (5) 1,1,4,4−テトラフェニル−2−ブチン
−1,4−ジオール (6) 1,1,2,2−テトラフェニルエタン−1,
2−ジオール (7) 1,1−ビ−2−ナフトール (8) 9,10−ジフェニル−9,10−ジヒドロア
ントラセン−9,10−ジオール (9) 1,1,6,6−テトラキス(2,4−ジメチ
ルフェニル)−2,4−ヘキサジイン−1,6−ジオー
ル (10) 9,10−ビス(4−メチルフェニル)−
9,10−ジヒドロアントラセン−9,10−ジオール (11) 4,4’−シクロヘキシリデンビスフェノー
ル (12) N,N,N’,N’−テトラキス(シクロヘ
キシル)−(1,1’−ビフェニル)−2,2’−ジカ
ルボキシアミド (13) 1,4−ジアザビシクロ−(2,2,2)−
オクタン (14) 4,4’−スルホニルビスフェノール (15) 4,4’−ブチリデンビス(3−メチル−6
−tert−ブチルフェノール) (16) 2,2’−メチレンビス(4−メチル−6−
tert−ブチルフェノール) (17) 4,4’−チオビス(3−メチル−6−te
rt−ブチルフェノール) (18) 2,2’−メチレンビス(4−クロロフェノ
ール) (19) デオキシコール酸 (20) t−ブチルヒドロキノン (21) 2,5−ジ−tert−ブチルヒドロキノン (22) コール酸 (23) 顆粒状コーンスターチ(ポーラスY−20) (24) α,α,α’,α’−テトラフェニル−
1’,1’−ビフェニル−2,2’−ジメタノール これらのホスト化合物のうち、特に、水系に添加後一時
間以内に包接したイソチアゾロン系化合物の約90%以
上を放出するものが好ましい。
(1) 1,1,6,6-Tetraphenyl-2,4-hexadiyne-1,6-diol (2) 1,6-bis (2-chlorophenyl) -1,6
-Diphenylhexa-2,4-diyne-1,6-diol (3) 1,1-bis (2,4-dimethylphenyl)-
2-propyn-1-ol (4) 2,5-bis (2,4-dimethylphenyl) hydroquinone (5) 1,1,4,4-tetraphenyl-2-butyne-1,4-diol (6) 1,1,2,2-tetraphenylethane-1,
2-diol (7) 1,1-bi-2-naphthol (8) 9,10-diphenyl-9,10-dihydroanthracene-9,10-diol (9) 1,1,6,6-tetrakis (2 , 4-Dimethylphenyl) -2,4-hexadiyne-1,6-diol (10) 9,10-bis (4-methylphenyl)-
9,10-Dihydroanthracene-9,10-diol (11) 4,4'-Cyclohexylidenebisphenol (12) N, N, N ', N'-tetrakis (cyclohexyl)-(1,1'-biphenyl) -2,2'-dicarboxamide (13) 1,4-diazabicyclo- (2,2,2)-
Octane (14) 4,4'-sulfonylbisphenol (15) 4,4'-butylidene bis (3-methyl-6)
-Tert-butylphenol) (16) 2,2'-methylenebis (4-methyl-6-)
tert-butylphenol) (17) 4,4'-thiobis (3-methyl-6-te
rt-butylphenol) (18) 2,2′-methylenebis (4-chlorophenol) (19) deoxycholic acid (20) t-butylhydroquinone (21) 2,5-di-tert-butylhydroquinone (22) cholic acid (23) Granular corn starch (porous Y-20) (24) α, α, α ′, α′-tetraphenyl-
1 ', 1'-Biphenyl-2,2'-dimethanol Among these host compounds, those which release about 90% or more of the isothiazolone compound included in the aqueous system within 1 hour after addition are preferable.

【0018】なお、前記一般式で示されるイソチアゾ
ロン系化合物が上記ホスト化合物により包接化合物とさ
れた場合、包接時に錯体構造が解かれるため、包接され
た化合物は、前記一般式で示されるイソチアゾロン系
化合物となる。
When the isothiazolone compound represented by the general formula is converted into the inclusion compound by the host compound, the complex structure is unfolded during the inclusion, and thus the inclusion compound is represented by the general formula. It becomes an isothiazolone compound.

【0019】本発明において、イソチアゾロン系化合物
の好ましい添加濃度、添加形態は対象とする水系により
異なるが、例えば密閉循環冷却水系であれば、前記一般
式,で示されるイソチアゾロン系化合物そのものを
1ppm以上、特に3〜10ppm、とりわけ5〜6p
pm添加し、また、開放循環冷却水系であれば、イソチ
アゾロン系化合物の包接化合物を1ppm以上、特に3
〜10ppm、とりわけ5〜7ppm添加するのが好ま
しい。なお、イソチアゾロン系化合物を間欠添加する場
合の添加周期は、当該冷却水系のスライム付着状態に応
じて、1週間〜2ケ月に1回程度の範囲で適宜設定され
る。
In the present invention, the preferred concentration and mode of addition of the isothiazolone compound varies depending on the target water system. For example, in the case of a closed circulation cooling water system, the isothiazolone compound itself represented by the above general formula is 1 ppm or more, Especially 3-10ppm, especially 5-6p
pm addition, and if it is an open circulating cooling water system, the inclusion compound of the isothiazolone compound is 1 ppm or more, especially 3
It is preferable to add 10 to 10 ppm, especially 5 to 7 ppm. In addition, the addition cycle in the case of intermittently adding the isothiazolone compound is appropriately set within a range of about once a week to two months depending on the slime adhesion state of the cooling water system.

【0020】このような本発明の方法の処理対象となる
水系としては、冷却水系、紙パルププロセス水系、廃水
処理水系等の各種水系が挙げられる。
Examples of the water system to be treated by the method of the present invention include various water systems such as a cooling water system, a paper pulp process water system and a waste water treatment water system.

【0021】[0021]

【作用】イソチアゾロン系化合物は、スライム変性、脱
色作用を有し、多糖類の粘性をなくすことができる。こ
のため、イソチアゾロン系化合物の水系への間欠添加に
より、既に付着しているスライムを効果的に剥離するこ
とができる。
FUNCTION The isothiazolone compound has slime modification and decolorization effects and can eliminate the viscosity of the polysaccharide. Therefore, by intermittently adding the isothiazolone-based compound to the water system, the slime that has already adhered can be effectively removed.

【0022】特に、イソチアゾロン系化合物を適当なホ
スト化合物で包接してなる包接化合物の形態で用いるこ
とにより、その皮膚刺激性を低減し、取り扱い性を改善
することができる。
In particular, by using the isothiazolone compound in the form of an inclusion compound obtained by inclusion with an appropriate host compound, the skin irritation can be reduced and the handling property can be improved.

【0023】[0023]

【実施例】以下に実験例及び実施例を挙げて、本発明を
より具体的に説明する。
EXAMPLES The present invention will be described more specifically with reference to the following experimental examples and examples.

【0024】実験例1 厚木市水をバブリングして得られた脱塩素水1リットル
に、実際の工場の冷却水系から採取した汚れ成分(菌
体)を1重量%となるように添加し、更に5−クロロ−
2−メチル−3−イソチアゾロン(以下「CMI」と略
す。)と2,2’−メチレンビス(4−クロロフェノー
ル)とを3:7(重量比)の割合で含有する包接化合物
をCMIとして6mg/lとなるように添加した後、2
00rpmで5分間撹拌して分散させ、4日間室温下に
放置した。
Experimental Example 1 To 1 liter of dechlorinated water obtained by bubbling water from Atsugi City, soil components (bacteria) collected from an actual factory cooling water system were added so as to be 1% by weight. 5-chloro-
An inclusion compound containing 2-methyl-3-isothiazolone (hereinafter abbreviated as "CMI") and 2,2'-methylenebis (4-chlorophenol) in a ratio of 3: 7 (weight ratio) was 6 mg as CMI. / L, and then add 2
The mixture was stirred and dispersed at 00 rpm for 5 minutes, and left at room temperature for 4 days.

【0025】4日後に沈渣を取り出し、電子顕微鏡観察
を行なったところ、薬剤を何ら加えない場合には沈渣表
面に角ばった突起物や糸状物質が多数見られたが、薬剤
を加えた場合には、糸状物質が消失し、表面の突起物も
丸味を帯びた状態に変わっていた。この結果から、薬剤
はスライム剥離効果と表面改質効果が顕著であることが
わかる。
After 4 days, the precipitate was taken out and observed by an electron microscope. As a result, a large number of angular projections and filamentous substances were found on the surface of the sediment when no drug was added, but when a drug was added, The filamentous material disappeared, and the protrusions on the surface had also changed to a rounded state. From this result, it can be seen that the drug has a remarkable slime peeling effect and a surface modifying effect.

【0026】実施例1 100冷凍トン及び40冷凍トン規模の実工場の2ケ所
の開放循環冷却水系を対象として本発明の適用テストを
行なった。両水系に各々実験例1に用いた包接化合物を
6mg/lとなるように一括投入し、2週間通常の冷却
水系の運転を行なった。
Example 1 An application test of the present invention was carried out on two open circulating cooling water systems of an actual factory having a scale of 100 refrigeration tons and 40 refrigeration tons. The clathrate compound used in Experimental Example 1 was charged into both water systems at a rate of 6 mg / l, and the normal cooling water system was operated for 2 weeks.

【0027】2週間後に、100冷凍トンの冷却水系で
は冷却塔充填材について、一方、40冷凍トンの冷却水
系では水切板消音マットについて、目視観察により各々
処理効果の把握を行なった。
Two weeks later, the treatment effect was visually confirmed for the cooling tower filler in the cooling water system of 100 refrigeration tons, and for the draining board muffling mat in the cooling water system of 40 refrigeration tons.

【0028】その結果、冷却塔充填材については、当初
充填材全面に濃緑〜茶褐色のスライムが約3mmの厚さ
で付着していたが、2週間後には殆どのスライムは剥離
するか、又は、付着していても厚みが感じられない程度
まで剥離していることがわかった。なお、付着スライム
は緑色に変色した。
As a result, regarding the cooling tower filler, dark green to brownish slime was initially adhered to the entire surface of the filler with a thickness of about 3 mm, but after two weeks most of the slime was peeled off, or It was found that even if they were attached, they were peeled off to the extent that the thickness was not felt. The adhered slime turned green.

【0029】一方、水切板消音マットについても処理前
には海苔状のスライムがマット一面に付着していたが、
処理後には、スライムは殆ど消失していることがわかっ
た。
On the other hand, in the draining board sound deadening mat, nori-like slime adhered to the entire surface of the mat before the treatment.
It was found that the slime had almost disappeared after the treatment.

【0030】なお、いずれの場合にも処理中、CMI特
有の皮膚刺激性は全く感じられなかった。
In any case, no skin irritation peculiar to CMI was felt during the treatment.

【0031】[0031]

【発明の効果】以上詳述した通り、本発明のスライム剥
離方法によれば、イソチアゾロン系化合物を用いて、水
系に既に付着しているスライムを、容易かつ効率的に、
工業的に有利に剥離することが可能とされる。
As described in detail above, according to the slime stripping method of the present invention, the isothiazolone compound is used to easily and efficiently remove slime already attached to the water system.
It is possible to peel off industrially advantageously.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 スライムが付着している水系にイソチア
ゾロン系化合物を間欠的に添加することにより、該付着
スライムを剥離することを特徴とするスライム剥離方
法。
1. A slime stripping method, wherein the deposited slime is stripped by intermittently adding an isothiazolone compound to an aqueous system to which slime is deposited.
JP3320503A 1991-12-04 1991-12-04 Slime peeling method Expired - Fee Related JP2565043B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3320503A JP2565043B2 (en) 1991-12-04 1991-12-04 Slime peeling method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3320503A JP2565043B2 (en) 1991-12-04 1991-12-04 Slime peeling method

Publications (2)

Publication Number Publication Date
JPH05155719A true JPH05155719A (en) 1993-06-22
JP2565043B2 JP2565043B2 (en) 1996-12-18

Family

ID=18122179

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3320503A Expired - Fee Related JP2565043B2 (en) 1991-12-04 1991-12-04 Slime peeling method

Country Status (1)

Country Link
JP (1) JP2565043B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009215271A (en) * 2008-03-13 2009-09-24 Aquas Corp Biofilm releasant, and method for releasing biofilm
JP2012214388A (en) * 2011-03-31 2012-11-08 Aquas Corp Biofilm peeling agent, and method for peeling the biofilm
JP2014181247A (en) * 2013-03-18 2014-09-29 Fujitsu Ltd Biofilm remover, biofilm removal method and information processing apparatus
WO2015046016A1 (en) * 2013-09-24 2015-04-02 栗田工業株式会社 Antimicrobial and algicidal method for cooling water system and antimicrobial and algicidal agent

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54140726A (en) * 1978-04-24 1979-11-01 Somar Mfg Slime controlling agent in paper pulp industry
JPS55129104A (en) * 1979-03-27 1980-10-06 Nitto Electric Ind Co Ltd Sterilizing treating method for membrane separation unit
JPS5980606A (en) * 1982-10-29 1984-05-10 Kurita Water Ind Ltd Agent for preventing deposition of sludge
JPS6210003A (en) * 1985-07-05 1987-01-19 Katayama Chem Works Co Ltd Industrial fungicidal and algicidal agent
JPH01190601A (en) * 1988-01-25 1989-07-31 Kurita Water Ind Ltd Production of clathrate compound
JPH03178906A (en) * 1989-12-06 1991-08-02 Kurita Water Ind Ltd Production of clathrate compound

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54140726A (en) * 1978-04-24 1979-11-01 Somar Mfg Slime controlling agent in paper pulp industry
JPS55129104A (en) * 1979-03-27 1980-10-06 Nitto Electric Ind Co Ltd Sterilizing treating method for membrane separation unit
JPS5980606A (en) * 1982-10-29 1984-05-10 Kurita Water Ind Ltd Agent for preventing deposition of sludge
JPS6210003A (en) * 1985-07-05 1987-01-19 Katayama Chem Works Co Ltd Industrial fungicidal and algicidal agent
JPH01190601A (en) * 1988-01-25 1989-07-31 Kurita Water Ind Ltd Production of clathrate compound
JPH03178906A (en) * 1989-12-06 1991-08-02 Kurita Water Ind Ltd Production of clathrate compound

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009215271A (en) * 2008-03-13 2009-09-24 Aquas Corp Biofilm releasant, and method for releasing biofilm
JP2012214388A (en) * 2011-03-31 2012-11-08 Aquas Corp Biofilm peeling agent, and method for peeling the biofilm
JP2014181247A (en) * 2013-03-18 2014-09-29 Fujitsu Ltd Biofilm remover, biofilm removal method and information processing apparatus
WO2015046016A1 (en) * 2013-09-24 2015-04-02 栗田工業株式会社 Antimicrobial and algicidal method for cooling water system and antimicrobial and algicidal agent

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