JPS6320090A - Water cleaning agent and its production - Google Patents

Water cleaning agent and its production

Info

Publication number
JPS6320090A
JPS6320090A JP16444786A JP16444786A JPS6320090A JP S6320090 A JPS6320090 A JP S6320090A JP 16444786 A JP16444786 A JP 16444786A JP 16444786 A JP16444786 A JP 16444786A JP S6320090 A JPS6320090 A JP S6320090A
Authority
JP
Japan
Prior art keywords
water
carrier
silver salt
silver
cleaning agent
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
JP16444786A
Other languages
Japanese (ja)
Inventor
Michiharu Arita
有田 道治
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.)
ASAHI KANKO KK
Original Assignee
ASAHI KANKO 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 ASAHI KANKO KK filed Critical ASAHI KANKO KK
Priority to JP16444786A priority Critical patent/JPS6320090A/en
Publication of JPS6320090A publication Critical patent/JPS6320090A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To maintain excellent sterilization performance for a long period of time by using a water cleaning agent prepd. by depositing a hardly soluble silver salt on a silica-alumina porous inorg. carrier in water. CONSTITUTION:An aq. silver nitrate soln. is added to the silica-alumina porous inorg. carrier (e.g., silica gel) and thereafter, a halogen compd. (e.g., salt water) is acted thereto to deposit the hardly soluble silver salt (e.g., AgCl) on the carrier at the time of depositing the silver salt onto said carrier. The water cleaning agent produced in such a manner has the excellent sterilization performance and is capable of maintaining the capacity for a long period of time. Since there are no exfoliation of the silver salt, the dissolution of the carrier, etc., the safe use of the treated water and the protection of the device are possible. Since the stable silica gel carrier is usable, the inexpensive provision of the water cleaning agent is feasible.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明はビル冷却塔水やプール@環水等の水中微生物の
殺菌や殺藻を目的とした浄水剤及びその製造方法に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a water purifying agent for the purpose of sterilizing microorganisms and killing algae in water such as building cooling tower water and swimming pool water, and a method for producing the same.

〈従来の技術〉 在郷軍人病(レジオネジ症)の原因として知られている
貯水中のバクテリアの繁殖に対して、これを抑制するた
めに金属イオンの存在が有効であることは公知である。
<Prior Art> It is known that the presence of metal ions is effective in suppressing the proliferation of bacteria in stored water, which is known to be the cause of Legionnaires' Disease.

なかでも銀イオンの存在は最も有効で、そこで、これを
用いてクーリングタワー等の殺菌や殺藻が行われている
Among these, the presence of silver ions is the most effective, and is therefore used to sterilize cooling towers and kill algae.

貯水中に銀イオンを作用させる際に必要なことは、銀イ
オンの水中濃度が適度に抑えられ、かつ。
When silver ions are used in stored water, what is required is that the concentration of silver ions in the water be moderately suppressed, and.

長期に亘って銀イオンの供給が可能なことである。It is possible to supply silver ions over a long period of time.

そこで、銀化合物を直接貯水中へ投入するのではなく、
ガラス中に銀化合物を含ませて粒子状にしたものや、活
性炭に銀を担持させたもの(特公昭52−38666号
)を水中に入れて、徐々に銀イオンを溶出させる構造の
ものが提案され、また市販されている。
Therefore, instead of putting silver compounds directly into the storage water,
Proposed structures include glass containing silver compounds in the form of particles, or activated carbon carrying silver (Special Publication No. 38666/1989), which is placed in water to gradually elute silver ions. and is also commercially available.

〈発明が解決しようとする問題点〉 しかし、アモルファスガラス中に恨化合物を含ませて粒
子状にしたものは、ホウ珪酸系ガラス自身が溶解すると
いった性質を利用しているので、溶解したガラスが水中
に存在することと、循環系のいずれかの場所にそのガラ
スが析出する難点が指摘されている。また、アモルファ
スガラスは溶解が進むにつれて表面が変化して次第に銀
の溶出量が減る難点を有している。活性炭に銀を担持さ
せたものは、活性炭と銀化合物との親和性が小さいので
、活性炭から銀が物理的に剥雅し易く、長期の使用に耐
え得ない(1ケ月以上その性能を保ち続けることは慧し
い)!!、点を有している。
<Problems to be solved by the invention> However, the amorphous glass that is made into particles by impregnating it with a compound takes advantage of the property of the borosilicate glass itself to melt, so the melted glass is It has been pointed out that glass exists in water and that the glass is deposited somewhere in the circulation system. In addition, amorphous glass has the disadvantage that as melting progresses, the surface changes and the amount of silver eluted gradually decreases. Activated carbon with silver supported has a low affinity between the activated carbon and the silver compound, so the silver easily peels off from the activated carbon and cannot withstand long-term use (it maintains its performance for more than a month). That's a shame)! ! , has a point.

く問題点を解決するための手段〉 そこで本発明者らは、シリカ・アルミナ系多孔質無機担
体の吸着能に着目し、これに、芝溶性銀塩を担持させて
なる浄水剤を開発したのである。
Means for Solving the Problems> Therefore, the present inventors focused on the adsorption ability of a silica-alumina porous inorganic carrier and developed a water purifying agent in which a grass-soluble silver salt is supported on the carrier. be.

その浄水剤は、シリカ・アルミナ系多孔質無機担体に銀
塩を担持させるに際して、同担体に硝酸銀水溶液を添加
した後、ハロゲン化合物等を作用させて難溶性の銀塩と
して担持させることにより製造することができる。
The water purifying agent is produced by supporting a silver salt on a silica/alumina porous inorganic carrier, adding an aqueous silver nitrate solution to the carrier, and then applying a halogen compound or the like to support the silver salt as a sparingly soluble silver salt. be able to.

ここにいうl溶性銀塩とは、A、CQ、A g B r
、A[Xl、Ag2O,AgC2H502、AgBrO
3、Ag2CO3,Ag2Cr0,1.AgOH等の溶
解度が低い銀塩である。
The soluble silver salts mentioned here are A, CQ, A g B r
, A[Xl, Ag2O, AgC2H502, AgBrO
3, Ag2CO3, Ag2Cr0,1. It is a silver salt with low solubility such as AgOH.

また、シリカ・アルミナ系多孔質無機担体とは、汎用さ
れているシリカゲルやゼオライト、パーライト等を含み
、多孔質構造のものである。
The silica-alumina porous inorganic carrier includes widely used silica gel, zeolite, perlite, etc., and has a porous structure.

く作用〉 シリカ・アルミナ系多孔質無機担体に銀塩を担持させた
浄水剤は、銀と化合するハロゲン等の種類によって溶解
度が異なり、水中の銀濃度を低濃度の必要濃度に保つ作
用がある。この適度かつ長期に亘って水中り;存在する
銀が殺菌作用をする。
Water purification agents that have silver salt supported on a silica/alumina porous inorganic carrier have different solubility depending on the type of halogen that combines with silver, and have the effect of keeping the silver concentration in water at a low required concentration. . During this moderate and long-term immersion in water, the silver present has a bactericidal effect.

〈実施例〉 以下実施例によって本発明の詳細な説明する。<Example> The present invention will be explained in detail below with reference to Examples.

約500ccのシリカゲルに5%硝酸銀水溶液約100
ccをシリカゲルに全量が吸収される程度に加減しなが
ら加えた。 この場合、硝酸銀は5gを目安とするが、
 この場合、5〜10gの間にシリカゲルの吸着飽和点
がある。これを約1時間放匝して硝酸銀を吸着させた。
Approximately 100 ml of 5% silver nitrate aqueous solution in approximately 500 cc of silica gel
cc was added in a controlled manner until the entire amount was absorbed into the silica gel. In this case, the standard amount of silver nitrate is 5g,
In this case, the adsorption saturation point of silica gel is between 5 and 10 g. This was left to stand for about 1 hour to adsorb silver nitrate.

次に20%食塩水500ccを上記シリカゲルに注いで
、反応させた。この化学反応によって。
Next, 500 cc of 20% saline solution was poured into the silica gel and reacted. by this chemical reaction.

AgN0 a−+ AgCQ となり、約1時間で総ての反応を終えてシリカゲルに塩
化銀が吸着された。これを約80℃のオーブン中で1時
間加熱乾燥して浄水剤を得た。同様にして第1表に示す
ような水に対するM溶性の各種銀化合物を担持させた。
AgN0 a-+ AgCQ was obtained, and the entire reaction was completed in about 1 hour, and silver chloride was adsorbed on the silica gel. This was heated and dried in an oven at about 80° C. for 1 hour to obtain a water purifier. In the same manner, various water-soluble silver compounds as shown in Table 1 were supported.

第1表は担持された各銀化合物の溶解度及びそれぞれの
浄水剤の100gを、5日間、流水中に浸漬した時、流
水中に含まれる各化合物の濃度を原子吸光分析法で測定
した結果を示している。
Table 1 shows the solubility of each supported silver compound and the results of measuring the concentration of each compound contained in running water using atomic absorption spectrometry when 100 g of each water purifying agent was immersed in running water for 5 days. It shows.

第1表 以上の結果から明らかなように、本発明の浄水剤は30
〜50ppbの適度な銀イオンを長期に亘って水中へ放
出することができろ。
As is clear from the results in Table 1 and above, the water purifying agent of the present invention
Moderate silver ions of ~50 ppb can be released into water over a long period of time.

殺菌効果試験 次にAgイオンを含む従来のアモルファスガラス及び本
発明に係るAgイオンを含むシリカゲルをポリバケツに
浸漬して、溶は出すAgイオンの殺菌効果を大腸菌の存
在する水によって試験した。
Bactericidal effect test Next, the conventional amorphous glass containing Ag ions and the silica gel containing Ag ions according to the present invention were immersed in a poly bucket, and the bactericidal effect of the dissolved Ag ions was tested using water containing Escherichia coli.

使用菌株はEschericha Co11であって、
使用培地は普通寒天培地(日本製薬味製)を用いた。
The strain used was Eschericha Co11,
The medium used was an ordinary agar medium (manufactured by Nihon Pharmaceutical Aji).

用意した2個のボリパケツ中にIORの水をそれぞれ入
れ、前記Agイオンを含むアモルファスガラス及びシリ
カゲルを6g宛とり、 それぞれを前記バケツ中に入れ
て浸漬した。バケツ中より毎日1回lθ%すなわちIQ
の水を捨て1代りに新しい水をIQ加えて、 この操作
を 1週間繰返えしてAgイオン溶出試験水を得た。
IOR water was poured into two prepared buckets, and 6 g of the Ag ion-containing amorphous glass and silica gel were each placed in the buckets and immersed. lθ% or IQ once a day from a bucket
The water was discarded, new water was added in its place, and this operation was repeated for one week to obtain Ag ion elution test water.

次に、生理食塩水3ccを使って前記大腸菌の菌液を作
り、3等分して同濃度の標準菌液を試験管に3本用意し
た。この3本の試験管中へ前記2種のAgイオン溶出試
験水を3cc宛採取してそれぞれ加え、残りの1本の試
験管中にはブランクとして無菌の蒸溜水3ccを加えた
Next, a bacterial solution of E. coli was prepared using 3 cc of physiological saline, divided into three equal parts, and three standard bacterial solutions of the same concentration were prepared in test tubes. 3 cc of the two types of Ag ion elution test waters were collected and added to each of the three test tubes, and 3 cc of sterile distilled water was added to the remaining test tube as a blank.

これらの試験管中から5時間後、24時間後にそれぞれ
Ice宛採取し、寒天培地で混釈培養して24時間後に
菌数を測定した。その結果を第2表に示した。
After 5 hours and 24 hours, the cells were collected from these test tubes on ice, poured into an agar medium, and cultured, and the number of bacteria was counted 24 hours later. The results are shown in Table 2.

第2表 第2表で明らかなように1本発明の浄水剤の殺+M効果
は従来品に比べて非常に良好である。
As is clear from Table 2, the water purifying agent of the present invention has a much better killing +M effect than conventional products.

本発明においてシリカゲルと水に難溶性の銀塩が対象と
なった最も大きな要因は、長期間、少くとも数ケ月の間
持続させて銀イオンを水中へ放出する能力を持たせるた
めであるが、その他に、木中銀イオン濃度は飲tト水に
ついては50ppb以下に米国公衆衛生局で定められて
おり、緊急の場合には海水を軟化させるために塩化銀の
飽和水を飲用として用いるとされているくらいであるか
ら、毒性についてはあまり問題とされないものの、飲料
水の浄化に本発明品を用いることも可能とするためであ
る。
The main reason why silica gel and poorly water-soluble silver salts are used in the present invention is to have the ability to release silver ions into water for a long period of time, at least several months. In addition, the U.S. Public Health Service has set the Kichu silver ion concentration at 50 ppb or less for drinking water, and in case of an emergency, silver chloride-saturated water should be used for drinking to soften seawater. This is because the product of the present invention can also be used to purify drinking water, although toxicity is not much of a problem.

〈発明の効果〉 以上詳述したように本発明の浄水剤は殺菌性能に優れ、
しかも長期に亘ってその能力を維持することができる。
<Effects of the Invention> As detailed above, the water purifying agent of the present invention has excellent bactericidal performance,
Furthermore, this ability can be maintained over a long period of time.

また、銀塩の剥離とか担体の溶解等がないので、処理水
の安全な使用と装置の保護ができる。安価なシリカゲル
担体の使用が可能であるから、製品の安価な提供が可能
となった。
Furthermore, since there is no peeling of the silver salt or dissolution of the carrier, the treated water can be used safely and the equipment can be protected. Since it is possible to use an inexpensive silica gel carrier, it has become possible to provide products at low cost.

また、用途もクーリングタワーやプールの浄水剤以外に
、浴場、工業用水の各種殺菌、殺藻、防錆剤、工作機械
の切削油の殺菌、防錆剤等にも広く応用できるものであ
る。
In addition to water purification agents for cooling towers and swimming pools, it can also be used in various sterilizations for baths and industrial water, as an algaecide, as a rust preventive agent, as a sterilizer for machine tool cutting oil, and as a rust preventive agent.

以上that's all

Claims (1)

【特許請求の範囲】 1 シリカ・アルミナ系多孔質無機担体に、難溶性銀塩
を担持させてなることを特徴とする浄水剤。 2 シリカ・アルミナ系多孔質無機担体に銀塩を担持さ
せるに際して、同担体に硝酸銀水溶液を添加した後、ハ
ロゲン化合物等を作用させて難溶性の銀塩を担持させる
ことを特徴とする浄水剤の製造方法。
[Scope of Claims] 1. A water purifier comprising a silica-alumina porous inorganic carrier supporting a sparingly soluble silver salt. 2. A water purifying agent characterized in that when a silver salt is supported on a silica/alumina-based porous inorganic carrier, an aqueous silver nitrate solution is added to the carrier, and then a halogen compound or the like is applied to support the poorly soluble silver salt. Production method.
JP16444786A 1986-07-12 1986-07-12 Water cleaning agent and its production Pending JPS6320090A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16444786A JPS6320090A (en) 1986-07-12 1986-07-12 Water cleaning agent and its production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16444786A JPS6320090A (en) 1986-07-12 1986-07-12 Water cleaning agent and its production

Publications (1)

Publication Number Publication Date
JPS6320090A true JPS6320090A (en) 1988-01-27

Family

ID=15793339

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16444786A Pending JPS6320090A (en) 1986-07-12 1986-07-12 Water cleaning agent and its production

Country Status (1)

Country Link
JP (1) JPS6320090A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0212496U (en) * 1988-07-06 1990-01-25
JPH02251292A (en) * 1989-03-24 1990-10-09 Shinagawa Nenryo Kk Sterilizing material for cooling tower

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0212496U (en) * 1988-07-06 1990-01-25
JPH02251292A (en) * 1989-03-24 1990-10-09 Shinagawa Nenryo Kk Sterilizing material for cooling tower
JPH0512038B2 (en) * 1989-03-24 1993-02-17 Shinagawa Nenryo Kk

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