JPH0373359B2 - - Google Patents

Info

Publication number
JPH0373359B2
JPH0373359B2 JP59006796A JP679684A JPH0373359B2 JP H0373359 B2 JPH0373359 B2 JP H0373359B2 JP 59006796 A JP59006796 A JP 59006796A JP 679684 A JP679684 A JP 679684A JP H0373359 B2 JPH0373359 B2 JP H0373359B2
Authority
JP
Japan
Prior art keywords
acid
organic acids
piping
calcium carbonate
inorganic
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.)
Expired - Lifetime
Application number
JP59006796A
Other languages
Japanese (ja)
Other versions
JPS60150899A (en
Inventor
Ichiro Ito
Kyosuke Mizuno
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 JP679684A priority Critical patent/JPS60150899A/en
Publication of JPS60150899A publication Critical patent/JPS60150899A/en
Publication of JPH0373359B2 publication Critical patent/JPH0373359B2/ja
Granted legal-status Critical Current

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  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は付着物溶解剤に関するものである。 空調設備や工場のプロセス配管などには、水や
空気から持ち込まれた硬度成分や管の腐食などの
ために管内に炭酸カルシウムなどを主成分とする
無機系スケールや酸化鉄を主成分とする腐食生成
物が析出、堆積する。このような付着物は運転効
率を著しく劣化させるのでできるだけ除去しなけ
ればならない。 従来、このような配管内の付着物を除去するた
めに塩酸、硫酸、硝酸などの無機酸が多用されて
きた。 しかし、これらの無機酸はPHが極めて低いため
取扱いが危険であるばかりではなく、配管などの
材質に対して腐食性が著しいという問題点があつ
た。 一方、修酸やクエン酸などの有機酸も一般的に
洗浄剤として知られている。このうち、修酸の場
合には酸化鉄に対する溶解力が強いため酸洗浄剤
として良く用いられているが、特にカルシウム系
のスケールを対象とする場合には、溶解効率がそ
れほど十分ではなく、実用上問題があつた。 また、それ以外の有機酸についても、単独使用
では両無機系スケールに対する溶解効果が充分で
なく、実用的とは言えなかつた。 この発明はこれら従来技術の持つ問題点を解決
するために鋭意研究された結果完成されたもので
あり、極めて効率的な付着物溶解剤を提供するこ
とを目的とするものである。 すなわち、この発明はHOOC−(CH2)n−
COOH(nは0〜4の整数を表わす)で表わされ
る有機酸を2種以上含む炭酸カルシウム又は酸化
鉄を含む無機系付着物溶解剤である。 上記の構造式で表われる二塩基酸の具体例とし
ては、修酸、マロン酸、コハク酸、グルタル酸及
びアジピン酸が挙げられる。 この発明では、これら二塩基酸を複数含むこと
を必須要件とするものであるが、2種以上含んで
おればよく、3種でも5種でもよい。配合割合に
ついても特に限定されず、後述の実施例でも明ら
かなように僅かに異種成分を添加しただけでも相
乗効果により溶解効率が大巾に改善される。 実施に際しては、先ず用いる有機酸を適当割合
混ぜ合わし、水溶液とする。その濃度は0.01%以
上、好ましくは0.1%以上とするほうが溶解効率
上望ましい。 こうして得られた溶解剤は、次に対象とする系
に供給し、ポンプ等で循環する。液温は通常室温
〜30℃程度、循環時間は0.5〜数時間程度とする。 終了後、溶解液は全量排出し、別途必要に応じ
て適宜処理処分する。 なお、この発明の溶解剤は、必要に応じて他の
公知の洗浄剤、たとえばクエン酸、リンゴ酸など
の有機酸や塩酸などの無機酸および公知の酸洗用
腐食防止剤をさらに配合することができる。 この発明の対象とする系は、ビル、マンシヨ
ン、工場などの空調設備、工場のプロセスの配
管、冷却水系などが挙げられる。特定の二塩基酸
を2種以上配合することにより、従来知られてい
なかつたような相乗効果が得られ、その結果、効
率的に配管系等に付着した付着物を溶解除去する
ことができる。 実施例 1 ビルは給水の配管から採集した鉄錆10gをビー
カーに取り、第1表に記載した配合割合の有機酸
の水溶液(5W/V%)1を加え、室温下、撹
拌しながら3時間反応させた。 3時間後、ビーカーを静置し、上澄水中の鉄イ
オン濃度を測定した。結果を第1表に示す。 第1表から、修酸単独使用の場合より、異種の
有機酸を配合した方がはるかに溶解量が多いこと
がわかる。
This invention relates to a deposit dissolving agent. In air conditioning equipment and factory process piping, corrosion occurs due to hardness components brought in from water and air and corrosion of the pipes, including inorganic scale mainly composed of calcium carbonate and iron oxide. The product precipitates and accumulates. Such deposits must be removed as much as possible since they significantly degrade operating efficiency. Conventionally, inorganic acids such as hydrochloric acid, sulfuric acid, and nitric acid have been frequently used to remove such deposits inside piping. However, these inorganic acids have an extremely low pH and are not only dangerous to handle, but also have the problem of being extremely corrosive to materials such as piping. On the other hand, organic acids such as oxalic acid and citric acid are also generally known as cleaning agents. Among these, oxalic acid has a strong dissolving power for iron oxide, so it is often used as an acid cleaning agent.However, especially when targeting calcium-based scale, the dissolving efficiency is not very sufficient and it is not practical. There was a problem above. Furthermore, when other organic acids are used alone, they do not have a sufficient dissolving effect on both inorganic scales, and cannot be said to be practical. This invention was completed as a result of intensive research to solve the problems of the prior art, and its purpose is to provide an extremely efficient deposit dissolving agent. That is, this invention provides HOOC-( CH2 )n-
It is an inorganic deposit dissolving agent containing calcium carbonate or iron oxide containing two or more organic acids represented by COOH (n represents an integer from 0 to 4). Specific examples of the dibasic acid represented by the above structural formula include oxalic acid, malonic acid, succinic acid, glutaric acid, and adipic acid. In this invention, it is essential to contain a plurality of these dibasic acids, but it is sufficient to contain two or more types, and it may be three or five types. The blending ratio is not particularly limited either, and as is clear from the Examples described later, even if a small amount of different components are added, the dissolution efficiency can be greatly improved due to the synergistic effect. In implementation, first, the organic acids to be used are mixed in appropriate proportions to form an aqueous solution. It is desirable for the concentration to be 0.01% or more, preferably 0.1% or more in terms of dissolution efficiency. The solubilizer thus obtained is then supplied to the target system and circulated using a pump or the like. The liquid temperature is usually about room temperature to 30°C, and the circulation time is about 0.5 to several hours. After completion of the dissolution, the entire amount of the solution is discharged and separately treated and disposed of as necessary. The solubilizing agent of the present invention may further contain other known cleaning agents, such as organic acids such as citric acid and malic acid, inorganic acids such as hydrochloric acid, and known corrosion inhibitors for pickling, if necessary. I can do it. Systems targeted by this invention include air conditioning equipment for buildings, apartments, factories, etc., factory process piping, cooling water systems, and the like. By blending two or more specific dibasic acids, a previously unknown synergistic effect can be obtained, and as a result, deposits attached to piping systems etc. can be efficiently dissolved and removed. Example 1 10g of iron rust collected from the building's water supply piping was placed in a beaker, an aqueous solution of organic acid (5W/V%) 1 was added at the mixing ratio listed in Table 1, and the mixture was stirred at room temperature for 3 hours. Made it react. After 3 hours, the beaker was left still and the iron ion concentration in the supernatant water was measured. The results are shown in Table 1. From Table 1, it can be seen that the amount dissolved is much greater when different types of organic acids are blended than when oxalic acid is used alone.

【表】 実施例 2 石油精製工場の冷却塔充填物に付着した炭酸カ
ルシウムを主成分とするスケール10gをビーカー
に取り、実施例1と同様の方法で、第2表に示す
溶解剤を用いて実施した。結果を第2表に示す。 第2表から、この発明の溶解剤が比較例と比べ
てはるかに効果が良いことがわかる。
[Table] Example 2 10g of scale mainly composed of calcium carbonate attached to the cooling tower packing of an oil refinery was taken into a beaker and treated in the same manner as in Example 1 using the dissolving agent shown in Table 2. carried out. The results are shown in Table 2. From Table 2, it can be seen that the dissolving agent of the present invention is much more effective than the comparative example.

【表】 実施例 3 スケールの析出した工場の空調用冷却水系(保
有水量100)を対象として洗浄試験を、行なつ
た。スケールは分析したところ炭酸カルシウム60
%、酸化鉄10%から構成されていた。 用いた溶解剤はアジピン酸10%+グルタル酸65
%+コハク酸25%であつた。 この溶解剤10Kgをポンプ循環により冷却水系に
供給した。25℃下1時間溶解反応を行なわせた。 1時間後溶解液を排出し、液を分析したとこ
ろ、カルシウムイオン3.000mg/、及び鉄イオ
ン250mg/が検出された。 水洗後、冷却装置の運転を再開したところ、洗
浄前と比べて電気使用量が10%少なくてすんだ。 なお、洗浄中、冷却水系内に浸漬したテストピ
ース(軟鋼、純銅、アルミニウム黄銅、SUS)
の腐食速度はいずれも1mg/cm2/hr以下であり、
腐食問題は全くないことがわかつた。 比較のため同工場の別の空調用冷却水系をグル
タル酸10Kgのみを用いて上記と同様の操作で洗浄
したところ、液中のカルシウム硬度は100mg/
−CaCO3にすぎなかつた。
[Table] Example 3 A cleaning test was conducted on an air conditioning cooling water system (water capacity: 100) in a factory where scale had precipitated. The scale was analyzed and found to be calcium carbonate 60.
%, and 10% iron oxide. The solubilizer used was 10% adipic acid + 65% glutaric acid.
% + 25% succinic acid. 10 kg of this solubilizer was supplied to the cooling water system by pump circulation. The dissolution reaction was carried out at 25°C for 1 hour. After 1 hour, the dissolved solution was drained and analyzed, and 3.000 mg of calcium ions and 250 mg of iron ions were detected. When the cooling system was restarted after washing, electricity consumption was 10% lower than before washing. In addition, test pieces (mild steel, pure copper, aluminum brass, SUS) immersed in the cooling water system during cleaning.
The corrosion rate of each is less than 1 mg/cm 2 /hr,
It was found that there were no corrosion problems at all. For comparison, another air conditioning cooling water system at the same factory was cleaned in the same manner as above using only 10 kg of glutaric acid, and the calcium hardness in the liquid was 100 mg/kg.
-It was only CaCO 3 .

Claims (1)

【特許請求の範囲】[Claims] 1 HOOC−(CH2)n−COOH(nは0〜4の
整数を表わす)で表わされる有機酸を2種以上含
むことを特徴とする、炭酸カルシウム又は酸化鉄
を含む無機系付着物溶解剤。
1. An inorganic deposit dissolving agent containing calcium carbonate or iron oxide, characterized by containing two or more organic acids represented by HOOC-( CH2 )n-COOH (n represents an integer from 0 to 4) .
JP679684A 1984-01-18 1984-01-18 Dissolving agent of adhered material Granted JPS60150899A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP679684A JPS60150899A (en) 1984-01-18 1984-01-18 Dissolving agent of adhered material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP679684A JPS60150899A (en) 1984-01-18 1984-01-18 Dissolving agent of adhered material

Publications (2)

Publication Number Publication Date
JPS60150899A JPS60150899A (en) 1985-08-08
JPH0373359B2 true JPH0373359B2 (en) 1991-11-21

Family

ID=11648135

Family Applications (1)

Application Number Title Priority Date Filing Date
JP679684A Granted JPS60150899A (en) 1984-01-18 1984-01-18 Dissolving agent of adhered material

Country Status (1)

Country Link
JP (1) JPS60150899A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3542970A1 (en) * 1985-12-05 1987-06-11 Benckiser Gmbh Joh A LIQUID SANITARY CLEANING AND DECALCIFYING AGENTS AND METHOD FOR THE PRODUCTION THEREOF
US5895763A (en) * 1997-04-16 1999-04-20 H.E.R.C. Products Incorporated Controlled carbonate removal from water conduit systems
US7639827B2 (en) * 2003-10-01 2009-12-29 Phonak Ag Hearing system which is responsive to acoustical feedback

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS565195A (en) * 1979-06-27 1981-01-20 Nissan Chem Ind Ltd Removal of scale

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS565195A (en) * 1979-06-27 1981-01-20 Nissan Chem Ind Ltd Removal of scale

Also Published As

Publication number Publication date
JPS60150899A (en) 1985-08-08

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