JPS6086286A - Water treating chemical agent - Google Patents
Water treating chemical agentInfo
- Publication number
- JPS6086286A JPS6086286A JP9629983A JP9629983A JPS6086286A JP S6086286 A JPS6086286 A JP S6086286A JP 9629983 A JP9629983 A JP 9629983A JP 9629983 A JP9629983 A JP 9629983A JP S6086286 A JPS6086286 A JP S6086286A
- Authority
- JP
- Japan
- Prior art keywords
- water
- salt
- chemical agent
- acid
- corrosion
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は水と接触している金属の防護のための水処理薬
剤に関する。更に詳しくは、循環冷却水系統、温水系統
その他の通水系統の水と接触している金属壁面を腐食、
スケールその他の懸濁物の付着から保護するための水処
理薬剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to water treatment agents for the protection of metals in contact with water. More specifically, metal walls in contact with water in circulating cooling water systems, hot water systems, and other water circulation systems are corroded.
The present invention relates to water treatment agents for protecting against adhesion of scale and other suspended matter.
いかなる通水系統もその通水管素材が非耐食性であれば
、腐食に対する防護を怠るのけ危険である。空調システ
ムの如き循環冷却水系統でけ、冷却水を循環して再利用
するので、またブロー水量を抑制するのが一般管理方法
でもあるので、冷却水の濃縮化を来たし、塩類濃度が増
加することとなり、このため壁面へのスケール、懸濁物
の沈着、これ等に伴う金属の腐食の増大が惹き起こされ
スケール障害、腐食障害を発生し易い。装置熱交換器な
どの熱伝導面に付着したスケール等は、熱交換率の低下
の原因と亀なり高圧力ットを招くおそれもある。配管中
のさびこぶは、閉塞事故、漏水事故を誘発するであろう
。Any water system can be dangerous if the water pipe material is not corrosion resistant and is not protected against corrosion. In a circulating cooling water system such as an air conditioning system, the cooling water is circulated and reused, and it is also a general management method to suppress the amount of blow water, resulting in concentration of the cooling water and an increase in salt concentration. As a result, scale and suspended solids are deposited on the wall surface, and corrosion of the metal is increased due to this, and scale damage and corrosion damage are likely to occur. Scale and the like that adhere to the heat conductive surfaces of equipment heat exchangers and the like may cause a decrease in heat exchange efficiency and may lead to cracking or high pressure cuts. Rust lumps in pipes may cause blockages and water leaks.
本発明者等は脂肪族オキシカルボン酸若しくけその塩、
ベンゾトリアゾール類及びケイ酸アルカリ塩を併用する
ことにより著しく優れた防食作用の得られることを知っ
た。更に、これらにポリアクリル酸若しくはその塩を併
用すると一段と防食作用が増強されることを知った。The present inventors have developed a salt of an aliphatic oxycarboxylic acid or a salt thereof,
It has been found that by using benzotriazoles and alkali silicates in combination, an extremely excellent anticorrosion effect can be obtained. Furthermore, it has been found that when polyacrylic acid or its salt is used in combination with these, the anticorrosion effect is further enhanced.
ここに本発明は脂肪族オキシカルボン酸若しくけその塩
、ベンゾトリアゾール類及びティ酸アルカリ塩を含有す
ることを特徴とする特許薬剤、及びこれに更にポリアク
リル酸若しくはその塩を含有せしめてなる水処理薬剤に
関する。The present invention provides a patented drug characterized by containing an aliphatic oxycarboxylic acid or a salt thereof, a benzotriazole, and an alkali salt of thiic acid, and a patented drug which further contains polyacrylic acid or a salt thereof. Regarding water treatment chemicals.
本発明で使用するこ七のできる脂肪族オキシカルボン酸
若しく岐その塩は、水溶性のものであって、そのキレー
ト作用から金属の防食剤の−Fi、分として使用が知ら
れているものを含み、例tはグルコン酸、クエン酸、リ
ンゴ酸、酒石酸、乳酸、グリコール酸を代表例として示
すことができる。塩としては、ナトリウム塩、カリウム
塩が好例である。なお、これらオキシカルボン酸の防食
作用は、単独では実用的に使用できる程には強くないこ
とが知られている。The aliphatic oxycarboxylic acid or its salt used in the present invention is water-soluble and is known to be used as a -Fi, anti-corrosion agent for metals due to its chelating action. Examples include gluconic acid, citric acid, malic acid, tartaric acid, lactic acid, and glycolic acid as representative examples. Good examples of salts include sodium salts and potassium salts. It is known that the anticorrosion effect of these oxycarboxylic acids alone is not strong enough to be used for practical purposes.
本発明で使用することのできる代表的インシトリアゾー
ル類は、一般式(I):
(式中、Xけ水素原子、低級アルキル基、カルボキシル
基、アルコキシカルボニル基を衷わり、Mけ水素原子t
たけアルカリ金属を示す)
で表わされる水溶性の化合物で、これらは銅系金属の防
食剤として公知である。しかし、これらには鉄の防食作
用はない。Typical incitriazoles that can be used in the present invention have the general formula (I): (wherein,
These are water-soluble compounds represented by the following formula (indicating an alkali metal), and are known as anticorrosive agents for copper-based metals. However, these do not have the anticorrosion effect of iron.
一ト記一般弐〇)で表わされる化合物の代表例としては
次のものを示すことができる(そのアルカリ金属塩を含
tr):
IH−ベンゾトリアゾール、4−メチル〜IH−・ベン
ゾトリアゾール、5−メチル−IH−ベンゾトリアゾー
ル、4−カルボキシ−IH−ベンゾトリアゾール、4−
ブトキシカルボニル−IH−ベンゾトリアゾール
これらのアルカリ金属塩としてはナトリウム塩、カリウ
ム塩が好例である。Typical examples of the compounds represented by Itoki General 2〇) include the following (including their alkali metal salts): IH-benzotriazole, 4-methyl to IH-benzotriazole, 5 -Methyl-IH-benzotriazole, 4-carboxy-IH-benzotriazole, 4-
Butoxycarbonyl-IH-benzotriazole Examples of alkali metal salts thereof include sodium salt and potassium salt.
本発明で使用するときのできるケイ酸アルカリ塩として
は、例えばケイ酸ソーダ、メタケイ酸ソーダ、ケイ酸カ
リウム等を挙げることができZo
tた本発明で使用することのできるポリアクリル#若し
くけその蝮としては平均分子量が20、 nn0N度若
しくけそれ以下の水溶性若しくけ水に容易に分散しつる
性質を有する也の(補助剤の助けを借りれば分散しつる
ものを含む)を挙げることができる。代表的なものとし
て岐ポリアクリル酸ソーダがある。このような重合体が
炭酸カルシウム系スケールの分散作用(スケールの付着
抑制作用)を有することは知られているがその効果は弱
く、単独で使用されることけ少ない。Examples of the alkali silicate salts that can be used in the present invention include sodium silicate, sodium metasilicate, potassium silicate, and the like. The vipers include those that have an average molecular weight of 20, nn0N degrees or less and are water-soluble or have the property of easily dispersing in water and exhibiting vine properties (including those that can be dispersed and vine with the aid of adjuvants). can be mentioned. A typical example is sodium polyacrylate. Although such polymers are known to have a calcium carbonate scale dispersion effect (scale adhesion inhibiting effect), this effect is weak and they are rarely used alone.
本発明によれば、上記した脂ff/j族メキシカルボン
耐若しくけその均、ベンゾトリアゾ−ル類乃びケイ酸ア
ルカリ塩を併用することにより、鉄系71ひ銅系金属を
迎水部に使用する通水系統の腐食防止・スケールハjノ
止及び懸濁物の付着防II−等に優れた効果が得られる
。史に本発明によれば、上記成分に更にポリアクリル酸
若しくはその塩を併用することにより腐食防]ト効来が
一段と安定化きれ増強される。本発明にむける典型的な
処方でrL1上記した各成分が水溶性乃至氷水に分散性
結晶であるものが使用されるので、この場合、!発明組
成物は71(溶液の形tたは使用に都合のよい大きさに
粉末若しくけっぷ状とした形で提供される。上記各成分
を混合物とするに際しての配1合比は製品中、脂肪族オ
キシカルボン酸若しくはその塩を5〜30%(重量比。According to the present invention, iron-based 71-arsenic metal is added to the water receiving part by using the above-mentioned fatty acid ff/J group mexicarboxylic acid, benzotriazole, and alkali silicate. Excellent effects can be obtained in preventing corrosion, scaling, and adhesion of suspended matter in the water flow system used. According to the present invention, the anti-corrosion effect is further stabilized and enhanced by further adding polyacrylic acid or a salt thereof to the above-mentioned components. In a typical formulation for the present invention, rL1 each of the above-mentioned components is used in the form of water-soluble or ice-water dispersible crystals, so in this case,! The composition of the invention can be provided in the form of a solution or in the form of a powder or powder in a size convenient for use. , 5 to 30% (weight ratio) of aliphatic oxycarboxylic acid or its salt.
以下同じ)、ベンゾトリアゾール類を1〜10%、ケイ
酸アルカリ塩を5〜30%の範囲から適宜に選択すれば
よいが、水溶液として組成する場合、溶媒としての水に
溶解し、かつ水溶液の形で製品を得ることができる範囲
から選択せねばならないことはいうまでもない。ポリア
クリル酸若しくはその塩の配合割合は、製品中、5〜3
0%の範囲から選べばよい。(same below), benzotriazoles in 1 to 10%, and alkali silicate in 5 to 30%. However, when forming an aqueous solution, it is necessary to dissolve it in water as a solvent and to form an aqueous solution. It goes without saying that the choice must be made from within the range in which the product can be obtained. The blending ratio of polyacrylic acid or its salt is 5 to 3 in the product.
You can choose from a range of 0%.
本発明の水処理剤は、通水系統中での本発明薬剤の全薬
効成分量が通常概そ20〜500ppm好ましくは40
〜J1111 ppmとなるように、処理すべき通水系
統に添加Φ処理される。効果の確実を期すためとかまた
水温が例えば500c 近辺若しくdそれ取上と繁るよ
うな高温通水系統では上記4度域のうち高y弗度とする
のが都合よい〇例えば全薬効成分量として50〜5nO
ppmの範囲での似i用が望ましい○
実験例1
斬鋼試験片
規 格 88−.41
大きさ 50 mm X30 mm X 1 mm、上
部に径3mmの孔をあけている。 31.6 cm2
前処理 軟鋼片は常法により前処理した。すなわち、石
油ベンジン中に1日1丈ト浸漬してH辱財し、IM−N
aOH中に9000で加分間浸漬し、蒸留水で水洗し、
30蟹HO1中に1分間、20%器03中に20秒間、
更に30奮HO1中に1分間浸漬険のち蒸留水、メタノ
ールの順で洗浄し乾燥させ精秤し供試しな。In the water treatment agent of the present invention, the total amount of the medicinal ingredients of the present agent in the water system is usually approximately 20 to 500 ppm, preferably 40 ppm.
It is added to the water flow system to be treated so that it becomes ~J1111 ppm. In order to ensure the effectiveness, and in high-temperature water flow systems where the water temperature is around 500C or more frequently, it is convenient to use a high y-fluidity within the above 4 degree range. For example, the total amount of medicinal ingredients. as 50~5nO
It is desirable to use a similar material in the ppm range ○ Experimental Example 1 Cutting Steel Test Piece Standard 88-. 41 Size: 50 mm x 30 mm x 1 mm, with a hole 3 mm in diameter at the top. 31.6 cm2 Pretreatment The mild steel pieces were pretreated by a conventional method. In other words, IM-N was immersed in petroleum benzine for one length a day to be humiliated.
Soaked in aOH for 9000 min, rinsed with distilled water,
30 crab in HO1 for 1 minute, 20% in vessel 03 for 20 seconds,
After immersing for 1 minute in 30% HO1, wash with distilled water and methanol in that order, dry, weigh accurately, and test.
実一方法
大阪市水に供試薬剤を所定4度となるように添加し全景
を51111 rr+lとし、所定の水温に保つ〇前処
理済の@構試験片をカシーー塗料で褪覆したピアノ線で
L記溶液中につるし浸漬した。Practical method: Add the test chemical to Osaka city water at a predetermined temperature of 4 degrees, make the overall view 51111 rr+l, and keep the water at the predetermined temperature. A pretreated @structure test piece was coated with a piano wire covered with Cassie paint. It was suspended and immersed in the solution described above.
7R液はスタラーで攪拌しく 、4(111rpm)、
また試験期間中に蒸発する水分は適宜大阪市水で補給し
た。試験片上の腐食生成物は歯ぶらして荒おとししたの
ち、インヒビターとして1%プロパルギルアルコールを
含ムlo%HC/溶液に浸漬して除去する。試験片を秤
量して、腐食速度及び防食率を算出した。結果を次表に
示す。Stir the 7R liquid with a stirrer, 4 (111 rpm),
In addition, water that evaporated during the test period was replenished with Osaka city water as appropriate. Corrosion products on the test piece are removed by brushing and then immersed in a 1% HC/solution containing 1% propargyl alcohol as an inhibitor. The test piece was weighed and the corrosion rate and corrosion protection rate were calculated. The results are shown in the table below.
△W:試験前後の重量減(mg)
S:面積(4m2)
J):l耳間(日)
条件 水温25°C±0.200
浸漬時間 48時間
大阪市水分析値
MS:メタケイ酸ソーダ
BT:IH−ベンゾトリアゾール
実験例2
実施1+lI2処方の水処理薬剤につき(1)液温5±
02°C及び(2+42 ” 0.5°Cにて実撃例1
の方法に準じて腐食抑制効果試験をおこなった。結果は
次表に示す。尚、表中のう麻(ppm)け極刑としての
濃度(ppm)である。△W: Weight loss before and after test (mg) S: Area (4m2) J): Between ears (days) Conditions Water temperature 25°C ± 0.200 Immersion time 48 hours Osaka city water analysis value MS: Sodium metasilicate BT :IH-Benzotriazole Experimental Example 2 For water treatment agent of Example 1+lI2 formulation (1) Liquid temperature 5±
Actual shot example 1 at 0.02°C and (2+42” 0.5°C)
A corrosion inhibition effect test was conducted according to the method described in . The results are shown in the table below. Note that the concentration (ppm) in the table is the maximum concentration (ppm).
1)液温(1)のとき
2)液温(2)のとき
実験例3
実施例3処方の水処理薬剤につき液渇関±0.200に
て実験例1の方法に準じて腐食抑制効果試験をおこ寿っ
た。結果は次表に示す0尚、表中の一度(p pm )
は製剤としての4度(ppm)である。1) When the liquid temperature is (1) 2) When the liquid temperature is (2) Experimental example 3 Corrosion inhibition effect according to the method of Experimental example 1 at liquid drying ratio ±0.200 for the water treatment agent prescribed in Example 3 I passed the exam. The results are shown in the following table.
is 4 degrees (ppm) as a formulation.
実験例4
実施例3処方の水処理薬剤を使用して隼ビル蓄熱槽にて
腐食抑制効果の現場実験をおこなった。N質SS−,4
1の軟鋼試験片をつり糸で2ケ所に浸漬した。その他は
実1・湧例1の方法に準じた。Experimental Example 4 Using the water treatment agent formulated in Example 3, an on-site experiment was conducted on the corrosion inhibiting effect in the Hayabusa Building heat storage tank. N quality SS-, 4
The mild steel test piece of No. 1 was dipped in two places with a hanging string. Other procedures followed the methods of Example 1 and Example 1.
条件 集ビル蓄熱槽の保有水量 約40トン水温 55
〜60°C
実験胡m121日間
g1g剤添加fd 2A)kg(Hそ500p pm
)水質
色度 12
pH8,6(2000)
(0/−’:l 26.’ my/ /IC8od 1
47.8mg//
鉄 0.11 mg/l
銅 0.02mg/IJ
亜鉛 0.02mg/1
(Si02) 192mg/l
総アルカリ度 71.8 mg/l
全硬度 111 mg#’
導電率 396 μ/cm
結果を次表に示す。尚、表中の4度(ppm)は薬剤と
しての濃度rppm)である。Conditions Amount of water held in the building heat storage tank Approximately 40 tons Water temperature 55
~60°C Experimental heat 121 days G1g agent addition fd 2A) kg (H so 500p pm
) Water chromaticity 12 pH8,6 (2000) (0/-':l 26.' my/ /IC8od 1
47.8mg// Iron 0.11 mg/l Copper 0.02mg/IJ Zinc 0.02mg/1 (Si02) 192mg/l Total alkalinity 71.8 mg/l Total hardness 111 mg#' Electrical conductivity 396 μ/ cm The results are shown in the table below. In addition, 4 degrees (ppm) in the table is the concentration as a drug (ppm).
参考例
実挽例1の方法に準じて、表中の薬剤について、防食性
を調べた。Reference Example According to the method of Milling Example 1, the anticorrosion properties of the chemicals listed in the table were investigated.
条件 関±0.580 浸漬時間240時間次に実噛例
の若干を示すが、成分の神類・割合は本発明の1憤囲内
で変財させうるものであることは勿−である。Conditions: ±0.580 Soaking time: 240 hours Next, some actual chewing examples will be shown, but it goes without saying that the quality and proportion of the ingredients can be changed within the scope of the present invention.
′ρ1・巾例1
ポリアクリ馴酸ソーダ(J1%WoカヤクリルレジンH
−35N)2F1%メタケイ酸ソーダ 5%
グルコン酸ソーダ 5%
1)4−ベンゾトリアゾール 1%を
水 69%に
均一にン容解してなる水処理薬剤。'ρ1 Width Example 1 Polyacrylic Sodium (J1%Wo Kayacrylic Resin H
-35N) 2F 1% Sodium metasilicate 5% Sodium gluconate 5% 1) A water treatment agent prepared by uniformly dissolving 1% 4-benzotriazole in 69% water.
本本処理薬剤は、冷711A水系続の金属の腐食防止の
なめに使用される。This treatment agent is used to prevent corrosion of metals in cold 711A water systems.
実ず也例2
ポリアクリル学ソーダ(40%情。カヤクリルレジンI
”lイ個N) 20%メタケイ酢ソーダ 10%
0%グルコン酸ソーダ 5%
114−ベンゾトリアゾール 1%を
水 64%に
均一に溶解してなる水処理薬剤。Mizuya Example 2 Polyacrylic Soda (40%) Kayacrylic Resin I
A water treatment agent made by uniformly dissolving 20% sodium silica vinegar 10% 0% sodium gluconate 5% 114-benzotriazole 1% in 64% water.
本水処理薬剤は、冷Δ、λ水系統の金属の腐食防【(−
のために使用される。This water treatment agent is used to prevent corrosion of metals in cold Δ and λ water systems [(−
used for.
実I布例3
ポリアクリ4ソーダ(40%品カヤクリルレジン■(−
3FN)2I)%メタケイ酸ソーダ 5%
グルコン酸ソーダ 10イ
11−T−ベンゾトリアゾール 1イを水 64%に
均一に溶解してなる水処理薬剤。Actual I fabric example 3 Polyacrylic 4 soda (40% product Kayacrylic resin ■ (-
3FN) 2I)% Sodium metasilicate 5% Sodium gluconate 10I 11-T-benzotriazole 1I A water treatment agent prepared by uniformly dissolving 1I in 64% water.
Claims (1)
トリアゾール類及びケイ酸アルカリ塩を含有することを
特徴とする水処理薬剤0(2)脂肪族オキシカルボン酸
若しくはその塩、ベンゾトリアゾール類、ケイ酸アルカ
リ塩及びポリアクリル酸若しくはその塩を含有すること
を特徴とする水処理薬剤0(1) A water treatment agent characterized by containing an aliphatic oxycarboxylic acid or its salt, benzotriazoles and an alkali silicate salt (2) an aliphatic oxycarboxylic acid or its salt, benzotriazoles, Water treatment agent 0 characterized by containing an alkali silicate salt and polyacrylic acid or its salt
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9629983A JPS6086286A (en) | 1983-05-31 | 1983-05-31 | Water treating chemical agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9629983A JPS6086286A (en) | 1983-05-31 | 1983-05-31 | Water treating chemical agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6086286A true JPS6086286A (en) | 1985-05-15 |
| JPH0140915B2 JPH0140915B2 (en) | 1989-09-01 |
Family
ID=14161153
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9629983A Granted JPS6086286A (en) | 1983-05-31 | 1983-05-31 | Water treating chemical agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6086286A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996017033A1 (en) * | 1994-11-25 | 1996-06-06 | Buna Sow Leuna Olefinverbund Gmbh | Nitrite-, phosphate- and amine-free coolant and heat-transfer agent |
| EP0807695A1 (en) * | 1996-05-15 | 1997-11-19 | Nalco Chemical Company | A non-phosphorus corrosion inhibitor for industrial cooling water systems and airwasher systems |
| JP2002018487A (en) * | 2000-07-10 | 2002-01-22 | Miura Co Ltd | Water treatment method for boiler system |
| CN105036363A (en) * | 2015-07-13 | 2015-11-11 | 鞍钢贝克吉利尼水处理有限公司 | Composite corrosion inhibitor suitable for desalted water and preparation method |
| JP2015213851A (en) * | 2014-05-07 | 2015-12-03 | 伯東株式会社 | Water treatment composition and water treatment method |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53123343A (en) * | 1977-04-01 | 1978-10-27 | Mogul Corp | Corrosion inhibiting component and its use method |
-
1983
- 1983-05-31 JP JP9629983A patent/JPS6086286A/en active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53123343A (en) * | 1977-04-01 | 1978-10-27 | Mogul Corp | Corrosion inhibiting component and its use method |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996017033A1 (en) * | 1994-11-25 | 1996-06-06 | Buna Sow Leuna Olefinverbund Gmbh | Nitrite-, phosphate- and amine-free coolant and heat-transfer agent |
| EP0807695A1 (en) * | 1996-05-15 | 1997-11-19 | Nalco Chemical Company | A non-phosphorus corrosion inhibitor for industrial cooling water systems and airwasher systems |
| US5976414A (en) * | 1996-05-15 | 1999-11-02 | Nalco Chemical Company | Non-Phosphorus corrosion inhibitor program for air washer system |
| JP2002018487A (en) * | 2000-07-10 | 2002-01-22 | Miura Co Ltd | Water treatment method for boiler system |
| JP2015213851A (en) * | 2014-05-07 | 2015-12-03 | 伯東株式会社 | Water treatment composition and water treatment method |
| CN105036363A (en) * | 2015-07-13 | 2015-11-11 | 鞍钢贝克吉利尼水处理有限公司 | Composite corrosion inhibitor suitable for desalted water and preparation method |
| CN105036363B (en) * | 2015-07-13 | 2017-03-01 | 鞍钢贝克吉利尼水处理有限公司 | A kind of composite corrosion inhibitor of suitable demineralized water and preparation method |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0140915B2 (en) | 1989-09-01 |
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