JPH0426783A - Corrosion inhibitor for high temperature water system - Google Patents

Corrosion inhibitor for high temperature water system

Info

Publication number
JPH0426783A
JPH0426783A JP12932490A JP12932490A JPH0426783A JP H0426783 A JPH0426783 A JP H0426783A JP 12932490 A JP12932490 A JP 12932490A JP 12932490 A JP12932490 A JP 12932490A JP H0426783 A JPH0426783 A JP H0426783A
Authority
JP
Japan
Prior art keywords
tannic acid
tannate
temperature water
corrosion inhibitor
water
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
JP12932490A
Other languages
Japanese (ja)
Other versions
JP2845572B2 (en
Inventor
Toshiharu Wake
敏治 和気
Yoshiaki Shibata
芳昭 柴田
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.)
Organo Corp
Original Assignee
Organo Corp
Japan Organo Co 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 Organo Corp, Japan Organo Co Ltd filed Critical Organo Corp
Priority to JP12932490A priority Critical patent/JP2845572B2/en
Publication of JPH0426783A publication Critical patent/JPH0426783A/en
Application granted granted Critical
Publication of JP2845572B2 publication Critical patent/JP2845572B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Abstract

PURPOSE:To provide the title inhibitor ensuring safety, hardly increasing electrical conductivity and having superior corrosion inhibiting ability by blending tannic acid and/or tannate with a reducing phenol compd. in a prescribed ratio. CONSTITUTION:Tannic acid and/or water soluble tannate such as sodium tannate is blended with a reducing phenol compd. such as gallic acid preferably in about (8:2)-(4:6) weight ratio to prepare the title inhibitor. This inhibitor ensures high safety because of no hydrazine content, has superior corrosion inhibiting ability and can reduce the amt. of a blow because it does not increase the electrical conductivity of water.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明はボイラ、熱水系等の高温水系腐食抑制剤に関す
る。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a corrosion inhibitor for high-temperature water systems such as boilers and hydrothermal systems.

〈従来の技術〉 従来からボイラ缶内あるいは加熱または冷却循環系等の
高温水系腐食抑制方法として脱酸素剤とアルカリ剤を併
用添加することが行われており、当該脱酸素剤としては
ヒドラジンまたは亜硫酸ナトリウムが主として使用され
ている。またタンニン酸あるいはその塩も一部使用され
ている。
<Prior art> Conventionally, as a method of suppressing corrosion in high-temperature water systems such as inside boiler cans or in heating or cooling circulation systems, oxygen scavengers and alkaline agents have been added in combination. Sodium is mainly used. Tannic acid or its salts are also used in some cases.

〈発明が解決しようとする問題点〉 近年、水処理薬品に対する安全性、またそれを使用する
ことによる省エネルギー効果に関心が高まっており高温
水系腐食抑制剤もその例外ではない。しかしながらヒド
ラジンは毒性があり安全性の点で問題があるため、発生
した蒸気、高温水が直接に人体、製品に接触する可能性
がある病院、食品工場等では使用できない。また亜硫酸
ナトリウムは安全性は問題ないが使用量が多く電気伝導
率を上昇させるためブロー量が上昇し、水、燃料の使用
量が多くなる結果、エネルギーコストが増大するばかり
でなく、酸素との反応生成物(硫酸イオン)が腐食因子
となり十分な腐食抑制効果を発揮しない。またタンニン
酸あるいはその塩は安全性は問題ないが単独では特に初
期において十分な腐食抑制効果を発揮しない。
<Problems to be Solved by the Invention> In recent years, there has been increasing interest in the safety of water treatment chemicals and the energy-saving effect of using them, and high-temperature water-based corrosion inhibitors are no exception. However, hydrazine is toxic and has safety issues, so it cannot be used in hospitals, food factories, etc. where the generated steam and high-temperature water may come into direct contact with the human body or products. Furthermore, although there is no safety issue with sodium sulfite, the amount used is large and increases the electrical conductivity, which increases the amount of blowing, which increases the amount of water and fuel used, which not only increases energy costs, but also increases the amount of water and fuel used. The reaction product (sulfate ion) becomes a corrosion factor and does not exhibit sufficient corrosion inhibition effect. Furthermore, although tannic acid or its salt has no safety problems, when used alone it does not exhibit a sufficient corrosion inhibiting effect, especially in the initial stage.

本発明は、これら従来方法の有する問題点を解決するも
ので、安全性に問題がなく、電気伝導率の上昇が低く優
れた腐食抑制効果を発揮する高温水系腐食抑制剤を提供
することを目的とする。
The present invention solves the problems of these conventional methods, and aims to provide a high-temperature water-based corrosion inhibitor that has no safety problems, exhibits a low increase in electrical conductivity, and exhibits an excellent corrosion inhibiting effect. shall be.

く問題点を解決するための手段〉 上記目的を達成するためになされた本発明よりなる高温
水系腐食抑制剤はタンニン酸およびまたはタンニン酸塩
と還元性フェノール化合物を含むことを特徴とするもの
である。
Means for Solving the Problems> The high-temperature water-based corrosion inhibitor according to the present invention, which has been made to achieve the above object, is characterized by containing tannic acid and/or a tannic acid salt and a reducing phenol compound. be.

本発明で使用されるタンニン酸は柿、茶、五倍子等の植
物から抽出されるポリフェノール化合物であり、加水分
解性タンニス縮台型タンニンに分類されるがいずれを使
用しても良い。
The tannic acid used in the present invention is a polyphenol compound extracted from plants such as persimmon, tea, and quince, and is classified as a hydrolyzable tannis-type tannin, but any of them may be used.

本発明で使用されるタンニン酸塩は上述のタンニン酸の
ナトリウム塩、カリウム塩のような水溶性塩を指す。
The tannic acid salt used in the present invention refers to water-soluble salts such as the above-mentioned sodium and potassium salts of tannic acid.

また本発明で使用される還元性フェノール化合物として
は天然物由来の没食子酸、ピロガロール、タロロゲン酸
、キナ酸、カフェ酸、クマール酸、シンナム酸、トコフ
ェロール等の還元性フェノール化合物の酸およびその塩
があり、これらのものの一つ以上を使用できる。
In addition, the reducing phenolic compounds used in the present invention include acids and salts thereof of reducing phenolic compounds such as gallic acid, pyrogallol, talologenic acid, quinic acid, caffeic acid, coumaric acid, cinnamic acid, and tocopherol derived from natural products. Yes, you can use one or more of these.

本発明の高温水系腐食抑制剤は(1)タンニン酸と還元
性フェノール化合物、 (2)タンニン酸塩と還元性フ
ェノール化合4N(3)タンニン酸とタンニン酸塩と還
元性フェノール化合物、の上記(1)、 (2)、 (
3)のいずれかを必須とするもので、 (3)のタンニ
ン酸とタンニン酸塩の両者を用いる場合、その混合比は
任意である。また上述の(1)、 (2)、 (3)共
通してタンニン酸およびまたはタンニン酸塩と還元性フ
ェノール化合物は重量比で9= 1ないし2:8、好ま
しくは8:2ないし4:6の範囲で使用する。各々を上
記の割合で別々に添加しても良いし、上記の割合で予め
配合して使用しても良い。なおタンニン酸あるいはタン
ニン酸塩を高アルカリ溶液に溶解(タンニン酸を用いた
場合、溶解直後にタンニン酸塩となる)し、これを放置
するとタンニン酸塩の一部が分解して還元性フェノール
である没食子酸あるいはピロガロールを生成する性質が
ある。
The high-temperature water-based corrosion inhibitor of the present invention comprises (1) tannic acid and a reducing phenol compound, (2) a tannic acid salt and a reducing phenol compound 4N, and (3) tannic acid, a tannic acid salt and a reducing phenol compound. 1), (2), (
Either one of 3) is essential, and when both tannic acid and tannate salt of (3) are used, the mixing ratio is arbitrary. Furthermore, in common with the above (1), (2), and (3), the weight ratio of tannic acid and/or tannate salt to the reducing phenol compound is 9=1 to 2:8, preferably 8:2 to 4:6. Use within the range. Each may be added separately in the above proportions, or may be mixed in advance in the above proportions before use. Note that if tannic acid or tannate salts are dissolved in a highly alkaline solution (if tannic acid is used, it becomes tannate salts immediately after dissolution) and left to stand, part of the tannate salts will decompose and form reducing phenols. It has the property of producing certain gallic acid or pyrogallol.

従って本性質を積極的に利用して、タンニン酸あるいは
タンニン酸塩を高アルカリ溶液に溶解しこれを放置する
ことによりタンニン酸塩と還元性フェノールが混合され
ている本発明の高温水系腐食抑制剤を製造する事もでき
る。
Therefore, the high-temperature water-based corrosion inhibitor of the present invention actively utilizes this property to mix tannic acid or a tannic acid salt with a reducing phenol by dissolving the tannic acid or tannic acid salt in a highly alkaline solution and leaving it to stand. It is also possible to manufacture

タンニン酸およびまたはタンニン酸塩と還元性フェノー
ル化合物の使用量は前記重量比で配合されたそれぞれの
物質の合計の水中の濃度で30ないし1000mg/ 
Iが適当である。
The amount of tannic acid and/or tannate salt and reducing phenol compound to be used is 30 to 1000 mg/concentration in water of the total of each substance blended in the above weight ratio.
I is appropriate.

発明で言う高温水とは40℃以上200℃以下の水を言
い、これらの水温を有する加熱循環系あるいはボイラ水
系の防食に本薬剤は使用できる。
The high-temperature water referred to in the invention refers to water at a temperature of 40° C. or higher and 200° C. or lower, and the present agent can be used for corrosion protection of heating circulation systems or boiler water systems having these water temperatures.

また本発明の腐食抑制剤は水酸化ナトリウム、炭酸ナト
リウムの様なpH調整斉L りん酸ナトリウム、ヘキサ
メタりん酸ナトリウムの様なリン酸塩、ポリアクリル酸
ナトリウム、ポリマレイン酸ナトリウムの様な分散剤お
よびオクタデシルアミン、シクロヘキシルアミンの様な
蒸気系腐食抑制剤と併用したり、配合し使用する事は何
ら差し支えない。
The corrosion inhibitors of the present invention may also include pH adjusting agents such as sodium hydroxide and sodium carbonate; phosphates such as sodium phosphate and sodium hexametaphosphate; dispersants such as sodium polyacrylate and sodium polymaleate; There is no problem in using it in combination or in combination with steam-based corrosion inhibitors such as octadecylamine and cyclohexylamine.

く作用〉 タンニン酸およびまたはタンニン酸塩は脱酸素能力だけ
でなく金属表面への防食皮膜形成、金属表面の不動態化
作用により金属に対し優れた腐食抑制能力を発揮するが
、酸素との反応速度は必ずしも速いとは言えず単独では
添加初期の脱酸素効果が不十分であり、したがって添加
初期の腐食抑制効果が十分でない。
Tannic acid and/or tannate salts not only have oxygen scavenging ability, but also have excellent corrosion inhibiting ability on metals by forming an anticorrosion film on the metal surface and passivating the metal surface, but they do not react with oxygen. The speed is not necessarily high, and when added alone, the deoxidizing effect at the initial stage of addition is insufficient, and therefore the corrosion inhibiting effect at the early stage of addition is not sufficient.

一方還元性フエノール化合物は酸素との反応速度は非常
に速いものの防食皮膜形成、不動態化作用は小さい。
On the other hand, reducing phenol compounds have a very fast reaction rate with oxygen, but their anticorrosive film formation and passivation effects are small.

再化合物を上記の割合および量で使用する事によりタン
ニン酸およびまたはタンニン酸塩のみを使用した場合に
見られる初期の腐食抑制力の低下を還元性フェノール化
合物の優れた脱酸素能力で補い、さらにタンニン酸およ
びまたはタンニン酸塩と還元性フェノール化合物の存在
により金属表面にタンニン酸およびまたはタンニン酸塩
のみでは形成不可能な安定した緻密な防食皮膜を形成す
るという相乗効果により優れた腐食抑制効果を発揮する
ものと考えられる。
By using the re-compound in the above ratio and amount, the reduction in initial corrosion inhibiting power seen when using only tannic acid and/or tannate salts can be compensated for by the excellent oxygen scavenging ability of the reducing phenolic compound, and The presence of tannic acid and/or tannate salts and a reducing phenol compound creates an excellent corrosion inhibiting effect due to the synergistic effect of forming a stable and dense anti-corrosion film on the metal surface that cannot be formed with tannic acid and/or tannate salts alone. It is thought that this will be effective.

以下に本発明の詳細な説明する。The present invention will be explained in detail below.

実施例1 実験用ボイラに軟鋼製テストチューブ(内径50mm、
 長さ500mm)、軟鋼製テストピース(20x50
x2mm)を設置し、軟水、薬剤を自動補給しながら下
記の条件で150時間連続運転を行っt島 運転条件 ボイラ圧力;   10kg/crri’−Gブロー%
 ・  10% ボイラ水質(平均): pH;11,3 塩化物イオン;  255mgCl/IMアルカリ度;
  630mgCaC0a/IPアル力リ度;  51
0mgCaCOg/lりん酸イオン;   37mgP
Oa/1試験終了後テストチューブ、テストピースを取
り出しテストチューブについては表面観察、テストピー
スについては腐食度を次式により測定した。
Example 1 A mild steel test tube (inner diameter 50 mm,
length 500mm), mild steel test piece (20x50
x 2 mm) was installed and operated continuously for 150 hours under the following conditions while automatically replenishing soft water and chemicals. T island operating conditions Boiler pressure: 10 kg/crri'-G blow %
・10% Boiler water quality (average): pH; 11.3 Chloride ion; 255mgCl/IM alkalinity;
630mgCaC0a/IP strength; 51
0mgCaCOg/l phosphate ion; 37mgP
After the Oa/1 test was completed, the test tube and test piece were taken out, and the surface of the test tube was observed, and the degree of corrosion of the test piece was measured using the following formula.

試験結果を表1に示しtも 表1 表1より本発明の腐食抑制剤が優れた効果を発揮するこ
とがわかる。
The test results are shown in Table 1, and t is also shown in Table 1.Table 1 shows that the corrosion inhibitor of the present invention exhibits excellent effects.

実施例−2 イオン交換水(電気伝導率0.6μS/crrr)に亜
硫酸ナトリウムおよび本発明の高温水系腐食抑制剤(タ
ンニン酸と没食子酸の重量比7: 3)を順次添加して
その電気伝導率の変化を測定した。
Example 2 Sodium sulfite and the high-temperature water-based corrosion inhibitor of the present invention (weight ratio of tannic acid and gallic acid 7:3) were sequentially added to ion-exchanged water (electrical conductivity 0.6 μS/crrr) to improve its electrical conductivity. The change in rate was measured.

試験結果を表2に示す。The test results are shown in Table 2.

表2 表2より本発明の腐食抑制剤の添加による電気伝導率の
上昇は亜硫酸ナトリウムと比較して非常に少ない。従っ
て高温水系において電気伝導率をある値以下に維持する
ために行うブロー量の削減につながり省エネルギーに貢
献する。
Table 2 From Table 2, the increase in electrical conductivity due to the addition of the corrosion inhibitor of the present invention is very small compared to sodium sulfite. Therefore, in high-temperature water systems, the amount of blowing required to maintain electrical conductivity below a certain value can be reduced, contributing to energy savings.

〈効果〉 以」二説明したごとく本発明の高温水系腐食抑制剤はヒ
ドラジンを用いてないので安全性が高く、かつ優れた腐
食抑制能力を有するとともに、水の電気伝導率を上昇さ
せることがないので、ブロー量の削減につながり省エネ
ルギーに貢献し、産業に与える利益は大きい。
<Effects> As explained in Section 2, the high temperature water-based corrosion inhibitor of the present invention does not use hydrazine, so it is highly safe, has excellent corrosion inhibiting ability, and does not increase the electrical conductivity of water. Therefore, it leads to a reduction in the amount of blowing and contributes to energy conservation, which brings great benefits to industry.

手 続 補 正 書 (自発) 平成3年7月5日 特許庁長官  植 松  敏 殿 1、事件の表示 平成2年特許願第129324号 2、発明の名称 高温水系腐食抑制剤 3、補正をする者 事件との関係 特許出願人 〔連絡先〕 〒113 東京都文京区本郷5丁目5番16号 オルガノ株式会社 法務特許部 電話番号03−5689−5115 4、補正の対象 明細書の発明の詳細な説明の欄 明細書中の下記事項を訂正願います。hand Continued Supplementary Positive book (spontaneous) July 5, 1991 Commissioner of the Patent Office Toshi Ue Matsu 1.Display of the incident 1990 Patent Application No. 129324 2. Name of the invention High temperature water based corrosion inhibitor 3. Person who makes corrections Relationship to the incident: Patent applicant 〔contact address〕 〒113 5-5-16 Hongo, Bunkyo-ku, Tokyo Organo Co., Ltd. Legal and Patent Department Phone number 03-5689-5115 4. Subject of correction Detailed description of the invention in the specification Please correct the following items in the statement.

1、第5頁4行目に 「発明で言う」 とあるのを 「本 発明で言う」 と訂正する。1, page 5, line 4 "Invention" There is a certain thing "Book I say it by invention.” I am corrected.

以 」ニBelow ”

Claims (1)

【特許請求の範囲】[Claims]  タンニン酸およびまたはタンニン酸塩と還元性フェノ
ール化合物を含むことを特徴とする高温水系腐食抑制剤
A high-temperature water-based corrosion inhibitor characterized by containing tannic acid and/or a tannic acid salt and a reducing phenol compound
JP12932490A 1990-05-21 1990-05-21 High-temperature water-based corrosion inhibitor Expired - Lifetime JP2845572B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12932490A JP2845572B2 (en) 1990-05-21 1990-05-21 High-temperature water-based corrosion inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12932490A JP2845572B2 (en) 1990-05-21 1990-05-21 High-temperature water-based corrosion inhibitor

Publications (2)

Publication Number Publication Date
JPH0426783A true JPH0426783A (en) 1992-01-29
JP2845572B2 JP2845572B2 (en) 1999-01-13

Family

ID=15006773

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12932490A Expired - Lifetime JP2845572B2 (en) 1990-05-21 1990-05-21 High-temperature water-based corrosion inhibitor

Country Status (1)

Country Link
JP (1) JP2845572B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013124411A (en) * 2011-12-16 2013-06-24 Japan Organo Co Ltd Metal anticorrosive

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013124411A (en) * 2011-12-16 2013-06-24 Japan Organo Co Ltd Metal anticorrosive

Also Published As

Publication number Publication date
JP2845572B2 (en) 1999-01-13

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