JPS63166981A - Aqueous composite antiscale agent for boiler - Google Patents

Aqueous composite antiscale agent for boiler

Info

Publication number
JPS63166981A
JPS63166981A JP31282186A JP31282186A JPS63166981A JP S63166981 A JPS63166981 A JP S63166981A JP 31282186 A JP31282186 A JP 31282186A JP 31282186 A JP31282186 A JP 31282186A JP S63166981 A JPS63166981 A JP S63166981A
Authority
JP
Japan
Prior art keywords
boiler
agent
calcium
aqueous composite
catalyst
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
JP31282186A
Other languages
Japanese (ja)
Other versions
JPH0141708B2 (en
Inventor
Junichi Nakajima
純一 中島
Kunio Ochi
越智 邦夫
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.)
Miura Co Ltd
Original Assignee
Miura 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 Miura Co Ltd filed Critical Miura Co Ltd
Priority to JP31282186A priority Critical patent/JPS63166981A/en
Publication of JPS63166981A publication Critical patent/JPS63166981A/en
Publication of JPH0141708B2 publication Critical patent/JPH0141708B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Abstract

PURPOSE:To produce an aqueous composite antiscale agent which effectively prevent the corrosion of a boiler and the sticking of scales by compounding it with the specific ratio of a specified deoxidizer and a catalyst thereof, scale dispersing agent and catalytic promoter for the prevention of chelating. CONSTITUTION:15-30wt.% sulfite as the deoxidizer, 0.003-0.01wt.% cobalt salt as the catalyst, 2-5wt.% sodium polyacrylate (1,000-5,000mol.wt) as a scale dispersing agent and 2-4wt.% nitrate of calcium or magnesium as the catalytic promoter for the prevention of the chelating of polyacrylic acid and cobalt are compounded to prepare the aqueous composite antiscale agent. The corrosion of the boiler and the sticking of the scales can be effectively prevented by using the antiscale agent.

Description

【発明の詳細な説明】 [発明の利用分野] この発明は、ボイラー用複合清缶剤に関するものである
DETAILED DESCRIPTION OF THE INVENTION [Field of Application of the Invention] This invention relates to a composite boiler cleaning agent.

[従来技術] ボイラーの高効率化にともなってボイラーの腐食やスケ
ールの付着などの水質を原因とする問題が複雑になって
きている。
[Prior Art] As boilers become more efficient, problems caused by water quality, such as boiler corrosion and scale adhesion, are becoming more complex.

従来、ボイラー缶内の温度や濃縮度は、どの部位でも同
じものとして水処理が行われてきたが、貫流ボイラーの
様な小型高効率ボイラーにj>いては、給水が流入する
部位と蒸気が排出される部位の温度・濃縮度に大きな差
があり、複雑な症状が現われている。つまり、給水流入
部では、温度が低いために脱酸素力が十分働らかず、低
温腐食が発生しやすく伝熱面においては濃縮度が高いた
めに、スケールが付着しやすい。
Conventionally, water treatment has been carried out assuming that the temperature and concentration inside the boiler can are the same at all parts, but in small, high-efficiency boilers such as once-through boilers, the part where the feed water flows and the part where the steam flows are different. There are large differences in temperature and concentration at the site of excretion, resulting in complex symptoms. In other words, at the feed water inlet, the temperature is low, so the deoxidizing power does not work sufficiently, and low-temperature corrosion is likely to occur, and the heat transfer surface is highly concentrated, so scale is likely to adhere.

従って、低温で速効性せいのある脱酸素剤とともに分散
力の高いスケール分散剤は、どちらも清缶剤にとって不
可欠である。
Therefore, both an oxygen scavenger that acts quickly at low temperatures and a scale dispersant that has high dispersion power are essential for can cleaning agents.

発明者らは、先の研究により低温で効く脱酸素剤として
亜硫酸塩を選び、その触媒としてコバルト塩が有効であ
ることを見いだしたが、この2成分の系に分散剤として
ポリアクリル酸ナトリウムを加えると、ポリアクリル酸
が触媒作用を妨害することがわかった。これは、コバト
イオンとポリアクリル酸のキレート化によるものと考え
られる。
Through previous research, the inventors selected sulfite as an oxygen scavenger that is effective at low temperatures, and found that cobalt salt is effective as a catalyst. When added, polyacrylic acid was found to interfere with catalysis. This is considered to be due to the chelation of cobation and polyacrylic acid.

[発明の概要] そこで、発明者らは、多くの実験・研究を行なった結果
、亜11tI酸塩−コバルト塩−ポリアクリル酸ナトリ
ウムの系にカルシウム又はマグネシウムの塩を加えると
、上記の妨害が防止できることをつきとめた。
[Summary of the Invention] As a result of many experiments and studies, the inventors found that the above-mentioned interference was eliminated by adding a calcium or magnesium salt to the 11tI salt-cobalt salt-sodium polyacrylate system. We found out what can be prevented.

この場合、カルシウムとマグネシウムは共にスケールの
成分であることから、上記の塩の添加によるスケール付
着も予想された。しかし、発明者らの考察によれば、分
子量1 、000〜5,000のナトリウムは自身の濃
度の10倍以上の重im度のスケール成分を溶解する能
力を有しているため、ポリアクリル酸ナトリウムとカル
シウム又はマグネシウムの塩の重量濃度比を1〜1.2
:  1にしておけば、十分にスケールを防止できる。
In this case, since calcium and magnesium are both components of scale, scale adhesion was expected due to the addition of the above-mentioned salt. However, according to the inventors' considerations, sodium with a molecular weight of 1,000 to 5,000 has the ability to dissolve scale components with a weight of more than 10 times its own concentration, so polyacrylic acid The weight concentration ratio of sodium and calcium or magnesium salt is 1 to 1.2.
: If set to 1, scaling can be sufficiently prevented.

尚、カルシウム又はマグネシウムの塩は、6〜iopp
m  as caC’03で十分な効果を発揮するため
、10ppm以下にすることがスケール防止の上からは
好ましい。
In addition, the calcium or magnesium salt is 6 to iopp.
In order to exhibit a sufficient effect at m as caC'03, it is preferable to reduce the amount to 10 ppm or less from the viewpoint of preventing scale.

カルシウムまたはマグネシウムの塩は、一般に溶解度が
低いが、硝酸塩は、溶解度が他の塩に比べて高いので、
清缶剤の成分として硝酸塩を用いるのが良い。また、亜
硫酸塩が低温で速効性のある脱酸素力を持つと、保存安
定性が悪くなるので、安定剤としてソルビン酸カリウム
を用いる(亜硫酸塩に対して重闇比で 1,5%程度)
のが好ましい。
Calcium or magnesium salts generally have low solubility, but nitrates have high solubility compared to other salts, so
It is best to use nitrates as a component of can cleaning agents. In addition, if sulfite has a fast-acting oxygen scavenging ability at low temperatures, storage stability will deteriorate, so potassium sorbate is used as a stabilizer (about 1.5% of sulfite in terms of weight and darkness ratio).
is preferable.

以上の要素をすべて含むこの発明の複合清缶剤は、低温
での速い脱酸素力と高い分散力を有し、ボイラーの腐食
とスケール付着を効果的に防止することができる。
The composite can cleaning agent of the present invention, which includes all of the above elements, has a fast deoxidizing power and a high dispersion power at low temperatures, and can effectively prevent boiler corrosion and scaling.

[発明の実施例] 触媒助剤としての硝酸カルシウムを含まない組成物Aと
、それを含む組成物Bについて脱酸素力を確認した。
[Example of the Invention] The oxygen scavenging ability of Composition A which does not contain calcium nitrate as a catalyst aid and Composition B which contains it was confirmed.

組成物   A(%)  組成物   B(%)KOH
4,5KOH4,5 に2  CO34,7K2  CO34,7KI  S
O328,3K2 803    28.3ソルビン酸
       ソルビン酸 カリウム  0.47     カリウム 0.47C
O8Oa    O,005C08OA    0.0
05ポリアクリル酸     ポリアクリル酸ナトリウ
ム4.7      ナトリウム4.7Ca(NO3)
    2 純水     57.325   純水     55
.325条件   水温 30℃ 水 :蒸留水 薬品投入量:300fItg/i この実施例の結果を図−2に示す。
Composition A (%) Composition B (%) KOH
4,5KOH4,5 to 2 CO34,7K2 CO34,7KIS
O328,3K2 803 28.3 Sorbic acid Potassium sorbate 0.47 Potassium 0.47C
O8Oa O,005C08OA 0.0
05 Polyacrylic acid Sodium polyacrylate 4.7 Sodium 4.7Ca (NO3)
2 Pure water 57.325 Pure water 55
.. 325 Conditions Water temperature: 30°C Water: Distilled water Chemical input amount: 300fItg/i The results of this example are shown in Figure 2.

これから明らかなように、上記の組成物としてカルシウ
ムが存在すると、溶存酸素の除去速度が大巾に向上する
As is clear from this, the presence of calcium in the above composition greatly increases the rate of removal of dissolved oxygen.

【図面の簡単な説明】[Brief explanation of the drawing]

図−1は、溶存酸素を測定するための装置の概略図、図
−2は、組成物Aと8とを投入した場合の時間と溶存酸
素濃度との関係を示したグラフである。 特許出願人   三浦工業株式会社 図−ユ 0         1        2     
   3(分)薬品投入からの時間
FIG. 1 is a schematic diagram of an apparatus for measuring dissolved oxygen, and FIG. 2 is a graph showing the relationship between time and dissolved oxygen concentration when compositions A and 8 were added. Patent applicant: Miura Kogyo Co., Ltd. 0 1 2
3 (minutes) Time from chemical injection

Claims (1)

【特許請求の範囲】 脱酸素剤として亜硫酸塩、その触媒としてコバルト塩、
スケール分散剤としてポリアクリル酸ナトリウム(分子
量1,000〜5,000)、ポリアクリル酸とコバル
トのキレート化を防止するための触媒助剤としてカルシ
ウムまたはマグネシウムの塩をそれぞれ含み、その各々
の割合が次の重量%であることを特徴とする水系複合清
缶剤。 亜硫酸塩15〜30 コバルト塩0.003〜0.01 ポリアクリル酸ナトリウム2〜5 カルシウム又はマグネシウム の硝酸塩2〜4
[Claims] Sulfite as an oxygen scavenger, cobalt salt as its catalyst,
Contains sodium polyacrylate (molecular weight 1,000-5,000) as a scale dispersant, calcium or magnesium salt as a catalyst aid to prevent chelation of polyacrylic acid and cobalt, and the proportions of each are A water-based composite can cleaning agent characterized by having the following weight percent: Sulfite 15-30 Cobalt salt 0.003-0.01 Sodium polyacrylate 2-5 Calcium or magnesium nitrate 2-4
JP31282186A 1986-12-27 1986-12-27 Aqueous composite antiscale agent for boiler Granted JPS63166981A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31282186A JPS63166981A (en) 1986-12-27 1986-12-27 Aqueous composite antiscale agent for boiler

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31282186A JPS63166981A (en) 1986-12-27 1986-12-27 Aqueous composite antiscale agent for boiler

Publications (2)

Publication Number Publication Date
JPS63166981A true JPS63166981A (en) 1988-07-11
JPH0141708B2 JPH0141708B2 (en) 1989-09-07

Family

ID=18033822

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31282186A Granted JPS63166981A (en) 1986-12-27 1986-12-27 Aqueous composite antiscale agent for boiler

Country Status (1)

Country Link
JP (1) JPS63166981A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012061461A (en) * 2010-08-20 2012-03-29 Tomita Pharmaceutical Co Ltd Scale generation inhibitor and scale generation inhibiting method
JP2012193434A (en) * 2011-03-17 2012-10-11 Kurita Water Ind Ltd Water treatment method of steam generation device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012061461A (en) * 2010-08-20 2012-03-29 Tomita Pharmaceutical Co Ltd Scale generation inhibitor and scale generation inhibiting method
JP2012193434A (en) * 2011-03-17 2012-10-11 Kurita Water Ind Ltd Water treatment method of steam generation device

Also Published As

Publication number Publication date
JPH0141708B2 (en) 1989-09-07

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