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JPH0335385B2 - - Google Patents
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JPH0335385B2 - - Google Patents

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Publication number
JPH0335385B2
JPH0335385B2 JP61251759A JP25175986A JPH0335385B2 JP H0335385 B2 JPH0335385 B2 JP H0335385B2 JP 61251759 A JP61251759 A JP 61251759A JP 25175986 A JP25175986 A JP 25175986A JP H0335385 B2 JPH0335385 B2 JP H0335385B2
Authority
JP
Japan
Prior art keywords
water
corrosion
pure water
dissolved oxygen
specific conductivity
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
JP61251759A
Other languages
Japanese (ja)
Other versions
JPS6296898A (en
Inventor
Taku Honda
Akira Minato
Masakyo Izumitani
Eiji Kashimura
Katsumi Oosumi
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP61251759A priority Critical patent/JPS6296898A/en
Publication of JPS6296898A publication Critical patent/JPS6296898A/en
Publication of JPH0335385B2 publication Critical patent/JPH0335385B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin

Landscapes

  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Description

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

本発明は酸素を溶存する純水と金属材料とが接
する系における金属材料を防食する新規な発電プ
ラントに関する。 酸素を溶存する純水と金属材料とが接する発電
プラントにおいては金属材料が腐食され、純水が
静止している場合の腐食の程度は溶存酸素濃度が
高くなるほど著しく、特に、水が酸素を濃度約40
ないし約30000ppb溶存する場合に金属材料に腐
食が起りその防食対策が要望される。 特に、BWR(沸騰水型原子炉)発電プラント
では定期検査等による運転停止時において復水、
給水系配管が大気開放状態で5ないし8ppmもの
高い溶存酸素濃度の水にさらされ、配管の金属材
料、とりわけ、炭素鋼が著しく腐食される。そし
て、腐食に伴い生じた腐食生成物(鉄酸化物を主
体としたものでクラツドと呼ばれる。)は、プラ
ント起動時に原子炉内に持込まれて燃料棒に付着
し熱効率を低下し、又燃料棒を破損するおそれが
ある。さらに、燃料棒に付着したクラツドは放射
化された後剥離して炉再循環系配管等に再付着し
て配管等の表面線量率を増大させ、定期検査等の
従事者の対し放射能被爆量の増大を招く危険もあ
る。これらの理由から、BWR発電プラントの運
転停止時における復水、給水系配管の防食対策は
重要な課題となつている。 従来、酸素を溶存する純水と金属材料とが接す
る系、特に、BWR発電プラントの運転停止時に
おける配管の防食にはホツトドレンオフと呼ばれ
る水抜き乾燥法が一部のプラントについて採用さ
れてきた。この方法は、プラント運転停止時に給
水が冷却しきらないうちに水抜きし余熱で配管表
面を乾燥するものであるが、プラントの構造上の
差異によりすべてのプラントに適用できるもので
はなく、又、水抜きに伴い生ずる多量の放射性廃
液の処理にも問題がある。さらに、この水抜き乾
燥法は操作も煩雑なので、運転停止が短期の場合
には適当でない。 また、特開昭52−85696号公報には、原子炉の
起動前に復水器の真空度を調節して溶存酸素濃度
を50〜200ppbに保つことにより給復水系配管の
腐食を防止する方法が開示されている。しかし、
溶存酸素濃度の制御だけでは前述の配管を十分に
防食することはできない。 他の防食方法として火力発電プラントにおい
て、運転停止が短期間の場合にヒドラジン添加に
よる満水保管法が採用され、運転停止が長期間の
場合には水抜き後窒素ガスを封入する乾燥保管法
が採用されているが、BWRプラントにおいては
添加したヒドラジンは後の起動時までに除去しな
ければならず、窒素ガスも脱気しなければならな
い等、後処理に問題があるので、これらの方法を
BWR発電プラントの防食に適用することはでき
ない。 本発明の目的は発電プラントのタービン停止時
に酸素を溶存する純水と復水器及び給水系の金属
材料とが接する系における金属材料を防食する発
電プラントを提供することである。 本発明のより具体的な目的はBWR発電プラン
トのタービン停止時における復水、給水系配管の
腐食を防止する発電プラントを提供することであ
る。 本発明は、水蒸気によつて回転する蒸気タービ
ン、前記水蒸気を純水に戻す復水器、前記純水の
中の塩類を除去する脱塩器、前記純水を加熱し再
び水蒸気にする加熱源に前記純水を供給する給水
系を有する発電プラントにおいて、前記給水系と
復水器とを連結する再循環配管を設けて該配管、
復水器、脱塩器及び給水系の前記純水の閉じた循
環経路を構成し、該経路内で前記純水の比電導度
を0.5μS/cm以下に保つ幻記脱塩器を有すること
を特徴とする発電プラントにある。特に加熱源と
して原子炉、火力が用いられる。 本発明における系では純水は酸素を溶存してい
るが、純水の溶存酸素濃度は金属材料が酸素溶存
の純水に接して腐食を発生させ防食が問題となる
範囲のものであり、金属材料の種類によつても異
なるが、具体的には約40ないし約30000ppbであ
る。前記のように、BWRプラントの運転停止時
における復水、給水系配管は大気開放状態で5な
いし8ppmの溶存酸素濃度の水に接することにな
るので、この配管の金属材料を防食するのに本発
明は特に好適である。 本発明において防食の対象となる金属材料とし
ては、酸素が溶存する水、特に、溶存酸素濃度約
40ないし約30000ppbの水に接して防食が問題と
なる特に例えば、炭素鋼、低合金鋼、ステンレス
鋼、銅及びその合金が挙げられる。BWR発電プ
ラントの復水、給水系配管の材料である炭素鋼は
本発明により有効に防食される。 本発明においては純水の比電導度を0.5μS/cm
以下に保つことが要件の一つであり、そのように
調整する手段は例えば、粒状陽・陰両イオン交換
樹脂を充填した脱塩器に純水を通導されて比電導
度を低下させることにより達成することができ
る。本発明において純水の比電導度を0.5μS/cm
以下に保つと金属材料の腐食速度が著しく減少
し、有効な防食が達成でき、特に、0.1μS/cm以
下に保つと防食効果は一層顕著になる。しかし、
純水の比電導度が0.5μS/cmを越えると有効な防
食効果を期待することができない。 本発明における他の要件の一つは純水を流動さ
せるポンプを有することであり、純水を流動させ
るとは、純水が金属材料の表面で静止状態になら
ないようにすることを意味する。純水の流動の程
度は、比電導度を特定値に保つことと相まつて本
発明の目的が達成されるものであればよく、流速
0.2ないし1cm/S程度又はそれ以上が普通であ
る。純水を流動させるには、例えば、低圧ポンプ
を用いて水を動かすだけでよい。純水を流動させ
ることは比電導度を0.5μS/cm以下に保つのに役
立つのみならず純水中の溶存酸素濃度の局部的相
異によつて生ずる局部電池の発生(これが腐食の
原因となる)を防止する。また、一般に純水と接
する金属表面には純水中の溶存酸素との反応によ
つて極く薄い酸化皮膜が発成され、この酸化皮膜
は下働態化作用によつて腐食の進行を防げる。し
かしこの酸化皮膜は極く微細なクラツクを有して
おり、このクラツクを介して腐食が進行する危険
があるが、純水を流動させることはこのクラツク
を通して、溶存酸素を金属に供給してその部分に
酸化皮膜を生成させてクラツク部分での腐食の進
行を防止するものと考えられる。 本発明を実施する温度は普通30ないし40℃であ
り、時間は実施の態様に応じ適宜決めることがで
きる。 実施例 1 水の比電導度を脱塩器により低下させ、異なる
比電導度における防食効果を調べた。 溶存酸素濃度8ppmの水に第1表に示す炭素鋼
を浸漬し、流速0.2cm/S、温度30℃において腐
食速度を測定した。
The present invention relates to a novel power generation plant that prevents corrosion of metal materials in a system where pure water containing dissolved oxygen comes into contact with the metal materials. In power generation plants where pure water containing dissolved oxygen comes into contact with metallic materials, the metallic materials are corroded, and when the pure water is still, the degree of corrosion becomes more pronounced as the dissolved oxygen concentration increases. about 40
Corrosion occurs in metal materials when dissolved in amounts of 30,000 ppb to 30,000 ppb, and corrosion prevention measures are required. In particular, in BWR (boiling water reactor) power plants, condensate and
Water supply piping is exposed to water with a dissolved oxygen concentration as high as 5 to 8 ppm when exposed to the atmosphere, and the metal materials of the piping, especially carbon steel, are severely corroded. Corrosion products (commonly composed of iron oxides and called crud) generated as a result of corrosion are brought into the reactor at the time of plant startup and adhere to the fuel rods, reducing thermal efficiency. There is a risk of damaging it. Furthermore, after being activated, the crud attached to the fuel rods peels off and re-attaches to the reactor recirculation system piping, etc., increasing the surface dose rate of the piping, etc. There is also the risk of causing an increase in For these reasons, corrosion prevention measures for condensate and water supply system piping during shutdown of BWR power plants have become an important issue. Conventionally, a water draining and drying method called hot drain-off has been used in some plants to prevent corrosion of piping in systems where pure water containing dissolved oxygen and metal materials come into contact, especially when BWR power plants are shut down. . This method involves draining water before the supply water is completely cooled when plant operation is stopped, and drying the piping surface using residual heat. However, it cannot be applied to all plants due to differences in plant structure. There are also problems with the disposal of the large amount of radioactive waste fluid that is generated as a result of draining water. Furthermore, this draining and drying method is complicated to operate, so it is not suitable for short-term shutdowns. Additionally, Japanese Patent Application Laid-Open No. 52-85696 describes a method for preventing corrosion of water supply and condensate system piping by adjusting the degree of vacuum in the condenser and maintaining the dissolved oxygen concentration at 50 to 200 ppb before starting the reactor. is disclosed. but,
Controlling the dissolved oxygen concentration alone cannot sufficiently protect the piping described above from corrosion. As other corrosion prevention methods, in thermal power plants, when the operation is stopped for a short period of time, a full water storage method with the addition of hydrazine is adopted, and when the operation is stopped for a long period of time, a dry storage method is adopted where water is drained and then nitrogen gas is filled. However, in a BWR plant, the added hydrazine must be removed before startup, and the nitrogen gas must also be degassed, so these methods are not recommended.
It cannot be applied to corrosion protection in BWR power plants. An object of the present invention is to provide a power generation plant that prevents corrosion of metal materials in a system where pure water containing dissolved oxygen comes into contact with metal materials of a condenser and water supply system when the turbine of the power generation plant is stopped. A more specific object of the present invention is to provide a power generation plant that prevents corrosion of condensate and water supply system piping when the turbine of a BWR power generation plant is stopped. The present invention relates to a steam turbine rotated by steam, a condenser that returns the steam to pure water, a desalination device that removes salts from the pure water, and a heating source that heats the pure water and turns it into steam again. In a power generation plant having a water supply system that supplies the pure water to a water supply system, a recirculation piping is provided that connects the water supply system and a condenser, and the piping,
Constructing a closed circulation path for the pure water in the condenser, demineralizer, and water supply system, and having a phantom demineralizer that maintains the specific conductivity of the pure water at 0.5 μS/cm or less within the path. Located in a power generation plant featuring: In particular, nuclear reactors and thermal power are used as heating sources. In the system of the present invention, pure water has dissolved oxygen, but the dissolved oxygen concentration in pure water is within a range where metal materials come into contact with pure water containing dissolved oxygen and cause corrosion, causing problems in corrosion protection. Although it varies depending on the type of material, the specific amount is about 40 to about 30,000 ppb. As mentioned above, when a BWR plant is shut down, the condensate and water supply piping is exposed to the atmosphere and comes into contact with water with a dissolved oxygen concentration of 5 to 8 ppm, so it is important to prevent corrosion of the metal materials of these piping. The invention is particularly suitable. In the present invention, the metal material targeted for corrosion protection is water containing dissolved oxygen, especially water with a dissolved oxygen concentration of about
Particular examples where corrosion protection becomes a problem in contact with water of 40 to about 30,000 ppb include carbon steel, low alloy steel, stainless steel, copper and its alloys. The present invention effectively prevents corrosion of carbon steel, which is the material for condensate and water supply piping in BWR power plants. In the present invention, the specific conductivity of pure water is 0.5μS/cm.
One of the requirements is to maintain the specific conductivity below, and the means for adjusting it in this way is, for example, passing pure water through a demineralizer filled with granular positive and negative ion exchange resin to lower the specific conductivity. This can be achieved by In the present invention, the specific conductivity of pure water is 0.5μS/cm.
If it is kept below, the corrosion rate of metal materials will be significantly reduced and effective corrosion protection can be achieved.In particular, if it is kept below 0.1μS/cm, the corrosion protection effect will be even more remarkable. but,
If the specific conductivity of pure water exceeds 0.5 μS/cm, no effective anticorrosion effect can be expected. One of the other requirements of the present invention is to have a pump that flows pure water, and flowing pure water means that the pure water does not remain stationary on the surface of the metal material. The degree of flow of pure water may be such that the purpose of the present invention is achieved together with maintaining the specific conductivity at a specific value, and the flow rate
The normal value is about 0.2 to 1 cm/S or more. To flow pure water, it is sufficient to move the water using, for example, a low-pressure pump. Flowing pure water not only helps keep the specific conductivity below 0.5 μS/cm, but also helps prevent the formation of local batteries caused by local differences in dissolved oxygen concentration in pure water, which can cause corrosion. prevention). In addition, a very thin oxide film is generally formed on metal surfaces that come into contact with pure water by reaction with dissolved oxygen in the pure water, and this oxide film prevents corrosion from progressing due to its lowering effect. However, this oxide film has extremely fine cracks, and there is a risk that corrosion will progress through these cracks, but flowing pure water supplies dissolved oxygen to the metal through these cracks. It is thought that this prevents corrosion from progressing in the cracked area by forming an oxide film on the cracked area. The temperature at which the present invention is carried out is usually 30 to 40°C, and the time can be determined as appropriate depending on the mode of implementation. Example 1 The specific conductivity of water was lowered using a demineralizer, and the anticorrosion effect at different specific conductivities was investigated. The carbon steel shown in Table 1 was immersed in water with a dissolved oxygen concentration of 8 ppm, and the corrosion rate was measured at a flow rate of 0.2 cm/S and a temperature of 30°C.

【表】 第1図は炭素鋼の腐食速度と水の比電導度との
関係を示し、比電導度が0.5μS/cmより小さい純
水では腐食速度が著しく減少する。比電導度
0.1μS/cmの純水による腐食速度は約1mg/d
m2/月であり、この場合炭素鋼は外観上金属光沢
を呈し、孔食の発生は全く認められず、防食効果
は顕著であつた。 実施例 2 水の流速と腐食速度との関係を種々の比電導度
において調べた。 即ち、温度が30℃、溶存酸素濃度が8ppmであ
り、比電導度が夫々2.12μS/cm、1.07μS/cm、
0.53μS/cm及び0.12μS/cmの水に炭素鋼(第1
表)を浸漬し、種々の流速における炭素鋼の腐食
速度を求めた。 結果は、第2図に示す通りであり、水の比電導
度が約1μS/cm以上では水の流速が大きくなるの
に伴つて腐食速度も増大するのが、水の比電導度
が約0.5μs/cm以下では水の流速が大きくなるの
に伴なつて腐食速度は減少する傾向が認められ
る。 実施例 3 溶存酸素濃度5ppmの水に炭素鋼(第1表)を
浸漬し、水の比電導度0.1μS/cm、流速1cm/S、
温度35℃において腐食減量の経時変化を測定し
た。結果は第3図(水の流動と腐食減量との関係
を示す)に示すとおりであり、流動水中では曲線
Aの如く時間経過にかかわりなく殆んど一定して
腐食減量が小さく抑えられていたが、流動を一旦
停止して静止状態にすると曲線Bの如く約70時間
後に腐食減量は約50mg/dm2に達し腐食が進行し
た。しかし、再び水を流動させると腐食減量はそ
のまま一定を保ち、それ以上腐食は進行しなかつ
た。 参考のために、前記と同じ実験を静止水中で行
なつたところ、曲線Cの如く時間経過とともに腐
食減量は増加した。 以上、腐食減量の点からみて純水を流動させる
ことが本発明による防食に必須であるこがわかる
が、このことは腐食速度の点からしても明らかで
あり、腐食速度は流動水中で約1mg/dm2/月、
静止水中で約300mg/dm2/月であつた。 実施例 4 異なる溶存酸素濃度における炭素鋼(第1表)
の防食効果を調べた。 比電導度0.1μS/cmを有する高純度の水中にお
いて炭素鋼を浸漬し、流速1cm/S、温度35℃に
おいて腐食速度を測定した。結果は第4図(腐食
速度と溶存酸素濃度との関係を示す)に示すとお
りであり、腐食速度は、実線Aの如く溶存酸素濃
度40ppb以上で急に減少し、大気開放状態に相当
する5ないし8ppmの溶存酸素濃度では腐食速度
は約1mg/dm2/月であつた。これによれば、溶
存酸素濃度40ppb以上において防食効果が発揮さ
れることがわかる。 なお、静止水中では腐食速度は点線Bの如く溶
存酸素濃度が大きくなるにつれて増加し、5ない
し8ppmで約300mg/dm2/月に達した。この結果
を前記の流動水中におけるそれと対比すると、純
水を流動させることが防食に必須であることがわ
かる。 実施例 5 異なる比電導度における炭素鋼(第1表)の腐
食ないし防食の効果を調べた。 純水の比電導度を0.2ないし0.5μS/cmに保ち、
溶存酸素濃度40ppb、流速1cm/S、温度35℃、
浸漬時間3960時間の条件下において、浸漬後の炭
素鋼表面を走査電子顕微鏡により観察した。その
結果金属表面は結晶粒径1μm程度のマグネタイ
トを主とする結晶によりμmオーダの厚さにおお
われていることが確認された。 純水の比電導度を0.1μs/cm以下に保ち、前記
と同じ条件下において、浸漬後の炭素鋼表面を同
様に観察した。その結果結晶粒径は0.2μm程度で
あり、金属表面はきわめて密なÅオーダの薄膜層
でおおわれていることが確認された。 以上の結果からすると、純水の比電導度を0.2
ないし0.5μs/cm、特に0.1μs/cm以下に保つた場
合にすぐれた腐食抑制効果、すなわち、防食効果
を得られることがわかる。なお、防食効果を腐食
減量でみると、比電導度0.2ないし0.5μs/cmの場
合517mg/dm2であり、0.1μs/cmの場合33.2mg/
dm2であり、これによれば、比電導度を低く保つ
た方が一層顕著な防食効果を発揮することがわか
る。 実施例 6 第5図はBWR発電プラントの系統概略図であ
り、1は原子炉、2はタービン、3は復水器、4
は復水脱塩器、5は復水低圧ポンプ、6は給水再
循環ラインである。 第5図に示すBWR発電プラントのタービン運
転停止時から起動までの間において本発明の防食
方法を実施した。BWR発電プラントの復水、給
水系配管は主に炭素鋼製であり、これと接する水
は大気開放状態で溶存酸素濃度5ないし8ppmを
示した。給水再循環ライン6による循環系を用い
て復水脱塩器4に水を通導し、比電導度測定器を
用いて水の比電導度を測定するとともに0.5μs/
cm以下に保つように流速1cm/Sで循環流動させ
た。750時間後において復水、給水系配管には全
く腐食は認められなかつた。 尚、本実施例において、復水器3の主な構成要
素は鋼合金製の冷却管及び炭素鋼製の復水器容器
であり、その接水面積は夫々約40000m2及び8000
m2である。また、復水低圧ポンプ5から復水脱塩
器4を通り、給水再循環ライン6を経て復水器3
に至る系統には給水加熱器及び配管があり、給水
加熱器の加熱管はステンレス鋼製、給水加熱器の
胴体は低合金鋼製、配管は炭素鋼製であり、これ
らの接水面積は夫々約15000m2、約100m2及び1500
m2である。本実施例を実施した時、復水脱塩器4
の入口及び出口で水中の鉄、銅、クロム及びニツ
ケル濃度を測定したところ、両測定点においてこ
れらの金属濃度は常に1ppb以下であつた。 以上の説明から明らかなように、本発明は簡便
な手段によつて純水と接する金属材料を防食する
ものであり、特に、BWR発電プラントのタービ
ン運転停止時における復水、給水系配管の防食に
好適であり、実用価値も高く工業的にきわめて有
意義なものである。
[Table] Figure 1 shows the relationship between the corrosion rate of carbon steel and the specific conductivity of water. The corrosion rate is significantly reduced in pure water with a specific conductivity of less than 0.5μS/cm. specific conductivity
Corrosion rate with pure water of 0.1μS/cm is approximately 1mg/d
m 2 /month, and in this case, the carbon steel had a metallic luster in appearance, no pitting corrosion was observed, and the anticorrosion effect was remarkable. Example 2 The relationship between water flow rate and corrosion rate was investigated at various specific conductivities. That is, the temperature is 30°C, the dissolved oxygen concentration is 8 ppm, and the specific conductivity is 2.12 μS/cm and 1.07 μS/cm, respectively.
Carbon steel (first
Table) was immersed to determine the corrosion rate of carbon steel at various flow rates. The results are shown in Figure 2. When the specific conductivity of water is about 1 μS/cm or more, the corrosion rate increases as the water flow rate increases, but when the specific conductivity of water is about 0.5 Below μs/cm, the corrosion rate tends to decrease as the water flow rate increases. Example 3 Carbon steel (Table 1) was immersed in water with a dissolved oxygen concentration of 5 ppm, the specific conductivity of the water was 0.1 μS/cm, the flow rate was 1 cm/S,
Changes in corrosion weight loss over time were measured at a temperature of 35°C. The results are shown in Figure 3 (showing the relationship between water flow and corrosion weight loss), and in flowing water, the corrosion weight loss was kept small and almost constant regardless of the passage of time, as shown by curve A. However, when the flow was once stopped and the state was brought to a standstill, the corrosion weight loss reached approximately 50 mg/dm 2 after approximately 70 hours as shown by curve B, and corrosion progressed. However, when water was allowed to flow again, the corrosion loss remained constant and corrosion did not progress any further. For reference, the same experiment as above was conducted in still water, and as shown by curve C, the corrosion weight loss increased with time. From the above, it can be seen that flowing pure water is essential for corrosion prevention according to the present invention from the perspective of corrosion weight loss, but this is also clear from the perspective of corrosion rate, which is approximately 1 mg in flowing water. /dm 2 /month,
The concentration in still water was approximately 300 mg/dm 2 /month. Example 4 Carbon steel at different dissolved oxygen concentrations (Table 1)
The anticorrosive effect of Carbon steel was immersed in high-purity water with a specific conductivity of 0.1 μS/cm, and the corrosion rate was measured at a flow rate of 1 cm/S and a temperature of 35°C. The results are shown in Figure 4 (showing the relationship between corrosion rate and dissolved oxygen concentration), and the corrosion rate suddenly decreases when the dissolved oxygen concentration exceeds 40 ppb, as shown by solid line A, which corresponds to the open atmosphere condition. At dissolved oxygen concentrations of 8 to 8 ppm, the corrosion rate was approximately 1 mg/dm 2 /month. According to this, it can be seen that the anticorrosion effect is exhibited at dissolved oxygen concentrations of 40 ppb or higher. In addition, in still water, the corrosion rate increased as the dissolved oxygen concentration increased, as shown by dotted line B, and reached about 300 mg/dm 2 /month at 5 to 8 ppm. Comparing this result with that in flowing water, it can be seen that flowing pure water is essential for corrosion prevention. Example 5 The corrosion or anticorrosion effect of carbon steel (Table 1) at different specific conductivities was investigated. Keep the specific conductivity of pure water at 0.2 to 0.5μS/cm,
Dissolved oxygen concentration 40ppb, flow rate 1cm/S, temperature 35℃,
The carbon steel surface after immersion was observed using a scanning electron microscope under the condition of immersion time of 3960 hours. As a result, it was confirmed that the metal surface was covered with a thickness on the order of μm by crystals mainly composed of magnetite with a grain size of about 1 μm. The carbon steel surface after immersion was similarly observed under the same conditions as above, with the specific conductivity of pure water being kept at 0.1 μs/cm or less. As a result, it was confirmed that the crystal grain size was approximately 0.2 μm, and the metal surface was covered with an extremely dense thin film layer on the order of Å. Based on the above results, the specific conductivity of pure water is 0.2
It can be seen that an excellent corrosion inhibiting effect, that is, an anticorrosive effect can be obtained when the corrosion rate is maintained at 0.5 to 0.5 μs/cm, particularly 0.1 μs/cm or less. In addition, when looking at the corrosion protection effect in terms of corrosion loss, it is 517mg/dm2 when the specific conductivity is 0.2 to 0.5μs/cm, and 33.2mg/ dm2 when the specific conductivity is 0.1μs/cm.
dm 2 , and it can be seen from this that a more significant corrosion prevention effect is exhibited by keeping the specific conductivity low. Example 6 Figure 5 is a schematic system diagram of a BWR power plant, where 1 is a nuclear reactor, 2 is a turbine, 3 is a condenser, and 4 is a system diagram of a BWR power plant.
5 is a condensate demineralizer, 5 is a condensate low pressure pump, and 6 is a feed water recirculation line. The corrosion prevention method of the present invention was carried out from the time the turbine operation of the BWR power plant shown in FIG. 5 was stopped to the time it was started. The condensate and water supply system piping of the BWR power plant is mainly made of carbon steel, and the water in contact with it showed a dissolved oxygen concentration of 5 to 8 ppm when exposed to the atmosphere. Water is passed through the condensate demineralizer 4 using a circulation system with a water supply recirculation line 6, and the specific conductivity of the water is measured using a specific conductivity measuring device, and the specific conductivity of the water is measured at 0.5 μs/
Circulation was carried out at a flow rate of 1 cm/s to maintain the flow rate at 1 cm/s or less. After 750 hours, no corrosion was observed in the condensate and water supply piping. In this embodiment, the main components of the condenser 3 are a cooling pipe made of steel alloy and a condenser container made of carbon steel, and their contact areas are approximately 40,000 m 2 and 8,000 m 2 , respectively.
m2 . In addition, the water flows from the condensate low pressure pump 5 through the condensate demineralizer 4 and through the feed water recirculation line 6 to the condenser 3.
The system leading to the system includes a feed water heater and piping.The heating tube of the feed water heater is made of stainless steel, the body of the feed water heater is made of low alloy steel, and the piping is made of carbon steel.The water contact area of each of these is Approx. 15000m 2 , Approx. 100m 2 and 1500
m2 . When this embodiment is implemented, the condensate demineralizer 4
When we measured the concentrations of iron, copper, chromium, and nickel in the water at the inlet and outlet, the concentrations of these metals were always below 1 ppb at both measurement points. As is clear from the above description, the present invention provides corrosion protection for metal materials that come into contact with pure water by simple means, and is particularly applicable to corrosion protection of condensate and water supply system piping when the turbine of a BWR power plant is stopped. It is suitable for this purpose, has high practical value, and is of great industrial significance.

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

第1図は比電導度と腐食速度との関係図、第2
図は水の流速と腐食速度との関係図、第3図は時
間と腐食減量との関係図、第4図は溶存酸素濃度
と腐食速度との関係図、第5図はBWR発電プラ
ント系統概略図である。 1……原子炉、2……タービン、3……復水
器、4……復水脱塩器、5……復水低圧ポンプ、
6……給水再循環ライン。
Figure 1 is a diagram of the relationship between specific conductivity and corrosion rate, Figure 2
Figure is a diagram of the relationship between water flow rate and corrosion rate, Figure 3 is a diagram of the relationship between time and corrosion loss, Figure 4 is a diagram of the relationship between dissolved oxygen concentration and corrosion rate, and Figure 5 is a schematic diagram of the BWR power plant system. It is a diagram. 1... Nuclear reactor, 2... Turbine, 3... Condenser, 4... Condensate demineralizer, 5... Condensate low pressure pump,
6... Water supply recirculation line.

Claims (1)

【特許請求の範囲】 1 蒸気タービン、復水器、脱塩器及び水蒸気を
形成する加熱源に純水を供給する給水系を有する
発電プラントにおいて、前記給水系と復水器とを
連結する再循環配管が設けられ、前記純水が前記
給水系より前記配管、復水器、脱塩器及び給水系
を順次循環する閉じた経路を構成し、該経路内で
前記純水を循環させるポンプを有し、かつ前記純
水の比電導度を0.5μS/cm以下に保つ前記脱塩器
を有することを特徴とする発電プラント。 2 前記加熱源は源子炉である特許請求の範囲第
1項記載の発電プラント。
[Scope of Claims] 1. In a power generation plant having a water supply system that supplies pure water to a steam turbine, a condenser, a demineralizer, and a heating source that forms steam, a regeneration system that connects the water supply system and the condenser is provided. Circulation piping is provided, forming a closed path in which the pure water sequentially circulates from the water supply system through the piping, the condenser, the demineralizer, and the water supply system, and a pump that circulates the pure water within the path. and the demineralizer that maintains the specific conductivity of the pure water at 0.5 μS/cm or less. 2. The power generation plant according to claim 1, wherein the heating source is a source furnace.
JP61251759A 1986-10-24 1986-10-24 power plant Granted JPS6296898A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61251759A JPS6296898A (en) 1986-10-24 1986-10-24 power plant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61251759A JPS6296898A (en) 1986-10-24 1986-10-24 power plant

Publications (2)

Publication Number Publication Date
JPS6296898A JPS6296898A (en) 1987-05-06
JPH0335385B2 true JPH0335385B2 (en) 1991-05-28

Family

ID=17227501

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61251759A Granted JPS6296898A (en) 1986-10-24 1986-10-24 power plant

Country Status (1)

Country Link
JP (1) JPS6296898A (en)

Also Published As

Publication number Publication date
JPS6296898A (en) 1987-05-06

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