JPS5931498A - Condensate hydrogen oxygen concentration control equipment - Google Patents

Condensate hydrogen oxygen concentration control equipment

Info

Publication number
JPS5931498A
JPS5931498A JP57141841A JP14184182A JPS5931498A JP S5931498 A JPS5931498 A JP S5931498A JP 57141841 A JP57141841 A JP 57141841A JP 14184182 A JP14184182 A JP 14184182A JP S5931498 A JPS5931498 A JP S5931498A
Authority
JP
Japan
Prior art keywords
hydrogen
water
condensate
oxygen
equipment
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
JP57141841A
Other languages
Japanese (ja)
Other versions
JPH023960B2 (en
Inventor
道好 山本
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 JP57141841A priority Critical patent/JPS5931498A/en
Publication of JPS5931498A publication Critical patent/JPS5931498A/en
Publication of JPH023960B2 publication Critical patent/JPH023960B2/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)
  • Monitoring And Testing Of Nuclear Reactors (AREA)
  • Treatment Of Water By Oxidation Or Reduction (AREA)
  • Oxygen, Ozone, And Oxides In General (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は復水の通る配管機器の防食に利用される復水の
水素酸素#塵制御設備に関するもので、例えば沸)Jf
t水型原子力発電プラントの配管機器の防食のため特に
中性純水及び放射線環境下で復水の水紫酸累濃度を制御
して不働態化防食を図るに適する水素酸素濃度制御設備
に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to condensate hydrogen oxygen #dust control equipment used for corrosion prevention of piping equipment through which condensate passes, such as boiling water) Jf
The present invention relates to a hydrogen oxygen concentration control equipment suitable for controlling the cumulative concentration of water violet acid in condensate to achieve passivation corrosion protection, particularly in neutral pure water and radiation environments, for corrosion protection of piping equipment in T-water type nuclear power plants.

沸騰水型原子力発電プラントにおける配V機器の不働態
化防食のための中性純水環境下の復水の水素酸素#度制
御は、従来、第1図に例示したよ5に、原子炉圧力容器
1から出てタービン2を軸だ蒸気が復水器3で復水とな
った水′fi:ボング4によシ彷水飴化装置5に送シ、
ここで沖1ヒ屯れた往水が、tfンプ6から抜水管7を
通る際に、酸素ガスがンペ12から配管13により復水
系に酸素ガス全注入して抜水中の浴存酔糸を20〜20
01)pbOa度に制御して、下流の機器である低圧給
水加熱器8.給水ン」ポンプ9および市)E絹水加〃5
器10や配;、g 11 qυの防食を行うものであシ
、これにより原子炉圧力容器1内への不糊物の持込みを
防ぎ、ノラントの放射能を低減することに成功している
Conventionally, hydrogen/oxygen degree control of condensate in a neutral pure water environment for passivation and corrosion protection of V distribution equipment in a boiling water nuclear power plant has been carried out based on the reactor pressure as shown in Figure 1. The steam coming out of the container 1 and passing through the turbine 2 becomes condensed water in the condenser 3;
When the incoming water that has been pumped offshore passes through the drain pipe 7 from the TF pump 6, all the oxygen gas is injected into the condensate system from the pump 12 through the pipe 13, and the water remains in the bath during draining. 20~20
01) Low-pressure feed water heater, which is downstream equipment, controlled to pbOa degrees8. Water supply pump 9 and city) E silk water addition 5
This prevents corrosion of the vessel 10, the parts, and g 11 qυ, thereby successfully preventing the introduction of waste materials into the reactor pressure vessel 1 and reducing the radioactivity of Nolant.

ところで、近年、ノリ子炉容器内の放射線下における水
の放射細分解による生成物として過酸化水素f■202
や酸素02が生じそのIW イP’Mか心安以上に多く
なるので、これらの溶存景を低減する防食方法の検Nを
侠するようになった。例えば原子炉起動前に片子炉圧力
芥器1内を真空脱気する方法が採用されている。しかじ
加害運転中は、この真空脱気はタノノ釆がないので、炉
内Cニー矩の浴仔飲系や過岐化水計の」l全確度になっ
ている。そのレベルは酩・素で200 ppb程度であ
るか、原子炉−次冷却系のオーステナイトステンレス銅
にとっては、この?l■史に低下させる方が、応力腐食
割れ等の腐食埃象を更に緩和するのに有効であることが
知見された。そのだめの方法として、第2図に示すよう
な水素を注入する水系1ン累決1隻制御方法が考えられ
ている。これはljM壁21を有する電解容器20の阻
極、陽極22.23に向流電蝕24から@流を流し、電
が≠容器20中の水の電気分解で発生した水素と酸素を
取出し、水素をガスの状態でv25及びノズル26から
原子炉−冷却系のり水管7に注入する方法である。27
は上流側のゆ水の1部を1に解答器20に流入させると
ともに酸素をガスの状態で一部後水管7に注入する配管
、28は余剰酸素の排出管である。
By the way, in recent years, hydrogen peroxide f■202 has been produced as a product of the radioactive decomposition of water under radiation in the Nori reactor vessel.
Since IW and oxygen 02 are generated and the amount of IW IP'M is more than safe, we have begun to investigate corrosion prevention methods to reduce these dissolved phenomena. For example, a method is adopted in which the inside of the single reactor pressure tank 1 is vacuum degassed before starting up the nuclear reactor. During the damage operation, this vacuum degassing is not effective, so the accuracy of the bathtub drinking system and water meter in the C knee rectangle inside the furnace is at full accuracy. The level is about 200 ppb in terms of alcohol/element, or is it this for the austenitic stainless steel copper in the sub-cooling system of the nuclear reactor? It has been found that lowering the corrosion resistance to a temperature of 1.1 is more effective in further alleviating corrosion dust phenomena such as stress corrosion cracking. As a solution to this problem, a water-based one-ship one-ship control method in which hydrogen is injected, as shown in FIG. 2, has been considered. This is done by passing @ current from the countercurrent electrolytic etch 24 to the blocking poles and anodes 22 and 23 of the electrolytic vessel 20 having ljM walls 21, and the current ≠ taking out hydrogen and oxygen generated by electrolysis of water in the vessel 20. This is a method in which hydrogen is injected in a gaseous state from the v25 and the nozzle 26 into the reactor cooling system water pipe 7. 27
28 is a pipe for allowing a part of the upstream water to flow into the analyzer 20 and partially injecting oxygen in the form of a gas into the rear water pipe 7; 28 is a pipe for discharging excess oxygen.

第2図に示しfCC氷水水素酸索請ル制御方法は、酸素
ガスを列−ンベから注入するという第1図の従来方法に
比べて、ボンベの交換を再々hう必要がないという運転
上の利点はあるが、水素をガス状態で注入するため、そ
の注入する水系の8釈が不安定・不良となシ、注入点よ
り下流にあるポンプ゛のキャビテーションや熱交換器内
での停滑全佑するという欠点がある。
Compared to the conventional method shown in Fig. 1, which involves injecting oxygen gas from a train tank, the fCC ice water, hydrogen, and oxygen line control method shown in Fig. 2 has operational advantages such as eliminating the need to repeatedly exchange cylinders. Although there are advantages, since hydrogen is injected in a gaseous state, the injection of water into the water system may be unstable or defective, and cavitation of the pump downstream of the injection point or stalls in the heat exchanger may occur. It has the disadvantage of being dull.

本発明の目的(−」、上記従来技術の欠点に鑑み、安定
した水素及び酸素を復水系に注入して注水後の希釈を良
好にすると共にその濃度奮確実に制御し4むる抜水の水
$醗索一度制御設備を提供するにある。
Purpose of the present invention (-) In view of the above-mentioned drawbacks of the prior art, stable hydrogen and oxygen are injected into the condensate system to improve dilution after water injection and to reliably control the concentration of the water that is drained. Once you explore $, we will provide you with control equipment.

本発明の水素酸素濃度制御1]設備は、水を171it
At、電びF、で′11を気分解する′K]、解答器と
、該電解容器に往水・糸から復水の1g1)を畳入する
流路と、該電解容器中でその陰極汲ひ陽極近傍に夫々発
生した水素及び酸素を互に混らないよ5Kして水溶液状
態で後水系に注入する各別の注入用151i、路と、上
記の注入を受けた後水系中の復水の水差濃度及び酸系濃
度を夫々検出する水素計及び酸素計と、これら検出され
た水;4.−W′番度及び酸素濃度に従って上記各別の
注入路における水素水溶液及び1g≠水浴准の夫々の流
おを制御する制御装置とからなることを特徴としている
Hydrogen oxygen concentration control of the present invention 1] The equipment has 171 liters of water.
gaseous decomposition of '11 with At, electric power F, 'K]; Separate injection channels 151i and 151i for pumping and injecting the hydrogen and oxygen generated near the anode into the aqueous system after heating them to 5K so as not to mix them with each other and injecting them into the aqueous system after receiving the above injection; 4. A hydrogen meter and an oxygen meter that detect the difference concentration and acid concentration of water, respectively, and the detected water; 4. - A control device for controlling the flow of the hydrogen aqueous solution and 1 g≠water bath in each of the above-mentioned separate injection channels according to the W' number and the oxygen concentration.

以下、本発明の火軸例を第3図によシ統明する。Hereinafter, an example of the fire axis of the present invention will be explained with reference to FIG.

この図において第2図に示した従来技術におりる部分と
対応する部分は同じ符号を付しである。後水管7を流れ
る往水の一部は弁43.デンプ42゜弁44を含む管路
27を通って[N容器2oに給水される。電解容器2o
の中では直流電諒24よシ給電される陰4iI!、22
及び陽極23の近傍に夫々水素及び酸素が水の電気分解
の結果発生する。陽極及び陽極間の隔壁21はこれら水
素と酸素を互に混らないように分離する。発生した水素
は、水に溶存した状態即ち水溶液の状態で、調整弁33
を含む配管25を経て後水管7に注入される。また上記
の発生した酸素は弁39を含む配管29を経て同じく水
に一溶存した水溶液の状態で往水管7に注入される。こ
のように注入された水素及び酸素は、復水管7の上記注
入点よシ下流fll11に設けられた水素計35及び酸
素計41で注入後の往水中の夫々の濃度が検出され、こ
の検出濃度に応じた電気信号が調整装置34及び4oに
送られ、これによル弁33及び39をii#J 整して
夫々配〜・25及び29を通る水素水溶液及び酸素水浴
液の流量を制御する。このようにして原子炉への給水禾
での水の水素及びvV累濃度を一層に保つ。
In this figure, parts corresponding to those in the prior art shown in FIG. 2 are given the same reference numerals. A portion of the outgoing water flowing through the rear water pipe 7 is supplied to the valve 43. Water is supplied to the [N container 2o] through a conduit 27 containing a starch 42° valve 44. Electrolytic container 2o
Inside, the shade 4iI is powered by the DC power supply 24! , 22
Hydrogen and oxygen are generated near the anode 23 as a result of water electrolysis. The anodes and the partition wall 21 between the anodes separate hydrogen and oxygen so that they do not mix with each other. The generated hydrogen is in a state dissolved in water, that is, in an aqueous solution state, when the hydrogen is passed through the regulating valve 33.
The water is injected into the rear water pipe 7 through the pipe 25 containing the water. The generated oxygen is also injected into the outgoing water pipe 7 through the pipe 29 including the valve 39 in the form of an aqueous solution dissolved in water. The concentrations of the hydrogen and oxygen injected in this manner in the incoming water after injection are detected by a hydrogen meter 35 and an oxygen meter 41 provided downstream of the injection point in the condensate pipe 7, and the detected concentration Electric signals corresponding to the 25 and 29 are sent to the regulators 34 and 4o, which adjust the valves 33 and 39 to control the flow rates of the hydrogen aqueous solution and the oxygen aqueous solution passing through the valves 25 and 29, respectively. . In this way, the cumulative hydrogen and vV concentration of the water in the water supply to the reactor is better maintained.

−力、諭剰な水素、酸素が′d1解谷器20中に生成し
ないように+r−i流′I+J、源24の軍がLを71
.!I側1すべくル1′!I整装置34.40をセ、ト
シておく。更に、電解容器20中に余剰に発生した水素
及び酸基のガスは夫々気液分離ヘッダ30.36及び配
置I31 +37を経て水素貯A′λ装置15°32お
よびfM來貯蔵装置38に貯蔵される。この貯蔵ガスは
発電ハ[内の他の適宜の用途に用いることができる。
- force, to prevent excessive hydrogen and oxygen from being generated in the ``d1 disintegration device 20 +r-i flow ``I+J, the army of source 24 has L 71
.. ! I side 1 to 1'! I Set the adjustment device 34.40 aside. Further, hydrogen and acid radical gas generated in excess in the electrolytic vessel 20 are stored in the hydrogen storage A'λ device 15° 32 and the fM storage device 38 via the gas-liquid separation header 30, 36 and the arrangement I31 +37, respectively. Ru. This stored gas can be used for other suitable uses within the power generation system.

第4図にボす他の火砲例は第3図に小した実施例と似て
いるが、異る点は、例えば電気分解が停%などで停止し
たとき貯蔵装M32,38に貯蔵されていた水素及び酸
基をバックアップ用として〜水管7に注入するだめの配
’1!750 、51及び升52.53を備えているこ
とである。弁52゜53は両整装置行34.40により
調整もれる。
The other firearm example shown in FIG. 4 is similar to the example shown in FIG. It is equipped with a tank 1.750, 51 and a square 52.53 for injecting hydrogen and acid groups into the water pipe 7 as backup. Valves 52 and 53 are regulated by both adjustment device lines 34 and 40.

以上説明したように不発ゆ」によれば、水の電気分解を
用いて安定した水素及び版木を発生させ、月つこれを夫
々水溶液の状態で復水中に注入するので、その注入によ
る希釈が良好で且つその訣度′fb11俳が俸実となる
利点がある。史に水の’ltf、 m分h・Iで生じた
水素及び酸素を貯蔵して訃き、必要に応じ、バックアッ
プの7こめこれを少水示に注入す7Lば、イリ水の水素
し素函度制御11のイ3ね性を一層向上させることがで
きる。
As explained above, according to ``Fudyu'', stable hydrogen and woodblocks are generated using water electrolysis, and each of these is injected into condensate in the form of an aqueous solution, so dilution by injection is possible. It has the advantage that it is good and its strength is good. If you store the hydrogen and oxygen generated in the water 'ltf, m min h・I in the history, and if necessary, inject this into the low water display as a backup 7L, the hydrogen and nitrogen in the water The robustness control 11 can be further improved.

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

ゐす1[ηt;J従米の沸騰水型)1只子力発′r在ン
°ラントにおけるイシ水の水メーr狭累i11度のfl
ill仰手段の例を小す模式図、第2図は4水の水素酸
累痰1B: 1li1.l rol1手段の他の従来例
を示す概略図、第3図は本発明の1実施例を示す系統図
、第4図kl、不発りjの他の実施例を示す系統図であ
る。 1・・・原子炉      2・・・タービン3・・ゆ
水器      4・・・ンj?ンノ5・・・復水浄化
装置   7・・・俵水管8・・・低圧給水加熱器  
9・・・給水ボンダ10・・・高圧給水加熱器 11・
・・配管12・・・酸系ガスン1.!ンペ 20−・・
箪解谷器21・・・隔壁      22・・・陰極2
3・・・陽極      24・・・!116t+:電
源25・・・水メ・5注入管   27・・・復水?j
p出管29・・・酸素Y1人肯   32・・・水系貯
威装首34・・・水素刊・η整装置  35・・・水素
剖゛38 ・・・ ri:2 L包針 ノ151: 装
置      40 ・・・d 素11ノ=jl:i 
二(;j1□1f丘41・・・酸素計。 第1図 第:2メ1 第3図
1 [ηt; boiling water type of boiling water]
FIG. 2 is a schematic diagram showing an example of an ill elevating means. 3 is a schematic diagram showing another conventional example of the rol1 means, FIG. 3 is a system diagram showing one embodiment of the present invention, and FIG. 4 is a system diagram showing another embodiment of kl and misfire j. 1... Nuclear reactor 2... Turbine 3... Water heater 4... Nj? 5...Condensate purification device 7...Bale water pipe 8...Low pressure feed water heater
9... Water supply bonder 10... High pressure water supply heater 11.
...Piping 12...Acid gas 1. ! Empe 20-...
Kankatani device 21... partition wall 22... cathode 2
3...Anode 24...! 116t+: Power supply 25...Water meter/5 injection pipe 27...Condensate? j
P outlet pipe 29...Oxygen Y1 person confirmation 32...Water system storage equipment 34...Hydrogen publication/η adjustment device 35...Hydrogen analysis 38...ri:2 L packaging needle No. 151: Device 40...d element 11 no=jl:i
2(;j1□1f hill 41...Oxygen meter. Figure 1: 2me 1 Figure 3

Claims (1)

【特許請求の範囲】 1、 直流?iJ: Mj、にょシ水を電気分解する電
解容器と、該’iIi解答器に復水系から復水の1部を
導入するηれ路と、該電解容器内でその陽極及び陽極の
近傍に夫々発生した水素及び酸系を互に混らないように
して水浴像状態で復水系に注入する各別の注入用?Ir
、路と、上記の注入を受けた細氷系中の復水の水素濃り
頭及び酸素濃度を夫々検出する水ヌミ肘及び酸素削と、
これら検出された水素濃度及び酸素濃度に従って上B[
1各別の注入路における水−素水浴港及び酸素水溶液の
流h;を制御する開側1装置とからなることを特徴とす
る復水の水素酸累旋吸制御設備。 2 上Njシ酸巣酎耐検出した瞑度に従って電解容器へ
の面幅電流を調節して水の電気分解虻を調′察すること
を特徴とする特許81jオの範囲第1項記載の復水の水
素酸累繰度71;II御設備。 3、 電解容器中に発生した余剰の水素゛及び酸素をガ
ス状で夫々貯蔵する貯蔵装置を備えたことを%徴とする
%#f請求の範囲第1項記載の復水の敞累水素酸度匍」
御設備。 4、貯蔵装置に貯蔵された水系及び酸素を、心安に応じ
後水系に注入する管路及び該管路中の弁を備えたことを
特徴とする特¥[Mh求の範囲第3項記載の復水の水素
酸素閾度制側1設備。
[Claims] 1. Direct current? iJ: Mj, an electrolytic vessel for electrolyzing water, an η channel for introducing a part of condensate from the condensate system into the 'iIi answerer, and an anode and an anode near the anode in the electrolytic vessel, respectively. Is it for separate injections in which the generated hydrogen and acid systems are injected into the condensate system in a water bath state so that they do not mix with each other? Ir
, a water shaving element and an oxygen shaving element for detecting the hydrogen enrichment head and oxygen concentration of the condensate in the injected thin ice system, respectively;
According to these detected hydrogen and oxygen concentrations, upper B[
1. Hydrogen acid accumulation control equipment for condensate, comprising a water-hydrogen water bath port in each separate injection path and an open side device for controlling the flow h of an oxygen aqueous solution. 2. The condensate described in Paragraph 1 of the scope of Patent No. 81J, which is characterized in that the electrolytic decomposition of water is monitored by adjusting the surface width current to the electrolytic vessel according to the detected degree of condensation. Hydrogen acid repeatability 71; II equipment. 3. The cumulative hydrogen acidity of the condensate according to claim 1, which is characterized by the fact that it is equipped with a storage device for storing surplus hydrogen and oxygen generated in the electrolytic vessel in gaseous form, respectively. crawl"
Your equipment. 4. A feature characterized by comprising a pipe line and a valve in the pipe line for injecting the water system and oxygen stored in the storage device into the water system as needed [Mh requirement range as described in item 3] Condensate hydrogen oxygen threshold system side 1 equipment.
JP57141841A 1982-08-16 1982-08-16 Condensate hydrogen oxygen concentration control equipment Granted JPS5931498A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57141841A JPS5931498A (en) 1982-08-16 1982-08-16 Condensate hydrogen oxygen concentration control equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57141841A JPS5931498A (en) 1982-08-16 1982-08-16 Condensate hydrogen oxygen concentration control equipment

Publications (2)

Publication Number Publication Date
JPS5931498A true JPS5931498A (en) 1984-02-20
JPH023960B2 JPH023960B2 (en) 1990-01-25

Family

ID=15301393

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57141841A Granted JPS5931498A (en) 1982-08-16 1982-08-16 Condensate hydrogen oxygen concentration control equipment

Country Status (1)

Country Link
JP (1) JPS5931498A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005224696A (en) * 2004-02-12 2005-08-25 Hoshizaki Electric Co Ltd Rust preventive functional water, method and system for manufacturing rust preventive functional water

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005224696A (en) * 2004-02-12 2005-08-25 Hoshizaki Electric Co Ltd Rust preventive functional water, method and system for manufacturing rust preventive functional water

Also Published As

Publication number Publication date
JPH023960B2 (en) 1990-01-25

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