JPS58208700A - Method and device for processing radioactive liquid waste - Google Patents

Method and device for processing radioactive liquid waste

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Publication number
JPS58208700A
JPS58208700A JP9252782A JP9252782A JPS58208700A JP S58208700 A JPS58208700 A JP S58208700A JP 9252782 A JP9252782 A JP 9252782A JP 9252782 A JP9252782 A JP 9252782A JP S58208700 A JPS58208700 A JP S58208700A
Authority
JP
Japan
Prior art keywords
waste liquid
radioactive
organic solvent
treating
radioactive waste
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.)
Pending
Application number
JP9252782A
Other languages
Japanese (ja)
Inventor
大東 祥晃
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.)
Toshiba Corp
Nippon Genshiryoku Jigyo KK
Nippon Atomic Industry Group Co Ltd
Original Assignee
Nippon Genshiryoku Jigyo KK
Tokyo Shibaura Electric Co Ltd
Nippon Atomic Industry Group 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 Nippon Genshiryoku Jigyo KK, Tokyo Shibaura Electric Co Ltd, Nippon Atomic Industry Group Co Ltd filed Critical Nippon Genshiryoku Jigyo KK
Priority to JP9252782A priority Critical patent/JPS58208700A/en
Publication of JPS58208700A publication Critical patent/JPS58208700A/en
Pending legal-status Critical Current

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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】 [発明の技術分野〕 本発明は放射性廃液の処理方法および装置に関するもの
であり、特に原子カプラント等における配管等金属表面
に付着した放射性物質を電解液と接触さ°せることによ
り、溶解除去する除染作業の結t!発生する放射性除染
廃液の処理方法および装置に関覆るものである。
[Detailed Description of the Invention] [Technical Field of the Invention] The present invention relates to a method and apparatus for treating radioactive waste liquid, and in particular to a method and apparatus for treating radioactive waste liquid, in particular a method for bringing radioactive substances attached to metal surfaces such as piping in an atomic couplant into contact with an electrolytic solution. As a result, the decontamination work that involves dissolving and removing the material will end! It concerns methods and equipment for processing radioactive decontamination waste fluid generated.

[発明の技術的背II] 原子力発電プラント等の原子力施設の配管全屈表面に付
着した放射性物質を電解液と接触させて溶解除去でる除
染作業の結東qじるtlA射性物性物質んだ電解廃液の
処理は、一般にこの電解廃液を中和し・τから濃縮11
゛濃縮し、水と1縮廃液に分離して濃縮廃液をセメント
あるいはアスファルトで固化することにより処理されて
いた。上記の電解廃液の中和を、例えばカセイソーダを
用いて(うな−)k@合、次の反応式 %式% により、Na25O+が発生プる。
[Technical Background of the Invention II] Radioactive materials used in decontamination work to dissolve and remove radioactive materials attached to the fully curved surface of piping in nuclear facilities such as nuclear power plants by contacting them with an electrolyte. Generally, the electrolytic waste liquid is treated by neutralizing it and concentrating it from τ11.
``It was treated by concentrating it, separating it into water and a condensed waste liquid, and solidifying the concentrated waste liquid with cement or asphalt. When the above electrolytic waste liquid is neutralized using, for example, caustic soda, Na25O+ is generated according to the following reaction formula.

中和処理後反応生成物を通常蒸発濃縮器で濃縮して、回
収または環境放出すべき凝縮水と廃液の主要部分を含む
IIIKB廃液とに分1111するが、このとさ中和処
理により発生したNa 2804は濃縮廃液側に含まれ
る。他にこの分野で1縮のために用いられる他の方法と
しては、逆浸透膜法、電気透析法があるがいずれの方法
の場合でも、濃縮廃液側にはNa25O*が含まれる。
After the neutralization process, the reaction product is usually concentrated using an evaporative concentrator to separate the condensed water to be recovered or released into the environment and the IIIKB waste liquid containing the main part of the waste liquid. Na 2804 is contained in the concentrated waste liquid side. Other methods used for condensation in this field include reverse osmosis membrane method and electrodialysis method, but in either method, the concentrated waste liquid side contains Na25O*.

しかして、原子hプラント等にお【プる配管等の金属表
面に付着した放IjJ性物質を電解液と接触させて溶解
除去でる除染作業から発生する除染廃液は、hII制能
レベルが比較的商い状態にあることが多く、この廃液を
通常の中和濃縮設備で処即しノζ場合には、放射能レベ
ル上昇に伴う作業員の被曝の危険が1じる1゜ 1発明の目的] 本発明は]配した従来の欠点を解消すべくなされたもの
で、改良された放射性廃液処理技術を提供することにあ
り、特に中和1m縮操作法にお(プるよ記危険を除去線
たは軽減させた処理方法および装置を提供づることにあ
る。
Therefore, decontamination waste liquid generated from decontamination work in which IJJ-emitting substances adhering to metal surfaces such as piping connected to an atomic h plant, etc. is dissolved and removed by contacting with an electrolyte, has a hII control level. In many cases, the waste liquid is in a relatively commercial condition, and if this waste liquid is treated with normal neutralization and concentration equipment, there is a high risk of exposure of workers due to increased radioactivity levels. [Purpose] The present invention has been made in order to eliminate the drawbacks of the conventional technology, and its purpose is to provide an improved radioactive waste liquid treatment technology, and particularly to reduce the risk of neutralization by 1 m. It is an object of the present invention to provide a processing method and apparatus for reducing removal lines.

[発明の概要] 本発明の放射性廃液の処理方法は、原子カプラント等に
おりる金属表面に付着した放射性物質を電解液と接触さ
せて溶解除去する除染作業等の結泉発生した放@竹物質
を含む電W?液廃液を、水不溶性または水難溶性キレー
ト化合物を形成するキレート化剤を加えることC=−よ
り処1!し・、間開にまたは次に有機溶媒と混合して上
記処理により住じIC放射性キレニド化合物を電解廃液
から有a溶媒中に抽出し、次に放射性キレ−1・化合物
の除かれlζ電解廃液を水とlll縮廃液とに分離りる
一方、11機溶媒と放射性キレート・化合物とを9鑵す
ることにより、作!!員に対する危険を除去した処理方
法および装置を提供しようとするものである。
[Summary of the Invention] The method for treating radioactive waste liquid of the present invention is a method for treating radioactive waste liquid that is produced by condensation during decontamination work, etc., in which radioactive substances attached to the metal surface of an atomic couplant, etc. are brought into contact with an electrolytic solution and removed by dissolution. Electricity W containing matter? Adding a chelating agent that forms a water-insoluble or slightly water-soluble chelate compound to the liquid waste liquid from C=-1! Then, the IC radioactive compound is extracted from the electrolytic waste solution into a solvent by the above treatment by intermittent or then mixed with an organic solvent, and then the radioactive compound is removed from the electrolytic waste solution. By separating 11 solvents and radioactive chelate/compound into 9 pieces while separating it into water and lll condensate liquid, it is made! ! The purpose of the present invention is to provide a treatment method and device that eliminates danger to personnel.

放射性除染廃液を濃縮Aるための上記した従来の中和濃
縮法においては、実務上連続した一員作業を極端に続け
ることは比較的少なく、かつ放則能レベルの^いl縮廃
液は、イの都度バッチ処理されるため被曝の危#竹はi
!’6いが、本発明の処理方法および装置によれば、こ
れに特定のキレート他剤処理および溶媒抽出を組合せる
ことによって連続的に、かつ被曝のおそれなく処理操作
を行なうことかできる 本発明にお(プるル−ト化剤としては、EDTA等のポ
リアミノカルボン酸類、クエン酸等のオー塾ジカルボン
酸類および縮合リン酸塩を除くすべてのキレート化剤を
用いることができる。特にジメチルグリフIイシム、オ
キシン、ジチゾン、ト諷すフルオ[]アセチルア廿トン
(Ce H5,02SF3 )[1’ A△」およびキ
レート樹脂、例えばクロルメチル化したスチレンとジビ
ニルベンゼンとの共重合体を処即しT Cf−1p’N
 (CH2C00H) /Wを導入した樹脂、3−オキ
シフ1ニルチオ尿素、(NH’2 C3NHC6H40
H−3) と71/−ルとの縮合体樹脂、没食子酸とレ
ゾルシン、ホルムアルデヒドの共縮合により生成した樹
脂は良好な結果をもたらす。EDTA等のポリアミノカ
ルボン酸、クエン酸等のAキシカルボン酸類および縮合
リン酸塩は放射性廃液と水溶性キレート化合物を1成す
るので好ましくない。トリフルオロアセデルアセ1〜ン
は特に良好な結果をもたらす。
In the above-mentioned conventional neutralization and concentration method for concentrating radioactive decontamination waste liquid, it is relatively rare for one person to continue continuous work in practice, and the decondensed liquid at the unrestricted level is Bamboo is at risk of radiation exposure because it is processed in batches each time.
! However, according to the treatment method and apparatus of the present invention, by combining the treatment with a specific chelating agent and solvent extraction, the treatment operation can be carried out continuously and without fear of exposure to radiation. As the rooting agent, all chelating agents except polyaminocarboxylic acids such as EDTA, dicarboxylic acids such as citric acid, and condensed phosphates can be used. In particular, dimethylglyph I Ishim, oxine, dithizone, fluoro[]acetylatone (Ce H5,02SF3) [1' A△] and chelate resins, such as copolymers of chloromethylated styrene and divinylbenzene, are treated with T Cf. -1p'N
(CH2C00H) /W-introduced resin, 3-oxyphinylthiourea, (NH'2 C3NHC6H40
Condensate resins of H-3) and 71/-l, resins produced by co-condensation of gallic acid, resorcinol, and formaldehyde give good results. Polyaminocarboxylic acids such as EDTA, A-oxycarboxylic acids such as citric acid, and condensed phosphates are not preferred because they form a water-soluble chelate compound with the radioactive waste liquid. Trifluoroacetyl acetate gives particularly good results.

本発明における溶媒としては、水に実質的に溶解しない
、すべての有機溶媒を用いることができる。特に低沸点
の有機溶媒が好ましく、そのうち特にトリクロロトリフ
ルオロ−トタン、ジクロロジフルオロエタンのような低
沸点ハロゲン化炭化水素溶媒が適当である。
As the solvent in the present invention, any organic solvent that does not substantially dissolve in water can be used. Particularly preferred are organic solvents with a low boiling point, and among them, low-boiling halogenated hydrocarbon solvents such as trichlorotrifluorototane and dichlorodifluoroethane are particularly suitable.

[発明の実施例1 以下本発明の一実施例を図面を参照して訂細(ご説明す
る。
[Embodiment 1 of the Invention An embodiment of the present invention will be explained in detail below with reference to the drawings.

図面は本発明の放射性物質除去の98埋り法おJ。The drawing shows the 98 method of removing radioactive substances according to the present invention.

び装置の・−例を示す概略図である。1 is a schematic diagram illustrating an example of an apparatus.

図面に示で放射性廃液の98311+装置は、放剛性電
解廃液貯4!i1と、キレート化剤を溶解させた有機溶
媒の添加装置(以上添加装置という)2と、1゛・液(
溶媒相)導出管3aと電解廃液の軽液(水性相)導出管
31)とを接続した放射性物質のキレート化合物形成槽
並溶媒抽出槽(以下抽出槽という)3と、軽液導出管3
1)の他端に配置した受は槽4を介して接続された蒸発
濃縮装置5と、φ液導出管3aの他端に接続された蒸留
装置6とから構成されている。、抽出槽3は敢剛性電解
廃液貯槽1、添加装置2と配管1a、3cおよび2aに
より接続されており、配管3Cの先端は抽出槽3の底部
に挿入され、イの先端はラッパ状に拡開され端面(J多
孔ノズル3(1が固設されている。7はポンプである。
The radioactive waste liquid 98311+ equipment shown in the drawing is a rigid electrolytic waste liquid storage 4! i1, an addition device for the organic solvent in which the chelating agent is dissolved (hereinafter referred to as the addition device) 2, and 1゛・liquid (
A radioactive substance chelate compound formation tank and solvent extraction tank (hereinafter referred to as extraction tank) 3, which connects a solvent phase) lead-out pipe 3a and a light liquid (aqueous phase) lead-out pipe 31) of electrolytic waste liquid, and a light liquid lead-out pipe 3
1) The receiver disposed at the other end is composed of an evaporation concentration device 5 connected via a tank 4 and a distillation device 6 connected to the other end of the φ liquid outlet pipe 3a. , the extraction tank 3 is connected to the rigid electrolytic waste liquid storage tank 1 and the addition device 2 by pipes 1a, 3c, and 2a, the tip of the pipe 3C is inserted into the bottom of the extraction tank 3, and the tip of the pipe 3C is expanded into a trumpet shape. The open end face (J multi-hole nozzle 3 (1) is fixedly installed. 7 is a pump.

蒸発IIl縮馳買5は、加熱化5a、蒸発缶5bおよび
凝縮器5Cとからなっており、上部配管5dどポンプ8
を有する十部配管5eとにより循環路が形成され又いる
。加熱化5aはポンプ9を有する配管5′:lfにより
受り槽4と接続され−ている。この配管5fからは配管
5qが分岐し、この配管59の末端は図示を省略した受
・け槽に開口している。
The evaporator IIl condenser 5 consists of a heating unit 5a, an evaporator 5b, and a condenser 5C, and includes an upper pipe 5d and a pump 8.
A circulation path is formed by the ten-piece pipe 5e. The heating tank 5a is connected to the receiving tank 4 by a pipe 5':lf with a pump 9. A pipe 5q branches off from the pipe 5f, and the end of the pipe 59 opens into a receiving tank (not shown).

10.11は開閉バルブである。凝縮器5Cは蒸発缶5
bの上部と配管5hにより接続されここで生じた凝縮水
は配管5i=によりサンプルタンク12に排出される。
10.11 is an on-off valve. Condenser 5C is evaporator 5
It is connected to the upper part of the pipe 5h by a pipe 5h, and the condensed water generated here is discharged to the sample tank 12 by a pipe 5i=.

蒸留装置6は、ヒータ13を備えた蒸留器6aとこの蒸
留器6aの頂部に配管6bにより接続さ−れた凝・幅器
6Cとから構成されている。凝縮器6Cr:凝縮された
有機溶媒は配管6dから図示を省略した回収槽へ送られ
る一方、生したスラッジは配管6eから排出される。1
4.15は開閉バルブである。
The distillation apparatus 6 is composed of a distiller 6a equipped with a heater 13 and a condenser/sparder 6C connected to the top of the distiller 6a by a pipe 6b. Condenser 6Cr: The condensed organic solvent is sent from piping 6d to a collection tank (not shown), while the raw sludge is discharged from piping 6e. 1
4.15 is an on-off valve.

この装置においては、−例として放射性廃液貯槽1中に
は、原fカプラント等における配管など金属表面にイ1
椙した放@性物質を電解液と接触させることにより溶解
除去づる除染作業のv5果発住でる電解質を含んだ放射
性廃液16が貯えられる1゜放射性廃液貯槽1に貯えら
れた放射性廃液16はポンプ7ににり配管1a、3cを
抽出槽3に)ン(られ、多孔ノズル3dにより抽出槽3
の底部から上りへ向かつて噴出される。一方添加装諮2
内の=ルー−1〜化剤を溶解した有機溶媒17(ま配管
2aを介して抽出槽3の上部から注入され、抽出槽33
内C放耐性廃液と図、示を省略した攪拌装Wにより混合
される。これらの混液内で放射性物質はキレ−・1・他
剤と及応して水に不溶性またはI溶性の4レ一ト化合物
を形成し、このキレート化合物は4機溶媒中に溶解する
。キレート化合物が有機溶媒中に溶解した後混液を静置
して[!とψ液とに分離さゼた後、重液は蒸溜装置0に
磨かれ、そこで蒸溜おれる。有機溶媒として(−リクロ
ルトリフルオロ]タンを用いた場合にはその沸点は低く
、1気圧で47.6℃にすぎず、蒸溜により容易にスラ
ッジと溶媒蒸気とに分れ、スラッジは配管6eを軽て装
置外に排出され、蒸気分は凝縮器6C内で凝縮された後
、配管6dから排出され、再使用される。 方、軽液は
軽液導出管3bを経て、受は槽/l c=貯溜される。
In this device, for example, in the radioactive waste liquid storage tank 1, there are
The radioactive waste liquid 16 stored in the radioactive waste liquid storage tank 1 is stored at The pump 7 connects the pipes 1a and 3c to the extraction tank 3, and the porous nozzle 3d connects the pipes 1a and 3c to the extraction tank 3.
It is ejected from the bottom upwards. On the other hand, additive
The organic solvent 17 in which the chemical agent is dissolved is injected from the upper part of the extraction tank 3 through the pipe 2a, and
It is mixed with the internal C release resistant waste liquid using a stirring device W (not shown). In these mixed solutions, the radioactive substance reacts with the chelate, 1, and other agents to form a water-insoluble or 1-soluble chelate compound, and this chelate compound is dissolved in the chelate solvent. After the chelate compound is dissolved in the organic solvent, the mixture is allowed to stand and [! After being separated into ψ liquid and ψ liquid, the heavy liquid is polished to distillation unit 0, where it is distilled. When (-lichlorotrifluoro)thane is used as the organic solvent, its boiling point is low, only 47.6°C at 1 atm, and it easily separates into sludge and solvent vapor by distillation, and the sludge flows through pipe 6e. The vapor is condensed in the condenser 6C and then discharged from the pipe 6d to be reused.On the other hand, the light liquid passes through the light liquid outlet pipe 3b, and the light liquid is transferred to the tank/tank. l c = stored.

受は槽4中の1液はポンプ9により蒸発濃縮装置5に送
られ蒸発濃縮されてサンプルタンク12中に放出される
。、なお受【プ槽4の段階において軽油の状態が再使用
または環境放出可能であるときは軽液は配管5gを経て
回収もしくは環境放出される。トリクロルト・リフルオ
ロエタン溶媒は、密度が1 、565!] /′cイ(
25℃)と比較的大ぎいので水性相との比重差分離が比
較的速やかに行なわれるうえに沸点も低いため水と比べ
て低温度で蒸溜生成ができ、省エネルギーの観点からも
侵ねたものということができる。また、キレート化剤と
して使用するTTA(1−リフルオルアセチルアゼトン
)は、その沸点が103〜107℃であり1例えば溶媒
であるトリクロルトリフルオロエタン相を50℃で蒸溜
しても、溶媒側に残留して繰返し再使用で・きるという
利点がある。
The liquid in the receiving tank 4 is sent to the evaporative concentrator 5 by the pump 9, where it is evaporated and concentrated and discharged into the sample tank 12. If the state of the light oil in the receiving tank 4 is such that it can be reused or released into the environment, the light liquid is recovered or released into the environment through the pipe 5g. Trichlorotrifluoroethane solvent has a density of 1,565! ] /'c i(
Since it is relatively large (25°C), separation from the aqueous phase due to the difference in specific gravity occurs relatively quickly, and its boiling point is low, so it can be distilled and produced at a lower temperature than water, making it unbeatable from an energy-saving perspective. It can be said that. In addition, TTA (1-lifluoroacetyl azetone) used as a chelating agent has a boiling point of 103 to 107°C, and even if the trichlorotrifluoroethane phase, which is a solvent, is distilled at 50°C, the solvent side remains It has the advantage that it remains in the water and can be reused repeatedly.

この実施例においては、キレ−1〜化剤の1]−Δは比
較的低いρF1−で充分に放射竹物穎と4レ一1〜化合
物を形成するので、電解性汚染廃液をあらかじめl) 
H調節でる必要性は比較的小さい。なお、この実施例に
お(ブる蒸発濃縮器は濃縮器の 例にすぎず、蒸発器部
分を3! ’a M E:L K置、電気りi装置と覆
ることもむろん可能ぐある。
In this example, the electrolytic contaminated waste liquid was prepared in advance to form a compound with the radiation bamboo glume at a relatively low ρF1-Δ of the cleaning agent.
The need for H adjustment is relatively small. Note that the evaporative concentrator described in this embodiment is only an example of a concentrator, and it is of course possible to replace the evaporator section with an electric device.

(発明の効宋コ 以上の説明からも明らかなように、本発明によれば除染
廃液中(7)M射性不純物(!111co、60co)
等を選択的に除去覆ることができ、故銅慴物買除去後の
処理は#制能レヘルが低減されてるので、簡単な廃棄物
処理装置で処理か可能になり、成用性汚染物の濃縮、同
化ちり能となり、その産朦土の効果は若しい。
(Effects of the invention) As is clear from the above explanation, according to the present invention, (7) M-emitting impurities (!111co, 60co) in decontamination waste liquid
etc. can be selectively removed and covered, and since the control level is reduced in the treatment after the removal of dead copper, it is possible to treat it with a simple waste treatment equipment, and it is possible to eliminate synthetic contaminants. It becomes concentrated and assimilated dust, and the effect of its production is young.

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

図面は本発明のtll@性廃液の処理方法および装置の
 実施例を概要的に示り構成図である。 1・・・・・・・・・・・・放射性電解廃液貯槽2・・
・・・・・・・・・・イi機溶媒の添加装置ご3・・・
・・・・・・・・・4レ一1〜化合物形成槽と溶媒抽出
槽 J a・・・・・・・・壬液導出管 3b・・・・・・・・・軽液導出管 4・・・・・・・・・・・・受番プ槽 5・・・・・・・・・・・蒸発濃縮装置F) a・・・
・・・・・・加熱色 5tl・・・・・・・・・蒸発缶 5C・・・・・・・・・凝縮器 6・・・・・・・・・・・・蒸留装置 6a・・・・・・・・・蒸留器 6G・・・・・・・・・凝縮器 16・・・・・・・・・放射性廃液 ]7・・・・・・・・・有機溶媒
The drawings are schematic diagrams showing an embodiment of the tll@ waste liquid treatment method and apparatus of the present invention. 1... Radioactive electrolyte waste liquid storage tank 2...
・・・・・・・・・Ai solvent addition device 3...
......4 layers 1 to compound formation tank and solvent extraction tank J a...Liquid outlet pipe 3b...Light liquid outlet pipe 4・・・・・・・・・・・・Receiving tank 5・・・・・・・・・Evaporation concentrator F) a...
...Heating color 5tl... Evaporator 5C... Condenser 6... Distillation device 6a...・・・・・・・・・Distiller 6G・・・・・・・・・Condenser 16・・・・・・Radioactive waste liquid] 7・・・・・・・・・Organic solvent

Claims (1)

【特許請求の範囲】 (1)原子カプラント等において発生慢る脱塩装置の再
生廃液を始めとする各種廃液あるいは金属表面に(1着
した放射性物質を電解液と接触させて溶解除去づる除染
作業薄の結果発生した放射性物質を含む電解廃液を、該
放射性物質と水不溶性まt、 ’4.L水輔溶牲↓レー
1へ化合物を形成するキレ−1へ他剤を加えることによ
り処理し、同時にまたは次に有機溶媒と混合して前記処
理により住した放射JIT4.−uレー1〜化合物を電
解廃液から前記有機溶媒中に抽出し、次に放射性キレー
ト化合物の除かれた電解廃液を水とiff縮廃液とに分
1llIスる一方、前記有機溶媒と放射性キレ−;−化
合物とを分=m+することを特徴と覆る放射性廃液の処
理lj法。 (2)pH調節剤または中和剤をキレート化合物を形成
力る際および/′または電解廃液の濃縮の際加えること
を特徴とする特許請求の範囲第1項記載の放射性廃液の
処理方法。 (3)有機溶媒として、低沸点で、かつ水との比重の差
の大きい有機溶媒を用いる特許請求の範囲第1項記載の
放射fi廃液の処理り法。 (4)有Pi溶媒として、ハロゲン化炭化水素を用いる
特許請求の範囲第3項記載の放射性廃液の処理方法。 (5)有機溶媒として、トリクロルトリフルオロエタン
を用いる特許請求の範囲第4項記載の放射性廃液の処即
プJ汰。 (6)放射性電解廃液の′a縮が、蒸発濃縮により行な
われることを特徴とする特許請求の範囲第1項記載の放
射性廃液の処理方法。 (7)放射性電解廃液の濃縮が、逆浸透膜または電気透
析にJ、り行なわれることを9、シ徴とでる格許請求の
範囲第1項記載の放射性廃液の処理力法。 (8)放射性キレート化合物を含む溶液を蒸溜して放射
性蒸溜残査と未及応4レート化剤を含む回収溶媒とに分
離し、回収溶媒をさらに抽出に再使用することを特徴と
する特許請求の範囲第1項記 。 載の放射性廃液の処理方法。 (9ン放割性電解廃液訂槽と斗レート化剤および有機溶
媒添加装置とを導入管により接続した放射性物質のキレ
ート化含物形成槽兼溶媒抽出横に、■−下に離間させて
水性相導圧管と有機溶媒相導出管どのそれぞれ・・端を
接続し、前記水性層導出管の他端は電解ml液のlft
装置を接続し、前記溶媒抽出槽の他端は蒸留精製装置へ
接続したことを特徴とする放射性廃液の処理装置。 (10)横縮装宵が加熱缶を付設した蒸発濃縮槽である
特許請求の範囲第9項記載の放射性廃液の処理装置。 (11)歯輪装置が逆浸透圧濃縮装置である特許請求の
範囲第9項記載の放射性廃液の処理装置。 (12)濃縮装蔚が電気透析濃縮装置である特許請求の
範囲第9項記載の放射性廃液の処理装置。
[Scope of Claims] (1) Decontamination by dissolving and removing radioactive substances on various waste liquids, including recycled waste liquid from desalination equipment, which is frequently generated in nuclear couplants, etc., or on metal surfaces. The electrolytic waste solution containing radioactive substances generated as a result of the work is treated by adding other agents to the radioactive substances and water-insoluble materials, which form a compound into the water-soluble ↓ray-1. and simultaneously or subsequently mixed with an organic solvent to extract the radioactive JIT 4.-u-ray 1 ~ compounds that have been absorbed by the treatment from the electrolytic waste solution into the organic solvent, and then the electrolytic waste solution from which radioactive chelate compounds have been removed. A method for treating radioactive waste liquid characterized by adding 1 l l l to water and IF degenerate waste liquid, while adding 1 l l l to the organic solvent and the radioactive chemical compound for 1 ll l l. The method for treating radioactive waste liquid according to claim 1, characterized in that the agent is added when forming a chelate compound and/or when concentrating the electrolytic waste liquid. (3) As the organic solvent, a low boiling point , and a method for treating radioactive fi waste liquid according to claim 1, which uses an organic solvent having a large difference in specific gravity from water. (4) Claim 1, which uses a halogenated hydrocarbon as the Pi-containing solvent. The method for treating radioactive waste liquid according to claim 3. (5) The method for treating radioactive waste liquid according to claim 4, using trichlorotrifluoroethane as the organic solvent. (6) The method for treating radioactive waste liquid according to claim 4. The method for treating a radioactive waste liquid according to claim 1, characterized in that the concentration is carried out by evaporative concentration. (7) The radioactive electrolyte waste liquid is concentrated by a reverse osmosis membrane or electrodialysis. 9. A method for treating radioactive waste liquid according to claim 1, which is a symptom of this. (8) A solution containing a radioactive chelate compound is distilled to produce a radioactive distillation residue and an unaccompanied 4-rating agent. A method for treating radioactive waste liquid according to claim 1, characterized in that the radioactive waste liquid is separated into a recovered solvent containing Next to the radioactive substance chelation content formation tank/solvent extraction, in which the chelating agent and organic solvent addition device are connected by an inlet pipe, the aqueous phase impulse pipe and organic solvent phase outgoing pipe are spaced apart below. Each end is connected, and the other end of the aqueous layer outlet pipe is connected to the lft of electrolytic ml solution.
1. A radioactive waste liquid processing apparatus, characterized in that the other end of the solvent extraction tank is connected to a distillation purification apparatus. (10) The radioactive waste liquid treatment apparatus according to claim 9, wherein the horizontal compression chamber is an evaporation concentration tank equipped with a heating can. (11) The radioactive waste liquid treatment device according to claim 9, wherein the gear device is a reverse osmosis concentration device. (12) The radioactive waste liquid treatment device according to claim 9, wherein the concentration device is an electrodialysis concentration device.
JP9252782A 1982-05-31 1982-05-31 Method and device for processing radioactive liquid waste Pending JPS58208700A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9252782A JPS58208700A (en) 1982-05-31 1982-05-31 Method and device for processing radioactive liquid waste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9252782A JPS58208700A (en) 1982-05-31 1982-05-31 Method and device for processing radioactive liquid waste

Publications (1)

Publication Number Publication Date
JPS58208700A true JPS58208700A (en) 1983-12-05

Family

ID=14056811

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9252782A Pending JPS58208700A (en) 1982-05-31 1982-05-31 Method and device for processing radioactive liquid waste

Country Status (1)

Country Link
JP (1) JPS58208700A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015152580A (en) * 2014-02-19 2015-08-24 国立大学法人 新潟大学 Recovery method and recovery system of radioactive cesium using chlorofluorocarbon group

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015152580A (en) * 2014-02-19 2015-08-24 国立大学法人 新潟大学 Recovery method and recovery system of radioactive cesium using chlorofluorocarbon group

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