JPH0356900A - Separation of radioactive nuclide - Google Patents

Separation of radioactive nuclide

Info

Publication number
JPH0356900A
JPH0356900A JP19154989A JP19154989A JPH0356900A JP H0356900 A JPH0356900 A JP H0356900A JP 19154989 A JP19154989 A JP 19154989A JP 19154989 A JP19154989 A JP 19154989A JP H0356900 A JPH0356900 A JP H0356900A
Authority
JP
Japan
Prior art keywords
liquid
treated
radionuclides
diffusion dialysis
nuclides
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
JP19154989A
Other languages
Japanese (ja)
Inventor
Takashi Miyake
崇史 三宅
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP19154989A priority Critical patent/JPH0356900A/en
Publication of JPH0356900A publication Critical patent/JPH0356900A/en
Pending legal-status Critical Current

Links

Landscapes

  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

PURPOSE:To allow the adequate management meeting respective cases by separating a specific radioactive nuclide from other radioactive nuclides and separately forming the waste bodies corresponding to the length of a half-life. CONSTITUTION:A diffusion dialysis cell 1 is divided by diffusion dialysis membrane 2 to two chambers so that a liquid 3 to be treated contg. the radioactive nuclides flows in upward current in the left chamber and a recovered liquid 4 flows in downward current in the right chamber. For example, stable Ni<2+> having a sufficiently high concn. is added as a stable isotope 5 to the inlet of the diffusion dialysis cell 1 of the recovery side liquid 4 when the <63>Ni<2+> contained in the liquid to be treated is going to be separated from the other nuclides (R), such a <60>Co<2+>, <90>Sr<2+> and <137>Cs<+>. Both of the liquid 3 to be treated and the recovered liquid 4 are preferably made acidic in such a manner that the stable isotope 5 to be added exists sufficiently as an ion when the cations are separated from each other as in this case. For example, the addition of a small amt. of sulfuric acid to the liquids on both sides suffices.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は元素の異なる2種以上の放射性核種をそれぞれ
の核種に分離する方法に関し、特に原子力施設にて発生
する放射性廃液中の放射性核種を分離する方法に関する
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a method for separating two or more types of radionuclides of different elements into their respective nuclides, and in particular, a method for separating radionuclides in radioactive waste liquid generated at nuclear facilities. Concerning how to separate.

〔従来の技術〕[Conventional technology]

原子力発電プラントで発生している放射性廃液は一般に
低レベル放射性であり、各抽の放射性核種を含んでいる
。これに対する従来の処理技術は第3図に示すように、
まず、必要に応じ放射性廃液中の懸濁固形分すなわち固
体状の粒子を濾過により分離する。分離された粒子は濾
過装置のフィルタエレメントと共に、又は逆流により粒
子濃度の高い液として取り出され、そのままドラム缶詰
、あるいはセメントなどと共にドラム缶内に固化され、
廃棄体となる。この固体状粒子の除去は、これに続く廃
棄物の減容のためのS縮操作に支障とならなければ省略
可能である。
Radioactive waste fluids generated by nuclear power plants are generally low-level radioactive and contain various types of radionuclides. The conventional processing technology for this is shown in Figure 3.
First, if necessary, suspended solids, that is, solid particles, in the radioactive waste liquid are separated by filtration. The separated particles are taken out together with the filter element of the filtration device or as a liquid with a high particle concentration by backflow, and solidified in a drum can or with cement, etc.
It becomes a waste body. Removal of the solid particles can be omitted if it does not interfere with the subsequent S-condensation operation for reducing the volume of the waste.

次に、廃棄物発生量低減の観点から謀縮操作が行なわれ
減容された濃縮廃液となる。この濃縮操作は一般に加熱
蒸発により水分を蒸発することにより行なわれる。濃縮
廃液はセメント、ボリマーなどでドラム缶内に固化され
廃棄体となる。固化の一手法であるアスファルト固化の
場合には、それだけの操作で、水分蒸発すなわち、濃縮
操作と固化が同時に行なわれる。
Next, from the viewpoint of reducing the amount of waste generated, a reduction operation is performed to obtain a concentrated waste liquid whose volume is reduced. This concentration operation is generally carried out by evaporating water by heating and evaporating. Concentrated waste liquid is solidified in a drum with cement, polymer, etc. and becomes waste. In the case of asphalt solidification, which is one of the solidification methods, water evaporation, that is, concentration operation, and solidification are performed simultaneously with just one operation.

これら低レベル放射性廃液の主或分は、例えば、PWR
原子力発電プラントの場合にはホウ酸であり、B WR
原子力発電プラントの場合には芒硝であり、放射性核種
及びその同位体の濃縮(よ極めて低い。
The main part of these low-level radioactive waste liquids is, for example, PWR.
In the case of nuclear power plants, it is boric acid, BWR
In the case of nuclear power plants, it is mirabilite, which has a very low concentration of radionuclides and their isotopes.

廃棄体に含まれる放射性核種(放射性物質の種類と同義
語)毎に、その許容限度濃度が定められる見込みであり
、放射性核種でもその濃度を超えればプラントサイト外
に搬出できなくなる。ところが、従来方法では発生する
廃液を放射性核種の存在比をそのままに濃縮しているた
め、プラントサイト外に搬出できなくなる可能性が高か
った。
It is expected that a permissible concentration limit will be established for each radionuclide (synonymous with the type of radioactive substance) contained in waste, and even radionuclides will no longer be able to be transported outside the plant site if their concentration exceeds that concentration. However, in the conventional method, the generated waste liquid is concentrated without changing the abundance ratio of radionuclides, so there is a high possibility that it will not be able to be transported outside the plant site.

又、廃棄体管理の観点からも、半減期の種々の放射性核
種が混在していると、どの廃棄体も長半減期放射性核種
が十分減衰するまで管理しなければならない。
Also, from the perspective of waste management, if radionuclides with various half-lives are mixed, each waste must be managed until the radionuclides with long half-lives have sufficiently decayed.

ちなみに、「核原料物質、核燃料物質及び原子炉の規則
」に関する法律施行令〔昭和32年11月21日政令第
324号、改正昭和62年3月17日政令第41号〕に
は、その埋没を行う時以後における放射性物質と、その
超えないものとする濃度が次表の如く定められている1
,〔発明が解決しようとする課題〕 従来の放射性廃液の処理方法では濃縮による廃棄物の減
容のみを行なうため、元来放対性廃液に含まれる放射性
核種がそのまま濃縮される。
By the way, the Enforcement Order of the Act on "Regulations for Nuclear Source Materials, Nuclear Fuel Materials and Nuclear Reactors" [Cabinet Order No. 324 of November 21, 1950, revised Cabinet Order No. 41 of March 17, 1988] states that The radioactive substances and their concentrations that shall not be exceeded after the time of carrying out are determined as shown in the following table1.
, [Problems to be Solved by the Invention] In the conventional radioactive waste liquid treatment method, only the volume of the waste is reduced by concentration, so that the radionuclides originally contained in the radioactive waste liquid are concentrated as they are.

従って、その中の1核種でも許容限度濃度を超えればプ
ラントサイトから搬出できなくなる。
Therefore, if even one of the nuclides exceeds the permissible limit concentration, it will no longer be possible to transport them from the plant site.

又、廃棄体の管理程度も全数について長半減期核種が減
衰するまで厳密に行なう必要がある。
Furthermore, it is necessary to strictly manage all waste materials until long-half-life nuclides are attenuated.

本発明では、これらの課題の解決のために、長半減期核
種を選択的に分離することができるような放射性核種の
分離方法を提供しようとするものである。
In order to solve these problems, the present invention aims to provide a method for separating radionuclides that can selectively separate long half-life nuclides.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は各種放射性核種を含む被処理液と回収側液を拡
散透析膜を介して対向流で流し、被処理液中の分離しよ
うとする特定の放射性核種の安定な同位体を該被処理液
中の放射性核種と同じ存在形態で回収側液に添加し、該
被処理液中の11コ1定の放射性核種を他の放射性核挿
から分雑ずることを特徴とする放射性核種の分離方法で
ある。
In the present invention, a liquid to be treated and a recovery side liquid containing various radionuclides are caused to flow in countercurrents through a diffusion dialysis membrane, and stable isotopes of a specific radionuclide to be separated in the liquid to be treated are separated from the liquid to be treated. A method for separating radionuclides, which is characterized in that the radionuclides are added to the recovery liquid in the same existing form as the radionuclides in the liquid, and the 11 radionuclides in the liquid to be treated are separated from other radionuclides. be.

〔 f乍ハ] 〕[ f乍は] 〕

拡散透析膜を介して、ある存在形態の元素につき濃度差
があれば、濃度の高い方から低い方へ移動する。この移
動は元素及びその存在形態の種類毎に起こり、その1つ
の元素及び存在形態では同位体間の差異は無視できる。
If there is a difference in the concentration of an element in a certain existing form, the element moves from the higher concentration to the lower concentration through the diffusion dialysis membrane. This movement occurs for each type of element and its existing form, and the difference between isotopes can be ignored for one element and its existing form.

従って、被処理液中に含まれる元素(放射性核種を含む
ことは勿論である)は回収側の元素濃度が低い場合は拡
敗透析膜を介して回収側へ移動する。
Therefore, if the element concentration on the recovery side is low, the elements contained in the liquid to be treated (including radionuclides, of course) will move to the recovery side via the dialysis membrane.

回収側液の元素濃度が被処理液側の同一存在形遮のそれ
より高ければ逆に回収側液から被処理液側への元素の移
動が起こる。
If the concentration of an element in the recovery liquid is higher than that of the same existing type in the liquid to be treated, conversely, the element will migrate from the liquid to be treated to the liquid to be treated.

従って、回収側液に分離しようとする核種の安定な同位
体を、被処理液側のその元素の濃度より十分高い濃度(
例えば被処理液の10倍の濃度)となるように、被処理
液側と同じ存在形態で添加すると、その分離しようとず
る核種は被処理液側から回収.側へ移動せず、逆にその
安定な同位体が回収側から被処理液側へ移動する。
Therefore, the stable isotope of the nuclide to be separated into the recovery liquid can be contained at a sufficiently higher concentration (
For example, if the nuclide is added in the same form as the liquid to be treated, so that the concentration is 10 times that of the liquid to be treated, the nuclide that attempts to separate will be recovered from the liquid to be treated. On the contrary, the stable isotope moves from the recovery side to the liquid to be treated.

一方、その他の核種は濃度差により被処理液側から回収
側へ移動する。その結果、分離しようとする核種を含む
元素のみが被処理液中に残る。
On the other hand, other nuclides move from the liquid to be treated side to the recovery side due to the difference in concentration. As a result, only the elements containing the nuclide to be separated remain in the liquid to be treated.

即ち分離できることになる。In other words, they can be separated.

〔実施例〕〔Example〕

〔実施例l〕 実施例を第I図に基づいて説明する。 [Example 1] An embodiment will be described based on FIG.

拡散透析槽1は拡散透析膜2により2室にわけられてお
り、放射性核種を含む被処理液3が左室を」二向流にて
流れ、回収側液4が右室を下向流で流れるようになって
いる。
The diffusion dialysis tank 1 is divided into two chambers by a diffusion dialysis membrane 2. The liquid to be treated 3 containing radionuclides flows in the left ventricle in a two-way flow, and the recovery liquid 4 flows in the right ventricle in a downward flow. It's flowing.

例えば被処理液中に含まれる6J12+を6 0 [:
 o 2 +!lOSr2+ ,  137c,+など
他の核種(これらをまとめてRと略記する)から分離し
ようとする場合{,は、回収側液4の拡散透析槽1人口
に1一分高い濃度で安定なNi2+を安定同位体5とし
て添加4゛る。この場合のように陽イオン同士を分離す
る場合には、添加する安定同位体5が十分イ才7・とじ
て存在するように、被処理液3、回収側イ÷・、4共に
酸性とすることが望ましい。例えば、i”1τ1t酸を
少量、両側液に添加すればよい。なお、両側液の例えば
硫酸濃度が同じであれば拡散透析膜2を介しての硫酸の
移動はなくなる。例え1χ、被処理液3が2N硫酸水溶
液に種々核種がイ゛4゛ンとして存在している場合、回
収側液も2N (1j:j酸水溶液であれば硫酸の拡販
透析膜を介しての移動は起こらない。拡散透析v2とし
て陽イオンを選択的に透析する陽イオン交換j摸を用い
る。
For example, 6J12+ contained in the liquid to be treated is 60[:
o 2 +! When trying to separate from other nuclides such as lOSr2+, 137c, + (these are collectively abbreviated as R), stable Ni2+ is added to one population of the diffusion dialysis tank of the recovery side liquid 4 at a high concentration for 1 minute. There is 4 added as a stable isotope 5. When separating cations as in this case, both the liquid to be treated 3 and the recovery side A, 4 are made acidic so that the stable isotope 5 to be added is present in a sufficient amount. This is desirable. For example, a small amount of i"1τ1t acid may be added to the liquids on both sides. If the concentrations of sulfuric acid in both liquids are the same, there will be no movement of sulfuric acid through the diffusion dialysis membrane 2. For example, if 1χ, the liquid to be treated When various nuclides exist as ions in a 2N sulfuric acid aqueous solution, the recovery side liquid is also a 2N (1j:j acid aqueous solution), so that sulfuric acid does not migrate through the dialysis membrane. Diffusion A cation exchange model that selectively dialyzes cations is used as dialysis v2.

安定なN12゛の添加形態としてはこの坦合NiS[)
4の水溶液が望ましいが、NiCh , Ni(N[]
.)2等の水溶液等NiがNl2+とじて存在すれば{
11fでもよい。
This supported NiS[) is a stable addition form of N12゛.
An aqueous solution of 4 is preferable, but NiCh, Ni(N[]
.. )2 etc., if Ni exists as Nl2+, {
11f may be sufficient.

拡散透析槽の構造は模式的に第1図に拡散透析膜をl枚
有するものを示したが、実川的には処理量増大のため拡
散透析膜面積を増加させる必要があり、第2図に示すよ
うに複数の拡散透析膜を有ずる構造をとる。即ち、拡H
&透析膜2を介して被処理液3と回収側液4が交1[に
対向流で流れるにうにすることが一般的である。
The structure of a diffusion dialysis tank is schematically shown in Figure 1 as having one diffusion dialysis membrane, but in reality it is necessary to increase the area of the diffusion dialysis membrane to increase the throughput. As shown, it has a structure with multiple diffusion dialysis membranes. That is, the expansion H
It is common that the liquid to be treated 3 and the liquid on the recovery side flow through the dialysis membrane 2 in countercurrent flow.

なお、運転条件及び分離しようとする核匪の種類により
回収側液に添加する安定同位体の量は異なるが、一般的
に被処理液側の濃度の約10倍の濃度となるように安定
同位体を添加ずれば十分である。
The amount of stable isotope added to the recovery side liquid varies depending on the operating conditions and the type of nuclear power to be separated, but in general, the stable isotope is added so that the concentration is about 10 times that of the liquid to be treated. It is sufficient to add the body.

〔発明の効果〕〔Effect of the invention〕

本発明により、特定の放射性核種を他の放射性核種から
分離することにより、次の効果が得4 られる。
According to the present invention, the following effects can be obtained by separating specific radionuclides from other radionuclides.

(1)  ’f−減期の長さに応じた廃棄体を別々に作
或することができるようになり、各廃棄体の管J!11
!期間を区分でき、各々に応じた適切フエ管理が行なえ
るようになる。
(1) It is now possible to create separate waste bodies according to the length of the f-life period, and the pipe J for each waste body is now possible! 11
! Periods can be divided and appropriate management can be carried out according to each period.

(2)許容限度濃度を超える核種を除上ずることにより
、それから作威した廃棄体をプラントヅイト外に搬出可
能となる。
(2) By removing nuclides exceeding the permissible limit concentration, the waste produced therefrom can be transported outside the plant.

(3)核種の性質毎に分離した廃棄体を作戊することが
できる、例えば核抽毎に最適な同化方法が存在する場合
には、それらの方法がとれる。あるいは線源の種類や強
度毎に分類した廃棄体を作戒できる。これにより、各廃
棄体に最適な管理ができるようになり、安全性、経済性
等すべてに優れることとなる。
(3) If there is an optimal assimilation method for each type of nuclide, for example, if there is an optimal assimilation method for each type of nuclear extraction, that method can be used. Alternatively, waste can be sorted by type and intensity of radiation source. This makes it possible to optimally manage each waste, resulting in superior safety, economy, and other aspects.

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

第1図は本発明の一実施例を行う装置の模式図、第2図
は本発明に用いる拡散透析柚の実用的な模式図、第3図
は従来の放射性核種の処理系統を示す系統図である。
Fig. 1 is a schematic diagram of an apparatus for carrying out an embodiment of the present invention, Fig. 2 is a practical schematic diagram of diffusion dialysis yuzu used in the present invention, and Fig. 3 is a system diagram showing a conventional radionuclide processing system. It is.

Claims (1)

【特許請求の範囲】[Claims] 各種放射性核種を含む被処理液と回収側液を拡散透析膜
を介して対向流で流し、被処理液中の分離しようとする
特定の放射性核種の安定な同位体を該被処理液中の放射
性核種と同じ存在形態で回収側液に添加し、該被処理液
中の特定の放射性核種を他の放射性核種から分離するこ
とを特徴とする放射性核種の分離方法。
The liquid to be treated and the recovery side liquid containing various radionuclides are flowed in countercurrents through a diffusion dialysis membrane, and the stable isotope of the specific radionuclide to be separated in the liquid to be treated is isolated from the radioactivity in the liquid to be treated. 1. A method for separating radionuclides, which comprises adding radionuclides to a recovery liquid in the same form as the nuclides, and separating specific radionuclides in the liquid to be treated from other radionuclides.
JP19154989A 1989-07-26 1989-07-26 Separation of radioactive nuclide Pending JPH0356900A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19154989A JPH0356900A (en) 1989-07-26 1989-07-26 Separation of radioactive nuclide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19154989A JPH0356900A (en) 1989-07-26 1989-07-26 Separation of radioactive nuclide

Publications (1)

Publication Number Publication Date
JPH0356900A true JPH0356900A (en) 1991-03-12

Family

ID=16276525

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19154989A Pending JPH0356900A (en) 1989-07-26 1989-07-26 Separation of radioactive nuclide

Country Status (1)

Country Link
JP (1) JPH0356900A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007077571A1 (en) * 2006-01-06 2007-07-12 Saha Institute Of Nuclear Physics Separation of no-carrier-added thallium radionuclides from no-carrier-added lead and mercury radionuclides by dialysis
US11510555B2 (en) 2017-12-27 2022-11-29 Hoya Corporation Raising base and endoscope

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007077571A1 (en) * 2006-01-06 2007-07-12 Saha Institute Of Nuclear Physics Separation of no-carrier-added thallium radionuclides from no-carrier-added lead and mercury radionuclides by dialysis
US7799226B2 (en) 2006-01-06 2010-09-21 Saha Institute Of Nuclear Physics Separation of no-carrier-added thallium radionuclides from no-carrier-added lead and mercury radionuclides by dialysys
US11510555B2 (en) 2017-12-27 2022-11-29 Hoya Corporation Raising base and endoscope

Similar Documents

Publication Publication Date Title
Harjula et al. Industrial scale removal of cesium with hexacyanoferrate exchanger—process development
US4302424A (en) Isotope separation
US10480045B2 (en) Selective regeneration of isotope-specific media resins in systems for separation of radioactive isotopes from liquid waste materials
US4983302A (en) Complex preparation-process for decreasing the non-radioactive salt content of waste solutions of nuclear power stations
JP3009828B2 (en) High volume solidification method for high level radioactive liquid waste
US20210024365A1 (en) Systems and Methods for Separating Radium from Lead, Bismuth, and Thorium
CN110349689B (en) Nuclear power plant radioactive waste liquid treatment device
RU2112289C1 (en) Method for recovery of liquid radioactive wastes
KR20250002760A (en) Step-by-step chemical separation method and system using resin packing column
JPH0356900A (en) Separation of radioactive nuclide
JPH08271692A (en) Treatment method of radioactive waste liquid
JPS6245301A (en) Radioactive organic solvent ion processing equipment
Arnal et al. Declassification of radioactive waste solutions of iodine (I125) from radioimmune analysis (RIA) using membrane techniques
Geng et al. Treatment of wastewater by nanofiltration-ion exchange technology in uranium conversion process
JP2925413B2 (en) Treatment of radioactive liquid waste
RU2680507C1 (en) Contaminated with tritium waters purification method
JP3099019B2 (en) Selective back-extraction separation method for neptunium
CN116453729A (en) A treatment method and system for radioactive waste liquid produced by accelerator production of medical isotopes
JPS61116695A (en) Method of treating aqueous solution containing radioactive iodine
Mathur et al. Diffusion dialysis aided electrodialysis process for concentration of radionuclides in acid medium
JP2004028903A (en) Device for separating radioactive waste liquid and disposal system for radioactive ion exchange resin provided with the same
JPS61254899A (en) Method of processing radioactive ion exchange resin
Campbell et al. Low-level liquid waste decontamination by ion exchange
Kozlov et al. Development of a process for cesium recovery from the clarified phase of high-level waste storage tanks of the Mayak Production Association with a ferrocyanide sorbent
JP2549155B2 (en) Radioactive waste liquid treatment equipment