JPS6025499A - Glass solidifying treating method of radioactive waste - Google Patents
Glass solidifying treating method of radioactive wasteInfo
- Publication number
- JPS6025499A JPS6025499A JP13397683A JP13397683A JPS6025499A JP S6025499 A JPS6025499 A JP S6025499A JP 13397683 A JP13397683 A JP 13397683A JP 13397683 A JP13397683 A JP 13397683A JP S6025499 A JPS6025499 A JP S6025499A
- Authority
- JP
- Japan
- Prior art keywords
- radioactive waste
- treating method
- dry
- clay
- weight
- 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
Links
Landscapes
- Processing Of Solid Wastes (AREA)
- Fertilizers (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】 本発明は放射性廃棄物のカラス同化処理方法に関する。[Detailed description of the invention] The present invention relates to a method for assimilating radioactive waste.
近年、放射性廃棄物の減容化処理を促進する方11(と
じて、放射性廃棄物を)jうス固化体の内部に11Mり
込ませる方法が開発された。この方法は、原子力発電所
(BWR)から発生ずる濃縮廃液(20%程度のNa2
SO4を含む)の乾燥固型分と、5i02を主成分とす
る粘土等の助剤を混合し、これを約1.200℃の高温
で溶融することにより以下のような刀ラス化反応を起こ
させ、その後冷却固化するというものである。In recent years, a method has been developed that promotes the volume reduction treatment of radioactive waste (by closing the radioactive waste) and injecting the radioactive waste into the solidified material. This method uses concentrated waste liquid (approximately 20% Na2) generated from nuclear power plants (BWR).
By mixing the dry solid content (including SO4) with auxiliary agents such as clay containing 5i02 as the main component and melting this at a high temperature of approximately 1.200°C, the following lath-forming reaction occurs. It is then cooled and solidified.
Na2SO4+ nS 102−Na20 ・nS i
02+sO2↑+1021ここで上記ガラス化反応中b
Na2O・r+s+02は窓j3ラス等に使われてい
るソータシリカj3ラスである。Na2SO4+ nS 102-Na20 ・nS i
02+sO2↑+1021 Here, during the above vitrification reaction b
Na2O.r+s+02 is sorter silica j3 lath used for windows j3 lath and the like.
しかしながら、このような乾燥固型分と5i02を主成
分とする粘土等の助剤とのみを混合して溶融する方法に
よると、13ラス化反応の起こる温度が高い、反応速度
が遅い、溶融時に内部に発生するノ5ス(SO□、CO
□)が充分に抜けない等の間l11」1があった。However, according to the method of mixing and melting only such a dry solid content and an auxiliary agent such as clay containing 5i02 as a main component, the temperature at which the 13 lazing reaction occurs is high, the reaction rate is slow, and there are problems during melting. Nose generated inside (SO□, CO
□) was not removed sufficiently.
本発明はこのような問題を解決することを目的とし、原
子力発電所等から発生する放射性廃棄物の乾燥固型分と
、粘土等の5i02を主成分とする助剤の混合物を高温
で溶融し固化する際に、混合物中の乾燥固型分型(よに
対して5重量%以」ニの黒鉛または石炭を前記混合物に
加える構成の放射性廃棄物のカラス固化処理方法を提供
することによって、その目的を達成するものであり、こ
第1.により、ハラス化反応の起こる温度を低く抑える
ことができるとともに反応速度を早めることができ、溶
融時に内部に発生するノjスも充分に抜くことができろ
ものである。The present invention aims to solve such problems by melting at high temperature a mixture of dry solid radioactive waste generated from nuclear power plants and an auxiliary agent mainly composed of 5i02 such as clay. By providing a method for solidifying radioactive waste, the method includes adding graphite or coal in the dry solid form (at least 5% by weight) to the mixture during solidification. This is to achieve the purpose, and with this first step, the temperature at which the halasing reaction occurs can be kept low, the reaction rate can be accelerated, and the nozzles generated inside during melting can be sufficiently removed. It's possible.
以下本発明の方法を、その一実施例を示す図面に基づい
て詳細に説明する。The method of the present invention will be explained in detail below based on the drawings showing one embodiment thereof.
第1図に示すように、先ず原子力発it所(1)から発
生した放射性濃縮廃液(2)を乾燥固形化(:3)する
。As shown in FIG. 1, first, radioactive concentrated waste liquid (2) generated from a nuclear power plant (1) is dried and solidified (3).
これにより乾燥塩(乾燥固形分)(4)が得られる。This gives dry salt (dry solids) (4).
一方、5i02を主成分とする粘土(5)を準備する。On the other hand, clay (5) containing 5i02 as a main component is prepared.
次に、これら乾燥塩(4)と粘土(5)を混合(0)す
る。Next, these dry salts (4) and clay (5) are mixed (0).
このとき乾燥塩(4)の量が少なすぎると混合物は溶f
+cll L、でも充分なj3ラス化反応を起こすこと
ができず、また、乾燥塩(4)の量が多すぎても未反応
の乾4・“v′Il′!、:j (4)が残り不適当で
ある。したがって、乾燥塩(4)の割合は混合物全体の
30〜50重量%が適当である。At this time, if the amount of dry salt (4) is too small, the mixture will become soluble.
+cll L, but sufficient j3 lath formation reaction cannot occur, and even if the amount of dry salt (4) is too large, unreacted dry salt (4) “v′Il′!, :j (4) The remaining portion is inappropriate. Therefore, the appropriate proportion of dry salt (4) is 30 to 50% by weight of the entire mixture.
次に、この混合物に黒鉛(または石炭)(7)を混合物
(11の乾燥塩重量に対して5重量%以上加え、充分に
混合(6)する。Next, graphite (or coal) (7) is added to this mixture in an amount of 5% by weight or more based on the dry salt weight of the mixture (11), and thoroughly mixed (6).
そして、このようにして調合した混合物をマイ90波加
熱、高周波誘導加熱、電気抵抗加熱等の加熱方式を適用
して加熱溶1.8t(sl、容器に流し込んでj5ラス
固化(9)する。これにより)3ラス固化体を形成する
。そして、適宜陸地や海洋に処分θOする。Then, the mixture prepared in this way is heated and poured into a 1.8 t (SL) container using a heating method such as 90 wave heating, high frequency induction heating, electric resistance heating, etc., and is solidified in a j5 lath (9). As a result, a 3 lath solidified body is formed. Then, it is disposed of on land or in the ocean as appropriate.
次に、このような方法による効果を実験結果をもとに説
明する。Next, the effects of such a method will be explained based on experimental results.
先ず、実験1として乾燥塩(4MO爪斌%と粘土60重
量%を混合(6)シた試料を1.050℃〜1.800
℃の温度で1時間加熱(8)シた後、その乾燥塩(4)
と粘土のバうス化反応率を調べた。その結果を示しJこ
ものが第2図である。図からも明らかなように、この程
度の温度ではカラス化反応率がかなり低いことが分かる
。ここでj5ラス化反応率とは分1’i’l! したN
a2SO4の重量に対する最初に混合し1こ乾燥塩の重
量比である。First, as experiment 1, a sample of dry salt (mixture of 4% MO and 60% clay (6)) was heated at 1.050°C to 1.800°C.
After heating for 1 hour at a temperature of °C (8), the dried salt (4)
and the bassing reaction rate of clay. Figure 2 shows the results. As is clear from the figure, the glass formation reaction rate is quite low at this temperature. Here, the j5 lathization reaction rate is 1'i'l! I did N
The weight ratio of the first mixed dry salt to the weight of a2SO4.
次に、実験2として実験1で混合しtこ試料に、その中
の乾燥塩重量に対して5〜50咀!V(%の黒鉛(7)
を加えて1.050℃で1時間加熱(8)シfこ後、そ
の乾燥塩(4)と粘土のカラス化反応率を調べた。その
に、Ii 4,14を示したものが第3図である。図か
らも明らかl、iように黒鉛(7)を5重量%以上加え
ることによりフコラス化反応率は8割を越える程度にな
り、得られtこJlうス固化体も均’IIなものとなっ
た。なお、1t11様な実験結果が、異なる混合物の乾
燥塩(4)と粘にのIJb合物についても、また異なる
温度についても1′:1られtこ。Next, as experiment 2, add 5 to 50 liters of salt to the sample mixed in experiment 1 based on the weight of dry salt in it. V (% graphite (7)
was added and heated at 1.050° C. for 1 hour (8), and the glass formation reaction rate between the dry salt (4) and the clay was examined. In addition, FIG. 3 shows Ii 4 and 14. It is clear from the figure that by adding 5% by weight or more of graphite (7), the fucolasization reaction rate exceeds 80%, and the resulting solidified material is also of a uniform quality. became. It should be noted that similar experimental results were obtained for different mixtures of dry salt (4) and viscous IJb compounds, and also for different temperatures.
以上本発明の方法によれば、Jjガラス化反応起こる7
i14度を低く抑えることができるきともに、反応速度
をfitめることができ、溶融時に内部に発生ずる;j
スも充分に抜くことができる。As described above, according to the method of the present invention, the Jj vitrification reaction occurs.
i14 degrees can be kept low, and the reaction rate can be adjusted to reduce the internal temperature generated during melting; j
It is also possible to sufficiently remove the heat.
図1niは*発明方法を説明するためのもので、第1図
はフロー1>:I 、第2図および第3図は実験結果を
示し、rl)2図は温度と月ラス化反応率の関係を7ノ
′1りねす図、第3図は出船重量(至)とガラス化反応
5Y<の1)、11係をあられす図である。
(1)・・・Ji7子力発電所、(2)・・・放射性濃
縮廃液、(3)・・・乾燥固形1じ、(4)・乾燥塩、
(5)・・・粘土、(6)・・・混合、(ハ 黒鉛、化
)−加熱溶融、(9)・・フ’i :+、717.II
k第1図
1
、[
:;に
一、W、鉛垂量(%2Figure 1ni is for explaining the method of the invention. Figure 1 shows the flow 1>:I, Figures 2 and 3 show the experimental results, and Figure 2 shows the relationship between temperature and lathization reaction rate. Figure 3 is a diagram showing the relationship between ship weight (total) and vitrification reaction 5Y<1), and Figure 11. (1)...Ji7 power plant, (2)...radioactive concentrated waste liquid, (3)...1 tbsp dry solid, (4)...dry salt,
(5)...Clay, (6)...Mixing, (c graphite, chemical) - heating and melting, (9)...F'i: +, 717. II
k Fig. 1, [:; Nii, W, lead amount (%2
Claims (1)
物の乾燥向)Ill、!分と、粘土等の5i02を主成
分とする黒鉛または石炭を前記混合物に加えることを特
徴とする放射性廃棄物のガうス固化処理方法。+, Jl:j子力源V(<Drying of radioactive waste generated from places, etc.) Ill,! 1. A method for gas solidification of radioactive waste, comprising adding to the mixture graphite or coal mainly composed of 5i02, such as clay.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13397683A JPS6025499A (en) | 1983-07-21 | 1983-07-21 | Glass solidifying treating method of radioactive waste |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13397683A JPS6025499A (en) | 1983-07-21 | 1983-07-21 | Glass solidifying treating method of radioactive waste |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6025499A true JPS6025499A (en) | 1985-02-08 |
Family
ID=15117471
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13397683A Pending JPS6025499A (en) | 1983-07-21 | 1983-07-21 | Glass solidifying treating method of radioactive waste |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6025499A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6042698A (en) * | 1983-08-18 | 1985-03-06 | 日立造船株式会社 | Method of vitrifying radioactive waste |
JP2016024121A (en) * | 2014-07-23 | 2016-02-08 | 日立Geニュークリア・エナジー株式会社 | Solidification method of radioactive wastes |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5074100A (en) * | 1973-11-08 | 1975-06-18 | ||
JPS52114900A (en) * | 1976-03-20 | 1977-09-27 | Kernforschung Gmbh Ges Fuer | Method of removing detriment when solidifying radioactive waste liquid |
JPS5728298A (en) * | 1980-06-20 | 1982-02-15 | Kraftwerk Union Ag | Method of finally storing radioactive waste by vitrification |
-
1983
- 1983-07-21 JP JP13397683A patent/JPS6025499A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5074100A (en) * | 1973-11-08 | 1975-06-18 | ||
JPS52114900A (en) * | 1976-03-20 | 1977-09-27 | Kernforschung Gmbh Ges Fuer | Method of removing detriment when solidifying radioactive waste liquid |
JPS5728298A (en) * | 1980-06-20 | 1982-02-15 | Kraftwerk Union Ag | Method of finally storing radioactive waste by vitrification |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6042698A (en) * | 1983-08-18 | 1985-03-06 | 日立造船株式会社 | Method of vitrifying radioactive waste |
JP2016024121A (en) * | 2014-07-23 | 2016-02-08 | 日立Geニュークリア・エナジー株式会社 | Solidification method of radioactive wastes |
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