JPS6042698A - Method of vitrifying radioactive waste - Google Patents

Method of vitrifying radioactive waste

Info

Publication number
JPS6042698A
JPS6042698A JP15139283A JP15139283A JPS6042698A JP S6042698 A JPS6042698 A JP S6042698A JP 15139283 A JP15139283 A JP 15139283A JP 15139283 A JP15139283 A JP 15139283A JP S6042698 A JPS6042698 A JP S6042698A
Authority
JP
Japan
Prior art keywords
auxiliary agent
radioactive
radioactive waste
mixture
melting
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
JP15139283A
Other languages
Japanese (ja)
Inventor
一郎 乃村
橋本 靖郎
伸二 高橋
長屋 喜一
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 Zosen Corp
Original Assignee
Hitachi Zosen Corp
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 Zosen Corp filed Critical Hitachi Zosen Corp
Priority to JP15139283A priority Critical patent/JPS6042698A/en
Priority to DE19843409803 priority patent/DE3409803A1/en
Priority to FR8405283A priority patent/FR2550879B1/en
Publication of JPS6042698A publication Critical patent/JPS6042698A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21FPROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F9/00Treating radioactively contaminated material; Decontamination arrangements therefor
    • G21F9/28Treating solids
    • G21F9/30Processing
    • G21F9/301Processing by fixation in stable solid media
    • G21F9/302Processing by fixation in stable solid media in an inorganic matrix
    • G21F9/305Glass or glass like matrix

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • 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】 本発明は原子力発電所(BWR)等から発生する放射性
廃棄物のガラス化方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for vitrifying radioactive waste generated from nuclear power plants (BWR) and the like.

従来、原子力発電所で発生した可燃性廃棄物や使用済イ
オン交換樹脂は減容のため焼却炉により焼却され、その
焼却灰はそのままの形でドラム缶詰めにされている。ま
た、濃縮廃液はこのままの形(液体)では長期保管が困
難であるのでセメントやアスファルトと混練した後、ド
ラム缶に流しく1) 込んで固化体とされている。ところで、これら放射性廃
棄物は将来陸地処分または海洋処分される予定である。
Conventionally, combustible waste and used ion exchange resins generated at nuclear power plants are incinerated in an incinerator to reduce their volume, and the incinerated ash is directly canned in drums. In addition, since it is difficult to store concentrated waste liquid for a long time in its current form (liquid), it is mixed with cement or asphalt and then poured into drums1) to form a solidified product. By the way, these radioactive wastes are scheduled to be disposed of on land or in the ocean in the future.

したがって、処分されるまで長期間にわたって施設内で
保管されることになる。そこで何らかの処理を行って放
射性廃棄物を、減容比に優れた、また化学的物理的に安
定で、熱にも強く、内部に含まれる放射性物質を外部に
洩らさない固化体とすることが望ましい。ここで減容比
は処理後の体積と処理前の体積の比でおり、減容比に優
れたとはこの値が小さいことである。しかしながら、従
来の放射性廃棄物の処理方法によると、焼却灰はドラム
缶にそのまま詰められているのでドラム缶が破れた場合
に焼却灰が飛散じ、放射能汚染を来す虞れがあ)、一方
、濃縮廃液の七メン問題があった。
Therefore, they will be stored in the facility for a long period of time until they are disposed of. Therefore, some kind of treatment is performed to turn the radioactive waste into a solidified substance that has an excellent volume reduction ratio, is chemically and physically stable, is resistant to heat, and does not leak the radioactive substances contained inside. is desirable. Here, the volume reduction ratio is the ratio of the volume after treatment to the volume before treatment, and an excellent volume reduction ratio means that this value is small. However, according to conventional radioactive waste disposal methods, incinerated ash is packed directly into drums, so if the drums break, the incinerated ash may scatter, causing radioactive contamination). There was a seven-year problem with concentrated waste liquid.

本発明はこのような問題を解決すること番目的とし、原
子力発電所等から発生する放射性廃棄物の濃縮廃液の乾
燥固型分と、 5in2を主成分とする(2) 助剤と、黒鉛等の炭素を主成分とする反応促進剤とを混
合し、この混合物を溶融炉で高温で溶融し、生成された
ガラス質の物質に放射性物質を封入させた状態で容器に
流し込んで固化する構成の放射性廃棄物のガラス化方法
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、これにより、放射性廃棄物を減容比に優れ、化学的
物理的に安定で、熱にも強く内部に含まれる放射性物質
を外に漏らさないガラス固化体とすることができるもの
である。
The purpose of the present invention is to solve such problems, and the present invention aims to solve these problems by combining the dried solid content of concentrated waste liquid of radioactive waste generated from nuclear power plants, etc., (2) an auxiliary agent mainly composed of 5in2, and graphite, etc. The mixture is mixed with a reaction accelerator whose main component is carbon, the mixture is melted at high temperature in a melting furnace, and the resulting glassy material is filled with radioactive materials and poured into a container where it solidifies. This objective is achieved by providing a method for vitrifying radioactive waste, which enables radioactive waste to be converted into a vitrification method that has excellent volume reduction ratios, is chemically and physically stable, and is resistant to heat. It can be made into a vitrified material that does not leak radioactive substances.

以下本発明の方法を、その−実施例を示す図面に基づい
て詳細に説明する。図において、(1)は原子力発電所
から発生した放射性の濃縮廃液(固形公約20〜25%
でそのほとんどがNa25o4)を乾燥機(図示せず)
により乾燥して得られた乾燥塩、(田は原子力発電所で
発生した可燃性廃棄物や使用済イオン交換樹脂等を焼却
炉(図示せず)により焼却して得られた焼却灰と粘土と
を混合したものまたは粘土等によるいずれもSiO2を
主成分とする助剤、(3)は黒鉛等の戻素を主成分とす
る反応促進剤(3) を示す。(4)は前記乾燥塩(1)を投入される乾燥塩
ホッパ、(5)は前記助剤(2)を投入される助剤ホッ
パ、(6)は前記反応促進剤を投入される反応促進剤ホ
ッパで、それぞれ下端にフィーダ(7) (8) (9
)を設けられている。C1は各ホッパ(4) (5) 
(6)からフィーダ(7) (8)(9)を通して供給
された乾燥塩(1)、助剤(2)および反応促進剤(3
)を所定の混合比になるように計量する計量ホッパ、0
1)は計量ホッパ(10で計量された乾燥塩(1)、助
剤(2)および反応促進剤(3)を混合する混合機、@
は混合機(11)から払い出された混合物を投入される
供給ホッパで、該供給ホッパOnの下端にはスクリュー
フィーダα3が設けられている。α荀は前記供給ホッパ
(至)からスクリューフィーダ(至)を通して混合物を
連続供給される溶融炉、(至)は該溶融炉α荀で生成さ
れた溶融ガラス0・を流し込まれてこれを固化する同化
容器、(17)は溶融炉α滲で発生したS02゜C02
等の排ガスを示す。
The method of the present invention will be explained in detail below based on the drawings showing embodiments thereof. In the figure, (1) is radioactive concentrated waste liquid (approximately 20 to 25% solid waste) generated from nuclear power plants.
(most of which is Na25o4) in a dryer (not shown)
Dry salt obtained by drying (Tada), incineration ash and clay obtained by incinerating combustible waste and used ion exchange resin etc. generated at nuclear power plants in an incinerator (not shown). (3) is a reaction accelerator (3) whose main component is a return element such as graphite. 1) is a dry salt hopper into which the auxiliary agent (2) is fed, (5) is an auxiliary agent hopper into which the auxiliary agent (2) is fed, and (6) is a reaction accelerator hopper into which the reaction accelerator is fed, each with a feeder at the lower end. (7) (8) (9
) is provided. C1 is each hopper (4) (5)
Dry salt (1), auxiliary agent (2) and reaction accelerator (3) fed from (6) through feeder (7) (8) (9)
) to a predetermined mixing ratio, a weighing hopper, 0
1) is a mixer for mixing weighed dry salt (1), auxiliary agent (2) and reaction accelerator (3) in a weighing hopper (10), @
is a supply hopper into which the mixture discharged from the mixer (11) is fed, and a screw feeder α3 is provided at the lower end of the supply hopper On. The α unit is a melting furnace to which a mixture is continuously supplied from the supply hopper through the screw feeder, and the molten glass produced in the melting furnace α is poured into the melting furnace to solidify it. Assimilation vessel, (17) is S02°C02 generated in the melting furnace α leakage.
Indicates exhaust gas such as

係る構成で、先ず乾燥塩(1)、助剤(2)および反応
促進剤(3)を各ホッパ(4) (5) (6)から計
量ホッパa1に順番に供給し、所定の混合比になるよう
に計量する。
With this configuration, first, dry salt (1), auxiliary agent (2), and reaction accelerator (3) are sequentially supplied from each hopper (4) (5) (6) to weighing hopper a1, and the mixture is adjusted to a predetermined mixing ratio. Weigh it so that it is.

(4) このとき、各成分の割合は溶融固化によって生成するガ
ラスの性質に大きな影響を与えるため、ある範囲の混合
比にしなければならない。先ず第1に、助剤(2)の量
は、乾燥塩(1)の1〜2倍とする。
(4) At this time, since the ratio of each component has a great influence on the properties of the glass produced by melting and solidification, the mixing ratio must be within a certain range. First of all, the amount of auxiliary agent (2) is 1 to 2 times the amount of dry salt (1).

これよりも助剤(2)が少ないと溶融の際に未反応の乾
燥塩(1)が残り、反対にこれよりも助剤(2)が多い
と充分なガラス化反応を起こすことができなくなる。な
お助剤(2)に使用する粘土は、ガラスの性質向上のた
め、5〜20%程度のアルミナ等の安定酸化物を含んで
いるものが良い。また、粘土と焼却灰を混入する助剤(
2)の場合、焼却灰の混合割合は混合後の助剤(2)の
重量の30%を限度とする。焼却灰はS t O2を主
成分とし残りはFe 20.5 、]fun 3()□
等の安定酸化物であるので、生成するガラスの網目構造
の中に取込まれガラスの性質を向上させる働きをなす。
If the amount of auxiliary agent (2) is less than this, unreacted dry salt (1) will remain during melting, and on the other hand, if the amount of auxiliary agent (2) is more than this, sufficient vitrification reaction will not occur. . The clay used as the auxiliary agent (2) preferably contains about 5 to 20% of a stable oxide such as alumina in order to improve the properties of the glass. In addition, an auxiliary agent that mixes clay and incineration ash (
In the case of 2), the mixing ratio of incinerated ash is limited to 30% of the weight of the auxiliary agent (2) after mixing. Incineration ash is mainly composed of S t O2 and the rest is Fe 20.5, ]fun 3()□
Since it is a stable oxide such as, it is incorporated into the network structure of the glass that is produced and serves to improve the properties of the glass.

次に、黒鉛等の反応促進剤(3)の蝋は、乾燥塩(1)
の重量の5〜20%程度使用すれば充分である。
Next, the wax of reaction accelerator (3) such as graphite is mixed with dry salt (1).
It is sufficient to use about 5 to 20% of the weight of .

黒鉛を入れない場合、溶融反応に1400’C以上必要
となるのに対し、黒鉛を入れると溶融反応が約1200
℃となり、反応温度の低下、反応速度の向上(5) 等において有効である。計量ホッパαQでこのような混
合比になるように計量し終えると、混合機01)に全量
払い出し、充分に混合する。この後、供給ホッパ(2)
、スクリューフィーダ(至)を通して溶融炉04へ混合
物を連続的に供給する。溶融炉(ロ)で高温溶融された
混合物は溶融ガラスαQとなる。そこで、この溶融ガラ
スαeを固化容器αGに流し込んで固化させる。溶融時
に発生する排ガスaηは排ガス処理設備(図示せず)に
おいて処理する。
If graphite is not added, the melting reaction requires over 1400'C, whereas with graphite, the melting reaction is approximately 1200'C.
℃, which is effective in lowering the reaction temperature and increasing the reaction rate (5). When the measuring hopper αQ finishes measuring the mixture to achieve such a mixing ratio, the entire amount is discharged to the mixer 01) and thoroughly mixed. After this, supply hopper (2)
, the mixture is continuously fed to the melting furnace 04 through the screw feeder (to). The mixture melted at high temperature in the melting furnace (b) becomes molten glass αQ. Therefore, this molten glass αe is poured into a solidification container αG and solidified. The exhaust gas aη generated during melting is treated in an exhaust gas treatment facility (not shown).

次に、実験例を挙げる。混合割合として、乾燥塩36%
、焼却灰5%、粘土(助剤)54%、黒紅反応促進剤)
5%で混合した。その組成は重R%で5in246’l
lJ、Na2SO436%、アルミナ等の酸化物13%
、C5%となった。この混合物を混合機−で均質になる
まで充分混合した。これは、混合が不充分であると生成
ガラスが不良なものとなるためである。
Next, an experimental example will be given. Mixing ratio: 36% dry salt
, incineration ash 5%, clay (auxiliary agent) 54%, black red reaction accelerator)
Mixed at 5%. Its composition is 5in246'l in weight R%
lJ, Na2SO4 36%, oxides such as alumina 13%
, C5%. This mixture was thoroughly mixed with a mixer until it became homogeneous. This is because if the mixing is insufficient, the resulting glass will be inferior.

混合機0刀から供給ホッパ(2)に全量払い出した混合
物はスクリューフィーダ(至)で溶融炉(ロ)へ連続供
給した。フィーダとして特にスクリューフィーダ(至)
を用いたのは、スクリューフィーダ叫は振動フィ(6) −ダ等と異なり振動が少なく混合物を分離する可能性が
少ないからである。溶融炉(14)には溶融ガラス接触
面に電鋳レンガを用いた電気溶融炉を使った。ここで、
約1200’Cで混合物を溶融すると、下記の反応によ
りガラスが生成された。
The entire amount of the mixture discharged from the mixer to the supply hopper (2) was continuously supplied to the melting furnace (2) by the screw feeder (2). Especially screw feeder (to) as a feeder
The reason why a screw feeder was used is that unlike a vibrating feeder, etc., a screw feeder generates less vibration and is less likely to separate the mixture. The melting furnace (14) used was an electric melting furnace using electroformed bricks on the molten glass contact surface. here,
Upon melting the mixture at approximately 1200'C, a glass was produced by the reaction described below.

Na SO+nSiO2+mMOx+C+−H02−=
4 Na ()mMOx−nsi02+S02↑+CO2↑
ここでmMOxは安定酸化物であり、Na2O・ITI
MOX−nSiO2は生成するガラスである。生成した
溶融ガラスullGは反応時に発生するS02.C02
ガスQ7)をガス抜き清澄後、固化容器αQに流し込ん
で固化した。また、SO2,CO2ガスQ71は排ガス
処理設備で処理した。溶融ガラス0!の組成はSin2
6m 、 Na2O21%、安定酸化物16%であった
。以上の手順で製作したガラス同化体についてJIS−
R−3502に規定されるアルカリ溶出試験を行ったと
ころ、アルカリ溶出量2.1mgとなり、並質ガラスと
同等もしくはそれ以上の性能であることが分った。
Na SO+nSiO2+mMOx+C+-H02-=
4 Na ()mMOx-nsi02+S02↑+CO2↑
Here, mMOx is a stable oxide, Na2O・ITI
MOX-nSiO2 is the glass produced. The generated molten glass ullG is S02. generated during the reaction. C02
After gas Q7) was degassed and clarified, it was poured into a solidification container αQ and solidified. Further, SO2 and CO2 gas Q71 were treated with exhaust gas treatment equipment. No molten glass! The composition of is Sin2
6m, Na2O21%, stable oxide 16%. JIS-
When the alkali elution test specified in R-3502 was conducted, the amount of alkali elution was 2.1 mg, and it was found that the performance was equivalent to or better than that of ordinary glass.

以上本発明方法によれば、処理する放射性廃棄物自体を
固化剤の一部とするとともに、溶融の際(7) にSO2,CO2を放出させることができるので、減容
比に優れたガラス固化体を得ることができる。また原子
力発電所等から発生する放射性の濃縮廃液のみならず、
可燃性廃棄物等の焼却灰も同時にガラス同化体とするこ
とができ、至って合理的である。しかも、得られたガラ
ス固化体は化学的物理的に安定で、熱にも強く内部に含
まれる放射性物質を外に漏らす虞れは少ない。
As described above, according to the method of the present invention, the radioactive waste to be treated can itself be used as a part of the solidification agent, and SO2 and CO2 can be released during melting (7), resulting in vitrification with an excellent volume reduction ratio. You can get a body. In addition to radioactive concentrated waste liquid generated from nuclear power plants,
Incineration ash from combustible waste can also be made into glass assimilate at the same time, which is very rational. Moreover, the obtained vitrified material is chemically and physically stable, resistant to heat, and there is little risk of leaking the radioactive substances contained inside.

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

図面は本発明の一実施例を示すフロー図である。 (1)・・・乾燥塩、(2)・・・助剤、(3)・・・
反応促進剤、αη・・・混合機、0→・・・溶融炉、a
G・・・同化容器代理人 森 本 義 弘 (8)
The drawing is a flow diagram showing one embodiment of the present invention. (1)...Dry salt, (2)...Auxiliary agent, (3)...
Reaction accelerator, αη...mixer, 0→...melting furnace, a
G...Assimilation container agent Yoshihiro Morimoto (8)

Claims (1)

【特許請求の範囲】[Claims] 1、原子力発電所等から発生する放射性廃棄物の濃縮廃
液の乾燥固型分と、SiO2を主成分とする助剤と、黒
鉛等の炭素を主成分とする反応促進剤とを混合し、この
混合物を溶融炉で高温で溶融し、生成されたガヲヌ質の
物質に放射性物質を封入させた状想て容器に流し込んで
固化することを特徴とする放射性廃棄物のガラス化方法
1. Mix the dry solid content of concentrated waste liquid of radioactive waste generated from nuclear power plants, etc., an auxiliary agent mainly composed of SiO2, and a reaction accelerator mainly composed of carbon such as graphite. A method for vitrifying radioactive waste, which is characterized by melting a mixture at a high temperature in a melting furnace, and pouring the resulting gas-like material into a container to solidify it, simulating a radioactive substance encapsulated therein.
JP15139283A 1983-08-18 1983-08-18 Method of vitrifying radioactive waste Pending JPS6042698A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP15139283A JPS6042698A (en) 1983-08-18 1983-08-18 Method of vitrifying radioactive waste
DE19843409803 DE3409803A1 (en) 1983-08-18 1984-03-16 Process for the vitrification of radioactive waste
FR8405283A FR2550879B1 (en) 1983-08-18 1984-04-04 PROCESS FOR VITRIFICATION OF RADIOACTIVE WASTE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15139283A JPS6042698A (en) 1983-08-18 1983-08-18 Method of vitrifying radioactive waste

Publications (1)

Publication Number Publication Date
JPS6042698A true JPS6042698A (en) 1985-03-06

Family

ID=15517578

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15139283A Pending JPS6042698A (en) 1983-08-18 1983-08-18 Method of vitrifying radioactive waste

Country Status (3)

Country Link
JP (1) JPS6042698A (en)
DE (1) DE3409803A1 (en)
FR (1) FR2550879B1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62123046A (en) * 1985-11-22 1987-06-04 株式会社神戸製鋼所 Manufacture of hydraulic road bed material
JP2012509458A (en) * 2008-11-10 2012-04-19 エーエルデー・バキューム・テクノロジーズ・ゲーエムベーハー Matrix material of graphite and inorganic binder suitable for final disposal of radioactive waste, and use thereof
JP2014134463A (en) * 2013-01-10 2014-07-24 Toshiba Corp Radioactive waste solidification method, and solidification device therefor

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8502009B2 (en) 2008-11-26 2013-08-06 Ald Vacuum Technologies Gmbh Matrix material comprising graphite and an inorganic binder suited for final disposal of radioactive waste, a process for producing the same and its processing and use

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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
JPS6025499A (en) * 1983-07-21 1985-02-08 日立造船株式会社 Glass solidifying treating method of radioactive waste

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DE3409803A1 (en) 1985-03-07
FR2550879A1 (en) 1985-02-22

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