JPH0151955B2 - - Google Patents
Info
- Publication number
- JPH0151955B2 JPH0151955B2 JP57168794A JP16879482A JPH0151955B2 JP H0151955 B2 JPH0151955 B2 JP H0151955B2 JP 57168794 A JP57168794 A JP 57168794A JP 16879482 A JP16879482 A JP 16879482A JP H0151955 B2 JPH0151955 B2 JP H0151955B2
- Authority
- JP
- Japan
- Prior art keywords
- polymerization
- radioactive waste
- polymerization accelerator
- mixture
- accelerator
- 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.)
- Expired
Links
Landscapes
- Processing Of Solid Wastes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Description
【発明の詳細な説明】
[発明の技術分野]
本発明は熱硬化性樹脂を使用した放射性廃棄物
の固化処理方法に関する。Detailed Description of the Invention [Technical Field of the Invention] The present invention relates to a method for solidifying radioactive waste using a thermosetting resin.
[発明の技術的背景とその問題点]
近年、原子力発電所その他の原子力施設から発
生する放射性廃液を乾燥、粉体化し、この粉体を
熱硬化性樹脂等で固化して処理することが考えら
れている。[Technical background of the invention and its problems] In recent years, it has been considered to dry and powder radioactive waste fluid generated from nuclear power plants and other nuclear facilities, and to treat this powder by solidifying it with thermosetting resin, etc. It is being
しかして、放射性廃棄物中には熱硬化性樹脂の
重合反応を阻害する物質が含まれる場合があり、
例えば沸騰水型原子力発電所で発生する濃縮廃液
の主成分は硫酸ナトリウム(Na2SO4)である
が、この他に微量成分としてCa,Si,Fe,Co,
Ni,Cuといつた元素が往々にして含まれており、
特にCuの水酸化物が存在すると熱硬化性樹脂の
重合反応が著しく阻害されることが判明した。 However, radioactive waste may contain substances that inhibit the polymerization reaction of thermosetting resins.
For example, the main component of concentrated waste fluid generated at boiling water nuclear power plants is sodium sulfate (Na 2 SO 4 ), but other minor components include Ca, Si, Fe, Co,
Often contains elements such as Ni and Cu,
In particular, it was found that the presence of Cu hydroxide significantly inhibits the polymerization reaction of thermosetting resins.
これは銅の水酸化物は両性的性質を有して次式
のように解離し、
Cu(OH)2Cu+++2OH-
Cu(OH)2CuO2 --+2H+
ここで発生するH+は、重合開始剤、重合促進
剤により生ずる一次ラジカルおよびこれに引き続
き発生する連鎖反応におけるラジカルと反応して
ラジカルを不活性化するためであると考えられ
る。 This is because copper hydroxide has amphoteric properties and dissociates as shown in the following formula, Cu(OH) 2 Cu ++ +2OH - Cu(OH) 2 CuO 2 -- +2H + H + generated here This is thought to be due to the reaction with primary radicals generated by the polymerization initiator and polymerization accelerator, and the radicals in the subsequent chain reaction, thereby inactivating the radicals.
このようにラジカル重合により硬化する熱硬化
性樹脂は、ラジカルと反応するH+の発生源、例
えば水酸化銅が存在する場合硬化し難く、放射性
廃棄物と熱硬化性樹脂との混合物は未重合あるい
は硬化不充分のまま貯蔵容器内に貯蔵されること
になる。。この混合物は未重合のままでは放射能
閉じ込め能力はほとんど期待できず、そのうえ未
重合の固化剤は消防法上危険物に分類されたもの
であり、放射性廃棄物をより危険な状態におくこ
とになるという問題があつた。 Thermosetting resins that harden through radical polymerization are difficult to cure in the presence of sources of H + that react with radicals, such as copper hydroxide, and mixtures of radioactive waste and thermosetting resins are difficult to cure when they are not polymerized. Otherwise, it will be stored in a storage container with insufficient hardening. . If this mixture remains unpolymerized, it can hardly be expected to have any radioactivity trapping ability, and the unpolymerized solidifying agent is classified as a dangerous substance under the Fire Service Act, making radioactive waste even more dangerous. There was a problem.
[発明の目的]
本発明はこのような問題を解消するためになさ
れたもので、放射性廃棄物中に硬化反応を妨害す
る物質、例えば水酸化銅が含有されていても硬化
が充分になされる放射性廃棄物の固化処理方法を
提供することを目的とする。[Object of the Invention] The present invention was made to solve these problems, and is capable of sufficiently curing even if the radioactive waste contains substances that interfere with the curing reaction, such as copper hydroxide. The purpose is to provide a method for solidifying radioactive waste.
[発明の概要]
すなわち本発明方法は、水酸化銅または他の両
性物質を含む放射性廃液物に、熱硬化性樹脂、重
合開始剤および重合促進剤を混合して固化するに
あたり、重合促進剤にアルカリ性物質を混合した
ものを重合反応中に使用することを特徴とする。[Summary of the Invention] That is, the method of the present invention involves mixing a thermosetting resin, a polymerization initiator, and a polymerization accelerator into a radioactive waste liquid containing copper hydroxide or other amphoteric substances, and solidifying the mixture. It is characterized in that a mixture of alkaline substances is used during the polymerization reaction.
本発明に使用する熱硬化性樹脂としては、例え
ば無水マレイン酸と無水フタル酸とをプロピレン
グリコールと縮合して得られる不飽和ポリエステ
ルにスチレンのような単量体を混合して得られる
ものがあげられる。この混合物はメチルエチルケ
トンパーオキサイドのような重合開始剤とナフテ
ン酸コバルトのような重合促進剤を添加すると常
温で硬化反応を示す。なお通常ナフテン酸コバル
ト等の重合促進剤はトルエンやミネラルスピリツ
ツ等の溶剤で希釈されて市販されている。 Examples of the thermosetting resin used in the present invention include those obtained by mixing a monomer such as styrene with an unsaturated polyester obtained by condensing maleic anhydride and phthalic anhydride with propylene glycol. It will be done. This mixture exhibits a curing reaction at room temperature when a polymerization initiator such as methyl ethyl ketone peroxide and a polymerization accelerator such as cobalt naphthenate are added. Note that polymerization accelerators such as cobalt naphthenate are usually commercially available after being diluted with a solvent such as toluene or mineral spirits.
本発明に使用するアルカリ性物質としては、重
合促進剤と反応したり、重合促進剤に混合後増粘
を起こしたり、またポンプで移送可能な粘度とす
るのに多量の重合促進剤や希釈剤を使用しなけれ
ばならないものは適切ではない。例えば水酸化カ
ルシウムは重合促進剤であるナフテン酸コバルト
と反応して増粘し供給困難となるので好ましくな
い。酸化マグネシウムは10日放置後粘度が混合直
後の10倍となつて、増粘の性質があるので、この
ようなものは直ちに使い終わる分にはよいが長期
保管ができないという難点がある。いずれにして
も重合促進剤にアルカリ性物質を添加したら常時
撹拌する必要がある。 The alkaline substance used in the present invention may react with the polymerization accelerator, cause thickening after mixing with the polymerization accelerator, or contain a large amount of polymerization accelerator or diluent to achieve a viscosity that can be transferred by a pump. What you have to use is not appropriate. For example, calcium hydroxide is not preferred because it reacts with cobalt naphthenate, which is a polymerization accelerator, and thickens, making it difficult to supply. Magnesium oxide has the property of thickening, becoming 10 times as viscous after being left for 10 days as it was immediately after mixing, so such products are good for immediate use, but have the disadvantage that they cannot be stored for long periods of time. In any case, once the alkaline substance is added to the polymerization accelerator, it is necessary to constantly stir it.
本発明においては移送可能な粘度とするのに希
釈剤を固化体の強度を低下させない範囲で添加し
てもよい。 In the present invention, a diluent may be added to obtain a transportable viscosity within a range that does not reduce the strength of the solidified product.
希釈剤としては、揮発性が小さく、また変質等
がなく長期間安定で、しかも粘度が適当で添加量
の少なくても済むのが望ましい。例えば不飽和ポ
リエステル樹脂、スチレン、ミネラルスピリツ
ツ、トルエン、ジオクチルフタレート等があげら
れる。 As a diluent, it is desirable that it has low volatility, is stable for a long period without deterioration, has an appropriate viscosity, and can be added in a small amount. Examples include unsaturated polyester resin, styrene, mineral spirits, toluene, dioctyl phthalate, and the like.
しかしながら、重合促進剤を長期保存する場合
は、不飽和ポリエステル樹脂は重合促進剤と反応
して硬化するおそれがあるので不適当である。 However, if the polymerization accelerator is to be stored for a long period of time, unsaturated polyester resins are unsuitable because they may react with the polymerization accelerator and harden.
本発明においては、乾燥、粉末化した放射性廃
棄物に熱硬化性樹脂を添加、混合し、さらに重合
促進剤およびアルカリ性物質を混合した重合促進
剤をポンプ等で添加して常温で放置させる。 In the present invention, a thermosetting resin is added to and mixed with dried and powdered radioactive waste, and then a polymerization promoter and a polymerization promoter mixed with an alkaline substance are added using a pump or the like, and the mixture is allowed to stand at room temperature.
[発明の実施例] 次に本発明の実施例について説明する。[Embodiments of the invention] Next, examples of the present invention will be described.
実施例 1
重合促進剤に酸化マグネシウムを1:1の割合
で添加、混合し、この混合物を、硫酸ナトリウム
59重量%と重合開始剤(メチルエチルケトンパー
オキサイド)を1重量%加えた不飽和ポリエステ
ル樹脂を主成分とする熱硬化性樹脂40重量%と水
酸化銅1重量%との混合液に樹脂分に対してアル
カリ性物質が1重量%となるように添加混合し
た。一昼夜放置後強固なプラスチツク固化体が得
られた。Example 1 Magnesium oxide was added to a polymerization accelerator at a ratio of 1:1 and mixed, and this mixture was mixed with sodium sulfate.
59% by weight and 1% by weight of a polymerization initiator (methyl ethyl ketone peroxide) in a mixed solution of 40% by weight of a thermosetting resin whose main component is an unsaturated polyester resin and 1% by weight of copper hydroxide based on the resin content. The alkaline substance was added and mixed to a concentration of 1% by weight. After standing for a day and night, a strong solidified plastic was obtained.
このプラスチツク固化体の表面硬度(シヨア
D)は水酸化銅を含有しない放射性廃棄物の場合
と同程度でほぼ82〜89であつた。 The surface hardness (Shore D) of this solidified plastic was approximately 82 to 89, which was comparable to that of radioactive waste not containing copper hydroxide.
実施例 2
重合促進剤と高活性工業用酸化マグネシウム
(キヨーワマグ#150)とミネラルスピリツツの
1:2:2の混合物に変えた以外は実施例1と同
様にしてプラスチツク固化体を得た。このプラス
チツク固化体の表面硬度は水酸化銅の存在しない
場合と同程度であつた。Example 2 A plastic solidified product was obtained in the same manner as in Example 1, except that a 1:2:2 mixture of the polymerization accelerator, highly active industrial magnesium oxide (Kiyowa Mag #150), and mineral spirits was used. The surface hardness of this plastic solidified body was comparable to that in the absence of copper hydroxide.
[発明の効果]
以上説明したように本発明方法によれば、水酸
化銅のような重合硬化反応を阻害するものが存在
していても硬化が十分行なわれ、強固なプラスチ
ツク固化体が得られる。しかもアルカリ性物質の
添加に際しては、重合促進剤のタンクに撹拌機を
設置したり、高粘度用ポンプを取付けたりして重
合促進剤の注入配管を若干改造するだけでよく、
また液状の混合物としてアルカリ性物質を添加す
るので分散がよく、熱硬化性樹脂や放射性廃棄物
との混和性がよいという利点がある。[Effects of the Invention] As explained above, according to the method of the present invention, even if there is a substance that inhibits the polymerization curing reaction, such as copper hydroxide, curing is carried out sufficiently, and a strong solidified plastic product can be obtained. . Moreover, when adding an alkaline substance, it is only necessary to slightly modify the polymerization accelerator injection piping by installing a stirrer in the polymerization accelerator tank or installing a pump for high viscosity.
Furthermore, since the alkaline substance is added as a liquid mixture, it has the advantage of good dispersion and good miscibility with thermosetting resins and radioactive waste.
Claims (1)
を含む放射性廃棄物に、熱硬化性樹脂、重合開始
剤および重合促進剤を混合して固化するにあた
り、重合促進剤にアルカリ性物質を混合したもの
を重合反応中に使用することを特徴とする放射性
廃棄物の固化処理方法。 2 重合促進剤は液状である特許請求の範囲第1
項記載の放射性廃棄物の固化処理方法。[Claims] 1. When a thermosetting resin, a polymerization initiator, and a polymerization accelerator are mixed and solidified with radioactive waste containing copper hydroxide or a substance that dissociates to generate H + , a polymerization accelerator is used. A method for solidifying radioactive waste characterized by using a mixture of alkaline substances and an alkaline substance during a polymerization reaction. 2 Claim 1 in which the polymerization accelerator is in liquid form
Solidification treatment method for radioactive waste as described in section.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16879482A JPS5958394A (en) | 1982-09-28 | 1982-09-28 | Radioactive waste solidifying method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16879482A JPS5958394A (en) | 1982-09-28 | 1982-09-28 | Radioactive waste solidifying method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5958394A JPS5958394A (en) | 1984-04-04 |
| JPH0151955B2 true JPH0151955B2 (en) | 1989-11-07 |
Family
ID=15874591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16879482A Granted JPS5958394A (en) | 1982-09-28 | 1982-09-28 | Radioactive waste solidifying method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5958394A (en) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2361724A1 (en) * | 1976-08-12 | 1978-03-10 | Commissariat Energie Atomique | STORAGE PROCESS FOR CONTAMINATED ION EXCHANGER RESINS |
-
1982
- 1982-09-28 JP JP16879482A patent/JPS5958394A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5958394A (en) | 1984-04-04 |
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