JPH077109B2 - How to dispose of radioactive waste - Google Patents
How to dispose of radioactive wasteInfo
- Publication number
- JPH077109B2 JPH077109B2 JP61264893A JP26489386A JPH077109B2 JP H077109 B2 JPH077109 B2 JP H077109B2 JP 61264893 A JP61264893 A JP 61264893A JP 26489386 A JP26489386 A JP 26489386A JP H077109 B2 JPH077109 B2 JP H077109B2
- Authority
- JP
- Japan
- Prior art keywords
- exhaust gas
- dust remover
- coating layer
- sulfur
- oxide
- 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 - Lifetime
Links
- 239000002901 radioactive waste Substances 0.000 title claims description 10
- 239000000428 dust Substances 0.000 claims description 28
- 239000011347 resin Substances 0.000 claims description 22
- 229920005989 resin Polymers 0.000 claims description 22
- 239000011247 coating layer Substances 0.000 claims description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 12
- 230000000694 effects Effects 0.000 claims description 12
- 239000011593 sulfur Substances 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 238000006477 desulfuration reaction Methods 0.000 claims description 11
- 230000023556 desulfurization Effects 0.000 claims description 11
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims description 11
- 239000000919 ceramic Substances 0.000 claims description 10
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 9
- 229910052815 sulfur oxide Inorganic materials 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 claims description 6
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 claims description 6
- 229940112669 cuprous oxide Drugs 0.000 claims description 6
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 5
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 4
- 239000000292 calcium oxide Substances 0.000 claims description 4
- 230000002285 radioactive effect Effects 0.000 claims description 4
- 239000011787 zinc oxide Substances 0.000 claims description 4
- 238000001914 filtration Methods 0.000 claims description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 3
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 239000012857 radioactive material Substances 0.000 claims description 2
- 239000007789 gas Substances 0.000 description 23
- 238000002485 combustion reaction Methods 0.000 description 8
- 238000011001 backwashing Methods 0.000 description 3
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 230000003009 desulfurizing effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000941 radioactive substance Substances 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Filtering Materials (AREA)
- Filtering Of Dispersed Particles In Gases (AREA)
- Fertilizers (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は放射性廃棄物を処理する方法に関するもので、
更に詳しくは使用済樹脂の処理に関するものである。TECHNICAL FIELD The present invention relates to a method for treating radioactive waste,
More specifically, it relates to the treatment of used resin.
(従来の技術) 放射性物質取扱施設においては、復水浄化系や廃棄物処
理系の脱塩器から、粉末樹脂、粒状樹脂等の硫黄を含む
使用済樹脂が放射性廃棄物として廃棄される。従来これ
ら使用済樹脂はそのままタンク貯蔵されるかあるいはセ
メント、プラスチック等と混ぜてドラム缶内で固化後保
管されていた。(Prior Art) In radioactive material handling facilities, spent resin containing sulfur such as powder resin and granular resin is discarded as radioactive waste from a demineralizer in a condensate purification system and a waste treatment system. Conventionally, these used resins have been stored in a tank as they are or mixed with cement, plastic, etc., and solidified and stored in a drum can.
(発明が解決しようとする問題点) しかしながら、従来の保管方法では、減容性が劣り、ま
た使用済樹脂は有機物のままであるため化学的に不安定
であった。そこで使用済樹脂も、既に焼却処理されてい
る可燃性雑固体と同様に焼却処理することが考えられる
が、その場合でも次の様な問題点があった。(Problems to be Solved by the Invention) However, in the conventional storage method, the volume reduction property was poor, and the used resin remained an organic substance and was chemically unstable. Therefore, it is possible to incinerate the used resin in the same manner as the combustible miscellaneous solid that has already been incinerated, but even in that case, there were the following problems.
(1) 使用済樹脂の成分であるカチオン樹脂に硫黄が
含まれているため、燃焼排ガス中に硫黄酸化物が発生し
て焼却設備が腐食しやすくなるとともに、大気への放出
ガス中に硫黄酸化物が含まれる。(1) Since sulfur is contained in the cation resin that is a component of the used resin, sulfur oxides are generated in the combustion exhaust gas and the incinerator is easily corroded, and sulfur oxidation is included in the gas released to the atmosphere. Things are included.
(2) 使用済樹脂の比放射能(Ci/g)は一般に雑固体
よりも高いため、除塵機から発生する粉塵の比放射能も
雑固体焼却の場合と比較して高くなり、除塵機の灰取出
部、灰ドラム等の表面線量率が高くなり被曝量がふえ
る。線量率(200mR/Hr以上)によっては、貯蔵庫へその
ままでは運搬できなくなるドラムが発生する。(2) Since the specific activity (Ci / g) of the used resin is generally higher than that of the coarse solids, the specific activity of the dust generated from the dust remover is also higher than that of the incinerator of the coarse solids. The surface dose rate of the ash extraction part, ash drum, etc. becomes high and the exposure dose increases. Depending on the dose rate (200 mR / Hr or more), some drums cannot be transported to storage as they are.
本発明の目的は上述した不具合を解消して、セラミック
フィルタの表面に特定成分の被覆層を設けることにより
燃焼排ガス中の硫黄酸化物を除去するとともに、除塵機
より発生する粉塵の比放射能を低減させ、使用済樹脂を
安全に焼却処理できる放射性廃棄物の処理方法を提供し
ようとするものである。The object of the present invention is to eliminate the above-mentioned problems and to remove the sulfur oxides in the combustion exhaust gas by providing a coating layer of a specific component on the surface of the ceramic filter, and to increase the specific activity of the dust generated by the dust remover. An object of the present invention is to provide a method for treating radioactive waste that can reduce the amount of used resin and safely incinerate it.
(問題点を解決するための手段) 本発明は放射性廃棄物の処理方法は、放射性物質取扱施
設において発生する使用済樹脂の焼却処理により発生す
る排ガスを、多孔質で有底円筒状のセラミックフィルタ
エレメントをその内部に配設した高温用除塵機を通過さ
せて処理する際に、前記セラミックフィルタエレメント
の排ガス導入側表面に、酸化カルシウム、酸化第二鉄、
酸化亜鉛、酸化第一銅のいずれか1種又は2種以上から
なり、粉粒状でその平均粒子径が100μm以下のろ過助
材からなる被覆層を設け、前記排ガス中の硫黄酸化物を
前記被覆層により捕集し、高温用除塵機から排出される
ろ過後の排ガス中の硫黄酸化物濃度を低減するととも
に、前記被覆層のろ過助材が化学量論的に等しい硫黄と
反応し、脱硫効率が急激に低下する前に逆洗して、捕集
した放射性粒子とろ過助材とを一緒に脱落させ高温用除
塵機より排出することにより、比放射能の低い除塵灰を
得ることを特徴とするものである。(Means for Solving Problems) The present invention is directed to a method for treating radioactive waste, in which exhaust gas generated by incineration of used resin generated in a radioactive substance handling facility is a porous, bottomed cylindrical ceramic filter. When the element is processed by passing through a high temperature dust remover disposed inside the element, on the exhaust gas introduction side surface of the ceramic filter element, calcium oxide, ferric oxide,
A coating layer made of any one or more of zinc oxide and cuprous oxide, which is a powder and has a filter aid having an average particle diameter of 100 μm or less is provided, and the sulfur oxide in the exhaust gas is coated with the coating layer. The concentration of sulfur oxides in the exhaust gas after filtration, which is collected by the bed and discharged from the high-temperature dust remover, is reduced, and the filter aid of the coating layer reacts with the stoichiometrically equal sulfur, resulting in desulfurization efficiency. Backwash before it drops sharply, the collected radioactive particles and the filter aid are dropped together and discharged from the high temperature dust remover to obtain dust ash with low specific activity. To do.
(作 用) 炭酸カルシウム等の無機物を用いた排ガスの脱硫は一般
に50%程度の効率しか得られない。その理由は、一般に
重油、石炭等の燃焼により発生する硫黄酸化物は90%以
上が二酸化イオウ(SO2)であり、三酸化イオウ(SO3)
は10%以下である一方、SO3は反応性に富み脱硫されや
すいが、SO2はSO3よりも反応性が弱いため脱硫されにく
いためである。従ってあまり脱硫効率が得られないため
実用化されていない。(Operation) Desulfurization of exhaust gas using inorganic substances such as calcium carbonate generally yields only about 50% efficiency. The reason is that, in general, sulfur dioxide (SO 2 ) accounts for 90% or more of sulfur oxides generated by combustion of heavy oil, coal, etc., and sulfur trioxide (SO 3 )
Is less than 10%, while SO 3 is highly reactive and easily desulfurized, but SO 2 is less reactive than SO 3 and is less desulfurized. Therefore, the desulfurization efficiency cannot be obtained so much, so that it has not been put to practical use.
一方、使用済樹脂中の硫黄は−SO3H(スルホン基)の形
で存在しているため、生成した硫黄酸化物のうち主成分
がSO3であり、脱硫のしやすい酸化物形態で存在する。
したがって、50%以上の脱硫効果が得られる。On the other hand, since sulfur in the used resin exists in the form of -SO 3 H (sulfone group), the main component of the generated sulfur oxide is SO 3 , and it exists in an oxide form that is easily desulfurized. To do.
Therefore, a desulfurization effect of 50% or more can be obtained.
使用済樹脂により発生する灰(クラッド)はそのほとん
どが除塵機へ移行し捕集されるが、その発生割合は樹脂
の1〜5%である。Most of the ash (clad) generated by the used resin moves to the dust remover and is collected, but the generation rate is 1 to 5% of the resin.
これに対し樹脂中の硫黄分は10〜15%であるためこれを
脱硫するに必要なろ過助材の量は樹脂の15〜20%程が化
学量論的に必要である。したがって、これら捕集粉塵を
ろ過助材と共に排出した場合の比放射能はろ過助材を用
いない場合と比較し1〜5/15〜20=1/20〜1/3に低減す
ることができる。On the other hand, since the sulfur content in the resin is 10 to 15%, about 15 to 20% of the resin is stoichiometrically required for desulfurizing the sulfur. Therefore, the specific activity when these collected dusts are discharged together with the filter aid can be reduced to 1 to 5/15 to 20 = 1/20 to 1/3 as compared with the case where the filter aid is not used. .
第1図は本発明で使用する高温用除塵機の一実施例を示
す斜視断面図である。本実施例において、除塵機1は下
部に排ガス導入口3および燃焼バーナ4、上側部に排ガ
ス導出口5さらに上部に逆洗用の空気導入口6を有する
耐火物7で内張りした缶体内に約100本の有底円筒状の
セラミックフィルタエレメント8を懸架した構成となっ
ている。放射性廃棄物を焼却する焼却炉からの燃焼排ガ
スは排ガス導入口3から除塵機1中に供給され、セラミ
ックフィルタエレメント8を外面より通過して放射能で
汚染されたダスト等がろ過された清浄な排ガスは排ガス
導出口5から機外に排出される構造となっており、燃焼
排ガスの除塵、ダスト未燃分の再燃焼、未燃ガスの完全
燃焼の各機能を有している。FIG. 1 is a perspective sectional view showing an embodiment of a high temperature dust remover used in the present invention. In the present embodiment, the dust remover 1 is provided with a flue gas inlet 3 and a combustion burner 4 in the lower portion, an exhaust gas outlet 5 in the upper portion, and an air inlet 6 for backwashing in the upper portion. It has a structure in which 100 cylindrical ceramic filter elements 8 having a bottom are suspended. Combustion exhaust gas from an incinerator that incinerates radioactive waste is supplied into the dust remover 1 through the exhaust gas inlet 3, passes through the ceramic filter element 8 from the outer surface, and is filtered to remove dust and the like contaminated with radioactivity. Exhaust gas is discharged from the exhaust gas outlet 5 to the outside of the machine, and has the functions of dust removal of combustion exhaust gas, recombustion of unburned dust, and complete combustion of unburned gas.
第2図は本発明で使用するフィルタエレメント8の一実
施例を示す線図である。本実施例のフィルタエレメント
8は、好ましくは例えばSiC等の微細粒子等を無機質結
合剤で結合した多孔体のセラミックスよりなり、長さ10
00mmまたは1500mm、直径60mm、肉圧10mm程度の有底円筒
形であり、排ガスは筒状体の外周から内部へ通り抜ける
構造となっている。FIG. 2 is a diagram showing an embodiment of the filter element 8 used in the present invention. The filter element 8 of this embodiment is preferably made of porous ceramics in which fine particles such as SiC are bound by an inorganic binder and has a length of 10
It has a bottomed cylindrical shape with a diameter of 00 mm or 1500 mm, a diameter of 60 mm, and a wall pressure of about 10 mm, and has a structure in which exhaust gas passes from the outer periphery of the tubular body to the inside.
第3図は、本発明で使用するフィルタエレメント8の一
実施例である。本例では、フィルタエレメント8の外表
面全体に酸化カルシウム(CaO)、酸化第二鉄(Fe
2O3)、酸化亜鉛(ZnO)、酸化第一銅(CuO)のいずれ
か又はこれらの複数からなる粉粒状のろ過助材からなる
被覆層11を設けている。このときCaO,Fe2O3,ZnO,CuOか
らなる粉粒状のろ過助材の平均粒子径は100μm以下と
する必要があり、好ましくは10μm〜50μmが好まし
い。その理由は被覆層11の平均粒子径が100μm以上だ
と効果が小さく、10μm以下だと初期の圧力損失が大き
くなりすぎるためである。第3図に示したフィルタエレ
メント8においては、硫黄を含有する放射性廃棄物中に
予じめ硫黄に対して化学量論的に過剰量となるだけのろ
過助材が被覆してあるので、排ガス中の硫黄酸化物は、
CaSO4,Fe2(SO4)3,ZnSO4,CuSO4となり被覆層上で好適
に捕集することができる。FIG. 3 shows an embodiment of the filter element 8 used in the present invention. In this example, calcium oxide (CaO) and ferric oxide (Fe) are formed on the entire outer surface of the filter element 8.
2 O 3 ), zinc oxide (ZnO), cuprous oxide (CuO), or a coating layer 11 made of a powdery or granular filter aid made of a plurality thereof. At this time, the average particle diameter of the powdery particulate filter aid made of CaO, Fe 2 O 3 , ZnO, and CuO must be 100 μm or less, and preferably 10 μm to 50 μm. The reason is that if the average particle size of the coating layer 11 is 100 μm or more, the effect is small, and if it is 10 μm or less, the initial pressure loss becomes too large. In the filter element 8 shown in FIG. 3, since the radioactive waste containing sulfur is coated with a filter aid that is stoichiometrically excessive with respect to the amount of sulfur, the exhaust gas is exhausted. The sulfur oxide in
It becomes CaSO 4 , Fe 2 (SO 4 ) 3 , ZnSO 4 , CuSO 4 and can be favorably collected on the coating layer.
被覆層のろ過助材が化学量論的に等しい硫黄と反応し、
脱硫効率が急激に低下する前に逆洗を行い、捕集した放
射性粒子とろ過助材を一緒に除塵機より排出することに
より粉塵の比放射能を低減することができる。The filter aid in the coating reacts with the stoichiometrically equal sulfur,
It is possible to reduce the specific activity of dust by performing backwashing before the desulfurization efficiency sharply decreases and discharging the collected radioactive particles and the filter aid together from the dust remover.
逆洗を行うには、第1図に示す高温用除塵機において、
まず例えば排ガス導出口5を閉鎖し空気導入口6に遮断
弁を介して空気タンク(図示せず)に接続した状態で、
排ガス導入口3に真空ポンプ等を接続して除塵機1内を
−1000mmAq程度の負圧にする。この状態で遮断弁を開き
フィルタエレメント8の筒状体の内周側から外周側へ圧
縮空気を瞬間的に流すことにより、フィルタエレメント
表面の被覆層11が剥離され落下して再生処理ができる。To perform backwashing, in the high temperature dust remover shown in FIG.
First, for example, in a state where the exhaust gas outlet port 5 is closed and the air inlet port 6 is connected to an air tank (not shown) via a shutoff valve,
A vacuum pump or the like is connected to the exhaust gas inlet 3 to make the inside of the dust remover 1 a negative pressure of about -1000 mmAq. In this state, the shut-off valve is opened, and compressed air is instantaneously flown from the inner peripheral side to the outer peripheral side of the cylindrical body of the filter element 8, whereby the coating layer 11 on the surface of the filter element is peeled off and dropped, and the regeneration treatment can be performed.
実施例1 硫黄を7.5%含む使用済樹脂(カチオン樹脂/アニオン
樹脂=1/1)を雑固体焼却炉内で焼却して、第1表に示
すセラミックフィルタエレメントをそれぞれ装着した第
1図に示す除塵機を用いてろ過除塵を行い、脱硫効率を
測定するとともに、脱硫効率が低下する前に逆洗を行
い、逆洗灰を200ドラムに充填した時の灰ドラム表面
線量率を測定した。結果を第1表に示す。Example 1 A used resin (cationic resin / anionic resin = 1/1) containing 7.5% of sulfur was incinerated in a solid-state incinerator, and the ceramic filter elements shown in Table 1 are attached to each and shown in FIG. The desulfurization efficiency was measured using a dust remover, the desulfurization efficiency was measured, and backwash was performed before the desulfurization efficiency decreased, and the ash drum surface dose rate when the backwash ash was filled in 200 drums was measured. The results are shown in Table 1.
第1表から明らかなように、フィルタエレメントに何の
被覆層も設けない従来例では脱硫はほとんどされず、灰
ドラム表面線量率も運搬基準値である200mR/Hrを大きく
上まわっているのに比べて、CaO,Fe2O3,CuO,ZnO等のい
ずれか一種以上よりなる被覆層を設けた場合には90%以
上に脱硫効果が得られ、逆洗灰を充填した灰ドラム表面
線量率も200mR/Hr以下にすることができた。 As is clear from Table 1, desulfurization is hardly performed and the ash drum surface dose rate greatly exceeds the transport standard value of 200 mR / Hr in the conventional example in which no coating layer is provided on the filter element. In comparison, when a coating layer consisting of one or more of CaO, Fe 2 O 3 , CuO, ZnO, etc. was provided, a desulfurization effect was obtained at 90% or more, and the surface dose rate of the ash drum filled with backwash ash was obtained. Could be less than 200mR / Hr.
(発明の効果) 以上詳細に説明したところから明らかなように、本発明
の放射性廃棄物の処理方法によれば、排ガス導入側表面
に脱硫剤よりなる被覆層を有するセラミックフィルタエ
レメントを使用して放射性排ガスをろ過することによ
り、使用済樹脂焼却時に発生する硫黄酸化物を除去する
ことができるため、大気汚染を低減することができる。
また、硫黄酸化物による焼却設備の腐食を低減すること
ができるとともに、逆洗により取出す灰の比放射能を低
減できるため、除塵機、灰ドラムからの放射線被曝量を
低減することができる。(Effect of the Invention) As is clear from the above description, according to the method for treating radioactive waste of the present invention, the ceramic filter element having the coating layer made of the desulfurizing agent on the surface of the exhaust gas introduction side is used. By filtering the radioactive exhaust gas, the sulfur oxides generated during the incineration of the used resin can be removed, so that the air pollution can be reduced.
Further, it is possible to reduce the corrosion of the incineration equipment due to the sulfur oxides and to reduce the specific activity of the ash taken out by the backwash, so that the radiation exposure dose from the dust remover and the ash drum can be reduced.
第1図は本発明で使用する高温用除塵機の一実施例を示
す斜視断面図、 第2図は本発明で使用するフィルタエレメントの一実施
例を示す線図、 第3図は本発明で使用するフィルタエレメントの一実施
例を部分拡大して示す断面図である。 1……除塵機、2……灰取出口 3……排ガス導入口、4……二次燃焼バーナ 5……排ガス導出口、6……逆洗用空気導入口 7……耐火物、8……フィルタエレメント 11……被覆層FIG. 1 is a perspective sectional view showing an embodiment of a high temperature dust remover used in the present invention, FIG. 2 is a diagram showing an embodiment of a filter element used in the present invention, and FIG. It is sectional drawing which expands and shows one Example of the filter element used. 1 ... Dust remover, 2 ... Ash removal port 3 ... Exhaust gas inlet port, 4 ... Secondary combustion burner 5 ... Exhaust gas outlet port, 6 ... Backwash air inlet port, 7 ... Refractory material, 8 ... … Filter element 11… Coating layer
Claims (2)
済樹脂の焼却処理により発生する排ガスを、多孔質で有
底円筒状のセラミックフィルタエレメントをその内部に
配設した高温用除塵機を通過させて処理する際に、前記
セラミックフィルタエレメントの排ガス導入側表面に、
酸化カルシウム、酸化第二鉄、酸化亜鉛、酸化第一銅の
いずれか1種又は2種以上からなり、粉粒状でその平均
粒子径が100μm以下のろ過助材からなる被覆層を設
け、前記排ガス中の硫黄酸化物を前記被覆層により捕集
し、高温用除塵機から排出されるろ過後の排ガス中の硫
黄酸化物濃度を低減するとともに、前記被覆層のろ過助
材が化学量論的に等しい硫黄と反応し、脱硫効率が急激
に低下する前に逆洗して、捕集した放射性粒子とろ過助
材とを一緒に脱落させ高温用除塵機より排出することに
より、比放射能の低い除塵灰を得ることを特徴とする放
射性廃棄物の処理方法。1. Exhaust gas generated by incineration of used resin generated in a radioactive material handling facility is passed through a high temperature dust remover having a porous, bottomed cylindrical ceramic filter element disposed therein. During processing, on the exhaust gas introduction side surface of the ceramic filter element,
The exhaust gas is provided with a coating layer made of any one or more of calcium oxide, ferric oxide, zinc oxide, and cuprous oxide, which is in the form of powder and has an average particle diameter of 100 μm or less. Sulfur oxides in the collected by the coating layer, reducing the concentration of sulfur oxides in the exhaust gas after filtration discharged from the high temperature dust remover, the filter aid of the coating layer stoichiometrically Reacts with equal sulfur, backwashes before the desulfurization efficiency drops sharply, removes the collected radioactive particles and filter aid together, and discharges them from the high temperature dust remover, resulting in low specific activity A method for treating radioactive waste, characterized by obtaining dust ash.
る特許請求の範囲第1項記載の放射性廃棄物の処理方
法。2. The method for treating radioactive waste according to claim 1, wherein the temperature of the high-temperature dust remover is 500 ° C. or higher.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61264893A JPH077109B2 (en) | 1986-11-08 | 1986-11-08 | How to dispose of radioactive waste |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61264893A JPH077109B2 (en) | 1986-11-08 | 1986-11-08 | How to dispose of radioactive waste |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63120300A JPS63120300A (en) | 1988-05-24 |
| JPH077109B2 true JPH077109B2 (en) | 1995-01-30 |
Family
ID=17409689
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61264893A Expired - Lifetime JPH077109B2 (en) | 1986-11-08 | 1986-11-08 | How to dispose of radioactive waste |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH077109B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6368079B2 (en) * | 2013-10-01 | 2018-08-01 | 日本碍子株式会社 | Radioactive waste volume reduction treatment apparatus and volume reduction treatment method |
| CN113041713B (en) * | 2021-03-11 | 2022-11-15 | 太原理工大学 | A method for dewatering coal slime with metal oxide nanoparticles |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0230680B2 (en) * | 1983-05-18 | 1990-07-09 | Ngk Insulators Ltd | HOSHASEIHAIKIBUTSUNOSHORIHOHO |
| JPS60202714A (en) * | 1984-03-22 | 1985-10-14 | Matsushita Electric Ind Co Ltd | SOx removal filter |
-
1986
- 1986-11-08 JP JP61264893A patent/JPH077109B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63120300A (en) | 1988-05-24 |
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