JP6410058B2 - Ash processing equipment containing radioactive cesium oxide - Google Patents
Ash processing equipment containing radioactive cesium oxide Download PDFInfo
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- JP6410058B2 JP6410058B2 JP2016223990A JP2016223990A JP6410058B2 JP 6410058 B2 JP6410058 B2 JP 6410058B2 JP 2016223990 A JP2016223990 A JP 2016223990A JP 2016223990 A JP2016223990 A JP 2016223990A JP 6410058 B2 JP6410058 B2 JP 6410058B2
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- 230000002285 radioactive effect Effects 0.000 title claims description 47
- KOPBYBDAPCDYFK-UHFFFAOYSA-N caesium oxide Chemical compound [O-2].[Cs+].[Cs+] KOPBYBDAPCDYFK-UHFFFAOYSA-N 0.000 title claims description 20
- 229910001942 caesium oxide Inorganic materials 0.000 title claims description 20
- 239000000460 chlorine Substances 0.000 claims description 21
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 20
- 229910052801 chlorine Inorganic materials 0.000 claims description 20
- 239000011701 zinc Substances 0.000 claims description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- 239000002956 ash Substances 0.000 description 53
- 229910052792 caesium Inorganic materials 0.000 description 33
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 33
- 239000007789 gas Substances 0.000 description 33
- 238000002485 combustion reaction Methods 0.000 description 12
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 10
- 229910002091 carbon monoxide Inorganic materials 0.000 description 10
- 239000004568 cement Substances 0.000 description 10
- AIYUHDOJVYHVIT-UHFFFAOYSA-M caesium chloride Chemical compound [Cl-].[Cs+] AIYUHDOJVYHVIT-UHFFFAOYSA-M 0.000 description 9
- 239000010881 fly ash Substances 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 239000003575 carbonaceous material Substances 0.000 description 8
- 239000002994 raw material Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000000428 dust Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000012857 radioactive material Substances 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 2
- 229910001617 alkaline earth metal chloride Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001868 water Inorganic materials 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 1
- 239000003830 anthracite Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000010882 bottom ash Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000010849 combustible waste Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 150000002013 dioxins Chemical class 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- HWSZZLVAJGOAAY-UHFFFAOYSA-L lead(II) chloride Chemical compound Cl[Pb]Cl HWSZZLVAJGOAAY-UHFFFAOYSA-L 0.000 description 1
- 239000003949 liquefied natural gas Substances 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002901 radioactive waste Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004056 waste incineration Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
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Description
本発明は、放射性セシウムの酸化物を含有する灰から放射性セシウムを除去し、さらにこの灰を有効利用しうる装置に関するものである。 The present invention relates to an apparatus capable of removing radioactive cesium from ash containing an oxide of radioactive cesium and further making effective use of this ash.
原子力発電所等の放射性物質を取扱う施設から排出される廃棄物のうち可燃性のものは焼却処理されるが、その焼却の際に発生する焼却灰には放射性物質が含まれており、そのなかで放射性セシウムは半減期が134Csで約2年、137Csで約30年と長いので、その保管には細心の注意を払う必要がある。特に、最近では福島県の原子力発電所の事故により多量の放射性物質が放出されて広範囲にわたって汚染を引起し、その汚染地域から出される可燃物の焼却灰の処理も問題になっている。 Combustible waste discharged from facilities that handle radioactive materials such as nuclear power plants is incinerated, and the incineration ash generated during the incineration contains radioactive materials. Since radioactive cesium has a long half-life of 134 Cs for about 2 years and 137 Cs for about 30 years, it must be carefully stored. In particular, recently, a large amount of radioactive material has been released due to an accident at a nuclear power plant in Fukushima Prefecture, causing pollution over a wide area, and the treatment of incinerated ash from combustible materials emitted from the contaminated area has also become a problem.
そこで、環境省では、放射性セシウム濃度が8,000Bq/kgを超え100,000Bq/kg以下の焼却灰については、セメントを加えて固化物とし、セメント固化物の周囲を覆って埋立処分する指針を示している(非特許文献1)。 Therefore, the Ministry of the Environment has a guideline for incineration ash with radioactive cesium concentration exceeding 8,000 Bq / kg and 100,000 Bq / kg or less to make solidified by adding cement and covering the periphery of the cement solidified by landfill. (Non-Patent Document 1).
また、放射性廃棄物の焼却灰をセメントで固化する際に、焼却処理によって生じた塩化鉛等の重金属塩化物を水への溶解性が低い状態に変換する方法も開示されている(特許文献1)。この変換には、アルカリ金属水酸化物やアルカリ土類金属水酸化物などが用いられている。 Moreover, when solidifying the incinerated ash of radioactive waste with cement, a method of converting heavy metal chlorides such as lead chloride produced by incineration to a state having low solubility in water is also disclosed (Patent Document 1). ). For this conversion, an alkali metal hydroxide, an alkaline earth metal hydroxide, or the like is used.
焼却灰のセメント固化物には亀裂が入っていることがあり、その場合、雨水が浸透するとこの亀裂から放射性セシウムが溶出してくる。そこで、従来の埋立方法では、埋立処分場の構造を変えて、隔壁層を設けたり、コンクリート容器に入れたり、処分場からの廃水を処理する方法などが挙げられている。しかしながら、放射性セシウムは漏出しないよう細心の注意を払う必要があり、これらの方法でも、運搬中のトラブルや地震などによる処分場の地割れや廃水処理設備のトラブルなどの不測の事態が起これば放射性セシウムが漏出する懸念がある。 Incinerated ash cement solids may have cracks. In such a case, when rainwater penetrates, radioactive cesium is eluted from the cracks. Therefore, conventional landfill methods include methods of changing the structure of the landfill disposal site to provide a partition wall layer, putting it in a concrete container, or treating waste water from the disposal site. However, it is necessary to pay close attention to prevent radioactive cesium from leaking out. Even if these methods are used, if there is an unforeseen situation such as a trouble during transportation, a crack in the disposal site due to an earthquake, or a trouble in the wastewater treatment facility, it will be radioactive. There is concern that cesium may leak.
また、埋立ではなく、セメント原料として利用しようとする場合、放射性セシウムが残留していて、有効利用の基準であるクリアランスレベルの100Bq/kgを超えているため有効利用できなかった。 In addition, when trying to use it as a cement raw material instead of landfill, it could not be used effectively because radioactive cesium remained and exceeded the clearance level of 100 Bq / kg which is the standard for effective use.
本発明の目的は、放射性セシウムの酸化物を含有する灰から放射性セシウムを効率よく除去して灰をセメント原料などに有効利用できる装置を提供することにある。 An object of the present invention is to provide an apparatus capable of efficiently removing radioactive cesium from ash containing an oxide of radioactive cesium and effectively using the ash as a cement raw material.
本発明者は、上記課題を解決するべく鋭意検討の結果、灰に含まれている放射性セシウムは主に酸化物等の形態で存在していることを見出した。そして、これを塩素の存在下で還元ガス雰囲気で加熱することによって、放射性セシウムを塩化物の形態に変えて揮発させ飛灰側に濃縮することができ、残った灰は放射性セシウムをほとんど含有しない無害なものになることを見出した。 As a result of intensive studies to solve the above-mentioned problems, the present inventor has found that radioactive cesium contained in ash is present mainly in the form of an oxide or the like. And by heating it in a reducing gas atmosphere in the presence of chlorine, radioactive cesium can be converted into a chloride form to volatilize and concentrate on the fly ash side, and the remaining ash contains almost no radioactive cesium. I found out that it would be harmless.
そして、さらに、炭材を炉に投入して還元ガス雰囲気を形成し、放射性セシウムを除去した後、残存している炭材を燃焼させて除去することにより、この灰をセメント原料などに有効利用できることを見出した。 Furthermore, the ash is effectively used as a cement raw material, etc. by putting the carbonaceous material into the furnace to form a reducing gas atmosphere and removing radioactive cesium, and then burning and removing the remaining carbonaceous material. I found out that I can do it.
本発明は、これらの知見に基いてなされたものであり、放射性セシウムの酸化物を含有する灰の投入口と、炉内ガスの排気口と、灰の排出口と、塩素源の投入口を有し、放射性セシウムの酸化物を含有する灰を前記灰中に存在する塩素成分あるいは添加した塩素源を用いて、800〜1100℃の還元ガス雰囲気下で還元して放射性セシウムを塩化セシウムとして揮発させる還元揮発炉を備えたことを特徴とする放射性セシウムの酸化物を含有する灰の処理装置を提供するものである。 The present invention has been made on the basis of these findings, and includes an ash inlet containing radioactive cesium oxide, an in-furnace gas outlet, an ash outlet, and a chlorine source inlet. The ash containing radioactive cesium oxide is reduced in a reducing gas atmosphere at 800 to 1100 ° C. using the chlorine component present in the ash or the added chlorine source, and the radioactive cesium is volatilized as cesium chloride. The present invention provides an apparatus for treating ash containing an oxide of radioactive cesium, comprising a reduction volatilization furnace.
本発明により、放射性セシウムの酸化物を含有する灰から放射性セシウムをほとんど含有しない灰に変えることができ、その際発生する飛灰のみを埋立処理すればよいので埋立量を大幅に減少させることができる。また、放射性セシウムを除去した灰はセメント原料などに有効利用することができる。 According to the present invention, the ash containing the radioactive cesium oxide can be changed to the ash containing almost no radioactive cesium, and only the fly ash generated at that time has to be landfilled, so that the amount of landfill can be greatly reduced. it can. Moreover, the ash from which radioactive cesium has been removed can be effectively used as a cement raw material.
本発明の装置が適用される灰は、放射性セシウムの酸化物を含有する灰であり、例えば、放射性セシウムを含有する可燃物を焼却した際に発生する焼却灰やその主灰を溶融してスラグ化する際に発生する溶融飛灰などである。放射性セシウムを含有する可燃物を焼却した際に発生する焼却灰には、焼却炉の炉底に溜まる炉底灰である主灰と、燃焼排ガスに含まれてバグフィルター等の集塵機で捕集される飛灰がある。また、この主灰を溶融炉で加熱溶融してスラグ化する際に発生してバグフィルター等の集塵機で捕集される溶融飛灰もある。これら飛灰のセシウムの含有量は通常0.1〜10ppm程度であり、そのうち、放射性セシウムの含有量は、放射能濃度により異なるが、初期の灰の放射線濃度を134Csと137Csが等しく、たとえば、それぞれ500Bq/kg(すなわち、合計で1,000Bq/kg)とすると、134Csは約10pg/kg、137Csは約155pg/kgと極微量である。 The ash to which the apparatus of the present invention is applied is an ash containing an oxide of radioactive cesium. For example, incineration ash generated when incinerated combustibles containing radioactive cesium and its main ash are melted to form slag. For example, molten fly ash generated during the process. The incineration ash generated when incineration of combustible materials containing radioactive cesium is collected by the main ash that is the bottom ash collected at the bottom of the incinerator and collected by a dust collector such as a bag filter that is contained in the combustion exhaust gas. There is fly ash. There is also a molten fly ash that is generated when the main ash is heated and melted in a melting furnace to be slag and collected by a dust collector such as a bag filter. The cesium content of these fly ash is usually about 0.1 to 10 ppm, of which the radioactive cesium content varies depending on the radioactivity concentration, but the initial ash radiation concentration is equal to 134 Cs and 137 Cs, For example, if each of them is 500 Bq / kg (that is, 1,000 Bq / kg in total), 134 Cs is about 10 pg / kg and 137 Cs is about 155 pg / kg, which is a very small amount.
本発明の装置は、放射性セシウムの酸化物を含有する灰を還元して揮発させるための還元揮発炉から構成される。 The apparatus of the present invention comprises a reduction volatilization furnace for reducing and volatilizing ash containing radioactive cesium oxide.
還元揮発炉では、還元ガス雰囲気下で炭材を添加して灰を加熱し、灰中の酸化セシウムを還元し、灰中に存在する塩素成分あるいは添加した塩素源を用いて塩化セシウムとする。また、本来灰中に存在している塩化セシウムについては、還元ガス雰囲気にすることにより酸化を抑制することができる。このようにして、放射性セシウムの酸化物を塩化セシウムとして揮発させ、次工程の燃焼炉において灰中の炭素分を燃焼除去する。 In a reduction volatilization furnace, carbonaceous material is added in a reducing gas atmosphere to heat the ash, cesium oxide in the ash is reduced, and cesium chloride is obtained using a chlorine component present in the ash or an added chlorine source. Moreover, about cesium chloride which originally exists in ash, oxidation can be suppressed by making it a reducing gas atmosphere. In this way, the radioactive cesium oxide is volatilized as cesium chloride, and the carbon content in the ash is burned and removed in the combustion furnace of the next step.
塩素は、加熱時に酸化セシウムを塩化セシウムの形態に変えるものであり、多種多様のものを用いることができる。放射性セシウムの酸化物を含有する灰中には、0.4〜2重量%の塩素成分を含むことが多く、塩素成分の含有量が0.4重量%未満の場合には塩素源を添加する必要がある。 Chlorine changes cesium oxide into a form of cesium chloride during heating, and a wide variety can be used. The ash containing radioactive cesium oxide often contains 0.4 to 2% by weight of chlorine component, and if the chlorine component content is less than 0.4% by weight, a chlorine source is added. There is a need.
塩素源として、例示すれば、塩化ビニル樹脂、アルカリ金属の塩化物、アルカリ土類金属の塩化物等が挙げられる。アルカリ金属の塩化物として、塩化ナトリウム、塩化カリウムなどがあり、アルカリ土類金属の塩化物として、塩化カルシウム、塩化マグネシウムなどがある。 Examples of the chlorine source include vinyl chloride resins, alkali metal chlorides, alkaline earth metal chlorides, and the like. Examples of the alkali metal chloride include sodium chloride and potassium chloride, and examples of the alkaline earth metal chloride include calcium chloride and magnesium chloride.
塩素の含有量としては、放射性セシウムの酸化物を含有する灰に含まれる鉛の当量と亜鉛の当量との合計以上であることが好ましい。これは、鉛および亜鉛は塩化し易く、しかもセシウムよりも揮発し易い元素であるためである。なお、鉛および亜鉛の各当量は、鉛および亜鉛の各物質量(モル数)の2倍で計算することができ、灰中に塩素成分が含まれていれば、これも塩素の含有量として含んで計算してもよい。 The chlorine content is preferably at least the sum of the equivalents of lead and zinc contained in the ash containing the radioactive cesium oxide. This is because lead and zinc are easily chlorinated and more volatile than cesium. In addition, each equivalent of lead and zinc can be calculated by double the amount of each substance (number of moles) of lead and zinc. If chlorine component is contained in ash, this is also calculated as chlorine content. You may calculate including.
灰を加熱する炉は、粉、粒体を1000℃程度に加熱できる炉であればよいが、密閉型のものであり、攪拌機構が付いているものが好ましい。その外、灰や塩素源、炭材等の投入口、炉内ガスの排気口、放射性セシウムを除去した灰の排出口などが必要である。本発明を適用できる炉を例示すれば、ロータリーキルン、ストーカ炉等を挙げることができる。 The furnace for heating the ash may be any furnace that can heat the powder and granules to about 1000 ° C., but is preferably a closed type and equipped with a stirring mechanism. In addition, an inlet for ash and chlorine sources, charcoal, etc., an exhaust port for furnace gas, and an ash outlet from which radioactive cesium has been removed are necessary. Examples of furnaces to which the present invention can be applied include rotary kilns and stoker furnaces.
還元揮発炉において、炉内を還元ガス雰囲気にするために、炉内ガスは、一酸化炭素ガス、二酸化炭素ガス、水素ガス、窒素ガス、水および1体積%未満の酸素ガスから構成されることが好ましい。 In a reduction volatile furnace, in order to make the inside of the furnace a reducing gas atmosphere, the furnace gas is composed of carbon monoxide gas, carbon dioxide gas, hydrogen gas, nitrogen gas, water and oxygen gas of less than 1% by volume. Is preferred.
一酸化炭素ガスを還元ガス雰囲気とする場合には、炉内に炭材を投入して、これを不完全燃焼、あるいは液体燃料や気体燃料を不完全燃焼させればよい。 When carbon monoxide gas is used as a reducing gas atmosphere, a carbon material may be put into the furnace and incompletely combusted, or liquid fuel or gaseous fuel may be incompletely combusted.
炭材としては、コークス、無煙炭、黒鉛などを用いることができる。液体燃料としては、重油、廃油などを用いることができ、気体燃料としては、液化天然ガス、液化石油ガスなどを用いることができる。 As the carbon material, coke, anthracite, graphite, or the like can be used. As the liquid fuel, heavy oil, waste oil, or the like can be used, and as the gaseous fuel, liquefied natural gas, liquefied petroleum gas, or the like can be used.
一酸化炭素ガスの濃度としては、5〜40体積%程度であることが好ましく、特に20〜30体積%程度であることがより好ましい。さらに、一酸化炭素ガスと二酸化炭素ガスとの濃度比(CO/CO2)は、0.1〜100程度であることが好ましく、特に0.5〜20程度であることがより好ましい。 The concentration of the carbon monoxide gas is preferably about 5 to 40% by volume, and more preferably about 20 to 30% by volume. Furthermore, the concentration ratio (CO / CO 2 ) between carbon monoxide gas and carbon dioxide gas is preferably about 0.1 to 100, and more preferably about 0.5 to 20.
一酸化炭素ガスの濃度が5体積%未満の場合、酸化性が強まるため、セシウムの塩化が進行しなくなる。一方、一酸化炭素ガスの濃度が40体積%を超えた場合ではセシウムが塩化する効果はほとんど変わらない。 When the concentration of the carbon monoxide gas is less than 5% by volume, the oxidization is strengthened, so that cesium chlorination does not proceed. On the other hand, when the concentration of carbon monoxide gas exceeds 40% by volume, the effect of cesium chloride is hardly changed.
また、一酸化炭素ガスと二酸化炭素ガスとの濃度比(CO/CO2)が0.1未満の場合、酸化性が強まるため、セシウムの塩化が進行しなくなる。一方、一酸化炭素ガスと二酸化炭素ガスとの濃度比(CO/CO2)が100を超えた場合ではセシウムが塩化する効果はほとんど変わらない。 Further, when the concentration ratio (CO / CO 2 ) between the carbon monoxide gas and the carbon dioxide gas is less than 0.1, the oxidization becomes stronger, so that cesium chlorination does not proceed. On the other hand, when the concentration ratio (CO / CO 2 ) between carbon monoxide gas and carbon dioxide gas exceeds 100, the effect of cesium chloride is hardly changed.
還元揮発炉の炉内は、放射性セシウムの酸化物を還元して塩素と反応させて塩化セシウムを形成させ、これを揮発させるために700℃以上、800〜1100℃程度とすることが好ましい。 The inside of the reduction volatilization furnace is preferably set to 700 ° C. or more and about 800 to 1100 ° C. in order to reduce the radioactive cesium oxide to react with chlorine to form cesium chloride and volatilize it.
揮発した塩化セシウムは、炉内に供給されるガス、例えば加熱のためのバーナーから供給される燃焼ガスによって炉外に排出され、燃焼炉から排出されたガスとともに混合され、燃焼炉において空気を吹き込むことによってガス中の一酸化炭素と水素を燃焼させる。 Volatilized cesium chloride is discharged out of the furnace by a gas supplied into the furnace, for example, a combustion gas supplied from a burner for heating, mixed with the gas discharged from the combustion furnace, and air is blown into the combustion furnace. By burning carbon monoxide and hydrogen in the gas.
排出されたガス中には、ダイオキシン類が含まれることがあるため、排ガスは燃焼炉内で、必要に応じてバーナーを用いて滞留時間を2秒以上確保した上で、850℃以上に加熱し、約200℃まで冷却した後、飛灰とともに集塵機で捕集される。集塵機には煙道の煤塵を捕集するものなどを用いることができ、例えばバグフィルターを利用できる。 Since the exhausted gas may contain dioxins, the exhaust gas is heated to 850 ° C. or higher in a combustion furnace with a residence time of 2 seconds or longer if necessary using a burner. After cooling to about 200 ° C., it is collected by a dust collector together with fly ash. As the dust collector, one that collects dust from the flue can be used, and for example, a bug filter can be used.
こうして、放射性セシウムを除去した灰は、還元ガス雰囲気を、炭材を用いて形成した場合には、炭材が残存している可能性がある。そこで、この残存している炭材がその後の灰の有効利用を阻害する場合にはこれを予め除去しておく必要がある。例えば灰の熱しゃく減量が5重量%以上の場合には、残存する炭素分を燃焼させて除去しておくことが好ましい。ここで、灰の熱しゃく減量とは、600℃で3時間強熱することにより、ごみ焼却残渣中に残っている未燃分の重量%を表す値で、熱しゃく減量が小さいほど良好な燃焼ができたことになる。 Thus, in the ash from which radioactive cesium has been removed, when a reducing gas atmosphere is formed using a carbon material, the carbon material may remain. Therefore, when the remaining carbon material hinders the subsequent effective use of ash, it is necessary to remove it beforehand. For example, when the heat loss of ash is 5% by weight or more, it is preferable to burn away the remaining carbon. Here, the heat loss of ash is a value that represents the weight percent of unburned residue remaining in the waste incineration residue when ignited at 600 ° C. for 3 hours. The smaller the heat loss, the better the combustion. It was possible.
燃焼炉は、前記の還元揮発炉とは別の炉で行うのがよい。両炉は別体であってもよく、一つの炉を2室に仕切った形態のものでもよい。燃焼は炭素分を充分に燃焼させるよう酸素を供給して行う。この酸素の供給は空気の吹込みで行うことができる。 The combustion furnace is preferably performed in a furnace different from the above reduction volatile furnace. Both furnaces may be separate bodies, or one furnace may be divided into two chambers. Combustion is performed by supplying oxygen so that the carbon content is sufficiently combusted. This supply of oxygen can be performed by blowing air.
用いた灰の組成は、Si:10重量%、Al:9重量%、Ca:20重量%、Na:4重量%、K:1重量%、Cl:1重量%、Pb:0.1重量%、Zn:0.4重量%であり、放射性セシウムの濃度(134Csと137Csの合計)は10,000Bq/kgである。 The composition of the ash used was Si: 10% by weight, Al: 9% by weight, Ca: 20% by weight, Na: 4% by weight, K: 1% by weight, Cl: 1% by weight, Pb: 0.1% by weight. Zn: 0.4% by weight, and the concentration of radioactive cesium (total of 134 Cs and 137 Cs) is 10,000 Bq / kg.
炉には、図1に示すものを用いた。この炉は、二段式のロータリーキルンで構成され、還元揮発炉の左端の投入口から灰を1kg/hr、コークスを0.03kg/hr、CaCl2を0.01kg/hrで炉内に連続投入した。還元揮発炉の右端のバーナーから火炎を吹込んで還元ガス雰囲気で加熱した。この雰囲気でのCO濃度は30体積%であり、炉内の温度は1000℃であった。灰の炉内での平均滞留時間は1時間であった。還元揮発炉のガス排気口から排出される排ガスは、燃焼炉から排出された排ガスと混合し、燃焼炉で一酸化炭素を燃焼させた後冷却し、煙道の途中に設けられたバグフィルター(図示されていない。)で集塵し、大気中に放出された。集塵した飛灰中の放射性セシウムの濃度は500,000Bq/kgであった。 The furnace shown in FIG. 1 was used. This furnace is composed of a two-stage rotary kiln and is continuously charged into the furnace at 1 kg / hr of ash, 0.03 kg / hr of coke, and 0.01 kg / hr of CaCl 2 from the leftmost inlet of the reduction volatilization furnace. did. A flame was blown from the burner at the right end of the reducing volatile furnace and heated in a reducing gas atmosphere. The CO concentration in this atmosphere was 30% by volume, and the temperature in the furnace was 1000 ° C. The average residence time of the ash in the furnace was 1 hour. The exhaust gas discharged from the gas exhaust port of the reduction volatile furnace is mixed with the exhaust gas discharged from the combustion furnace, burned with carbon monoxide in the combustion furnace, cooled, and a bag filter (in the middle of the flue) (It is not shown in the figure) and collected in the atmosphere. The concentration of radioactive cesium in the collected fly ash was 500,000 Bq / kg.
還元揮発炉から排出された灰は燃焼炉に移り、そこで、燃焼用空気とともに供給されるバーナーの火炎でさらに熱せられて残留する炭素分が燃焼除去された。この炉内の温度は1000℃であり、灰の炉内での平均滞留時間は1時間であった。 The ash discharged from the reduction volatilization furnace was transferred to the combustion furnace, where it was further heated by the burner flame supplied with the combustion air, and the remaining carbon was burned and removed. The temperature in the furnace was 1000 ° C., and the average residence time of the ash in the furnace was 1 hour.
得られた灰の放射性セシウムの濃度は50Bq/kgであり、そのままセメントの原料に用いても何ら問題がないことが分った。 The concentration of radioactive cesium in the obtained ash was 50 Bq / kg, and it was found that there was no problem even if it was used as a raw material for cement as it was.
本発明によれば、放射性セシウムの酸化物を含有する灰から放射性セシウムをほぼ完全に除去できるので埋立量をその際分離された飛灰のみ大幅に節減でき、かつ、放射性セシウムを除去された灰はセメント原料などに有効利用できるので、各種の放射性セシウムの酸化物を含有する灰の処理に利用できる。 According to the present invention, since radioactive cesium can be almost completely removed from ash containing radioactive cesium oxide, only the fly ash separated at that time can be significantly reduced, and the ash from which radioactive cesium has been removed can be saved. Can be effectively used as a raw material for cement and the like, and can be used for the treatment of ash containing various radioactive cesium oxides.
Claims (1)
前記放射性セシウムの酸化物を含有する灰を、前記放射性セシウムの酸化物を含有する灰中に存在する塩素成分あるいは添加した塩素源を用いて800〜1100℃の還元ガス雰囲気下で還元するとともに、前記還元揮発炉における塩素の含有量は、前記放射性セシウムの酸化物を含有する灰に含まれる鉛の当量と亜鉛の当量との合計以上とすることを特徴とする放射性セシウムの酸化物を含有する灰の処理装置。 It has a ash inlet containing radioactive cesium oxide, a furnace gas outlet, an ash outlet, and a chlorine source inlet to reduce ash containing radioactive cesium oxide. An apparatus for treating ash containing a radioactive cesium oxide, comprising a reduction volatilization furnace for volatilizing,
The ash containing the radioactive cesium oxide is reduced using a chlorine component present in the ash containing the radioactive cesium oxide or an added chlorine source in a reducing gas atmosphere of 800 to 1100 ° C. , The content of chlorine in the reducing volatile furnace contains a radioactive cesium oxide characterized by being equal to or more than the sum of the equivalent of lead and the equivalent of zinc contained in the ash containing the radioactive cesium oxide. Ash processing equipment.
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