JP3440246B2 - Waste residue treatment method - Google Patents

Waste residue treatment method

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Publication number
JP3440246B2
JP3440246B2 JP07962394A JP7962394A JP3440246B2 JP 3440246 B2 JP3440246 B2 JP 3440246B2 JP 07962394 A JP07962394 A JP 07962394A JP 7962394 A JP7962394 A JP 7962394A JP 3440246 B2 JP3440246 B2 JP 3440246B2
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JP
Japan
Prior art keywords
waste residue
metal
oxide
metal oxide
water
Prior art date
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JP07962394A
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Japanese (ja)
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JPH07256230A (en
Inventor
英明 宮出
Original Assignee
英明 宮出
堀口 直樹
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  • Processing Of Solid Wastes (AREA)
  • Treatment Of Sludge (AREA)
  • Fire-Extinguishing Compositions (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は金属ハロゲン化物を含有
する廃棄物残渣を安全に投棄または再利用可能な状態に
処理する方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for safely disposing of a metal halide-containing waste residue in a reusable state.

【0002】[0002]

【従来の技術】可燃廃棄物を焼却処分した際に生じる残
渣である焼却灰や、各種産業廃棄物を処理した際に生じ
る残渣である汚泥物には、有害重金属の酸化物、塩化物
などが含まれていることが多い。
2. Description of the Related Art Incinerated ash, which is a residue generated when combustible waste is incinerated, and sludge, which is a residue generated when processing various industrial wastes, contain harmful heavy metal oxides and chlorides. Often included.

【0003】例えば、一般廃棄物の内で紙、繊維製品、
プラスチックス、生ゴミ、各種合成化学物質などの可燃
廃棄物を清掃工場の焼却炉で焼却処分する際に、塩化ビ
ニル系プラスチックスなどから発生する有害な塩酸ガス
を捕捉するために酸化カルシウムなどを添加するが、こ
の酸化カルシウムは塩化カルシウムとなって焼却灰中に
残留する。
For example, paper, textiles,
When combustible wastes such as plastics, garbage and various synthetic chemical substances are incinerated in a cleaning plant incinerator, calcium oxide etc. are used to capture harmful hydrochloric acid gas generated from vinyl chloride plastics etc. Although added, this calcium oxide becomes calcium chloride and remains in the incineration ash.

【0004】しかし、この焼却灰には廃棄物の組成、焼
却温度などによる差異はあるが、本来的にかなりの高濃
度で含有されている水銀、鉛、カドミウム、亜鉛などの
有害な重金属が酸化物、塩化物などの化合物として存在
する。このような重金属の含有量が基準値以下であれば
そのまま埋立て地などに投棄することができるが、残渣
の単位重量当り含有量が微量であっても大量投棄による
総計は某大な量に達し、好ましくないことは明かであ
る。殊に、焼却炉の排気から分離回収したフライアッシ
ュには有害重金属が水に溶解しやすい塩化物として高濃
度に含有されており、そのまま投棄できないばかりか再
利用することもできない。
However, although there are differences in the incineration ash depending on the composition of the waste, the incineration temperature, etc., harmful heavy metals such as mercury, lead, cadmium and zinc, which are originally contained in a considerably high concentration, are oxidized. It exists as compounds such as compounds and chlorides. If the content of such heavy metals is below the standard value, it can be dumped as it is to landfills, etc., but even if the content of residue per unit weight is very small, the total amount due to mass dumping will be a certain large amount. It is clear that it has reached and is not desirable. In particular, the fly ash separated and collected from the exhaust gas of the incinerator contains a high concentration of harmful heavy metals as chlorides that are easily dissolved in water, and cannot be discarded as it is or reused.

【0005】一方、水に溶解しやすい前記重金属塩化物
のような金属ハロゲン化物を含有している焼却灰、汚泥
物を処理する方法、殊に再利用可能な状態に処理できる
方法として、セメントモルタルでコンクリート化するこ
と、高分子物質などの混和剤で固化すること、高熱を加
えてガラス化または焼結すること、が認められている。
On the other hand, cement mortar is used as a method for treating incineration ash and sludge containing a metal halide such as the above-mentioned heavy metal chloride which is easily dissolved in water, particularly as a method capable of treating it in a reusable state. It is recognized that it is made into concrete, solidified with an admixture such as a polymer substance, vitrified or sintered by applying high heat.

【0006】しかしながら、これらの方法によってブロ
ック、パネルなどの建築、構築材料を作りいわゆるリサ
イクル製品として提供した場合、これらに含有されてい
る重金属化合物が前記第一および第二の方法によって作
ったものにあっては雨水などにより容易に溶出して環境
を汚染する恐れが大きい、という問題がある。また、前
記第三の方法によるときは熱分解により有害な塩酸ガス
を発生して設備を腐食したり大気を汚染する、という問
題がある。
However, when building and building materials such as blocks and panels are produced by these methods and provided as so-called recycled products, the heavy metal compounds contained therein are those produced by the first and second methods. However, there is a problem that it is likely to be easily eluted by rainwater and pollute the environment. Further, the third method has a problem that harmful hydrochloric acid gas is generated by thermal decomposition to corrode equipment or pollute the atmosphere.

【0007】[0007]

【発明が解決しようとする課題】本発明が解決しようと
する課題は、廃棄物残渣を有害重金属が溶出しないよう
に処理する方法として認められている前記従来の方法で
は固化しても溶出を完全に防止できず環境汚染の問題が
残り、ガラス化または焼結を計ると設備を腐食し経済面
で著しく不利であるばかりか有害ガスを発生して大気を
汚染するという問題があり、安全に投棄または再利用す
ることが可能な状態に加工する確実且つ無公害な手段が
なかった、という点である。
The problem to be solved by the present invention is that the conventional method, which is accepted as a method for treating waste residues so as not to elute harmful heavy metals, completely elutes even when solidified. However, there is a problem of environmental pollution that cannot be prevented, and if vitrification or sintering is measured, not only is it economically disadvantageous to the facility, but it also causes the problem of generating harmful gas and polluting the atmosphere. Alternatively, there was no reliable and pollution-free means of processing into a reusable state.

【0008】[0008]

【課題を解決するための手段】本発明は前記課題を解決
し、水溶性の金属ハロゲン化物、殊に金属塩化物を含有
する廃棄物残渣を安全に投棄または再利用可能な状態に
処理する確実且つ無公害な手段を提供することを目的と
するものであって、廃棄物残渣を乾燥粉末状としてこれ
に金属酸化物の粉末を添加混合し、この混合物に水蒸気
を通気しながら加熱して金属ハロゲン化物を分解させる
こととした。
The present invention solves the above problems and ensures that waste residues containing water-soluble metal halides, especially metal chlorides, can be safely dumped or treated in a reusable state. The purpose of the present invention is to provide a non-polluting means, in which the waste residue is made into a dry powder form and mixed with a powder of a metal oxide, and the mixture is heated while aerating steam to heat the metal. It was decided to decompose the halide.

【0009】金属ハロゲン化物は熱により分解されてハ
ロゲン水素ガスを発生するが、これは水蒸気に捕捉され
るので混合物を通過した水蒸気を冷却凝縮することによ
りハロゲン水素水として安全に回収されることとなる。
また、分解により生成した金属はその殆んどが水に不溶
の酸化物となり、そのまま処理物に残留させても雨水な
どにより溶出することがなく、従って埋立て地などに投
棄しても安全である。更に、処理物をセメントモルタ
ル、高分子物質などで固化し建築、構築材料に再生して
も同じ理由により環境汚染の心配なく屋外で使用するこ
とができる。更にまた、ガラス化或いは焼結により再利
用可能な状態に高熱処理する際に有害ガスを発生するこ
とがないので、設備の腐食や大気汚染を伴うことなく処
理することができる。
The metal halide is decomposed by heat to generate halogen hydrogen gas, which is trapped by water vapor and therefore can be safely recovered as halogen hydrogen water by cooling and condensing the water vapor that has passed through the mixture. Become.
In addition, most of the metal produced by decomposition becomes an insoluble oxide in water, and even if it remains in the treated product as it is, it will not elute due to rainwater, etc., so it is safe to dispose of in landfills. is there. Furthermore, even if the treated product is solidified with cement mortar, polymer substance or the like and recycled as a building or building material, it can be used outdoors without fear of environmental pollution for the same reason. Furthermore, since no harmful gas is generated during the high heat treatment to a reusable state by vitrification or sintering, the treatment can be performed without causing equipment corrosion or air pollution.

【0010】次に、廃棄物残渣が焼却灰である場合は既
に乾燥粉末状であるのでそのまま処理することができ
る。しかし、廃棄物残渣が例えば下水道最終処理場で生
じた沈殿物のように水分を含んだ汚泥物である場合は天
日により或いは低温加熱により水分を蒸発除去して乾燥
したものを粉末状に砕く、という前処理が必要である。
尚、この前処理は水分の蒸発が可能な程度の低い温度で
行なうことにより、金属ハロゲン化物は分解することな
く残留する。
When the waste residue is incinerated ash, it can be treated as it is because it is already in the form of dry powder. However, if the waste residue is a sludge containing water such as a sediment produced at the final sewer treatment plant, it is dried by sun or by low-temperature heating to evaporate the water and crush it into powder. , Pretreatment is required.
The pretreatment is carried out at a temperature low enough to evaporate water, so that the metal halide remains without being decomposed.

【0011】このように乾燥粉末状とすることにより、
分解促進の触媒として働く金属酸化物の粉末を均一に混
合することができるとともに、水蒸気をまんべんなく接
触させて通すことができる。また、金属酸化物として
は、酸化アルミニウム、酸化第二鉄、酸化タングステン
が好ましい物質として例示され、これらの一種または二
種以上を添加使用する。
By thus forming a dry powder,
The powder of the metal oxide that acts as a catalyst for promoting the decomposition can be uniformly mixed, and the steam can be evenly contacted and passed. As the metal oxide, aluminum oxide, ferric oxide, and tungsten oxide are exemplified as preferable substances, and one or more of these are added and used.

【0012】これらの廃棄物残渣と金属酸化物とは前者
対後者の割合(重量比)が9:1〜2:8の範囲、好ま
しくは9:1〜5:5の範囲で混合するのがよい。即
ち、金属酸化物が重量比10%を下回ると廃棄物残渣に
対する絶対量が不足し充分な効果が得られない。また、
金属酸化物の割合を大きくするのは有効であるが、一定
以上では効果が比例しないため無駄であるので重量比5
0%以下とするのが経済的に好ましい。
The waste residue and the metal oxide are mixed in a ratio (weight ratio) of the former to the latter in the range of 9: 1 to 2: 8, preferably 9: 1 to 5: 5. Good. That is, if the metal oxide content is less than 10% by weight, the absolute amount with respect to the waste residue is insufficient and a sufficient effect cannot be obtained. Also,
It is effective to increase the ratio of metal oxides, but if the ratio is more than a certain level, the effect is not proportional and it is useless.
It is economically preferable to set it to 0% or less.

【0013】更に、混合物に通気させる水蒸気は廃棄物
残渣1Kgに対し凝縮液換算で1〜10L相当とし、且
つ加熱温度は金属ハロゲン化物を触媒の存在下で活発に
分解可能な600℃以上、好ましくは600〜1100
℃の範囲とする。そして、水蒸気を通気させながらこの
加熱温度範囲内に0,5〜6時間、好ましくは1〜3時
間維持することにより、金属ハロゲン化物が高濃度で含
有されていてもはぼ完全に分解し且つ発生したハロゲン
水素ガスをほぼ完全に捕捉し回収することができる。こ
の間、混合物は放置しておいてもよいが適宜撹拌するこ
とにより水蒸気との接触を均等化し効率を高めることが
できる。即ち、加熱温度は高い方が有効であるが、徒ら
に高くしても熱消費量の増大、設備の劣化を招くので1
100℃以下とするのがよい。また、加熱時間は長い方
が有効と思われるが、徒らに長くしても分解がほぼ完了
しているものを加熱しつづけることとなるので3時間以
内にとどめるのが好ましい。
Further, the steam to be aerated in the mixture is equivalent to 1 to 10 L in terms of condensate with respect to 1 kg of waste residue, and the heating temperature is 600 ° C. or higher, which is capable of actively decomposing metal halides in the presence of a catalyst, preferably Is 600 to 1100
It shall be in the range of ° C. By maintaining this heating temperature range for 0.5 to 6 hours, preferably 1 to 3 hours while aerating water vapor, the metal halide is completely decomposed even if it is contained at a high concentration and The generated halogen hydrogen gas can be almost completely captured and recovered. During this time, the mixture may be allowed to stand, but by appropriately stirring it, the contact with the steam can be equalized and the efficiency can be improved. That is, the higher the heating temperature is, the more effective the heating temperature is.
The temperature is preferably 100 ° C or lower. Further, it seems that a longer heating time is effective, but it is preferable to keep the heating time within 3 hours because even if the heating time is long, the one whose decomposition is almost completed is continued to be heated.

【0014】ハロゲン水素ガスを捕捉した水蒸気の凝縮
液は主として塩酸水溶液であって、塩化水素ガスなどの
有害ガスは大気中に放散することなく回収され、且つ揮
発した水銀などもこの水溶液中に回収され、更にカドミ
ウム、鉛、亜鉛などは無害の酸化物として回収すること
ができる。
The condensate of water vapor in which halogen hydrogen gas is captured is mainly an aqueous solution of hydrochloric acid, and harmful gas such as hydrogen chloride gas is recovered without being diffused into the atmosphere and volatilized.
Emitted mercury and the like are also recovered in this aqueous solution, and cadmium, lead, zinc and the like can be recovered as harmless oxides.

【0015】処理済みの廃棄物残渣には金属ハロゲン化
物の分解により生成した金属の酸化物および触媒として
添加した金属酸化物が残存しているが、これらは殆んど
が水に不溶であり、有害重金属含有量が規準値以下であ
ればそのまま投棄可能である。また、固化、ガラス化、
焼結などにより再利用を計った際の使用時、加工時に有
害物質の放出や溶出がなくきわめて安全である
The treated waste residue contains metal oxides produced by decomposition of metal halides and metal oxides added as catalysts, but most of these are insoluble in water. If the harmful heavy metal content is below the standard value, it can be discarded as it is. In addition, solidification, vitrification,
It is extremely safe because it does not release or elute harmful substances during use and processing when it is reused after sintering .

【0016】図1は本発明による処理を行なう設備の一
例を概略的に示したものであって、電気炉のような加熱
炉1の内部に処理室2を設けて廃棄物残渣と金属酸化物
との混合物3を薄く拡げて載せた皿状の容器4を一個ま
たは容積に応じて二個以上収納し、この処理室2の両端
に蒸気発生機5から延びる蒸気導入管6と凝縮機7に至
る回収管8とを接続した構成である。
FIG. 1 schematically shows an example of equipment for carrying out the treatment according to the present invention, in which a treatment chamber 2 is provided inside a heating furnace 1 such as an electric furnace to dispose of waste residues and metal oxides. One or two or more dish-shaped containers 4 in which the mixture 3 of and is placed thinly are placed, and a steam introduction pipe 6 and a condenser 7 extending from a steam generator 5 are provided at both ends of the processing chamber 2. This is a configuration in which all the collecting tubes 8 are connected.

【0017】前述の水蒸気通気量、加熱温度、加熱時間
で混合物3を処理し、凝縮機7で凝縮したハロゲン水素
の水溶液は回収容器9に溜められ、更に利用するかまた
は廃棄するものである。
The mixture 3 is treated with the amount of steam permeation, the heating temperature and the heating time described above, and the aqueous solution of halogen hydrogen condensed in the condenser 7 is stored in the recovery container 9 for further use or disposal.

【0018】[0018]

【実施例】都市清掃工場の焼却炉で生じた焼却灰および
下水道最終処理場で生じた沈殿物である汚泥物を天日乾
燥したものの所定量と分解促進剤である酸化アルミニウ
ムとをそれぞれ充分に粉砕混合して試料を調整し、焼却
灰および汚泥物のみからなる試料と比較した。各試料の
配合割合(重量比)は表1、表2の通りである。
[Examples] A predetermined amount of incineration ash generated in an incinerator of an urban cleaning plant and sludge that is a sediment generated in a sewer final treatment plant are dried in the sun and aluminum oxide that is a decomposition accelerator is sufficiently added. Samples were prepared by crushing and mixing, and compared with samples consisting only of incinerated ash and sludge. The blending ratio (weight ratio) of each sample is as shown in Tables 1 and 2.

【0019】[0019]

【表1】 [Table 1]

【0020】[0020]

【表2】 [Table 2]

【0021】試料の5gを磁性皿に入れ、予め1000
℃に加熱しておいた電気炉に入れ、水蒸気を通気しなが
ら1000℃に6時間保持した。水蒸気の通気量は合計
で凝縮液換算1500ccである。処理後の試料に希硝
酸を加え加温して塩化物を溶解しろ過して得たろ液につ
いて、塩素イオン電極法および硝酸銀溶液を滴定液とす
る自動滴定装置を用いて残留塩素イオン量を測定し、表
3および表4の結果を得た。
5 g of the sample was placed in a magnetic dish, and 1000
It was placed in an electric furnace that had been heated to 0 ° C., and kept at 1000 ° C. for 6 hours while ventilating steam. The total flow rate of water vapor is 1500 cc in terms of condensate. For the filtrate obtained by adding dilute nitric acid to the treated sample and heating it to dissolve the chloride and filtering it, measure the residual chloride ion amount using the chloride ion electrode method and an automatic titrator using a silver nitrate solution as the titrant. The results shown in Tables 3 and 4 were obtained.

【0022】[0022]

【表3】 [Table 3]

【0023】[0023]

【表4】 [Table 4]

【0024】これらから、触媒である金属酸化物を10
重量比以上添加することにより、有害ガスとなるハロゲ
ン、殊に塩素をほぼ完全に分離除去できることが判っ
た。尚、50重量比を越えると効果はほぼ横ばいとなる
ので、経済性を考えて金属酸化物の添加範囲は10〜5
0重量比とするのがよいことも判った。
From these, the catalyst metal oxide 10
It was found that halogen, particularly chlorine, which is a harmful gas, can be separated and removed almost completely by adding more than the weight ratio. If the amount exceeds 50% by weight, the effect is almost leveled off. Therefore, considering the economical efficiency, the addition range of the metal oxide is 10-5.
It has also been found that a 0 weight ratio is preferred.

【0025】次に、酸化アルミニウム20重量比とした
試料を用いて加熱温度を変えた場合の残留塩素イオン量
の測定結果を表5に示す。但し、加熱時間はいずれも6
時間である。これにより、加熱温度が高い方が有効であ
ることが判った。
Next, Table 5 shows the measurement results of the amount of residual chlorine ions when the heating temperature was changed using a sample in which the weight ratio of aluminum oxide was 20. However, the heating time is 6
It's time. From this, it was found that the higher heating temperature is more effective.

【0026】[0026]

【表5】 [Table 5]

【0027】また、酸化アルミニウム20重量比とした
試料を用いて加熱時間を変えた場合の残留塩素イオン量
の測定結果を表6に示す。但し、加熱温度はいずれも1
000℃である。これにより、塩素をほぼ完全に分離除
去するには1時間以上の加熱を必要とするが、従らに長
時間加熱しても効果は殆んど向上せず、経済性を考えて
1〜3時間とするのがよいことが判った。
Table 6 shows the measurement results of the residual chlorine ion amount when the heating time was changed using a sample in which the weight ratio of aluminum oxide was 20. However, the heating temperature is 1
It is 000 ° C. Therefore, in order to almost completely separate and remove chlorine, heating for 1 hour or more is required, but even if it is heated for a long time, the effect is hardly improved. It turned out to be good time.

【0028】[0028]

【表6】 [Table 6]

【0029】更に、酸化アルミニウム20重量比とした
試料を用いて水蒸気の通気量を変えた場合の残留塩素イ
オン量の測定結果を表7に示す。但し、加熱温度は10
00℃、加熱時間は6時間である。これにより、水蒸気
の通気量が多い方が有効であることが判った。
Further, Table 7 shows the measurement results of the amount of residual chlorine ions when the amount of aeration of water vapor was changed using a sample in which the weight ratio of aluminum oxide was 20. However, the heating temperature is 10
The heating time is 00 ° C. and the heating time is 6 hours. From this, it was found that the larger the amount of vapor permeation, the more effective.

【0030】[0030]

【表7】 [Table 7]

【0031】[0031]

【発明の効果】以上の説明から明らかなように、水に溶
解し或いは熱分解して環境汚染の原因となる金属ハロゲ
ン化物を環境汚染の心配がない金属酸化物を触媒として
熱分解し発生したハロゲン水素ガスを水蒸気で捕捉する
ようにした本発明によると、きわめて高い効率で金属ハ
ロゲン化物を金属酸化物とハロゲン水素ガスとに分ける
とともにガスを完全に回収して大気中に放散させること
なく安全に処理することができるものである。そして、
本発明により処理された廃棄物残渣は水溶性および熱分
解性の金属ハロゲン化物が分解除去されていることによ
り、そのまま投棄しても安全であり、また再利用のため
加工し且つ使用しても安全である。
As is apparent from the above description, a metal halide which is dissolved in water or thermally decomposes to cause environmental pollution is thermally decomposed using a metal oxide as a catalyst which does not cause environmental pollution. According to the present invention in which halogen hydrogen gas is captured by water vapor, it is possible to separate metal halide into metal oxide and halogen hydrogen gas with extremely high efficiency, and to safely recover the gas without releasing it into the atmosphere. It can be processed into. And
The waste residue treated according to the present invention is safe to discard as it is because the water-soluble and heat-decomposable metal halides are decomposed and removed, and is also processed and used for reuse. It's safe.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明を実施する設備の一例の配置図。FIG. 1 is a layout diagram of an example of equipment for implementing the present invention.

【符号の説明】[Explanation of symbols]

1 加熱炉, 5 蒸気発生機, 7 凝縮機, 1 heating furnace, 5 steam generator, 7 condenser,

フロントページの続き (58)調査した分野(Int.Cl.7,DB名) B09B 3/00 - 5/00 C02F 11/00 - 11/20 Continuation of front page (58) Fields surveyed (Int.Cl. 7 , DB name) B09B 3/00-5/00 C02F 11/00-11/20

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 廃棄物残渣を乾燥粉末状としてこれに金
属酸化物の粉末を添加混合し、この混合物に水蒸気を通
気しながら加熱して金属ハロゲン化物を分解させること
を特徴とする廃棄物残渣の処理方法。
1. A waste residue, characterized in that the waste residue is made into a dry powder form, and a powder of a metal oxide is added to and mixed with the waste residue, and the mixture is heated while aerating steam to decompose the metal halide. Processing method.
【請求項2】 乾燥粉末状の廃棄物残渣と粉末の金属酸
化物とを重量比で9:1〜5:5の範囲で混合し、60
0〜1100℃の加熱温度で1〜3時間維持する請求項
1記載の処理方法。
2. A dry powdery waste residue and a powdered metal oxide are mixed in a weight ratio of 9: 1 to 5: 5, and 60
The processing method according to claim 1, wherein the heating temperature is maintained at 0 to 1100 ° C for 1 to 3 hours.
【請求項3】 金属酸化物が酸化アルミニウム、酸化第
二鉄、酸化タングステンの一種または二種以上である請
求項1,2いずれか記載の処理方法。
3. The processing method according to claim 1, wherein the metal oxide is one kind or two or more kinds of aluminum oxide, ferric oxide, and tungsten oxide.
JP07962394A 1994-03-25 1994-03-25 Waste residue treatment method Expired - Fee Related JP3440246B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP07962394A JP3440246B2 (en) 1994-03-25 1994-03-25 Waste residue treatment method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP07962394A JP3440246B2 (en) 1994-03-25 1994-03-25 Waste residue treatment method

Publications (2)

Publication Number Publication Date
JPH07256230A JPH07256230A (en) 1995-10-09
JP3440246B2 true JP3440246B2 (en) 2003-08-25

Family

ID=13695204

Family Applications (1)

Application Number Title Priority Date Filing Date
JP07962394A Expired - Fee Related JP3440246B2 (en) 1994-03-25 1994-03-25 Waste residue treatment method

Country Status (1)

Country Link
JP (1) JP3440246B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW510830B (en) * 1999-08-10 2002-11-21 Sumitomo Metal Ind Method for treating hazardous material

Also Published As

Publication number Publication date
JPH07256230A (en) 1995-10-09

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