JP2695589B2 - Exhaust gas and dust collection method - Google Patents

Exhaust gas and dust collection method

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Publication number
JP2695589B2
JP2695589B2 JP5012928A JP1292893A JP2695589B2 JP 2695589 B2 JP2695589 B2 JP 2695589B2 JP 5012928 A JP5012928 A JP 5012928A JP 1292893 A JP1292893 A JP 1292893A JP 2695589 B2 JP2695589 B2 JP 2695589B2
Authority
JP
Japan
Prior art keywords
exhaust gas
dust
ash
alkali
acid
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 - Fee Related
Application number
JP5012928A
Other languages
Japanese (ja)
Other versions
JPH06218224A (en
Inventor
正坦 岸田
誠 北野
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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Filing date
Publication date
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Priority to JP5012928A priority Critical patent/JP2695589B2/en
Publication of JPH06218224A publication Critical patent/JPH06218224A/en
Application granted granted Critical
Publication of JP2695589B2 publication Critical patent/JP2695589B2/en
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Expired - Fee Related legal-status Critical Current

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Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/20Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters

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、都市ごみ、産業廃棄物
などの固形廃棄物の焼却炉,石炭焚ボイラー,廃液焼却
炉,電気炉,非鉄溶解炉などの酸性ガス(例えば、HC
l,SOx,NOx,HF)を含み、かつ、排ガスに同
伴されるダスト中に重金属(例えば、Pb,Zn,C
d,Hg)を含む各種の炉から排出される排ガスと集塵
灰の無害化処理方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an acidic gas (such as HC, for example, an incinerator for solid waste such as municipal solid waste and industrial waste, a coal-fired boiler, a waste liquid incinerator, an electric furnace, a non-ferrous melting furnace, etc.
1, SOx, NOx, HF), and heavy metals (for example, Pb, Zn, C) in the dust entrained in the exhaust gas.
d, Hg), and exhaust gas discharged from various furnaces and dust ash.

【0002】[0002]

【従来の技術】都市ごみや産業廃棄物排出量の増加と焼
却率の増加に伴い、焼却排ガス及び集塵灰,焼却灰や各
種工場設備における排ガス及び集塵灰の発生量が増え、
その中に含まれる酸性ガスや重金属が新しい環境汚染源
となっている。
2. Description of the Related Art With the increase in the amount of municipal waste and industrial waste discharged and the increase in the incineration rate, the amount of incineration exhaust gas and dust ash, incinerator ash, and the amount of exhaust gas and dust ash generated in various factory facilities increase,
Acid gases and heavy metals contained in them are new sources of environmental pollution.

【0003】このうち、とくに、有機ごみ焼却炉の排ガ
スは、HCl,SOx,NOx,HFなどの有害な酸性
ガスを多く含有し、かつ、灰は水銀、亜鉛、鉛などの低
沸点重金属を多く含有し、これらが環境に放出された場
合雨水などに溶解して酸性雨となり、また、灰からは有
害な重金属が溶出するため、その防止技術が種々開発さ
れてきた。
Of these, in particular, the exhaust gas of the organic refuse incinerator contains a lot of harmful acidic gases such as HCl, SOx, NOx and HF, and the ash contains a lot of low boiling heavy metals such as mercury, zinc and lead. When they are contained and released into the environment, they dissolve in rainwater or the like to become acid rain, and harmful heavy metals are eluted from ash, and various prevention techniques have been developed.

【0004】たとえば、酸性ガス捕集のために、アルカ
リ洗浄塔方式,半湿式石灰乳の移動充填層反応方式,乾
式の消石灰吹込み方式が各地で採用されている。
For example, in order to collect the acidic gas, an alkali washing tower system, a semi-wet lime milk moving packed bed reaction system, and a dry slaked lime blowing system are adopted in various places.

【0005】また、灰の無害化方法としては、「環境施
設」No.21(1985)p.79〜84には、コン
クリートと混練して固化する方法や、灰より水抽出した
重金属を炭酸ガスと反応させて炭酸塩化する方法、アス
ファルトと混合させて固化させる方法等が記載されてい
る。
As a method for detoxifying ash, "Environmental Facility" No. 21 (1985) p. 79 to 84, a method of kneading and solidifying with concrete, a method of reacting a heavy metal extracted from ash with water with carbon dioxide to carbonate, a method of mixing with asphalt to solidify are described.

【0006】また、特公昭61−47154号公報に
は、重金属を含有する廃棄物灰に、鉄塩の存在の下でア
ルカリ成分を加えて混合し、この混合物を造粒あるいは
静置状態で300℃以下に保持することによって、重金
属を鉄塩との混合水酸化物として固定することが開示さ
れている。
In Japanese Patent Publication No. 61-47154, a waste ash containing a heavy metal is mixed with an alkaline component in the presence of an iron salt and mixed, and the mixture is granulated or allowed to stand at a temperature of 300. It is disclosed that the heavy metal is fixed as a mixed hydroxide with an iron salt by maintaining the temperature at or below ° C.

【0007】これによって、灰中の重金属は相当割合固
定されて、安全な投棄が可能になるという利点があると
している。
It is said that the heavy metal in the ash is fixed to a considerable extent, and there is an advantage that it can be safely dumped.

【0008】しかしながら、この重金属の固定法は、ア
ルカリを処理灰に直接添加して混合するものであるの
で、該処理のために、高価なアルカリが必要であり、ま
た、混合が不充分であると部分的にpHが高くなり、p
Hが11.5以上になると、重金属が固定できなくな
り、固定化の効率が低下し、しかも、常温付近では2日
間の処理時間を要し、処理時間の長期化又は処理設備が
膨大になるという欠点がある。
However, in this heavy metal fixing method, an alkali is directly added to the treated ash and mixed, so that an expensive alkali is required for the treatment, and the mixing is insufficient. Partly the pH becomes high and p
When H is 11.5 or more, heavy metals cannot be fixed, the efficiency of immobilization decreases, and moreover, the treatment time of 2 days is required at around room temperature, and the treatment time becomes long or the treatment facility becomes huge. There are drawbacks.

【0009】また、アルカリを処理灰に添加しているた
め、排ガス中に含まれる有害な酸性ガスの捕集は、一切
行なえない欠点を有する。
Further, since alkali is added to the treated ash, there is a drawback that the harmful acid gas contained in the exhaust gas cannot be collected at all.

【0010】[0010]

【発明が解決しようとする課題】本発明の目的は、酸性
ガス成分及び重金属成分を含む各種可燃物を焼却又は溶
融,乾留などを行なう設備から発生する酸性ガスを含む
排ガス及び排ガスから捕集された重金属を含む集塵灰及
び焼却残渣を無害化する経済的な方法を提供することに
ある。
SUMMARY OF THE INVENTION An object of the present invention is to collect various combustible substances containing an acidic gas component and a heavy metal component from exhaust gas and exhaust gas containing an acidic gas generated from equipment for incineration or melting and carbonization. Another object of the present invention is to provide an economical method for detoxifying dust ash and incineration residue containing heavy metals.

【0011】[0011]

【課題を解決するための手段】本発明は、処理炉からの
排ガス中にアルカリ又はアルカリと粉末状の2価鉄塩
噴霧し、排ガス中の酸性ガスを無害化処理する第1工程
に続き、該アルカリ又はアルカリと粉末状の2価鉄塩
添加した排ガス中のダストを集塵する第2工程を有する
とともに、前記集塵ダストに対して、水,2価鉄塩及び
を加えた後、攪拌・加熱する第3工程とを有すること
を特徴とする排ガス及び集塵ダストの処理方法である。
The present invention follows the first step of detoxifying acid gas in exhaust gas by spraying alkali or alkali and powdery divalent iron salt into exhaust gas from a processing furnace. And a second step of collecting dust in the exhaust gas to which the alkali or alkali and powdery divalent iron salt has been added, and water, divalent iron salt and
And a third step of stirring and heating after adding an acid .

【0012】[0012]

【作用】ダスト,SOx,HClなどを含有する排ガス
に、集塵装置の上流側でアルカリを添加することによ
り、排ガス中のSOxやHClなどの酸性有害物質がア
ルカリと反応し、排ガス中から除去される。
[Function] By adding an alkali to the exhaust gas containing dust, SOx, HCl, etc. at the upstream side of the dust collector, acidic harmful substances such as SOx and HCl in the exhaust gas react with the alkali and are removed from the exhaust gas. To be done.

【0013】更に、アルカリを排ガスである気流中に添
加するため、重金属を含む粉塵とアルカリとの混合が促
進され、後のフェライト化処理にとって好ましくなる。
Further, since the alkali is added to the air flow which is the exhaust gas, the mixing of the dust containing the heavy metal and the alkali is promoted, which is preferable for the subsequent ferrite treatment.

【0014】また、排ガス中のSOxやHCl濃度によ
っては、アルカリ添加量が多量に必要となり、その結果
重金属を含む集塵ダストとアルカリとの混合物のpHが
高くなるとフェライト化反応には不適となる。このよう
な場合に酸を添加してフェライト化反応を促進させる。
Further, depending on the concentration of SOx or HCl in the exhaust gas, a large amount of alkali must be added. As a result, if the pH of the mixture of dust and dust containing heavy metals and alkali becomes high, it becomes unsuitable for the ferrite formation reaction. . In such a case, an acid is added to accelerate the ferritization reaction.

【0015】なお、次操作の2価鉄源として、粉末状の
2価鉄塩を使う場合は、アルカリと同様排ガス中に添加
して、混合効果を上げる方法も有効である。
When a powdery divalent iron salt is used as the divalent iron source for the next operation, it is effective to add it to the exhaust gas in the same manner as the alkali to enhance the mixing effect.

【0016】次に、集塵灰のフェライト化処理について
説明する。
Next, the ferritizing treatment of the collected ash will be described.

【0017】集塵灰に混練用の水を添加して、この湿状
態の混合物に、2価鉄と酸を加えて両者を均一に混合物
中に分散させる。この混合物のpHを7.0〜11.5
に調整した後温度を30〜99℃に維持することによ
り、混合物中の2価鉄は次第に結晶化してフェライトに
変わって行く。フェライトとは化学式でMFe2
4(M:Fe,Zn,Pbなどの金属)で表されるもの
で、混合物中の2価鉄がフェライトといわれる鉄酸化物
の結晶格子を形成して行く過程で、重金属が本来鉄の原
子が占めるべき位置に鉄の代わりに取り込まれて固定化
する。
Water for kneading is added to the collected ash, and divalent iron and acid are added to this wet mixture to uniformly disperse both of them. The pH of this mixture is 7.0-11.5.
By adjusting the temperature to 30 ° C. to 99 ° C. after the adjustment, the divalent iron in the mixture gradually crystallizes and turns into ferrite. Ferrite is a chemical formula of MFe 2 O
4 (M: Fe, Zn, Pb, and other metals), the divalent iron in the mixture forms the iron oxide crystal lattice called ferrite, and the heavy metal is originally an iron atom. Instead of iron, it is taken in and fixed at the position that should be occupied by.

【0018】その反応式は次のように表される。The reaction formula is expressed as follows.

【0019】中和反応:M2++2Fe2++6OH- →M
Fe2+(OH)6 (1) 酸化反応:MFe2 (OH)6 +1/2O2 →MFe2
4 +3H2 O (2) 上記反応式において、pHが
7.0より少ないと、(1)式の反応におけるOH- が
不足してフェライト化反応が進まない。また、pHが1
1.5を超えると重金属、例えば鉛はHPbO2 - の形
態をとり、フェライト化反応に取り込まれない。また、
酸素がない場合や酸素との接触のないとき、例えば静置
など、混合物を攪拌しない場合には(2)式におけるO
2 が不足して、反応が進まない。
Neutralization reaction: M 2+ + 2Fe 2+ + 6OH → M
Fe 2+ (OH) 6 (1) Oxidation reaction: MFe 2 (OH) 6 + 1 / 2O 2 → MFe 2
O 4 + 3H 2 O (2) In the above reaction formula, if the pH is less than 7.0, OH − in the reaction of the formula (1) will be insufficient and the ferrite formation reaction will not proceed. Also, the pH is 1
If it exceeds 1.5, heavy metals such as lead take the form of HPbO 2 − and are not incorporated in the ferritization reaction. Also,
When there is no oxygen or when there is no contact with oxygen, and when the mixture is not stirred, for example, when it is allowed to stand, the O
2 is insufficient and the reaction does not proceed.

【0020】更に、フェライト化反応における前記酸化
反応(2)を促進させるため、少なくとも加熱すること
が有効であり、30℃以上の加熱が必要である。
Furthermore, in order to promote the oxidation reaction (2) in the ferrite formation reaction, at least heating is effective and heating at 30 ° C. or higher is required.

【0021】また、加熱温度が100℃以上では、酸化
反応(2)における酸素の水への溶解度が殆ど零に近く
なり酸化反応が進まないため、加熱温度は100℃未満
にする必要がある集塵灰中へ添加する2価鉄塩及び酸
しては、水溶液の形で混合することが処理上好適であ
り、2価鉄塩は硫酸塩、塩化物として、また、酸として
は硫酸、塩酸、更に集塵装置の排ガス上流測で添加する
アルカリとしては、消石灰などを用いることができる。
When the heating temperature is 100 ° C. or higher, the solubility of oxygen in water in the oxidation reaction (2) is almost zero and the oxidation reaction does not proceed. Therefore, the heating temperature needs to be lower than 100 ° C. is to <br/> 2 Ataitetsushio及beauty acid added into Chirihai, be mixed in the form of an aqueous solution are preferred over process, 2 Ataitetsushio is sulfate, as chlorides, also, Sulfuric acid, hydrochloric acid can be used as the acid, and slaked lime or the like can be used as the alkali added in the upstream measurement of the exhaust gas from the dust collector.

【0022】集塵灰に対する2価鉄塩及び酸の配合量
は、その反応に要する化学当量よりも多く要するが、通
常10〜200%増程度で十分機能は果たせる。しか
し、この添加量は重金属の形態などによって変わってく
るため、予備試験後決定するのが好ましい。
[0022] The amount of 2 Ataitetsushio及beauty acid to dust collection ash, it takes more than the chemical equivalent required for the reaction, typically function well at about up 10 to 200% may play. However, since the amount of addition depends on the form of the heavy metal and the like, it is preferable to determine after the preliminary test.

【0023】[0023]

【実施例】実施例1 図1は、使用した処理設備の概要を示す。EXAMPLES Example 1 FIG. 1 shows an outline of the processing equipment used.

【0024】同図において、12は電気集塵機13の上
流側の排ガスダクトに設けられた粉体噴出装置を示し、
焼却炉からの排ガスE中に粉体噴出装置12を介してア
ルカリとして消石灰Cを供給し、排ガス中の塩化水素及
び硫黄酸化物との反応を行なわせた。
In the figure, reference numeral 12 denotes a powder ejection device provided in an exhaust gas duct on the upstream side of the electrostatic precipitator 13,
Slaked lime C was supplied as an alkali into the exhaust gas E from the incinerator through the powder ejection device 12 to cause a reaction with hydrogen chloride and sulfur oxides in the exhaust gas.

【0025】ここで消石灰Cは粉体でHClに対し、反
応モル当量比で2.0倍の割合で噴出した。この操作に
より排ガス中のHClを95%除去した。
Here, slaked lime C was sprayed as a powder at a ratio of 2.0 times the reaction molar equivalent ratio to HCl. By this operation, 95% of HCl in the exhaust gas was removed.

【0026】供給した消石灰、反応した塩化カルシウ
ム、硫酸カルシウムは焼却炉飛灰と共に電気集塵機13
により捕集した。この捕集灰A(以下EP灰)は灰出し
用のロータリーバルブ14を介して、EP灰貯留槽15
に貯留され、EP灰貯留槽15下部の定量切出しフィー
ダ16から排出され、リアクター1に受入れた。このE
P灰Aは排ガス中へのアルカリの添加によってpHが1
2.0であるため、重量比3%の硫酸Fをタンク3から
水溶液状態で受け入れ、混合物のpHを11.5とする
ように調整した。これをリアクター1内で空気を混合物
乾物重量1kg当たり10リットル/minの割合で、
空気導入口4から通気しながら、混合物の温度が70℃
になるように加熱装置6によって加熱し、かつ連続的に
撹拌機7を用いて撹拌し、表1と表2に示す結果を得
た。
The supplied slaked lime, reacted calcium chloride, and calcium sulfate were collected by the electric dust collector 13 together with the incinerator fly ash.
Collected by. The collected ash A (hereinafter referred to as EP ash) is passed through a rotary ash discharging valve 14 and is passed through an EP ash storage tank 15
Was stored in the reactor 1 and discharged from the quantitative cut-out feeder 16 below the EP ash storage tank 15 and received in the reactor 1. This E
P ash A has a pH of 1 due to the addition of alkali into the exhaust gas.
Since it was 2.0, the sulfuric acid F in a weight ratio of 3% was received as an aqueous solution from the tank 3, and the pH of the mixture was adjusted to 11.5. This is mixed with air in the reactor 1 at a rate of 10 liter / min per 1 kg of dry matter of the mixture,
While ventilating from the air inlet 4, the temperature of the mixture is 70 ° C.
It was heated by the heating device 6 so as to be, and continuously stirred using the stirrer 7, and the results shown in Table 1 and Table 2 were obtained.

【0027】表1は捕集灰Aの重金属の含有量を示し、
表2は処理後の灰の溶出試験結果をコンクリート固化
法、アスファルト固化法と比較して、海洋投棄基準とと
もに示す。溶出試験方法は、環境庁告示第13号(19
73年)による方法を用いた。
Table 1 shows the content of heavy metals in the collected ash A,
Table 2 shows the results of the leaching test of the ash after the treatment in comparison with the concrete solidification method and the asphalt solidification method, together with the ocean dumping standard. For the dissolution test method, refer to the Environmental Agency Notification No. 13 (19
1973) was used.

【0028】[0028]

【表1】 表2に示すように、本実施例の場合、何れの重金属も海
洋投棄基準以下であり、コンクリート固化法、アスファ
ルト固化法と比較して、Pb、Zn、6価Crにおいて
特に優れた結果を示している。
[Table 1] As shown in Table 2, in the case of this example, all the heavy metals were below the ocean dumping standard, and showed particularly excellent results in Pb, Zn, and hexavalent Cr as compared with the concrete solidification method and the asphalt solidification method. ing.

【0029】[0029]

【表2】 その後、換気、撹拌、加熱を行いながら1時間後にリア
クター1の排出口9から取り出し、換気、撹拌、加熱を
行いながら1時間後にリアクター1の排出口9から取り
出し、直径5mm程度に灰処理装置10を用いて造粒し
た。
[Table 2] Then, after ventilating, stirring and heating, it was taken out from the outlet 9 of the reactor 1 hour later, and after ventilation, stirring and heating was taken out from the outlet 9 of the reactor 1 hour later, the ash treatment device 10 having a diameter of about 5 mm was used. Was used for granulation.

【0030】実施例2 図2は、上記実施例1において、リアクター1における
pHの調整のために酸Fとして硫酸水溶液を添加する例
を示す。
Example 2 FIG. 2 shows an example in which an aqueous sulfuric acid solution is added as the acid F in Example 1 to adjust the pH in the reactor 1.

【0031】実施例1と同様に、焼却炉排ガスE中に粉
体噴出装置12を介して消石灰Cを供給し、排ガス中の
塩化水素及び硫黄酸化物との反応を行なわせた。ここで
消石灰Cは粉体でHClに対し、反応モル当量比で2.
0倍の割合で噴出した。この操作により排ガス中のHC
lを95%除去した。
In the same manner as in Example 1, slaked lime C was supplied into the exhaust gas E of the incinerator via the powder jetting device 12 to cause a reaction with hydrogen chloride and sulfur oxides in the exhaust gas. Here, slaked lime C is a powder and has a reaction molar equivalent ratio of 2. to HCl.
Ejected at a rate of 0 times. By this operation, HC in exhaust gas
95% was removed.

【0032】供給した消石灰、反応した塩化カルシウ
ム、硫酸カルシウムは焼却炉飛灰と共に電気集塵機13
により捕集した。この捕集灰A(以下EP灰)は灰出し
用のロータリーバルブ14を介して、EP灰貯留槽15
に貯留され、EP灰貯留槽15下部の定量切出しフィー
ダ16から排出され、リアクター1に受入れた。このE
P灰Aは排ガス中へのアルカリの添加によってpHが1
2.0であるため、重量比3%の硫酸Fをタンク3から
水溶液状態で受け入れ、混合物のpHを11.5とする
ように調整した。これをリアクター1内で空気を混合物
乾物重量1kg当たり10リットル/minの割合で、
空気導入口4から通気しながら、混合物の温度が70℃
になるように加熱装置6によって加熱し、かつ連続的に
撹拌機7を用いて撹拌し、実施例1と同様の結果を得
た。その後、実施例3と同様に造粒処理した。
The supplied slaked lime, reacted calcium chloride, and calcium sulfate were collected together with the incinerator fly ash by the electrostatic precipitator 13.
Collected by. The collected ash A (hereinafter referred to as EP ash) is passed through a rotary ash discharging valve 14 and is passed through an EP ash storage tank 15
Was stored in the reactor 1 and discharged from the quantitative cut-out feeder 16 below the EP ash storage tank 15 and received in the reactor 1. This E
P ash A has a pH of 1 due to the addition of alkali into the exhaust gas.
Since it was 2.0, the sulfuric acid F in a weight ratio of 3% was received as an aqueous solution from the tank 3, and the pH of the mixture was adjusted to 11.5. This is mixed with air in the reactor 1 at a rate of 10 liter / min per 1 kg of dry matter of the mixture,
While ventilating from the air inlet 4, the temperature of the mixture is 70 ° C.
It was heated by the heating device 6 so as to become, and continuously stirred using the stirrer 7, and the same result as in Example 1 was obtained. Then, the granulation process was performed in the same manner as in Example 3.

【0033】[0033]

【発明の効果】本発明によって以下の効果を奏すること
ができる。
According to the present invention, the following effects can be obtained.

【0034】(1)添加すべきアルカリを集塵装置のガ
ス上流側で添加することによって、排ガス中からHCl
等の有害物質を除去すると共に、アルカリを気流中にて
添加するため、集塵ダストとアルカリとの混合が完全に
なり、重金属の溶出防止処理をより完全に行うことがで
きる。また、アルカリは、排ガス中からの有害物質の除
去と集塵灰からの重金属の溶出防止とに有効活用でき
る。
(1) By adding the alkali to be added on the gas upstream side of the dust collector, the HCl is removed from the exhaust gas.
Since the harmful substances such as the above are removed and the alkali is added in the air flow, the dust collection dust and the alkali are completely mixed, and the elution preventing treatment of the heavy metal can be performed more completely. Further, the alkali can be effectively used for removing harmful substances from the exhaust gas and preventing elution of heavy metals from the dust ash.

【0035】(2)短時間で重金属の完全なる固定化が
可能であり、処理時間の大幅な短縮化及び処理設備の大
幅なコンパクト化ができる。
(2) The heavy metal can be completely fixed in a short time, the processing time can be greatly shortened, and the processing equipment can be greatly downsized.

【0036】(3)同時に多種の重金属が処理除去でき
る。
(3) Various heavy metals can be treated and removed at the same time.

【0037】(4)重金属含有量の多少にかかわらず、
低濃度まで処理できる。
(4) Regardless of the heavy metal content,
Can process to low concentrations.

【0038】(5)処理後の灰は磁性を持っているの
で、磁選器で分離でき、その用途拡大が可能となる。
(5) Since the ash after the treatment has magnetism, it can be separated by a magnetic separator and its application can be expanded.

【0039】(6)処理後の灰は自然界に投棄しても再
溶出せず、酸性雰囲気においても安定している。
(6) The ash after the treatment does not re-elute even if it is dumped in the natural world and is stable even in an acidic atmosphere.

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

【図1】 本発明の実施例において用いた処理設備の概
要を示す。
FIG. 1 shows an outline of processing equipment used in an embodiment of the present invention.

【符号の説明】[Explanation of symbols]

1 リアクター 2,3 タンク 4 空気導入口 5 排気ファン 6 加熱装置 7 攪拌機 8 モータ 9 処理済灰の排
出口 10 灰処理装置 11 灰ピット 12 粉体噴出装置 13 電気集塵機 14 ロータリーバルブ 15 灰貯留槽 16 定量切出しフィーダ A 捕集灰 B 硫酸鉄 C 消石灰 D 空気 E 焼却炉排ガス F 硫酸
1 Reactor 2, 3 Tank 4 Air inlet 5 Exhaust fan 6 Heating device 7 Stirrer 8 Motor 9 Discharge port of treated ash 10 Ash treatment device 11 Ash pit 12 Powder ejection device 13 Electrostatic precipitator 14 Rotary valve 15 Ash storage tank 16 Fixed-quantity feeder A Collection ash B Iron sulfate C Slaked lime D Air E Incinerator exhaust gas F Sulfuric acid

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 B09B 3/00 B01D 53/34 136Z ZAB B09B 3/00 ZAB 304G (56)参考文献 特開 昭56−152777(JP,A) 特開 昭58−137490(JP,A) 特開 昭58−137497(JP,A) 特開 平6−134436(JP,A)Continuation of the front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location B09B 3/00 B01D 53/34 136Z ZAB B09B 3/00 ZAB 304G (56) Reference JP-A-56-152777 ( JP, A) JP 58-137490 (JP, A) JP 58-137497 (JP, A) JP 6-134436 (JP, A)

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 処理炉からの排ガス中にアルカリを噴霧
し、排ガス中の酸性ガスを無害化処理する第1工程に続
き、該アルカリを添加した排ガス中のダストを集塵する
第2工程を有するとともに、前記集塵ダストに対して、
水,2価鉄塩及び酸を加えた後、攪拌・加熱する第3工
程とを有することを特徴とする排ガス及び集塵ダストの
処理方法。
1. A first step of spraying alkali into exhaust gas from a processing furnace to detoxify acidic gas in the exhaust gas, and a second step of collecting dust in the exhaust gas to which the alkali is added While having, for the dust collection dust,
And a third step of stirring and heating after adding water, divalent iron salt and acid , and a method for treating exhaust gas and dust collecting dust.
【請求項2】 処理炉からの排ガス中にアルカリ及び粉
末状の2価鉄塩を噴霧し、排ガス中の酸性ガスを無害化
処理する第1工程に続き、該アルカリ及び粉末状の2価
鉄塩を添加した排ガス中のダストを集塵する第2工程を
有するとともに、前記集塵ダストに対して、水及び酸を
加えた後、攪拌・加熱する第3工程とを有することを特
徴とする排ガス及び集塵ダストの処理方法。
2. Alkali and powder in the exhaust gas from the processing furnace
Following the first step of spraying powdery divalent iron salt and detoxifying the acidic gas in the exhaust gas, the alkali and powdery divalent iron
Characterized with a second step of dust collecting dust in the exhaust gas with the addition of iron salts, to the dust collected, after adding Mizu及 beauty acid, that a third step of stirring and heating Exhaust gas and dust collection method.
JP5012928A 1993-01-28 1993-01-28 Exhaust gas and dust collection method Expired - Fee Related JP2695589B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5012928A JP2695589B2 (en) 1993-01-28 1993-01-28 Exhaust gas and dust collection method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5012928A JP2695589B2 (en) 1993-01-28 1993-01-28 Exhaust gas and dust collection method

Publications (2)

Publication Number Publication Date
JPH06218224A JPH06218224A (en) 1994-08-09
JP2695589B2 true JP2695589B2 (en) 1997-12-24

Family

ID=11818984

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5012928A Expired - Fee Related JP2695589B2 (en) 1993-01-28 1993-01-28 Exhaust gas and dust collection method

Country Status (1)

Country Link
JP (1) JP2695589B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996005002A1 (en) * 1994-08-15 1996-02-22 Shinmaywa Industries, Ltd. Heavy metal-containing waste treating process and apparatus
EP0801971A1 (en) * 1995-10-06 1997-10-22 Kaneka Corporation Waste gas and dust treatment method
JP5147146B2 (en) * 2000-05-25 2013-02-20 奥多摩工業株式会社 Waste incineration fly ash treatment method
JP5003887B2 (en) * 2007-07-27 2012-08-15 株式会社Ihi Exhaust gas treatment method and exhaust gas treatment apparatus

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56152777A (en) * 1980-04-25 1981-11-26 Ebara Infilco Co Ltd Treatment of collected dust by waste-matter incinerating facility
JPS58137497A (en) * 1982-02-08 1983-08-15 Ebara Infilco Co Ltd Treatment of heavy metal-containing waste matter
JPS58137490A (en) * 1982-09-01 1983-08-15 Ebara Infilco Co Ltd Treatment of waste matter containing heavy metal

Also Published As

Publication number Publication date
JPH06218224A (en) 1994-08-09

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