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JPS6052876B2 - How to dispose of electrostatically collected ash - Google Patents
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JPS6052876B2 - How to dispose of electrostatically collected ash - Google Patents

How to dispose of electrostatically collected ash

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Publication number
JPS6052876B2
JPS6052876B2 JP55073904A JP7390480A JPS6052876B2 JP S6052876 B2 JPS6052876 B2 JP S6052876B2 JP 55073904 A JP55073904 A JP 55073904A JP 7390480 A JP7390480 A JP 7390480A JP S6052876 B2 JPS6052876 B2 JP S6052876B2
Authority
JP
Japan
Prior art keywords
heavy metal
weight
electrostatically
ash
residue
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
Application number
JP55073904A
Other languages
Japanese (ja)
Other versions
JPS56168873A (en
Inventor
明夫 鈴木
岱輔 西田
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.)
JFE Engineering Corp
Original Assignee
Nippon Kokan Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nippon Kokan Ltd filed Critical Nippon Kokan Ltd
Priority to JP55073904A priority Critical patent/JPS6052876B2/en
Publication of JPS56168873A publication Critical patent/JPS56168873A/en
Publication of JPS6052876B2 publication Critical patent/JPS6052876B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は、ごみ焼却炉等から排出される電気集塵灰の処
理方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for treating electrostatically collected ash discharged from a garbage incinerator or the like.

ごみ焼却炉から排出される電気集塵灰は、ごみ一の種類
によつてて若干異なるが、一般的には第1表に示すよう
にスラグ成分50〜70%、塩化物および硫酸塩25〜
45%を主体とし、その他有害重金属と一般重金属を3
〜5%含んでいる。
Electrostatic precipitated ash discharged from a garbage incinerator differs slightly depending on the type of garbage, but generally, as shown in Table 1, the slag component is 50-70%, and the chloride and sulfate content is 25-25%.
Mainly contains 45% and 3% other harmful heavy metals and general heavy metals.
Contains ~5%.

このうち有害重金属の一部は、水に可溶な塩化物の形態
で存在しこのまま投棄すると有害重金属が第2表の溶出
試験結果に示すように排出規制値を越えて溶出するおそ
れがある。
Some of these toxic heavy metals exist in the form of chlorides that are soluble in water, and if they are dumped as is, there is a risk that the toxic heavy metals will elute beyond the emission regulation value, as shown in the elution test results in Table 2.

このため重金属の溶出を防止する方法として例えばフェ
ライト化による処理方法が提案されている。
For this reason, a treatment method using ferrite formation, for example, has been proposed as a method for preventing the elution of heavy metals.

この方法は、第1図が示すように抽出槽1に重金属を含
む電気集塵灰2、溶解水3及び硫酸4を投入して、これ
をフィルター4で残渣4と重金属イオンを含む溶液5と
に分離する。この残渣4は溶出性重金属塩を低減したた
め投棄可能である。一方溶液6はいわゆるフェライト法
で処理される。この方法は溶液6を硫酸第1鉄7ととも
に溶解槽8に投入し、さらに反応器9内に入れ、アルカ
リ10、蒸気加熱12などによつて所定のPHl温度と
して曝気11により空気酸化する。この過程でFe(0
H)2は重金属を取り込みながらフェライト化する。生
成したフェライトは磁気又は沈降で分離され、フィルタ
ー14により脱水されて、フェライト化スラッジ15と
なるものである。また溶液16はPH調整槽17で中和
された後次工程に入る。しかしこの方法は、硫酸第1鉄
を多量に投入しなければならず、そのランニングコスト
がたかいとともに、多量の溶液がでるため下水などが完
備されていることが条件となる。
In this method, as shown in Fig. 1, electrostatically precipitated ash 2 containing heavy metals, dissolved water 3, and sulfuric acid 4 are put into an extraction tank 1, and then passed through a filter 4 into a residue 4 and a solution 5 containing heavy metal ions. Separate into This residue 4 can be discarded because the amount of leachable heavy metal salts has been reduced. On the other hand, solution 6 is processed by the so-called ferrite method. In this method, a solution 6 is put into a dissolution tank 8 together with ferrous sulfate 7, and then put into a reactor 9, and the solution is brought to a predetermined PHL temperature by alkali 10, steam heating 12, etc., and air oxidized by aeration 11. In this process, Fe(0
H) 2 converts into ferrite while incorporating heavy metals. The generated ferrite is separated by magnetism or sedimentation, dehydrated by a filter 14, and becomes ferrite sludge 15. Further, the solution 16 is neutralized in a pH adjustment tank 17 before entering the next step. However, this method requires a large amount of ferrous sulfate to be added, which is expensive to run, and requires a complete sewage system because a large amount of solution is produced.

更にフェライト化スラッジは、重要な鉄資源よりなるた
め、有効利用が図られなければならない。また別の方法
として、電気集塵灰をアルカリ処理して重金属を水酸化
物に変えたのち助剤を加えペレット化、更にロータリー
キルン等を用いて焼結固化する方法もあるが、ペレット
化焼成など操業上の頻雑さがあるなどの欠点がある。
Furthermore, since ferritic sludge consists of an important iron resource, it must be used effectively. Another method is to treat electrostatic precipitated ash with alkali to convert heavy metals into hydroxides, then add an auxiliary agent to make pellets, and then sinter and solidify using a rotary kiln, etc. There are disadvantages such as operational complexity.

本発明は上記事情に鑑みてなされたもので、その目的と
するところは、有害重金属の溶出を確実に防止でき、し
かも排水の量が少なく、又ランニングコストを小さくす
ることができる電気集塵灰の処理方法を得んとするもの
である。
The present invention has been made in view of the above circumstances, and its purpose is to provide electrostatic precipitated ash that can reliably prevent the elution of harmful heavy metals, reduce the amount of wastewater, and reduce running costs. The purpose of this study is to find a method for processing this.

すなわち本発明は電気集塵灰を酸洗処理して残渣と重金
属イオンを含む溶液とに分離した後該溶液をアルカリ処
理して重金属の水酸化物を沈殿分離せしめ、次いで該重
金属の水酸化物に上記残渣の一部と融剤とを加えて90
0〜1100℃で加熱溶融固化することを特徴とする電
気集塵灰の処理方法である。
That is, in the present invention, electrostatically precipitated ash is pickled to separate it into a residue and a solution containing heavy metal ions, and then the solution is treated with an alkali to precipitate and separate heavy metal hydroxides. Add a part of the above residue and a flux to 90%
This is a method for treating electrostatically precipitated ash, which is characterized by heating and melting and solidifying at 0 to 1100°C.

更に本発明は電気集塵灰を酸洗処理して残渣と重金属イ
オンを含む溶液とに分離した後該溶液をアルカリ処理及
び硫化処理して重金属水酸化物及び重金属硫化物を沈澱
分離せしめ、次いで該重金属水酸化物及び重金属硫化物
に上記残渣の一部と融剤とを加えて溶融固化することを
特徴とするものである。
Further, in the present invention, electrostatically precipitated ash is pickled to separate it into a residue and a solution containing heavy metal ions, and then the solution is treated with alkali and sulfurized to precipitate and separate heavy metal hydroxides and heavy metal sulfides. The method is characterized in that a part of the above residue and a flux are added to the heavy metal hydroxide and heavy metal sulfide and then melted and solidified.

又本発明は、酸洗処理が、溶解水を電気集塵灰に対して
0.踵量部以上加えて、その溶液をPH4.O〜6.5
としておこなうことを特徴とするものである。
In addition, in the present invention, the pickling treatment removes dissolved water from the electrostatically precipitated ash by 0.00%. Add more than the heel amount and adjust the solution to pH 4. O~6.5
It is characterized by the fact that it is carried out as follows.

又本発明はアルカリ処理を、PH9.5〜11.5でお
こなうことを特徴とするものである。
Further, the present invention is characterized in that the alkali treatment is carried out at a pH of 9.5 to 11.5.

又本発明は、重金属水酸化物の溶融固化を、重金属水酸
化物1重量部に対し残渣0.5〜5.0重量部、融剤0
.1〜1.0重量部を加えて、900〜1100℃で加
熱することを特徴とするものである。
In addition, the present invention melts and solidifies the heavy metal hydroxide with a residue of 0.5 to 5.0 parts by weight and 0 fluxing agent per 1 part by weight of the heavy metal hydroxide.
.. It is characterized by adding 1 to 1.0 parts by weight and heating at 900 to 1100°C.

又本発明は、重金属水酸化物及び重金属硫化物の溶融固
化を重金属水酸化物及び重金属硫化物1重量部に対し、
残渣0.5〜5.踵量部、融剤0.1〜1.濾量部を加
えて、900〜1100℃で加熱することを特徴とする
ものである。
In addition, the present invention provides melting and solidification of heavy metal hydroxides and heavy metal sulfides to 1 part by weight of heavy metal hydroxides and heavy metal sulfides.
Residue 0.5-5. Heel weight part, flux 0.1-1. It is characterized by adding a filtration part and heating at 900 to 1100°C.

以下本発明方法を第2図を参照して詳細に説明する。The method of the present invention will be explained in detail below with reference to FIG.

ます電気集塵灰21を酸洗処理して残渣22と重金属イ
オンを含む溶液23とに分離する。
The electrostatic precipitated ash 21 is pickled and separated into a residue 22 and a solution 23 containing heavy metal ions.

電気集塵灰21は、ごみ焼却炉等の電気集塵機から排出
されるもので、その化学組成は前述した第1表に示すよ
うに多くの重金属を含んでいる。酸洗処理は、ベルトコ
ンベア等の残渣掻上げ機24及び攪拌機25を備え予じ
め所定の組成に調合された溶解液で充された抽出槽26
内でおこない、ここに電気集塵灰21とともに塩酸溶液
等の溶解水27を入れ、これらを攪拌機25で攪拌する
ことによりおこなう。ここで溶解液の組成はほとんど変
動しない。溶解水27を入れることにより電気集塵灰2
1中の少量の重金属塩化物及び多量のアルカリ塩化物が
溶解する。この場合溶解水27の投入量は、電気集塵灰
21に含まれる塩化物を溶解した場合に、その溶液中の
塩化物濃度が飽和(30重量%程度)に近くなるような
割合で加えるのが望ましい。この理由は、後の廃液量を
できるだけ少なくするためにその投入量を最小限とする
のが好適であるからである。例えば電気集塵灰211重
量部に対して0.種量部以上加えて、その溶液をPH4
.O〜6.5とする。酸洗処理後の残渣22は、ベルト
コンベア24で運ばれ、洗浄水28で洗浄後貯溜槽29
に投入される。
The electrostatic precipitated ash 21 is discharged from an electrostatic precipitator such as a garbage incinerator, and its chemical composition includes many heavy metals as shown in Table 1 above. The pickling process is carried out in an extraction tank 26 equipped with a residue scraper 24 such as a belt conveyor and a stirrer 25 and filled with a solution prepared in advance to have a predetermined composition.
The electrostatic precipitated ash 21 and dissolved water 27 such as a hydrochloric acid solution are put therein, and the mixture is stirred with a stirrer 25. Here, the composition of the solution hardly changes. By adding dissolved water 27, electrostatically collected ash 2
A small amount of heavy metal chloride and a large amount of alkali chloride in 1 are dissolved. In this case, the amount of dissolved water 27 to be added is such that when the chloride contained in the electrostatically precipitated ash 21 is dissolved, the chloride concentration in the solution is close to saturation (approximately 30% by weight). is desirable. The reason for this is that it is preferable to minimize the input amount in order to minimize the subsequent amount of waste liquid. For example, 0.00% for 211 parts by weight of electrostatically collected ash. Add at least a seed amount and adjust the solution to PH4.
.. O to 6.5. The residue 22 after the pickling treatment is carried by a belt conveyor 24 and washed with washing water 28, and then transferred to a storage tank 29.
will be put into the

一方重金属イオンを含む溶液23は、ポンプ30で沈澱
槽31に送られアルカリ処理される。
On the other hand, the solution 23 containing heavy metal ions is sent to a precipitation tank 31 by a pump 30 and subjected to alkali treatment.

アルカリ処理は、沈澱槽31に水酸化ナトリウム32を
投入し、攪拌機33で攪拌することによりなされ、この
処理により重金属イオンが重金属水酸化物となつて沈澱
する。ここで最も沈澱しやすいPHは10.5であり、
このため槽内がPH9.5〜11.5の範囲となるよう
に水酸化ナトリウム32を投入するのが好適である。ま
た本発明は、上述したアルカリ処理工程で重金属イオン
を十分沈澱物にできないときにはさらにその炉液につい
て硫化処理を施すのが望ましい。
The alkali treatment is performed by charging sodium hydroxide 32 into a precipitation tank 31 and stirring it with a stirrer 33, and by this treatment, heavy metal ions become heavy metal hydroxides and precipitate. The pH at which precipitation is most likely to occur is 10.5,
Therefore, it is preferable to add sodium hydroxide 32 so that the pH inside the tank is in the range of 9.5 to 11.5. Further, in the present invention, when heavy metal ions cannot be sufficiently precipitated in the alkali treatment step described above, it is desirable to further perform a sulfurization treatment on the furnace liquid.

硫化処理は、硫化槽34内にアルカリ処理後の溶液及び
沈澱物を流入させ、ここに硫化ナトリウム(Na2S)
35を投入して攪拌機36で攪拌することによりおこな
われ、この処理により残存している少量の重金属イオン
が重金属硫化物として沈澱させる。この処理後沈澱物を
含む溶液は、フィルタ37により、溶液38と重金属水
酸化物又はこれと重金属硫化物の混合物(以下重金属水
酸化物等39と称す)とに分離される。
In the sulfurization treatment, the solution and precipitate after the alkali treatment are flowed into the sulfurization tank 34, and sodium sulfide (Na2S) is added thereto.
35 and stirring with a stirrer 36, and this treatment causes a small amount of remaining heavy metal ions to precipitate as heavy metal sulfides. The solution containing the precipitate after this treatment is separated by a filter 37 into a solution 38 and heavy metal hydroxide or a mixture of this and heavy metal sulfide (hereinafter referred to as heavy metal hydroxide etc. 39).

溶液38は中和槽40に入り塩酸41で中和される。一
方重金属水酸化物等39は、水洗して NaCL,KCLの付着をおとし、これを乾燥後酸洗処
理で得られた残渣22の一部22″と融剤42とともに
混練機43で混練する。
The solution 38 enters a neutralization tank 40 and is neutralized with hydrochloric acid 41. On the other hand, the heavy metal hydroxide etc. 39 is washed with water to remove adhesion of NaCL and KCL, and after drying, it is kneaded in a kneader 43 with a portion 22'' of the residue 22 obtained by the pickling treatment and a flux 42.

残渣22はここに重金属水酸化物等39を固定するため
のもので、その混合割合は融剤のコスト等を考慮して重
金属水酸化物等1重量部に対し0.5〜5.呼量部が適
当である。また融剤42は、この混合物を溶融する際、
その温度を下げて重金属が蒸発しないようにするための
もので、その混合割合は重金属水酸化物等1重量部に対
し0.1〜1.0重量部が適当である。この融剤42と
しては無水ほう酸、無水りん酸などが好適である。重金
属水酸化物等39と残渣22″と融剤42との混練物は
、、溶融炉44で溶融され、重金属水酸化物等は酸化物
、硫化物の形態でガラス質又は結晶質のスラグ中に固定
される。
The residue 22 is for fixing the heavy metal hydroxide etc. 39 here, and the mixing ratio thereof is 0.5 to 5.0 parts by weight per 1 part by weight of the heavy metal hydroxide etc., considering the cost of the flux. The traffic volume part is appropriate. Further, when melting this mixture, the fluxing agent 42
This is to lower the temperature to prevent heavy metals from evaporating, and the appropriate mixing ratio is 0.1 to 1.0 parts by weight per 1 part by weight of heavy metal hydroxide, etc. Suitable examples of the flux 42 include boric anhydride and phosphoric anhydride. A mixture of heavy metal hydroxide etc. 39, residue 22'' and flux 42 is melted in a melting furnace 44, and the heavy metal hydroxide etc. is in the form of oxides and sulfides in glassy or crystalline slag. Fixed.

溶融炉44は混練物を溶融するものであるが、高温にな
ると重金属が蒸発するため、900〜1100Cで加熱
溶融する。溶融炉44としては高周波電気炉、ガスだき
加熱炉等一般的な炉が使用できる。この処理方法によれ
ば、有害な重金属をガラス質又は結晶質とした残渣中に
固定するので重金属の溶出を確実に防止でき、しかも重
金属は酸化物等溶出し難い形態となつているため、長期
的にみても安定している。
The melting furnace 44 is for melting the kneaded material, and since heavy metals evaporate at high temperatures, the kneaded material is heated and melted at 900 to 1100 C. As the melting furnace 44, a general furnace such as a high frequency electric furnace or a gas-fired heating furnace can be used. According to this treatment method, harmful heavy metals are fixed in a glassy or crystalline residue, so the elution of heavy metals can be reliably prevented, and since the heavy metals are in a form that is difficult to elute, such as oxides, it can be used for a long period of time. Overall, it's stable.

また重金属の固定化に使用しない残りの残渣は、重金属
の溶出濃度が低いのでこれを投棄することができる。こ
こに本発明の実施例につき説明する。
Further, the remaining residue that is not used for immobilizing heavy metals can be discarded because the eluted concentration of heavy metals is low. Examples of the present invention will now be described.

実施例 電気集塵灰4.0k9を溶解水2.4eと10N上CL
ll6mlで酸処理し、酒過分離する。
Example Electrostatic precipitated ash 4.0k9 dissolved in water 2.4e and 10N CL
Acid treatment with 6 ml of alcohol was carried out, and alcoholic acid separation was carried out.

残渣は2.8′の水で洗浄する。この際得る枦液は次の
同様な操作の溶解水に混ぜ循環使用する。この操作をく
り返し4回行なつて得たPH=6.0の戸液の合量17
.49eを溶解液として50eのポリ容器に充し抽出槽
とする。再度この中に新たな別の電気集塵灰4.0k9
を溶解水2.4e110N−HCLll6mlとともに
投入し30分間混合攪拌したのち、吸引枦過器で残渣と
重金属イオンを含む枦液に分離し、残渣は2.81?の
水で洗浄して含水残渣3.21k9を得た。この実験に
使用した電気集塵灰、及び5回目に得られた残渣の化学
組成を第3表に示す。次に重金属イオンを含む溶液19
.331を10N一NaOH4OmlでPH=10.5
にアルカリ処理して含水重金属水酸化物559gを得、
更に微量のNa2sて硫化処理し、このようにして得た
水酸化物、硫化物をPH=10.5の洗浄水2.11で
洗浄した。
The residue is washed with 2.8' water. The liquid obtained at this time is mixed with the dissolving water in the next similar operation and used for circulation. This operation was repeated 4 times, resulting in a total amount of 17 mL of liquid with pH=6.0.
.. A 50e plastic container is filled with 49e as a dissolving liquid to form an extraction tank. Another new electrostatic precipitated ash 4.0k9 in this again
was added together with 6ml of dissolved water 2.4e110N-HCL, mixed and stirred for 30 minutes, and then separated into a residue and a liquid containing heavy metal ions using a suction filter, and the residue was 2.81? of water to obtain a water-containing residue 3.21k9. Table 3 shows the chemical composition of the electrostatically precipitated ash used in this experiment and the residue obtained in the fifth experiment. Next, solution 19 containing heavy metal ions
.. 331 with 10N-NaOH4Oml pH=10.5
was treated with alkali to obtain 559 g of hydrated heavy metal hydroxide.
Further, sulfurization treatment was carried out using a trace amount of Na2s, and the hydroxide and sulfide thus obtained were washed with 2.11 parts of washing water having a pH of 10.5.

次いで乾燥した水酸化物等82.8fに対して上記の残
渣を乾燥し、その一部の165.6f及び融剤(無水ほ
う酸)41.4fを加えて(水酸化物等1重量部に対し
て残渣2重量部、融剤0.5重量部)V型ブレンダーで
1.m間混合操作を行なつた。これをアルミナルツボに
移し、電気式マツフル炉内で1000℃で1.0時間に
て溶融し、溶融スラグの冷却固形化物231fを得た。
水酸化物等の沈澱物、溶融スラグの冷却固形化物の化学
組成及びその固形化物に有害重金属(Cd,Pb,T−
Cr)が固定された割合を第3表に示す。上表中、固定
率は、溶融前に配合した重金属水酸化物と残渣および無
水ほう酸に含まれる有害重金属の総和を100とし、溶
融後に得たスラグ固形化物中の有害重金属の含有量を割
合で示したものである。
Next, the above residue was dried against 82.8f of dried hydroxide, etc., and 165.6f of a part thereof and 41.4f of a flux (anhydrous boric acid) were added (per 1 part by weight of hydroxide, etc.). (2 parts by weight of residue, 0.5 parts by weight of flux) in a V-type blender. A mixing operation was performed for m. This was transferred to an aluminum crucible and melted in an electric Matsufuru furnace at 1000° C. for 1.0 hour to obtain a cooled solidified product 231f of molten slag.
The chemical composition of precipitates such as hydroxides, the cooled solidification of molten slag, and the presence of harmful heavy metals (Cd, Pb, T-
Table 3 shows the fixed ratio of Cr). In the above table, the fixation rate is defined as the total amount of harmful heavy metals contained in the heavy metal hydroxide, residue, and anhydrous boric acid blended before melting as 100, and the content of harmful heavy metals in the solidified slag obtained after melting as a percentage. This is what is shown.

次に上述した方法で得られた酸洗処理後の残渣及び溶融
スラグの冷却固形化物につき、溶出試験を行ない、その
結果を第4表に示す。
Next, an elution test was conducted on the residue after the pickling treatment and the cooled solidified product of the molten slag obtained by the above-mentioned method, and the results are shown in Table 4.

上表から本発明方法で処理すれば残渣及び固形化物はい
ずれも埋立投棄規制値を十分満足できることが確認され
た。
From the table above, it was confirmed that both the residue and the solidified material could sufficiently satisfy the landfill disposal regulation values if treated by the method of the present invention.

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

第1図は、従来の電気集塵灰の処理方法を示す説明図、
第2図は本発明の一実施例を示す電気集塵灰の処理方法
を示す説明図である。 21・・・電気集塵灰、22・・・残渣、23・・・溶
液、26・・・抽出槽、31・・・沈澱槽、32・・・
水酸化ナトリウム、43・・・混練機、44・・・溶融
炉。
FIG. 1 is an explanatory diagram showing a conventional method for processing electrostatically collected ash;
FIG. 2 is an explanatory diagram showing a method for treating electrostatically collected ash according to an embodiment of the present invention. 21... Electrostatic precipitated ash, 22... Residue, 23... Solution, 26... Extraction tank, 31... Sedimentation tank, 32...
Sodium hydroxide, 43...kneader, 44...melting furnace.

Claims (1)

【特許請求の範囲】 1 電気集塵灰を酸性処理して残渣と重金属イオンを含
む溶液とに分離した後該溶液をアルカリ処理して重金属
の水酸化物を沈殿分離せしめ、次いで該重金属の水酸化
物に上記残渣の一部と融剤とを加えて900〜1100
℃で加熱溶融固化することを特徴とする電気集塵灰の処
理方法。 2 酸性処理は、溶解液を電気集塵灰に対して0.7重
量部以上加えて、その溶液をPH4.0〜6.5とする
ことを特徴とする特許請求の範囲第1項記載の電気集塵
灰の処理方法。 3 アルカリ処理は、PH9.5〜11.5でおこなう
ことを特徴とする特許請求の範囲第1項記載の電気集塵
灰の処理方法。 4 重金属水酸化物の溶融固化は、重金属水酸化物1重
量部の対し、残渣0.5〜5.0重量部、融剤0.1〜
1.0重量部を加えて、900〜1100℃で加熱する
ことを特徴とする特許請求の範囲第1項記載の電気集塵
灰の処理方法。 5 電気集塵灰を酸洗処理して残渣と重金属イオンを含
む溶液とに分離した後該溶液をアルカリ処理及び硫化処
理して重金属水酸化物及び重金属硫化物を沈殿分離せし
め、次いで該重金属水酸化物及び重金属硫化物に上記残
渣の一部と融剤とを加えて90〜1100℃で加熱溶融
固化することを特徴とする電気集塵灰の処理方法。 6 酸洗処理は、溶解液を電気集塵灰に対して0.7重
量部以上加えて、その溶液をPH4.0〜6.5とする
ことを特徴とする特許請求の範囲第5項記載の電気集塵
灰の処理方法。 7 アルカリ処理は、PH9.5〜11.5でおこなう
ことを特徴とする特許請求の範囲第5項記載の電気集塵
灰の処理方法。 8 重金属水酸化物及び重金属硫化物の溶融固化は、重
金属水酸化物及び重金属硫化物1重量部に対し、残渣0
.5〜5.0重量部、融剤0.1〜1.0重量部を加え
て、900〜1100℃で加熱することを特徴とする特
許請求の範囲第5項記載の電気集塵灰の処理方法。
[Scope of Claims] 1 Electrostatically precipitated ash is treated with acid to separate it into a residue and a solution containing heavy metal ions, and then the solution is treated with alkali to precipitate and separate the hydroxides of heavy metals, and then the water of the heavy metals is separated. A part of the above residue and a flux are added to the oxide to give a powder of 900 to 1100.
A method for treating electrostatically precipitated ash, which is characterized by heating, melting, and solidifying at ℃. 2. The acidic treatment is performed by adding 0.7 parts by weight or more of a dissolving solution to electrostatically precipitated ash to adjust the pH of the solution to 4.0 to 6.5. Method of processing electrostatically collected ash. 3. The method for treating electrostatically precipitated ash according to claim 1, wherein the alkali treatment is carried out at a pH of 9.5 to 11.5. 4. In melting and solidifying the heavy metal hydroxide, 0.5 to 5.0 parts by weight of the residue and 0.1 to 0.1 parts by weight of the flux are used for 1 part by weight of the heavy metal hydroxide.
2. The method for treating electrostatically precipitated ash according to claim 1, wherein 1.0 part by weight is added and heated at 900 to 1100°C. 5 After the electrostatically precipitated ash is pickled and separated into a residue and a solution containing heavy metal ions, the solution is treated with alkali and sulfurized to precipitate and separate heavy metal hydroxides and heavy metal sulfides, and then the heavy metal water is separated. A method for treating electrostatically precipitated ash, which comprises adding a part of the above residue and a flux to oxides and heavy metal sulfides, and heating and melting and solidifying the mixture at 90 to 1100°C. 6. According to claim 5, the pickling treatment is performed by adding 0.7 parts by weight or more of a dissolving solution to the electrostatically collected ash to adjust the pH of the solution to 4.0 to 6.5. How to dispose of electrostatically collected ash. 7. The method for treating electrostatically precipitated ash according to claim 5, wherein the alkali treatment is carried out at a pH of 9.5 to 11.5. 8 The melting and solidification of heavy metal hydroxides and heavy metal sulfides produces 0 residue per 1 part by weight of heavy metal hydroxides and heavy metal sulfides.
.. 5 to 5.0 parts by weight and 0.1 to 1.0 parts by weight of a flux are added, and the electrostatically collected ash is heated at 900 to 1100°C. Method.
JP55073904A 1980-06-02 1980-06-02 How to dispose of electrostatically collected ash Expired JPS6052876B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55073904A JPS6052876B2 (en) 1980-06-02 1980-06-02 How to dispose of electrostatically collected ash

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55073904A JPS6052876B2 (en) 1980-06-02 1980-06-02 How to dispose of electrostatically collected ash

Publications (2)

Publication Number Publication Date
JPS56168873A JPS56168873A (en) 1981-12-25
JPS6052876B2 true JPS6052876B2 (en) 1985-11-21

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ID=13531636

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55073904A Expired JPS6052876B2 (en) 1980-06-02 1980-06-02 How to dispose of electrostatically collected ash

Country Status (1)

Country Link
JP (1) JPS6052876B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018148870A1 (en) * 2017-02-14 2018-08-23 深圳市能源环保有限公司 In-line heavy metal detection and solid waste dehazardization method
CN111040819B (en) * 2018-10-12 2021-08-20 国家能源投资集团有限责任公司 A kind of ash removal method of solid carbonaceous material

Also Published As

Publication number Publication date
JPS56168873A (en) 1981-12-25

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