JPH06246130A - Treatment of incinerator waste gas - Google Patents

Treatment of incinerator waste gas

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Publication number
JPH06246130A
JPH06246130A JP5056509A JP5650993A JPH06246130A JP H06246130 A JPH06246130 A JP H06246130A JP 5056509 A JP5056509 A JP 5056509A JP 5650993 A JP5650993 A JP 5650993A JP H06246130 A JPH06246130 A JP H06246130A
Authority
JP
Japan
Prior art keywords
magnesium hydroxide
hydrogen chloride
liquid
waste gas
tower
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.)
Granted
Application number
JP5056509A
Other languages
Japanese (ja)
Other versions
JP2592760B2 (en
Inventor
Hideo Matsui
英男 松井
Hiroaki Iimura
寛昭 飯村
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.)
KUREHA KANKYO KK
Original Assignee
KUREHA KANKYO KK
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 KUREHA KANKYO KK filed Critical KUREHA KANKYO KK
Priority to JP5056509A priority Critical patent/JP2592760B2/en
Publication of JPH06246130A publication Critical patent/JPH06246130A/en
Application granted granted Critical
Publication of JP2592760B2 publication Critical patent/JP2592760B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Treating Waste Gases (AREA)

Abstract

PURPOSE:To effectively absorb gaseous SO2 by making the difference in the concentration of magnesium hydroxide in a liquid absorbent between a process where hydrogen chloride is absorbed and removed and a process where gaseous SO2 is absorbed and removed. CONSTITUTION:After waste gas from an incinerator 9 is cooled in a quenching tower 1, it is brought into contact with a liquid absorbent contg. magnesium hydroxide in a hydrogen chloride absorber 2 to absorb and remove almost all hydrogen chloride. The absorbent at that time is adjusted so that liquid leaving the absorber 2 may have pH 3-5.5 by adding magnesium hydroxide to the supernatant in a supernatant tank 7 in mid-way of a suction line. Waste gas from which almost all hydrogen chloride has been removed is fed into a gaseous SO2 absorber 3, where when the absorbent adjusted so that liquid leaving the absorber 3 may have pH 5-7 by adding magnesium hydroxide to the supernatant in the supernatant tank 7 is sprayed to the top of the absorber 3, gaseous SO2 is absorbed and removed. Then the liquid is fed to a sedimentation tank 6, where smoke dust is settled.

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、廃棄物焼却炉廃ガスの
処理方法に関する。
FIELD OF THE INVENTION The present invention relates to a method for treating waste gas from a waste incinerator.

【0002】[0002]

【従来の技術】都市ごみあるいは産業廃棄物などを焼却
処理する場合に出る焼却炉廃ガスに含まれる塩化水素、
亜硫酸ガスなどを洗浄処理することが要求されている。
従来、このような塩化水素と亜硫酸ガスとを含む廃ガス
を無害化処理する場合には、水酸化ナトリウムが用いら
れていたが、水酸化ナトリウムが高価であることから安
価な水酸化マグネシウムを用いる方法が検討されてい
る。しかし、高濃度に塩化水素を含む廃ガスを洗浄処理
する場合に水酸化マグネシウムを使用すると亜硫酸ガス
の除去が効果的に行えない。このようなことから水酸化
マグネシウムと水酸化ナトリウムとを併用し、まず水酸
化マグネシウムで主として塩化水素を除去し、つづいて
水酸化ナトリウムで亜硫酸ガスを除去する方法が提案さ
れている(特開昭63-242322 号公報)。
2. Description of the Related Art Hydrogen chloride contained in incinerator waste gas generated when incinerating municipal waste or industrial waste,
Cleaning treatment with sulfurous acid gas is required.
Conventionally, sodium hydroxide was used when detoxifying waste gas containing such hydrogen chloride and sulfurous acid gas, but inexpensive magnesium hydroxide is used because sodium hydroxide is expensive. Methods are being considered. However, if magnesium hydroxide is used for cleaning the waste gas containing hydrogen chloride at a high concentration, the sulfurous acid gas cannot be effectively removed. For this reason, a method has been proposed in which magnesium hydroxide and sodium hydroxide are used in combination, firstly hydrogen chloride is mainly removed with magnesium hydroxide, and then sulfurous acid gas is removed with sodium hydroxide (Japanese Patent Laid-Open Publication No. S60-187242). 63-242322).

【0003】[0003]

【発明が解決しようとする課題】上述のように高濃度に
塩化水素を含む廃ガス処理を吸収剤として水酸化マグネ
シウムのみでは効率よく経済的に行い得ず、水酸化ナト
リウムまたは水酸化マグネシウムと水酸化ナトリウムを
併用しているのが現状である。しかし、高価な水酸化ナ
トリウムを使用せず、吸収剤として水酸化マグネシウム
のみを用いる廃ガス処理方法が望まれている。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention As described above, the treatment of waste gas containing hydrogen chloride at a high concentration as an absorbent cannot be performed efficiently and economically with magnesium hydroxide alone. The current situation is to use sodium oxide together. However, a waste gas treatment method using only magnesium hydroxide as an absorbent without using expensive sodium hydroxide is desired.

【0004】[0004]

【課題を解決するための手段】本発明者等は、水酸化マ
グネシウムを吸収剤とする廃ガス処理について鋭意研究
した結果、主として塩化水素を吸収除去する工程と主と
して亜硫酸ガスを吸収除去する工程とで、吸収液中の水
酸化マグネシウム濃度を異ならしめpHの異なる吸収液
を用いる本発明に到達した。即ち、本発明は、煤塵や酸
性物質を含む焼却炉廃ガスを水酸化マグネシウムを含む
吸収液で処理して塩化水素および亜硫酸ガスを吸収除去
するに当たり、塩化水素吸収塔での出口液pHが3〜
5.5になるように水酸化マグネシウムの入り口濃度が
調整された吸収液に接触させ主として塩化水素を吸収除
去する工程、つづいて亜硫酸ガス塔での出口液pHが5
〜7になるように水酸化マグネシウムの入り口濃度が調
整された吸収液と接触させて主として亜硫酸ガスを吸収
除去する工程、ガス接触後の両吸収液を混合静置して煤
塵を沈降分離する工程、および煤塵を分離した上澄液は
各吸収工程に循環させ、それぞれの過程で前記所定の入
り口濃度になるように水酸化マグネシウムを添加して濃
度を調整する工程よりなる焼却炉廃ガスの処理方法であ
る。
Means for Solving the Problems As a result of earnest studies on the treatment of waste gas using magnesium hydroxide as an absorbent, the present inventors have found that a process of absorbing and removing mainly hydrogen chloride and a process of absorbing and removing mainly sulfurous acid gas are performed. Thus, the present invention has been accomplished in which the concentration of magnesium hydroxide in the absorbing solution is varied and the absorbing solutions having different pH are used. That is, according to the present invention, when incinerator waste gas containing soot dust and acidic substances is treated with an absorption liquid containing magnesium hydroxide to absorb and remove hydrogen chloride and sulfur dioxide, the pH of the outlet liquid in the hydrogen chloride absorption tower is 3%. ~
A step of contacting with an absorbing solution whose inlet concentration of magnesium hydroxide is adjusted to 5.5 so as to mainly absorb and remove hydrogen chloride, and then the pH of the outlet solution in the sulfurous acid gas column is 5
A step of contacting with an absorbing solution whose magnesium hydroxide inlet concentration is adjusted to be ~ 7 to absorb and remove mainly sulfurous acid gas, and a step of mixing and leaving both absorbing solutions after gas contact to settle and separate soot dust , And the supernatant liquid from which soot and dust are separated is circulated to each absorption step, and in each step, magnesium hydroxide is added so that the predetermined inlet concentration is obtained and the concentration is adjusted to treat the incinerator waste gas. Is the way.

【0005】廃ガスに含まれる塩化水素、亜硫酸ガスは
水酸化マグネシウムを含む液と接触させるとき次式のよ
うに反応して吸収除去される。 Mg(OH)2 + 2HCl → MgCl2
2H2 O Mg(OH)2 + SO2 + 1/2O2 → M
gSO4 + H2 O しかし、産業廃棄物などの焼却炉廃ガスは、通常、亜硫
酸ガス50〜800ppm 、塩化水素400〜4000pp
m を含むほか、多量の煤塵を含んでいる。このような廃
ガスを水酸化マグネシウムスラリーと接触させるとき
は、塩化水素は殆ど吸収除去されるが、亜硫酸ガスは余
り吸収されない。これは水酸化マグネシウムの溶解度が
極めて小さいことと焼却炉廃ガスには亜硫酸ガスに比べ
多量の塩化水素が含まれているためである。このため、
本発明では、主として塩化水素を吸収する工程と主とし
て亜硫酸ガスを吸収する工程を分け、循環する吸収液を
各工程で水酸化マグネシウムの濃度を異ならしめること
により、亜硫酸ガスの吸収を効率よく吸収除去する。
Hydrogen chloride and sulfurous acid gas contained in the waste gas are absorbed and removed by reacting as shown in the following equation when brought into contact with a liquid containing magnesium hydroxide. Mg (OH) 2 + 2HCl → MgCl 2 +
2H 2 O Mg (OH) 2 + SO 2 + 1 / 2O 2 → M
gSO 4 + H 2 O However, the incinerator waste gas such as industrial waste is usually 50 to 800 ppm of sulfurous acid gas, 400 to 4000 pp of hydrogen chloride.
In addition to m, it contains a large amount of dust. When such waste gas is brought into contact with the magnesium hydroxide slurry, most of the hydrogen chloride is absorbed and removed, but the sulfurous acid gas is hardly absorbed. This is because the solubility of magnesium hydroxide is extremely small and the incinerator waste gas contains a large amount of hydrogen chloride as compared with sulfurous acid gas. For this reason,
In the present invention, the step of mainly absorbing hydrogen chloride and the step of mainly absorbing sulfurous acid gas are separated, and the concentration of magnesium hydroxide is changed in each step of the circulating absorption liquid, whereby the absorption of sulfurous acid gas is efficiently absorbed and removed. To do.

【0006】以下、図1により本発明を詳しく説明す
る。図1において、1は急冷塔、2は塩化水素吸収塔、
3は亜硫酸ガス吸収塔で、各塔の下部には吸収液排出管
が、塔上部には吸収液導入管が接続されており、焼却炉
4からの廃ガスは各塔でスプレーノズルから散布される
降下液(吸収液)と順次接触し浄化され、更に集塵機を
経て清浄ガスとして排出される。焼却炉4からの廃ガス
は急冷塔1で100℃以下好ましくは80℃程度にまで
冷却するが、このとき急冷塔に水酸化マグネシウムを含
む液のヌレ壁を形成させるのが好ましい。このとき廃ガ
ス中の塩化水素の一部は吸収され、この吸収液は混合槽
5に送られる。急冷塔出廃ガスは、塩化水素吸収塔2で
水酸化マグネシウムを含む吸収液と接触して塩化水素の
殆ど全部が吸収除去される。塩化水素吸収塔2にスプレ
ーされる吸収液は、上澄液槽7の上澄み液に水酸化マグ
ネシウムを吸入ライン中で添加して塔2出口液pHが3
〜5.5なるように調整する。この濃度調整は、塔2出
口液のpHを連続的に検出し、廃ガス中の塩化水素濃度
の変動に追従させながら、塔出口液pHが上記範囲内に
なるよう、水酸化マグネシウムの添加を行う。塔2への
供給液の水酸化マグネシウム濃度は廃ガス中の酸成分の
濃度、吸収塔におけるガス/液比等により異なるが、通
常水酸化マグネシウムが0.01〜0.15重量%の液
である。塔2の出口液も混合槽5に送られる。
The present invention will be described in detail below with reference to FIG. In FIG. 1, 1 is a quenching tower, 2 is a hydrogen chloride absorption tower,
Reference numeral 3 is a sulfur dioxide absorption tower, an absorption liquid discharge pipe is connected to the lower part of each tower, and an absorption liquid introduction pipe is connected to the upper part of the tower. Waste gas from the incinerator 4 is sprayed from the spray nozzle in each tower. It is sequentially contacted with the falling liquid (absorption liquid) and purified, and then discharged as a clean gas through a dust collector. The waste gas from the incinerator 4 is cooled in the quenching tower 1 to 100 ° C. or less, preferably about 80 ° C. At this time, it is preferable to form a wetting wall of a liquid containing magnesium hydroxide in the quenching tower. At this time, a part of hydrogen chloride in the waste gas is absorbed, and this absorption liquid is sent to the mixing tank 5. The waste gas discharged from the quenching tower comes into contact with the absorbing solution containing magnesium hydroxide in the hydrogen chloride absorption tower 2 so that almost all of hydrogen chloride is absorbed and removed. The absorption liquid sprayed to the hydrogen chloride absorption tower 2 is obtained by adding magnesium hydroxide to the supernatant liquid of the supernatant liquid tank 7 in the suction line so that the outlet liquid pH of the tower 2 is 3
Adjust to be ~ 5.5. This concentration adjustment is performed by continuously detecting the pH of the outlet liquid of the tower 2 and adding magnesium hydroxide so that the pH of the outlet liquid of the tower is within the above range while following the fluctuation of the concentration of hydrogen chloride in the waste gas. To do. The magnesium hydroxide concentration of the liquid supplied to the tower 2 varies depending on the concentration of the acid component in the waste gas, the gas / liquid ratio in the absorption tower, etc. is there. The outlet liquid of the tower 2 is also sent to the mixing tank 5.

【0007】なお、急冷塔において出液量が多い場合に
は、この出液のpHを検出するべく、塩化水素吸収塔供
給液と同様に、上澄液槽7の液に水酸化マグネシウムを
補給調整した液を冷却水として用いることもできる。塩
化水素が略除去された廃ガスは亜硫酸ガス吸収塔3に送
られ、ここでも上澄液槽7の上澄み液に水酸化マグネシ
ウムを吸入ライン中で添加して塔出口液pHが5〜7に
なる濃度に調製された吸収液が塔頂からスプレーされ、
亜硫酸ガスが吸収除去される。塔3に供給される吸収液
の水酸化マグネシウム濃度は、塔2の場合と同様に、塔
3の出口液のpHを連続的に検出することにより行われ
る。塔3の出口液も混合槽5に送られる。
When the amount of liquid discharged in the quenching tower is large, magnesium hydroxide is replenished to the liquid in the supernatant liquid tank 7 in the same manner as the hydrogen chloride absorption tower supply liquid in order to detect the pH of the liquid discharged. The prepared liquid can also be used as cooling water. The waste gas from which hydrogen chloride has been substantially removed is sent to the sulfurous acid gas absorption tower 3, and here also magnesium hydroxide is added to the supernatant of the supernatant tank 7 in the suction line to adjust the pH of the tower outlet liquid to 5-7. The absorption liquid prepared to have the following concentration is sprayed from the top of the tower,
Sulfurous acid gas is absorbed and removed. The magnesium hydroxide concentration of the absorption liquid supplied to the tower 3 is determined by continuously detecting the pH of the outlet liquid of the tower 3, as in the case of the tower 2. The outlet liquid of the tower 3 is also sent to the mixing tank 5.

【0008】塔3で亜硫酸ガスを充分に吸収除去するた
めには、塔3出口液のpHは5〜7にあることが必要で
あり、塔2出口液のpHが5.5をこえると未反応水酸
化マグネシウム含有量が多くなり、沈降槽6での沈降ロ
スが多くなる。混合槽5では、各塔からの未反応酸成分
および水酸化マグネシウムを含むpHの異なる出液を混
合反応させ、静置沈降槽6に送られ、静置して煤塵を沈
降させる。静置沈降槽の上澄み液は上澄液槽7に送ら
れ、槽底部に溜まる沈降物はスラリー状で取り出され排
水処理工程に送られ処理される。なお、混合槽と静置沈
降槽は一つの槽を連通孔を有する仕切り板で仕切った構
造であってもよい。上澄液槽7では、沈降槽で抜きだし
た水および蒸発水量に相当する量の水を補給され、それ
ぞれの吸入ラインで水酸化マグネシウムを添加されなが
ら各吸収塔に循環される。
In order to sufficiently absorb and remove the sulfurous acid gas in the tower 3, the pH of the outlet liquid of the tower 3 must be 5 to 7, and when the pH of the outlet liquid of the tower 2 exceeds 5.5, it is not possible. The reaction magnesium hydroxide content increases, and the sedimentation loss in the sedimentation tank 6 increases. In the mixing tank 5, the unreacted acid component from each tower and the effluent containing magnesium hydroxide having different pHs are mixed and reacted, and sent to the stationary settling tank 6 where they are allowed to stand to precipitate the soot dust. The supernatant of the stationary settling tank is sent to the supernatant tank 7, and the sediment accumulated at the bottom of the tank is taken out in the form of slurry and sent to the wastewater treatment step for treatment. The mixing tank and the stationary settling tank may have a structure in which one tank is partitioned by a partition plate having a communication hole. In the supernatant liquid tank 7, water extracted in the sedimentation tank and water in an amount corresponding to the amount of evaporated water are replenished, and magnesium hydroxide is circulated in each absorption tower while magnesium hydroxide is added in each suction line.

【0009】本発明では、上澄液槽7の上澄み液を吸収
液として吸収塔に循環させるに当たり、上記した塩酸吸
収塔2への供給液の濃度調整は、この上澄み液のpHと
塔2の出口液のpHとを検出しながら該出口液のpHが
3〜5.5になる量(Mg(OH)20.1〜1.5g/l)の水酸化マ
グネシウムを添加する。また亜硫酸ガス吸収塔への供給
液の濃度調整は、亜硫酸ガス吸収塔出口液のpHを検出
しながら該塔出口液pHが5〜7、好ましくは6〜6.
5に維持される量の水酸化マグネシウム(Mg(OH)2 0.02
〜0.5g/l)を前記上澄み液に添加して行う。亜硫酸ガス
吸収塔出口液pHが5以下になると亜硫酸ガスを充分に
吸収除去できない。主として塩化水素を吸収する工程と
主として亜硫酸ガスを吸収する工程に分け、上記したよ
うに吸収液のpHを調整するときは、吸収剤が水酸化マ
グネシウム単独であっても塩化水素を30ppm以下
に、亜硫酸ガスを5ppm以下にまで除去することがで
きる。本発明の方法は、産業廃棄物および一般廃棄物等
の焼却炉処理に用いられる。
In the present invention, when the supernatant liquid of the supernatant liquid tank 7 is circulated in the absorption tower as the absorption liquid, the concentration of the liquid supply to the hydrochloric acid absorption tower 2 is adjusted by adjusting the pH of the supernatant liquid and the tower 2. While detecting the pH of the outlet liquid, magnesium hydroxide in an amount such that the pH of the outlet liquid becomes 3 to 5.5 (Mg (OH) 2 0.1 to 1.5 g / l) is added. The concentration of the liquid supplied to the sulfur dioxide absorption tower is adjusted while the pH of the sulfur dioxide absorption tower outlet liquid is being detected while the tower outlet liquid pH is 5 to 7, preferably 6 to 6.
The amount of magnesium hydroxide (Mg (OH) 2 0.02
˜0.5 g / l) is added to the above supernatant. When the pH of the solution at the outlet of the sulfurous acid gas absorption tower becomes 5 or less, the sulfurous acid gas cannot be sufficiently absorbed and removed. When the pH of the absorbing solution is adjusted as described above by dividing it into a step of mainly absorbing hydrogen chloride and a step of mainly absorbing sulfur dioxide, hydrogen chloride is adjusted to 30 ppm or less even if the absorbent is magnesium hydroxide alone. Sulfurous acid gas can be removed to 5 ppm or less. The method of the present invention is used for incinerator treatment of industrial waste, general waste, and the like.

【0010】[0010]

【実施例】主として塩化ビニル樹脂を含む廃棄物を焼却
して発生する廃ガスを図1に示すような装置を用いて処
理した。急冷塔1で冷却した廃ガス(塩化水素:2000〜
2400ppm 、亜硫酸ガス:70〜90ppm 、煤塵 6g/Nm3
有)40000 〜50000 Nm3/H を吸収塔2及び3に順次導入
した。塩酸吸収塔2では沈降槽上澄み液に水酸化マグネ
シウムを添加した液(pH9.3 、Mg(OH)2 0.06%)を300m
3/H スプレーした。亜硫酸ガス吸収塔3では沈降槽上澄
み液に水酸化マグネシウムを添加した液(pH9.0 、Mg
(OH)2 0.005%)を300m3/H スプレーした。亜硫酸ガス吸
収塔出口液のpHは6.0 〜6.2 にコントロールされた。
また塩化水素吸収塔出口液のpHは4.2 〜4.5 であっ
た。なお、吸収液と接触後のガス中の塩化水素は20 pp
m, 亜硫酸ガスは4 ppm であった。
EXAMPLE Waste gas generated by incineration of waste mainly containing vinyl chloride resin was treated using an apparatus as shown in FIG. Waste gas cooled in the quench tower 1 (hydrogen chloride: 2000-
2400 ppm, sulfurous acid gas: 70 to 90 ppm, containing 6 g / Nm 3 of dust) 40000 to 50000 Nm 3 / H were sequentially introduced into the absorption towers 2 and 3. In the hydrochloric acid absorption tower 2, 300m of liquid (pH 9.3, Mg (OH) 2 0.06%) in which magnesium hydroxide was added to the supernatant of the sedimentation tank was used.
3 / H sprayed. In the sulfurous acid gas absorption tower 3, a liquid obtained by adding magnesium hydroxide to the supernatant of the sedimentation tank (pH 9.0, Mg
(OH) 2 0.005%) was sprayed at 300 m 3 / H. The pH of the sulfur dioxide gas absorption tower outlet liquid was controlled at 6.0 to 6.2.
The pH of the hydrogen chloride absorption tower outlet liquid was 4.2 to 4.5. The hydrogen chloride content in the gas after contact with the absorbing liquid was 20 pp.
m, sulfurous acid gas was 4 ppm.

【0011】急冷塔1、塩化水素吸収塔2および亜硫酸
ガス吸収塔3の出口液は混合槽5に集め撹拌反応させて
静置沈降槽6に送った。静置沈降槽6での滞留時間は約
15分であった。これを上澄液槽7に貯留した。この上
澄み液のpHは5.5 〜5.8 であった。塩化水素吸収塔2
に循環する上澄み液および亜硫酸ガス吸収塔3に循環す
る上澄み液に添加した水酸化マグネシウムはそれぞれ濃
度150g/lであった。上澄み液に添加した水酸化マグネシ
ウム量は、それぞれ 157kg/Hおよび12kg/Hであった。な
お、水酸化マグネシウムの添加は約15重量%のスラリー
で行った。
The outlet liquids of the quenching tower 1, the hydrogen chloride absorption tower 2 and the sulfurous acid gas absorption tower 3 were collected in a mixing tank 5 and reacted with stirring to be sent to a stationary settling tank 6. The residence time in the stationary settling tank 6 was about 15 minutes. This was stored in the supernatant liquid tank 7. The pH of this supernatant was 5.5 to 5.8. Hydrogen chloride absorption tower 2
The concentration of magnesium hydroxide added to the supernatant liquid circulated in the above and that added to the supernatant liquid circulated in the sulfurous acid gas absorption tower 3 was 150 g / l, respectively. The amounts of magnesium hydroxide added to the supernatant were 157 kg / H and 12 kg / H, respectively. The magnesium hydroxide was added in a slurry of about 15% by weight.

【0012】[0012]

【発明の効果】上述のように、亜硫酸ガスおよび多量の
塩化水素を含む廃ガスを、主として塩化水素を吸収する
工程と主として亜硫酸ガスを吸収する工程とに分け、か
つ、その吸収液の液性を個別に調整する本発明方法によ
れば、吸収剤として水酸化マグネシウム単一使用するこ
とによって廃ガスを充分に清浄化することができる。ま
たこのようにすることにより、未反応水酸化マグネシウ
ムの損失も少なく、工業的有利な廃ガス処理方法であ
る。
As described above, the waste gas containing sulfurous acid gas and a large amount of hydrogen chloride is divided into the step of mainly absorbing hydrogen chloride and the step of mainly absorbing sulfurous acid gas, and the liquidity of the absorption liquid is increased. According to the method of the present invention for individually adjusting the above, the waste gas can be sufficiently cleaned by using magnesium hydroxide alone as the absorbent. Further, by doing so, there is little loss of unreacted magnesium hydroxide, and this is an industrially advantageous waste gas treatment method.

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

【図1】本発明の工程を示すフローシートである。FIG. 1 is a flow sheet showing the steps of the present invention.

【符号の説明】[Explanation of symbols]

1 急冷塔 2 塩化水素吸収塔 3 亜硫酸ガス吸収塔 4 焼却炉 5 混合槽 6 静置沈降槽 7 上澄液槽 1 Quenching tower 2 Hydrogen chloride absorption tower 3 Sulfurous acid gas absorption tower 4 Incinerator 5 Mixing tank 6 Stationary sedimentation tank 7 Supernatant tank

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 煤塵や酸性物質を含む焼却炉廃ガスを水
酸化マグネシウムを含む吸収液で処理して塩化水素およ
び亜硫酸ガスを吸収除去するに当たり、塩化水素吸収塔
での塔出口液pHが3〜5.5になるように水酸化マグ
ネシウムの入り口濃度が調整された吸収液に接触させ主
として塩化水素を吸収除去する工程、つづいて亜硫酸ガ
ス吸収塔で接触後のpHが5〜7になるように水酸化マ
グネシウムの入り口濃度が調整された吸収液と接触させ
て主として亜硫酸ガスを吸収除去する工程、ガス接触後
の両吸収液を混合静置して煤塵を沈降分離する工程、お
よび煤塵を分離した上澄液は各吸収工程に循環させ、そ
れぞれの過程で前記所定の入り口濃度になるように水酸
化マグネシウムを添加して濃度を調整する工程よりなる
ことを特徴とする焼却炉廃ガスの処理方法。
1. When the incinerator waste gas containing soot dust and acidic substances is treated with an absorbent containing magnesium hydroxide to absorb and remove hydrogen chloride and sulfur dioxide, the pH of the outlet liquid in the hydrogen chloride absorption tower is 3%. A step of contacting with an absorbing solution whose inlet concentration of magnesium hydroxide is adjusted to be about 5.5 to absorb and remove mainly hydrogen chloride, and then a pH of the mixture after contacting with a sulfurous acid gas absorption tower is 5 to 7 In order to absorb and remove mainly sulfurous acid gas by contacting it with an absorbing solution whose magnesium hydroxide inlet concentration is adjusted, after mixing the two absorbing solutions after gas contact, settling and separating soot and dust, and separating soot and dust The clarified supernatant liquid is circulated in each absorption step, and in each step, magnesium hydroxide is added so that the predetermined inlet concentration is obtained, and the concentration is adjusted. Incinerator waste gas treatment method.
JP5056509A 1993-02-22 1993-02-22 How to treat incinerator waste gas Expired - Fee Related JP2592760B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5056509A JP2592760B2 (en) 1993-02-22 1993-02-22 How to treat incinerator waste gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5056509A JP2592760B2 (en) 1993-02-22 1993-02-22 How to treat incinerator waste gas

Publications (2)

Publication Number Publication Date
JPH06246130A true JPH06246130A (en) 1994-09-06
JP2592760B2 JP2592760B2 (en) 1997-03-19

Family

ID=13029099

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5056509A Expired - Fee Related JP2592760B2 (en) 1993-02-22 1993-02-22 How to treat incinerator waste gas

Country Status (1)

Country Link
JP (1) JP2592760B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110090531A (en) * 2019-05-22 2019-08-06 中国石油集团东北炼化工程有限公司锦州设计院 A kind of efficient refinery's organic waste gas treatment device containing benzene and processing method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5057968A (en) * 1973-09-22 1975-05-20
JPH0380915A (en) * 1989-08-24 1991-04-05 Babcock Hitachi Kk Wet type flue gas desulfurization
JPH0478418A (en) * 1990-07-19 1992-03-12 Kenichi Nakagawa Method for desulfurizing waste gas
JPH04227818A (en) * 1990-04-18 1992-08-17 Metallges Ag Waste gas purification method

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5057968A (en) * 1973-09-22 1975-05-20
JPH0380915A (en) * 1989-08-24 1991-04-05 Babcock Hitachi Kk Wet type flue gas desulfurization
JPH04227818A (en) * 1990-04-18 1992-08-17 Metallges Ag Waste gas purification method
JPH0478418A (en) * 1990-07-19 1992-03-12 Kenichi Nakagawa Method for desulfurizing waste gas

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110090531A (en) * 2019-05-22 2019-08-06 中国石油集团东北炼化工程有限公司锦州设计院 A kind of efficient refinery's organic waste gas treatment device containing benzene and processing method

Also Published As

Publication number Publication date
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