JPH06170153A - Treatment of exhaust gas - Google Patents

Treatment of exhaust gas

Info

Publication number
JPH06170153A
JPH06170153A JP4350654A JP35065492A JPH06170153A JP H06170153 A JPH06170153 A JP H06170153A JP 4350654 A JP4350654 A JP 4350654A JP 35065492 A JP35065492 A JP 35065492A JP H06170153 A JPH06170153 A JP H06170153A
Authority
JP
Japan
Prior art keywords
exhaust gas
scrubber
scrubbers
treatment
desulfurizing agent
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.)
Pending
Application number
JP4350654A
Other languages
Japanese (ja)
Inventor
Kenichi Nakagawa
健一 中川
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP4350654A priority Critical patent/JPH06170153A/en
Publication of JPH06170153A publication Critical patent/JPH06170153A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide a method for treating exhaust gas economically and favorably in the case of performing dust removal and desulfurization treatment of exhaust gas in a scrubber by decreasing trouble of corrosion in a route of exhaust gas and avoiding trouble in loss of an alkali agent. CONSTITUTION:Dust removal and desulfurization are performed by introducing exhaust gas G into many pieces of scrubbers 1 (1A-1E) arranged in a row and bringing a processing solution containing a desulfurizing agent consisting of water and an alkali agent into contact therewith. In the case of leading exhaust gas G' derived from the respective scrubbers 1 (1A to 1E) to a stack 7 through the respective fans 5 (5A to 5E) and discharging it to the atmosphere, a treatment flow path 9 is formed by which the processing solutions of the respective scrubbers 1 (1A to 1E) are successively transferred to the adjacent scrubber sides. The whole amount of the desulfurizing agent necessary for the respective scrubbers is supplied to the initial scrubber 1A side in the treatment flow path 9. pH of the processing liquid in the final scrubber 1E side is regulated to about 6.

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、石炭燃焼ボイラ―など
から排出される排ガスの処理方法、詳しくは排ガス中に
含まれる灰分やSO2 などの硫黄酸化物を取り除く脱塵
および脱硫の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 treating exhaust gas discharged from a coal combustion boiler or the like, and more particularly to a method for dedusting and desulfurizing ash contained in exhaust gas and sulfur oxides such as SO 2. It is a thing.

【0002】[0002]

【従来の技術】この種の脱塵および脱硫は、通常この順
に行われることが多いが、設置場所や設備費などを考え
ると、同時に行うことが望ましい。同時処理の方法に
は、スクラツバ―内に導入した排ガスに、水およびアル
カリ試剤からなる脱硫剤を含む処理液を接触させて、排
ガス中の灰分を捕捉し、同時に硫黄酸化物をアルカリ試
剤と反応させて脱硫生成物として取り除く方法がある。
2. Description of the Related Art Dedusting and desulfurization of this type are usually carried out in this order, but it is desirable to carry out at the same time in consideration of the installation site and equipment costs. The simultaneous treatment method involves contacting the exhaust gas introduced into the scrubber with a treatment liquid containing a desulfurizing agent consisting of water and an alkaline reagent to capture the ash in the exhaust gas and simultaneously reacting sulfur oxides with the alkaline reagent. There is a method of removing it as a desulfurization product.

【0003】また、発電所などでは、多数のボイラ―を
同時に稼動しているため、各ボイラ―から排出される排
ガスは、それぞれ別個のスクラツバ―内で上述の如く脱
塵および脱硫処理され、これら排ガスを各送風機でひと
つの煙道にまとめ、1本の煙突から、大気中に放出する
ようにしている。
In a power plant and the like, a large number of boilers are operated at the same time, so the exhaust gas discharged from each boiler is dedusted and desulfurized as described above in separate scrubbers. The exhaust gas is collected by each blower into one flue and discharged into the atmosphere from one chimney.

【0004】ところで、このような排ガスの処理方法に
おいて、スクラツバ―内での脱硫反応は、脱硫剤がMg
(OH)2 の場合、つぎの(1),(2)式; Mg(OH)2 +SO2 +H2 O=MgSO3 +H2 O …(1) MgSO3 +SO2 +H2 O=Mg(HSO3 2 …(2) の反応が起こる。両反応は、処理液のPHに依存し、P
Hが低いと(2)式の反応が主となつてMg(HS
3 2 が多く生成し、PHが高いと(1)式の反応が
主となつてMgSO3 が多く生成する。したがつて、処
理液中のMgSO3 /Mg(HSO3 2 の比は、たと
えば、PH5.8で1/10、PH6.8で1/1、P
H7.8で10/1となる如くである。
By the way, in such an exhaust gas treating method, the desulfurization reaction in the scrubber is carried out by using the desulfurizing agent as Mg.
In the case of (OH) 2, the following formulas (1) and (2); Mg (OH) 2 + SO 2 + H 2 O = MgSO 3 + H 2 O (1) MgSO 3 + SO 2 + H 2 O = Mg (HSO 3 ) reaction of 2 ... (2) occurs. Both reactions depend on the pH of the treatment solution,
When H is low, the reaction of the formula (2) is mainly and Mg (HS
A large amount of O 3 ) 2 is produced, and when PH is high, the reaction of the formula (1) is mainly produced and a large amount of MgSO 3 is produced. Therefore, the ratio of MgSO 3 / Mg (HSO 3 ) 2 in the treatment liquid is, for example, 1/10 at PH 5.8, 1/1 at PH 6.8, P
It seems that it will be 10/1 at H7.8.

【0005】ここで、処理液のPHを上記の5.8に設
定すると、排ガスの排気経路に若干のミストが逸出した
とき、そのドレンが高濃度のMg(HSO3 2 を含む
液となり、これが排ガス中の酸素とつぎの(3)式; Mg(HSO3 2 +O2 =MgSO3 +H2 SO4 …(3) の反応を起こし、硫酸を生成する。その結果、ドレンの
PHは約2程度にまで降下し、排気経路の送風機や煙
道、煙突などを腐食する。このため、送風機などの材質
はステンレス製では持たず、高価な耐酸性材質にしなけ
ればならないし、煙道や煙突なども高価の耐酸性ライニ
ングを施す必要がある。
Here, if the pH of the treatment liquid is set to the above-mentioned 5.8, when some mist escapes to the exhaust path of the exhaust gas, the drain becomes a liquid containing a high concentration of Mg (HSO 3 ) 2. This causes the reaction of oxygen in the exhaust gas with the following formula (3); Mg (HSO 3 ) 2 + O 2 = MgSO 3 + H 2 SO 4 (3) to generate sulfuric acid. As a result, the pH of the drain drops to about 2 and corrodes the blower, flue, and chimney in the exhaust path. Therefore, the material of the blower and the like is not made of stainless steel but must be an expensive acid resistant material, and the flue and chimney must also be provided with an expensive acid resistant lining.

【0006】一方、処理液のPHを上記の7.8に設定
すると、排気経路におけるドレンはMgSO3 を多く含
んだものとなるため、上記(3)式の反応による硫酸の
生成には至らない。したがつて、送風機などの腐食の心
配がなく、ステンレス製などの安価な材質やライニング
にて対応できる。しかし、PHをこのように高くする
と、排ガス中に10〜15%程度も混在するCO2 と、
つぎの(4)式; Mg(OH)2 +2CO2 +H2 O =Mg(HCO3 2 +H2 O …(4) の反応を起こすことになり、この反応で生成した重炭酸
塩は、系外に排出されるため、脱硫剤のロスとなる。
On the other hand, if the pH of the treatment liquid is set to 7.8, the drain in the exhaust path contains a large amount of MgSO 3 , so that sulfuric acid is not produced by the reaction of the above formula (3). . Therefore, there is no concern about corrosion of the blower, etc., and it can be handled with inexpensive materials such as stainless steel and lining. However, if the PH is increased in this way, CO 2 mixed in the exhaust gas by about 10 to 15%,
The following formula (4): Mg (OH) 2 + 2CO 2 + H 2 O = Mg (HCO 3 ) 2 + H 2 O (4) will occur, and the bicarbonate produced by this reaction Since it is discharged to the outside, it becomes a loss of the desulfurizing agent.

【0007】一例として、排ガス中のSO2 の濃度を6
00ppm、CO2 濃度を10%としたとき、脱硫剤と
して用いる正味のMg(OH)2 に対して、排出重炭酸
塩としてのロスの割合は、PH6で約2%、PH6.3
で約4%、PH6.6で約8%、PH6.7で約10
%、PH7.0で約20%となる。したがつて、経済性
の点を考えると、上記のロスが約2〜4%程度となるP
H6〜6.3程度で処理するのが望ましいことになる
が、この場合は、既述のとおり、排気経路の送風機や煙
道、煙突などの腐食の問題が生じてくる。
As an example, the concentration of SO 2 in exhaust gas is set to 6
When the concentration of CO 2 is 00 ppm and the concentration of CO 2 is 10%, the ratio of the loss as the discharged bicarbonate is about 2% at PH6, and about 6.3% at PH6.3 with respect to the net Mg (OH) 2 used as the desulfurizing agent.
About 4%, PH 6.6 about 8%, PH 6.7 about 10
%, PH 7.0 is about 20%. Therefore, in terms of economic efficiency, the above loss is about 2-4% P
It is desirable to treat at about H6 to 6.3, but in this case, as described above, there arises a problem of corrosion of the blower of the exhaust path, the flue, the chimney, and the like.

【0008】なお、上記では、脱硫剤として、Mg(O
H)2 を用いた例で説明したが、その他CaO、Ca
(OH)2 などのMgやCaを含む化合物のほか、苛性
ソ―ダや苛性カリなどを用いる場合でも、ほぼ同じであ
り、脱硫剤としてアルカリ試剤を用いる以上、どうして
もさけられない問題である。
In the above, as the desulfurizing agent, Mg (O
H) 2 has been described as an example, but other CaO, Ca
This is almost the same when using compounds such as (OH) 2 containing Mg and Ca, as well as caustic soda and caustic potash, and this is an unavoidable problem as long as an alkaline reagent is used as a desulfurizing agent.

【0009】[0009]

【発明が解決しようとする課題】このように、スクラツ
バ―内で排ガスの脱塵および脱硫を行う従来の処理方法
においては、脱硫剤であるアルカリ試剤を少なめにして
処理液のPHを低く抑えると、スクラツバ―以降の排気
経路に腐食の問題を生じ、その対策に高価な耐酸性材質
などを用いる必要があるし、逆にアルカリ試剤を多めに
して処理液のPHを高く設定すると、アルカリ試剤のロ
スの問題を生じてくるというように、いずれも経済的に
不利とならざるを得なかつた。
As described above, in the conventional treatment method for dedusting and desulfurizing exhaust gas in the scrubber, if the alkaline reagent which is a desulfurizing agent is reduced and the pH of the treating solution is kept low. , The problem of corrosion occurs in the exhaust path after the scrubber, and it is necessary to use expensive acid-resistant materials etc. as a countermeasure against it, and conversely, if the amount of alkaline reagent is increased and the pH of the processing liquid is set high, All of them had to be economically disadvantageous, such as causing the problem of loss.

【0010】本発明は、上記の事情に鑑み、スクラツバ
―内で排ガスの脱塵および脱硫を行うにあたり、排気経
路での腐食の問題を軽減し、かつアルカリ試剤のロスの
問題を回避して、経済的に有利な処理方法を提供するこ
とを目的としている。
In view of the above circumstances, the present invention reduces the problem of corrosion in the exhaust passage when dedusting and desulfurizing exhaust gas in a scrubber, and avoids the problem of alkali reagent loss. The purpose is to provide an economically advantageous treatment method.

【0011】[0011]

【課題を解決するための手段】本発明者は、上記の目的
を達成するため、鋭意検討した結果、既述のように、発
電所などでは多数のボイラ―から排出される排ガスを別
個のスクラツバ―内で脱塵および脱硫し、この処理後の
排ガスを各送風機でひとつの煙道にまとめて1本の煙突
から大気中に放出している点に着目し、このような多数
個のスクラツバ―を用いる排ガスの処理方法において、
各スクラツバ―から排出される処理液を順次隣のスクラ
ツバ―側に移行させる処理流路をつくり、この処理流路
へのアルカリ試剤の投入方法を工夫することにより、各
スクラツバ―から導出する排ガス中のミストに起因した
排気経路での腐食の問題を軽減でき、かつアルカリ試剤
のロスの問題を回避できることを知り、本発明を完成す
るに至つた。
Means for Solving the Problems The present inventor has conducted extensive studies in order to achieve the above-mentioned object, and as a result, as described above, exhaust gas discharged from a large number of boilers in a power plant or the like is separated into separate scrubbing chambers. -Dust removal and desulfurization inside, and the exhaust gas after this treatment was collected into one flue by each blower and discharged from one chimney into the atmosphere. In the method of treating exhaust gas using
In the exhaust gas discharged from each scrubber, by creating a processing flow path that sequentially transfers the processing liquid discharged from each scrubber to the adjacent scrubber side and devising the method of adding the alkaline reagent to this processing flow path. The inventors have found that the problem of corrosion in the exhaust path due to the mist can be reduced and the problem of loss of the alkaline reagent can be avoided, and have completed the present invention.

【0012】すなわち、本発明は、並列する多数個のス
クラツバ―に灰分および硫黄酸化物を含む排ガスを導入
し、これに水およびアルカリ試剤からなる脱硫剤を含む
処理液を接触させて、排ガスの脱塵および脱硫を行い、
ついで、各スクラツバ―から導出する排ガスを各送風機
により煙突に導いて大気中に放出するにあたり、各スク
ラツバ―の処理液を順次隣のスクラツバ―側に移行させ
る処理流路を形成し、この処理流路における最初のスク
ラツバ―側に、各スクラツバ―に必要な脱硫剤の全量を
供給して、最終のスクラツバ―側の処理液のPHが約6
前後となるようにすることを特徴とする排ガスの処理方
法に係るものである。
That is, according to the present invention, an exhaust gas containing ash and sulfur oxides is introduced into a large number of parallel scrubbers, and a treatment liquid containing a desulfurizing agent consisting of water and an alkaline reagent is brought into contact with the scrubber to remove the exhaust gas. Dedust and desulfurize,
Next, when the exhaust gas discharged from each scrubber is guided to the chimney by each blower and discharged into the atmosphere, a processing flow path is formed to sequentially transfer the processing liquid of each scrubber to the adjacent scrubber side. The total amount of desulfurizing agent required for each scrubber is supplied to the first scrubber side in the route, and the pH of the treatment liquid on the final scrubber side is about 6
The present invention relates to a method for treating exhaust gas, which is characterized in that it is arranged before and after.

【0013】[0013]

【作用】本発明では、各スクラツバ―を結ぶ処理流路に
おける最初のスクラツバ―側に、各スクラツバ―に必要
な脱硫剤の全量を供給するため、最終のスクラツバ―側
に至る手前までは、処理液のPHは過剰のアルカリ試剤
によつて約7以上の高い値に保たれ、対応する各スクラ
ツバ―から導出する排ガスのミストは、そのドレンが酸
性化せず、直結する各送風機などを腐食する心配がな
い。
In the present invention, since the entire amount of the desulfurizing agent necessary for each scrubber is supplied to the first scrubber side in the processing flow path connecting the scrubbers, the treatment is performed before reaching the final scrubber side. The pH of the liquid is kept at a high value of about 7 or more due to the excess alkaline reagent, and the mist of the exhaust gas discharged from the corresponding scrubber does not acidify the drain and corrodes the blowers directly connected. Don't worry.

【0014】一方、上記の如く高いPHに設定すると、
各スクラツバ―から排出される処理液中にCO2 との反
応でMg(HCO3 2 などの塩が多量に含まれてくる
が、このものは最終のスクラツバ―側に至つたとき、処
理液のPHが6前後に設定されているため、脱硫反応に
分解利用され、重炭酸塩として系外に排出されることが
少なく、アルカリ試剤のロスが極力抑えられる。
On the other hand, when the high PH is set as described above,
Each Sukuratsuba - salts such as Mg (HCO 3) 2 by reaction with CO 2 comes contains a large amount in the processing solution discharged from, but this compound final Sukuratsuba - when there was Itaritsu the side, the processing solution Since the pH is set to around 6, it is used for decomposition in the desulfurization reaction and is rarely discharged as a bicarbonate to the outside of the system, and the loss of the alkaline reagent is suppressed as much as possible.

【0015】また、最終のスクラツバ―側をPH6前後
に設定すると、このスクラツバ―から導出する排ガスの
ミストに高濃度のMg(HSO3 2 などが含まれ、こ
れがドレンの酸性化の要因となつて、対応する送風機や
ダクトなどが腐食してくるおそれがある。このため、こ
れら送風機やダクトなどは、高価な耐酸性材質とした
り、高価な耐酸性ライニングを施す必要があるが、これ
による高コスト化は、全スクラツバ―の各送風機や各ダ
クトなどのうちのごく一部であるため、全体的にみる
と、大きなコストアツプとはならない。
Further, when the final scrubber side is set to around PH6, the exhaust gas mist derived from this scrubber contains a high concentration of Mg (HSO 3 ) 2 and the like, which is a cause of acidification of the drain. As a result, the corresponding blower or duct may be corroded. For this reason, these blowers and ducts need to be made of expensive acid-resistant material or have an expensive acid-resistant lining, but the cost increase due to this is that of all blowers and ducts of all scrubbers. As it is a small part, it is not a big cost up as a whole.

【0016】[0016]

【実施例】以下、本発明の実施例を図面にしたがつて説
明する。図1は、本発明の排ガスの処理方法を適用した
装置の概略構成図である。
Embodiments of the present invention will now be described with reference to the drawings. FIG. 1 is a schematic configuration diagram of an apparatus to which the exhaust gas treating method of the present invention is applied.

【0017】図1において、1(1A〜1E)は、並列
する5個のスクラツバ―で、ボイラ―2(2B〜2E)
から排ガスを導入し、これに、注水管3(3A〜3E)
および脱硫剤の貯槽4より、水およびMg(OH)2
水スラリ―を加えて、両者を接触させることにより、排
ガスの脱塵および脱硫を行うものである。
In FIG. 1, reference numeral 1 (1A to 1E) denotes five parallel scrubbers, which are boilers 2 (2B to 2E).
Exhaust gas is introduced from the water injection pipe 3 (3A to 3E)
Also, by adding water and water slurry of Mg (OH) 2 from the desulfurizing agent storage tank 4 and bringing them into contact with each other, the exhaust gas is dedusted and desulfurized.

【0018】5(5A〜5E)は、スクラツバ―1(1
A〜1E)から導出する排ガスを、煙道6にまとめて1
本の煙突7から大気中に放出する送風機である。8(8
A〜8E)は、その途中に上記の送風機5(5A〜5
E)を有するダクトであつて、上記の煙道6に接続され
ている。
5 (5A to 5E) is a scrubber 1 (1
The exhaust gas derived from A to 1E) is collected in the flue 6 and
This is a blower that is emitted from the chimney 7 of the book into the atmosphere. 8 (8
A-8E), the blower 5 (5A-5
A duct with E), which is connected to the flue 6 described above.

【0019】9は、各スクラツバ―1A〜1Eの処理液
を、順次、配管10(10A〜10E)により隣のスク
ラツバ―側に移行させる処理流路であつて、この処理流
路9の最初のスクラツバ―1A側に、各スクラツバ―1
A〜1Eに必要な脱硫剤の全量を、脱硫剤の貯槽4から
配管Lを介して供給するようになつており、その供給量
は、最終のスクラツバ―1E側の処理液のPHが約6前
後、つまり約5.7〜6.3程度となるように、自動制
御により調整されている。
Reference numeral 9 denotes a processing flow path for sequentially transferring the processing liquid of each of the scrubbers 1A to 1E to the adjacent scrubber side by a pipe 10 (10A to 10E). Each scrubber 1 on the side of the scrubber 1A
All the desulfurizing agents required for A to 1E are supplied from the desulfurizing agent storage tank 4 through the pipe L. The supply amount of the desulfurizing agent is about 6 when the pH of the treatment liquid on the final scrubber 1E side is about 6 It is adjusted by automatic control so that the front and rear, that is, about 5.7 to 6.3.

【0020】上記のスクラツバ―1(1A〜1E)は、
この例では、ベンチユリ―スクラツバ―にて構成されて
いる。図2に、スクラツバ―1Aの構成を示す。他のス
クラツバ―1B〜1Eもこれと全く同じである。図2
中、11はベンチユリ―管、12は塔型のサイクロン、
13は接続配管、14は処理液の受け槽、15は分級機
(液体サイクロン)、16はポンプである。
The above-mentioned scrubber-1 (1A-1E) is
In this example, it is composed of a bench-yuri scrubber. FIG. 2 shows the configuration of the scrubber 1A. The other scrubbers 1B-1E are exactly the same. Figure 2
Inside, 11 is a bench lily tube, 12 is a tower type cyclone,
Reference numeral 13 is a connection pipe, 14 is a processing liquid receiving tank, 15 is a classifier (hydrocyclone), and 16 is a pump.

【0021】この種のスクラツバ―は、排ガスGをベン
チユリ―管11の開口端側から導入して、その絞り部で
高速気流とし、注水管3(3A)より供給される水を細
滴に分散し、この水滴に排ガス中の灰分からなる塵埃粒
子を衝突付着させ、この付着水滴をガス流により接続配
管13を経てサイクロン12の塔下部に接線方向に導入
し、遠心力で塔壁に捕捉させて、塔底部に落下させる。
また別に、接続配管13において、脱硫剤であるMg
(OH)2 を含む処理液を供給し、排ガス中の硫黄酸化
物との反応を行わせて、脱硫生成物を得、上記の捕捉塵
埃とともに、サイクロンの塔底部に落下させる。
In this type of scrubber, the exhaust gas G is introduced from the open end side of the bench-free pipe 11 and is made into a high-speed air flow at its narrowed portion to disperse the water supplied from the water injection pipe 3 (3A) into fine droplets. Then, dust particles made of ash in the exhaust gas are made to collide with and adhere to the water droplets, and the adhered water droplets are introduced tangentially to the lower portion of the cyclone 12 through the connecting pipe 13 by the gas flow, and are caught by the tower wall by centrifugal force. Drop it to the bottom of the tower.
Separately, in the connection pipe 13, Mg which is a desulfurizing agent is used.
A treatment liquid containing (OH) 2 is supplied to cause a reaction with sulfur oxides in the exhaust gas to obtain a desulfurized product, and the desulfurized product is dropped to the bottom of the cyclone together with the captured dust.

【0022】このように灰分を捕捉しかつ脱硫生成物を
含んだ処理液は、塔底部から受け槽14に移され、ここ
で必要によりスパ―ジヤ―17から送り込まれる空気に
よつて酸化処理されたのち、ホンプ16により分級機
(液体サイクロン)15に供給され、ここで捕捉灰分を
取り除いた微細スラリ―は前記の接続配管13に循環供
給され、捕捉灰分を含む粗大スラリ―は配管10(10
A)により隣のスクラツバ―1(1B)(の受け槽)に
移行させる。なお、上記の分級機15は、液体サイクロ
ンに代えて、シツクナ―を用いてもよい。
The treatment liquid thus trapping the ash and containing the desulfurization product is transferred from the bottom of the tower to the receiving tank 14, where it is oxidized by the air sent from the sparger 17 if necessary. After that, it is supplied to a classifier (hydrocyclone) 15 by a horn 16, the fine slurry from which the captured ash is removed is circulated and supplied to the connection pipe 13, and the coarse slurry containing the captured ash is supplied to the pipe 10 (10).
By A), it is transferred to (the receiving tank for) the adjacent Scrubber-1 (1B). The classifier 15 described above may use a shockener instead of the liquid cyclone.

【0023】このような装置構成によると、各ボイラ―
2A〜2Eから排出される排ガスGは、対応する各スク
ラツバ―1A〜1Eに導入されて、上述の如く脱塵およ
び脱硫処理されるが、その際、各スクラツバ―1A〜1
Eに必要な脱硫剤の全量を、貯槽4からスクラツバ―1
A側にのみ供給し、かつこれが順次スクラツバ―1B→
1C→1D→1Eへと移行するため、スクラツバ―1D
までの処理液には、十分なアルカリ試剤、つまりMg
(OH)2 が存在することになる。
According to such an apparatus configuration, each boiler is
Exhaust gas G discharged from 2A to 2E is introduced into the corresponding scrubbers 1A to 1E and subjected to dedusting and desulfurization treatment as described above. At that time, the scrubbers 1A to 1E are treated.
The total amount of desulfurizing agent required for E is supplied from the storage tank 4 to the scrubber 1
It is supplied only to the A side, and this is the scrubber 1B →
Because of the shift from 1C → 1D → 1E, SCRATSUBA 1D
Sufficient alkali reagent, namely Mg
There will be (OH) 2 .

【0024】このため、スクラツバ―1A〜1Dの処理
液のPHは、いずれも約7以上の高い値に保たれるか
ら、これらスクラツバ―1A〜1Dより脱塵および脱硫
処理されて導出する排ガスG´は、ミスト中にMgSO
3 を多く含むことになり、そのドレンが酸性化すること
はない。したがつて、この排ガスG´を運ぶ送風機5A
〜5Dおよびダクト8A〜8Dは、腐食の心配がとくに
なく、安価なステンレス製材質としたり、通常のライニ
ングを施すだけでよい。
For this reason, since the PH of the treatment liquids of the scrubbers 1A to 1D is maintained at a high value of about 7 or more, the exhaust gas G discharged from the scrubbers 1A to 1D after being subjected to dedusting and desulfurization treatments. 'Is MgSO in the mist
It will contain a large amount of 3 , and the drain will not be acidified. Therefore, the blower 5A carrying this exhaust gas G '
.About.5D and ducts 8A to 8D have no particular concern about corrosion, and may be made of an inexpensive stainless steel material or may be provided with a normal lining.

【0025】また、上記の如く高いPHに設定すると、
スクラツバ―1A〜1Dから排出される処理液中にCO
2 との反応でMg(HCO3 2 などの塩が多量に含ま
れてくるが、このものは最終のスクラツバ―1E(の受
け槽14)側に至つたとき、処理液のPHが約6前後に
設定されているため、脱硫反応にうまく分解利用され、
重炭酸塩として系外に排出されることがない。
If the high PH is set as described above,
CO in the treatment liquid discharged from the scrubber 1A to 1D.
A large amount of salts such as Mg (HCO 3 ) 2 are included in the reaction with 2 , but when this reaches the final side of the scrubber 1E (reception tank 14), the pH of the treatment liquid is about 6 Since it is set before and after, it can be decomposed and utilized well for desulfurization reaction,
It is not discharged outside the system as bicarbonate.

【0026】したがつて、この最終のスクラツバ―1E
(の分級機15)側から配管10Eによつて系外に排出
される処理液は、各スクラツバ―1A〜1Eで捕捉した
すべての灰分を主固形分として含み、かつ液中に硫酸マ
グネシウムなどの脱硫生成物を含む水スラリ―であり、
アルカリ試剤のロスが極力抑えられた状態で系外に排出
されて、適宜廃棄または回収処理される。
Therefore, this final Scratuba-1E
The treatment liquid discharged from the (classifier 15) side to the outside of the system through the pipe 10E contains all the ash content captured by each of the scrubbers 1A to 1E as the main solid content, and contains magnesium sulfate or the like in the liquid. A water slurry containing desulfurization products,
It is discharged to the outside of the system with the loss of the alkaline reagent being suppressed as much as possible, and appropriately disposed or collected.

【0027】一方、最終のスクラツバ―1Eより脱塵お
よび脱硫処理されて導出する排ガスG´は、処理液のP
Hが約6前後に設定されているため、ミストに高濃度の
Mg(HSO3 2 などが含まれ、これがドレンの酸性
化の要因となるので、この排ガスG´を運ぶ送風機5E
およびダクト8Eは、腐食の心配がある。したがつて、
これらについては、高価な耐酸性材質としたり、高価な
耐酸性ライニングを施すなどの対策が必要となるが、既
述のように、他の送風機5A〜5Dやダクト8A〜8D
は安価な材質などにて対応できるため、全体的には、大
きなコストアツプとはならず、経済的な設備費にてまか
なえる。
On the other hand, the exhaust gas G'which is dedusted and desulfurized from the final scrubber 1E and is discharged is P of the treatment liquid.
Since H is set at around 6, high-concentration Mg (HSO 3 ) 2 etc. is contained in the mist, which causes acidification of the drain, so the blower 5E carrying this exhaust gas G '
And the duct 8E may be corroded. Therefore,
For these, it is necessary to take measures such as using an expensive acid resistant material or applying an expensive acid resistant lining, but as already mentioned, other blowers 5A to 5D and ducts 8A to 8D are used.
Since it is possible to use low cost materials etc., the overall cost does not increase, and economical equipment cost can be covered.

【0028】しかも、この実施例に示すように、ダクト
8A〜8Eから導かれる排ガスG´をすべて煙道6にま
とめて1本の煙突7より大気中に放出する場合は、ダク
ト8A側が煙突7に最も近い位置、換言すればダクト8
E側が煙突7より最も遠ざかる位置となるようにすれ
ば、ダクト8Eから排出される酸性ミストを含む排ガス
G´が、ダクト8D〜8Aから排出されるアルカリ性ミ
ストを含む排ガスG´によつて、希釈されることにな
る。
Moreover, as shown in this embodiment, when all the exhaust gases G'guided from the ducts 8A to 8E are collected in the flue 6 and discharged into the atmosphere from one chimney 7, the duct 8A side is the chimney 7. Position closest to, in other words duct 8
If the E side is located farthest from the chimney 7, the exhaust gas G ′ containing the acidic mist discharged from the duct 8E is diluted by the exhaust gas G ′ containing the alkaline mist discharged from the ducts 8D to 8A. Will be done.

【0029】このため、煙道6のダクト8E側は耐酸性
ライニングが求められても、それ以降のダクト8D〜8
Aではそれほど高価なライニングを必要とせず、とくに
煙突7ではほとんど酸性ミストの影響を受けなくなるた
め、通常のライニングで十分に対応でき、この点も、経
済的に大きな利点となる。
Therefore, even if the acid-resistant lining is required on the duct 8E side of the flue 6, the ducts 8D to 8D thereafter are provided.
A does not require a very expensive lining, and the chimney 7 is almost unaffected by the acid mist. Therefore, a normal lining is sufficient, and this is also a great economical advantage.

【0030】なお、上記の実施例では、ボイラ―2A〜
2Eから排出される排ガスを各スクラツバ―1A〜1E
に導入した例を示しているが、たとえば、ボイラ―2A
の排ガス量が非常に多い場合、これを分割して、各スク
ラツバ―1A〜1Eに導入するようにしてもよい。ま
た、スクラツバ―1は、上記のベンチユリ―スクラツバ
―に限らず、多孔板型のスクラツバ―など、湿式法とし
て知られる各種のスクラツバ―を使用でき、その個数も
上記の5個に限定されず、2個以上、好ましくは3個以
上の任意の個数を選択できる。
In the above embodiment, the boiler-2A-
Exhaust gas discharged from 2E is used for each scrubber 1A to 1E.
Introduced in the example, the boiler-2A
When the amount of exhaust gas is extremely large, it may be divided and introduced into each of the scrubbers 1A to 1E. Further, the scrubber 1 is not limited to the above bench Yury scrubber, and various scrubbers known as a wet method such as a perforated plate type scrubber can be used, and the number thereof is not limited to the above five, Any number of 2 or more, preferably 3 or more can be selected.

【0031】また、脱硫剤として用いるアルカリ試剤
は、上記のMg(OH)2 のほかに、CaO、Ca(O
H)2 などのMgやCaを含む各種の化合物を使用で
き、苛性ソ―ダや苛性カリなどを用いてもよい。いずれ
のアルカリ試剤を用いても、上記と同様の作用効果が奏
される。
Alkaline agents used as desulfurizing agents include CaO and Ca (O) in addition to the above Mg (OH) 2.
Various compounds containing Mg and Ca such as H) 2 can be used, and caustic soda and caustic potash may be used. Regardless of which alkaline reagent is used, the same action and effect as described above can be obtained.

【0032】[0032]

【発明の効果】以上のように、本発明によれば、排気経
路における送風機などの腐食の問題を軽減できるととも
に、アルカリ試剤のロスの問題を回避でき、経済的に有
利な排ガスの処理方法を提供することができる。
As described above, according to the present invention, it is possible to reduce the problem of corrosion of the blower and the like in the exhaust path, avoid the problem of alkali reagent loss, and provide an economically advantageous exhaust gas treatment method. Can be provided.

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

【図1】本発明の排ガスの処理方法を適用した装置の概
略構成図である。
FIG. 1 is a schematic configuration diagram of an apparatus to which an exhaust gas treating method of the present invention is applied.

【図2】本発明の排ガスの処理方法に用いたスクラツバ
―の概略構成図である。
FIG. 2 is a schematic configuration diagram of a scrubber used in the exhaust gas treatment method of the present invention.

【符号の説明】[Explanation of symbols]

1(1A〜1E) スクラツバ― 3(3A〜3E) 注水管 4 Mg(OH)2 の水スラリ―からなる脱硫剤の貯槽 5(5A〜5E) 送風機 7 煙突 9 処理流路 10(10A〜10E) 処理液を隣のスクラツバ―側
に移行させる配管 G 処理前の排ガス G´ 処理後の排ガス
1 (1A to 1E) Scrubber 3 (3A to 3E) Water injection pipe 4 Storage tank of desulfurizing agent consisting of Mg (OH) 2 water slurry 5 (5A to 5E) Blower 7 Chimney 9 Processing flow path 10 (10A to 10E) ) Piping for transferring the treatment liquid to the adjacent scrubber side G Exhaust gas before treatment G ′ Exhaust gas after treatment

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 並列する多数個のスクラツバ―に灰分お
よび硫黄酸化物を含む排ガスを導入し、これに水および
アルカリ試剤からなる脱硫剤を含む処理液を接触させ
て、排ガスの脱塵および脱硫を行い、ついで、各スクラ
ツバ―から導出する排ガスを各送風機により煙突に導い
て大気中に放出するにあたり、各スクラツバ―の処理液
を順次隣のスクラツバ―側に移行させる処理流路を形成
し、この処理流路における最初のスクラツバ―側に、各
スクラツバ―に必要な脱硫剤の全量を供給して、最終の
スクラツバ―側の処理液のPHが約6前後となるように
することを特徴とする排ガスの処理方法。
1. Dedusting and desulfurization of exhaust gas by introducing exhaust gas containing ash and sulfur oxides into a large number of parallel scrubbers and contacting this with a treatment liquid containing a desulfurizing agent consisting of water and an alkaline reagent. Then, in guiding the exhaust gas discharged from each scrubber to the chimney by each blower and releasing it into the atmosphere, a processing flow path for sequentially transferring the processing liquid of each scrubber to the adjacent scrubber side is formed, The first scrubber side in this treatment channel is supplied with the total amount of desulfurizing agent required for each scrubber so that the pH of the treatment liquid on the final scrubber side is about 6 or less. Exhaust gas treatment method.
JP4350654A 1992-12-04 1992-12-04 Treatment of exhaust gas Pending JPH06170153A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4350654A JPH06170153A (en) 1992-12-04 1992-12-04 Treatment of exhaust gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4350654A JPH06170153A (en) 1992-12-04 1992-12-04 Treatment of exhaust gas

Publications (1)

Publication Number Publication Date
JPH06170153A true JPH06170153A (en) 1994-06-21

Family

ID=18411954

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4350654A Pending JPH06170153A (en) 1992-12-04 1992-12-04 Treatment of exhaust gas

Country Status (1)

Country Link
JP (1) JPH06170153A (en)

Cited By (10)

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Publication number Priority date Publication date Assignee Title
WO2003066198A1 (en) * 2000-08-10 2003-08-14 Mineral Fine-Chemicals,Inc. Additive for exhaust gas, method of manufacturing the additive, and method for power generation using the additive
JP2014140786A (en) * 2013-01-22 2014-08-07 Shin Etsu Chem Co Ltd Waste gas treatment system and waste gas treatment method of chlorosilane
JP2018502711A (en) * 2015-01-09 2018-02-01 エクソンモービル アップストリーム リサーチ カンパニー Separation of impurities from fluid streams using dual cocurrent contactors.
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Publication number Priority date Publication date Assignee Title
WO2003066198A1 (en) * 2000-08-10 2003-08-14 Mineral Fine-Chemicals,Inc. Additive for exhaust gas, method of manufacturing the additive, and method for power generation using the additive
JP2014140786A (en) * 2013-01-22 2014-08-07 Shin Etsu Chem Co Ltd Waste gas treatment system and waste gas treatment method of chlorosilane
US10343107B2 (en) 2013-05-09 2019-07-09 Exxonmobil Upstream Research Company Separating carbon dioxide and hydrogen sulfide from a natural gas stream using co-current contacting systems
JP2018502711A (en) * 2015-01-09 2018-02-01 エクソンモービル アップストリーム リサーチ カンパニー Separation of impurities from fluid streams using dual cocurrent contactors.
US10300429B2 (en) 2015-01-09 2019-05-28 Exxonmobil Upstream Research Company Separating impurities from a fluid stream using multiple co-current contactors
US10717039B2 (en) 2015-02-17 2020-07-21 Exxonmobil Upstream Research Company Inner surface features for co-current contractors
US10391442B2 (en) 2015-03-13 2019-08-27 Exxonmobil Upstream Research Company Coalescer for co-current contractors
US10486100B1 (en) 2015-03-13 2019-11-26 Exxonmobil Upstream Research Company Coalescer for co-current contactors
US11000795B2 (en) 2017-06-15 2021-05-11 Exxonmobil Upstream Research Company Fractionation system using compact co-current contacting systems
US11260342B2 (en) 2017-06-15 2022-03-01 Exxonmobil Upstream Research Company Fractionation system using bundled compact co-current contacting systems
US10876052B2 (en) 2017-06-20 2020-12-29 Exxonmobil Upstream Research Company Compact contacting systems and methods for scavenging sulfur-containing compounds
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