JP2994913B2 - Wet flue gas desulfurization apparatus using magnesium oxide and desulfurization method thereof - Google Patents

Wet flue gas desulfurization apparatus using magnesium oxide and desulfurization method thereof

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Publication number
JP2994913B2
JP2994913B2 JP5171457A JP17145793A JP2994913B2 JP 2994913 B2 JP2994913 B2 JP 2994913B2 JP 5171457 A JP5171457 A JP 5171457A JP 17145793 A JP17145793 A JP 17145793A JP 2994913 B2 JP2994913 B2 JP 2994913B2
Authority
JP
Japan
Prior art keywords
magnesium oxide
flue gas
wet
gas
absorption 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.)
Expired - Fee Related
Application number
JP5171457A
Other languages
Japanese (ja)
Other versions
JPH0724252A (en
Inventor
一隆 富松
新一 滝本
吉博 北
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP5171457A priority Critical patent/JP2994913B2/en
Priority to TW083106138A priority patent/TW306885B/zh
Priority to ITRM940444A priority patent/IT1272321B/en
Priority to CN94108254A priority patent/CN1048188C/en
Priority to KR1019940016701A priority patent/KR0125122B1/en
Publication of JPH0724252A publication Critical patent/JPH0724252A/en
Application granted granted Critical
Publication of JP2994913B2 publication Critical patent/JP2994913B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1456Removing acid components
    • B01D53/1481Removing sulfur dioxide or sulfur trioxide
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D47/00Separating dispersed particles from gases, air or vapours by liquid as separating agent
    • B01D47/02Separating dispersed particles from gases, air or vapours by liquid as separating agent by passing the gas or air or vapour over or through a liquid bath
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1493Selection of liquid materials for use as absorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/346Controlling the process
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/48Sulfur compounds
    • B01D53/50Sulfur oxides
    • B01D53/501Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound
    • B01D53/502Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound characterised by a specific solution or suspension
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/77Liquid phase processes
    • B01D53/78Liquid phase processes with gas-liquid contact
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/81Solid phase processes
    • B01D53/83Solid phase processes with moving reactants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/40Alkaline earth metal or magnesium compounds
    • B01D2251/402Alkaline earth metal or magnesium compounds of magnesium

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は煙道ガス中のSOx を除
去する湿式排煙脱硫装置に関する。
The present invention relates to a wet type exhaust gas desulfurization apparatus for removing SO x in the flue gases.

【0002】[0002]

【従来の技術】従来、マグネシウムを利用した排煙脱硫
装置としては吸収剤として水酸化マグネシウムを用いる
方法が公知である。図2にそのフローを示すが、煙道ガ
スは冷却ライン20により水露点近く迄増湿冷却された
後、吸収塔9へ導かれ、吸収液循環ライン7より供給さ
れる吸収液のスプレイと充てん層8により、効率良く気
液反応によりSOx を吸収される。
2. Description of the Related Art Conventionally, as a flue gas desulfurization apparatus using magnesium, a method using magnesium hydroxide as an absorbent is known. FIG. 2 shows the flow. The flue gas is humidified and cooled by the cooling line 20 to near the water dew point, then guided to the absorption tower 9 and sprayed and filled with the absorbent supplied from the absorbent circulation line 7. The layer 8 efficiently absorbs SO x by a gas-liquid reaction.

【0003】また、排ガス中にSO3 を含む場合、従来
の湿式の脱硫装置では冷却過程でSO3 が微細ミスト化
してしまうためにSO3 は液とミストの接触でしか除去
されないため、その除去効率が低く、このため排煙脱硫
装置からのSO3 のミストが除去されずに排出されてし
まうといった問題があり、そのため、SO3 を除去する
湿式電気集塵機23を排脱装置の出口に設置している例
もある。
[0003] Also, since if in the exhaust gas containing SO 3, which SO 3 because the SO 3 in the cooling process results in a fine mist in the desulfurization apparatus of the conventional wet are not only removed at the contact of the liquid and mist, the removal There is a problem that the efficiency is low, and the mist of SO 3 from the flue gas desulfurization device is discharged without being removed. Therefore, the wet electric dust collector 23 for removing SO 3 is installed at the outlet of the removal device. There are also examples.

【0004】なお、図2において21は水酸化マグネシ
ウム供給槽で、この槽21内から水マグ供給ポンプ22
によって水酸化マグネシウムが吸収塔9内へ供給され
る。10は循環液スプレライン7及び冷却ライン20へ
循環液を送るポンプである。11は排水処理ユニット、
24は煙突を示している。13は酸化ブロワである。
[0004] In FIG. 2, reference numeral 21 denotes a magnesium hydroxide supply tank.
Thus, magnesium hydroxide is supplied into the absorption tower 9. Reference numeral 10 denotes a pump for sending the circulating liquid to the circulating liquid spray line 7 and the cooling line 20. 11 is a wastewater treatment unit,
24 indicates a chimney. 13 is an oxidation blower.

【0005】また、酸化マグネシウムを吸収剤として用
いる例もあるが、その場合には酸化マグネシウムを水酸
化マグネシウムに変換し吸収剤として使用している。従
って、酸化マグネシウムを吸収剤として用いる場合、従
来の例では酸化マグネシウムを水酸化マグネシウムに水
和するための設備が必要であり、水酸化マグネシウムを
吸収剤として用いるよりもランニングコストは低減出来
るものの、水和のための設備費が必要であった。
In some cases, magnesium oxide is used as an absorbent. In that case, magnesium oxide is converted to magnesium hydroxide and used as an absorbent. Therefore, when using magnesium oxide as an absorbent, in the conventional example, equipment for hydrating magnesium oxide to magnesium hydroxide is required, and although running costs can be reduced as compared with using magnesium hydroxide as an absorbent, Equipment costs for hydration were required.

【0006】[0006]

【発明が解決しようとする課題】本発明は、酸化マグネ
シウムを吸収剤として、排ガス中に含まれるSO3 を効
率良く除去すると共に、酸化マグネシウムを水和するた
めの設備を必要としない湿式排煙脱硫装置を提供するこ
とを課題としている。また、本発明は酸化マグネシウム
の反応活性を高めることのできる吸収塔をもつ湿式排煙
脱硫装置を提供することをも課題としている。
DISCLOSURE OF THE INVENTION The present invention is directed to a wet flue gas system which uses magnesium oxide as an absorbent to efficiently remove SO 3 contained in exhaust gas and does not require equipment for hydrating magnesium oxide. It is an object to provide a desulfurization device. Another object of the present invention is to provide a wet flue gas desulfurization apparatus having an absorption tower capable of increasing the reaction activity of magnesium oxide.

【0007】更にまた、本発明はスケーリング等の問題
を生ずることなしに前記した装置により安定したSOx
除去効率を維持できる湿式排煙脱硫方法を提供すること
を課題としている。
Furthermore, the present invention provides a more stable SO x by the above-described apparatus without causing problems such as scaling.
It is an object of the present invention to provide a wet flue gas desulfurization method capable of maintaining the removal efficiency.

【0008】[0008]

【課題を解決するための手段】本発明は、SO2 とSO
3 の両方を含む重油焚ボイラ等の排ガス処理において、
SO3 ガスを除去するための手段として、酸化マグネシ
ウム(MgO)の粉体を煙道に直接噴霧し、その粉体は
後段の湿式の吸収塔の循環液で捕集し、スラリの状態で
SOx ガスの吸収剤として利用する。また粉体のMgO
をSOx の湿式吸収に効率良く利用するためにMgOを
水酸化マグネシウム(Mg(OH)2) 迄水和せず、亜硫
酸イオンを含む循環液で直接捕集させる。その結果、M
gOの溶解性が高まり吸収剤としての活性が高まる。
According to the present invention, SO 2 and SO 2 are provided.
In exhaust gas treatment of heavy oil-fired boilers including both
As a means for removing SO 3 gas, powder of magnesium oxide (MgO) is directly sprayed on a flue, and the powder is collected by a circulating liquid of a later-stage wet-type absorption tower, and the SO 3 is collected in a slurry state. Used as x gas absorber. The powder MgO
In order to efficiently utilize the compound for wet absorption of SO x , MgO is not hydrated to magnesium hydroxide (Mg (OH) 2 ), but is directly collected by a circulating liquid containing sulfite ions. As a result, M
The solubility of gO increases, and the activity as an absorbent increases.

【0009】また、他の本発明による湿式排煙脱硫装置
では、前記した手段に加え、前記循環液中に一定量の亜
硫酸イオンを確保するため吸収塔内に酸化抑制手段を有
する構成を採用する。この酸化抑制手段は循環液中の亜
硫酸イオンが少なくなると吸収塔底に送られる酸化空気
量を抑制する装置とすることができる。
Further, in another wet flue gas desulfurization apparatus according to the present invention, in addition to the above-mentioned means, a constitution having an oxidation suppressing means in the absorption tower is employed in order to secure a fixed amount of sulfite ions in the circulating liquid. . This oxidation suppressing means can be a device for suppressing the amount of oxidized air sent to the bottom of the absorption tower when the amount of sulfite ions in the circulating liquid decreases.

【0010】更にまた本発明においては、前記した湿式
排煙脱硫装置において、排ガス中のSO2 濃度とガス流
量並びに吸収塔内の液中のPH値を基に酸化マグネシウ
ムの注入量を制御する湿式排煙脱硫方法を採用する。
Further, according to the present invention, in the above-mentioned wet flue gas desulfurization apparatus, the wet-type flue gas desulfurization apparatus controls the injection amount of magnesium oxide based on the SO 2 concentration and the gas flow rate in the exhaust gas and the PH value in the liquid in the absorption tower. Adopt flue gas desulfurization method.

【0011】[0011]

【作用】酸化マグネシウムは炭酸マグネシウムをか焼し
たものが比較的安いコストで市販されており、また粒径
も10〜数10μmの微細な粉体が市販されている。こ
の粉体をSOx を含むボイラ排ガス中に噴霧させること
により、ガス中のSO3と反応させることが可能であ
る。ここに粉体の噴霧する場所はボイラであればエアヒ
ータの出口煙道であり、150〜200℃の酸露点以上
の温度領域が望ましく、固気反応時間を確保するために
は湿式吸収塔よりも離れた出来る限り上流側が望まし
い。
The magnesium oxide obtained by calcining magnesium carbonate is commercially available at a relatively low cost, and the fine powder having a particle size of 10 to several tens μm is commercially available. By spraying this powder into a boiler exhaust gas containing SO x , it is possible to react with SO 3 in the gas. Here, the place where the powder is sprayed is the exit flue of the air heater in the case of a boiler, and a temperature range of an acid dew point of 150 to 200 ° C. or higher is desirable. It is desirable to be as far upstream as possible.

【0012】一般に煙道ガス中の速度は15m/s以上
の流速があり、市販の酸化マグネシウムはガス中を沈降
することなく後流の湿式吸収塔へ導かれる。一方、酸化
マグネシウムの投入量は、SO2 と当量近くに設定する
ことにより対SO3 に対しては十分な当量比を確保する
ことが可能である。(MgOとSO2 のモル比を1とす
れば,SO3 はSO2 の約1〜2%程度のため、SO3
に対してのモル比は50近くになる。)従ってSO3
MgOは固気反応ではあるが、SO3 に対するMgO比
を高くすることにより、十分なSO3 の除去効率が期待
出来る。SO3 はMgOと反応しMgSO4 (硫酸マグ
ネシウム)となる。
Generally, the velocity in the flue gas is 15 m / s or more, and commercially available magnesium oxide is guided to the downstream wet absorption tower without sedimentation in the gas. On the other hand, by setting the input amount of magnesium oxide close to the equivalent of SO 2 , it is possible to secure a sufficient equivalent ratio to SO 3 . (Assuming that the molar ratio of MgO and SO 2 is 1, SO 3 is about 1 to 2% of SO 2 , so SO 3
Is close to 50. ) Thus although SO 3 and MgO is in solid-gas reactions, by increasing the MgO ratio SO 3, sufficient SO 3 removal efficiency can be expected. SO 3 reacts with MgO to form MgSO 4 (magnesium sulfate).

【0013】次に未反応のMgOの粉体と一部硫酸マグ
ネシウムとなった粉体は湿式の吸収塔へ導かれ、循環液
と接触することにより、液中にとり込まれ、うすいスラ
リーを形成する。ここで、MgSO4 は溶解性が高いた
め、液で溶解しスケーリングの問題は発生しない。湿式
の吸収塔以降については基本的には従来の水マグ法と同
様であるが、酸化マグネシウムの粉体による閉塞を防止
するため、吸収塔はダウンフローとし、かつ気液比を十
分にとることが望ましい。
Next, the unreacted MgO powder and the powder partially converted to magnesium sulfate are led to a wet absorption tower, and brought into contact with the circulating liquid to be taken into the liquid to form a thin slurry. . Here, since MgSO 4 has high solubility, it is dissolved in a liquid, and the scaling problem does not occur. After the wet absorption tower, it is basically the same as the conventional water mug method, except that the absorption tower must be downflowed and have a sufficient gas-liquid ratio to prevent clogging with magnesium oxide powder. Is desirable.

【0014】次に、本発明によって吸収塔内における酸
化制御手段を設けた構成の装置としたものでは、酸化マ
グネシウムの反応活性を上げるために循環液中の亜硫酸
イオンを一定量確保して運転することにより、酸化マグ
ネシウムの溶解が促進され、その結果SO2 の安定的吸
収が可能となる。
Next, in the apparatus according to the present invention provided with an oxidation control means in the absorption tower, a certain amount of sulfite ions in the circulating liquid is secured to increase the reaction activity of magnesium oxide. Thereby, dissolution of magnesium oxide is promoted, and as a result, stable absorption of SO 2 becomes possible.

【0015】また、本発明による装置において、吸収塔
の液中のPHを一定の範囲で管理しながら、ガス中のS
x とガス流量に応じた量の酸化マグネシウムを投入す
る脱硫方法を採用すれば、SO2 ,SO3 の変動に対し
てもスケーリング等の問題を生ずることなく安定した除
去効率を維持することが可能である。
Further, in the apparatus according to the present invention, while controlling the pH in the liquid in the absorption tower within a certain range, the S in the gas is controlled.
By adopting a desulfurization method in which an amount of magnesium oxide corresponding to O x and a gas flow rate is adopted, it is possible to maintain a stable removal efficiency without causing a problem such as scaling with respect to fluctuations of SO 2 and SO 3. It is possible.

【0016】[0016]

【実施例】以下、本発明による酸化マグネシウムを用い
た排煙脱硫装置を図1に示した一実施例に基づいて具体
的に説明する。なお、図1において図2と同じ部分には
同一符号を付してあり、それらについては重複する説明
を省略する。図1において、煙道にはSOx ( SO2
SO3 )を含むガスが流れており、その中にノズル6に
より10〜数10μmの酸化マグネシウムの粉末が供給
される。酸化マグネシウムの粉末は貯蔵ホッパ1より定
量的にフィーダ2より切出され、ジェットコンベア3等
の手段により加圧され、煙道ガス中へ供給される。4は
ブロアである。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, a flue gas desulfurization apparatus using magnesium oxide according to the present invention will be described in detail with reference to an embodiment shown in FIG. In FIG. 1, the same parts as those in FIG. 2 are denoted by the same reference numerals, and a duplicate description thereof will be omitted. In FIG. 1, a gas containing SO x (SO 2 and SO 3 ) flows through the flue, and a nozzle 6 supplies magnesium oxide powder of 10 to several tens μm into the flue. The magnesium oxide powder is quantitatively cut out from the feeder 2 from the storage hopper 1, pressurized by means such as a jet conveyor 3, and supplied to the flue gas. 4 is a blower.

【0017】酸化マグネシウムの噴霧は均一に煙道ガス
内に行なわれることが望ましいことは言うまでもない。
噴霧された酸化マグネシウムは煙道ガス中を浮遊しなが
らSO3 を吸収しつつ、直接湿式の吸収塔9へ導かれ
る。吸収塔9内に導かれた酸化マグネシウムは循環液の
スプレライン7によりスプレさわる多量の循環水により
接触捕集される。ここで酸化マグネシウムは粒径が10
μm以上あるため、容易に湿式のスプレ捕集可能であ
る。
It is needless to say that it is desirable to spray the magnesium oxide uniformly into the flue gas.
The sprayed magnesium oxide is directly guided to the wet absorption tower 9 while absorbing SO 3 while floating in the flue gas. The magnesium oxide guided into the absorption tower 9 is contacted and collected by a large amount of circulating water sprayed by the circulating liquid spray line 7. Here, magnesium oxide has a particle size of 10
Since it is at least μm, wet spray collection can be easily performed.

【0018】循環水は吸収塔9の中を落下しながらSO
2 と気液接触しつつ下方へと落下する。このときの気液
接触効率を高めるため、充てん層8の設置が有効である
が、充てん層8はデポジットの発生が生じない様な構
造、例えばグリッドなどが良いのはいうまでもない。循
環液は塔底より循環ポンプ10により再循環され使用さ
れるが、液中の塩濃度が上がりすぎない様に外部より水
を導入し、かつ一部を抜出し排水処理設備11へ移送す
る方法は従来の水マグ法排脱装置と同じである。
The circulating water falls in the absorption tower 9 while
Drops downward while in gas-liquid contact with 2 . In order to increase the gas-liquid contact efficiency at this time, it is effective to provide the packed layer 8. However, it is needless to say that the filled layer 8 has a structure in which no deposit occurs, for example, a grid. The circulating liquid is recycled from the bottom of the tower by the circulating pump 10 and used. The method of introducing water from the outside so that the salt concentration in the liquid does not rise excessively, extracting a part of the liquor, and transferring it to the wastewater treatment facility 11 is as follows. It is the same as the conventional water mug method discharge device.

【0019】また、循環液中に一定以上の亜硫酸イオン
を確保するために亜硫酸イオン濃度の検出装置18によ
り循環液中の亜硫酸イオンを検出し、亜硫酸イオンが少
なくなると酸化ブロワ13による塔底の酸化を抑制する
制御弁19により、酸化ノズル12からの酸化空気量を
抑制する。液中の亜硫酸イオンの存在により、MgOの
活性度は従来の水酸化マグネシウム(Mg(OH)2)の
スラリ並に向上させることが可能となる。
Further, in order to secure a certain amount or more of sulfite ions in the circulating fluid, the sulfite ions in the circulating fluid are detected by a sulfite ion concentration detecting device 18. The control valve 19 suppresses the amount of oxidizing air from the oxidizing nozzle 12. Due to the presence of sulfite ions in the liquid, the activity of MgO can be improved to the level of a conventional slurry of magnesium hydroxide (Mg (OH) 2 ).

【0020】なお、図1では酸化空気量を、自動制御し
ているが、予め負荷条件が明らかな運転をする例では手
動にて酸化空気量を調整することが可能である。
Although the amount of oxidizing air is automatically controlled in FIG. 1, it is possible to manually adjust the amount of oxidizing air in an example in which an operation in which the load condition is clear is performed in advance.

【0021】また、MgO粉体の供給量はガス中のSO
x 濃度検出器16とガス流量検出器17より与えられる
信号に基づき制御ユニット14にてSOx 負荷に応じた
量を供給するよう制御される。また塔内でのスケーリン
グ等の問題が発生しないようPH検出器15の信号が制
御ユニット14へ送られ一定の領域に入る様に供給量を
制御する。
The supply amount of the MgO powder is controlled by the amount of SO in the gas.
It is controlled to provide the amount corresponding to the SO x loading at x concentration detector 16 and a gas flow detector 17 on the basis of a signal supplied from the control unit 14. Further, the signal of the PH detector 15 is sent to the control unit 14 to control the supply amount so as to enter a certain area so that a problem such as scaling in the tower does not occur.

【0022】[0022]

【発明の効果】以上具体的に説明したように、本発明に
よる酸化マグネシウムを用いた湿式排煙脱硫装置におい
ては、ガス中のSOx 濃度に応じた酸化マグネシウムの
煙道内への粉体吹込みにより、SOx をガス状のまま除
去することが可能となる。また煙道内に飛散した酸化マ
グネシウムの粉体を従来の湿式吸収塔の構成にて循環水
のスプレで捕集することにより、吸収剤の補給と粉体の
回収の両方を行なうことが出来る。
As it has been specifically described according to the present invention, in the wet flue gas desulfurization apparatus using the magnesium oxide of the present invention, a powder blowing to flue magnesium oxide in accordance with the SO x concentration in the gas This makes it possible to remove SO x in a gaseous state. In addition, by collecting the magnesium oxide powder scattered in the flue with a circulating water spray in a conventional wet-type absorption tower configuration, both replenishment of the absorbent and recovery of the powder can be performed.

【0023】特に酸化抑制手段を設けることにより循環
液の亜硫酸イオンを一定量確保する構成を採用したもの
では、酸化マグネシウムの活性が増大するため、MgO
をMg(OH)2に水和するための特別な設備は不要とな
り、上記のSO3 の除去効果と併せ、マグネシウム法排
脱の機能向上と大幅な建設費のコストダウン、さらには
安価な酸化マグネシウム吸収剤の使用によるランニング
コストの低減が図れる。
In particular, in the case of adopting a structure in which a certain amount of sulfite ions in the circulating fluid is secured by providing an oxidation suppressing means, the activity of magnesium oxide is increased.
No special equipment for hydrating Mg to Mg (OH) 2 is required, and in addition to the above-mentioned SO 3 removal effect, the function of eliminating the magnesium method is improved, the construction cost is significantly reduced, and the inexpensive oxidation is also performed. The running cost can be reduced by using the magnesium absorbent.

【0024】また、本発明による運転方法を採用するこ
とによってスケーリング等の問題を生ずることなくSO
x 負荷に適合した本発明排煙脱硫装置の安定した運転が
行われる。
Further, by adopting the operation method according to the present invention, the SO method can be realized without causing a problem such as scaling.
x Stable operation of the flue gas desulfurization apparatus of the present invention suitable for the load is performed.

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

【図1】本発明の一実施例による湿式排煙脱硫装置の機
器構成を一部断面で示す配置図。
FIG. 1 is a layout view showing a partial cross section of a device configuration of a wet flue gas desulfurization apparatus according to an embodiment of the present invention.

【図2】従来の水マグ法排煙脱硫装置の機器構成を一部
断面で示す配置図。
FIG. 2 is a layout diagram showing a partial cross-sectional view of a device configuration of a conventional water mug method flue gas desulfurization apparatus.

【符号の説明】[Explanation of symbols]

1 酸化マグネシウム貯蔵ホッパ 2 定量フィーダ 3 ジェットコンベア 4 ブロワ 5 煙道 6 吹込ノズル 7 循環液スプレライン 8 充てん層 9 吸収塔 10 ポンプ 11 排水処理ユニット 12 酸化ノズル 13 酸化ブロワ 14 制御ユニット 15 PH計 16 SOx 計 17 流量計 18 亜硫酸濃度計 19 制御弁 20 冷却ライン 21 水酸化マグネシウム供給槽 22 水マグ供給ポンプ 23 湿式電気集塵機 24 煙突DESCRIPTION OF SYMBOLS 1 Magnesium oxide storage hopper 2 Quantitative feeder 3 Jet conveyor 4 Blower 5 Flue 6 Blow nozzle 7 Circulating fluid spray line 8 Packing layer 9 Absorption tower 10 Pump 11 Wastewater treatment unit 12 Oxidation nozzle 13 Oxidation blower 14 Control unit 15 PH meter 16 SO x Total 17 Flow meter 18 Sulfurous acid concentration meter 19 Control valve 20 Cooling line 21 Magnesium hydroxide supply tank 22 Water mag supply pump 23 Wet electric dust collector 24 Chimney

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭61−167431(JP,A) 特開 平6−304442(JP,A) (58)調査した分野(Int.Cl.6,DB名) B01D 53/50 B01D 53/34 B01D 53/77 B01D 53/81 ────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-61-167431 (JP, A) JP-A-6-304442 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) B01D 53/50 B01D 53/34 B01D 53/77 B01D 53/81

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 酸化マグネシウムを吸収剤として使用す
る排煙脱硫装置において、酸化マグネシウムの粉体を直
接煙道ガス中に噴霧し同酸化マグネシウムの一部により
煙道ガス中に含まれるSO3 ガスを固気反応させる酸化
マグネシウム噴霧手段、ならびに同噴霧手段の後流に配
設され前記酸化マグネシウムの粉体および前記酸化マグ
ネシウムとSO3 との反応生成物を循環液で捕集すると
共に同循環液でSO2 ガスを気液反応で吸収する湿式の
吸収塔を有することを特徴とする酸化マグネシウムによ
る湿式排煙脱硫装置。
In a flue gas desulfurization apparatus using magnesium oxide as an absorbent, a powder of magnesium oxide is directly sprayed into a flue gas, and SO 3 gas contained in the flue gas by a part of the magnesium oxide is used. Spraying means for causing a solid-gas reaction of the magnesium oxide powder, and a circulating liquid for collecting the magnesium oxide powder and a reaction product of the magnesium oxide and SO 3 and being disposed downstream of the spraying means. A wet flue gas desulfurization apparatus using magnesium oxide, comprising a wet absorption tower for absorbing SO 2 gas by a gas-liquid reaction.
【請求項2】 前記吸収塔内における酸化を抑制し前記
循環液中に一定以上の亜硫酸イオンを確保する酸化抑制
手段を設けたことを特徴とする請求項1記載の酸化マグ
ネシウムによる湿式排煙脱硫装置。
2. The wet flue gas desulfurization using magnesium oxide according to claim 1, further comprising oxidation suppression means for suppressing oxidation in the absorption tower and securing a certain amount or more of sulfite ions in the circulating liquid. apparatus.
【請求項3】 前記酸化マグネシウムの注入量を排ガス
中のSO2 濃度、煙道ガスの流量、及び吸収塔内の液の
PH値を基に制御することを特徴とする請求項1又は2
記載の装置による湿式排煙脱硫方法。
3. The method according to claim 1, wherein the injection amount of the magnesium oxide is controlled based on the SO 2 concentration in the exhaust gas, the flow rate of the flue gas, and the PH value of the liquid in the absorption tower.
A wet flue gas desulfurization method using the apparatus described in the above.
JP5171457A 1993-02-26 1993-07-12 Wet flue gas desulfurization apparatus using magnesium oxide and desulfurization method thereof Expired - Fee Related JP2994913B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP5171457A JP2994913B2 (en) 1993-07-12 1993-07-12 Wet flue gas desulfurization apparatus using magnesium oxide and desulfurization method thereof
TW083106138A TW306885B (en) 1993-02-26 1994-07-05
ITRM940444A IT1272321B (en) 1993-07-12 1994-07-08 "PROCESS AND FUME DESULPHATION PLANT"
CN94108254A CN1048188C (en) 1993-07-12 1994-07-12 Flue gas desulfurization method and system
KR1019940016701A KR0125122B1 (en) 1993-07-12 1994-07-12 Flue gas desulfurization method and system

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5171457A JP2994913B2 (en) 1993-07-12 1993-07-12 Wet flue gas desulfurization apparatus using magnesium oxide and desulfurization method thereof

Publications (2)

Publication Number Publication Date
JPH0724252A JPH0724252A (en) 1995-01-27
JP2994913B2 true JP2994913B2 (en) 1999-12-27

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KR (1) KR0125122B1 (en)
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KR100905746B1 (en) * 2007-07-10 2009-07-01 에이취아이엠테크(주) Composition comprising micro particle of magnesium oxide for desulfurizating flue gas
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Also Published As

Publication number Publication date
CN1048188C (en) 2000-01-12
JPH0724252A (en) 1995-01-27
ITRM940444A1 (en) 1996-01-08
CN1102357A (en) 1995-05-10
KR950002840A (en) 1995-02-16
ITRM940444A0 (en) 1994-07-08
IT1272321B (en) 1997-06-16
KR0125122B1 (en) 1997-11-27

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