JPS5939328A - Desulfurization of exhaust gas - Google Patents

Desulfurization of exhaust gas

Info

Publication number
JPS5939328A
JPS5939328A JP57147799A JP14779982A JPS5939328A JP S5939328 A JPS5939328 A JP S5939328A JP 57147799 A JP57147799 A JP 57147799A JP 14779982 A JP14779982 A JP 14779982A JP S5939328 A JPS5939328 A JP S5939328A
Authority
JP
Japan
Prior art keywords
gas
exhaust gas
slurry
ejector
absorption
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
JP57147799A
Other languages
Japanese (ja)
Inventor
Tsukasa Nishimura
西村 士
Hiromitsu Asano
浅野 廣満
Shigeru Nozawa
野沢 滋
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 Power Ltd
Original Assignee
Babcock Hitachi 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 Babcock Hitachi KK filed Critical Babcock Hitachi KK
Priority to JP57147799A priority Critical patent/JPS5939328A/en
Publication of JPS5939328A publication Critical patent/JPS5939328A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To attain to reduce utility and to simplify an installation, by a method wherein an absorbing liquid withdrawn from an absorbing process is guided to an ejector and subjected to gas-liquid contact with the part of exhaust gas containing sulfur dioxide gas and oxygen. CONSTITUTION:Exhaust gas 101 is guided to a dust removing tower 1 to be introduced into an absorbing tower 3 and sulfur oxide in the exhaust gas 101 is absorbed and removed by a calcium type absorbent slurry 22. The reaction slurry is guided to an ejector 8 and the gas 33 from which dust is removed in the dust removing tower is absorbed with said slurry 22 passing through the ejector 8. In this case, the unreacted absorbent in the reaction slurry is reacted with SO2 in the gas to be converted to sulfite which is, in turn, oxidized by O2 in the gas along with sulfite formed in the absorbing process to be converted to sulfate.

Description

【発明の詳細な説明】 本発明は排ガス脱硫方法に係り、特に排ガスの除しん後
のガスを利用して吸収液スラリの反応および酸化を行な
い、硫酸塩を回収する湿式排ガス脱硫方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an exhaust gas desulfurization method, and more particularly to a wet exhaust gas desulfurization method for recovering sulfates by reacting and oxidizing an absorbent slurry using gas after exhaust gas removal.

湿式脱硫プロセスは、一般に°γルカリ金属、アルカリ
土類金属等の水酸化物、炭酸塩棟たけ酸化物の溶液もし
くは懸濁液を用いて、ガス中の硫黄酸化物を吸収、除去
し、副生品として石膏のような硫酸塩を得るものである
The wet desulfurization process generally uses solutions or suspensions of hydroxides and carbonate oxides of alkali metals, alkaline earth metals, etc. to absorb and remove sulfur oxides from gases, and As a raw product, sulfate like gypsum is obtained.

第1図は、アルカリ剤としてカルシウム(C−)系吸収
剤を用いて硫酸カルシウム(石膏)を副生、回収する従
来の脱硫プロセスの典型例を示したもである。図におい
て、ボイラ等の排ガス、1o1は除じん塔人ログク)3
1から除しん塔1に導びかれ、除じん、冷却された後、
飛散ミストはミストエリミネータ2・により除去され、
吸収塔3でカルシウム系吸収剤スラリ22により、排ガ
ス101中の硫黄酸化物が吸収除去された後、清浄ガス
102はダクト32を通1−て排出される。硫黄酸化物
を吸収したカルシウム系吸収剤22は吸収塔3訃よび吸
収塔循環タンク5内で亜硫酸カルシウムとな抄、一部は
排ガス中の酸素により酸化されて石膏となり、一部は未
反応吸収剤としてスラリ中に残存する。この反応スラリ
はプリードボンプフにより導管13を介して反応槽9へ
供給され、未反応吸収剤は硫酸23を添加され、酸化に
好適なpHに調整される。次に一部生成した石膏を含む
スラリは導管15によシ酸化塔10に供給され、ここで
亜硫酸カルシウムは空気酸化され、さらにシラフナ11
へ供給され、固液分離された後、固形物スラリは2、遠
心分離機20で脱水され、石膏が回収される。一方、固
液分離および脱水時の濾過水は循環、再使用される。
FIG. 1 shows a typical example of a conventional desulfurization process in which calcium sulfate (gypsum) is produced as a by-product and recovered using a calcium (C-) based absorbent as an alkaline agent. In the figure, exhaust gas from boilers, etc., 1o1 is the dust removal tower log) 3
1 to the dust removal tower 1, where it is removed and cooled,
The scattered mist is removed by the mist eliminator 2.
After sulfur oxides in the exhaust gas 101 are absorbed and removed by the calcium-based absorbent slurry 22 in the absorption tower 3, the clean gas 102 is discharged through the duct 32. The calcium-based absorbent 22 that has absorbed sulfur oxides is converted into calcium sulfite in the absorption tower 3 and the absorption tower circulation tank 5. Part of it is oxidized by oxygen in the exhaust gas and becomes gypsum, and part of it is unreacted and absorbed. It remains in the slurry as an agent. This reaction slurry is supplied to the reaction tank 9 via a conduit 13 by a pre-de-bonpf, and the unreacted absorbent is added with sulfuric acid 23 to adjust the pH to a suitable value for oxidation. The partially produced slurry containing gypsum is then fed via conduit 15 to the silica oxidation tower 10, where the calcium sulfite is air oxidized and further
After solid-liquid separation, the solid slurry is dehydrated in a centrifugal separator 20 and gypsum is recovered. On the other hand, filtrate water during solid-liquid separation and dehydration is recycled and reused.

1、かじながら、このような従来技術では、吸収工程か
ら抜き出されるスラリ中の亜硫酸塩の酸化にあたり、ス
ラリ中の未反応の吸収剤を反応させ、酸化に適したpH
にするため硫酸を添加し、またスラリ中の亜硫酸塩の酸
化に空気を使用しているため、これらのユーティリティ
と設備が必要となる。
1. However, in this conventional technology, when oxidizing sulfite in the slurry extracted from the absorption process, the unreacted absorbent in the slurry is reacted, and the pH is adjusted to a pH suitable for oxidation.
These utilities and equipment are required because sulfuric acid is added to oxidize the slurry and air is used to oxidize the sulfite in the slurry.

本発明の目的は、上記した従来技術の欠点をなくシ、吸
収工程から抜き出された吸収液中の未反応の吸収剤の反
応に硫酸を使用したり、吸収液中の亜硫酸塩の酸化に空
気を使用することなく、副生品である石膏を回収するこ
とができる湿式脱硫プロセスを提供するものである。
The purpose of the present invention is to eliminate the above-mentioned drawbacks of the prior art, and to use sulfuric acid for the reaction of unreacted absorbent in the absorbent extracted from the absorption process and for the oxidation of sulfite in the absorbent. The present invention provides a wet desulfurization process that can recover gypsum as a byproduct without using air.

本発明は、吸収工程から抜き出された吸収液と、除しん
塔で除じんした後の亜硫酸ガス(S 02)および酸素
(02)を含有する排ガスをエゼクタを用いて気液接触
させ、排ガス中の802によって未反応吸収剤を亜硫酸
塩とし、さらに排ガス中の02によって硫酸塩(石膏)
とするようにした亀のである。
The present invention uses an ejector to bring the absorption liquid extracted from the absorption process into gas-liquid contact with the exhaust gas containing sulfur dioxide gas (S 02) and oxygen (02) after removing dust in a dust removal tower, so that the exhaust gas The 802 inside converts the unreacted absorbent into sulfite, and the 02 in the exhaust gas converts it into sulfate (gypsum).
It is a turtle that was made to look like this.

本発明においては、除しん後の排ガスをエゼクタで吸収
液と接触させることが重要である。石炭焚ボイラ等の排
ガスは、ばいじんが多く、また、H(1、HFなどのハ
ロゲン化物を含むので、除じん前の排ガス中の802に
よって、吸収液のpH調整をおこなうことは、副生石膏
の品質を低下させるばかりでなく、機器の材料の腐食に
も影響を及ばずことになる。従ってこれらダストや)1
0ゲン化物を除しん塔で除去した後のSO2,02を含
有したガスを吸収液と接触させることが、良品質の石膏
を得る上で重要である。
In the present invention, it is important to bring the exhaust gas after dust removal into contact with the absorption liquid in the ejector. Exhaust gas from coal-fired boilers, etc., contains a lot of dust and halides such as H(1, HF), so adjusting the pH of the absorption liquid with 802 in the exhaust gas before dust removal is a good way to prevent by-product gypsum. This will not only reduce the quality but also affect the corrosion of the equipment's materials.Thus, these dusts and
It is important to contact the gas containing SO2,02 with the absorption liquid after removing the 0-genides in the scrubbing tower in order to obtain high-quality gypsum.

以下、本発明を図面によりさらに詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to the drawings.

第2図は、本発明の湿式排ガス脱偕方法の一実施例を示
すフローシートである。ボイラ等の排ガス101は、除
じん塔入ロダクト31から除じん塔lに導びかれ、ここ
で除しん、冷却された後、飛散ミストをミストエリミネ
ータ2により除去し、吸収塔3に導水され、ここでカル
シウム系吸収剤スラリ22により、排ガス10”l中の
硫黄酸化物が吸収除去される。吸収塔3の塔頂ダクト3
2から清浄ガス102が排出される。硫黄酸化物を吸収
したカルシウム系吸収剤゛22は吸収塔3および吸収塔
循環タンク5内で亜硫酸塩となり、一部は排ガス中の酸
素により、酸化されて、石膏となり、一部は未反応吸収
剤としてスラリ中に残存する。
FIG. 2 is a flow sheet showing an embodiment of the wet exhaust gas degassing method of the present invention. Exhaust gas 101 from a boiler or the like is led from a dust removal tower input rod duct 31 to a dust removal tower 1, where it is removed and cooled, after which scattered mist is removed by a mist eliminator 2, and water is led to an absorption tower 3. Here, the calcium-based absorbent slurry 22 absorbs and removes sulfur oxides in 10"l of exhaust gas. The top duct 3 of the absorption tower 3
Clean gas 102 is discharged from 2. The calcium-based absorbent 22 that has absorbed sulfur oxides becomes sulfite in the absorption tower 3 and the absorption tower circulation tank 5, and some of it is oxidized by oxygen in the exhaust gas and becomes gypsum, and some of it is unreacted and absorbed. It remains in the slurry as an agent.

この反応液スラリは、ブリードポンプ7によって昇圧さ
れ導管13によりエゼクタ8に導びかれる。
This reaction liquid slurry is pressurized by the bleed pump 7 and guided to the ejector 8 through the conduit 13.

エゼクタ8に供給された反応液スラリは、エゼクタ内を
通過する際に、除じん塔で除じんした後のガス33が吸
引される。この際、ガス中のS02により、反応スラリ
中の未反応の吸収剤が反応して亜硫酸塩となり、この亜
硫酸塩は、吸収工程で生成された亜硫酸塩とともに、該
ガス中の02によし酸化されて硫酸塩となる。この際の
酸化性能は、従来の酸化塔アトマイザによる空気酸化に
比べてはるかに良好であるため、酸素量は、ボイラ等の
排ガス中の0.で充分であるが、排ガス中の02濃度が
低い場合、または酸化速度を更に高める必要がある場合
には、排ガスの一部にライン36から空気を吹き込むこ
とにより、酸化速度を高くすることができる。
When the reaction liquid slurry supplied to the ejector 8 passes through the ejector, the gas 33 after dust removal in the dust removal tower is sucked. At this time, the unreacted absorbent in the reaction slurry reacts with S02 in the gas to become sulfite, and this sulfite is oxidized by 02 in the gas together with the sulfite generated in the absorption process. It becomes sulfate. The oxidation performance in this case is much better than air oxidation using a conventional oxidation tower atomizer, so the amount of oxygen in the exhaust gas from the boiler, etc. However, if the 02 concentration in the exhaust gas is low or if the oxidation rate needs to be further increased, the oxidation rate can be increased by blowing air into part of the exhaust gas from the line 36. .

エゼクタ8で反応、酸化して、硫酸塩と々つだスラリは
、導管16を経てシラフナ11に送られ、ここで固液分
離がおこなわれ、固形物スラリは導管18から脱水機2
0に送られ、ここで脱水されて硫酸塩の粒子状体(石膏
)40として回収される。シラフナ11は、固液分離と
同時に気液分離をおこなうような構造とすることが望ま
しい。シラフナ11で分離されたガスを導管34を経て
吸収塔3に戻せば、特別な処理を要することなく、シス
テムを簡素化することができる。シラフナ11の濾過水
は導v19により取り出され、元の装置に再循環使用さ
れる。
The slurry reacted and oxidized in the ejector 8 and containing a lot of sulfate is sent to the Shirafuna 11 through the conduit 16, where solid-liquid separation is performed, and the solid slurry is passed through the conduit 18 to the dehydrator 2.
0, where it is dehydrated and recovered as sulfate particles (gypsum) 40. It is desirable that the Shirafuna 11 has a structure that performs gas-liquid separation at the same time as solid-liquid separation. By returning the gas separated by the Shirafuna 11 to the absorption tower 3 via the conduit 34, the system can be simplified without requiring any special treatment. The filtered water of the Shirafuna 11 is taken out by a conduit 19 and recycled to the original device.

次に、本発明の具体的実施例をあげて説明する。Next, specific examples of the present invention will be described.

第2図のフローシートによる実施態様におりて、除じん
塔入口排ガスfi13,0OON+n”/h、入口SO
□濃度1,000p、ガス中のH2O: 10 Voj
2%、02:6Voj2%で運転している湿式石灰石−
石膏法脱硫装置において、吸゛収工程から抜き出された
反応液スラリ中の未反応炭酸カルシウムは約59f)で
あったが、このスラリをエゼクタに導びき、除しん塔で
除じんした後の排ガス150 N+++’ / hをエ
ゼクタで吸引して反応させた結果、吸収工程の反応液ス
ラリから99゜6%の純度の石膏が回収された。
In the embodiment according to the flow sheet of FIG. 2, the dust removal tower inlet exhaust gas fi13,0OON+n"/h,
□Concentration 1,000p, H2O in gas: 10 Voj
Wet limestone operating at 2%, 02:6 Voj2% -
In the gypsum method desulfurization equipment, unreacted calcium carbonate in the reaction liquid slurry extracted from the absorption process was approximately 59 f), but after this slurry was led to the ejector and dust removed in the dust removal tower, As a result of suctioning exhaust gas of 150 N+++'/h with an ejector and causing a reaction, gypsum with a purity of 99.6% was recovered from the reaction liquid slurry of the absorption step.

以上、本発明によれば、排ガス中のS02.02によっ
て、吸収液をエゼクタ内で亜硫酸塩の生成と液のpH調
整および硫酸塩への酸化がおこなわれるため、従来の硫
酸によるpHFJ整タンクやアトマイザを有する酸化塔
が不要になり、ユーティリティの低減および設備の簡素
化を図ることができる。また、エゼクタで反応、酸化し
だスラリは、シラフナで固液分離して良質の副生石膏を
回収することができ、さらにシラフナでエゼクタの同伴
ガスを気液分離して吸収塔に戻すことにより、特別なガ
ス処理装置が不要となり、システム全体の合理化を図る
ことができる。
As described above, according to the present invention, S02.02 in the exhaust gas generates sulfite, adjusts the pH of the liquid, and oxidizes the absorption liquid to sulfate in the ejector. An oxidation tower having an atomizer is no longer necessary, and utilities can be reduced and equipment simplified. In addition, the slurry that reacts and oxidizes in the ejector can be separated into solid and liquid using Shirafuna to recover high-quality byproduct gypsum.Furthermore, by separating the accompanying gas from the ejector into gas and liquid using Shirafuna and returning it to the absorption tower, No special gas processing equipment is required, and the entire system can be streamlined.

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

第1図は、従来の湿式脱硫プロセスのフローシート、第
2図は、本発明の一実施例を示す湿式脱硫プロセスのフ
ローシートである。 1・・・・・・除じん塔、2・・・・・・ミストエリミ
ネータ、3・・・・・・吸収塔、4・・・・・・デミス
タ、5・・・・・・吸収塔循環タンク、6・・・・・・
循環ポンプ、9・・・・・・ブリードポンプ、8・・・
・・・エゼクタ1,11・・・・・・シラフナ。
FIG. 1 is a flow sheet of a conventional wet desulfurization process, and FIG. 2 is a flow sheet of a wet desulfurization process showing an embodiment of the present invention. 1... Dust removal tower, 2... Mist eliminator, 3... Absorption tower, 4... Demister, 5... Absorption tower circulation Tank, 6...
Circulation pump, 9... Bleed pump, 8...
...Ejecta 1, 11...Shirafuna.

Claims (1)

【特許請求の範囲】 (1)排ガスを吸収液と接触させて該ガス中の硫黄酸化
物を吸収、除去する吸収工程を有する排ガス脱硫方法に
おいて、吸収工程から抜出される吸収液をエゼクタに導
びき、除しん塔で除じんしfc稜の亜砧酸ガス、酸素を
含有する排ガスの一部を気液接触させて、吸収液中の未
反応吸収剤、並置酸塩を反応、酸化して硫酸塩とするこ
とを特徴とする排ガス脱硫方法。 (2、特許請求の範囲第1項において、排ガス中の一部
に空気を吹き込むことを特徴とする排ガス脱硫方法。 (3)特許請求の範囲第1項または第2項において、硫
酸塩の分離工程を含むことを特徴とする排ガス脱硫方法
。 (4)特許請求の範囲第1項ない17第3項のいずれか
において、エゼクタの同伴ガスを気液分離して得られた
ガスを吸収工程に戻すことを特徴とする排ガス脱硫方法
[Scope of Claims] (1) In an exhaust gas desulfurization method having an absorption process in which exhaust gas is brought into contact with an absorption liquid to absorb and remove sulfur oxides in the gas, the absorption liquid extracted from the absorption process is introduced to an ejector. A part of the exhaust gas containing arsenic acid gas and oxygen from the fc ridge is brought into gas-liquid contact to react and oxidize the unreacted absorbent and juxtaposed acid salts in the absorption liquid. An exhaust gas desulfurization method characterized by using sulfate. (2. In claim 1, the exhaust gas desulfurization method is characterized by blowing air into a part of the exhaust gas. (3) In claim 1 or 2, separation of sulfate (4) In any one of claims 1 to 17, claim 3, the gas obtained by gas-liquid separation of the gas entrained in the ejector is subjected to an absorption step. An exhaust gas desulfurization method characterized by returning the gas.
JP57147799A 1982-08-27 1982-08-27 Desulfurization of exhaust gas Pending JPS5939328A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57147799A JPS5939328A (en) 1982-08-27 1982-08-27 Desulfurization of exhaust gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57147799A JPS5939328A (en) 1982-08-27 1982-08-27 Desulfurization of exhaust gas

Publications (1)

Publication Number Publication Date
JPS5939328A true JPS5939328A (en) 1984-03-03

Family

ID=15438471

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57147799A Pending JPS5939328A (en) 1982-08-27 1982-08-27 Desulfurization of exhaust gas

Country Status (1)

Country Link
JP (1) JPS5939328A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6342720A (en) * 1986-08-07 1988-02-23 Mitsubishi Heavy Ind Ltd Wet flue gas desulfurization method
CN104624020A (en) * 2015-03-11 2015-05-20 北京化工大学常州先进材料研究院 Method for removing hydrogen sulphide and solid dust in gas
GB2555083A (en) * 2016-10-03 2018-04-25 Ge Energy Power Conversion Technology Ltd Methods of space cooling

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6342720A (en) * 1986-08-07 1988-02-23 Mitsubishi Heavy Ind Ltd Wet flue gas desulfurization method
CN104624020A (en) * 2015-03-11 2015-05-20 北京化工大学常州先进材料研究院 Method for removing hydrogen sulphide and solid dust in gas
GB2555083A (en) * 2016-10-03 2018-04-25 Ge Energy Power Conversion Technology Ltd Methods of space cooling

Similar Documents

Publication Publication Date Title
EP0620187B1 (en) Process for the simultaneous absorption of sulfur oxides and production of ammonium sulfate
US4452766A (en) Double alkali process for removal of sulfur dioxide from gas streams
JP5000557B2 (en) Wet flue gas desulfurization equipment
JPH0536085B2 (en)
US5645807A (en) Magnesium-enhanced sulfur dioxide scrubbing with gypsum formation
JPH09502651A (en) Hydrogen sulfide absorption method and equipment
JP4524914B2 (en) Wet flue gas desulfurization equipment
JPS5939328A (en) Desulfurization of exhaust gas
US3650692A (en) Removal of sulfur dioxide from waste gases
JPS62225226A (en) Wet stack-gas desulfurization facility
US5614158A (en) Process for removing sulfur dioxide from gases and producing gypsum and purified magnesium hydroxide
US3935296A (en) Method for removing sulfur dioxide from a combustion exhaust gas
JPS5939327A (en) Wet type desulfurization of exhaust gas
JPH04346816A (en) Treatment of exhaust gas
US4313924A (en) Process for removal of sulfur dioxide from gas streams
JPH07114918B2 (en) Wet Flue Gas Desulfurization Method
US3870781A (en) Air pollution control system
JP2020089804A (en) Detoxification method of exhaust gas containing sulfur dioxide
JP3645675B2 (en) Exhaust gas desulfurization method
US3600131A (en) Removal of sulfur dioxide from waste gases
JPS6261620A (en) Wet waste gas desulfurization method
JPS6094117A (en) Wet desulfurizer
JPH055528B2 (en)
JP4192319B2 (en) Wet flue gas desulfurization method and wet flue gas desulfurization apparatus
JPH10118452A (en) Removal of sulfur dioxide and nitrogen oxide from combustion gas