JPS60132626A - Removal of gaseous mercury in wet exhaust gas scrubbing equipment - Google Patents

Removal of gaseous mercury in wet exhaust gas scrubbing equipment

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Publication number
JPS60132626A
JPS60132626A JP58242531A JP24253183A JPS60132626A JP S60132626 A JPS60132626 A JP S60132626A JP 58242531 A JP58242531 A JP 58242531A JP 24253183 A JP24253183 A JP 24253183A JP S60132626 A JPS60132626 A JP S60132626A
Authority
JP
Japan
Prior art keywords
exhaust gas
mercury
gaseous mercury
caustic soda
gas
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
JP58242531A
Other languages
Japanese (ja)
Inventor
Kenji Kaketa
健二 掛田
Hiroichi Obata
小畑 博一
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.)
Hitachi Zosen Corp
Original Assignee
Hitachi Zosen Corp
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 Hitachi Zosen Corp filed Critical Hitachi Zosen Corp
Priority to JP58242531A priority Critical patent/JPS60132626A/en
Publication of JPS60132626A publication Critical patent/JPS60132626A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To remove gaseous mercury in exhaust gas along with HCl and SOx with high efficiency, by scrubbing exhaust gas with an alkali solution to which thiourea and cuprous chloride are added. CONSTITUTION:Caustic soda 5, to which thiourea 2 and cuprous chloride 3 are added, is supplied to a gas scrubbing tower 13 while the exhaust gas 6 of a garbage incinerator is guided to said scrubbing tower 13 to be scrubbed with caustic sode 5. HCl and SOx in the exhaust gas are removed and, at the same time, 90% or more of gaseous mercury is removed. Purified exhaust gas is exhausted through a re-heater 25 while mixed with heated air 19.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は湿式洗煙設備でのガス状水銀の除去方法に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method for removing gaseous mercury in wet smoke cleaning equipment.

従来例の構成とその問題点 最近、こみ焼却プラントの排ガス中に含まれる重金属類
、特に沸点の低い水銀含有量が大きな環境問題となって
来ている(水銀はごみ中の例えば乾電池2体温計、蛍光
灯等に含まれている。)。しかしながら、従来のベンチ
ュリースクラバーやトレー、充填塔等で構成される湿式
洗煙設備ではアルカリ溶液(Na01(、Ca(OH)
z−CaCO5等)による水銀除去率(ばいじん中子ガ
ス中)は、設備入口水銀量に対し60〜80%であり、
未だ不十分なものであった。
Conventional structure and problems Recently, heavy metals contained in waste gas from waste incineration plants, especially the content of mercury, which has a low boiling point, have become a major environmental problem (mercury is found in waste, such as thermometers with two dry batteries, etc.). (Included in fluorescent lights, etc.) However, in conventional wet smoke cleaning equipment consisting of Venturi scrubbers, trays, packed towers, etc., alkaline solutions (Na01(, Ca(OH))
The mercury removal rate (in soot and dust core gas) by z-CaCO5, etc. is 60 to 80% of the amount of mercury at the equipment inlet,
It was still inadequate.

発明の目的 本発明は上記従来の欠点を解消する湿式洗煙設備でのガ
ス状水銀の除去方法を提供することを目的とする。
OBJECTS OF THE INVENTION It is an object of the present invention to provide a method for removing gaseous mercury in wet smoke cleaning equipment, which eliminates the above-mentioned conventional drawbacks.

発明の構成 上記目的を達成するため、本発明の湿式洗煙設備でのガ
ス状水銀の除去方法は、チオ尿素と塩化第1銅を添加し
たアルカリ溶液で排ガスを湿式洗煙する構成としたもの
であり、これにより、脱塩化水素(HCI)、脱硫黄酸
化物(SOx)と同時にガス状水銀を約90%以上除去
することができるものである。
Structure of the Invention In order to achieve the above object, the method for removing gaseous mercury using wet smoke cleaning equipment of the present invention is configured to perform wet smoke cleaning of exhaust gas with an alkaline solution to which thiourea and cuprous chloride are added. This makes it possible to remove about 90% or more of gaseous mercury at the same time as dehydrochlorination (HCI) and desulfurization oxides (SOx).

実施例と作出 以下、本発明の一実施例を図面に基づいて説明する。Examples and production Hereinafter, one embodiment of the present invention will be described based on the drawings.

第1図は本発明方法を適用するための湿式洗煙設備の全
体を示す。図において、(1)は苛性ソーダタンクで、
チオ尿素(SC(NHz)2) (2)と塩化第1銅(
CuCl X3)および希釈水(4)を添加されtこ苛
性ソーダ(5)が入れられている。(0)は該苛性ソー
ダタンク(1)から苛性ソーダ(5)を引出す苛性ソー
ダポンプ、(7)は該苛性ソーダポンプ(6)によって
送られて来た苛性ソーダ(5)および温水槽(8)に溜
められた苛性ソーダ(5)を冷却塔(9)に送る温水ポ
ンプで、冷却塔(9)で冷却された苛性ソーダ(5)は
冷水槽00に送られる構成とされている。(1ηは冷水
槽αQに適宜供給される補給水である。(2)は冷水槽
Of3の苛性ソーダ(5)を引出してガス洗浄塔(至)
の減湿部0尋に供給する冷水ポンプで、減湿部a→で使
用された苛性ソーダ(5)は前記温水槽(8)に戻され
る構成とされている。なお、前記温水ポンプ(8)から
冷却塔(9)に送られる苛性ソーダ(5)の一部はガス
洗浄塔α椴の冷却部(ハ)に供給される構成とされてい
る。
FIG. 1 shows the entire wet smoke cleaning equipment for applying the method of the present invention. In the figure, (1) is a caustic soda tank;
Thiourea (SC(NHz)2) (2) and cuprous chloride (
CuCl (X3) and dilution water (4) are added to the caustic soda (5). (0) is a caustic soda pump that draws out caustic soda (5) from the caustic soda tank (1), and (7) is the caustic soda (5) sent by the caustic soda pump (6) and stored in the hot water tank (8). The hot water pump sends caustic soda (5) to a cooling tower (9), and the caustic soda (5) cooled by the cooling tower (9) is sent to a cold water tank 00. (1η is the make-up water that is supplied to the cold water tank αQ as needed. (2) is the water that draws out the caustic soda (5) from the cold water tank Of3 and sends it to the gas scrubbing tower.
The cold water pump is configured to supply caustic soda (5) used in the dehumidification section a→ to the hot water tank (8). A portion of the caustic soda (5) sent from the hot water pump (8) to the cooling tower (9) is supplied to the cooling section (c) of the gas cleaning tower α.

一方、0Qはごみ焼却炉αηからガス洗浄塔α葎の冷却
部a→に供給された焼却炉排ガス、a枠はガス洗浄塔(
至)の上端から出た焼却炉排ガスα・と加熱空気α呻と
を混合する空気ガス混合器、で、該空気ガス混合器[相
]に供給される加熱空気Onは、空冷板レンガ(ホ)か
らの加熱空気(ハ)を白煙防止用空気加熱器(ホ)で蒸
気(2)と熱交換させたものが用いられる。なお、(ハ
)はドレンである。に)は空気ガス混合器(2)で空気
と混合された排ガスDIを蒸気(ホ)と熱交換させて再
加熱するガス再加熱器で、該ガス再加熱器に)を通った
排ガスaQは煙突(ロ)に導かれる構成とされている。
On the other hand, 0Q is the incinerator exhaust gas supplied from the waste incinerator αη to the cooling section a→ of the gas cleaning tower α, and the a frame is the gas cleaning tower (
An air-gas mixer that mixes incinerator exhaust gas α and heated air α emitted from the upper end of the air-cooled plate brick ( The heated air (c) from ) is heat-exchanged with steam (2) in an air heater for white smoke prevention (e). Note that (c) is a drain. (2) is a gas reheater that reheats the exhaust gas DI mixed with air in the air-gas mixer (2) by exchanging heat with steam (E).The exhaust gas aQ that has passed through the gas reheater (2) is It is said to be guided to the chimney (b).

なお、に)はドレンである。In addition, 2) is a drain.

(2)はガス洗浄塔(至)内の苛性ソーダ(5)を循環
させる冷却液循環ポンプで、循環経路の途中には前記苛
性ソーダポンプ(6)から苛性ソーダ(5)が適宜供給
される構成とされている。また、循環経路の途中から適
宜苛性ソーダ(5)を引出して洗煙排材処理装置…に導
く構成とされている。のりはガス洗浄塔(至)の底部か
ら苛性ソーダ(5)を引出す排液ポンプ、eカは該排液
ポンプ(81)から供給された苛性ソーダ(5)を固液
分離する液体サイクロンで、分離再生した苛性ソーダ(
5)はガス洗浄塔(至)の冷却部(至)に戻され、排材
(財)は洗煙排材処理装置に)に導かれる構成とされて
いる。
(2) is a coolant circulation pump that circulates caustic soda (5) in the gas scrubbing tower (to), and the caustic soda (5) is appropriately supplied from the caustic soda pump (6) to the middle of the circulation path. ing. Further, the structure is such that the caustic soda (5) is appropriately drawn out from the middle of the circulation path and guided to the smoke cleaning exhaust material processing device. Nori is a drainage pump that draws out caustic soda (5) from the bottom of the gas scrubbing tower (to), and e is a liquid cyclone that separates the caustic soda (5) supplied from the drainage pump (81) into solid and liquid, and performs separation and regeneration. Caustic soda (
5) is returned to the cooling section (to) of the gas cleaning tower (to), and the waste material is guided to the smoke washing waste material processing device.

このような構成の湿式洗煙設備において、ガス洗浄塔(
至)にチオ尿素(2)と塩化第1銅(3)を添加した苛
性ソーダ(5)を供給することにより、焼却炉排ガスa
1の脱塩化水素および脱硫黄酸化物が行うことができ、
またこれと同時にガス状水銀を約90%以上除去するこ
とができる。
In wet smoke cleaning equipment with such a configuration, a gas cleaning tower (
By supplying caustic soda (5) containing thiourea (2) and cuprous chloride (3) to
1 dehydrochlorination and desulfurization oxides can be carried out,
At the same time, more than 90% of gaseous mercury can be removed.

次に、これを2つの実験例に基づいて具体的に説明する
Next, this will be specifically explained based on two experimental examples.

第2図は第1の実験(室内テスト)に用いたテスト装置
を示す。図において、(8→は吸収びん、(80は該吸
収びん(財)で発生したガス状水銀の循環ラインで、該
循環ライン(86)の途中に、第1切替コック働、乾燥
剤(イ)、吸光セル(88) 、ダイヤフラムポンプ(
89) 、第2切替コツク(鉤が順番に設けられている
FIG. 2 shows the test equipment used in the first experiment (indoor test). In the figure, (8→ is an absorption bottle, (80 is a circulation line for gaseous mercury generated in the absorption bottle), and in the middle of the circulation line (86) there is a first switching cock, a desiccant ), absorption cell (88), diaphragm pump (
89), second switching hook (hooks are provided in order).

(4υは吸光セル(38)の−側に設けられた分光測定
器、(6)はその記録計、(至)は吸光セル(88)の
他側に設けられた水銀ランプである。すなわち、本テス
ト装置は、還元気化法による原子〆吸光測定装置を用い
たものである。
(4υ is a spectrometer installed on the - side of the absorption cell (38), (6) is its recorder, and (to) is a mercury lamp installed on the other side of the absorption cell (88). That is, This test device uses an atomic absorption spectrometry device using the reductive vaporization method.

このようなテスト装置において、先ず、吸収びん(財)
の中に塩化第2水銀溶液(水銀としてo、ooo5q)
を入れ、さらに塩化第1すず溶液を加えて直ちにダイヤ
フラムポンプφのを作動させる。そうすると、水中の水
銀イオンは塩化第1すすによって金属水銀まで還元気化
され、ガス状水銀として循環ライン(至)を循環する。
In such a test device, first, an absorption bottle (goods) is used.
mercuric chloride solution (o, ooo5q as mercury)
, then add the stannous chloride solution and immediately operate the diaphragm pump φ. Then, the mercury ions in the water are reduced and vaporized by the soot chloride to metallic mercury, which circulates through the circulation line as gaseous mercury.

そこで、記録計(6)を見ながら十分還元が進行したと
ころで切替コック+aft)(40)でガス状水銀を種
々の吸収液の入った吸収びんに切替え、水銀の吸収を行
なった。吸収液の種類は第1表の室内テスト結果に示す
通り、脱硝剤成分のチオ尿素およびその他の成分との組
合せ(PH中性)について行い、純水および過マンガン
酸カリウム−硫酸液での吸収率と比較した。なお、過マ
ンガン酸カリウム−硫酸液はガス状水銀の分析に使用さ
れている吸収液であり、吸収効率100%とされている
Therefore, while watching the recorder (6), when the reduction had sufficiently progressed, the gaseous mercury was switched to an absorption bottle containing various absorption liquids using the switching cock +aft (40), and the mercury was absorbed. As shown in the laboratory test results in Table 1, the type of absorption liquid was determined by combining the denitrification agent with thiourea and other ingredients (neutral pH), and absorption with pure water and potassium permanganate-sulfuric acid solution. compared with the rate. Note that the potassium permanganate-sulfuric acid solution is an absorption liquid used in the analysis of gaseous mercury, and is said to have an absorption efficiency of 100%.

このテスト結果から次のようなことが推察できる。The following can be inferred from this test result.

(1)チオ尿素と銅の共存する溶液が水銀の除去に効果
がある。
(1) A solution in which thiourea and copper coexist is effective in removing mercury.

(2)チオ尿素のみでは純水に比較して水銀の吸収性は
悪い。
(2) Thiourea alone has poor mercury absorption compared to pure water.

(3)チオ尿素と鉄の共存する溶液では、純水の場合と
同程度である。
(3) In a solution in which thiourea and iron coexist, it is about the same as in the case of pure water.

表 1 注1)加温処理65〜70℃は現場と同じ温度まで80
分間加温した。なお吸収テストは、水銀測定装置(原水
吸光光度針)への水蒸気による影響を避けるため放冷後
、実施した。
Table 1 Note 1) Heating treatment at 65-70℃ is heated to 80℃ to the same temperature as on-site.
Warmed for minutes. The absorption test was conducted after cooling to avoid the influence of water vapor on the mercury measuring device (raw water absorption spectrometer needle).

注2)ガス状水銀の吸収を開始させ、8分後の記録紙上
のピーク高さを処理ガス水銀濃度とし、吸収率を算出し
た。
Note 2) The absorption rate of gaseous mercury was calculated using the peak height on the recording paper after 8 minutes as the treated gas mercury concentration.

第8図は第2の実験(室外テスト)に用いたテスト装置
を示す。図において、■はごみ焼却炉■からの排ガス(
46)をポンプ(4’l)を通して供給される冷却塔、
■は該冷却塔(伸出の水酸化ナトリウム(NaOH)ま
たは炭酸カルシウム(CaC03) (49)を循環さ
せる循環ポンプ、(財)は冷却塔働)からの排ガス(財
)を供給されて該排ガス(4ψから塩化水素、硫黄酸化
物。
FIG. 8 shows the test equipment used in the second experiment (outdoor test). In the figure, ■ is the exhaust gas from the garbage incinerator ■ (
46) a cooling tower fed through a pump (4'l);
(2) is supplied with exhaust gas from the cooling tower (a circulation pump that circulates sodium hydroxide (NaOH) or calcium carbonate (CaC03) (49) from the cooling tower). (Hydrogen chloride, sulfur oxide from 4ψ.

水銀ヒユームを吸収する吸収塔、(51)は該吸収塔−
内のチオ尿素および塩化第1銅を添加された炭酸カルシ
ウムφのを循環させる循環ポンプ、(財)は吸収塔@)
を出た排ガス(46)を再加熱する再加熱器で、該再加
熱器(財)を通った排ガス(46)は煙突(ロ)に導か
れる構成とされている。すなわち、本テスト装置は従来
の湿式洗煙設備のガス冷却・ガス吸収液補給用の苛性ソ
ーダタンクにチオ尿素と塩化第1銅を添加して排ガス(
46)中のガス状水銀を除去しようとするものである。
An absorption tower for absorbing mercury fume, (51) is the absorption tower -
A circulation pump that circulates calcium carbonate φ to which thiourea and cuprous chloride have been added;
The exhaust gas (46) that has passed through the reheater is guided to the chimney (b). In other words, this test device adds thiourea and cuprous chloride to a caustic soda tank for gas cooling and gas absorption liquid replenishment in conventional wet smoke cleaning equipment.
46) It is intended to remove gaseous mercury in.

なお、図中、<A><B><C><D><E>はそれぞ
れ測定地点を示す。
In addition, in the figure, <A><B><C><D><E> indicate measurement points, respectively.

このようなテスト装置において、先ず、排ガス@6)は
冷却塔(→で増湿冷却され、水酸化ナトリウムまたは炭
酸カルシウム(49)により塩化水素が溶解・吸収され
る。そして、吸収塔(5Φでさらに塩化水素。
In such a test device, the exhaust gas @ 6) is humidified and cooled in the cooling tower (→), and hydrogen chloride is dissolved and absorbed by sodium hydroxide or calcium carbonate (49). Plus hydrogen chloride.

硫黄酸化物、水銀ヒユームが吸収される。第2表はこの
テスト結果を示す。
Sulfur oxides and mercury fume are absorbed. Table 2 shows the results of this test.

このテストから次のような結果が得られた。The following results were obtained from this test.

(1)装置全体での水銀除去率 86.6〜99.5%
(2)装置出口(7)水銀濃度 0.002〜0.08
1J/Nm(3)冷却塔での水銀除去率 71.8〜9
4.296(4)吸収塔での水銀除去率 62,2〜9
7.9%(5)冷却塔の吸収剤 NaOHとCaCO3
による水銀除去率はほとんど差がない。
(1) Mercury removal rate of the entire device 86.6-99.5%
(2) Equipment outlet (7) Mercury concentration 0.002 to 0.08
1J/Nm (3) Mercury removal rate in cooling tower 71.8-9
4.296(4) Mercury removal rate in absorption tower 62.2~9
7.9% (5) Cooling tower absorbent NaOH and CaCO3
There is almost no difference in the mercury removal rate.

(6)冷却塔及び吸収塔での循環量 循環量による水銀除去率はほとんど差がない。(6) Circulation amount in cooling tower and absorption tower There is almost no difference in the mercury removal rate depending on the amount of circulation.

(7)チオ尿素(SC(Nl2)+)の濃度濃度による
水銀除去率はほとんど差がない。
(7) Concentration of thiourea (SC(Nl2)+) There is almost no difference in the mercury removal rate depending on the concentration.

(8)吸収塔のもれだな段数 段数による水銀除去率はほとんど差がない。(8) Number of leakage stages of absorption tower There is almost no difference in the mercury removal rate depending on the number of stages.

したがって、第1と第2の実験の結果をまとめて考察す
ると、第2の実験において約90%以上の水銀除去率、
装置出口水銀濃度的0.O8fEf/Nd以下という処
理結果が得られたことから、チオ尿素・銅の共存する溶
液はガス状水銀の吸収除去にも効果的であると考えられ
、また、第1の実験により、チオ尿素・銅の共存する溶
液はガス状水銀除去に効果があると考えられる。
Therefore, considering the results of the first and second experiments together, it can be seen that in the second experiment, the mercury removal rate was about 90% or more,
The mercury concentration at the device outlet is 0. Since a treatment result of O8fEf/Nd or less was obtained, it is thought that a solution in which thiourea and copper coexist is effective in absorbing and removing gaseous mercury. A solution containing copper is considered to be effective in removing gaseous mercury.

なお、排ガスとしてゴミ焼却炉のものを例に挙げて説明
して来たが、産廃焼却炉の排ガスであっても同様の結果
が得られることは明らかである。
In addition, although the exhaust gas has been explained by taking as an example the exhaust gas from a garbage incinerator, it is clear that similar results can be obtained with the exhaust gas from an industrial waste incinerator.

すなわち、本発明方法は水銀含有排ガスの湿式洗煙設備
にひろく適用することが可能である。
That is, the method of the present invention can be widely applied to wet smoke cleaning equipment for mercury-containing exhaust gas.

発明の効果 以上本発明によれば、脱塩化水素(HCI)、脱硫黄酸
化物(SOx)と同時に排ガス中(ばいじん中子ガス中
)のガス状水銀を約90%以上除去できる。
Effects of the Invention According to the present invention, about 90% or more of gaseous mercury in the exhaust gas (in the dust core gas) can be removed at the same time as dehydrochlorination (HCI) and desulfurization oxides (SOx).

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

第1図は本発明方法を適用するための湿式洗煙設備フロ
ー図、第2図は第1の実験に用いたテスト装置のフロー
図、第8図は第2の実験に用いたテスト装置のフロー図
である。 (2)・・・チオ尿素、(3ン・・・塩化第1銅、(5
ン・・・苛性ソーダ、俵Q・・・焼却炉排ガス 代理人 森 本 義 弘
Figure 1 is a flow diagram of wet smoke cleaning equipment for applying the method of the present invention, Figure 2 is a flow diagram of the test equipment used in the first experiment, and Figure 8 is a flow diagram of the test equipment used in the second experiment. It is a flow diagram. (2)...thiourea, (3)...cuprous chloride, (5
N...Caustic soda, bales Q...Incinerator exhaust gas agent Yoshihiro Morimoto

Claims (1)

【特許請求の範囲】[Claims] 1、 チオ尿素と塩化第1銅を添加したアルカリ溶液で
排ガスを湿式洗煙することを特徴とする湿式洗煙設備で
のガス状水銀の除去方法。
1. A method for removing gaseous mercury using wet smoke scrubbing equipment, which is characterized by wet scrubbing exhaust gas with an alkaline solution containing thiourea and cuprous chloride.
JP58242531A 1983-12-21 1983-12-21 Removal of gaseous mercury in wet exhaust gas scrubbing equipment Pending JPS60132626A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58242531A JPS60132626A (en) 1983-12-21 1983-12-21 Removal of gaseous mercury in wet exhaust gas scrubbing equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58242531A JPS60132626A (en) 1983-12-21 1983-12-21 Removal of gaseous mercury in wet exhaust gas scrubbing equipment

Publications (1)

Publication Number Publication Date
JPS60132626A true JPS60132626A (en) 1985-07-15

Family

ID=17090495

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58242531A Pending JPS60132626A (en) 1983-12-21 1983-12-21 Removal of gaseous mercury in wet exhaust gas scrubbing equipment

Country Status (1)

Country Link
JP (1) JPS60132626A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6257631A (en) * 1985-09-04 1987-03-13 Hitachi Zosen Corp Method for reducing entrainment of mercury from circulating liquid cooling tower for dehumidifying waste gas
US4729882A (en) * 1985-03-28 1988-03-08 Tokyo Metropolitan Environmental Service Corporation Process for cleaning mercury-containing gaseous emissions
JPH10216476A (en) * 1997-01-31 1998-08-18 Kawasaki Heavy Ind Ltd Waste gas treatment and apparatus therefor
JP2015509845A (en) * 2012-03-15 2015-04-02 アルストム テクノロジー リミテッドALSTOM Technology Ltd Mercury capture system and method for wet flue gas desulfurization system

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4729882A (en) * 1985-03-28 1988-03-08 Tokyo Metropolitan Environmental Service Corporation Process for cleaning mercury-containing gaseous emissions
JPS6257631A (en) * 1985-09-04 1987-03-13 Hitachi Zosen Corp Method for reducing entrainment of mercury from circulating liquid cooling tower for dehumidifying waste gas
JPH054122B2 (en) * 1985-09-04 1993-01-19 Hitachi Shipbuilding Eng Co
JPH10216476A (en) * 1997-01-31 1998-08-18 Kawasaki Heavy Ind Ltd Waste gas treatment and apparatus therefor
JP2015509845A (en) * 2012-03-15 2015-04-02 アルストム テクノロジー リミテッドALSTOM Technology Ltd Mercury capture system and method for wet flue gas desulfurization system

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