JPS61278331A - Desulfurizing method for exhaust gas containing trace so2 - Google Patents
Desulfurizing method for exhaust gas containing trace so2Info
- Publication number
- JPS61278331A JPS61278331A JP60119820A JP11982085A JPS61278331A JP S61278331 A JPS61278331 A JP S61278331A JP 60119820 A JP60119820 A JP 60119820A JP 11982085 A JP11982085 A JP 11982085A JP S61278331 A JPS61278331 A JP S61278331A
- Authority
- JP
- Japan
- Prior art keywords
- exhaust gas
- liquid
- spray
- caustic soda
- concentration
- 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
Links
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、排ガス中にppmのオーダーの濃度で含まれ
ている亜硫酸ガス(SO2)を吸収、除去するための脱
硫方法に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a desulfurization method for absorbing and removing sulfur dioxide gas (SO2) contained in exhaust gas at a concentration on the order of ppm.
従】纂λ皮街πU肛
従来、湿式排煙脱硫法の多くはSO2の吸収帯域(吸収
塔、充テン層或はベンチュリーのスロート部等)を特別
に設けて、気−液接触により脱硫を行なっている。した
がって、従来法では上記吸収帯域としての設備も大型で
あって、そのだめのコストも可成り高くなることが避け
られない。Previously, in most wet flue gas desulfurization methods, a special SO2 absorption zone (absorption tower, packed layer, venturi throat, etc.) was provided, and desulfurization was carried out through gas-liquid contact. I am doing it. Therefore, in the conventional method, the equipment for the above-mentioned absorption band is large-sized, and the cost thereof is unavoidably high.
■が解ン しようとするPo 由
本発明者は、排ガスの脱硫を、特別な吸収帯域を設ける
必要がなく、簡易な手段で行ない得る方法について検討
した結果、502をppmのオーダーの程度の濃度で含
む排ガスでは、稀薄アルカリ液のスプレーと接触させる
と該排ガス中の302がアルカリ液に良く吸収され、且
つS02を吸収した液滴がガスと共に持ち去られないこ
とを見出し、本発明をなすに至った゛。The inventor of the present invention investigated a method for desulfurizing exhaust gas by a simple means without the need to provide a special absorption zone, and found that 502 was desulfurized at a concentration on the order of ppm. It was discovered that when the exhaust gas containing S02 is brought into contact with a spray of dilute alkaline liquid, the 302 in the exhaust gas is well absorbed by the alkaline liquid, and the droplets that have absorbed S02 are not carried away with the gas, leading to the present invention. .
したがって、本発明は502をppmのオーダーの濃度
で含む排ガスの脱硫を、特別な吸収帯域を用いることな
く、極めて簡易な手段で行ない得る方法を提供すること
を目的とする。Therefore, an object of the present invention is to provide a method that can desulfurize exhaust gas containing 502 at a concentration on the order of ppm by extremely simple means without using a special absorption zone.
以下本発明の詳細な説明する。The present invention will be explained in detail below.
光肌東橡戊
本発明の特徴は、亜硫酸ガスをppmのオーダーの濃度
で含む排ガス中に、稀薄なアルカリ液を噴霧状態で吹き
込むことにある。A feature of the present invention is that a dilute alkaline liquid is blown into the exhaust gas containing sulfur dioxide gas at a concentration on the order of ppm in the form of a spray.
上記排ガス中に稀薄なアルカリ液を噴霧状態で吹き込む
には、ジェット方式を適用してアルカリ液をスプレーし
、ノズルの周りから圧縮空気を入れて、この圧縮空気の
圧力とアルカリ液の流量を調節しながら行なう。この場
合、ガスの流れが乱流を起すように、好ましくは渦状の
乱流を起すようにノズルの取付位置及び空気の吹込み孔
を選択するようにする。To inject dilute alkaline liquid into the above exhaust gas in a spray state, apply the jet method to spray the alkaline liquid, then introduce compressed air from around the nozzle to adjust the pressure of this compressed air and the flow rate of the alkaline liquid. Do it while doing it. In this case, the mounting position of the nozzle and the air blowing hole are selected so that the gas flow is turbulent, preferably a swirling turbulence.
上述のようにして排ガス中にアルカリ液のスプレーを吹
き込むと、排ガスとアルカリ液のスプレーの混合、接触
が良くなって排ガス中のSO2はアルカリ液の比較的微
細な液滴に速やかに吸収される。When the alkaline liquid spray is injected into the exhaust gas as described above, the mixture and contact between the exhaust gas and the alkaline liquid spray improves, and the SO2 in the exhaust gas is quickly absorbed by the relatively fine droplets of the alkaline liquid. .
なお、アルカリ液の濃度と液温によってその噴霧状態が
若干変動するので、S02の吸収効果の高いスプレー条
件である10μ〜400μの液滴からなる噴霧が得られ
るように選定することが好ましい。In addition, since the spray condition varies slightly depending on the concentration and temperature of the alkaline liquid, it is preferable to select the spray condition so as to obtain a spray consisting of droplets of 10 μ to 400 μ, which is a spray condition that has a high absorption effect of S02.
ここで用いるアルカリ液としては、通常苛性ソーダ液が
適当であるが、排ガス中のSO2を吸収し得るものであ
ればよく、苛性カリ、水酸化カルシウム、水酸化マグネ
シウム等を例示し得る。As the alkaline liquid used here, a caustic soda solution is usually suitable, but any alkaline liquid that can absorb SO2 in the exhaust gas may be used, and examples thereof include caustic potash, calcium hydroxide, magnesium hydroxide, and the like.
また、アルカリ液の濃度と液温は約7%〜約15%程度
並びに約20℃程度が適当である。Further, the concentration and temperature of the alkaline solution are suitably about 7% to about 15% and about 20°C.
本発明によると、排ガスのガス道に上述のようにしてア
ルカリ液をスプレーで吹き込むだけの簡易な手段により
、排ガス中のSOxを低減させることが可能となる。According to the present invention, it is possible to reduce SOx in the exhaust gas by simply spraying the alkaline liquid into the exhaust gas path as described above.
の と9
以下に実施例を示して本発明とその効果をさらに具体的
に説明する。and 9 The present invention and its effects will be explained in more detail with reference to Examples below.
実施例1
502を100ppraの濃度で含む排ガス(ガス量7
3ONn?/min、ガス塩13℃)に、13%濃度の
苛性ソーダ水溶液(液温20°C)を70 N /hの
液量で、圧力3.0kg/cnlの圧縮空気を介してA
KI Jetを用いてスプレー状に吹き込んだ。なお、
スプレー位置でのガス流速ばl1m/secであった。Example 1 Exhaust gas containing 502 at a concentration of 100 ppra (gas amount 7
3ONn? A 13% concentration caustic soda aqueous solution (liquid temperature 20°C) was added at a flow rate of 70 N/h to a gas salt temperature of 13°C) via compressed air at a pressure of 3.0 kg/cnl.
It was injected into a spray using KI Jet. In addition,
The gas flow rate at the spray position was 11 m/sec.
排ガス中のSO2の除去率及び苛性ソーダの利用効率は
後記表1に示すとおりである。The removal rate of SO2 in the exhaust gas and the utilization efficiency of caustic soda are as shown in Table 1 below.
実施例2
排ガスとしてSO2を120ppmの濃度を含むものに
、15%濃度の苛性ソーダ水溶液(液温20°C)を8
0 I!/hの液量でスプレーする以外は、実施例Iと
同様にして脱硫を行なった。排ガス中の502の除去率
及び苛性ソーダの利用効率は後記表1に示すとおりであ
る。Example 2 A 15% concentration caustic soda aqueous solution (liquid temperature 20°C) was added to SO2 containing a concentration of 120 ppm as exhaust gas.
0 I! Desulfurization was carried out in the same manner as in Example I, except for spraying at a liquid volume of /h. The removal rate of 502 in the exhaust gas and the utilization efficiency of caustic soda are as shown in Table 1 below.
実施例3
13%濃度の苛性ソーダ水溶液を用いることに代えて7
%濃度の苛性ソーダ水溶液(液温20℃)を用い、かつ
30 Il/hの液量でスプレーする以外は、実施例1
と同様にして脱硫を行なった。排ガス中のSO2の除去
率及び苛性ソーダの利用効率は後記表1に示すとおりで
ある。Example 3 Instead of using a 13% aqueous caustic soda solution,
% concentration of caustic soda aqueous solution (liquid temperature 20°C) and spraying at a liquid volume of 30 Il/h.
Desulfurization was carried out in the same manner. The removal rate of SO2 in the exhaust gas and the utilization efficiency of caustic soda are as shown in Table 1 below.
実施例4
排ガスとしてSO2を120ppmの濃度で含むものに
、15%濃度の苛性ソーダ水溶液(液温20℃)を30
1 /hの液量でスプレーする以外は、実施例1と同様
にして脱硫を行なった。排ガス中の502の除去率及び
苛性ソーダの利用効率は後記表1に示すとおりである。Example 4 A 15% aqueous solution of caustic soda (liquid temperature 20°C) was added at 30°C to exhaust gas containing SO2 at a concentration of 120 ppm.
Desulfurization was carried out in the same manner as in Example 1, except that the solution was sprayed at a liquid volume of 1/h. The removal rate of 502 in the exhaust gas and the utilization efficiency of caustic soda are as shown in Table 1 below.
実施例5
本例は、苛性ソーダ水溶液の液温を15℃の低温でスプ
レーした場合を示したものであって、排ガスとして50
2を80ppmの濃度で含むものに、7%濃度の苛性ソ
ーダ水溶液(液温15°C)を601 /hのの液量で
スプレー以外は、実施例1と同様にして脱硫を行なった
。排ガス中のSO2の除去率及び苛性ソーダの利用効率
は表1に示すとおりである。Example 5 This example shows the case where a caustic soda aqueous solution is sprayed at a low temperature of 15°C, and the exhaust gas is 50°C.
Desulfurization was carried out in the same manner as in Example 1, except that a 7% concentration aqueous solution of caustic soda (liquid temperature 15°C) was sprayed at a volume of 601 /h onto a sample containing 80 ppm of 2. The removal rate of SO2 in the exhaust gas and the utilization efficiency of caustic soda are shown in Table 1.
表1にみられるとおり、苛性ソーダ水溶液の液温が15
℃と低くなると、SO2の毎時吸収量は別として、Na
OHの利用効率が低下するので、20℃程度の液温でス
プレーすることが好ましいことがわかる。As shown in Table 1, the temperature of the caustic soda aqueous solution is 15
At temperatures as low as ℃, apart from the hourly absorption of SO2, Na
It can be seen that it is preferable to spray at a liquid temperature of about 20° C. since the OH utilization efficiency decreases.
また、苛性ソーダ水溶液の濃度がlO〜15%程度、及
び液量が高い程S02の吸収量が向上することもわかる
。It can also be seen that the absorption amount of S02 improves as the concentration of the caustic soda aqueous solution increases from about 10 to 15% and as the amount of the solution increases.
Claims (3)
ス中に、稀薄なアルカリ液を噴霧状態で吹き込むことを
特徴とする上記排ガスのの脱硫方法。(1) The method for desulfurizing exhaust gas described above, which comprises blowing a dilute alkaline solution in a spray state into the exhaust gas containing sulfur dioxide gas at a concentration on the order of ppm.
溶液である特許請求の範囲第(1)項記載の脱硫方法。(2) The desulfurization method according to claim (1), wherein the alkaline liquid is an aqueous caustic soda solution having a concentration of about 7 to about 15%.
行なう特許請求の範囲第(1)項記載の脱硫方法。(3) The desulfurization method according to claim (1), wherein the alkaline liquid is atomized using compressed air.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60119820A JPS61278331A (en) | 1985-06-04 | 1985-06-04 | Desulfurizing method for exhaust gas containing trace so2 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60119820A JPS61278331A (en) | 1985-06-04 | 1985-06-04 | Desulfurizing method for exhaust gas containing trace so2 |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61278331A true JPS61278331A (en) | 1986-12-09 |
Family
ID=14771055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60119820A Pending JPS61278331A (en) | 1985-06-04 | 1985-06-04 | Desulfurizing method for exhaust gas containing trace so2 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61278331A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53119780A (en) * | 1977-11-21 | 1978-10-19 | Kureha Chem Ind Co Ltd | Treating method for exhaust gas |
-
1985
- 1985-06-04 JP JP60119820A patent/JPS61278331A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS53119780A (en) * | 1977-11-21 | 1978-10-19 | Kureha Chem Ind Co Ltd | Treating method for exhaust gas |
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