JPS5861822A - Deodorizing device for gas - Google Patents

Deodorizing device for gas

Info

Publication number
JPS5861822A
JPS5861822A JP56161381A JP16138181A JPS5861822A JP S5861822 A JPS5861822 A JP S5861822A JP 56161381 A JP56161381 A JP 56161381A JP 16138181 A JP16138181 A JP 16138181A JP S5861822 A JPS5861822 A JP S5861822A
Authority
JP
Japan
Prior art keywords
gas
ozone
tower
bromide
buffer
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
JP56161381A
Other languages
Japanese (ja)
Inventor
Takekuni Azuma
吾妻 健国
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 Electric Corp
Original Assignee
Mitsubishi Electric 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 Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP56161381A priority Critical patent/JPS5861822A/en
Publication of JPS5861822A publication Critical patent/JPS5861822A/en
Pending legal-status Critical Current

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  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
  • Treating Waste Gases (AREA)

Abstract

PURPOSE:To deodorizes gases to be treated efficiently by injection of ozone at a specified concn. by providing a buffer tower in the fore stage of a deodorozing tower which combines a deodorizer deposited with a bromine compd. and ozone thereby eliminating the fluctuations in the concn. of malodorous components. CONSTITUTION:Gases to be treated which have malodors are introduced into a buffer tower 7 like an arrow A, where the gases contact with the buffer agent 8 in the tower 7 and the concn. of the malodorous components is leveled off. Thereafter the ozone generated in an ozone generator 3 is injected into the gases through an ozone piping 6 like an arrow B, then the gases after the buffering contg. a prescribed concn. of ozone contact with a deodorizer 5 deposited with a bromine compd. in a deodorizing tower 4, whereby the gases are deodorized.

Description

【発明の詳細な説明】 この発明はオゾンによる気体の脱臭装胃に関し、さらに
評しくけ、臭素化合物を添着した活性炭等の悪臭物質の
吸着剤と化学的脱臭剤であるオゾンを組合せた高性能で
省エネルギ的な乾式の気体脱臭装置忙関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to gas deodorization using ozone, and has been further evaluated to achieve high performance by combining ozone, a chemical deodorizer, with an adsorbent for malodorous substances such as activated carbon impregnated with a bromine compound. This is an energy-saving dry type gas deodorizing device.

従来、この種の装置としては第1図に示すものがあった
。第1図は従来の気体脱臭装置を示すフロー図であり、
図において、(1)は急興を帯びた被処理気体をダクト
レ)に捕集するファン、(3)はオゾン発生器、(4)
は脱臭塔であり、その内部には臭素化合物を添着した脱
臭剤(5)が充填されている。(6)はオゾン配管であ
り、オゾン発生器(3)とダクト(2)を連結している
Conventionally, there has been a device of this type as shown in FIG. FIG. 1 is a flow diagram showing a conventional gas deodorizing device.
In the figure, (1) is a fan that collects rapidly increasing gas to be treated in a duct, (3) is an ozone generator, and (4)
is a deodorizing tower, the inside of which is filled with a deodorizing agent (5) impregnated with a bromine compound. (6) is an ozone pipe, which connects the ozone generator (3) and the duct (2).

久に動作について説明する。悪臭を帯びた被処理気体を
矢印Aのように、ファン+1)によってダク)(21に
導入した後、ファン(1−1の入口側で、オゾン発生!
 +31によって発生させたオゾンを、矢印Bのように
オゾン配管(6)を通して、被処理気体に所定濃度で混
入し、脱臭塔(4)に導く。脱臭塔(4)Kは臭素化合
物を添着した脱臭剤(5)が充填されており、被処理気
体は脱臭剤(5)と通常0.3〜1.5秒間接触する。
I will explain the operation shortly. After the foul-smelling gas to be treated is introduced into the duct) (21 by fan +1) as shown by arrow A, ozone is generated at the inlet side of fan (1-1).
The ozone generated by +31 is mixed into the gas to be treated at a predetermined concentration through the ozone pipe (6) as shown by arrow B, and is led to the deodorizing tower (4). The deodorizing tower (4) K is filled with a deodorizing agent (5) impregnated with a bromine compound, and the gas to be treated comes into contact with the deodorizing agent (5) for usually 0.3 to 1.5 seconds.

脱臭剤(5)として、例えば臭化水素(HBr)を活性
炭に添着させたものが充填されている場合。
When the deodorizer (5) is filled with, for example, activated carbon impregnated with hydrogen bromide (HBr).

脱臭剤(5)はその表面上で、被処理気体中のオゾンと
下記化学方程式(1)のように作用して臭素(Brl)
を生ずる。
On its surface, the deodorizer (5) acts with ozone in the gas to be treated as shown in the chemical equation (1) below to produce bromine (Brl).
will occur.

2HB r +03−+Br@ +H10+01   
   −(1)生成した臭素は脱臭剤(5)の表面にお
いて、被処理気体中の悪臭物質を酸化し、無臭の、tた
は著しく着臭の度合が低下した異種物質を生ずる0代表
的な悪臭成分に対する脱臭反応を例示すると、下記(2
)〜(4)式のようKなる。
2HB r +03-+Br@ +H10+01
- (1) The generated bromine oxidizes malodorous substances in the gas to be treated on the surface of the deodorizer (5), producing odorless or foreign substances with a significantly reduced degree of odor. To illustrate the deodorizing reaction against malodorous components, the following (2)
) to (4).

アンモニア 2NH3+ 3 B r2 →N2 + 6HB r 
      = (2)硫化水素 His +Brx→S+2HBr         =
 (3)または H雪S+3Brs+2HzO→80g+6HBr   
  −= (41化学方程式(2)〜K)において、臭
素は再び臭化水素にもどり、再度(1)式によるオゾン
酸化反応を受ける。
Ammonia 2NH3+ 3 B r2 →N2 + 6HB r
= (2) Hydrogen sulfide His +Brx→S+2HBr =
(3) or H Snow S+3Brs+2HzO→80g+6HBr
-= In (41 chemical equations (2) to K), bromine returns to hydrogen bromide and undergoes the ozone oxidation reaction according to equation (1) again.

上記従来の気体脱臭装置において、被処理気体に添加す
べきオゾンの量は少なくとも被処理気体中に含まれてい
る悪臭物質を酸化するのに必要な量が確保されねばなら
ないが、一般に、し尿処理場や下水処理場から発生する
着具した排気ガス中の悪臭ガス成分の種類や濃度は被処
理水の量や状態および水処理機器や汚泥処理設備の稼動
状態によって大幅に変化し、1日の間に3桁以上の濃度
範囲内で増減することもある。従って、必要オゾン量を
常時注入するKは、オゾン発生器が大規模なものkなシ
、設備費および電力消費量が増大して非経済的となるう
え、必要オゾン発生量の自動調節が技術的にも容易でな
いなどの欠点があった。
In the above-mentioned conventional gas deodorizing equipment, the amount of ozone to be added to the gas to be treated must be at least the amount necessary to oxidize the malodorous substances contained in the gas to be treated. The types and concentrations of malodorous gas components in exhaust gas generated from wastewater treatment plants and sewage treatment plants vary greatly depending on the amount and condition of water to be treated and the operating conditions of water treatment equipment and sludge treatment equipment. In some cases, the concentration may increase or decrease by more than three orders of magnitude over time. Therefore, constantly injecting the required amount of ozone requires a large-scale ozone generator, which increases equipment costs and power consumption, making it uneconomical. There were drawbacks such as the fact that it was not easy to do so.

この発明は上記のような従来の気体脱臭装置の欠点を除
去するため′になされたもので、従来の脱臭塔の前段に
緩衝基を設けることKよシ、急激な悪臭成分の濃度変動
をなくし、一定濃度のオゾン注入濃度で被処理気体を脱
臭することを可能にした気体脱臭装置を提供することを
目的としている。
This invention was made in order to eliminate the drawbacks of the conventional gas deodorizing equipment as described above, and instead of providing a buffer group at the front stage of the conventional deodorizing tower, it eliminates the rapid fluctuation in the concentration of malodorous components. The object of the present invention is to provide a gas deodorizing device that can deodorize a gas to be treated with a constant ozone injection concentration.

以下、この発明の一実施例を図について説明する。第2
図はこの発明の一実施例を示すフロー図であり1図にお
いて、第1図と同一符号は同一または相当部分を示す。
An embodiment of the present invention will be described below with reference to the drawings. Second
FIG. 1 is a flowchart showing an embodiment of the present invention. In FIG. 1, the same reference numerals as in FIG. 1 indicate the same or corresponding parts.

(7)は第1図に示す気体脱臭装置の前段に設けられた
緩衝基であ、?、(8)はその小に充填された緩衝剤で
ある。
(7) is a buffer group provided at the front stage of the gas deodorizing device shown in FIG. , (8) is the buffer filled in the container.

上記のように構成された気体脱臭装置において。In a gas deodorizing device configured as described above.

悪臭を帯びた被処理気体は矢印Aのように緩衝基(7)
に導入され、緩衝基(7)内の緩衝剤(8)と接触して
悪臭成分濃度が平滑化され、その後オゾン発生器(3)
において発生したオゾンが矢印Bのようにオゾン配管(
6)から注入され、第1図の場合と同様に脱臭塔(4)
において、臭素化合物全添着した脱臭剤(団と接触し、
脱臭される。
The foul-smelling gas to be treated is buffered as shown by arrow A (7).
The ozone generator (3)
The ozone generated in the ozone pipe (
6), and the deodorizing tower (4) is injected as in the case of Fig. 1.
In the process, the deodorizer with all the bromine compounds attached (contacts with the group,
Deodorized.

緩衝剤の)としては、被処理気体中の大幅なlI!度変
動を起こしている主要悪臭成分に対する吸着能 □力が
大きく、かつ複数の愚息成分に対して有効な吸着能力を
もつものが好ましい。例えば、最も濃度変動の激しい硫
化水素を対象にする場合、緩衝剤としては市販の木質系
1石炭質もしくはヤシ殻質等の各種の活性炭、または硫
化水素と化学反応を起こす水酸化ナトリウム、ヨウ化ナ
トリウム、ヨウ化カリウム等の薬品を上記活性炭または
活性アルミナ、合成ゼオライト、活性白土等の多孔質担
体に含浸させたものが使用できる。
) of the buffering agent, there is a significant lI! in the gas to be treated! Adsorption ability for major malodorous components that cause temperature fluctuations □It is preferable to use a material that has a large strength and has an effective adsorption ability for multiple bad odor components. For example, when dealing with hydrogen sulfide, which has the most severe concentration fluctuations, the buffering agent may be various types of activated carbon such as commercially available wood-based coal or coconut shell, or sodium hydroxide or iodide, which chemically reacts with hydrogen sulfide. Porous carriers such as the above activated carbon, activated alumina, synthetic zeolite, activated clay, etc., impregnated with chemicals such as sodium and potassium iodide can be used.

硫化水素とともにメチルメルカプタンをも同時に処理す
る必要がちも場合には、緩衝剤としては上記薬品を添着
しない活性炭、またはヨウ化物を含浸させた多孔質吸着
剤を使用することができる。
If it is necessary to treat hydrogen sulfide and methyl mercaptan at the same time, activated carbon not impregnated with the above-mentioned chemicals or a porous adsorbent impregnated with iodide can be used as the buffer.

またアンモニア、トリメチルアミン等の塩基性悪臭物質
を対象とする場合には、#A酸、硫酸等の鉱酸の水溶液
を含浸させた多孔質吸着剤を用いればよい。さらに硫化
水素と一アンモニアの両方を処理し丸い場合には、硫化
水素用およびアンモニア用の2種類の緩衝剤を被処理気
体の流れる方向に直列に配列するか、tIA化第1鉄、
*化第2鉄等の水に溶けて酸性を呈する重金属塩を含浸
させた多孔質吸着剤を用いる。
Furthermore, when the target is a basic malodorous substance such as ammonia or trimethylamine, a porous adsorbent impregnated with an aqueous solution of a mineral acid such as #A acid or sulfuric acid may be used. Furthermore, if both hydrogen sulfide and monoammonia are treated and round, two types of buffers for hydrogen sulfide and ammonia are arranged in series in the flow direction of the gas to be treated, or tIA ferrous,
*A porous adsorbent impregnated with a heavy metal salt that dissolves in water and exhibits acidity, such as ferric oxide, is used.

次K、緩衝剤の悪臭成分濃度の平滑能力について説明す
る。被処理気体中の成る悪臭成分の分圧がp*tmのと
き、緩衝剤1kgが吸着できる悪臭成分の量をω〜とす
ると、ωとpとの間には経験的に(5)式の関係が成り
立つ。
Next, the ability of the buffer to smooth the concentration of malodorous components will be explained. When the partial pressure of the malodorous components in the gas to be treated is p*tm, and the amount of malodorous components that can be adsorbed by 1 kg of buffer is ω~, then empirically, the relationship between ω and p is expressed by equation (5). A relationship is established.

ω= *p−(5) ここで、a、bは吸着剤、対象悪臭成分、吸着剤温度等
によって決められる定数である。
ω= *p-(5) Here, a and b are constants determined by the adsorbent, the target malodor component, the adsorbent temperature, etc.

悪臭成分が硫化水素、吸着剤が水酸化す) IJウムを
添着した活性炭の場合の例として、(5式は次のように
なる。
The malodorous component is hydrogen sulfide, and the adsorbent is hydroxide.) As an example of activated carbon impregnated with IJium, (Equation 5 is as follows.

ω= 2.30 po・”   (20℃)・・・帖)
(6)式において、緩衝剤が長時間被処理気体と接触し
、25チ(ω=0.25)の硫化水素を吸着したとする
と、そのときの緩衝剤のもつ平衡硫化水素背圧ゆ)は2
.14 X 10  atm である。従って、被処理
気体中の硫化水素濃度が2.14 X 10  atm
以上になると、緩衝剤(8)による種化水素の吸着能力
が生じて、被処理気体中の硫化水素が緩衝剤6)硫化水
素濃度は緩衝塔(7)に入るそれよりも減少し2.14
X10  atmlc近い濃度になる。一方、緩衝塔(
7)に入る被処理気体中の硫化水素#1度が2.14X
 10””ata+  (平衡背圧)以下になると、緩
衝剤β)の硫化水素吸着能力は消失し逆に緩衝剤(8)
から硫化水素が脱着されて、脱臭塔(4)に導入される
硫化水素のil[は増大して2.14 X 10−’a
tmに近づく。悪臭成分がメチルメルカプタンやアンモ
ニアであっても緩衝剤を適切に選定することによって上
述の硫化水素濃度のa衝と同じ効果を挙げることができ
る。
ω = 2.30 po・” (20℃)...Chapter)
In equation (6), if the buffer is in contact with the gas to be treated for a long time and adsorbs 25 cm (ω = 0.25) of hydrogen sulfide, then the equilibrium hydrogen sulfide back pressure of the buffer is is 2
.. 14×10 atm. Therefore, the hydrogen sulfide concentration in the gas to be treated is 2.14 x 10 atm
At this point, the adsorption capacity of the seeded hydrogen by the buffer (8) is generated, and the concentration of hydrogen sulfide in the gas to be treated decreases compared to that entering the buffer tower (7). 14
The concentration will be close to X10 atmlc. On the other hand, the buffer tower (
7) Hydrogen sulfide #1 degree in the gas to be treated entering is 2.14X
When it becomes less than 10"" ata+ (equilibrium back pressure), the hydrogen sulfide adsorption ability of buffer (β) disappears, and conversely, the hydrogen sulfide adsorption ability of buffer (8) disappears.
Hydrogen sulfide is desorbed from the hydrogen sulfide and introduced into the deodorizing tower (4).
Approaching tm. Even if the malodorous component is methyl mercaptan or ammonia, by appropriately selecting a buffering agent, the same effect as the above-mentioned a-buffering of hydrogen sulfide concentration can be achieved.

緩衝剤(8)の充填量は緩衝剤の対象悪臭成分の吸焉容
蓋によって異なるが、効果的な吸・脱着作用が起ζるた
めには1通常1秒以上の被処理気体との接触時間が保た
れるような充填量とする。硫化水素−変を平滑化させる
場合、緩衝剤(8)として用いる水酸化ナトリウムまた
はヨウ化カリウム添着活性炭の充填比重を500#/m
’、被処理気体との接触時間を1秒とし、(6)式にお
けるω=0.25に9(Hz S )/kfi (緩衝
剤とすると、被処理気体中の硫化水素濃度が10 X 
10−’ atm K上昇したとき。
The filling amount of the buffering agent (8) varies depending on the absorption capacity of the target malodorous component, but in order for effective adsorption and desorption to occur, contact with the gas to be treated for 1 second or more is usually required. The amount of filling should be such that the time is maintained. When smoothing hydrogen sulfide, the filling specific gravity of activated carbon impregnated with sodium hydroxide or potassium iodide used as a buffer (8) is 500#/m.
', the contact time with the gas to be treated is 1 second, and ω = 0.25 in equation (6) is 9 (Hz S )/kfi (if the buffer is used, the hydrogen sulfide concentration in the gas to be treated is 10
10-' atm K rises.

緩衝剤は2.14 X 10  aimを超える硫化水
素を吸着し、その能力はω= 0.32に達するまで持
続する。その緩衝作用の持続時間T、は、被処理気体量
をI N −/ ssjとして。
The buffer adsorbs more than 2.14 X 10 aim of hydrogen sulfide and its ability lasts until reaching ω = 0.32. The duration T of the buffering effect is given by the amount of gas to be treated as I N −/ssj.

3.600X1/22.4XΔpX34XTs =50
0X(0,32〒0.25)ΔFく(10−2,14)
XIO−’ ・°・Tt 〉815 I(r 、すなわち815時間
以上になる。
3.600X1/22.4XΔpX34XTs =50
0X(0,32〒0.25)ΔF(10-2,14)
XIO-' ・°・Tt 〉815 I(r, that is, more than 815 hours.

−万、硫化水素濃度が0.5 X 10−’ atmに
減少したとき、ω=0.195 (jl=o、5 X 
10−’atmに対応する値)Kなるまで、*衝剤の)
から硫化水素が脱着し続け、その持続時間T、は。
-10,000, when the hydrogen sulfide concentration decreases to 0.5 X 10-' atm, ω=0.195 (jl=o, 5
10 - the value corresponding to 'atm) until K, *of the shock agent)
Hydrogen sulfide continues to be desorbed from T, for a period of time T.

3600X1/22.4X(2,14−0,5)XIO
X34XT*〉500(0,25−0,195) ”Ts>3070Hr、すなわち3070時間以上に&
る。
3600X1/22.4X(2,14-0,5)XIO
X34XT*>500 (0,25-0,195) ”Ts>3070Hr, that is, over 3070 hours &
Ru.

上記緩衝作用の持続時間の推算値に対して、し尿処理場
や下水処理場から発生する着果した排ガスに含まれる悪
臭成分の濃度は1日24時間の周期で変動するので、上
記緩衝剤の緩衝作用の持続時間は必要量の3〜4倍以上
も長い。従って充分な緩衝作用を発揮する。
Regarding the estimated duration of the buffering effect mentioned above, since the concentration of malodorous components contained in the final waste gas generated from human waste treatment plants and sewage treatment plants fluctuates every 24 hours a day, The duration of the buffering action is 3 to 4 times longer than the required amount. Therefore, it exhibits a sufficient buffering effect.

なお、上記実施例においてはファン(1)の#に緩衝塔
(7)を設けたが、ファン(1)を緩衝塔(7)の前に
配置してもよい。また脱臭塔A)に充填される脱臭剤(
5)K添着する臭素化合物としては、臭化水素、tたは
臭化ナトリウム、臭化カリウム、臭化リチウム等のアル
カリ金属の臭化物、あるいは臭化マグネシウム、臭化カ
ルシウム勢のアルカリ土類金属の臭化物のうちの1種類
以上の水溶性物質を使用することができる。
In the above embodiment, the buffer tower (7) is provided at # of the fan (1), but the fan (1) may be placed in front of the buffer tower (7). Also, the deodorizing agent (
5) Bromine compounds to be impregnated with K include hydrogen bromide, alkali metal bromides such as sodium bromide, potassium bromide, and lithium bromide, or alkaline earth metal bromides such as magnesium bromide and calcium bromide. One or more water-soluble substances of bromides can be used.

本発明の気体脱臭装置はし尿処理場および下水処理場か
ら発生する悪臭ガスその他の着臭ガスの脱臭装置に適用
可能である。
The gas deodorizing device of the present invention is applicable to deodorizing devices for malodorous gas and other odorous gases generated from human waste treatment plants and sewage treatment plants.

以上のとおり1本発明によれば、被処理気体の悪臭成分
濃度の緩l1iSFrを設けたので、被処理気体を緩衝
塔(7)K通すととくよって、被処理気体中の悪臭成分
の濃度は平滑化されて、脱臭塔(4)K導入される。こ
のため、被処理気体中の悪臭成分の濃度に同期させてオ
ゾン濃度を変えること屯、大過剰のオゾンを添加する必
要もなく、オゾン発生器(3)は1日の平均的なオゾン
必要量を供給すればよい。従って、オゾン発生器(3)
が小形になるうえ。
As described above, according to the present invention, the concentration of malodorous components in the gas to be treated is moderated by SFr, so when the gas to be treated is passed through the buffer tower (7) K, the concentration of malodorous components in the gas to be treated is reduced. It is smoothed and introduced into the deodorizing tower (4)K. Therefore, there is no need to change the ozone concentration in synchronization with the concentration of malodorous components in the gas to be treated, and there is no need to add a large excess of ozone. All you have to do is supply it. Therefore, the ozone generator (3)
Not only does it become smaller, but it also becomes smaller.

脱臭装置全体が省エネルギ化されるなどの効果がある。This has the effect of saving energy for the entire deodorizing device.

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

第1図は従来のオゾンと臭素化合物添着訳を併用した乾
式脱臭装置を示すフロー図、第2図はこの発明の一実施
例の気体脱臭装置を示すフロー図である。 図中、(1)はファン、(3)はオゾン発生器、(4)
は脱臭塔、(5)は脱臭剤、(7)は緩衝基、侶)は緩
衝剤である。 なお、図中、同一符号は同一または相当部分を示す。 代理人  葛 野 信 −(外1名)
FIG. 1 is a flowchart showing a conventional dry deodorizing device using both ozone and bromine compound impregnation, and FIG. 2 is a flowchart showing a gas deodorizing device according to an embodiment of the present invention. In the diagram, (1) is a fan, (3) is an ozone generator, and (4)
is a deodorizing tower, (5) is a deodorizing agent, (7) is a buffer group, and (2) is a buffering agent. In addition, in the figures, the same reference numerals indicate the same or corresponding parts. Agent Shin Kuzuno - (1 other person)

Claims (1)

【特許請求の範囲】 (1)着臭した気体中の悪臭成分を一時的に吸″着除去
するか、除去した悪臭成分を再放出することによって着
臭した気体中の悪臭成分の製置をpImする緩衝塔、こ
の緩衝塔を通過した気体にオゾンを混合する手段および
臭素化合物を添着した脱臭剤が充填され、かつ上記オゾ
ンを混合した気体と接触するように配置された脱臭塔を
備えたことを特徴とする気体脱臭装置。 C)緩衝塔は活性炭または水酸化ナトリウム、#A酸、
ヨウ化カリウムもしくはヨウ化ナトリウムを多孔質担体
に含浸させた吸着剤を充填したものであることを特徴と
する特許請求の範囲第1項記載の気体脱臭装置。 (3)臭素化合物は臭化水素、臭化ナトリウム、臭化カ
リウム、臭化リチウム、臭化マグネシウム。 および臭化カルシウムのうちのlfi類以上の水溶性物
質であることを特徴とする特許請求の範囲第1項または
第2項記載の気体脱臭装置。
[Scope of Claims] (1) The production of malodorous components in odorous gas by temporarily adsorbing and removing the malodorous components in odorous gas or re-releasing the removed malodorous components. A buffer tower for pIm, a means for mixing ozone into the gas that has passed through the buffer tower, and a deodorizing tower filled with a deodorizer impregnated with a bromine compound and arranged so as to be in contact with the gas mixed with the ozone. A gas deodorizing device characterized by: C) The buffer tower contains activated carbon or sodium hydroxide, #A acid,
The gas deodorizing device according to claim 1, characterized in that the device is filled with an adsorbent in which a porous carrier is impregnated with potassium iodide or sodium iodide. (3) Bromine compounds include hydrogen bromide, sodium bromide, potassium bromide, lithium bromide, and magnesium bromide. The gas deodorizing device according to claim 1 or 2, wherein the gas deodorizing device is a water-soluble substance of lfi or higher class among calcium bromide and calcium bromide.
JP56161381A 1981-10-09 1981-10-09 Deodorizing device for gas Pending JPS5861822A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56161381A JPS5861822A (en) 1981-10-09 1981-10-09 Deodorizing device for gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56161381A JPS5861822A (en) 1981-10-09 1981-10-09 Deodorizing device for gas

Publications (1)

Publication Number Publication Date
JPS5861822A true JPS5861822A (en) 1983-04-13

Family

ID=15734002

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56161381A Pending JPS5861822A (en) 1981-10-09 1981-10-09 Deodorizing device for gas

Country Status (1)

Country Link
JP (1) JPS5861822A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005305218A (en) * 2004-04-16 2005-11-04 Osaka Gas Co Ltd Method and apparatus for leveling gas component concentration and gas component treatment apparatus
JP2013198845A (en) * 2012-03-23 2013-10-03 Kyuchaku Gijutsu Kogyo Kk Smoothing method of easily-adsorbable component concentration and apparatus

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005305218A (en) * 2004-04-16 2005-11-04 Osaka Gas Co Ltd Method and apparatus for leveling gas component concentration and gas component treatment apparatus
JP2013198845A (en) * 2012-03-23 2013-10-03 Kyuchaku Gijutsu Kogyo Kk Smoothing method of easily-adsorbable component concentration and apparatus

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