JPS5933011B2 - Ozone deodorization equipment - Google Patents

Ozone deodorization equipment

Info

Publication number
JPS5933011B2
JPS5933011B2 JP54001283A JP128379A JPS5933011B2 JP S5933011 B2 JPS5933011 B2 JP S5933011B2 JP 54001283 A JP54001283 A JP 54001283A JP 128379 A JP128379 A JP 128379A JP S5933011 B2 JPS5933011 B2 JP S5933011B2
Authority
JP
Japan
Prior art keywords
gas
container
ozone
aqueous solution
spray
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
Application number
JP54001283A
Other languages
Japanese (ja)
Other versions
JPS5594622A (en
Inventor
信好 海賀
敏昭 関
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.)
Toshiba Corp
Original Assignee
Tokyo Shibaura Electric Co 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 Tokyo Shibaura Electric Co Ltd filed Critical Tokyo Shibaura Electric Co Ltd
Priority to JP54001283A priority Critical patent/JPS5933011B2/en
Publication of JPS5594622A publication Critical patent/JPS5594622A/en
Publication of JPS5933011B2 publication Critical patent/JPS5933011B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明はオゾン脱臭装置の改良に関するものである。[Detailed description of the invention] The present invention relates to an improvement in an ozone deodorizing device.

従来下水処理場、し尿処理場などにおいて、アンモニア
、メチルメルカプタン、硫化水素、硫化メチル、トルメ
チルアミンその他不快な臭気を有する物質が大気中に放
散され、その濃度が高い場合には生活環境を悪化するの
で、悪臭防止法等によってその排出限度が規制されてい
る。
Conventionally, in sewage treatment plants, human waste treatment plants, etc., ammonia, methyl mercaptan, hydrogen sulfide, methyl sulfide, tolumethylamine, and other substances with unpleasant odors are released into the atmosphere, and when their concentrations are high, they worsen the living environment. Therefore, the emission limit is regulated by the Offensive Odor Prevention Act.

それら悪臭物質の脱臭除去する方法には、吸着剤で吸着
除去する方法、薬液で洗浄する方法、オゾン酸化と水洗
、オゾン酸化と薬液洗浄、水洗と触媒−酸化の組み合せ
による方法等が採用されている。
Methods used to deodorize and remove these malodorous substances include adsorption removal with an adsorbent, cleaning with a chemical solution, ozone oxidation and water washing, ozone oxidation and chemical washing, and a combination of water washing and catalyst-oxidation. There is.

代表的な悪臭物質とオゾンとの反応は次の化学式で示さ
れる。
The reaction between a typical malodorous substance and ozone is shown by the following chemical formula.

硫化水素 メチルメルカプタン 硫化メチル トリメチルアミン このように悪臭物質は、オゾン酸化を受は無臭の化合物
もしくは臭気の弱い物質に変化するとともに、水に対す
る溶解性が太き(なり、水洗とオゾン酸化を併用するこ
とによってかなりの除去効果を期待することができる。
Hydrogen sulfide Methyl mercaptan Sulfide Methyl trimethylamine In this way, malodorous substances undergo ozone oxidation and change into odorless compounds or substances with a weak odor, and their solubility in water increases (so that washing with water and ozone oxidation must be used together). A considerable removal effect can be expected.

特に硫化物系の悪臭物質濃度が高い場合には、水洗とオ
ゾン酸化よりアルカリ洗浄とオゾン酸化を併用した方が
効果が太き(、更には粉末活性炭をスラリ状で共存させ
ると比較的弱いアルカリ性(PH8〜9)でも、硫化水
素除去率60〜90%が得られることが判かった。
In particular, when the concentration of sulfide-based malodorous substances is high, it is more effective to use alkaline cleaning and ozone oxidation together than to wash with water and ozone oxidation (furthermore, if powdered activated carbon coexists in the form of a slurry, it will give a relatively weak alkaline effect. It was found that a hydrogen sulfide removal rate of 60 to 90% could be obtained even when the pH was 8 to 9.

これは、アルカリと反応した後オゾンと反応する下記の
化学式以外に 2NaOH+H2S−+Na2S+2H2ONa S十
H2S−→2NaH8 Na S十03→Na2SO3 NaH8+0 →NaH803 h Na2SO3+03−>Na2SO4+02N
aH8O3+03→NaH8O4+02活性炭の固体触
媒作用により、吸収液に溶解後学気中酸素によって次の
ように順次酸化されるため、弱アルカリ性溶液でも比較
的高い除去率が得られたものと考えられる。
In addition to the chemical formula below that reacts with alkali and then reacts with ozone, 2NaOH + H2S- + Na2S + 2H2ONa S + H2S- → 2NaH8 Na S +03 → Na2SO3 NaH8+0 → NaH803 h Na2SO3+03->Na2SO4+02N
aH8O3+03→NaH8O4+02 Due to the solid catalytic action of the activated carbon, after being dissolved in the absorption liquid, it is oxidized by atmospheric oxygen in the following order, which is why a relatively high removal rate was obtained even with a weakly alkaline solution.

この弱アルカリ性で硫化水素系悪臭成分が吸収除去でき
ると言うことは、下水処理場、し尿処理場などの好気性
微生物処理を行なった炭酸ガスを多く含む排ガスの脱臭
には、アルカリ消費量が少なくてよく、更にオゾンと殆
ど反応しないで多量に検出されるアンモニアの水洗効果
も生じるため、酸性ガス、アルカリ性ガスの共存するも
のには大きな効果を示す。
The fact that this weak alkalinity can absorb and remove hydrogen sulfide-based malodorous components means that the amount of alkali consumed is small and can be used to deodorize exhaust gas containing a lot of carbon dioxide gas that has been treated with aerobic microorganisms at sewage treatment plants, human waste treatment plants, etc. In addition, since ammonia, which hardly reacts with ozone and is detected in large quantities, has a washing effect with water, it has a great effect when acidic gases and alkaline gases coexist.

しかし弱アルカリ水溶液の活性炭スラリをスプレなどで
吸収塔に散布する運転では、活性炭の吸収塔充填材に対
する不均一な付着もしくは沈降分離、パイプ目づまり等
を発生する不都合があった。
However, in an operation in which activated carbon slurry containing a weak alkaline aqueous solution is applied to the absorption tower by spraying or the like, there are disadvantages such as uneven adhesion or sedimentation of the activated carbon to the absorption tower filling material, clogging of pipes, etc.

本発明は上記の欠点を解消するためになされたもので、
吸収塔充填材に石炭や木炭等のような炭素質材料を用い
、弱アルカリ水溶液でオゾンを添加した被処理気体を洗
浄し、脱臭するオゾン脱臭装置を提供することを目的と
するものである。
The present invention has been made to solve the above-mentioned drawbacks.
The object of the present invention is to provide an ozone deodorizing device that uses a carbonaceous material such as coal or charcoal as an absorption tower filler, and cleans and deodorizes a gas to be treated to which ozone has been added with a weak alkaline aqueous solution.

以下本発明の一実施例を図面に基づいて説明する。An embodiment of the present invention will be described below based on the drawings.

第゛1図において、悪臭を有する被処理気体(以下単に
被処理気体という)は、プロワ1およびオゾン発生器2
を有する被処理気体供給装置にて、まずブロワ1により
吸引されオゾン発生器2で生成されたオゾン化ガスを添
加混合された後、洗浄塔3用の容器の下部空間内に送ら
れる。
In FIG.
In the treatment gas supply device having a gas to be treated gas, first, the ozonized gas sucked by the blower 1 and generated by the ozone generator 2 is added and mixed, and then sent into the lower space of the container for the cleaning tower 3.

ここで下水し尿処理場で排気中のオゾンと反応性の高い
トリメチルアミン、メルカプタン類は一部気相酸化され
るが、比較的高濃度で検出される硫化水素は、殆ど気相
酸化されず未反応オゾンと共に洗浄塔3を上昇する。
Trimethylamine and mercaptans, which are highly reactive with ozone in the exhaust gas at sewage and human waste treatment plants, are partially oxidized in the gas phase, but hydrogen sulfide, which is detected at relatively high concentrations, is hardly oxidized in the gas phase and remains unreacted. It ascends the cleaning tower 3 together with ozone.

この洗浄塔3内の中間部には、気液接触効率を大きくす
るためと固体触媒となる炭素質材料4が保持棚5上に充
填材として収容されており、被処理気体が上昇する際、
スプレ6から連続的に散布される弱アルカリ性水溶液に
硫化物イオンとして吸収され、炭素質材料4表面の触媒
作用を受け、未反応オゾンだけでな(空気中酸素によっ
ても亜硫酸イオン、硫酸イオン等に酸化される。
A carbonaceous material 4 serving as a solid catalyst is housed in the intermediate part of the cleaning tower 3 on a holding shelf 5 as a filler in order to increase the gas-liquid contact efficiency, and when the gas to be treated rises,
It is absorbed as sulfide ions in the weakly alkaline aqueous solution continuously sprayed from the spray 6, and is catalyzed by the surface of the carbonaceous material 4. Oxidized.

この酸化によって溶液PHは低下し、アミン、アンモニ
アの悪臭成分をも吸収除去する。
This oxidation lowers the pH of the solution and also absorbs and removes malodorous components such as amines and ammonia.

本発明における炭素質材料とは、石炭、木炭等のような
天然炭素質材であり、空隙率の高いコークスでもよいが
多孔質の木材構造をそのまま保有している亜炭、褐炭更
には黒炭、白炭等の木炭の方がよい。
The carbonaceous material in the present invention is a natural carbonaceous material such as coal, charcoal, etc., and may be coke with a high porosity, but also lignite, brown coal, black coal, white coal, etc., which retain the porous wood structure. charcoal is better.

これらは活性炭の比表面積15000〜2000m’/
グに比較して、亜炭、褐炭で250〜40077+3/
グ、黒炭で350〜400 m/?、白炭で200〜2
50m’/グと低いが、一定の固まりとして充填すれば
適当な空隙が形成できるので、気液接触効率を向上させ
るための、充填材と利用できる。
These have a specific surface area of activated carbon of 15,000 to 2,000 m'/
250~40077+3/ for lignite and brown coal
350-400 m/? ,200~2 with white charcoal
Although it is as low as 50 m'/g, if it is filled in a certain mass, appropriate voids can be formed, so it can be used as a filler to improve the gas-liquid contact efficiency.

又炭素質材料表面では、気体との反応ではなく洗浄液を
通しての溶液と固体の反応であるため、黒炭では水分を
多く吸収する松、カエデ等よりも辺材部を残し心材部に
放射状の割れが入って空隙の大きいクヌギ、ナラ、クリ
等の方が、送風に対する抵抗の減少と洗浄液の移動や流
通には都合がよくなる。
In addition, on the surface of carbonaceous materials, the reaction is not with gas but with the solution passing through the cleaning liquid and solid, so black charcoal leaves the sapwood and causes radial cracks in the heartwood compared to pine, maple, etc., which absorb a lot of water. Sawtooth oak, oak, chestnut, etc., which have large pores, reduce resistance to air blowing and are more convenient for the movement and distribution of the cleaning solution.

しかして処理された被処理気体は、デミスタ7でミスト
の除去が行なわれ大気中へ放出される。
The treated gas is subjected to mist removal in a demister 7 and is released into the atmosphere.

一方洗浄塔3用の容器に設けた下部排水口から流下した
洗浄液は、沈殿槽8に入り、細かくなり排出された炭素
質材料を沈殿後調整槽9に入る。
On the other hand, the cleaning liquid flowing down from the lower drainage port provided in the container for the cleaning tower 3 enters the sedimentation tank 8, and the finely discharged carbonaceous material is precipitated and then enters the adjustment tank 9.

この調整槽9は後述するポンプ10と共に弱アルカリ水
溶液供給装置を構成する。
This adjustment tank 9 constitutes a weak alkaline aqueous solution supply device together with a pump 10 which will be described later.

ポンプ10は調整槽9内の弱アルカリ水溶液を吸引し、
再びスプレ6から散布させる。
The pump 10 sucks the weak alkaline aqueous solution in the adjustment tank 9,
Spray again from spray 6.

すなわち、弱アルカリ水溶液供給装置は、被処理気体が
洗浄塔3に供給されている間は連続的に動作し、スプレ
6を介して洗浄塔3内に弱アルカリ水溶液を供給し続け
る。
That is, the weak alkaline aqueous solution supply device operates continuously while the gas to be treated is being supplied to the cleaning tower 3, and continues to supply the weak alkaline aqueous solution into the cleaning tower 3 via the spray 6.

ここで調整槽9では、PH計11によりPHが測定され
所定のPHより低下した場合にアルカリ貯留槽12から
苛性ソーダもしくは炭酸ソーダ等の濃厚溶液が自動的に
加えられ、一定のPHに保たれる。
Here, in the adjustment tank 9, the pH is measured by a pH meter 11, and when the pH drops below a predetermined value, a concentrated solution such as caustic soda or soda carbonate is automatically added from the alkaline storage tank 12 to maintain a constant pH. .

又洗浄液の一部は、オーバーフロ管13から一定量排出
され、この排出水量と水分蒸発分を補なうために補給水
管14から水が補給される。
Further, a certain amount of the cleaning liquid is discharged from the overflow pipe 13, and water is replenished from the replenishment water pipe 14 to compensate for the amount of discharged water and the evaporated water.

なお同図中15はPH調整装置、16はアルカリ貯留槽
12からアルカリ溶液を調整槽9に補給するバルブであ
り、又保持棚5は第2図に示すように複数用いて高い空
隙率を保有させるようにしてもよく、更に第3図に示す
ように複数設けた保持棚5上の炭素質材料4ごとにスプ
レ6から洗浄液を散布するようにしてもよい。
In the same figure, 15 is a pH adjustment device, 16 is a valve for replenishing alkaline solution from the alkaline storage tank 12 to the adjustment tank 9, and a plurality of holding shelves 5 are used as shown in FIG. 2 to maintain a high porosity. Furthermore, as shown in FIG. 3, the cleaning liquid may be sprayed from the spray 6 onto each carbonaceous material 4 on a plurality of holding shelves 5.

以上説明したように本発明によれば、活性炭と同様な固
体触媒を充填材として用いるために、従来のように粉末
活性炭を用い懸濁による目づまり、沈降分離、配管破損
等がなくなり安定した運転を確保することができる。
As explained above, according to the present invention, since a solid catalyst similar to activated carbon is used as a filler, there is no clogging due to suspension, sedimentation separation, piping damage, etc. using powdered activated carbon as in the past, resulting in stable operation. can be ensured.

【図面の簡単な説明】 第1図は本発明の一実施例の概略を示す構成図、第2図
は本発明の他の実施例の要部を示す構成図、第3図は本
発明の更に異なる他の実施例の要部を示す構成図である
。 3・・・・・・容器、4・・・・・・炭素質材料、6・
・・・・・スプレ、8・・・・・・沈殿槽。
[BRIEF DESCRIPTION OF THE DRAWINGS] Fig. 1 is a block diagram showing an outline of one embodiment of the present invention, Fig. 2 is a block diagram showing main parts of another embodiment of the present invention, and Fig. 3 is a block diagram showing an outline of an embodiment of the present invention. It is a block diagram which shows the principal part of yet another different Example. 3... Container, 4... Carbonaceous material, 6.
...Spray, 8... Sedimentation tank.

Claims (1)

【特許請求の範囲】[Claims] 1 下部排水口を有し上部にスプレーを設けた容器と、
この容器内の中間部に収容された固体状を成す炭素質材
料と、上記容器の下部空間内にオゾン化気体が混合され
た被処理気体を供給する被処理気体供給装置と、この被
処理気体供給装置により前記容器に被処理気体が供給さ
れている間前記スプレーを介して容器内に弱アルカリ水
溶液を供給する弱アルカリ水溶液供給装置とを備えたオ
ゾン脱臭装置。
1. A container with a bottom drain and a spray on the top,
A solid carbonaceous material housed in an intermediate portion of the container; a gas supply device for supplying a gas to be treated mixed with ozonized gas into a lower space of the container; An ozone deodorizing device comprising: a weak alkaline aqueous solution supply device that supplies a weak alkaline aqueous solution into the container through the spray while the gas to be treated is supplied to the container by the supply device.
JP54001283A 1979-01-12 1979-01-12 Ozone deodorization equipment Expired JPS5933011B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP54001283A JPS5933011B2 (en) 1979-01-12 1979-01-12 Ozone deodorization equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP54001283A JPS5933011B2 (en) 1979-01-12 1979-01-12 Ozone deodorization equipment

Publications (2)

Publication Number Publication Date
JPS5594622A JPS5594622A (en) 1980-07-18
JPS5933011B2 true JPS5933011B2 (en) 1984-08-13

Family

ID=11497118

Family Applications (1)

Application Number Title Priority Date Filing Date
JP54001283A Expired JPS5933011B2 (en) 1979-01-12 1979-01-12 Ozone deodorization equipment

Country Status (1)

Country Link
JP (1) JPS5933011B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102949922A (en) * 2011-08-24 2013-03-06 苏州仕净环保设备有限公司 Exhaust gas purification tower and exhaust gas treatment system using same
US9833820B2 (en) 2012-09-26 2017-12-05 Sms Meer Gmbh Deoxidation of cross-rolled hollow blocks

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61111525U (en) * 1984-12-21 1986-07-15
JP4522286B2 (en) * 2005-02-17 2010-08-11 三菱電機株式会社 Deodorizing device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102949922A (en) * 2011-08-24 2013-03-06 苏州仕净环保设备有限公司 Exhaust gas purification tower and exhaust gas treatment system using same
US9833820B2 (en) 2012-09-26 2017-12-05 Sms Meer Gmbh Deoxidation of cross-rolled hollow blocks

Also Published As

Publication number Publication date
JPS5594622A (en) 1980-07-18

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