JPS6035165B2 - Ozone decolorization and deodorization method - Google Patents
Ozone decolorization and deodorization methodInfo
- Publication number
- JPS6035165B2 JPS6035165B2 JP55018166A JP1816680A JPS6035165B2 JP S6035165 B2 JPS6035165 B2 JP S6035165B2 JP 55018166 A JP55018166 A JP 55018166A JP 1816680 A JP1816680 A JP 1816680A JP S6035165 B2 JPS6035165 B2 JP S6035165B2
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- JP
- Japan
- Prior art keywords
- gas
- ozone
- activated carbon
- cleaning
- water
- 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
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- Treating Waste Gases (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
Description
【発明の詳細な説明】
本発明は、汚濁物処理場から発生する悪臭ガスを、同処
理場からの排水のオゾンによる脱色浄化処理の排ガス中
の未反応オゾンにより効率的に浄化するための方法に関
する。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a method for efficiently purifying malodorous gas generated from a pollutant treatment plant using unreacted ozone in the exhaust gas of decolorizing and purifying wastewater from the same treatment plant using ozone. Regarding.
下水処理場、し尿処理場などの汚濁物処理場においては
、汚染物を必要において水で希釈しながら、嫌気または
好気微生物処理あるいは化学処理などにより汚濁物を分
解処理し、更に沈澱処理して沈澱物をスラツジとして廃
棄する一方、上燈液(処理水)については更に残存する
有機物による着色を除くためオゾン含有空気と気液接触
する処理が広く行われている。In pollutant treatment plants such as sewage treatment plants and human waste processing plants, pollutants are decomposed by anaerobic or aerobic microbial treatment or chemical treatment, diluting them with water if necessary, and then subjected to sedimentation treatment. While the precipitate is disposed of as sludge, the top lighting solution (treated water) is also widely treated by bringing it into gas-liquid contact with ozone-containing air in order to remove coloring caused by residual organic matter.
しかしながら、このオゾン処理におけるオゾン吸収効率
は90%程度であり、排水の水質基準を高く設定すれば
、オゾン吸収効率は更に低下する。したがって、オゾン
処理における気液接触後の排ガス中には少なからぬ量、
たとえば数百ppmのオゾンが未反応で残っている。こ
の未反応オゾンは、環境衛生上、直接大気中に放出する
ことはできないため、熱分解、活性炭分解、触媒分解、
薬液洗浄などにより処理されていた。しかし、これらの
オゾンの除去処理法は必ずしも満足すべきものとは云い
難い。たとえば、従来、活性炭分解塔は、保守点検が簡
単なため最も広く用いられているが、オゾン4〜5夕に
対して活性炭1夕が炭酸ガスあるいは一酸化炭素として
消費されるため、処理コストが高いという欠点がある。
一方、汚濁物処理場においては、汚濁物自体の分解によ
り、硫化水素、メルカプタン類、チオェーテル類、アン
モニア、ァミン類の還元性悪臭成分を含む悪臭ガスが発
生するため、これを浄化して無臭ガスとして大気中に放
出する必要がある。However, the ozone absorption efficiency in this ozone treatment is about 90%, and if the water quality standards for wastewater are set high, the ozone absorption efficiency will further decrease. Therefore, a considerable amount of
For example, several hundred ppm of ozone remains unreacted. This unreacted ozone cannot be released directly into the atmosphere for environmental hygiene reasons, so it can be decomposed by thermal decomposition, activated carbon decomposition, catalytic decomposition, etc.
It was treated with chemical cleaning, etc. However, these ozone removal treatment methods are not necessarily satisfactory. For example, activated carbon decomposition towers have traditionally been the most widely used because they are easy to maintain and inspect, but treatment costs are high because one night of activated carbon is consumed as carbon dioxide or carbon monoxide for every four to five nights of ozone. It has the disadvantage of being expensive.
On the other hand, in pollutant treatment plants, the decomposition of pollutants themselves generates foul-smelling gas containing reducing foul-smelling components such as hydrogen sulfide, mercaptans, thioethers, ammonia, and amines. must be released into the atmosphere as air.
本発明者らは、この悪臭ガスの浄化方法として、一つの
有効な方法を既に提案している(昭和54玉特許豚第7
7673号)。すなわち、その悪臭ガスの浄化方法は、
硫化水素を含む悪臭ガスを、酸素の存在下にアルカリ性
活性炭懸濁液により洗浄する第1洗浄工程、酸化剤含有
液により洗浄する第2洗浄工程、アルカリ液により洗浄
する第3洗浄工程で順次、洗浄処理することを特徴とす
るものである。しかして、この方法によれば第1工程に
おし、て悪臭成分中で比較的酸化されやすい硫化水素が
分子状酸素により酸化され、第2工程では比較的難酸化
性のチオェーテル類、メルカブタン類などが酸化され、
酸化剤の分解により生ずる塩素等の酸化性ガスは第3工
程で吸収される。したがってこの方法によれば少し、薬
液の使用量で効果的な悪臭ガスの浄化が期待できる。本
発明は上記したオゾン除去処理方法と、悪臭ガスの浄化
方法を組合せて、両者をともに効率化せんとするもので
ある。The present inventors have already proposed an effective method for purifying this foul-smelling gas (No.
No. 7673). In other words, the method for purifying the foul-smelling gas is
A first cleaning step in which the malodorous gas containing hydrogen sulfide is cleaned with an alkaline activated carbon suspension in the presence of oxygen, a second cleaning step in which the oxidizing agent-containing liquid is used to clean the malodorous gas, and a third cleaning step in which the alkaline solution is used to clean the foul-smelling gas. It is characterized by a cleaning treatment. According to this method, in the first step, hydrogen sulfide, which is relatively easily oxidized among malodorous components, is oxidized by molecular oxygen, and in the second step, relatively oxidizable thioethers and mercaptans are oxidized. etc. are oxidized,
Oxidizing gases such as chlorine produced by decomposition of the oxidizing agent are absorbed in the third step. Therefore, according to this method, effective purification of malodorous gas can be expected with a small amount of chemical solution used. The present invention combines the above-described ozone removal treatment method and malodorous gas purification method to improve the efficiency of both.
すなわち本発明のオゾン脱色脱臭方法は汚濁物処理場か
ら発生する還元性悪臭ガスと、汚濁物処理水のオゾン脱
色浄化で生じた未反応オゾン含有ガスとを混合し、混合
ガスを、アルカリ性活性炭懸濁液との気液接触、酸化剤
含有液との気液接触、含まれる酸化性ガスを除去するた
めの固体活性炭との気固接触により、順次、浄化処理す
ることを特徴とするものである。本発明の方法は、上記
した三段法による悪臭ガスの浄化方法において、第1段
階での彼処理ガスと未反応オゾン含有ガスの混合ガスを
用い、第3段階でのアルカリ液洗浄の代りに固体活性炭
との気固接触浄化処理を用いるものである。本発明方法
においては、汚濁物処理水のオゾン脱色浄化で生じた未
反応オゾン含有ガスを還元性悪臭ガスの浄化に効果的に
使用して、オゾン濃度を低下したのちに活性炭との気固
接触に付すので、第3段階での活性炭の消費量が著しく
低下され、また脱臭洗浄排水の無臭化ならびにCOD低
下も達成される効果がある。以下、本発明を実施するた
めの装置系の一例の配置図を示す添付図面を参照しつつ
、本発明の一実施態様を更に詳細に説明する。That is, the ozone decolorization and deodorization method of the present invention mixes reducing malodorous gas generated from a pollutant treatment plant and unreacted ozone-containing gas generated by ozone decolorization and purification of pollutant-treated water, and the mixed gas is suspended in alkaline activated carbon. It is characterized by sequential purification treatment through gas-liquid contact with a turbid liquid, gas-liquid contact with an oxidizing agent-containing liquid, and gas-solid contact with solid activated carbon to remove the oxidizing gas contained. . The method of the present invention uses a mixed gas of the treated gas in the first stage and unreacted ozone-containing gas in the three-stage method described above, and replaces the alkaline solution cleaning in the third stage. This method uses gas-solid contact purification treatment with solid activated carbon. In the method of the present invention, unreacted ozone-containing gas generated by ozone decolorization purification of pollutant-treated water is effectively used to purify reducing odor gas, and after reducing the ozone concentration, it is brought into gas-solid contact with activated carbon. , the amount of activated carbon consumed in the third stage is significantly reduced, and the deodorized cleaning wastewater is made odorless and COD is reduced. DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the present invention will be described in more detail below with reference to the accompanying drawings showing a layout of an example of an apparatus system for carrying out the present invention.
図面にしたがい、下水処理場、し尿処理場等の汚濁物処
理場から発生した硫化水素、メチルメルカプタン、硫化
メチル、アンモニア、メチルアミンなどの還元性悪臭成
分を含有する悪臭ガス1は、後述するオゾン脱色浄化装
置から配管2を経て送られる未反応オゾン含有ガスとと
もに洗浄方式による脱臭装置本体3に導入される。According to the drawing, malodorous gas 1 containing reducing malodorous components such as hydrogen sulfide, methyl mercaptan, methyl sulfide, ammonia, and methylamine generated from a pollutant treatment plant such as a sewage treatment plant or human waste treatment plant is ozone as described below. Together with the unreacted ozone-containing gas sent from the decolorization and purification device via piping 2, it is introduced into the main body 3 of the deodorization device using a cleaning method.
導入された混合ガスは、まず、ラシヒリング等の充填材
4を充填した第1洗浄部5で、配管6ならびにスプレー
ノズル7を通じて導入される水により洗浄され、悪臭ガ
ス中のアンモニア、トリメチルアミンなどの水溶性の大
きな成分が吸収除去される。これら成分を吸収した洗浄
水は、貯留部8、配管9を通して系外へ排出される。第
1洗浄部5を通過したガスはェリミネーター10を通り
、洗浄水と分離されて、同機に充填材4を充填した第2
洗浄部11に導入される。第2洗浄部11では、糟12
内において平均粒度が200メッシュより小さい活性炭
を約1重量%の濃度、pH9〜11好ましくは1栃華度
に調整されたアルカリ性活性炭懸濁液13がポンプ14
、配管15を経てスプレーノズル7から贋霧され、これ
により第1洗浄部からのガス中の主として硫化水素がア
ルカリ性情性炭懸濁液中に吸収され、同ガス中に含まれ
る未反応オゾンおよび分子状酸素の存在下に酸化される
。硫化水素が酸化されて生成したチオ硫酸イオン等を含
むアルカリ性情性炭懸濁液は、貯留部16、配管17を
経てアルカリ性活性炭懸濁液調整槽12に戻される。第
2洗浄部11を出たガスは、未だチオェーブル類、メル
カプタン類などの比較的灘酸化性の成分および負荷の大
きい場合は硫化水素の一部を含むため、ェリミネーター
10を通して充填材4を充填した第3洗浄部21へ導入
される。The introduced mixed gas is first washed by water introduced through piping 6 and spray nozzle 7 in the first cleaning section 5 filled with a filler 4 such as Raschig ring, and water-soluble ammonia, trimethylamine, etc. in the foul-smelling gas are removed. Highly active components are absorbed and removed. The cleaning water that has absorbed these components is discharged to the outside of the system through the storage section 8 and piping 9. The gas that has passed through the first cleaning section 5 passes through the eliminator 10 and is separated from the cleaning water.
It is introduced into the cleaning section 11. In the second cleaning section 11, the dirt 12
An alkaline activated carbon suspension 13 containing activated carbon having an average particle size of less than 200 mesh at a concentration of about 1% by weight and adjusted to a pH of 9 to 11 degrees Fahrenheit, preferably 1 degree Fahrenheit, is pumped into the pump 14.
, from the spray nozzle 7 via the pipe 15, whereby mainly hydrogen sulfide in the gas from the first cleaning section is absorbed into the alkaline carbon suspension, and unreacted ozone and Oxidized in the presence of molecular oxygen. The alkaline activated carbon suspension containing thiosulfate ions and the like produced by oxidizing hydrogen sulfide is returned to the alkaline activated carbon suspension adjustment tank 12 via the storage section 16 and piping 17. Since the gas exiting the second cleaning section 11 still contains relatively oxidizing components such as thioables and mercaptans, and some hydrogen sulfide if the load is large, the gas is passed through the eliminator 10 and filled with the filler 4. It is introduced into the third cleaning section 21.
第3洗浄部21では、糟22内で濃度を調整された、た
とえば次亜塩素酸ナトリウム溶液(有効塩素濃度約30
0の9/夕,pH8.9華度)などの酸化剤溶液23が
ポンプ24、配管25を経てスプレーノズル7から散布
される。これによりチオェーテル類等を酸化吸収した酸
化剤溶液は、貯留部26、敵管27を経て槽22へ循環
される。第3洗浄部21を出たガスはェリミネーター1
0を経、更にデミスター28でミストを除去されたのち
、洗浄部本体3を出る。洗浄部本体を出たガスは、第3
洗浄部21での酸化剤の分解により生じた塩素あるいは
未反応オゾンの酸化性ガスを0.5〜2ppm程度含む
。In the third cleaning section 21, for example, a sodium hypochlorite solution (effective chlorine concentration of about 30
An oxidizing agent solution 23 such as oxidizer solution 23 (pH 8.9 Fahrenheit) is sprayed from the spray nozzle 7 via the pump 24 and piping 25. As a result, the oxidizing agent solution that has oxidized and absorbed thioethers and the like is circulated to the tank 22 via the reservoir 26 and the pipe 27. The gas exiting the third cleaning section 21 is transferred to the eliminator 1
0, the mist is further removed by a demister 28, and then exits the cleaning section main body 3. The gas leaving the main body of the cleaning section is
It contains about 0.5 to 2 ppm of oxidizing gas such as chlorine or unreacted ozone generated by decomposition of the oxidizing agent in the cleaning section 21 .
したがってこのガスは、フ。呂ワー30、ダクト31を
通り、活性炭分解塔32内の粒状活性炭の充填層33に
送られ、ここで気固接触して酸化性ガスを除かれて、ほ
ぼ無害無臭のガスとして大気へ放出される。一方、前述
した配管2を通して洗浄部本体3に供給される未反応オ
ゾン含有ガスは以下のようにして得られる。Therefore, this gas is fu. The activated carbon is sent to a packed bed 33 of granular activated carbon in an activated carbon decomposition tower 32 through a boiler 30 and a duct 31, where it undergoes gas-solid contact to remove oxidizing gases and is released into the atmosphere as an almost harmless and odorless gas. Ru. On the other hand, the unreacted ozone-containing gas supplied to the cleaning section main body 3 through the aforementioned pipe 2 is obtained as follows.
すなわち、オゾン反応塔40の上部には、脱色浄化を目
的として、下水処理水、し尿処理水などの汚濁物処理水
が配管41を通じて導入されオゾン反応塔40内に貯え
られる。一方配管42から導入された空気等の酸素含有
気体は、オゾン発生器43を通過する間にオゾン含有気
体に変換され、更に配管44経てオゾン反応塔40の底
部に設けたディフューザー45から細かい気泡として塔
40内に導入される。これにより塔40内の被処理水は
底部から配管46を通して系外に排出される。一方オゾ
ン反応塔40内でオゾン酸化を受ける汚濁物処理水中に
は、オゾン含有気体の微細気泡との接触により発泡性を
示す物体が含まれており、気泡の上昇に伴ない、液面上
に発泡層を作る。この泡のかたまりは、未反応オゾン含
有気体とともに反応塔40の頂部に接続した配管47を
通して反応塔40から出、消泡塔48に導入される。消
泡塔48では、配管49を通して導入された上水、井戸
水、河川水などの消泡水がスプレーノズル50から散布
され未反応オゾン含有ガスに同伴された泡をこわし、底
部より配管51を通して系外に放出される。一方、泡の
除かれた禾反応オゾン含有ガスはデミスター52を経て
消泡塔48を出、上述したように配管2を経て、洗浄部
本体3に導入される。悪臭ガスのアルカリ性活性炭懸濁
液洗浄に際して悪臭ガスにオゾンを混入すると、オゾン
は効率的に除去される。That is, pollutant-treated water such as treated sewage water and human waste water is introduced into the upper part of the ozone reaction tower 40 through a pipe 41 and stored in the ozone reaction tower 40 for the purpose of decolorization and purification. On the other hand, the oxygen-containing gas such as air introduced from the pipe 42 is converted into an ozone-containing gas while passing through the ozone generator 43, and further passes through the pipe 44 and exits from the diffuser 45 provided at the bottom of the ozone reaction tower 40 as fine bubbles. is introduced into the tower 40. As a result, the water to be treated in the tower 40 is discharged from the bottom through the pipe 46 to the outside of the system. On the other hand, the pollutant-treated water that undergoes ozone oxidation in the ozone reaction tower 40 contains substances that exhibit foaming properties when they come into contact with fine bubbles of ozone-containing gas, and as the bubbles rise, they rise above the liquid surface. Create a foam layer. This mass of foam exits the reaction tower 40 through a pipe 47 connected to the top of the reaction tower 40 together with the unreacted ozone-containing gas and is introduced into the defoaming tower 48 . In the defoaming tower 48, defoaming water such as tap water, well water, river water, etc. introduced through a pipe 49 is sprayed from a spray nozzle 50 to break up the bubbles entrained in the unreacted ozone-containing gas, and the defoaming water is introduced from the bottom through a pipe 51 into the system. released outside. On the other hand, the reacted ozone-containing gas from which bubbles have been removed exits the defoaming tower 48 through the demister 52, and is introduced into the cleaning section main body 3 through the pipe 2 as described above. When ozone is mixed into malodorous gas when cleaning malodorous gas with an alkaline activated carbon suspension, ozone is efficiently removed.
たとえば、オゾンを20ppmの濃度で含有する悪臭ガ
スを1の/mjnの割合で流し、これを3ぞ/mjnの
割合で供給する活性炭濃度1重量%、pHIOのアルカ
リ性活性炭懸濁液とガス流速lm/sec、接触時間2
秒の条件で気液接触した場合、オゾン濃度は20ppm
からlppmへと低下できることが確認されている。す
なわち、ここで消費された未反応オゾンだけ、活性炭分
解塔における活性炭の消費量が低下され、またアルカリ
性活性炭懸濁液中で浄化反応が効率化されるわせである
。上記においては添付増面を参照しつつ、本発明の好ま
しい−実施態様を説明した。For example, a malodorous gas containing ozone at a concentration of 20 ppm is flowed at a rate of 1/mjn, and this is supplied at a rate of 3/mjn with an activated carbon concentration of 1% by weight, an alkaline activated carbon suspension of pHIO, and a gas flow rate of lm. /sec, contact time 2
In the case of gas-liquid contact under conditions of seconds, the ozone concentration is 20 ppm.
It has been confirmed that it can be reduced from 1ppm to 1ppm. That is, the amount of activated carbon consumed in the activated carbon decomposition tower is reduced by the amount of unreacted ozone consumed here, and the purification reaction in the alkaline activated carbon suspension is made more efficient. In the foregoing, preferred embodiments of the invention have been described with reference to the accompanying drawings.
しかし、当業者には、本発明の範囲内で上記態様を種々
改変して実施できることが容易に理解できよう。たとえ
ば、脱臭装置本体3内の第1洗浄部5では、洗浄液とし
て水の代りにアンモニア、アミン類の除去効果の高い酸
溶液を用いることもできるし、この水ないし酸洗浄部を
第2洗浄部11と第3洗浄部21との間に挿入すること
もできる。またこの水ないし酸洗浄部は必須のものでは
なく、省略することもできる。ただしこの場合は、第3
洗浄部21の酸化剤溶液によりアンモニア、アミン類等
が除去され酸化剤溶液の消費量は多くなる。なお、各洗
浄部での洗浄液は、バッチ的あるいは連続的のいずれの
方法で調製しても良く、またオゾン反応塔40は複数個
用いることができることは云うまでもない。上述したよ
うに、本発明によれば、汚濁物処理場からの処理水の脱
色浄化により生ずる未反応オゾンを同処理場から発生す
る悪臭ガスの浄化に利用することにより未反応オゾンの
分解に必要であった活性炭ならびに悪臭ガスの分解に必
要であった酸化剤の双方の使用量を著しく低減し、更に
脱臭洗浄排水の無臭化、COD低下などにも効果があり
、汚濁物処理場の運転が全体として著しく効率できる。However, those skilled in the art will readily understand that the above embodiments can be modified in various ways within the scope of the present invention. For example, in the first cleaning section 5 in the deodorizing device main body 3, an acid solution having a high effect of removing ammonia and amines can be used as the cleaning liquid instead of water, and this water or acid cleaning section can be used in the second cleaning section. 11 and the third cleaning section 21. Further, this water or acid washing section is not essential and can be omitted. However, in this case, the third
Ammonia, amines, etc. are removed by the oxidizing agent solution in the cleaning section 21, and the consumption amount of the oxidizing agent solution increases. Note that the cleaning liquid in each cleaning section may be prepared either batchwise or continuously, and it goes without saying that a plurality of ozone reaction towers 40 can be used. As described above, according to the present invention, unreacted ozone generated by decolorizing and purifying treated water from a pollutant treatment plant is used to purify malodorous gas generated from the same treatment plant, thereby reducing the amount of ozone necessary for decomposing the unreacted ozone. It significantly reduces the usage of both activated carbon and oxidizing agents that were required to decompose malodorous gases, and is also effective in making deodorized cleaning wastewater odorless and reducing COD, making it easier to operate pollutant treatment plants. Overall, it is extremely efficient.
また本発明法による操業は悪臭ガス発生量ならびに未反
応オゾン量の変動に対しても安定であるという特性を有
している。Furthermore, the operation according to the method of the present invention has the characteristic of being stable against fluctuations in the amount of malodorous gas generated and the amount of unreacted ozone.
図面は本発明を実施するための装置系の代表例における
各機器の配置図である。
1・・・原悪臭ガス、3・・・脱臭装置本体、32・・
・活性炭塔、40・・・オゾン反応塔、43・・・オゾ
ン発生器、48・・・消泡塔。The drawing is a layout diagram of each device in a typical example of an apparatus system for carrying out the present invention. 1...Original malodorous gas, 3...Deodorizing device main body, 32...
- Activated carbon tower, 40... Ozone reaction tower, 43... Ozone generator, 48... Defoaming tower.
Claims (1)
物処理水のオゾン脱色浄化で生じた未反応オゾン含有ガ
スとを混合し、混合ガスを、アルカリ性活性炭懸濁液と
の気液接触、酸化剤含有液との気液接触、含まれる酸化
性ガスを除去するための固体活性炭との気固接触により
、順次浄化処理することを特徴とする、オゾン脱色脱臭
方法。1. Mixing reducing malodorous gas generated from a pollutant treatment plant and unreacted ozone-containing gas generated from ozone decolorization purification of pollutant-treated water, and bringing the mixed gas into gas-liquid contact with an alkaline activated carbon suspension; An ozone decolorizing and deodorizing method characterized by sequential purification treatment through gas-liquid contact with an oxidizing agent-containing liquid and gas-solid contact with solid activated carbon to remove the oxidizing gas contained.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55018166A JPS6035165B2 (en) | 1980-02-16 | 1980-02-16 | Ozone decolorization and deodorization method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55018166A JPS6035165B2 (en) | 1980-02-16 | 1980-02-16 | Ozone decolorization and deodorization method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56115619A JPS56115619A (en) | 1981-09-10 |
| JPS6035165B2 true JPS6035165B2 (en) | 1985-08-13 |
Family
ID=11964016
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55018166A Expired JPS6035165B2 (en) | 1980-02-16 | 1980-02-16 | Ozone decolorization and deodorization method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6035165B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58133818A (en) * | 1982-02-01 | 1983-08-09 | Mitsubishi Heavy Ind Ltd | Removing method of malodor utilizing waste ozone |
| US6528014B1 (en) * | 1999-09-13 | 2003-03-04 | Sl Parkhurst Corporation | Foul air eliminator |
| KR100488904B1 (en) * | 2002-05-10 | 2005-05-10 | 박수길 | Method and Apparatus for Remove a Bad Smell |
| US7147822B2 (en) | 2003-07-07 | 2006-12-12 | Sl Parkhurst Corporation | Aerosol odor eliminator |
-
1980
- 1980-02-16 JP JP55018166A patent/JPS6035165B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56115619A (en) | 1981-09-10 |
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