JPH0317559B2 - - Google Patents

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Publication number
JPH0317559B2
JPH0317559B2 JP61303892A JP30389286A JPH0317559B2 JP H0317559 B2 JPH0317559 B2 JP H0317559B2 JP 61303892 A JP61303892 A JP 61303892A JP 30389286 A JP30389286 A JP 30389286A JP H0317559 B2 JPH0317559 B2 JP H0317559B2
Authority
JP
Japan
Prior art keywords
membrane
tank
ammonia
wastewater
nitrification
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 - Lifetime
Application number
JP61303892A
Other languages
Japanese (ja)
Other versions
JPS63158197A (en
Inventor
Takayuki Suzuki
Norio Yamada
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.)
Ebara Corp
Ebara Research Co Ltd
Original Assignee
Ebara Research Co Ltd
Ebara Infilco 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 Ebara Research Co Ltd, Ebara Infilco Co Ltd filed Critical Ebara Research Co Ltd
Priority to JP61303892A priority Critical patent/JPS63158197A/en
Publication of JPS63158197A publication Critical patent/JPS63158197A/en
Publication of JPH0317559B2 publication Critical patent/JPH0317559B2/ja
Granted legal-status Critical Current

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  • Separation Using Semi-Permeable Membranes (AREA)
  • Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
  • Water Treatment By Electricity Or Magnetism (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、し尿系汚水、畜産廃水、ごみ埋立地
浸出汚水などのアンモニアを含有する廃水の窒素
を生物学的手段と物理化学的手段を効率的に利用
して省エネルギー的に除去する方法に関するもの
である。 〔従来の技術及びその問題点〕 し尿系汚水を活性汚泥を用いて硝化・脱窒処理
したのち、沈殿槽の代りにUF膜(限外過膜)
を用いて活性汚泥濃縮液と透過水とに分離し、濃
縮分離された活性汚泥は活性汚泥処理槽(脱窒
槽)に返送すると共に、透過水は活性炭処理を行
い、更にリン酸吸着処理を行つた後処理水として
放流されている。即ち、原水を前記濃縮汚泥と共
に第1反応槽(第1脱窒槽)に供給して脱窒処理
を行つた後、曝気槽に導入して硝化処理を行な
い、この処理液を第2反応槽(第2脱窒槽)を経
て限外過循環槽に導き、該限外過循環槽中の
液を限外過機に循環せしめて濃縮活性汚泥と透
過液とに分離し、濃縮活性汚泥の一部は前述のと
おり脱窒槽に返送すると共に残部は限外過循環
槽に循環せしめている。そして透過液は前述のと
おり活性炭処理などが施こされた後処理水として
排出されている(三井造船エンジニアリング株式
会社;し尿の無希釈アスメツクス)。 この技術は沈殿池の代りにUF膜を用いること
により高濃度の活性汚泥でも安定して固液分離を
行うことができ、また生物処理で残留した
CODMoも分離できるのでCODMo除去のための凝
集処理が省略でき、更にUF膜によつてSSが完全
に分離されるのでし尿系汚水処理で一般的に利用
されていた砂過装置も不要であるという利点が
ある。 しかしながら、UF膜を用いて活性汚泥及び溶
解性高分子物質を分離濃縮するに際しては、UF
膜内の濃度勾配による透過抵抗の上昇及び膜汚染
を防止して所定の透過水量を確保するため極めて
多量の活性汚泥混合液を高圧で循環しており、こ
の循環に消費される電気エネルギーは多大であ
り、廃水処理費用の大きな割合を占めている。 一方、生物処理工程(脱窒工程及び曝気(硝
化)工程)においても硝化工程において生成した
NOXを廃水中のBODを利用して脱窒するため、
大量の硝化液が前段の脱窒槽に循環されており、
この循環に消費されるエネルギーも少なくない。 〔発明が解決しようとする問題点〕 本発明は上記従来技術における問題点を解決
し、省エネルギー的なアンモニア含有廃水の処理
方法を提供するものである。 〔問題点を解決するための手段〕 本発明は、生物学的手段と物理化学的手段とを
用いて塩素イオンを含むアンモニア含有廃水中の
アンモニアを実質的に無希釈で除去する方法にお
いて、該廃水および硝化液の流入する脱窒工程の
活性汚泥混合液を膜分離装置を経由して硝化工程
に移送しアンモニアを硝化した後、前記脱窒工程
に流下せしめて脱窒すると共に、該膜分離装置の
透過水中に残留するアンモニアを該透過水中に存
在する塩素イオンを利用して電解処理することを
特徴とするアンモニア含有廃水の処理方法であつ
て、脱窒槽の処理液を膜分離装置を経由してその
濃縮液を硝化槽(曝気槽)に導入すると共に、透
過水の電解処理装置を付することによつて、上記
問題点を解決したものである。 本発明は、膜分離装置を介在した従来とは逆の
循環(脱窒槽→硝化槽)径路を利用することによ
り、従来法では二本立になつていた循環工程〔生
物処理;曝気槽(硝化槽)→第1反応槽(脱窒
槽)、膜分離:限外濾過槽→限外濾過機→限外
過槽〕を一本化し、循環に要する動力費並びに設
備を減少しようとするものである。 さらに本発明では廃水に含有されているCl-
電気分解してガス化し、膜透過水中に残留する
NH3を処理する電解処理が組み合わされている
が、生物処理工程で循環して硝化、脱窒すること
によつて透過水中のNH3−N濃度を大幅に低減
できるため、外部からNaCl、海水などのCl-を供
給しなくても、廃水がもともと含有しているCl-
だけで生物処理で残留するアンモニアを分解する
ことができる。 本発明の実施態様を第1図を参照しつつ説明す
る。廃水1は嫌気的条件下にある脱窒槽2に流入
し、硝化槽3から溢流し流入する硝化液とともに
撹拌され、該硝化液中のNOXは廃水中のBOD成
分あるいは外部から添加されたアルコールなどを
還元剤として脱窒されN2ガスになる。脱窒槽2
の混合液は膜分離装置6を経由して硝化槽3に循
環され、液中のアンモニアが硝化されてNOX
なり隔壁4を越えて脱窒槽2に溢流する。 循環液5の一部は膜分離装置6から透過され、
それに対応して循環液のMLSSが濃縮される。循
環量に対する透過水量は微々たるものであるた
め、MLSSの濃度上昇はわずかである。 透過水7は電解処理工程8に導かれ、液中の
Cl-から生成されるCl2によつて透過水中のNH3
COD成分、色度成分が酸化分解される。 NH3の分解のためのCl2はNH3−Nの10倍程度
あればよい。 電解処理では分解できなかつたCOD成分は、
図示していないが活性炭処理で除去することがで
きる。 本発明の電解処理水10にはCl2が含有されて
いるので、その濃度が十分な場合には処理水の
Cl2滅菌設備を省略することができる。 一方、残留Cl2濃度が高すぎて処理水10の放
流に支障がある場合には、活性炭処理工程を配置
して、電解処理水10の一部あるいはすべてを活
性炭に通水すればよい。 廃水のBOD/NH3−Nの比が約3.0よりも小さ
い場合には、廃水中のBODのみでは硝化槽3か
ら流入するNO3を脱窒するのに不十分となるの
で、メタノール9などの還元剤の注入設備を脱窒
槽に配備して不足分を補給する必要がある。 生物処理で生成される余剰汚泥11の引き抜き
は硝化槽3から引き抜くと、汚泥中にNOXが含
有されているので、汚泥処理工程12における腐
敗を防止することができる。 汚泥はポリマーのみでも脱水できるが、例えば
塩化第2鉄などの無機凝集剤を用いれば、汚泥の
他に高分子のCOD成分も凝集されて脱水泥とと
もに排除されるので、生物処理工程における
CODの濃縮濃度を減少することができ、膜に対
するCOD負荷を軽減することができる。 本発明では、また第2図に示すように、膜分離
装置6から吐出される循環液5の出口にエジエク
ター15を配備して酸素の供給を行うこともでき
る。しかしながら、高負荷でNH3の処理を行う
場合には、エジエクター15で供給される酸素の
みでは不足するので、別にブロワー18などのエ
アレーシヨン設備を配備しておくことが必要であ
る。 廃水にリンが含有されていて、その除去が必要
な場合には次の様な手段を少なくとも一つ本発明
に付加すればよい。 廃水に生物処理の前段で無機凝集剤を添加し
てリンを不溶化し、固液分離する手段。 生物処理工程に無機凝集剤を添加して不溶化
し、余剰汚泥とともに引き抜く手段。 膜透過以降の液中のリンを凝集固液分離ある
いは吸着する手段。 〔実施例〕 UF膜分離装置を配備していない第1図に示す
生物処理槽(透明アクリル製:20)を用いて除
渣し尿、養豚廃水およびゴミ埋立地浸出汚水を水
温25℃で連続的に硝化、脱窒処理するとともに、
脱窒槽の活性汚泥混合液を回分的に平膜型UF膜
(分画分子量15000)試験装置で分離し、濃縮液は
硝化槽に注入し、透過水は電解処理装置に供し
た。電解処理装置は、活性炭を充填した1の槽
に陽極として白金板、陰極としてステンレス板を
用いて直流で処理するものを用いた。 し尿、養豚廃水、ゴミ埋立地浸出汚水の処理条
件を表1に、処理結果をそれぞれ表2、3、4に
示す。 また表示していないがMF(マイクロフイルタ
ー0.1μ)膜を用いて得た循環液の透過水の電解処
理を表1に示す条件と同条件で行つたところ
NH3の除去率はUF膜を使用した場合とほとんど
同等であつたが、電解処理水のCODは大幅に上
昇した。これは透過水のCODがUF膜に比べMF
膜の方が3〜4倍高かつたからである。
[Industrial Application Field] The present invention is an energy saving method that efficiently uses biological and physicochemical means to remove nitrogen from ammonia-containing wastewater such as human waste water, livestock wastewater, and landfill leachate wastewater. This article relates to a method of removing [Conventional technology and its problems] After nitrifying and denitrifying human waste water using activated sludge, a UF membrane (ultrafiltration membrane) is used instead of a settling tank.
The concentrated and separated activated sludge is returned to the activated sludge treatment tank (denitrification tank), and the permeated water is treated with activated carbon and further subjected to phosphoric acid adsorption treatment. The water is then discharged as treated water. That is, raw water is supplied to the first reaction tank (first denitrification tank) together with the thickened sludge to perform denitrification treatment, then introduced into the aeration tank to perform nitrification treatment, and this treated liquid is transferred to the second reaction tank (first denitrification tank). The liquid in the ultrafiltration tank is circulated through the ultrafiltration machine and separated into concentrated activated sludge and permeated liquid, and a part of the concentrated activated sludge is is returned to the denitrification tank as described above, and the remainder is circulated to the ultrafiltration tank. As mentioned above, the permeate is treated with activated carbon and then discharged as treated water (Mitsui Engineering & Shipbuilding Engineering Co., Ltd.; Asmex, undiluted human waste). By using a UF membrane instead of a settling tank, this technology can stably perform solid-liquid separation even with highly concentrated activated sludge.
Since COD Mo can also be separated, the coagulation treatment for removing COD Mo can be omitted, and since SS is completely separated by the UF membrane, there is no need for sand filter equipment, which is commonly used in night soil wastewater treatment. There is an advantage to having one. However, when separating and concentrating activated sludge and soluble polymer substances using a UF membrane, the UF
In order to prevent increases in permeation resistance and membrane contamination due to concentration gradients within the membrane, and to ensure a predetermined amount of permeated water, an extremely large amount of activated sludge mixture is circulated at high pressure, and a large amount of electrical energy is consumed in this circulation. and accounts for a large proportion of wastewater treatment costs. On the other hand, in the biological treatment process (denitrification process and aeration (nitrification) process),
To denitrify NO X using BOD in wastewater,
A large amount of nitrification liquid is circulated to the denitrification tank in the previous stage.
This circulation consumes a considerable amount of energy. [Problems to be Solved by the Invention] The present invention solves the problems in the prior art described above and provides an energy-saving method for treating ammonia-containing wastewater. [Means for Solving the Problems] The present invention provides a method for removing ammonia from ammonia-containing wastewater containing chloride ions substantially without dilution using biological means and physicochemical means. The activated sludge mixture from the denitrification process into which wastewater and nitrifying solution flow is transferred to the nitrification process via a membrane separation device to nitrify ammonia, and then flowed down to the denitrification process for denitrification and the membrane separation process. A method for treating ammonia-containing wastewater, characterized by electrolytically treating ammonia remaining in the permeated water of the device using chlorine ions present in the permeated water, wherein the treated liquid in the denitrification tank is passed through a membrane separation device. The above-mentioned problems were solved by introducing the concentrated liquid into a nitrification tank (aeration tank) and by attaching an electrolytic treatment device for permeated water. The present invention uses a reverse circulation path (denitrification tank → nitrification tank) with a membrane separation device in between. ) → first reaction tank (denitrification tank), membrane separation: ultrafiltration tank → ultrafiltration machine → ultrafiltration tank] to reduce power costs and equipment required for circulation. Furthermore, in the present invention, Cl - contained in wastewater is electrolyzed and gasified, and remains in the membrane-permeated water.
Electrolytic treatment is combined to treat NH3 , but the NH3 -N concentration in permeated water can be significantly reduced by circulating nitrification and denitrification in the biological treatment process. Even if Cl - such as Cl - is not supplied, the wastewater originally contains Cl -
Only biological treatment can decompose residual ammonia. An embodiment of the present invention will be described with reference to FIG. The wastewater 1 flows into the denitrification tank 2 under anaerobic conditions and is stirred together with the nitrification liquid that overflows from the nitrification tank 3. NO It is denitrified using a reducing agent such as N2 gas. Denitrification tank 2
The mixed liquid is circulated to the nitrification tank 3 via the membrane separator 6, and the ammonia in the liquid is nitrified and becomes NOx , which overflows over the partition wall 4 into the denitrification tank 2. A part of the circulating fluid 5 is permeated from the membrane separator 6,
The MLSS of the circulating fluid is correspondingly concentrated. Since the amount of permeated water is small compared to the amount of circulation, the increase in MLSS concentration is small. The permeated water 7 is led to an electrolytic treatment step 8, and the water in the liquid is
NH3 in permeate water by Cl2 generated from Cl- ,
COD components and chromaticity components are oxidized and decomposed. The amount of Cl 2 for decomposing NH 3 only needs to be about 10 times that of NH 3 -N. COD components that could not be decomposed by electrolytic treatment are
Although not shown, it can be removed by activated carbon treatment. Since the electrolytically treated water 10 of the present invention contains Cl2 , if the concentration is sufficient, the treated water
Cl2 sterilization equipment can be omitted. On the other hand, if the residual Cl 2 concentration is too high and there is a problem in discharging the treated water 10, an activated carbon treatment step may be arranged and part or all of the electrolyzed water 10 may be passed through the activated carbon. If the ratio of BOD/NH 3 -N in the wastewater is less than about 3.0, the BOD in the wastewater alone will be insufficient to denitrify the NO 3 flowing in from the nitrification tank 3, so methanol 9 etc. It is necessary to install reducing agent injection equipment in the denitrification tank to replenish the shortage. When the surplus sludge 11 produced by biological treatment is extracted from the nitrification tank 3, NOx is contained in the sludge, so that putrefaction in the sludge treatment step 12 can be prevented. Sludge can be dehydrated using only polymers, but if an inorganic flocculant such as ferric chloride is used, polymeric COD components will be flocculated in addition to the sludge and removed along with the dehydrated sludge, making it an effective material in the biological treatment process.
The concentrated concentration of COD can be reduced, and the COD load on the membrane can be reduced. In the present invention, as shown in FIG. 2, an ejector 15 can also be provided at the outlet of the circulating fluid 5 discharged from the membrane separator 6 to supply oxygen. However, when processing NH 3 under high load, the oxygen supplied by the ejector 15 alone is insufficient, so it is necessary to separately provide aeration equipment such as a blower 18. If wastewater contains phosphorus and it is necessary to remove it, at least one of the following means may be added to the present invention. A method of adding an inorganic flocculant to wastewater before biological treatment to insolubilize phosphorus and separate solid-liquid. A method of adding an inorganic flocculant to the biological treatment process to make it insolubilized and then pulling it out along with excess sludge. A means of coagulating solid-liquid separation or adsorption of phosphorus in the liquid after it passes through the membrane. [Example] Using the biological treatment tank (made of transparent acrylic: 20) shown in Figure 1, which is not equipped with a UF membrane separation device, filtered human waste, pig wastewater, and landfill leachate sewage were continuously treated at a water temperature of 25°C. In addition to nitrification and denitrification treatment,
The activated sludge mixture in the denitrification tank was separated batchwise using a flat-membrane UF membrane (molecular weight cutoff 15,000) test device, the concentrated liquid was injected into the nitrification tank, and the permeated water was sent to an electrolytic treatment device. The electrolytic treatment apparatus used was one in which one tank filled with activated carbon was treated with a direct current using a platinum plate as an anode and a stainless steel plate as a cathode. The treatment conditions for human waste, pig farm wastewater, and landfill leachate sewage are shown in Table 1, and the treatment results are shown in Tables 2, 3, and 4, respectively. Although not shown, electrolytic treatment of permeated water of circulating fluid obtained using a MF (microfilter 0.1μ) membrane was performed under the same conditions as shown in Table 1.
Although the NH 3 removal rate was almost the same as when using the UF membrane, the COD of the electrolytically treated water increased significantly. This means that the COD of permeated water is MF compared to UF membrane.
This is because the membrane was 3 to 4 times more expensive.

【表】 加した。
[Table] Added.

【表】【table】

【表】【table】

〔効果〕〔effect〕

従来の膜処理および生物処理のための2本
立の循環を1本化したので、循環のための動
力、設備の減少分の運転費、建設費の節減がで
きる。 さらに循環水吐出口にエジエクターを配備す
ることによつて酸素の供給も行うことができ
る。 従来の第2反応槽(第2脱窒槽)をコンパク
トな電解処理装置におきかえることができた。 生物処理工程混合液と膜に供給される混合液
のMLSS濃度がほとんど同一であるため、膜に
対するMLSS負荷を従来よりも軽減することが
できる。 UF膜によつてSSが完全に除去されるので、
SSによる電解処理のトラブルが解消される。 廃水のNH3が硝化槽からの流下液で希釈さ
れて透過水のNH3−N濃度が大幅に低下する
ため、外部からCl-を補給せずに廃水自体のCl-
でも透過水の電解処理を行うことができる。 電解処理によつてNH3の他COD成分、色度
成分も同時に処理することができ、また生成し
たCl2によつて処理水の滅菌が行われる。
Since the conventional dual circulation systems for membrane treatment and biological treatment have been combined into one, it is possible to reduce power for circulation, operating costs due to the reduction in equipment, and construction costs. Furthermore, by providing an ejector at the circulating water outlet, oxygen can also be supplied. The conventional second reaction tank (second denitrification tank) could be replaced with a compact electrolytic treatment device. Since the MLSS concentration of the biological treatment process mixture and the mixture supplied to the membrane are almost the same, the MLSS load on the membrane can be reduced compared to conventional methods. SS is completely removed by the UF membrane, so
Problems with electrolytic treatment caused by SS are resolved. The NH 3 in the wastewater is diluted with the effluent from the nitrification tank, and the NH 3 −N concentration in the permeate water is significantly reduced .
However, electrolytic treatment of permeated water can be performed. By electrolytic treatment, COD components and chromaticity components as well as NH 3 can be treated at the same time, and the Cl 2 produced sterilizes the treated water.

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

第1図は本発明方法を説明するためのフロー概
略図、第2図は膜分離装置6からの循環液出口に
設けるエジエクタを説明するための図である。 1……原水、2……脱窒槽、3……硝化槽、4
……隔壁、6……膜分離装置、8……電解処理工
程、9……還元剤、10……処理水、12……汚
泥処理工程、14……脱水液、15……エジエ
クター、18……ブロワー。
FIG. 1 is a schematic flow diagram for explaining the method of the present invention, and FIG. 2 is a diagram for explaining an ejector provided at the outlet of the circulating liquid from the membrane separation device 6. 1...Raw water, 2...Denitrification tank, 3...Nitrification tank, 4
... Partition wall, 6 ... Membrane separation device, 8 ... Electrolytic treatment step, 9 ... Reducing agent, 10 ... Treated water, 12 ... Sludge treatment step, 14 ... Dehydration liquid, 15 ... Ejector, 18 ... ...Blower.

Claims (1)

【特許請求の範囲】 1 生物学的手段と物理化学的手段とを用いて塩
素イオンを含むアンモニア含有廃水中のアンモニ
アを実質的に無希釈で除去する方法において、該
廃水および硝化液の流入する脱窒工程の活性汚泥
混合液を膜分離装置を経由して硝化工程に移送し
アンモニアを硝化した後、前記脱窒工程に流下せ
しめて脱窒すると共に、該膜分離装置の透過水中
に残留するアンモニアを該透過水中に存在する塩
素イオンを利用して電解処理することを特徴とす
るアンモニア含有廃水の処理方法。 2 膜分離装置から硝化工程に移送する液をエジ
エクターに通過せしめることにより硝化工程への
酸素を供給する特許請求の範囲第1項記載のアン
モニア含有廃水の処理方法。
[Scope of Claims] 1. A method for removing ammonia in ammonia-containing wastewater containing chloride ions substantially without dilution using biological means and physicochemical means, wherein said wastewater and nitrification solution are The activated sludge mixture in the denitrification process is transferred to the nitrification process via a membrane separation device to nitrify ammonia, and then flowed down to the denitrification process to be denitrified and remain in the permeated water of the membrane separation device. A method for treating ammonia-containing wastewater, comprising electrolytically treating ammonia using chlorine ions present in the permeated water. 2. The method for treating ammonia-containing wastewater according to claim 1, wherein oxygen is supplied to the nitrification process by passing the liquid transferred from the membrane separator to the nitrification process through an ejector.
JP61303892A 1986-12-22 1986-12-22 Treatment of ammonia-containing waste water Granted JPS63158197A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61303892A JPS63158197A (en) 1986-12-22 1986-12-22 Treatment of ammonia-containing waste water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61303892A JPS63158197A (en) 1986-12-22 1986-12-22 Treatment of ammonia-containing waste water

Publications (2)

Publication Number Publication Date
JPS63158197A JPS63158197A (en) 1988-07-01
JPH0317559B2 true JPH0317559B2 (en) 1991-03-08

Family

ID=17926518

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61303892A Granted JPS63158197A (en) 1986-12-22 1986-12-22 Treatment of ammonia-containing waste water

Country Status (1)

Country Link
JP (1) JPS63158197A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022186101A1 (en) 2021-03-02 2022-09-09 帝人株式会社 Curing agent composition for thermosetting resin, epoxy resin composition, and fiber-reinforced composite material

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE463364B (en) * 1988-06-03 1990-11-12 Ecocure Ab PROCEDURES FOR THE REMOVAL OF NAVIGATES FROM RAAVATTEN

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60232296A (en) * 1984-04-28 1985-11-18 Sanki Eng Co Ltd Treatment of organic waste water containing nitrogen compound
JPS60255198A (en) * 1984-05-31 1985-12-16 Ebara Infilco Co Ltd Biological treatment of waste water

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022186101A1 (en) 2021-03-02 2022-09-09 帝人株式会社 Curing agent composition for thermosetting resin, epoxy resin composition, and fiber-reinforced composite material

Also Published As

Publication number Publication date
JPS63158197A (en) 1988-07-01

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