JPH0476757B2 - - Google Patents

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Publication number
JPH0476757B2
JPH0476757B2 JP59237540A JP23754084A JPH0476757B2 JP H0476757 B2 JPH0476757 B2 JP H0476757B2 JP 59237540 A JP59237540 A JP 59237540A JP 23754084 A JP23754084 A JP 23754084A JP H0476757 B2 JPH0476757 B2 JP H0476757B2
Authority
JP
Japan
Prior art keywords
wastewater
phosphorus
aeration
nitrogen
anaerobic
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
JP59237540A
Other languages
Japanese (ja)
Other versions
JPS61118195A (en
Inventor
Toshio Shimooka
Hiroaki Myakoshi
Shuichi Kojima
Toyoichi Yokomaku
Takao Tanihara
Shoichi Hirata
Asao Horiuchi
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.)
Kankyo Engineering Co Ltd
Original Assignee
Kankyo Engineering 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 Kankyo Engineering Co Ltd filed Critical Kankyo Engineering Co Ltd
Priority to JP23754084A priority Critical patent/JPS61118195A/en
Publication of JPS61118195A publication Critical patent/JPS61118195A/en
Publication of JPH0476757B2 publication Critical patent/JPH0476757B2/ja
Granted legal-status Critical Current

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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、嫌気工程および好気工程を含む回分
式の活性汚泥法による排水の生物学的処理方法に
関し、特に排水中の窒素と燐とを同時に生物学的
に処理して排水中から除去する方法に関する。 (従来の技術) 近年、内湾、内海、湖沼等の水域における窒素
および燐による富栄養化現象の進行は、水質汚濁
の主原因として大きな社会問題化し、これらの水
質汚染の原因となる一般家庭および工場排水に対
して、特に排水中に含まれる窒素および燐に対し
て厳しい規制が実施され、そのための排水処理方
法も種々提案されている。 排水処理方法として最も一般的な方法は活性汚
泥法による生物学的処理方法であり、該方法によ
る窒素の除去は、好気条件下でBOD酸化菌と硝
化菌を利用して、排水中の各種窒素化合物を亜硝
酸または硝酸まで酸化する工程と、嫌気条件下で
脱窒菌を利用して、硝化工程で生成した硝酸また
は亜硝酸を窒素ガスに還元する脱窒工程の2工程
からなつている。 また、活性汚泥法により微生物反応を利用する
燐の除去方法は、生物学的燐除去法と呼ばれ、生
物学的処理の嫌気工程で放出された燐を好気工程
で微生物の細胞に過剰に取り込ませて、この燐を
取り込んだ微生物を余剰汚泥の形で処理系外に取
出す方法と、微生物により過剰に摂取された燐を
嫌気条件下で再び放出させて、燐の濃縮液とし、
これを化学的に凝集させて分離除去する方法に大
別されている。 (発明が解決しようとしている問題点) しかしながら、上記の如き従来の活性汚泥法に
より、窒素と燐を同時に除去しようとすること
は、嫌気処理と好気処理という互いに相反する微
生物代謝メカニズムを利用するものであるため、
従来の嫌気工程と好気工程とを組合わせた活性汚
泥法では排水中の窒素と燐とを同時に効率的に除
去することは極めて困難であり、通常は、排水中
の窒素は全体の40〜60%しか除去できず、また燐
では30〜50%程度が除去されるにすぎなかつた。 従つて、可能な限り簡単な方法で且つ効率のよ
い排水の生物学的処理方法が強く要望されている
のが実情である。 本発明者は上述の如き従来技術の欠点を解決
し、上記の要望に応えるべく、排水の生物学的処
理方法について鋭意研究の結果、処理すべき排水
の性質を簡単に制御するのみで、従来の回分式の
排水の生物学的処理装置をそのまま利用して、従
来方法では達成し得なかつた高い効率で排水中の
窒素と燐を容易に且つ低コストで同時に処理し、
除去できることを知見して本発明を完成した。 (問題点を解決するための手段) すなわち、本発明は、嫌気工程および好気工程
を含む回分式の活性汚泥法による排水の生物学的
処理方法において、曝気槽へ導入する排水を嫌気
性貯留槽中に1時間以上滞留させて酸化還元電位
を−150mV以下に制御した後、該排水を曝気槽
に導入し、且つ曝気槽中への排水の流入中は嫌気
撹拌を行い、排水から窒素および燐を同時に除去
することを特徴とする排水の生物学的処理方法で
ある。 本発明を更に詳細に説明すると、本発明が主た
る第1の特徴とする点は、処理すべき排水を従来
の回分式の活性汚泥法により処理するに際して、
処理前にその酸化還元電位を一定の値以下に調整
することおよび第2の特徴点として、このように
調整された排水を曝気槽に流入中は、曝気槽中で
嫌気撹拌を行うことであり、このような特徴点に
より、本発明の目的が主として達成されたもので
ある。 すなわち、本発明者の詳細な研究によれば、処
理すべき原排水を、−150mV以下の曝気条件下に
保持しておき、且つ曝気槽へ流入時の嫌気状態を
保持し曝気槽中で嫌気撹拌を行うことにより、
ATPの加水分解が速やかに進行して燐が放出さ
れ、続いて行う曝気による好気条件下ではATP
が生産され、微生物が燐を過剰に摂取でき、一
方、次いで行う脱窒工程の嫌気条件下では亜硝酸
または硝酸態の窒素が存在するために、ポリリン
酸蓄積微生物は通常の呼吸代謝を維持することが
でき、摂取した燐は放出されず、従つて一連の生
物学的処理工程を通して汚泥の燐含有率が高濃度
に維持され、結果として燐の除去効果が著しく高
く維持されることを知見したものである。 本発明において、処理すべき原排水の酸化還元
電位を一定の値以下、すなわち−150mV以下と
する好ましい方法としては、処理すべき原排水を
曝気槽に注入する前に、一定時間嫌気状態を保つ
方法である。このような方法としては、原排水を
曝気槽に注入する前に貯留槽にて一定時間以上嫌
気状態を保持する方法や、貯留槽中における原排
水の混合撹拌時に曝気をコントロールするかある
いは曝気を行わない等の方法が好ましい。一般的
には、このように嫌気状態を約1時間以上保持す
ることによつて、原排水の酸化還元電位を−
150mV以下とすることができる。 このような原排水の酸化還元電位の測定は、通
常の酸化還元電位計により容易に行うことができ
る。 本発明において、窒素と燐とを同時に処理する
ことができる排水としては、食品工場排水をはじ
めとする工場排水、し尿および下水などの有機性
排水で、窒素と燐とを過剰に含有する排水であれ
ば、いずれの排水をも処理することができる。特
にBOD濃度100mg/以上5000mg/以下で、
BOD/窒素比が3以上の排水であれば、本発明
の処理効果が最も顕著となる。このような有機性
の排水では、通常、曝気等により酸化状態に保つ
操作を行われなければ、容易に嫌気状態を維持す
ることが可能である。具体例を挙げると、家庭下
水A、20倍稀釈のし尿消化脱離液B、製薬工場
C、醸造工場Dの各種排水を種々の量で曝気する
と、曝気中のDOの変化と酸化還元電位との関係
は下記の通りとなり、従つていずれも容易に排水
中のDO値を選定することにより、排水の酸化還
元電位を容易に−150mV以下に制御することが
できる。
(Industrial Application Field) The present invention relates to a biological treatment method for wastewater using a batch activated sludge method including an anaerobic process and an aerobic process, and in particular, the present invention relates to a biological treatment method for wastewater using a batch activated sludge method including an anaerobic process and an aerobic process. and how to remove it from wastewater. (Prior art) In recent years, the progression of eutrophication due to nitrogen and phosphorus in water bodies such as inner bays, inland seas, and lakes has become a major social problem as a main cause of water pollution. Strict regulations have been put in place for factory wastewater, particularly regarding nitrogen and phosphorus contained in the wastewater, and various wastewater treatment methods have been proposed. The most common method for wastewater treatment is the biological treatment method using activated sludge. This method uses BOD oxidizing bacteria and nitrifying bacteria under aerobic conditions to remove various types of nitrogen from wastewater. It consists of two steps: a step in which nitrogen compounds are oxidized to nitrous acid or nitric acid, and a denitrification step in which nitric acid or nitrous acid produced in the nitrification step is reduced to nitrogen gas using denitrifying bacteria under anaerobic conditions. In addition, a method for removing phosphorus that utilizes microbial reactions using the activated sludge method is called a biological phosphorus removal method, in which excess phosphorus released in the anaerobic process of biological treatment is transferred to microbial cells in the aerobic process. The microorganisms that have taken in phosphorus are taken out of the treatment system in the form of surplus sludge, and the excess phosphorus taken up by the microorganisms is released again under anaerobic conditions to form a concentrated phosphorus solution.
There are two main types of methods: chemically agglomerating the particles and separating and removing them. (Problem to be solved by the invention) However, attempting to simultaneously remove nitrogen and phosphorus using the conventional activated sludge method as described above utilizes mutually contradictory microbial metabolic mechanisms of anaerobic treatment and aerobic treatment. Because it is a thing,
It is extremely difficult to efficiently remove nitrogen and phosphorus from wastewater at the same time using the conventional activated sludge method, which combines an anaerobic process and an aerobic process. Only 60% could be removed, and only 30-50% of phosphorus was removed. Therefore, the reality is that there is a strong demand for a biological treatment method for wastewater that is as simple and efficient as possible. In order to solve the above-mentioned drawbacks of the conventional technology and meet the above-mentioned needs, the present inventor has conducted intensive research into a biological treatment method for wastewater, and found that it is possible to simply control the properties of the wastewater to be treated. By using the batch-type wastewater biological treatment equipment of 2015 as is, nitrogen and phosphorus in wastewater can be easily and inexpensively treated at the same time with high efficiency that could not be achieved with conventional methods.
The present invention was completed based on the finding that it can be removed. (Means for Solving the Problems) That is, the present invention provides a biological treatment method for wastewater using a batch activated sludge method including an anaerobic process and an aerobic process, in which wastewater introduced into an aeration tank is stored in an anaerobic storage system. After staying in the tank for over 1 hour and controlling the redox potential to -150mV or less, the wastewater is introduced into the aeration tank, and anaerobic stirring is performed while the wastewater is flowing into the aeration tank to remove nitrogen and nitrogen from the wastewater. This is a biological treatment method for wastewater that is characterized by the simultaneous removal of phosphorus. To explain the present invention in more detail, the first main feature of the present invention is that when wastewater to be treated is treated by the conventional batch activated sludge method,
The oxidation-reduction potential is adjusted to below a certain value before treatment, and the second feature is that while the wastewater thus adjusted is flowing into the aeration tank, anaerobic stirring is performed in the aeration tank. , These features have mainly achieved the object of the present invention. That is, according to detailed research by the present inventor, raw wastewater to be treated is maintained under aeration conditions of −150 mV or less, and the anaerobic state at the time of flow into the aeration tank is maintained, and the anaerobic state is maintained in the aeration tank. By stirring,
Hydrolysis of ATP proceeds quickly and phosphorus is released, and under aerobic conditions due to subsequent aeration, ATP
is produced, allowing microorganisms to take in excess phosphorus, while under anaerobic conditions during the subsequent denitrification process, polyphosphate-accumulating microorganisms maintain normal respiratory metabolism due to the presence of nitrite or nitrate nitrogen. It was found that the ingested phosphorus is not released, and therefore the phosphorus content of the sludge is maintained at a high concentration through a series of biological treatment steps, and as a result, the phosphorus removal effect remains extremely high. It is something. In the present invention, a preferable method for keeping the redox potential of the raw wastewater to be treated below a certain value, that is, below -150mV, is to keep the raw wastewater to be treated in an anaerobic state for a certain period of time before injecting it into the aeration tank. It's a method. Such methods include maintaining an anaerobic state for a certain period of time in a storage tank before injecting the raw wastewater into the aeration tank, controlling aeration during mixing and stirring of the raw wastewater in the storage tank, or controlling the aeration while stirring the raw wastewater in the storage tank. It is preferable not to do so. Generally, by maintaining the anaerobic state for about one hour or more, the oxidation-reduction potential of raw wastewater is reduced to -
It can be 150mV or less. Such measurement of the redox potential of raw wastewater can be easily carried out using an ordinary redox potentiometer. In the present invention, wastewater that can be treated with nitrogen and phosphorus at the same time includes industrial wastewater including food factory wastewater, organic wastewater such as human waste and sewage, and wastewater that contains excessive amounts of nitrogen and phosphorus. If so, any wastewater can be treated. Especially when the BOD concentration is 100 mg/ to 5000 mg/
When wastewater has a BOD/nitrogen ratio of 3 or more, the treatment effect of the present invention is most significant. Such organic wastewater can usually be easily maintained in an anaerobic state unless it is kept in an oxidized state by aeration or the like. To give a specific example, when various amounts of wastewater from domestic sewage A, 20-fold diluted human waste digested liquid B, pharmaceutical factory C, and brewing factory D are aerated, the change in DO during aeration and the redox potential change. The relationship is as shown below, and therefore, by easily selecting the DO value in the waste water, the oxidation-reduction potential of the waste water can be easily controlled to -150 mV or less.

【表】 また、上記のA〜Dの排水を曝気によつてその
酸化還元電位を+100mVとし、その後曝気を停
止して撹拌のみを行つた場合、その酸化還元電位
の経時変化は第1図に示す如くである。従つて、
上記の如き排水の酸化還元電位は、いずれも曝気
停止後60分間程度で−150mV以下にすることが
できる。 本発明方法は以上の点を主たる特徴とし、それ
以外の生物学的処理工程は従来公知の工程でよ
い。上記の特徴を含有する本発明方法を本発明の
一実施態様を示す添付図面を参照して更に具体的
に説明すると、第2図に図解的に示す通り、処理
すべき原排水は、流入路1より貯留槽2に導か
れ、ここで一旦貯留される。この貯留槽中の原排
水は均質化の目的で撹拌混合するのが好ましい
が、前述の通り、この原排水の酸化還元電位を−
150mV以下に保持する必要があるため、混合撹
拌は機械的撹拌あるいは撹拌ポンプ等によつて行
うのが好ましく、曝気により撹拌混合する場合
は、原排水の酸化還元電位を監視しつつ、その酸
化還元電位が−150mV以上とならないように注
意する必要がある。またこの貯留槽の容量は、原
排水の滞留時間が常に1時間以上となる様に設定
することがよく、このようにすれば原排水の酸化
還元電位を−150mV以下に制御するのが更に容
易となる。 次いで貯留槽中の原排水は、原排水ポンプ3に
より、流入路4を経て曝気槽5に流入される。前
述の通り、本発明の第2の特徴は、この原排水の
曝気槽中への流入中は、曝気槽中で曝気を行わ
ず、そのまま撹拌混合、すなわち嫌気撹拌を行う
ことであり、この嫌気撹拌によつて原排水と活性
汚泥法とを十分に混合する。この嫌気撹拌によつ
て原排水中のATPが加水分解され十分な燐の放
出が生じる。このような嫌気撹拌は、撹拌ポンプ
等による機械的撹拌でもよいし、原排水の流入速
度を利用する撹拌方法のいずれでもよい。 原排水の流入が終了した後、曝気槽中で曝気を
開始する。曝気は、従来公知のいずれの方法でも
よく、例えば送風機7により管路8を経て送られ
る空気によつて行うことができる。この曝気工程
により流入した原排水中の窒素成分の硝化反応が
進行し、窒素成分の大部分は亜硝酸態あるいは硝
酸態の窒素に酸化される。このような窒素成分の
酸化が終了した時点で、曝気を終了させるのが好
ましく、従つて所定の曝気時間内に酸化が丁度完
了するように、負荷量、曝気量等を設定するのが
好ましい。また硝化反応は酸生成反応であるの
で、曝気中にPHが低下しすぎる場合にはアルカリ
剤を薬注路9から曝気槽中に添加するのが好まし
い。処理終了時の混合液のPHは通常は6.5〜9.5に
保持されていればよい。 硝化反応が終了し、曝気工程を終了した後は、
嫌気撹拌を行う。この嫌気撹拌は、薬注路10か
ら水素供与体を曝気槽中に添加するとともに曝気
槽内の撹拌ポンプ6により、曝気を行わずに曝気
撹拌を行い、脱窒反応を進行させ、窒素を窒素ガ
スとして分離させる。この嫌気工程で使用する水
素供与体としては、メタノール、エタノール、酢
酸、イソプロピルアルコール等の工業薬品、ある
いは流入排水組成に類似した窒素と燐を過剰に含
有しない廃液等が使用できる。この嫌気撹拌工程
における水素供与体の添加量は、硝化反応によつ
て生成した亜硝酸、硝酸態の窒素が脱窒反応によ
り、窒素ガスとして系外に除去されるに足る量で
十分である。また嫌気撹拌時間も脱窒反応が終了
するに必要な時間にする。 以上の脱窒反応が終了すると、添加した水素供
与体が消費されず、1部残存することがあるの
で、この水素供与体を除去するために短時間の再
曝気処理を行い、再曝気処理が終了後は撹拌を停
止して活性汚泥法を沈降分離させる沈澱工程に移
る。所定時間の沈澱工程が終了したら、放流路1
1によつて上澄水を処理済水として放流する。こ
の処理済水は、通常塩素または次亜塩素酸塩類等
の殺菌剤により減菌消毒処理するのが好ましい。 以上の処理で燐を過剰に摂取した余剰汚泥は、
鉢袋槽5からの処理済水の放流と同時に、あるい
はその前後に排泥管12から汚泥貯槽13に所定
量を排泥し、管路14から、脱水等の処理を行う
かまたはそのまま搬出して処分する。余剰汚泥の
脱水方法は、通常行われている脱水助剤としての
鉄塩を用いる方法で燐を汚泥中に有効に固定する
ことが可能であるため、特別な脱水方法は不要で
ある。 (作用・効果) 以上の如き本発明方法では、従来公知の比較的
低コストの回分式の排水処理設備をそのまま使用
して、排水の処理に際して原排水を嫌気状態に保
持し、特にその酸化還元電位を−150mV以下に
制御し、且つ原排水の曝気槽への流入中は、曝気
を行わずに嫌気撹拌を行うことによつて、ATP
の加水分解による燐の放出が有効に行われ、次い
で曝気による好気状態でATPが生産され、汚泥
が燐を効率的に過剰に摂取できる状態に保持され
ている。また脱窒反応の嫌気状態でも亜硝酸また
は硝酸態の窒素が存在するため、燐を過剰に摂取
した微生物は通常の呼吸代謝が行うことができ、
このような嫌気状態であつても、燐が放出されな
い。従つて本発明では従来の方法に比較して汚泥
の燐含有率を最後まで高く維持できるため、最後
に余剰汚泥を処分するのみで、燐を安定的且つ高
度に除去することができる。 また、本発明方法においては上記の燐の除去だ
けでなく、排水の流入工程における原排水の酸化
還元電位を−150mV以下の嫌気状態に保持して
も、生物学的な窒素の硝化処理および脱窒反応に
は何ら悪影響を及ぼさない。 従つて、本発明方法では、複雑で高価の設備を
要せずに、従来の回分式の設備をそのまま用い
て、排水中の窒素と燐を同時に効率的に処理して
分離することができる。 次に実施例を挙げて、本発明を更に具体的に説
明する。 実施例 1 曝気槽80のベンチスケール実験装置により、
グルコース180mg/、スターチ100mg/、ペプ
トン80mg/、燐酸2水素カリウム16mg/、尿
素50mg/、BOD250mg/、全窒素35mg/、
全燐6.5mg/を含む合成排水を用いて、曝気槽
へ流入する排水の酸化還元電位を変化させて実験
を行つた。実験の処理のタイムスケジユールは、
排水の流入1時間→曝気5時間→メタノール添加
0.25時間→嫌気撹拌3時間→再曝気1時間→沈澱
1時間→放流1時間であり、12時間で1回の処理
を完了させ、排水を半量入換えとして1日2サイ
クルで処理を行つた。 この実験では、曝気槽に流入する排水の酸化還
元電位を、貯留槽での曝気撹拌量を調整すること
により、+100mVから−300mVの範囲で変化させ
た処理効果を求めて比較した。 処理結果は、後記の第1表に示す通りであり、
BODおよび全窒素の処理効果は、流入する排水
の酸化還元電位に拘らず、一定であり、BOD10
mg/、全窒素10mg/以下となつている。一
方、全燐は、流入する排水の酸化還元電位が−
150mV以下に調整された時においてのみ、0.5
mg/以下の処理水質を示しており、排水の酸化
還元電位が−150mV以上の場合には、全燐は0.5
mg/以上であることを示しており、本発明の効
果が実証された。 実施例 2 処理能力2m3/日のパイロツトプラントにより
醤油製造工場排水の連続通水処理試験を実施し
た。この連続通水処理試験期間中の供試排水の性
状は、下記の通りであり、処理期間中のBOD、
窒素、燐の排水組成には大きな変化は観察され
ず、また、BOD:窒素:燐=100:12:1.5と窒
素と燐が過剰であることから、通常の活性汚泥法
による処理では、処理水中に窒素と燐とが残留す
る排水組成である。 σn−1 PH 7.0 0.2 SS(mg/) 230 114 TOC(mg/) 210 80 COD(mg/) 206 62 BOD(mg/) 606 183 全窒素(mg/) 70 18 全燐(mg/) 9.2 1.9 色度(度) 142 26 処理のタイムスケジユールは次の通りである。
すなわち、排水の1日分の貯留能力を有する貯留
槽から1時間で曝気槽へ排水を流入させた。貯留
槽では曝気による撹拌を行いつつ、酸化還元電位
計により−150mVの嫌気状態を流入工程で常に
保つ様に制御した。排水流入工程では嫌気撹拌を
行い、流入終了後、曝気を開始した。曝気による
硝化工程を12時間とし、硝化工程が終了したら、
水素供与体としてイソプロピルアルコールを添加
し、嫌気撹拌工程による脱窒処理を6時間行う。
脱窒処理終了後、再曝気工程2時間、沈澱工程2
時間、処理水の放流1時間とし、1回の処理が24
時間で完了するスケジユールである。 上記の処理結果は、第3図に示す通りで、処理
期間中のBOD成分Aの除去率は、98〜99%であ
り、最大でも20mg/を越えることがなかつた。
窒素成分Bについても除去率は93〜98%であり、
最大でも10mg/を越えることがなかつた。また
燐成分Cについても除去率は97〜98%であり、最
大でも0.5mg/を越えることがなかつた。 以上の結果から、本発明方法による生物学的処
理による窒素と燐の同時処理方法は、極めて安定
した処理効果を発揮することが明らかである。 比較例 1 実施例2において、貯留槽では曝気による撹拌
を行い、酸化還元電位計により、排水の酸化還元
電位を常に−150mV以上に制御したことを除い
て、他は実施例2と全く同様にして処理を行つ
た。結果は第4図に示す通りである。 第4図に示す如く、処理期間中のBOD成分
A′の除去率は98〜99%、窒素成分B′の除去率は
93〜95%であり、実施例と比較して有意差は認め
られなかつたが、燐成分C′の除去率は45〜97%で
あり、燐成分の除去に関しては処理効果の安定を
図ることは困難であつた。 以上のことから排水の酸化還元電位が−
150mV以上では、本発明の目的が達成できない
ことが明らかである。
[Table] In addition, when the above wastewater A to D is aerated to bring its redox potential to +100 mV, and then the aeration is stopped and only stirring is performed, the change in redox potential over time is shown in Figure 1. As shown. Therefore,
The oxidation-reduction potential of the waste water as described above can be reduced to -150 mV or less within about 60 minutes after stopping the aeration. The method of the present invention has the above-mentioned main features, and the other biological treatment steps may be conventionally known steps. The method of the present invention having the above characteristics will be explained in more detail with reference to the accompanying drawings showing one embodiment of the present invention.As schematically shown in FIG. 1 to a storage tank 2, where it is temporarily stored. It is preferable to stir and mix the raw wastewater in this storage tank for the purpose of homogenization, but as mentioned above, the oxidation-reduction potential of this raw wastewater is -
Since it is necessary to maintain the voltage below 150 mV, it is preferable to perform mixing and stirring using mechanical stirring or a stirring pump. When stirring and mixing by aeration, the redox potential of the raw wastewater is monitored and the redox potential of the raw wastewater is monitored. Care must be taken to ensure that the potential does not exceed -150mV. In addition, the capacity of this storage tank is preferably set so that the residence time of the raw wastewater is always at least 1 hour, and in this way, it is easier to control the redox potential of the raw wastewater to -150 mV or less. becomes. Next, the raw wastewater in the storage tank is caused to flow into the aeration tank 5 via the inflow path 4 by the raw wastewater pump 3 . As mentioned above, the second feature of the present invention is that while this raw wastewater is flowing into the aeration tank, aeration is not performed in the aeration tank, and stirring and mixing, that is, anaerobic stirring, is performed as it is, and this anaerobic Thoroughly mix raw wastewater and activated sludge method by stirring. This anaerobic agitation hydrolyzes ATP in the raw wastewater and releases sufficient phosphorus. Such anaerobic stirring may be performed by mechanical stirring using a stirring pump or the like, or by any stirring method that utilizes the inflow velocity of raw wastewater. After the raw wastewater has finished flowing in, aeration begins in the aeration tank. Aeration may be carried out by any conventionally known method, for example by air sent through pipe 8 by blower 7. Through this aeration process, the nitrification reaction of the nitrogen components in the raw wastewater flowing in progresses, and most of the nitrogen components are oxidized to nitrite or nitrate nitrogen. It is preferable to terminate the aeration when the oxidation of the nitrogen component is completed, and therefore it is preferable to set the load amount, aeration amount, etc. so that the oxidation is exactly completed within a predetermined aeration time. Further, since the nitrification reaction is an acid production reaction, it is preferable to add an alkaline agent into the aeration tank through the chemical injection path 9 if the pH drops too much during aeration. The pH of the mixed solution at the end of the treatment should normally be maintained at 6.5 to 9.5. After the nitrification reaction is completed and the aeration process is completed,
Perform anaerobic stirring. In this anaerobic stirring, a hydrogen donor is added into the aeration tank from the chemical injection path 10, and the stirring pump 6 in the aeration tank performs aeration stirring without aeration to advance the denitrification reaction and convert nitrogen into nitrogen. Separate it as a gas. As the hydrogen donor used in this anaerobic process, industrial chemicals such as methanol, ethanol, acetic acid, isopropyl alcohol, etc., or waste liquids having a composition similar to the influent wastewater but not containing excessive amounts of nitrogen and phosphorus, etc. can be used. The amount of hydrogen donor added in this anaerobic stirring step is sufficient to remove nitrogen in the form of nitrite and nitrate produced by the nitrification reaction from the system as nitrogen gas by the denitrification reaction. Also, the anaerobic stirring time is set to be the time required to complete the denitrification reaction. When the above denitrification reaction is completed, the added hydrogen donor is not consumed and some portion may remain, so a short reaeration process is performed to remove this hydrogen donor. After the completion of the process, the stirring is stopped and the activated sludge method moves to the sedimentation step where the activated sludge method is separated by sedimentation. After the settling process for a predetermined period of time is completed, the discharge channel 1
1, the supernatant water is discharged as treated water. This treated water is usually preferably sterilized and disinfected using a disinfectant such as chlorine or hypochlorites. Surplus sludge that has taken in excessive phosphorus through the above treatment is
Simultaneously with or before or after discharging the treated water from the pot bag tank 5, a predetermined amount of sludge is removed from the sludge pipe 12 into the sludge storage tank 13, and either subjected to treatment such as dewatering from the pipe 14, or carried out as is. Dispose of it. As for the dewatering method of excess sludge, phosphorus can be effectively fixed in the sludge by a commonly used method using iron salt as a dewatering aid, so no special dewatering method is necessary. (Function/Effect) In the method of the present invention as described above, conventionally known comparatively low-cost batch-type wastewater treatment equipment is used as is, raw wastewater is maintained in an anaerobic state during wastewater treatment, and in particular, the oxidation and reduction ATP
The hydrolysis of phosphorus effectively releases phosphorus, and then ATP is produced under aerobic conditions through aeration, and the sludge is maintained in a state where it can efficiently uptake phosphorus in excess. In addition, even in the anaerobic state of denitrification reactions, nitrite or nitrate nitrogen is present, so microorganisms that have ingested too much phosphorus can carry out normal respiratory metabolism.
Even under such anaerobic conditions, phosphorus is not released. Therefore, in the present invention, the phosphorus content of the sludge can be maintained higher until the end compared to the conventional method, so that phosphorus can be removed stably and to a high degree by simply disposing of the excess sludge at the end. In addition, the method of the present invention not only removes phosphorus as described above, but also maintains the redox potential of raw wastewater in an anaerobic state of -150 mV or less during the wastewater inflow process. It does not have any adverse effect on the nitrogen reaction. Therefore, in the method of the present invention, nitrogen and phosphorus in wastewater can be efficiently treated and separated simultaneously using conventional batch-type equipment without requiring complicated and expensive equipment. Next, the present invention will be explained in more detail with reference to Examples. Example 1 Using a bench scale experimental device with an aeration tank of 80,
Glucose 180mg/, Starch 100mg/, Peptone 80mg/, Potassium dihydrogen phosphate 16mg/, Urea 50mg/, BOD 250mg/, Total nitrogen 35mg/,
Experiments were conducted using synthetic wastewater containing 6.5 mg of total phosphorus and varying the redox potential of the wastewater flowing into the aeration tank. The time schedule for processing the experiment is
Inflow of wastewater for 1 hour → Aeration for 5 hours → Addition of methanol
The process was as follows: 0.25 hours → 3 hours of anaerobic stirring → 1 hour of re-aeration → 1 hour of precipitation → 1 hour of discharge, one treatment was completed in 12 hours, and half of the wastewater was replaced, and the treatment was performed in two cycles a day. In this experiment, we determined and compared the treatment effects of changing the redox potential of wastewater flowing into the aeration tank in the range of +100mV to -300mV by adjusting the amount of aeration stirring in the storage tank. The processing results are as shown in Table 1 below,
The treatment effect of BOD and total nitrogen is constant regardless of the redox potential of the inflowing wastewater, and BOD10
mg/, total nitrogen is less than 10 mg/. On the other hand, total phosphorus has a redox potential of -
0.5 only when adjusted below 150mV
mg/or less, and if the redox potential of the wastewater is -150mV or more, the total phosphorus is 0.5
mg/ or more, demonstrating the effectiveness of the present invention. Example 2 A continuous water flow treatment test for soy sauce manufacturing factory wastewater was carried out using a pilot plant with a treatment capacity of 2 m 3 /day. The properties of the sample wastewater during this continuous water flow treatment test period are as follows: BOD during the treatment period,
No major changes were observed in the composition of nitrogen and phosphorus in the wastewater, and since nitrogen and phosphorus were excessive (BOD: nitrogen: phosphorus = 100:12:1.5), treatment using the normal activated sludge method The composition of the wastewater is such that nitrogen and phosphorus remain in the wastewater. x σn−1 PH 7.0 0.2 SS (mg/) 230 114 TOC (mg/) 210 80 COD (mg/) 206 62 BOD (mg/) 606 183 Total nitrogen (mg/) 70 18 Total phosphorus (mg/) 9.2 1.9 Chromaticity (degrees) 142 26 The processing time schedule is as follows.
That is, wastewater was allowed to flow into the aeration tank in one hour from a storage tank that had a storage capacity for one day's worth of wastewater. The storage tank was stirred by aeration and controlled using an oxidation-reduction potentiometer to constantly maintain an anaerobic state of -150 mV during the inflow process. Anaerobic stirring was performed during the wastewater inflow process, and aeration was started after the inflow was completed. The nitrification process by aeration is for 12 hours, and once the nitrification process is finished,
Isopropyl alcohol is added as a hydrogen donor, and denitrification treatment is performed by an anaerobic stirring process for 6 hours.
After the denitrification process, 2 hours of re-aeration process, precipitation process 2
The treated water is discharged for 1 hour, and one treatment takes 24 hours.
It is a schedule that can be completed within a certain amount of time. The results of the above treatment are as shown in FIG. 3, and the removal rate of BOD component A during the treatment period was 98 to 99%, and did not exceed 20 mg/at maximum.
The removal rate for nitrogen component B is also 93-98%.
The maximum dose never exceeded 10mg/. In addition, the removal rate of phosphorus component C was 97 to 98%, and the amount did not exceed 0.5 mg/at maximum. From the above results, it is clear that the method of simultaneously treating nitrogen and phosphorus by biological treatment according to the method of the present invention exhibits an extremely stable treatment effect. Comparative Example 1 In Example 2, everything else was the same as in Example 2, except that the storage tank was agitated by aeration and the redox potential of the wastewater was always controlled to -150 mV or higher using a redox potentiometer. I processed it. The results are shown in FIG. As shown in Figure 4, BOD components during the treatment period
The removal rate of A′ is 98-99%, and the removal rate of nitrogen component B′ is
Although the removal rate of phosphorus component C' was 45 to 97%, it was necessary to stabilize the treatment effect regarding the removal of phosphorus component. was difficult. From the above, the oxidation-reduction potential of wastewater is -
It is clear that the object of the present invention cannot be achieved at 150 mV or more.

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

第1図は、嫌気撹拌による各種排水の酸化還元
電位の経時変化を示し、第2図は、本発明の処理
工程を図解的に示すものであり、第3図は、本発
明の実施例2による排水中のBOD(mg/)、全
窒素(mg/)および全燐(mg/)の除去効果
を示し、第4図は、比較例による同上の除去効果
を示している。 1……流入路、2……貯留槽、3……ポンプ、
4……流路、5……曝気槽、6……撹拌ポンプ、
7……送風機、8……管路、9……薬注路、10
……薬注路、11……放流路、12……排泥管、
13……汚泥貯槽、14……管路、A……BOD
(mg/)、B……全窒素(mg/)、C……全燐
(mg/)、A′……BOD(mg/)、B′……全窒素
(mg/)、C′……全燐(mg/)。
FIG. 1 shows changes over time in the oxidation-reduction potential of various wastewaters caused by anaerobic stirring, FIG. 2 schematically shows the treatment process of the present invention, and FIG. 3 shows Example 2 of the present invention. Fig. 4 shows the removal effect of BOD (mg/), total nitrogen (mg/), and total phosphorus (mg/) in wastewater in wastewater by the method, and Fig. 4 shows the removal effect of the above by a comparative example. 1...Inflow path, 2...Storage tank, 3...Pump,
4... Channel, 5... Aeration tank, 6... Stirring pump,
7...Blower, 8...Pipeline, 9...Medicine injection channel, 10
...Medical injection channel, 11...Discharge channel, 12...Sludge drainage pipe,
13...Sludge storage tank, 14...Pipe line, A...BOD
(mg/), B...Total nitrogen (mg/), C...Total phosphorus (mg/), A'...BOD (mg/), B'...Total nitrogen (mg/), C'... Total phosphorus (mg/).

Claims (1)

【特許請求の範囲】[Claims] 1 嫌気工程および好気工程を含む回分式の活性
汚泥法による排水の生物学的処理方法において、
曝気槽へ導入する排水を嫌気性貯留槽中に1時間
以上滞留させて酸化還元電位を−150mV以下に
制御した後、該排水を曝気槽に導入し、且つ曝気
槽中への排水の流入中は嫌気撹拌を行い、排水か
ら窒素および燐を同時に除去することを特徴とす
る排水の生物学的処理方法。
1. In a biological treatment method for wastewater using a batch activated sludge method including an anaerobic process and an aerobic process,
After the wastewater to be introduced into the aeration tank is allowed to stay in the anaerobic storage tank for at least one hour and the redox potential is controlled to -150mV or less, the wastewater is introduced into the aeration tank, and while the wastewater is flowing into the aeration tank. is a biological treatment method for wastewater that is characterized by the simultaneous removal of nitrogen and phosphorus from wastewater through anaerobic agitation.
JP23754084A 1984-11-13 1984-11-13 Biological treatment of waste water Granted JPS61118195A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23754084A JPS61118195A (en) 1984-11-13 1984-11-13 Biological treatment of waste water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23754084A JPS61118195A (en) 1984-11-13 1984-11-13 Biological treatment of waste water

Publications (2)

Publication Number Publication Date
JPS61118195A JPS61118195A (en) 1986-06-05
JPH0476757B2 true JPH0476757B2 (en) 1992-12-04

Family

ID=17016843

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23754084A Granted JPS61118195A (en) 1984-11-13 1984-11-13 Biological treatment of waste water

Country Status (1)

Country Link
JP (1) JPS61118195A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63126599A (en) * 1986-11-17 1988-05-30 Nippon Steel Corp Biochemical treatment of waste water
ES2127014T3 (en) * 1995-05-11 1999-04-01 Biobalance As NEW METHOD TO CONTROL BIODEGRADATION.

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5757195A (en) * 1980-09-25 1982-04-06 Tadano Tekkosho Kk Preventive device for overload of crane
JPS57150485A (en) * 1981-03-13 1982-09-17 Nippon Kentetsu Co Ltd Batch-wise activated sludge treatment device
JPS58210897A (en) * 1982-06-02 1983-12-08 Hitachi Plant Eng & Constr Co Ltd Biological dephosphorization method of waste water
JPS5980399A (en) * 1982-10-27 1984-05-09 Hitachi Ltd Control device for biological denitrification treatment equipment
JPS5995997A (en) * 1982-11-22 1984-06-02 Hitachi Plant Eng & Constr Co Ltd Biological dephosphorization method of wastewater
JPS59136193A (en) * 1983-01-25 1984-08-04 Sumitomo Jukikai Envirotec Kk Biological dephosphorizing method of waste water

Also Published As

Publication number Publication date
JPS61118195A (en) 1986-06-05

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