JPS6345639B2 - - Google Patents

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Publication number
JPS6345639B2
JPS6345639B2 JP59246122A JP24612284A JPS6345639B2 JP S6345639 B2 JPS6345639 B2 JP S6345639B2 JP 59246122 A JP59246122 A JP 59246122A JP 24612284 A JP24612284 A JP 24612284A JP S6345639 B2 JPS6345639 B2 JP S6345639B2
Authority
JP
Japan
Prior art keywords
sludge
tank
liquid
mixing
phosphorus
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
JP59246122A
Other languages
Japanese (ja)
Other versions
JPS61125489A (en
Inventor
Toshihiro Tanaka
Yoshiro Hayashi
Akira Kawakami
Yutaka Yoneyama
Itsuhito Ikebukuro
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
Original Assignee
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 Infilco Co Ltd filed Critical Ebara Infilco Co Ltd
Priority to JP59246122A priority Critical patent/JPS61125489A/en
Publication of JPS61125489A publication Critical patent/JPS61125489A/en
Publication of JPS6345639B2 publication Critical patent/JPS6345639B2/ja
Granted legal-status Critical Current

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  • Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
  • Treatment Of Sludge (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、家庭下水ないし、産業廃液、それに
類する有機性廃液などの有機物とリンを含む廃液
の処理法に関するもので、特に嫌気−好気活性汚
泥法と言われる生物脱リン技術の改良に関するも
のである。 〔従来技術〕 一般に、生物処理工程である嫌気−好気活性汚
泥法とは、従来の活性汚泥法施設における曝気槽
の被処理流入端を溶存酸素(DO)も硝酸根ある
いは亜硝酸根(NO)も実質的に存在しない嫌
気状態の帯域(以下これを嫌気槽という)にし、
ここで被処理液と返送汚泥を混合し、しかるのち
にこの混合液を後段の曝気された帯域(以下これ
を好気槽という)に導いて曝気処理し、さらに沈
殿池で固液分離をはかる技術である。 具体的には、第3図に示すように、家庭下水な
どの有機性廃液である被処理液1は、最初沈殿池
2にて最初沈殿池汚泥3を分離し、その上澄液4
は最終沈殿池11にて分離され返送された最終沈
殿池汚泥13と共に嫌気槽5へ導入され、撹拌機
6で混合されながら嫌気処理される。ここで活性
汚泥はリンを放出すると共に被処理液中のBOD
の一部を摂取する。次いで、この嫌気槽流出混合
液7は好気槽8に導かれ、散気器9による曝気に
より残留BOD成分その他の有機物が酸化分解さ
れると同時に液中の溶解性リンが活性汚泥中に摂
取され、かくて好気槽8においてBODと溶解性
リンが減少した好気槽流出混合液10は、最終沈
殿池11に送られて処理液12と最終沈殿池汚泥
13に分離される。この最終沈殿池汚泥13は、
一部返送汚泥として嫌気槽5に返送されるが、残
部は余剰汚泥14として、最初沈殿池2に移送さ
れ、最初沈殿池汚泥3などと共に初沈汚泥濃縮槽
15で濃縮され、初沈汚泥濃縮槽上澄液16は被
処理液1と共に処理され、濃縮初沈汚泥17は脱
水助剤などが添加され脱水機18等によつて処理
され、分離液19は被処理液1に混入される。 このような特徴のある嫌気−好気活性汚泥法の
工程構成では、標準活性汚泥法で生成される活性
汚泥よりもリン摂取能力の高い活性汚泥が生成さ
れ、BOD、SSなどの汚濁物の除去と同時に被処
理液中に存在する溶解性リンの大部分を活性汚泥
に吸収せしめることができる。 〔発明が解決しようとする問題点〕 このような嫌気−好気活性汚泥法で生成される
活性汚泥(最終沈殿池汚泥13)は、標準的な活
性汚泥法で生成される汚泥よりもリン含有率が高
く、嫌気状態におかれた場合には汚泥中からリン
が再放出され、余剰汚泥の汚泥処理工程で生ずる
分離液中に高濃度のリンが含有されることにな
る。したがつて、この分離液の処理も必要とな
り、該処理系の流入端などに返送され、被処理液
とともに処理される。しかしながら、この分離液
を返送することは該処理系の流入リン負荷量の増
大を来たし、嫌気−好気活性汚泥法におけるリン
除去性能を低下させたり、不安定なものにするの
でこの分離液中のリン濃度をできるだけ減少させ
ることが必要であつた。 また、従来嫌気−好気活性汚泥法から発生する
汚泥の処理においては、余剰汚泥は最初沈殿池に
移送され、系内で発生する汚泥は全量最初沈殿池
を経由して濃縮され、その後に脱水処理されてい
た。 しかしこの方法では、最初沈殿池に流入する被
処理液のBOD濃度が高いが、最初沈殿池に移送
された余剰汚泥中の大部分のポリリン(60〜80
%)が液中に放出され、液中のP/BOD比は、
0.06以上となるため嫌気−好気活性汚泥法の最終
処理液中に高濃度のリンが残留するようになり、
生物学的リンの除去は実質的に行われなくなる欠
点があつた。 本発明は、これら従来の嫌気−好気活性汚泥法
の問題点を排除し、処理系のリン負荷量の増大を
防止し、リン除去を常に安定して行わしめる方法
を提供することを目的とするものである。 〔問題点を解決するための手段〕 本願発明は、被処理液を最初沈殿池で沈殿分離
し、該分離液と返送汚泥とを、溶存酸素、硝酸、
亜硝酸のいずれもが実質的に存在しない嫌気状態
で混合処理したのち、曝気処理を行い、該曝気混
合液を最終沈殿池で沈殿分離し、該沈殿汚泥の一
部を前記返送汚泥とし、残部を余剰汚泥とする有
機性廃液の生物学的処理方法において、最初沈殿
池汚泥と最終沈殿池からの前記余剰汚泥をそれぞ
れ別個に濃縮し、これら両方の濃縮汚泥を混合す
ると同時に又は混合直後に鉄塩化合物を鉄として
汚泥固形物当り1〜5%添加し、かつそのPHが6
〜8になるように消石灰を添加混合処理したの
ち、脱水処理を行うことを特徴とする有機性廃液
の処理方法である。 〔作用〕 本発明の実施態様を図面に基づいて説明する
と、第1図示例において、家庭下水などの有機性
廃液である被処理液1は最初沈殿池2で最初沈殿
池汚泥3を分離し、該上澄液4は最終沈殿池11
から返送される最終沈殿池汚泥13と共に嫌気槽
5に導入され撹拌機6で混合されて嫌気処理され
る。活性汚泥は、ここでその細胞内に貯留した高
分子リン化合物(ポリリン)を加水分解し溶液側
に放出するとともに、この際に得られるエネルギ
ーを利用して、被処理液に含まれるBODの一部
を細胞内に摂取し、細胞内貯留有機物とする。こ
の嫌気処理の反応を行わしめる嫌気槽5の規模は
流入する最初沈殿池2の上澄液4の組成や濃度に
よつて異なるが、家庭下水を被処理液とした場合
には、被処理液流入量として0.5〜2.5時間分でよ
い。 このようにして、溶解性リンが増加し、BOD
が減少した嫌気槽流出混合液7は、連設又は連通
状態下に区画された好気槽8に導かれる。この好
気槽8は空気その他の酸素含有性気体を散気器9
から給気して曝気されており、嫌気槽流出混合液
7に含まれる活性汚泥は嫌気槽5で摂取しきれな
かつたBOD成分を摂取し、酸化分解するととも
に細胞内貯留有機物も酸化分離される。また、該
活性汚泥は、この有機物の酸化状謝の際に生成さ
れるエネルギーの一部を利用して、細胞外に存在
する溶解性リンを細胞内に摂取しつつ細胞内に高
分子リン化合物(ポリリン)を含成する。この際
に嫌気槽5で放出された以上の量の溶解性リンが
摂取され、混合液中の溶解性リン濃度は被処理液
1のそれよりも低くなる。完全な溶解性リン除去
を行うためには、被処理液のP/BOD比が日間
平均値で0.06以下であることが必要であるが、家
庭下水の多くはその条件を満たす。この場合、
BODの酸化分解と溶解性リン除去を完遂せしめ
るためには、好嫌気8のBOD汚泥負荷F/M比
を0.05〜0.7(1/日)、好ましくは0.3〜0.5(1/
日)の範囲に制御する必要がある。 かくして好気槽8で生成され、BODと溶解性
リンが減少した好気槽流出混合液10は最終沈殿
池11に送られ、処理液12と最終沈殿池汚泥1
3に固液分離される。この最終沈殿池汚泥13の
一部は返送汚泥として嫌気槽5に返送され、残部
は余剰汚泥14として余剰汚泥濃縮槽20に移送
され、余剰汚泥濃縮槽上澄液21と濃縮余剰汚泥
22に分離される。また、最初沈殿池2で分離さ
れた最初沈殿池汚泥3は初沈汚泥濃縮槽15で濃
縮される。これら汚泥の濃縮度は両者共にそれぞ
れ汚泥濃度が1%以上となるように濃縮すること
が好ましい。 次に濃縮初沈汚泥17と濃縮余剰汚泥22は混
合槽23で混合される。両濃縮汚泥を混合すると
濃縮余剰汚泥22中のリンが短時間のうちに多量
に放出されるので、リン放出を防止するために鉄
塩化合物24を添加混合すると共に、該混合時の
PHが6〜8になるように消石灰25を添加する。 鉄塩化合物24の添加量は汚泥の性状によつて
異なるが、汚泥の固形物当り鉄として1〜5%混
合することが必要であり、また鉄塩化合物24と
消石灰25の添加混合は、両濃縮汚泥の混合と同
時に開始することが好ましいが、混合後1時間以
内であればリン固定の効果の差は小さいので、こ
の時間内であればよい。鉄塩化合物24と消石灰
25の混合方法は混合槽23で混合するだけでな
く、混合槽濃縮汚泥26の移送ラインに混合器を
設けて濃縮汚泥と混合させてもよい。鉄塩化合物
24としては、塩化第一鉄、塩化第二鉄、硫酸第
一鉄の使用が好ましい。また、PH6〜8となるよ
うに消石灰25の添加量を調整するには、消石灰
注入ポンプ27をPH計28で制御すればよい。 次に、この鉄塩化合物24と消石灰25を混合
された混合槽濃縮汚泥26は脱水機18に導入さ
れて脱水され、脱水ケーキ29として取り出され
る。混合槽濃縮汚泥26を脱水する際、汚泥を長
時間放置すると汚泥からリンが再放出するため、
鉄塩化合物24と消石灰25を添加混合後5時間
以内に脱水すれば、分離液19中のリン濃度を低
下させることができるので、効果的である。 使用する脱水機18としては、ベルトプレス脱
水機、遠心脱水機等の通常の脱水機が使用でき
る。脱水ケーキ29は通常乾燥、焼却等で処分さ
れる。 なお、脱水機18から流出する分離液19は返
送され被処理液1又は最初沈殿池2の上澄液4と
混合処理される。分離液19中のリン濃度は低く
なつており、この分離液19を返送し被処理液1
と混合しても流入リン負荷量の増大をきたすこと
はない。 第2図示例は、第1図示例と基本的には同様で
あるが嫌気槽5と好気槽8の間に脱窒素槽30を
設け、嫌気槽5の嫌気槽流出混合液7と、、好気
槽流出混合液10の一部を脱窒素槽30に導入
し、混合撹拌することにより、液中に含まれる
NOxが脱窒されるとともに、嫌気槽流出混合液
7に含まれる溶解性リンの一部が汚泥中に吸収さ
れる。このため第2図示例においては、原水中の
BOD、リン除去だけでなく、窒素除去も可能と
なる。 以上述べたように本発明においては、嫌気−好
気活性汚泥法の前段の最初沈殿池汚泥と嫌気−好
気活性汚泥法で発生する余剰汚泥とを別々に分離
して濃縮したのち、濃縮初沈汚泥と濃縮余剰汚泥
を混合すると同時又は直後に鉄塩化合物を該混合
汚泥の固形物当り鉄として1〜5%の範囲で混合
すると共に、混合時のPHが6〜8になるように消
石灰を混合したのち脱水処理を行うことにより、
脱水時の分離液中のリン濃度を低下させ、これら
汚泥処理系からのリンの返送量を軽減し、嫌気−
好気活性汚泥法の水処理系のリン負荷量増大を防
止し、リン除去を常に安定して処理できるもので
ある。 〔実施例〕 次に本発明の実施例を示す。 実施例 1 住宅団地より排出された家庭下水を被処理液と
して、第1図示例の方法で処理した。それぞれの
装置仕様は次の通りであつた。 最初沈殿池2:円形クラリフアリヤ 水容積 4
m3 嫌気槽5:2連式円筒撹拌槽 水容積 4m3 好気槽8:4画室化矩形槽 水容積 7m3 最終沈殿池11:円形クラリフアイヤ 水容積
7m3 初沈汚泥濃縮槽(重力式)15:円形クラリフア
イヤ 水容積 0.6m3 水面積 0.15m2 余剰汚泥濃縮槽(重力式)20:円形クラリフア
イヤ 水容積 0.6m3 水面積 0.3m2 脱水機18:遠心分離機 処理量 10Kg/h このような施設を用いて、被処理液1量55m3
d返送汚泥13流量15.4m3/dで処理したとこ
ろ、表−1に示すような処理液が得られた。
[Field of Industrial Application] The present invention relates to a method for treating wastewater containing organic matter and phosphorus, such as domestic sewage, industrial wastewater, and similar organic wastewater. This is related to the improvement of dephosphorization technology. [Prior art] In general, the anaerobic-aerobic activated sludge method, which is a biological treatment process, is a biological treatment process in which dissolved oxygen (DO), nitrate radicals, or nitrite radicals (NO ) in an anaerobic state (hereinafter referred to as an anaerobic tank),
Here, the liquid to be treated and the returned sludge are mixed, and then this mixed liquid is led to the aerated zone in the latter stage (hereinafter referred to as the aerobic tank) for aeration treatment, and then solid-liquid separation is performed in the settling tank. It's technology. Specifically, as shown in FIG. 3, the liquid to be treated 1, which is an organic waste liquid such as domestic sewage, is separated from the primary sedimentation tank sludge 3 in the primary sedimentation tank 2, and the supernatant liquid 4 is
is introduced into the anaerobic tank 5 together with the final sedimentation tank sludge 13 that has been separated and returned in the final sedimentation tank 11, and is subjected to anaerobic treatment while being mixed by the stirrer 6. Here, activated sludge releases phosphorus and BOD in the liquid to be treated.
ingest a portion of Next, this anaerobic tank effluent mixed liquid 7 is led to an aerobic tank 8, where residual BOD components and other organic matter are oxidized and decomposed by aeration by an aerator 9, and at the same time, soluble phosphorus in the liquid is absorbed into activated sludge. The aerobic tank effluent mixed liquid 10 in which BOD and soluble phosphorus have been reduced in the aerobic tank 8 is sent to the final settling tank 11 and separated into a treated liquid 12 and a final settling tank sludge 13. This final settling tank sludge 13 is
A portion is returned to the anaerobic tank 5 as returned sludge, but the remainder is transferred to the initial settling tank 2 as surplus sludge 14, and concentrated in the initial settling sludge thickening tank 15 together with the initial settling tank sludge 3, etc., to concentrate the initial settling sludge. The tank supernatant liquid 16 is treated together with the liquid to be treated 1, the concentrated initial settling sludge 17 is treated with a dehydrator 18 etc. to which a dewatering aid is added, and the separated liquid 19 is mixed into the liquid to be treated 1. The process structure of the anaerobic-aerobic activated sludge method, which has these characteristics, produces activated sludge with a higher phosphorus uptake capacity than the activated sludge produced by the standard activated sludge method, making it easier to remove pollutants such as BOD and SS. At the same time, most of the soluble phosphorus present in the liquid to be treated can be absorbed into the activated sludge. [Problems to be solved by the invention] The activated sludge (final settling tank sludge 13) produced by such an anaerobic-aerobic activated sludge method has a higher phosphorus content than the sludge produced by the standard activated sludge method. If the rate is high and the sludge is placed in an anaerobic state, phosphorus will be re-released from the sludge, resulting in a high concentration of phosphorus being contained in the separated liquid produced in the sludge treatment process for excess sludge. Therefore, this separated liquid also needs to be treated, and is returned to the inlet end of the treatment system and treated together with the liquid to be treated. However, returning this separated liquid increases the amount of phosphorus that flows into the treatment system, lowers the phosphorus removal performance in the anaerobic-aerobic activated sludge process, and makes it unstable. It was necessary to reduce the phosphorus concentration of In addition, in the treatment of sludge generated from the conventional anaerobic-aerobic activated sludge method, excess sludge is transferred to the initial settling tank, and all of the sludge generated in the system is concentrated via the initial settling tank, and then dewatered. It was being processed. However, with this method, although the BOD concentration of the liquid to be treated flowing into the first settling tank is high, most of the polyphosphorus (60 to 80%) in the excess sludge transferred to the first settling tank is
%) is released into the liquid, and the P/BOD ratio in the liquid is:
0.06 or higher, a high concentration of phosphorus will remain in the final treatment liquid of the anaerobic-aerobic activated sludge method.
The disadvantage was that biological phosphorus removal was virtually impossible. The purpose of the present invention is to provide a method that eliminates these problems of the conventional anaerobic-aerobic activated sludge method, prevents an increase in the phosphorus load in the treatment system, and always performs stable phosphorus removal. It is something to do. [Means for Solving the Problems] The present invention first performs sedimentation separation on the liquid to be treated in a settling tank, and then separates the separated liquid and returned sludge into dissolved oxygen, nitric acid,
After mixing in an anaerobic state in which nitrous acid is not substantially present, aeration treatment is performed, and the aerated mixture is separated by sedimentation in a final settling tank, a part of the settled sludge is used as the return sludge, and the remainder is In a biological treatment method for organic wastewater that uses surplus sludge, the surplus sludge from the initial settling tank and the final settling tank are concentrated separately, and both thickened sludges are mixed at the same time or immediately after mixing. A salt compound is added as iron in an amount of 1 to 5% per sludge solid, and its pH is 6.
This is a method for treating organic waste liquid, which is characterized in that slaked lime is added and mixed to a concentration of ~8, and then dehydrated. [Function] To explain the embodiment of the present invention based on the drawings, in the first illustrated example, the liquid to be treated 1, which is an organic waste liquid such as domestic sewage, is separated from the first sedimentation tank sludge 3 in the first sedimentation tank 2, The supernatant liquid 4 is sent to the final settling tank 11.
The sludge is introduced into the anaerobic tank 5 together with the final settling tank sludge 13 returned from the sludge, mixed by the stirrer 6, and subjected to anaerobic treatment. Activated sludge hydrolyzes the high molecular phosphorus compound (polyphosphorus) stored in its cells and releases it into the solution, and uses the energy obtained at this time to remove some of the BOD contained in the liquid to be treated. is taken into cells and used as intracellularly stored organic matter. The scale of the anaerobic tank 5 that performs this anaerobic treatment reaction varies depending on the composition and concentration of the supernatant liquid 4 of the initial settling tank 2 flowing into it, but when domestic sewage is used as the liquid to be treated, The inflow amount may be 0.5 to 2.5 hours. In this way, soluble phosphorus increases and BOD
The anaerobic tank effluent mixed liquid 7 in which the anaerobic tank has been reduced is led to an aerobic tank 8 which is partitioned in a continuous or communicating state. This aerobic tank 8 supplies air and other oxygen-containing gases to an aeration chamber 9.
The activated sludge contained in the anaerobic tank outflow mixed liquid 7 takes in the BOD components that could not be taken up in the anaerobic tank 5 and is oxidized and decomposed, and the organic matter stored in the cells is also oxidized and separated. . In addition, the activated sludge utilizes part of the energy generated during the oxidation of organic matter to absorb soluble phosphorus that exists outside the cells into the cells, while also ingesting polymeric phosphorus compounds into the cells. Contains (polyline). At this time, an amount of soluble phosphorus greater than that released in the anaerobic tank 5 is ingested, and the soluble phosphorus concentration in the mixed liquid becomes lower than that in the liquid to be treated 1. In order to completely remove soluble phosphorus, the daily average P/BOD ratio of the liquid to be treated must be 0.06 or less, and most domestic sewage satisfies this condition. in this case,
In order to complete the oxidative decomposition of BOD and the removal of soluble phosphorus, the BOD sludge loading F/M ratio of aerobic and anaerobic 8 should be adjusted to 0.05 to 0.7 (1/day), preferably 0.3 to 0.5 (1/day).
day). The aerobic tank effluent mixed liquid 10 generated in the aerobic tank 8 and reduced in BOD and soluble phosphorus is sent to the final settling tank 11, where it is mixed with the treated liquid 12 and the final settling tank sludge 1.
Solid-liquid separation is carried out in 3 steps. A part of this final settling tank sludge 13 is returned to the anaerobic tank 5 as return sludge, and the remainder is transferred to the surplus sludge thickening tank 20 as surplus sludge 14, and separated into surplus sludge thickening tank supernatant liquid 21 and concentrated surplus sludge 22. be done. Further, the first settling tank sludge 3 separated in the first settling tank 2 is concentrated in the first settling sludge concentration tank 15. The degree of concentration of these sludges is preferably such that both sludge concentrations are 1% or more. Next, the concentrated initial settling sludge 17 and the concentrated excess sludge 22 are mixed in a mixing tank 23. When both thickened sludges are mixed, a large amount of phosphorus in the thickened excess sludge 22 is released in a short period of time, so in order to prevent phosphorus release, an iron salt compound 24 is added and mixed, and at the time of mixing.
Add 25% of slaked lime so that the pH becomes 6-8. The amount of iron salt compound 24 added varies depending on the properties of the sludge, but it is necessary to mix 1 to 5% iron based on the solid matter of sludge, and the addition and mixing of iron salt compound 24 and slaked lime 25 is It is preferable to start at the same time as the mixing of the thickened sludge, but if it is within one hour after mixing, the difference in the effect of phosphorus fixation is small, so it is sufficient to start within one hour after mixing. The method for mixing the iron salt compound 24 and the slaked lime 25 is not limited to mixing them in the mixing tank 23, but also a mixer may be provided in the transfer line of the mixing tank thickened sludge 26 to mix them with the thickened sludge. As the iron salt compound 24, it is preferable to use ferrous chloride, ferric chloride, and ferrous sulfate. Moreover, in order to adjust the amount of slaked lime 25 added so that the pH becomes 6 to 8, the slaked lime injection pump 27 may be controlled by the PH meter 28. Next, the mixing tank concentrated sludge 26 mixed with the iron salt compound 24 and slaked lime 25 is introduced into the dehydrator 18, dehydrated, and taken out as a dehydrated cake 29. When dewatering the mixing tank thickened sludge 26, if the sludge is left for a long time, phosphorus will be re-released from the sludge.
It is effective to dehydrate the iron salt compound 24 and slaked lime 25 within 5 hours after addition and mixing, since the phosphorus concentration in the separated liquid 19 can be reduced. As the dehydrator 18 used, a normal dehydrator such as a belt press dehydrator or a centrifugal dehydrator can be used. The dehydrated cake 29 is normally disposed of by drying, incineration, etc. The separated liquid 19 flowing out from the dehydrator 18 is returned and mixed with the liquid to be treated 1 or the supernatant liquid 4 of the initial settling tank 2. The phosphorus concentration in the separated liquid 19 has become low, and the separated liquid 19 is returned to the liquid to be treated 1.
Even if mixed with phosphorus, the inflow phosphorus load will not increase. The second illustrated example is basically the same as the first illustrated example, but a denitrification tank 30 is provided between the anaerobic tank 5 and the aerobic tank 8, and the anaerobic tank outflow mixed liquid 7 of the anaerobic tank 5, A part of the aerobic tank effluent mixed liquid 10 is introduced into the denitrification tank 30 and mixed and stirred to reduce the amount of water contained in the liquid.
While NOx is denitrified, a portion of the soluble phosphorus contained in the anaerobic tank outflow mixed liquid 7 is absorbed into the sludge. Therefore, in the second illustrated example,
Not only can BOD and phosphorus be removed, but nitrogen can also be removed. As described above, in the present invention, the initial settling tank sludge in the first stage of the anaerobic-aerobic activated sludge process and the surplus sludge generated in the anaerobic-aerobic activated sludge process are separately separated and concentrated, and then Simultaneously or immediately after mixing the silted sludge and thickened excess sludge, an iron salt compound is mixed in the range of 1 to 5% iron based on the solids of the mixed sludge, and slaked lime is added so that the pH at the time of mixing is 6 to 8. By mixing and then dehydrating the
This reduces the phosphorus concentration in the separated liquid during dewatering, reduces the amount of phosphorus returned from these sludge treatment systems, and reduces the anaerobic
This prevents an increase in the phosphorus load in the water treatment system of the aerobic activated sludge method, and allows stable phosphorus removal at all times. [Example] Next, an example of the present invention will be shown. Example 1 Domestic sewage discharged from a housing complex was treated as the liquid to be treated by the method shown in the first example. The specifications of each device were as follows. Initial settling tank 2: circular clarifaria water volume 4
m 3 Anaerobic tank 5: Double cylindrical stirring tank Water volume: 4 m 3 Aerobic tank 8: 4-compartment rectangular tank Water volume: 7 m 3 Final settling tank 11: Circular clarifier Water volume:
7m 3 Initial settling sludge thickening tank (gravity type) 15: Circular clarifier Water volume 0.6m 3 Water area 0.15m 2 Excess sludge thickening tank (gravity type) 20: Circular clarifier Water volume 0.6m 3 Water area 0.3m 2 Dehydrator 18 : Centrifugal separator Processing amount: 10Kg/h Using such facilities, the amount of liquid to be processed is 55m 3 /
When the returned sludge 13 was treated at a flow rate of 15.4 m 3 /d, a treated liquid as shown in Table 1 was obtained.

【表】 この時の返送汚泥のMLSS濃度は1.2%、好気
槽のMLSS濃度は2800mg/であつた。 また、余剰汚泥14を410/d余剰汚泥濃縮
槽20に導入し、該濃縮槽からの引き抜き汚泥2
2量を205/dとしたところ、濃縮槽の汚泥界
面は水面下1000mmでほぼ一定であり、濃縮余剰汚
泥22濃度は2.4%であつた。 他方、最初沈殿池汚泥3を初沈汚泥濃縮槽15
に導入し、濃縮汚泥17として濃度3%のものが
312/d得られた。 次に、これらの濃縮余剰汚泥22と濃縮初沈汚
泥17を混合槽23に導入し、塩化第2鉄24を
汚泥固形当り鉄として2.5%注入し、混合槽23
内のPH7.5になるように消石灰25を注入し、15
分間混合したのち直ちに遠心分離機18で脱水を
行つた。消石灰25の添加量は汚泥固形物当り4
%であつた。 その結果は表−2のとおりであつた。 比較例 実施例1における余剰汚泥を最初沈殿池に返送
し、全量を初沈汚泥濃縮槽に導入して濃縮し濃度
2.5%の濃縮初沈汚泥570/dが得られた。次
に、この濃縮汚泥を混合槽に導入し、塩化第2鉄
を汚泥固形物当り鉄として2.5%注入し、混合槽
内のPHが7.5になるように消石灰を注入し、15分
間混合したのち直ちに遠心分離機で脱水を行つ
た。その結果も表−2に示した。
[Table] At this time, the MLSS concentration in the returned sludge was 1.2%, and the MLSS concentration in the aerobic tank was 2800 mg/. In addition, the surplus sludge 14 is introduced into the 410/d surplus sludge thickening tank 20, and the sludge 2 drawn from the thickening tank is
When the amount of sludge 2 was set as 205/d, the sludge interface in the thickening tank was almost constant at 1000 mm below the water surface, and the concentration of thickened surplus sludge 22 was 2.4%. On the other hand, the first settling tank sludge 3 is transferred to the first settling sludge thickening tank 15.
The sludge with a concentration of 3% was introduced as thickened sludge 17.
312/d was obtained. Next, these concentrated excess sludge 22 and concentrated initial settling sludge 17 are introduced into the mixing tank 23, and ferric chloride 24 is injected in an amount of 2.5% as iron per solid sludge.
Inject 25% of slaked lime to make the pH within 15%.
Immediately after mixing for a minute, dehydration was performed using a centrifuge 18. The amount of slaked lime 25 added is 4 per solid sludge.
It was %. The results were as shown in Table-2. Comparative Example The excess sludge in Example 1 was returned to the initial settling tank, and the entire amount was introduced into the initial settling sludge thickening tank to concentrate and reduce the concentration.
A 2.5% concentrated initial settled sludge of 570/d was obtained. Next, this thickened sludge was introduced into a mixing tank, ferric chloride was injected at 2.5% as iron per sludge solids, slaked lime was injected so that the pH in the mixing tank became 7.5, and after mixing for 15 minutes, It was immediately dehydrated using a centrifuge. The results are also shown in Table-2.

【表】【table】

【表】 表−2から、脱水液中のリン濃度は、比較例
が200mg/であつたのに対し、本発明の場合は
2.0mg/であり、また脱水液中の全リン量は
それぞれ89.2g/d、0.9g/dであり、本発明
によれば脱水液中のリン量を顕著に低減させる
ことがわかる。また、被処理液のリン濃度8.3
mg/に対し、比較例では最終処理液中のリン濃
度は4.0mg/cm2であつたのにくらべ、本発明の
最終処理液中のリン濃度は0.7mg/と低く、安
定した処理結果が得られることがわかる。 実施例 2 実施例1における混合槽への塩化第2鉄の注入
量および混合槽内のPHを変化させて種々の条件下
で調整した汚泥を、直ちに遠心分離機で脱水した
処理結果を表−3、4に示す(混合槽における混
合時間はいずれも15分間であり一定とした)。
[Table] From Table 2, the phosphorus concentration in the dehydrated solution was 200mg/in the comparative example, while in the case of the present invention,
The total amount of phosphorus in the dehydrated solution is 89.2 g/d and 0.9 g/d, respectively, indicating that the present invention significantly reduces the amount of phosphorus in the dehydrated solution. In addition, the phosphorus concentration of the liquid to be treated is 8.3
mg/cm2, whereas in the comparative example the phosphorus concentration in the final treatment solution was 4.0mg/ cm2 , the phosphorus concentration in the final treatment solution of the present invention was as low as 0.7mg/cm2, and stable treatment results were obtained. You can see what you can get. Example 2 The sludge prepared under various conditions by changing the amount of ferric chloride injected into the mixing tank and the PH in the mixing tank in Example 1 was immediately dehydrated using a centrifuge. The treatment results are shown in the table below. 3 and 4 (the mixing time in the mixing tank was 15 minutes and constant).

【表】【table】

【表】 この結果、脱水液中のリン濃度は汚泥固形物
あたりの塩化第2鉄の添加量を鉄として1〜5
%、PH6〜8の条件下で混合処理すれば、良好な
結果が得られることがわかる。 実施例 3 実施例2における実験No.3で調整した混合汚泥
(混合時間15分)を、遠心分離機で脱水処理する
までの汚泥の貯留時間と脱水液中のリン濃度の
関係は表−5に示すとおりであつた。
[Table] As a result, the phosphorus concentration in the dehydrated liquid is 1 to 5, with the amount of ferric chloride added per solid sludge being iron.
%, it can be seen that good results can be obtained if the mixing treatment is carried out under conditions of pH 6 to 8. Example 3 Table 5 shows the relationship between the sludge storage time until the mixed sludge (mixing time 15 minutes) prepared in Experiment No. 3 in Example 2 is dehydrated using a centrifuge and the phosphorus concentration in the dehydrated liquid. It was as shown in.

【表】 このように、混合処理後はできるだけ速やかに
(混合処理後5時間以内が好ましい)脱水処理す
るのが有利である。
[Table] Thus, it is advantageous to perform the dehydration treatment as soon as possible after the mixing treatment (preferably within 5 hours after the mixing treatment).

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

第1図は本発明の一実施態様を示す系統説明
図、第2図は本発明の他の実施態様を示す系統説
明図で、第3図は従来方法を示す系統説明図であ
る。 1……被処理液、2……最初沈殿池、3……最
初沈殿池汚泥、4……上澄液、5……嫌気槽、6
……撹拌機、7……嫌気槽流出混合液、8……好
気槽、9……散気器、10……好気槽流出混合
液、11……最終沈殿池、12……処理液、13
……最終沈殿池汚泥、14……余剰汚泥、15…
…初沈汚泥濃縮槽、16……初沈汚泥濃縮槽上澄
液、17……濃縮初沈汚泥、18……脱水機、1
9……分離液、20……余剰汚泥濃縮槽、21…
…余剰汚泥濃縮槽上澄液、22……濃縮余剰汚
泥、23……混合槽、24……鉄塩化合物、25
……消石灰、26……混合槽濃縮汚泥、27……
消石灰注入ポンプ、28……PH計、29……脱水
ケーキ、30……脱窒素槽。
FIG. 1 is a system explanatory diagram showing one embodiment of the present invention, FIG. 2 is a system explanatory diagram showing another embodiment of the present invention, and FIG. 3 is a system explanatory diagram showing a conventional method. 1... Liquid to be treated, 2... First settling tank, 3... First settling tank sludge, 4... Supernatant liquid, 5... Anaerobic tank, 6
...Agitator, 7...Anaerobic tank effluent mixed liquid, 8...Aerobic tank, 9...Aerator, 10...Aerobic tank effluent mixed liquid, 11...Final sedimentation tank, 12...Treatment liquid , 13
...Final settling tank sludge, 14... Surplus sludge, 15...
... Initial settling sludge thickening tank, 16... Initial settling sludge thickening tank supernatant liquid, 17... Concentrated initial settling sludge, 18... Dehydrator, 1
9...separated liquid, 20...excess sludge thickening tank, 21...
... Surplus sludge concentration tank supernatant liquid, 22 ... Thickened surplus sludge, 23 ... Mixing tank, 24 ... Iron salt compound, 25
... Slaked lime, 26 ... Mixing tank thickened sludge, 27 ...
Slaked lime injection pump, 28...PH meter, 29...Dehydration cake, 30...Denitrification tank.

Claims (1)

【特許請求の範囲】 1 被処理液を最初沈殿池で沈殿分離し、該分離
液と返送汚泥とを、溶存酸素、硝酸、亜硝酸のい
ずれもが実質的に存在しない嫌気状態で混合処理
したのち、曝気処理を行い、該曝気混合液を最終
沈殿池で沈殿分離し、該沈殿汚泥の一部を前記返
送汚泥とし、残部を余剰汚泥とする有機性廃液の
生物学的処理方法において、最初沈殿池汚泥と最
終沈殿池からの前記余剰汚泥をそれぞれ別個に濃
縮し、これら両方の濃縮汚泥を混合すると同時に
又は混合直後に鉄塩化合物を鉄として汚泥固形物
当り1〜5%添加し、かつそのPHが6〜8になる
ように消石灰を添加混合処理したのち、脱水処理
を行うことを特徴とする有機性廃液の処理方法。 2 前記最初沈殿池汚泥及び最終沈殿池からの余
剰汚泥をそれぞれ別個に濃縮するに際し、それぞ
れの汚泥濃度を1%以上とするものである特許請
求の範囲第1項記載の有機性廃液の処理方法。 3 前記濃縮汚泥の混合処理後、5時間以内に脱
水処理を行うものである特許請求の範囲第1項又
は第2項記載の有機性廃液の処理方法。
[Scope of Claims] 1. The liquid to be treated is first separated by sedimentation in a settling tank, and the separated liquid and returned sludge are mixed in an anaerobic state in which dissolved oxygen, nitric acid, and nitrous acid are substantially absent. Afterwards, an aeration treatment is performed, and the aerated mixture is separated by sedimentation in a final settling tank, a part of the settled sludge is used as the return sludge, and the remainder is used as surplus sludge. The sedimentation tank sludge and the surplus sludge from the final sedimentation tank are each concentrated separately, and at the same time or immediately after mixing both of these thickened sludges, an iron salt compound is added as iron in an amount of 1 to 5% based on the sludge solids, and A method for treating an organic waste liquid, which comprises adding and mixing slaked lime so that the pH thereof becomes 6 to 8, and then dehydrating the liquid. 2. The method for treating organic waste liquid according to claim 1, wherein when the excess sludge from the first settling tank sludge and the final settling tank are concentrated separately, the sludge concentration of each is set to 1% or more. . 3. The method for treating organic waste liquid according to claim 1 or 2, wherein dehydration treatment is performed within 5 hours after the mixing treatment of the thickened sludge.
JP59246122A 1984-11-22 1984-11-22 Treatment of organic waste liquid Granted JPS61125489A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59246122A JPS61125489A (en) 1984-11-22 1984-11-22 Treatment of organic waste liquid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59246122A JPS61125489A (en) 1984-11-22 1984-11-22 Treatment of organic waste liquid

Publications (2)

Publication Number Publication Date
JPS61125489A JPS61125489A (en) 1986-06-13
JPS6345639B2 true JPS6345639B2 (en) 1988-09-09

Family

ID=17143808

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59246122A Granted JPS61125489A (en) 1984-11-22 1984-11-22 Treatment of organic waste liquid

Country Status (1)

Country Link
JP (1) JPS61125489A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5828208B2 (en) * 2011-02-10 2015-12-02 栗田工業株式会社 Sludge dewatering method

Also Published As

Publication number Publication date
JPS61125489A (en) 1986-06-13

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