JPH0352697A - Treatment of organic sewage containing ammonia - Google Patents

Treatment of organic sewage containing ammonia

Info

Publication number
JPH0352697A
JPH0352697A JP1184465A JP18446589A JPH0352697A JP H0352697 A JPH0352697 A JP H0352697A JP 1184465 A JP1184465 A JP 1184465A JP 18446589 A JP18446589 A JP 18446589A JP H0352697 A JPH0352697 A JP H0352697A
Authority
JP
Japan
Prior art keywords
sludge
solid
liquid
separated
supplied
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.)
Granted
Application number
JP1184465A
Other languages
Japanese (ja)
Other versions
JPH0549359B2 (en
Inventor
Katsuyuki Kataoka
克之 片岡
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 JP1184465A priority Critical patent/JPH0352697A/en
Publication of JPH0352697A publication Critical patent/JPH0352697A/en
Publication of JPH0549359B2 publication Critical patent/JPH0549359B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/10Biological treatment of water, waste water, or sewage

Landscapes

  • Activated Sludge Processes (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

PURPOSE:To clean sewage in a short period of time at a high degree and to obtain the economical treatment method by biologically treating the sewage and subjecting sludge to a solid-liquid separation, then adding an alkali to the sludge and biologically treating the sewage together with the sludge and executing ammonia stripping. CONSTITUTION:Descummed night soil 1 is supplied into an activated sludge aeration tank 2 where BOD is removed by the activated sludge of a high concn. while an oxygen-contg. gas is supplied. Activated sludge slurry 4 is then supplied to a solid-liquid sepn. stage 5 and is separated to separated sludge 6 and supernatant separated water 7. A part 8 of the solid-liquid separated sludge 6 or the sludge 8''' withdrawn from the activated sludge aeration tank 2 is introduced into an intimate mixing and stagnating tank 9 where the alkaline agent 10, such as NaOH, is added to the sludge to solubilize the cell constituting materials, such as polysaccharides, contained in the sludge. This sludge is supplied into a biological treating tank 2. The solid-liquid separated water 7 is brought into counter current contact with air or steam 13 to strip the NH3-N in the solid-liquid separated water 7.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、有機性汚水の処理方法に係り、特に、し尿な
どのNH.一Nを含む有機性汚水の新規な処理方法に関
する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for treating organic sewage, and in particular to a method for treating NH. The present invention relates to a novel method for treating organic wastewater containing -N.

〔従来の技術〕[Conventional technology]

従来、NH3−N含有有機性排水の処理法として、最も
代表的な方法は、生物学的硝化脱窒素法であるが、この
方法は、硝化脱窒反応速度が小さいため、大容量の処理
槽(し尿処理の場合は滞留日数9〜lO日の生物処理槽
を要する)を必要とし、また余剰生物汚泥の発生量が多
く、汚泥処理に、大がかりな設備と高額の運転コストを
必要とするという2大欠点がある。
Conventionally, the most typical method for treating organic wastewater containing NH3-N is biological nitrification and denitrification, but this method requires a large-capacity treatment tank because the nitrification and denitrification reaction rate is slow. (In the case of human waste treatment, a biological treatment tank with a residence time of 9 to 10 days is required), and a large amount of surplus biological sludge is generated, requiring large-scale equipment and high operating costs for sludge treatment. There are two major drawbacks.

また、NH3−Hの物理化学的な舛理法として、アルカ
リ条件下でのNH.ストリップ法が公知であるが、この
方法は、NaOH. Ca (DH) 2などのアルカ
リを多量に必要とし、運転コストが著しく高いという欠
点があった。
In addition, as a physicochemical method for NH3-H, NH3-H under alkaline conditions. The strip method is known, but this method uses NaOH. It has the drawback that it requires a large amount of alkali such as Ca (DH) 2 and the operating cost is extremely high.

また、了ンモニ了ストリップ法は、BODを除去できず
、また種々の窒素或分のうちNH.−Nしか除去できな
いため、生物学的硝化脱窒工程を後続して付加する必要
があるが、この生物処理工程からの余剰汚泥の発生量が
多いという欠点がある。
In addition, the strip method cannot remove BOD and contains a certain amount of NH. Since only -N can be removed, it is necessary to subsequently add a biological nitrification-denitrification process, but this biological treatment process has the disadvantage of generating a large amount of surplus sludge.

〔発明が解決しようとする課題] 本発明は、上記したような従来技術の問題点を大幅に改
善し、し尿などのNH.−Nを含む有機性排水を、短時
間で高度に浄化するとともに、排水処理に伴って発生す
る余剰生物汚泥の量を著しく減少させることができる経
済的な新しい処理方法を提供することを目的とする。
[Problems to be Solved by the Invention] The present invention significantly improves the problems of the prior art as described above, and eliminates NH. - The objective is to provide a new economical treatment method that can highly purify organic wastewater containing N in a short time and significantly reduce the amount of surplus biological sludge generated during wastewater treatment. do.

〔課題を解決するための手没〕[Working hard to solve the problem]

上記目的を達或するために、本発明では、(a),アン
モニアを含む有機性汚水を生物処理する工程、(b).
工程(a)からの生物処理スラツジを固液分離する工程
、(c),工程(b)で固液分離された汚泥の少なくと
も一部、あるいは工程(a)から引抜いた汚泥にアルカ
リを添加し、常温又は加温条件下で混和滞留する工程、
(d).工程(c)からの処理汚泥を、工程(a)で有
機性汚水と共に生物処理する工程、(e).工程b)で
固液分離された分離水に空気又はスチームを供給してア
ンモニアストリッピングする工程、の各工程を順次行な
うことによるアンモニアを含む有機性汚水の処理方法と
したものである。
In order to achieve the above object, the present invention includes (a) a step of biologically treating organic wastewater containing ammonia; (b).
A step of separating the biologically treated sludge from step (a) into solid-liquid, (c) adding an alkali to at least a part of the sludge separated into solid-liquid in step (b) or the sludge drawn from step (a). , a step of mixing and retaining at room temperature or under heated conditions;
(d). Biologically treating the treated sludge from step (c) together with organic wastewater in step (a); (e). This is a method for treating organic wastewater containing ammonia by sequentially carrying out each step of ammonia stripping by supplying air or steam to the solid-liquid separated separated water in step b).

次に、本発明を、図面を参照にしながら詳述する。Next, the present invention will be explained in detail with reference to the drawings.

第1図は、本発明の処理方法の一例を示すフローエ程図
である。ここでは、し尿処理を例に挙げて説明する。
FIG. 1 is a flow diagram showing an example of the processing method of the present invention. Here, human waste treatment will be explained as an example.

第l図において、除渣し尿1を活性汚泥曝気槽2に供給
し、酸素供給装置3から酸素含有ガスを供給しつつ高濃
度の活性汚泥によって、B○Dを除去したのち、活性汚
泥スラリ−4を固液分離工程5 (図示例はUF膜分離
装置)に供給して、分離汚泥6と清澄分離水7に分離す
る。
In Fig. 1, removed human waste 1 is supplied to an activated sludge aeration tank 2, and B○D is removed by high-concentration activated sludge while supplying oxygen-containing gas from an oxygen supply device 3. 4 is supplied to a solid-liquid separation step 5 (the illustrated example is a UF membrane separator) and separated into separated sludge 6 and clear separated water 7.

し尿無希釈処理の場合、曝気槽温度は生物酸化熱によっ
て42〜48℃に上昇した。
In the case of the undiluted human waste treatment, the aeration tank temperature rose to 42-48°C due to the heat of biooxidation.

次に、固液分離汚泥6の一部8又は活性汚泥曝気槽2か
ら引抜いた汚泥8〜を、混和滞留槽9に導き、NaOH
などのアルカリ剤10を添加し、好ましくはp1{10
以上、温度50〜10(1℃に加温しつつ、1〜3時間
程度混和しつつ滞留せしめ、汚泥中に含まれるポリサッ
カライドなどの細胞構或物質を可溶化する。
Next, a part 8 of the solid-liquid separated sludge 6 or the sludge 8 drawn out from the activated sludge aeration tank 2 is introduced into a mixing and retention tank 9, and the NaOH
10 of an alkaline agent such as p1{10
As described above, while heating the sludge to a temperature of 50 to 10°C (1°C), the sludge is mixed and retained for about 1 to 3 hours to solubilize cellular substances such as polysaccharides contained in the sludge.

次に、該アルカリ処理を受けた汚泥(アルカリ性を示す
)11を生物処理槽2に供給する。
Next, the sludge (alkaline) 11 that has undergone the alkali treatment is supplied to the biological treatment tank 2.

つまり、生物処理槽2には、原水1とアルカリ処理汚泥
1lの両者が流入し、これらのBOD成分が除去される
That is, both the raw water 1 and 1 liter of alkali-treated sludge flow into the biological treatment tank 2, and their BOD components are removed.

生物処理槽2のpHは、アルカリ処理汚泥11の流入に
より、アルカリ性を示し、また固液分離処理水7もアル
カリ性を示す。
The pH of the biological treatment tank 2 is alkaline due to the inflow of the alkali-treated sludge 11, and the solid-liquid separation treated water 7 is also alkaline.

なお、8′は、アルカリ処理を受けないで、生物処理槽
2に返送される汚泥であり、8′は汚泥脱水工程に導か
れて処分される余剰汚泥である。本発明では、余剰汚泥
8′の発生量は、非常に少なくなるという特記すべき効
果がある。
Note that 8' is sludge that is returned to the biological treatment tank 2 without being subjected to alkali treatment, and 8' is excess sludge that is led to a sludge dewatering step and disposed of. The present invention has the noteworthy effect that the amount of surplus sludge 8' generated is extremely reduced.

しかして、以上のような方法に従って運転操作された固
液分離水7を、必要によりアルカリ剤を添加して充填塔
などの気液接触塔l2の上部に導き、下向流で、流下さ
せ空気またはスチーム13と向流接触せしめ、固液分離
水7中のN H . − Nをストリッピングする。
The solid-liquid separated water 7 operated according to the method described above is introduced into the upper part of the gas-liquid contact tower 12 such as a packed tower, with an alkaline agent added thereto if necessary, and allowed to flow downward to absorb air. Alternatively, the N H . - Stripping N.

前述の如く、アルカリ処理汚泥の流入に起因して、固液
分離水7のpHはアルカリ性を示し、かつ、生物酸化熱
によって水温40℃になるのでN}13−Nは効率的に
ス}IJップ除去される。通常の場合は汚泥のアルカリ
処理槽9に注入されるNaOHだけで、固液分離水7の
pifはN H 3− Nのストリッピングに好適なp
H9.0以上になるが、原水の水質によって、固液分離
水のpHが9未満になる場合は、少量のNaOHを気液
接触塔の流入水7に補給しても良いことは申すまでもな
い。
As mentioned above, due to the inflow of alkali-treated sludge, the pH of the solid-liquid separated water 7 becomes alkaline, and the water temperature reaches 40°C due to the heat of biological oxidation, so that N}13-N is efficiently converted to S}IJ. is removed. In normal cases, only NaOH is injected into the sludge alkaline treatment tank 9, and the pif of the solid-liquid separated water 7 is a pif suitable for stripping NH3-N.
However, if the pH of the solid-liquid separated water becomes less than 9 depending on the quality of the raw water, it goes without saying that a small amount of NaOH may be added to the inflow water 7 of the gas-liquid contact tower. do not have.

しかして、BOD,SS,NH3−Nが高度に除去され
た処理水14が、アンモニアス} IJツプ塔の下部か
ら流出し、必要に応じ凝集分離、活性炭、03処理など
のCOD除去処理16を施したのち、公共用水域に放流
される。
The treated water 14 from which BOD, SS, and NH3-N have been highly removed flows out from the lower part of the ammonia IJ column and is subjected to COD removal treatment 16 such as coagulation separation, activated carbon treatment, and 03 treatment as necessary. After treatment, the water is released into public waters.

なお、ストリップ塔から放散されるN113含有ガス1
5は、触媒燃焼、酸による吸収など公知手段17によっ
て処理され、無害化される。
In addition, N113-containing gas 1 released from the stripping tower
5 is treated by known means 17 such as catalytic combustion or absorption with acid to render it harmless.

〔実施例〕〔Example〕

以下、実施例により本発明をよ゛り具体的に説明するが
、本発明はこれに限定されるものではない。
EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited thereto.

実施例1 し尿を対象として、本発明を第1図のフローに従って実
施した。
Example 1 The present invention was carried out using human waste according to the flow shown in FIG.

表−1に示す水質の除渣し尿1と後記のアルカリ処理汚
泥11の両者を、表−2の運転条件によって活性汚泥処
理をした。
Both the desalted night soil 1 having the water quality shown in Table 1 and the alkali-treated sludge 11 described later were subjected to activated sludge treatment under the operating conditions shown in Table 2.

表 2 活性汚泥処理の曝気槽運転 条件 曝気槽2より流出する活性汚泥4を、チューブラ型の限
外ろ過膜5により、膜分離し、表3の膜透過水7を得た
Table 2 Aeration tank operating conditions for activated sludge treatment Activated sludge 4 flowing out from the aeration tank 2 was subjected to membrane separation using a tubular type ultrafiltration membrane 5 to obtain membrane permeated water 7 shown in Table 3.

UF膜の分両分子量は10万、UP膜材質はポリオレフ
ィンのものを使用した。またUP膜で分離された汚泥6
の固形物濃度は2.2〜2.3%であった。
The molecular weight of the UF membrane was 100,000, and the material of the UP membrane was polyolefin. In addition, sludge separated by UP membrane6
The solids concentration was 2.2-2.3%.

表−3 UF膜透過水の水質 次に、UP分離汚泥6の50%を分取8し、これを混和
滞留槽9に導き、NaOH10を加えp+12の条件で
、温度70℃に加温し、4hr攪拌しながら滞留せしめ
たのち、酸で中和することなく、活性汚泥処理工程の曝
気槽2に供給した。
Table 3 Water quality of UF membrane permeated water Next, 50% of the UP separated sludge 6 was fractionated 8 and introduced into the mixing and retention tank 9, where NaOH 10 was added and heated to a temperature of 70°C under the condition of p+12. After being allowed to stay with stirring for 4 hours, it was supplied to the aeration tank 2 of the activated sludge treatment process without being neutralized with acid.

NaOflの所要注入率は、し尿11j2あたり、6〜
8 kgであった。
The required injection rate of NaOfl is 6 to 6 per human waste 11j2.
It weighed 8 kg.

tJF膜分離汚泥の残り8′の50%は、アルカリ処理
をほどこさずに、曝気槽2に返送した,このような操作
条件を5ケ月継続して行ったときの、余剰汚泥8′発生
量の平均値は1.2kg ss/ k l L.尿であ
ッタ。
50% of the remaining 8' of JF membrane-separated sludge was returned to aeration tank 2 without alkali treatment.The amount of surplus sludge 8' generated when these operating conditions were continued for 5 months. The average value is 1.2 kg ss/k l L. It's full of urine.

この値は、従来法の余剰汚泥発生M5〜7kg ss/
 k IlL,尿に比較して、大幅に少ないものであっ
た。
This value is based on the excess sludge produced by the conventional method M5~7kg ss/
kIIL, was significantly lower than that in urine.

次に、表−3の水質をもつUP透過水7をテラレット(
日鉄化工(株)商品)を充填した高さ10mの充填塔l
2の上部に供給し、充填塔内を下向流で流下させつつ、
下部より、温度50℃の空気13を気液比(G/L)=
2.5で供給した。
Next, the UP permeated water 7 having the water quality shown in Table 3 was mixed with Terraret (
A 10m high packed tower filled with Nippon Steel Kako Co., Ltd. product)
2, while flowing downward in the packed column,
From the bottom, air 13 at a temperature of 50°C is added to the gas-liquid ratio (G/L) =
2.5.

なお、Lは原水流量(m’/Hr) Gは空気の質量流量(kg/Hr)を意味す。In addition, L is the raw water flow rate (m’/Hr) G means air mass flow rate (kg/Hr).

この結果、気液接触塔流出水14の水質は、表−4の如
くになった。
As a result, the quality of the gas-liquid contact tower effluent water 14 was as shown in Table 4.

表−4 気液接触塔流出水の水質 〔発明の効果〕 本発明によれば、次のような特筆すべき効果が得られる
Table 4 Water quality of gas-liquid contact tower effluent [Effects of the invention] According to the present invention, the following noteworthy effects can be obtained.

■ 余剰汚泥発生量が大きく減少する。■ The amount of surplus sludge generated is greatly reduced.

その結果、汚泥処理、汚泥処分が著しく合理化される。As a result, sludge treatment and sludge disposal are significantly streamlined.

汚泥脱水助剤(ボリマなど)も大きく節減される。Sludge dewatering aids (such as Borima) are also significantly saved.

■ 汚泥の可溶化処理に使用したアルカリ剤を利用して
、NH3ス} IJップ工程への流入水のpHを自動的
に高くできる。その結果、実質的にNH3ストリップの
ためのアルカリ剤が不要になり、運転コストが大きく減
少する。
■Using the alkaline agent used in the sludge solubilization process, the pH of the water flowing into the NH3/IJ process can be automatically raised. As a result, there is virtually no need for an alkaline agent for the NH3 strip, greatly reducing operating costs.

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

第1図は、本発明の一例を示すフロー工程図である。 1・・・原水、2・・・生物処理槽、3・・・酸素供給
装置、4・・・活性汚泥スラリ− 5・・・固液分離工
程、6・・・分離汚泥、7・・・清澄分離水、8、8′
8′ 8″・・・分離汚泥、9・・・混和滞留槽、10
・・・アルカリ剤、l1・・・アルカリ処理汚泥、l2
・・・気液接触塔、13・・・空気又はスチーム、14
・・・処理水、15・・・アンモニア含有ガス、16・
・・COD除去処理、17・・・アンモニア分離処理
FIG. 1 is a flow process diagram showing an example of the present invention. 1... Raw water, 2... Biological treatment tank, 3... Oxygen supply device, 4... Activated sludge slurry 5... Solid-liquid separation process, 6... Separated sludge, 7... Clear separated water, 8, 8'
8'8''... Separated sludge, 9... Mixing and retention tank, 10
... Alkali agent, l1... Alkali treated sludge, l2
... Gas-liquid contact tower, 13 ... Air or steam, 14
... Treated water, 15 ... Ammonia-containing gas, 16.
・・COD removal process, 17... Ammonia separation process

Claims (1)

【特許請求の範囲】 1、(a)、アンモニアを含む有機性汚水を生物処理す
る工程、 (b)、工程(a)からの生物処理スラッジを固液分離
する工程、 (c)、工程(b)で固液分離された汚泥の少なくとも
一部、あるいは、工程(a)から引抜いた汚泥にアルカ
リを添加し、常温又は加温条件 下で混和滞留する工程、 (d)、工程(c)からの処理汚泥を、工程(a)で有
機性汚水と共に生物処理する工程、 (e)、工程(b)で固液分離された分離水に空気又は
スチームを供給してアンモニアストリッピングする工程
、 の各工程を順次行なうことを特徴とするアンモニアを含
む有機性汚水の処理方法。
[Claims] 1. (a) A step of biologically treating organic sewage containing ammonia, (b) A step of solid-liquid separation of the biologically treated sludge from step (a), (c) A step ( Step (d), step (c) of adding an alkali to at least a portion of the sludge separated into solid-liquid in b) or the sludge drawn out from step (a), and mixing and retaining it at room temperature or under heated conditions; (a) biologically treating the treated sludge together with organic wastewater in step (a); (e) supplying air or steam to the solid-liquid separated water in step (b) for ammonia stripping; A method for treating organic wastewater containing ammonia, characterized by sequentially performing each step.
JP1184465A 1989-07-19 1989-07-19 Treatment of organic sewage containing ammonia Granted JPH0352697A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1184465A JPH0352697A (en) 1989-07-19 1989-07-19 Treatment of organic sewage containing ammonia

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1184465A JPH0352697A (en) 1989-07-19 1989-07-19 Treatment of organic sewage containing ammonia

Publications (2)

Publication Number Publication Date
JPH0352697A true JPH0352697A (en) 1991-03-06
JPH0549359B2 JPH0549359B2 (en) 1993-07-26

Family

ID=16153630

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1184465A Granted JPH0352697A (en) 1989-07-19 1989-07-19 Treatment of organic sewage containing ammonia

Country Status (1)

Country Link
JP (1) JPH0352697A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4911813A (en) * 1972-04-12 1974-02-01
JPS5020565A (en) * 1973-06-27 1975-03-04

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4911813A (en) * 1972-04-12 1974-02-01
JPS5020565A (en) * 1973-06-27 1975-03-04

Also Published As

Publication number Publication date
JPH0549359B2 (en) 1993-07-26

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