JPS5929092A - Treatment of sewage containing nitrogen component - Google Patents
Treatment of sewage containing nitrogen componentInfo
- Publication number
- JPS5929092A JPS5929092A JP14043282A JP14043282A JPS5929092A JP S5929092 A JPS5929092 A JP S5929092A JP 14043282 A JP14043282 A JP 14043282A JP 14043282 A JP14043282 A JP 14043282A JP S5929092 A JPS5929092 A JP S5929092A
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- Prior art keywords
- tank
- denitrification
- sewage
- treatment
- acid
- 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.)
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Abstract
Description
【発明の詳細な説明】
この発明は、窒素成分を含む汚水、例えばし尿、下水、
その他の産業廃水、あるいはし尿処理場などから発生す
る汚泥、その他の有機性廃1″′(′″Tj;hl;’
!i:JIK IM*J 8’p ) k% 。DETAILED DESCRIPTION OF THE INVENTION The present invention provides waste water containing nitrogen components, such as human waste, sewage,
Other industrial wastewater, sludge generated from human waste treatment plants, and other organic waste 1''('''Tj;hl;'
! i: JIK IM*J 8'p) k%.
物学的に脱窒処理する方法に関する。This invention relates to a method for physically denitrifying treatment.
近年、排水処理基準の高度化に伴い、脱窒処理まで要求
されるようになっている。例えば、 1し尿処
理においては、低希釈あるいは無希釈の汚水を生物学的
に硝化脱窒処理する方式も採用されている。In recent years, as wastewater treatment standards have become more sophisticated, denitrification treatment has become required. For example, in human waste treatment, a method is also adopted in which low-diluted or undiluted wastewater is biologically treated by nitrification and denitrification.
従来の生物学的脱窒法としては、汚水を嫌気性の脱窒槽
、好気性の硝化槽に順次通水するとともに、硝化槽から
の硝化液のかなりの量を脱窒槽に返送循環し、脱窒槽で
の水素供与体として汚水中の有機物を用いることにより
BOD除去と脱窒処理を行う方法、あるいは、汚水を硝
化槽でアンモニア性窒素を酸化し、次にメタノールなど
の有機物を添加しなから脱窒槽においで還元する形式な
どが採用されている。In the conventional biological denitrification method, wastewater is sequentially passed through an anaerobic denitrification tank and an aerobic nitrification tank, and a considerable amount of the nitrified liquid from the nitrification tank is circulated back to the denitrification tank. A method of removing BOD and denitrification by using organic matter in wastewater as a hydrogen donor, or oxidizing ammonia nitrogen from wastewater in a nitrification tank, and then denitrifying it without adding organic matter such as methanol. Methods such as reduction in a nitrogen tank are adopted.
一方、最近のエネルギー事情から、汚水を好気性処理方
式から、プロツーなどの使用ヲ能なb ナイ7ンニンク
゛コストの安い処理法である嫌気性処理法が注目されて
いる。この嫌気性処理は、汚泥の発生量が少なく、捷た
、メタンガスとしてエネルギー回収できる利af持って
いる。On the other hand, due to the recent energy situation, attention has been paid to an anaerobic treatment method, which is a low-cost treatment method, instead of an aerobic treatment method for wastewater. This anaerobic treatment has the advantage of generating less sludge and recovering energy as methane gas.
さらに、この嫌気性処理も、先ず有機1住汚水中の有機
物を嫌気tL液化青IU’fl腐敗閑群ンの作用により
、酢酸、フロピオン酸、酪酸などの押発註有機酸にする
酸生成反応、と、これら生成した櫓(殉酸かメタン4ト
成菌Qてよって、メタンに転換するガース化反応(メタ
ン生成反応)の、二相に分けた二相嫌気性処理法が1是
案されている。Furthermore, in this anaerobic treatment, the organic matter in the sewage is first converted into extruded organic acids such as acetic acid, phlopionic acid, and butyric acid through the action of anaerobic tL liquefaction blue IU'fl putrefaction. A two-phase anaerobic treatment method has been proposed in which the gas formation reaction (methane production reaction), which converts the produced turrets (acid acid or methane) into methane, into two phases. ing.
この二相嫌気性処理法は、従来の一槽内で嫌気(消化〕
処理をf工う1光導消化法に比べ、処理と、それに梳く
メタン生成反応をさらに研究したところ、硫酸塩還元細
菌を利用することにより、処理効率をより促進させる知
見を得るとともに、嫌気処理工程て発生する1飽化水素
を用いて自栄養細閉により、脱窒反応を行なわせること
により、汚水を嫌気性処理しつつ、脱窒(素)処理をも
可能とした、汚水の有効な処理方法を提案するに至った
。This two-phase anaerobic treatment method uses conventional anaerobic (digestion) in one tank.
In comparison to the one-light induction digestion method, which requires multiple processing steps, further research into the treatment and the methane production reaction involved in combing it revealed that by using sulfate-reducing bacteria, the treatment efficiency could be further promoted, and the anaerobic treatment process could be improved. An effective treatment for wastewater that enables denitrification (elementary) treatment while treating wastewater anaerobically by performing a denitrification reaction through autotrophic microsealization using monosaturated hydrogen generated by We have proposed a method.
上述の嫌気性処理法においては、酸生成反応とメタン生
成反応を有している。このうち、酸生成反応において生
成される酢酸以外の酸、例えばフロピオン酸などは、メ
タン生成菌によってメタンへ転換される速度が遅く、い
わゆる反応律速となっている。The above-mentioned anaerobic treatment method includes an acid production reaction and a methane production reaction. Among these, acids other than acetic acid produced in the acid production reaction, such as fropionic acid, are converted to methane by methanogens at a slow rate, which is the so-called rate-limiting reaction.
したがって、酸生成反応の段階でプロピオン酸などを酢
酸の形まで分解しておくことが、嫌気性処理効率を高め
ることとなる。Therefore, decomposing propionic acid and the like into acetic acid at the stage of the acid production reaction increases the efficiency of anaerobic treatment.
グロピレン酸、酪酸あるいは乳酸などを酢酸まで分解す
るためには、デスルホビブリオ(1)es Lll f
o−vibrio)あるいはテスルホマクラム(Des
ulfo−maculum )などの硫酸塩還元細菌が
有効であり、ここでこの細菌に利用されるイオウ化合物
としては、嫌気処理工程から得られる硫化水素全酸化し
て得ることができるとともに、SOニー+52o2+−
などの他のイオウ酸化物を用いることも可能である。In order to decompose glopyrenic acid, butyric acid, lactic acid, etc. to acetic acid, desulfovibrio (1) es Lll f
o-vibrio) or tesulfomacrum (Des
Sulfate-reducing bacteria such as ulfo-maculum) are effective, and the sulfur compounds used by these bacteria can be obtained by total oxidation of hydrogen sulfide obtained from an anaerobic treatment process, and SO ni+52o2+-
It is also possible to use other sulfur oxides such as.
上述のフロピオン酸を硫酸塩還元細菌によるf流酸1盆
還元反応は、次代に示される。The above-mentioned reduction reaction of flopionic acid by sulfate-reducing bacteria will be shown in the next step.
−C)(、C112CO(J−1−112(J+−71
12CO,I SOイー3.3
4 − 11 5
3+Cl3COO−1−Co、、l
ll2S−)−H20+7HCO,、−1フ0H−3
32
以上の式かd明らかなようにフロピオン酸は、酢酸1で
分解され、このときフロピオン酸1モルに対し、硫酸イ
オン1モルを・必要とする。-C)(,C112CO(J-1-112(J+-71
12CO, ISO 3.3 4 - 11 5
3+Cl3COO-1-Co,,l
ll2S-)-H20+7HCO,,-1F0H-3
32 As is clear from the above formula, fropionic acid is decomposed with 1 mole of acetic acid, and at this time, 1 mole of sulfate ion is required per 1 mole of fluopionic acid.
有機注廃准全嫌気注処理するときの、この硫酸イオンの
添υ11搦は、廃液中の有機1住炭素((χ・Jし、0
:3〜3倍(モル比)以上の州ヲ存在させることにより
、各種有機酸を効果的に酢酸まで分解することができる
。When carrying out semi-total anaerobic injection treatment, the addition of sulfate ions is equivalent to the amount of organic carbon ((χ・J, 0) in the waste liquid.
: By having 3 to 3 times (molar ratio) or more of the acid present, various organic acids can be effectively decomposed into acetic acid.
このような硫酸還元反応は、嫌気性処理工程とができる
1、つまり、酸生成反応槽に、硫酸イオンなどのイオウ
化合物を上述した量添加し、従来の酸生成反応と同様に
嫌気的に混合攪拌することにより、有機物を酢酸の形に
まで分解さすことができる。この反応操作は、従来の酸
生成反応と同じでよく、また、これに続くメタン生成反
応も従来どおりでよい。Such a sulfuric acid reduction reaction can be carried out as an anaerobic treatment step 1. In other words, sulfur compounds such as sulfur ions are added in the above-mentioned amount to an acid-producing reaction tank, and mixed anaerobically in the same manner as in conventional acid-producing reactions. By stirring, organic matter can be decomposed into acetic acid form. This reaction operation may be the same as the conventional acid production reaction, and the subsequent methane production reaction may also be the same as the conventional one.
したがって、メ“タン生成槽においては、主として酢酸
をメタンに転換すればよいので、効果的にメタンガスケ
得ることができる。このため、従来法に比べ2〜3割反
応を速めることができるので、処理反応槽容量も小さく
することが6J能となる。Therefore, in the methane production tank, methane gas can be effectively obtained by mainly converting acetic acid into methane.As a result, the reaction can be sped up by 20 to 30% compared to conventional methods. The capacity of 6J can be achieved by reducing the capacity of the processing reaction tank.
さて、自栄養細菌、例えばチオバ/ルステニトリフイカ
ンヌ(Th1obacil’lus denitrif
1cans)などの脱窒細菌は、硫化水素(H2S)
、硫化ノータ頁Nン支、S)、イオウ(SO)あるいは
、SOミー、520H−などの被酸化性イオウ化合物を
利用して水素供与体とし、硝酸性窒素を窒素ガスに1で
還元して脱窒ヲ行う。この反応を下式に示せば次のよう
になる。Now, autotrophic bacteria, such as Th1obacil'lus denitrif
Denitrifying bacteria such as 1cans) produce hydrogen sulfide (H2S).
, sulfide, sulfur (SO), or an oxidizable sulfur compound such as SOMI, 520H- is used as a hydrogen donor, and nitrate nitrogen is reduced to nitrogen gas by 1. Perform denitrification. This reaction can be expressed as follows.
0.42 zH2S−1−(1,422H8−+N01
−+〇、347 Co2−t−o、o s 6 sNH
,++o、56sHco;−+0.8443o2−+0
.5N2+0.865C,H7Co240.4 PI
9)(”
この式から明らかなように、硝酸(NO;) ]モルに
対し、硫酸イオン(807月]844モルが必要である
。0.42 zH2S-1-(1,422H8-+N01
-+〇, 347 Co2-t-o, o s 6 sNH
,++o,56sHco;-+0.8443o2-+0
.. 5N2+0.865C, H7Co240.4 PI
9) ("As is clear from this formula, 844 moles of sulfate ion (807 months) are required for every mol of nitric acid (NO;).
この硫酸イオンは、前記した汚水の嫌気性処理工程で発
生する硫化水素を用いることができる。場合によっては
、硫化水素全アルカリ溶液に通して鈍化ソーダの形にし
て添υII してもよい。As this sulfate ion, hydrogen sulfide generated in the above-described anaerobic treatment process of wastewater can be used. In some cases, hydrogen sulfide may be added in the form of a desensitized soda by passing it through an all-alkaline solution.
もちろん−1不則分は他のイオウあるいはイオウ化合物
を添υ11シて、脱窒反応が円(けに行なわれるように
配j復することが必要である。Of course, it is necessary to add other sulfur or sulfur compounds to the -1 irregularity and to arrange the denitrification reaction in a circular manner.
前者の硫酸塩還元細菌による嫌気性処理工程と、後者の
イオウ卸(閑による脱窒工程を連続して行なわせること
により、効果的な汚水処理を行うことができる。Effective sewage treatment can be achieved by consecutively performing the former anaerobic treatment step using sulfate-reducing bacteria and the latter denitrification step using sulfur removal (vacuum).
すなわち、本発明は、窒素成分を含む汚水ケ嫌気性処理
上梶で処理し、次いで硝化脱窒工程で処理するエイ?か
らなり、嫌気性処理工程で発生する硫化水素を硝化脱窒
工程の脱窒反応槽へ供給することを特徴とするものであ
る。That is, the present invention provides a method for treating wastewater containing nitrogen components in an anaerobic treatment system, and then in a nitrification-denitrification process. It is characterized by supplying hydrogen sulfide generated in the anaerobic treatment process to the denitrification reaction tank of the nitrification and denitrification process.
本発明を実施するのに好適な処理フローラ、第1図及び
第2図に示す。A process flora suitable for carrying out the invention is shown in FIGS. 1 and 2.
第1図に示す処理フローにおいて、汚水は先ず酸生成槽
に受は入れられて汚水中の有機物は、有機酸生成細菌の
他に硫酸塩還元細菌の存在の下に、嫌気的に所定〆晶度
、所定pHに維持されながら混合攪拌されて、酢酸の形
1でに効果的に分解される。ここにおけるfAMイオン
の添加は、この酸生成槽から発生する硫化水素ケ酸化し
て用いるようになっている。もちろん不足分は他のイオ
ウ化合物を流用しても差支ない。In the treatment flow shown in Figure 1, wastewater is first received in an acid generation tank, and organic matter in the wastewater is anaerobically crystallized in the presence of sulfate-reducing bacteria in addition to organic acid-producing bacteria. The mixture is then mixed and stirred while maintaining a predetermined pH, and is effectively decomposed into acetic acid form 1. The fAM ions added here are used by oxidizing hydrogen sulfide generated from this acid generation tank. Of course, you can use other sulfur compounds to make up for the shortage.
醐生成槽において、主として酢酸まで分解された酸生成
#、は、メタン生成槽に送られ、ここで所定温度、所y
jZpHに維持されながら嫌気的に混合攪拌されてメタ
ンガス生成する。このメタンガスは、回収されてエネル
ギーとして有効利用される。In the methane production tank, the acid production #, which has been decomposed mainly to acetic acid, is sent to the methane production tank, where it is heated at a predetermined temperature and y.
The mixture is mixed and stirred anaerobically while maintaining the pH at JZ to generate methane gas. This methane gas is recovered and effectively used as energy.
次に、メタン生成槽からの流出液は、後述の硝化槽から
の返送混合液及び沈殿槽からの返送汚泥と共に脱窒槽に
導ひかれ、イオウ細刻により、硝酸註窒素を微冗し、効
果的に脱窒処理する。ここにおけるイメウの添加は、前
述の嫌気性処■l′11工桿のうちの酸生成工程から発
生する硫化水素をその1ま通気することによって可能で
ある。場合(こよっては、この暁1ヒ水素をアルカリm
、’lV、に通して硫fヒナトリウムの形にして添U
O」するようにしてもよいし、不足のときは、他のイオ
ウあるいはイオウ化合物を添υ[jする。Next, the effluent from the methane generation tank is led to the denitrification tank together with the mixed liquid returned from the nitrification tank and the sludge returned from the settling tank, which will be described later. denitrification treatment. The addition of rice here is possible by bubbling hydrogen sulfide generated from the acid generation step in the anaerobic treatment tank 1'11 mentioned above. (In this case, this Akatsuki 1 arsenic is converted into an alkali m
, 'lV, and add it in the form of sulfuric acid.
Alternatively, if it is insufficient, other sulfur or sulfur compounds may be added.
脱窒槽からの混合液は、硝化槽に導ひかれ、ここでは好
気的に帆用(され、アンモニア11窒素は硝酸性窒素に
丑で硝化される。硝化された混合液の大部分は、前述の
脱窒槽に返送され、一部は沈殿槽て同液分離処理されて
上澄液は処理水として排出されるとともに、固形分の多
くは返送汚泥として、前述の脱窒槽へ送られる。The mixture from the denitrification tank is led to the nitrification tank, where it is aerobically nitrified, and the ammonia-11 nitrogen is nitrified to nitrate nitrogen. Most of the nitrified mixture is A portion of the sludge is returned to the denitrification tank, and a portion is separated in the sedimentation tank, and the supernatant liquid is discharged as treated water, while most of the solid content is sent as return sludge to the denitrification tank.
第2図の処理フローは、第1図の処理フローからメタン
生成!i!!!全省略した処理フローになっいる二)o
バクターのような従栄養性脱窒細菌をも利用して脱窒す
る。したがって、第1図の処理フローからメタン生成槽
の機能を除いた説明が、この処理フローの説明になるの
で、重複を避けるために省略する。しかし、なぜこの処
理フローが11能であるかは次の理由による。The process flow in Figure 2 is similar to the process flow in Figure 1 to generate methane! i! ! ! The process flow is completely omitted 2) o
Denitrification is also performed using eutrophic denitrifying bacteria such as Bacterium. Therefore, the explanation of this processing flow will be the same as the processing flow of FIG. 1 except for the function of the methane generation tank, so the description will be omitted to avoid duplication. However, the reason why this processing flow is eleven-fold is as follows.
つまり、11t来から行なわれている生物学的脱窒反応
は、従属栄養性の脱窒細菌を利−用し、このとき水素供
−り体として汚水中の有機物(BOL)Jや添IJII
したメタノール全利用する。この」弱行、汚水が下水
のときはBOD成分たけで脱窒できるのは、窒素成分の
6〜7割にすぎない。これに対し、第2図の処理フロー
では、酸生成槽で生成された有機酸を水素供与体として
利用することができるとともに、酸生成槽から発生する
硫化水素を脱窒槽に導くことによっても脱窒反応を促進
できる。また、この場合添加する硫化水素が少なくてす
むという利益もある。In other words, the biological denitrification reaction that has been carried out since 11th century uses heterotrophic denitrifying bacteria, and at this time, organic matter (BOL) in wastewater and additive IJII are used as hydrogen donors.
All of the methanol is used. In this case, when the wastewater is sewage, only 60 to 70% of the nitrogen content can be denitrified by the BOD content. On the other hand, in the process flow shown in Figure 2, the organic acid generated in the acid generation tank can be used as a hydrogen donor, and hydrogen sulfide generated from the acid generation tank can also be denitrified by leading it to the denitrification tank. Can promote nitrogen reaction. There is also the advantage that less hydrogen sulfide is added in this case.
以上、本発明によれば、汚水を嫌気性処理することによ
り、発生汚泥量が少ないばかりか、メタンガスとしての
エネルギー回収もb」能であり、また、嫌気性処理から
発生する硫化水素を廟効に利用して脱窒反応を可能とし
た、有用な発明ということができる。As described above, according to the present invention, by anaerobically treating wastewater, not only the amount of sludge generated is small, but also energy can be recovered as methane gas, and hydrogen sulfide generated from anaerobic treatment is effectively removed. It can be said that this is a useful invention that enables the denitrification reaction to be performed.
実施例
汚水として、牛し尿(BOD 1+、o o omqB
、アンモニア性窒素3.50 omq/、e ) k、
第・2図の処理フローで処理した。As the example wastewater, cow human waste (BOD 1+, o o omqB
, ammonia nitrogen 3.50 omq/, e) k,
It was processed using the processing flow shown in Figure 2.
酸生成槽(有効容積201)に投入し、温度20 C,
()’H6,5〜7.5に調整しながら滞留時間10日
の条件で酸生成反応を行った。Pour into the acid generation tank (effective volume 201) and set the temperature to 20 C.
()' The acid production reaction was carried out under the conditions of residence time of 10 days while adjusting the H6.5 to 7.5.
次きに、酸生成液1にiJ L、4倍量の硝化槽からの
返送混合液と10倍量の返送汚泥と共に脱窒槽に導ひい
て嫌気的に混合攪拌を行い、滞留時間()5日の条件で
脱窒処理した。ここで酸生成槽から発生した硫化水素を
硝酸性窒素1モルに7・1シ、イAつとして1モルの割
合で添加した。Next, the acid production liquid 1 was introduced into the denitrification tank together with iJ L, 4 times the amount of the returned mixed liquid from the nitrification tank, and 10 times the amount of the returned sludge, and mixed and stirred anaerobically, and the residence time () 5 Denitrification treatment was carried out under the conditions of 1 day. Here, hydrogen sulfide generated from the acid generation tank was added at a ratio of 7.1 mol to 1 mol of nitrate nitrogen.
脱窒槽からの混合液は、次の硝化槽で好気的に処理され
て、硝化率98%で処理し、前述のように硝化液の一部
は脱窒槽へ、残部は沈殿槽を介して処理水として排出し
た。The mixed liquid from the denitrification tank is aerobically treated in the next nitrification tank to achieve a nitrification rate of 98%, and as mentioned above, part of the nitrification liquid goes to the denitrification tank and the rest goes through the settling tank. Discharged as treated water.
このときの処理7.K 水質は、B OD 30t++
!//−Q 。Processing at this time 7. K Water quality is B OD 30t++
! //-Q.
T−N8m9/13であった。It was T-N8m9/13.
なお、脱窒槽に酸生成槽からの硫化水素を添−加しなか
った場合は、処理水中の801)は変らなかったが、T
−Ns4.amり/−eと高い値を示した。Note that when hydrogen sulfide from the acid generation tank was not added to the denitrification tank, 801) in the treated water did not change, but T
-Ns4. It showed a high value of amri/-e.
す、上のように、本発明によれば、効果的に汚水中から
アンモニア性窒素を除去することができる。As described above, according to the present invention, ammonia nitrogen can be effectively removed from wastewater.
第1図及び第2図(は、本発明を実施するのに好適な処
理フロー1示す。
特訂出顆人 松 井 三 部
〃 栗田工業株式会社Figures 1 and 2 (show a processing flow 1 suitable for carrying out the present invention).
Claims (1)
いで硝化脱窒工程で処理する工程からなり、嫌気性処理
工程で発生する硫化水素を硝化脱窒処理の自栄養細菌を
利用して脱窒する脱窒槽へ供給することを特徴とする窒
素成分を含む汚水の処理方法。 2 嫌気性処理工程は、酸生成反応及びメタン生成反応
の二相式嫌気処理である特許請求の範囲第1項記載の窒
素成分を含む汚水の処理方法。 3 嫌気性処理工程は、酸生成反応処理である特、i/
[請求の範囲第1項記載の窒素成分を含むlPJボの処
理方法。[Claims] l Consisting of a process in which wastewater containing nitrogen components is treated in an anaerobic treatment process and then in a nitrification-denitrification process, and the hydrogen sulfide generated in the anaerobic treatment process is converted into an autotrophic nutrient during the nitrification-denitrification process. A method for treating wastewater containing nitrogen components, characterized by supplying wastewater to a denitrification tank that denitrifies using bacteria. 2. The method for treating wastewater containing nitrogen components according to claim 1, wherein the anaerobic treatment step is a two-phase anaerobic treatment of an acid production reaction and a methane production reaction. 3 The anaerobic treatment step is an acid production reaction treatment, i/
[A method for treating IPJ water containing a nitrogen component as set forth in claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14043282A JPS603876B2 (en) | 1982-08-12 | 1982-08-12 | Method for treating wastewater containing nitrogen components |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14043282A JPS603876B2 (en) | 1982-08-12 | 1982-08-12 | Method for treating wastewater containing nitrogen components |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5929092A true JPS5929092A (en) | 1984-02-16 |
| JPS603876B2 JPS603876B2 (en) | 1985-01-31 |
Family
ID=15268532
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14043282A Expired JPS603876B2 (en) | 1982-08-12 | 1982-08-12 | Method for treating wastewater containing nitrogen components |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS603876B2 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4839052A (en) * | 1987-03-10 | 1989-06-13 | Council For Scientific And Industrial Research | Biological treatment of water |
| JPH0699189A (en) * | 1992-01-18 | 1994-04-12 | Hitachi Plant Eng & Constr Co Ltd | Removing method for nitrogen in waste water |
| JP2005279405A (en) * | 2004-03-29 | 2005-10-13 | Cosmo Oil Co Ltd | Method for removing nitrogen in wastewater |
| JP2005288371A (en) * | 2004-04-01 | 2005-10-20 | Sumitomo Heavy Ind Ltd | Wastewater treatment method |
| US7109022B1 (en) | 1998-09-25 | 2006-09-19 | Nitchitsu Co., Ltd | Composition containing calcium carbonate particles dispersed in sulfur for removing nitrate nitrogen |
| JP2014233691A (en) * | 2013-06-04 | 2014-12-15 | 株式会社東芝 | Wastewater treatment apparatus |
-
1982
- 1982-08-12 JP JP14043282A patent/JPS603876B2/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4839052A (en) * | 1987-03-10 | 1989-06-13 | Council For Scientific And Industrial Research | Biological treatment of water |
| JPH0699189A (en) * | 1992-01-18 | 1994-04-12 | Hitachi Plant Eng & Constr Co Ltd | Removing method for nitrogen in waste water |
| US7109022B1 (en) | 1998-09-25 | 2006-09-19 | Nitchitsu Co., Ltd | Composition containing calcium carbonate particles dispersed in sulfur for removing nitrate nitrogen |
| JP2005279405A (en) * | 2004-03-29 | 2005-10-13 | Cosmo Oil Co Ltd | Method for removing nitrogen in wastewater |
| JP2005288371A (en) * | 2004-04-01 | 2005-10-20 | Sumitomo Heavy Ind Ltd | Wastewater treatment method |
| JP2014233691A (en) * | 2013-06-04 | 2014-12-15 | 株式会社東芝 | Wastewater treatment apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS603876B2 (en) | 1985-01-31 |
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