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JP2002361300A - Sludge treatment method - Google Patents

Sludge treatment method

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Publication number
JP2002361300A
JP2002361300A JP2001175532A JP2001175532A JP2002361300A JP 2002361300 A JP2002361300 A JP 2002361300A JP 2001175532 A JP2001175532 A JP 2001175532A JP 2001175532 A JP2001175532 A JP 2001175532A JP 2002361300 A JP2002361300 A JP 2002361300A
Authority
JP
Japan
Prior art keywords
sludge
nitrite
added
concentration
concentrated
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
JP2001175532A
Other languages
Japanese (ja)
Other versions
JP3900511B2 (en
Inventor
Yasuhiro Oi
康裕 大井
Yasuhiro Mugibayashi
裕弘 麦林
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.)
Kurita Water Industries Ltd
Original Assignee
Kurita Water Industries 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 Kurita Water Industries Ltd filed Critical Kurita Water Industries Ltd
Priority to JP2001175532A priority Critical patent/JP3900511B2/en
Publication of JP2002361300A publication Critical patent/JP2002361300A/en
Application granted granted Critical
Publication of JP3900511B2 publication Critical patent/JP3900511B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Treatment Of Sludge (AREA)

Abstract

(57)【要約】 【課題】濃縮工程での汚泥浮上と臭気発生を防止すると
共に、以降の工程の臭気発生を抑制し、かつ最終工程の
汚泥の脱水性を向上させることのできる汚泥処理方法を
提供する。 【解決手段】余剰汚泥を含有する最初沈澱池引抜き汚泥
の処理方法であって、該引抜き汚泥に亜硝酸塩を、亜硝
酸イオンが10〜50mg/L対汚泥容量となるように添
加し、pH6未満にて該汚泥を重力濃縮する、あるいは余
剰汚泥を含有しない最初沈澱池引抜き汚泥の処理方法で
あって、該引抜き汚泥に亜硝酸塩を添加し、該汚泥を重
力濃縮する。
(57) [Solution] A sludge treatment method capable of preventing sludge floating and odor generation in a concentration step, suppressing odor generation in a subsequent step, and improving sludge dewaterability in a final step. I will provide a. A method for treating sludge from a primary sedimentation basin containing excess sludge, wherein nitrite is added to the sludge from the sludge so that nitrite ions have a volume of 10 to 50 mg / L per sludge volume, and the pH is less than 6 In which the sludge is gravity-concentrated, or a method for treating sludge from the initial settling basin that does not contain excess sludge, wherein nitrite is added to the sludge and the gravity is concentrated.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は汚泥処理方法に関す
る。さらに詳しくは、本発明は、余剰汚泥を含有する最
初沈澱池引抜き汚泥及び余剰汚泥を含有しない最初沈澱
池引抜き汚泥を、亜硝酸塩の存在下で重力濃縮を行い、
濃縮工程から発生する臭気を防止すると共に、以降の工
程の臭気発生を抑制し、かつ最終工程の汚泥の脱水性を
向上させることのできる汚泥処理方法に関するものであ
る。
[0001] The present invention relates to a method for treating sludge. More specifically, the present invention provides that the first settling tank drawn sludge containing excess sludge and the first settling tank drawn sludge containing no excess sludge are subjected to gravity concentration in the presence of nitrite,
The present invention relates to a sludge treatment method capable of preventing odor generated from a concentration step, suppressing odor generation in a subsequent step, and improving sludge dewatering property in a final step.

【0002】[0002]

【従来の技術】従来、下水処理工程における最初沈澱池
から発生する汚泥は、通常重力濃縮工程を経て脱水処理
されている。しかしながら、この重力濃縮槽において
は、例えば(1)汚泥濃縮不良、(2)汚泥浮上による
濃縮槽越流水への汚濁物質の流出、(3)上記(1)及
び(2)による汚泥脱水性の悪化、(4)硫化水素、メ
チルメルカプタンに代表される悪臭の発生、(5)揮散
した硫化水素が生物化学的に酸化されて生じる硫酸によ
る濃縮槽自体や付帯機器の腐食、など数多くの問題があ
る。したがって、このような問題に対処するために、例
えば臭気については、濃縮槽を覆蓋して、臭気を別途処
理するなどの対策が講ぜられており、汚泥の濃度低下や
脱水性悪化については、脱水薬剤の開発検討、脱水機の
効率向上検討などが行われている。また、濃縮槽越流水
に流出する固形物対策としては、最初沈澱池に汚泥を貯
めないようにする、濃縮槽内の汚泥ゾーンを低く保つな
どの運転管理の推進が図られている。しかしながら、こ
れらの対策では、十分に満足すべき結果が得られていな
いのが実状である。ところで、汚泥の重力濃縮槽におけ
る前述の現象そのものをなくす手段、あるいは薬剤処理
における薬剤軽減化に関する手段としては、過酸化水
素、亜塩素酸ナトリウム、次亜塩素酸ナトリウムなどの
酸化剤が、重力濃縮槽における汚泥浮上の防止や、臭気
防止に有効であることが報告されている。しかしなが
ら、例えば過酸化水素については、分解酸素ガスでの浮
上があるため、薬剤添加後に曝気による脱気処理を行う
必要があり、この場合、装置が大がかりなものになるの
を免れない上、管理が難しいなどの問題が生じる。ま
た、亜塩素酸ナトリウムや次亜塩素酸ナトリウムについ
ても、その添加費用に見合う満足する効果は得られず、
ほとんど実用化されていない。一方、亜硝酸塩は、汚泥
中の微生物活動を抑制して硫化水素の発生を防止する効
果、及びゆっくりではあるが、すでに発生している硫化
水素の分解効果を発揮することが知られている。しかし
ながら、特開昭56−38196号公報では、汚泥に亜
硝酸塩を添加して浮上濃縮する技術が開示されているよ
うに、あるいは「活性汚泥のバルキングと生物発泡の制
御」(Jiri Wanner著、河野哲朗他訳、技報
堂出版、第103ページ)では、亜硝酸塩と同様に生物
学的脱窒素が起こる硝酸塩について、6〜8mg/Lの硝
酸性窒素の存在は、活性汚泥処理における最終沈澱池で
汚泥を浮上させる、という記述があるように、亜硝酸イ
オン及び硝酸イオンは、汚泥の重力沈降及び汚泥の重力
濃縮では、好ましくない物質、できれば忌避すべき物質
であることが、これまで常識であった。汚泥処理におい
て、亜硝酸塩を用いた技術としては、例えば特開200
0−202494号公報、特開2000−288592
号公報、特開2000−351000号公報に、亜硝酸
塩を汚泥濃縮槽に添加して脱水ケーキを消臭することが
開示されている。しかしながら、これらの技術は、いず
れも脱水ケーキの臭気発生防止に関するものであって、
汚泥を重力濃縮する旨の記載がなく、また、余剰汚泥を
含有しており、さらに、亜硝酸イオンの添加量として、
50mg/L以下に設定する旨の記載もない。また、特開
2000−185290号公報には、濃縮槽などに亜硝
酸塩を添加することが記載されている。しかしながら、
この技術は、過酸化水素を併用するものであり、本発明
とは異なる。
2. Description of the Related Art Conventionally, sludge generated from a first settling pond in a sewage treatment process is usually subjected to a dewatering treatment through a gravity concentration process. However, in this gravity concentration tank, for example, (1) poor sludge concentration, (2) outflow of pollutants into overflow of the concentration tank due to sludge floating, and (3) sludge dewatering property by the above (1) and (2). Deterioration, (4) generation of foul odors typified by hydrogen sulfide and methyl mercaptan, and (5) corrosion of the enrichment tank itself and incidental equipment due to sulfuric acid generated by the biochemical oxidation of volatilized hydrogen sulfide. is there. Therefore, in order to deal with such a problem, for example, for the odor, measures such as covering the concentration tank and separately treating the odor have been taken. Studies are being conducted on the development of chemicals and on the efficiency of dehydrators. In addition, as a measure against solids flowing into the overflow of the thickening tank, the promotion of operation management such as preventing sludge from being initially stored in the sedimentation basin and keeping the sludge zone in the thickening tank low is being promoted. However, these measures have not been able to provide satisfactory results. By the way, as a means to eliminate the above-mentioned phenomenon itself in the gravity concentration tank of sludge or to reduce the chemical in the chemical treatment, oxidizing agents such as hydrogen peroxide, sodium chlorite, and sodium hypochlorite are concentrated by gravity. It is reported that it is effective in preventing sludge floating in the tank and odor. However, for example, since hydrogen peroxide floats with decomposed oxygen gas, it is necessary to perform a deaeration treatment by aeration after adding a chemical, and in this case, it is unavoidable that the apparatus becomes large-scale and control Problems such as difficulties arise. Also, with respect to sodium chlorite and sodium hypochlorite, a satisfactory effect commensurate with the addition cost cannot be obtained,
It has hardly been put to practical use. On the other hand, it is known that nitrite exerts the effect of suppressing the microbial activity in sludge to prevent the generation of hydrogen sulfide and the effect of decomposing hydrogen sulfide, which has already been generated, albeit slowly. However, Japanese Patent Application Laid-Open No. S56-38196 discloses a technique of adding nitrite to a sludge to float and concentrate, or "Control of bulking and biological foaming of activated sludge" (by Jiri Wanner, Kono According to Tetsuro et al., Gihodo Shuppan, p. 103), for nitrate, which causes biological denitrification as well as nitrite, the presence of 6-8 mg / L nitrate nitrogen in the final settling tank in activated sludge treatment It has been common knowledge that nitrite ions and nitrate ions are undesired substances, preferably substances that should be avoided in gravity sedimentation of sludge and gravity concentration of sludge. . In the sludge treatment, a technique using nitrite is disclosed in, for example, JP-A-200
0-202494, JP-A-2000-288592
JP-A-2000-351000 discloses that nitrite is added to a sludge concentration tank to deodorize a dehydrated cake. However, these techniques are all related to prevention of odor generation of the dehydrated cake,
There is no statement that the sludge is concentrated by gravity, and it also contains excess sludge.
There is no description to set the dose to 50 mg / L or less. Japanese Patent Application Laid-Open No. 2000-185290 describes that nitrite is added to a concentration tank or the like. However,
This technique uses hydrogen peroxide in combination and is different from the present invention.

【0003】[0003]

【発明が解決しようとする課題】本発明は、前述したよ
うな従来の汚泥処理における重力濃縮槽での問題を解決
し、濃縮工程から発生する臭気を防止すると共に、以降
の工程の臭気発生を抑制し、かつ最終工程の汚泥の脱水
性を向上させることのできる汚泥処理方法を提供するこ
とを目的としてなされたものである。
SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems in the conventional gravity sludge tank in sludge treatment, prevents odor generated from the concentration step, and reduces odor generation in the subsequent steps. It is an object of the present invention to provide a sludge treatment method capable of suppressing and improving the sludge dewatering property in the final step.

【0004】[0004]

【課題を解決するための手段】本発明者らは、前記目的
を達成するために、汚泥消臭剤として適用されている亜
硝酸塩に着目し、その使用条件などについて詳細に検討
を重ねた結果、最初沈澱池引抜き汚泥に対し、亜硝酸イ
オン量がある範囲になるように亜硝酸塩を添加して、該
汚泥を重力濃縮することにより、意外にも汚泥浮上が促
進されることがない(悪影響がない)にとどまらず、浮
上時間が格段に無処理より延長する、すなわち亜硝酸塩
が従来の常識に反して、顕著な浮上防止効果を発揮する
ことができ、前記目的を達成し得ることを見出し、この
知見に基づいて本発明を完成するに至った。すなわち、
本発明は、(1)余剰汚泥を含有する最初沈澱池引抜き
汚泥の処理方法であって、該引抜き汚泥に亜硝酸塩を、
亜硝酸イオンが10〜50mg/L対汚泥容量となるよう
に添加し、pH6未満にて該汚泥を重力濃縮することを特
徴とする汚泥処理方法、(2)余剰汚泥を含有しない最
初沈澱池引抜き汚泥の処理方法であって、該引抜き汚泥
に亜硝酸塩を添加し、該汚泥を重力濃縮することを特徴
とする汚泥処理方法、(3)亜硝酸塩を、亜硝酸イオン
が10〜70mg/L対汚泥容量となるように添加する第
2項記載の汚泥処理方法、(4)引抜き汚泥を希釈する
第1項、第2項又は第3項記載の汚泥処理方法、(5)
引抜き汚泥に酸性物質を添加する第1項ないし第4項の
いずれかに記載の汚泥処理方法、及び(6)重力濃縮後
の汚泥を貯留する汚泥貯留槽に亜硝酸塩を添加する第1
項ないし第5項のいずれかに記載の汚泥処理方法、を提
供するものである。
Means for Solving the Problems In order to achieve the above object, the present inventors have focused on nitrite which has been applied as a sludge deodorant, and have conducted detailed studies on its use conditions and the like. By adding nitrite so that the amount of nitrite ions is within a certain range to the sludge initially drawn from the sedimentation basin and concentrating the sludge by gravity, the floating of the sludge is not unexpectedly promoted (adverse effect). Not found), the ascent time is much longer than that of no treatment, that is, nitrite can exert a remarkable anti-floating effect, contrary to the conventional wisdom, and can achieve the above object. The present invention has been completed based on this finding. That is,
The present invention relates to (1) a method for treating sludge drawn from a first sedimentation basin containing excess sludge, wherein nitrite is added to the drawn sludge;
A method for treating sludge, characterized by adding nitrite ions in an amount of 10 to 50 mg / L with respect to sludge volume, and subjecting the sludge to gravity concentration at a pH of less than 6, (2) withdrawing a first sedimentation basin containing no excess sludge A method for treating sludge, wherein nitrite is added to the extracted sludge and the sludge is concentrated by gravity. (3) A method for treating nitrite, wherein nitrite is contained in an amount of 10 to 70 mg / L relative to nitrite. The sludge treatment method according to Item 2, wherein the sludge treatment method is added so as to have a sludge capacity; (4) The sludge treatment method according to Item 1, 2, or 3 for diluting drawn sludge; (5)
The sludge treatment method according to any one of items 1 to 4, wherein an acidic substance is added to the drawn sludge, and (6) a method in which nitrite is added to a sludge storage tank for storing sludge after gravity concentration.
A method for treating sludge according to any one of Items 5 to 5.

【0005】[0005]

【発明の実施の形態】本発明の汚泥処理方法は、(1)
余剰汚泥を含有する最初沈澱池引抜き汚泥を処理する方
法と、(2)余剰汚泥を含有しない最初沈澱池引抜き汚
泥を処理する方法の2つの態様がある。本発明の汚泥処
理方法においては、余剰汚泥を含有する最初沈澱池引抜
き汚泥(以下、初沈引抜き汚泥と略称することがある)
又は余剰汚泥を含有しない初沈引抜き汚泥に対して、亜
硝酸塩を添加し、該汚泥を重力濃縮する。前記亜硝酸塩
の添加量が多すぎると、亜硝酸の分解が速やかに生じた
場合に、急激に窒素ガスが生じ、その結果汚泥が浮上し
て濃縮が困難となる。特に余剰汚泥を含有する初沈引抜
き汚泥においてこの傾向が顕著になる。これは、余剰汚
泥が亜硝酸イオンを消費する微生物(亜硝酸還元菌な
ど)を多量に含んでいるためである。したがって、余剰
汚泥を含有する初沈引抜き汚泥に対しては、亜硝酸塩の
添加量は、亜硝酸イオンとして50mg/L対汚泥容量以
下にすることが必要である。亜硝酸イオン量が50mg/
L対汚泥容量を超えると汚泥の浮上が生じて濃縮が困難
となり、本発明の目的が達せられない。また、亜硝酸塩
の添加量の下限は、亜硝酸イオンとして10mg/L対汚
泥容量である。亜硝酸イオン量が10mg/L対汚泥容量
未満では臭気発生防止や炭酸ガス発生抑制による浮上防
止、あるいは腐敗防止の効果が十分に発揮されず、本発
明の目的が達せられない。好ましい亜硝酸塩の添加量
は、亜硝酸イオンとして15〜45mg/L対汚泥容量の
範囲で選定される。一方、余剰汚泥を含まない初沈引抜
き汚泥の場合には、亜硝酸イオンの消費速度が遅いた
め、前記の余剰汚泥が混合されている場合に比較して、
多量の亜硝酸塩を添加しても窒素ガスが急激に発生せ
ず、汚泥が浮上しにくい。そして、窒素ガスによる汚泥
浮上が生じない亜硝酸塩の添加量の上限は、処理場によ
って異なる。したがって、亜硝酸塩の添加量としては特
に制限はないが、経済性や安全性、効果などを考慮し
て、一般的には、硝酸イオンとして、10〜70mg/L
対汚泥容量であり、好ましくは15〜45mg/Lの範囲
で選定される。また、汚泥濃度が高い場合、臭気発生防
止、炭酸ガス生成の抑制、腐敗防止に必要な亜硝酸塩の
必要添加量は増大する。しかし、上述したように、一方
で亜硝酸塩の添加量が増大すると、窒素ガスの発生量が
多くなり、その結果汚泥が浮上する危険性が増大する。
したがって、汚泥濃度が高い場合には、汚泥を希釈する
ことが好ましい。濃縮前の引抜き汚泥の濃度は、200
00mg/L未満、特に8000〜15000mg/Lの範
囲に調整するのが有利である。引抜き汚泥の濃度が低す
ぎると、濃縮槽の容量に対して水面積負荷が過大となり
好ましくない。この希釈には、流入下水や最初沈澱池越
流水などを使用することができる。
BEST MODE FOR CARRYING OUT THE INVENTION The sludge treatment method of the present invention comprises (1)
There are two modes, a method of treating the first settling tank drawn sludge containing excess sludge, and a method of treating (2) the first settling tank drawn sludge not containing excess sludge. In the sludge treatment method of the present invention, first settling tank drawn sludge containing excess sludge (hereinafter, may be abbreviated as first settled sludge).
Alternatively, nitrite is added to the initial settled sludge containing no excess sludge, and the sludge is gravity-concentrated. If the amount of the nitrite is too large, when the decomposition of nitrous acid occurs promptly, nitrogen gas is rapidly generated, and as a result, sludge floats and concentration becomes difficult. In particular, this tendency becomes remarkable in the initial settling sludge containing excess sludge. This is because excess sludge contains a large amount of microorganisms (such as nitrite-reducing bacteria) that consume nitrite ions. Therefore, the amount of nitrite to be added to the initial settled sludge containing surplus sludge must be 50 mg / L as nitrite ion or less per sludge volume. Nitrite ion content is 50mg /
When the volume exceeds L, the sludge floats and the concentration becomes difficult, and the object of the present invention cannot be achieved. The lower limit of the amount of nitrite added is 10 mg / L as nitrite ion per sludge volume. If the amount of nitrite ions is less than 10 mg / L per sludge volume, the effects of preventing odor generation, floating prevention by suppressing carbon dioxide gas generation, and preventing rot are not sufficiently exhibited, and the object of the present invention cannot be achieved. The preferred amount of nitrite added is selected in the range of 15-45 mg / L as nitrite ion per sludge volume. On the other hand, in the case of the initial settling sludge that does not contain excess sludge, the consumption rate of nitrite ions is slow, so that compared to the case where the excess sludge is mixed,
Even if a large amount of nitrite is added, nitrogen gas is not rapidly generated, and sludge hardly floats. The upper limit of the amount of nitrite that does not cause sludge floating by nitrogen gas varies depending on the treatment plant. Therefore, the amount of the nitrite added is not particularly limited, but is generally 10 to 70 mg / L as nitrate ion in consideration of economy, safety, effects, and the like.
It is the sludge capacity, and is preferably selected in the range of 15 to 45 mg / L. When the sludge concentration is high, the required amount of nitrite added for preventing odor generation, suppressing carbon dioxide gas generation, and preventing rot increases. However, as described above, on the other hand, when the amount of addition of nitrite increases, the amount of generated nitrogen gas increases, and as a result, the risk of sludge floating increases.
Therefore, when the sludge concentration is high, it is preferable to dilute the sludge. The concentration of the extracted sludge before concentration is 200
It is advantageous to adjust it to less than 00 mg / L, in particular in the range from 8000 to 15000 mg / L. If the concentration of the drawn sludge is too low, the water area load is excessively large with respect to the capacity of the concentration tank, which is not preferable. For this dilution, inflow sewage or first settling pond overflow water can be used.

【0006】また、新設の処理場や、既設処理場でも、
汚泥処理フローを改善する場合には、初沈引抜き汚泥及
び余剰汚泥は、それぞれ濃縮処理された後に混合される
ことがある。そしてこの場合、初沈引抜き汚泥の濃度が
高くなるため、汚泥容量当たりの必要亜硝酸イオン量が
増大することから、上述のように、初沈引抜き汚泥を希
釈することは、特に余剰汚泥を含有しない汚泥に対して
有効である。本発明の汚泥処理においては、汚泥は、余
剰汚泥を含有する場合には、pH6未満で重力濃縮され、
余剰汚泥を含有しない場合にもpH6未満で重力濃縮する
ことが好ましいものの、本発明が適用できるpHは汚泥性
状によって異なる。そして、余剰汚泥の含有の有無に関
係なく、特にpH4.5〜5.5の範囲に調整するのが好ま
しい。このようにpHを調整することにより、亜硝酸の分
解、消失速度が軽減され、亜硝酸の効果が少量で持続す
ると同時に、急激に窒素ガスが発生しなくなるため、窒
素ガスによる汚泥浮上も生じにくくなる。このpHが低す
ぎるとpH依存性の効果が低くなる上、装置の腐食の問題
及び二酸化炭素ガスの飽和濃度が低くなることにより、
炭酸ガスが発生しやすくなる。このpH調整には、例えば
硫酸や塩酸などの鉱酸、硫酸第一鉄、塩化第二鉄、塩化
第一鉄などの中から選ばれる少なくとも1種の酸性物質
を使用することができるが、後工程での硫化水素の発生
のもとになる硫酸根を含まないものが好ましい。また、
鉄塩はリンを固定し、水処理に返流する濃縮分解水のリ
ンを低減させ、最終的に処理水のリン濃度を削減できる
ことから好ましい。したがって、特に第二鉄塩を使用す
ることが好ましい。従来の施設では、余剰汚泥は最初沈
澱池あるいはその前段に返送されることが多く、初沈引
抜き汚泥は余剰汚泥と共に濃縮される。このような場
合、汚泥濃度は薄いものの、亜硝酸イオンを消費する微
生物(亜硝酸還元菌など)を多量に含んでいる。したが
って、前記の酸性物質の添加によるpH調整は、特に余剰
汚泥を含有する引抜き汚泥に対して有効である。さら
に、本発明においては、重力濃縮後の汚泥を貯留する汚
泥貯留槽に亜硝酸塩を添加することにより、汚泥処理工
程全体での臭気発生を効果的に防止することができる。
すなわち、初沈引抜き汚泥に亜硝酸塩を添加し、重力濃
縮することにより、重力濃縮槽での臭気発生を防止する
ことができるが、該貯留槽、汚泥脱水工程、脱水ケーキ
での臭気発生を完全には防止することは困難である。し
たがって、該貯留槽に亜硝酸塩を添加することによっ
て、汚泥処理工程全体での臭気発生を防止することが可
能となる。本発明の汚泥処理方法において添加する亜硝
酸塩としては、水溶性のものであればよく、特に制限は
ないが、経済性などの面から、亜硝酸ナトリウムや亜硝
酸カルシウムなどを好適に使用することができる。亜硝
酸亜鉛は、毒性などの点で好ましくない。前記亜硝酸塩
は1種用いてもよいし、2種以上を組み合わせて用いて
もよい。また、本発明においては、特開2000−28
8592号公報及び特開2000−351000号公報
において、亜硝酸塩と併用した硝酸塩などの金属塩や有
機系殺菌剤ソルビン酸などを亜硝酸塩と共に併用するこ
とができる。図1及び図2は、それぞれ本発明におけ
る、余剰汚泥を含有する最初沈澱池引抜き汚泥及び余剰
汚泥を含有しない最初沈澱池引抜き汚泥の処理方法の1
例を示す工程系統図である。
[0006] In addition, even in a new treatment plant or an existing treatment plant,
When improving the sludge treatment flow, the initial settled sludge and the excess sludge may be mixed after being concentrated respectively. And in this case, since the concentration of the initial settled sludge is increased, the required amount of nitrite ion per sludge volume is increased. Therefore, as described above, diluting the initial settled sludge includes, in particular, excess sludge. Not effective against sludge. In the sludge treatment of the present invention, when excess sludge is contained, the sludge is concentrated by gravity at a pH of less than 6,
Even when excess sludge is not contained, it is preferable to carry out gravity concentration at a pH lower than 6, but the pH to which the present invention can be applied differs depending on the sludge properties. It is particularly preferable to adjust the pH to a range of 4.5 to 5.5 regardless of the presence or absence of excess sludge. By adjusting the pH in this manner, the rate of decomposition and disappearance of nitrous acid is reduced, and the effect of nitrous acid is maintained in a small amount.At the same time, nitrogen gas is not generated suddenly, so that sludge floating by nitrogen gas hardly occurs. Become. If this pH is too low, the pH-dependent effect will be reduced, and the corrosion of the device and the saturated concentration of carbon dioxide gas will be reduced,
Carbon dioxide gas is easily generated. For this pH adjustment, for example, at least one acidic substance selected from mineral acids such as sulfuric acid and hydrochloric acid, ferrous sulfate, ferric chloride, and ferrous chloride can be used. Those which do not contain a sulfate group that causes generation of hydrogen sulfide in the process are preferable. Also,
Iron salts are preferred because they fix phosphorus, reduce the concentration of decomposed water returned to the water treatment, and ultimately reduce the phosphorus concentration in the treated water. Therefore, it is particularly preferable to use a ferric salt. In conventional facilities, surplus sludge is often returned to the sedimentation basin or the preceding stage, and the initial settled sludge is concentrated together with the surplus sludge. In such a case, although the sludge concentration is low, it contains a large amount of microorganisms (such as nitrite-reducing bacteria) that consume nitrite ions. Therefore, the pH adjustment by the addition of the acidic substance is particularly effective for drawn sludge containing excess sludge. Furthermore, in the present invention, the addition of nitrite to a sludge storage tank for storing sludge after gravity concentration can effectively prevent odor generation in the entire sludge treatment process.
That is, by adding nitrite to the initial settled sludge and performing gravity concentration, odor generation in the gravity concentration tank can be prevented, but odor generation in the storage tank, the sludge dewatering step, and the dewatered cake is completely prevented. It is difficult to prevent. Therefore, by adding nitrite to the storage tank, it becomes possible to prevent odor generation in the entire sludge treatment process. The nitrite to be added in the sludge treatment method of the present invention is not particularly limited as long as it is a water-soluble one, but it is preferable to use sodium nitrite or calcium nitrite from the viewpoint of economy and the like. Can be. Zinc nitrite is not preferred in terms of toxicity and the like. The nitrites may be used alone or in combination of two or more. Also, in the present invention, JP-A-2000-28
In JP-A-8592 and JP-A-2000-351000, a metal salt such as nitrate used in combination with nitrite, an organic fungicide sorbic acid, and the like can be used in combination with nitrite. FIG. 1 and FIG. 2 each show a method of treating the first settling tank drawn sludge containing excess sludge and the first settling tank drawn sludge not containing excess sludge in the present invention.
It is a process flow chart showing an example.

【0007】図1の工程系統図においては、下水などの
原水は最終沈澱池3からの余剰汚泥と共に、最初沈澱池
1に供給され汚泥が分離される。最初沈澱池1から引抜
かれた汚泥は、亜硝酸塩A又はBが添加され、重力濃縮
槽4において濃縮されたのち、濃縮汚泥として汚泥貯留
槽5に貯留される。この汚泥貯留槽5には、必要により
亜硝酸塩Cが添加され、濃縮汚泥は脱水機6により脱水
され、脱水ケーキとして排出される。一方、最初沈澱池
1からの上澄み液は、活性汚泥槽2を通って最終沈澱池
3に導かれ、汚泥が分離される。分離された汚泥は、一
部が返送汚泥として、活性汚泥槽2へ返送されると共
に、残余は余剰汚泥として最初沈澱池1へ移送される。
最終沈澱池3の上澄み液は、そのままで、又は必要な処
理が施されたのち、放流される。図2の工程系統図にお
いては、下水などの原水は最初沈澱池1に供給され、汚
泥が分離される。最初沈澱池1から引抜かれた汚泥は、
亜硝酸塩A又はBが添加され、重力濃縮槽4において濃
縮される。最初沈澱池1からの上澄み液は、活性汚泥槽
2を通って最終沈澱池3に導かれ、汚泥が分離される。
分離された汚泥は、一部が返送汚泥として、活性汚泥槽
2へ返送されると共に、残余は、遠心濃縮機7などによ
り濃縮されたのち、余剰濃縮汚泥として、前記の重力濃
縮槽4からの濃縮汚泥と共に汚泥貯留槽5に貯留され
る。この汚泥貯留槽5には、必要により亜硝酸塩Cが添
加され、混合濃縮汚泥は脱水機6により脱水され、脱水
ケーキとして排出される。最終沈澱池3の上澄み液は、
そのままで、又は必要な処理が施されたのち、放流され
る。前記脱水機6としては、例えば遠心脱水機、ベルト
プレス脱水機、スクリュープレス脱水機、フィルタープ
レス脱水機、真空脱水機などを用いることができる。
In the process flow diagram of FIG. 1, raw water such as sewage is first supplied to the sedimentation basin 1 together with excess sludge from the final sedimentation basin 3 to separate sludge. The sludge initially drawn from the sedimentation basin 1 is added with nitrite A or B, concentrated in the gravity concentration tank 4, and then stored in the sludge storage tank 5 as concentrated sludge. If necessary, nitrite C is added to the sludge storage tank 5, and the concentrated sludge is dewatered by the dehydrator 6 and discharged as a dewatered cake. On the other hand, the supernatant liquid from the first settling basin 1 is first passed through the activated sludge tank 2 to the final settling basin 3, where the sludge is separated. Part of the separated sludge is returned to the activated sludge tank 2 as return sludge, and the remainder is first transferred to the sedimentation basin 1 as excess sludge.
The supernatant liquid of the final sedimentation basin 3 is discharged as it is or after being subjected to necessary treatment. In the process flow diagram of FIG. 2, raw water such as sewage is first supplied to the sedimentation basin 1 and sludge is separated. First, the sludge extracted from the sedimentation basin 1
The nitrite A or B is added and concentrated in the gravity concentration tank 4. First, the supernatant liquid from the sedimentation basin 1 is led to the final sedimentation basin 3 through the activated sludge tank 2 where sludge is separated.
A part of the separated sludge is returned to the activated sludge tank 2 as a part of returned sludge, and the remainder is concentrated by a centrifugal concentrator 7 or the like. It is stored in the sludge storage tank 5 together with the concentrated sludge. If necessary, nitrite C is added to the sludge storage tank 5, and the mixed concentrated sludge is dewatered by the dehydrator 6 and discharged as a dewatered cake. The supernatant of the final settling basin 3 is
It is discharged as it is or after necessary processing has been performed. Examples of the dehydrator 6 include a centrifugal dehydrator, a belt press dehydrator, a screw press dehydrator, a filter press dehydrator, and a vacuum dehydrator.

【0008】[0008]

【実施例】次に、本発明を実施例により、さらに詳細に
説明するが、本発明は、これらの例によってなんら限定
されるものではない。なお、実施例及び比較例におい
て、硫化水素の分析は、ガス検知管[ガステック4M、
4L又は4LL]を用い、メチルメルカプタンの分析
は、ガス検知管[ガステック71H又は71]を用いて
行った。検出下限濃度は、硫化水素、メチルメルカプタ
ン共に1ppmである。 実施例1〜3及び比較例1〜3 余剰汚泥を含有する最初沈澱池引抜き汚泥について、以
下に示す試験を実施した。使用した引抜き汚泥の性状は
第1表に示すとおりである。
Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. In Examples and Comparative Examples, the analysis of hydrogen sulfide was performed using a gas detector tube [Gastec 4M,
4L or 4LL], and analysis of methyl mercaptan was performed using a gas detector tube [Gastec 71H or 71]. The lower detection limit concentration is 1 ppm for both hydrogen sulfide and methyl mercaptan. Examples 1 to 3 and Comparative Examples 1 to 3 The following tests were carried out on sludge from the initial settling basin containing excess sludge. The properties of the drawn sludge used are as shown in Table 1.

【0009】[0009]

【表1】 [Table 1]

【0010】(1)2リットルメスシリンダー沈降試験 試験汚泥について、無処理のまま、又は各種量の亜硝酸
イオンを添加し、2リットルメスシリンダー中での25
℃沈降試験を行い、沈降時間と沈降界面との関係を調べ
た。その結果を第2表−1及び図3に示す。
(1) Settling test of 2 liter graduated cylinder With respect to the test sludge, no treatment or addition of various amounts of nitrite ions was carried out.
A sedimentation test at ℃ was conducted to examine the relationship between sedimentation time and sedimentation interface. The results are shown in Table 2 and FIG.

【0011】[0011]

【表2】 [Table 2]

【0012】(注)表中、*印は汚泥の浮上又は汚泥層
に水の層が認められる。 (2)上澄み液及び沈降汚泥の臭気測定試験 上記(1)の沈降試験において、10時間経過後の上澄
み液、及び20時間経過後の汚泥を元の濃度の1.5倍
に濃縮した汚泥の臭気測定試験を行った。なお、20時
間経過後の浮上汚泥については、下澄み水を除去し濃縮
を行った。結果を第2表−2に示す。表における硫化水
素、メチルメルカプタンガスの濃度は、試料50mLを空
隙容積が530mLとなる容器にとり、2分間振とうした
後の気相に存在する各ガス濃度である。
(Note) In the table, the mark * indicates that the sludge is floating or that a water layer is observed in the sludge layer. (2) Odor measurement test of supernatant liquid and settled sludge In the settling test of the above (1), the supernatant liquid after elapse of 10 hours and the sludge after elapse of 20 hours were concentrated to 1.5 times the original concentration. An odor measurement test was performed. The floating sludge after elapse of 20 hours was concentrated by removing the supernatant water. Table 2 shows the results. The concentrations of hydrogen sulfide and methyl mercaptan gas in the table are the concentrations of each gas present in the gas phase after 50 mL of a sample is placed in a container having a void volume of 530 mL and shaken for 2 minutes.

【0013】[0013]

【表3】 [Table 3]

【0014】(3)濃縮汚泥保管後の臭気測定試験、汚
泥性状分析及び脱水試験 上記(1)の沈降試験において、20時間経過後の汚泥
を元の濃度の1.5倍に濃縮し、この汚泥をさらに25
℃で5時間又は10時間保管後、臭気測定試験を行うと
共に、10時間保管後の汚泥分析と下記の方法に従って
脱水試験を行った。なお、比較例1−2、実施例1−
2、実施例2−2及び実施例3−2は、1.5倍に濃縮
した汚泥にさらに第2表−3及び第2表−4に示す量の
亜硝酸イオンを添加した例である。該表中のNO2 -の合
計添加量は、1.5倍濃縮前の汚泥に換算した値であ
る。 <脱水試験>汚泥100mLを200mLビーカーに採取
し、市販のカチオン系高分子凝集剤[栗田工業(株)製、
登録商標名「クリフィックスCP604」]を150mg
/L添加し、凝集撹拌したのち、1分間重力ろ過し、ろ
過物を0.10MPaの圧搾圧力で1分間脱水処理して
脱水ケーキを得た。このようにして脱水試験により得ら
れたケーキの含水率を測定すると共に、ケーキ固形分1
t当たりのケーキ発生重量(t)及び無処理のケーキ発
生重量に対するケーキ減量率を算出した。これらの結果
を第2表−3及び第2表−4に示す。
(3) Odor measurement test, sludge property analysis and dehydration test after storage of concentrated sludge In the sedimentation test of the above (1), the sludge after 20 hours has been concentrated to 1.5 times the original concentration. 25 more sludges
After storage at 5 ° C. for 5 hours or 10 hours, an odor measurement test was performed, and a sludge analysis after storage for 10 hours and a dehydration test were performed according to the following method. In addition, Comparative Example 1-2 and Example 1-
2. Examples 2-2 and 3-2 are examples in which the amount of nitrite ions shown in Tables 2 and 3 is further added to the sludge 1.5 times concentrated. NO 2 in said surface - the total amount of a value converted to a 1.5-fold concentration prior to the sludge. <Dehydration test> 100 mL of sludge was collected in a 200 mL beaker, and a commercially available cationic polymer flocculant [Kurita Industry Co., Ltd.
Registered trademark name "Crifix CP604"] 150mg
/ L was added, and the mixture was subjected to coagulation and stirring, followed by gravity filtration for 1 minute, and the filtrate was subjected to a dehydration treatment at a compression pressure of 0.10 MPa for 1 minute to obtain a dehydrated cake. The moisture content of the cake obtained by the dehydration test in this way was measured, and the cake solid content was 1%.
The cake generation weight per t (t) and the cake loss rate relative to the untreated cake generation weight were calculated. The results are shown in Tables 2 and 3.

【0015】[0015]

【表4】 [Table 4]

【0016】[0016]

【表5】 [Table 5]

【0017】実施例4〜7及び比較例4 余剰汚泥を含まない最初沈澱池引抜き汚泥を最初沈澱処
理水を用いて所定の割合で希釈したものについて、以下
に示す試験を実施した。使用した引抜き汚泥の性状は第
3表に示すとおりである。
Examples 4 to 7 and Comparative Example 4 The following test was carried out on sludge from the first settling basin without excess sludge, which was first diluted at a predetermined ratio using settling water. The properties of the drawn sludge used are as shown in Table 3.

【0018】[0018]

【表6】 [Table 6]

【0019】(注)試験汚泥は、最初沈澱池引抜き汚泥
3容量部と最初沈澱処理水2容量部との混合物である。 (1)2リットルメスシリンダー沈降試験 試験汚泥について、無処理のまま、又は各種量の亜硝酸
イオンを添加し、2リットルメスシリンダー中での25
℃沈降試験を行い、沈降時間と沈降界面との関係を調べ
た。その結果を第4表−1及び図4に示す。
(Note) The test sludge is a mixture of 3 parts by volume of sludge withdrawn from the first settling basin and 2 parts by volume of first settling water. (1) Settling test of 2 liter graduated cylinder For test sludge, leave untreated or add various amounts of nitrite ions,
A sedimentation test at ℃ was conducted to examine the relationship between sedimentation time and sedimentation interface. The results are shown in Table 4-1 and FIG.

【0020】[0020]

【表7】 [Table 7]

【0021】(注)表中、*印は汚泥の浮上又は汚泥層
に水の層が認められる。 (2)上澄み液及び沈降汚泥の臭気測定試験 上記(1)の沈降試験において、10時間経過後の上澄
み液、及び20時間経過後の汚泥を元の濃度の1.8倍
に濃縮した汚泥の臭気測定試験を行った。なお、20時
間経過後の浮上汚泥については、下澄み水を除去し濃縮
を行った。結果を第4表−2に示す。
(Note) In the table, the * mark indicates the floating of sludge or the presence of a water layer in the sludge layer. (2) Odor measurement test of supernatant liquid and settled sludge In the settling test of the above (1), the sludge obtained by concentrating the supernatant liquid after elapse of 10 hours and the sludge after elapse of 20 hours to 1.8 times the original concentration. An odor measurement test was performed. The floating sludge after elapse of 20 hours was concentrated by removing the supernatant water. The results are shown in Table 4-2.

【0022】[0022]

【表8】 [Table 8]

【0023】(3)濃縮生汚泥と余剰濃縮汚泥との混合
汚泥保管後の臭気測定試験、汚泥性状分析及び脱水試験 第3表に示す汚泥性状を有する最初沈澱池引抜き汚泥を
最初沈澱処理水で5/3倍に希釈し、さらに1.8倍濃
縮した場合の計算値の汚泥濃度(SS21700mg/
L)と同濃度になるように、余剰濃縮汚泥(pH6.4
6、TS31200mg/L、VTS86.8%/TS、
SS30400mg/L、VSS87.2%/SS、繊維
分1.2%/SS)を最終沈澱処理水で希釈し、余剰調
整汚泥(pH6.54、TS22400mg/L、VTS8
6.2%/TS、SS21800mg/L、VSS87.3
%/SS、繊維分1.1%/SS)を得た。次に、上記
(1)の沈降試験において、20時間経過後の汚泥を元
の濃度の1.8倍に濃縮した汚泥3容量部と上記余剰調
整汚泥2容量部を混合し、試験汚泥を得た。この試験汚
泥を25℃で5時間又は10時間保管後、臭気測定試験
を行うと共に、10時間保管後の汚泥性状分析と前述の
方法に従って脱水試験を行った。なお、比較例4−2、
実施例4−2、実施例5−2及び実施例6−2は、該試
験汚泥に、さらに第4表−3及び第4表−4に示す量の
亜硝酸イオンを添加した例である。該表中のNO2 -の合
計添加量は、混合した余剰調整汚泥部分を除く、余剰汚
泥を含まない元の汚泥(1.8倍濃縮前の汚泥)に換算
した値である。これらの結果を第4表−3及び第4表−
4に示す。
(3) Odor measurement test, sludge property analysis and dewatering test after storage of mixed sludge of concentrated raw sludge and surplus concentrated sludge First-stage sedimentation tank with sludge properties shown in Table 3 The sludge concentration (SS21700mg / SS21) calculated by diluting 5/3 times and further condensing 1.8 times
L) to obtain the same concentration as the excess concentrated sludge (pH 6.4).
6, TS31200mg / L, VTS86.8% / TS,
SS 30400 mg / L, VSS 87.2% / SS, fiber content 1.2% / SS) were diluted with the final settling water, and the excess adjusted sludge (pH 6.54, TS22400 mg / L, VTS8)
6.2% / TS, SS21800mg / L, VSS87.3
% / SS, fiber content 1.1% / SS). Next, in the sedimentation test of the above (1), 3 volumes of sludge obtained by concentrating the sludge after 20 hours to 1.8 times the original concentration and 2 volumes of the surplus adjusted sludge were mixed to obtain test sludge. Was. After storing the test sludge at 25 ° C. for 5 hours or 10 hours, an odor measurement test was performed, and a sludge property analysis after storage for 10 hours and a dehydration test were performed according to the method described above. Note that Comparative Example 4-2,
Example 4-2, Example 5-2, and Example 6-2 are examples in which nitrite ions in the amounts shown in Table 4-3 and Table 4-4 were further added to the test sludge. NO 2 in said surface - the total amount of, excluding excess adjustment sludge portion mixed, a value obtained by converting the former without the excess sludge sludge (1.8 fold concentrate before sludge). These results are shown in Table 4-3 and Table 4
It is shown in FIG.

【0024】[0024]

【表9】 [Table 9]

【0025】[0025]

【表10】 [Table 10]

【0026】実施例8〜11 余剰汚泥を含まない最初沈澱池引抜き汚泥を最初沈澱処
理水を用いて、所定の希釈倍率になるように希釈し、濃
度の異なる汚泥を得た。この汚泥に所定量の亜硝酸イオ
ンを添加し、2リットルメスシリンダー中での25℃沈
降試験を行い、沈降時間と沈降界面との関係を調べた。
その結果を第6表及び図5に示す。使用した余剰汚泥を
含まない最初沈澱池引抜き汚泥の性状は、第5表に示す
とおりである。
Examples 8 to 11 Sludge drawn from the first settling basin without excess sludge was first diluted with a settling water to a predetermined dilution ratio to obtain sludges having different concentrations. A predetermined amount of nitrite ion was added to the sludge, and a sedimentation test at 25 ° C. was performed in a 2-liter measuring cylinder to examine the relationship between the sedimentation time and the sedimentation interface.
The results are shown in Table 6 and FIG. The properties of the first settling basin sludge that does not contain the used excess sludge are as shown in Table 5.

【0027】[0027]

【表11】 [Table 11]

【0028】[0028]

【表12】 [Table 12]

【0029】(注)NO2 -添加量1%補正:汚泥濃度1
0000mg/Lを基準とした場合の添加量換算値であ
る。 最大計算濃度:[汚泥濃度/最小沈降界面(%)]×1
00 *:汚泥の浮上又は汚泥層に水の層が認められる。 実施例12〜14及び比較例5〜7 余剰汚泥を含有する最初沈澱池引抜き汚泥について、以
下に示す試験を実施した。使用した引抜き汚泥の性状は
第7表に示すとおりである。
[0029] (Note) NO 2 - amount of 1% Correction: Sludge Concentration 1
This is a conversion value of the addition amount based on 0000 mg / L. Maximum calculated concentration: [sludge concentration / minimum settling interface (%)] x 1
00 *: Floating sludge or a water layer is observed in the sludge layer. Examples 12 to 14 and Comparative Examples 5 to 7 The following test was carried out on sludge from the initial settling basin containing excess sludge. The properties of the drawn sludge used are as shown in Table 7.

【0030】[0030]

【表13】 [Table 13]

【0031】(1)2リットルメスシリンダー沈降試験 余剰汚泥を含有する最初沈澱池引抜き汚泥をそのまま、
又は酸性物質を所定量添加し、このものに亜硝酸イオン
を添加せずに又は30mg/L添加して2リットルメスシ
リンダー中での25℃沈降試験を行い、沈降時間と沈降
界面との関係を調べた。その結果を第8表−1及び図6
に示す。
(1) 2 liter graduated cylinder settling test First settling basin sludge containing excess sludge was used as it was.
Alternatively, a predetermined amount of an acidic substance is added, and without adding nitrite ion or 30 mg / L, a sedimentation test is performed in a 2-liter measuring cylinder at 25 ° C., and the relation between the sedimentation time and the sedimentation interface is determined. Examined. The results are shown in Table 8-1 and FIG.
Shown in

【0032】[0032]

【表14】 [Table 14]

【0033】(注) PFS:ポリ硫酸第二鉄(Fe11%含有液状品) FC:塩化第二鉄(Fe13%含有液状品) *:汚泥の浮上又は汚泥層に水の層が認められる。 (2)上澄み液及び沈降汚泥の臭気測定試験 上記(1)の沈降試験において、10時間経過後の上澄
み液、及び20時間経過後の汚泥を元の濃度の1.5倍
に濃縮した汚泥の臭気測定試験を行った。なお、20時
間経過後の浮上汚泥については、下澄み水を除去し濃縮
を行った。結果を第8表−2に示す。
(Note) PFS: Ferric polysulfate (Liquid containing 11% Fe) FC: Ferric chloride (Liquid containing 13% Fe) *: Floating sludge or water layer in sludge layer. (2) Odor measurement test of supernatant liquid and settled sludge In the settling test of the above (1), the supernatant liquid after elapse of 10 hours and the sludge after elapse of 20 hours were concentrated to 1.5 times the original concentration. An odor measurement test was performed. The floating sludge after elapse of 20 hours was concentrated by removing the supernatant water. The results are shown in Table 8-2.

【0034】[0034]

【表15】 [Table 15]

【0035】[0035]

【発明の効果】本発明の汚泥処理方法は、余剰汚泥を含
有する最初沈澱池引抜き汚泥及び余剰汚泥を含有しない
最初沈澱池引抜き汚泥を、亜硝酸塩の存在下で重力濃縮
して、濃縮工程での汚泥浮上と臭気発生を防止すると共
に、以降の工程の臭気発生を抑制し、かつ最終工程の汚
泥の脱水性を向上させることができる。
According to the sludge treatment method of the present invention, the first settling tank drawn sludge containing surplus sludge and the first settling tank drawn sludge not containing surplus sludge are gravity-concentrated in the presence of nitrite, and are subjected to gravity concentration. In addition to preventing the floating of sludge and the generation of odor, the generation of odor in the subsequent steps can be suppressed, and the dewatering property of the sludge in the final step can be improved.

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

【図1】図1は、本発明における余剰汚泥を含有する最
初沈澱池引抜き汚泥の処理方法の1例を示す工程系統図
である。
FIG. 1 is a process flow chart showing one example of a method for treating sludge drawn from a first sedimentation basin containing excess sludge in the present invention.

【図2】図2は、本発明における余剰汚泥を含有しない
最初沈澱池引抜き汚泥の処理方法の1例を示す工程系統
図である。
FIG. 2 is a process flow chart showing one example of a method for treating sludge from a first sedimentation basin without excess sludge according to the present invention.

【図3】図3は、実施例1〜3及び比較例1〜3におい
て、沈降試験における沈降時間と沈降界面との関係を示
すグラフである。
FIG. 3 is a graph showing a relationship between a settling time and a settling interface in a settling test in Examples 1 to 3 and Comparative Examples 1 to 3.

【図4】図4は、実施例4〜7及び比較例4において、
沈降試験における沈降時間と沈降界面との関係を示すグ
ラフである。
FIG. 4 shows the results obtained in Examples 4 to 7 and Comparative Example 4.
It is a graph which shows the relationship between the sedimentation time and the sedimentation interface in a sedimentation test.

【図5】図5は、実施例8〜11において、沈降試験に
おける沈降時間と沈降界面との関係を示すグラフであ
る。
FIG. 5 is a graph showing a relationship between a settling time and a settling interface in a settling test in Examples 8 to 11.

【図6】図6は、実施例12〜14及び比較例5〜7に
おいて、沈降試験における沈降時間と沈降界面との関係
を示すグラフである。
FIG. 6 is a graph showing a relationship between a settling time and a settling interface in a settling test in Examples 12 to 14 and Comparative Examples 5 to 7.

【符号の説明】[Explanation of symbols]

1 最初沈澱池 2 活性汚泥槽 3 最終沈澱池 4 重力濃縮槽 5 汚泥貯留槽 6 脱水機 7 遠心濃縮機 A、B、C 亜硝酸塩 DESCRIPTION OF SYMBOLS 1 First settling tank 2 Activated sludge tank 3 Final settling tank 4 Gravity thickening tank 5 Sludge storage tank 6 Dehydrator 7 Centrifugal thickener A, B, C Nitrite

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4D059 AA04 AA05 BD19 BE08 BE16 BE26 BE31 BE38 BE53 BE57 BF12 BK01 CA28 CA29 DA23 DA24 DA32 DA33 DA70 DB11 EB05 EB11  ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4D059 AA04 AA05 BD19 BE08 BE16 BE26 BE31 BE38 BE53 BE57 BF12 BK01 CA28 CA29 DA23 DA24 DA32 DA33 DA70 DB11 EB05 EB11

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】余剰汚泥を含有する最初沈澱池引抜き汚泥
の処理方法であって、該引抜き汚泥に亜硝酸塩を、亜硝
酸イオンが10〜50mg/L対汚泥容量となるように添
加し、pH6未満にて該汚泥を重力濃縮することを特徴と
する汚泥処理方法。
1. A method for treating sludge from a primary sedimentation basin containing excess sludge, wherein nitrite is added to the sludge so as to have a nitrite ion content of 10 to 50 mg / L with respect to the sludge volume. A sludge treatment method, wherein the sludge is concentrated by gravity.
【請求項2】余剰汚泥を含有しない最初沈澱池引抜き汚
泥の処理方法であって、該引抜き汚泥に亜硝酸塩を添加
し、該汚泥を重力濃縮することを特徴とする汚泥処理方
法。
2. A method for treating sludge drawn from an initial sedimentation basin that does not contain excess sludge, wherein nitrite is added to the drawn sludge and the sludge is gravity-concentrated.
【請求項3】亜硝酸塩を、亜硝酸イオンが10〜70mg
/L対汚泥容量となるように添加する請求項2記載の汚
泥処理方法。
3. A nitrite comprising 10 to 70 mg of nitrite ions.
3. The method for treating sludge according to claim 2, wherein the sludge is added so as to be / L to sludge capacity.
【請求項4】引抜き汚泥を希釈する請求項1、2又は3
記載の汚泥処理方法。
4. The method of claim 1 wherein the sludge is diluted.
The sludge treatment method described in the above.
【請求項5】引抜き汚泥に酸性物質を添加する請求項1
ないし4のいずれかに記載の汚泥処理方法。
5. The method according to claim 1, wherein an acidic substance is added to the drawn sludge.
A sludge treatment method according to any one of claims 1 to 4.
【請求項6】重力濃縮後の汚泥を貯留する汚泥貯留槽に
亜硝酸塩を添加する請求項1ないし5のいずれかに記載
の汚泥処理方法。
6. The sludge treatment method according to claim 1, wherein nitrite is added to a sludge storage tank for storing sludge after gravity concentration.
JP2001175532A 2001-06-11 2001-06-11 Sludge treatment method Expired - Fee Related JP3900511B2 (en)

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FR2849020A1 (en) * 2002-12-23 2004-06-25 Otv Sa Treatment procedure for fermentable sludge or effluent consists of reducing pH level, adding nitrite salt, agitating, filtering and neutralizing
JP2013166108A (en) * 2012-02-15 2013-08-29 Kurita Water Ind Ltd Deodorizing method and deodorant kit
WO2014103549A1 (en) * 2012-12-28 2014-07-03 無臭元工業株式会社 Method for treating sewage
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KR20160024993A (en) 2013-08-22 2016-03-07 미츠비시 쥬코 칸쿄 카가쿠 엔지니어링 가부시키가이샤 Waste water treatment facility
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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004058651A3 (en) * 2002-12-23 2004-08-19 Otv Sa Fermentable effluent- and/or sludge-purification method and installation for implementing one such method
FR2849020A1 (en) * 2002-12-23 2004-06-25 Otv Sa Treatment procedure for fermentable sludge or effluent consists of reducing pH level, adding nitrite salt, agitating, filtering and neutralizing
JP2013166108A (en) * 2012-02-15 2013-08-29 Kurita Water Ind Ltd Deodorizing method and deodorant kit
WO2014103549A1 (en) * 2012-12-28 2014-07-03 無臭元工業株式会社 Method for treating sewage
JP2014128753A (en) * 2012-12-28 2014-07-10 Mushugen Industries Co Ltd Method for processing wastewater
KR20160024993A (en) 2013-08-22 2016-03-07 미츠비시 쥬코 칸쿄 카가쿠 엔지니어링 가부시키가이샤 Waste water treatment facility
JP2015112512A (en) * 2013-12-10 2015-06-22 無臭元工業株式会社 Wastewater treatment method
JP2016022421A (en) * 2014-07-18 2016-02-08 栗田工業株式会社 Sludge treatment method
JP2016055229A (en) * 2014-09-08 2016-04-21 栗田工業株式会社 Sludge concentration method
JP2016097373A (en) * 2014-11-25 2016-05-30 株式会社石垣 Sludge dehydration treatment method and sludge dehydration treatment system
JP2019005676A (en) * 2017-06-20 2019-01-17 栗田工業株式会社 Management method of sludge treatment
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JP2019005712A (en) * 2017-06-26 2019-01-17 栗田工業株式会社 Deodorant chemical injection control method and chemical injection control device for sludge

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