JPH0420676B2 - - Google Patents
Info
- Publication number
- JPH0420676B2 JPH0420676B2 JP58234794A JP23479483A JPH0420676B2 JP H0420676 B2 JPH0420676 B2 JP H0420676B2 JP 58234794 A JP58234794 A JP 58234794A JP 23479483 A JP23479483 A JP 23479483A JP H0420676 B2 JPH0420676 B2 JP H0420676B2
- Authority
- JP
- Japan
- Prior art keywords
- sludge
- tank
- treatment
- phosphorus
- passed
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000010802 sludge Substances 0.000 claims description 132
- 238000011282 treatment Methods 0.000 claims description 68
- 238000000034 method Methods 0.000 claims description 55
- 229910052698 phosphorus Inorganic materials 0.000 claims description 37
- 239000011574 phosphorus Substances 0.000 claims description 37
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 36
- 239000007788 liquid Substances 0.000 claims description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
- 230000008569 process Effects 0.000 claims description 18
- 229920000642 polymer Polymers 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 15
- 238000004062 sedimentation Methods 0.000 claims description 14
- 208000005156 Dehydration Diseases 0.000 claims description 13
- 230000018044 dehydration Effects 0.000 claims description 13
- 238000006297 dehydration reaction Methods 0.000 claims description 13
- 239000010865 sewage Substances 0.000 claims description 11
- 239000002562 thickening agent Substances 0.000 claims description 11
- 238000005496 tempering Methods 0.000 claims description 10
- 230000008719 thickening Effects 0.000 claims description 6
- 238000011221 initial treatment Methods 0.000 claims description 5
- 238000003860 storage Methods 0.000 description 11
- 230000000694 effects Effects 0.000 description 9
- 125000002091 cationic group Chemical group 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 4
- -1 alkali Metal salts Chemical class 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229920000620 organic polymer Polymers 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- 238000005273 aeration Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000008394 flocculating agent Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000005086 pumping Methods 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000004065 wastewater treatment Methods 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 150000003926 acrylamides Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- 235000012255 calcium oxide Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 230000001373 regressive effect Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- VMSBGXAJJLPWKV-UHFFFAOYSA-N 2-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=C VMSBGXAJJLPWKV-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 229920006319 cationized starch Polymers 0.000 description 1
- 238000009264 composting Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000012851 eutrophication Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Treatment Of Sludge (AREA)
Description
(発明の利用分野)
本発明は、下水、産業廃水などのリンを含有す
る有機性廃水(以下汚水という)を対象として、
嫌気−好気式活性汚泥により汚水中のリンを除去
する汚水処理法において、発生する余剰汚泥を処
理する方法に関する。
(発明の背景)
一般に、活性汚泥を利用した生物学的汚水処理
法は、汚水(原水)を、最初沈澱池(以下初沈と
略称する)に通して固形分、BODの一部を沈降
除去し、次いで二次処理工程に送給してBODを
分解させ、この曝気槽出口混合液を最終沈澱池
(以下終沈と略称する)に送給して汚泥を沈降分
離させ、分離後の上澄液は処理水として排水系に
送り、他方沈降分離された汚泥は、その一部を前
記曝気槽のBOD分解に必要な返送汚泥として曝
気槽入口側に返送し、またその余の汚泥は余剰汚
泥として終沈より引き抜いて脱水固形化の処理工
程に送るようにした方法としてよく知られてい
る。特に、この方法は、前記二次処理の工程中
で、初沈より流入する一次処理水と返送汚泥を、
嫌気槽−好気槽ん緒順に通すようにした場合に
は、汚水中のBOD除去と同時に脱リンも行なえ
る方法(なお、前記嫌気槽と好気槽の間に脱窒素
槽を設けて、前記好気槽からの循環水を与える場
合には、脱リンに加え脱窒素をも行なえる方法と
なるが、以下の説明では、これらの両者を含めて
脱リン能力を有する生物処理法をA/O法と総称
する)となるため、二次処理工程の段階で、薬品
を使用することなく、処理水排出水域の富栄養化
源の一つとなるリンを除去できる処理法として近
時注目されてきている。
ところで前記A/O法でいうリン除去とは、液
中のリンを汚泥に蓄積させることをいい、その後
この混合液を嫌気条件下に置くと、汚泥はリンを
再び液中に放出してしまう性質がある。このた
め、終沈から引き抜いた余剰汚泥の処理を嫌気の
条件下で行なう場合には、該余剰汚泥中のリンの
多くは液中に放出され、余剰汚泥の処理に伴つて
生ずる脱離水を介して前記汚水処理系に戻り、結
局リンが回帰する悪循環を招いてしまうことにな
る。
これらのことから、前記A/O法による汚水処
理系については回帰リンを防止、低減させる必要
が望まれ、例えば特開昭56−150487号公報、特開
昭56−150500号公報等の提案がされているが、い
ずれも実用性、特に運転コストならびに汚泥処理
処分等の面で難点がある。
そこで本発明者等は、A/O法に従つた二次処理
工程の好気槽から排出される、一般に溶存酸素の
高い混合液を、そこに含まれる汚泥を余剰汚泥と
して処理すべき相当分だけ、直接、遠心型又は
過型の機械濃縮機に送給し、ここで、溶存酸素の
経時的低下による嫌気条件の現出前に迅速濃縮を
行ない、更に脱水処理工程に送るようにした新規
な余剰汚泥処理方法を提案した。
かかる方法によれば、1時間以内程度の迅速濃
縮にて汚泥から液中に放出するリン濃度を0.4〜
0.8mg/に抑えることができ、従来の終沈より
余剰汚泥を引き抜く方式の場合にリン濃度が通常
20〜30mg/程度となつていることに比べて、回
帰リンの低減に極めて有効なものとなる効果があ
り、また脱水工程に送給する汚泥の濃縮程度も従
来法の場合に比べて数倍程度とできるため、脱水
の前処理として添加する凝集剤の量も大幅に低減
されるなどの様々な効果が得られた。
ところで、前記の改良とは別に、近年、脱水工
程の処理方法についても種々の改善がなされてき
ており、特に脱水機の前段において行なう凝集剤
添加による汚泥の調質処理については、高分子凝
集剤のめざましい発展があつて、これが使用され
る機会が多くなつてきており、またこれに伴つ
て、使用される脱水機の型も真空脱水機からベル
トプレス脱水機、遠心脱水機等に変つてきている
現状がある。
しかし、このような高分子凝集剤を用いる処理
は、前記の本発明者等の開発した、機械濃縮機に
よるA/O法の好気槽出口混合液の迅速濃縮方式
に基づく余剰汚泥処理法との有機的な関連性にお
いて改良発展されてきたものでないために、前記
各段階の処理、すなわち機械濃縮機を用いた迅速
濃縮と、高分子凝集剤を用いた脱水処理を組合せ
て行なう場合には、これら両者の処理の優れた効
果をそれぞれ発揮させる上で、更に改善すべきい
くつかの問題のあることが認められる。
例えば、前記高分子凝集剤は、汚泥から液中に
リンが放出される場合に、その固定(不溶化)に
格別の効果を示すものではないから、脱離水を介
してのリン回帰を充分低減させるためには、脱水
処理を迅速に行い、あるいはリン固定の別途の工
夫が望まれる。他方、前記機械濃縮機による迅速
濃縮で得られた濃縮汚泥は、高分子凝集剤等を加
えて調質処理しなければそのままでは脱水不可能
である。
(発明の目的)
本発明は、これらの種々の点に鑑み、A/O法
における余剰汚泥を好気槽出口混合液の迅速濃縮
により濃縮汚泥として得た後、これを高分子凝集
剤で調質して脱水処理するようにした汚泥処理法
において、これら一連の工程の効果をそれぞれ有
効に発揮させることができるようにした新規なる
汚泥処理法を提供せんとするものである。
また本発明の別の目的は、前記した目的を達成
した上で、機械濃縮の処理と脱水処理の2つを、
時間的に連続することなく行なうことを可能と
し、これにより脱水処理設備の稼働を夜間あるい
は休日において停止できるようにすることにあ
る。
(発明の概要)
前記した目的を達成するための本願発明の基本
的要旨とするところは、A/O法の好気槽出口混
合液を濃縮した濃縮汚泥Aに対し、繊維分の多い
初沈からの初沈汚泥Bを合流させ、これにより脱
水処理時における過速度の増大、ケーキ含水率
の低下を図るようにしたのであり、具体的には本
願の第1番目の発明の要旨は、初沈による一次処
理の次段に、被処理水を嫌気槽−好気槽の順に通
してリンを汚泥中に蓄積させる二次処理の工程を
もつ汚水処理法において、前記好気槽出口混合液
の一部を、直接、遠心型又は過型機械濃縮機で
迅速濃縮した濃縮汚泥(以下汚泥Aという)と、
前記最初沈澱池からの初沈汚泥(以下汚泥Bとい
う)とを、合流させた後速やかに脱水処理の工程
に送給させると共に、機械濃縮後の脱水前処理と
して高分子凝集剤により調質処理することを特徴
とする汚泥の処理方法にある。
また本願第2番目の発明は、前記方法における
効果を担保しつつ、実際の汚水処理施設において
みられる設備の稼動状況、すなわち特に脱水処理
設備の夜間、休日での停止を実現するために、前
記第1番目発明における機械濃縮後の濃縮汚泥A
を、汚泥から溶出するリンの固定に有効なCa塩
の添加を条件として、貯溜槽に溜めておく(ただ
し汚泥の調質処理は貯溜後に行なう)ことを可能
とした点に特徴がある。
なお、Ca塩添加を条件とした汚泥Aの貯溜は、
汚泥Bとの合流時であつてもよいし、汚泥Bとの
合流前において行なつてもよく、特に後者の場合
は汚泥Aと汚泥Bを脱水処理の直前において合流
させるという好ましい態様が実現できる利点があ
る。
本発明において、機械濃縮機による迅速濃縮の
程度は一般に出来るだけ高濃度となるようにする
ことが望ましいが、濃縮機に送給される混合液の
流量、濃縮機の容量、能力、嫌気性条件となるこ
との悪影響防止のために滞溜時間を出来るだけ短
かくすること(通常装置内滞溜時間を1時間以内
とすることが望ましい)、等々の関係において設
定され、汚泥濃度が好ましくは3〜8重量%、最
適には4〜6重量%程度とすることがよい。
本発明において、好気槽出口混合液の2方向へ
の送給量配分制御は、例えば、好気槽から終沈へ
の流出渠より、ポンプによつて機械濃縮機に汲み
上げる好気槽出口混合液の量を制御することで行
なえばよい。この場合、前記ポンプの汲み上げ量
制御は、好気槽からの二次処理水排出量、該処理
水中の汚泥濃度等によつて、終沈において沈降分
離して得られる汚泥量が変化することに関連、対
応し、返送汚泥分を終沈において常に確保する必
要から、例えば、終沈で沈降分離した汚泥の界面
レベルを所定の一定範囲内にあるように、前記各
送給量を制御してなされる。具体的には、例えば
終沈の汚泥界面レベル検出器を設置し、該検出器
と前記ポンプの駆動機構を連動させて行なうよう
にすればよい。
本発明において、機械濃縮機が遠心型および
過型のものに特定されているのは、処理水の装置
内滞溜時間を短かくして嫌気条件の現出を防ぎ、
高濃度の濃縮を達成し、更に設備的な大きさ、操
作性等々を考慮した上で、本発明の効果を充分発
揮させるためである。
機械濃縮機としては、例えば横型遠心濃縮機、
竪型遠心濃縮機、特開昭58−138596号公報に提案
された布筒濃縮機等を代表的に挙げることがで
きる。
脱水機としては、ベルトプレス脱水機、スクリ
ユープレス脱水機、遠心脱水機等の迅速な処理
(1時間程度以下の脱水処理)を行なうことがで
きるものが代表的に挙げられる。
本発明において、機械濃縮機により迅速濃縮さ
れた濃縮汚泥Aに対して合流される初沈汚泥B
は、最初沈澱池で沈降分離して得られたものを、
濃縮槽で更に沈降分離した汚泥を用いることがよ
い。この汚泥Bの濃縮程度は、濃縮槽の容量、滞
溜時間、原水の種類等々に応じて変化するが、一
般には高濃度とされることがよく、好ましくは固
形分として3〜8重量%、最適には4〜6重量%
程度とすることが望ましい。
本発明において使用される高分子凝集剤は、汚
泥Aと汚泥Bを別々に調質処理する場合において
も同種のものを用いることが望ましく、高分子凝
集剤としては、既知のカチオンポリマーあるいは
カチオンとアニオンのポリマーを併用して使用す
ることができる。具体的には、例えばカチオン性
有機高分子凝集剤としてはN,N′−ジメチルア
ミノアルキルアクリレートあるいはメタクリレー
トでアルキル基の炭素数が2あるいは3のものの
酸塩、ビニルベンジルモノジトリメチルアンモニ
ウムの酸塩、アクリルアミドのカチオン変性物の
酸塩、ビニルピリジンおよびその置換誘導体、ア
クリルアミンおよびその置換誘導体のようなカチ
オン性単量体の単一重合体および共重合体などが
使用できる。
また上記のようなカチオン性単量体とアクリル
アミド、アクリロニトリル、アクリル酸アルキル
エステルのような単量体との共重合物、さらにポ
リビニルイミダゾリンの酸塩、キトサンの酸塩、
澱粉のカチオン化物なども使用できる。
またカチオン性有機高分子凝集剤、アニオン性
有機高分子凝集剤を併用する場合には、上記カチ
オン性有機高分子凝集剤と共に、アニオン性有機
高分子凝集剤としてアクリル酸、メタクリル酸お
よびそれらのアルカリ金属塩、アクリルアミドの
スルホメチル化物およびそのアルカリ金属塩、ビ
ニルベンゼンスルフオン酸、スチレンスルホン酸
およびそのアルカリ金属塩、ビニルスルフオン酸
およびそのアルカリ金属塩、無水マレイン酸など
の単一重合体および共重合体などが使用される。
また上記のようなアニオン性単量体とアクリルア
ミド、アクリロニトリル、アクリル酸アルキルエ
ステルのように単量体との共重合物、さらにアル
ギン酸ソーダ、キチンのアニオン変性物なども使
用できる。
本願の第1番目の発明において、汚泥Aと汚泥
Bを合流させる場合に、高分子凝集剤の添加によ
る調質処理は、合流の前に各汚泥について行なつ
てもよいし、合流後に行なつてもよいが、合流に
よつて一般に汚泥Aの嫌気化は促進されることに
なるので、脱水処理時の脱離水中に含まれる回帰
リンを出来るだけ低減させるためには、調質処理
後で脱水処理装置に導く直前において汚泥A,B
を合流させることが望ましい。合流させた汚泥
A,Bは攪拌して部分的な汚泥の偏在をなくすこ
とが実用上望ましい。
本願第2番目の発明において、汚泥Aを貯溜す
るのは、一般的には機械濃縮機で迅速濃縮された
状態のまま貯溜槽で行なうことがよいが、貯溜槽
には初沈汚泥Bを合流させてもよい。
汚泥Aを貯溜する場合、この汚泥Aは初沈汚泥
Bとは異つてリンを蓄積したものであるから、貯
溜時間が長くなり溶存酸素(DO)の低下が進む
に従つて嫌気条件が現出すると、蓄積したリンを
液中に放出することになる。したがつてこのよう
な放出されたリンを固定することにより、脱水処
理時の脱離水を介して汚水処理系にリンが回帰す
ることを可及的小ならしめるため、Ca塩が添加
される。このCa塩の添加量は、汚泥Aの貯溜時
間、汚泥濃度、温度、二次処理水中のDOの量
等々との関係に応じて選択されるが、一般的には
汚泥Aの固形物比で5〜10重量%であることが好
ましい。Ca塩として具体的には、例えば消石灰
〔Ca(OH)2〕、生石灰〔CaO〕を挙げることがで
きる。
(発明の実施例)
実施例 1
第1図は本発明の一実施例の概要フローを示し
たものであり、原水の流入される初沈1で一次処
理を行ない、一次処理水を次段のA/O法に従つ
て構成された二次処理設備2に送給する。
二次処理設備2は、流入水をまず嫌気槽3に入
れ、次いで下流側の好気槽4に移送して、嫌気−
好気処理によりBODを生物分解処理すると共に、
リンを汚泥中に蓄積する形で液中から除去する。
この後、混合液は好気槽4の出口より流出渠5
を経て、主には終沈6に送給され、また混合液の
一部は流出渠5から図示しないポンプにより機械
濃縮機7に汲み上げ送給される。この機械濃縮機
7は遠心型(又は加圧過型)の濃縮機として構
成され、通常1時間程度以内、好ましくは30分程
度の滞溜時間で、二次処理水を好ましくは3〜8
重量%、最適には4〜6重量%の汚泥濃度まで濃
縮する。この濃縮処理においては処理が極めて迅
速であるため溶存酸素DOの低下が進行する前に
濃縮が進行し、脱離水として初沈1の入口に戻さ
れる液の中に含まれるリンは、処理水のリン濃度
と略同程度である。
濃縮後の汚泥Aはクツシヨンタンク8を経由し
て、ポンプ9により調質槽10に送給され、ポリ
マー添加による所定の調質がなされた後、後記す
る初沈汚泥Bと合流され、混合槽11で攪拌後直
ちにベルトプレス脱水機12に導かれる。脱水時
の脱離水S*は初沈入口に戻される。
一方、前記合流される初沈汚泥Bは、初沈1で
沈降分離された汚泥を濃縮槽13に送り、ここで
重力沈降により更に沈降分離した汚泥として得ら
れ、ポンプ14によりこれを前記とは別の調質槽
15に送給して、所定の調質処理後汚泥Aに合流
される。
前記において2つの調質槽10,15で使用さ
れるポリマー(高分子凝集剤)は凝集程度を揃え
る等のために同種のものを用いることがよい。
なお、終沈6に送給された混合液は、該終沈に
おいて所定の時間滞溜して汚泥を沈降分離させ、
上澄みは処理水として排水系に送られ、汚泥は返
送汚泥として嫌気槽の入口に送給される。そして
このような処理を行なう終沈6への二次処理水の
流入量は、例えば、図示しない、汚泥界面レベル
の検出手段を用いて、該レベルが一定範囲内にあ
るように前記機械濃縮機へのポンプ汲み上げ量を
制御することで行なうことでなされる。
以上のフローに示される汚水処理系において行
なつた汚泥処理の試験結果を、汚泥Aを汚泥Bと
合流させない場合のものと比較して下記表1に示
す。
(Field of Application of the Invention) The present invention targets organic wastewater containing phosphorus (hereinafter referred to as wastewater) such as sewage and industrial wastewater.
The present invention relates to a method for treating excess sludge generated in a sewage treatment method for removing phosphorus from sewage using anaerobic-aerobic activated sludge. (Background of the invention) In general, biological wastewater treatment methods using activated sludge pass wastewater (raw water) through an initial settling tank (hereinafter referred to as initial settling tank) to remove solids and a portion of BOD. The sludge is then sent to the secondary treatment process to decompose the BOD, and the mixed liquid at the outlet of the aeration tank is sent to the final settling tank (hereinafter referred to as final settling) to settle and separate the sludge. The clear liquid is sent to the drainage system as treated water, while a portion of the sedimented and separated sludge is returned to the aeration tank inlet as return sludge necessary for BOD decomposition in the aeration tank, and the remaining sludge is used as surplus sludge. This is a well-known method in which sludge is extracted from the final sedimentation stage and sent to a dehydration and solidification treatment process. In particular, in this method, during the secondary treatment process, the primary treatment water and return sludge flowing in from the initial settling are
If the water is passed in the order of anaerobic tank and aerobic tank, it is possible to remove BOD from the wastewater and also dephosphorize it at the same time (in addition, a denitrification tank is provided between the anaerobic tank and the aerobic tank, When circulating water from the aerobic tank is supplied, it is a method that can perform denitrification in addition to dephosphorization, but in the following explanation, A biological treatment method that has dephosphorization ability, including both of these, will be used. /O method), which has recently attracted attention as a treatment method that can remove phosphorus, which is one of the sources of eutrophication in treated water discharge areas, without using chemicals at the secondary treatment stage. It's coming. By the way, phosphorus removal in the A/O method refers to accumulating phosphorus in the liquid into sludge, and if this mixed liquid is then placed under anaerobic conditions, the sludge will release phosphorus back into the liquid. It has a nature. Therefore, when the surplus sludge extracted from final settling is treated under anaerobic conditions, most of the phosphorus in the surplus sludge is released into the liquid and is absorbed through the desorbed water generated during the treatment of the surplus sludge. The phosphorus then returns to the sewage treatment system, resulting in a vicious cycle in which the phosphorus returns. For these reasons, it is desirable to prevent and reduce regressive phosphorus in wastewater treatment systems using the A/O method, and proposals such as those in JP-A-56-150487 and JP-A-56-150500 have been proposed. However, all of them have drawbacks in terms of practicality, especially operating costs and sludge treatment and disposal. Therefore, the inventors of the present invention have investigated how to treat a mixed liquid with generally high dissolved oxygen, which is generally discharged from an aerobic tank in a secondary treatment process according to the A/O method, to the extent that the sludge contained therein should be treated as surplus sludge. The novel method is to directly feed the liquid to a centrifugal or permeable mechanical concentrator, where it is quickly concentrated before the occurrence of anaerobic conditions due to a decrease in dissolved oxygen over time, and then sent to a dehydration process. A method for treating surplus sludge was proposed. According to this method, the phosphorus concentration released from sludge into the liquid can be reduced to 0.4 to 0.4 with rapid concentration within about one hour.
The phosphorus concentration can be suppressed to 0.8mg/, which is lower than the normal phosphorus concentration when using the conventional method of drawing out excess sludge from final settling.
It is extremely effective in reducing regressive phosphorus, and the degree of concentration of sludge sent to the dewatering process is several times that of conventional methods. As a result, the amount of flocculant added as a pretreatment for dehydration was significantly reduced, and various effects were obtained. By the way, in addition to the above-mentioned improvements, various improvements have been made in recent years in the treatment method of the dewatering process.In particular, in the treatment of sludge by adding a flocculant in the front stage of the dehydrator, polymer flocculants have been used. There has been a remarkable development, and the opportunities for this to be used are increasing, and along with this, the types of dehydrators used have also changed from vacuum dehydrators to belt press dehydrators, centrifugal dehydrators, etc. There is a current situation. However, such treatment using a polymer flocculant is different from the surplus sludge treatment method based on the rapid concentration method of the aerobic tank outlet mixture using a mechanical thickener, developed by the present inventors. Since the organic relationship between the two has not been improved and developed, when the above-mentioned steps are combined, i.e., rapid concentration using a mechanical concentrator and dehydration using a polymer flocculant, It is recognized that there are some problems that need to be further improved in order to bring out the excellent effects of these two treatments. For example, the polymer flocculant does not show any particular effect on fixing (insolubilizing) phosphorus when it is released from sludge into the liquid, so it is sufficient to sufficiently reduce phosphorus return via desorbed water. In order to achieve this, it is desirable to perform dehydration treatment quickly or to devise a separate method for phosphorus fixation. On the other hand, the thickened sludge obtained by rapid concentration using the mechanical thickener cannot be dehydrated as it is unless a polymer flocculant or the like is added to the sludge for tempering treatment. (Object of the Invention) In view of these various points, the present invention has been developed by obtaining thick sludge by rapidly concentrating the mixed liquid at the outlet of an aerobic tank from surplus sludge in the A/O method, and then preparing this with a polymer flocculant. The present invention aims to provide a new sludge treatment method in which the effects of each of these series of steps can be effectively exhibited in a sludge treatment method in which sludge is hydrated and dehydrated. Another object of the present invention is to achieve the above-mentioned object and to perform two processes, mechanical concentration treatment and dehydration treatment.
The purpose is to make it possible to perform the dehydration treatment without continuous time, thereby making it possible to stop the operation of the dehydration treatment equipment at night or on holidays. (Summary of the Invention) The basic gist of the present invention for achieving the above-mentioned object is that the concentrated sludge A obtained by concentrating the mixed liquid at the outlet of the aerobic tank of the A/O method is subjected to initial sedimentation with a high fiber content. The first settled sludge B from the sludge B is combined with the first sludge B, thereby increasing the overspeed during dewatering treatment and reducing the moisture content of the cake. Specifically, the gist of the first invention of the present application is In a wastewater treatment method that has a secondary treatment step in which the water to be treated is passed through an anaerobic tank and an aerobic tank in order to accumulate phosphorus in the sludge after the primary treatment by sedimentation, the mixed liquid at the outlet of the aerobic tank is Thickened sludge (hereinafter referred to as sludge A), a portion of which was quickly concentrated directly using a centrifugal or permeable mechanical thickener;
After the initial settling sludge (hereinafter referred to as sludge B) from the initial settling tank is combined, it is immediately sent to the dewatering process, and is subjected to tempering treatment using a polymer flocculant as a pretreatment for dewatering after mechanical concentration. A sludge treatment method characterized by: In addition, the second invention of the present application provides the above-mentioned method in order to achieve the operating conditions of the equipment found in actual sewage treatment facilities, that is, in particular, to stop the dewatering treatment equipment at night and on holidays, while ensuring the effects of the method. Thickened sludge A after mechanical thickening in the first invention
The sludge is characterized by being able to be stored in a storage tank (however, the sludge is tempered after storage), provided that Ca salt, which is effective in fixing phosphorus eluted from the sludge, is added. In addition, the storage of sludge A with the addition of Ca salt is as follows:
It may be carried out at the time of merging with sludge B or before merging with sludge B. In the latter case in particular, a preferable embodiment of merging sludge A and sludge B immediately before dewatering treatment can be realized. There are advantages. In the present invention, it is generally desirable for the level of rapid concentration by the mechanical concentrator to be as high as possible, but the flow rate of the mixed liquid fed to the concentrator, the capacity and capacity of the concentrator, In order to prevent the negative effects of sludge concentration, the retention time should be kept as short as possible (normally, it is desirable to keep the retention time in the device within 1 hour), etc., and the sludge concentration is preferably 3. The content is preferably about 8% by weight, most preferably about 4% to 6% by weight. In the present invention, the feeding amount distribution control of the aerobic tank outlet mixed liquid in two directions is performed, for example, by pumping the aerobic tank outlet mixed liquid from the outflow conduit from the aerobic tank to the final sedimentation to the mechanical concentrator. This can be done by controlling the amount of liquid. In this case, the amount of pumping by the pump is controlled because the amount of sludge obtained by sedimentation and separation in the final sedimentation changes depending on the amount of secondary treated water discharged from the aerobic tank, the sludge concentration in the treated water, etc. Correspondingly, since it is necessary to always secure the amount of returned sludge in the final settling, for example, each of the above-mentioned feeding rates is controlled so that the interface level of the sludge separated by sedimentation in the final settling is within a predetermined range. It will be done. Specifically, for example, a sludge interface level detector for final settling may be installed, and the detector and the drive mechanism of the pump may be linked together. In the present invention, the mechanical concentrator is specified as a centrifugal type or a centrifugal type because it shortens the residence time of treated water in the device to prevent the appearance of anaerobic conditions.
This is to achieve high concentration concentration and to fully exhibit the effects of the present invention, taking into account equipment size, operability, etc. Examples of mechanical concentrators include horizontal centrifugal concentrators,
Typical examples include a vertical centrifugal concentrator and a cloth tube concentrator proposed in Japanese Unexamined Patent Publication No. 138596/1983. Typical examples of the dehydrator include those that can perform rapid treatment (dehydration treatment in about 1 hour or less), such as belt press dehydrators, screw press dehydrators, and centrifugal dehydrators. In the present invention, initial settling sludge B is combined with thickened sludge A rapidly thickened by a mechanical thickener.
is obtained by sedimentation and separation in a sedimentation tank,
It is preferable to use sludge that has been further sedimented and separated in a thickening tank. The degree of concentration of this sludge B varies depending on the capacity of the thickening tank, residence time, type of raw water, etc., but in general it is often set to a high concentration, preferably 3 to 8% by weight as a solid content. Optimally 4-6% by weight
It is desirable to keep it at a certain level. It is desirable to use the same kind of polymer flocculant used in the present invention even when sludge A and sludge B are subjected to separate tempering treatments.As the polymer flocculant, known cationic polymers or cationic Anionic polymers can be used in combination. Specifically, examples of cationic organic polymer flocculants include acid salts of N,N'-dimethylaminoalkyl acrylate or methacrylate with an alkyl group having 2 or 3 carbon atoms, and vinylbenzylmonoditrimethylammonium acid salts. Homopolymers and copolymers of cationic monomers such as , acid salts of cationically modified acrylamide, vinylpyridine and substituted derivatives thereof, acrylamine and substituted derivatives thereof, and the like can be used. In addition, copolymers of the above-mentioned cationic monomers and monomers such as acrylamide, acrylonitrile, and acrylic acid alkyl esters, as well as polyvinylimidazoline acid salts, chitosan acid salts,
Cationized starch can also be used. In addition, when using a cationic organic polymer flocculant and an anionic organic polymer flocculant together, in addition to the above cationic organic polymer flocculant, acrylic acid, methacrylic acid, and their alkali Metal salts, sulfomethylated acrylamide and its alkali metal salts, vinylbenzenesulfonic acid, styrenesulfonic acid and its alkali metal salts, vinylsulfonic acid and its alkali metal salts, maleic anhydride, and other homopolymers and copolymers etc. are used.
Further, copolymers of the above-mentioned anionic monomers with monomers such as acrylamide, acrylonitrile, and acrylic acid alkyl esters, as well as anion-modified products of sodium alginate and chitin, can also be used. In the first invention of the present application, when sludge A and sludge B are combined, the refining treatment by adding a polymer flocculant may be performed on each sludge before the combination, or it may be performed after the combination. However, since the anaerobization of sludge A is generally promoted by the merging, in order to reduce as much as possible the regressed phosphorus contained in the desorbed water during dewatering, it is necessary to Sludge A and B immediately before being led to the dewatering treatment equipment
It is desirable to merge the two. It is practically desirable to stir the combined sludges A and B to eliminate partial uneven distribution of the sludge. In the second invention of the present application, it is generally preferable to store the sludge A in a storage tank in a state that has been quickly concentrated using a mechanical thickener, but the sludge B is combined with the first settled sludge B in the storage tank. You may let them. When storing sludge A, sludge A is different from initially settled sludge B in that it has accumulated phosphorus, so as the storage time becomes longer and dissolved oxygen (DO) decreases, anaerobic conditions will appear. This causes the accumulated phosphorus to be released into the liquid. Therefore, by fixing such released phosphorus, Ca salt is added in order to minimize the return of phosphorus to the sewage treatment system via the water released during dehydration treatment. The amount of Ca salt added is selected depending on the relationship with the storage time of sludge A, sludge concentration, temperature, amount of DO in the secondary treatment water, etc., but it is generally determined by the solid content ratio of sludge A. It is preferably 5 to 10% by weight. Specific examples of the Ca salt include slaked lime [Ca(OH) 2 ] and quicklime [CaO]. (Embodiments of the Invention) Example 1 Figure 1 shows a general flow of an embodiment of the present invention, in which primary treatment is performed in the initial settling 1 where raw water is introduced, and the primary treated water is sent to the next stage. It is fed to a secondary treatment facility 2 configured according to the A/O method. The secondary treatment equipment 2 first puts inflow water into an anaerobic tank 3, then transfers it to an aerobic tank 4 on the downstream side, and
In addition to biodegrading BOD through aerobic treatment,
Phosphorus is removed from the liquid by accumulating it in the sludge. After this, the mixed liquid flows out from the outlet of the aerobic tank 4 into the conduit 5.
The mixed liquid is mainly sent to the final settling 6, and a part of the mixed liquid is pumped up from the outflow conduit 5 by a pump (not shown) and sent to the mechanical concentrator 7. This mechanical concentrator 7 is configured as a centrifugal type (or pressurized type) concentrator, and the residence time is usually within about 1 hour, preferably about 30 minutes, and the secondary treated water is preferably
Concentrate to a sludge concentration of 4-6% by weight, optimally 4-6% by weight. In this concentration process, the process is extremely rapid, so the concentration progresses before the dissolved oxygen DO decreases, and the phosphorus contained in the liquid returned to the inlet of initial precipitation 1 as desorbed water is removed from the treated water. It is approximately the same level as the phosphorus concentration. The concentrated sludge A is sent via the cushion tank 8 to the conditioning tank 10 by the pump 9, and after being subjected to a predetermined conditioning by adding polymer, it is combined with the initial settling sludge B, which will be described later, and mixed. Immediately after being stirred in tank 11, it is led to belt press dehydrator 12. The desorbed water S * during dehydration is returned to the initial settling port. On the other hand, the combined initial settling sludge B is obtained by sending the sludge that has been settled and separated in the initial settling 1 to the thickening tank 13, where it is further settled and separated by gravity settling, and is obtained as sludge that is separated by the pump 14. It is fed to another tempering tank 15 and merged with sludge A after a predetermined tempering treatment. In the above, the polymers (polymer flocculants) used in the two tempering tanks 10 and 15 are preferably of the same type in order to equalize the degree of aggregation. In addition, the mixed liquid sent to the final settling 6 is retained in the final settling for a predetermined period of time to settle and separate the sludge,
The supernatant is sent to the drainage system as treated water, and the sludge is sent to the inlet of the anaerobic tank as return sludge. The amount of secondary treated water flowing into the final sedimentation unit 6 that performs such treatment is determined using, for example, a sludge interface level detection means (not shown) in the mechanical thickener so that the level is within a certain range. This is done by controlling the amount of pumping into the tank. The test results of sludge treatment carried out in the sewage treatment system shown in the above flow are shown in Table 1 below, in comparison with the results when sludge A is not combined with sludge B.
【表】
前記表より明らかな如く、汚泥Aを単独に脱水
処理する場合に比べ、汚泥A,Bを合流させて処
理した場合には、脱水処理に要する時間、ケーキ
の含水率等の点で優れていることが認められた。
なお、前記第1図に示した実施例1では、機械
濃縮機から得た汚泥を途中貯溜することなく速や
かにベルトプレス機まで送給することで、嫌気状
態の現出に伴うリンの液中への放出を出来るだけ
防止するが望ましく、したがつて初沈汚泥Bの合
流も出来るだけ脱水処理の直前で行なうことがよ
いが、高分子凝集剤の添加による調質操作の簡便
化を図る上では、合流後の汚泥A,Bを一つの調
質槽で攪拌させるようにしてもよく、この場合に
も実用上支障のない範囲に回帰リンの量を抑えて
汚泥処理を行なうことができる。
実施例 2
第2図に示す本実施例2は、第1図に比べて機
械濃縮機7で迅速濃縮した濃縮汚泥Aを、貯溜槽
8′に貯溜すると共に所定量のCa塩を添加し、更
に初沈汚泥Bをこの貯溜槽8′に合流させた点に
特徴がある。したがつて調質槽10は、合流した
汚泥A,Bに対して一つのみとされている。
このような構成によれば、第1図に示した汚泥
処理の利点を担保して更に実用的に優れた汚泥処
理の設備を実現できることになる。
すなわち、貯溜槽8′において、長時間の汚泥
滞溜により嫌気状態が現出し、汚泥からリンが液
中に放出することがあつても、このリンは添加さ
れたCa塩により固定化され、脱水処理の際に脱
離水S*中にリンが多量に含まれることは有効に
防止されることになり、他方汚泥Aの貯溜によつ
てベルトプレス脱水機の稼動を、夜間、休日にお
いては停止させることが可能となるからである。
下記表はCa塩を添加して汚泥A,Bを36時間
貯溜した場合の結果を示している。[Table] As is clear from the above table, compared to when sludge A is dehydrated alone, when sludge A and B are combined and treated, the time required for dewatering treatment, the moisture content of the cake, etc. Recognized as excellent. In addition, in Example 1 shown in FIG. 1, the sludge obtained from the mechanical thickener is immediately fed to the belt press machine without being stored on the way, thereby reducing the amount of phosphorus in the liquid due to the emergence of an anaerobic state. It is desirable to prevent the release of sludge into the sludge as much as possible, and therefore it is better to combine the initial settling sludge B as much as possible immediately before the dewatering process, but in order to simplify the refining operation by adding a polymer flocculant In this case, the combined sludge A and B may be stirred in one tempering tank, and in this case as well, sludge treatment can be carried out with the amount of regressed phosphorus kept within a range that does not cause any practical problems. Example 2 In the present Example 2 shown in FIG. 2, the thickened sludge A that was rapidly concentrated using the mechanical thickener 7 compared to that in FIG. 1 was stored in a storage tank 8', and a predetermined amount of Ca salt was added. A further feature is that the initial settling sludge B is merged into this storage tank 8'. Therefore, only one refining tank 10 is provided for the combined sludges A and B. According to such a configuration, it is possible to secure the advantages of sludge treatment shown in FIG. 1 and realize a more practically excellent sludge treatment facility. In other words, even if an anaerobic condition develops in the storage tank 8' due to sludge retention for a long time, and phosphorus is released from the sludge into the liquid, this phosphorus is fixed by the added Ca salt and dewatering takes place. This will effectively prevent large amounts of phosphorus from being contained in the desorbed water S * during treatment, and on the other hand, the operation of the belt press dewatering machine will be stopped at night and on holidays due to the accumulation of sludge A. This is because it becomes possible.
The table below shows the results when sludge A and B were stored for 36 hours with addition of Ca salt.
【表】
なお、Ca塩添加の場合には、比較的脱水処理
に時間のかかるフイルタープレス脱水機を使用す
ることも可能である。
(発明の効果)
以上説明したように、本発明法によれば、A/
O法に従つた二次処理工程をもつ汚水処理系にお
いて、余剰汚泥中のリンを放出させることなく濃
縮脱水が可能となるため、汚水処理系へのリン回
帰が大幅に低減され、A/O法の二次処理工程の
機能を充分発揮させることが可能となり、しか
も、機械濃縮機を用いた迅速濃縮の効果を充分発
揮させ、かつこれが近時汎用化されつつある高分
子凝集剤の調質処理を伴つた脱水処理と組合せて
用いられる場合の問題点も、初沈汚泥との合流と
いう工夫により効果的に解消することができるな
ど、その有用性は極めて大なるものである。
なお、本発明法は、付随的効果として、脱水処
理された余剰汚泥が高リン含有のものであるた
め、汚泥再利用の一つであるコンポスト化におい
て肥料効果の高いものが得られる利点ももつてい
る。[Table] In addition, in the case of adding Ca salt, it is also possible to use a filter press dehydrator, which takes a relatively long time to dehydrate. (Effect of the invention) As explained above, according to the method of the present invention, A/
In sewage treatment systems that have a secondary treatment process in accordance with the O method, it is possible to concentrate and dehydrate excess sludge without releasing phosphorus, which greatly reduces phosphorus return to the sewage treatment system and improves A/O This makes it possible to fully utilize the functions of the secondary treatment process of the method, and also to fully demonstrate the effects of rapid concentration using a mechanical concentrator. Its usefulness is extremely great, as the problems that arise when it is used in combination with dewatering treatment can be effectively resolved by combining it with the initial settling sludge. Additionally, the method of the present invention has the additional advantage that, since the surplus sludge that has been dehydrated contains high phosphorus, it can provide a highly effective fertilizer in composting, which is one of the ways to reuse sludge. ing.
図面第1図は本発明の実施例1のフローを示す
図、第2図は同実施例2のフローを示す図であ
る。
1……初沈、2……二次処理工程設備、3……
嫌気槽、4……好気槽、5……流出渠、6……終
沈、7……機械濃縮機、8……クツシヨンタン
ク、8′……貯溜槽、9,14……ポンプ、10,
15……調質槽、11……混合槽、12……ベル
トプレス脱水機、13……濃縮槽。
FIG. 1 is a diagram showing the flow of the first embodiment of the present invention, and FIG. 2 is a diagram showing the flow of the second embodiment. 1... Initial settling, 2 ... Secondary treatment process equipment, 3...
Anaerobic tank, 4...Aerobic tank, 5...Outlet drain, 6...Final sedimentation, 7...Mechanical thickener, 8...Cushion tank, 8'...Storage tank, 9, 14...Pump, 10,
15... Tempering tank, 11... Mixing tank, 12... Belt press dehydrator, 13... Concentrating tank.
Claims (1)
を嫌気槽−好気槽の順に通してリンを汚泥中に蓄
積させる二次処理の工程をもつ汚水処理法におい
て、前記好気槽出口混合液の一部を、直接、遠心
型又は過型機械濃縮機で迅速濃縮した濃縮汚泥
Aと、前記最初沈澱池からの引抜汚泥Bとを、合
流させた後速やかに脱水処理の工程に送給させる
と共に、機械濃縮後の脱水前処理として高分子凝
集剤により調質処理することを特徴とする汚泥の
処理方法。 2 最初沈澱池引抜汚泥Bは、濃縮槽を経たもの
であることを特徴とする特許請求の範囲第1項に
記載した汚泥の処理方法。 3 最初沈澱池による一次処理の次段に、被処理
水を嫌気槽−好気槽の順に通してリンを汚泥中に
蓄積させる二次処理の工程をもつ汚水処理法にお
いて、前記好気槽出口混合液の一部を、直接、遠
心型又は過型機械濃縮機で迅速濃縮した濃縮汚
泥Aと、前記最初沈澱池からの引抜汚泥Bとを、
合流させた後脱水処理の工程に送給させると共
に、脱水前処理として高分子凝集剤により調質処
理する方法であつて、前記濃縮汚泥Aは、前記汚
泥Bとの合流時又は合流前においてCa塩の添加
を条件として貯溜することを特徴とする汚泥の処
理方法。 4 最初沈澱池引抜汚泥は、濃縮槽を経たもので
あることを特徴とする特許請求の範囲第3項に記
載した汚泥の処理方法。[Scope of Claims] 1. A sewage treatment method having a secondary treatment step in which the water to be treated is passed through an anaerobic tank and an aerobic tank in order to accumulate phosphorus in the sludge after the primary treatment in a sedimentation tank, Thickened sludge A, which is obtained by directly concentrating a part of the mixed liquid at the outlet of the aerobic tank using a centrifugal or cross-type mechanical thickener, and sludge B drawn from the first settling tank are combined and then quickly dehydrated. A method for treating sludge, characterized by feeding the sludge to a treatment process and subjecting it to tempering treatment using a polymer flocculant as a pretreatment for dehydration after mechanical concentration. 2. The sludge treatment method as set forth in claim 1, wherein the sludge B initially drawn from the sedimentation tank has passed through a thickening tank. 3 In a sewage treatment method that has a secondary treatment process in which the water to be treated is passed through an anaerobic tank and an aerobic tank in order to accumulate phosphorus in the sludge after the primary treatment in the initial settling tank, the aerobic tank outlet Thickened sludge A, which is a part of the mixed liquid, is quickly concentrated directly with a centrifugal or cross-type mechanical thickener, and sludge B drawn from the first settling tank,
This is a method in which the concentrated sludge A is fed to a dewatering process after being combined, and is subjected to tempering treatment using a polymer flocculant as a pre-dehydration treatment, wherein the thickened sludge A is freed from Ca at the time of or before joining with the sludge B. A sludge treatment method characterized by storing sludge with the addition of salt. 4. The sludge treatment method as set forth in claim 3, wherein the sludge initially drawn from the sedimentation tank is passed through a thickening tank.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58234794A JPS60129193A (en) | 1983-12-13 | 1983-12-13 | Treatment of sludge |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58234794A JPS60129193A (en) | 1983-12-13 | 1983-12-13 | Treatment of sludge |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60129193A JPS60129193A (en) | 1985-07-10 |
| JPH0420676B2 true JPH0420676B2 (en) | 1992-04-06 |
Family
ID=16976491
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58234794A Granted JPS60129193A (en) | 1983-12-13 | 1983-12-13 | Treatment of sludge |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60129193A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008080310A (en) * | 2006-09-29 | 2008-04-10 | Kurita Water Ind Ltd | Sludge dewatering method |
| JP6038679B2 (en) * | 2013-02-14 | 2016-12-07 | メタウォーター株式会社 | Sludge treatment system |
| JP6664251B2 (en) * | 2016-03-28 | 2020-03-13 | 株式会社北▲りょう▼ | Sludge dewatering method and sludge dewatering device |
-
1983
- 1983-12-13 JP JP58234794A patent/JPS60129193A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60129193A (en) | 1985-07-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3473328B2 (en) | Biological dephosphorization equipment | |
| JP3368938B2 (en) | Wastewater treatment method and apparatus | |
| JP3844347B2 (en) | Method and apparatus for removing and recovering phosphorus from organic wastewater | |
| JPS61257300A (en) | Sludge dewatering equipment | |
| JPH0420676B2 (en) | ||
| JP2796909B2 (en) | Wastewater treatment method | |
| JP3509169B2 (en) | Dewatering method by sludge granulation and concentration | |
| JP2936938B2 (en) | Treatment method of human waste and septic tank sludge | |
| JP3168608B2 (en) | Sludge treatment equipment | |
| JPH04131195A (en) | Device and method for treating sludge | |
| JP3401881B2 (en) | Method for washing and concentration of digested sludge and washing concentrate | |
| JPH0137196B2 (en) | ||
| JP3961246B2 (en) | Method and apparatus for treating organic wastewater | |
| JP2007050387A (en) | Organic waste liquid treatment equipment | |
| JP2002316191A (en) | Method and apparatus for treating organic foul water | |
| JPS60206498A (en) | Treatment of excretion sewage | |
| JPH0649197B2 (en) | Organic wastewater treatment method | |
| JPH06170398A (en) | Treatment of sludge containing blast furnace water slag in activated sludge treatment | |
| JP3420777B2 (en) | Aluminum insolubilization method | |
| JPH0416239B2 (en) | ||
| JP2779128B2 (en) | Method and apparatus for treating sewage sludge and its separated liquid | |
| JP2007050386A (en) | Organic waste liquid treatment equipment | |
| JP2008080310A (en) | Sludge dewatering method | |
| JPH0317932Y2 (en) | ||
| JPS596986A (en) | Treatment of night soil-type filthy water |