JPS643558B2 - - Google Patents
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- Publication number
- JPS643558B2 JPS643558B2 JP8453580A JP8453580A JPS643558B2 JP S643558 B2 JPS643558 B2 JP S643558B2 JP 8453580 A JP8453580 A JP 8453580A JP 8453580 A JP8453580 A JP 8453580A JP S643558 B2 JPS643558 B2 JP S643558B2
- Authority
- JP
- Japan
- Prior art keywords
- tank
- aerobic
- aeration tank
- anaerobic
- supplied
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000005273 aeration Methods 0.000 claims description 56
- 239000007788 liquid Substances 0.000 claims description 31
- 238000003756 stirring Methods 0.000 claims description 28
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 25
- 239000001301 oxygen Substances 0.000 claims description 25
- 229910052760 oxygen Inorganic materials 0.000 claims description 25
- 239000007789 gas Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 239000010815 organic waste Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 4
- 241000894006 Bacteria Species 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000010802 sludge Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 12
- 239000010800 human waste Substances 0.000 description 12
- 238000012545 processing Methods 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 8
- 230000007423 decrease Effects 0.000 description 6
- 238000010790 dilution Methods 0.000 description 6
- 239000012895 dilution Substances 0.000 description 6
- 230000001546 nitrifying effect Effects 0.000 description 6
- 238000004062 sedimentation Methods 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 210000002700 urine Anatomy 0.000 description 5
- -1 Ammonia ions Chemical class 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 239000000852 hydrogen donor Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000005416 organic matter Substances 0.000 description 3
- 125000001477 organic nitrogen group Chemical group 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- 239000002351 wastewater Substances 0.000 description 3
- VTEIFHQUZWABDE-UHFFFAOYSA-N 2-(2,5-dimethoxy-4-methylphenyl)-2-methoxyethanamine Chemical compound COC(CN)C1=CC(OC)=C(C)C=C1OC VTEIFHQUZWABDE-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000003113 dilution method Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000029058 respiratory gaseous exchange Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- JVMRPSJZNHXORP-UHFFFAOYSA-N ON=O.ON=O.ON=O.N Chemical compound ON=O.ON=O.ON=O.N JVMRPSJZNHXORP-UHFFFAOYSA-N 0.000 description 1
- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 description 1
- 241001148470 aerobic bacillus Species 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000020681 well water Nutrition 0.000 description 1
- 239000002349 well water Substances 0.000 description 1
Landscapes
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
Description
本発明は生物分解可能な有機物と共にアンモニ
ア性窒素(以下NH4 +−Nと記す)及び含窒素有
機物を含む有機性廃液の経済的に効率よく安定し
た処理水質を得る脱窒素処理法に関する。
有機性廃液の脱窒素処理に関してはBOD及び
窒素濃度の濃いし尿について既に多くの実装置が
稼動しその中でも硝化液循環法が主流となつてい
る。
有機性廃液中のアンモニアイオン(NH4 +)と
含窒素有機化合物から生成されたNH4 +は硝化を
行う為の好気性第1曝気槽において亜硝酸菌によ
り亜硝酸イオン(NO2 -)に
NH4 ++1.5O2→NO2 -+H2O+H+
NO2 -は硝酸菌により硝酸イオン(NO3 -)に
酸化される。
NO2 -+0.5O2→NO3 -
脱窒素を行う為の嫌気性撹拌槽では脱窒菌は
NO2 -ないしNO3 -を水素受容体として下記のよ
うな呼吸活動をする。
NO2 -を利用した呼吸
2HO2 -+6(H)→N2+2OH-+2H2O
NO3 -を利用した呼吸
2NO3 -+10(H)→N2+2OH-+4H2O
硝化液循環法の利点は好気性第1曝気槽で生成
するNO2 -NO3 -をこの槽の前に設置した嫌気性
第1撹拌槽に循環し、NO2 -、NO3 -を還元する
為の水素供与体として供給有機性廃液中のBOD
成分を利用することにある。この結果循環
NO2 -、NO3 -に見合う供給有機性廃液中のBOD
が最初に流入する嫌気性第1撹拌槽で除去される
為続く好気性第1曝気槽におけるBOD除去量は
減少し、従つて供給酸素量も削減できる。さらに
好気性第1曝気槽の後に続く嫌気性第2撹拌槽に
おける水素供与体としての新たな有機物の供給量
を削減できる。又好気性第1曝気槽では硝化に伴
うPH低下防止の為アルカリ剤を供給するが嫌気性
第1撹拌槽へ循環し脱窒素することにより再びア
ルカリが遊離するから供給アルカリ量も減少す
る。
硝化に伴う中和
NH4OH+2O2+NaOH→NaNO3+3H2O
脱窒に伴うアルカリの遊離
2NaNO3+5(H2)→N2+2NaOH+4H2O
しかしこれまでは硝化液循環法において好気性
第1及び第2曝気槽に開放型空気曝気方式を採用
している為以下のような欠点を有している。
すなわち有機性廃液中の大部分のBODが嫌気
性性第1撹拌槽で除去されたとしてもBOD1gの
除去の為に必要酸素量は約1g必要であるが下式
NH4 ++40→NO3 -+H2O+2H+
の如くNH4−H1g当りの必要酸素量は4.6gであ
り例えば、し尿についてBOD:T−KN=12000
mg/:4500mg/とすれば(T−KNとは有機
体窒素とNH4−Nの和を言う)硝化だけでこれ
までのBOD除去のみに要した酸素量の約1.5倍も
必要となる。
従つて高負荷処理では酸素供給律速となり特に
負荷変動の大きな廃液に対しては安定した処理が
望めず槽容積が大となる為多大な建設費を要す
る。さらに硝化菌はBOD酸化菌よりも高度の好
気性菌とされている為BOD除去のみの場合では
曝気槽中の酸素濃度(以下DOという)は通常0.5
mg/以上で十分であるが硝化の為には一般的に
DO2mg/以上に維持することが必要とされ所
要供給空気量は増加するから前述のように負荷変
動を考慮すると高負荷処理では安定した処理が期
待できなくなる。
又、し尿処理の窒素除去の場合厚生省「構造指
針」では10倍希釈処理が標準であるが、希釈用水
の節減からさらに低希釈、無希釈処理の検討がさ
れている現状にある。低希釈処理では液比重が高
くなり、溶解物質の影響等から、高負荷に伴う曝
気空気量の増加は汚泥フロツクの破壊による処理
水質の悪化、槽内の発泡に対する消泡水量の増大
など維持管理が煩雑になりかつ負荷変動に対応し
た安定な処理が困難となる。
一般に細菌は温度が低下するとその活性は低下
するが硝化菌は他の好気性菌(BOD酸化菌)や
脱窒素菌に比して成長速度が特に遅い為、冬季に
おける硝化菌の活性度が好気性第1曝気槽の容積
を律することになる。従来の空気曝気法は解放式
曝気槽である為熱の放散が大きく、冬季の水温の
低下により処理効率が低下する為槽容積が大とな
り建設費を高めている。
本発明は上述のような従来の欠点を改良し、経
済的に安価な設備により良好な処理水質が安定し
て得られる有機性廃液の処理法を提供することを
目的とするものである。即ち本発明は有機性廃液
を嫌気性第1撹拌槽、好気性第1曝気槽、嫌気性
第2撹拌槽、好気性第2曝気槽の順に構成され、
さらに好気性第1曝気槽より流出する混合液の一
部を嫌気性第1撹拌槽に循環する装置で処理する
に際し、好気性第1曝気槽、好気性第2曝気槽を
密閉槽とし、好気性第1曝気槽より酸素富化ガス
を供給し、その排ガスを好気性第2曝気槽で再利
用して処理することを特徴とする有機性廃液の脱
窒素処理方法にある。
本発明は、し尿、化学工業排水、余剰汚泥熱分
解処理液のようなBOD、有機体窒素、アンモニ
ア性窒素、が共に濃厚な有機性廃液に特に有効に
用いられる。
処理すべき有機性廃液6は嫌気性第1撹拌槽
1、好気性第1曝気槽2、嫌気性第2撹拌槽3、
好気性第2曝気槽4、固液分離槽5の順よりなる
処理工程を通し、固液分離槽5の分離液を処理水
として放流する。
好気性第1曝気槽2と好気性第2曝気槽4は密
閉式とし両槽は好気性槽連通管11により気相部
を連通し、さらに嫌気性第1撹拌槽1へ汚泥返送
路9を介し、固液分離槽分離汚泥の返送、混合液
循環路8を介し好気性第1曝気槽混合液の循環を
行い嫌気的雰囲気下において有機性廃液と接触混
合せしめる、好気性曝気槽の酸素源として酸素濃
度50%以上の酸素富化ガスを好気性第1曝気槽に
供給し、この排出ガスは前述の配管により好気性
第2曝気槽に供給し、ここでの酸素源として再利
用する。好気性第1曝気槽排出ガスの酸素濃度は
21%以上、好ましくは30%以上とし、槽内の溶存
酸素濃度は6mg/以上に維持する。これは供給
酸素富化ガスの効率よい利用、負荷変動に対する
処理の安定性、余剰汚泥の減少、汚泥の沈降性の
向上、曝気用動用の効率から重要である。
さらに希釈、消泡を目的として工業用水や井戸
水を希釈水12として好気性第1曝気槽に供給
し、嫌気性第2撹拌槽における脱窒素の為の水素
供与体としてメタノール、エタノール、酢酸のよ
うな安価に入手できる窒素を含まない有機化合物
を窒素不含有機物供給管7から供給する。
さらに好気性第1曝気槽における硝化に最適な
PH域を維持する為にアルカリ剤を供給することが
ある。これは処理対象廃液のT−KN、BOD濃
度、PH緩衝性、負荷等により異なるが、本発明の
方法によるし尿の処理の場合には、アルカリ剤の
使用は不要か使用しても極めて少量である。
本発明により次のごとく従来法の欠点を解消
し、経済的に安価な設備により良好な処理水質を
安定して得ることが可能となつた。好気性第1曝
気槽を密閉式とし酸素富化ガスを供給することに
より従来法より高DOを無理なく安定して維持で
き処理において酸素供給律速になることなく、活
性汚泥フロツク内部まで酸素が浸透し、好気状態
を維持するので処理効率が増し高負荷処理が可能
となり負荷変動に対しても安定した処理ができ
る。同様な理由で高い活性汚泥濃度を維持できる
から槽容積当りの処理効率が増大する。
酸素富化ガスの使用により従来法より気相酸素
濃度が高くなる為に槽内混合液に対する酸素の溶
解推進力が高くなり、供給ガス量の減少、曝気の
為の所要動力が小となる為高負荷に対しても汚泥
フロツクの破壊防止、し尿の低希釈処理の例にお
ける発泡防止が可能となる。
硝化液循環法ではBOD酸化菌、硝化菌、脱窒
素菌が混合系として各槽を循環している。この方
法で集積培養される脱窒素菌は通性嫌気性菌であ
るが、処理すべき廃液中のBOD成分は嫌気性第
1撹拌槽で大部分除去される為、脱窒素菌は好気
性第1曝気槽ではごく低負荷で高DO域を通過す
ることになり、従つて好気性消化が進行する。脱
窒素菌は硝化菌よりその増殖速度は大きいから脱
窒素菌の減少は系内の硝化菌の比を増加させ、硝
化速度が律速となる本方法にとつて好都合であ
り、併せて余剰汚泥の減少という利点を生ずる。
好気性第2曝気槽は嫌気性第2撹拌槽における
脱窒素処理の際発生するN2ガスの脱気による沈
降性の促進、残存BODの除去を目的として設置
されているが高DOを維持することによりさらに
沈降性が向上することが知られている。本発明に
よれば酸素濃度21%以上の好気性第1撹拌槽排ガ
スの利用により高DOが容易に維持できる為従来
法に較べ槽容積の縮少、沈降性の向上、水質の安
定化が経済的に達成できる。
次に実施例をあげ、本発明を更に詳細に説明す
る。
実施例及び比較例
BOD、有機性窒素、NH4−Nが濃厚でかつ負
荷変動の大きな有機性廃液の代表として、し尿を
取り上げ表−1に実施例と比較例を示す。
実施例、比較例共、供給し尿は、ドラムスクリ
ーンによる除渣し尿を、T−KNで約450mg/
に調製して供給した。
実施例は好気性第1、第2曝気槽に純酸素を供
給しDOを10mg/に調節、槽内MLSSは約6000
mg/好気性第1曝気槽より嫌気性第1撹拌槽へ
の循環量は供給し尿量の5倍量とした。各槽容積
比は本発明による方法において最も効率が良いと
確認された容積比、すなわち実施例に示すような
嫌気性第1撹拌槽:好気性第1曝気槽:嫌気性第
2撹拌槽=1:2:1を採用した。
比較例は従来の空気曝気法の例より最も一般的
な槽容積比として表ー1のように各槽容積を採用
した。DOは好気性第1曝気槽で約3mg/、好
気性第2曝気槽で約5mg/であつた。槽内
MLSSは約4000mg/、好気性第1曝気槽混合液
の循環量は供給し尿量の5倍量とした。
なお、実施例、比較例共嫌気性第2撹拌槽流入
亜硝酸窒素(NO2 -−N)と硝酸窒素(NO3 -−
N)との和の3倍量のメタノールを水素供与体と
して供給した。好気性第1曝気槽のPHコントロー
ルは各例とも行つていない。又実験温度は各例共
25℃にコントロールした。
実験は各例共槽容積、MLSSを一定とし供給し
尿量を一定期間毎に段階的に増加させ、その処理
水の分析を行つた。
表−1に示した値は処理水BOD30mg/以下
でかつ脱窒素処理が安定して行なわれる最高の条
件とその結果を示している。
嫌気性第1撹拌槽のBOD容積負荷は実施例で
は8.2KgBOD/m3日で比較例の1.25KgBOD/m3日
の約6倍の高負荷処理が達成できる。
好気性第1曝気槽におけるT−KN容積負荷は
実施例では1.2KgT−KN/m3日で比較例の0.4Kg
T−KN/m3日の約3倍の高負荷処理が達成でき
る。
嫌気性第2撹拌槽は各例共若干余裕のある大き
さを採用しているが、実施例では比較例の1/2の
槽容積となつている。
好気性第2曝気槽では実施例は比較例の数分の
1の滞留時間においても同等以上の効果を発揮し
ている。
MLSSは実施例では約6000mg/で比較例では
約4000mg/と低いのは活性汚泥の沈降性が劣る
為にこれ以上の濃度では固液分離槽での汚泥の溢
流、返送汚泥濃度の低下による各槽内濃度の低下
を来たす事等による。実施例では好気性曝気槽に
おける酸素曝気において高DO処理される為に沈
降性のよい活性汚泥が得られ、高いMLSS濃度を
維持できる。この結果が前述のような実施例の高
負荷処理の要因となつている。
以上のように本発明の方法によれば処理が安定
し、かつ良好な処理水質が得られる事が明らかで
ある。
換言すれば、供給し尿水質は各例共ほゞ一定で
あるから供給し尿当りの各槽容積の計は実施例で
は総容積/供給し尿量=12.3/16=0.77、比較例
では総容積/供給し尿量=18.5/5=3.7となり
実施例では比較例の約1/5の総容積で同等以上の
良好な処理水が得られる事になる。
The present invention relates to a denitrification treatment method for economically efficient and stable treatment of organic wastewater containing biodegradable organic matter, ammonia nitrogen (hereinafter referred to as NH 4 + -N), and nitrogen-containing organic matter. Regarding the denitrification treatment of organic waste liquid, many actual devices are already in operation for BOD and human waste with high nitrogen concentration, and among them, the nitrification liquid circulation method is the mainstream. Ammonia ions (NH 4 + ) in organic wastewater and NH 4 + generated from nitrogen-containing organic compounds are converted to nitrite ions (NO 2 - ) by nitrite bacteria in the first aerobic aeration tank for nitrification. NH 4 + +1.5O 2 →NO 2 - +H 2 O+H + NO 2 - is oxidized to nitrate ions (NO 3 - ) by nitric acid bacteria. NO 2 - +0.5O 2 →NO 3 - In the anaerobic stirring tank for denitrification, denitrifying bacteria
It performs the following respiratory activities using NO 2 - or NO 3 - as a hydrogen acceptor. Respiration using NO 2 - 2HO 2 - +6 (H) → N 2 +2OH - +2H 2 O Respiration using NO 3 - 2NO 3 - +10 (H) → N 2 +2OH - +4H 2 O Advantages of the nitrified fluid circulation method The NO 2 - NO 3 - generated in the first aerobic aeration tank is circulated to the first anaerobic stirring tank installed in front of this tank, and used as a hydrogen donor to reduce NO 2 - and NO 3 - . BOD in feed organic waste liquid
It consists in using the ingredients. This results in a cycle
BOD in feed organic wastewater commensurate with NO 2 - , NO 3 -
Since the BOD is removed in the first anaerobic stirring tank into which it first flows, the amount of BOD removed in the subsequent first aerobic aeration tank is reduced, and the amount of oxygen supplied can also be reduced. Furthermore, the amount of new organic matter supplied as a hydrogen donor in the second anaerobic stirring tank following the first aerobic aeration tank can be reduced. Further, in the aerobic first aeration tank, an alkaline agent is supplied to prevent the pH from decreasing due to nitrification, but the alkali is liberated again by being circulated to the anaerobic first stirring tank and denitrified, so the amount of alkali supplied also decreases. Neutralization due to nitrification NH 4 OH + 2O 2 +NaOH→NaNO 3 +3H 2 O Release of alkali due to denitrification 2NaNO 3 +5(H 2 )→N 2 +2NaOH+4H 2 O However, until now, aerobic primary and Since the second aeration tank uses an open air aeration system, it has the following drawbacks. In other words, even if most of the BOD in the organic waste liquid is removed in the first anaerobic stirring tank, the amount of oxygen required to remove 1g of BOD is approximately 1g, but the following formula: NH 4 + +40→NO 3 - +H 2 O + 2H + The required amount of oxygen per 1g of NH 4 -H is 4.6g. For example, for human waste, BOD: T - KN = 12000
mg/: 4500 mg/ (T-KN refers to the sum of organic nitrogen and NH 4 -N), nitrification alone will require about 1.5 times the amount of oxygen required for BOD removal alone. Therefore, in high-load processing, oxygen supply becomes rate-limiting, and stable processing cannot be expected, especially for waste liquid with large load fluctuations, and the tank volume becomes large, requiring a large amount of construction cost. Furthermore, nitrifying bacteria are considered to be more highly aerobic than BOD oxidizing bacteria, so when only BOD removal is being performed, the oxygen concentration (hereinafter referred to as DO) in the aeration tank is usually 0.5.
mg/or more is sufficient, but generally for nitrification
Since it is necessary to maintain DO at 2 mg/ or more and the required amount of supplied air increases, stable processing cannot be expected in high-load processing when load fluctuations are taken into account as described above. In addition, in the case of nitrogen removal during human waste treatment, the Ministry of Health and Welfare's ``Structural Guidelines'' states that a 10-fold dilution process is standard, but in order to save water for dilution, even lower dilution or no-dilution processes are currently being considered. In low dilution treatment, the specific gravity of the liquid becomes high, and due to the influence of dissolved substances, the increase in the amount of aeration air associated with high loads will lead to deterioration of treated water quality due to destruction of sludge flocs, and maintenance management such as increasing the amount of defoaming water to prevent foaming in the tank. This makes processing complicated and makes it difficult to perform stable processing in response to load fluctuations. In general, the activity of bacteria decreases as the temperature decreases, but the growth rate of nitrifying bacteria is particularly slow compared to other aerobic bacteria (BOD oxidizing bacteria) and denitrifying bacteria, so the activity of nitrifying bacteria in winter is favorable. This will control the volume of the first aeration tank. Conventional air aeration methods use open aeration tanks, which dissipate a large amount of heat, and lower water temperatures in winter reduce treatment efficiency, resulting in larger tank volumes and higher construction costs. It is an object of the present invention to improve the above-mentioned conventional drawbacks and to provide a method for treating organic waste liquid that can stably obtain good treated water quality using economically inexpensive equipment. That is, in the present invention, the organic waste liquid is constructed in the order of an anaerobic first stirring tank, an aerobic first aeration tank, an anaerobic second stirring tank, and an aerobic second aeration tank,
Furthermore, when a part of the liquid mixture flowing out from the first aerobic aeration tank is processed by a device that circulates it to the first anaerobic stirring tank, the first aerobic aeration tank and the second aerobic aeration tank are closed tanks. A method for denitrifying organic waste liquid, characterized in that oxygen-enriched gas is supplied from a first aerobic aeration tank, and the exhaust gas is reused and treated in a second aerobic aeration tank. The present invention is particularly effectively used for organic waste liquids that are rich in BOD, organic nitrogen, and ammonia nitrogen, such as human waste, chemical industrial wastewater, and surplus sludge thermally decomposed liquid. The organic waste liquid 6 to be treated is divided into a first anaerobic stirring tank 1, a first aerobic aeration tank 2, a second anaerobic stirring tank 3,
The separated liquid in the solid-liquid separation tank 5 is discharged as treated water through a treatment process consisting of the second aerobic aeration tank 4 and the solid-liquid separation tank 5 in this order. The first aerobic aeration tank 2 and the second aerobic aeration tank 4 are of a closed type, and the gas phase portions of both tanks are communicated through an aerobic tank communication pipe 11, and a sludge return path 9 is connected to the first anaerobic stirring tank 1. The oxygen source for the aerobic aeration tank, which returns the separated sludge to the solid-liquid separation tank and circulates the mixed liquid in the first aerobic aeration tank through the mixed liquid circulation path 8 to contact and mix it with the organic waste liquid in an anaerobic atmosphere. Oxygen-enriched gas with an oxygen concentration of 50% or more is supplied to the first aerobic aeration tank, and this exhaust gas is supplied to the second aerobic aeration tank through the aforementioned piping and reused as an oxygen source there. The oxygen concentration of the aerobic first aeration tank exhaust gas is
The dissolved oxygen concentration in the tank is maintained at 21% or more, preferably 30% or more, and the dissolved oxygen concentration in the tank is 6 mg/ or more. This is important from the viewpoints of efficient use of supplied oxygen-enriched gas, stability of treatment against load fluctuations, reduction of excess sludge, improvement of sludge settling properties, and efficiency of aeration. Further, for the purpose of dilution and defoaming, industrial water or well water is supplied as dilution water 12 to the first aerobic aeration tank, and methanol, ethanol, acetic acid, etc. are used as hydrogen donors for denitrification in the second anaerobic stirring tank. An inexpensively available nitrogen-free organic compound is supplied from the nitrogen-free organic material supply pipe 7. Furthermore, it is ideal for nitrification in the aerobic first aeration tank.
Alkaline agents may be supplied to maintain the pH range. This varies depending on the T-KN, BOD concentration, PH buffering property, load, etc. of the waste liquid to be treated, but in the case of human waste treatment using the method of the present invention, the use of alkaline agents is unnecessary, or even if used, the amount is extremely small. be. The present invention eliminates the following drawbacks of the conventional method and makes it possible to stably obtain good treated water quality using economically inexpensive equipment. By making the first aerobic aeration tank a closed type and supplying oxygen-enriched gas, a higher DO can be maintained more stably and more easily than with conventional methods. Oxygen penetrates into the inside of the activated sludge flocs without becoming rate-limiting in oxygen supply during treatment. However, since aerobic conditions are maintained, processing efficiency is increased, high-load processing is possible, and stable processing is possible even with load fluctuations. For the same reason, since a high activated sludge concentration can be maintained, the treatment efficiency per tank volume increases. By using oxygen-enriched gas, the gas phase oxygen concentration is higher than in the conventional method, which increases the driving force for oxygen dissolution into the mixed liquid in the tank, reducing the amount of gas supplied and the power required for aeration. It is possible to prevent the destruction of sludge flocs even under high loads, and to prevent foaming in cases of low dilution treatment of human waste. In the nitrification solution circulation method, BOD oxidizing bacteria, nitrifying bacteria, and denitrifying bacteria circulate in each tank as a mixed system. The denitrifying bacteria cultivated in this method are facultative anaerobic bacteria, but since most of the BOD components in the waste liquid to be treated are removed in the anaerobic first stirring tank, the denitrifying bacteria are facultative anaerobic bacteria. In the 1 aeration tank, the high DO region is passed through with a very low load, so aerobic digestion progresses. Since the growth rate of denitrifying bacteria is higher than that of nitrifying bacteria, a decrease in denitrifying bacteria increases the ratio of nitrifying bacteria in the system, which is advantageous for this method in which the nitrification rate is rate-limiting. This gives rise to the advantage of reduction. The second aerobic aeration tank is installed for the purpose of promoting sedimentation and removing residual BOD by degassing the N2 gas generated during denitrification treatment in the second anaerobic stirring tank, but it maintains a high DO. It is known that this further improves sedimentation properties. According to the present invention, a high DO can be easily maintained by using the aerobic first stirring tank exhaust gas with an oxygen concentration of 21% or more, so it is economical to reduce tank volume, improve sedimentation, and stabilize water quality compared to conventional methods. can be achieved. Next, the present invention will be explained in more detail with reference to Examples. Examples and Comparative Examples Table 1 shows examples and comparative examples of human waste as a representative organic waste liquid that is rich in BOD, organic nitrogen, and NH4 -N and has large load fluctuations. In both Examples and Comparative Examples, the human waste to be supplied is approximately 450 mg/kg of human waste removed by a drum screen using T-KN.
It was prepared and supplied. In the example, pure oxygen was supplied to the first and second aerobic aeration tanks and the DO was adjusted to 10mg/, and the MLSS in the tank was approximately 6000.
mg/The amount of urine circulated from the first aerobic aeration tank to the first anaerobic stirring tank was 5 times the amount of urine supplied. The volume ratio of each tank is the volume ratio confirmed to be the most efficient in the method according to the present invention, that is, the first anaerobic stirring tank: the first aerobic aeration tank: the second anaerobic stirring tank = 1 :2:1 was adopted. In the comparative example, the tank volumes shown in Table 1 were adopted as the most common tank volume ratios compared to the conventional air aeration method. DO was approximately 3 mg/in the first aerobic aeration tank and approximately 5 mg/in the second aerobic aeration tank. Inside the tank
The MLSS was approximately 4000 mg/, and the circulating amount of the aerobic first aeration tank mixture was 5 times the amount of supplied urine. In addition, in both Examples and Comparative Examples, nitrite nitrogen (NO 2 - -N) flowing into the anaerobic second stirring tank and nitrate nitrogen (NO 3 - -
Methanol was supplied as a hydrogen donor in an amount three times the amount of methanol (N). PH control of the first aerobic aeration tank was not performed in each case. Also, the experimental temperature was the same for each example.
The temperature was controlled at 25°C. In each experiment, the tank volume and MLSS were kept constant, the urine volume was increased stepwise at regular intervals, and the treated water was analyzed. The values shown in Table 1 indicate the best conditions and results under which the treated water BOD is 30 mg/or less and the denitrification treatment is carried out stably. The BOD volume load of the first anaerobic stirring tank is 8.2 Kg BOD/m for 3 days in the example, which is about 6 times higher than that of the comparative example of 1.25 Kg BOD/m for 3 days. The T-KN volume load in the first aerobic aeration tank was 1.2KgT-KN/m in the example and 0.4Kg in the comparative example in 3 days.
T-KN/m Achieves approximately 3 times higher load processing than 3 days. The second anaerobic stirring tank has a somewhat generous size in each example, but the tank volume in the example is half that of the comparative example. In the aerobic second aeration tank, the Example exhibits the same or better effect even with a residence time that is a fraction of that of the Comparative Example. The MLSS is low at about 6000 mg/in the example and about 4000 mg/in the comparative example because the sedimentation properties of activated sludge are poor, and if the concentration is higher than this, sludge overflows in the solid-liquid separation tank and the concentration of returned sludge decreases. This is due to a decrease in the concentration in each tank. In the example, activated sludge with good sedimentation properties is obtained because high DO treatment is performed during oxygen aeration in an aerobic aeration tank, and a high MLSS concentration can be maintained. This result is a factor in the high-load processing in the embodiments described above. As described above, it is clear that according to the method of the present invention, the treatment is stable and good treated water quality can be obtained. In other words, since the quality of supplied human waste water is almost constant in each case, the total volume of each tank per supplied human waste is: total volume/supplied human urine amount = 12.3/16 = 0.77 in the example, and total volume/supplied in the comparative example. The amount of human waste = 18.5/5 = 3.7, which means that in the example, treated water of the same or higher quality can be obtained with a total volume of about 1/5 of that of the comparative example.
【表】【table】
図面は本発明に係る処理方法の1例を示す説明
図である。
1……嫌気性第1撹拌槽、2……好気性第1曝
気槽、3……嫌気性第2撹拌槽、4……好気性第
2曝気槽、5……固液分離槽、6……有機性廃
液、7……窒素不含有機物供給管、8……混合液
循環路、9……汚泥返送路、10……酸素富化ガ
ス、11……好気性槽連通管、12……希釈水。
The drawing is an explanatory diagram showing an example of a processing method according to the present invention. 1...Anaerobic first stirring tank, 2...Aerobic first aeration tank, 3...Anaerobic second stirring tank, 4...Aerobic second aeration tank, 5...Solid-liquid separation tank, 6... ... Organic waste liquid, 7 ... Nitrogen-free organic material supply pipe, 8 ... Mixed liquid circulation path, 9 ... Sludge return path, 10 ... Oxygen enriched gas, 11 ... Aerobic tank communication pipe, 12 ... diluted water.
Claims (1)
曝気槽、嫌気性第2撹拌槽、好気性第2曝気槽の
順に構成され、さらに好気性第1曝気槽より流出
する混合液の一部を嫌気性第1撹拌槽に循環する
装置で処理するに際し好気性第1曝気槽、好気性
第2曝気槽を密閉槽とし好気性第1曝気槽より酸
素富化ガスを供給し、その排ガスを好気性第2曝
気槽で再利用して処理することを特徴とする有機
性廃液の脱窒素処理方法。1 Organic waste liquid is transferred to the anaerobic first stirring tank and the aerobic first stirring tank.
It is composed of an aeration tank, an anaerobic second stirring tank, and an aerobic second aeration tank in this order, and is further treated with a device that circulates a part of the liquid mixture flowing out from the aerobic first aeration tank to the anaerobic first stirring tank. At this time, the first aerobic aeration tank and the second aerobic aeration tank are sealed tanks, and oxygen-enriched gas is supplied from the first aerobic aeration tank, and the exhaust gas is reused and treated in the second aerobic aeration tank. A method for denitrifying organic waste liquid, characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8453580A JPS5710391A (en) | 1980-06-24 | 1980-06-24 | Treating method for denitrification of organic waste liquid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8453580A JPS5710391A (en) | 1980-06-24 | 1980-06-24 | Treating method for denitrification of organic waste liquid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5710391A JPS5710391A (en) | 1982-01-19 |
| JPS643558B2 true JPS643558B2 (en) | 1989-01-23 |
Family
ID=13833328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8453580A Granted JPS5710391A (en) | 1980-06-24 | 1980-06-24 | Treating method for denitrification of organic waste liquid |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5710391A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6411668U (en) * | 1987-07-10 | 1989-01-20 |
-
1980
- 1980-06-24 JP JP8453580A patent/JPS5710391A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6411668U (en) * | 1987-07-10 | 1989-01-20 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5710391A (en) | 1982-01-19 |
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