JPS6366599B2 - - Google Patents
Info
- Publication number
- JPS6366599B2 JPS6366599B2 JP56010336A JP1033681A JPS6366599B2 JP S6366599 B2 JPS6366599 B2 JP S6366599B2 JP 56010336 A JP56010336 A JP 56010336A JP 1033681 A JP1033681 A JP 1033681A JP S6366599 B2 JPS6366599 B2 JP S6366599B2
- Authority
- JP
- Japan
- Prior art keywords
- tank
- water
- bacteria
- nitrogen
- nitrification
- 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 90
- 241000894006 Bacteria Species 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 40
- 239000012510 hollow fiber Substances 0.000 claims description 21
- 239000012528 membrane Substances 0.000 claims description 21
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 16
- 230000001546 nitrifying effect Effects 0.000 claims description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 239000007789 gas Substances 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- 229910052760 oxygen Inorganic materials 0.000 claims description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 22
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000002351 wastewater Substances 0.000 description 18
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 15
- 229910017604 nitric acid Inorganic materials 0.000 description 15
- 238000000746 purification Methods 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 13
- 239000007788 liquid Substances 0.000 description 13
- 230000008569 process Effects 0.000 description 13
- 229910021529 ammonia Inorganic materials 0.000 description 11
- 239000000126 substance Substances 0.000 description 9
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 8
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000004062 sedimentation Methods 0.000 description 6
- 230000010065 bacterial adhesion Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000000852 hydrogen donor Substances 0.000 description 5
- -1 polytetrafluoroethylene Polymers 0.000 description 5
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 4
- 239000001099 ammonium carbonate Substances 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 235000012501 ammonium carbonate Nutrition 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000007696 Kjeldahl method Methods 0.000 description 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 239000000386 donor Substances 0.000 description 2
- 239000010800 human waste Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 description 2
- 150000002830 nitrogen compounds Chemical class 0.000 description 2
- 125000001477 organic nitrogen group Chemical group 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000009423 ventilation Methods 0.000 description 2
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 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
- 239000001888 Peptone Substances 0.000 description 1
- 108010080698 Peptones Proteins 0.000 description 1
- 239000004698 Polyethylene Substances 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
- 230000001464 adherent effect Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 238000009313 farming Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 235000019319 peptone Nutrition 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- FHSWXOCOMAVQKE-UHFFFAOYSA-N phenylazanium;acetate Chemical compound CC([O-])=O.[NH3+]C1=CC=CC=C1 FHSWXOCOMAVQKE-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/10—Biological treatment of water, waste water, or sewage
Landscapes
- Biological Treatment Of Waste Water (AREA)
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
Description
本発明は生物化学的硝化脱窒法によつて含窒素
化合物を含む水からこれを除去する水の浄化法に
関するものである。
生物学的硝化脱窒法とは水に含まれる有機態窒
素及びアンモニア態窒素を好気的雰囲気下で硝化
細菌の作用により亜硝酸または硝酸に酸化し、次
いでこれ等を嫌気的雰囲気下で水素供与体を加え
脱窒細菌の作用により分子状窒素まで還元する方
法である。ここで云う水素供与体とはメタノー
ル、酢酸、糖類等の有機物質および廃水中に含ま
れる有機物質に由来するBOD源である。また、
これ等の変化は次式で示される。
NH+ 4+1.5O2亜硝酸菌
――――→
NO2+H2O
+2H+
NO- 2+0.5O2硝酸菌
―――→
NO- 3
NO- 3水素供与体脱窒菌
―――→
0.5N2+2H2O
+OH-
NO- 2水素供与体脱窒菌
―――→
0.5N2+H2O
+OH-
有機態窒素はアンモニア態窒素に分解され上記
の反応で分解されるのが一般的である。
従来、このような水の生物化学的な浄化法は好
気的条件下で水中のBODを酸化除去すると共に
アンモニアを亜硝酸または硝酸まで酸化する工程
(硝化処理工程)と嫌気的条件下で亜硝酸または
硝酸を分子状窒素まで還元する工程(脱窒処理工
程)とから成る処理工程を設け、それぞれの工程
ごとに処理槽および沈殿槽を備え、硝化槽でアン
モニアを完全に処理した後に脱窒槽で亜硝酸また
は硝酸を処理する方法である。水中にBOD源を
多量に含む時は硝化喪槽の前にBOD源を酸化除
去する工程(BOD処理工程)が設けられている。
このような浄化法では硝化処理において水中の
アンモニアが亜硝酸または硝酸まで酸化されると
処理槽内のPHが低下するためアルカリ剤を添加し
てPHを調整しなければならない。また、処理槽内
の亜硝酸または硝酸濃度が高くなるとアンモニア
の硝化速度が低下する。このため水中のアンモニ
ア濃度を高くできず、高濃度にアンモニアを含む
水では多量の希釈水が必要となる。一方、脱窒処
理においては脱窒槽に流入する水には有機物質は
殆どないため、亜硝酸または硝酸を分子状窒素ま
で還元するのに水素供与体として窒素原子を含ま
ないメタノール、酢酸、糖類等の有機物質を槽内
に添加しなければならない。
以上このような浄化方法ではアルカリ剤、高価
な有機物質を多量に必要とし、また含窒素化合物
を高濃度に含む水では多量の希釈水が必要となり
運転費が嵩む。多量にBOD源を含む水では硝化
処理工程の前にBOD酸化処理工程を設けなけれ
ばならず処理工程が繁雑となる等の問題点があ
る。
これ等の問題点を解決するために次のような方
法が行なわれている。すなわち、硝化細菌および
脱窒細菌を含む汚泥を浮遊状態で水に接触させる
ことにより硝化処理を行なう際にアンモニア性窒
素の硝化を完全に行なわずに脱窒処理を行ない、
これ等を繰り返して行なうことでアンモニア性窒
素を除去する水の浄化方法である(特開昭50―
38357)。
また、同様な方法を用いて硝化処理と脱窒処理
とを繰り返し行なう際に、脱窒処理に必要な有機
物質として水中に含まれるBOD源を利用するこ
とによりアンモニア性窒素を除去する水の浄化方
法である(遠矢等、用水と廃水151058.1973)。
これ等の浄化方法によつて、硝化処理でのアル
カリ剤の添加量を著しく減少させることができ、
特に後者の方法では脱窒処理する際に添加する有
機物質の添加量を減少、もしくは全く添加せずに
含窒素化合物と共にBOD源をも同時に浄化する
ことができ、この方法は優れたものである。
現在のところ、これ等の浄化方法を実施するに
は硝化槽、脱窒槽、沈殿槽を設け、硝化細菌およ
び脱窒細菌を含む水を硝化槽と脱窒槽間で循環
し、沈殿槽よりこれ等の細菌を返送しながら各々
の槽においてこれ等の細菌を浮遊状態で水と接触
させなければならない。
このため槽内のこれ等の細菌濃度を高くすると
沈殿槽での浄化水と細菌との分離が難かしく、よ
つて槽内にこれ等の細菌を高密度(MLSS10000
mg/以上)に保持することは難かしい。また、
これ等の細菌を含む水を硝化槽と脱窒槽間で循環
するため、これ等の細菌は好気的雰囲気下および
嫌気的雰囲気下に交互におかれることになりよつ
てそれぞれの細菌の機能が充分に発揮されていな
い。
これ等のため処理効率が悪く、負荷変動等によ
り処理が不調になり易く、また運転維持管理に熟
練を要する等の欠点があり、優れた浄化方法が充
分に生かされていない。
本願発明者等はこれ等の欠点を改善すべく鋭意
検討の結果硝化槽中には硝化細菌を、脱窒槽中に
は脱窒細菌を生物支持体に付着した状態で水と接
触させることにより、これ等の細菌を硝化槽と脱
窒槽間で循環せずに水だけを循環することがで
き、また沈殿槽よりこれ等の細菌を返送せずとも
処理槽内にこれ等の細菌を高密度に保持できるこ
とを見い出し、さらに硝化処理における生物支持
体としてその内部より酸素を供給できる多孔質の
中空糸状膜が好都合に用いられることを見い出し
本発明に至つた。
すなわち、本発明は含窒素化合物を含む水を生
物化学的に浄化する方法において槽内に硝化細菌
の支持体として中空糸状膜を充填し、この内部よ
り酸素またはこれを含む気体を通気するようにし
た硝化槽と槽内に脱窒細菌の支持体を充填した脱
窒槽を設け、硝化槽と脱窒槽間で水を循環するこ
とを特徴とする含窒素化合物を含む水の浄化方法
である。
含窒素化合物とは水酸化アンモニウム、炭酸ア
ンモニウム、重炭酸アンモニウ等のアンモニウム
塩、尿素、アミノ酸、タンパク質等の微生物によ
つて加水分解を受け水酸化アンモニウム、炭酸ア
ンモニウム等に変化する化合物であり、含窒素化
合物を含む水としてはアンモニア合成や尿素合成
等の製造工程より排出される廃水、し尿および養
豚廃水等である。これ等の中にはし尿のように含
窒素化合物の他に有機物質に由来するBOD源が
含まれていてもよい。さらに亜硝酸塩、硝酸塩も
含まれていてもよい。
本発明での槽とは第1図に示すように水の流入
口2と流出口3を備えた容器でありその形状は如
何ようなものでもよく、できるだけ流入口と流出
口とは離れていることが望ましい。また硝化細菌
の支持体とは硝化細菌を付着した状態で槽内に保
持するものであり、中空糸状膜4が用いられる。
本発明において使用される中空糸状膜は通常紡
糸可能な高分子材料、例えばポリオレフイン、ハ
ロゲン化ポリオレフイン、ポリアクリロニトリ
ル、芳香族ポリエステル、芳香族ポリアミド等を
中空糸状膜に成型し、延伸処理その他の方法で多
孔化させたもので、一般に、限外過や逆浸透な
どに使用されるものであるが、特に水との接触角
が90゜以上の高分子材料、例えばポリ四弗化エチ
レン、ポリ弗化ビニリデン等のハロゲン化ポリオ
レフイン、ポリプロピレン、ポリエチレン等のポ
リオレフイン等が好都合に用いられる。
中空糸状膜の外径は、0.01〜3mm、好ましくは
0.05〜1mmのもので、気体透過性は乾燥状態にお
いて通常10〜300000/m2,hr,atmのものであ
り、このようなものを適当に用いうる。また中空
糸状膜の壁膜の微細孔は水中の微生物が内部に侵
入し得ない程度に微細であることが好ましく孔径
0.5μ以下のものが好都合に用いられる。
中空糸状膜内部から酸素またはこれを含む気体
を通気するとは中空糸状膜内部に空気または純酸
素あるいは酸素濃度を高めた気体等をたとえば送
気管5で圧入することで行なわれ、これ等の気体
の通気量は中空糸状膜内に加える圧力を適当に変
えることで行なわれる。
本発明において使用される硝化槽とは水中に含
まれるアンモニア性窒素を生物化学的に硝化処理
を行なう処理槽であり、一端または両端を送気源
に接続された多数本からなる中空糸状膜の束を槽
内に均一に充填したものである。ここで云う送気
源とは酸素またはこれを含む気体を送気する装置
またはこれ等の気体を加圧貯留した容器である。
このような硝化槽を用いることの長所は中空糸
状膜を硝化細菌の支持体および酸素供給手段に使
用するため、単位容積当り、非常に大きな細菌付
着面積を存在させることができ、よつて槽内の細
菌濃度が高められる。また水と細菌との接触面積
も大きくできることによつて水と細菌との接触が
よくなる。さらに支持体の内部より均一に酸素が
供給されるため槽内全域にわたつて好気的雰囲気
に保つことができる等である。このような長所に
より硝化処理効率が著しく高くなる。
本発明において使用する脱窒槽は槽内に脱窒細
菌を付着させた状態で保持できるハニカム構造
物、プラスチツク片、糸状物、回転円板、中空糸
状膜等の支持体を充填したもので、槽内の細菌濃
度を高くでき、水と細菌との接触がよく、さらに
付着細菌を嫌気的雰囲気下に保つことができるも
のなら如何ようなものでもよい。また硝化槽で用
いたと同様の中空糸状膜を用いて、中空部よりメ
タンガス、窒素ガス、炭酸ガス等の酸素ガス以外
のガスを供給しても良い。
これ等細菌の支持体を充填した処理槽を用いる
ことの長所は硝化細菌を好気的雰囲気下に、脱窒
細菌を嫌気的雰囲気下に保持できるので充分にそ
の機能が発揮でき、また槽内に細菌を高密度に存
在させることができ、沈殿槽より細菌の返送をせ
ずともよくなることである。これ等の長所によつ
て処理効率が高められ、また運転操作が著しく容
易になる。
また、本発明において硝化槽と脱窒槽間で水を
循環するとは硝化槽の水を脱窒槽に、脱窒槽の水
を硝化槽に輸送することを連続的に繰り返えすこ
とである。水の循環は送液ポンプを用いて行なわ
れその水量は含窒素化合物を含む水を循環水で希
釈した時の窒素源濃度が10〜500mg/程度、好
ましくは20〜100mg/程度になるようにすれば
よい。
このように水の循環を行なうことで硝化槽でア
ンモニアの酸化により生成した亜硝酸または硝酸
は脱窒槽で分子状窒素まで還元され、残存するア
ンモニアおよび新たに含窒素化合物から生成した
アンモニアは再び硝化槽に戻され、亜硝酸または
硝酸に酸化される。また、硝化槽では水のPHは低
下するが、一方脱窒槽では水のPHは上昇するので
両槽間で水を循環することで互に中和されアルカ
リ剤を添加することなく硝化槽の水のPHを7〜8
に保つことができる。また、含窒素化合物を高濃
度に含む水でも循環水で希釈されるため、新たに
希釈水を用いずとも水の浄化が可能である。さら
に、BOD源を含む水の場合、これを脱窒槽に流
入させることにより、亜硝酸または硝酸を還元す
る際の水素供与体として利用することができるだ
けでなくBOD源の処理も同時に行なわれること
になる。
本発明の方法により含窒素化合物を含む水の浄
化を行なう際には初めに硝化槽および脱窒槽内の
生物支持体にそれぞれの機能を有する細菌を付着
形成させる必要がある。
これには硝化槽で空気または純酸素あるいは酸
素濃度を高めた気体を通気しながら、初め低濃度
の含窒素化合物を含む水を処理装置内に循環さ
せ、浄化が進むに従つて含窒素化合物の濃度を高
めた水を循環させるようにする。この水の供給は
BOD源を含む水では脱窒槽に、BOD源を含まな
い水では硝化槽に行なうことが望ましい。
また、水中に含まれる窒素濃度がBOD源濃度
に比較して0.3倍以上高い時は脱窒槽に水素供与
体として含窒素化合物を含まない有機物質を添加
することが望ましい。また、水中に細菌が増殖す
るために必要な栄養塩類が不足している時はこれ
を添加する必要がある。
このようにして約2ケ月程度で細菌の付着形成
が達せられる。各処理槽に種汚泥を添加し、脱窒
槽に硝酸を添加することによりさらに短期間で細
菌の付着形成がなされ好都合である。
こうして形成された付着細菌は高負荷にも、急
激な負荷変動にも安定であり、効率よく水の浄化
を行なうことができる。また、支持体上の細菌層
はある程度以上発達すると表層より細菌塊として
脱落するが、これを沈降性がよく分離除去が容易
である。
本発明では生物支持体を水中に浸漬した状態で
行なつてもよく、または生物支持体表面に水を流
下させて行なつてもよい。さらに各槽ごとに液の
循環を行なつてもよい。
また本発明の方法はそれ自体で優れた水の浄化
能力を有するが他の生物化学的浄化法または化学
的、物理的浄化法等と組合せて使用してもよい。
本発明の方法は含窒素化合物を含む水の浄化に
広く適応でき、浄化効率が高いため装置の小型化
もでき、アルカリ剤の添加を必要とせず、また
BOD源を水素供与体として利用できるため経済
性にも優れている。また、運転操作や維持管理が
容易であるため小規模の水の浄化にも適用しやす
い。
以下に実施例を示す。
実施例 1
第1図、第2図に示したような流入水の入口2
を上部に、流出水の出口3を下部に備えた、縦
0.1m、横0.1m、高さ0.7mの槽1に外径270μ、内
径220μ、長さ1mのポリプロピレン製中空糸状
膜41600本を400本づつに束ね、それぞれの下部
に開口端7、上部に折り曲げ部がくるようにルー
プ状に充填した硝化槽(第1図)および脱窒槽
(第2図)を用いた。硝化槽は上部の折り曲げ部
を上部中空糸状膜支持体6でつるして固定し、下
部の開口端を4本送気管5に接続した。脱窒槽は
上部の折り曲げ部、下部の開口端とも、中空糸状
膜が槽内に均一に分散するように固定した。この
2つの槽を用いて第3図に示すように送液ポンプ
および管を接続した。即ち脱窒槽8の水の出口を
送液管を介して送液ポンプ10の吸入部に接続
し、この吐出部を送液管を介して硝化槽9の水の
入口に接続し、硝化槽の水の出口に接続した送液
管を2つに分け、一方を処理水の流出管12と
し、他方を廃水送液管11に接続し、これを脱窒
槽の水の入口に接続した。
初めに槽内の中空糸状膜を水中に浸漬した後、
各槽に種汚泥を添加し、硝化槽で送気管5より空
気を通気し、両槽間で水を循環しながら、硝酸を
添加した廃水を供給し、脱窒細菌および硝化細菌
の付着形成を図つた。
なお、槽内温度25℃、空気の通気量40/hr、
循環水量/廃水供給量=14、廃水はペプトン、肉
エキス、尿素を主体とした合成廃水を用いた。
細菌の付着形成が進むにつれ硝酸の添加量を減
じ、約1ケ月後には細菌の付着形成は充分になさ
れた。
そこで、廃水の脱窒槽および硝化槽における滞
留時間15hrsで処理を行なつた。廃水、処理水中
のアンモニア態窒素(NH+ 4―N)、有機態窒素
(Org―N)はケルダール法で、亜硝酸態窒素
(NO- 3)、硝酸態窒素(NO- 3―N)は酢酸アニリ
ン法、BODはBODテスター(大洋科学工業KK
製)で行なつた。処理結果を表―1に示す。
The present invention relates to a water purification method for removing nitrogen-containing compounds from water by a biochemical nitrification-denitrification method. Biological nitrification and denitrification method oxidizes organic nitrogen and ammonia nitrogen contained in water to nitrite or nitric acid in an aerobic atmosphere through the action of nitrifying bacteria, and then provides hydrogen to these in an anaerobic atmosphere. In this method, the nitrogen is reduced to molecular nitrogen through the action of denitrifying bacteria. The hydrogen donor referred to here is a BOD source derived from organic substances such as methanol, acetic acid, sugars, and organic substances contained in wastewater. Also,
These changes are shown by the following equation. NH + 4 +1.5O 2Nitrite bacteria――――→ NO 2 +H 2 O +2H + NO - 2 +0.5O 2Nitrate bacteria――――→ NO - 3 NO - 3Hydrogen donor denitrifying bacteria――――→ 0.5N 2 +2H 2 O +OH - NO - 2Hydrogen donor denitrifier ---→ 0.5N 2 + H2O + OH -Organic nitrogen is generally decomposed into ammonia nitrogen and decomposed by the above reaction. be. Traditionally, such biochemical water purification methods have involved a process of oxidizing and removing BOD in water under aerobic conditions and oxidizing ammonia to nitrite or nitric acid (nitrification process), and a process of oxidizing ammonia to nitrite or nitric acid under anaerobic conditions. A treatment process consisting of nitric acid or a process of reducing nitric acid to molecular nitrogen (denitrification process) is provided, and a treatment tank and a precipitation tank are provided for each process, and after the ammonia is completely treated in the nitrification tank, the denitrification tank is installed. This is a method of treating nitrous acid or nitric acid with When water contains a large amount of BOD sources, a process to oxidize and remove the BOD sources (BOD treatment process) is provided before the nitrification tank. In such a purification method, when ammonia in water is oxidized to nitrite or nitric acid during nitrification treatment, the pH in the treatment tank decreases, so an alkaline agent must be added to adjust the pH. Furthermore, when the concentration of nitrite or nitric acid in the treatment tank increases, the nitrification rate of ammonia decreases. For this reason, it is not possible to increase the ammonia concentration in water, and water containing a high concentration of ammonia requires a large amount of dilution water. On the other hand, in denitrification treatment, there are almost no organic substances in the water flowing into the denitrification tank, so methanol, acetic acid, and sugars, which do not contain nitrogen atoms, are used as hydrogen donors to reduce nitrite or nitric acid to molecular nitrogen. of organic material must be added to the tank. As mentioned above, such a purification method requires a large amount of an alkaline agent and an expensive organic substance, and when water contains a high concentration of nitrogen-containing compounds, a large amount of dilution water is required, which increases operating costs. In the case of water containing a large amount of BOD sources, a BOD oxidation treatment process must be performed before the nitrification treatment process, which poses problems such as the treatment process becoming complicated. In order to solve these problems, the following methods have been used. That is, when performing nitrification treatment by bringing sludge containing nitrifying bacteria and denitrifying bacteria into contact with water in a suspended state, denitrification treatment is performed without completely nitrifying ammonia nitrogen,
This is a water purification method that removes ammonia nitrogen by repeating these steps (Japanese Unexamined Patent Application Publication No. 1973-
38357). In addition, when nitrification treatment and denitrification treatment are repeated using the same method, ammonia nitrogen is removed by using the BOD source contained in the water as an organic substance necessary for denitrification treatment. method (Toya et al., Water and Wastewater 15 1058.1973). By using these purification methods, the amount of alkaline agent added during nitrification treatment can be significantly reduced.
In particular, the latter method is excellent because it can simultaneously purify nitrogen-containing compounds and BOD sources without reducing the amount of organic substances added during denitrification treatment or without adding them at all. . Currently, in order to implement these purification methods, a nitrification tank, a denitrification tank, and a sedimentation tank are installed, water containing nitrifying bacteria and denitrification bacteria is circulated between the nitrification tank and the denitrification tank, and water is removed from the sedimentation tank. These bacteria must be brought into contact with the water in suspension in each tank, while returning the bacteria. For this reason, if the concentration of these bacteria in the tank is high, it will be difficult to separate the bacteria from purified water in the sedimentation tank.
mg/or more) is difficult to maintain. Also,
Since water containing these bacteria is circulated between the nitrification tank and the denitrification tank, these bacteria are placed alternately in an aerobic atmosphere and an anaerobic atmosphere, and their functions are affected. It is not fully demonstrated. For these reasons, treatment efficiency is poor, treatment tends to malfunction due to load fluctuations, etc., and there are disadvantages such as requiring skill in operation and maintenance, and excellent purification methods are not fully utilized. In order to improve these drawbacks, the inventors of the present application have made extensive studies and found that by bringing nitrifying bacteria in the nitrification tank and denitrifying bacteria in the denitrification tank into contact with water while attached to a biological support, It is possible to circulate only water without circulating these bacteria between the nitrification tank and the denitrification tank, and it is possible to maintain a high density of these bacteria in the treatment tank without having to send these bacteria back from the sedimentation tank. The present inventors have discovered that a porous hollow fiber membrane capable of supplying oxygen from within can be advantageously used as a biological support in nitrification treatment, leading to the present invention. That is, the present invention is a method for biochemically purifying water containing nitrogen-containing compounds, in which a hollow fiber membrane is filled in a tank as a support for nitrifying bacteria, and oxygen or a gas containing the same is aerated from inside the tank. This method of purifying water containing nitrogen-containing compounds is characterized by providing a nitrification tank and a denitrification tank filled with a support for denitrifying bacteria in the tank, and circulating water between the nitrification tank and the denitrification tank. Nitrogen-containing compounds are compounds such as ammonium salts such as ammonium hydroxide, ammonium carbonate, and ammonium bicarbonate, urea, amino acids, and proteins that undergo hydrolysis by microorganisms and change into ammonium hydroxide, ammonium carbonate, etc. Examples of water containing nitrogen compounds include wastewater discharged from manufacturing processes such as ammonia synthesis and urea synthesis, human waste, and pig farming wastewater. These may include BOD sources derived from organic substances in addition to nitrogen-containing compounds such as human waste. Furthermore, nitrites and nitrates may also be included. The tank in the present invention is a container equipped with an inlet 2 and an outlet 3 for water as shown in FIG. This is desirable. Further, the support for the nitrifying bacteria is a support for holding the nitrifying bacteria in the tank in an attached state, and a hollow fiber membrane 4 is used. The hollow fiber membrane used in the present invention is usually formed from a spinnable polymeric material such as polyolefin, halogenated polyolefin, polyacrylonitrile, aromatic polyester, aromatic polyamide, etc. It is a porous material that is generally used for ultrafiltration and reverse osmosis, but it is especially suitable for polymer materials with a contact angle of 90° or more with water, such as polytetrafluoroethylene, polyfluoroethylene, etc. Halogenated polyolefins such as vinylidene, polyolefins such as polypropylene, polyethylene, etc. are conveniently used. The outer diameter of the hollow fiber membrane is 0.01 to 3 mm, preferably
It is 0.05 to 1 mm and has a gas permeability of usually 10 to 300000/m 2 , hr, atm in a dry state, and such a material can be used appropriately. In addition, the micropores in the wall of the hollow fiber membrane are preferably so small that microorganisms in the water cannot penetrate inside.
Those below 0.5μ are conveniently used. Aerating oxygen or a gas containing oxygen from inside the hollow fiber membrane is carried out by pressurizing air, pure oxygen, or a gas with increased oxygen concentration into the hollow fiber membrane through the air supply pipe 5. The amount of ventilation is controlled by appropriately changing the pressure applied within the hollow fiber membrane. The nitrification tank used in the present invention is a treatment tank that performs biochemical nitrification treatment on ammonia nitrogen contained in water, and consists of a large number of hollow fiber membranes connected at one or both ends to an air supply source. The bundles are filled uniformly into a tank. The air supply source referred to herein is a device for supplying oxygen or a gas containing oxygen, or a container in which such a gas is stored under pressure. The advantage of using such a nitrification tank is that since the hollow fiber membrane is used as a support for nitrifying bacteria and as an oxygen supply means, a very large area of bacteria can be attached per unit volume, and therefore the inside of the tank is bacterial concentration is increased. Furthermore, by increasing the contact area between water and bacteria, contact between water and bacteria can be improved. Furthermore, since oxygen is uniformly supplied from inside the support, an aerobic atmosphere can be maintained throughout the tank. These advantages significantly increase the efficiency of nitrification treatment. The denitrification tank used in the present invention is filled with supports such as honeycomb structures, plastic pieces, threads, rotating discs, and hollow fiber membranes that can hold denitrifying bacteria in a state in which they are attached. Any material may be used as long as it can increase the concentration of bacteria in the container, allow good contact between water and bacteria, and keep attached bacteria in an anaerobic atmosphere. Alternatively, a hollow fiber membrane similar to that used in the nitrification tank may be used to supply gas other than oxygen gas, such as methane gas, nitrogen gas, or carbon dioxide gas, from the hollow portion. The advantage of using a treatment tank filled with these bacterial supports is that nitrifying bacteria can be kept in an aerobic atmosphere and denitrifying bacteria can be kept in an anaerobic atmosphere, so their functions can be fully demonstrated. Bacteria can be present at a high density in the tank, and there is no need to send the bacteria back to the sedimentation tank. These advantages increase processing efficiency and significantly facilitate operation. Further, in the present invention, circulating water between the nitrification tank and the denitrification tank means continuously repeating transporting water from the nitrification tank to the denitrification tank and water from the denitrification tank to the nitrification tank. Water circulation is performed using a liquid pump, and the amount of water is adjusted so that the nitrogen source concentration is about 10 to 500 mg/, preferably about 20 to 100 mg/, when water containing nitrogen compounds is diluted with circulating water. do it. By circulating water in this way, nitrous acid or nitric acid produced by oxidation of ammonia in the nitrification tank is reduced to molecular nitrogen in the denitrification tank, and remaining ammonia and ammonia newly produced from nitrogen-containing compounds are nitrified again. It is returned to the tank and oxidized to nitrite or nitric acid. In addition, in the nitrification tank, the PH of the water decreases, while in the denitrification tank, the PH of the water increases, so by circulating the water between both tanks, the water in the nitrification tank can be neutralized without adding an alkaline agent. pH of 7-8
can be kept. Moreover, since even water containing a high concentration of nitrogen-containing compounds is diluted with circulating water, water can be purified without using new dilution water. Furthermore, in the case of water containing a BOD source, by flowing it into the denitrification tank, it can not only be used as a hydrogen donor when reducing nitrite or nitric acid, but also treat the BOD source at the same time. Become. When purifying water containing nitrogen-containing compounds by the method of the present invention, it is first necessary to attach bacteria having the respective functions to the biological supports in the nitrification tank and the denitrification tank. For this purpose, water that initially contains low concentrations of nitrogen-containing compounds is circulated through the treatment equipment while air, pure oxygen, or gas with increased oxygen concentration is aerated in the nitrification tank, and as the purification progresses, the nitrogen-containing compounds are removed. Circulate highly concentrated water. This water supply is
It is preferable to use a denitrification tank for water that contains a BOD source, and a nitrification tank for water that does not contain a BOD source. Furthermore, when the nitrogen concentration in water is 0.3 times or more higher than the BOD source concentration, it is desirable to add an organic substance that does not contain nitrogen-containing compounds as a hydrogen donor to the denitrification tank. Additionally, when the water lacks the nutrients necessary for bacteria to proliferate, it is necessary to add them. In this way, bacterial adhesion formation is achieved in about two months. By adding seed sludge to each treatment tank and adding nitric acid to the denitrification tank, bacterial adhesion can be formed in a shorter period of time, which is advantageous. The adherent bacteria thus formed are stable even under high loads and rapid load changes, and can efficiently purify water. Furthermore, once the bacterial layer on the support has developed beyond a certain level, it falls off as bacterial lumps from the surface layer, but this has good sedimentation properties and can be easily separated and removed. In the present invention, the biological support may be immersed in water, or water may be allowed to flow down onto the surface of the biological support. Furthermore, the liquid may be circulated for each tank. Further, although the method of the present invention has excellent water purification ability by itself, it may be used in combination with other biochemical purification methods or chemical or physical purification methods. The method of the present invention is widely applicable to the purification of water containing nitrogen-containing compounds, has high purification efficiency, allows for miniaturization of equipment, does not require the addition of alkaline agents, and
It is also economical because the BOD source can be used as a hydrogen donor. In addition, since it is easy to operate and maintain, it is easy to apply to small-scale water purification. Examples are shown below. Example 1 Inlet 2 of inflow water as shown in Figs. 1 and 2
Vertical with water outlet 3 at the top and outlet 3 at the bottom.
41,600 hollow fiber membranes made of polypropylene with an outer diameter of 270μ, an inner diameter of 220μ, and a length of 1m are bundled into 400 bundles in a tank 1 measuring 0.1m, width 0.1m, and height 0.7m, each with an open end 7 at the bottom and an open end 7 at the top. A nitrification tank (Fig. 1) and a denitrification tank (Fig. 2) filled in a loop shape so that the bent portion was located were used. The nitrification tank was fixed by hanging the bent part at the upper part with an upper hollow fiber membrane support 6, and the open ends at the lower part were connected to four air pipes 5. The denitrification tank was fixed at both the bent portion at the top and the open end at the bottom so that the hollow fiber membranes were uniformly dispersed within the tank. Using these two tanks, a liquid pump and pipes were connected as shown in FIG. That is, the outlet of the water in the denitrification tank 8 is connected to the suction part of the liquid feed pump 10 via a liquid feed pipe, and this discharge part is connected to the inlet of the water in the nitrification tank 9 via a liquid feed pipe. The liquid feed pipe connected to the water outlet was divided into two parts, one of which was used as the treated water outflow pipe 12, and the other connected to the waste water liquid feed pipe 11, which was connected to the water inlet of the denitrification tank. After first immersing the hollow fiber membrane in the tank in water,
Seed sludge is added to each tank, air is aerated through the air pipe 5 in the nitrification tank, and while water is circulated between both tanks, wastewater to which nitric acid has been added is supplied to prevent the formation of adhesion of denitrifying bacteria and nitrifying bacteria. Figure. In addition, the temperature inside the tank is 25℃, the air ventilation rate is 40/hr,
Amount of circulating water/amount of wastewater supplied = 14, and synthetic wastewater mainly containing peptone, meat extract, and urea was used as wastewater. As bacterial adhesion formation progressed, the amount of nitric acid added was reduced, and after about one month, sufficient bacterial adhesion formation was achieved. Therefore, the wastewater was treated with a residence time of 15 hours in the denitrification tank and nitrification tank. Ammonia nitrogen (NH + 4 -N) and organic nitrogen (Org -N) in wastewater and treated water are determined by the Kjeldahl method, and nitrite nitrogen (NO - 3 ) and nitrate nitrogen (NO - 3 -N) are determined by the Kjeldahl method. Aniline acetate method, BOD tester (Taiyo Kagaku Kogyo KK)
(manufactured by). The processing results are shown in Table 1.
【表】
実施例 2
実施例と同じ処理槽を用い、第4図に示した処
理装置を用いて廃水の処理を行なつた。即ち硝化
槽9の水の出口を送液管を介して、送液ポンプ1
0の吸入部に接続し、この吐出部を送液管を介し
て脱窒槽8の水の入口に接続し、脱窒槽の水の出
口に接続した送液管を2つに分け、一方を処理水
の流出管12とし、他方を廃水送管11に接続し
これを硝化槽の水の入口に接続した。
脱窒細菌および硝化細菌の付着形成成は実施例
1と同様にして行なつた。但し廃水としては炭酸
アンモニウムを主体とした合成廃水を用い、脱窒
槽にメタノール供給管13よりメタノールを、メ
タノール/窒素=2.5の比率で添加した。
細菌の付着形成後、廃水の脱窒槽、硝化槽にお
ける滞留時間15hrsで処理を行なつた。廃水、処
理水の分析は実施例1と同様にして行なつた。処
理結果を表―2に示す。[Table] Example 2 Using the same treatment tank as in Example, wastewater was treated using the treatment apparatus shown in FIG. 4. That is, the water outlet of the nitrification tank 9 is connected to the liquid feeding pump 1 via the liquid feeding pipe.
This discharge part is connected to the water inlet of the denitrification tank 8 through a liquid supply pipe, and the liquid supply pipe connected to the water outlet of the denitrification tank is divided into two parts, one of which is processed. The other end was connected to the waste water pipe 11, which was connected to the water inlet of the nitrification tank. Denitrifying bacteria and nitrifying bacteria were attached to each other in the same manner as in Example 1. However, synthetic wastewater mainly containing ammonium carbonate was used as the wastewater, and methanol was added to the denitrification tank from the methanol supply pipe 13 at a ratio of methanol/nitrogen = 2.5. After bacterial adhesion was formed, the wastewater was treated in a denitrification tank and a nitrification tank for a residence time of 15 hours. Analysis of wastewater and treated water was conducted in the same manner as in Example 1. The processing results are shown in Table 2.
第1図、第2図は本発明を実施するための硝化
槽、脱窒槽の一具体例である。第3図、第4図は
本発明の方法を実施するための装置の具体的プロ
セス図を示す。
1…槽、2…水の流入口、3…水の流出口、4
…中空糸状膜、5…送気管、6…上部中空糸状膜
支持体、7…中空糸状膜開口端、8…脱窒槽、9
…硝化槽、10…送液ポンプ、11…廃水送液
管、12…処理水流出管、13…メタノール供給
管。
FIG. 1 and FIG. 2 are specific examples of a nitrification tank and a denitrification tank for carrying out the present invention. FIGS. 3 and 4 show specific process diagrams of an apparatus for carrying out the method of the present invention. 1...Tank, 2...Water inlet, 3...Water outlet, 4
...Hollow fiber membrane, 5...Air supply pipe, 6...Upper hollow fiber membrane support, 7...Hollow fiber membrane open end, 8...Denitrification tank, 9
...Nitrification tank, 10...Liquid sending pump, 11...Waste water sending pipe, 12...Treatment water outflow pipe, 13...Methanol supply pipe.
Claims (1)
る方法において、槽内に硝化細菌の支持体として
中空糸状膜を充填し、この内部から酸素またはこ
れを含む気体を通気するようにした硝化槽と、槽
内に脱窒細菌の支持体を充填した脱窒槽を設け、
硝化槽と脱窒槽間で水を循環することを特徴とす
る含窒素化合物を含む水の浄化方法。1. A nitrification tank in which a hollow fiber membrane is filled as a support for nitrifying bacteria and oxygen or a gas containing it is vented from inside the tank, in a method for biochemically purifying water containing nitrogen-containing compounds. Then, a denitrification tank filled with denitrifying bacteria support was installed.
A method for purifying water containing nitrogen-containing compounds, characterized by circulating water between a nitrification tank and a denitrification tank.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56010336A JPS57127493A (en) | 1981-01-27 | 1981-01-27 | Method for purification of water containing nitrogen-containing compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56010336A JPS57127493A (en) | 1981-01-27 | 1981-01-27 | Method for purification of water containing nitrogen-containing compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57127493A JPS57127493A (en) | 1982-08-07 |
| JPS6366599B2 true JPS6366599B2 (en) | 1988-12-21 |
Family
ID=11747348
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56010336A Granted JPS57127493A (en) | 1981-01-27 | 1981-01-27 | Method for purification of water containing nitrogen-containing compound |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57127493A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2565431B2 (en) * | 1991-06-20 | 1996-12-18 | 株式会社荏原製作所 | Method and apparatus for treating organic wastewater |
| JP4024330B2 (en) * | 1996-09-10 | 2007-12-19 | 水道機工株式会社 | Method and apparatus for nitrification / denitrification treatment using a single tank |
| JP2007537041A (en) * | 2004-05-14 | 2007-12-20 | ノースウエスタン ユニバーシティ | Method and system for complete nitrogen removal |
| JP5039093B2 (en) * | 2009-06-15 | 2012-10-03 | 株式会社栄電社 | Manufacturing method of bioreactor element |
-
1981
- 1981-01-27 JP JP56010336A patent/JPS57127493A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57127493A (en) | 1982-08-07 |
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