JPS6254079B2 - - Google Patents
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- Publication number
- JPS6254079B2 JPS6254079B2 JP55156258A JP15625880A JPS6254079B2 JP S6254079 B2 JPS6254079 B2 JP S6254079B2 JP 55156258 A JP55156258 A JP 55156258A JP 15625880 A JP15625880 A JP 15625880A JP S6254079 B2 JPS6254079 B2 JP S6254079B2
- Authority
- JP
- Japan
- Prior art keywords
- activated carbon
- water
- treatment
- concentrated
- separated
- 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
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 99
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 67
- 238000000034 method Methods 0.000 claims description 41
- 239000010802 sludge Substances 0.000 claims description 29
- 239000000126 substance Substances 0.000 claims description 12
- 239000007800 oxidant agent Substances 0.000 claims description 9
- 239000006228 supernatant Substances 0.000 claims description 9
- 230000018044 dehydration Effects 0.000 claims description 8
- 238000006297 dehydration reaction Methods 0.000 claims description 8
- 239000002351 wastewater Substances 0.000 claims description 8
- 229910021645 metal ion Inorganic materials 0.000 claims description 7
- 238000003756 stirring Methods 0.000 claims description 6
- 239000011268 mixed slurry Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 238000010494 dissociation reaction Methods 0.000 claims description 3
- 230000005593 dissociations Effects 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 2
- 150000002505 iron Chemical class 0.000 claims 1
- 238000004065 wastewater treatment Methods 0.000 claims 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000001179 sorption measurement Methods 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000010800 human waste Substances 0.000 description 6
- 239000002002 slurry Substances 0.000 description 5
- 239000011790 ferrous sulphate Substances 0.000 description 4
- 235000003891 ferrous sulphate Nutrition 0.000 description 4
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 4
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 239000000920 calcium hydroxide Substances 0.000 description 3
- 235000011116 calcium hydroxide Nutrition 0.000 description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 3
- GPWDPLKISXZVIE-UHFFFAOYSA-N cyclo[18]carbon Chemical class C1#CC#CC#CC#CC#CC#CC#CC#CC#C1 GPWDPLKISXZVIE-UHFFFAOYSA-N 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- -1 iron ion Chemical class 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 239000005416 organic matter Substances 0.000 description 2
- 239000010865 sewage Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 101100096719 Arabidopsis thaliana SSL2 gene Proteins 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 101100366560 Panax ginseng SS10 gene Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 235000012254 magnesium hydroxide Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Landscapes
- Water Treatment By Sorption (AREA)
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
Description
【発明の詳細な説明】
本発明は廃水の高度処理方法、詳しくは、汚水
を生物学的硝化脱窒素法で処理した処理水を高度
処理する方法に関するものである。
従来、汚水の高度処理においては放流先の環境
問題から、その最終処理水中のBOD、COD、色
度、窒素およびリン等を可能な限り減少させるこ
とが求められている。
ところで、BOD成分の含有濃度が高い汚水は
まず生物処理されるが、この汚水に含有される窒
素をも除去しなければならない場合は生物学的硝
化脱窒素法によつて処理するのが通例である。汚
水として例えば、し尿を無希釈で生物学的硝化脱
窒素法で処理した場合、窒素分についてはほぼ満
足できる程度まで除去できるが、他の成分につい
ては更に高度の処理が必要である。
本発明はこのような要求にこたえ、汚水中の不
純物を効率よく除去する方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、汚水を生物学的硝化脱窒素工程
にて処理した処理水を高度処理する方法におい
て、前記生物学的硝化脱窒素工程からの流出水と
余剰汚泥との混合スラリーに酸化剤及び金属イオ
ン解離物質を添加して酸性条件下で反応させたの
ち、濃縮工程にて濃縮スラツジと濃縮分離水に分
離し、該濃縮スラツジを脱水工程で脱水して脱水
分離水と脱水ケーキに分離すると共に、前記濃縮
分離水又は、該濃縮分離水と前記脱水分離水に粉
末活性炭を添加して接続撹拌したのち、上澄水を
少なくとも粒状活性炭処理工程に導くことを特徴
とするものである。
本発明の一実施態様を図面に基づいて説明すれ
ば、し尿1はまず生物学的硝化脱窒素工程2によ
つて処理される。この脱窒素工程2の汚泥濃度を
一定濃度に調整するため、生物処理槽内の汚泥の
一部が遠心分離機3に流入し、濃縮汚泥4と分離
水5に分離され、濃縮汚泥4は脱窒素工程2へ返
送される。一方、分離水5は脱窒素工程2からの
流出スラリー6に混合される。
この流出スラリー6は従来の活性汚泥法のよう
に最終沈殿池において活性汚泥を分離した上澄水
を意味するものではなく、余剰汚泥を含有するス
ラリーを意味する。
しかして、分離水5と流出スラリー6とを混合
した混合スラリー7に過酸化水素などの酸化剤8
と金属イオン解離物質9が添加され、PH3〜4の
酸性条件下で反応槽10において所定時間撹拌さ
れる。反応槽10からの反応液は必要があれば水
酸化マグネシウム、消石灰、苛性ソーダなどの中
和剤により中和された後、濃縮槽11にて濃縮ス
ラツジ13と濃縮分離水12に分離される。
濃縮槽11により分離された濃縮分離水12に
粉末活性炭18を添加して接触槽17において所
定時間撹拌した後、必要があれば粉末活性炭処理
水19に凝集剤20を添加し、沈殿池21で粉末
活性炭を分離し、上澄水22は後続する粒状活性
炭塔25により処理され高度処理水26として系
外へ排出される。
一方、濃縮スラツジ13は脱水工程14にて脱
水分離水15と脱水ケーキ16に分離され、脱水
分離水15は必要があれば接触槽17に流入され
濃縮分離水12と共に粉末活性炭18により接触
撹拌処理され、必要がなければ沈殿池21の上澄
水22と混合され後続の処理を受ける。
なお、以下説明の便宜のため前記反応槽10に
おける化学酸化処理をフエントン処理と略称する
ことにする。
本発明は、かように反応槽10において脱窒素
工程2からの生物処理水の水の浄化と汚泥脱水の
ための汚泥の改質が同一薬品によつて同時に達成
され、従来のように汚泥脱水用の脱水助剤と凝集
沈殿用の凝集剤を各々別個に添加する必要がなく
なるという利点が得られる。
つまり、本発明は混合スラリー7に対して酸化
剤8と金属イオン解離物質9を添加してPH3〜4
に維持しながら撹拌すると、フエントン反応が起
こり、生物処理水の水の浄化と共に汚泥の改質が
行なわれることを利用するものである。
本発明においては前記金属イオン解離物質9と
しては、鉄イオン改離物質が好ましく、塩化第二
鉄、硫酸第二鉄、硫酸第一鉄、ポリ硫酸鉄のいず
れでも利用できるが、硫酸第一鉄が最も効果的で
ある。そのほかAlイオン、Cuイオンを解離する
物質も適用でき、Fe、Al、Cuのそれぞれ塩、酸
化物、水酸化物、単体金属を単独又は複数組み合
わせて使用することができる。
一方、前記酸化剤8としては過酸化水素のほか
にオゾンの使用も可能であり、これらを併用して
もよい。
濃縮液11から得られた濃縮スラツジ13は脱
水工程14により脱水されるのであるが、ここで
汚泥の脱水性を良くするには酸化剤8の量を多量
に加え汚泥を改質することが必要になるが逆に酸
化剤8の量が多いと汚泥に取り込まれていた不純
物としてのBOD、CODが溶出し後続する高度処
理工程に悪影響を及ぼす。従つて、酸化剤8の添
加量は汚泥の脱水ケーキ16の含水率をいくらに
したいかによつて決定することになるが、その量
は例えば、後記実施例に示す如く硫酸第一鉄2000
〜3000mg/、過酸化水素500〜1000mg/の場
合、脱水ケーキ16の含水率は60〜65%であり、
フエントン処理後の濃縮槽11の濃縮分離水12
の水質はBOD40〜50mg/、SS10〜30mg/、
COD50〜130mg/、色度50〜100度であつた。
かように、し尿の高度処理においてはCOD成
分を如何に経済的に減少させるかが大きなポイン
トになる。本発明において、濃縮分離水12を粉
末活性炭18と所定時間接触撹拌後、粒状活性炭
塔25で処理することにしたのは次の理由によ
る。すなわち、従来濃縮分離水に残留する汚染物
を除去するに直接粒状活性炭塔を使用していたの
であるが、本発明者らが濃縮分離水中に残留する
COD成分の処理方法について鋭意研究したとこ
ろ、濃縮分離水を直接粒状活性炭塔で処理する前
段階で前記した粉末活性炭処理することが効果的
であることが判明したからである。
すなわち、第2図に示す如く、濃縮分離水につ
いて活性炭の平衡吸着量をみると、原水濃度
(Co)がCOD100〜130mg/の場合の平衡吸着量
X/Mは約0.20g・COD/g・cとかなり高い
値を示すにも拘わらず曲線の傾きは急で、COD
を20〜30mg/まで減少させるには多量の活性炭
が必要なことがわかる。これは水中に易吸着性の
有機物と難吸着性の有機物が混合して存在してい
るためであり、第3図のCOD減少曲線(Co89
mg/)もこのことを示している。即ち、第3図
から、後記実施例に示す条件下で粉末活性炭を
200〜400mg/を添加して易吸着性の物質を除去
したのち粒状活性炭塔で処理すると、粒状活性炭
塔の寿命が大幅に伸び粉末活性炭処理コスト、粒
状活性炭処理コストの合計を、従来の直接に粒状
活性炭処理する場合のコストに比較して著しく低
減できることがわかつた。
前記粒状活性炭処理工程は前記沈殿池21の上
澄水22中に残留する汚染物を除去するためのも
のであり、ポリツシヤーとしてのこの活性炭処理
工程の吸着方式は通常の固定床式で十分であるが
活性炭塔の流入水は塔頂より供給して活性炭充填
槽を下向流で通水し処理水を塔底より抜き出し、
活性炭の移動は通水方向と逆にするいわゆる逆移
動床式吸着方式を適用すると、充填時毎に塔内を
逆洗することになるので更に動率的な吸着方式と
なる。
ところで、濃縮分離水中のCOD成分は後続の
粉末活性炭処理およびポリツシヤーとしての粒状
活性炭処理で目標とするCOD値まで減少可能で
あるが、濃縮分離水中のBOD成分の量が問題と
なるところでは後続の活性炭本来の物理的吸着作
用で除去できる量は少量であるから第1図に示す
ように上澄水22について予め生物処理工程23
で処理するとよい。なお、第1図中24は生物処
理水である。
この生物処理工程23は、通常の曝気法、生物
膜法などによる生物処理装置を使用して処理する
こともできるが、粒状活性炭処理工程を二段方式
とし、第一段目の処理では活性炭塔の塔底から連
続的に空気を導入しながら前記上澄水22を下向
流で通水して主にBOD成分を除去し二段目の処
理で通常の活性炭処理を行なうようにすることも
できる。
なお、脱水工程14からの脱水分離水15中の
COD成分の量が問題となる場合は接触槽17を
経由して処理すればよい。
以上述べたように本発明によれば合理的にかつ
効率よく廃水の高度処理を行なうことができ
BOD、COD等の低い極めて良質の高度処理水が
得られる利点がある。
次に本発明の実施例について記す。
実施例
前記実施態様の説明で引用したフローシートに
則して別表に示す性状のし尿を0.5m3/日の処理
量で無希釈処理した。各工程の処理条件は次のと
おりである。
1 生物学的硝化脱窒素工程
(1) 滞留時間
第1脱窒素槽 1日
硝 化 槽 2日
第2脱窒素槽 1日
(2) その他
水 温 27〜35℃
MLSS 15000〜20000mg/
硝化液循環比 10〜30倍
汚泥返送方法 遠心分離機使用
2 フエントン処理工程
硫酸第1鉄 2000〜3000mg/
過酸化水素 500〜1000mg/
中 和 剤 消石灰
3 濃縮工程
重力式シツクナー固形物負荷50Kg/m2・日
4 脱水工程
全自動フイルタープレス
5 粉末活性炭処理工程
粉末活性炭 200〜400mg/
滞留時間 5〜15分間
6 粒状活性炭処理工程(二段処理方式)
カラム大きさ 5.0〓cn×200L cn
流 速 SV;0.5〜1.5
活性炭量 2
まず、し尿を生物学的硝化脱窒素工程にて処理
した。次にこの生物処理工程から発生する余剰汚
泥を混合した混合スラリー(SS濃度約10000〜
12000mg/)に硫酸第1鉄2000〜3000mg/と
過酸化水素500〜1000mg/を添加しPH3〜4の
条件下で3〜5時間撹拌したのち、消石灰でPH
5.5に中和し、さらに重力式シツクナーで固液分
離し、18000〜20000mg/の濃縮スラツジと濃縮
分離水を得た。この濃縮スラツジを全自動フイル
タープレスで脱水した結果、含水率60〜65%の脱
水ケーキが得られた。
一方、濃縮分離水に粉末活性炭200〜400mg/
を添加し、5〜15分間接触撹拌した後沈殿池に導
き、アニオンポリマー3〜5mg/を添加して粉
末活性炭およびSSを沈降させた後、粒状活性炭
塔の流入水とした。第一段粒状活性炭塔には塔底
から少量の空気を連続的に導入すると共に沈殿池
上澄水を下向流に通水し、処理水中にDOが2
mg/以上残留するように維持した。その後通常
の活性炭塔へ下向流に通水した。(第1図、第2
図及び第3図参照)
かくて得られた濃縮分離水、粉末活性炭処理水
及び最終処理水としての粒状活性炭処理水の性
状、水質は下表のとおりである。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for advanced treatment of wastewater, and more particularly, to a method for advanced treatment of treated water obtained by treating wastewater by biological nitrification and denitrification. Conventionally, in advanced treatment of wastewater, it has been required to reduce BOD, COD, chromaticity, nitrogen, phosphorus, etc. in the final treated water as much as possible due to environmental problems at the destination. By the way, sewage with a high concentration of BOD components is first subjected to biological treatment, but if the nitrogen contained in this sewage must also be removed, it is customary to treat it using biological nitrification and denitrification methods. be. For example, when human waste is treated as wastewater without dilution using the biological nitrification and denitrification method, the nitrogen content can be removed to a nearly satisfactory level, but other components require more advanced treatment. The present invention meets these demands and aims to provide a method for efficiently removing impurities from wastewater. That is, the present invention provides a method for advanced treatment of treated water obtained by treating wastewater in a biological nitrification and denitrification process, in which an oxidizing agent and After adding a metal ion dissociation substance and reacting under acidic conditions, it is separated into concentrated sludge and concentrated separated water in a concentration step, and the concentrated sludge is dehydrated in a dehydration step to be separated into dehydrated separated water and dehydrated cake. In addition, after adding powdered activated carbon to the concentrated separated water or the concentrated separated water and the dehydrated separated water and stirring them together, the supernatant water is led to at least a granular activated carbon treatment step. If one embodiment of the present invention is described based on the drawings, human waste 1 is first treated in a biological nitrification and denitrification process 2. In order to adjust the sludge concentration in this denitrification process 2 to a constant concentration, a part of the sludge in the biological treatment tank flows into the centrifuge 3 and is separated into thickened sludge 4 and separated water 5, and the thickened sludge 4 is denitrified. Returned to nitrogen process 2. Meanwhile, the separated water 5 is mixed into the effluent slurry 6 from the denitrification step 2. This effluent slurry 6 does not mean supernatant water from which activated sludge has been separated in a final settling tank as in the conventional activated sludge method, but rather a slurry containing excess sludge. Thus, an oxidizing agent 8 such as hydrogen peroxide is added to the mixed slurry 7 which is a mixture of the separated water 5 and the effluent slurry 6.
and metal ion dissociation substance 9 are added, and stirred for a predetermined time in a reaction tank 10 under acidic conditions of pH 3 to 4. The reaction liquid from the reaction tank 10 is neutralized with a neutralizing agent such as magnesium hydroxide, slaked lime, or caustic soda, if necessary, and then separated into a concentrated sludge 13 and concentrated separated water 12 in a concentration tank 11. Powdered activated carbon 18 is added to the concentrated separated water 12 separated by the concentration tank 11 and stirred for a predetermined time in the contact tank 17. If necessary, a flocculant 20 is added to the powdered activated carbon treated water 19, and the mixture is stirred in the settling tank 21. The powdered activated carbon is separated, and the supernatant water 22 is treated in the subsequent granular activated carbon tower 25 and discharged to the outside of the system as highly treated water 26. On the other hand, the concentrated sludge 13 is separated into dehydrated separated water 15 and dehydrated cake 16 in the dehydration step 14, and the dehydrated separated water 15 is flowed into a contact tank 17 if necessary, and is subjected to contact stirring treatment with the concentrated separated water 12 using powdered activated carbon 18. If it is not necessary, it is mixed with the supernatant water 22 of the sedimentation tank 21 and subjected to subsequent treatment. Note that, for convenience of explanation, the chemical oxidation treatment in the reaction tank 10 will be abbreviated as Fenton treatment below. In this way, in the reaction tank 10, the purification of the biologically treated water from the denitrification process 2 and the reforming of sludge for sludge dewatering are simultaneously achieved using the same chemical, and the sludge dewatering process is completed as before. There is an advantage that there is no need to separately add a dehydration aid for use and a flocculant for coagulation and precipitation. That is, the present invention adds an oxidizing agent 8 and a metal ion dissociative substance 9 to the mixed slurry 7 to achieve a pH of 3 to 4.
This method takes advantage of the fact that when stirred while maintaining a constant temperature, the Fuenton reaction occurs, which purifies the biologically treated water and reforms the sludge. In the present invention, the metal ion dissociating substance 9 is preferably an iron ion dissociating substance, and any of ferric chloride, ferric sulfate, ferrous sulfate, and polyferrous sulfate can be used, but ferrous sulfate is the most effective. In addition, substances that dissociate Al ions and Cu ions can also be used, and salts, oxides, hydroxides, and single metals of Fe, Al, and Cu can be used alone or in combination. On the other hand, as the oxidizing agent 8, ozone can be used in addition to hydrogen peroxide, and these may be used in combination. The concentrated sludge 13 obtained from the concentrated liquid 11 is dehydrated in a dehydration step 14, but in order to improve the dewatering properties of the sludge, it is necessary to add a large amount of oxidizing agent 8 to reform the sludge. On the other hand, if the amount of oxidizing agent 8 is large, BOD and COD as impurities incorporated in the sludge will be eluted and have a negative impact on the subsequent advanced treatment process. Therefore, the amount of the oxidizing agent 8 to be added is determined depending on the desired moisture content of the dehydrated sludge cake 16.
~3000mg/, hydrogen peroxide 500~1000mg/, the moisture content of the dehydrated cake 16 is 60~65%,
Concentrated separated water 12 in concentration tank 11 after Fuenton treatment
The water quality is BOD40~50mg/, SS10~30mg/,
COD was 50 to 130 mg/, and chromaticity was 50 to 100 degrees. Thus, in advanced treatment of human waste, a key point is how to economically reduce COD components. In the present invention, the reason why it was decided to treat concentrated separated water 12 in granular activated carbon column 25 after contacting and stirring powdered activated carbon 18 for a predetermined period of time is as follows. That is, conventionally, a granular activated carbon column was directly used to remove the contaminants remaining in the concentrated separated water, but the present inventors
This is because, after intensive research into methods for treating COD components, it was found that it is effective to perform the powdered activated carbon treatment described above before directly treating the concentrated separated water in the granular activated carbon tower. That is, as shown in Figure 2, when looking at the equilibrium adsorption amount of activated carbon for concentrated separated water, when the raw water concentration (Co) is COD 100 to 130 mg/, the equilibrium adsorption amount X/M is approximately 0.20 g・COD/g・Although the value of c is quite high, the slope of the curve is steep, and COD
It can be seen that a large amount of activated carbon is required to reduce the amount of carbon to 20-30mg/. This is due to the presence of a mixture of easily adsorbable organic matter and poorly adsorbable organic matter in water, and the COD reduction curve (Co89
mg/) also shows this. That is, from FIG. 3, powdered activated carbon was prepared under the conditions shown in Examples below.
By adding 200 to 400 mg of easily adsorbable substances and then treating it in a granular activated carbon tower, the life of the granular activated carbon tower is greatly extended, and the total cost of powdered activated carbon processing and granular activated carbon processing cost can be reduced compared to the conventional direct treatment cost. It was found that the cost can be significantly reduced compared to the case of granular activated carbon treatment. The granular activated carbon treatment step is for removing contaminants remaining in the supernatant water 22 of the sedimentation tank 21, and as for the adsorption method of this activated carbon treatment step as a polisher, a normal fixed bed type is sufficient. The inflow water of the activated carbon tower is supplied from the top of the tower, passed through the activated carbon packed tank in a downward flow, and the treated water is extracted from the bottom of the tower.
If a so-called reverse moving bed adsorption system is applied in which activated carbon is moved in the opposite direction to the water flow direction, the interior of the column will be backwashed every time it is filled, resulting in a more dynamic adsorption system. By the way, the COD component in concentrated separated water can be reduced to the target COD value by subsequent powdered activated carbon treatment and granular activated carbon treatment as a polisher, but where the amount of BOD components in concentrated separated water is a problem, the subsequent Since the amount that can be removed by the physical adsorption effect of activated carbon is small, as shown in FIG.
It is best to process it with In addition, 24 in FIG. 1 is biologically treated water. This biological treatment step 23 can be carried out using a biological treatment device using a normal aeration method, biofilm method, etc., but the granular activated carbon treatment step is a two-stage method, and the first stage treatment is performed using an activated carbon tower. It is also possible to pass the supernatant water 22 in a downward flow while continuously introducing air from the bottom of the tower to mainly remove BOD components, and perform normal activated carbon treatment in the second stage of treatment. . In addition, in the dehydrated separated water 15 from the dehydration step 14,
If the amount of COD components is a problem, it may be treated via the contact tank 17. As described above, according to the present invention, advanced treatment of wastewater can be carried out rationally and efficiently.
This method has the advantage of providing extremely high quality highly treated water with low BOD, COD, etc. Next, examples of the present invention will be described. Example In accordance with the flow sheet cited in the description of the embodiment, human waste having the properties shown in the attached table was treated without dilution at a treatment rate of 0.5 m 3 /day. The processing conditions for each step are as follows. 1 Biological nitrification and denitrification process (1) Residence time 1st denitrification tank 1 day Nitrification tank 2 days 2nd denitrification tank 1 day (2) Other water temperature 27-35℃ MLSS 15000-20000mg/Nitrification liquid circulation Sludge return method: 10 to 30 times Centrifugal separator 2 Fuenton treatment process Ferrous sulfate 2000 to 3000 mg/ Hydrogen peroxide 500 to 1000 mg/ Neutralizing agent Slaked lime 3 Concentration process Gravity thickener Solid load 50 Kg/m 2 days 4 Dehydration process Fully automatic filter press 5 Powdered activated carbon treatment process Powdered activated carbon 200-400mg/residence time 5-15 minutes 6 Granular activated carbon treatment process (two-stage treatment method) Column size 5.0〓 cn × 200 L cn flow rate SV; 0.5 ~1.5 Activated carbon amount 2 First, human waste was treated in a biological nitrification and denitrification process. Next, a mixed slurry (SS concentration of approximately 10,000 ~
Add 2000-3000mg/of ferrous sulfate and 500-1000mg/hydrogen peroxide to 12000mg/), stir for 3-5 hours under PH3-4 conditions, and then adjust the pH with slaked lime.
5.5, and then solid-liquid separation was performed using a gravity thickener to obtain concentrated sludge and concentrated separated water of 18,000 to 20,000 mg/ml. This concentrated sludge was dehydrated using a fully automatic filter press, resulting in a dehydrated cake with a water content of 60-65%. On the other hand, 200 to 400 mg of powdered activated carbon/
After contact stirring for 5 to 15 minutes, the mixture was introduced into a settling basin, and 3 to 5 mg of anionic polymer was added thereto to precipitate the powdered activated carbon and SS, which was then used as the inflow water of the granular activated carbon tower. A small amount of air is continuously introduced into the first stage granular activated carbon tower from the bottom of the tower, and the supernatant clear water of the settling tank is passed in a downward direction.
The concentration was maintained at a level of 1 mg/mg or more. Thereafter, the water was passed in a downward flow to a conventional activated carbon tower. (Fig. 1, 2
(See Figures and Figure 3) The properties and quality of the concentrated separated water, powdered activated carbon treated water, and granular activated carbon treated water as the final treated water are as shown in the table below. 【table】
第1図は本発明の一実施態様を示す系統説明
図、第2図は活性炭の平衡吸着量を示す線図、第
3図は粉末活性炭についてのCOD減少曲線であ
る。
1…し尿、2…脱窒素工程、3…遠心分離機、
4…濃縮汚泥、5…分離水、6…流出スラリー、
7…混合スラリー、8…酸化剤、9…金属イオン
解離物質、10…反応槽、11…濃縮液、12…
濃縮分離水、13…濃縮スラツジ、14…脱水工
程、15…脱水分離水、16…脱水ケーキ、17
…接触槽、18…粉末活性炭、19…粉末活性炭
処理水、20…凝集剤、21…沈殿池、22…上
澄水、23…生物処理工程、24…生物処理水、
25…粒状活性炭槽、26…高度処理水。
FIG. 1 is a system explanatory diagram showing one embodiment of the present invention, FIG. 2 is a diagram showing the equilibrium adsorption amount of activated carbon, and FIG. 3 is a COD reduction curve for powdered activated carbon. 1... human waste, 2... denitrification process, 3... centrifugal separator,
4...Thickened sludge, 5...Separated water, 6...Outflow slurry,
7... Mixed slurry, 8... Oxidizing agent, 9... Metal ion dissociated substance, 10... Reaction tank, 11... Concentrate, 12...
Concentrated separated water, 13... Concentrated sludge, 14... Dehydration step, 15... Dehydrated separated water, 16... Dehydrated cake, 17
... Contact tank, 18 ... Powdered activated carbon, 19 ... Powdered activated carbon treated water, 20 ... Coagulant, 21 ... Sedimentation tank, 22 ... Supernatant water, 23 ... Biological treatment process, 24 ... Biological treatment water,
25... Granular activated carbon tank, 26... Highly treated water.
Claims (1)
処理水を高度処理する方法において、前記生物学
的硝化脱窒素工程の処理水と余剰汚泥との混合ス
ラリーに酸化剤と金属イオン解離物質を添加し酸
性条件下で反応させたのち、濃縮工程にて濃縮ス
ラツジと濃縮分離水に分離し、前記濃縮スラツジ
を脱水工程で脱水して脱水分離水と脱水ケーキに
分離すると共に、前記濃縮分離水又は該濃縮分離
水と前記脱水分離水に粉末活性炭を添加して接触
撹拌したのち固液分離し、得られる上澄水を粒状
活性炭処理工程を含む後処理工程に導くことを特
徴とする汚水の高度処理方法。 2 前記後処理工程が、前段としての生物処理工
程と後段としての前記粒状活性炭処理工程からな
るものである特許請求の範囲第1項記載の方法。 3 前記粉末活性炭処理後の前記生物処理工程
が、粒状活性炭充填層に空気を導入して処理され
るものである特許請求の範囲第2項記載の方法。 4 前記金属イオン解離物質として鉄塩を使用す
る特許請求の範囲第1項、第2項又は第3項記載
の方法。[Scope of Claims] 1. A method for advanced treatment of treated water obtained by treating wastewater in a biological nitrification and denitrification process, wherein an oxidizing agent is added to a mixed slurry of the treated water from the biological nitrification and denitrification process and excess sludge. After adding a metal ion dissociated substance and reacting under acidic conditions, the concentrated sludge is separated into concentrated sludge and concentrated separated water in a concentration step, and the concentrated sludge is dehydrated in a dehydration step to be separated into dehydrated separated water and dehydrated cake. At the same time, powdered activated carbon is added to the concentrated separated water or the concentrated separated water and the dehydrated separated water, and after contact stirring, solid-liquid separation is carried out, and the resulting supernatant water is led to a post-treatment process including a granular activated carbon treatment process. Features: Advanced wastewater treatment method. 2. The method according to claim 1, wherein the post-treatment step comprises a biological treatment step as a first stage and the granular activated carbon treatment step as a second stage. 3. The method according to claim 2, wherein the biological treatment step after the powdered activated carbon treatment is performed by introducing air into a bed filled with granular activated carbon. 4. The method according to claim 1, 2 or 3, wherein an iron salt is used as the metal ion dissociation substance.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55156258A JPS5781890A (en) | 1980-11-06 | 1980-11-06 | High degree treatment of sewage |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55156258A JPS5781890A (en) | 1980-11-06 | 1980-11-06 | High degree treatment of sewage |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5781890A JPS5781890A (en) | 1982-05-22 |
| JPS6254079B2 true JPS6254079B2 (en) | 1987-11-13 |
Family
ID=15623859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55156258A Granted JPS5781890A (en) | 1980-11-06 | 1980-11-06 | High degree treatment of sewage |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5781890A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102838201A (en) * | 2012-09-28 | 2012-12-26 | 天津莱特化工有限公司 | Process for treating industrial wastewater by enhanced Fenton method |
-
1980
- 1980-11-06 JP JP55156258A patent/JPS5781890A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5781890A (en) | 1982-05-22 |
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