JPS6352957B2 - - Google Patents
Info
- Publication number
- JPS6352957B2 JPS6352957B2 JP8447281A JP8447281A JPS6352957B2 JP S6352957 B2 JPS6352957 B2 JP S6352957B2 JP 8447281 A JP8447281 A JP 8447281A JP 8447281 A JP8447281 A JP 8447281A JP S6352957 B2 JPS6352957 B2 JP S6352957B2
- Authority
- JP
- Japan
- Prior art keywords
- cod
- bod
- treatment
- activated carbon
- adsorption
- 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
- 238000000034 method Methods 0.000 claims description 49
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 32
- 238000001179 sorption measurement Methods 0.000 claims description 19
- 239000002351 wastewater Substances 0.000 claims description 13
- 239000002245 particle Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 4
- 229910021536 Zeolite Inorganic materials 0.000 claims description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 3
- 239000010457 zeolite Substances 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 2
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 claims description 2
- 239000003830 anthracite Substances 0.000 claims description 2
- 239000002223 garnet Substances 0.000 claims description 2
- 239000004576 sand Substances 0.000 claims description 2
- 238000004065 wastewater treatment Methods 0.000 claims 1
- 230000008569 process Effects 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 239000000126 substance Substances 0.000 description 18
- 238000005516 engineering process Methods 0.000 description 17
- 239000010802 sludge Substances 0.000 description 15
- 244000005700 microbiome Species 0.000 description 9
- 239000007788 liquid Substances 0.000 description 6
- 238000004062 sedimentation Methods 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229910052698 phosphorus Inorganic materials 0.000 description 5
- 239000011574 phosphorus Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 3
- 239000003344 environmental pollutant Substances 0.000 description 3
- 231100000719 pollutant Toxicity 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000010865 sewage Substances 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000031018 biological processes and functions Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000010800 human waste Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 230000002503 metabolic effect Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 241000790917 Dioxys <bee> Species 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000011165 process development Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 230000037351 starvation Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008719 thickening Effects 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)
Description
本発明は、都市下水、し尿のようにBOD、
COD、SSおよびNH4−Nなどを主たる汚濁因子
とする有機性排水を生物学的手段および化学的手
段によつて処理する方法に関するものである。
従来、都市下水あるいはし尿の処理技術の主流
となつているのは活性汚泥法あるいはその変法で
あり、これらの処理技術の適用によつて前記排水
中のBOD、SSは効率的に除去されるが、COD、
窒素、リンの除去は難しく、特にCODの除去機
能が不十分であつた。
そのため従来、CODなどの汚濁因子を除去す
る必要がある場合には、生物学的処理工程の後に
3次処理工程を付加するのが通常の手段となつて
いる。この3次処理工程で常用される処理技術と
しては凝集沈殿法および/または活性炭吸着法が
主体的なものであり、これらの処理技術は要求さ
れる処理水質に対応して、選択的に適用されてい
た。
これらの3次処理技術のうち、凝集沈殿法は通
常2次処理水のポリツシングを目的として適用さ
れ、前記排水中の色度成分、COD、SSの除去に
効果をあげている。この処理技術で使用される凝
集剤としては、一般的に硫酸バンド〔Al2
(SO4)2〕、塩化第2鉄〔FeCl3〕、又は消石灰〔Ca
(OH)2〕があるが、この方法の最大の利点は、
前記処理を目的とした薬注率であれば、排水中に
溶存しているリンも同時に、かつ確実に除去でき
ることであり、そのため3次処理に比較的多く適
用されている。しかしながら、凝集沈殿法には前
記利点を打消す、次のような実用上の重大な欠陥
がある。
一般的に薬注量が大であり(2次処理水への
注入Al/Pが2〜3、曝気槽への注入Al/P
が4〜5)、従つて汚泥の発生量が多い(処理
コストが高い)。
汚泥フロツクの沈降性が悪い(広大な用地面
積を必要とする)。
凝沈汚泥は一般に濃縮性が悪い(処理すべき
汚泥量が大である)。
同様に、汚泥の脱水性が悪い(汚泥処理施設
に対する負荷が大きい)。
処理プロセス内で、大量の薬品および凝沈汚
泥)を扱わざるを得ない(日常の運転管理、操
作が面倒である)。
凝沈汚泥中に濃縮されたリンの処理、処分が
全く、考慮されていない(実質的なリン除去技
術として評価しがたい)。
以上のような理由から、このような技術上の制
約を解消し、凝集沈殿法に代わりうる、すなわち
薬品を使用せず、したがつて汚泥が発生しない
か、あるいは発生してもごくわずかであり、しか
も低コストで処理ができるCOD除去技術の確立
が要望されている。
一方、活性炭吸着法は現有技術の中では、処理
しにくい汚泥を発生することなく、CODを低レ
ベルまで確実に除去できる技術として高い評価を
受けているが、この処理技術も実際処理に適用す
ることを考慮すると凝集沈殿法以上に技術上の問
題が多い。
すなわち、活性炭吸着法によるCOD除去のメ
カニズムは、例えば生物処理のようにCOD成分
を生物学的に分解除去する方法ではなく、活性炭
を単に吸着濃縮媒体として排水中のCOD成分を
活性炭表面の細孔に吸着濃縮するに過ぎない。従
つて、COD成分が活性炭の吸着飽和量に達する
とCOD成分が排水中にリークしはじめるので再
生する必要がある。活性炭の再生技術として既に
2、3の方法が確立されているが、いずれにして
も多量の薬品又は多量のエネルギーを使用せざる
を得ず、そのために再生コストが著しく高額とな
るだけでなく、再生排水を処理せざるを得ない問
題点がある。
いずれにしても活性炭吸着法は単に排水中の汚
濁原因物質を一時的に吸着濃縮するだけの処理技
術であるために、厳密にいえば処理技術として十
分評価できるものではなく、処理コストが高い欠
点もあり、実際処理に広く適用されている処理方
法とはいい難い。このように活性炭吸着法も凝集
沈殿法と同様に、この技術の改善法またはその代
替技術の開発、確立が強く要望されている。
本発明者らは、前記凝集沈殿法または活性炭吸
着法に代わりうる、簡単しかも低コストで確実に
CODが除去できる方法を模索してきたが、最近
になつて物理化学的処理技術に、最大限かつ合理
的、効率的に微生物の機能を賦与した生物物理化
学的なCOD除去技術を確立し、高度のCOD除去
機能をもつた処理プロセスを完成するに至つた。
すなわち、本発明プロセスは2段階の生物物理
化学的な処理工程より構成されており、先ず第1
段階工程によつて処理すべき排水中のBOD成分
を可及的に除去し、この段階で処理水中の
BOD/COD(BODとCODの比)を0.5以下とし、
本来的に生物分解しづらい成分が主要成分となつ
ている排水を第2段階の生物物理化学的な処理工
程に導入し、活性炭表面に吸着濃縮されたCOD
成分を好気的な条件下において生物学的に分解除
去することを特徴とする排水中のCOD除去方法
である。
本発明の技術思想の骨子は、排水中に含まれて
いる生物分解しにくいCOD成分を究極的には活
性炭および/またはその他の吸着媒体表面に濃縮
し、これらを生物の機能によつて連続的、恒久的
に再生するという概念に存在し、この原理を中核
として種々のプロセス的展開が考えられるが、以
下にその実施態様を説明する。
都市下水を活性汚泥法によつて処理したいわゆ
る2次処理水を先ず固体粒子充填層式の生物過
工程に導入する。
この工程には通常の充填層型式の過塔が使用
され、その内部に操作液面高さの1/2程度まで活
性炭、砂、アンスラサイト、ガーネツト等の過
に常用される過材が1種類又は2種類以上充填
されている。2次処理水はこの装置の上部から下
向流方向に通水され、一方、この装置の下部から
供給される空気によつて充填層内は好気的条件下
に維持される。空気の供給速度は充填された過
材の粒径に対応して、その過材が流動しない程
度に設定され、固定状態にある過材によつて
過機能が賦与される。このような装置(工程)に
2次処理水が導入され、好気的条件下で通水され
ると、2次処理水中に残留しているBOD、窒素、
リンなどの栄養物質によつて過材表面に好気性
微生物が次第に増殖し、これらの微生物の代謝活
動によつて液中のBODは可及的に分解除去され、
同時に充填された過材の生物過作用によつて
2次処理水に含まれているSSも効果的に除去さ
れる。
前記生物過工程の処理条件は生物学的に分解
され易いBODが優先的に分解されるよう考慮す
ること、つまり、この工程からの流出水の
BOD/CODが流入水に対してかなり低減される
ように設定することが大切である。この工程での
BOD除去機能が不十分で、仮に流出水のBOD/
CODがある値よりも大きいと、即ち、COD量に
対してBOD量が大きすぎると、次の流動媒体方
式の吸着工程でのCOD除去能力が著しく低下す
る。
その理由は、微生物には本来的にジオキシ作用
と称するものがあり、例えば2次処理水中に微生
物によつて資化されやすい(生物分解されやす
い)物質と資化され難い(生物分解され難い)物
質が同時に存在すると、微生物は資化されやすい
物質を優先的に分解利用し、そのため資化され難
い物質は最後まで液中に残留してしまうからであ
る。
従つて本発明の第2工程である流動媒体方式の
吸着工程にBOD/CODの大きい液が流入すると、
COD除去が期待されているにも拘らずBOD(生物
分解されやすい物質)が優先的に分解され、除去
対象であるCOD(生物分解されにくい物質)は殆
ど分解されない結果となる。
以上のように、本発明における第1工程である
生物過工程によつて処理された2次処理水の
BOD/CODはある一定値以下とすることが必要
不可欠の条件であるが、この件に関し種々研究を
重ねた結果、生物過工程からの流出水の
BOD/CODが0.5以下となるように処理すると、
第2工程である吸着工程のCOD除去機能は劣化
することなく、極めて長期間に亘つて高いCOD
除去率が維持されることが確認された。
しかして、生物過工程によつてBOD/COD
≦0.5とされた2次処理水は次いで吸着工程に導
入される。この工程の中核となつている装置は、
通常の円形槽あるいは角槽の中にエアリフト用の
ドラフトチユーブを内在させ、その下端より空気
を導入するようにしたものであり、この槽内には
流動媒体として粒状活性炭および/または吸着媒
体として汎用されるゼオライト等が槽容量の10〜
30%投入され、流入水と吸着媒体がエアリフト作
用によつて十分に循環混合される。さらにこの装
置は液体と流動媒体を分解し、液体のみを単独に
取り出す機構を備えている。
前記したように生物過工程によつてBOD/
COD≦0.5まで処理された2次処理水を吸着工程
にBOD飢餓状態下で一定期間通水すると、COD
成分を分解資化できる微生物が自然発生的に増殖
し、前記2次処理水からCODが効果的に除去さ
れる。
以上のように本発明によれば、次に示すような
工業上卓越した効果が得られ、従来除去が極めて
困難であつたCODを低コストかつ効果的に除去
することができる。
物理化学的な処理技術に微生物の代謝作用を
賦与した処理技術であるため極めて合理的であ
り、難分解性のCODだけでなく、BOD、SSな
ど他の汚濁成分も高率に除去することができ
る。
薬品を一切使用しないため処理経費が著しく
安価であり、また凝集沈殿法で発生するような
処理困難な汚泥は全く発生しない。
吸着工程用の流動媒体(活性炭、ゼオライト
など)の生物再生に要するエネルギーが、微生
物の呼吸に必要な酸素を供給するだけで補給で
きるので、従来法に比べ著しい省エネルギー化
が達成できる。
前記流動媒体は生物再生されるので、半永久
的に反復作用できる。
以下に本発明の代表的な実施例を示す。
実施例
団地下水を活性汚泥法で処理した2次処理水を
共通の供試原水として、本発明プロセスによつて
処理した実験例1および本発明の前記吸着工程の
みによつて処理した実験例2について、COD除
去能力を比較した。なお、両プロセスの性能比較
は、それぞれの工程の媒体に自然発生的に微生物
が十分に増殖し、それぞれの工程に対応した機能
が完全に認められるようになつてから(供試原水
を通水しはじめてから約3.5ケ月後)のデータを
採用して行なつた。
各実験例での処理除件を第1表に、処理成績を
第2表及び第3表に示した。なお、これらの表に
おいて第1工程は前記生物過工程を、第2工程
は前記吸着工程をそれぞれ意味している。
The present invention can be applied to urban sewage, human waste, BOD, etc.
The present invention relates to a method for treating organic wastewater containing COD, SS, NH4 -N, etc. as main pollutants by biological means and chemical means. Conventionally, the mainstream treatment technology for urban sewage or human waste has been the activated sludge method or its modified methods, and by applying these treatment technologies, BOD and SS in the wastewater can be efficiently removed. However, COD,
Removal of nitrogen and phosphorus was difficult, and the removal function of COD was particularly insufficient. Therefore, conventionally, when it is necessary to remove pollutants such as COD, it has been common practice to add a tertiary treatment step after the biological treatment step. The main treatment technologies commonly used in this tertiary treatment step are the coagulation sedimentation method and/or the activated carbon adsorption method, and these treatment technologies are selectively applied depending on the required quality of the treated water. was. Among these tertiary treatment techniques, the coagulation-sedimentation method is usually applied for the purpose of polishing the secondary treated water, and is effective in removing chromaticity components, COD, and SS from the wastewater. The flocculant used in this treatment technique is generally sulfuric acid band [Al 2
(SO 4 ) 2 ], ferric chloride [FeCl 3 ], or slaked lime [Ca
(OH) 2 ], but the biggest advantage of this method is
If the chemical injection rate is aimed at the above treatment, it is possible to simultaneously and reliably remove phosphorus dissolved in the wastewater, which is why it is relatively often applied to tertiary treatment. However, the coagulation-sedimentation method has the following serious practical drawbacks that negate the above advantages. In general, the amount of chemical injection is large (Al/P injected into the secondary treated water is 2 to 3, Al/P injected into the aeration tank).
4 to 5), therefore the amount of sludge generated is large (processing cost is high). Sludge flocs have poor settling properties (requires a large land area). Coagulated sludge generally has poor thickening properties (the amount of sludge that must be treated is large). Similarly, sludge has poor dewatering properties (large load on sludge treatment facilities). In the treatment process, large amounts of chemicals and flocculated sludge must be handled (daily operation management and operation are troublesome). The treatment and disposal of phosphorus concentrated in flocculated sludge is not considered at all (it is difficult to evaluate it as a substantial phosphorus removal technology). For the reasons mentioned above, it is possible to overcome these technical limitations and replace the coagulation-sedimentation method, i.e., it does not use chemicals and therefore generates no sludge or only generates very little sludge. There is a need to establish COD removal technology that can be treated at low cost. On the other hand, among the existing technologies, activated carbon adsorption method has received high praise as a technology that can reliably remove COD to a low level without generating sludge that is difficult to treat. Considering this, there are more technical problems than the coagulation-sedimentation method. In other words, the mechanism of COD removal using the activated carbon adsorption method is not a method that biologically decomposes and removes COD components as in biological treatment, for example, but rather uses activated carbon as an adsorption concentration medium to absorb COD components in wastewater through the pores on the surface of the activated carbon. It simply adsorbs and concentrates. Therefore, when the COD component reaches the adsorption saturation amount of the activated carbon, the COD component begins to leak into the wastewater, so it is necessary to regenerate it. A few methods have already been established as activated carbon recycling technology, but in any case, a large amount of chemicals or a large amount of energy must be used, which not only makes the recycling cost extremely high. There is a problem in that recycled wastewater must be treated. In any case, the activated carbon adsorption method is a treatment technology that simply adsorbs and concentrates pollution-causing substances in wastewater, so strictly speaking, it cannot be evaluated sufficiently as a treatment technology, and the drawback is that the treatment cost is high. Therefore, it is difficult to say that this is a processing method that is widely applied in actual processing. As described above, as with the activated carbon adsorption method, there is a strong demand for the development and establishment of improved methods of this technology or alternative technologies. The present inventors have discovered a simple, low-cost, and reliable method that can replace the coagulation-precipitation method or activated carbon adsorption method.
We have been searching for a method to remove COD, but recently we have established a biophysicochemical COD removal technology that adds microbial functions to the physicochemical treatment technology in the most rational and efficient way. We have completed a treatment process that has the ability to remove COD. That is, the process of the present invention consists of two steps of biophysical and chemical treatment steps.
BOD components in the wastewater to be treated are removed as much as possible through a stepwise process, and at this stage, the
BOD/COD (ratio of BOD and COD) should be 0.5 or less,
The wastewater, whose main components are components that are inherently difficult to biodegrade, is introduced into the second stage biophysical and chemical treatment process, and COD is adsorbed and concentrated on the activated carbon surface.
This is a method for removing COD from wastewater, which is characterized by biologically decomposing and removing components under aerobic conditions. The gist of the technical idea of the present invention is to ultimately concentrate COD components contained in wastewater that are difficult to biodegrade on the surface of activated carbon and/or other adsorption media, and to continuously release them through the functions of living organisms. exists in the concept of permanent regeneration, and various process developments can be considered based on this principle, the implementation of which will be described below. So-called secondary treated water obtained by treating municipal sewage by the activated sludge method is first introduced into a solid particle packed bed type biological filtration process. A normal packed bed type filter tower is used in this process, and one type of filter material, such as activated carbon, sand, anthracite, or garnet, is placed inside the tower up to about 1/2 of the operating liquid level. Or it is filled with two or more types. The secondary treated water is passed in a downward flow direction from the upper part of the apparatus, while the inside of the packed bed is maintained under aerobic conditions by air supplied from the lower part of the apparatus. The air supply rate is set in accordance with the particle size of the filled overfill material to such an extent that the overfill material does not flow, and the overfill material in a fixed state provides overfunction. When secondary treated water is introduced into such equipment (process) and passed under aerobic conditions, BOD, nitrogen, and
Aerobic microorganisms gradually proliferate on the surface of the overmaterial due to nutrient substances such as phosphorus, and BOD in the liquid is decomposed and removed as much as possible by the metabolic activities of these microorganisms.
At the same time, the SS contained in the secondary treated water is also effectively removed by the biological overaction of the filled overfill material. The treatment conditions for the biological process should be such that BOD, which is easily biodegradable, is preferentially degraded, that is, the effluent from this process should be
It is important to set the BOD/COD so that it is significantly reduced relative to the inflow water. In this process
If the BOD removal function is insufficient and the BOD/
When COD is larger than a certain value, that is, when the amount of BOD is too large relative to the amount of COD, the COD removal ability in the next adsorption step using the fluidized medium method is significantly reduced. The reason for this is that microorganisms inherently have a so-called dioxy effect, and for example, in secondary treated water, there are substances that are easily assimilated by microorganisms (easily biodegradable) and substances that are difficult to assimilate (hardly biodegradable). This is because when substances are present at the same time, the microorganisms preferentially decompose and utilize substances that are easily assimilated, and therefore substances that are difficult to assimilate remain in the liquid until the end. Therefore, when a liquid with a large BOD/COD flows into the fluidized medium adsorption step, which is the second step of the present invention,
Although COD removal is expected, BOD (substances that are easily biodegradable) is preferentially decomposed, and COD (substances that are difficult to biodegrade), which is the target of removal, is hardly decomposed. As mentioned above, the secondary treated water treated by the biological filtration process which is the first step in the present invention
It is essential that BOD/COD be kept below a certain value, but as a result of various studies on this issue, we have found that
When processed so that BOD/COD is 0.5 or less,
The COD removal function of the adsorption process, which is the second step, does not deteriorate and maintains high COD for an extremely long period of time.
It was confirmed that the removal rate was maintained. Therefore, BOD/COD is reduced by biological processes.
The secondary treated water determined to be ≦0.5 is then introduced into the adsorption step. The equipment that is the core of this process is
A draft tube for airlift is built into a normal circular tank or square tank, and air is introduced from the bottom end of the draft tube. The zeolite etc. to be used is 10~
30% is added, and the inflow water and adsorption medium are sufficiently circulated and mixed by air lift action. Furthermore, this device is equipped with a mechanism that separates the liquid and fluid medium and extracts only the liquid. As mentioned above, BOD/
When the secondary treated water that has been treated to COD≦0.5 is passed through the adsorption process for a certain period of time under BOD starvation conditions, COD
Microorganisms that can decompose and assimilate the components naturally proliferate, and COD is effectively removed from the secondary treated water. As described above, according to the present invention, the following industrially outstanding effects can be obtained, and COD, which has been extremely difficult to remove in the past, can be effectively removed at low cost. It is an extremely rational treatment technology that combines physicochemical treatment technology with the metabolic action of microorganisms, and is capable of removing not only persistent COD but also other pollutants such as BOD and SS at a high rate. can. Since no chemicals are used, processing costs are extremely low, and no sludge, which is difficult to process, is generated, as is the case with the coagulation-sedimentation method. The energy required for biological regeneration of the fluidized medium (activated carbon, zeolite, etc.) for the adsorption process can be replenished simply by supplying the oxygen necessary for respiration of microorganisms, resulting in significant energy savings compared to conventional methods. Since the fluid medium is bioregenerated, it can be used repeatedly on a semi-permanent basis. Representative examples of the present invention are shown below. Examples Experimental example 1 in which secondary treated water obtained by treating underground water by the activated sludge method was treated by the process of the present invention as a common test raw water, and Experimental example 2 in which it was treated only by the adsorption step of the present invention. We compared their COD removal abilities. Comparison of the performance of both processes will be conducted only after the microorganisms have naturally grown sufficiently in the medium of each process and the functions corresponding to each process have been fully recognized (by passing the sample raw water through the medium). This study was conducted using data from approximately 3.5 months after the start of the study. The treatment exclusion conditions for each experimental example are shown in Table 1, and the treatment results are shown in Tables 2 and 3. In addition, in these tables, the first step means the biological permeation step, and the second step means the adsorption step.
【表】【table】
【表】【table】
【表】
測定
第2表と第3表の比較から、本発明プロセスに
よる処理水はCODが著しく低くなつていること
がわかる。[Table] Measurement A comparison of Tables 2 and 3 shows that the COD of the water treated by the process of the present invention is significantly lower.
Claims (1)
好気的条件下において固体粒子充填層に通水して
BOD、SS、CODの部分的除去を行ないBOD/
CODを0.5以下とする第1工程と、該第1工程流
出水を好気的条件下の流動媒体方式の吸着工程に
導入して処理する第2工程から成ることを特徴と
する有機性排水のCOD除去方法。 2 前記第1工程が、前記固体粒子充填層を形成
する固体粒子として活性炭、砂、アンスラサイ
ト、ガーネツトから一種類又は2種類以上選んで
使用して処理されるものである特許請求の範囲第
1項記載の方法。 3 前記第2工程が、前記流動媒体として活性
炭、ゼオライトのいずれか少なくとも一方を使用
して処理されるものである特許請求の範囲第1項
又は第2項記載の方法。[Claims] 1. Organic wastewater containing BOD, SS and COD is passed through a solid particle packed bed under aerobic conditions.
Performs partial removal of BOD, SS, and COD.
An organic wastewater treatment method comprising a first step in which the COD is reduced to 0.5 or less, and a second step in which the effluent from the first step is introduced into an adsorption step using a fluidized medium under aerobic conditions for treatment. How to remove COD. 2. Claim 1, wherein the first step is performed using one or more selected from activated carbon, sand, anthracite, and garnet as the solid particles forming the solid particle packed bed. The method described in section. 3. The method according to claim 1 or 2, wherein the second step is performed using at least one of activated carbon and zeolite as the fluidizing medium.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8447281A JPS57201591A (en) | 1981-06-03 | 1981-06-03 | Cod eliminating method of organic waste water |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8447281A JPS57201591A (en) | 1981-06-03 | 1981-06-03 | Cod eliminating method of organic waste water |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57201591A JPS57201591A (en) | 1982-12-10 |
| JPS6352957B2 true JPS6352957B2 (en) | 1988-10-20 |
Family
ID=13831576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8447281A Granted JPS57201591A (en) | 1981-06-03 | 1981-06-03 | Cod eliminating method of organic waste water |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57201591A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02135659U (en) * | 1989-04-14 | 1990-11-13 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110563086A (en) * | 2019-09-19 | 2019-12-13 | 上海城市水资源开发利用国家工程中心有限公司 | Ecological Retention Pond Using Enhanced Phosphorus Removal Particles as Filler and Its Realization Method |
-
1981
- 1981-06-03 JP JP8447281A patent/JPS57201591A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02135659U (en) * | 1989-04-14 | 1990-11-13 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57201591A (en) | 1982-12-10 |
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