JPS61157391A - Removal of ss and phosphorus in sewage - Google Patents
Removal of ss and phosphorus in sewageInfo
- Publication number
- JPS61157391A JPS61157391A JP27432784A JP27432784A JPS61157391A JP S61157391 A JPS61157391 A JP S61157391A JP 27432784 A JP27432784 A JP 27432784A JP 27432784 A JP27432784 A JP 27432784A JP S61157391 A JPS61157391 A JP S61157391A
- Authority
- JP
- Japan
- Prior art keywords
- pipe
- phosphorus
- filter material
- acid
- sewage
- 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.)
- Granted
Links
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims abstract description 20
- 239000011574 phosphorus Substances 0.000 title claims abstract description 20
- 229910052698 phosphorus Inorganic materials 0.000 title claims abstract description 20
- 239000010865 sewage Substances 0.000 title abstract description 12
- 239000000463 material Substances 0.000 claims abstract description 41
- 238000012546 transfer Methods 0.000 claims abstract description 25
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 23
- 239000003513 alkali Substances 0.000 claims abstract description 15
- 239000002253 acid Substances 0.000 claims abstract description 13
- 239000011575 calcium Substances 0.000 claims abstract description 10
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 10
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 9
- 238000007664 blowing Methods 0.000 claims abstract description 6
- 238000000034 method Methods 0.000 claims description 22
- 239000002351 wastewater Substances 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 35
- 238000006243 chemical reaction Methods 0.000 abstract description 10
- 230000001172 regenerating effect Effects 0.000 abstract description 2
- 230000008929 regeneration Effects 0.000 description 9
- 238000011069 regeneration method Methods 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000002367 phosphate rock Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 235000011116 calcium hydroxide Nutrition 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000006114 decarboxylation reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000012851 eutrophication Methods 0.000 description 1
- 210000002816 gill Anatomy 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010800 human waste Substances 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000009287 sand filtration Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Removal Of Specific Substances (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、下水、し尿処理水或いは工場廃水等の汚水中
に含まれるSS及びリンを除去する方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for removing SS and phosphorus contained in wastewater such as sewage, human waste water, or industrial wastewater.
近年、閉鎖水域の富栄養化の進行に伴ない、これら水域
に流入する汚水中のSS及びリンを除去する方法に関す
る研究が各所で行われている。In recent years, with the progress of eutrophication of closed water bodies, research on methods for removing SS and phosphorus from wastewater flowing into these water bodies has been conducted in various places.
リン金倉む汚水をリン鉱石や骨炭などのf材(脱リン剤
ンと接触させて処理する方法は、接触説リン法として当
業者間においてによく知られており、この方法は汚泥の
発生がないので有望な方法として期待されている。The method of treating sewage by bringing it into contact with a dephosphorizing agent such as phosphate rock or bone charcoal is well known among those skilled in the art as the contact phosphorus method, and this method reduces the generation of sludge. Therefore, it is expected to be a promising method.
しかしながら、この方法においては長期間通水を継続し
ていると、脱リン材(濾材)が0aOO3や有機物によ
り汚染され、しばしば処理水質が悪化して来ることがあ
った。このような欠点を除くため、汚水を脱炭酸工程に
導き、汚水から炭酸物質を除去し友後カルシウム剤及び
/又はアルカリ剤を添加し、ついで砂濾過槽に通液して
汚水中の8Eli除去した後さらに脱リン材を充填した
脱リン槽へ通液する方法がとられていた。しかし、この
方法は工程が複雑となるばかりでなく、脱炭酸に要する
多量の酸が必要であるという欠点ヲ有している。However, in this method, if water continues to flow for a long period of time, the dephosphorization material (filter material) becomes contaminated with OaOO3 and organic matter, and the quality of the treated water often deteriorates. In order to eliminate these drawbacks, wastewater is introduced into a decarbonation process to remove carbonic substances from the wastewater, add a calcium agent and/or an alkaline agent, and then pass through a sand filtration tank to remove 8Eli from the wastewater. After that, the solution was passed through a dephosphorization tank filled with dephosphorization material. However, this method has the disadvantage that not only the process is complicated, but also a large amount of acid is required for decarboxylation.
一方、汚水中のssy除去する方法として、を材の一部
を常時循環再生しながら処理する移動床1過方法も公知
であるが、この方法でti 17ンの除去ができず、ま
たSSに汚染された濾材の再生を十分に行い難く、シた
がって濾材の移送が部分的にできなくなり目詰りを生ず
る欠点もあった。On the other hand, as a method for removing ssy from wastewater, a moving bed 1 filtration method is known in which a part of the ssy material is constantly circulated and regenerated, but this method cannot remove ti 17 There is also the disadvantage that it is difficult to sufficiently regenerate contaminated filter media, and therefore, the transport of the filter media becomes partially impossible, resulting in clogging.
本発明は、汚水にカルシウム剤及び/又はアルカリ剤を
加え皮後リン除去能力を有する濾材と接触せしめて汚水
中の8S及びリンを除去する方法において、f材層の下
部エフ1材の一部を抜き出し、この抜き出したr材に酸
又はアルカリt−加えて再生しりゝ濾材層の上部に移送
することt%徴とする汚水中の8S及びリンを除去する
方法であって、本発明者は前記の従来の技術の問題点全
解決する次め検討を重ねた結果なされ友もので、接触脱
リン法と移動床濾過法t?有機的に結合し、液中のSS
及びリンを効率的に除去する方法に関するものである。The present invention provides a method for removing 8S and phosphorus from wastewater by adding a calcium agent and/or an alkaline agent to the wastewater and bringing it into contact with a filter medium having a postcutaneous phosphorus removal ability. The present inventor has proposed a method for removing 8S and phosphorus from wastewater, which comprises extracting 8S and phosphorus from sewage, adding acid or alkali to the extracted material, and transferring the recycled material to the upper part of the filter layer. As a result of repeated studies to solve all the problems of the above-mentioned conventional techniques, the catalytic dephosphorization method and the moving bed filtration method were developed. Organically bound SS in liquid
and a method for efficiently removing phosphorus.
つぎに本発明の実施態様を第1図に基いて説明する。Next, an embodiment of the present invention will be explained based on FIG.
第1図において、符号1は汚水導入管、2にカルシウム
剤及び/又はアルカリ剤導入管、3は管内混合器、4は
反応槽、5は分配量、6は脱リン材層、7は空気吹込管
、8はrR<又はアルカリ】導入管、9は移送管、10
は空気逃し筒、11は再生槽、12ij分配傘、13は
洗浄水排出管、14は処理水排出管、15は洗浄水ぜき
t示す。In Fig. 1, numeral 1 is a wastewater introduction pipe, 2 is a calcium agent and/or alkali agent introduction pipe, 3 is an in-pipe mixer, 4 is a reaction tank, 5 is a distribution amount, 6 is a dephosphorization material layer, and 7 is air. Blowing pipe, 8 is rR<or alkali] introduction pipe, 9 is transfer pipe, 10
11 is a regeneration tank, 12 is a distribution umbrella, 13 is a washing water discharge pipe, 14 is a treated water discharge pipe, and 15 is a washing water jet.
汚水導入管1全通して供給される汚水中に、カルシウム
剤及び/又はアルカリ剤導入管2エクカルシクム剤及び
/又はアルカリ剤全注入し、管内混合器5中で混合した
抜脱リン材全充填した反応槽4に導入する。反応槽に導
入された汚 ず1水は、分配量5で分配され脱リン
材層を上向きに流れリンが除去され次後処理水排出管1
5から排出される。一方、移送管9の下部に空気を吹き
込むことにエフ脱リン材の一部は移送管内を上向きに移
送される。また移送管の下部に重文導入管8エク酸を注
入することに、、cす酸は空気にエフ混合される。そし
て、反応槽4の下部から移送管9中に導入され几脱リン
材上に付着している汚染物質は空気の攪拌作用に19剥
離されるとともに、汚染物質として付着している炭酸カ
ルシウムは酸にニジ溶解され、生成した炭酸分は空気に
エフ脱気されながら移送管中を再生されつ\ある脱リン
濾材とともに上向きに移送される。上向きに移送され九
脱すンr材は、上部再生槽11中に排出され、該再生槽
中で、再生槽の下部エフ流入する処理水により洗浄され
、処理水と向流で分配量12上で分配されながら脱リン
材層上に返送される。再生槽中で分離され几空気及び脱
気され几ガス成分は空気逃し筒10エリ系外に排出され
、ま友洗浄水は洗浄水ぜき15t−通V洗浄水排出管1
3ニジ排出される。一方処理水は処理水排出管14↓り
系外に排出される。Calcium agent and/or alkali agent inlet tube 2 Ecalcicum agent and/or alkali agent were completely injected into the wastewater supplied through sewage inlet tube 1, and the dephosphorization material mixed in pipe mixer 5 was completely filled. Introduced into reaction tank 4. The dirt 1 water introduced into the reaction tank is distributed at a distribution rate 5, flows upward through the dephosphorization material layer to remove phosphorus, and then passes through the post-treated water discharge pipe 1.
It is discharged from 5. On the other hand, by blowing air into the lower part of the transfer pipe 9, a part of the E-dephosphorization material is transferred upward in the transfer pipe. In addition, by injecting 8 ecuic acid into the lower part of the transfer tube, the citric acid is mixed with the air. The contaminants that are introduced into the transfer pipe 9 from the lower part of the reaction tank 4 and adhered to the dephosphorizing material are peeled off by the agitation action of the air, and the calcium carbonate that has adhered as a contaminant is removed by the acidic acid. The generated carbonic acid is degassed by air and transported upward through the transfer pipe together with the dephosphorizing filter medium that is being regenerated. The decomposed material transferred upward is discharged into the upper regeneration tank 11, where it is washed by treated water flowing into the lower part of the regeneration tank, and is distributed over the distribution volume 12 in countercurrent to the treated water. While being distributed, it is returned onto the dephosphorization material layer. The cooled air and degassed air are separated in the regeneration tank and the cooled gas components are discharged to the outside of the air relief pipe 10.
3 times are discharged. On the other hand, the treated water is discharged to the outside of the system through the treated water discharge pipe 14.
第2図は、脱リン材を反応槽外に設は次移送管にエリ移
送しながら再生する装置の例を示すもので、符号は第1
図に関し記載し次符号と同じ意味を有する。なお、第2
図に示す例においては、脱リンr材から分離された空気
等は、再生槽11の上部から系外に排出されるものであ
る。Figure 2 shows an example of a device in which dephosphorization material is placed outside the reaction tank and regenerated while being transferred to the next transfer pipe.
Descriptions related to figures have the same meaning as the following symbols. In addition, the second
In the example shown in the figure, air and the like separated from the dephosphorized r material are discharged from the upper part of the regeneration tank 11 to the outside of the system.
つぎに$5図に基いて本発明の他の実施の態様を説明す
る。第3図において、第1図と同じ符号は同じ意味を有
し、符号16はr材移送ポンプ、17は圧力水管、18
は攪拌機、19はアルカリ又は有機溶媒導入管金示す。Next, other embodiments of the present invention will be described based on the $5 figure. In FIG. 3, the same symbols as in FIG. 1 have the same meanings, 16 is the r material transfer pump, 17 is the pressure water pipe,
19 indicates a stirrer, and 19 indicates a tube for introducing an alkali or organic solvent.
第5図に示す装置においては、反応槽4の外部に設けた
移送管9により脱リン材の一部全移送して再生するもの
であるが、脱リン材の移送を移送ポンプ16によって行
うものである。第3図に示す例においては、下部濾材の
移送をスムースに行うため、r材吸込部に処理水の一部
を流入させるための圧力水管17に設けである。In the apparatus shown in FIG. 5, part of the dephosphorizing material is transferred and regenerated by a transfer pipe 9 provided outside the reaction tank 4, but the dephosphorizing material is transferred by a transfer pump 16. It is. In the example shown in FIG. 3, in order to smoothly transfer the lower filter medium, it is provided in the pressure water pipe 17 for causing a part of the treated water to flow into the r-material suction section.
ま友、脱リン材の再生及び洗浄を効率良く行りために再
生槽11に攪拌機18を設けている。In order to efficiently regenerate and clean the dephosphorizing material, a stirrer 18 is provided in the regeneration tank 11.
また脱リン材の有機汚染がひどい場合には、酸導入管8
エク有機rRt−注入しても工いが、このエラな場合、
アルカリ又は有機溶媒全注入するためその導入管19t
−移送管9上に設けている。In addition, if the dephosphorization material has severe organic contamination, the acid inlet pipe 8
Even if you inject organic rRt, it will not work, but if this error occurs,
19t inlet pipe for injecting all alkali or organic solvent
- on the transfer tube 9;
脱リン材としてハ、リン鉱石、骨炭、軽炉スラグ、軽焼
マグネシア等を使用でき、濾材(脱リン材2の粒径とし
てはα5I+I11〜2−0wm811のものが好まし
い。As the dephosphorizing material, phosphate rock, bone charcoal, light furnace slag, light burnt magnesia, etc. can be used, and the particle size of the filtering material (dephosphorizing material 2 is preferably α5I+I11 to 2-0wm811).
流入汚水に混合するカルシウム剤としては、石膏、塩化
カルシウム及び/又は消石灰を、アルカリ剤としは消石
石灰、苛性ソーダ及び/又は水散化マグネシウムを使用
できる。Gypsum, calcium chloride and/or slaked lime can be used as the calcium agent to be mixed with the inflowing sewage, and slaked lime, caustic soda and/or aqueous magnesium can be used as the alkaline agent.
脱リン剤が炭酸カルシウムにエラ、主として汚染されて
いる場合には、再生剤として#1酸、硫酸、有機酸等の
酸を用いるのが好ましく、また有機物により汚染されて
いる場合には、再生剤として有機酸、アルカリ或いは有
機溶媒を使用するのが好ましい。If the dephosphorizing agent is mainly contaminated with calcium carbonate, it is preferable to use an acid such as #1 acid, sulfuric acid, or an organic acid as a regenerating agent. Preferably, organic acids, alkalis or organic solvents are used as agents.
移送管9の下部に吹き込む空気は、移送管の高さにもよ
るが、a 5 % 2 kg7cm”程度の加圧空気を
、処理水量の1lL1〜5倍程度の量で吹き込めげよく
、再生塔11への洗浄用処理水量は、全処理水量の5〜
15%程度の量となるようにすればLい。The air blown into the lower part of the transfer pipe 9 depends on the height of the transfer pipe, but about 5% 2 kg 7 cm of pressurized air is blown into the lower part of the transfer pipe 9 in an amount of about 1 to 5 times the amount of 1 liter of treated water, and the regeneration tower is The amount of treated water for washing to 11 is 5 to 5 of the total amount of treated water.
If the amount is about 15%, it will be L.
移送管中に注入する酸の量は、移送管内の液がpH5〜
6になる程度、アルカリの量は移送管内のpHが10〜
12になる程度の量で加えるとよい。The amount of acid injected into the transfer tube is determined when the liquid in the transfer tube has a pH of 5 to
The amount of alkali is such that the pH in the transfer tube is 10 to 6.
It is best to add in an amount of about 12.
実施例1
塔高2500m、内径380mの第1図に示す如き装置
に、(L5〜18mのリン鉱石?:800鱈の厚さに充
填し、pHa5〜?、o、Ca含有素60〜80 mW
/ lに調整した下水二次処理水t−120m3/日
の割合で通水した。Example 1 A device as shown in Fig. 1 having a column height of 2500 m and an inner diameter of 380 m was filled with (L5 to 18 m of phosphate rock to a thickness of 800 mW), pH of 5 to ?, o, and Ca-containing elements of 60 to 80 mW.
Water was passed through at a rate of t-120 m3/day of secondary treated sewage water adjusted to /l.
槽内に19■φのエアリフト管金設け、空気全1.5j
/分(揚砂86111!/、時)の割合で吹 +
1き込んだ。また同時にエアリフト管内に1%の塩酸を
注入し、エアリフト管の上部に設けた再生塔(容量1t
)内のpHが4.5になるエラにし友。A 19 φ air lift pipe is installed in the tank, total air 1.5J
Blowing at a rate of /min (lifting sand 86111!/, hours) +
I put in 1. At the same time, 1% hydrochloric acid was injected into the air lift pipe, and a regeneration tower (capacity 1 t) was installed at the top of the air lift pipe.
) has a pH of 4.5.
処理結果′9r堀−iに示す。なお、比較例として塩酸
の注入を行わなかつ几場合の結果も表−1に示す。The processing results are shown in '9r Hori-i. As a comparative example, Table 1 also shows the results obtained without injection of hydrochloric acid.
なお、下水二次処理水の水質は、リン含有量1〜2 m
W/L SM−アルカリ度100 mW / AsS
B 5〜7 mf/l、 pH& 5〜7.0であった
。In addition, the water quality of the secondary sewage treatment water has a phosphorus content of 1 to 2 m
W/L SM-alkalinity 100 mW/AsS
B 5-7 mf/l, pH & 5-7.0.
表 −1
表−1に示されるように、本発明方法によれば長期間に
わ建って処理水のリン濃度を安定して低レベルに維持−
できるが、比較例においては処理水の水質が徐々に悪化
した。また、比較例においては6か月経過した時点から
脱リン材層の一部が固まり、濾過抵抗の上昇がみられ友
。Table 1 As shown in Table 1, the method of the present invention maintains the phosphorus concentration of treated water at a stable low level for a long period of time.
However, in the comparative example, the quality of the treated water gradually deteriorated. In addition, in the comparative example, a portion of the dephosphorization material layer solidified after 6 months, and an increase in filtration resistance was observed.
実施例2
実施例1で用いたのと同じ装置を用いて有機性排水の処
理を行った。エアリフト管内には1゜チのNaOHt−
注入し、pHが10〜11になる工うに添加量を調節し
た。一方、比較例としてNaOH1r:注入しないで試
験を行っ九。Example 2 The same equipment used in Example 1 was used to treat organic wastewater. Inside the air lift tube, there is 1° of NaOHt-
The amount added was adjusted until the pH reached 10-11. On the other hand, as a comparative example, a test was conducted without injecting NaOH1r.
結果全表−2に示す。The complete results are shown in Table-2.
表 −2
原水水質ニリン5〜4mf74M−アルカリ度50mf
/1s g 1o mW/l、 色度 50’pa6
.5〜7.0
衆−2に示すように、本発明方法においてな長期間安定
して処理水の水質を維持でき九が、比較例においては処
理水中のリン濃度が次第に高くなつt6また、比較例に
おいては5か刃稜から濾材が茶色に変色し、かつ、6か
刃稜エラ脱すン層の1部に目詰りを生じ濾過抵抗が上昇
した。Table-2 Raw water quality Nilin 5-4mf74M-Alkalinity 50mf
/1s g 1o mW/l, chromaticity 50'pa6
.. 5-7.0 As shown in Figure 2, the method of the present invention can maintain the quality of treated water stably for a long period of time, but in the comparative example, the phosphorus concentration in the treated water gradually increases. In example 5, the filter medium turned brown from the edge of the blade, and part of the layer where the gills of the edge of the blade were removed became clogged, resulting in an increase in filtration resistance.
本発明によれば、常時脱リン材を再生できるので、脱リ
ン材の汚染がなく、従って一つの反応槽で長期間安定し
て効率的にSS及びリン全除去することができる。According to the present invention, since the dephosphorization material can be constantly regenerated, there is no contamination of the dephosphorization material, and therefore, SS and phosphorus can be completely removed stably and efficiently for a long period of time in one reaction tank.
第1図、第2図及び第3図は、本発明方法全説明するた
めの概略フロー図を示す。
1・・汚水導入管、2・・カルシウム剤及び/又はアル
カリ剤導入管、3・・管内混合器、4・・反応槽、5・
・分配傘、6・・脱リン材層、7・・空気吹込管、8・
・酸又はアルカリ導入管、9・・移送管、10・・空気
逃し筒、11・・再生槽、12・・分配傘、13・・洗
浄水排出管、14・・処理水排出管、15゛。
洗浄水ぜき、16・・f材移送ポンプ、17・・圧力水
管、18・・攪拌機、19・・アルカリ又は有機溶媒導
入管1, 2 and 3 show schematic flow diagrams for explaining the entire method of the invention. 1. Sewage introduction pipe, 2. Calcium agent and/or alkali agent introduction pipe, 3. In-pipe mixer, 4. Reaction tank, 5.
・Distribution umbrella, 6.・Dephosphorization material layer, 7.・Air blowing pipe, 8.
・Acid or alkali introduction pipe, 9. Transfer pipe, 10. Air relief tube, 11. Regeneration tank, 12. Distribution umbrella, 13. Washing water discharge pipe, 14. Treated water discharge pipe, 15゛. . Washing water spout, 16...F material transfer pump, 17...pressure water pipe, 18...stirrer, 19...alkali or organic solvent introduction pipe
Claims (1)
後リン除去能力を有する濾材と接触せしめて汚水中のS
S及びリンを除去する方法において、濾材層の下部より
濾材の一部を抜き出し、この抜き出した濾材に酸又はア
ルカリを加えて再生しつゝ濾材層の上部に移送すること
を特徴とする汚水中のSS及びリンを除去する方法。 2、移送管中に空気を吹き込むことにより抜き出した濾
材を移送する特許請求の範囲第1項記載の汚水中のSS
及びリンを除去する方法。[Claims] 1. After adding a calcium agent and/or an alkaline agent to wastewater, the S in the wastewater is removed by contacting it with a filter medium having phosphorus removal ability.
A method for removing S and phosphorus from waste water, which is characterized by extracting a part of the filter material from the lower part of the filter material layer, adding acid or alkali to the extracted filter material to regenerate it, and transferring it to the upper part of the filter material layer. A method for removing SS and phosphorus. 2. SS in wastewater according to claim 1, which transfers the filter material extracted by blowing air into the transfer pipe.
and a method for removing phosphorus.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27432784A JPS61157391A (en) | 1984-12-28 | 1984-12-28 | Removal of ss and phosphorus in sewage |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27432784A JPS61157391A (en) | 1984-12-28 | 1984-12-28 | Removal of ss and phosphorus in sewage |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61157391A true JPS61157391A (en) | 1986-07-17 |
JPH0128628B2 JPH0128628B2 (en) | 1989-06-05 |
Family
ID=17540108
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27432784A Granted JPS61157391A (en) | 1984-12-28 | 1984-12-28 | Removal of ss and phosphorus in sewage |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61157391A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002307078A (en) * | 2001-04-17 | 2002-10-22 | Kurita Water Ind Ltd | Crystallization dephosphorization equipment |
JP2005305279A (en) * | 2004-04-20 | 2005-11-04 | Miyama Kk | Method and apparatus for treating fluorine-containing water |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS607992A (en) * | 1983-06-29 | 1985-01-16 | Kurita Water Ind Ltd | Fluidized bed type dephosphorization apparatus |
-
1984
- 1984-12-28 JP JP27432784A patent/JPS61157391A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS607992A (en) * | 1983-06-29 | 1985-01-16 | Kurita Water Ind Ltd | Fluidized bed type dephosphorization apparatus |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002307078A (en) * | 2001-04-17 | 2002-10-22 | Kurita Water Ind Ltd | Crystallization dephosphorization equipment |
JP2005305279A (en) * | 2004-04-20 | 2005-11-04 | Miyama Kk | Method and apparatus for treating fluorine-containing water |
JP4628013B2 (en) * | 2004-04-20 | 2011-02-09 | ミヤマ株式会社 | Fluorine-containing water treatment apparatus and treatment method |
Also Published As
Publication number | Publication date |
---|---|
JPH0128628B2 (en) | 1989-06-05 |
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