JPH0137983B2 - - Google Patents

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Publication number
JPH0137983B2
JPH0137983B2 JP5559785A JP5559785A JPH0137983B2 JP H0137983 B2 JPH0137983 B2 JP H0137983B2 JP 5559785 A JP5559785 A JP 5559785A JP 5559785 A JP5559785 A JP 5559785A JP H0137983 B2 JPH0137983 B2 JP H0137983B2
Authority
JP
Japan
Prior art keywords
phosphorus
wastewater
water
solid particles
calcium
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
Application number
JP5559785A
Other languages
Japanese (ja)
Other versions
JPS61216795A (en
Inventor
Izumi Hirasawa
Nobuyuki Iwai
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ebara Corp
Original Assignee
Ebara Infilco Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ebara Infilco Co Ltd filed Critical Ebara Infilco Co Ltd
Priority to JP5559785A priority Critical patent/JPS61216795A/en
Publication of JPS61216795A publication Critical patent/JPS61216795A/en
Publication of JPH0137983B2 publication Critical patent/JPH0137983B2/ja
Granted legal-status Critical Current

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  • Removal Of Specific Substances (AREA)
  • Water Treatment By Sorption (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

「産業上の利用分野」 本発明は、下水、し尿あるいは工場排水中に含
まれるリン及びSSを除去する方法に関する。 「従来技術」 リンを含む排水を流動化させたリン酸塩鉱物
(リン鉱石)とカルシウム、アルカリの存在下で
接触させ、排水中のリンをアパタイトCa10
(OH)2(PO46の形で、該鉱物濾材上に晶析させ
る方法は公知の技術であり、処理しにくい汚泥の
発生量が少ない点で有効な方法として期待されて
いる。 「発明が解決しようとする問題点」 従来の方法は、排水中に含まれるリンの大部分
を、濾材上に固定できるものの、濾材が流動化状
態で相互に衝突するため、濾材上の反応物の一部
が剥離したり、液中で生成された微細なアパタイ
トや排水中のSSが処理水に流出し、後段に砂濾
過を設けた場合、濾材層が短期間で目詰りを起し
逆洗頻度が高くなつたり、逆洗によつて排出され
る固形物の処理も厄介であつた。本発明はこれら
の点を解決せんとするものである。 「問題点を解決するための手段」 本発明は、リン含有廃水をカルシウム、アルカ
リの存在下でリン除去能力を有する固体粒子と接
触せしめる流動層式脱リン方法において、該廃水
をアニオンポリマーの存在下で、該固体粒子と接
触させることを特徴とするリン含有廃水の処理方
法であつて、本発明者は前記の従来の技術の問題
点を解決するため検討を重ねた結果なされたもの
で、濾材の流動化した反応槽において、反応液と
濾材をアニオンポリマーの存在下で接触させるこ
とにより、排水中に存在するリン及びSSを効率
的に除去する方法に関するものである。本願発明
の実施態様の工程の流れを第1図を用いて説明す
る。 カルシウム塩2または、アルカリ剤3を添加し
た、リンを含有する排水(原水)1と、反応槽9
の流出水の一部に、さらにカルシウム塩5または
アルカリ剤6を添加した循環水4とを混合せし
め、反応槽9に通水する。ここで反応槽にアニオ
ンポリマー7を注入し、アニオンポリマーの存在
下で流動化したリン除去能力を有する固体粒子8
と接触させることにより、排水中のリンとSSの
一部が除去される。反応槽流出水の一部は循環水
4、残りは、砂などの濾材11を充填した濾過槽
12へ通液し、主としてSS性のリンや残りのSS
を除去する。 カルシウム塩としては、塩化カルシウム、石
膏、消石灰、アルカリ剤としては、消石灰、苛性
ソーダが使用できる。 カルシウム剤及びアルカリ剤の注入方法として
は、原水にカルシウム剤を注入し、アルカリ剤を
循環水に注入する方法、原水にアルカリ剤を注入
し、循環水にカルシウム剤を注入する方法、原水
にカルシウム剤及びアルカリ剤を注入し、かつ循
環水中に反応に不足なカルシウム剤やアルカリ剤
を注入する方法、さらに、循環水にカルシウム剤
とアルカリ剤を注入する方法がある。 アルカリ剤の注入は、反応槽内の液のPHを検知
しながら注入することが望ましい。 原水と循環水の混合比は、1:1〜1:3が好
ましい。反応槽に注入するアニオンポリマーは、
ポリアクリル酸ナトリウム、ポリアクリルアミ
ド、マレイン酸共重合物などが良く、注入量は
0.2〜1mg/が良好である。 アニオンポリマーの注入位置は、反応槽内が良
い。 反応槽内の通液速度は、リン除去能力を有する
固体粒子が流動化するために必要な速度とし、該
固体粒子の粒径や密度によつて定める。なお、固
体粒子とは、リン鉱石、骨炭、鹿沼土、軽焼マグ
ネシアなど、リン除去能力を有するものである。 以上のように本願においては、流動層式脱リン
方法において、Ca2+、OH-を調整した液をアニ
オンポリマーの存在下で、リン除去能力を有す
る、濾材と接触させることにより、濾材相互の相
互の衝突や反応の過程生成するSSを濾材上に固
定できるため流動層式脱リン法のリン除去率(リ
ン固定率)を著しく向上できるとともに、後段の
濾過工程の逆洗頻度を少なくできるか、濾過工程
を省略できる。 実施例 1 内径100mmφ、有効深さ2.5mの円筒状で、底部
が逆円錘形をした脱リン塔に破砕、篩分けしたリ
ン鉱石(直効径0.4mm、均等係数1.4)を1000mm厚
に充填した。 工場排水を活性汚泥処理した2次処理水を原水
とし、これにCaSO4・2H2Oを200mg/(Caと
して50mg/)添加し、消石灰を添加した循環水
(原水流量の2倍量)と混合せしめ、脱リン塔に
流入させる。消石灰の注入は、処理水のPHが9.5
になるようにした。 反応槽内の通液速度は、リン鉱石が流動化する
30m/hとした。さらに反応槽下部に、アニオン
ポリマーを0.5mg/注入し、リン鉱石と接触さ
せた。 脱リン槽流出水の一部は、内径200mm〓に、アン
スラサイト(有効径0.8mm、均等係数1.5)を800
mm厚に充填し、LV200m/日で通水した。通水2
ケ月間の平均値を表−1に、また比較例としてア
ニオンポリマーを入れない場合、原水に直接注入
した場合を示す。
"Industrial Application Field" The present invention relates to a method for removing phosphorus and SS contained in sewage, human waste, or industrial wastewater. "Prior art" Wastewater containing phosphorus is brought into contact with fluidized phosphate mineral (phosphate rock) in the presence of calcium and alkali, and the phosphorus in the wastewater is converted to apatite Ca 10
The method of crystallizing (OH) 2 (PO 4 ) 6 on the mineral filter medium is a known technique and is expected to be an effective method since it generates a small amount of sludge that is difficult to treat. ``Problems to be Solved by the Invention'' In the conventional method, most of the phosphorus contained in wastewater can be fixed on the filter medium, but since the filter mediums collide with each other in a fluidized state, reactants on the filter medium are If a part of the filter material peels off, or if fine apatite generated in the liquid or SS in the wastewater leaks into the treated water, and if a sand filtration is installed in the latter stage, the filter layer will become clogged in a short period of time and the problem will be reversed. The frequency of washing increased, and the disposal of solids discharged by backwashing was also troublesome. The present invention aims to solve these problems. "Means for Solving the Problems" The present invention provides a fluidized bed dephosphorization method in which phosphorus-containing wastewater is brought into contact with solid particles having phosphorus removal ability in the presence of calcium and alkali. Below is a method for treating phosphorus-containing wastewater characterized by bringing it into contact with the solid particles, which was developed as a result of the inventor's repeated studies to solve the problems of the conventional technology described above. The present invention relates to a method for efficiently removing phosphorus and SS present in wastewater by contacting a reaction solution with a filter medium in the presence of an anionic polymer in a reaction tank in which the filter medium is fluidized. The process flow of an embodiment of the present invention will be explained using FIG. 1. Phosphorus-containing wastewater (raw water) 1 to which calcium salt 2 or alkali agent 3 has been added, and reaction tank 9
Part of the effluent water is mixed with circulating water 4 to which calcium salt 5 or alkali agent 6 has been added, and the water is passed into reaction tank 9. Here, the anionic polymer 7 is injected into the reaction tank, and the solid particles 8 having phosphorus removal ability are fluidized in the presence of the anionic polymer.
By contacting with water, some of the phosphorus and SS in the wastewater are removed. A part of the reaction tank outflow water is circulated water 4, and the rest is passed through a filter tank 12 filled with a filter medium 11 such as sand, which mainly removes SS phosphorus and remaining SS.
remove. Calcium chloride, gypsum, and slaked lime can be used as calcium salts, and slaked lime and caustic soda can be used as alkaline agents. Methods for injecting calcium and alkaline agents include: injecting a calcium agent into raw water and then injecting the alkaline agent into circulating water; injecting an alkaline agent into raw water and then injecting a calcium agent into circulating water; There is a method in which calcium and alkaline agents are injected into the circulating water, and calcium and alkaline agents insufficient for the reaction are injected into the circulating water, and there is a method in which a calcium agent and an alkaline agent are injected into the circulating water. It is desirable to inject the alkaline agent while detecting the pH of the liquid in the reaction tank. The mixing ratio of raw water and circulating water is preferably 1:1 to 1:3. The anionic polymer injected into the reaction tank is
Sodium polyacrylate, polyacrylamide, maleic acid copolymer, etc. are good, and the injection amount is
0.2 to 1 mg/is good. The anionic polymer is preferably injected into the reaction tank. The flow rate of the liquid in the reaction tank is the rate necessary for fluidizing the solid particles having phosphorus removal ability, and is determined by the particle size and density of the solid particles. Note that the solid particles are those having phosphorus removal ability, such as phosphate rock, bone charcoal, Kanuma soil, and lightly burnt magnesia. As described above, in the present application, in the fluidized bed dephosphorization method, a solution in which Ca 2+ and OH - have been adjusted is brought into contact with a filter medium having phosphorus removal ability in the presence of an anionic polymer, thereby increasing the mutual interaction between the filter media. Since SS generated during mutual collisions and reactions can be fixed on the filter medium, the phosphorus removal rate (phosphorus fixation rate) of fluidized bed dephosphorization can be significantly improved, and the frequency of backwashing in the subsequent filtration process can be reduced. , the filtration step can be omitted. Example 1 Crushed and sieved phosphate rock (direct diameter 0.4 mm, uniformity factor 1.4) was placed in a 1000 mm thick dephosphorization tower with an inner diameter of 100 mm and an effective depth of 2.5 m, with an inverted conical bottom. Filled. Secondary treated water obtained by treating factory wastewater with activated sludge is used as raw water, and 200 mg/(50 mg/as Ca) of CaSO 4 2H 2 O is added to it, and circulating water (twice the flow rate of raw water) is added with slaked lime. Mix and flow into the dephosphorization tower. Injection of slaked lime reduces the pH of the treated water to 9.5.
I made it so that The liquid flow rate in the reaction tank is such that the phosphate rock becomes fluidized.
The speed was 30m/h. Further, 0.5 mg of anionic polymer was injected into the lower part of the reaction tank and brought into contact with phosphate rock. A part of the water flowing out of the dephosphorization tank was filled with 800 ml of anthracite (effective diameter 0.8 mm, uniformity factor 1.5) with an inner diameter of 200 mm.
It was filled to a thickness of mm and water was passed through at a LV of 200 m/day. Water passage 2
Table 1 shows the average values for 3 months, and also shows the cases where anionic polymer was not added and where it was directly injected into raw water as a comparative example.

【表】 実施例 2 実施例1において、アニオンポリマーの注入量
を変化さ、脱リン塔流出水のSS及びリン濃度の
変化を測定した。
[Table] Example 2 In Example 1, the amount of anionic polymer injected was changed and the changes in SS and phosphorus concentration of the dephosphorization tower effluent were measured.

【表】 アニオンポリマーの注入率は0.2mg/以上で
良好であつたが、1mg/以上では反応槽の下部
で濾材相互が合一し、均一な流動層が形成され
ず、水質が悪化した。 「発明の効果」 以上のように本願の発明によつて、流動層式脱
リン方法において、Ca2+、OH-を調整した液を
アニオンポリマーの存在下で、リン除去能力を有
する、濾材と接触させることにより、濾材相互の
衝突や反応の過程生成する微細なSSを濾材上に
固定できるため、流動層式脱リン方法のリン除去
率(リン固定率)を著しく向上できるとともに、
後段の濾過工程の逆洗頻度を少なくできるか、濾
過工程を省略できる。また除去されたリンは、濾
材上にリン酸カルシウムの形で確実に固定される
ので、いわゆるフロツク状の処理しにくい汚泥は
排出されず汚泥発生量が低減できる。
[Table] The injection rate of the anionic polymer was good at 0.2 mg/or more, but at 1 mg/or more, the filter media coalesced together at the bottom of the reaction tank, a uniform fluidized bed was not formed, and the water quality deteriorated. "Effects of the Invention" As described above, according to the present invention, in a fluidized bed dephosphorization method, a solution in which Ca 2+ and OH - have been adjusted can be mixed with a filter medium having phosphorus removal ability in the presence of an anionic polymer. By bringing them into contact, fine SS generated during collisions and reactions between the filter media can be fixed onto the filter media, which can significantly improve the phosphorus removal rate (phosphorus fixation rate) of the fluidized bed dephosphorization method.
The frequency of backwashing in the subsequent filtration process can be reduced, or the filtration process can be omitted. Furthermore, since the removed phosphorus is reliably fixed in the form of calcium phosphate on the filter medium, so-called floc-like sludge that is difficult to treat is not discharged, and the amount of sludge generated can be reduced.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の一実施態様の工程の流れを示
す説明図である。 1……排水(原水)、2,5……カルシウム塩、
3,6……アルカリ剤、4……循環水、7……ア
ニオンポリマー、8……リン除去能力を有する固
体粒子、9……反応槽(流動層)、10……流動
層の処理水、11……濾過材、12……濾過槽、
13……処理水。
FIG. 1 is an explanatory diagram showing the process flow of one embodiment of the present invention. 1...Drainage (raw water), 2,5...Calcium salt,
3, 6... Alkaline agent, 4... Circulating water, 7... Anionic polymer, 8... Solid particles having phosphorus removal ability, 9... Reaction tank (fluidized bed), 10... Fluidized bed treated water, 11...filter material, 12...filter tank,
13... Treated water.

Claims (1)

【特許請求の範囲】 1 リン含有廃水をカルシウム、アルカリの存在
下で、リン除去能力を有する固体粒子と接触せし
める流動層式脱リン方式において、該廃水をアニ
オンポリマーの存在下で前記固体粒子と接触せし
めることを特徴とするリン含有廃水の処理方法。 2 リン除去能力を有する固体粒子が、リン鉱
石、骨炭、鹿沼土、軽焼マグネシアより選ばれる
特許請求の範囲第1項記載のリン含有廃水の処理
方法。
[Claims] 1. In a fluidized bed dephosphorization method in which phosphorus-containing wastewater is brought into contact with solid particles having phosphorus removal ability in the presence of calcium and alkali, the wastewater is brought into contact with the solid particles in the presence of an anionic polymer. A method for treating phosphorus-containing wastewater characterized by contacting the wastewater. 2. The method for treating phosphorus-containing wastewater according to claim 1, wherein the solid particles having phosphorus removal ability are selected from phosphate rock, bone charcoal, Kanuma soil, and light burnt magnesia.
JP5559785A 1985-03-19 1985-03-19 Treatment of phosphorus-containing waste water Granted JPS61216795A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5559785A JPS61216795A (en) 1985-03-19 1985-03-19 Treatment of phosphorus-containing waste water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5559785A JPS61216795A (en) 1985-03-19 1985-03-19 Treatment of phosphorus-containing waste water

Publications (2)

Publication Number Publication Date
JPS61216795A JPS61216795A (en) 1986-09-26
JPH0137983B2 true JPH0137983B2 (en) 1989-08-10

Family

ID=13003178

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5559785A Granted JPS61216795A (en) 1985-03-19 1985-03-19 Treatment of phosphorus-containing waste water

Country Status (1)

Country Link
JP (1) JPS61216795A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUT75444A (en) * 1992-06-23 1997-05-28 Water Board Process for the remoual of phosphorous
JP4519965B2 (en) * 1999-08-10 2010-08-04 三菱化工機株式会社 Crystallization dephosphorization apparatus and crystallization dephosphorization method
JP4519485B2 (en) * 2004-03-04 2010-08-04 荏原エンジニアリングサービス株式会社 Phosphorus recovery method and apparatus
JP5540034B2 (en) * 2012-03-07 2014-07-02 三井造船環境エンジニアリング株式会社 Phosphorus recovery equipment for phosphorus-containing water
JP2016047534A (en) * 2015-11-12 2016-04-07 三井造船環境エンジニアリング株式会社 Phosphorus recovery equipment for phosphorus-containing water

Also Published As

Publication number Publication date
JPS61216795A (en) 1986-09-26

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