JPH01160475A - Device for immobilizing microorganism - Google Patents

Device for immobilizing microorganism

Info

Publication number
JPH01160475A
JPH01160475A JP31925187A JP31925187A JPH01160475A JP H01160475 A JPH01160475 A JP H01160475A JP 31925187 A JP31925187 A JP 31925187A JP 31925187 A JP31925187 A JP 31925187A JP H01160475 A JPH01160475 A JP H01160475A
Authority
JP
Japan
Prior art keywords
aqueous solution
microorganisms
calcium salt
polymerization catalyst
salt
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
Application number
JP31925187A
Other languages
Japanese (ja)
Other versions
JPH0528593B2 (en
Inventor
Hironori Nakamura
裕紀 中村
Tatsuo Sumino
立夫 角野
Naomichi Mori
直道 森
Ichiro Nakajima
一郎 中島
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.)
Hitachi Plant Technologies Ltd
Original Assignee
Hitachi Plant Technologies 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 Hitachi Plant Technologies Ltd filed Critical Hitachi Plant Technologies Ltd
Priority to JP31925187A priority Critical patent/JPH01160475A/en
Publication of JPH01160475A publication Critical patent/JPH01160475A/en
Publication of JPH0528593B2 publication Critical patent/JPH0528593B2/ja
Granted legal-status Critical Current

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  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)

Abstract

PURPOSE:To obtain the subject device, consisting of a dripper for a mixture solution containing microorganisms, a polymerizable chemical and water-soluble salt of alginic acid, dripper for an aqueous solution of a polymerization catalyst containing a Ca salt and further polymerization vessel and capable of providing highly active immobilized microorganisms without using a highly toxic catalyst. CONSTITUTION:An aqueous solution 7 of a polymerization catalyst prepared by mixing a calcium salt from a polymerization catalyst tank 6 is dripped through a spray nozzle 8 as fine droplets 10 into a polymerization vessel 1 containing a hydrophobic liquid 2 in the upper layer and an aqueous solution 3 of a calcium salt in the lower layer stored therein. A mixture solution 12 of microorganisms, a polymerizable chemical and a water-soluble salt of alginic acid is dripped from a mixture solution tank 11 through a nozzle 15 of a dripper 14 into a hydrophobic liquid 2 containing suspended fine droplets 10 to afford mixed droplets 17, in which the water-soluble salt of alginic acid in the interface with the aqueous solution 3 of the calcium salt is converted into an insoluble calcium salt to form a film wrapping the microorganisms and polymerizable chemical. Furthermore, the polymerizable chemical in the interior is polymerized to form immobilized microorganisms 18, which are then recovered in a storage tank 22 by a belt conveyer 21.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、種々の化学反応や廃水処理に有用な固定化微
生物を製造する微生物固定化装置に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a microorganism immobilization device for producing immobilized microorganisms useful for various chemical reactions and wastewater treatment.

〔従来技術及び発明が解決しようとする問題点〕従来、
重合性薬剤と微生物及びアルギン酸ナトリウムの混合液
を、カルシウム塩を混合した重合触媒水溶液中に滴下し
、水に不溶のアルギン酸カルシウムを生成させながら重
合性薬剤を重合させる装置が知られている。この装置で
は、簡単な操作で微生物を固定化できる。しかし、重合
触媒として一般に用いられる過硫酸塩は、微生物に対す
る毒性が強いので、微生物活性が著しく低下してしまう
[Prior art and problems to be solved by the invention] Conventionally,
An apparatus is known in which a liquid mixture of a polymerizable drug, a microorganism, and sodium alginate is dropped into an aqueous solution of a polymerization catalyst mixed with a calcium salt, and the polymerizable drug is polymerized while producing water-insoluble calcium alginate. With this device, microorganisms can be immobilized with simple operations. However, persulfates commonly used as polymerization catalysts are highly toxic to microorganisms, resulting in a significant decrease in microbial activity.

従って、強度と微生物活性が共に高い固定化微生物を得
るには、比較的高濃度の重合触媒に重合性混合液の液滴
を短時間だけ接触させ、短時間内に重合を終了させる必
要がある。     ・しかしながら、従来の装置では
、カルシウム塩含有重合触媒水溶液中に混合液の液滴が
必要以上に長時間接触され、微生物の活性が低下してし
まうという欠点があった。
Therefore, in order to obtain immobilized microorganisms with high strength and microbial activity, it is necessary to bring droplets of the polymerizable mixture into contact with a relatively highly concentrated polymerization catalyst for only a short period of time, and to complete the polymerization within a short period of time. . - However, the conventional apparatus has the disadvantage that the droplets of the mixed liquid are in contact with the calcium salt-containing polymerization catalyst aqueous solution for a longer time than necessary, resulting in a decrease in the activity of the microorganisms.

従って、本発明は、前記の従来技術の欠点を解消し、強
度及び微生物活性が共に高い固定化微生物を製造できる
微生物固定化装置を提供することを目的とする。
Therefore, an object of the present invention is to provide a microorganism immobilization device that can eliminate the drawbacks of the prior art described above and can produce immobilized microorganisms with high strength and microbial activity.

〔問題点を解決するための手段〕[Means for solving problems]

本発明は、疎水性液層中にカルシウム塩含有重合触媒水
溶液の微細な液滴を浮遊させ、そこに微生物、重合性薬
剤及びアルギン酸水溶性塩の混合液の液滴を滴下し、上
記の微細な液滴と混合液の液滴とを接触させることによ
って活性の高い固定化微生物が得られることを見出し、
前記の問題点を解決したものである。
In the present invention, fine droplets of a calcium salt-containing polymerization catalyst aqueous solution are suspended in a hydrophobic liquid layer, and droplets of a mixed solution of microorganisms, a polymerizable drug, and an alginic acid water-soluble salt are dropped therein. discovered that highly active immobilized microorganisms could be obtained by bringing liquid droplets into contact with droplets of a mixed liquid.
This solves the above problems.

すなわち、本発明の微生物固定化装置は、微生物、重合
性薬剤及びアルギン酸の水溶性塩を含む混合液の滴下装
置、カルシウム塩を混合した重合触媒水溶液の滴下装置
及び上層に疎水性液、下層にカルシウム塩水溶液を含む
重合槽から成ることを特徴とする。
That is, the microorganism immobilization device of the present invention includes a dropping device for dropping a mixed solution containing a microorganism, a polymerizable drug, and a water-soluble salt of alginic acid, a dropping device for dropping a polymerization catalyst aqueous solution mixed with a calcium salt, a hydrophobic liquid in the upper layer, and a hydrophobic liquid in the lower layer. It is characterized by consisting of a polymerization tank containing an aqueous calcium salt solution.

本発明に使用する滴下装置は、通常、ノズルを有する装
置であるが、液体の小滴を滴下しうるちのであればよい
、また、本発明の固定化装置においては、重合触媒水溶
液を重合槽の上層の疎水性液層に微細な液滴として浮遊
させておくので、重合触媒水溶液の滴下装置としては、
スプレーノズルを使用するのが好ましい。
The dropping device used in the present invention is usually a device having a nozzle, but any device capable of dropping small droplets of liquid may be used. Since it is suspended as fine droplets in the upper hydrophobic liquid layer, it can be used as a dropping device for aqueous polymerization catalyst solution.
Preferably, a spray nozzle is used.

本発明の固定化装置に使用する重合槽は、その一端から
カルシウム塩水溶液を流入させ、他端から生成固定化微
生物を排出させうる形式のものであれば、任意のもので
よい。この重合槽中で、下層を形成するカルシウム塩水
溶液は、通常、0.2〜5重量%水溶液、好ましくは0
.5〜2重量%水溶液として使用する。他方、重合槽の
上層をなす疎水性液としては、水と混和せず、比重が1
より小さく、微生物に対する毒性がほとんどない有機液
体、例えば植物油、パラフィン等を使用することができ
る。
The polymerization tank used in the immobilization apparatus of the present invention may be of any type as long as it is of a type that allows the calcium salt aqueous solution to flow in from one end and discharge the produced immobilized microorganisms from the other end. In this polymerization tank, the calcium salt aqueous solution forming the lower layer is usually a 0.2 to 5% by weight aqueous solution, preferably a 0.2 to 5% by weight aqueous solution.
.. It is used as a 5-2% by weight aqueous solution. On the other hand, the hydrophobic liquid that forms the upper layer of the polymerization tank is immiscible with water and has a specific gravity of 1.
Organic liquids that are smaller and have little toxicity to microorganisms, such as vegetable oils, paraffin, etc., can be used.

本発明の固定化装置により固定化する微生物には、特別
に制限はなく、活性汚泥、硝化菌、メタン発酵菌、シュ
ードモナス属菌、その他、生化学反応及び化学反応に関
与する各種の細菌であってよい。
The microorganisms to be immobilized by the immobilization device of the present invention are not particularly limited, and include activated sludge, nitrifying bacteria, methane-fermenting bacteria, Pseudomonas bacteria, and various other bacteria involved in biochemical and chemical reactions. It's fine.

重合性薬剤は、重合性モノマー及び溶媒、架橋剤等のモ
ノマーの重合に通常使用される物質(重合触媒を除く)
を含むものである。重合性モノマーとしては、アクリル
酸、メタクリル酸、アクリル酸エステル若しくはアクリ
ルアミド又はこれらに対応するメタクリル酸誘導体、酢
酸ビニル、ビニルアルコール等のビニルモノマーが挙ケ
ラレ、これらのモノマーの1種又は2種以上を使用する
ことができる。更に、これらの七ツマ−と共重合可能な
モノマーを重合性薬剤に包含することもできる。
Polymerizable agents include polymerizable monomers, solvents, crosslinking agents, and other substances normally used for monomer polymerization (excluding polymerization catalysts).
This includes: Examples of polymerizable monomers include acrylic acid, methacrylic acid, acrylic esters, acrylamide, or their corresponding methacrylic acid derivatives, and vinyl monomers such as vinyl acetate and vinyl alcohol. can be used. Furthermore, monomers copolymerizable with these heptamers can also be included in the polymerizable drug.

混合液には、更にアルギン酸の水溶性塩が含まれる。水
溶性塩としては、ナトリウム塩、カリウム塩、アンモニ
ウム塩等が挙げられる。アルギン酸の水溶性塩は、混合
液中に0.1〜2重量%、好ましくは0.2〜0.5重
量%の濃度で含まれる。
The liquid mixture further contains a water-soluble salt of alginic acid. Examples of water-soluble salts include sodium salts, potassium salts, ammonium salts, and the like. The water-soluble salt of alginic acid is contained in the mixed liquid at a concentration of 0.1 to 2% by weight, preferably 0.2 to 0.5% by weight.

重合触媒としては、過硫酸カリウム、過硫酸アンモニウ
ム等の過硫酸塩類、過塩素酸カリウム、過塩素酸ナトリ
ウム等の過塩素酸塩類、過酸化水素等が挙げられる。こ
れらは、0.001〜5重量%、好ましくは0.1〜1
重量%水溶液として用いられる。
Examples of the polymerization catalyst include persulfates such as potassium persulfate and ammonium persulfate, perchlorates such as potassium perchlorate and sodium perchlorate, and hydrogen peroxide. These are 0.001 to 5% by weight, preferably 0.1 to 1% by weight.
Used as a wt% aqueous solution.

重合触媒水溶液中には、混合液滴中のアルギン酸の水溶
性塩が疎水性液層内で不溶性塩を形成できるように、水
溶性のカルシウム塩を添加しておく。使用しうる水溶性
カルシウム塩としては、塩化カルシウム、臭化カルシウ
ム、硝酸カルシウム等が挙げられる。カルシウム塩は、
重合触媒水溶液中に0.2〜5重量%、好ましくは0.
5〜2重景%の濃度で添加する。
A water-soluble calcium salt is added to the polymerization catalyst aqueous solution so that the water-soluble salt of alginic acid in the mixed droplets can form an insoluble salt in the hydrophobic liquid layer. Water-soluble calcium salts that can be used include calcium chloride, calcium bromide, calcium nitrate, and the like. Calcium salt is
0.2 to 5% by weight, preferably 0.2 to 5% by weight in the polymerization catalyst aqueous solution.
Add at a concentration of 5-2%.

〔実施例〕〔Example〕

次に、図面に示した本発明の実施例に基づいて本発明を
詳述する。
Next, the present invention will be described in detail based on embodiments of the present invention shown in the drawings.

第1図は、本発明の一実施例を示す微生物固定化装置の
略示断面図である。
FIG. 1 is a schematic cross-sectional view of a microorganism immobilization device showing one embodiment of the present invention.

第1図に示した固定化装置において、重合槽1は上層に
疎水性液2、下層にカルシウム塩水溶液3を貯えている
。カルシウム塩水溶液3は水路状の重合槽1の一端に設
けた流入管4から流入し、排出管5を設けた他端に向か
って流下する。
In the immobilization apparatus shown in FIG. 1, a polymerization tank 1 stores a hydrophobic liquid 2 in the upper layer and an aqueous calcium salt solution 3 in the lower layer. The calcium salt aqueous solution 3 flows into the waterway-shaped polymerization tank 1 through an inflow pipe 4 provided at one end thereof, and flows down toward the other end provided with a discharge pipe 5.

重合槽1は、顆粒側が深くなるように底面が傾斜してい
る。また、重合を阻害する酸素を除去するため、重合槽
1の上部には、窒素ガス等の不活性ガスを導通ずるのが
好ましい。
The bottom of the polymerization tank 1 is inclined so that the granule side is deeper. Further, in order to remove oxygen that inhibits polymerization, it is preferable to conduct an inert gas such as nitrogen gas through the upper part of the polymerization tank 1.

重合触媒槽6は、カルシウム塩を混合した重合触媒水溶
液7を収容しており、スプレーノズル8は、ポンプ9で
圧送された重合触媒水溶液7を霧化して微細液滴10を
作り、該液滴を重合槽1の上流端付近の疎水性液2中に
落下させる。微細液滴10は、疎水性液層内のカルシウ
ム塩水溶液3との界面に達し、浮遊しながら流下し、界
面を満たしていく。
The polymerization catalyst tank 6 contains a polymerization catalyst aqueous solution 7 mixed with calcium salt, and the spray nozzle 8 atomizes the polymerization catalyst aqueous solution 7 pumped by a pump 9 to form fine droplets 10. is dropped into the hydrophobic liquid 2 near the upstream end of the polymerization tank 1. The fine droplets 10 reach the interface with the calcium salt aqueous solution 3 in the hydrophobic liquid layer, flow down while floating, and fill the interface.

混合液槽11は、微生物、重合性薬剤及びアルギン酸水
溶性塩の混合液12を収容しており、微生物と薬剤が均
一に混合するように攪拌機を用いて攪拌される。滴下装
置14は、比較的細いノズル15を備えており、ポンプ
16により圧送された混合液12を微細液滴10が浮遊
している疎水性液2中に滴下し、混合液滴17を作る。
The mixed liquid tank 11 contains a mixed liquid 12 of microorganisms, a polymerizable drug, and a water-soluble alginic acid salt, and is stirred using a stirrer so that the microorganisms and the drug are uniformly mixed. The dropping device 14 is equipped with a relatively narrow nozzle 15, and drops the mixed liquid 12 pumped by the pump 16 into the hydrophobic liquid 2 in which the fine droplets 10 are suspended, thereby forming mixed droplets 17.

混合液滴17の直径は、通常、1〜5鶴程度のものであ
る。
The diameter of the mixed droplet 17 is usually about 1 to 5 cranes.

混合液滴17は、疎水性液層内のカルシウム塩水溶液と
の界面に達し、ここに浮遊するカルシウム塩を混合した
重合触媒水溶液の微細液滴10と接触し、まず、アルギ
ン酸の水溶性塩が水に不溶性のカルシウム塩に変わり、
微生物及び重合性薬剤を包囲するアルギン酸カルシウム
の皮膜が形成され、更に、内部の重合性薬剤が重合固化
して混合液滴17とほぼ同じ大きさの固定化微生物18
になる。このとき、混合液滴17と微細液滴10の接触
効率を高め、また、混合液滴17同士の合体を防ぐため
、微細液滴10の直径は、固定化微生物18の粒径より
小さい、好ましくはlf1以内であることが望ましい。
The mixed droplets 17 reach the interface with the calcium salt aqueous solution in the hydrophobic liquid layer and come into contact with the fine droplets 10 of the polymerization catalyst aqueous solution mixed with the calcium salt floating there. Converts to water-insoluble calcium salts,
A film of calcium alginate surrounding the microorganisms and the polymerizable drug is formed, and the polymerizable drug inside is further polymerized and solidified to form an immobilized microorganism 18 of approximately the same size as the mixed droplet 17.
become. At this time, in order to increase the contact efficiency between the mixed droplets 17 and the fine droplets 10 and to prevent the mixed droplets 17 from coalescing, the diameter of the fine droplets 10 is preferably smaller than the particle size of the immobilized microorganisms 18. is preferably within lf1.

微細液滴10の直径は、スプレーノズル18の孔径とポ
ンプ9の圧力を変えることにより調節することができる
The diameter of the fine droplets 10 can be adjusted by changing the pore size of the spray nozzle 18 and the pressure of the pump 9.

更に、滴下された混合液滴17は、疎水性液層内のカル
シウム塩水溶液3との界面を浮遊、流下し、重合して固
定化微生物18に変わりながら、数秒から長くとも数十
秒以内に自然に下層のカルシウム塩水溶液3中に重力沈
降する。そのため、固定化微生物18が必要以上に重合
触媒水溶液7と接触するのを防ぎ、微生物の活性低下を
防止することができる。
Furthermore, the dropped mixed droplet 17 floats and flows down the interface with the calcium salt aqueous solution 3 in the hydrophobic liquid layer, polymerizes, and transforms into the immobilized microorganism 18 within a few seconds to several tens of seconds at the most. It naturally settles by gravity into the lower calcium salt aqueous solution 3. Therefore, it is possible to prevent the immobilized microorganisms 18 from coming into contact with the polymerization catalyst aqueous solution 7 more than necessary, and to prevent a decrease in the activity of the microorganisms.

界面に広がった微細液滴10も、やがてはカルシウム塩
水溶液3に溶は込み、そこの重合触媒濃度を高めていく
が、カルシウム塩水溶液槽19に収容された新鮮なカル
シウム塩水溶液3をポンプ20を用いて流入管4から供
給することにより重合触媒を微生物活性に影響しない程
度のごく低濃度に抑えることができる。
The fine droplets 10 that have spread on the interface will eventually dissolve into the calcium salt aqueous solution 3 and increase the polymerization catalyst concentration there. By supplying the polymerization catalyst from the inlet pipe 4 using a polymerization catalyst, the concentration of the polymerization catalyst can be suppressed to a very low concentration that does not affect microbial activity.

カルシウム塩水溶液3中に沈降した固定化微生物18は
、排出管5から水溶液と共に流出し、網状のベルトコン
ベア21で回収され、貯留槽22に貯留される。ベルト
コンベア21を通過したカルシウム塩水溶液3は、循環
水槽23に貯留され、一部は廃液としてオーバーフロー
し、残りはポンプ24を用いて流入管4に循環される。
The immobilized microorganisms 18 that have settled in the calcium salt aqueous solution 3 flow out from the discharge pipe 5 together with the aqueous solution, are collected by a mesh belt conveyor 21, and stored in a storage tank 22. The aqueous calcium salt solution 3 that has passed through the belt conveyor 21 is stored in a circulating water tank 23, a portion of which overflows as waste liquid, and the remainder is circulated to the inflow pipe 4 using the pump 24.

〔発明の効果〕〔Effect of the invention〕

本発明の固定化装置によれば、微生物に対して毒性の高
い重合触媒と微生物が必要以上に接触することなく、微
生物を固定化することができるので、活性の著しく高い
固定化微生物を得ることができる。
According to the immobilization device of the present invention, microorganisms can be immobilized without unnecessary contact between the microorganisms and the polymerization catalyst, which is highly toxic to microorganisms, so that immobilized microorganisms with extremely high activity can be obtained. Can be done.

本発明の固定化装置により製造される固定化微生物は、
廃水処理や微生物が関与する様々な生化学反応及び化学
反応に有効に利用される。
The immobilized microorganism produced by the immobilization device of the present invention is
It is effectively used in wastewater treatment and various biochemical and chemical reactions involving microorganisms.

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

第1図は、本発明の一実施態様を示す微生物固定化装置
の略示断面図である。 符号の説明 1・・・重合槽、2・・・疎水性液、3・・・カルシウ
ム塩水溶液、6・・・重合触媒槽、8・・・スプレーノ
ズル、11・・・混合液槽、14・・・滴下装置、15
・・・ノズル
FIG. 1 is a schematic cross-sectional view of a microorganism immobilization device showing one embodiment of the present invention. Description of symbols 1... Polymerization tank, 2... Hydrophobic liquid, 3... Calcium salt aqueous solution, 6... Polymerization catalyst tank, 8... Spray nozzle, 11... Mixed liquid tank, 14 ...Dripping device, 15
···nozzle

Claims (2)

【特許請求の範囲】[Claims] (1)微生物、重合性薬剤及びアルギン酸の水溶性塩を
含む混合液の滴下装置、カルシウム塩を混合した重合触
媒水溶液の滴下装置及び上層に疎水性液、下層にカルシ
ウム塩水溶液を含む重合槽から成ることを特徴とする微
生物固定化装置。
(1) From a dropping device for a mixed solution containing microorganisms, a polymerizable drug, and a water-soluble salt of alginic acid, a dropping device for a polymerization catalyst aqueous solution mixed with a calcium salt, and a polymerization tank containing a hydrophobic liquid in the upper layer and a calcium salt aqueous solution in the lower layer. A microorganism immobilization device characterized by:
(2)重合触媒水溶液の滴下装置を、該装置から滴下さ
れる液滴の直径が固定化微生物の粒径より小さくなるよ
うに設定した特許請求の範囲第1項記載の固定化装置。
(2) The immobilization device according to claim 1, wherein the dropping device for the aqueous polymerization catalyst solution is set so that the diameter of the droplets dropped from the device is smaller than the particle size of the immobilized microorganism.
JP31925187A 1987-12-17 1987-12-17 Device for immobilizing microorganism Granted JPH01160475A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31925187A JPH01160475A (en) 1987-12-17 1987-12-17 Device for immobilizing microorganism

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31925187A JPH01160475A (en) 1987-12-17 1987-12-17 Device for immobilizing microorganism

Publications (2)

Publication Number Publication Date
JPH01160475A true JPH01160475A (en) 1989-06-23
JPH0528593B2 JPH0528593B2 (en) 1993-04-26

Family

ID=18108105

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31925187A Granted JPH01160475A (en) 1987-12-17 1987-12-17 Device for immobilizing microorganism

Country Status (1)

Country Link
JP (1) JPH01160475A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8871249B2 (en) 2008-02-27 2014-10-28 Hisamitso Pharmaceutical Co., Inc. Medicated patch

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8871249B2 (en) 2008-02-27 2014-10-28 Hisamitso Pharmaceutical Co., Inc. Medicated patch

Also Published As

Publication number Publication date
JPH0528593B2 (en) 1993-04-26

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