JPS6156087A - Production of organic acid by immobilized microorganism - Google Patents

Production of organic acid by immobilized microorganism

Info

Publication number
JPS6156087A
JPS6156087A JP59177167A JP17716784A JPS6156087A JP S6156087 A JPS6156087 A JP S6156087A JP 59177167 A JP59177167 A JP 59177167A JP 17716784 A JP17716784 A JP 17716784A JP S6156087 A JPS6156087 A JP S6156087A
Authority
JP
Japan
Prior art keywords
immobilized
temperature
acid
waste water
carried out
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
JP59177167A
Other languages
Japanese (ja)
Other versions
JPS6324678B2 (en
Inventor
Shigeru Morimura
茂 森村
Makio Kishimoto
岸本 眞希男
Kenji Kida
建次 木田
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 Zosen Corp
Original Assignee
Hitachi Zosen Corp
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 Zosen Corp filed Critical Hitachi Zosen Corp
Priority to JP59177167A priority Critical patent/JPS6156087A/en
Publication of JPS6156087A publication Critical patent/JPS6156087A/en
Publication of JPS6324678B2 publication Critical patent/JPS6324678B2/ja
Granted legal-status Critical Current

Links

Classifications

    • Y02W10/12

Landscapes

  • Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

PURPOSE:To produce and recover a useful organic acid, in high efficiency, by treating waste water containing organic materials with immobilized microorganisms capable of producing the acid. CONSTITUTION:Microorganisms capable of producing an organic acid are included in a gelatinous carrier, and immobilized by conventional immobilization technique. The immobilized microorganisms are proliferated by cultivation, and made to contact with waste water containing organic materials. The cultivation and the contact of the immobilized microorganism with the organic-containing waste water is carried out at 20-45 deg.C and 4-6pH in the case of using a medium- temperature digestion sludge of sewage as the seed sludge, or at 45-60 deg.C and 4-6pH in the case of using a high-temperature digestion sludge. For example, the immobilized microorganisms and waste water are charged to a fermentation tank composed of the jacket 1, the fluidizing zone 2, and the settling zone 3, and the fermentation of the waste water is carried out. The fluidizing zone 2 is furnished with the device 4 to control and display the temperature and pH. The generated gas is separated by the gas-separator 5 and discharged from the reactor.

Description

【発明の詳細な説明】 産業上の利用分野 この発明は、酸生成能を有する固定化微生物によって有
機物含有廃水を処理して有機酸を生成する方法に関する
ものである。ずなわら、この発明は、有機物含有廃水を
単に処理するだけでなく、有機酸という有用な物質を生
成し、必要であればこれを回収することのできる方法に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application This invention relates to a method for producing organic acids by treating organic substance-containing wastewater using immobilized microorganisms capable of producing acids. The present invention, of course, relates to a method that not only treats organic matter-containing wastewater, but also produces useful substances called organic acids, which can be recovered if necessary.

従来技術J′3よびその問題点 従来、有礪物含有廃水の処理は、活性汚泥法などの好気
的処理による方法や、一般的メタン発酵法によりなされ
て来た。
Prior Art J'3 and its Problems Conventionally, wastewater containing solids has been treated by an aerobic treatment method such as an activated sludge method, or by a general methane fermentation method.

しかし前者の場合には、曝気槽内の溶存酸素を1〜4m
 g/I存在せしめる必要があり、BoOが高くなるほ
ど大きな曝気動力を必要とし、また生成される汚泥虫も
0.5〜0.7o  (MLSS)/a  (BOD)
と多く、余剰汚泥の処分にも苦慮した。他方後者の場合
には、メタン生成菌の増殖速度が遅く、また廃水の槽内
滞留日数を短縮すると有機酸が蓄積し、これが直接的に
またはpH1を下げることから間接的にメタン生成菌の
増殖を阻害することになるため、10日〜30日もの滞
留日数が必要となった。したがってこの方法もエネルギ
ー生産プロセスとしては現実的なものでなく、その改善
がe:!!まれていた。
However, in the former case, the dissolved oxygen in the aeration tank should be
The higher the BoO, the greater the aeration power required, and the sludge insects generated are also 0.5 to 0.7o (MLSS)/a (BOD).
There were many problems, and it was difficult to dispose of the excess sludge. On the other hand, in the latter case, the growth rate of methane-producing bacteria is slow, and if the residence time of wastewater in the tank is shortened, organic acids accumulate, which directly or indirectly reduces the pH 1, thereby increasing the growth of methane-producing bacteria. This resulted in the need for a retention period of 10 to 30 days. Therefore, this method is also not realistic as an energy production process, and its improvement is e:! ! It was rare.

またこれらの方法はいずれも廃水処理ないしメタン生成
を主目的とするものであり、発酵によって生じる有用な
有機酸を積極的に生成せしめることを企図したものでは
なかった。
In addition, all of these methods are primarily aimed at wastewater treatment or methane production, and are not designed to actively produce useful organic acids produced by fermentation.

この発明は、このような実情から上記諸問題をことごと
く解決して、有は物含有廃水の処理により有用な有機酸
を偵(本釣に生成することのできる方法を提供すること
を目的とする。
The purpose of this invention is to solve all of the above-mentioned problems under these circumstances and to provide a method that can produce useful organic acids by treating wastewater containing substances. .

問題点を解決するための手段 この発明は、担体に固定化した酸生成能を有する微生物
を培養して増殖させ、ついで固定化微生物を有機物含有
完本と接触させることを特徴とする固定化微生物による
酸生成方法である。
Means for Solving the Problems This invention provides an immobilized microorganism characterized by culturing and proliferating a microorganism having acid-producing ability immobilized on a carrier, and then bringing the immobilized microorganism into contact with an organic matter-containing whole. This is an acid production method.

種汚泥として下水処理場の中温消化汚泥を用いる場合に
1よ、固定化微生物の培養および固定化微生物と有礪物
含有廃水との接触を温度20〜45℃好ましくは35〜
40°C,11H4,0〜6.0好ましくは5.0〜5
.5の条件下に行なう。
When medium-temperature digested sludge from a sewage treatment plant is used as the seed sludge, culture of the immobilized microorganisms and contact of the immobilized microorganisms with the wastewater containing fertilized substances are carried out at a temperature of 20 to 45°C, preferably 35 to 35°C.
40°C, 11H4, 0-6.0 preferably 5.0-5
.. The test was carried out under the conditions of 5.

また高温消化汚泥を用いる場合には、固定化微生物のj
8養および固定化微生物と石d物含有廃水との接触を温
度45〜60℃好ましくは50〜55℃、+)l−(4
,0〜6.0好ましくは5゜0〜5,5の条件下に行な
う。
In addition, when using high-temperature digested sludge, the immobilized microorganisms
8. The contact between the nutrient and immobilized microorganisms and the wastewater containing stone dwarf is carried out at a temperature of 45 to 60°C, preferably 50 to 55°C, +)l-(4
,0 to 6.0, preferably 5.0 to 5.5.

微生物の固定化は、ゲル状担体に微生物を包み込む公知
の包括法によりつぎのように行なわれる。すなわちゲル
基剤の水溶液に所定団の微化物菌体を温合した後、この
混合液を冷fJ]vるかあるい(よゲル化剤と接触させ
、生成したゲルを所要り′イズの粒状もしくは膜状に成
型する。
Immobilization of microorganisms is carried out as follows by a known entrapping method in which microorganisms are wrapped in a gel-like carrier. That is, after warming a predetermined group of microbial cells in an aqueous solution of a gel base, this mixture is brought into contact with a cold gelling agent, and the resulting gel is heated to the desired size. Form into granules or films.

また、ゲル基質としてポリアクリルアミドを用いる場合
には、所定最の微生物菌体を含む溶液にアクリルアミド
モノマー、itg剤、m合促進剤、重合開始剤を加えて
七ツマ−を重合させ、生成したゲルを上述のように成型
する。ゲル基剤としては、カラギーナン、アルギン酸ソ
ーダ、ポリビニルアルコール、ポリアクリルアミド、ポ
リウレタンなどが用いられ、ゲル化剤としては塩化カリ
ウム、塩化カルシウム、塩化マグネシウムなどが用いら
れ、架橋剤としてはN。
In addition, when polyacrylamide is used as a gel substrate, acrylamide monomer, an ITG agent, an m-merization accelerator, and a polymerization initiator are added to a solution containing a predetermined number of microbial cells, and the seven polymers are polymerized to produce a gel. is molded as described above. Carrageenan, sodium alginate, polyvinyl alcohol, polyacrylamide, polyurethane, etc. are used as the gel base, potassium chloride, calcium chloride, magnesium chloride, etc. are used as the gelling agent, and N is used as the crosslinking agent.

N−−メチレンビスアクリルアミドなどが用いられ、組
合促進剤としてはβ−ジメチルアミノプロピオニトリル
などが用いられ、出合開始剤としては過(A酸カリウム
などが用いられる。
N--methylenebisacrylamide or the like is used, β-dimethylaminopropionitrile or the like is used as the combination accelerator, and potassium per(A-ate) or the like is used as the initiator.

固定化微生物と有礪物含打廃水との接触によって有は酸
を生成せしめる発酵は、回分発酵でも連続発酵でもよい
。まlζ光酊櫓としてはは緘攪拌型発酵槽、固定床型発
酵(凸、流動床型発酵槽などが用いられる。
Fermentation in which acid is produced by contacting immobilized microorganisms with waste water containing impregnated substances may be either batch fermentation or continuous fermentation. As the light tower, a stirred fermenter, a fixed bed fermenter (convex, a fluidized bed fermenter, etc.) are used.

有機物含有廃水としては、都市ごみを含む廃水、下水汚
泥、バルブなどのヘドロ、アルコール蒸留廃液などの食
品加工廃水、し尿などが用いられる。
Examples of wastewater containing organic matter include wastewater containing municipal waste, sewage sludge, sludge from valves, food processing wastewater such as alcohol distillation waste, and human waste.

発明の効果 この発明の有關酸生成法によれば、酸生成能を右する微
生物を担体に固定化し、この固定化微生物を増殖させる
ので、(a内の微住物菌体淵度を高めることにより、廃
水の槽内81)留日数を大幅に短縮することができる上
に、固定化微生物の使用により余剰汚泥を減少さぼるこ
とができる。こうしてこの発明によれば、有機物含有廃
水の処理により有用な有機酸を効率よく生成することが
できる。
Effects of the Invention According to the method for producing acidic acid of the present invention, microorganisms that have acid-producing ability are immobilized on a carrier, and the immobilized microorganisms are grown. As a result, the number of days that wastewater remains in the tank (81) can be significantly shortened, and by using immobilized microorganisms, excess sludge can be reduced. Thus, according to the present invention, useful organic acids can be efficiently produced by treating organic matter-containing wastewater.

実施例 つぎにこの発明の実施例を示し、この発明の効果を例証
づ“る。
EXAMPLES Next, examples of the present invention will be shown to illustrate the effects of the present invention.

実施例1 (1)固定化酸生成菌の調製 グルコース359 // 、コーンスチーブリ力−35
+1 /1 、リン酸水素二カリウム3g /I 。
Example 1 (1) Preparation of immobilized acid-producing bacteria
+1/1, dipotassium hydrogen phosphate 3g/I.

リン酸二水素カリウム2g// 、炭酸アンモニウム5
Q /1 、炭酸ナトリウム3o/a、塩化第2鉄・6
水塩19/lよりなる合成廃水を調製し、これを培地と
して用い、この培地において下水処理場の中温消化汚泥
を温度37℃でpH5,0〜5.5で馴養し、得られた
馴養汚泥100RI/を濃縮して20m/とじた。この
濃縮汚泥を、温度40℃に保温した滅菌済み2%カラギ
ーナン水溶液180m/と混合し、混合液を1.51の
0.1M塩化カルシウム水溶液中に滴下した。こうして
酸生成菌を包括した直径約4mn+のビーズ状ゲルを形
成した。
Potassium dihydrogen phosphate 2g//, ammonium carbonate 5
Q/1, sodium carbonate 3o/a, ferric chloride 6
Synthetic wastewater consisting of 19/l of water salt was prepared, and this was used as a culture medium. Medium-temperature digested sludge from a sewage treatment plant was acclimatized in this culture medium at a temperature of 37°C to a pH of 5.0 to 5.5, and the acclimatized sludge obtained was 100 RI/was concentrated to 20 m/bin. This thickened sludge was mixed with 180ml of a sterilized 2% carrageenan aqueous solution kept at a temperature of 40°C, and the mixed solution was dropped into 1.51ml of a 0.1M calcium chloride aqueous solution. In this way, a bead-like gel with a diameter of about 4 mm+ was formed which contained the acid-producing bacteria.

ついで1!1られた固定化菌を上記組成の培地で温度3
7℃でp H5,0〜5.5で24時間培養し、増殖を
行なった。
Then, the immobilized bacteria were incubated in a medium with the above composition at a temperature of 3.
The cells were cultured at 7° C. and pH 5.0 to 5.5 for 24 hours for proliferation.

(2) 有t1111!2の生成 発酵(1!!どして添付図面に示す実容積11の流動床
型発酵(aを用いた。同種はジャケット(1)を有する
小径の流動部(2)と、これの上にif!なる菌体沈降
用の大径の沈降部(3)とを主体とし、流動部(2)に
は温度およびp l−1の制御表示装置(4)が設けら
れ、沈降部(3)には発生したガスをy1酵液から分離
させる円筒状のガス分離部材(5)が内装されている。
(2) Production fermentation of 1111!2 (1!! and fluidized bed fermentation (a) with an actual volume of 11 as shown in the attached drawing was used. The same type has a small diameter fluidized section (2) with a jacket (1) and a large-diameter sedimentation section (3) for bacterial cell sedimentation called if! on top of this, and a temperature and p l-1 control display device (4) is provided in the flow section (2). A cylindrical gas separation member (5) for separating the generated gas from the y1 fermentation liquid is installed in the sedimentation section (3).

そして有機物含有廃水は槽底部に供給され、処理廃水は
槽頂部からオーバーフローせられる。また槽頂部の廃水
の一部は槽底部に循環され、発生したガスの含mは湿式
ガスメータく6)で測定される。
The organic matter-containing wastewater is then supplied to the bottom of the tank, and the treated wastewater is overflowed from the top of the tank. A portion of the waste water at the top of the tank is circulated to the bottom of the tank, and the content of the generated gas is measured using a wet gas meter 6).

上記溝成の発酵槽を上記固定化酸生成菌と上記合成廃水
で満たし、温度37℃でpH5,0〜5.5で1日回分
発酵を行なった後、合成廃水を連続供給して、連続発酵
を行なった。そして合成廃水の供給mを徐々に増し行っ
たところ、有機物負荷を最大で350Kg/l113−
dayまで上げることができ、8i1留時間2.6時間
においても、有機酸を温度約13(1/1で生成するこ
とができた。
The Mizonari fermenter was filled with the immobilized acid-producing bacteria and the synthetic wastewater, and fermentation was carried out for one day at a temperature of 37°C and a pH of 5.0 to 5.5. After that, the synthetic wastewater was continuously supplied, and the synthetic wastewater was continuously supplied. Fermentation was carried out. Then, by gradually increasing the amount of synthetic wastewater supplied, the organic matter load reached a maximum of 350 kg/l113-
Even at an 8i1 distillation time of 2.6 hours, organic acids could be produced at a temperature of about 13 days (1/1).

実施例2 (1)固定化酸生成菌の調製 下水処理呪の中温消化汚泥をアルコール蒸留廃液で温度
37℃でpH5,0〜5.5で馴養し、得られた馴養汚
泥1001/を1!縮して20allとした。この濃縮
汚泥を、′fiA度40℃に保温した滅菌済み4%カラ
ギーナン水溶液18Ql/と混合し、混合液を1.51
の2%塩化カリウム水溶液中に滴下しlζ。こうして酸
生成菌を包括した直径約4mmのビーズ状ゲルを形成し
た。
Example 2 (1) Preparation of immobilized acid-producing bacteria Medium-temperature digested sludge from sewage treatment was acclimatized with alcohol distillation waste liquid at a temperature of 37°C and pH 5.0 to 5.5, and the obtained acclimatized sludge 1001/1. It was reduced to 20all. This thickened sludge was mixed with 18Ql of a sterilized 4% carrageenan aqueous solution kept at 40°C, and the mixed liquid was
dropwise into a 2% aqueous potassium chloride solution. In this way, bead-shaped gels with a diameter of about 4 mm were formed that contained acid-producing bacteria.

ついで(qられた固定生菌を上記組成の培地で温1f1
37℃でpH5,0〜5.5で24時間培養し、増殖を
行なった。
Then, the fixed live bacteria were incubated at 1f1 in a medium with the above composition.
The cells were cultured at 37° C. and pH 5.0 to 5.5 for 24 hours for proliferation.

なお、アルコール蒸留廃液はフィリピン産廃糖蜜280
Q/lと尿素1.4g//とよりなる培地を用いて24
時間アルコール発酵(酵母サツカロマイセス・セレビエ
シエs accharomyces  cerevis
iac  IFOO224)を行なった後、発酵液を約
4時間に煮沸してアルコールを飛散させることにより得
られた廃液である。この廃液のBODは33000II
1g/lであった。
The alcohol distillation waste liquid is 280% molasses from the Philippines.
24 using a medium consisting of Q/l and 1.4 g// of urea.
Time-alcoholic fermentation (yeast accharomyces cerevisiae)
This is a waste liquid obtained by boiling the fermented liquid for about 4 hours to scatter the alcohol after carrying out the IAC IFOO224). The BOD of this waste liquid is 33000 II
It was 1 g/l.

(2)有8N酸の生成 実容積21の機械攪拌型発酵槽に上記固定化酸生成菌と
上記アルコール蒸留廃液を入れて総容積を11とし、攪
拌下に温度37℃でpH5゜0〜5.5で24時門口分
発酵を行なった。ついで上記アルコール蒸留廃液を連続
供給して連続発酵を行ない、同廃液の供給量を徐々に増
して行ったところ、BOD容槓負荷を最大で102KO
/II+3 ・dayまで上げることができ、有別酸を
温度約100 /1で生成することができた。
(2) Production of 8N acid In a mechanically stirred fermenter with an actual volume of 21, the above-mentioned immobilized acid-producing bacteria and the above-mentioned alcoholic distillation waste liquid were put into a total volume of 11, and the pH was 5°0 to 5 at a temperature of 37°C with stirring. Fermentation was carried out for 24 hours at a temperature of .5. Next, continuous fermentation was carried out by continuously supplying the above alcohol distillation waste liquid, and the supply amount of the waste liquid was gradually increased. As a result, the BOD volume was increased to a maximum of 102 KO.
/II+3 ·day, and a specific acid could be produced at a temperature of approximately 100/1.

実施例3 (1)固定化酸生成菌の調製 実施例1で示した合成廃水を用いて、下水処理場の高温
消化汚泥を温度51℃でf) H5,0〜5.5で馴養
し、得られた馴養汚泥1001Iを濃縮して20+11
/とじた後、この濃縮汚泥を滅菌済み生理食塩水140
01/中に懸濁した。
Example 3 (1) Preparation of immobilized acid-producing bacteria Using the synthetic wastewater shown in Example 1, high-temperature digested sludge from a sewage treatment plant was acclimatized at a temperature of 51°C to f) H5.0 to 5.5, The obtained acclimatized sludge 1001I was concentrated to 20+11
/ After binding, this thickened sludge is diluted with sterilized physiological saline (140 ml).
01/.

(qられた酸生成菌懸濁液にアクリルアミドモノマー1
5gとN、N−メチレンビスアクリルアミド0.89を
混合し、ざらに5%β−ジメチルアミンプロピオニトリ
ル20+1/と2,5%過硫酸カリウム20+11/を
添加した。ついで混合液を10cmx 10cmのバッ
ト4枚にそれぞれ注入し、温度25℃で15分間放置し
、モノマーの出合によりポリアクリルアミドゲルを10
 。
(Acrylamide monomer 1 was added to the acid-producing bacterial suspension.)
5 g and 0.89 g of N,N-methylenebisacrylamide were mixed, and 5% β-dimethylamine propionitrile 20+1/2 and 2.5% potassium persulfate 20+11/ were added to a colander. Next, the mixed solution was injected into four 10 cm x 10 cm vats, and left at a temperature of 25°C for 15 minutes.
.

このゲルを一辺約5mmの立方体にt、uyrした。こ
うして酸生成菌を固定化した。
This gel was shaped into a cube with a side of about 5 mm. In this way, acid-producing bacteria were immobilized.

ついで得られた固定化菌を上記合成廃水で温度51℃で
p H5,O〜5.5で24時間培養し、増殖を行なっ
た。
Then, the obtained immobilized bacteria were cultured in the above synthetic wastewater at a temperature of 51° C. and a pH of 5,0 to 5.5 for 24 hours to perform proliferation.

(2)有鵬酸の生理 実容積2Iの礪械攪拌型発酵(aに上記固定化酸生成菌
と上記合成廃水を入れて、総容積を11とし、攪拌下に
温度51℃で1)H5,0〜5゜5で24時間回分発B
を行なった。ついで上記合成廃水を連続供給して連続発
酵を行ない、同廃液の供給量を徐々に増して行ったとこ
多声装動負荷を最大で180Kg/m ’  ・day
まで上げることができ、安定した連続運転で有礪酸を温
度約9g//で生成することができた。
(2) Mechanically stirred fermentation with a physiological actual volume of 2I of Aiho acid (Pour the above-mentioned immobilized acid-producing bacteria and the above-mentioned synthetic wastewater into a to make a total volume of 11, and under stirring at a temperature of 51°C 1) H5 , 24-hour batch production at 0-5°5 B
I did it. Next, continuous fermentation was carried out by continuously supplying the above synthetic wastewater, and the supply amount of the wastewater was gradually increased, resulting in a polyphonic dynamic load of up to 180 kg/m'・day.
It was possible to generate silicic acid at a temperature of about 9 g// with stable continuous operation.

実施例4 (1)固定化酸生成菌の調製 下水処理場の高温消化力dこを実施例1で説明したアル
コール烹留廃液で温度51℃でpH5゜0〜5.5で馴
養した。ついで得られた馴養力1100m/を、温度5
0℃に保温したウレタンプレポリマー50gの!@濁液
に添加し、両者をよく混合してポリウレタンゲルを得、
このゲルを一辺約511111の立方体に切断した。こ
うして酸生成菌を固定化した。
Example 4 (1) Preparation of immobilized acid-producing bacteria High-temperature digestive bacteria from a sewage treatment plant were acclimatized with the alcohol distilled waste liquid described in Example 1 at a temperature of 51° C. and a pH of 5.0 to 5.5. Then, the obtained acclimatization power of 1100 m/
50g of urethane prepolymer kept at 0℃! @Add to the suspension and mix both well to obtain a polyurethane gel.
This gel was cut into cubes of approximately 511,111 sides. In this way, acid-producing bacteria were immobilized.

ついで得られた固定他国を上記組成の培地で温度51℃
でpH15,0〜5.5で24時間培養し、増殖を行な
った。
Then, the obtained fixed medium was incubated at a temperature of 51°C in a medium with the above composition.
The cells were cultured for 24 hours at pH 15.0 to 5.5 for proliferation.

(2)有儂酸の生成 実容積11の固定床型発酵槽に上記固定化酸生成菌を充
填するとともに上記アルコール蒸留廃液を入れ、温度5
1℃でpH5,0〜5.5で24時間回分発酵を行なっ
た。ついで上記アルコール蒸留廃液を連続供給して連続
発酵を行ない、同廃液の供給mを徐々に増して行ったと
ころ、BOD容槓負荷を最大で約120Ko /l11
3  ・dayまで上げることができ、安定した連続運
転で有磯酸を温度約99//で生成することができた。
(2) Production of elic acid A fixed bed type fermenter with an actual volume of 11 is filled with the above immobilized acid producing bacteria and the above alcohol distillation waste liquid, and the temperature is 5.
Batch fermentation was carried out at 1° C. and pH 5.0 to 5.5 for 24 hours. Next, continuous fermentation was carried out by continuously supplying the above-mentioned alcohol distillation waste liquid, and the supply m of the waste liquid was gradually increased. As a result, the BOD volume ram load reached a maximum of about 120 Ko/l11.
It was possible to increase the temperature up to 3 days, and produce aisoic acid at a temperature of about 99% in stable continuous operation.

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

図面は実施例1において用いた流動床型発酵槽の縦断面
図である。 (2)・・・流動部ζ (3)・・・沈降部、(5)・
・・ガス分離部材。 以上 外4名
The drawing is a longitudinal cross-sectional view of the fluidized bed fermenter used in Example 1. (2)...Flowing part ζ (3)...Settling part, (5)...
...Gas separation member. 4 people other than above

Claims (6)

【特許請求の範囲】[Claims] (1)担体に固定化した酸生成能を有する微生物を培養
して増殖させ、ついで固定化微生物を有機物含有廃水と
接触させることを特徴とする固定化微生物による有機酸
生成法。
(1) A method for producing organic acids using immobilized microorganisms, which comprises culturing and proliferating microorganisms immobilized on a carrier and capable of producing acids, and then bringing the immobilized microorganisms into contact with wastewater containing organic matter.
(2)温度20〜45℃、pH4.0〜6.0の条件下
に操作を行なう特許請求の範囲1項記載の方法。
(2) The method according to claim 1, wherein the operation is carried out at a temperature of 20 to 45°C and a pH of 4.0 to 6.0.
(3)温度35〜40℃、pH5.0〜5.5の条件下
に操作を行なう特許請求の範囲第2項記載の方法。
(3) The method according to claim 2, wherein the operation is carried out at a temperature of 35 to 40°C and a pH of 5.0 to 5.5.
(4)温度45〜60℃、pH4.0〜6.0の条件下
に操作を行なう特許請求の範囲第1項記載の方法。
(4) The method according to claim 1, wherein the operation is carried out at a temperature of 45 to 60°C and a pH of 4.0 to 6.0.
(5)温度50〜55℃、pH5.0〜5.5の条件下
に操作を行なう特許請求の範囲第4項記載の方法。
(5) The method according to claim 4, wherein the operation is carried out at a temperature of 50 to 55°C and a pH of 5.0 to 5.5.
(6)微生物の固定化を包括法により行なう特許請求の
範囲第1〜5項のうちいずれか1項記載の方法。
(6) The method according to any one of claims 1 to 5, wherein the immobilization of microorganisms is carried out by an entrapment method.
JP59177167A 1984-08-24 1984-08-24 Production of organic acid by immobilized microorganism Granted JPS6156087A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59177167A JPS6156087A (en) 1984-08-24 1984-08-24 Production of organic acid by immobilized microorganism

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59177167A JPS6156087A (en) 1984-08-24 1984-08-24 Production of organic acid by immobilized microorganism

Publications (2)

Publication Number Publication Date
JPS6156087A true JPS6156087A (en) 1986-03-20
JPS6324678B2 JPS6324678B2 (en) 1988-05-21

Family

ID=16026354

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59177167A Granted JPS6156087A (en) 1984-08-24 1984-08-24 Production of organic acid by immobilized microorganism

Country Status (1)

Country Link
JP (1) JPS6156087A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002028693A (en) * 2000-07-14 2002-01-29 Kurabo Ind Ltd Method for treating alkaline wastewater
WO2008000809A1 (en) * 2006-06-30 2008-01-03 Biogasol Ipr Aps Production of fermentation products in biofilm reactors using microorganisms immobilised on sterilised granular sludge
JP2012076000A (en) * 2010-09-30 2012-04-19 Kuraray Co Ltd One tank type anaerobic wastewater treatment apparatus

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002028693A (en) * 2000-07-14 2002-01-29 Kurabo Ind Ltd Method for treating alkaline wastewater
WO2008000809A1 (en) * 2006-06-30 2008-01-03 Biogasol Ipr Aps Production of fermentation products in biofilm reactors using microorganisms immobilised on sterilised granular sludge
JP2012076000A (en) * 2010-09-30 2012-04-19 Kuraray Co Ltd One tank type anaerobic wastewater treatment apparatus

Also Published As

Publication number Publication date
JPS6324678B2 (en) 1988-05-21

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