JPH0783708B2 - Algae culture device - Google Patents

Algae culture device

Info

Publication number
JPH0783708B2
JPH0783708B2 JP32299992A JP32299992A JPH0783708B2 JP H0783708 B2 JPH0783708 B2 JP H0783708B2 JP 32299992 A JP32299992 A JP 32299992A JP 32299992 A JP32299992 A JP 32299992A JP H0783708 B2 JPH0783708 B2 JP H0783708B2
Authority
JP
Japan
Prior art keywords
algae
tank
culture
culture tank
algae culture
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 - Lifetime
Application number
JP32299992A
Other languages
Japanese (ja)
Other versions
JPH06165668A (en
Inventor
曠世 松本
彰弘 浜崎
正 辻
英司 後藤
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP32299992A priority Critical patent/JPH0783708B2/en
Publication of JPH06165668A publication Critical patent/JPH06165668A/en
Publication of JPH0783708B2 publication Critical patent/JPH0783708B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M21/00Bioreactors or fermenters specially adapted for specific uses
    • C12M21/02Photobioreactors
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M29/00Means for introduction, extraction or recirculation of materials, e.g. pumps
    • C12M29/18External loop; Means for reintroduction of fermented biomass or liquid percolate
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M31/00Means for providing, directing, scattering or concentrating light
    • C12M31/08Means for providing, directing, scattering or concentrating light by conducting or reflecting elements located inside the reactor or in its structure
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M39/00Means for cleaning the apparatus or avoiding unwanted deposits of microorganisms
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12MAPPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
    • C12M43/00Combinations of bioreactors or fermenters with other apparatus
    • C12M43/04Bioreactors or fermenters combined with combustion devices or plants, e.g. for carbon dioxide removal

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Genetics & Genomics (AREA)
  • Biotechnology (AREA)
  • Sustainable Development (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Combustion & Propulsion (AREA)
  • Molecular Biology (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Light Guides In General And Applications Therefor (AREA)

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は微細藻類の培養装置に関
する。
FIELD OF THE INVENTION The present invention relates to a culture apparatus for microalgae.

【0002】[0002]

【従来の技術】有価物の大量生産または廃棄ガス中のC
2 の大量処理を目的に、クロレラなどの微細藻類の利
用が考えられており、そのための藻類培養槽もいくつか
提案されていて、光ファイバを利用した培養槽もその一
つである。藻類培養において、藻類の光ファイバ上や槽
内壁への付着は光利用効率の低下、藻類培養槽内の微生
物汚染の原因などを引き起こすので大きな問題であり、
付着対策が種々行われている。その対策の一例を図3に
よって説明する。
2. Description of the Related Art Mass production of valuables or C in waste gas
The use of microalgae such as chlorella has been considered for the purpose of large-scale treatment of O 2 , and several algae culture tanks have been proposed for that purpose, and a culture tank using an optical fiber is one of them. In algae culture, adhesion of algae on the optical fiber or to the inner wall of the tank is a big problem because it causes a decrease in light utilization efficiency and causes microbial contamination in the algae culture tank.
Various anti-adhesion measures are taken. An example of the countermeasure will be described with reference to FIG.

【0003】図3において、1は培養槽本体、2は側面
出光光ファイバ、3はガス分散口、4は流量計、5はC
2 ガス、6は光源、7は受光口、11はガス出口、1
2は循環ポンプである。培養槽本体1内には微細藻類が
液体培地内に分散され培養されている。藻類は光源6か
ら受光口7を経て側面出光光ファイバ2から得られる光
及び流量計4、ガス分散口3を経て供給されるCO2
ス5より光合成を行い、CO2 の固定及び有価物の生産
を行っている。藻類の付着対策手段としては二つあり、
一つは循環ポンプ12による攪拌手段で、もう一つはガ
ス供給に、注射針を側面出光光ファイバ2の間隙に多数
挿入して微細気泡を発生させ、培養槽本体1内で起こる
気泡の破裂及び合一に伴って発生する超音波の作用によ
り付着した藻類を剥離させる手段である。
In FIG. 3, 1 is a main body of a culture tank, 2 is a side emission optical fiber, 3 is a gas dispersion port, 4 is a flow meter, and 5 is C.
O 2 gas, 6 light source, 7 light receiving port, 11 gas outlet, 1
2 is a circulation pump. In the culture tank body 1, microalgae are dispersed and cultured in a liquid medium. Algae perform photosynthesis from light obtained from the light source 6 through the light receiving port 7 and the side output optical fiber 2 and the CO 2 gas 5 supplied through the flowmeter 4 and the gas dispersion port 3, to fix CO 2 and to recover valuables. It is in production. There are two algae adhesion countermeasures,
One is a stirring means by the circulation pump 12, and the other is a gas supply, in which a large number of injection needles are inserted into the gaps of the side surface optical output fibers 2 to generate fine bubbles, and the bubbles burst in the culture tank body 1. And a means for peeling off the algae attached by the action of ultrasonic waves generated by the coalescence.

【0004】[0004]

【発明が解決しようとする課題】上述した付着対策手段
では下記理由により完全に付着防止ができない。 (1)ポンプによる攪拌は培養槽内の淀みの部分の攪拌
はできない(培養槽内の淀みを完全に無くすことはでき
ない)。 (2)気泡注入口より下は超音波の作用が期待できない
ので、一旦付着が生じればそれを剥離させることはでき
ない。
The above-mentioned means for preventing adhesion cannot completely prevent adhesion due to the following reasons. (1) Stirring with a pump cannot stir the stagnation portion in the culture tank (the stagnation in the culture tank cannot be completely eliminated). (2) Since the action of ultrasonic waves cannot be expected below the bubble injection port, once adhesion occurs, it cannot be peeled off.

【0005】本発明は上記技術水準に鑑み、微細藻類培
養槽本体内で光ファイバや槽内壁に藻類の付着が生ぜ
ず、従って藻類の増殖を順調に行ない得る微細藻類培養
装置を提供しようとするものである。
In view of the above-mentioned state of the art, the present invention intends to provide a microalgae culture apparatus which does not cause algae to adhere to the optical fiber or the inner wall of the tank in the main body of the microalgae culture tank and therefore can smoothly grow the algae. It is a thing.

【0006】[0006]

【課題を解決するための手段】本発明は食糧、機能性食
品などの有価物の大量生産または廃棄ガス中のCO2
大量処理用の光ファイバを利用した藻類培養槽、該藻類
培養槽の容積よりも大容量の保管槽、所定時間毎に藻類
培養槽内の全内容物を保管槽に移送させる配管及び所定
時間毎に保管槽に貯えられた内容物を藻類培養槽の上部
より藻類培養槽内に落下供給する配管を具備してなる藻
類培養装置である。
The present invention relates to an algae culture tank using an optical fiber for mass production of valuables such as foods and functional foods, or for large-scale treatment of CO 2 in waste gas. A storage tank with a capacity larger than the volume, a pipe for transferring all the contents in the algae culture tank to the storage tank at a predetermined time, and the contents stored in the storage tank at a predetermined time from the upper part of the algae culture tank It is an algae culture device equipped with a pipe for dropping and supplying it into a tank.

【0007】本発明装置をさらに具体的に説明すると、
藻類培養槽とは別に、それよりも大容量の保管槽を設
け、藻類培養槽と保管槽との間に、内容物を下記のよう
に移動させるように構成したものである。
More specifically, the device of the present invention will be described.
A storage tank having a larger capacity than that of the algae culture tank is provided, and the contents are moved between the algae culture tank and the storage tank as follows.

【0008】タイマーを利用し一定の時間間隔で、培養
槽内の培地を保管槽にポンプにて汲み上げ培養槽内を空
にし、培養槽内が空になればポンプを停止し、保管槽内
の内容物を自然落下もしくはポンプにて培養槽内に培地
を注入させるようにしたものである。
The medium in the culture tank is pumped up to the storage tank by a pump at a certain time interval using a timer to empty the culture tank, and when the culture tank is empty, the pump is stopped and the storage tank The contents are naturally dropped or a medium is injected into the culture tank by a pump.

【0009】なお、時間間隔は藻類の付着状況により
2,3分間隔から数時間まで状況による。付着しやすい
藻類の場合は2,3分間隔で運転を行なう。通常の付着
しにくい藻類の場合でも液性の変化などが原因で付着が
始まると、2〜3日の短期間で目に見えるほどの広さに
まで付着が成長するので、初期付着物除去のために数時
間間隔の運転が必要である。培地の培養槽内への注入方
法は自然落下によるもののほうが簡便であるが、藻類の
付着状況により強力な水流が必要とされる場合にはポン
プを使用するのが好ましい。
The time interval varies from a few minutes to several hours depending on the algae adhesion condition. For algae that tend to adhere, run every few minutes. Even in the case of normal algae that are difficult to attach, if attachment begins due to changes in liquidity, etc., the attachment grows to a visible extent within a short period of 2 to 3 days. Therefore, it is necessary to operate at intervals of several hours. The method of injecting the medium into the culture tank is simpler by spontaneous dropping, but it is preferable to use a pump when a strong water flow is required due to the algae adhesion state.

【0010】[0010]

【作用】培養槽内での藻類の付着は初期の段階では、水
流(水しぶき)をあてるだけで簡単に剥離させることが
できる。そこで、一度培養槽内の培地を完全に抜くこと
により藻類付着部を露出させ次に、培地を再注入すると
きにできる水流に付着部がさらされる状態をつくること
により付着した藻類を剥離させることができる。この繰
り返しで藻類の付着を防止できる。
In the initial stage, the adhesion of algae in the culture tank can be easily separated by applying a water stream (spray). Therefore, once the culture medium in the culture tank is completely removed to expose the algae attachment part, and then to remove the algae attachment by creating a state where the attachment part is exposed to the water flow that can be performed when re-injecting the culture medium. You can By repeating this, adhesion of algae can be prevented.

【0011】[0011]

【実施例】本発明の一実施例を図1によって説明する。
図1において、符号1〜7及び11は図3と同一のもの
を意味するので説明は省略する。8はポンプ、9はタイ
マー、10は保管槽、13は電磁弁を示す。
DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the present invention will be described with reference to FIG.
In FIG. 1, reference numerals 1 to 7 and 11 mean the same as those in FIG. 8 is a pump, 9 is a timer, 10 is a storage tank, and 13 is a solenoid valve.

【0012】図1の培養層本体1内に、培地を調整し種
藻類を100mg/リットル投入し藻類を増殖させた。
次に述べる方法を5分間隔で付着防止のために行った。 (1)排出ポンプ8で培養槽本体1内の培地を保管槽1
0に排出する。この時は電磁弁13は閉にする。 (2)排出が1分以内に終了するので排出ポンプ8を停
止させる(タイマー9を利用)。 (3)タイマー9で電磁弁13を開け、自然落下により
保管槽10内の培地を培養槽本体1に再注入させる。
In the culture layer body 1 shown in FIG. 1, the medium was adjusted and seed algae was added at 100 mg / liter to grow the algae.
The following method was carried out at intervals of 5 minutes to prevent adhesion. (1) The storage tank 1 for storing the medium in the culture tank main body 1 by the discharge pump 8.
Discharge to 0. At this time, the solenoid valve 13 is closed. (2) Since the discharging is completed within 1 minute, the discharging pump 8 is stopped (using the timer 9). (3) The solenoid valve 13 is opened by the timer 9 and the culture medium in the storage tank 10 is reinjected into the culture tank main body 1 by spontaneous fall.

【0013】上記運転結果を図2に示す。図2より明ら
かなように、この実施例装置では培養槽本体1の側面出
光光ファイバ2、培養槽本体1の側壁には付着物は全く
認められず、培養2日目の300mg/リットルから培
養期間6日間の濃度も約3000mg/リットルと順調
に増殖していた。
The results of the above operation are shown in FIG. As is clear from FIG. 2, in the apparatus of this embodiment, no adherent matter was observed on the side surface optical output fiber 2 of the culture tank body 1 and the side wall of the culture tank body 1, and the culture was started from 300 mg / liter on the second day of culture. The concentration for 6 days was about 3000 mg / liter, and the cells were growing well.

【0014】これに対し、図3に示した従来の培養槽で
は図4に示すように運転結果であった。図4から明らか
なように、藻体濃度(培地中)が殆んど増殖しておら
ず、初期濃度300mg/リットルから培養6日間で1
000mg/リットルまでしか増殖していなかった。し
かし、試験終了時に側面出光光ファイバ2やガス分散口
3などに付着した藻類を掻き落として藻体濃度に換算す
ると約2000mg/リットルであった。すなわち、培
地中に分散している藻類に対して倍程度の藻体付着であ
った。
On the other hand, in the conventional culture tank shown in FIG. 3, the operation result was as shown in FIG. As is clear from FIG. 4, almost no algal cell concentration (in the medium) grew, and the initial concentration was 300 mg / liter, and it was 1 after 6 days of culture.
It had grown only up to 000 mg / l. However, when the test was completed, the algae adhering to the side surface optical output fiber 2 and the gas dispersion port 3 were scraped off and converted to an algal cell concentration of about 2000 mg / liter. That is, the adhesion of algal cells was about twice that of the algae dispersed in the medium.

【0015】以上の結果より、本発明装置は従来の微細
藻類培養装置に比較し、藻類の培養槽内の付着対策とし
ては著しく効果があることが明らかである。
From the above results, it is clear that the device of the present invention is remarkably effective as a countermeasure against adhesion of algae in the culture tank, as compared with the conventional microalgae culture device.

【0016】[0016]

【発明の効果】本発明装置によれば、微細藻類培養に際
し培養槽本体内への微細藻類の付着量は著しく低減で
き、微細藻類の順調な培養増殖が可能となる。
According to the apparatus of the present invention, the amount of microalgae adhered to the main body of the culture tank during the culture of microalgae can be remarkably reduced, and the microalgae can be smoothly cultured and grown.

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

【図1】本発明装置の一実施例の説明図。FIG. 1 is an explanatory view of an embodiment of the device of the present invention.

【図2】本発明装置による一実施例の微細藻類の増殖結
果を示す図表。
FIG. 2 is a chart showing the results of the growth of microalgae in one example by the device of the present invention.

【図3】従来の微細藻類の培養装置の一態様の説明図。FIG. 3 is an explanatory diagram of one embodiment of a conventional culture apparatus for microalgae.

【図4】従来の微細藻類による微細藻類の増殖結果を示
す図表。
FIG. 4 is a chart showing the results of growth of microalgae by conventional microalgae.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 食糧、機能性食品などの有価物の大量生
産または廃棄ガス中のCO2 の大量処理用の光ファイバ
を利用した藻類培養槽、該藻類培養槽の容積よりも大容
量の保管槽、所定時間毎に藻類培養槽内の全内容物を保
管槽に移送させる配管及び所定時間毎に保管槽に貯えら
れた内容物を藻類培養槽の上部より藻類培養槽内に落下
供給する配管を具備してなる藻類培養装置。
1. An algae culture tank using an optical fiber for mass production of valuables such as foods and functional foods or mass treatment of CO 2 in waste gas, and storage of a larger volume than the volume of the algae culture tank. A tank, a pipe for transferring all the contents in the algae culture tank to the storage tank at a predetermined time, and a pipe for dropping the contents stored in the storage tank at a predetermined time from the upper part of the algae culture tank into the algae culture tank An algae culture device comprising:
JP32299992A 1992-12-02 1992-12-02 Algae culture device Expired - Lifetime JPH0783708B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32299992A JPH0783708B2 (en) 1992-12-02 1992-12-02 Algae culture device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32299992A JPH0783708B2 (en) 1992-12-02 1992-12-02 Algae culture device

Publications (2)

Publication Number Publication Date
JPH06165668A JPH06165668A (en) 1994-06-14
JPH0783708B2 true JPH0783708B2 (en) 1995-09-13

Family

ID=18150011

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32299992A Expired - Lifetime JPH0783708B2 (en) 1992-12-02 1992-12-02 Algae culture device

Country Status (1)

Country Link
JP (1) JPH0783708B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8541225B2 (en) * 2011-07-25 2013-09-24 General Atomics System and method for using a pulse flow circulation for algae cultivation
CN108034574A (en) * 2017-09-19 2018-05-15 中国水产科学研究院南海水产研究所 Deep water type microalgae culture system

Also Published As

Publication number Publication date
JPH06165668A (en) 1994-06-14

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