JPS61185180A - Immobilized bioreactor for alcoholic fermentation - Google Patents

Immobilized bioreactor for alcoholic fermentation

Info

Publication number
JPS61185180A
JPS61185180A JP2452885A JP2452885A JPS61185180A JP S61185180 A JPS61185180 A JP S61185180A JP 2452885 A JP2452885 A JP 2452885A JP 2452885 A JP2452885 A JP 2452885A JP S61185180 A JPS61185180 A JP S61185180A
Authority
JP
Japan
Prior art keywords
gas
reactor
bioreactor
separation zone
immobilized
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.)
Pending
Application number
JP2452885A
Other languages
Japanese (ja)
Inventor
Yuji Yasuda
雄二 保田
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.)
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 JP2452885A priority Critical patent/JPS61185180A/en
Publication of JPS61185180A publication Critical patent/JPS61185180A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To keep high volume efficiency of an immobilized bioreactor, to facilitate the removal of generated gas, and to prevent the loss of immobilization carrier, by attaching common gas-liquid separation zone to the top of a coil, and separating and removing generated CO2 gas with the separation zone. CONSTITUTION:A common gas-liquid separation zone 4 is attached to the top of a coil. A number of cell-immobilization carrier particles are suspended in a reactor, and the fermentable saccharide in the raw syrup supplied from the line 1 is decomposed to produce ethanol. The separation of the generated gas bubbles can be carried out surely in improved efficiency by the use of the gas- liquid separation zone, and the loss of the immobilization carrier accompanied by the fermentation liquid flow in the line 5 can be prevented.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、アルコール発酵用の固定化バイオリアクター
に関し、特に連続発酵による固定化バイオリアクターに
関する。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to an immobilized bioreactor for alcohol fermentation, and in particular to an immobilized bioreactor with continuous fermentation.

(従来の技術) 発酵法によるアルコール製造は、従来、いわゆる醸造業
を中心にして発達してきているが、近年、この技術をベ
ースに、農産物などいわゆるバイオマス(糖蜜、さつま
いも、とうもろこし、さとうきびなど)から燃料用アル
コール(と<Kエタノール)を製造し、これをガソリン
等従来からある燃料に混入して使用するいわゆる°ガソ
ホール計画″などが企画されている。
(Conventional technology) Alcohol production by fermentation has traditionally been developed mainly in the so-called brewing industry, but in recent years, based on this technology, it has been possible to produce alcohol from so-called biomass such as agricultural products (molasses, sweet potatoes, corn, sugar cane, etc.). The so-called "gasohol project" is being planned, in which fuel alcohol (and <K ethanol) is produced and used by mixing it with conventional fuels such as gasoline.

ブラジルなどではすでに実現し、エタノール8産100
 K/規模のプラントも稼動しているが、今後東南アジ
アなど開発途上国を中心にこの計画が普及していく気運
にある。
This has already been achieved in countries such as Brazil, where 80% of ethanol can be produced.
K/scale plants are also in operation, and there are signs that this plan will become more popular in developing countries, such as Southeast Asia.

従来、醸造業を中心に発達した発酵プロセスは、大容量
の発酵槽が多段基必要で、回分式であるためエタノール
生産性(発酵槽単位容量当り、単位時間当りのエタノー
ル生産量)は高々1〜2 kgエタノール/m”/hで
あり、これを改良した菌体再循環半連続発酵法(Mal
e−Boinot法)でも高々4kg/mj/hKすぎ
ない。
Traditionally, the fermentation process developed mainly in the brewing industry requires large-capacity fermenters in multiple stages and is a batch process, so the ethanol productivity (ethanol production per unit capacity of fermenter, per unit time) is at most 1. ~2 kg ethanol/m”/h, and an improved bacterial cell recirculation semi-continuous fermentation method (Mal
Even with the e-Boinot method, it is no more than 4 kg/mj/hK.

一方、bまだ実用化はされていないが、これら従来法の
欠点を克服することを企図して、各種の新しいバイオリ
アクター、例えば、菌体を固定化(固定化法には、アル
ギン酸ンーダを用いる包括法など各種の方法がある)し
て連続発酵を行う反応器(すなわち、固定化バイオリア
クター)などが次々と開発されているが、いまだ、確立
されたものとけ言えない。
On the other hand, although it has not yet been put to practical use, various new bioreactors have been proposed to overcome the drawbacks of these conventional methods, such as immobilization of bacterial cells (the immobilization method uses alginate powder). Reactors (i.e., immobilization bioreactors) that carry out continuous fermentation using various methods (including the comprehensive method) have been developed one after another, but it cannot be said that they have been established yet.

(発明が解決しようとす東問題点) 上記した現状において提案されている固定化バイオリア
クターKd、次の基本的問題点がある0 (1) アルコール発酵の結果、大量に副生するCOl
 ガスによって、リアクター内は強混合状態にあり、し
たがって、リアクター混合型式を「押出し流れ系」K近
づけることが困難で、そのため発酵槽容積効率(=エタ
ノール生産性)向上が妨げられている。(現状の固定化
バイオリアクター混合型式はほぼ完全混合系であシ、押
出し流れ系に比べると同一反応収率=エタノール生成!
/糖基質消費量をうるKきわめて長時間の反応時間を要
し、アルコール生産性=容積効率が低くなる。) (2)  副生CO2ガス気泡は「発酵産物」であるた
めきわめて微細で、リアクター内液中から排除されにく
く、それがために■リアクターから固定化担体(吸着法
や包括法等によシ菌を固定化した物体)が発酵液ととも
に随伴流出されやすく(リアクター内固定化担体量がし
だいに減少して、連続発酵の定常状態が保ちにくくなる
)、■固定化担体表面に微細気泡が付着して基質や生成
物の移動を妨害し、結果的に固定化担体を失活せしめる
、などの不具合がある0上記(IIKついては、固定化
担体を反応器内に高密度で充填して原料糖液を上方また
は下方から流し極力押出し流れ系に維持しようとする「
充填層型反応器」もあるが、この方式ではりアクタ−内
の偏流が起きやすく(生成エタノールやCO,の局部的
蓄積がおき担体が失活する)、また発生CO,ガスによ
って、いずれにしても相当の混合があるので、担体充填
密度がきわめて高いこの方式では、固定化担体に対する
剪断力(Shearing Force)も大となり、
固定化担体の損傷が起きやすいなどの問題があって現実
にはあまり採用されない。
(Problems that the invention seeks to solve) The immobilization bioreactor Kd proposed in the above-mentioned current situation has the following basic problems. (1) As a result of alcohol fermentation, a large amount of COl is produced as a by-product.
Due to the gas, the interior of the reactor is in a strong mixing state, and therefore it is difficult to bring the reactor mixing type close to the "extrusion flow system" K, which hinders improvement in fermenter volumetric efficiency (=ethanol productivity). (The current immobilized bioreactor mixing system is a nearly complete mixing system, and compared to the extrusion flow system, the same reaction yield = ethanol production!
/ Obtaining sugar substrate consumption requires an extremely long reaction time, resulting in low alcohol productivity = volumetric efficiency. ) (2) Because the by-product CO2 gas bubbles are "fermentation products," they are extremely fine and difficult to remove from the reactor internal liquid. (objects with immobilized bacteria) are likely to flow out together with the fermentation liquid (the amount of immobilized carriers in the reactor gradually decreases, making it difficult to maintain a steady state of continuous fermentation), and ■ microbubbles adhere to the surface of the immobilized carriers. (For IIK, the immobilized carrier is packed in the reactor at a high density and the raw sugar is The liquid is flowed from above or below, trying to maintain the extrusion flow system as much as possible.
There is also a ``packed bed reactor,'' but this method tends to cause uneven flow within the beam reactor (local accumulation of produced ethanol and CO causes deactivation of the carrier), and the generated CO and gas tend to cause uneven flow in the reactor. However, in this method, where the carrier packing density is extremely high, the shearing force on the immobilized carrier is also large.
This method is not often used in practice due to problems such as the possibility of damage to the immobilization carrier.

本発明は、これら従来法の問題点を克服して、高生産性
、高安定性のバイオリアクターを提供することを目的と
するものである。
The present invention aims to overcome the problems of these conventional methods and provide a bioreactor with high productivity and high stability.

(問題点を解決するための手段) 本発明は、上記目的を連続発酵において大量のCO,ガ
ス発生があるにもかかわらず、リアクター内混合型式を
極力押出し流れ系に近づけることKより、高い容積効率
(す・なわち、高いアルコール生産性)を維持し、発生
ガスの排除を容易にし、固定化担体の流失を防止(すな
わち高い安定性を維持)して達成するものである。
(Means for Solving the Problems) The present invention aims to achieve the above-mentioned objective by bringing the mixing type in the reactor as close as possible to the extrusion flow system, even though a large amount of CO and gas are generated in continuous fermentation. This is achieved by maintaining efficiency (ie, high alcohol productivity), facilitating the removal of generated gas, and preventing the immobilized carrier from flowing away (ie, maintaining high stability).

すなわち、本発明は、連続発酵によるアルコール生産用
の固定化バイオリアクターを、(1)横型蛇管式(蛇管
のピッチ賃数は任意に設定しうる)の構造とし、 (2)  この蛇管上部に、発生CO2ガスを分離・排
除する共通の気液分離ゾーンを設ける、ことを特徴とす
る固定化バイオリアクターに関するものである。
That is, the present invention provides an immobilized bioreactor for alcohol production by continuous fermentation, (1) having a structure of a horizontal corrugated tube type (the pitch rate of the corrugated tube can be set arbitrarily), (2) on the upper part of this corrugated tube, The present invention relates to an immobilized bioreactor characterized in that a common gas-liquid separation zone is provided to separate and eliminate generated CO2 gas.

第1図は本発明の固定化バイオリアクターの一実施態様
例を示す図である。本バイオリアクターは、第1図のご
とく横型蛇管式(ピッチ数は、反応動力学特性などに基
づいて任意に設定しうる0すなわち、ピッチ数は、エタ
ノール発酵速度の見晴原料基質濃度依存性ならびに生成
物濃度依存性によシ決まる0濃度依存性が高いほど多段
化すれば、反応器容積効率が高まることKなり、所定の
エタノール生産量を維持するのくコンパクトな反応器で
済む0)で、蛇管の上部に共通の気液分離ゾーン4を設
けである。゛なお、第1図中、1は固定化バイオリアク
タ一本体、2け原料糖液ライン、3は発生CO2ガスラ
イン、5は発岬液ライン、6は固定化担体、7は発生気
泡、8は分離精製工程である。
FIG. 1 is a diagram showing an embodiment of the immobilization bioreactor of the present invention. This bioreactor is a horizontal serpentine type bioreactor as shown in Figure 1 (the number of pitches can be set arbitrarily based on reaction kinetic characteristics, etc.). The higher the concentration dependence, the higher the reactor volumetric efficiency, and the more compact the reactor is needed to maintain the specified ethanol production amount, A common gas-liquid separation zone 4 is provided at the top of the flexible pipe.゛In Fig. 1, 1 is the immobilization bioreactor main body, 2 raw sugar liquid lines, 3 is the generated CO2 gas line, 5 is the cape liquid line, 6 is the immobilization carrier, 7 is the generated bubbles, 8 is a separation and purification process.

(作用・効果) このリアクター内には、菌体固定化担体6が多数浮遊懸
濁しており、ライン1から供給される原料糖液中の発酵
性糖質を分解してエタノールを生産する。
(Function/Effect) A large number of bacterial cell immobilized carriers 6 are suspended in this reactor, and fermentable carbohydrates in the raw sugar solution supplied from line 1 are decomposed to produce ethanol.

なお、菌体固定化法は、包括法や吸着法など各種の方法
があり、包括法の包括剤としては、アルギン酸ソーダ、
K−カラギーナン、Pvム(ポリビニルアルコール)な
ど一般的かつ公知なものが使用され、また吸′着法では
活性アルミナや活性炭等一般的なものが使用される。
There are various methods for immobilizing bacterial cells, such as entrapping method and adsorption method.
Common and well-known materials such as K-carrageenan and Pvum (polyvinyl alcohol) are used, and in the adsorption method, common materials such as activated alumina and activated carbon are used.

このよう忙、蛇管式にすることで、リアクター内混合様
式は押出し流れ系によシ近くなシ、容積効率が著しく向
上する。すなわち、同一のアルコール生産量を維持する
のに小容量の発酵槽ですむ、あるいは、同一容量の発酵
槽で多くのアルコール生産量を保ちうる。
By employing such a flexible pipe type, the mixing mode within the reactor is close to the extrusion flow system, and the volumetric efficiency is significantly improved. In other words, a smaller capacity fermenter can be used to maintain the same amount of alcohol produced, or a larger amount of alcohol can be produced with the same capacity fermenter.

また、これを横型にすることで、リアクターの高さを高
くする必要がなく、シたがって、発生ガスの排除の上か
らも有利となる(リアクターの高さが高いほど、発生気
泡のりアクタ−内滞留時間が長くなり、系外へ抜けK<
くなる)0さらに1蛇管上部に共通の気液分離シー74
を設けることで発生ガス気泡の排除もよシ高効率で、か
つ確実に行われ、ライン5の発酵液による固定化担体の
随伴流出も防止でき、リアクター内固定化担体保持量を
安定的に維持でき、安定性が増す。
In addition, by making this horizontal, there is no need to increase the height of the reactor, which is advantageous in terms of eliminating generated gas (the higher the height of the reactor, the more the bubbles generated will be Residence time inside becomes longer, and K<
) 0 In addition, a common gas-liquid separation seam 74 is installed at the top of the flexible pipe.
By providing this, the generated gas bubbles can be removed more efficiently and reliably, and the accompanying outflow of the immobilized carrier due to the fermentation liquid in line 5 can also be prevented, and the amount of immobilized carrier retained in the reactor can be stably maintained. This increases stability.

(実施例) 第1図で示した本発明の固定化バイオリアクターと、第
2図で示す従来型の固定化バイオリアクターの小型装R
(槽容量は11で同一)を試作し、両者のエタノール生
産性を比較して本発明の有効性を確認した。
(Example) The immobilization bioreactor of the present invention shown in FIG. 1 and the conventional immobilization bioreactor shown in FIG.
(The tank capacity is the same at 11) was prototyped, and the ethanol productivity of both was compared to confirm the effectiveness of the present invention.

第2図中、第1図と同一符号は第1図と合義であり、1
1け固定化バイオリアクター、12は原料貯槽、13は
原料送液ポンプである。
In Figure 2, the same symbols as in Figure 1 have the same meaning as in Figure 1, and 1
1 immobilized bioreactor, 12 a raw material storage tank, and 13 a raw material feed pump.

下表に1本実験で使用した原料糖液の組成を示す。The table below shows the composition of the raw sugar solution used in one experiment.

菌体の固定化方法は両リアクターとも同一とし次のよう
に行った。
The method for immobilizing bacterial cells was the same in both reactors and was carried out as follows.

包括剤はアルギン酸ソーダ3チ水溶液(ゲル化は、Oa
k/、 5チ水溶液を使用)を使用し、球形の固定化担
体としてリアクター内に容量比として25%程度充填し
た。
The encapsulant is a 3-chloride aqueous solution of sodium alginate (for gelation, Oa
A spherical immobilized carrier was used, and the reactor was filled with a volume ratio of about 25%.

また、発酵液pH4,5、温度50°0、使用菌体は8
accharomyces ellipsoideus
  00−2  である。
In addition, the pH of the fermentation liquid was 4.5, the temperature was 50°0, and the number of bacteria used was 8.
accharomyces ellipsoideus
It is 00-2.

両リアクターを希釈率(=原液流量/槽容積で、滞留時
間の逆数で示される)(15h−’で連続運転し、従来
型とエタノール生産性を比較したところ、本発明のバイ
オリアクターでは、従来型の約1.4〜1.5倍の生産
性を維持しうろことが判明するとともに1 リアクター
内の固定化担体保持もきわめて安定的になしうろことも
確認され、本発明の有効性が確認された。
Both reactors were operated continuously for 15 hours at a dilution rate (= stock solution flow rate/tank volume, expressed as the reciprocal of the residence time), and the ethanol productivity was compared with that of the conventional type. It was found that the productivity was approximately 1.4 to 1.5 times higher than that of the mold, and it was also confirmed that the immobilized carrier was retained extremely stably within the reactor, confirming the effectiveness of the present invention. Ta.

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

第1図は本発明リアクターの一実施態様例を示す図、第
2図は従来のバイオリアクターを示す図である。 復代理人  内 1)  明 復代理人  萩 原 亮 − 第1図 第2図 手続補正書
FIG. 1 is a diagram showing an embodiment of the reactor of the present invention, and FIG. 2 is a diagram showing a conventional bioreactor. Sub-agent: 1) Sub-agent: Ryo Hagiwara - Figure 1 Figure 2 Procedure amendment

Claims (1)

【特許請求の範囲】[Claims] 連続発酵によるアルコール生産用固定化バイオリアクタ
ーにおいて、該リアクターを横型蛇管式とし、該蛇管上
部に発生CO_2ガスを分離・排除する共通の気液分離
ゾーンを設けたことを特徴とするアルコール発酵用の固
定化バイオリアクター。
An immobilized bioreactor for alcohol production by continuous fermentation, characterized in that the reactor is of a horizontal serpentine tube type, and a common gas-liquid separation zone for separating and eliminating generated CO_2 gas is provided at the upper part of the serpentine tube. Immobilization bioreactor.
JP2452885A 1985-02-13 1985-02-13 Immobilized bioreactor for alcoholic fermentation Pending JPS61185180A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2452885A JPS61185180A (en) 1985-02-13 1985-02-13 Immobilized bioreactor for alcoholic fermentation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2452885A JPS61185180A (en) 1985-02-13 1985-02-13 Immobilized bioreactor for alcoholic fermentation

Publications (1)

Publication Number Publication Date
JPS61185180A true JPS61185180A (en) 1986-08-18

Family

ID=12140650

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2452885A Pending JPS61185180A (en) 1985-02-13 1985-02-13 Immobilized bioreactor for alcoholic fermentation

Country Status (1)

Country Link
JP (1) JPS61185180A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0652500U (en) * 1990-12-12 1994-07-19 有限会社イズミ・エンタープライズ Yeast immobilization column using curved tube

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0652500U (en) * 1990-12-12 1994-07-19 有限会社イズミ・エンタープライズ Yeast immobilization column using curved tube

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