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JPS638753B2 - - Google Patents
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JPS638753B2 - - Google Patents

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Publication number
JPS638753B2
JPS638753B2 JP56166461A JP16646181A JPS638753B2 JP S638753 B2 JPS638753 B2 JP S638753B2 JP 56166461 A JP56166461 A JP 56166461A JP 16646181 A JP16646181 A JP 16646181A JP S638753 B2 JPS638753 B2 JP S638753B2
Authority
JP
Japan
Prior art keywords
fermentation
fermenter
tank
rate
liquid
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
JP56166461A
Other languages
Japanese (ja)
Other versions
JPS5871888A (en
Inventor
Toshibumi Ida
Toshiro Shimotokube
Tetsuo Maeda
Toshihiko Hirose
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.)
Toyo Engineering Corp
Original Assignee
Toyo Engineering 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 Toyo Engineering Corp filed Critical Toyo Engineering Corp
Priority to JP56166461A priority Critical patent/JPS5871888A/en
Publication of JPS5871888A publication Critical patent/JPS5871888A/en
Publication of JPS638753B2 publication Critical patent/JPS638753B2/ja
Granted legal-status Critical Current

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Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel

Landscapes

  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Description

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

この発明は、発酵反応熱と発酵生産物の蒸発潜
熱を回収し利用するエネルギー少消費型の、発酵
生産物の製造方法に関する。 最近、石油資源などの代替エネルギー源として
バイオマスが注目されており、例えば、バイオマ
スからガソリン添加用や各種燃料用のアルコール
を製造する発酵法の開発が期待されている。しか
し、従来のアルコール発酵プロセスは、投入エネ
ルギーと産出エネルギーの比が1に近く、エネル
ギー効率に問題があるので、バイオマスからの代
替エネルギーとしてのアルコールを製造する方法
としては適当とはいえなかつた。 すなわち、従来の発酵プロセスでは、発酵生
産物の生成濃度が低く、これを濃縮するには多大
のエネルギーを必要とする アルコール発酵の
場合、生成するアルコールが酵母の発酵阻害を起
こし、アルコールの生成速度を制約する 発酵
反応熱(例えばエタノール発酵では約13Kcal/
molエタノール)を除去するため多量の冷却水が
必要であり、その熱により昇温した冷却水はムダ
に廃棄されている さらにその冷却水の循環の
ための動力を要し、また作業環境も冷却水の飛散
などにより良くなく、構造物の腐食等も著しい、
という問題点があつた。 このような発酵プロセスを改良するものとし
て、これまでも種々の方法および装置が提案され
ている。 例えば、発酵槽から一部抜き出した液を熱交換
器で加熱後、フラツシユ蒸発器に導き、エタノー
ルに富む蒸気を気相に取り出し、これを精留塔に
導びいて共沸エタノールとし、さらにこの精留塔
塔頂蒸気をコンプレツサーで断熱圧縮して、精留
塔熱源、フラツシユ蒸発器の前段の熱交換器熱源
して利用する方法(ATPAL法、Chem.Age.
Nov.21、(1980)p11)がある。しかし、この方
法は、精留塔でエタノール蒸気を、全生成量と
還流に必要な量(平衡する水分を含めて)、蒸発
させなければならないので、精留塔蒸気のコンプ
レツサーの容量が、アルコール製造規模の割に膨
大になる コンプレツサーの出口ガスの一部を
精留塔のリボイラー熱源として利用しているの
で、アルコール収集タンクの温度が高くなり、ベ
ントからの、エタノールの蒸発による逃げが大き
くなる 発酵速度を大とするために、既に微生
物(菌体)の活動しうる最高温度で発酵を行つて
いる場合、発酵液を熱交換器でさらに加熱する
と、発酵液中の微生物に、熱的シヨツクを与え、
そのため活性を停止させ、取り返しのつかない損
傷を与えることがある、という欠点を有してい
る。 また、蒸発冷却器に発酵液を循環させ、発酵液
の一部である水を蒸発させ、菌体濃度と培養液濃
度が高められかつ冷却された発酵液を還流する方
式(特公昭39−26041号)がある。しかし、この
方式は、蒸発潜熱の回収、利用については何も行
つておらず、熱効率の点で満足できるものとは言
えなかつた。 発明者らは、こうした従来法の欠点および問題
点を克服するため種々検討を重ねた結果、発酵槽
を、発酵速度に応じて、発酵速度の大なる前発酵
槽と、発酵速度の小なる後発酵槽に分かち、第1
段の発酵速度の大なる発酵槽に減圧フラツシユ蒸
発槽を連結して発酵液をフラツシユ蒸発槽に循環
させ、自己蒸発によるフラツシユ蒸発を行つて、
発酵生産物蒸気の取り出しと、その蒸発潜熱によ
る発酵液の温度制御をはかり、所定割合の発酵を
完了した後、第1段階の発酵液を後発酵槽に送り
発酵を完結させるようにし、この第2段階の発酵
液を前記第1段階の発酵におけるフラツシユ槽か
らの蒸気により加熱することにより、発酵熱と発
酵生産物(平衡する水分を含む)の蒸発潜熱を有
効に利用して、冷却水を必要とせず、かつ極めて
エネルギー効率良く発酵を行うことができ、上記
目的に合致することを見出した。この発明は、こ
のような知見に基づきなされるに至つたものであ
る。 すなわちこの発明は、発酵槽を発酵反応速度に
応じて、反応速度の大なる前発酵槽と反応速度の
小なる後発酵槽の2段に分かち、前発酵槽におい
て、これと連結してフラツシユ蒸発槽を設け、前
発酵槽とフラツシユ蒸発槽間に発酵液を循環させ
ながら、フラツシユ蒸発を行うと共に反応速度の
大なる発酵を行わせ、次いでこの発酵を終えた発
酵液を後発酵槽に導入して発酵を完結させ、さら
にこの発酵を終えた熟成もろみを前記のフラツシ
ユ蒸発槽からの、平衡水分蒸気を含む発酵生産物
蒸気により加熱するようにしたことを特徴とする
発酵生産物の製造方法を提供するものである。 この発明方法においては、発酵槽を発酵速度に
応じて前後2段に分ける。なお前段、後段の発酵
槽は適宜複数の発酵槽から構成してもよい。この
場合発酵槽を2段に分けないで1段で全発酵を実
施すると、発酵速度の大きい発酵反応の時間より
も発酵速度の小さい発酵反応の時間が大きいため
発酵槽の容積効率(単位体積当りの発酵収量)が
悪くなる。また、発酵時の温度制御も、発酵速度
が大きい時の発熱量が大で、この時の発酵液の温
度制御が必要であるから、上記のように2段に分
離することにより温度制御が容易かつ効率的に実
施できる。この時、第2段の発酵は開放型の発酵
槽で、冷却水を必要としないで行うことができ
る。 この第1段階の前発酵槽の操作時間(槽内滞留
時間)は、一般的には、発酵速度がピークを過ぎ
て、このピークのA割まで低下するまでの時間で
ある。このAはフラツシユ発酵最適操作係数とい
うことができ、上述の前発酵槽の発酵操作の終り
における発酵生産物生成速度は次式で表わされ
る。 dc/dt=A(dc/dt)nax 但し、c:発酵生産物濃度 t:発酵時間 dc/dt:発酵生産物生成速度 (dc/dt)nax:最大発酵生産物生成速度 A:フラツシユ発酵最適操作係数 Aは、エタノール発酵の場合、0.05〜0.83好ま
しくは0.11〜0.56の範囲である。アセトン・ブタ
ノール発酵の場合Aは0.075〜0.14の範囲である。
Aがこれらの範囲を外れて大きすぎると、前段で
の熱回収が十分ではなく、しかも後段の発酵槽で
の温度上昇が5℃以上となる。またAが小さすぎ
ると後段の発酵槽の温度上昇が1℃以下と小さく
なる割に、前段の発酵槽容積が大きくなり、発酵
槽容積効率が悪くなる。 この発明では発酵速度の大なる第1段の発酵槽
には、フラツシユ蒸発槽を連結して設ける。これ
により発酵槽の除熱と温度の均一化が達成され
る。なお発酵槽とフラツシユ蒸発槽間の発酵液の
循環は、両者の槽内の操作圧力差を利用して行う
ことができる。フラツシユ蒸発槽の能力は発酵反
応熱を除去するのに十分な大きさのものとし、フ
ラツシユ蒸発槽への発酵液循環流量は発酵速度す
なわち発酵反応熱に相当した量で設定される。こ
の際、循環流量のコントロールはフラツシユ蒸発
槽の液面を一定になるようにして行う。 なお発酵槽を回分式操作とする場合は、複数個
の発酵槽に相当数のフラツシユ蒸発槽を組み合わ
せ、一定時間間隔の時差並列で運転することによ
り、回分式発酵槽から発生する蒸気の流量変動を
並列の数の分だけ均一化するのが好ましい。 フラツシユ蒸発槽で発生させた発酵生成物を含
む蒸気は、回収後、蒸気のもつ発酵熱エネルギー
を蒸留工程で利用しやすい形に変換される。これ
は、フラツシユ蒸発槽の真空度を達成し、蒸気を
抜き出す真空ポンプを2段階に分けて設置し、第
1段階の真空ポンプを出た蒸気を第2段階の真空
ポンプに入る前に後発酵槽からの熱成もろみで冷
却して凝縮させると同時に発酵液を予熱すること
によつて行うのが好ましい。 次に図面に基づき、この発明の方法をさらに詳
細に説明する。 図面はこの発明の方法の1実施態様を簡略化し
て示すフローシートであり、酵母によるエタノー
ル発酵の例である。 前発酵槽2は、5基の発酵タンクからなり、そ
れぞれに、所定量の発酵液を発酵液供給ライン1
9から仕込んでいく。次いで酒母槽1より、あら
かじめ培養しておいた酒母を前発酵槽2に添加
し、空気ライン20より空気を吹き込み、発酵を
開始させる。21は炭酸ガスに同伴するエタノー
ル蒸気を回収するスクラバーである。酒母添加後
数時間経過後、発酵液を前発酵槽2から一部抜き
出し、これを、循環ポンプ3を有する液循環ライ
ン4によつて前記の5基の発酵タンクにそれぞれ
連結させた5基のフラツシユドラムからなるフラ
ツシユ蒸発槽との間を循環させる。フラツシユ蒸
発槽5において減圧下でエタノールを蒸発させた
発酵液は前発酵槽2へ返される。このようにして
一定割合の発酵を終えた後、前発酵槽2の発酵液
は、取り出しライン15から取り出されて後発酵
槽6に送り込まれ、所定時間滞留させて残りの発
酵、熟成が行われる。 フラツシユ蒸発槽5から発生した蒸気は、ヘツ
ダーに集められた後、真空ポンプ17を設けた蒸
気ライン8の真空ポンプ17で圧縮後、中間冷却
器9に通される。そしてここで、後発酵槽6から
抜き出され、もろみ液ライン16をポンプ7によ
つて送られてきた熟成もろみとの熱交換が行われ
る。蒸気はこれにより冷却されて凝縮し、凝縮液
は気液分離器10で分離される。凝縮しなかつた
蒸気は真空ポンプ12を有するライン11に送ら
れ、真空ポンプ12で再圧縮後、最終冷却器13
で冷却凝縮させられる。上記気液分離器10から
の凝縮液はライン14から、熟成もろみ槽18に
送られ、冷却器13からの凝縮液も熟成もろみ槽
18に送り込まれ、これらの凝縮液は顕熱により
昇温しているので、この熟成もろみ槽18にもろ
み液ライン16から送り込まれる熟成もろみと混
合されることにより、熟成もろみをさらに昇温さ
せる。このようにして加温された熟成もろみはラ
イン22より、蒸留工程に送られる。 上記において操作条件としては、前発酵槽2の
温度は28〜35℃が好ましい。この範囲を外れて温
度が低すぎたり、高すぎたりすると、発酵歩合が
低下する。またその圧力は1気圧が発生した炭酸
ガスを大気放散する上で好ましい。 また後発酵槽6の温度は前発酵槽2の温度より
2℃以上高くない範囲、すなわち35〜37℃以下で
あり、圧力は1気圧で行うことができる。 フラツシユ蒸発槽5の温度は前発酵槽2より0
〜2℃低くするのが好ましく、その時の発酵液の
沸とう圧力が操作圧力となり、通常25〜70Torr
である。 次に、気液分離器10は、後発酵槽6からの熟
成もろみ液で冷却可能とするため、熟成もろみ液
温+3℃以上の温度で平衡な圧力、すなわち60〜
500Torr、好ましくは100〜250Torrとする。 なお、上記説明では前発酵槽を回分式で操作す
る場合について述べたが、これに限定されず適宜
連続式を採用できることはいうまでもない。 次表に上述のフローシートの方法に従がうエタ
ノール生産規模100K/Dayの発酵装置を用い
て発酵を行つた場合のユーテイリテイ消費量、発
酵槽容積効率などを、従来法と比較して示す。
The present invention relates to a method for producing fermented products that consumes less energy and that recovers and utilizes the fermentation reaction heat and the latent heat of vaporization of the fermented products. Recently, biomass has been attracting attention as an alternative energy source to petroleum resources, and there are expectations for the development of fermentation methods for producing alcohol for use in gasoline additives and various fuels from biomass, for example. However, in the conventional alcohol fermentation process, the ratio of input energy to output energy is close to 1, and there is a problem in energy efficiency, so it cannot be said to be suitable as a method for producing alcohol as an alternative energy source from biomass. In other words, in conventional fermentation processes, the concentration of fermentation products produced is low, and a large amount of energy is required to concentrate them.In the case of alcoholic fermentation, the alcohol produced inhibits yeast fermentation, reducing the rate of alcohol production. Fermentation reaction heat (for example, in ethanol fermentation, about 13 Kcal/
mol ethanol), a large amount of cooling water is required, and the cooling water that has heated up due to the heat is wasted.Moreover, power is required to circulate the cooling water, and the work environment is also cooled. It is not good due to water splashing, etc., and there is also significant corrosion of the structure.
There was a problem. Various methods and devices have been proposed to improve such fermentation processes. For example, a portion of the liquid extracted from the fermenter is heated in a heat exchanger, then guided to a flash evaporator, the ethanol-rich vapor is extracted into the gas phase, and this is led to a rectification column to produce azeotropic ethanol. A method in which the vapor at the top of the rectifying column is adiabatically compressed using a compressor and used as a heat source for the rectifying column and a heat exchanger in the front stage of the flash evaporator (ATPAL method, Chem.Age.
Nov. 21, (1980) p11). However, in this method, the rectifier must evaporate the ethanol vapor in the amount required for the total production and reflux (including water to balance), so the capacity of the rectifier vapor compressor is The volume is huge considering the scale of production.A portion of the compressor outlet gas is used as a reboiler heat source for the rectification column, which increases the temperature of the alcohol collection tank and increases the amount of ethanol that escapes from the vent due to evaporation. In order to increase the fermentation rate, if fermentation is already carried out at the maximum temperature at which microorganisms (bacterial cells) can be active, further heating the fermentation liquid with a heat exchanger will cause a thermal shock to the microorganisms in the fermentation liquid. give,
Therefore, it has the disadvantage that it may stop its activity and cause irreversible damage. Another method is to circulate the fermentation liquid through an evaporative cooler, evaporate water that is part of the fermentation liquid, increase the bacterial cell concentration and culture liquid concentration, and recirculate the cooled fermentation liquid (Special Publication No. 39-26041 No.). However, this method did nothing to recover or utilize the latent heat of vaporization, and could not be said to be satisfactory in terms of thermal efficiency. As a result of various studies to overcome the shortcomings and problems of the conventional methods, the inventors have determined that the fermenters can be divided into two types, depending on the fermentation rate: a pre-fermenter with a high fermentation rate, and a post-fermenter with a low fermentation rate. Divided into fermenters, 1st
A reduced pressure flash evaporator is connected to the fermenter with a high fermentation rate in the stage, and the fermented liquid is circulated through the flash evaporator to perform flash evaporation by self-evaporation.
After the fermentation product vapor is taken out and the temperature of the fermented liquor is controlled by its latent heat of vaporization, and a predetermined proportion of fermentation is completed, the fermented liquor from the first stage is sent to the post-fermentation tank to complete the fermentation. By heating the fermentation liquid in the two stages with steam from the flashing tank in the first stage fermentation, the fermentation heat and the latent heat of vaporization of the fermentation product (including the equilibrium water) are effectively used to cool the cooling water. It has been found that fermentation can be carried out in an extremely energy-efficient manner without the need for this method, thus meeting the above objectives. This invention has been made based on such knowledge. That is, this invention divides the fermenter into two stages according to the fermentation reaction rate: a pre-fermenter with a high reaction rate and a post-fermenter with a low reaction rate, and connects the pre-fermenter with the post-fermenter to perform flash evaporation. A tank is provided, and the fermentation liquid is circulated between the pre-fermentation tank and the flash evaporation tank to carry out flash evaporation and fermentation with a high reaction rate, and then the fermented liquid that has completed this fermentation is introduced into the post-fermentation tank. A method for producing a fermented product, characterized in that the fermented mash is further heated by the fermented product vapor containing equilibrium moisture vapor from the above-mentioned flash evaporator. This is what we provide. In this invention method, the fermenter is divided into two stages, front and rear, depending on the fermentation speed. Note that the first stage and second stage fermenters may be composed of a plurality of fermenters as appropriate. In this case, if the entire fermentation is carried out in one stage without dividing the fermenter into two stages, the time for the fermentation reaction with a low fermentation rate is longer than the time for the fermentation reaction with a high fermentation rate, so the volumetric efficiency of the fermenter (per unit volume) (fermentation yield) deteriorates. In addition, temperature control during fermentation also requires temperature control of the fermentation liquid at this time, as the amount of heat generated is large when the fermentation rate is high, so temperature control is facilitated by separating it into two stages as described above. and can be implemented efficiently. At this time, the second stage fermentation can be carried out in an open fermenter without the need for cooling water. The operating time (residence time in the tank) of the pre-fermenter in this first stage is generally the time from when the fermentation rate passes the peak to when it drops to A percent of this peak. This A can be said to be the optimum operation coefficient for flash fermentation, and the fermentation product production rate at the end of the fermentation operation in the above-mentioned pre-fermenter is expressed by the following equation. dc/dt=A (dc/dt) nax , where c: fermentation product concentration t: fermentation time dc/dt: fermentation product production rate (dc/dt) nax : maximum fermentation product production rate A: optimum for flash fermentation The operating coefficient A ranges from 0.05 to 0.83, preferably from 0.11 to 0.56, in the case of ethanol fermentation. In the case of acetone-butanol fermentation, A ranges from 0.075 to 0.14.
If A is too large outside these ranges, heat recovery in the first stage will not be sufficient and the temperature increase in the second stage fermenter will be 5° C. or more. On the other hand, if A is too small, the volume of the fermenter at the front stage becomes large even though the temperature rise in the fermenter at the later stage is as small as 1° C. or less, and the volumetric efficiency of the fermenter deteriorates. In this invention, a flash evaporation tank is connected to the first stage fermenter having a high fermentation rate. This achieves heat removal and temperature uniformity from the fermenter. Note that the fermentation liquid can be circulated between the fermentation tank and the flash evaporation tank by utilizing the operating pressure difference in the two tanks. The capacity of the flash evaporator is set to be large enough to remove the heat of fermentation reaction, and the flow rate of the fermentation liquor circulated to the flash evaporator is set at an amount corresponding to the fermentation rate, that is, the heat of fermentation reaction. At this time, the circulation flow rate is controlled so that the liquid level in the flash evaporation tank remains constant. If the fermenter is operated in batch mode, multiple fermenters are combined with a considerable number of flash evaporators and operated in parallel at fixed time intervals to reduce fluctuations in the flow rate of steam generated from the batch fermenter. It is preferable to equalize by the number of parallel lines. After the steam containing the fermentation products generated in the flash evaporator is recovered, the fermentation heat energy contained in the steam is converted into a form that can be easily used in the distillation process. This is achieved by installing vacuum pumps in two stages to achieve the vacuum level in the flash evaporation tank and extracting steam, and then post-fermenting the steam leaving the first stage vacuum pump before entering the second stage vacuum pump. Preferably, this is carried out by cooling and condensing the thermal mash from the tank and at the same time preheating the fermentation liquor. Next, the method of the present invention will be explained in more detail based on the drawings. The drawing is a flow sheet showing a simplified embodiment of the method of the present invention, and is an example of ethanol fermentation using yeast. The pre-fermentation tank 2 consists of five fermentation tanks, each of which receives a predetermined amount of fermentation liquid through the fermentation liquid supply line 1.
Start preparing from 9. Next, a pre-cultured yeast mash is added to the pre-fermentation tank 2 from the mash tank 1, and air is blown through the air line 20 to start fermentation. 21 is a scrubber that recovers ethanol vapor accompanying carbon dioxide gas. After several hours have passed after addition of the yeast mash, a portion of the fermentation liquid is extracted from the pre-fermentation tank 2 and transferred to the five fermentation tanks each connected to the above-mentioned five fermentation tanks by a liquid circulation line 4 having a circulation pump 3. It is circulated between a flash evaporation tank consisting of a flash drum. The fermented liquid from which ethanol has been evaporated under reduced pressure in the flash evaporator 5 is returned to the pre-fermenter 2. After a certain percentage of fermentation has been completed in this way, the fermented liquor in the pre-fermenter 2 is taken out from the take-out line 15 and sent to the post-fermenter 6, where it is allowed to stay for a predetermined period of time to perform the remaining fermentation and aging. . The steam generated from the flash evaporation tank 5 is collected in a header, compressed by a vacuum pump 17 in a steam line 8 provided with a vacuum pump 17, and then passed through an intercooler 9. Here, heat exchange is performed with the aged mash extracted from the post-fermentation tank 6 and sent through the mash line 16 by the pump 7. The vapor is thereby cooled and condensed, and the condensed liquid is separated in the gas-liquid separator 10. The uncondensed vapor is sent to a line 11 with a vacuum pump 12, and after being recompressed by the vacuum pump 12, it is sent to a final cooler 13.
It is cooled and condensed. The condensed liquid from the gas-liquid separator 10 is sent from the line 14 to the aging mash tank 18, and the condensed liquid from the cooler 13 is also sent to the aged mash tank 18, and these condensed liquids are heated by sensible heat. Therefore, the temperature of the aged mash is further raised by mixing it with the aged mash fed into the aged mash tank 18 from the mash liquid line 16. The aged mash heated in this way is sent to the distillation process via line 22. In the above operation conditions, the temperature of the pre-fermenter 2 is preferably 28 to 35°C. If the temperature is too low or too high outside this range, the fermentation rate will decrease. Further, the pressure is preferably 1 atm in order to diffuse the generated carbon dioxide into the atmosphere. Further, the temperature of the post-fermenting tank 6 is within a range not higher than the temperature of the pre-fermenting tank 2 by 2°C or more, that is, 35-37°C or less, and the pressure can be 1 atm. The temperature of the flash evaporator 5 is lower than that of the pre-fermenter 2.
It is preferable to lower the temperature by ~2℃, and the boiling pressure of the fermented liquid at that time becomes the operating pressure, which is usually 25 to 70 Torr.
It is. Next, in order to enable the gas-liquid separator 10 to be cooled with the matured mash from the post-fermenter 6, the pressure is maintained at equilibrium at a temperature of 3°C or higher, i.e., 60~60°C.
500 Torr, preferably 100 to 250 Torr. In the above description, a case has been described in which the pre-fermenter is operated in a batch manner, but it goes without saying that the method is not limited to this and a continuous type can be employed as appropriate. The following table shows the utility consumption, fermenter volumetric efficiency, etc. when fermentation is carried out using a fermentation device with an ethanol production scale of 100K/day according to the method in the above flow sheet, in comparison with the conventional method.

【表】【table】

【表】 ただし、従来法は、この発明の方法に対し、発
酵槽槽壁の潅液冷却による温度管理方式を採用
し、したがつてフラツシユ蒸発槽も蒸気圧縮装置
もなく、前段、後段に分割した発酵システムを採
用していない点が異なるものである。 以上のように、この発明は、発酵槽を前後2段
に分け、発酵生成物の蒸発潜熱の利用と発酵反応
熱の回収をはかるものであり、下記のような優れ
た作用効果を奏する。 (1) 従来回収されていなかつた発酵反応熱を回収
して、発酵を完了した熟成もろみ液の予熱に利
用できるので例えば、蒸留工程のような後続工
程の熱エネルギーを非常に節減でき、エネルギ
ー少消費型の発酵生産物の製造方法として好適
である。 (2) 発酵槽の水冷が不要となり、冷却装置、冷却
水が不要となる。したがつて、冷却水循環用の
所要動力も軽減される。 (3) 発酵生産物を前発酵槽から一定量除去しなが
ら発酵を行うので、発酵生産物の発酵阻害を防
止でき、発酵反応速度を高めて、生産量を増大
させることができる。発酵生成物が溶剤(水な
ど)に対する比揮発度が1以上の場合、特に仕
込濃度を従来より大きく出来る。 この発明方法は、エタノール発酵、アセトン・
ブタノール発酵など発酵生産物がその発酵温度で
蒸気圧を有する揮発性物質である発熱発酵反応に
対して適用することができる。 次にこの発明を実施例に基づきさらに詳細に説
明する。なお説明中の%は重量%を表わす。 実施例 図面に示したこの発明のフローシートに従がい
エタノール発酵を行つた。 発酵液供給ライン19から、前発酵槽2の各タ
ンクに12時間おきに時間をずらして、糖液15.3
%、水82.2%、その他栄養分2.5%からなる発酵
液を、45390Kg/hrで仕込んでゆき、各タンクに
発酵液をそれぞれ554680Kg仕込んだ。仕込み完了
後各タンクに酒母を添加し、最初数時間のみ空気
ライン20より空気を吹き込み、前発酵槽2の発
酵を33℃1気圧で開始させた。酒母添加5時間
後、前発酵槽2から、発酵液を199720Kg/hrで抜
き出し、フラツシユ蒸発槽5との間の循環を開始
させる。フラツシユ蒸発槽5は33℃64Torrで操
作する。このようにして発酵を行わせ、発酵開始
後48時間後前発酵槽2の発酵液の組成はエタノー
ル7.0%、糖液1.8%、水88.5%、その他3.0%とな
つた。そこで、この発酵液を40720Kg/hrで取り
出しライン15から取り出し、後発酵槽6に導入
した。この後発酵槽6では発酵液をそのまま1気
圧で72時間滞留させて残りの発酵、熟成を行い、
エタノール7.6%、水87.4%、その他2.93%の組成
で35.4℃の熟成もろみを得た。 一方、フラツシユ蒸発槽5から発生し、ヘツダ
ーに集められた蒸気は、エタノール19.2%、
CO20.9%、水79.9%の組成を有し1590Kg/hrの発
生量であつた。このエタノール蒸気を真空ポンプ
17で圧縮して285℃250Torrの蒸気とした後、
中間冷却器9に導き、ここで、前記の、後発酵槽
6から抜き出され、もろみ液ライン16から送ら
れてきた、熟成もろみ40290Kg/hr(35.4℃)との
熱交換が行われ、熟成もろみは57℃にまで加熱さ
れる。一方エタノール蒸気はこの結果冷却されて
凝縮し、50℃200Torrの混相流となり、凝縮液は
気液分離器10で分離された。凝縮液は組成エタ
ノール18.2%、水81.8%、温度50℃であり、1540
Kg/hrで熟成もろみ槽18に送られる。気液分離
器10で凝縮しなかつた蒸気は真空ポンプ12で
再圧縮後、最終冷却器13で冷却されて、エタノ
ール62.3%、水37.7%の凝縮液を40Kg/hrで生成
し、熟成もろみ槽18に送り込まれる。これらの
凝縮液は、もろみ液ライン16から、この熟成も
ろみ槽18に送り込まれた前記の57℃に昇温した
熟成もろみと混合されて、エタノール8.0%、水
89.1%、その他2.8%の組成で温度56.7℃の熟成も
ろみが41860Kg/hrで得られた。
[Table] However, in contrast to the method of the present invention, the conventional method adopts a temperature control method by cooling the fermenter tank wall with irrigation water, and therefore does not have a flash evaporator or vapor compression device, and is divided into a front stage and a rear stage. The difference is that it does not use a traditional fermentation system. As described above, the present invention divides the fermenter into two stages, front and rear, and utilizes the latent heat of vaporization of the fermented product and recovers the heat of fermentation reaction, and achieves the following excellent effects. (1) Fermentation reaction heat, which has not been recovered in the past, can be recovered and used to preheat the aged mash after fermentation, which greatly reduces thermal energy in subsequent processes such as the distillation process. This method is suitable as a method for producing consumable fermentation products. (2) There is no need to water-cool the fermenter, so there is no need for a cooling device or cooling water. Therefore, the power required for circulating the cooling water is also reduced. (3) Since fermentation is carried out while removing a certain amount of fermentation products from the pre-fermentation tank, it is possible to prevent fermentation inhibition of the fermentation products, increase the fermentation reaction rate, and increase the production amount. When the fermentation product has a relative volatility of 1 or more with respect to a solvent (such as water), the concentration of the fermentation product can be increased compared to the conventional method. This invention method includes ethanol fermentation, acetone fermentation,
It can be applied to exothermic fermentation reactions, such as butanol fermentation, where the fermentation product is a volatile substance that has a vapor pressure at its fermentation temperature. Next, the present invention will be explained in more detail based on examples. Note that % in the description represents weight %. EXAMPLE Ethanol fermentation was carried out according to the flow sheet of the present invention shown in the drawings. From the fermentation solution supply line 19 to each tank of the pre-fermentation tank 2, 15.3% of the sugar solution is supplied at staggered intervals of 12 hours.
%, water 82.2%, and other nutrients 2.5% was charged at a rate of 45390 kg/hr, and each tank was charged with 554680 kg of fermented liquid. After the preparation was completed, the mash was added to each tank, air was blown through the air line 20 for the first few hours, and fermentation in the pre-fermentation tank 2 was started at 33°C and 1 atm. After 5 hours of addition of the yeast mother, the fermentation liquor is extracted from the pre-fermentation tank 2 at a rate of 199,720 kg/hr, and circulation with the flash evaporation tank 5 is started. The flash evaporator 5 is operated at 33° C. and 64 Torr. Fermentation was carried out in this manner, and 48 hours after the start of fermentation, the composition of the fermentation liquor in the pre-fermenter 2 was 7.0% ethanol, 1.8% sugar solution, 88.5% water, and 3.0% others. Therefore, this fermentation liquid was taken out from the takeout line 15 at a rate of 40,720 kg/hr and introduced into the post-fermentation tank 6. After this, in the fermentation tank 6, the fermented liquid is left as it is at 1 atm for 72 hours to carry out the remaining fermentation and aging.
A matured mash at 35.4°C was obtained with a composition of 7.6% ethanol, 87.4% water, and 2.93% others. On the other hand, the steam generated from the flash evaporation tank 5 and collected in the header contains 19.2% ethanol,
The composition was 0.9% CO 2 and 79.9% water, and the amount generated was 1590 Kg/hr. After compressing this ethanol vapor with the vacuum pump 17 to make it into vapor at 285°C and 250 Torr,
It is led to the intercooler 9, where it undergoes heat exchange with the aged mash (40,290 kg/hr (35.4°C)) extracted from the post-fermenter 6 and sent from the mash liquid line 16, and aged. The moromi is heated to 57℃. On the other hand, the ethanol vapor was cooled and condensed to form a multiphase flow at 50° C. and 200 Torr, and the condensed liquid was separated in the gas-liquid separator 10. The condensate has a composition of 18.2% ethanol, 81.8% water, and a temperature of 50℃.
Kg/hr is sent to aging mash tank 18. The vapor that is not condensed in the gas-liquid separator 10 is recompressed in the vacuum pump 12 and then cooled in the final cooler 13 to produce a condensate containing 62.3% ethanol and 37.7% water at a rate of 40 kg/hr. Sent to 18. These condensates are mixed with the aged mash, which has been heated to 57°C, which is sent from the mash line 16 to the aged mash tank 18, and is mixed with 8.0% ethanol and water.
Aged mash with a composition of 89.1% and 2.8% at a temperature of 56.7°C was obtained at a rate of 41,860 Kg/hr.

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

図面はこの発明の発酵生産物の製造方法の1例
を示すフローシートである。 符号の説明、2……前発酵槽、4……液循環ラ
イン、5……フラツシユ蒸発槽、6……後発酵
槽、8……発生蒸気ライン、9……中間冷却器、
10……気液分離器、12,17……真空ポン
プ、14……凝縮液ライン、16……もろみ液ラ
イン、18……熟成もろみ槽、19……原料液供
給ライン、20……空気ライン、22……熟成も
ろみ取り出しライン。
The drawing is a flow sheet showing one example of the method for producing fermented products of the present invention. Explanation of symbols, 2... Pre-fermenter, 4... Liquid circulation line, 5... Flush evaporator, 6... Post-fermenter, 8... Generated steam line, 9... Intercooler,
10... Gas-liquid separator, 12, 17... Vacuum pump, 14... Condensate line, 16... Mash liquid line, 18... Aging mash tank, 19... Raw material liquid supply line, 20... Air line , 22... Aging mash removal line.

Claims (1)

【特許請求の範囲】 1 発酵槽を発酵反応速度に応じて、反応速度の
大なる前発酵槽と反応速度の小なる後発酵槽の2
段に分かち、前発酵槽において、これと連結して
フラツシユ蒸発槽を設け、前発酵槽とフラツシユ
蒸発槽間に発酵液を循環させながら、フラツシユ
蒸発を行うと共に反応速度の大なる発酵を行わ
せ、次いでこの発酵を終えた発酵液を後発酵槽に
導入して発酵を完結させ、さらにこの発酵を終え
た熟成もろみを前記のフラツシユ蒸発槽からの、
平衡水分蒸気を含む発酵生産物蒸気により加熱す
るようにしたことを特徴とする発酵生産物の製造
方法。 2 発酵反応が、エタノール発酵又はアセトン・
ブタノール発酵であり、前発酵槽における発酵操
作を、発酵生産物生成速度がピークを過ぎ dc/dt=A(dc/dt)nax (但し、c:発酵生産物濃度 t:発酵時間 dc/dt:発酵生産物生成速度 (dc/dt)nax:最大発酵生産物生成速度 であり、Aは0.05〜0.83(エタノール発酵の場合
は0.05〜0.83、アセトン・ブタノール発酵の場合
は0.075〜0.14)である。)で規定される範囲に達
するまで行う特許請求の範囲第1項記載の発酵生
産物の製造方法。 3 平衡水分蒸気を含む発酵生産物蒸気により加
熱した熟成もろみを蒸留工程に送る特許請求の範
囲第1項記載の発酵生産物の製造方法。
[Scope of Claims] 1. Fermentation tanks are divided into two types according to the fermentation reaction rate: a pre-fermenter with a high reaction rate and a post-fermenter with a low reaction rate.
The pre-fermenter is divided into stages, and a flash evaporation tank is connected to the pre-fermenter, and the fermentation liquid is circulated between the pre-fermenter and the flash evaporator to perform flash evaporation and fermentation with a high reaction rate. Then, the fermented liquor that has completed this fermentation is introduced into the post-fermentation tank to complete the fermentation, and the aged mash that has completed this fermentation is then transferred from the above-mentioned flat evaporation tank.
A method for producing a fermented product, characterized in that heating is performed using fermented product vapor containing equilibrium water vapor. 2 The fermentation reaction is ethanol fermentation or acetone fermentation.
This is butanol fermentation, and the fermentation operation in the pre-fermenter is performed until the fermentation product production rate has passed the peak dc/dt = A (dc/dt) nax (where c: fermentation product concentration t: fermentation time dc/dt: Fermentation product production rate (dc/dt) nax : Maximum fermentation product production rate, A is 0.05 to 0.83 (0.05 to 0.83 in the case of ethanol fermentation, 0.075 to 0.14 in the case of acetone/butanol fermentation). ) The method for producing a fermented product according to claim 1, wherein the method is carried out until the range specified in (1) is reached. 3. The method for producing a fermented product according to claim 1, wherein the aged mash heated by fermented product vapor containing equilibrium water vapor is sent to a distillation process.
JP56166461A 1981-10-20 1981-10-20 Method for producing fermented products Granted JPS5871888A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56166461A JPS5871888A (en) 1981-10-20 1981-10-20 Method for producing fermented products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56166461A JPS5871888A (en) 1981-10-20 1981-10-20 Method for producing fermented products

Publications (2)

Publication Number Publication Date
JPS5871888A JPS5871888A (en) 1983-04-28
JPS638753B2 true JPS638753B2 (en) 1988-02-24

Family

ID=15831824

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56166461A Granted JPS5871888A (en) 1981-10-20 1981-10-20 Method for producing fermented products

Country Status (1)

Country Link
JP (1) JPS5871888A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2405830C2 (en) * 2009-02-18 2010-12-10 Дэвон Инвестмент Лимитед Method of preparing organic solvents

Also Published As

Publication number Publication date
JPS5871888A (en) 1983-04-28

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