JPS6338191B2 - - Google Patents
Info
- Publication number
- JPS6338191B2 JPS6338191B2 JP56150673A JP15067381A JPS6338191B2 JP S6338191 B2 JPS6338191 B2 JP S6338191B2 JP 56150673 A JP56150673 A JP 56150673A JP 15067381 A JP15067381 A JP 15067381A JP S6338191 B2 JPS6338191 B2 JP S6338191B2
- Authority
- JP
- Japan
- Prior art keywords
- fermentation
- evaporator
- heat exchanger
- vapor
- built
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M21/00—Bioreactors or fermenters specially adapted for specific uses
- C12M21/12—Bioreactors or fermenters specially adapted for specific uses for producing fuels or solvents
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M29/00—Means for introduction, extraction or recirculation of materials, e.g. pumps
- C12M29/02—Percolation
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M43/00—Combinations of bioreactors or fermenters with other apparatus
- C12M43/02—Bioreactors or fermenters combined with devices for liquid fuel extraction; Biorefineries
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS 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
- C12M47/00—Means for after-treatment of the produced biomass or of the fermentation or metabolic products, e.g. storage of biomass
- C12M47/10—Separation or concentration of fermentation products
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Sustainable Development (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Description
この発明は発酵液の熱エネルギーを有効に利用
したエタノール、アセトン、ブタノールなどの発
酵生産物の製造方法に関する。
微生物を利用した発酵プロセスは、従来盛んに
行われてきた化学合成法に比べ、常温常圧付近で
合成反応が行える利点があるが、一般に目的の生
産物の生成濃度が低く(エタノール発酵で10%
位、アセトンブタノール発酵で1〜2%など)、
そのためこれを濃縮分離するには多大のエネルギ
ーを消費するという欠点がある。
しかるに一方では、発酵反応に伴い微生物から
発生する熱、すなわち反応熱は、通常、シヤワー
クーラー、フラツシユクーラー、冷却コイルなど
でただ除去しているのが現状である。この発生す
る熱は、エタノール発酵では次式のように
26Kcal/molグルコースに達する。これは、例え
ば10%エタノール水溶液からエタノールをストリ
ツプさせるのに必要な熱量の約1/4に達する。
C6H12O6→2C2H5OH+CO2
+26Kcal/molグルコース
この発酵プロセスの欠点を改良するためにこれ
まで種々の方法及び装置が提案されている。例え
ば、エタノールの発酵生産に際して発酵槽、な
いしは発酵槽と組み合せたフラツシユ槽を減圧し
てエタノールに富む蒸発を取り出す方法(米国特
許第2440925号)、発酵生産による発熱を、減圧
蒸発冷却器に発酵液を循環させることにより除去
する方式(特公昭39−26041号)がある。しかし
の方法は取り出した蒸気は、コンデンサーで冷
却しており、やはり熱をロスしている。また冷却
の際に常圧まで圧縮する動力が必要であり、コン
デンサーの冷却には深冷が必要などの問題点があ
る。またの方式は発酵液の濃縮を意図してお
り、発酵反応発熱量に見合う分の揮発性発酵生産
物(+水)しか得られないという欠点がある。
さらに、これらの従来技術についてエタノール
などの発酵生産物のもつエネルギーよりも、その
発酵生産物の生産に要するエネルギーの方が大き
いのではないかという厳しい論議もなされてい
る。そこで、特に低コスト・エタノール発酵法と
して、発酵槽から一部抜き出した液を熱交換器
を通して加熱後、減圧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
減圧精留塔に導いて共沸エタノール(95vol%
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、減
圧フラツシユ蒸発器の前段の熱交換器熱源として
利用する方法(ATPAL法、Chem.Age、
Nov.21、(1980)p11)が提案されている。しか
し、この方法では、エタノールを蒸発させるため
の熱量を顕熱の形で熱交換器から減圧フラツシユ
蒸発器まで運ぶために、循環発酵液量が大とな
り、熱交換器の必要伝熱面積も大となる欠点を有
していた。さらに、この方法の欠点として、発酵
槽での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
中の菌体に、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起こすこ
とがある。
発明者らは、こうした従来法の欠点及び問題点
を克服するため種々検討を重ねた結果、発酵生産
物を含有する発酵液を発酵槽より一部抜き出し、
これを、発酵温度での蒸気圧以下に減圧した熱交
換器内蔵蒸発器に導き、揮発性の(水より沸点の
低い)発酵生産物を蒸発させ、この発酵生産物を
含む蒸気を圧縮昇温して熱交換器内蔵蒸発器の加
熱源とすれば、上記の目的すなわち、発酵反応
熱の除去とその反応熱の蒸発への有効利用及び
省エネルギー的で菌体を損傷させない発酵生産物
の蒸発濃縮が達成できることを見出した。この発
明はこの知見に基づいて完成されるに至つたもの
である。
すなわちこの発明は、発酵槽より、揮発性の発
酵生産物を含有する発酵液の一部を抜き出し、こ
れを、発酵温度での蒸気圧以下に減圧した液静水
頭が実質的に発生しない熱交換器内蔵蒸発器に循
環して、揮発性の発酵生産物の蒸気を発生させ、
この蒸気を断熱圧縮して昇温させて、その熱交換
器内蔵蒸発器の加熱源として利用することを特徴
とする揮発性発酵生産物の製造法を提供するもの
である。
この発明において、用いられる熱交換器内蔵蒸
発器の方式としては特に制限はないが、熱交換器
が流下膜式、流下薄膜式、薄膜式(水平管型)、
Luwa型のような液静水頭が実質的に発生しない
構造のものが発酵液の冷却効率が良く、用いられ
る。
熱交換器内蔵蒸発器は、発酵温度での蒸気圧以
下に減圧して(揮発性の発酵生産物を含む発酵液
が発酵温度以下で沸騰する減圧度)で運転され
る。具体的な減圧度は、発酵反応の種類とその時
の発酵槽の発酵温度などによつて異なるが通常
720〜20torr、好ましくは150〜30torrの範囲であ
る。これをさらに具体的にいえばエタノール発酵
では、現在の酵母(Saccharomyces属)では常
圧で35℃程度が実用的に発酵を行い得る最高温度
であるが、エタノール濃度が6容量%で50torrま
で減圧するのが好ましい。
なお、発酵温度つまり発酵槽中の発酵液の温度
は発酵反応の種類によつて異なるが、通常20〜80
℃の範囲であり、好ましくは30〜65℃の範囲であ
る。
この発明において、発酵槽よりの発酵液の抜き
出し速度は発酵槽に滞留している発酵液の10%/
毎時〜180%/毎時の範囲が好ましい。
熱交換器内蔵蒸発器で揮発性の発酵生産物を蒸
発除去された発酵液は、その蒸発により発酵熱の
除去も行われた後、発酵槽に循環される。したが
つて発酵槽の冷却による発酵反応の円滑な進行
と、発酵生産物の除去による、発酵阻害の減少を
達成することができる。
一方、熱交換器内蔵蒸発器で蒸発除去された揮
発性の発酵生産物に富む蒸気は、断熱的に圧縮さ
れ、温度、圧力を上昇させられた後、前記熱交換
器内蔵蒸発器の加熱源として使用されて、自ら
は、その蒸発器中で冷却されて液化する。断熱圧
縮後の、揮発性の発酵生産物に富む蒸気は発酵槽
中の発酵液の温度より3〜20℃昇温している。
この発明の方法は、エタノール発酵、アセトン
ブタノール発酵などに適用することができる。
次に図面を参照しながらこの発明をさらに詳し
く説明する。第1図は、前記の従来法のATPAL
プロセスのフローシートを示し、第2図は本発明
方法の1実施態様としてのフローシートを示す。
第1図において、発酵槽1にフイードライン2
を通じて発酵原料が供給され、発酵反応により発
酵生産物が生産され、ガス状の生産物(例えば
CO2)はベントライン3を通じて排出される。揮
発性生産物を含む発酵液は、発酵液抜き出しライ
ン4を通じて抜き出され、熱交換器5で加熱され
た後、フラツシユ蒸発器6に送られ、フラツシユ
蒸発処理に付される。このフラツシユ蒸発により
分離された揮発性生産物に富む蒸気はライン7よ
り精留塔8に送られ、揮発性生産物の蒸気は精留
塔頂蒸気ライン9より蒸気圧縮機10に送られ、
この圧縮蒸気はライン11を経て、熱交換器5に
送られその加熱源として使用された後、ライン1
2より凝縮蒸気として取り出される。一方、揮発
性生産物に富む蒸気を放出した発酵液は発酵液戻
りライン13より発酵槽1に返される。14は精
留塔8の塔底液の取り出しラインである。
次にこの発明の方法を第2図に従つて説明す
る。同図において第1図の場合と同様にフイード
ライン2を通じて発酵槽1に供給された発酵原料
は発酵反応により発酵生産物を生産し、ガス状の
生産物(例えばCO2)はベントライン3を通じて
排出される。揮発性の発酵生産物を含む発酵液
は、発酵液抜き出しライン15を通じて、熱交換
器内蔵蒸発器16に導かれ、揮発性の発酵生産物
に富む蒸気と発酵熱を放出して、熱交換器内蔵蒸
発器16の減圧度に対応する発酵液の沸点にまで
冷却された後、発酵液戻りライン17を通じて発
酵槽1に還流される。
熱交換器内蔵蒸発器16は、流下薄膜式熱交換
器のように伝熱面で液静水頭の発生しない構造と
なつているから、この蒸発器内で、発酵液の温度
は、所定減圧度下に沸点に維持されており、これ
は発酵温度より低いので発酵反応に関与する菌体
の活性を低下させることがない。
次に熱交換器内蔵蒸発器16で放出した揮発性
の発酵生産物に富む蒸気は、蒸発蒸気ライン18
を通り、蒸気圧縮機19で圧縮昇温後、圧縮蒸気
ライン20を通じて熱交換器内蔵蒸発器16に加
熱媒体として供給され、伝熱面を介して発酵液に
熱を供給するとともに、自らは凝縮し、凝縮蒸気
ライン21を経て系外に取り出される。
以上のようにこの発明は、発酵槽より発酵液の
一部を抜き出し、減圧下で運転される熱交換器内
蔵蒸発器に導き、揮発性発酵生産物に富む蒸気を
発生させて発酵生成物を気相中に移行させ、この
発酵生成物の蒸気を断熱圧縮して蒸発器の熱源と
して利用することを特徴とするもので、下記のよ
うに優れた作用効果を奏する。
(1) 揮発性発酵生産物を、発酵熱と蒸発蒸気の圧
縮による凝縮熱とを利用して、発酵液から分離
濃縮し、凝縮回収でき、実質的には、蒸発蒸気
の圧縮に要するわずかのエネルギーで発酵生産
物の濃縮回収を行うことができ、従来の蒸留法
より遥かに少ないエネルギーで蒸留を行うこと
ができる。
したがつて、この発明は、現在世界的に注目
されてきているバイオマスからのエネルギー生
産におけるプロセスに投入するエネルギーが生
産されるエネルギーより大きく、真のエネルギ
ー生産にならないという問題点を克服する意味
で寄与するところが大きい。
(2) 特に前記ATPALプロセスと比べても、発酵
液を、さらに昇温することを要しないため、熱
的シヨツクにより、発酵反応に関与する菌体の
損傷や活性低下をもたらすことがない。また蒸
発器に熱交換器を内蔵しているため、循環液量
も少なくてよく、伝熱効率が高いため伝熱面積
が小さくてすむ。
(3) さらにATPALプロセスでは、精留塔出口蒸
気をフラツシユ蒸発器の前段の熱交換器の熱源
として導入しており、実際の操作上、双方の運
転を常に調和させなければならず困難性が避け
られないのに対し、この発明では、単一機器内
で蒸気圧縮法を用いるので、実際上の操作が容
易である。
(4) また、ストリツピングタワーのように圧損の
ある蒸留装置を使用せず、圧損(液静水頭分)
のない構造の蒸発器を用いるので、減圧に要す
る圧力が少ない。さらに蒸発器を出た蒸気は、
自からは蒸発器で冷却されて液化するので冷却
水が不要である。
(5) 発酵生産物を連続的に系外に取り出すことが
できるので、発酵プロセスの連続化が容易に行
える。
(6) さらにアルコール発酵のような生成物阻害
(生産されたアルコールが酵母の活性を低下さ
せる)がある場合でも、生成物を連続的に抜き
出しているため生成物阻害を防止することがで
き、発酵速度を高く保つことができる。
次に本発明を実施例に基づきさらに詳細に説明
する。
実施例
第2図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。
エタノール5.9重量%とパン酵母を含有し、35
℃に保たれた発酵液26000gを有する発酵槽1に
フイードライン2より、33重量%濃度のグルコー
ス水溶液を毎時1511gずつ加え、一方発酵液抜き
出しライン15から毎時24000gの発酵液を抜き
出し、44torrに減圧された熱交換器内蔵蒸発器1
6に導き、蒸発器16よりエタノール濃度20.2重
量%の含水エタノール蒸気を毎時1276g得た。
発酵液は減圧熱交換器内蔵蒸発器16内で32℃
まで冷却されて、発酵槽1に返送され、発酵槽1
は外部から別の手段で冷却することなしに35℃±
1℃に保たれ、発酵槽1中のエタノール濃度は
5.9±0.5重量%に維持された。
蒸発器16で得られた含水エタノール蒸気は蒸
気圧縮機19で断熱圧縮されて40℃まで昇温さ
れ、蒸発器16内の熱交換器の加熱源として利用
され、自身は冷却されて凝縮液と未凝縮蒸気の混
相流が得られた。混相流中の凝縮液の割合は85重
量%であつた。
このときの蒸発器16に組み込まれた熱交換器
の伝熱面積は0.02m2で、十分な熱交換性能が達せ
られた。
比較例
第1図に示したフローシートに従がいエタノー
ル発酵を行つた。
実施例1と同様の発酵液を有する発酵槽1に33
重量%のグルコース水溶液を毎時1511gずつ加
え、発酵液抜き出しライン4から毎時82000gの
発酵液を抜き出し、熱交換器5で37℃まで加熱後
44torrに減圧されたフラツシユ蒸発器6に送入
し、エタノール20.2重量%の含水エタノール蒸気
を毎時1276gで得た。
発酵液は減圧されたフラツシユ蒸発器6内で32
℃まで冷却され発酵槽1に返送され、発酵槽1は
外部から別の手段で冷却することなしに、35℃±
1℃に保たれ、また発酵槽1中のエタノール濃度
は5.9±0.5重量%に保たれた。
フラツシユ蒸発器6で得られた含水エタノール
蒸気は蒸気圧縮機10で40℃まで断熱圧縮により
昇温され、熱交換器5の加熱源として使用され
て、自身は冷却されて凝縮液と凝縮蒸気の混相流
が得られた。混相流中の凝縮液の割合は85重量%
であつた。
このとき、熱交換器5の熱交換性能を十分にす
るには、伝熱面積0.13m2が必要であつた。
実施例及び比較例の結果をまとめて次表に示
す。
The present invention relates to a method for producing fermentation products such as ethanol, acetone, butanol, etc. by effectively utilizing the thermal energy of fermentation liquid. Fermentation processes using microorganisms have the advantage of being able to carry out synthesis reactions at room temperature and pressure, compared to chemical synthesis methods that have been widely used in the past, but generally produce the desired product at a low concentration (10 %
1-2% in acetone butanol fermentation),
Therefore, it has the disadvantage that a large amount of energy is consumed to concentrate and separate it. On the other hand, at present, however, the heat generated by microorganisms during fermentation reactions, that is, reaction heat, is usually simply removed using shower coolers, flash coolers, cooling coils, and the like. In ethanol fermentation, this generated heat is expressed as follows:
Reaching 26Kcal/mol glucose. This amounts to about 1/4 of the amount of heat required to strip ethanol from, for example, a 10% aqueous ethanol solution. C 6 H 12 O 6 →2C 2 H 5 OH + CO 2 + 26 Kcal/mol glucose Various methods and devices have been proposed to improve the drawbacks of this fermentation process. For example, in the fermentation production of ethanol, a fermentation tank or a flash tank combined with a fermentation tank is depressurized to remove ethanol-rich evaporation (US Pat. No. 2,440,925). There is a method (Japanese Patent Publication No. 39-26041) that removes it by circulating it. However, in this method, the extracted steam is cooled in a condenser, which still results in heat loss. There are also other problems, such as the need for power to compress the condenser to normal pressure during cooling, and the need for deep cooling to cool the condenser. The other method is intended to concentrate the fermentation liquid, and has the disadvantage that only the volatile fermentation product (+water) can be obtained in an amount corresponding to the calorific value of the fermentation reaction. Furthermore, with respect to these conventional techniques, there is a severe debate as to whether the energy required to produce fermentation products such as ethanol is greater than the energy contained in fermentation products such as ethanol. Therefore, as a particularly low-cost ethanol fermentation method, a portion of the liquid extracted from the fermenter is heated through a heat exchanger, and then guided to a vacuum flash evaporator.
The ethanol-rich vapor is taken out into the gas phase, which is led to a vacuum rectification column to produce azeotropic ethanol (95vol%
ethanol), and then adiabatically compresses the vapor at the top of the rectification column using a compressor to use it as a heat source for the rectification column and a heat source for the heat exchanger at the front stage of the vacuum flash evaporator (ATPAL method, Chem.Age,
Nov. 21, (1980) p11) is proposed. However, in this method, the amount of heat required to evaporate the ethanol is transported in the form of sensible heat from the heat exchanger to the vacuum flash evaporator, so the amount of circulating fermentation liquid is large and the required heat transfer area of the heat exchanger is also large. It had the following drawbacks. Furthermore, a disadvantage of this method is that if fermentation is already carried out at the maximum temperature at which microorganisms (bacterial cells) can be active in order to increase the fermentation rate in the fermenter, the fermentation liquid may be further heated with a heat exchanger. The microbial cells in the fermentation broth are subjected to a thermal shock, which can stop their activity and cause irreversible damage. In order to overcome the shortcomings and problems of these conventional methods, the inventors conducted various studies, and as a result, they extracted a portion of the fermentation liquid containing fermentation products from the fermenter,
This is led to an evaporator with a built-in heat exchanger whose pressure is reduced to below the vapor pressure at the fermentation temperature, where volatile (boiling point lower than water) fermentation products are evaporated, and the steam containing this fermentation product is compressed and heated. If this is used as a heating source for an evaporator with a built-in heat exchanger, the above objectives can be achieved: removal of fermentation reaction heat, effective use of the reaction heat for evaporation, and energy-saving evaporation concentration of fermentation products without damaging bacterial cells. found that it can be achieved. This invention has been completed based on this knowledge. That is, the present invention extracts a part of the fermentation liquid containing volatile fermentation products from the fermenter and depressurizes it below the vapor pressure at the fermentation temperature, thereby performing heat exchange in which a liquid hydrostatic head is not substantially generated. circulates to the built-in evaporator to generate volatile fermentation product vapor,
The present invention provides a method for producing a volatile fermentation product, which is characterized in that the vapor is adiabatically compressed, heated, and used as a heating source for an evaporator with a built-in heat exchanger. In this invention, there is no particular restriction on the type of evaporator with a built-in heat exchanger used, but the heat exchanger may be a falling film type, a falling thin film type, a thin film type (horizontal tube type),
Types such as the Luwa type, which have a structure in which virtually no hydrostatic head is generated, are used because they have good cooling efficiency for the fermentation liquid. The evaporator with a built-in heat exchanger is operated at a reduced pressure below the vapor pressure at the fermentation temperature (a degree of vacuum at which the fermentation liquor containing volatile fermentation products boils below the fermentation temperature). The specific degree of pressure reduction varies depending on the type of fermentation reaction and the fermentation temperature of the fermenter at that time, but it is usually
It ranges from 720 to 20 torr, preferably from 150 to 30 torr. To put this more specifically, in ethanol fermentation, the maximum temperature at which fermentation can be practically carried out with current yeast (Saccharomyces genus) is around 35°C at normal pressure, but when the ethanol concentration is 6% by volume, the pressure is reduced to 50 torr. It is preferable to do so. The fermentation temperature, that is, the temperature of the fermentation liquid in the fermenter, varies depending on the type of fermentation reaction, but is usually between 20 and 80℃.
℃ range, preferably 30 to 65℃ range. In this invention, the rate of withdrawal of the fermented liquor from the fermenter is 10%/10% of the fermented liquor retained in the fermenter.
A range of 180% per hour to 180% per hour is preferred. The fermented liquor from which volatile fermentation products have been removed by evaporation in the evaporator with a built-in heat exchanger is circulated to the fermenter after fermentation heat is also removed by evaporation. Therefore, the fermentation reaction can proceed smoothly by cooling the fermenter, and fermentation inhibition can be reduced by removing fermentation products. On the other hand, the vapor rich in volatile fermentation products removed by evaporation in the evaporator with a built-in heat exchanger is compressed adiabatically, and after increasing the temperature and pressure, it is heated by the evaporator with a built-in heat exchanger. used as a liquid, it is cooled and liquefied in its evaporator. After adiabatic compression, the temperature of the vapor rich in volatile fermentation products is 3 to 20°C higher than the temperature of the fermentation liquor in the fermenter. The method of this invention can be applied to ethanol fermentation, acetone butanol fermentation, etc. Next, the present invention will be explained in more detail with reference to the drawings. Figure 1 shows the conventional ATPAL method described above.
A process flow sheet is shown, and FIG. 2 shows a flow sheet as one embodiment of the method of the present invention. In Figure 1, feed line 2 is connected to fermenter 1.
The fermentation raw material is supplied through
CO 2 ) is exhausted through vent line 3. The fermentation liquor containing volatile products is extracted through the fermentation liquor withdrawal line 4, heated in a heat exchanger 5, and then sent to a flash evaporator 6 where it is subjected to flash evaporation treatment. Vapor rich in volatile products separated by this flash evaporation is sent to a rectification column 8 via a line 7, and vapor of volatile products is sent to a vapor compressor 10 via a rectification column overhead vapor line 9.
This compressed steam is sent to the heat exchanger 5 through the line 11 and used as a heating source for the heat exchanger 5.
2, it is taken out as condensed steam. On the other hand, the fermentation liquor which has released vapor rich in volatile products is returned to the fermenter 1 through the fermentation liquor return line 13. 14 is a line for taking out the bottom liquid of the rectification column 8. Next, the method of the present invention will be explained with reference to FIG. In the same figure, as in the case of FIG. 1, the fermentation raw material supplied to the fermenter 1 through the feed line 2 undergoes a fermentation reaction to produce fermentation products, and gaseous products (e.g. CO 2 ) are discharged through the vent line 3. be done. The fermentation liquor containing volatile fermentation products is led to the evaporator 16 with a built-in heat exchanger through the fermentation liquor withdrawal line 15, where it releases steam rich in volatile fermentation products and fermentation heat, and passes through the heat exchanger. After being cooled to the boiling point of the fermentation liquor corresponding to the degree of pressure reduction in the built-in evaporator 16, the fermentation liquor is returned to the fermentation tank 1 through the fermentation liquor return line 17. The evaporator 16 with a built-in heat exchanger has a structure that does not generate a liquid hydrostatic head on the heat transfer surface like a falling film heat exchanger, so the temperature of the fermented liquid within this evaporator is maintained at a predetermined degree of vacuum. The boiling point is maintained below the fermentation temperature, so it does not reduce the activity of the bacteria involved in the fermentation reaction. Next, the steam rich in volatile fermentation products discharged from the evaporator 16 with a built-in heat exchanger is transferred to the evaporative steam line 18.
After being compressed and heated by the vapor compressor 19, it is supplied as a heating medium to the evaporator 16 with a built-in heat exchanger through the compressed vapor line 20, supplying heat to the fermentation liquid via the heat transfer surface, and condensing itself. Then, it is taken out of the system via the condensed steam line 21. As described above, the present invention extracts a portion of the fermentation liquid from the fermenter, guides it to the evaporator with a built-in heat exchanger operated under reduced pressure, generates steam rich in volatile fermentation products, and removes the fermentation products. This method is characterized by transferring the fermentation product into the gas phase, adiabatically compressing the vapor of the fermentation product, and using it as a heat source for the evaporator, and has excellent effects as described below. (1) Volatile fermentation products can be separated and concentrated from the fermentation liquid and condensed and recovered using the heat of fermentation and the heat of condensation resulting from the compression of evaporated steam. Fermentation products can be concentrated and recovered using energy, and distillation can be performed using far less energy than traditional distillation methods. Therefore, this invention is intended to overcome the problem of energy input from biomass, which is currently attracting worldwide attention, where the energy input into the process is greater than the energy produced, resulting in no true energy production. There is a lot to contribute. (2) Especially compared to the above-mentioned ATPAL process, there is no need to further raise the temperature of the fermentation liquid, so thermal shock does not damage or reduce the activity of microbial cells involved in the fermentation reaction. Furthermore, since the evaporator has a built-in heat exchanger, the amount of circulating fluid can be small, and the heat transfer efficiency is high, so the heat transfer area can be small. (3) Furthermore, in the ATPAL process, the steam at the outlet of the rectification column is introduced as a heat source for the heat exchanger before the flash evaporator, and in actual operation, the operation of both must always be harmonized, which is difficult. In contrast, the present invention uses vapor compression within a single piece of equipment, making it easier to operate in practice. (4) In addition, without using a distillation device that has a pressure drop like a stripping tower, the pressure drop (liquid hydrostatic head)
Since an evaporator with no structure is used, less pressure is required for depressurization. Furthermore, the steam leaving the evaporator is
Since it is cooled by itself in an evaporator and liquefied, no cooling water is required. (5) Fermentation products can be continuously taken out of the system, making it easy to make the fermentation process continuous. (6) Furthermore, even if there is product inhibition such as in alcoholic fermentation (produced alcohol reduces yeast activity), product inhibition can be prevented because the product is continuously extracted. Fermentation speed can be kept high. Next, the present invention will be explained in more detail based on examples. EXAMPLE Ethanol fermentation was carried out according to the flow sheet of the present invention shown in FIG. Contains 5.9% ethanol and baker's yeast, 35% by weight
To the fermenter 1 containing 26,000 g of fermentation liquid kept at ℃, 1,511 g of a 33% by weight glucose aqueous solution was added per hour through the feed line 2, while 24,000 g of fermentation liquid per hour was drawn out from the fermentation liquid extraction line 15, and the pressure was reduced to 44 torr. Evaporator with built-in heat exchanger 1
6, and 1276 g of water-containing ethanol vapor with an ethanol concentration of 20.2% by weight was obtained from the evaporator 16 per hour. The fermentation liquid is heated to 32℃ in the evaporator 16 with a built-in vacuum heat exchanger.
It is cooled down to
±35°C without external cooling by other means
The temperature is maintained at 1℃, and the ethanol concentration in fermenter 1 is
It was maintained at 5.9±0.5% by weight. The water-containing ethanol vapor obtained in the evaporator 16 is adiabatically compressed in the vapor compressor 19, heated to 40°C, and used as a heating source for the heat exchanger in the evaporator 16, and is cooled and converted into a condensate. A multiphase flow of uncondensed vapor was obtained. The proportion of condensate in the multiphase flow was 85% by weight. The heat transfer area of the heat exchanger incorporated in the evaporator 16 at this time was 0.02 m 2 , and sufficient heat exchange performance was achieved. Comparative Example Ethanol fermentation was carried out according to the flow sheet shown in FIG. 33 to fermenter 1 having the same fermentation liquid as in Example 1.
% glucose aqueous solution was added per hour, 82000 g of fermented liquid was extracted per hour from the fermented liquid extraction line 4, and heated to 37°C in the heat exchanger 5.
The mixture was fed into a flash evaporator 6 whose pressure was reduced to 44 torr to obtain 1276 g/hour of water-containing ethanol vapor containing 20.2% by weight of ethanol. The fermented liquid is stored in a depressurized flash evaporator 6.
℃ and returned to fermenter 1, which is then cooled to 35℃± without external cooling by other means.
The temperature was maintained at 1° C., and the ethanol concentration in fermenter 1 was maintained at 5.9±0.5% by weight. The water-containing ethanol vapor obtained in the flash evaporator 6 is heated to 40°C by adiabatic compression in the vapor compressor 10, and is used as a heating source for the heat exchanger 5, where it is cooled and separated into condensed liquid and condensed vapor. A multiphase flow was obtained. The proportion of condensate in the multiphase flow is 85% by weight
It was hot. At this time, in order to obtain sufficient heat exchange performance of the heat exchanger 5, a heat transfer area of 0.13 m 2 was required. The results of Examples and Comparative Examples are summarized in the following table.
【表】
蒸気
[Table] Steam
第1図は従来の発酵生産物の製造方法の1例を
示すフローシート、第2図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、1……発酵槽、2……フイードラ
イン、3……ベントライン、15……発酵液抜き
出しライン、16……熱交換器内蔵蒸発器、17
……発酵液戻りライン、18……蒸発蒸気ライ
ン、19……蒸気圧縮器、20……圧縮蒸気ライ
ン、21……凝縮蒸気ライン。
FIG. 1 is a flow sheet showing an example of a conventional method for producing fermented products, and FIG. 2 is a flow sheet showing an example of the method for producing fermented products of the present invention. Explanation of symbols, 1... Fermentation tank, 2... Feed line, 3... Vent line, 15... Fermented liquor extraction line, 16... Evaporator with built-in heat exchanger, 17
... Fermentation liquid return line, 18 ... Evaporation steam line, 19 ... Vapor compressor, 20 ... Compressed steam line, 21 ... Condensed steam line.
Claims (1)
酵液の一部を抜出し、これを発酵温度での蒸気圧
以下に減圧した、液静水頭が実質的に発生しない
熱交換器内蔵蒸発器に循環して、揮発性発酵生産
物を蒸発させ、この蒸気を断熱圧縮して昇温させ
その熱交換器内蔵蒸発器の加熱源とすることを特
徴とする揮発性発酵生産物の製造法。 2 熱交換器内蔵蒸発器が流下膜式流下薄膜式、
水平管型の薄膜式又はLuwa型の構造のものであ
る特許請求の範囲第1項記載の揮発性発酵生産物
の製造法。 3 揮発性発酵生産物がエタノール、アセトン又
はブタノールである特許請求の範囲第1項記載の
揮発性発酵生産物の製造方法。[Scope of Claims] 1 A part of the fermentation liquid containing volatile fermentation products is extracted from the fermenter and the pressure is reduced to below the vapor pressure at the fermentation temperature, thereby generating heat that substantially does not generate a liquid hydrostatic head. Volatile fermentation production characterized by circulating to an evaporator with a built-in exchanger to evaporate the volatile fermentation product, adiabatically compressing this vapor to raise the temperature, and using the vapor as a heating source for the evaporator with a built-in heat exchanger. How things are manufactured. 2 The evaporator with built-in heat exchanger is a falling film type falling film type,
The method for producing a volatile fermentation product according to claim 1, which has a horizontal tube type thin film type or Luwa type structure. 3. The method for producing a volatile fermentation product according to claim 1, wherein the volatile fermentation product is ethanol, acetone, or butanol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56150673A JPS5856688A (en) | 1981-09-25 | 1981-09-25 | Production of volatile fermentation product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56150673A JPS5856688A (en) | 1981-09-25 | 1981-09-25 | Production of volatile fermentation product |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5856688A JPS5856688A (en) | 1983-04-04 |
| JPS6338191B2 true JPS6338191B2 (en) | 1988-07-28 |
Family
ID=15501966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56150673A Granted JPS5856688A (en) | 1981-09-25 | 1981-09-25 | Production of volatile fermentation product |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5856688A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI118301B (en) * | 2005-05-25 | 2007-09-28 | St1 Biofuels Oy | Process for preparing an ethanol-water mixture |
| RU2405830C2 (en) * | 2009-02-18 | 2010-12-10 | Дэвон Инвестмент Лимитед | Method of preparing organic solvents |
| JP7033593B2 (en) * | 2016-11-29 | 2022-03-10 | ピュラック バイオケム ビー. ブイ. | Fermentation process |
| DE102017207634A1 (en) * | 2017-05-05 | 2018-11-08 | Siemens Aktiengesellschaft | Apparatus and process for fermentation |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5621592A (en) * | 1979-07-18 | 1981-02-28 | Rolls Royce | Method and apparatus for producing organic compound by fermentation |
-
1981
- 1981-09-25 JP JP56150673A patent/JPS5856688A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5856688A (en) | 1983-04-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103566613B (en) | A kind of low-concentration organic solvent aqueous solution reclaims heat pump distillation apparatus and technique | |
| US4617270A (en) | Alcohol and distillers grain recovery process | |
| US4822737A (en) | Process for producing ethanol by fermentation | |
| US4399000A (en) | Process for producing absolute alcohol by solvent extraction and vacuum distillation | |
| CN102936198B (en) | Produce the method for vinyl acetate | |
| GB2054643A (en) | Fermentation process for the manufacture of an organic compound | |
| CN110407173A (en) | A kind of waste acid treatment system and the method using system processing spent acid | |
| JPS6338191B2 (en) | ||
| EP0050662A1 (en) | Process and apparatus for continuous production of ethanol | |
| CN100551895C (en) | A method for recovering acetic acid from acetic acid-containing wastewater | |
| JPS56100736A (en) | Purifying method of monochloroacetic acid | |
| JPH0547485B2 (en) | ||
| CN209836040U (en) | Potassium tert-butoxide indirect compression self-backheating rectification system | |
| JPS6239541A (en) | Formic acid production equipment | |
| CN203474692U (en) | Efficient and energy-saving preparation device of acetyl acetone | |
| JPH0369274B2 (en) | ||
| CN103333063B (en) | High-efficiency energy-saving preparation method and preparation device of acetylacetone | |
| RU2230788C2 (en) | Method for continuous preparing ethyl alcohol | |
| JPS5888002A (en) | distillation equipment | |
| CN223311677U (en) | Full-baffle thermal coupling rectifying system | |
| CN224133049U (en) | Product extraction device for producing acetone by pressure fermentation of synthesis gas | |
| CN222173101U (en) | Distillation coupled concentration and decolorization device | |
| JPS6336753B2 (en) | ||
| JPS58183634A (en) | Production of anhydrous ethanol through multiple effect process | |
| JPH031000B2 (en) |