JP2007111590A - Method for manufacturing ethanol from kitchen garbage - Google Patents
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- JP2007111590A JP2007111590A JP2005303337A JP2005303337A JP2007111590A JP 2007111590 A JP2007111590 A JP 2007111590A JP 2005303337 A JP2005303337 A JP 2005303337A JP 2005303337 A JP2005303337 A JP 2005303337A JP 2007111590 A JP2007111590 A JP 2007111590A
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 88
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title abstract description 12
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- 229920002472 Starch Polymers 0.000 claims abstract description 10
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- 239000002054 inoculum Substances 0.000 claims description 6
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- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
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Abstract
Description
地球温暖化が進行する一方、石油資源の枯渇も同時並行で進んでおり、石油の消費を抑制し、エネルギー源を光合成産物である再生可能資源に置き換えていくことが人類共通の課題となっている。二酸化炭素削減にかかわる京都議定書の目標達成に向け、我が国でもガソリンに再生可能資源から生産したバイオエタノールを添加することが決定された。 While global warming is progressing, oil resources are depleting at the same time, and it is a common challenge for mankind to control oil consumption and replace energy sources with renewable resources, which are photosynthetic products. Yes. In order to achieve the target of the Kyoto Protocol related to carbon dioxide reduction, it was also decided in Japan to add bioethanol produced from renewable resources to gasoline.
しかしながら、我が国には、エタノール生産可能であり、かつ需要に見合うだけの安価な農産物が存在しない。そこで、建築廃材や風倒木など木材資源を糖化してエタノールを生産する技術開発が盛んに行われているが、技術的に高いハードルがあり、未だ経済性の目処が立っていない。 However, in Japan, there are no cheap agricultural products that can produce ethanol and meet demand. Therefore, technology development to produce ethanol by saccharifying wood resources such as building waste materials and wind-fall trees has been actively carried out, but there are technically high hurdles and there is still no economic prospect.
エタノールは、清酒、焼酎、ビール、ワイン、ウイスキーなど全ての酒類の主成分であり、古来、酵母による発酵法によって生産されている。また、工業用、燃料用のものも、農産物資源の豊富なアメリカやブラジルにおいて、発酵法によって生産されている。因みに、ブラジルでは25%、アメリカでは10%のバイオエタノール(発酵エタノール)がガソリンに添加されている。 Ethanol is the main component of all alcoholic beverages such as sake, shochu, beer, wine and whiskey, and has been produced by fermentation using yeast since ancient times. Industrial and fuel products are also produced by fermentation in the United States and Brazil, where agricultural resources are abundant. Incidentally, 25% of bioethanol (fermented ethanol) is added to gasoline in Brazil and 10% in the United States.
発酵法によると、原料の組成と品質は、制約を受ける。酵母の増殖とアルコールを生産させる微生物の代謝反応を正確に行わせるためである。即ち、原料を峻別しなければ、効率の良いアルコール発酵は行えない。 According to the fermentation method, the composition and quality of the raw materials are limited. This is in order to accurately perform the growth of yeast and the metabolic reaction of microorganisms that produce alcohol. In other words, efficient alcoholic fermentation cannot be performed unless the raw materials are distinguished.
例えば、アメリカではとうもろこしデンプン(コーンスターチ)が、ブラジルではサトウキビから得られるケインモラセスや粗糖シロップが大量に得られるため、燃料用エタノール生産のための発酵事業が可能になっている。 For example, corn starch (cornstarch) can be obtained in large quantities in the United States, and cane molasses and crude syrup obtained from sugarcane in Brazil, making it possible to conduct fermentation for the production of fuel ethanol.
さて、エタノール生成細菌Zymomonas mobilisは、メキシコの地酒プルケの醸造に関与する微生物である。そのアルコール生産速度は、非常に大きいが、工業用エタノールの生産に用いられている例はない。なぜなら、エタノール生成細菌Zymomonas mobilisは、増殖にアミノ酸やビタミン類を必要とし、培地の栄養成分が複雑なためである。 Now, the ethanol-producing bacterium Zymomonas mobilis is a microorganism involved in the brewing of the Mexican local sake Purke. Although its alcohol production rate is very high, there is no example used for production of industrial ethanol. This is because the ethanol-producing bacterium Zymomonas mobilis requires amino acids and vitamins for growth and the nutrient components of the medium are complex.
生ゴミは、我が国国内だけで年間2,000万トン(農林水産省統計)も発生している貴重な資源であり、これを有効活用しようとする技術開発は各視点から検討されている。しかしながら、エネルギー回収を目的とするものは、生ゴミを脱水し自燃や嫌気性メタン発酵処理によるものが中心である。 Garbage is a valuable resource that generates 20 million tons per year (Ministry of Agriculture, Forestry and Fisheries statistics) in Japan alone, and technological development to make effective use of this is being considered from various viewpoints. However, what is aimed at energy recovery is mainly by dehydration of raw garbage and self-combustion or anaerobic methane fermentation.
液体燃料化によるエネルギー回収法については、本発明者らによる生ゴミを原料にしたアセトン・ブタノール発酵の開発例があるにすぎない。アセトン・ブタノール発酵では、炭水化物(グルコース)からブタノールを生成する収率(転換率)は、重量ベースで22%程度である。生ゴミを原料とするエネルギー回収法において、さらなる効率をあげうる技術開発が求められている。
そこで本発明は、生ゴミを原料とし、しかも高い効率でエタノールを回収できる方法を提供することを目的とする。 Accordingly, an object of the present invention is to provide a method that can recover ethanol with high efficiency using raw garbage as a raw material.
第1の発明に係るエタノール生産法は、生ゴミを粉砕して粉砕物を生成するステップと、粉砕物のデンプン濃度を調整し糖化酵素を加え糖化処理水を生成するステップと、糖化処理水に予め培養したZymomonas mobilisの種菌を接種してアルコール発酵させ、もろみを生成するステップと、もろみを蒸留してエタノールを回収するステップとを含む。 The ethanol production method according to the first invention includes a step of pulverizing raw garbage to generate a pulverized product, a step of adjusting the starch concentration of the pulverized product and adding a saccharifying enzyme to generate saccharified treated water, and Inoculating a pre-cultured Zymomonas mobilis inoculum and subjecting it to alcohol fermentation to produce mash, and a step of distilling the mash to recover ethanol.
第2の発明に係るエタノール生産法では、第1の発明に加え、粉砕物を生成するステップにおいて、生ゴミに水が加えられる。 In the ethanol production method according to the second invention, in addition to the first invention, water is added to the raw garbage in the step of generating a pulverized product.
第3の発明に係るエタノール生産法では、第1の発明に加え、糖化処理水を生成するステップにおいて、デンプン濃度調整後糖化酵素を加え、糖化反応を行って後濾過するか、あるいはそのまま用いる。 In the ethanol production method according to the third invention, in addition to the first invention, in the step of producing saccharified water, a saccharification enzyme is added after adjusting the starch concentration, and a saccharification reaction is carried out, followed by filtration or used as it is.
第4の発明に係るエタノール生産法では、第1の発明に加え、糖化処理水を生成するステップにおいて、デンプン濃度調整後糖化酵素を加え、糖化処理して得た糖化液又はそれを濾過して得た液を滅菌処理して用いる。 In the ethanol production method according to the fourth invention, in addition to the first invention, in the step of producing saccharified water, a saccharification enzyme obtained after saccharification treatment by adding a saccharification enzyme after adjusting the starch concentration or filtering it is filtered. The liquid obtained is sterilized before use.
第5の発明に係るエタノール生産法では、第1の発明に加え、対ブドウ糖転換率は、48%である。 In the ethanol production method according to the fifth invention, in addition to the first invention, the glucose conversion rate is 48%.
本発明によれば、生ゴミを原料とし、しかも高い効率でエタノールを回収できる。光合成産物である生ゴミの大部分は、有効利用されることなく焼却されまたは投棄されているが、本発明によれば、生ゴミから効率よくエタノールを生産でき、我が国におけるガソリン添加用エタノール生産に資することができる。 According to the present invention, it is possible to recover ethanol with high efficiency using raw garbage as a raw material. Most of the garbage that is a photosynthetic product is incinerated or dumped without being effectively used, but according to the present invention, ethanol can be efficiently produced from the garbage, and it can be used in the production of ethanol for gasoline addition in Japan. Can contribute.
本発明の概要は、次のとおりである。 The outline of the present invention is as follows.
生ゴミに対して、特別の分別作業を行わず、生ゴミから、金属片、プラスチックなどを取り除き、これを粉砕する。具体的には、生ゴミから金属、プラスチック、ラップシート、アルミホイール、割り箸など微生物によって資化できない物質や糖化酵素によって分解されない物質を取り除く。但し、食品として供せられたものの残飯、および食卓に飾りとして供せられた野菜、果物、新鮮魚などは、粉砕機の刃を損傷しないかぎりとくに選別する必要はない。これらを少量の水を加えながら粉砕する。 Without any special separation work on the garbage, metal pieces, plastics, etc. are removed from the garbage and crushed. Specifically, metals, plastics, wrap sheets, aluminum wheels, disposable chopsticks and other substances that cannot be assimilated by microorganisms or substances that cannot be decomposed by saccharifying enzymes are removed from raw garbage. However, it is not necessary to select the leftovers of food provided as food, and vegetables, fruits, fresh fish, etc. provided as decorations on the table as long as the blades of the grinder are not damaged. These are pulverized while adding a small amount of water.
次に、粉砕物に、デンプン濃度調整後糖化酵素を加えて糖化処理し糖化処理水を生成する。 Next, a saccharification enzyme is added to the pulverized product after the starch concentration is adjusted, and saccharification treatment is performed to produce saccharification treated water.
具体的には、まず、粉砕物に水を加え、攪拌可能な粘度に調整する。ここで、調理された食品に含まれるデンプンは、すでにアルファ化されており、液化酵素による液化処理は不要だが、液の粘度が高くなることは避けられない。生ゴミの水分は約75%程度であるから、生ゴミと同量の水を加えて液状化しても、できあがった生ゴミ粉砕液に含まれるデンプンなど食品要素の乾物換算濃度は約12.5%程度にすぎず、これを糖化しても8−9%の糖濃度の糖液を得るのが精一杯である。 Specifically, first, water is added to the pulverized product to adjust the viscosity so that it can be stirred. Here, the starch contained in the cooked food is already pregelatinized, and liquefaction treatment with a liquefaction enzyme is not necessary, but it is inevitable that the viscosity of the liquid becomes high. Since the moisture of raw garbage is about 75%, even if it is liquefied by adding the same amount of water as raw garbage, the dry matter equivalent concentration of food elements such as starch contained in the finished garbage pulverized liquid is about 12.5. Even if it is saccharified, it is best to obtain a sugar solution having a sugar concentration of 8-9%.
さらに、調整された生ゴミ粉砕液を、使用する糖化酵素に至適なpHに調整し、糖化酵素を加えて至適温度で必要時間保ち糖化処理し、糖化処理水を生成する。 Furthermore, the adjusted garbage pulverized liquid is adjusted to a pH optimum for the saccharifying enzyme to be used, saccharifying enzyme is added, and the saccharification treatment is performed for a necessary time at an optimum temperature to generate saccharification treated water.
残飯を中心にした生ゴミは生野菜や果物を豊富に含み、これらに含まれるプロテアーゼの作用により、タンパク質の低分子化も促進される。このような比較的低濃度のブドウ糖液でしかもタンパク質も比較的大量に含む栄養豊富な基質は、酒造を目的としないかぎり、酵母による発酵よりもZymomonasによるアルコール発酵の方に適する。特にZymomonasによる連続発酵法は、アルコール濃度が比較的低い(例えば5−6%)場合、非常に大きい生産速度が得られるので、燃料用エタノールを生産する上で、大変有利となる。 Garbage, mainly leftovers, contains abundant raw vegetables and fruits, and the action of proteases contained in these also promotes low molecular weight proteins. Such a nutrient-rich substrate with a relatively low concentration of glucose solution and a relatively large amount of protein is more suitable for alcoholic fermentation by Zymomonas than for yeast. In particular, the continuous fermentation method by Zymomonas is very advantageous in producing ethanol for fuel because a very high production rate can be obtained when the alcohol concentration is relatively low (for example, 5-6%).
次に、この糖化処理水を、そのまま/もしくは濾過して、特別の栄養物を加えることなく滅菌処理のみを行う。Zymomonas mobilisの種菌を接種してエタノール発酵させ、もろみを生成する。さらに、もろみを蒸留してエタノールを回収する。その結果、対ブドウ糖48%の転換率でエタノールを生成できる。 Next, the saccharified water is subjected to sterilization only without adding special nutrients as it is / or filtered. Zymomonas mobilis is inoculated with ethanol and fermented to produce moromi. Further, the mash is distilled to recover ethanol. As a result, ethanol can be produced at a conversion rate of 48% with respect to glucose.
ここで、エタノール生成細菌Zymomonas mobilisは、細胞増殖とエタノール生成の為に基質となる糖のほか、各種の有機栄養素を必要とする。そのため、培養試験を行う標準培地では、糖に酵母エキスと麦芽エキスを配合したYM Broth(Difco)を使用する。これら栄養素は、主としてアミノ酸類、ビタミン類と考えられているが特定されてはいない。 Here, the ethanol-producing bacterium Zymomonas mobilis requires various organic nutrients in addition to sugar as a substrate for cell growth and ethanol production. For this reason, YM Broth (Difco) in which a yeast extract and a malt extract are mixed with sugar is used as a standard medium for performing a culture test. These nutrients are thought to be mainly amino acids and vitamins, but are not specified.
本発明者らは、生ゴミの中に含まれる魚や肉の成分がこの菌の増殖に有効に使用できるのではないかと期待して、鋭意研究を重ねた。また、生ゴミに混在するパイナップルなどの果実にはプロテアーゼ活性も存在することから、生ゴミはエタノールの原料となる糖質を供給するのみならず、動物タンパク質を分解する酵素源を含み、その働きによって、Zymomonas mobilisの増殖とアルコール生成に必要な有機栄養素をも供給することが可能な資源であるとの仮説に立って実験を行い効果を確認すると共に、本発明を完成したものである。 The inventors of the present invention have conducted extensive research in anticipation that the components of fish and meat contained in raw garbage can be used effectively for the growth of this bacterium. In addition, since fruits such as pineapples that are mixed in raw garbage also have protease activity, raw garbage not only supplies carbohydrates as a raw material for ethanol, but also contains an enzyme source that degrades animal proteins. Thus, the present invention was completed while confirming the effect by conducting experiments under the hypothesis that it is a resource capable of supplying organic nutrients necessary for the growth and alcohol production of Zymomonas mobilis.
以下、各実施例を挙げながら、本発明を更に具体的に説明するが、本発明は、これらの実施例に限定されるわけではない。 Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to these examples.
(実施例1)
種菌は、YMブロス(Difco Laboratories, Detroit)を培地とし、規定濃度に調整後試験管に10mlを分注し115℃で10分間加熱滅菌したもので調製した。これにZymomonas mobilis NRRL B−14023を接種し、30℃にて18時間静置培養したものを用いた。
Example 1
The inoculum was prepared using YM broth (Difco Laboratories, Detroit) as a medium, adjusted to a specified concentration, dispensed 10 ml into a test tube, and heat-sterilized at 115 ° C. for 10 minutes. This was inoculated with Zymomonas mobilis NRRL B-14023 and statically cultured at 30 ° C. for 18 hours.
生ゴミは、弁当残飯ごはん(しそ風味ふりかけに梅干し1ケ付き)120g、チキンカツ、ひじき煮物、こぼうと豚肉の煮物少々のおかず類120g、皮付きイチジク1切れ、巨峰ブドウ3個からなる果物100gを材料とした。 Raw garbage is 120 g of bento rice leftover rice (with a piece of shiso-flavored rice with a pickled plum), chicken cutlet, hijiki simmered, simmered pork and pork, 120 g of side dishes, 1 slice of figs with skin, 100 g of fruit consisting of 3 kyoho grapes Was used as a material.
これに水200mlを加えジューサーミキサーで皮や種子などがついたまま粉砕した。粉砕後さらに水を加えて全体を500mlとした。0.1N−NaOHでpHを4.5に調整した後糖化酵素Dextrozyme(Novo)100μlを加えもう一度ジューサーミキサーで全体を混合した。60℃で24h温水槽にて糖化反応を行った。糖化処理液の糖濃度(ブドウ糖換算)は92g/lであった。これをガーゼ布で巾着絞りで濾過したもの/および濾過せずそのままの液のもの各50mlずつ大型試験管に分注し、115℃10minオートクレーブ滅菌後上述の方法で調整した種菌を2.5ml接種して30℃15h培養した。発酵終了液のエタノールを分析したところ40.5g/lであった。 200 ml of water was added to this and pulverized with a juicer mixer with the skin and seeds attached. After pulverization, water was further added to make a total of 500 ml. After adjusting the pH to 4.5 with 0.1 N NaOH, 100 μl of saccharification enzyme Detrozyme (Novo) was added and the whole was mixed once again with a juicer mixer. The saccharification reaction was performed in a hot water bath at 60 ° C. for 24 hours. The sugar concentration (in terms of glucose) of the saccharification treatment solution was 92 g / l. 50 ml each of this filtered with a gauze cloth with a drawstring squeeze and / or unfiltered liquid is dispensed into a large test tube, sterilized at 115 ° C. for 10 min in an autoclave, and inoculated with 2.5 ml of the inoculum prepared by the above method And cultured at 30 ° C. for 15 hours. It was 40.5 g / l when ethanol of the fermentation end liquid was analyzed.
このようにして培養した培養液(もろみ)合計200mlを蒸留し、無水エタノール8mlを得た。 A total of 200 ml of the culture solution (moromi) thus cultured was distilled to obtain 8 ml of absolute ethanol.
(実施例2)
シード(種)に用いた菌、培地、発酵法、発酵条件は、実施例1と同一である。
(Example 2)
The bacteria, medium, fermentation method, and fermentation conditions used for the seeds are the same as in Example 1.
生ゴミは、サンドイッチ(玉子および野菜)110g、チーズピザ100g、パパイヤ(皮付き)100gを材料とした。 The raw garbage was made from 110 g of sandwich (egg and vegetables), 100 g of cheese pizza, and 100 g of papaya (with skin).
これに水200mlを加えジューサーミキサーでパパイヤの皮ごとそのまま粉砕した。粉砕後さらに水を加えて全体を500mlとした。0.1N−NaOHでpHを4.5に調整した後糖化酵素Dextrozyme(Novo)100μlを加えもう一度ジューサーミキサーで全体を混合した。60℃で24h温水槽にて糖化反応を行った。糖化処理液の糖濃度(ブドウ糖換算)は83g/lであった。これをガーゼ布で巾着絞りで濾過したもの/及び濾過せずそのままのもの各50mlずつ大型試験管に分注し、115℃10minオートクレーブ滅菌後上述の方法で調整した種菌を接種して30℃15h培養した。発酵終了液のエタノールを分析したところ36g/lであった。 200 ml of water was added thereto, and the papaya skin was pulverized as it was with a juicer mixer. After pulverization, water was further added to make a total of 500 ml. After adjusting the pH to 4.5 with 0.1 N NaOH, 100 μl of saccharification enzyme Detrozyme (Novo) was added and the whole was mixed once again with a juicer mixer. The saccharification reaction was performed in a hot water bath at 60 ° C. for 24 hours. The sugar concentration (in terms of glucose) of the saccharification treatment solution was 83 g / l. This was filtered with a gauze cloth with a drawstring squeezed and / or unfiltered, 50 ml each was dispensed into large test tubes, sterilized at 115 ° C. for 10 min and then inoculated with the inoculum prepared by the above method, and 30 ° C. for 15 h. Cultured. It was 36 g / l when ethanol of the fermentation finished liquid was analyzed.
このようにして培養した培養液(もろみ)合計200mlを蒸留し、無水エタノール7mlを得た。 A total of 200 ml of the culture solution (moromi) thus cultured was distilled to obtain 7 ml of absolute ethanol.
(実施例3)
種菌は、YMブロス(Difco Laboratories, Detroit)を培地とし、規定濃度に調整後試験管に10mlを分注し115℃で10分間加熱滅菌したもので調製したものにZymomonas mobilis NRRL B−14023を接種し、30℃にて18時間静置発酵したものをスターターとした。
(Example 3)
The inoculum was prepared by using YM broth (Difco Laboratories, Detroit) as a medium, dispensing 10 ml into a test tube after adjusting to a specified concentration, and heat-sterilizing at 115 ° C. for 10 minutes, then inoculating Zymomonas mobilis NRRL B-14003 Then, a starter was prepared by static fermentation at 30 ° C. for 18 hours.
これをブドウ糖50g/l、酵母エキス5g/l、KH2PO4 1g/lからなる培地を肉厚ガラス瓶に100ml入れて115℃で10分間加熱滅菌したシード培地に5mlシードし30℃にて15時間静置発酵した。 100 ml of a medium consisting of 50 g / l of glucose, 5 g / l of yeast extract, and 1 g / l of KH 2 PO 4 is placed in a thick glass bottle and seeded in 5 ml of a seed medium sterilized by heating at 115 ° C. for 10 minutes. Fermented for hours.
生ゴミは、懇親会立食パーティー残飯1kgすし類(巻きずし、たまご、えび、まぐろにぎりすし)、サンドイッチ(玉子、野菜、ハム)、鉢盛り皿(天ぷら、とりの唐揚げ)、果物(パイナップル、オレンジ)合計1kgを用いた。 Raw garbage is 1kg sushi from leftovers for social gatherings (sushi rolls, eggs, shrimp, tuna nigiri sushi), sandwiches (egg, vegetables, ham), bowls (tempura, fried chicken), fruits (pineapple, orange) ) A total of 1 kg was used.
これを飾りのビニールなどを取り除き水約1lを加えてそのまま粉砕した。粉砕後さらに水を加えて全体を2lとした。0.1N−NaOHでpHを4.5に調整した後糖化酵素Dextrozyme(Novo)500μlを加えスターラーで全体をよく混合攪拌した。60℃で24h温水槽にて糖化反応を行った。糖化処理液の糖濃度(ブドウ糖換算)は92g/lであった。これを3,000g 2min遠心分離し、清澄糖液1.8lを得た。この糖液をpH6.2に調整し115℃10minオートクレーブ滅菌後全容2.5lのガラスジャーファーメンターに入れ、上述のように調整したシード(100ml)を接種して30℃15h培養した。発酵中攪拌速度を150rpm pHを1N−NH4OHで5.5に制御した。培養16時間で発酵終了し、エタノール濃度を分析したところ42g/lであった。 The decorative vinyl or the like was removed, and about 1 liter of water was added and pulverized as it was. After pulverization, water was further added to make 2 l. After adjusting the pH to 4.5 with 0.1 N NaOH, 500 μl of saccharification enzyme Detrozyme (Novo) was added, and the whole was well mixed and stirred with a stirrer. The saccharification reaction was performed in a hot water bath at 60 ° C. for 24 hours. The sugar concentration (in terms of glucose) of the saccharification treatment solution was 92 g / l. This was centrifuged at 3,000 g for 2 min to obtain 1.8 l of a clarified sugar solution. The sugar solution was adjusted to pH 6.2, sterilized at 115 ° C. for 10 minutes, placed in a 2.5 liter glass jar fermenter, inoculated with the seed (100 ml) adjusted as described above, and cultured at 30 ° C. for 15 hours. During the fermentation, the stirring speed was 150 rpm. The pH was controlled to 5.5 with 1N-NH 4 OH. The fermentation was completed in 16 hours of culture, and the ethanol concentration was analyzed and found to be 42 g / l.
この培養液(もろみ)を蒸留し、無水エタノール80mlを得た。 This culture solution (moromi) was distilled to obtain 80 ml of absolute ethanol.
Claims (5)
前記粉砕物のデンプン濃度を調整し糖化酵素を加え糖化処理水を生成するステップと、
前記糖化処理水に予め培養したZymomonas mobilisの種菌を接種してアルコール発酵させ、もろみを生成するステップと、
前記もろみを蒸留してエタノールを回収するステップとを含む、生ゴミからのエタノール生産法。 Crushing raw garbage to produce a crushed material;
Adjusting the starch concentration of the pulverized product and adding a saccharifying enzyme to produce saccharified water;
Inoculating the inoculum of Zymomonas mobilis pre-cultured in the saccharified water and subjecting it to alcohol fermentation to produce moromi;
And a step of recovering ethanol by distilling the mash.
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WO2009141495A1 (en) * | 2008-05-20 | 2009-11-26 | St1 Biofuels Oy | Method and apparatus for processing waste containing fermentable raw material |
WO2010084589A1 (en) | 2009-01-22 | 2010-07-29 | 新日鉄エンジニアリング株式会社 | Method for recovering and producing ethanol and oil |
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