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CN102642993B - Alcohol fermentation wastewater treatment method - Google Patents

Alcohol fermentation wastewater treatment method Download PDF

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CN102642993B
CN102642993B CN 201210133467 CN201210133467A CN102642993B CN 102642993 B CN102642993 B CN 102642993B CN 201210133467 CN201210133467 CN 201210133467 CN 201210133467 A CN201210133467 A CN 201210133467A CN 102642993 B CN102642993 B CN 102642993B
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alcohols
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陈新德
黄超
熊莲
陈雪芳
张海荣
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Guangzhou Institute of Energy Conversion of CAS
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Abstract

本发明公开了一种醇类发酵废水的处理方法。它是先去除醇类发酵废水中固型物杂质,再调节醇类发酵废水的pH值为5.0~8.0,然后按接种量为2.5~20%(v/v)接入油脂酵母种子液,发酵温度为25~35℃,发酵时间为2~5天,进行好氧发酵,发酵结束后,收集废水中的酵母菌体,废水根据排放要求进行后续处理。按照本发明的方法处理醇类发酵废水,不仅处理效率高,COD去除率高,还能免除如传统厌氧、好氧活性污泥处理方法所需的长时间菌种驯化阶段,同时生产富含油脂、蛋白、核酸、番茄红素以及其它高附加值成分的酵母菌体,只需简单常规的好氧发酵设备,无需如厌氧活性污泥法等使用昂贵复杂的工艺设备,工艺简单,成本低廉。整个发酵过程无需添加任何营养物质,发酵周期较短。The invention discloses a treatment method for alcohol fermentation wastewater. It first removes the solid impurities in the alcohol fermentation wastewater, then adjusts the pH value of the alcohol fermentation wastewater to 5.0-8.0, and then inserts the oil yeast seed liquid according to the inoculation amount of 2.5-20% (v/v), and ferments The temperature is 25-35°C, the fermentation time is 2-5 days, and aerobic fermentation is carried out. After the fermentation is completed, the yeast cells in the wastewater are collected, and the wastewater is subjected to subsequent treatment according to the discharge requirements. According to the method of the present invention to treat alcohol fermentation wastewater, not only the treatment efficiency is high, the COD removal rate is high, but also the long-term bacteria domestication stage required by the traditional anaerobic and aerobic activated sludge treatment methods can be exempted, and the production of rich Yeast cells of oil, protein, nucleic acid, lycopene and other high value-added components only need simple and conventional aerobic fermentation equipment, and do not need expensive and complicated process equipment such as anaerobic activated sludge method. The process is simple and the cost is low. low. The whole fermentation process does not need to add any nutrients, and the fermentation period is short.

Description

一种醇类发酵废水的处理方法A kind of treatment method of alcohol fermentation waste water

技术领域: Technical field:

本发明涉及一种醇类发酵废水的处理方法,具体涉及一种利用油脂酵母发酵显著降低醇类发酵废水COD并同时生产高附加值酵母菌体的方法。The invention relates to a treatment method for alcohol fermentation wastewater, in particular to a method for significantly reducing the COD of alcohol fermentation wastewater and simultaneously producing high value-added yeast cells by using oily yeast fermentation.

背景技术: Background technique:

近年来,随着石油资源的枯竭,人类对新能源的探索日益增多。通过微生物发酵技术能生产大量的生物液体燃料如丁醇、乙醇等,是解决当前能源危机的一个有效出路。发酵结束后,通过简单的蒸馏技术,可以回收发酵液中的丁醇、乙醇以及丙酮等产物。然而剩下的发酵液富含丁酸、乙酸等有机酸,其COD往往在4000mg/L以上,因此需要后续的废水处理才能达到排放标准。In recent years, with the depletion of oil resources, human beings have increasingly explored new energy sources. A large amount of biological liquid fuels such as butanol and ethanol can be produced through microbial fermentation technology, which is an effective way to solve the current energy crisis. After fermentation, butanol, ethanol, acetone and other products in the fermentation broth can be recovered by simple distillation technology. However, the remaining fermentation broth is rich in organic acids such as butyric acid and acetic acid, and its COD is often above 4000mg/L, so subsequent wastewater treatment is required to meet the discharge standard.

油脂酵母(oleaginous yeast),即能利用各种碳源物质高产微生物油脂以及菌体蛋白的酵母,近年来开始被用于各种工业废水的处理。例如,北京化工大学的谭天伟课题组可用粘红酵母处理味精、淀粉、造纸等工业废水,并生产微生物油脂(Bioresour.Technol.2010,101:6092-5)。Venkata Subhash等利用油脂微生物处理玉米芯废水(Bioresour.Technol.,2011,102(19),9286-9290)。Yousuf等利用油脂酵母处理橄榄油废水等(J.Agric.Food Chem.,2010,58(15),8630-8635)。与上述发酵废水不同,醇类发酵废水富含丁酸、乙酸等有机酸,COD往往在4000mg/L以上。通常来说,使用内循环厌氧反应器(IC)并利用厌氧活性污泥能处理这种富含有机酸的发酵废水能达到一定的处理效果。但该工艺需要复杂的内循环厌氧反应器,建设成本较高。且活性污泥需要长达数个月的驯化才能达到处理效果,因而处理效率较低。Oleaginous yeast, a yeast that can use various carbon sources to produce high microbial oil and bacterial protein, has been used in the treatment of various industrial wastewater in recent years. For example, Tan Tianwei's research group at Beijing University of Chemical Technology can use Rhodotorula viscosus to treat industrial wastewater such as monosodium glutamate, starch, and papermaking, and produce microbial oils (Bioresour. Technol. 2010, 101: 6092-5). Venkata Subhash et al. used oily microorganisms to treat corncob wastewater (Bioresour.Technol., 2011, 102(19), 9286-9290). Yousuf et al. used oleaginous yeast to treat olive oil wastewater, etc. (J.Agric.Food Chem., 2010, 58(15), 8630-8635). Different from the above-mentioned fermentation wastewater, alcohol fermentation wastewater is rich in organic acids such as butyric acid and acetic acid, and the COD is often above 4000mg/L. Generally speaking, using an internal circulation anaerobic reactor (IC) and using anaerobic activated sludge to treat this fermented wastewater rich in organic acids can achieve a certain treatment effect. However, this process requires a complex internal circulation anaerobic reactor, and the construction cost is relatively high. Moreover, activated sludge needs several months of domestication to achieve the treatment effect, so the treatment efficiency is low.

目前,未见有文献或者专利报道使用油脂酵母处理醇类发酵废水。At present, there is no document or patent report on the use of oleaginous yeast to treat alcoholic fermentation wastewater.

发明内容: Invention content:

本发明的目的是提供一种能够有效处理醇类发酵废水、处理效率高、处理简便、成本低、处理时间短、发酵结束后,能够收集富含油脂、蛋白质、核酸、番茄红素等高附加值产品的酵母菌体的醇类发酵废水的处理方法。The object of the present invention is to provide a method that can effectively treat alcohol fermentation waste water, has high treatment efficiency, simple treatment, low cost, short treatment time, and can collect high-addition waste water rich in oil, protein, nucleic acid, lycopene, etc. after fermentation. A method for treating alcoholic fermentation waste water of yeast cells of value products.

本发明的醇类发酵废水的处理方法,其特征在于,包括以下步骤,去除醇类发酵废水中固型物杂质,再调节醇类发酵废水的pH值为5.0~8.0,然后按接种量为2.5~20%(v/v)接入油脂酵母种子液,发酵温度为25~35℃,发酵时间为2~5天,进行好氧发酵,发酵结束后,收集废水中的酵母菌体,废水根据排放要求进行后续处理。The method for treating alcohol fermentation wastewater of the present invention is characterized in that it comprises the following steps of removing solid impurities in alcohol fermentation wastewater, adjusting the pH value of alcohol fermentation wastewater to 5.0 to 8.0, and then adjusting the inoculum size to 2.5 ~20% (v/v) is inserted into the oil yeast seed liquid, the fermentation temperature is 25~35°C, the fermentation time is 2~5 days, and aerobic fermentation is carried out. After the fermentation, the yeast cells in the wastewater are collected. The wastewater is based on Emissions require subsequent treatment.

所述的去除醇类发酵废水中固型物杂质优选通过过滤或沉淀去除醇类发酵废水中固型物杂质。The said removal of solid impurities in the alcohol fermentation wastewater is preferably to remove the solid impurities in the alcohol fermentation wastewater by filtration or precipitation.

所述的油脂酵母可以为粘红酵母(Rhodotorula glutinis)、皮状丝孢酵母(Trichosporoncutaneum)、圆红冬孢酵母(Rhodosporidium toruloides)、斯达氏油脂酵母(Lipomyces starkeyi)、浅白隐球酵母(Cryptococcus albidus)、Trichosporon dermatis和Trichosporn coremiiforme中的任一种。Described lipozyme can be Rhodotorula glutinis, Trichosporoncutaneum, Rhodosporidium toruloides, Lipomyces starkeyi, Cryptococcus albidus ), Trichosporon dermatis and Trichosporn coremiiforme.

所述的油脂酵母种子液优选通过以下方法制备,将油脂酵母菌种接入活化培养基中,25~35℃,活化培养24~48小时,所述的活化培养基为葡萄糖或木糖20g/L、蛋白胨10g/L,酵母粉10g/L,余量为水。The described oleaginous yeast seed liquid is preferably prepared by the following method, inserting the oleaginous yeast strain into the activation medium, 25~35 ℃, activation culture for 24~48 hours, the described activation medium is glucose or xylose 20g/ L, peptone 10g/L, yeast powder 10g/L, and the balance is water.

所述的收集废水中的酵母菌体优选通过过滤或者离心收集富含油脂、蛋白、核酸、番茄红素以及其它高附加值成分的酵母菌体。The yeast cells in the collected wastewater are preferably filtered or centrifuged to collect yeast cells rich in oil, protein, nucleic acid, lycopene and other high value-added components.

本发明的有益效果如下:The beneficial effects of the present invention are as follows:

1.按照本发明的方法处理醇类发酵废水,不仅处理效率高,COD去除率高,还能免除如传统厌氧、好氧活性污泥处理方法所需的长时间菌种驯化阶段,同时生产富含油脂、蛋白、核酸、番茄红素以及其它高附加值成分的酵母菌体,具有较好的应用前景。1. According to the method of the present invention, alcohol fermentation waste water is processed, not only the treatment efficiency is high, the COD removal rate is high, but also the long-time bacteria domestication stage required by the traditional anaerobic and aerobic activated sludge treatment methods can be avoided, and the production Yeast cells rich in oil, protein, nucleic acid, lycopene and other high value-added components have good application prospects.

2.油脂酵母处理醇类废水仅需简单常规的好氧发酵设备,无需如厌氧活性污泥法等使用昂贵复杂的工艺设备(如内循环反应器等),工艺简单,成本低廉。2. Oil yeast only needs simple and conventional aerobic fermentation equipment to treat alcohol wastewater, and does not need expensive and complicated process equipment (such as internal circulation reactor, etc.) such as anaerobic activated sludge method. The process is simple and the cost is low.

3.整个发酵过程无需添加任何营养物质,发酵周期较短,产物酵母菌体收集简单。3. There is no need to add any nutrients during the whole fermentation process, the fermentation cycle is short, and the collection of product yeast cells is simple.

具体实施方式: Detailed ways:

以下实施例是对本发明的进一步说明,而不是对发明的限制。The following examples are to further illustrate the present invention, but not to limit the invention.

实施例1:Example 1:

利用粘红酵母(Rhodotorula glutinis)处理丁醇发酵废水Treatment of Butanol Fermentation Wastewater Using Rhodotorula glutinis

将粘红酵母(Rhodotorula glutinis)接入100ml的活化培养基中,25℃,活化培养48小时,得到粘红酵母种子液,所述的活化培养基为:葡萄糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Insert Rhodotorula glutinis into 100ml of activation medium, and activate and cultivate for 48 hours at 25°C to obtain Rhodotorula glutinis seed liquid. The activation medium is: glucose 20g/L, peptone 10g/L, Yeast powder 10g/L, balance is water.

将丁醇发酵废水过滤,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为25000mg/L,用乙酸调节废水的初始pH值为5.0,以10%(v/v)的接种量接入粘红酵母种子液,28℃下好氧发酵3天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过粘红酵母发酵处理后的丁醇发酵废水的COD去除率可达75%,酵母菌体量为5.5g/L。The butanol fermentation wastewater is filtered to remove solid impurities in the butanol fermentation wastewater. The initial COD of the butanol fermentation wastewater after removing impurities is about 25000mg/L, and the initial pH value of the wastewater is adjusted to 5.0 with acetic acid, with 10% ( The inoculation amount of v/v) was inserted into the seed liquid of Rhodotorula viscosum, and after aerobic fermentation at 28°C for 3 days, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subjected to subsequent treatment according to the discharge requirements. The COD removal rate of the butanol-fermented wastewater can reach 75%, and the amount of yeast cells is 5.5g/L.

实施例2Example 2

利用皮状丝孢酵母(Trichosporon cutaneum)处理丁醇发酵废水Treatment of Butanol Fermentation Wastewater by Trichosporon cutaneum

将皮状丝孢酵母(Trichosporon cutaneum)接入50ml的活化培养基中,35℃,活化培养24小时,得到皮状丝孢酵母种子液,所述的活化培养基为:木糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Insert Trichosporon cutaneum (Trichosporon cutaneum) into 50ml of activation medium, 35 DEG C, activate culture for 24 hours, obtain Trichosporon cutaneum seed liquid, described activation medium is: xylose 20g/L, Peptone 10g/L, yeast powder 10g/L, and the balance is water.

将丁醇发酵废水沉淀,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为23000mg/L,用氢氧化钙调节废水的初始pH值为8.0,以5%(v/v)的接种量接入皮状丝孢酵母种子液,28℃下好氧发酵4天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过皮状丝孢酵母发酵处理后的丁醇发酵废水的COD去除率可达80%,酵母菌体量为6.5g/L。Precipitate the butanol fermentation wastewater to remove solid impurities in the butanol fermentation wastewater. The initial COD of the butanol fermentation wastewater after removing impurities is about 23000mg/L, and the initial pH value of the wastewater is adjusted to 8.0 with calcium hydroxide. % (v/v) of the inoculum was inserted into the Trichospora dermatosus seed solution, and after 4 days of aerobic fermentation at 28°C, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subjected to subsequent treatment according to the discharge requirements. The COD removal rate of the butanol fermentation wastewater after the Trichosporium somatoides fermentation treatment can reach 80%, and the yeast cell volume is 6.5g/L.

实施例3Example 3

利用圆红冬孢酵母(Rhodosporidium toruloides)处理乙醇发酵废水Treatment of Ethanol Fermentation Wastewater Using Rhodosporidium toruloides

将圆红冬孢酵母(Rhodosporidium toruloides)接入80ml的活化培养基中,30℃,活化培养36小时,得到圆红冬孢酵母种子液,所述的活化培养基为:木糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Insert Rhodosporidium toruloides (Rhodosporidium toruloides) into 80ml of activation medium, 30 DEG C, activate culture for 36 hours, obtain Rhodosporidium toruloides seed liquid, described activation medium is: xylose 20g/L, Peptone 10g/L, yeast powder 10g/L, and the balance is water.

将丁醇发酵废水沉淀,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为12000mg/L,用氨水调节废水的初始pH值为6.5,以8%(v/v)的接种量接入圆红冬孢酵母种子液,28℃下好氧发酵2天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过圆红冬孢酵母发酵处理后的丁醇发酵废水的COD去除率可达70%,酵母菌体量为3.8g/L。The butanol fermentation wastewater is precipitated to remove solid impurities in the butanol fermentation wastewater. The initial COD of the butanol fermentation wastewater after removing impurities is about 12000mg/L, and the initial pH value of the wastewater is adjusted to 6.5 with ammonia water, with 8% ( The inoculation amount of v/v) was inserted into the seed liquid of Rhodosporidium toruloides, and after 2 days of aerobic fermentation at 28°C, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subsequently treated according to the discharge requirements. The COD removal rate of the butanol fermentation wastewater treated by the sporozoan yeast fermentation can reach 70%, and the yeast cell volume is 3.8g/L.

实施例4Example 4

利用斯达氏油脂酵母(Lipomyces starkeyi)处理乙醇发酵废水Treatment of Ethanol Fermentation Wastewater Using Lipomyces starkeyi

将斯达氏油脂酵母(Lipomyces starkeyi)接入150ml的活化培养基中,30℃,活化培养36小时,得到斯达氏油脂酵母种子液,所述的活化培养基为:木糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Lipomyces starkeyi (Lipomyces starkeyi) was inserted into the activation medium of 150ml, 30 DEG C, activated and cultivated for 36 hours to obtain the seed liquid of Lipomyces starkeyi, and the activation medium was: xylose 20g/L, Peptone 10g/L, yeast powder 10g/L, and the balance is water.

将丁醇发酵废水过滤,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为21000mg/L,用氢氧化钠调节废水的初始pH值为6.5,以20%(v/v)的接种量接入斯达氏油脂酵母种子液,30℃下好氧发酵5天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过斯达氏油脂酵母发酵处理后的丁醇发酵废水的COD去除率可达78%,酵母菌体量为4.9g/L。Filter the butanol fermentation wastewater to remove solid impurities in the butanol fermentation wastewater. The initial COD of the butanol fermentation wastewater after removing impurities is about 21000mg/L, and the initial pH value of the wastewater is adjusted to 6.5 with sodium hydroxide. % (v/v) of the inoculum was inserted into the seed liquid of Lipoyeastia studii, and after 5 days of aerobic fermentation at 30°C, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subjected to follow-up treatment according to the discharge requirements. The COD removal rate of the butanol fermentation wastewater after the fermentation treatment by L. dablii yeast can reach 78%, and the yeast cell volume is 4.9g/L.

实施例5Example 5

利用浅白隐球酵母(Cryptococcus albidus)处理丁醇发酵废水Treatment of Butanol Fermentation Wastewater by Cryptococcus albidus

将浅白隐球酵母(Cryptococcus albidus)接入125ml的活化培养基中,30℃,活化培养36小时,得到浅白隐球酵母种子液,所述的活化培养基为:木糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Insert Cryptococcus albidus into 125ml of activation medium, activate and cultivate at 30°C for 36 hours to obtain Cryptococcus albidus seed liquid, the activation medium is: xylose 20g/L, peptone 10g/L 1. Yeast powder 10g/L, and the balance is water.

将丁醇发酵废水过滤,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为24000mg/L,用氢氧化钠调节废水的初始pH值为7.5,以12%(v/v)的接种量接入浅白隐球酵母种子液,28℃下好氧发酵4天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过浅白隐球酵母发酵处理后的丁醇发酵废水的COD去除率可达65%,酵母菌体量为3.2g/L。Filter the butanol fermentation wastewater to remove solid impurities in the butanol fermentation wastewater. The initial COD of the butanol fermentation wastewater after removing impurities is about 24000mg/L, and the initial pH value of the wastewater is adjusted to 7.5 with sodium hydroxide. % (v/v) inoculum was inserted into the seed liquid of Cryptococcus albus, and after aerobic fermentation at 28°C for 4 days, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subjected to subsequent treatment according to the discharge requirements. The COD removal rate of the butanol fermentation wastewater after fermentation treatment can reach 65%, and the amount of yeast cells is 3.2g/L.

实施例6Example 6

利用Trichosporon dermatis处理乙醇发酵废水Treatment of Ethanol Fermentation Wastewater Using Trichosporon dermatis

将Trichosporon dermatis接入25ml的活化培养基中,30℃,活化培养36小时,得到Trichosporon dermatis种子液,所述的活化培养基为:葡萄糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Insert Trichosporon dermatis into 25ml of activation medium, and activate and cultivate for 36 hours at 30°C to obtain Trichosporon dermatis seed liquid. The activation medium is: glucose 20g/L, peptone 10g/L, yeast powder 10g/L, The balance is water.

将丁醇发酵废水过滤,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为18000mg/L,用氢氧化钠调节废水的初始pH值为7.8,以2.5%(v/v)的接种量接入Trichosporon dermatis种子液,25℃下好氧发酵4.5天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过Trichosporon dermatis发酵处理后的丁醇发酵废水的COD去除率可达82%,酵母菌体量为4.5g/L。The butanol fermentation wastewater is filtered to remove solid impurities in the butanol fermentation wastewater. The initial COD of the butanol fermentation wastewater after removing impurities is about 18000mg/L, and the initial pH value of the wastewater is adjusted to 7.8 with sodium hydroxide, and the pH value is adjusted to 2.5 % (v/v) inoculum was inserted into the Trichosporon dermatis seed solution, and after 4.5 days of aerobic fermentation at 25°C, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subjected to subsequent treatment according to the discharge requirements, after being fermented by Trichosporon dermatis The COD removal rate of the butanol-fermented wastewater can reach 82%, and the amount of yeast cells is 4.5g/L.

实施例7Example 7

利用Trichosporn coremiiforme处理丁醇发酵废水Treatment of Butanol Fermentation Wastewater Using Trichosporn coremiiforme

将Trichosporn coremiiforme接入80ml的活化培养基中,30℃,活化培养36小时,得到Trichosporn coremiiforme种子液,所述的活化培养基为:葡萄糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Insert Trichosporn coremiiforme into 80ml of activation medium, and activate and cultivate for 36 hours at 30°C to obtain Trichosporn coremiiforme seed liquid. The activation medium is: glucose 20g/L, peptone 10g/L, yeast powder 10g/L, The balance is water.

将丁醇发酵废水过滤,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为28000mg/L,用氢氧化钠调节废水的初始pH值为8.0,以7.5%(v/v)的接种量接入Trichosporn coremiiforme种子液,35℃下好氧发酵5天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过Trichosporn coremiiforme发酵处理后的丁醇发酵废水的COD去除率可达76%,酵母菌体量为5.1g/L。Filter the butanol fermentation wastewater to remove solid impurities in the butanol fermentation wastewater. The initial COD of the butanol fermentation wastewater after removal of impurities is about 28000mg/L, and the initial pH value of the wastewater is adjusted to 8.0 with sodium hydroxide. % (v/v) inoculum was inserted into the Trichosporn coremiiforme seed liquid, and after aerobic fermentation at 35°C for 5 days, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subjected to subsequent treatment according to the discharge requirements, after being fermented by Trichosporn coremiiforme The COD removal rate of the butanol-fermented wastewater can reach 76%, and the amount of yeast cells is 5.1g/L.

实施例8Example 8

利用Trichosporn coremiiforme处理丁醇发酵废水Treatment of Butanol Fermentation Wastewater Using Trichosporn coremiiforme

将Trichosporn coremiiforme接入80ml的活化培养基中,30℃,活化培养28小时,得到Trichosporn coremiiforme种子液,所述的活化培养基为:葡萄糖20g/L、蛋白胨10g/L、酵母粉10g/L,余量为水。Insert Trichosporn coremiiforme into 80ml of activation medium, 30°C, activate and cultivate for 28 hours to obtain Trichosporn coremiiforme seed liquid, the activation medium is: glucose 20g/L, peptone 10g/L, yeast powder 10g/L, The balance is water.

将丁醇发酵废水过滤,去除丁醇发酵废水中固型物杂质,去除杂质后的丁醇发酵废水起始COD约为4000mg/L,用氢氧化钠调节废水的初始pH值为6.5,以20%(v/v)的接种量接入Trichosporn coremiiforme种子液,30℃下好氧发酵5天后,离心收集丁醇发酵废水中的酵母菌体,废水根据排放要求进行后续处理,经过Trichosporn coremiiforme发酵处理后的丁醇发酵废水的COD去除率可达80%,酵母菌体量为0.81g/L。Butanol fermentation wastewater is filtered to remove solid impurities in butanol fermentation wastewater. The initial COD of butanol fermentation wastewater after removing impurities is about 4000mg/L, and the initial pH value of wastewater is adjusted to 6.5 with sodium hydroxide. % (v/v) inoculum was inserted into the Trichosporn coremiiforme seed liquid, and after aerobic fermentation at 30°C for 5 days, the yeast cells in the butanol fermentation wastewater were collected by centrifugation, and the wastewater was subjected to subsequent treatment according to the discharge requirements, after being fermented by Trichosporn coremiiforme The COD removal rate of the butanol-fermented wastewater can reach 80%, and the amount of yeast cells is 0.81g/L.

Claims (4)

1. the treatment process of an alcohols fermentation waste water, it is characterized in that, comprise the following steps, remove solid impurity in the alcohols fermentation waste water, the pH value of regulating again the alcohols fermentation waste water is 5.0~8.0, then by inoculum size, be volume ratio 2.5~20% access saccharomyces oleaginosus seed liquor, leavening temperature is 25~35 ℃, and fermentation time is 2~5 days, carry out aerobic fermentation, after fermentation ends, collect the yeast thalline in waste water, waste water carries out subsequent disposal according to emission request;
Described saccharomyces oleaginosus is any in rhodotorula glutinis (Rhodotorula glutinis), trichosporon cutaneum (Trichosporon cutaneum), circle red winter spore yeast (Rhodosporidium toruloides), Lipomyces starkeyi (Lipomyces starkeyi), light white latent ball yeast (Cryptococcus albidus), Trichosporon dermatis and Trichosporn coremiiforme.
2. the treatment process of alcohols fermentation waste water according to claim 1, is characterized in that, in described removal alcohols fermentation waste water, solid impurity is to remove solid impurity in the alcohols fermentation waste water by filtering or precipitating.
3. the treatment process of alcohols fermentation waste water according to claim 1, it is characterized in that, described saccharomyces oleaginosus seed liquor is to prepare by the following method, by in saccharomyces oleaginosus bacterial classification access activation medium, 25~35 ℃, activation culture 24~48 hours, described activation medium is glucose or wood sugar 20g/L, peptone 10g/L, yeast powder 10g/L, surplus is water.
4. the treatment process of alcohols fermentation waste water according to claim 1, is characterized in that, the yeast thalline in described collection waste water is by filtering or centrifugal collection.
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