JP2000271589A - Method for treating oil-containing drainage by activated sludge and culture medium for propagating bacteria for treating oil-containing drainage - Google Patents
Method for treating oil-containing drainage by activated sludge and culture medium for propagating bacteria for treating oil-containing drainageInfo
- Publication number
- JP2000271589A JP2000271589A JP7905499A JP7905499A JP2000271589A JP 2000271589 A JP2000271589 A JP 2000271589A JP 7905499 A JP7905499 A JP 7905499A JP 7905499 A JP7905499 A JP 7905499A JP 2000271589 A JP2000271589 A JP 2000271589A
- Authority
- JP
- Japan
- Prior art keywords
- treatment
- oil
- wastewater
- drainage
- sub
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000010802 sludge Substances 0.000 title claims abstract description 48
- 238000000034 method Methods 0.000 title claims description 33
- 239000001963 growth medium Substances 0.000 title claims description 13
- 241000894006 Bacteria Species 0.000 title description 28
- 230000001902 propagating effect Effects 0.000 title 1
- 239000003921 oil Substances 0.000 claims abstract description 38
- 244000005700 microbiome Species 0.000 claims abstract description 22
- 239000010730 cutting oil Substances 0.000 claims abstract description 21
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- 239000001301 oxygen Substances 0.000 claims abstract description 5
- 239000002351 wastewater Substances 0.000 claims description 58
- 239000002609 medium Substances 0.000 claims description 30
- 235000013379 molasses Nutrition 0.000 claims description 11
- 239000001888 Peptone Substances 0.000 claims description 9
- 108010080698 Peptones Proteins 0.000 claims description 9
- 235000019319 peptone Nutrition 0.000 claims description 9
- 108010009004 proteose-peptone Proteins 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 7
- 238000012545 processing Methods 0.000 claims description 6
- 244000068988 Glycine max Species 0.000 claims description 5
- 235000010469 Glycine max Nutrition 0.000 claims description 5
- 238000004065 wastewater treatment Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 238000003672 processing method Methods 0.000 claims description 3
- 241000233866 Fungi Species 0.000 claims 1
- 238000011282 treatment Methods 0.000 abstract description 56
- 239000007788 liquid Substances 0.000 abstract description 5
- 230000000644 propagated effect Effects 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 description 33
- 230000001580 bacterial effect Effects 0.000 description 9
- 230000000813 microbial effect Effects 0.000 description 9
- 230000008859 change Effects 0.000 description 7
- AIUDWMLXCFRVDR-UHFFFAOYSA-N dimethyl 2-(3-ethyl-3-methylpentyl)propanedioate Chemical compound CCC(C)(CC)CCC(C(=O)OC)C(=O)OC AIUDWMLXCFRVDR-UHFFFAOYSA-N 0.000 description 7
- 239000002035 hexane extract Substances 0.000 description 7
- 238000005273 aeration Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 239000000306 component Substances 0.000 description 5
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229930006000 Sucrose Natural products 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 238000012258 culturing Methods 0.000 description 4
- 239000012533 medium component Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000035939 shock Effects 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000003213 activating effect Effects 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000005188 flotation Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- -1 for example Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000036284 oxygen consumption Effects 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 1
- 108010023063 Bacto-peptone Proteins 0.000 description 1
- 206010052804 Drug tolerance Diseases 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000122973 Stenotrophomonas maltophilia Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 241001148470 aerobic bacillus Species 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 229940041514 candida albicans extract Drugs 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 238000012136 culture method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
- 230000036425 denaturation Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000026781 habituation Effects 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000013028 medium composition Substances 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000013630 prepared media Substances 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 241001148471 unidentified anaerobic bacterium Species 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
Classifications
-
- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/10—Biological treatment of water, waste water, or sewage
Landscapes
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Activated Sludge Processes (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、水溶性切削油を大
量に含む含油排水を回分式活性汚泥法によって処理する
方法に関する。さらに、本発明は、含油排水を活性汚泥
法で処理するために菌を投入する処理方法による、前処
理における菌の増殖用培地に関する。The present invention relates to a method for treating oil-containing wastewater containing a large amount of water-soluble cutting oil by a batch activated sludge method. Furthermore, the present invention relates to a culture medium for growing bacteria in pretreatment by a treatment method in which bacteria are introduced to treat oil-containing wastewater by the activated sludge method.
【0002】[0002]
【従来の技術】従来より、含油排水の処理は、油分(ヘ
キサン抽出物、例えば切削油)の影響が大きく、一般的
な活性汚泥中における微生物が生存するのは困難であ
る。したがって、活性汚泥法による微生物処理を含油排
水に対して行うのは難しく、加圧浮上槽での凝集剤添加
等による物理的・化学的処理が行われている。その中で
も、切削油を含む含油排水の微生物による処理は、困難
であることが知られている。2. Description of the Related Art Conventionally, the treatment of oil-containing wastewater is greatly affected by oil (hexane extract, for example, cutting oil), and it is difficult for microorganisms to survive in general activated sludge. Therefore, it is difficult to perform microbial treatment by an activated sludge method on oil-containing wastewater, and physical and chemical treatments such as the addition of a flocculant in a pressurized flotation tank are performed. Among them, it is known that treatment of oil-containing wastewater containing cutting oil with microorganisms is difficult.
【0003】最近、酵母による含油排水の処理方法が発
表されたが、食品工場等から排出される動植物性の油に
ついてのものであった。さらに、一次処理として、酵母
専用の曝気槽及び沈殿槽、二次処理としての通常の活性
汚泥法の曝気槽及び沈殿槽を設置したものであった。[0003] Recently, a method of treating oil-containing wastewater with yeast has been announced, but it concerns animal and vegetable oils discharged from food factories and the like. Further, as the primary treatment, an aeration tank and a sedimentation tank dedicated to yeast were installed, and as a secondary treatment, an aeration tank and a sedimentation tank of a usual activated sludge method were installed.
【0004】特開平9−75075号公報には、細菌で
あるステノトロホモナス・マルトフィリアを好気条件下
で含油排水と接触させて、特に動植物油を含有する厨房
排水の処理に用いる方法が開示されている。Japanese Patent Application Laid-Open No. 9-75075 discloses a method in which a bacterium, Stenotrophomonas maltophilia, is brought into contact with oil-containing wastewater under aerobic conditions, and particularly used for treating kitchen wastewater containing animal and vegetable oils. Have been.
【0005】[0005]
【発明が解決しようとする課題】上述のように切削油を
含む排水は特殊であるため、市販の活性汚泥法用の菌を
投入しても種汚泥は死滅する。通常の馴養方法では、種
汚泥中の微生物を生存させておくことができない。ま
た、この含油排水から通常実験用細菌培地(一般細菌培
地など)を用いた集積培養では、種汚泥中の油分解性が
ある特殊な菌を馴養させることができなかった。従来行
われているような凝集剤添加等による物理的・化学的処
理のための施設は、かなり大型となり、薬品にかかる費
用も大きい。As described above, since the wastewater containing cutting oil is special, even if bacteria for the activated sludge method commercially available are introduced, the seed sludge will die. The usual habituation method cannot keep the microorganisms in the seed sludge alive. In addition, in the enrichment culture using a bacterial culture medium for ordinary experiments (such as a general bacterial culture medium) from the oil-containing wastewater, it was not possible to acclimate special oil-degrading bacteria in the seed sludge. A conventional facility for physical and chemical treatment by adding a coagulant or the like becomes considerably large, and the cost for chemicals is large.
【0006】特に、工場から排出される切削油を大量に
含む排水は、エマルジョン化していて、さらに界面活性
剤が大量に含まれるため、水相部分が嫌気状態になり、
活性汚泥法に用いるための微生物の生存、増殖がより困
難である。また、切削排水を希釈して油分濃度を低下さ
せて微生物により処理することも可能ではあるが、希釈
により処理排水量が増加し、希釈設備がさらに要求さ
れ、コスト増につながるため、原排水のままで処理する
ことが望まれる。したがって、本発明は、従来、処理の
困難であった含油排水を活性汚泥処理するための微生物
増殖用培地、及び、当該排水の活性汚泥処理方法を開発
することを目的とする。In particular, wastewater containing a large amount of cutting oil discharged from a factory is emulsified and contains a large amount of a surfactant, so that the aqueous phase becomes anaerobic,
It is more difficult for microorganisms to survive and proliferate for use in the activated sludge method. It is also possible to dilute the cutting wastewater to reduce the oil concentration and treat it with microorganisms.However, dilution increases the amount of treated wastewater, further requires dilution equipment, and increases costs. It is desired to process with. Accordingly, an object of the present invention is to develop a microorganism growth medium for treating activated oil-containing wastewater, which has been conventionally difficult to treat, with an activated sludge, and an activated sludge treatment method for the wastewater.
【0007】[0007]
【課題を解決するための手段】本発明は、切削油を大量
に含む含油排水を活性汚泥法で処理するものである。切
削油を分解する微生物は、その増殖培地及び培養方法が
確立されていないという点で特殊であり、種汚泥が油分
によるショックで死滅するため、通常の馴養が困難であ
る。通常の馴養方法では、馴養開始7日以内で静置時に
水面に浮いた状態となり、種汚泥が死滅する。したがっ
て、含油排水から切削油を処理できる混合微生物集団
を、集積培養し、増殖させ、添加することとした。ま
た、集積培養においては、本発明の培地を用いて、切削
油を処理できる微生物の増殖を行うことができる。SUMMARY OF THE INVENTION The present invention treats oil-containing wastewater containing a large amount of cutting oil by an activated sludge method. Microorganisms that decompose cutting oil are special in that their growth medium and culture method have not been established, and seed sludge is killed by shock due to oil content, so that normal acclimation is difficult. In a normal acclimatization method, the seed sludge is killed within 7 days from the start of acclimation and floats on the water surface at rest. Therefore, a mixed microbial population capable of treating cutting oil from the oil-containing wastewater is to be cultured, grown, and added. In addition, in the enrichment culture, microorganisms capable of treating cutting oil can be grown using the medium of the present invention.
【0008】本発明は、切削油排水中の混合微生物集団
を集積培養し、培養された混合微生物集団を排水流入時
に添加することを特徴とする回分式活性汚泥法による含
油排水の活性汚泥による処理方法を提供する。ここで、
本処理方法において、亜嫌気状態、好気状態、嫌気状態
とする処理サイクルを順に繰り返すのが好ましい。ま
た、上記亜嫌気状態は、溶存酸素が約0.5mg/L以
下であるが、0mg/Lではない条件であって、この亜
嫌気状態の間に撹拌するのが好ましい。[0008] The present invention provides a method for treating oil-containing wastewater with activated sludge by a batch-type activated sludge method, wherein a mixed microorganism group in cutting oil wastewater is accumulated and cultured, and the cultured mixed microorganism group is added when the wastewater flows into the wastewater. Provide a way. here,
In the present processing method, it is preferable to repeat a processing cycle of sub-anaerobic state, aerobic state, and anaerobic state in order. In the sub-anaerobic state, the dissolved oxygen is about 0.5 mg / L or less, but not 0 mg / L, and it is preferable to stir during the sub-anaerobic state.
【0009】本発明における含油排水処理菌用の増殖用
培地としては、処理すべき含油排水と、窒素源としてカ
ゼイン製ペプトン及び大豆ペプトンと、炭素原として糖
蜜とを含むものである。[0009] The growth medium for the oil-containing wastewater treatment bacteria in the present invention contains oil-containing wastewater to be treated, casein peptone and soybean peptone as a nitrogen source, and molasses as a carbon source.
【0010】[0010]
【発明の実施の形態】本発明の培地は、一般細菌用培地
成分と比べて、カゼイン製ペプトン、大豆ペプトンをと
もに添加する点、ショ糖の代わりに糖蜜を添加する点、
オートクレーブ処理した排水を添加する点において主と
して特徴がある。なお、一般細菌用培地は、ペプトン5
g/L、酵母エキス2.5g/L、ブドウ糖1g/L、
pH7.0のものが従来から知られている。BEST MODE FOR CARRYING OUT THE INVENTION The medium of the present invention is characterized in that casein peptone and soybean peptone are added together, and molasses is added in place of sucrose, as compared with general bacterial medium components.
It is characterized mainly by the addition of autoclaved wastewater. The culture medium for general bacteria is Peptone 5
g / L, yeast extract 2.5 g / L, glucose 1 g / L,
Those having a pH of 7.0 are conventionally known.
【0011】本発明の培地は、窒素源として、カゼイン
製ペプトンと大豆ペプトンをともに含むものである。大
豆ペプトンは、微生物の培養、特に発育困難な菌の培養
に適している。大豆ペプトンの添加により、切削油を含
む排水を処理する能力を有し、含油排水中で生育可能な
混合微生物集団を増殖させることができる。例えば、カ
ゼイン製ペプトンと大豆ペプトンの合計で約10〜30
g/L、好ましくは約14〜25g/L含むものであっ
て、そのうち、カゼイン製ペプトンを約8〜25g/
L、好ましくは約13〜20g/L、大豆ペプトンを約
0.5〜6g/L、好ましくは約1〜5g/L含むもの
がよい。カゼイン製ペプトンのみ、又は大豆ペプトンの
みを含む培地では、増殖率が悪く、好ましくない。The medium of the present invention contains both casein peptone and soybean peptone as nitrogen sources. Soy peptone is suitable for culturing microorganisms, particularly for culturing difficult-to-grow bacteria. By the addition of soy peptone, a mixed microbial population capable of processing wastewater containing cutting oil and capable of growing in the oil-containing wastewater can be grown. For example, casein peptone and soy peptone in total are about 10-30
g / L, preferably about 14-25 g / L, of which casein peptone is about 8-25 g / L.
L, preferably about 13-20 g / L, and about 0.5-6 g / L, preferably about 1-5 g / L of soy peptone. A medium containing only casein-made peptone or only soybean peptone is not preferable because the growth rate is poor.
【0012】また、本発明の培地は、炭素原として、糖
蜜を約4〜12ml/L(約0.03〜0.1%)程
度、好ましくは約8〜10ml/L添加する。通常の培
地では、ショ糖を使用するが、活性汚泥による排水処理
では、糖蜜は、バルキングなど汚泥状態が悪化した場
合、添加する場合が多く、汚泥との相性がよいため、好
ましい。さらに、糖蜜は、ショ糖に比べ、雑菌の繁殖を
抑える一方、本発明に有用な綿状の菌(未同定)など、
本発明の方法に有効な特殊かつ特徴的な菌を増殖させる
ことが可能となる。糖蜜を0.1%以上加えると菌の増
殖が低下する。In the medium of the present invention, molasses is added as a carbon source in an amount of about 4 to 12 ml / L (about 0.03 to 0.1%), preferably about 8 to 10 ml / L. In a normal medium, sucrose is used, but in the wastewater treatment with activated sludge, molasses is often added when the state of sludge such as bulking deteriorates, and it is preferable because it is compatible with sludge. In addition, molasses suppresses the growth of various bacteria compared to sucrose, while flocculent bacteria (unidentified) useful in the present invention,
It is possible to grow special and characteristic bacteria effective for the method of the present invention. When molasses is added in an amount of 0.1% or more, the growth of bacteria is reduced.
【0013】なお、他の培地成分として、リン酸二水素
カリウム、塩化ナトリウム等の無機塩類を添加する。そ
れぞれの添加量は、例えば、約2〜10g/L、好まし
くは約3〜8g/L、さらに好ましくは約5g/L程度
である。[0013] As other medium components, inorganic salts such as potassium dihydrogen phosphate and sodium chloride are added. The amount of each addition is, for example, about 2 to 10 g / L, preferably about 3 to 8 g / L, and more preferably about 5 g / L.
【0014】本培地は、オートクレーブで予め滅菌処理
した排水成分を添加する。排水成分のオートクレーブに
よる前処理は、通常のオートクレーブ処理に用いる12
1℃よりやや低い温度で、やや長時間かけて行う。オー
トクレーブ処理は、好ましくは、約110〜約118℃
で約10〜50分程度、より好ましくは25〜40分程
度で行うことができる。通常のオートクレーブ処理に用
いる121℃より低い温度設定としたのは、高温による
排水中のタンパク質の分解による変性を防ぐためであ
る。The medium is supplemented with a wastewater component which has been sterilized in an autoclave in advance. The pretreatment of the wastewater component by autoclave is performed by using the usual autoclave treatment.
It is carried out at a temperature slightly lower than 1 ° C. and for a slightly longer time. The autoclaving is preferably performed at about 110 to about 118 ° C.
About 10 to 50 minutes, more preferably about 25 to 40 minutes. The temperature was set lower than 121 ° C., which is used for normal autoclave treatment, in order to prevent denaturation due to decomposition of proteins in wastewater due to high temperature.
【0015】オートクレーブ処理した含油排水を、培地
に約50〜170ml/L、好ましくは約80〜120
ml/L添加するのが好ましいが、排水成分は日によっ
て変動するため、それに応じて添加量を適宜変更する。
なお、通常、50ml/Lより少ない量だと、菌相が変
わり、170ml/Lより多量添加すると切削油の影響
が強く、増殖力が低下するため、好ましくない。但し、
排水成分によっては、これらの範囲以上又は以下の量を
添加することもできる。The autoclaved oil-containing wastewater is added to the medium at about 50 to 170 ml / L, preferably about 80 to 120 ml / L.
It is preferable to add ml / L, but since the wastewater component varies from day to day, the addition amount is appropriately changed accordingly.
In general, if the amount is less than 50 ml / L, the bacterial flora changes. If the amount is more than 170 ml / L, the influence of the cutting oil is strong, and the proliferation power is undesirably reduced. However,
Depending on the drainage component, an amount not less than or more than these ranges can be added.
【0016】培地調整後、さらに、上述のオートクレー
ブ条件で、培地を滅菌する。本培地のpHは、汚泥に添
加したときに、汚泥とのpHの違いによるショックによ
る死滅を防ぐため、培地調整後のオートクレーブ処理し
た培地のpHが6.8〜7.5程度となるようにする。
このpH値では、一般細菌が増殖しやすいため、市販の
活性汚泥法用の菌などでは、pHが高すぎるとされ、p
Hを下げる処置をするが、本発明の培地では、培地中に
排水成分及び糖蜜を含むため、他の一般細菌が増殖しに
くい環境下にある。したがって、pH6.8〜7.5程
度での培養が可能となる。なお、オートクレーブ後のp
Hがこの値からはずれる場合は、適宜、適当な酸又はア
ルカリ、例えばHClやNaOHによって、調製する。After adjusting the medium, the medium is further sterilized under the above-mentioned autoclave conditions. The pH of the medium is adjusted so that when added to the sludge, the pH of the autoclaved medium after the medium adjustment is about 6.8 to 7.5 to prevent death due to shock due to the difference in pH from the sludge. I do.
At this pH value, general bacteria are easy to grow, so that it is considered that the pH is too high for bacteria for a commercial activated sludge method and the like.
Although the treatment for lowering H is performed, the medium of the present invention is in an environment where other general bacteria are unlikely to grow because the medium contains drainage components and molasses. Therefore, culture at a pH of about 6.8 to 7.5 becomes possible. In addition, p after autoclave
If H deviates from this value, it is prepared as appropriate with a suitable acid or alkali, such as HCl or NaOH.
【0017】本発明の培地として、下記の表のような培
地組成のものがあげられるが、一例であって、これに限
られるものではない。The medium of the present invention may have a medium composition as shown in the following table, but is by way of example and not limited thereto.
【0018】[0018]
【表1】 [Table 1]
【0019】切削油排水処理菌の増殖方法を次に示す。
排水もしくは集積培養した混合微生物集団を、調整後の
培地(液体)に約0.1〜3%(v/v)、好ましく
は、約1%(v/v)の割合で無菌的に添加する。継代
培養も同じ割合で行う。培養菌は、1%の添加で24〜
48時間後には増殖が平衡に達し、その後増殖率は減少
する。そのため、24〜48時間以前に活性汚泥への添
加を行うのが望ましい。10回程度の継代では、菌相に
変化は生じない。The method of multiplying the cutting oil wastewater treatment bacteria will be described below.
The mixed microorganism population drained or accumulated is aseptically added to the adjusted medium (liquid) at a rate of about 0.1 to 3% (v / v), preferably about 1% (v / v). . Subculture is performed at the same ratio. The culture is 24 ~
After 48 hours, growth reaches equilibrium, after which the growth rate decreases. Therefore, it is desirable to add to activated sludge before 24-48 hours. After about 10 passages, no change occurs in the bacterial flora.
【0020】培養温度は、30〜37℃で100rpm
以下で振盪培養する。前記範囲外では、増殖速度が遅
く、また、菌相に変化が生じることもあるため、好まし
くない。また、使用した排水の濃度によって異なるが、
静置培養した場合は、増殖速度が遅く、培地成分の糖蜜
が沈殿する傾向があり、通常の界面活性剤濃度では、1
00rpmより早い振盪で培養すると、培地が泡だっ
て、局所的に嫌気状態となるので好ましくない。振盪の
程度は、排水中の界面活性剤の濃度に応じて変更すべき
ものである。活性汚泥への培養液の添加量は、処理槽中
の総量の約0.01〜1%(v/v)、好ましくは約
0.1%(v/v)である。The culture temperature is 100 rpm at 30 to 37 ° C.
Shake culture below. Outside the above range, the growth rate is low and the bacterial flora sometimes changes. It also depends on the concentration of wastewater used,
In the case of stationary culture, the growth rate is low, and molasses as a medium component tends to precipitate.
Culturing with shaking at a speed higher than 00 rpm is not preferable because the medium becomes bubbles and becomes locally anaerobic. The degree of shaking should be changed according to the concentration of the surfactant in the waste water. The amount of the culture solution added to the activated sludge is about 0.01 to 1% (v / v), preferably about 0.1% (v / v) of the total amount in the treatment tank.
【0021】処理すべき含油排水は、処理工程におい
て、順に亜嫌気状態、好気状態、嫌気状態の3つの状態
のサイクルとする。このサイクルは、約15〜30時
間、好ましくは、約24時間とすることがことができ
る。本発明では、混合微生物集団の汚泥中での充分な滞
留時間をとり、比較的増殖速度の低い生物を含む場合で
あっても、定着、増殖が安定化し、かつ、亜嫌気状態が
維持できるといった利点のある回分培養を行うのが好適
である。本発明による回分培養の例を、図1に示す。The oil-containing wastewater to be treated is cycled in the treatment step into three states: a sub-anaerobic state, an aerobic state, and an anaerobic state. This cycle can be about 15-30 hours, preferably about 24 hours. In the present invention, a sufficient residence time of the mixed microbial population in the sludge is ensured, and even in the case of including organisms having a relatively low growth rate, the fixation and growth are stabilized, and the subanaerobic state can be maintained. It is preferred to carry out batch culture with advantages. FIG. 1 shows an example of batch culture according to the present invention.
【0022】亜嫌気処理前に、亜嫌気処理の前に添加す
る活性化液(汚泥)を準備すべく、混合微生物集団を含
油排水から集積培養して、増殖させた後、汚泥中に添加
して排水処理用の活性汚泥を作成する。このときの集積
培養及びその培養に用いる培地としては、本発明の培地
を用いるのが微生物がよく増殖する点で好ましい。Before the sub-anaerobic treatment, in order to prepare an activating solution (sludge) to be added before the sub-anaerobic treatment, the mixed microbial population is accumulated and cultured from the oil-containing wastewater, grown, and then added to the sludge. To produce activated sludge for wastewater treatment. At this time, it is preferable to use the medium of the present invention as the medium for the enrichment culture and the culture in that the microorganisms grow well.
【0023】処理すべき排水を処理槽に注入し、処理槽
には必要に応じて、活性化液を更に添加する。活性化液
の処理槽への注入は、各サイクル毎ないしは7日に1回
の割合で行うものであるが、好ましくは各サイクル毎に
行うのがよい。まず、亜嫌気状態にして、排水と汚泥を
分離させないように撹拌のみを行う。撹拌しないと、油
分により汚泥分が浮き上がってきてしまうため、好まし
くない。なお、この撹拌は、泡立たない程度にゆっくり
行う。なお、ここで、好気処理(典型的には、DO(溶
存酸素)が1.5〜3.mg/L)あるいは、これ以上
の過曝気では、フロックが分散して、沈殿物が増大し
て、沈殿しなくなるため、好ましくない。The wastewater to be treated is poured into a treatment tank, and an activating liquid is further added to the treatment tank as needed. The activation liquid is injected into the treatment tank every cycle or once every seven days, but is preferably performed every cycle. First, the mixture is placed in a sub-anaerobic state, and only stirring is performed so as not to separate drainage and sludge. If the stirring is not performed, the sludge is lifted by the oil, which is not preferable. This stirring is performed slowly so as not to cause foaming. Here, in the aerobic treatment (typically, DO (dissolved oxygen) is 1.5 to 3. mg / L) or in excess aeration, flocs are dispersed and precipitates increase. Therefore, it is not preferable because precipitation does not occur.
【0024】亜嫌気処理とは、一般にDO(溶存酸素)
が0mg/Lとはならないが、DOを極めて低い状態に
することをいう。例えば、DOを約0.8mg/L以
下、好ましくは、約0.5mg/L以下とすることをい
う。特に、ここでの亜嫌気処理は、DOが約0.8mg
/L以下、好ましくは、DOが約0.5mg/L以下で
あって、0mg/Lでない条件とする。添加する混合微
生物集団は亜嫌気培養条件下で増殖するため、嫌気条件
下(0mg/L)では増殖及び分解処理ができないため
である。一方、水溶性切削油を大量に含む含油排水は、
界面活性剤が大量に含まれるため、亜嫌気処理を行わず
に曝気処理を行うと、泡立ってしまい、泡により空気に
触れない部分が生じ、好ましくない。この亜嫌気処理に
より、SS(懸濁物質)、ヘキサン抽出物の処理が特に
好適に進む。The sub-anaerobic treatment generally means DO (dissolved oxygen)
Does not become 0 mg / L, but refers to bringing DO to an extremely low state. For example, it means that DO is set to about 0.8 mg / L or less, preferably about 0.5 mg / L or less. In particular, the sub-anaerobic treatment here is about 0.8 mg of DO.
/ L or less, preferably DO is about 0.5 mg / L or less and not 0 mg / L. This is because the mixed microorganism population to be added grows under sub-anaerobic culture conditions, and cannot be grown and decomposed under anaerobic conditions (0 mg / L). On the other hand, oil-containing wastewater containing a large amount of water-soluble cutting oil
Since the surfactant is contained in a large amount, if the aeration treatment is performed without performing the sub-anaerobic treatment, bubbles are formed, and a portion that does not come into contact with air is generated by the bubbles, which is not preferable. By this sub-anaerobic treatment, the treatment of the SS (suspended matter) and hexane extract proceeds particularly suitably.
【0025】亜嫌気処理の時間は、約15〜60分程度
で、好ましくは、約30〜40分程度行う。亜嫌気処理
時間が15分より短いと、処理が不十分であり、60分
よりも長時間の処理を行っても、処理結果に差が生じな
いため、経済的でない。The subanaerobic treatment time is about 15 to 60 minutes, preferably about 30 to 40 minutes. If the sub-anaerobic treatment time is shorter than 15 minutes, the treatment is insufficient, and even if the treatment is carried out for longer than 60 minutes, there is no difference in the treatment result, which is not economical.
【0026】亜嫌気処理の後、DOが平均1.5mg/
L程度の好気条件となるよう曝気処理を行う。なお、好
気的条件は、DOが0.8以上、フロックの分散が生じ
ない約3.0mg/L以下のDOに保つのが望ましい。
また、曝気せずに撹拌により同様なDOを達成すること
も可能である。この好気処理は、約15〜30時間程度
行う。好気処理時間が15時間より短いと、処理が不十
分であり、30時間より長くても処理結果に差が生じな
いため、経済的でない。なお、好ましくは22時間程度
である。After the sub-anaerobic treatment, the DO averaged 1.5 mg /
The aeration process is performed so that the aerobic condition is about L. The aerobic conditions are desirably maintained at a DO of 0.8 or more and a DO of about 3.0 mg / L or less at which floc dispersion does not occur.
It is also possible to achieve a similar DO by stirring without aeration. This aerobic treatment is performed for about 15 to 30 hours. If the aerobic treatment time is shorter than 15 hours, the treatment is insufficient, and if the aerobic treatment time is longer than 30 hours, there is no difference in the treatment result, so that it is not economical. In addition, it is preferably about 22 hours.
【0027】好気処理を行った後、0.5〜2時間程度
の嫌気処理を行う。この嫌気処理により、好気性の菌か
ら、亜嫌気性の菌相に変化していく。最終的には、処理
液のDOは、ゼロに近づく。なお、この処理において、
嫌気性の菌は、増殖が遅いため、嫌気性菌が優占するこ
とはない。したがって、処理時に腐敗が起こることはな
く、悪臭の発生がないという利点がある。After the aerobic treatment, the anaerobic treatment is performed for about 0.5 to 2 hours. By this anaerobic treatment, the bacteria change from aerobic bacteria to a subanaerobic flora. Eventually, the DO of the processing solution approaches zero. In this process,
Anaerobic bacteria do not dominate because of slow growth. Therefore, there is an advantage that no rot occurs during the treatment and no odor is generated.
【0028】切削油の排水は、上述したように、油分濃
度が高いため、菌の増殖において好ましくないが、原排
水のままで処理することが望まれ、本発明はそれを可能
にするものである。しかしながら、本発明の方法によれ
ば、排水を適当な濃度で希釈したものを処理することも
可能である。As described above, the drainage of cutting oil has a high oil content, which is not preferable for the growth of bacteria. However, it is desired to treat the raw wastewater as it is, and the present invention makes it possible. is there. However, according to the method of the present invention, it is also possible to treat wastewater diluted to an appropriate concentration.
【0029】[0029]
【実施例】以下に実施例を挙げて、本発明をさらに詳細
に説明するが、これらにより本発明を制限するものでは
ない。EXAMPLES The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the present invention is limited thereto.
【0030】切削油を含む含油排水処理用細菌の増殖培
地 使用した培地を以下の表に示す。培地成分に含まれるペ
プトンについては、カゼイン製ペプトンはDEFCO
BACTO PEPTONE(タンパク質の酵素消化
物)、大豆ペプトンは日本製薬製のポリペプトンSを用
いた。The following table shows the culture medium used for the growth medium of the bacteria for treating oil-containing wastewater containing cutting oil. Regarding the peptone contained in the medium components, casein peptone is DEFCO
As BACTO PEPTONE (enzyme digest of protein) and soy peptone, Nippon Pharmaceutical's polypeptone S was used.
【0031】[0031]
【表2】 [Table 2]
【0032】用いた含油排水は、スズキ株式会社の本社
工場(静岡県浜松市)の含油排水を用いた。スズキ株式
会社の本社工場の含油排水は、機械加工工程の排水であ
り、生活用水ではない。実験に使用する日の朝10時3
0分ころに工場より採取した。以下のpH、組成等を有
する。表中の値は平均値である。含油排水は、115℃
で30分間オートクレーブ処理した。表3において、B
ODは、生物化学的酸素消費量を、CODは化学的酸素
消費量を、T−Nは全窒素量を、T−Pは全リン量をそ
れぞれ表す。The oil-containing wastewater used was the oil-containing wastewater from the headquarters factory of Suzuki Motor Corporation (Hamamatsu City, Shizuoka Prefecture). The oil-containing wastewater at the Suzuki headquarters factory is wastewater from the machining process, not domestic water. 10:03 in the morning on the day of the experiment
At about 0 minutes, it was collected from the factory. It has the following pH, composition, etc. The values in the table are average values. Oil-impregnated wastewater at 115 ° C
For 30 minutes. In Table 3, B
OD indicates biochemical oxygen consumption, COD indicates chemical oxygen consumption, TN indicates total nitrogen amount, and TP indicates total phosphorus amount.
【0033】[0033]
【表3】 [Table 3]
【0034】集積培養した混合微生物集団を調整後の上
記培地に約1%(v/v)添加し、回分式の培養を行っ
た。その結果、微生物は増殖し、増加した微生物を汚泥
中に添加することにより、混合微生物集団の汚泥におけ
る安定的な定着、増殖が得られた。About 1% (v / v) of the mixed microbial population that had been enriched and cultured was added to the above-prepared medium, and batch culture was performed. As a result, the microorganisms proliferated, and by adding the increased microorganisms to the sludge, stable establishment and growth of the mixed microbial population in the sludge were obtained.
【0035】増殖培地におけるペプトンの組成が微生物
の増殖に与える影響 上記した本発明の培地のカゼイン製ペプトン17g/L
と大豆ペプトン3g/Lの代わりに、カゼイン製ペプト
ンのみ20g/Lを用いた培地と、大豆ペプトンのみ2
0g/Lを用いた培地について同様な実験を行ったとこ
ろ、本発明の培地を用いた場合よりも、菌数が少なく、
増殖率が低かった。結果を表4に示す。Influence of the composition of peptone in the growth medium on the growth of microorganisms The casein peptone 17 g / L of the medium of the present invention described above.
Medium containing only 20 g / L of casein peptone instead of 3 g / L of soy peptone and 2 g of soy peptone only
When a similar experiment was performed on a medium using 0 g / L, the number of bacteria was smaller than when the medium of the present invention was used.
The growth rate was low. Table 4 shows the results.
【0036】[0036]
【表4】 [Table 4]
【0037】増殖培地における糖蜜が微生物の増殖に与
える影響 上記培地に1.5%寒天を加え、リン酸塩緩衝液(pH
7.2)を希釈水として用いた1mLの希釈含有排水を
混釈培養した。リン酸塩緩衝液は、JIS K0102
の72.2に従って調節した。培養は、36℃で1時間
の80rpmの旋回による振盪培養により行い、培養
後、プレートに蒔いて観察したところ、菌数、コロニー
数、菌種とも含油排水の処理に用いるのに十分な程度に
増加が見られた。一方、糖蜜の代わりに同濃度のショ糖
を培地に添加した培地を用いた場合は、油の分解を行わ
ない一般細菌の繁殖が見られ、菌数、コロニー数、菌種
とも、糖蜜を用いたときほど増殖しなかった。また、一
般細菌の培地(標準培地)を使用した場合、菌数、コロ
ニー数、菌種とも少なく、コロニーの発達が極度に悪か
った。Effect of molasses on growth of microorganism in growth medium 1.5% agar was added to the above medium, and phosphate buffer (pH
1 mL of dilution-containing wastewater using 7.2) as dilution water was pour-cultured. The phosphate buffer is JIS K0102
72.2. The culture was carried out by shaking culture at 80 ° C. for 1 hour at 36 ° C., and after culturing, the cells were sown on a plate and observed. There was an increase. On the other hand, when a medium in which the same concentration of sucrose was added to the medium instead of molasses was used, propagation of general bacteria that did not decompose the oil was observed. It did not grow as much as it did. In addition, when a general bacterial medium (standard medium) was used, the number of bacteria, the number of colonies, and the type of bacteria were small, and the development of colonies was extremely poor.
【0038】培養菌添加の効果 総容量20Lの容器(うち、処理量8〜10L)を用い
て、菌液を20ml(0.1%の割合)添加し、通常の
馴養方法を行った。この結果、馴養開始7日以内で静置
時に水面に浮いた状態となり、種汚泥が死滅した。基質
である排水注入直後から、添加後6日までのORPの変
化を表5に示す。同時に、このときの基質注入直後から
24時間までのpHの継時変化、CODの変化を表6及
び表7にそれぞれ示す。菌液を添加しなかったものにつ
いても同様に測定した。表5、6、7において、基質
は、含油排水、具体的には処理設備の加圧浮上槽の水又
はそれを希釈したものであり、基質の数値は、基質自身
のORP、pH、CODであり、時間0の値は基質に活
性液を投入した直後のpH、CODである。Effect of the Addition of Culture Bacteria Using a container having a total volume of 20 L (including a treatment amount of 8 to 10 L), 20 ml (0.1% ratio) of the bacterial solution was added, and a normal acclimatization method was performed. As a result, the sludge floated on the surface of the water within 7 days after the start of acclimation, and the seed sludge was killed. Table 5 shows changes in ORP from immediately after injecting the wastewater as a substrate to 6 days after the addition. At the same time, the change in pH over time and the change in COD from immediately after the injection of the substrate to 24 hours are shown in Tables 6 and 7, respectively. The measurement was similarly performed for the sample to which no bacterial solution was added. In Tables 5, 6, and 7, the substrate is oil-containing wastewater, specifically, water in a pressurized flotation tank of a treatment facility or a dilution thereof, and the numerical value of the substrate is ORP, pH, and COD of the substrate itself. Yes, the value at time 0 is the pH and COD immediately after the addition of the active solution to the substrate.
【0039】[0039]
【表5】 [Table 5]
【0040】[0040]
【表6】 [Table 6]
【0041】[0041]
【表7】 [Table 7]
【0042】表から、菌を添加した場合、pHの減少、
CODの低下ともに無添加の場合と比較して早まった。
すなわち、菌を添加することにより、油の分解が促進さ
れていることが示された。From the table, it can be seen that when bacteria were added, the pH decreased,
Both of the COD reductions were accelerated as compared with the case where no additive was added.
That is, it was shown that the decomposition of oil was promoted by adding bacteria.
【0043】亜嫌気条件の効果 本発明に従って、DOを0.5〜0.3mg/Lの範囲
で亜嫌気状態で処理した後、好気条件にして曝気処理を
行った後、静置したものについて、CODの変化、ヘキ
サン抽出物(n−He抽出物)の変化、SSの変化を測
定した。結果を図2の(a)、(b)、(c)にそれぞ
れ示す。最初の亜嫌気状態をDOを1.5〜0.3mg
/L(平均1.5mg/L)の範囲で好気条件としたも
のについてのの測定結果についても図2に示す。CO
D、ヘキサン抽出物、SSの分析は、JIS K 01
02により行った。Effect of Sub-Anaerobic Condition According to the present invention, DO is treated in a sub-anaerobic state in the range of 0.5 to 0.3 mg / L, aerobically treated under aerobic conditions, and left standing. , The change in COD, the change in hexane extract (n-He extract), and the change in SS were measured. The results are shown in FIGS. 2 (a), (b) and (c), respectively. 1.5-0.3mg DO for first subanaerobic condition
FIG. 2 also shows the measurement results for aerobic conditions in the range of / L (average 1.5 mg / L). CO
The analysis of D, hexane extract and SS was conducted according to JIS K01.
02.
【0044】図2から、亜嫌気状態を経た処理は、好気
状態のみで行った処理に比べ、COD、ヘキサン抽出
物、SSについてすべて減少が早く、含油排水の分解処
理においてより好適であることが示された。From FIG. 2, it can be seen that the treatment under the sub-anaerobic condition reduces COD, hexane extract and SS all faster than the treatment performed only under the aerobic condition, and is more suitable for the decomposition treatment of oil-containing wastewater. It has been shown.
【0045】[0045]
【発明の効果】本発明によれば、切削油排水中の混合微
生物集団を集積培養し、排水流入時に0.01〜1%の
割合で処理排水に混合微生物集団に添加することによ
り、油分による種汚泥のショック死を防止し、馴養を可
能とするとともに、菌による活性汚泥法による処理が可
能となる。亜嫌気状態、好気状態、嫌気状態の各処理工
程を順に繰り返す回分式活性汚泥法で処理することによ
り、活性汚泥法では処理が困難な水溶性の切削油の含油
排水を処理することができる。なお、亜嫌気状態として
撹拌処理を行うことによって、切削油中の界面活性剤に
よる発泡を防止し、SS、ヘキサン抽出物の処理を高め
られる。According to the present invention, the mixed microbial population in the cutting oil wastewater is accumulated and cultured and added to the treated wastewater at a rate of 0.01 to 1% to the mixed microbial population at the rate of 0.01 to 1% when the wastewater flows into the wastewater. In addition to preventing shock death of seed sludge, acclimatization is enabled, and treatment by activated sludge method using bacteria becomes possible. By treating in a batch type activated sludge method in which the sub-anaerobic state, aerobic state, and anaerobic state processing steps are sequentially repeated, it is possible to treat oil-containing wastewater of a water-soluble cutting oil, which is difficult to treat in the activated sludge method. . By performing the stirring process in a sub-anaerobic state, foaming due to the surfactant in the cutting oil can be prevented, and the processing of the SS and hexane extracts can be enhanced.
【図1】図1は、本発明による回分式活性汚泥処理方法
を示す図である。FIG. 1 is a diagram showing a batch activated sludge treatment method according to the present invention.
【図2】図2は、亜嫌気条件の有無によるCOD、ヘキ
サン抽出物、SSの減少の差を示すグラフである。FIG. 2 is a graph showing the difference in reduction of COD, hexane extract, and SS depending on the presence or absence of sub-anaerobic conditions.
Claims (4)
養し、培養された混合微生物集団を排水流入時に添加す
ることを特徴とする回分式活性汚泥法による含油排水の
活性汚泥による処理方法。1. A method of treating oil-containing wastewater with activated sludge by a batch-type activated sludge method, wherein a mixed microorganism group in cutting oil wastewater is accumulated and cultured, and the cultured mixed microorganism group is added when the wastewater flows into the wastewater.
処理サイクルを順に繰り返すことを特徴とする請求項1
に記載の処理方法。2. The processing cycle of setting a sub-anaerobic state, an aerobic state, and an anaerobic state in order is repeated.
The processing method described in 1.
mg/L以下であるが、0mg/Lではない条件であっ
て、この亜嫌気状態の間に撹拌することを特徴とする請
求項2に記載の処理方法。3. The method according to claim 2, wherein the dissolved oxygen is about 0.5
The processing method according to claim 2, wherein the stirring is carried out during the sub-anaerobic state under a condition of not more than 0 mg / L but not more than 0 mg / L.
て、処理すべき含油排水と、窒素源としてカゼイン製ペ
プトン及び大豆ペプトンと、炭素原として糖蜜とを含む
ことを特徴とする培地。4. A growth medium for an oil-containing wastewater treatment fungus, which medium comprises oil-containing wastewater to be treated, casein peptone and soybean peptone as a nitrogen source, and molasses as a carbon source.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7905499A JP2000271589A (en) | 1999-03-24 | 1999-03-24 | Method for treating oil-containing drainage by activated sludge and culture medium for propagating bacteria for treating oil-containing drainage |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7905499A JP2000271589A (en) | 1999-03-24 | 1999-03-24 | Method for treating oil-containing drainage by activated sludge and culture medium for propagating bacteria for treating oil-containing drainage |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000271589A true JP2000271589A (en) | 2000-10-03 |
Family
ID=13679193
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7905499A Pending JP2000271589A (en) | 1999-03-24 | 1999-03-24 | Method for treating oil-containing drainage by activated sludge and culture medium for propagating bacteria for treating oil-containing drainage |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2000271589A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100942054B1 (en) | 2008-08-26 | 2010-02-11 | 주식회사 경우크린텍 | Advanced Wastewater Treatment Method and Treatment System by Batch Bioreactor |
KR100942053B1 (en) * | 2005-12-30 | 2010-02-24 | 에스케이케미칼주식회사 | Advanced Wastewater Treatment Method and Treatment System by Batch Bioreactor |
JP2016047490A (en) * | 2014-08-27 | 2016-04-07 | 水ing株式会社 | Method and apparatus for treating oil-containing wastewater |
CN106242082A (en) * | 2016-10-13 | 2016-12-21 | 中国神华能源股份有限公司 | A kind of biological inoculum screening and cultivation solidification equipment, method and application |
CN113443799A (en) * | 2021-06-25 | 2021-09-28 | 中国地质大学(北京) | Catalytic treatment process and system for converting hazardous waste oil-containing silt into solid waste |
CN113754181A (en) * | 2021-08-03 | 2021-12-07 | 杭州电子科技大学 | A kind of treatment method and device of polyester wastewater |
CN114835266A (en) * | 2022-05-13 | 2022-08-02 | 黄山聚电环保科技有限公司 | Method and device for treating high-concentration TGIC wastewater |
-
1999
- 1999-03-24 JP JP7905499A patent/JP2000271589A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100942053B1 (en) * | 2005-12-30 | 2010-02-24 | 에스케이케미칼주식회사 | Advanced Wastewater Treatment Method and Treatment System by Batch Bioreactor |
KR100942054B1 (en) | 2008-08-26 | 2010-02-11 | 주식회사 경우크린텍 | Advanced Wastewater Treatment Method and Treatment System by Batch Bioreactor |
JP2016047490A (en) * | 2014-08-27 | 2016-04-07 | 水ing株式会社 | Method and apparatus for treating oil-containing wastewater |
CN106242082A (en) * | 2016-10-13 | 2016-12-21 | 中国神华能源股份有限公司 | A kind of biological inoculum screening and cultivation solidification equipment, method and application |
CN106242082B (en) * | 2016-10-13 | 2023-04-28 | 中国神华能源股份有限公司 | Biological strain screening, culturing and solidifying device, method and application |
CN113443799A (en) * | 2021-06-25 | 2021-09-28 | 中国地质大学(北京) | Catalytic treatment process and system for converting hazardous waste oil-containing silt into solid waste |
CN113754181A (en) * | 2021-08-03 | 2021-12-07 | 杭州电子科技大学 | A kind of treatment method and device of polyester wastewater |
CN113754181B (en) * | 2021-08-03 | 2023-12-08 | 杭州电子科技大学 | Polyester wastewater treatment method and device |
CN114835266A (en) * | 2022-05-13 | 2022-08-02 | 黄山聚电环保科技有限公司 | Method and device for treating high-concentration TGIC wastewater |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105645710B (en) | A kind of method that mud decrement is carried out using complex microorganism preparations | |
CN102268394A (en) | Method of amplification culture of microorganism for waste water treatment and method of microorganism waste water treatment | |
EP1042236B1 (en) | A method of preparing a microbial culture for wastewater treatment | |
CN109052822A (en) | A kind of microbial inoculum treatment process of town sewage | |
CN108773912B (en) | Microbial inoculum treatment process for livestock and poultry breeding sewage | |
JP2000271589A (en) | Method for treating oil-containing drainage by activated sludge and culture medium for propagating bacteria for treating oil-containing drainage | |
CN114394673B (en) | Biological fermentation pretreatment method for high-concentration organic wastewater and application thereof | |
Das et al. | Two stage treatability and biokinetic study of dairy wastewater using bacterial consortium and microalgae | |
Kosseva et al. | Thermophilic bioremediation of whey: effect of physico-chemical parameters on the efficiency of the process | |
JP2006042774A (en) | New Yarrowia yeast and biological treatment method of wastewater | |
CN114620900B (en) | Denitrification treatment method for kitchen anaerobic wastewater | |
CN109250825A (en) | A kind of bio-synergistic sewage-treating agent and preparation method thereof | |
KR20030071604A (en) | Process of the treatment of high-concentrated and non-biodegradable industrial wastewater using modified-cultured facultative bacteria | |
JPH08192180A (en) | Activated sludge treatment method for organic wastewater | |
KR19990084124A (en) | Bacteria group of bacillus spp in the aerobic reacting device and method for treating nihgtsoil, stackbreeding waste water, leachate and industrial organic wastewater | |
CN113023901A (en) | Construction method of salt-tolerant microbial group and application of salt-tolerant microbial group in field of high-salinity wastewater treatment | |
CN110551665A (en) | method for culturing tobacco sewage flora | |
KR200172809Y1 (en) | Bacteria group of bacillus spp in the aerobic reacting device for treating nihgtsoil, stackbreeding waste water, leachate and industrial organic wastewater | |
CN117511828B (en) | High-concentration domestic sewage treatment microbial inoculum after septic tank and preparation method thereof | |
JPH06106198A (en) | Method and device for microbiological reduction of amount of surplus sludge | |
CN112725242B (en) | Special microbial inoculum for strengthening sewage centralized treatment of activated sludge and preparation method thereof | |
Dragičević et al. | The potential of dairy wastewater for denitrification. | |
Jung et al. | Nitrogenous compounds transformation by the sludge solubilization under alternating aerobic and anaerobic conditions | |
KR100391136B1 (en) | Bacteria group of bacillus spp in treating equipment and method for sewage and waste water | |
KR960009381B1 (en) | Activated sludge spawn agent for water treatment and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20050609 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20050708 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20051129 |