JPH0125636B2 - - Google Patents
Info
- Publication number
- JPH0125636B2 JPH0125636B2 JP10997680A JP10997680A JPH0125636B2 JP H0125636 B2 JPH0125636 B2 JP H0125636B2 JP 10997680 A JP10997680 A JP 10997680A JP 10997680 A JP10997680 A JP 10997680A JP H0125636 B2 JPH0125636 B2 JP H0125636B2
- Authority
- JP
- Japan
- Prior art keywords
- high concentration
- tank
- carbon source
- organic carbon
- reaction tank
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000006243 chemical reaction Methods 0.000 claims description 23
- 239000007788 liquid Substances 0.000 claims description 23
- 239000010802 sludge Substances 0.000 claims description 23
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 238000005273 aeration Methods 0.000 claims description 15
- 239000012895 dilution Substances 0.000 claims description 15
- 238000010790 dilution Methods 0.000 claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 239000002699 waste material Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 238000000926 separation method Methods 0.000 claims description 6
- 238000001556 precipitation Methods 0.000 claims description 2
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 11
- 239000011550 stock solution Substances 0.000 description 10
- JVMRPSJZNHXORP-UHFFFAOYSA-N ON=O.ON=O.ON=O.N Chemical compound ON=O.ON=O.ON=O.N JVMRPSJZNHXORP-UHFFFAOYSA-N 0.000 description 6
- 239000010800 human waste Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000002351 wastewater Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000001477 organic nitrogen group Chemical group 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 2
- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
Description
本発明は、し尿などの高濃度廃液を処理する方
法に関し、特に無希釈、無薬注でし尿その他の廃
液を短日で良好な水質にまで処理することのでき
る方法に関する。
通常の活性汚泥法の適用範囲を超えた高濃度廃
水(BOD、総窒素(以下、T―Nと云う。)の濃
度の高い廃水、例えばし尿、浄化槽汚泥、家畜糞
尿など)を無希釈、短時日で処理する場合、高濃
度活性汚泥(MLSS10000ppm以上)を、通常の
散気管(多孔性デイフユーザー、デイスクフユー
ザーなど)よりも酸素供給能力の大きい曝気装置
を適用した反応槽に導いて処理する場合、同反応
槽では、流入有機態窒素、アンモニア窒素の酸化
(硝化)と同時にその酸化生成物である亜硝酸、
硝酸性窒素のN2への還元(脱窒)が起きる。し
かし、このときのT―N除去率は原液中の有機物
量(有機炭素源として利用可能な)によつて不可
抗力的な限界がある。
すなわち脱窒反応が起きるには有機炭素源が必
要であるが有機炭素源が少ないと脱窒率は制限さ
れる。そしてこの場合原液BODを有機炭素源と
していることからこの流入量が少ないと脱窒率は
抑制されるのである。
また、これら原液の無希釈処理では、一般には
アンモニア性窒素は亜硝酸性窒素にまでしか酸化
されないが、この亜硝酸性窒素は浄化微生物に対
して毒性があり、このためアンモニア性窒素を亜
硝酸性窒素に酸化する亜硝酸菌の酸化能力が劣下
して完全なるアンモニア性窒素の除去には到ら
ず、容易に放流可能な水質レベルに到達しない。
このように、前記する無希釈反応工程(硝化工
程)では次の2つの問題点があつた。
(1) 原液中BOD/T―NによつてT―N除去率
に不可抗力的な限界がある。
すなわち、BOD/T―Nは有機炭素源と脱
窒素すべき窒素量との比率であり、この値が小
さいと脱窒率は抑制される。
(2) 亜硝酸性窒素が蓄積して生物毒性が発現し完
全なるアンモニア性窒素の除去が達成できな
い。
本発明は、上記の問題点を解決する目的でなさ
れたものであつて、高濃度廃液を無希釈又は低希
釈倍率で活性汚泥処理する方法において、上記高
濃度廃液を酸素供給能力の大きい曝気装置を設け
かつ槽内の活性汚泥を高濃度に維持した単一の反
応槽に導き、上記反応槽に有機炭素源を注入して
上記高濃度廃液を硝化脱窒処理し、その後処理液
を沈殿槽に導いて固液分離を行うことを要旨とす
るものである。
以下、添付図面等を用いて本発明を詳細に説明
する。
第1図は、本発明によるプロセスの基本構成を
示す概要図である。
第1図において、図示省略のデカンタまたはド
ラムスクリーンなどの除渣機で除渣した原液11
(高濃度廃液)は、ライン1から無希釈のまま本
プロセスに流入し、原液11は通常の散気管(多
孔性デイフユーザー、デイスクフユーザーなど)
よりも酸素供給能力の大きい曝気装置7を付帯し
て、空気8を供給し、さらに高濃度活性汚泥を適
用した無希釈反応工程を行なう反応槽2へ流入す
る。ここで使用する曝気装置7は、ブロワーから
供給された圧縮空気を分散微細化させるもので、
円筒状(但し、上部はメクラとなつており、ちよ
うどコツプを逆さまにしたもの)の高速度回転体
である。内部は中空となつているが、供給空気は
本回転体内に供給され、オーバーフローして外部
側壁において液との摩擦により微細気泡となる。
したがつて、実際の使用時に、酸素供給速度を調
整するにはこの回転体の回転数と供給空気量を変
化させればよい。酸素供給速度を増加するには、
回転数及び空気量を増加させ、逆に酸素供給速度
を減少させるには回転数及び空気量を減少させ
る。この反応槽2では原液11中のBODの除去
と有機態窒素、アンモニア性窒素を酸化し、さら
にN2まで還元することを同時に行う。その反応
状況は次の通りである。
(第1式〜第4式)
硝化処理(NH4―N→NO2―N→NO3―N)
NH4 ++1.5O2→NO2 -+H2O+2H-
……第1式
NO2 -+0.5O2→NO3 - ……第2式
脱窒処理
2NO3 -+10H→N2↑+4H2O+20H-
……第3式
2NO2 -+6H→N2↑+2H2O+20H-
……第4式
この処理反応工程に外部より、有機態窒素、ア
ンモニア性窒素の酸化で生じた亜硝酸、硝酸性窒
素の還元に必要な有機炭素源12をライン9(例
えばメタノール、酢酸など)から注入する。
なお、酸素供給能力の大きい曝気装置7を付帯
するのは次の理由による。すなわち単位反応槽容
量当りのO2消費速度が大となり濃度レベルが高
いので反応速度大となるためである。注入された
空気8および有機炭素源12によつて、原液11
は反応槽2で効率良く硝化脱窒処理されたのち、
反応槽排出液13はライン14を通り後段の分離
槽3に導かれ、同分離槽3で固液分離、汚泥濃縮
が行なわれ、同分離槽3での液分は処理水15と
してライン4から抜き出され、同処理水15の一
部はライン10からライン1へ循環返送され、残
りの処理水15は系外へ放出される。一方、分離
槽3での汚泥の一部は連続的にライン6から前記
のライン1へ返送汚泥16として返送循環すると
共に余剰汚泥17をライン5から引抜く。この余
剰汚泥17は図示省略の汚泥処理施設へ送られ
る。
実験例
次に第1図に図示するプロセスについて連続試
験を行なつた結果を示す。
試験条件は次の通りである。
(1) 原液11
除渣後生し尿、某処理場より調達した破砕生
し尿のデカンター分離液
(2) 処理日数(反応槽容量/原液(無希釈し尿)
流量)……2日
(3) 槽内汚泥濃度……(10000〜13000(ppm)
(4) 希釈倍率……無希釈
(5) 汚泥返送率(返送汚泥量/原液流量)×100%
……200〜300%
(6) 反応槽2内の溶存酸素(DO)濃度……3〜
4.5(ppm)
(7) 曝気設備 高性能曝気装置(第1図に示す曝
気装置)
(8) 有機・炭素量……N/Kgに対してCH3OH
2Kg
実験の結果を第1表に示す。
The present invention relates to a method for treating highly concentrated waste liquids such as human waste, and particularly to a method that can treat human waste and other waste liquids to good water quality in a short period of time without dilution or chemical injection. High-concentration wastewater (BOD, wastewater with a high concentration of total nitrogen (hereinafter referred to as TN), such as human waste, septic tank sludge, livestock manure, etc.) that exceeds the scope of application of the normal activated sludge method can be processed without dilution in a short time. In the case of treatment, high-concentration activated sludge (MLSS 10,000 ppm or more) is guided into a reaction tank equipped with an aeration device that has a larger oxygen supply capacity than a normal aeration pipe (porous diffuser, disk user, etc.). In the same reaction tank, the inflow organic nitrogen and ammonia nitrogen are oxidized (nitrified) and its oxidation product nitrite,
Reduction of nitrate nitrogen to N2 (denitrification) occurs. However, the TN removal rate at this time has an irresistible limit depending on the amount of organic matter in the stock solution (which can be used as an organic carbon source). That is, an organic carbon source is necessary for the denitrification reaction to occur, but if the organic carbon source is small, the denitrification rate is limited. In this case, since the undiluted BOD is used as the organic carbon source, if the inflow amount is small, the denitrification rate will be suppressed. In addition, in the undiluted treatment of these stock solutions, ammonia nitrogen is generally oxidized only to nitrite nitrogen, but this nitrite nitrogen is toxic to purification microorganisms, so ammonia nitrogen is oxidized to nitrite nitrogen. The oxidizing ability of nitrite bacteria, which oxidizes to ammonia nitrogen, deteriorates, and complete removal of ammonia nitrogen is not achieved, and the water quality does not reach a level that can be easily discharged. As described above, the above-mentioned non-dilution reaction step (nitrification step) had the following two problems. (1) There is an unavoidable limit to the TN removal rate depending on the BOD/TN in the stock solution. That is, BOD/TN is the ratio between the organic carbon source and the amount of nitrogen to be denitrified, and when this value is small, the denitrification rate is suppressed. (2) Nitrite nitrogen accumulates and becomes biologically toxic, making complete removal of ammonia nitrogen impossible. The present invention has been made for the purpose of solving the above-mentioned problems, and provides a method for treating high-concentration waste liquid with activated sludge without dilution or at a low dilution rate, using an aeration device with a large oxygen supply capacity. The activated sludge in the tank is guided to a single reaction tank in which the activated sludge is maintained at a high concentration, and an organic carbon source is injected into the reaction tank to perform nitrification and denitrification treatment on the high concentration waste liquid, and then the treated liquid is transferred to a sedimentation tank. The gist of this is to conduct solid-liquid separation by introducing Hereinafter, the present invention will be explained in detail using the accompanying drawings and the like. FIG. 1 is a schematic diagram showing the basic configuration of the process according to the present invention. In FIG. 1, the stock solution 11 is removed from the residue using a decanter or drum screen (not shown).
(highly concentrated waste liquid) flows into this process without dilution from line 1, and the raw liquid 11 is passed through a normal aeration pipe (porous diffuser, disk user, etc.).
An aeration device 7 having a larger oxygen supply capacity than the sludge is attached to supply air 8, and the sludge flows into a reaction tank 2 in which a non-dilution reaction process using highly concentrated activated sludge is performed. The aeration device 7 used here disperses and atomizes the compressed air supplied from the blower.
It is a high-speed rotating body with a cylindrical shape (however, the top is blank, which is similar to an upside-down tip). Although the interior is hollow, the supplied air is supplied into the rotating body, overflows, and forms fine bubbles on the external side wall due to friction with the liquid.
Therefore, in actual use, the oxygen supply rate can be adjusted by changing the rotational speed of this rotating body and the amount of supplied air. To increase the oxygen delivery rate,
To increase the number of revolutions and the amount of air, and conversely to decrease the oxygen supply rate, reduce the number of revolutions and the amount of air. In this reaction tank 2, the removal of BOD in the stock solution 11, the oxidation of organic nitrogen and ammonia nitrogen, and further reduction to N2 are performed simultaneously. The reaction situation is as follows. (Equations 1 to 4) Nitrification treatment (NH 4 -N→NO 2 -N→NO 3 -N) NH 4 + +1.5O 2 →NO 2 - +H 2 O+2H -
...1st formula NO 2 - +0.5O 2 →NO 3 - ...2nd formula Denitrification treatment 2NO 3 - +10H→N 2 ↑+4H 2 O+20H -
...3rd formula 2NO 2 - +6H→N 2 ↑+2H 2 O+20H -
...Equation 4 In this treatment reaction step, an organic carbon source 12 necessary for reducing nitrous acid and nitrate nitrogen generated by oxidation of organic nitrogen and ammonia nitrogen is externally supplied to line 9 (for example, methanol, acetic acid, etc.). Inject from. The reason why the aeration device 7 with a large oxygen supply capacity is provided is as follows. In other words, this is because the O 2 consumption rate per unit reaction tank capacity is high and the concentration level is high, resulting in a high reaction rate. By injected air 8 and organic carbon source 12, stock solution 11
After being efficiently nitrified and denitrified in reaction tank 2,
The reaction tank discharge liquid 13 is led to the downstream separation tank 3 through a line 14, where solid-liquid separation and sludge concentration are performed. A part of the treated water 15 is recycled from line 10 to line 1, and the remaining treated water 15 is discharged outside the system. On the other hand, a part of the sludge in the separation tank 3 is continuously circulated from line 6 to line 1 as return sludge 16, and excess sludge 17 is pulled out from line 5. This surplus sludge 17 is sent to a sludge treatment facility (not shown). EXPERIMENTAL EXAMPLE Next, the results of continuous tests on the process shown in FIG. 1 will be shown. The test conditions are as follows. (1) Raw solution 11 Human waste after sediment removal, decanter separated liquid of crushed raw human waste procured from a certain treatment plant (2) Number of processing days (reaction tank capacity / raw solution (undiluted human waste)
Flow rate)...2 days (3) Sludge concentration in tank...(10000 to 13000 (ppm)) (4) Dilution ratio...No dilution (5) Sludge return rate (return sludge amount/undiluted solution flow rate) x 100%
...200~300% (6) Dissolved oxygen (DO) concentration in reaction tank 2...3~
4.5 (ppm) (7) Aeration equipment High-performance aeration equipment (aeration equipment shown in Figure 1) (8) Organic carbon content... CH 3 OH for N/Kg
The results of the 2Kg experiment are shown in Table 1.
【表】
本発明はこのように、高濃度廃液を無希釈又は
低希釈倍率で活性汚泥処理する方法において、上
記高濃度廃液を酸素供給能力の大きい曝気装置を
設けかつ槽内の活性汚泥を高濃度に維持した単一
の反応槽に導き、上記反応槽に有機炭素源を注入
して上記高濃度廃液を硝化脱窒処理し、その後処
理液を沈殿槽に導いて固液分離を行うので、次の
ような効果が得られる。
有機炭素源を注入しない場合は、この工程の
T―N除去率Aは、原液BOD/T―Nによつ
て第5式のような不可抗力的な限界がある。す
なわち、原液BODを有機炭素源としているの
みであるので、原液BODの流入量が少なくな
るとT―N除去率Aが抑制され限界が生じるこ
とになる。
A=L0/a×N0 …(第5式)
ただし、
L0:原液中BOD濃度(Kg/m3)
N0:原液中T―N濃度(Kg/m3)
a:NO2―N又はNO3―N1Kg環元するに
必要なBOD量(Kg)
しかし、本発明のようにあらためて外部より
有機炭素源を注入すれば有機炭素源が増えるか
ら、T―N除去率Aの上限値がさらに高まるこ
とになる。
高濃度廃水の無希釈反応工程では、流入アン
モニア性窒素は亜硝酸性窒素にまでしか酸化さ
れず、この亜硝酸性窒素は生物毒性がありした
がつてアンモニア性窒素の除去能力が制限され
る。外部から有機炭素源を注入すれば亜硝酸性
窒素の濃度レベルが下がりアンモニア性窒素の
除去能力が向上し、高効率のT―N除去率が達
成できる。
なお、本発明は次の条件で行なえばさらに上記
の効率が高まることになる。
(1) 汚泥濃度を可能な限り高めること。
(2) 一般の散気管より酸素供給能力の大きい曝気
装置を適用すること。
(3) 対象高濃度廃水を3倍以下の希釈倍率で処理
すること。[Table] In this way, the present invention provides a method for treating high concentration waste liquid with activated sludge without dilution or at a low dilution rate, by providing an aeration device with a large oxygen supply capacity for the high concentration waste liquid and increasing the activated sludge in the tank. The high concentration waste liquid is led to a single reaction tank where the concentration is maintained, an organic carbon source is injected into the reaction tank, the high concentration waste liquid is subjected to nitrification and denitrification treatment, and the treated liquid is then led to a precipitation tank to perform solid-liquid separation. The following effects can be obtained. When an organic carbon source is not injected, the TN removal rate A in this step has an irresistible limit as shown in equation 5 depending on the stock solution BOD/TN. That is, since the undiluted solution BOD is only used as an organic carbon source, when the inflow amount of the undiluted solution BOD decreases, the TN removal rate A is suppressed and a limit occurs. A=L 0 /a×N 0 (5th formula) where, L 0 : BOD concentration in stock solution (Kg/m 3 ) N 0 : TN concentration in stock solution (Kg/m 3 ) a: NO 2 - N or NO 3 - Amount of BOD required for N1Kg ring formation (Kg) However, if an organic carbon source is injected from outside as in the present invention, the organic carbon source increases, so the upper limit of the TN removal rate A is will further increase. In the no-dilution reaction process of highly concentrated wastewater, the influent ammonia nitrogen is oxidized only to nitrite nitrogen, which is biotoxic and thus limits the ability to remove ammonia nitrogen. By injecting an organic carbon source from the outside, the concentration level of nitrite nitrogen is reduced, the ammonia nitrogen removal ability is improved, and a highly efficient TN removal rate can be achieved. Note that the efficiency described above can be further improved if the present invention is carried out under the following conditions. (1) Increase sludge concentration as much as possible. (2) Apply an aeration device with a larger oxygen supply capacity than a general aeration pipe. (3) Target high concentration wastewater shall be treated at a dilution rate of 3 times or less.
第1図は本発明の基本プロセスフローを示す概
要図である。
2…反応槽、7…酸素供給能力の大きい曝気装
置、8…空気、9…有機炭素源、11…原液。
FIG. 1 is a schematic diagram showing the basic process flow of the present invention. 2... Reaction tank, 7... Aeration device with large oxygen supply capacity, 8... Air, 9... Organic carbon source, 11... Stock solution.
Claims (1)
泥処理する方法において、上記高濃度廃液を酸素
供給能力の大きい曝気装置を設けかつ槽内の活性
汚泥を高濃度に維持した単一の反応槽に導き、上
記反応槽に有機炭素源を注入して上記高濃度廃液
を硝化脱窒処理し、その後処理液を沈殿槽に導い
て固液分離を行うことを特徴とする高濃度廃液の
処理方法。1. In a method of treating high concentration waste liquid with activated sludge without dilution or at a low dilution ratio, a single reaction tank is provided with an aeration device having a large oxygen supply capacity and the activated sludge in the tank is maintained at a high concentration. A method for treating a high concentration waste liquid, comprising: injecting an organic carbon source into the reaction tank to subject the high concentration waste liquid to nitrification and denitrification treatment, and then introducing the treated liquid to a precipitation tank to perform solid-liquid separation. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10997680A JPS5735998A (en) | 1980-08-11 | 1980-08-11 | Disposal of highly concentrated waste liquid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10997680A JPS5735998A (en) | 1980-08-11 | 1980-08-11 | Disposal of highly concentrated waste liquid |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5735998A JPS5735998A (en) | 1982-02-26 |
JPH0125636B2 true JPH0125636B2 (en) | 1989-05-18 |
Family
ID=14523916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10997680A Granted JPS5735998A (en) | 1980-08-11 | 1980-08-11 | Disposal of highly concentrated waste liquid |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5735998A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60166096A (en) * | 1984-02-03 | 1985-08-29 | Shoshi Hiraoka | Treatment of waste water |
CN102795703B (en) * | 2012-02-17 | 2013-12-18 | 华东理工大学 | Deep treatment method of nitrate-containing water |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5814838B2 (en) * | 1978-12-20 | 1983-03-22 | 株式会社クボタ | Human waste disposal method |
JPS5592197A (en) * | 1978-12-28 | 1980-07-12 | Kubota Ltd | Processing method of water |
JPS5724699A (en) * | 1980-07-17 | 1982-02-09 | Mitsubishi Heavy Ind Ltd | Disposal of highly concentrated waste liquid |
-
1980
- 1980-08-11 JP JP10997680A patent/JPS5735998A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5735998A (en) | 1982-02-26 |
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