JPH0218915B2 - - Google Patents
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- Publication number
- JPH0218915B2 JPH0218915B2 JP12344186A JP12344186A JPH0218915B2 JP H0218915 B2 JPH0218915 B2 JP H0218915B2 JP 12344186 A JP12344186 A JP 12344186A JP 12344186 A JP12344186 A JP 12344186A JP H0218915 B2 JPH0218915 B2 JP H0218915B2
- Authority
- JP
- Japan
- Prior art keywords
- gas
- carbon dioxide
- human waste
- acid
- 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 - Lifetime
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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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Landscapes
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Treatment Of Sludge (AREA)
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、上向流式嫌気性汚泥床法によりし尿
系汚水を処理する方法及び装置に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method and apparatus for treating human waste wastewater by an upflow anaerobic sludge bed method.
上向流式嫌気性汚泥床法(以下、UASB法と
略記する)は、廃水をメタン発酵するための方法
として近年開発された方法であつて、原廃水を発
酵槽の下部より上向流として流入させ、菌の付着
担体を用いることなく、汚泥(菌)をフロツク化
若しくは粒状化せしめることにより汚泥床(スラ
ツジベツド)を形成させ、発酵槽中に高濃度の微
生物を確保するためにより高容積負荷を許容しう
る嫌気的微生物処理技術であつて、その装置とし
ては低負荷時の被処理液の短絡を防止するために
底部に被処理液を均一に流入させるための分配流
入管を備え、かつ、上部にガス−固−液の三相分
離装置を備えたものである(下水道協会誌
Vol.22、No.255、1985/8、67〜77頁)。
The upflow anaerobic sludge bed method (hereinafter abbreviated as UASB method) is a method developed in recent years as a method for methane fermentation of wastewater. A sludge bed is formed by flocculating or granulating the sludge (bacteria) without using a carrier for bacteria to adhere to, and a higher volume load is applied to ensure a high concentration of microorganisms in the fermenter. This is an anaerobic microbial treatment technology that allows for the treatment of liquids, and the equipment is equipped with a distribution inlet pipe to uniformly flow the liquid to be treated at the bottom in order to prevent short circuits of the liquid to be treated at low loads, and , equipped with a gas-solid-liquid three-phase separation device at the top (Journal of the Japan Sewage Works Association)
Vol. 22, No. 255, 1985/8, pp. 67-77).
このUASB法は、廃液の質的差異により採用
できる場合と採用できない場合のあることが知ら
れており、この方法をし尿系廃水のメタン発酵に
利用できるかどうかを検討した報告例はこれまで
のところ皆無である。 It is known that this UASB method may or may not be adopted depending on the quality of the waste liquid, and there have been no reports to date on whether this method can be used for methane fermentation of night soil wastewater. There are none at all.
本発明は、し尿系汚水をUASB法により処理
する方法を提供することを目的とする。
An object of the present invention is to provide a method for treating human waste water using the UASB method.
本発明は、し尿系汚水を、予め酸発酵槽におい
て酸発酵させると共に含有するSSをスカムとし
て除去した後、底部に分配流入管を、上部に気−
固−液分離部を有する汚泥床式メタン発酵反応槽
中に上向流で通水してメタン発酵処理を行なうに
際し、酸発酵槽からの流出液に炭酸ガスを吸収せ
しめた後メタン発酵反応槽に供給することを特徴
とするし尿系汚水の処理方法及び該方法を実施す
るための装置である。
In the present invention, human waste wastewater is subjected to acid fermentation in an acid fermentation tank, and the SS contained therein is removed as scum.
When performing methane fermentation treatment by passing water in an upward flow into a sludge bed type methane fermentation reaction tank having a solid-liquid separation section, carbon dioxide gas is absorbed into the effluent from the acid fermentation tank. A method for treating human waste wastewater, characterized in that the wastewater is supplied to a person, and an apparatus for carrying out the method.
従来のし尿系汚水のメタン発酵処理は、メタン
発酵槽内におけるできるだけ長いし尿滞留時間を
硬保するために、長時間滞留可能な完全混合式消
化槽、固定床式上向流嫌気性反応槽及び流動床式
嫌気性反応槽が用いられている。これらは何れも
メタン菌等の嫌気性菌のフロツク(径約0.5mm以
下)の形成が、これらの菌の担体に対する付着能
力を利用して構成された処理方法であつて、基質
としてのし尿はこれらの菌のフロツクの形成や担
体への付着に対し悪影響を与えることがないの
で、非効率ながらし尿系汚水を希釈することな
く、そのまま処理することが可能であつた。 Conventional methane fermentation treatment of human waste waste requires a fully mixed digester that can retain human waste for a long time, a fixed bed upward flow anaerobic reaction tank, and A fluidized bed anaerobic reactor is used. All of these treatment methods utilize the ability of these bacteria to adhere to carriers to form flocs (approximately 0.5 mm or less in diameter) of anaerobic bacteria such as methane bacteria, and human waste is used as a substrate. Since there is no adverse effect on the formation of flocs of these bacteria or their adhesion to carriers, it has been possible to treat human waste wastewater as it is without diluting it, although this is inefficient.
一方、UASB法は、メタン菌等の嫌気性菌の
発酵槽内における保持力ないしは保持量を大とす
るために、担体等の菌の付着媒体を用うることな
く、菌体自身を自己固定化せしめ、即ち菌体が
0.5mm〜5mm程度の顆粒状に凝集したグラニユー
ルを形成せしめ、該グラニユールにより汚泥床
(汚泥のブランケツト層)を形成させ、該汚泥床
中に上向流で廃水を通してメタン発酵を行う方法
であつて、特定の有機性廃水を高効率で処理でき
る方法である。 On the other hand, in the UASB method, in order to increase the retention power or amount of anaerobic bacteria such as methane bacteria in the fermenter, the bacteria self-immobilize without using a carrier or other adhesion medium for the bacteria. Seshime, that is, bacterial cells
A method in which granules aggregated into granules of about 0.5 mm to 5 mm are formed, a sludge bed (sludge blanket layer) is formed by the granules, and wastewater is passed through the sludge bed in an upward flow for methane fermentation. , is a method that can treat specific organic wastewater with high efficiency.
本発明者らは、特定の有機性廃水に対してでは
あるが、高効率でメタン発酵処理を行ないうる
UASB法にし尿を直接適用することを試みたが、
汚泥床を形成している菌体が顆粒状に凝集してい
るグラニユールがスカムと共に浮上し流失されて
しまい所期の目的を達成しえないことを見いだし
た。 The present inventors have demonstrated that methane fermentation can be carried out with high efficiency for specific organic wastewater.
I tried applying human urine directly to the UASB method, but
It was discovered that the granule, in which the bacterial cells that form the sludge bed aggregate into granules, floats up together with the scum and is washed away, making it impossible to achieve the intended purpose.
そこで、UASB反応槽を2基直列に連結して
使用し、前段のUASB反応槽において酸発酵と
し尿中のSSのスカム化による浮上分離を行なわ
せ、後段のUASB反応槽によつてSS濃度がほぼ
5000mg/以下に減少した酸発酵し尿を処理した
ところ、後段のUASB反応槽でグラニユールが
流出することなく、順調にメタン発酵することが
できたが、UASB反応槽より流出するメタン発
酵処理流出水中にはなお2500mg/以上の揮発性
有機酸が残存し、供試し尿として用いたBOD濃
度に対しBOD除去率は70%を越えることはなく、
平均除去率は68%であつた。この結果であつても
十分に満足できる処理成積ではあるものの、後段
のUASB法にかかる負荷を低減させ高度処理を
行ない処理コストを下げるためには、BOD除去
率を更に増加させることが有効であると考え、更
に前記の揮発性有機酸の残在率が高い理由につい
て検討を行なつた。 Therefore, two UASB reactors are connected in series, and the first stage UASB reactor performs acid fermentation and flotation separation by scum formation of SS in urine, and the second stage UASB reactor performs the SS concentration. almost
When the acid-fermented human waste reduced to less than 5,000mg was processed, methane fermentation was successfully carried out without any granules flowing out in the subsequent UASB reaction tank. However, more than 2500 mg/volatile organic acid remained, and the BOD removal rate did not exceed 70% compared to the BOD concentration used as the sample urine.
The average removal rate was 68%. Although this result is a sufficiently satisfactory processing result, it is effective to further increase the BOD removal rate in order to reduce the load on the subsequent UASB method, perform advanced processing, and lower processing costs. We thought that this was the case, and further investigated the reason for the high residual rate of volatile organic acids.
前記二段階処理法においては、前段の発酵槽は
必らずしもUASB反応槽を用いる必要はないが、
上向流反応槽とし酸発酵と共にスカムの発生を促
進する必要がある。従つて、流入SSの大径のフ
ロツクを形成させる必要上ガス撹拌や機械撹拌等
を行なうことなく、発生するガスによつてのみ穏
和に撹拌することによりフロツクの解体を防ぎつ
つスカムの発生を促がすため、発生ガスは短時間
に一過流的に該前段の反応槽中を上昇するに過ぎ
ず、十分な気液接触が行なわれないので、発生ガ
ス中の炭酸ガスが酸発酵液中に十分に吸収されな
いこととなる。その結果後段のUASB反応槽に
おいてはし尿中のアンモニアを中和するのに十分
な酸濃度が不足し、もし揮発性有機酸濃度0とな
つた場合の推定値は8.7とメタン発酵菌について
好ましいPH条件(6.9〜8.2)から大幅にはずれた
値となる。 In the two-stage treatment method, the first stage fermenter does not necessarily need to be a UASB reaction tank, but
It is necessary to use an upflow reaction tank to promote acid fermentation and scum generation. Therefore, since it is necessary to form a large-diameter floc of the inflowing SS, it is possible to prevent the disintegration of the floc and to promote the generation of scum by gently stirring only with the generated gas without using gas agitation or mechanical agitation. In order to remove the gas, the generated gas only rises in the first stage reaction tank in a short period of time, and sufficient gas-liquid contact does not occur, so that the carbon dioxide in the generated gas is absorbed into the acid fermentation liquid. It will not be absorbed sufficiently. As a result, the acid concentration in the subsequent UASB reaction tank is insufficient to neutralize the ammonia in the human waste, and if the volatile organic acid concentration becomes 0, the estimated value is 8.7, which is the preferred pH for methane-fermenting bacteria. The value is significantly different from the conditions (6.9 to 8.2).
事実、後段のUASB反応槽に極めて活性の高
いメタン発酵菌のグラニユールを充填してし尿の
処理実験を開始したところ、実験開始直後はメタ
ン発酵菌の作用が活発であるため揮発性有機酸が
多量に分解され、流出する処理水中の揮発性有機
酸濃度が低く、従つてBOD除去率も80%高かつ
た。しかしながら、時間の経過と共に処理水中の
揮発性有機酸濃度の増加が見られ、処理水中の揮
発性有機酸濃度約2700mg/で定常状態となつ
た。 In fact, when we started a human waste treatment experiment by filling the latter-stage UASB reaction tank with Granule, a highly active methane-fermenting bacterium, we found that immediately after the start of the experiment, the methane-fermenting bacterium was active, resulting in a large amount of volatile organic acids. The concentration of volatile organic acids in the effluent treated water was low, and the BOD removal rate was 80% higher. However, as time passed, the concentration of volatile organic acids in the treated water increased, and the concentration of volatile organic acids in the treated water reached a steady state of about 2,700 mg/.
この時のPHは、残在揮発性有機酸濃度とアンモ
ニアとの中和平衡によつて約8.2で安定していた
が、BOD除去率は67%と低い状態で推移した。 At this time, the pH remained stable at approximately 8.2 due to neutralization equilibrium between the residual volatile organic acid concentration and ammonia, but the BOD removal rate remained low at 67%.
その原因は、実験開始直後の菌の活性が高い段
階においてBOD除去率が高く、従つて処理水中
の揮発性有機酸濃度が低い段階において、処理水
のPH即ち反応槽内のPHがメタン発酵菌にとつて好
ましいPHよりも高くなり、従つてメタン発酵菌の
活性が低下し、この活性の低下に伴ない処理水中
の有機酸濃度が次第に高くなり、2700mg/で定
常状態に達したものと解される。 The reason for this is that the BOD removal rate is high at the stage immediately after the start of the experiment when the bacteria are highly active, and when the concentration of volatile organic acids in the treated water is low, the PH of the treated water, that is, the PH in the reaction tank, is lower than that of the methane-fermenting bacteria. Therefore, the activity of methane-fermenting bacteria decreased, and as this activity decreased, the organic acid concentration in the treated water gradually increased, reaching a steady state at 2700 mg/mL. be done.
事実、実験開始直後の処理水のPHは高く、最高
8.4に達した。 In fact, the pH of the treated water immediately after the start of the experiment was high, reaching the highest level.
Reached 8.4.
以上の結果から、第1段階においてし尿系廃水
の有機酸発酵とSSの除去を行なつた後第2段階
においてUASB処理を行なう二段式のUASB法
において、外部よりPH調節を行なわない場合に
は、後段のUASB反応において揮発性有機酸が
必らず残留することにより、メタン発酵の生じう
るPH8.2以下に発酵槽内の液が維持されることが
わかつた。 From the above results, in the two-stage UASB method, in which organic acid fermentation and SS removal of night soil wastewater are performed in the first stage, and UASB treatment is performed in the second stage, when external pH control is not performed, found that the liquid in the fermenter was maintained at a pH below 8.2, at which methane fermentation could occur, due to the residual presence of volatile organic acids in the subsequent UASB reaction.
以上の結果から、後段のUASBメタン発酵槽
にメタン発酵菌の栄養とならない無機酸を添加す
ることによりUASBメタン発酵槽におけるPHが
8.2以上に上昇することのないように制御するこ
とができれば、即ち、UASBメタン発酵槽にお
けるPHをいかなる場合においてもメタン発酵菌の
好ましいPH条件(PH6.9〜8.2)に保持できるよう
にすれば、揮発性有機酸の分解を促進し、処理液
中の揮発性有機酸濃度を低減しうるのではないか
と考えの下に種々検討を行つた。 From the above results, the pH in the UASB methane fermentation tank can be reduced by adding inorganic acids that do not provide nutrients to methane fermentation bacteria to the latter stage UASB methane fermentation tank.
If it can be controlled so that it does not rise above 8.2, that is, if the PH in the UASB methane fermenter can be maintained at the preferred PH conditions for methane fermenting bacteria (PH 6.9 to 8.2) in any case. We conducted various studies based on the idea that it might be possible to accelerate the decomposition of volatile organic acids and reduce the concentration of volatile organic acids in the processing liquid.
そして、添加すべき無機酸として炭酸ガスの利
用可能性について検討した。 Then, we investigated the possibility of using carbon dioxide gas as an inorganic acid to be added.
即ち、アンモニア性窒素濃度3000mg/のし尿
系汚水を発酵部容積2.0の上向流酸発酵槽に槽
容積1当り1.5の割合で30℃〜37℃の温度で
通液して酸発酵を行なわせると共に浮上したスカ
ムを除去して、SS含有量4500mg/の酸発酵液
を生成させ、これにPH6.5〜8.1となるように炭酸
ガスを圧入しながら発酵部容積2.0のUASB反
応槽に供給し通液速度3/日、温度30℃〜37℃
でメタン発酵を行なわせたところ、処理水中の揮
発性有機酸含有量120mg/で安定してメタン発
酵を行なうことができ、この場合のBOD除去率
は85%であつた。 That is, acid fermentation is carried out by passing human waste water with an ammonia nitrogen concentration of 3000 mg/into an upflow acid fermenter with a fermentation section volume of 2.0 at a rate of 1.5 per tank volume at a temperature of 30°C to 37°C. At the same time, the scum that floated up was removed to produce an acidic fermentation liquid with an SS content of 4500mg/, which was then fed to a UASB reaction tank with a fermentation section volume of 2.0 while pressurizing carbon dioxide gas to a pH of 6.5 to 8.1. Liquid flow rate 3/day, temperature 30℃~37℃
When methane fermentation was carried out in the treated water, methane fermentation could be carried out stably with a volatile organic acid content of 120 mg/in the treated water, and the BOD removal rate in this case was 85%.
なお、酸発酵液に炭酸ガスの圧入を行うことな
く同様にメタン発酵を行わせた場合、処理水中の
揮発性有機酸含有量2500mg/、BOD除去率68
%であつた。 In addition, when methane fermentation is performed in the same way without injecting carbon dioxide gas into the acid fermentation liquid, the volatile organic acid content in the treated water is 2500 mg/, and the BOD removal rate is 68.
It was %.
酸発酵槽又はメタン発酵槽で発生するガス中に
は多量の炭酸ガスが含まれており、このガスを後
段のUASB反応槽での反応後のPHの上昇防止の
ため酸発酵液中和剤として用いることができる。 The gas generated in the acid fermentation tank or methane fermentation tank contains a large amount of carbon dioxide gas, and this gas is used as a neutralizer for the acid fermentation liquid to prevent the pH from increasing after the reaction in the subsequent UASB reaction tank. Can be used.
即ち、酸発酵槽で発生したガスを酸発酵し尿に
循環通気し炭酸ガスを吸収せしめた後UASB法
によりメタン発酵せしめたところ、炭酸ガスを圧
入した場合と同様な結果が得られた。 That is, when the gas generated in the acid fermenter was circulated through acid-fermented human urine to absorb carbon dioxide gas, and then methane fermentation was carried out using the UASB method, results similar to those obtained when carbon dioxide gas was pressurized were obtained.
つぎに図面に基いて本発明を説明する。 Next, the present invention will be explained based on the drawings.
第1図は、本発明のし尿系汚水の処理装置を示
す概略フロー図であつて、酸発酵槽として、
UASB反応槽と同じ形の槽を用いた場合を示し
ている。 FIG. 1 is a schematic flow diagram showing the human waste wastewater treatment apparatus of the present invention, in which an acid fermenter is used as an acid fermenter.
This shows the case where a tank of the same shape as the UASB reaction tank is used.
し尿系汚水は、まず汚水導入管10からポンプ
4により酸発酵槽1の底部に設けられた分配流入
口6から酸発酵槽1に導入される。この酸発酵槽
においては主として酸発酵が進行するものである
が、メタン発酵も部分的に進行し、消化ガスを発
生する。発生したガスは酸発酵槽を上昇する際に
導入されたし尿系汚水中のSSに付着しSSを随伴
して浮上し、スカム層を形成する。形成されたス
カム層は酸発酵槽上部の気−固−液分離部7の水
面に設けられたスカムかき取り装置8によつて連
続的もしくは断続的に除去される。酸発酵槽に
は、冬期の如く気温・水温が低い時でもメタン発
酵が一部進行してガスの発生が行われるように、
し尿を25℃〜40℃に加温した後酸発酵槽に導入で
きるように加熱設備を設けておくのが好ましい。 Human waste wastewater is first introduced into the acid fermentation tank 1 from a waste water introduction pipe 10 by a pump 4 through a distribution inlet 6 provided at the bottom of the acid fermentation tank 1. In this acid fermenter, acid fermentation mainly proceeds, but methane fermentation also partially proceeds, generating digestive gas. The generated gas adheres to the SS in the human waste water introduced as it ascends through the acid fermentation tank, floats up with the SS, and forms a scum layer. The formed scum layer is continuously or intermittently removed by a scum scraping device 8 provided on the water surface of the gas-solid-liquid separation section 7 in the upper part of the acid fermenter. In the acid fermentation tank, even when the air and water temperatures are low, such as during the winter, methane fermentation partially proceeds and gas is generated.
It is preferable to provide heating equipment so that the human waste can be heated to 25°C to 40°C and then introduced into the acid fermentation tank.
酸発酵液は気−固−液分離部7の水面下より引
き出され炭酸ガス吸収装置3の下部へ導入され、
酸発酵槽の上部で分離された炭酸ガスを含むガス
をブロワー5から炭酸ガス吸収塔下部に設けた散
気管を通じて酸発酵液中に循環通気し、酸発酵液
に炭酸ガスを吸収せしめた後炭酸ガス吸収装置3
の上部から引き出し、UASBメタン発酵槽2の
底部に設けた分配流入管6よりUASBメタン発
酵槽2に導入し、上向流でメタン醗酵を行わせ
る。メタン発酵したし尿系汚水は、気−固−液分
離部7′で気体、固体、液体に分離され、気体は
中央部に集められ配管9′を経て引き出された後
メタンが分離される。一方処理液はメタン発酵槽
の上部から溢流し処理水排出樋11から排出さ
れ、分離された固体(主としてフロツク)は下方
に沈降せしめられる。 The acidic fermentation liquid is drawn out from below the water surface of the gas-solid-liquid separator 7 and introduced into the lower part of the carbon dioxide absorption device 3.
The gas containing carbon dioxide separated at the upper part of the acid fermentation tank is circulated and aerated into the acid fermentation liquor from the blower 5 through the aeration tube installed at the bottom of the carbon dioxide absorption tower, and after the acid fermentation liquor absorbs carbon dioxide gas, it is carbonated. Gas absorption device 3
It is pulled out from the top of the UASB methane fermentation tank 2, introduced into the UASB methane fermentation tank 2 through the distribution inflow pipe 6 provided at the bottom of the UASB methane fermentation tank 2, and methane fermentation is performed in an upward flow. The methane-fermented human waste water is separated into gas, solid, and liquid in the gas-solid-liquid separation section 7', and the gas is collected in the center and drawn out through the pipe 9', after which methane is separated. On the other hand, the treated liquid overflows from the upper part of the methane fermentation tank and is discharged from the treated water discharge gutter 11, and the separated solids (mainly flocs) are allowed to settle downward.
酸発酵槽1及びUASBメタン発酵槽は、共に
25℃〜40℃の温度に保つのが好ましく、また通液
量は各反応槽1当り0.5〜6/日の割合で
通液するのが好ましい。なお、通液量は夫々の発
酵槽の温度、し尿系汚水のBOD濃度或いは微生
物の活性等に基いて異なつていてもよい。 Acid fermenter 1 and UASB methane fermenter are both
It is preferable to maintain the temperature at 25° C. to 40° C., and the amount of liquid to be passed is preferably 0.5 to 6 per day per each reaction tank. Note that the amount of liquid passed may differ based on the temperature of each fermenter, the BOD concentration of human waste water, the activity of microorganisms, etc.
また、炭酸ガス吸収塔における炭酸ガス吸収量
はし尿系汚水のアンモニア性窒素の含有量により
異なるが、PH6.5〜8.1になる程度に吸収せしめる
のが好ましく、この為にはゲージ圧0.1〜5気圧
程度の加圧下に炭酸ガスを吸収せしめるのが好ま
しい。 The amount of carbon dioxide absorbed in the carbon dioxide absorption tower varies depending on the content of ammonia nitrogen in the human waste wastewater, but it is preferable to absorb the carbon dioxide to a pH of 6.5 to 8.1. It is preferable to absorb carbon dioxide gas under pressure of about atmospheric pressure.
本発明によるUASB反応槽を用いるし尿系汚
水処理の処理効率が改善された理由として、前記
のように処理水に残存する揮発性有機酸濃度を減
少せしめることができることの他に、UASB法
特有の改善効果がある。すなわち、高PHとそれに
よつて生じる遊離アンモニアの阻害作用によつ
て、UASB法がメタン発酵プロセスとして成立
するうえで最も重要なメタン菌によるグラニユー
ルの形成が十分になされないという欠点を克服で
きたことである。このことにはUASB法を採用
するうえできわめて重要な意義が存在する。PH中
和をなんら行なわずに酸発酵後のし尿系汚水を後
段のUASB反応槽に通水した場合には、処理開
始当初充填したグラニユール化汚泥は十分な活性
を維持しつつ保持されたが、少なくともそこでの
グラニユール化汚泥の増加が見られなかつた。し
たがつて、この方法によつては、処理装置運転の
始動に当たつて必らずグラニユール化したメタン
発酵汚泥を入手する必要があるがその入手のため
には相当の費用を必要とする。これに対して本発
明の方法では、当初充填したメタン発酵汚泥がグ
ラニユール化したものでなかつたにもかかわら
ず、後段UASB反応槽内において徐々にメタン
発酵汚泥のグラニユール化が進み、最終的にはPH
中和を行なわなかつたそれの3倍のグラニユール
化汚泥層が形成され、グラニユール化汚泥を用い
ることなくし尿処理用のUASBプロセスを始動
させることが可能であつた。また処理性能的に
は、炭酸ガス吸収によつてPH中和を行なわずに運
転した二段式し尿処理UASBプロセスの全滞留
時間が2.5日あつたのに対して、本発明の方法に
よつて達成できた全滞留時間は1.5日と、いずれ
もさらに高負荷、高速処理プロセス化することが
でき、また処理成積も前述のようにさらに優れた
ものであつた。このようなし尿系汚水の処理時間
は、従来実用されているし尿嫌気性消化槽のそれ
が平均30日であることと比較すれば、本発明の方
法は実に20倍〜30倍の高負荷処理、高速処理を達
成しうるものであり、その実用上の効果はきわめ
て大きいものである。 The reason why the treatment efficiency of night soil wastewater treatment using the UASB reaction tank according to the present invention has been improved is that, in addition to being able to reduce the concentration of volatile organic acids remaining in the treated water as described above, the It has an improving effect. In other words, due to the high pH and the resulting inhibitory effect of free ammonia, we were able to overcome the drawback that granule formation by methane bacteria, which is the most important factor for the UASB method to be established as a methane fermentation process, is not sufficiently achieved. It is. This has extremely important significance when adopting the UASB method. When the human waste water after acid fermentation was passed through the subsequent UASB reaction tank without any pH neutralization, the granulated sludge filled at the beginning of the treatment was retained with sufficient activity, but At least no increase in granulated sludge was observed there. Therefore, according to this method, it is necessary to obtain granulated methane fermentation sludge when starting up the operation of the treatment equipment, but obtaining it requires considerable expense. On the other hand, in the method of the present invention, although the methane fermentation sludge initially filled was not granulated, the methane fermentation sludge gradually progressed to granulation in the subsequent UASB reaction tank, and eventually PH
A granulated sludge layer three times larger than that without neutralization was formed, and it was possible to start up the UASB process for human waste treatment without using granulated sludge. In addition, in terms of treatment performance, the total residence time of the two-stage human waste treatment UASB process operated without PH neutralization by carbon dioxide gas absorption was 2.5 days, whereas the total residence time of the method of the present invention was 2.5 days. The total residence time achieved was 1.5 days, making it possible to achieve even higher load and faster treatment processes, and as mentioned above, the treatment yield was even more excellent. The processing time for such human waste wastewater is 20 to 30 times that of the conventional human waste anaerobic digester, which takes an average of 30 days. , it is possible to achieve high-speed processing, and its practical effects are extremely large.
第1図は、本発明のし尿系汚水処理装置の概略
を示すフロー図である。
1……酸発酵槽、2……UASBメタン発酵槽、
3……炭酸ガス吸収塔、6,6′……分配流入管、
7,7′……気−固−液分離部、9,9′……生成
ガス排出管、11……処理水排出樋。
FIG. 1 is a flow diagram schematically showing the human waste wastewater treatment apparatus of the present invention. 1... Acid fermenter, 2... UASB methane fermenter,
3... Carbon dioxide absorption tower, 6, 6'... Distribution inflow pipe,
7, 7'... Gas-solid-liquid separation section, 9, 9'... Produced gas discharge pipe, 11... Treated water discharge gutter.
Claims (1)
させると共に含有するSSをスカムとして除去し
た後、底部に分配流入管を、上部に気−固−液分
離部を有する汚泥床式メタン発酵反応槽中に上向
流で通水してメタン発酵処理を行なうに際し、酸
発酵槽からの流出液に炭酸ガスを吸収せしめた後
メタン発酵反応槽に供給することを特徴とするし
尿系汚水の処理方法。 2 炭酸ガスとして酸発酵槽で生成したガスを用
いる特許請求の範囲第1項記載のし尿系汚水の処
理方法。 3 炭酸ガスとしてメタン発酵槽で生成したガス
を用いる特許請求の範囲第1項記載のし尿系汚水
の処理方法。 4 底部にし尿系汚水の分配流入管を、上部に気
−固−液分離部並びに該気−固−液分離部に浮上
したスカムの除去装置を有している酸発酵槽と、
底部に前記酸発酵槽で生成した酸発酵液を導入す
るための分配流入管を、上部に気−固−液分離部
を有している汚泥床式メタン発酵槽とを連結して
なるし尿系汚水の処理装置において、酸発酵液を
メタン発酵槽の底部に導く配管上に酸発酵液に炭
酸ガスを吸収させる為の酸発酵液への炭酸ガス吸
収槽を設けたことを特徴とするし尿系汚水の処理
装置。 5 炭酸ガス吸収装置に、酸発酵槽で生成する炭
酸ガス含有ガスを導入するように配管してなる特
許請求の範囲第4項記載のし尿系汚水の処理装
置。 6 炭酸ガス吸収装置にメタン発酵槽で生成する
炭酸ガス含有ガスを導入するように配管してなる
特許請求の範囲第5項記載のし尿系汚水の処理装
置。[Scope of Claims] 1 Human waste wastewater is preliminarily fermented in an acid fermentation tank and the SS contained therein is removed as scum, and then the sludge has a distribution inflow pipe at the bottom and a gas-solid-liquid separation section at the top. When carrying out methane fermentation treatment by passing water in an upward flow through a bed type methane fermentation reaction tank, the method is characterized in that carbon dioxide gas is absorbed into the effluent from the acid fermentation tank and then supplied to the methane fermentation reaction tank. How to treat human waste water. 2. The method for treating human waste wastewater according to claim 1, which uses gas produced in an acid fermenter as the carbon dioxide gas. 3. The method for treating human waste wastewater according to claim 1, which uses gas produced in a methane fermentation tank as the carbon dioxide gas. 4. An acid fermenter having a distribution inflow pipe for human waste wastewater at the bottom, a gas-solid-liquid separation section and a removal device for scum floating in the gas-solid-liquid separation section at the top;
A night soil system in which a distribution inflow pipe for introducing the acid fermentation liquid produced in the acid fermentation tank at the bottom is connected to a sludge bed type methane fermentation tank having a gas-solid-liquid separation section at the top. A sewage treatment device, characterized in that a carbon dioxide gas absorption tank for the acid fermentation liquid is provided on the piping that leads the acid fermentation liquid to the bottom of the methane fermentation tank. Sewage treatment equipment. 5. The human waste sewage treatment device according to claim 4, wherein the carbon dioxide absorption device is piped to introduce the carbon dioxide-containing gas produced in the acid fermentation tank. 6. The human waste sewage treatment device according to claim 5, which is constructed by piping so as to introduce the carbon dioxide-containing gas produced in the methane fermentation tank into the carbon dioxide absorption device.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61123441A JPS62279899A (en) | 1986-05-30 | 1986-05-30 | Method and apparatus for treating sewage of excretion system |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61123441A JPS62279899A (en) | 1986-05-30 | 1986-05-30 | Method and apparatus for treating sewage of excretion system |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62279899A JPS62279899A (en) | 1987-12-04 |
| JPH0218915B2 true JPH0218915B2 (en) | 1990-04-27 |
Family
ID=14860673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61123441A Granted JPS62279899A (en) | 1986-05-30 | 1986-05-30 | Method and apparatus for treating sewage of excretion system |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62279899A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0547534U (en) * | 1991-12-02 | 1993-06-25 | 光洋精工株式会社 | Hydrodynamic bearing |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63287598A (en) * | 1987-05-21 | 1988-11-24 | Kajima Corp | Treatment of waste water |
| AU665241B2 (en) * | 1991-07-02 | 1995-12-21 | Ncs, Llc | Secondary sewage treatment system |
| JPH10118687A (en) * | 1996-10-22 | 1998-05-12 | Unitika Ltd | Treatment method of organic wastewater |
| JP4558231B2 (en) * | 2001-03-21 | 2010-10-06 | 三菱重工環境・化学エンジニアリング株式会社 | Method and system for treating liquid organic waste |
| JP2008221181A (en) * | 2007-03-15 | 2008-09-25 | Ebara Corp | Anaerobic treatment device and treatment method |
| KR100870425B1 (en) * | 2008-04-11 | 2008-11-25 | 한밭대학교 산학협력단 | Anaerobic Integrated Processing Equipment for Organic Waste Treatment |
| JP5731209B2 (en) * | 2011-01-24 | 2015-06-10 | 大阪瓦斯株式会社 | Method and apparatus for treating soap production waste liquid |
-
1986
- 1986-05-30 JP JP61123441A patent/JPS62279899A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0547534U (en) * | 1991-12-02 | 1993-06-25 | 光洋精工株式会社 | Hydrodynamic bearing |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62279899A (en) | 1987-12-04 |
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