JPS644840B2 - - Google Patents
Info
- Publication number
- JPS644840B2 JPS644840B2 JP55122850A JP12285080A JPS644840B2 JP S644840 B2 JPS644840 B2 JP S644840B2 JP 55122850 A JP55122850 A JP 55122850A JP 12285080 A JP12285080 A JP 12285080A JP S644840 B2 JPS644840 B2 JP S644840B2
- Authority
- JP
- Japan
- Prior art keywords
- digestion
- temperature
- low
- reactor
- main
- 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
- 230000029087 digestion Effects 0.000 claims description 48
- 238000000034 method Methods 0.000 claims description 35
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 28
- 239000010815 organic waste Substances 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 description 22
- 239000005416 organic matter Substances 0.000 description 12
- 239000010802 sludge Substances 0.000 description 12
- 239000002699 waste material Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000000354 decomposition reaction Methods 0.000 description 7
- 238000000926 separation method Methods 0.000 description 6
- 239000010801 sewage sludge Substances 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000013585 weight reducing agent Substances 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000003795 desorption Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 244000144972 livestock Species 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000010170 biological method Methods 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 239000000110 cooling liquid Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- CMMUKUYEPRGBFB-UHFFFAOYSA-L dichromic acid Chemical compound O[Cr](=O)(=O)O[Cr](O)(=O)=O CMMUKUYEPRGBFB-UHFFFAOYSA-L 0.000 description 1
- 239000005446 dissolved organic matter Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000010800 human waste Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 230000007483 microbial process Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000011197 physicochemical method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 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
- 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
- Treatment Of Sludge (AREA)
Description
本願発明は、下水汚泥、都市廃棄物、農畜産廃
棄物などの有機性廃棄物からメタンを生成回収す
るとともに、これら有機性廃棄物を軽量・安定化
させる嫌気性消化法に関するものである。
下水汚泥、都市廃棄物、農畜産廃棄物などの有
機性廃棄物の発生量は今日増加の一途にあり、こ
れらの処理処分に関しては環境保護の観点から重
大な関心が寄せられている。他方、近年エネルギ
ー需要の逼迫状況を背景に、廃棄物処理について
は効率的であると同時にエネルギー消費の少な
い、出来ることならエネルギーの回収可能な方法
が望まれている。このような状況を背景に、有機
性廃棄物を減量・安定化させる過程でメタンが生
成回収できる嫌気性消化法が注目され始めてい
る。
嫌気性消化法は、何種類もの嫌気性微生物群が
有機物に作用して有機物を最終的にCH4、CO2、
H2O、NH4 +などの比較的簡単な構造の物質に分
離することを原理としているが、より詳細には、
この分解反応は次の3種の微生物反応が逐次的に
進行して生ずる反応であると把握されている。
(1) 低分子化反応
高分子有機物→低分子有機物
(2) 揮発酸生成反応
低分子有機物→揮発酸、アルコール
H2、CO2、NH4 +
(3) メタン生成反応
揮発酸、アルコール
H2、CO2→CH4
CO2
このような有機物の分解反応は、一般的には非
常に緩慢に進行し、このため従来主として下水汚
泥やし尿などの処理に利用されてきた標準的な嫌
気性消化法では、反応器の滞留時間すなわち消化
日数を30日と非常に長くとつており、これが嫌気
性消化法の欠点としてあげられている。従来よ
り、このような分解反応全体を律速する反応は最
終段のメタン生成反応と考えられてきたが、下水
汚泥、都市廃棄物、農畜産廃棄物など固形物性の
有機性廃棄物を対象とした場合には、むしろ第1
段の低分子化反応が律速段階になることが明らか
にされ、この反応を促進する技術が幾つか提案さ
れている。これらの技術は、大別すれば熱、薬品
(アルカリ、酸)などを加えて原廃棄物に前処理
を施す物理化学的方法と、主消化工程とは別個の
微生物工程を設け、そこで強力な低分子化作用を
持つ微生物を繁殖せしめる生物的方法に分けられ
るが、経済性からみれば後者の方が優れている。
本発明者らは、これ迄提案されてきた生成物低
分子化法を追実験して検討した結果、45℃〜65℃
で活動する高温性かつ嫌気性の低分子化菌を利用
した低分子化法が極めて有効であることを確認し
た。また、従来このような高温低分子化菌を低分
子化工程で利用する場合には、後段の主消化工程
も同様の高温域に維持する高温消化法を採用する
のが常であつた。本発明者らも、当初は高温低分
子化法−高温消化法の組合わせで実験を行つた
が、排出される消化汚泥は固液分離離性に乏し
く、また固液分離後の脱離液には高濃度のコロイ
ド状溶解性有機物が含まれ、汚泥処理、廃液処理
を含めた実用技術としては難点が多いことが明ら
かになつた。そこで、低分子化工程からの流出液
を強制的に冷却して後段の主消化工程を20℃〜40
℃に中温消化法に切換えて運転を継続したとこ
ろ、前記難点が大幅に改善されるばかりでなく、
メタン発生量、有機性分解率もかえつて高くなる
ことが確認された。
このように、本発明は有機性廃棄物の嫌気性消
化法の問題点を解消し、低分子化反応の速度の増
大と、得られる消化汚泥の固液分離性の向上が可
能な方法を提供することを目的とし、上記実験結
果に基づいて完成されたものである。
すなわち、本発明は有機性廃棄物を嫌気性消化
処理するに際し、少なくとも工程を二分割し、前
記有機性廃棄物を第一工程の低分子化工程にて45
℃〜65℃の高温域消化温度で低分子化処理したの
ち該処理物を冷却し、第二工程の主消化工程にて
20℃〜40℃の中温域消化温度で嫌気性消化処理す
ることを特徴とする有機性廃棄物の嫌気性消化方
法である。
本願発明の実施態様の一例を第1図に従つて説
明すると、廃棄物6(これは物理化学的前処理を
受けた廃棄物でもよい)は、45℃〜65℃の範囲に
制御された低分子化反応器1に流入する。この低
分子化反応器1としては、従来の生物処理に用い
られる槽型反応器、固定床反応器、流動床反応器
のいずれでもよく、要は廃棄物6と高温性低分子
化菌がよく接触でき、実質的に嫌気性条件が維持
できる構造であればよい。なお、流出スラリー7
に含まれる低分子化反応用の微生物を利用するた
めに、固液分離装置4を用いて流出スラリー7を
脱離液8と固形物9に分離し、固形物9の一部を
低分子化反応器1へ返送してもよい。(固形物9
の殆どは後記の主消化反応器2に送られる。)
固液分離装置4からの脱離液8は、温度が20℃
〜40℃に維持されている主消化反応器2に流入す
る。この主消化反応器2としては、低分子化反応
器1と同様に槽型、固定床型、流動床型など様々
な反応器が適用できるが、いずれにせよ低分子化
工程以上に厳しい嫌気性条件が必要になるので、
その密閉性に十分な配慮が拡われた構造でなけれ
ばならない。また、この図例では主消化工程を単
一工程としているが、必要により、これを酸生成
工程と、その後段のメタン生成工程などに細分し
て複数の工程にする変法も可能である。
主消化反応器2からの消化汚泥10はこのまま
処分してもよいが、実用上は沈殿濃縮槽、遠心分
離機、その他の固液分離装置5により処理され、
脱離液11と沈殿物12に分離される。脱離液1
1は別途に処理され、沈殿物12は焼却などによ
つて処分される。この場合、所望により沈殿物1
2の一部を主消化反応器2に返送してもよい。
本発明においては、低分子化反応器1からの流
出スラリー7の液温が主消化反応器2内で制御さ
れるべき液温よりもかなり高いので、流出スラリ
ー7は冷却する必要がある。この場合、熱交換器
3で廃棄物6により冷却するのが合理的で好まし
い。
次に、本発明を完成するために行つた実験方法
及び結果の一例を実施例としてあげ、あわせて従
来法と比べた本発明の効果を明らかにする。
実施例
実験装置は、第2図のごとく主要機器として槽
内液量3の低分子化槽1′と槽内液量6(い
ずれも撹拌機付き)の主消化槽2′を含むもので
あり、これらはそれぞれ恒温水槽13,16内に
セツトされ、個別に槽内液温が制御できるように
なつている。第2図中、3′は熱交換器、14は
パルプ粉末の投入口、15は熱交換器3′内の冷
却用液体の冷却装置、17はガス計量器である。
しかして、廃棄物としての下水汚泥6′とパル
プ粉末は低分子化槽1′で低分子有機物となり、
流出スラリー7′は熱交換器3′を経て主消化槽
2′に流入して消化され、スラリー状の消化汚泥
10′となつて排出される。低分子化槽1′及び主
消化槽2′で発生するメタン含有ガス18はガス
計量器17により、その発生量と組成が計測され
る。
次に実験条件について記すと、まず温度条件
は、低分子化槽1′の槽内液温を55℃(高温低分
子化)と33℃(中温低分子化)の2種類に、また
主消化槽2′の槽内液温を55℃(高温消化)と33
℃(中温消化)の2種類にそれぞれ設定し、高
温低分子化−中温消化(本発明法)、高温低分
子化−高温消化(比較例1)、中温低分子化
(比較例2)、中温低分子化−中温消化(比較例
3)の4通りについて実験した。
一方、模擬廃棄物としてはパルプ粉末と有機物
濃度2.5%の下水汚泥を使用し、これらの供給量
(処理量)は1日当たりそれぞれ45g、600mlとし
た。反応器内の滞留時間は、低分子化槽1′は5
日、主消化槽2′は10日とした。したがつて実験
装置全体(前記両反応器の合計容量)に対する有
機物負荷は約6.7Kg/m3・日である。このような
負荷条件で、前記4通りについてそれぞれ運転を
行つた。それぞれの実験におけるメタン含有ガス
18の発生量、そのメタン含率、メタン発生量
と、消化汚泥10′の有機物濃度の平均値から計
算した有機物分解率は第1表のとおりであつた。
次に、得られた消化汚泥10′の脱水テストを、
日本下水道協会発行「下水試験法」1974年版のヌ
ツチエ式脱水試験に準じて行つた。
すなわち、消化汚泥10′の乾燥固形物量に対
して消石灰10%、FeCl35%を添加混合し、面積
35cm2のリーフで真空度400mmHgで過して求めた
比抵抗の平均値は第1表のとおりになつた。
また11500Gで遠心分離した上清澄液(第1図
における脱離液11に相当する)の重クロム酸
COD値の平均値は第1表のとおりであつた。
The present invention relates to an anaerobic digestion method that generates and recovers methane from organic wastes such as sewage sludge, municipal waste, agricultural and livestock waste, and also makes these organic wastes lightweight and stable. The amount of organic wastes such as sewage sludge, municipal wastes, and agricultural and livestock wastes being generated continues to increase these days, and the treatment and disposal of these wastes is of great concern from the perspective of environmental protection. On the other hand, with the recent tightening of energy demand, there is a desire for efficient waste treatment methods that consume less energy and, if possible, can recover energy. Against this background, anaerobic digestion methods, which generate and recover methane during the process of reducing and stabilizing organic waste, are beginning to attract attention. In the anaerobic digestion method, many types of anaerobic microorganisms act on organic matter to finally convert it into CH 4 , CO 2 ,
The principle is to separate substances with relatively simple structures such as H 2 O and NH 4 + , but in more detail,
It is understood that this decomposition reaction is caused by the following three types of microbial reactions proceeding sequentially. (1) Low-molecular-weight organic matter → Low-molecular-weight organic matter (2) Volatile acid production reaction Low-molecular organic matter → Volatile acid, alcohol H 2 , CO 2 , NH 4 + (3) Methane production reaction Volatile acid, alcohol H 2 , CO 2 → CH 4 CO 2This kind of decomposition reaction of organic matter generally proceeds very slowly, so standard anaerobic digestion, which has traditionally been used primarily to treat sewage sludge and human waste, In this method, the residence time in the reactor, that is, the number of days for digestion, is extremely long at 30 days, and this is cited as a drawback of the anaerobic digestion method. Conventionally, the rate-limiting reaction of the entire decomposition reaction has been thought to be the final step, the methane production reaction. In some cases, the first
It has been revealed that the molecular weight reduction reaction is the rate-determining step, and several techniques have been proposed to accelerate this reaction. These technologies can be roughly divided into physicochemical methods in which raw waste is pretreated by adding heat, chemicals (alkali, acids), etc., and microbial processes that are separate from the main digestion process, in which a powerful It can be divided into biological methods that propagate microorganisms that have the effect of reducing molecular weight, but the latter is superior from an economic standpoint. As a result of additional experiments and studies on the methods for reducing the molecular weight of products that have been proposed so far, the present inventors found that
We have confirmed that the low-molecular-weighting method using high-temperature, anaerobic low-molecular-weight bacteria that is active in the environment is extremely effective. Furthermore, conventionally, when such high-temperature low-molecular-weight bacteria were used in the low-molecular-weighting process, a high-temperature digestion method was usually employed in which the subsequent main digestion process was also maintained at a similar high temperature range. The present inventors also initially conducted experiments using a combination of high-temperature low-molecularization method and high-temperature digestion method, but the digested sludge discharged had poor solid-liquid separation properties, and the desorbed sludge after solid-liquid separation contains high concentrations of colloidal dissolved organic matter, and it has become clear that there are many difficulties in practical technology including sludge treatment and waste liquid treatment. Therefore, we forcibly cooled the effluent from the low-molecular-weighting process and heated the latter main digestion process to 20°C to 40°C.
When we switched to the mesophilic digestion method and continued operation, not only did the above-mentioned difficulties improve significantly, but we also
It was confirmed that the amount of methane generated and the rate of organic decomposition increased. As described above, the present invention solves the problems of anaerobic digestion of organic waste, and provides a method that can increase the speed of the molecular weight reduction reaction and improve the solid-liquid separability of the resulting digested sludge. It was completed based on the above experimental results. That is, the present invention divides the process into at least two parts when subjecting organic waste to anaerobic digestion, and converts the organic waste into 45
After being subjected to low-molecularization treatment at a high-temperature digestion temperature range of ℃ to 65℃, the treated product is cooled and then processed in the main digestion step of the second step.
This is an anaerobic digestion method for organic waste, which is characterized by anaerobic digestion treatment at a meso-temperature digestion temperature of 20°C to 40°C. An example of the embodiment of the present invention will be described with reference to FIG. It flows into the molecularization reactor 1. The low-molecular-weight reactor 1 may be a tank reactor, a fixed bed reactor, or a fluidized bed reactor used in conventional biological treatment. Any structure is sufficient as long as it can be contacted and maintain substantially anaerobic conditions. In addition, the spilled slurry 7
In order to utilize the microorganisms for the low-molecular-weight reaction contained in It may be returned to reactor 1. (Solid matter 9
Most of it is sent to the main digestion reactor 2, which will be described later. ) The temperature of the desorbed liquid 8 from the solid-liquid separator 4 is 20°C.
It flows into the main digestion reactor 2 which is maintained at ~40°C. As this main digestion reactor 2, various reactors such as tank type, fixed bed type, fluidized bed type, etc. can be applied like the low molecular weight reactor 1, but in any case, the anaerobic reaction is more severe than the low molecular weight process. Conditions are required, so
The structure must be designed with sufficient consideration given to its airtightness. Further, in this example, the main digestion step is a single step, but if necessary, it is possible to subdivide this into a plurality of steps, such as an acid production step and a subsequent methane production step. The digested sludge 10 from the main digestion reactor 2 may be disposed of as is, but in practice it is treated with a sedimentation concentration tank, a centrifuge, or other solid-liquid separation device 5.
It is separated into a desorbed liquid 11 and a precipitate 12. Desorption liquid 1
1 is treated separately, and the precipitate 12 is disposed of by incineration or the like. In this case, if desired, the precipitate 1
2 may be returned to the main digestion reactor 2. In the present invention, the outflow slurry 7 needs to be cooled because the temperature of the outflow slurry 7 from the depolymerization reactor 1 is considerably higher than the liquid temperature to be controlled in the main digestion reactor 2. In this case, it is reasonable and preferable to cool the heat exchanger 3 with the waste 6. Next, an example of the experimental method and results carried out to complete the present invention will be given as an example, and the effects of the present invention in comparison with conventional methods will also be clarified. Example As shown in Fig. 2, the experimental equipment includes a low-molecular-weighting tank 1' with an internal liquid volume of 3 and a main digestion tank 2' with an internal liquid volume of 6 (both equipped with a stirrer) as main equipment. These are set in constant temperature water tanks 13 and 16, respectively, so that the temperature of the liquid in the tank can be controlled individually. In FIG. 2, 3' is a heat exchanger, 14 is a pulp powder inlet, 15 is a cooling device for cooling liquid in the heat exchanger 3', and 17 is a gas meter. Thus, the waste sewage sludge 6' and pulp powder become low-molecular organic matter in the low-molecular conversion tank 1'.
The effluent slurry 7' flows into the main digestion tank 2' through the heat exchanger 3', is digested, and is discharged as slurry-like digested sludge 10'. A gas meter 17 measures the amount and composition of the methane-containing gas 18 generated in the low molecular weight tank 1' and the main digestion tank 2'. Next, regarding the experimental conditions, first, the temperature conditions were two types: the liquid temperature in the low molecularization tank 1' was 55℃ (high temperature low molecularization) and 33℃ (medium temperature low molecularization), and the main digestion The liquid temperature in tank 2' was set to 55℃ (high temperature digestion) and 33℃.
℃ (medium-temperature digestion), high-temperature low-molecularization-medium-temperature digestion (method of the present invention), high-temperature low-molecularization-high-temperature digestion (comparative example 1), medium-temperature low molecularization (comparative example 2), and medium-temperature Experiments were conducted on four methods: low molecular weight reduction and mesothermal digestion (Comparative Example 3). On the other hand, pulp powder and sewage sludge with an organic matter concentration of 2.5% were used as simulated wastes, and the supply amounts (processing amounts) of these were 45 g and 600 ml per day, respectively. The residence time in the reactor is 5
The main digester 2' was used for 10 days. Therefore, the organic load on the entire experimental apparatus (total capacity of both reactors) was approximately 6.7 Kg/m 3 ·day. Under such load conditions, each of the four types described above was operated. Table 1 shows the organic matter decomposition rate calculated from the amount of methane-containing gas 18 generated, its methane content, the amount of methane generated, and the average value of the organic matter concentration of the digested sludge 10' in each experiment. Next, the obtained digested sludge 10' was subjected to a dehydration test.
The test was carried out in accordance with the Nutsuchie dehydration test published by the Japan Sewage Works Association, 1974 edition of ``Sewage Testing Methods''. That is, 10% slaked lime and 5% FeCl 3 are added and mixed to the dry solid content of 10' of digested sludge, and the area is
Table 1 shows the average values of resistivity determined by passing through a 35 cm 2 leaf at a vacuum degree of 400 mmHg. In addition, dichromic acid of the supernatant liquid (corresponding to desorbed liquid 11 in Figure 1) centrifuged at 11500G
The average COD values were as shown in Table 1.
【表】
第1表を見て明らかなように、本発明法は各比
較例と比べて有機物分解率、メタン発生量は高
く、かつ消化汚泥の固液分離性、脱水性が極めて
優れていることが確認された。
従来法−12300mg/
本発明法−3800 〃
以上述べたように、本発明によれば、低分子化
工程と主消化工程における消化温度を制御するこ
とにより、消化汚泥の固液分離性、脱水性が大幅
に改善でき、したがつて、脱水ケーキの処分が容
易になり、脱水分離水の廃水処理が著しく合理化
されと共に、有機物の消化に要する日数も短縮で
き、有機物の分解率、メタン発生量等は従来法と
同等又はそれ以上であり、また、消化設備も簡
単、安価で済むなどの利点が得られる。[Table] As is clear from Table 1, the method of the present invention has a higher organic matter decomposition rate and higher methane generation than each comparative example, and is extremely superior in solid-liquid separation and dewatering properties of digested sludge. This was confirmed. Conventional method - 12,300 mg / Inventive method - 3,800 As described above, according to the present invention, by controlling the digestion temperature in the low molecularization process and the main digestion process, the solid-liquid separation property and dewatering property of digested sludge can be improved. Therefore, the disposal of the dehydrated cake becomes easier, the wastewater treatment of the dehydrated separated water is significantly streamlined, and the number of days required to digest organic matter can be shortened, and the decomposition rate of organic matter, amount of methane generated, etc. is equivalent to or better than the conventional method, and has the advantage that the digestion equipment is simple and inexpensive.
第1図、第2図は、それぞれ本発明の実施態
様、実施例を示す系統説明図である。
1……低分子化反応器、1′……低分子化槽、
2……主消化反応器、2′……主消化槽、3,
3′……熱交換器、4,5……固液分離装置、6
……廃棄物、6′……下水汚泥、7,7′……流出
スラリー、8……脱離液、9……固形物、10,
10′……消化汚泥、11……脱離液、12……
沈殿物、13……恒温水槽、14……パルプ粉末
投入口、15……冷却装置、16……恒温水槽、
17……ガス計量器、18……メタン含有ガス。
FIG. 1 and FIG. 2 are system explanatory diagrams showing embodiments and examples of the present invention, respectively. 1... Low molecular weight reactor, 1'... Low molecular weight tank,
2... Main digestion reactor, 2'... Main digestion tank, 3,
3'... Heat exchanger, 4, 5... Solid-liquid separation device, 6
...Waste, 6'...Sewage sludge, 7,7'...Effluent slurry, 8...Desorbed liquid, 9...Solid matter, 10,
10'... Digested sludge, 11... Desorption liquid, 12...
Sediment, 13... constant temperature water tank, 14... pulp powder inlet, 15... cooling device, 16... constant temperature water tank,
17...Gas meter, 18...Methane-containing gas.
Claims (1)
少なくとも工程を二分割し、前記有機性廃棄物を
第一工程の低分子化工程にて45℃〜65℃の高温域
消化温度で低分子化処理したのち該処理物を冷却
し、第二工程の主消化工程にて20℃〜40℃の中温
域消化温度で嫌気性消化処理することを特徴とす
る有機性廃棄物の嫌気性消化法。 2 前記主消化工程が酸生成工程と、その後段の
メタン生成工程に分割してなるものである特許請
求の範囲第1項記載の消化法。[Claims] 1. In anaerobic digestion of organic waste,
The process is divided into at least two parts, and the organic waste is subjected to a low-molecularization process at a high temperature digestion temperature range of 45°C to 65°C in the first process, and then the treated product is cooled, and then the second process is performed. An anaerobic digestion method for organic waste, characterized in that anaerobic digestion is carried out at a meso-temperature digestion temperature of 20°C to 40°C in the main digestion step. 2. The digestion method according to claim 1, wherein the main digestion step is divided into an acid production step and a subsequent methane production step.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55122850A JPS5748396A (en) | 1980-09-04 | 1980-09-04 | Anaerobic digestion of organic waste matter |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55122850A JPS5748396A (en) | 1980-09-04 | 1980-09-04 | Anaerobic digestion of organic waste matter |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5748396A JPS5748396A (en) | 1982-03-19 |
| JPS644840B2 true JPS644840B2 (en) | 1989-01-26 |
Family
ID=14846177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55122850A Granted JPS5748396A (en) | 1980-09-04 | 1980-09-04 | Anaerobic digestion of organic waste matter |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5748396A (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003326237A (en) * | 2002-03-05 | 2003-11-18 | Osaka Gas Co Ltd | Organic waste treatment system |
| JP3820216B2 (en) * | 2002-12-20 | 2006-09-13 | 三菱重工業株式会社 | Operation method of medium temperature digester |
| WO2007083456A1 (en) * | 2006-01-20 | 2007-07-26 | Kurita Water Industries Ltd. | Method and apparatus for anaerobic digestion treatment of organic waste liquid |
| ES2828665T3 (en) * | 2010-04-12 | 2021-05-27 | Seab Power Ltd | Portable renewable energy microgeneration system |
| WO2025243975A1 (en) * | 2024-05-22 | 2025-11-27 | 本田技研工業株式会社 | Organic matter treatment apparatus, organic matter treatment method, and method for producing fuel gas |
-
1980
- 1980-09-04 JP JP55122850A patent/JPS5748396A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5748396A (en) | 1982-03-19 |
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