JPH0470080B2 - - Google Patents
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- Publication number
- JPH0470080B2 JPH0470080B2 JP63233641A JP23364188A JPH0470080B2 JP H0470080 B2 JPH0470080 B2 JP H0470080B2 JP 63233641 A JP63233641 A JP 63233641A JP 23364188 A JP23364188 A JP 23364188A JP H0470080 B2 JPH0470080 B2 JP H0470080B2
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- anaerobic
- anaerobic digestion
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
- C04B35/634—Polymers
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3205—Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
- C04B2235/3206—Magnesium oxides or oxide-forming salts thereof
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3418—Silicon oxide, silicic acids or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/52—Constituents or additives characterised by their shapes
- C04B2235/5208—Fibers
- C04B2235/5212—Organic
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/54—Particle size related information
- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5427—Particle size related information expressed by the size of the particles or aggregates thereof millimeter or submillimeter sized, i.e. larger than 0,1 mm
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/54—Particle size related information
- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5436—Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
-
- 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
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Ceramic Engineering (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Treatment Of Sludge (AREA)
Description
〔産業上の利用分野〕
本発明は、下水汚泥、農水産廃棄物等の有機性
汚泥の処理方法に関するものである。
〔従来の技術〕
下水処理場における都市下水の標準的な微生物
処理においては、下水まずは曝気槽で好気的微生
物処理され、その後、沈殿槽に送られる。沈殿槽
から排出される上澄みは二次的な処理工程に送ら
れ、一方、沈殿した大量の汚泥すなわち余剰汚泥
は、濃縮後、焼却されたり廃棄されたりすること
もあるが、脱水、焼却が困難な性状であるばかり
か、廃棄処分には病原性微生物を撤散らして環境
を悪化させるという問題もあるので、処分する前
になるべくその量を減らす処理を施す必要があ
る。そのための処理方法の代表的なものは、嫌気
性消化処理であつて、嫌気性微生物の代謝を利用
して有機物を有機酸、メタンガス、炭酸ガス等に
分解する。しかしながら、余剰汚泥は微生物の塊
のようなものであつてきわめて分解しにくいか
ら、その嫌気性消化に要する日数は、中温消化
(温度35〜37℃)の場合で20〜30日と長い。しか
も、それだけの日数を費やしても有機物の分解率
は40〜50%程度にとどまり、したがつて排出液は
依然として高濃度の有機物を含有し、その後の水
処理の大きな負担となつている。
〔発明が解決しようとする課題〕
上述のように、従来の汚泥処理法は能率が悪
く、そのため大型の嫌気性消化槽を必要とし、固
形物の減量効果も満足できるものではなかつた。
また、排出される水は有機物濃度が高く、到底そ
のまま放流できるものではないし、さらに処理す
るとしても大きな負担となるものであつた。
そこで本発明は、従来の汚泥処理法における上
述の問題点を解決し、より短時日でより高率の減
量と有機物と分解を達成できる汚泥処理法を提供
しようとするものである。
〔課題を解決するための手段〕
本発明が提供する汚泥処理法は、有機性汚泥に
そのPHが9〜11になるまでアルカリを添加して汚
泥中の微生物菌体の可溶化を生じさせ、さらに湿
式ミル処理により残存微生物菌体等を破砕し、処
理後の汚泥にPH9〜11で滞留日数2〜5日の嫌気
性消化処理を施し、該嫌気性消化処理後の汚泥か
ら分離されたアルカリ性の水を好アルカリ性微細
藻類により好気性消化処理することを特徴とす
る。
以下、本発明の汚泥処理法について更に詳しく
説明する。
汚泥のアルカリ処理は、カ性ソーダ、炭酸ソー
ダ等のアルカリを汚泥PHが9〜11になるまで加
え、温度約20〜30℃で0.5〜1時間程度保持する
ことにより行う。これにより、汚泥中の微生物の
細胞壁が破壊され、蛋白質、糖などの細胞内成分
が溶出するいわゆる可溶化が起こる。PH11以上の
強アルカリ性にすることは、可溶化促進には有効
でも、後の嫌気性消化工程においてそのような強
アルカリ性の汚泥中で増殖するメタン菌の十分量
を消化槽内に蓄積させることなどが困難になるの
で、好ましくない。
アルカリ処理した汚泥をさらに湿式ミル処理す
る。この湿式ミル処理は、水中に懸濁している固
形物に主として剪断摩擦力を作用させることによ
り固形物の微細化を行う処理であつて、具体的に
は、回転円筒式ミル、振動ボールミル、遠心式ボ
ールミル、媒体撹拌式ミル、コロイドミル等を用
いて高度の摩砕をを行うものである。湿式ミル処
理の中でも、媒体撹拌式ミルは処理効果の点で最
もすぐれているので、特に好ましい。この媒体撹
拌式ミルは、円筒状容器に挿入した撹拌用デイス
クを高速で回転させることによつて容器内のビー
ズを激しく撹拌し、ビース間に剪断摩擦力が生じ
させて摩砕を行うものであつて、用途に応じて大
小様々なビーズが使われるが、汚泥可溶化に好ま
しいビーズは、粒径が0.05〜1mmのものである。
その場合、撹拌用デイスクの回転数は1000〜
3000rpm(周速10〜30m/sec)程度、被処理汚泥
の滞留時間は通常の汚泥を処理する場合で5〜60
分程度が適当である。
アルカリ処理によつて可溶化しなかつた微生物
細胞や繊維質の有機物も、この湿式ミル処理によ
つて可溶化し、あるいは嫌気性消化を受け易い形
態に破砕されする。湿式ミル処理だけでも可溶化
や破砕は可能であるが、アルカリ処理によつて膨
潤し一部可溶化した汚泥構成成分に対しては、湿
式ミル処理の効果は一層顕著に且つ短時間に現れ
る。
湿式ミル処理を施した後の汚泥の嫌気性消化処
理は、単一の嫌気性消化槽において、次のように
して行う。汚泥は、アルカリ処理を受けているこ
とにより強いアルカリ性であるが、必要に応じて
さらにアルカリを加え、PH9〜11の状態で嫌気性
消化槽に供給する。あるいは、消化槽に継続的に
アルカリを注入して、槽内を上記PHに保つ。通
常、下水汚泥中のメタン菌の増殖に好適なPHは8
未満の弱アルカリ性とされており、特に酸生成菌
とメタン菌とを共存させる単一槽消化の場合のPH
は、従来、調整する場合も無調整の場合も7前後
であるから、本発明の消化法においてPHは従来よ
りもかなり高い値に設定される。本発明の消化法
においては、PHがこのように高い値であることに
より、第一に汚泥成分の可溶化がさらに進み、嫌
気性微生物による消化を受け易い状態になる。第
二に、病原性微生物が全く検出されないまでに死
滅する。
上述のようにPHが高い状態の汚泥中の旺盛に増
殖する好アルカリ性メタン菌は、通常の下水汚泥
や従来の嫌気性消化槽からの消化汚泥の中には少
ないが、嫌気性消化槽の運転開始に当たり槽内PH
を9〜11に維持して行う馴養期間を設けることに
より、槽内嫌気性菌菌叢の大部分を占めるものと
することができる。
馴養により好アルカリ性嫌気性菌群が準備され
たならば、消化槽に被処理汚泥を供給して正常運
転としての嫌気性消化を開始する。この処理にお
いて、槽内温度は特に限定されるものではない
が、30〜40℃が適当であり、また滞留日数は2〜
5日とする。滞留日数がこれより長すぎると、槽
内メタン菌のうち好アルカリ性メタン菌の占める
割合が低下し、消化率の低下を招く。
嫌気性消化槽から排出された汚泥は、固液を分
離した後、そのまま適宜処分することもできる
が、本発明の処理法においては、液相部分につい
てさらに好アルカリ性微細藻類による好気的消化
処理を行う。処理には、滞留日数として4〜10日
を要する。この処理は、アルカリ処理および湿式
ミル処理により可溶化した有機物のうち嫌気性微
生物によつて分解されなかつたものを上記藻類の
栄養源として利用させることにより、排水中の有
機物含有量を減少させるもので、用いる藻類とし
ては、スピルリナ、アナベナなど、後で分離し易
い大型微細藻類が適当である。この処理で特に好
アルカリ性藻類を用いる理由は、強いアルカリ性
で行われた嫌気性消化槽からの排水を中和するこ
となしに処理でき、また雑菌増殖の恐れが少な
く、培養管理が容易だからである。
以上、余剰汚泥を処理する場合について本発明
を説明したが、本発明の処理法は、下水処理場に
おいて発生する他の汚泥の処理にも好適であるこ
とは勿論、製あんなど農水産加工工場からの廃棄
物、家畜糞尿、畜体処理廃棄物、魚腸骨などの廃
棄処理する場合にも適用可能である。
〔実施例〕
都市下水処理場より採取した余剰汚泥および混
合汚泥(余剰汚泥と初沈汚泥との1:1混合物)
について、本発明による処理とその比較実験を行
なつた。汚泥の組成および実験条件は次のとおり
である。
汚泥組成:
TS(%) VS(%)
余剰汚泥 4.0 3.0
混合汚泥 3.8 3.1
アルカリ処理条件:
25%カ性ソーダ溶液を汚泥PHが10になるまで
添加し、常温で30分間攪拌する。
湿式ミル処理条件:
使用装置:媒体攪拌式ミル・パールミル(アシ
ザワ株式会社、型式PM1STS、ビーズ径0.2
mm、デイスク回転数1300rpm、周速度6m/
sec
滞留時間:5分
嫌気性消化条件:
5容フアーメンターを使用、300rpmで連
続攪拌し、かつPHコントローラでPHを10に維持
する。
消化温度:37℃
滞留日数:2日
実験開始時馴養:下水処理場から採取した中温消
化汚泥を最初の種汚泥に用いて次のように実施
最初の2週間:滞留日数10日
次の2週間:滞留日数5日
最後の2週間:滞留日数2日
好アルカリ性藻類による処理:
使用藻類:スピルリナ(Spirulina sp.)
滞留日数:4日
培養槽:容量25、液深5cm、PH10
500Wフラツドランプで液面を照度10Kluxに
証明
比較のために、アルカリ処理および湿式ミル処
理を全く行わずに嫌気性消化および好アルカリ性
藻類による消化処理を行なつた実験(比較例1)
および湿式ミル処理のみを行いアルカリ処理を行
わないほかは上記と同様にした実験(比較例2)
を行なつた。
嫌気性消化槽の馴養終了後10日間、嫌気性消化
槽における消化率(VS除去率)、ガス発生量、ガ
スのメタン含有率および揮発性有機酸量を測定
し、さらに、藻類による消化処理における消化
率、揮発性有機酸量および窒素含量(遠心分離上
澄液)の測定を行なつた。測定値の平均値を表1
および表2に示す。
[Industrial Application Field] The present invention relates to a method for treating organic sludge such as sewage sludge and agricultural and fishery waste. [Prior Art] In standard microbial treatment of municipal sewage at a sewage treatment plant, sewage is first subjected to aerobic microbial treatment in an aeration tank, and then sent to a settling tank. The supernatant discharged from the settling tank is sent to a secondary treatment process, while the large amount of settled sludge, or surplus sludge, is sometimes incinerated or disposed of after thickening, but it is difficult to dewater and incinerate it. Not only do they have dangerous properties, but disposal also poses the problem of dispersing pathogenic microorganisms and degrading the environment, so it is necessary to take steps to reduce the amount as much as possible before disposal. A typical treatment method for this purpose is anaerobic digestion, in which organic matter is decomposed into organic acids, methane gas, carbon dioxide gas, etc. using the metabolism of anaerobic microorganisms. However, excess sludge is like a mass of microorganisms and is extremely difficult to decompose, so the number of days required for anaerobic digestion is as long as 20 to 30 days in the case of mesophilic digestion (temperature of 35 to 37°C). Moreover, even after spending that many days, the decomposition rate of organic matter remains at about 40 to 50%, so the effluent still contains a high concentration of organic matter, which poses a heavy burden for subsequent water treatment. [Problems to be Solved by the Invention] As mentioned above, the conventional sludge treatment method is inefficient, requires a large anaerobic digestion tank, and has an unsatisfactory solids reduction effect.
In addition, the discharged water has a high concentration of organic matter, so it cannot be discharged as is, and even if it were to be further treated, it would be a heavy burden. Therefore, the present invention aims to solve the above-mentioned problems in conventional sludge treatment methods and to provide a sludge treatment method that can achieve a higher rate of weight loss and decomposition of organic matter in a shorter period of time. [Means for Solving the Problems] The sludge treatment method provided by the present invention includes adding alkali to organic sludge until its pH becomes 9 to 11 to cause solubilization of microbial cells in the sludge, Furthermore, residual microbial cells etc. are crushed by wet milling, and the treated sludge is subjected to anaerobic digestion treatment at pH 9 to 11 for a retention period of 2 to 5 days. It is characterized by subjecting water to aerobic digestion treatment using alkaliphilic microalgae. Hereinafter, the sludge treatment method of the present invention will be explained in more detail. Alkali treatment of sludge is carried out by adding an alkali such as caustic soda or soda carbonate until the pH of the sludge reaches 9 to 11, and maintaining the mixture at a temperature of about 20 to 30°C for about 0.5 to 1 hour. This destroys the cell walls of microorganisms in the sludge and causes so-called solubilization, in which intracellular components such as proteins and sugars are eluted. Although making the sludge strongly alkaline to PH11 or above is effective in promoting solubilization, it may cause a sufficient amount of methane bacteria to accumulate in the digester, which grows in such strongly alkaline sludge during the subsequent anaerobic digestion process. This is not desirable because it becomes difficult. The alkali-treated sludge is further subjected to wet mill treatment. This wet milling process is a process in which solids are pulverized by mainly applying shearing frictional force to the solids suspended in water. A high degree of grinding is performed using a type ball mill, a media stirring type mill, a colloid mill, etc. Among the wet milling methods, the media agitation mill is particularly preferred since it has the best processing effect. This media stirring type mill violently stirs the beads in the container by rotating a stirring disk inserted into a cylindrical container at high speed, creating a shearing friction force between the beads and grinding them. Beads of various sizes are used depending on the purpose, but beads with a particle size of 0.05 to 1 mm are preferred for solubilizing sludge.
In that case, the rotation speed of the stirring disk should be 1000~
Approximately 3000 rpm (peripheral speed 10 to 30 m/sec), the residence time of the sludge to be treated is 5 to 60 when treating normal sludge.
About a minute is appropriate. Microbial cells and fibrous organic matter that were not solubilized by the alkali treatment are also solubilized by this wet mill treatment or crushed into a form that is susceptible to anaerobic digestion. Although solubilization and crushing can be achieved by wet milling alone, the effects of wet milling are more pronounced and appear in a shorter time for sludge constituents that have swelled and been partially solubilized by alkali treatment. Anaerobic digestion of sludge after wet milling is carried out in a single anaerobic digestion tank as follows. The sludge is strongly alkaline due to the alkali treatment, but if necessary, alkali is added to the sludge and the sludge is supplied to the anaerobic digestion tank at a pH of 9 to 11. Alternatively, alkali is continuously injected into the digestion tank to keep the inside of the tank at the above pH. Normally, the optimum pH for the growth of methane bacteria in sewage sludge is 8.
It is said to be weakly alkaline, with a PH of less than
Conventionally, pH is around 7 both when adjusted and when not adjusted, so in the digestion method of the present invention, the pH is set to a much higher value than conventionally. In the digestion method of the present invention, due to such a high pH value, firstly, the solubilization of the sludge components further progresses, making them susceptible to digestion by anaerobic microorganisms. Second, pathogenic microorganisms are killed off to the point where they are no longer detectable. As mentioned above, alkaliphilic methane bacteria, which proliferate vigorously in sludge with a high pH, are rare in normal sewage sludge and digested sludge from conventional anaerobic digestion tanks, but when operating an anaerobic digestion tank, Tank pH at start
By providing an acclimatization period in which the anaerobic bacterial flora is maintained at 9 to 11, the anaerobic bacteria can occupy the majority of the anaerobic bacterial flora in the tank. Once the alkaliphilic anaerobic bacteria group is prepared by acclimatization, the sludge to be treated is supplied to the digestion tank and anaerobic digestion is started as normal operation. In this treatment, the temperature inside the tank is not particularly limited, but 30 to 40℃ is appropriate, and the residence time is 2 to 40℃.
It will be 5 days. If the retention period is too long, the proportion of alkaliphilic methane bacteria among the methane bacteria in the tank will decrease, leading to a decrease in digestibility. The sludge discharged from the anaerobic digestion tank can be appropriately disposed of as it is after separating the solid and liquid, but in the treatment method of the present invention, the liquid phase portion is further subjected to aerobic digestion treatment using alkaliphilic microalgae. I do. The treatment requires a residence time of 4 to 10 days. This treatment reduces the content of organic matter in wastewater by using the organic matter that has been solubilized through alkali treatment and wet milling that has not been decomposed by anaerobic microorganisms as a nutrient source for the algae. Suitable algae to be used are macroscopic microalgae that can be easily separated later, such as Spirulina and Anabaena. The reason why alkaliphilic algae is particularly used in this treatment is that it can treat wastewater from an anaerobic digestion tank that has been subjected to strong alkalinity without neutralizing it, there is little fear of bacterial growth, and culture management is easy. . The present invention has been described above for the case of treating surplus sludge, but the treatment method of the present invention is of course suitable for treating other sludge generated in sewage treatment plants, as well as in agricultural and fishery processing plants such as mills. It can also be applied to the disposal of waste from animals, livestock manure, livestock processing waste, fish iliac bones, etc. [Example] Surplus sludge and mixed sludge collected from a city sewage treatment plant (1:1 mixture of surplus sludge and initial settling sludge)
For this purpose, treatment according to the present invention and comparative experiments were conducted. The composition of the sludge and the experimental conditions are as follows. Sludge composition: TS (%) VS (%) Surplus sludge 4.0 3.0 Mixed sludge 3.8 3.1 Alkaline treatment conditions: Add 25% caustic soda solution until the sludge pH reaches 10 and stir for 30 minutes at room temperature. Wet mill processing conditions: Equipment used: Media stirring type pearl mill (Ashizawa Co., Ltd., model PM1STS, bead diameter 0.2
mm, disc rotation speed 1300 rpm, peripheral speed 6 m/
sec Residence time: 5 minutes Anaerobic digestion conditions: Use a 5 volume fermenter, continuously stir at 300 rpm, and maintain PH at 10 with a PH controller. Digestion temperature: 37℃ Residence days: 2 days Acclimatization at the start of the experiment: Mesophilic digested sludge collected from a sewage treatment plant was used as the initial seed sludge and carried out as follows First 2 weeks: Residence days 10 days Next 2 weeks : Retention days: 5 days Last 2 weeks: Residence days: 2 days Treatment with alkaliphilic algae: Algae used: Spirulina (Spirulina sp.) Residence days: 4 days Culture tank: Capacity 25, liquid depth 5 cm, PH10 500W flat lamp to lower the liquid level For comparison, an experiment was conducted in which anaerobic digestion and alkaliphilic algae digestion were performed without any alkali treatment or wet mill treatment (Comparative Example 1)
and an experiment similar to the above except that only wet mill treatment was performed and no alkali treatment was performed (Comparative Example 2)
I did this. For 10 days after the acclimatization of the anaerobic digester, we measured the digestibility (VS removal rate), gas generation amount, methane content of gas, and volatile organic acid content in the anaerobic digester, and also measured the VS removal rate in the anaerobic digester. Digestibility, volatile organic acid content and nitrogen content (centrifugation supernatant) were measured. Table 1 shows the average values of the measured values.
and shown in Table 2.
【表】【table】
本発明の汚泥処理法によれば、上述のように極
めて短時間で従来の最高の水準と同等またはそれ
以上の高い消化率を嫌気性消化工程において達成
し、汚泥量を顕著に減少させることができるとと
もに、排出水の水質も良好にすることができる。
したがつて、従来と比べて消化槽の単位体積当た
りの処理能力の大幅な向上、あるいは消化槽の著
しい小型化が可能となるとともに、消化汚泥発生
量が減少してその後処理が容易となるという、顕
著な効果が奏される。また、強いアルカリ性で処
理されていることにより、嫌気性消化槽から排出
される消化汚泥は病原性微生物を含まないだけで
なく、その中に残つている嫌気性微生物が強いア
ルカリ性で増殖したものであつて自然界に放出さ
れると大部分死滅してしまうものであるため、消
化汚泥を廃棄したとき環境を汚染する恐れが少な
いという利点がある。
According to the sludge treatment method of the present invention, as described above, a high digestibility equal to or higher than the highest conventional level can be achieved in the anaerobic digestion process in an extremely short period of time, and the amount of sludge can be significantly reduced. At the same time, the quality of the waste water can also be improved.
Therefore, compared to conventional systems, it is possible to significantly improve the processing capacity per unit volume of the digester, or make the digester significantly smaller, and the amount of digested sludge generated is reduced, making subsequent treatment easier. , a remarkable effect is achieved. In addition, because the sludge is treated with strong alkalinity, the digested sludge discharged from the anaerobic digestion tank not only does not contain pathogenic microorganisms, but also contains the remaining anaerobic microorganisms that have grown in the strong alkalinity. Since most of the digested sludge will die if it is released into the natural world, it has the advantage that there is little risk of contaminating the environment when it is disposed of.
Claims (1)
リを添加して汚泥中の微生物菌体の可溶化を生じ
させ、さらに湿式ミル処理により残存微生物菌体
等を破砕し、処理後の汚泥にPH9〜11で滞留日数
2〜5日の嫌気性消化処理を施し、該嫌気性消化
処理後の汚泥から分離されたアルカリ性の水を好
アルカリ性微細藻類により好気性消化処理するこ
とを特徴とする汚泥の処理方法。1. Add alkali to organic sludge until its pH reaches 9 to 11 to solubilize the microbial cells in the sludge, and then use a wet mill to crush remaining microbial cells, and add the remaining microbial cells to the treated sludge. A sludge characterized by subjecting the sludge to an anaerobic digestion treatment at a pH of 9 to 11 for a retention period of 2 to 5 days, and subjecting alkaline water separated from the sludge after the anaerobic digestion treatment to an aerobic digestion treatment using alkaliphilic microalgae. processing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63233641A JPH0283098A (en) | 1988-09-20 | 1988-09-20 | Treatment of sludge |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63233641A JPH0283098A (en) | 1988-09-20 | 1988-09-20 | Treatment of sludge |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0283098A JPH0283098A (en) | 1990-03-23 |
| JPH0470080B2 true JPH0470080B2 (en) | 1992-11-09 |
Family
ID=16958226
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63233641A Granted JPH0283098A (en) | 1988-09-20 | 1988-09-20 | Treatment of sludge |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0283098A (en) |
-
1988
- 1988-09-20 JP JP63233641A patent/JPH0283098A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0283098A (en) | 1990-03-23 |
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