JP3410866B2 - Treatment method of human wastewater - Google Patents
Treatment method of human wastewaterInfo
- Publication number
- JP3410866B2 JP3410866B2 JP18647695A JP18647695A JP3410866B2 JP 3410866 B2 JP3410866 B2 JP 3410866B2 JP 18647695 A JP18647695 A JP 18647695A JP 18647695 A JP18647695 A JP 18647695A JP 3410866 B2 JP3410866 B2 JP 3410866B2
- Authority
- JP
- Japan
- Prior art keywords
- photocatalyst
- activated carbon
- water
- sewage
- cod
- 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 - Fee Related
Links
- 238000000034 method Methods 0.000 title claims description 21
- 239000002351 wastewater Substances 0.000 title description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 52
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 51
- 239000011941 photocatalyst Substances 0.000 claims description 29
- 239000010865 sewage Substances 0.000 claims description 19
- 238000000926 separation method Methods 0.000 claims description 17
- 239000010800 human waste Substances 0.000 claims description 14
- 238000007254 oxidation reaction Methods 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 9
- 239000000701 coagulant Substances 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 4
- 230000001699 photocatalysis Effects 0.000 description 15
- 239000012528 membrane Substances 0.000 description 14
- 238000005345 coagulation Methods 0.000 description 10
- 230000015271 coagulation Effects 0.000 description 10
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000010419 fine particle Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 4
- 210000002700 urine Anatomy 0.000 description 4
- 238000007865 diluting Methods 0.000 description 3
- 238000013032 photocatalytic reaction Methods 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 230000001546 nitrifying effect Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical group [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 229940085991 phosphate ion Drugs 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 1
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- -1 centrifugation Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/30—Wastewater or sewage treatment systems using renewable energies
- Y02W10/37—Wastewater or sewage treatment systems using renewable energies using solar energy
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Physical Water Treatments (AREA)
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Water Treatment By Sorption (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明はし尿、浄化槽汚泥などの
し尿系汚水の処理方法に関し、特に光触媒を用いてし尿
系汚水を低コストで高度に浄化する方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for treating night soil sewage such as night sewage and septic tank sludge, and more particularly to a method for highly purifying night sewage wastewater using a photocatalyst at low cost.
【0002】[0002]
【従来の技術】現在最も進歩した処理方法は、し尿系汚
水を無希釈で生物学的硝化脱窒素したのちUF膜等で膜
分離し、膜透過水に無機凝集剤(硫酸アルミニウム、塩
化第2鉄など)を添加しリン、COD等を凝集除去し凝
集フロックを更にUF膜で膜分離し、膜透過水に残留す
るCODを粒状活性炭吸着して高度処理水とする方法で
ある。この技術はし尿系汚水の膜分離プロセスと呼ばれ
ている。2. Description of the Related Art The most advanced treatment method at present is to perform biological nitrification denitrification of undiluted human waste sewage undiluted and then perform membrane separation with a UF membrane or the like, and an inorganic coagulant (aluminum sulfate, second chloride (E.g. iron) to coagulate and remove phosphorus, COD, etc., further coagulate flocculated flocs with a UF membrane, and COD remaining in membrane permeated water is adsorbed on granular activated carbon to obtain highly treated water. This technology is called the membrane separation process of night soil wastewater.
【0003】[0003]
【発明が解決しようとする課題】しかし、従来のし尿系
汚水の膜分離プロセスは次のような問題点がある。
1.凝集処理によって除去できない低分子量CODが活
性炭処理工程にかなり多量に流入するため、活性炭のラ
ンニングコストが高い。
2.活性炭再生頻度が多くなり維持管理が煩雑である。
本発明の課題は、し尿系汚水の処理には従来適用された
ことがなかった光触媒による化学酸化手段を新規な態様
で適用しこれらの問題点を解決することである。However, the conventional membrane separation process for human waste water has the following problems. 1. Low-molecular-weight COD that cannot be removed by the coagulation treatment flows into the activated carbon treatment process in a considerably large amount, and thus the running cost of activated carbon is high. 2. The activated carbon is frequently regenerated and maintenance is complicated. An object of the present invention is to solve these problems by applying a photocatalytic chemical oxidation means that has never been applied to the treatment of night soil wastewater in a novel manner.
【0004】[0004]
【課題を解決するための手段】本発明の上記課題は、下
記構成により達成される。
(1)し尿系汚水を生物学的硝化脱窒素処理を含む工程
により処理する方法において、し尿系汚水を生物学的硝
化脱窒素処理したのち無機凝集剤により凝集分離し、該
凝集分離により得られた凝集分離水を光照射下で光触媒
と接触させ化学酸化を行ったのち、活性炭吸着すること
を特徴とするし尿系汚水の処理方法。
(2)前記凝集分離水に微粒子状の光触媒を添加懸濁さ
せ、光照射しながら化学酸化を行ったのち光触媒を固液
分離し、該固液分離により得られた分離水を活性炭吸着
する前記(1)記載のし尿系汚水の処理方法。The above object of the present invention can be achieved by the following constitution. (1) In a method of treating human waste sewage by a step including a biological nitrification denitrification treatment, the human sewage sewage is biologically nitrified and denitrified, and then coagulated and separated by an inorganic coagulant to obtain the coagulated separation. A method for treating human waste sewage, which comprises contacting aggregated separated water with a photocatalyst under light irradiation for chemical oxidation and then adsorbing activated carbon. (2) A particulate photocatalyst is added to and suspended in the aggregated separated water, chemically oxidized while being irradiated with light, and then the photocatalyst is subjected to solid-liquid separation, and the separated water obtained by the solid-liquid separation is adsorbed on activated carbon. (1) The method for treating human waste sewage as described above.
【0005】本発明技術思想の骨子は次の点である。
1.し尿系汚水を生物学的硝化脱窒素処理したのち無機
凝集剤により凝集分離し、該凝集分離により得られた凝
集分離水に対して酸化チタン、酸化カドミウム、酸化鉄
などの光触媒を接触させ光を照射し、化学酸化する。
2.光触媒処理して化学酸化した処理水を、更に活性炭
で処理する。
本発明の実施工程例を図1に示す。本発明における生物
学的硝化脱窒素処理は従来公知の方法を用いることがで
きる。本発明における生物学的硝化脱窒素処理は、し尿
系汚水を無希釈で行っても、適宜希釈して行ってもよい
が、のちに行う光触媒酸化反応の効率を考慮すると無希
釈で行うことが好ましい。また本発明の方法において、
し尿系汚水を生物学的硝化脱窒素処理するまえに、公知
の前処理等を行うことができる。本発明における生物学
的硝化脱窒素処理の後に行う凝集分離は、従来公知の方
法を用いることができる。該凝集分離に用いる無機凝集
剤としては従来公知のものを使用することができる。前
記凝集分離は、無機凝集剤の添加による凝集作用後沈
澱、遠心、膜分離のいかなる方法によっても良い。The main points of the technical idea of the present invention are as follows. 1. After biologically nitrifying and denitrifying the human waste sewage, it is coagulated and separated by an inorganic coagulant, and a photocatalyst such as titanium oxide, cadmium oxide, and iron oxide is brought into contact with the coagulated and separated water obtained by the coagulation and separation to emit light. Irradiate and chemically oxidize. 2. The treated water that has been subjected to photocatalytic treatment and chemical oxidation is further treated with activated carbon. FIG. 1 shows an example of steps for carrying out the present invention. For the biological nitrification denitrification treatment in the present invention, a conventionally known method can be used. The biological nitrification denitrification treatment in the present invention may be carried out without diluting the human waste sewage or appropriately diluting it, but it may be carried out neat in consideration of the efficiency of the photocatalytic oxidation reaction to be carried out later. preferable. In the method of the present invention,
Prior to biological nitrification and denitrification treatment of human waste sewage, a known pretreatment or the like can be performed. A conventionally known method can be used for coagulation separation performed after the biological nitrification denitrification treatment in the present invention. As the inorganic coagulant used for the coagulation separation, a conventionally known one can be used. The aggregation and separation may be performed by any method such as precipitation after aggregation action by adding an inorganic coagulant, centrifugation, and membrane separation.
【0006】[0006]
【作用】し尿系汚水を生物学的硝化脱窒素処理(以下、
単に生物処理ともいう)した処理水(以下、単に生物処
理水ともいう)を光触媒に接触させ光照射すると生物処
理水中のなんらかの物質が光触媒による化学酸化作用を
著しく妨害するが、生物処理水を凝集分離すると光触媒
効果の阻害因子が除去されCODが効果的に酸化分解す
ることが見いだされた。おそらく生物処理水中の光触媒
阻害物質は燐酸イオン、高分子量の有機物と推測され
る。(凝集処理によって燐酸イオン、高分子量有機物は
除去される)
またし尿系汚水を通常の活性汚泥法によってBODを除
去した後(窒素は除去されない)、凝集分離した処理水
を光触媒処理すると、凝集処理水中に多量のアンモニア
性窒素が残留しているため光触媒酸化反応がアンモニア
性窒素の硝酸化反応を優先的に生起させるためCOD除
去効果が著しく減少してしまうことが認められた。以上
の知見から光触媒による化学酸化を効果的に行なうには
し尿系汚水を生物学的に窒素を除去した後更に凝集処理
したものに対して光触媒処理を実施することが重要であ
ることが判明した。[Function] Biological nitrification and denitrification treatment of human waste system wastewater (hereinafter,
When treated water (also simply referred to as biologically treated water) (hereinafter also simply referred to as biologically treated water) is contacted with a photocatalyst and irradiated with light, some substance in the biologically treated water significantly interferes with the chemical oxidation action of the photocatalyst, but the biologically treated water aggregates. It was found that when separated, the inhibitor of photocatalytic effect was removed and COD was effectively oxidatively decomposed. Probably the photocatalytic inhibitor in the biologically treated water is phosphate ion, a high molecular weight organic substance. (Phosphate ion and high molecular weight organic matter are removed by coagulation treatment.) After removing BOD from urine-based wastewater by a normal activated sludge method (nitrogen is not removed), the treated water that has been coagulated and separated is subjected to a photocatalytic treatment. It was confirmed that the photocatalytic oxidation reaction preferentially causes the nitrification reaction of ammonia nitrogen because a large amount of ammonia nitrogen remains in the water, and the COD removal effect is significantly reduced. From the above findings, it was found that in order to effectively carry out chemical oxidation by photocatalyst, it is important to perform photocatalytic treatment on the urine system wastewater after biological nitrogen removal and further coagulation treatment. .
【0007】光触媒酸化反応によるCOD除去速度はか
なり小さいので一日以上の反応時間を設けるのが好まし
い。光触媒作用を発揮させるには紫外線照射ランプでも
当然可能であるが電力、紫外線ランプ交換などランニン
グコストが著しく高くなるので極力低コストで処理する
必要があるし尿処理にはあまり実用的でなく、太陽光を
利用することが好ましい。例えばし尿処理施設の屋上、
または屋外に池を設け太陽光を照射しながら凝集処理水
が長時間滞留できるようにし充分光触媒反応を進行させ
るようにする方法が好適である。池の水深はあまり深く
すると太陽光の照射不足を招くので50cm程度とするこ
とが好ましい。勿論、建設費的に余裕があれば集光機と
光ファイバー導光体、放散体の組合せにより太陽光をよ
り深い水中に導入することを妨げない。またし尿系汚水
に多量の希釈水を添加して生物処理すると水量が増加し
光触媒反応槽の容量が大きくなりすぎ実際上実施困難に
なるので理想的には無希釈生物処理することが望まし
い。Since the rate of COD removal by the photocatalytic oxidation reaction is quite low, it is preferable to provide a reaction time of one day or longer. It is naturally possible to use a UV irradiation lamp to exert the photocatalytic action, but since running costs such as electric power and UV lamp replacement are extremely high, it is necessary to treat at a low cost as much as possible and it is not very practical for urine treatment. Is preferably used. For example, the roof of a human waste treatment facility,
Alternatively, a method in which a pond is provided outdoors so that the coagulated water can be retained for a long time while irradiating sunlight to allow the photocatalytic reaction to proceed sufficiently is preferable. If the water depth of the pond is too deep, the irradiation of sunlight will be insufficient, so it is preferable to set it to about 50 cm. Of course, if the construction cost is affordable, the combination of the condenser, the optical fiber light guide, and the diffuser will not prevent the introduction of sunlight into deeper water. Further, if a large amount of diluting water is added to urine-based wastewater for biological treatment, the amount of water increases and the capacity of the photocatalytic reaction tank becomes too large to be practically practical. Therefore, ideally, undiluted biological treatment is desirable.
【0008】しかしながら太陽光を用いると、冬季、雨
天時、夜間に光触媒反応による効果が減少、消失するの
で安定して良好な処理水質が得られないという欠点があ
るが、本発明はこの欠点を次のように解決した。すなわ
ち太陽光による光触媒処理水を更に活性炭吸着処理する
ことにより、冬季、雨天時、夜間にはCODが高い水が
活性炭工程に供給され活性炭によりこのCODが除去さ
れ、太陽光が十分に照射される時間帯はCODがほとん
ど含まれない水が活性炭工程に供給されることになり常
に安定して良好な処理水を得られる。この結果年間平均
の活性炭へのCOD負荷量も従来法(凝集処理水を活性
炭処理する方法)より大きく減少できる。上記のよう
に、し尿系汚水を生物学的硝化脱窒素処理した後に凝集
分離を行い、次いで該凝集分離により得られた凝集分離
水を光触媒酸化反応を行い、更に該光触媒酸化反応によ
り得られた光触媒処理水を活性炭処理するという概念は
従来全くなかったものである。However, when sunlight is used, the effect of photocatalytic reaction decreases and disappears in winter, in the rain, and at night, so that stable treated water quality cannot be obtained, but the present invention has this drawback. It was solved as follows. That is, by further subjecting the photocatalyst-treated water by sunlight to adsorption of activated carbon, water with high COD is supplied to the activated carbon process in winter, rainy weather, and night, and this COD is removed by activated carbon, so that sunlight is sufficiently irradiated. During the time period, water containing almost no COD is supplied to the activated carbon process, and stable, good treated water can always be obtained. As a result, the annual average COD load on activated carbon can be greatly reduced as compared with the conventional method (method of treating coagulated water with activated carbon). As described above, the human wastewater was biologically nitrified and denitrified, and then coagulated and separated, and then the coagulated and separated water obtained by the coagulation and separation was subjected to a photocatalytic oxidation reaction and further obtained by the photocatalytic oxidation reaction. The concept of treating photocatalyst-treated water with activated carbon has never existed before.
【0009】光触媒の形状としては微粒子状、粒状担体
に光触媒を付着させたもの、板状もしくは、棒状物の表
面に光触媒を付着させたものなど公知のものを利用でき
る。光触媒を担体に固定化すると光触媒の表面積が減少
し反応速度が減少することがあるので、その場合は光触
媒を微粒子状のままで凝集分離水に懸濁して使用するの
がよい。微粒子状光触媒の凝集分離水への懸濁濃度は5
00〜20000mg/l程度で良く、好ましくは1000
〜5000mg/l程度とすると良い。光触媒微粒子は凝集
ろ過、UF膜などのろ過手段により分離回収し再利用す
る。光触媒の経時的な劣化はほとんど認められないが、
触媒能力を保証するため年間10%程度の光触媒の補給
ができるようにしておくのが好ましい。As the shape of the photocatalyst, known ones such as fine particles, those having a photocatalyst attached to a granular carrier, and those having a photocatalyst attached to the surface of a plate-shaped or rod-shaped material can be used. When the photocatalyst is immobilized on the carrier, the surface area of the photocatalyst may be reduced and the reaction rate may be reduced. In that case, it is preferable to suspend the photocatalyst in the form of fine particles in the aggregated water for use. The suspension concentration of the particulate photocatalyst in the aggregated water is 5
It may be about 2000 to 20000 mg / l, preferably 1000
It is recommended to set it up to about 5000 mg / l. The photocatalyst fine particles are separated and collected by a filtration means such as coagulation filtration or a UF membrane and reused. Almost no deterioration of the photocatalyst over time is observed,
It is preferable that about 10% of the photocatalyst can be replenished annually in order to guarantee the catalytic ability.
【0010】[0010]
【実施例】以下に、本発明を実施例を用いてさらに詳細
に説明するが、本発明はこの実施例により制限されるも
のではない。
〔実施例1〕し尿を無希釈で生物学的硝化脱窒素した処
理水(以下生物処理水と言う)を実施設(静岡県F市)
から採取し本発明方法により試験を行ない本発明効果を
検証した。生物処理水(COD530mg/l、色度280
0)に塩化第2鉄を1500mg/l添加し凝集分離した処
理水(COD92mg/l、色度120)に酸化チタン光触
媒粉末(富士チタン(株)製,粒径0.15〜0.3μ
m,アナターゼ型の結晶型を持つもの)を5000mg/l
添加懸濁させ、晴天時の屋外に設置した水深50cmの槽
に2日間滞留させたのち、UF膜(日東電工(株)製、
公称分画分子量10000)で酸化チタン微粒子を分離
した。このUF膜透過水はCOD11mg/l、色度8)で
あった。これを粒状活性炭吸着カラムに空間速度(S
V)2で通水したところ、カラム流出水はCOD3mg/
l、色度0であった。次に雨天時に同様の実験を行なっ
た結果、光触媒処理後のUF膜透過水のCODは43mg
/l、色度40)であり放流水質基準(COD15mg/l以
下)を満足できなかったが、UF膜透過水の活性炭処理
水はCOD8mg/l、色度2であった。以上の条件で1年
間(雨天時合計112日)連続試験を行なった結果、活
性炭流入水の平均CODは22mg/lであった。活性炭処
理水は6カ月通水後もCOD15mg/l以下を維持し、こ
の間活性炭再生は不要であった。EXAMPLES The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples. Example 1 Treated water obtained by biologically nitrifying and denitrifying human sewage undiluted (hereinafter referred to as biologically treated water) was installed (F city, Shizuoka prefecture).
Then, the test was conducted by the method of the present invention to verify the effect of the present invention. Biologically treated water (COD 530 mg / l, chromaticity 280
(1) 1500 mg / l of ferric chloride was added to 0), and treated water (COD 92 mg / l, chromaticity 120) obtained by coagulation and separation was added to titanium oxide photocatalyst powder (manufactured by Fuji Titanium Co., Ltd., particle size 0.15 to 0.3 μ).
m, having anatase type crystal type) 5000 mg / l
After adding and suspending it, it was allowed to stay in a tank with a water depth of 50 cm installed outdoors during fine weather for 2 days, and then a UF membrane (manufactured by Nitto Denko Corporation,
The titanium oxide fine particles were separated with a nominal molecular weight cutoff of 10,000). This UF membrane permeated water had a COD of 11 mg / l and a chromaticity of 8). The space velocity (S
V) 2 was passed, the column effluent was COD 3 mg /
The chromaticity was 1 and the chromaticity was 0. Next, when the same experiment was performed in rainy weather, the COD of the UF membrane permeation water after the photocatalytic treatment was 43 mg.
/ l, chromaticity 40), which did not satisfy the discharge water quality standard (COD 15 mg / l or less), but the activated carbon treated water of the UF membrane permeate had COD 8 mg / l and chromaticity 2. As a result of conducting a continuous test for 1 year (total 112 days in rainy weather) under the above conditions, the average COD of the activated carbon inflow water was 22 mg / l. The COD of the activated carbon-treated water remained below 15 mg / l even after passing through the water for 6 months, and regeneration of the activated carbon was unnecessary during this period.
【0011】〔比較例1〕前記実施例1の凝集分離した
処理水(COD92mg/l)を光触媒処理することなく直
接活性炭処理(SV2)したところ20日後の活性炭処
理水はCOD18mg/lに悪化し20日に1度の活性炭再
生が必要であった。
〔比較例2〕前記実施例1の生物処理水(COD530
mg/l、リン632mg/l)に直接、実施例1に使用したも
のと同じ酸化チタン光触媒を10000mg/l添加し、晴
天時の屋外に2日間滞留させたのち膜分離したところ、
膜透過水CODは495mg/lでありほとんどCODが除
去されなかった。このことから、生物処理後凝集分離さ
せたものを光触媒酸化処理することが重要であることが
わかる。[Comparative Example 1] The treated water (COD 92 mg / l) which had been coagulated and separated in Example 1 was directly treated with activated carbon (SV2) without photocatalyst treatment. The activated carbon treated water after 20 days deteriorated to COD 18 mg / l. It was necessary to regenerate the activated carbon once every 20 days. [Comparative Example 2] The biologically treated water of Example 1 (COD530
The same titanium oxide photocatalyst as used in Example 1 was directly added to 10000 mg / l, phosphorus 632 mg / l), and the mixture was allowed to stand for 2 days outdoors in fine weather and then subjected to membrane separation,
The membrane permeated water COD was 495 mg / l, and almost no COD was removed. From this, it is understood that it is important to photocatalyst-oxidize the product that has been aggregated and separated after the biological treatment.
【0012】[0012]
【発明の効果】し尿系汚水を、生物学的硝化脱窒素処
理、無機凝集剤による凝集分離、光触媒酸化反応、活性
炭吸着の順で行うことにより、以下の効果が得られた。
1.活性炭の再生頻度がおよそ1/6に減少する。
2.太陽光を利用する場合、夜間、雨天時に光触媒の効
果が大きく減少するが、この際も問題なく、常に良好な
処理水が得られる。
3.紫外線照射ランプが不要にできるので維持管理コス
トが安価である。
4.生物処理水を凝集分離することにより光触媒を阻害
する物質を除去することができ光触媒作用を効果的に発
揮させることが可能である。
また、光触媒として微粒子状のものを用いることによ
り、CODの化学酸化をさらに効率のよく行うことがで
きる。The following effects were obtained by performing the biological nitrification denitrification treatment, the coagulation separation with the inorganic coagulant, the photocatalytic oxidation reaction, and the activated carbon adsorption on the human waste sewage in this order. 1. The regeneration frequency of activated carbon is reduced to about 1/6. 2. When sunlight is used, the effect of the photocatalyst is greatly reduced at night and in rainy weather, but in this case as well, good treated water can always be obtained. 3. The maintenance cost is low because the ultraviolet irradiation lamp can be eliminated. 4. By coagulating and separating the biologically treated water, the substance that inhibits the photocatalyst can be removed, and the photocatalytic action can be effectively exhibited. Further, by using the photocatalyst in the form of fine particles, COD can be chemically oxidized more efficiently.
【図1】本発明の実施工程例を示す。FIG. 1 shows an example of steps for carrying out the present invention.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI C02F 9/00 503 C02F 9/00 503D 504 504A 504E 1/28 1/28 D 1/32 1/32 1/52 1/52 E 3/34 101 3/34 101A (56)参考文献 特開 昭64−75098(JP,A) 特開 昭55−44361(JP,A) 特開 昭53−16454(JP,A) 特開 昭63−214398(JP,A) 特開 平2−172597(JP,A) (58)調査した分野(Int.Cl.7,DB名) C02F 9/00 501 C02F 9/00 502 C02F 1/28 C02F 1/32 C02F 1/52 C02F 3/34 101 ─────────────────────────────────────────────────── ─── Continued Front Page (51) Int.Cl. 7 Identification Code FI C02F 9/00 503 C02F 9/00 503D 504 504A 504E 1/28 1/28 D 1/32 1/32 1/52 1/52 E 3/34 101 3/34 101A (56) Reference JP-A 64-75098 (JP, A) JP-A 55-44361 (JP, A) JP-A 53-16454 (JP, A) JP-A 63-214398 (JP, A) JP-A-2-172597 (JP, A) (58) Fields investigated (Int.Cl. 7 , DB name) C02F 9/00 501 C02F 9/00 502 C02F 1/28 C02F 1/32 C02F 1/52 C02F 3/34 101
Claims (2)
含む工程により処理する方法において、し尿系汚水を生
物学的硝化脱窒素処理したのち無機凝集剤により凝集分
離し、該凝集分離により得られた凝集分離水を光照射下
で光触媒と接触させ化学酸化を行ったのち、活性炭吸着
することを特徴とするし尿系汚水の処理方法。1. A method for treating human waste sewage by a step including a biological nitrification denitrification treatment, wherein the human sewage sewage is subjected to biological nitrification denitrification treatment, and then coagulated and separated by an inorganic coagulant. A method for treating human waste sewage, characterized in that the obtained aggregated and separated water is brought into contact with a photocatalyst under light irradiation for chemical oxidation and then activated carbon is adsorbed.
加懸濁させ、光照射しながら化学酸化を行ったのち光触
媒を固液分離し、該固液分離により得られた分離水を活
性炭吸着する請求項1記載のし尿系汚水の処理方法。2. A particulate photocatalyst is added to and suspended in the aggregated separated water, chemically oxidized while being irradiated with light, and then the photocatalyst is subjected to solid-liquid separation, and the separated water obtained by the solid-liquid separation is adsorbed on activated carbon. The method for treating human waste sewage according to claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18647695A JP3410866B2 (en) | 1995-06-30 | 1995-06-30 | Treatment method of human wastewater |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18647695A JP3410866B2 (en) | 1995-06-30 | 1995-06-30 | Treatment method of human wastewater |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0910799A JPH0910799A (en) | 1997-01-14 |
| JP3410866B2 true JP3410866B2 (en) | 2003-05-26 |
Family
ID=16189154
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18647695A Expired - Fee Related JP3410866B2 (en) | 1995-06-30 | 1995-06-30 | Treatment method of human wastewater |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3410866B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100461894B1 (en) * | 2002-12-09 | 2004-12-17 | 김용남 | Sewage and waste water disposal plant |
| CN102951722B (en) * | 2011-08-31 | 2014-04-02 | 成都易生玄科技有限公司 | Method for treating drinking water comprehensively by collecting sunlight and bamboo charcoals |
| CN104211256A (en) * | 2014-08-26 | 2014-12-17 | 常州大学 | COD biofilm-photocatalytic device in micro-polluted water |
-
1995
- 1995-06-30 JP JP18647695A patent/JP3410866B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0910799A (en) | 1997-01-14 |
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