JPS6041594A - Treatment of organic waste liquid - Google Patents
Treatment of organic waste liquidInfo
- Publication number
- JPS6041594A JPS6041594A JP58149620A JP14962083A JPS6041594A JP S6041594 A JPS6041594 A JP S6041594A JP 58149620 A JP58149620 A JP 58149620A JP 14962083 A JP14962083 A JP 14962083A JP S6041594 A JPS6041594 A JP S6041594A
- Authority
- JP
- Japan
- Prior art keywords
- sludge
- tank
- anaerobic
- liquid
- phosphorus
- 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.)
- Granted
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 51
- 239000010815 organic waste Substances 0.000 title claims description 8
- 239000010802 sludge Substances 0.000 claims abstract description 119
- 238000005273 aeration Methods 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 26
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 239000007789 gas Substances 0.000 claims description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 13
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims 1
- 229910017604 nitric acid Inorganic materials 0.000 claims 1
- 150000002826 nitrites Chemical class 0.000 claims 1
- 238000001556 precipitation Methods 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract description 46
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 46
- 239000011574 phosphorus Substances 0.000 abstract description 46
- 230000005484 gravity Effects 0.000 abstract description 10
- 239000006228 supernatant Substances 0.000 abstract description 9
- 230000003247 decreasing effect Effects 0.000 abstract description 3
- 229910002651 NO3 Inorganic materials 0.000 abstract description 2
- 238000010521 absorption reaction Methods 0.000 abstract description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 abstract 1
- 230000008719 thickening Effects 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000000126 substance Substances 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000010865 sewage Substances 0.000 description 5
- 239000005416 organic matter Substances 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 235000009984 Pterocarpus indicus Nutrition 0.000 description 2
- 241000533793 Tipuana tipu Species 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- UKUVVAMSXXBMRX-UHFFFAOYSA-N 2,4,5-trithia-1,3-diarsabicyclo[1.1.1]pentane Chemical compound S1[As]2S[As]1S2 UKUVVAMSXXBMRX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- -1 molecular phosphorus compound Chemical class 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 230000004783 oxidative metabolism Effects 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
Landscapes
- Purification Treatments By Anaerobic Or Anaerobic And Aerobic Bacteria Or Animals (AREA)
- Treatment Of Sludge (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、家庭下水ないし、産業廃液、それに類する有
機性廃液などの有機物とリンを含む廃液の処理法に関す
るもので、特に嫌気−好気活性汚泥法と言われる生物脱
リン技術の改良に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for treating wastewater containing organic matter and phosphorus, such as domestic sewage, industrial wastewater, and similar organic wastewater. This is related to the improvement of dephosphorization technology.
一般に、嫌気−好気活性汚泥法とは、従来の活性汚泥法
施設における曝気槽の原液流入端を溶存酸素(DO)も
硝酸根あるいは亜硝酸根(NOx )も実質的に存在し
ない嫌気性状態の帯域c以下これを嫌気槽という)にし
、ここで被処理液と返送汚泥を混合し、しかるのちにこ
の混合液を後段の曝気された帯域(以下これを好気槽と
いう)に導いて曝気処理し、さらに沈殿池で固液分離を
はかる技術である。このような特徴のある嫌気−好気活
性汚泥法の工程構成では、標準活性汚泥法で生成される
活性汚泥よりもリン摂取能力の高い活性汚泥が生成され
、BOD 、 SSなどの汚濁物の除去と同時に原液中
に存在する溶解性リンの大部分を活性汚泥に吸収せしめ
ることができる。In general, the anaerobic-aerobic activated sludge method refers to the inflow end of the raw solution in the aeration tank in a conventional activated sludge method facility being kept in an anaerobic state in which dissolved oxygen (DO), nitrate radicals, or nitrite radicals (NOx) are substantially absent. The liquid to be treated and the returned sludge are mixed here, and the mixed liquid is then led to the aerated zone in the latter stage (hereinafter referred to as an aerobic tank) where it is aerated. This technology involves processing and then separating solid-liquid in a sedimentation tank. The process configuration of the anaerobic-aerobic activated sludge method, which has such characteristics, produces activated sludge that has a higher phosphorus uptake capacity than the activated sludge produced by the standard activated sludge method, making it easier to remove pollutants such as BOD and SS. At the same time, most of the soluble phosphorus present in the stock solution can be absorbed into the activated sludge.
このような嫌気−好気活性汚泥法で生成される活性汚泥
は、標準的な活性汚泥法で生成される汚泥よりもリン含
有率が高く、嫌気状態におかれた場合には汚泥中からリ
ンが再放出され、余剰汚泥の濃縮脱水工程で生ずる分離
液中に高濃度のリンが含有されることになる。したがっ
て、この分離液の処理も必要となり、該処理系の流入端
に返送され、被処理液とともに処理される。しかしなが
ら、この分離液を返送することは該処理系の流入リン負
荷量の増大を来たし、嫌気−好気活性汚泥法におけるリ
ン除去性能を低下させたり、不安定なものにするので問
題があった。The activated sludge produced by this anaerobic-aerobic activated sludge process has a higher phosphorus content than the sludge produced by the standard activated sludge process, and when placed in anaerobic conditions, phosphorus is removed from the sludge. is re-released, and the separated liquid produced in the process of concentrating and dewatering excess sludge contains a high concentration of phosphorus. Therefore, this separated liquid also needs to be treated, and is returned to the inflow end of the treatment system and treated together with the liquid to be treated. However, returning this separated liquid increases the amount of phosphorus that flows into the treatment system, which causes problems in that it reduces the phosphorus removal performance in the anaerobic-aerobic activated sludge process and makes it unstable. .
本発明は、これら従来の嫌気−好気活性汚泥法の欠点を
排除し、処理系のリン負荷量の増大を防止し、リン除去
を常に安定して行わしめる方法を提供することを目的と
するものである。The present invention aims to provide a method that eliminates these drawbacks of the conventional anaerobic-aerobic activated sludge method, prevents an increase in the amount of phosphorus loaded in the treatment system, and always performs stable phosphorus removal. It is something.
本発明は、嫌気−好気活性汚泥法で生成される余剰汚泥
を一旦濃縮分離し、濃縮分離した濃縮汚泥を2時間未満
の反応時間で曝気したのち脱水処理を行うことを特徴と
するものである。The present invention is characterized in that surplus sludge produced by an anaerobic-aerobic activated sludge method is once concentrated and separated, and the concentrated and separated thickened sludge is aerated in a reaction time of less than 2 hours, and then dehydrated. be.
本発明の一実施態様を図面に基づいて説明すると、家庭
下水などの有機性廃液である被処理液21は沈殿返送汚
泥22とともに嫌気槽1に導かれ攪拌機1′で混合され
て嫌気処理される。活性汚泥はここでその細胞内に貯留
した高分子リン化合物(ボIJ IJン酸)を加水分解
し溶液側に放出するとともにこの際に得られるエネルギ
ーを利用して、被処理液に含まれるBODの一部を細胞
内に摂取し、細胞内貯留有機物とする。この嫌気処理の
反応を行わしめる嫌気槽1の規模は被処理液21の組成
や濃度によって異なるが、家庭下水を被処理液とした場
合には、被処理液流入量の0.5〜2.5時間分でよい
。One embodiment of the present invention will be described based on the drawings. A liquid to be treated 21, which is an organic waste liquid such as domestic sewage, is led to an anaerobic tank 1 together with sedimentation return sludge 22, mixed by an agitator 1', and subjected to anaerobic treatment. . Activated sludge hydrolyzes the high molecular phosphorus compound (BOIJ phosphoric acid) stored in its cells and releases it into the solution, and uses the energy obtained at this time to remove BOD contained in the liquid to be treated. A part of it is taken into the cells and becomes intracellularly stored organic matter. The scale of the anaerobic tank 1 in which this anaerobic treatment reaction takes place varies depending on the composition and concentration of the liquid to be treated 21, but when domestic sewage is used as the liquid to be treated, it is 0.5 to 2. 5 hours is enough.
このようにして溶解性リンが増加し、BODが減少した
嫌気槽流出混合液23は、連設又は連通状態下に区画さ
れた好気槽2に導かれる。この好気槽2は空気その他の
酸素含有性気体を散気器2′から給気して曝気されてお
り、嫌気槽流出混合液23に含まれる活性汚泥は嫌気槽
1で摂取しきれなかったBOD成分を摂取し、酸化分解
するとともに細胞内貯留有機物も酸化分解される。また
、該活性汚泥は、この有機物の酸化代謝の際に生成され
るエネルギーの一部を利用して、細胞外に存在する溶解
性リンを細胞内に摂取しつつ細胞内に高分子リン化合物
(ボIJ IJン酸)を合成する。この際に嫌気槽1で
放出された以上の量の溶解性リンが摂取され、混合液中
の溶解性リン濃度は被処理液のそれよりも低くなるが、
完全な溶解性リン除去を行なうためには、被処理液のP
/BOD比が日間平均値で0.06以下であることが必
要であるが、家庭下水の多くはその条件を満たす。この
場合、BODの酸化分解と溶解性リン除去を完遂せしめ
るためには、好気槽2のBOD汚泥負荷F/M比を0.
05〜07(1/日)、好ましくは0.3〜o、5.(
t/日)の範囲に制御する必要がある。The anaerobic tank effluent mixed liquid 23 in which soluble phosphorus has increased and BOD has decreased in this way is led to the aerobic tank 2 which is partitioned in a continuous or communicating state. This aerobic tank 2 is aerated by supplying air or other oxygen-containing gas from an aeration diffuser 2', and the activated sludge contained in the anaerobic tank outflow mixed liquid 23 could not be completely absorbed by the anaerobic tank 1. BOD components are ingested and oxidized and decomposed, and the organic matter stored in the cells is also oxidized and decomposed. In addition, the activated sludge utilizes a part of the energy generated during the oxidative metabolism of organic matter to take in soluble phosphorus existing outside the cells, and to add polymeric phosphorus compounds ( Synthesize bo-IJ (IJ acid). At this time, soluble phosphorus in an amount greater than that released in the anaerobic tank 1 is ingested, and the soluble phosphorus concentration in the mixed liquid becomes lower than that in the liquid to be treated.
In order to completely remove soluble phosphorus, the P of the liquid to be treated must be
/BOD ratio is required to be 0.06 or less as a daily average value, and most domestic sewage satisfies this condition. In this case, in order to complete the oxidative decomposition of BOD and the removal of soluble phosphorus, the BOD sludge load F/M ratio of the aerobic tank 2 must be set to 0.
05-07 (1/day), preferably 0.3-o, 5. (
t/day).
かくして好気槽2で生成され、BODと溶解性リンが減
少した好気槽流出混合液24は沈殿池6に送られ、処理
液25と沈殿汚泥22に固液分離される。The aerobic tank effluent mixed liquid 24 generated in the aerobic tank 2 and reduced in BOD and soluble phosphorus is sent to the settling tank 6 and is separated into solid and liquid into a treated liquid 25 and settled sludge 22.
この沈殿汚泥22の一部は返送汚泥として嫌気槽1に返
送され、残部は余剰汚泥26として重力式濃縮槽4に移
送され、濃縮槽上澄液27と濃縮汚泥28に分離される
。A part of this settled sludge 22 is returned to the anaerobic tank 1 as return sludge, and the remainder is transferred to the gravity thickening tank 4 as excess sludge 26 and separated into thickening tank supernatant liquid 27 and thickened sludge 28.
従来、嫌気−好気活性汚泥法の汚泥を濃縮する場合、汚
泥からリンが放出されることから、濃縮槽上澄液27中
のリン濃度は濃縮汚泥28間隙水中のリン濃度と同等と
考えられており、余剰汚泥を濃縮せずに曝気して、放出
されたリンを汚泥に吸収させる方法をとっていた。しか
しこの方法においてけ、汚泥濃度も低く、大容量の汚泥
曝気槽が必要となり、その曝気槽に供給する空気量も汚
泥を均一に曝気するために多くなる。更に嫌気汚泥を曝
気することで硫化水素、アンモニア、酪酸等の悪臭物質
が飛散する。Conventionally, when sludge is concentrated using the anaerobic-aerobic activated sludge method, phosphorus is released from the sludge, so the phosphorus concentration in the thickening tank supernatant liquid 27 is considered to be equivalent to the phosphorus concentration in the thickened sludge 28 pore water. The method used was to aerate the excess sludge without concentrating it and absorb the released phosphorus into the sludge. However, in this method, the sludge concentration is low and a large-capacity sludge aeration tank is required, and the amount of air supplied to the aeration tank is also large in order to uniformly aerate the sludge. Furthermore, by aerating the anaerobic sludge, foul-smelling substances such as hydrogen sulfide, ammonia, and butyric acid are dispersed.
ところが、本発明の濃縮槽4における濃縮槽上澄液27
と濃縮汚泥28の間隙水中のリンの分布状況を調査した
ところ、第3図に示したような結果が得られた。すなわ
ち、濃縮槽上澄液27中に放出されたリン量は、汚泥の
保持しているリンの2〜3チにすぎなかった。したがっ
て、濃縮槽上澄液27を直接嫌気槽1に返送してもリン
の除去に及ぼす影響は殆んどない。However, the concentration tank supernatant liquid 27 in the concentration tank 4 of the present invention
When the distribution of phosphorus in the pore water of the thickened sludge 28 was investigated, the results shown in Figure 3 were obtained. That is, the amount of phosphorus released into the thickening tank supernatant liquid 27 was only 2 to 3 times the amount of phosphorus held in the sludge. Therefore, even if the concentration tank supernatant liquid 27 is directly returned to the anaerobic tank 1, there is almost no effect on the removal of phosphorus.
次に本発明では、濃縮槽4で分離された濃縮汚泥28は
汚泥曝気槽5に移送され、ここで2時間未満の曝気処理
をうける。Next, in the present invention, the thickened sludge 28 separated in the thickening tank 4 is transferred to the sludge aeration tank 5, where it is subjected to an aeration treatment for less than 2 hours.
ところで、濃縮汚泥28の間隙水中のリンが汚泥に吸収
される反応は次の(1)式に示すように、−次反応であ
り、汚泥濃度が高くなればリンが汚泥に吸収される時間
は大幅に短縮され、濃縮汚泥28の濃度が1,5%以上
であれば2時間未満で十分に濃縮汚泥28の間隙水中の
リンを汚泥に再吸収でき、汚泥曝気槽5は好気槽2の容
量の茄〜πですむ1、”? −−ku 5a−P (1
)
t
1化:汚泥のリン摂取速度係数(t/?hr>本発明の
場合 ku = 0.1〜1.O8a:濃縮汚泥濃度
Pニリン濃度
このように、汚泥濃度を高くして、汚泥曝気槽5の容量
を小さくできることは、建設費等の費用が節減されるだ
けでなく、汚泥を曝気することで飛散する排気ガス5“
中の硫化水素、アンモニア。By the way, the reaction in which phosphorus in the pore water of the thickened sludge 28 is absorbed into the sludge is a -order reaction, as shown in the following equation (1), and as the sludge concentration increases, the time for phosphorus to be absorbed into the sludge increases. If the concentration of the thickened sludge 28 is 1.5% or more, the phosphorus in the pore water of the thickened sludge 28 can be fully reabsorbed into the sludge in less than 2 hours, and the sludge aeration tank 5 Capacity is ~π 1,"? --ku 5a-P (1
) t 1 conversion: Phosphorus uptake rate coefficient of sludge (t/?hr > In the case of the present invention ku = 0.1 ~ 1. Being able to reduce the capacity of the tank 5 not only reduces costs such as construction costs, but also reduces the amount of exhaust gas 5" that is scattered by aerating the sludge.
Hydrogen sulfide and ammonia inside.
酪酸等を脱臭設備6で除去する上で好都合となる。This is convenient for removing butyric acid and the like with the deodorizing equipment 6.
したがって、悪臭物質の飛散をなるべく少なくするよう
に、汚泥曝気槽5への酸素含有気体5′の導入を汚泥曝
気槽5内の溶存酸素(Do)濃度で制御するとよい。す
なわち、汚泥のリン摂取反応はDOI〜υμで1−分で
あり、DO計8によりDO2W/j以上が検出されるよ
うな場合は弁8′により酸素含有気体5′の導入量を調
節すればよい。Therefore, it is preferable to control the introduction of the oxygen-containing gas 5' into the sludge aeration tank 5 by controlling the dissolved oxygen (Do) concentration in the sludge aeration tank 5 so as to reduce the scattering of malodorous substances as much as possible. That is, the phosphorus uptake reaction of sludge takes 1 minute at DOI~υμ, and if the DO meter 8 detects DO2W/j or more, the amount of oxygen-containing gas 5' introduced can be adjusted using the valve 8'. good.
とりわけ、本発明において酸素含有気体5′として酸素
含有率95チ以上の気体を用いると、排気ガス5“の量
が空気を用いる場合より更に少なくなり、悪臭物質も殆
んど曝気中に分解されるので、悪臭物質の除去の点で効
果的である。Particularly, in the present invention, when a gas with an oxygen content of 95 cm or more is used as the oxygen-containing gas 5', the amount of exhaust gas 5'' is even smaller than when air is used, and most of the malodorous substances are decomposed during aeration. Therefore, it is effective in removing malodorous substances.
このように、汚泥曝気槽5の酸素含有気体5′の童をな
るべく少なくしてDo濃度を1〜21JfAにするKは
汚泥曝気槽5を密閉型とし、表面曝気装置10で気液接
触させるほうが好ましい。In this way, in order to reduce the concentration of the oxygen-containing gas 5' in the sludge aeration tank 5 as much as possible to achieve a Do concentration of 1 to 21 JfA, it is better to make the sludge aeration tank 5 a closed type and bring the gas into liquid contact with the surface aeration device 10. preferable.
また汚泥曝気槽5内のpHを6〜9にすると、硫化水素
、アンモニア、酪酸等がガス体となる割合が少ないだけ
でなく、汚泥のリン吸収に最も適した雰囲気となる。し
たがって、汚泥曝気槽5内のpH計9により薬注ポンプ
9′のpH調節用薬品注入量を制御することが好ましい
。Further, when the pH in the sludge aeration tank 5 is set to 6 to 9, not only is the proportion of hydrogen sulfide, ammonia, butyric acid, etc. in gaseous form reduced, but the atmosphere is most suitable for sludge absorption of phosphorus. Therefore, it is preferable that the pH meter 9 in the sludge aeration tank 5 controls the amount of pH adjusting chemicals injected into the chemical injection pump 9'.
このように汚泥曝気槽5において、反応時間2時間未満
で曝気された曝気濃縮汚泥29は脱水機7に導入され脱
水処理される。脱水機7としてはベルトプレス脱水機、
遠心脱水機、真空脱水機等の通常の脱水機が使用され、
脱水汚泥は乾燥、焼却等で処分される。脱水機7からの
脱水ろ液30は嫌気槽1に返送され処理される。The aerated concentrated sludge 29 thus aerated in the sludge aeration tank 5 for a reaction time of less than 2 hours is introduced into the dehydrator 7 and dehydrated. The dehydrator 7 is a belt press dehydrator,
Regular dehydrators such as centrifugal dehydrators and vacuum dehydrators are used,
Dehydrated sludge is disposed of by drying, incineration, etc. The dehydrated filtrate 30 from the dehydrator 7 is returned to the anaerobic tank 1 for treatment.
第2図示例は、第1図示例と基本的には同様であるが、
嫌気槽1と好気槽2の間に脱窒紫檀11を設け、嫌気槽
1の流出混合液23と好気槽流出混合液24を脱窒紫檀
11に導入し、混合攪拌することにより、この混合g2
4に含まれるNOxが脱窒されるとともに、嫌気槽流出
混合液23に含まれる溶解性リンの一部が汚泥中に吸収
される。このため第2図の方法においては、原水中のB
OD、リン除去だけでなく、窒素除去も可能となる。The second illustrated example is basically the same as the first illustrated example, but
A denitrifying rosewood 11 is provided between the anaerobic tank 1 and the aerobic tank 2, and the effluent mixed liquid 23 of the anaerobic tank 1 and the aerobic tank effluent mixed liquid 24 are introduced into the denitrifying rosewood 11 and mixed and stirred. mixed g2
4 is denitrified, and a portion of the soluble phosphorus contained in the anaerobic tank outflow mixed liquid 23 is absorbed into the sludge. Therefore, in the method shown in Figure 2, B in the raw water is
Not only OD and phosphorus removal, but also nitrogen removal becomes possible.
以上のように、本発明においては、嫌気−好気活性汚泥
法の沈殿池からの余剰汚泥を濃縮分離し、この濃縮分離
した濃縮汚泥を2時間未満の反応時間で曝気したのち脱
水処理を行うことにより、少量の曝気用気体で濃縮槽上
澄液や脱水ろ液中のリン濃度を低下させ、これら汚泥処
理系からのリンの返送量を軽減し、嫌気−好気活性汚泥
法の処理系のリン負荷量の増大を防止し、リン除去を常
に安定化させることができる。As described above, in the present invention, excess sludge from the settling tank of the anaerobic-aerobic activated sludge method is concentrated and separated, and the concentrated and separated thickened sludge is aerated for a reaction time of less than 2 hours, and then dehydrated. This reduces the phosphorus concentration in the thickening tank supernatant liquid and dewatered filtrate with a small amount of aeration gas, reduces the amount of phosphorus returned from these sludge treatment systems, and improves the anaerobic-aerobic activated sludge treatment system. It is possible to prevent an increase in the amount of phosphorus loaded and to constantly stabilize phosphorus removal.
次に本発明の実施例を比較例と対照して示す。Next, examples of the present invention will be shown in comparison with comparative examples.
実施例−1
住宅団地より排出された家庭下水を被処理液として、第
1図示例の方法で処理した。それぞれの装置仕様は次の
通りであった。Example 1 Domestic sewage discharged from a residential complex was treated as the liquid to be treated by the method shown in the first illustrated example. The specifications of each device were as follows.
嫌 気 槽:2連式円筒攪拌槽 水容績 4n?好 気
槽:4画窒化矩形槽 〃 7ぜ沈 殿 池:円形クラ
リファイヤ 〃 7−重力式濃縮槽:円形クラリファイ
ヤ tt Q、5m’水面積 0.3m”
汚泥曝気4+1(4)円筒形攪拌器付曝気槽水容積 1
5を汚泥曝気槽(8)矩 形 楢 1/ 2501この
ような施設を用いて、被処理液量55−A、返送汚泥流
量15.4 m’/dで処理したところ、表−1に示す
ような処理液が得られた。Anaerobic tank: Double cylindrical stirring tank Water capacity 4n? Aerobic tank: 4-panel nitriding rectangular tank 〃 7-settlement pond: Circular clarifier 〃 7-Gravity thickening tank: Circular clarifier tt Q, 5m' water area 0.3m" Sludge aeration 4+1 (4) Cylindrical stirring Aeration tank water volume 1
5 was treated using a sludge aeration tank (8) rectangular oak 1/2501 using such a facility with a volume of treated liquid of 55-A and a return sludge flow rate of 15.4 m'/d, as shown in Table-1. A treatment solution like this was obtained.
表−1
この時の返送汚泥のMLSS濃度は1.2チ、好気槽の
MLSS濃度は2800ηβであった。Table 1 At this time, the MLSS concentration in the returned sludge was 1.2H, and the MLSS concentration in the aerobic tank was 2800ηβ.
また、返送汚泥の一部を重力式濃縮槽に導入した。この
重力式濃縮槽に導入した汚泥量は580t/dであった
。重力式濃縮槽からの引き抜き汚泥量を240 t/d
としたところ、重力式濃縮槽の汚泥界面は水面下100
0mでほぼ一定であり、濃縮汚泥濃度は2.9%であっ
た。この時の濃縮槽内の汚泥濃度分布およびリン濃度分
布は第3図に示した通りであった。In addition, a portion of the returned sludge was introduced into a gravity thickening tank. The amount of sludge introduced into this gravity thickening tank was 580 t/d. The amount of sludge drawn from the gravity thickening tank is 240 t/d.
As a result, the sludge interface in a gravity thickening tank is 100 m below the water surface.
It was almost constant at 0 m, and the thickened sludge concentration was 2.9%. The sludge concentration distribution and phosphorus concentration distribution in the thickening tank at this time were as shown in FIG.
さらに、この重力式濃縮槽の濃縮汚泥を汚泥曝気槽囚に
導入し、pH7に制御しDO1〜2 WIvtの条件下
で1.5時間空気で曝気した後遠心脱水を行った。Furthermore, the thickened sludge from this gravity thickening tank was introduced into a sludge aeration tank, the pH was controlled to 7, and the sludge was aerated with air for 1.5 hours under the conditions of DO1 to 2 WIvt, followed by centrifugal dehydration.
その結果は表−2の通りであり、この表からも分るよう
に、本発明の場合は重力式濃縮槽の上澄液と脱水ろ液中
の全リン量は2.11 r/dであり、必要空気量は0
.15 Ni/dであった。The results are shown in Table 2, and as can be seen from this table, in the case of the present invention, the total phosphorus content in the supernatant liquid and dehydrated filtrate of the gravity thickening tank was 2.11 r/d. Yes, the required air amount is 0
.. It was 15 Ni/d.
比較例−1
沈殿汚泥を汚泥貯留槽に導入し、10.3時間嫌気的に
貯留した後遠心脱水を行った。この結果は表=2に示し
た通りで、この場合の脱水ろ液中の全リン量は32.7
p/dであった。Comparative Example-1 Precipitated sludge was introduced into a sludge storage tank, stored anaerobically for 10.3 hours, and then centrifugally dehydrated. The results are shown in Table 2, and the total amount of phosphorus in the dehydrated filtrate in this case is 32.7
It was p/d.
比較例−2
沈殿汚泥を一旦250tの汚泥貯留槽に貯留した後、容
量250tの汚泥曝気槽(B)で10.3時間空気で曝
気した後遠心脱水を行った。Comparative Example 2 Precipitated sludge was once stored in a 250 t sludge storage tank, and then aerated with air for 10.3 hours in a 250 t capacity sludge aeration tank (B), followed by centrifugal dewatering.
この結果は表−2に示した通りで、この場合の脱水ろ液
中の全リン量は3.Or/dと少なかったが、必要空気
量は1.ONm’/dであった。The results are shown in Table 2, and the total amount of phosphorus in the dehydrated filtrate in this case was 3. Although it was small at Or/d, the required air amount was 1. ONm'/d.
これらの結果からも明らかなように、本発明によれば汚
泥曝気槽における空気供給量は著しく削減され、しかも
汚泥処理系における液中のリンの量は少なく、これを嫌
気槽に返送して処理してもリンの負荷量の増大を最小限
とし、安定した処理が行われた。As is clear from these results, according to the present invention, the amount of air supplied to the sludge aeration tank is significantly reduced, and the amount of phosphorus in the liquid in the sludge treatment system is small, which can be returned to the anaerobic tank for treatment. However, stable treatment was achieved with minimal increase in phosphorus loading.
実施例−2
実施例1における汚泥曝気槽で使用した空気に代えて酸
素含有率99チの純w1.素を用いた。この場合と、上
記実施例1及び比較例2において排ガスとして放出され
た悪臭物質量を、表−3に示した。Example 2 In place of the air used in the sludge aeration tank in Example 1, pure w1. The raw material was used. Table 3 shows the amounts of malodorous substances released as exhaust gas in this case, Example 1, and Comparative Example 2.
表−3に示したように本発明の場合は比較例−1
2にくらべて悪臭物質の排出量が荀に低減ルている。こ
れは、本発明の場合は排ガス量が少なく、悪臭物質の飛
散の点でも効果的であったことを示すものである。As shown in Table 3, in the case of the present invention, the amount of malodorous substances discharged was significantly reduced compared to Comparative Examples 1 and 2. This indicates that the present invention had a small amount of exhaust gas and was effective in scattering malodorous substances.
第1図は本発明の一実施態様を示す系統説明図、第2図
は本発明の他の実施態様を示す系統説明図で、第3図は
重力式濃縮槽内における水深と汚泥濃度及び全リン濃度
の分布を示す線図である。
1・・・嫌気槽、2・・・好気槽、6・・・沈殿池、4
・・・重力式濃縮槽、5・・・汚泥曝気槽、7・・・脱
水機、8・・・DO計、9・・・pH計、11・・・脱
窒素槽、21・・・被処理液、22・・・沈殿汚泥、2
3・・・嫌気槽流出混合液、24・・・好気槽流出混合
液、25・・・処理液、26・・・余剰汚泥、27・・
・濃縮槽上澄液、28・・・濃縮汚泥、汐・・・曝気濃
縮汚泥、30・・・脱水ろ液。Fig. 1 is a system explanatory diagram showing one embodiment of the present invention, Fig. 2 is a system explanatory diagram showing another embodiment of the present invention, and Fig. 3 shows water depth, sludge concentration, and total concentration in a gravity thickening tank. FIG. 2 is a diagram showing the distribution of phosphorus concentration. 1...Anaerobic tank, 2...Aerobic tank, 6...Sedimentation tank, 4
... Gravity thickening tank, 5... Sludge aeration tank, 7... Dehydrator, 8... DO meter, 9... pH meter, 11... Denitrification tank, 21... Cover Treatment liquid, 22...Settled sludge, 2
3...Anaerobic tank effluent mixed liquid, 24...Aerobic tank effluent mixed liquid, 25...Treatment liquid, 26...Excess sludge, 27...
- Thickening tank supernatant liquid, 28... Thickened sludge, Shio... Aerated thickened sludge, 30... Dehydrated filtrate.
Claims (1)
して嫌気処理したのち曝気処理を行い、該曝気混合液を
沈殿分離し、分離された沈殿汚泥の一部を前記返送汚泥
とし残部を濃縮分離し、分離された濃縮汚泥を酸素含有
気体で2時間未満曝気したのち脱水処理を行うことを特
徴とする有機性廃液の処理方法。 2 前記濃縮汚泥の濃度を少なくとも1.5%とするも
のである特許請求の範囲第1項記載の有機性廃液の処理
方法。 3 前記濃縮汚泥の曝気において、曝気汚泥中の溶存酸
素濃度を1〜2WAに制御するものである特許請求の範
囲第1項又は第2項記載の有機性廃液の処理方法。 4 前記濃縮汚泥の曝気において、酸素含有率95チ以
上の気体を用いるものである特許請求の範囲第1項、第
2項又は第3項記載の有機性廃液の一処理方法。 5 前記濃縮汚泥の曝気において、pHを6〜9に制御
するものである特許請求の範囲第1項、第2項、第3項
又は第4項記載の有機性廃液の処理方法。 6、 前記曝気混合液を返送し、前記嫌気処理混合液と
混合して脱窒未処理するものである特許請求の範囲第1
項、第2項、第3項、第4項又は第5項記載の有機性廃
液の処理方法。[Claims] 1. The rupture solution and return sludge are mixed with dissolved oxygen and nitric acid. Mix in an anaerobic state in which none of the nitrites are substantially present, perform anaerobic treatment, then perform aeration treatment, separate the aerated mixture by precipitation, and use a portion of the separated precipitated sludge as the return sludge and the remainder. A method for treating organic waste liquid, which comprises concentrating and separating the sludge, aerating the separated thickened sludge with an oxygen-containing gas for less than 2 hours, and then dehydrating the sludge. 2. The method for treating organic waste liquid according to claim 1, wherein the concentration of the thickened sludge is at least 1.5%. 3. The method for treating organic waste liquid according to claim 1 or 2, wherein in aeration of the thickened sludge, the dissolved oxygen concentration in the aerated sludge is controlled to 1 to 2 WA. 4. A method for treating organic waste liquid according to claim 1, 2 or 3, wherein a gas having an oxygen content of 95 cm or more is used in aeration of the thickened sludge. 5. The method for treating organic waste liquid according to claim 1, 2, 3, or 4, wherein the pH is controlled to 6 to 9 during aeration of the thickened sludge. 6. Claim 1, wherein the aerated mixture is returned and mixed with the anaerobic treatment mixture to undergo denitrification treatment.
The method for treating organic waste liquid according to item 1, item 2, item 3, item 4, or item 5.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58149620A JPS6041594A (en) | 1983-08-18 | 1983-08-18 | Treatment of organic waste liquid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58149620A JPS6041594A (en) | 1983-08-18 | 1983-08-18 | Treatment of organic waste liquid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6041594A true JPS6041594A (en) | 1985-03-05 |
| JPS6356838B2 JPS6356838B2 (en) | 1988-11-09 |
Family
ID=15479193
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58149620A Granted JPS6041594A (en) | 1983-08-18 | 1983-08-18 | Treatment of organic waste liquid |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6041594A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0283100A (en) * | 1988-09-19 | 1990-03-23 | Japan Organo Co Ltd | Water purifying treatment plant |
| NL1025346C2 (en) * | 2004-01-29 | 2005-08-01 | Seghers Keppel Technology Grou | A method for treating organic sludge. |
| WO2008046139A1 (en) * | 2006-10-16 | 2008-04-24 | Environmental Biotechnology Crc Pty Limited | Wastewater treatment |
-
1983
- 1983-08-18 JP JP58149620A patent/JPS6041594A/en active Granted
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0283100A (en) * | 1988-09-19 | 1990-03-23 | Japan Organo Co Ltd | Water purifying treatment plant |
| NL1025346C2 (en) * | 2004-01-29 | 2005-08-01 | Seghers Keppel Technology Grou | A method for treating organic sludge. |
| EP1559688A1 (en) * | 2004-01-29 | 2005-08-03 | Seghers Keppel Technology Group | A method for the degradation of organic sludge |
| WO2008046139A1 (en) * | 2006-10-16 | 2008-04-24 | Environmental Biotechnology Crc Pty Limited | Wastewater treatment |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6356838B2 (en) | 1988-11-09 |
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