JPS6154445B2 - - Google Patents
Info
- Publication number
- JPS6154445B2 JPS6154445B2 JP6526382A JP6526382A JPS6154445B2 JP S6154445 B2 JPS6154445 B2 JP S6154445B2 JP 6526382 A JP6526382 A JP 6526382A JP 6526382 A JP6526382 A JP 6526382A JP S6154445 B2 JPS6154445 B2 JP S6154445B2
- Authority
- JP
- Japan
- Prior art keywords
- sludge
- concentration
- thickened
- carbon dioxide
- tank
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000010802 sludge Substances 0.000 claims description 198
- 230000008719 thickening Effects 0.000 claims description 29
- 238000005273 aeration Methods 0.000 claims description 24
- 238000004062 sedimentation Methods 0.000 claims description 8
- 239000013049 sediment Substances 0.000 claims description 3
- 239000012141 concentrate Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000002351 wastewater Substances 0.000 claims 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 68
- 229910002092 carbon dioxide Inorganic materials 0.000 description 34
- 239000001569 carbon dioxide Substances 0.000 description 34
- 239000007789 gas Substances 0.000 description 32
- 239000007788 liquid Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000010586 diagram Methods 0.000 description 5
- 239000010865 sewage Substances 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 230000001079 digestive effect Effects 0.000 description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
- 239000005416 organic matter Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 101100532097 Vitis rotundifolia RUN1 gene Proteins 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Description
本発明は、廃水処理プラントにおける濃縮槽の
汚泥浮上を防止し、濃縮汚泥濃度を向上させるよ
うにした濃縮槽の排泥制御装置に関する。
沈降性の良好な汚泥は濃縮槽に出来るだけ長時
間滞留させて濃縮汚泥濃度を向上させることが望
ましい。一方、沈降性が悪い汚泥の場合には、濃
縮槽内の汚泥が浮上するので出来るだけ早く汚泥
を引き抜く必要がある。
従来、濃縮槽の汚泥引き抜きは、濃縮汚泥濃度
あるいは汚泥界面を検出して、濃縮汚泥引き抜き
量を操作している。しかし、汚泥の沈降性を判定
することができないため、汚泥沈降性の変動に対
処することができなかつた。すなわち、汚泥が浮
上する場合には適用できず、また沈降性が良い場
合にも汚泥がいつ再浮上するか予測できないため
濃縮汚泥濃度がさらに増加する場合であつても途
中で引き抜かざるを得なかつた。
第1図は濃縮槽における汚泥滞留時間tと濃縮
汚泥濃度Cとの関係の一例を示す。第1図の特性
(a)は汚泥沈降性が比較的良好な汚泥(浮上しにく
い汚泥)の例を示し、特性(b)は汚泥沈降性が悪い
汚泥(浮上し易い汚泥)の例を示す。いずれの場
合でも、ある汚泥滞留時間(t1及びt2で示す。)ま
では濃縮汚泥濃度Cは増加する。しかし、滞留時
間が長くなるのに伴つて、濃縮汚泥濃度Cは低下
する。これは、汚泥が長時間蓄積すると浮上し易
くなる性質に起因している。沈降性の良い汚泥に
ついては汚泥滞留時間Tをt2とすることが出来れ
ば、(a)で示すように、濃縮汚泥濃度CはC2の濃
度が得られる。一方沈降性の悪い汚泥について
は、汚泥滞留時間をt1とすることが出来れば、濃
度C1が得られる。
ところが、汚泥の沈降性は処理場によつて異な
るだけでなく、時間的に大きく変動する。にもか
かわらず、従来法ではこの汚泥沈降性を予測でき
ない。
このため、濃縮汚泥濃度Cが一定になるように
濃縮汚泥を引き抜く方法では目標濃度をC1より
低い値に設定せざるを得ない。もし目標濃度を
C1より大きくとると、沈降性の悪い汚泥(b)に対
しては、C1より高い濃度になることはないから
濃縮汚泥はいつまでも引き抜かれず、汚泥が濃縮
槽内に蓄積して分離液中に溢流することになる。
そこで目標濃度をC1に設定すると、今度は沈降
性の良い汚泥(a)の場合には汚泥滞留時間をt2に選
べば濃縮汚泥濃度CがC2に増加するにもかかわ
らず途中で汚泥を引き抜くことになり、濃縮汚泥
濃度は増加しない。
汚泥界面を一定に制御する方法では、沈降性の
良い汚泥に対しては汚泥界面を計測できるが、沈
降性が悪く浮上し易い汚泥に対しては汚泥界面が
形成されないから汚泥界面計は使用できない。ま
た、汚泥界面だけを検出しても、汚泥が浮上を開
始して汚泥界面が形成されなくなつて初めて汚泥
界面計が使用できなくなつたことが判ることにな
り、このような沈降性の悪い汚泥には適用できな
い。沈降性が良い汚泥に対しても、汚泥沈降性が
いつ悪化するか不明であるから汚泥界面の設定値
は低く選ばざるを得ず、この結果、濃縮汚泥濃度
も低い値になる。
このように、従来の方法では結果的に濃縮汚泥
濃度が比較的低い状態の濃縮汚泥しか得られなか
つた。
このため、嫌気性消化槽の加温エネルギーが増
大したり、あるいは、脱水機用の薬品量が増大す
ることになる。また、汚泥が浮上した場合には汚
水処理プロセスに与える有機物負荷量、窒素及び
リン負荷量が増大し、汚水処理機能及び処理費を
増大させることになる。
本発明の目的は汚泥沈降性に応じて濃縮引き抜
き量を操作することにより濃縮槽内における汚泥
浮上を防止し濃縮汚泥濃度を向上させることので
きる濃縮槽の排泥制御装置を提供することにあ
る。
本発明の特徴は濃縮槽に流入する汚泥の沈降性
を曝気排ガス中特定成分(炭酸ガス、メタンガス
及び硫化水素ガス等)のガス濃度で判定し、この
ガス濃度を指標として、濃縮槽の汚泥滞留時間、
すなわち濃縮汚泥引き抜き量を制御することにあ
る。
まず、本発明の基本的考え方について説明す
る。
汚泥沈降性悪化の原因の一つとして汚泥の嫌気
性消化(とくに酸発酵)がある。つまり、最初沈
殿池に沈殿した汚泥は嫌気性状態になると沈殿中
の有機物が嫌気性消化菌の作用により分解され炭
酸ガスと有機酸等を生成する。炭酸ガスはほとん
どの量が液中に溶存するが、一部か微小気泡とな
つて汚泥フロツクに付着する。このため汚泥フロ
ツクの見掛上の密度が低下して沈降性が悪化し、
ガス付着量がさらに増加すると汚泥は浮上する。
従つて、汚泥中の炭酸ガス濃度が高ければ高い程
汚泥沈降性は悪くなる。
第2図は汚泥の回分沈降試験を行つたときの汚
泥中の炭酸ガス濃度が汚泥浮上時間(汚泥が液面
に浮上するまでの時間)に及ぼす影響を実験的に
求めた図である。第2図から汚泥中炭酸ガス濃度
が少ない程汚泥浮上時間が長いことがわかる。す
なわち、汚泥中炭酸ガス濃度は汚泥沈降性(又は
浮上性)の一つの指標と考えることができる。
嫌気性消化菌の作用によつて生成するガスとし
ては炭酸ガスの他に、メタンガス、硫化水素ガ
ス、水素ガス及びアンモニアガス等がある。ま
た、嫌気性状態では脱窒菌の作用によつて窒素ガ
ス、亜酸化窒素ガス等も微量だけ生成する。従つ
て、これらのガス濃度も汚泥沈降性の一指標と考
えられる。ガス濃度の検出精度から考えると、量
的に多い炭酸ガスが最も感度が高く好適である。
汚泥中の炭酸ガス濃度はオンラインで直接的に
測定するのは難しいが、汚泥を曝気して排出され
る曝気排ガス中の炭酸ガス濃度から計算すること
ができる。
汚泥中の炭酸ガス濃度と排ガス中炭酸ガス濃度
とは次の関係がある。
Cl=a・Qg・Cg ………(1)
ここで、Cl:汚泥中炭酸ガス濃度、Cg:排ガ
ス中炭酸ガス濃度、Qg:曝気風量、a:定数で
ある。曝気風量が一定の条件では、次式が成立す
る。
Cl=a′・Cg ………(2)
ここで、a′:aQgである。従つて、a′を事前に
求めておけば、排ガス中炭酸ガス濃度Cgを検出
することにより、汚泥中炭酸ガス濃度Clを推定
できる。曝気風量Qgが変る場合には、排ガス中
炭酸ガス濃度Cgの他に曝気風量Qgを検出して、
(1)式から汚泥中炭酸ガス濃度Clを計算できる。
汚泥中炭酸ガス濃度Clが高い場合には、汚泥
沈降性は悪く短時間で浮上する。この場合には濃
縮槽内に汚泥が長時間滞留しないように濃縮汚泥
を引き抜くことが必要である。逆に、汚泥中炭酸
ガス濃度Clが低い場合には、汚泥沈降性は良好
であり長時間浮上しない。汚泥は時間とともに濃
縮されて濃縮汚泥濃度は増加する。従つて、出来
るだけ長時間汚泥が濃縮槽内に滞留するように濃
縮汚泥引き抜き量を操作すれば、高精度の濃縮汚
泥が得られる。
第1図に示すように汚泥沈降性が(a)及び(b)のよ
うに変動しても汚泥沈降性に応じて濃縮汚泥引き
抜き量を操作するので、特性(a)の場合には濃縮汚
泥濃度はC1に近くでき、一方特性(b)の場合には
C2に近くでき、高濃度汚泥が得られる。
例えば、汚泥中炭酸ガス濃度Clが100ml/と
すると、第2図から汚泥浮上時間は約50時間とな
る。従つて、安全側に考えて40時間程度汚泥が濃
縮槽に滞留するように、濃縮汚泥引き抜き量を操
作すれば、汚泥浮上を防止し、かつ高濃度の濃縮
汚泥を得ることができる。
発明者らは657の濃縮槽と9.1の汚泥曝気槽
を有する実験装置を用い、下水処理場の濃縮槽に
流入する汚泥を使用して実験した。実験条件及び
結果を下表に示す。
The present invention relates to a sludge discharge control device for a thickening tank in a wastewater treatment plant, which prevents sludge from floating in the thickening tank and improves the concentration of thickened sludge. It is desirable that sludge with good sedimentation properties be retained in a thickening tank for as long as possible to improve the thickened sludge concentration. On the other hand, in the case of sludge with poor settling properties, the sludge in the thickening tank floats to the surface, so it is necessary to pull out the sludge as quickly as possible. Conventionally, when extracting sludge from a thickening tank, the concentrated sludge concentration or the sludge interface is detected to control the amount of thickened sludge extracted. However, since it is not possible to determine the settling property of sludge, it has not been possible to deal with fluctuations in sludge settling property. In other words, it cannot be applied when sludge floats to the surface, and even when the sludge has good settling properties, it is impossible to predict when the sludge will resurface, so even if the concentration of thickened sludge increases further, it is necessary to remove it midway through the process. Ta. FIG. 1 shows an example of the relationship between the sludge residence time t and the thickened sludge concentration C in the thickening tank. Characteristics in Figure 1
Characteristic (a) shows an example of sludge with relatively good sludge settling properties (sludge that does not easily float to the surface), and characteristic (b) shows an example of sludge that has poor sludge settling properties (sludge that easily floats to the surface). In either case, the thickened sludge concentration C increases until a certain sludge retention time (indicated by t1 and t2 ). However, as the residence time becomes longer, the concentrated sludge concentration C decreases. This is due to the fact that sludge tends to float when it accumulates for a long time. For sludge with good settling properties, if the sludge residence time T can be set to t2 , the concentrated sludge concentration C will be C2 , as shown in (a). On the other hand, for sludge with poor settling properties, if the sludge residence time can be set to t 1 , a concentration C 1 can be obtained. However, the settling ability of sludge not only differs depending on the treatment plant, but also varies greatly over time. However, conventional methods cannot predict this sludge settling property. For this reason, in the method of drawing out thickened sludge so that the thickened sludge concentration C becomes constant, the target concentration must be set to a value lower than C1 . If the target concentration
If the concentration is higher than C 1 , the concentration of sludge (b) with poor settling properties will never be higher than C 1 , so the thickened sludge will not be drawn out forever, and the sludge will accumulate in the thickening tank and become trapped in the separated liquid. It will overflow.
Therefore, if the target concentration is set to C 1 , then in the case of sludge (a) with good settling properties, if the sludge retention time is chosen to be t 2 , the sludge will drop midway even though the thickened sludge concentration C increases to C 2 . The thickened sludge concentration will not increase. With the method of controlling the sludge interface at a constant level, the sludge interface can be measured for sludge that has good settling properties, but the sludge interface meter cannot be used for sludge that has poor settling properties and easily floats because the sludge interface is not formed. . Furthermore, even if only the sludge interface is detected, it is only when the sludge starts to float and the sludge interface is no longer formed that the sludge interface meter becomes unusable. Not applicable to sludge. Even for sludge with good settling properties, it is unclear when the sludge settling properties will deteriorate, so the set value of the sludge interface must be selected low, and as a result, the concentrated sludge concentration also becomes a low value. As described above, in the conventional method, only thickened sludge with a relatively low concentration of thickened sludge could be obtained. Therefore, the heating energy for the anaerobic digestion tank increases, or the amount of chemicals for the dehydrator increases. Moreover, when sludge floats to the surface, the amount of organic matter load, nitrogen and phosphorus load applied to the sewage treatment process increases, which increases the sewage treatment function and treatment cost. An object of the present invention is to provide a sludge drainage control device for a thickening tank that can prevent sludge from floating in the thickening tank and improve the concentration of thickened sludge by controlling the amount of thickened sludge drawn out according to the settling property of the sludge. . The feature of the present invention is that the sedimentation property of the sludge flowing into the thickening tank is determined by the gas concentration of specific components (carbon dioxide gas, methane gas, hydrogen sulfide gas, etc.) in the aeration exhaust gas, and this gas concentration is used as an index to determine the settling properties of the sludge in the thickening tank. time,
That is, the objective is to control the amount of thickened sludge drawn out. First, the basic idea of the present invention will be explained. Anaerobic digestion of sludge (especially acid fermentation) is one of the causes of worsening sludge settling properties. In other words, when the sludge that initially settles in the settling tank becomes anaerobic, the organic matter in the sediment is decomposed by the action of anaerobic digestive bacteria, producing carbon dioxide gas, organic acids, and the like. Most of the carbon dioxide gas is dissolved in the liquid, but some of it forms microbubbles and adheres to the sludge flocs. As a result, the apparent density of the sludge flocs decreases, resulting in poor settling properties.
If the amount of gas adhesion increases further, the sludge will float to the surface.
Therefore, the higher the carbon dioxide concentration in the sludge, the worse the sludge settling property becomes. FIG. 2 is a diagram obtained experimentally to determine the effect of carbon dioxide concentration in sludge on sludge floating time (time until sludge rises to the surface of the liquid) when performing a sludge batch sedimentation test. It can be seen from Figure 2 that the lower the carbon dioxide concentration in the sludge, the longer the sludge floating time. That is, the carbon dioxide concentration in sludge can be considered as one index of sludge settling (or flotation). Gases produced by the action of anaerobic digestive bacteria include, in addition to carbon dioxide gas, methane gas, hydrogen sulfide gas, hydrogen gas, and ammonia gas. In addition, in an anaerobic state, only trace amounts of nitrogen gas, nitrous oxide gas, etc. are produced by the action of denitrifying bacteria. Therefore, the concentration of these gases can also be considered as an indicator of sludge settling properties. Considering the detection accuracy of gas concentration, carbon dioxide gas, which is large in quantity, has the highest sensitivity and is suitable. Although it is difficult to directly measure the carbon dioxide concentration in sludge online, it can be calculated from the carbon dioxide concentration in the aeration exhaust gas discharged by aerating the sludge. The following relationship exists between the carbon dioxide concentration in sludge and the carbon dioxide concentration in exhaust gas. Cl=a・Qg・Cg (1) where Cl: carbon dioxide concentration in sludge, Cg: carbon dioxide concentration in exhaust gas, Qg: aeration air volume, and a: constant. Under conditions where the aeration air volume is constant, the following equation holds true. Cl=a′・Cg……(2) Here, a′: aQg. Therefore, if a' is determined in advance, the carbon dioxide concentration Cl in the sludge can be estimated by detecting the carbon dioxide concentration Cg in the exhaust gas. When the aeration air volume Qg changes, the aeration air volume Qg is detected in addition to the carbon dioxide concentration Cg in the exhaust gas.
The carbon dioxide concentration Cl in sludge can be calculated from equation (1). When the carbon dioxide concentration Cl in the sludge is high, the sludge has poor settling properties and floats to the surface in a short time. In this case, it is necessary to draw out the thickened sludge so that it does not remain in the thickening tank for a long time. Conversely, when the carbon dioxide concentration Cl in the sludge is low, the sludge has good settling properties and does not float for a long time. Sludge becomes thickened over time and the concentration of thickened sludge increases. Therefore, highly accurate thickened sludge can be obtained by controlling the amount of drawn-out thickened sludge so that the sludge stays in the thickening tank for as long as possible. As shown in Figure 1, even if the sludge settling property changes as shown in (a) and (b), the amount of thickened sludge withdrawn is controlled according to the sludge settling property, so in the case of characteristic (a), the thickened sludge The concentration can be close to C 1 , while for property (b)
It can be produced close to C 2 and high concentration sludge can be obtained. For example, if the carbon dioxide concentration Cl in the sludge is 100ml/, the sludge floating time will be approximately 50 hours as shown in Figure 2. Therefore, if the amount of thickened sludge to be drawn is controlled so that the sludge remains in the thickening tank for about 40 hours on the safe side, sludge floating can be prevented and highly concentrated thickened sludge can be obtained. The inventors used an experimental apparatus having 657 thickening tanks and 9.1 sludge aeration tanks, and conducted experiments using sludge flowing into the thickening tank of a sewage treatment plant. The experimental conditions and results are shown in the table below.
【表】
表より明らかなように、曝気処理の制御だけ
(RUN2)でも、曝気なしの従来法(RUN1)に対
して有効であるが、本発明による濃縮汚泥抜き出
し量を操作することにより、さらに濃縮汚泥濃度
を向上できることが確認された。
以下、本発明の一実施例を第3図により説明す
る。
流入下水は最初沈殿池1、エアレーシヨンタン
ク2を経て処理される。一方、最初沈殿池1内の
汚泥は汚泥ポンプ3により排出され、汚泥輸送管
4により汚泥曝気槽5に供給される。汚泥曝気槽
5には曝気用ブロワー6、ガス管7及び散気装置
8によりガスを供給され、汚泥が曝気される。曝
気後、汚泥は濃縮槽9へ供給され、沈降濃縮され
る。濃縮汚泥は濃縮汚泥ポンプ10により引き抜
かれる。曝気排ガスは炭酸ガス濃度計11により
ガス濃度が計測される。炭酸ガス濃度計として
は、赤外式、プロセスガスクロ式、膜電極式及び
半導体式等があるが、赤外式炭酸ガス分析計が好
適である。炭酸ガス濃度計11の計測値信号Cg
はガス濃度演算装置12に導かれ(2)式に基づき汚
泥中炭酸ガス濃度Clが演算される。汚泥ポンプ
3による汚泥輸送が連続的な場合には(2)式をその
まま適用できる。一方、間欠的な場合には、排ガ
ス中炭酸ガス濃度Cgは時間的に変動するので、
一定時間内の平均値Cgを用いれば良い。計算式
は例えば次式で表される。
=1/te−ts∫te tsCg(t)dt ………(3)
ここで、ts:平均値を計算する開始時間、t
e:平均値の計算する終了時間である。この場
合、汚泥中炭酸ガス濃度Clは次式で計算する。
Cl=a′ ………(4)
演算値Clは排出制御装置13において、濃縮
汚泥ポンプ10を作動させる信号に変換される。
この変換方法は例えば第4図の通りである。Cl
の演算値信号bは変換器101において、第1図
の関係を用いて汚泥浮上時間Tに変換されて信号
cになる。信号cを受けて、演算装置102にお
いて濃縮汚泥引き抜き量Qputが演算される。演
算式は次式である。
Qput=k/c ………(5)
ここで、kは定数であり、オペレーターが設定
できる。(3)式は信号c(汚泥浮止時間T)が大き
い程、つまり汚泥滞留時間が長い程、濃縮汚泥引
き抜き量Qputは小さくなることを意味する。Qpu
tは信号dとなつてタイマー回路103は起動信
号を送る。タイマー回路103は起動信号dを受
けてから所定時間だけ駆動信号eを駆動回路10
4に送る。駆動回路104は所定時間だけ濃縮汚
泥ポンプ10を作動させる。この作動時間はQpu
tが大きい程長くなる。
このようにして、汚泥中炭酸ガス濃度Clに応
じて、濃縮汚泥引き抜き量を操作する。
このようにして濃縮槽7からの汚泥引き抜き量
を制御するのであるが、浮上する時間まで許容し
得る時間だけ濃縮させているので、分離液に汚泥
を含ませることなく濃縮汚泥濃度を高くすること
ができる。
第5図は曝気風量Qgが変る場合の実施例を第
5図に示す。この場合、ガス流量計20で曝気風
量Qgを検出し、排ガス中炭酸ガス濃度Cgを用い
て汚泥中炭酸ガス濃度Clをガス濃度演算装置1
2において(1)式に基づき演算する。以下の制御は
第3図の実施例と同様である。第5図の実施例で
は曝気風量を操作する場合にも対応でき制御精度
が高いという利点がある。
次に、濃縮前に汚泥が曝気されるので、汚泥浮
上時間Tが長くなる。このため、濃縮汚泥引き抜
き量Qputは小さくなつて、汚泥が濃縮槽内に蓄
積して汚泥界面が上昇し過ぎる場合がある。汚泥
界面が上昇し過ぎると汚泥が分離液中に混入する
恐れがある。これを防止する実施例を第6図に示
す。
第6図に示す実施例は、第3図に示した実施例
に、さらに汚泥界面計21を付加して構成され
る。ここで22は汚泥界面検出端である。汚泥界
面計21により濃縮槽9の汚泥界面を検出し、検
出信号hが排出制御装置13′に送信される。制
御装置13′の処理フローを第7図に示す。界面
信号hは比較回路105に送られる。比較回路1
05には設定器106により汚泥界面の上限値h0
が与えられている。比較回路105はhh0のと
きタイマー回路107に起動信号iを与えると共
に駆動回路104に停止信号lを与え停止させ
る。一方、起動信号iによりタイマー回路107
が起動し一定時間だけ駆動信号jを駆動回路10
8に送る。駆動回路108は所定時間だけ濃縮汚
泥ポンプ10を作動させて濃縮汚泥を引き抜き汚
泥界面を低下させる。
このように、汚泥界面hが設定値h0より大きい
時には、第2図に示した実施例による濃縮汚泥引
き抜き操作に優先して、汚泥界面を低下させるよ
うに濃縮汚泥ポンプ10を作動させる。その結
果、濃縮槽内から汚泥が分離液中に混入するのを
防止できる。ここで、汚泥界面の上限設定値h0は
水面下1.0m前後が望ましい。
本発明によれば、汚泥の沈降性を検出して、こ
の沈降性に応じて濃縮槽から適量だけ濃縮汚泥が
引き抜かれる。つまり、沈降性が悪く浮上し易い
汚泥に対しては、濃縮槽に汚泥が長時間滞留しな
いように濃縮汚泥ポンプを操作し、汚泥が分離液
中に混入するのを防止する。この際には、濃縮槽
内の汚泥は浮上しない程度の適度の時間まで滞留
しているから、濃縮汚泥濃度も最高濃度に近くな
る。一方、沈降性を良好な汚泥に対しては出来る
だけ長時間汚泥が濃縮槽内に滞留するように濃縮
汚泥ポンプを操作するので、濃縮汚泥濃度は高く
なる。
このように、本発明では汚泥沈降性に応じて濃
度汚泥引き抜き量を操作するので、濃縮槽内での
汚泥浮上を防止できるとともに、濃縮汚泥濃度を
高く維持することができる。この結果、汚水処理
機能の低下を防止するとともに、汚泥処理コスト
の大幅な低減が可能となる。[Table] As is clear from the table, controlling the aeration process alone (RUN2) is effective against the conventional method without aeration (RUN1), but by manipulating the amount of thickened sludge extracted according to the present invention, it is even more effective. It was confirmed that the concentration of thickened sludge could be improved. An embodiment of the present invention will be described below with reference to FIG. The inflowing sewage first passes through a sedimentation tank 1 and an aeration tank 2 before being treated. On the other hand, the sludge in the initial settling tank 1 is discharged by the sludge pump 3 and supplied to the sludge aeration tank 5 through the sludge transport pipe 4. Gas is supplied to the sludge aeration tank 5 by an aeration blower 6, a gas pipe 7, and an aeration device 8, and the sludge is aerated. After aeration, the sludge is supplied to the thickening tank 9, where it is sedimented and concentrated. The thickened sludge is drawn out by the thickened sludge pump 10. The gas concentration of the aeration exhaust gas is measured by a carbon dioxide concentration meter 11. Examples of the carbon dioxide concentration meter include an infrared type, a process gas chromatography type, a membrane electrode type, and a semiconductor type, but an infrared type carbon dioxide gas analyzer is preferable. Measurement value signal Cg of carbon dioxide concentration meter 11
is guided to the gas concentration calculation device 12, and the carbon dioxide concentration Cl in the sludge is calculated based on equation (2). If sludge transport by the sludge pump 3 is continuous, equation (2) can be applied as is. On the other hand, in the intermittent case, the carbon dioxide concentration Cg in the exhaust gas fluctuates over time, so
It is sufficient to use the average value Cg within a certain period of time. The calculation formula is expressed, for example, by the following formula. =1/t e −t s ∫ te ts Cg(t) dt ………(3) Here, t s : start time for calculating the average value, t
e : End time for calculating the average value. In this case, the carbon dioxide concentration Cl in the sludge is calculated using the following formula. Cl=a' (4) The calculated value Cl is converted into a signal for operating the thickened sludge pump 10 in the discharge control device 13.
This conversion method is shown in FIG. 4, for example. Cl
The calculated value signal b is converted into the sludge floating time T by the converter 101 using the relationship shown in FIG. 1, and becomes the signal c. In response to the signal c, the arithmetic unit 102 calculates the amount of concentrated sludge pulled out Qput . The calculation formula is as follows. Q put =k/c (5) Here, k is a constant and can be set by the operator. Equation (3) means that the larger the signal c (sludge floating time T), that is, the longer the sludge retention time, the smaller the concentrated sludge withdrawal amount Qput . Q pu
t becomes a signal d, and the timer circuit 103 sends a start signal. The timer circuit 103 sends the drive signal e to the drive circuit 10 for a predetermined period of time after receiving the activation signal d.
Send to 4. The drive circuit 104 operates the thickened sludge pump 10 for a predetermined period of time. This operating time is Q pu
The larger t is, the longer it becomes. In this way, the amount of concentrated sludge drawn out is controlled according to the carbon dioxide concentration Cl in the sludge. In this way, the amount of sludge drawn out from the thickening tank 7 is controlled, and since the sludge is concentrated for an allowable time until it floats, it is possible to increase the concentrated sludge concentration without including sludge in the separated liquid. I can do it. FIG. 5 shows an example in which the aeration air volume Qg changes. In this case, the gas flow meter 20 detects the aeration air volume Qg, and the gas concentration calculation device 1 calculates the carbon dioxide concentration Cl in the sludge using the carbon dioxide concentration Cg in the exhaust gas.
In step 2, calculation is performed based on equation (1). The following control is similar to the embodiment shown in FIG. The embodiment shown in FIG. 5 has the advantage of being able to handle the case where the aeration air volume is controlled and having high control accuracy. Next, since the sludge is aerated before concentration, the sludge floating time T becomes longer. For this reason, the amount of thickened sludge pulled out Qput becomes small, and sludge may accumulate in the thickening tank, causing the sludge interface to rise too much. If the sludge interface rises too much, there is a risk that sludge will be mixed into the separated liquid. An embodiment for preventing this is shown in FIG. The embodiment shown in FIG. 6 is constructed by adding a sludge interface meter 21 to the embodiment shown in FIG. Here, 22 is a sludge interface detection end. The sludge interface in the thickening tank 9 is detected by the sludge interface meter 21, and a detection signal h is transmitted to the discharge control device 13'. FIG. 7 shows the processing flow of the control device 13'. The interface signal h is sent to the comparison circuit 105. Comparison circuit 1
In 05, the upper limit value h 0 of the sludge interface is set by the setting device 106.
is given. When hh0 , the comparator circuit 105 provides a start signal i to the timer circuit 107 and a stop signal l to the drive circuit 104 to stop it. On the other hand, the timer circuit 107
starts and sends the drive signal j for a certain period of time to the drive circuit 10.
Send to 8. The drive circuit 108 operates the thickened sludge pump 10 for a predetermined period of time to draw out the thickened sludge and lower the sludge interface. In this manner, when the sludge interface h is larger than the set value h 0 , the thickened sludge pump 10 is operated to lower the sludge interface in priority to the thickened sludge drawing operation according to the embodiment shown in FIG. As a result, it is possible to prevent sludge from being mixed into the separated liquid from within the thickening tank. Here, the upper limit setting value h 0 of the sludge interface is preferably about 1.0 m below the water surface. According to the present invention, the sedimentation property of sludge is detected, and an appropriate amount of thickened sludge is extracted from the thickening tank according to the sedimentation property. That is, for sludge that has poor settling properties and tends to float, the thickened sludge pump is operated so that the sludge does not remain in the thickening tank for a long time, thereby preventing the sludge from being mixed into the separated liquid. At this time, since the sludge in the thickening tank remains for an appropriate amount of time without floating, the thickened sludge concentration also approaches the maximum concentration. On the other hand, for sludge with good settling properties, the thickened sludge pump is operated so that the sludge stays in the thickening tank for as long as possible, so the thickened sludge concentration becomes high. In this way, in the present invention, the amount of concentrated sludge drawn out is controlled according to the sludge settling property, so that sludge floating in the thickening tank can be prevented and the concentrated sludge concentration can be maintained at a high level. As a result, it is possible to prevent a decline in the sewage treatment function and to significantly reduce the sludge treatment cost.
第1図は汚泥滞留時間と濃縮汚泥濃度との関係
を示す特性図、第2図は汚泥中炭酸ガス濃度と汚
泥浮上時間との関係を示す特性図、第3図、第5
図及び第6図はそれぞれ本発明の一実施例を示す
構成図、第4図及び第7図は排出制御装置の詳細
構成図である。
5……汚泥曝気槽、6……曝気用ブロワー、1
1……炭酸ガス濃度計、12……演算装置、13
……制御装置、9……濃縮槽、10……濃縮汚泥
ポンプ。
Figure 1 is a characteristic diagram showing the relationship between sludge retention time and thickened sludge concentration, Figure 2 is a characteristic diagram showing the relationship between carbon dioxide concentration in sludge and sludge floating time, Figures 3 and 5
6 and 6 are block diagrams showing one embodiment of the present invention, respectively, and FIGS. 4 and 7 are detailed block diagrams of the emission control device. 5...Sludge aeration tank, 6...Aeration blower, 1
1... Carbon dioxide concentration meter, 12... Arithmetic device, 13
...Control device, 9...Thickening tank, 10...Thickened sludge pump.
Claims (1)
と、該沈殿池から引き抜いた汚泥をさらに沈降濃
縮させる濃縮槽と、該濃縮槽に供給する汚泥を曝
気する汚泥曝気装置と、該汚泥曝気装置の曝気排
ガス中に含有する特定成分のガス濃度を検出する
ガス濃度計とを具備し、該ガス濃度計の検出値に
応じて前記濃縮槽からの引き抜き汚泥量を制御す
ることを特徴とする濃縮槽の排泥制御装置。1. A sedimentation tank that sediments and concentrates suspended solids from wastewater, a thickening tank that further sediments and thickens the sludge extracted from the sedimentation tank, a sludge aeration device that aerates the sludge supplied to the thickening tank, and the sludge aeration device. and a gas concentration meter that detects the gas concentration of a specific component contained in the aeration exhaust gas, and the amount of sludge drawn from the concentration tank is controlled according to the detected value of the gas concentration meter. Tank sludge control device.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6526382A JPS58183914A (en) | 1982-04-21 | 1982-04-21 | Apparatus for controlling waste sludge of concentration tank |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6526382A JPS58183914A (en) | 1982-04-21 | 1982-04-21 | Apparatus for controlling waste sludge of concentration tank |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58183914A JPS58183914A (en) | 1983-10-27 |
| JPS6154445B2 true JPS6154445B2 (en) | 1986-11-22 |
Family
ID=13281850
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6526382A Granted JPS58183914A (en) | 1982-04-21 | 1982-04-21 | Apparatus for controlling waste sludge of concentration tank |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58183914A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011200792A (en) * | 2010-03-25 | 2011-10-13 | Kobelco Eco-Solutions Co Ltd | Apparatus and method for anaerobic treatment |
| JP7005956B2 (en) * | 2017-06-20 | 2022-01-24 | 栗田工業株式会社 | Sludge treatment management method |
-
1982
- 1982-04-21 JP JP6526382A patent/JPS58183914A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58183914A (en) | 1983-10-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100360438C (en) | Method and device for biological treatment of water regulated by aeration and by activated sludge | |
| US8916046B2 (en) | Method for controlling oxygen supply for treating wastewater, and facility for implementing same | |
| CN111039395A (en) | Accurate aeration control method and system | |
| JP2002126779A (en) | Sludge treatment method and apparatus used therefor | |
| JP2003136086A (en) | Sewage treatment plant water quality control device | |
| JPS6154445B2 (en) | ||
| JPH0938690A (en) | Flocculant injection control method in water treatment | |
| JP2004249252A (en) | Wastewater treatment method | |
| JP2023543902A (en) | A method for treating wastewater by compacting sludge in a batch activated sludge reactor | |
| JP3388293B2 (en) | Biological nitrification and denitrification method for night soil | |
| JP4543649B2 (en) | Nitrification processing method and apparatus | |
| JPH067792A (en) | Organic wastewater treatment method and methane fermentation treatment device | |
| JPH0938682A (en) | Biological water treatment method | |
| JPH035876B2 (en) | ||
| JPH09314187A (en) | Biological treatment equipment | |
| JPH05253597A (en) | Nitrification reaction control device in activated sludge treatment | |
| JPS6115793A (en) | Treatment of organic waste water | |
| CN220867200U (en) | Carbon source adding early warning and monitoring system for CASS pool | |
| JPH07116684A (en) | Control method of intermittent aeration type activated sludge method | |
| JPH11290888A (en) | Biological water treatment method and control device therefor | |
| JPH10263571A (en) | Method for catalytically oxidizing waste water | |
| JPH10323688A (en) | How to remove phosphorus from wastewater | |
| JPS58186405A (en) | Control device for gravity settling thickener | |
| JP2000084585A (en) | Operation control method of aeration device and sludge extraction pump | |
| JP2001029991A (en) | Water treatment method |