JPS6322876B2 - - Google Patents
Info
- Publication number
- JPS6322876B2 JPS6322876B2 JP24327684A JP24327684A JPS6322876B2 JP S6322876 B2 JPS6322876 B2 JP S6322876B2 JP 24327684 A JP24327684 A JP 24327684A JP 24327684 A JP24327684 A JP 24327684A JP S6322876 B2 JPS6322876 B2 JP S6322876B2
- Authority
- JP
- Japan
- Prior art keywords
- phosphorus
- bottom sludge
- filled
- elution
- phosphate rock
- 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
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 38
- 239000011574 phosphorus Substances 0.000 claims description 38
- 229910052698 phosphorus Inorganic materials 0.000 claims description 38
- 239000010802 sludge Substances 0.000 claims description 32
- 238000010828 elution Methods 0.000 claims description 11
- 239000002367 phosphate rock Substances 0.000 claims description 10
- 239000008187 granular material Substances 0.000 claims description 7
- 239000002893 slag Substances 0.000 claims description 7
- 238000001179 sorption measurement Methods 0.000 claims description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 108010082455 Sebelipase alfa Proteins 0.000 claims description 2
- 229940041615 kanuma Drugs 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- 239000000395 magnesium oxide Substances 0.000 claims description 2
- 239000002689 soil Substances 0.000 claims description 2
- 239000011236 particulate material Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 235000015097 nutrients Nutrition 0.000 description 8
- 238000012851 eutrophication Methods 0.000 description 6
- 239000010881 fly ash Substances 0.000 description 5
- 239000012071 phase Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000006228 supernatant Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 239000005416 organic matter Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000002779 inactivation Effects 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 241001455273 Tetrapoda Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/28—Treatment of water, waste water, or sewage by sorption
- C02F1/281—Treatment of water, waste water, or sewage by sorption using inorganic sorbents
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Organic Chemistry (AREA)
- Removal Of Specific Substances (AREA)
- Water Treatment By Sorption (AREA)
Description
近年、湖沼、海域、河川などで停滞性水域にお
ける富栄養化が重大な社会問題となつてきてい
る。富栄養化の主原因物質は、栄養塩あるいは有
機物と見られているが、このうちリンは富栄養化
の制限因子と言われている。
富栄養化防止策としては、水域に流入する栄養
塩、有機物の除去が重要であるとともに、水域内
の底部汚泥中に蓄積した栄養塩の溶出防止やこの
溶出したリンを除去することも重要な対策の一つ
である。
底部汚泥中の栄養塩の対策としては、底部汚泥
の浚渫、底部汚泥の被覆、栄養塩の薬剤による不
活性化などがあるが、底部汚泥の浚渫は、底部汚
泥の除去に多大な費用を要するとともに、除去し
た底部汚泥の処理、処分がやつかいな問題となつ
ていた。
栄養塩の薬剤による不活性化は、主としてAl
塩を水域に直接添加する方法があるが、薬品使用
量が多大であること、およびこれらの薬剤の生態
系への影響が問題となつている。
底部汚泥の被覆は、フライアツシユ、砂、プラ
スチツクシートなどで底部汚泥上を被覆するもの
であるが、砂やプラスチツクシートは栄養塩の溶
出防止効果がほとんどなく、フライアツシユはリ
ンの溶出防止に効果があるが、長期間経過すると
底部汚泥より発生する気泡によりフライアツシユ
層が破壊され、栄養塩、有機物の溶出が起つてし
まう。またフライアツシユは沈降速度が遅いの
で、底部汚泥を被覆する層を形成するのに長期間
を有し、逆に水域の汚濁の要因となつてしまうの
である。
さらに、このフライアツシユは、リン除去能力
が低下しても、回収して再生することは困難で、
再度添加する以外に方法がない。
本発明は、上記の問題点を解決し、底部汚泥か
らのリンの溶出防止及び溶出したリンの除去をき
わめて効率よく行う方法に関するものである。す
なわち、本発明は、湖沼等の底部汚泥から溶出し
たたリンの除去、あるいはリンの溶出を防止する
にあたり、該底部汚泥上および/または底部汚泥
上部の液相中にリン吸着能力を有する粒状物を充
てんした網状あるいは多孔物構造体を存在せしめ
ることを特徴とする液中のリンの除去方法であ
る。
次に本発明の実施態様を図面に基づいて説明す
る。第1図は、富栄養化の進行している湖の底部
汚泥1上に、リン鉱石2を充てんした直方体の網
状構造物3を設置した場合を示すものである。該
構造物は、直方体の網状構造物3にリン鉱石2を
充てんした後、通常はクレーン等により、底部汚
泥上に設置する。
第2図は、構造物として表面に孔をあけた多孔
質状構造物3′を用いた例を示し、さらに、第3
図は網状構造物として球形のものを用いた例を示
すものである。
第1図、第2図および第3図に示すものは、主
として底部汚泥からのリンの溶出をも防止しうる
ものである。第1,2,3図に示すように底部汚
泥1上に設置する場合、水域の底部汚泥上に均等
にかつ短時間で設置することができる。また、リ
ン鉱石は網状、あるいは多孔質状構造物に入つて
いるため、長期間使用しても底部汚泥から発生す
るガスにより、充てん層が乱されることはない。
第4図は、第3図に示す球体の網状構造物内3
にリンの吸着能力を有する吸着体を収納すると共
に空気相4を設けた例で、水域内に浮遊せしめて
底部汚泥から溶出したリンを除去するためのもの
である。
通常、水域の深水層にDOを供給するために空
気揚水筒などが使用されているが、ここで第4図
に示す如き球体を空気揚水筒で循環すれば、DO
の供給と同時に、リンの除去も可能である。
第5図は、筒状の網状構造物中にリンの吸着体
を入れたものを示し、第6図は第5図に示す構造
体中に更に空気相を設けた場合の内部構造を示
す。
第1図ないし第5図に示す各構造物は回収が容
易で、リン除去能力が低下した場合、再充てんが
可能である。
また、回収した構造物を酸やアルカリに浸漬す
ることによりリン除去能力の回復が可能である。
また、上記の構造物を護岸提防やテトラポツト
として利用すれば、湾内の富栄養化防止に寄与で
き、これは好ましい適用例の一つである。
リン吸着能力を有する粒状物とは、天然のリン
鉱石、鹿沼土が生態系にとつては良く、また、リ
ン除去能力からみれば骨炭、スラグ、軽焼マグネ
シアが優れている。スラグとしては、転炉、高
炉、水砕スラグの何れを用いてもよい。
CaOを多く含有するスラグは、リンをリン酸カ
ルシウムの形で沈殿する効果を有するので、リン
の不活性化も可能である。
粒状物の粒径は、細かい方が好ましく、実用的
には0.4〜0.6mm程度で、かつ網状及び多孔構造体
の網目の大きさおよび各孔径は、粒状物が流出し
ないような大きさ並びに径とすることが必要であ
る。
本発明の実施例を以下に示す。
実施例 1
径100mm×800mm高さの円筒状の透明アクリルカ
ラムに、広島湾の底部汚泥を300mm厚に充てんし、
その上に0.4mm〜0.6mmのリン鉱石を200mm厚さに
充てんした円筒状の網状構造物(60メツシユ)を
設置し、上澄水を嫌気状態にして、リンの溶出速
度を求めた。同じ底部汚泥を充てんして、網状構
造物にリン鉱石の代りに骨炭(0.4〜0.6mm)を入
れた場合、転炉スラグ(0.4〜0.6mm)を入れた場
合についてリン溶出速度を求め、網状構造物を設
置しない場合と比較した。
表―1に処理結果を示す。表―1の結果からわ
かるように実施例では、いずれもリン溶出防止効
果があり、中でも転炉スラグが良好であつた。
In recent years, eutrophication in stagnant water bodies such as lakes, oceans, and rivers has become a serious social problem. The main causes of eutrophication are thought to be nutrient salts or organic matter, but phosphorus is said to be the limiting factor for eutrophication. As measures to prevent eutrophication, it is important to remove nutrients and organic matter that flow into water bodies, and it is also important to prevent the elution of nutrients accumulated in the bottom sludge in water bodies and to remove this eluted phosphorus. This is one of the countermeasures. Countermeasures against nutrient salts in the bottom sludge include dredging the bottom sludge, coating the bottom sludge, and inactivating the nutrient salts with chemicals, but dredging the bottom sludge requires a large amount of cost to remove the bottom sludge. At the same time, the treatment and disposal of the removed bottom sludge has become a difficult problem. Pharmaceutical inactivation of nutrients is mainly due to Al
There is a method of directly adding salt to water bodies, but problems arise due to the large amount of chemicals used and the impact of these chemicals on the ecosystem. Bottom sludge is coated with fly ash, sand, plastic sheets, etc., but sand and plastic sheets have little effect on preventing the elution of nutrients, while fly ash is effective in preventing the elution of phosphorus. However, over a long period of time, air bubbles generated from the bottom sludge destroy the flyash layer, causing leaching of nutrients and organic matter. Furthermore, since fly ash has a slow sedimentation rate, it takes a long time to form a layer that covers the bottom sludge, which conversely becomes a factor in the pollution of water bodies. Furthermore, even if the phosphorus removal ability of this flyash decreases, it is difficult to recover and regenerate it.
There is no other way than to add it again. The present invention solves the above-mentioned problems and relates to a method for extremely efficiently preventing the elution of phosphorus from the bottom sludge and removing the eluted phosphorus. That is, in order to remove phosphorus eluted from bottom sludge of lakes and marshes, or to prevent phosphorus elution, the present invention provides granular materials having phosphorus adsorption ability on the bottom sludge and/or in the liquid phase above the bottom sludge. This is a method for removing phosphorus from a liquid, which is characterized by the presence of a network or porous structure filled with phosphorus. Next, embodiments of the present invention will be described based on the drawings. FIG. 1 shows a case where a rectangular parallelepiped network structure 3 filled with phosphate rock 2 is installed on bottom sludge 1 of a lake where eutrophication is progressing. After filling the rectangular parallelepiped network structure 3 with phosphate rock 2, the structure is usually installed on the bottom sludge using a crane or the like. FIG. 2 shows an example in which a porous structure 3' with holes formed on the surface is used as the structure, and a third porous structure 3' is used as the structure.
The figure shows an example in which a spherical net structure is used. The devices shown in FIGS. 1, 2, and 3 can also mainly prevent phosphorus elution from the bottom sludge. When installing on the bottom sludge 1 as shown in Figures 1, 2, and 3, it can be installed evenly on the bottom sludge of a water body in a short time. Furthermore, since the phosphate rock is contained in a net-like or porous structure, the packed layer will not be disturbed by gas generated from the bottom sludge even after long-term use. Figure 4 shows the inside of the spherical network structure shown in Figure 3.
This is an example in which an adsorbent having the ability to adsorb phosphorus is housed in the sludge and an air phase 4 is provided, and the phosphorus is suspended in a water body to remove phosphorus eluted from the bottom sludge. Normally, an air pumping tube or the like is used to supply DO to the deep water layer of a body of water, but if a sphere like the one shown in Figure 4 is circulated in the air pumping tube, the DO
It is possible to simultaneously supply phosphorus and remove phosphorus. FIG. 5 shows a cylindrical network structure in which a phosphorus adsorbent is placed, and FIG. 6 shows the internal structure of the structure shown in FIG. 5 in which an air phase is further provided. The structures shown in Figures 1-5 are easily retrievable and can be refilled if their phosphorus removal capacity decreases. Furthermore, the phosphorus removal ability can be restored by immersing the recovered structure in acid or alkali. Further, if the above-mentioned structure is used as a sea wall or a tetrapod, it can contribute to preventing eutrophication in the bay, and this is one of the preferred application examples. Regarding granular materials having phosphorus adsorption ability, natural phosphate rock and Kanuma soil are good for the ecosystem, and bone charcoal, slag, and light burnt magnesia are excellent in terms of phosphorus removal ability. As the slag, any of converter furnace, blast furnace, and granulated slag may be used. Slag containing a large amount of CaO has the effect of precipitating phosphorus in the form of calcium phosphate, so that phosphorus inactivation is also possible. The particle size of the granules is preferably finer, and is practically about 0.4 to 0.6 mm, and the mesh size and each pore size of the network and porous structure should be such that the granules do not flow out. It is necessary to do so. Examples of the present invention are shown below. Example 1 A cylindrical transparent acrylic column with a diameter of 100 mm and a height of 800 mm was filled with bottom sludge from Hiroshima Bay to a thickness of 300 mm.
A cylindrical network structure (60 meshes) filled with 0.4 mm to 0.6 mm phosphate rock to a thickness of 200 mm was placed on top of the structure, and the supernatant water was placed in an anaerobic state to determine the phosphorus elution rate. The same bottom sludge is filled, and the phosphorus elution rate is determined when bone coal (0.4 to 0.6 mm) is added instead of phosphate rock to the net structure, and when converter slag (0.4 to 0.6 mm) is added to the net structure. A comparison was made with the case where no structure was installed. Table 1 shows the processing results. As can be seen from the results in Table 1, all of the examples had the effect of preventing phosphorus elution, and converter slag was especially effective.
【表】
実施例 2
実施例1において、リン鉱石を網状構造物に入
れた場合とリン鉱石を直接充てんした場合とを比
較した。結果を表―2に示す。[Table] Example 2 In Example 1, a comparison was made between the case where phosphate rock was placed in the network structure and the case where phosphate rock was directly filled. The results are shown in Table-2.
【表】【table】
【表】
表―2に示すように、比較例のリン鉱石を直接
充てんした場合、充てん時に上澄水の濁度が上昇
し、かつ30日後に底部汚泥から発生するガスによ
り充てん層が乱れ、上澄中の濁度及びリン溶出速
度が上昇した。
一方、実施例では、充てん時の上澄水の濁度は
低く、底部汚泥から発生するガスによる充てん層
の乱れはなかつた。
実施例 3
100mm〓×1600mmHのアクリル製円筒カラム2本
に、中海の底部汚泥を300mmの厚さに充てんし、
その中に中海の底部汚泥の上部水を130mmの厚さ
にはつて、嫌気状態とした。一方のカラムに球状
の網状構造物(網はステンレス製の径40mm、60メ
ツシユの孔をあけたもの)に、0.4〜0.6mmの骨炭
を充てんし、内部にピンポン玉を入れたものを2
個入れ、上澄水のリン濃度を測定した。[Table] As shown in Table 2, when the phosphate rock of the comparative example was directly filled, the turbidity of the supernatant water increased at the time of filling, and after 30 days, the filled layer was disturbed by the gas generated from the bottom sludge, and the The turbidity and phosphorus elution rate in the clear fluid increased. On the other hand, in the example, the turbidity of the supernatant water at the time of filling was low, and the filled layer was not disturbed by the gas generated from the bottom sludge. Example 3 Two acrylic cylindrical columns measuring 100 mm × 1600 mmH were filled with Nakaumi bottom sludge to a thickness of 300 mm.
The top water of Nakaumi's bottom sludge was poured into the tank to a thickness of 130 mm to create an anaerobic condition. In one column, a spherical mesh structure (the mesh is made of stainless steel with a diameter of 40 mm and 60 mesh holes) is filled with bone charcoal of 0.4 to 0.6 mm, and a ping pong ball is placed inside.
The phosphorus concentration of the supernatant water was measured.
【表】
* 球状の網状構造物を入れない場合
結果は表―3に示すとおり本発明はリン除去効
率が大である。[Table] * When no spherical network structure is added As shown in Table 3, the present invention has a high phosphorus removal efficiency.
第1図、第2図、第3図及び第5図は夫々本発
明で用いるリン吸着能を有する粒状物を充てんし
た網状ないしは多孔質構造物の概略図を示し、第
4図及び第6図は、夫々第3図及び第5図に示す
構造体中に更に空気相を設けた例を示すための概
略図である。
1…底部汚泥、2…リン吸着能を有する粒状
物、3…網状構造体、3′…小孔を設けた構造体、
4…空気相。
FIGS. 1, 2, 3 and 5 are schematic views of a network or porous structure filled with granules having phosphorus adsorption ability used in the present invention, and FIGS. 5A and 5B are schematic diagrams illustrating an example in which an air phase is further provided in the structures shown in FIGS. 3 and 5, respectively. 1... Bottom sludge, 2... Granular material having phosphorus adsorption ability, 3... Network structure, 3'... Structure provided with small holes,
4...Air phase.
Claims (1)
あるいはリンの溶出を防止するにあたり、該底部
汚泥上および/または底部汚泥上部の液相中にリ
ン吸着能力を有する粒状物を充てんした網状ある
いは多孔物構造物を存在せしめることを特徴とす
る液中のリン除去方法。 2 リン吸着能力を有する粒状物がリン鉱石、鹿
沼土、骨炭、スラグまたは軽焼マグネシアである
特許請求の範囲第1項記載の液中のリン除去方
法。[Claims] 1. Removal of phosphorus eluted from bottom sludge of lakes, marshes, etc.
Alternatively, in order to prevent the elution of phosphorus, a network or porous structure filled with granular materials having phosphorus adsorption ability is present on the bottom sludge and/or in the liquid phase above the bottom sludge. How to remove phosphorus. 2. The method for removing phosphorus from a liquid according to claim 1, wherein the particulate material having phosphorus adsorption ability is phosphate rock, Kanuma soil, bone charcoal, slag, or lightly burnt magnesia.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24327684A JPS61125483A (en) | 1984-11-20 | 1984-11-20 | Method for removing phosphoric acid in liquid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24327684A JPS61125483A (en) | 1984-11-20 | 1984-11-20 | Method for removing phosphoric acid in liquid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61125483A JPS61125483A (en) | 1986-06-13 |
| JPS6322876B2 true JPS6322876B2 (en) | 1988-05-13 |
Family
ID=17101456
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24327684A Granted JPS61125483A (en) | 1984-11-20 | 1984-11-20 | Method for removing phosphoric acid in liquid |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61125483A (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02198690A (en) * | 1989-01-30 | 1990-08-07 | Ebara Infilco Co Ltd | Phosphorus removing agent and production thereof |
| JPH0330894A (en) * | 1989-06-29 | 1991-02-08 | Shimizu Corp | Method for preventing contamination of lake and marsh and reservoir |
| JPH0368489A (en) * | 1989-08-08 | 1991-03-25 | Damu Suigenchi Kankyo Seibi Center | Device for removing phosphorus in water |
| KR100365893B1 (en) * | 2000-02-15 | 2002-12-26 | 주식회사 포스렉 | Matter For Improving Organism Of The Sea Bottom And Preventing Red Tide In The Fish Farm And Coastal Fishing Ground |
| JP2006341226A (en) * | 2005-06-10 | 2006-12-21 | Nippon Steel Corp | How to remove phosphorus from water |
| JP5020397B1 (en) * | 2011-06-28 | 2012-09-05 | 株式会社アサカ理研 | Water treatment system and water treatment method |
| JP6197095B1 (en) * | 2016-12-14 | 2017-09-13 | 新日鉄住金エンジニアリング株式会社 | Method for recovering phosphorus in treated water |
-
1984
- 1984-11-20 JP JP24327684A patent/JPS61125483A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61125483A (en) | 1986-06-13 |
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