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JPS5940488B2 - Filter media and filtration methods for water treatment - Google Patents
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JPS5940488B2 - Filter media and filtration methods for water treatment - Google Patents

Filter media and filtration methods for water treatment

Info

Publication number
JPS5940488B2
JPS5940488B2 JP57118974A JP11897482A JPS5940488B2 JP S5940488 B2 JPS5940488 B2 JP S5940488B2 JP 57118974 A JP57118974 A JP 57118974A JP 11897482 A JP11897482 A JP 11897482A JP S5940488 B2 JPS5940488 B2 JP S5940488B2
Authority
JP
Japan
Prior art keywords
filtration
sand
polymer
water treatment
water
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
Application number
JP57118974A
Other languages
Japanese (ja)
Other versions
JPS5910318A (en
Inventor
亮吾 築坂
誠 目次
宜二 井村
行夫 森瀬
薫 菊井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kurimoto Iron Works Ltd
Original Assignee
Kurimoto Iron Works Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kurimoto Iron Works Ltd filed Critical Kurimoto Iron Works Ltd
Priority to JP57118974A priority Critical patent/JPS5940488B2/en
Publication of JPS5910318A publication Critical patent/JPS5910318A/en
Publication of JPS5940488B2 publication Critical patent/JPS5940488B2/en
Expired legal-status Critical Current

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  • Water Treatment By Sorption (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Filtering Materials (AREA)
  • Filtration Of Liquid (AREA)

Description

【発明の詳細な説明】 本発明は優れたろ過性能を有する水処理用ろ材及びそれ
を用いたろ過方式に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a water treatment filter medium having excellent filtration performance and a filtration method using the same.

一般に、下水等の有機物含有廃水の廃水処理は、BOD
の対象である有機物質、窒素化合物等を除去するために
、活性汚泥法等の生物処理法を施し、次にこの処理水を
沈殿池、浮上槽等により沈殿物を分離した後、砂ろ過性
により微細な生物片等の懸濁物(Suspended
Sol id1以下ssと略す。
Generally, wastewater treatment of organic matter-containing wastewater such as sewage is carried out using BOD
In order to remove organic substances, nitrogen compounds, etc., which are the target of the Suspended substances such as finer biological fragments
Solid id1 and below are abbreviated as ss.

)をろ去してSS濃度を5〜3000pI)m程度に浄
化する方法が採られている。
) is removed by filtration to purify the SS concentration to about 5 to 3000 pI)m.

また、処理水を種々の目的に再利用するためSS濃度を
1ppI[1以下にしたい場合には、砂ろ過層に凝集剤
を添加して微細なSSを凝集させ大粒化してから砂ろ過
に供する等の方法が採られている。
In addition, if you want to reduce the SS concentration to 1 ppI or less in order to reuse the treated water for various purposes, add a flocculant to the sand filtration layer to flocculate fine SS to make them larger particles before applying them to sand filtration. The following methods have been adopted.

上記の如き水処理における砂ろ過の機構は、水に浮遊す
るSSを篩で掬い上げて取り除く方法と同様である。
The mechanism of sand filtration in water treatment as described above is similar to the method of scooping up SS floating in water with a sieve and removing it.

即ち、砂層の間隙にSSを捕捉せしめて、水のみを通過
させる仕組である。
That is, the system traps SS in the gaps in the sand layer and allows only water to pass through.

砂ろ過において砂の粒径は、篩目に相当し、処理水中の
SSをより多く捕捉するためには、より細かな砂を用い
ることが必要となる。
In sand filtration, the grain size of sand corresponds to sieve size, and in order to capture more SS in the treated water, it is necessary to use finer sand.

しかしながら、砂がより細かくなるにつれてSSの捕捉
性能が高められる反面、ろ過抵抗の増大及びろ過速度の
低下がもたらされるだけでなく、ろ過層の間隙径が狭く
なるため、SSによるろ過層の目詰りが早くなり、洗浄
までのろ遅時間(ろ過サイクル)が短くなるという大き
な欠点が生じる。
However, as the sand becomes finer, the trapping performance of SS increases, but it not only increases the filtration resistance and decreases the filtration rate, but also causes the filtration layer to become clogged with SS because the pore size of the filtration layer becomes narrower. The major drawback is that the filtration time (filtration cycle) until cleaning is shortened.

従来、上記欠点を改善するため、粒径の粗い砂と細かい
沙を併用し、粒径の粗い砂を流水入口側に配夕1ルて、
大なるSSを流水入口側でまず捕捉し、ろ過層のSS保
留空間を最大限に有効利用する方法が採られている。
Conventionally, in order to improve the above drawbacks, coarse sand and fine sand were used together, and the coarse sand was placed on the water inlet side.
A method is adopted in which large SS is first captured on the water inlet side, and the SS retention space in the filtration layer is utilized as effectively as possible.

しかしながら、このようなろ過方法においては、上記欠
点の改善がなお充分でなく、また洗浄操作後、自動的に
元の配列に復元せしめるためには、比重が大きく異なる
砂を配合しなければならずろ材が高価なものとなるとい
う難点もある。
However, in this filtration method, the above-mentioned drawbacks are still not sufficiently improved, and in order to automatically restore the original arrangement after the cleaning operation, it is necessary to mix sands with significantly different specific gravity. Another drawback is that the filter media is expensive.

本発明者は、上記現状に鑑めで、SS捕捉性能が高く、
ろ過サイクルが長く、ろ過抵抗が小さく、かつ安価な水
処理用ろ材を開発するため鋭意研究した結果、ろ過層を
カチオン性ポリマーで被覆処理することにより目的が達
成されることを見出し、本発明を完成するに至った。
In view of the above-mentioned current situation, the present inventor has realized that the SS capture performance is high,
As a result of intensive research to develop a filter medium for water treatment that has a long filtration cycle, low filtration resistance, and is inexpensive, it was discovered that the objective could be achieved by coating the filtration layer with a cationic polymer, and the present invention was developed. It was completed.

即ち本発明は、ろ過層をカチオン性ポリマーで被覆した
ことを特徴とする水処理用ろ材、及びろ、過層をカチオ
ン性ポリマーで被覆してなる水処理用ろ材を用いて上向
流方式でろ過することを特徴とするろ過方法に係る。
That is, the present invention provides a water treatment filter medium characterized in that a filtration layer is coated with a cationic polymer, and a water treatment filter medium in which a filter layer is coated with a cationic polymer. It relates to a filtration method characterized by filtration.

本発明におけるろ過層としては、通常この種の用途に用
いられるものをいずれも使用出来、例えば川砂、海砂、
ケイ砂等を挙げることが出来る。
As the filtration layer in the present invention, any material that is normally used for this type of purpose can be used, such as river sand, sea sand,
Examples include silica sand.

粒径は、特に限定されるものではないが、0.1〜5朋
程度であるのが適当である。
Although the particle size is not particularly limited, it is suitably about 0.1 to 5 mm.

また、本発明で用いるカチオン性ポリマーは、粒子荷電
がカチオン性であるポリマー、及びチオン構造を分子中
に有するポリマーであって、砂に良く固着し、かつ水に
難溶性(JISK−6828による六回溶分試験におい
て、六回溶分が5係以下)の皮膜を形成するものである
In addition, the cationic polymer used in the present invention is a polymer whose particle charge is cationic and a polymer having a cationic structure in the molecule, which adheres well to sand and is sparingly soluble in water (according to JIS K-6828). In the twice-dissolved portion test, it forms a film with a six-times dissolved portion of 5 or less.

その様なカチオン性ポリマーとしては、以下のものを挙
げることが出来る。
Examples of such cationic polymers include the following.

尚、以下の例示において(メタ)アクリレートとあるの
は、アクリレート及びメタアクリレートの双方を示すも
のとする。
In the following examples, (meth)acrylate refers to both acrylate and methacrylate.

(メタ)アクリルとあるものも同様である。(1)
メチル(メタ)アクリレート、エチル(メタ)アクリレ
ート、n−プロピル(メタ)アクリレート、イソプロピ
ル(メタ)アクリレート、n−ブチル(メタ)アクリレ
ート、tert−ブチル(メタ)アクリレート、2−エ
チルヘキシル(メタ)アクリレート等の(メタ)アクリ
ル酸エステル類、(メタ)アクリル酸アミド及びそのメ
チロール化物、スチレン、ビニルトルエン、α−メチル
スチレン等のスチレン系モノマー類、酢酸ビニル、プロ
ピオン酸ビニル等の脂肪酸ビニルエステル類、アクリロ
ニトリル、エチレン、塩化ビニル、塩化ビニリデン、ブ
タジェン、イソプレン、クロロプレン等のビニル単量体
(Aとする)の少なくとも1種を2,2′−アゾビス(
2−アミノジプロパン)塩酸塩等のカチオン性開始剤を
用いて重合することにより、ポリマー末端にカチオン構
造を導入したポリマー。
The same is true for (meth)acrylic. (1)
Methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, n-butyl (meth)acrylate, tert-butyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, etc. (meth)acrylic acid esters, (meth)acrylic acid amide and its methylolated products, styrenic monomers such as styrene, vinyltoluene and α-methylstyrene, fatty acid vinyl esters such as vinyl acetate and vinyl propionate, acrylonitrile , ethylene, vinyl chloride, vinylidene chloride, butadiene, isoprene, chloroprene, etc.
A polymer with a cationic structure introduced at the polymer end by polymerization using a cationic initiator such as 2-aminodipropane) hydrochloride.

(2)上記ビニル単量体(5)に、ジメチルアミノエチ
ル(メタ)アクリレート、ジエチルアミノエチル(メタ
)アクリレート、t−ブチルアミノエチル(メタ)アク
リレート、2−アミノエチルビニルエーテル、ビニルピ
リジン等のアミン基を有するビニル単量体の少なくとも
1種を1モルφ以上共重合したポリマー。
(2) The vinyl monomer (5) has an amine group such as dimethylaminoethyl (meth)acrylate, diethylaminoethyl (meth)acrylate, t-butylaminoethyl (meth)acrylate, 2-aminoethyl vinyl ether, vinylpyridine, etc. A polymer obtained by copolymerizing at least one vinyl monomer having 1 mole φ or more.

(3)水溶性のカチオン性熱硬化性樹脂水溶液中で、上
記ビニル単量体囚を乳化重合して得られるポリマー(特
公昭46−22922の製造法)。
(3) A polymer obtained by emulsion polymerization of the above vinyl monomer in an aqueous solution of a water-soluble cationic thermosetting resin (manufacturing method disclosed in Japanese Patent Publication No. 46-22922).

(4) カチオン性オリゴマー水溶液中で、上記ビニ
ル単量体(5)を乳化重合して得られるポリマー(特開
昭54−21485の製造法)。
(4) A polymer obtained by emulsion polymerization of the vinyl monomer (5) in an aqueous cationic oligomer solution (manufacturing method disclosed in JP-A-54-21485).

(5)カチオン性ユリア樹脂、カチオン性メラミン樹脂
、カチオン性ポリュリアーポリアミド共縮合樹脂、カチ
オン性エポキシ樹脂等の熱硬化性ポリマー。
(5) Thermosetting polymers such as cationic urea resins, cationic melamine resins, cationic polyurea polyamide cocondensation resins, and cationic epoxy resins.

上記のカチオン性ポリマーの内、通常、(1)及び(2
)は固体、エマルジョン又は有機溶剤の溶液として、(
3)及び(4)はエマルジョンとして、並びに(5)は
水溶液として用い、砂に被覆処理する。
Among the above cationic polymers, usually (1) and (2)
) as a solid, emulsion or solution in an organic solvent (
3) and (4) are used as emulsions, and (5) is used as an aqueous solution to coat sand.

本発明におけるカチオン性ポリマーの被覆量としては、
特に限定されることなく広い範囲から選択され、また用
いた該ポリマーの種類によっても変動するが、通常ろ過
層100重量部に対して0.005〜10重量部程度好
ましくは0.01〜5重量部である。
The coating amount of the cationic polymer in the present invention is as follows:
It is selected from a wide range without particular limitation, and varies depending on the type of the polymer used, but it is usually about 0.005 to 10 parts by weight, preferably 0.01 to 5 parts by weight, based on 100 parts by weight of the filtration layer. Department.

0.005重量部未満ては本発明所期の効果が得られず
、また10重量部を越えて使用してもより以上の効果は
望めず経済的に好ましくない。
If the amount is less than 0.005 parts by weight, the desired effect of the present invention cannot be obtained, and if it is used in excess of 10 parts by weight, no further effect can be expected and it is not economically preferable.

本発明においてカチオン性ポリマーを砂に被覆処理する
方法は、使用する該ポリマーの性状により公知の方法か
ら適宜選択すれば良い。
In the present invention, the method for coating sand with a cationic polymer may be appropriately selected from known methods depending on the properties of the polymer used.

該ポリマーの性状に応じた被覆処理方法の例を以下に示
す。
Examples of coating treatment methods depending on the properties of the polymer are shown below.

使用する該ポリマーが、エマルジョン若しくは熱硬化性
樹脂の水溶液の場合には、該ポリマーを砂に添加後、均
一に攪拌混合しながら加熱して、水を蒸発除去し、砂粒
表面上に該ポリマーの皮膜を形成せしめる。
When the polymer used is an emulsion or an aqueous solution of a thermosetting resin, the polymer is added to the sand and heated while stirring and mixing uniformly to evaporate the water and deposit the polymer on the surface of the sand grains. Forms a film.

加熱温度は、該ポリマーの硬化温度及び水分量によって
左右されるが、通常100〜180℃程度である。
The heating temperature depends on the curing temperature and moisture content of the polymer, but is usually about 100 to 180°C.

また、使用する該ポリマーが固体の場合には、砂を予め
加熱して該ポリマーの融点以上とし、これに該ポリマー
を添加後、均一に攪拌混合しながら、砂粒表面上に該ポ
リマーの皮膜を形成せしめる。
In addition, when the polymer used is solid, the sand is heated in advance to a temperature above the melting point of the polymer, and after the polymer is added thereto, a film of the polymer is formed on the surface of the sand grains while stirring and mixing uniformly. Form.

固体ポリマーがベンゼン アセトン、ヘキサン等の有機
溶剤に可溶である場合には、有機溶剤に溶解した該ポリ
マーを砂に添加後、均一に攪拌混合しながら、加熱して
、有機溶剤を蒸発除去し、砂粒表面上に該ポリマーの皮
膜を形成しても良い。
When the solid polymer is soluble in an organic solvent such as benzene, acetone, or hexane, the polymer dissolved in the organic solvent is added to the sand, and the organic solvent is evaporated off by heating while stirring and mixing uniformly. , a film of the polymer may be formed on the surface of the sand grains.

本発明において、ろ過砂にカチオン性ポリマーを被覆処
理する場合の機器としては、加熱装置を備えたリボンブ
レンダー、プラネタリ−ミキサー、ヘンシュル型高速ミ
キサー、ソリッドエアー型流動乾燥器、その他攪拌混合
と加熱の両機能を有する機器であればいずれも使用でき
る。
In the present invention, equipment for coating filter sand with a cationic polymer includes a ribbon blender equipped with a heating device, a planetary mixer, a Henschel type high-speed mixer, a solid air type fluidized dryer, and other devices capable of stirring, mixing and heating. Any device that has both functions can be used.

斯くして得られる本発明水処理用ろ材を用いてろ過する
方法としては、下向流方式及び上向流方式のいずれも採
用し得るが、前者の場合は後者に比べてろ過抵抗が大き
く、目詰りが早いので後者の方式が特に有効である。
As a method of filtration using the thus obtained filter medium for water treatment of the present invention, both a downward flow method and an upward flow method can be adopted, but in the case of the former, the filtration resistance is greater than the latter; The latter method is particularly effective because clogging occurs quickly.

本発明水処理用ろ材を用いて上向流方式による急速砂ろ
過性を図面を用いて説明する。
The rapid sand filtration performance by the upward flow method using the water treatment filter medium of the present invention will be explained with reference to the drawings.

第1図は、本発明水処理用ろ材を用いてろ過する場合に
使用するろ過塔の一例を示す。
FIG. 1 shows an example of a filtration tower used for filtration using the water treatment filter medium of the present invention.

第1図において、ろ過すべき水(原水)を流入管1の一
方から導入し、フランジ2及びパツキン3で固定された
金網4により支持された本発明水処理用ろ材6を通して
上向流方式によりろ過する。
In FIG. 1, water to be filtered (raw water) is introduced from one side of an inflow pipe 1, and is passed through a filter medium 6 for water treatment of the present invention supported by a wire mesh 4 fixed with a flange 2 and a packing 3 in an upward flow manner. Filter.

ろ過された水(処理水)は溢流管7より流出する。The filtered water (treated water) flows out from the overflow pipe 7.

ろ過は1〜3 kg lcr!程度の加圧下に120〜
300m/day程度の速度で行なうのが好ましい。
Filtration is 1-3 kg LCR! 120~ under pressure
It is preferable to carry out at a speed of about 300 m/day.

ろ過をしている間、圧力計接続管5に接続した圧力計に
よりろ過抵抗を測定し、ろ過抵抗が一定の値に達したと
きに原水を止め流入管1の他の一方から洗浄水を流入さ
せ1,5〜5kg/ffl程度の圧力で20〜90分程
度洗浄する。
During filtration, the filtration resistance is measured with a pressure gauge connected to the pressure gauge connection pipe 5, and when the filtration resistance reaches a certain value, the raw water is stopped and cleaning water is introduced from the other end of the inflow pipe 1. Wash at a pressure of about 1.5 to 5 kg/ffl for about 20 to 90 minutes.

本発明の水処理用ろ材は、一般の砂ろ過例えば下水処理
、産業排水処理、中水道システム等の緩速及び急速砕ろ
過装置に用いるのに好適であり、その場合に、従来のろ
過砂に比べてSS除去率が高くなる。
The water treatment filter medium of the present invention is suitable for use in general sand filtration devices, such as slow and rapid crushing filtration devices for sewage treatment, industrial wastewater treatment, gray water systems, etc. Compared to this, the SS removal rate is higher.

その際、前述した様に、上向流方式によった場合はSS
除去率が高くなるのみならず、ろ過抵抗が小さい、ろ過
サイクルが長い等の顕著な効果を奏する。
At that time, as mentioned above, if the upward flow method is used, the SS
Not only does it have a high removal rate, but it also has remarkable effects such as low filtration resistance and a long filtration cycle.

また、本発明の水処理用ろ材は安価でありコスト的にも
満足し得る。
Moreover, the water treatment filter medium of the present invention is inexpensive and can be satisfied in terms of cost.

本発明の水処理用ろ材が上記の如き優れたろ過性能を示
す理由は、廃水中のSSが、主として負に荷電している
ため、カチオン性ポリマーで被覆されて正に荷電した本
発明水処理用ろ材に対して静電気的に吸着されること、
及び該吸着がろ過層内で均一に起こることによると考え
られる。
The reason why the filter medium for water treatment of the present invention exhibits the excellent filtration performance as described above is that SS in wastewater is mainly negatively charged. to be electrostatically adsorbed to the filter media;
This is thought to be due to the fact that the adsorption occurs uniformly within the filtration layer.

以下、実施例及び比較例を挙げて、本発明を更に具体的
に説明する。
EXAMPLES Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.

実施例 1 攪拌機、温度計及び冷却器を取り付けた丸底フラスコに
水900重量部、アクリル酸エチル100重量部、2,
2′−アゾビス(アミノジブO/’?ン)塩酸塩50重
量部を入れ、窒素雰囲気下、70°Cで攪拌しながら、
4時間乳化重合し、カチオン性エマルジョンホリマーヲ
得り。
Example 1 900 parts by weight of water, 100 parts by weight of ethyl acrylate, 2,
Add 50 parts by weight of 2'-azobis(aminodibuO/'?n) hydrochloride, and while stirring at 70°C under a nitrogen atmosphere,
Emulsion polymerization was carried out for 4 hours to obtain a cationic emulsion polymer.

平均粒径0.8 ytw均等係数1.5のろ過砂5kg
と、粗粒砂として平均粒径2朋の砂1kgとを、リボン
ブレンダーに入れ、均一になる様子備混合後、攪拌下に
上記で得たカチオン性エマルジョンポリマーを、ポリマ
ー成分量として12gとなる量、噴霧添加し、均一にな
るまで混合して、その後、120℃で1時間加熱して水
を除去し、カチオン性ポリマーを被覆したろ過砂約6k
gを得た。
5 kg of filter sand with average particle size of 0.8 and ytw uniformity coefficient of 1.5
and 1 kg of sand with an average particle size of 2 mm as coarse sand are placed in a ribbon blender, and after mixing until uniform, add the cationic emulsion polymer obtained above while stirring to give a polymer component amount of 12 g. about 6k of filter sand coated with cationic polymer.
I got g.

これを処理砂Iとした。This was designated as treated sand I.

実施例 2 実施例1と同様に予備混合後の砂に市販のカチオン性エ
マルジョンポリマー(商品名:VONCOATSFC7
−50、大日本インキ化学■製)を、ポリマー成分量と
して12gとなる量、噴霧添加し、均一になるまで混合
した後、110℃で30分間加熱して水を除去し、カチ
オン性ポリマーを被覆したろ過砂約6ゆを得た。
Example 2 A commercially available cationic emulsion polymer (trade name: VONCOATSFC7) was added to the premixed sand in the same manner as in Example 1.
-50, manufactured by Dainippon Ink Chemical ■) was added by spraying in an amount to give a polymer component of 12 g, mixed until homogeneous, heated at 110°C for 30 minutes to remove water, and the cationic polymer Approximately 6 g of coated filter sand was obtained.

これを処理砂■とした。実施例 3 実施例1と同様に予備混合後の砂に、市販のカチオン性
ユリア樹脂水溶液(商標名ニューラミンP−1500、
三井東圧■製)を、ポリマー成分量として12gとなる
量、添加し、攪拌混合しながら、140℃で30分間加
熱して水を除去し、カチオン性ポリマーを被覆したろ過
砂約6kgを得た。
This was treated as treated sand ■. Example 3 A commercially available cationic urea resin aqueous solution (trade name Newlamin P-1500,
Mitsui Toatsu ■) was added in an amount to give a polymer component of 12 g, and while stirring and mixing, the mixture was heated at 140°C for 30 minutes to remove water, and about 6 kg of cationic polymer-coated filter sand was obtained. Ta.

これを処理砂■とした。比較例 1 比較として、平均粒径0.8 mm均等係数1.5のろ
過砂5kgと、平均粒径2mmの粗粒砂1kgとを、リ
ボンブレンダーで均一になる様に混合し、被覆処理して
いないろ過砂約6kgを得た。
This was treated as treated sand ■. Comparative Example 1 For comparison, 5 kg of filter sand with an average particle size of 0.8 mm and a uniformity coefficient of 1.5 and 1 kg of coarse grain sand with an average particle size of 2 mm were mixed uniformly using a ribbon blender and coated. Approximately 6 kg of unfiltered sand was obtained.

これを無処理砂とした。This was used as untreated sand.

実施例 4 処理砂1.n、III及び無処理砂を、第1図と同様の
ろ過塔(金網から溢流管までの高さ900mm、内径2
00mmのものを使用した)に充填高さ600mmで各
々充填し、下水処理場の2次処理廃水(SS濃度9.0
ppm)を、下部から上部へ流れる上向流方式により
、ろ過速度300 m/dayでろ過した。
Example 4 Treated sand 1. n, III and untreated sand in a filtration tower similar to that shown in Fig. 1 (height from wire mesh to overflow pipe: 900 mm, inner diameter: 2
00 mm) were filled to a filling height of 600 mm, and the secondary treated wastewater from a sewage treatment plant (SS concentration 9.0
ppm) was filtered at a filtration rate of 300 m/day using an upward flow method in which the flow flows from the bottom to the top.

ろ過開始時およびろ過開始から4時間経過後のろ過抵抗
を第1表に示す。
Table 1 shows the filtration resistance at the start of filtration and 4 hours after the start of filtration.

本実験においては、ろ過抵抗が2000imAqに達し
た時に、洗浄を行った。
In this experiment, cleaning was performed when the filtration resistance reached 2000 imAq.

第2表に洗浄を行うまでの時間、すなわちろ過サイクル
の時間を示す。
Table 2 shows the time until washing, ie, the time of the filtration cycle.

次に、下水処理場からの2次処理廃水(原水)として、
SS濃度が2.4ppm及び9.0ppmの2種類のも
のを、処理砂1,1.III及び無処理砂を充填した各
々のろ過塔に通した。
Next, as secondary treated wastewater (raw water) from the sewage treatment plant,
Two types of sand with SS concentrations of 2.4 ppm and 9.0 ppm were used as treated sand 1, 1. III and untreated sand.

原水及びろ過後の水(処理水)のSS濃度並びにSS除
去率(イ))を第3表に示す。
Table 3 shows the SS concentration and SS removal rate (a) of raw water and filtered water (treated water).

第1表、第2表及び第3表から明らかな様に、本発明水
処理用ろ材は、SS除去率が高い、ろ過抵抗が低い、及
びろ過サイクルが長いという優れたろ過性能を有するこ
とが判る。
As is clear from Tables 1, 2, and 3, the water treatment filter medium of the present invention has excellent filtration performance such as high SS removal rate, low filtration resistance, and long filtration cycle. I understand.

実施例 5 処理砂■及び無処理砂を実施例4で用いたろ過塔に各々
充填高さ600mmで充填し、下向流方式又は上向流方
式により、下水処理場の2次処理廃水(SS濃度20p
pm)をろ過速度300m/dayでろ過した。
Example 5 Treated sand ■ and untreated sand were filled into the filtration tower used in Example 4 to a filling height of 600 mm, and secondary treated wastewater (SS Concentration 20p
pm) was filtered at a filtration speed of 300 m/day.

ろ過開始時及びろ過開始から150分後のろ過抵抗並び
にろ過後の水のSS濃度を第4表に示す。
Table 4 shows the filtration resistance at the start of filtration and 150 minutes after the start of filtration, and the SS concentration of the water after filtration.

第4表から明らかな様に、本発明水処理用ろ材を下向流
方式で用いた場合、SS除去率は上向流方式よりもわず
かに高いが、ろ過抵抗は無処理砂より高く、結果として
ろ過サイクルが無処理砂より短くなる。
As is clear from Table 4, when the water treatment filter medium of the present invention is used in the downward flow method, the SS removal rate is slightly higher than in the upward flow method, but the filtration resistance is higher than that of untreated sand. As a result, the filtration cycle is shorter than that of untreated sand.

これに対し、上向流方式で用いた場合には、SS除去率
は下向流方式と同様に高く、かつろ過抵抗も無処理砂よ
り相当低くなり、結果としてろ過サイクルが長くなる。
On the other hand, when the upflow method is used, the SS removal rate is as high as the downflow method, and the filtration resistance is also considerably lower than that of untreated sand, resulting in a longer filtration cycle.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本発明水処理用ろ材を用いてろ過する場合に
使用するろ通塔の一例を示すものである。 図中の各記号は以下のものを示す。 1・・・・・・流入管、2・・・・・・フランジ、3・
・・・・・パツキン、4・・・・・・金網、5・・・・
・・圧力計接続管、6・・・・・・本発明水処理用ろ材
、7・・・・・・溢流管。
FIG. 1 shows an example of a filtration tower used in filtration using the water treatment filter medium of the present invention. Each symbol in the figure indicates the following. 1... Inflow pipe, 2... Flange, 3.
...Patzkin, 4...Wire mesh, 5...
... Pressure gauge connection pipe, 6 ... Filter medium for water treatment of the present invention, 7 ... Overflow pipe.

Claims (1)

【特許請求の範囲】 1 ろ過層をカチオン性ポリマーで被覆したことを特徴
とする水処理用ろ材。 2 カチオン性ポリマーの被覆量が、ろ過層100重量
部に対して、0.005〜10重量部である特許請求の
範囲第1項に記載の水処理用ろ材。 3 ろ過層をカチオン性ポリマーで被覆してなる水処理
用ろ材を用いて上向流式でろ過することを特徴とするろ
過方法。
[Scope of Claims] 1. A filter medium for water treatment, characterized in that a filtration layer is coated with a cationic polymer. 2. The water treatment filter medium according to claim 1, wherein the cationic polymer is coated in an amount of 0.005 to 10 parts by weight based on 100 parts by weight of the filtration layer. 3. A filtration method characterized by carrying out upward flow filtration using a water treatment filter material whose filtration layer is coated with a cationic polymer.
JP57118974A 1982-07-07 1982-07-07 Filter media and filtration methods for water treatment Expired JPS5940488B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57118974A JPS5940488B2 (en) 1982-07-07 1982-07-07 Filter media and filtration methods for water treatment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57118974A JPS5940488B2 (en) 1982-07-07 1982-07-07 Filter media and filtration methods for water treatment

Publications (2)

Publication Number Publication Date
JPS5910318A JPS5910318A (en) 1984-01-19
JPS5940488B2 true JPS5940488B2 (en) 1984-10-01

Family

ID=14749883

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57118974A Expired JPS5940488B2 (en) 1982-07-07 1982-07-07 Filter media and filtration methods for water treatment

Country Status (1)

Country Link
JP (1) JPS5940488B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6331538A (en) * 1986-07-25 1988-02-10 Kensetsusho Doboku Kenkyu Shocho Immobilizing carrier
JPS6331595A (en) * 1986-07-25 1988-02-10 Kensetsusho Doboku Kenkyu Shocho Treatment of activated sludge
EP0559525B2 (en) * 1992-02-28 2001-02-07 Tomoegawa Paper Co. Ltd. Thermal printing medium and method for preparing the same
JP2013027821A (en) * 2011-07-28 2013-02-07 Takuma Co Ltd Sand filtration device, and method for producing filter sand therefor

Also Published As

Publication number Publication date
JPS5910318A (en) 1984-01-19

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