JPS62168520A - Filtering method - Google Patents

Filtering method

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Publication number
JPS62168520A
JPS62168520A JP61006445A JP644586A JPS62168520A JP S62168520 A JPS62168520 A JP S62168520A JP 61006445 A JP61006445 A JP 61006445A JP 644586 A JP644586 A JP 644586A JP S62168520 A JPS62168520 A JP S62168520A
Authority
JP
Japan
Prior art keywords
exchange resin
aggregate
aggregates
shrinkage
powdered
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.)
Pending
Application number
JP61006445A
Other languages
Japanese (ja)
Inventor
Kiyomi Funabashi
清美 船橋
Masami Matsuda
将省 松田
Takashi Nishi
高志 西
Itaru Komori
小森 至
Hidekazu Miura
三浦 英一
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP61006445A priority Critical patent/JPS62168520A/en
Publication of JPS62168520A publication Critical patent/JPS62168520A/en
Pending legal-status Critical Current

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  • Treatment Of Water By Ion Exchange (AREA)
  • Filtration Of Liquid (AREA)

Abstract

PURPOSE:To reduce the generation of cracks in the powdery ion exchange resin bed formed on an element, by setting the shrinking degree of a powdery ion exchange resin aggregate due to the adsorption of a suspended substance to 0.8 or more. CONSTITUTION:In performing precoat filtering using an aggregate formed by mixing a powdery cation exchange resin and a powdery anion exchange resin as a filter aid, a value obtained by dividing the shrinking degree of the aggregate due to the adsorption of a suspended substance, that is, the volume of the aggregate having adsorbed the suspended substance by the volume of the aggregate adsorbing nothing is set to 0.8 or more. As a result, the shrinkage of the aggregate relating to the generation of cracks is prevented and the reliability of the powdery ion exchange resin at the time of filtering can be enhanced.

Description

【発明の詳細な説明】 〔発明の利用分野〕 本発明は、ろ過方法に係り、特に粉状イオン交換樹脂を
ろ過助剤とするろ過方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Application of the Invention] The present invention relates to a filtration method, and particularly to a filtration method using a powdered ion exchange resin as a filter aid.

〔発明の背景〕[Background of the invention]

高度な水処理用として、ろ過助剤を用いたろ過方法があ
る。この方法はナイロン製やステンレス製などのエレメ
ント上に粒径が10〜300μm程度の微細なろ過助剤
をプレコートし、プレコートしたろ過助剤上で水中の懸
濁物質を除去するものである。ろ過助剤として一般には
ケイソウ土やパルプセルロースなどが用いられているが
、原子力発電所など高度の水処理を必要とする場所では
通常のイオン交換樹脂(粒径約1+m程度)を破砕した
ものが用いられてきている。これは、特公昭47−44
903号公報によれば、約60〜400メツシユ(40
〜250μm)の陰イオン交換樹脂と陽イオン交換を一
定の比率で混合して用いられる。
For advanced water treatment, there is a filtration method using a filter aid. In this method, a fine filter aid with a particle size of about 10 to 300 μm is precoated on an element made of nylon or stainless steel, and suspended solids in water are removed on the precoated filter aid. Diatomaceous earth and pulp cellulose are generally used as filter aids, but in places where advanced water treatment is required, such as nuclear power plants, crushed ordinary ion exchange resins (approximately 1+ m particle size) are used as filter aids. It is being used. This is the special public service of 1977-44.
According to Publication No. 903, approximately 60 to 400 meshes (40
~250 μm) anion exchange resin and cation exchange resin are mixed at a certain ratio.

この粉状イオン交換樹脂には、その特質から通常のろ過
助剤と異なった特性が現われる。すなわち、陰イオン交
換樹脂と陽イオン交換樹脂は、そのイオン交換基のため
に、それぞれ正、負の相反する電荷をもち、これによっ
て、2つのイオン交換樹脂を混合すると、混合前の10
倍もの容積を持つ凝集体を形成する。またイオン交換基
によって形成された電荷は強いため、水中の懸濁物質の
除去性能も大きい特徴がある。さらには、母体がイオン
交換樹脂であるために、他のろ過助剤には全くみられな
い、イオンの除去性を有する。
Due to its characteristics, this powdered ion exchange resin exhibits characteristics different from those of ordinary filter aids. In other words, anion exchange resins and cation exchange resins have opposing charges, positive and negative, respectively, due to their ion exchange groups, and as a result, when two ion exchange resins are mixed, the 10
Forms aggregates with twice the volume. Furthermore, since the charge formed by the ion exchange group is strong, it has a great ability to remove suspended solids in water. Furthermore, since the base material is an ion exchange resin, it has ion removal properties that are not found in other filter aids.

しかしながら、粉状イオン交換樹脂が形成する凝集体が
水中の懸濁物質が吸着すると、その凝集体の容積が減少
し、エレメント上に形成された粉状イオン交換樹脂層に
無数のきれつが生ずる。これは、エレメントに通常公称
1μm程度と目開きの小さなナイロン系などの素材が用
いられているため、きれつ部分からの懸濁物質の漏洩は
ないが、エレメントのよごれのためにその交換頻度が増
大する。
However, when suspended substances in water are adsorbed to the aggregates formed by the powdered ion exchange resin, the volume of the aggregates decreases, and numerous cracks occur in the powdered ion exchange resin layer formed on the element. This is because the element is usually made of a material such as nylon with a nominal opening of about 1 μm, so there is no leakage of suspended solids from the cracked parts, but due to the element becoming dirty, it is difficult to replace it frequently. increase

このため、種々の対策が考えられ実行されている。その
一つは、ポリアクリル酸、ポリメタクリル酸、ポリアク
リル酸アミドやポリメタクリル酸アミドなどの高分子凝
集剤を添加し、凝集体の容積をある程度小さくしておき
、ろ過時のエレメント上で発生するきれつを少なくする
方法である。
For this reason, various countermeasures have been devised and implemented. One method is to add a polymer flocculant such as polyacrylic acid, polymethacrylic acid, polyacrylic acid amide, or polymethacrylic acid amide to reduce the volume of aggregates to a certain extent, which generates particles on the element during filtration. This is a method to reduce the amount of cracks that occur.

二つめは、長さが2mn程度の繊維を、粉状陽イオン交
換樹脂と粉状陰イオン交換樹脂混合時に添加し、これを
エレメント上にプレコートするもので、繊維によって凝
集体の収縮を少なくする方法である。三つめは、プレコ
ートを2段階で行・う方法である。これは、凝集体の収
縮によるきれつが生じる時点で、2回目のプレコートを
行い、ろ過によって発生したきれつをうづめてしまう方
法である。
The second method is to add fibers with a length of about 2 mm when mixing the powdered cation exchange resin and powdered anion exchange resin, and pre-coat this on the element, which reduces the shrinkage of the aggregates. It's a method. The third method is to perform precoating in two stages. In this method, when cracks occur due to shrinkage of the aggregates, a second precoating is performed to fill in the cracks caused by filtration.

これらの方法は、実機と同様な小型ろ過試験装置を用い
た実験結果では良好な結果が得られるが、実機では必ず
しも良好な結果が得られているとは限らない。
Although these methods yield good results in experiments using small filtration test equipment similar to the actual equipment, good results are not necessarily obtained in actual equipment.

このような事実から、実機との対応の良い、試験方法に
より、粉状イオン交換樹脂の使用条件を明確にすること
が望まれている。
Based on these facts, it is desired to clarify the usage conditions of powdered ion exchange resins using a test method that is compatible with actual equipment.

〔発明の目的〕[Purpose of the invention]

本発明の目的は、上記従来技術の欠点をなくする、すな
わち、きれつ発生の少ない粉状イオン交換樹脂凝集体の
調製条件を提供することにある。
An object of the present invention is to eliminate the drawbacks of the prior art described above, that is, to provide conditions for preparing powdery ion exchange resin aggregates with less cracking.

〔発明の概要〕[Summary of the invention]

本発明の特徴は、粉状陽イオン交換樹脂と粉状陰イオン
交換樹脂を混合して生成した凝集体容積と、懸濁物質を
吸着させた凝集体容積を、ろ過状態を考慮して一方向よ
り圧力を加えながら測定し、測定した後者の凝集体容積
を前者の凝集体容積で除した値が0.7 以上となるよ
うに凝集体を調製することにある。
The feature of the present invention is that the volume of aggregates generated by mixing powdered cation exchange resin and powdered anion exchange resin and the volume of aggregates on which suspended substances are adsorbed are unidirectionally adjusted in consideration of the filtration state. The objective is to prepare aggregates such that the measured volume of the latter aggregate divided by the volume of the former aggregate becomes 0.7 or more by measuring while applying more pressure.

〔発明の実施例〕[Embodiments of the invention]

本発明は、粉状陽イオン交換樹脂と粉状陰イオン交換樹
脂の凝集体の収縮と、きれつの発生の原因とを評価した
結果に基づいてなされたものである。
The present invention was made based on the results of evaluating the shrinkage of aggregates of powdered cation exchange resins and powdered anion exchange resins and the causes of cracking.

以下、その結果の詳細を述べる。第2図に、凝集体の収
縮と、きれつ発生原因を模式的に示す。
The details of the results will be described below. FIG. 2 schematically shows the shrinkage of aggregates and the causes of cracking.

凝集体の収縮発生原因は、懸濁物質の吸着と、ろ過時の
差力上昇によるものの2つである。前者は懸濁物質がエ
レメント上の凝集体の表面はど多く除去されるため、凝
集体表面の収積が大きく、凝集体内面はど小さくなり、
結果としてきれつが生じる。−右後者は、ろ過時の差圧
上昇によるものであるが、初期差圧0.1 kg/d以
下から、最終差圧は1〜5 kg/cJと変化するため
、凝集体の収縮が大きくなる。第3図に差圧と凝集体の
収縮の関係を示す。この図かられかるように、差圧が小
さい部分で急激に収縮し、その後、ゆるやかに収縮する
。その収縮は、初期の凝集体の容積の−〜一と大きい。
There are two causes for shrinkage of aggregates: adsorption of suspended substances and increase in differential force during filtration. In the former case, a large amount of suspended matter is removed from the surface of the aggregate on the element, so the collection on the surface of the aggregate is large, and the inner surface of the aggregate becomes smaller.
Cracks occur as a result. - The latter case on the right is due to an increase in differential pressure during filtration, but since the initial differential pressure is 0.1 kg/d or less, the final differential pressure changes from 1 to 5 kg/cJ, so the shrinkage of the aggregates is large. Become. Figure 3 shows the relationship between differential pressure and contraction of the aggregate. As can be seen from this figure, there is a rapid contraction in the area where the differential pressure is small, and then a gradual contraction. The shrinkage is -~1 of the initial aggregate volume.

しかしながら、この差圧による収縮は、エレメント上の
凝集体層で均一に発生するため、前者の懸濁物質の吸着
による収縮と異なり、きれつは発生しない。したがって
、凝集体の収縮ときれつの発生とを関連づけるためには
、まず、差圧による収縮を排除し、懸濁物質の吸着によ
る収縮のみを評価する必要がある。
However, since the contraction due to this differential pressure occurs uniformly in the aggregate layer on the element, unlike the former contraction due to adsorption of suspended matter, no cracking occurs. Therefore, in order to correlate the shrinkage of aggregates with the occurrence of cracks, it is first necessary to eliminate shrinkage due to differential pressure and evaluate only shrinkage due to adsorption of suspended solids.

以下、図面を用いて、懸濁物質の吸着による凝集体の収
縮量の測定方法を述べる。第3図に測定装置の一例を示
す。第1図において、1は凝集体、2はシリンダー、3
はピストン、4は重り、5は目皿である。まず、第1図
の装置を用いて、懸濁物質を吸着していない状態で凝集
体の容積を測定する。この手順としては、最初に水中で
粉状陽イオン交換樹脂と粉状陰イオン交換樹脂を混合し
凝集体を調製する。この時の粉状陽イオン交換樹脂と粉
状陰イオン交換樹脂の混合比は実機の使用条件に合わせ
る。水の量は、粉状イオン交換樹脂量1g当り20mQ
以上となるようにする。次いて、調製した凝集体を水と
共にシリンダ2内に入れる。
Hereinafter, a method for measuring the amount of shrinkage of aggregates due to adsorption of suspended matter will be described using drawings. FIG. 3 shows an example of a measuring device. In Figure 1, 1 is an aggregate, 2 is a cylinder, and 3
is a piston, 4 is a weight, and 5 is a perforated plate. First, using the apparatus shown in FIG. 1, the volume of the aggregate is measured without adsorbing suspended matter. In this procedure, first, a powdered cation exchange resin and a powdered anion exchange resin are mixed in water to prepare an aggregate. At this time, the mixing ratio of the powdered cation exchange resin and powdered anion exchange resin is adjusted to the usage conditions of the actual machine. The amount of water is 20mQ per 1g of powdered ion exchange resin.
Make sure that the above is achieved. The prepared aggregate is then placed into the cylinder 2 together with water.

余剰の水は目皿5を通り排出される。次いで、ピストン
3を挿入し目的の圧力が加わるように重り4をピストン
3の上にのせる。このまま、ピストン3の動きが止まる
まで待った後、凝集体の容積をピストン3の移動距離と
シリンダ2の内径から算出する。
Excess water passes through the perforated plate 5 and is discharged. Next, the piston 3 is inserted and a weight 4 is placed on the piston 3 so that the desired pressure is applied. After waiting until the movement of the piston 3 stops, the volume of the aggregate is calculated from the moving distance of the piston 3 and the inner diameter of the cylinder 2.

次に懸濁物質を吸着した凝集体の容積を測定する。この
場合は、水中で凝集体を形成された後懸濁物質を添加し
凝集体に吸着させる。懸濁物質の量は、凝集体の吸着量
以上に加える。過剰な懸濁物質は、凝集体の水中での沈
降速度が懸濁物質よりも大きいので、デカンテーション
によって分離する。このようにして調製した懸濁物質吸
着の凝集体の容積を、懸濁物質を吸着していない凝集体
と同様の方法で測定する。この時の圧力は両者とも同一
条件とする。
Next, the volume of the aggregates adsorbing the suspended matter is measured. In this case, after aggregates are formed in water, suspended substances are added and adsorbed onto the aggregates. The amount of suspended solids is added in excess of the adsorbed amount of the aggregates. Excess suspended solids are separated by decantation since the sedimentation rate of aggregates in water is greater than that of suspended solids. The volume of the suspended solids-adsorbed aggregates thus prepared is measured in the same manner as for the aggregates that do not adsorb suspended solids. The pressure at this time is the same for both.

このようにして測定した凝集体容積から、懸濁物質吸着
による凝集体の収縮度を評価する。収縮度は、懸濁物質
を吸着した凝集体容積を、なにも吸着していない凝集体
容積で除して求める。
The degree of shrinkage of the aggregate due to adsorption of suspended matter is evaluated from the aggregate volume thus measured. The degree of shrinkage is determined by dividing the volume of aggregates that have adsorbed suspended matter by the volume of aggregates that have not adsorbed anything.

以上のようにして凝集体の収縮度と、ろ適時の懸濁物質
透過率との関係を調べた。その結果を第1−図に示す。
As described above, the relationship between the degree of shrinkage of aggregates and the permeability of suspended solids at the appropriate time of filtration was investigated. The results are shown in Figure 1.

ここでは、粉状陽イオン交換樹脂と粉状陰イオン交換樹
統を2:1の割合で、高分子凝集剤は1 m g / 
g樹脂を加えて混合し凝集体を形成した。懸濁物質とし
ては、原子力発電所復水ろ過脱塩器を考慮し、粒径約1
−μmのFezO8を用いた。
Here, powdered cation exchange resin and powdered anion exchange tree were used at a ratio of 2:1, and the polymer flocculant was used at 1 mg/g/g.
g resin was added and mixed to form aggregates. Considering the condensate filtration and desalination equipment of nuclear power plants, the suspended solids have a particle size of approximately 1.
-μm FezO8 was used.

また、収縮度の測定圧力は、きれつの発生が多い0.5
 kg/、nとした。その結果、収縮度0.8以上でF
ezOδ透過率も低下した。これは、第2図で説明した
ようにきれつが発生しないためである。
In addition, the measurement pressure for the degree of shrinkage is 0.5, which causes many cracks.
kg/, n. As a result, F
The ezOδ transmittance also decreased. This is because cracking does not occur as explained in FIG. 2.

本発明を具体的に実施するには種々の方法がある。以下
、本発明を実施しうるに好適な実施例を述べる。
There are various ways to specifically implement the present invention. Hereinafter, preferred embodiments for carrying out the present invention will be described.

実施例1 通常の粉状イオン交換樹脂は平均粒径が約40μmであ
るが、粒径を変えることによって収縮度を変化させるこ
とができる。第5図にその結果を示す。平均粒径が50
μm以上となると収縮度は0.8 以上となり、Fez
O8の透過率は低下し、良好なろ過が行えることがわか
る。また、平均粒径が大きくなるに従って、FexOδ
透過率が再び増加するが、これは粒径が大きくなるに従
って、粒状イオン交換樹脂の単位重量当りの表面積も低
下したFaxOaの捕捉力が低下するためである。
Example 1 A normal powdered ion exchange resin has an average particle size of about 40 μm, but the degree of shrinkage can be changed by changing the particle size. Figure 5 shows the results. Average particle size is 50
When it is more than μm, the degree of shrinkage is more than 0.8, and Fez
It can be seen that the O8 transmittance decreases, indicating that good filtration can be performed. Moreover, as the average particle size increases, FexOδ
The transmittance increases again, but this is because as the particle size increases, the surface area per unit weight of the particulate ion exchange resin also decreases, and the trapping power of FaxOa decreases.

したがって、粒径によって粉状イオン交換樹脂凝集体の
収縮度を0.8 以上とするためには、Fez○δ透過
率の点から粉状イオン交換樹脂の平均粒径は50〜15
0μmが好適である。
Therefore, in order to make the shrinkage degree of the powdery ion exchange resin aggregate 0.8 or more depending on the particle size, the average particle size of the powdery ion exchange resin should be 50 to 15 from the viewpoint of Fez○δ transmittance.
0 μm is suitable.

実施例2 通常の粉状イオン交換樹脂では高分子凝集剤の添加量は
1 m g / g樹脂であるが、これを増加させるこ
とによって、収縮度を大きく、すなわち懸濁物質の吸着
による凝集体の収縮を少なくすることもできる。第6図
に高分子凝集剤の添加量と凝集体の収縮度を示す。高分
子凝集剤の添加量が10mg/g樹脂以上で収縮度0.
8 以上となる。
Example 2 For ordinary powdered ion exchange resins, the amount of polymer flocculant added is 1 mg/g resin, but by increasing this, the degree of shrinkage is increased, that is, the amount of aggregates due to adsorption of suspended substances is increased. It is also possible to reduce the shrinkage of FIG. 6 shows the amount of polymer flocculant added and the degree of shrinkage of the aggregate. When the amount of polymer flocculant added is 10 mg/g resin or more, the degree of shrinkage is 0.
8 or more.

したがって、粉状イオン交換樹脂凝集体の収縮度を0.
8以上とするためには、高分子凝集剤の添加量をLon
g/g樹脂以上にすればよい。
Therefore, the degree of shrinkage of the powdered ion exchange resin aggregate is set to 0.
In order to make it 8 or more, the amount of polymer flocculant added should be Lon
g/g resin or more.

実施例3 粉状イオン交換樹脂の粉状陽イオン交換樹脂と粉状陰イ
オン交換樹脂とを1=1.または2:1゜で通常混合さ
れるが、この混合割合を変更することで凝集体の収縮度
を変えることができる。第7図に粉状イオン交換樹脂の
混合割合と凝集体の収縮度の関係を示す。第7図の横軸
は粉状陽イオン交換樹脂と粉状陰イオン交換樹脂の全粉
状イオン交換樹脂重量に対する粉状陽イオン交換樹脂重
量の割合を示した。ちなみに、従来の混合割合である粉
状陽イオン交換樹脂:粉状陰イオン交換樹脂が2=1の
場合、第7図横軸は0.66 となり、1:1の場合は
第7図横軸は0.5 となる。この図かられかるように
、本発明の目的とする凝集体収縮度を0.8 以上にす
るには、粉状陽イオン交換樹脂重量を全粉状イオン交換
樹脂重量0.2 以下または0.8 以上とすればよい
Example 3 Powdered cation exchange resin and powdered anion exchange resin of powdered ion exchange resin were mixed in a ratio of 1=1. Alternatively, they are usually mixed at a ratio of 2:1°, but by changing this mixing ratio, the degree of shrinkage of the aggregate can be changed. FIG. 7 shows the relationship between the mixing ratio of the powdered ion exchange resin and the degree of shrinkage of the aggregate. The horizontal axis of FIG. 7 shows the ratio of the powdered cation exchange resin weight to the total powdered ion exchange resin weight of the powdered cation exchange resin and the powdered anion exchange resin. By the way, when the conventional mixing ratio of powdered cation exchange resin and powdered anion exchange resin is 2=1, the horizontal axis in Figure 7 is 0.66, and when it is 1:1, the horizontal axis in Figure 7 is 0.66. becomes 0.5. As can be seen from this figure, in order to achieve the aggregate shrinkage degree of 0.8 or more, which is the objective of the present invention, the weight of the powdered cation exchange resin should be reduced to 0.2 or less by the total weight of the powdered ion exchange resin. It may be 8 or more.

実施例4 実施例1,2.3では、それぞれ粉状イオン交換樹脂の
粒径、高分子凝集剤の添加量、粉状陽イオン交換樹脂と
粉状陰イオン交換樹脂の混合割合の条件のみを変えた場
合の例を示したが、これらの2つ以上を組合せても、同
様の効果を奏する。
Example 4 In Examples 1 and 2.3, only the particle size of the powdered ion exchange resin, the amount of polymer flocculant added, and the mixing ratio of the powdered cation exchange resin and powdered anion exchange resin were set. Although an example is shown in which the values are changed, the same effect can be obtained even if two or more of these are combined.

また、これらの組合せによって、凝集体の収縮度を0.
9以上にすれば、さらにきれつ防止の信頼性を向上でき
る。
Moreover, by these combinations, the shrinkage degree of the aggregate can be reduced to 0.
If the value is 9 or more, the reliability of crack prevention can be further improved.

上記実施例1〜4によれば、きれつ発生の有無°を事前
に知り、それを防止できる。したがって、本方法は、製
造段階における品質管理、および、使用直前の性能確認
に利用できる。
According to Examples 1 to 4 above, it is possible to know in advance whether or not cracking will occur and to prevent it. Therefore, this method can be used for quality control at the manufacturing stage and performance confirmation immediately before use.

〔発明の効果〕〔Effect of the invention〕

本発明によれば、きれつの発生に関係する凝集体の収縮
を防止し、粉状イオン交換樹脂のろ適時の信頼性向上が
できる。
According to the present invention, it is possible to prevent the shrinkage of aggregates related to the occurrence of cracking, and improve the reliability of filtering powdered ion exchange resin in a timely manner.

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

第1図は本発明における粉状イオン交換樹脂のFezO
a吸着による収縮とろ過性能との関係を示した線図、第
2図は、収縮原因ときれつの関係を示した説明図、第3
図は本発明の一実施例の凝集体の収縮度を測定するため
の装置の断面図、第4図は差圧による凝集体の収縮を示
した線図、第5図は粉状イオン交換樹脂の粒径と凝集体
の収縮度を示した線図、第6図は高分子凝集剤添加量と
凝集体数縮度の関係を示した線図、第7図は粉状陽イオ
ン交換樹脂と粉状陰イオン交換樹脂の混合比と収縮度の
関係を示した線図である。 2・・・シリンダー、3・・・ピストン、4・・・重り
、5・・・目皿。
Figure 1 shows the powdery ion exchange resin FezO in the present invention.
a Diagram showing the relationship between shrinkage due to adsorption and filtration performance, Figure 2 is an explanatory diagram showing the relationship between shrinkage causes and cracking, and Figure 3
The figure is a cross-sectional view of an apparatus for measuring the shrinkage degree of aggregates according to an embodiment of the present invention, Figure 4 is a diagram showing the shrinkage of aggregates due to differential pressure, and Figure 5 is a powdered ion exchange resin. Figure 6 is a diagram showing the relationship between the particle size of the polymer flocculant and the shrinkage degree of the aggregates, Figure 7 is a diagram showing the relationship between the amount of polymer flocculant added and the shrinkage degree of the aggregate number FIG. 2 is a diagram showing the relationship between the mixing ratio of powdered anion exchange resin and the degree of shrinkage. 2... Cylinder, 3... Piston, 4... Weight, 5... Perforated plate.

Claims (1)

【特許請求の範囲】[Claims] 1、粉状陽イオン交換樹脂と粉状陰イオン交換樹脂を混
合した凝集体をろ過助剤とするプレコートろ過において
、当該凝集体の一方向より加圧した条件で測定した容積
で、処理対象の廃水中の懸濁物質を吸着させた当該凝集
体の一方向より加圧した条件で測定した容積を、除した
値が0.8以上となるように凝集体を調製することを特
徴とするろ過方法。
1. In pre-coat filtration using aggregates of a mixture of powdered cation exchange resin and powdered anion exchange resin as a filter aid, the volume measured under the condition of applying pressure from one direction of the aggregates is the volume of the target object to be treated. Filtration characterized by preparing aggregates such that the volume obtained by dividing the volume of the aggregates adsorbing suspended substances in wastewater under conditions of pressurization from one direction is 0.8 or more. Method.
JP61006445A 1986-01-17 1986-01-17 Filtering method Pending JPS62168520A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61006445A JPS62168520A (en) 1986-01-17 1986-01-17 Filtering method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61006445A JPS62168520A (en) 1986-01-17 1986-01-17 Filtering method

Publications (1)

Publication Number Publication Date
JPS62168520A true JPS62168520A (en) 1987-07-24

Family

ID=11638607

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61006445A Pending JPS62168520A (en) 1986-01-17 1986-01-17 Filtering method

Country Status (1)

Country Link
JP (1) JPS62168520A (en)

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