JPS6014610B2 - Pre-coating method for powdered ion exchange resin - Google Patents
Pre-coating method for powdered ion exchange resinInfo
- Publication number
- JPS6014610B2 JPS6014610B2 JP54149148A JP14914879A JPS6014610B2 JP S6014610 B2 JPS6014610 B2 JP S6014610B2 JP 54149148 A JP54149148 A JP 54149148A JP 14914879 A JP14914879 A JP 14914879A JP S6014610 B2 JPS6014610 B2 JP S6014610B2
- Authority
- JP
- Japan
- Prior art keywords
- ion exchange
- exchange resin
- resin
- precoating
- precoat
- 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
- 239000003456 ion exchange resin Substances 0.000 title claims description 28
- 229920003303 ion-exchange polymer Polymers 0.000 title claims description 28
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 title claims description 26
- 238000000576 coating method Methods 0.000 title claims description 11
- 239000011347 resin Substances 0.000 claims description 39
- 229920005989 resin Polymers 0.000 claims description 39
- 239000002002 slurry Substances 0.000 claims description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 19
- 239000011248 coating agent Substances 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims 3
- 230000002776 aggregation Effects 0.000 description 8
- 238000005054 agglomeration Methods 0.000 description 7
- 239000003957 anion exchange resin Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 229920000867 polyelectrolyte Polymers 0.000 description 4
- 238000001914 filtration Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000002440 industrial waste Substances 0.000 description 2
- 230000000968 intestinal effect Effects 0.000 description 2
- 210000000936 intestine Anatomy 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003758 nuclear fuel Substances 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Treatment Of Water By Ion Exchange (AREA)
- Filtration Of Liquid (AREA)
Description
【発明の詳細な説明】
本発明は原子炉一次冷却水、原子炉給水のための復水、
核燃料プール水、産業廃棄物処理系設備における低電導
度廃液、他の産業廃液、例えば火力発電復水、などの水
又は廃水の浄化処理に用いる渡過器又は脱塩器のプレコ
ート剤保持体に粉末イオン交換樹脂をプレコートする方
法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention provides primary reactor cooling water, condensate water for reactor feed water,
For pre-coat agent holding bodies in transitors or desalters used for purifying water or wastewater such as nuclear fuel pool water, low conductivity waste liquids from industrial waste treatment equipment, and other industrial waste liquids, such as thermal power generation condensate. This invention relates to a method for precoating powdered ion exchange resin.
ここに粉末イオン交換樹脂とは粒蓬約5〜250仏の粒
状イオン交換樹脂又はこの粒隆範囲に粉砕されたイオン
交換樹脂をいう。従来粉末イオン交換樹脂をプレコート
剤として保持体上にプレコートするため脇イオン交モ劇
樹脂と陰イオン交換樹脂とを十分に混合した水性スラリ
ーを渡過器又は脱塩器に導くことによりプレコーテイン
グが行なわれてきた。The term "powdered ion exchange resin" as used herein refers to a granular ion exchange resin having a particle diameter of about 5 to 250 grains, or an ion exchange resin pulverized into this range. Conventionally, in order to pre-coat the holder using a powdered ion exchange resin as a pre-coating agent, pre-coating is carried out by introducing an aqueous slurry in which an ion exchange resin and an anion exchange resin are thoroughly mixed into a transfer vessel or a desalter. It has been done.
しかし陽・陰両イオン交f剣睦脂を清浄な水中で混合縄
拝すると樹脂が相互に集合して団塊化するためプレコー
テイングが困難であった。このような樹脂の過度の団塊
化を制御し樹脂のプレコーティングを可能にする方法と
して特公昭40−16325号公報にはポリアクリル酸
メチルのような水落性樹脂質ポリ電解質を樹脂混合物に
添加することを含む方法が記載されている。However, when positive and negative ion exchange resins are mixed in clean water, the resins aggregate together and form nodules, making pre-coating difficult. As a method for controlling such excessive agglomeration of the resin and enabling pre-coating of the resin, Japanese Patent Publication No. 16325/1987 discloses adding a water-dropable resinous polyelectrolyte such as polymethyl acrylate to the resin mixture. A method including this is described.
しかしこの方法では電解質の添加及び添加後の粉末樹脂
の団塊化が所要範囲内にあることを確認する操作が必要
であるなどの欠点を有している。即ちこの方法は電解質
を満塁添加して静電気量を中和し、凝集力を弱めるので
一見合理的に考えられるが、劣化し易い不安定な電解質
の管理、調整、添加後の効果の程度を確認するため、調
整の都度スラリーをサンプリングしなければならず、運
転管理上、操作上非常にわずらわしい欠点をもっている
。However, this method has drawbacks such as the addition of the electrolyte and the necessity of operations to confirm that the agglomeration of the powdered resin after addition is within the required range. In other words, this method seems reasonable at first glance as it neutralizes the amount of static electricity and weakens the cohesive force by adding a full base of electrolyte, but it is necessary to manage and adjust unstable electrolytes that are prone to deterioration, and confirm the extent of the effect after addition. Therefore, it is necessary to sample the slurry each time adjustment is made, which has the disadvantage of being extremely troublesome in terms of operation management and operation.
又性能面を取上げると添加する塁がほかではあるとはい
え有害な電解質を加えるため、イオン交換性能、水中け
ん濁物の吸着除去についても好ましくない要因が増加す
る。本発明はプレコート式猿過器又は脱塩器のプレコー
ティングに関する前記欠陥を排除し、水溶性樹脂質ポリ
電解質を添加することなく簡単な方法で粉末陽・陰イオ
ン交換樹脂の団塊化の過度の進行を防ぎ良好なプレコー
ト層を保持体上に形成させる方法を提供することを目的
として、その方法は櫨過器又は脱塩器に供V給するプレ
コート層を形成させる樹脂水性スラリーの濃度を一定範
囲に制御することにより行なわれる。In addition, in terms of performance, the added base adds a harmful electrolyte, which increases unfavorable factors in terms of ion exchange performance and adsorption and removal of suspended matter in water. The present invention eliminates the above-mentioned deficiencies regarding pre-coating of pre-coated sieves or demineralizers and eliminates excessive agglomeration of powdered cation-anion exchange resins in a simple manner without adding water-soluble resinous polyelectrolytes. The purpose of this method is to provide a method for forming a good precoat layer on a holder by preventing the progress of the precoat layer, and the method involves keeping the concentration of the resin aqueous slurry forming the precoat layer fed to the filter or desalter at a constant concentration. This is done by controlling the range.
すなわち樹脂スラリーを特定の低濃度で渡過器に供給す
ることによって、樹脂粒子の衝突回数を少なくし、静電
気作用による凝集力を弱め、従来用いられている水溶性
樹脂質ポリ電解質を添加することなしに過大な団塊化作
用を抑制するものである。In other words, by supplying the resin slurry at a specific low concentration to the transfer vessel, the number of collisions of resin particles is reduced, the cohesive force due to electrostatic action is weakened, and the conventionally used water-soluble resin polyelectrolyte is added. This is to suppress the excessive baby-booming effect.
0.01重量%より稀薄な場合には凝集作用が低下する
ため団塊化が過度に抑制され、プレコート層はよりち密
になりすぎ通水抵抗が大となり好ましくない。When it is diluted less than 0.01% by weight, the agglomeration effect is reduced, so that agglomeration is excessively suppressed, and the precoat layer becomes too dense, resulting in high water flow resistance, which is not preferable.
又プレコートの所要時間も長くなる欠点を有する。逆に
樹脂スラリー濃度が0.0亀重量%をこえると凝集作用
が増大し団塊化が促進し、プレコート層の均一性が失わ
れる。It also has the disadvantage that the time required for precoating is long. On the other hand, if the resin slurry concentration exceeds 0.0% by weight, the aggregation effect will increase, agglomeration will be promoted, and the uniformity of the precoat layer will be lost.
従来法で行なわれているプレコート濃度は通常1重量%
程度である。The precoating concentration used in conventional methods is usually 1% by weight.
That's about it.
本発明によればプレコート式櫨過器又は脱塩器に供給す
る樹脂水性スラリ−の濃度は0.01〜0.06重量%
に制御される。According to the present invention, the concentration of the resin aqueous slurry supplied to the precoat filter or desalter is 0.01 to 0.06% by weight.
controlled by.
本発明の一実施態様では樹脂をレジンフィードタンク内
で水と混合して水性スラリーに形成し、そのスラリ−を
ェゼクタにより吸引稀釈し、次に循環水に混合稀釈する
ことにより所定濃度範囲の樹脂水性スラリーを形成させ
る。この場合レジンフイードタンク中で約8重量%のス
ラリーを形成させ、ヱゼクタで約4%に稀釈し穣後に循
環水で稀釈して0.01〜0.0亀重量%のスラリ−に
するのが好ましい。均一良好なプレコ−ト層を形成させ
るため、通常レジンフイードタンク中に所定量の純水を
入れ健イオン交換樹脂を入れて約10分縄拝し、次に腸
イオン交換樹脂を入れ水量を調整した後約20分損拝す
る。In one embodiment of the present invention, resin is mixed with water in a resin feed tank to form an aqueous slurry, the slurry is suction diluted by an ejector, and then mixed and diluted with circulating water to obtain a resin in a predetermined concentration range. Form an aqueous slurry. In this case, a slurry of about 8% by weight is formed in a resin feed tank, diluted to about 4% in an ejector, and then diluted with circulating water to make a slurry of 0.01 to 0.0% by weight. is preferred. In order to form a uniform and good pre-coat layer, usually put a specified amount of pure water into a resin feed tank, add healthy ion exchange resin, and boil for about 10 minutes, then add intestinal ion exchange resin and reduce the amount of water. After adjusting, I bowed for about 20 minutes.
雛梓又は放置時間を長くすると樹脂の団塊化が鈍る懐向
があり縄梓又は蝿洋放置時間を5〜4鞘時間にすること
が好ましい。しかしそれ以上長時間櫨梓又は放置しても
効果に差異を生じない。プレコーティングは3〜7.3
仇/h・猿過面積の線流速で行なうのが好ましく、また
プレコーテイングを2〜1′畑時間の時間行なうのが好
ましい。It is preferable to leave the rope or pods for 5 to 4 hours because the longer the time for leaving the chicks or the pods, the slower the agglomeration of the resin will be. However, there is no difference in effectiveness even if it is left in place for a longer period of time. Pre-coating is 3-7.3
It is preferable to carry out the process at a linear flow rate of 200 m/h/300 m area, and it is preferable to carry out the precoating for a time of 2 to 1' field time.
以下図面を参照して実施例について説明する。第1図に
おいて、レジンフィードタンク8に適量の純水を張り縄
杵機9を起動する。鷹梓機9は回転数を0〜25仇pm
の間任意に調節できるもので十分な蝿梓力を有するもの
を用いる。陰イオン交換樹脂を投入し十分燈拝した後腸
イオン交換樹脂を投入し純水を加えて樹脂濃度を調整し
た後さらに約20分間十分に縄拝する。陰・陽両イオン
交f剣樹脂の混合割合は腸イオン交モ剣樹脂/陰イオン
交換樹脂=1〜3/1であり、総重量は約lk9・乾燥
樹脂/〆・櫨過面積である。イオン交壬灘樹脂の混合割
合は上記割合に限定されず本発明の浄化システムを設置
する場所の水質条件により決定されるものである。Examples will be described below with reference to the drawings. In FIG. 1, an appropriate amount of pure water is poured into the resin feed tank 8 and the rope punch machine 9 is started. The Takaazusa machine 9 has a rotation speed of 0 to 25 pm.
Use a device that can be adjusted arbitrarily between the two and has sufficient strength. After adding the anion exchange resin and allowing sufficient lighting, the intestine ion exchange resin was added, pure water was added to adjust the resin concentration, and the intestine was further heated for approximately 20 minutes. The mixing ratio of both negative and positive ion exchange resins is intestinal ion exchange resin/anion exchange resin = 1 to 3/1, and the total weight is about lk 9. dry resin/〆. The mixing ratio of the ion exchange resin is not limited to the above ratio, but is determined depending on the water quality conditions at the location where the purification system of the present invention is installed.
レジンフィードタンク8内の樹脂スラリーの濃度は約8
%とした。The concentration of the resin slurry in the resin feed tank 8 is approximately 8
%.
この濃度はできるだけ高濃度にする方が容器を小型に製
作できるので好ましいが健投混合及びスラリー抜出し‘
こ問題を生じ高濃度では均一蝿拝が良好でなくスラリー
の定量的抜出し及び移送が困難となるのでスラリーの性
状とプロセス上の配慮によって決定される。プレコート
式猿過器又は脱榎器として第1図の櫓1を用いる。槽1
は下部に原水入口、上部に猿過水出口、中間内部にプレ
コート剤保持体3を備えその下方に分散板2を有する堅
型の装置で樹脂のドレン機構(図面では省略)を備えて
いる。糟1及びプレコートタンク4には予め必要量の純
水を満たしプレコートポンプ5を起動し弁17を徐々に
開き流量計7を見ながら源過流速を約37の′h・櫨過
面積として恒遠循環を行なった後弁16を開いてェゼク
タ11の駆動水12を流量計13により調節しスラリー
弁15を開く。プレコートボンプ5の入口部への樹脂ス
ラリ−濃度14はェゼクタ駆動水12とスラリー弁15
とにより任意に調節できる。It is preferable to make this concentration as high as possible because the container can be made smaller;
This problem occurs when the concentration is high, and uniform dispersion is not good, making quantitative extraction and transfer of the slurry difficult, so it is determined by the properties of the slurry and consideration in the process. The turret 1 shown in FIG. 1 is used as a pre-coat type sieve or decoat device. Tank 1
The device is a rigid device having a raw water inlet at the bottom, a filtration water outlet at the top, a precoat agent holder 3 in the middle, and a dispersion plate 2 below it, and is equipped with a resin drain mechanism (not shown in the drawings). Pre-fill the required amount of pure water in the tank 1 and the pre-coat tank 4, start the pre-coat pump 5, gradually open the valve 17, and while watching the flow meter 7, set the source overflow velocity to about 37'h and the overflow area. After the circulation, the valve 16 is opened, the driving water 12 of the ejector 11 is adjusted by the flow meter 13, and the slurry valve 15 is opened. The resin slurry concentration 14 to the inlet of the precoat pump 5 is controlled by the ejector driving water 12 and the slurry valve 15.
It can be adjusted as desired.
本実施例ではこの樹脂スラリー濃度は約4%以下にし循
環水で下記濃度に稀釈して渡過櫓に供V給した。プレコ
ート進行状況はしベルゲージ10で照査できる。In this example, the resin slurry concentration was kept at about 4% or less, and the resin slurry was diluted with circulating water to the following concentration and supplied to the transit tower. Pre-coat progress can be checked using the bell gauge 10.
プレコート剤保持体3は図2に示す如く支持臭20,2
1により槽内に支持されている金網18で構成され糟1
に供V給された増薄樹脂スラリー中の樹脂は金網18上
に保持され樹脂プレコート層19を形成する。所定のプ
レコート層が形成された後ェゼクタ駆動水12を止めス
ラリー弁15を閉じる。なおこのようにプレコートした
櫨過器による原水の浄化は通常、その後プレコート保持
を行ない最低1仇/h・猿過面積の循環流量を保持しな
がら採水弁を開き未処理水を通しプレコート剤保持ポン
プを停止し適宜の深水簿過速度で裸水することにより行
なわれる。As shown in FIG.
1 consists of a wire mesh 18 that is supported in the tank by 1
The resin in the thinned resin slurry supplied to the V is held on the wire mesh 18 to form a resin precoat layer 19. After a predetermined precoat layer is formed, the ejector driving water 12 is stopped and the slurry valve 15 is closed. In addition, when purifying raw water using a pre-coated filtration device, the pre-coat is then maintained, and the water intake valve is opened while maintaining a circulation flow rate of at least 1 k/h/saru area and the untreated water is passed through to retain the pre-coat agent. This is done by stopping the pump and draining the water at an appropriate depth and overspeed.
上記のようにプレコート樹脂スラリーの濃度を変えて行
なったときのプレコート状態は次の如くであった。The precoating conditions were as follows when the concentration of the precoating resin slurry was changed as described above.
観察は目視外観による(糟は透明アクリル製)櫨過流速
こ3.7の′h・櫨過面積○:プレコート良好:プレコ
ート層表面が平らで均一×:プレコート不良:プレコー
ト層表面の凹凸が著しく均一とならない。Observation is based on visual appearance (the cassette is made of transparent acrylic) Flow rate is 3.7'h, area of filtration is ○: Good precoat: The surface of the precoat layer is flat and uniform ×: Poor precoat: The surface of the precoat layer is noticeably uneven. It will not be uniform.
△:プレコートやや良:プレコート層表面に凹凸を生ず
る場合もある。Δ: Precoat somewhat good: Irregularities may occur on the surface of the precoat layer.
従ってプレコートスラリー濃度は通常0.04%で最大
0.06%まで許容される。Therefore, the precoat slurry concentration is normally 0.04% and a maximum of 0.06% is allowed.
本発明の方法によればプレコート式猿過器のプレコーテ
ィングにおいて水落性樹脂質ポリ電解質のようなプレコ
ート調整剤を必要としないのでそれに関連する操作が不
要となり運転操作が簡単になる。According to the method of the present invention, a precoating conditioner such as a water-repellent resinous polyelectrolyte is not required in the precoating of the precoat type sieve, so that the related operations are not necessary and the operation becomes simple.
さらに本発明の方法ではプレコート剤スラリーが一定濃
度で猿過槽に供給されるのでプレコート量を任意に調節
することができる。Furthermore, in the method of the present invention, since the precoat agent slurry is supplied to the sieving tank at a constant concentration, the amount of precoat can be adjusted as desired.
従釆の方法ではプレコートタンクに必要なブレコート剤
を投入してスラリーを調製しその全量をプレコートタン
ク−櫨過器−プレコートタンクの循環ラインを用いてプ
レコートするのでプレコーテイングの進行とと&こプレ
コートタンク内の樹脂スラリー濃度が変化するので途中
で中止することができないが、本発明の方法によればレ
ジンフィードタンクに任意回数に必要な樹脂を投入して
スラリーを形成させ各回の所要プレコート量をレベルゲ
ージで確認することができ、また複数の櫨過槽に対して
必要なプレコート剤をレジンフィードタンクに投入し、
各渡過槽に対応するプレコート槽をレジンフィードタン
クのレベルゲージで確認することにより連続的にプレコ
ートすることができる。In the conventional method, the necessary brecoat agent is put into a precoat tank to prepare a slurry, and the entire amount is precoated using a circulation line from the precoat tank to the filter to the precoat tank. Since the resin slurry concentration in the tank changes, it cannot be stopped midway, but according to the method of the present invention, the necessary amount of resin is added to the resin feed tank any number of times to form a slurry, and the required amount of precoat for each time is determined. It can be checked with a level gauge, and the necessary pre-coating agent for multiple filter tanks can be added to the resin feed tank.
Continuous precoating can be performed by checking the precoating tank corresponding to each transition tank using the level gauge of the resin feed tank.
第1図は本発明の実施例のフロ−シート、第2図はプレ
コート剤支持部説明図である。
1…・・・糟、3・・・・・・プレコート剤保持体、4
・・・・・・プレコートタンク、8……レジンフイード
タンク、10……レベルゲージ、11……エゼクタ。
第1図第2図FIG. 1 is a flow sheet of an embodiment of the present invention, and FIG. 2 is an explanatory diagram of a precoat agent support portion. 1...Cast, 3...Precoat agent holder, 4
...Pre-coat tank, 8...Resin feed tank, 10...Level gauge, 11...Ejector. Figure 1 Figure 2
Claims (1)
レコート剤保持体に粉末イオン交換樹脂をプレコートす
る方法において、水と粒径約5〜250μmの粉末イオ
ン交換樹脂とによって、粉末イオン交換樹脂を0.01
〜0.06重量%を含む水性スラリーに調製し、該水性
スラリーを前記プレコート式濾過器又はプレコート式脱
塩器へ供給してプレコートを行うことを特徴とする粉末
イオン交換樹脂のプレコーテイング方法。 2 プレコート式濾過器又はプレコート式脱塩器のプレ
コート剤保持体に粉末イオン交換樹脂をプレコートする
方法において、水と粒径約5〜250μmの粉末イオン
交換樹脂とをレジンフイードタンク内で混合し高濃度ス
ラリーを調製し、粉末イオン交換樹脂の該高濃度スラリ
ーを該レジンフイードタンクから水エゼクタで吸引して
、プレコート循環水に混合せしめ、この混合された水性
スラリー中の粉末イオン交換樹脂の濃度を0.01〜0
.06重量%として前記プレコート式濾過器又はプレコ
ート式脱塩器へ供給してプレコートを行うことを特徴と
する粉末イオン交換樹脂のプレコーテイング方法。 3 プレコート式濾過器又はプレコート式脱塩器のプレ
コート剤保持体に粉末イオン交換樹脂をプレコートする
方法において、水と粒径約5〜250μmの粉末イオン
交換樹脂とによって、粉末イオン交換樹脂を0.01〜
0.06重量%含む水性スラリーに調整し、前記プレコ
ート式濾過器又はプレコート式脱塩器の濾過面に対し3
〜7.3m/hの線流速となるよう前記水性スラリーを
供給しプレコートすることを特徴とする粉末イオン交換
樹脂のプレコーテイング方法。[Claims] 1. A method for precoating a powdered ion exchange resin on a precoating agent holder of a precoating type filter or a precoating type demineralizer, using water and a powdered ion exchange resin having a particle size of about 5 to 250 μm, 0.01 powdered ion exchange resin
A method for precoating a powdered ion exchange resin, which comprises preparing an aqueous slurry containing 0.06% by weight, and supplying the aqueous slurry to the precoating type filter or precoating type demineralizer for precoating. 2. In a method of precoating a powdered ion exchange resin on a precoat agent holder of a precoat type filter or a precoat type demineralizer, water and a powdered ion exchange resin with a particle size of about 5 to 250 μm are mixed in a resin feed tank. A highly concentrated slurry of powdered ion exchange resin is prepared, and the highly concentrated slurry of powdered ion exchange resin is sucked from the resin feed tank by a water ejector and mixed with the precoat circulating water, and the powdered ion exchange resin in the mixed aqueous slurry is Concentration from 0.01 to 0
.. A method for pre-coating a powdered ion exchange resin, characterized in that pre-coating is performed by supplying the resin to the pre-coating type filter or pre-coating type demineralizer as 0.6% by weight. 3. In a method of precoating a powder ion exchange resin on a precoat agent holding body of a precoat type filter or a precoat type demineralizer, the powder ion exchange resin is coated with water and a powder ion exchange resin having a particle size of about 5 to 250 μm. 01~
The aqueous slurry was adjusted to contain 0.06% by weight, and
A method for pre-coating a powdered ion exchange resin, characterized in that the aqueous slurry is supplied and pre-coated at a linear flow rate of ~7.3 m/h.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54149148A JPS6014610B2 (en) | 1979-11-17 | 1979-11-17 | Pre-coating method for powdered ion exchange resin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54149148A JPS6014610B2 (en) | 1979-11-17 | 1979-11-17 | Pre-coating method for powdered ion exchange resin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5673546A JPS5673546A (en) | 1981-06-18 |
| JPS6014610B2 true JPS6014610B2 (en) | 1985-04-15 |
Family
ID=15468817
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP54149148A Expired JPS6014610B2 (en) | 1979-11-17 | 1979-11-17 | Pre-coating method for powdered ion exchange resin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6014610B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2550097B1 (en) * | 1983-08-03 | 1988-08-05 | Duolite International Sa | PACKING PROCESS FOR PRE-LAYERED FILTERS FOR PURIFYING FLUIDS |
| WO2004033765A1 (en) * | 2002-10-08 | 2004-04-22 | Ebara Corporation | Electrode for electrolytic processing |
-
1979
- 1979-11-17 JP JP54149148A patent/JPS6014610B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5673546A (en) | 1981-06-18 |
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