JPH1147629A - Method for evaluating separation performance of suspended solids - Google Patents
Method for evaluating separation performance of suspended solidsInfo
- Publication number
- JPH1147629A JPH1147629A JP20431097A JP20431097A JPH1147629A JP H1147629 A JPH1147629 A JP H1147629A JP 20431097 A JP20431097 A JP 20431097A JP 20431097 A JP20431097 A JP 20431097A JP H1147629 A JPH1147629 A JP H1147629A
- Authority
- JP
- Japan
- Prior art keywords
- evaluating
- particles
- suspended
- performance
- separation performance
- 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
Links
Landscapes
- Separation Of Solids By Using Liquids Or Pneumatic Power (AREA)
Abstract
(57)【要約】
【課題】懸濁物質の分離性能を評価するにあたり、高粒
径粒子による影響を受けずに、低粒径粒子の分離性能を
評価する懸濁物質の分離性能評価方法を提供する。
【解決手段】懸濁物質の分離性能を評価するにあたり、
平均粒子径が1μm以上5μm以下の懸濁粒子を使用す
ることを特徴とする懸濁物質の分離性能評価方法。
(57) [Summary] [PROBLEMS] To evaluate the separation performance of suspended solids, which evaluates the separation performance of low-particles without being affected by high-particles, in evaluating the separation performance of suspended solids. provide. In evaluating the separation performance of a suspended substance,
A method for evaluating the performance of separating suspended substances, wherein suspended particles having an average particle diameter of 1 μm or more and 5 μm or less are used.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、平均粒子径が1〜
10μmの粒子の除去を目的とするろ過手段の性能評価
において、粒子径が1〜5μmの範囲にある粒子を懸濁
物質に用いることで、ろ過手段の特性を明確に把握しな
がら評価を行う懸濁物質の分離性能評価方法に関するも
のである。TECHNICAL FIELD The present invention relates to the present invention, wherein the average particle size is from 1 to 1.
In the performance evaluation of filtration means for the purpose of removing particles of 10 μm, by using particles having a particle diameter in the range of 1 to 5 μm as a suspended substance, evaluation is performed while clearly grasping the characteristics of the filtration means. The present invention relates to a method for evaluating the performance of separating suspended substances.
【0002】[0002]
【従来の技術】水中浮遊物質をろ過するためのろ材とし
て、平、綾、朱子のいわゆる3元織組織を基本とする格
子構造の織物が広く使用されている。特公昭62−13
046号公報や特公平2−47244号公報には、緯糸
に極細繊維を用いた織物を起毛加工し、表面に極細繊維
の立毛を形成したろ過布が知られている。また、表面に
繊維束を有するろ材として、実公平5−34730号公
報、実開平4−14112号公報、特願平6−3047
05に記載されたフィルターやろ過布が知られている。2. Description of the Related Art A woven fabric having a lattice structure based on a so-called ternary weave of flat, twill, and satin is widely used as a filter medium for filtering suspended substances in water. Tokiko Sho 62-13
Japanese Patent Publication No. 046 and Japanese Patent Publication No. 2-47244 disclose a filter cloth obtained by raising a woven fabric using ultrafine fibers for the weft and forming nap of the ultrafine fibers on the surface. Further, as a filter medium having a fiber bundle on the surface, Japanese Utility Model Publication No. Hei 5-34730, Japanese Utility Model Publication No. Hei 4-14112, and Japanese Patent Application No. 6-3047.
The filter and the filter cloth described in No. 05 are known.
【0003】これらのろ過布によって河川水や地下水の
浄化を行うにあたっては、原水中に含まれる比較的大き
な粒子がろ過布表面に捕捉・吸着され、目詰まりした状
態となるために、運転開始初期に処理水量が低減する傾
向がある。つまり、いわばプレフィルターのようなもの
がろ過布表面に形成されるため、ろ過布本来の性能が発
現されにくいといった問題があった。ろ過布を用いて、
逆に比較的懸濁物質濃度が低くかつ粒子径も低い水泳用
プール水や入浴用水の浄化を行う際には、プレフィルタ
ー状の層が形成されにくいため懸濁物質除去性が低下す
る傾向が見られる。このように、対象とする原水の性状
によってろ過性能に差異が見られるため、標準評価原水
によるろ過布の性能把握が不可避であるが、これまでの
標準評価原水は適切な粒子径分布を有する懸濁物質が見
出されていなかったため、高粒径粒子による影響を受け
る傾向があった。In purifying river water and groundwater with these filter cloths, relatively large particles contained in raw water are caught and adsorbed on the surface of the filter cloth and become clogged. Tends to reduce the amount of treated water. In other words, since what is called a pre-filter is formed on the surface of the filter cloth, there is a problem that the original performance of the filter cloth is hardly exhibited. Using a filter cloth,
Conversely, when purifying swimming pool water or bathing water, which has a relatively low concentration of suspended solids and a small particle size, the removal of suspended solids tends to be reduced due to the difficulty of forming a pre-filter-like layer. Can be seen. As described above, since there is a difference in the filtration performance depending on the properties of the target raw water, it is inevitable to grasp the performance of the filter cloth using the standard evaluation raw water, but the standard evaluation raw water so far has an appropriate particle size distribution. Since no turbid matter was found, it tended to be affected by the large particle size.
【0004】[0004]
【本発明が解決しようとする課題】本発明は、懸濁物質
の分離性能を評価するにあたり、高粒径粒子による影響
を受けずに、低粒径粒子の分離性能を評価する懸濁物質
の分離性能評価方法を提供することを課題としている。SUMMARY OF THE INVENTION The present invention relates to a method for evaluating the separation performance of suspended particles, which is not influenced by high-particles, and evaluates the separation performance of low-particles. It is an object to provide a method for evaluating separation performance.
【0005】[0005]
【課題を解決するための手段】本発明者らは上記の事情
に鑑み、種々の検討を重ねた結果、以下の方法で課題が
解決できることを見出した。すなわち、懸濁物質の分離
性能を評価するにあたり、平均粒子径が1μm以上5μ
m以下の懸濁粒子を使用することによって、ろ過手段の
正確な性能が評価できることを見出した。Means for Solving the Problems In view of the above circumstances, the present inventors have made various studies, and as a result, have found that the problem can be solved by the following method. That is, in evaluating the separation performance of a suspended substance, the average particle diameter is 1 μm or more and 5 μm or more.
It has been found that by using suspended particles of m or less, the accurate performance of the filtration means can be evaluated.
【0006】さらに、懸濁粒子としてはカオリンなどの
微細鉱物あるいは硫酸ヒドラジンとヘキサメチレンテト
ラミンから調整するホルマジンが最適であることを見出
した。Furthermore, it has been found that fine minerals such as kaolin or formazine prepared from hydrazine sulfate and hexamethylenetetramine are most suitable as suspended particles.
【0007】すなわち、本発明は、ろ過手段を用いて水
中の懸濁物質の分離性能を評価するにあたり、平均粒子
径が1μm以上5μm以下の懸濁粒子を使用することを
特徴とする懸濁物質の分離性能評価方法である。That is, according to the present invention, in evaluating the performance of separating suspended substances in water using a filtration means, suspended particles having an average particle diameter of 1 μm to 5 μm are used. Is a method for evaluating separation performance.
【0008】[0008]
【発明の実施の形態】以下、本発明について具体的に説
明する。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described specifically.
【0009】本発明に使用されるろ過手段としては布帛
からなるろ過布、さらにはろ過層が0.1〜10μmの
極細繊維よりなるろ過布を用いることが好ましい。この
ようなろ過布としては、緯糸に極細繊維を用いた織物を
起毛加工し、表面に極細繊維の立毛を形成したろ過布
や、さらに好ましくは表面に繊維束を有するろ過布が挙
げられる。表面に繊維束を有するろ過布としては、例え
ば、織物からなるベース層に極細繊維束の一端もしくは
一部が根元部としてベース層に一体化されたろ過布が挙
げられる。極細繊維束とベース層との一体化の方法とし
ては、接着剤による接着、熱融着、超音波接着、ベース
層の糸と繊維束との交絡およびこれらの組み合わせなど
が挙げられるがこれらに限定されるものではない。[0009] As the filtering means used in the present invention, it is preferable to use a filtering cloth made of cloth, and furthermore, a filtering cloth made of ultrafine fibers having a filtering layer of 0.1 to 10 µm. Examples of such a filter cloth include a filter cloth obtained by raising a woven fabric using microfibers for the weft and forming nap of the microfibers on the surface, and more preferably a filter cloth having a fiber bundle on the surface. Examples of the filter cloth having a fiber bundle on the surface include a filter cloth in which one end or a part of an ultrafine fiber bundle is integrated with a base layer made of a woven fabric as a root. Examples of the method of integrating the microfine fiber bundle with the base layer include, but are not limited to, bonding with an adhesive, heat fusion, ultrasonic bonding, entanglement of the yarn and fiber bundle of the base layer, and a combination thereof. It is not something to be done.
【0010】本発明において、ろ過層を構成する極細繊
維に使用しうる繊維は、繊維形成能を有する高分子物質
からなり、ナイロン6、ナイロン66、ナイロン12、
共重合ナイロンなどのポリアミド、芳香族ポリアミド、
ポリエチレンテレフタレート、共重合ポリブチレンテレ
フタレートなどのポリエステル、全芳香族ポリエステ
ル、ポリエチレ、ポリプロピレンなどのポリオレフィ
ン、ポリウレタン、ポリアクリロニトリル、ポリ塩化ビ
ニル、ポリビニルアルコール、ビニル重合体、ポリ塩化
ビニリデン、ポリハイドロサルファイト、ポリフッ化エ
チレン、共重合ポリフッ化エチレン、ポリオキシメチレ
ンなどが挙げられる。また、これらの高分子物質を複数
組み合わせた芯鞘構造、多重芯鞘構造、海島構造、バイ
メタル構造などの複合繊維や、繊維の種類の組み合わせ
にも目的に応じて用いられる。繊維の太さとしては、比
較的細い10μm以下がより好ましいが、微粒子の細く
性能を向上させるには0.1〜9μmがより好ましく、
繊維の耐久性を高く維持しつつ微粒子の細く性能を向上
させるには、1〜8μmがさらに好ましい。In the present invention, the fibers that can be used for the ultrafine fibers constituting the filtration layer are composed of a polymer substance having a fiber forming ability, and include nylon 6, nylon 66, nylon 12,
Polyamides such as copolymerized nylon, aromatic polyamides,
Polyesters such as polyethylene terephthalate and copolymerized polybutylene terephthalate, polyolefins such as wholly aromatic polyesters, polyethylene and polypropylene, polyurethane, polyacrylonitrile, polyvinyl chloride, polyvinyl alcohol, vinyl polymers, polyvinylidene chloride, polyhydrosulfite, and polyolefin Ethylene fluoride, copolymerized polyfluoroethylene, polyoxymethylene and the like. Further, composite fibers having a core-sheath structure, a multi-core-sheath structure, a sea-island structure, a bimetal structure, or the like in which a plurality of these polymer substances are combined, and combinations of fiber types are also used according to the purpose. The thickness of the fiber is more preferably 10 μm or less, which is relatively thin, and more preferably 0.1 to 9 μm to improve the performance of the fine particles.
In order to improve the fineness of the fine particles while maintaining high durability of the fiber, the thickness is more preferably 1 to 8 μm.
【0011】本発明においてろ過手段の分離性能を評価
するための懸濁物質としては、平均粒子径が1〜5μm
の微粒子を使用することが好ましい。このような微粒子
としては、岩石由来の微細鉱物や、シリカ、アルミナ、
酸化鉄、ケイソウ土などの無機系微粒子、活性炭、カー
ボンブラックやホルマジンなどの有機系微粒子が挙げら
れる。In the present invention, the suspended substance for evaluating the separation performance of the filtration means has an average particle diameter of 1 to 5 μm.
It is preferable to use fine particles of the above. Such fine particles include fine minerals derived from rock, silica, alumina,
Examples include inorganic fine particles such as iron oxide and diatomaceous earth, and organic fine particles such as activated carbon, carbon black and formazine.
【0012】岩石由来の微細鉱物としては、例えばカオ
リナイト、デツカイト、ナクライト、ハロイサイト、そ
の他のカンダイト群の微細な粘土、モンモリロナイト、
フラー土、ベントナイト、サポナイトその他のスメクタ
イト群の微細な粘土、タルク、マイカおよびこれら粘土
の実質的な割合を占める鉱物残滓が挙げられる。無機系
微粒子としては、シリカ、アルミナ、硫酸バリウム、炭
酸カルシウム、水酸化アルミニウムなどが挙げられる。
有機系微粒子としては、活性炭やカーボンブラック、ラ
テックス粒子、ホルマジンなどが挙げられる。中でもホ
ルマジンを使用するのが特に好適な方法である。ホルマ
ジンはヘキサメチレンテトラミンおよび硫酸ヒドラジニ
ウムより調整されるものであるが、水中での分散性、安
定性が良く、水の濁度を測定する場合の校正標準液とし
て、特に欧米で使用されている。ホルマジンは水中での
粒径が重量分布で1〜5μm(コールターマルチサイザ
ー(コールター社製)による測定)と特にシャープであ
るので、極細繊維を用いたろ過布の低粒径性能評価に特
に適していることを見出している。The rock-derived fine minerals include, for example, kaolinite, decittite, nacrite, halloysite, other fine clay of the kandite group, montmorillonite,
Fuller's earth, bentonite, saponite and other fine clays of the smectite group, talc, mica and mineral residues which make up a substantial proportion of these clays are mentioned. Examples of the inorganic fine particles include silica, alumina, barium sulfate, calcium carbonate, and aluminum hydroxide.
Examples of the organic fine particles include activated carbon, carbon black, latex particles, and formazin. Among them, use of formazine is a particularly preferred method. Formazin is prepared from hexamethylenetetramine and hydrazinium sulfate, but has good dispersibility and stability in water, and is particularly used in Europe and the United States as a calibration standard solution for measuring turbidity of water. Formazin has a particularly sharp particle size in water of 1 to 5 μm in weight distribution (measured by a Coulter Multisizer (manufactured by Coulter)), and is particularly suitable for evaluating the low particle size performance of a filter cloth using ultrafine fibers. Are finding that.
【0013】以下に実施例を用いて本発明をより具体的
に説明するが、これに限定されるものではない。Hereinafter, the present invention will be described more specifically with reference to Examples, but it should not be construed that the invention is limited thereto.
【0014】[0014]
(実施例1)ベース層の糸(F1)として、ポリエチレ
ンテレフタレートからなる250デニール、48フィラ
メントの糸を経糸および緯糸に用いて織物を構成し、ろ
過層の繊維束(F2)としてポリエチレンテレフタレー
トからなる240デニール、576フィラメントの糸に
仮撚加工を行って、27%の捲縮率を有する仮撚加工糸
を用いた。経糸F1の本数に対して一定の割合でF2を
配置して、上下2枚の同じ織物からなる2重織物を作成
した。この織物は一定間隔をおいて離れた上下2枚の織
物の間をF2が往復を繰り返して構成された2重織物で
ある。F2は上と下の織物の緯糸と交互に交絡点をもっ
て両者を一体化しているものである。(Example 1) A fabric is formed by using a 250 denier, 48 filament yarn of polyethylene terephthalate as a warp and a weft as a yarn (F1) of a base layer, and a polyethylene terephthalate as a fiber bundle (F2) of a filtration layer. False twisting was performed on a yarn of 240 denier and 576 filaments, and a false twisted yarn having a crimp rate of 27% was used. By arranging F2 at a fixed ratio with respect to the number of warp yarns F1, a double woven fabric composed of two upper and lower same woven fabrics was prepared. This woven fabric is a double woven fabric in which F2 repeats reciprocating between two upper and lower woven fabrics separated by a predetermined interval. F2 is one in which the wefts of the upper and lower fabrics are integrated alternately with the entanglement points.
【0015】得られた一体化2重織物について、厚さ方
向の指定した位置で織物の表面と平行にF2の繊維束を
スライスすることにより、ろ過層の表面がF2の繊維束
の自由端となった織物を得た。このときのF2の繊維束
の長さは8.0mmであった。次にこれらの織物を回転
しているブラシロールとバックロールの間に通して、繊
維束が自然にやや傾斜している方向に合わせて繊維束を
ブラッシングして開繊させ、ろ過層の表面に繊維をくま
なく展開させると同時に繊維の方向を揃えた。引き続
き、開繊した繊維束の面を加熱した金属ロールの表面に
張力をかけて押し当てて、繊維束をセットしてろ過布を
つくった。こうして得られたろ過布について、ろ過性能
を評価した。なお評価はろ過前後のSS粒子数の変化か
ら算出した阻止率(今後、数平均阻止率と呼ぶ)および
ろ過前後のSS重量変化から算出した阻止率(重量平均
阻止率と呼ぶ)で行った。ここでSSとは、懸濁物質
(Suspended Solids)の略で、一般的に1μmカットの
ろ紙でろ過し、ろ紙に残る成分のことである。In the obtained integrated double fabric, the fiber bundle of F2 is sliced in parallel with the surface of the fabric at a designated position in the thickness direction, so that the surface of the filter layer is in contact with the free end of the fiber bundle of F2. Woven fabric. At this time, the length of the fiber bundle of F2 was 8.0 mm. Next, pass these fabrics between the rotating brush roll and back roll, brush the fiber bundles in the direction where the fiber bundles are naturally slightly inclined, and open the fibers. The fibers were spread all over, and at the same time, the directions of the fibers were aligned. Subsequently, the surface of the opened fiber bundle was pressed against the surface of the heated metal roll with tension, and the fiber bundle was set to produce a filter cloth. The filtration performance of the filter cloth thus obtained was evaluated. The evaluation was performed based on the rejection calculated from the change in the number of SS particles before and after filtration (hereinafter referred to as a number average rejection) and the rejection calculated from the change in SS weight before and after filtration (referred to as the weight average rejection). Here, SS is an abbreviation of suspended solids (Suspended Solids), and is generally a component that is filtered through a 1 μm-cut filter paper and remains on the filter paper.
【0016】数平均阻止率は、ろ過前後の原水およびろ
過水それぞれの単位容積中に存在する粒子数をコールタ
ーマルチサイザー(コールター社製)で計測し、下記式
から算出した。また重量阻止率は、JIS工場排水試験
方法、JIS−K0102を参考にして測定した。The number average rejection was calculated from the following equation by measuring the number of particles present in a unit volume of each of raw water and filtered water before and after filtration using a Coulter Multisizer (manufactured by Coulter). The weight inhibition rate was measured with reference to JIS factory drainage test method, JIS-K0102.
【0017】すなわち、図1に示した通り、上部ろ過器
1と下部ろ過台4との間にろ過布2を取り付け、金属製
クランプ6で固定した後、吸引瓶7側から減圧して常に
250mmH2 Oの圧力差がある状態で原水をろ過して
ろ過液を得た。このろ過液と原水をそれぞれミリポアA
P1μmカットろ紙(日本ミリポア製)でろ過し、絶乾
重量を測定して次式から算出した。That is, as shown in FIG. 1, a filter cloth 2 is attached between the upper filter 1 and the lower filter table 4, and is fixed with a metal clamp 6, and then the pressure is reduced from the suction bottle 7 side to 250 mmH. The raw water was filtered with a pressure difference of 2 O to obtain a filtrate. Millipore A
The solution was filtered through a P1 μm cut filter paper (manufactured by Nippon Millipore), the absolute dry weight was measured, and calculated from the following equation.
【0018】 各粒径ごとの数平均阻止率(%)=1−(A/B)×100 …(1) ただし、A:ろ過水中に含まれる粒子数 B:原水中に含まれる粒子数 重量平均阻止率(%) =1−{(b′−a′)/(b−a)}×100 …(2) ただし、a :原水をろ過する前のろ紙重量(g) a′:ろ過水をろ過する前のろ紙重量(g) b :原水の残留物を含んだろ紙重量(g) b′:ろ過水の残留物を含んだろ紙重量(g) また、評価原水中の標準物質の平均粒子径はコールター
マルチサイザー(コールター社製)によって測定した。Number average rejection (%) for each particle size = 1− (A / B) × 100 (1) where A: number of particles contained in filtered water B: number of particles contained in raw water Weight Average rejection (%) = 1-{(b′-a ′) / (ba)} × 100 (2) where a: filter paper weight before filtering raw water (g) a ′: filtered water Filter paper weight before filtration (g) b: Paper weight containing residues of raw water (g) b ': Paper weight containing residues of filtered water (g) Also, average of standard substances in the raw water for evaluation The particle size was measured using a Coulter Multisizer (manufactured by Coulter Inc.).
【0019】評価原水は次の手順で調整した。Evaluation raw water was prepared in the following procedure.
【0020】ホルマジン液の一般的な調整方法である、
ASTM(1984) D(1889-81 Standard Test Methods
for TURBIDUTY OF WATER "1984Annual Book of ASTMSta
ndards", Vol 11.01, 268-274,ASTM,Philadelphia )や
JIS K 0101(工業用水試験方法、13-18 )に
記載の方法に準じた。すなわち硫酸ヒドラジン1.00
0gをメスフラスコに採り、精製水を加えて全量を10
0mlとしA液とした。別にヘキサメチレンテトラミン
10.00gをメスフラスコ100mlに採り、精製水
を加えて全量を100mlとし、これをB液とした。次
にA液5ml、B液5mlずつをメスフラスコ100m
lに採って混合し、25±3℃で24時間放置した後、
精製水を加えて全量を100mlとし、ホルマジン原液
とした。この原液を精製水で20倍に希釈して、約10
mg/lの原水を調整した。This is a general method for preparing a formazin solution.
ASTM (1984) D (1889-81 Standard Test Methods
for TURBIDUTY OF WATER "1984 Annual Book of ASTMSta
ndards ", Vol 11.01, 268-274, ASTM, Philadelphia) and JIS K 0101 (Industrial water test method, 13-18), that is, hydrazine sulfate 1.00.
0 g is placed in a volumetric flask, and purified water is added to make a total amount of 10 g.
0 ml was used as solution A. Separately, 10.00 g of hexamethylenetetramine was placed in a 100 ml volumetric flask, and purified water was added to make the total amount 100 ml. Next, 5 ml each of solution A and 5 ml each of solution B were added to a measuring flask 100 m.
After mixing at 25 ± 3 ° C. for 24 hours,
Purified water was added to make a total volume of 100 ml, which was used as a formazin stock solution. This stock solution was diluted 20-fold with purified water to obtain about 10
mg / l of raw water was prepared.
【0021】表1にホルマジン原水の平均粒径および濁
度を、表2に重量平均阻止率およびろ過布によるろ過後
の処理水の濁度を、図2にホルマジン粒子の各粒径にお
ける数平均阻止率を示した。Table 1 shows the average particle diameter and turbidity of raw formazine water, Table 2 shows the weight average rejection and the turbidity of the treated water after filtration with a filter cloth, and FIG. 2 shows the number average of each particle diameter of formazin particles. The rejection rate was shown.
【0022】(実施例2)実施例1で作成したろ過布を
用い、次の原水のろ過性能を評価した。(Example 2) The filtration performance of the following raw water was evaluated using the filter cloth prepared in Example 1.
【0023】カオリン10.0g,ピロリン酸ナトリウ
ム10水和物0.2gを精製水1.5lと共に、ホモミ
キサーで正確に5分間4000rpmで攪拌し、更に精
製水を加えて10lとしたものをカオリン原液とした。
この原液は約1000mg/lであり、100倍に希釈
して10mg/l原水とした。10.0 g of kaolin and 0.2 g of sodium pyrophosphate decahydrate were stirred with 1.5 l of purified water for exactly 5 minutes at 4000 rpm using a homomixer, and further purified water was added to make 10 l. The stock solution was used.
This stock solution was about 1000 mg / l, and was diluted 100 times to obtain 10 mg / l stock water.
【0024】表1にこの原水の性状を、表2にこの原水
によるろ過布のろ過性能評価結果を、図2に数平均阻止
率を示した。Table 1 shows the properties of the raw water, Table 2 shows the results of evaluating the filtration performance of the filter cloth using the raw water, and FIG. 2 shows the number average rejection.
【0025】(比較例1)実施例1で作成したろ過布を
用い、次の原水のろ過性能を評価した。(Comparative Example 1) The filtration performance of the following raw water was evaluated using the filter cloth prepared in Example 1.
【0026】ケイソウ土(ラヂオライト#100(昭和
化学工業製)を2Lビーカに10g採取し、精製水1.
5lを加えて正確に5分間4000rpmで攪拌し、さ
らに精製水を加えて合計10lとした。この液を10L
下口瓶に移して10分間放置して高粒径粒子を沈殿さ
せ、底部から5cm以上の上澄み液を取り出して標準原
液とした。この標準原液を精製水で希釈して3mg/l
原水とした。この原水の性状およびろ過布のろ過性能を
表2、図2に示した。10 g of diatomaceous earth (Radiolite # 100 (manufactured by Showa Kagaku Kogyo) is collected in a 2 L beaker, and purified water 1.
5 l was added and stirred at 4000 rpm for exactly 5 minutes, and purified water was further added to make a total of 10 l. 10 L of this solution
The particles were transferred to a lower bottle and allowed to stand for 10 minutes to precipitate high-particle-size particles, and a supernatant liquid of 5 cm or more was taken out from the bottom and used as a standard stock solution. This standard stock solution was diluted with purified water to give 3 mg / l
Raw water. The properties of the raw water and the filtration performance of the filter cloth are shown in Table 2 and FIG.
【0027】重量平均阻止率は、ホルマジンを用いた場
合もケイソウ土を標準物質とした場合とほぼ同様の値を
示す。しかし、各粒径ごとの阻止率(数平均阻止率)に
着目すると、ホルマジンを標準物質として用いた原水で
ろ過布を評価した場合に、最も低粒径範囲における阻止
率が高いことが分かる。本現象の詳細なところは不明で
あるが、ホルマジンは粒径分布が比較的狭いために、1
0μm以下の粒子の阻止性を把握する際に、他の標準物
質よりも粒径ごとの阻止率がクリアーに評価できる結果
となった。高粒径粒子の影響が少ないことも、寄与して
いると考えられる。The weight-average rejection shows almost the same value when formazin is used as when diatomaceous earth is used as a standard substance. However, focusing on the rejection (number-average rejection) for each particle size, it can be seen that the rejection in the lowest particle size range is highest when the filter cloth is evaluated with raw water using formazine as a standard substance. Although the details of this phenomenon are unknown, formazin has a relatively narrow particle size distribution,
When grasping the rejection of particles having a particle size of 0 μm or less, the rejection for each particle size could be evaluated more clearly than other standard substances. It is considered that the effect of the small particle size is small.
【0028】[0028]
【表1】 [Table 1]
【表2】 [Table 2]
【0029】[0029]
【発明の効果】上記の構成とすることにより、本発明
は、高粒径の粒子の影響を受けずに低粒径粒子の分離性
能を評価することができるという効果を奏する。With the above arrangement, the present invention has an effect that the performance of separating small particles can be evaluated without being affected by high particles.
【図1】本発明の分離性能評価方法に使用する装置の一
例を示す概略図である。FIG. 1 is a schematic diagram showing an example of an apparatus used for a separation performance evaluation method of the present invention.
【図2】実施例に示す各標準物質の粒子径と数平均阻止
率を示すグラフである。FIG. 2 is a graph showing the particle diameter and the number average rejection of each standard substance shown in Examples.
1:上部ろ過器 2:ろ過布 3:ろ過布支持台 4:下部ろ過台 5:ゴム栓 6:金属製クランプ 7:吸引瓶 8:メスシリンダー 1: Upper filter 2: Filter cloth 3: Filter cloth support stand 4: Lower filter stand 5: Rubber stopper 6: Metal clamp 7: Suction bottle 8: Measuring cylinder
Claims (6)
平均粒子径が1μm以上5μm以下の懸濁粒子を使用す
ることを特徴とする懸濁物質の分離性能評価方法。(1) In evaluating the separation performance of a suspended substance,
A method for evaluating the performance of separating suspended substances, wherein suspended particles having an average particle diameter of 1 μm or more and 5 μm or less are used.
して、布帛からなるろ過布を用いることを特徴とする請
求項1記載の懸濁物質の分離性能評価方法。2. The method for evaluating the separation performance of a suspended substance according to claim 1, wherein a filter cloth made of a cloth is used as the filtering means for evaluating the separation performance of the suspended substance.
なるろ過層を有する布帛であることを特徴とする請求項
2記載の懸濁物質の分離性能評価方法。3. The method for evaluating the performance of separating suspended substances according to claim 2, wherein the filter cloth is a cloth having a filter layer made of ultrafine fibers of 0.1 to 10 μm.
徴とする請求項1〜3のいずれかに記載の懸濁物質の分
離性能評価方法。4. The method according to claim 1, wherein the suspended particles are made of a fine mineral.
とする請求項4記載の懸濁物質の分離性能評価方法。5. The method according to claim 4, wherein the fine mineral is kaolin.
徴とする請求項1〜3のいずれかに記載の懸濁物質の分
離性能評価方法。6. The method according to claim 1, wherein the suspended particles are formazine.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20431097A JPH1147629A (en) | 1997-07-30 | 1997-07-30 | Method for evaluating separation performance of suspended solids |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20431097A JPH1147629A (en) | 1997-07-30 | 1997-07-30 | Method for evaluating separation performance of suspended solids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH1147629A true JPH1147629A (en) | 1999-02-23 |
Family
ID=16488374
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20431097A Pending JPH1147629A (en) | 1997-07-30 | 1997-07-30 | Method for evaluating separation performance of suspended solids |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH1147629A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006095406A (en) * | 2004-09-29 | 2006-04-13 | Toray Ind Inc | MEMBRANE FILTERING EVALUATION METHOD AND DEVICE, AND MEMBRANE SEPARATION METHOD AND DEVICE |
-
1997
- 1997-07-30 JP JP20431097A patent/JPH1147629A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006095406A (en) * | 2004-09-29 | 2006-04-13 | Toray Ind Inc | MEMBRANE FILTERING EVALUATION METHOD AND DEVICE, AND MEMBRANE SEPARATION METHOD AND DEVICE |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Eyvaz et al. | Textile Materials in Liquid Filtration Practices: Current Status and Perspectives in Water and Wastewater | |
| EP0904819A1 (en) | Pleats filter | |
| WO2006057726A1 (en) | Composite filtration media | |
| US6241879B1 (en) | Filtering machine and filter cloth therefor | |
| CA2018867A1 (en) | Organic microfibrilated material for filter | |
| KR20140035395A (en) | Liquid filtration media | |
| JPS6213046B2 (en) | ||
| NO792803L (en) | THREE-DIMENSIONAL FILTER ELEMENTS OF A TEXTILE FLAT STRUCTURE | |
| JP3385824B2 (en) | Composite membrane | |
| JP3146891B2 (en) | Filter cloth | |
| WO2017055638A1 (en) | Filter medium having excellent heat resistance | |
| US4289627A (en) | Liquid filtration process | |
| JP2012040526A (en) | Filter for liquid filtration, and liquid filtration method | |
| Sakpal et al. | Application of nonwovens for water filtration | |
| DE60035597T2 (en) | FILTER CLOTH AND REPLACEABLE FILTER MODULE | |
| JPH09313832A (en) | High-performance filter cloth | |
| JPS6363311B2 (en) | ||
| JP3144246B2 (en) | Filter cloth | |
| JPH08192017A (en) | Durability improvement filter cloth | |
| JP2003129393A (en) | Organic ultra-fine fiber sheet | |
| JP5530249B2 (en) | Filter media and cartridge filter for liquid filters | |
| JP2000262819A (en) | Filter cloth and solid-liquid separator | |
| JPH0534733Y2 (en) | ||
| JP2000218111A (en) | Filter cloth and method for producing the same | |
| RU2157274C1 (en) | Filtering material |