JPH04193315A - Filter having porous layer - Google Patents
Filter having porous layerInfo
- Publication number
- JPH04193315A JPH04193315A JP32260390A JP32260390A JPH04193315A JP H04193315 A JPH04193315 A JP H04193315A JP 32260390 A JP32260390 A JP 32260390A JP 32260390 A JP32260390 A JP 32260390A JP H04193315 A JPH04193315 A JP H04193315A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- filter medium
- nonwoven fabric
- porous
- layer
- 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
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 44
- 239000011347 resin Substances 0.000 claims abstract description 37
- 229920005989 resin Polymers 0.000 claims abstract description 37
- 239000000463 material Substances 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000007787 solid Substances 0.000 claims abstract description 10
- 238000005187 foaming Methods 0.000 claims abstract description 8
- 230000035699 permeability Effects 0.000 claims abstract description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 4
- 229920002472 Starch Polymers 0.000 claims abstract description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 4
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims abstract description 4
- 239000008107 starch Substances 0.000 claims abstract description 4
- 235000019698 starch Nutrition 0.000 claims abstract description 4
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 3
- 239000006260 foam Substances 0.000 claims description 22
- 239000003292 glue Substances 0.000 claims description 7
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 6
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 6
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 6
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 6
- 239000000853 adhesive Substances 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 229940068984 polyvinyl alcohol Drugs 0.000 claims description 3
- 229920005992 thermoplastic resin Polymers 0.000 claims description 3
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 2
- 229940105329 carboxymethylcellulose Drugs 0.000 claims description 2
- 239000000661 sodium alginate Substances 0.000 claims description 2
- 235000010413 sodium alginate Nutrition 0.000 claims description 2
- 229940005550 sodium alginate Drugs 0.000 claims description 2
- 229940080313 sodium starch Drugs 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 abstract description 18
- 239000002699 waste material Substances 0.000 abstract description 11
- 239000010419 fine particle Substances 0.000 abstract description 6
- 239000004744 fabric Substances 0.000 abstract description 3
- 229920001169 thermoplastic Polymers 0.000 abstract 1
- 239000004416 thermosoftening plastic Substances 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 23
- 238000001914 filtration Methods 0.000 description 20
- 230000000052 comparative effect Effects 0.000 description 11
- 239000011148 porous material Substances 0.000 description 11
- 239000012530 fluid Substances 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 238000005259 measurement Methods 0.000 description 6
- -1 polyethylene terephthalate Polymers 0.000 description 6
- 238000003754 machining Methods 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000691 measurement method Methods 0.000 description 3
- 229940047670 sodium acrylate Drugs 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 238000009423 ventilation Methods 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 229940088990 ammonium stearate Drugs 0.000 description 2
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229940099112 cornstarch Drugs 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000009760 electrical discharge machining Methods 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000011491 glass wool Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940032147 starch Drugs 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000009763 wire-cut EDM Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、工業用濾材に関するものであり、特に固液分
離用濾材、なかんずくワイヤーカット用として好適な濾
材に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to an industrial filter medium, and particularly to a filter medium suitable for solid-liquid separation, particularly for wire cutting.
[従来の技術)
従来、金属切削、特にワイヤーカット放電加工は細いワ
イヤーを電極として、ワイヤーにテンションをかけなが
ら巻取り、ワイヤーと被加工物の間に放電を発生させ、
この放電エネルギによって被加工物を加工するものであ
る。この際、生じる加工屑は清浄水によって噴射洗浄さ
れる。この加工屑を含んだ水をポンプでフィルターに送
りフィルタ中の濾材で濾過を行ない、清滲槽へ送る。清
浄漕で清浄にされた加工液はポンプで加工槽に送られる
ように循環している。[Conventional technology] Conventionally, metal cutting, especially wire-cut electrical discharge machining, uses a thin wire as an electrode, winds the wire while applying tension, and generates an electrical discharge between the wire and the workpiece.
The workpiece is machined using this discharge energy. At this time, the generated processing waste is sprayed and washed with clean water. This water containing processing waste is sent to a filter by a pump, filtered by a filter medium in the filter, and sent to a clarification tank. The processing fluid that has been purified in the cleaning tank is circulated by a pump and sent to the processing tank.
上記放電加工屑は被加工物、電極の消耗したもので、直
径2〜3薗程度から極微小な粒子までばらついている。The electrical discharge machining waste is the worn out workpiece or electrode, and varies in diameter from about 2 to 3 mm to extremely small particles.
濾過には捕集すべき最小粒径、圧損、濾材の寿命が大切
であるが、この3点を満足させるためには濾過面積を大
きく、濾過速度を小さく濾材の開孔径を小さくする必要
がある。このため例えば、フィルターとしてひだ状にし
て麦面積を大きくした濾布の表面に酸性白土、活性白土
の層を股はす、又ロックウール、ガラスウール、セラミ
ックフィルタ、紙フィルタ等を使用している。近年不織
布も用いられている。For filtration, the minimum particle size to be collected, the pressure drop, and the life of the filter medium are important, but in order to satisfy these three points, it is necessary to increase the filtration area, reduce the filtration speed, and reduce the pore size of the filter medium. . For this purpose, for example, as a filter, a layer of acid clay or activated clay is placed on the surface of a filter cloth made into pleats to increase the wheat area, or rock wool, glass wool, ceramic filters, paper filters, etc. are used. . In recent years, nonwoven fabrics have also been used.
[発明が解決しようをする課題]
不縁布製フィルタは、濾過効率が高く圧力損失も少ない
が、それでも微粒子により目詰まりを起こしている。こ
れを改良したものにスパンボンド不織布を積層して多層
構造にし、ニードリングを施し、表皮層から加圧して表
面を密な構造にするものも開発されている。[Problems to be Solved by the Invention] Filters made of non-woven fabric have high filtration efficiency and low pressure loss, but are still prone to clogging due to fine particles. An improved version of this has also been developed in which spunbond nonwoven fabric is laminated to create a multilayer structure, which is then subjected to needling and pressure is applied from the epidermal layer to create a dense surface structure.
しかしながら、この構造のフィルターにおいても、従来
の不織布フィルターよりも寿命が延びるものの、ワイヤ
ーカット放電加工に上記不織布フィルターを用いる場合
、加工液の粒子径分布が大きいため、加工液中の超微細
な加工屑までが主に不織布表面で捕捉されて目詰まりを
起し、濾過が進行するに伴って急速に圧力損失が大きく
なる。However, although filters with this structure have a longer service life than conventional non-woven fabric filters, when using the above-mentioned non-woven fabric filters for wire-cut electric discharge machining, the particle size distribution of the machining fluid is large, so ultra-fine machining in the machining fluid is difficult. Even debris is mainly captured on the surface of the nonwoven fabric, causing clogging, and pressure loss rapidly increases as filtration progresses.
また初期には加工液中の微粒子の加工屑は主に不織布表
面で捕捉されないという欠点があった。In addition, in the early stages, there was a drawback that processing debris in the form of fine particles in the processing fluid was not primarily captured on the surface of the nonwoven fabric.
本発明は上記従来の欠点、課題を克服するものであり、
加工液中の微粒子の加工屑も捕捉するように、濾材の透
過孔径を小さくし、且つフィルタの目詰まりを防止し濾
過液体の圧力損失を押さえることにより長寿命の濾材を
得ることを目的とするものである。The present invention overcomes the above-mentioned conventional drawbacks and problems,
The purpose is to obtain a long-life filter material by reducing the permeation pore diameter of the filter material so as to capture processing waste particles in the processing fluid, preventing clogging of the filter, and suppressing the pressure loss of the filtered fluid. It is something.
;課題を解決するための手段]
本発明は上記目的を達成するために、不織布の片面に通
水性を有する多孔性樹脂層を形成せしめたことを特徴と
する多孔層を有する濾材、目付10〜1000g#rf
の不織布の片面に不織布重量の0.5〜80%の通水性
を有する多孔性樹脂層を形成せしめた多孔層を育する濾
材、多孔性樹脂層は、樹脂を機械発泡又は化学発泡して
なる連続発泡体であり、多孔性樹脂層を形成する樹脂は
、熱可塑性樹脂又は熱硬化性樹脂1、好ましくは熱可塑
性樹脂であり、該樹脂中に易水溶性の糊材を添加する。;Means for Solving the Problems] In order to achieve the above object, the present invention provides a filter material having a porous layer, characterized in that a porous resin layer having water permeability is formed on one side of a nonwoven fabric, and a filter material having a basis weight of 10 to 1000g#rf
A filter material for growing a porous layer in which a porous resin layer having a water permeability of 0.5 to 80% of the weight of the nonwoven fabric is formed on one side of a nonwoven fabric, and the porous resin layer is formed by mechanically foaming or chemically foaming the resin. The resin forming the porous resin layer of the open foam body is a thermoplastic resin or a thermosetting resin 1, preferably a thermoplastic resin, and an easily water-soluble glue material is added to the resin.
易水溶性糊材は、ポリビニールアルコール、カルボキシ
ルメチルセルロース、アルギン酸ソーダ又は澱粉及びこ
れらの同効物であり、易水溶性糊材は、樹脂の固形分に
対して0.05〜50重量%添加した多孔層を有する濾
材に構成するものである。The easily water-soluble adhesive material is polyvinyl alcohol, carboxymethyl cellulose, sodium alginate, starch, or equivalent substances thereof, and the easily water-soluble adhesive material is added in an amount of 0.05 to 50% by weight based on the solid content of the resin. The filter medium has a porous layer.
本発明の連続発泡体からなる濾材の表層では加工液中の
加工屑を捕捉してケーキが形成され、ケーキが濾過作用
をする。一定量以上のケーキが濾材の表層に堆積すると
圧力損失が急激に上昇する。The surface layer of the filter medium made of the open foam of the present invention traps processing debris in the processing fluid to form a cake, and the cake performs a filtering action. When more than a certain amount of cake accumulates on the surface layer of the filter medium, the pressure loss increases rapidly.
一方、微粒子の加工屑は発泡体の孔に捕捉され目詰りが
生じるが、時間の経過と共に発泡体中の易水溶性糊材が
溶解することにより新たな通水孔が形成されるというこ
とを繰り返すため、目詰まりを起しにくく、圧力損失が
大きくなるこ2はなく濾過流量が大きく濾過効率が良い
。即ち、濾材の寿命が長くなる。On the other hand, fine particles of processing debris are trapped in the pores of the foam and cause clogging, but as time passes, the easily water-soluble glue in the foam dissolves, forming new water holes. Because it is repeated, clogging is less likely to occur, pressure loss does not increase, the filtration flow rate is large, and filtration efficiency is high. That is, the life of the filter medium becomes longer.
以下、本発明の実施例を図面とともに説明する。 Embodiments of the present invention will be described below with reference to the drawings.
第1図は本発明の濾材の概略平面図、第2図はその概略
縦断面図であり、(1)は連続発泡体層、(2)は発泡
体であり、(3)は樹脂中に溶解している易水溶性糊材
、(4)は不織布層である。Fig. 1 is a schematic plan view of the filter medium of the present invention, and Fig. 2 is a schematic longitudinal cross-sectional view thereof, in which (1) is an open foam layer, (2) is a foam, and (3) is a resin layer. The dissolved easily water-soluble glue material (4) is a nonwoven fabric layer.
不織布の素材は特に限定されない。天然繊維でも合成繊
維でもよいが、濾材の耐久性の点から、所謂スパンボン
ド法により製造供給することが好ましいが、他の不縁布
製造法によることも差し支えない。The material of the nonwoven fabric is not particularly limited. Although natural fibers or synthetic fibers may be used, from the viewpoint of durability of the filter medium, it is preferable to manufacture and supply the filter medium by a so-called spunbond method, but other non-woven fabric manufacturing methods may also be used.
そしてその構成繊維は、汎用のポリエステル(ポリエチ
レンテレフタレート、ポリブチレンテレフタレート等)
及びそのコポリマー、ポリアマイド(ナイロン6、ナイ
ロン66等)及びそのコポリマー、ポリプロピレン等が
好適であるが、汎用合成繊維であればいずれでもよい。Its constituent fibers are general-purpose polyesters (polyethylene terephthalate, polybutylene terephthalate, etc.)
and copolymers thereof, polyamides (nylon 6, nylon 66, etc.) and copolymers thereof, polypropylene, etc. are suitable, but any general-purpose synthetic fiber may be used.
不織布の製造方法としては、ウェブを部分的に熱圧着し
たりあるいは常用のニードルパンチング法であってもよ
く、ウォータージェット交絡法により交絡し一体化する
方法であってもよい。ここでウォータージェット交絡法
とは、例えばNonwovens world 3 N
o、2.p、62〜63(March 1981t)に
も紹介されている。The nonwoven fabric may be produced by partially thermocompressing the web, by a commonly used needle punching method, or by entangling and integrating the web by a water jet entangling method. Here, the water jet entangling method is, for example, Nonwovens world 3 N
o, 2. Also introduced in p. 62-63 (March 1981t).
不織布の厚さは0.1〜10mn程度であり、その目付
量は10〜1000g/rriとする。The thickness of the nonwoven fabric is about 0.1 to 10 mm, and the basis weight is 10 to 1000 g/rri.
次いで、不織布をアクリル等の合成樹脂液に含浸して加
熱ローラ間でニップし余剰樹脂液を絞り、ついで乾燥し
て、保形性、強靭性、濾過性を付与する。Next, the nonwoven fabric is impregnated with a synthetic resin liquid such as acrylic, nipped between heating rollers to squeeze out excess resin liquid, and then dried to impart shape retention, toughness, and filterability.
その後、機械発泡可能なエマルジョン状態の樹脂、水溶
性樹脂、整泡剤及び増粘剤を混合してコーテイング液を
調整した。エマルジョンを形成することができる樹脂と
して、酢酸ビニール、塩化ビニール、アクリル酸エステ
ル、メチルメタアクリレート−アクリル酸エステル共重
合体、その他ポリエステル系、ポリウレタン系、ポリア
ミド系の樹脂又はゴムとこれらの共重合体であってもよ
い。水溶性樹脂としては、例えばポリビニルアルコール
、カルボキシルメチルセルロース、でん粉。Thereafter, a mechanically foamable emulsion resin, a water-soluble resin, a foam stabilizer, and a thickener were mixed to prepare a coating liquid. Examples of resins that can form emulsions include vinyl acetate, vinyl chloride, acrylic esters, methyl methacrylate-acrylic ester copolymers, other polyester-based, polyurethane-based, polyamide-based resins or rubbers, and copolymers thereof. It may be. Examples of water-soluble resins include polyvinyl alcohol, carboxymethyl cellulose, and starch.
デキストリン、ポリアクリル酸アミド、メチルセルロー
ス、カゼイン等が使用される。整泡剤としては、高級脂
肪酸塩、例えばステアリン酸アンモン等、増粘剤として
はアクリル酸ソーダ等が選ばれる。Dextrin, polyacrylic acid amide, methylcellulose, casein, etc. are used. As the foam stabilizer, higher fatty acid salts such as ammonium stearate are selected, and as the thickener, sodium acrylate and the like are selected.
上記のコーテイング液はオークスミキサ−等により機械
発泡を行い、得られた組成物を対不織布重量で0.5〜
80%、好ましくは5〜10%を不織布の片面に撒布し
、乾燥する。発泡組成物の発泡倍率は孔径等を考慮して
1.5〜5倍程度が好適である。その後発泡樹脂層の表
面をロールで加圧してもよい。このようにして濾材の圧
力損失を高めないように通水性を有する多孔層で表面平
滑な連続発泡体を表層に備えた濾材(5)が形成される
。The above coating liquid is mechanically foamed using an oak mixer or the like, and the resulting composition is 0.5 to 0.5 to
80%, preferably 5-10%, is spread on one side of the non-woven fabric and dried. The foaming ratio of the foaming composition is preferably about 1.5 to 5 times, taking into account the pore diameter and the like. Thereafter, the surface of the foamed resin layer may be pressed with a roll. In this way, a filter medium (5) is formed which has a porous layer having water permeability and an open foam with a smooth surface on its surface so as not to increase the pressure loss of the filter medium.
濾材は第3図及び第4図に示すように使用される。第3
図は本発明の一実施例を示す濾材を収容した収容体の斜
視図、第4図は同断面図である。The filter media is used as shown in FIGS. 3 and 4. Third
The figure is a perspective view of a container housing a filter medium according to an embodiment of the present invention, and FIG. 4 is a sectional view thereof.
収容体(6)は円筒状に形成した枠体(7)からなり、
収容体(6)の内部に濾材(5)を挿入して固定し、濾
材(5)の中心部に孔(8)を有するシリンダ(9)を
挿入する。濾材(5)はジャバラ状に記数し、濾過面積
を大きくする。加工液は、枠体(7)の外側から濾材(
5)を通過して加工屑を濾過しながらシリンダ(9)へ
流入してもよいし、逆にシリンダ(9)から外側に流出
して濾材(5)を通過して加工屑を濾過しながら枠体(
7)の外側へ流出させるようにしてもよい。The container (6) consists of a cylindrical frame (7),
A filter medium (5) is inserted and fixed inside the container (6), and a cylinder (9) having a hole (8) is inserted into the center of the filter medium (5). The filter medium (5) is numbered in a bellows shape to increase the filtration area. The machining liquid flows from the outside of the frame (7) to the filter medium (
5) may flow into the cylinder (9) while filtering the processed waste, or conversely, it may flow out from the cylinder (9) to the outside and pass through the filter medium (5) while filtering the processed waste. Frame (
7) may be made to flow outside.
実施例1 以下、実施例をもって本発明を具体的に説明する。Example 1 The present invention will be specifically explained below with reference to Examples.
不織布として目付150g/mのポリエステルスパンボ
ンド不織布を用い、30本/ cntの密度でニードリ
ングを施し、次いで不織布をアクリル樹脂液に含浸した
後、加熱ローラでニップし、乾燥した。その後、固形分
50%のアクリル酸エステル77重量部に、固形分2%
のカルボキシルメチルセルロースを15重量部、整泡剤
として固形分30%のステアリン酸アンモニウムを5重
量部、増粘剤として固形分30%のアクリル酸ソーダを
3重量部添加し、粘度8000cpsに調整した。A polyester spunbond nonwoven fabric with a basis weight of 150 g/m was used as the nonwoven fabric, and needling was performed at a density of 30 threads/cnt.The nonwoven fabric was then impregnated with an acrylic resin liquid, and then nipped with heated rollers and dried. Then, 77 parts by weight of acrylic ester with a solid content of 50% was added with a solid content of 2%.
15 parts by weight of carboxymethylcellulose (15 parts by weight), 5 parts by weight of ammonium stearate (30% solid content) as a foam stabilizer, and 3 parts by weight of sodium acrylate (30% solid content) as a thickener were added to adjust the viscosity to 8000 cps.
これを混合した混合液をオークスミキサニで機械発泡を
行い、発泡倍率4倍に調整した。この発泡組成物を対不
織布重量で7%にしてDry20g/m2に調整し、ポ
リエステルスパンボンド不織布の片面に20m/分の送
り速度でナイフコートし、150℃で加熱して発泡層の
気泡を連続発泡に成形した。The mixed solution was mechanically foamed using an oak mixer, and the foaming ratio was adjusted to 4 times. This foam composition was adjusted to 7% by weight of the non-woven fabric to dry 20 g/m2, knife-coated on one side of the polyester spunbond non-woven fabric at a feed rate of 20 m/min, and heated at 150°C to make the cells in the foam layer continuous. Molded into foam.
比較例1
不縁布として日付150g/lrfのポリエステルスパ
ンボンド不織布を用い、30本/dの密度でニードリン
グを施し、次いで不織布をアクリル樹脂液に含浸した後
、加熱ローラでニップし、乾燥した。その後、固形分5
0%のアクリル酸エステル77重量部に、固形分2%の
カルボキシルメチルセルロースを15重量部、増粘剤と
して固形分30%のアクリル酸ソーダを3重量部添加し
、粘度8000cpsに調整した。これを混合した混合
液を対不織布重量で7%にしてDry20 g / r
rfに調整し、ポリエステルスパンボンド不織布の片面
に20m/分の送り速度でナイフコートし、150℃で
加熱して成形した。Comparative Example 1 A polyester spunbond nonwoven fabric with a date of 150g/lrf was used as the nonwoven fabric, and needling was performed at a density of 30 threads/d.Then, the nonwoven fabric was impregnated with an acrylic resin liquid, and then nipped with heating rollers and dried. . After that, solid content 5
To 77 parts by weight of 0% acrylic ester, 15 parts by weight of carboxymethyl cellulose with a solid content of 2% and 3 parts by weight of sodium acrylate with a solid content of 30% as a thickener were added, and the viscosity was adjusted to 8000 cps. Dry20 g/r by mixing this mixture to 7% by weight of the nonwoven fabric.
RF, one side of the polyester spunbond nonwoven fabric was coated with a knife at a feed rate of 20 m/min, and was heated and molded at 150°C.
比較例2
不織布として日付150g/rdのポリエステルスパン
ボンド不織布を用い、30本/cI11の密度でニード
リングを施し、次いで不織布をアクリル樹脂液に含浸し
た後、加熱ローラでニップし、乾燥した濾材を構成した
。Comparative Example 2 A polyester spunbond nonwoven fabric with a date of 150g/rd was used as the nonwoven fabric, and needling was performed at a density of 30 pieces/cI11.Then, the nonwoven fabric was impregnated with an acrylic resin liquid, and then nipped with a heating roller, and the dried filter medium was Configured.
比較例3
不織布として日付270g/rrfのポリエステルスパ
ンボンド不織布にアクリル樹脂液を塗布した後、模様ロ
ールで熱圧着し部分的に不織布をフィルム化した他社の
製品を得た。Comparative Example 3 A product manufactured by another company was obtained by applying an acrylic resin liquid to a polyester spunbond nonwoven fabric with a date of 270 g/rrf as a nonwoven fabric, and then thermally pressing the fabric with a patterned roll to partially form a film from the nonwoven fabric.
比較例4
孔径30〜60 μm、 B付150g/rrfのパル
プ紙にコーンスターチ糊の水溶液を通過させた後。Comparative Example 4 After passing an aqueous solution of cornstarch glue through a pulp paper with a pore diameter of 30 to 60 μm and a B attachment of 150 g/rrf.
エポキシ樹脂を上布し過熱乾燥した厚さ0. 5mmの
他社の濾紙を得た。Thickness: 0.0mm thick coated with epoxy resin and dried by heating. A 5 mm filter paper made by another company was obtained.
上記実施例1、比較例1.3における各不織布の物性に
ついて下記のような結果をえた。The following results were obtained regarding the physical properties of each nonwoven fabric in Example 1 and Comparative Examples 1.3.
表1 物性の測定方法 − 目付はJIS L−1085−5,2によった。Table 1 Method of measuring physical properties - The basis weight was based on JIS L-1085-5,2.
厚さはダイヤルシンクネスゲージによりI、65ctj
の試料に50gの荷重をかけて測定した。Thickness is I, 65ctj by dial sinkness gauge
The measurement was performed by applying a load of 50 g to the sample.
引張強力及び伸度はJ I S’ L−1085−5゜
2、引裂強力はJ’IS L−1085−5,5C法に
よった。Tensile strength and elongation were determined by JIS L-1085-5°2, and tear strength was determined by J'IS L-1085-5,5C method.
乾熱収縮は25cmX25cmの試料に縦、横各々3個
所に正確に長さを表す印を付け、恒温乾燥機内で180
℃で3分放置した後、試料を取り比して室温まで冷却し
た。ついで、前記印を付けた乾燥前後の長さ変化を測定
した。For dry heat shrinkage, mark a 25cm x 25cm sample accurately in three places each vertically and horizontally, and heat it to 180cm in a constant temperature dryer.
After being left at ℃ for 3 minutes, the sample was removed and cooled to room temperature. Next, the change in the length of the marked pieces before and after drying was measured.
試料5%及び3%伸長時応力はJISL−1096によ
った。The stress at 5% and 3% elongation of the sample was based on JISL-1096.
また比較例4における不織布の物性について下記のよう
な結果をえた。Furthermore, the following results were obtained regarding the physical properties of the nonwoven fabric in Comparative Example 4.
表 2
上記測定方法において、目付及び厚さはJISP−81
,’88、破裂強度はJIS P−8112(シュー
シン法)、引張強度は、ll5P−8113によった。Table 2 In the above measurement method, the basis weight and thickness are determined according to JISP-81.
, '88, bursting strength was determined according to JIS P-8112 (Shushin method), and tensile strength was determined according to 115P-8113.
上記測定結果から実施例1による不織布の片面に通水性
を有する多孔性樹脂層を形成せしめても諸物性の低下が
みられなかった。From the above measurement results, even when a porous resin layer having water permeability was formed on one side of the nonwoven fabric according to Example 1, no deterioration in physical properties was observed.
またポアサイズ及び通気抵抗について測定した結果は下
記のとおりである。In addition, the results of measurements regarding pore size and ventilation resistance are as follows.
表3
上記測定方法において、ポアサイズは東洋濾紙製Bub
ble試験器、通気抵抗は東洋製作新製のNo、869
通気抵抗試験器によった。Table 3 In the above measurement method, the pore size was measured using Toyo Roshi Bub
BLE tester, ventilation resistance is No. 869 manufactured by Toyo Seisakusho.
Using an airflow resistance tester.
上記測定結果から実施例1による濾材はポアサイズが比
較例1に比べて小さいにも拘らず通気抵抗は格段に大き
いことが判明した。The above measurement results revealed that although the filter medium of Example 1 had a smaller pore size than that of Comparative Example 1, its ventilation resistance was significantly higher.
また濾過性能についても比較測定した。測定結果は下記
の表に示すとおりである。Comparative measurements were also made regarding filtration performance. The measurement results are shown in the table below.
表4
濾過性能の測定法
試験粉体としてJIS Z8901に規定するJIS
8種(日本粉体工業技術協会の標準粉体)を使用し、受
水槽の被試験液体を初期流量17Q/ m i nで被
検濾過体中の濾過面積0.217rrfを有する濾材に
より濾過させる。被試験液体には10gまでは3分毎に
1gの試験粉体を投入し、10g以上になったら、その
後は3分毎に3gの試験粉体を投入する。濾液と試験粉
体投入前の試験液の濁度を濁度計で測定し、同者の濁度
が一致した時の試験粉体膜大量の合計を測定し、清澄点
とする。Table 4 Filtration performance measurement method JIS specified in JIS Z8901 as test powder
Using 8 types (standard powder of Japan Powder Industry Technology Association), the test liquid in the water tank is filtered through a filter medium having a filtration area of 0.217rrf in the test filter at an initial flow rate of 17Q/min. . 1 g of test powder is added to the liquid to be tested every 3 minutes up to 10 g, and after that, 3 g of test powder is added every 3 minutes after reaching 10 g. Measure the turbidity of the filtrate and the test liquid before adding the test powder using a turbidity meter, and when the turbidities of the same turbidity match, measure the total amount of the test powder film and use it as the clearing point.
また初期流量17 Q /minが半減し、8.5Q/
m1nになった時の試験粉体の合計投入量を測定し、ラ
イフとする。In addition, the initial flow rate of 17Q/min was halved to 8.5Q/min.
The total amount of test powder input when it reaches m1n is measured and taken as the life.
早く清澄するほど清澄点は小さく、濾過精度がよい。ま
た、ライフは長いほど商品価値が高い。The faster the water is clarified, the smaller the fining point and the better the filtration accuracy. Also, the longer the life, the higher the product value.
この結果から明らかなように、実施例1は比較例1〜4
に比べて早く清澄し、比較例3,4に比べてライフが長
い。As is clear from this result, Example 1 is different from Comparative Examples 1 to 4.
It clears faster than Comparative Examples 3 and 4, and has a longer life than Comparative Examples 3 and 4.
[発明の効果]
本発明は上記のように構成したので、加工液中の加工屑
は孔径の小さい連続発泡体層上で充分捕捉されるので、
徐々にケーキが連続発泡体層の上に形成されて堆積し、
その結果、大きい加工屑はケーキで捕捉され、小さい加
工屑は連続発泡体層で捕捉され、濾過作用が好適に進行
する。一方、微粒子の加工屑は発泡体の孔に捕捉され目
詰りが生じるが、時間の経過と共に連続発泡体中のカル
ボキシルメチルセルロース等の易水溶性糊材が溶解して
海綿状になり新たな濾過孔が形成されるので、新たに形
成された濾過孔で加工液中の加工屑が捕捉され、目詰ま
りを生じることなく、濾過作用が進行するので、濾材の
寿命を延長することができる。一方、本体層の不織布層
は、ケーキの形成による濾材の肉厚に耐える補強効果を
有するとともに、ケーキの剥離も好適に行なわれ、ニー
ドリングと樹脂加工により成形性を有するので、形崩れ
を生じることがない。そして、スパンボンドの網目状積
層が機械的強度を確保し、強靭である。[Effects of the Invention] Since the present invention is constructed as described above, processing debris in the processing fluid is sufficiently captured on the open foam layer with small pore diameters.
Gradually a cake forms and deposits on top of the open foam layer,
As a result, large processing wastes are captured by the cake, small processing wastes are captured by the continuous foam layer, and the filtration action progresses suitably. On the other hand, fine particles of processing debris are trapped in the pores of the foam and cause clogging, but as time passes, easily water-soluble glue materials such as carboxymethyl cellulose in the open foam dissolve and become spongy, creating new filtration pores. is formed, processing debris in the processing liquid is captured by the newly formed filter holes, and the filtering action proceeds without clogging, thereby extending the life of the filter medium. On the other hand, the nonwoven fabric layer of the main body layer has a reinforcing effect that can withstand the thickness of the filter medium due to the formation of a cake, and the cake can be peeled off properly, and it has moldability through needling and resin processing, so it does not lose its shape. Never. The spunbond mesh layer ensures mechanical strength and is tough.
このように、本発明の濾材は加工屑の濾過効率が向上し
、清澄点が速く、濾過精度がよいと共に濾材の寿命が長
く、商品価値が高められた。また、連続発泡体の表面に
樹脂加工を施しているので、ケーキの剥離性に優れ、再
使用時にケーキによる目詰まりを生じることがない。As described above, the filter medium of the present invention has improved filtration efficiency of processing waste, has a fast fining point, has good filtration accuracy, has a long life span, and has increased commercial value. Furthermore, since the surface of the open foam is treated with resin, it has excellent cake removability and does not cause clogging due to cake when reused.
第1図は本発明の一実施例を示す濾材の概略平面図、第
2図は同概略断面拡大図、第3図は本発明の一実施例を
示す濾材を収容した濾過体の斜視図、第4図は同一部断
面側面図である。
に連続発泡体層 2:発泡体
3:易水溶性糊材 4:不織布層5:濾材′
6:収容体7:枠体
8:孔
9ニジリンダFIG. 1 is a schematic plan view of a filter medium showing an embodiment of the present invention, FIG. 2 is a schematic enlarged cross-sectional view of the same, and FIG. 3 is a perspective view of a filter body containing a filter medium showing an embodiment of the present invention. FIG. 4 is a partially sectional side view of the same. Continuous foam layer 2: Foam 3: Easily water-soluble adhesive 4: Nonwoven fabric layer 5: Filter medium'
6: Container 7: Frame
8: Hole 9 Nijilinda
Claims (6)
成せしめたことを特徴とする多孔層を有する濾材。(1) A filter medium having a porous layer, characterized in that a porous resin layer having water permeability is formed on one side of a nonwoven fabric.
不織布重量の0.5〜80%の通水性を有する多孔性樹
脂層を形成せしめたことを特徴とする請求項(1)記載
の多孔層を有する濾材。(2) A porous resin layer having a water permeability of 0.5 to 80% of the weight of the nonwoven fabric is formed on one side of the nonwoven fabric having a basis weight of 10 to 1000 g/m^2. A filter medium with a porous layer.
てなる連続発泡体であることを特徴とする請求項(1)
又は(2)記載の多孔層を有する濾材。(3) Claim (1) characterized in that the porous resin layer is an open foam formed by mechanically foaming or chemically foaming a resin.
Or a filter medium having a porous layer according to (2).
は熱硬化性樹脂であり、該樹脂中に易水溶性の糊材を添
加することを特徴とする請求項(1)、(2)又は(3
)記載の多孔層を有する濾材。(4) The resin forming the porous resin layer is a thermoplastic resin or a thermosetting resin, and an easily water-soluble glue material is added to the resin. ) or (3
) A filter medium having a porous layer as described above.
ボキシルメチルセルロース、アルギン酸ソーダ又は澱粉
及びこれらの同効物であることを特徴とする請求項(4
)記載の多孔層を有する濾材。(5) Claim (4) characterized in that the easily water-soluble adhesive material is polyvinyl alcohol, carboxymethyl cellulose, sodium alginate, starch, or equivalent substances thereof.
) A filter medium having a porous layer as described above.
〜10重量%添加したことを特徴とする請求項(4)又
は(5)記載の多孔層を有する濾材。(6) Easily water-soluble glue is 0.05% of the solid content of the resin.
The filter medium having a porous layer according to claim 4 or 5, wherein the porous layer is added in an amount of 10% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32260390A JPH04193315A (en) | 1990-11-28 | 1990-11-28 | Filter having porous layer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32260390A JPH04193315A (en) | 1990-11-28 | 1990-11-28 | Filter having porous layer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04193315A true JPH04193315A (en) | 1992-07-13 |
Family
ID=18145555
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32260390A Pending JPH04193315A (en) | 1990-11-28 | 1990-11-28 | Filter having porous layer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04193315A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002239354A (en) * | 2000-12-15 | 2002-08-27 | Japan U-Pica Co Ltd | Frp microfilter medium and its production method |
JP2009022911A (en) * | 2007-07-20 | 2009-02-05 | Chugoku Electric Power Co Inc:The | Dredging wastewater purification system |
JPWO2009017086A1 (en) * | 2007-07-31 | 2010-10-21 | 東レ株式会社 | Separation membrane support and method for producing the same |
JP2015161667A (en) * | 2014-02-28 | 2015-09-07 | 呉羽テック株式会社 | Cesium adsorption sheet and filtration filter for muddy water using the same |
RU2681906C2 (en) * | 2015-07-21 | 2019-03-13 | ФЕДЕРАЛЬНОЕ ГОСУДАРСТВЕННОЕ БЮДЖЕТНОЕ ОБРАЗОВАТЕЛЬНОЕ УЧРЕЖДЕНИЕ ВЫСШЕГО ПРОФЕССИОНАЛЬНОГО ОБРАЗОВАНИЯ "САНКТ-ПЕТЕРБУРГСКИЙ ГОСУДАРСТВЕННЫЙ АГРАРНЫЙ УНИВЕРСИТЕТ" (СПбГАУ) | Method for obtaining filter element based on a porous polyvinylformal |
-
1990
- 1990-11-28 JP JP32260390A patent/JPH04193315A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002239354A (en) * | 2000-12-15 | 2002-08-27 | Japan U-Pica Co Ltd | Frp microfilter medium and its production method |
JP2009022911A (en) * | 2007-07-20 | 2009-02-05 | Chugoku Electric Power Co Inc:The | Dredging wastewater purification system |
JPWO2009017086A1 (en) * | 2007-07-31 | 2010-10-21 | 東レ株式会社 | Separation membrane support and method for producing the same |
JP5724180B2 (en) * | 2007-07-31 | 2015-05-27 | 東レ株式会社 | Separation membrane support and method for producing the same |
JP2015161667A (en) * | 2014-02-28 | 2015-09-07 | 呉羽テック株式会社 | Cesium adsorption sheet and filtration filter for muddy water using the same |
RU2681906C2 (en) * | 2015-07-21 | 2019-03-13 | ФЕДЕРАЛЬНОЕ ГОСУДАРСТВЕННОЕ БЮДЖЕТНОЕ ОБРАЗОВАТЕЛЬНОЕ УЧРЕЖДЕНИЕ ВЫСШЕГО ПРОФЕССИОНАЛЬНОГО ОБРАЗОВАНИЯ "САНКТ-ПЕТЕРБУРГСКИЙ ГОСУДАРСТВЕННЫЙ АГРАРНЫЙ УНИВЕРСИТЕТ" (СПбГАУ) | Method for obtaining filter element based on a porous polyvinylformal |
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